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The Sheahan Diamond Literature Reference Compilation - Scientific and Media Articles based on Major Keyword - Deposits: 2016 onwards
The Sheahan Diamond Literature Reference Compilation is compiled by Patricia Sheahan who publishes on a monthly basis a list of new scientific articles related to diamonds as well as media coverage and corporate announcements called the Sheahan Diamond Literature Service that is distributed as a free pdf to a list of followers. Pat has kindly agreed to allow her work to be made available as an online digital resource at Kaiser Research Online so that a broader community interested in diamonds and related geology can benefit. The references are for personal use information purposes only; when available a link is provided to an online location where the full article can be accessed or purchased directly. Reproduction of this compilation in part or in whole without permission from the Sheahan Diamond Literature Service is strictly prohibited. Return to Diamond Keyword Index
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
Each article reference in the SDLRC is tagged with one or more key words assigned by Pat Sheahan to highlight the main topics of the article. In an effort to make it easier for users to track down articles related to a specific topic, KRO has extracted these key words and developed a list of major key words presented in this Key Word Index to which individual key words used in the article reference have been assigned. In most of the individual Key Word Reports the references are in crhonological order, though in some such as Deposits the order is first by key word and then chronological. Only articles classified as "technical" (mainly scientific journal articles) and "media" (independent media articles) are included in the Key Word Index. References that were added in the most recent monthly update are highlighted in yellow.
The keyword Deposits indicates that the article discusses a particular diamond deposit.
Abstract: Two experimental waste-rock piles (test piles), each 15 m in height × 60 m × 50 m, were constructed at the Diavik diamond mine in Northern Canada to study the behavior of low-sulfide content waste rock, with a similarly low acid-neutralization potential, in a continuous permafrost region. One test pile with an average of 0.035 wt.% S (<50 mm fraction; referred to as Type I) and a second test pile with an average of 0.053 wt.% S (<50 mm fraction; referred to as Type III) were constructed in 2006. The average carbon content in the <50 mm fraction of waste rock in the Type I test pile was 0.031 wt.% as C and in the Type III test pile was 0.030 wt.% as C. The NP:AP ratio, based on the arithmetic mean of particle-size weighted NP and AP values, for the Type I test pile was 12.2, suggesting this test pile was non-acid generating and for the Type III test pile was 2.2, suggesting an uncertain acid-generating potential. The Type I test pile maintained near-neutral pH for the 4-year duration of the study. Sulfate and dissolved metal concentrations were low, with the exception of Ni, Zn, Cd, and Co in the fourth year following construction. The pore water in the Type III test pile contained higher concentrations of SO42? and dissolved metals, with a decrease in pH to <4.7 and an annual depletion of alkalinity. Maximum concentrations of dissolved metals (20 mg L?1 Ni, 2.3 mg L?1 Cu, 3.7 mg L?1 Zn, 35 ?g L?1 Cd, and 3.8 mg L?1 Co) corresponded to decreases in flow rate, which were observed at the end of each field season when the contribution of the total outflow from the central portion of the test pile was greatest. Bacteria were present each year in spite of annual freeze/thaw cycles. The microbial community within the Type I test pile included a population of neutrophilic S-oxidizing bacteria. Each year, changes in the water quality of the Type III test-pile effluent were accompanied by changes in the microbial populations. Populations of acidophilic S-oxidizing bacteria and Fe-oxidizing bacteria became more abundant as the pH decreased and internal test pile temperatures increased. Irrespective of the cold-climate conditions and low S content of the waste rock, the geochemical and microbiological results of this study are consistent with other acid mine drainage studies; indicating that a series of mineral dissolution-precipitation reactions controls pH and metal mobility, and transport is controlled by matrix-dominated flow and internal temperatures.
Canadian Journal of Earth Sciences, Vol. 52, 12, pp. 1169-1181.
Canada, Ontario, Attawapiskat
Deposit - Victor
Abstract: The Moose River Basin in Ontario, Canada, contains nearly 1 km of Silurian marine strata, and although it has been studied for more than a century, its precise correlation globally has not been constrained. Herein, a core from the Victor Mine in the Moose River Basin was examined for conodont biostratigraphy and carbonate carbon (?13Ccarb) isotope chemostratigraphy to provide a detailed chronostratigraphic framework for the Silurian strata (Severn River, Ekwan River, and Attawapiskat formations) in the Moose River Basin. The recovery of Aspelundia expansa, Aspelundia fluegeli fluegeli, Distomodus staurognathoides, Ozarkodina polinclinata estonica, Pterospathodus eopennatus, and Aulacognathus bullatus, as well as the lower Aeronian, upper Aeronian, lower Telychian (Valgu), and ascending limb of the Sheinwoodian (Ireviken) positive carbonate carbon (?13Ccarb) isotope excursions provide significantly improved chronostratigraphic correlation of Llandovery strata in the Moose River Basin.
Silurian Conodont Biostratigraphy and Carbon (?13Ccarb) Isotope Stratigraphy of the Victor Mine (V-03-270-AH) Core in the Moose River Basin.
Abstract: Most kimberlites contain abundant dunitic nodules. These are centimetre-sized, rounded and multi-grained assemblages of xenocrystic olivine with a wide range of compositions (Fo83 to Fo94). The absence of orthopyroxene and other mantle minerals and the range of olivine compositions have been attributed to reaction between mantle peridotite and (proto)kimberlitic fluid or melt, but the timing of the reaction is a subject of debate. In a kimberlite from the Kangamiut region of Greenland, nodule cores are surrounded by fine-grained outer margins with near-constant Fo contents (~Fo88) but highly variable minor element contents (e.g. 500-2500 ppm Ni). These margins crystallized from the kimberlite melt and we show that their compositions can be explained by crystallization of olivine alone, if a high partition coefficient for Ni between melt and olivine (DNi > 20) is assumed. Orthopyroxene assimilation is not required, removing the constraint that its dissolution occurred during ascent of the kimberlite magma. Within some nodules, in addition to the usual core-to-margin gradients, we observe asymmetric compositional changes (variable Fo but near-constant minor element contents) across mobile grain boundaries. These changes document fluid percolation at the grain scale that occurred during dynamic recrystallization in the deforming lithospheric mantle. We note that chemical gradients associated with mobile grain boundaries are observed in olivines that cover the entire compositional range of the nodules, and propose that fluid-assisted dynamic recrystallization took place in dunite that was already compositionally heterogeneous. Reaction between peridotite and protokimberlitic melt or fluid and dissolution of orthopyroxene thus occurred within the lithospheric mantle, immediately (a few days) prior to the ascent of the kimberlite melt and the entrainment of the dunite nodules. We propose that the grain boundary zones probably mimic, at a fine scale, the fluid-peridotite interaction that caused, at a larger scale, orthopyroxene dissolution and formation of compositionally diverse olivine in kimberlites.
Abstract: Kimberlite magmas are of economic and scientific importance because they represent the major host to diamonds and are probably the deepest magmas from continental regions. In addition, kimberlite magmas transport abundant mantle and crustal xenoliths, thus providing fundamental information on the composition of the sub-continental lithosphere. Despite their importance, the composition and ascent mechanism(s) of kimberlite melts remain poorly constrained. Phlogopite is one of the few minerals that preserves a history of fluid migration and magmatism in the mantle and crust and is therefore an invaluable petrogenetic indicator of kimberlite magma evolution. Here we present major and trace element compositional data for phlogopite from the Bultfontein kimberlite (Kimberley, South Africa; i.e. the kimberlite type-locality) and from entrained mantle xenoliths. Phlogopite macrocrysts (~ > 0.3-0.5 mm) and microcrysts (between ~ 0.1 and 0.3 mm) in the Bultfontein kimberlite display concentric compositional zoning patterns. The cores of these phlogopite grains exhibit compositions typical of phlogopite contained in peridotite mantle xenoliths. However, the rims of some grains show compositions analogous to kimberlite groundmass phlogopite (i.e. high Ti, Al and Ba; low Cr), whereas other rims and intermediate zones (between cores and rims) exhibit unusually elevated Cr and lower Al and Ba concentrations. The latter compositions are indistinguishable from matrix phlogopite in polymict breccia xenoliths (considered to represent failed kimberlite intrusions) and from Ti-rich overgrowth rims on phlogopite in other mantle xenoliths. Consequently, it is likely that these phlogopite grains crystallized from kimberlite melts and that the high Ti-Cr zones originated from earlier kimberlite melts at mantle depths. We postulate that successive pulses of ascending kimberlite magma progressively metasomatised the conduit along which later kimberlite pulses ascended, producing progressively decreasing interaction with the surrounding mantle rocks. In our view, these processes represent the fundamental mechanism of kimberlite magma ascent. Our study also indicates that, in addition to xenoliths/xenocrysts and magmatic phases, kimberlite rocks incorporate material crystallized at various mantle depths by previous kimberlite intrusions (mantle-derived ‘antecrysts’).
Doklady Earth Sciences, Vol. 465, 1, pp. 1135-1138.
Russia
Deposit - Kimozero
Abstract: Geological and structural mapping of Paleoproterozoic Kimozero kimberlite with account for lithological facies and geochemical specialization provides evidence for the multiphase structure of the kimberlite pipe, which underwent fragmentation as a result of shear–faulting deformations. Two geochemical types of kimberlite (magnesium and carbonate) are distinguished.
In situ oxygen isotope, major-, and trace element constraints on the metasomatic modification and crustal origin of a Diamondiferous eclogite from Roberts Victor, Kaapvaal Craton.
Geochimica et Cosmochimica Acta, in press available, 45p.
Doklady Earth Sciences, Vol. 465, 1, pp. 1187-1190.
Russia
Deposit - Udachnaya
Abstract: The composition, structure, and morphology of iron-containing diamond-kimberlite contact sites were studied by means of scanning electron microscopy and Raman spectroscopy. The data obtained confirm the hypothesis of the similarity of mechanisms of diamond formation in nature and in experiments.
Abstract: The Mg isotopic compositions of garnet and clinopyroxene mineral separates and whole rocks from 21 xenolithic eclogites (11 low-MgO eclogites and 10 high-MgO eclogites) from the Koidu kimberlite complex, erupted within the Archean Man Shield, Sierra Leone, West Africa, provide new evidence bearing on the origin of cratonic eclogites. Garnet and clinopyroxene in both low-MgO and high-MgO eclogites generally record equilibrium inter-mineral Mg isotope partitioning, with ?26Mg varying from -2.15‰ to -0.46‰ in garnets and from -0.49‰ to +0.35‰ in clinopyroxenes. Bulk ?26Mg values (-1.38‰-to +0.05-), constructed from garnet and clinopyroxene data, are similar to results from rock powders (-1.60‰ to +0.17‰), suggesting that kimberlite infiltration has had negligible influence on the Mg isotopic compositions of the xenoliths. The ?26Mg values of low-MgO eclogites (-0.80‰ to +0.05‰) exceed the range of mantle peridotite xenoliths (-0.25- ± 0.04-), consistent with the eclogite’s derivation from recycled altered oceanic crust. Similarly variable ?26Mg values in high-MgO eclogites (-0.95‰ to -0.13‰), together with their high MgO and low FeO contents, suggest that high-MgO eclogites were produced by Mg-Fe exchange between partially molten low-MgO eclogites and surrounding peridotites. Our study shows that cratonic xenolithic eclogites preserve a record of Mg isotopic compositions produced by low-pressure, surficial isotope fractionations. The recycling of oceanic crust therefore increases the Mg isotope heterogeneity of the mantle.-
Canadian Journal of Earth Sciences, Vol. 52, pp. 1169-1181.
Canada, Ontario, Attawapiskat
Deposit - Victor
Abstract: The Moose River Basin in Ontario, Canada, contains nearly 1 km of Silurian marine strata, and although it has been studied for more than a century, its precise correlation globally has not been constrained. Herein, a core from the Victor Mine in the Moose River Basin was examined for conodont biostratigraphy and carbonate carbon (13Ccarb) isotope chemostratigraphy to provide a detailed chronostratigraphic framework for the Silurian strata (Severn River, Ekwan River, and Attawapiskat formations) in the Moose River Basin. The recovery of Aspelundia expansa, Aspelundia fluegeli fluegeli, Distomodus staurognathoides, Ozarkodina polinclinata estonica, Pterospathodus eopennatus, and Aulacognathus bullatus, as well as the lower Aeronian, upper Aeronian, lower Telychian (Valgu), and ascending limb of the Sheinwoodian (Ireviken) positive carbonate carbon (13Ccarb) isotope excursions provide significantly improved chronostratigraphic correlation of Llandovery strata in the Moose River Basin.
Earth and Planetary Science Letters, Vol. 435, 1, pp. 31-35.
Russia
Deposit - Udachnaya
Abstract: The study of diamond and its solid inclusions is of paramount importance to acquire direct information on the deepest regions of the Earth. However, although diamond is one of the most studied materials in geology, the diamond-inclusion relationships are not yet understood: do they form simultaneously (syngenesis) or are inclusions pre-existing objects on which diamond nucleated (protogenesis)? Here we report, for the first time, adhesion energies between diamond (D) and forsterite (Fo) to provide a crucial contribution to the syngenesis/protogenesis debate. The following interfaces were investigated at quantum-mechanical level: (i) (001)D/(001)Fo, (ii) (001)D/(021)Fo, and (iii) (111)D/(001)Fo. Our data, along with the ones recently obtained on the (110)D/(101)Fo interface, revealed an unexpected thermodynamic behaviour, all interfaces showing almost equal and low adhesion energies: accordingly, diamond and olivine have an extremely low chemical affinity and cannot develop preferential orientations, even during an eventual epitaxial growth. Combining these results with those of our previous work concerning the morphology constraints of diamond on its inclusions, we can state that the two main arguments used so far in favour of diamond/inclusions syngenesis cannot be longer considered valid, at least for olivine.
Doklady Earth Sciences, Vol. 465, 2, pp. 1297-1301.
Russia, Siberia
Deposit - Malokuonapskaya
Abstract: The U-Pb (SHRIMP) age was determined for zircons collected from 26 observation and sampling sites of diamonds and index minerals in the northeastern Siberian Platform. This part of the region hosts 15 low-diamondiferous Paleozoic and Mesozoic kimberlite fields, excluding the near economic Triassic Malokuonapskaya pipe in the Kuranakh field. Four epochs of kimberlite formation (Silurian, Late Devonian to Early Carboniferous, Middle to Late Triassic, and Middle to Late Jurassic) of the Siberian Platform, including its northeastern part, are confirmed as a result of our studies. Most observation points, including economic Quaternary diamond placers, contain Middle to Late Triassic zircons, which confirms the abundant Late Triassic volcanism in this region. The positive correlation of diamonds and major index minerals of kimberlites (mostly, garnets) at some observation sites indicates the possible Triassic age of the predictable diamondiferous kimberlites.
Abstract: The occurrence, morphology, and composition of rinkite are considered against the background of zoning in the Khibiny pluton. Accessory rinkite is mostly characteristic of foyaite in the outer part of pluton, occurs somewhat less frequently in foyaite and rischorrite in the central part of pluton, even more sparsely in foidolites and apatite-nepheline rocks, and sporadically in fenitized xenoliths of the Lovozero Formation. The largest, up to economic, accumulations of rinkite are related to the pegmatite and hydrothermal veins, which occur in nepheline syenite on both sides of the Main foidolite ring. The composition of rinkite varies throughout the pluton. The Ca, Na, and F contents in accessory rinkite and amorphous products of its alteration progressively increase from foyaite and fenitized basalt of the Lovozero Formation to foidolite, rischorrite, apatite-nepheline rocks, and pegmatite-hydrothermal veins.
Abstract: Xenoliths of mantle peridotite have been sampled from four kimberlite intrusions, Melton Wold, Hebron, Uintjiesberg and Markt, emplaced through the Mesoproterozoic Namaqua-Natal Belt, along the southern border of the Kaapvaal Craton. Although many of the xenoliths are heavily altered, constituent clinopyroxene, garnet and phlogopite are fresh and have been analysed by electron microprobe for major elements and by laser ablation ICP-MS for trace elements. Primitive mantle-normalised REE abundances in clinopyroxene are all strongly LREE enriched and show a range of patterns including uniformly MREE-HREE sloped (referred to here as ‘normal’), sinusoidal and humped sinusoidal patterns. HREE abundances are extremely low (Yb = 0.3-0.06 × PM). REEN patterns in coexisting garnets show a similar range of patterns. When normalised to primitive mantle values, trace element patterns in some clinopyroxenes show strong relative depletion in Rb-Ba, Ta-Nb and Ti, with some samples also being relatively depleted in Zr-Hf. These trace element characteristics are indistinguishable from those found in clinopyroxene and garnet from peridotites from the adjacent cratonic mantle. Numerical modelling of reactive porous flow of an enriched metasomatic melt through a geochemically depleted peridotite matrix can account for the full range in observed REEN patterns. The relative depletion in Rb-Ba, Ta-Nb and Ti can be accounted for by an early crystallisation of phlogopite from the percolating melt. The relative depletion in Zr-Hf in some clinopyroxenes requires either zircon to crystallise in the proximal metasomatic assemblage, or metasomatism by a carbonatitic melt. Modelling results, together with the absence of clinopyroxene with depleted or even partially enriched REEN patterns, suggest that all clinopyroxene has been modally introduced through metasomatism into an initially highly depleted harzburgitic protolith. The range in Sr and Pb isotopic composition of the clinopyroxenes indicates regional metasomatism by melts of various compositions. The strong HREEN depletion is interpreted to reflect the effect of initial melt depletion in the early Proterozoic, with melting extending into the spinel stability field requiring an oceanic realm, and again later in the Mesoproterozoic (Namaqua Orogeny). The superimposed incompatible element enrichment indicates subsequent multiple enrichment events by rising alkaline melts similar in composition to kimberlite or ultramafic alkaline lamprophyre, possibly related to Mesozoic plume upwelling beneath the region, that reintroduced clinopyroxene into the depleted Proterozoic harzburgite protolith.
Abstract: Zirconolite, its Ce-, Nd-, and Y-analogs, and laachite, another member of the zirconolite group, are typomorphic minerals of the fenitized xenoliths in nepheline syenite and foidolite of the Khibiny-Lovozero Complex, Kola Peninsula, Russia. All these minerals are formed at the late stage of fenitization as products of ilmentie alteration under the effect of Zr-bearing fluids. The diversity of these minerals is caused by the chemical substitutions of Na and Ca for REE, Th, and U compensated by substitution of Ti and Zr for Nb, Fe and Ta, as well as by the redistribution of REE between varieties enriched in Ti (HREE) or Nb (LREE). The results obtained can be used in the synthesis of Synroc-type titanate ceramics assigned for the immobilization of actinides.
Abstract: The Kovdor baddeleyite-apatite-magnetite deposit in the Kovdor phoscorite-carbonatite pipe is situated in the western part of the zoned alkali-ultrabasic Kovdor intrusion (NW part of the Fennoscandinavian shield; Murmansk Region, Russia). We describe major intrusive and metasomatic rocks of the pipe and its surroundings using a new classification of phoscorite-carbonatite series rocks, consistent with the IUGS recommendation. The gradual zonation of the pipe corresponds to the sequence of mineral crystallization (forsterite-hydroxylapatite-magnetite-calcite). Crystal morphology, grain size, characteristic inclusions, and composition of the rock-forming and accessory minerals display the same spatial zonation pattern, as do the three minerals of economic interest, i.e. magnetite, hydroxylapatite, and baddeleyite. The content of Sr, rare earth elements (REEs), and Ba in hydroxylapatite tends to increase gradually at the expense of Si, Fe, and Mg from early apatite-forsterite phoscorite (margins of the pipe) through carbonate-free, magnetite-rich phoscorite to carbonate-rich phoscorite and phoscorite-related carbonatite (inner part). Magnetite displays a trend of increasing V and Ca and decreasing Ti, Mn, Si, Cr, Sc, and Zn from the margins to the central part of the pipe; its grain size initially increases from the wall rocks to the inner part and then decreases towards the central part; characteristic inclusions in magnetite are geikielite within the marginal zone of the phoscorite-carbonatite pipe, spinel within the intermediate zone, and ilmenite within the inner zone. The zoning pattern seems to have formed due to both cooling and rapid degassing (pressure drop) of a fluid-rich magmatic column and subsequent pneumatolytic and hydrothermal processes.
Contributions to Mineralogy and Petrology, Vol. 171, 15p.
Canada, Northwest Territories
Deposit - Diavik
Abstract: Fibrous diamonds are often interpreted as direct precipitates of primary carbonate-bearing fluids in the lithospheric mantle, sourced directly from common reservoirs of “mantle” carbon and nitrogen. Here we have examined fibrous growth layers in five diamonds (as three rims or “coats” and two whole-crystal cuboids) from the Diavik Diamond Mine, Canada, using in situ C- and N-isotope and N-abundance measurements to investigate the origin and evolution of their parental fluids, and in particular, to test for isotopic variability within a suite of fibrous diamonds. High-resolution growth structure information was gleaned from cathodoluminescence (CL) imaging and, in combination with the isotopic data, was used to assess the nature of the transition from gem to fibrous growth in the coated diamonds. The two cuboids are characterized by fine concentric bands of fibrous and/or milky opaque diamond, with one sample (S1719) having intermittent gem-like growth layers that are transparent and colourless. The three coated diamonds comprise octahedral gem cores mantled by massive or weakly zoned fibrous rims, with sharp and well-defined gem-fibrous boundaries. For the two cuboid samples, ? 13C and ? 15N values were ?7.7 to ?3.2 ‰ (mean ?6.3 ± 1.3 ‰; 1 SD; n = 84) and ?5.6 to ?2.1 ‰ (mean ?4.0 ± 0.8 ‰; 1 SD; n = 48), respectively. The three fibrous rims have combined ? 13C values of ?8.3 to ?4.8 ‰ (mean ?6.9 ± 0.7 ‰; 1 SD; n = 113) and ? 15N values of ?3.8 to ?1.9 ‰ (mean ?2.7 ± 0.4 ‰; 1 SD; n = 43). N-abundances of the combined cuboid-fibrous rim dataset range from 339 to 1714 at. ppm. The gem cores have ? 13C and ? 15N values of ?5.4 to ?3.5 ‰ and ?17.7 to +4.5 ‰, respectively, and N-abundances of 480 to 1699 at. ppm. Broadly uniform C- and N-isotope compositions were observed in each of the gem cores (variations of ~<1 ‰ for carbon and ~<3 ‰ for nitrogen). This limited C- and N- isotope variability implies that the gem cores formed from separate pulses of fluid that remained isotopically uniform throughout the duration of growth. Significant isotopic and abundance differences were observed between the gem and fibrous growth zones, including in one detailed isotopic profile ? 13C and ? 15N offsets of ~?2.4 and ~?3.7 ‰, respectively, and a ~230 at. ppm increase in N-abundance. Combined with the well-defined gem-fibrous boundaries in plane light and CL, these sharp isotopic differences indicate separate parental fluid histories. Notably, in the combined fibrous diamond dataset prominent C- and N-isotope differences between the whole-crystal cuboid and fibrous rim data were observed, including a consistent ~1.3 ‰ offset in ? 15N values between the two growth types. This bimodal N-isotope distribution is interpreted as formation from separate parental fluids, associated with distinct nitrogen sources. The bimodal N-isotope distribution could also be explained by differences in N-speciation between the respective parental fluids, which would largely be controlled by the oxidation state of the fibrous rim and cuboid growth environments (i.e., N2 vs. NH4 + or NH3). We also note that this C- and N-isotope variability could indicate temporal changes to the source(s) of the respective parental fluids, such that each stage of fibrous diamond growth reflects the emplacement of separate pulses of proto-kimberlitic fluid—from distinct carbon and nitrogen sources, and/or with varying N-species—into the lithospheric mantle.
Russian Geology and Geophysics, Vol. 56, pp. 1717-1737.
Africa, Tanzania
Deposit - Oldoinyo Lengai
Abstract: The paper is concerned with study of melt inclusions in minerals of ijolite xenoliths at Oldoinyo Lengai Volcano. Melt inclusions with different phase compositions occur in forsterite macrocrysts and in diopside, nepheline, fluorapatite, Ti-andradite, and Ti-magnetite crystals. Nepheline contains primary melt inclusions (silicate glass + gas-carbonate globule ± submicron globules ± sulfide globule ± daughter/trapped phases, represented by diopside, fluorapatite, Ti-andradite, and alumoakermanite). The gas-carbonate globule consists of a gas bubble surrounded by a fine-grained aggregate of Na-Ca-carbonates (nyerereite and gregoryite). Fluorapatite contains primary carbonate-rich melt inclusions in the core, which consist of nyerereite, gregoryite, thenardite, witherite, fluorite, villiaumite, and other phases. Their mineral composition is similar to natrocarbonatites. Primary melt inclusions (glass + gas bubble ± daughter phases) are rare in diopside and Ti-andradite. Diopside and forsterite have trails of secondary carbonate-rich inclusions. Besides the above minerals, these inclusions contain halite, sylvite, neighborite, Na-Ca-phosphate, alkali sulfates, and other rare phases. In addition, diopside contains sulfide inclusions (pyrrhotite ± chalcopy- rite ± djerfisherite ± galena ± pentlandite). The chemical compositions of silicate glasses in the melt inclusions vary widely. The glasses are characterized by high Na, K, and Fe contents and low Al contents. They have high total alkali contents (16-23 wt.% Na2O + K2O) and peralkalinity index [(Na + K)/Al] ranging from 1.1 to 7.6. The carbonate-rich inclusions in the ijolite minerals are enriched in Na, P, S, and Cl. The data obtained indicate that the parental melt in the intermediate chamber was heterogeneous and contained silicate, natrocarbonate, and sulfide components during the ijolite crystallization. According to heating experiments with melt inclusions, silicate-carbonate liquid immiscibility occurred at temperature over 580 °C.
Russian Geology and Geophysics, Vol. 56, pp. 1701-1716.
Russia
Deposit - Grib
Abstract: New data on metasomatic processes in the lithospheric mantle in the central part of the Arkhangelsk diamondiferous province (ADP) are presented. We studied the major- and trace-element compositions of minerals of 26 garnet peridotite xenoliths from the V. Grib kimberlite pipe; 17 xenoliths contained phlogopite. Detailed mineralogical, petrographic, and geochemical studies of peridotite minerals (garnet, clinopyroxene, and phlogopite) have revealed two types of modal metasomatic enrichment of the lithospheric-mantle rocks: high temperature (melt) and low-temperature (phlogopite). Both types of modal metasomatism significantly changed the chemical composition of the peridotites. Low-temperature modal metasomatism manifests itself as coarse tabular and shapeless phlogopite grains. Two textural varieties of phlogopite show significant differences in chemical composition, primarily in the contents of TiO2, Cr2O3, FeO, Ba, Rb, and Cs. The rock-forming minerals of phlogopite-bearing peridotites differ in chemical composition from phlogopite-free peridotites, mainly in higher FeO content. Most garnets and clinopyroxenes in peridotites are the products of high-temperature mantle metasomatism, as indicated by the high contents of incompatible elements and REE pattern in these minerals. Fractional-crystallization modeling gives an insight into the nature of melts (metasomatic agents). They are close in composition to picrites of the Izhmozero field, basalts of the Tur’ino field, and carbonatites of the Mela field of the ADP. The REE patterns of the peridotite minerals make it possible to determine the sequence of metasomatic enrichment of the lithospheric mantle beneath the V. Grib kimberlite pipe.
Doklady Earth Sciences, Vol. 465, 2, pp. 1262-1267.
Russia
Deposit - Udachnaya
Abstract: Study of the mechanism of carbonation and wehrlitization of harzburgite upon metasomatism by carbonatitic melts of various genesis was carried out. Experiments with durations of 60-150 h were performed at 6.3 GPa and 1200°C. The data showed that carbonatite with MgO/CaO > 0.3 percolating into the peridotitic lithosphere may provide crystallization of magnesite in it. The influence of all studied carbonatites results in wehrlitization of peridotite. The compositions of melts formed by interaction with harzburgite (?2 wt % SiO2, Ca# = 36-47) practically do not depend on the composition of the initial carbonatite. Based on the data obtained, we conclude that the formation of magnesite-bearing and magnesite-free metasomatized peridotites may have a significant influence on the CO2 regime in the further generation of kimberlitic magmas of groups I and II.
Abstract: Coalingite, Mg10Fe2(CO3)(OH)24 • 2H2O, rare Mg -Fe hydrous carbonate, has been found in the course of the mineralogical study of a disintegrated kimberlite breccia from the Manchary pipe of the Khompu -May field located in the Tamma Basin, Central Yakutia, 100 km south of Yakutsk. Coalingite occurs as small reddish brown platelets, up to 0.2 mm in size. It is associated with lizardite, chrysotile and brucite, which are typical kimberlitic assemblage. Coalingite is a supergene mineral, but in this case, it is produced by the interaction of brucite-bearing kimberlite and underground water circulating through a vertical or oblique fault zone.
Geonomos *** IN POR, Vol. 19, 1, pp. 39-45. *** In Portuguese
South America, Brazil
Deposit - Coromandel area
Abstract: Hundreds of kimberlite intrusions and related rocks are known in the Coromandel region (MG), in the "Alto Paranaiba Diamondiferous Province", although the knowledge of these rocks is still scarce. Among these intrusions, it emphasizes the Grota do Cedro kimberlite, which outcrops in the drainage of same name at south of Coromandel (MG), hosted in micaschists of the Araxá Group (Neoproterozoic). The body has a roughly elliptical surface shape with 350 and 300 m axis; its chemical composition is similar to others of the province, and mineral chemistry of Cr-pyrope shows a strong concentration in the "G9" and "G5" fields. These chemical fields generally characterize diamond-poor or infertile intrusions.
Mineralogy and Petrology, in press available, 13p.
India
Deposit - Wajrakur
Abstract: Although Ti-rich garnets are commonly encountered in the groundmass of many alkaline igneous rocks, they are comparatively rare in kimberlites. Here we report on the occurrence of Ti-rich garnets in the groundmass of the P-15 and KL-3 kimberlites from the diamondiferous Wajrakarur field in the Eastern Dharwar craton of southern India. These garnets contain considerable Ti (11.7-23.9 wt.% TiO2), Ca (31.3-35.8 wt.% CaO), Fe (6.8-15.5 wt.% FeOT) and Cr (0.04-9.7 wt.% Cr2O3), but have low Al (0.2-5.7 wt.% Al2O3). In the case of the P-15 kimberlite they display a range in compositions from andradite to schorlomite, with a low proportion of grossular (andradite(17.7-49.9)schorlomite(34.6-49.5)-grossular(3.7-22.8)-pyrope(1.9-10.4)). A few grains also contain significant chromium and represent a solid solution between schorlomite and uvarovite. The Ti-rich garnets in the KL-3 kimberlite, in contrast, are mostly schorlomitic (54.9?90.9 mol %) in composition. The Ti-rich garnets in the groundmass of these two kimberlites are intimately associated with chromian spinels, perhaps suggesting that the garnet formed through the replacement of spinel. From the textural evidence, it appears unlikely that the garnets could have originated through secondary alteration, but rather seem to have formed through a process in which early magmatic spinels have reacted with late circulating, residual fluids in the final stages of crystallization of the kimberlite magma. Raman spectroscopy provides evidence for low crystallinity in the spinels which is likely to be a result of their partial transformation into andradite during their reaction with a late-stage magmatic (kimberlitic) fluid. The close chemical association of these Ti-rich garnets in TiO2-FeO-CaO space with those reported from ultramafic lamprophyres (UML) is also consistent with results predicted by experimental studies, and possibly implies a genetic link between kimberlite and UML magmas. The occurrence of Ti-rich garnets of similar composition in the Swartruggens orangeite on the Kaapvaal craton in South Africa, as well as in other kimberlites with an orangeitic affinity (e.g. the P-15 kimberlite on the Eastern Dharwar craton in southern India), is inferred to be a reflection of the high Ca- and high Ti-, and the low Al-nature, of the parent magma (i.e. Group II kimberlites).
Mineralogy and Petrology, in press available, 12p.
South America, Brazil
Deposit - Juina
Abstract: In addition to ultramafic and mafic associations, a primary natrocarbonatitic association occurs in the lower mantle. To date, it was identified as inclusions in diamonds from the Juina area, Mato Grosso State, Brazil. It comprises almost 50 mineral species: carbonates, halides, fluorides, phosphates, sulfates, oxides, silicates, sulfides and native elements. In addition, volatiles are present in this association. Among oxides, coexisting periclase and wüstite were identified, pointing to the formation of the natrocarbonatitic association at a depth greater than 2000 km. Some iron-rich (Mg,Fe)O inclusions in diamond are attributed to the lowermost mantle. The initial lower-mantle carbonatitic melt formed as a result of low-fraction partial melting of carbon-containing lower-mantle material, rich in P, F, Cl and other volatile elements, at the core-mantle boundary. During ascent to the surface, the initial carbonatitic melt dissociated into two immiscible parts, a carbonate-silicate and a chloride-carbonate melt. The latter melt is parental to the natrocarbonatitic lower-mantle association. Diamonds with carbonatitic inclusions were formed in carbonatitic melts or high-density fluids.
In situ oxygen-isotope, major, and trace element constraints on the metasomatic modification and crust origin of a Diamondiferous eclogite from Roberts Victor, Kaapvaal craton.
Geochimica et Cosmochimica Acta, Vol. 174, pp. 345-359.
Contributions to Mineralogy and Petrology, Vol. 171, 11, 24p.
Africa, South Africa
Deposit - Bellsbank
Abstract: An oceanic crustal origin is the commonly accepted paradigm for mantle-derived eclogites. However, the significance of the aluminous members of the eclogite suite, containing kyanite and corundum, has long been underrated and their role neglected in genetic models of cratonic evolution. Here, we present a geochemical and petrological study of a suite of kyanite- and corundum-bearing eclogites from the Bellsbank kimberlite, S. Africa, which originate from depths between 150 and 200 km. Although clearly of high-pressure provenance, these rocks had a low-pressure cumulative origin with plagioclase and olivine as major cumulate phases. This is shown by the very pronounced positive Eu anomalies, low REE abundances, and ? 18O values lower than the Earth’s mantle. Many chemical features are identical to modern-day troctolitic cumulates including a light REE depletion akin to MORB, but there are also distinguishing features in that the eclogites are richer in Na, Fe, and Ni. Two of the eclogites have a minimum age of ~3.2 Ga, defined by the extremely unradiogenic 87Sr/86Sr (0.7007) in clinopyroxene. Phase equilibria indicate that the parent melts were formed by partial melting below an Archean volcanic center that generated (alkali-)picritic to high-alumina tholeiitic melts from a mantle whose oxygen fugacity was lower than today. Fractional crystallization produced troctolites with immiscible sulfide melt droplets within the mafic crust. Instability of the mafic crust led to deep subduction and re-equilibration at 4 6 GPa. Phase relationships plus the presence of a sample with appreciable modal corundum but no Eu anomaly suggest that kyanite- and corundum-bearing eclogites may also originate as plagioclase-free, higher pressure cumulates of highly aluminous clinopyroxene, spinel, and olivine. This is consistent with the crystallizing phase assemblage from an olivine tholeiitic to picritic magma deeper in the Archean oceanic crust or uppermost mantle. We postulate that the magmatic and subduction processes driving modern plate tectonics already existed in the Meso- to Early Archean.
Physics and Chemistry of Minerals, Vol. 42, 9, pp. 707-722.
South America, Brazil
Deposit - Sao-Luis
Abstract: Photoluminescence (PL) spectroscopy and electron paramagnetic resonance (EPR) were used for the first time to characterize properties of superdeep diamonds from the São-Luis alluvial deposits (Brazil). The infrared measurements showed the low nitrogen content (>50 of 87 diamonds from this locality were nitrogen free and belonged to type IIa) and simultaneously the extremely high level of nitrogen aggregation (pure type IaB being predominant), which indicates that diamonds under study might have formed under high pressure and temperature conditions. In most cases, PL features excited at various wavelengths (313, 473, and 532 nm) were indicative of different growth and post-growth processes during which PL centers could be formed via interaction between vacancies and nitrogen atoms. The overall presence of the 490.7 nm, H3, and H4 centers in the luminescence spectra attests to strong plastic deformations in these diamonds. The neutral vacancy known as the GR1 center has probably occurred in a number of crystals due to radiation damage in the post-growth period. The 558.5 nm PL center is found to be one of the most common defects in type IIa samples which is accompanied by the EPR center with g-factor of 2.00285. The 536 and 576 nm vibronic systems totally dominated the PL spectra of superdeep diamonds, while none of “normal” diamonds from the Mir pipe (Yakutia) with similar nitrogen characteristics showed the latter three PL centers.
Abstract: In recent years, several studies have focused on the growth conditions of the diamonds through the analysis of the mineral inclusions trapped in them. In these studies, it is crucial to distinguish between protogenetic, syngenetic and epigenetic inclusions. X-ray topography (XRDT) can be a helpful tool to verify, in a non-destructive way, the genetic nature of inclusions in diamond. With this aim, a diamond from the Udachnaya kimberlite, Siberia, was investigated. The diamond, previously studied by Nestola et al. (2011), has anomalous birefringence and the two largest olivines have typical “diamond-imposed” shapes. The study of the topographic images shows that the diamond exhibits significant deformation fields related to post growth plastic deformation. The absence of dislocations starting from the olivine inclusions, and the dark contrasts around them represent the main results obtained by XRDT, contributing to the elucidation of the relationships between the diamond and the olivines at the micron-meter scale. The dark halo surrounding the inclusions was likely caused by the effect of different thermo-elastic properties between the diamond and the inclusions. The absence of dislocations indicates that the diamond-imposed morphology did not produce the volume distortion commonly associated with the entrapment of the full-grown inclusions and, thus, only based on such evidence, a syngenetic origin could be proposed. In addition, stepped figures optically observed at the interface between diamond and one of the olivines suggest processes of selective partial dissolution that would contribute to a change in the final morphology of inclusions. These results show that a diamond morphology may be imposed to a full-grown (protogenetic) olivine during their encapsulation, suggesting that the bulk of the inclusion is protogenetic, whereas its more external regions, close to the diamond-inclusion interface, could be syngenetic.
Geochimica et Cosmochimica Acta, Vol. 179, pp. 156-176.
Africa, South Africa
Deposit - Lace
Abstract: Diamond- and kyanite-bearing eclogites from the Lace kimberlite on the Kaapvaal craton have common picritic to gabbroic oceanic protoliths with bimineralic eclogites, lying on arrays of Eu? and ?REE that are consistent with accumulation and fractionation of plagioclase and olivine. However, they also show significant compositional differences, such as more grossular-rich garnet and aluminous clinopyroxene (cpx), which require the operation of additional processes. Their nature is elucidated using mineral major- and trace-element compositions, as well as Sr isotope ratios determined by in situ techniques.Highly variable major-element compositions across the co-genetic eclogite suites exert a strong effect on the trace-element distribution between garnet and cpx, whereby Sc, Ge, Sr, Y, Cd, REE, Th and U partition more strongly into garnet with increasing grossular-content. Thus, significant differences between the trace-element compositions of garnet can ensue from crystal-chemical effects alone, making their use as petrogenetic indicators potentially ambiguous. After correcting for these compositional effects, garnet in kyanite-/diamond eclogites, and in eclogites devoid of accessory minerals but with similar signatures, shows depletion (or dilution) in Sc, Ge, Y, In, Zr, Hf and the HREE, and enrichment in the LREE and Th compared to garnet in bimineralic eclogites. This is interpreted as the signature of a pelite-derived melt, which was transferred by addition of aluminous cpx that later exsolved kyanite and garnet, as observed in other aluminous eclogite suites. Continental input can explain initial (at 2.9 Ga) 87Sr/86Sr ? 0.714 measured in cpx in eleven samples with low 87Rb/86Sr (<0.01). The association of diamond with kyanite suggests that diamond formation is also linked to this event, possibly due to diamond formation by oxidation of reduced carbon, such as methane, and attendant reduction of Fe3+ in garnet. This model of sediment melt-oceanic crust interaction reconciles evidence for both low- and high-pressure igneous processes in some aluminous eclogites. We suggest that a subduction mélange is a favourable setting for the transfer of a sediment-derived signature into oceanic crust, leading to formation of diamondiferous kyanite-eclogites from bimineralic eclogites. Diapirism, fluxed by the presence of partial melt, may have facilitated dispersal of the eclogites in the lithosphere column, consistent with their widely varying equilibration pressures ranging from ?5 to 8 GPa.
Bussweiler, Y., Pearson, D.G., Luth, R.W., Kjarsgaard, B.A., Stachel, T.
The evolution of calcite-bearing kimberlite by rock-melt reaction during ascent - evidence from polymineralic inclusions within Cr- diopside and Cr-pyrope megacrysts from Lac de Gras kimberlites, Northwest Territories, Canada.
GAC MAC Meeting Special Session SS11: Cratons, kimberlites and diamonds., abstract 1/4p.
Mineralogy and Petrology, in press available, 25p.
India
Deposit - Sakri Nuapada
Abstract: We report the mineralogy, bulk-rock geochemistry, 40Ar/39Ar (whole-rock) age and radiogenic (Sr and Nd) isotope composition of an ultrapotassic dyke from Sakri (Nuapada lamproite field) located at the tectonic contact between the easternmost margin of the Bastar craton and Eastern Ghats Mobile Belt, India. The Sakri dyke has a mineralogy which strongly resembles a lamproite sensu stricto (viz.,Ti-rich phlogopite, Na-poor diopside, Fe-rich sanidine, ulvospinel trend and Sr-rich apatite). However, its bulk-rock major element geochemical characteristics (viz., extreme silica-undersaturated nature) resemble sensu lato kamafugite from Toro Ankole, Uganda, East African Rift, and Alto Paranaiba Province, Brazil. The Sakri dyke also displays certain compositional peculiarities (viz., high degree of evolution of mica composition from phlogopite to biotite, elevated titanium and aluminum in clinopyroxene and significantly lower bulk Mg#) when compared to the ultrapotassic rocks from various Indian cratons. 40Ar/39Ar dating gave a plateau age of 1045?±?9 Ma which is broadly similar to that of other Mesoproterozoic (i) lamproites from the Bastar and Bundelkhand cratons, and (ii) kimberlites from the Eastern Dharwar craton. Initial bulk-rock Sr (0.705865-0.709024) and Nd (0.511063-0.511154) isotopic ratios reveal involvement of an ‘enriched’ source region with long-term incompatible element enrichment and a depleted mantle (TDM) Nd model age of 2.56 Ga straddling the Archaean-Proterozoic chronostratigraphic boundary. The bulk-rock incompatible trace element ratios (Ta/Yb, Th/Yb, Rb/Ba and Ce/Y) of the Sakri ultrapotassic dyke negate any significant influence of crustal contamination. Small-degree melting (1 to 1.5 %) of a mixed garnet-facies and spinel-facies phlogopite lherzolite can account for its observed REE concentrations. Whereas the emplacement of the Sakri ultrapotassic dyke is related to the amalgamation of the supercontinent of Rodinia, its overlapping geochemical characteristics of lamproite and kamafugite (also displayed by two other lamproites of the Nuapada field at Amlidadar and Parkom) are linked to the emplacement in a unique geological setting at the craton-mobile belt contact and hence of geodynamic significance.
Abstract: The comprehensive petrographical, petrochemical and mineralogical study of the Kovdor magnetite-apatite-baddeleyite deposit in the phoscorite-carbonatite complex (Murmansk Region, Russia) revealed a spatial distribution of grain size and chemical composition of three economically extractable minerals — magnetite, apatite, and baddeleyite, showing that zonal distribution of mineral properties mimics both concentric and vertical zonation of the carbonatite-phoscorite pipe. The marginal zone of the pipe consists of (apatite)-forsterite phoscorite carrying fine grains of Ti-Mn-Si-rich magnetite with ilmenite exsolution lamellae, fine grains of Fe-Mg-rich apatite and finest grains of baddeleyite, enriched in Mg, Fe, Si and Mn. The intermediate zone accommodates carbonate-free magnetite-rich phoscorites that carry medium to coarse grains of Mg-Al-rich magnetite with exsolution inclusions of spinel, medium-grained pure apatite and baddeleyite. The axial zone hosts carbonate-rich phoscorites and phoscorite-related carbonatites bearing medium-grained Ti-V-Ca-rich magnetite with exsolution inclusions of geikielite-ilmenite, fine grains of Ba-Sr-Ln-rich apatite and comparatively large grains of baddeleyite, enriched in Hf, Ta, Nb and Sc. The collected data enable us to predict such important mineralogical characteristics of the multicomponent ore as chemical composition and grain size of economic and associated minerals, presence of contaminating inclusions, etc. We have identified potential areas of maximum concentration of such by-products as scandium, niobium and hafnium in baddeleyite and REEs in apatite.
Abstract: Experiments on the origin of the Udachnaya-East kimberlite (UEK) have been performed using a Kawai-type multianvil apparatus at 3-6.5GPa and 900-1500°C. The studied composition represents exceptionally fresh Group-I kimberlite containing (wt.%): SiO2=25.9, TiO2=1.8, Al2O3=2.8, FeO=9.0, MgO=30.1, CaO=12.7, Na2O=3.4, K2O=1.3, P2O5=1.0, Cl=0.9, CO2=9.9, and H2O=0.5. The super-solidus assemblage consists of melt, olivine (Ol), Ca-rich (26.0-30.2wt.% CaO) garnet (Gt), Al-spinel (Sp), perovskite (Pv), a CaCO3 phase (calcite or aragonite), and apatite. The low pressure assemblage (3-4GPa) also includes clinopyroxene. The apparent solidus was established between 900 and 1000°C at 6.5GPa. At 6.5GPa and 900°C Na-Ca carbonate with molar ratio of (Na+K)/Ca?0.44 was observed. The UEK did not achieve complete melting even at 1500°C and 6.5GPa, due to excess xenogenic Ol in the starting material. In the studied P-T range, the melt has a Ca-carbonatite composition (Ca#=molar Ca/(Ca+Mg) ratio=0.62-0.84) with high alkali and Cl contents (7.3-11.4wt.% Na2O, 2.8-6.7wt.% K2O, 1.6-3.4wt.% Cl). The K, Na and Cl contents and Ca# decrease with temperature. It is argued that the primary kimberlite melt at depths>200km was an essentially carbonatitic (<5wt.% SiO2), but evolved toward a carbonate-silicate composition (up to 15-20wt.% SiO2) during ascent. The absence of orthopyroxene among the run products indicates that xenogenic orthopyroxene was preferentially dissolved into the kimberlite melt. The obtained subliquidus phase assemblage (Ol+Sp+Pv+Ca-rich Gt) at P-T conditions of the UEK source region, i.e. where melt was in the last equilibrium with source rock before magma ascent, differs from the Opx-bearing peridotitic mineral assemblage of the UEK source region. This difference can be ascribed to the loss of substantial amounts of CO2 from the kimberlite magma at shallow depths, as indicated by both petrological and experimental data. Our study implies that alkali-carbonatite melt would be a liquid phase within mantle plumes generated at the core-mantle boundary or shallower levels of the mantle, enhancing the ascent velocity of the plumes. We conclude that the long-term activity of a rising hot mantle plume and associated carbonatite melt (i.e. kimberlite melt) causes thermo-mechanical erosion of the subcontinental lithosphere mantle (SCLM) roots and creates hot and deformed metasomatic regions in the lower parts of the SCLM, which corresponds to depths constrained by P-T estimates of sheared Gt-peridotite xenoliths. The sheared Gt-peridotites undoubtedly represent samples of these regions.
Abstract: Perovskite (CaTiO3) has become a very usefulmineral for dating kimberlite eruptions, aswell as for constraining the compositional evolution of a kimberlitic magma and its source. Despite the undeniable potential of such an approach, no similar study had been done in Angola, the fourth largest diamond producer in Africa. Here we present the firstwork of in situ U-Pb geochronology and Sr-Ndisotope analyses of perovskite in six Angolan kimberlites, supported by a detailed petrographic and geochemical study of their perovskite populations. Four types of perovskitewere identified, differing in texture,major- and trace-element composition, zoning patterns, type of alteration and the presence or absence of inclusions. Primary groundmass perovskite is classified either as anhedral, Na-, Nb- and LREE-poor perovskite (Ia); or euhedral, strongly zoned, Na-, Nb- and LREE-rich perovskite (Ib). Secondary perovskite occurs as reaction rims on ilmenite (IIa) or as high Nb (up to 10.6 wt% Nb2O5) perovskite rims on primary perovskite (IIb). The occurrence of these four types within the Mulepe kimberlites is interpreted as an evidence of a complex, multi-stage process that involved mingling of compositionally different melts. U-Pb dating of these perovskites yielded Lower Cretaceous ages for four of the studied kimberlites: Mulepe 1 (116.2±6.5Ma),Mulepe 2 (123.0±3.6Ma), Calonda (119.5±4.3 Ma) and Cat115 (133±10Ma). Kimberlite magmatism occurred in NE Angola likely due to reactivation of deep-seated translithospheric faults (N300 km) during the break-up of Gondwana. Sr-Nd isotope analyses of four of these kimberlites indicate that they are Group I kimberlites, which is consistent with the petrological observations.
Mineralogy and Petrology, Vol. 110, 2, pp. 295-307.
India
Deposit - Wajrakarur
Abstract: Although Ti-rich garnets are commonly encountered in the groundmass of many alkaline igneous rocks, they are comparatively rare in kimberlites. Here we report on the occurrence of Ti-rich garnets in the groundmass of the P-15 and KL-3 kimberlites from the diamondiferous Wajrakarur field in the Eastern Dharwar craton of southern India. These garnets contain considerable Ti (11.7-23.9 wt.% TiO2), Ca (31.3-35.8 wt.% CaO), Fe (6.8-15.5 wt.% FeOT) and Cr (0.04-9.7 wt.% Cr2O3), but have low Al (0.2-5.7 wt.% Al2O3). In the case of the P-15 kimberlite they display a range in compositions from andradite to schorlomite, with a low proportion of grossular (andradite(17.7-49.9)schorlomite(34.6-49.5)-grossular(3.7-22.8)-pyrope(1.9-10.4)). A few grains also contain significant chromium and represent a solid solution between schorlomite and uvarovite. The Ti-rich garnets in the KL-3 kimberlite, in contrast, are mostly schorlomitic (54.9?90.9 mol %) in composition. The Ti-rich garnets in the groundmass of these two kimberlites are intimately associated with chromian spinels, perhaps suggesting that the garnet formed through the replacement of spinel. From the textural evidence, it appears unlikely that the garnets could have originated through secondary alteration, but rather seem to have formed through a process in which early magmatic spinels have reacted with late circulating, residual fluids in the final stages of crystallization of the kimberlite magma. Raman spectroscopy provides evidence for low crystallinity in the spinels which is likely to be a result of their partial transformation into andradite during their reaction with a late-stage magmatic (kimberlitic) fluid. The close chemical association of these Ti-rich garnets in TiO2-FeO-CaO space with those reported from ultramafic lamprophyres (UML) is also consistent with results predicted by experimental studies, and possibly implies a genetic link between kimberlite and UML magmas. The occurrence of Ti-rich garnets of similar composition in the Swartruggens orangeite on the Kaapvaal craton in South Africa, as well as in other kimberlites with an orangeitic affinity (e.g. the P-15 kimberlite on the Eastern Dharwar craton in southern India), is inferred to be a reflection of the high Ca- and high Ti-, and the low Al-nature, of the parent magma (i.e. Group II kimberlites).
Abstract: The comprehensive petrographical, petrochemical and mineralogical study of the Kovdor magnetite-apatite-baddeleyite deposit in the phoscorite-carbonatite complex (Murmansk Region, Russia) revealed a spatial distribution of grain size and chemical composition of three economically extractable minerals — magnetite, apatite, and baddeleyite, showing that zonal distribution of mineral properties mimics both concentric and vertical zonation of the carbonatite-phoscorite pipe. The marginal zone of the pipe consists of (apatite)-forsterite phoscorite carrying fine grains of Ti-Mn-Si-rich magnetite with ilmenite exsolution lamellae, fine grains of Fe-Mg-rich apatite and finest grains of baddeleyite, enriched in Mg, Fe, Si and Mn. The intermediate zone accommodates carbonate-free magnetite-rich phoscorites that carry medium to coarse grains of Mg-Al-rich magnetite with exsolution inclusions of spinel, medium-grained pure apatite and baddeleyite. The axial zone hosts carbonate-rich phoscorites and phoscorite-related carbonatites bearing medium-grained Ti-V-Ca-rich magnetite with exsolution inclusions of geikielite-ilmenite, fine grains of Ba-Sr-Ln-rich apatite and comparatively large grains of baddeleyite, enriched in Hf, Ta, Nb and Sc. The collected data enable us to predict such important mineralogical characteristics of the multicomponent ore as chemical composition and grain size of economic and associated minerals, presence of contaminating inclusions, etc. We have identified potential areas of maximum concentration of such by-products as scandium, niobium and hafnium in baddeleyite and REEs in apatite.
Deposit - Bayan Obo, Mountain Pass, Motzfeldt, Ilimaussaq
Abstract: Rare earth elements (REEs) generate characteristic absorption features in visible to shortwave infrared (VNIR-SWIR) reflectance spectra. Neodymium (Nd) has among the most prominent absorption features of the REEs and thus represents a key pathfinder element for the REEs as a whole. Given that the world’s largest REE deposits are associated with carbonatites, we present spectral, petrographic, and geochemical data from a predominantly carbonatitic suite of rocks that we use to assess the feasibility of imaging REE deposits using remote sensing. Samples were selected to cover a wide range of extents and styles of REE mineralization, and encompass calcio-, ferro- and magnesio-carbonatites. REE ores from the Bayan Obo (China) and Mountain Pass (United States) mines, as well as REE-rich alkaline rocks from the Motzfeldt and Ilímaussaq intrusions in Greenland, were also included in the sample suite. The depth and area of Nd absorption features in spectra collected under laboratory conditions correlate positively with the Nd content of whole-rock samples. The wavelength of Nd absorption features is predominantly independent of sample lithology and mineralogy. Correlations are most reliable for the two absorption features centered at ~744 and ~802 nm that can be observed in samples containing as little as ~1,000 ppm Nd. By convolving laboratory spectra to the spectral response functions of a variety of remote sensing instruments we demonstrate that hyperspectral instruments with capabilities equivalent to the operational Airborne Visible-Infrared Imaging Spectrometer (AVIRIS) and planned Environmental Mapping and Analysis Program (EnMAP) systems have the spectral resolutions necessary to detect Nd absorption features, especially in high-grade samples with economically relevant REE accumulations (Nd > 30,000 ppm). Adding synthetic noise to convolved spectra indicates that correlations between Nd absorption area and whole-rock Nd content only remain robust when spectra have signal-to-noise ratios in excess of ~250:1. Although atmospheric interferences are modest across the wavelength intervals relevant for Nd detection, most REE-rich outcrops are too small to be detectable using satellite-based platforms with >30-m spatial resolutions. However, our results indicate that Nd absorption features should be identifiable in high-quality, airborne, hyperspectral datasets collected at meter-scale spatial resolutions. Future deployment of hyperspectral instruments on unmanned aerial vehicles could enable REE grade to be mapped at the centimeter scale across whole deposits.
Deposit - Bayan Obo, Mountain Pass, Motzfeldt, Ilimaussaq
Abstract: Rare earth elements (REEs) generate characteristic absorption features in visible to shortwave infrared (VNIR-SWIR) reflectance spectra. Neodymium (Nd) has among the most prominent absorption features of the REEs and thus represents a key pathfinder element for the REEs as a whole. Given that the world’s largest REE deposits are associated with carbonatites, we present spectral, petrographic, and geochemical data from a predominantly carbonatitic suite of rocks that we use to assess the feasibility of imaging REE deposits using remote sensing. Samples were selected to cover a wide range of extents and styles of REE mineralization, and encompass calcio-, ferro- and magnesio-carbonatites. REE ores from the Bayan Obo (China) and Mountain Pass (United States) mines, as well as REE-rich alkaline rocks from the Motzfeldt and Ilímaussaq intrusions in Greenland, were also included in the sample suite. The depth and area of Nd absorption features in spectra collected under laboratory conditions correlate positively with the Nd content of whole-rock samples. The wavelength of Nd absorption features is predominantly independent of sample lithology and mineralogy. Correlations are most reliable for the two absorption features centered at ~744 and ~802 nm that can be observed in samples containing as little as ~1,000 ppm Nd. By convolving laboratory spectra to the spectral response functions of a variety of remote sensing instruments we demonstrate that hyperspectral instruments with capabilities equivalent to the operational Airborne Visible-Infrared Imaging Spectrometer (AVIRIS) and planned Environmental Mapping and Analysis Program (EnMAP) systems have the spectral resolutions necessary to detect Nd absorption features, especially in high-grade samples with economically relevant REE accumulations (Nd > 30,000 ppm). Adding synthetic noise to convolved spectra indicates that correlations between Nd absorption area and whole-rock Nd content only remain robust when spectra have signal-to-noise ratios in excess of ~250:1. Although atmospheric interferences are modest across the wavelength intervals relevant for Nd detection, most REE-rich outcrops are too small to be detectable using satellite-based platforms with >30-m spatial resolutions. However, our results indicate that Nd absorption features should be identifiable in high-quality, airborne, hyperspectral datasets collected at meter-scale spatial resolutions. Future deployment of hyperspectral instruments on unmanned aerial vehicles could enable REE grade to be mapped at the centimeter scale across whole deposits.
Doklady Earth Sciences, Vol. 466, 2, Feb. pp. 173-176.
Russia, Yakutia
Deposit - International
Abstract: The results of study of rutile inclusions in pyrope from the Internatsionalnaya kimberlite pipe are presented. Rutile is characterized by unusually high contents of impurities (up to 25 wt %). The presence of Cr2O3 (up to 9.75 wt %) and Nb2O5 (up to 15.57 wt %) are most typical. Rutile inclusions often occur in assemblage with Ti-rich oxides: picroilmenite and crichtonite group minerals. The Cr-pyropes with inclusions of rutile, picroilmenite, and crichtonite group minerals were formed in the lithospheric mantle beneath the Mirnyi field during their joint crystallization from melts enriched in Fe, Ti, and other incompatible elements as a result of metasomatic enrichment of the depleted lithospheric mantle.
Abstract: The results of the first study of the PGE distribution in deformed lherzolites of the Udachnaya kimberlite pipe (Yakutia) are presented here. The complex character of evolution of the PGE composition in the Deformed lherzolites is assumed to be the result of silicate metasomatism. At the first stage, growth in the amount of clinopyroxene and garnet in the rock is accompanied by a decrease in the concentration of the compatible PGE (Os, Ir). During the final stage, the rock is enriched with incompatible PGE (Pt, Pd) and Re possible due to precipitation of submicron-sized particles of sulfides in the interstitial space of these mantle rocks.
Abstract: Paragenetic analysis of pyropes from alluvial deposits of the Muna—Markha interfluve (Sakha-Yakutia Republic) made it possible to distinguish relatively uniform areas that are promising for the discovery of kimberlite bodies.
Abstract: Tychite Na6Mg2(CO3)4(SO3) is a rare natural Na and Mg sulfatocarbonate. It is found only as minor mineral in deposits of saline lakes in the United States, Canada, Uganda, and China. In these continental evaporites tychite has sedimentary genesis. In this study, we report the first occurrence of tychite as a crystal phase in the melt inclusions in olivine from mantle xenoliths of the Udachnaya-East kimberlite pipe. This find provides an evidence for the probability of tychite crystallization from melts; i.e., this rare sulfatocarbonate may have a magmatic origin as well.
Abstract: The lack of consensus on the possible range of initial kimberlite melt compositions and their evolution as they ascend through and interact with mantle and crustal wall rocks, hampers a complete understanding of kimberlite petrogenesis. Attempts to resolve these issues are complicated by the fact that kimberlite rocks are mixtures of magmatic, xenocrystic and antecrystic components and, hence, are not directly representative of their parental melt composition. Furthermore, there is a lack of direct evidence of the assimilation processes that may characterise kimberlitic melts during ascent, which makes understanding their melt evolution difficult. In this contribution we provide novel constraints on the interaction between precursor kimberlite melts and lithospheric mantle wall rocks. We present detailed textural and geochemical data for a carbonate-rich vein assemblage that traverses a garnet wehrlite xenolith [equilibrated at ~ 1060 °C and 43 kbar (~ 140-145 km)] from the Bultfontein kimberlite (Kimberley, South Africa). This vein assemblage is dominated by Ca-Mg carbonates, with subordinate oxide minerals, olivine, sulphides, and apatite. Vein phases have highly variable compositions indicating formation under disequilibrium conditions. Primary inclusions in the vein minerals and secondary inclusion trails in host wehrlite minerals contain abundant alkali-bearing phases (e.g., Na-K bearing carbonates, Mg-freudenbergite, Na-bearing apatite and phlogopite). The Sr-isotope composition of vein carbonates overlaps those of groundmass calcite from the Bultfontein kimberlite, as well as perovskite from the other kimberlites in the Kimberley area. Clinopyroxene and garnet in the host wehrlite are resorbed and have Si-rich reaction mantles where in contact with the carbonate-rich veins. Within some veins, the carbonates occur as droplet-like, globular segregations, separated from a similarly shaped Si-rich phase by a thin meniscus of Mg-magnetite. These textures are interpreted to represent immiscibility between carbonate and silicate melts. The preservation of reaction mantles, immiscibility textures and disequilibrium in the vein assemblage, suggests quenching, probably triggered by entrainment and rapid transport toward the Earth's surface in the host kimberlite magma. Based on the Sr-isotope systematics of vein carbonate minerals, and the close temporal relationship between carbonate-rich metasomatism and kimberlite magmatism, we suggest that the carbonate-rich vein assemblage was produced by the interaction between a melt genetically related to the Bultfontein kimberlite and wehrlitic mantle wall rock. If correct, this unique xenolith sample provides a rare snapshot of the assimilation processes that might characterise parental kimberlite melts during their ascent through the lithospheric mantle.
Contributions to Mineralogy and Petrology, Vol. 171, 7, 25p.
Canada, Northwest Territories
Deposit - Lac de Gras arena
Abstract: Megacrystic (>1 cm) clinopyroxene (Cr-diopside) and garnet (Cr-pyrope) xenocrysts within kimberlites from Lac de Gras (Northwest Territories, Canada) contain fully crystallized melt inclusions. These ‘polymineralic inclusions’ have previously been interpreted to form by necking down of melts at mantle depths. We present a detailed petrographical and geochemical investigation of polymineralic inclusions and their host crystals to better understand how they form and what they reveal about the evolution of kimberlite melt. Genetically, the megacrysts are mantle xenocrysts with peridotitic chemical signatures indicating an origin within the lithospheric mantle (for the Cr-diopsides studied here ~4.6 GPa, 1015 °C). Textural evidence for disequilibrium between the host crystals and their polymineralic inclusions (spongy rims in Cr-diopside, kelyphite in Cr-pyrope) is consistent with measured Sr isotopic disequilibrium. The preservation of disequilibrium establishes a temporal link to kimberlite eruption. In Cr-diopsides, polymineralic inclusions contain phlogopite, olivine, chromite, serpentine, and calcite. Abundant fluid inclusion trails surround the inclusions. In Cr-pyropes, the inclusions additionally contain Al-spinel, clinopyroxene, and dolomite. The major and trace element compositions of the inclusion phases are generally consistent with the early stages of kimberlite differentiation trends. Extensive chemical exchange between the host phases and the inclusions is indicated by enrichment of the inclusions in major components of the host crystals, such as Cr2O3 and Al2O3. This chemical evidence, along with phase equilibria constraints, supports the proposal that the inclusions within Cr-diopside record the decarbonation reaction: dolomitic melt + diopside ? forsterite + calcite + CO2, yielding the observed inclusion mineralogy and producing associated (CO2-rich) fluid inclusions. Our study of polymineralic inclusions in megacrysts provides clear mineralogical and chemical evidence for an origin of kimberlite that involves the reaction of high-pressure dolomitic melt with diopside-bearing mantle assemblages producing a lower-pressure melt that crystallizes a calcite-dominated assemblage in the crust.
European Journal of Mineralogy, Vol. 28, pp. 329-336.
Russia
Deposit - Udachnaya
Abstract: An experimental simulation of serpentine and chromite interaction was conducted at the pressure (P) and temperature (T) conditions of garnet-peridotite stability in order to clarify the potential role of serpentinite as a source for the crystallization of subcalcic garnet in the depleted subcratonic mantle. The experiments were performed at 4 GPa and 1100 C and 5.5 GPa and 1200 C using the high-pressure apparatus BARS. Natural antigorite from ophiolites of the Eastern Sayan (Russia) was used as a starting material. Two groups of chromite grains with different Cr# ¼ 100Cr/(Cr þ Al) ratios (from spinel peridotite xenoliths from the Udachnaya kimberlite pipe, Yakutia) were added to the antigorite. Newly formed garnet, spinel, olivine and orthopyroxene were observed as the products in the experiments. Garnet formed only around chromite grains with the lower Cr# value (46.4). Garnet has low CaO contents (,0.05 -1.10 wt.%) with chromium contents showing wide intra- and inter-grain variations (Cr# ¼ 0.7 -33.5). The Cr content increases from core to rim with the outer zones corresponding most closely to the equilibrium composition of the relevant bulk composition. The garnet total FeO content is in the range 3.4 -5.8 wt.%. The experiments demonstrate that serpentinite decomposed at a temperature of 700 C to olivine þ orthopyroxene þ water. If mingled mechanically with spinel-bearing mantlewedge peridotite upon subduction, it could react to form the range of subcalcic garnet compositions found as inclusions in diamonds.
Abstract: Diamonds and their inclusions are unique probes into the deep Earth, tracking the deep carbon cycle to >800?km. Understanding the mechanisms of carbon mobilization and freezing is a prerequisite for quantifying the fluxes of carbon in the deep Earth. Here we show direct evidence for the formation of diamond by redox reactions involving FeNi sulfides. Transmission Kikuchi Diffraction identifies an arrested redox reaction from pyrrhotite to magnetite included in diamond. The magnetite corona shows coherent epitaxy with relict pyrrhotite and diamond, indicating that diamond nucleated on magnetite. Furthermore, structures inherited from h-Fe3O4 define a phase transformation at depths of 320 -330?km, the base of the Kaapvaal lithosphere. The oxidation of pyrrhotite to magnetite is an important trigger of diamond precipitation in the upper mantle, explaining the presence of these phases in diamonds.
Abstract: Reversed-zoned olivines (Fe-richer cores compared to rims), appear to be ubiquitous in kimberlites with a wide distribution. These olivines generally comprise a subordinate population relative to the dominant normally zoned olivines. However, they are notably more abundant in the megacryst-rich mid-Cretaceous Monastery and early Proterozoic Colossus kimberlites, located on the Kaapvaal and Zimbabwe cratons, respectively. The reverse-zoned olivines at these two localities define compositional fields that are closely similar to those for two olivine megacryst populations of the Cr-poor association which have been documented in the Monastery kimberlite. This points to a genetic link between megacrysts and the reversed zoned olivines. The ubiquitous, occurrence of the Fe-rich (relative to the field for rims) olivines in kimberlites with a wide geographic distribution in turn argues for an intimate link between megacrysts and the host kimberlite. Some large olivines have inclusions of rounded Cr-rich clinopyroxenes, garnets and/or spinel, characterized by fine-scale, erratic internal compositional zoning. Olivines with such chemically heterogeneous Cr-rich inclusions are not derived from disaggregated mantle peridotites, but are rather linked to the Cr-rich megacryst suite. Consequently, they cannot be used as evidence that cores of a majority of kimberlitic olivines are derived from disaggregated mantle peridotites.
Earth and Planetary Science Letters, Vol. 447, pp. 60-71.
Africa, South Africa
Deposit - Bultfontein
Abstract: Understanding the mineralogical controls on radiogenic chronometers is a fundamental aspect of all geochronological tools. As with other common dating tools, it has become increasingly clear that the Re -Os system can be impacted by multiple mineral formation events. The accessory and micrometric nature of the Re -Os-bearing minerals has made assessing this influence complex. This is especially evident in cratonic peridotites, where long residence times and multiple metasomatic events have created a complex melting and re-enrichment history. Here we investigate a harzburgitic peridotite from the Bultfontein kimberlite (South Africa) which contains sub-micron Pt -Fe-alloy inclusions within base metal sulphides (BMS). Through the combination of the focused ion beam lift-out technique and low blank mass spectrometry we were able to remove and analyse the Pt -Fe-alloy inclusions for their Re -Os composition and highly siderophile element (HSE) systematics. Six repeats of the whole-rock yield 187Os/188Os compositions of 0.10893 -0.10965, which correspond to Re depletion model ages (TRD) of 2.69 -2.79 Ga. The Os, Ir and Pt concentrations are slightly variable across the different digestions, whilst Pd and Re remain constant. The resulting HSE pattern is typical of cratonic peridotites displaying depleted Pt and Pd. The Pt -Fe-alloys have PUM-like 187Os/188Os compositions of 0.1294±24 (2-s.d.) and 0.1342±38, and exhibit a saw-tooth HSE pattern with enriched Re and Pt. In contrast, their BMS hosts have unradiogenic 187Os/188Os of 0.1084±6 and 0.1066±3, with TRD ages of 2.86 and 3.09 Ga, similar to the whole-rock systematics. The metasomatic origin of the BMS is supported by (i) the highly depleted nature of the mantle peridotite and (ii) their Ni-rich sulphide assemblage. Occurrence of Pt -Fe-alloys as inclusions within BMS grains demonstrates the genetic link between the BMS and Pt -Fe-alloys and argues for formation during a single but continuous event of silicate melt percolation. While the high solubility of HSE within sulphide mattes rules out early formation of the alloys from a S-undersaturated silicate melt and subsequent scavenging in a sulphide matte, the alignment of the Pt -Fe-alloy inclusions attests that they are exsolutions formed during the sub-solidus re-equilibration of the high temperature sulphide phases. The significant difference in 187Os/188Os composition between the included Pt -Fe-alloys and their BMS host can only be accounted for by different Re/Os. This suggests that the formation of Pt -Fe-alloy inclusions within a BMS can result in the fractionation of Re from Os. A survey experiment examining the partitioning of Re and Os confirmed this observation, with the Re/Os of the Pt -Fe-alloy inclusion up to ten times higher than the co-existing BMS. This fractionation implies that, when Re is present in the sulphide melt, the TRD ages of BMS containing alloy inclusions do not date the loss of Re due to partial melting, but rather its fractionation into the Pt -Fe-alloys. As such, BMS ages should be used with caution when dating ancient partial melting events.
Contributions to Mineralogy and Petrology, in press available 25p.
Canada, Northwest Territories
Deposit - Lac de Gras
Abstract: Megacrystic (>1 cm) clinopyroxene (Cr-diopside) and garnet (Cr-pyrope) xenocrysts within kimberlites from Lac de Gras (Northwest Territories, Canada) contain fully crystallized melt inclusions. These ‘polymineralic inclusions’ have previously been interpreted to form by necking down of melts at mantle depths. We present a detailed petrographical and geochemical investigation of polymineralic inclusions and their host crystals to better understand how they form and what they reveal about the evolution of kimberlite melt. Genetically, the megacrysts are mantle xenocrysts with peridotitic chemical signatures indicating an origin within the lithospheric mantle (for the Cr-diopsides studied here ~4.6 GPa, 1015 °C). Textural evidence for disequilibrium between the host crystals and their polymineralic inclusions (spongy rims in Cr-diopside, kelyphite in Cr-pyrope) is consistent with measured Sr isotopic disequilibrium. The preservation of disequilibrium establishes a temporal link to kimberlite eruption. In Cr-diopsides, polymineralic inclusions contain phlogopite, olivine, chromite, serpentine, and calcite. Abundant fluid inclusion trails surround the inclusions. In Cr-pyropes, the inclusions additionally contain Al-spinel, clinopyroxene, and dolomite. The major and trace element compositions of the inclusion phases are generally consistent with the early stages of kimberlite differentiation trends. Extensive chemical exchange between the host phases and the inclusions is indicated by enrichment of the inclusions in major components of the host crystals, such as Cr2O3 and Al2O3. This chemical evidence, along with phase equilibria constraints, supports the proposal that the inclusions within Cr-diopside record the decarbonation reaction: dolomitic melt + diopside ? forsterite + calcite + CO2, yielding the observed inclusion mineralogy and producing associated (CO2-rich) fluid inclusions. Our study of polymineralic inclusions in megacrysts provides clear mineralogical and chemical evidence for an origin of kimberlite that involves the reaction of high-pressure dolomitic melt with diopside-bearing mantle assemblages producing a lower-pressure melt that crystallizes a calcite-dominated assemblage in the crust.
Abstract: The comprehensive petrographical, petrochemical and mineralogical study of the Kovdor magnetite-apatite-baddeleyite deposit in the phoscorite-carbonatite complex (Murmansk Region, Russia) revealed a spatial distribution of grain size and chemical composition of three economically extractable minerals — magnetite, apatite, and baddeleyite, showing that zonal distribution of mineral properties mimics both concentric and vertical zonation of the carbonatite-phoscorite pipe.The marginal zone of the pipe consists of (apatite)-forsterite phoscorite carrying fine grains of Ti-Mn-Si-rich magnetite with ilmenite exsolution lamellae, fine grains of Fe-Mg-rich apatite and finest grains of baddeleyite, enriched in Mg, Fe, Si and Mn. The intermediate zone accommodates carbonate-free magnetite-rich phoscorites that carry medium to coarse grains of Mg-Al-rich magnetite with exsolution inclusions of spinel, medium-grained pure apatite and baddeleyite. The axial zone hosts carbonate-rich phoscorites and phoscorite-related carbonatites bearing medium-grained Ti-V-Ca-rich magnetite with exsolution inclusions of geikielite-ilmenite, fine grains of Ba-Sr-Ln-rich apatite and comparatively large grains of baddeleyite, enriched in Hf, Ta, Nb and Sc. The collected data enable us to predict such important mineralogical characteristics of the multicomponent ore as chemical composition and grain size of economic and associated minerals, presence of contaminating inclusions, etc. We have identified potential areas of maximum concentration of such by-products as scandium, niobium and hafnium in baddeleyite and REEs in apatite.
Abstract: Diamonds in alluvial deposits in Southeast Asia are not accompanied by indicator minerals suggesting primary kimberlite or lamproite sources. The Meratus Mountains in Southeast Borneo (Province Kalimantan Selatan, Indonesia) provide the largest known deposit of these so-called “headless” diamond deposits. Proposals for the origin of Kalimantan diamonds include the adjacent Meratus ophiolite complex, ultra-high pressure (UHP) metamorphic terranes, obducted subcontinental lithospheric mantle and undiscovered kimberlite-type sources. Here we report results from detailed sediment provenance analysis of diamond-bearing Quaternary river channel material and from representative outcrops of the oldest known formations within the Alino Group, including the diamond-bearing Campanian-Maastrichtian Manunggul Formation. Optical examination of surfaces of diamonds collected from artisanal miners in the Meratus area (247 stones) and in West Borneo (Sanggau Area, Province Kalimantan Barat;
Canadian Institute of Mining and Metallurgy, Vol. 6, 3, 14p.
Africa, Botswana
Deposit - Orapa
Abstract: The degree of uncertainty associated with a natural diamond resource is important to quantify from the time of discovery through the production lifetime. Data collection occurs during the discovery, exploration, delineation, and production or recovery phases. Quantifying the relationship between data and uncertainty is an important component of project valuation. The value of data is measured as their potential to reduce uncertainty if they are collected. A method is developed using Monte Carlo simulation for predicting resource uncertainty and valuing data during critical phases of development, particularly discovery and exploration. The technique is applied to diamond pipe deposits.
Abstract: In this work we report for the first time the crystallographic orientations of olivine inclusions trapped in diamonds from the Kaapvaal craton (South Africa) determined by single-crystal X-ray diffraction, and analyze them together with all available data in the literature. The overall data set indicates no preferred orientation of the olivine inclusions with respect to their diamond hosts. However, diamonds containing multiple olivine inclusions sometimes show clusters of olivines with the same orientation in the same diamond host. We conclude that such clusters can only be interpreted as the remnants of single olivine crystals pre-dating the growth of the host diamonds.
Abstract: In this work we report for the first time the crystallographic orientations of olivine inclusions trapped in diamonds from the Kaapvaal craton (South Africa) determined by single-crystal X-ray diffraction, and analyze them together with all available data in the literature. The overall data set indicates no preferred orientation of the olivine inclusions with respect to their diamond hosts. However, diamonds containing multiple olivine inclusions sometimes show clusters of olivines with the same orientation in the same diamond host. We conclude that such clusters can only be interpreted as the remnants of single olivine crystals pre-dating the growth of the host diamonds.
Abstract: In this work we report for the first time the crystallographic orientations of olivine inclusions trapped in diamonds from the Kaapvaal craton (South Africa) determined by single-crystal X-ray diffraction, and analyze them together with all available data in the literature. The overall data set indicates no preferred orientation of the olivine inclusions with respect to their diamond hosts. However, diamonds containing multiple olivine inclusions sometimes show clusters of olivines with the same orientation in the same diamond host. We conclude that such clusters can only be interpreted as the remnants of single olivine crystals pre-dating the growth of the host diamonds.
Abstract: We describe a new methodology to collect energy domain Mössbauer spectra of inclusions in natural diamonds using a Synchrotron Mössbauer Source (SMS). Measurements were carried out at the Nuclear Resonance beamline ID18 at the European Synchrotron Radiation Facility (Grenoble, France). We applied this non-destructive approach to collect SMS spectra of a ferropericlase inclusion still contained within its diamond host from Juina (Brazil). The high spatial resolution of the measurement (~ 15 ?m) enabled multiple regions of the 190 × 105 ?m2 inclusion to be sampled and showed that while Fe3 +/Fetot values in ferropericlase were below the detection limit (0.02) overall, there was a magnetic component whose abundance varied systematically across the inclusion. Hyperfine parameters of the magnetic component are consistent with magnesioferrite, and the absence of superparamagnetism allows the minimum particle size to be estimated as ~ 30 nm. Bulk Fe3 +/Fetot values are similar to those reported for other ferropericlase inclusions from Juina, and their variation across the inclusion can provide constraints on its history.
Abstract: Diamonds form from fluids or melts circulating at depth in the Earth's mantle. Analysis of these fluids is possible if they remain entrapped in the diamond during its growth, but this is rarely observed in gem-quality stones. We provide the first evidence that typical mineral inclusions in gem-quality diamonds from the Siberian and Kaapvaal cratons are surrounded by a thin film of hydrous silicic fluid of maximum thickness 1.5 ?m. The fluid contains Si2O(OH)6, Si(OH)4, and molecular H2O and was identified using confocal micro-Raman spectroscopy and synchrotron-based X-ray tomographic microscopy. As the solid mineral inclusions have both peridotitic and eclogitic affinities and occur in two cratonic regions, our results demonstrate the strong connection between water-rich fluids and the growth of gem-quality lithospheric diamonds. The presence of the fluid films should be taken into account for a proper evaluation of H2O contents in the mantle based on H2O contents in solid inclusions and for a robust assessment of diamond formation pressures based on the residual pressures of the inclusions.
Abstract: Fluids are now thought to be the growth medium for most diamonds sampled from the base of the lithosphere. Fluids trapped in fast-growing, fluid-rich diamonds provide the only direct view of this growth medium and provide valuable information on the geochemistry of deep mantle fluids in general. The most common fluids within fluid-rich diamonds are those belonging to the low- and high-Mg carbonatite affinity as well as more Si-rich variants. A sub-class of fluids that are very rich in alkalis and Cl, known as “saline” fluids, have been found but are generally scarce. At both Ekati and Diavik saline fluids appear much more common and provide a unique insight into their origin. We describe a novel sampling method that allows the analysis of the trace element and radiogenic isotope composition of diamonds (both gem and fluid-rich). Using these methods we analyzed 11 diamonds from the Fox kimberlite in the Ekati kimberlite cluster. The diamonds containing saline fluids are solely associated with peridotite on the basis of their micro-mineral inclusions. Silicic fluid compositions are related exclusively to eclogitic inclusions. Striking differences between the two fluid compositions are the positive Eu and Sr anomalies within saline fluids versus no anomalies in the silicic fluids. These characteristics are identical to previously studied fluids in fibrous diamonds from neighbouring kimberlites in Ekati and Diavik, which also contains diamonds carrying high- and low-Mg carbonatitic fluids. Combining the data, we show a clear chemical evolutionary trend, identifying for the first time saline fluids as parental to silicic and carbonatitic deep mantle melts, via fluid-rock interaction in the Slave CLM. Moreover, the trace-element and Sr isotopic fingerprints of subducting slabs and the timing of host diamond formation suggest that a subducting plate under western North America is the source of the saline fluids, which controlled metasomatism in the Slave lithosphere prior to Mesozoic kimberlite eruption. Saline fluids can be documented as a metasomatic product interacting with the lithosphere above shallow-subducting slabs such as the Farallon slab. As such they appear to be key players in the enrichment of the base of the lithosphere and the formation of diamonds.
Abstract: Fluids are now thought to be the growth medium for most diamonds sampled from the base of the lithosphere. Fluids trapped in fast-growing, fluid-rich diamonds provide the only direct view of this growth medium and provide valuable information on the geochemistry of deep mantle fluids in general. The most common fluids within fluid-rich diamonds are those belonging to the low- and high-Mg carbonatite affinity as well as more Si-rich variants. A sub-class of fluids that are very rich in alkalis and Cl, known as “saline” fluids, have been found but are generally scarce. At both Ekati and Diavik saline fluids appear much more common and provide a unique insight into their origin. We describe a novel sampling method that allows the analysis of the trace element and radiogenic isotope composition of diamonds (both gem and fluid-rich). Using these methods we analyzed 11 diamonds from the Fox kimberlite in the Ekati kimberlite cluster. The diamonds containing saline fluids are solely associated with peridotite on the basis of their micro-mineral inclusions. Silicic fluid compositions are related exclusively to eclogitic inclusions. Striking differences between the two fluid compositions are the positive Eu and Sr anomalies within saline fluids versus no anomalies in the silicic fluids. These characteristics are identical to previously studied fluids in fibrous diamonds from neighbouring kimberlites in Ekati and Diavik, which also contains diamonds carrying high- and low-Mg carbonatitic fluids. Combining the data, we show a clear chemical evolutionary trend, identifying for the first time saline fluids as parental to silicic and carbonatitic deep mantle melts, via fluid-rock interaction in the Slave CLM. Moreover, the trace-element and Sr isotopic fingerprints of subducting slabs and the timing of host diamond formation suggest that a subducting plate under western North America is the source of the saline fluids, which controlled metasomatism in the Slave lithosphere prior to Mesozoic kimberlite eruption. Saline fluids can be documented as a metasomatic product interacting with the lithosphere above shallow-subducting slabs such as the Farallon slab. As such they appear to be key players in the enrichment of the base of the lithosphere and the formation of diamonds.
Abstract: The composition of volatiles from fluid and melt inclusions in olivine phenocrysts from Yakutian kimberlite pipes of various ages (Olivinovaya, Malokuonapskaya, and Udachnaya-East) were studied for the first time by gas chromatography-mass spectrometry. It was shown that hydrocarbons and their derivatives, as well as nitrogen-, halogen-, and sulfur-bearing compounds, played a significant role in the mineral formation. The proportion of hydrocarbons and their derivatives in the composition of mantle fluids could reach 99%, including up to 4.9% of chlorineand fluorine-bearing compounds.
Abstract: The composition of volatiles from fluid and melt inclusions in olivine phenocrysts from Yakutian kimberlite pipes of various ages (Olivinovaya, Malokuonapskaya, and Udachnaya-East) were studied for the first time by gas chromatography-mass spectrometry. It was shown that hydrocarbons and their derivatives, as well as nitrogen-, halogen-, and sulfur-bearing compounds, played a significant role in the mineral formation. The proportion of hydrocarbons and their derivatives in the composition of mantle fluids could reach 99%, including up to 4.9% of chlorineand fluorine-bearing compounds.
Abstract: The results of morphological examination and the character of the structural orientation and estimation of residual pressure calculated from spectra of combination dispersion in olivine inclusions within diamonds of the Ebelyakh placer and kimberlite pipes of the Yakutian Diamondiferous Province are presented. The data analysis aimed at revealing indications of similarity and/or differences between diamonds from the pipes and the placer. Differences in the structural orientation and spectra of combination dispersion of the inclusions of olivine in dodecahedroids of placers of the northeastern part of the Siberian Platform support the assumption of their non-kimberlite nature.
Abstract: The results of morphological examination and the character of the structural orientation and estimation of residual pressure calculated from spectra of combination dispersion in olivine inclusions within diamonds of the Ebelyakh placer and kimberlite pipes of the Yakutian Diamondiferous Province are presented. The data analysis aimed at revealing indications of similarity and/or differences between diamonds from the pipes and the placer. Differences in the structural orientation and spectra of combination dispersion of the inclusions of olivine in dodecahedroids of placers of the northeastern part of the Siberian Platform support the assumption of their non-kimberlite nature.
Abstract: The results of morphological examination and the character of the structural orientation and estimation of residual pressure calculated from spectra of combination dispersion in olivine inclusions within diamonds of the Ebelyakh placer and kimberlite pipes of the Yakutian Diamondiferous Province are presented. The data analysis aimed at revealing indications of similarity and/or differences between diamonds from the pipes and the placer. Differences in the structural orientation and spectra of combination dispersion of the inclusions of olivine in dodecahedroids of placers of the northeastern part of the Siberian Platform support the assumption of their non-kimberlite nature.
Exploration Geophysics , http://dx.doi.org/10.1071/EG16015 10p. Available
Russia
Deposit Amakinskaya, Geophysics
Abstract: There have been multiple occurrences in the literature in the past several years of what has been referred to as the induced polarisation (IP) effect in airborne time domain electromagnetic (TDEM) data. This phenomenon is known to be responsible for incorrect inversion modelling of electrical resistivity, lower interpreted depth of investigation (DOI) and lost information about chargeability of the subsurface and other valuable parameters. Historically, there have been many suggestions to account for the IP effect using the Cole-Cole model. It has been previously demonstrated that the Cole-Cole model can be effective in modelling synthetic TDEM transients. In the current paper we show the possibility of extracting IP information from airborne TDEM data using this same concept, including inverse modelling of chargeability from TDEM data collected by VTEM, with field examples from Canada (Mt Milligan deposit) and Russia (Amakinskaya kimberlite pipe).
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 14p.
Africa, Lesotho
Deposit - Letseng
Abstract: Bateman Engineering managed the establishment of a second diamond treatment plant at the Letseng Mine in the Mokhotlong District of northern Lesotho, about 100 km from the town of Buthe Buthe. Letseng Diamonds Proprietary Limited, is owned 70 % by Gem Diamonds and 30 % by the Government of the Kingdom of Lesotho. The second plant, which commenced construction in late 2006, doubled Letseng Mines' hard rock processing capacity from 2.6 million t/yr to 5.2 million t/yr, making it the worlds' seventh largest diamond mine by throughput. Bateman Engineering provided the engineering design, procurement and construction management of the new plant.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 14p.
Africa, South Africa
Deposit - Cullinan
Abstract: There are many underground mining software tools available to plan and schedule the development of underground mines. A shortfall of these tools is the optimization of the underground equipment and strategy in order to maximize the development rate. This paper will illustrate how the SimMine® software was used to maximize underground development at Petra Diamonds' Cullinan Diamond Mine. It will also determine the effect of various development strategies and equipment capacities on the underground development rate and pinpoint potential bottlenecks in the mine development cycle.
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The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 12p.
Africa, South Africa
Deposit - Venetia
Abstract: The nature of diamond deposits are such that most mineral resource reporting codes contain a sub-section unique to diamond estimation and classification. These codes identify a number of criteria which define the uniqueness of diamond deposits, including, the low and variable grade of diamond deposits; the particulate nature of diamonds which affects both size and revenue of individual particles and finally the inherent difficulties and uncertainties in the estimation of diamond resources. These criteria are expanded on to provide an overview of the estimation of kimberlite diamond deposits. Placer deposits have been excluded as they constitute a particularly complex example of particulate distributions. Diamond grade, typically of the order of parts per million (ppm), is dependent on the number of stones per unit volume or mass as well as the diamond size distribution while diamond revenue is dependent on size, model, colour and quality. These parameters of a discrete particle result in a conmlOdily which requires some unique estimation and modelling methodologies. For most commodities "grade" is a measure of concentration and is directly proportional to value. [n the case of diamonds however the same stone grade (e.g. stones per 100 tonnes) may have significantly different carat grades and revenue, depending on the characteristics of the individual stones (size, model, colour and quality). The De _Beers Consolidated Mines Venetia Mine is used as an example of diamond eslimation as well as to highlighl some propriety grade eslimation techniques. The mine has been sampled for grade using a number of different sample supports, from 36" diameter reverse circulation drillholes to micro diamond core drilling. De Beers Group Services (Ply) Lld (DBGS) have developed a technique of mixed (or multiple) support kriging which allows for the combination of samples of different sizes (and therefore grade distributions) in the estimation process. In addition DBGS have researched techniques of both global and local grade estimation using micro diamonds. The estimation of kimberlite diamond deposits has a number of unique components resulting from the discrete nature of the diamond distribution. It is however equally fundamentally important to understand exactly what the sampling data represents; the constraints Wlder which the data were coUected (e.g. bottom cut ofJ) and the adjustments necessary to ensure parity Page 73 The Southern African Institute of Mining and Metallurgy Diamonds - Source to Use 2010 DBush between and within sampling programmes as well as the likely metallurgical process III a production environment.
Abstract: We report groundmass perovskite U -Pb (SIMS) ages, perovskite Nd isotopic (LA-ICPMS) composition and bulk-rock geochemical data of the Timmasamudram diamondiferous kimberlite cluster, Wajrakarur kimberlite field, in the Eastern Dharwar craton of southern India. The kimberlite pipes gave similar Mesoproterozoic ages of 1086 ± 19 Ma (TK-1, microcrystic variant) and 1119 ± 12 Ma (TK-3). However, a perovskite population sampled from the macrocrystic variant of TK-1 gave a much younger Late Cretaceous age of ca. 90 Ma. This macrocrystic kimberlite phase intrudes the Mesoproterozoic microcrystic phase and has a distinct bulk-rock geochemistry. The Nd-isotope composition of the ~ 1100 Ma perovskites in the cluster show depleted ?Nd(T) values of 2.1 ± 0.6 to 6.7 ± 0.3 whereas the ~ 90 Ma perovskites have enriched ?Nd(T) values of ? 6.3 ± 1.3. The depleted-mantle (DM) model age of the Cretaceous perovskites is 1.2 Ga, whereas the DM model age of the Proterozoic perovskites is 1.2 to 1.5 Ga. Bulk-rock incompatible trace element ratios (La/Sm, Gd/Lu, La/Nb and Th/Nb) of all Timmasamudram kimberlites show strong affinity with those from the Cretaceous Group II kimberlites from the Bastar craton (India) and Kaapvaal craton (southern Africa). As the Late Cretaceous age of the younger perovskites from the TK-1 kimberlite is indistinguishable from that of the Marion hotspot-linked extrusive and intrusive igneous rocks from Madagascar and India, we infer that all may be part of a single Madagascar Large Igneous Province. Our finding constitutes the first report of Cretaceous kimberlite activity from southern India and has significant implications for its sub-continental lithospheric mantle evolution and diamond exploration programs.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 8p.
Africa, Botswana
Deposit - AK6
Abstract: The AK6 kimberlite is situated 25 km south of the Debswana Orapa Mine in Botswana and was discovered by De Beers geologists in 1969 during the follow-up of geophysical targets in the Orapa area. The kimberlite was not extensively pursued at the time as the initial bulk sampling indicated it to be of limited size and low grade, factors largely contributed to by the basalt breccia capping. Completion of high resolution integrated geophysical techniques and drill bulk sampling to depth recovered 97 tons of kimberlite during 2003 and 2004, which led to the increased size and grade estimates. Bulk sampling by Large Diameter Drilling (LDD, 23 inch diameter) commenced in 2005; 13 holes were drilled to a cumulative depth of 3,699 m and 689 carats of diamonds were recovered. In July 2006 the De Beers Mineral Resource Classification Committee classified these Phase I LOO results at a High Inferred level with an average grade of 24 carats per hundred tonnes (cpht) at a bottom cut-off of +1 mm, and a modeled average diamond value of 150 dollars per carat. A second phase of LDO drilling was initiated in 2006, and bulk sampling by trenching commenced in 2007 in order to deliver a resource estimate at indicated level. An Indicated Resource of 11.1 million carats at an average grade of 22 cpht was declared for the deposit mining lease application lodged in 2007.
Abstract: Using stable isotope data obtained on multiple aliquots of diamonds from worldwide sources, it has been argued that carbon and nitrogen in diamond are decoupled. Here we re-investigate the carbon-nitrogen relationship based on the most comprehensive microbeam data set to date of stable isotopes and nitrogen concentrations in diamonds (n = 94) from a single locality. Our diamond samples, derived from two kimberlites in the Chidliak Field (NE Canada), show large variability in ?13C (? 28.4 ‰ to ? 1.1‰, mode at ? 5.8‰), ?15N (? 5.8 to + 18.8‰, mode at ? 3.0‰) and nitrogen contents ([N]; 3800 to less than 1 at.ppm). In combination, cathodoluminescence imaging and microbeam analyses reveal that the diamonds grew from multiple fluid pulses, with at least one major hiatus documented in some samples that was associated with a resorption event and an abrupt change from low ?13C and [N] to mantle-like ?13C and high [N]. Overall, ?13C appears to be uncorrelated to ?15N and [N] on both the inter- and intra-diamond levels. Co-variations of ?15N-log[N], however, result in at least two parallel, negatively correlated linear arrays, which are also present on the level of the individual diamonds falling on these two trends. These arrays emerge from the two principal data clusters, are characterized by slightly negative and slightly positive ?15N (about ? 3 and + 2‰, respectively) and variable but overall high [N]. Using published values for the diamond-fluid nitrogen isotope fractionation factor and nitrogen partition coefficient, these trends are perfectly reproduced by a Rayleigh fractionation model. Overall, three key elements are identified in the formation of the diamond suite studied: (1.) a low ?13C and low [N] component that possibly is directly associated with an eclogitic diamond substrate or introduced during an early stage fluid event. (2.) Repeated influx of a variably nitrogen-rich mantle fluid (mildly negative ?13C and ?15N). (3.) In waning stages of influx, availability of the mantle-type fluid at the site of diamond growth became limited, leading to Rayleigh fractionation. These fractionation trends are clearly depicted by ?15N-[N] but are not detected when examining co-variation diagrams involving ?13C. Also on the level of individual diamonds, large (? 5‰) variations in ?15N are associated with ?13C values that typically are constant within analytical uncertainty. The much smaller isotope fractionation factor for carbon (considering carbonate- or methane-rich fluids as possible carbon sources) compared to nitrogen leads to an approximately one order of magnitude lower sensitivity of ?13C values to Rayleigh fractionation processes (i.e. during fractionation, a 1‰ change in ?13C is associated with a 10‰ change in ?15N). As a consequence, even minor heterogeneity in the primary isotopic composition of diamond forming carbon (e.g., due to addition of minor subducted carbon) will completely blur any possible co-variations with ?15N or [N]. We suggest this strong difference in isotope effects for C and N to be the likely cause of observations of an apparently decoupled behaviour of carbon and nitrogen isotopes in diamond.
Abstract: Olivine is the dominant mineral present in kimberlite magmas; however, due to the volatile-rich nature of most kimberlites, they rarely survive late-stage serpentinisation. Here we present major and trace element data for a rare example of ultra-fresh olivine in a macrocrystic calcite kimberlite from the Benfontein kimberlite sill complex. Olivines are characterised by xenocrystic cores surrounded by multiple growth zones representing melt crystallisation and late-stage equilibration. Two distinct core populations are distinguished: Type 1) low Fo (88-89), Ni-rich, Ca- and Na-rich cores, interpreted here to be the result of carbonate-silicate metasomatism potentially as part of the earliest stages of kimberlite magmatism, and Type 2) high Fo (91-93), Ni-rich, low-Ca cores derived from a typical garnet peridotite mantle source. In both cases, the cores have transitional margins (Fo89-90) representing equilibration with a proto-kimberlite melt. Trace element concentrations, in particular Cr, of these transition zones suggest formation of the proto-kimberlite melt through assimilation of orthopyroxene from the surrounding garnet peridotite lithology. Trace element trends in the surrounding melt-zone olivine (Fo87-90) suggest evolution of the kimberlite through progressive olivine crystallisation. The final stages of olivine growth are represented by Fe-rich (Fo85) and P-rich olivine indicating kimberlite evolution to mafic compositions. Fine (< 60 ?m), Mg-rich olivine rims (Fo94-98) represent equilibration with the final stages of kimberlite evolution back to Fe-poor carbonatitic melts. We present a step-by-step model for kimberlite magma genesis and evolution from mantle to crust tracked by the chemistry of olivines in the Benfontein kimberlite. These steps include early stages of metasomatism and mantle assimilation followed by direct crystallisation of the kimberlite melt and late-stage equilibration with the evolved carbonatitic residual liquids. The Ca contents of the Type 1 xenocrystic olivines are the highest yet measured for mantle olivines, and do not overlap with any known mantle xenolith lithologies. These olivines likely represent an important stage of metasomatism directly related to the early stages of kimberlite melt ponding at the base of the lithospheric mantle.
Abstract: Here we present major and trace element data for garnet and clinopyroxene from mantle-derived peridotite xenoliths of the Grib kimberlite, the Arkhangelsk diamond province, Russia, and provide new insights into the metasomatic processes that occur within the subcontinental lithospheric mantle (SCLM) during the kimberlite generation and ascent. The mantle xenoliths examined in this study are both coarse and sheared garnet peridotites and consist of olivine, orthopyroxene, clinopyroxene, garnet with minor ilmenite, magnetite, and Cr-spinel. Based on garnet and clinopyroxene composition, two groups of peridotite are recognized. One group contains high-Ti, light rare earth elements (LREE) enriched garnets and low-Mg# clinopyroxenes with low (La/Sm)n (C1 chondrite-normalized) values. This mineral assemblage was in equilibrium with a high-temperature carbonate-silicate metasomatic agent, presumably, a protokimberlite melt. Pressure-temperature (P-T) estimates (T = 1220 °C and P = 70 kbar) suggest that this metasomatic event occurred at the base of the SCLM. Another group contains low-Ti garnet with normal to sinusoidal rare earth elements (REE) distribution patterns and high-Mg# clinopyroxenes with wide range of (La/Sm)n values. The geochemical equilibrium between garnet and clinopyroxene coupled with their REE composition indicates that peridotite mantle experienced metasomatic transformation by injection of a low-Ti (after crystallizations of the ilmenite megacrysts) kimberlite melt that subsequently percolated through a refractory mantle column. Peridotites of this group show a wide range of P-T estimates (T = 730-1070 °C and P = 22-44 kbar). It is suggested that evolution of a kimberlite magma from REE-enriched carbonate-bearing to carbonate-rich ultramafic silicate compositions with lower REE occurs during the ascent and interaction with a surrounding lithospheric mantle, and this process leads to metasomatic modification of the SCLM with formation of both high and low-Ti garnets and clinopyroxene widely varying in Mg# and (La/Sm)n values.
Journal of Volcanology and Geothermal Research, in press available 19p.
Russia
Deposit - Udachnaya East
Abstract: The Udachnaya East kimberlite is characterized by the presence of chlorides, sulfates and alkali carbonates. This highly atypical mineralogy underpinned a model for an anhydrous alkali-rich primary kimberlite melt, despite the absence of petrographic studies providing textural context to the exotic minerals. The present work documents the petrography of the Udachnaya East kimberlite in order to address this problem. The pipe comprises two varieties of Fort-a-la-Corne type pyroclastic kimberlite, olivine-rich and magmaclast-rich, and coherent kimberlite. These kimberlites entrain xenoliths of limestones, altered shales and siltstones, halite-dominated rocks, dolomites, and coarse calcite rocks. The distinct varieties of the Udachnaya East kimberlite carry different populations of crustal xenoliths, which partially control the mineralogy of the host kimberlite. In magmaclast-rich pyroclastic kimberlite, where halite is absent from the crustal xenoliths, it is not observed in the interclast matrix, or within the magmaclasts. Halite occurs in the interclast matrix of olivine-rich pyroclastic kimberlite, where halite xenoliths are common. Large, ~ 30 cm halite xenoliths are uniquely restricted to the coherent kimberlite and show a strong reaction with it. The halite xenoliths are sourced from depths of ? 1500 to ? 630 m, where carbonate beds host multiple karst cavities filled with halite and gypsum and occasional sedimentary evaporites. The style of secondary mineralization at Udachnaya depends on whether the kimberlite is coherent or pyroclastic. Shortite, pirssonite and other alkali carbonates replacing calcite and possibly serpentine are abundant only in porous pyroclastic kimberlites of both types and in their shale/siltstone xenoliths. The lower porosity of the coherent kimberlite prevented the interaction of kimberlite with Na brines. Serpentinization localized around halite xenoliths started at temperatures above 500 °C, as indicated by its association with high-temperature iowaite. The model of the “dry” Na and Cl-rich primary kimberlite melt is invalidated on the basis of 1) the restriction of exotic salt minerals to certain kimberlite types and xenoliths; and 2) the absence of halite-rich melt inclusions in olivine of coherent kimberlite.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 18p.
Africa, South Africa
Deposit - Finsch
Abstract: Finsch Mine is a kimberlite diamond mine located at Lime Acres in the Northern Cape Province of South Africa. The mine was founded in 1961 and started surface mining in 1964. Underground production commenced in 1990 using a modified blast-hole open stoping method for the mining of Blocks 1, 2 and 3. Block 4 is currently being mined as a block cave. The process of identifying and optimizing a method to mine the Block 5 orebody started in 1991, and in 2006 incline caving was identified as being technically feasible. This paper aims to document the process employed in developing this method by the Block 5 pre-feasibility team as well as discuss the technical challenges encountered during this process. The paper commences with a history of Finsch Mine and highlights the complex geology and threat of sidewall failure that prompted the decision to use block caving as the mining method for Block 4. A literature study of mines that implemented mining methods upon which the incline cave was conceptualized is then presented. These practices were then used to form the basis for the designs on which the initial geotechnical modelling was done and built upon through an iterative process of modelling and design changes. The ventilation of the mining area, initial productivity simulation results, and the applicability of automation and comminution processes in the incline cave are also presented. The paper concludes with an investigation into some of the challenges of the mining method, and shows that that incline caving is a technical option available for further investigation in determining the optimal mining method to be employed at Block 5, Finsch Diamond Mine.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 14p.
Africa, South Africa
Deposit - Finsch
Abstract: De Beers' Finsch Mine is situated in the Northern Cape ,province, 170 km northwest of Kimberley. The concentrator facility, designed and constructed by Bateman Engineering, was commissioned in 1967 and upgraded in 1979 using diamond liberation and extraction technology available at the time of design. Since then significant advances in diamond processing and technology have been made and these -have been incorporated into the new main treatment plant and recovery plant flowsheets, making diamond liberation and recovery from the Pre-1979 dumps a viable economic option at Finsch." Significant challenges were experienced as a result of the integration of new technology and its associated infrastructure into an existing plant. Major process flow changes were implemented during the execution phase of the project. The combined effect of these issues resulted in the project being overspent by 25% and the final handover to the Client was some 18 months later than originally planned." The paper highlights some of the difficulties experienced as a result of changes made during the execution phases of the project.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 28p.
Africa, Botswana
Deposit - Orapa
Abstract: Commencing with the Pre-Feasibility Study (PFS) conclusions, the Orapa 3 process design evolved through a phase of value-engineering studies. An overall re-evaluation of the originally proposed process design was necessary both in order to address the interim increase in target throughput from 9.8 Mtpa to 12 Mtpa as well as to increase capital efficiency. In the interests of clarity, the PFS process design for Orapa 3 has been omitted from this paper, as it is no longer relevant. Recognition is however due to those engaged in earlier phases of the Orapa 3 project with respect to fundamental mass~balancing modelling; and ore and diamond characterisation, which fanned the basis for the process design that has evolved from feasibility study activities. The background context for Orapa 3 is of an operation expected to yield operating utilisation and revenue improvements relative to the Orapa 2 operation. Delivering these without undue penalties to capital and operating cost required a shift in thinking, trading excess installed capacity for flexible circuit configuration. The process design adopted is "layered", with the purpose of preserving Run Of Mine (ROM) throughput by reducing in-circuit arisings - particularly to the Dense Medium Separation (DMS) section - rather than simply installing additional DMS capacity on the expectation of low DMS availability. Elsewhere, the ability to monitor and maintain critical sizing activities - particularly desanding - without impact on overall plant throughput is intended to motivate operators to avoid the temptation to trade quality for quantity. At present, since an overall dynamic simulation of the Orapa 3 operation has still to be carried out, the design mass balance has been based on a relatively onerous combination of worst case feed type with 100% front-line process capacity in all plant sections. This means that, whilst the installed DMS capacity is based on routing 100% of sized scrubbing section product directly to the DMS, and with one DMS module always unavailable, the High Pressure Rolls Crushing (HPRC) capacity is based on allowing for 50% of this stream to be instead routed first to the HPRC section, at no more than 75% of maximum roll speed for the two units installed. This is an obvious "belt and braces" approach. Following the dynamic simulation exercise (currently in progress), it is likely that a less conservative approach will be taken. This will not affect the conceptual design of the process plant, being mostly an exercise in refining the number of DMS modules to be installed, and possibly reducing slightly the size of the HPRC roll units. Both of these will have positive capital and operating cost impacts. Page 215 The Southern African Institute of Mining and Metallurgy Diamonds - Source to Use 2010 G Popp/ewell andB Hae/else DMS capacity, despite being split into coarse and fiaes streams, consists of identical modules. Two of the nine modules are set-up to receive either coarse or fine feed, the only difference being that fines modules are rated at lower capacity than the same modules treating coarse feed. Final recovery section capacity is based on entirely wet primary diamond recovery technology. This greatly reduces both the cost of drying. a large amount of recovery section feed and the dust• management issues associated with dry recovery technology. In contrast to the Orapa 2 operations, a scavenginglauditgrease belt section is included as a diamond recovery "goal-keeper" and to provide a process assurance function.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 10p.
Africa, Botswana
Deposit - Jwaneng
Abstract: Debswana's Jwaneng Mine (south-central Botswana) is the richest diamond mine• in the world and has been contributing substantial revenue to Botswana since the mine started operating in 1982. The resource consists of 3 separate volcanic pipes/vents namely North, South and Centre pipes (2 additional small kimberlite bodies have also been intersected within the mining pit) which erupted through Transvaal strata and the overlying Karoo sediments - 245 million years ago. Although earlier drilling and geophysical surveys suggest that the 3 pipes extend to depths greater than 1 km below the surface, the resource is only at an indicated level of confidence to a depth of 400m, and mining activities will start exploiting the inferred resource material below 400m in 2014.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 14p.
Canada, Quebec
Deposit - Renard
Abstract: The Renard kimberlite cluster is located in the Monts Otish region of Quebec, Canada. A Canadian National Instrument (NI) 43-101 compliant resource statement for the Renard kimberlites 2, 3, 4 and 9 and the Lynx kimberlite dyke was first issued in 2008 followed by a Preliminary Economic Assessment and the development of a conceptual mine plan. Following a successful drill program in 2009 tbat greatly expanded the amount of kimberlite in Renard 2, a revised resource statement was issued in December 2009 comprising 23 mitlion carats of Indicated Mineral Resources and 13 million carats of Inferred Mineral Resources, a threefold increase on the previous estimate. The project is currently the focus of a second Preliminary Economic Assessment and it is expected that a full feasibility and permitting program will commence in 2010 leading to the creation of Quebec's first diamond mine by 2013
Abstract: Neoproterozoic kimberlite, ultramafic lamprophyre, and carbonatite magmatic activity was widespread across the Canadian-Greenland Shield. Models to explain the preponderance of this deeply-derived CO2-rich magmatism between 680-540 Ma range from impingement of multiple mantle plumes to rifting activity linked to the breakout of the Laurentian plate from the Rodinia supercontinent configuration. We add to the debate about the origin of kimberlite magmas and evaluate possible mantle sources of the 655 Ma ‘diamond-rich’ Renard (new SIMS U/Pb perovskite ages) and 629 Ma ‘barren’ Wemindji kimberlites on the eastern Superior craton in Quebec, Canada. Our Sr-Nd-Hf and carbon isotope data (87Sr/86Sri = 0.70241-0.70442; ?Ndi = + 0.2 to + 4.8; ?Hfi = + 0.3 to + 6.5; ?13C = ? 5.6 to ? 3.9‰) suggest a common and moderately depleted convecting upper mantle source region for both the Renard and Wemindji kimberlites, which occur 400-km apart in the interior of the Superior craton. In contrast, the low Os isotope ratios (187Os/188Osi = 0.11078-0.12620; ?Osi = ? 13.7 to ? 1.6) and unfractionated chondritic relative HSE abundances (Os, Ir, Ru, Pt, Pd, Re) indicate significant involvement of ancient refractory cratonic mantle material in kimberlite magma formation. Our model calculations suggest that for both the diamond-rich Renard and the barren Wemindji kimberlite magmas up to 30% of the Os was derived from refractory cratonic peridotites. This material might have been assimilated by originally more CO2-rich carbonated silicate melts derived from the asthenosphere. We also show that the geochemical and Sr-Nd-Hf-Os isotopic compositions of the Renard and Wemindji kimberlites do not require significant input from melts derived from olivine-poor cratonic mantle lithologies such as MARID-type veins and pyroxenites/eclogites. This contrasts with the petrogenesis of deeply-derived volatile-rich potassic magmas found along the peripheries of cratons (e.g., ultramafic lamprophyres, kamafugites, and olivine lamproites), a setting where abundant non-peridotitic components have been added to the lithospheric mantle over the course of continent evolution. Provided that CO2-rich melts, such as proto-kimberlites, occur near the solidus of volatile-fluxed peridotites, no excess mantle heat is required in their formation. This important but often overlooked constraint, together with the observation that there exist no spatial or temporal relationships between the Superior craton kimberlites and Large Igneous Provinces during the Late Neoproterozoic, suggests that kimberlite magmatic activity was tectonically controlled. In our preferred model, ubiquitous CO2-rich proto-kimberlite melts form during volatile-controlled redox melting processes at ambient mantle temperatures in a thermal boundary layer directly beneath thick cratonic lithosphere. The success rate of ‘evolving’ hybrid kimberlite magmas reaching Earth’s surface increases when tensile stresses propagate into the > 200 km thick keels of continental lithosphere. These conditions are frequently met during fast and changing plate motions associated with the assembly and breakup of supercontinents.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 18p.
Africa, Botswana
Deposit - Jwaneng
Abstract: Slope stability is a fundamental part of a successful mining operation. It impacts directly on the safety of personnel and the economics of the mine. The Jwaneng Mine in Botswana is planning a push back of 644m depth in the south east wall. Mining will commence in 2010 and be completed in 2024. This will put the mine in the deep pit category. The mine has invested in extensive geotechnical data gathering and design programs that started as far back as 2003 for the south east wall. The south east wail of Jwaneng Mine is characterized by foliation that dips adversely into the mining faces. The orienta1ion of the foliation is variable due to intense tectonic movements that have also caused the occurrence of faults that are sub-vertical. A considerable amount of information on the characteristics of structural patterns and the rock mass has been collected. This paper presents an overview of the feasibility level geotechnical design that is about to be concluded.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 12p.
Africa, South Africa
Deposit - Namaqualand mines
Abstract: Alluvial diamond deposits covered with a thick overburden cannot be explored effectively and mined profitably with the available conventional techniques. A novel directional drilling technique has been developed and site trials have been conducted at the e Beers Namaqualand Mines situated at the western coast of South Africa. This paper describes the technique developed as well as the results of the site trials. The main task of the project is to develop a tool and a supporting system to achieve a remote exploration and ore extraction method for inaccessible alluvial diamond deposits. The project involves the acquisition of a system, commissioning on-site and evaluating the information obtained during assessment. The project consists of the design - of certain tools and instrumentation for the system, investigations and desktop studies as well as development of the systems logistics. The operating philosophy of the system is based on the keyhole surgery principle. In this study a pilot hole was drilled first, starting from the surface with an inclination to reach deeply seated diamondiferous gravel layers, followed by drilling into a more or less horizontal gravel layer for a certain length and finally pointing-upwards reaching ground surface at a predetermined exit point. The pilot drill bit was then replaced with a larger diameter reamer/mining tool and an HDPE tail pipe was attached behind the reamer. The drill string was retracted back to enlarge the guide hole and flush the excavated ore to the surface through the tail pipe. The material flow in between the sections of the system was carefully measured to assess and record the gravel recovery rates. Several horizontal holes were drilled at preplanned drill paths to reach and follow the ore layer and the ore extraction was achieved by means of a reamer/mining tool. Principles of the concept have been proven viable in this investigation
Mine Water and the Environment, Vol. 35, pp. 350-368.
Canada, Northwest Territories
Deposit - Gahcho Kue
Abstract: Eight water models were used to assess potential aquatic environmental effects of the proposed Gahcho Kué diamond mine on groundwater and surface water flow and quality in the Northwest Territories, Canada. This sequence of models was required to cover different spatial and temporal domains, as well as specific physico-chemical processes that could not be simulated by a single model. Where their domains overlapped, the models were interlinked. Feedback mechanisms amongst models were addressed through iterative simulations of linked models. The models were used to test and refine mitigation plans, and in the development of aquatic component monitoring programs. Key findings generated by each model are presented here as testable hypotheses that can be evaluated after the mine is operational. This paper therefore offers a record of assumptions and predictions that can be used as a basis for post-validation.
Abstract: Kimberlitic magmaclasts are discrete ovoid magmatic fragments that formed prior to emplacement from disrupted kimberlite magma. To provide new constraints on the origin and evolution of the kimberlite melts, we document the mineralogy and petrography of a magmaclast recovered from one of the ca. 520 Ma Venetia kimberlites, South Africa. The sample (BI9883) has a sub-spherical shape and consists of a ~ 10 mm diameter central olivine macrocryst, surrounded by porphyritic kimberlite. The kimberlitic material consists of concentrically aligned, altered olivine phenocrysts, set in a crystalline groundmass of calcite, chromite, perovskite, phlogopite, apatite, ilmenite, titanite, sulphides, rutile and magnetite along with abundant alteration phases (i.e. serpentine, talc and secondary calcite). These features are typical of archetypal hypabyssal kimberlites. We examined primary fluid/melt inclusions in chromite, perovskite and apatite containing a diversity of daughter phases. Chromite and perovskite host polycrystalline inclusions containing abundant alkali-carbonates (i.e. enriched in K, Na, Ba, Sr), phosphates, Na-K chlorides, sulphides and equal to lesser quantities of olivine, phlogopite and pleonaste. In contrast, apatite hosts polycrystalline assemblages with abundant alkali-carbonates and Na-K chlorides and lesser amounts of olivine, monticellite and phlogopite. Numerous solid inclusions of shortite (Na2Ca2(CO3)3), Na-Sr-carbonates and apatite occur in groundmass calcite along with fluid inclusions containing daughter crystals of Na-carbonates and Na-chlorides. The primary inclusions in chromite, perovskite and apatite are considered to represent remnants of fluid(s)/melt(s) trapped during crystallisation of the host minerals, whereas the fluid inclusions in calcite are probably secondary in origin. The component proportions of these primary fluid/melt inclusions were estimated in an effort to constrain the composition of the evolving kimberlite melt. These estimates suggest melt evolution from a silicate-carbonate kimberlite melt that became increasingly enriched in carbonates, phosphates, alkalis and chlorides, in response to the fractional crystallisation of constituent minerals (i.e. olivine to apatite). The concentric alignment of crystals around the olivine kernel and ovoid shape of the magmaclast can be ascribed to the low viscosity of the kimberlite melt and rapid rotation whilst in a liquid or partial crystalline state, or to progressive layer-by-layer growth of the magmaclast. Although the mineralogy of our sample is similar to hypabyssal kimberlites worldwide, it differs from hypabyssal kimberlite units in the main Venetia pipes, which contain monticellite-phlogopite rich assemblages and segregationary matrix textures. Therefore magmaclast BI9883 probably originated from a batch of magma distinct from those that produced known hypabyssal units within the Venetia kimberlite cluster.-
Abstract: In this study, 660 diamonds from Igarapé Lajes Diggings (Roosevelt and Aripuanã Park indigenous areas), in Amazonian craton, Rondônia State, Brazil, were investigated. Their morphological, optical and surface characteristics were described using optical and scanning electron microscopy (SEM), cathodoluminescence (CL) and infrared spectroscopy (FTIR). The results demonstrated a predominance of resorbed crystals with many surface corrosion features, generally colorless, and led to the identification of four distinct groups: G1, G2, G3 and G4. Group G1 presents features of secondary sources while G2 and G4 show only primary features, some of which are not described in literature. Group G3 is similar to the other groups, however, is composed of less resorbed specimens with primary octahedral morphology relatively well preserved, indicating shorter time of exposure to dissolution effects. Cathodoluminescence in G2 is attributed to features of plastic deformation and to low contents of nitrogen (< 100 ppm, Type II) and high aggregation (IaB). G4 shows homogeneous blue CL, high contents of nitrogen (700 to 1000 ppm) and intermediate aggregation (IaAB). G1 presents luminescence influenced by radiation effects and populations with N contents and aggregation in the same ranges of G2 and G4, suggesting that the primary sources of the three groups can be the same. The relationship of nitrogen content versus aggregation state indicates higher temperatures of formation for G2 and lower for G4. The obtained data suggests that diamonds of G2 originated in sublithospheric mantle as has also been reported in nearby deposits (Machado River and Juína). The employed techniques were also effective in distinguishing diamonds from Roosevelt Reserve and from other localities, indicating that they could be used for improvement of certification procedures of diamonds of unknown origin.
Thesis, University of Pretoria, Ms Metallurgical Engineering 279p. Pdf
Africa, Angola, South Africa
Deposit - AC 56-5-1, Venetia Red
Abstract: Kimberlite is the host rock from which diamonds are mined. The mineralogical features for kimberlites vary greatly with country, origin, depth and type of kimberlite. Kimberlites can contain various clay species with some kimberlites containing predominantly clay minerals. The presence of these clay minerals in the ore can cause difficulty in dewatering due to high flocculant demand, poor supernatant clarity and low settling rates. Identifying critical parameters that can predict the settling behaviour of African kimberlite slurries will assist the process engineer to predict the settling behaviour of different kimberlite slurries. Especially identifying the kimberlites that will most likely not settle with normal flocculant dosage rates is useful. From first principles the settling of a particle is described by Stoke’s law which incorporates the density of the particle and size of the particle as the inherent particle variables. In this case density is assumed constant and therefore the size of particles influence the settling rate of particles to a great extent. This study therefore investigated the influence of particle size on settling rate and whether the particle size distribution showed correlation with settling rate when regression modelling was fitted on the data. Other variables that were tested for correlation with settling were pH when the kimberlite is mixed in water as well as various mineralogical features of the ore. Fitting a simple model to any of these properties or combinations of these properties was attempted which would allow for prediction of settling behaviour. The mineralogical features were classified by evaluating the mineral composition, fractional elemental analysis, cation exchange capacity and the exchangeable sodium percentage of the different kimberlites. These variables were tested as well as their settling behaviour with 18 different African kimberlite samples. The settling rate and slurry bed compaction during natural settling as well coagulant and flocculant assisted settling were measured for the kimberlite slurries. The best performing coagulant and flocculant for each kimberlite were combined to evaluate potential improvements in the settling rates and slurry bed compaction compared to current settling practices that only utilise flocculant additions. Especially the use of coagulant for kimberlites that did not show settling with only flocculants was evaluated. For these 18 kimberlites only 2 kimberlites did not settle with the use of flocculants with settling rates varying between 10.7m/h and 25m/h. Both these kimberlites also did not settle with the combination of coagulant and flocculant, but could only settle with only coagulant additions at settling rates of 1.9 m/h and 2.2 m/h. Regression analysis fitted to the settling rate investigated the influence of particle size, pH and mineralogical features on settling. For representation of the particle size two data points from the Particle Size Distribution (PSD) was utilised which represented the fine material and the coarser material. These two data points were taken at percentage passing 7.5 ?m and 75 ?m. Regression data for kimberlite with flocculant additions showed that particle size and the pH of the slurry were identified as significant parameters in predicting settling. The regression data showed a R2 of 0.78 for the settling rate and an adjusted R2 of 0.79 for the slurry bed depth.
Thesis, University of Pretoria, Ms Metallurgical Engineering 279p. Pdf
Africa, Angola, South Africa
Deposit - AC 56-5-1, Venetia Red
Abstract: Kimberlite is the host rock from which diamonds are mined. The mineralogical features for kimberlites vary greatly with country, origin, depth and type of kimberlite. Kimberlites can contain various clay species with some kimberlites containing predominantly clay minerals. The presence of these clay minerals in the ore can cause difficulty in dewatering due to high flocculant demand, poor supernatant clarity and low settling rates. Identifying critical parameters that can predict the settling behaviour of African kimberlite slurries will assist the process engineer to predict the settling behaviour of different kimberlite slurries. Especially identifying the kimberlites that will most likely not settle with normal flocculant dosage rates is useful. From first principles the settling of a particle is described by Stoke’s law which incorporates the density of the particle and size of the particle as the inherent particle variables. In this case density is assumed constant and therefore the size of particles influence the settling rate of particles to a great extent. This study therefore investigated the influence of particle size on settling rate and whether the particle size distribution showed correlation with settling rate when regression modelling was fitted on the data. Other variables that were tested for correlation with settling were pH when the kimberlite is mixed in water as well as various mineralogical features of the ore. Fitting a simple model to any of these properties or combinations of these properties was attempted which would allow for prediction of settling behaviour. The mineralogical features were classified by evaluating the mineral composition, fractional elemental analysis, cation exchange capacity and the exchangeable sodium percentage of the different kimberlites. These variables were tested as well as their settling behaviour with 18 different African kimberlite samples. The settling rate and slurry bed compaction during natural settling as well coagulant and flocculant assisted settling were measured for the kimberlite slurries. The best performing coagulant and flocculant for each kimberlite were combined to evaluate potential improvements in the settling rates and slurry bed compaction compared to current settling practices that only utilise flocculant additions. Especially the use of coagulant for kimberlites that did not show settling with only flocculants was evaluated. For these 18 kimberlites only 2 kimberlites did not settle with the use of flocculants with settling rates varying between 10.7m/h and 25m/h. Both these kimberlites also did not settle with the combination of coagulant and flocculant, but could only settle with only coagulant additions at settling rates of 1.9 m/h and 2.2 m/h. Regression analysis fitted to the settling rate investigated the influence of particle size, pH and mineralogical features on settling. For representation of the particle size two data points from the Particle Size Distribution (PSD) was utilised which represented the fine material and the coarser material. These two data points were taken at percentage passing 7.5 ?m and 75 ?m. Regression data for kimberlite with flocculant additions showed that particle size and the pH of the slurry were identified as significant parameters in predicting settling. The regression data showed a R2 of 0.78 for the settling rate and an adjusted R2 of 0.79 for the slurry bed depth.
Abstract: A VTEM survey was flown over the Drybones kimberlite in 2005, followed by a ZTEM survey in 2009. These data sets were inverted on multiple previous occasions using various 1D, 2D, 3D and plate modelling algorithms. VTEM data showed AIP effects, manifested as negative voltages and otherwise skewed transients. This created artefacts in conventional inversions of VTEM data, which showed some inconsistencies with ZTEM inversions, as well as with the known geology. In 2015 the VTEM data were transferred to Aarhus Geophysics, reprocessed and reinverted using the modified "AarhusINV" code with Cole-Cole modelling. The results are presented in current abstract, they appear to be more interpretable and provide better data fit, than previous inversion attempts.
Abstract: Using stable isotope data obtained on multiple aliquots of diamonds from worldwide sources, it has been argued that carbon and nitrogen in diamond are decoupled. Here we re-investigate the carbon-nitrogen relationship based on the most comprehensive microbeam data set to date of stable isotopes and nitrogen concentrations in diamonds (n = 94) from a single locality. Our diamond samples, derived from two kimberlites in the Chidliak Field (NE Canada), show large variability in ?13C (? 28.4 ‰ to ? 1.1‰, mode at ? 5.8‰), ?15N (? 5.8 to + 18.8‰, mode at ? 3.0‰) and nitrogen contents ([N]; 3800 to less than 1 at.ppm). In combination, cathodoluminescence imaging and microbeam analyses reveal that the diamonds grew from multiple fluid pulses, with at least one major hiatus documented in some samples that was associated with a resorption event and an abrupt change from low ?13C and [N] to mantle-like ?13C and high [N]. Overall, ?13C appears to be uncorrelated to ?15N and [N] on both the inter- and intra-diamond levels. Co-variations of ?15N-log[N], however, result in at least two parallel, negatively correlated linear arrays, which are also present on the level of the individual diamonds falling on these two trends. These arrays emerge from the two principal data clusters, are characterized by slightly negative and slightly positive ?15N (about ? 3 and + 2‰, respectively) and variable but overall high [N]. Using published values for the diamond-fluid nitrogen isotope fractionation factor and nitrogen partition coefficient, these trends are perfectly reproduced by a Rayleigh fractionation model. Overall, three key elements are identified in the formation of the diamond suite studied: (1.) a low ?13C and low [N] component that possibly is directly associated with an eclogitic diamond substrate or introduced during an early stage fluid event. (2.) Repeated influx of a variably nitrogen-rich mantle fluid (mildly negative ?13C and ?15N). (3.) In waning stages of influx, availability of the mantle-type fluid at the site of diamond growth became limited, leading to Rayleigh fractionation. These fractionation trends are clearly depicted by ?15N-[N] but are not detected when examining co-variation diagrams involving ?13C. Also on the level of individual diamonds, large (? 5‰) variations in ?15N are associated with ?13C values that typically are constant within analytical uncertainty. The much smaller isotope fractionation factor for carbon (considering carbonate- or methane-rich fluids as possible carbon sources) compared to nitrogen leads to an approximately one order of magnitude lower sensitivity of ?13C values to Rayleigh fractionation processes (i.e. during fractionation, a 1‰ change in ?13C is associated with a 10‰ change in ?15N). As a consequence, even minor heterogeneity in the primary isotopic composition of diamond forming carbon (e.g., due to addition of minor subducted carbon) will completely blur any possible co-variations with ?15N or [N]. We suggest this strong difference in isotope effects for C and N to be the likely cause of observations of an apparently decoupled behaviour of carbon and nitrogen isotopes in diamond.
Abstract: Magnesium and oxygen are critical elements in the solid Earth and hydrosphere. A better understanding of the combined behavior of Mg and O isotopes will refine their use as a tracer of geochemical processes and Earth evolution. In this study, the Mg-isotope compositions of garnet and omphacite separated from well-characterized xenolithic eclogites from the Roberts Victor kimberlite pipe (South Africa) have been measured by solution multi-collector ICP-MS. The reconstructed whole-rock ?26Mg values of Type I (metasomatized) eclogites range from ? 0.61‰ to ? 0.20‰ (Type IA) and from ? 0.60‰ to ? 0.30‰ (Type IB) (mean ? 0.43‰ ± 0.12‰), while ?26Mg of Type IIA (fresh, least metasomatized) eclogites ranges from ? 1.09‰ to ? 0.17‰ (mean ? 0.69‰ ± 0.41‰); a Type IIB (fresh, least metasomatized) has ?26Mg of ? 0.37‰. Oxygen-isotope compositions of garnet were analyzed in situ by SIMS (CAMECA 1280) and cross-checked by laser fluorination. Garnets have ?18O of 6.53‰ to 9.08‰ in Type IA, 6.14‰ to 6.65‰ in Type IB, and 2.34‰ to 2.91‰ in Type IIB. The variation of ?26Mg and ?18O in Type IA and IB eclogites is consistent with the previously proposed model for the evolution of these samples, based on major and trace elements and radiogenic isotopes. In this model, the protoliths (Type II eclogites) were metasomatized by carbonatitic to kimberlitic melts/fluids to produce first Type IA eclogites and then Type IB. Metasomatism has changed the O-isotope compositions, but the Mg-isotope compositions of Type IA are mainly controlled by the protoliths; those of Type IB eclogites reflect mixing between the protoliths and the kimberlitic melt/fluid. The combination of a large range of ?26Mg and low ?18O in Type II eclogites cannot be explained easily by seawater alteration of oceanic crust, interaction of carbonate/silicate sediments with oceanic crust, or partial melting of mafic rocks.
Abstract: Alluvial diamonds from the Kasai River, Democratic Republic of the Congo (DRC) are sourced from Cretaceous kimberlites of the Lucapa graben in Angola. Analysis of 40 inclusion-bearing diamonds provides new insights into the characteristics and evolution of ancient lithospheric mantle of the Congo craton. Silicate inclusions permitted us to classify diamonds as peridotitic, containing Fo91-95 and En92-94, (23 diamonds, 70% of the suite), and eclogitic, containing Cr-poor pyrope and omphacite with 11-27% jadeite (6 diamonds, 18% of the suite). Fluid inclusion compositions of fibrous diamonds are moderately to highly silicic, matching compositions of diamond-forming fluids from other DRC diamonds. Regional homogeneity of Congo fibrous diamond fluid inclusion compositions suggests spatially extensive homogenization of Cretaceous diamond forming fluids within the Congo lithospheric mantle. In situ cathodoluminescence, secondary ion mass spectrometry and Fourier transform infrared spectroscopy reveal large heterogeneities in N, N aggregation into B-centers (NB), and ?13C, indicating that diamonds grew episodically from fluids of distinct sources. Peridotitic diamonds contain up to 2962 ppm N, show 0-88% NB, and have ?13C isotopic compositions from ? 12.5‰ to ? 1.9‰ with a mode near mantle-like values. Eclogitic diamonds contain 14-1432 ppm N, NB spanning 29%-68%, and wider and lighter ?13C isotopic compositions of ? 17.8‰ to ? 3.4‰. Fibrous diamonds on average contain more N (up to 2976 ppm) and are restricted in ?13C from ? 4.1‰ to ? 9.4‰. Clinopyroxene-garnet thermobarometry suggests diamond formation at 1350-1375 °C at 5.8 to 6.3 GPa, whereas N aggregation thermometry yields diamond residence temperatures between 1000 and 1280 °C, if the assumed mantle residence time is 0.9-3.3 Ga. Integrated geothermobaromtery indicates heat fluxes of 41-44 mW/m2 during diamond formation and a lithosphere-asthenosphere boundary (LAB) at 190-210 km. The hotter-than-average cratonic mantle may be attributable to contemporaneous rifting of the southern Atlantic, multiple post-Archean reactivations of the craton, and/or proximal Cretaceous plumes.
Abstract: Mineralogical studies and U-Pb dating have been carried out on rutile included in peridotitic and eclogitic garnets from the Internatsionalnaya pipe, Mirny field, Siberian craton. We also describe a unique peridotitic paragenesis (rutile + forsterite + enstatite + Cr-diopside + Cr-pyrope) preserved in diamond from the Mir pipe, Mirny field. Compositions of rutile from the heavy mineral concentrates of the Internatsionalnaya pipe and rutile inclusions in crustal almandine-rich garnets from the Mayskaya pipe (Nakyn field), as well as from a range of different lithologies, are presented for comparison. Rutile from cratonic mantle peridotites shows characteristic enrichment in Cr, in contrast to lower-Cr rutile from crustal rocks and off-craton mantle. Rutile with Cr2O3 > 1.7 wt% is commonly derived from cratonic mantle, while rutiles with lower Cr2O3 may be both of cratonic and off-cratonic origin. New analytical developments and availability of standards have made rutile accessible to in situ U-Pb dating by laser ablation ICP-MS. A U-Pb age of 369 ± 10 Ma for 9 rutile grains in 7 garnets from the Internatsionalnaya pipe is consistent with the accepted eruption age of the pipe (360 Ma). The equilibrium temperatures of pyropes with rutile inclusions calculated using Ni-in-Gar thermometer range between ~ 725 and 1030 °C, corresponding to a depth range of ca ~ 100-165 km. At the time of entrainment in the kimberlite, garnets with Cr-rich rutile inclusions resided at temperatures well above the closure temperature for Pb in rutile, and thus U-Pb ages on mantle-derived rutile most likely record the emplacement age of the kimberlites. The synthesis of distinctive rutile compositions and U-Pb dating opens new perspectives for using rutile in diamond exploration in cratonic areas.
Abstract: A xenolith of eclogite from the kimberlite pipe Udachnaya-East, Yakutia Grt+Cpx+Ky + S + Coe/Qtz + Dia + Gr has been studied. Graphite inclusions in diamond have been studied in detail by Confocal Raman (CR) mapping. The graphite inclusion in diamond has a highly ordered structure and is characterized by a substantial shift in the band (about 1580 cm-1) by 7 cm-1, indicating a significant residual strain in the inclusion. According to the results of FTIR spectroscopic studies of diamond crystals, a high degree of nitrogen aggregation has been detected: it is present mainly in form A, which means an "ancient" age of the diamonds. In the xenolith studied, the diamond formation occurred about 1 Byr, long before their transport by the kimberlite melt, and the conditions of the final equilibrium were temperatures of 1020 ± 40°C at 4.7 GPa. Thus, these graphite inclusions found in a diamond are the first evidence of crystallization of metastable graphite in a diamond stability field. They were formed in rocks of the upper mantle significantly below (?20 km) the graphite-diamond equilibrium line.
Abstract: Fe-rich carbonatites with a mineral assemblage of ankerite-calcite or siderite are widespread in southern Siberia, Russia. The siderite carbonatites are associated with F-Ba-Sr-REE mineralization and have a 40Ar/39Ar age of 117.2 ± 1.3 Ma. Melt and fluid inclusions suggest that the carbonatites formed from volatile-rich alkali- and chloride-bearing carbonate melts. Ankerite-calcite carbonatites formed from carbonatite melt at a temperature of more than 790 °C. The ferrocarbonatites (the second phase of carbonatite intrusion) formed from a sulfate-carbonate-chloride fluid phase (brine-melt) at >650 °C and ?360 MPa. The brine-melt fluid phase had high concentrations of Fe and LREEs. A subsequent hydrothermal overprint contributed to the formation of economically important barite-Sr-fluorite-REE mineralization in polymict siderite breccia.
Abstract: Type Ib diamonds contain abundant isolated nitrogen and account for less than 0.1% of natural diamonds. This rarity is because over geological time and at temperatures typical of the cratonic lithosphere, isolated nitrogen aggregates to A centres (N pairs) and B centres (4N around a vacancy). Preservation of isolated nitrogen in natural diamonds requires either short mantle residency times or storage at temperatures <700 °C, whereas most cratonic diamonds are billions of years old and resided >1000 °C. Eclogitic sulphides in Zimmi Ib diamonds (Sierra Leone) have 650 Ma Re-Os ages, whose origin is best explained by rapid tectonic exhumation after continental collision to shallower depths in the keel prior to kimberlite eruption (Smit et al., 2016). Here we present SIMS and spectroscopic data for a new suite of Zimmi sulphide-bearing diamonds. These new data allow us to evaluate the speciation of diamond source fluids, and the defects in these diamonds that are responsible for their distinctive canary yellow colours. The combined dataset establishes the link between the spectroscopic features in Zimmi Ib diamonds and their unusual history. Low ?13C values below -15 ‰ in 3 diamonds result from source fluids that originated as organic carbon in the oceanic crust, and were recycled into the lithosphere during subduction. In particular, a trend of decreasing ?13C and N content from core to rim in a single diamond indicates closed-system growth from CH4-rich subducted fluids. Recycled origins for organic carbon supports the temporal link of Zimmi diamond formation with deep underthrusting during Neoproterozoic continental assembly, recorded in the Rokelide orogen. CL imaging of Zimmi diamonds reveals irregular growth patterns with abundant deformation lines, associated with tectonic exhumation of the diamonds. Vacancies formed by deformation were subsequently annealed to form NV centres, where the negative charge state (637 nm) is more abundant due to isolated nitrogen donating an electron. Fancy brownish-yellow to greenish-yellow colours observed in Zimmi Ib diamonds result from a combination of isolated nitrogen, deformation-related amber centres and NV centres. These colour-forming defects can all be attributed to the unique geological history of Zimmi Ib diamonds and their rapid exhumation after formation.
Abstract: Polycrystalline diamond aggregates (boart, framesites, diamondites) have been widely studied but their origin is poorly understood. We report the results of a study in situ of two polished fragments of fine-grained (40-400 ?m size of individual diamond grains) dense polycrystalline diamond aggregates from the Mir pipe containing visible multiple interstitial garnet inclusions. They were analyzed for major and trace elements of inclusions and one of them — for ?13C and N abundance and isotopic composition of host diamonds. These aggregates are classified as variety IX by Orlov (1977). No cavities were observed in these samples. Sixty two irregular garnet grains and one clinopyroxene inclusion were detected and analyzed in sample Mr 832. Garnets are homogeneous within single grains but variable in Mg# [100Mg/(Mg + Fe)] from 60 up to 87 and CaO contents (3.3-5.3 wt.%) among grains with a trend to negative correlation. Low Cr (550-640 ppm) confirms eclogitic (E-type) paragenesis. High Na2O contents (5.2 wt.%) of a single pyroxene inclusion are additional evidence of eclogitic nature of this sample. Wide variations in trace elements (ppm) are characteristic for garnet grains: Sr (2.7-25.6), Y (9.7-14.1), Zr (15.6-38.7) and positive Eu anomaly is present. The ?13C of diamonds within studied sample is variable (? 6.4 ÷? 9.8 ‰) as well as N abundance (75-1150 ppm) and ?15N ? 27, ? 38, ? 58 ‰. The second peridotitic (U/P-type) sample Mr 838 contains eight inclusions of Mg-rich Cr-pyropes (Mg# ~ 85, Cr2O3 3.2-3.4 wt.%) and magnesite inclusion with 4.35 wt.% FeO and 1.73 wt.% CaO. Trace element content in pyropes is relatively uniform (ppm): Sr (0.4-1.6), Y (13.2-13.4) and Zr (13.0). We conclude that heterogeneous distribution of the trace elements among garnet grains in Mr 832 and magnesite presence in Mr 838 are indicative of the effects of mantle metasomatism and rapid crystallization shortly before the eruption of the kimberlite.
Abstract: Homogeneity of a peridotitic garnet inclusion in diamond demonstrating excess in Si concentration (i.e. presence of majorite component) was investigated by TEM using FIB prepared foils. The host diamond is a low-nitrogen brown stone, which can be related to type IIa with features of strong plastic deformation. The studied sample is represented by Ca-poor Cr-pyrope of harzburgitic (H) paragenesis from Snap Lake dyke, Canada The garnet had been previously reported to contain Si = 3.16 apfu. The revised examination of the sample, resulted in detection of extremely fine-grained symplectite consisting of low Ca-orthopyroxene, clinopyroxene, Cr-spinel and coesite completely located and isolated in the inner part of the garnet crystal, which forms a sharp interface with the surrounding homogeneous garnet. XRD study confirmed the presence of the minerals constituting the symplectite. EPMA showed an identical bulk chemistry of the nanometer-sized symplectite and garnet. Further polishing of the garnet inclusion on the same surface with diamond removed the symplectite, which possibly was present as a thin lens within garnet. The remaining garnet is completely homogeneous as checked by two profiles, and contains unusually high Ni (118.2 ppm) and depleted REE patterns. Estimated PT formation conditions of this garnet are 10.8 GPa and 1450 °C within asthenosphere. Symplectite testifies partial retrograde isochemical phase transformation of the examined garnet which is suggested to be caused by decompression along with plastic deformation of diamond within the coesite stability field at T > 1000 °C and depth no less than 100 km. Because previously published studies of rare majoritic garnets composition were performed by EPMA only, it is possible that the traces of partial phase transformation (symplectite formation) could have been overlooked without additional XRD and/or TEM/AEM studies.
Abstract: The trace element compositions of inclusions in sub-lithospheric diamonds from the Juina-5 kimberlite, Brazil, are presented. Literature data for mineral/melt partition coefficients were collated, refitted and employed to interpret inclusion compositions. As part of this process an updated empirical model for predicting the partitioning behaviour of trivalent cations for garnet-melt equilibrium calibrated using data from 73 garnet-melt pairs is presented. High levels of trace element enrichment in inclusions interpreted as former calcium silicate perovskite and majoritic garnet preclude their origin as fragments of an ambient deep mantle assemblage. Inclusions believed to represent former bridgmanite minerals also display a modest degree of enrichment relative to mantle phases. The trace element compositions of ‘NAL’ and ‘CF phase’ minerals are also reported. Negative Eu, Ce, and Y/Ho anomalies alongside depletions of Sr, Hf and Zr in many inclusions are suggestive of formation from a low-degree carbonatitic melt of subducted oceanic crust. Observed enrichments in garnet and ‘calcium perovskite’ inclusions limit depths of melting to less than ~ 600 km, prior to calcium perovskite saturation in subducting assemblages. Less enriched inclusions in sub-lithospheric diamonds from other global localities may represent deeper diamond formation. Modelled source rock compositions that are capable of producing melts in equilibrium with Juina-5 ‘calcium perovskite’ and majorite inclusions are consistent with subducted MORB. Global majorite inclusion compositions suggest a common process is responsible for the formation of many superdeep diamonds, irrespective of geographic locality. Global transition zone inclusion compositions are reproduced by fractional crystallisation from a single parent melt, suggesting that they record the crystallisation sequence and melt evolution during this interaction of slab melts with ambient mantle. All observations are consistent with the previous hypothesis that many superdeep diamonds are created as slab-derived carbonatites interact with peridotitic mantle in the transition zone.
Abstract: "Super-deep" diamonds are thought to crystallize between 300 and 800 km depth because some of the inclusions trapped within them are considered to be the products of retrograde transformation from lower mantle or transition zone precursors. In particular, single inclusion CaSiO3-walstromite is believed to derive from CaSiO3-perovskite, although its real depth of origin has never been proven. Our aim is therefore to determine for the first time the pressure of formation of the diamond-CaSiO3-walstromite pair by “single-inclusion elastic barometry” and to determine whether CaSiO3-walstromite derives from CaSiO3-perovskite or not. We investigated several single phases and assemblages of Ca-silicate inclusions still trapped in a diamond coming from Juina (Brazil) by in-situ analyses (single-crystal X-ray diffraction and micro-Raman spectroscopy) and we obtained a minimum entrapment pressure of ~ 5.7 GPa (? 180 km) at 1500 K. However, the observed coexistence of CaSiO3-walstromite, larnite (?-Ca2SiO4) and CaSi2O5-titanite in one multiphase inclusion within the same diamond indicates that the sample investigated is sub-lithospheric with entrapment pressure between ~ 9.5 and ~ 11.5 GPa at 1500 K, based on experimentally-determined phase equilibria. In addition, thermodynamic calculations suggested that, within a diamond, single inclusions of CaSiO3-walstromite cannot derive from CaSiO3-perovskite, unless the diamond around the inclusion expands by ~ 30% in volume.
Devriese, S.G.R., Corcoran, N., Cowan, D., Davis, K., Bild-Enkin, D., Fournier, D., Heagy, L., Kang, S., Marchant, D., McMillan, M.S., Mitchell, M., Rosenkjar, G., Yang, D., Oldenburg, D.W.
Abstract: The magnetic and electromagnetic responses from airborne systems at Tli Kwi Cho, a kimberlite complex in the Northwest Territories, Canada, have received considerable attention over the last two decades but a complete understanding of the causative physical properties is not yet at hand. Our analysis is distributed among three papers. In the first, we find a 3D magnetic susceptibility model for the area; in the second, we find a 3D conductivity model; and in the third paper, we find a 3D chargeability model. Our goal is to explain all the geophysical results within a geologic framework. In this first paper, we invert three independent airborne magnetic data sets flown over the Tli Kwi Cho kimberlite complex located in the Lac de Gras kimberlite field in Northwest Territories, Canada. The complex consists of two kimberlites known as DO-27 and DO- 18. An initial airborne DIGHEM survey was flown in 1992 and AeroTEM and VTEM data subsequently acquired in 2003 and 2004, respectively. In this paper, we invert each magnetic data set in three dimensions. Both kimberlites are recovered in each model, with DO-27 as a more susceptible body than DO-18. Our goal is to simultaneously invert the three data sets to generate a single susceptibility model for Tli Kwi Cho. This project is part of a larger, on-going investigation by UBC-GIF on inverting magnetic, electromagnetic, and induced polarization data from the Tli Kwi Cho area.
Fournier, D., Heagy, L., Corcoran, N., Cowan, D., Devriese, S.G.R., Bild-Enkin, D., Davis, K., Marchant, M., McMillan, M.S., Mitchell, M., Rosenkjar, G., Yang, D., Oldenburg, D.W.
Abstract: The magnetic and electromagnetic responses from airborne systems at Tli Kwi Cho, a kimberlite complex in the Northwest Territories, Canada, have received considerable attention over the last two decades but a complete understanding of the causative physical properties is not yet at hand. Our analysis is distributed among three posters. In the first we find a 3D magnetic susceptibility model for the area; in the second we find a 3D conductivity model; and in the third we find a 3D chargeability model that can explain the negative transient responses measured over the kimberlite pipes. In this second paper we focus upon the task of finding a conductivity model that is compatible with three airborne data sets flown between 1992 and 2004: one frequency-domain data set (DIGHEM) and two time-domain systems (AeroTEM and VTEM). The goal is to obtain a 3D model from which geologic questions can be answered, but even more importantly, to provide a background conductivity needed to complete the 3D IP inversion of airborne EM data. We begin by modifying our pre-existing 1D frequency and time domain inversion codes to produce models that have more lateral continuity. The results are useful in their own right but we have also found that 1D analysis is often very effective in bringing to light erroneous data, assisting in estimating noise floors, and providing some starting information for developing a background model for the 3D EM inversion. Here we show some results from our Laterally Constrained Inversion (LCI) framework. The recovered conductivity models seem to agree on the general location of the kimberlite pipes but disagree on the geometry and conductivity values at depth. The complete 3D inversions in time and frequency, needed to resolved these issues, are currently in progress.
Abstract: The petrogenesis of kimberlites commonly is obscured by interaction with hydrothermal fluids, including deuteric (late-magmatic) and/or groundwater components. To provide new constraints on the modification of kimberlite rocks during overprinting by such fluids and on the fractionation of kimberlite magmas during crystallisation, we have undertaken a detailed petrographic and geochemical study of a hypabyssal sample (BK) from the Bultfontein kimberlite (Kimberley, South Africa).
Geochemistry International, Vol. 54, 10, pp. 834-838.
South America, Brazil
Deposit - Sao Luiz
Abstract: We report cloudy micro- and nano-inclusions in a superdeep diamond from São-Luiz, Brazil which contains inclusions of ferropericlase (Mg, Fe)O and former bridgmanite (Mg, Fe)SiO3 and ringwoodite (Mg, Fe)2SiO4. Field emission-SEM and TEM observations showed that the cloudy inclusions were composed of euhedral micro-inclusions with grain sizes ranging from tens nanometers to submicrometers. Infrared absorption spectra of the cloudy inclusions showed that water, carbonate, and silicates were not major components of these micro- and nano-inclusions and suggested that the main constituent of the inclusions was infrared-inactive. Some inclusions were suggested to contain material with lower atomic numbers than that of carbon. Mineral phase of nano- and micro-inclusions is unclear at present. Microbeam X-ray fluorescence analysis clarified that the micro-inclusions contained transition metals (Cr, Mn, Fe, Co, Ni, Cu, Zn) possibly as metallic or sulfide phases. The cloudy inclusions provide an important information on the growth environment of superdeep diamonds in the transition zone or the lower mantle.
ASEG-PESA-AIG 2016 25th Geophysical Conference, 4p. Pdf
Canada, Northwest Territories
Deposit - Tli Kwi Cho
Abstract: In this study, we revisit three airborne EM surveys over Tli Kwi Cho (TKC). These consist of a frequency domain DIGHEM data set, and two time domain surveys, VTEM and AeroTEM. Negative transients have been recorded in both of the time domain surveys and we interpret these as arising from chargeable bodies. The kimberlite pipes are referred to as DO-27 and DO-18. We look in more detail at the transient data and apply the ATEM-IP inversion procedure to recover a 3D pseudo-chargeability distribution. Important components of the analysis involve estimating a background conductivity for the region. For DO-27 we have used a 3D parametric inversion to recover the conductivity from TEM data. The IP signal for the inversion is obtained by subtracting the time domain responses estimated by EM inversion from the observed background signal. This process also removes EM coupling noise that might be contaminating the data. The resultant IP data are inverted with a linear inverse approach using the sensitivity from the background conductivity. This yields a 3D model of pseudo-chargeability.
Africa, Zimbabwe, Australia, South America, Brazil
Deposit - Murowa, Argyle, Machado River
Abstract: Fourier Transform Infrared (FTIR) spectroscopy is a commonly-used technique for investigating diamonds, that gives the most useful information if spatially-resolved measurements are used. In this paper we discuss the best way to acquire and present FTIR data from diamonds, using examples from Murowa (Zimbabwe), Argyle (Australia) and Machado River (Brazil). Examples of FTIR core-to-rim line scans, maps with high spatial resolution and maps with high spectral resolution that are fitted to extract the spatial variation of different nitrogen and hydrogen defects are presented. Model mantle residence temperatures are calculated from the concentration of A and B nitrogen-containing defects in the diamonds using known times of annealing in the mantle. A new, two-stage thermal annealing model is presented that better constrains the thermal history of the diamond and that of the mantle lithosphere in which the diamond resided. The effect of heterogeneity within the analysed FTIR volume is quantitatively assessed and errors in model temperatures that can be introduced by studying whole diamonds instead of thin plates are discussed. The spatial distribution of VN3H hydrogen defects associated with the 3107 cm? 1 vibration does not follow the same pattern as nitrogen defects, and an enrichment of VN3H hydrogen at the boundary between pre-existing diamond and diamond overgrowths is observed. There are several possible explanations for this observation including a change in chemical composition of diamond forming fluid during growth or kinetically controlled uptake of hydrogen.
Africa, Zimbabwe, Australia, South America, Brazil
Deposit - Murowa, Argyle, Machado River
Abstract: Fourier Transform Infrared (FTIR) spectroscopy is a commonly-used technique for investigating diamonds, that gives the most useful information if spatially-resolved measurements are used. In this paper we discuss the best way to acquire and present FTIR data from diamonds, using examples from Murowa (Zimbabwe), Argyle (Australia) and Machado River (Brazil). Examples of FTIR core-to-rim line scans, maps with high spatial resolution and maps with high spectral resolution that are fitted to extract the spatial variation of different nitrogen and hydrogen defects are presented. Model mantle residence temperatures are calculated from the concentration of A and B nitrogen-containing defects in the diamonds using known times of annealing in the mantle. A new, two-stage thermal annealing model is presented that better constrains the thermal history of the diamond and that of the mantle lithosphere in which the diamond resided. The effect of heterogeneity within the analysed FTIR volume is quantitatively assessed and errors in model temperatures that can be introduced by studying whole diamonds instead of thin plates are discussed. The spatial distribution of VN3H hydrogen defects associated with the 3107 cm? 1 vibration does not follow the same pattern as nitrogen defects, and an enrichment of VN3H hydrogen at the boundary between pre-existing diamond and diamond overgrowths is observed. There are several possible explanations for this observation including a change in chemical composition of diamond forming fluid during growth or kinetically controlled uptake of hydrogen.
Abstract: Relations of graphite and diamond have been studied in a garnet-kyanite-clinopyroxene+sulfide+coesite/quartz+diamond+graphite eclogite xenolith from the Udachnaya-East kimberlite pipe in the Yakutian diamond province. Euhedral crystals of diamond and graphite occur in the intra- and intergranular space. The equilibrium conditions of diamond formation reconstructed by geothermobarometry for the Grt-Cpx-Ky-Coe mineral assemblage are 1020 ± 40 °C and 4.7 GPa. Raman imaging of graphite enclosed in diamond shows high ordering and a 9 cm?1 shift of the ~1580 cm?1 band. This Raman shift of graphite, as well as a 5 cm?1 shift of the 1332 cm?1 band of diamond, indicate large residual stress in graphite and in diamond around the inclusion, respectively. According to FTIR spectroscopy, nitrogen in diamond is highly aggregated and exists mainly as the A centers, while no other phases occur near graphite inclusions. Therefore, diamond in the analyzed eclogite sample must be quite old: it likely had crystallized long (~1 Byr) before it became entrained with kimberlite melt. New data show that graphite can stay in the upper mantle for billions of years without converting to diamond. Crystallization of various carbon polymorphs, both in laboratory and natural systems, remains poorly constrained. Graphite present in mantle and UHP rocks may be a metastable phase crystallized in the diamond stability field. This fact should be taken into consideration when deducing petrological constrains and distinguishing diamond and graphite subfacies in upper mantle.
Canadian Journal of Earth Sciences, Vol. 53, 1, pp. 41-58.
Canada, Northwest Territories
Deposit - Muskox
Abstract: We present petrography, mineralogy, and thermobarometry for 53 mantle-derived xenoliths from the Muskox kimberlite pipe in the northern Slave craton. The xenolith suite includes 23% coarse peridotite, 9% porphyroclastic peridotite, 60% websterite, and 8% orthopyroxenite. Samples primarily comprise forsteritic olivine (Fo 89-94), enstatite (En 89-94), Cr-diopside, Cr-pyrope garnet, and chromite spinel. Coarse peridotites, porphyroclastic peridotites, and pyroxenites equilibrated at 650-1220 °C and 23-63 kbar (1 kbar = 100 MPa), 1200-1350 °C and 57-70 kbar, and 1030-1230 °C and 50-63 kbar, respectively. The Muskox xenoliths differ from xenoliths in the neighboring and contemporaneous Jericho kimberlite by their higher levels of depletion, the presence of a shallow zone of metasomatism in the spinel peridotite field, a higher proportion of pyroxenites at the base of the mantle column, higher Cr2O3 in all pyroxenite minerals, and weaker deformation in the Muskox mantle. We interpret these contrasts as representing small-scale heterogeneities in the bulk composition of the mantle, as well as the local effects of interaction between metasomatizing fluid and mantle wall rocks. We suggest that asthenosphere-derived pre-kimberlitic melts and fluids percolated less effectively through the less permeable Muskox mantle, resulting in lower degrees of hydrous weakening, strain, and fertilization of the peridotitic mantle. Fluids tended to concentrate and pool in the deep mantle, causing partial melting and formation of abundant pyroxenites.
Canadian Journal of Earth Sciences, Vol. 52, 1, pp. 51-67.
Canada, Alberta
Deposit - Buffalo Head Hills
Abstract: Ice flow of the last glaciation in the Buffalo Head Hills kimberlite field of northern Alberta is reconstructed from landform interpretations and clast orientations for the purpose of aiding kimberlite exploration in the region. The paucity of bedrock outcrop and the absence of preserved striae and other erosional ice-flow indicators on the soft Cretaceous marine sediments inhibit detailed interpretations on glacial flow chronology. Poorly developed bedrock drumlins on the Buffalo Head Hills and erosional ice-flow indicators preserved on the kimberlite outcrops indicate southwestward ice flow during the maximum extent of ice during the last glaciation. During the deglaciation of northern Alberta, later phases of ice flow were controlled by lobes of surging ice, which surged into proglacial lakes. West of the Buffalo Head Hills, the maximum phase of southwest flow was followed by southeastward ice movement of the Peace River ice lobe. Similarly, east of the Buffalo Head Hills, the maximum phase of ice flow was superceded by a south-southwest ice advance of the Wasbasca ice lobe.
Abstract: Oldoinyo Lengai is situated within the Gregory Rift Valley (northern Tanzania) and is the only active volcano erupting natrocarbonatite lava. This study investigates the texture and mineralogy of the June 1993 lava at Oldoinyo Lengai, and presents petrographic evidence of liquid immiscibility between silicate, carbonate, chloride, and fluoride melt phases. The 1993 lava is a porphyritic natrocarbonatite consisting of abundant phenocrysts of alkali carbonates, nyerereite and gregoryite, set in a quenched groundmass, composed of sodium carbonate, khanneshite, Na-sylvite and K-halite, and a calcium fluoride phase. Dispersed in the lava are silicate spheroids (< 2 mm) with a cryptocrystalline silicate mineral assemblage wrapped around a core mineral. We have identified several textural features preserved in the silicate spheroids, melt inclusions, and carbonatite groundmass that exhibit evidence of silicate-carbonate, carbonate-carbonate and carbonate-halide immiscibility. Rapid quenching of the lava facilitated the preservation of the end products of these liquid immiscibility processes within the groundmass. Textural evidence (at both macro- and micro-scales) indicates that the silicate, carbonate, chloride and fluoride phases of the lava unmixed at different stages of evolution in the magmatic system.
Tectonic significance and redox state of Paleoproterozoic eclogite and pyroxenite components in the Slave cratonic mantle lithosphere, Voyageur kimberlite, Arctic Canada.
Abstract: Diamonds from Dachine, French Guiana, are unique among worldwide diamond populations. The diamonds were transported to the surface in an unusual ultramafic extrusive magma with an affinity to boninite or komatiite, which was emplaced within an arc geological setting at ~ 2.2 Ga. Dachine diamonds have internal and external morphologies indicative of relatively rapid growth from carbon oversaturated fluids or melts, and exhibit internal features consistent with residence in a high-strain environment. On the basis of nitrogen (N) defects the diamonds are categorized as Type Ib-IaA. The unusually low aggregation state of N places severe constraints on the thermal history of the diamonds, effectively ruling out derivation in convecting mantle. The carbon and N isotopic compositions of Dachine diamonds are consistent with a sedimentary source of carbon, with the majority of diamonds having ?13C values < ? 25‰ and ?15N values > + 4‰. The primary carbon was presumably deposited on an early Proterozoic seafloor. Sulphide inclusions have low Ni and Cr and are comparable to lithospheric eclogitic-type sulphide inclusions. Three garnet and one clinopyroxene inclusion are also eclogitic in composition, and one garnet inclusion has a majorite component indicating an origin around 250 km depth. The silicate inclusions are highly depleted in many incompatible trace elements (e.g. LREE, Nb, Hf, Zr), and modelling indicates an eclogitic source lithology that contained a LREE-enriched trace phase such as epidote or allanite, and an HFSE-rich phase such as rutile. Four of the five inclusions are unusually enriched in Mn, as well as Ni and Co, and modelling indicates a protolith with the bulk composition of subducted normal MORB plus about 10% ferromanganese crust component. We suggest a model wherein Dachine diamonds precipitated from remobilized sedimentary carbon at the slab-mantle interface from liquids derived ultimately by deserpentinization of slab peridotite at depths of ~ 200 to 250 km. These fluids may also trigger melting in wedge peridotite, resulting in a volatile-rich ultramafic melt that transports the diamonds rapidly to the surface. The process of diamond formation and exhumation from the slab mantle interface likely occurred in a Paleoproterozoic subduction zone and over a very limited timespan, likely less than a million years.
Abstract: A new suite of 173 clinopyroxene grains from heavy-mineral concentrates of the diamondiferous Novinka kimberlite (Upper Muna field, Yakutia) has been analyzed for major and minor elements with an electron microprobe to perform a thermobarometric study and model the thermal structure of the Archean Upper Muna lithospheric mantle. Scrupulous evaluation of propagation of analytical uncertainties on pressure estimates revealed that (1) the single-clinopyroxene geobarometer can be very sensitive to analytical uncertainties for particular clinopyroxene compositions, and that (2) most clinopyroxenes from Novinka have compositions that are sensitive to analytical uncertainties, notwithstanding their apparent compositional suitability for single-clinopyroxene thermobarometry based on previously proposed application limits. A test on various mantle clinopyroxenes containing different proportions of the sensitive elements Cr, Na, and Al allowed us to identify clinopyroxene compositions that produce unacceptably high propagated errors and to define appropriate analytical conditions (i.e., higher beam currents and longer counting times for specific elements) that allow precise P-T estimates to be obtained for sensitive compositions. Based on the results of our analytical test, and taking into account the intrinsic limitations of the single-clinopyroxene thermobarometer, we have designed a new protocol for optimum thermobarometry, which uses partly revised compositional filters. The new protocol permits precise computation of the conductive paleogeotherm at Novinka with the single-clinopyroxene thermobarometer of Nimis and Taylor (2000). Thermal modeling of the resulting P-T estimates indicates a ~34 mW/m2 surface heat flow, a thermal lithosphere thickness of ~225 km, and an over 100 km thick “diamond window” beneath Novinka in the middle Paleozoic (344-361 Ma). We estimate that appropriate analytical conditions may extend the applicability of single-clinopyroxene thermobarometry to over 90% of clinopyroxene-bearing garnet peridotites and pyroxenites and to ~70% of chromian-diopside inclusions in diamonds. In all cases, application to clinopyroxenes with Cr/(Cr+Al)mol < 0.1 is not recommended. We confirm the tendency of the single-clinopyroxene barometer to progressively underestimate pressure at P > 4.5 GPa.
Abstract: Mineral data from Yakutian kimberlites allow reconstruction of the history of lithospheric mantle. Differences occur in compositions of mantle pyropes and clinopyroxenes from large kimberlite pipes in the Alakit and Daldyn fields. In the Alakit field, Cr-diopsides are alkaline, and Stykanskaya and some other pipes contain more sub-calcic pyropes and dunitic-type diamond inclusions, while in the Daldyn field harzburgitic pyropes are frequent. The eclogitic diamond inclusions in the Alakit field are sharply divided in types and conditions, while in the Daldyn field they show varying compositions and often continuous Pressure-Temperature (P-T) ranges with increasing Fe# with decreasing pressures. In Alakit, Cr-pargasites to richterites were found in all pipes, while in Daldyn, pargasites are rare Dalnyaya and Zarnitsa pipes. Cr-diopsides from the Alakit region show higher levels of light Rare Earth Elements (LREE) and stronger REE-slopes, and enrichment in light Rare Earth Elements (LREE), sometimes Th-U, and small troughs in Nb-Ta-Zr. In the Daldyn field, the High Field Strength Elements HFSE troughs are more common in clinopyroxenes with low REE abundances, while those from sheared and refertilized peridotites have smooth patterns. Garnets from Alakit show HREE minima, but those from Daldyn often have a trough at Y and high U and Pb. PTXfO2 diagrams from both regions show similarities, suggesting similar layering and structures. The degree of metasomatism is often higher for pipes which show dispersion in P-Fe# trends for garnets. In the mantle beneath Udachnaya and Aykhal, pipes show 6-7 linear arrays of P-Fe# in the lower part of the mantle section at 7.5-3.0 GPa, probably reflecting primary subduction horizons. Beneath the Sytykanskaya pipe, there are several horizons with opposite inclinations which reflect metasomatic processes. The high dispersion of the P-Fe# trend indicating widespread metasomatism is associated with decreased diamond grades. Possible explanation of the differences in mineralogy and geochemistry of the mantle sections may relate to their tectonic positions during growth of the lithospheric keel. Enrichment in volatiles and alkalis possibly corresponds to interaction with subduction-related fluids and melts in the craton margins. Incorporation of island arc peridotites from an eroded arc is a possible scenario.
Abstract: The Dalnyaya kimberlite pipe (Yakutia, Russia) contains mantle peridotite xenoliths (mostly lherzolites and harzburgites) that show both sheared porphyroclastic (deformed) and coarse granular textures, together with ilmenite and clinopyroxene megacrysts. Deformed peridotites contain high-temperature Fe-rich clinopyroxenes, sometimes associated with picroilmenites, which are products of interaction of the lithospheric mantle with protokimberlite related melts. The orthopyroxene-derived geotherm for the lithospheric mantle beneath Dalnyaya is stepped similar to that beneath the Udachnaya pipe. Coarse granular xenoliths fall on a geotherm of 35 mWm?2 whereas deformed varieties yield a 45 mWm?2 geotherm in the 2-7.5 GPa pressure interval. The chemistry of the constituent minerals including garnet, olivine and clinopyroxene shows trends of increasing Fe# (=Fe/(Fe + Mg)) with decreasing pressure. This may suggest that the interaction with fractionating protokimberlite melts occurred at different levels. Two major mantle lithologies are distinguished by the trace element patterns of their constituent minerals, determined by LA-ICP-MS. Orthopyroxenes, some clinopyroxenes and rare garnets are depleted in Ba, Sr, HFSE and MREE and represent relic lithospheric mantle. Re-fertilized garnet and clinopyroxene are more enriched. The distribution of trace elements between garnet and clinopyroxene shows that the garnets dissolved primary orthopyroxene and clinopyroxene. Later high temperature clinopyroxenes related to the protokimberlite melts partially dissolved these garnets. Olivines show decreases in Ni and increases in Al, Ca and Ti from Mg-rich varieties to the more Fe-rich, deformed and refertilized ones. Minerals showing higher Fe# (0.11-0.15) are found within intergrowths of low-Cr ilmenite-clinopyroxene-garnet related to the crystallization of protokimberlite melts in feeder channels. In P-f(O2) diagrams, garnets and Cr-rich clinopyroxenes indicate reduced conditions at the base of the lithosphere at ?5 log units below a FMQ buffer. However, Cr-poor clinopyroxenes, together with ilmenite and some Fe-Ca-rich garnets, demonstrate a more oxidized trend in the lower part of lithosphere at ?2 to 0 log units relative to FMQ. Clinopyroxenes from xenoliths in most cases show conditions transitional between those determined for garnets and megacrystalline Cr-poor suite. The relatively low diamond grade of Dalnyaya kimberlites is explained by a high degree of interaction with the oxidized protokimberlite melts, which is greater at the base of the lithosphere.
Abstract: The results of the study of diamonds with inclusions of high-pressure modification of SiO2 (coesite) by Raman spectroscopy are reported. It is established that the octahedral crystal from the Zapolyarnaya pipe is characterized by the highest residual pressure (2.7 ± 0.07 GPa). An intermediate value of this parameter (2.1 ± 0.07 GPa) was obtained for a crystal of transitional habit from the Maiskaya pipe. The minimal Raman shift was registered for coesite in diamond from the Komsomol’skaya-Magnitnaya pipe and provided a calculated residual pressure of 1.8 ± 0.03 GPa. The residual pressures for crystals from the placer deposits of the Kuoika and Bol’shaya Kuonamka rivers are 2.7 ± 0.07 and 3.1 ± 0.1 GPa, respectively. Octahedral crystals were formed in the mantle at a higher pressure than rhombododecahedral diamonds.
Abstract: The results of the study of diamonds with inclusions of high-pressure modification of SiO2 (coesite) by Raman spectroscopy are reported. It is established that the octahedral crystal from the Zapolyarnaya pipe is characterized by the highest residual pressure (2.7 ± 0.07 GPa). An intermediate value of this parameter (2.1 ± 0.07 GPa) was obtained for a crystal of transitional habit from the Maiskaya pipe. The minimal Raman shift was registered for coesite in diamond from the Komsomol’skaya-Magnitnaya pipe and provided a calculated residual pressure of 1.8 ± 0.03 GPa. The residual pressures for crystals from the placer deposits of the Kuoika and Bol’shaya Kuonamka rivers are 2.7 ± 0.07 and 3.1 ± 0.1 GPa, respectively. Octahedral crystals were formed in the mantle at a higher pressure than rhombododecahedral diamonds.
Journal of Structural Geology, Vol. 86, pp. 47-61.
Africa, South Africa
Deposit - Venetia
Abstract: The Beit Bridge Complex of the Central Zone (CZ) of the Limpopo Belt hosts the 519 ± 6 Ma Venetia kimberlite diatremes. Deformed shelf- or platform-type supracrustal sequences include the Mount Dowe, Malala Drift and Gumbu Groups, comprising quartzofeldspathic units, biotite-bearing gneiss, quartzite, metapelite, metacalcsilicate and ortho- and para-amphibolite. Previous studies define tectonometamorphic events at 3.3-3.1 Ga, 2.7-2.5 Ga and 2.04 Ga. Detailed structural mapping over 10 years highlights four deformation events at Venetia. Rules-based implicit 3D modelling in Leapfrog Geo provides an unprecedented insight into CZ ductile deformation and sheath folding. D1 juxtaposed gneisses against metasediments. D2 produced a pervasive axial planar foliation (S2) to isoclinal F2 folds. Sheared lithological contacts and S2 were refolded into regional, open, predominantly southward-verging, E-W trending F3 folds. Intrusion of a hornblendite protolith occurred at high angles to incipient S2. Constrictional-prolate D4 shows moderately NE-plunging azimuths defined by elongated hornblendite lenses, andalusite crystals in metapelite, crenulations in fuchsitic quartzite and sheath folding. D4 overlaps with a: 1) 2.03-2.01 Ga regional M3 metamorphic overprint; b) transpressional deformation at 2.2-1.9 Ga and c) 2.03 Ga transpressional, dextral shearing and thrusting around the CZ and d) formation of the Avoca, Bellavue and Baklykraal sheath folds and parallel lineations.
Acta Geologica Sinica, Vol. 90, July abstract p. 191.
India
Deposit - Lattavaram
Abstract: Utility of geochemistry in mineral exploration is known since more than half-a-century. In reconnaissance diamond exploration, regolith geochemistry is a well known tool worldwide and helps in distinguishing bedrock geology in hard rock terrains. More than 100 kimberlite pipes were discovered so far in the Eastern Dharwar Craton (EDC) of South India by various public and private organizations. Within the EDC, majority of diamondiferous pipe clusters occur in Anantapur District of Andhra Pradesh state in India. Lattavaram kimberlite cluster (LKC) is one among them in this district and four pipes in this cluster are reported to be diamondiferous along with two kimberlite bodies at Muligiripalli. The kimberlite pipes at Lattavaram occur in semi-circular shape whereas a kimberlite body exposed at Muligiripalli village occurs as a dyke within the granitoid country. The pipe 4 at Lattavaram exhibits conspicuous difference in the soil color and texture i.e., greenish color and mottled texture when compared with the reddish brown compact residual soils of granitic country rock. In the Indian context, soil regolith geochemistry is not a popular subject in search of kimberlites. It is observed that little or no literature is available on the utility of regolith geochemistry applied to kimberlite or diamond exploration in India. An attempt is made in this study, to demonstrate and understand the spatial surface geochemical signatures using residual soil geochemistry on known kimberlite pipes viz., 3 and 4 of LKC. Spatial and statistical analysis of trace and rare earth elements revealed that certain elements show predominance in the vicinity of the kimberlite pipes which can act as an exploration guide in distinguishing kimberlitic rocks within a granitoid country. These elements show distinct variation in their dispersion in the soil which can be attributed to basement lithology. It is observed that elements like Cr, Ni, Co, Cu, Nb, Zr, Ti, Ba and rare earth elements (REE) are significantly enriched in the mottled zone and calcretized duricrust relative to the country rock granitoids. A suite of trace elements comprising those associated with ultramafic rocks (Cr, Co & Ni) and felsic rocks (Nb, La, Sm and P) can readily distinguish the ultramafic/kimberlitic regolith from that derived from granitoid or felsic rocks which can be used as an exploration path finder.
Abstract: New mineralogical and bulk-rock geochemical data for the recently recognised Mesoproterozoic (ca. 1100 Ma) and late Cretaceous (ca. 90 Ma) kimberlites in the Timmasamudram cluster (TKC) of the Wajrakarur kimberlite field (WKF), Eastern Dharwar Craton, southern India, are presented. On the basis of groundmass mineral chemistry (phlogopite, spinel, perovskite and clinopyroxene), bulk-rock chemistry (SiO2, K2O, low TiO2, Ba/Nb and La/Sm), and perovskite Nd isotopic compositions, the TK-1 (macrocrystic variety) and TK-4 (microcrystic variety) kimberlites in this cluster are here classified as orangeites (i.e. Group II kimberlites), with geochemical characteristics that are very similar to orangeites previously described from the Bastar Craton in central India, as well as the Kaapvaal Craton in South Africa. The remaining kimberlites (e.g., TK-2, TK-3 and the TK-1 microcrystic variant), are more similar to other 1100 Ma, Group I-type kimberlites of the Eastern Dharwar Craton, as well as the typical Group I kimberlites of the Kaapvaal Craton. Through the application of geochemical modelling, based on published carbonated peridotite/melt trace element partition coefficients, we show that the generation of the TKC kimberlites and the orangeites results from low degrees of partial melting of a metasomatised, carbonated peridotite.
Doklady Earth Sciences, Vol. 470, 2, pp. 1023-1026.
Russia, Siberia
Deposit - Billyakh River placers
Abstract: The mineral chemistry and crystal morphology of kimberlite pyropes from the Billyakh River placer in the northeastern Siberian craton are characterised in terms of the placer history. The pyropes bear signatures of chemical weathering (dissolution), presumably in a Middle Paleozoic laterite profile, and therefore were originally hosted by Middle Paleozoic kimberlites. The broad occurrence of placer pyropes with lateritic dissolution signatures points to the presence of Middle Paleozoic diamond-bearing kimberlites in the study area.
Journal of Volcanology and Seismology, Vol. 10, 5, pp. 339-346.
Russia, Kola Peninsula, Archangel
Deposit- Lomonsov
Abstract: This paper presents results from a study of the Lomonosov volcanic pipe as derived from anomalies of the microseismic field. Microseismic sounding revealed that this volcanic pipe is a cone-shaped body with a small gradient of microseismic intensity motion (2 to 5 dB). Discontinuities generally show greater contrasts compared with the variations of microseismic motion in the pipe body. Comparison of the results of this microseismic sounding with other geological and geophysical data showed that the intensities of the micro-seismic field along lines that traversed the pipe reflect realistic structures of a kimberlite pipe and the host rocks. The method of microseismic sounding was used to reconstruct the deeper structure of the volcanic pipe and the host rocks down to depths greater than 2 km. We estimated the velocity contrast and the errors involved in the identification of vertical boundaries of the pipe. The volcanic pipe has a shape that is consistent with a nearly vertical source situated at a depth of a few hundred meters. This is hypothesized to be a typical occurrence for other diamond-bearing pipes as well.
Geological Society of London, Special Publication no. 446 on line available
Canada, Ontario, Attawapiskat
Deposit - Tango
Abstract: Extensive drilling of the Tango Extension kimberlite pipe resulted in the construction of an emplacement model that revealed the complex architecture of two amalgamated pipes: an older pipe, the Tango Extension Deep, which is cut along its northern margin by the smaller Tango Extension pipe. The resulting volcano forms a complex pipe-in-pipe structure called the Tango Extension Super Structure. The emplacement of the Tango Extension Super Structure sequence indicates prolonged hiatuses, which, similar to other volcanoes classified as monogenetic, puts the classical monogenetic and polygenetic definitions of maar-diatreme volcanoes to the test. Although the Tango Extension and Tango Extension Deep volcanoes could be characterized individually as monogenetic volcanoes, the Tango Extension Super Structure shows evidence of the occurrence of the significant hiatuses typical of polygenetic volcanoes. We suggest that hiatuses that are long enough to consolidate earlier tephra unambiguously differentiate polygenetic from monogenetic maar-diatreme volcanoes.
Journal of South African Institute of Mining and Metallurgy, Vol. 116, Aug. pp. 731-737.
Africa, Namibia
Deposit - marine placers
Abstract: Over the past 80 years, the Namibian diamondiferous marine placer has been studied extensively to develop solutions for mining and sampling challenges. The types of studies include the statistical modelling of the distributions of the stone counts per sample; investigating the relationship between geology and the grade distribution; assessing the quality potential of the entrapment of the available diamond pulse; using predetermined acceptability of barren samples (zero proportion (Zp) samples) to model distributions; optimal sample sizes; and more. During early-stage project evaluation it is more important to find out if a particular area is likely to be above a specific cut-off grade than to focus on sampling for the purpose of accurate resource estimation. Previous work using mixed Poisson and Sichel distributions to model the abundant onshore diamond data has been very successful in modelling the long-tailed nature of these linear beach deposits. The means of these distributions are, however, sensitive to extreme values. Technical and cost constraints prevent a similar scale of sample collection in an adjacent, geologically equivalent, submerged beach environment. A method not sensitive to extreme values is thus required to make early-stage assessments of the likelihood that the grade of a particular target is above a minimum cut-off grade. The Nachman model describes the functional relationship between the mean population density and proportion of barren patches ( Zp) in a patchy environment. A prerequisite for using the Nachman model is that the underlying data must be modelled using a negative binomial distribution (NBD). The case study data is from an analogous area adjacent to the exploration target and meets the NBD requirement. It is thus appropriate to apply the Nachman model. The Nachman model provides an opportunity to use the observed Zpto predict the mean grade for an area at the very early stage of an exploration project. In future, early-stage exploration data from a homogenous geological zone exhibiting characteristics of the Nachman model assumptions can thus be used to rank and target those areas that show potential to be above the minimum required grade cut-off for follow-up sampling and inclusion in the mine planning cycle.
Journal of South African Institute of Mining and Metallurgy, Vol. 116, July pp. 629-635.
Africa, Namibia
Deposit - marine placers
Abstract: During early-stage diamond exploration projects, hard data underpinning spatial continuity is often very limited. An extreme example of this is a submerged diamondiferous marine placer target area alongside a current onshore mining area in southwestern Namibia. Although an abundance of geological and grade data exists for the adjacent onshore mining area, the target area itself contains no such information. Despite this apparent abundance of data, it is extremely difficult to obtain a variogram (Prins and Jacob, 2014) for use in this study area. The use of traditional simulation techniques is further hindered by the fact that diamond entrapment within the highly gullied footwall is non-stationary. An alternative approach for creating a simulated virtual orebody (VOB) is thus required in order to enable the assessment of sampling strategies. This paper demonstrates how expert opinion is used to generate a composite probability map for diamond concentration using a greyscale hand-sketching technique. The probability map is subsequently calibrated and populated using the diamond distribution for different raised beaches obtained from analog data based on sample results adjacent to the target area. The resultant grade simulation is used to test different sample scenarios and is a first step towards determining an appropriate sampling strategy for the target area. The VOB is used to analyse and rank the efficiency of different sampling strategies for grade determination of submerged diamondiferous linear beach exploration targets.
Journal of South African Institute of Mining and Metallurgy, Vol. 116, Aug. pp. 745-753.
Africa, South Africa
Deposit - Cullinan
Abstract: In 2012, Cullinan Diamond Mine began an expansion programme with the shaft deepening and development of access to the C-Cut 1 block at approximately 839 m below surface. The expansion programme is funded by a combination of bank loans and retained operating profit generated by the mine. Continuous production during deepening of the No. 1 Shaft, which is the rock hoisting shaft, was therefore critical for sustainability and efficiency as well as overall funding of the project. The deepening method, support design and verification, as well as learning outcomes pertaining to the extension of the No. 1 Shaft underneath the existing operating shaft are summarized, with emphasis on the importance of gaining some understanding of the shaft's host rock mass.
Abstract: The paper reports detailed data on phlogopite from kimberlite of three facies types in the Arkhangelsk Diamondiferous Province (ADP): (i) massive magmatic kimberlite (Ermakovskaya-7 Pipe), (ii) transitional type between massive volcaniclastic and magmatic kimberlite (Grib Pipe), and (iii) volcanic kimberlite (Karpinskii-1 and Karpinskii-2 pipes). Kimberlite from the Ermakovskaya-7 Pipe contains only groundmass phlogopite. Kimberlite from the Grib Pipe contains a number of phlogopite populations: megacrysts, macrocrysts, matrix phlogopite, and this mineral in xenoliths. Phlogopite macrocrysts and matrix phlogopite define a single compositional trend reflecting the evolution of the kimberlite melt. The composition points of phlogopite from the xenoliths lie on a single crystallization trend, i.e., the mineral also crystallized from kimberlite melt, which likely actively metasomatized the host rocks from which the xenoliths were captured. Phlogopite from volcaniclastic kimberlite from the Karpinskii-1 and Karpinskii-2 pipes does not show either any clearly distinct petrographic setting or compositional differentiation. The kimberlite was dated by the Rb-Sr technique on phlogopite and additionally by the 40Ar/39Ar method. Because it is highly probable that phlogopite from all pipes crystallized from kimberlite melt, the crystallization age of the kimberlite can be defined as 376 ± 3 Ma for the Grib Pipe, 380 ± 2 Ma for the Karpinskii-1 pipe, 375 ± 2 Ma for the Karpinskii-2 Pipe, and 377 ± 0.4 Ma for the Ermakovskaya-7 Pipe. The age of the pipes coincides within the error and suggests that the melts of the pipes were emplaced almost simultaneously. Our geochronologic data on kimberlite emplacement in ADP lie within the range of 380 ± 2 to 375 ± Ma and coincide with most age values for Devonian alkaline-ultramafic complexes in the Kola Province: 379 ± 5 Ma; Arzamastsev and Wu, 2014). These data indicate that the kimberlite was formed during the early evolution of the Kola Province, when alkaline-ultramafic complexes (including those with carbonatite) were emplaced.
Abstract: The paper reports detailed data on phlogopite from kimberlite of three facies types in the Arkhangelsk Diamondiferous Province (ADP): (i) massive magmatic kimberlite (Ermakovskaya-7 Pipe), (ii) transitional type between massive volcaniclastic and magmatic kimberlite (Grib Pipe), and (iii) volcanic kimberlite (Karpinskii-1 and Karpinskii-2 pipes). Kimberlite from the Ermakovskaya-7 Pipe contains only groundmass phlogopite. Kimberlite from the Grib Pipe contains a number of phlogopite populations: megacrysts, macrocrysts, matrix phlogopite, and this mineral in xenoliths. Phlogopite macrocrysts and matrix phlogopite define a single compositional trend reflecting the evolution of the kimberlite melt. The composition points of phlogopite from the xenoliths lie on a single crystallization trend, i.e., the mineral also crystallized from kimberlite melt, which likely actively metasomatized the host rocks from which the xenoliths were captured. Phlogopite from volcaniclastic kimberlite from the Karpinskii-1 and Karpinskii-2 pipes does not show either any clearly distinct petrographic setting or compositional differentiation. The kimberlite was dated by the Rb-Sr technique on phlogopite and additionally by the 40Ar/39Ar method. Because it is highly probable that phlogopite from all pipes crystallized from kimberlite melt, the crystallization age of the kimberlite can be defined as 376 ± 3 Ma for the Grib Pipe, 380 ± 2 Ma for the Karpinskii-1 pipe, 375 ± 2 Ma for the Karpinskii-2 Pipe, and 377 ± 0.4 Ma for the Ermakovskaya-7 Pipe. The age of the pipes coincides within the error and suggests that the melts of the pipes were emplaced almost simultaneously. Our geochronologic data on kimberlite emplacement in ADP lie within the range of 380 ± 2 to 375 ± Ma and coincide with most age values for Devonian alkaline-ultramafic complexes in the Kola Province: 379 ± 5 Ma; Arzamastsev and Wu, 2014). These data indicate that the kimberlite was formed during the early evolution of the Kola Province, when alkaline-ultramafic complexes (including those with carbonatite) were emplaced.
Journal of South African Institute of Mining and Metallurgy, Vol. 116, Apr. pp. 343-348.
Africa, South Africa
Deposit - Cullinan
Abstract: Near-infrared (NIR) spectroscopy sorting technology is incorporated in an automated optical mineral sorter that can discriminate between materials using the differences in characteristics when exposed to near-infrared radiation. During September 2014 to April 2015, a pilot plant that utilized NIR technology to discriminate between kimberlite and waste materials was commissioned to determine the viability of including this technology in the diamond winning process flow sheet at Cullinan Diamond Mine. The plant was used to minimize the waste content in the size fraction -70+35 mm that reports to the crushing section and then to the dense media separation process. This paper describes the initial test work, conducted at Mintek, that led to the decision to conduct a pilot-scale study. The mineralogical characterization of the feed and product streams to establish the sorting criteria and the operational data obtained during the pilot plant campaign are described. The results indicated a good possibility of discriminating between the kimberlite and waste material using NIR technology. However, the consistency of discrimination was not good enough to avoid the risk of potential diamond loss. Furthermore, a lower than expected availability of the machine reduced the throughput capabilities.
Abstract: Mineralogical studies and U-Pb dating have been carried out on rutile included in peridotitic and eclogitic garnets from the Internatsionalnaya pipe, Mirny field, Siberian craton. We also describe a unique peridotitic paragenesis (rutile + forsterite + enstatite + Cr-diopside + Cr-pyrope) preserved in diamond from the Mir pipe, Mirny field. Compositions of rutile from the heavy mineral concentrates of the Internatsionalnaya pipe and rutile inclusions in crustal almandine-rich garnets from the Mayskaya pipe (Nakyn field), as well as from a range of different lithologies, are presented for comparison. Rutile from cratonic mantle peridotites shows characteristic enrichment in Cr, in contrast to lower-Cr rutile from crustal rocks and off-craton mantle. Rutile with Cr2O3 > 1.7 wt% is commonly derived from cratonic mantle, while rutiles with lower Cr2O3 may be both of cratonic and off-cratonic origin. New analytical developments and availability of standards have made rutile accessible to in situ U-Pb dating by laser ablation ICP-MS. A U-Pb age of 369 ± 10 Ma for 9 rutile grains in 6 garnets from the Internatsionalnaya pipe is consistent with the accepted eruption age of the pipe (360 Ma). The equilibrium temperatures of pyropes with rutile inclusions calculated using Ni-in-Gar thermometer range between ~ 725 and 1030 °C, corresponding to a depth range of ca ~ 100-165 km. At the time of entrainment in the kimberlite, garnets with Cr-rich rutile inclusions resided at temperatures well above the closure temperature for Pb in rutile, and thus U-Pb ages on mantle-derived rutile most likely record the emplacement age of the kimberlites. The synthesis of distinctive rutile compositions and U-Pb dating opens new perspectives for using rutile in diamond exploration in cratonic areas.
Doklady Earth Sciences, Vol. 470, 2, pp. 1059-1062.
Russia
Deposit - Internationalskaya
Abstract: The staged high-pressure annealing of natural cubic diamonds with numerous melt microinclusions from the Internatsional’naya kimberlite pipe was studied experimentally. The results mainly show that the carbonate phases, the daughter phases in partially crystallized microinclusions in diamonds, may undergo phase transformations under the mantle P-T conditions. Most likely, partial melting and further dissolution of dolomite in the carbonate-silicate melt (homogenization of inclusions) occur in inclusions. The experimental data on the staged high-pressure annealing of diamonds with melt microinclusions allow us to estimate the temperature of their homogenization as 1400-1500°C. Thus, cubic diamonds from the Internatsional’naya pipe could have been formed under quite high temperatures corresponding to the lithosphere/asthenosphere boundary. However, it should be noted that the effect of selective capture of inclusions with partial loss of volatiles in relation to the composition of the crystallization medium is not excluded during the growth. This may increase the temperature of their homogenization significantly between 1400 and 1500°C.
Journal of South African Institute of Mining and Metallurgy, Vol. 116, Feb. pp. 189-201.
Canada, Northwest Territories
Deposit - Fox, Ekati
Abstract: Multiple-point simulation (MPS) methods have been developed over the last decade as a means of reproducing complex geological patterns while generating stochastic simulations. Some geological spatial configurations are complex, such as the spatial geometries and patterns of diamond-bearing kimberlite pipes and their internal facies controlling diamond quality and distribution. Two MPS methods were tested for modelling the geology of a diamond pipe located at the Ekati mine, NT, Canada. These are the single normal equation simulation algorithm SNESIM, which captures different patterns from a training image (TI), and the filter simulation algorithm FILTERSIM, which classifies the patterns founded on the TI. Both methods were tested in the stochastic simulation of a four-category geology model: crater, diatreme, xenoliths, and host rock. Soft information about the location of host rock was also used. The validation of the simulation results shows a reasonable reproduction of the geometry and data proportions for all geological units considered; the validation of spatial statistics, however, shows that although simulated realizations from both methods reasonably reproduce the fourth-order spatial statistics of the TI, they do not reproduce well the same spatial statistics of the available data (when this differs from the TI). An interesting observation is that SNESIM better imitated the shape of the pipe, while FILTERSIM yielded a better reproduction of the xenolith bodies.
Journal of South African Institute of Mining and Metallurgy, Vol. 116, Feb. pp. 189-201.
Canada, Northwest Territories
Deposit - Fox, Ekati
Abstract: Multiple-point simulation (MPS) methods have been developed over the last decade as a means of reproducing complex geological patterns while generating stochastic simulations. Some geological spatial configurations are complex, such as the spatial geometries and patterns of diamond-bearing kimberlite pipes and their internal facies controlling diamond quality and distribution. Two MPS methods were tested for modelling the geology of a diamond pipe located at the Ekati mine, NT, Canada. These are the single normal equation simulation algorithm SNESIM, which captures different patterns from a training image (TI), and the filter simulation algorithm FILTERSIM, which classifies the patterns founded on the TI. Both methods were tested in the stochastic simulation of a four-category geology model: crater, diatreme, xenoliths, and host rock. Soft information about the location of host rock was also used. The validation of the simulation results shows a reasonable reproduction of the geometry and data proportions for all geological units considered; the validation of spatial statistics, however, shows that although simulated realizations from both methods reasonably reproduce the fourth-order spatial statistics of the TI, they do not reproduce well the same spatial statistics of the available data (when this differs from the TI). An interesting observation is that SNESIM better imitated the shape of the pipe, while FILTERSIM yielded a better reproduction of the xenolith bodies.
Abstract: This paper presents new major and trace element data from 150 garnet xenocrysts from the V. Grib kimberlite pipe located in the central part of the Arkhangelsk diamondiferous province (ADP). Based on the concentrations of Cr2O3, CaO, TiO2 and rare earth elements (REE) the garnets were divided into seven groups: (1) lherzolitic “depleted” garnets (“Lz 1”), (2) lherzolitic garnets with normal REE patterns (“Lz 2”), (3) lherzolitic garnets with weakly sinusoidal REE patterns (“Lz 3”), (4) lherzolitic garnets with strongly sinusoidal REE patterns (“Lz 4”), (5) harzburgitic garnets with sinusoidal REE patterns (“Hz”), (6) wehrlitic garnets with weakly sinusoidal REE patterns (“W”), (7) garnets of megacryst paragenesis with normal REE patterns (“Meg”). Detailed mineralogical and geochemical garnet studies and modeling results suggest several stages of mantle metasomatism influenced by carbonatite and silicate melts. Carbonatitic metasomatism at the first stage resulted in refertilization of the lithospheric mantle, which is evidenced by a nearly vertical CaO-Cr2O3 trend from harzburgitic (“Hz”) to lherzolitic (“Lz 4”) garnet composition. Harzburgitic garnets (“Hz”) have probably been formed by interactions between carbonatite melts and exsolved garnets in high-degree melt extraction residues. At the second stage of metasomatism, garnets with weakly sinusoidal REE patterns (“Lz 3”, “W”) were affected by a silicate melt possessing a REE composition similar to that of ADP alkaline mica-poor picrites. At the last stage, the garnets interacted with basaltic melts, which resulted in the decrease CaO-Cr2O3 trend of “Lz 2” garnet composition. Cr-poor garnets of megacryst paragenesis (“Meg”) could crystallize directly from the silicate melt which has a REE composition close to that of ADP alkaline mica-poor picrites. P-T estimates of the garnet xenocrysts indicate that the interval of ?60-110 km of the lithospheric mantle beneath the V. Grib pipe was predominantly affected by the silicate melts, whereas the lithospheric mantle deeper than 150 km was influenced by the carbonatite melts.
Abstract: Microinclusions of high-density fluids (HDF's) occur in cloudy diamonds from the Mir and Internatsionalnaya kimberlite pipes (Malobotuobia kimberlite field, Siberian platform). These HDFs are of typical high-Mg carbonatitic composition; a few diamonds contain microinclusions that define a low-Mg carbonatitic to silicic trend. The observed variations are interpreted as resulted from mixing of two contrasting fluids derived from the partial melting mainly of carbonated peridotite (the high-Mg carbonatitic HDFs) and eclogite (silica-rich HDFs and HDFs with high Ca/(Ca + Mg + Fe)). Immiscibility of carbonatitic and silica-rich fluids provides a possible mechanism for the co-existence of the observed HDFs but needs further proof. The uniform carbon isotope composition of cloudy diamonds with high-Mg carbonatitic microinclusions from both kimberlite pipes implies a single peridotitic source.
Smit, K.V., Shirey, S.B., Stern, R.A., Steele, A., Wang, W.
Diamond growth from C-H-N-O recycled fluids in the lithosphere: Evidence from CH4 micro-inclusions and dleta 13 C-Delta 15 N-N content in Marange mixed-habit diamonds.
Abstract: Neoproterozoic kimberlite, ultramafic lamprophyre, and carbonatite magmatic activity was widespread across the Canadian-Greenland Shield. Models to explain the preponderance of this deeply-derived CO2-rich magmatism between 680-540 Ma range from impingement of multiple mantle plumes to rifting activity linked to the breakout of the Laurentian plate from the Rodinia supercontinent configuration. We add to the debate about the origin of kimberlite magmas and evaluate possible mantle sources of the 655 Ma ‘diamond-rich’ Renard (new SIMS U/Pb perovskite ages) and 629 Ma ‘barren’ Wemindji kimberlites on the eastern Superior craton in Quebec, Canada. Our Sr-Nd-Hf and carbon isotope data (87Sr/86Sri = 0.70241-0.70442; ?Ndi = + 0.2 to + 4.8; ?Hfi = + 0.3 to + 6.5; ?13C = ? 5.6 to ? 3.9‰) suggest a common and moderately depleted convecting upper mantle source region for both the Renard and Wemindji kimberlites, which occur 400 km apart in the interior of the Superior craton. In contrast, the low Os isotope ratios (187Os/188Osi = 0.11078-0.12620; ?Osi = ? 13.7 to ? 1.6) and unfractionated chondritic relative HSE abundances (Os, Ir, Ru, Pt, Pd, Re) indicate significant involvement of ancient refractory cratonic mantle material in kimberlite magma formation. Our model calculations suggest that for both the diamond-rich Renard and the barren Wemindji kimberlite magmas up to 30% of the Os was derived from refractory cratonic peridotites. This material might have been assimilated by originally more CO2-rich carbonated silicate melts derived from the asthenosphere. We also show that the geochemical and Sr-Nd-Hf-Os isotopic compositions of the Renard and Wemindji kimberlites do not require significant input from melts derived from olivine-poor cratonic mantle lithologies such as MARID-type veins and pyroxenites/eclogites. This contrasts with the petrogenesis of deeply-derived volatile-rich potassic magmas found along the peripheries of cratons (e.g., ultramafic lamprophyres, kamafugites, and olivine lamproites), a setting where abundant non-peridotitic components have been added to the lithospheric mantle over the course of continent evolution. Provided that CO2-rich melts, such as proto-kimberlites, occur near the solidus of volatile-fluxed peridotites, no excess mantle heat is required in their formation. This important but often overlooked constraint, together with the observation that there exist no spatial or temporal relationships between the Superior craton kimberlites and Large Igneous Provinces during the Late Neoproterozoic, suggests that kimberlite magmatic activity was tectonically controlled. In our preferred model, ubiquitous CO2-rich proto-kimberlite melts form during volatile-controlled redox melting processes at ambient mantle temperatures in a thermal boundary layer directly beneath thick cratonic lithosphere. The success rate of ‘evolving’ hybrid kimberlite magmas reaching Earth’s surface increases when tensile stresses propagate into the > 200 km thick keels of continental lithosphere. These conditions are frequently met during fast and changing plate motions associated with the assembly and breakup of supercontinents.
Examination of diamond stability phase mantle indicator minerals from Leucite Hills, Sweetwater County, Wyoming and Crater of Diamonds State Park, Pike Count, Arkansas.
Geological Society of America, Vol. 48, 3, 1p. Abstract
Journal of Mining Science, Vol. 52, no. 2, pp. 332-340.
Russia, Yakutia
Deposit - Mir
Abstract: The article gives new experimental data on spectral characteristics of photoluminescence of natural diamonds extracted from deep horizons of Mir and Internatsionalnaya Pipes, Republic of Sakha (Yakutia) depending on composition of basic and additional optically active structural defects in crystals and on temperature during spectrum recording, considering kinetics of luminescence. It is hypothesized on applicability of low-temperature effects to enhance efficiency of photoluminescence separation of diamond crystals.
Doklady Earth Sciences, Vol. 471, 1, pp. 1104-1207.
Russia
Deposit - Udachnaya
Abstract: New results of Rb-Sr and Sm-Nd isotope analyses have been obtained on samples of deformed peridotite xenoliths collected from the Udachnaya kimberlite pipe (Yakutia). The data obtained imply two main stages of metasomatic alteration of the lithospheric mantle base matter in the central part of the Siberian Craton. Elevated ratios of Sr isotopes may be considered as evidence of an ancient stage of metasomatic enrichment by a carbonatite melt. The acquired Nd isotope composition together with the geochemistry of the deformed peridotite xenoliths suggests that the second stage of metasomatic alteration took place shortly before formation of the kimberlite melt. The metasomatic agent of this stage had a silicate character and arrived from an asthenosphere source, common for the normal OIB type (PREMA) and the Group-I kimberlite.
Abstract: Kimberlites are not only the most economically important source of diamonds; they also carry unique information encapsulated in rock fragments entrained as the magma traverses the whole thickness of the lithosphere. The Nurbinskaya pipe in the Siberian kimberlite province (Russia) is one of several intruded along the Vilyui Rift, a major terrane boundary. The pipe contains three populations of mantle-derived zircon xenocrysts: Archean (mean age 2709 ± 9 Ma), Devonian (mean age 371 ± 2.3 Ma), and a subset of grains with evidence of brittle deformation and rehealing, and a range of ages between 370 and 450 Ma. The Hf-isotope, O-isotope and trace-element signatures of the last group provide a link between the Archean and Devonian events, indicating at least three episodes of magmatic activity and zircon crystallization in the lithosphere beneath the pipe. The emplacement of the Nurbinskaya pipe ca 370 Ma ago was only the youngest activity in a magma plumbing system that has been periodically reactivated over at least 2.7 billion years, controlled by the lithosphere-scale structure of the Vilyui Rift.
Journal of African Earth Sciences, Vol. 126, pp. 33-44.
Africa, Tanzania
Deposit - Panda Hill
Abstract: The Mesozoic Panda Hill carbonatite deposit in western Tanzania hosts pyrochlore, an ore and source of niobium. This study was conducted to establish the contents of radioactive elements (uranium and thorium) in pyrochlore along with the concentration of niobium in the ore. The pyrochlore is mainly hosted in sövite and is structurally controlled by NW-SE (SW dipping) or NE-SW (NW dipping) magmatic flow bands with dip angles of between 60° and 90°. Higher concentrations of pyrochlore are associated with magnetite, apatite and/or phlogopite rich flow bands. Electron microprobe analyses on single crystals of pyrochlore yield very low UO2 concentrations that range between 0 and 0.09 wt% (equivalent to 0 atoms per formula unit: a.p.f.u.) and ThO2 between 0.55 and 1.05 wt% (equivalent to 0.1 a.p.f.u.). The analyses reveal high concentrations of Nb2O5 (ranging between 57.13 and 65.50 wt%, equivalent to a.p.f.u. ranging between 1.33 and 1.43) and therefore the Panda Hill Nb-oxide is classified as pyrochlore sensu stricto. These data point to a non radioactive pyrochlore and a deposit rich in Nb at Panda Hill. The Panda Hill pyrochlore has low concentrations of REEs as displayed by La2O3 that range between 0.10 and 0.49 wt% (equivalent to a.p.f.u. ranging between 0 and 0.01) and Ce2O3 ranging between 0.86 and 1.80 wt% (equivalent to a.p.f.u. ranging between 0.02 and 0.03), Pr2O3 concentrations range between 0 and 0.23 wt% (equivalent to 0 a.p.f.u.), and Y2O3 is 0 wt% (equivalent to 0 a.p.f.u.). The abundance of the REEs in pyroclore at the Panda Hill Carbonatite deposit is of no economic significance.
Abstract: The article gives new experimental data on spectral characteristics of photoluminescence of natural diamonds extracted from deep horizons of Mir and Internatsionalnaya Pipes, Republic of Sakha (Yakutia) depending on composition of basic and additional optically active structural defects in crystals and on temperature during spectrum recording, considering kinetics of luminescence. It is hypothesized on applicability of low-temperature effects to enhance efficiency of photoluminescence separation of diamond crystals.
Abstract: The Late Cretaceous Catalão I carbonatite complex consists of ultramafic silicate rocks, phoscorites, nelsonites and carbonatites. The latest stages of the evolution of the complex are characterized by several nelsonite (magnetite-apatite rock) and carbonatite dykes, plugs and veins crosscutting earlier alkaline rocks. The interaction between the latter and late-stage carbonatites and/or carbo-hydrothermal fluids, converted the original dunites and bebedourites to metasomatic phlogopitites. Late-stage nelsonites (N1), pseudonelsonites (N2) and various types of dolomite carbonatites (DC) including norsethite-, magnesite- and/or monazite-bearing varieties show significant whole-rock Nd and Sr isotopic variations. To elucidate whether magmatic or metasomatic processes, or both, were responsible for these isotope variations we characterized the Nd and Sr isotope compositions of major mineral phases (i.e. apatite, dolomite, norsethite, pyrochlore and tetraferriphlogopite) in these late-stage rocks. Mineral isotope data recorded the same differences observed between N1 and N2 whole-rocks with N2 minerals showing more enriched isotopic signatures than minerals from N1. Sr isotopic disequilibrium among minerals from N2 pseudonelsonites and spatially related dolomite carbonatite pockets implies formation from batches of carbonate melts with distinct isotopic compositions. A detailed investigation of Nd and Sr isotopes from whole-rocks and minerals suggests that the most evolved rocks of the Catalão I complex probably derive from two different evolution paths. We propose that an earlier magmatic trend (path A) could be explained by several batches of immiscible and/or residual melts derived from carbonated-silicate parental magma (e.g. phlogopite picrite) contaminated with continental crust to a variable extent, in an AFCLI-like process. A second trend (path B) comprises highly variable 143Nd/144Ndi at nearly constant 87Sr/86Sri coupled with high ?18O in carbonates. This is interpreted here as the result of the interaction of previously-formed dolomite carbonatites with carbo-hydrothermal fluids.
Diamond and Related Materials, Vol. 71, pp. 20-29,
Africa, Zimbabwe
Deposit - Marange
Abstract: This study gives an analysis of the effect of low-pressure, high-temperature annealing on the infrared, Raman, and photoluminescence (PL) features, as well as the inclusion characteristics, of cubo-octahedral diamond plates from the Marange deposits in Zimbabwe. The samples showed strong inclusion-related zoning which consists of micron-sized particles identified as graphite and these grew noticeably larger with annealing at temperatures of 300 °C to 1700 °C. Within the natural diamonds, the graphite inclusions (detected by Raman spectroscopy) had a grain size of approximately 1 ?m, which increased to 3 ?m after 1200 °C and 14 ?m after 1700 °C annealing and their hexagonal morphology was discernible. From the geometry of these grains, we determined that they were oriented within the {111} family of planes. The infrared absorption and PL spatial maps were collected after every temperature step to study the effects of annealing on the defects, and photomicrographs and Raman spectra were collected to study the graphite inclusions. The graphitic inclusions grew much larger as the stressed diamond surrounding them converted to graphite. Many nitrogen-related optical centers, including NV? and H3 are no longer detected after high temperature annealing within the cuboid regions as these may have been transformed to hydrogen-bearing complexes such as NVH and N2VH. The presence of CH4 is detected in the unannealed Marange diamonds, but was no longer observed in Raman spectra after 1200 °C annealing. This CH4 disappearance along with changes in inclusion morphology could provide a method to detect heat treatment if these mixed-habit samples are sourced to create treated black gem diamond.
Abstract: The paper presents new petrographic, major element and Fourier transform infrared (FTIR) spectroscopy data and PT-estimates of whole-rock samples and minerals of a collection of 19 relatively fresh peridotite xenoliths from the Udachnaya kimberlite pipe, which were recovered from its deeper levels. The xenoliths are non-deformed (granular), medium-deformed and highly deformed (porphyroclastic, mosaic-porphyroclastic, mylonitic) lherzolites, harzburgite and dunite. The lherzolites yielded equilibration temperatures (T) and pressures (P) ranging from 913 to 1324 °C and from 4.6 to 6.3 GPa, respectively. The non-deformed and medium-deformed peridotites match the 35 mW/m2 conductive continental geotherm, whereas the highly deformed varieties match the 45 mW/m2 geotherm. The content of water spans 2 ± 1-95 ± 52 ppm in olivine, 1 ± 0.5-61 ± 9 ppm in orthopyroxene, and 7 ± 2-71 ± 30 ppm in clinopyroxene. The amount of water in garnets is negligible. Based on the modal proportions of mineral phases in the xenoliths, the water contents in peridotites were estimated to vary over a wide range from < 1 to 64 ppm. The amount of water in the mantle xenoliths is well correlated with the deformation degree: highly deformed peridotites show highest water contents (64 ppm) and those medium-deformed and non-deformed contain ca. 1 ppm of H2O. The high water contents in the deformed peridotites could be linked to metasomatism of relatively dry diamondiferous cratonic roots by hydrous and carbonatitic agents (fluids/melts), which may cause hydration and carbonation of peridotite and oxidation and dissolution of diamonds. The heterogeneous distribution of water in the cratonic mantle beneath the Udachnaya pipe is consistent with the models of mantle plume or veined mantle structures proposed based on a trace element study of similar xenolithic suits. Mantle metasomatism beneath the Siberian Craton and its triggered kimberlite magmatism could be induced by mantle enrichment in volatiles (H2O, CO2) supplied by numerous subduction zones which surrounded the Siberian continent in Neoproterozoic-Cambrian time.
Abstract: In situ laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) and electron probe microanalysis (EPMA) are used to characterize magnetite and ilmenite of the phoscorite-carbonatite association at Phalaborwa. We trace the behavior of the compatible elements for two different generations of magnetite related to (1) a magmatic stage, with variable Ti-V content, which pre-dates the copper mineralization, and (2) a late hydrothermal, low-Ti, low-temperature event, mostly post-dating sulfide formation. Magnetite is shown to be a robust petrogenetic indicator; no influence on its chemical composition is detected from the intergrowth with the accompanying phases, including the interaction with coexisting sulfides. High spatial resolution EPMA characterize the tiny late-stage hydrothermal magnetite veins, as well as the ilmenite granular and lamellar exsolutions mostly developed in the magnetite from the phoscorite. By combining geochemical data with geothermo-oxybarometry calculations for magnetite-ilmenite pairs, we infer that the most primitive magnetite probably formed at oxygen fugacity above the nickel nickel oxide (NNO) buffer, revealing an evolutionary trend of decreasing temperature and oxygen fugacity. Geochemical similarity exists between magnetite from phoscorite and carbonatite, thus supporting a common mantle source for the phoscorite-carbonatite association.
Abstract: In-situ trace element analyses of fluorapatite, calcite, dolomite, olivine, and phlogopite have been undertaken on representative phoscorite and carbonatite rocks of the Palaeoproterozoic Phalaborwa Complex. Textural and compositional characterization reveals uniformity of fluorapatite and calcite among most of the intrusions, and seems to favor a common genetic origin for the phoscorite-carbonatite association. Representing major repositories for rare earth elements (REE), fluorapatite and calcite exhibit tightly correlated light REE (LREE) abundances, suggesting that partitioning of LREE into these rock forming minerals was principally controlled by simple igneous differentiation. However, light rare earth element distribution in apatite and calcite cannot be adequately explained by equilibrium and fractional crystallization and instead favors a complex crystallization history involving mixing of compositionally distinct magma batches, in agreement with previously reported mineral isotope variability that requires open-system behaviour.
Abstract: Uneconomical two decades ago, the Letseng diamond mine in Lesotho is today a major source of 50-carat-plus Type IIa diamonds. It is also the lowest-yielding diamond mine in the world, averaging about 1.5 carats of diamonds per hundred tons of ore against an industry average of one carat per ton. First opened in 1975, the previous operators of the mine (Rio Tinto and De Beers) struggled to maintain its operation because very large diamonds were mixed in with its very low production. The mine closed in 1982 after seven years of loss-making operation. In the 2000’s, three changes profoundly affected the diamond industry: 1. The price of large diamonds appreciated very strongly compared to more commercial sizes and qualities, 2. Improvements in ore processing technology that reduces potential damage or outright destruction of large crystals, and 3. Improvements in X-Ray technology that enhances the ability to identify low fluorescence, Type IIa and fancy color diamonds. This technology also allows for identification of very large diamonds in kimberlite before primary crushing. Letseng reopened in 2006 and has been operating at a profit despite its very low yield and relatively low volume, of about 100,000 carats yearly. The company continues to upgrade its technology which resulted in the recovery of 90 diamonds larger than 50 carats last year. Letseng also serves as a model for other small “boutique” mines such as Kerowe, the Botswana operation which yielded the 1109 ct Lesedi la Rona diamond in 2015 and the Lulo concession in Angola which have come on line recently.
Abstract: The Bayan Obo deposit in Inner Mongolia, North China Craton (NCC) is the largest rare-earth element (REE) resource in the world. Due to the complex element and mineral compositions and the activity of several geological events, the ore-forming mechanism is still controversial. Previous models are reviewed here to provide information for further investigation on the Bayan Obo deposit. In this study, we summarize all different types of Fe-REE-Nb mineralization using field observations and microscope work, in which we recognize 9 types of Fe-REE-Nb ores in the Bayan Obo ore district. By compiling and re-evaluating a large number of published geochemical data, this paper provides solid evidence that the Bayan Obo deposit formed through interaction between sedimentary rocks and carbonatite magmatism. From the results of our review, it can be conjectured that the formation of iron ores was originated from sedimentation (Pt1), whereas the formation of REE mineralized dolomite might be related to interaction and reaction between the carbonatite magmas and/or associated fluids with sedimentary carbonate rocks, with the REE-bearing carbonatite magmas having undergone intense fractionation enrichment process. The C-O-S-Fe-Mg isotopes indicate that the REE-Nb mineralization was derived from metasomatism (fenitic alteration) of sedimentary carbonate. A new model is proposed for this unique REE-Nb mineralization, which is related to the subduction of Siberian Craton beneath the North China Craton since Early Paleozoic period. We interpret that the Bayan Obo Fe-REE-Nb ore deposits and their massive barren host, H8 dolomite, were generated as a result of interaction of fluids expelled from a subcontinental lithospheric mantle (SCLM)-derived carbonatite magma with sedimentary carbonates.
Abstract: Mineral inclusions in diamonds have been used to track potential information on the Earth's deep mantle. Here we report results from a detailed study on the mineral inclusions in a ca. 0.28 ct diamond from the Shengli No. 1 kimberlite in Mengyin County, Shandong Province, eastern China. Our study reveals the presence of ?-quartz, albite and olivine in the diamond. At an inferred depth of ca. 165 km for the diamond crystallization, the inclusions of ?-quartz and albite suggest the possible involvement of deep subducted crustal material, traces of which were captured during the diamond growth and magma migration.
Abstract: Induced polarization (IP) effects are becoming more evident in time-domain helicopter airborne electromagnetic (AEM) data thanks to advances in instrumentation, mainly due to improvements in the signal-to-noise ratio and hence better data quality. Although the IP effects are often manifested as negative receiver voltage values, which are easy to detect, in some cases, IP effects can distort recovered transients in other ways so they may be less obvious and require careful data analysis and processing. These effects represent a challenge for modeling and inversion of the AEM data. For proper modeling of electromagnetic transients, the chargeability of the subsurface and other parameters describing the dispersion also need to be taken into consideration. We use the Cole-Cole model to characterize the dispersion and for modeling of the IP effects in field AEM data, collected by different airborne systems over different geologies and exploration targets, including examples from diamond, gold, and base metal exploration.
Earth and Planetary Science Letters, Vol. 463, pp. 178-188.
Africa, Botswana
Deposit - Lethakane
Abstract: Monocrystalline diamonds commonly record complex internal structures reflecting episodic growth linked to changing carbon-bearing fluids in the mantle. Using diamonds to trace the evolution of the deep carbon cycle therefore requires dating of individual diamond growth zones. To this end Rb-Sr and Sm-Nd isotope data are presented from individual eclogitic silicate inclusions from the Orapa and Letlhakane diamond mines, Botswana. ?13C?13C values are reported from the host diamond growth zones. Heterogeneous 87Sr/86Sr ratios (0.7033-0.7097) suggest inclusion formation in multiple and distinct tectono-magmatic environments. Sm-Nd isochron ages were determined based on groups of inclusions with similar trace element chemistry, Sr isotope ratios, and nitrogen aggregation of the host diamond growth zone. Diamond growth events at 0.14±0.090.14±0.09, 0.25±0.040.25±0.04, 1.1±0.091.1±0.09, 1.70±0.341.70±0.34 and 2.33±0.022.33±0.02 Ga can be directly related to regional tectono-magmatic events. Individual diamonds record episodic growth with age differences of up to 2 Ga. Dated diamond zones have variable ?13C?13C values (?5.0 to ?33.6‰ vs PDB) and appear to imply changes in subducted material over time. The studied Botswanan diamonds are interpreted to have formed in different tectono-magmatic environments that involve mixing of carbon from three sources that represent: i) subducted biogenic sediments (lightest ?13C?13C, low 87Sr/86Sr); ii) subducted carbonate-rich sediments (heavy ?13C?13C, high 87Sr/86Sr) and iii) depleted upper mantle (heavy ?13C?13C, low 87Sr/86Sr). We infer that older diamonds from these two localities are more likely to have light ?13C?13C due to greater subduction of biogenic sediments that may be related to hotter and more reduced conditions in the Archaean before the Great Oxidation Event at 2.3 Ga. These findings imply a marked temporal change in the nature of subducted carbon beneath Botswana and warrant further study to establish if this is a global phenomenon.
Abstract: The Bayan Obo in the northern North China Craton (NCC) is the world’s largest light rare earth element (LREE) deposit and is hosted in carbonatite sills emplaced into sedimentary rocks of the Bayan Obo Group. However, the timing and genesis of the Bayan Obo deposit has been highly controversial for many decades. Here we report a precise zircon 208Pb/232Th age of 1301 ± 12 Ma (N = 47, mean square of weighted deviates [MSWD] = 2.2) for a REE-Nb-rich carbonatite sill from the Bayan Obo deposit. Zircon morphology, trace element compositions and mineral inclusions demonstrate that these zircons were crystallized from REE-Nb-rich carbonatitic magmas and their ages represent the timing of carbonatites and REE-Nb mineralization. The newly obtained age of ca. 1.30 Ga is consistent with field observations of the Bayan Obo REE-Nb deposit and successfully explains why the carbonatites and REE-Nb mineralization in the Bayan Obo deposit occurred mainly in the Jianshan Formation and that no carbonatites and REE-Nb mineralization were identified from the rocks overlying the Jianshan Formation. The new results demonstrate that the Bayan Obo REE-Nb deposit is a product of mantle-derived carbonatite magmatism at ca. 1.30 Ga. Field relations show that emplacement of the Bayan Obo carbonatites was accompanied by pre-magmatic uplift that is considered to be related to rift-to-drift transition. The Bayan Obo carbonatites and REE-Nb deposit are spatially and temporally linked with the newly identified 1.33-1.30 Ga Yanliao large igneous province (LIP) in the northern NCC and were related to continental rifting that have led to breakup of the NCC from the Columbia (Nuna) supercontinent.
Earth and Planetary Science Letters, Vol. 465, pp. 208-227.
Russia
Deposit - Udachnaya-East
Abstract: The critical issue in the study of kimberlites, known as principal host rocks of diamonds, is the reconstruction of their primary melt composition, which is poorly constrained due to contamination by xenogenic materials, significant loss of volatiles during eruption, and post-magmatic alteration. It is generally accepted that the last equilibration of primary kimberlite melt with surrounding mantle (garnet lherzolite) occurred beneath cratons at 5-7 GPa (150-230 km depths). However, the subliquidus mineral assemblages obtained in kimberlite melting experiments at mantle pressures differ from lherzolite, probably owing to unaccounted loss of CO2. Here we present experiments at 6.5 GPa and 1200-1600 °C on unaltered kimberlite with an addition of 2-22 mol% CO2 over its natural abundance in the rock (13 mol%), but keeping proportions of other components identical to those in an exceptionally fresh anhydrous kimberlite from Udachnaya-East pipe in Siberia. We found that the partial melt achieves equilibrium with garnet lherzolite at 1500 °C and 19-23 mol% CO2 in the system. Under these conditions this melt contains (mol%): SiO2 = 9, FeO = 6-7, MgO = 23-26, CaO = 16, Na2O = 4, K2O = 1, and CO2 = 30-35. We propose, therefore, the alkali-rich carbonatitic composition of primary kimberlite melt and loss of 34-45 mol% (34-46 wt%) CO2 during ascent of the kimberlite magma to the surface.
Journal of Petrology, Vol. 57, 11-12, pp. 2251-2270.
Africa, Morocco
Deposit - Beni Bousera
Abstract: Correlations between major and minor transition elements in tectonically emplaced orogenic peridotites have been ascribed to variable degrees of melt extraction and melt-rock reaction processes, leading to depletion or refertilization. To elucidate how such processes are recorded in the subcontinental lithospheric mantle, we processed a large geochemical dataset for peridotites from the four tectono-metamorphic domains of the Beni Bousera orogenic massif (Rif Belt, northern Morocco). Our study reveals that variations in bulk-rock major and minor elements, Mg-number and modal mineralogy of lherzolites, as well as their clinopyroxene trace element compositions, are inconsistent with simple partial melting and mainly resulted from different reactions between melts and depleted peridotites. Up to 30% melting at <3 GPa and cryptic metasomatism can account for the geochemical variations of most harzburgites. In Grt-Sp mylonites, melting and melt-rock reactions are masked by tectonic mixing with garnet pyroxenites and subsolidus re-equilibration. In the rest of the massif, lherzolites were mostly produced by refertilization of a refractory protolith (Mg-number = 91, Ol = 70%, Cpx/Opx = 0.4) via two distinct near-solidus, melt- rock reactions: (1) clinopyroxene and orthopyroxene precipitation and olivine consumption at melt/rock ratios <0.75 and variable mass ratio between crystallized minerals and infiltrated melt ®, which are recorded fairly homogeneously throughout the massif; (2) dissolution of orthopyroxene and precipitation of clinopyroxene and olivine at melt/rock ratios <1 and R = 0.2-0.3, which affected mainly the Arie` gite-Seiland and Seiland domains. The distribution of secondary lherzolites in the massif suggests that the first refertilization reaction occurred prior to the differentiation of the Beni Bousera mantle section into petro-structural zones, whereas the second reaction was associated with the development of the tectono-metamorphic domains. Our data support a secondary, refertilization-related origin for most lherzolites in orogenic peridotite massifs.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 5374 Abstract
Russia
Deposit - Udachnaya
Abstract: The study of diamonds and the mineral inclusions trapped in them is of great interest for Earth science, since they can provide insight about deep mantle conditions and its evolution. The conventional techniques commonly used are destructive and thus do not allow the employment of different methods used simultaneously to obtain integrated and complementary results. Significant information about the growth conditions of diamonds and their inclusions still trapped within them can be preferably obtained by in situ investigation. In this study, we propose a multi-analytical approach, using a set of non-destructive techniques with conventional sources, to investigate one diamond from Udachnaya kimberlite (Siberia, Russia). The combined use of micro-X-ray Tomography, micro-X-ray Fluorescence, X-Ray Powder Diffraction and micro-Raman spectroscopy, allowed us to determine the spatial distribution of the inclusions, their chemical and mineralogical composition and, finally, the paragenetic suite, totally preserving the diamond host. The sample was also studied by means of X-ray Diffraction Topography to characterize the structural defects and to obtain genetic information about the growth history of the diamond. The combination of the different data provided a sort of «mapping» of a diamond. The X-Ray Topographic images show that the sample investigated exhibits plastic deformation. Actually, one set of {111} slip lamellae, corresponding to polysynthetic twinning, affect the whole sample. The tomographic images reveal that the primary inclusions, not observable optically, show a poly-faceted shape corresponding to an assemblage of tiny crystals. The chemical data display that the trapped minerals are mono-sulphides of Fe, Ni. The diagrams obtained by the X-Ray diffraction reveal that the inclusions mainly consist of an assemblage of tiny crystals of pentlandite and pyrrothite. Nevertheless, a thorough analysis of the diffraction data suggests the presence of another mono-sulphide of Fe,Ni: mackinawite. Raman spectra taken on these inclusions confirm, for the first time, the presence of this metastable phase as inclusion in diamond. The genetic implications of these results are discussed.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 12200 Abstract
Russia
Deposit - Udachnaya
Abstract: The correct determination of the relative crystallographic orientations of single crystals has many applications. When single crystals undergo phase transitions, especially at high pressures, the relative orientations of the two phases yields insights into transition mechanisms (Dobson et al 2013). On the other hand, determination of the crystallographic orientations of minerals included in diamonds can provide insights into the mechanisms of their entrapment and the timing of their formation relative to the host diamond (e.g. Nestola et al. 2014, Milani et al. 2016). The reported occurrence of non-trivial orientations for some minerals in diamonds, suggesting an epitaxial relationship, has long been considered to reflect contemporaneous growth of the diamond and the inclusion (e.g. syngenesis). Correct interpretation of such orientations requires (i) a statistically significant crystallographic data set for single and multiple inclusions in a large number of diamonds, and (ii) a robust data-processing method, capable of removing ambiguities derived from the high symmetry of the diamond and the inclusion. We have developed a software to perform such processing (OrientXplot, Angel et al. 2015), starting from crystallographic orientation matrixes obtained by X-ray diffractometry or EBSD data. Previous studies of inclusions in lithospheric diamonds, by single-crystal X-ray diffraction and EBSD, indicate a wide variety in the orientations of different inclusion phases with respect to their diamond host (Futergendler & Frank-Kamenetsky 1961; Frank-Kamenetsky 1964; Wiggers de Vries et al. 2011; Nestola et al. 2014, Milani et al. 2016). For example, olivine inclusions in lithospheric diamonds from Udachnaya do not show any preferred orientations with respect to their diamond hosts, but multiple inclusions in a single diamond often show very similar orientations within few degrees. In the present work on magnesiochromite inclusions in diamonds from Udachnaya, there is a partial orientation between inclusion and host. A (111) plane of each inclusion is sub-parallel to a {111} plane of their diamond host, but with random orientations of the magnesiochromite [100], [010] and [001] relative to the diamond. In one case, where a single inclusion comprised a magnesiochromite-olivine touching pair, the magnesiochromite was oriented as noted above and the olivine showed a random orientation. The implications of these observations for the mechanisms of diamond growth will be explored and the results will be compared and combined with previous work.
Ashchepkov, I., Ntaflos, T., Logvinova, A., Vladykin, N., Ivanov, A., Spetsius, Z., Stegnitsky, Y., Kostrovitsky, S., Salikhov, R., Makovchuk, I., Shmarov, G., Karpenko, M., Downes, H., Madvedev, N.
Abstract: The PTX diagrams for the separate phases in Sytykanskaya (Ashchepkov et al., 2016) Dalnyaya (Ashchepkov et al., 2017), pipes shows that the PK show the relatively simple P-X trends and geotherms and shows more contrast and simple layering. The PK contain most abundant material from the root of the magma generation they are dunitic veins as the magma feeders represented by the megacrysts. New results for the Aykhal, Zarya and Komsomolskaya pipes in Alake field and Zarnitsa and Udachnaya pipes in Daldyn field show that evolution is accompanied by the developing of metasomatites and branching and veining of the wall rock peridotites . In Aykhal pipe in PK the Gar- dunites prevail, the xenoliths from the dark ABK "Rebus" contain Cr-Ti - rich garnets and ilmenites, more abundant compared with the grey carbonited breccia Nearly the same features were found for Yubileinaya pipe. The example of Komsomolskya pipes show that the ABK contain more eclogitic xenolith than PK. The developing of the magma channel shown in satellite Chukukskaya and Structurnaya pipe was followed by the separation of some parts of the magmatic feeders and crystallization of abundant Gar megacrysts near o the walls blocking the peridotites from the magma feeder. This drastically decrease diamond grade of pipes. Such blocking seems to be the common features for the latest breccias. In Zarnitsa pipe, the dark PK and ABK also contain fresh xenoliths but not only dunites but also sheared and metasomatic varieties and eclogites. Most of dark ABK in Yakutia contain the intergrowth of ilmenites with brown Ti- Cpx showing joint evolution trends. The late breccia contains completely altered peridotite xenoliths mainly of dunite- harzburgite type. The comparison of the trace elements of the coexisting minerals in megacryst show that they were derived from the protokimberlites but are not in complete equilibrium as well as other megacrystalline phases. Ilmenites show inflections of the trace element patterns of most Ilmenites but more regular for the Cpx and Garnets revealing the sub parallel patterns elevating LREE with the rising TRE. But commonly these are not continuous sequances because they developed in the pulsing moving systems like beneath Zarnitsa. The minerals from the feeders like dunites also show the inflected or S-type REE patterns. From the earlier to later phases the TRE compositions became more evolved reflecting the evolution of protokimberlites. The wall rocks also often show the interaction with the more evolved melts and sometimes "cut" spectrums due to the dissolution some phases and repeated melting events So we could suggest the joint evolution of the mantle column protokimberlites and megacrysts composition and type of kimberlites with the diamond grade. The mantle lithospheric base captured by the PK. The developing and rising protokimbelrites was followed by the crystallization of the diamonds in the gradient in FO2 zone in wall rocks due to reductions of C -bearing fluids and carbonatites (> 1 QMF) on peridotites ((< -2 -5 QMF). The most intensive reactions are near the graphite - diamond boundary where protokimberlites are breaking and where most framesites are forming.
Ashchepkov, I., Ntaflos, T., Logvinova, A., Vladykin, N., Ivanov, A., Spetsius, Z., Stegnitsky, Y., Kostrovitsky, S., Salikhov, R., Makovchuk, I., Shmarov, G., Karpenko, M., Downes, H., Madvedev, N.
Abstract: The PTX diagrams for the separate phases in Sytykanskaya (Ashchepkov et al., 2016) Dalnyaya (Ashchepkov et al., 2017), pipes shows that the PK show the relatively simple P-X trends and geotherms and shows more contrast and simple layering. The PK contain most abundant material from the root of the magma generation they are dunitic veins as the magma feeders represented by the megacrysts. New results for the Aykhal, Zarya and Komsomolskaya pipes in Alake field and Zarnitsa and Udachnaya pipes in Daldyn field show that evolution is accompanied by the developing of metasomatites and branching and veining of the wall rock peridotites . In Aykhal pipe in PK the Gar- dunites prevail, the xenoliths from the dark ABK "Rebus" contain Cr-Ti - rich garnets and ilmenites, more abundant compared with the grey carbonited breccia Nearly the same features were found for Yubileinaya pipe. The example of Komsomolskya pipes show that the ABK contain more eclogitic xenolith than PK. The developing of the magma channel shown in satellite Chukukskaya and Structurnaya pipe was followed by the separation of some parts of the magmatic feeders and crystallization of abundant Gar megacrysts near o the walls blocking the peridotites from the magma feeder. This drastically decrease diamond grade of pipes. Such blocking seems to be the common features for the latest breccias. In Zarnitsa pipe, the dark PK and ABK also contain fresh xenoliths but not only dunites but also sheared and metasomatic varieties and eclogites. Most of dark ABK in Yakutia contain the intergrowth of ilmenites with brown Ti- Cpx showing joint evolution trends. The late breccia contains completely altered peridotite xenoliths mainly of dunite- harzburgite type. The comparison of the trace elements of the coexisting minerals in megacryst show that they were derived from the protokimberlites but are not in complete equilibrium as well as other megacrystalline phases. Ilmenites show inflections of the trace element patterns of most Ilmenites but more regular for the Cpx and Garnets revealing the sub parallel patterns elevating LREE with the rising TRE. But commonly these are not continuous sequances because they developed in the pulsing moving systems like beneath Zarnitsa. The minerals from the feeders like dunites also show the inflected or S-type REE patterns. From the earlier to later phases the TRE compositions became more evolved reflecting the evolution of protokimberlites. The wall rocks also often show the interaction with the more evolved melts and sometimes "cut" spectrums due to the dissolution some phases and repeated melting events So we could suggest the joint evolution of the mantle column protokimberlites and megacrysts composition and type of kimberlites with the diamond grade. The mantle lithospheric base captured by the PK. The developing and rising protokimbelrites was followed by the crystallization of the diamonds in the gradient in FO2 zone in wall rocks due to reductions of C -bearing fluids and carbonatites (> 1 QMF) on peridotites ((< -2 -5 QMF). The most intensive reactions are near the graphite - diamond boundary where protokimberlites are breaking and where most framesites are forming.
Ashchepkov, I., Ntaflos, T., Logvinova, A., Vladykin, N., Ivanov, A., Spetsius, Z., Stegnitsky, Y., Kostrovitsky, S., Salikhov, R., Makovchuk, I., Shmarov, G., Karpenko, M., Downes, H., Madvedev, N.
Abstract: The PTX diagrams for the separate phases in Sytykanskaya (Ashchepkov et al., 2016) Dalnyaya (Ashchepkov et al., 2017), pipes shows that the PK show the relatively simple P-X trends and geotherms and shows more contrast and simple layering. The PK contain most abundant material from the root of the magma generation they are dunitic veins as the magma feeders represented by the megacrysts. New results for the Aykhal, Zarya and Komsomolskaya pipes in Alake field and Zarnitsa and Udachnaya pipes in Daldyn field show that evolution is accompanied by the developing of metasomatites and branching and veining of the wall rock peridotites . In Aykhal pipe in PK the Gar- dunites prevail, the xenoliths from the dark ABK "Rebus" contain Cr-Ti - rich garnets and ilmenites, more abundant compared with the grey carbonited breccia Nearly the same features were found for Yubileinaya pipe. The example of Komsomolskya pipes show that the ABK contain more eclogitic xenolith than PK. The developing of the magma channel shown in satellite Chukukskaya and Structurnaya pipe was followed by the separation of some parts of the magmatic feeders and crystallization of abundant Gar megacrysts near o the walls blocking the peridotites from the magma feeder. This drastically decrease diamond grade of pipes. Such blocking seems to be the common features for the latest breccias. In Zarnitsa pipe, the dark PK and ABK also contain fresh xenoliths but not only dunites but also sheared and metasomatic varieties and eclogites. Most of dark ABK in Yakutia contain the intergrowth of ilmenites with brown Ti- Cpx showing joint evolution trends. The late breccia contains completely altered peridotite xenoliths mainly of dunite- harzburgite type. The comparison of the trace elements of the coexisting minerals in megacryst show that they were derived from the protokimberlites but are not in complete equilibrium as well as other megacrystalline phases. Ilmenites show inflections of the trace element patterns of most Ilmenites but more regular for the Cpx and Garnets revealing the sub parallel patterns elevating LREE with the rising TRE. But commonly these are not continuous sequances because they developed in the pulsing moving systems like beneath Zarnitsa. The minerals from the feeders like dunites also show the inflected or S-type REE patterns. From the earlier to later phases the TRE compositions became more evolved reflecting the evolution of protokimberlites. The wall rocks also often show the interaction with the more evolved melts and sometimes "cut" spectrums due to the dissolution some phases and repeated melting events So we could suggest the joint evolution of the mantle column protokimberlites and megacrysts composition and type of kimberlites with the diamond grade. The mantle lithospheric base captured by the PK. The developing and rising protokimbelrites was followed by the crystallization of the diamonds in the gradient in FO2 zone in wall rocks due to reductions of C -bearing fluids and carbonatites (> 1 QMF) on peridotites ((< -2 -5 QMF). The most intensive reactions are near the graphite - diamond boundary where protokimberlites are breaking and where most framesites are forming.
Ashchepkov, I., Ntaflos, T., Logvinova, A., Vladykin, N., Ivanov, A., Spetsius, Z., Stegnitsky, Y., Kostrovitsky, S., Salikhov, R., Makovchuk, I., Shmarov, G., Karpenko, M., Downes, H., Madvedev, N.
Abstract: The PTX diagrams for the separate phases in Sytykanskaya (Ashchepkov et al., 2016) Dalnyaya (Ashchepkov et al., 2017), pipes shows that the PK show the relatively simple P-X trends and geotherms and shows more contrast and simple layering. The PK contain most abundant material from the root of the magma generation they are dunitic veins as the magma feeders represented by the megacrysts. New results for the Aykhal, Zarya and Komsomolskaya pipes in Alake field and Zarnitsa and Udachnaya pipes in Daldyn field show that evolution is accompanied by the developing of metasomatites and branching and veining of the wall rock peridotites . In Aykhal pipe in PK the Gar- dunites prevail, the xenoliths from the dark ABK "Rebus" contain Cr-Ti - rich garnets and ilmenites, more abundant compared with the grey carbonited breccia Nearly the same features were found for Yubileinaya pipe. The example of Komsomolskya pipes show that the ABK contain more eclogitic xenolith than PK. The developing of the magma channel shown in satellite Chukukskaya and Structurnaya pipe was followed by the separation of some parts of the magmatic feeders and crystallization of abundant Gar megacrysts near o the walls blocking the peridotites from the magma feeder. This drastically decrease diamond grade of pipes. Such blocking seems to be the common features for the latest breccias. In Zarnitsa pipe, the dark PK and ABK also contain fresh xenoliths but not only dunites but also sheared and metasomatic varieties and eclogites. Most of dark ABK in Yakutia contain the intergrowth of ilmenites with brown Ti- Cpx showing joint evolution trends. The late breccia contains completely altered peridotite xenoliths mainly of dunite- harzburgite type. The comparison of the trace elements of the coexisting minerals in megacryst show that they were derived from the protokimberlites but are not in complete equilibrium as well as other megacrystalline phases. Ilmenites show inflections of the trace element patterns of most Ilmenites but more regular for the Cpx and Garnets revealing the sub parallel patterns elevating LREE with the rising TRE. But commonly these are not continuous sequances because they developed in the pulsing moving systems like beneath Zarnitsa. The minerals from the feeders like dunites also show the inflected or S-type REE patterns. From the earlier to later phases the TRE compositions became more evolved reflecting the evolution of protokimberlites. The wall rocks also often show the interaction with the more evolved melts and sometimes "cut" spectrums due to the dissolution some phases and repeated melting events So we could suggest the joint evolution of the mantle column protokimberlites and megacrysts composition and type of kimberlites with the diamond grade. The mantle lithospheric base captured by the PK. The developing and rising protokimbelrites was followed by the crystallization of the diamonds in the gradient in FO2 zone in wall rocks due to reductions of C -bearing fluids and carbonatites (> 1 QMF) on peridotites ((< -2 -5 QMF). The most intensive reactions are near the graphite - diamond boundary where protokimberlites are breaking and where most framesites are forming.
Ashchepkov, I., Ntaflos, T., Logvinova, A., Vladykin, N., Ivanov, A., Spetsius, Z., Stegnitsky, Y., Kostrovitsky, S., Salikhov, R., Makovchuk, I., Shmarov, G., Karpenko, M., Downes, H., Madvedev, N.
Abstract: The PTX diagrams for the separate phases in Sytykanskaya (Ashchepkov et al., 2016) Dalnyaya (Ashchepkov et al., 2017), pipes shows that the PK show the relatively simple P-X trends and geotherms and shows more contrast and simple layering. The PK contain most abundant material from the root of the magma generation they are dunitic veins as the magma feeders represented by the megacrysts. New results for the Aykhal, Zarya and Komsomolskaya pipes in Alake field and Zarnitsa and Udachnaya pipes in Daldyn field show that evolution is accompanied by the developing of metasomatites and branching and veining of the wall rock peridotites . In Aykhal pipe in PK the Gar- dunites prevail, the xenoliths from the dark ABK "Rebus" contain Cr-Ti - rich garnets and ilmenites, more abundant compared with the grey carbonited breccia Nearly the same features were found for Yubileinaya pipe. The example of Komsomolskya pipes show that the ABK contain more eclogitic xenolith than PK. The developing of the magma channel shown in satellite Chukukskaya and Structurnaya pipe was followed by the separation of some parts of the magmatic feeders and crystallization of abundant Gar megacrysts near o the walls blocking the peridotites from the magma feeder. This drastically decrease diamond grade of pipes. Such blocking seems to be the common features for the latest breccias. In Zarnitsa pipe, the dark PK and ABK also contain fresh xenoliths but not only dunites but also sheared and metasomatic varieties and eclogites. Most of dark ABK in Yakutia contain the intergrowth of ilmenites with brown Ti- Cpx showing joint evolution trends. The late breccia contains completely altered peridotite xenoliths mainly of dunite- harzburgite type. The comparison of the trace elements of the coexisting minerals in megacryst show that they were derived from the protokimberlites but are not in complete equilibrium as well as other megacrystalline phases. Ilmenites show inflections of the trace element patterns of most Ilmenites but more regular for the Cpx and Garnets revealing the sub parallel patterns elevating LREE with the rising TRE. But commonly these are not continuous sequances because they developed in the pulsing moving systems like beneath Zarnitsa. The minerals from the feeders like dunites also show the inflected or S-type REE patterns. From the earlier to later phases the TRE compositions became more evolved reflecting the evolution of protokimberlites. The wall rocks also often show the interaction with the more evolved melts and sometimes "cut" spectrums due to the dissolution some phases and repeated melting events So we could suggest the joint evolution of the mantle column protokimberlites and megacrysts composition and type of kimberlites with the diamond grade. The mantle lithospheric base captured by the PK. The developing and rising protokimbelrites was followed by the crystallization of the diamonds in the gradient in FO2 zone in wall rocks due to reductions of C -bearing fluids and carbonatites (> 1 QMF) on peridotites ((< -2 -5 QMF). The most intensive reactions are near the graphite - diamond boundary where protokimberlites are breaking and where most framesites are forming.
Ashchepkov, I., Ntaflos, T., Logvinova, A., Vladykin, N., Ivanov, A., Spetsius, Z., Stegnitsky, Y., Kostrovitsky, S., Salikhov, R., Makovchuk, I., Shmarov, G., Karpenko, M., Downes, H., Madvedev, N.
Abstract: The PTX diagrams for the separate phases in Sytykanskaya (Ashchepkov et al., 2016) Dalnyaya (Ashchepkov et al., 2017), pipes shows that the PK show the relatively simple P-X trends and geotherms and shows more contrast and simple layering. The PK contain most abundant material from the root of the magma generation they are dunitic veins as the magma feeders represented by the megacrysts. New results for the Aykhal, Zarya and Komsomolskaya pipes in Alake field and Zarnitsa and Udachnaya pipes in Daldyn field show that evolution is accompanied by the developing of metasomatites and branching and veining of the wall rock peridotites . In Aykhal pipe in PK the Gar- dunites prevail, the xenoliths from the dark ABK "Rebus" contain Cr-Ti - rich garnets and ilmenites, more abundant compared with the grey carbonited breccia Nearly the same features were found for Yubileinaya pipe. The example of Komsomolskya pipes show that the ABK contain more eclogitic xenolith than PK. The developing of the magma channel shown in satellite Chukukskaya and Structurnaya pipe was followed by the separation of some parts of the magmatic feeders and crystallization of abundant Gar megacrysts near o the walls blocking the peridotites from the magma feeder. This drastically decrease diamond grade of pipes. Such blocking seems to be the common features for the latest breccias. In Zarnitsa pipe, the dark PK and ABK also contain fresh xenoliths but not only dunites but also sheared and metasomatic varieties and eclogites. Most of dark ABK in Yakutia contain the intergrowth of ilmenites with brown Ti- Cpx showing joint evolution trends. The late breccia contains completely altered peridotite xenoliths mainly of dunite- harzburgite type. The comparison of the trace elements of the coexisting minerals in megacryst show that they were derived from the protokimberlites but are not in complete equilibrium as well as other megacrystalline phases. Ilmenites show inflections of the trace element patterns of most Ilmenites but more regular for the Cpx and Garnets revealing the sub parallel patterns elevating LREE with the rising TRE. But commonly these are not continuous sequances because they developed in the pulsing moving systems like beneath Zarnitsa. The minerals from the feeders like dunites also show the inflected or S-type REE patterns. From the earlier to later phases the TRE compositions became more evolved reflecting the evolution of protokimberlites. The wall rocks also often show the interaction with the more evolved melts and sometimes "cut" spectrums due to the dissolution some phases and repeated melting events So we could suggest the joint evolution of the mantle column protokimberlites and megacrysts composition and type of kimberlites with the diamond grade. The mantle lithospheric base captured by the PK. The developing and rising protokimbelrites was followed by the crystallization of the diamonds in the gradient in FO2 zone in wall rocks due to reductions of C -bearing fluids and carbonatites (> 1 QMF) on peridotites ((< -2 -5 QMF). The most intensive reactions are near the graphite - diamond boundary where protokimberlites are breaking and where most framesites are forming.
Ashchepkov, I., Ntaflos, T., Logvinova, A., Vladykin, N., Ivanov, A., Spetsius, Z., Stegnitsky, Y., Kostrovitsky, S., Salikhov, R., Makovchuk, I., Shmarov, G., Karpenko, M., Downes, H., Madvedev, N.
Abstract: The PTX diagrams for the separate phases in Sytykanskaya (Ashchepkov et al., 2016) Dalnyaya (Ashchepkov et al., 2017), pipes shows that the PK show the relatively simple P-X trends and geotherms and shows more contrast and simple layering. The PK contain most abundant material from the root of the magma generation they are dunitic veins as the magma feeders represented by the megacrysts. New results for the Aykhal, Zarya and Komsomolskaya pipes in Alake field and Zarnitsa and Udachnaya pipes in Daldyn field show that evolution is accompanied by the developing of metasomatites and branching and veining of the wall rock peridotites . In Aykhal pipe in PK the Gar- dunites prevail, the xenoliths from the dark ABK "Rebus" contain Cr-Ti - rich garnets and ilmenites, more abundant compared with the grey carbonited breccia Nearly the same features were found for Yubileinaya pipe. The example of Komsomolskya pipes show that the ABK contain more eclogitic xenolith than PK. The developing of the magma channel shown in satellite Chukukskaya and Structurnaya pipe was followed by the separation of some parts of the magmatic feeders and crystallization of abundant Gar megacrysts near o the walls blocking the peridotites from the magma feeder. This drastically decrease diamond grade of pipes. Such blocking seems to be the common features for the latest breccias. In Zarnitsa pipe, the dark PK and ABK also contain fresh xenoliths but not only dunites but also sheared and metasomatic varieties and eclogites. Most of dark ABK in Yakutia contain the intergrowth of ilmenites with brown Ti- Cpx showing joint evolution trends. The late breccia contains completely altered peridotite xenoliths mainly of dunite- harzburgite type. The comparison of the trace elements of the coexisting minerals in megacryst show that they were derived from the protokimberlites but are not in complete equilibrium as well as other megacrystalline phases. Ilmenites show inflections of the trace element patterns of most Ilmenites but more regular for the Cpx and Garnets revealing the sub parallel patterns elevating LREE with the rising TRE. But commonly these are not continuous sequances because they developed in the pulsing moving systems like beneath Zarnitsa. The minerals from the feeders like dunites also show the inflected or S-type REE patterns. From the earlier to later phases the TRE compositions became more evolved reflecting the evolution of protokimberlites. The wall rocks also often show the interaction with the more evolved melts and sometimes "cut" spectrums due to the dissolution some phases and repeated melting events So we could suggest the joint evolution of the mantle column protokimberlites and megacrysts composition and type of kimberlites with the diamond grade. The mantle lithospheric base captured by the PK. The developing and rising protokimbelrites was followed by the crystallization of the diamonds in the gradient in FO2 zone in wall rocks due to reductions of C -bearing fluids and carbonatites (> 1 QMF) on peridotites ((< -2 -5 QMF). The most intensive reactions are near the graphite - diamond boundary where protokimberlites are breaking and where most framesites are forming.
Journal of Mining Science, Vol. 52, 2, pp. 388-393.
Russia
Deposit - Nyurbisnskaya
Abstract: The designed automated system for pitwall deformation monitoring consists of an independent data recorder, strain sensors, AD converters, and front-end and back-end controls. Data are accumulated on server in on-line mode via cellular modem. The self-contained tools are supplied from accumulators recharged by solar batteries, which expands operational life of the system. The system has been trailed in an open pit mine at Nyurbinskaya kimberlite pipe in deformation monitoring of faults in the eastern pitwall and estimation of its stability.
Cr-diopsides from Lattavaram and Kalyanadurgam kimberlites, Anatapur district, Andhra Praseh, southern India: inferences from loam sampling.
Department of Geophysics, University College of Science Osmania University, Hyderabad 500 007, March 16, 17, Role of Geophysics in Earth and Environmental studies: special emphasis on mineral exploration 1p. Abstract
Cr-diopsides from Lattavaram and Kalyanadurgam kimberlites, Anatapur district, Andhra Praseh, southern India: inferences from loam sampling.
Department of Geophysics, University College of Science Osmania University, Hyderabad 500 007, March 16, 17, Role of Geophysics in Earth and Environmental studies: special emphasis on mineral exploration 1p. Abstract
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 5540 Abstract
Africa, Botswana
Deposit - Letlhakane
Abstract: The diamondiferous Letlhakane kimberlites are part of the Orapa kimberlite cluster (˜ 93.1 Ma) in north-eastern Botswana, located on the edge of the Zimbabwe Craton, close to the Proterozoic Magondi Mobile Belt. Here we report the first Re-Os ages of six individual eclogitic sulphide inclusions (3.0 to 35.7?g) from Letlhakane diamonds along with their rhenium, osmium, iridium and platinum concentrations, and carbon isotope, nitrogen content and N-aggregation data from the corresponding growth zones of the host diamonds. For the first time, Re-Os data will be compared to Sm-Nd ages of individual eclogitic silicate inclusions recovered from the same diamonds using a Triton Plus equipped with four 1013? amplifiers. The analysed inclusion set currently encompasses pairs of individual sulphides from two diamonds (LK040 sf4 & 5, LK113 sf1 & 2) and two sulphide inclusions from separate diamonds (LK048, LK362). Ongoing work will determine the Sm-Nd ages and element composition of multiple individual eclogitic garnets (LK113/LK362, n=4) and an eclogitic clinopyroxene (LK040) inclusion. TMA ages of the six sulphides range from 1.06 to 2.38 Ga (± 0.1 to 0.54 Ga) with Re and Os contents between 7 and 68 ppb and 0.03 and 0.3 ppb, respectively. The host diamond growth zones have low nitrogen abundances (21 to 43 ppm N) and high N-aggregation (53 to 90% IaB). Carbon isotope data suggests the involvement of crustal carbon (?13C between -19.3 to -22.7 ± 0.2 per mill) during diamond precipitation. Cathodoluminescence imaging of central plates from LK040 and LK113 displays homogenous internal structure with no distinct zonation. The two sulphide inclusions from LK040 define an 'isochron' of 0.92 ± 0.23 Ga (2SD) with initial 187Os/188Os = 1.31 ± 0.24. Sulphides from LK113 have clear imposed diamond morphology and indicate diamond formation at 0.93 ± 0.36 Ga (2SD) with initial 187Os/188Os = 0.69 ± 0.44. The variation in the initial 187Os/188Os does not justify including these inclusions (or any from other diamonds) on the same isochron and implies an extremely heterogeneous diamond crystallisation environment that incorporated recycled Os. C1-normalized osmium, iridium and platinum (PGE) compositions from the analysed sulphide inclusions display enrichment in Ir (3.4 to 33) and Pt (2.3 to 28.1) in comparison to eclogitic xenolith data from Orapa that are depleted relative to chondrite. The Re-Os isochrons determined in this study are within error of previously reported ages from the adjacent (˜40km) Orapa diamond mine (1.0 to 2.9 Ga) based on sulphide inclusions and a multi-point 990 ± 50 Ma (2SD) isochron for composite (n=730) silicate inclusions. Together with additional new Sm-Nd isochron age determinations from individual silicate inclusions from Letlhakane (2.3 ± 0.02 (n = 3); 1.0 ± 0.14 (n = 4) and 0.25 ± 0.04 Ga (n = 3), all 2SE) these data suggest a phase of Mesoproterozoic diamond formation as well as Neoarchean/Paleoproterozoic and Mesozoic diamond growth, in punctuated events spanning >2.0 Ga.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 16438 Abstract
Africa, Zimbabwe, Australia, South America, Brazil
Deposit - Murowa, Argyle, Machado River
Abstract: Fourier Transform Infrared (FTIR) spectroscopy is a commonly-used technique for investigating diamonds. It gives the most useful information if spatially-resolved measurements are used [1]. In this contribution we discuss the best way to acquire and present FTIR data from diamonds, using examples from Murowa (Zimbabwe), Argyle (Australia) and Machado River (Brazil). Examples of FTIR core-to-rim line scans, maps with high spatial resolution and maps with high spectral resolution that are fitted to extract the spatial variation of different nitrogen and hydrogen defects are presented. Model mantle residence temperatures are calculated from the concentration of A and B nitrogen-containing defects in the diamonds using known times of annealing in the mantle. A new, two-stage thermal annealing model is presented that better constrains the thermal history of the diamond and that of the mantle lithosphere in which the diamond resided. The effect of heterogeneity within the analysed FTIR volume is quantitatively assessed and errors in model temperatures that can be introduced by studying whole diamonds instead of thin plates are discussed. The kinetics of platelet growth and degradation will be discussed and the potential for two separate, kinetically-controlled defect reactions to be used to constrain a full thermal history of the diamond will be assessed. [1] Kohn, S.C., Speich, L., Smith, C.B. and Bulanova, G.P., 2016. FTIR thermochronometry of natural diamonds: A closer look.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 16438 Abstract
Africa, Zimbabwe, Australia, South America, Brazil
Deposit - Murowa, Argyle, Machado River
Abstract: Fourier Transform Infrared (FTIR) spectroscopy is a commonly-used technique for investigating diamonds. It gives the most useful information if spatially-resolved measurements are used [1]. In this contribution we discuss the best way to acquire and present FTIR data from diamonds, using examples from Murowa (Zimbabwe), Argyle (Australia) and Machado River (Brazil). Examples of FTIR core-to-rim line scans, maps with high spatial resolution and maps with high spectral resolution that are fitted to extract the spatial variation of different nitrogen and hydrogen defects are presented. Model mantle residence temperatures are calculated from the concentration of A and B nitrogen-containing defects in the diamonds using known times of annealing in the mantle. A new, two-stage thermal annealing model is presented that better constrains the thermal history of the diamond and that of the mantle lithosphere in which the diamond resided. The effect of heterogeneity within the analysed FTIR volume is quantitatively assessed and errors in model temperatures that can be introduced by studying whole diamonds instead of thin plates are discussed. The kinetics of platelet growth and degradation will be discussed and the potential for two separate, kinetically-controlled defect reactions to be used to constrain a full thermal history of the diamond will be assessed. [1] Kohn, S.C., Speich, L., Smith, C.B. and Bulanova, G.P., 2016. FTIR thermochronometry of natural diamonds: A closer look.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 220 Abstract
Russia, Archangel, Kola Peninsula
Deposit - Grib
Abstract: Kimberlite is a composite rock that contains juvenile magmatic material and xenoliths of crustal and mantle rocks, including metasomatically reworked rocks and megacrysts. In spite of nearly 40-50 years of continuous study of kimberlites and SCLM, some aspects of their origin remain controversial. In particular, it is unclear yet whether the megacrysts are magmatic or metasomatic in origin and how they are related to kimberlite magmas. In this contribution, we compare the major (EMPA) and trace element (SIMS, LA-ICP-MS) compositions of clinopyroxene megacrysts from the Grib kimberlite (Arkhangelsk province, Russia) with clinopyroxenes from metasomatic clinopyroxene-phlogopite xenoliths and garnet peridotite xenoliths. The Grib kimberlite (376±3 Ma, Larionova et al., 2016) is located in the central part of the Arkhangelsk province (the northern part of the East European craton) in the Chernoozero kimberlite field. The geochemical composition of the kimberlites is similar to widespread South Africa group I kimberlites . The Grib kimberlite is well known for hosting a variety of mantle xenoliths, e.g., garnet peridotite, sheared peridotite, eclogite, metasomatised mantle material, as well as megacrysts of clinopyroxene, garnet, olivine, phlogopite, and ilmenite. The clinopyroxene megacrysts occur as rounded or angular grains up to 2 cm in size. They are usually surrounded by ultrafine kimberlite rim. The xenoliths of the metasomatic clinopyroxene-phlogopite rocks reach up to 6 cm in size and have a granoblastic texture. They consist of clinopyroxene (55 vol. %), phlogopite (45 vol. %) and minor calcite, barite, perovskite. Some clinopyroxene grains contain inclusion of relict olivine that is similar in composition to olivine from mantle-derived peridotite xenoliths within the Grib kimberlite (Sazonova et al., 2015). This suggests that these xenoliths could be formed by metasomatic reworking of SCLM peridotites. The megacryst clinopyroxene is compositionally similar to the clinopyroxene found in metasomatic xenoliths and corresponds to diopside. As compared to the typical clinopyroxene megacrysts worldwide, it has higher Mg# (>0.92), Cr# (0.21-0.62) and Ca# values (0.47-0.49) and lower Ti (659-1966 ppm) composition. The clinopyroxenes have (La/Sm)CI values from 0.58 to 1.57, and trace element patterns with deep negative Ti and shallow negative Zr-Hf anomalies. The major and trace-element compositions of these clinopyroxenes are very close to those of clinopyroxenes from garnet peridotite xenoliths in the Grib pipe (Kargin et al., 2016) that could be formed during the ascent and interaction of kimberlite mamas with a surrounding lithospheric mantle after crystallization of garnet and ilmenite megacrysts. Calculations showed that metasomatic agents in equilibrium with clinopyroxene megacrysts are similar in composition to kimberlite, which is consistent with proposed model. To sum up, we suggest that the formation of clinopyroxenes of megacrysts and mantle-derived clinopyroxene-phlogopite metasomatic xenoliths from the Grib kimberlite was related to the late-stage metasomatic reworking of SCLM by kimberlite magmas.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 16340 Abstract
South America, Brazil
Deposit - Juina
Abstract: We describe a new methodology to collect energy domain Mössbauer spectra of inclusions in natural diamonds using a Synchrotron Mössbauer Source (SMS). Measurements were carried out at the Nuclear Resonance beamline ID18 at the European Synchrotron Radiation Facility (Grenoble, France). We applied this non-destructive approach to collect SMS spectra of a ferropericlase inclusion still contained within its diamond host from Juina (Brazil). The high spatial resolution of the measurement (~ 15 ?m) enabled multiple regions of the 190 × 105 ?m2 inclusion to be sampled and showed that while Fe3 +/Fetot values in ferropericlase were below the detection limit (0.02) overall, there was a magnetic component whose abundance varied systematically across the inclusion. Hyperfine parameters of the magnetic component are consistent with magnesioferrite, and the absence of superparamagnetism allows the minimum particle size to be estimated as ~ 30 nm. Bulk Fe3 +/Fetot values are similar to those reported for other ferropericlase inclusions from Juina, and their variation across the inclusion can provide constraints on its history.
Abstract: The paper presents data on the composition of olivine macrocrysts from two Devonian kimberlite pipes in the Arkhangelsk diamond province: the Grib pipe (whose kimberlite belongs to type I) and Pionerskaya pipe (whose kimberlite is of type II, i.e., orangeite). The dominant olivine macrocrysts in kimberlites from the two pipes significantly differ in geochemical and isotopic parameters. Olivine macrocrysts in kimberlite from the Grib pipe are dominated by magnesian (Mg# = 0.92-0.93), Ti-poor (Ti < 70 ppm) olivine possessing low Ti/Na (0.05-0.23), Zr/Nb (0.28-0.80), and Zn/Cu (3-20) ratios and low Li concentrations (1.2-2.0 ppm), and the oxygen isotopic composition of this olivine ?18O = 5.64‰ is higher than that of olivine in mantle peridotites (?18O = 5.18 ± 0.28‰). Olivine macrocrysts in kimberlite from the Pionerskaya pipe are dominated by varieties with broadly varying Mg# = 0.90-0.93, high Ti concentrations (100-300 ppm), high ratios Ti/Na (0.90-2.39), Zr/Nb (0.31-1.96), and Zn/Cu (12-56), elevated Li concentrations (1.9-3.4 ppm), and oxygen isotopic composition ?18O = 5.34‰ corresponding to that of olivine in mantle peridotites. The geochemical and isotopic traits of low-Ti olivine macrocrysts from the Grib pipe are interpreted as evidence that the olivine interacted with carbonate-rich melts/fluids. This conclusion is consistent with the geochemical parameters of model melt in equilibrium with the low-Ti olivine that are similar to those of deep carbonatite melts. Our calculations indicate that the variations in the ?18O of the olivine relative the “mantle range” (toward both higher and lower values) can be fairly significant: from 4 to 7‰ depending on the composition of the carbonate fluid. These variations were formed at interaction with carbonate fluid, whose ?18O values do not extend outside the range typical of mantle carbonates. The geochemical parameters of high-Ti olivine macrocrysts from the Grib pipe suggest that their origin was controlled by the silicate (water-silicate) component. This olivine is characterized by a zoned Ti distribution, with the configuration of this distribution between the cores of the crystals and their outer zones showing that the zoning of the cores and outer zones is independent and was produced during two episodes of reaction interaction between the olivine and melt/fluid. The younger episode (when the outer zone was formed) likely involved interaction with kimberlite melt. The transformation of the composition of the cores during the older episode may have been of metasomatic nature, as follows from the fact that the composition varies from grain to grain. The metasomatic episode most likely occurred shortly before the kimberlite melt was emplaced and was related to the partial melting of pyroxenite source material.
Abstract: The paper presents data on the composition of olivine macrocrysts from two Devonian kimberlite pipes in the Arkhangelsk diamond province: the Grib pipe (whose kimberlite belongs to type I) and Pionerskaya pipe (whose kimberlite is of type II, i.e., orangeite). The dominant olivine macrocrysts in kimberlites from the two pipes significantly differ in geochemical and isotopic parameters. Olivine macrocrysts in kimberlite from the Grib pipe are dominated by magnesian (Mg# = 0.92-0.93), Ti-poor (Ti < 70 ppm) olivine possessing low Ti/Na (0.05-0.23), Zr/Nb (0.28-0.80), and Zn/Cu (3-20) ratios and low Li concentrations (1.2-2.0 ppm), and the oxygen isotopic composition of this olivine ?18O = 5.64‰ is higher than that of olivine in mantle peridotites (?18O = 5.18 ± 0.28‰). Olivine macrocrysts in kimberlite from the Pionerskaya pipe are dominated by varieties with broadly varying Mg# = 0.90-0.93, high Ti concentrations (100-300 ppm), high ratios Ti/Na (0.90-2.39), Zr/Nb (0.31-1.96), and Zn/Cu (12-56), elevated Li concentrations (1.9-3.4 ppm), and oxygen isotopic composition ?18O = 5.34‰ corresponding to that of olivine in mantle peridotites. The geochemical and isotopic traits of low-Ti olivine macrocrysts from the Grib pipe are interpreted as evidence that the olivine interacted with carbonate-rich melts/fluids. This conclusion is consistent with the geochemical parameters of model melt in equilibrium with the low-Ti olivine that are similar to those of deep carbonatite melts. Our calculations indicate that the variations in the ?18O of the olivine relative the “mantle range” (toward both higher and lower values) can be fairly significant: from 4 to 7‰ depending on the composition of the carbonate fluid. These variations were formed at interaction with carbonate fluid, whose ?18O values do not extend outside the range typical of mantle carbonates. The geochemical parameters of high-Ti olivine macrocrysts from the Grib pipe suggest that their origin was controlled by the silicate (water-silicate) component. This olivine is characterized by a zoned Ti distribution, with the configuration of this distribution between the cores of the crystals and their outer zones showing that the zoning of the cores and outer zones is independent and was produced during two episodes of reaction interaction between the olivine and melt/fluid. The younger episode (when the outer zone was formed) likely involved interaction with kimberlite melt. The transformation of the composition of the cores during the older episode may have been of metasomatic nature, as follows from the fact that the composition varies from grain to grain. The metasomatic episode most likely occurred shortly before the kimberlite melt was emplaced and was related to the partial melting of pyroxenite source material.
Geochimica et Cosmochimica Acta, Vol. 206, pp. 312-342.
Europe, Finland
Deposit - Lahtojoki
Abstract: A collection of 61 xenocrystic and 12 eclogite xenolith-derived diamonds from the 600 Ma Lahtojoki kimberlite in central Finland has been investigated. Calculated pressure and temperature conditions for the diamondiferous eclogites are in excess of 5.5 GPa and 1300 °C, suggesting residence depths greater than 180 km, near the base of the Karelian cratonic mantle lithosphere. Geochemically, the eclogite xenoliths have gabbroic compositions showing positive Eu and Sr anomalies, relatively low ?REE and elevated Al2O3 contents, yet garnets have ambiguous ?18O values of 5.7‰ and 5.9‰. Gabbroic eclogite formation could therefore be linked to either subduction processes during the 1.9 Ga Svecofennian orogeny or to cumulate processes during 2.1 Ga rift-induced magmatism. Determination of the oxygen fugacity of Lahtojoki eclogite xenoliths from both this work and previous studies suggests that diamond-bearing eclogites may be more reduced (?FMQ-3.5) compared to barren eclogites (?FMQ-1.7). While recycled oceanic crust protoliths for the eclogites remain a possibility, the carbon isotopic compositions and nitrogen abundances of the Lahtojoki diamonds indicate mantle-derived volatile sources. All diamonds (i.e., loose and eclogite xenolith-derived) display a restricted range of ?13C values from ?7.8‰ to ?3.7‰ that overlaps with the carbon isotopic composition of Earth’s mantle. The Lahtojoki diamond ?13C values form a negatively skewed distribution, indicating diamond growth from reduced mantle-derived carbon sources such as methane- (CH4) bearing fluids. Nitrogen contents of the Lahtojoki diamonds range from 40 to 1830 atomic ppm with a mean of ?670 atomic ppm; these elevated nitrogen contents combined with the close association to eclogites suggest an eclogitic or crustal volatile source. However, the Karelian craton was periodically intruded by ultramafic alkaline magmas since at least 1.8 Ga, noting in particular the occurrence of phlogopite-rich kimberlites and olivine lamproites between 1200 and 700 Ma. We argue that this punctuated volatile-rich magmatism simultaneously metasomatised the cratonic mantle lithosphere, forming nitrogen enriched phlogopite-bearing metasomes. We propose that reduced, carbon-bearing and nitrogen-rich fluids were remobilized to form the Lahtojoki diamonds. The diamond-forming event(s) most probably occurred during or shortly prior to the entraining kimberlite magmatism as indicated by the diamond nitrogen aggregation systematics. Involvement of reduced diamond-forming fluids is supported by both the negative skewness of Lahtojoki diamond ?13C values and the more reduced nature of the diamondiferous Lahtojoki eclogites compared with their more oxidized barren counterparts. Our results from the diamondiferous eclogites derived from the deepest parts of the Karelian cratonic mantle root are in support of methane being the stable carbon volatile species at the base of thick continental lithosphere.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 9187 Abstract
Africa, Zimbabwe, Sierra Leone
Deposit - Marange, Zimmi
Abstract: Traditional models for diamond formation within the lithospheric mantle invoke either carbonate reduction or methane oxidation. Both these mechanisms require some oxygen exchange with the surrounding wall-rock at the site of diamond precipitation. However, peridotite does not have sufficient buffering capacity to allow for diamond formation via these traditional models and instead peridotitic diamonds may form through isochemical cooling of H 2 O-rich CHO fluids [1]. Marange mixed-habit diamonds from eastern Zimbabwe provide the first natural confirmation of this new diamond growth model [2]. Although Marange diamonds do not contain any silicate or sulphide inclusions, they contain Ni-N-vacancy complexes detected through photoluminescence (PL) spectroscopy that suggest the source fluids equilibrated in the Ni-rich depleted peridotitic lithosphere. Cuboid sectors also contain abundant micro-inclusions of CH 4 , the first direct observation of reduced CH 4-rich fluids that are thought to percolate through the lithospheric mantle [2]. In fluid inclusion-free diamonds, core-to-rim trends in ? 13 C and N content are used to infer the speciation of the diamond-forming fluid. Core to rim trends of increasing ? 13 C with decreasing N content are interpreted as diamond growth from oxidized CO 2-or carbonate-bearing fluids. Diamond growth from reduced species should show the opposite trends-decreasing ? 13 C from core to rim with decreasing N content. Within the CH 4-bearing growth sectors of Marange diamonds, however, such a 'reduced' trend is not observed. Rather, ? 13 C increases from core to rim within a homogeneously grown zone [2]. These contradictory observations can be explained through either mixing between CH 4-and CO 2-rich end-members of hydrous fluids [2] or through closed system precipitation from an already mixed CH 4-CO 2 H 2 O-maximum fluid with XCO 2 (CO 2 /[CO 2 +CH 4 ]) between 0.3 and 0.7 [3]. These results demonstrate that Marange diamonds precipitated from cooling CH 4-CO 2-bearing hydrous fluids rather than through redox buffering. As this growth mechanism applies to both the fluid-rich cuboid and gem-like octahedral sectors of Marange diamonds, a non-redox model for diamond formation from mixed CH 4-CO 2 fluids is indicated for a wider range of gem-quality peridotitic diamonds. Indeed, at the redox conditions of global diamond-bearing lithospheric mantle (FMQ-2 to-4; [4]), CHO fluids are strongly water-dominated and contain both CH 4 and CO 2 as dominant carbon species [5]. By contrast diamond formation in eclogitic assemblages, through either redox buffering or cooling of carbon-bearing fluids, is not as well constrained. Zimmi diamonds from the West African craton have eclogitic sulphide inclusions (with low Ni and high Re/Os) and formed at 650 Ma, overlapping with the timing of subduction [6]. In one Zimmi diamond, a core to rim trend of decreasing ? 13 C (-23.4 to-24.5 %¸) and N content is indicative of formation from reduced C 2 H 6 /CH 4-rich fluids, likely derived from oceanic crust recycled during Neoproterozoic subduction. Unlike mixed CH 4-CO 2 fluids near the water maximum, isochemical cooling or ascent of such reduced CHO fluids is not effficient at diamond precipitation. Furthermore, measurable carbon isotopic variations in diamond are not predicted in this model and therefore cannot be reconciled with the ?1 internal variation seen. Consequently, this Zimmi eclogitic diamond likely formed through redox buffering of reduced subduction-related fluids, infiltrating into sulphide-bearing eclogite.
Geochimica et Cosmochimica Acta, in press available 55p.
Africa, South Africa
Deposit - Roberts Victor
Abstract: Heterogeneous, modally banded kyanite-bearing and bimineralic eclogites from the lithospheric mantle, collected at the Roberts Victor Diamond mine (South Africa), show a reaction texture in which kyanite is consumed. Geothermobarometric calculations using measured mineral compositions in Perple_X allowed the construction of a P-T path showing a steep, cool prograde metamorphic gradient of 2 °C/km to reach peak conditions of 5.8 GPa and 890 °C for the kyanite eclogite. The kyanite-out reaction formed bimineralic eclogite and is probably an integral part of the mineralogical evolution of most archetypal bimineralic eclogites at Roberts Victor and potentially elsewhere. The kyanite-out reaction occured at close to peak pressure (5.3 GPa) and was associated with a rise in temperature to 1380 °C. Mass balance calculations show that upon breakdown, the kyanite component is fully accommodated in garnet and omphacite via a reaction system with low water fugacity that required restricted fluid influx from metasomatic sources. The ?18O values of garnets are consistently higher than normal mantle values. Each sample has its characteristic trend of ?18O variance between garnets in the kyanite-bearing sections and those in the bimineralic parts covering a range between 5.1‰ and 6.8‰. No systematic change in O-isotope signature exists across the sample population. Differences in garnet trace element signatures between differing lithologies in the eclogites are significant. Grossular-rich garnets coexisting with kyanite have strong positive Eu-anomalies and low Gd/Yb ratios, while more pyrope-rich garnets in the bimineralic sections have lost their positive Eu-anomaly, have higher Gd/Yb ratios and generally higher heavy rare earth element contents. Garnets in the original kyanite-bearing portions thus reflect the provenance of the rocks as metamorphosed gabbros/troctolites. The kyanite-out reaction was most likely triggered by a heating event in the subcratonic lithosphere. As kyanite contains around 100 ppm of H2O it is suggested that the kyanite-out reaction, once initiated by heating and restricted metasomatic influx, was promoted by the release of water contained in the kyanite. The steep (high-P low-T) prograde P-T path defining rapid compression at low heating rates is atypical for subduction transport of eclogites into the lithospheric mantle. Such a trajectory is best explained in a model where strong lateral compression forces eclogites downward to higher pressures, supporting models of cratonic lithosphere formation by lateral collision and compression.
van den Heuvel, Q., Matveev, S., Drury, M., Gress, M., Chinn, I., Davies, G.
Genesis of diamond inclusions: an integrated cathodluminescence ( CL) and electron backscatter diffraction (EBSD) study on eclogitic and peridotitic inclusions and their diamond host.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 6564 Abstract
van den Heuvel, Q., Matveev, S., Drury, M., Gress, M., Chinn, I., Davies, G.
Genesis of diamond inclusions: an integrated cathodluminescence ( CL) and electron backscatter diffraction (EBSD) study on eclogitic and peridotitic inclusions and their diamond host.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 6564 Abstract
Abstract: Moore proposes in his Comment (Moore, 2017) that marginal zones in olivine grains in kimberlites (Fig. 1a) are produced by crystallization from kimberlite melt. He suggests that the chemical zones observed in these marginal zones (inner transition zones and outer margins, illustrated in his fig. 1) result from abrupt changes in distribution coefficients during crystallization. He proposes that the transition zones, characterized by variable Fo at constant and high Ni contents, are produced by crystallization with high KdFe-Mg (= 0•45) and low DNi (= 4) whereas the margins, characterized by a sharp drop in Ni content at nearly constant Fo (Fig. 1b), are produced by crystallization with higher DNi owing to a sudden change in physical conditions of crystallization (P,…
Abstract: Casper College undergraduate students investigated the feasibility of finding hidden kimberlite pipes by means of geological mapping, geophysics, and stream sediment sampling. The Precambrian Laramie Mountains of southeastern Wyoming, locally known as the Iron Mountain Kimberlite district, was chosen based on previous work conducted by the Wyoming State Geological Survey (WSGS), geology of the region, and known kimberlite pipes. Data was collected using micro gravimeter - Scintrex CG-5, magnetometer - G-858 MagMapper, and electrical resistivity - SuperSting R8/IP/SP. Target one was chosen while pre-mapping the area and a topographic bowl like depression was identified. Micro gravimeter data was collected on a 56m transect at 8m intervals. Magnetometer data was collected in an area of 122m by 92m running in a 8m parallel array. Electrical resistivity was collected along a 56m transect at 8m intervals. Target two was chosen because the WSGS identified a regional magnetic anomaly and follow-up research was needed. Microgravimeter data was collected on a 56m transect at 8m intervals. Magnetometer data was collected from an area of 122m by 92m running in an 8m parallel array. Electrical resistivity was collected along a 56m transect at 8m intervals. Two drill site locations were selected based on the geophysical results to prove kimberlite is present at depth. Sediment samples were taken along Middle Sybille Creek and yielded a variety of pink to very deep red and purple colored garnets which have been sent in for EPMA (electron probe micro analyses) testing to determine the garnet-spinel compositions. Once complete the geochemical analyses will help determine if either target has a greater potential to be a diamondiferous kimberlite pipe.
Abstract: The paper presents new petrographic, major element and Fourier transform infrared (FTIR) spectroscopy data and PT-estimates of whole-rock samples and minerals of a collection of 19 relatively fresh peridotite xenoliths from the Udachnaya kimberlite pipe, which were recovered from its deeper levels. The xenoliths are non-deformed (granular), medium-deformed and highly deformed (porphyroclastic, mosaic-porphyroclastic, mylonitic) lherzolites, harzburgite and dunite. The lherzolites yielded equilibration temperatures (T) and pressures (P) ranging from 913 to 1324 °C and from 4.6 to 6.3 GPa, respectively. The non-deformed and medium-deformed peridotites match the 35 mW/m2 conductive continental geotherm, whereas the highly deformed varieties match the 45 mW/m2 geotherm. The content of water spans 2 ± 1-95 ± 52 ppm in olivine, 1 ± 0.5-61 ± 9 ppm in orthopyroxene, and 7 ± 2-71 ± 30 ppm in clinopyroxene. The amount of water in garnets is negligible. Based on the modal proportions of mineral phases in the xenoliths, the water contents in peridotites were estimated to vary over a wide range from < 1 to 64 ppm. The amount of water in the mantle xenoliths is well correlated with the deformation degree: highly deformed peridotites show highest water contents (64 ppm) and those medium-deformed and non-deformed contain ca. 1 ppm of H2O. The high water contents in the deformed peridotites could be linked to metasomatism of relatively dry diamondiferous cratonic roots by hydrous and carbonatitic agents (fluids/melts), which may cause hydration and carbonation of peridotite and oxidation and dissolution of diamonds. The heterogeneous distribution of water in the cratonic mantle beneath the Udachnaya pipe is consistent with the models of mantle plume or veined mantle structures proposed based on a trace element study of similar xenolithic suits. Mantle metasomatism beneath the Siberian Craton and its triggered kimberlite magmatism could be induced by mantle enrichment in volatiles (H2O, CO2) supplied by numerous subduction zones which surrounded the Siberian continent in Neoproterozoic-Cambrian time.
Abstract: The Lake Tamiskaming Kimberlite Field, in Ontario, Canada is host to multiple kimberlite pipes, such as the KRVY Kimberlite Pipe, south of Latchford, Ontario. Drill core of this kimberlite pipe, collected by Temex Resources Corporation, confirmed the diamondiferous nature, with microdiamonds being retrieved. Thin sections of the drill core samples suggest the pipe is highly altered through serpentinization. Euhedral to subhedral grains of mica, such as phlogopite and biotite, compose the phenocryst and matrix components of the samples. Electron microprobe analysis will be used to determine the composition of the micas, in order to constrain the origin conditions of these grains, determining if the grains originate from crustal or magmatic components. Micro X-ray Diffraction will determine the mineralogy in the samples. Other likely xenocrystic minerals include quartz, etc. Textural and compositional attributes of the KRVY Kimberlite will be compared to data collected from the approximately twelve known kimberlite pipes within 25 kilometres (15.5 miles) of the specified kimberlite in order to find similarities or patterns. Geochemical analysis will better constrain the formation conditions of this pipe and allow comparison with other surrounding pipes in the Lake Tamiskaming Kimberlite Field.
deposit - Taughannock Creek, Ithica, Dewitt Reservoir
Abstract: Kimberlites are unusual igneous rocks that are not only the singular source of gem quality diamonds, but also a source of upper mantle and lower crustal material for scientific study. As kimberlite magmas rise, they disaggregate xenoliths from the surrounding country rocks. One mineral that is commonly picked up and transported to the surface is garnet, and their compositions have been correlated with different mantle conditions and source materials. The goal of our study is to use garnet compositions to characterize the diversity of lithologies sampled by Mesozoic kimberlitic intrusions in New York State. Approximately 90 kimberlitic dikes cut through the Paleozoic sedimentary rocks of central New York State, most clustered around the cities of Ithaca and Syracuse. Samples of garnet-bearing kimberlites were collected from both of these localities (Taughannock Creek, Ithaca and Dewitt Reservoir, Syracuse), in order to compare the garnet populations present to see if the two dikes sampled similar mantle and crustal materials. Garnets were extracted from both dikes, and their bulk compositions were obtained using energy-dispersive, x-ray spectrometry (SEM-EDS). We were able to identify four major compositional groups of garnets: 1) low to moderate Cr pyrope, 2) high Cr pyrope, 3) almandine, and 4) grossular. Samples of each of these were then analyzed for trace element composition by laser ablation, inductively coupled plasma, mass spectrometry (LA-ICP-MS).
Both dikes contain macrocrysts of almandine and Cr-bearing pyrope (up to ~ 5 wt. % Cr2O3); garnets with a high grossular component were only found in the Dewitt kimberlite. Based on the classification of Gurney et al. (1984), none of the garnets indicate a high diamond potential for either kimberlite. While the pyrope and almandine macrocrysts in both dikes are broadly similar in composition, sub-populations of garnets can be recognized based on trace element profiles. Preliminary analysis of the data suggests that the kimberlite intrusions in central New York sampled garnets from a heterogeneous mantle source and, in addition, sampled garnets from a Grenvillian lower crust.
Russia, Kola Peninsula, Europe, Finland, Canada, British Columbia
deposit - Khibina, Fir, Siilinjarvi
Abstract: Phosphorus is the central ingredient in fertilizer that allows modern agriculture to feed the world’s population. This element, also critical in a host of industrial applications, is a nonrenewable resource that is sourced primarily from the phosphatic mineral apatite, hosted in sedimentary and igneous ores. World phosphate resources are estimated by the U.S. Geological Survey at ca. 300,000 Mt, of which 95% are sedimentary and 5% are igneous. Current known USGS reserve estimates are sufficient for a maximum of 200 to 300 years; the exploration and discovery of new resources, enhanced mining technologies, and new technologies aimed at the recovery and recycling of P from sewage and agricultural runoff will all contribute to extending P production. Igneous ores are generally associated with Phanerozoic carbonatites and silica-deficient alkalic intrusions that typically average 5 to 15 wt % P2O5, which can be beneficiated to high-grade concentrates of at least 30 wt % P2O5 with few contaminants. Carbonatites are typically the smallest and youngest parts of a carbonatite-alkaline rock complex that formed during fractional crystallization of a calcic parental alkaline silicate melt, or from liquid immiscibility of a carbonate-rich nephelinite that underwent magmatic fractionation and differentiation during ascent from the mantle source. Fluorapatite generally crystallizes early, near the liquidus, and over a small temperature interval below the apatite saturation temperature that varies strongly with temperature, SiO2 and CaO concentrations, and the aluminosity of the melt. Carbonatite-alkaline rock complexes commonly possess a concentric, zonal structure thought to reflect caldera volcanism. Pathfinder elements in soils, sediments, tills, and vegetation include Nb, rare earth elements (REEs), P, Ba, Sr, F, U, and Th, and in water, F, Th, and U are indicators. Remote sensing techniques with the ability to identify minerals rich in CO3, REEs, and Fe2+ that are characteristic of carbonatites are also important exploration tools that may provide vectors to ore. Sedimentary phosphorite is a marine bioelemental sedimentary rock that contains >18 wt % P2O5. While small peritidal phosphorites formed in Precambrian coastal environments, economically significant upwelling-related phosphorite did not accumulate until the late Neoproterozoic and continued through the Phanerozoic. Coastal upwelling delivered deep, P-rich waters to continental shelves and in epeiric seas to drive phosphogenesis and form the largest phosphorites on Earth. High-grade deposits formed as a result of hydraulic concentration of phosphate grains to form granular beds with minimal gangue. The amalgamation of these beds into decameter-thick, stratiform ore zones is generally focused along the maximum flooding surface, which is a primary exploration target in upwelling-related phosphorite. In addition to P, other elements concentrated in igneous and sedimentary phosphorites are Se, Mo, Zn, Cu, and Cr, which are important agricultural micronutrients. Other saleable by-products include U and REEs. The U concentration in sedimentary phosphorite is generally between 50 and 200 ppm, but can be as high as 3,000 ppm, making it an increasingly important source of U for the nuclear industry. The concentration of REEs in some sedimentary phosphorites is comparable to the world’s richest igneous and Chinese clay-type REE deposits. The source of the dissolved P in upwelling ocean water is ultimately derived from the chemical weathering of continental rocks, the process that links igneous and sedimentary phosphorites through time and space. The covarying temporal relationship of igneous and sedimentary deposits suggests that plate tectonics and the concentration of apatite in a progressively more felsic crust underpins the feedback processes regulating the biogeochemical cycling of P. Critical to the generation of greenfield exploration targets is the recognition that large P deposits emerged in the late Neoproterozoic. The geological environments conducive for exploration can be constrained from an understanding of ore-forming processes by the use of complementary petrological techniques, including fieldwork, petrography, sedimentology, sequence stratigraphy, and geochemistry.
Russia, Kola Peninsula, Europe, Finland, Canada, British Columbia
deposit - Khibina, Fir, Siilinjarvi
Abstract: Phosphorus is the central ingredient in fertilizer that allows modern agriculture to feed the world’s population. This element, also critical in a host of industrial applications, is a nonrenewable resource that is sourced primarily from the phosphatic mineral apatite, hosted in sedimentary and igneous ores. World phosphate resources are estimated by the U.S. Geological Survey at ca. 300,000 Mt, of which 95% are sedimentary and 5% are igneous. Current known USGS reserve estimates are sufficient for a maximum of 200 to 300 years; the exploration and discovery of new resources, enhanced mining technologies, and new technologies aimed at the recovery and recycling of P from sewage and agricultural runoff will all contribute to extending P production. Igneous ores are generally associated with Phanerozoic carbonatites and silica-deficient alkalic intrusions that typically average 5 to 15 wt % P2O5, which can be beneficiated to high-grade concentrates of at least 30 wt % P2O5 with few contaminants. Carbonatites are typically the smallest and youngest parts of a carbonatite-alkaline rock complex that formed during fractional crystallization of a calcic parental alkaline silicate melt, or from liquid immiscibility of a carbonate-rich nephelinite that underwent magmatic fractionation and differentiation during ascent from the mantle source. Fluorapatite generally crystallizes early, near the liquidus, and over a small temperature interval below the apatite saturation temperature that varies strongly with temperature, SiO2 and CaO concentrations, and the aluminosity of the melt. Carbonatite-alkaline rock complexes commonly possess a concentric, zonal structure thought to reflect caldera volcanism. Pathfinder elements in soils, sediments, tills, and vegetation include Nb, rare earth elements (REEs), P, Ba, Sr, F, U, and Th, and in water, F, Th, and U are indicators. Remote sensing techniques with the ability to identify minerals rich in CO3, REEs, and Fe2+ that are characteristic of carbonatites are also important exploration tools that may provide vectors to ore. Sedimentary phosphorite is a marine bioelemental sedimentary rock that contains >18 wt % P2O5. While small peritidal phosphorites formed in Precambrian coastal environments, economically significant upwelling-related phosphorite did not accumulate until the late Neoproterozoic and continued through the Phanerozoic. Coastal upwelling delivered deep, P-rich waters to continental shelves and in epeiric seas to drive phosphogenesis and form the largest phosphorites on Earth. High-grade deposits formed as a result of hydraulic concentration of phosphate grains to form granular beds with minimal gangue. The amalgamation of these beds into decameter-thick, stratiform ore zones is generally focused along the maximum flooding surface, which is a primary exploration target in upwelling-related phosphorite. In addition to P, other elements concentrated in igneous and sedimentary phosphorites are Se, Mo, Zn, Cu, and Cr, which are important agricultural micronutrients. Other saleable by-products include U and REEs. The U concentration in sedimentary phosphorite is generally between 50 and 200 ppm, but can be as high as 3,000 ppm, making it an increasingly important source of U for the nuclear industry. The concentration of REEs in some sedimentary phosphorites is comparable to the world’s richest igneous and Chinese clay-type REE deposits. The source of the dissolved P in upwelling ocean water is ultimately derived from the chemical weathering of continental rocks, the process that links igneous and sedimentary phosphorites through time and space. The covarying temporal relationship of igneous and sedimentary deposits suggests that plate tectonics and the concentration of apatite in a progressively more felsic crust underpins the feedback processes regulating the biogeochemical cycling of P. Critical to the generation of greenfield exploration targets is the recognition that large P deposits emerged in the late Neoproterozoic. The geological environments conducive for exploration can be constrained from an understanding of ore-forming processes by the use of complementary petrological techniques, including fieldwork, petrography, sedimentology, sequence stratigraphy, and geochemistry.
Russia, Kola Peninsula, Europe, Finland, Canada, British Columbia
deposit - Khibina, Fir, Siilinjarvi
Abstract: Phosphorus is the central ingredient in fertilizer that allows modern agriculture to feed the world’s population. This element, also critical in a host of industrial applications, is a nonrenewable resource that is sourced primarily from the phosphatic mineral apatite, hosted in sedimentary and igneous ores. World phosphate resources are estimated by the U.S. Geological Survey at ca. 300,000 Mt, of which 95% are sedimentary and 5% are igneous. Current known USGS reserve estimates are sufficient for a maximum of 200 to 300 years; the exploration and discovery of new resources, enhanced mining technologies, and new technologies aimed at the recovery and recycling of P from sewage and agricultural runoff will all contribute to extending P production. Igneous ores are generally associated with Phanerozoic carbonatites and silica-deficient alkalic intrusions that typically average 5 to 15 wt % P2O5, which can be beneficiated to high-grade concentrates of at least 30 wt % P2O5 with few contaminants. Carbonatites are typically the smallest and youngest parts of a carbonatite-alkaline rock complex that formed during fractional crystallization of a calcic parental alkaline silicate melt, or from liquid immiscibility of a carbonate-rich nephelinite that underwent magmatic fractionation and differentiation during ascent from the mantle source. Fluorapatite generally crystallizes early, near the liquidus, and over a small temperature interval below the apatite saturation temperature that varies strongly with temperature, SiO2 and CaO concentrations, and the aluminosity of the melt. Carbonatite-alkaline rock complexes commonly possess a concentric, zonal structure thought to reflect caldera volcanism. Pathfinder elements in soils, sediments, tills, and vegetation include Nb, rare earth elements (REEs), P, Ba, Sr, F, U, and Th, and in water, F, Th, and U are indicators. Remote sensing techniques with the ability to identify minerals rich in CO3, REEs, and Fe2+ that are characteristic of carbonatites are also important exploration tools that may provide vectors to ore. Sedimentary phosphorite is a marine bioelemental sedimentary rock that contains >18 wt % P2O5. While small peritidal phosphorites formed in Precambrian coastal environments, economically significant upwelling-related phosphorite did not accumulate until the late Neoproterozoic and continued through the Phanerozoic. Coastal upwelling delivered deep, P-rich waters to continental shelves and in epeiric seas to drive phosphogenesis and form the largest phosphorites on Earth. High-grade deposits formed as a result of hydraulic concentration of phosphate grains to form granular beds with minimal gangue. The amalgamation of these beds into decameter-thick, stratiform ore zones is generally focused along the maximum flooding surface, which is a primary exploration target in upwelling-related phosphorite. In addition to P, other elements concentrated in igneous and sedimentary phosphorites are Se, Mo, Zn, Cu, and Cr, which are important agricultural micronutrients. Other saleable by-products include U and REEs. The U concentration in sedimentary phosphorite is generally between 50 and 200 ppm, but can be as high as 3,000 ppm, making it an increasingly important source of U for the nuclear industry. The concentration of REEs in some sedimentary phosphorites is comparable to the world’s richest igneous and Chinese clay-type REE deposits. The source of the dissolved P in upwelling ocean water is ultimately derived from the chemical weathering of continental rocks, the process that links igneous and sedimentary phosphorites through time and space. The covarying temporal relationship of igneous and sedimentary deposits suggests that plate tectonics and the concentration of apatite in a progressively more felsic crust underpins the feedback processes regulating the biogeochemical cycling of P. Critical to the generation of greenfield exploration targets is the recognition that large P deposits emerged in the late Neoproterozoic. The geological environments conducive for exploration can be constrained from an understanding of ore-forming processes by the use of complementary petrological techniques, including fieldwork, petrography, sedimentology, sequence stratigraphy, and geochemistry.
Neues Jahrbuch fur Mineralogie, Vol. 194, 2, pp. 165-173.
Russia, Kola Peninsula
deposit - Kovdor
Abstract: Isolueshite, a cubic complex oxide with the formula NaNbO3, occurs as euhedral crystals 0.4 - 0.7 mm in size in calcite carbonatite, Kovdor ultrabasic-alkaline complex (Kola, Russia). Average composition of isolueshite, based on 40 analyses by wavelength-dispersive electron microprobe is (Na0.84Ca0.07Sr0.01La0.01Ce0.01)?0.95(Nb0.90Ti0.11)?1.01O3. Minor and trace elements are Ti (4.1- 6.8 wt.% TiO2), REEs (1.8 - 4.0 wt.% REE2O3), Ca (1.7- 3.3 wt.% CaO), Zr (0.1- 0.8 wt.% ZrO2), Sr (0.3 - 0.4 wt.% SrO), Th (0.1- 0.5 wt.% ThO2), Fe (0.1- 0.2 wt.% Fe2O3) and Ta (0.1 wt.% Ta2O5). The crystal structure of isolueshite was refined to an agreement index (R1) of 0.028 for 82 unique reflections with |F0| ? 4 ?(F). The mineral is cubic, Pm3-m, a = 3.9045(5) Å and V = 59.525(13) Å3. The diffraction pattern of the crystal contains only regular and strong Bragg reflections with no signs of diffuse scattering. There are two sites in the crystal structure: A is 12-coordinated (A-O = 2.556(3) Å) and located at the corners of the cubic primitive cell and B is situated in the center of the unit-cell and has an octahedral coordination. The crystal-chemical formula based on the structure refinement is (Na0.84(1)Ca0.16(1))(Nb0.88(1)Ti0.12(1))O3. We suggest that isolueshite is a quenched (kinetically favored) polymorph of lueshite that formed as a result of rapid crystallization due to the sudden drop in temperature and/or pressure.
Abstract: Kimberlitic magmaclasts are discrete ovoid magmatic fragments that formed prior to emplacement from disrupted kimberlite magma. To provide new constraints on the origin and evolution of the kimberlite melts, we document the mineralogy and petrography of a magmaclast recovered from one of the ca. 520 Ma Venetia kimberlites, South Africa. The sample (BI9883) has a sub-spherical shape and consists of a ~ 10 mm diameter central olivine macrocryst, surrounded by porphyritic kimberlite. The kimberlitic material consists of concentrically aligned, altered olivine phenocrysts, set in a crystalline groundmass of calcite, chromite, perovskite, phlogopite, apatite, ilmenite, titanite, sulphides, rutile and magnetite along with abundant alteration phases (i.e. serpentine, talc and secondary calcite). These features are typical of archetypal hypabyssal kimberlites. We examined primary fluid/melt inclusions in chromite, perovskite and apatite containing a diversity of daughter phases. Chromite and perovskite host polycrystalline inclusions containing abundant alkali-carbonates (i.e. enriched in K, Na, Ba, Sr), phosphates, Na-K chlorides, sulphides and equal to lesser quantities of olivine, phlogopite and pleonaste. In contrast, apatite hosts polycrystalline assemblages with abundant alkali-carbonates and Na-K chlorides and lesser amounts of olivine, monticellite and phlogopite. Numerous solid inclusions of shortite (Na2Ca2(CO3)3), Na-Sr-carbonates and apatite occur in groundmass calcite along with fluid inclusions containing daughter crystals of Na-carbonates and Na-chlorides. The primary inclusions in chromite, perovskite and apatite are considered to represent remnants of fluid(s)/melt(s) trapped during crystallisation of the host minerals, whereas the fluid inclusions in calcite are probably secondary in origin. The component proportions of these primary fluid/melt inclusions were estimated in an effort to constrain the composition of the evolving kimberlite melt. These estimates suggest melt evolution from a silicate-carbonate kimberlite melt that became increasingly enriched in carbonates, phosphates, alkalis and chlorides, in response to the fractional crystallisation of constituent minerals (i.e. olivine to apatite). The concentric alignment of crystals around the olivine kernel and ovoid shape of the magmaclast can be ascribed to the low viscosity of the kimberlite melt and rapid rotation whilst in a liquid or partial crystalline state, or to progressive layer-by-layer growth of the magmaclast. Although the mineralogy of our sample is similar to hypabyssal kimberlites worldwide, it differs from hypabyssal kimberlite units in the main Venetia pipes, which contain monticellite-phlogopite rich assemblages and segregationary matrix textures. Therefore magmaclast BI9883 probably originated from a batch of magma distinct from those that produced known hypabyssal units within the Venetia kimberlite cluster.
Australian Journal of Earth Sciences, Vol. 64, 4, pp. 557-564.
Australia, New South Wales
deposit - Bingara
Abstract: A paleo-alluvial 0.21 ct yellow diamond (L058) from Bingara (NSW) has three inclusions of coesite (two subequant crystals and one thin plate), each under more than 3.1 GPa internal pressure as measured by Raman spectroscopy. These inclusions cause overlapping birefringent retardation stress/strain haloes in the host diamond, visible under cross-polarised light. The complicated retardation pattern is quantified by mapping targeted retardation contours (170 nm, 270 nm and 380 nm) onto a photo of the diamond. A mathematical model of retardation is developed for each inclusion, and then the combined light retardations (CLR) are calculated using radial and tangential components with spherical and elliptical geometries. The CLR model reproduces most features of the measured data, but remaining differences may be due to local release of stress/strain by two short fractures radiating from one inclusion.
South African Journal of Geology, Vol. 119, 4, pp. 585-606.
Africa, South Africa
deposit - Lichtenburg Ventersdorp
Abstract: Diamond-bearing gravels of the Lichtenburg-Ventersdorp area of the North West Province are associated with north-south orientated sinuous ‘runs’ that occur almost entirely on a flat erosional surface of the Malmani dolomites (Transvaal Supergroup) at some 1,500 m elevation. East to west, this dolomite plain measures 150 km, and north-south it is on average 40 km wide. This unconformity, which first developed before the Pretoria Group sedimentation over a period of at least 80 Myr, is marked by siliceous breccias (palaeo-karst infill) and conglomerates (reworked breccias). It was exhumed in pre-Karoo and post-Gondwana times. Glacial pavements and remnants of thin Lower Karoo sediments are also found on this polyphase surface. The gravels that make up these ‘runs’ and sinkholes directly or indirectly linked to these runs, are coarse-grained, very poorly-sorted, and are best described as diamictites. The ‘runs’ are narrow, elongated, generally positive ridges that meander across the dolomite surface and are up to 30 km long and between 80 to 300 m wide. They have always been regarded as post-Cretaceous drainage features linked to southward-flowing river systems. Diamonds were discovered in these ‘runs’ and they have produced some 12 million carats. However, no Cainozoic fossils or artefacts have ever been found in almost 90 years of mining. From new field evidence, geomorphological studies, age dating from inclusions in diamond and zircon and clay analyses, it is proposed that these coarse-grained runs represent proximal palaeoeskers of the last deglaciation of the Dwyka continental ice sheet, that are preserved on this ancient ‘palimpsest’ surface. The age of the deposit is constrained by two populations of agate within the diamictites that are linked to two separate volcanic units of the Pretoria Group. In addition, the youngest crustal zircon ages from the gravels are 1 Ba, but mantle zircons from Lichtenburg suggest that these have been derived from Cambrian age kimberlites. Analysis of inclusions in diamond support a Neoproterozoic to Cambrian source for the diamonds, so the absence of diamonds from Mesozoic kimberlites and Cainozoic fossils within the gravels support the conclusion that the runs are of Karoo age.
Abstract: New mineralogical and bulk-rock geochemical data for the recently recognised Mesoproterozoic (ca. 1100 Ma) and late Cretaceous (ca. 90 Ma) kimberlites in the Timmasamudram cluster (TKC) of the Wajrakarur kimberlite field (WKF), Eastern Dharwar Craton, southern India, are presented. On the basis of groundmass mineral chemistry (phlogopite, spinel, perovskite and clinopyroxene), bulk-rock chemistry (SiO2, K2O, low TiO2, Ba/Nb and La/Sm), and perovskite Nd isotopic compositions, the TK-1 (macrocrystic variety) and TK-4 (Macrocrystic variety) kimberlites in this cluster are here classified as orangeites (i.e. Group II kimberlites), with geochemical characteristics that are very similar to orangeites previously described from the Bastar Craton in central India, as well as the Kaapvaal Craton in South Africa. The remaining kimberlites (e.g., TK-2, TK-3 and the TK-1 microcrystic variant), are more similar to other 1100 Ma, Group I-type kimberlites of the Eastern Dharwar Craton, as well as the typical Group I kimberlites of the Kaapvaal Craton. Through the application of geochemical modelling, based on published carbonated peridotite/melt trace element partition coefficients, we show that the generation of the TKC kimberlites and the orangeites results from low degrees of partial melting of a metasomatised, carbonated peridotite. Depleted mantle (TDM) Nd perovskite model ages of the 1100 Ma Timmasamudram kimberlites show that the metasomatic enrichment of their source regions are broadly similar to that of the Mesoproterozoic kimberlites of the EDC. The younger, late Cretaceous (ca. 90 Ma) TK-1 (macrocrystic variant) and TK-4 kimberlites, as well as the orangeites from the Bastar Craton, share similar Nd model ages of 1100 Ma, consistent with a similarity in the timing of source enrichment during the amalgamation of Rodinia supercontinent. The presence of late Cretaceous diamondiferous orangeite activity, presumably related to the location of the Marion hotspot in southern India at the time, suggests that thick lithosphere was preserved, at least locally, up to the late Cretaceous, and was not entirely destroyed during the breakup of Gondwana, as inferred by some recent geophysical models.
Geological Society of London, Special Publication: Monogenetic volcanism, no. 446, pp. 205-224.
Canada, Ontario, Attawapiskat
deposit - Tango
Abstract: Extensive drilling of the Tango Extension kimberlite pipe resulted in the construction of an emplacement model that revealed the complex architecture of two amalgamated pipes: an older pipe, the Tango Extension Deep, which is cut along its northern margin by the smaller Tango Extension pipe. The resulting volcano forms a complex pipe-in-pipe structure called the Tango Extension Super Structure. The emplacement of the Tango Extension Super Structure sequence indicates prolonged hiatuses, which, similar to other volcanoes classified as monogenetic, puts the classical monogenetic and polygenetic definitions of maar-diatreme volcanoes to the test. Although the Tango Extension and Tango Extension Deep volcanoes could be characterized individually as monogenetic volcanoes, the Tango Extension Super Structure shows evidence of the occurrence of the significant hiatuses typical of polygenetic volcanoes. We suggest that hiatuses that are long enough to consolidate earlier tephra unambiguously differentiate polygenetic from monogenetic maar-diatreme volcanoes.
Abstract: The petrogenesis of kimberlites is commonly obscured by interaction with hydrothermal fluids, including deuteric (late-magmatic) and/or groundwater components. To provide new constraints on the modification of kimberlite rocks during fluid interaction and the fractionation of kimberlite magmas during crystallisation, we have undertaken a detailed petrographic and geochemical study of a hypabyssal sample (BK) from the Bultfontein kimberlite (Kimberley, South Africa). Sample BK consists of abundant macrocrysts (> 1 mm) and (micro-) phenocrysts of olivine and lesser phlogopite, smaller grains of apatite, serpentinised monticellite, spinel, perovskite, phlogopite and ilmenite in a matrix of calcite, serpentine and dolomite. As in kimberlites worldwide, BK olivine grains consist of cores with variable Mg/Fe ratios, overgrown by rims that host inclusions of groundmass phases (spinel, perovskite, phlogopite) and have constant Mg/Fe, but variable Ni, Mn and Ca concentrations. Primary multiphase inclusions in the outer rims of olivine and in Fe-Ti-rich (‘MUM’) spinel are dominated by dolomite, calcite and alkali carbonates with lesser silicate and oxide minerals. Secondary inclusions in olivine host an assemblage of Na-K carbonates and chlorides. The primary inclusions are interpreted as crystallised alkali-Si-bearing Ca-Mg-rich carbonate melts, whereas secondary inclusions host Na-K-rich C-O-H-Cl fluids. In situ Sr-isotope analyses of groundmass calcite and perovskite reveal similar 87Sr/86Sr ratios to perovskite in the Bultfontein and the other Kimberley kimberlites, i.e. magmatic values. The ?18O composition of the BK bulk carbonate fraction is above the mantle range, whereas the ?13C values are similar to those of mantle-derived magmas. The occurrence of different generations of serpentine and occasional groundmass calcite with high 87Sr/86Sr, and elevated bulk carbonate ?18O values indicate that the kimberlite was overprinted by hydrothermal fluids, which probably included a significant groundwater component. Before this alteration the groundmass included calcite, monticellite, apatite and minor dolomite, phlogopite, spinel, perovskite and ilmenite. Inclusions of groundmass minerals in olivine rims and phlogopite phenocrysts show that olivine and phlogopite also belong to the magmatic assemblage. We therefore suggest that the crystallised kimberlite was produced by an alkali-bearing, phosphorus-rich, silica-dolomitic melt. The alkali-Si-bearing Ca-Mg-rich carbonate compositions of primary melt inclusions in the outer rims of olivine and in spinel grains with evolved compositions (MUM spinel) support formation of these melts after fractionation of abundant olivine, and probably other phases (e.g., ilmenite and chromite). Finally, the similarity between secondary inclusions in kimberlite olivine of this and other worldwide kimberlites and secondary inclusions in minerals of carbonatitic, mafic and felsic magmatic rocks, suggests trapping of residual Na-K-rich C-O-H-Cl fluids after groundmass crystallisation. These residual fluids may have persisted in pore spaces within the largely crystalline BK groundmass and subsequently mixed with larger volumes of external fluids, which triggered serpentine formation and localised carbonate recrystallisation.
Abstract: Alkaline carbonates hexagonal zemkorite (Na,K)2Ca(CO3)2 and orthorhombic shortite Na2Ca2(CO3)3 were found among groundmass minerals in kimberlites from some localities worldwide, including the unserpentinised units of the Udachnaya-East kimberlite. However, the source of alkalis and the origin of the unusual minerals in these kimberlites remain highly debatable. It is generally considered that they have hydrothermal or metasomatic origin while sodium may come from a crustal source. Orthorhombic nyerereite (Na,K)2Ca(CO3)2 and shortite were identified as daughter phases in secondary melt inclusions (MI) in olivine from the deepest mantle xenoliths (i.e., sheared peridotites) and in olivine xenocrysts derived from disintegrated mantle rocks from the Udachnaya-East pipe by Raman spectroscopy and SEM-EDS. The melt, hosted as the inclusions in olivine, was entrapped at a mantle depth. On the basis of similar mineralogy of MI to groundmass of the unserpentinised kimberlites, we suggest relation of MI to the Udachnaya kimberlite melts. The MI solidus temperature is as high as 500 °?. Generally, MI nyerereite is considered as a magmatic mineral but experiments show it to be stable at relatively low temperatures (LT) T ? 360 °?. Thus, strictly speaking, it is a subsolidus mineral formed from high-temperature (HT) (T < 800 °?) hexagonal (Na,K)2Ca(CO3)2 carbonate. Shortite is also a subsolidus mineral, which may form by several subsolidus reactions in multicomponent systems, such as kimberlites, while breakdown of the HT hexagonal phase (Na,K)2Ca(CO3,SO4)2 into Na2Ca2(CO3)3 (shortite) and K3Na(SO4)2 (aphthitalite) is the basic mechanism. The solidus temperature for the Udachnaya-East kimberlite is about 300 °? indicating that LT orthorhombic nyerereite may crystallise directly from the melt as well. Thus, (Na,K)2Ca(CO3)2 and Na2Ca2(CO3)3 carbonates in the groundmass of the unserpentinised Udachnaya-East kimberlites are of magmatic/subsolidus origin. This scenario for the origin of Na-K-Ca and Na-Ca carbonates in the Udachnaya-East kimberlites may have implications for other kimberlites elsewhere.
Abstract: The results of integrated studies of inclusion-containing diamonds from kimberlites of the Snap Lake dike complex (Canada) are presented. Features of the morphology, defect–impurity composition, and internal structure of the diamonds were determined by optic and scanning microscopy. The chemical composition of crystalline inclusions (olivine, garnet, and pyroxene) in diamonds was studied using a microanalyzer with an electronic probe. The inclusions of ultramafic paragenesis in the diamond (87%) are predominant. Carbonates, sulfide and hydrated silicate phases were found only in multiphase microinclusions. The large phlogopite inclusion studied was similar in composition to earlier studied nanosize inclusions of high-silica mica in diamonds from Snap Lake kimberlites. Revealed features of studied diamonds and presence of high-silica mica suggest that diamonds from Snap Lake have formed as the result of interaction between enriched in volatile and titanium high-potassium carbonate–silicate melts and peridotitic substrate at the base of thick lithospheric mantle.
Abstract: Kimberlites of the Udachnaya-East pipe (Siberia) include a uniquely dry and serpentine-free rock type with anomalously high contents of chlorine (Cl ? 6.1 wt%), alkalies (Na2O + K2O ? 10 wt%) and sulfur (S ? 0.50 wt%), referred to as a “salty” kimberlite. The straightforward interpretation is that the Na-, K-, Cl- and S-rich components originate directly from a carbonate-chloride kimberlitic magma that is anhydrous and alkali-rich. However, because brines and evaporites are present on the Siberian craton, previous studies proposed that the kimberlitic magma was contaminated by the assimilation of salt-rich crustal rocks. To clarify the origin of high Cl, alkalies and S in this unusual kimberlite, here we determine its sulfur speciation and isotopic composition and compare it to that of non-salty kimberlites and kimberlitic breccia from the same pipe, as well as potential contamination sources (hydrothermal sulfides and sulfates, country-rock sediment and brine collected in the area). The average ?34S of sulfides is ? 1.4 ± 2.2‰ in the salty kimberlite, 2.1 ± 2.7‰ in the non-salty kimberlites and 14.2 ± 5.8‰ in the breccia. The average ?34S of sulfates in the salty kimberlites is 11.1 ± 1.8‰ and 27.3 ± 1.6‰ in the breccia. In contrast, the ?34S of potential contaminants range from 20 to 42‰ for hydrothermal sulfides, from 16 to 34‰ for hydrothermal sulfates, 34‰ for a country-rock sediment (Chukuck suite) and the regional brine aquifer. Our isotope analyses show that (1) in the salty kimberlites, neither sulfates nor sulfides can be simply explained by brine infiltration, hydrothermal alteration or the assimilation of known salt-rich country rocks and instead, we propose that they are late magmatic phases; (2) in the non-salty kimberlite and breccia, brine infiltration lead to sulfate reduction and the formation of secondary sulfides – this explains the removal of salts, alkali-carbonates and sulfates, as well as the minor olivine serpentinization; (3) hydrothermal sulfur was added to the kimberlitic breccia, but not to the massive kimberlites. In situ measurements of sulfides confirm this scenario, clearly showing the addition of two sulfide populations in the breccia (pyrite-pyrrhotites with average ?34S of 7.9 ± 3.4‰ and chalcopyrites with average ?34S of 38.0 ± 0.4‰) whereas the salty and non-salty kimberlites preserve a unique population of djerfisherites (Cl- and K-rich sulfides) with ?34S values within the mantle range. This study provides the first direct evidence of alkaline igneous rocks in which magmatic sulfate is more abundant than sulfide. Although sulfates have been rarely reported in mantle materials, sulfate-rich melts may be more common in the mantle than previously thought and could balance the sulfur isotope budget of Earth's mantle.
Academia.edu, Supplementary material app. 1 and 2, both 10p.
Asia, Kalimantan
deposit - Kalimantan
Abstract: Diamonds in alluvial deposits in Southeast Asia are not accompanied by indicator minerals suggesting primary kimberlite or lamproite sources. The Meratus Mountains in Southeast Borneo (Province Kalimantan Selatan, Indonesia) provide the largest known deposit of these so-called “headless” diamond deposits. Proposals for the origin of Kalimantan diamonds include the adjacent Meratus ophiolite complex, ultra-high pressure (UHP) metamorphic terranes, obducted subcontinental lithospheric mantle and undiscovered kimberlite-type sources. Here we report results from detailed sediment provenance analysis of diamond-bearing Quaternary river channel material and from representative outcrops of the oldest known formations within the Alino Group, including the diamond-bearing Campanian–Maastrichtian Manunggul Formation. Optical examination of surfaces of diamonds collected from artisanal miners in the Meratus area (247 stones) and in West Borneo (Sanggau Area, Province Kalimantan Barat; 85 stones) points toward a classical kimberlite-type source for the majority of these diamonds. Some of the diamonds host mineral inclusions suitable for deep single-crystal X-ray diffraction investigation. We determined the depth of formation of two olivines, one coesite and one peridotitic garnet inclusion. Pressure of formation estimates for the peridotitic garnet at independently derived temperatures of 930–1250 °C are between 4.8 and 6.0 GPa. Sediment provenance analysis includes petrography coupled to analyses of detrital garnet and glaucophane. The compositions of these key minerals do not indicate kimberlite-derived material. By analyzing almost 1400 zircons for trace element concentrations with laser ablation ICP-MS (LA-ICP-MS) we tested the mineral's potential as an alternative kimberlite indicator. The screening ultimately resulted in a small subset of ten zircons with a kimberlitic affinity. Subsequent U–Pb dating resulting in Cretaceous ages plus a detailed chemical reflection make a kimberlitic origin unfavorable with respect to the regional geological history. Rather, trace elemental analyses (U, Th and Eu) suggest an eclogitic source for these zircons. The age distribution of detrital zircons allows in general a better understanding of collisional events that formed the Meratus orogen and identifies various North Australian Orogens as potential Pre-Mesozoic sediment sources. Our data support a model whereby the majority of Kalimantan diamonds were emplaced within the North Australian Craton by volcanic processes. Partly re-deposited into paleo-collectors or residing in their primary host, these diamond-deposits spread passively throughout Southeast Asia by terrane migration during the Gondwana breakup. Terrane amalgamation events largely metamorphosed these diamond-bearing lithologies while destroying the indicative mineral content. Orogenic uplift finally liberated their diamond-content into new, autochthonous placer deposits.
Geochimica et Cosmochimica Acta, available in press 23p.
Africa, Botswana
deposit - Orapa
Abstract: Base metal sulphide (BMS) inclusions in diamonds provide a unique insight into the chalcophile and highly siderophile element composition of the mantle. Entombed within their diamond hosts, these provide a more robust (closed system) sample, from which to determine the trace element, Re-Os and S-isotopic compositions of the mantle than mantle xenoliths or orogenic peridotites, as they are shielded from alteration during ascent to the Earth’s crust and subsequent surface weathering. However, at temperatures below 1100 °C some BMS inclusions undergo subsolidus re-equilibration from an original monosulphide solid solution (Mss) and this causes fractionation of the major and trace elements within the inclusions. Thus to study the subjects noted above, current techniques require the entire BMS inclusion to be extracted for analyses. Unfortunately, ‘flaking’ of inclusions during break-out is a frequent occurrence and hence the risk of accidentally under-sampling a portion of the BMS inclusion is inherent in current practices. This loss may have significant implications for Re-Os isotope analyses where incomplete sampling of a Re-rich phase, such as chalcopyrite that typically occurs at the outer margins of BMS inclusions, may induce significant bias in the Re-Os and 187Os/188Os measurements and resulting model and isochron ages. We have developed a method for the homogenisation of BMS inclusions in diamond prior to their break-out from the host stone. Diamonds are heated to 1100 °C and then quenched to chemically homogenise any sulphide inclusions for both major and trace elements. Using X-ray Computed Microtomography (µCT) we determine the shape and spatial setting of multiple inclusions within a host stone and crucially show that the volume of a BMS inclusion is the same both before and after homogenisation. We show that the homogenisation process significantly reduces the inherent variability of in situ analysis when compared with unhomogenised BMS, thereby widening the scope for multiple methods for quantitative analysis, even on ‘flakes’ of single BMS inclusions. Finally we show that the trace elements present in peridotite (P-type) and eclogitic (E-type) BMS are distinct, with P-type diamonds having systematically higher total platinum-group element (particularly Os, Ir, Ru) and Te and As concentrations. These distinctions suggest that the PGE and semi-metal budgets of mantle-derived partial melts will be significantly dependent upon the type(s) and proportions of sulphides present in the mantle source.
Abstract: The paper presents data on the composition of olivine macrocrysts from two Devonian kimberlite pipes in the Arkhangelsk diamond province: the Grib pipe (whose kimberlite belongs to type I) and Pionerskaya pipe (whose kimberlite is of type II, i.e., orangeite). The dominant olivine macrocrysts in kimberlites from the two pipes significantly differ in geochemical and isotopic parameters. Olivine macrocrysts in kimberlite from the Grib pipe are dominated by magnesian (Mg# = 0.92–0.93), Ti-poor (Ti < 70 ppm) olivine possessing low Ti/Na (0.05–0.23), Zr/Nb (0.28–0.80), and Zn/Cu (3–20) ratios and low Li concentrations (1.2–2.0 ppm), and the oxygen isotopic composition of this olivine ?18O = 5.64‰ is higher than that of olivine in mantle peridotites (?18O = 5.18 ± 0.28‰). Olivine macrocrysts in kimberlite from the Pionerskaya pipe are dominated by varieties with broadly varying Mg# = 0.90–0.93, high Ti concentrations (100–300 ppm), high ratios Ti/Na (0.90–2.39), Zr/Nb (0.31–1.96), and Zn/Cu (12–56), elevated Li concentrations (1.9–3.4 ppm), and oxygen isotopic composition ?18O = 5.34‰ corresponding to that of olivine in mantle peridotites. The geochemical and isotopic traits of low-Ti olivine macrocrysts from the Grib pipe are interpreted as evidence that the olivine interacted with carbonate-rich melts/fluids. This conclusion is consistent with the geochemical parameters of model melt in equilibrium with the low-Ti olivine that are similar to those of deep carbonatite melts. Our calculations indicate that the variations in the ?18O of the olivine relative the “mantle range” (toward both higher and lower values) can be fairly significant: from 4 to 7‰ depending on the composition of the carbonate fluid. These variations were formed at interaction with carbonate fluid, whose ?18O values do not extend outside the range typical of mantle carbonates. The geochemical parameters of high-Ti olivine macrocrysts from the Grib pipe suggest that their origin was controlled by the silicate (water–silicate) component. This olivine is characterized by a zoned Ti distribution, with the configuration of this distribution between the cores of the crystals and their outer zones showing that the zoning of the cores and outer zones is independent and was produced during two episodes of reaction interaction between the olivine and melt/fluid. The younger episode (when the outer zone was formed) likely involved interaction with kimberlite melt. The transformation of the composition of the cores during the older episode may have been of metasomatic nature, as follows from the fact that the composition varies from grain to grain. The metasomatic episode most likely occurred shortly before the kimberlite melt was emplaced and was related to the partial melting of pyroxenite source material.
Abstract: The paper presents data on the composition of olivine macrocrysts from two Devonian kimberlite pipes in the Arkhangelsk diamond province: the Grib pipe (whose kimberlite belongs to type I) and Pionerskaya pipe (whose kimberlite is of type II, i.e., orangeite). The dominant olivine macrocrysts in kimberlites from the two pipes significantly differ in geochemical and isotopic parameters. Olivine macrocrysts in kimberlite from the Grib pipe are dominated by magnesian (Mg# = 0.92–0.93), Ti-poor (Ti < 70 ppm) olivine possessing low Ti/Na (0.05–0.23), Zr/Nb (0.28–0.80), and Zn/Cu (3–20) ratios and low Li concentrations (1.2–2.0 ppm), and the oxygen isotopic composition of this olivine ?18O = 5.64‰ is higher than that of olivine in mantle peridotites (?18O = 5.18 ± 0.28‰). Olivine macrocrysts in kimberlite from the Pionerskaya pipe are dominated by varieties with broadly varying Mg# = 0.90–0.93, high Ti concentrations (100–300 ppm), high ratios Ti/Na (0.90–2.39), Zr/Nb (0.31–1.96), and Zn/Cu (12–56), elevated Li concentrations (1.9–3.4 ppm), and oxygen isotopic composition ?18O = 5.34‰ corresponding to that of olivine in mantle peridotites. The geochemical and isotopic traits of low-Ti olivine macrocrysts from the Grib pipe are interpreted as evidence that the olivine interacted with carbonate-rich melts/fluids. This conclusion is consistent with the geochemical parameters of model melt in equilibrium with the low-Ti olivine that are similar to those of deep carbonatite melts. Our calculations indicate that the variations in the ?18O of the olivine relative the “mantle range” (toward both higher and lower values) can be fairly significant: from 4 to 7‰ depending on the composition of the carbonate fluid. These variations were formed at interaction with carbonate fluid, whose ?18O values do not extend outside the range typical of mantle carbonates. The geochemical parameters of high-Ti olivine macrocrysts from the Grib pipe suggest that their origin was controlled by the silicate (water–silicate) component. This olivine is characterized by a zoned Ti distribution, with the configuration of this distribution between the cores of the crystals and their outer zones showing that the zoning of the cores and outer zones is independent and was produced during two episodes of reaction interaction between the olivine and melt/fluid. The younger episode (when the outer zone was formed) likely involved interaction with kimberlite melt. The transformation of the composition of the cores during the older episode may have been of metasomatic nature, as follows from the fact that the composition varies from grain to grain. The metasomatic episode most likely occurred shortly before the kimberlite melt was emplaced and was related to the partial melting of pyroxenite source material.
Abstract: Oldoinyo Lengai is situated within the Gregory Rift Valley (northern Tanzania) and is the only active volcano erupting natrocarbonatite lava. This study investigates the texture and mineralogy of the June 1993 lava at Oldoinyo Lengai, and presents petrographic evidence of liquid immiscibility between silicate, carbonate, chloride, and fluoride melt phases. The 1993 lava is a porphyritic natrocarbonatite consisting of abundant phenocrysts of alkali carbonates, nyerereite and gregoryite, set in a quenched groundmass, composed of sodium carbonate, khanneshite, Na-sylvite and K-halite, and a calcium fluoride phase. Dispersed in the lava are silicate spheroids (< 2 mm) with a cryptocrystalline silicate mineral assemblage wrapped around a core mineral. We have identified several textural features preserved in the silicate spheroids, melt inclusions, and carbonatite groundmass that exhibit evidence of silicate-carbonate, carbonate-carbonate and carbonate-halide immiscibility. Rapid quenching of the lava facilitated the preservation of the end products of these liquid immiscibility processes within the groundmass. Textural evidence (at both macro- and micro-scales) indicates that the silicate, carbonate, chloride and fluoride phases of the lava unmixed at different stages of evolution in the magmatic system.
Abstract: A mineralogical study of the hypabyssal facies, late Cretaceous macrocrystic pulse of TK1 intrusion and the Mesoproterozoic aphanitic pulse of TK4 intrusion in the Wajrakarur Kimberlite Field of southern India shows that the rocks contain macrocrysts of forsteritic olivine, phenocrysts and microphenocrysts of Al–Na-poor diopside and phlogopite set in a groundmass mainly of Al–Na-poor diopside and phlogopite. Other groundmass minerals are spinel, perovskite and fluorapatite in TK1, and spinel, titanite, chlorite, calcite and gittinsite in TK4. K-richterite and perovskite occur only as inclusions in phlogopite and titanite, respectively in TK4. Late-stage deuteric phases include pyrite and barite in TK1, and strontianite, chalcopyrite, galena and pentlandite in TK4. Diopside microphenocrysts in TK4 exhibit oscillatory zoning with characteristics of diffusion controlled magmatic growth. TK1 spinels show magmatic trend 2 that evolves from magnesiochromite and culminates in titaniferous magnetite, whereas TK4 spinels are less evolved with magnesiochromite composition only. TK1 phlogopites show a simple compositional trend that is typical of lamproite micas, while four distinct growth zones are observed in TK4 phlogopites with the following compositional characteristics: zone I: high Cr2O3 and TiO2 and low BaO; zone II: low Cr2O3; zone III: low TiO2 and high BaO; zone IV: low BaO. Forsterite contents and trace element concentrations reveal two xenocrystic core populations and one magmatic rim population for TK1 olivines. Mineralogically, both TK1 and TK4 are classified as diopside–phlogopite lamproites rather than archetypal kimberlites. The two lamproites are considered to have formed from the same parent magma but crystallised under distinct oxygen fugacity conditions. With elevated content of Fe3 + in phlogopite, spinel and perovskite, TK1 appears to have crystallised in a relatively high oxygen fugacity environment. Multiple growth generations of phlogopite, spinel and fluorapatite in TK4 indicate a complex evolutionary history of the magma. Close spatial and temporal associations of Mesoproterozoic kimberlites and lamproites in southern India can possibly be explained by a unifying model which accounts for the generation of diverse magmas from a range of geochemical resevoirs in a continental rift setting.
Abstract: Notable within-crystal variability of mineralogical and geochemical properties of single natural diamonds are commonly attributed to changing chemistry of parental fluids, sources of carbon and redox conditions of diamond precipitation. A distinct type of compositional heterogeneity (mixed-habit structure) is well-known to occur in diamonds as well as in many other minerals due to purely “structural” reasons that are unequal crystal chemistry of crystallographically different faces and selective absorption and fractionation of impurities between adjacent growth pyramids. Based on the combined cathodoluminescence, Fourier-transformed infrared spectroscopy and photoluminescence spectroscopy, study of nine diamond crystals with different growth histories and external morphology, but all showing mixed-habit patterns at different growth stages, we show that mixed-diamonds may grow in closed system conditions or with a slowly decreasing growth rate from a media with a much lower impurity content than previously thought. Intracrystal nitrogen distribution seems to be a function of growth rate even in the cases of unusual impurity partitioning between growth sectors. Generally poor with IR-active hydrogen at moderate nitrogen aggregation parameters, studied diamonds likely resemble the low hydrogen content from the growth medium that, for cubic diamonds, was typically suggested hydrogen-rich and a crucial factor for growth of cubic and mixed-habit diamonds. We also show that mixed-habit diamond growth may occur not only in peridotitic suite but also in an extended field of geochemical affinities from high-Ni to low-Ni or maybe even Ni-free environments, such as pyroxenitic or eclogitic.
Abstract: Notable within-crystal variability of mineralogical and geochemical properties of single natural diamonds are commonly attributed to changing chemistry of parental fluids, sources of carbon and redox conditions of diamond precipitation. A distinct type of compositional heterogeneity (mixed-habit structure) is well-known to occur in diamonds as well as in many other minerals due to purely “structural” reasons that are unequal crystal chemistry of crystallographically different faces and selective absorption and fractionation of impurities between adjacent growth pyramids. Based on the combined cathodoluminescence, Fourier-transformed infrared spectroscopy and photoluminescence spectroscopy, study of nine diamond crystals with different growth histories and external morphology, but all showing mixed-habit patterns at different growth stages, we show that mixed-diamonds may grow in closed system conditions or with a slowly decreasing growth rate from a media with a much lower impurity content than previously thought. Intracrystal nitrogen distribution seems to be a function of growth rate even in the cases of unusual impurity partitioning between growth sectors. Generally poor with IR-active hydrogen at moderate nitrogen aggregation parameters, studied diamonds likely resemble the low hydrogen content from the growth medium that, for cubic diamonds, was typically suggested hydrogen-rich and a crucial factor for growth of cubic and mixed-habit diamonds. We also show that mixed-habit diamond growth may occur not only in peridotitic suite but also in an extended field of geochemical affinities from high-Ni to low-Ni or maybe even Ni-free environments, such as pyroxenitic or eclogitic.
Abstract: Notable within-crystal variability of mineralogical and geochemical properties of single natural diamonds are commonly attributed to changing chemistry of parental fluids, sources of carbon and redox conditions of diamond precipitation. A distinct type of compositional heterogeneity (mixed-habit structure) is well-known to occur in diamonds as well as in many other minerals due to purely “structural” reasons that are unequal crystal chemistry of crystallographically different faces and selective absorption and fractionation of impurities between adjacent growth pyramids. Based on the combined cathodoluminescence, Fourier-transformed infrared spectroscopy and photoluminescence spectroscopy, study of nine diamond crystals with different growth histories and external morphology, but all showing mixed-habit patterns at different growth stages, we show that mixed-diamonds may grow in closed system conditions or with a slowly decreasing growth rate from a media with a much lower impurity content than previously thought. Intracrystal nitrogen distribution seems to be a function of growth rate even in the cases of unusual impurity partitioning between growth sectors. Generally poor with IR-active hydrogen at moderate nitrogen aggregation parameters, studied diamonds likely resemble the low hydrogen content from the growth medium that, for cubic diamonds, was typically suggested hydrogen-rich and a crucial factor for growth of cubic and mixed-habit diamonds. We also show that mixed-habit diamond growth may occur not only in peridotitic suite but also in an extended field of geochemical affinities from high-Ni to low-Ni or maybe even Ni-free environments, such as pyroxenitic or eclogitic.
Abstract: Notable within-crystal variability of mineralogical and geochemical properties of single natural diamonds are commonly attributed to changing chemistry of parental fluids, sources of carbon and redox conditions of diamond precipitation. A distinct type of compositional heterogeneity (mixed-habit structure) is well-known to occur in diamonds as well as in many other minerals due to purely “structural” reasons that are unequal crystal chemistry of crystallographically different faces and selective absorption and fractionation of impurities between adjacent growth pyramids. Based on the combined cathodoluminescence, Fourier-transformed infrared spectroscopy and photoluminescence spectroscopy, study of nine diamond crystals with different growth histories and external morphology, but all showing mixed-habit patterns at different growth stages, we show that mixed-diamonds may grow in closed system conditions or with a slowly decreasing growth rate from a media with a much lower impurity content than previously thought. Intracrystal nitrogen distribution seems to be a function of growth rate even in the cases of unusual impurity partitioning between growth sectors. Generally poor with IR-active hydrogen at moderate nitrogen aggregation parameters, studied diamonds likely resemble the low hydrogen content from the growth medium that, for cubic diamonds, was typically suggested hydrogen-rich and a crucial factor for growth of cubic and mixed-habit diamonds. We also show that mixed-habit diamond growth may occur not only in peridotitic suite but also in an extended field of geochemical affinities from high-Ni to low-Ni or maybe even Ni-free environments, such as pyroxenitic or eclogitic.
Abstract: Mantle-derived eclogite and pyroxenite xenoliths from the Jurassic Voyageur kimberlite on the northern Slave craton in Arctic Canada were studied for garnet and clinopyroxene major and trace element compositions, clinopyroxene Pb and garnet O isotopic compositions, and garnet Fe3 +/?Fe contents. The Voyageur xenoliths record a wide range of pressures, but are cooler compared to mantle xenoliths derived from the nearby, coeval Jericho kimberlite. The CaO, TiO2 and Zr contents of Voyageur eclogites increase with depth, which is also observed in northern Slave peridotite xenoliths, demonstrating ‘bottom-up’ metasomatic processes within cratonic mantle lithosphere. The Voyageur eclogites have positive Eu anomalies, flat HREEN patterns, and major element compositions that are consistent with ultimate origins from basaltic and gabbroic protoliths within oceanic lithosphere. Clinopyroxene Pb isotope ratios intercept the Stacey-Kramers two-stage terrestrial Pb evolution curve at ca. 2.1 Ga, and form an array towards the host kimberlite, indicating isotopic mixing. The 2.1 Ga eclogite formation age broadly overlaps with known Paleoproterozoic subduction and collision events that occurred along the western margin of the Slave craton. Unlike the eclogites, the Voyageur pyroxenites contain garnet with distinctive fractionated HREEN, sinusoidal REE patterns of calculated bulk rocks, and clinopyroxene with 206Pb/204Pb ratios that intercept the Stacey-Kramers curve at 1.8 Ga. This suggests a distinct origin as Paleoproterozoic high-pressure mantle cumulates. However, the pyroxenite Pb isotope ratios fall within the eclogite array and could also be explained by protoliths formation at ca. 2.1 Ga followed by minor isotopic mixing during mantle metasomatism. Thus, an alternative scenario involves pyroxenite formation within the mantle section of Paleoproterozoic oceanic lithosphere followed by variable metasomatism after incorporation into cratonic mantle lithosphere. This model allows for a linked petrogenesis of the Voyageur eclogites (crust) and pyroxenites (mantle) as part of the same subducting oceanic slab. Oxygen fugacity determinations for one pyroxenite and ten eclogite xenoliths show a range of 3 log units, from ? 4.6 to ? 1.6 ?FMQ, similar to the range observed for nearby Jericho and Muskox eclogites (?FMQ ? 4.2 to ? 1.5). Importantly, the northern Slave eclogite and pyroxenite mantle components are highly heterogeneous in terms of redox state provided that they range from reduced to oxidized relative to Slave peridotite xenoliths. Moreover, the Voyageur eclogites do not exhibit any trend between oxidation state and equilibration depth, which contrasts with the downward decrease in fO2 shown by Slave and worldwide cratonic peridotite xenoliths. Our investigation of mantle eclogite and pyroxenite fO2 reinforces the important influence of recycled mafic components in upper mantle processes, because their high and variable redox buffering capacity strongly controls volatile speciation and melting relations under upper mantle conditions.
Abstract: Carbon isotope compositions and the distribution of nitrogen and hydrogen in diamonds from 18 eclogites from Nurbinskaya kimberlites were studied in situ in polished plates. Cathodoluminescence images show that most of the diamonds have complex growth structures with distinctive core, intermediate and rim zones. In some diamonds the cores display dissolution features, and intermediate growth zones are separated from the cores by narrow rounded oscillatory zones. At least three crystals show interrupted multistage diamond growth; variations in ?13C of 2–3‰ occur across the contacts between distinct zones. Generally, ?13C within the diamond cores varies only by 1–2‰, in rare cases up to 3.3‰. ?13C values are usually lower in the intermediate zones and drop further towards the rims by up to 3‰. High-resolution SIMS profiles show that variations in ?13C across the diamond growth zones are sharp with no evidence of diffusive relaxation. Diamonds with predominantly tangential octahedral growth have a wide range in ?13C from ? 15.2‰ up to 9.0‰ (± 0.4‰), and their nitrogen (N) contents vary between 30 and 1500 at. ppm. Six diamonds show little internal variation along the isotopic profiles with changes in ?13C of only 0.3–0.9‰ around mean values ranging from ? 6‰ to ? 3‰. Five crystals are isotopically heavy, with relatively homogeneous ?13C up to 9‰. FTIR data show markedly different N concentrations and nitrogen aggregation states between major growth zones. This implies that the diamonds in eclogitic xenoliths from Nyurbinskaya pipe grew in multiple and interrupted growth events, probably from fluids enriched in K and H. The wide variations of ?13C in the studied eclogitic diamonds and identification of their anomalously positive ?13C values, combined with the wide range of high ?18O in garnets from the diamondiferous xenoliths of the Nyurbinskaya pipe, which are mostly outside of the mantle range, suggest a crustal contribution to the parental mantle-related fluids forming diamonds in these xenoliths and indicate the complex metasomatic evolution of the lithospheric mantle beneath the Nakynsky kimberlite field.
Earth and Planetary Science Letters, Vol. 473, pp. 44-51.
Africa, Zimbabwe
deposit - Marange
Abstract: Because of the inability of depleted cratonic peridotites to effectively buffer oxygen fugacities when infiltrated by CHO or carbonatitic fluids, it has been proposed recently (Luth and Stachel, 2014) that diamond formation in peridotites typically does not occur by rock-buffered redox reactions as previously thought but by an oxygen-conserving reaction in which minor coexisting CH4 and CO2 components in a water-rich fluid react to form diamond (CO2 + CH4 = 2C + 2H2O). In such fluid-buffered systems, carbon isotope fractionation during diamond precipitation occurs in the presence of two dominant fluid carbon species. Carbon isotope modelling of diamond precipitation from mixed CH4CH4- and CO2-bearing fluids reveals unexpected fundamental differences relative to diamond crystallization from a single carbon fluid species: (1) irrespective of which carbon fluid species (CH4 or CO2) is dominant in the initial fluid, diamond formation is invariably associated with progressive minor (<1‰) enrichment of diamond in 13C as crystallization proceeds. This is in contrast to diamond precipitation by rock-buffered redox processes from a fluid containing only a single carbon species, which can result in either progressive 13C enrichment (CO2 or carbonate fluids) or View the MathML sourceC13 depletion (CH4 fluids) in the diamond. (2) Fluid speciation is the key factor controlling diamond ?13C?13C values; as XCO2 (XCO2 = CO2/[CO2 + CH4]) in the initial fluid increases from 0.1 to 0.9 (corresponding to an increase in fO2fO2 of 0.8 log units), the carbon isotope composition of the first-precipitated diamond decreases by 3.7‰. The tight mode in ?13C of ?5 ±1‰?5 ±1‰ for diamonds worldwide places strict constraints on the dominant range of XCO2 in water-rich fluids responsible for diamond formation. Specifically, precipitation of diamonds with ?13C values in the range ?4 to ?6‰ from mantle-derived fluids with an average ?13C value of ?5‰ (derived from evidence not related to diamonds) requires that diamond-forming fluids were relatively reduced and had methane as the dominant carbon species (XCO2 = 0.1–0.5). Application of our model to a recently published set of in-situ carbon isotope analyses for peridotitic diamonds from Marange, Zimbabwe (Smit et al., 2016), which contain CH4 fluid inclusions, allows us to perfectly match the observed co-variations in ?13C?13C, ?15N?15N and N content and at the same time explain the previously counter-intuitive observation of progressive View the MathML sourceC13 enrichment in diamonds that appear to have grown from a fluid with methane as the dominant carbon species. Similarly, the almost complete absence in the published record of progressive View the MathML sourceC13 depletion trends within diamonds likely reflects ubiquitous precipitation from CH4- and CO2-bearing water-rich fluids, rather than diamond formation exclusively by carbonate-bearing and CH4-free oxidized fluids or melts.
Abstract: Neoproterozoic kimberlite, ultramafic lamprophyre, and carbonatite magmatic activity was widespread across the Canadian-Greenland Shield. Models to explain the preponderance of this deeply-derived CO2-rich magmatism between 680–540 Ma range from impingement of multiple mantle plumes to rifting activity linked to the breakout of the Laurentian plate from the Rodinia supercontinent configuration. We add to the debate about the origin of kimberlite magmas and evaluate possible mantle sources of the 655 Ma ‘diamond-rich’ Renard (new SIMS U/Pb perovskite ages) and 629 Ma ‘barren’ Wemindji kimberlites on the eastern Superior craton in Quebec, Canada. Our Sr-Nd-Hf and carbon isotope data (87Sr/86Sri = 0.70241–0.70442; ?Ndi = + 0.2 to + 4.8; ?Hfi = + 0.3 to + 6.5; ?13C = ? 5.6 to ? 3.9‰) suggest a common and moderately depleted convecting upper mantle source region for both the Renard and Wemindji kimberlites, which occur 400 km apart in the interior of the Superior craton. In contrast, the low Os isotope ratios (187Os/188Osi = 0.11078–0.12620; ?Osi = ? 13.7 to ? 1.6) and unfractionated chondritic relative HSE abundances (Os, Ir, Ru, Pt, Pd, Re) indicate significant involvement of ancient refractory cratonic mantle material in kimberlite magma formation. Our model calculations suggest that for both the diamond-rich Renard and the barren Wemindji kimberlite magmas up to 30% of the Os was derived from refractory cratonic peridotites. This material might have been assimilated by originally more CO2-rich carbonated silicate melts derived from the asthenosphere. We also show that the geochemical and Sr-Nd-Hf-Os isotopic compositions of the Renard and Wemindji kimberlites do not require significant input from melts derived from olivine-poor cratonic mantle lithologies such as MARID-type veins and pyroxenites/eclogites. This contrasts with the petrogenesis of deeply-derived volatile-rich potassic magmas found along the peripheries of cratons (e.g., ultramafic lamprophyres, kamafugites, and olivine lamproites), a setting where abundant non-peridotitic components have been added to the lithospheric mantle over the course of continent evolution. Provided that CO2-rich melts, such as proto-kimberlites, occur near the solidus of volatile-fluxed peridotites, no excess mantle heat is required in their formation. This important but often overlooked constraint, together with the observation that there exist no spatial or temporal relationships between the Superior craton kimberlites and Large Igneous Provinces during the Late Neoproterozoic, suggests that kimberlite magmatic activity was tectonically controlled. In our preferred model, ubiquitous CO2-rich proto-kimberlite melts form during volatile-controlled redox melting processes at ambient mantle temperatures in a thermal boundary layer directly beneath thick cratonic lithosphere. The success rate of ‘evolving’ hybrid kimberlite magmas reaching Earth’s surface increases when tensile stresses propagate into the > 200 km thick keels of continental lithosphere. These conditions are frequently met during fast and changing plate motions associated with the assembly and breakup of supercontinents.
Abstract: Neoproterozoic kimberlite, ultramafic lamprophyre, and carbonatite magmatic activity was widespread across the Canadian-Greenland Shield. Models to explain the preponderance of this deeply-derived CO2-rich magmatism between 680–540 Ma range from impingement of multiple mantle plumes to rifting activity linked to the breakout of the Laurentian plate from the Rodinia supercontinent configuration. We add to the debate about the origin of kimberlite magmas and evaluate possible mantle sources of the 655 Ma ‘diamond-rich’ Renard (new SIMS U/Pb perovskite ages) and 629 Ma ‘barren’ Wemindji kimberlites on the eastern Superior craton in Quebec, Canada. Our Sr-Nd-Hf and carbon isotope data (87Sr/86Sri = 0.70241–0.70442; ?Ndi = + 0.2 to + 4.8; ?Hfi = + 0.3 to + 6.5; ?13C = ? 5.6 to ? 3.9‰) suggest a common and moderately depleted convecting upper mantle source region for both the Renard and Wemindji kimberlites, which occur 400 km apart in the interior of the Superior craton. In contrast, the low Os isotope ratios (187Os/188Osi = 0.11078–0.12620; ?Osi = ? 13.7 to ? 1.6) and unfractionated chondritic relative HSE abundances (Os, Ir, Ru, Pt, Pd, Re) indicate significant involvement of ancient refractory cratonic mantle material in kimberlite magma formation. Our model calculations suggest that for both the diamond-rich Renard and the barren Wemindji kimberlite magmas up to 30% of the Os was derived from refractory cratonic peridotites. This material might have been assimilated by originally more CO2-rich carbonated silicate melts derived from the asthenosphere. We also show that the geochemical and Sr-Nd-Hf-Os isotopic compositions of the Renard and Wemindji kimberlites do not require significant input from melts derived from olivine-poor cratonic mantle lithologies such as MARID-type veins and pyroxenites/eclogites. This contrasts with the petrogenesis of deeply-derived volatile-rich potassic magmas found along the peripheries of cratons (e.g., ultramafic lamprophyres, kamafugites, and olivine lamproites), a setting where abundant non-peridotitic components have been added to the lithospheric mantle over the course of continent evolution. Provided that CO2-rich melts, such as proto-kimberlites, occur near the solidus of volatile-fluxed peridotites, no excess mantle heat is required in their formation. This important but often overlooked constraint, together with the observation that there exist no spatial or temporal relationships between the Superior craton kimberlites and Large Igneous Provinces during the Late Neoproterozoic, suggests that kimberlite magmatic activity was tectonically controlled. In our preferred model, ubiquitous CO2-rich proto-kimberlite melts form during volatile-controlled redox melting processes at ambient mantle temperatures in a thermal boundary layer directly beneath thick cratonic lithosphere. The success rate of ‘evolving’ hybrid kimberlite magmas reaching Earth’s surface increases when tensile stresses propagate into the > 200 km thick keels of continental lithosphere. These conditions are frequently met during fast and changing plate motions associated with the assembly and breakup of supercontinents.
Abstract: The abundance and distribution of halogens (F, Cl) are rarely recorded in kimberlites and therefore their petrogenetic significance is poorly constrained. Halogens are usually present in kimberlite rocks in the structure of phlogopite and apatite, but their original concentrations are never fully retained due to the effects of alteration. To provide new constraints on the origin and evolution of halogens in kimberlites and their melts, we present a detailed study of the petrography and geochemistry of the late-Cretaceous Group-I (or archetypal) Roger kimberlite (Ekati cluster, Canada). The studied samples contain abundant anhedral-to-euhedral olivine which is set in a crystalline groundmass of monticellite, phlogopite, apatite, spinel (i.e. magnesian ulvöspinel-magnetite (MUM), Mg-magnetite, pleonaste, Cr-spinel), and perovskite along with abundant secondary alteration phases (i.e. serpentine, garnet (andradite-schlorlomite), amakinite ((Fe2 +, Mg, Mn)(OH)2), calcite). The Roger kimberlite is characterised by the highest recorded F-content (up to 2688 ppm) of the Ekati cluster kimberlites, which is reflected by the preservation of F-rich phases, where bultfonteinite (Ca4(Si2O7)(F, OH)2) and fluorite commonly replace olivine. In order to examine the composition and evolution of the kimberlite melt prior to post-magmatic processes, we studied melt inclusions in olivine, Cr-spinel, monticellite and apatite. Primary multiphase melt inclusions in Cr-spinel, monticellite and apatite and secondary inclusions in olivine are shown to contain a diversity of daughter phases and compositions that are dominated by alkali/alkali-earth (Na, K, Ba, Sr)-enriched Ca-Mg-carbonates ± F, Na-K-chlorides and sulphates, phosphates ± REE, spinel, silicates (e.g. olivine, phlogopite, (clino)humite), and sulphides. Although alkali/alkali-earth- and halogen-bearing phases are abundant in melt inclusions, they are generally absent from the kimberlite groundmass, most likely due to ubiquitous effects of syn- and/or post-magmatic alteration (i.e. serpentinisation). Comparisons between halogens and other trace elements of similar compatibility (i.e. F/Nd and Cl/U) in the Roger kimberlite and their respective estimated primitive mantle abundances show that halogens should be a more significant component in kimberlites than typically measured. We propose that fluorine in the Roger kimberlite was magmatic and was redistributed during hydrothermal alteration by Ca-bearing serpentinising fluids to produce the observed bultfonteinite/fluorite assemblages. Based the compositions and daughter mineral assemblages in primary melt inclusions and reconstructed halogen abundances, we suggest that Cr-spinel, monticellite and apatite crystallised from a variably differentiated Si-P-Cl-F-bearing carbonate melt that was enriched in alkalis/alkali-earths and highly incompatible trace elements.
Abstract: The abundance and distribution of halogens (F, Cl) are rarely recorded in kimberlites and therefore their petrogenetic significance is poorly constrained. Halogens are usually present in kimberlite rocks in the structure of phlogopite and apatite, but their original concentrations are never fully retained due to the effects of alteration. To provide new constraints on the origin and evolution of halogens in kimberlites and their melts, we present a detailed study of the petrography and geochemistry of the late-Cretaceous Group-I (or archetypal) Roger kimberlite (Ekati cluster, Canada). The studied samples contain abundant anhedral-to-euhedral olivine which is set in a crystalline groundmass of monticellite, phlogopite, apatite, spinel (i.e. magnesian ulvöspinel-magnetite (MUM), Mg-magnetite, pleonaste, Cr-spinel), and perovskite along with abundant secondary alteration phases (i.e. serpentine, garnet (andradite-schlorlomite), amakinite ((Fe2 +, Mg, Mn)(OH)2), calcite). The Roger kimberlite is characterised by the highest recorded F-content (up to 2688 ppm) of the Ekati cluster kimberlites, which is reflected by the preservation of F-rich phases, where bultfonteinite (Ca4(Si2O7)(F, OH)2) and fluorite commonly replace olivine. In order to examine the composition and evolution of the kimberlite melt prior to post-magmatic processes, we studied melt inclusions in olivine, Cr-spinel, monticellite and apatite. Primary multiphase melt inclusions in Cr-spinel, monticellite and apatite and secondary inclusions in olivine are shown to contain a diversity of daughter phases and compositions that are dominated by alkali/alkali-earth (Na, K, Ba, Sr)-enriched Ca-Mg-carbonates ± F, Na-K-chlorides and sulphates, phosphates ± REE, spinel, silicates (e.g. olivine, phlogopite, (clino)humite), and sulphides. Although alkali/alkali-earth- and halogen-bearing phases are abundant in melt inclusions, they are generally absent from the kimberlite groundmass, most likely due to ubiquitous effects of syn- and/or post-magmatic alteration (i.e. serpentinisation). Comparisons between halogens and other trace elements of similar compatibility (i.e. F/Nd and Cl/U) in the Roger kimberlite and their respective estimated primitive mantle abundances show that halogens should be a more significant component in kimberlites than typically measured. We propose that fluorine in the Roger kimberlite was magmatic and was redistributed during hydrothermal alteration by Ca-bearing serpentinising fluids to produce the observed bultfonteinite/fluorite assemblages. Based the compositions and daughter mineral assemblages in primary melt inclusions and reconstructed halogen abundances, we suggest that Cr-spinel, monticellite and apatite crystallised from a variably differentiated Si-P-Cl-F-bearing carbonate melt that was enriched in alkalis/alkali-earths and highly incompatible trace elements
Abstract: The abundance and distribution of halogens (F, Cl) are rarely recorded in kimberlites and therefore their petrogenetic significance is poorly constrained. Halogens are usually present in kimberlite rocks in the structure of phlogopite and apatite, but their original concentrations are never fully retained due to the effects of alteration. To provide new constraints on the origin and evolution of halogens in kimberlites and their melts, we present a detailed study of the petrography and geochemistry of the late-Cretaceous Group-I (or archetypal) Roger kimberlite (Ekati cluster, Canada). The studied samples contain abundant anhedral-to-euhedral olivine which is set in a crystalline groundmass of monticellite, phlogopite, apatite, spinel (i.e. magnesian ulvöspinel-magnetite (MUM), Mg-magnetite, pleonaste, Cr-spinel), and perovskite along with abundant secondary alteration phases (i.e. serpentine, garnet (andradite-schlorlomite), amakinite ((Fe2 +, Mg, Mn)(OH)2), calcite). The Roger kimberlite is characterised by the highest recorded F-content (up to 2688 ppm) of the Ekati cluster kimberlites, which is reflected by the preservation of F-rich phases, where bultfonteinite (Ca4(Si2O7)(F, OH)2) and fluorite commonly replace olivine. In order to examine the composition and evolution of the kimberlite melt prior to post-magmatic processes, we studied melt inclusions in olivine, Cr-spinel, monticellite and apatite. Primary multiphase melt inclusions in Cr-spinel, monticellite and apatite and secondary inclusions in olivine are shown to contain a diversity of daughter phases and compositions that are dominated by alkali/alkali-earth (Na, K, Ba, Sr)-enriched Ca-Mg-carbonates ± F, Na-K-chlorides and sulphates, phosphates ± REE, spinel, silicates (e.g. olivine, phlogopite, (clino)humite), and sulphides. Although alkali/alkali-earth- and halogen-bearing phases are abundant in melt inclusions, they are generally absent from the kimberlite groundmass, most likely due to ubiquitous effects of syn- and/or post-magmatic alteration (i.e. serpentinisation). Comparisons between halogens and other trace elements of similar compatibility (i.e. F/Nd and Cl/U) in the Roger kimberlite and their respective estimated primitive mantle abundances show that halogens should be a more significant component in kimberlites than typically measured. We propose that fluorine in the Roger kimberlite was magmatic and was redistributed during hydrothermal alteration by Ca-bearing serpentinising fluids to produce the observed bultfonteinite/fluorite assemblages. Based the compositions and daughter mineral assemblages in primary melt inclusions and reconstructed halogen abundances, we suggest that Cr-spinel, monticellite and apatite crystallised from a variably differentiated Si-P-Cl-F-bearing carbonate melt that was enriched in alkalis/alkali-earths and highly incompatible trace elements
Abstract: The abundance and distribution of halogens (F, Cl) are rarely recorded in kimberlites and therefore their petrogenetic significance is poorly constrained. Halogens are usually present in kimberlite rocks in the structure of phlogopite and apatite, but their original concentrations are never fully retained due to the effects of alteration. To provide new constraints on the origin and evolution of halogens in kimberlites and their melts, we present a detailed study of the petrography and geochemistry of the late-Cretaceous Group-I (or archetypal) Roger kimberlite (Ekati cluster, Canada). The studied samples contain abundant anhedral-to-euhedral olivine which is set in a crystalline groundmass of monticellite, phlogopite, apatite, spinel (i.e. magnesian ulvöspinel-magnetite (MUM), Mg-magnetite, pleonaste, Cr-spinel), and perovskite along with abundant secondary alteration phases (i.e. serpentine, garnet (andradite-schlorlomite), amakinite ((Fe2 +, Mg, Mn)(OH)2), calcite). The Roger kimberlite is characterised by the highest recorded F-content (up to 2688 ppm) of the Ekati cluster kimberlites, which is reflected by the preservation of F-rich phases, where bultfonteinite (Ca4(Si2O7)(F, OH)2) and fluorite commonly replace olivine. In order to examine the composition and evolution of the kimberlite melt prior to post-magmatic processes, we studied melt inclusions in olivine, Cr-spinel, monticellite and apatite. Primary multiphase melt inclusions in Cr-spinel, monticellite and apatite and secondary inclusions in olivine are shown to contain a diversity of daughter phases and compositions that are dominated by alkali/alkali-earth (Na, K, Ba, Sr)-enriched Ca-Mg-carbonates ± F, Na-K-chlorides and sulphates, phosphates ± REE, spinel, silicates (e.g. olivine, phlogopite, (clino)humite), and sulphides. Although alkali/alkali-earth- and halogen-bearing phases are abundant in melt inclusions, they are generally absent from the kimberlite groundmass, most likely due to ubiquitous effects of syn- and/or post-magmatic alteration (i.e. serpentinisation). Comparisons between halogens and other trace elements of similar compatibility (i.e. F/Nd and Cl/U) in the Roger kimberlite and their respective estimated primitive mantle abundances show that halogens should be a more significant component in kimberlites than typically measured. We propose that fluorine in the Roger kimberlite was magmatic and was redistributed during hydrothermal alteration by Ca-bearing serpentinising fluids to produce the observed bultfonteinite/fluorite assemblages. Based the compositions and daughter mineral assemblages in primary melt inclusions and reconstructed halogen abundances, we suggest that Cr-spinel, monticellite and apatite crystallised from a variably differentiated Si-P-Cl-F-bearing carbonate melt that was enriched in alkalis/alkali-earths and highly incompatible trace elements
Abstract: Monticellite is a magmatic and/or deuteric mineral that is often present, but widely varying in concentrations in Group-I (or archetypal) kimberlites. To provide new constraints on the petrogenesis of monticellite and its potential significance to kimberlite melt evolution, we examine the petrography and geochemistry of the minimally altered hypabyssal monticellite-rich Leslie (Canada) and Pipe 1 (Finland) kimberlites. In these kimberlites, monticellite (Mtc) is abundant (25–45 vol%) and can be classified into two distinct morphological types: discrete and intergrown groundmass grains (Mtc-I), and replacement of olivine (Mtc-II).
Monticellite in group-I kimberlites: Implications for evolution of parental melts and post-emplacement CO 2 degassing (PDF Download Available).
Abstract: Monticellite is a magmatic and/or deuteric mineral that is often present, but widely varying in concentrations in Group-I (or archetypal) kimberlites. To provide new constraints on the petrogenesis of monticellite and its potential significance to kimberlite melt evolution, we examine the petrography and geochemistry of the minimally altered hypabyssal monticellite-rich Leslie (Canada) and Pipe 1 (Finland) kimberlites. In these kimberlites, monticellite (Mtc) is abundant (25–45 vol%) and can be classified into two distinct morphological types: discrete and intergrown groundmass grains (Mtc-I), and replacement of olivine (Mtc-II).
Monticellite in group-I kimberlites: Implications for evolution of parental melts and post-emplacement CO 2 degassing (PDF Download Available).
Abstract: A suite of 17 unique big (1 to 20 kg) and fresh ecligite xenoliths from Udachnaya kimberlite pipe have been studied for their whole-rock and minerals major and trace elements composition.Whole rock major elements composition of the Udachnaya eclogite xenoliths suite have a great variability in their MgO contents (9-19Wt%). Based on major elements composition Udachnaya eclogites can be subdivided in two subsets, high magnesian (Mg# 68.8-81.9) and low magnesian (Mg# 56.8-59). High variations also shown by Al2O3 and Na2O concentrations and high Mg# samples tend to contain less of those oxides then low Mg# samples with some exceptions. Two eclogitic groups are clearly different in style of inter-elements correlations. FeO and CaO contents are positively correlate with MgO in low Mg# group of eclogites but negatively in high Mg# group. The same relations present between Al2O3 contents of eclogite group with their Mg#. Compared to present day MORB composition eclogite samples have similar contents of most of elements with some depletion in TiO2 and P2O5 and enrichment in MgO and K2O. The variability of these elements concentrations can be related to melt extraction while elevated K2O can indicate late metasomatic enrichment. In terms of trace elements composition Udachnaya eclogites are enriched over PM but comparable to that of MORB composition, except significant enrichment in LILE elements (Rb, Ba, K, Sr). The records of both subduction related processes and mantle metasomatism could be find in geochemical features of these rocks. Most of the eclogites show positive Eu anomaly which is direct evidence of plagioclase accumulation in eglogites protolith. Variation of La/Yb ratio (1-11), in majority of samples are the range 2-4 indicates different degrees of samples metasomatic enrichment in LREE. Udachnaya eclogites have range of Sm/Nd ratio from 0.25 to 0.5 (MORB is 0.32) which positive covariates with Nd content. This trend could not be a result of melt extraction nor metasomatic enrichment rather it could reflect heterogeneity of oceanic crust composition and/or mixing with peridotite component during subduction.
Abstract: The Karowe mine, owned and operated by Lucara Diamond Corporation, located in the Republic of Botswana, achieved commercial diamond production in July 2012. The AK06 kimberlite discovered in 1969 is the ore source at Karowe. The AK06 kimberlite within the Orapa Kimberlite Field is a roughly north-south elongate kimberlite body with a near surface expression of approximately 3.3 ha and a maximum area of approximately 7 ha at approximately 120 m below surface. The body comprises three geologically distinct, coalescing pipes that taper with depth. These pipes are referred to as the North Lobe, Centre Lobe, and South Lobe. The AK6 kimberlite is an opaque-mineral-rich monticellite kimberlite, texturally classified primarily as fragmental volcaniclastic kimberlite with lesser macrocrystic hypabyssal facies kimberlite of the Group 1 variety. The nature of the kimberlite differs between each lobe with distinctions apparent in the textural characteristics. The South Lobe is considered to be distinctly different from the North and Centre Lobes that are similar to each other in terms of their geological characteristics. The North and Centre Lobes exhibit internal textural complexity whereas the bulk of the South Lobe is more massive and internally homogeneous. The South Lobe forms the majority of the resource and displays the coarsest diamond size distribution of the three lobes. In three years of production, Karowe has established a continuing production of high value diamonds including coloured diamonds. In March 2013 a 239 ct gem quality diamond was recovered which was the first in a continuing population of large high value Type IIa diamonds recovered from the Centre Lobe, and more importantly the South Lobe, of the Karowe mine. Large diamonds, 50 ct in size, are spatially distributed horizontally and vertically within the South Lobe. Since commissioning to mid-December 2015, approximately 1.5 Mct have been produced and specials (diamonds greater than 10.8 ct in weight) represent circa 4.6% by weight of all diamond production. Life of Mine average stone size for the specials is 29.6 ct/stone. In 2015, a plant optimization project was completed to modify the process plant to treat harder kimberlite at depth and improve the recovery of exceptional diamonds via bulk sorters for primary run of mine large diamond recovery. In November 2015, the Karowe mine recovered an 813 ct stone and the world’s second largest gem quality diamond in over 100 years weighing 1,111 ct
Formation of dunite xenoliths in kimberlites and allikites, petrographic and mineral compositions from a deformed xenolith in the Majuagaa kimberlite dike, Greenland.
Re-Os isotope systematics of sulphide inclusions in diamonds from Victor ( Superior craton) document mobilization of volatiles and Os during Rodinia break up.
Abstract: The Kennady North Project kimberlites are located approximately 280 kilometers east-northeast of Yellowknife, in the Northwest Territories of Canada. The unusual geometry and extent of the kimberlite magmatic system is revealed by renewed exploration drilling activities by Kennady Diamonds since 2012. It has become clear that the system comprises multiple intrusive dykes within which several volcaniclastic bodies have developed, all within 11 kilometres of the Gahcho Kué kimberlite cluster and diamond mine. The detailed exploration of the entire system provides unique evidence for subterranean volcanic conduit growth processes that may have scientific and practical exploration benefits.
Abstract: The Kennady North Project kimberlites are located approximately 280 kilometers east-northeast of Yellowknife, in the Northwest Territories of Canada. The unusual geometry and extent of the kimberlite magmatic system is revealed by renewed exploration drilling activities by Kennady Diamonds since 2012. It has become clear that the system comprises multiple intrusive dykes within which several volcaniclastic bodies have developed, all within 11 kilometres of the Gahcho Kué kimberlite cluster and diamond mine. The detailed exploration of the entire system provides unique evidence for subterranean volcanic conduit growth processes that may have scientific and practical exploration benefits.
Density measurement within the context of the rock mass characterization program of the Kelvin and Faraday kimberlites and surrounding country rock in the Northwest Territories of Canada.
Density measurement within the context of the rock mass characterization program of the Kelvin and Faraday kimberlites and surrounding country rock in the Northwest Territories of Canada.
Cr-rich megacrysts of clinopyroxene and garnet from Lac de Gras kimberlites, Slave craton, Canada - implications for the origin of clinopyroxenes and garnet in cratonic peridotites.
Abstract: Megacrystic (>1 cm) clinopyroxene (Cr-diopside) and garnet (Cr-pyrope) xenocrysts within kimberlites from Lac de Gras (Northwest Territories, Canada) contain fully crystallized melt inclusions. These `polymineralic inclusions' have previously been interpreted to form by necking down of melts at mantle depths. We present a detailed petrographical and geochemical investigation of polymineralic inclusions and their host crystals to better understand how they form and what they reveal about the evolution of kimberlite melt. Genetically, the megacrysts are mantle xenocrysts with peridotitic chemical signatures indicating an origin within the lithospheric mantle (for the Cr-diopsides studied here ~4.6 GPa, 1015 °C). Textural evidence for disequilibrium between the host crystals and their polymineralic inclusions (spongy rims in Cr-diopside, kelyphite in Cr-pyrope) is consistent with measured Sr isotopic disequilibrium. The preservation of disequilibrium establishes a temporal link to kimberlite eruption. In Cr-diopsides, polymineralic inclusions contain phlogopite, olivine, chromite, serpentine, and calcite. Abundant fluid inclusion trails surround the inclusions. In Cr-pyropes, the inclusions additionally contain Al-spinel, clinopyroxene, and dolomite. The major and trace element compositions of the inclusion phases are generally consistent with the early stages of kimberlite differentiation trends. Extensive chemical exchange between the host phases and the inclusions is indicated by enrichment of the inclusions in major components of the host crystals, such as Cr2O3 and Al2O3. This chemical evidence, along with phase equilibria constraints, supports the proposal that the inclusions within Cr-diopside record the decarbonation reaction: dolomitic melt + diopside ? forsterite + calcite + CO2, yielding the observed inclusion mineralogy and producing associated (CO2-rich) fluid inclusions. Our study of polymineralic inclusions in megacrysts provides clear mineralogical and chemical evidence for an origin of kimberlite that involves the reaction of high-pressure dolomitic melt with diopside-bearing mantle assemblages producing a lower-pressure melt that crystallizes a calcite-dominated assemblage in the crust.
Geochemical and petrographical study of megacrysts and mantle xenoliths from Gemsbok Hollow and Gruendorn kimberlites in the Warmbad kimberlite Province, South Africa
Geochemistry and geothermobarometry of lherzolite and pyroxenite xenoliths from the CH-33, CH-52 & CH-58 Diamondiferous kimberlite pipes at Chidliak ( Baffin Island, Canada).
Geochemistry and geothermobarometry of lherzolite and pyroxenite xenoliths from the CH-33, CH-52 & CH-58 Diamondiferous kimberlite pipes at Chidliak ( Baffin Island, Canada).
Geochemistry and geothermobarometry of lherzolite and pyroxenite xenoliths from the CH-33, CH-52 & CH-58 Diamondiferous kimberlite pipes at Chidliak ( Baffin Island, Canada).
The Canadian Mineralogist, Vol. 55, 4, pp. 521-533.
Technology
Deposit - Renard 2
Abstract: The purpose of this work is to investigate the crystal growth parameters necessary or sufficient to obtain a crystal specifically of gem quality. We assume adequate chemistry is available. First, nucleation must occur with only a limited number of nuclei, otherwise too many crystals will be produced, and they will be too small to be faceted into a gem. Two growth mechanisms are readily documented for gems: Most commonly there is slow growth, driven by a spiral growth mechanism, leading to large single individuals. There are only a few examples of fast growth leading to gem-quality edifices: examples include “gota de aceite” Colombian emerald or the dendritic “pseudo cube” for gem diamonds. We have not documented the intermediate conditions between these two extremes in the Sunagawa diagram, which would correspond to 2D nucleation growth. The presence of inclusions is to be limited to desirable ones. Thus, in general, a good stability of the growth interface is the best guarantee of good clarity in the final gem. As for the interface, in general, growth conditions must be relatively stable over the period necessary to achieve growth. Perhaps surprisingly, it has become well documented that gem-quality near-colorless diamonds may have experienced quite a complex growth history. Therefore, the term stability has to be re-defined for each system producing a given gem. The length of time it takes to achieve crystallization of the gem has rarely been studied or estimated. Scientific evidence from experimental petrology and the growth of synthetic gems indicates that it does not take millions of years to grow a gem, but that this exercise may be achieved in a week to, arguably, a few years at the most. Available free space to grow does not appear always necessary, but it helps. Otherwise deformation, inclusions, and other negative effects may occur. Finally, no dramatic post-growth events, such as fracturing or etching, should affect the gem crystal.
Slope stability challenges and solutions for mining kimberlite resources hosted in structurally complex country rock: dip slope mining at Jwaneng mine, Botswana.
Abstract: The Renard 65 pipe is located in the Otish Mountains, Quebec, Canada. It is one of nine diamondiferous kimberlite pipes in the ~ 640 Ma Renard cluster and is the largest of four pipes in the Renard Mine reserve. Detailed characterizations of the petrographic and compositional features of these pipe-infilling kimberlite rock types supports their classification into three geological units: Kimb65a, Kimb65b, and Kimb65d. These pipe-infilling kimberlites are interpreted to represent the solidified products of two separate magmatic events: Phase A containing Kimb65a, and Phase B containing Kimb65b and Kimb65d. This research demonstrates that the interclast matrix modal mineralogy (diopside + phlogopite + serpentine) in pyroclastic rock types in the Renard 65 kimberlites are inconsistent with origins by hydrothermal alteration involving hydrous meteoric fluids. Detailed investigation of the reactions between granitic and gneissic crustal xenolith lithologies and their host kimberlites, suggests that reactions occur at both magmatic and subsolidus temperatures involving significant volumetric proportions of xenoliths. The assimilation of crustal xenoliths, and contamination of the kimberlite magmas primarily by Si, are demonstrated to result in enhanced degassing of magmatic volatiles during emplacement and stabilization of the hybrid groundmass assemblage diopside + phlogopite + serpentine over the non hybrid groundmass assemblage calcite + phlogopite + serpentine. It is thus interpreted that the spatial distribution of transitional to Kimberley-type pyroclastic kimberlite rock types, which are characterized by diopside-rich and calcite-poor matrix assemblages as observed in the Renard 65 pipe and other similar pipes, is a function of crustal xenolith distribution in the magma during emplacement. This model not only accounts for the features of Kimberley-type pyroclastic kimberlite rock types, but also the spatial distribution of these rock types in numerous pipes which is often not consistent with lateral textural gradations as has been previously proposed. These results further indicate that the different mineralogy and textures of Fort-à-la-Corne-type pyroclastic kimberlites with respect to Kimberley-type pyroclastic kimberlites may be a consequence of not only the structural controls imparted by the host rock lithology with implications for emplacement-related processes, but also the absence of contamination of the magma by silicic crustal xenoliths.
Subsolidus compositional modification of kimberlitic spinel in the Renard 65 kimberlite pipe, Quebec, Canada - implications for the use of spinel chemistry in the identification of kimberlite phases.
Tracing mantle metasomatism using combined stable (S,O) and radiogenic (Sr, Nd, Hf, Pb) isotope geochemistry: case studies from mantle xenoliths of the Kimberley kimberlites.
Abstract: The diamondiferous Letlhakane kimberlites are part of the Orapa kimberlite cluster (˜ 93.1 Ma) in north-eastern Botswana, located on the edge of the Zimbabwe Craton, close to the Proterozoic Magondi Mobile Belt. Here we report the first Re-Os ages of six individual eclogitic sulphide inclusions (3.0 to 35.7?g) from Letlhakane diamonds along with their rhenium, osmium, iridium and platinum concentrations, and carbon isotope, nitrogen content and N-aggregation data from the corresponding growth zones of the host diamonds. For the first time, Re-Os data will be compared to Sm-Nd ages of individual eclogitic silicate inclusions recovered from the same diamonds using a Triton Plus equipped with four 1013? amplifiers. The analysed inclusion set currently encompasses pairs of individual sulphides from two diamonds (LK040 sf4 & 5, LK113 sf1 & 2) and two sulphide inclusions from separate diamonds (LK048, LK362). Ongoing work will determine the Sm-Nd ages and element composition of multiple individual eclogitic garnets (LK113/LK362, n=4) and an eclogitic clinopyroxene (LK040) inclusion. TMA ages of the six sulphides range from 1.06 to 2.38 Ga (± 0.1 to 0.54 Ga) with Re and Os contents between 7 and 68 ppb and 0.03 and 0.3 ppb, respectively. The host diamond growth zones have low nitrogen abundances (21 to 43 ppm N) and high N-aggregation (53 to 90% IaB). Carbon isotope data suggests the involvement of crustal carbon (?13C between -19.3 to -22.7 ± 0.2 per mill) during diamond precipitation. Cathodoluminescence imaging of central plates from LK040 and LK113 displays homogenous internal structure with no distinct zonation. The two sulphide inclusions from LK040 define an 'isochron' of 0.92 ± 0.23 Ga (2SD) with initial 187Os/188Os = 1.31 ± 0.24. Sulphides from LK113 have clear imposed diamond morphology and indicate diamond formation at 0.93 ± 0.36 Ga (2SD) with initial 187Os/188Os = 0.69 ± 0.44. The variation in the initial 187Os/188Os does not justify including these inclusions (or any from other diamonds) on the same isochron and implies an extremely heterogeneous diamond crystallisation environment that incorporated recycled Os. C1-normalized osmium, iridium and platinum (PGE) compositions from the analysed sulphide inclusions display enrichment in Ir (3.4 to 33) and Pt (2.3 to 28.1) in comparison to eclogitic xenolith data from Orapa that are depleted relative to chondrite. The Re-Os isochrons determined in this study are within error of previously reported ages from the adjacent (˜40km) Orapa diamond mine (1.0 to 2.9 Ga) based on sulphide inclusions and a multi-point 990 ± 50 Ma (2SD) isochron for composite (n=730) silicate inclusions. Together with additional new Sm-Nd isochron age determinations from individual silicate inclusions from Letlhakane (2.3 ± 0.02 (n = 3); 1.0 ± 0.14 (n = 4) and 0.25 ± 0.04 Ga (n = 3), all 2SE) these data suggest a phase of Mesoproterozoic diamond formation as well as Neoarchean/Paleoproterozoic and Mesozoic diamond growth, in punctuated events spanning >2.0 Ga.
Tracing kimberlitic indicators to their kimberlite source at Chidliak, Nunavut, Canada, re-visited: the unexpected accuracy of a simplified Mahalanobis-distance approach.
Abstract: The Rae craton in Canada’s North contains several kimberlite fields and has been the subject of episodic diamond exploration, with proven diamond-bearing deposits. However, relatively little is known about the deep mantle lithosphere that underpins the architecturally complex crust of this craton. The Darby Kimberlite field, located ~120 km southwest of the community of Kugaaruk, Nunavut, provides an opportunity to study the mantle beneath the western portion of the central Rae craton via mantle xenoliths. The Darby kimberlite field contains eight kimberlite bodies erupted at circa 540 Ma. Five of the kimberlites have proven to be diamond-bearing including the 12 hectare ‘Iceberg’ kimberlite. Mantle xenoliths were collected from kimberlite float above proven kimberlite targets across the property. Most of the surface kimberlite is highly altered and hence the peridotite xenoliths they contain are generally serpentinized or deeply-weathered. Eclogites/pyroxenites were recovered from each locality visited. A total of 33 mantle xenoliths exceeding one cm in maximum dimension (14 peridotites and 19 “eclogites”) were selected for mineral chemistry and bulk analysis. Four peridotite xenoliths contain fresh garnet. Clinopyroxenes from kimberlite heavy mineral concentrate provide a preliminary geotherm for the West Central Rae lithosphere and indicate a lithospheric depth of ~200 km. Using Ni-in-garnet temperatures, four garnet peridotites and 49 peridotitic garnets from concentrate yield two distinct mantle sampling depths. Whole rock Re-depletion ages for Darby peridotites range from Mesoarchean to Paleoproterozoic. Archean whole rock TMA ages for the eclogites/pyroxenites are consistent with a Mesoarchean age for the western Central Rae lithosphere, older than the lithosphere beneath the Repulse Bay block to the East. The anomalously high abundance of eclogite/pyroxenite xenoliths and garnet concentrate found in the Darby field (58 % of xenoliths and 82 % of concentrate) is at odds with the abundance of eclogite thought to be present in cratonic lithospheric mantle from xenocryst studies (~one to five %). The high abundance may be related to the proximity of the field to the proposed suture between the Committee Block and the Queen Maud Block to the far West of the Rae craton
Abstract: The Letšeng Diamond Mine comprises two adjacent kimberlites, the Main and Satellite pipes. Very low grade and low frequency of high value stones preclude use of standard evaluation methods, increasing the need for high confidence geology models. New results of drillcore investigations, including core logging, country rock dilution measurements, indicator mineral abundances and petrography are integrated with open pit mapping and macrodiamond production data to present updated 3D geological models of the Main and Satellite pipes. Letšeng was emplaced ~90 Ma and forms part of a Cretaceous kimberlite province extending across southern Africa. The Letšeng bodies are steep-sided volcanic pipes that are infilled with multiple asymmetric phases of kimberlite separated by near-vertical, sharp, cross-cutting internal contacts. There are associated marginal carbonate-cemented country-rock breccias and sub-vertical kimberlite dykes that can occur within a zone of well-developed carbonate veining adjacent to the pipes. The pipe infills are dominated by kimberlite closely resembling Kimberley-type pyroclastic kimberlite (KPK; formerly tuffisitic kimberlite; Scott Smith et al. 2013) that contains common large megaxenoliths of massive and brecciated country rock basalt. Other textural varieties include hypabyssal kimberlite (HK), transitional HK-KPK and resedimented volcaniclastic kimberlite (RVK). Each phase of kimberlite represents a separate magmatic system. In each KPK there is a continuum of crystallization from the magmaclast selvages to the intermagmaclast matrix. As documented elsewhere, the HK-KPK transition involves an increasing (i) degree of deuteric replacement of olivine, (ii) amount of incorporated country rock xenoliths and (iii) textural modification of the magma prior to solidification subsurface within the diatreme. These conclusions negate some other proposed modes of emplacement.
Abstract: An oceanic crustal origin is the commonly accepted paradigm for mantle-derived eclogites. However, the significance of the aluminous members of the eclogite suite, containing kyanite and corundum, has long been underrated and their role neglected in genetic models of cratonic evolution. Here, we present a geochemical and petrological study of a suite of kyanite- and corundum-bearing eclogites from the Bellsbank kimberlite, S. Africa, which originate from depths between 150 and 200 km. Although clearly of high-pressure provenance, these rocks had a low-pressure cumulative origin with plagioclase and olivine as major cumulate phases. This is shown by the very pronounced positive Eu anomalies, low REE abundances, and ?18O values lower than the Earth’s mantle. Many chemical features are identical to modern-day troctolitic cumulates including a light REE depletion akin to MORB, but there are also distinguishing features in that the eclogites are richer in Na, Fe, and Ni. Two of the eclogites have a minimum age of ~3.2 Ga, defined by the extremely unradiogenic 87Sr/86Sr (0.7007) in clinopyroxene. Phase equilibria indicate that the parent melts were formed by partial melting below an Archean volcanic center that generated (alkali-)picritic to high-alumina tholeiitic melts from a mantle whose oxygen fugacity was lower than today. Fractional crystallization produced troctolites with immiscible sulfide melt droplets within the mafic crust. Instability of the mafic crust led to deep subduction and re-equilibration at 4–6 GPa. Phase relationships plus the presence of a sample with appreciable modal corundum but no Eu anomaly suggest that kyanite- and corundum-bearing eclogites may also originate as plagioclase-free, higher pressure cumulates of highly aluminous clinopyroxene, spinel, and olivine. This is consistent with the crystallizing phase assemblage from an olivine tholeiitic to picritic magma deeper in the Archean oceanic crust or uppermost mantle. We postulate that the magmatic and subduction processes driving modern plate tectonics already existed in the Meso- to Early Archean.
Abstract: Kimberlites of the Udachnaya-East pipe (Siberia) include a uniquely dry and serpentine-free rock type with anomalously high contents of chlorine (Cl ? 6.1 wt%), alkalies (Na2O + K2O ? 10 wt%) and sulfur (S ? 0.50 wt%), referred to as a “salty” kimberlite. The straightforward interpretation is that the Na-, K-, Cl- and S-rich components originate directly from a carbonate-chloride kimberlitic magma that is anhydrous and alkali-rich. However, because brines and evaporites are present on the Siberian craton, previous studies proposed that the kimberlitic magma was contaminated by the assimilation of salt-rich crustal rocks. To clarify the origin of high Cl, alkalies and S in this unusual kimberlite, here we determine its sulfur speciation and isotopic composition and compare it to that of non-salty kimberlites and kimberlitic breccia from the same pipe, as well as potential contamination sources (hydrothermal sulfides and sulfates, country-rock sediment and brine collected in the area). The average ?34S of sulfides is ? 1.4 ± 2.2‰ in the salty kimberlite, 2.1 ± 2.7‰ in the non-salty kimberlites and 14.2 ± 5.8‰ in the breccia. The average ?34S of sulfates in the salty kimberlites is 11.1 ± 1.8‰ and 27.3 ± 1.6‰ in the breccia. In contrast, the ?34S of potential contaminants range from 20 to 42‰ for hydrothermal sulfides, from 16 to 34‰ for hydrothermal sulfates, 34‰ for a country-rock sediment (Chukuck suite) and the regional brine aquifer. Our isotope analyses show that (1) in the salty kimberlites, neither sulfates nor sulfides can be simply explained by brine infiltration, hydrothermal alteration or the assimilation of known salt-rich country rocks and instead, we propose that they are late magmatic phases; (2) in the non-salty kimberlite and breccia, brine infiltration lead to sulfate reduction and the formation of secondary sulfides – this explains the removal of salts, alkali-carbonates and sulfates, as well as the minor olivine serpentinization; (3) hydrothermal sulfur was added to the kimberlitic breccia, but not to the massive kimberlites. In situ measurements of sulfides confirm this scenario, clearly showing the addition of two sulfide populations in the breccia (pyrite-pyrrhotites with average ?34S of 7.9 ± 3.4‰ and chalcopyrites with average ?34S of 38.0 ± 0.4‰) whereas the salty and non-salty kimberlites preserve a unique population of djerfisherites (Cl- and K-rich sulfides) with ?34S values within the mantle range. This study provides the first direct evidence of alkaline igneous rocks in which magmatic sulfate is more abundant than sulfide. Although sulfates have been rarely reported in mantle materials, sulfate-rich melts may be more common in the mantle than previously thought and could balance the sulfur isotope budget of Earth's mantle.
Peridotite xenoliths of the Chidliak kimberlite province (NE Canada): The North Atlantic cratonic mantle with recent thermal and Ti-Na metasomatic disturbance.
Abstract: The Koffiefontein kimberlite is one of the classic locales on the Kaapvaal Craton and best known for being the first locality where very deep diamonds were recovered. Koffiefontein diamonds were last studied in 1980s and, based on major advances in micro-analytical techniques, here we revisit the mine to provide improved inclusion-based geothermobarometry. Currently, ~70 peridotitic diamonds have been studied with ~150 olivine, Cr-rich pyrope garnet, enstatite, and diopside inclusions liberated. So far, the inclusions were analysed (EPMA) for their major element compositions. The peridotitic inclusion suite is dominated by a highly-depleted harzburgitic association: olivine Mg-number ranges between 93 and 95, harzburgitic garnets contain < 3.00 wt % CaO, and 14 % of garnet inclusions are lherzolitic in paragenesis. Conventional mineral exchange geothermobarometry on non-touching inclusion pairs reveals that diamonds with harzburgitic inclusions derive from close to the base of the lithosphere (1143-1283 °C and 55-65 kbar; 12 diamonds) whilst much rarer lherzolitic inclusions last equilibrated in the upper portion of diamond stable lithosphere (983-1158 °C and 47-52 kbar; 5 diamonds). Both associations fall along a 39 mW/m2 reference geotherm (Hasterok and Chapman, 2011), implying a total lithosphere thickness of ~200 km at 90 Ma. To expand our geothermobarometry data beyond rare garnet-opx associations we conducted high-precision trace element analysis of Al and Ca in olivine inclusions via EPMA. Using long count times (300 sec on peak and each background) and a 200 nA beam current, detection limits of 8 ppm for Al and 6 ppm for Ca were achieved. This technique allowed for trace element analysis of olivine inclusions as small as 20 ?m in diameter. Based on these high-precision Al analyses, the updated Al-inolivine thermometer of Bussweiler et al (2017) extrapolated to a 39 mW/m2 geotherm yielded temperatures of 1124-1278 °C (30 diamonds).
Abstract: Kimberlites are volcanic ultramafic rocks originate from the upper mantle, and some are diamond bearing. Due to assimilation of mantle and crustal material, loss of volatiles, significant alteration and variable compositions of kimberlite seen at the surface, the primary composition and proportion of melt fluids (H2O, CO2) are unknown. Kimberlitic fluid and melt composition have significant effects on the preservation and quality of diamonds carried to the surface. In an attempt to gain predictive knowledge of the economic viability of a kimberlite, it is important to understand the primary and evolving compositions of kimberlite magmas, as well as the behaviour of volatiles during kimberlite eruption. Apatite is a common groundmass mineral in kimberlite, and has a composition sensitive to volatiles and trace elements [Ca5(PO4)3(F,Cl,OH)]. This study will examine the variation of apatite occurrence, composition, texture and trace element distribution in relation to varied kimberlite geologies and explore the potential of apatite as an indicator of fluid history and melt composition. Seven kimberlites have been selected for a study of groundmass apatite. The six Ekati property kimberlites (Koala, Misery, Panda, Beartooth, Leslie and Grizzly) have been chosen for their varying facies and styles of eruption. Panda and Beartooth are resedimented volcaniclastic kimberlites. Misery and Koala are massive volcaniclastic kimberlites. Leslie and Grizzly are pipe-fill coherent kimberlites. The seventh kimberlite, Snap Lake, is a coherent kimberlite dyke. All kimberlites are located in the Northwest Territories, Canada. Selecting kimberlites with diverse eruption styles allows us to test the apatite indicator model for a variety of potential volatile histories. Back scatter electron imaging has been used to identify and discriminate significant differences in apatite abundance and textural characteristics from Ekati kimberlites and Snap Lake. Wavelength dispersive spectroscopic analysis for major and some trace elements (LREE’s, Sr, Ba) reveals primary substitution mechanisms for rare earth element (REE) incorporation into apatite structure. Previous studies show that distribution of trace elements into apatite greatly depends on the growth media. Partitioning of the LREE’s relative to Sr is significantly different between silicate melt, carbonate melt, and aqueous fluid. Experimental partition coefficients between apatite and various growth media are used to test existing hypotheses of kimberlite melt composition. The future aim of this project is to establish apatite as an effective indicator of magmatic fluid and outline the applicability of groundmass apatite as an indicator of diamond preservation potential in kimberlites.
Abstract: Kimberlites are volcanic ultramafic rocks originate from the upper mantle, and some are diamond bearing. Due to assimilation of mantle and crustal material, loss of volatiles, significant alteration and variable compositions of kimberlite seen at the surface, the primary composition and proportion of melt fluids (H2O, CO2) are unknown. Kimberlitic fluid and melt composition have significant effects on the preservation and quality of diamonds carried to the surface. In an attempt to gain predictive knowledge of the economic viability of a kimberlite, it is important to understand the primary and evolving compositions of kimberlite magmas, as well as the behaviour of volatiles during kimberlite eruption. Apatite is a common groundmass mineral in kimberlite, and has a composition sensitive to volatiles and trace elements [Ca5(PO4)3(F,Cl,OH)]. This study will examine the variation of apatite occurrence, composition, texture and trace element distribution in relation to varied kimberlite geologies and explore the potential of apatite as an indicator of fluid history and melt composition. Seven kimberlites have been selected for a study of groundmass apatite. The six Ekati property kimberlites (Koala, Misery, Panda, Beartooth, Leslie and Grizzly) have been chosen for their varying facies and styles of eruption. Panda and Beartooth are resedimented volcaniclastic kimberlites. Misery and Koala are massive volcaniclastic kimberlites. Leslie and Grizzly are pipe-fill coherent kimberlites. The seventh kimberlite, Snap Lake, is a coherent kimberlite dyke. All kimberlites are located in the Northwest Territories, Canada. Selecting kimberlites with diverse eruption styles allows us to test the apatite indicator model for a variety of potential volatile histories. Back scatter electron imaging has been used to identify and discriminate significant differences in apatite abundance and textural characteristics from Ekati kimberlites and Snap Lake. Wavelength dispersive spectroscopic analysis for major and some trace elements (LREE’s, Sr, Ba) reveals primary substitution mechanisms for rare earth element (REE) incorporation into apatite structure. Previous studies show that distribution of trace elements into apatite greatly depends on the growth media. Partitioning of the LREE’s relative to Sr is significantly different between silicate melt, carbonate melt, and aqueous fluid. Experimental partition coefficients between apatite and various growth media are used to test existing hypotheses of kimberlite melt composition. The future aim of this project is to establish apatite as an effective indicator of magmatic fluid and outline the applicability of groundmass apatite as an indicator of diamond preservation potential in kimberlites.
Mineral inclusions in diamonds from Karowe mine, Botswana: examining the mantle sources of a diamond population containing exceptionally large crystals.
Abstract: Diamonds originating from the transition zone or lower mantle were previously identified based on the chemistry of their silicate or oxide mineral inclusions. Here we present data for such a super-deep origin based on the internal pressure of nitrogen in sub-micrometer inclusions in diamonds from Juina, Brazil. Infrared spectroscopy of four diamonds, rich in such inclusions revealed high concentrations of fully aggregated nitrogen (average of 900 ppm, all in B centers) and almost no platelets. Raman spectroscopy indicated the presence of solid, cubic ?-N2 at 10.9±0.2 GPa (corresponding to a density of 1900 kg/m3). Transmission electron microscopy of two diamonds found two generations of octahedral inclusions: microinclusions (average size: 150 nm, average concentration: 100 ppm) and nanoinclusions (20–30 nm, 350 ppm). EELS detected nitrogen and a diffraction pattern of one nanoinclusion yielded a tetragonal phase, which resembles ?-N2 with a density of 1400 kg/m3 (internal pressure = 2.7 GPa). We also observed up-warping of small areas (?150 nm in size) on the polished surface of one diamond. The ?2 nm rise can be explained by a shallow subsurface microinclusion, pressurized internally to more than 10 GPa. Using available equations of state for nitrogen and diamond, we calculated the pressures and temperatures of mechanical equilibrium of the inclusions and their diamond host at the mantle geotherm. The inclusions originated at the deepest part of the transition zone at pressures of ?22 GPa (630 km) and temperatures of ?1640?°C. We suggest that both generations are the result of exsolution of nitrogen from B centers and that growth took a few million years in a subducting mantle current. The microinclusions nucleated first, followed by the nanoinclusions. Shortly after the exsolution events, the diamonds were trapped in a plume or an ascending melt and were transported to the base of the lithosphere and later to the surface.
Geochemistry of peridotitic clinopyroxene from the Diamondiferous Mbuji-Mayi and Tshibwe kimberlites ( DRC): insight into the compositional and thermal state of the SCLM beneath the eastern Kasai craton.
A tale of two pipes: using whole rock geochemistry to see through alteration and contamination at the CH-6 & CH-7 kimberlites, Chidliak kimberlite province, Baffin Island, Nunavut.
Punctuated long lived emplacement history of kimberlites from the Renard cluster, Superior Province, Canada indicated by new high precision U-Pb groundmass perovskite dating.
Abstract: A mineralogical study of the hypabyssal facies, late Cretaceous macrocrystic pulse of TK1 intrusion and the Mesoproterozoic aphanitic pulse of TK4 intrusion in the Wajrakarur Kimberlite Field of southern India shows that the rocks contain macrocrysts of forsteritic olivine, phenocrysts and microphenocrysts of Al–Na-poor diopside and phlogopite set in a groundmass mainly of Al–Na-poor diopside and phlogopite. Other groundmass minerals are spinel, perovskite and fluorapatite in TK1, and spinel, titanite, chlorite, calcite and gittinsite in TK4. Krichterite and perovskite occur only as inclusions in phlogopite and titanite, respectively in TK4. Late-stage deuteric phases include pyrite and barite in TK1, and strontianite, chalcopyrite, galena and pentlandite in TK4. Diopside microphenocrysts in TK4 exhibit oscillatory zoning with characteristics of diffusion controlled magmatic growth. TK1 spinels show magmatic trend 2 that evolves from magnesiochromite and culminates in titaniferous magnetite, whereas TK4 spinels are less evolved with magnesiochromite composition only. TK1 phlogopites show a simple compositional trend that is typical of lamproite micas, while four distinct growth zones are observed in TK4 phlogopites with the following compositional characteristics: zone I: high Cr2O3 and TiO2 and low BaO; zone II: low Cr2O3; zone III: low TiO2 and high BaO; zone IV: low BaO. Forsterite contents and trace element concentrations reveal two xenocrystic core populations and one magmatic rim population for TK1 olivines. Mineralogically, both TK1 and TK4 are classified as diopside–phlogopite lamproites rather than archetypal kimberlites. The two lamproites are considered to have formed from the same parent magma but crystallised under distinct oxygen fugacity conditions. With elevated content of Fe3+ in phlogopite, spinel and perovskite, TK1 appears to have crystallised in a relatively high oxygen fugacity environment. Multiple growth generations of phlogopite, spinel and fluorapatite in TK4 indicate a complex evolutionary history of the magma. Close spatial and temporal associations of Mesoproterozoic kimberlites and lamproites in southern India can possibly be explained by a unifying model which accounts for the generation of diverse magmas from a range of geochemical resevoirs in a continental rift setting.
Abstract: Djerfisherite, a Cl-bearing potassium sulfide (K6Na(Fe,Ni,Cu)24S26Cl), is a widespread accessory mineral in kimberlite-hosted mantle xenoliths. Nevertheless, the origin of this sulfide in nodules remains disputable. It is usually attributed to the replacement of primary Fe–Ni–Cu sulfides when xenoliths interact with a K-and Cl-enriched hypothetical melt/fluid. The paper is devoted to a detailed study of the composition and morphology of djerfisherite from a representative collection (22 samples) of the deepest mantle xenoliths—sheared garnet peridotite, taken from the Udachnaya-East kimberlite pipe (Yakutia). Four types of djerfisherite were distinguished in the mantle rocks on the basis of morphology, spatial distribution, and relationships with the rock-forming and accessory minerals in the nodules. Type 1 was found in the rims of polysulfide inclusions in the rock-forming minerals of the xenoliths; there, it was younger than the primary sulfide assemblage pyrrhotite + pentlandite ± chalcopyrite. Type 2 formed rims around large polysulfide segregations (pyrrhotite+ pentlandite) in the xenolith interstices. Type 3 formed individual grains in the xenolith interstices together with other sulfides, silicates, oxides, phosphates, and carbonates. Type 4 was present as a daughter phase in the secondary melt inclusions which occurred in healed cracks in the rock-forming minerals of the xenoliths. Along with djerfisherite, the inclusions contained silicates, oxides, phosphates, carbonates, alkaline sulfates, chlorides, and sulfides. The results indicate that djerfisherite from the xenoliths is consanguine with kimberlite. Djerfisherite both in the sheared-peridotite xenoliths from the Udachnaya-East pipe and in different xenoliths from other kimberlite pipes worldwide formed owing to the interaction between the nodules and kimberlitic melts. Djerfisherite forming individual grains in the melt inclusions and xenolith interstices crystallized directly from the infiltrating kimberlitic melt. Djerfisherite bounding the primary Fe–Ni ± Cu sulfides formed by their replacement as a result of a reaction with the kimberlitic melt.
Abstract: The petrogenesis of kimberlites is commonly obscured by interaction with hydrothermal fluids, including deuteric (late-magmatic) and/or groundwater components. To provide new constraints on the modification of kimberlite rocks during fluid interaction and the fractionation of kimberlite magmas during crystallisation, we have undertaken a detailed petrographic and geochemical study of a hypabyssal sample (BK) from the Bultfontein kimberlite (Kimberley, South Africa). Sample BK consists of abundant macrocrysts (N1 mm) and (micro-) phenocrysts of olivine and lesser phlogopite, smaller grains of apatite, serpentinised monticellite, spinel, perovskite, phlogopite and ilmenite in a matrix of calcite, serpentine and dolomite. As in kimberlites worldwide, BK olivine grains consist of cores with variable Mg/Fe ratios, overgrown by rims that host inclusions of groundmass phases (spinel, perovskite, phlogopite) and have constant Mg/Fe, but variable Ni, Mn and Ca concentrations. Primary multiphase inclusions in the outer rims of olivine and in Fe-Ti-rich (‘MUM’) spinel are dominated by dolomite, calcite and alkali carbonates with lesser silicate and oxide minerals. Secondary inclusions in olivine host an assemblage of Na-K carbonates and chlorides. The primary inclusions are interpreted as crystallised alkali-Si-bearing Ca-Mg-rich carbonate melts, whereas secondary inclusions host Na-K-rich C-O-H-Cl fluids. In situ Sr-isotope analyses of groundmass calcite and perovskite reveal similar 87Sr/86Sr ratios to perovskite in the Bultfontein and the other Kimberley kimberlites, i.e. magmatic values. The ?18O composition of the BK bulk carbonate fraction is above the mantle range, whereas the ?13C values are similar to those of mantle-derived magmas. The occurrence of different generations of serpentine and occasional groundmass calcite with high 87Sr/86Sr, and elevated bulk carbonate ?18O values indicate that the kimberlite was overprinted by hydrothermal fluids, which probably included a significant groundwater component. Before this alteration the groundmass included calcite, monticellite, apatite and minor dolomite, phlogopite, spinel, perovskite and ilmenite. Inclusions of groundmass minerals in olivine rims and phlogopite phenocrysts show that olivine and phlogopite also belong to the magmatic assemblage. We therefore suggest that the crystallised kimberlite was produced by an alkali-bearing, phosphorus-rich, silica-dolomitic melt. The alkali-Si-bearing Ca-Mg-rich carbonate compositions of primary melt inclusions in the outer rims of olivine and in spinel grains with evolved compositions (MUM spinel) support formation of these melts after fractionation of abundant olivine, and probably other phases (e.g., ilmenite and chromite). Finally, the similarity between secondary inclusions in kimberlite olivine of this and other worldwide kimberlites and secondary inclusions in minerals of carbonatitic, mafic and felsic magmatic rocks, suggests trapping of residual Na-K-rich C-O-H-Cl fluids after groundmass crystallisation. These residual fluids may have persisted in pore spaces within the largely crystalline BK groundmass and subsequently mixed with larger volumes of external fluids, which triggered serpentine formation and localised carbonate recrystallisation.
The Archean sedimentary sulfur recycling under the Kaapvaal craton revisited from 4S- isotopic compositions in sulfide inclusions in diamonds from Kimberley Pool.
Canada, Northwest Territories, Quebec, United States, Colorado
deposit, A54, Lynx, Kelsey Lake
Abstract: Eighteen diamond samples from the A154 South kimberlite pipe (Diavik Mine), Slave Craton, Northwest Territories (Canada); sixteen diamond samples from the Lynx kimberlite dyke, Superior Craton, Quebec (Canada) and twelve diamond samples from the Kelsey Lake kimberlite pipe, Wyoming Craton, Colorado (USA), were cut through the core-zones, polished, imaged by cathodoluminescence (CL), and analyzed by secondary ion mass spectrometry (SIMS) for carbon isotope composition and nitrogen abundance. Twenty Kelsey Lake diamond plates, including the twelve crystals analyzed by SIMS, were analyzed by Fourier transform infrared spectrometry (FTIR) for nitrogen concentration and aggregation state. Diamond samples from Diavik and Kelsey Lake have average ?13CPDB and nitrogen contents (atomic ppm) similar to those found by earlier studies: averaging between ? 3.9‰ and 486 ppm, and ? 7‰ and 308 ppm, respectively. Samples from the Lynx dyke, investigated for the first time, are substantially different, having ?13C = ?1.2‰ and nitrogen content = 32 ppm (averages). All three localities have examples of significant variations in nitrogen content (> 100 ppm) within single stones. Carbon isotope variation within individual stones is relatively minor (< 2‰). In terms of nitrogen aggregation, samples from the Kelsey Lake kimberlite are dominated by zones of Type IaA, but mixed-type and Type IaB (less common) stones also occur. For the majority of samples, overall intra-diamond zonations of nitrogen abundances and carbon isotope ratios are not in agreement with modeled trends for single-event Rayleigh fractionation of diamond from fluid under nitrogen-compatible conditions at 1100 °C. The involvement of fluids from subducted crustal reservoirs with exceptionally light, and in the case of Lynx samples, exceptionally heavy ?13CPDB values is necessary to explain the observed growth histories of all the samples studied here.
Canada, Northwest Territories, Quebec, United States, Colorado
deposit, A54, Lynx, Kelsey Lake
Abstract: Eighteen diamond samples from the A154 South kimberlite pipe (Diavik Mine), Slave Craton, Northwest Territories (Canada); sixteen diamond samples from the Lynx kimberlite dyke, Superior Craton, Quebec (Canada) and twelve diamond samples from the Kelsey Lake kimberlite pipe, Wyoming Craton, Colorado (USA), were cut through the core-zones, polished, imaged by cathodoluminescence (CL), and analyzed by secondary ion mass spectrometry (SIMS) for carbon isotope composition and nitrogen abundance. Twenty Kelsey Lake diamond plates, including the twelve crystals analyzed by SIMS, were analyzed by Fourier transform infrared spectrometry (FTIR) for nitrogen concentration and aggregation state. Diamond samples from Diavik and Kelsey Lake have average ?13CPDB and nitrogen contents (atomic ppm) similar to those found by earlier studies: averaging between ? 3.9‰ and 486 ppm, and ? 7‰ and 308 ppm, respectively. Samples from the Lynx dyke, investigated for the first time, are substantially different, having ?13C = ?1.2‰ and nitrogen content = 32 ppm (averages). All three localities have examples of significant variations in nitrogen content (> 100 ppm) within single stones. Carbon isotope variation within individual stones is relatively minor (< 2‰). In terms of nitrogen aggregation, samples from the Kelsey Lake kimberlite are dominated by zones of Type IaA, but mixed-type and Type IaB (less common) stones also occur. For the majority of samples, overall intra-diamond zonations of nitrogen abundances and carbon isotope ratios are not in agreement with modeled trends for single-event Rayleigh fractionation of diamond from fluid under nitrogen-compatible conditions at 1100 °C. The involvement of fluids from subducted crustal reservoirs with exceptionally light, and in the case of Lynx samples, exceptionally heavy ?13CPDB values is necessary to explain the observed growth histories of all the samples studied here.
Canada, Northwest Territories, Quebec, United States, Colorado
deposit, A54, Lynx, Kelsey Lake
Abstract: Eighteen diamond samples from the A154 South kimberlite pipe (Diavik Mine), Slave Craton, Northwest Territories (Canada); sixteen diamond samples from the Lynx kimberlite dyke, Superior Craton, Quebec (Canada) and twelve diamond samples from the Kelsey Lake kimberlite pipe, Wyoming Craton, Colorado (USA), were cut through the core-zones, polished, imaged by cathodoluminescence (CL), and analyzed by secondary ion mass spectrometry (SIMS) for carbon isotope composition and nitrogen abundance. Twenty Kelsey Lake diamond plates, including the twelve crystals analyzed by SIMS, were analyzed by Fourier transform infrared spectrometry (FTIR) for nitrogen concentration and aggregation state. Diamond samples from Diavik and Kelsey Lake have average ?13CPDB and nitrogen contents (atomic ppm) similar to those found by earlier studies: averaging between ? 3.9‰ and 486 ppm, and ? 7‰ and 308 ppm, respectively. Samples from the Lynx dyke, investigated for the first time, are substantially different, having ?13C = ?1.2‰ and nitrogen content = 32 ppm (averages). All three localities have examples of significant variations in nitrogen content (> 100 ppm) within single stones. Carbon isotope variation within individual stones is relatively minor (< 2‰). In terms of nitrogen aggregation, samples from the Kelsey Lake kimberlite are dominated by zones of Type IaA, but mixed-type and Type IaB (less common) stones also occur. For the majority of samples, overall intra-diamond zonations of nitrogen abundances and carbon isotope ratios are not in agreement with modeled trends for single-event Rayleigh fractionation of diamond from fluid under nitrogen-compatible conditions at 1100 °C. The involvement of fluids from subducted crustal reservoirs with exceptionally light, and in the case of Lynx samples, exceptionally heavy ?13CPDB values is necessary to explain the observed growth histories of all the samples studied here.
Canada, Northwest Territories, Quebec, United States, Colorado
deposit, A54, Lynx, Kelsey Lake
Abstract: Eighteen diamond samples from the A154 South kimberlite pipe (Diavik Mine), Slave Craton, Northwest Territories (Canada); sixteen diamond samples from the Lynx kimberlite dyke, Superior Craton, Quebec (Canada) and twelve diamond samples from the Kelsey Lake kimberlite pipe, Wyoming Craton, Colorado (USA), were cut through the core-zones, polished, imaged by cathodoluminescence (CL), and analyzed by secondary ion mass spectrometry (SIMS) for carbon isotope composition and nitrogen abundance. Twenty Kelsey Lake diamond plates, including the twelve crystals analyzed by SIMS, were analyzed by Fourier transform infrared spectrometry (FTIR) for nitrogen concentration and aggregation state. Diamond samples from Diavik and Kelsey Lake have average ?13CPDB and nitrogen contents (atomic ppm) similar to those found by earlier studies: averaging between ? 3.9‰ and 486 ppm, and ? 7‰ and 308 ppm, respectively. Samples from the Lynx dyke, investigated for the first time, are substantially different, having ?13C = ?1.2‰ and nitrogen content = 32 ppm (averages). All three localities have examples of significant variations in nitrogen content (> 100 ppm) within single stones. Carbon isotope variation within individual stones is relatively minor (< 2‰). In terms of nitrogen aggregation, samples from the Kelsey Lake kimberlite are dominated by zones of Type IaA, but mixed-type and Type IaB (less common) stones also occur. For the majority of samples, overall intra-diamond zonations of nitrogen abundances and carbon isotope ratios are not in agreement with modeled trends for single-event Rayleigh fractionation of diamond from fluid under nitrogen-compatible conditions at 1100 °C. The involvement of fluids from subducted crustal reservoirs with exceptionally light, and in the case of Lynx samples, exceptionally heavy ?13CPDB values is necessary to explain the observed growth histories of all the samples studied here.
Abstract: Porphyritic olivine kimberlitic breccia, discovered in the Dörbed Banner of Inner Mongolia, Western China, is referred to as Longtou Shan Kimberlite in our study. This kimberlite occurs as a pipe in the Halahuogete Formation of Bayan Obo Group. Zircon U–Pb ages of Longtou Shan Kimberlite reveals a Mesoproterozoic age of ~1,552 Ma, constraining the deposition age of Halahuogete Formation to the Mesoproterozoic. Compared with Mesoproterozoic kimberlite of the ancient landmass, it can be inferred that the North China Craton is a member of the Ur ancient continent of the Columbia supercontinent. Furthermore, according to the tectonic background of the Bayan Obo Group, we raise this possibility that “Bayan Obo Aulacogen” should be renamed the “Bayan Obo Continental Rift.”
Continuity of kimberley-type pyroclastic kimberlite phases within Renard 2 over 1,000 m depth - insights to the geological and emplacement model, Superior craton, Canada.
Abstract: Clinopyroxenite mantle xenoliths from Obnazhënnaya kimberlite pipe, NE part of Siberian craton (Russia), preserve porphyroclastic clinopyroxene with no less than two generations of garnet and orthopyroxene lamellae, sometimes together with rutile. Their crystallographic relationships are consistent with an origin by solid-state exsolution. According to reintegrated major-element chemistry and datasets for natural systems the homogeneous high-Al clinopyroxenes were previously in equilibrium within a T range of ~1400– 1500 ºC at a minimum P of 2 GPa. Ca and Al variations in a clinopyroxene assume exsolution to take place during a cooling accompanied by a compression. According to Al contents the growth of orthopyroxene lamellae in the rocks is continued down to ~850 ºC and 2.7 GPa. The xenoliths matrix assemblage of Cpx+Grt±Opx marks strain-induced recrystallization where the exsolution features in recrystallized minerals are absent. Later re-equilibration of the mineral assemblage occurred at 790–810 ºC and 3.0–3.2 GPa in the cratonic mantle prior to the removal of rocks by kimberlite melts; the reactions were controlled by the diffusion of Ca and Al in a pyroxene structure. It was noted that Sr in clinopyroxenes (284–556 ppm) increases from core to rim together with V (149–226 ppm) and Ca, opposite to Al content higher in the center of Cpx porphyroclasts. A positive Eu anomaly is significant both in clinopyroxenes and garnets (Eu/Eu* = 1.5–1.8 and 1.3–2.0, respectively). Substitution of Al for Si in the pyroxene tetrahedral sites has allowed charging balance for the substitution of additional trivalent REE into the pyroxene M2 site [1]. The process has affected to the Sr2+, Sm3+ and V3+ contents and Eu2+/Eu3+ relations responsible for the presence of Eu anomaly in a pyroxene. The work was supported by the grant of the President of the Russian Federation MK-2231.2017.5. The study with LAT was funded by NSF grant EAR-1144337.
Geochimica et Cosmochimica Acta, Vol. 213, pp. 574-592.
Africa, Botswana
deposit - Orapa
Abstract: Major- and trace-element compositions of garnet and clinopyroxene, as well as 87Sr/86Sr in clinopyroxene and ?18O in garnet in eclogite and pyroxenite xenoliths from Orapa, at the western margin of the Zimbabwe craton (central Botswana), were investigated in order to trace their origin and evolution in the mantle lithosphere. Two groups of eclogites are distinguished with respect to 87Sr/86Sr: One with moderate ratios (0.7026-0.7046) and another with 87Sr/86Sr >0.7048 to 0.7091. In the former group, heavy ?18O attests to low-temperature alteration on the ocean floor, while 87Sr/86Sr correlates with indices of low-pressure igneous processes (Eu/Eu?, Mg#, Sr/Y). This suggests relatively undisturbed long-term ingrowth of 87Sr at near-igneous Rb/Sr after metamorphism, despite the exposed craton margin setting. The high-87Sr/86Sr group has mainly mantle-like ?18O and is suggested to have interacted with a small-volume melt derived from an aged phlogopite-rich metasome. The overlap of diamondiferous and graphite-bearing eclogites and pyroxenites over a pressure interval of ?3.2 to 4.9 GPa is interpreted as reflecting a mantle parcel beneath Orapa that has moved out of the diamond stability field, due to a change in geotherm and/or decompression. Diamondiferous eclogites record lower median 87Sr/86Sr (0.7039) than graphite-bearing samples (0.7064) and carbon-free samples (0.7051), suggesting that interaction with the - possibly oxidising - metasome-derived melt caused carbon removal in some eclogites, while catalysing the conversion of diamond to graphite in others. This highlights the role of small-volume melts in modulating the lithospheric carbon cycle. Compared to diamondiferous eclogites, eclogitic inclusions in diamonds are restricted to high FeO and low SiO2, CaO and Na2O contents, they record higher equilibrium temperatures and garnets have mostly mantle-like O isotopic composition. We suggest that this signature was imparted by a sublithospheric melt with contributions from a clinopyroxene-rich source, possibly related to the ca. 2.0 Ga Bushveld event.
Earth and Planetary Science Letters, Vol. 474, pp. 283-295.
Africa, South Africa
deposit - Lace
Abstract: Reconstructing the redox state of the mantle is critical in discussing the evolution of atmospheric composition through time. Kimberlite-borne mantle eclogite xenoliths, commonly interpreted as representing former oceanic crust, may record the chemical and physical state of Archaean and Proterozoic convecting mantle sources that generated their magmatic protoliths. However, their message is generally obscured by a range of primary (igneous differentiation) and secondary processes (seawater alteration, metamorphism, metasomatism). Here, we report the Fe3+/?Fe ratio and ?18 O in garnet from in a suite of well-characterised mantle eclogite and pyroxenite xenoliths hosted in the Lace kimberlite (Kaapvaal craton), which originated as ca. 3 Ga-old ocean floor. Fe3+/?Fe in garnet (0.01 to 0.063, median 0.02; n = 16) shows a negative correlation with jadeite content in clinopyroxene, suggesting increased partitioning of Fe3+ into clinopyroxene in the presence of monovalent cations with which it can form coupled substitutions. Jadeite-corrected Fe3+/?Fe in garnet shows a broad negative trend with Eu*, consistent with incompatible behaviour of Fe3+ during olivine-plagioclase accumulation in the protoliths. This trend is partially obscured by increasing Fe3+ partitioning into garnet along a conductive cratonic geotherm. In contrast, NMORB-normalised Nd/Yb - a proxy of partial melt loss from subducting oceanic crust (<1) and metasomatism by LREE-enriched liquids (>1) - shows no obvious correlation with Fe3+/?Fe, nor does garnet ?18OVSMOW (5.14 to 6.21‰) point to significant seawater alteration. Median bulk-rock Fe3+/?Fe is roughly estimated at 0.025. This observation agrees with V/Sc systematics, which collectively point to a reduced Archaean convecting mantle source to the igneous protoliths of these eclogites compared to the modern MORB source. Oxygen fugacites (fO2) relative to the fayalite-magnetite-quartz buffer (FMQ) range from ?log ? fO2 = FMQ-1.3 to FMQ-4.6. At those reducing conditions, the solubility of carbon in the fluids released by dehydration is higher than in fluids closer to FMQ. The implication is that Archean processes of C transport and deposition would have differed from those known in modern-style subduction zones, and diamond would have formed from methane-rich fluids. In addition, such reducing material could drive redox melting or freezing upon deep recycling and migration of CH4-bearing fluids into the ambient mantle.
Abstract: Stable calcium isotopic composition (44/40Ca) of silicate rock standards show limited variability [c.f., 1] although, fractionation between co-exiting ortho- and clino-pyroxenes have been reported [2]. Variability in 44/40Ca in Hawaiian shield stage tholeiites have been interpreted as evidence of subducted ancient marine carbonates, with very low 44/40Ca, into the Hawaiian plume [3]. Carbonatites are unique mantlederived carbonate-bearing igneous rocks with limited spatial but wide temporal occurrences. Few available measurements (n=5) of 44/40Ca in whole rock and leached carbonatites show a 0.2 ‰ range but broadly overlapping values with mantle-derived silicate rocks from different tectonic settings [1,4]. However, boron isotopic composition of global carbonatites suggest the contribution of subducted crustal component to the mantle source of relatively young carbonatites (<300 Ma old) [5], a signature which should potentially be traceable using Ca isotopes. We report 44/40Ca of global carbonatites ranging in age from Proterozoic to recent. The samples were analyzed using a 43Ca- 48Ca double spike on a Thermo Fischer Triton Plus Thermal Ionization Mass Spectrometer (TIMS) at IISc. 44/40Ca in the carbonatites (n = 11) range from 0.47 - 0.97 ‰ (w.r.t. SRM 915a). Our external reproducibility, estimated from multiple analyses of NIST standards SRM 915a, SRM 915b and seawater (NASS6), is better than 0.1 ‰ (2SD). 44/40Ca of the ~65 Ma old Ambadongar carbonatites of India, associated with eruption of the Deccan Traps, show correlations with Nb/Yb, K/Rb as well as with Sr/Nb, Sr/Zr. These variations suggest the role of phlogopite versus amphibole in the mantle source as well as subducted carbonates in controlling the 44/40Ca of these carbonatites.
Journal of Structural Geology, Vol. 86, pp. 47-61.
Africa, South Africa
deposit - Venetia
Abstract: The Beit Bridge Complex of the Central Zone (CZ) of the Limpopo Belt hosts the 519 ± 6 Ma Venetia kimberlite diatremes. Deformed shelf- or platform-type supracrustal sequences include the Mount Dowe, Malala Drift and Gumbu Groups, comprising quartzofeldspathic units, biotite-bearing gneiss, quartzite, metapelite, metacalcsilicate and ortho- and para-amphibolite. Previous studies define tectonometamorphic events at 3.3-3.1 Ga, 2.7-2.5 Ga and 2.04 Ga. Detailed structural mapping over 10 years highlights four deformation events at Venetia. Rules-based implicit 3D modelling in Leapfrog Geo™ provides an unprecedented insight into CZ ductile deformation and sheath folding. D1 juxtaposed gneisses against metasediments. D2 produced a pervasive axial planar foliation (S2) to isoclinal F2 folds. Sheared lithological contacts and S2 were refolded into regional, open, predominantly southward-verging, E-W trending F3 folds. Intrusion of a hornblendite protolith occurred at high angles to incipient S2. Constrictional-prolate D4 shows moderately NE-plunging azimuths defined by elongated hornblendite lenses, andalusite crystals in metapelite, crenulations in fuchsitic quartzite and sheath folding. D4 overlaps with a: 1) 2.03-2.01 Ga regional M3 metamorphic overprint; b) transpressional deformation at 2.2-1.9 Ga and c) 2.03 Ga transpressional, dextral shearing and thrusting around the CZ and d) formation of the Avoca, Bellavue and Baklykraal sheath folds and parallel lineations.
Abstract: The nitrogen isotopic composition of mantle samples lie between -15 to -5 ‰ and, is different from subducted sediments that varies between +6 to +15 ‰. As a result, N can be an excellent tracer of a subducted component [e.g. 1]. We have studied N from Indian carbonatites of adjacent locations in Hogenakal (2700 Ma) and Sevattur (770 Ma) with established mantle origin. We have also studied two diamonds representative of the Witwatersrand basin (2900–2700 Ma) and Jagersfontein (1100-1700 Ma) belonging to the Kapvaal supergroup. Both India and the Kapvaal craton formed part of a supercontinent that persisted as coherent units until the breakup of Pangea. Comparing the N in these diamonds with the carbonatites will put constraints on differences in their sources and the role of subduction in their generation. The nitrogen isotopic composition of the carbonatites are comparable ranging between -3 to +13 ‰, although value as low as -22 ‰ is observed from an apatite from Hogenakal. The N contents vary from 130 to 6000 ppb. Of the diamonds, Jagersfontein have ?15N of +2.3 and +9.3 ‰, while those from the Witwatersrand basin are –2.3 and 0 ‰. Their nitrogen lie between 500-900 ppm. These results have important implications for their formation and sources.
Abstract: The nitrogen isotopic composition of mantle samples lie between -15 to -5 ‰ and, is different from subducted sediments that varies between +6 to +15 ‰. As a result, N can be an excellent tracer of a subducted component [e.g. 1]. We have studied N from Indian carbonatites of adjacent locations in Hogenakal (2700 Ma) and Sevattur (770 Ma) with established mantle origin. We have also studied two diamonds representative of the Witwatersrand basin (2900–2700 Ma) and Jagersfontein (1100-1700 Ma) belonging to the Kapvaal supergroup. Both India and the Kapvaal craton formed part of a supercontinent that persisted as coherent units until the breakup of Pangea. Comparing the N in these diamonds with the carbonatites will put constraints on differences in their sources and the role of subduction in their generation. The nitrogen isotopic composition of the carbonatites are comparable ranging between -3 to +13 ‰, although value as low as -22 ‰ is observed from an apatite from Hogenakal. The N contents vary from 130 to 6000 ppb. Of the diamonds, Jagersfontein have ?15N of +2.3 and +9.3 ‰, while those from the Witwatersrand basin are –2.3 and 0 ‰. Their nitrogen lie between 500-900 ppm. These results have important implications for their formation and sources.
Abstract: Fluid inclusions trapped during diamond formation provide pristine information into the nature of mantle volatile sources. The majority of diamonds are formed at the base of the lithosphere, which due to its non-convective nature is able to retain geochemical heterogeneities introduced through interactions with the upper and lower mantle, crustal, and subduction related sources. In order to evaluate the origin of diamond forming fluids in the lithosphere, we present noble gas isotopic data from a suite of cubic, coated and cloudy diamond from the Nyurbinskaya Kimberlite, Siberia. Noble gas signatures extracted from fluid inclusions by crushing show two distinct volatile components present within the Siberian lithosphere. Cubic diamonds have average 3 He/4 He of 10 RA, whilst the 3 He/4 He of the coated and cloudy diamonds is the 6 RA. The Ne isotopic data is also different between the diamonds with 20Ne/22Ne in the cubic diamonds (10.7) consistently higher that the coated and cloudy diamonds, which are dominated by an atmospheric component. The 3 He/4 He in fluids trapped in the coated and cloudy diamonds are typical of samples from the lithospheric mantle. Fluids trapped in the cubic diamonds have higher 3 He/4 He than lithospheric and MORB mantle sources, but are similar to values reported from the Siberian Flood Basalts (SFB), which are derived from a lower mantle source. Ne isotopic data from the cubic diamond also suggests these diamonds contain a lower mantle volatile component. Noble gases in diamond hosted fluid inclusions have shown the Siberian lithosphere contains both lihtospheric and lower mantle volatile compponents. The coexistence of lithospheric and lower mantle volatiles within diamonds originating from the same kimberlite indicates the Siberian lithosphere must have had at least two periods of diamond growth from two distinct diamond forming fluids.
Abstract: Fluid inclusions trapped during diamond formation provide pristine information into the nature of mantle volatile sources. The majority of diamonds are formed at the base of the lithosphere, which due to its non-convective nature is able to retain geochemical heterogeneities introduced through interactions with the upper and lower mantle, crustal, and subduction related sources. In order to evaluate the origin of diamond forming fluids in the lithosphere, we present noble gas isotopic data from a suite of cubic, coated and cloudy diamond from the Nyurbinskaya Kimberlite, Siberia. Noble gas signatures extracted from fluid inclusions by crushing show two distinct volatile components present within the Siberian lithosphere. Cubic diamonds have average 3 He/4 He of 10 RA, whilst the 3 He/4 He of the coated and cloudy diamonds is the 6 RA. The Ne isotopic data is also different between the diamonds with 20Ne/22Ne in the cubic diamonds (10.7) consistently higher that the coated and cloudy diamonds, which are dominated by an atmospheric component. The 3 He/4 He in fluids trapped in the coated and cloudy diamonds are typical of samples from the lithospheric mantle. Fluids trapped in the cubic diamonds have higher 3 He/4 He than lithospheric and MORB mantle sources, but are similar to values reported from the Siberian Flood Basalts (SFB), which are derived from a lower mantle source. Ne isotopic data from the cubic diamond also suggests these diamonds contain a lower mantle volatile component. Noble gases in diamond hosted fluid inclusions have shown the Siberian lithosphere contains both lihtospheric and lower mantle volatile compponents. The coexistence of lithospheric and lower mantle volatiles within diamonds originating from the same kimberlite indicates the Siberian lithosphere must have had at least two periods of diamond growth from two distinct diamond forming fluids.
Abstract: Carbonate-fluorapatite (also known as staffelite and/or francolite) can become a rock-forming mineral in the upper levels of some carbonatite complexes, such as at Sokli, Finland, and Kovdor, Russia. Carbonate-fluorapatite rocks are recognised as an important phosphate resource, but there is little consensus on their genesis. Two principal models are favoured: (1) a hydrothermal origin, from a late-stage, carbonatite-derived fluid or, (2) formation through supergene dissolution of carbonate and re-precipitation of apatite. In this contribution, we have investigated the texture and composition of different carbonate-fluorapatite generations (using cathodoluminescence microsopy and LA ICP MS) in order to evaluate the aforementioned formation mechanisms. Four carbonate-fluorapatite growth generations were identified: (1) primary apatite grains, with a rounded/euhedral habit and luminescing purple; (2) strongly luminescent epitactic rims on primary grains; (3) ‘aggregate’ apatite, forming a fine-grained groundmass, typically luminescing blue; (4) botryoidal growth zones, commonly luminescing blue, but in places green or non-luminescent. REE contents in secondary carbonate-fluorapatite generations (2–4) are markedly low, with some analyses below detection limit (typically <1 ppm). Furthermore, many of these analyses exhibit both positive and negative Ce anomalies, indicative of an oxidising environment. The low REE contents of the different carbonatefluorapatite generations indicates that negligible REE transfer occurred between different growth events, contrasting with hydrothermal apatite in other carbonatite complexes. Furthermore, the lack of any significant fractionation between subsequent carbonate-fluorapatite generations is interpreted as circumstantial evidence that these rocks did not form through hydrothermal alteration. This is compounded by the presence of a Ce anomaly, which is commonly interpreted as a weathering feature. While hydrothermal formation under different conditions, causing complete removal of the REE, cannot be ruled out, we conclude that the locations were, most-likely, formed in a supergene environment. Continued investigation of weathered carbonate-fluorapatite material from other localities is underway to assess this conclusion.
Abstract: Carbonate-fluorapatite (also known as staffelite and/or francolite) can become a rock-forming mineral in the upper levels of some carbonatite complexes, such as at Sokli, Finland, and Kovdor, Russia. Carbonate-fluorapatite rocks are recognised as an important phosphate resource, but there is little consensus on their genesis. Two principal models are favoured: (1) a hydrothermal origin, from a late-stage, carbonatite-derived fluid or, (2) formation through supergene dissolution of carbonate and re-precipitation of apatite. In this contribution, we have investigated the texture and composition of different carbonate-fluorapatite generations (using cathodoluminescence microsopy and LA ICP MS) in order to evaluate the aforementioned formation mechanisms. Four carbonate-fluorapatite growth generations were identified: (1) primary apatite grains, with a rounded/euhedral habit and luminescing purple; (2) strongly luminescent epitactic rims on primary grains; (3) ‘aggregate’ apatite, forming a fine-grained groundmass, typically luminescing blue; (4) botryoidal growth zones, commonly luminescing blue, but in places green or non-luminescent. REE contents in secondary carbonate-fluorapatite generations (2–4) are markedly low, with some analyses below detection limit (typically <1 ppm). Furthermore, many of these analyses exhibit both positive and negative Ce anomalies, indicative of an oxidising environment. The low REE contents of the different carbonatefluorapatite generations indicates that negligible REE transfer occurred between different growth events, contrasting with hydrothermal apatite in other carbonatite complexes. Furthermore, the lack of any significant fractionation between subsequent carbonate-fluorapatite generations is interpreted as circumstantial evidence that these rocks did not form through hydrothermal alteration. This is compounded by the presence of a Ce anomaly, which is commonly interpreted as a weathering feature. While hydrothermal formation under different conditions, causing complete removal of the REE, cannot be ruled out, we conclude that the locations were, most-likely, formed in a supergene environment. Continued investigation of weathered carbonate-fluorapatite material from other localities is underway to assess this conclusion.
Abstract: Carbonatites are the primary source of LREE worldwide. Here we describe evidence from the Okorusu mine in NorthCentral Namibia, based on results from a suite of techniques including SEM-EDS and SEM-CL imaging, EPMA, LA-ICPMS on minerals and fluid inclusions, bulk rock chemistry and microthermometry. This provides indications of hydrothermal reworking in a carbonatite-related REE deposit. The Okorusu deposit is part of a ring complex consisting of syenites, nepheline syenites, and carbonatite with hydrothermal fluorite ore mineralisation formed principally by replacing carbonatite bodies. The primary carbonatites show a typical LREE enriched pattern. Primary REE mineralisation is contained in the magmatic phases apatite, pyrochlore and calcite. These phases have been partially broken down by hydrothermal activity. Most of the REE in the carbonatite samples now occur in secondary hydrothermal phases, mainly synchysite-(Ce). The REE occur also as synchysite-(Ce) in the hydrothermal fluorite but additionally they are incorporated into the fluorite structure resulting in cathodoluminescence zoning. Fluid inclusions are observed in both magmatic phases (apatite, calcite and clinopyroxene) and in hydrothermal phases (fluorite, calcite and quartz). The fluid inclusions associated with secondary REE mineralisation in fluorite consist of liquid-vapour inclusion with a constant liquid/bubble ratio and often a small daughter mineral. This suggests that the REE were transported by a relatively concentrated aqueous fluid. Fluid and melt inclusions hosted in the magmatic phases show a wider range in composition. The Okorusu carbonatite deposit shows primary and secondary features common to carbonatite deposits worldwide, and so the results reported here may be of wider significance.
Abstract: The results of a study using scanning electron microscopy and atomic force microscopy comprising the micromorphology of the ditrigonal and trigonal layers on surfaces near the edges of octahedral diamond crystals from the Udachnaya-Eastern kimberlite pipe in Yakutia are presented. The studied surface sculptures are elongated parallel to the direction ?111? and have similar morphological features, characterized by a wavy profile across the lamination, the absence of flat areas at the micro- and nanolevel. It is proposed that both sculpture types were formed as a result of dissolution under natural conditions. This suggestion is corroborated by the revelation of negative trigons on the octahedral facets of the studied diamonds.
Abstract: EPMA data are obtained from the P-5 kimberlite from the Wajrakarur field in the Eastern Dharwar craton of southern India (EDC). The studied sample consists of xenocrysts and xenoliths set in a variable grain size groundmass of olivine (with two textures: rounded-anhedral and subhedraleuhedral), phlogopite, perovskite, spinel, pyroxene, spinel and spinel containing Ti-garnet core. Ti-rich garnet associated with spinel is a rare occurrence in kimberlites. Two types of spinel have been identified (a) fine grained (<80 ?m) and compositionally non titaniferous, and (b) large macrocrysts (>100 ?m) having replacement cores having distinctly Ti-rich (TiO2 up to 28.51 wt %) compositions. Spinel is an abundant phase varying from <20 to >300 ?m in size, mostly subhedral to euhedral in shape. Pipe-5 has atolland necklace-textured spinels in addition to the euhedral groundmass spinels. Apart from individual grains in ground mass spinel there are also spinel intergrowths with perovskite (no apparent reaction texture observed), and sieve-like intergrowths. The composition of groundmass spinel is extensively used as petrogenetic indicator mineral (Roeder and Schulze 2008). Ti-garnets contain significant Ti (21.25-28.51wt.% TiO2), Ca (15.45-27.69 wt.% CaO), Fe (2.62-24.46 wt.% FeO) and low Cr (0.08-1.52 wt.% Cr2O3) and low Al (1.40-3.87 wt.% Al2O3). Ti- garnets and their paragenetic relationships to spinel are considered here as vital petrogenetic indicators of metasomatic fluids (Dongre et al., 2016; Cheng et al., 2014), and textural association with spinel shows that Ti-garnet formed when early crystallizing spinel interacted with residual melt during magma crystallization.
Abstract: EPMA data are obtained from the P-5 kimberlite from the Wajrakarur field in the Eastern Dharwar craton of southern India (EDC). The studied sample consists of xenocrysts and xenoliths set in a variable grain size groundmass of olivine (with two textures: rounded-anhedral and subhedraleuhedral), phlogopite, perovskite, spinel, pyroxene, spinel and spinel containing Ti-garnet core. Ti-rich garnet associated with spinel is a rare occurrence in kimberlites. Two types of spinel have been identified (a) fine grained (<80 ?m) and compositionally non titaniferous, and (b) large macrocrysts (>100 ?m) having replacement cores having distinctly Ti-rich (TiO2 up to 28.51 wt %) compositions. Spinel is an abundant phase varying from <20 to >300 ?m in size, mostly subhedral to euhedral in shape. Pipe-5 has atolland necklace-textured spinels in addition to the euhedral groundmass spinels. Apart from individual grains in ground mass spinel there are also spinel intergrowths with perovskite (no apparent reaction texture observed), and sieve-like intergrowths. The composition of groundmass spinel is extensively used as petrogenetic indicator mineral (Roeder and Schulze 2008). Ti-garnets contain significant Ti (21.25-28.51wt.% TiO2), Ca (15.45-27.69 wt.% CaO), Fe (2.62-24.46 wt.% FeO) and low Cr (0.08-1.52 wt.% Cr2O3) and low Al (1.40-3.87 wt.% Al2O3). Ti- garnets and their paragenetic relationships to spinel are considered here as vital petrogenetic indicators of metasomatic fluids (Dongre et al., 2016; Cheng et al., 2014), and textural association with spinel shows that Ti-garnet formed when early crystallizing spinel interacted with residual melt during magma crystallization.
Abstract: Ihouhaouene area in In Ouzzal terrane (Hoggar, South Algeria) is exceptional by numerous carbonatite complexes systematically associated to syenites. They constitute one of the oldest carbonatite emplaced at 2 Ga. Various types of carbonatites are distinguished by their successive placement and pegmatitic to brecciated appearance. The first-generation of carbonatites are always brecciated with elements of syenite and carbonate cement with calcite, apatite, alkali feldspar, wollastonite, clinopyroxene +/- sphene, allanite, quartz and garnet. Late carbonatite intrusions appear in small pegmatitic veins rich in apatite (3-50 mm). All carbonatites are calciocarbonatites (38-50 wt% CaO) with silica content ranging from 5 to 21 wt% SiO2. The high silica content is interpreted as assimilation of syenite material during emplacement. Carbonatites have high Rare Earth Element (REE) concentrations with high Ligh REE/Heavy REE fractionation (e.g. 1088 ppm La, La/Yb= 144-198) and variable concentrations in Th (26.5-197 ppm). The REE concentrations are mainly controlled by apatite phenocrysts (30-40 vol.%) with 4-9 wt% REE. In late pegmatitic carbonatite, REE-rich apatites are green-yellow phenocrysts with britholite exsolution (up to 40 vol.%, Ca4(REE)6 (SiO4,PO4)6 (OH,F,Cl)2). Britholites are hexagonal and occur as fine lamellar exsolutions (<10 um) in the same crystallographic axis (001) than apatites or as irregularshaped grains (10-200 um). All britholites contain 8-16 wt% La, 21-43 wt% Ce and 7-12 wt% Nd. The apatite-britholite exsolutions correspond to a substitution of the trivalent rareearth elements (REE3+) and Si4+ for Ca2+ and P5+. The REE substitution is accompanied by a change in volatile composition with F-rich apatite and Cl-rich britholite indicating that Si and Cl-rich hydrothermal fluids are present at the late stage of carbonatite evolution leading to REEenrichment and the crystallization of REE minerals.
Abstract: Carbonatites are rare magmas containing almost no silica; the corresponding crystallized rocks represent the main rare earth elements (REE) deposits in production. Oldoinyo Lengai (Tanzania) is the only active carbonatite volcano on Earth, and may be used as a natural laboratory to identify the parameters responsible for the genesis of the >500 reported fossil occurrences of carbonatite magmas. Nevertheless the carbonatites emitted at Oldoinyo Lengai are unique as alkalirich (natrocarbonatites), and their origin may not be representative of the fossil carbonatites (calcio-, ferro-, magnesio-carbonatites). Here we use three-phases melt inclusions trapped in clinopyroxenes and nephelines from cognate cumulates – that sample the active magma chamber of Oldoinyo Lengai – emitted during the 2007-08 sub-plinian explosive eruption to track the carbonatite presence within the plumbing system, and to eventually quantify its composition at depth. We show that although natrocarbonatites are emitted at Oldoinyo Lengai summit, more classical calciocarbonatites are present at magma chamber depth, consistent with rare natrocarbonatites being derived from more classical calciocarbonatites by further magma differentiation. Those unique cognate samples allows us to provide the first direct measurements of partition coefficients for major and trace elements of natural coexisting in equilibrium carbonatite and silicate melts. Partition coefficients suggests that natrocarbonatites derive from calciocarbonatites by fractionating Ca-rich, and Na-poor phases. The Oldoinyo Lengai can therefore be used as a perfect analogue of fossil igneous systems that are now exhumed, commonly lacking any relation with the initial geodynamic setting, and form REE mineral deposits.
Abstract: Carbonatites are rare magmas containing almost no silica; the corresponding crystallized rocks represent the main rare earth elements (REE) deposits in production. Oldoinyo Lengai (Tanzania) is the only active carbonatite volcano on Earth, and may be used as a natural laboratory to identify the parameters responsible for the genesis of the >500 reported fossil occurrences of carbonatite magmas. Nevertheless the carbonatites emitted at Oldoinyo Lengai are unique as alkalirich (natrocarbonatites), and their origin may not be representative of the fossil carbonatites (calcio-, ferro-, magnesio-carbonatites). Here we use three-phases melt inclusions trapped in clinopyroxenes and nephelines from cognate cumulates – that sample the active magma chamber of Oldoinyo Lengai – emitted during the 2007-08 sub-plinian explosive eruption to track the carbonatite presence within the plumbing system, and to eventually quantify its composition at depth. We show that although natrocarbonatites are emitted at Oldoinyo Lengai summit, more classical calciocarbonatites are present at magma chamber depth, consistent with rare natrocarbonatites being derived from more classical calciocarbonatites by further magma differentiation. Those unique cognate samples allows us to provide the first direct measurements of partition coefficients for major and trace elements of natural coexisting in equilibrium carbonatite and silicate melts. Partition coefficients suggests that natrocarbonatites derive from calciocarbonatites by fractionating Ca-rich, and Na-poor phases. The Oldoinyo Lengai can therefore be used as a perfect analogue of fossil igneous systems that are now exhumed, commonly lacking any relation with the initial geodynamic setting, and form REE mineral deposits.
Abstract: The Palabora Carbonatite Complex (PCC) in South Africa intruded at 2060 Ma into Archean basement. The tripartite pipe-like intrusion is represented by a northern and southern pyroxenite and the central Loolekop pipe. Carbonatites and phoscorites of the Loolekop pipe experienced at least 4 stages of mineralization, recrystallization and redistibution reflected by an (1) orthomagmatic, (2) late-magmatic, (3) sulphide and (4) post-magmatic phase (Giebel et al., 2017). These four stages exhibit considerable variability of REE mineralization and especially stages 2 and 4 show intense fluid-rock interaction textures. We present microtextural and compositional data on apatite and phlogopite along a 2 km depth profile through the Loolekop pipe and investigate how these data reflect fluidmineral interaction with depth during stage (2). A special focus lies on understanding the behaviour, sources and sinks of REE elements. While fluid-apatite interaction causes a dissolution of apatite coupled with a precipitation of monazite at apatite rims, the fluid-phlogopite interaction induces a chloritization of phlogopite and an occasional formation of britholite along strongly dissolved phlogopite rims. We suspect that REE are transported into the system by this late-magmatic fluid rather than being released by the dissolution of orthomagmatic REE-bearing minerals. Combining these observations with fluid inclusion textures and microthermometry, we will investigate the nature and composition of the involved fluids and will try to model REE mineralisation processes during late-magmatic fluidmineral ineraction
Abstract: The origin of intraplate carbonatitic to alkaline volcanism in Africa is controversial. A tectonic control, i.e., decompression melting associated with far-field stress, is suggested by correlation with lithospheric sutures, repeated magmatic cycles in the same areas over several million years, synchronicity across the plate, and lack of clear age progression patterns. Conversely, a dominant role for mantle convection is supported by the coincidence of Cenozoic volcanism with regions of lithospheric uplift, positive free-air gravity anomalies, and slow seismic velocities. To improve constraints on the genesis of African volcanism, here we report the first radiometric and isotopic results for the Catanda complex, which hosts the only extrusive carbonatites in Angola. Apatite (U-Th-Sm)/He and phlogopite 40Ar/39Ar ages of Catanda aillikite lavas indicate eruption at ca. 500–800 ka, more than 100 m.y. after emplacement of abundant kimberlites and carbonatites in this region. The lavas share similar high-? (HIMU)–like Sr-Nd-Pb-Hf isotope compositions with other young mantle-derived volcanics from Africa (e.g., Northern Kenya Rift; Cameroon Line). The position of the Catanda complex in the Lucapa corridor, a long-lived extensional structure, suggests a possible tectonic control for the volcanism. The complex is also located on the Bié Dome, a broad region of fast Pleistocene uplift attributed to mantle upwelling. Seismic tomography models indicate convection of deep hot material beneath regions of active volcanism in Africa, including a large area encompassing Angola and northern Namibia. This is strong evidence that intraplate late Cenozoic volcanism, including the Catanda complex, resulted from the interplay between mantle convection and preexisting lithospheric heterogeneities.
Abstract: Metasomatism by fluid or melt is commonly attributed as the cause of chemical and modal heterogeneity observed in peridotite xenoliths from the sub-continental lithospheric mantle. Documented manifestations are (1) perturbation of the oxygen fugacity (fO2), which may affect the stability of carbon-bearing phases, and (2) trace-element enrichment, typified by the shape of REEN patterns. Garnet, which contains Fe2+ and Fe3+ in measurable quantities, and exhibits prominent variation in REEN patterns between samples, may record the metasomatic history of the mantle. Here we report variations of fO2 and trace element concentrations for a suite of 22 garnet-bearing peridotite xenoliths from the Louwrensia kimberlite, south-central Namibia. The xenoliths span an estimated pressure range between 2.7 and 4.5 GPa. Fe3+/?Fe of garnet was determined by Fe K-edge XANES spectroscopy. Concomitant fO2 was calculated using the oxybarometer calibration of Miller et al. [1]. The trace element concentrations of all phases were determined by LA-ICP-MS. A global dataset comprising 454 garnet REEN patterns from 19 kimberlites has been compiled. The REEN pattern of each sample was fit to orthogonal polynomial functions that parameterise the abundance, slope, quadratic curvature, and cubic curvature [2]. Quadratic and cubic curvature correlate with abundance, albeit with considerable scatter. There is, however, an absence of correlation between REEN patterns and fO2, depth, or modal abundance. This is in contrast to correlations and trends observed for basaltic melts that clearly identify petrogenetic trends. The partitioning of REEs between garnet and co-existing phases in these samples highlights pronounced trace-element disequilibrium and hence question the validity of considering garnet REEN in isolation as a means of discerning metasomatic history
Abstract: Metasomatism by fluid or melt is commonly attributed as the cause of chemical and modal heterogeneity observed in peridotite xenoliths from the sub-continental lithospheric mantle. Documented manifestations are (1) perturbation of the oxygen fugacity (fO2), which may affect the stability of carbon-bearing phases, and (2) trace-element enrichment, typified by the shape of REEN patterns. Garnet, which contains Fe2+ and Fe3+ in measurable quantities, and exhibits prominent variation in REEN patterns between samples, may record the metasomatic history of the mantle. Here we report variations of fO2 and trace element concentrations for a suite of 22 garnet-bearing peridotite xenoliths from the Louwrensia kimberlite, south-central Namibia. The xenoliths span an estimated pressure range between 2.7 and 4.5 GPa. Fe3+/?Fe of garnet was determined by Fe K-edge XANES spectroscopy. Concomitant fO2 was calculated using the oxybarometer calibration of Miller et al. [1]. The trace element concentrations of all phases were determined by LA-ICP-MS. A global dataset comprising 454 garnet REEN patterns from 19 kimberlites has been compiled. The REEN pattern of each sample was fit to orthogonal polynomial functions that parameterise the abundance, slope, quadratic curvature, and cubic curvature [2]. Quadratic and cubic curvature correlate with abundance, albeit with considerable scatter. There is, however, an absence of correlation between REEN patterns and fO2, depth, or modal abundance. This is in contrast to correlations and trends observed for basaltic melts that clearly identify petrogenetic trends. The partitioning of REEs between garnet and co-existing phases in these samples highlights pronounced trace-element disequilibrium and hence question the validity of considering garnet REEN in isolation as a means of discerning metasomatic history
Abstract: We report PGE data in xenoliths of the deformed and granular peridotites. The deformed peridotites are the most deep-seated rocks and represent a narrow range of depth (180-220 km) while granular peridotites are located throughout the section of the lithospheric mantle. PGE distribution in the deformed peridotites [1] generally corresponds to that in our granular peridotites and xenoliths from Lesotho [2]. But in contrast with broad range of PGE concentrations in granular peridotites, the deformed peridotites show nearly flat pattern from Os to Pt, except of Pd (Fig.1). Granular peridotites show good positive correlation between PGE and Fe2O3. We suppose that they enriched in PGE by iron phase during its evolution. As for deformed peridotites we propose that they were depleted in Ir and Os followed by the increase of Ga and Cpx on the first stage of mantle metasomatism. On the last stage the enrichment of Pt, Pd and Re was probably a result of submicron sulphide phase’s presipitation in the interstices of mantle rocks.
Abstract: The nitrogen concentration and aggregation form reflect the conditions of diamond formation and diamond evolution in primary source [1]. FTIR measurements were made on 40 colorless or slightly greenish octahedral diamonds from Snap Lake kimberlite dyke system. Studied diamonds differ in nitrogen content, distribution and aggregation degree. The total nitrogen content in different diamond zones is up to 1600 ppm. Diamonds have been classified into two groups on the basis of nitrogen aggregation degree in them. Group 1 includes poorly-aggregated-nitrogen diamonds. We suggest that such diamonds belong to the same generation such as cubic diamonds from Snap Lake [2]. The low degree of nitrogen aggregation in diamonds is indicative of short mantle residence and suggests that they crystallized shortly before kimberlite eruption. Diamonds of Group 2 are characterized by high nitrogen aggregation degree (up to 98.6%). Group 2 includes diamonds either with uniform nitrogen distribution throughout the crystal volume or with a predominance of Bdefect in the center. Inhomogeneity in nitrogen distribution from the center to the edge of the octahedral crystals indicates, at least, about the two, or even more growth stages of a part of the studied diamonds. High nitrogen aggregation degree according to “annealing” model is evidence of diamond staying in the high temperature region or of their residence in the mantle conditions. Results obtained support that significant part of octahedral diamonds from Snap Lake may have formed at the base of a thick lithospheric mantle at depth below 300 km [3].
Abstract: Metasomatised regions of Earth’s sub-continental lithospheric mantle potentially represent a large volatile reservoir. Nevertheless, the mechanisms involved in the storage and upward transport of volatiles such as C and S, from the convecting mantle and/or subducting slabs, are poorly understood. We have carried out a systematic microanalytical study of a suite of sulfide-rich mantle peridotites from the Bultfontein diamond mine, Kimberley. EDS mapping of large (>2mm), interstitial base metal sulfides in the Bultfontein xenoliths has identified distinct Ni-rich regions (pentlandite). The Ni-rich sulfides are adjacent to olivine with Ni poor rims (<0.2 wt% NiO). Diffusion profiles between the protolith olivines and adjacent sulfides are used to estimate the timing of the S-rich metasomatic event. The presence of large unequilibrated olivine indicates that Nisulfides were introduced immediately prior to kimberlite emplacement. The calculated composition of melt in equilibrium with metasomatic clinopyroxenes in the Bultfontein sulphide-bearing peridotites shows a strong correlation to high-density carbonatitic fluids trapped in diamonds. This association is extended by the wealth of metasomatic sulfides in the Bultfontein xenoliths. Moreover, Ni-rich sulfides (~25 wt%) are the most common mineral inclusion in peridotitic diamonds, implying that diamonds crystallise from a S-saturated fluid. Many studies attribute the metasomatism at Bultfontein to silicate melts associated with the kimberlite, but we explore the possibility of metasomatism by reactive percolation of a volatile-rich agent with carbonatitic affinity. The S-rich nature of the metasomatism and the correlation with diamond high-density fluids has great implications for the transport of volatiles from the deep mantle to shallow regions of the craton.
Abstract: Polycrystalline diamond aggregates (diamondites) are produced by rapid crystal nucleation caused by extreme carbon supersaturation in mantle fluids. They may form episodically and under variable chemical conditions, providing snapshots of diamond formation in the Earth’s mantle. Diamondites, thus, represent an extreme end member of diamond formation mechanisms, while forming via the same processes and ingredients as the gem-sized diamonds. We present results on a large suite of diamondites from the Venetia mine (South Africa), comprising a complete characterisation of the diamonds and their silicate inclusions and intergrowths. The highlighted characteristic of this sample suite is its heterogeneity in all aspects, from affiliated silicate to diamond composition and texture of the diamond aggregates. The diamond grains in the samples are intergrown with silicates (garnets, clinopyroxenes, phlogopites) comprising a websteritic-eclogitic and a peridotiticpyroxenitic suite of minerals. Diamonds, regardless of their affiliation based on their silicate phases, overlap in carbon and nitrogen composition and have ?13C values between -28 and -8 ‰, ?15N values of 0.8 to 16.3 ‰ and nitrogen contents of 4 to 2329 ppm. The entire range of carbon and nitrogen variability of the suite is also reflected in some individual samples. Cathodoluminescence imaging visualizes different zones in the samples that can be interpreted as different growth events with differing nitrogen contents and ?15N decoupled from ?13C values, in line with the variability off nitrogen aggregation states. Electron backscatter diffraction analyses identify an original texture of randomly intergrown diamond grains that is partly changed by deformation and newly grown smaller diamond grains. The large overall variability suggesting episodic formation of diamondite with nitrogen from crustal sources.
South African Institute of Mining and Metallurgy, Vol. 116, 8, pp. 731-737.
Africa, Namibia
deposit - Orange River
Abstract: Over the past 80 years, the Namibian diamondiferous marine placer has been studied extensively to develop solutions for mining and sampling challenges. The types of studies include the statistical modelling of the distributions of the stone counts per sample; investigating the relationship between geology and the grade distribution; assessing the quality potential of the entrapment of the available diamond pulse; using predetermined acceptability of barren samples (zero proportion (Zp) samples) to model distributions; optimal sample sizes; and more. During early-stage project evaluation it is more important to find out if a particular area is likely to be above a specific cut-off grade than to focus on sampling for the purpose of accurate resource estimation. Previous work using mixed Poisson and Sichel distributions to model the abundant onshore diamond data has been very successful in modelling the long-tailed nature of these linear beach deposits. The means of these distributions are, however, sensitive to extreme values. Technical and cost constraints prevent a similar scale of sample collection in an adjacent, geologically equivalent, submerged beach environment. A method not sensitive to extreme values is thus required to make early-stage assessments of the likelihood that the grade of a particular target is above a minimum cut-off grade. The Nachman model describes the functional relationship between the mean population density and proportion of barren patches ( Zp) in a patchy environment. A prerequisite for using the Nachman model is that the underlying data must be modelled using a negative binomial distribution (NBD). The case study data is from an analogous area adjacent to the exploration target and meets the NBD requirement. It is thus appropriate to apply the Nachman model. The Nachman model provides an opportunity to use the observed Zpto predict the mean grade for an area at the very early stage of an exploration project. In future, early-stage exploration data from a homogenous geological zone exhibiting characteristics of the Nachman model assumptions can thus be used to rank and target those areas that show potential to be above the minimum required grade cut-off for follow-up sampling and inclusion in the mine planning cycle.
South African Institute of Mining and Metallurgy, Vol. 116, 8, pp. 745-752.
Africa, South Africa
deposit - Cullinan
Abstract: In 2012, Cullinan Diamond Mine began an expansion programme with the shaft deepening and development of access to the C-Cut 1 block at approximately 839 m below surface. The expansion programme is funded by a combination of bank loans and retained operating profit generated by the mine. Continuous production during deepening of the No. 1 Shaft, which is the rock hoisting shaft, was therefore critical for sustainability and efficiency as well as overall funding of the project. The deepening method, support design and verification, as well as learning outcomes pertaining to the extension of the No. 1 Shaft underneath the existing operating shaft are summarized, with emphasis on the importance of gaining some understanding of the shaft's host rock mass.
Abstract: The modal metasomatic alteration for lithosphere mantle may be investigated using mantle xenoliths from kimberlite pipes. The mantle xenoliths from upper-Jurassic Obnajennaya kimberlite pipe (Kuoika field, Yakutia) were studied. Three main xenoliths groups in Obnajennaya pipe were distinguished based on the petrographic and geochemical features: 1. Sp, Sp-Grt, Grt harzburgites - lherzolites, Sp, Sp-Grt, Grt olivine websterites and Sp, Sp-Grt, Grt websterite (so-called magnesium group - about 80 % from xenoliths). The high magnesium mineral composition, high estimated temperature (1250 - 1500°?) for exsolution pyroxene megacrystals, presence of sulphide globules and distribution curves for rare earth elements in garnets (La-Yb increasing) are to assume the crystallisation from melt. The 10% magnesium mantle xenoliths are observed the secondary metasomatic phlogopite and amphibole (pargasite). The clinopyroxene distribution curves demonstrate the wide range of values and altered samples show higher content HFSE group elements that primary clinopyroxene. The increasing of HFSE and rare earth element concentrations can also be traced by the amphibole chemical composition. The 40Ar/39Ar dating of phlogopite from was result 1639 ± 5 Ma nearly corresponding to the time of Siberian craton accretion Thus during Siberian craton accretion (about 1.7 Ga) the melts-fluids enriching Nb + Ta and REE impacted on lithosphere mantle under Kuoika field. 2. Eclogites and Grt clinopyroxenites with similar mineral composition (about 10-15% xenoliths). The high ?O18 for garnet and clinopyroxene (5.7–5.8‰) allows to assume subduction genesis. 3. Phl-Ilm rocks characterizing ferrous mineral composition (~ 10 % xenoliths). This group are charactetrized are ferrous mineral composition. The 40Ar/39Ar phlogopite dating resulted to 800-500 Ma, signed the potassium and titanium metasomatic fluide – melt influenced
Abstract: The use of confocal HR-Raman mapping opens new perspectives in studying melt inclusions. Our major goal is to show advantages of this powerful technique through case studies carried out on alkaline and carbonatite rocks of Kerimasi volcano (East African Rift). Raman spectrometry is one of the few methods that enable qualitative nondestructive analysis of both solid and fluid phases, therefore it is widely used for the identification of minerals and volatiles within melt and fluid inclusions. For better understanding of petrogenetic processes in carbonatite systems it is essential to find all mineral phases in the melt inclusions trapped in intrusive or volcanic rocks. Previous Raman spectroscopic point measurements in melt inclusions revealed the presence of daughter phases (e.g. alkali carbonates, hydrocarbonates) [1] but utilizing Raman mapping on them even provides information on their size, shape and distribution. Raman 3D mapping were applied on unheated multiphase melt inclusions of intrusive and volcanic rocks with high spatial resolution (XY plane < 1 micron) with a depth scan (Z step) as low as 0.5 micron at every XY point, parallel to the surface of the host minerals. Analysis below the surface of the host mineral is especially useful because we can avoid the loss of sensitive (e.g. water soluble) phases and contamination of the melt inclusions, moreover unexposed melt inclusions are suitable for further analytical measurements (e.g. EPMA, microthermometry). By scanning multiple layers 2D or 3D Raman images can be gained, thus we can get an insight into post entrapment crystallization processes that contribute to a more precise description of the evolution of alkaline and carbonatite rocks.
Abstract: Here we present major (EMPA) and trace element (SIMS, LA-ICP-MS) data for garnet and clinopyroxene from mantlederived xenoliths of coarse and sheared garnet peridotite [1, 2] and clinopyroxene-phlogopite metasomatic rocks from the Grib kimberlite, the Arkhangelsk diamond province, Russia, and provide new insights into the metasomatic processes that occur within the subcontinental lithospheric mantle (SCLM) during the kimberlite melts generation and ascent. The obtained data allowed us to reconstruct the following sequence of metasomatic events associated with the generation of the Grib kimberlite: 1. Ascent of high-temperature asthenospheric or mantle plume material resulted in a partial melting of a carbonated peridotite and led to the generation of high-temperature REEenriched proto-kimberlite melts containing significant amounts of carbonate, Fe-Ti and K-H2O. These protokimberlite melts started to interact with the surrounding mantle rocks during its evolution and ascent, and caused metasomatic modification of both coarse and sheared peridotites at the base of SCLM (T and P estimates are 1220°C and 70 kbar). 2. Further evolution of proto-kimberlite melts during the ascent and the interaction with the surrounding mantle (e.g. mantle-rock assimilation and/or percolative fractional crystallization) led to changes in the kimberlite composition from REE-enriched carbonate-dominated to carbonate-rich ultramafic silicate magmas with lower REE contents. 3. During the ascent, carbonate-rich ultramafic silicate kimberlite melts progressively metasomatised sorrounding SCLM from garnet-phlogopite peridotite through garnetphlogopite peridotite to clinopyroxene-phlogopite rocks under T and P estimated as 830°C and 40 kbar. At this stage, the fractionated of Fe-Ti-bearing megacrysts occurred.
Abstract: Diamond inclusions are the only samples from the mantle transition zone (410-660 km) and the lower mantle. Majoritic garnet is a rare inclusion, limited to pressures of ~8-20 Gpa with Si content being indicative of depth of re-equilibration. These garnet inclusions can therefore provide information on properties of the transition zone such as oxidation state. In this study, we used Synchrotron Mössbauer Source (SMS) to determine the ferric-ferrous ratios of 13 small (30 to 100 micrometers diameter) majoritic inclusions in diamonds from Jagersfontein. The studied inclusions have pyroxenitic affinities [1], with compositions intermediate between typical peridotite and eclogite. They contain 4.62-11.2 wt% CaO, 0.03-0.34 wt% Cr2O3 and Mg# of 0.65-0.81. Minimum pressures for their equilibration using Beyer and Frost [2] barometer are between 8 and 18 GPa with at least 4 of these inclusions being formed in the transition zone. The Fe3+/Fetotal ratios in the garnets increase from 0.08±0.01 to 0.30±0.03 with increasing pressure. These values define a clear extension of the trend apparent in the data from peridotite xenoliths crystallised at lower pressures. Thermodynamic calculations suggest that these high ferric contents correspond to oxygen fugacities above the FeFeO (IW) buffer, which means that the high Fe3+ contents were not generated by disproportionation of Fe2+ to Fe3+ and Fe0 . It is more likely that carbonate was the oxidising agent responsible for generating the high Fe3+ of these garnets.
Abstract: Diamond inclusions are the only samples from the mantle transition zone (410-660 km) and the lower mantle. Majoritic garnet is a rare inclusion, limited to pressures of ~8-20 Gpa with Si content being indicative of depth of re-equilibration. These garnet inclusions can therefore provide information on properties of the transition zone such as oxidation state. In this study, we used Synchrotron Mössbauer Source (SMS) to determine the ferric-ferrous ratios of 13 small (30 to 100 micrometers diameter) majoritic inclusions in diamonds from Jagersfontein. The studied inclusions have pyroxenitic affinities [1], with compositions intermediate between typical peridotite and eclogite. They contain 4.62-11.2 wt% CaO, 0.03-0.34 wt% Cr2O3 and Mg# of 0.65-0.81. Minimum pressures for their equilibration using Beyer and Frost [2] barometer are between 8 and 18 GPa with at least 4 of these inclusions being formed in the transition zone. The Fe3+/Fetotal ratios in the garnets increase from 0.08±0.01 to 0.30±0.03 with increasing pressure. These values define a clear extension of the trend apparent in the data from peridotite xenoliths crystallised at lower pressures. Thermodynamic calculations suggest that these high ferric contents correspond to oxygen fugacities above the FeFeO (IW) buffer, which means that the high Fe3+ contents were not generated by disproportionation of Fe2+ to Fe3+ and Fe0 . It is more likely that carbonate was the oxidising agent responsible for generating the high Fe3+ of these garnets.
Abstract: Salty fluids are stable in the lithospheric mantle [1] and thus we may expect to find them in extrusive volcanic rocks as well. In Siberia, the Udachnaya-East kimberlite hosts extremely well preserved ‘nodules’ of molten salts that do not present any relicts sedimentary textures [2]. It is still debated, however, whether these nodules are genetically linked to the kimberlitic magma. Here we used a combination of radiogenic (Rb-Sr, SmNd) and stable (S) isotopes analyses to investigate the origin of these nodules Salt-rich nodules, including chloride (95% chloride; n=2) and chloride-carbonate nodules (70% chloride + 30% alkali-carbonate; n=2) were studied, as well as host kimberlites (n=4), country-rock sediment and regional brine for comparison. On an evolution diagram, water and acetic acid leachates of chloride nodules define a linear array that, if interpreted as an isochron, yields an apparent age of 355 Ma, within error of the emplacement age of the kimberlite and an initial 87Sr/86Srt=355Ma of 0.710 ± 0.003. Bulk and carbonate fractions of chloride-carbonate nodules define an initial 87Sr/86Srt=355Ma (0.706 ±0.002) and 143Nd/144Ndt=355Ma (0.5123 ±0.0002) that overlap with those of the kimberlite (initial 87Sr/86Srt=355Ma =0.705 ±0.001 and 143Nd/144Ndt=355Ma =0.5124 ±0.0001). 87Sr/86Srt=355Ma of the brine and host sediment (0.7088) cannot explain the Sr isotopic composition of the chloride nodules. A dual origin for the nodules is thus possible, depending on their carbonate contents. In terms of sulfur isotopes, sulfates of the chloridecarbonate nodules and the salty kimberlite are undistinguishable (?34S=11‰). Sulfates of a chloride nodule have distinctly heavier isotopic compositions (?34S=18‰) but their Sr isotopes imply they cannot be explained by the assimilation of known sedimentary components or post magmatic fluid circulation (?34S=34‰ for host sediment and brine). In this contribution, we will discuss the robustness of both approches and propose some explanation(s) for the occurence of these salt nodules.
Abstract: Salty fluids are stable in the lithospheric mantle [1] and thus we may expect to find them in extrusive volcanic rocks as well. In Siberia, the Udachnaya-East kimberlite hosts extremely well preserved ‘nodules’ of molten salts that do not present any relicts sedimentary textures [2]. It is still debated, however, whether these nodules are genetically linked to the kimberlitic magma. Here we used a combination of radiogenic (Rb-Sr, SmNd) and stable (S) isotopes analyses to investigate the origin of these nodules Salt-rich nodules, including chloride (95% chloride; n=2) and chloride-carbonate nodules (70% chloride + 30% alkali-carbonate; n=2) were studied, as well as host kimberlites (n=4), country-rock sediment and regional brine for comparison. On an evolution diagram, water and acetic acid leachates of chloride nodules define a linear array that, if interpreted as an isochron, yields an apparent age of 355 Ma, within error of the emplacement age of the kimberlite and an initial 87Sr/86Srt=355Ma of 0.710 ± 0.003. Bulk and carbonate fractions of chloride-carbonate nodules define an initial 87Sr/86Srt=355Ma (0.706 ±0.002) and 143Nd/144Ndt=355Ma (0.5123 ±0.0002) that overlap with those of the kimberlite (initial 87Sr/86Srt=355Ma =0.705 ±0.001 and 143Nd/144Ndt=355Ma =0.5124 ±0.0001). 87Sr/86Srt=355Ma of the brine and host sediment (0.7088) cannot explain the Sr isotopic composition of the chloride nodules. A dual origin for the nodules is thus possible, depending on their carbonate contents. In terms of sulfur isotopes, sulfates of the chloridecarbonate nodules and the salty kimberlite are undistinguishable (?34S=11‰). Sulfates of a chloride nodule have distinctly heavier isotopic compositions (?34S=18‰) but their Sr isotopes imply they cannot be explained by the assimilation of known sedimentary components or post magmatic fluid circulation (?34S=34‰ for host sediment and brine). In this contribution, we will discuss the robustness of both approches and propose some explanation(s) for the occurence of these salt nodules.
Abstract: Is there the existence of a water-rich zone in the mantle, currently one of the most discussed problem in mantle petrology? There are recent studies of low-water content in nominally anhydrous minerals in diamonds [1] and the chemistry of exceptionally rare phlogopite inclusions coexisting with peridotitic and eclogitic minerals in kimberlite-hosted diamonds [2]. Previous studies have shown that some rapidly formed diamonds reflect the composition of the environment in which they formed [3]. The minerals trapped during nucleation stage remain shielded from any changing conditions during further diamond growth or later mantle metasomatism. Thus, the analysis of diamond microinclusions is a major tool for the direct study of mantle high-density fluids (HDFs) from which the diamonds have precipitated [4]. Using transmission electron microscopy (TEM) techniques, we have investigated hydrous silicates inside nanometerscale, polyphased unclusions, especially in dark cloudy alluvial and kimberlite diamonds. Clinohumite, phlogopite, and phengite were detected. Hydrous silicate phases are accompanied by Ba-Sr-Ca -Fe-Mg carbonates, in addition to sulfides, oxides (magnetite, rutile, ilmenite), F-apatite, KCl, graphite, and fluid bubbles. A contrast occurs between clinohumite associated with phlogopite, F-apatite and highMg carbonates, but phengite, accompanied by a Al, Kbearing, unidentified silicate. These inclusions reflect the composition of fluid from which the host diamond crystallized. The mica composition, in most cases, has excess Si, similar to the high-silica mica identified within diamond microinclusions from Diavik [5]. The fluid-bearing carbonatitic-silicic diamonds grew in water-rich environments with extremely high K-activity, compared to most diamonds, which grew only within limited zones in the Earth’s mantle.
South African Institute of Mining and Metallurgy, Vol. 116, 8, pp. 723-731.
Africa, Lesotho
deposit - Letseng
Abstract: The steepening of slope angles on an open pit mining operation has a material impact on improving the economics of mining. Steepening of slope angles can also increase the risk of slope failure. Slope failures are inherently costly events, because they can be catastrophic, resulting in multiple fatalities, equipment damage, and temporary or permanent closure of a mine. The steepening of the basalt slope angles at Letseng Diamond Mine followed operational improvements that were introduced through improved blasting practices and geotechnical controls. The steeper slope design resulted in a 6 Mt/a reduction in the peak waste mining compared with the previous mine plan coupled with an increase in the net present value and life of mine. This paper is an outline of the steps that were taken at Letseng to increase slope angles in waste and the resulting improvements to the mine plan.
Abstract: We report preliminary data for sulfur isotopes from two spatially related Neoproterozoic carbonatite complexes in Tamil Nadu, S India, with the aim of getting further insights into their magmatic and/or post-emplacement histories [1]. The major sulfide phase in these rocks is pyrite, with minor chalcopyrite, whereas sulfate occurs as barite. A bimodal distribution of G34Ssulfide is found for Samalpatti (13.5 to 14.0‰), and Sevattur (?2.1 to 1.4‰) carbonatites. A significantly larger range of G34Ssulfide values is found for the associated Samalpatti silicate rocks (?5.2 to 7.4‰) relative to Sevattur pyroxenites and gabbros (?1.1 to 2.1‰). High G34Ssulfide values for Samalpatti carbonatites are unsual [2,3] but could reflect hydrothermal post-emplacement modification [1] of S isotopes. The low G34Ssulfide values for Sevattur may represent a mantle source signature. The G34Ssulfate is uniformly positive for both complexes, with most data falling in a narrow range (5.7 to 7.8‰) and one datum for a pyroxenite yielding more positive G34Ssulfate = 13.3‰. Data for '33S varies outside of analytical uncertainty (?0.07 to 0.04‰), indicating contribution from a source with a surface-derrived component. The small range of '33S values does not allow us to determine whether these sources contain S fractionated by biogeochemical (mass-dependent) or photochemical (mass-independent, pre GOE) processes. Data for '36S is positive, and varies within uncertainty (0.28 ± 0.15‰). Variations of this magnitude have been observed in other localities, and are not diagnostic of any unique source or process. The sulfur isotope data imply addition of crustal sulfur to Samalpatti. In contrast, sulfur from Sevattur has a mantle-like G34S but '33S with anomalous character. These observations support the idea of a different evolutionary story for these complexes, possibly more complex than previously thought.
South African Institute of Mining and Metallurgy, Vol. 116, 4, pp. 343-350.
Africa, South Africa
deposit - Cullinan
Abstract: Near-infrared (NIR) spectroscopy sorting technology is incorporated in an automated optical mineral sorter that can discriminate between materials using the differences in characteristics when exposed to near-infrared radiation. During September 2014 to April 2015, a pilot plant that utilized NIR technology to discriminate between kimberlite and waste materials was commissioned to determine the viability of including this technology in the diamond winning process flow sheet at Cullinan Diamond Mine. The plant was used to minimize the waste content in the size fraction -70+35 mm that reports to the crushing section and then to the dense media separation process. This paper describes the initial test work, conducted at Mintek, that led to the decision to conduct a pilot-scale study. The mineralogical characterization of the feed and product streams to establish the sorting criteria and the operational data obtained during the pilot plant campaign are described. The results indicated a good possibility of discriminating between the kimberlite and waste material using NIR technology. However, the consistency of discrimination was not good enough to avoid the risk of potential diamond loss. Furthermore, a lower than expected availability of the machine reduced the throughput capabilities.
Geochimica et Cosmochimica Acta, in press available, 14p.
Europe, Finland
deposit - Kaavi
Abstract: We present high-precision isotope dilution data for Os, Ir, Ru, Pt, Pd and Re in Group I and Group II kimberlites from the Karelian craton, as well as 2 samples of the Premier Group I kimberlite pipe from the Kaapvaal craton. The samples have, on average, 1.38 ppb Pt and 1.33 ppb Pd, with Pt/Pd around unity. These PGE levels are markedly lower, by as much as 80%, than those reported previously for kimberlites from South Africa, Brazil and India, but overlap with PGE results reported recently from Canadian kimberlites. Primitive-mantle-normalised chalcophile element patterns are relatively flat from Os to Pt, but Cu, Ni and, somewhat less so, Au are enriched relative to the PGE (e.g., Cu/Pd > 25.000). Pd/Ir ratios are 3,6 on average, lower than in most other mantle melts. The PGE systematics can be largely explained by two components, (i) harzburgite/lherzolite detritus of the SCLM with relatively high IPGE (Os-Ir-Ru)/PPGE (Rh-Pt-Pd) ratios, and (ii) a melt component that has high PPGE/IPGE ratios. By using the concentrations of iridium in the kimberlites as a proxy for the proportion of mantle detritus in the magma, we estimate that the analysed kimberlites contain 3–27% entrained and partially dissolved detritus from the sub-continental lithospheric mantle, consistent with previous estimates of kimberlites elsewhere (Tappe S. et al., 2016, Chem. Geol. http://dx.doi.org/10.1016/j.chemgeo.2016.08.019). The other major component in the samples is melt, modelled to contain an average of 0.85 ppb Pt and 1.09 ppb Pd. Assuming that Group II kimberlites are derived from relatively metasomatised SCLM, our data suggest that the metasomatised Karelian SCLM is relatively poor in Pt and Pd. If our data are representative of other Group II kimberlites elsewhere, this result could imply that the PGE enrichment in certain continental large igneous provinces, including Bushveld, is not derived from melting of metasomatised SCLM.
Mollex, G., France, L., Furi, E., Bonnet, R., Botcharnikov, R.E., Zimmermann, L., Wilke, S., Deloule, E., Chazot, G., Kazimoto. E.O., Marty, B., Burnard, P.
Abstract: Cognate xenoliths that have been emitted during the last sub-plinian eruption in 2007-08 at Oldoinyo Lengai (OL) represent a unique opportunity to document the igneous processes occuring within the active magma chamber. Detailed petrographic descriptions coupled to a thermobarometric approach, and to the determination of volatile solubility models, allow us to identify the melt evolution at magma chamber conditions, and the storage parameters (P, T). Results indicate that a fresh phonolite melt (~1060°C) was injected into a crustal magma chamber at 11.5 ±3.5 km depth, in agreement with geophysical surveys performed during the eruption. The phonolite contains high volatile contents: 3.2 wt.% H2O and 1.4 wt.% CO2. The liquid line of descent highlights an evolution to nephelinite compositions by cooling down to 880°C. Our results support previous results related to this eruption, and are similar to the historical products emitted during the whole volcano history, allowing us to suggest that no major modification in the plumbing system has occured during the OL evolution. New noble gas results show that: i. fumaroles display constant He isotopic signature since 1988; ii. Cognate xenoliths documenting the active magma chamber and fumaroles display similar He isotopic values (6.58±0.46RA, and 7.31±0.40RA, respectively); iii. OL He isotopic composition is similar to that of other silicate volcanoes of the Arusha region, and comparable to the typical subcontinental lithospheric mantle (SCLM) range (5.2 to 7.0 RA); iv. Ne isotopic ratio of OL is following the MORB signature. Those results are interpreted as showing that 1/ no major modification in the hydrothermal system architecture has occured since 1988 despite major modification of the summit crater morphology, 2/ no contamination by either the atmospheric gases, or crustal material assimilation has occured between the magma chamber and the surface, and 3/ the source of OL and of the other silicate volcanoes in the Arusha region is a SCLM metasomatized by asthenospheric fluids.
Mollex, G., France, L., Furi, E., Bonnet, R., Botcharnikov, R.E., Zimmermann, L., Wilke, S., Deloule, E., Chazot, G., Kazimoto. E.O., Marty, B., Burnard, P.
Abstract: Cognate xenoliths that have been emitted during the last sub-plinian eruption in 2007-08 at Oldoinyo Lengai (OL) represent a unique opportunity to document the igneous processes occuring within the active magma chamber. Detailed petrographic descriptions coupled to a thermobarometric approach, and to the determination of volatile solubility models, allow us to identify the melt evolution at magma chamber conditions, and the storage parameters (P, T). Results indicate that a fresh phonolite melt (~1060°C) was injected into a crustal magma chamber at 11.5 ±3.5 km depth, in agreement with geophysical surveys performed during the eruption. The phonolite contains high volatile contents: 3.2 wt.% H2O and 1.4 wt.% CO2. The liquid line of descent highlights an evolution to nephelinite compositions by cooling down to 880°C. Our results support previous results related to this eruption, and are similar to the historical products emitted during the whole volcano history, allowing us to suggest that no major modification in the plumbing system has occured during the OL evolution. New noble gas results show that: i. fumaroles display constant He isotopic signature since 1988; ii. Cognate xenoliths documenting the active magma chamber and fumaroles display similar He isotopic values (6.58±0.46RA, and 7.31±0.40RA, respectively); iii. OL He isotopic composition is similar to that of other silicate volcanoes of the Arusha region, and comparable to the typical subcontinental lithospheric mantle (SCLM) range (5.2 to 7.0 RA); iv. Ne isotopic ratio of OL is following the MORB signature. Those results are interpreted as showing that 1/ no major modification in the hydrothermal system architecture has occured since 1988 despite major modification of the summit crater morphology, 2/ no contamination by either the atmospheric gases, or crustal material assimilation has occured between the magma chamber and the surface, and 3/ the source of OL and of the other silicate volcanoes in the Arusha region is a SCLM metasomatized by asthenospheric fluids.
Abstract: Cratons represent the oldest preserved lithospheric domains. Their lithosphere (lithospheric mantle welded to overlying Precambrian crystalline basement) is considered to be particularly robust and long living due to the protecting presence of buoyant and rigid “keels” made up of residual harzburgites. In this study, we report new U—Pb zircon ages on crustal xenoliths from the Udachnaya kimberlite in the Siberian craton; this dataset includes samples from both the upper and lower portions of the crust. The zircon ages agree well with model melt-extraction Re-Os ages on refractory peridotite xenoliths from the same pipe; taken together they allow an integrated view of lithosphere formation. Our data reveal that the present day upper crust is Archaean, whereas both the lower crust and the lithospheric mantle yield Palaeoproterozoic ages. Consequently, the deep lithosphere beneath the Siberian craton was not formed in a single time, but grew in two distinct events, one in the late Archean and the other in the Palaeoproterozoic. We propose a two-stage scenario for the formation of the Siberian craton involving delamination and rejuvenation of the Archean lower lithosphere (lower crust and lithospheric mantle) in the Palaeoproterozoic. This demonstrates that craton formation can be a protracted, multi-stage process, and that the present day crust and mantle do not represent complementary reservoirs formed through the same episode.
Abstract: Cratons represent the oldest preserved lithospheric domains. Their lithosphere (lithospheric mantle welded to overlying Precambrian crystalline basement) is considered to be particularly robust and long living due to the protecting presence of buoyant and rigid “keels” made up of residual harzburgites. In this study, we report new U—Pb zircon ages on crustal xenoliths from the Udachnaya kimberlite in the Siberian craton; this dataset includes samples from both the upper and lower portions of the crust. The zircon ages agree well with model melt-extraction Re-Os ages on refractory peridotite xenoliths from the same pipe; taken together they allow an integrated view of lithosphere formation. Our data reveal that the present day upper crust is Archaean, whereas both the lower crust and the lithospheric mantle yield Palaeoproterozoic ages. Consequently, the deep lithosphere beneath the Siberian craton was not formed in a single time, but grew in two distinct events, one in the late Archean and the other in the Palaeoproterozoic. We propose a two-stage scenario for the formation of the Siberian craton involving delamination and rejuvenation of the Archean lower lithosphere (lower crust and lithospheric mantle) in the Palaeoproterozoic. This demonstrates that craton formation can be a protracted, multi-stage process, and that the present day crust and mantle do not represent complementary reservoirs formed through the same episode.
Abstract: Cratons represent the oldest preserved lithospheric domains. Their lithosphere (lithospheric mantle welded to overlying Precambrian crystalline basement) is considered to be particularly robust and long-lived due to the protecting presence of buoyant and rigid “keels” made up of residual harzburgites. Although the cratons are mostly assumed to form in the Archaean, the timing of their formation remains poorly constrained. In particular, there are very few datasets describing concurrently the age of both the crustal and mantle portions of the lithosphere. In this study, we report new U–Pb ages and Hf isotope compositions for zircons in crustal xenoliths from the Udachnaya kimberlite in the central Siberian craton; this dataset includes samples from both the upper and lower portions of the crust. The zircon ages agree well with model melt-extraction Re–Os ages on refractory peridotite xenoliths from the same pipe; taken together they allow an integrated view of lithosphere formation. Our data reveal that the present day upper crust is Archaean, whereas both the lower crust and the lithospheric mantle yield Paleoproterozoic ages. We infer that the deep lithosphere beneath the Siberian craton was not formed in a single Archaean event, but grew in at least two distinct events, one in the late Archaean and the other in the Paleoproterozoic. Importantly, a complete or large-scale delamination and rejuvenation of the Archaean lower lithosphere (lower crust and lithospheric mantle) took place in the Paleoproterozoic. This further demonstrates that craton formation can be a protracted, multi-stage process, and that the present day crust and mantle may not represent complementary reservoirs formed through the same tectono-magmatic event. Further, deep cratonic lithosphere may be less robust and long living than often assumed, with rejuvenation and replacement events throughout its history.
Abstract: Cratons represent the oldest preserved lithospheric domains. Their lithosphere (lithospheric mantle welded to overlying Precambrian crystalline basement) is considered to be particularly robust and long-lived due to the protecting presence of buoyant and rigid “keels” made up of residual harzburgites. Although the cratons are mostly assumed to form in the Archaean, the timing of their formation remains poorly constrained. In particular, there are very few datasets describing concurrently the age of both the crustal and mantle portions of the lithosphere. In this study, we report new U–Pb ages and Hf isotope compositions for zircons in crustal xenoliths from the Udachnaya kimberlite in the central Siberian craton; this dataset includes samples from both the upper and lower portions of the crust. The zircon ages agree well with model melt-extraction Re–Os ages on refractory peridotite xenoliths from the same pipe; taken together they allow an integrated view of lithosphere formation. Our data reveal that the present day upper crust is Archaean, whereas both the lower crust and the lithospheric mantle yield Paleoproterozoic ages. We infer that the deep lithosphere beneath the Siberian craton was not formed in a single Archaean event, but grew in at least two distinct events, one in the late Archaean and the other in the Paleoproterozoic. Importantly, a complete or large-scale delamination and rejuvenation of the Archaean lower lithosphere (lower crust and lithospheric mantle) took place in the Paleoproterozoic. This further demonstrates that craton formation can be a protracted, multi-stage process, and that the present day crust and mantle may not represent complementary reservoirs formed through the same tectono-magmatic event. Further, deep cratonic lithosphere may be less robust and long living than often assumed, with rejuvenation and replacement events throughout its history.
Abstract: Calcic garnets are an important – although somewhat neglected – member of the garnet group. Typically, these mineral are members of complex solid solutions involving largely substitutions in the Fe3+/Al and Si sites and at least eight different end-members. The absolute majority of garnets in this family are Ti-Mg-Fe2+(± Al ± Zr)-bearing andradite transitional to morimotoite and schorlomite. Importantly, these garnets occur as common accessory minerals in a wide range of igneous and rocks, including nepheline syenites, alkali feldspar syenites, melteigite-urtites, nephelinites, melilitolites, melilitites, calcite carbonatites, ultramafic lamprophyres, orangeites, contaminated kimberlites, skarns and rodingites. Calcic garnets have a great capacity for atomic substitutions involving high-field-strength elements and, even more importantly, rare earths (up to 4000 ppm, including Y), Th and U (both up to 100 ppm) at low levels of common Pb. Their (La/Yb)cn ratio varies over two orders of magnitude (from < 0.01 to ~1), making these minerals a sensitive indicator of crystal fractionation, degassing and other magma-evolution processes. Given these unique compositional characteristics and surprising lack of interest in these minerals in the previous literature, we explored the possibility of using calcic garnets as a U-Pb geochronometer. For this purpose, we selected samples of well-crystallized igneous garnet from four very different rock types of different age, including: carbonatite (Afrikanda) from the Devonian Kola Alkaline Province, carbonatite from the Neoproterozoic Belaya Zima complex (Central-Asian mobile belt), ijolite from the Chick Ordovician igneous complex (Central-Asian mobile belt), granitic pegmatite from the Eden Lake complex in the Paleoproterozoic Trans-Hudson orogen, and feldspathoid syenite from the Cinder Lake alkaline complex in the Archean Knee Lake greenstone belt. U-Pb TIMS ages of the studied garnets are mostly concordant and reveal perfect correspondence with reported U-Pb zircon or perovskite ages as well as Sm-Nd isochrone age for these complexes. Therefore we can advertise calcic garnets as a promising tool for U-Pb geochronological studies.
Abstract: The Siberian craton in Russia hosts many of the country's famous diamond mines. The Lomonosov mine, however, occurs within the boundaries of a different craton-the Baltic shield, most of which lies in Europe. Unlike many diamond mines in South Africa, Canada, and Siberia, the Lomonosov deposit is not in a stable Archean geologic setting. Similar to the Argyle diamond mine in Australia, Lomonosov is in a younger Proterozoic orogenic (or mountain-building) region. Fancy pink diamonds at both these localities likely relate to these Proterozoic tectonic processes. Along with other diamond mines in Proterozoic geologic regions, the Lomonosov deposit (and its fancy-color diamond inventory) demonstrates that the diamond potential of these regions should not be overlooked.
Abstract: Heterogeneous, modally banded kyanite-bearing and bimineralic eclogites from the lithospheric mantle, collected at the Roberts Victor Diamond mine (South Africa), show a reaction texture in which kyanite is consumed. Geothermobarometric calculations using measured mineral compositions in Perple_X allowed the construction of a P-T path showing a steep, cool prograde metamorphic gradient of 2 °C/km to reach peak conditions of 5.8 GPa and 890 °C for the kyanite eclogite. The kyanite-out reaction formed bimineralic eclogite and is probably an integral part of the mineralogical evolution of most archetypal bimineralic eclogites at Roberts Victor and potentially elsewhere. The kyanite-out reaction occured at close to peak pressure (5.3 GPa) and was associated with a rise in temperature to 1380 °C. Mass balance calculations show that upon breakdown, the kyanite component is fully accommodated in garnet and omphacite via a reaction system with low water fugacity that required restricted fluid influx from metasomatic sources. The ?18O values of garnets are consistently higher than normal mantle values. Each sample has its characteristic trend of ?18O variance between garnets in the kyanite-bearing sections and those in the bimineralic parts covering a range between 5.1‰ and 6.8‰. No systematic change in O-isotope signature exists across the sample population. Differences in garnet trace element signatures between differing lithologies in the eclogites are significant. Grossular-rich garnets coexisting with kyanite have strong positive Eu-anomalies and low Gd/Yb ratios, while more pyrope-rich garnets in the bimineralic sections have lost their positive Eu-anomaly, have higher Gd/Yb ratios and generally higher heavy rare earth element contents. Garnets in the original kyanite-bearing portions thus reflect the provenance of the rocks as metamorphosed gabbros/troctolites. The kyanite-out reaction was most likely triggered by a heating event in the subcratonic lithosphere. As kyanite contains around 100 ppm of H2O it is suggested that the kyanite-out reaction, once initiated by heating and restricted metasomatic influx, was promoted by the release of water contained in the kyanite. The steep (high-P low-T) prograde P-T path defining rapid compression at low heating rates is atypical for subduction transport of eclogites into the lithospheric mantle. Such a trajectory is best explained in a model where strong lateral compression forces eclogites downward to higher pressures, supporting models of cratonic lithosphere formation by lateral collision and compression.
Abstract: Based on the mineral inclusion content, diamonds from the Argyle Mine, Western Australia, derive primarily (~90%) from eclogitic sources with a minor peridotitic contribution from both harzburgitic and lherzolitic lithologies. The eclogitic inclusions cover a large compositional range and show in part unusually high concentrations of mantle incompatible elements (P, Ti, Na and K). Coherent trends in major elements (e.g., of Ti or Na versus Mg-number) suggest that the eclogitic diamond source was created by a single process, namely igneous fractionation. Calculated bulk rock REEN patterns match a section of oceanic crust reaching from lavas and sheeted dykes to upper gabbros. Positive Eu anomalies for garnet and clinopyroxene, with calculated bulk rock REEN patterns similar to upper (non-layered) gabbros, are strong evidence for plagioclase accumulation, which is characteristic for the gabbroic portions of oceanic crust. Linking previously published oxygen isotope analyses of eclogitic garnet inclusions with their major element composition reveals a correlation between ?18O (mean of +7.2‰) and Na content, consistent with coupled 18O and Na enrichment during low temperature alteration of oceanic crust. The carbon isotopic composition of Argyle eclogitic diamonds forms a normal distribution around a ?13C value of -11‰, indicative of mixing and homogenization of mantle and crustal (organic matter) derived carbon prior to diamond precipitation. Previously published noble gas data on Argyle diamonds support this two component model. Inclusion and nitrogen-in-diamond based thermometry indicate an unusually hot origin of the eclogitic diamond suite, indicative of derivation from the lowermost 25 km (about 180-205 km depth) of the local lithospheric mantle. This is consistent with emplacement of an oceanic protolith during subduction along the Kimberley Craton margin, likely during the Halls Creek Orogeny (about 1.85 Ga). For Argyle eclogitic diamonds the relationship between the rate of platelet degradation and mantle residence temperature indicates that both temperature and strain play an important role in this process. Therefore, ubiquitous platelet degradation and plastic deformation of Argyle diamonds are consistent with derivation from a high temperature environment (softening the diamond lattice) close to the lithosphere-asthenosphere boundary (inducing strain). In combination, the Argyle data set represents a uniquely strong case for a subduction origin of an eclogitic diamond source followed by mixing of mantle and crustal components during diamond formation. Some lherzolitic inclusions show a similarity in incompatible element enrichments (elevated P, Na and K) to the eclogitic suite. The presence of a mildly majoritic lherzolitic garnet further supports a link to eclogitic diamond formation, as very similar majoritic components were found in two eclogitic garnet inclusions. The carbon isotopic composition of peridotitic diamonds shows a mode between -5 to -4 ‰ and a tail extending towards the eclogitic mode (-11 ‰). This suggests the presence of multiple generations of peridotitic diamonds, with indications for an origin linked to the eclogitic suite being restricted to diamonds of lherzolitic paragenesis.
Argyle diamonds – how subduction along the Kimberley Craton edge generated the world's biggest diamond deposit.
Earth and Planetary Science Letters, Vol. 474, pp. 309-321.
Canada, Nunavut
deposit - Jericho
Abstract: During ascent, kimberlites react with the lithospheric mantle, entrain and assimilate xenolithic material, loose volatiles and suffer from syn- and post-magmatic alteration. Consequently, kimberlite rocks deviate heavily from their primary melt. Experiments at 7 GPa, 1300–1480?°C, 10–30 wt% CO2 and 0.46 wt% H2O on a proposed primitive composition from the Jericho kimberlite show that saturation with a lherzolitic mineral assemblage occurs only at 1300–1350?°C for a carbonatitic melt with <8 wt% SiO2 and >35 wt% CO2. At asthenospheric temperatures of >1400?°C, where the Jericho melt stays kimberlitic, this composition saturates only in low-Ca pyroxene, garnet and partly olivine. We hence forced the primitive Jericho kimberlite into multiple saturation with a lherzolitic assemblage by adding a compound peridotite. Saturation in olivine, low- and high-Ca pyroxene and garnet was obtained at 1400–1650 °C (7 GPa), melts are kimberlitic with 18–29 wt% SiO2 + Al2O3, 22.1–24.6 wt% MgO, 15–27 wt% CO2 and 0.4–7.1 wt% H2O; with a trade-off of H2O vs. CO2 and temperature. Melts in equilibrium with high-Ca pyroxene with typical mantle compositions have ?2.5 wt% Na2O, much higher than the commonly proposed 0.1–0.2 wt%. The experiments allow for a model of kimberlite origin in the convective upper mantle, which only requires mantle upwelling that causes melting at the depth where elemental carbon (in metal, diamond or carbide) converts to CO2 (at ?250 km). If primary melts leading to kimberlites contain a few wt% H2O, then adiabatic temperatures of 1400–1500?°C would yield asthenospheric mantle melts that are kimberlitic (>18 wt% SiO2 + Al2O3) but not carbonatitic (<10 wt% SiO2 + Al2O3) in composition, carbonatites only forming 100–200?°C below the adiabat. These kimberlites represent small melt fractions concentrating CO2 and H2O and then acquire part of their chemical signature by assimilation/fractionation during ascent in the subcratonic lithosphere.
Abstract: The characteristics of the sub-continental lithospheric mantle (SCLM) post-date the Siberian plume event (250 Ma) is still unclear; nearly all published data for mantle xenoliths are from a single kimberlite erupt before he Siberian plume (Udachnaya). We report major elements of the whole rock, trace elements data of clinopyroxene and Re-Os isotope and PGE concentration of mantle xenoliths from the Obnazhennaya kimberlite pipe (160 Ma). The Obnazhennaya mantle xenoliths, including spinel harzburgites, spinel dunites, spinel lherzolites, spinel-garnet lherzolite. The spinel harzburgites and dunites have refractory compositions, with 0.23-1.35 wt.% Al2O3, 0.41-3.11 wt.% CaO and 0.00-0.09 wt.% TiO2. Clinopyroxenes in harzburgites and dunites have lower Na2O but higher Cr2O3 contents. Modeling of the Y and Yb contents in clinopyroxenes indicates that the spinel harzburgites and dunites have been subjected to ca. 12-17% degrees of partial melting. The spinel harzburgites and dunites have 187Os/188Os of 0.11227-0.11637, giving a TRD age of 1.6-2.2 Ga. This suggests that old cratonic mantle still existed beneath the Obnazhennaya. In contrast, the lherzolites (both spinel- and spinel-garnet-) have more fertile compositions, containing 2.16-6.55 wt.% Al2O3, 2.91-7.55 wt.% CaO and 0.04-0.15 wt.% TiO2. Both spinel and spinelgarnet lherzolites have more radiogenic 187Os/188Os ratios (0.11931-0.17627), enriched P-PGEs. The higher Al2O3 and Os content and depleted IPGE character of these lherzolites suggest that they were not juvenile mantle accreted by Siberian mantle plume but the refertilized ancient mantle. Therefore, our result suggest that the cratonic mantle beneath the Obnazhennaya has not been replaced by juvenile mantle during the Siberian mantle plume.
Abstract: The characteristics of the sub-continental lithospheric mantle (SCLM) post-date the Siberian plume event (250 Ma) is still unclear; nearly all published data for mantle xenoliths are from a single kimberlite erupt before he Siberian plume (Udachnaya). We report major elements of the whole rock, trace elements data of clinopyroxene and Re-Os isotope and PGE concentration of mantle xenoliths from the Obnazhennaya kimberlite pipe (160 Ma). The Obnazhennaya mantle xenoliths, including spinel harzburgites, spinel dunites, spinel lherzolites, spinel-garnet lherzolite. The spinel harzburgites and dunites have refractory compositions, with 0.23-1.35 wt.% Al2O3, 0.41-3.11 wt.% CaO and 0.00-0.09 wt.% TiO2. Clinopyroxenes in harzburgites and dunites have lower Na2O but higher Cr2O3 contents. Modeling of the Y and Yb contents in clinopyroxenes indicates that the spinel harzburgites and dunites have been subjected to ca. 12-17% degrees of partial melting. The spinel harzburgites and dunites have 187Os/188Os of 0.11227-0.11637, giving a TRD age of 1.6-2.2 Ga. This suggests that old cratonic mantle still existed beneath the Obnazhennaya. In contrast, the lherzolites (both spinel- and spinel-garnet-) have more fertile compositions, containing 2.16-6.55 wt.% Al2O3, 2.91-7.55 wt.% CaO and 0.04-0.15 wt.% TiO2. Both spinel and spinelgarnet lherzolites have more radiogenic 187Os/188Os ratios (0.11931-0.17627), enriched P-PGEs. The higher Al2O3 and Os content and depleted IPGE character of these lherzolites suggest that they were not juvenile mantle accreted by Siberian mantle plume but the refertilized ancient mantle. Therefore, our result suggest that the cratonic mantle beneath the Obnazhennaya has not been replaced by juvenile mantle during the Siberian mantle plume.
Abstract: It has been demonstrated for the first time that the isotopic compositions of carbon (?13C) in magmatic calcites from the Udachnaya–East pipe kimberlite groundmass varies from–2.5 to–1.0‰ (V-PDB), while those of oxygen (?18O) range from 15.0 to 18.2‰ (V-SMOW). The obtained results imply that during the terminal late magmatic and postmagmatic stages of the kimberlite pipe formation, the carbonates in the kimberlite groundmass became successively heavier isotopically, which indicates the hybrid nature of the carbonate component of the kimberlite: it was formed with contributions from mantle and sedimentary marine sources.
Geochimica et Cosmochimica Acta, in press available, 22p.
Africa, South Africa
deposit - Venetia
Abstract: Re-Os and platinum group element analyses are reported for peridotite xenoliths from the 533 Ma Venetia kimberlite cluster situated in the Limpopo Mobile Belt, the Neoarchaean collision zone between the Kaapvaal and Zimbabwe Cratons. The Venetian xenoliths provide a rare opportunity to examine the state of the cratonic lithosphere prior to major regional metasomatic disturbance of Re-Os systematics throughout the Phanerozoic. The 32 studied xenoliths record Si-enrichment that is characteristic of the Kaapvaal lithospheric mantle and can be subdivided into five groups based on Re-Os analyses. The most pristine group I samples (n = 13) display an approximately isochronous relationship and fall on a 3.28 ± 0.17 Ga (95 % conf. int.) reference line that is based on their mean TMA age. This age overlaps with the formation age of the Limpopo crust at 3.35–3.28 Ga. The group I samples derive from ?50 to ?170 km depth, suggesting coeval melt depletion of the majority of the Venetia lithospheric mantle column. Group II and III samples have elevated Re/Os due to Re addition during kimberlite magmatism. Group II has otherwise undergone a similar evolution as the group I samples with overlapping 187Os/188Os at eruption age: 187Os/188OsEA, while group III samples have low Os concentrations, unradiogenic 187Os/188OsEA and were effectively Re-free prior to kimberlite magmatism. The other sample groups (IV and V) have disturbed Re-Os systematics and provide no reliable age information. A strong positive correlation is recorded between Os and Re concentrations for group I samples, which is extended to groups II and III after correction for kimberlite addition. This positive correlation precludes a single stage melt depletion history and indicates coupled remobilisation of Re and Os. The combination of Re-Os mobility, preservation of the isochronous relationship, correlation of 187Os/188Os with degree of melt depletion and lack of radiogenic Os addition puts tight constraints on the formation and subsequent evolution of Venetia lithosphere. First, melt depletion and remobilisation of Re and Os must have occurred within error of the 3.28 Ga mean TMA age. Second, the refractory peridotites contain significant Re despite recording >40 % melt extraction. Third, assuming that Si-enrichment and Re-Os mobility in the Venetia lithospheric mantle were linked, this process must have occurred within ?100 Myr of initial melt depletion in order to preserve the isochronous relationship. Based on the regional geological evolution, we propose a rapid recycling model with initial melt depletion at ?3.35 Ga to form a tholeiitic mafic crust that is recycled at ?3.28 Ga, resulting in the intrusion of a TTG suite and Si-enrichment of the lithospheric mantle. The non-zero primary Re contents of the Venetia xenoliths imply that TRD model ages significantly underestimate the true depletion age even for highly depleted peridotites. The overlap of the ?2.6 Ga TRD ages with the time of the Kaapvaal-Limpopo collision is purely fortuitous and has no geological significance. Hence, this study underlines the importance of scrutiny if age information is to be derived from whole rock Re-Os analyses.
South African Institute of Mining and Metallurgy, Vol. 116, 8, pp. 709-714.
Africa, Botswana
deposit - Karowe
Abstract: Historically, the recovery of large diamonds in conventional treatment plant flow sheets has been associated with dense media separation (DMS). This is attributed mainly to DMS's highly efficient and proven track record in the concentration and separation of ores with variable solids densities. In most instances, DMS has been utilized as a pre-concentration step ahead of any recovery plant, due to its ability and versatility in reducing feed within a specific size range to manageable volumes for downstream X-ray processing and subsequent diamond recovery. The benefit of using carbon-signature-based detection equipment for retrieving large stones upfront in the flow sheet not only equates to earlier recovery of diamonds from the system, but also lessens the exposure of diamond-bearing ore to additional materials handling, pumping, and/or crushing, which has been known to damage or even break diamonds and decrease revenue.
Abstract: The Carboniferous sub-platform Tajno alkaline-carbonatite intrusion is located within a narrow alkaline magmatic belt, which trends E–W from SW Lithuania to NE Poland, along the southern rim of the Mesoproterozoic A–type Mazury Complex. The Tajno pluto–volcanic massif comprises clinopyroxenite cumulates and syenites that are crosscut by carbonatite veins of variable thickness. An emplacement age for the carbonatite has been obtained based on zircon U–Pb and pyrrhotite Re–Os from albitites crosscut by the intrusion. Both ages cluster at 354–345Ma, which corresponds to the Tournaisian Epoch of the Early Carboniferous Period. The carbonatite is 5 to 20Ma younger than the Kola Province, Russian Federation [1]. The current Tajno pluto-volcanic massif lies under ~600m of a Meso–Cenozoic cover. Carbonatite igneous systems are formed by processes of partial melting in metasomatised lithospheric mantle, and are associated with mantle plumes. This implies that a specific geochemical footprint may be spread throughout the host rocks and overlying sedimentary cover by post–emplacement processes. This is of key importance for carbonatite mineral exploration under cover. The Tajno carbonatitic veins do not contain typical accessory minerals (e.g. pyrochlore, perovskite, zirconolite, baddeleyite) that are classically found in other carbonatites. Instead, REE-bearing minerals such as burbankite, parisite, synchysite and bastnaesite are common. This explains its low Nb content. By contrast, fluorite is abundant as cement in the carbonatite breccia.This new study of alkaline-carbonatite rock assemblages is focused on: (1) characterise Tajno's isotopic, REE and HFSE footprint based on petrographic and geochemical observations of apatite and titanite; and (2) increase the understanding of Tajno–type carbonatitic intrusions in the region, and determine if such intrusions can be detected under the sedimentary cover by geochemical techniques. [1] Demaiffe et al.,(2013) The Journal of Geology 12, (1), 91–104
Central European carbonatites under cover: insights for mineral exploration from the Tajno alkaline intrusions, NE Poland.
Abstract: Conventional diamond exploration seldom searches directly for diamonds in rock and soil samples. Instead, it focuses on the search for indicator minerals like chrome spinel, which can be used to evaluate diamond potential. Chrome spinels are preserved as pristine minerals in the early Paleozoic (?465 Ma), hydrothermally altered, Group I No. 30 pipe kimberlite that intruded the Neoproterozoic Qingbaikou strata in Wafangdian, North China Craton (NCC). The characteristics of the chrome spinels were investigated by petrographic observation (BSE imaging), quantitative chemical analysis (EPMA), and Raman spectral analysis. The results show that the chrome spinels are mostly sub-rounded with extremely few grains being subhedral, and these spinels are macrocrystic, more than 500 µm in size. The chrome spinels also have compositional zones: the cores are classified as magnesiochromite as they have distinctly chromium-rich (Cr2O3 up to 66.56 wt%) and titanium-poor (TiO2 < 1 wt%) compositions; and the rims are classified as magnetite as they have chromium-poor and iron-rich composition. In the cores of chrome spinels, compositional variations are controlled by Al3+-Cr3+ isomorphism, which results in a strong Raman spectra peak (A1g mode) varying from 690 cm?1 to 702.9 cm?1. In the rims of chrome spinel, compositional variations result in the A1g peak varying from 660 cm?1 to 672 cm?1. The morphology and chemical compositions indicate that the chrome spinels are mantle xenocrysts. The cores of the spinel are remnants of primary mantle xenocrysts that have been resorbed, and the rims were formed during kimberlite magmatism. The compositions of the cores are used to evaluate the diamond potential of this kimberlite through comparison with the compositions of chrome spinels from the Changmazhuang and No. 50 pipe kimberlites in the NCC. In MgO, Al2O3 and TiO2 versus Cr2O3 plots, the chrome spinels from the Changmazhuang and No. 50 pipe kimberlites are mostly located in the diamond stability field. However, only a small proportion of chrome spinels from No. 30 pipe kimberlite have same behavior, which indicates that the diamond potential of the former two kimberlites is greater than that of the No. 30 pipe kimberlite. This is also supported by compositional zones in the spinel grains: there is with an increase in Fe3+ in the rims, which suggests that the chrome spinels experienced highly oxidizing conditions. Oxidizing conditions may have been imparted by fluids/melts that have a great influence on diamond destruction. Here, we suggest that chrome spinel compositions can be a useful tool for identifying the target for diamond potential in the North China Craton.
Geochimica et Cosmochinica Acta, Vol. 213, pp. 574-592.
Africa, Botswana
deposit - Orapa
Abstract: Major- and trace-element compositions of garnet and clinopyroxene, as well as 87Sr/86Sr in clinopyroxene and ?18O in garnet in eclogite and pyroxenite xenoliths from Orapa, at the western margin of the Zimbabwe craton (central Botswana), were investigated in order to trace their origin and evolution in the mantle lithosphere. Two groups of eclogites are distinguished with respect to 87Sr/86Sr: One with moderate ratios (0.7026-0.7046) and another with 87Sr/86Sr >0.7048 to 0.7091. In the former group, heavy ?18O attests to low-temperature alteration on the ocean floor, while 87Sr/86Sr correlates with indices of low-pressure igneous processes (Eu/Eu?, Mg#, Sr/Y). This suggests relatively undisturbed long-term ingrowth of 87Sr at near-igneous Rb/Sr after metamorphism, despite the exposed craton margin setting. The high-87Sr/86Sr group has mainly mantle-like ?18O and is suggested to have interacted with a small-volume melt derived from an aged phlogopite-rich metasome. The overlap of diamondiferous and graphite-bearing eclogites and pyroxenites over a pressure interval of ?3.2 to 4.9 GPa is interpreted as reflecting a mantle parcel beneath Orapa that has moved out of the diamond stability field, due to a change in geotherm and/or decompression. Diamondiferous eclogites record lower median 87Sr/86Sr (0.7039) than graphite-bearing samples (0.7064) and carbon-free samples (0.7051), suggesting that interaction with the - possibly oxidising - metasome-derived melt caused carbon removal in some eclogites, while catalysing the conversion of diamond to graphite in others. This highlights the role of small-volume melts in modulating the lithospheric carbon cycle. Compared to diamondiferous eclogites, eclogitic inclusions in diamonds are restricted to high FeO and low SiO2, CaO and Na2O contents, they record higher equilibrium temperatures and garnets have mostly mantle-like O isotopic composition. We suggest that this signature was imparted by a sublithospheric melt with contributions from a clinopyroxene-rich source, possibly related to the ca. 2.0 Ga Bushveld event.
Journal of Volcanology and Geothermal Research, Vol. 322, pp. 14-25.
Africa, Tanzania
deposit - Oldoinyo Lengai
Abstract: Volcanic ash leachate studies have been conducted on various volcanoes on Earth, but few have been done on African volcanoes until now. Tephra emissions may affect the environment and the health of people living in this area, and therefore we conducted a first tephra (ash and lapilli sized) leachate study on the Oldoinyo Lengai volcano, situated in northern Tanzania. The recent explosive eruption in 2007-2008 provided us with fresh samples from the first three weeks of the eruption which were used for this study. In addition, we also used a natrocarbonatitic sample from the activity prior to the explosive eruption, as the major activity at Oldoinyo Lengai is natrocarbonatitic. To compare the leaching process affecting the natrocarbonatitic lavas and the tephras from Oldoinyo Lengai, the 2006 natrocarbonatitic lava flow was resampled 5 years after the emplacement and compared to the initial, unaltered composition. Special interest was given to the element fluorine (F), since it is potentially toxic to both humans and animals. A daily intake of fluoride (F?) in drinking water of > 1.5 mg/l can lead to dental fluorosis, and higher concentrations lead to skeletal fluorosis. For this reason, a guideline value for fluoride in drinking water was set by the WHO (2011) to 1.5 mg/l. However, surface waters and groundwaters in the Gregory Rift have elevated fluoride levels of up to 9.12 mg/l, and as a consequence, an interim guideline value for Tanzania has been set at 8 mg/l. The total concentration of fluorine in the samples from the natrocarbonatitic lava flow is high (3.2 wt%), whereas we observed a significant decrease of the fluorine concentration (between 1.7 and 0.5 wt%) in the samples collected three days and three weeks after the onset of the explosive 2007-08 eruption. However, the total amount of water-extractable fluoride is lower in the natrocarbonatitic lavas (319 mg/l) than in the nephelinitic tephra (573-895 mg/l). This is due to the solubility of the different F-bearing minerals. In the natrocarbonatites, fluorine exists predominantly in fluorite (CaF2), and in the early tephra as Na-Mg bearing salts such as neighborite (NaMgF3) and sellaite (MgF2). All these three minerals have very low solubility in water (16-130 mg/l). The later nephelinitic tephras contain surface coating of villiaumite (NaF), which is highly soluble (42,200 mg/l) in water and can thus release the fluoride more readily upon contact with water. Although there is still the need for further data and a more precise study on this topic in Tanzania, we can already draw a first conclusion that the intake of water during or directly following the deposition of the tephra is not advisable and should be avoided, whereas the release of fluoride from the lava flow has less influence on the river waters.-
Bulletin de la Societe Geologique de France *eng, Vol. 188, 1-2, 8p.
Russia, Siberia
deposit - Udachnaya-East
Abstract: The Udachnaya-East pipe in Yakutia in Siberia hosts a unique dry (serpentine-free) body of hypabyssal kimberlite (<0.64wt% H2O), associated with a less dry type of kimberlite and a serpentinized kimberlitic breccia. The dry kimberlite is anomalously rich in salts (Na2O and Cl both up to 6wt%) whereas the slightly less dry and the breccia kimberlite are salt free. Yet the Udachnaya kimberlite is a group-I kimberlite, as is the archetypical kimberlite from Kimberley, South Africa. Samples were studied from the three different types of kimberlite (dry-salty, n=8, non-salty, n=5 and breccia, n=3) regarding their mineralogy, geochemistry, and more specifically their sulfur content. Our results show the salty kimberlite is unprecedentedly rich in sulfur (0.13-0.57wt%) compared to the non-salty kimberlite (0.04-0.12wt%) and the breccia (0.29-0.33wt%). In the salty kimberlite, most of the sulfur is present as sulfates (up to 97% of Stotal) and is disseminated throughout the groundmass in close association with Na-K-bearing carbonates. Sulfates occur within the crystal structure of these Na-K-bearing carbonates as the replacement of (CO3) by (SO3) groups, or as Na- and K-rich sulfates (e.g. aphtitalite, (K,Na)3Na(SO4)2). The associated sulfides are djerfisherite; also Na- and K-rich species. The close association of sulfates and carbonates in these S-rich alkaline rocks suggests that the sulfates crystallized from a mantle-derived magma, a case that has strong implication for the oxygen fugacity of kimberlite magmatism and more generally for the global S budget of the mantle.
Abstract: Kimberlite magmas, the primary source of diamonds, have many features indicative of explosive eruptions and high volatile contents. The main approaches used to establish exsolution of fluid during magma ascent include theoretical modeling and experimental estimates of volatile solubility in kimberlite-like melts. Both approaches are hampered by the poorly constrained composition of kimberlite melts. Resorption features on diamonds are very sensitive to the presence and composition of the kimberlite fluid as well as to temperature and pressure. Here, we use direct evidence from diamond resorption features as a new method for investigating the parameters of fluid exsolution. The method is based on experimental reproduction of diamond resorption in kimberlite melts with and without an exsolved fluid phase. We studied 802 diamonds from two kimberlites (BK1 and AK15) from the Orapa cluster, Botswana. Samples from the BK1 pipe include three lithologies: two coherent kimberlites (CK-A and CK-B) and a pyroclastic kimberlite (massive volcaniclastic kimberlite, MVK). The known depth of diamond samples in each kimberlite lithology allows us to demonstrate an increase in the intensity of kimberlite-induced resorption with depth of diamond recovery in the drill holes. Each kimberlite lithology has a different proportion of diamonds with kimberlite-induced resorption, which is unique in style in each lithology: glossy surfaces in MVK due to reaction with C-O-H fluid, rough corroded surfaces in CK-B due to reaction with volatile-undersaturated melt, and a combination of glossy surfaces with corroded features in CK-A due to an overprint of melt resorption after fluid resorption. Both diamond resorption and kimberlite textures in the BK1 kimberlite show evidence of fluid exsolution only in CK-A and MVK lithologies, but no fluid presence in CK-B. The observed diamond resorption features may be controlled by (1) a temporary separation of the rising magma column into a bubble-rich head and bubble-poor volatile-depleted tail and (2) fluid exsolution at depths greater than decompressional degassing. We discuss how the depth of fluid exsolution from kimberlite melt may affect the diamond grade and the resorption of diamond populations in a kimberlite.
The Australian Gemmologist, Vol. 26, 5&6, pp. 88-99.
South America, Brazil, Minas Gerais
deposit - Alto Paranaiba
Abstract: The authors, in a paper in this journal in 2009, note a puzzle, that in spite of extensive exploration for diamonds by major producers in the Alto Paranaiba region of West Minas Gerais State, Brazil, no primary source, such as kimberlites, for the many diamonds produced since their discovery over 250 years has been found. To answer this puzzle we propose that the diamonds are present within a large extrusive volcanic unit probably derived from the Serra Negra alkaline-carbonatitic complex which comprises a super volcano. This origin fits with the 1995 prediction of Nixon on the future direction of diamona-exploration that extrusive units may contain very large volumes of ore, and that carbonatitic emplacement sources need to be considered. The authors argue, based on available evidence from geology and geophysics, that such an origin is compatible with the known data, but that much additional information is needed to substantiate these ideas. Diamonds of the Alto Paraniaba, Brazil: Nixon's prediction verified?
Journal of Mining Science, Vol. 52, 5, pp. 835-841.
Russia
deposit - Yubilieny
Abstract: The article focuses on seismic monitoring of causes of landslides. Such studies are of great importance in open pit mining in permafrost rocks. Extensive mining-induced impact in combination with natural thawing of permafrost as a consequence of the planet warming may end in catastrophe. The authors describe a procedure for plotting velocity profiles of seismic waves along slopes in the presence of extremely contrast discontinuities conditioned by permafrost rocks. The presented approach enables studying slip surfaces of landslides and detecting potential failure zones where wave velocities are lower due to extensive jointing. The processed field data obtained in the area near Chagan-Uzun settlement in Kosh-Agach district of the Republic of Altai are reported.
Geochimica et Cosmochimica Acta, Vol. 216, pp. 358-371.
Europe, Finland
deposit - Karelian
Abstract: We present high-precision isotope dilution data for Os, Ir, Ru, Pt, Pd and Re in Group I and Group II kimberlites from the Karelian craton, as well as 2 samples of the Premier Group I kimberlite pipe from the Kaapvaal craton. The samples have, on average, 1.38 ppb Pt and 1.33 ppb Pd, with Pt/Pd around unity. These PGE levels are markedly lower, by as much as 80%, than those reported previously for kimberlites from South Africa, Brazil and India, but overlap with PGE results reported recently from Canadian kimberlites. Primitive-mantle-normalised chalcophile element patterns are relatively flat from Os to Pt, but Cu, Ni and, somewhat less so, Au are enriched relative to the PGE (e.g., Cu/Pd > 25.000). Pd/Ir ratios are 3,6 on average, lower than in most other mantle melts. The PGE systematics can be largely explained by two components, (i) harzburgite/lherzolite detritus of the SCLM with relatively high IPGE (Os-Ir-Ru)/PPGE (Rh-Pt-Pd) ratios, and (ii) a melt component that has high PPGE/IPGE ratios. By using the concentrations of iridium in the kimberlites as a proxy for the proportion of mantle detritus in the magma, we estimate that the analysed kimberlites contain 3-27% entrained and partially dissolved detritus from the sub-continental lithospheric mantle, consistent with previous estimates of kimberlites elsewhere (Tappe S. et al., 2016, Chem. Geol. http://dx.doi.org/10.1016/j.chemgeo.2016.08.019). The other major component in the samples is melt, modelled to contain an average of 0.85 ppb Pt and 1.09 ppb Pd. Assuming that Group II kimberlites are derived from relatively metasomatised SCLM, our data suggest that the metasomatised Karelian SCLM is relatively poor in Pt and Pd. If our data are representative of other Group II kimberlites elsewhere, this result could imply that the PGE enrichment in certain continental large igneous provinces, including Bushveld, is not derived from melting of metasomatised SCLM.
Abstract: Mineralogy and geochemistry of the Udirpikonda lamprophyre, located within the Mesoproterozoic diamondiferous Wajrakarur kimberlite field (WKF), towards the western margin of the Paleo-Mesoproterozoic Cuddapah basin are presented. The lamprophyre is characterised by a panidiomorphic-porphyritic texture imparted by clinopyroxene, olivine and biotite set in a groundmass of feldspar and spinel. Olivine occurs as the microphenocrysts with a composition range of Fo87-78. Clinopyroxenes display reverse as well as oscillatory optical zoning and are diopsidic in nature with a variation in the composition from core (Wo47 En28 Fs20Ac5) to rim (Wo46En41Fs11Ac3). Biotite (Mg# < 0.6) is the only mica present and spinels are titano-magnetites showing ulvospinel- magnetite solid solution. Plagioclase is the dominant feldspar with a variable compositional range of An41-8Ab82-56Or33-3. Based on the mineralogy, the lamprophyre can be classified to be of calc-alkaline variety but its geochemistry display mixed signals of both alkaline and calc-alkaline lamprophyres. K2O/Na2O ranges from 1.49 to 2.79, making it distinctly potassic and highlights its shoshonitic character. Moderate Mg# (60-65), Ni (110-200 ppm) and Cr (110-260 ppm) contents in the bulk-rock indicate substantial fractional crystallization of olivine and clinopyroxene. Fractionated chondrite normalized REE patterns (average (La/Yb)N = 37.56) indicates involvement of an enriched mantle source from within the garnet stability field whereas slightly negative Ta-Nb-Ti and Hf anomalies displayed on the primitive mantle normalized multi-element spider gram highlight involvement of a subducted component in the mantle source. Given the spatial disposition of the studied lamprophyre, the age of the emplacement is considered to be coeval with WKF kimberlites (~ 1.1 Ga) and the initial 143Nd/144Nd (0.510065-0.510192) and 87Sr/86Sr (0.705333-0.706223) are strikingly similar to those observed for the Smoky Butte lamproites, Montana, USA. Fluid-related subduction enrichment of the mantle source is apparent from the enriched ratios of La/Nb, Ba/Nb and (Hf/Sm)N, (Ta/La)N < 1. Petrogenetic modelling reveals melt generation from 1 to 2% partial melting of an enriched mantle source that subsequently underwent fractional crystallization. Our study provides geochemical and isotopic evidence for a sub-continental lithospheric mantle (SCLM) modified by subduction and asthenospheric upwelling in the Eastern Dharwar Craton. The partial melting of a resulting heterogeneous Eastern Dharwar Craton SCLM to generate Udiripikonda lamprophyre and Wajrakarur kimberlites has been attributed to the Mesoproterozoic regional lithospheric extension event.
Bulletin de la Societe Geologique de France *eng, Vol. 188, 1-2, 14p.
Russia, Siberia
deposit - Udachnaya
Abstract: Xenoliths brought up by kimberlite magmas are rare samples of otherwise inaccessible lithospheric mantle. Eclogite xenoliths are found in most cratons and commonly show a range of mineral and chemical compositions that can be used to better understand craton formation. This study focuses on five new kyanite-bearing eclogites from the Udachnaya kimberlite pipe (367±5 Ma). They are fine-to coarse-grained and consist mainly of “cloudy” clinopyroxene (cpx) and garnet (grt). The clinopyroxene is Al,Na-rich omphacite while the garnet is Ca-rich, by contrast to typical bi-mineral (cpx+grt) eclogites that contain Fe- and Mg-rich garnets. The Udachnaya kyanite eclogites are similar in modal and major element composition to those from other cratons (Dharwar, Kaapvaal, Slave, West African). The kyanite eclogites have lower REE concentrations than bi-mineral eclogites and typically contain omphacites with positive Eu and Sr anomalies, i.e. a “ghost plagioclase signature”. Because such a signature can only be preserved in non-metasomatised samples, we infer that they were present in the protoliths of the eclogites. It follows that subducted oceanic crust is present at the base of the Siberian craton. Similar compositions and textures are also seen in kyanite eclogites from other cratons, which we view as evidence for an Archean, subduction-like formation mechanism related to craton accretion. Thus, contrary to previous work that classifies all kyanite eclogites as type I (IK), metasomatized by carbonatite/kimberlitic fluids, we argue that some of them, both from this work and those from other cratons, belong to the non-metasomatized type II (IIB). The pristine type IIB is the nearest in composition to protoliths of mantle eclogites because it contains no metasomatic enrichments.
Abstract: The paper discusses questions related to the generation of increasing crustal horizontal compressive stresses compared to the idea of the standard gravitational state at the elastic stage or even from the prevalence of horizontal compression over vertical stress equal to the lithostatic pressure. We consider a variant of superfluous horizontal compression related to internal lithospheric processes occurrin in the crust of orogens, shields, and plates. The vertical ascending movements caused by these motions at the sole of the crust or the lithosphere pertain to these and the concomitant exogenic processes giving rise to denudation and, in particular, to erosion of the surfaces of forming rises. The residual stresses of the gravitational stressed state at the upper crust of the Kola Peninsula have been estimated for the first time. These calculations are based on the volume of sediments that have been deposited in Arctic seas beginning from the Mesozoic. The data speak to the possible level of residual horizontal compressive stresses up to 90 MPa in near-surface crustal units. This estimate is consistent with the results of in situ measurements that have been carried out at the Mining Institute of the Kola Science Center, Russian Academy of Sciences (RAS), for over 40 years. It is possible to forecast the horizontal stress gradient based on depth using our concept on the genesis of horizontal overpressure, and this forecasting is important for studying the formation of endogenic deposits.
Abstract: The paper discusses questions related to the generation of increasing crustal horizontal compressive stresses compared to the idea of the standard gravitational state at the elastic stage or even from the prevalence of horizontal compression over vertical stress equal to the lithostatic pressure. We consider a variant of superfluous horizontal compression related to internal lithospheric processes occurrin in the crust of orogens, shields, and plates. The vertical ascending movements caused by these motions at the sole of the crust or the lithosphere pertain to these and the concomitant exogenic processes giving rise to denudation and, in particular, to erosion of the surfaces of forming rises. The residual stresses of the gravitational stressed state at the upper crust of the Kola Peninsula have been estimated for the first time. These calculations are based on the volume of sediments that have been deposited in Arctic seas beginning from the Mesozoic. The data speak to the possible level of residual horizontal compressive stresses up to 90 MPa in near-surface crustal units. This estimate is consistent with the results of in situ measurements that have been carried out at the Mining Institute of the Kola Science Center, Russian Academy of Sciences (RAS), for over 40 years. It is possible to forecast the horizontal stress gradient based on depth using our concept on the genesis of horizontal overpressure, and this forecasting is important for studying the formation of endogenic deposits.
deposits - Tchiuzo, Anomaly 116, Catoca, Alt Cuilo-4, Cuilo-63, Cucumbi-79.
Abstract: In this study, we compare the major- and trace-element compositions of olivine, garnet, and clinopyroxene that occur as single crystals (142 grains), with those derived from xenoliths (51 samples) from six kimberlites in the Lucapa area, northeastern Angola: Tchiuzo, Anomaly 116, Catoca, Alto Cuilo-4, Alto Cuilo-63 and Cucumbi-79. The samples were analyzed using electron probe microanalysis (EPMA) and laser-ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS). The results suggest different paragenetic associations for these kimberlites in the Lucapa area. Compositional overlap in some of the macrocryst and mantle xenolith samples indicates a xenocrystic origin for some of those macrocrysts. The presence of mantle xenocrysts suggests the possibility of finding diamond. Geothermobarometric calculations were carried out using EPMA data from xenoliths by applying the program PTEXL.XLT. Additional well calibrated single-clinopyroxene thermobarometric calculations were also applied. Results indicate the underlying mantle experienced different equilibration conditions. Subsequent metasomatic enrichment events also support a hypothesis of different sources for the kimberlites. These findings contribute to a better understanding of the petrogenetic evolution of the kimberlites in northeastern Angola and have important implications for diamond exploration.
deposits - Tchiuzo, Anomaly 116, Catoca, Alt Cuilo-4, Cuilo-63, Cucumbi-79.
Abstract: In this study, we compare the major- and trace-element compositions of olivine, garnet, and clinopyroxene that occur as single crystals (142 grains), with those derived from xenoliths (51 samples) from six kimberlites in the Lucapa area, northeastern Angola: Tchiuzo, Anomaly 116, Catoca, Alto Cuilo-4, Alto Cuilo-63 and Cucumbi-79. The samples were analyzed using electron probe microanalysis (EPMA) and laser-ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS). The results suggest different paragenetic associations for these kimberlites in the Lucapa area. Compositional overlap in some of the macrocryst and mantle xenolith samples indicates a xenocrystic origin for some of those macrocrysts. The presence of mantle xenocrysts suggests the possibility of finding diamond. Geothermobarometric calculations were carried out using EPMA data from xenoliths by applying the program PTEXL.XLT. Additional well calibrated single-clinopyroxene thermobarometric calculations were also applied. Results indicate the underlying mantle experienced different equilibration conditions. Subsequent metasomatic enrichment events also support a hypothesis of different sources for the kimberlites. These findings contribute to a better understanding of the petrogenetic evolution of the kimberlites in northeastern Angola and have important implications for diamond exploration.
deposits - Tchiuzo, Anomaly 116, Catoca, Alt Cuilo-4, Cuilo-63, Cucumbi-79.
Abstract: In this study, we compare the major- and trace-element compositions of olivine, garnet, and clinopyroxene that occur as single crystals (142 grains), with those derived from xenoliths (51 samples) from six kimberlites in the Lucapa area, northeastern Angola: Tchiuzo, Anomaly 116, Catoca, Alto Cuilo-4, Alto Cuilo-63 and Cucumbi-79. The samples were analyzed using electron probe microanalysis (EPMA) and laser-ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS). The results suggest different paragenetic associations for these kimberlites in the Lucapa area. Compositional overlap in some of the macrocryst and mantle xenolith samples indicates a xenocrystic origin for some of those macrocrysts. The presence of mantle xenocrysts suggests the possibility of finding diamond. Geothermobarometric calculations were carried out using EPMA data from xenoliths by applying the program PTEXL.XLT. Additional well calibrated single-clinopyroxene thermobarometric calculations were also applied. Results indicate the underlying mantle experienced different equilibration conditions. Subsequent metasomatic enrichment events also support a hypothesis of different sources for the kimberlites. These findings contribute to a better understanding of the petrogenetic evolution of the kimberlites in northeastern Angola and have important implications for diamond exploration.
deposits - Tchiuzo, Anomaly 116, Catoca, Alt Cuilo-4, Cuilo-63, Cucumbi-79.
Abstract: In this study, we compare the major- and trace-element compositions of olivine, garnet, and clinopyroxene that occur as single crystals (142 grains), with those derived from xenoliths (51 samples) from six kimberlites in the Lucapa area, northeastern Angola: Tchiuzo, Anomaly 116, Catoca, Alto Cuilo-4, Alto Cuilo-63 and Cucumbi-79. The samples were analyzed using electron probe microanalysis (EPMA) and laser-ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS). The results suggest different paragenetic associations for these kimberlites in the Lucapa area. Compositional overlap in some of the macrocryst and mantle xenolith samples indicates a xenocrystic origin for some of those macrocrysts. The presence of mantle xenocrysts suggests the possibility of finding diamond. Geothermobarometric calculations were carried out using EPMA data from xenoliths by applying the program PTEXL.XLT. Additional well calibrated single-clinopyroxene thermobarometric calculations were also applied. Results indicate the underlying mantle experienced different equilibration conditions. Subsequent metasomatic enrichment events also support a hypothesis of different sources for the kimberlites. These findings contribute to a better understanding of the petrogenetic evolution of the kimberlites in northeastern Angola and have important implications for diamond exploration.
deposits - Tchiuzo, Anomaly 116, Catoca, Alt Cuilo-4, Cuilo-63, Cucumbi-79.
Abstract: In this study, we compare the major- and trace-element compositions of olivine, garnet, and clinopyroxene that occur as single crystals (142 grains), with those derived from xenoliths (51 samples) from six kimberlites in the Lucapa area, northeastern Angola: Tchiuzo, Anomaly 116, Catoca, Alto Cuilo-4, Alto Cuilo-63 and Cucumbi-79. The samples were analyzed using electron probe microanalysis (EPMA) and laser-ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS). The results suggest different paragenetic associations for these kimberlites in the Lucapa area. Compositional overlap in some of the macrocryst and mantle xenolith samples indicates a xenocrystic origin for some of those macrocrysts. The presence of mantle xenocrysts suggests the possibility of finding diamond. Geothermobarometric calculations were carried out using EPMA data from xenoliths by applying the program PTEXL.XLT. Additional well calibrated single-clinopyroxene thermobarometric calculations were also applied. Results indicate the underlying mantle experienced different equilibration conditions. Subsequent metasomatic enrichment events also support a hypothesis of different sources for the kimberlites. These findings contribute to a better understanding of the petrogenetic evolution of the kimberlites in northeastern Angola and have important implications for diamond exploration.
deposits - Tchiuzo, Anomaly 116, Catoca, Alt Cuilo-4, Cuilo-63, Cucumbi-79.
Abstract: In this study, we compare the major- and trace-element compositions of olivine, garnet, and clinopyroxene that occur as single crystals (142 grains), with those derived from xenoliths (51 samples) from six kimberlites in the Lucapa area, northeastern Angola: Tchiuzo, Anomaly 116, Catoca, Alto Cuilo-4, Alto Cuilo-63 and Cucumbi-79. The samples were analyzed using electron probe microanalysis (EPMA) and laser-ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS). The results suggest different paragenetic associations for these kimberlites in the Lucapa area. Compositional overlap in some of the macrocryst and mantle xenolith samples indicates a xenocrystic origin for some of those macrocrysts. The presence of mantle xenocrysts suggests the possibility of finding diamond. Geothermobarometric calculations were carried out using EPMA data from xenoliths by applying the program PTEXL.XLT. Additional well calibrated single-clinopyroxene thermobarometric calculations were also applied. Results indicate the underlying mantle experienced different equilibration conditions. Subsequent metasomatic enrichment events also support a hypothesis of different sources for the kimberlites. These findings contribute to a better understanding of the petrogenetic evolution of the kimberlites in northeastern Angola and have important implications for diamond exploration.
Formation and evolution of hypabyssal kimberlites from the Siberian craton: part 1 - new insights from cathodluminescence of the carbonates. Anabar and Olenek area
Journal of Asian Earth Sciences, Vol. 145, pt. B, pp. 670-678.
Formation and evolution of hypabyssal kimberlites from the Siberian craton: part 1 - new insights from cathodluminescence of the carbonates. Anabar and Olenek area
Journal of Asian Earth Sciences, Vol. 145, pt. B, pp. 670-678.
Abstract: The primary melt and fluid inclusions in regenerated zonal crystals of olivine and homogeneous phenocrysts of olivine from kimberlites of the Udachnaya-East pipe, were first studied by means of microthermometry, optic and scanning electron microscopy, electron and ion microprobe analysis (SIMS), inductively coupled plasma mass-spectrometry (ICP MSC), and Raman spectroscopy. It was established that olivine crystals were regenerated from silicate-carbonate melts at a temperature of ~1100°C.
Van der Meer, Q., Klaver, M., Reisberg, L., Riches, A. J.V., Davies, G.R.
Preservation of an Archean whole rock Re-Os isochron for the Venetia lithospheric mantle: evidence for rapid crustal recycling and lithosphere stabilization at 3.3 Ga.
Geochimica et Cosmochimica Acta, Vol. 216, pp. 242-263.
Abstract: Eocene paleoclimate reconstructions are rarely accompanied by parallel estimates of CO2 from the same locality, complicating assessment of the equilibrium climate response to elevated CO2. We reconstruct temperature, precipitation, and CO2 from latest middle Eocene (ca. 38 Ma) terrestrial sediments in the posteruptive sediment fill of the Giraffe kimberlite in subarctic Canada. Mutual climatic range and oxygen isotope analyses of botanical fossils reveal a humid-temperate forest ecosystem with mean annual temperatures (MATs) more than 17 °C warmer than present and mean annual precipitation ?4× present. Metasequoia stomatal indices and gas-exchange modeling produce median CO2 concentrations of ?630 and ?430 ppm, respectively, with a combined median estimate of ?490 ppm. Reconstructed MATs are more than 6 °C warmer than those produced by Eocene climate models forced at 560 ppm CO2. Estimates of regional climate sensitivity, expressed as ?MAT per CO2 doubling above preindustrial levels, converge on a value of ?13 °C, underscoring the capacity for exceptional polar amplification of warming and hydrological intensification under modest CO2 concentrations once both fast and slow feedbacks become expressed.
Abstract: Magnesian ilmenite is a common kimberlite indicator mineral, although its use in diamond exploration is still controversial. Complex crystallisation and replacement processes have been invoked to explain the wide compositional and textural ranges of ilmenite found in kimberlites. This work aims to shed light on these processes, as well as their implications for diamond exploration. Petrographic studies were combined for the first time with both major- and trace-element analyses to characterise the ilmenite populations found in xenoliths and xenocrysts in two Angolan kimberlites (Congo-Kasai craton). A multi-stage model describes the evolution of ilmenite in these pipes involving: i) crystallisation of ferric and Mg-rich ilmenite either as metasomatic phases or as megacrysts, both in crustal and in metasomatised mantle domains; ii) kimberlite entrainment and xenolith disaggregation producing at least two populations of ilmenite nodules differing in composition; iii) interaction of both types with the kimberlitic magma during eruption, leading to widespread replacement by Mg-rich ilmenite along grain boundaries and fractures. This process produced similar major-element compositions in ilmenites regardless of their primary (i.e., pre-kimberlitic) origin, although the original enrichment in HFSE (Zr, Hf, Ta, Nb) observed in Fe3 +-rich xenocrysts is preserved. Finally (iv) formation of secondary Mn-ilmenite by interaction with a fluid of carbonatitic affinity or by infiltration of a late hydrothermal fluid, followed in some cases by subsolidus alteration in an oxidising environment. The complexities of ilmenite genesis may lead to misinterpretation of the diamond potential of a kimberlite during the exploration stage if textural and trace-element information is disregarded. Secondary Mg-enrichment of ilmenite xenocrysts is common and is unrelated to reducing conditions that could favour diamond formation/preservation in the mantle. Similarly, Mn-rich ilmenite should be disregarded as a diamond indicator mineral, unless textural studies can prove its primary origin.
Abstract: Magnesian ilmenite is a common kimberlite indicator mineral, although its use in diamond exploration is still controversial. Complex crystallisation and replacement processes have been invoked to explain the wide compositional and textural ranges of ilmenite found in kimberlites. This work aims to shed light on these processes, as well as their implications for diamond exploration. Petrographic studies were combined for the first time with both major- and trace-element analyses to characterise the ilmenite populations found in xenoliths and xenocrysts in two Angolan kimberlites (Congo-Kasai craton). A multi-stage model describes the evolution of ilmenite in these pipes involving: i) crystallisation of ferric and Mg-rich ilmenite either as metasomatic phases or as megacrysts, both in crustal and in metasomatised mantle domains; ii) kimberlite entrainment and xenolith disaggregation producing at least two populations of ilmenite nodules differing in composition; iii) interaction of both types with the kimberlitic magma during eruption, leading to widespread replacement by Mg-rich ilmenite along grain boundaries and fractures. This process produced similar major-element compositions in ilmenites regardless of their primary (i.e., pre-kimberlitic) origin, although the original enrichment in HFSE (Zr, Hf, Ta, Nb) observed in Fe3 +-rich xenocrysts is preserved. Finally (iv) formation of secondary Mn-ilmenite by interaction with a fluid of carbonatitic affinity or by infiltration of a late hydrothermal fluid, followed in some cases by subsolidus alteration in an oxidising environment. The complexities of ilmenite genesis may lead to misinterpretation of the diamond potential of a kimberlite during the exploration stage if textural and trace-element information is disregarded. Secondary Mg-enrichment of ilmenite xenocrysts is common and is unrelated to reducing conditions that could favour diamond formation/preservation in the mantle. Similarly, Mn-rich ilmenite should be disregarded as a diamond indicator mineral, unless textural studies can prove its primary origin.
South African Journal of Geology, Vol. 120, 1, pp. 1-20.
Africa, South Africa
deposit - Jagersfontein
Abstract: Our earlier studies continued in a diligent search for rare ultradeep xenoliths in the kimberlite diatreme at Jagersfontein. The search has met with moderate success insofar as 20 majorite-bearing (decomposed to *gt + lamellar px) xenoliths are identified. Discrete gts (1 to 2 cm), gt-rich layers (2 to 3 cm) in lherzolites, and rare megacrystic gts (>3 cm) from xenoliths characterize the ultradeep suite. Pyroxene lamellae are crystallographically controlled along {111} gt planes, but px may also be prismatic, lensoidal, coarsely graphic, or annular to gt; jigsaw, rather than 120° dihedral textures, are typical. Gt ranges from Pyr68-74 mole% and CaO - Cr2O3 relations, with two exceptions, are distinctly lherzolitic. Cpx37-46 = Wo mole%, Jd 3-19 mole%, with 0.4 to 2.4 wt% Cr2O3; opx = 92 to 95 mole% en, and ol averages 92.5 mole% with maximum wt% 0.1 CaO, 0.4 NiO, and 0.1 Cr2 O3. A new class of 10 ultradeep xenoliths has lamellar spinel (Cr/Cr + Al = 0.74; Mg/Mg + Fe = 0.58) in addition to cpx with gt >3wt% Cr2O3 (c.f. 0.5 to 1.5 for sp-free types). Five samples are texturally linked but are compositional outliers to the central body of data: two are sp hosts (Cr# 0.69, Mg# 0.76) and (Cr# 0.74, Mg# 0.57) to gt (Pyr72) + cpx (Jd14); one is a gt megacryst (Pyr80) with sp (Cr# 57, Mg# 69); and the remaining two are unusually rich in chromium with gt = 7.3 to 8.2 wt% Cr2O3, rimmed by cpx (2.3 to 3.3 wt% Cr2O3). In addition, there are 17 xenoliths with compositional affinities to the ultradeep suite but lacking the texturally diagnostic lamellar intergrowths of cpx in gt are possibly completely equilibrated to gt + irregular cpx. Results from the new collection substantiate our earlier conclusions that the mantle was sampled by the Jagersfontein kimberlite from the lower lithosphere (250 to 350 km) and the transition zone (435 km) with diagnostic high P-T majorite in lherzolite that decomposed to gt + px at one or more interruptive stations (e.g. lithosphere-asthenosphere boundary), and at one or another time, en route to the surface. Homogeneous majorite occurs as diamond inclusions at Jagersfontein but these are eclogitic, leading to the proposition that the source region in the asthenosphere was an unassimilated mixture of lherzolite and eclogite in the Mid-Cretaceous at the time of kimberlite sampling. Important questions arise: Is majorite primordial; did majorite form exclusively from the transition of pyroxene; or did subsequent dissolution into coexisting garnet take place? Why has majorite not been identified in eclogite, nor diamonds of lherzolitic affinity? Does the formation of majorite and the crystallization of encapsulating diamond imply distinct high P-T events?
Abstract: To provide new insights into the origin of megacrysts and metasomatism of the subcontinental lithospheric mantle (SCLM), we present a detailed petrographic and geochemical investigation of clinopyroxene-phlogopite xenoliths and clinopyroxene megacrysts from the Grib kimberlite (Arkhangelsk diamond province, Russia). Clinopyroxene megacrysts and clinopyroxene from clinopyroxene-phlogopite xenoliths have similar petrography, major and trace element compositions, and are therefore classified as Cr-rich megacrysts. Geothermobarometry suggests that Cr-rich clinopyroxenes originate from within the SCLM (3.6-4.7 GPa and 764-922 °C). Phlogopite from clinopyroxene-phlogopite xenoliths have low-Ti and -Cr compositions that overlaps with phlogopite megacrysts from the Grib kimberlite. The clinopyroxene-phlogopite rocks within the SCLM are the main source for Cr-rich clinopyroxene and low-Ti phlogopite megacrysts in the Grib kimberlite matrix. Trace element compositions of studied Cr-rich clinopyroxenes have similar geochemical features to clinopyroxenes megacrysts occurrences worldwide and overlap with clinopyroxenes from phlogopite-garnet peridotite xenoliths from the Grib kimberlite. The strong depletion in Ti, Nb, Ta and to a lesser extent in Zr and Hf in clinopyroxene reflects equilibrium with Ti-oxides, such as ilmenite. The clinopyroxene-phlogopite xenoliths could be the final product of metasomatism of garnet peridotites within the SCLM beneath the Grib kimberlite. The calculated equilibrium of clinopyroxene melt compositions suggests that the metasomatic agents were derived from silicate-bearing kimberlite melts. The presence of veinlets infilled with kimberlitic mineral assemblages in clinopyroxene grains suggests that the clinopyroxene-phlogopite rocks experienced intense interactions with kimberlite melt after their formation, but before their entrainment into the host kimberlite magma. This interaction resulted in the formation of high-Ti and -Cr phlogopite and high-Ti clinopyroxene rims, zones and grains with spongy textures. Finally, we propose the sequence of metasomatic events that occurred in the SCLM and the subsequent formation of the Grib kimberlite.
Physics and Chemistry of Minerals, Vol. 44, 9, pp. 655-667.
Russia, Yakutia
deposit - Mir
Abstract: In this study, the specific features of structural defects of type IaB diamonds from the Mir kimberlite pipe (Yakutian diamondiferous province) have been characterized using FTIR and photoluminescence spectroscopy. Mineral inclusions in these diamonds [olivine (Ol), orthopyroxene (OPx), chromite (Chr), sulphide (Sf)] correspond to associations of peridotite rocks at the base of the lithosphere. Nitrogen content in type IaB diamonds shows significant variations, suggesting different growth media and/or several growth stages. A specific feature of these diamonds is the absence or very small amount of platelets, which may be related to annealing during their long-term residence at the temperatures of the base of the lithosphere. All studied diamonds show the presence of hydrogen defects that are active in IR spectra with an intense line at 3107 cm?1, and additional weaker lines at 3085 and 3237 cm?1, which correlated with high nitrogen content. Type IaB diamonds are also characterized by the presence of nitrogen-nickel luminescence centres S2, S3 and 523.2 nm. This feature distinguishes them from superdeep diamonds with extreme nitrogen aggregation states, which clearly attest to different growth conditions and crystallization media of type IaB diamonds from the Mir kimberlite pipe.
Abstract: A single gem lithospheric diamond with five sulfide inclusions from the Udachnaya kimberlite (Siberia, Russia) has been analyzed non-destructively to track the growth conditions of the diamond. Sulfides are the most abundant mineral inclusions in many lithospheric diamond crystals and are the most favorable minerals to date diamond crystals by Re-Os isotope systematics. Our investigation used non-destructive, micro-techniques, combining X-ray tomography, X-ray fluorescence, X-ray powder diffraction, and Raman spectroscopy. This approach allowed us to determine the spatial distribution of the inclusions, their chemical and mineralogical composition on the microscale, and, finally, the paragenetic association, leaving the diamond host completely unaffected. The sample was also studied by X-ray diffraction topography to characterize the structural defects of the diamond and to obtain genetic information about its growth history. The X-ray topographic images show that the sample investigated exhibits plastic deformation. One set of {111} slip lamellae, corresponding to polysynthetic twinning, affects the entire sample. Chemical data on the inclusions still trapped within the diamond show they are monosulfide solid solutions of Fe, Ni and indicate a peridotitic paragenesis. Micro-X-ray diffraction reveals that the inclusions mainly consist of a polycrystalline aggregate of pentlandite and pyrrothite. A thorough analysis of the Raman data suggests the presence of a further Fe, Ni sulfide, never reported so far in diamonds: mackinawite. The total absence of any oxides in the sulfide assemblage clearly indicates that mackinawite is not simply a “late” alteration of pyrrhotite and pentlandite due to secondary oxidizing fluids entering diamond fractures after the diamond transport to the surface. Instead, it is likely formed as a low-temperature phase that grew in a closed system within the diamond host. It is possible that mackinawite is a more common phase in sulfide assemblages within diamond crystals than has previously been presumed, and that the percentage of mackinawite within a given sulfide assemblage could vary from diamond to diamond and from locality to locality.
Abstract: Diamonds from Juina, Brazil, are well-known examples of superdeep diamond crystals formed under sublithospheric conditions and evidence would indicate their origins lie as deep as the Earth's mantle transition zone and the Lower Mantle. Detailed characterization of these minerals and of inclusions trapped within them may thus provide precious minero-petrogenetic information on their growth history in these inaccessible environments. With the aim of studying non-destructively the structural defects in the entire crystalline volume, two diamond samples from this locality, labelled JUc4 and BZ270, respectively, were studied in transmission mode by means of X-ray Diffraction Topography (XRDT) and micro Fourier Transform InfraRed Spectroscopy (µFTIR). The combined use of these methods shows a good fit between the mapping of spatial distribution of extended defects observed on the topographic images and the µFTIR maps corresponding to the concentration of N and H point defects. The results obtained show that both samples are affected by plastic deformation. In particular, BZ270 shows a lower content of nitrogen and higher deformation, and actually consists of different, slightly misoriented grains that contain sub-grains with a rounded-elongated shape. These features are commonly associated with deformation processes by solid-state diffusion creep under high pressure and high temperature.
45th. Annual Yellowknife Geoscience Forum, p. 2 abstract
Canada, Northwest Territories
deposit - Diavik
Abstract: At Diavik, sustainable development is integrated into everything we do. Our operations provide benefits and opportunities for local communities, businesses, and governments. We work with all our stakeholders to deliver substantial and lasting benefits. The Diavik sustainable development report, is a requirement under the Diavik socio-economic monitoring agreement (SEMA). Through this report information on annual training, employment, business benefits, and community initiatives are available to the public. During this session of the Geoscience discussion, we will be sharing the Diavik Diamond mine performance under the SEMA up to and including December 2016.
45th. Annual Yellowknife Geoscience Forum, p. 4 abstract
Canada, Northwest Territories
deposit - Kelvin, Faraday
Abstract: The Kennady North Project kimberlites are located approximately 280 kilometers east-northeast of Yellowknife, in the Northwest Territories of Canada. The unusual geometry and extent of the kimberlite magmatic system is revealed by renewed exploration drilling activities by Kennady Diamonds since 2012. It has become clear that the system comprises multiple intrusive dykes within which several volcaniclastic bodies have developed, all within 11 kilometres of the Gahcho Kué kimberlite cluster and diamond mine. The detailed exploration of the entire system provides unique evidence for subterranean volcanic conduit growth processes that may have scientific and practical exploration benefits. The identified Kennady North Project volcaniclastic bodies are named Kelvin, Faraday 1, Faraday 2 and Faraday 3, and have complex geometries atypical of the more common subvertical kimberlite pipes. Rather, these pipe-like bodies are inclined between 12 and 30 degrees towards the northwest. Kelvin has sharp angular change in trend towards the north. On-going detailed petrographic studies have shown that the pipes contain layers of complex volcaniclastic units with variable volumes of xenolithic fragments, as well as coherent magmatic layers. The pipe textures include evidence for high energy magma and country rock fragmentation processes typically observed in open volcanic systems. The pipes have developed within a shallow 20 degree northwest dipping kimberlite dyke system. Detailed structural geology studies, using fault observations in oriented and unoriented drill core, have identified at least two important fault-fracture trends. The first fault-fracture system is parallel to the dyke segments, and likely related to the intrusion of the dykes and the regional stress tensor during emplacement. The second fault system is subvertical and north-south striking, parallel to the lithological layering within the metasedimentary country rock. The north-south faults match the contact geometry of the Kelvin pipe’s north-south limb exactly. The dykes have been 3-D modelled along with the pipes. Three possible renditions of the dykes have been created, based on different interpretations of dyke segment continuity. The renditions have been labelled “Optimistic”, “Realistic” and “Pessimistic”. The assumptions made have important implications for developing dyke-type mineral resources. The realistic dyke model defines dyke segments that intersect the Kelvin pipe, and those intersections match geometric trends and irregularities in the pipe shape. The coincidental geometries strongly imply that the pipe development interacted with a penecontemporaneous dyke system. The north-south faults also controlled the local trend of Kelvin pipe development, possibly by enhancing fluid permeability, alteration and brecciation along the faults, connecting from one shallow dipping dyke to the next above. Breccia bodies have been observed on similar dipping dykes at Snap Lake mine that intersect fault structures. We conclude that the pipe development geometry and process is governed by a combination of stress, structure and magmatic fluids, and speculate on the nature of the energy required for fragmentation and development of the pipe at some still unknown depth in the crust.
45th. Annual Yellowknife Geoscience Forum, p. 4 abstract
Canada, Northwest Territories
deposit - Kelvin, Faraday
Abstract: The Kennady North Project kimberlites are located approximately 280 kilometers east-northeast of Yellowknife, in the Northwest Territories of Canada. The unusual geometry and extent of the kimberlite magmatic system is revealed by renewed exploration drilling activities by Kennady Diamonds since 2012. It has become clear that the system comprises multiple intrusive dykes within which several volcaniclastic bodies have developed, all within 11 kilometres of the Gahcho Kué kimberlite cluster and diamond mine. The detailed exploration of the entire system provides unique evidence for subterranean volcanic conduit growth processes that may have scientific and practical exploration benefits. The identified Kennady North Project volcaniclastic bodies are named Kelvin, Faraday 1, Faraday 2 and Faraday 3, and have complex geometries atypical of the more common subvertical kimberlite pipes. Rather, these pipe-like bodies are inclined between 12 and 30 degrees towards the northwest. Kelvin has sharp angular change in trend towards the north. On-going detailed petrographic studies have shown that the pipes contain layers of complex volcaniclastic units with variable volumes of xenolithic fragments, as well as coherent magmatic layers. The pipe textures include evidence for high energy magma and country rock fragmentation processes typically observed in open volcanic systems. The pipes have developed within a shallow 20 degree northwest dipping kimberlite dyke system. Detailed structural geology studies, using fault observations in oriented and unoriented drill core, have identified at least two important fault-fracture trends. The first fault-fracture system is parallel to the dyke segments, and likely related to the intrusion of the dykes and the regional stress tensor during emplacement. The second fault system is subvertical and north-south striking, parallel to the lithological layering within the metasedimentary country rock. The north-south faults match the contact geometry of the Kelvin pipe’s north-south limb exactly. The dykes have been 3-D modelled along with the pipes. Three possible renditions of the dykes have been created, based on different interpretations of dyke segment continuity. The renditions have been labelled “Optimistic”, “Realistic” and “Pessimistic”. The assumptions made have important implications for developing dyke-type mineral resources. The realistic dyke model defines dyke segments that intersect the Kelvin pipe, and those intersections match geometric trends and irregularities in the pipe shape. The coincidental geometries strongly imply that the pipe development interacted with a penecontemporaneous dyke system. The north-south faults also controlled the local trend of Kelvin pipe development, possibly by enhancing fluid permeability, alteration and brecciation along the faults, connecting from one shallow dipping dyke to the next above. Breccia bodies have been observed on similar dipping dykes at Snap Lake mine that intersect fault structures. We conclude that the pipe development geometry and process is governed by a combination of stress, structure and magmatic fluids, and speculate on the nature of the energy required for fragmentation and development of the pipe at some still unknown depth in the crust.
Journal of African Earth Sciences, Vol. 137, pp. 9-21.
Africa, Botswana
deposit - Jwaneng
Abstract: Country rock at Jwaneng Diamond Mine provides a rare insight into the deformational history of the Transvaal Supergroup in southern Botswana. The ca. 235 Ma kimberlite diatremes intruded into late Archaean to Early Proterozoic, mixed, siliciclastic-carbonate sediments, that were subjected to at least three deformational events. The first deformational event (D1), caused by NW-SE directed compression, is responsible for NE-trending, open folds (F1) with associated diverging, fanning, axial planar cleavage. The second deformational event (D2) is probably progressive, involving a clockwise rotation of the principal stress to NE-SW trends. Early D2, which was N-S directed, involved left-lateral, oblique shearing along cleavage planes that developed around F1 folds, along with the development of antithetic structures. Progressive clockwise rotation of far-field forces saw the development of NW-trending folds (F2) and its associated, weak, axial planar cleavage. D3 is an extensional event in which normal faulting, along pre-existing cleavage planes, created a series of rhomboid-shaped, fault-bounded blocks. Normal faults, which bound these blocks, are the dominant structures at Jwaneng Mine. Combined with block rotation and NW-dipping bedding, a horst-like structure on the northwestern limb of a broad, gentle, NE-trending anticline is indicated. The early compressional and subsequent extensional events are consistent throughout the Jwaneng-Ramotswa-Lobatse-Thabazimbi area, suggesting that a large area records the same fault geometry and, consequently, deformational history. It is proposed that Jwaneng Mine is at or near the northernmost limit of the initial, northwards-directed compressional event.
Abstract: Preliminary mineralogical and geochemical studies have been carried out on dolomite marble drill cores from the Bayan Obo REE deposit in China. Three types of apatites and four types of monazites have been identified based on textural features: Type 1 apatite occurs as grains with minor monazite (Type 1 monazite) on its border; Type 2 apatite veinlet shows clusters of assemblages with abundant bastnäsite and parisite at the rim; Type 3 apatite has a linear array associated with fluorite and bastnäsite veinlets. Type 2 monazite occurs as clusters intergrowing with parisite and fluorite. Type 3 and 4 monazites occur as polymineralic (fluorite and bastnäsite) and monomineralic veinlets, respectively. These four types of monazites have similar LREE composition but variable Y content (Y2O3 ranging from below determination limits to 0.7?wt%). The three types of apatites also show different REE content and distribution patterns, ranging from high REE abundance (?REE?+?Y: 27243-251789?ppm) and strong LREE enrichment [(La/Yb)CN ?101] in Type 1, less LREE enrichment [(La/Yb)CN ?8] in Type 2 to relatively low REE abundance (?REE?+?Y: 4323-11175?ppm) but high REE fractionation [(La/Yb)CN ?58] in Type 3. The primary apatite has high Sr (5461-6892?ppm) and REE content, implying a carbonatite origin. The late-stage apatites (Types 2 and 3) show different Sr and REE abundances. Significant differences in their Sr composition (6189?±?573, 6041?±?549 and 3492?±?802 for Types 1-3 samples, respectively) and Y/Ho ratio (20.9?±?0.11, 19.5?±?0.17 and 17.4?±?0.37, respectively) indicate that the three types of apatites may have crystallized from different metasomatic fluids. Multi-stage metasomatism resulted in remobilization and redeposition of primary REE minerals to form the Bayan Obo REE deposit.
Abstract: We report new geological, mineralogical, geochemical and geochronological data about the Katugin Ta-Nb-Y-Zr (REE) deposit, which is located in the Kalar Ridge of Eastern Siberia (the southern part of the Siberian Craton). All these data support a magmatic origin of the Katugin rare-metal deposit rather than the previously proposed metasomatic fault-related origin. Our research has proved the genetic relation between ores of the Katugin deposit and granites of the Katugin complex. We have studied granites of the eastern segment of the Eastern Katugin massif, including arfvedsonite, aegirine-arfvedsonite and aegirine granites. These granites belong to the peralkaline type. They are characterized by high alkali content (up to 11.8?wt% Na2O?+?K2O), extremely high iron content (FeO?/(FeO??+?MgO)?=?0.96-1.00), very high content of most incompatible elements - Rb, Y, Zr, Hf, Ta, Nb, Th, U, REEs (except for Eu) and F, and low concentrations of CaO, MgO, P2O5, Ba, and Sr. They demonstrate negative and CHUR-close ?Nd(t) values of 0.0…?1.9. We suggest that basaltic magmas of OIB type (possibly with some the crustal contamination) represent a dominant part of the granitic source. Moreover, the fluorine-enriched fluid phases could provide an additional source of the fluorine. We conclude that most of the mineralization of the Katugin ore deposit occurred during the magmatic stage of the alkaline granitic source melt. The results of detailed mineralogical studies suggest three major types of ores in the Katugin deposit: Zr mineralization, Ta-Nb-REE mineralization and aluminum fluoride mineralization. Most of the ore minerals crystallized from the silicate melt during the magmatic stage. The accessory cryolites in granites crystallized from the magmatic silicate melt enriched in fluorine. However, cryolites in large veins and lens-like bodies crystallized in the latest stage from the fluorine enriched melt. The zircons from the ores in the aegirine-arfvedsonite granite have been dated at 2055?±?7?Ma. This age is close to the previously published 2066?±?6?Ma zircon age of the aegirine-arfvedsonite granites, suggesting that the formation of the Katugin rare-metal deposit is genetically related to the formation of peralkaline granites. We conclude that Katugin rare-metal granites are anorogenic. They can be related to a Paleoproterozoic (?2.05?Ga) mantle plume. As there is no evidence of the 2.05?Ga mantle plume in other areas of southern Siberia, we suggest that the Katugin mineralization occurred on the distant allochtonous terrane, which has been accreted to Siberian Craton later.
45th. Annual Yellowknife Geoscience Forum, p. 33 abstract
Canada, Northwest Territories
deposit - Darby
Abstract: New geological and geophysical research on Canada’s Rae craton are providing an increasingly good baseline for diamond exploration. This study uses mantle xenoliths and xenocrysts from the Darby property, located ~200 km southwest of the community of Kugaaruk, Nunavut, to provide new information on the lithospheric mantle and diamond potential of the western portion of the central Rae. Peridotite xenoliths containing enough fresh olivine have a median Mg# value of 92.5, indistinguishable from the median value of 92.6 typical of cratonic peridotites world-wide. Only of the 14 peridotitic xenoliths contain fresh garnet. Of these, garnet in one sample is classified as harzburgitic (G10), giving a minimum pressure of 4.7 GPa using the P38 geobarometer (38 mW/m2 model geothermal gradient), while garnets from three peridotites are classified as lherzolitic (G9). 52 garnets picked from concentrate have lherzolitic affinities. Lherzolitic diopsides from kimberlite heavy mineral concentrate yield a lithospheric thickness of ~ 200 km. The four garnet peridotite xenoliths and 49 peridotitic garnets from concentrate yield two distinct modes in mantle sampling depths using Ni thermometry, when projected to the Cpx geotherm. A cluster of samples from the higher Ca/Cr lherzolitic garnets equilibrated at 765 to 920 °C with a group of peridotitic garnets (50 % of xenoliths and 28 % of concentrate) from the lower Ca/Cr lherzolitic garnets with anomalously high Ti concentrations yielding super-adiabatic TNi values The aluminum-in-olivine thermometer applied to olivines filtered to be “garnet facies yielded a mantle sampling portion of the mantle cargo from the diamond stability field. A suite of pyroxenitic xenoliths are a feature of each Darby kimberlite target. New screening techniques indicate that these rocks likely originate close to the crust mantle boundary. Osmium isotope analyses of the Darby peridotites reveal whole-rock Re-depletion ages ranging from Mesoarchean to Paleoproterozoic. The pyroxenite xenoliths have very radiogenic Os isotope compositions and provide the first age information from pyroxenites/“eclogites” beneath the Rae craton. Their resulting Archean whole rock TMA ages are consistent with a Mesoarchean age of the western Central Rae lithosphere older than the lithosphere beneath the Repulse Bay block in the East section of the Rae craton (Liu et al., 2016. Precambrian Research 272). The highly depleted olivine compositions, thick cold lithosphere, and Archean ages of the Darby peridotite xenoliths clearly indicate the presence of 200 km thick cold cratonic lithospheric mantle beneath the western segment of the central Rae craton circa 540 Ma. The Archean model ages of most of the pyroxenites support this, notwithstanding the fact that some of these rocks could be sampling either crust or mantle lithologies very close to the crust-mantle boundary. Mantle sampling took place well into the diamond stability field at Darby.
Abstract: A series of terraces flanking the Lower Orange River in the study area were deposited after ca. 90% of the incision had occurred, thus only the late stage incision/depositional history of this margin is able to be addressed here. Two principal suites of river terraces are distinguished by their palaeo-courses, bedrock strath levels, overall geometry and clast assemblages: an older, higher lying Proto suite and a younger Meso suite. The Proto suite represents a long, post-Eocene, through the Oligocene into the Early Miocene, phase of incision, followed by a prolonged period of aggradation where up to 90 m of fluvial, diamondiferous deposits accumulated during the Early-Middle Miocene. The Meso suite of deposits represents shorter phrases of incision and aggradation in the Pilo-Pleistocene. The Proto and Meso deposits were built in response to both base level rise and increased supply of material from tributaries draining the Great Escarpment locally, with clast assemblage and downstream fining data indicating the latter to be the more important variable. River incision into bedrock is a topic of great interest to fluvial geomorphologists, although most data are derived from active tectonic settings. The incision of a large river into a plateau surface is relatively rare, the best known example being the Colorado River in the young (6 Ma) Grand Canyon. The Orange River in the study area represents a long-lived example of this setting, with the present day dissected topography having evolved from more confined canyon-like walls following the early incision of the Orange River in the Early Tertiary. Although a long-lived incision, the modern channel is not graded in the study area, and is actively incising. The world-wide dataset of incision rates in modern rivers indicates that the Orange River could have completed its entire incision within less than a million years. The continued downcutting of this river so long after the initial incision event is indicative of the roles of intermittent, ongoing epeirogenesis and/or eustatic influences (both of which cannot be proven at this stage), tributary input from the plateau rim (Great Escarpment) or merely the long tag time involved in landscape adjustment following incision into a plateau surface.
Earth and Planetary Science Letters, Vol. 481, pp. 143-153.
Africa, South Africa
deposit - Wesselton
Abstract: Rare garnet crystals from a peridotite xenolith from the Wesselton kimberlite, South Africa, have distinct zones related to two separate episodes of mantle metasomatism. The garnet cores were firstly depleted through melt extraction, then equilibrated during metasomatism by a potentially diamond-forming carbonate-bearing or proto-kimberlitic fluid at 1100-1300?°C and 4.5-5.5 GPa. The garnet rim chemistry, in contrast, is consistent with later overgrowth in equilibrium with a kimberlite at around and . This suggests that the rock was physically moved upwards by up to tens of kilometres between the two metasomatic episodes. Preserved high Ca, Al and Cr contents in orthopyroxenes suggest this uplift was tectonic, rather than magmatic. Diffusion profiles were measured over the transitions between garnet cores and rims using electron microprobe (Mg, Ca, Fe for modelling, plus Cr, Mn, Ti, Na, Al) and nano Secondary Ion Mass Spectrometry (NanoSIMS; 89Y, along with 23Na, Ca, Cr, Fe, Mn and Ti) analyses. The short profile lengths (generally <10 ?m) and low Y concentrations (0.2-60 ppm) make the NanoSIMS approach preferable. Diffusion profiles at the interface between the zones yield constraints on the timescale between the second metasomatic event and eruption of the kimberlite magma that brought the xenolith to the surface. The time taken to form the diffusion profiles is on the order of 25 days to 400 yr, primarily based on modelling of Y diffusion along with Ca, Fe and Mg (multicomponent diffusion) profiles. These timescales are too long to be produced by the interaction of the mantle xenolith with the host kimberlite magma during a single-stage ascent to the crust (hours to days). The samples offer a rare opportunity to study metasomatic processes associated with failed eruption attempts in the cratonic lithosphere.
Abstract: The Bayan Obo ore deposit in Inner Mongolia, North China, the largest-known rare earth element (REE) deposit in the world, is closely associated with carbonatite dykes. Scarce zircon grains, with a wide range of ages and diverse origins, have been extracted from the Wu dyke, a REE-enriched calcitic carbonatite dyke 2?km from the East Ore Body of the Bayan Obo deposit. Three zircon populations were identified based on ages and trace element compositions: 1) Captured zircons with Paleoproterozoic and Archean ages. These zircons have REE patterns and moderate Th/U ratios similar to zircon with silicate inclusions from basement igneous rocks, which have been recognized as contaminants from wall rocks. 2) Carbonatite magmatic zircons with Mesoproterozoic ages. These zircons have high to extremely high Th/U ratios (13-1600), a characteristic signature of the Bayan Obo deposit. Two zircon grains yielded concordant 206Pb/238U ages (1.27?±?0.11?Ga???1.42?±?0.18?Ga) and 208Pb/232Th age (1.26?±?0.20?Ga) with calcite inclusions, indicating that the Wu dyke was emplaced at ca. 1.34?Ga, which coincides with a worldwide generation of Mesoproterozoic kimberlites, lamprophyres, carbonatites, and anorogenic magmatism. 3) Hydrothermal zircons with Caledonian and Triassic ages. The Caledonian zircon has 206Pb/238U age of 381?±?4?Ma and 208Pb/232Th age of 367?±?14?Ma with dolomite inclusion. These evidences are consistent with multiple stages of mineralization, Mesoproterozoic calcite carbonatite magmatism interacted by protracted fluxing of subduction-released Caledonian fluids during the closure of the Palaeo-Asian Ocean, coupled with interaction with the mantle wedge and metasomatism of overlying sedimentary carbonate.
Brazilian Journal of Geology, Vol. 47, 3, pp. 383-401.
South America, Brazil
deposit - Alta Paranaiba
Abstract: Magmatism associated with the Alto Paranaíba structural high comprises kimberlites, kamafugites, and alkaline complexes, forming an approximately 400 x 150 km NW-SE belt in the southern São Francisco Craton. Dating of some intrusions reveals ages between 120 and 75 Ma. Chemical analyses of garnet recovered in alluvium from traditional diamond digging areas indicate peridotitic garnet windows in Três Ranchos and Coromandel. Six hundred and eighty (680) diamonds acquired or recovered during mineral exploration in the digging areas of Romaria, Estrela do Sul, Três Ranchos and Coromandel show unique characteristics, certain populations indicating young, proximal and primary sources (YPP). Analyses of 201 stones from Santo Antônio do Bonito, Santo Inácio and Douradinho rivers alluvium, Coromandel, present no evidence of transport, characterizing a proximal source. Within these river basins, exposures of the Late Cretaceous Capacete Formation basal conglomerate contain mainly small rounded and/or angular quartzite pebbles and of basic and ultrabasic rocks, as well as kimberlite minerals (garnet, ilmenite, spinel, sometimes diamond). A magnetotelluric profile between the Paraná and Sanfranciscana basins shows that the thick underlying lithosphere in the Coromandel region coincides with the peridotitic garnet window and with a diamond population displaying proximal source characteristics. Diamond-bearing kimberlite intrusions occur in different areas of Alto Paranaíba.
Thesis, Phd. Osmania University 258p., http://shodhganga.inflibnet.ac.in/handle/10603/178609.
India, Andhra Pradesh
deposit - Lattavaram, Anumpalli
Abstract: The thesis is organized into six chapters. The first chapter enunciates general concepts of kimberlite geology covering literature, previous work, definitions, classification, mode of occurrence, regional geological history, global and Indian occurrences of kimberlites. The second chapter elucidates the common principles and practices applied and adopted in diamond exploration applicable to the Indian context, to some extent exemplifying the kimberlite clusters of the study area. A six-stage exploration strategy, applicable to Indian geological scenario, has been proposed. The third chapter portrays the general geological setting of the study area comprising Lattavaram and Anumpalli kimberlite clusters along with spatial morphologies of the pipes and various field geological characteristics illustrated through field photographs. The fourth chapter describes various mineralogical and petrographic characteristics observed in the pipes and their associated calcretes as well of the study area emphasising their genetic significance. The fifth chapter characteristically articulates the whole rock geochemistry with the aid of major, trace and rare earth element analyses to depict the classification of the pipes under study. This chapter also demonstrates calcrete geochemistry of calcretes associated with the kimberlite pipes of the study area in detail, perhaps for the first time. The sixth chapter describes the petrogenetic inferences including source region, partial melting, temperature, density and viscosity etc., derived from geochemical analyses and thereby demonstrates the diamond prospectivity of Lattavaram and Anumpalli kimberlite pipes. In a nutshell, this research work aims to present a detailed account of petrography, geochemistry, petrogenesis and diamond prospectivity of kimberlites from Lattavaram and Anumpalli clusters in light of recently discovered pipes. For the first time, petrographic and geochemical analyses of kimberlitic calcretes are presented and interpreted.
Thesis, Phd. Osmania University 258p., http://shodhganga.inflibnet.ac.in/handle/10603/178609.
India, Andhra Pradesh
deposit - Lattavaram, Anumpalli
Abstract: The thesis is organized into six chapters. The first chapter enunciates general concepts of kimberlite geology covering literature, previous work, definitions, classification, mode of occurrence, regional geological history, global and Indian occurrences of kimberlites. The second chapter elucidates the common principles and practices applied and adopted in diamond exploration applicable to the Indian context, to some extent exemplifying the kimberlite clusters of the study area. A six-stage exploration strategy, applicable to Indian geological scenario, has been proposed. The third chapter portrays the general geological setting of the study area comprising Lattavaram and Anumpalli kimberlite clusters along with spatial morphologies of the pipes and various field geological characteristics illustrated through field photographs. The fourth chapter describes various mineralogical and petrographic characteristics observed in the pipes and their associated calcretes as well of the study area emphasising their genetic significance. The fifth chapter characteristically articulates the whole rock geochemistry with the aid of major, trace and rare earth element analyses to depict the classification of the pipes under study. This chapter also demonstrates calcrete geochemistry of calcretes associated with the kimberlite pipes of the study area in detail, perhaps for the first time. The sixth chapter describes the petrogenetic inferences including source region, partial melting, temperature, density and viscosity etc., derived from geochemical analyses and thereby demonstrates the diamond prospectivity of Lattavaram and Anumpalli kimberlite pipes. In a nutshell, this research work aims to present a detailed account of petrography, geochemistry, petrogenesis and diamond prospectivity of kimberlites from Lattavaram and Anumpalli clusters in light of recently discovered pipes. For the first time, petrographic and geochemical analyses of kimberlitic calcretes are presented and interpreted.
Russian Mineralogical Society 200th. Anniversary meeting Oct. 10-13., 4p. Abstract pdf
India
deposit - Pipe-5, Wajrakakarur
Abstract: In an attempt to study the kimberlite indicator minerals (KIMs), loam sampling in the close vicinity of the pipes has been carried out on some kimberlites of the WKF. In this paper, preliminary results of KIMs derived out of loam sampling on one of the WKF pipes at Muligiripalli (pipe-5) are presented. Surface loam sampling has been carried out in the topographically low-lying areas in the close proximity of the pipe outcrop. Four composite samples, at a spacing of ~100 meters, weighing 25 kg each have been collected and sieved through 1 mm mesh. Approximately 5 kg of ‘-1’ fraction has been obtained after sieving which is further subjected to coning and quartering. The material has been subjected to heavy mineral (HM) separation using a manual jig. The HM further screened through Frantz’s isodynamic separator to separate magnetic mineral grains. The HM assemblage includes ilmenite, chromite, Cr-diopside, olivine and sphene. ). To ascertain the kimberlitic nature of the HM grains and thereby to check diamondiferous nature of this pipe, additonal loam sampling to obtain more number of mineral grains to carry out Electron Microprobe Analysis (EPMA) is planned.
Russian Mineralogical Society 200th. Anniversary meeting Oct. 10-13., 4p. Abstract pdf
India
deposit - Pipe-5, Wajrakakarur
Abstract: In an attempt to study the kimberlite indicator minerals (KIMs), loam sampling in the close vicinity of the pipes has been carried out on some kimberlites of the WKF. In this paper, preliminary results of KIMs derived out of loam sampling on one of the WKF pipes at Muligiripalli (pipe-5) are presented. Surface loam sampling has been carried out in the topographically low-lying areas in the close proximity of the pipe outcrop. Four composite samples, at a spacing of ~100 meters, weighing 25 kg each have been collected and sieved through 1 mm mesh. Approximately 5 kg of ‘-1’ fraction has been obtained after sieving which is further subjected to coning and quartering. The material has been subjected to heavy mineral (HM) separation using a manual jig. The HM further screened through Frantz’s isodynamic separator to separate magnetic mineral grains. The HM assemblage includes ilmenite, chromite, Cr-diopside, olivine and sphene. ). To ascertain the kimberlitic nature of the HM grains and thereby to check diamondiferous nature of this pipe, additonal loam sampling to obtain more number of mineral grains to carry out Electron Microprobe Analysis (EPMA) is planned.
45th. Annual Yellowknife Geoscience Forum, p. 65 abstract
Canada, Northwest Territories
deposit - Giraffe
Abstract: Several Lac de Gras kimberlite pipes host thick accumulations of stratified post-eruptive lacustrine sediment and peat. Given the range of Lac de Gras kimberlite emplacement ages, these fills - though rare - provide a unique sedimentary archive of paleoenvironments during the sustained Early Cenozoic “greenhouse” interval, in a high-latitude region otherwise devoid of Phanerozoic sediment cover. Extensive exploration drilling has provided a valuable window into this unique sedimentary record, which would have otherwise remained covered by Quaternary glacial deposits. Our focus to date has been multidisciplinary study of the Giraffe pipe sediment fill: an ~80 m-thick sequence of post-eruptive lacustrine silt overlain by peat, which paints a remarkable picture of a humid-temperate Middle Eocene forest ecosystem on the Canadian Shield. Post-eruptive chronology is provided by interbedded distal tephra horizons, likely sourced from Alaska, that have been dated by glass fission-track and zircon U-Pb techniques. Paleoclimate proxies derived from pollen, wood cellulose oxygen isotopes, and biomarkers converge on reconstructed mean annual temperatures >17 °C warmer than present, with mean winter temperatures above freezing, and mean annual precipitation ~4x present. Two independent reconstructions of CO2 from well preserved conifer foliage suggest that this warming occurred under relatively modest atmospheric CO2 concentrations of 430-630 ppm. These findings provide direct field-based evidence for dramatic past arctic warming at CO2 concentrations that were well within the range of projections under “business-as-usual” emissions scenarios, underscoring the capacity for exceptional polar amplification of climate change under modest CO2 concentrations once both fast and slow feedbacks processes become expressed. Our studies at Giraffe pipe also highlight the scientific value of archived exploration drill core in the Lac de Gras kimberlite field, particularly with respect to pipes that are unremarkable for the purpose of diamond exploration.
Doklady Earth Sciences, Vol. 476, 2, pp. 1155-1158.
Russia, Yakutia
deposit - Udachnaya
Abstract: The crystallographic orientation of three diamonds and 19 olivine inclusions from Udachnaya kimberlite pipe was studied using monocrystal X-ray diffractometry. No epitaxial olivine inclusions were found.
45th. Annual Yellowknife Geoscience Forum, p. 78 abstract
Canada, Northwest Territories, Saskatchewan
deposit - Kelvin, Faraday, Pikoo
Abstract: Many kimberlite ore bodies are relatively small and the presence of overburden can make it challenging to intersect a kimberlite target during exploration drilling. If kimberlite is not intersected during drilling, it can be difficult to decide whether an existing kimberlite body has been missed or whether the geophysical target was not kimberlite. A preliminary spectroscopic study conducted in 2017 provides evidence that kimberlites with sizes exceeding 30 meters hydrate the adjacent country rock. The detection of such ‘hydration halos’ in barren country rock drill cores can provide crucial evidence for the existence of nearby undiscovered kimberlites. To gain a better understanding about the size and morphology of hydration halos around different kimberlite ore bodies, hyperspectral point data were collected from drill cores comprised of crustal rocks recovered in close proximity to known kimberlites (e.g., Kelvin, Farraday, and Pikoo kimberlites). The information obtained as a result of this study will likely serve as a foundation for the development of a rapid, low-cost kimberlite exploration tool that can help evaluate kimberlite potential in areas where kimberlite was not intersected during drilling.
45th. Annual Yellowknife Geoscience Forum, p. 78 abstract
Canada, Northwest Territories, Saskatchewan
deposit - Kelvin, Faraday, Pikoo
Abstract: Many kimberlite ore bodies are relatively small and the presence of overburden can make it challenging to intersect a kimberlite target during exploration drilling. If kimberlite is not intersected during drilling, it can be difficult to decide whether an existing kimberlite body has been missed or whether the geophysical target was not kimberlite. A preliminary spectroscopic study conducted in 2017 provides evidence that kimberlites with sizes exceeding 30 meters hydrate the adjacent country rock. The detection of such ‘hydration halos’ in barren country rock drill cores can provide crucial evidence for the existence of nearby undiscovered kimberlites. To gain a better understanding about the size and morphology of hydration halos around different kimberlite ore bodies, hyperspectral point data were collected from drill cores comprised of crustal rocks recovered in close proximity to known kimberlites (e.g., Kelvin, Farraday, and Pikoo kimberlites). The information obtained as a result of this study will likely serve as a foundation for the development of a rapid, low-cost kimberlite exploration tool that can help evaluate kimberlite potential in areas where kimberlite was not intersected during drilling.
45th. Annual Yellowknife Geoscience Forum, p. 78 abstract
Canada, Northwest Territories, Saskatchewan
deposit - Kelvin, Faraday, Pikoo
Abstract: Many kimberlite ore bodies are relatively small and the presence of overburden can make it challenging to intersect a kimberlite target during exploration drilling. If kimberlite is not intersected during drilling, it can be difficult to decide whether an existing kimberlite body has been missed or whether the geophysical target was not kimberlite. A preliminary spectroscopic study conducted in 2017 provides evidence that kimberlites with sizes exceeding 30 meters hydrate the adjacent country rock. The detection of such ‘hydration halos’ in barren country rock drill cores can provide crucial evidence for the existence of nearby undiscovered kimberlites. To gain a better understanding about the size and morphology of hydration halos around different kimberlite ore bodies, hyperspectral point data were collected from drill cores comprised of crustal rocks recovered in close proximity to known kimberlites (e.g., Kelvin, Farraday, and Pikoo kimberlites). The information obtained as a result of this study will likely serve as a foundation for the development of a rapid, low-cost kimberlite exploration tool that can help evaluate kimberlite potential in areas where kimberlite was not intersected during drilling.
Ackerman, L., Magna, T., Rapprich, V., Upadhyay, D., Kratky, O., Cejkova, B., Erban, V., Kochergina, Y.V., Hrstka, T.
Contrasting petrogenesis of spatially related carbonatites from Samalpatti and Sevattur, Tamil Nadu, India: insights from trace element and isotopic geochemistry.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 31-33.
India
deposit - Samalpatti, Sevattur
Abstract: The Tamil Nadu region in southern India hosts several carbonatite bodies (e.g., Hogenakal, Samalpatti, Sevattur, Pakkanadu-Mulakkadu) which are closely associated with alkaline silicate rocks such as syenites, pyroxenites or dunites (e.g, Kumar et al., 1998; Schleicher et al., 1998; Srivastava, 1998). This is in contrast to the carbonatite occurrences in north-western India associated with the Deccan Trap basalts (e.g., Amba Dongar) or Proterozoic Newania dolomitic carbonatites. We have studied two, spatially related, Neoproterozoic carbonatite-silico(carbonatite) suites in association with alkaline silicate rocks (e.g., pyroxenite, gabbro) from Sevattur and Samalpatti in terms of petrography, chemistry and radiogenic-stable isotopic compositions in order to provide constraints on their genesis and evolution. In these two bodies, several different carbonatite types have been reported previously with striking differences in their trace element and isotopic compositions (Srivastava, 1998; Viladkar and Subramanian, 1995; Schleicher et al., 1998; Pandit et al., 2002). Collected data for previously poorly studied calcite carbonatites from the Sevattur representing the first carbonatite magmas on this locality, indicate similar geochemical characteristics to those of dolomitic carbonatites, such as high LREE/HREE ratios, very high Sr and Ba contents, large amounts of apatite and magnetite, identical Sr-Nd-C-O isotopic compositions. Thus, they were derived from an enriched mantle source without significant post-emplacement modifications through crustal contamination and hydrothermal overprint, in agreement with previous studies (e.g., Schleicher et al., 1998). Detailed microprobe analyses revealed that high levels of some incompatible elements (e.g., REE, Y, Sr, Ba) cannot be accounted by matrix calcite hosting only significant amounts of SrO (~0.6-1.2 wt.%). On the other hand, abundant micro- to nano-scale exsolution lamellae and/or inclusions of mckelveyite-(Nd) appear to host a significant fraction of LREE in parallel with apatite. Distribution of Sr is most likely influenced also by common but heterogeneously dispersed barite and strontianite. Newly acquired as well as detailed inspection of available geochemical data permits distinguish two different types of carbonatites in Samalpatti: (1) Type I similar to Sevattur carbonatites in terms of mineralogy, trace element and radiogenic-stable isotopic compositions and (2) Type II with remarkably low concentrations of REE and other incompatible trace elements, more radiogenic Sr isotopic compositions and extremely variable C–O isotopic values. The petrogenesis of the Type II seems to be intimately associated with the presence of silicocarbonatites and abundant silicate mineral domains. Instead of liquid immiscible separation from a silicate magma, elevated SiO2 contents observed in silico-carbonatites may have resulted from the interaction of primary carbonatitic melts and crustal rocks prior to and/or during magma emplacement. Arguments for such hypothesis include variable, but radiogenic Sr isotopic compositions correlated with SiO2 and other lithophile elements (e.g., Ti, Y, Zr, REE). Calc-silicate marbles present in the Samalpatti area could represent a possible evolved crustal end member for such process due to the inability of common silicate rocks (pyroxenites, granites, diorites) to comply with radiogenic isotopic constraints. The wide range of C-O isotopic compositions found in Samalpatti carbonatites belong to the highest values ever reported for magmatic carbonates and can be best explained by massive hydrothermal interaction with carbonated fluids. Unusual high-Cr silicocarbonatites were discovered at Samalpatti forming centimetre to decimetre-sized enclaves enclosed in pyroxenites with sharp contacts at hand specimen scale. Detailed microprobe analyses revealed peculiar chemical compositions of the Mgamphibole with predominantly sodic composition embaying and replacing Na-Cr-rich pyroxene (kosmochlor), accompanied by the common presence of Cr-spinel and titanite. Such association have been reported for hydrous metasomatism by Na-rich carbonatitic melts at upper mantle conditions (Ali and Arai, 2013). However, the mineralogy and the mode of occurrence of Samalpatti Mg–-r-rich silicocarbonatites argue against such origin. We explain the petrogenesis of these rocks through the reaction of pyroxenites with enriched mantle-derived alkali-CO2-rich melts, as also evidenced by mantle-like O and Hf isotopic compositions.
Major, trace element compositions and Nd, Sr and stable Ca isotopic compositions of carbonatites and alkaline silicate rocks of the Amba Dongar carbonatite complex, India: role of mantle mineralogy and subducted carbonates.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 18.
India
deposit - Amba Dongar
Abstract: Carbonatites, with limited spatial but wide temporal occurrences, are unique igneous rocks with more than 50% modal carbonate. Geochemically carbonatites are characterized by high La/Yb(N) and enrichment in the Ba, Sr concentrations and superchondritic whole-rock Nb/Ta (~35) and Zr/Hf ratios (~60). Most of the global carbonatites are associated with the alkaline silicate rocks and their origin is highly debated. To understand the petrogenesis of carbonatites, we present geochemical and isotopic data, including the first ever measurements of Ca stable isotopes in the ~65 Ma old carbonatites and associated silicate rocks occurring in the Amba Dongar carbonatitic complex in Western India We have performed a detail geochemical and isotopic investigation of the carbonatites and associated silicate rocks occurring in the Amba Dongar carbonatitic complex in Western India. The analysed carbonatites are primarily calcitic and ankeritic in nature. The associated silicate rocks can be classified into two groups, the first being highly Krich and alkaline while the second group is tholeiitic in nature. The high La/Yb(N) ratio of carbonatites are suggestive of low degree partial melting while the enrichment in large ion lithophile elements (LILE) of the silicate rocks suggest that these rocks are derived from a LILE enriched upper mantle source. The carbonatites and the associated alkaline silicate rocks from the Amba Dongar carbonatite complex show overlapping Nd-Sr isotopic compositions with the tholeiitic rocks from the Phenai Mata complex, located approximately 16 km NW of Amba Dongar. Variability in ? 44/40Ca in Hawaiian shield stage tholeiites have been interpreted as evidence of subducted ancient marine carbonates, with very low -44/40Ca, into the Hawaiian plume (Huang et al., 2010). Boron isotopic composition of global carbonatites suggests that subducted crustal components contributed to the mantle source of relatively young carbonatites (<300 Ma old) (Hulett et al., 2016), a signature which should potentially be traceable using Ca isotopes. We report -44/40Ca of carbonatites and associated alkaline silicate rocks from the Amba Dongar complex. The samples were analyzed using a 43Ca-48Ca double spike on a Thermo Fischer Triton Plus Thermal Ionization Mass Spectrometer (TIMS) at IISc. ?44/40Ca in these rocks show a significant variation (~0.6 ‰- (w.r.t. SRM 915a), which is much larger than the variation observed in limited analyses of global carbonatites (Amini et al., 2009). Our external reproducibility, estimated from multiple analyses of NIST standards SRM 915a, SRM 915b and seawater (NASS6), is better than 0.1 - (2SD). ?44/40Ca of the ~65 Ma old Amba Dongar carbonatites shows correlations with Nb/Yb, K/Rb as well as with Sr/Nb, Sr/Zr. These variations suggest the role of phlogopite versus amphibole in the mantle source as well sas subducted carbonates in controlling the ?44/40Ca of these carbonatites.
Textural evidences of late stage carbonate dissolution precipitation and stable isotope exchange re-equilibration in the Kangankunde carbonatite complex, Malawi.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 39-40.
Africa, Malawi
deposit - Kangankunde
Abstract: The Kangankunde carbonatite complex, southern Malawi is an eroded remnant of a carbonatite depocentre belonging to the Lower Cretaceous Chilwa Alkaline Province (Garson and Campbell-Smith, 1965; Karmalkar et al., 2010). The carbonatite complex consists of fenites, carbonated agglomeratic breccias and ankeritic-ferron dolomite carbonatite with sporadic patches of REE minerals. Coarse pegmatitic siderite and ankeritic carbonatite hosts exotic cavities and vugs that contain RE minerals like monazite, synchysite, bastnasite, and florencite-goyazite along with barite and strontianite. Bright green monazite occurs with thick quartz veins and as disseminations within host carbonatites (Garson and Campbell-Smith, 1965; Holt, 1965). Texturally, the host carbonatite exhibits euhedral to subhedral rhombohedra of ankerite-calcite and dolomite set in a fine groundmass. However samples close to mineralized zones show streaky textures, streaming effects and patterns that resemble remobilization and fluidization. Textural evidences such as presence of pseudomorphs containing the REE mineral assemblage, veinlets and drusy cavities indicate that REE mineralization replaced earlier formed carbonates (Wall et al. 1994). SEM micromorphology of such carbonatites show several dissolution-precipitation features indicating that there was a pervasive fluid interaction with the host subsequent to cooling and crystallization. Within cavities and vugs, the precipitation is closely associated with monazite veins and formation of minerals like collinsite, synchysite and rare aragonite (Duraiswami and Shaikh, 2010). Carbon and oxygen isotope ratios were determined on 8 bulk carbonatite powders from Kangankunde using Thermo Fisher Scientific GasBench II, equipped with autosampler (CTC Analytics AG, Zwingen, Switzerland), and coupled to a Delta Plus XP Mass Spectrometer at NGRI, Hyderabad. International Standards NBS-19-1 and NBS-18-1 plus internal standards were used. The internal precision (1s) measured for raw d18O and d13C was 0.04–0.08‰ and 0.03 to 0.06 respectively. The ?13C VS V-PDB show restricted range (-0.31 to -2.76) but ?18O VS V-SMOW values vary widely (8.22 to 24.5). The samples analysed in the present study plot outside the Primary Igneous Carbonatite field (Demény et al., 2004) and are related either to carbo-hydrothermal fluids or alteration of dolomite by a later, cooling, deuteric fluid (Fendley et al., 2017). This study provides conclusive textural evidences (pseudomorphic replacements, atolls, iron-oxide exsolution fringes from dolomite/ankerite, coloform banding, secondary veinlets, etc.) to supports geochemical and stable isotopic inferences about the role of late stage hydrothermal fluids and subsequent alterations in the Kangankunde carbonatite complex (Wall and Mariano, 1996, Wall et al., 1994, Doroshkevich et al., 2009, Fendley et al., 2017).
The Bulhoek carbonatite complex, South Africa: evidence for magmatic crystallization of dolomite at low pressures and the petogenetic implications.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 5-7.
Africa, South Africa
deposit - Bulhoek
Abstract: In many plutonic carbonatite complexes the dominant carbonatite type is calcitic and there is a tendency to assume that dolomitic carbonatites are insignificant relative to calcitic types. While calcitic carbonatites dominate in regions of rifting, e.g. the East African Rift System, dolomitic carbonatites are more abundant in the Archaean Kaapvaal and Zimbabwean Cratons of southern Africa and the Archaean parts of the Canadian Shield (Harmer and Gittins, 1997). The ~1.4Ga Newania carbonatite, the only dolomite carbonatite complex described from India, is located within the Archaean Aravalli Craton (Ray et al., 2013). Increased exploration activity on carbonatites in response to the short-lived 2009-2012 REE boom has highlighted the importance of dolomitic carbonatites as targets for REE (and P) deposits: for example, of the 10 advanced African REE projects (i.e. deposits with a defined resource) associated with carbonatites, 7 are hosted within dolomite carbonatites (Harmer and Nex, 2016). This study reports a detailed petrological study of the Bulhoek Carbonatite Complex, one of a number of carbonatite and alkaline igneous complexes that were emplaced into the central Kaapvaal Craton at 1.4 Ma (Hanson et al., 2006). The Bulhoek Complex comprises three centres of intrusion of magnesian carbonatite into granitic and granophyric components of the 2.05Ga Bushveld Complex over a linear 20 km long zone. At all three centres, areas of fenitised granite enclose sheeted intrusions of dolomitic carbonatite of similar composition and intrusive style. No alkaline silicate magmatic rocks have been in the vicinity of the intrusive centres. Carbonatites were emplaced in three discrete intrusive episodes: initial intrusion was accompanied by significant shattering of the country rocks and produced a sequence of medium-grained, flow foliated dolomite carbonatites (C1) containing clasts of fenitised country rock granites along with xenoliths of fenitised ferrogabbro and magnetite transported from Bushveld Upper Zone cumulates underlying the granites. A second intrusive pulse produced cross-cutting sheets of medium- to coarse-grained dolomitic carbonatite free of xenoliths (C2) that make up the bulk of the carbonatite at each intrusive centre. Evidence that both C1 and C2 carbonatites intruded as crystal-rich mushes include strongly developed sub-vertical foliations, deflection of foliations around large fenite xenoliths and the common occurrence of folded foliations through drag effects at contacts with country rock and in C2 intrusions along contacts with C1 carbonatites.
Noble gas composition of Indian carbonatites ( Amba Dongar, Siriwasan): implications on mantle source compositions and late stage hydrothermal processes.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 10.
India
deposit - Amba Dongar, Siriwasan
Abstract: Within a stepwise crushing study we determined the noble gas composition of several calcite separates, one aegirine and one pyrochlore-aegirine separate of the carbonatite ring dyke complex of Amba Dongar and carbonatite sill complex of Siriwasan, India. Both carbonatites are related to the waning stages of volcanic activity of the Deccan Igneous Province ca. 65 Ma ago. Major observations are a clear radiogenic 4He* and nucleogenic 21Ne* imprint related to insitu production from U and Th in mineral impurities, most likely minute apatite grains. However, in first crushing steps of most calcites from Amba Dongar a well-resolvable mantle neon signal is observed, with lowest air-corrected mantle 21Ne/22Ne-compositions equivalent to the Réunion hotspot mantle source. In case of the aegirine separate from Siriwasan we found a neon composition similar to the Loihi hotspot mantle source. We conclude that previously derived models of a lithospheric mantle source containing recycled components in generation of the carbonatitic magmas from Amba Dongar are obsolete. Instead, the mantle source of both investigated carbonatite complexes is related to a primitive mantle plume source that we tentatively ascribe to the postulated Deccan mantle plume. If, as is commonly suggested, the present location of the Deccan mantle plume source is below Réunion Island, the currently observed more nucleogenic neon isotopic composition of the Réunion hotspot might be obliterated by significant upper mantle contributions, similar to Kilauea Volcano, Hawai’i. In addition, compared with other carbonatite complexes worldwide a rather significant contribution of atmospheric noble gases is observed. This is documented in cut-off 20Ne/22Ne-ratios of ca. 10.2 (Amba Dongar) and 10.45 (Siriwasan) and cut-off 40Ar/36Ar-ratios of about 1500. This atmospheric component likely had been added at shallow levels during the emplacement process. However, understanding the late-stage interaction between atmospheric gases and magmatic mantle fluids still requires further investigation.
Noble gas composition of Indian carbonatites ( Amba Dongar, Siriwasan): implications on mantle source compositions and late stage hydrothermal processes.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 10.
India
deposit - Amba Dongar, Siriwasan
Abstract: Within a stepwise crushing study we determined the noble gas composition of several calcite separates, one aegirine and one pyrochlore-aegirine separate of the carbonatite ring dyke complex of Amba Dongar and carbonatite sill complex of Siriwasan, India. Both carbonatites are related to the waning stages of volcanic activity of the Deccan Igneous Province ca. 65 Ma ago. Major observations are a clear radiogenic 4He* and nucleogenic 21Ne* imprint related to insitu production from U and Th in mineral impurities, most likely minute apatite grains. However, in first crushing steps of most calcites from Amba Dongar a well-resolvable mantle neon signal is observed, with lowest air-corrected mantle 21Ne/22Ne-compositions equivalent to the Réunion hotspot mantle source. In case of the aegirine separate from Siriwasan we found a neon composition similar to the Loihi hotspot mantle source. We conclude that previously derived models of a lithospheric mantle source containing recycled components in generation of the carbonatitic magmas from Amba Dongar are obsolete. Instead, the mantle source of both investigated carbonatite complexes is related to a primitive mantle plume source that we tentatively ascribe to the postulated Deccan mantle plume. If, as is commonly suggested, the present location of the Deccan mantle plume source is below Réunion Island, the currently observed more nucleogenic neon isotopic composition of the Réunion hotspot might be obliterated by significant upper mantle contributions, similar to Kilauea Volcano, Hawai’i. In addition, compared with other carbonatite complexes worldwide a rather significant contribution of atmospheric noble gases is observed. This is documented in cut-off 20Ne/22Ne-ratios of ca. 10.2 (Amba Dongar) and 10.45 (Siriwasan) and cut-off 40Ar/36Ar-ratios of about 1500. This atmospheric component likely had been added at shallow levels during the emplacement process. However, understanding the late-stage interaction between atmospheric gases and magmatic mantle fluids still requires further investigation.
Abstract: We report the concentrations ([Li]) and isotopic compositions of Li in mineral separates and bulk rocks obtained by MC-ICPMS for 14 previously studied garnet and spinel peridotite xenoliths from the Udachnaya kimberlite in the central Siberian craton as well as major and trace element compositions for a new suite of 13 deformed garnet peridotites. The deformed Udachnaya peridotites occur at > 5 GPa; they are metasomatized residues of melt extraction, which as a group experienced greater modal and chemical enrichments than coarse peridotites. We identify two sub-groups of the deformed peridotites: (a) mainly cryptically metasomatized (similar to coarse peridotites) with relatively low modal cpx (< 6%) and garnet (< 7%), low Ca and high Mg#, sinusoidal REE patterns in garnet, and chemically unequilibrated garnet and cpx; (b) modally metasomatized with more cpx and garnet, higher Ca, Fe and Ti, and equilibrated garnet and cpx. The chemical enrichments are not proportional to deformation degrees. The deformation in the lower lithosphere is caused by a combination of localized stress, heating and fluid ingress from the pathways of ascending proto-kimberlite melts, with metasomatic media evolving due to reactions with wall rocks. Mg-rich olivine in spinel and coarse garnet Udachnaya peridotites has 1.2-1.9 ppm Li and ?7Li of 1.2-5.0‰, i.e. close to olivine in equilibrated fertile to depleted off-craton mantle peridotites from literature data, whereas olivine from the deformed peridotites has higher [Li] (2.4-7.5 ppm) and a broader range of ?7Li (1.8-11.6‰), which we attribute to pre-eruption metasomatism. [Li] in opx is higher than in coexisting olivine while ?7LiOl-Opx (?7LiOl ? ?7LiOpx) ranges from ? 6.6 to 7.8‰, indicating disequilibrium inter-mineral [Li] and Li-isotope partitioning. We relate these Li systematics to interaction of lithospheric peridotites with fluids or melts that are either precursors of kimberlite magmatism or products of their fractionation and/or reaction with host mantle. The melts rich in Na and carbonates infiltrated, heated and weakened wall-rock peridotites to facilitate their deformation as well as produce high [Li] and variable, but mainly high, ?7Li in olivine. The carbonate-rich melts preferentially reacted with the opx without achieving inter-mineral equilibrium because opx is consumed by such melts, and because of small volumes and uneven distribution of the metasomatic media, as well as short time spans between the melt infiltration and the capture of the wall-rock fragments by incoming portions of ascending kimberlite magma as xenoliths. Trapped interstitial liquid solidified as cryptic components responsible for high [Li] and the lack of ?7Li balance between olivine and opx, and bulk rocks. Unaltered ?26Mg values (0.20-0.26‰) measured in several olivine separates show no effects of the metasomatism on Mg-isotopes, apparently due to high Mg in the peridotites.
Jadhav, G.N., Viladkar, S.G., Goswami, R., Badhe, K.
Fluid melt inclusions petrography of primary calcites from carbonatites of Amba Dongar, Gujarat India.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 15.
India
deposit - Amba Dongar
Abstract: The Amba Dongar Carbonatite complex consists of sovites which are dominantly composed of calcite along with pyrochlore, phlogopite, apatite, barite, ankerite and haematite and minor opaques such as magnetite, chalcopyrite and pyrite. Two distinct types of texture are present in these carbonatites- a mosaic of equigranular calcite crystals and porphyritic texture. Silicate melt inclusions are observed in primary minerals viz. apatite and calcites. These are small droplets of silicate melt entrapped during the growth of the minerals. In this case carbonatite-alkaline silicate melt inclusions are entrapped predominantly in calcite crystals. Dominantly these calcite host minerals are predominantly containing fluid inclusions along with halite, sylvite and minor nahcolite as daughter crystals. The presence of calcite with nahcolite indicates the coexistence of a Ca-rich, alkali-bearing carbonatite melt phase. The melt inclusions are heated upto 1100 °C and the carbonate melt inclusions appear to be homogenized around 950 °C. This fall within the range of melting temperature of a carbonatite melt. In addition to these, three types of fluid inclusions were also observed in host calcite they are i) monophase, ii) biphase and iii) polyphase types of fluid inclusions. The fluid inclusions contain CO2 gas, Li-K carbonate phases and fergusonite based on Micro-Laser- Raman. Carbon dioxide is the dominant gas phase in most of the fluid inclusions, indicating high temperature and deep mantle source(?). The fluid inclusions have formed from a primary mother liquor that has separated out from the early formed carbonatitic melt. This fluid was either formed just after the formation of melt inclusions or during simultaneous crystallization from a carbonatitic or to be more precise carbonatiticpegmatite melt(?).The presence of both melt and fluid inclusions in these primary calcite host minerals indicates the presence of a carbonatitic-pegmatitic fluid, which must have got separated out from the early formed carbonatite-alkaline silicate magma.
Magna, T., Rapprich, V., Wittke, A., Gussone, N., Upadhyay, D., Mikova, J., Pecskay, Z.
Calcium isotope systematics and K-Ar and U-Pb temporal constraints on the genesis of Sevattur Samalpatti carbonatite silicate alkaline complexes.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 34-35.
India
deposit - Samalpatti, Sevattur
Abstract: We present the first systematic survey of Ca isotope compositions in carbonatites and associated silicate rocks from Samalpatti and Sevattur, two Neoproterozoic complexes in Tamil Nadu, south India. Despite their close geographic proximity, their genesis and post-emplacement histories differ (Ackerman et al. 2017). The Sevattur complex appears to have been derived from an enriched mantle source with a limited post-magmatic disturbance. In contrast, carbonatites from Samalpatti show a record of extensive late-stage post-magmatic overprint, also apparent from unusually heavy C-O isotope compositions in a sub-suite of carbonatites (Ackerman et al. 2017). The mean ?44/40Ca = 0.69 ± 0.10‰ is slightly lighter than the average of fertile, unmetasomatized peridotites at ?44/40Ca = 0.95 ± 0.05‰ (Kang et al. 2017). This difference may attest to the general difference between carbonates and silicates (see Kang et al. 2017). It could also reflect Ca isotope fractionation between isotopically heavy silicate and isotopically light carbonate (e.g., John et al. 2012), though to a somewhat minor extent. This is supported by leaching experiments in this study where the extent of silicate-carbonate fractionation (44/40Casilicate-carbonate) has been investigated. The values at ~0.1-0.2‰ are expectedly lower than those reported earlier (~0.6‰; John et al. 2012) and may reflect high-temperature Ca isotope fractionation. The variability in ?44/40Ca values of carbonatites and silico-carbonatites from the Samalpatti complex is larger (0.70- 1.14‰) and appears to be in accord with extensive post-emplacement disturbance. Significant loss of REE and 13C-18O-enriched signature are combined with high ?44/40Ca values, which could reflect massive exchange with metasomatic aqueous fluids. The 40Kdecay correction was applied to K-rich rocks (syenites, monzonites). Given the antiquity of the complex dated at ca. ~800 Ma (Schleicher et al. 1997) and considering high-K/Ca character of some rocks, the resulting ?44/40Ca800 Myr correction was up to ~+1.2‰. In this regard, it is crucial to constrain the age history of the entire region. The nearby Hogenakal carbonatite body was dated at ~2.4 Ga which is much older than Rb-Sr and Sm-Nd age of Sevattur (Kumar et al. 1998) from the same fault system. We have acquired K-Ar mineral (K-feldspar, biotite, amphibole) and U-Pb zircon data from Sevattur and Samalpatti. The K-Ar ages span a range between ~800 and ~510 Ma (~800 Ma for amphiboles and biotites from silico-carbonatites and mafic silicate rocks and ~570-510 Ma for K-feldspars and biotites from syenites), dating two high-grade regional tectono-thermal overprint events, documented earlier. The complex nature of this process is indicated by concordant U-Pb zircon age at ~2.5 Ga yielded for a melatonalite, for which K-Ar biotite age of ~802 Ma was measured. This fits into the age bracket of basement of the Eastern Dharwar Craton. The age distribution bimodality at ~2.5 Ga and ~800 Ma has been found for several other samples, suggesting a pulsed thermal history of the area, associated with a significant overprint by fluids likely derived from the local crust. Particularly high U concentrations in zircons (thousands ppm), combined with a range of K-Ar ages, attest to such multi-episodic history.
Earth and Planetary Science Letters, Vol. 458, 1, pp. 149-159.
Russia
deposit - Udachnaya
Abstract: Cratons represent the oldest preserved lithospheric domains. Their lithosphere (lithospheric mantle welded to overlying Precambrian crystalline basement) is considered to be particularly robust and long-lived due to the protecting presence of buoyant and rigid “keels” made up of residual harzburgites. Although the cratons are mostly assumed to form in the Archaean, the timing of their formation remains poorly constrained. In particular, there are very few datasets describing concurrently the age of both the crustal and mantle portions of the lithosphere. In this study, we report new U-Pb ages and Hf isotope compositions for zircons in crustal xenoliths from the Udachnaya kimberlite in the central Siberian craton; this dataset includes samples from both the upper and lower portions of the crust. The zircon ages agree well with model melt-extraction Re-Os ages on refractory peridotite xenoliths from the same pipe; taken together they allow an integrated view of lithosphere formation. Our data reveal that the present day upper crust is Archaean, whereas both the lower crust and the lithospheric mantle yield Paleoproterozoic ages. We infer that the deep lithosphere beneath the Siberian craton was not formed in a single Archaean event, but grew in at least two distinct events, one in the late Archaean and the other in the Paleoproterozoic. Importantly, a complete or large-scale delamination and rejuvenation of the Archaean lower lithosphere (lower crust and lithospheric mantle) took place in the Paleoproterozoic. This further demonstrates that craton formation can be a protracted, multi-stage process, and that the present day crust and mantle may not represent complementary reservoirs formed through the same tectono-magmatic event. Further, deep cratonic lithosphere may be less robust and long living than often assumed, with rejuvenation and replacement events throughout its history.
LREE and Nb multi metal potentiality of the Amba Dongar carbonatite complex, Chhota Udepur district, Gujarat.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 43-44.
India
deposit - Amba Dongar
Abstract: Rare earth elements (REE) are used in science innovations, due to their unique magnetic, fluorescent and chemical properties. REE are key components in rnany technological devices, like hybrid rechargeable batteries, catalysts, glass polishing, magnets, lasers, TV colour components, superconductors, ceramics etc. They are in great demand for hybrid cars, CD, cameras and high end defence systems. Similarly, niobium (Nb) finds its usage in diverse high tech applications including atomic energy. With increasing technological applications of REE and Nb, their global demand has enhanced over the years. To keep pace with the current demand, many carbonatite complexes in India including the Amba Dongar were revisited to assess their REE and Nb content. Amba Dongar is a classic carbonatite-alkalic rock complex of the Deccan basalt plateau and is emplaced in close proximity to Narmada rift zone. The main rock types of carbonatite affinity include sovite (calcium carbonatite), ankerite (Fe-Mg•Mn carbonatite), siderite (Fe carbonatite), carbonatite breccia (mixed rock. fragments with carbonate cement) etc. Sovite forms a large ring-dyke (nearly 1.5 km dia.) surrounding an incomplete ring of carbonatite breccia. Plugs of ankeritic carbonatite intrude the sovite. To assess rare metal and REE potential of the carbonatite complex geological and radiometric surveys followed by core drilling were carried out in western part of the complex. Rocks of carbonatite affinity have been intercepted in all the boreholes upto a maximum drilled depth of 150 m. It is for the first time that presence of carbonatite and carbonatite breccia has been reported below central basalt in the Amba Dongar complex. Continuity of carbonatites beyond the drilled depth is inferred. Petromineralogical and X-Ray Diffraction studies indicated presence of REE minerals such as monazite, thorite, cerite, synchisite and bastnasite. Besides, rare earth fluorocarbonates, parisite, florencite, barite, strontianite and columbite have also been reported by earlier investigators. Fairly good amount of pyrochlore (Nb mineral) is also present in all the variants of carbonatite. Detailed chemical analysis core at 1 m interval and of composite samples from every borehole was carried out. The results indicate homogeneity of mineralisation in the entire column upto an explored vertical depth of 120 m. Except a few lean zones, the entire column hosts REE mineralisation of the order of >1% ?REE. Some zones have indicated REE mineralisation of the order of >4 % also. Major element analysis of a composite sample representing a small block (400 m x 100 m x 113 m) indicates 14.69% SiO2, 10.57% Fe2O3, 7 21% MgO, 32.23% CaO, 2.77%, Al2O3, 1.48% P2O5, 2.13% MnO, 0.84% FeO, 0.37% TiO2, 0.95% Na2O, 1.35% K2O, and 23.50% LOI. 1.16% LREE (including 161 ppm HREE), 215 ppm Y, 650 ppm Nb, 310 ppm Th and 467 ppm V appear to be of economic significance. Additionally, presence of high content of Ba (2.65%), Sr (0.50%), Pb (530 ppm), F (1.95%) and Zn (1248 ppm) is also important. Taking into consideration these results, resource estimation of a small block of 400 m x 100 m (0.04 sq. km) with an average depth of 113 m was carried out Inferred REE resources ~140000 tonnes contained in 12.00 million tonne ore have been estimated with an average grade of 1.16% REE. Additionally, this block contains 9,600 tonnes Nb2O5 at an average grade of 0 08 % Nb2O5. These values indicate high potential of Amba Dongar carbonatite complex.
Paleoproterozoic carbonatites Newania and Hogenkkal: geochemical and isotoopic characteristics.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 24.
India
deposit - Newania. Hogenkkal
Abstract: Several carbonatite occurrences ranging in age from Proterozoic to Phanerozoic are known and reported from India. Only two amongst them, the Hogenakkal and Newania carbonatites are Paleoproterozoic in age. The Newania carbonatite body, emplaced within Mesoarchean Untala Granite, comprises predominantly dolomiticcarbonatite and minor ankeritic and sövitic phases, in the chronological order. Only the dolomitic-carbonatites have mantle like C- and O-isotopic characteristics and some authors argue that the ankeritic phase is its alteration product while sövite represents late stage calcite veins. The Pb - Pb geochronology yields high ratios and 2.23 Ga age for the dolomitic carbonatite and extremely high Pb/Pb ratios resulting in an unrealistic 1550 Ma age for the ankeritic phase. Melt residence in an intermediate upper mantle/lower crust reservoir, prior to emplacement, has been postulated for the high Pb/Pb ratios observed in dolomitic carbonatites. The 2.4 Ga Hogenakkal carbonatites occur in the northern part of the Southern Granulite Terrane as small isolated bodies hosted within two sub-parallel pyroxenite dykes within a milieu of Archean charnockites. These are fine to mediumgrained and named as sövite, silicate sövite and melanocratic silicate sövite, based upon calcite or calcite + pyroxene as dominant mineralogy. The C- and O-isotopic ratios for all the varieties are remarkably consistent and represent unmodified mantle values (-5.8 to - 6.7‰ V-PDB and 7.2 to 8.7‰ V-SMOW, respectively). However, diversity in Sr- and Nd-isotopic characteristics suggest both enriched and depleted source characteristics and call for a heterogeneous mantle beneath the SGT. Both the groups do indicate presence of an enriched mantle component during late Archean
Abstract: Systematic closely spaced geological traverses conducted in the year 2010, in Lattavaram Kimberlite Cluster (LKC) of Anantapur district, Andhra Pradesh, India, have led to the discovery of a new kimberlite pipe outcrop in the river bed of Balkamthota Vanka (name of the stream used by local farmers) at its confluence with Penna River, close to Pennahobilam. This new pipe occurs at a distance of 1.5 km in NE direction to hitherto reported pipes-5 and 13 occurring at Muligiripalli and Tummatapalli respectively in the LKC of the Wajrakarur Kimberlite Field (WKF). With this pipe, the total number of kimberlite pipes in the WKF raises to 48, considering all the kimberlites discovered by various public and private organizations so far. Preliminary petrography, geochemistry, petrogenetic aspects and diamond prospectivity of the new occurrence have been presented here. Mineralogically, the kimberlite constitutes olivine macrocrysts, serpentinsed olivine psuedomorphs with xenocrystic ilmenite, phlogopite, perovskite, magnetite, Cr-diopside, garnet along with calcite veins. The kimberlite is classified as hypabyssal macrocrystic calcite- phlogopite kimberlite. Mineralogically, the new kimberlite pipe appears as archetypal Group- I kimberlite however, geochemically; the kimberlite shows character of both Group- I and II varieties, more close to lamproitic character. Although it is too early to comment, based on limited analyses carried out in this study, the diamond potentiality of this pipe is not encouraging; it is noteworthy that it highly warrants detailed investigations involving bulk rock geochemistry and drilling to assess its definite geochemical status, petrogenesis and diamond potentiality.
Abstract: The crystal structure of a new structural variety of loparite (Na0.56Ce0.21La0.14Ca0.06Sr0.03Nd0.02Pr0.01)?=1.03(Ti0.83Nb0.15)?=0.98O3 from the Khibiny alkaline massif, Kola peninsula, Russia, was solved by direct methods and refined to R1 = 0.029 for 492 unique observed reflections with I > 2?(I). The mineral is orthorhombic, Ima2, a = 5.5129(2), b = 5.5129(2) and c = 7.7874(5) Å. Similarly to other perovskite-group minerals with the general formula ABO3, the crystal structure of loparite is based upon a three-dimensional framework of distorted corner-sharing BO6. The A cations are coordinated by 12 oxygen atoms and are situated in distorted cuboctahedral cavities. In contrast to the ideal perovskite-type structure (Pm3?m), the unit cell is doubled along the c axis and the a and b axes are rotated in the ab plane at 45o. The BO6 octahedron displays distortion characteristic for the d0 transition metal cations with the out-of-center shift of the B site. The symmetry reduction is also attributable to the distortion of the BO6 octahedra which are tilted and rotated with respect to the c axis. The occurrence of a new acentric variety of loparite can be explained by the pecularities of its chemical composition characterized by the increased content of Ti compared to the previously studied samples.
Primary carbonate-silicate association in the pelletal lapilli: first direct evidence of carbonated peridotitic mantle source for Amba Dongar carbonatites, Deccan igneous province, India.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 30.
India
deposit - Amba Dongar
Abstract: Pelletal lapilli are discrete sub-spherical clasts with a central fragment mantled by a rim of probable juvenile origin. They typically range in size from <1 mm – 60 mm, and occur as accessory components of pipe-filling volcaniclastic rocks such as kimberlites, carbonatites, kamafugites, melilitites and orangeites. They have been variously referred to as ‘tuffacitic lapilli’, ‘spherical or elliptical lapilli’, ‘Pele’s tears’, ‘spinning droplets’, ‘cored lapilli’, or ‘concentric shelled lapilli. Their presence has been increasing reported from extrusive carbonatite complexes world over; for e.g. Umbria and Latium, Central Italy, Abruzzo and Lucaniae, Southern Italy; Fort Portal and Katwe Kikorongo, Uganda; West Qinling, China; Campo de Calatrava, Spain, along with others. I am reporting here occurrence of pelletal and cored lapilli in the proximity of Amba Dongar carbonatite complex. The lapillus comprises of abundant phenocrysts of olivine, which are typically rimmed by dark brown thick coating. Such phenocrysts (oikocrysts) acquire remarkable roundedness, many of these show central circular fracture. Some of the phenocrysts are broken yet preserving their thick-brown rim. This feature is accentuated where such olivine oikocrysts are welded over groundmass mafics (typically clinorpyroxenes). However, most conspicuous thing is the presence of chrome spinel, which is dispersed as minor octahedra within the olivine, but not found in association with other minerals implying that olivine and chrome spinels are primary phases within the lapilli. There are other smaller droplets forming cored lapilli, which are dominantly composed of carbonates. Mineral chemistry of different phases indicate presence of forsteric (Fo89.20-67.34: Fa32.10-10.71: Tp0.46-0.04); chromium-rich spinel (Chromite55.34-24.86, Spinel31.88-10.16, Magnetite34.13-8.68, Mag. Chromite24.45-0.00, Ulvospinel23.21-0.00, Mag. Ulvospinel7.00-0.00, diopsidic clinopyroxene (Wo45.36-41.41: En40.92-50.60: Fs7.98-15.46), ilmenite (Il76.79-75.10:Ge13.08-14.60:Py1.72-1.08:He9.22-7.26), calcic-plagioclase (An69.36-47.90:Ab48.32- 29.27:Or3.78-1.37), and chlorite (ripidolite/brunsvigite). Discovery of pelletal and cored lapilli in the proximity of Amba Dongar carbonatite complex thus provide first direct evidence of the carbonated peridotitic mantle source for Amba Dongar carbonatites.
Carbonatite breccia: a neglected unit in Amba Dongar distreme, Gujarat, India.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 38.
India
deposit - Amba Dongar
Abstract: Carbonatite breccia forms a major unit in the carbonatite-alkalic diatreme of Amba Dongar. In addition to the innermost part of the ring structure, it also forms small and large plugs outside ring structure in form of discontinuous ring around sövite. It is mainly composed of rounded to sub-angular fragments of basement metamorphics, Bagh sandstones, pre-carbonatite basalt, nephelinite and sövite set in the carbonatitic matrix. Besides rock fragments it also shows presence xenocrystal minerals. Carbonatite breccia is later invaded by sövite, alvikite and ankeritic carbonatite. Thorite, pyrochlore, barite, apatite, fluorite and small amount of REE-minerals were introduced in carbonatite breccia by these later intrusives. Zircon, however seems have been caught up from metamorphic gneisses. Microprobe analyses of all these minerals are given here. In places, carbonatite breccia has been silicified by invading hydrothermal solutions rich in fluorite and silica.
Abstract: The varied lithologic facies and mineralogy resulting from emplacement of syngenetic alkaline, ultramafic and carbonatite (AUC) intrusions are made more diverse by variable weathering and alteration. Ultramafic-carbonatite intrusive complexes are a source for many valuable minerals including diamonds and rare earth element minerals. The intrusive bodies are often difficult to detect in the field due to their paucity, weathering, vegetation, and, in some instances, similarity to country rock, especially in the case of carbonatites among sedimentary carbonates. Remote spectroscopic detection is used extensively for geologic mapping yet has not been applied to differentiating sedimentary and igneous carbonate weathering profiles. Here we document the alteration mineralogy of a newly authenticated melilitite-clan carbonatite occurrence in the Avon Volcanic District in southeast Missouri, USA. The presence of lizardite, vermiculite, phlogopite, and andradite in the weathered crust of calcic and dolomitic carbonatites differentiate them from sedimentary dolomites. We apply field and laboratory spectral measurements to determine the feasibility of humid region AUC remote sensing and classification. Automated humid region detection and classification of carbonatites among sedimentary carbonates is shown to be possible using ratios of absorption features in the 2000-2400?nm range as well as features centered near 680, 900, and 1100?nm due transition metal charge transfer and crystal field splitting in garnet, sheet-silicates, and spinel.
Shitole, A., Sant, D.A., Parvez, I.A., Rangarajan, G., Patel, S., Viladkar, S.G., Murty, A.S.N., Kumari, G.
Shallow seismic studies along Amba Dongar to Sinhada ( longitude 74 3 50E) transect, western India.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 16.
India
deposit - Amba Dongar
Abstract: The microtremor method is applied to map subsurface rheological boundaries (stratigraphic, faults and plutons) is based on strong acoustic impedance across contrasting density of rock/ sediment/ weathered interfaces up to shallow depths along longitude 74° 3'50" E from village Amba Dongar (latitude: 21° 59'N) up to Sinhada village (latitude: 22° 14' N). The 30 km long transect exposes variety of rocks viz., unclassified granite gneisses and metasediments (Precambrian age); sediments belonging to Bagh Group (Late Cretaceous); alkaline - carbonatite plutons and lava flows belonging to Deccan Traps (Late Cretaceous). In all, sixty stations were surveyed along the longitude 74° 3'50" E with spacing of 500 m. H/V spectral ratio technique reveals four rheological interfaces identified by resonant frequencies (fr) ranges 0.2213 to 0.7456 Hz (L1), 1.0102 to 3.076 Hz (L2), 4.8508 to 21.0502 Hz (L3), and 24.5018 to 27.1119 Hz (L4). L1 represents interface between plutons, Precambrian basement rocks; L2 represents interface between Bagh sediments, Deccan Traps and intrusives whereas L3 and L4 captures depth of top most weathered profile. We estimate the depth range for L1 L2 L3 and L4 using equation (h = 110.18fr?1.97) derived based on Deep Banni Core (1764 m deep from surface: DGH record). Deep Banni Core has a distinct interface between Mesozoic rocks and Precambrian basement. The depths are further compared with terrain-based equation. Further, the overall results from the present study are compared with seismic refraction studies along Phangia-Kadipani (NGRI Technical Report, 2003). The subsurface profile across longitude 74° 3'50" E educe faults that bound Bagh Group of rocks with Deccan Trap and Precambrian. We identify two plutons underneath three zones of intrusive viz., Amba Dongar Carbonatite Complex (Station 1 to 8), Tiloda Alkaline (station 33 to 44) and Rumadia Alkaline (station 46 to 51). The present study demarcates the presence of depression over Amba Dongar hill (station 1 to 3), filled by post carbonatite basalt earlier reported by Viladkar et al., (1996 and 2005) suggesting caldera morphology. Similarly, studies identify intrusive-pluton interfaces one, below the Amba Dongar hill, and second between village Tiloda and Rumadia at depth of ~500 m from the surface. Microtremor survey further depicts both basement morphology and thickness of Bagh Group and Deccan Traps.
in: Ferbey, T. Plouffe, A., Hickein, A.S. eds. Indicator minerals in tills and stream sediments of the Canadian Cordillera. Geological Association of Canada Special Paper,, Vol. 50, pp. 175-190.
Canada, British Columbia
carbonatite - Aley, Lonnie, Wicheeda
Abstract: This volume consists of a series of papers of importance to indicator minerals in the Canadian Cordillera. Topics include the glacial history of the Cordilleran Ice Sheet, drift prospecting methods, the evolution of survey sampling strategies, new analytical methods, and recent advances in applying indicators minerals to mineral exploration. This volume fills a notable knowledge gap on the use of indicator minerals in the Canadian Cordillera. We hope that the volume serves as a user guide, encouraging the wider application of indicator minerals by the exploration community.
in: Ferbey, T. Plouffe, A., Hickein, A.S. eds. Indicator minerals in tills and stream sediments of the Canadian Cordillera. Geological Association of Canada Special Paper,, Vol. 50, pp. 175-190.
Canada, British Columbia
carbonatite - Aley, Lonnie, Wicheeda
Abstract: This volume consists of a series of papers of importance to indicator minerals in the Canadian Cordillera. Topics include the glacial history of the Cordilleran Ice Sheet, drift prospecting methods, the evolution of survey sampling strategies, new analytical methods, and recent advances in applying indicators minerals to mineral exploration. This volume fills a notable knowledge gap on the use of indicator minerals in the Canadian Cordillera. We hope that the volume serves as a user guide, encouraging the wider application of indicator minerals by the exploration community.
Simon, S.J., Wei, C.T., Viladkar, S.G., Ellmies, R., Soh, Tamech, L.S., Yang, H., Vatuva, A.
Metamitic U rich pyrochlore from Epembe sovitic carbonatite dyke, NW Namibia.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 12.
Africa, Namibia
deposit - Epembe
Abstract: The Epembe carbonatite dyke is located about 80 km north of Opuwo, NW Namibia. The 10 km long dyke is dominated by massive and banded sövitic carbonatite intrusions. Two distinct type of sövite have been recognized: (1) coarse-grained light grey Sövite I which is predominant in brecciated areas and (2) medium- to fine-grained Sövite II which hosts notable concentrations of pyrochlore and apatite. The contact between the carbonatite and basement gneisses is marked by K-feldspar fenite. The pyrochlore chemistry at Epembe shows a compositional trend from primary magmatic Ca-rich pyrochlore toward late hydrothermal fluid enriched carbonatite phase, giving rise to a remarkable shift in chemical composition and invasion of elements such as Si, U, Sr, Ba, Th and Fe. Enrichment in elements like U, Sr and Th lead to metamictization, alteration and A-site vacancy. It is therefore suggested that the carbonatite successive intrusive phases assimilated primary pyrochlore leading to extreme compositional variation especially around the rims of the pyrochlore. The genesis of the Epembe niobium deposit is linked to the carbonatite magmatism but the mechanism that manifested such niobium rich rock remains unclear and might be formed as a result of cumulate process and/or liquid immiscibility of a carbonate-silicate pair.
Abstract: The Diavik Waste Rock Project consists of laboratory and field experiments developed for the investigation and scale-up of the geochemical evolution of sulfidic mine wastes. As part of this project, humidity cell experiments were conducted to assess the long-term geochemical evolution of a low-sulfide waste rock. Reactive transport modelling was used to assess the significant geochemical processes controlling oxidation of sulfide minerals and their dependence on temperature and sulfide mineral content. The geochemical evolution of effluent from waste rock with a sulfide content of 0.16 wt.% and 0.02 wt.% in humidity cells was simulated with the reactive transport model MIN3P, based on a conceptual model that included constant water flow, sulfide mineral content, sulfide oxidation controlled by the availability of oxidants, and subsequent neutralization reactions with carbonate and aluminosilicate minerals. Concentrations of Ni, Co, Cu, Zn, and SO4 in the humidity cell effluent were simulated using the shrinking core model, which represented the control of oxidant diffusion to the unreacted particle surface in the sulfide oxidation process. The influence of temperature was accounted for using the Arrhenius relation and appropriate activation energy values. Comparison of the experiment results, consisting of waste rock differentiated by sulfide mineral content and temperature, indicated surface area and temperature play important roles in rates of sulfide oxidation and release of sulfate and metals. After the model was calibrated to fit the effluent data from the higher sulfide content cells, subsequent simulations were conducted by adjusting only measured parameters, including sulfide mineral content and surface area.
Abstract: The abundance and distribution of halogens (F, Cl) are rarely recorded in kimberlites and therefore their petrogenetic significance is poorly constrained. Halogens are usually present in kimberlite rocks in the structure of phlogopite and apatite, but their original concentrations are never fully retained due to the effects of alteration. To provide new constraints on the origin and evolution of halogens in kimberlites and their melts, we present a detailed study of the petrography and geochemistry of the late-Cretaceous Group-I (or archetypal) Roger kimberlite (Ekati cluster, Canada). The studied samples contain abundant anhedral-to-euhedral olivine which is set in a crystalline groundmass of monticellite, phlogopite, apatite, spinel (i.e. magnesian ulvöspinel-magnetite (MUM), Mg-magnetite, pleonaste, Cr-spinel), and perovskite along with abundant secondary alteration phases (i.e. serpentine, garnet (andradite-schlorlomite), amakinite ((Fe2 +, Mg, Mn)(OH)2), calcite). The Roger kimberlite is characterised by the highest recorded F-content (up to 2688 ppm) of the Ekati cluster kimberlites, which is reflected by the preservation of F-rich phases, where bultfonteinite (Ca4(Si2O7)(F, OH)2) and fluorite commonly replace olivine. In order to examine the composition and evolution of the kimberlite melt prior to post-magmatic processes, we studied melt inclusions in olivine, Cr-spinel, monticellite and apatite. Primary multiphase melt inclusions in Cr-spinel, monticellite and apatite and secondary inclusions in olivine are shown to contain a diversity of daughter phases and compositions that are dominated by alkali/alkali-earth (Na, K, Ba, Sr)-enriched Ca-Mg-carbonates ± F, Na-K-chlorides and sulphates, phosphates ± REE, spinel, silicates (e.g. olivine, phlogopite, (clino)humite), and sulphides. Although alkali/alkali-earth- and halogen-bearing phases are abundant in melt inclusions, they are generally absent from the kimberlite groundmass, most likely due to ubiquitous effects of syn- and/or post-magmatic alteration (i.e. serpentinisation). Comparisons between halogens and other trace elements of similar compatibility (i.e. F/Nd and Cl/U) in the Roger kimberlite and their respective estimated primitive mantle abundances show that halogens should be a more significant component in kimberlites than typically measured. We propose that fluorine in the Roger kimberlite was magmatic and was redistributed during hydrothermal alteration by Ca-bearing serpentinising fluids to produce the observed bultfonteinite/fluorite assemblages. Based the compositions and daughter mineral assemblages in primary melt inclusions and reconstructed halogen abundances, we suggest that Cr-spinel, monticellite and apatite crystallised from a variably differentiated Si-P-Cl-F-bearing carbonate melt that was enriched in alkalis/alkali-earths and highly incompatible trace elements.
Abstract: Monticellite is a magmatic and/or deuteric mineral that is often present, but widely varying in concentrations in Group-I (or archetypal) kimberlites. To provide new constraints on the petrogenesis of monticellite and its potential significance to kimberlite melt evolution, we examine the petrography and geochemistry of the minimally altered hypabyssal monticellite-rich Leslie (Canada) and Pipe 1 (Finland) kimberlites. In these kimberlites, monticellite (Mtc) is abundant (25-45 vol%) and can be classified into two distinct morphological types: discrete and intergrown groundmass grains (Mtc-I), and replacement of olivine (Mtc-II). Primary multiphase melt inclusions in monticellite, perovskite and Mg-magnetite contain assemblages dominated by alkali (Na, K, Ba, Sr)-enriched Ca-Mg-carbonates, chlorides, phosphates, spinel, silicates (e.g. olivine, phlogopite) and sulphides. These melt inclusions probably represent snapshots of a variably differentiated kimberlite melt that evolved in-situ towards carbonatitic and silica-poor compositions. Although unconstrained in their concentration, the presence of alkali-carbonates and chlorides in melt inclusions suggests they are a more significant component of the kimberlite melt than commonly recorded by whole-rock analyses. We present petrographic and textural evidence showing that pseudomorphic Mtc-II resulted from an in-situ reaction between olivine and the carbonate component of the kimberlite melt in the decarbonation reactio. This reaction is supported by the preservation of abundant primary inclusions of periclase and to a lesser extent Fe-Mg-oxides in monticellite, perovskite and Mg-magnetite. Based on the preservation of primary periclase inclusions, we infer that periclase also existed in the groundmass, but was subsequently altered to brucite. We suggest that CO2 degassing in the latter stages of kimberlite emplacement into the crust is largely driven by the observed reaction between olivine and the carbonate melt. For this reaction to proceed, CO2 should be removed (i.e. degassed), which will cause further reaction and additional degassing in response to this chemical system change (Le Chatelier's principle). Our study demonstrates that these proposed decarbonation reactions may be a commonly overlooked process in the crystallisation of monticellite and exsolution of CO2, which may in turn contribute to the explosive eruption and brecciation processes that occur during kimberlite magma emplacement and pipe formation.
Abstract: Monticellite is a magmatic and/or deuteric mineral that is often present, but widely varying in concentrations in Group-I (or archetypal) kimberlites. To provide new constraints on the petrogenesis of monticellite and its potential significance to kimberlite melt evolution, we examine the petrography and geochemistry of the minimally altered hypabyssal monticellite-rich Leslie (Canada) and Pipe 1 (Finland) kimberlites. In these kimberlites, monticellite (Mtc) is abundant (25-45 vol%) and can be classified into two distinct morphological types: discrete and intergrown groundmass grains (Mtc-I), and replacement of olivine (Mtc-II). Primary multiphase melt inclusions in monticellite, perovskite and Mg-magnetite contain assemblages dominated by alkali (Na, K, Ba, Sr)-enriched Ca-Mg-carbonates, chlorides, phosphates, spinel, silicates (e.g. olivine, phlogopite) and sulphides. These melt inclusions probably represent snapshots of a variably differentiated kimberlite melt that evolved in-situ towards carbonatitic and silica-poor compositions. Although unconstrained in their concentration, the presence of alkali-carbonates and chlorides in melt inclusions suggests they are a more significant component of the kimberlite melt than commonly recorded by whole-rock analyses. We present petrographic and textural evidence showing that pseudomorphic Mtc-II resulted from an in-situ reaction between olivine and the carbonate component of the kimberlite melt in the decarbonation reactio. This reaction is supported by the preservation of abundant primary inclusions of periclase and to a lesser extent Fe-Mg-oxides in monticellite, perovskite and Mg-magnetite. Based on the preservation of primary periclase inclusions, we infer that periclase also existed in the groundmass, but was subsequently altered to brucite. We suggest that CO2 degassing in the latter stages of kimberlite emplacement into the crust is largely driven by the observed reaction between olivine and the carbonate melt. For this reaction to proceed, CO2 should be removed (i.e. degassed), which will cause further reaction and additional degassing in response to this chemical system change (Le Chatelier's principle). Our study demonstrates that these proposed decarbonation reactions may be a commonly overlooked process in the crystallisation of monticellite and exsolution of CO2, which may in turn contribute to the explosive eruption and brecciation processes that occur during kimberlite magma emplacement and pipe formation.
International Engineering Journal, Ouro Preto *** IN: PORT, Vol. 71, 1, pp. 27-35.
South America, Brazil
deposit - Chapada
Abstract: The Chapada Diamantina, located in the central region of the State of Bahia, is of important historical significance due to its diamond occurrences. Discovered in the nineteenth century, comprehensive research about the regional diamonds and their origins are still limited, demanding more investigation in the matter. Looking for insights about their genesis, mineral inclusions in 23 alluvial diamonds from 4 garimpos located in the Chapada Diamantina were analyzed through the use of Raman micro spectroscopy. Additionally, the characteristics of nitrogen aggregation of the host diamonds were measured using Fourier-transform infrared spectroscopy (FTIR). The diamonds from Chapada Diamantina consist mainly of well-formed crystals, with dominant dodecahedral habits, characterized by faint to very light yellow body colors, typically with green and brown radiation spots on their surface. The main surface textures observed are related to processes that took place in the late stage resorption and during the residence of the diamonds in placer environments. The diamonds are predominantly type IaAB, with a significant occurrence of poorly aggregated nitrogen (Type IaA diamond). The main mineral assemblages of the studied peridotitic inclusions refer to a harzburgitic paragenesis.
Geochimica et Cosmochimica Acta, in press available, 46p.
Russia, Siberia
deposit - Obnazhennaya
Abstract: The Obnazhennaya kimberlite in the NE Siberian craton hosts a most unusual cratonic xenolith suite, with common rocks rich in pyroxenes and garnet, and no sheared peridotites. We report petrographic and chemical data for whole rocks (WR) and minerals of 20 spinel and garnet peridotites from Obnazhennaya with Re-depletion Os isotope ages of 1.8-2.9 Ga (Ionov et al., 2015a) as well as 2 pyroxenites. The garnet-bearing rocks equilibrated at 1.6-2.8 GPa and 710-1050°C. Some xenoliths contain vermicular spinel-pyroxene aggregates with REE patterns in clinopyroxene mimicking those of garnet. The peridotites show significant scatter of Mg# (0.888-0.924), Cr2O3 (0.2-1.4 wt.%) and high NiO (0.3-0.4 wt.%). None are pristine melting residues. Low-CaO-Al2O3 (?0.9 wt.%) dunites and harzburgites are melt-channel materials. Peridotites with low to moderate Al2O3 (0.4-1.8 wt.%) usually have CaO > Al2O3, and some have pockets of calcite texturally equilibrated with olivine and garnet. Such carbonates, exceptional in mantle xenoliths and reported here for the first time for the Siberian mantle, provide direct evidence for modal makeover and Ca and LREE enrichments by ephemeral carbonate-rich melts. Peridotites rich in CaO and Al2O3 (2.7-8.0 wt.%) formed by reaction with silicate melts. We infer that the mantle lithosphere beneath Obnazhennaya, initially formed in the Mesoarchean, has been profoundly modified. Pervasive inter-granular percolation of highly mobile and reactive carbonate-rich liquids may have reduced the strength of the mantle lithosphere leading the way for reworking by silicate melts. The latest events before the kimberlite eruption were the formation of the carbonate-phlogopite pockets, fine-grained pyroxenite veins and spinel-pyroxene symplectites. The reworked lithospheric sections are preserved at Obnazhennaya, but similar processes could erode lithospheric roots in the SE Siberian craton (Tok) and the North China craton, where ancient melting residues and reworked garnet-bearing peridotites are absent.The modal, chemical and Os-isotope compositions of the Obnazhennaya xenoliths produced by reaction of refractory peridotites with melts are very particular (high Ca/Al, no Mg#-Al correlations, highly variable Cr, low 187Os/188Os, continuous modal range from olivine-rich to low-olivine peridotites, wehrlites and websterites) and distinct from those of fertile lherzolites in off-craton xenoliths and peridotite massifs. These features argue against the concept of ‘refertilization’ of cratonic and other refractory peridotites by mantle-derived melts as a major mechanism to form fertile to moderately depleted lherzolites in continental lithosphere. The Obnazhennaya xenoliths represent a natural rock series produced by ‘refertilization’, but include no rocks equivalent in modal, major and trace element to the fertile lherzolites. This study shows that ‘refertilization’ yields broad, continuous ranges of modal and chemical compositions with common wehrlites and websterites that are rare among off-craton xenoliths.
Abstract: The contents of radioactive elements and the uranium isotopic composition of kimberlite in the Arkhangelskaya pipe at the M.V. Lomonosov deposit and of nearby country rocks have been studied. A surplus of 234U isotope has been established in rocks from the near-pipe space. The high ? = 234U/238U ratio is controlled by the geological structure of the near-pipe space. A nonequilibrium uranium halo reaches two pipe diameters in size and can be regarded as a local ore guide for kimberlite discovery. The rocks in the nearpipe space are also characterized by elevated or anomalous U, Th, and K contents with respect to the background.
Abstract: The Bayan Obo ore deposit in Inner Mongolia, North China, the largest-known rare earth element (REE) deposit in the world, is closely associated with carbonatite dykes. Scarce zircon grains, with a wide range of ages and diverse origins, have been extracted from the Wu dyke, a REE-enriched calcitic carbonatite dyke 2?km from the East Ore Body of the Bayan Obo deposit. Three zircon populations were identified based on ages and trace element compositions: 1) Captured zircons with Paleoproterozoic and Archean ages. These zircons have REE patterns and moderate Th/U ratios similar to zircon with silicate inclusions from basement igneous rocks, which have been recognized as contaminants from wall rocks. 2) Carbonatite magmatic zircons with Mesoproterozoic ages. These zircons have high to extremely high Th/U ratios (13-1600), a characteristic signature of the Bayan Obo deposit. Two zircon grains yielded concordant 206Pb/238U ages (1.27?±?0.11?Ga???1.42?±?0.18?Ga) and 208Pb/232Th age (1.26?±?0.20?Ga) with calcite inclusions, indicating that the Wu dyke was emplaced at ca. 1.34?Ga, which coincides with a worldwide generation of Mesoproterozoic kimberlites, lamprophyres, carbonatites, and anorogenic magmatism. 3) Hydrothermal zircons with Caledonian and Triassic ages. The Caledonian zircon has 206Pb/238U age of 381?±?4?Ma and 208Pb/232Th age of 367?±?14?Ma with dolomite inclusion. These evidences are consistent with multiple stages of mineralization, Mesoproterozoic calcite carbonatite magmatism interacted by protracted fluxing of subduction-released Caledonian fluids during the closure of the Palaeo-Asian Ocean, coupled with interaction with the mantle wedge and metasomatism of overlying sedimentary carbonate.
Geochemistry International, Vol. 55, 12, pp. 1118-1130.
Russia
deposit - Lomonosov
Abstract: Thermodynamic numerical simulations were carried out to determine the principal simple and complex migration species of Ca, Mg, Na, K, Al, B, Mn, Mo, Sr, and U with Cl-, OH-, SO4?2, HCO3?, and CO32? in waters at the Lomonosov diamond deposit and to estimate the saturation indexes with respect to kaolinite, Na- and Mg-montmorillonite, Mg- and Na-saponite, muscovite and paragonite, biotite, phlogopite, chromite, pyrite, plagioclase (anorthite, labradorite, and andesine), olivine (forsterite and fayalite), diopside, pyrope, gypsum, anhydrite, barite, magnesite, calcite, dolomite, talc, chrysotile, chlorite, goethite, quartz, microcline, and albite. The waters are proved not to be saturated with respect to the primary (hydrothermal) minerals. The saturation of certain water samples with uranophane suggests that this mineral is of secondary genesis. The ascent of highly mineralized deep waters shall result in the dissolution of minerals whose concentrations are near the saturation ones. To maintain the ecological standards of the discharged waters, they should be diluted and/or purified by adsorbing dissolved U on a reducing reactive barrier.
Abstract: The varied lithologic facies and mineralogy resulting from emplacement of syngenetic alkaline, ultramafic and carbonatite (AUC) intrusions are made more diverse by variable weathering and alteration. Ultramafic-carbonatite intrusive complexes are a source for many valuable minerals including diamonds and rare earth element minerals. The intrusive bodies are often difficult to detect in the field due to their paucity, weathering, vegetation, and, in some instances, similarity to country rock, especially in the case of carbonatites among sedimentary carbonates. Remote spectroscopic detection is used extensively for geologic mapping yet has not been applied to differentiating sedimentary and igneous carbonate weathering profiles. Here we document the alteration mineralogy of a newly authenticated melilitite-clan carbonatite occurrence in the Avon Volcanic District in southeast Missouri, USA. The presence of lizardite, vermiculite, phlogopite, and andradite in the weathered crust of calcic and dolomitic carbonatites differentiate them from sedimentary dolomites. We apply field and laboratory spectral measurements to determine the feasibility of humid region AUC remote sensing and classification. Automated humid region detection and classification of carbonatites among sedimentary carbonates is shown to be possible using ratios of absorption features in the 2000-2400?nm range as well as features centered near 680, 900, and 1100?nm due transition metal charge transfer and crystal field splitting in garnet, sheet-silicates, and spinel.
Abstract: A comprehensive, internally consistent U-Pb and Lu-Hf isotope data set for 93 mantle-derived zircons from the Yakutian kimberlite province confirms and further refines the four major episodes of kimberlite magmatism on the Siberian craton: 421-409?Ma (Late Silurian-Early Devonian), 358-353?Ma (Late Devonian-Early Carboniferous), 226-218?Ma (Late Triassic), and 161-144?Ma (Middle-Late Jurassic). The relatively narrow, constant range of ?Hf values between +2 and +10 for both the Paleozoic and Mesozoic mantle-derived zircons (and by inference kimberlites) suggests that the volatile-rich magmas were repeatedly sourced from the convecting upper mantle beneath the Siberian craton. This finding is in keeping with the narrow and constant range of ?Nd values for groundmass perovskites from the Yakutian kimberlite province between +1.8 and +5.5 between 420 and 150?Ma. Our preferred model implies that the convecting upper mantle beneath the Yakutian kimberlite province ‘recovered’ rapidly back to ambient conditions shortly after the giant plume-related flood volcanic event that produced the Siberian Traps at 250?Ma. Although close spatial relationships exist between kimberlites and flood basalts on the Siberian craton during both the Paleozoic and Mesozoic, exact timing of the igneous events and the isotopic compositions of the diverse deep-sourced melting products rule out any direct genetic links.Besides the highly economic kimberlite-hosted diamond deposits of Late Devonian age (e.g., Mir and Udachnaya), the Siberian craton also contains significant Mesozoic placer diamond deposits (e.g., along the Anabar river), for which lamproite sources have been suggested recently. Our study shows that mantle-derived zircon megacryst fragments from the Ebelyakh placer deposit have Late Triassic ages of ca. 224?Ma. Their long-term depleted Hf isotopic compositions (+8.5 ?Hf) suggest that the alluvial diamonds were sourced from asthenosphere-derived Triassic kimberlites rather than from lithospheric mantle derived isotopically enriched lamproites.
Abstract: A comprehensive, internally consistent U-Pb and Lu-Hf isotope data set for 93 mantle-derived zircons from the Yakutian kimberlite province confirms and further refines the four major episodes of kimberlite magmatism on the Siberian craton: 421-409?Ma (Late Silurian-Early Devonian), 358-353?Ma (Late Devonian-Early Carboniferous), 226-218?Ma (Late Triassic), and 161-144?Ma (Middle-Late Jurassic). The relatively narrow, constant range of ?Hf values between +2 and +10 for both the Paleozoic and Mesozoic mantle-derived zircons (and by inference kimberlites) suggests that the volatile-rich magmas were repeatedly sourced from the convecting upper mantle beneath the Siberian craton. This finding is in keeping with the narrow and constant range of ?Nd values for groundmass perovskites from the Yakutian kimberlite province between +1.8 and +5.5 between 420 and 150?Ma. Our preferred model implies that the convecting upper mantle beneath the Yakutian kimberlite province ‘recovered’ rapidly back to ambient conditions shortly after the giant plume-related flood volcanic event that produced the Siberian Traps at 250?Ma. Although close spatial relationships exist between kimberlites and flood basalts on the Siberian craton during both the Paleozoic and Mesozoic, exact timing of the igneous events and the isotopic compositions of the diverse deep-sourced melting products rule out any direct genetic links.Besides the highly economic kimberlite-hosted diamond deposits of Late Devonian age (e.g., Mir and Udachnaya), the Siberian craton also contains significant Mesozoic placer diamond deposits (e.g., along the Anabar river), for which lamproite sources have been suggested recently. Our study shows that mantle-derived zircon megacryst fragments from the Ebelyakh placer deposit have Late Triassic ages of ca. 224?Ma. Their long-term depleted Hf isotopic compositions (+8.5 ?Hf) suggest that the alluvial diamonds were sourced from asthenosphere-derived Triassic kimberlites rather than from lithospheric mantle derived isotopically enriched lamproites.
Doklady Earth Sciences, Vol. 477, 2, pp. 1458-1460.
Russia
deposit - Nyturba
Abstract: Study of the magmatics in the Nakyn kimberlite field, with consideration of the isotope dating results, allowed us to establish a sequence of their formation. First, 368.5-374.4 Ma ago intrusions of the Vilyui-Markha dike belt formed. Then (363-364 Ma) intrusion of kimberlites took place. In the Early Carboniferous (338.2-345.6 Ma), alkaline basaltic magma intruded through faults controlling the kimberlites. The magmatic activity finished 331-324.9 Ma ago with the formation of explosive breccias. It has been found that the Nyurba kimberlite pipe consists of two bodies: their kimberlite melts have successively intruded through independent channels.
Journal of Appled Mathematics and Mechanics, Vol. 81, pp. 206-213.
Russia
deposit - Mir
Abstract: A linear analysis of the stability of the course of serpentization, that is, of the exothermic hydration reaction, due to the flow of water in a kimberlite pipe is carried out, taking both the heat conduction and the convective heat transfer by the fluid saturating the pipe rocks into account. It is shown that two different serpentization processes exist: a homogeneous process and an inhomogeneous process associated with a loss of stability by the homogeneous process and a non-uniform reaction rate distribution. Dimensionless similarity parameters that determine the course of the reaction are proposed. It is shown that convective heat transfer promotes a stabilization of the flow and the formation of a homogeneous serpentinite distribution. Other conditions being equal, an increase in the convective heat flux leads to an increase in the wavelengths of the unstable perturbations and to a decrease in their amplitude. A critical value of the flow rate exists, and, when this is exceeded, instability does not develop and serpentinization takes place under homogeneous conditions.
Abstract: MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) xenoliths are transported from the deep-cratonic lithosphere to the Earth's surface by Cretaceous kimberlites emplaced in the Kimberley area of the Kaapvaal Craton. MARID xenoliths have high modal abundances (70-80?vol%) of mica and amphibole, indicating their origin from a hydrous source. The ?18O values (4.7????18O???6.9‰) of phlogopite micas from 14 MARID samples indicate that these minerals are both 18O-enriched and 18O-depleted with respect to the average upper mantle ?18O value of 5.8?±?0.6‰. The range of ?2H values of phlogopites (?83????2H????53‰, n?=?14) of MARID xenoliths are slightly larger than the average mantle ?2H value (?70?±?10‰). The oxygen (?18Ophlogopites-amphibole?=??0.4 and 0.4‰) and hydrogen (?2Hphlogopite-amphibole?=?14 and 36‰) isotopic disequilibrium recorded from two MARID xenoliths suggests the duration of the last isotopic exchange, possibly just before the kimberlite emplacement, between these minerals and metasomatic fluids was too short to reach isotopic equilibrium. Our model calculation indicates that the phlogopites of MARID xenoliths underwent isotopic exchange with fluids of ?18O?=?5.5 to 10‰, ?2H?=??62 to ?90‰. The range of ?18O value of the calculated metasomatic fluids resembles the oxygen isotopic composition of the primary mantle carbonate (~ 6-9‰) suggesting interaction between carbonatic melt and MARID xenoliths in the continental lithospheric mantle. Furthermore, ?18O values of phlogopites together with previously published nitrogen isotope data (?11 ? ?15N ? 9‰; Banerjee et al., 2015) indicates incorporation of inhomogeneously distributed recycled crustal material from subducted crust within their source magma. Therefore, O-H-N isotope data for MARID xenoliths indicates their crystallization from geochemically heterogeneous magma in the upper continental mantle and subsequent metasomatism with mantle fluids.
Anais da Academia Brasileira de Ciencas, Vol. 78, 2, pp. 309-315.
Africa, Angola
deposit - Camafuca
Abstract: This work presents a geochemical study of a set of garnets, selected by their colors, from the Camafuca-Camazambo kimberlite, located on northeast Angola. Mantle-derived garnets were classified according to the scheme proposed by Grütter et al. (2004) and belong to the G1, G4, G9 and G10 groups. Both sub-calcic (G10) and Ca-saturated (G9) garnets, typical, respectively, of harzburgites and lherzolites, were identified. The solubility limit of knorringite molecule in G10D garnets suggests they have crystallized at a minimum pressure of about 40 to 45 kbar (4-4.5 GPa). The occurrence of diamond stability field garnets (G10D) is a clear indicator of the potential of this kimberlite for diamond. The chemistry of the garnets suggests that the source for the kimberlite was a lherzolite that has suffered a partial melting that formed basaltic magma, leaving a harzburgite as a residue.
Geological Survey of Western Australia, Report 182, 297p.
Australia
deposit - Ellendale area
Abstract: In 2005, Frogtech Geoscience completed OZ SEEBASE - a continental-scale depth-to-basement grid which shows the distribution of Phanerozoic basins across Australia. OZ SEEBASE is an open-file study that has been downloaded 1000s of times by industry, government and academia. This was followed in 2006 by the Proterozoic OZ SEEBASE interpretation including the main Proterozoic basins of Australia. The 2005 and 2006 OZ SEEBASE incorporated results from the Canning Basin Project completed by SRK Consulting for Shell during 1998-99.
Abstract: Establishing relationships between the long-term landscape evolution of drainage basins and the fill of sedimentary basins benefits from analysis of bedrock river terrace deposits. These fragmented detrital archives help to constrain changes in river system character and provenance during sediment transfer from continents (source) to oceans (sink). Thick diamondiferous gravel terrace deposits along the lower Orange River, southern Namibia, provide a rare opportunity to investigate controls on the incision history of a continental-scale bedrock river. Clast assemblage and heavy mineral data from seven localities permit detailed characterisation of the lower Orange River gravel terrace deposits. Two distinct fining-upward gravel terrace deposits are recognised, primarily based on mapped stratigraphic relationships (cross-cutting relationships) and strath and terrace top elevations, and secondarily on the proportion of exotic clasts, referred to as Proto Orange River deposits and Meso Orange River deposits. The older early to middle Miocene Proto Orange River gravels are thick (up to 50 m) and characterised by a dominance of Karoo Supergroup shale and sandstone clasts, whereas the younger Plio-Pleistocene Meso Orange River gravels (6-23 m thick) are characterised by more banded iron formation clasts. Mapping of the downstepping terraces indicates that the Proto gravels were deposited by a higher sinuosity river, and are strongly discordant to the modern Orange River course, whereas the Meso deposits were deposited by a lower sinuosity river. The heavy minerals present in both units comprise magnetite, garnet, amphibole, epidote and ilmenite, with rare titanite and zircon grains. The concentration of amphibole-epidote in the heavy minerals fraction increases from the Proto to the Meso deposits. The decrease in incision depths, recorded by deposit thicknesses above strath terraces, and the differences in clast character (size and roundness) and type between the two units, are ascribed to a more powerful river system during Proto-Orange River time, rather than reworking of older deposits, changes in provenance or climatic variations. In addition, from Proto- to Meso-Orange River times there was an increase in the proportion of sediments supplied from local bedrock sources, including amphibole-epidote in the heavy mineral assemblages derived from the Namaqua Metamorphic Complex. This integrated study demonstrates that clast assemblages are not a proxy for the character of the matrix, and vice versa, because they are influenced by the interplay of different controls. Therefore, an integrated approach is needed to improve prediction of placer mineral deposits in river gravels, and their distribution in coeval deposits downstream.
Abstract: The compositions of kimberlite melts at depth and upon emplacement in the upper crust remain elusive. This can be attributed to the unquantified effects of multiple processes, such as alteration, assimilation, xenocryst contamination, and fractional crystallisation. The inability to accurately constrain the composition and physical properties of kimberlite melts prevents a comprehensive understanding of their petrogenesis. To improve constraints on the compositions of kimberlite melts, we have combined modal analysis including the discrimination of xenocrystic from magmatic phases, with mineral chemistry determinations to reconstruct a whole-rock composition. We apply this approach to a sample of “fresh” macrocrystic hypabyssal kimberlite (sample BK-1) from the Bultfontein mine (Kimberley, South Africa). The accuracy of this whole-rock reconstruction method is validated by the similarity between reconstructed and measured whole-rock compositions. A series of corrections are then applied to account for the effects of post-emplacement serpentinisation, pre-emplacement olivine crystallisation, and the inclusion and assimilation of mantle material. This approach permits discernment of melt compositions at different stages of kimberlite evolution. The primitive melt parental to the Bultfontein kimberlite is estimated to contain 17.4-19.0?wt% SiO2, 20.2-22.8?wt% MgO, 20.9-21.9?wt% CaO, 2.1-2.3?wt% P2O5, 1.2-1.4?wt% TiO2, 0.9-1.1?wt% Al2O3, and 0.6-0.7?wt% K2O, and has a Mg# of 83.4-84.4. Primary volatile contents (i.e., after an attempt to account for volatile loss) are tentatively estimated at ~2.1-2.2?wt% H2O and ~22.9-25.4?wt% CO2. This composition is deficient in SiO2, MgO and H2O, but enriched in CaO and CO2 compared with most previous estimates of primitive kimberlite melts. We suggest that the primitive melt parental to the Bultfontein kimberlite was a transitional silicate-carbonate melt, which was progressively enriched in SiO2, MgO, Al2O3, Cr2O3, and Na2O through the assimilation of lithospheric mantle material. Comparisons with experimentally produced low-degree melts of carbonated lherzolite indicate that the Bultfontein kimberlite could have formed by ~0.5% melting of asthenospheric mantle at ~6.0-8.6?GPa (i.e., ~190-285?km) and ~1400-1500?°C. The low calculated Na2O contents (<0.2?wt%), which are inconsistent with derivation from low-degree melting of lherzolite, suggest that an alkali-bearing, volatile-rich fluid was exsolved during ascent or released after emplacement, and subsequently removed.
Abstract: The article reports basic design parameters of open pit mines of ALROSA, as well as criteria and factors that govern the choice of production capacity of an open pit diamond mine under conditions of permafrost. The analytical relations and tables to calculate open pit mine life are presented, and the influence of the rate of the downward advance of an open pit mine on its capacity is demonstrated. The authors formulate key provisions for a paragraph of the national standard of RF enabling systematization of approaches to optimization of open diamond mining parameters.
Abstract: The authors propose methods and means to monitor deformation and subsidence of ore crown under mining of open-pit bottom reserves by room-and-pillar system with cemented backfill in Mir Mine, ALROSA. The article describes layout and data of geomechanical monitoring. The mechanism of ore subsidence at the lower boundary of the safety pillar is determined.
Abstract: Pyrope-almandine garnets (Mg# = 28.3-44.9, Ca# = 15.5-21.3) from a heavy mineral concentrate of diamondiferous kimberlites of the largest diamond deposit, the Yubileinaya pipe, along with kimberlite- like rocks and diamondiferous volcano-sediments of the Laptev Sea coast, have been found to contain polymineral, predominantly acicular inclusions, composed of aggregates of shrilankite (Ti2ZrO6), rutile, ilmenite, clinopyroxene, and apatite. The presence of shrilankite as an inclusion in garnets from assumed garnet-pyroxene rocks of the lower crust, lifted up by diamond-bearing kimberlite, allows it to be considered as an indicator mineral of kimberlite, which expands the possibilities when searching for kimberlite in the Arctic.
Journal of Mining Science, Vol. 53, 1, pp. 126-132.
Russia
deposit - Mir
Abstract: The structural and chemical surface transformation of basic kimberlite-forming minerals (calcite, olivine, serpentine) under the contact with natural and waste mineralized water and products of electrochemical treatment of the water are studied using X-ray photoelectronic spectroscopy, scanning electron microscopy and X-ray spectral micro-analysis, and atomic force microscopy. It is found that contact with kimberlite extract and recycling water induces chemical modification of calcite surface, which consists in adsorption of hydrocarbon impurities, and chlorine- and silica-bearing compounds, majority of which are removed during interaction with the product of electrochemical treatment of recycling water. The change in the structural and chemical surface properties of rock-forming silicates, aside from adsorption-desorption of organic compound, is also connected with the distortion of nano-size layer structure after leaching of Mg, Fe and Si, and with the carbonatization of the surface.
Society of Exploration Geophysicists, Interpretation, August T 299, 13p.
Canada, Northwest Territories
deposit - Tli Kwi Cho
Abstract: The Tli Kwi Cho (TKC) kimberlite complex contains two pipes, called DO-27 and DO-18, which were discovered during the Canadian diamond exploration rush in the 1990s. The complex has been used as a testbed for ground and airborne geophysics, and an abundance of data currently exist over the area. We have evaluated the historical and geologic background of the complex, the physical properties of interest for kimberlite exploration, and the geophysical surveys. We have carried out 3D inversion and joint interpretation of the potential field data. The magnetic data indicate high susceptibility at DO-18, and the magnetic inversion maps the horizontal extent of the pipe. DO-27 is more complicated. The northern part is highly magnetic and is contaminated with remanent magnetization; other parts of DO-27 have a low susceptibility. Low densities, obtained from the gravity and gravity gradiometry data, map the horizontal extents of DO-27 and DO-18. We combine the 3D density contrast and susceptibility models into a single geologic model that identifies three distinct kimberlite rock units that agree with drilling data. In further research, our density and magnetic susceptibility models are combined with information from electromagnetic data to provide a multigeophysical interpretation of the TKC kimberlite complex.
Abstract: A comprehensive petrographic and in situ major and trace element study of rutile, ilmenite and Ti-magnetite was undertaken in six lower crustal xenoliths of metabasaltic (?underplate) and metasedimentary (subduction) origin from the Diavik kimberlites (central Slave Craton, Canada). The aims of the study were to improve our understanding of trace element incorporation into these Ti-minerals, and to use these systematics to obtain insights into lower continental crust formation and evolution. Abundant (oxy)exsolution of titanomagnetite lamellae, blocky rutile, as well as minor pleonaste and zircon in ilmenite from metabasaltic granulites are proposed to reflect cooling from magmatic or metamorphic temperatures and subsequent secular mantle cooling. This explains the large spread in Zr-in-rutile temperatures (>200°C) and may partly be responsible for the substantial heterogeneity of other trace element concentrations in rutile and ilmenite. Even after accounting for trace element heterogeneity and modal uncertainties, mass-balance calculations indicate that both Ti and Nb in lower crustal granulites are largely controlled by rutile and ilmenite. Rutile U-Pb data define discordia arrays that yield upper intercept ages broadly coincident with the 1•27 Ga giant Mackenzie dike swarm event, suggesting reheating of the lower crust above the rutile U-Pb closure temperature, whereas lower intercept ages roughly correspond to the age of Cretaceous to Eocene kimberlite magmatism. Subsequent cooling led to partial resetting and data spread along the concordia. Closer inspection reveals that inter-grain concentrations of elements that are compatible in rutile (Nb, Ta, W, U), but highly incompatible in the abundant silicate minerals (in equilibrium with melt), are heterogeneous and contrast with the more homogeneous concentrations of the transition metals (NiO, V). This may indicate that local reaction partners for diffusive homogenization of these element concentrations were absent. Nb/Ta is also highly variable at the sample scale. This may be explained by prograde growth from high-Nb/Ta mineral precursors (e.g. biotite) in the metasedimentary granulites and crystallization of the protoliths to the metabasaltic granulites from a mafic magma that had experienced fractionation of ilmenite with low Nb/Ta in a crustal magma chamber. Thus, (Fe)-Ti minerals represent high field strength element ‘islands’ in the granulite silicate matrix. The lack of homogenization and persistence of high-energy grain boundaries, such as exsolution lamellae, further indicate that the lower continental crust remained essentially dry and did not recrystallize, possibly since Neoarchaean metamorphism.
Society of Exploration Geophysicists, Interpretation, August T 313, 13p.
Canada, Northwest Territories
deposit - Tli Kwi Cho
Abstract: We focus on the task of finding a 3D conductivity structure for the DO-18 and DO-27 kimberlites, historically known as the Tli Kwi Cho (TKC) kimberlite complex in the Northwest Territories, Canada. Two airborne electromagnetic (EM) surveys are analyzed: a frequency-domain DIGHEM and a time-domain VTEM survey. Airborne time-domain data at TKC are particularly challenging because of the negative values that exist even at the earliest time channels. Heretofore, such data have not been inverted in three dimensions. In our analysis, we start by inverting frequency-domain data and positive VTEM data with a laterally constrained 1D inversion. This is important for assessing the noise levels associated with the data and for estimating the general conductivity structure. The analysis is then extended to a 3D inversion with our most recent optimized and parallelized inversion codes. We first address the issue about whether the conductivity anomaly is due to a shallow flat-lying conductor (associated with the lake bottom) or a vertical conductive pipe; we conclude that it is the latter. Both data sets are then cooperatively inverted to obtain a consistent 3D conductivity model for TKC that can be used for geologic interpretation. The conductivity model is then jointly interpreted with the density and magnetic susceptibility models from a previous paper. The addition of conductivity enriches the interpretation made with the potential fields in characterizing several distinct petrophysical kimberlite units. The final conductivity model also helps better define the lateral extent and upper boundary of the kimberlite pipes. This conductivity model is a crucial component of the follow-up paper in which our colleagues invert the airborne EM data to recover the time-dependent chargeability that further advances our geologic interpretation.
South African Journal of Geology, Vol. 120, 1, pp. 1-20.
Africa, South Africa
deposit - Jagersfontein
Abstract: Our earlier studies continued in a diligent search for rare ultradeep xenoliths in the kimberlite diatreme at Jagersfontein. The search has met with moderate success insofar as 20 majorite-bearing (decomposed to *gt + lamellar px) xenoliths are identified. Discrete gts (1 to 2 cm), gt-rich layers (2 to 3 cm) in lherzolites, and rare megacrystic gts (>3 cm) from xenoliths characterize the ultradeep suite. Pyroxene lamellae are crystallographically controlled along {111} gt planes, but px may also be prismatic, lensoidal, coarsely graphic, or annular to gt; jigsaw, rather than 120° dihedral textures, are typical. Gt ranges from Pyr68-74 mole% and CaO - Cr2O3 relations, with two exceptions, are distinctly lherzolitic. Cpx = Wo37-46 mole%, Jd3-19 mole%, with 0.4 to 2.4 wt% Cr2O3; opx = 92 to 95 mole% en, and ol averages 92.5 mole% with maximum wt% 0.1 CaO, 0.4 NiO, and 0.1 Cr2O3. A new class of 10 ultradeep xenoliths has lamellar spinel (Cr/Cr + Al = 0.74; Mg/Mg + Fe = 0.58) in addition to cpx with gt >3wt% Cr2O3 (c.f. 0.5 to 1.5 for sp-free types). Five samples are texturally linked but are compositional outliers to the central body of data: two are sp hosts (Cr# 0.69, Mg# 0.76) and (Cr# 0.74, Mg# 0.57) to gt (Pyr72) + cpx (Jd14); one is a gt megacryst (Pyr80) with sp (Cr# 57, Mg# 69); and the remaining two are unusually rich in chromium with gt = 7.3 to 8.2 wt% Cr2O3, rimmed by cpx (2.3 to 3-3 wt% Cr2O3). In addition, there are 17 xenoliths with compositional affinities to the ultradeep suite but lacking the texturally diagnostic lamellar intergrowths of cpx in gt are possibly completely equilibrated to gt + irregular cpx. Results from the new collection substantiate our earlier conclusions that the mantle was sampled by thejagersfontein kimberlite from the lower lithosphere (250 to 350 km) and the transition zone (435 km) with diagnostic high P-T majorite in lherzolite that decomposed to gt + px at one or more interruptive stations (e.g. lithosphere-asthenosphere boundary), and at one or another time, en route to the surface. Homogeneous majorite occurs as diamond inclusions at Jagersfontein but these are eclogitic, leading to the proposition that the source region in the asthenosphere was an unassimilated mixture of lherzolite and eclogite in the Mid-Cretaceous at the time of kimberlite sampling. Important questions arise: Is majorite primordial; did majorite form exclusively from the transition of pyroxene; or did subsequent dissolution into coexisting garnet take place? Why has majorite not been identified in eclogite, nor diamonds of lherzolitic affinity? Does the formation of majorite and the crystallization of encapsulating diamond imply distinct high P-T events?
Society of Exploration Geophysicists, Interpretation, August T 327, 14p.
Canada, Northwest Territories
deposit -Tli Kwi Cho
Abstract: The geologically distinct DO-27 and DO-18 kimberlites, often called the Tli Kwi Cho (TKC) kimberlites, have been used as a testbed for airborne geophysical methods applied to kimberlite exploration. This paper, which is the last of a three-part series, focuses on extracting chargeability information from time-domain electromagnetic (TEM) data. Three different TEM surveys, having similar coincident-loop geometry, have been carried out over TKC. Each records negative transients over the main kimberlite units and this is a signature of induced polarization (IP) effects. By applying a TEM-IP inversion workflow to a VTEM data set we decouple the EM and IP responses in the observations and then recover 3D pseudo-chargeability models at multiple times. A subsequent analysis is used to recover Cole-Cole parameters. Our models demonstrate that both DO-18 and DO-27 pipes are chargeable, but they have different Cole-Cole time constants: 110 and 1160 ?s, respectively. At DO-27, we also distinguish between two adjacent kimberlite units based on their respective Cole-Cole time constants. Our chargeability models are combined with the den-sity, magnetic susceptibility and conductivity models from Papers I and II and allow us to build a 3D petrophysical model of TKC using only information obtained from airborne geophysics. Comparison of this final petrophysical model to a 3D geological model derived from the extensive drilling program demonstrates that we can characterize the three main kimberlite units at TKC: HK, VK, and PK in 3D by using airborne geophysics.
Abstract: The mantle beneath the Cullinan kimberlite (formerly known as "Premier") is a unique occurrence of diamondiferous cratonic mantle where diamonds were generated contemporaneously and shortly following a mantle upwelling that led to the formation of a Large Igneous Province that produced the world's largest igneous intrusion - the 2056?Ma Bushveld Igneous Complex (BIC). We studied 332 diamond inclusions from 202 Cullinan diamonds to investigate mantle thermal effects imposed by the formation of the BIC. The overwhelming majority of diamonds come from three parageneses: (1) lithospheric eclogitic (69%), (2) lithospheric peridotitic (21%), and (3) sublithospheric mafic (9%). The lithospheric eclogitic paragenesis is represented by clinopyroxene, garnet, coesite and kyanite. Main minerals of the lithospheric peridotitic paragenesis are forsterite, enstatite, Cr-pyrope, Cr-augite and spinel; the sublithospheric mafic association includes majorite, CaSiO3 phases and omphacite. Diamond formation conditions were calculated using an Al-in-olivine thermometer, a garnet-clinopyroxene thermometer, as well as majorite and Raman barometers. The Cullinan diamonds may be unique on the global stage in recording a cold geotherm of 40?mW/m2 in cratonic lithosphere that was in contact with underlying convecting mantle at temperatures of 1450-1550?°C. The studied Cullinan diamonds contain a high proportion of inclusions equilibrated at temperatures exceeding the ambient 1327?°C adiabat, i.e. 54% of eclogitic diamonds and 41% of peridotitic diamonds. By contrast, ? 1% of peridotitic diamond inclusions globally yield equally high temperatures. We propose that the Cullinan diamond inclusions recorded transient, slow-dissipating thermal perturbations associated with the plume-related formation of the ~2?Ga Bushveld igneous province. The presence of inclusions in diamond from the mantle transition zone at 300-650?km supports this view. Cullinan xenoliths indicative of the thermal state of the cratonic lithosphere at ~1.2?Ga are equilibrated at the relatively low temperatures, not exceeding adiabatic. The ability of diamonds to record super-adiabatic temperatures may relate to their entrainment from the deeper, hotter parts of the upper mantle un-sampled by the kimberlite in the form of xenoliths or their equilibration in a younger lithosphere after a decay of the thermal disturbance.
Nestola, F., Korolev, N., Kopylova, M., Rotiroti, N., Pearson, D.G., Pamato, M.G., Alvaro, M., Peruzzo, L., Gurney, J.J., Moore, A.E., Davidson, J.
CaSiO3 perovskite in diamond indicates the recycling of oceanic crust into the lower mantle.
Nature, Vol. 555, March 8, pp. 237-241.
Mantle
deposit - Cullinan
Abstract: Laboratory experiments and seismology data have created a clear theoretical picture of the most abundant minerals that comprise the deeper parts of the Earth’s mantle. Discoveries of some of these minerals in ‘super-deep’ diamonds—formed between two hundred and about one thousand kilometres into the lower mantle—have confirmed part of this picture1,2,3,4,5. A notable exception is the high-pressure perovskite-structured polymorph of calcium silicate (CaSiO3). This mineral—expected to be the fourth most abundant in the Earth—has not previously been found in nature. Being the dominant host for calcium and, owing to its accommodating crystal structure, the major sink for heat-producing elements (potassium, uranium and thorium) in the transition zone and lower mantle, it is critical to establish its presence. Here we report the discovery of the perovskite-structured polymorph of CaSiO3 in a diamond from South African Cullinan kimberlite. The mineral is intergrown with about six per cent calcium titanate (CaTiO3). The titanium-rich composition of this inclusion indicates a bulk composition consistent with derivation from basaltic oceanic crust subducted to pressures equivalent to those present at the depths of the uppermost lower mantle. The relatively ‘heavy’ carbon isotopic composition of the surrounding diamond, together with the pristine high-pressure CaSiO3 structure, provides evidence for the recycling of oceanic crust and surficial carbon to lower-mantle depths.https://www.nature.com/articles/nature25972
Abstract: A wide number of genetic models have been proposed for volcanically transported ruby and sapphire deposits around the world. In this contribution we compare the trace element chemistry, mineral and melt inclusions, and oxygen isotope ratios in blue to reddish-violet sapphires from Yogo Gulch, Montana, U.S.A., with rubies from the Chantaburi-Trat region of Thailand and the Pailin region of Cambodia. The similarities between Thai/Cambodian rubies and Yogo sapphires suggest a common origin for gem corundum from both deposits. Specifically, we advance a model whereby sapphires and rubies formed through a peritectic melting reaction when the lamprophyre or basalts that transported the gem corundum to the surface partially melted Al-rich lower crustal rocks. Furthermore, we suggest the protolith of the rubies and sapphires was an anorthosite or, in the case of Thai/Cambodian rubies, an anorthosite subjected to higher pressures and converted into a garnet-clinopyroxenite. In this model the rubies and sapphires are rightfully considered to be xenocrysts in their host basalts or lamprophyre; however, in this scenario they are not "accidental" xenocrysts but their formation is intimately and directly linked to the magmas that transported them to the surface. The similarities in these gem corundum deposits suggests that the partial melting, non-accidental xenocryst model may be more wide-reaching and globally important than previously realized. Importantly, in both cases the gem corundum has an ostensibly "metamorphic" trace element signature, whereas the presence of silicate melt (or magma) inclusions shows they ought to be considered to be "magmatic" rubies and sapphires. This discrepancy suggests that existing trace element discriminant diagrams intended to separate "metamorphic" from "magmatic" gem corundum ought to be used with caution.
Abstract: Kimberlite pipes from Chidliak, Baffin Island, Nunavut, Canada host surface-derived Paleozoic carbonate xenoliths containing conodonts. Conodonts are phosphatic marine microfossils that experience progressive, cumulative and irreversible colour changes upon heating that are experimentally calibrated as a conodont colour alteration index (CAI). CAI values permit us to estimate the temperatures to which conodont-bearing rocks have been heated. Conodonts have been recovered from 118 samples from 89 carbonate xenoliths collected from 12 of the pipes and CAI values within individual carbonate xenoliths show four types of CAI distributions: (1) CAI values that are uniform throughout the xenolith; (2) lower CAIs in core of a xenolith than the rim; (3) CAIs that increase from one side of the xenolith to the other; and, (4) in one xenolith, higher CAIs in the xenolith core than at the rim. We have used thermal models for post-emplacement conductive cooling of kimberlite pipes and synchronous heating of conodont-bearing xenoliths to establish the temperature-time history of individual xenoliths within the kimberlite bodies. Model results suggest that the time-spans for xenoliths to reach the peak temperatures recorded by CAIs varies from hours for the smallest xenoliths to 2 or 3 years for the largest xenoliths. The thermal modelling shows the first three CAI patterns to be consistent with in situ conductive heating of the xenoliths coupled to the cooling host kimberlite. The fourth pattern remains an anomaly.
Abstract: The first results of study of minerals and diamonds of diamond-bearing eclogites from kimberlites of the Yubileinaya pipe with a variable percent amount of clinopyroxene and garnet are presented. Samples with a garnet content from 30 to 90% of the xenolith volume are dominant among the round to oval xenoliths with diamonds. Five eclogite samples contain grains of accessory rutile, as well as corundum and kyanite. Some samples host two or more diamond crystals.
Earth Planetary Science Letters, Vol. 490, pp. 77-87.
Canada, Ontario
deposit - Victor
Abstract: The central Superior Craton hosts both the diamondiferous 1.1 Ga Kyle Lake and Jurassic Attawapiskat kimberlites. A major thermal event related to the Midcontinent Rift at ca. 1.1 Ga induced an elevated geothermal gradient that largely destroyed an older generation of diamonds, raising the question of when, and how, the diamond inventory beneath Attawapiskat was formed. We determined Re-Os isotope systematics of sulphides included in diamonds from Victor by isotope dilution negative thermal ionisation mass spectrometry in order to obtain insights into the age and nature of the diamond source in the context of regional tectonothermal evolution. Regression of the peridotitic inclusion data (n = 14 of 16) yields a 718 ± 49 Ma age, with an initial 187Os/188Os ratio of 0.1177 ± 0.0016, i.e. depleted at the time of formation (?Os -3.7 ± 1.3). Consequently, Re depletion model ages calculated for these samples are systematically overestimated. Given that reported 187Os/188Os in olivine from Attawapiskat xenoliths varies strongly (0.1012-0.1821), the low and nearly identical initial Os of sulphide inclusions combined with their high 187Re/188Os (median 0.34) suggest metasomatic formation from a mixed source. This was likely facilitated by percolation of amounts of melt sufficient to homogenise Os, (re)crystallise sulphide and (co)precipitate diamond; that is, the sulphide inclusions and their diamond host are synchronous if not syngenetic. The ?720 Ma age corresponds to rifting beyond the northern craton margin during Rodinia break-up. This suggests mobilisation of volatiles (C, N, S) and Os due to attendant mantle stretching and metasomatism by initially oxidising and S-undersaturated melts, which ultimately produced lherzolitic diamonds with high N contents compared to older Kyle Lake diamonds. Thus, some rift-influenced settings are prospective with respect to diamond formation. They are also important sites of hidden, intra-lithospheric volatile redistribution that can be revealed by diamond studies. Later emplacement of the Attawapiskat kimberlites, linking the carbon cycle to the surface, was associated with renewed disturbance during passage of the Great Meteor Hotspot. Lherzolitic diamond formation from oxidising small-volume melts may be the expression of an early and deep stage of the lithospheric conditioning required for the successful eruption of kimberlites, which complements the late and shallow emplacement of volatile-rich metasomes after upward displacement of a redox freezing front.
Abstract: Identification of the primary compositions of mantle-derived melts is crucial for understanding mantle compositions and physical conditions of mantle melting. However, these melts rarely reach the Earth's surface unmodified because of contamination, crystal fractionation and degassing, processes that occur almost ubiquitously after melt generation. Here we report snapshots of the melts preserved in sheared peridotite xenoliths from the Udachnaya-East kimberlite pipe, in the central part of the Siberian craton. These xenoliths are among the deepest mantle samples and were delivered by kimberlite magma from 180-230?km depth interval, i.e. from the base of the cratonic lithosphere. The olivine grains of the sheared peridotites contain secondary inclusions of the crystallized melt with bulk molar (Na?+?K)/Ca?~?3.4. Various Na-K-Ca-, Na-Ca-, Na-Mg-, Ca-Mg- and Ca-carbonates, Na-Mg-carbonates with additional anions, alkali sulphates and halides are predominant among the daughter minerals in secondary melt inclusions, whereas silicates, oxides, sulphides and phosphates are subordinate. These inclusions can be considered as Cl-S-bearing alkali-carbonate melts. The presence of aragonite, a high-pressure polymorph of CaCO3, among the daughter minerals suggests a mantle origin for these melt inclusions. The secondary melt inclusions in olivine from the sheared peridotite xenoliths and the melt inclusions in phenocrystic olivines from the host kimberlites demonstrate similarities, in daughter minerals assemblages and trace-element compositions. Moreover, alkali-rich minerals (carbonates, halides, sulphates and sulphides) identified in the studied melt inclusions are also present in the groundmass of the host kimberlites. These data suggests a genetic link between melt enclosed in olivine from the sheared peridotites and melt parental to the Udachnaya-East kimberlites. We suggest that the melt inclusions in olivine from mantle xenoliths may represent near primary, kimberlite melts. These results are new evidence in support of the alkali?carbonate composition of kimberlite melts in their source regions, prior to the kimberlite emplacement into the crust, and are in stark contrast to the generally accepted ultramafic silicate nature of parental kimberlite liquids.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0567-y 9p.
Canada, Quebec
deposit - Renard
Abstract: The Renard 2 kimberlite pipe is one of nine diamondiferous kimberlite pipes that form a cluster in the south-eastern portion of the Superior Province, Québec, Canada and is presently being extracted at the Renard Mine. It is interpreted as a diatreme-zone kimberlite consisting of two Kimberley-type pyroclastic units and related country rock breccias, all cross-cut by coherent kimberlite dykes and irregular intrusives. Renard 2 has been the subject of numerous diamond drilling campaigns since its discovery in 2001. The first two geological models modelled kimberlite and country rock breccia units separately. A change in modelling philosophy in 2009, which incorporated the emplacement envelope and history, modelled the entire intrusive event and projected the pipe shape to depth allowing for more targeted deep drilling where kimberlite had not yet been discovered. This targeted 2009 drilling resulted in a?>?400% increase in the volume of the Indicated Resource. Modelling only the kimberlite units resulted in a significant underestimation of the pipe shape. Current open pit and underground mapping of the pipe shape corresponds well to the final 2015 geological model and contact changes observed are within the expected level of confidence for an Indicated Resource. This study demonstrates that a sound understanding of the geological emplacement is key to developing a reliable 3D geological and resource model that can be used for targeted delineation drilling, feasibility studies and during the initial stages of mining.
Journal of African Earth Sciences, Vol. 142, pp. 193-206.
Africa, Tanzania
deposit - Oldoinyo Lengai
Abstract: Oldoinyo Lengai, a stratovolcano in northern Tanzania, is most famous for being the only currently active carbonatite volcano on Earth. The bulk of the volcanic edifice is dominated by eruptive products produced by silica-undersaturated, peralkaline, silicate magmas (effusive, explosive and/or as cumulates at depth). The recent (2007-2008) explosive eruption produced the first ever recorded pyroclastic flows at this volcano and the accidental lithics incorporated into the pyroclastic flows represent a broad variety of different rock types, comprising both extrusive and intrusive varieties, in addition to various types of cumulates. This mix of different accidental lithics provides a unique insight into the inner workings of the world's only active carbonatite volcano. Here, we focus on the magnetic mineralogy and the rock magnetic properties of a wide selection of samples spanning the spectrum of Oldoinyo Lengai rock types compositionally, as well from a textural point of view. Here we show that the magnetic properties of most extrusive silicate rocks are dominated by magnetite-ulvöspinel solid solutions, and that pyrrhotite plays a larger role in the magnetic properties of the intrusive silicate rocks. The natrocarbonatitic lavas, for which the volcano is best known for, show distinctly different magnetic properties in comparison with the silicate rocks. This discrepancy may be explained by abundant alabandite crystals/blebs in the groundmass of the natrocarbonatitic lavas. A detailed combination of petrological/mineralogical studies with geophysical investigations is an absolute necessity in order to understand, and to better constrain, the overall architecture and inner workings of the subvolcanic plumbing system. The results presented here may also have implications for the quest in order to explain the genesis of the uniquely natrocarbonatitic magmas characteristic of Oldoinyo Lengai.
Bulletin of the Geological Survey of Finland, Vol. 79, 2, pp. 203-215.
Europe, Finland
deposit - Lentiira Kuhmo
Abstract: The Lentiira-Kuhmo-Kostomuksha triangle, along the Finland - Russian border and within the central part of the Archean Karelian craton, contains numerous examples of phlogopite-rich, ultramafic, mantle-xenocryst-bearing and, in some cases, diamond-bearing dike rocks. Laser probe Ar-Ar data on phlogopite from 3 dike rocks on the Finnish side (Lentiira, Kuhmo) all gave ages within error of each other, 1202 ± 3 Ma (2?), 1199 ± 3 Ma (2?) and 1204 ± 4 Ma (2?) while a fourth sample produced mixed ages. Published Rb-Sr dates on mineralogically and chemically similar dikes from the Russian side (Kostomuksha) are 1232 ± 5 Ma. The question remains open whether these represent two distinct age populations or whether differences in isotopic system behavior are the reason for the 30 m.y. age difference.
Bulletin of the Geological Survey of Finland, Vol. 73, 1-2, pp. 47-58.
Europe, Finland
deposit - Lahtojoki
Abstract: Eleven relatively large (diameter 1-2 mm) zircon grains extracted from the Lahtojoki kimberlite pipe (Eastern Finland Kimberlite Province) have been analysed by the ion microprobe NORDSIM for their U- and Pb- isotopic composition. The 207Pb/206Pb ages fall into two concordant age groups: 2.7 Ga and 1.8 Ga. Discordant ages between these two groups are believed to result from partial resetting of Archaean grains in the 1.8 Ga thermal event. Since other datingmethods imply that kimberlites emplaced c. 0.6 Ga ago it is clear that the analysed zircons are xenocrysts inherited from older sources and do not provide the age of the kimberlite magmatism. Their unusual size and morphology, together with very low U- and Pb-concentrations, suggest, however, that these zircon grains are not derived from typical Archaean gneisses. More likely, they originate from lower crustal mafic pegmatites and from hydrous coarse-grained veins within the uppermost lithospheric mantle. The predominance of 1.8 Ga old xenocrystic grains, together with the recovery of mafic granulite xenoliths of similar age in the kimberlites (Hölttä et al. 2000), emphasises the importance of post-collisional lower crustal growth and reworking in central Fennoscandia.
Periodico di Mineralogia, Vol. 86, pp. 213-228. pdf
India
deposit - Balkamthota Vanka
Abstract: Systematic closely spaced geological traverses conducted in the year 2010, in Lattavaram Kimberlite Cluster (LKC) of Anantapur district, Andhra Pradesh, India, have led to the discovery of a new kimberlite pipe outcrop in the river bed of Balkamthota Vanka (name of the stream used by local farmers) at its confluence with Penna River, close to Pennahobilam. This new pipe occurs at a distance of 1.5 km in NE direction to hitherto reported pipes-5 and 13 occurring at Muligiripalli and Tummatapalli respectively in the LKC of the Wajrakarur Kimberlite Field (WKF). With this pipe, the total number of kimberlite pipes in the WKF raises to 48, considering all the kimberlites discovered by various public and private organizations so far. Preliminary petrography, geochemistry, petrogenetic aspects and diamond prospectivity of the new occurrence have been presented here. Mineralogically, the kimberlite constitutes olivine macrocrysts, serpentinsed olivine psuedomorphs with xenocrystic ilmenite, phlogopite, perovskite, magnetite, Cr-diopside, garnet along with calcite veins. The kimberlite is classified as hypabyssal macrocrystic calcite- phlogopite kimberlite. Mineralogically, the new kimberlite pipe appears as archetypal Group- I kimberlite however, geochemically; the kimberlite shows character of both Group- I and II varieties, more close to lamproitic character. Although it is too early to comment, based on limited analyses carried out in this study, the diamond potentiality of this pipe is not encouraging; it is noteworthy that it highly warrants detailed investigations involving bulk rock geochemistry and drilling to assess its definite geochemical status, petrogenesis and diamond potentiality.
The P3 kimberlite and P4 lamproite, Wajrakur kimberlite field, India: mineralogy, and major and minor element compositions of olivines as records of their phenocrystic vs xenocrystic origin.
Abstract: The unique, giant, rare earth element (REE) deposit at Bayan Obo, northern China, is the world’s largest REE deposit. It is geologically complex, and its genesis is still debated. Here, we report in situ Th-Pb dating and Nd isotope ratios for monazite and Sr isotope ratios for dolomite and apatite from fresh drill cores. The measured monazite ages (361-913 Ma) and previously reported whole-rock Sm-Nd data show a linear relationship with the initial Nd isotope ratio, suggesting a single-stage evolution from a Sm-Nd source that was formed before 913 Ma. All monazites show consistent ?Nd(1.3Ga) values (0.3 ± 0.6) close to those of the adjacent 1.3 Ga carbonatite and mafic dikes. The primary dolomite and apatite show lower 87Sr/86Sr ratios (0.7024-0.7030) than the recrystallized dolomite (0.7038-0.7097). The REE ores at Bayan Obo are interpreted to have originally formed as products of ca. 1.3 Ga carbonatitic magmatism and to have undergone subsequent thermal perturbations induced by Sr-rich, but REE-poor, metamorphic fluids derived from nearby sedimentary rocks.
Earth Planetary Science Letters, Vol. 491, pp. 134-147.
Africa, South Africa
deposit - De Beers-Pool
Abstract: Fluid/melt inclusions in diamonds, which were encapsulated during a metasomatic event and over a short period of time, are isolated from their surrounding mantle, offering the opportunity to constrain changes in the sub-continental lithospheric mantle (SCLM) that occurred during individual thermo-chemical events, as well as the composition of the fluids involved and their sources. We have analyzed a suite of 8 microinclusion-bearing diamonds from the Group I De Beers Pool kimberlites, South Africa, using FTIR, EPMA and LA-ICP-MS. Seven of the diamonds trapped incompatible-element-enriched saline high density fluids (HDFs), carry peridotitic mineral microinclusions, and substitutional nitrogen almost exclusively in A-centers. This low-aggregation state of nitrogen indicates a short mantle residence times and/or low mantle ambient temperature for these diamonds. A short residence time is favored because, elevated thermal conditions prevailed in the South African lithosphere during and following the Karoo flood basalt volcanism at ?180 Ma, thus the saline metasomatism must have occurred close to the time of kimberlite eruptions at ?85 Ma. Another diamond encapsulated incompatible-element-enriched silicic HDFs and has 25% of its nitrogen content residing in B-centers, implying formation during an earlier and different metasomatic event that likely relates to the Karoo magmatism at ca. 180 Ma. Thermometry of mineral microinclusions in the diamonds carrying saline HDFs, based on Mg-Fe exchange between garnet-orthopyroxene (Opx)/clinopyroxene (Cpx)/olivine and the Opx-Cpx thermometer, yield temperatures between 875-1080?°C at 5 GPa. These temperatures overlap with conditions recorded by touching inclusion pairs in diamonds from the De Beers Pool kimberlites, which represent the mantle ambient conditions just before eruption, and are altogether lower by 150-250?°C compared to P-T gradients recorded by peridotite xenoliths from the same locality. Oxygen fugacity differs as well. The calculated for the saline HDF compositions (to ?1.34) are higher by about a log unit compared with that recorded by xenoliths at 4-7 GPa. We conclude that enriched saline HDFs mediated the metasomatism that preceded Group I kimberlite eruptions in the southwestern Kaapvaal craton, and that their ‘cold and oxidized’ nature reflects their derivation from a deep subducting slab. This event had little impact on the temperature and redox state of the Kaapvaal lithosphere as a reservoir, however, it likely affected its properties along limited metasomatized veins and their wall rock. To reconcile the temperature and oxygen fugacity discrepancy between inclusions in diamonds and xenoliths, we argue that xenoliths did not equilibrate during the last saline metasomatic event or kimberlite eruption. Thus the P-T-gradients they record express pre-existing lithospheric conditions that were likely established during the last major thermal event in the Kaapvaal craton (i.e. the Karoo magmatism at ca. 180 Ma).
Abstract: Using IR-Fourier spectrometry (FTIR) and simultaneous thermal analysis combined with quadrupole mass spectrometry of thermal decomposition products (STA + QMS), olivines and clinopyroxene from xenolites of spinel and garnet lherzolites contained in kimberlites and alkaline basalts were studied to confirm the occurrence of hydrogen and carbon within the structure of the minerals, as well as to specify the forms of H and C. The presence of hydroxyl ions (OH-) and molecules of crystal hydrate water (H2Ocryst) along with CO2, CH, CH2, and CH3 groups was detected, which remained within the structures of mantle minerals up to 1300°C (by the data of both techniques). The total water (OH-and H2Ocryst) was the prevailing component of the C-O-H system.
Mineralogy and Petrology, in press available, 11p.
Africa, Botswana
deposit - Orapa
Abstract: Spatially resolved analyses reveal considerable isotopic heterogeneity within and among diamonds ranging in size from 0.15 to 4.75 mm from the Orapa Mine, Botswana. The isotopic data are interpreted in conjunction with nitrogen aggregation state data and growth zone relationships from cathodoluminescence images. The integrated information confirms that a distinct diamond growth event (with low IaAB nitrogen aggregation states, moderately high nitrogen contents and ?13C and ?15N values compatible with average mantle values) is younger than the dominant population(s) of Type IaAB diamonds and cores of composite diamonds with more negative and positive ?13C and ?15N values, respectively. A significant proportion of the older diamond generation has high nitrogen contents, well outside the limit sector relationship, and these diamonds are likely to reflect derivation from subducted organic matter. Diamonds with low ?13C values combined with high nitrogen contents and positive ?15N values have not been previously widely recognised, even in studies of diamonds from Orapa. This may have been caused by prior analytical bias towards inclusion-bearing diamonds that are not necessarily representative of the entire range of diamond populations, and because of average measurements from heterogeneous diamonds measured by bulk combustion methods. Two distinct low nitrogen/Type II microdiamond populations were recognised that do not appear to continue into the macrodiamond sizes in the samples studied. Other populations, e.g. those containing residual singly-substituted nitrogen defects, range in size from small microdiamonds to large macrodiamonds. The total diamond content of the Orapa kimberlite thus reflects a complex assortment of multiple diamond populations.
Mineralogy and Petrology, in press available, 14p.
Africa, South Africa
deposit - Bultfontein
Abstract: MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) and PIC (Phlogopite-Ilmenite-Clinopyroxene) xenoliths are thought to be formed by intense Bprimary^ mantle metasomatism. These rocks also display secondary features, such as cross-cutting veins and geochemical zonation of matrix minerals, which probably reflect latermetasomatic events. To investigate the nature and origin(s) of these secondary features, 28 MARID and PIC xenoliths from southern African kimberlites and orangeites have been studied. MARID-hosted veins contain both carbonate and Ti-rich phases (e.g., titanite, phlogopite), suggesting that they formed by the infiltration of a carbonated silicate melt. Elevated TiO2 contents in MARID matrix mineral rims are spatially associated with carbonate-dominated veins, suggesting a genetic relationship between vein formation and geochemical zonation. Spongy rims around primaryMARID and PIC clinopyroxene are depleted in Na2O andAl2O3 relative to their cores, possibly reflecting mineral dissolution in the xenoliths during ascent and emplacement of the entraining kimberlite. The preservation of compositional differences between primary and secondary phases in MARID and PIC xenoliths indicates that metasomatism occurred shortly before, or broadly coeval with, kimberlite/orangeite magmatism; otherwise, at typical mantle temperatures, such features would have quickly re-equilibrated. Increased Na2O in some mineral rims (e.g., K-richterite) may therefore reflect equilibration with a more Na-enriched primitive kimberlite melt composition than is commonly suggested. Vein-hosted clinopyroxene 87Sr/86Sri (0.70539 ± 0.00079) in one MARID sample is intermediate between primary clinopyroxene in the sample (0.70814 ± 0.00002) and the host Bultfontein kimberlite (0.70432 ± 0.00005), suggesting that vein minerals are derived from interactions between primary MARID phases and kimberlite-related melts/fluids. Sulfur isotope compositions of barite (?34SVCDT = +4.69 ‰) and sulfides (?34SVCDT = ?0.69 ‰) in carbonate veins reflect equilibration at temperatures of 850-900 °C, consistent with sulfurrich melt/fluid infiltration in the lithospheric mantle. In contrast, vein carbonate C-O isotope systematics (?13CVPDB = ?9.18 ‰ ?18OVSMOW = +17.22‰) are not typical of kimberlites or other mantle carbonates (?13CVPDB = ?3 to ?8‰ ?18OVSMOW = 6 to 9 ), and may represent post-emplacement hydrothermal interactions of the cooling kimberlite with crustal fluids. These constraints suggest protracted metasomatism of MARID rocks shortly before and during entrainment by the host kimberlite.
Russian Geology and Geophysics, Vol. 59, pp. 486-498.
Russia
deposit - Zarnitsa
Abstract: Mosaic diamonds from the Zarnitsa kimberlite (Daldyn field, Yakutian diamondiferous province) are morphologicaly and structurally similar to dark gray mosaic diamonds of varieties V and VII found frequently in placers of the northeastern Siberian craton. However, although being similar in microstructure, the two groups of diamonds differ in formation mechanism: splitting of crystals in the case of placer diamonds (V and VII) and growth by geometric selection in the Zarnitsa kimberlite diamonds. Selective growth on originally polycrystalline substrates in the latter has produced radial micro structures with grains coarsening rimward from distinctly polycrystalline cores. Besides the formation mechanisms, diamonds of the two groups differ in origin of mineral inclusions, distribution of defects and nitrogen impurity, and carbon isotope composition. Unlike the placer diamonds of varieties V and VII, the analyzed crystals from the Zarnitsa kimberlite enclose peridotitic minerals (olivines and subcalcic Cr-bearing pyropes) and have total nitrogen contents common to natural kimberlitic diamonds (0 to 1761 ppm) and typical mantle carbon isotope compositions (-1.9 to -6.2%c 513C; -4.2%c on average). The distribution of defect centers in the Zarnitsa diamond samples fits the annealing model implying that nitrogen aggregation decreases from core to rim.
Abstract: Cr-pyrope xenocrysts and associated inclusions of crichtonite-group minerals from the Internatsionalnaya kimberlite pipe were studied to provide new insights into processes in the lithospheric mantle beneath the Mirny kimberlite field, Siberian craton. Pyropes are predominantly of lherzolitic paragenesis (Cr2O3 2-6?wt%) and have trace-element spectra typical for garnets from fertile mantle (gradual increase in chondrite-normalized values from LREE to MREE-HREE). Crichtonite-group minerals commonly occur as monomineralic elongated inclusions, mostly in association with rutile, Mg-ilmenite and Cr-spinel within individual grains of pyrope. Sample INT-266 hosts intergrowth of crichtonite-group mineral and Cl-apatite, while sample INT-324 contains polymineralic apatite- and dolomite-bearing assemblages. Crichtonite-group minerals are Al-rich (1.1-4.5?wt% Al2O3), moderately Zr-enriched (1.3-4.3?wt% ZrO2), and are Ca-, Sr-, and occasionally Ba-dominant in terms of A-site occupancy; they also contain significant amounts of Na and LREE. T-estimates and chemical composition of Cr-pyropes imply that samples represent relatively low-T peridotite assemblages with ambient T ranging from 720 to 820°?. Projected onto the 35?mW/m2 cratonic paleogeotherm for the Mirny kimberlite field (Griffin et al., 1999b. Tectonophysics 310, 1-35), temperature estimates yield a P range of ~34-42?kbar (~110-130?km), which corresponds to a mantle domain in the uppermost part of the diamond stability field. The presence of crichtonite-group minerals in Cr-pyropes has petrological and geochemical implications as evidence for metasomatic enrichment of some incompatible elements in the lithospheric mantle beneath the Mirny kimberlite field. The genesis of Cr-pyropes with inclusions of crichtonite-group minerals is attributed to the percolation of Ca-Sr-Na-LREE-Zr-bearing carbonate-silicate metasomatic agents through Mg- and Cr-rich depleted peridotite protoliths. The findings of several potentially new members of the crichtonite group as inclusions in garnet extend existing knowledge on the compositions and occurrences of exotic titanates stable in the lithospheric mantle.
Mineralogy and Petrology, in press available, 10p.
South America, Brazil, Juina
deposit - Sao Luiz
Abstract: The most remarkable feature of the inclusion suite in ultradeep alluvial and kimberlitic diamonds from Sao Luiz (Juina area in Brazil) is the enormous range in Mg# [100xMg/(Mg?+?Fe)] of the ferropericlases (fper). The Mg-richer ferropericlases are from the boundary to the lower mantle or from the lower mantle itself when they coexist with ringwoodite or Mg- perovskite (bridgmanite). This, however, is not an explanation for the more Fe-rich members and a lowermost mantle or a “D” layer origin has been proposed for them. Such a suggested ultra-deep origin separates the Fe-rich fper-bearing diamonds from the rest of the Sao Luiz ultradeep diamond inclusion suite, which also contains Ca-rich phases. These are now thought to have an origin in the uppermost lower mantle and in the transition zone and to belong either to a peridotitic or mafic (subducted oceanic crust) protolith lithology. We analysed a new set of more Fe-rich ferropericlase inclusions from 10 Sao Luiz ultradeep alluvial diamonds for their Li isotope composition by solution MC-ICP-MS (multi collector inductively coupled plasma mass spectrometry), their major and minor elements by EPMA (electron probe micro-analyser) and their Li-contents by SIMS (secondary ion mass spectrometry), with the aim to understand the origin of the ferropericlase protoliths. Our new data confirm the wide range of ferropericlase Mg# that were reported before and augment the known lack of correlation between major and minor elements. Four pooled ferropericlase inclusions from four diamonds provided sufficient material to determine for the first time their Li isotope composition, which ranges from ?7Li?+?9.6 ‰ to ?3.9 ‰. This wide Li isotopic range encompasses that of serpentinized ocean floor peridotites including rodingites and ophicarbonates, fresh and altered MORB (mid ocean ridge basalt), seafloor sediments and of eclogites. This large range in Li isotopic composition, up to 5 times higher than ‘primitive upper mantle’ Li-abundances, and an extremely large and incoherent range in Mg# and Cr, Ni, Mn, Na contents in the ferropericlase inclusions suggests that their protoliths were members of the above lithologies. This mélange of altered rocks originally contained a variety of carbonates (calcite, magnesite, dolomite, siderite) and brucite as the secondary products in veins and as patches and Ca-rich members like rodingites and ophicarbonates. Dehydration and redox reactions during or after deep subduction into the transition zone and the upper parts of the lower mantle led to the formation of diamond and ferropericlase inclusions with variable compositions and a predominance of the Ca-rich, high-pressure silicate inclusions. We suggest that the latter originated from peridotites, mafic rocks and sedimentary rocks as redox products between calcite and SiO2.
Mineralogy and Petrology, in press available, 12p.
Canada, Ontario, Attawapiskat
deposit - Victor
Abstract: The Jurassic Victor kimberlite (Attawapiskat Field) was emplaced into an area of the central Superior Craton that was affected by a lithosphere-scale thermal event at ~1.1 Ga. Victor diamonds formed ca. 400 million years after this event, in a lithospheric mantle characterized by an unusually cool model geotherm (37-38 mW/m2; Hasterok and Chapman 2011). The bulk of Victor diamonds derives from a thin (<10 km thick) layer that is located at about 180 km depth and represents lherzolitic substrates (for 85% of diamonds). Geothermobarometric calculations (average pressure and temperature at the 1 sigma level are 57?±?2 kbar and 1129?±?16 °C) coupled with typical fluid metasomatism-associated trace element patterns for garnet inclusions indicate diamond precipitation under sub-solidus (lherzolite + H2O) conditions. This conclusion links the presence of a diamond-rich lherzolitic layer in the lithospheric mantle, just above the depth where ascending melts would freeze, to the unusually low paleogeotherm beneath Attawapiskat, because along an average cratonic geotherm (40 mW/m2) lherzolite in the presence of hydrous fluid would melt at depths >140 km.
Lithos, DOI:10.1016 /j.lithos.2018 .05.027 available 52p.
Russia
deposit - Udachnaya
Abstract: A suite of seventeen unique, large, and fresh eclogite xenoliths from the Udachnaya pipe have been studied for their whole-rock and mineral major- and trace-element compositions. Based on their major-element compositions, the Udachnaya eclogites can be subdivided in two groups: high magnesian (Mg# 68.8-81.9) and low magnesian (Mg# 56.8-59). The two eclogite groups are clearly different in the style of correlation between major elements. Positive correlations of FeO and CaO with MgO are observed in the low-magnesian group, whereas these correlations are negative in the high-magnesian group. In terms of trace element composition, the Udachnaya eclogites are enriched over Primitive Mantle, but comparable to mid-ocean-ridge basalt composition, except for significant enrichment in large-ion lithophile elements (LILE; Rb, Ba, K, Sr). Most of the samples show a positive Eu anomaly, irrespective of group. Reconstructed whole-rock composition from clinopyroxene and garnet modal abundances contains much less incompatible elements (LILE, light rare earth elements, high field strength elements) than measured composition. Approximately 60 to 100% of the middle rare earth elements, Zr, and Hf, and nearly 100% of the heavy rare earth elements, Co, V, and Sc of the whole-rock budget are concentrated in Gar and Cpx. Variations in major element compositions cover a full section of the modern and Archaean oceanic crust, from troctolite, through gabbroic rocks, to basalts. The low-Mg# eclogites could have formed from upper oceanic crust protoliths, being a mixture of basalts and gabbro, whereas the high-Mg# eclogites are originated from gabbro-troctolite section of the lower oceanic crust. Concordant variations of Eu anomaly with the Lu/Sr ratio and the V and Ni contents in the eclogite compositions are in agreement with the fractionation of plagioclase, clinopyroxene, and olivine in their low-pressure precursor rocks. Negative correlations of SiO2 and MgO, and a low Nd/YbNMORB ratio, in the low-Mg# eclogites are in agreement with partial melt loss, but the presence of accessory quartz limits the degree of melting to 13%. Major and trace element compositions suggest that the high-Mg# eclogites, and, consequently, the lower oceanic crust, could not have experienced significant melt loss, and subduction in the Archaean may have been essentially dry, compared to the present day.
Mineralogy and Petrology, 10.1007/s00710 -018-0599-2, 14p.
Canada, Northwest Territories
deposit - Diavik, Ekati
Abstract: Kimberlites from the Diavik and Ekati diamond mines in the Lac de Gras kimberlite field contain abundant large (>1 cm) clinopyroxene (Cr-diopside) and garnet (Cr-pyrope) crystals. We present the first extensive mineral chemical dataset for these megacrysts from Diavik and Ekati and compare their compositions to cratonic peridotites and megacrysts from the Slave and other cratons. The Diavik and Ekati Cr-diopside and Cr-pyrope megacrysts are interpreted to belong to the Cr-rich megacryst suite. Evidence for textural, compositional, and isotopic disequilibrium suggests that they constitute xenocrysts in their host kimberlites. Nevertheless, their formation may be linked to extensive kimberlite magmatism and accompanying mantle metasomatism preceding the eruption of their host kimberlites. It is proposed that the formation of megacrysts may be linked to failed kimberlites. In this scheme, the Cr-rich megacrysts are formed by progressive interaction of percolating melts with the surrounding depleted mantle (originally harzburgite). As these melts percolate outwards, they may contribute to the introduction of clinopyroxene and garnet into the depleted mantle, thereby forming lherzolite. This model hinges on the observation that lherzolitic clinopyroxenes and garnets at Lac de Gras have compositions that are strikingly similar to those of the Cr-rich megacrysts, in terms of major and trace elements, as well as Sr isotopes. As such, the Cr-rich megacrysts may have implications for the origin of clinopyroxene and garnet in cratonic lherzolites worldwide.
Mineralogy and Petrology, 10.1007/s00710 -018-0599-2, 14p.
Canada, Northwest Territories
deposit - Diavik, Ekati
Abstract: Kimberlites from the Diavik and Ekati diamond mines in the Lac de Gras kimberlite field contain abundant large (>1 cm) clinopyroxene (Cr-diopside) and garnet (Cr-pyrope) crystals. We present the first extensive mineral chemical dataset for these megacrysts from Diavik and Ekati and compare their compositions to cratonic peridotites and megacrysts from the Slave and other cratons. The Diavik and Ekati Cr-diopside and Cr-pyrope megacrysts are interpreted to belong to the Cr-rich megacryst suite. Evidence for textural, compositional, and isotopic disequilibrium suggests that they constitute xenocrysts in their host kimberlites. Nevertheless, their formation may be linked to extensive kimberlite magmatism and accompanying mantle metasomatism preceding the eruption of their host kimberlites. It is proposed that the formation of megacrysts may be linked to failed kimberlites. In this scheme, the Cr-rich megacrysts are formed by progressive interaction of percolating melts with the surrounding depleted mantle (originally harzburgite). As these melts percolate outwards, they may contribute to the introduction of clinopyroxene and garnet into the depleted mantle, thereby forming lherzolite. This model hinges on the observation that lherzolitic clinopyroxenes and garnets at Lac de Gras have compositions that are strikingly similar to those of the Cr-rich megacrysts, in terms of major and trace elements, as well as Sr isotopes. As such, the Cr-rich megacrysts may have implications for the origin of clinopyroxene and garnet in cratonic lherzolites worldwide.
Mineralogy and Petrology, June 14, DOI:10.1007/ s00710-018- 0593-8, 14p.
Africa, Botswana
deposit - Nxau
Abstract: The Nxau Nxau kimberlites in northwest Botswana belong to the Xaudum kimberlite province that also includes the Sikereti, Kaudom and Gura kimberlite clusters in north-east Namibia. The Nxau Nxau kimberlites lie on the southernmost extension of the Congo Craton, which incorporates part of the Damara Orogenic Belt on its margin. The Xaudum kimberlite province is geographically isolated from other known clusters but occurs within the limits of the NW-SE oriented, Karoo-aged Okavango Dyke Swarm and near NE-SW faults interpreted as the early stages of the East African Rift System. Petrographic, geochronological and isotopic studies were undertaken to characterise the nature of these kimberlites and the timing of their emplacement. The Nxau Nxau kimberlites exhibit groundmass textures, mineral phases and Sr-isotope compositions (87Sr/86Sri of 0.7036?±?0.0002; 2?) that are characteristic of archetypal (Group I) kimberlites. U-Pb perovskite, 40Ar/39Ar phlogopite and Rb-Sr phlogopite ages indicate that the kimberlites were emplaced in the Cretaceous, with perovskite from four samples yielding a preferred weighted average U-Pb age of 84?±?4 Ma (2?). This age is typical of many kimberlites in southern Africa, indicating that the Xaudum occurrences form part of this widespread Late Cretaceous kimberlite magmatic province. This time marks a significant period of tectonic stress reorganisation that could have provided the trigger for kimberlite magmatism. In this regard, the Nxau Nxau kimberlites may form part of a NE-SW oriented trend such as the Lucapa corridor, with implications for further undiscovered kimberlites along this corridor.
Abstract: The diamondiferous Jwaneng kimberlite cluster (~240 Ma) is located on the NW rim of the Archaean Kaapvaal Craton in central Botswana. Previous studies report eclogitic diamond formation in the late Archean (2.9 Ga) and in the Middle Proterozoic (1.5 Ga) involving different mantle and sedimentary components [1;2;3]. Here we report newly acquired Sm- Nd ages of individual eclogitic pyrope-almandine and omphacite inclusions along with their major element data and nitrogen data from the diamond hosts to re-examine Jwaneng’s diamond formation ages. The Sm-Nd isotope analyses were performed via TIMS using 1013? resistors [4]. An initial suite of three pyropealmandine and 14 omphacite inclusions yield 143Nd/144Nd from 0.51102±7 to 0.5155±5. 147Sm/144Nd vary from 0.024 to 0.469. Major element data defines two inclusion populations: (1) seven omphacites with high Mg#, high Cr# and one pyropealmandine with low-Ca define an isochron age of 1.93±0.16 Ga with ?Ndi= +3.5; (2) seven omphacites with low Mg#, low Cr# and two pyrope-almandines with low-Ca define an isochron age of 0.82±0.06 Ga with ?Ndi= +3.7. Nitrogen contents of corresponding diamond host growth zones in Group (1) are ? 50 at.ppm whereas Group (2) range between 50 to 700 at.ppm with N-aggregation > 70 %B. Additional data used to define “co-genetic” inclusion suites include Sr-isotopes and trace elements of the inclusions and carbon isotopes of the diamond hosts. Re-Os data of coexisting sulphide inclusions from the same silicate-bearing diamonds further validates the ages and indicates more periods of diamond formation at Jwaneng than previously assumed. The integrated data indicate the possibility of an extensive Paleoproterozoic diamond-forming event in southern Africa.
Mineralogy and Petrology, June 14, DOI:10.1007/ s0710-018 -0578-7, 12p.
Canada, Nunavut
deposit - Chidliak
Abstract: Exploration for diamond-bearing kimberlites in the Chidliak project area by Peregrine Diamonds has generated a grid-like till sampling pattern across four discrete areas of interest totalling 402 km2 that is densely populated with research-grade compositional data for 10,743 mantle-derived Cr-pyrope garnets. The available dataset is well suited to statistical analysis, in part due to the relatively unbiased spatial coverage. Previous workers showed empirically that the TiO2 and Mn thermometry (Ti-TMn) attributes of Cr-pyrope populations at the Chidliak project may serve as source-specific “fingerprints”. In this work, we employ a simplified version of the multivariate Mahalanobis distance technique to formally examine the variability of, and differences between, Ti-TMn attributes of Cr-pyrope subpopulations recovered from a Laurentide-age glaciated terrain that also contains 30 known kimberlites within the four areas of interest. We show the simplified Mahalanobis distance approach enables accurate discrimination of Cr-pyrope subpopulations with subtly to distinctly different Ti-TMn attributes, and permits proper demarcation of their respective kimberlite source(s), specifically in areas with straightforward glacial histories. Redistribution and blending of Cr-pyrope subpopulations from known kimberlite sources is also observed, and typifies areas at Chidliak with complex late-glacial histories. Our results support <1 km horizontal scale subtle to obvious variability in the proportions of TiO2-rich and high-temperature (> 1100 °C) Cr-pyropes between closely spaced kimberlite source(s) and also between physically adjacent magma batches within single kimberlite pipes. The local scale variability is attributed to protokimberlite fluid or melt interacting with, and metasomatizing discrete conduits within, the ambient diamond-facies peridotitic mantle at times closely preceding eruption of kimberlite magma batches at Chidliak.
Mineralogy and Petrology, 10.1007/ s00710-018- 0589-4, 14p.
Africa, South Africa, Canada, Northwest Territories, Ontario
deposit - Venetia, Voorspoed, Gahcho Kue, Victor, Snap Lake
Abstract: De Beers kimberlite mine operations in South Africa (Venetia and Voorspoed) and Canada (Gahcho Kué, Victor, and Snap Lake) have the potential to sequester carbon dioxide (CO2) through weathering of kimberlite mine tailings, which can store carbon in secondary carbonate minerals (mineral carbonation). Carbonation of ca. 4.7 to 24.0 wt% (average?=?13.8 wt%) of annual processed kimberlite production could offset 100% of each mine site’s carbon dioxide equivalent (CO2e) emissions. Minerals of particular interest for reactivity with atmospheric or waste CO2 from energy production include serpentine minerals, olivine (forsterite), brucite, and smectite. The most abundant minerals, such as serpentine polymorphs, provide the bulk of the carbonation potential. However, the detection of minor amounts of highly reactive brucite in tailings from Victor, as well as the likely presence of brucite at Venetia, Gahcho Kué, and Snap Lake, is also important for the mineral carbonation potential of the mine sites.
Mineralogy and Petrology, 10.1007/ s00710-018- 0589-4, 14p.
Africa, South Africa, Canada, Northwest Territories, Ontario
deposit - Venetia, Voorspoed, Gahcho Kue, Victor, Snap Lake
Abstract: De Beers kimberlite mine operations in South Africa (Venetia and Voorspoed) and Canada (Gahcho Kué, Victor, and Snap Lake) have the potential to sequester carbon dioxide (CO2) through weathering of kimberlite mine tailings, which can store carbon in secondary carbonate minerals (mineral carbonation). Carbonation of ca. 4.7 to 24.0 wt% (average?=?13.8 wt%) of annual processed kimberlite production could offset 100% of each mine site’s carbon dioxide equivalent (CO2e) emissions. Minerals of particular interest for reactivity with atmospheric or waste CO2 from energy production include serpentine minerals, olivine (forsterite), brucite, and smectite. The most abundant minerals, such as serpentine polymorphs, provide the bulk of the carbonation potential. However, the detection of minor amounts of highly reactive brucite in tailings from Victor, as well as the likely presence of brucite at Venetia, Gahcho Kué, and Snap Lake, is also important for the mineral carbonation potential of the mine sites.
Mineralogy and Petrology, 10.1007/ s00710-018- 0589-4, 14p.
Africa, South Africa, Canada, Northwest Territories, Ontario
deposit - Venetia, Voorspoed, Gahcho Kue, Victor, Snap Lake
Abstract: De Beers kimberlite mine operations in South Africa (Venetia and Voorspoed) and Canada (Gahcho Kué, Victor, and Snap Lake) have the potential to sequester carbon dioxide (CO2) through weathering of kimberlite mine tailings, which can store carbon in secondary carbonate minerals (mineral carbonation). Carbonation of ca. 4.7 to 24.0 wt% (average?=?13.8 wt%) of annual processed kimberlite production could offset 100% of each mine site’s carbon dioxide equivalent (CO2e) emissions. Minerals of particular interest for reactivity with atmospheric or waste CO2 from energy production include serpentine minerals, olivine (forsterite), brucite, and smectite. The most abundant minerals, such as serpentine polymorphs, provide the bulk of the carbonation potential. However, the detection of minor amounts of highly reactive brucite in tailings from Victor, as well as the likely presence of brucite at Venetia, Gahcho Kué, and Snap Lake, is also important for the mineral carbonation potential of the mine sites.
Mineralogy and Petrology, 10.1007/ s00710-018- 0589-4, 14p.
Africa, South Africa, Canada, Northwest Territories, Ontario
deposit - Venetia, Voorspoed, Gahcho Kue, Victor, Snap Lake
Abstract: De Beers kimberlite mine operations in South Africa (Venetia and Voorspoed) and Canada (Gahcho Kué, Victor, and Snap Lake) have the potential to sequester carbon dioxide (CO2) through weathering of kimberlite mine tailings, which can store carbon in secondary carbonate minerals (mineral carbonation). Carbonation of ca. 4.7 to 24.0 wt% (average?=?13.8 wt%) of annual processed kimberlite production could offset 100% of each mine site’s carbon dioxide equivalent (CO2e) emissions. Minerals of particular interest for reactivity with atmospheric or waste CO2 from energy production include serpentine minerals, olivine (forsterite), brucite, and smectite. The most abundant minerals, such as serpentine polymorphs, provide the bulk of the carbonation potential. However, the detection of minor amounts of highly reactive brucite in tailings from Victor, as well as the likely presence of brucite at Venetia, Gahcho Kué, and Snap Lake, is also important for the mineral carbonation potential of the mine sites.
Mineralogy and Petrology, 10.1007/ s00710-018- 0589-4, 14p.
Africa, South Africa, Canada, Northwest Territories, Ontario
deposit - Venetia, Voorspoed, Gahcho Kue, Victor, Snap Lake
Abstract: De Beers kimberlite mine operations in South Africa (Venetia and Voorspoed) and Canada (Gahcho Kué, Victor, and Snap Lake) have the potential to sequester carbon dioxide (CO2) through weathering of kimberlite mine tailings, which can store carbon in secondary carbonate minerals (mineral carbonation). Carbonation of ca. 4.7 to 24.0 wt% (average?=?13.8 wt%) of annual processed kimberlite production could offset 100% of each mine site’s carbon dioxide equivalent (CO2e) emissions. Minerals of particular interest for reactivity with atmospheric or waste CO2 from energy production include serpentine minerals, olivine (forsterite), brucite, and smectite. The most abundant minerals, such as serpentine polymorphs, provide the bulk of the carbonation potential. However, the detection of minor amounts of highly reactive brucite in tailings from Victor, as well as the likely presence of brucite at Venetia, Gahcho Kué, and Snap Lake, is also important for the mineral carbonation potential of the mine sites.
Mineralogy and Petrology, 10.1007/ s710-018-0576 -9, 10p.
South America, Brazil
deposit - Sao Luiz
Abstract: Three diamonds from Sao Luiz, Brazil carrying nano- and micro-inclusions of molecular ?-N2 that exsolved at the base of the transition zone were studied for their C and N isotopic composition and the concentration of N utilizing SIMS. The diamonds are individually uniform in their C isotopic composition and most spot analyses yield ?13C values of ?3.2?±?0.1‰ (ON-SLZ-390) and???4.7?±?0.1‰ (ON-SLZ-391 and 392). Only a few analyses deviate from these tight ranges and all fall within the main mantle range of ?5?±?3‰. Most of the N isotope analyses also have typical mantle ?15N values (?6.6?±?0.4‰, ?3.6?±?0.5‰ and???4.1?±?0.6‰ for ON-SLZ-390, 391 and 392, respectively) and are associated with high N concentrations of 800-1250 atomic ppm. However, some N isotopic ratios, associated with low N concentrations (<400 ppm) and narrow zones with bright luminescence are distinctly above the average, reaching positive ?15N values. These sharp fluctuations cannot be attributed to fractionation. They may reflect arrival of new small pulses of melt or fluid that evolved under different conditions. Alternatively, they may result from fractionation between different growth directions, so that distinct ?15N values and N concentrations may form during diamond growth from a single melt/fluid. Other more continuous variations, in the core of ON-SLZ-390 or the rim of ON-SLZ-392 may be the result of Rayleigh fractionation or mixing.
Mineralogy and Petrology, June 14, DOI:10.1007/ s00710-018 -0595-6, 16p.
Africa, South Africa
deposit - Boshof
Abstract: We describe the petrography and mineral chemistry of sixteen eclogite and garnet pyroxenite xenoliths from the reworked Boshof road dump (Kimberley) and define three groups that stem from different depths. Group A, the shallowest derived, has low HREE (heavy rare earth element) abundances, flat middle to heavy REE patterns and high Mg# [= 100•Mg/(Mg?+?Fe)]. Their protoliths probably were higher pressure cumulates (~ 0.7 GPa) of mainly clinopyroxene (cpx) and subordinate orthopyroxene (opx) and olivine (ol). Group B1 xenoliths, derived from the graphite/diamond boundary and below show similarities to present-day N-MORB that were modified by partial melting (higher Mg# and positively inclined MREE (middle REE) and HREE (heavy REE) patterns of calculated bulk rocks). Group B2 samples from greatest depth are unique amongst eclogites reported so far worldwide. The calculated bulk rocks have humped REE patterns with very low La and Lu and prominent maxima at Sm or Eu and anomalously high Na2O (up to 5 wt%) which makes protolith identification difficult. The complex trace element signatures of the full spectrum of Kimberley eclogites belie a multi-stage history of melt depletion and metasomatism with the introduction of new phases especially of phlogopite (phlog). Phlogopite appears to be characteristic for Kimberley eclogites and garnet peridotites. Modelling the metasomatic overprint indicates that groups A and B1 were overprinted by volatile- and potassium-rich melts probably by a process of chromatographic fractionation. Using constraints from other metasomatized Kimberley mantle rocks suggest that much of the metasomatic phlogopite in the eclogites formed during an intense episode of metasomatism that affected the mantle beneath this region 1.1 Gyr ago.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018- 0587-6 16p.
Africa, Sierra Leone
deposit - Zimmi
Abstract: Zimmi diamonds (Sierra Leone) have 500 million year mantle residency times whose origin is best explained by rapid tectonic exhumation to shallower depths in the mantle, associated with continental collision but prior to kimberlite eruption. Here we present spectroscopic data for a new suite of Zimmi sulphide-bearing diamonds that allow us to evaluate the link between their spectroscopic features and their unusual geological history. Cathodoluminesence (CL) imaging of these diamonds revealed irregular patterns with abundant deformation lamellae, associated with the diamonds' tectonic exhumation. Vacancies formed during deformation were subsequently naturally annealed to form vacancy clusters, NV0/- centres and H3 (NVN0). The brownish-yellow to greenish-yellow colours observed in Zimmi Ib-IaA diamonds result from visible absorption by a combination of isolated substitutional nitrogen ( {N}S^0 ) and deformation-related vacancy clusters. Colour-forming centres and other spectroscopic features can all be attributed to the unique geological history of Zimmi Ib-IaA diamonds and their rapid exhumation after formation.
Mineralogy and Petrology, June 14, DOI:10.1007/ s00710-018 -0588-5, 16p.
Africa, South Africa
deposit - De Beers dyke
Abstract: We present petrographic and mineral chemical data for a suite of samples derived from the De Beers dyke, a contemporaneous, composite intrusion bordering the De Beers pipe (Kimberley, South Africa). Petrographic features and mineral compositions indicate the following stages in the evolution of this dyke: (1) production of antecrystic material by kimberlite-related metasomatism in the mantle (i.e., high Cr-Ti phlogopite); (2) entrainment of wall-rock material during ascent through the lithospheric mantle, including antecrysts; (3) early magmatic crystallisation of olivine (internal zones and subsequently rims), Cr-rich spinel, rutile, and magnesian ilmenite, probably on ascent to the surface; and (4) crystallisation of groundmass phases (i.e., olivine rinds, Fe-Ti-rich spinels, perovskite, apatite, monticellite, calcite micro-phenocrysts, kinoshitalite-phlogopite, barite, and baddeleyite) and the mesostasis (calcite, dolomite, and serpentine) on emplacement in the upper crust. Groundmass and mesostasis crystallisation likely forms a continuous sequence with deuteric/hydrothermal modification. The petrographic features, mineralogy, and mineral compositions of different units within the De Beers dyke are indistinguishable from one another, indicating a common petrogenesis. The compositions of antecrysts (i.e., high Cr-Ti phlogopite) and magmatic phases (e.g., olivine rims, magnesian ilmenite, and spinel) overlap those from the root zone intrusions of the main Kimberley pipes (i.e., Wesselton, De Beers, Bultfontein). However, the composition of these magmatic phases is distinct from those in ‘evolved’ intrusions of the Kimberley cluster (e.g., Benfontein, Wesselton water tunnel sills). Although the effects of syn-emplacement flow processes are evident (e.g., alignment of phases parallel to contacts), there is no evidence that the De Beers dyke has undergone significant pre-emplacement crystal fractionation (e.g., olivine, spinel, ilmenite). This study demonstrates the requirement for detailed petrographic and mineral chemical studies to assess whether individual intrusions are in fact ‘evolved’; and that dykes are not necessarily produced by differentiated magmas.
Mineralogy and Petrology, 10.1007/ s710-018-0592 -9, 10p.
Africa, Botswana
deposit - Orapa, Damtshaa, BK09, BK12,AK01
Abstract: Twenty eclogitic diamonds from Orapa Mine (Botswana) with an unusual yellow colour are characterised for their growth structure, N systematics, and C isotope composition, and the major element composition of their silicate inclusions. The diamonds show complex luminescence with green, blue and non-luminescent zones and occasional sector zonation. All parts of the diamonds have low total N concentrations (<50 at.ppm, with one exception of <125 at.ppm) and a limited range in C isotope composition (?5.7 to ?10.6‰). Fourier Transform Infrared spectra show bands at 1334, 1332, 1282, and 1240 cm?1 typical for Ib-IaA diamonds. Relict unaggregated N defects (Nso and Ns+) are present and the preservation is likely caused by the low N concentrations and possible low mantle residence temperatures rather than young diamond formation (inclusion ages of 140, 1096, 1699 Ma; Timmerman et al. Earth Planet Sc Lett 463:178-188, 2017). Garnet and clinopyroxene inclusions extracted from 14 diamonds have an eclogitic composition with relatively low Ca contents and based on all characteristics, these diamonds form a distinct population from Orapa.
Mineralogy and Petrology, 10.1007/ s710-018-0592 -9, 10p.
Africa, Botswana
deposit - Orapa, Damtshaa, BK09, BK12,AK01
Abstract: Twenty eclogitic diamonds from Orapa Mine (Botswana) with an unusual yellow colour are characterised for their growth structure, N systematics, and C isotope composition, and the major element composition of their silicate inclusions. The diamonds show complex luminescence with green, blue and non-luminescent zones and occasional sector zonation. All parts of the diamonds have low total N concentrations (<50 at.ppm, with one exception of <125 at.ppm) and a limited range in C isotope composition (?5.7 to ?10.6‰). Fourier Transform Infrared spectra show bands at 1334, 1332, 1282, and 1240 cm?1 typical for Ib-IaA diamonds. Relict unaggregated N defects (Nso and Ns+) are present and the preservation is likely caused by the low N concentrations and possible low mantle residence temperatures rather than young diamond formation (inclusion ages of 140, 1096, 1699 Ma; Timmerman et al. Earth Planet Sc Lett 463:178-188, 2017). Garnet and clinopyroxene inclusions extracted from 14 diamonds have an eclogitic composition with relatively low Ca contents and based on all characteristics, these diamonds form a distinct population from Orapa.
Mineralogy and Petrology, 10.1007/ s710-018-0592 -9, 10p.
Africa, Botswana
deposit - Orapa, Damtshaa, BK09, BK12,AK01
Abstract: Twenty eclogitic diamonds from Orapa Mine (Botswana) with an unusual yellow colour are characterised for their growth structure, N systematics, and C isotope composition, and the major element composition of their silicate inclusions. The diamonds show complex luminescence with green, blue and non-luminescent zones and occasional sector zonation. All parts of the diamonds have low total N concentrations (<50 at.ppm, with one exception of <125 at.ppm) and a limited range in C isotope composition (?5.7 to ?10.6‰). Fourier Transform Infrared spectra show bands at 1334, 1332, 1282, and 1240 cm?1 typical for Ib-IaA diamonds. Relict unaggregated N defects (Nso and Ns+) are present and the preservation is likely caused by the low N concentrations and possible low mantle residence temperatures rather than young diamond formation (inclusion ages of 140, 1096, 1699 Ma; Timmerman et al. Earth Planet Sc Lett 463:178-188, 2017). Garnet and clinopyroxene inclusions extracted from 14 diamonds have an eclogitic composition with relatively low Ca contents and based on all characteristics, these diamonds form a distinct population from Orapa.
Mineralogy and Petrology, 10.1007/ s710-018-0592 -9, 10p.
Africa, Botswana
deposit - Orapa, Damtshaa, BK09, BK12,AK01
Abstract: Twenty eclogitic diamonds from Orapa Mine (Botswana) with an unusual yellow colour are characterised for their growth structure, N systematics, and C isotope composition, and the major element composition of their silicate inclusions. The diamonds show complex luminescence with green, blue and non-luminescent zones and occasional sector zonation. All parts of the diamonds have low total N concentrations (<50 at.ppm, with one exception of <125 at.ppm) and a limited range in C isotope composition (?5.7 to ?10.6‰). Fourier Transform Infrared spectra show bands at 1334, 1332, 1282, and 1240 cm?1 typical for Ib-IaA diamonds. Relict unaggregated N defects (Nso and Ns+) are present and the preservation is likely caused by the low N concentrations and possible low mantle residence temperatures rather than young diamond formation (inclusion ages of 140, 1096, 1699 Ma; Timmerman et al. Earth Planet Sc Lett 463:178-188, 2017). Garnet and clinopyroxene inclusions extracted from 14 diamonds have an eclogitic composition with relatively low Ca contents and based on all characteristics, these diamonds form a distinct population from Orapa.
Mineralogy and Petrology, 10.1007/ s710-018-0592 -9, 10p.
Africa, Botswana
deposit - Orapa, Damtshaa, BK09, BK12,AK01
Abstract: Twenty eclogitic diamonds from Orapa Mine (Botswana) with an unusual yellow colour are characterised for their growth structure, N systematics, and C isotope composition, and the major element composition of their silicate inclusions. The diamonds show complex luminescence with green, blue and non-luminescent zones and occasional sector zonation. All parts of the diamonds have low total N concentrations (<50 at.ppm, with one exception of <125 at.ppm) and a limited range in C isotope composition (?5.7 to ?10.6‰). Fourier Transform Infrared spectra show bands at 1334, 1332, 1282, and 1240 cm?1 typical for Ib-IaA diamonds. Relict unaggregated N defects (Nso and Ns+) are present and the preservation is likely caused by the low N concentrations and possible low mantle residence temperatures rather than young diamond formation (inclusion ages of 140, 1096, 1699 Ma; Timmerman et al. Earth Planet Sc Lett 463:178-188, 2017). Garnet and clinopyroxene inclusions extracted from 14 diamonds have an eclogitic composition with relatively low Ca contents and based on all characteristics, these diamonds form a distinct population from Orapa.
Mineralogy and Petrology, 10.1007/ s710-018- 0603-x 15p.
Africa, South Africa
deposit - Finsch, De Beers Pool, Koffiefontein
Abstract: Fibrous diamond growth zones often contain abundant high-density fluid (HDF) inclusions and these provide the most direct information on diamond-forming fluids. Noble gases are incompatible elements and particularly useful in evaluating large-scale mantle processes. This study further constrains the evolution and origin of the HDFs by combining noble gas systematics with ?¹³C, N concentrations, and fluid inclusion compositions for 21 individual growth zones in 13 diamonds from the Finsch (n = 3), DeBeers Pool (n = 7), and Koffiefontein (n = 3) mines on the Kaapvaal Craton. C isotope compositions range from ?2.8 to ?8.6‰ and N contents vary between 268 and 867 at.ppm, except for one diamond with contents of <30 at.ppm N. Nine of the thirteen studied diamonds contained saline HDF inclusions, but the other four diamonds had carbonatitic or silicic HDF inclusions. Carbonatitic and silicic HDFs yielded low He concentrations, R/Ra (³He/?Hesample/³He/?Heair) values of 3.2–6.7, and low ??Ar/³?Ar ratios of 390–1940. Noble gas characteristics of carbonatitic-silicic HDFs appear consistent with a subducted sediment origin and interaction with eclogite. Saline HDFs are characterised by high He concentrations, with R/Ra mostly between 3.9 and 5.7, and a wide range in ??Ar/³?Ar ratios (389–30,200). The saline HDFs likely originated from subducted oceanic crust with low He but moderate Ar contents. Subsequent interaction of these saline HDFs with mantle peridotite could explain the increase in He concentrations and mantle-like He isotope composition, with the range in low to high ??Ar/³?Ar ratios dependent on the initial ³?Ar content and extent of lithosphere interaction. The observed negative correlation between ?He contents and R/Ra values in saline HDFs indicates significant in situ radiogenic ?He production.
Noble gas geochemistry of fluid inclusions in South African diamonds: implications for the origin of diamond-forming fluids.
Mineralogy and Petrology, 10.1007/ s710-018- 0603-x 15p.
Africa, South Africa
deposit - Finsch, De Beers Pool, Koffiefontein
Abstract: Fibrous diamond growth zones often contain abundant high-density fluid (HDF) inclusions and these provide the most direct information on diamond-forming fluids. Noble gases are incompatible elements and particularly useful in evaluating large-scale mantle processes. This study further constrains the evolution and origin of the HDFs by combining noble gas systematics with ?¹³C, N concentrations, and fluid inclusion compositions for 21 individual growth zones in 13 diamonds from the Finsch (n = 3), DeBeers Pool (n = 7), and Koffiefontein (n = 3) mines on the Kaapvaal Craton. C isotope compositions range from ?2.8 to ?8.6‰ and N contents vary between 268 and 867 at.ppm, except for one diamond with contents of <30 at.ppm N. Nine of the thirteen studied diamonds contained saline HDF inclusions, but the other four diamonds had carbonatitic or silicic HDF inclusions. Carbonatitic and silicic HDFs yielded low He concentrations, R/Ra (³He/?Hesample/³He/?Heair) values of 3.2–6.7, and low ??Ar/³?Ar ratios of 390–1940. Noble gas characteristics of carbonatitic-silicic HDFs appear consistent with a subducted sediment origin and interaction with eclogite. Saline HDFs are characterised by high He concentrations, with R/Ra mostly between 3.9 and 5.7, and a wide range in ??Ar/³?Ar ratios (389–30,200). The saline HDFs likely originated from subducted oceanic crust with low He but moderate Ar contents. Subsequent interaction of these saline HDFs with mantle peridotite could explain the increase in He concentrations and mantle-like He isotope composition, with the range in low to high ??Ar/³?Ar ratios dependent on the initial ³?Ar content and extent of lithosphere interaction. The observed negative correlation between ?He contents and R/Ra values in saline HDFs indicates significant in situ radiogenic ?He production.
Noble gas geochemistry of fluid inclusions in South African diamonds: implications for the origin of diamond-forming fluids.
Mineralogy and Petrology, 10.1007/ s710-018- 0603-x 15p.
Africa, South Africa
deposit - Finsch, De Beers Pool, Koffiefontein
Abstract: Fibrous diamond growth zones often contain abundant high-density fluid (HDF) inclusions and these provide the most direct information on diamond-forming fluids. Noble gases are incompatible elements and particularly useful in evaluating large-scale mantle processes. This study further constrains the evolution and origin of the HDFs by combining noble gas systematics with ?¹³C, N concentrations, and fluid inclusion compositions for 21 individual growth zones in 13 diamonds from the Finsch (n = 3), DeBeers Pool (n = 7), and Koffiefontein (n = 3) mines on the Kaapvaal Craton. C isotope compositions range from ?2.8 to ?8.6‰ and N contents vary between 268 and 867 at.ppm, except for one diamond with contents of <30 at.ppm N. Nine of the thirteen studied diamonds contained saline HDF inclusions, but the other four diamonds had carbonatitic or silicic HDF inclusions. Carbonatitic and silicic HDFs yielded low He concentrations, R/Ra (³He/?Hesample/³He/?Heair) values of 3.2–6.7, and low ??Ar/³?Ar ratios of 390–1940. Noble gas characteristics of carbonatitic-silicic HDFs appear consistent with a subducted sediment origin and interaction with eclogite. Saline HDFs are characterised by high He concentrations, with R/Ra mostly between 3.9 and 5.7, and a wide range in ??Ar/³?Ar ratios (389–30,200). The saline HDFs likely originated from subducted oceanic crust with low He but moderate Ar contents. Subsequent interaction of these saline HDFs with mantle peridotite could explain the increase in He concentrations and mantle-like He isotope composition, with the range in low to high ??Ar/³?Ar ratios dependent on the initial ³?Ar content and extent of lithosphere interaction. The observed negative correlation between ?He contents and R/Ra values in saline HDFs indicates significant in situ radiogenic ?He production.
Noble gas geochemistry of fluid inclusions in South African diamonds: implications for the origin of diamond-forming fluids.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-06174 12p.
Russia, Siberia
deposit - Mirny
Abstract: Here we present new data from a systematic Sr, Nd, O, C isotope and geochemical study of kimberlites of Devonian age Mirny field that are located in the southernmost part of the Siberian diamondiferous province. Major and trace element compositions of the Mirny field kimberlites show a significant compositional variability both between pipes and within one diatreme. They are enriched in incompatible trace elements with La/Yb ratios in the range of (65-00). Initial Nd isotope ratios calculated back to the time of the Mirny field kimberlite emplacement (t?=?360 ma) are depleted relative to the chondritic uniform reservoir (CHUR) model being 4 up to 6 ?Nd(t) units, suggesting an asthenospheric source for incompatible elements in kimberlites. Initial Sr isotope ratios are significantly variable, being in the range 0.70387-0.70845, indicating a complex source history and a strong influence of post-magmatic alteration. Four samples have almost identical initial Nd and Sr isotope compositions that are similar to the prevalent mantle (PREMA) reservoir. We propose that the source of the proto-kimberlite melt of the Mirny field kimberlites is the same as that for the majority of ocean island basalts (OIB). The source of the Mirny field kimberlites must possess three main features: It should be enriched with incompatible elements, be depleted in the major elements (Si, Al, Fe and Ti) and heavy rare earth elements (REE) and it should retain the asthenospheric Nd isotope composition. A two-stage model of kimberlite melt formation can fulfil those requirements. The intrusion of small bodies of this proto-kimberlite melt into lithospheric mantle forms a veined heterogeneously enriched source through fractional crystallization and metasomatism of adjacent peridotites. Re-melting of this source shortly after it was metasomatically enriched produced the kimberlite melt. The chemistry, mineralogy and diamond grade of each particular kimberlite are strongly dependent on the character of the heterogeneous source part from which they melted and ascended.
Abstract: discovered a unique type of diamond in the Tolbachik volcano frozen lava- in the Kamchatka Peninsula of far East Russia. Scientists from all over the world are quite impressed with these findings and they now classify the gemstones as completely new & unique types of diamonds. The new types of diamonds are named after the place they were found- Tolbachik Diamonds. According to geologists, the Tolbachik diamonds were born under a very peculiar natural formation where the gemstones crystalized under the direct influence of the electric discharge of lightning and the pressure from the volcanic gases. Geologists also agree that several decades ago experts wanted to create a synthetic type of diamond where the result would have been exactly the one now created naturally in the Tolbachik diamonds. In the early 60s the French wanted to create a synthetic diamond where they would use gas as primary substance and then using electric discharge for the crystallization of the gemstone. At a closer look, the Tolbachik diamonds are similar to the synthetic diamonds found on today’s market. However, the main mineralogical and geological structure of the diamond is unlike any other type of precious stone discovered until now. These diamonds are particularly large in size (200 and up to 700 microns!). According to scientists, this is actually the first time when they discovered lava rocks that show such very dense diamond content. This discovery actually gave way to very intense disputes among specialists regarding if the Lab Grown diamonds should be regarded as ‘synthetic’ any longer. The Tolbachik diamonds resemble almost in every aspect the structure of the lab grown diamonds and they are naturally formed in lava. Therefore, the Lab Grown diamonds should be more highly regarded just as the naturally mined diamonds are. Another important fact to keep in mind is that only a true expert is actually able to tell the difference between the Tolbachik diamonds created naturally and the lab grown diamonds. Someone who is not an expert would simply regard the Tolbachik diamonds as synthetic diamonds, given their different structure from the regular diamonds formed in magmatic melt. Experts found an extremely high quantity of diamonds (several hundreds of pieces) in only a small sample of frozen lava in the Kamchatka Lava in Russia. When or how these gemstones will enter the fascinating diamond industry, and if the price of jewelry featuring Tolbachik diamonds will be more budget friendly is yet to be settled…
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0609-4 14p.
Canada, Northwest Territories
deposit - Darby
Abstract: New geological and geophysical research on Canada’s Rae craton are providing an increasingly good baseline for diamond exploration. This study uses mantle xenoliths and xenocrysts from the Darby property, located ~200 km southwest of the community of Kugaaruk, Nunavut, to provide new information on the lithospheric mantle and diamond potential of the western portion of the central Rae. Peridotite xenoliths containing enough fresh olivine have a median Mg# value of 92.5, indistinguishable from the median value of 92.6 typical of cratonic peridotites world-wide. Only of the 14 peridotitic xenoliths contain fresh garnet. Of these, garnet in one sample is classified as harzburgitic (G10), giving a minimum pressure of 4.7 GPa using the P38 geobarometer (38 mW/m2 model geothermal gradient), while garnets from three peridotites are classified as lherzolitic (G9). 52 garnets picked from concentrate have lherzolitic affinities. Lherzolitic diopsides from kimberlite heavy mineral concentrate yield a lithospheric thickness of ~ 200 km. The four garnet peridotite xenoliths and 49 peridotitic garnets from concentrate yield two distinct modes in mantle sampling depths using Ni thermometry, when projected to the Cpx geotherm. A cluster of samples from the higher Ca/Cr lherzolitic garnets equilibrated at 765 to 920 °C with a group of peridotitic garnets (50 % of xenoliths and 28 % of concentrate) from the lower Ca/Cr lherzolitic garnets with anomalously high Ti concentrations yielding super-adiabatic TNi values The aluminum-in-olivine thermometer applied to olivines filtered to be “garnet facies yielded a mantle sampling portion of the mantle cargo from the diamond stability field. A suite of pyroxenitic xenoliths are a feature of each Darby kimberlite target. New screening techniques indicate that these rocks likely originate close to the crust mantle boundary. Osmium isotope analyses of the Darby peridotites reveal whole-rock Re-depletion ages ranging from Mesoarchean to Paleoproterozoic. The pyroxenite xenoliths have very radiogenic Os isotope compositions and provide the first age information from pyroxenites/“eclogites” beneath the Rae craton. Their resulting Archean whole rock TMA ages are consistent with a Mesoarchean age of the western Central Rae lithosphere older than the lithosphere beneath the Repulse Bay block in the East section of the Rae craton (Liu et al., 2016. Precambrian Research 272). The highly depleted olivine compositions, thick cold lithosphere, and Archean ages of the Darby peridotite xenoliths clearly indicate the presence of 200 km thick cold cratonic lithospheric mantle beneath the western segment of the central Rae craton circa 540 Ma. The Archean model ages of most of the pyroxenites support this, notwithstanding the fact that some of these rocks could be sampling either crust or mantle lithologies very close to the crust-mantle boundary. Mantle sampling took place well into the diamond stability field at Darby.
Mineralogy and Petrology, doi.org/10.1007/s710-018-0601-z 15p.
Africa, South Africa
deposit - Cullinan
Abstract: We studied a suite of Cullinan diamonds (<0.3 ct) with mineral inclusions, which comprised 266 Type I and 75 blank Type II (<20 ppm N) diamonds, as classified by infrared spectroscopy. More than 90% (n?=?68) of Type II diamonds do not luminesce. In contrast, 51.9% (n?=?177) of Type I diamonds luminesce, with blue colors of different intensity. Carbon isotopic compositions of Type I and II diamonds are similar, with ?13CVPDB ranging from ?2.1 to ?7.7‰for Type I diamonds (n?=?25), and from ?1.3 to ?7.8- for Type II diamonds (n?=?20). The Type II diamonds are sourced from three parageneses, lithospheric lherzolitic (45%), lithospheric eclogitic (33%), and sublithospheric mafic (22%). The lherzolitic suite contains Cr-pyrope, forsterite, enstatite, clinopyroxene and Cr-spinel formed at 1090-1530 °C and P?=?4.6-7.0 GPa. Lithospheric eclogitic diamonds containing garnet, omphacite, kyanite and coesite comprise 33% of Type II diamonds. The sublithospheric mafic paragenesis is mainly represented by Cr-free majorite, various CaSiO3 phases and omphacite equilibrated at 11.6-26 GPa, in the transition zone and the lower mantle. The lherzolitic paragenesis predominates in Type II diamonds, whereas 79% Type I diamonds are sourced from eclogites. The higher incidence of sublithospheric inclusions was found in Type II diamonds, 22% against 6% in Type I diamonds. The similarity of the mineral parageneses and C isotopic compositions in the small Cullinan Type II and Type I diamonds indicate the absence of distinct mantle processes and carbon sources for formation of studied Type II diamonds. The parent rocks and the carbon sources generally vary for Type II diamonds within a kimberlite and between kimberlites.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0607-6 16p.
Canada, Northwest Territories, South America, Brazil
deposit - Ekati, Grizzly, Kaola, Limpeza-18, Tres Ranchos-04, Kaalvallei, Samada, New Robinson
Abstract: Olivine in kimberlites can provide unique insights into magma petrogenesis, because it is the most abundant xenocrystic phase and a stable magmatic product over most of the liquid line of descent. In this study we examined the petrography and chemistry of olivine in kimberlites from different tectonic settings, including the Slave craton, Canada (Ekati: Grizzly, Koala), the Brasilia mobile belt (Limpeza-18, Tres Ranchos-04), and the Kaapvaal craton, South Africa (Kaalvallei: Samada, New Robinson). Olivine cores display a wide range of compositions (e.g., Mg#?=?78-95). The similarity in olivine composition, resorption of core zones and inclusions of mantle-derived phases, indicates that most olivine cores originated from the disaggregation of mantle peridotites, including kimberlite-metasomatised lithologies (i.e. sheared lherzolites and megacrysts). Olivine rims typically show a restricted range of Mg#, with decreasing Ni and increasing Mn and Ca contents, a characteristic of kimberlitic olivine worldwide. The rims host inclusions of groundmass minerals, which implies crystallisation just before and/or during emplacement. There is a direct correlation between olivine rim composition and groundmass mineralogy, whereby high Mg/Fe rims are associated with carbonate-rich kimberlites, and lower Mg/Fe rims are correlated with increased phlogopite and Fe-bearing oxide mineral abundances. There are no differences in olivine composition between explosive (Grizzly) and hypabyssal (Koala) kimberlites. Olivine in kimberlites also displays transitional zones and less common internal zones, between cores and rims. The diffuse transitional zones exhibit intermediate compositions between cores and rims, attributed to partial re-equilibration of xenocrystic cores with the ascending kimberlite melt. In contrast, internal zones form discrete layers with resorbed margins and restricted Mg# values, but variable Ni, Mn and Ca concentrations, which indicates a discrete crystallization event from precursor kimberlite melts at mantle depths. Overall, olivine exhibits broadly analogous zoning in kimberlites worldwide. Variable compositions for individual zones relate to different parental melt compositions rather than variations in tectonic setting or emplacement mechanism.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0607-6 16p.
Canada, Northwest Territories, South America, Brazil
deposit - Ekati, Grizzly, Kaola, Limpeza-18, Tres Ranchos-04, Kaalvallei, Samada, New Robinson
Abstract: Olivine in kimberlites can provide unique insights into magma petrogenesis, because it is the most abundant xenocrystic phase and a stable magmatic product over most of the liquid line of descent. In this study we examined the petrography and chemistry of olivine in kimberlites from different tectonic settings, including the Slave craton, Canada (Ekati: Grizzly, Koala), the Brasilia mobile belt (Limpeza-18, Tres Ranchos-04), and the Kaapvaal craton, South Africa (Kaalvallei: Samada, New Robinson). Olivine cores display a wide range of compositions (e.g., Mg#?=?78-95). The similarity in olivine composition, resorption of core zones and inclusions of mantle-derived phases, indicates that most olivine cores originated from the disaggregation of mantle peridotites, including kimberlite-metasomatised lithologies (i.e. sheared lherzolites and megacrysts). Olivine rims typically show a restricted range of Mg#, with decreasing Ni and increasing Mn and Ca contents, a characteristic of kimberlitic olivine worldwide. The rims host inclusions of groundmass minerals, which implies crystallisation just before and/or during emplacement. There is a direct correlation between olivine rim composition and groundmass mineralogy, whereby high Mg/Fe rims are associated with carbonate-rich kimberlites, and lower Mg/Fe rims are correlated with increased phlogopite and Fe-bearing oxide mineral abundances. There are no differences in olivine composition between explosive (Grizzly) and hypabyssal (Koala) kimberlites. Olivine in kimberlites also displays transitional zones and less common internal zones, between cores and rims. The diffuse transitional zones exhibit intermediate compositions between cores and rims, attributed to partial re-equilibration of xenocrystic cores with the ascending kimberlite melt. In contrast, internal zones form discrete layers with resorbed margins and restricted Mg# values, but variable Ni, Mn and Ca concentrations, which indicates a discrete crystallization event from precursor kimberlite melts at mantle depths. Overall, olivine exhibits broadly analogous zoning in kimberlites worldwide. Variable compositions for individual zones relate to different parental melt compositions rather than variations in tectonic setting or emplacement mechanism.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0607-6 16p.
Canada, Northwest Territories, South America, Brazil
deposit - Ekati, Grizzly, Kaola, Limpeza-18, Tres Ranchos-04, Kaalvallei, Samada, New Robinson
Abstract: Olivine in kimberlites can provide unique insights into magma petrogenesis, because it is the most abundant xenocrystic phase and a stable magmatic product over most of the liquid line of descent. In this study we examined the petrography and chemistry of olivine in kimberlites from different tectonic settings, including the Slave craton, Canada (Ekati: Grizzly, Koala), the Brasilia mobile belt (Limpeza-18, Tres Ranchos-04), and the Kaapvaal craton, South Africa (Kaalvallei: Samada, New Robinson). Olivine cores display a wide range of compositions (e.g., Mg#?=?78-95). The similarity in olivine composition, resorption of core zones and inclusions of mantle-derived phases, indicates that most olivine cores originated from the disaggregation of mantle peridotites, including kimberlite-metasomatised lithologies (i.e. sheared lherzolites and megacrysts). Olivine rims typically show a restricted range of Mg#, with decreasing Ni and increasing Mn and Ca contents, a characteristic of kimberlitic olivine worldwide. The rims host inclusions of groundmass minerals, which implies crystallisation just before and/or during emplacement. There is a direct correlation between olivine rim composition and groundmass mineralogy, whereby high Mg/Fe rims are associated with carbonate-rich kimberlites, and lower Mg/Fe rims are correlated with increased phlogopite and Fe-bearing oxide mineral abundances. There are no differences in olivine composition between explosive (Grizzly) and hypabyssal (Koala) kimberlites. Olivine in kimberlites also displays transitional zones and less common internal zones, between cores and rims. The diffuse transitional zones exhibit intermediate compositions between cores and rims, attributed to partial re-equilibration of xenocrystic cores with the ascending kimberlite melt. In contrast, internal zones form discrete layers with resorbed margins and restricted Mg# values, but variable Ni, Mn and Ca concentrations, which indicates a discrete crystallization event from precursor kimberlite melts at mantle depths. Overall, olivine exhibits broadly analogous zoning in kimberlites worldwide. Variable compositions for individual zones relate to different parental melt compositions rather than variations in tectonic setting or emplacement mechanism.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0607-6 16p.
Canada, Northwest Territories, South America, Brazil
deposit - Ekati, Grizzly, Kaola, Limpeza-18, Tres Ranchos-04, Kaalvallei, Samada, New Robinson
Abstract: Olivine in kimberlites can provide unique insights into magma petrogenesis, because it is the most abundant xenocrystic phase and a stable magmatic product over most of the liquid line of descent. In this study we examined the petrography and chemistry of olivine in kimberlites from different tectonic settings, including the Slave craton, Canada (Ekati: Grizzly, Koala), the Brasilia mobile belt (Limpeza-18, Tres Ranchos-04), and the Kaapvaal craton, South Africa (Kaalvallei: Samada, New Robinson). Olivine cores display a wide range of compositions (e.g., Mg#?=?78-95). The similarity in olivine composition, resorption of core zones and inclusions of mantle-derived phases, indicates that most olivine cores originated from the disaggregation of mantle peridotites, including kimberlite-metasomatised lithologies (i.e. sheared lherzolites and megacrysts). Olivine rims typically show a restricted range of Mg#, with decreasing Ni and increasing Mn and Ca contents, a characteristic of kimberlitic olivine worldwide. The rims host inclusions of groundmass minerals, which implies crystallisation just before and/or during emplacement. There is a direct correlation between olivine rim composition and groundmass mineralogy, whereby high Mg/Fe rims are associated with carbonate-rich kimberlites, and lower Mg/Fe rims are correlated with increased phlogopite and Fe-bearing oxide mineral abundances. There are no differences in olivine composition between explosive (Grizzly) and hypabyssal (Koala) kimberlites. Olivine in kimberlites also displays transitional zones and less common internal zones, between cores and rims. The diffuse transitional zones exhibit intermediate compositions between cores and rims, attributed to partial re-equilibration of xenocrystic cores with the ascending kimberlite melt. In contrast, internal zones form discrete layers with resorbed margins and restricted Mg# values, but variable Ni, Mn and Ca concentrations, which indicates a discrete crystallization event from precursor kimberlite melts at mantle depths. Overall, olivine exhibits broadly analogous zoning in kimberlites worldwide. Variable compositions for individual zones relate to different parental melt compositions rather than variations in tectonic setting or emplacement mechanism.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0607-6 16p.
Canada, Northwest Territories, South America, Brazil
deposit - Ekati, Grizzly, Kaola, Limpeza-18, Tres Ranchos-04, Kaalvallei, Samada, New Robinson
Abstract: Olivine in kimberlites can provide unique insights into magma petrogenesis, because it is the most abundant xenocrystic phase and a stable magmatic product over most of the liquid line of descent. In this study we examined the petrography and chemistry of olivine in kimberlites from different tectonic settings, including the Slave craton, Canada (Ekati: Grizzly, Koala), the Brasilia mobile belt (Limpeza-18, Tres Ranchos-04), and the Kaapvaal craton, South Africa (Kaalvallei: Samada, New Robinson). Olivine cores display a wide range of compositions (e.g., Mg#?=?78-95). The similarity in olivine composition, resorption of core zones and inclusions of mantle-derived phases, indicates that most olivine cores originated from the disaggregation of mantle peridotites, including kimberlite-metasomatised lithologies (i.e. sheared lherzolites and megacrysts). Olivine rims typically show a restricted range of Mg#, with decreasing Ni and increasing Mn and Ca contents, a characteristic of kimberlitic olivine worldwide. The rims host inclusions of groundmass minerals, which implies crystallisation just before and/or during emplacement. There is a direct correlation between olivine rim composition and groundmass mineralogy, whereby high Mg/Fe rims are associated with carbonate-rich kimberlites, and lower Mg/Fe rims are correlated with increased phlogopite and Fe-bearing oxide mineral abundances. There are no differences in olivine composition between explosive (Grizzly) and hypabyssal (Koala) kimberlites. Olivine in kimberlites also displays transitional zones and less common internal zones, between cores and rims. The diffuse transitional zones exhibit intermediate compositions between cores and rims, attributed to partial re-equilibration of xenocrystic cores with the ascending kimberlite melt. In contrast, internal zones form discrete layers with resorbed margins and restricted Mg# values, but variable Ni, Mn and Ca concentrations, which indicates a discrete crystallization event from precursor kimberlite melts at mantle depths. Overall, olivine exhibits broadly analogous zoning in kimberlites worldwide. Variable compositions for individual zones relate to different parental melt compositions rather than variations in tectonic setting or emplacement mechanism.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0607-6 16p.
Canada, Northwest Territories, South America, Brazil
deposit - Ekati, Grizzly, Kaola, Limpeza-18, Tres Ranchos-04, Kaalvallei, Samada, New Robinson
Abstract: Olivine in kimberlites can provide unique insights into magma petrogenesis, because it is the most abundant xenocrystic phase and a stable magmatic product over most of the liquid line of descent. In this study we examined the petrography and chemistry of olivine in kimberlites from different tectonic settings, including the Slave craton, Canada (Ekati: Grizzly, Koala), the Brasilia mobile belt (Limpeza-18, Tres Ranchos-04), and the Kaapvaal craton, South Africa (Kaalvallei: Samada, New Robinson). Olivine cores display a wide range of compositions (e.g., Mg#?=?78-95). The similarity in olivine composition, resorption of core zones and inclusions of mantle-derived phases, indicates that most olivine cores originated from the disaggregation of mantle peridotites, including kimberlite-metasomatised lithologies (i.e. sheared lherzolites and megacrysts). Olivine rims typically show a restricted range of Mg#, with decreasing Ni and increasing Mn and Ca contents, a characteristic of kimberlitic olivine worldwide. The rims host inclusions of groundmass minerals, which implies crystallisation just before and/or during emplacement. There is a direct correlation between olivine rim composition and groundmass mineralogy, whereby high Mg/Fe rims are associated with carbonate-rich kimberlites, and lower Mg/Fe rims are correlated with increased phlogopite and Fe-bearing oxide mineral abundances. There are no differences in olivine composition between explosive (Grizzly) and hypabyssal (Koala) kimberlites. Olivine in kimberlites also displays transitional zones and less common internal zones, between cores and rims. The diffuse transitional zones exhibit intermediate compositions between cores and rims, attributed to partial re-equilibration of xenocrystic cores with the ascending kimberlite melt. In contrast, internal zones form discrete layers with resorbed margins and restricted Mg# values, but variable Ni, Mn and Ca concentrations, which indicates a discrete crystallization event from precursor kimberlite melts at mantle depths. Overall, olivine exhibits broadly analogous zoning in kimberlites worldwide. Variable compositions for individual zones relate to different parental melt compositions rather than variations in tectonic setting or emplacement mechanism.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0607-6 16p.
Canada, Northwest Territories, South America, Brazil
deposit - Ekati, Grizzly, Kaola, Limpeza-18, Tres Ranchos-04, Kaalvallei, Samada, New Robinson
Abstract: Olivine in kimberlites can provide unique insights into magma petrogenesis, because it is the most abundant xenocrystic phase and a stable magmatic product over most of the liquid line of descent. In this study we examined the petrography and chemistry of olivine in kimberlites from different tectonic settings, including the Slave craton, Canada (Ekati: Grizzly, Koala), the Brasilia mobile belt (Limpeza-18, Tres Ranchos-04), and the Kaapvaal craton, South Africa (Kaalvallei: Samada, New Robinson). Olivine cores display a wide range of compositions (e.g., Mg#?=?78-95). The similarity in olivine composition, resorption of core zones and inclusions of mantle-derived phases, indicates that most olivine cores originated from the disaggregation of mantle peridotites, including kimberlite-metasomatised lithologies (i.e. sheared lherzolites and megacrysts). Olivine rims typically show a restricted range of Mg#, with decreasing Ni and increasing Mn and Ca contents, a characteristic of kimberlitic olivine worldwide. The rims host inclusions of groundmass minerals, which implies crystallisation just before and/or during emplacement. There is a direct correlation between olivine rim composition and groundmass mineralogy, whereby high Mg/Fe rims are associated with carbonate-rich kimberlites, and lower Mg/Fe rims are correlated with increased phlogopite and Fe-bearing oxide mineral abundances. There are no differences in olivine composition between explosive (Grizzly) and hypabyssal (Koala) kimberlites. Olivine in kimberlites also displays transitional zones and less common internal zones, between cores and rims. The diffuse transitional zones exhibit intermediate compositions between cores and rims, attributed to partial re-equilibration of xenocrystic cores with the ascending kimberlite melt. In contrast, internal zones form discrete layers with resorbed margins and restricted Mg# values, but variable Ni, Mn and Ca concentrations, which indicates a discrete crystallization event from precursor kimberlite melts at mantle depths. Overall, olivine exhibits broadly analogous zoning in kimberlites worldwide. Variable compositions for individual zones relate to different parental melt compositions rather than variations in tectonic setting or emplacement mechanism.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0607-6 16p.
Canada, Northwest Territories, South America, Brazil
deposit - Ekati, Grizzly, Kaola, Limpeza-18, Tres Ranchos-04, Kaalvallei, Samada, New Robinson
Abstract: Olivine in kimberlites can provide unique insights into magma petrogenesis, because it is the most abundant xenocrystic phase and a stable magmatic product over most of the liquid line of descent. In this study we examined the petrography and chemistry of olivine in kimberlites from different tectonic settings, including the Slave craton, Canada (Ekati: Grizzly, Koala), the Brasilia mobile belt (Limpeza-18, Tres Ranchos-04), and the Kaapvaal craton, South Africa (Kaalvallei: Samada, New Robinson). Olivine cores display a wide range of compositions (e.g., Mg#?=?78-95). The similarity in olivine composition, resorption of core zones and inclusions of mantle-derived phases, indicates that most olivine cores originated from the disaggregation of mantle peridotites, including kimberlite-metasomatised lithologies (i.e. sheared lherzolites and megacrysts). Olivine rims typically show a restricted range of Mg#, with decreasing Ni and increasing Mn and Ca contents, a characteristic of kimberlitic olivine worldwide. The rims host inclusions of groundmass minerals, which implies crystallisation just before and/or during emplacement. There is a direct correlation between olivine rim composition and groundmass mineralogy, whereby high Mg/Fe rims are associated with carbonate-rich kimberlites, and lower Mg/Fe rims are correlated with increased phlogopite and Fe-bearing oxide mineral abundances. There are no differences in olivine composition between explosive (Grizzly) and hypabyssal (Koala) kimberlites. Olivine in kimberlites also displays transitional zones and less common internal zones, between cores and rims. The diffuse transitional zones exhibit intermediate compositions between cores and rims, attributed to partial re-equilibration of xenocrystic cores with the ascending kimberlite melt. In contrast, internal zones form discrete layers with resorbed margins and restricted Mg# values, but variable Ni, Mn and Ca concentrations, which indicates a discrete crystallization event from precursor kimberlite melts at mantle depths. Overall, olivine exhibits broadly analogous zoning in kimberlites worldwide. Variable compositions for individual zones relate to different parental melt compositions rather than variations in tectonic setting or emplacement mechanism.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0604-9 12p.
Africa, Botswana
deposit - Karowe
Abstract: Mineral inclusions in diamonds play a critical role in constraining the relationship between diamonds and mantle lithologies. Here we report the first major and trace element study of mineral inclusions in diamonds from the Karowe Mine in north-east Botswana, along the western edge of the Zimbabwe Craton. From a total of 107 diamonds, 134 silicate, 15 oxide, and 22 sulphide inclusions were recovered. The results reveal that 53% of Karowe inclusion-bearing diamonds derived from eclogitic sources, 44% are peridotitic, 2% have a sublithospheric origin, and 1% are websteritic. The dominant eclogitic diamond substrates sampled at Karowe are compositionally heterogeneous, as reflected in wide ranges in the CaO contents (4-16 wt%) of garnets and the Mg# (69-92) and jadeite contents (14-48 mol%) of clinopyroxenes. Calculated bulk rock REEN patterns indicate that both shallow and deep levels of the subducted slab(s) were sampled, including cumulate-like protoliths. Peridotitic garnet compositions largely derive from harzburgite/dunite substrates (~90%), with almost half the garnets having CaO contents <1.8 wt%, consistent with pyroxene-free (dunitic) sources. The highly depleted character of the peridotitic diamond substrates is further documented by the high mean and median Mg# (93.1) of olivine inclusions. One low-Ca garnet records a very high Cr2O3 content (14.7 wt%), implying that highly depleted cratonic lithosphere at the time of diamond formation extended to at least 220 km depth. Inclusion geothermobarometry indicates that the formation of peridotitic diamonds occurred along a 39-40 mW/m2 model geotherm. A sublithospheric inclusion suite is established by three eclogitic garnets containing a majorite component, a feature so far unique within the Orapa cluster. These low- and high-Ca majoritic garnets follow pyroxenitic and eclogitic trends of majoritic substitution, respectively. The origin of the majorite-bearing diamonds is estimated to be between 330 to 420 km depth, straddling the asthenosphere-transition zone boundary. This new observation of superdeep mineral inclusions in Karowe diamonds is consistent with a sublithospheric origin for the exceptionally large diamonds from this mine.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0614-7 12p.
Canada, Quebec
deposit - Renard
Abstract: The Renard 2 pipe is currently the deepest-drilled and most extensively studied kimberlite body in the Renard cluster, central Québec, Canada, forming the major component of the Mineral Resource of Stornoway Diamond Corporation’s Renard Mine. Renard 2 is infilled with two distinct kimberlite units that exhibit Kimberley-type pyroclastic kimberlite and related textures. Hypabyssal kimberlite also occurs as smaller cross-cutting sheets and irregular intrusions. The units are distinguished by their rock textures, groundmass mineral assemblages, olivine macrocryst size distributions and replacement products, mantle and country rock xenolith contents, whole rock geochemical signatures, bulk densities and diamond grades. These differences are interpreted to reflect different mantle ascent and near-surface emplacement processes and are here demonstrated to be vertically continuous from present surface to over 1000 m depth. The distinctive petrological features together with sharp, steep and cross-cutting internal contact relationships, show that each unit was formed from a separate batch of mantle-derived kimberlite magma, and was completely solidified before subsequent emplacement of the later unit. The mineralogy and textures of the ultra-fine-grained interclast matrix are consistent with those described at numerous Kimberley-type pyroclastic kimberlite localities around the world and are interpreted to reflect rapid primary crystallization during emplacement of separate kimberlite magmatic systems. The units of fractured and brecciated country rock surrounding the main kimberlite pipe contain kimberlite-derived material including carbonate providing evidence of subsurface brecciation. Together these data show that Renard 2 represents the deeper parts of a Kimberley-type pyroclastic kimberlite pipe system and demonstrates that their diagnostic features result from magmatic crystallisation during subsurface volcanic emplacement processes.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0620-9 11p.
Africa, Sierra Leone
deposit - Koidu
Abstract: This paper documents the application of a microdiamond-based approach to the estimation of diamond grade in the Pipe 1 kimberlite at the Koidu mine in Sierra Leone. A geological model of Pipe 1 was constructed to represent the distribution and volume of the dominant kimberlite units within the pipe. Bulk samples, along with representative microdiamond samples, were collected from these units at surface and were used to define the ratio between microdiamond stone frequency (+212 ?m stones per kilogram) and recoverable macrodiamond grade (+1.2 mm carats per tonne; 1 carat?=?0.2 g). These ratios were applied to a comprehensive, spatially representative microdiamond sample dataset and were combined with a spatial model of country-rock xenolith dilution within the pipe to estimate +1.2 mm recoverable grades. The resource estimate was reconciled with subsequent production results in the elevation range 160 to 100 m above sea level. Production results for each of the six 10 m benches covering this elevation range were compared to the estimated average grades for these zones in the pipe. For the five cases where most of the kimberlite mass on a given bench is represented in the production data, the results show a maximum discrepancy of 6% between predicted and reported production grade with no indication of any consistent bias. This indicates that, when supported by a sound geological model and suitable microdiamond and macrodiamond data, the microdiamond-based estimation approach can provide reliable constraints on macrodiamond grade, even in the case of geologically complex bodies such as Koidu Pipe 1.
Abstract: Trends in concentration of selected trace elements in residual soils on four known diamondiferous kimberlite pipes (3, 4, 8 and 9) occurring at Lattavaram within the Wajrakarur Kimberlite Field (WKF) is attempted for the first time. The pipes 3 and 4 are exposed whereas the 8 and 9 are concealed under calcrete and colluvium. For this purpose, elements like Nb, Cr, Ni, Co, Zr, Mg, Sr and La are used to understand their concentrations in the kimberlitic soils in comparison with background granitic soils. It is observed that the soils on kimberlite pipes show conspicuous enrichment of elements such as Cr, Co, Nb, Ni, Mg and Sr when compared to soils in the country rock granitoid. However, no much variation in the elements La and Zr patterns between the kimberlitic and background soils is noticed. The high pulse in trace elements in kimberlitic soils is attributed to the presence of primary kimberlitic minerals and their weathered products in the soil. This particular aspect of pedogeochemistry is envisaged to be useful as an exploration tool in search of kimberlites in cratonic parts of southern India. An enrichment of Nb content upto 45 ppm in residual soils may be considered as anamolous in the craonic parts of Indian subcontinent, which needs to be confirmed and taken forward in conjunction with high resolution geological mapping, geophysics followed up by drilling for confirmation of kimberlite/lamproite occurrence.
Abstract: The Zarnitsa kimberlite pipe is one of the largest pipes of the Yakutian diamondiferous province. Currently, some limited published data exists on the diamonds from this deposit. Among the diamond population of this pipe there is a specific series of dark gray to black diamonds with transition morphologies between octahedron and rounded rhombic dodecahedron. These diamonds have specific zonal and sectorial mosaic-block internal structures. The inner parts of these crystals have polycrystalline structure with significant misorientations between sub-individuals. The high consistency of the mechanical admixtures (inclusions) in the diamonds cores can cause a high grid stress of the crystal structure and promote the block (polycrystalline) structure of the core components. These diamond crystals have subsequently been formed due to crystallization of bigger sub-individuals on the polycrystalline cores according to the geometric selection law.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0624-5 12p.
Africa, Lesotho
deposit - Liqhobong
Abstract: The Cretaceous Liqhobong kimberlite cluster comprises at least six known diamondiferous Group 1 kimberlite bodies; namely the circular Main Pipe (8.5 ha), ovoid Satellite Pipe (1.6 ha), Discovery Blow (0.15 ha), Blow (0.1 ha), the Main Dike adjoining the blows and pipes, and one other recently exposed dike. The kimberlites intrude Jurassic Drakensberg lavas and outcrop at ~2650 masl in rugged Maluti Mountain terrain, and are emplaced along a strike of about 2.5km. The cluster represents at least three episodes of structurally controlled kimberlite intrusion; the first which comprised the dike(s?) and the two blows (the blows being dike enlargements emplaced 1km apart) and later the two separate emplacements of the Main and Satellite Pipes.
Geochimica et Cosmochimica Acta, Vol. 232, pp. 303-328.
Mantle
deposit - Ronda, Beni Bousera
Abstract: We present an integrated geochemical study of ultra-high pressure (UHP) garnet pyroxenites from the Ronda and Beni Bousera peridotite massifs (Betic-Rif Belt, westernmost Mediterranean). Based on their Sr-Nd-Pb-Hf isotopic systematics, we classify UHP garnet pyroxenites into three groups: Group A pyroxenites (Al2O3: 15-17.5?wt.%) have low initial 87Sr/86Sr, relatively high ?Nd, ?Hf and 206Pb/204Pb ratios, and variable 207Pb/204Pb and 208Pb/204Pb. Group B pyroxenites (Al2O3?
Geochimica et Cosmochimica Acta, Vol. 232, pp. 303-328.
Mantle
deposit - Ronda, Beni Bousera
Abstract: We present an integrated geochemical study of ultra-high pressure (UHP) garnet pyroxenites from the Ronda and Beni Bousera peridotite massifs (Betic-Rif Belt, westernmost Mediterranean). Based on their Sr-Nd-Pb-Hf isotopic systematics, we classify UHP garnet pyroxenites into three groups: Group A pyroxenites (Al2O3: 15-17.5?wt.%) have low initial 87Sr/86Sr, relatively high ?Nd, ?Hf and 206Pb/204Pb ratios, and variable 207Pb/204Pb and 208Pb/204Pb. Group B pyroxenites (Al2O3?
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0613-8 19p.
Africa, South Africa
deposit - Finsch
Abstract: Microinclusion-bearing diamonds offer the opportunity to investigate relationships between mantle metasomatism, diamond formation and kimberlite eruptions in intracratonic provinces. We have analyzed a suite of 7 microinclusion-bearing diamonds from the Finsch Group II kimberlite, South Africa, and identified two diamond populations: ‘Finsch IaA’ diamonds have nitrogen solely in A-centers and contain saline high-density-fluid (HDF) microinclusions, while ‘Finsch IaAB’ diamonds have nitrogen in both A- and B-centers (25-35% B-centers) and are characterized by carbonatite HDF compositions. Based on nitrogen aggregation states and estimates for mantle residence temperatures, we conclude that ‘Finsch IaA’ diamonds formed during a young saline metasomatic event that preceded kimberlite eruption by ~50 kyr to 15 Myr. The possible timing of metasomatism and formation of ‘Finsch IaAB’ diamonds by carbonatite HDFs is less constrained, and could have taken place between ~15 Myr and 2 Gyr before eruption. Two of the diamonds encapsulated omphacite microinclusions in association with saline or low-Mg carbonatitic-like HDF. We observe compositional differences for Al2O3 vs. CaO between these metasomatised omphacites, and also compared to omphacites in mantle eclogites which were identified as metasomatised by kimberlite or high-Mg carbonatite; suggesting a possible relationship between Al2O3 and CaO in metasomatised omphacite and the type of fluid/melt it interacted with. The combined data for microinclusion-bearing diamonds from the Finsch Group II kimberlite and the neighbouring Group I kimberlites at Koffiefontein and De Beers Pool indicate that a substantial volume of the southwest Kaapvaal deep lithosphere was impacted by saline metasomatism during Cretaceous time, and a direct relationship between saline metasomatism, diamond formation and the Kaapvaal late-Mesozoic ‘kimberlite bloom’. We therefore conclude that saline HDFs play a key role in the buildup of metasomatic mantle sources leading to kimberlite eruptions.
Mineralogical Magazine, Vol. 82, no. 2, pp. 329-346.
Russia, Kola Peninsula
deposit - Kovdor
Abstract: Two quintinite polytypes, 3R and 2T, which are new for the Kovdor alkaline-ultrabasic complex, have been structurally characterized. The crystal structure of quintinite-2T was solved by direct methods and refined to R1 = 0.048 on the basis of 330 unique reflections. The structure is trigonal, P c1, a = 5.2720(6), c = 15.113(3) Å and V = 363.76(8) Å3. The crystal structure consists of [Mg2Al(OH)6]+ brucite-type layers with an ordered distribution of Mg2+ and Al3+ cations according to the × superstructure with the layers stacked according to a hexagonal type. The complete layer stacking sequence can be described as …=Ab1C = Cb1A=…. The crystal structure of quintinite-3R was solved by direct methods and refined to R1 = 0.022 on the basis of 140 unique reflections. It is trigonal, R m, a = 3.063(1), c = 22.674(9) Å and V = 184.2(1) Å3. The crystal structure is based upon double hydroxide layers [M2+,3+(OH)2] with disordered distribution of Mg, Al and Fe and with the layers stacked according to a rhombohedral type. The stacking sequence of layers can be expressed as …=?B = BC = CA=… The study of morphologically different quintinite generations grown on one another detected the following natural sequence of polytype formation: 2H ? 2T ? 1M that can be attributed to a decrease of temperature during crystallization. According to the information-based approach to structural complexity, this sequence corresponds to the increasing structural information per atom (IG): 1.522 ? 1.706 ? 2.440 bits, respectively. As the IG value contributes negatively to the configurational entropy of crystalline solids, the evolution of polytypic modifications during crystallization corresponds to the decreasing configurational entropy. This is in agreement with the general principle that decreasing temperature corresponds to the appearance of more complex structures.
Geochimica et Cosmochimica Acta, Vol. 213, 1, pp. 574-592.
Africa, Botswana
deposit - Orapa
Abstract: Major- and trace-element compositions of garnet and clinopyroxene, as well as 87Sr/86Sr in clinopyroxene and ?18O in garnet in eclogite and pyroxenite xenoliths from Orapa, at the western margin of the Zimbabwe craton (central Botswana), were investigated in order to trace their origin and evolution in the mantle lithosphere. Two groups of eclogites are distinguished with respect to 87Sr/86Sr: One with moderate ratios (0.7026-0.7046) and another with 87Sr/86Sr >0.7048 to 0.7091. In the former group, heavy ?18O attests to low-temperature alteration on the ocean floor, while 87Sr/86Sr correlates with indices of low-pressure igneous processes (Eu/Eu?, Mg#, Sr/Y). This suggests relatively undisturbed long-term ingrowth of 87Sr at near-igneous Rb/Sr after metamorphism, despite the exposed craton margin setting. The high-87Sr/86Sr group has mainly mantle-like ?18O and is suggested to have interacted with a small-volume melt derived from an aged phlogopite-rich metasome. The overlap of diamondiferous and graphite-bearing eclogites and pyroxenites over a pressure interval of ?3.2 to 4.9 GPa is interpreted as reflecting a mantle parcel beneath Orapa that has moved out of the diamond stability field, due to a change in geotherm and/or decompression. Diamondiferous eclogites record lower median 87Sr/86Sr (0.7039) than graphite-bearing samples (0.7064) and carbon-free samples (0.7051), suggesting that interaction with the - possibly oxidising - metasome-derived melt caused carbon removal in some eclogites, while catalysing the conversion of diamond to graphite in others. This highlights the role of small-volume melts in modulating the lithospheric carbon cycle. Compared to diamondiferous eclogites, eclogitic inclusions in diamonds are restricted to high FeO and low SiO2, CaO and Na2O contents, they record higher equilibrium temperatures and garnets have mostly mantle-like O isotopic composition. We suggest that this signature was imparted by a sublithospheric melt with contributions from a clinopyroxene-rich source, possibly related to the ca. 2.0 Ga Bushveld event.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0621-8 16p.
Canada, Northwest Territories
deposit - Kelvin, Faraday
Abstract: The Kennady North Project kimberlites (Northwest Territories of Canada) comprises multiple shallow dipping dykes and several volcaniclastic bodies that have an unusual shallow plunging geometry and complex "pipe" shapes that are termed chonoliths. The detailed exploration of the entire system provides exceptional evidence for subterranean volcanic conduit growth processes. The possible processes leading to the development of the kimberlite bodies are discussed, with emphasis on the importance of the subsurface intrusive system geometry and the local stress tensor. Emplacement into a locally compressive stress regime (i.e. ?1 and ?2 inclined at a low angle to surface) could change the kimberlite emplacement geometries to that observed at Kennady North. Models are proposed for the development of the chonoliths, to emphasize aspects of the growth of kimberlite systems that are not well understood. The conclusions challenge or evolve current emplacement models and should influence kimberlite exploration and resource definition assumptions.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0621-8 16p.
Canada, Northwest Territories
deposit - Kelvin, Faraday
Abstract: The Kennady North Project kimberlites (Northwest Territories of Canada) comprises multiple shallow dipping dykes and several volcaniclastic bodies that have an unusual shallow plunging geometry and complex "pipe" shapes that are termed chonoliths. The detailed exploration of the entire system provides exceptional evidence for subterranean volcanic conduit growth processes. The possible processes leading to the development of the kimberlite bodies are discussed, with emphasis on the importance of the subsurface intrusive system geometry and the local stress tensor. Emplacement into a locally compressive stress regime (i.e. ?1 and ?2 inclined at a low angle to surface) could change the kimberlite emplacement geometries to that observed at Kennady North. Models are proposed for the development of the chonoliths, to emphasize aspects of the growth of kimberlite systems that are not well understood. The conclusions challenge or evolve current emplacement models and should influence kimberlite exploration and resource definition assumptions.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Journal of Volcanology and Seismology, Vol. 12, 2, pp. 140-149.
Russia
deposit- Nyurbinskaya
Abstract: The study of viscosity in sub-liquidus heterogeneous media, which includes kimberlite magma at the pressures and temperatures that prevail in the mantle, is an urgent task. We have conducted experiments in the serpentine-olivine, serpentine-CaCO3?olivine, and native kimberlite-olivine systems at a pressure of 4 GPa and temperatures of 1400?1600°? in a BARS high-pressure device using the technique of a falling Pt pellet. The samples were examined after experiments to find fine-grained chilled mass of crystals where the Pt pellet was observed at the time of chilling. The concentration of the solid phase was varied in the experiments between 10 and 50 wt %. We showed that when 50 wt % of olivine grains has been introduced, it was not possible to detect the motion of the Pt pellet, while when the concentration of olivine xenocrysts reached 10 wt %, the Pt pellet very rapidly descended to the bottom of the reaction volume. Viscosity was calculated using the Stokes method. We found that the viscosity of a homogeneous kimberlite melt at 4 GPa and 1600°? is below 2 Pa s, with the viscosity of a melt that contained up to 10 wt % of the solid phase being approximately constant. A kimberlite melt that contained 30 wt % of the solid phase had a viscosity on the order of 100 Pa s, while with 50 wt % of the solid phase the relative viscosity of an ultrabasic system increased to reach values over 1000 Pa s.
Abstract: We present the joint interpretation of airborne electromagnetic and aeromagnetic data, acquired to study kimberlite pipes. We analyse the data surveyed in 2005 over Drybones Bay, Archean Slave Province of the Northwest Territories, northern Canada. This area hosts a recently discovered kimberlite province with >150 kimberlite pipes. Magnetic and electromagnetic data were each one modelled by 1D inversion. For magnetic data we inverted vertical soundings built through upward continuations of the measured data at various altitudes. The validity of the method was prior verified by tests on synthetic data. Electromagnetic data were processed and inverted using the modified AarhusINV code, with Cole-Cole modelling, in order to take into account induced polarization effects, consisting in negative voltages and otherwise skewed transients. The integrated study of the two kinds of data has led to a better understanding of the structures at depth, even though the comparison between the magnetic and the electromagnetic models shows the different sensitivity of the two methods with respect to the geological structure at Drybones Bay.
Abstract: We report preliminary results of a systematic search for fluid/melt microinclusions in mantle minerals. “Dusty” garnets from xenolith XRV6 [1], a heavily metasomatised Type I eclogite from Roberts Victor mine, SA, carry many microinclusions (<1 ?m). FTIR analyses of "dusty" zones indicate the presence of molecular water in the inclusions and hydroxyl groups in the garnet. EPMA analysis of 136 microinclusions constrains the bulk composition of the microinclusions. Compared to the host garnet, they are enriched in TiO2, FeO, CaO, Na2O and K2O and depleted in Al2O3 and MgO. The silica contents seem to be similar to that of the host garnet. Figure 1: a. Backscatter image of the microinclusions in XRV6 garnet. b. K2O vs. MgO of the clear garnet (red) and the microinclusions (+ their surrounding garnet, blue). Most of the elements form compositional mixing arrays of microinclusion+garnet (Fig. 1b). The arrays trend away from the compositions of large melt pools or secondary minerals found in the xenolith. They point towards the array of silicic to low-Mg carbonatitic high density fluids (HDFs) trapped in diamonds, indicating the role of such fluids in mantle metasomatism.
Abstract: Roots of continental cratons keep a long record of multiple metasomatic events, but their trace is complicated due to the mixed signals left by these events in the composition of mantle silicate minerals. Simple composition helps diamonds to provide a more robust record of the latest metasomatic events which they witnessed. Growth and dissolution features on the diamond surface are sensitive to the composition of the reacting media. In this study we use mantle-derived resorption features on natural diamonds to examine the nature of metasomatic events in diamondiferous mantle lithologies. We use experiments at mantle conditions to examine how the composition of fluids and melts affect diamond resorption. We then compare these results to the features of natural diamonds to determine which of the tested compositions could have acted as metasomatic agents in Earth’s cratonic roots. Diamond dissolution experiments conducted at 6 GPa, 1200 - 1500oC using synthetic MgO-CaO-SiO2-CO2-H2O system examined the effect of CHO fluid, silica-saturated CHO fluid, aqueous and “dry” silica-carbonate and carbonate melts. Results show that the main control of diamond resorption morphology is the state of the reacting media: fluid vs. melt. We compared the experimental results to diamonds with mantle-derived resorption features from two kimberlites from the Orapa kimberlite cluster (Botswana). We identified twelve mantle-derived resorption types, none of which resembled the products of resorption in fluids. Most of the observed resorption types could be produced by dissolution in mantle melts with variable proportions of carbonate and silicate components and in the range of temperatures. The most abundant resorption type resembles the product of diamond dissolution in carbonate melts at temperatures above 1450oC. Our results suggest that fluid-metasomatism is not destructive for diamonds while melt-metasomatism is. The lower hydrous carbonated solidus of lherzolite compared to harzburgite can result in the shift the process from diamond growth in fluids to diamond dissolution in melts due to metasomatic transformation of harzburgite into lherzolite.
deposit - Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya, Venetia, Wawa, Diavik
Abstract: Earth’s mantle is by far the largest silicate-hosted reservoir of carbon. Diamonds are unrivalled in their ability to record the cycle of mantle carbon and other volatiles over a vast portion of the Earth’s history. They are the product of ascending, cooling, carbon-saturated, metasomatic fluidsmelts and/or redox reactions, predominantly within peridotitic and eclogitic domains in the mantle lithosphere. This paper reports the results of a major secondary ion mass spectrometry (SIMS) carbon isotope study, carried out on 127 diamond samples, spanning a large range of geological time. Detailed transects across the incremental growth zones within each diamond were measured for C isotopes, N abundances and, for samples with N >~200 at.ppm, N isotopes. Given that all of the samples are fragments, recovered when the original crystals were broken to liberate their inclusions, 81 of the analytical traverses have confirmed growth direction context. 98 samples are from studies that have confirmed the dates of the individual diamonds through analysis of their silicate or sulphide inclusions, from source localities including Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya & Venetia. Additional samples come from Wawa (a minimum age) and Diavik where the samples are tied via inclusion paragenesis to published ages. The peridotitic dataset covers the age range of ~3.3 - 2.0 Ga, with the eclogitic data from 2.9 - 1.0 Ga. In total, 751 carbon isotope and nitrogen concentration measurements have been obtained (425 on peridotitic diamonds, and 326 on eclogitic diamonds) with 470 nitrogen isotope measurements (190 P, 280 E). We attempt to constrain the diamond carbon isotope record through time and its implications for (i) the mantle carbon reservoir, (ii) its oxygen fugacity, (iii) the fluid / melt growth environment of diamonds, (iv) fractionation trends recorded in individual diamonds, and (v) diamond population studies using bulk combustion carbon isotope analysis.
deposit - Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya, Venetia, Wawa, Diavik
Abstract: Earth’s mantle is by far the largest silicate-hosted reservoir of carbon. Diamonds are unrivalled in their ability to record the cycle of mantle carbon and other volatiles over a vast portion of the Earth’s history. They are the product of ascending, cooling, carbon-saturated, metasomatic fluidsmelts and/or redox reactions, predominantly within peridotitic and eclogitic domains in the mantle lithosphere. This paper reports the results of a major secondary ion mass spectrometry (SIMS) carbon isotope study, carried out on 127 diamond samples, spanning a large range of geological time. Detailed transects across the incremental growth zones within each diamond were measured for C isotopes, N abundances and, for samples with N >~200 at.ppm, N isotopes. Given that all of the samples are fragments, recovered when the original crystals were broken to liberate their inclusions, 81 of the analytical traverses have confirmed growth direction context. 98 samples are from studies that have confirmed the dates of the individual diamonds through analysis of their silicate or sulphide inclusions, from source localities including Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya & Venetia. Additional samples come from Wawa (a minimum age) and Diavik where the samples are tied via inclusion paragenesis to published ages. The peridotitic dataset covers the age range of ~3.3 - 2.0 Ga, with the eclogitic data from 2.9 - 1.0 Ga. In total, 751 carbon isotope and nitrogen concentration measurements have been obtained (425 on peridotitic diamonds, and 326 on eclogitic diamonds) with 470 nitrogen isotope measurements (190 P, 280 E). We attempt to constrain the diamond carbon isotope record through time and its implications for (i) the mantle carbon reservoir, (ii) its oxygen fugacity, (iii) the fluid / melt growth environment of diamonds, (iv) fractionation trends recorded in individual diamonds, and (v) diamond population studies using bulk combustion carbon isotope analysis.
deposit - Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya, Venetia, Wawa, Diavik
Abstract: Earth’s mantle is by far the largest silicate-hosted reservoir of carbon. Diamonds are unrivalled in their ability to record the cycle of mantle carbon and other volatiles over a vast portion of the Earth’s history. They are the product of ascending, cooling, carbon-saturated, metasomatic fluidsmelts and/or redox reactions, predominantly within peridotitic and eclogitic domains in the mantle lithosphere. This paper reports the results of a major secondary ion mass spectrometry (SIMS) carbon isotope study, carried out on 127 diamond samples, spanning a large range of geological time. Detailed transects across the incremental growth zones within each diamond were measured for C isotopes, N abundances and, for samples with N >~200 at.ppm, N isotopes. Given that all of the samples are fragments, recovered when the original crystals were broken to liberate their inclusions, 81 of the analytical traverses have confirmed growth direction context. 98 samples are from studies that have confirmed the dates of the individual diamonds through analysis of their silicate or sulphide inclusions, from source localities including Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya & Venetia. Additional samples come from Wawa (a minimum age) and Diavik where the samples are tied via inclusion paragenesis to published ages. The peridotitic dataset covers the age range of ~3.3 - 2.0 Ga, with the eclogitic data from 2.9 - 1.0 Ga. In total, 751 carbon isotope and nitrogen concentration measurements have been obtained (425 on peridotitic diamonds, and 326 on eclogitic diamonds) with 470 nitrogen isotope measurements (190 P, 280 E). We attempt to constrain the diamond carbon isotope record through time and its implications for (i) the mantle carbon reservoir, (ii) its oxygen fugacity, (iii) the fluid / melt growth environment of diamonds, (iv) fractionation trends recorded in individual diamonds, and (v) diamond population studies using bulk combustion carbon isotope analysis.
deposit - Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya, Venetia, Wawa, Diavik
Abstract: Earth’s mantle is by far the largest silicate-hosted reservoir of carbon. Diamonds are unrivalled in their ability to record the cycle of mantle carbon and other volatiles over a vast portion of the Earth’s history. They are the product of ascending, cooling, carbon-saturated, metasomatic fluidsmelts and/or redox reactions, predominantly within peridotitic and eclogitic domains in the mantle lithosphere. This paper reports the results of a major secondary ion mass spectrometry (SIMS) carbon isotope study, carried out on 127 diamond samples, spanning a large range of geological time. Detailed transects across the incremental growth zones within each diamond were measured for C isotopes, N abundances and, for samples with N >~200 at.ppm, N isotopes. Given that all of the samples are fragments, recovered when the original crystals were broken to liberate their inclusions, 81 of the analytical traverses have confirmed growth direction context. 98 samples are from studies that have confirmed the dates of the individual diamonds through analysis of their silicate or sulphide inclusions, from source localities including Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya & Venetia. Additional samples come from Wawa (a minimum age) and Diavik where the samples are tied via inclusion paragenesis to published ages. The peridotitic dataset covers the age range of ~3.3 - 2.0 Ga, with the eclogitic data from 2.9 - 1.0 Ga. In total, 751 carbon isotope and nitrogen concentration measurements have been obtained (425 on peridotitic diamonds, and 326 on eclogitic diamonds) with 470 nitrogen isotope measurements (190 P, 280 E). We attempt to constrain the diamond carbon isotope record through time and its implications for (i) the mantle carbon reservoir, (ii) its oxygen fugacity, (iii) the fluid / melt growth environment of diamonds, (iv) fractionation trends recorded in individual diamonds, and (v) diamond population studies using bulk combustion carbon isotope analysis.
deposit - Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya, Venetia, Wawa, Diavik
Abstract: Earth’s mantle is by far the largest silicate-hosted reservoir of carbon. Diamonds are unrivalled in their ability to record the cycle of mantle carbon and other volatiles over a vast portion of the Earth’s history. They are the product of ascending, cooling, carbon-saturated, metasomatic fluidsmelts and/or redox reactions, predominantly within peridotitic and eclogitic domains in the mantle lithosphere. This paper reports the results of a major secondary ion mass spectrometry (SIMS) carbon isotope study, carried out on 127 diamond samples, spanning a large range of geological time. Detailed transects across the incremental growth zones within each diamond were measured for C isotopes, N abundances and, for samples with N >~200 at.ppm, N isotopes. Given that all of the samples are fragments, recovered when the original crystals were broken to liberate their inclusions, 81 of the analytical traverses have confirmed growth direction context. 98 samples are from studies that have confirmed the dates of the individual diamonds through analysis of their silicate or sulphide inclusions, from source localities including Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya & Venetia. Additional samples come from Wawa (a minimum age) and Diavik where the samples are tied via inclusion paragenesis to published ages. The peridotitic dataset covers the age range of ~3.3 - 2.0 Ga, with the eclogitic data from 2.9 - 1.0 Ga. In total, 751 carbon isotope and nitrogen concentration measurements have been obtained (425 on peridotitic diamonds, and 326 on eclogitic diamonds) with 470 nitrogen isotope measurements (190 P, 280 E). We attempt to constrain the diamond carbon isotope record through time and its implications for (i) the mantle carbon reservoir, (ii) its oxygen fugacity, (iii) the fluid / melt growth environment of diamonds, (iv) fractionation trends recorded in individual diamonds, and (v) diamond population studies using bulk combustion carbon isotope analysis.
deposit - Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya, Venetia, Wawa, Diavik
Abstract: Earth’s mantle is by far the largest silicate-hosted reservoir of carbon. Diamonds are unrivalled in their ability to record the cycle of mantle carbon and other volatiles over a vast portion of the Earth’s history. They are the product of ascending, cooling, carbon-saturated, metasomatic fluidsmelts and/or redox reactions, predominantly within peridotitic and eclogitic domains in the mantle lithosphere. This paper reports the results of a major secondary ion mass spectrometry (SIMS) carbon isotope study, carried out on 127 diamond samples, spanning a large range of geological time. Detailed transects across the incremental growth zones within each diamond were measured for C isotopes, N abundances and, for samples with N >~200 at.ppm, N isotopes. Given that all of the samples are fragments, recovered when the original crystals were broken to liberate their inclusions, 81 of the analytical traverses have confirmed growth direction context. 98 samples are from studies that have confirmed the dates of the individual diamonds through analysis of their silicate or sulphide inclusions, from source localities including Argyle, De Beers Pool, Jwaneng, Orapa, Udachnaya & Venetia. Additional samples come from Wawa (a minimum age) and Diavik where the samples are tied via inclusion paragenesis to published ages. The peridotitic dataset covers the age range of ~3.3 - 2.0 Ga, with the eclogitic data from 2.9 - 1.0 Ga. In total, 751 carbon isotope and nitrogen concentration measurements have been obtained (425 on peridotitic diamonds, and 326 on eclogitic diamonds) with 470 nitrogen isotope measurements (190 P, 280 E). We attempt to constrain the diamond carbon isotope record through time and its implications for (i) the mantle carbon reservoir, (ii) its oxygen fugacity, (iii) the fluid / melt growth environment of diamonds, (iv) fractionation trends recorded in individual diamonds, and (v) diamond population studies using bulk combustion carbon isotope analysis.
Abstract: Melt/fluid inclusions in diamonds provide important evidence for mantle diamond-forming fluids or melts. By now, the major characteristics of the composition of microinclusions have been analyzed in diamonds from several kimberlite provinces and pipes worldwide [1-4]. Here we report the first data on the composition of parent diamondforming melts for diamonds from the Arkhangelsk kimberlite province. After the study of morphology, specialty of the internal structure, and distribution of microinclusions in diamonds, 10 single crystals were selected from the 31 diamonds of the representative collection. The studied crystals may be divided into two groups: cuboids and coated diamonds. The crystals have grayish yellow or dark gray colors and are almost nontransparent due to the high content of microinclusions. Polished slices of these diamonds were studied by IR-spectroscopy, which allowed us to calculate the content of nitrogen defects, as well as the content of water and carbonates in microinclusions. X-ray spectral analyses allowed to study the composition of fluid/melt microinclusions and showed that they were essentially carbonate-silicate with significant variations between these two end-members. All inclusions contain water, with the highest H2O/CO2 in highly siliceous inclusions. Unlike diamonds from Canada and South Africa [1, 2], the studied inclusions in diamionds from the Arkhangelsk province are almost free of chlorides. Comparison of the data obtained with the database on fliud/melt inclusions in diamonds worldwide shows similar of Arkhangelsk diamonds to some diamonds from Yakutia [3, 4], and the data obtained are the most similar to the composition of microinclusions in diamonds from the Internatsionalnaya pipe (Yakutia).
Abstract: Polycrystalline diamond aggregates (framesites, boart, diamondite) are an understudied variety of mantle diamond, but can make up 20% of the production in some Group I kimberlites. Their polycrystalline nature indicates rapid precipitation from carbon-oversaturated fluids and individual PDAs often contain a chemically heterogeneous suite of websteritic and pyroxenitic inclusions and minerals intimately intergrown with the diamond crystals. Geochemical and microstructural evidence suggests that fluid-driven redox reactions with lithospheric material occurring episodically over millions of years play a major role in freezing carbon in the subcratonic lithosphere (Jacob et al., 2000; 2016; Mikhail et al., 2014). A suite of 39 samples from the Venetia kimberlite pipe in South Africa allows a more detailed look at the diamondforming fluids. 13C values in the diamonds measured by secondary ion mass spectrometry range from +2 to -28 and cover the entire range for PDA from the literature. Nitrogen concentrations are mostly very low (less than 100 at ppm), but reach up to 2660 at ppm in individual samples. These high nitrogen concentrations in concert with mostly positive 15N values of up to +17 and some very negative 3C values suggest crustal material as the source of the nitrogen and the carbon. However, detailed analysis of the sample provides evidence for a more complex growth history followed by alteration. Individual diamond crystals show complex growth zonations by cathodoluminescence imaging that can be related with the carbon and nitrogen isotopic compositions and points to growth incorporating several pulses of carbon-nitrogen fluid with distinct isotopic compositions. Most of these growth events show decoupled carbon and nitrogen systematics. In addition, EBSD identifies deformation and recrystallization and nitrogen aggregation states range from pure IaA to pure IaB, supporting a heterogeneous and episodic growth history.
Africa, Zimbabwe. Australia, Canada, Northwest Territories, South Africa, Botswana
deposit - Murowa, Argyle, Diavik, Venetia, Orapa
Abstract: FTIR maps of diamond plates, cut through the centre of growth, contain abundant information about changing defect concentrations from core to rim. These data can, in principle, be interpreted in terms of the variation in conditions of diamond growth and the temperatures experienced by the diamond during the period of mantle residence between growth and exhumation. Many diamonds show multiple growth zones that can be observed by cathodoluminescence. Importantly, the combination of nitrogen concentration and nitrogen aggregation measured by FTIR can be used to determine whether the growth zones are of similar or very different ages (Kohn et al., 2016). In this study, we use automated fitting of several thousand individual spectra within each FTIR map to define a model temperature for each pixel using the Python program, QUIDDIT. We then use a two-stage aggregation model to constrain potential temperature-time histories for each diamond. To take full advantage of the temperature history recorded by zoned diamonds, radiometric ages of inclusions are required. If the growth ages of each zone and the date of exhumation are well-known, then a model temperature can be calculated for each zone. The combination of zone-specific ages and improved quality and processing of FTIR spectra is able to provide unique new insights into the thermal history of diamondbearing lithospheric mantle. For the first time we will be able to use the N defects in diamonds to work out whether a particular location in the lithosphere has heated or cooled over long periods of geological time. The implications for the mechanism of formation of lithosphere will be discussed. We will illustrate the approach using examples of zoned diamonds from Murowa (Zimbabwe), Argyle (Australia), Diavik (Canada), Venetia (South Africa) and Orapa (Botswana).
Africa, Zimbabwe. Australia, Canada, Northwest Territories, South Africa, Botswana
deposit - Murowa, Argyle, Diavik, Venetia, Orapa
Abstract: FTIR maps of diamond plates, cut through the centre of growth, contain abundant information about changing defect concentrations from core to rim. These data can, in principle, be interpreted in terms of the variation in conditions of diamond growth and the temperatures experienced by the diamond during the period of mantle residence between growth and exhumation. Many diamonds show multiple growth zones that can be observed by cathodoluminescence. Importantly, the combination of nitrogen concentration and nitrogen aggregation measured by FTIR can be used to determine whether the growth zones are of similar or very different ages (Kohn et al., 2016). In this study, we use automated fitting of several thousand individual spectra within each FTIR map to define a model temperature for each pixel using the Python program, QUIDDIT. We then use a two-stage aggregation model to constrain potential temperature-time histories for each diamond. To take full advantage of the temperature history recorded by zoned diamonds, radiometric ages of inclusions are required. If the growth ages of each zone and the date of exhumation are well-known, then a model temperature can be calculated for each zone. The combination of zone-specific ages and improved quality and processing of FTIR spectra is able to provide unique new insights into the thermal history of diamondbearing lithospheric mantle. For the first time we will be able to use the N defects in diamonds to work out whether a particular location in the lithosphere has heated or cooled over long periods of geological time. The implications for the mechanism of formation of lithosphere will be discussed. We will illustrate the approach using examples of zoned diamonds from Murowa (Zimbabwe), Argyle (Australia), Diavik (Canada), Venetia (South Africa) and Orapa (Botswana).
Africa, Zimbabwe. Australia, Canada, Northwest Territories, South Africa, Botswana
deposit - Murowa, Argyle, Diavik, Venetia, Orapa
Abstract: FTIR maps of diamond plates, cut through the centre of growth, contain abundant information about changing defect concentrations from core to rim. These data can, in principle, be interpreted in terms of the variation in conditions of diamond growth and the temperatures experienced by the diamond during the period of mantle residence between growth and exhumation. Many diamonds show multiple growth zones that can be observed by cathodoluminescence. Importantly, the combination of nitrogen concentration and nitrogen aggregation measured by FTIR can be used to determine whether the growth zones are of similar or very different ages (Kohn et al., 2016). In this study, we use automated fitting of several thousand individual spectra within each FTIR map to define a model temperature for each pixel using the Python program, QUIDDIT. We then use a two-stage aggregation model to constrain potential temperature-time histories for each diamond. To take full advantage of the temperature history recorded by zoned diamonds, radiometric ages of inclusions are required. If the growth ages of each zone and the date of exhumation are well-known, then a model temperature can be calculated for each zone. The combination of zone-specific ages and improved quality and processing of FTIR spectra is able to provide unique new insights into the thermal history of diamondbearing lithospheric mantle. For the first time we will be able to use the N defects in diamonds to work out whether a particular location in the lithosphere has heated or cooled over long periods of geological time. The implications for the mechanism of formation of lithosphere will be discussed. We will illustrate the approach using examples of zoned diamonds from Murowa (Zimbabwe), Argyle (Australia), Diavik (Canada), Venetia (South Africa) and Orapa (Botswana).
Africa, Zimbabwe. Australia, Canada, Northwest Territories, South Africa, Botswana
deposit - Murowa, Argyle, Diavik, Venetia, Orapa
Abstract: FTIR maps of diamond plates, cut through the centre of growth, contain abundant information about changing defect concentrations from core to rim. These data can, in principle, be interpreted in terms of the variation in conditions of diamond growth and the temperatures experienced by the diamond during the period of mantle residence between growth and exhumation. Many diamonds show multiple growth zones that can be observed by cathodoluminescence. Importantly, the combination of nitrogen concentration and nitrogen aggregation measured by FTIR can be used to determine whether the growth zones are of similar or very different ages (Kohn et al., 2016). In this study, we use automated fitting of several thousand individual spectra within each FTIR map to define a model temperature for each pixel using the Python program, QUIDDIT. We then use a two-stage aggregation model to constrain potential temperature-time histories for each diamond. To take full advantage of the temperature history recorded by zoned diamonds, radiometric ages of inclusions are required. If the growth ages of each zone and the date of exhumation are well-known, then a model temperature can be calculated for each zone. The combination of zone-specific ages and improved quality and processing of FTIR spectra is able to provide unique new insights into the thermal history of diamondbearing lithospheric mantle. For the first time we will be able to use the N defects in diamonds to work out whether a particular location in the lithosphere has heated or cooled over long periods of geological time. The implications for the mechanism of formation of lithosphere will be discussed. We will illustrate the approach using examples of zoned diamonds from Murowa (Zimbabwe), Argyle (Australia), Diavik (Canada), Venetia (South Africa) and Orapa (Botswana).
Africa, Zimbabwe. Australia, Canada, Northwest Territories, South Africa, Botswana
deposit - Murowa, Argyle, Diavik, Venetia, Orapa
Abstract: FTIR maps of diamond plates, cut through the centre of growth, contain abundant information about changing defect concentrations from core to rim. These data can, in principle, be interpreted in terms of the variation in conditions of diamond growth and the temperatures experienced by the diamond during the period of mantle residence between growth and exhumation. Many diamonds show multiple growth zones that can be observed by cathodoluminescence. Importantly, the combination of nitrogen concentration and nitrogen aggregation measured by FTIR can be used to determine whether the growth zones are of similar or very different ages (Kohn et al., 2016). In this study, we use automated fitting of several thousand individual spectra within each FTIR map to define a model temperature for each pixel using the Python program, QUIDDIT. We then use a two-stage aggregation model to constrain potential temperature-time histories for each diamond. To take full advantage of the temperature history recorded by zoned diamonds, radiometric ages of inclusions are required. If the growth ages of each zone and the date of exhumation are well-known, then a model temperature can be calculated for each zone. The combination of zone-specific ages and improved quality and processing of FTIR spectra is able to provide unique new insights into the thermal history of diamondbearing lithospheric mantle. For the first time we will be able to use the N defects in diamonds to work out whether a particular location in the lithosphere has heated or cooled over long periods of geological time. The implications for the mechanism of formation of lithosphere will be discussed. We will illustrate the approach using examples of zoned diamonds from Murowa (Zimbabwe), Argyle (Australia), Diavik (Canada), Venetia (South Africa) and Orapa (Botswana).
Neues Jahrbuch fur Mineralogie, Vol. 195, pp. 145-153.
Australia
deposit - Argyle
Abstract: Contact twinning with the so-called "macle" form or other shapes are often found in natural diamond crystals. However, the surface microtopographic features associated with twinning have been less investigated. Here, the surface dissolution and growth features seen on the twin boundaries, including the re-entrant angles revealed by differential interference contrast microscope and SEM techniques in 170 natural diamond crystals mainly from Argle mine, Australia are described and summarized. The hexagonal pits, rhombic pits along with higher symmetry observed at the twin boundaries together with dislocations and their formation processes are discussed.
Abstract: The Wajrakarur kimberlite field (WKF) records >45 pipes so far, majority being diamodiferous. In addition to pipe-10 (Anumpalli) and 11 (Dibbasanipalli) discovered by the Geological Survey of India, of late, Rio Tinto Group has discovered three more outcropping pipes in this area (east of Dibbasanipalli, west of Anumpalli and Khaderpet) and termed all these five pipes as Anumpalli kimberltie cluster (AKC). The AKC pipes contain crustal granitoid xenoliths. The Khaderpet and Dibbasanipalli east pipes show effects of fenitisation in the country rock granitoids and are intensely chloritised kimberlite granite breccias; however, the former is unique in having its association with carbonatite (sovite) intrusion. Petrographically, the AKC kimberlites exhibit inequigranular texture resulted by anhedral to subhedral olivine macrocrysts and pseudomorphs, phenocrysts of Crdiopside, ilmenite, perovskite and minor or no amounts of phologopite with two generations of olivine within a finegrained matrix of same mineral phases. Based on the major element geochemistry the AKC pipes are classified as Group- I archetypal. Based on trace element modeling, the AKC pipes appear to be originated form garnet lherzolite source with residual garnet of 0.5 to 5%, associated with stable continental and/or orogenic area and remarkably belong to non-subduction environment. The observed LREE enrichment and low HREE cencentrations in the AKC, is consistent with inferior degrees of partial melting (0.1 to 2%). The AKC pipes appear to have originated from a hydrous magma enriched in volatiles. Exploration evidences support that kimberlites of the AKC are diamodiferous. The calculated diamond grade (DG) values of the AKC pipes are high (3.43 to 8.48) which are inversely proportional to the TiO2 content. In the binary diagram of Ta and Sc (ppm), the AKC pipes plot in the field of ‘Fe-Ti diamondiferous kimberlites’. In the Fe2O3 (wt %) vs. Y (ppm) diagram, the AKC pipes plot in the ‘prospective’ field. The diamondiferous nature of the AKC pipes indicates the conditions of diamond preservation at metastable phases in crustal environment during rapid ascent of kimberlite melt to the surface from the deep mantle, which is supported by low density and ultralow viscosity of these intrusions.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0625-4 13p.
Australia, Western Australia
deposit - Argyle
Abstract: Underground mining and deep drilling of the richly diamondiferous ~1.2 Ga Argyle lamproite in Western Australia has prompted a re-evaluation of the geology of the pipe. Argyle is considered to be a composite pipe that formed by the coalescence of several diatremes and has been offset and elongated by post-emplacement faulting. Recent geological studies have recognised at least five distinct volcaniclastic lamproite lithofacies with differing diamond grades. The new data suggest that the centre of the southern (main) diatreme is occupied by well-bedded, olivine lamproite lapilli tuff with very high diamond grades (>10 ct/t). Characteristic features include a clast-supported fabric and high modal abundance of densely packed lamproite lapilli and coarse-grained, likely mantle-derived olivine now replaced by serpentine and/or talc. The persistence of small-scale graded and cross-bedding in this lithofacies to depths of ~1.5 km below the original surface prior to erosion suggests phreatomagmatic volcanism forming the diatreme was syn-eruptively accompanied by subsidence of the tephra, maintaining a steep-walled diatreme in the water-saturated country rock sediments.
Africa, South Africa, Guinea, South America, Brazil
deposit - Kankan, Jagersfontein, Juina
Abstract: Inclusions in super-deep diamonds provide a unique window to the sublithospheric mantle (e.g. [1-4]). Here we present oxygen isotopes for Kankan majoritic garnet and former bridgmanite inclusions. The clustering of Kankan majorites around a ?18O of +9‰ is nearly identical to those reported from Jagersfontein [1]. This elevated and nearly constant ?18O signal indicates homogenization of partial melts from the uppermost part of altered basaltic slabs. Conversely, ?18O values in Juina majorites are highly variable [2] due to crystallization from small, discrete melt pockets in a heterogeneous eclogitic source. While all these majorites have eclogitic/pyroxenitic Cr2O3 and CaO contents, charge-balance for Si[VI] is achieved very differently, with Jagersfontein [3], Kankan [4], and Juina [2] majorites transitioning from eclogitic Na[VIII]Si[VI] to peridotitic-pyroxenitic [5] Mg[VI]Si[VI] substitutions. We interpret this shift as the result of homogenized eclogitic partial melts infiltrating and reacting with adjacent pyrolitic mantle at Kankan and Jagersfontein. Increases in Mg# and Cr2O3 with reductions in ?18O support this reaction. This model is in agreement with recent experiments in which majorites and diamonds form from a reaction of slab-derived carbonatite with reduced pyrolite at 300-700 km depth [6]. The Kankan diamonds also provide an opportunity to establish the chemical environment of the lower mantle. Four inclusions of MgSiO3, inferred to be former bridgmanite [4], provide the first-measured ?18O values for lower mantle samples. These values suggest derivation from primitive mantle, or unaltered subducted oceanic lithospheric mantle. The Kankan super-deep inclusions thus provide a cross-section of deep mantle that highlights slab-pyrolite reactions in the asthenosphere and primitive compositions in the lower mantle.
Africa, South Africa, Guinea, South America, Brazil
deposit - Kankan, Jagersfontein, Juina
Abstract: Inclusions in super-deep diamonds provide a unique window to the sublithospheric mantle (e.g. [1-4]). Here we present oxygen isotopes for Kankan majoritic garnet and former bridgmanite inclusions. The clustering of Kankan majorites around a ?18O of +9‰ is nearly identical to those reported from Jagersfontein [1]. This elevated and nearly constant ?18O signal indicates homogenization of partial melts from the uppermost part of altered basaltic slabs. Conversely, ?18O values in Juina majorites are highly variable [2] due to crystallization from small, discrete melt pockets in a heterogeneous eclogitic source. While all these majorites have eclogitic/pyroxenitic Cr2O3 and CaO contents, charge-balance for Si[VI] is achieved very differently, with Jagersfontein [3], Kankan [4], and Juina [2] majorites transitioning from eclogitic Na[VIII]Si[VI] to peridotitic-pyroxenitic [5] Mg[VI]Si[VI] substitutions. We interpret this shift as the result of homogenized eclogitic partial melts infiltrating and reacting with adjacent pyrolitic mantle at Kankan and Jagersfontein. Increases in Mg# and Cr2O3 with reductions in ?18O support this reaction. This model is in agreement with recent experiments in which majorites and diamonds form from a reaction of slab-derived carbonatite with reduced pyrolite at 300-700 km depth [6]. The Kankan diamonds also provide an opportunity to establish the chemical environment of the lower mantle. Four inclusions of MgSiO3, inferred to be former bridgmanite [4], provide the first-measured ?18O values for lower mantle samples. These values suggest derivation from primitive mantle, or unaltered subducted oceanic lithospheric mantle. The Kankan super-deep inclusions thus provide a cross-section of deep mantle that highlights slab-pyrolite reactions in the asthenosphere and primitive compositions in the lower mantle.
Africa, South Africa, Guinea, South America, Brazil
deposit - Kankan, Jagersfontein, Juina
Abstract: Inclusions in super-deep diamonds provide a unique window to the sublithospheric mantle (e.g. [1-4]). Here we present oxygen isotopes for Kankan majoritic garnet and former bridgmanite inclusions. The clustering of Kankan majorites around a ?18O of +9‰ is nearly identical to those reported from Jagersfontein [1]. This elevated and nearly constant ?18O signal indicates homogenization of partial melts from the uppermost part of altered basaltic slabs. Conversely, ?18O values in Juina majorites are highly variable [2] due to crystallization from small, discrete melt pockets in a heterogeneous eclogitic source. While all these majorites have eclogitic/pyroxenitic Cr2O3 and CaO contents, charge-balance for Si[VI] is achieved very differently, with Jagersfontein [3], Kankan [4], and Juina [2] majorites transitioning from eclogitic Na[VIII]Si[VI] to peridotitic-pyroxenitic [5] Mg[VI]Si[VI] substitutions. We interpret this shift as the result of homogenized eclogitic partial melts infiltrating and reacting with adjacent pyrolitic mantle at Kankan and Jagersfontein. Increases in Mg# and Cr2O3 with reductions in ?18O support this reaction. This model is in agreement with recent experiments in which majorites and diamonds form from a reaction of slab-derived carbonatite with reduced pyrolite at 300-700 km depth [6]. The Kankan diamonds also provide an opportunity to establish the chemical environment of the lower mantle. Four inclusions of MgSiO3, inferred to be former bridgmanite [4], provide the first-measured ?18O values for lower mantle samples. These values suggest derivation from primitive mantle, or unaltered subducted oceanic lithospheric mantle. The Kankan super-deep inclusions thus provide a cross-section of deep mantle that highlights slab-pyrolite reactions in the asthenosphere and primitive compositions in the lower mantle.
Abstract: Yogo Gulch in central Montana is one of the most important gem deposits in the United States. Although very little material has been recovered there in recent years, it has produced several million carats of rough sapphire over the course of its history (Voynick, 2001). These stones, known for their vibrant untreated blue color and high clarity, have always commanded a price premium, especially in sizes larger than 0.75 ct. This paper offers a thorough gemological characterization of Yogo sapphire, which may be unfamiliar to many gemologists. Fortunately, Yogo sapphires are unique and experienced gemologists can easily separate them from gem corundum of different geographic origins throughout the world, making it possible to determine the provenance of important stones from this deposit.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0632-5 20p.
Canada, Nunavut, Melville Peninsula
deposit - Pelly Bay, Darby, Aviat, Qilalugaq
Abstract: Detailed geochronology along with petrographic, mineralogical and geochemical studies have been conducted on recently found diamond-bearing kimberlitic and related rocks in the Rae Craton at Aviat and Qilalugaq, Melville Peninsula, north-east Canada. Magmatic rocks from the Aviat pipes have geochemical (both bulk rock and isotopic) and mineralogical signatures (e.g., core to rim Al and Ba enrichment in phlogopite) similar to Group I kimberlite. In contrast, Aviat intrusive sheets are similar to ‘micaceous’ Group II kimberlite (orangeite) in their geochemical and mineralogical characteristics (e.g., phlogopite and spinel compositions, highly enriched Sr isotopic signature). Qilalugaq rocks with the least crustal contamination have geochemical and mineralogical signatures [e.g., high SiO2, Al2O3 and H2O; low TiO2 and CO2; less fractionated REE (rare earth elements), presence of primary clinopyroxene, phlogopite and spinel compositions] that are similar to features displayed by olivine lamproites from Argyle, Ellendale and West Greenland. The Naujaat dykes, in the vicinity of Qilalugaq, are highly altered due to extensive silicification and carbonation. However, their bulk rock geochemical signature and phlogopite chemistry are similar to Group I kimberlite. U-Pb perovskite geochronology reveals that Aviat pipes and all rocks from Qilalugaq have an early Cambrian emplacement age (540-530 Ma), with the Aviat sheets being ~30 Ma younger. This volatile-rich potassic ultramafic magmatism probably formed by varying degrees of involvement of asthenospheric and lithospherically derived melts. The spectrum of ages and compositions are similar to equivalent magmatic rocks observed from the nearby north-eastern North America and Western Greenland. The ultimate trigger for this magmatism could be linked to Neoproterozoic continental rifting during the opening of the Iapetus Ocean and breakup of the Rodinia supercontinent.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0632-5 20p.
Canada, Nunavut, Melville Peninsula
deposit - Pelly Bay, Darby, Aviat, Qilalugaq
Abstract: Detailed geochronology along with petrographic, mineralogical and geochemical studies have been conducted on recently found diamond-bearing kimberlitic and related rocks in the Rae Craton at Aviat and Qilalugaq, Melville Peninsula, north-east Canada. Magmatic rocks from the Aviat pipes have geochemical (both bulk rock and isotopic) and mineralogical signatures (e.g., core to rim Al and Ba enrichment in phlogopite) similar to Group I kimberlite. In contrast, Aviat intrusive sheets are similar to ‘micaceous’ Group II kimberlite (orangeite) in their geochemical and mineralogical characteristics (e.g., phlogopite and spinel compositions, highly enriched Sr isotopic signature). Qilalugaq rocks with the least crustal contamination have geochemical and mineralogical signatures [e.g., high SiO2, Al2O3 and H2O; low TiO2 and CO2; less fractionated REE (rare earth elements), presence of primary clinopyroxene, phlogopite and spinel compositions] that are similar to features displayed by olivine lamproites from Argyle, Ellendale and West Greenland. The Naujaat dykes, in the vicinity of Qilalugaq, are highly altered due to extensive silicification and carbonation. However, their bulk rock geochemical signature and phlogopite chemistry are similar to Group I kimberlite. U-Pb perovskite geochronology reveals that Aviat pipes and all rocks from Qilalugaq have an early Cambrian emplacement age (540-530 Ma), with the Aviat sheets being ~30 Ma younger. This volatile-rich potassic ultramafic magmatism probably formed by varying degrees of involvement of asthenospheric and lithospherically derived melts. The spectrum of ages and compositions are similar to equivalent magmatic rocks observed from the nearby north-eastern North America and Western Greenland. The ultimate trigger for this magmatism could be linked to Neoproterozoic continental rifting during the opening of the Iapetus Ocean and breakup of the Rodinia supercontinent.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0632-5 20p.
Canada, Nunavut, Melville Peninsula
deposit - Pelly Bay, Darby, Aviat, Qilalugaq
Abstract: Detailed geochronology along with petrographic, mineralogical and geochemical studies have been conducted on recently found diamond-bearing kimberlitic and related rocks in the Rae Craton at Aviat and Qilalugaq, Melville Peninsula, north-east Canada. Magmatic rocks from the Aviat pipes have geochemical (both bulk rock and isotopic) and mineralogical signatures (e.g., core to rim Al and Ba enrichment in phlogopite) similar to Group I kimberlite. In contrast, Aviat intrusive sheets are similar to ‘micaceous’ Group II kimberlite (orangeite) in their geochemical and mineralogical characteristics (e.g., phlogopite and spinel compositions, highly enriched Sr isotopic signature). Qilalugaq rocks with the least crustal contamination have geochemical and mineralogical signatures [e.g., high SiO2, Al2O3 and H2O; low TiO2 and CO2; less fractionated REE (rare earth elements), presence of primary clinopyroxene, phlogopite and spinel compositions] that are similar to features displayed by olivine lamproites from Argyle, Ellendale and West Greenland. The Naujaat dykes, in the vicinity of Qilalugaq, are highly altered due to extensive silicification and carbonation. However, their bulk rock geochemical signature and phlogopite chemistry are similar to Group I kimberlite. U-Pb perovskite geochronology reveals that Aviat pipes and all rocks from Qilalugaq have an early Cambrian emplacement age (540-530 Ma), with the Aviat sheets being ~30 Ma younger. This volatile-rich potassic ultramafic magmatism probably formed by varying degrees of involvement of asthenospheric and lithospherically derived melts. The spectrum of ages and compositions are similar to equivalent magmatic rocks observed from the nearby north-eastern North America and Western Greenland. The ultimate trigger for this magmatism could be linked to Neoproterozoic continental rifting during the opening of the Iapetus Ocean and breakup of the Rodinia supercontinent.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0632-5 20p.
Canada, Nunavut, Melville Peninsula
deposit - Pelly Bay, Darby, Aviat, Qilalugaq
Abstract: Detailed geochronology along with petrographic, mineralogical and geochemical studies have been conducted on recently found diamond-bearing kimberlitic and related rocks in the Rae Craton at Aviat and Qilalugaq, Melville Peninsula, north-east Canada. Magmatic rocks from the Aviat pipes have geochemical (both bulk rock and isotopic) and mineralogical signatures (e.g., core to rim Al and Ba enrichment in phlogopite) similar to Group I kimberlite. In contrast, Aviat intrusive sheets are similar to ‘micaceous’ Group II kimberlite (orangeite) in their geochemical and mineralogical characteristics (e.g., phlogopite and spinel compositions, highly enriched Sr isotopic signature). Qilalugaq rocks with the least crustal contamination have geochemical and mineralogical signatures [e.g., high SiO2, Al2O3 and H2O; low TiO2 and CO2; less fractionated REE (rare earth elements), presence of primary clinopyroxene, phlogopite and spinel compositions] that are similar to features displayed by olivine lamproites from Argyle, Ellendale and West Greenland. The Naujaat dykes, in the vicinity of Qilalugaq, are highly altered due to extensive silicification and carbonation. However, their bulk rock geochemical signature and phlogopite chemistry are similar to Group I kimberlite. U-Pb perovskite geochronology reveals that Aviat pipes and all rocks from Qilalugaq have an early Cambrian emplacement age (540-530 Ma), with the Aviat sheets being ~30 Ma younger. This volatile-rich potassic ultramafic magmatism probably formed by varying degrees of involvement of asthenospheric and lithospherically derived melts. The spectrum of ages and compositions are similar to equivalent magmatic rocks observed from the nearby north-eastern North America and Western Greenland. The ultimate trigger for this magmatism could be linked to Neoproterozoic continental rifting during the opening of the Iapetus Ocean and breakup of the Rodinia supercontinent.
Abstract: Diamond xenocrysts and eclogite-hosted diamonds from the Lahtojoki kimberlite (Karelian craton, Finland) indicate metasomatism of the deep lithosphere by N-rich, relatively reduced fluids. P-T-fO2 constraints show that all eclogites were derived from near the base of the lithospheric mantle (>5 GPa), but only the diamond-bearing samples are relatively reduced (?FMQ-3.5 vs. -1.7 for barren eclogites). The Lahtojoki diamonds show evidence of formation from reduced mantle-derived carbon, based on the restricted range of ?13C values (-3 and -7.8 ‰; n = 67) that form a negativelyskewed distribution. This reduced CHO fluid was also anomalously N-rich, based on the diamond N contents that range up to 1830 at. ppm. While N-rich sources for eclogiteassociated diamonds are often linked to recycled crustal materials, in this case we prefer derivation from K-rich cratonic mantle metasomes due to lack of firm crustal geochemical signatures in the eclogites (?18O = 5.7 - 5.9 ‰), in addition to the magmatic history of the Karelian craton. The Karelian craton has been periodically intruded by Krich alkaline lamprophyres, Group-2 kimberlites and olivine lamproites from 1800 to 700 Ma. Such K-rich ultramafic alkaline magmatism is likely linked to phlogopite-rich metasomes, which may represent significant repositories of N (NH4+ substitution for K+). Because the Lahtojoki eclogites resided near the base of the lithospheric mantle, they would have been susceptible to interaction with ascending asthenosphere-derived C-bearing fluids/melts, which were reducing. Following ingress into and interaction with the Krich metasomatised Karelian mantle lithosphere, the increasingly N-enriched, CH4-bearing fluids precipitated diamond during interaction with relatively oxidized eclogite wall rock. In contrast to the prevalent oxidizing effects of mantle metasomatism as identified within cratonic lithosphere-derived samples from worldwide locations, the eclogite-hosted diamonds at Lahtojoki represent a natural example of metasomatic overprinting that was highly reducing.
Abstract: This study investigates the color origin of 40 natural Fancy Dark brown-black round brilliant diamonds from the Marange alluvial deposits in eastern Zimbabwe. Visual observations show that the dark appearance of the Marange diamonds is due to a combination of graphite micro-inclusions (associated with methane), graphite needles, and dark brown radiation stains that occur along internal fractures. The GR1 (V0) defect, typically formed during natural and artificial irradiation, is observed in the optical spectra of 43% of the diamonds, al- though its intensity is too low to significantly impact the bodycolor. Natural irradiation in these diamonds is likely related to their billion-year residence in the Umkondo conglomerate, which is known to contain radioac- tive minerals such as zircon. Aside from radiation staining, irradiation-damaged diamond appears non-lumines- cent in DiamondView images and shows a weaker, broader diamond peak (at 1332 cm?1) in Raman spectroscopy. Brown coloration of the radiation stains is due to heating of the diamonds during later regional metamorphism, which also facilitated the formation of the H3 (NVN0) and NiN complexes.
Abstract: The first studies of diamonds in eclogitic xenoliths from the Komsomolskaya kimberlite pipe are described. Among round and oval-shaped xenoliths with diamond ingrowths, samples with a garnet content of 40-90% of the xenolith volume dominate. Two eclogite samples contain grains of accessory rutile; a kyanite sample is also revealed. Certain samples contain two or more crystals of diamonds. Diamonds with an octahedral habit and crystals with transitional habits, which belong to an octahedral-rhombic dodecahedral row, dominate in eclogites; there are many variety VIII aggregates. A high concentration of structural nitrogen, commonly in the A form, was registered in most of the crystals. Diamonds with a small content of nitrogen impurities, 40-67% in the B1 form, are present in a number of xenoliths. The calculated temperatures of the formation of eclogitic xenoliths is 1100-1300°C. Diversity in the impurity compositions of diamonds in the same xenolith shows that these diamonds were formed at various times and in different settings. The diamond position in xenoliths, the various level of nitrogen aggregation in the diamonds, and a number of other factors point to the later formation of the diamonds, as compared to minerals of eclogites, from fluid or fluid-melts in the process of metasomatosis.
Abstract: Diamonds containing fluid inclusions provide the most direct samples of upper mantle fluids. In eclogites, diamond can form by pH drop during fluid-rock interaction. However, in peridotites, the cause of the chemical evolution of the fluids and minerals, including the wide range of observed salinities involved, are still unclear. Here we used new experimental calibrations of the Deep Earth Water model involving organic and inorganic complexes of the major rockforming elements to show that fluid mixing can cause diamond formation in the peridotitic environment. Models of the saline and carbonatitic fluid inclusion compositions consistent with the chemistry of measured solid inclusions in Panda diamonds were used to simulate the irreversible, chemical mass transfer when a carbonatitic fluid infiltrates harzburgite containing a saline fluid at 950°C and 4.5 GPa. Simultaneous oxidation of aqueous hydrocarbons in the peridotitic fluid and reduction of the organic acid anion formate as well as bicarbonate in the carbonatitic fluid during mixing and reaction with harzburgite resulted in the formation of diamond, olivine, and garnet, and increases in the logfo2 and pH. Olivine was predicted to become more Ferich and garnet more Ca and Fe-rich with reaction progress, in agreement with reported temporal trends in the composition of mineral inclusions from octahedral cores to coated rims on Panda diamonds. Aqueous phase concentrations of all elements changed consistent with measured trends in fluid inclusion compositions from saline to less saline. For comparison, we also simulated a saline fluid infiltrating a harzburgite containing a carbonatitic fluid. Diamond again formed, but the compositional trends of the silicate minerals and the trend of salinity with reaction progress were all in the opposite direction to data from the Panda diamonds. Overall, our study strongly suggests that mixing of fluids containing carbon from both reduced and oxidized sources, and simultaneous reaction with harzburgite can cause precipitation of diamond, without the need for triggering by temperature or pressure changes, while adding Ca and Fe to the sub-lithospheric mantle.
Abstract: Volcanic pipes, or maar-diatreme volcanoes, form during explosive eruptions of mantle-derived magmas near Earth's surface. Impressive examples are the carrot-shaped, downward tapering structures formed by kimberlite magmas. Kimberlites originate from >150 km depth within Earth's mantle beneath thick continental roots, away from tectonic plate margins. Kimberlite pipes can be significant diamond deposits, and the complex architecture revealed during exploration and mining is ascribed to repeated magma injections leading to multiple eruptions. Repeated magmatic pulses cause diatremes to widen and grow downward, forming kilometer-sized subterranean structures. However, the time-resolved evolution of kimberlite pipe systems is largely unknown. We present the first U/Pb perovskite ages for newly discovered kimberlite dikes (1139.8 ± 4.8 Ma) that cut through the volcaniclastic infill of the Premier kimberlite pipe (1153.3 ± 5.3 Ma) at Cullinan Diamond Mine, South Africa. The ages reveal that renewed kimberlite volcanic activity occurred, at a minimum, 3 m.y. after the main pipe formation. This finding suggests that the largest kimberlite pipes, and maar-diatreme volcanoes in general, may be magmatically active for several millions of years, which conflicts with this volcanism being described as 'monogenetic' at millennia time scales. Exemplified by Tier-1 diamond deposits on the Kaapvaal craton, long-lasting kimberlite volcanic activity may be an important factor in growing large diatremes, plus enabling effective transport of mantle cargo from the diamond stability field to Earth's surface.
Abstract: Archean supracrustal rocks (i.e. chemical sediments and metavolcanics) preserve sulfur Mass Independent Fractionations (MIF) that originate from photochemical reactions occurring in atmosphere before the great oxygenation event, 2.45 Ga. Reduced and oxidized aerosols were produced by photochemistry and respectively carry 33S enrichment (?33S > 0‰) and depletion (?33S < 0‰). The relative abundance of the minor isotope of sulfur (36S) was also affected by MIF in such a way that compact negative correlation exists between ?33S and ?36S. For much of Archean sediments, ?36S /?33S? -1, while slight variation of this slope have been attributed to minor change in the chemical composition of the atmosphere affecting global MIF source mechanism. On another hand, 36S abundance is also affected by microbial cycling and in this specific case, ?36S /?33S? -7. Accordingly, ?33S-?36S co-variations can be used to discriminate distinct sedimentary pool. This contribution aims to test the robustness of MIF array of specific exospheric sulfur pools along their journey from the surface to the mantle. We examine the ?36S in addition to ?34S and ?33S signatures measured in-situ with secondary ion mass spectrometer, in sub lithospheric peridotitic and eclogitic sulfides from Kaapvaal (Jwaneng and Kimberley Pool) and Siberian craton (Mir and Udachnaya). Unlike peridotitic sulfides, eclogitic sulfides from both localities display significant MIF attesting from the presence of surficial sulfur in their source. More interestingly, the magnitude of the anomalies as well as ?36S/?33S ratio, differ from one locality to the other. Siberian eclogites match the composition of Eoarchean sulfate (?36S/?33S=-3 and ?33S<0‰). Sample from Jwaneng follow the MIF array previously reported in Archean chemical sediment (?36S/?33S=-1) while sulfide from Kimberley pool match the composition of some meso-Archean sediments in good agreement with isochron age reported in the literature for the sulfide from this locality. This study confirms that surficial sulfur has been efficiently transferred to the lithospheric mantle. More interestingly, it shows that peculiar sedimentary pools are still preserved in the cratonic keels.
Abstract: Archean supracrustal rocks (i.e. chemical sediments and metavolcanics) preserve sulfur Mass Independent Fractionations (MIF) that originate from photochemical reactions occurring in atmosphere before the great oxygenation event, 2.45 Ga. Reduced and oxidized aerosols were produced by photochemistry and respectively carry 33S enrichment (?33S > 0‰) and depletion (?33S < 0‰). The relative abundance of the minor isotope of sulfur (36S) was also affected by MIF in such a way that compact negative correlation exists between ?33S and ?36S. For much of Archean sediments, ?36S /?33S? -1, while slight variation of this slope have been attributed to minor change in the chemical composition of the atmosphere affecting global MIF source mechanism. On another hand, 36S abundance is also affected by microbial cycling and in this specific case, ?36S /?33S? -7. Accordingly, ?33S-?36S co-variations can be used to discriminate distinct sedimentary pool. This contribution aims to test the robustness of MIF array of specific exospheric sulfur pools along their journey from the surface to the mantle. We examine the ?36S in addition to ?34S and ?33S signatures measured in-situ with secondary ion mass spectrometer, in sub lithospheric peridotitic and eclogitic sulfides from Kaapvaal (Jwaneng and Kimberley Pool) and Siberian craton (Mir and Udachnaya). Unlike peridotitic sulfides, eclogitic sulfides from both localities display significant MIF attesting from the presence of surficial sulfur in their source. More interestingly, the magnitude of the anomalies as well as ?36S/?33S ratio, differ from one locality to the other. Siberian eclogites match the composition of Eoarchean sulfate (?36S/?33S=-3 and ?33S<0‰). Sample from Jwaneng follow the MIF array previously reported in Archean chemical sediment (?36S/?33S=-1) while sulfide from Kimberley pool match the composition of some meso-Archean sediments in good agreement with isochron age reported in the literature for the sulfide from this locality. This study confirms that surficial sulfur has been efficiently transferred to the lithospheric mantle. More interestingly, it shows that peculiar sedimentary pools are still preserved in the cratonic keels.
Abstract: Archean supracrustal rocks (i.e. chemical sediments and metavolcanics) preserve sulfur Mass Independent Fractionations (MIF) that originate from photochemical reactions occurring in atmosphere before the great oxygenation event, 2.45 Ga. Reduced and oxidized aerosols were produced by photochemistry and respectively carry 33S enrichment (?33S > 0‰) and depletion (?33S < 0‰). The relative abundance of the minor isotope of sulfur (36S) was also affected by MIF in such a way that compact negative correlation exists between ?33S and ?36S. For much of Archean sediments, ?36S /?33S? -1, while slight variation of this slope have been attributed to minor change in the chemical composition of the atmosphere affecting global MIF source mechanism. On another hand, 36S abundance is also affected by microbial cycling and in this specific case, ?36S /?33S? -7. Accordingly, ?33S-?36S co-variations can be used to discriminate distinct sedimentary pool. This contribution aims to test the robustness of MIF array of specific exospheric sulfur pools along their journey from the surface to the mantle. We examine the ?36S in addition to ?34S and ?33S signatures measured in-situ with secondary ion mass spectrometer, in sub lithospheric peridotitic and eclogitic sulfides from Kaapvaal (Jwaneng and Kimberley Pool) and Siberian craton (Mir and Udachnaya). Unlike peridotitic sulfides, eclogitic sulfides from both localities display significant MIF attesting from the presence of surficial sulfur in their source. More interestingly, the magnitude of the anomalies as well as ?36S/?33S ratio, differ from one locality to the other. Siberian eclogites match the composition of Eoarchean sulfate (?36S/?33S=-3 and ?33S<0‰). Sample from Jwaneng follow the MIF array previously reported in Archean chemical sediment (?36S/?33S=-1) while sulfide from Kimberley pool match the composition of some meso-Archean sediments in good agreement with isochron age reported in the literature for the sulfide from this locality. This study confirms that surficial sulfur has been efficiently transferred to the lithospheric mantle. More interestingly, it shows that peculiar sedimentary pools are still preserved in the cratonic keels.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0627-2 9p.
Africa, Botswana
deposit - Orapa
Abstract: This paper presents the results of an investigation into the structure of eolian kimberlite indicator minerals (KIMs) haloes present within Quaternary Kalahari Group sediments (up to 20 m thick) overlying the Late Cretaceous kimberlites in the Orapa field in North-East Botswana. A database of more than 8000 samples shows that kimberlites create a general mineralogical blanket of KIMs of various distances of transportation from primary sources in the Orapa area. Models of the reflection and dispersion patterns of KIMs derived from kimberlite pipes including AK10/ AK22/AK23 have been revealed based on 200 selected heavy mineral samples collected during diamond prospecting activities in Botswana from 2014 to 2017. Short distance eolian haloes situated close to kimberlite bodies cover gentle slopes within plains up to 500 × 1000 m in size. They have regularly have oval or conical shapes and are characterized by the presence mainly of unabraded or only slightly abraded KIMs. A sharp reduction of their concentration from hundreds and thousands of grains / 20 l immediately above kimberlites toto 10 grains/20 l at a distance of only 100-200 m from the pipes is a standard feature of these haloes. The variation of concentration, morphology and abrasion of specific KIMs with increasing distance from the primary sources has been investigated and presented herein. Sample volumes recommended for pipes present within a similar setting as those studied, with different depth of sedimentary cover are as follows: up to 10-20 m cover at 20-50 l, 20-30 m cover at 50-100 l and 30-80 m cover at 250 l. It is important to appreciate that the discovery of even single grains of unabraded or slightly abraded KIMs in eolian haloes are of high prospecting significance in this area. The results of the research can be applied to in diamond prospecting programs in various regions with similar environments.
Abstract: Kyanite-eclogite xenoliths from Wajrakarur are considered as remnants of subducted ocean-floor crust. Here trace element concentration and isotopic data are presented in garnet (Grt) and kyanite (Ky) from xenoliths KL-2 E1-E4, characterized by. We use the precise 87Sr/86Sr host kimberlite groundmass perovskite ratio (0.70312-0.70333, as a proxy for the extent of kimberlitic magma infiltration at 1.1 Ga. The xenolithic Grt and Cr-rich (upto 1506 ppm) Ky have more radiogenic 87Sr/86Sr values than kimberlite, at 1.1 Ga, of 0.703829-0.705203 and 0.703811-0.704502, respectively. Furthermore, the Grt and Ky 143Nd/144Nd ratios, at 1.1 Ga, are 0.509321-0.511372 and 0.510951-0.511156, respectively, and are distinctly lower than those of the host kimberlite (0.511870-0.512290). This indicates that the infiltration of kimberlitic fluid has not altered the 87Sr/86Sr and 143Nd/144Nd ratios in the Grt and Ky, and therefore their isotope compositions must be inherited and predate the kimberlite magma generation event at 1.1 Ga. Trace elements in Grt and Ky indicate extreme metasomatism (Sr in Grt 104-296 ppm, in Ky 672-8713 ppm [limit Sr<2ppm] and Nb in Grt 0.64-1.78 ppm, in Ky 1.7-4.54 ppm [limit Nb<0.5ppm]). The xenoliths underwent at least one major melting event inferred from extreme depletions in Re, Os and 177Os/178Os ratios [5]. Their mantle-like ?18O values (Grt 5.3-5.4‰, Ky 5.3-5.9‰), positive Eu anomalies in both Grt and Ky (similar to Group 1 HREE-depleted garnets of) suggests that the protolith likely was a chromite-bearing leucogabbro, emplaced as a high-pressure cumulate at the crust-mantle boundary, which was later eclogitized due to deep-seated subduction and underwent episodes of extreme melting and metasomatism before 1.1 Ga and at least before 1.7 Ga, as inferred from their youngest Re depletion dates.
Abstract: Mineral and fluid/melt inclusions in diamonds, which are encapsulated and isolated during a metasomatic event, offer the opportunity to constrain changes in the sub-continental lithospheric mantle that occurred during individual thermochemical events. Fibrous diamonds from the Group I De Beers Pool kimberlites, South Africa (SA), trapped incompatibleelement enriched saline high-density fluids (HDFs) and peridotitic mineral microinclusions. Their substitutional nitrogen resides almost exclusively in A-centers. With regard to the elevated thermal conditions that prevailed in the SA lithosphere during and following Karoo volcanism at ~180 Ma, this low-aggregation state of nitrogen suggests a short mantle residence time, constraining the time of saline metasomatism to be close to the eruption of the kimberlites at ~85 Ma. Thermometry of mineral microinclusions yield temperatures between 875-1080 ºC (at 5 GPa). These temperatures overlap with conditions recorded by touching inclusion pairs, which represent the mantle ambient conditions just before eruption, and are altogether lower by 150-250°C compared to P-T gradients recorded by peridotite xenoliths from the same locality. In addition, the oxygen fugacity calculated for the saline HDF compositions (?log??O2(FMQ) = -2.5 to -1.3) are higher by about a log unit compared with that recorded by xenoliths at 4-7 GPa. We conclude that enriched saline HDFs mediated the metasomatism that preceded Group I kimberlite eruptions in the southwestern Kaapvaal craton, and that their ‘cold and oxidized’ nature reflects their derivation from a deep subducting slab. To reconcile the temperature and oxygen fugacity discrepancy between inclusions in diamonds and xenoliths, we argue that xenoliths did not equilibrate during the last saline metasomatic event or kimberlite eruption. Thus the P-T-??O2 gradients they record express pre-existing lithospheric conditions that were likely established during the last major thermal event in the Kaapvaal craton (i.e. the Karoo magmatism at ca. 180 Ma).
Abstract: The Diavik Waste Rock Project, located in a region of continuous permafrost in northern Canada, includes complementary field and laboratory experiments with the purpose of investigating scale-up techniques for the assessment of the geochemical evolution of mine waste rock at a large scale. As part of the Diavik project, medium-scale field experiments (?1.5?m high active zone lysimeters) were conducted to assess the long term geochemical evolution and drainage of a low-sulfide waste rock under a relatively simple (i.e. constrained by the container) flow regime while exposed to atmospheric conditions. A conceptual model, including the most significant processes controlling the sulfide-mineral oxidation and weathering of the associated host minerals as observed in a laboratory humidity cell experiment, was developed as part of a previous modelling study. The current study investigated the efficacy of scaling the calibrated humidity cell model to simulate the geochemical evolution of the active zone lysimeter experiments. The humidity cell model was used to simulate the geochemical evolution of low-sulfide waste rock with S content of 0.053?wt.% and 0.035?wt.% (primarily pyrrhotite) in the active zone lysimeter experiments using the reactive transport code MIN3P. Water flow through the lysimeters was simulated using temporally variable infiltration estimated from precipitation measurements made within 200?m of the lysimeters. Flow parameters and physical properties determined during previous studies at Diavik were incorporated into the simulations to reproduce the flow regime. The geochemical evolution of the waste-rock system was simulated by adjustment of the sulfide-mineral content to reflect the values measured at the lysimeters. The temperature dependence of the geochemical system was considered using temperature measurements taken daily, adjacent to the lysimeters, to correct weathering rates according to the Arrhenius equation. The lysimeter simulations indicated that a model developed from simulations of laboratory humidity cell experiments, incorporating detailed representations of temporally variable temperature and water infiltration, can be scaled to provide a reasonable assessment of geochemical evolution of the medium-scale field experiments.
Abstract: The geochemical evolution of mine-waste rock often includes concurrent acid generation and neutralization processes. Deposition of mine-waste rock in large, oxygenated, and partially saturated piles can result in release of metals and decreased pH from weathering of sulfide minerals. Acid neutralization processes can often mitigate metals and pH impacts associated with sulfide oxidation. The Diavik Waste Rock Project included large field experiments (test piles built in 2006) conducted to characterize weathering of sulfide waste rock at a scale representative of full size waste-rock piles. Water samples from the unsaturated interior of one of the test piles, constructed of waste rock with ~0.05 wt.% S, were collected using soil water solution samplers and drains at the base of the pile. Field observations indicated pH decreased throughout the depth of the pile during 2008 and 2009 and that carbonate mineral buffering was entirely depleted by 2011 or 2012. Carbonate mineral exhaustion was accompanied by increased concentrations of dissolved Al and Fe in effluent samples collected at the basal drains. These results suggest that dissolution of Al and Fe(oxy)hydroxides occurred after the depletion of carbonate minerals following an acid neutralization sequence that is similar to observations made by previous researchers. A conceptual model of acid neutralization proceses within the pile, developed using physical and geochemical measurements conducted from 2008 to 2012, was used to inform reactive transport simulations conducted in 2017 to quantify the dominant acid neutralization processes within the test pile interior. Reactive transport simulations indicate that the conceptual model developed using the results of field samples provides a reasonable assessment of the evolution of the acid neutralization sequence.
Abstract: Zircon xenocrysts from the kimberlites offer a unique opportunity to identify the cryptic basement components hidden in the deep crust and thus to image lithospheric structure and crustal evolution. Zircon xenocrysts from the Triassic kimberlites, exposed in the Rangrim massif of North Korea, were selected for in situ U-Pb and Hf analyses. These zircon xenocrysts are all crust-derived. Their U-Pb age spectrum is characterized by one prominent age population at ca. 1.9-1.8 Ga without any Archean ages, indicating a Paleoproterozoic-dominated basement in the depth of the Rangrim massif. Archean basement should be very limited or absent at depth. This is different with the previous thought of the Rangrim massif being an Archean terrane. However, most of those Paleoproterozoic zircons display negative ?Hf(t) values (-9.7~+0.7) with the average Hf model age of 2.83 ± 0.09 Ga (2?), implying that protoliths of those zircons were not juvenile but derived from reworking of the pre-existed Archean basement. These observations argue for a strong crustal reworking event occurred in the Rangriam massif during Paleoproterozoic, which exhausted most of the preexisted Archean basement rocks and generated a large abundance of Paleoproterozoic rocks. The 1.9~1.8 Ga thermal event has been well documented in the adjacent Jiao- Liao-Ji orogenic belt of the North China Craton. Both of them are characterized by the widely distributed 1.9~1.8 Ga magmatism and share similar igneous rock assemblage. We suggest that the Rangrim massif may be the eastern extension of the Jiao-Liao-Ji belt in North Korea, constituting part of a huge Paleoproterozoic orogen in the eastern margin of the Sino-Korean craton.
Journal of African Earth Sciences, Vol. 147, pp. 374-382.
Africa, Tanzania
deposit - Oldoinyo Lengai
Abstract: The northern Tanzanian sector of the Gregory Rift is an area of an active continental rifting, in which sedimentation processes are strongly affected by volcanism. Due to limited stratigraphic exposure, the volcanic record of the region is rather sparse, and assigning volcanic centres for the individual eruptions is difficult. This study presents new data on the tephrostratigraphy of the sedimentary sequence of Lake Emakat, Empakaai Crater, northern Tanzania. Seven volcanic ash layers are identified and described from a 1.1-m core of lake sediments. Geochemical, mineralogical, petrographic and magnetic analyses show that: (1) all ash layers are products of highly explosive eruptions of melilite-bearing magmas; (2) most of the eruptions originate from a complex magmatic system; (3) all ash horizons are very well preserved in the lake environment; and (4) there are significant fluctuations of the bulk magnetic susceptibility of the lacustrine sediments which is related to microtephra from additional eruptions, the result of detritus, washed from the shore during periods of strong lake level fluctuations or periods of high erosion rates, or simply by the contamination by the material from the ash layers. Based on geochemistry and mineralogy of the seven identified ash layers in Lake Emakat, combined with the eruption ages from ¹?C datings, we can pinpoint Oldoinyo Lengai volcano as the source of these specific layers. The combination of this new data with existing chronological data from Ryner et al. (2007), retrieved from the same core, provides precise ages of the voluminous highly explosive eruptions in this region of East Africa during the Pleistocene-Holocene transition.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0631-6 13p.
Canada, Northwest Territories
deposit - Kelvin
Abstract: The early Cambrian to late Neoproterozoic Kelvin kimberlite pipe is located in the southeast of the Archean Slave Craton in northern Canada, eight km northeast of the Gahcho Kué diamond mine. Kelvin was first discovered in 2000 by De Beers Canada. Subsequent exploration undertaken by Kennady Diamonds Inc. between 2012 and 2016 resulted in the discovery of significant thicknesses of volcaniclastic kimberlite that had not previously been observed. Through extensive delineation drilling Kelvin has been shown to present an atypical, steep-sided inclined L-shaped pipe-like morphology with an overall dip of 15 to 20°. With a surface expression of only 0.08 ha Kelvin dips towards the northwest before turning north. The body (which remains open at depth) has been constrained to a current overall strike length of 700 m with varying vertical thickness (70 to 200 m) and width (30 to 70 m). Detailed core logging, petrography and microdiamond analysis have shown that the pipe infill comprises several phases of sub-horizontally oriented kimberlite (KIMB1, KIMB2, KIMB3, KIMB4, KIMB7 and KIMB8) resulting from multiple emplacement events. The pipe infill is dominated by Kimberley-type pyroclastic kimberlite or “KPK”, historically referred to as tuffisitic kimberlite breccia or “TKB”, with less common hypabyssal kimberlite (HK) and minor units with textures transitional between these end-members. An extensive HK sheet complex surrounds the pipe. The emplacement of Kelvin is believed to have been initiated by intrusion of this early sheet system. The main pipe-forming event and formation of the dominant KPK pipe infill, KIMB3, was followed by late stage emplacement of additional minor KPK and a hypabyssal to transitional-textured phase along the upper contact of the pipe, cross-cutting the underlying KIMB3. Rb-Sr age dating of phlogopite from a late stage phase has established model ages of 531 ± 8 Ma and 546 ± 8 Ma. Texturally and mineralogically, the Kelvin kimberlite is similar to other KPK systems such as the Gahcho Kué kimberlites and many southern African kimberlites; however, the external morphology, specifically the sub-horizontal inclination of the pipe, is unique. The morphology of Kelvin and the other kimberlites in the Kelvin-Faraday cluster defines a new type of exploration target, one that is likely not unique to the Kennady North Project area. Extensive evaluation work by Kennady Diamonds Inc. has resulted in definition of a maiden Indicated Mineral Resource for Kelvin of 8.5 million tonnes (Mt) of kimberlite at an average grade of 1.6 carats per tonne (cpt) with an average diamond value of US$ 63 per carat (ct).
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0634-3 12p.
Africa, Botswana
deposit - Jwaneng
Abstract: To fully understand the implications of the compositional information recorded by inclusions in diamond it is vital to know if their growth was syn- or protogenetic and the extent to which they have equilibrated with diamond forming agents. The current paradigm is that the majority of inclusions in diamond are syngenetic but recently this assumption has been questioned. This study presents an integrated cathodoluminescence (CL) and electron backscatter diffraction (EBSD) study of 8 diamonds containing eclogitic inclusions: 19 pyrope-almandine garnets, 12 omphacitic clinopyroxenes, 4 sulphides, 1 coesite and 1 rutile from the Jwaneng diamond mine, Botswana. Diamond plates were sequentially polished to expose inclusions at different levels and CL imaging and EBSD were performed to constrain the relationship between diamond and inclusion growth. Despite complex growth and resorption, individual diamonds are single crystals with a homogeneous crystallographic orientation. All individual inclusions have homogeneous crystallographic orientation and no resolvable compositional zonation. The combined CL and EBSD data suggest that epitaxial inclusion-diamond growth is rare (none of 24 inclusions) and that the imposition of cubo-octahedral faces on inclusions does not necessarily result in epitaxy. Individual diamonds contain inclusions that record evidence of both syngentic and protogenetic relationships with the host diamond and in one case an inclusion appears syngenetic to the diamond core but protogenetic to the growth zone that surrounds 70% of the inclusion. These findings emphasise that inclusions in diamonds have multiple modes of origin and that in order to validate the significance of geochronological studies, further work is needed to establish that there is rapid chemical equilibration of protogenetic inclusions with diamond forming agents at mantle temperatures.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0633-4 13p.
Canada, Quebec
deposit - Renard
Abstract: Renard 65, a diamondiferous pipe in the Neoproterozoic Renard kimberlite cluster (Québec, Canada), is a steeply-dipping and downward-tapering diatreme comprised of three pipe-filling units: kimb65a, kimb65b, and kimb65d. The pipe is surrounded by a marginal and variably-brecciated country rock aureole and is crosscut by numerous hypabyssal dykes: kimb65c. Extensive petrographic and mineralogical characterization of over 700 m of drill core from four separate drill holes, suggests that Renard 65 is a Group I kimberlite, mineralogically classified as phlogopite kimberlite and serpentine-phlogopite kimberlite. Kimb65a is a massive volcaniclastic kimberlite dominated by lithic clasts, magmaclasts, and discrete olivine macrocrysts, hosted within a fine-grained diopside and serpentine-rich matrix. Kimb65b is massive, macrocrystic, coherent kimberlite with a groundmass assemblage of phlogopite, spinel, perovskite, apatite, calcite, serpentine and rare monticellite. Kimb65c is a massive, macrocrystic, hypabyssal kimberlite with a groundmass assemblage of phlogopite, serpentine, calcite, perovskite, spinel, and apatite. Kimb65d is massive volcaniclastic kimberlite with localized textures that are intermediate between volcaniclastic and coherent, with tightly packed magmaclasts separated by a diopside- and serpentine-rich matrix. Lithic clasts of granite-gneiss in kimb65a are weakly reacted, with partial melting of feldspars and crystallization of richterite and actinolite. Lithic clasts in kimb65b and kimb65d are entirely recrystallized to calcite + serpentine/chlorite + pectolite and display inner coronas of diopside-aegirine and an outer corona of phlogopite. Compositions are reported for all minerals in the groundmass of coherent kimberlites, magmaclasts, interclast matrices, and reacted lithic clasts. The Renard 65 rocks are texturally classified as Kimberley-type pyroclastic kimberlites and display transitional textures. The kimberlite units are interpreted to have formed in three melt batches based on their distinct spinel chemistry: kimb65a, kimb65b and kimb65d. We note a strong correlation between the modal abundances of lithic clasts and the textures of the kimberlites, where increasing modal abundances of granite/gneiss are observed in kimberlites with increasingly fragmental textures.
Abstract: Olivine phenocryst chemistry is a useful tracer of mantle source lithology as olivine is typically the first mineral to crystallize in a range of mafic to alkaline magma types and contains geochemical information about the primary parent magma composition. It is particularly useful in discriminating between pyroxenite (i.e.,recycled crustal component) and peridotite mantle source lithologies. Radiogenic isotope studies of HIMU basalts have shown the important role of a recycled crustal component in the source. However, olivine chemistry of HIMU basalts suggests a dominantly peridotitic mantle source with a subduction-derived metasomatic carbonate component. To further investigate how olivine chemistry can be used to understand the source of HIMU magmas, I present major and trace element data for olivine megacrysts related to the 89?Ma Cr-poor megacryst suite from the Monastery kimberlite (South Africa), which have previously been interpreted to crystallize at high P-T conditions of ~1400?°C and ~5?GPa from a magma sourced from a HIMU reservoir. Olivine megacrysts have high-Ni concentrations at a given Fo (forsterite) content, overlapping ocean island basalts (OIB) interpreted to have formed from pyroxenite-dominated sources but are distinct from typical olivine in HIMU basalts. However, they have low 100*Mn/Fe (0.8-1.1) and no correlation is observed between Ni and trace elements indicative of recycled components such as Co, Li, or Zn. The olivine megacryst chemistry is similar to that of aillikite olivine interpreted to be controlled by phlogopite in the source rather than pyroxenite. Comparison with olivine chemistry from orangeites/Group II kimberlites (sourced from phlogopite-rich mantle lithologies) supports a phlogopite controlon low 100*Mn/Fe in olivine. Further comparison with olivine phenocryst chemistry of HIMU melilitites (76-58?Ma) in southern Africa suggests a mineralogically heterogeneous HIMU reservoir formed by metasomatic modification of the lithospheric mantle in southern Africa. Thus, olivine megacryst chemistry supports interpretations for the recycled component of the HIMU reservoir as mineralogically complex metasomatic lithologies formed by the infiltration of subduction-derived melts into the base of the lithospheric mantle. In addition to carbonate-richHIMU mantle lithologies in southern Africa and worldwide, Monastery kimberlite olivine megacrysts and olivine in melilitites suggest that a phlogopite-richHIMU lithology is present in southern Africa. An important question arising from this study is in reconciling the homogenous isotopic ratios of HIMU basalts worldwide with an apparent heterogeneous lithological source indicated by olivine chemistry.
Abstract: The flux of elements into Earth's sub-continental lithospheric mantle is facilitated by the passage of small-fraction melts that either crystallise new phases or react with pre-existing minerals.Metasomatised peridotite records the end product of this exchange but rarely captures the process in the act due to subsolidus re-equilibration. We present the results of a systematic investigation of a metasomatic melt channel preserved in a mantle peridotite from the Late Cretaceous Bultfontein kimberlite (Kaapvaal craton) that shows rare direct evidence of the melt-rock reaction processes. We show that the metasomatic proto-kimberlite melt underwent variable crystallisation of clinopyroxene, sulfides, phlogopite, spinel and zircon together with interaction and diffusive exchange with the surrounding olivine-rich mantle. Element profiles across large olivine porphyroclasts (Fo88) show significant core-to-rim variations in Ni (NiO?=?0.18-0.32?wt%) and Cr (Cr?=?35-60?ppm), while concentrations of all other elements (e.g. Mg, Fe, Mn, Co, V)are remarkably homogeneous. Electron backscatter diffraction analysis shows that the disequilibrium of Ni and Cr is greatest where the crystal contains large components of the [100] and [010] axes. The disequilibrium is preserved in certain orientations because diffusion of Ni and Cr in olivine is more anisotropic than Fe-Mg and Mn, and slower in the [100] and [010] directions. We present the first observations of Ni and Cr decoupling from other elements in mantle olivine and suggest that this is a consequence of: (i)changing mineral-melt concentration gradients associated with the reactive percolation of a precursory kimberlite melt; and (ii) late-stage sulfide and spinel precipitation. We use the diffusion limited re-equilibration of Ni in olivine to quantify the timing of metasomatism prior to xenolith entrainment by the host kimberlite. Our modelling indicates that reactive percolation occurred on the order of 103-105?years prior to entrainment; this provides an additional line of support for the hypothesis that a period of metasomatism by proto-kimberlite melts precedes the final kimberlite ascent to the surface. The broader implication of our finding of variable rates of minor element diffusion in natural olivine is that it highlights the importance of anisotropy and the impact of changing local concentration gradients during subsolidus re-equilibration.
Russian Geology and Geophysics, Vol. 59, 7, pp. 763-779.
Russia, Siberia
deposit - Udachnaya
Abstract: A comprehensive study of 26 mafic mantle xenoliths from the Udachnaya kimberlite pipe was carried out. The contents of major and trace elements, equilibrium temperature parameters, and water content in the rock-forming minerals were determined. The temperatures of formation of the studied rocks are estimated at 800-1300 °C. According to IR spectroscopy data, the water content in clinopyroxenes from the studied eclogites varies from values below the detection limit to 99 ppm. The IR spectra of garnets lack bands of water. The water content in clinopyroxene and orthopyroxene from garnet websterite is 72 and 8 ppm, respectively. The water content in the average rock, calculated from the ratio of the rock-forming minerals, varies from a few to 55 ppm. No relationship among the water content, equilibrium temperatures, and rock composition is established. The low water contents in the eclogites are close to the earlier determined water contents in peridotites from the same pipe and are, most likely, due to the re-equilibration of the eclogites with the rocks of the peridotitic lithospheric mantle. The dehydration of the protolith during its subduction and the partial melting of eclogites before their removal by kimberlitic magma to the surface might be an additional cause of the low water contents in the mantle eclogite xenoliths.
Abstract: Geophysical imaging of trans-lithospheric structures provide a spatial link between ore deposits in the crust and the underlying cratonic mantle. However, the deep lithosphere's role in ore deposit genesis remains poorly understood because remotely acquired datasets do not provide any direct constraints on the behaviour of ore elements within these mantle-roots. The abundance and behaviour of ore elements governs the metallic endowment of the cratonic mantle and the economic potential of mantle-derived magmas. Herein we present in situ electron probe microanalysis (EPMA) and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) geochemical datasets for clinopyroxene and olivine mantle xenocrysts from the Jurassic Kirkland Lake kimberlite field, Abitibi greenstone belt, Canada. We specifically focus on unconventional trace elements, including ore elements with chalcophile and/or siderophile affinities (Ag-As-Au-Bi-Cu-Mo-Pb-Pt-Pd-Sb-Se-Sn-Te-W-Zn). Robust principal component analysis suggests that low-T, large-ion lithophile element alteration (Ba-Sr), which likely occurred during kimberlite emplacement, represents the largest source of variance for the xenocryst dataset. PT-dependent element partitioning during sub-solidus equilibration represents the second most important control on olivine and clinopyroxene chemistry. We demonstrate that least-altered, high-PT mantle silicates are, in fact, a significant mineral host for a range of ore elements (Cu-Zn ± Ag ± As ± Se ± Sn ± Mo) within equilibrated, garnet peridotite at depth (70-190 km). Statistical analysis of the raw, individual mass sweeps for each LA-ICP-MS signal suggest that the most abundant ore elements (Cu-Zn) occur predominantly as PT-dependent substitution reactions with the dominant mineral-forming elements, rather than as inclusions. A subset of high-PT olivine (160-180 km) yields Fe-Ni-S-poor and Na (Au ± Pt ± Pd)-rich compositions, which may reflect metasomatism, sulphide segregation and trapping of precious metal-bearing fluids at the base of the lithosphere. These anomalous mantle fragments possibly represent the first, direct sampling of precious metal-modified mantle peridotite beneath the Abitibi. Mid-PT olivine xenocrysts (70-120 km), which yield Mg-rich and high field-strength element-poor compositions, document a highly melt-depleted segment of mantle peridotite coincident with and below a shallow-dipping, low-seismic-velocity anomaly and conductive feature of the Kirkland Lake mid-lithosphere at 70-100 km. We speculate that the trace element signature of mid-PT xenocrysts documents the re-distribution of high-charge and incompatible elements from refractory garnet peridotite to phlogopite- and/or amphibole-bearing peridotite with conductive metasomatic up-flow zones. The rapid, sub-solidus diffusion of elements at high-T suggest that these processes likely occurred during, and/or immediately preceding, kimberlite volcanism. New in situ Pb isotope analyses of clinopyroxene xenocrysts sampled from metasomatized, low-Al garnet peridotite, however, also document ancient metasomatic events that likely pre-date Jurassic kimberlitic volcanism by at least one billion years.
Geochemistry International, Vol. 56, 9, pp. 881-900.
Russia
deposit - Nyurbinskaya
Abstract: Interaction between a melt of kimberlite from the Nyurbinskaya pipe (Yakutia) and natural monocrystalline diamonds was studied experimentally at 0.15 GPa and 1200-1250°C in high-pressure and high-temperature Ar gas “bombs.” The loss of diamond weight with slight surface dissolution of diamonds in a Ca carbonate-bearing kimberlite melt over the course of 2 h (the period of kimberlite transport from upper-mantle diamond-forming chambers to the crustal cumulative centers) is 3-4.5%. In 4 and 7-8 days (under the conditions of crustal cumulative centers), the weight of diamond decreases with remarkable bulk dissolution by 13.5 and 24.5-27.5%, respectively. In the run at 0.15 GPa and 1200°C kimberlite and ilmenite (added) melts interact to produce perovskite melt. Both of the melts, rich in titanium minerals, are immiscible with kimberlite melt and therefore cannot influence the diamond dissolution kinetics in the kimberlite melt. The experimental results suggest that precisely the dissolution processes for thermodynamically metastable diamonds in silicate-carbonate kimberlitic magmas are responsible for the effective decrease in the diamond potential of kimberlite deposits. The paper discusses the physicochemical reasons for the decrease in the kimberlite diamond potential during the chemically active history of diamond genesis: from upper-mantle chambers to the explosive release of diamonds and kimberlite material from cumulative centers to the Earth’s surface. The data on experimental physicochemical studies of the origin, analytical mineralogy of inclusions, and isotope geochemistry of diamonds are correlated.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0630-7 14p.
Canada, Northwest Territories
deposit - Diavik
Abstract: The Diavik Diamond Mine in the NWT of Canada has produced in excess of 100 million carats from 3 kimberlite pipes since mining commenced in 2002. Here, we present new findings from deep (>400 m below surface) mining, sampling and drilling work in the A154N kimberlite volcano that require a revision of previous geological and emplacement models and provide a window into how the sub-continental lithospheric mantle (SCLM) below Diavik was sampled by kimberlite magmas through time. Updated internal geological models feature two volcanic packages interpreted to represent two successive cycles of explosive eruption followed by active and passive sedimentation from a presumed crater-rim, both preceded and followed by intrusions of coherent kimberlite. Contact relationships apparent among the geological units allow for a sequential organization of as many as five temporally-discrete emplacement events. Representative populations of mantle minerals extracted from geological units corresponding to four of the emplacement events at A154N are analyzed for major and trace elements, and provide insights into the whether or not kimberlites randomly sample from the mantle. Two independent geothermometers using clinopyroxene and garnet data indicate similar source depths for clinopyroxenes and G9 garnets (130-160 km), and suggest deeper sampling with time for both clinopyroxene and garnets. Harzburgite is limited to 110-160 km, and appears more prevalent in early, low-volume events. Variable ratios of garnet parageneses from the same depth horizons suggest random sampling by passing magmas, but deeper garnet sampling through time suggests early preferential sampling of shallow/depleted SCLM. Evaluations of Ti, Zr, Y and Ga over the range of estimated depths support models of the SCLM underlying the central Slave terrane.
History of Photography, Vol. 42, 1, pp. 4-24. doi.org/10.1080/ 03087298.2018. 1429095
Africa, South Africa
deposit - Kimberley
Abstract: In the mid 1880s a little-known photographer named Robert Harris produced a series of albumen prints showing the stages of body searching that black labourers in De Beers diamond mines were obliged to undergo by state ordinance enacted in 1883. The original photographs surfaced briefly in the saleroom in 2007 but have since disappeared. Two sets of copies survive. Bearing in mind the history of documentary photography in South Africa, this article examines the historical and textual significance of this series of photographs in the context of the history of mining and discusses the imperatives and ethics of locating, researching, and publishing controversial imagery in the Internet age.
Mineralogy and Petrology, doi.org/101007/ s00710-018-0629-0 13p.
Canada, Quebec
deposit - Renard
Abstract: Kimberlites are rare volatile-rich ultramafic magmas thought to erupt in short periods of time (<1 Myr) but there is a growing body of evidence that the emplacement history of a kimberlite can be significantly more protracted. In this study we report a detailed geochronology investigation of a single kimberlite pipe from the Renard cluster in north-central Québec. Ten new high precision ID-TIMS (isotope dilution - thermal ionization mass spectrometry) U-Pb groundmass perovskite dates from the main pipe-infilling kimberlites and several small hypabyssal kimberlites from the Renard 2 pipe indicate kimberlite magmatism lasted at least ~20 Myr. Two samples of the main pipe-infilling kimberlites yield identical weighted mean 206Pb/238U perovskite dates with a composite date of 643.8?±?1.0 Myr, interpreted to be the best estimate for main pipe emplacement. In contrast, six hypabyssal kimberlite samples yielded a range of weighted mean 206Pb/238U perovskite dates between ~652-632 Myr. Multiple dates determined from these early-, syn- and late-stage small hypabyssal kimberlites in the Renard 2 pipe demonstrate this rock type (commonly used to date kimberlites) help to constrain the duration of kimberlite intrusion history within a pipe but do not necessarily reliably record the emplacement age of the main diatreme in the Renard cluster. Our results provide the first robust geochronological data on a single kimberlite that confirms the field relationships initially observed by Wagner (1914) and Clement (1982); the presence of antecedent (diatreme precursor) intrusions, contemporaneous (syn-diatreme) intrusions, and consequent (post-diatreme) cross-cutting intrusions. The results of this detailed U-Pb geochronology study indicate a single kimberlite pipe can record millions of years of magmatism, much longer than previously thought from the classical viewpoint of a rapid and short-duration emplacement history.
Contributions to Mineralogy and Petrology, Vol. 173, pp. 76- doi.org/10.1007/ s00410-018-1502-1
Africa, Lesotho
deposit - Letseng
Abstract: The Letšeng-la-Terae kimberlite (Lesotho), famous for its large high-value diamonds, has five distinct phases that are mined in a Main and a Satellite pipe. These diatreme phases are heavily altered but parts of a directly adjacent kimberlite blow are exceptionally fresh. The blow groundmass consists of preserved primary olivine with Fo86?88, chromite, magnesio-ulvöspinel and magnetite, perovskite, monticellite, occasional Sr-rich carbonate, phlogopite, apatite, calcite and serpentine. The bulk composition of the groundmass, extracted by micro-drilling, yields 24-26 wt% SiO2, 20-21 wt% MgO, 16-19 wt% CaO and 1.9-2.1 wt% K2O, the latter being retained in phlogopite. Without a proper mineral host, groundmass Na2O is only 0.09-0.16 wt%. However, Na-rich K-richterite observed in orthopyroxene coronae allows to reconstruct a parent melt Na2O content of 3.5-5 wt%, an amount similar to that of highly undersaturated primitive ocean island basanites. The groundmass contains 10-12 wt% CO2, H2O is estimated to 4-5 wt%, but volatiles and alkalis were considerably reduced by degassing. Mg# of 77.9 and 530 ppm Ni are in equilibrium with olivine phenocrysts, characterize the parent melt and are not due to olivine fractionation. 87Sr/86Sr(i)?=?0.703602-0.703656, 143Nd/144Nd(i)?=?0.512660 and 176Hf/177Hf(i)?=?0.282677-0.282679 indicate that the Letšeng kimberlite originates from the convective upper mantle. U-Pb dating of groundmass perovskite reveals an emplacement age of 85.5?±?0.3 (2?) Ma, which is significantly younger than previously proposed for the Letšeng kimberlite.
The Southern African Institute of Mining and Metallurgy Diamonds - from source to use 2013, 9p. Pdf researchgate
Africa, Angola, South Africa
deposit - Mulepe, Voorspoed
Abstract: Construction of geological models for kimberlites has historically largely been based on visual volcanic textures and features, with chemical data only produced on an ad-hoc basis depending on the level of perceived complexity observed in the geological data. The focus of this manuscript is a high-level mineral resource management view of the impact which the initial absence of proper chemical data had on two kimberlite resource models as well as the increasing magnitude of the problem caused by the lack of chemical data once the resource estimation process commenced. The impact of the absence of chemical data on projects where micro-diamond estimation techniques are employed is also discussed. Metallurgical parameters have historically not been incorporated into kimberlite resource models, but recent work at De Beers Group Services has shown that geostatistical quantification of the DMS (Dense Media Separator) yield is useful for mine planning purposes, and will add value in the understanding of the kimberlite emplacement process. A case study is presented where a geostatistical analysis and conditional simulation was performed on the DMS yield in a kimberlite at a local block scale. These data were used to identify mining blocks where the DMS yield would exceed the capability of the treatment plant.
The Southern African Institute of Mining and Metallurgy Diamonds - from source to use 2013, 9p. Pdf researchgate
Africa, Angola, South Africa
deposit - Mulepe, Voorspoed
Abstract: Construction of geological models for kimberlites has historically largely been based on visual volcanic textures and features, with chemical data only produced on an ad-hoc basis depending on the level of perceived complexity observed in the geological data. The focus of this manuscript is a high-level mineral resource management view of the impact which the initial absence of proper chemical data had on two kimberlite resource models as well as the increasing magnitude of the problem caused by the lack of chemical data once the resource estimation process commenced. The impact of the absence of chemical data on projects where micro-diamond estimation techniques are employed is also discussed. Metallurgical parameters have historically not been incorporated into kimberlite resource models, but recent work at De Beers Group Services has shown that geostatistical quantification of the DMS (Dense Media Separator) yield is useful for mine planning purposes, and will add value in the understanding of the kimberlite emplacement process. A case study is presented where a geostatistical analysis and conditional simulation was performed on the DMS yield in a kimberlite at a local block scale. These data were used to identify mining blocks where the DMS yield would exceed the capability of the treatment plant.
The Australian Gemmologist, Vol. 26, 9-10. p. 249.
Australia
deposit - Argyle
Abstract: Many kimberlite ore bodies are relatively small, and the presence of overburden along with the complexities of interpreting geophysical data can make it challenging to intersect a kimberlite target during exploration drilling. However, the analysis of country rock drill core from the perimeter of several known kimberlites provides evidence that subtle alteration (hydration) halos around kimberlites exist, which can be detected using rapid and cost-effective spectroscopic techniques. Identification of these hydration halos, which are independent of country rock composition, may provide crucial information about the presence of undiscovered kimberlite in an exploration area, especially if kimberlite was not intersected during initial drilling. Preliminary estimates suggest that these hydration halos, which are most likely caused by kimberlite-derived hydrous fluids, can extend more than 65 meters into the country rocks, but their size strongly depends on the size of the kimberlite body. Narrow kimberlite dikes produce much smaller halos compared to large kimberlite pipes. In addition, hydration halos in carbonate rocks appear to be smaller compared to silicate rocks .
Journal of the Geological Society of India, Vol. 92, 2, pp. 141-144.
India
deposit - Amba Dongar
Abstract: In the Amba Dongar diatreme, "ferrocarbonatite" is not a single unit of late differentiate of calciocarbonatite magma but it is a family with variation on field occurrence, mineralogy and chemistry of each unit. The family includes dikes of ankeritic carbonatites (phase I and II), plugs of ankeritic carbonatite within sövite ring dike, dikes of sideritic carbonatite in ankeritic carbonatite plug and rödberg veins. Their intrusive relations are very clear in the field and each phase has characteristic mineralogy and trace and REE geochemistry. According to the nomenclature suggested by Harmer and Gittins (1997) majority of "ferrocarbonatites" of Amba Dongar plot in field of "ferruginous calciocarbonatite" and only siderite and rödberg plot in the field of "ferrocarbonatite". Within these family members, their trace and REE show clear increase from early phase to last phase of sideritic carbonatite. The present short communication discusses various aspects of "ferrocarbonatites".
Abstract: The petrologically unique Udachnaya-East kimberlite (Siberia, Russia) is characterised by unserpentinised and H2O-poor volcaniclastic and coherent units that contain fresh olivine, along with abundant alkali-rich carbonates, chlorides, sulphides and sulphates in the groundmass. These mineralogical and geochemical characteristics have led to two divergent models that advocate different origins. It has been suggested that the unserpentinised units from Udachnaya-East are representative of pristine unaltered kimberlite. Conversely, the alkali-chlorine-sulphur enrichment has been attributed to interactions with crustal materials and/or post-emplacement contamination by brines. The mineralogical and geochemical features and the compositions of melt inclusions in unserpentinised and serpentinised Udachnaya-East kimberlite varieties are compared in this study. Both varieties of kimberlite have similar major, compatible and incompatible trace element concentrations and primitive mantle normalised trace element patterns, groundmass textures and silicate, oxide and sulphide mineral compositions. However, these two kimberlite varieties are distinguished by: (i) the presence of unaltered olivine, abundant Na-K-Cl-S-rich minerals (i.e. chlorides, S-bearing alkali-carbonates, sodalite) and the absence of H2O-rich phases (i.e. serpentine, iowaite (Mg4Fe3+(OH)8OCl•3(H2O)) in unserpentinised samples, and (ii) the absence of alkali- and chlorine-enriched phases in the groundmass and characteristic olivine alteration (i.e. replacement by serpentine and/or iowaite) in serpentinised samples. In addition, melt inclusions hosted in olivine, monticellite, spinel and perovskite from unserpentinised and serpentinised kimberlite contain identical daughter phase assemblages that are dominated by alkali-carbonates, chlorides and sulphates/sulphides. This enrichment in alkalis, chlorine and sulphur in melt inclusions demonstrates that these elements were an intrinsic part of the parental magma. The paucity of alkali-carbonates and chlorides in the groundmass of serpentinised Udachnaya-East kimberlite is attributed to their instability and removal during post-emplacement alteration. All evidence previously used in support of crustal and brine contamination of the Udachnaya-East kimberlite is thoroughly evaluated. We demonstrate that ‘contamination models’ are inconsistent with petrographic, geochemical and melt inclusion data. Our combined data suggest that the Udachnaya-East kimberlite crystallised from an essentially H2O-poor, Si-Na-K-Cl-S-bearing carbonate-rich melt.
Doklady Earth Sciences, Vol. 482, 1, pp. 1130-1133.
Russia
deposit - Lake Kimozero
Abstract: Syngenetic and epigenetic ore mineralization was studied in Paleoproterozoic metakimberlites in the area of Kimozero Lake. In the Kimozero structure, redeposited ore mineralization is constrained to fracture and shear zones and consists of Fe-vaesite, Fe-Co-polydymite, millerite, Ni-pyrrhotite, pentlandite, chalcopyrite, Zn-bearing copper, galena, and Ni-pyrite. The composition of this mineralization is analogous to that of syngenetic mineralization in pyroclastic and coherent kimberlite, and its likely source was the kimberlite itself.
Journal of African Earth Sciences, Vol. 137, pp. 9-21.
Africa, Botswana
deposit - Jwaneng
Abstract: Country rock at Jwaneng Diamond Mine provides a rare insight into the deformational history of the Transvaal Supergroup in southern Botswana. The ca. 235 Ma kimberlite diatremes intruded into late Archaean to Early Proterozoic, mixed, siliciclastic-carbonate sediments, that were subjected to at least three deformational events. The first deformational event (D1), caused by NW-SE directed compression, is responsible for NE-trending, open folds (F1) with associated diverging, fanning, axial planar cleavage. The second deformational event (D2) is probably progressive, involving a clockwise rotation of the principal stress to NE-SW trends. Early D2, which was N-S directed, involved left-lateral, oblique shearing along cleavage planes that developed around F1 folds, along with the development of antithetic structures. Progressive clockwise rotation of far-field forces saw the development of NW-trending folds (F2) and its associated, weak, axial planar cleavage. D3 is an extensional event in which normal faulting, along pre-existing cleavage planes, created a series of rhomboid-shaped, fault-bounded blocks. Normal faults, which bound these blocks, are the dominant structures at Jwaneng Mine. Combined with block rotation and NW-dipping bedding, a horst-like structure on the northwestern limb of a broad, gentle, NE-trending anticline is indicated. The early compressional and subsequent extensional events are consistent throughout the Jwaneng-Ramotswa-Lobatse-Thabazimbi area, suggesting that a large area records the same fault geometry and, consequently, deformational history. It is proposed that Jwaneng Mine is at or near the northernmost limit of the initial, northwards-directed compressional event.
Diamond & Related Materials, Vol. 89, pp. 322-329.
Russia, India
deposit - Mir, Panna
Abstract: The optical features of milky type IaB diamonds were studied systematically by non-destructive approaches including FTIR, photoluminescence (PL), and cathodoluminescence (CL) spectroscopy. From 97 type IaB diamonds ranging from 0.2?ct to ~100?ct submitted to GIA's New York laboratory for screening, we found that all the milky type IaB diamonds consistently displayed the hydrogen-related defect with an absorption line at 3107?cm?1, and ~96% of them were accompanied by a weaker line at 3085.4?cm?1, which is undetectable in most non-milky diamonds. Most of the diamond samples display no platelet defect or a very tiny residual platelet peak with a position at larger wavenumber in milky diamonds than in non-milky counterparts. “Amber center” with a weak but sharp absorption line at 4168.8?cm?1 has been observed in ~73% of the milky diamonds and ~24% of the non-milky ones. Photoluminescence (PL) results reveal that several defects with ZPLs at 490.7, 536, 575.9 and 612.4?nm are more common in milky type IaB diamonds than non-milky ones. A zero-phonon line (ZPL) at 536?nm has been confirmed by PL mapping and CL spectra as a product of plastic deformation, and it might be linked with the H4 center (N4V2 defect). A ZPL at 490.7?nm could be related to a nitrogen-vacancy complex. The defects present more often in milky IaB diamonds are generally associated with plastic deformation. The presence of a hydrogen-related peak at 3085.4?cm?1 and a 536?nm center would help effectively distinguish IaB diamonds with subtle milky areas from their non-milky counterparts.
Diamond & Related Materials, Vol. 89, pp. 322-329.
Russia, India
deposit - Mir, Panna
Abstract: The optical features of milky type IaB diamonds were studied systematically by non-destructive approaches including FTIR, photoluminescence (PL), and cathodoluminescence (CL) spectroscopy. From 97 type IaB diamonds ranging from 0.2?ct to ~100?ct submitted to GIA's New York laboratory for screening, we found that all the milky type IaB diamonds consistently displayed the hydrogen-related defect with an absorption line at 3107?cm?1, and ~96% of them were accompanied by a weaker line at 3085.4?cm?1, which is undetectable in most non-milky diamonds. Most of the diamond samples display no platelet defect or a very tiny residual platelet peak with a position at larger wavenumber in milky diamonds than in non-milky counterparts. “Amber center” with a weak but sharp absorption line at 4168.8?cm?1 has been observed in ~73% of the milky diamonds and ~24% of the non-milky ones. Photoluminescence (PL) results reveal that several defects with ZPLs at 490.7, 536, 575.9 and 612.4?nm are more common in milky type IaB diamonds than non-milky ones. A zero-phonon line (ZPL) at 536?nm has been confirmed by PL mapping and CL spectra as a product of plastic deformation, and it might be linked with the H4 center (N4V2 defect). A ZPL at 490.7?nm could be related to a nitrogen-vacancy complex. The defects present more often in milky IaB diamonds are generally associated with plastic deformation. The presence of a hydrogen-related peak at 3085.4?cm?1 and a 536?nm center would help effectively distinguish IaB diamonds with subtle milky areas from their non-milky counterparts.
European Journal of Mineralogy, doi.org./ 101127/ejm/2018/0030-2783 cost $ 30.00 US
Russia
deposit - Daldyn
Abstract: The spatial distribution patterns of Mg-bearing ilmenite (Ilm) composition were studied on 54 kimberlite bodies of the Daldyn field in the Yakutian kimberlite province. The representativity of the ilmenites sampled in this study is ensured by analysing ca. 100 grains from each kimberlite body. The major conclusions are as follows: (1) ilmenites from neighbouring pipes within the same linear cluster have similar average compositions and compositional fields on the MgO-Cr2O3 plots; (2) ilmenites from different clusters of pipes show different average compositions and compositional fields on the MgO-Cr2O3 plots. (3) regardless of belonging to different clusters, low-Mg Ilm across the whole Daldyn field is characterized by a direct correlation between Al2O3 and MgO; (4) significant changes of MgO content are observed in high-Mg Ilm, while Al2O3 content remains at the same level. The similarity of Ilm compositions across the kimberlite field, as shown by the MgO-Al2O3 plots, is due to a common asthenospheric source. The similar Ilm compositions in different bodies within cluster of pipes is accounted for by a single supply of magma via a lithospheric mantle channel for all pipes of the cluster. The composition of the kimberlite melts can be altered owing to the incorporation and assimilation of lithospheric mantle rocks rich in Mg and Cr. These changes of the melt cause corresponding changes in the Ilm macrocryst composition, both during and after crystallization of Ilm. Thus, the Ilm macrocryst composition follows a trend from low-Mg/low-Cr for Ilm crystallizing in the asthenosphere, to high-Mg/high-Cr at higher levels in the lithosphere. The key conclusion of this study is that Ilm can be used to decipher the structure of kimberlite fields. This can provide a reliable geological criterion for grouping an association of pipes together in clusters, which were previously identified only through subjective considerations of the spatial proximity of kimberlite bodies.
Abstract: The role of fluid(s) in the formation of different lithological facies of kimberlites is still poorly understood. The uncertainty in the composition of kimberlite melts hampers understanding the composition of volatiles, the depth of exsolution, and the effect on magma ascent and fragmentation. Recent estimates of H2O and CO2 solubility in kimberlite-like magmas suggest very shallow exsolution of fluid, while many features of kimberlites indicate the presence of significant fluid fraction at depth. Deep magmatic fluid produces negative trigonal etch pits on natural diamonds, the characteristics of which depend on the temperature and composition of the fluid. Positively oriented trigonal etch pits are very rare on natural diamonds and are likely a feature of resorption events unique to only some kimberlite magmas. Here we present the first systematic study of positively oriented trigonal etch pits on natural diamonds from Snap Lake kimberlite dike, Northwest Territories, Canada. The study used 91 micro-diamonds selected from a population of 251 diamonds representative of all six kimberlite litho-facies identified in the Snap Lake dike. We established that unlike the majority of diamonds from kimberlite pipes in the Northwest Territories, every studied Snap Lake diamond shows positively oriented trigons. These trigons cover the whole diamond surface starting from the {111} faces and continuing over the resorbed edges. They overprint negatively oriented trigons and modify them into hexagons. Atomic force microscopy obtained detailed geometry of 154 positive trigons on 14 diamonds. Three distinct trigon morphologies dependent on the type of the crystal lattice defect were recognized. The point-bottomed shape and positive correlation between the depth and diameter of the individual pits suggest a high CO2 content in the fluid. Comparison with the existing experimental data on positive trigons implies resorption at low-pressure conditions in the 800-1000 °C temperature range by trapped magmatic fluid after the dike emplacement. The intensity of this late resorption event (and the size of the positive trigons) increases from the dike contact with the country rock into the interior of the dike. Such a late resorption event is absent in the majority of kimberlites, which form pipes, and might be a specific feature of hypabyssal kimberlite bodies (dikes). The absence of positive trigons on diamonds from the majority of kimberlites suggests very quick magma cooling below ?800 °C after the pipe emplacement, precluding the development of any late resorption features. Our study shows that for kimberlitic magmas, for which mineral chemistry is unable to provide a robust record of magmatic fluid, morphological details of dissolution features on the surface of diamond and other mantle-derived minerals can serve as a fluid proxy. Better constraints of the pressure, temperature, and oxygen fugacity of the reversal in the trigon orientation on diamond may help to reconstruct the emplacement path of geologically diverse kimberlite bodies.
Abstract: A complex mineral sequence in a kimberlite from the Banankoro Cluster (Guinea Conakry) has been interpreted as the result of magma mixing processes. The composition of the early generations of phlogopite and spinel suggest direct crystallisation of a kimberlitic magma. However, the compositional trends found in the late generations of phlogopite and spinels could suggest magma mixing. In this context, four ilmenite generations formed. The first generations (types 1 and 2) are geikielitic and are associated with spinel and phlogopite which follow the kimberlitic compositional trends. They are interpreted as produced by crystallization from the kimberlite magma. A third generation of euhedral tabular Mg-rich ilmenite (type 3) formed during the interval between two generations of serpentine. Finally, a late generation of Mn-rich ilmenite (type 4) replaces all the Ti-rich minerals and is contemporaneous with the last generation of serpophitic non-replacing serpentine. Therefore, the formation of type 3 and type 4 ilmenite took place after the crystallization of the groundmass, during late hydrothermal process. Our results suggest a detailed textural study is necessary when use Mg-rich and Mn-rich ilmenites as KIMs.
Contributions to Mineralogy and Petrology, Vol. 173, 16p. Doi.org/10.1007/s00410-018-1513-y
Russia
deposit - Udachnaya
Abstract: A xenolith of bimineralic eclogite from the Udachnaya kimberlite pipe provides a snapshot of interaction between mantle rocks and diamond-forming fluids/melts. The major-element composition of the eclogite is similar to that of N-MORB and/or oceanic gabbros, but its trace-element pattern shows the effects of mantle metasomatism, which resulted in diamond formation. The diamonds are clustered in alteration veins that crosscut primary garnet and clinopyroxene. The diamonds contain microinclusions of a fluid/melt dominated by carbonate and KCl. Compared to the worldwide dataset, the microinclusions in these diamonds fall in middle of the range between saline fluids and low-Mg carbonatitic melts. The fluid/melt acted as a metasomatic agent that percolated through ancient eclogitic rocks stored in the mantle. This interaction is consistent with calculated partition coefficients between the rock-forming minerals and diamond-forming fluid/melt, which are similar to experimentally-determined values. Some differences between the calculated and experimental values may be due to the low contents of water and silicates in the chloride-carbonate melt observed in this study, and in particular its high contents of K and LILE. The lack of nitrogen aggregation in the diamonds implies that the diamond-forming metasomatism took place shortly before the eruption of the kimberlite, and that the microinclusions thus represent saline carbonate-rich fluids circulating in the basement of lithospheric mantle (150-170 km depth).
Abstract: The Benfontein kimberlite is a renowned example of a sill complex and provides an excellent opportunity to examine the emplacement and evolution of intrusive kimberlite magmas. We have undertaken a detailed petrographic and melt inclusion study of the Benfontein Upper, Middle and Lower sills. These sills range in thickness from 0.25 to 5?m. New perovskite and baddeleyite U/Pb dating produced ages of 85.7?±?4.4?Ma and 86.5?±?2.6?Ma, respectively, which are consistent with previous age determinations and indicate emplacement coeval with other kimberlites of the Kimberley cluster. The Benfontein sills are characterised by large variations in texture (e.g., layering) and mineral modal abundance between different sill levels and within individual samples. The Lower Sill is characterised by carbonate-rich diapirs, which intrude into oxide-rich layers from underlying carbonate-rich levels. The general paucity of xenogenic mantle material in the Benfontein sills is attributed to its separation from the host magma during flow differentiation during lateral spreading. The low viscosity is likely responsible for non-explosive emplacement of the Benfontein sills, while the rhythmic layering is attributed to multiple magma injections. The Benfontein sills are marked by the excellent preservation of olivine and groundmass mineralogy, which is composed of monticellite, spinel, perovskite, baddeleyite, ilmenite, apatite, calcite, dolomite along with secondary serpentine and glagolevite [NaMg6[Si3AlO10](OH,O)8•H2O]. This is the first time glagolevite is reported in kimberlites. Groundmass spinel exhibits atoll-textures and is composed of a magnesian ulvöspinel magnetite (MUM) or chromite core, surrounded by occasional pleonaste and a rim of Mg-Al-magnetite. We suggest that pleonaste crystallised as a magmatic phase, but was resorbed back into the residual host melt and/or removed by alteration. Analyses of secondary inclusions in olivine and primary inclusions in monticellite, spinel, perovskite, apatite and interstitial calcite are largely composed of Ca-Mg carbonates and, to a lesser extent, alkali-carbonates and other phases. These inclusions probably represent the entrapment of variably differentiated parental kimberlite melts, which became progressively more enriched in carbonate, alkalis, halogens and sulphur during crystal fractionation. Carbonate-rich diapirs from the Lower Sill contain more exotic phase assemblages (e.g., Ba-Fe titanate, barite, ancylite, pyrochlore), which probably result from the extreme differentiation of residual kimberlite melts followed by physical separation and isolation from the parental carbonate-rich magma. It is likely that any alkali or halogen rich minerals crystallising in the groundmass were removed from the groundmass during syn?/post-magmatic alteration, or in the case of Na, remobilised to form secondary glagolevite. The Benfontein sill complex therefore provides a unique example of how the composition of kimberlites may be modified after magma emplacement in the upper crust.
2018 Yellowknife Geoscience Forum , p. 91-92. abstract
Africa, South Africa
deposit - Roberts Victor
Abstract: It is well known that mechanical disaggregation, such as jaw crushing, can cause irreversible damage to valuable gemstones hosted in crystalline rocks. The SELFRAG Lab device uses electrical pulses at high voltages - typically between 150 and 200 kV - to separate material into individual grains along natural boundaries. The purpose of this research is to assess the viability of the SELFRAG as a tool to disaggregate diamond-bearing eclogites, and to assess if this method preserves grains that would otherwise be damaged through mechanical disaggregation. In order to test the applicability of the SELFRAG to diamond recovery from mechanically strong diamond-bearing lithologies, we studied its effects on a diamondiferous eclogite, RV09, from Roberts Victor mine. The Roberts Victor mine is located in South Africa and is renowned for its unusually high abundance of mantle-derived eclogite xenoliths1. Before the eclogite was disaggregated, we bisected the sample and used a CT scan to determine its constituent minerals and the spatial distribution of diamond. One half of the sample was then placed into the SELFRAG, where it was subjected to ~100 shots of 200 kV electrical discharges that segregated the sample into individual grains of similar sizes. The other half was jaw crushed, using a steel jaw crusher which produced non-uniform composite grains and abundant fine material. The varying sizes and aggregate pieces made it difficult to pick diamonds, and after no diamonds were found, the jaw-crushed portion underwent further disaggregation in the SELFRAG. After exerting the same time and effort picking through both portions of the RV09 sample, ten diamonds were recovered from the electronically disaggregated portion, while no diamonds were found in the conventionally disaggregated sample. The diamonds released from the SELFRAG were then imaged with a scanning electron microscope (SEM) to determine the extent to which the diamonds were damaged. Most of the released diamonds showed no evidence of breakage, but a few showed signs of damage that may have occurred prior to kimberlite eruption. The dramatic disparity between the number of diamonds recovered with the SELFRAG and the lack of diamonds in the jaw crushed portion indicates that electrical disaggregation is a superior method compared to the conventional mechanical comminution technique. There are little to no signs of breakage in the SELFRAG-liberated diamonds, whereas, the damage caused by jaw crushing was extensive enough to produce small fragments not readily visible via optical microscopy. The SELFRAG is a promising alternative to conventional disaggregation and offers a practical solution for lessening damage to valuable stones in rocks such as eclogites and kimberlites.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp.319-342.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 253-266.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 425-
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 169-190.
Bulbuc, K.M., Galarneau, M., Stachel, T., Stern, R.A., Kong, J., Chinn, I.
Contrasting growth conditions for sulphide-and garnet-included diamonds from the Victor mine ( Ontario).
2018 Yellowknife Geoscience Forum , p. 97-98. abstract
Canada, Ontario, Attawapiskat
deposit - Victor
Abstract: The Victor Diamond Mine, located in the Attawapiskat kimberlite field (Superior Craton), is known for its exceptional diamond quality. Here we study the chemical environment of formation of Victor diamonds. We imaged eight sulphide-included diamond plates from Victor using cathodoluminescence (CL). Then, along core-rim transects, we measured nitrogen content and aggregation state utilizing Fourier Transform Infrared (FTIR) spectroscopy, and the stable isotope compositions of carbon (?13C) and nitrogen (?15N), using a multi-collector ion microprobe (MC-SIMS). We compare the internal growth features and chemical characteristics of these sulphide inclusion-bearing diamonds with similar data on garnet inclusion-bearing diamonds from Victor (BSc thesis Galarneau). Using this information, possible fractionation processes during diamond precipitation are considered and inferences on the speciation of the diamond forming fluid(s) are explored. Sulphide inclusion-bearing diamonds show much greater overall complexity in their internal growth features than garnet inclusion-bearing diamonds. Two of the sulphide-included samples have cores that represent an older generation of diamond growth. Compared to garnet inclusion-bearing diamonds, the sulphide-included diamonds show very little intra-sample variation in both carbon and nitrogen isotopic composition; the inter-sample variations in carbon isotopic composition, however, are higher than in garnet included diamonds. For sulphide-included diamonds, ?13C ranges from -3.4 to -17.5 and ?15N ranges from -0.2 to -9.2. Garnet inclusion-bearing diamonds showed ?13C values ranging from -4.6 to -6.0 and ?15N ranging from -2.8 to -10.8. The observation of some 13C depleted samples indicates that, unlike the lherzolitic garnet inclusion-bearing diamonds, the sulphide inclusion-bearing diamonds are likely both peridotitic and eclogitic in origin. The total range in N content across sulphide inclusion-bearing diamonds was 2 to 981 at ppm, similar to the garnet-included samples with a range of 5 to 944 at ppm. The very limited variations in carbon and nitrogen isotopic signatures across growth layers indicate that sulphide-included Victor diamonds grew at comparatively high fluid:rock ratios. This is contrasted by the garnet inclusion-bearing diamonds that commonly show the effects of Rayleigh fractionation and hence grew under fluid-limited conditions.
Abstract: The Miaoya carbonatite complex (MCC) is located within the southern edge of the Qinling orogenic belt in central China, and is associated with significant rare earth element (REE) and Nb mineralization. The MCC consists of syenite and carbonatite that were emplaced within Neo- to Mesoproterozoic-aged supracrustal units. The carbonatite intruded the associated syenite as stocks and dikes, and is mainly composed of medium- to fine-grained calcite and abundant REE-bearing minerals. Carbonatite melt generation and emplacement within the MCC occurred during the Silurian (at ~440?Ma), and was subsequently impacted by a late-stage hydrothermal event (~232?Ma) involving REE-rich fluids/melt. This study reports trace element and stable (B, C, and O) and radiogenic (Nd, Pb, and Sr) isotope data for the MCC carbonatite, and these have been subdivided into three groups that represent different REE contents, interpreted as varying degrees of hydrothermal interaction. Overall, the group of carbonatites with the lowest enrichment in LREEs (i.e., least affected by hydrothermal event) is characterized by ?11B values that vary between ?7 (typical asthenospheric mantle) and?+?4‰; ?11B values and B abundances (~0.2 to ~1?ppm) do not correlate with LREE contents. The Sm-Nd and Pb-Pb isotope systems have both been perturbed by the late-stage, REE-rich hydrothermal activity and corroborate open-system behavior. Contrarily, initial 87Sr/86Sr ratios (vary between ~0.70355 and 0.70385) do not correlate significantly with both LREEs and Sr abundances, nor with initial 143Nd/144Nd ratios. The late-stage hydrothermal event overprinted the Nd and Pb isotope compositions for most of the carbonatite samples examined here, whereas a majority of the samples preserve their variable B and Sr isotope values inherited from their mantle source. The B and Sr isotope data for carbonatites exhibiting the least LREE enrichment correlate positively and suggest carbonatite melt generation from a heterogenous upper mantle source that records the input of recycled crustal material. This finding is consistent with those previously reported for young (<300?Ma old) carbonatites worldwide.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 201-222.
Alteration of Mn ilmentite in Horton area of Lena West.
2018 Yellowknife Geoscience Forum , p. 102-103. abstract
Canada, Northwest Territories
deposit - Lena West
Abstract: Mn-ilmenite was recognized as a kimberlite indicator mineral (KIM) in the Lena West diamond region of the Northwest Territories by Darnley Bay, Talmora and Sanatana. It includes compositions that match those found as inclusions in type IIa diamonds from Brazil and Venezuela that formed in the lower mantle. The recent determination that large, high value type IIa diamonds like the Cullinan, Koh-I-Nor, etc. also formed in the lower mantle increases the importance of Mn-ilmenites not only as a KIM resistant to tropical weathering but as a possible indicator of large high value stones. The Mn-ilmenite alteration products, pseudorutile (Fe2Ti3O9) and ferropseudobrookite (FeTi2O5) may also be used as KIMs and provide useful additional information.
Mn-ilmenites found as inclusions in diamonds range from 51 wt.% TiO2 (total wt.% 100) to 56 wt.% TiO2 (total wt.% 95). The shortfall in wt.% of the high TiO2 grains was ascribed by Kaminsky and Belasouva (2009) to some element not included in the analysis. The shortfall may also occur when some ferric iron is calculated as ferrous iron?
As most Lena West Mn-ilmenite analyses have high totals those with totals less than 96 wt.% have been considered an alteration product (“pseudorutile”). “Pseudorutile” is produced by the oxidation of FeO in ilmenite to Fe2O3 which results in an apparent loss of total weight percent when Fe is calculated as ferrous iron. A range of values approximating “ferropseudobrookite” with totals close to 100 wt.% is another alteration product of ilmenite with a loss of iron but without its oxidation to ferric iron.
The Horton area consists of a cluster of magnetic anomalies averaging ~ 200 m diameter east of a very large magnetic anomaly beneath Seahorse Lake. The Seahorse anomaly is at the focus of a train of kimberlite pathfinder elements coincident with a NNW trending KIM train characterised by Mn-ilmenite, picro-ilmenite and chromite. A parallel train of similar KIMs is focused Mn-ilmenite was recognized as a kimberlite indicator mineral (KIM) in the Lena West diamond region of the Northwest Territories by Darnley Bay, Talmora and Sanatana. It includes compositions that match those found as inclusions in type IIa diamonds from Brazil and Venezuela that formed in the lower mantle. The recent determination that large, high value type IIa diamonds like the Cullinan, Koh-I-Nor, etc. also formed in the lower mantle increases the importance of Mn-ilmenites not only as a KIM resistant to tropical weathering but as a possible indicator of large high value stones. The Mn-ilmenite alteration products, pseudorutile (Fe2Ti3O9) and ferropseudobrookite (FeTi2O5) may also be used as KIMs and provide useful additional information. Mn-ilmenites found as inclusions in diamonds range from 51 wt.% TiO2 (total wt.% 100) to 56 wt.% TiO2 (total wt.% 95). The shortfall in wt.% of the high TiO2 grains was ascribed by Kaminsky and Belasouva (2009) to some element not included in the analysis. The shortfall may also occur when some ferric iron is calculated as ferrous iron? As most Lena West Mn-ilmenite analyses have high totals those with totals less than 96 wt.% have been considered an alteration product (“pseudorutile”). “Pseudorutile” is produced by the oxidation of FeO in ilmenite to Fe2O3 which results in an apparent loss of total weight percent when Fe is calculated as ferrous iron. A range of values approximating “ferropseudobrookite” with totals close to 100 wt.% is another alteration product of ilmenite with a loss of iron but without its oxidation to ferric iron. The Horton area consists of a cluster of magnetic anomalies averaging ~ 200 m diameter east of a very large magnetic anomaly beneath Seahorse Lake. The Seahorse anomaly is at the focus of a train of kimberlite pathfinder elements coincident with a NNW trending KIM train characterised by Mn-ilmenite, picro-ilmenite and chromite. A parallel train of similar KIMs is focused on the cluster of smaller anomalies to the east. “Pseudorutile” is found over the cluster of anomalies that lie within the Horton River drainage and in the area north towards Darnley Bay. It was especially abundant with some unaltered Mn-ilmenite grains in the cuttings of a Packsack drill hole that penetrated a few feet of rusty coloured clay coincident with one of the anomalies. It does not appear to travel far. “Ferropseudobrookite” is found mostly west of the Horton River drainage, about 100 kilometers down-ice in the trains coming off the Seahorse anomaly and the cluster of smaller anomalies respectively. It represents the weathering of Mn-ilmenite in the upper part of anomalies that was carried furthest by glaciation indicating a resistance to mechanical wear. Mn-ilmenite is a useful KIM in areas of tropical weathering and is also an indicator of rare large high value diamonds. The distribution of pseudorutile and ferropseudobrookite suggests that the initial alteration of Mn-ilmenite is to pseudorutile and then ferropseudobrookite. The presence of one or the other is therefore a measure of the distance to the source.
Abstract: A detailed electron microprobe study has been carried out on the compositional variations of mica and apatite from carbonatites, phoscorites and associated pyroxenites (and fenites) of the Loolekop deposit, Palabora Carbonatite Complex (South Africa). Mica in pyroxenites and fenites is Mg-rich biotite, whilst micas in carbonatites and phoscorites are compositionally diverse including phlogopite, Ba-rich phlogopite (up to 30% kinoshitalite component), IVAl-rich phlogopite (up to 30% eastonite component) and tetraferriphlogopite. The various types of phlogopites are interpreted as orthomagmatic phases, whereas tetraferriphlogopite precipitation was a late-magmatic to hydrothermal process that additionally introduced REE into the system. Orthomagmatic apatite is generally REE- and Sr-poor fluorapatite and does not show large compositional differences between rock types. Apatite associated with the late-stage tetraferriphlogopite mineralization reaches higher levels of REE (up to 4.9?wt%), Si (up to 1.5?wt% SiO2), Sr (up to 2.6?wt% SrO) and Na (up to 1.0?wt% Na2O). The compositional variation of micas and apatites, which is affiliated with distinct rock types, reflects the multi-stage evolution of the Loolekop deposit and provides detailed insight into the relationships of the carbonatite-phoscorite assemblage. The obtained data support the separation of phoscorite and carbonatite by immiscibility from a common parental magma, which may happen due to a decrease of temperature and/or pressure during the ascent of the magma. This results in a density contrast between the carbonatitic and phoscoritic components that will lead to descending phoscorite accumulations at the outer zones of the magma channel and a jet-like ascent (further promoted by its extremely low viscosity) of the carbonatite magma. The genetic model deduced here explains the peculiar association of carbonatites, phoscorites and silicate rocks in many alkaline complexes worldwide.
The thermochemical conditions of the Diavik lower crust: a kimberlite-hosted xenolith study.
2018 Yellowknife Geoscience Forum , p. 25-26. abstract
Canada, Northwest Territories
deposit - Diavik
Abstract: Thermochemical variables such as lower crustal heat production and Moho temperatures in cratonic regions offer critical insight in constraining the thermal and geodynamic evolution of the lithosphere. In this study, 15 lower crustal granulite xenoliths erupted via the A154N kimberlite at the Diavik mine in the NWT, Canada were studied to quantify the thermal properties of the local Moho and the effects of different heat production models on geotherm models. We quantitatively constrain the thermal properties of the local Moho and the effects of different heat production models on ancient Moho temperatures, the effects of crustal thickness on Moho temperatures, and potential lower crustal compositions. We evaluate the effect of these parameters on total lithospheric thickness estimates. In order to test the accuracy of deep crust thermal calculations, we estimated the ambient temperature of the lower crust at the time of kimberlite eruption through garnet-biotite Fe-Mg exchange geothermometry (Ferry & Spear, 1978). Rim compositions from touching garnet-biotite pairs were used in the calculations and yielded temperatures of 524 ± 77°C (n=20). These represent a maximum estimate of the ambient lower crustal temperature as the closure temperature of garnet-biotite Fe-Mg exchange between garnet and biotite may be higher than the ambient temperature. The primary objective of this study is to quantify lower crustal heat production and its effects on the thermal architecture of cratons. The concentrations of the main heat-producing elements (HPEs) U, Th, and K were quantified via LA-ICP-MS and EPMA in multiple mineral phases per xenolith. By combining these measurements with mineral modes, we derived reconstructed bulk-rock HPE concentrations that were utilized to calculate a range of lower crustal heat production values. This method is preferred over whole-rock analyses as 1) kimberlite is generally enriched in HPEs (Tappe et al. 2013) and can bias trace-element data for their xenoliths and 2) data on individual minerals allows for theoretical lower crustal compositions to be calculated on an idealized basis. A lower crust comprising exclusively mafic granulite (garnet, plagioclase, clinopyroxene ± orthopyroxene) provides a lower bound to heat production (0.07 ± 0.04 W/m3) whereas a lower crust made exclusively of high-grade metasedimentary rocks yields an upper bound (0.42 ± 0.08 W/m3). Both endmembers are present as xenoliths in the A154N kimberlite but mafic granulites predominate following the worldwide trend (Rudnick, 1992). We model the lower crust comprising 20% metasedimentary granulites and 80 % depleted mafic granulites, in accordance with the present xenolith collection. Using this preferred crustal model, we calculate an average heat production of 0.12 ± 0.05 W/m3) for the lower crust beneath Lac de Gras. Utilizing heat flow measurements (Russell et thickness estimates (Mareschal et al. 2004) in conjunction with these HPE determinations, the Moho temperature underlying A-154N can be calculated to be 502 ± 10°C. Using these values along with available mantle xenolith thermobaromtetry (Hasterok & Chapman, 2011) the geotherm is extrapolated to present a mantle potential temperature of 1365°C, at 200 km (FITPLOT, Mather et al, 2011).
Abstract: Over the past year, the Diavik Diamond Mine continued to make significant contributions through its mining operation on Lac de Gras, NWT. The mine is the second largest diamond mine in the NWT (and in Canada), but the largest producer of Canadian rough diamonds. Production has been augmented in 2018 with the official opening and start of mining from a new ore body called A-21.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 343-358.
Abstract: The flux of elements into Earth’s sub-continental lithospheric mantle is facilitated by the passage of small-fraction melts that either crystallise new phases or react with pre-existing minerals. Metasomatised peridotite records the end product of this exchange but rarely captures the process in the act due to subsolidus re-equilibration. We present the results of a systematic investigation of a metasomatic melt channel preserved in a mantle peridotite from the Late Cretaceous Bultfontein kimberlite (Kaapvaal craton) that shows rare direct evidence of the melt-rock reaction processes. We show that the metasomatic proto-kimberlite melt underwent variable crystallisation of clinopyroxene, sulfides, phlogopite, spinel and zircon together with interaction and diffusive exchange with the surrounding olivine-rich mantle. Element profiles across large olivine porphyroclasts (Fo88) show significant core-to-rim variations in Ni (NiO = 0.18-0.32 wt.%) and Cr (Cr = 35-60 ppm), while concentrations of all other elements (e.g. Mg, Fe, Mn, Co, V) are remarkably homogeneous. Electron backscatter diffraction analysis shows that the disequilibrium of Ni and Cr is greatest where the crystal contains large components of the [100] and [010] axes. The disequilibrium is preserved in certain orientations because diffusion of Ni and Cr in olivine is more anisotropic than Fe-Mg and Mn, and slower in the [100] and [010] directions. We present the first observations of Ni and Cr decoupling from other elements in mantle olivine and suggest that this is a consequence of: (i) changing mineral-melt concentration gradients associated with the reactive percolation of a precursory kimberlite melt; and (ii) late-stage sulfide and spinel precipitation. We use the diffusion limited re-equilibration of Ni in olivine to quantify the timing of metasomatism prior to xenolith entrainment by the host kimberlite. Our modelling indicates that reactive percolation occurred on the order of 103-105 years prior to entrainment; this provides an additional line of support for the hypothesis that a period of metasomatism by proto-kimberlite melts precedes the final kimberlite ascent to the surface. The broader implication of our finding of variable rates of minor element diffusion in natural olivine is that it highlights the importance of anisotropy and the impact of changing local concentration gradients during subsolidus re-equilibration.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 119-144.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 223-236.
Canada, Ontario, Attawapiskat, Africa, South Africa
deposit - Victor, Finsch, Newlands
Abstract: Quantitative trace element data from high-purity gem diamonds from the Victor Mine, Ontario, Canada as well as near-gem diamonds from peridotite and eclogite xenoliths from the Finsch and Newlands mines, South Africa, acquired using an off-line laser ablation method show that we see the same spectrum of fluids in both high-purity gem and near-gem diamonds that was previously documented in fibrous diamonds. “Planed” and “ribbed” trace element patterns characterize not only the high-density fluid (HDF) inclusions in fibrous diamonds but also in gem diamonds. Two diamonds from two Finsch harzburgite xenoliths show trace element patterns similar to those of saline fluids, documenting the involvement of saline fluids in the precipitation of gem diamonds, further strengthening the link between the parental fluids of both gem and fibrous diamonds. Differences in trace element characteristics are evident between Victor diamonds containing silicate inclusions compared with Victor diamonds containing sulphide inclusions. The sulphide-bearing diamonds show lower levels of inter-element fractionation and more widely varying siderophile element concentrations - indicating that the silicate and sulphide-bearing diamonds likely formed by gradations of the same processes, via melt-rock reaction or from a subtly different fluid source. The shallow negative LREEN-HREEN slopes displayed by the Victor diamonds establish a signature indicative of original derivation of the diamond forming agent during major melting (~10% melt). Consequently, this signature must have been passed on to HDFs separating from such silicate melts.
Canada, Ontario, Attawapiskat, Africa, South Africa
deposit - Victor, Finsch, Newlands
Abstract: Quantitative trace element data from high-purity gem diamonds from the Victor Mine, Ontario, Canada as well as near-gem diamonds from peridotite and eclogite xenoliths from the Finsch and Newlands mines, South Africa, acquired using an off-line laser ablation method show that we see the same spectrum of fluids in both high-purity gem and near-gem diamonds that was previously documented in fibrous diamonds. “Planed” and “ribbed” trace element patterns characterize not only the high-density fluid (HDF) inclusions in fibrous diamonds but also in gem diamonds. Two diamonds from two Finsch harzburgite xenoliths show trace element patterns similar to those of saline fluids, documenting the involvement of saline fluids in the precipitation of gem diamonds, further strengthening the link between the parental fluids of both gem and fibrous diamonds. Differences in trace element characteristics are evident between Victor diamonds containing silicate inclusions compared with Victor diamonds containing sulphide inclusions. The sulphide-bearing diamonds show lower levels of inter-element fractionation and more widely varying siderophile element concentrations - indicating that the silicate and sulphide-bearing diamonds likely formed by gradations of the same processes, via melt-rock reaction or from a subtly different fluid source. The shallow negative LREEN-HREEN slopes displayed by the Victor diamonds establish a signature indicative of original derivation of the diamond forming agent during major melting (~10% melt). Consequently, this signature must have been passed on to HDFs separating from such silicate melts.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 191-200.
Twenty years at the Ekati diamond mine: corporate social responsibility in action. CSR
2018 Yellowknife Geoscience Forum , p. 47-48. abstract
Canada, Northwest Territories
deposit - Ekati
Abstract: The Ekati Diamond Mine in the Northwest Territories is owned and operated by Dominion Diamond Mines, the largest Canadian independent diamond producer. The Ekati mine was the first diamond mine in Canada, and started production in October 1998. In 2018 the operation is celebrating its twenty year anniversary. In the presentation, we will look back on some of the milestones and achievements of the last two decades. We will also discuss the commitment of the company to make a positive difference in the North through Corporate Social Responsibility initiatives, including support for education, training, community development, business opportunities and respect for the environment. Some examples include:
Community: Whether mining in northern Canada or sorting diamonds in India, we firmly believe that we can - and should - contribute to the social and economic well-being of the communities near our operations. Dominion's Indigenous partners and business operations are important stakeholders and we respect and value their rights, Traditional Knowledge (TK), and cultural heritage.
Hiring, Training and Development: Dominion Diamond Mines is committed to ensuring that the Ekati mine is a welcoming workplace for all employees and that we remain an employer of choice, particularly among northerners and northern Indigenous communities. The company has a number of initiatives and policies to encourage northerners, representatives from Indigenous groups, and women to enter the mining industry. Environment: Throughout the mining process, Dominion Diamond keeps the land and water of the Ekati mine clean and safe for people, plants, and animals. We understand the importance of the Arctic tundra environment and we are committed to mining in the safest, most environmentally responsible way.
Geodynamics and Tectonphysics in RUS, Vol. 9, 3, pp. 827-854. only 1 p. english abstract
Africa, Angola
deposit - Catoca
Abstract: This paper presents the first results of the geostructural and tectonophysical studies of the crustal stress state in the Catoca kimberlite pipe area at the southwestern flank of the Kasai Shield in the northeasternAngola. In the evolution of the crustal stress state, six main stages are distinguished by analyzing the displacements of markers, fold hinges, long axes of boudins, granite dikes of various intrusion phases and kimberlites, as well as fractures with striations. For each of these stages, a dominating horizontal tectonic stress and its orientation is identified. During stage 1 (NW extension and shearing) and at the beginning of stage 2 (NW compression), structures formed in the host rocks in brittle-plastic conditions. The replacement of plastic deformation by faulting could occur about 530-510 Ma ago, when the continental crust ofAfricahad completely formed. Stage 3 (radial, mainly NW extension) and stage 4 (shearing, NW extension, and NE compression) were the most important for kimberlite occurrence: in the Early Cretaceous, radial extension was replaced by shearing. Both stages are related to opening of the central segment of theSouth Atlantic. The main kimberlite magmas occurred during the break-up of the Angola-Brazilian segment of Gondwana. In the course of all the four stages, stress was mainly released by the NE- and E-NE-striking faults and, to a lesser extent, by the NW-striking and latitudinal faults. The initial stage of kimberlite magmatism is associated with the NE- and E-NE-striking faults due to the presence of the Precambrian zones of flow and schistosity, which facilitated the NW-trending subhorizontal extension. Stage 5 (NE compression) began in the second half of the Cretaceous and possibly lasted until the end of the Paleogene, and compression occurred mainly along the NW-striking faults. Regionally, it corresponds to two stages of inversion movements in the southern regions of Africa, during which theAngoladome-shaped uplift emerged and the shoulders of the East African rifts began to take shape. Stage 6 (horizontal extension, mainly in the N-NE direction) is related to the processes that took place in the southern segment of theTanganyikarift and the eastern coast of theAtlantic. Based on the results of our studies, it became for the first time possible to get an idea of the main stages in the evolution of the studied region. Further geostructural measurements and dating of the host rocks will provide for a more precise definition of the proposed stages.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 379-402.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 287-318.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 403-424.
Bridging the gap through care and collaboration: before closure and after production. Snap Lake
2018 Yellowknife Geoscience Forum , pp. 60-61. abstract
Canada, Northwest territories
deposit - Snap Lake
Abstract: Wikipedia defines “Care and Maintenance” as a term used in the mining industry to describe processes and conditions on a closed mine site where there is potential to recommence operations at a later date. During a care and maintenance phase, production is stopped but the site is managed to ensure it remains in a safe and stable condition. De Beers Canada Inc. - Snap Lake Mine entered the Care and Maintenance phase after production ceased in December 2015. The partnership with Det'on Cho Corporation provides for a sustainable execution of care and maintenance activities, taking into consideration approved work plans, mine health and safety considerations and emergency response plans. The mine is currently in its third year of care and maintenance. After exploring the potential sale of the asset and assessing the possibility of reopening the mine, the decision to proceed toward closure was taken in December 2017, ushering Snap Lake into a period of extended care and maintenance (ECM) while a closure plan is developed and finalized. Activities during ECM include monitoring of water quality and other environmental parameters, collecting/treating effluent and making sure that water leaving the site meets water license compliance. Physical infrastructure such as the airstrip, roads, buildings, processed kimberlite containment facilities and associated surface water infrastructure such as sumps, pumps and channels need to be kept in a safe and operable condition. Camp infrastructure such as generators and machinery and equipment are also part of the Care and Maintenance program. Collaboration between the De Beers Canada owner's team and Det'on Cho Corporation resulted in the safe execution of the 2018 work plan which included freshet operations, continued progressive reclamation work, monitoring and maintenance activities. After a trial-run of reduced camp occupancy in the winter of 2017, the site was fully winterized and demobilized in September 2018 to allow for monthly site visits for the duration of the winter and planning for a spring 2019 start-up.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 267-286.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 89-118.
Regier, M.E., Pearson, D.G., Stachel, T., Stern, R.A., Harris, J.
Tracing the formation and abundance of superdeep diamonds.
2018 Yellowknife Geoscience Forum , p. 63. abstract
Africa, Guinea
deposit - Kankan
Abstract: Super-deep diamonds from the transition zone and lower mantle are valuable targets for mining, as they are often large, gem-quality1 or ultra-valuable type IIb stones2. Hence, in mine prospects, it may become important to determine the various populations of sub-lithospheric diamonds. Unambiguously identifying a diamond’s depth of formation is difficult as some minerals can be indicative of various depth regimes (e.g., ferropericlase, Ca-walstromite, enstatite, clinopyroxene, coesite). Here, we use the oxygen isotope compositions of inclusions in Kankan diamonds from Guinea to distinguish between the various diamond-forming processes that happen at lithospheric, asthenospheric to transition zone, and lower mantle depths. In this way, we hope to establish a process by which isotope geochemistry can better constrain the populations of superdeep diamonds in kimberlites, and can assist in estimating a pipe’s propensity for large, valuable stones. Oxygen isotopic analysis by secondary ion mass spectrometry (SIMS) is a high-precision technique that can track hydrothermal alteration that occurred at or close below the ocean floor. Our analyses of inclusions from Kankan diamonds demonstrate that garnets with 3-3.03 Si cations (pfu) have ?18O that are well-constrained within the normal values expected for peridotitic and eclogitic inclusions, but that garnets with ?3.04 Si cations (pfu) have consistently high ?18O (median: 10‰) that slightly decreases with increasing Cr2O3. We interpret this signal as the reaction between a melted carbonate-rich oceanic slab and normal convecting asthenosphere3. In contrast, retrogressed, or former, bridgmanite has ?18O values similar to primitive mantle, suggesting little involvement of slab melts. In contrast to the worldwide suite of lithospheric inclusions of eclogitic paragenesis (median ?18O of 7.03‰)4,5, diamonds derived from ~250 to 500 km have inclusions with consistent, extremely high oxygen isotopes (median: 9.32‰)6,7, due to the melting of extremely enriched carbonated oceanic crust. Diamonds from the lower mantle, however, have inclusions with primitive mantle oxygen isotopes, suggesting a different formation process. The clear distinction in inclusion ?18O between lithospheric, asthenospheric to transition zone, and lower mantle diamond populations is useful in informing the depth regime of a suite of stones, especially those with inclusions of ambiguous depths (e.g., clinopyroxene, coesite, Ca-walstromite, enstatite, ferropericlase, etc.). For instance, we are currently searching for exotic oxygen isotopes in ferropericlase that indicate asthenospheric diamond growth, rather than the primitive mantle values expected for lower mantle ferropericlase. In conclusion, oxygen isotopic analyses of diamond inclusions can identify various sublithsopheric diamond populations, and may benefit the assessment of a mine’s potential for large gem-quality, or type IIb diamonds.
Ramping up from construction to operations: lessons learned at Gahcho Kue diamond mine.
2018 Yellowknife Geoscience Forum , p. 65. abstract
Canada, Northwest Territories
deposit - Gahcho Kue
Abstract: Numerous glacial dispersal trains, spatially and compositionally associated to kimberlites, have been characterized and mapped in the Lac de Gras region, Northwest Territories (NT). However, a small number of these trains have yet to be associated with a source. Additionally, a number of known sub-cropping kimberlites do not have well-defined, spatially associated, trains of indicator minerals. These issues suggest that local factors may be important in controlling the occurrence, shape, and strength of a dispersal pattern and its spatial association with a kimberlite. Identifying these factors and understanding their effect on the dispersion of indicator minerals could provide a road map for finding additional diamondiferous kimberlites in the NT and elsewhere. Here we examine contrasting dispersal trains from south and southwest of Lac de Gras, as well as situations where the source of known dispersal trains (e.g., Coppermine Train) continue to elude exploration geologists. Using both surface and subsurface datasets, we find that the bedrock geology and topography of the source area, as well as those of the dispersal area, are potential key controls on the type and shape of dispersal patterns. Even across discontinuous drift and subdued shield relief we find that bedrock topography and lithology modulated the effect of glacial dynamics on till production and provenance. These 'bedrock factors' have interacted in various ways during Quaternary glaciations, in combinations unique to each case, to generate complex dispersal patterns in three dimensions. Accounting for these factors, using both surface and subsurface data, could enhance the success of drift exploration programs and improve their outcome in the glaciated shield terrains of northern Canada.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 65-88.
Abstract: The ~1100 Ma CC2 and P13 lamproite dykes in the Wajrakarur Kimberlite Field (WKF), Eastern Dharwar Craton, and ~65 Ma Kodomali and Behradih lamproite diatremes in the Mainpur Kimberlite Field (MKF), Bastar Craton share a similar mineralogy, although the proportions of individual mineral phases vary significantly. The lamproites contain phenocrysts, macrocrysts and microcrysts of olivine set in a groundmass dominated by diopside and phlogopite with a subordinate amount of spinel, perovskite, apatite and serpentine along with rare barite. K-richterite occurs as inclusion in olivine phenocrysts in Kodomali, while it is a late groundmass phase in Behradih and CC2. Mineralogically, the studied intrusions are classified as olivine lamproites. Based on microtextures and compositions, three distinct populations of olivine are recognised. The first population comprises Mg-rich olivine macrocrysts (Fo89-93), which are interpreted to be xenocrysts derived from disaggregated mantle peridotites. The second population includes Fe-rich olivine macrocrysts (Fo82-89), which are suggested to be the product of metasomatism of mantle wall-rock by precursor lamproite melts. The third population comprises phenocrysts and overgrowth rims (Fo83-92), which are clearly of magmatic origin. The Mn and Al systematics of Mg-rich olivine xenocrysts indicate an origin from diverse mantle lithologies including garnet peridotite, garnet-spinel peridotite and spinel peridotite beneath the WKF, and mostly from garnet peridotite beneath the MKF. Modelling of temperatures calculated using the Al-in-olivine thermometer for olivine xenocrysts indicates a hotter palaeogeotherm of the SCLM beneath the WKF (between 41 and 43 mW/m2) at ~1100 Ma than beneath the MKF (between 38 and 41 mW/m2) at ~65 Ma. Further, a higher degree of metasomatism of the SCLM by precursor lamproite melts has occurred beneath the WKF compared to the MKF based on the extent of CaTi enrichment in Fe-rich olivine macrocrysts. For different lamproite intrusions within a given volcanic field, lower Fo olivine overgrowth rims are correlated with higher phlogopite plus oxide mineral abundances. A comparison of olivine overgrowth rims from the two fields shows that WKF olivines with lower Fo content than MKF olivines are associated with increased XMg in spinel and phlogopite and vice versa. Melt modelling indicates relatively Fe-rich parental melt for WKF intrusions compared to MKF intrusions. The Ni/Mg and Mn/Fe systematics of magmatic olivines indicate derivation of the lamproite melts from mantle source rocks with a higher proportion of phlogopite and/or lower proportion of orthopyroxene for the WKF on the Eastern Dharwar Craton compared to those for the MKF on the Bastar Craton. This study highlights how olivine cores provide important insights into the composition and thermal state of cratonic mantle lithosphere as sampled by lamproites, including clues to elusive precursor metasomatic events. Variable compositions of olivine rims testify to the complex interplay of parental magma composition and localised crystallisation conditions including oxygen fugacity variations, co-crystallisation of groundmass minerals, and assimilation of entrained material.
Short hold time parameters. Diavik mine water treatment plant.
2018 Yellowknife Geoscience Forum , p. 74-75. abstract
Canada, Northwest Territories
deposit - Diavik
Abstract: It is well known that it is very difficult to transport samples from remote locations to the laboratory and allow sufficient time to commence analysis within the prescribed short hold times for certain parameters. Also, the majority of published hold times are based on legacy as opposed to hard science. In an attempt to determine the validity of specific short hold times, a joint study between Diavik and Maxxam was undertaken. The purpose was to determine the stability of short hold time parameters over time using real samples from Diavik sites. Data from two sites will be presented. The first from the Diavik mine water treatment plant influent, which had relatively high levels of the target analytes. The second from a lake water sample with lower native levels of the target analytes. The parameters studied were ammonia (preserved and unpreserved), total nitrogen, nitrite, nitrate, phosphate, total phosphorus and turbidity. All target parameters have a prescribed 3-day hold time.1 pH was also monitored. Samples were collected by Diavik personnel in one-litre containers and extraordinary logistical measures were taken to get them to Maxxam's Burnaby laboratory as soon as possible. On receipt, they were immediately subsampled into appropriate containers. Each parameter (except pH and turbidity) was split into three containers: 1) as received; 2) low level spike added and 3) medium level spike added. All samples were analyzed within 3 at approximately 3-day intervals thereafter for a period of two weeks.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 359-378.
Siva-Jothy, W., Chinn, I., Stachel, T., Pearson, D.G.
Resorption features of macro and micro diamonds from Gahcho Kue.
2018 Yellowknife Geoscience Forum , p. 120. abstract
Canada, Northwest Territories
deposit - Gahcho Kue
Abstract: Studies into the relationship between oxygen fugacity of mantle fluids/melts and etch features on diamond surfaces have shown specific fluid/melt compositions correspond to associated etch features. A classification scheme has been proposed to determine the fluid composition within a kimberlite by examining etch features associated with diamond surfaces as a proxy for fluid composition in an ascending diamondiferous kimberlite. A suite of 388 microdiamonds (defined as diamonds which pass through a 0.5 mm square mesh screen) and 88 macrodiamonds taken from various drill hole depths in the Hearne kimberlite and 88 inclusion-bearing macrodiamonds from the Gahcho Kué mine (NWT) were viewed under a secondary electron microscope for their surface features in accordance with this scheme. Two hundred and thirty specimens show shallow-depth etch features that can be easily classified: the main features observed were trigons and truncated trigons on the {111} faces and/or tetragons on the {100} faces (indicating etching by fluids of variable CO2:H2O ratios). Thirty-four specimens show deeper etched features that represent either extreme degrees of regular etching (such as deeply-etched tetragons), or corrosion type etching, wherein the diamond lattice is etched in a fluid-free melt. Variability between crystal habits exists between the size fractions studied, with cubic habits only being observed in the microdiamond population. This implies variable formation conditions for the two different diamond size fractions studied from Gahcho Kué. Among microdiamonds, surface textures associated with fluid-related etching are markedly more variable, with truncated trigons, tetragons, and both positive and negative trigons being observed. However, these often occur in combination with features showing a large variability in their depth to size ratio between samples, which is typically caused by mantle-related etching. These observations suggest repeated interaction of fluids/melts with the Gahcho Kué diamond population, with at least some of the fluids affecting the microdiamonds being more CO2-rich than those that etched the macrodiamond fraction.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 49-64.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 237-252.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 145-168.
Stirling, R.A., Kelley, S.E., Ross, M., Elliott, B., Normandeau, P.X.
Surface and subsurface till characteristics in a drumlin field south of Lac de Gras, NT; implications for drift prospecting. ( Dominion's Ekati and North Arrow)
2018 Yellowknife Geoscience Forum , p. 80. abstract
Canada, Northwest Territories
deposit - Ekati
Abstract: Successful diamond exploration is becoming increasingly challenging as the best expressed targets have been found. Areas of variable drift thickness and heterogeneous surficial deposits present several challenges to exploration. One particular aspect that is poorly understood is the effect of well-developed drumlin fields on the surface expression of dispersal trains. Our study focuses on drumlin fields and their potential effects in the expression of a dispersal pattern. Because drumlins are often stratified we hypothesize that multiple till layers of contrasting provenance, representing multiple ice-flow directions, can occur at the surface across drumlin fields due to erosional processes. This has the potential to affect analysis and interpretation of surficial till dispersion data.
To test this hypothesis, we examined data from a large RC drilling dataset donated by Dominion Diamond Ekati Corp. and North Arrow Minerals Inc. and complemented it with field-based surficial geology observations and analysis of additional surficial till samples across targeted drumlins. The surficial samples were collected at the top and on the sides of drumlins to test whether any glacial stratigraphy is expressed, especially in areas where post-glacial erosion may have exposed internal drumlin stratigraphy. Based on the RC data and available maps drift thickness within the drumlin field ranges from 1 meter in the swales between drumlins to about 20 meters on the top of the highest amplitude drumlins. Locally measured ice-flow indicators (n=11) show three distinct ice-flow directions from older to youngest: 260, 290, 305 degrees. Preliminary analysis of textural and compositional data shows variations within the till at depth as well as across the drumlin field. Ongoing work focuses on determining the relationship (or lack thereof) between till characteristics, drumlins, and ice flow history (till provenance), as well as on three-dimensional dispersal patterns of kimberlite indicator minerals and related geochemical pathfinders. This work will highlight landform feature considerations by using multiple parameters to analyze sample data in areas with complex glacial geology and high diamond potential.
Abstract: A study of the morphology, mineral inclusions, nitrogen content, and nitrogen aggregation state of diamonds from the Voorspoed kimberlite, was conducted. The diamonds are characterised by a highly unusual inclusion mineral paragenesis dominated by eclogitic and transitional websteritic-lherzolitic inclusions along with related websteritic inclusions, while a comparatively minor harzburgitic diamond inclusion suite account for the remainder. This differs substantially from many of the diamond populations in kimberlites on the Kaapvaal Craton where a harzburgitic inclusion paragenesis predominates. Only in the case of the Orapa kimberlite in Botswana has a similar diamond inclusion suite been encountered before, although in that instance an eclogitic and websteritic inclusion suite predominate. Calculated garnet-clinopyroxene equilibration temperatures, at an assumed pressure of 50?kbar, range from 1040 °C to 1296?°C. Temperatures of 1114?°C to 1348?°C, at 50?kbar, are calculated for lamellar orthopyroxene-clinopyroxene intergrowths. ‘Reconstituted’ pyroxenes mathematically reconstructed from the lamellar orthopyroxene-clinopyroxene intergrowths produce temperatures of 1238?°C to 1416?°C, suggesting that the lithosphere cooled by at least 100?°C after diamond crystallisation. Nitrogen contents and nitrogen aggregation states of whole diamonds range from below the detection limit (~10?ppm) to 1442 atomic ppm (average 167 atomic ppm), and up to 97% of the highly aggregated ‘B' component (average 65%), respectively. The elevated aggregation state of the nitrogen in the diamonds from Voorspoed, coupled with a high level of platelet degradation in many of the diamonds analysed, relative to a world-wide database, is unusual, but broadly comparable to diamonds from kimberlites occurring in craton margin settings, such as Argyle and Venetia. Diamond inclusion thermobarometry, as well as the elevated nitrogen aggregation states of the diamonds (coupled with the evidence for platelet degradation in the diamonds) are indicative of a diamond crystallisation event associated with a transient thermal pulse, as well as associated deformation of the mantle containing the diamonds. The websteritic and the transitional websteritic-lherzolitic mantle source rocks of the Voorspoed diamonds likely formed through melt infiltration into mantle peridotite, possibly in the reaction envelope surrounding an ascending mantle plume. In order to account for the unusually low abundance of harzburgitic diamonds at Voorspoed, it is postulated that a primary, pre-existing suite of harzburgitic diamonds which have crystallised in the Mesoarchaean, was destroyed through heating and oxidation during the passage of magmas associated with the Ventersdorp large igneous province at 2.72?Ga, and which was subsequently followed by the crystallisation of a younger eclogitic and transitional websteritic-lherzolitic suite of diamonds.
Till geochemistry and lithogeochemical exploration for a concealed kimberlite.
2018 Yellowknife Geoscience Forum , p. 88-89. abstract
Canada, Northwest Territories
deposit - Kelvin
Abstract: Research at the Kelvin kimberlite, NWT is defining surface exploration practices and developing new exploration tools based on host rock lithogeochemical alteration, that will result in reduced costs and improved discovery success. In regions where recent glaciation has buried kimberlites under glacial sediments, surface geochemical detection methods are best interpreted when coupled with a comprehension of the landscape formation processes. The glacial, post-glacial, and cryoturbation processes that have affected the landscape have, in turn, affected the dispersal of geochemical signatures in the till that can be detected and exploited by detailed surface mapping, sampling, and geochemical analysis. Additionally, the application of geochemical and hyperspectral data to country rock alteration core can aid in the detection of kimberlites during near-miss drilling campaigns. The Kelvin kimberlite is located eight kilometers from the Gahcho Kué diamond mine in the Northwest Territories. The inclined pipe sub-crops beneath a lake and dips into gneiss country rock towards the northwest with a surface projection of more than 600 m long. Relative uniformity of surficial material (<6 m thick till veneer) allows for extensive b-horizon soil sampling above the kimberlite, up-ice, and up to 1 km in the down-ice direction. Samples were sieved to -180 microns and analyzed by four acid digest ICP-MS and aqua-regia digest ICP-MS. Results indicate the soils to be very immature and identify the presence of a subtle Ni-Cr-Mg-Nb train originating from the lake side extending for >1km from source following the most recent ice direction to the west. The material for the train was abraded by the ice from the kimberlite, now sub-cropping beneath a lake, and would have provided additional support to drill what was initially targeted from geophysics. Additional research is being carried out to detect alteration signatures in the country rock induced by the emplacement of the kimberlite. Lithogeochemical data from four drill holes aims to identify and quantify the metasomatic enrichment and depletion of elements sourced from the kimberlite while accounting for country-rock lithology variation. Hyperspectral imaging of the same drill core will aim to detect and quantify secondary mineralogy and subtle changes in mineral composition that otherwise cannot be detected visually. This data will be used to generate mineralogical and chemical vectors beneficial in near-miss situations when drilling kimberlites and defining diatreme geometries.
Abstract: Diamonds from Juina, Brazil, are well-known examples of superdeep diamond crystals formed under sublithospheric conditions and evidence would indicate their origins lie as deep as the Earth’s mantle transition zone and the Lower Mantle. Detailed characterization of these minerals and of inclusions trapped within them may thus provide precious minero-petrogenetic information on their growth history in these inaccessible environments. With the aim of studying non-destructively the structural defects in the entire crystalline volume, two diamond samples from this locality, labelled JUc4 and BZ270, respectively, were studied in transmission mode by means of X-ray Diffraction Topography (XRDT) and micro Fourier Transform InfraRed Spectroscopy (µFTIR). The combined use of these methods shows a good fit between the mapping of spatial distribution of extended defects observed on the topographic images and the µFTIR maps corresponding to the concentration of N and H point defects. The results obtained show that both samples are affected by plastic deformation. In particular, BZ270 shows a lower content of nitrogen and higher deformation, and actually consists of different, slightly misoriented grains that contain sub-grains with a rounded-elongated shape. These features are commonly associated with deformation processes by solid-state diffusion creep under high pressure and high temperature.
Gems & Gemology, Sixth International Gemological Symposium Vol. 54, 3, 1p. Abstract p. 273-4.
Africa, Botswana
deposit - Karowe
Abstract: In November 2015, Lucara Diamond’s operation at the Karowe mine in Botswana gained notoriety due to the extraction of a series of large colorless diamonds, including the 1,109 ct Lesedi La Rona and the 812 ct Constellation. The Lesedi La Rona marks the largest gem diamond recovered since the Cullinan (3,106 ct) in 1905. The Constellation, considered to be the seventh-largest recorded diamond, attained the highest price ever paid for a rough, selling for $63.1 million ($77,649 per carat). Additionally, three other significant colorless diamonds were recovered during the same period, weighing 374, 296, and 183 ct. Due to the similarity in their external characteristics— which include cleavage faces—as well as their extraction locations and dates, it was suspected that these stones might have originated from a larger rough that had broken. Lucara demonstrated that the 374 ct diamond and the Lesedi La Rona fit together, yet a large cleavage plane is still unaccounted for. GIA was able to study several rough and/or faceted pieces of these five diamonds using a range of spectroscopic and imaging techniques to gain insight into the presence and distribution of point defects in these diamonds. Diamonds are commonly classified according to their nitrogen content measured by Fourier-transform infrared (FTIR) spectroscopy: Type I diamonds contain nitrogen in either isolated (Ib) or aggregated (IaAB) forms, while type II diamonds do not contain detectable nitrogen concentrations (IIa) but may contain boron (IIb). Analysis of faceted stones cut from the Lesedi La Rona indicates that the rough is a mixed-type diamond, containing both type IIa and pure type IaB regions. These types of diamonds, though exceedingly unusual, have been observed at GIA and reported by Delaunay and Fritsch (2017). The Constellation and the 374, 296, and 183 ct diamonds were determined to be type IaB, containing 20 ± 4 ppm B-aggregates (N4V), in agreement with the concentration for the type IaB pieces of the Lesedi La Rona. Pure type IaB diamonds such as these are actually quite rare, accounting for only 1.2% of a random suite of 5,060 large (>10 ct) D-to-Z diamonds submitted to GIA, whereas 24.6% were type II. Photoluminescence spectra further confirmed analogous defect content for the five large Karowe diamonds, with emissions from H4 (N4V2 0, 496 nm), H3 (NVN0, 503 nm), 505 nm, NV– (637 nm), and GR1 (V0, 741 nm) defects showing similar relative intensities and peak widths. Even for diamonds of the same type, parallel defect content and characteristics across such a variety of defects is unlikely for unrelated stones. The external morphologies of the diamonds showed primary octahedral, resorbed, and fractured faces, with the Constellation and the 296 ct diamond featuring fractures containing metallic inclusions and secondary iron oxide staining. Deep UV fluorescence (< 230 nm) imaging elucidated the internal growth structures of the samples. For the Constellation and the 374, 296, and 183 ct diamonds, at least two growth zones with differing blue fluorescence intensities were observed within single pieces. Combined with the spectroscopic data, these results provide compelling evidence that the Lesedi La Rona, the Constellation, and the 374, 296, and 183 ct diamonds from Karowe had comparable growth histories and likely originated from the same rough, with a combined weight of at least 2,774 ct.
Abstract: Carbonate-rich intrusions in contact with felsic rocks theoretically should show the effects of interaction between the two rock types, due to their contrasting compositions. In reality, though, such interaction is rarely reported at kimberlite contacts. We present the first documented case of lithological and mineralogical zonation at the margin of a kimberlite, the Snap Lake dyke, in contact with the wall-rock granitoid. Our detailed petrographic, mineralogical and geochemical study shows that the fresh hypabyssal kimberlite consists of olivine macrocrysts and microcrysts, and phlogopite macrocrysts set in a groundmass of serpentinized monticellite, phlogopite, spinel, perovskite and apatite, with interstitial lizardite and calcite. This typical Group I kimberlite mineralogy does not match the bulk-rock composition, which resembles a Group II micaceous kimberlite. The mismatch between the chemical and mineralogical properties is ascribed to contamination by granitoid xenoliths and metasomatic reactions with the felsic country rocks, the Snap Lake kimberlite has extremely low bulk-Ca compared to other documented Group I kimberlites. Reaction with deuteric H2O and CO2 has led to Ca removal, serpentinization of olivine, replacement of calcite by dolomite, alteration of perovskite and decomposition of apatite. Adjacent to the contact with the host granitoid and in haloes around granitoid clasts, poikilitic phlogopite and lizardite are replaced by subsolidus phlogopite and a multiphase phyllosilicate composed of phlogopite+?lizardite+?chlorite+?talc. A modified isocon analysis accounts for felsic xenolith assimilation and isolates metasomatic changes. Enrichment of altered kimberlites in Si owes solely to xenolith incorporation. The metasomatic ingress of granitoid-derived Al for a limited distance inside the dyke was counteracted by a flux of Mg and Fe to the granitoid. Metasomatic changes in K and Ca tend to be positive in all lithologies of kimberlite and in the granitoids implying distal transport. The combination of xenolith digestion with metasomatic element transport is expected in hybrid zones where kimberlite magmas interact with felsic wall-rocks.
European Journal of Mineralogy, Vol. 30, 6, pp. 1083-1094.
Russia, Yakutia
deposit - Dalydyn
Abstract: The spatial distribution patterns of Mg-bearing ilmenite (Ilm) composition were studied on 54 kimberlite bodies of the Daldyn field in the Yakutian kimberlite province. The representativity of the ilmenites sampled in this study is ensured by analysing ca. 100 grains from each kimberlite body. The major conclusions are as follows: (1) ilmenites from neighbouring pipes within the same linear cluster have similar average compositions and compositional fields on the MgO-Cr2O3 plots; (2) ilmenites from different clusters of pipes show different average compositions and compositional fields on the MgO-Cr2O3 plots. (3) regardless of belonging to different clusters, low-Mg Ilm across the whole Daldyn field is characterized by a direct correlation between Al2O3 and MgO; (4) significant changes of MgO content are observed in high-Mg Ilm, while Al2O3 content remains at the same level. The similarity of Ilm compositions across the kimberlite field, as shown by the MgO-Al2O3 plots, is due to a common asthenospheric source. The similar Ilm compositions in different bodies within cluster of pipes is accounted for by a single supply of magma via a lithospheric mantle channel for all pipes of the cluster. The composition of the kimberlite melts can be altered owing to the incorporation and assimilation of lithospheric mantle rocks rich in Mg and Cr. These changes of the melt cause corresponding changes in the Ilm macrocryst composition, both during and after crystallization of Ilm. Thus, the Ilm macrocryst composition follows a trend from low-Mg/low-Cr for Ilm crystallizing in the asthenosphere, to high-Mg/high-Cr at higher levels in the lithosphere. The key conclusion of this study is that Ilm can be used to decipher the structure of kimberlite fields. This can provide a reliable geological criterion for grouping an association of pipes together in clusters, which were previously identified only through subjective considerations of the spatial proximity of kimberlite bodies.
Contributions to Mineralogy and Petrology, Vol. 173, 12, pp. 106-
Russia, Kola Peninsula
deposit - Afrikanda
Abstract: Perovskite is a common accessory mineral in a variety of mafic and ultramafic rocks, but perovskite deposits are rare and studies of perovskite ore deposits are correspondingly scarce. Perovskite is a key rock-forming mineral and reaches exceptionally high concentrations in olivinites, diverse clinopyroxenites and silicocarbonatites in the Afrikanda alkaline-ultramafic complex (Kola Peninsula, NW Russia). Across these lithologies, we classify perovskite into three types (T1-T3) based on crystal morphology, inclusion abundance, composition, and zonation. Perovskite in olivinites and some clinopyroxenites is represented by fine-grained, equigranular, monomineralic clusters and networks (T1). In contrast, perovskite in other clinopyroxenites and some silicocarbonatites has fine- to coarse-grained interlocked (T2) and massive (T3) textures. Electron backscatter diffraction reveals that some T1 and T2 perovskite grains in the olivinites and clinopyroxenites are composed of multiple subgrains and may represent stages of crystal rotation, coalescence and amalgamation. We propose that in the olivinites and clinopyroxenites, these processes result in the transformation of clusters and networks of fine-grained perovskite crystals (T1) to mosaics of more coarse-grained (T2) and massive perovskite (T3). This interpretation suggests that sub-solidus processes can lead to the development of coarse-grained and massive perovskite. A combination of characteristic features identified in the Afrikanda perovskite (equigranular crystal mosaics, interlocked irregular-shaped grains, and massive zones) is observed in other oxide ore deposits, particularly in layered intrusions of chromitites and intrusion-hosted magnetite deposits and suggests that the same amalgamation processes may be responsible for some of the coarse-grained and massive textures observed in oxide deposits worldwide.
Abstract: The ~1100?Ma CC2 and P13 lamproite dykes in the Wajrakarur Kimberlite Field (WKF), Eastern Dharwar Craton, and ~65?Ma Kodomali and Behradih lamproite diatremes in the Mainpur Kimberlite Field (MKF), Bastar Craton share a similar mineralogy, although the proportions of individual mineral phases vary significantly. The lamproites contain phenocrysts, macrocrysts and microcrysts of olivine set in a groundmass dominated by diopside and phlogopite with a subordinate amount of spinel, perovskite, apatite and serpentine along with rare barite. K-richterite occurs as inclusion in olivine phenocrysts in Kodomali, while it is a late groundmass phase in Behradih and CC2. Mineralogically, the studied intrusions are classified as olivine lamproites. Based on microtextures and compositions, three distinct populations of olivine are recognised. The first population comprises Mg-rich olivine macrocrysts (Fo89-93), which are interpreted to be xenocrysts derived from disaggregated mantle peridotites. The second population includes Fe-rich olivine macrocrysts (Fo82-89), which are suggested to be the product of metasomatism of mantle wall-rock by precursor lamproite melts. The third population comprises phenocrysts and overgrowth rims (Fo83-92), which are clearly of magmatic origin. The Mn and Al systematics of Mg-rich olivine xenocrysts indicate an origin from diverse mantle lithologies including garnet peridotite, garnet-spinel peridotite and spinel peridotite beneath the WKF, and mostly from garnet peridotite beneath the MKF. Modelling of temperatures calculated using the Al-in-olivine thermometer for olivine xenocrysts indicates a hotter palaeogeotherm of the SCLM beneath the WKF (between 41 and 43?mW/m2) at ~1100?Ma than beneath the MKF (between 38 and 41?mW/m2) at ~65?Ma. Further, a higher degree of metasomatism of the SCLM by precursor lamproite melts has occurred beneath the WKF compared to the MKF based on the extent of CaTi enrichment in Fe-rich olivine macrocrysts. For different lamproite intrusions within a given volcanic field, lower Fo olivine overgrowth rims are correlated with higher phlogopite plus oxide mineral abundances. A comparison of olivine overgrowth rims from the two fields shows that WKF olivines with lower Fo content than MKF olivines are associated with increased XMg in spinel and phlogopite and vice versa. Melt modelling indicates relatively Fe-rich parental melt for WKF intrusions compared to MKF intrusions. The Ni/Mg and Mn/Fe systematics of magmatic olivines indicate derivation of the lamproite melts from mantle source rocks with a higher proportion of phlogopite and/or lower proportion of orthopyroxene for the WKF on the Eastern Dharwar Craton compared to those for the MKF on the Bastar Craton. This study highlights how olivine cores provide important insights into the composition and thermal state of cratonic mantle lithosphere as sampled by lamproites, including clues to elusive precursor metasomatic events. Variable compositions of olivine rims testify to the complex interplay of parental magma composition and localised crystallisation conditions including oxygen fugacity variations, co-crystallisation of groundmass minerals, and assimilation of entrained material.
Abstract: Apatite can host significant levels of trace elements, including REE, within its crystal lattice, making it particularly useful for deciphering geological events and processes. This study employs hyperspectral cathodoluminescence (CL) and in situ microchemical techniques to identify and characterize various generations of apatite occurring in the phoscorites, carbonatites, and fenites of the Gifford Creek Carbonatite Complex (GCCC), Western Australia. Hyperspectral CL revealed that apatite crystals in all samples have complex internal zoning, including multiple distinct generations, with zones of relatively bright CL generally having more complex spectra compared to darker CL zones. Most of the CL spectra have prominent sharp peaks at ?1.4 eV and ?2.l eV as well as a broad peak between 2.3 eV and 3.5 eV. We relate these different peaks to individual REE activators and groups of activators, in particular Nd3+, Eu3+, Sm3+, and Ce3+. Trace element analyses of apatite confirm the relative enrichment of REE in the CL brighter zones. Most apatite generations exhibit concave-down to sinusoidal REY patterns lacking Eu anomalies, but often feature distinct negative Y anomalies. The depletion in LREE is interpreted to be due to LREE sequestration into monazite, which is relatively abundant in most of the samples. Most apatite samples contain very low Si contents, but appreciable Na, so REE incorporation into apatite was primarily via a coupled substitution of REE + Na replacing 2Ca, which is consistent with the highly alkaline, low SiO2 environment under which the apatite formed. Based on the combined trace-element signatures and CL textures, we interpret the multiple generations of apatite to reflect magmatic growth from alkaline magmas followed by recrystallization during subsequent metamorphic/hydrothermal events. The notable exception is the apatite core domains from a fenite sample that contain relatively high Si and Mn contents, low Sr, and relatively HREE-enriched REY patterns with distinct negative Eu anomalies. This apatite is interpreted to be relict from the granitic precursor to fenitization. The apatite samples also show systematic compositional variations across the GCCC, with apatite from phoscorite samples from the southeast part of the complex containing higher Sr, lower Gd/Ce, and lower ?3 values (normalized REE pattern inflections) compared to apatite from the northwest part of the complex. Recognition of these spatial variations in apatite compositions from the intra-grain micro-scale through to the district scale demonstrates the utility of combining advanced petrographic methods, such as hyperspectral CL, with micro-chemical analysis to reveal complex geological records preserved in apatite. As apatite is a common accessory mineral, these techniques may be more broadly applicable to igneous source tracing, understanding metamorphic and/or metasomatic processes, provenance studies from detrital mineral records, and studies of the evolution of ore systems.
Gems & Gemology, Sixth International Gemological Symposium Vol. 54, 3, 1p. Abstract p. 307.
Africa, Sierra Leone
deposit - zimmi
Abstract: Type Ib diamonds from Zimmi, Sierra Leone, have 500 My mantle residency times whose origin is best explained by rapid tectonic exhumation after continental collision to shallower depths in the mantle prior to kimberlite eruption (Smit et al., 2016). Here we present spectroscopic data for a new suite of Zimmi sulfide-bearing type Ib diamonds that allow us to evaluate the link between their rare Fancy yellow colors, the distribution of their spectroscopic features, and their unusual geological history. Cathodoluminesence (CL) imaging revealed irregular patterns with abundant deformation lamellae, associated with the diamonds’ tectonic exhumation (Smit et al., 2018). Vacancies formed during deformation were subsequently naturally annealed to form vacancy clusters, NV0/? centers, and H3 (NVN0). The brownish yellow to greenish yellow colors observed in Zimmi type Ib diamonds result from visible absorption by a combination of isolated nitrogen and deformation-related vacancy clusters (Smit et al., 2018). Color-forming centers and other spectroscopic features can all be attributed to the unique geological history of Zimmi type Ib diamonds and their rapid exhumation after formation.
Gems & Gemology, Sixth International Gemological Symposium Vol. 54, 3, 1p. Abstract p. 274.
Africa, South Africa, Angola
deposit - Cullinan, Lulo
Abstract: Many of the world’s largest and most valuable gem diamonds exhibit an unusual set of physical characteristics. For example, in addition to their conspicuously low nitrogen concentrations, diamonds such as the 3,106 ct Cullinan (type IIa) and the Hope (type IIb, boron bearing) tend to have very few or no inclusions, and in their rough state they are found as irregular shapes rather than as sharp octahedral crystals. It has long been suspected that type IIa and IIb diamonds form in a different way than most other diamonds. Over the past two years, systematic investigation of both type IIa and IIb diamonds at GIA has revealed that they sometimes contain rare inclusions from unique geological origins. Examination of more than 130 inclusion-bearing samples has established recurring sets of inclusions that clearly show many of these diamonds originate in the sublithospheric mantle, much deeper in the earth than more common diamonds from the cratonic lithosphere. We now recognize that type IIa diamonds, or more specifically, diamonds with characteristics akin to the historic Cullinan diamond (dubbed CLIPPIR diamonds), are distinguished by the occurrence of ironrich metallic inclusions. Less frequently, CLIPPIR diamonds also contain inclusions of majoritic garnet and former CaSiO3perovskite that constrain the depth of formation to within 360–750 km. The inclusions suggest that CLIPPIR diamonds belong to a unique paragenesis with an intimate link to metallic iron in the deep mantle (Smith et al., 2016, 2017). Similarly, findings from type IIb diamonds also place them in a “superdeep” sublithospheric mantle setting, with inclusions of former CaSiO3 perovskite and other high-pressure minerals, although the iron-rich metallic inclusions are generally absent (Smith et al., 2018). Altogether, these findings show that high-quality type II gem diamonds are predominantly sourced from the sublithospheric mantle, a surprising result that has refuted the notion that all superdeep diamonds are small and nongem quality. Valuable information about the composition and behavior of the deep mantle is cryptically recorded in these diamonds. CLIPPIR diamonds (figure 1) confirm that the deep mantle contains metallic iron, while type IIb diamonds suggest that boron and perhaps water can be carried from the earth’s surface down into the lower mantle by plate tectonic processes. In addition to being gemstones of great beauty, diamonds carry tremendous scientific value in their unique ability to convey information about the interior of our planet.
Gems & Gemology, Sixth International Gemological Symposium Vol. 54, 3, Fall 1p. Abstract p. 262-3
Africa, Sierra Leone
deposit - Zimmi
Abstract: Isolated nitrogen is one of the major defects in producing yellow color in natural diamonds. In regular type Ib yellow diamonds, isolated nitrogen is normally the dominant form, with limited aggregations in A centers (nitrogen pairs). Type Ib diamonds normally experienced strong plastic deformations. In addition to vacancy clusters, many other optic centers were introduced during annealing over their long geological history, such as GR1, NV, and H3 centers. Diamonds from the Zimmi area of West Africa are a typical example (Smit et al., 2016). As a result, clear brownish and greenish hues are common among these diamonds, so most do not possess true “canary” yellow color. Here we studied more than 2,000 diamonds with real canary yellow color. Their color origin and relationship with type Ib diamonds were explored. Sizes of the studied diamonds ranged from 0.01 to about 1.0 ct. They showed pure yellow color, with grades of Fancy Intense or Fancy Vivid yellow. Infrared absorption analysis showed that they were all type IaA with very high nitrogen concentrations, but a very weak absorption from isolated nitrogen at 1344 cm–1 was detected in all samples. Concentration of isolated nitrogen was estimated at ~2–3 ppm. This isolated nitrogen created smooth absorption in the ultraviolet-visible (UV-Vis) region, increasing gradually to the high-energy side. No other defects were detected using UV-Vis absorption spectroscopy, which explained the pure yellow color we observed. Fluorescence imaging revealed multiple nucleation centers with dominant green color, which was attributed to the S3 defects confirmed through photoluminescence analysis. Compared with natural type Ib diamonds, an outstanding feature of the studied samples is the absence of plastic deformation. For this reason, other vacancy-related defects were not introduced to these diamond lattices over the geological period after their formation. Sulfide inclusions are common in type Ib diamonds, but they were not observed in these canary stones. Instead, some calcite inclusions were observed. All the observations from this study indicated that the canary diamond samples were formed in a different geological environment than type Ib diamonds.
Abstract: The late Mesoproterozoic Ngualla carbonatite complex in southwest Tanzania comprises a central magnesiocarbonatite plug surrounded sequentially by an annular calcite carbonatite intrusion and fenitised felsic igneous country rocks. The calcite carbonatite contains phlogopite-rich (glimmerite) enclaves interpreted as fenitised wallrock xenoliths that have contributed silicate minerals, apatite and magnetite through dispersal and interaction, mainly within the calcite carbonatite magma. Ultramafic magmas were emplaced into the magnesiocarbonatite magma chamber before complete solidification of the magnesiocarbonatite. Contemporaneity allowed the two magmas to mingle. Rounded enclaves of hematite-barite in the magnesiocarbonatite are tentatively attributed to magma immiscibility. Following complete solidification of the calcite carbonatite, and overlapping late crystallization of the magnesiocarbonatite plug, late magnesiocarbonatite dikes and ultramafic dikes were emplaced, some of the latter as diatremes. Crystallization of ferroan dolomite in the magnesiocarbonatite plug resulted in residual magmatic concentration of Si, Ba, F and rare earth elements (REE), and crystallization of barite, quartz, calcite, fluorite and REE fluorocarbonates in miarolitic cavities. Concentrations of (total) rare earth oxides (TREO) in the unweathered magnesiocarbonatite are 1 to 2%. REE ore with 3 to 6% TREO resulted from weathering, during which CaCO3 and MgCO3 were leached from ferroan dolomite leaving a porous goethite-rich residue containing barite and bastnaesite, the latter having replaced primary synchesite. Other commodities with potential economic significance include phosphate and niobium, both of which were enriched by residual accumulation over the calcite carbonatite as a result of karstic weathering. Although weathering was a critical factor in the formation of REE ore at Ngualla, the primary proto-ore resulted mainly from in situ igneous processes. This genetic model is different from that used to account for many carbonatite-hosted ore bodies, which result from late-stage hydrothermal processes. Examples of hydrothermal rare earth deposits include those of the late Jurassic to early Cretaceous Chilwa Province, located 800?km south of Ngualla. The differences in ore-forming processes may reflect the relative ages of the carbonatites and a deeper level of erosion at Ngualla.
Abstract: The Benfontein kimberlite is a renowned example of a sill complex and provides an excellent opportunity to examine the emplacement and evolution of intrusive kimberlite magmas. We have undertaken a detailed petrographic and melt inclusion study of the Benfontein Upper, Middle and Lower sills. These sills range in thickness from 0.25 to 5?m. New perovskite and baddeleyite U/Pb dating produced ages of 85.7?±?4.4?Ma and 86.5?±?2.6?Ma, respectively, which are consistent with previous age determinations and indicate emplacement coeval with other kimberlites of the Kimberley cluster. The Benfontein sills are characterised by large variations in texture (e.g., layering) and mineral modal abundance between different sill levels and within individual samples. The Lower Sill is characterised by carbonate-rich diapirs, which intrude into oxide-rich layers from underlying carbonate-rich levels. The general paucity of xenogenic mantle material in the Benfontein sills is attributed to its separation from the host magma during flow differentiation during lateral spreading. The low viscosity is likely responsible for non-explosive emplacement of the Benfontein sills, while the rhythmic layering is attributed to multiple magma injections. The Benfontein sills are marked by the excellent preservation of olivine and groundmass mineralogy, which is composed of monticellite, spinel, perovskite, baddeleyite, ilmenite, apatite, calcite, dolomite along with secondary serpentine and glagolevite [NaMg6[Si3AlO10](OH,O)8•H2O]. This is the first time glagolevite is reported in kimberlites. Groundmass spinel exhibits atoll-textures and is composed of a magnesian ulvöspinel - magnetite (MUM) or chromite core, surrounded by occasional pleonaste and a rim of Mg-Al-magnetite. We suggest that pleonaste crystallised as a magmatic phase, but was resorbed back into the residual host melt and/or removed by alteration. Analyses of secondary inclusions in olivine and primary inclusions in monticellite, spinel, perovskite, apatite and interstitial calcite are largely composed of Ca-Mg carbonates and, to a lesser extent, alkali-carbonates and other phases. These inclusions probably represent the entrapment of variably differentiated parental kimberlite melts, which became progressively more enriched in carbonate, alkalis, halogens and sulphur during crystal fractionation. Carbonate-rich diapirs from the Lower Sill contain more exotic phase assemblages (e.g., Ba-Fe titanate, barite, ancylite, pyrochlore), which probably result from the extreme differentiation of residual kimberlite melts followed by physical separation and isolation from the parental carbonate-rich magma. It is likely that any alkali or halogen rich minerals crystallising in the groundmass were removed from the groundmass during syn?/post-magmatic alteration, or in the case of Na, remobilised to form secondary glagolevite. The Benfontein sill complex therefore provides a unique example of how the composition of kimberlites may be modified after magma emplacement in the upper crust.
Contributions to Mineralogy and Petrology, Vol. 174, 8 22p.
Africa, South Africa, Russia, Canada, Northwest Territories
deposit - Bultfontein, Roberts Victor, Udachnaya-East, Obnazhennaya, Vtorogodnitsa, Koala, Leslie
Abstract: Djerfisherite (K6(Fe,Ni,Cu)25S26Cl) occurs as an accessory phase in the groundmass of many kimberlites, kimberlite-hosted mantle xenoliths, and as a daughter inclusion phase in diamonds and kimberlitic minerals. Djerfisherite typically occurs as replacement of pre-existing Fe-Ni-Cu sulphides (i.e. pyrrhotite, pentlandite and chalcopyrite), but can also occur as individual grains, or as poikilitic phase in the groundmass of kimberlites. In this study, we present new constraints on the origin and genesis of djerfisherite in kimberlites and their entrained xenoliths. Djerfisherite has extremely heterogeneous compositions in terms of Fe, Ni and Cu ratios. However, there appears to be no distinct compositional range of djerfisherite indicative of a particular setting (i.e. kimberlites, xenoliths or diamonds), rather this compositional diversity reflects the composition of the host kimberlite melt and/or interacting metasomatic medium. In addition, djerfisherite may contain K and Cl contents less than the ideal formula unit. Raman spectroscopy and electron backscatter diffraction (EBSD) revealed that these K-Cl poor sulphides still maintain the same djerfisherite crystal structure. Two potential mechanisms for djerfisherite formation are considered: (1) replacement of pre-existing Fe-Ni-Cu sulphides by djerfisherite, which is attributed to precursor sulphides reacting with metasomatic K-Cl bearing melts/fluids in the mantle or the transporting kimberlite melt; (2) direct crystallisation of djerfisherite from the kimberlite melt in groundmass or due to kimberlite melt infiltration into xenoliths. The occurrence of djerfisherite in kimberlites and its mantle cargo from localities worldwide provides strong evidence that the metasomatising/infiltrating kimberlite melt/fluid was enriched in K and Cl. We suggest that kimberlites originated from melts that were more enriched in alkalis and halogens relative to their whole-rock compositions.
Contributions to Mineralogy and Petrology, Vol. 174, 8 22p.
Africa, South Africa, Russia, Canada, Northwest Territories
deposit - Bultfontein, Roberts Victor, Udachnaya-East, Obnazhennaya, Vtorogodnitsa, Koala, Leslie
Abstract: Djerfisherite (K6(Fe,Ni,Cu)25S26Cl) occurs as an accessory phase in the groundmass of many kimberlites, kimberlite-hosted mantle xenoliths, and as a daughter inclusion phase in diamonds and kimberlitic minerals. Djerfisherite typically occurs as replacement of pre-existing Fe-Ni-Cu sulphides (i.e. pyrrhotite, pentlandite and chalcopyrite), but can also occur as individual grains, or as poikilitic phase in the groundmass of kimberlites. In this study, we present new constraints on the origin and genesis of djerfisherite in kimberlites and their entrained xenoliths. Djerfisherite has extremely heterogeneous compositions in terms of Fe, Ni and Cu ratios. However, there appears to be no distinct compositional range of djerfisherite indicative of a particular setting (i.e. kimberlites, xenoliths or diamonds), rather this compositional diversity reflects the composition of the host kimberlite melt and/or interacting metasomatic medium. In addition, djerfisherite may contain K and Cl contents less than the ideal formula unit. Raman spectroscopy and electron backscatter diffraction (EBSD) revealed that these K-Cl poor sulphides still maintain the same djerfisherite crystal structure. Two potential mechanisms for djerfisherite formation are considered: (1) replacement of pre-existing Fe-Ni-Cu sulphides by djerfisherite, which is attributed to precursor sulphides reacting with metasomatic K-Cl bearing melts/fluids in the mantle or the transporting kimberlite melt; (2) direct crystallisation of djerfisherite from the kimberlite melt in groundmass or due to kimberlite melt infiltration into xenoliths. The occurrence of djerfisherite in kimberlites and its mantle cargo from localities worldwide provides strong evidence that the metasomatising/infiltrating kimberlite melt/fluid was enriched in K and Cl. We suggest that kimberlites originated from melts that were more enriched in alkalis and halogens relative to their whole-rock compositions.
Contributions to Mineralogy and Petrology, Vol. 174, 8 22p.
Africa, South Africa, Russia, Canada, Northwest Territories
deposit - Bultfontein, Roberts Victor, Udachnaya-East, Obnazhennaya, Vtorogodnitsa, Koala, Leslie
Abstract: Djerfisherite (K6(Fe,Ni,Cu)25S26Cl) occurs as an accessory phase in the groundmass of many kimberlites, kimberlite-hosted mantle xenoliths, and as a daughter inclusion phase in diamonds and kimberlitic minerals. Djerfisherite typically occurs as replacement of pre-existing Fe-Ni-Cu sulphides (i.e. pyrrhotite, pentlandite and chalcopyrite), but can also occur as individual grains, or as poikilitic phase in the groundmass of kimberlites. In this study, we present new constraints on the origin and genesis of djerfisherite in kimberlites and their entrained xenoliths. Djerfisherite has extremely heterogeneous compositions in terms of Fe, Ni and Cu ratios. However, there appears to be no distinct compositional range of djerfisherite indicative of a particular setting (i.e. kimberlites, xenoliths or diamonds), rather this compositional diversity reflects the composition of the host kimberlite melt and/or interacting metasomatic medium. In addition, djerfisherite may contain K and Cl contents less than the ideal formula unit. Raman spectroscopy and electron backscatter diffraction (EBSD) revealed that these K-Cl poor sulphides still maintain the same djerfisherite crystal structure. Two potential mechanisms for djerfisherite formation are considered: (1) replacement of pre-existing Fe-Ni-Cu sulphides by djerfisherite, which is attributed to precursor sulphides reacting with metasomatic K-Cl bearing melts/fluids in the mantle or the transporting kimberlite melt; (2) direct crystallisation of djerfisherite from the kimberlite melt in groundmass or due to kimberlite melt infiltration into xenoliths. The occurrence of djerfisherite in kimberlites and its mantle cargo from localities worldwide provides strong evidence that the metasomatising/infiltrating kimberlite melt/fluid was enriched in K and Cl. We suggest that kimberlites originated from melts that were more enriched in alkalis and halogens relative to their whole-rock compositions.
Contributions to Mineralogy and Petrology, Vol. 174, 8 22p.
Africa, South Africa, Russia, Canada, Northwest Territories
deposit - Bultfontein, Roberts Victor, Udachnaya-East, Obnazhennaya, Vtorogodnitsa, Koala, Leslie
Abstract: Djerfisherite (K6(Fe,Ni,Cu)25S26Cl) occurs as an accessory phase in the groundmass of many kimberlites, kimberlite-hosted mantle xenoliths, and as a daughter inclusion phase in diamonds and kimberlitic minerals. Djerfisherite typically occurs as replacement of pre-existing Fe-Ni-Cu sulphides (i.e. pyrrhotite, pentlandite and chalcopyrite), but can also occur as individual grains, or as poikilitic phase in the groundmass of kimberlites. In this study, we present new constraints on the origin and genesis of djerfisherite in kimberlites and their entrained xenoliths. Djerfisherite has extremely heterogeneous compositions in terms of Fe, Ni and Cu ratios. However, there appears to be no distinct compositional range of djerfisherite indicative of a particular setting (i.e. kimberlites, xenoliths or diamonds), rather this compositional diversity reflects the composition of the host kimberlite melt and/or interacting metasomatic medium. In addition, djerfisherite may contain K and Cl contents less than the ideal formula unit. Raman spectroscopy and electron backscatter diffraction (EBSD) revealed that these K-Cl poor sulphides still maintain the same djerfisherite crystal structure. Two potential mechanisms for djerfisherite formation are considered: (1) replacement of pre-existing Fe-Ni-Cu sulphides by djerfisherite, which is attributed to precursor sulphides reacting with metasomatic K-Cl bearing melts/fluids in the mantle or the transporting kimberlite melt; (2) direct crystallisation of djerfisherite from the kimberlite melt in groundmass or due to kimberlite melt infiltration into xenoliths. The occurrence of djerfisherite in kimberlites and its mantle cargo from localities worldwide provides strong evidence that the metasomatising/infiltrating kimberlite melt/fluid was enriched in K and Cl. We suggest that kimberlites originated from melts that were more enriched in alkalis and halogens relative to their whole-rock compositions.
Contributions to Mineralogy and Petrology, Vol. 174, 8 22p.
Africa, South Africa, Russia, Canada, Northwest Territories
deposit - Bultfontein, Roberts Victor, Udachnaya-East, Obnazhennaya, Vtorogodnitsa, Koala, Leslie
Abstract: Djerfisherite (K6(Fe,Ni,Cu)25S26Cl) occurs as an accessory phase in the groundmass of many kimberlites, kimberlite-hosted mantle xenoliths, and as a daughter inclusion phase in diamonds and kimberlitic minerals. Djerfisherite typically occurs as replacement of pre-existing Fe-Ni-Cu sulphides (i.e. pyrrhotite, pentlandite and chalcopyrite), but can also occur as individual grains, or as poikilitic phase in the groundmass of kimberlites. In this study, we present new constraints on the origin and genesis of djerfisherite in kimberlites and their entrained xenoliths. Djerfisherite has extremely heterogeneous compositions in terms of Fe, Ni and Cu ratios. However, there appears to be no distinct compositional range of djerfisherite indicative of a particular setting (i.e. kimberlites, xenoliths or diamonds), rather this compositional diversity reflects the composition of the host kimberlite melt and/or interacting metasomatic medium. In addition, djerfisherite may contain K and Cl contents less than the ideal formula unit. Raman spectroscopy and electron backscatter diffraction (EBSD) revealed that these K-Cl poor sulphides still maintain the same djerfisherite crystal structure. Two potential mechanisms for djerfisherite formation are considered: (1) replacement of pre-existing Fe-Ni-Cu sulphides by djerfisherite, which is attributed to precursor sulphides reacting with metasomatic K-Cl bearing melts/fluids in the mantle or the transporting kimberlite melt; (2) direct crystallisation of djerfisherite from the kimberlite melt in groundmass or due to kimberlite melt infiltration into xenoliths. The occurrence of djerfisherite in kimberlites and its mantle cargo from localities worldwide provides strong evidence that the metasomatising/infiltrating kimberlite melt/fluid was enriched in K and Cl. We suggest that kimberlites originated from melts that were more enriched in alkalis and halogens relative to their whole-rock compositions.
Contributions to Mineralogy and Petrology, Vol. 174, 8 22p.
Africa, South Africa, Russia, Canada, Northwest Territories
deposit - Bultfontein, Roberts Victor, Udachnaya-East, Obnazhennaya, Vtorogodnitsa, Koala, Leslie
Abstract: Djerfisherite (K6(Fe,Ni,Cu)25S26Cl) occurs as an accessory phase in the groundmass of many kimberlites, kimberlite-hosted mantle xenoliths, and as a daughter inclusion phase in diamonds and kimberlitic minerals. Djerfisherite typically occurs as replacement of pre-existing Fe-Ni-Cu sulphides (i.e. pyrrhotite, pentlandite and chalcopyrite), but can also occur as individual grains, or as poikilitic phase in the groundmass of kimberlites. In this study, we present new constraints on the origin and genesis of djerfisherite in kimberlites and their entrained xenoliths. Djerfisherite has extremely heterogeneous compositions in terms of Fe, Ni and Cu ratios. However, there appears to be no distinct compositional range of djerfisherite indicative of a particular setting (i.e. kimberlites, xenoliths or diamonds), rather this compositional diversity reflects the composition of the host kimberlite melt and/or interacting metasomatic medium. In addition, djerfisherite may contain K and Cl contents less than the ideal formula unit. Raman spectroscopy and electron backscatter diffraction (EBSD) revealed that these K-Cl poor sulphides still maintain the same djerfisherite crystal structure. Two potential mechanisms for djerfisherite formation are considered: (1) replacement of pre-existing Fe-Ni-Cu sulphides by djerfisherite, which is attributed to precursor sulphides reacting with metasomatic K-Cl bearing melts/fluids in the mantle or the transporting kimberlite melt; (2) direct crystallisation of djerfisherite from the kimberlite melt in groundmass or due to kimberlite melt infiltration into xenoliths. The occurrence of djerfisherite in kimberlites and its mantle cargo from localities worldwide provides strong evidence that the metasomatising/infiltrating kimberlite melt/fluid was enriched in K and Cl. We suggest that kimberlites originated from melts that were more enriched in alkalis and halogens relative to their whole-rock compositions.
Abstract: Strontium and Pb isotopic compositions of clinopyroxene (cpx) in selected samples from three well-characterised eclogite suites with oceanic crustal protoliths (Lace/Kaapvaal craton, Orapa/Zimbabwe craton and Koidu/West African craton) were acquired by high-precision isotope dilution thermal ionisation mass spectrometry (ID-TIMS) and in situ multicollector-laser ablation-inductively-coupled plasma mass spectrometry (MC-LA-ICPMS). The aims of this study are twofold: (1) assess their utility to obtain formation or resetting age constraints and identify elemental signatures that enhance the chances of successful age dating, and (2) to confirm the veracity and utility of results obtained by novel MC-LA-ICPMS techniques. Strontium-Pb isotope systematics of eclogitic cpx measured in this study are decoupled and may reflect addition of unsupported radiogenic Sr during seawater alteration or interaction with oceanic sediments in subduction mélanges, and/or disturbance due to mantle metasomatism, to which the more incompatible Pb is more susceptible. Despite a complex history, subsets of samples yield meaningful model dates. Clinopyroxene fractions from Lace with high Pb contents (3-6?ppm), unradiogenic Pb isotopic compositions (206Pb/204Pb?=?13.57-13.52) and low 238U/204Pb (1.0-1.5) give single-stage model Pb dates of 2.90-2.84?Ga. In contrast, samples from Orapa plot to the right of the Geochron and do not yield meaningful Pb model ages. However, these data do define secondary isochrons that can be modelled to yield minimum age constraints on major events affecting the cratonic lithosphere. Within the uncertainties, the resultant 2.18?±?0.45?Ga age obtained for Koidu eclogites reflect disturbance of the Pb isotope system due to subduction beneath the craton linked to the Eburnean orogeny, while they retained their unradiogenic 87Sr/86Sr (0.7016). Similarly, the age for samples from Orapa (2.20?±?0.54?Ga) is interpreted as an overprint age related to Palaeoproterozoic accretion at the western craton margin. Gabbroic eclogites (Eu/Eu*?>?1) with plagioclase-rich protoliths having low time-integrated Rb/Sr and U/Pb retain the least radiogenic Sr and, in part, Pb. High model ? (9.0 to 9.1) for several eclogites from Lace with elevated LREE, Th and Pb abundances reflects ca. 3.0?Ga addition of a sedimentary component, possibly derived from reworking of a high-? basaltic protocrust, as observed on other cratons. We suggest that sample targeting can be usefully guided by fast-throughput in situ LA-ICPMS techniques, which largely yield results identical to ID-TIMS, albeit at lower precision, and which can further help identify kimberlite contamination in the mineral separates used for solution work.
Abstract: Strontium and Pb isotopic compositions of clinopyroxene (cpx) in selected samples from three well-characterised eclogite suites with oceanic crustal protoliths (Lace/Kaapvaal craton, Orapa/Zimbabwe craton and Koidu/West African craton) were acquired by high-precision isotope dilution thermal ionisation mass spectrometry (ID-TIMS) and in situ multicollector-laser ablation-inductively-coupled plasma mass spectrometry (MC-LA-ICPMS). The aims of this study are twofold: (1) assess their utility to obtain formation or resetting age constraints and identify elemental signatures that enhance the chances of successful age dating, and (2) to confirm the veracity and utility of results obtained by novel MC-LA-ICPMS techniques. Strontium-Pb isotope systematics of eclogitic cpx measured in this study are decoupled and may reflect addition of unsupported radiogenic Sr during seawater alteration or interaction with oceanic sediments in subduction mélanges, and/or disturbance due to mantle metasomatism, to which the more incompatible Pb is more susceptible. Despite a complex history, subsets of samples yield meaningful model dates. Clinopyroxene fractions from Lace with high Pb contents (3-6?ppm), unradiogenic Pb isotopic compositions (206Pb/204Pb?=?13.57-13.52) and low 238U/204Pb (1.0-1.5) give single-stage model Pb dates of 2.90-2.84?Ga. In contrast, samples from Orapa plot to the right of the Geochron and do not yield meaningful Pb model ages. However, these data do define secondary isochrons that can be modelled to yield minimum age constraints on major events affecting the cratonic lithosphere. Within the uncertainties, the resultant 2.18?±?0.45?Ga age obtained for Koidu eclogites reflect disturbance of the Pb isotope system due to subduction beneath the craton linked to the Eburnean orogeny, while they retained their unradiogenic 87Sr/86Sr (0.7016). Similarly, the age for samples from Orapa (2.20?±?0.54?Ga) is interpreted as an overprint age related to Palaeoproterozoic accretion at the western craton margin. Gabbroic eclogites (Eu/Eu*?>?1) with plagioclase-rich protoliths having low time-integrated Rb/Sr and U/Pb retain the least radiogenic Sr and, in part, Pb. High model ? (9.0 to 9.1) for several eclogites from Lace with elevated LREE, Th and Pb abundances reflects ca. 3.0?Ga addition of a sedimentary component, possibly derived from reworking of a high-? basaltic protocrust, as observed on other cratons. We suggest that sample targeting can be usefully guided by fast-throughput in situ LA-ICPMS techniques, which largely yield results identical to ID-TIMS, albeit at lower precision, and which can further help identify kimberlite contamination in the mineral separates used for solution work.
Abstract: Strontium and Pb isotopic compositions of clinopyroxene (cpx) in selected samples from three well-characterised eclogite suites with oceanic crustal protoliths (Lace/Kaapvaal craton, Orapa/Zimbabwe craton and Koidu/West African craton) were acquired by high-precision isotope dilution thermal ionisation mass spectrometry (ID-TIMS) and in situ multicollector-laser ablation-inductively-coupled plasma mass spectrometry (MC-LA-ICPMS). The aims of this study are twofold: (1) assess their utility to obtain formation or resetting age constraints and identify elemental signatures that enhance the chances of successful age dating, and (2) to confirm the veracity and utility of results obtained by novel MC-LA-ICPMS techniques. Strontium-Pb isotope systematics of eclogitic cpx measured in this study are decoupled and may reflect addition of unsupported radiogenic Sr during seawater alteration or interaction with oceanic sediments in subduction mélanges, and/or disturbance due to mantle metasomatism, to which the more incompatible Pb is more susceptible. Despite a complex history, subsets of samples yield meaningful model dates. Clinopyroxene fractions from Lace with high Pb contents (3-6?ppm), unradiogenic Pb isotopic compositions (206Pb/204Pb?=?13.57-13.52) and low 238U/204Pb (1.0-1.5) give single-stage model Pb dates of 2.90-2.84?Ga. In contrast, samples from Orapa plot to the right of the Geochron and do not yield meaningful Pb model ages. However, these data do define secondary isochrons that can be modelled to yield minimum age constraints on major events affecting the cratonic lithosphere. Within the uncertainties, the resultant 2.18?±?0.45?Ga age obtained for Koidu eclogites reflect disturbance of the Pb isotope system due to subduction beneath the craton linked to the Eburnean orogeny, while they retained their unradiogenic 87Sr/86Sr (0.7016). Similarly, the age for samples from Orapa (2.20?±?0.54?Ga) is interpreted as an overprint age related to Palaeoproterozoic accretion at the western craton margin. Gabbroic eclogites (Eu/Eu*?>?1) with plagioclase-rich protoliths having low time-integrated Rb/Sr and U/Pb retain the least radiogenic Sr and, in part, Pb. High model ? (9.0 to 9.1) for several eclogites from Lace with elevated LREE, Th and Pb abundances reflects ca. 3.0?Ga addition of a sedimentary component, possibly derived from reworking of a high-? basaltic protocrust, as observed on other cratons. We suggest that sample targeting can be usefully guided by fast-throughput in situ LA-ICPMS techniques, which largely yield results identical to ID-TIMS, albeit at lower precision, and which can further help identify kimberlite contamination in the mineral separates used for solution work.
A geochemical and Nd, Sr and stable Ca isotopic study of carbonatites and associated silicate rocks from the ~65 Ma old Ambadongar carbonatite complex and the Phenai Mata igneous complex, Gujarat, India: implications for crustal contamination, carbonate r
Earth and Planetary Science Letters, Vol. 506, pp. 15-26.
Africa, South Africa
deposit - Newlands, Kimberley, Bultfontein
Abstract: MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) and PIC (Phlogopite-Ilmenite-Clinopyroxene) rocks occur as mantle-derived xenoliths in kimberlites and other alkaline volcanic rocks. Both rock types are alkaline and ultramafic in composition. The H2O and alkali metal enrichments in MARID and PIC rocks, reflected in abundant phlogopite, have been suggested to be caused by extreme mantle metasomatism. Radiogenic (Sr-Nd-Hf-Pb) isotope and trace element compositions for mineral separates from MARID (clinopyroxene and amphibole) and PIC (clinopyroxene only) samples derived from Cretaceous kimberlites (Kimberley) and orangeites (Newlands) from South Africa are used here to examine the source(s) of mantle metasomatism. PIC clinopyroxene is relatively homogeneous, with narrow ranges in initial isotopic composition (calculated to the emplacement age of the host Bultfontein kimberlite; 87Sr/86Sri: 0.7037-0.7041; ?Ndi: +3.0 to +3.6; ?Hfi: +2.2 to +2.5; 206Pb/204Pbi: 19.72-19.94) similar to kimberlite values. This is consistent with PIC rocks representing peridotites modified by intense metasomatic interaction with kimberlite melts. The MARID clinopyroxene and amphibole separates () studied here display broader ranges in isotope composition (e.g., 87Sr/86Sri: 0.705-0.711; ?Ndi: ?11.0 to ?1.0; ?Hfi: ?17.9 to ?8.5; 206Pb/204Pbi: 17.33-18.72) than observed in previous studies of MARID rocks. The Nd-Hf isotope compositions of kimberlite-derived MARID samples fall below the mantle array (??Hfi between ?13.0 and ?2.4), a feature reported widely for kimberlites and other alkaline magmas. We propose that such displacements in MARID minerals result from metasomatic alteration of an initial “enriched mantle” MARID composition (i.e., 87Sr/86Sri = 0.711; ?Ndi = ?11.0; ?Hfi = ?17.9; and 206Pb/204Pbi = 17.3) by the entraining kimberlite magma (87Sr/86Sr; ?Nd; ?Hf; 206Pb/204Pb). A model simulating the flow of kimberlite magma through a mantle column, thereby gradually equilibrating the isotopic and chemical compositions of the MARID wall-rock with those of the kimberlite magma, broadly reproduces the Sr-Nd-Hf-Pb isotope compositions of the MARID minerals analysed here. This model also suggests that assimilation of MARID components could be responsible for negative ??Hfi values in kimberlites. The isotopic composition of the inferred initial MARID end-member, with high 87Sr/86Sr and low ?Nd, ?Hf, and 206Pb/204Pb, resembles those found in orangeites, supporting previous inferences of a genetic link between MARID-veined mantle and orangeites. The metasomatic agent that produced such compositions in MARID rocks must be more extreme than the EM-II mantle component and may relate to recycled material that experienced long-term storage in the lithospheric mantle.
Earth and Planetary Science Letters, Vol. 506, pp. 15-26.
Africa, South Africa
deposit - Newlands, Kimberley, Bultfontein
Abstract: MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) and PIC (Phlogopite-Ilmenite-Clinopyroxene) rocks occur as mantle-derived xenoliths in kimberlites and other alkaline volcanic rocks. Both rock types are alkaline and ultramafic in composition. The H2O and alkali metal enrichments in MARID and PIC rocks, reflected in abundant phlogopite, have been suggested to be caused by extreme mantle metasomatism. Radiogenic (Sr-Nd-Hf-Pb) isotope and trace element compositions for mineral separates from MARID (clinopyroxene and amphibole) and PIC (clinopyroxene only) samples derived from Cretaceous kimberlites (Kimberley) and orangeites (Newlands) from South Africa are used here to examine the source(s) of mantle metasomatism. PIC clinopyroxene is relatively homogeneous, with narrow ranges in initial isotopic composition (calculated to the emplacement age of the host Bultfontein kimberlite; 87Sr/86Sri: 0.7037-0.7041; ?Ndi: +3.0 to +3.6; ?Hfi: +2.2 to +2.5; 206Pb/204Pbi: 19.72-19.94) similar to kimberlite values. This is consistent with PIC rocks representing peridotites modified by intense metasomatic interaction with kimberlite melts. The MARID clinopyroxene and amphibole separates () studied here display broader ranges in isotope composition (e.g., 87Sr/86Sri: 0.705-0.711; ?Ndi: ?11.0 to ?1.0; ?Hfi: ?17.9 to ?8.5; 206Pb/204Pbi: 17.33-18.72) than observed in previous studies of MARID rocks. The Nd-Hf isotope compositions of kimberlite-derived MARID samples fall below the mantle array (??Hfi between ?13.0 and ?2.4), a feature reported widely for kimberlites and other alkaline magmas. We propose that such displacements in MARID minerals result from metasomatic alteration of an initial “enriched mantle” MARID composition (i.e., 87Sr/86Sri = 0.711; ?Ndi = ?11.0; ?Hfi = ?17.9; and 206Pb/204Pbi = 17.3) by the entraining kimberlite magma (87Sr/86Sr; ?Nd; ?Hf; 206Pb/204Pb). A model simulating the flow of kimberlite magma through a mantle column, thereby gradually equilibrating the isotopic and chemical compositions of the MARID wall-rock with those of the kimberlite magma, broadly reproduces the Sr-Nd-Hf-Pb isotope compositions of the MARID minerals analysed here. This model also suggests that assimilation of MARID components could be responsible for negative ??Hfi values in kimberlites. The isotopic composition of the inferred initial MARID end-member, with high 87Sr/86Sr and low ?Nd, ?Hf, and 206Pb/204Pb, resembles those found in orangeites, supporting previous inferences of a genetic link between MARID-veined mantle and orangeites. The metasomatic agent that produced such compositions in MARID rocks must be more extreme than the EM-II mantle component and may relate to recycled material that experienced long-term storage in the lithospheric mantle.
Earth and Planetary Science Letters, Vol. 506, pp. 15-26.
Africa, South Africa
deposit - Newlands, Kimberley, Bultfontein
Abstract: MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) and PIC (Phlogopite-Ilmenite-Clinopyroxene) rocks occur as mantle-derived xenoliths in kimberlites and other alkaline volcanic rocks. Both rock types are alkaline and ultramafic in composition. The H2O and alkali metal enrichments in MARID and PIC rocks, reflected in abundant phlogopite, have been suggested to be caused by extreme mantle metasomatism. Radiogenic (Sr-Nd-Hf-Pb) isotope and trace element compositions for mineral separates from MARID (clinopyroxene and amphibole) and PIC (clinopyroxene only) samples derived from Cretaceous kimberlites (Kimberley) and orangeites (Newlands) from South Africa are used here to examine the source(s) of mantle metasomatism. PIC clinopyroxene is relatively homogeneous, with narrow ranges in initial isotopic composition (calculated to the emplacement age of the host Bultfontein kimberlite; 87Sr/86Sri: 0.7037-0.7041; ?Ndi: +3.0 to +3.6; ?Hfi: +2.2 to +2.5; 206Pb/204Pbi: 19.72-19.94) similar to kimberlite values. This is consistent with PIC rocks representing peridotites modified by intense metasomatic interaction with kimberlite melts. The MARID clinopyroxene and amphibole separates () studied here display broader ranges in isotope composition (e.g., 87Sr/86Sri: 0.705-0.711; ?Ndi: ?11.0 to ?1.0; ?Hfi: ?17.9 to ?8.5; 206Pb/204Pbi: 17.33-18.72) than observed in previous studies of MARID rocks. The Nd-Hf isotope compositions of kimberlite-derived MARID samples fall below the mantle array (??Hfi between ?13.0 and ?2.4), a feature reported widely for kimberlites and other alkaline magmas. We propose that such displacements in MARID minerals result from metasomatic alteration of an initial “enriched mantle” MARID composition (i.e., 87Sr/86Sri = 0.711; ?Ndi = ?11.0; ?Hfi = ?17.9; and 206Pb/204Pbi = 17.3) by the entraining kimberlite magma (87Sr/86Sr; ?Nd; ?Hf; 206Pb/204Pb). A model simulating the flow of kimberlite magma through a mantle column, thereby gradually equilibrating the isotopic and chemical compositions of the MARID wall-rock with those of the kimberlite magma, broadly reproduces the Sr-Nd-Hf-Pb isotope compositions of the MARID minerals analysed here. This model also suggests that assimilation of MARID components could be responsible for negative ??Hfi values in kimberlites. The isotopic composition of the inferred initial MARID end-member, with high 87Sr/86Sr and low ?Nd, ?Hf, and 206Pb/204Pb, resembles those found in orangeites, supporting previous inferences of a genetic link between MARID-veined mantle and orangeites. The metasomatic agent that produced such compositions in MARID rocks must be more extreme than the EM-II mantle component and may relate to recycled material that experienced long-term storage in the lithospheric mantle.
Abstract: A detailed electron microprobe study has been carried out on the compositional variations of mica and apatite from carbonatites, phoscorites and associated pyroxenites (and fenites) of the Loolekop deposit, Palabora Carbonatite Complex (South Africa). Mica in pyroxenites and fenites is Mg-rich biotite, whilst micas in carbonatites and phoscorites are compositionally diverse including phlogopite, Ba-rich phlogopite (up to 30% kinoshitalite component), IVAl-rich phlogopite (up to 30% eastonite component) and tetraferriphlogopite. The various types of phlogopites are interpreted as orthomagmatic phases, whereas tetraferriphlogopite precipitation was a late-magmatic to hydrothermal process that additionally introduced REE into the system. Orthomagmatic apatite is generally REE- and Sr-poor fluorapatite and does not show large compositional differences between rock types. Apatite associated with the late-stage tetraferriphlogopite mineralization reaches higher levels of REE (up to 4.9?wt%), Si (up to 1.5?wt% SiO2), Sr (up to 2.6?wt% SrO) and Na (up to 1.0?wt% Na2O). The compositional variation of micas and apatites, which is affiliated with distinct rock types, reflects the multi-stage evolution of the Loolekop deposit and provides detailed insight into the relationships of the carbonatite-phoscorite assemblage. The obtained data support the separation of phoscorite and carbonatite by immiscibility from a common parental magma, which may happen due to a decrease of temperature and/or pressure during the ascent of the magma. This results in a density contrast between the carbonatitic and phoscoritic components that will lead to descending phoscorite accumulations at the outer zones of the magma channel and a jet-like ascent (further promoted by its extremely low viscosity) of the carbonatite magma. The genetic model deduced here explains the peculiar association of carbonatites, phoscorites and silicate rocks in many alkaline complexes worldwide.
University of Alberta, Msc thesis https://doi.org /10.7939/R3NC5SV24 available
Canada, Nunavut
deposit - Darby
Abstract: The Rae Craton, northern Canada, contains several diamondiferous kimberlite fields that have been a focus of episodic diamond exploration. Relatively little is known about the deep mantle lithosphere underpinning the architecturally complex crust. We present bulk and mineral element and isotopic compositional data for peridotite and pyroxenite/eclogite xenoliths from the Darby kimberlites representing fragments of the west central Rae lithosphere, as well as the first kimberlite eruption age of 542.2±2.6 Ma (2 ?; phlogopite Rb-Sr isochron). Darby peridotites have low bulk Al2O3 contents with highly-depleted olivine (median Mg#?=?92.5) characteristic of cratonic lithosphere globally, but more depleted than peridotites from other Rae Craton localities. One peridotite xenolith contains a harzburgitic G10D garnet. Re-Os TRD model ages appear to be the oldest measured to date from peridotites of the Rae lithosphere, having a mode in the early Neoarchean and ranging to the Paleoproterozoic (~2.3 Ga). Concentrate clinopyroxene defines a well constrained mantle geotherm indicating the existence of a ~200 km thick lithosphere at the time of kimberlite eruption, greater than the lithospheric thickness beneath Somerset Island and in good agreement with modern seismic constraints. Nickel-in-garnet thermometry in grains that record temperatures below the mantle adiabat, indicates mantle sampling dominantly in the graphite stability field whereas Al-in-olivine thermometry shows a distinct mantle sampling mode in the diamond stability field. Abundant pyroxenite and eclogite xenoliths are recovered across the Darby property and low-Cr garnet (Cr2O3?
Geochimica et Cosmochimica Acta, Vol. 224, pp. 132-153.
Russia, Siberia
deposit - Obnazhennaya
Abstract: The Obnazhennaya kimberlite in the NE Siberian craton hosts a most unusual cratonic xenolith suite, with common rocks rich in pyroxenes and garnet, and no sheared peridotites. We report petrographic and chemical data for whole rocks (WR) and minerals of 20 spinel and garnet peridotites from Obnazhennaya with Re-depletion Os isotope ages of 1.8-2.9?Ga (Ionov et al., 2015a) as well as 2 pyroxenites. The garnet-bearing rocks equilibrated at 1.6-2.8?GPa and 710-1050?°C. Some xenoliths contain vermicular spinel-pyroxene aggregates with REE patterns in clinopyroxene mimicking those of garnet. The peridotites show significant scatter of Mg# (0.888-0.924), Cr2O3 (0.2-1.4?wt.%) and high NiO (0.3-0.4?wt.%). None are pristine melting residues. Low-CaO-Al2O3 (?0.9?wt.%) dunites and harzburgites are melt-channel materials. Peridotites with low to moderate Al2O3 (0.4-1.8?wt.%) usually have CaO?>?Al2O3, and some have pockets of calcite texturally equilibrated with olivine and garnet. Such carbonates, exceptional in mantle xenoliths and reported here for the first time for the Siberian mantle, provide direct evidence for modal makeover and Ca and LREE enrichments by ephemeral carbonate-rich melts. Peridotites rich in CaO and Al2O3 (2.7-8.0?wt.%) formed by reaction with silicate melts. We infer that the mantle lithosphere beneath Obnazhennaya, initially formed in the Mesoarchean, has been profoundly modified. Pervasive inter-granular percolation of highly mobile and reactive carbonate-rich liquids may have reduced the strength of the mantle lithosphere leading the way for reworking by silicate melts. The latest events before the kimberlite eruption were the formation of the carbonate-phlogopite pockets, fine-grained pyroxenite veins and spinel-pyroxene symplectites. The reworked lithospheric sections are preserved at Obnazhennaya, but similar processes could erode lithospheric roots in the SE Siberian craton (Tok) and the North China craton, where ancient melting residues and reworked garnet-bearing peridotites are absent. The modal, chemical and Os-isotope compositions of the Obnazhennaya xenoliths produced by reaction of refractory peridotites with melts are very particular (high Ca/Al, no Mg#-Al correlations, highly variable Cr, low 187Os/188Os, continuous modal range from olivine-rich to low-olivine peridotites, wehrlites and websterites) and distinct from those of fertile lherzolites in off-craton xenoliths and peridotite massifs. These features argue against the concept of ‘refertilization’ of cratonic and other refractory peridotites by mantle-derived melts as a major mechanism to form fertile to moderately depleted lherzolites in continental lithosphere. The Obnazhennaya xenoliths represent a natural rock series produced by ‘refertilization’, but include no rocks equivalent in modal, major and trace element to the fertile lherzolites. This study shows that ‘refertilization’ yields broad, continuous ranges of modal and chemical compositions with common wehrlites and websterites that are rare among off-craton xenoliths.
Abstract: The oxidation state of iron in Earth’s mantle is well known to depths of approximately 200?km, but has not been characterized in samples from the lowermost upper mantle (200-410?km depth) or the transition zone (410-660?km depth). Natural samples from the deep (>200?km) mantle are extremely rare, and are usually only found as inclusions in diamonds. Here we use synchrotron Mössbauer source spectroscopy complemented by single-crystal X-ray diffraction to measure the oxidation state of Fe in inclusions of ultra-high pressure majoritic garnet in diamond. The garnets show a pronounced increase in oxidation state with depth, with Fe3+/(Fe3++ Fe2+) increasing from 0.08 at approximately 240?km depth to 0.30 at approximately 500?km depth. The latter majorites, which come from pyroxenitic bulk compositions, are twice as rich in Fe3+ as the most oxidized garnets from the shallow mantle. Corresponding oxygen fugacities are above the upper stability limit of Fe metal. This implies that the increase in oxidation state is unconnected to disproportionation of Fe2+ to Fe3+ plus Fe0. Instead, the Fe3+ increase with depth is consistent with the hypothesis that carbonated fluids or melts are the oxidizing agents responsible for the high Fe3+ contents of the inclusions.
Abstract: Quantitative trace element data from high-purity gem diamonds from the Victor Mine, Ontario, Canada as well as near-gem diamonds from peridotite and eclogite xenoliths from the Finsch and Newlands mines, South Africa, acquired using an off-line laser ablation method show that we see the same spectrum of fluids in both high-purity gem and near-gem diamonds that was previously documented in fibrous diamonds. "Planed" and "ribbed" trace element patterns characterize not only the high-density fluid (HDF) inclusions in fibrous diamonds but also in gem diamonds. Two diamonds from two Finsch harzburgite xenoliths show trace element patterns similar to those of saline fluids, documenting the involvement of saline fluids in the precipitation of gem diamonds, further strengthening the link between the parental fluids of both gem and fibrous diamonds. Differences in trace element characteristics are evident between Victor diamonds containing silicate inclusions compared with Victor diamonds containing sulphide inclusions. The sulphide-bearing diamonds show lower levels of inter-element fractionation and more widely varying siderophile element concentrations - indicating that the silicate and sulphide-bearing diamonds likely formed by gradations of the same processes, via melt-rock reaction or from a subtly different fluid source. The shallow negative LREEN-HREEN slopes displayed by the Victor diamonds establish a signature indicative of original derivation of the diamond forming agent during major melting (~10% melt). Consequently, this signature must have been passed on to HDFs separating from such silicate melts.
Abstract: Quantitative trace element data from high-purity gem diamonds from the Victor Mine, Ontario, Canada as well as near-gem diamonds from peridotite and eclogite xenoliths from the Finsch and Newlands mines, South Africa, acquired using an off-line laser ablation method show that we see the same spectrum of fluids in both high-purity gem and near-gem diamonds that was previously documented in fibrous diamonds. "Planed" and "ribbed" trace element patterns characterize not only the high-density fluid (HDF) inclusions in fibrous diamonds but also in gem diamonds. Two diamonds from two Finsch harzburgite xenoliths show trace element patterns similar to those of saline fluids, documenting the involvement of saline fluids in the precipitation of gem diamonds, further strengthening the link between the parental fluids of both gem and fibrous diamonds. Differences in trace element characteristics are evident between Victor diamonds containing silicate inclusions compared with Victor diamonds containing sulphide inclusions. The sulphide-bearing diamonds show lower levels of inter-element fractionation and more widely varying siderophile element concentrations - indicating that the silicate and sulphide-bearing diamonds likely formed by gradations of the same processes, via melt-rock reaction or from a subtly different fluid source. The shallow negative LREEN-HREEN slopes displayed by the Victor diamonds establish a signature indicative of original derivation of the diamond forming agent during major melting (~10% melt). Consequently, this signature must have been passed on to HDFs separating from such silicate melts.
Abstract: At the core of many Earth-scale processes is the question of what the deep mantle is made of. The only direct samples from such extreme depths are diamonds and their inclusions. It is commonly assumed that these inclusions reflect ambient mantle or are syngenetic with diamond, but these assumptions are rarely tested. We have studied inclusion-host growth relationships in two potentially superdeep diamonds from Juina (Brazil) containing nine inclusions of Fe-rich (XFe ?0.33 to ?0.64) ferropericlase-magnesiowüstite (FM) by X-ray diffractometry, X-ray tomography, cathodoluminescence, electron backscatter diffraction, and electron microprobe analysis. The inclusions share a common [112] zone axis with their diamonds and have their major crystallographic axes within 3°-8° of those of their hosts. This suggests a specific crystallographic orientation relationship (COR) resulting from interfacial energy minimization, disturbed by minor post-entrapment rotation around [112] due to plastic deformation. The observed COR and the relationships between inclusions and diamond growth zones imply that FM nucleated during the growth history of the diamond. Therefore, these inclusions may not provide direct information on the ambient mantle prior to diamond formation. Consequently, a “non-pyrolitic” composition of the lower mantle is not required to explain the occurrence of Fe-rich FM inclusions in diamonds. By identifying examples of mineral inclusions that reflect the local environment of diamond formation and not ambient mantle, we provide both a cautionary tale and a means to test diamond-inclusion time relationships for proper application of inclusion studies to whole-mantle questions.
Journal of Asian Earth Sciences, Vol. 172, pp. 56-65.
China, Mongolia
deposit - Bayan Obo
Abstract: In the Bayan Obo REE deposit in Inner Mongolia, Northern China, three major orebodies are hosted in dolomite marble of the Bayan Obo Group. There are carbonatite dikes in the ore district. Apatite is a common accessary mineral in the ore-hosting dolomite marble (DM apatite) and in carbonatite dikes (IC apatite). These two types of apatite are both fluorapatite, and have low SiO2, uniform P2O5, and variable CaO contents. Total REY (REEs?+?Y) contents are correlated with Na2O contents, indicating that REY of both types of apatite enter lattice via the substitution reaction: Na+ + (REY)3+ = 2Ca2+. These features, combined with high REY (6230-18,906?ppm) and Sr (9653-17,200?ppm) contents of DM apatite, indicate that DM apatite likely had a carbonatite origin. Some DM apatite grains are partially replaced by albite and quartz. Fluid inclusions crosscutting both apatite and albite or quartz indicate that they formed later than quartz and albite replacement. The back-scattered electron images show that DM apatite grains contain many micro-pores (fluid inclusions), and monazite inclusions formed from the fluid inclusions. However, no monazite inclusions are observed within quartz and albite, excluding the possibility that the monazite inclusions were precipitated directly from the fluids. The monazite inclusions were therefore formed during fluid-induced dissolution-reprecipitation processes, where DM apatite served as the source of LREEs. This also explains the depletion of some LREEs in DM apatite. The formation of monazite inclusions in apatite requires fluids with relatively low Na and Si concentrations, different from the fluids responsible for quartz and albite replacement. DM apatite was affected by two stages of fluid activities: the first stage of metasomatism by alkaline fluids that were likely derived from carbonatite magmas when the deposit first formed (represented by quartz and albite replacement), followed by a second stage of modification that caused LREEs depletion and the formation of new REE minerals. Thus, the Bayan Obo REE ore deposit was modified by a significant thermal event after the formation, which provided negligible or only small amounts of REEs.
Abstract: The Siberian Craton was assembled in a Paleoproterozoic episode at about 1.88?Ga by the collision of older blocks, followed at about 1.86?Ga by post-collisional felsic magmatism. We have found a set of extremely fresh mica-bearing lamprophyre-looking rocks within the Sharyzhalgay metamorphic complex of the south-western Siberian Craton. Zircon from these rocks yields a UPb TIMS age of 1864.7?±?1.8?Ma, which coincides perfectly with the peak of the post-collisional granite ages and postdates by ~15?Ma the peak of ages obtained for metamorphism. The same ages were reported earlier for a mafic dyke with ocean island basalt (OIB) geochemical signatures and a Pt-bearing mafic-ultramafic intrusion found in the same region. Mineralogy, major and trace element geochemistry and Sr-Nd-Pb isotopes show that the studied rocks (1) have shoshonitic affinity, (2) are hybrid rocks with mineral assemblages which could not be in equilibrium, (3) where derived by recycling of an Archean crustal source and (4) resemble post-collision Tibetan shoshonitic series. The genesis of these rocks is considered to be due to melting of crustal lithologies and metasomatized lithospheric mantle within a subducted slab. Some of the resulting melts ascended through the lithospheric column and fractionated to low-Mg absarokites, whereas other melts were contaminated by orthopyroxenitic mantle material and attained unusual high-Mg mafic compositions. According to our model, the post-collisional magmatism (shoshonite- and OIB-type) occurred due to upwelling of hot asthenosphere through a slab window, when the active collision ceased as a result of the slab break off and loss of the slab pull force. Overall, our study shows that in the Paleoproterozoic shoshonitic melts were emplaced within a similar tectonic setting as seen today in modern orogenic systems.
Abstract: We describe the mineralogy of a lamproite dyke from Gundrapalli village (Nalgonda district), Telangana, India. The dyke consists of a mineral assemblage characteristic of lamproites in terms of the presence of amphiboles (mainly potassic-richterite together with potassic-arfvedsonite, magnesio-riebeckite, Ti-rich potassic-magnesio-arfvedsonite, potassic-magnesio-arfvedsonite, katophorite and potassic-ferri-katophorite), Al-poor pyroxene, phlogopite (Ti-rich, Al-poor), pseudomorphed leucite, spinel (chromite-magnesiochromite), fluoroapatite, barite, titanite, rutile, baritocalcite, calcite, ilmenite, hydro-zircon, baotite, strontianite, allanite, quartz and pyrite. The absence of wadeite and priderite have been compensated for by presence of baotite, rutile, titanite, barite, and hydro-zircons. The presence of the secondary phases: allanite, hydro-zircon, chlorite, quartz, and cryptocrystalline silica, implies that the dyke has undergone deuteric alteration. The Gundrapalli dyke on the basis of its typomorphic mineralogy has been classified as a pseudoleucite-phlogopite-amphibole-lamproite. We report the presence of the rare mineral baotite from this lamproite, the first recognition of baotite from a lamproite in India. The mineralogy of the baotite- bearing Gundrapalli lamproite is analogous to the baotite- bearing Kvaløya lamproite from Troms, Norway. Ultrapotassic magmatism is quite prevalent in the Eastern Dharwar Complex of south India. Numerous new finds of lamproite dykes from and around the Palaeo-Mesoproterozoic Cuddapah basin gives an opportunity to understand the nature of the subcontinental lithospheric mantle in southern India. We present the mineralogy of a newly discovered lamproite dyke at Gundrapalli village (Nalgonda district) northwest of Cuddapah basin (Figure 1 inset). The lamproite dyke at Gundrapalli village, intruded into the Paleoproterozoic biotite granite unit of Peninsular Gneissic Complex form part of eastern Dharwar Complex. (Figure 1; Kumar et al., 2013, Ahmed et al., 2012).
Abstract: Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) and commercially-available HyMap hyperspectral data were used to study the occurrence and mineralogical characteristics of limberlite diatremes in the State-Line district of Colorado/Wyoming. A mosaic of five flightlines of AVIRIS data acquired during 1996 with 20-m resolution is being used to locate and characterize the kimberlite diatremes. Higher spatial resolution data (1.6 m AVIRIS and 4m HyMap acquired in 1998 and 1999, respectively) are being used to map additional detail. Poor exposures, vegetation cover, and weathering, however, make identification of characteristic kimberlite minerals difficult except where exposed by mining. Minerals identified in the district using the hyperspectral data include calcite, dolomite, illite/muscovite, and serpentine (principally antigorite), however, most spectral signatures are dominated by both green and dry vegetation. The goal of this work is to determine methods for characterizing subtle mineralogic changes associated with kimberlites as a guide to exploration in a variety of geologic terrains.
Abstract: The Gifford Creek Carbonatite Complex (GCCC), Western Australia contains a diverse suite of alkaline igneous rocks, including magnesiocarbonatites, ferrocarbonatites, phoscorites, fenites, magmatic-hydrothermal peralkaline dykes, and ironstones. This study employs U-Pb, Sm-Nd, and Lu-Hf radiogenic isotope techniques on monazite - (Ce), fluorapatite, and zircon to determine the origin, age, and history of the GCCC. Zircon crystals found in glimmerite alteration selvages adjacent to ferrocarbonatites exhibit pyramidal crystal morphologies, ?Hf values of ?1.8 to ?4.3, high Th/U, and variable Zr/Hf, all of which are indicative of carbonatitic zircon sourced from an enriched mantle component. Uranium-Pb dating of these zircons returned a definitive magmatic age of ~1370?Ma for the GCCC. Monazite hosted in the ferrocarbonatites, phoscorites, and fenite alteration assemblages yielded variable U-Pb ages ranging from ca. 1250?Ma to 815?Ma. Neodymium isotope isochrons determined from coexisting monazite and apatite gave ages between ca. 1310?Ma to ca. 1190?Ma, but all with similar initial 143Nd/144Nd values of 0.51078-0.51087. The 1370?Ma age of the GCCC does not correspond to any known mantle plume activity, but does broadly correlate with the separation of the North China Craton from the West Australian Craton as part of the greater breakup of Nuna. The monazite and apatite ?Nd data illustrate that the multiple younger U-Pb monazite and Nd isotope isochron ages are not recording multiple magmatic intrusions into the complex, but rather represent partial recrystallisation/resetting of REE-bearing minerals during the protracted tectonic history of the Western Australia Craton from ~1300?Ma to 815?Ma and its involvement in the breakup of Nuna and assembly and disassembly of Rodinia. The age variability in the U-Pb and the Sm-Nd isotope systems in monazite and apatite reveal that tectonically-induced hydrothermalism can contribute to the isotopic resetting of phosphate minerals. This age resetting, if properly identified, can be used as a thorough geochronological record of tectonism affecting alkaline igneous complexes after initial magmatic emplacement.
Abstract: The Rosário-6 is a non-diamondiferous hypabyssal kimberlite located above the Rio de la Plata craton and near the south-eastern edge of the Paraná Basin, in southern Brazil. It is petrographically an inequigranular texture, macrocrystal kimberlite, fresh and the groundmass exhibits a microporphyritic texture and round megacrysts of olivine, which are derived from disaggregated mantle xenoliths. Olivine is also present as macrocrysts, microphenocrysts and in the groundmass together with phlogopite and apatite. These microphenocrysts are immersed in a groundmass of olivine, monticellite, phlogopite, CaTiO3-perovskite, apatite, Mg-chromite and Mg-ulvöspinel and melilite. A mesostasis assemblage of phlogopite, melilite, soda melilite, akermanite and calcium carbonate is segregated from the groundmass. Its geochemical signature is similar to those of transitional kimberlites of Kaapvaal Craton, South Africa, and the U-Pb ages of ~ 128 Ma on perovskite reveal that Rosário-6 kimberlite post-dates the main pulse of volcanism in the Paraná-Etendeka Large Igneous Province (LIP). The high Ti content of some minerals, such as Mg-chromite, Mg-ulvöspinel, phlogopite and melilite, and the presence of perovskite suggest a Ti-rich source. The petrographic, geochemical and isotopic data indicate that the Rosário-6 kimberlite source is a depleted mantle metasomatized by H2O-rich fluids, CO2-rich and silicate melts derived from the recycling of an ancient subducted oceanic plate (eclogite) before the South Atlantic opening. Although several authors indicate the influence of Tristan da Cunha plume for the generation of alkaline magmatism associated to the Paraná-Etendeka flood basalts, our data demonstrates that Tristan da Cunha plume has no chemical contribution to the generation of Rosário-6 kimberlite, except by its thermal influence.
Earth and Planetary Science Letters, Vol. 510, pp. 219-230.
Africa, Tanzania
deposit - Oldoinyo Lengai
Abstract: Historic eruptions of Earth's only active carbonatite volcano, Oldoinyo Lengai (Tanzania), have repeatedly switched from low energy carbonatite lava extrusion to highly energetic explosive silicate volcanism, most recently in 1966-67 and 2007-08. The explosive eruptions produce strongly Si-undersaturated peralkaline silicate ashes with unusually high (Na + K)/Al of 3.4-6.3 when compared to the average peralkalinity of ?0.8 in the East African Rift System. A series of experiments in the carbonatite-clinopyroxene system at 750-1150 °C, 0.1 GPa, reveal that augitic clinopyroxene breaks down peritectically at >900 °C yielding strongly peralkaline conjugated silicate- and carbonatite melts. The clinopyroxene-derived silicate melt dissolves (Na,K)2O from the (Na,K)2CO3-component of the carbonatite leading to high peralkalinities and to liberation of excess CO2, since the solubility of carbon dioxide in silicate liquids is ?1 wt.% at subvolcanic pressures. Carbonatite injection into subvolcanic clinopyroxene-rich crystal mushes hence explains the occurrence of strongly peralkaline silicate melts and provides a mechanism for CO2-driven explosive eruptions. The silicate melt compositions mostly depend on the (Na + K)/Ca ratio of the intruding carbonatite, the silicate ashes erupted in 1966-67 and 2007-08 require an interaction of a clinopyroxene-rich crystal mush with a slightly less evolved alkali-carbonatite than presently erupted at Oldoinyo Lengai. The mechanism identified here, where mineral breakdown induced melt hybridization triggers volatile saturation and highly explosive volcanism is generally applicable to igneous systems that involve carbonatites or other low-viscosity CO2-bearing alkaline silicate melts.
Contributions to Mineralogy and Petrology, Vol 174, https://doi.org/ 10.1007/s00410-019-1552-z
Africa, South Africa
deposit - Roberts Victor, Jagersfontein
Abstract: Mantle eclogites are commonly accepted as evidence for ancient altered subducted oceanic crust preserved in the subcontinental lithospheric mantle (SCLM), yet the mechanism and extent of crustal recycling in the Archaean remains poorly constrained. In this study, we focus on the petrological and geochemical characteristics of 58 eclogite xenoliths from the Roberts Victor and Jagersfontein kimberlites, South Africa. Non-metasomatized samples preserved in the cratonic root have variable textures and comprise bimineralic (garnet (gt)-omphacite (cpx)), as well as kyanite (ky)- and corundum (cor)-bearing eclogites. The bimineralic samples were derived from a high-Mg variety, corresponding to depths of ~ 100-180 km, and a low-Mg variety corresponding to depths of ~ 180-250 km. The high-Al (ky-, cor-bearing) eclogites originated from the lowermost part of the cratonic root, and have the lowest REE abundances, and the most pronounced positive Eu and Sr anomalies. On the basis of the strong positive correlation between gt and cpx ?18O values (r2 = 0.98), we argue that ?18O values are unaffected by mantle processes or exhumation. The cpx and gt are in oxygen isotope equilibrium over a wide range in ?18O values (e.g., 1.1-7.6‰ in garnet) with a bi-modal distribution (peaks at ~ 3.6 and ~ 6.4‰) with respect to mantle garnet values (5.1 ± 0.3‰). Reconstructed whole-rock major and trace element compositions (e.g., MgO variation with respect to Mg#, Al2O3, LREE/HREE) of bimineralic eclogites are consistent with their protolith being oceanic crust that crystallized from a picritic liquid, marked by variable degrees of partial melt extraction. Kyanite and corundum-bearing eclogites, however, have compositions consistent with a gabbroic and pyroxene-dominated protolith, respectively. The wide range in reconstructed whole-rock ?18O values is consistent with a broadly picritic to pyroxene-rich cumulative sequence of depleted oceanic crust, which underwent hydrothermal alteration at variable temperatures. The range in ?18O values extends significantly lower than that of present-day oceanic crust and Cretaceous ophiolites, and this might be due to a combination of lower ?18O values of seawater in the Archaean or a higher temperature of seawater-oceanic crust interaction.
Contributions to Mineralogy and Petrology, Vol 174, https://doi.org/ 10.1007/s00410-019-1552-z
Africa, South Africa
deposit - Roberts Victor, Jagersfontein
Abstract: Mantle eclogites are commonly accepted as evidence for ancient altered subducted oceanic crust preserved in the subcontinental lithospheric mantle (SCLM), yet the mechanism and extent of crustal recycling in the Archaean remains poorly constrained. In this study, we focus on the petrological and geochemical characteristics of 58 eclogite xenoliths from the Roberts Victor and Jagersfontein kimberlites, South Africa. Non-metasomatized samples preserved in the cratonic root have variable textures and comprise bimineralic (garnet (gt)-omphacite (cpx)), as well as kyanite (ky)- and corundum (cor)-bearing eclogites. The bimineralic samples were derived from a high-Mg variety, corresponding to depths of ~ 100-180 km, and a low-Mg variety corresponding to depths of ~ 180-250 km. The high-Al (ky-, cor-bearing) eclogites originated from the lowermost part of the cratonic root, and have the lowest REE abundances, and the most pronounced positive Eu and Sr anomalies. On the basis of the strong positive correlation between gt and cpx ?18O values (r2 = 0.98), we argue that ?18O values are unaffected by mantle processes or exhumation. The cpx and gt are in oxygen isotope equilibrium over a wide range in ?18O values (e.g., 1.1-7.6‰ in garnet) with a bi-modal distribution (peaks at ~ 3.6 and ~ 6.4‰) with respect to mantle garnet values (5.1 ± 0.3‰). Reconstructed whole-rock major and trace element compositions (e.g., MgO variation with respect to Mg#, Al2O3, LREE/HREE) of bimineralic eclogites are consistent with their protolith being oceanic crust that crystallized from a picritic liquid, marked by variable degrees of partial melt extraction. Kyanite and corundum-bearing eclogites, however, have compositions consistent with a gabbroic and pyroxene-dominated protolith, respectively. The wide range in reconstructed whole-rock ?18O values is consistent with a broadly picritic to pyroxene-rich cumulative sequence of depleted oceanic crust, which underwent hydrothermal alteration at variable temperatures. The range in ?18O values extends significantly lower than that of present-day oceanic crust and Cretaceous ophiolites, and this might be due to a combination of lower ?18O values of seawater in the Archaean or a higher temperature of seawater-oceanic crust interaction.
Geochimica et Cosmochimica Acta, in press available 21p.
Africa, South Africa
deposit - Bultfontein
Abstract: Current understanding of the fate of subducted material (and related fluids) in the deep Earth can be improved by combining major and trace element geochemistry with stable isotopic compositions of mantle rocks or minerals. Limited isotopic fractionation during high temperature processes means that significant deviations from mantle-like isotope ratios in mantle rocks probably result from recycling of surficial material. To determine the effects and origins of mantle metasomatic fluids/melts, new ?15N and ?18O data have been collected for thirteen mantle xenoliths - harzburgites, wehrlites, lherzolites, and MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) rocks - from the Bultfontein kimberlite (Kimberley, South Africa), which show varying degrees of metasomatism. The ?18O values of olivine and orthopyroxene in phlogopite-free harzburgites match the mantle composition (?18Oolivine?=?+5.2?±?0.3‰; ?18Oorthopyroxene?=?+5.7?±?0.3‰; 2?s.d.), consistent with previous inferences that harzburgites were formed by interaction with ancient silica-rich melts unrelated to subduction processes. Wehrlite samples display mineral compositional characteristics (e.g., low La/Zr in clinopyroxene) resembling those of other products of kimberlite melt metasomatism, such as PIC (Phlogopite-Ilmenite-Clinopyroxene) rocks. The inferred interaction with kimberlite melts may be responsible for O isotopic disequilibrium between clinopyroxene and olivine (?18O?=?+0.2‰) in the wehrlites of this study. In contrast with broadly mantle-like ?18O values, the ?15N value of phlogopite in a wehrlite sample (+5.9‰) differs from the mantle composition (?15N?=??5?±?2‰). This unusual N isotopic composition in kimberlite-related mantle products might indicate that a recycled crustal component occurred in the source of the Kimberley kimberlites, or was assimilated during interaction with the lithospheric mantle. Similar major and trace element characteristics in clinopyroxene from phlogopite-lherzolite and MARID samples suggest metasomatism by fluids of similar composition. Lherzolite and MARID clinopyroxene ?18O values (as low as +4.4‰) extend below those reported in mantle peridotites (i.e. ?18Oclinopyroxene?=?+5.6?±?0.3‰; 2?s.d.), and strong negative correlations are found between mineral ?18O values and major element compositions (e.g., Na2O contents in clinopyroxene). Furthermore, phlogopite ?15N values (+4 to +7‰) in the studied lherzolite and MARID samples are higher than mantle values. Combined, the low ?18O-high ?15N isotopic signatures of MARID and lherzolite samples suggest progressive mantle metasomatism by a melt containing a recycled oceanic crust (eclogitic) component. This study demonstrates that progressive enrichment of the subcontinental lithospheric mantle may be inextricably linked to plate tectonics via recycling of subducted crustal material into the deep mantle.
The Southern African Institute of Mining and Metallurgy, Vol. 119, pp. 155-164.
Africa, Botswana
deposit - Jwaneng
Abstract: Despite the pre-eminence of the Jwaneng Diamond Mine as the world's richest diamond mine, the discovery story has long been clouded in mystery. This is the 45-year old untold story of the Jwaneng discovery and contemporaneous Bechuanaland/Botswana political and socioeconomic history.
European Journal of Mineralogy, Vol. 31, pp. 13-143.
Russia, Kola Peninsula
deposit - Khibiny
Abstract: The new mineral alexkhomyakovite K6(Ca2Na)(CO3)5Cl?6H2O (IMA2015-013) occurs in a peralkaline pegmatite at Mt. Koashva, Khibiny alkaline complex, Kola peninsula, Russia. It is a hydrothermal mineral associated with villiaumite, natrite, potassic feldspar, pectolite, sodalite, biotite, lamprophyllite, titanite, fluorapatite, wadeite, burbankite, rasvumite, djerfisherite, molybdenite and an incompletely characterized Na-Ca silicate. Alexkhomyakovite occurs as equant grains up to 0.2 mm, veinlets up to 3 cm long and up to 1 mm thick and fine-grained aggregates replacing delhayelite. Alexkhomyakovite is transparent to translucent, colourless, white or grey, with vitreous to greasy lustre. It is brittle, the Mohs hardness is ca. 3. No cleavage was observed, the fracture is uneven. D meas = 2.25(1), D calc = 2.196 g cm?3. Alexkhomyakovite is optically uniaxial (-), ? = 1.543(2), ? = 1.476(2). The infrared spectrum is reported. The chemical composition [wt%, electron microprobe data, CO2 and H2O contents calculated for 5 (CO3) and 6 (H2O) per formula unit (pfu), respectively] is: Na2O 4.09, K2O 35.72, CaO 14.92, MnO 0.01, FeO 0.02, SO3 0.11, Cl 4.32, CO2 28.28, H2O 13.90, -O=Cl -0.98, total 100.39. The empirical formula calculated on the basis of 9 metal cations pfu is K5.90Ca2.07Na1.03(CO3)5(SO4)0.01O0.05Cl0.95?6H2O. The numbers of CO3 groups and H2O molecules are based on structure data. Alexkhomyakovite is hexagonal, P63/mcm, a = 9.2691(2), c = 15.8419(4) Å, V = 1178.72(5) Å3 and Z = 2. The strongest reflections of the powder X-ray diffraction pattern [d Å(I)(hkl)] are: 7.96(27)(002), 3.486(35)(113), 3.011(100)(114), 2.977(32)(211), 2.676(36)(300), 2.626(42)(213, 115), 2.206(26)(311) and 1.982(17)(008). The crystal structure (solved from single-crystal X-ray diffraction data, R = 0.0578) is unique. It is based on (001) heteropolyhedral layers of pentagonal bipyramids (Ca,Na)O5(H2O)2 interconnected via carbonate groups of two types, edge-sharing ones and vertex-sharing ones. Ca and Na are disordered. Ten-fold coordinated K cations centre KO6Cl(H2O)3 polyhedra on either side of the heteropolyhedral layer. A third type of carbonate group and Cl occupy the interlayer. The mineral is named in honour of the outstanding Russian mineralogist Alexander Petrovich Khomyakov (1933-2012).
Abstract: The paper discusses the morphology and compositional variations of ilmenite group minerals from kimberlites of two phases at the Kimozero locality, the oldest in Russia. Phenocrysts of Mn-rich picroilmenite and Fe-rich geikielite in kimberlites of both phases are similar in morphology and composition. Ilmenite from cement in the second-phase kimberlites enriched in Mg and rimming small regularly shaped chrome spinel phenocrysts is not present in the first-phase kimberlites. Ilmenite, manganilmenite, and Fe-bearing pyrophanite (22-24 wt % MnO) abundant in the cement of the second-phase kimberlites are twice as rich in Nb and substantially richer in Mn than ilmenite up to manganilmenite from the cement of the first-phase kimberlites. Ilmenite and manganilmenite of the first-phase kimberlites is enriched in Zn (up to 1.5 wt % ZnO). Ilmenite from the second-phase kimberlites contains up to 3 wt % Cr2O3. In Nb concentration, kimberlitic rocks of the Kimozero are similar to those found in other parts of the world (up to 3.5 wt % Nb2O5). Significant Mn-enrichment of the ilmenite group minerals is a common feature of Kimozero kimberlitic rocks. It is suggested that kimberlites in which all ilmenite group minerals—from megacrysts and phenocrysts to small segregations in the cement—are enriched in Me, formed with the participation of carbonatite melts with increased alkalinity.
Abstract: The spatial and temporal association between lamprophyres and kimberlites provides unique opportunities to explore their genetic relationships. This paper explores such a relationship by detailing mineralogical and geochemical aspects of Korakkodu lamprophyre dykes located within the well?known Mesoproterozoic diamondiferous Wajrakarur Kimberlite field (WKF), towards the south?western margin of Paleo-Mesoproterozoic Cuddapah Basin, Eastern Dharwar Craton, southern India. Mineralogy reveals that these dykes belong to calc?alkaline variety of lamprophyres, but their geochemistry display mixed signals of both alkaline and calc?alkaline lamprophyres. These lamprophyres are highly potassic, and their high Al2O3 and low?TiO2 content implies a shoshonitic character. Low Mg#, Ni, and Cr concentration highlight their evolved nature. High (La/Yb)N and (Gd/Yb)N content is consistent with their derivation from low degrees of partial melting, whereas highly fractionated nature suggests the presence of garnet in their source. Absence of prominent Nb?Ta anomaly implies to the dilution of lithospheric mantle source by melts rich in HFSEs and low La/Nb ratio compared to those of the calc?alkaline island arc volcanics and suggests an asthenospheric overprint on lithospheric mantle source. Carbonatite metasomatism in the source region of these lamprophyres is apparent from conspicuously high?Zr/Hf ratio, and the HFSE budget of these lamprophyres are principally controlled by the presence of phlogopite veins in their lithospheric source. An extremely heterogeneous and layered lithospheric mantle beneath Eastern Dharwar Craton has been inferred from the divergent genetic history of Mesoproterozoic lamprophyres and kimberlites in the Wajrakarur field.
Abstract: Carbonatite-related rare-earth element (REE) deposits are the most important source of the world’s REE resources. Hydrothermal fluids have been proposed to play a significant role in the transport and precipitation of REEs, but fluid inclusion data on the hydrothermal processes in carbonatitic settings are relatively sparse. The Dalucao deposit, located in the Mianning-Dechang (MD) REE belt, Sichuan, China, is a Cenozoic carbonatite-related REE deposit (c. 12?Ma) that offers an excellent opportunity to investigate the evolution of ore-forming fluids. Brecciated and weathered ores are common in this deposit. The former are characterized by mineral assemblages comprising fluorite?+?barite?+?celestite?+?calcite?+?quartz?+?bastnäsite (No. 1 orebody) or fluorite?+?celestite?+?pyrite?+?muscovite?+?calcite?+?quartz?+?bastnäsite (No. 3 orebody), whereas the latter contain REE minerals, clay minerals, and minor gangue minerals. We present a comprehensive study of fluid inclusions from the Dalucao deposit to constrain its hydrothermal evolution. Magmatic, pegmatitic, hydrothermal, and supergene stages have been recognized. During the pegmatitic stage, the main minerals that formed were coarse-grained fluorite, barite, celestite, calcite, and quartz, which host melt inclusions, melt-fluid inclusions, and minor high-salinity fluid inclusions. The presence of melt and melt-fluid inclusions suggests a magmatic origin for the ore-forming fluids. Hydrothermal processes included at least two stages, characterized by hydrothermal veins that are developed in fractures within the carbonatite-syenite complex: (1) Fluid inclusions during the formation of the fluorite-quartz-barite veins in the pre-REE stage were trapped under immiscible conditions, as evidenced by the presence of CO2-bearing inclusions coexisting with aqueous ones. These immiscible CO2-bearing inclusions recorded a range of pressures from 1050 to 1600?bar. All of fluid inclusions in this stage exhibited homogenization temperatures varying from 278 to 442?°C, with salinities ranging from 3.2 to 45.1?wt% NaCl equivalent (equiv.). (2) The REE-stage fluids were represented by abundant aqueous inclusions, characterized by homogenization temperatures ranging from 147 to 323?°C and salinities between 1.1 and 9.5?wt% NaCl equiv. These data suggest that the ore-forming fluids forming the Dalucao deposit evolved from high-temperature, high-pressure, high-salinity, CO2-rich to low-temperature, low-pressure, low-salinity, CO2-poor. Gas- and ion-chromatographic analyses combined with mineralogical features indicate that the initial fluids were rich in REEs, (SO4)2?, Cl?, F?, Na+, K+, Ca2+, and volatile components (e.g., H2O, CO2, N2, CH4, Ar, and C2H6). H-O isotope analyses of quartz suggest that the hydrothermal fluids had a dominantly magmatic signature and were gradually diluted by meteoric waters. Hydrothermal REE transport was probably controlled by F?, (SO4)2?, and Cl? as complexing ligands. We propose that fluid cooling and mixing rather than immiscibility led to the precipitation of bastnäsite during the waning stage of hydrothermal activity. Taken together, the inclusion data and observations of alteration, paragenesis and mineralization have provided insights into the development of REE mineralization and the further exploration of carbonatite-related REE resources.
Journal of Volacnology and Geothermal Research, Vol. 373, pp. 68-96.
Australia, South Australia
deposit - Eurelia
Abstract: Kimberlites of Jurassic age occur in various parts of South Australia. Thirty-nine of these kimberlites, which are mostly new discoveries, were studied to characterize their structural setting, their petrography, and the composition of their constituent minerals. Although some of the kimberlites in South Australia occur on the Archean to Paleoproterozoic Gawler Block, most are part of a northwest-trending, semi-continuous kimberlite dike swarm located in the Adelaide Fold Belt. The kimberlites typically occur as dikes or sills, but diatremes are also present. In the Adelaide Fold Belt, diatremes are restricted to the hinge zones of regional-scale folds within thick sedimentary sequences of the Adelaidean Supergroup. Despite widespread and severe alteration, coherent and pyroclastic kimberlites can be readily distinguished. U-Pb and Sr/Nd isotopic compositions of groundmass perovskite indicate that all kimberlites belong to the same age group (177-197?Ma) and formed in a near-primitive mantle environment (87Sr/86Sr: 0.7038-0.7052, ?Nd: ?0.07 to +2.97). However, the kimberlites in South Australia are compositionally diverse, and range from olivine-dominated varieties (macrocrystic kimberlites) to olivine-poor, phlogopite-dominated varieties (micaceous kimberlites). Macrocrystic kimberlites contain magnesium-rich groundmass phlogopite and spinel, and they are typically olivine macrocryst-rich. Micaceous kimberlites, in contrast, contain more iron- and titanium-rich groundmass phlogopite and less magnesian spinel, and olivine macrocrysts are rare or absent. Correlations between phlogopite and spinel compositions with modal abundances of olivine, indicate that the contrast between macrocrystic and micaceous kimberlites is primarily linked to the amount of mantle components that were incorporated into a compositionally uniform parental mafic silicate melt. We propose that assimilation of xenocrystic magnesite and incorporation of xenocrystic olivine from dunitic source rocks were the key processes that modified the parental silicate melt and created the unique hybrid (carbonate-silicate) character of kimberlites. Based on the composition of xenoliths and xenocrysts, the lithospheric mantle sampled by the South Australian kimberlites is relatively uniform, and extends to depths of 160-170?km, which is slightly below the diamond stability field. Only beneath the Eurelia area does the lithosphere appear thicker (>175?km), which is consistent with the presence of diamonds in some of the Eurelia kimberlites.
Abstract: Porphyritic olivine kimberlitic breccia, discovered in the Dörbed Banner of Inner Mongolia, Western China, is referred to as Longtou Shan Kimberlite in our study. This kimberlite occurs as a pipe in the Halahuogete Formation of Bayan Obo Group. Zircon U-Pb ages of Longtou Shan Kimberlite reveals a Mesoproterozoic age of ~1,552 Ma, constraining the deposition age of Halahuogete Formation to the Mesoproterozoic. Compared with Mesoproterozoic kimberlite of the ancient landmass, it can be inferred that the North China Craton is a member of the Ur ancient continent of the Columbia supercontinent. Furthermore, according to the tectonic background of the Bayan Obo Group, we raise this possibility that “Bayan Obo Aulacogen” should be renamed the “Bayan Obo Continental Rift.”
Abstract: Megacrysts are large (cm to >20?cm in size) mantle-derived crystals, which are commonly entrained by kimberlite magmas, comprising of olivine, orthopyroxene, clinopyroxene, phlogopite, garnet, ilmenite and zircon as common phases. Numerous studies have shown megacrysts to contain polymineralic inclusions, which have been interpreted to represent entrapped kimberlite melt. To constrain the origin of these inclusions in megacrysts and their relationship to kimberlite magmatism, we present a detailed petrographic and geochemical study of clinopyroxene and olivine megacrysts and their hosted inclusions from the Diavik, Jericho, Leslie (Slave Craton, Canada) and Udachnaya-East (Siberian Craton, Russia) kimberlites. The studied megacrysts are between 1 and 3?cm in size and representative of both the Cr-rich and Cr-poor suites. Megacrysts contain two types of inclusions: i. Large (<0.5-5?mm in size) round-to-irregular shaped polymineralic inclusions, which are composed of minerals similar to the host kimberlite groundmass, and consist of olivine, calcite, spinel, perovskite, phlogopite and apatite (± serpentine, alkali-carbonates, alkali-chlorides, barite). ii. Swarms/trails of ‘micro melt inclusions’ (MMI; <1-5??m in size), which surround polymineralic inclusions, veins and fractures, thereby forming a ‘spongy’ texture. MMIs generally contain multiphase assemblages similar to polymineralic inclusions as well as various additional phases, such as alkali-carbonates or alkali-chlorides, which are typically absent in polymineralic inclusions and the surrounding kimberlite groundmass. Textural and geochemical evidence suggests that polymineralic inclusions in megacrysts crystallised from kimberlite melt, which infiltrated along fracture/vein networks. The polymineralic inclusion assemblages resulted from disequilibria reactions between the host megacryst and infiltrating kimberlite melt, which was likely enhanced by rapidly changing conditions during magmatic ascent. The connectivity of polymineralic inclusions to the kimberlite groundmass via network veins/fractures suggests that they are susceptible to infiltrating post-emplacement fluids. Therefore, the vast majority of polymineralic inclusions are unlikely to represent ‘pristine’ entrapped kimberlite melt. In contrast, MMIs are isolated within megacrysts (i.e. not connected to fractures/veins and therefore shielded from post-magmatic fluids) and probably represent entrapped remnants of the variably differentiated kimberlite melt, which was more enriched in alkalis-Cl-S-CO2 than serpentinised polymineralic inclusions and the host rocks exposed at Earth's surface as kimberlites.
Abstract: Megacrysts are large (cm to >20?cm in size) mantle-derived crystals, which are commonly entrained by kimberlite magmas, comprising of olivine, orthopyroxene, clinopyroxene, phlogopite, garnet, ilmenite and zircon as common phases. Numerous studies have shown megacrysts to contain polymineralic inclusions, which have been interpreted to represent entrapped kimberlite melt. To constrain the origin of these inclusions in megacrysts and their relationship to kimberlite magmatism, we present a detailed petrographic and geochemical study of clinopyroxene and olivine megacrysts and their hosted inclusions from the Diavik, Jericho, Leslie (Slave Craton, Canada) and Udachnaya-East (Siberian Craton, Russia) kimberlites. The studied megacrysts are between 1 and 3?cm in size and representative of both the Cr-rich and Cr-poor suites. Megacrysts contain two types of inclusions: i. Large (<0.5-5?mm in size) round-to-irregular shaped polymineralic inclusions, which are composed of minerals similar to the host kimberlite groundmass, and consist of olivine, calcite, spinel, perovskite, phlogopite and apatite (± serpentine, alkali-carbonates, alkali-chlorides, barite). ii. Swarms/trails of ‘micro melt inclusions’ (MMI; <1-5??m in size), which surround polymineralic inclusions, veins and fractures, thereby forming a ‘spongy’ texture. MMIs generally contain multiphase assemblages similar to polymineralic inclusions as well as various additional phases, such as alkali-carbonates or alkali-chlorides, which are typically absent in polymineralic inclusions and the surrounding kimberlite groundmass. Textural and geochemical evidence suggests that polymineralic inclusions in megacrysts crystallised from kimberlite melt, which infiltrated along fracture/vein networks. The polymineralic inclusion assemblages resulted from disequilibria reactions between the host megacryst and infiltrating kimberlite melt, which was likely enhanced by rapidly changing conditions during magmatic ascent. The connectivity of polymineralic inclusions to the kimberlite groundmass via network veins/fractures suggests that they are susceptible to infiltrating post-emplacement fluids. Therefore, the vast majority of polymineralic inclusions are unlikely to represent ‘pristine’ entrapped kimberlite melt. In contrast, MMIs are isolated within megacrysts (i.e. not connected to fractures/veins and therefore shielded from post-magmatic fluids) and probably represent entrapped remnants of the variably differentiated kimberlite melt, which was more enriched in alkalis-Cl-S-CO2 than serpentinised polymineralic inclusions and the host rocks exposed at Earth's surface as kimberlites.
Abstract: Megacrysts are large (cm to >20?cm in size) mantle-derived crystals, which are commonly entrained by kimberlite magmas, comprising of olivine, orthopyroxene, clinopyroxene, phlogopite, garnet, ilmenite and zircon as common phases. Numerous studies have shown megacrysts to contain polymineralic inclusions, which have been interpreted to represent entrapped kimberlite melt. To constrain the origin of these inclusions in megacrysts and their relationship to kimberlite magmatism, we present a detailed petrographic and geochemical study of clinopyroxene and olivine megacrysts and their hosted inclusions from the Diavik, Jericho, Leslie (Slave Craton, Canada) and Udachnaya-East (Siberian Craton, Russia) kimberlites. The studied megacrysts are between 1 and 3?cm in size and representative of both the Cr-rich and Cr-poor suites. Megacrysts contain two types of inclusions: i. Large (<0.5-5?mm in size) round-to-irregular shaped polymineralic inclusions, which are composed of minerals similar to the host kimberlite groundmass, and consist of olivine, calcite, spinel, perovskite, phlogopite and apatite (± serpentine, alkali-carbonates, alkali-chlorides, barite). ii. Swarms/trails of ‘micro melt inclusions’ (MMI; <1-5??m in size), which surround polymineralic inclusions, veins and fractures, thereby forming a ‘spongy’ texture. MMIs generally contain multiphase assemblages similar to polymineralic inclusions as well as various additional phases, such as alkali-carbonates or alkali-chlorides, which are typically absent in polymineralic inclusions and the surrounding kimberlite groundmass. Textural and geochemical evidence suggests that polymineralic inclusions in megacrysts crystallised from kimberlite melt, which infiltrated along fracture/vein networks. The polymineralic inclusion assemblages resulted from disequilibria reactions between the host megacryst and infiltrating kimberlite melt, which was likely enhanced by rapidly changing conditions during magmatic ascent. The connectivity of polymineralic inclusions to the kimberlite groundmass via network veins/fractures suggests that they are susceptible to infiltrating post-emplacement fluids. Therefore, the vast majority of polymineralic inclusions are unlikely to represent ‘pristine’ entrapped kimberlite melt. In contrast, MMIs are isolated within megacrysts (i.e. not connected to fractures/veins and therefore shielded from post-magmatic fluids) and probably represent entrapped remnants of the variably differentiated kimberlite melt, which was more enriched in alkalis-Cl-S-CO2 than serpentinised polymineralic inclusions and the host rocks exposed at Earth's surface as kimberlites.
Abstract: Megacrysts are large (cm to >20?cm in size) mantle-derived crystals, which are commonly entrained by kimberlite magmas, comprising of olivine, orthopyroxene, clinopyroxene, phlogopite, garnet, ilmenite and zircon as common phases. Numerous studies have shown megacrysts to contain polymineralic inclusions, which have been interpreted to represent entrapped kimberlite melt. To constrain the origin of these inclusions in megacrysts and their relationship to kimberlite magmatism, we present a detailed petrographic and geochemical study of clinopyroxene and olivine megacrysts and their hosted inclusions from the Diavik, Jericho, Leslie (Slave Craton, Canada) and Udachnaya-East (Siberian Craton, Russia) kimberlites. The studied megacrysts are between 1 and 3?cm in size and representative of both the Cr-rich and Cr-poor suites. Megacrysts contain two types of inclusions: i. Large (<0.5-5?mm in size) round-to-irregular shaped polymineralic inclusions, which are composed of minerals similar to the host kimberlite groundmass, and consist of olivine, calcite, spinel, perovskite, phlogopite and apatite (± serpentine, alkali-carbonates, alkali-chlorides, barite). ii. Swarms/trails of ‘micro melt inclusions’ (MMI; <1-5??m in size), which surround polymineralic inclusions, veins and fractures, thereby forming a ‘spongy’ texture. MMIs generally contain multiphase assemblages similar to polymineralic inclusions as well as various additional phases, such as alkali-carbonates or alkali-chlorides, which are typically absent in polymineralic inclusions and the surrounding kimberlite groundmass. Textural and geochemical evidence suggests that polymineralic inclusions in megacrysts crystallised from kimberlite melt, which infiltrated along fracture/vein networks. The polymineralic inclusion assemblages resulted from disequilibria reactions between the host megacryst and infiltrating kimberlite melt, which was likely enhanced by rapidly changing conditions during magmatic ascent. The connectivity of polymineralic inclusions to the kimberlite groundmass via network veins/fractures suggests that they are susceptible to infiltrating post-emplacement fluids. Therefore, the vast majority of polymineralic inclusions are unlikely to represent ‘pristine’ entrapped kimberlite melt. In contrast, MMIs are isolated within megacrysts (i.e. not connected to fractures/veins and therefore shielded from post-magmatic fluids) and probably represent entrapped remnants of the variably differentiated kimberlite melt, which was more enriched in alkalis-Cl-S-CO2 than serpentinised polymineralic inclusions and the host rocks exposed at Earth's surface as kimberlites.
Chemical Geology, doi.org/10,1016/j.chem geo.2019.04.014 37p.
Africa, Sierra Leone
deposit - Zimmi
Abstract: Here we present SIMS data for a suite of Zimmi sulphide-bearing diamonds that allow us to evaluate the origin and redox-controlled speciation of diamond-forming fluids for these Neoproterozoic eclogitic diamonds. Low ?13C values below ?15‰ in three diamonds result from fluids that originated as carbon in the oceanic crust, and was recycled into the diamond-stable subcratonic lithospheric mantle beneath Zimmi during subduction. ?13C values between ?6.7 and ?8.3‰ in two diamonds are within the range for mantle-derived carbon and could reflect input from mantle fluids, serpentinised peridotite, or homogenised abiogenic and/or biogenic carbon (low ?13C values) and carbonates (high ?13C values) in the oceanic crust. Diamond formation processes in eclogitic assemblages are not well constrained and could occur through redox exchange reactions with the host rock, cooling/depressurisation of CHO fluids or during H2O-loss from CHO fluids. In one Zimmi diamond studied here, a core to rim trend of decreasing ?13C (?23.4 to ?24.5‰) and decreasing [N] is indicative of formation from reduced CH4-bearing fluids. Unlike mixed CH4-CO2 fluids near the water maximum, isochemical diamond precipitation from such reduced CHO fluids will only occur during depressurisation (ascent) and should not produce coherent fractionation trends in single diamonds that reside at constant depth (pressure). Furthermore, due to a low relative proportion of the total carbon in the fluid being precipitated, measurable carbon isotopic variations in diamond are not predicted in this model and therefore cannot be reconciled with the 1‰ internal core-to- rim variation. Consequently, this Zimmi eclogitic diamond showing a coherent trend in ?13C and [N] likely formed through oxidation of methane by the host eclogite, although the mineralogical evidence for this process is currently lacking.
Fulop, A., Kopylova, M., Kurszlaukis, S., Hilchie, L., Ellemers, P.
A reply to the comment by Germon et al. on the Petrography of the Snap Lake kimberlite dyke ( Northwest Territories, Canada) and its interaction with country rock granitoids.
Geochimica et Cosmochimica Acta, in press available, 19p.
Africa, South Africa, Canada, South America, Brazil
deposit - Lac de Gras, Paranaiba
Abstract: Kimberlites are the deepest melts produced on Earth that are erupted at the surface and can therefore provide unique insights into the composition and evolution of the mantle. Radiogenic isotopes provide ambiguous evidence for the occurrence of recycled crustal material in kimberlite sources. Oxygen isotopes can fractionate significantly only in the shallow crust, and thus represent a powerful tracer of subducted material in the sources of kimberlite. To constrain the oxygen isotope composition of kimberlite melts, we have examined olivine grains in eleven Cretaceous to Eocene archetypal kimberlites from southern Africa, Lac de Gras (Canada) and Alto Paranaiba (Brazil), which exhibit radiogenic isotope evidence for recycled crustal material in their sources including highly radiogenic Pb isotopes and Nd-Hf isotope compositions deviating below the mantle array. Olivine grains are commonly zoned between a mantle-derived xenocrystic core and one or more magmatic overgrowths, i.e. occasional internal zones, ubiquitous rims and rare rinds (moving outward from the core). The oxygen isotope composition of different olivine zones was determined in situ within separated olivine grains by secondary ion mass spectrometry (SIMS) after point selection using back-scattered electron (BSE) images combined with major and minor element analyses. With the exception of a few cores, the ?18O values of different olivine zones do not deviate from typical mantle olivine values of 5.18?±?0.28‰ (Mattey et al., 1994). There are no correlations between oxygen isotopes and major/minor element compositions for internal zones and rims from individual localities or in the entire dataset. This indicates that the oxygen isotope composition of kimberlite melts is not affected by melt differentiation to the point of olivine rim crystallisation. However, olivine rinds from the Koala kimberlite (Canada) display an inverse correlation between ?18O and Mn-Ca concentrations, with ?18O values extending below the mantle range, which is probably due to carbonate fractionation, CO2 degassing and/or assimilation of serpentine-rich material after kimberlite emplacement in the upper crust. The mantle-like ?18O composition of olivine internal zones and rims suggests that assimilation of mantle material and liberation of a CO2-rich phase during ascent in the mantle do not significantly modify the original ?18O signature of kimberlite melts. Modelling of oxygen isotope fractionation shows that up to 15 wt% of CO2 can be lost by kimberlites en route to the upper crust. Our results combined with mass balance calculations indicate that only a limited amount (<5-10 wt%) of recycled crustal material could occur in the source of kimberlites from southern Africa, Lac de Gras and Alto Paranaiba, or that the recycled material had an oxygen isotope composition similar to the mantle.
Geochimica et Cosmochimica Acta, in press available, 19p.
Africa, South Africa, Canada, South America, Brazil
deposit - Lac de Gras, Paranaiba
Abstract: Kimberlites are the deepest melts produced on Earth that are erupted at the surface and can therefore provide unique insights into the composition and evolution of the mantle. Radiogenic isotopes provide ambiguous evidence for the occurrence of recycled crustal material in kimberlite sources. Oxygen isotopes can fractionate significantly only in the shallow crust, and thus represent a powerful tracer of subducted material in the sources of kimberlite. To constrain the oxygen isotope composition of kimberlite melts, we have examined olivine grains in eleven Cretaceous to Eocene archetypal kimberlites from southern Africa, Lac de Gras (Canada) and Alto Paranaiba (Brazil), which exhibit radiogenic isotope evidence for recycled crustal material in their sources including highly radiogenic Pb isotopes and Nd-Hf isotope compositions deviating below the mantle array. Olivine grains are commonly zoned between a mantle-derived xenocrystic core and one or more magmatic overgrowths, i.e. occasional internal zones, ubiquitous rims and rare rinds (moving outward from the core). The oxygen isotope composition of different olivine zones was determined in situ within separated olivine grains by secondary ion mass spectrometry (SIMS) after point selection using back-scattered electron (BSE) images combined with major and minor element analyses. With the exception of a few cores, the ?18O values of different olivine zones do not deviate from typical mantle olivine values of 5.18?±?0.28‰ (Mattey et al., 1994). There are no correlations between oxygen isotopes and major/minor element compositions for internal zones and rims from individual localities or in the entire dataset. This indicates that the oxygen isotope composition of kimberlite melts is not affected by melt differentiation to the point of olivine rim crystallisation. However, olivine rinds from the Koala kimberlite (Canada) display an inverse correlation between ?18O and Mn-Ca concentrations, with ?18O values extending below the mantle range, which is probably due to carbonate fractionation, CO2 degassing and/or assimilation of serpentine-rich material after kimberlite emplacement in the upper crust. The mantle-like ?18O composition of olivine internal zones and rims suggests that assimilation of mantle material and liberation of a CO2-rich phase during ascent in the mantle do not significantly modify the original ?18O signature of kimberlite melts. Modelling of oxygen isotope fractionation shows that up to 15 wt% of CO2 can be lost by kimberlites en route to the upper crust. Our results combined with mass balance calculations indicate that only a limited amount (<5-10 wt%) of recycled crustal material could occur in the source of kimberlites from southern Africa, Lac de Gras and Alto Paranaiba, or that the recycled material had an oxygen isotope composition similar to the mantle.
Abstract: Identification of the primary compositions of mantle-derived melts is crucial for understanding mantle compositions and physical conditions of mantle melting. However, these melts rarely reach the Earth's surface unmodified because of contamination, crystal fractionation and degassing, processes that occur almost ubiquitously after melt generation. Here we report snapshots of the melts preserved in sheared peridotite xenoliths from the Udachnaya-East kimberlite pipe, in the central part of the Siberian craton. These xenoliths are among the deepest mantle samples and were delivered by kimberlite magma from 180-230?km depth interval, i.e. from the base of the cratonic lithosphere. The olivine grains of the sheared peridotites contain secondary inclusions of the crystallized melt with bulk molar (Na?+?K)/Ca?~?3.4. Various Na-K-Ca-, Na-Ca-, Na-Mg-, Ca-Mg- and Ca-carbonates, Na-Mg-carbonates with additional anions, alkali sulphates and halides are predominant among the daughter minerals in secondary melt inclusions, whereas silicates, oxides, sulphides and phosphates are subordinate. These inclusions can be considered as Cl-S-bearing alkali-carbonate melts. The presence of aragonite, a high-pressure polymorph of CaCO3, among the daughter minerals suggests a mantle origin for these melt inclusions. The secondary melt inclusions in olivine from the sheared peridotite xenoliths and the melt inclusions in phenocrystic olivines from the host kimberlites demonstrate similarities, in daughter minerals assemblages and trace-element compositions. Moreover, alkali-rich minerals (carbonates, halides, sulphates and sulphides) identified in the studied melt inclusions are also present in the groundmass of the host kimberlites. These data suggests a genetic link between melt enclosed in olivine from the sheared peridotites and melt parental to the Udachnaya-East kimberlites. We suggest that the melt inclusions in olivine from mantle xenoliths may represent near primary, kimberlite melts. These results are new evidence in support of the alkali?carbonate composition of kimberlite melts in their source regions, prior to the kimberlite emplacement into the crust, and are in stark contrast to the generally accepted ultramafic silicate nature of parental kimberlite liquids.
Geochimica et Cosmochimica Acta, in press available, 16p.
Africa, South Africa
deposit - Kimberly region
Abstract: Carbonate-bearing assemblages in the mantle have been interpreted to be the source for Si-undersaturated, CO2-rich magmas, including kimberlites. However, direct evidence for carbonate in the mantle is rare in the contemporary literature. Here we present petrography, trace element, and C-O-Sr-Nd-Pb isotope composition for a suite of carbonate xenoliths from the Kimberley region kimberlites to ascertain their mantle or crustal origin and gain insight to the potential for the occurrence of carbonate in the mantle. Carbonate xenoliths were found in large kimberlite blocks from the Bultfontein kimberlite and Big Hole region. The xenoliths are characterised by pale green alteration margins made of fine-grained microlites of an unknown mineral as well as spherules surrounded by glassy material. They are generally 1–4?cm in size, coarse-grained (1–2?mm), and comprised entirely of calcite. Carbonate xenoliths from the Bultfontein kimberlite have low total REE concentrations (0.2–4.9?ppm), constant 87Sr/86Sri (0.7047–0.7049) combined with variable ?Ndi (?0.1 to ?26.2) and 206Pb/204Pbi, 207Pb/204Pbi, and 208Pb/204Pbi of 16.7–18.8, 15.3–15.6, 36.5–38.4, respectively. Xenoliths from the Big Hole sample have higher 87Sr/86Sri (0.7088–0.7095), lower ?Ndi (?24.5 to ?3.8), and 206Pb/204Pbi, 207Pb/204Pbi, and 208Pb/204Pbi of 18.9–19.9, 15.7–15.8, 38.4–38.8, respectively. The ?13C values for both Bultfontein (?5.7 to ?6.6‰) and Big Hole (?4.7 to ?5.4‰) carbonates are within the typical range expected for mantle-derived carbonate. The ?18O values (15.5–17.5‰) are higher than those of mantle silicate rocks, indicative of late-stage low-temperature interaction with fluids; a common feature of groundmass calcite in the Kimberley kimberlites. The Sr- and C- isotope composition of the Bultfontein xenoliths indicates a mantle origin whereas the Big Hole xenolith Sr- and C-isotopes are more ambiguous. Isotope mixing models are inconsistent with interaction between the host kimberlite and carbonate xenoliths. Correlation between ?Ndi and ?18O values for the Bultfontein xenoliths indicates late-stage interaction with low-temperature fluids, which may also be responsible for the large range in ?Ndi. This in turn indicates that the highest ?Ndi of ?0.1 represents the primary carbonate xenolith signature, and this value overlaps typical Group I kimberlites. We discuss two possible origins for the carbonate xenoliths. (1) Carbonate xenoliths from the sub-continental lithospheric mantle (SCLM), where quenched margins and the large range of ?Ndi are related to formation in the mantle. (2) Carbonate xenoliths from an earlier phase of carbonatite magmatism. The similarity of isotope signatures of the Bultfontein carbonates to Group I kimberlite may further suggest a link between kimberlite and carbonatite volcanism such as observed elsewhere in the world.
Contributions to Mineralogy and Petrology, Vol. 174, p. 29- 13p.
Russia, Siberia
deposit - Udachnaya
Abstract: We have studied by X-ray diffractometry the crystallographic orientation relationships (CORs) between magnesiochromite (mchr) inclusions and their diamond hosts in gem-quality stones from the mines Udachnaya (Siberian Russia), Damtshaa (Botswana) and Panda (Canada); in total 36 inclusions in 23 diamonds. In nearly half of the cases (n?=?17), [111]mchr is parallel within error to [111]diamond, but the angular misorientation for other crystallographic directions is generally significant. This relationship can be described as a case of rotational statistical COR, in which inclusion and host share a single axis (1 df). The remaining mchr-diamond pairs (n?=?19) have a random COR (2 df). The presence of a rotational statistical COR indicates that the inclusions have physically interacted with the diamond before their final incorporation. Of all possible physical processes that may have influenced mchr orientation, those driven by surface interactions are not considered likely because of the presence of fluid films around the inclusions. Mechanical interaction between euhedral crystals in a fluid-rich environment is therefore proposed as the most likely mechanism to produce the observed rotational COR. In this scenario, neither a rotational nor a random COR can provide information on the relative timing of growth of mchr and diamond. Some multiple, iso-oriented inclusions within single diamonds, however, indicate that mchr was partially dissolved during diamond growth, suggesting a protogenetic origin of these inclusions.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0588-5 17p.
Africa, South Africa
deposit - De Beers dyke
Abstract: We present petrographic and mineral chemical data for a suite of samples derived from the De Beers dyke, a contemporaneous, composite intrusion bordering the De Beers pipe (Kimberley, South Africa). Petrographic features and mineral compositions indicate the following stages in the evolution of this dyke: (1) production of antecrystic material by kimberlite-related metasomatism in the mantle (i.e., high Cr-Ti phlogopite); (2) entrainment of wall-rock material during ascent through the lithospheric mantle, including antecrysts; (3) early magmatic crystallisation of olivine (internal zones and subsequently rims), Cr-rich spinel, rutile, and magnesian ilmenite, probably on ascent to the surface; and (4) crystallisation of groundmass phases (i.e., olivine rinds, Fe-Ti-rich spinels, perovskite, apatite, monticellite, calcite micro-phenocrysts, kinoshitalite-phlogopite, barite, and baddeleyite) and the mesostasis (calcite, dolomite, and serpentine) on emplacement in the upper crust. Groundmass and mesostasis crystallisation likely forms a continuous sequence with deuteric/hydrothermal modification. The petrographic features, mineralogy, and mineral compositions of different units within the De Beers dyke are indistinguishable from one another, indicating a common petrogenesis. The compositions of antecrysts (i.e., high Cr-Ti phlogopite) and magmatic phases (e.g., olivine rims, magnesian ilmenite, and spinel) overlap those from the root zone intrusions of the main Kimberley pipes (i.e., Wesselton, De Beers, Bultfontein). However, the composition of these magmatic phases is distinct from those in ‘evolved’ intrusions of the Kimberley cluster (e.g., Benfontein, Wesselton water tunnel sills). Although the effects of syn-emplacement flow processes are evident (e.g., alignment of phases parallel to contacts), there is no evidence that the De Beers dyke has undergone significant pre-emplacement crystal fractionation (e.g., olivine, spinel, ilmenite). This study demonstrates the requirement for detailed petrographic and mineral chemical studies to assess whether individual intrusions are in fact ‘evolved’; and that dykes are not necessarily produced by differentiated magmas.
Abstract: Six diamonds with a fibrous core, intermediate zone and monocrystalline outer zone (“cloudy diamonds”) from the Koffiefontein mine, South Africa, were investigated for N concentrations, carbon isotope compositions and micro-inclusion compositions along core to rim traverses. This study evaluates the nature of the change from fibrous to gem diamond growth and the relation between major element composition of high density fluid inclusions and N ? ?¹³C in fibrous growth zones. Three diamonds contain saline to carbonatitic fluid micro-inclusions with constant or increasing carbon isotope values which are inferred to have formed by varying amounts of Rayleigh fractionation in a closed system of a carbonate-bearing fluid. Continuous N ? ?¹³C fractionation trends from the fibrous to gem growth zone in two of the diamonds and equally low nitrogen aggregation states indicate formation of diamond shortly before kimberlite eruption from a single fluid without a time gap between fibrous and gem diamond growth. High major element/CO32- ratios in the growth media resulted in a constant major element composition of the fluid inclusions found in the studied fibrous diamonds. The transition from fibrous to gem diamond growth is likely caused by the precipitation of diamond reducing the degree of oversaturation of carbon in the fluid and hence decreasing the rate of diamond growth. Two other diamonds have inclusions that change from silicate minerals in the inner fibrous growth zones towards pure saline fluid compositions in the outer fibrous growth zones. This decrease in Si, Mg and Ca and increase in K and Cl in the inclusions is accompanied by a decrease in ?¹³C values and N contents. These trends are suggested to be the result from gradually mixing in more saline fluids with lower ?¹³C values. One diamond with silicic inclusions has significant N aggregation into B-centres, suggesting this fluid is different and that diamond formation occurred significantly (e.g. 1250 °C gives ?10 Ma) before the kimberlite eruption.
Abstract: Bimineralic eclogites and pyroxenites (n?=?75?±?accessory rutile, ilmenite, sulphide, apatite) from the Koidu kimberlite (West African Craton) were investigated for mineral major and trace elements and mineral Sr-Nd isotope compositions to constrain (1) the nature and age of their basaltic to picritic protoliths, and (2) the effect, timing and source of mantle metasomatism. Consistent with published work, samples are grouped into low-Mg eclogites with Mg# from 0•49 to 0•73 (median 0•59; n?=?40) and high-Mg eclogites with Mg# from 0•60 to 0•88 (median 0•75; n?=?14), plus pyroxenites [clinopyroxene Na/(Na + Ca) <0•2; n?=?8] and gabbroic eclogites and pyroxenite (Eu/Eu* of reconstructed bulk-rocks >1•05; n?=?8), with five unclassifiable samples. Reconstructed low-Mg and gabbroic eclogites have major and trace element systematics (Eu/Eu*-heavy rare earth elements-Y) indicating crustal protolith crystallisation, confirming an origin as subducted oceanic crust. Their high FeO contents at MgO >?10?wt % require an Fe-rich source, the high melt productivity of which led to the formation of thicker crust, perhaps in a plateau-like setting. This is consistent with SiO2-MgO relationships indicating differentiation at ?0•5?GPa. Unradiogenic Sr in some clinopyroxene (87Sr/86Sr of 0•7010-0•7015), combined with light rare earth element (LREE) depletion relative to normal mid-ocean ridge basalt (N-MORB) for the majority of samples (average N-MORB-normalised Nd/Yb of unmetasomatised samples = 0•51), suggests eclogitisation and partial melt loss in the Neoarchaean, possibly coeval with and parental to 2•7?Ga overlying continental crust. Most reconstructed high-Mg eclogites and some pyroxenites formed by metasomatic overprinting of low-Mg eclogites and gabbroic eclogites, as indicated by the preservation of positive Eu anomalies in some samples, and by the Mg-poorer composition of included versus matrix minerals. Coupled enrichment in MgO, SiO2 and Cr2O3 and in incompatible elements (Sr, LREE, Pb, Th and U) is ascribed to metasomatism by a kimberlite-like, small-volume, carbonated ultramafic melt, mediated by addition of clinopyroxene from the melt (i.e. stealth metasomatism). Strontium-Nd isotope systematics suggest a Neoproterozoic age for this metasomatic event, possibly linked to Rodinia break-up, which facilitated intrusion of asthenospheric carbonated melts with an ocean island basalt-like 87Sr/86Sri of ?0•7035. Cretaceous kimberlite magmatism (including Koidu), with more radiogenic 87Sr/86Sr (?0•7065, intermediate between Kaapvaal kimberlites and orangeites), may have been partially sourced from associated Neoproterozoic metasomes. The presence of diamonds in low-Mg eclogites, but absence in high-Mg eclogites, indicates the diamond-destructive nature of this event. Nevertheless, the moderate proportion of affected eclogites (?35%) suggests preservation of a sizeable diamond-friendly mantle eclogite reservoir beneath Koidu.
Abstract: Megacrysts are mineral grains of garnet, clinopyroxene, orthopyroxene, ilmenite, olivine, phlogopite and zircon larger than 10 mm frequently observed in kimberlite occurrences across the world, with reported sizes commonly exceeding 10 cm. Despite their common occurrence and decades of research into their origin, megacryst petrogenesis is still a debated topic amongst petrologists. A strictly phenocrystal origin is doubted, with recent research suggesting a multi-stage model involving isobaric formation over a wide temperature range, followed by metasomatism of a protokimberlite fluid that replaces mantle minerals. Our project aims to contribute to ongoing research by modeling the metasomatism of the ambient peridotitic mantle affected by the fluid using major and trace element data obtained from megacrysts from the Jurassic Muskox kimberlite pipe of the Slave province of Canada. We report major element compositions of 24 megacryst samples of garnet, olivine, clinopyroxene and ilmenite and employ DEW (Deep Earth Water) modelling to establish the composition of the potential metasomatizing agent and mineral trends that result from the mantle metasomatism. This project has important implications for not only constraining the composition of the source fluids, but also understanding the reactions in the cratonic mantle leading to the kimberlite melt formation.
Abstract: The ca. 1153?Ma Premier kimberlite pipe on the Kaapvaal craton has been intruded by late-stage kimberlite and carbonatite magmas forming discrete 0.5 to 5?m wide dykes within the lower diatreme. On the basis of petrography and geochemistry, the fresh kimberlite dykes represent archetypal monticellite phlogopite kimberlite of Group-1 affinity. Their mineral compositions, however, show marked deviations from trends that are typically considered as diagnostic for Group-1 kimberlite in mineralogical-genetic classification schemes for volatile-rich ultramafic rocks. Groundmass spinel compositions are transitional between magnesian ulvöspinel (a Group-1 kimberlite hallmark feature) and titanomagnetite trends, the latter being more diagnostic for lamproite, orangeite (formerly Group-2 kimberlite), and aillikite. The Premier kimberlite dykes contain groundmass phlogopite that evolves by Al- and Ba-depletion to tetraferriphlogopite, a compositional trend that is more typical for orangeite and aillikite. Although high-pressure cognate and groundmass ilmenites from the Premier hypabyssal kimberlites are characteristically Mg-rich (up to 15?wt% MgO), they contain up to 5?wt% MnO, which is more typical for carbonate-rich magmatic systems such as aillikite and carbonatite. Manganese-rich groundmass ilmenite also occurs in the Premier carbonatite dykes, which are largely devoid of mantle-derived crystal cargo, suggesting a link to the kimberlite dykes by fractionation processes involving development of residual carbonate-rich melts and fluids. Although mineralogical-genetic classification schemes for kimberlites and related rocks may provide an elegant approach to circumvent common issues such as mantle debris entrainment, many of the key mineral compositional trends are not as robust for magma type identification as previously thought. Utilizing an experimentally constrained CO2-degassing model, it is suggested that the Premier kimberlite dykes have lost between 10 and 20?wt% CO2 during magma ascent through the cratonic lithosphere, prior to emplacement near the Earth's surface. Comparatively low fO2 values down to ?5.6 ?NNO are obtained for the kimberlite dykes when applying monticellite and perovskite oxybarometry, which probably reflects significant CO2 degassing during magma ascent rather than the original magma redox conditions and those of the deep upper mantle source. Thus, groundmass mineral oxybarometry may have little value for the prediction of the diamond preservation potential of ascending kimberlite magmas. After correction for olivine fractionation and CO2-loss, there remains a wide gap between the primitive kimberlite and carbonatite melt compositions at Premier, which suggests that these magma types cannot be linked by variably low degrees of partial melting of the same carbonated peridotite source in the deep upper mantle. Instead, fractionation processes produced carbonate-rich residual melts/fluids from ascending kimberlite magma, which led to the carbonatite dykes within Premier pipe.
Geostandards and Geoanalytical Research, in press available, 16p.
Australia
deposit - Mud Tank
Abstract: Zircon megacrysts from the Mud Tank carbonatite, Australia, are being used in many laboratories as a reference material for LA?ICP?MS U?Pb dating and trace element measurement, and LA?MC?ICP?MS determination of Hf isotopes. We summarise a database of > 10000 analyses of Mud Tank zircon (MTZ), collected from 2000 to 2018 during its use as a secondary reference material for simultaneous U?Pb and trace element analysis, and for Hf?isotope analysis. Trace element mass fractions are highest in dark red?brown stones and lowest in colourless and gem?quality ones. Individual unzoned grains can be chemically homogeneous, while significant variations in trace element mass fraction are associated with oscillatory zoning. Chondrite?normalised trace element patterns are essentially parallel over large mass fraction ranges. A Concordia age of 731.0 ± 0.2 Ma (2s, n = 2272) is taken as the age of crystallisation. Some grains show lower concordant to mildly discordant ages, probably reflecting minor Pb loss associated with cooling and the Alice Springs Orogeny (450-300 Ma). Our weighted mean 176Hf/177Hf is 0.282523 ± 10 (2s, n = 9350); the uncertainties on this ratio reflect some heterogeneity, mainly between grains. A few analyses suggest that colourless grains have generally lower 176Hf/177Hf. MTZ is a useful secondary reference material for U?Pb and Hf?isotope analysis, but individual grains need to be carefully selected using CL imaging and tested for homogeneity, and ideally should be standardised by solution analysis.
Abstract:
Earth’s only active natrocarbonatite volcanism, occurring at Oldoinyo Lengai (OL), Tanzania, suggests that natrocarbonatite melts are formed through a unique geological process. In the East African Rift, the extinct Kerimasi (KER) volcano is a neighbor of OL and also contains nephelinites hosting melt and fluid inclusions that preserve the igneous processes associated with formation of natrocarbonatite melts. Here, we present evidence for the presence of coexisting nephelinite melt, fluorine-rich carbonate melt, and alkali carbonate fluid. The compositions of these phases differ from the composition of OL natrocarbonatites; therefore, it is unlikely that natrocarbonatites formed directly from one of these phases. Instead, mixing of the outgassing alkali carbonate fluid and the fluorine-rich carbonate melt can yield natrocarbonatite compositions at temperatures close to subsolidus temperatures of nephelinite (<630-650 °C). Moreover, the high halogen content (6-16 wt%) in the carbonate melt precludes saturation of calcite (i.e., formation of calciocarbonatite) and maintains the carbonate melt in the liquid state with 28-41 wt% CaO at temperatures ?600 °C. Our study suggests that alkali carbonate fluids and melts could have commonly formed in the geological past, but it is unlikely they precipitated calcite that facilitates fossilization. Instead, alkali carbonates likely precipitated that were not preserved in the fossil nephelinite rocks. Thus, alkali carbonate fluids and melts have been so far overlooked in the geological record because of the lack of previous detailed inclusion studies.
Abstract: We studied the petrography, mineralogy, thermobarometry and whole rock chemistry of 120 peridotite and pyroxenite xenoliths collected from the 156 - 138 Ma Chidliak kimberlites CH-1, -6, -7 and -44. The xenoliths have higher CaO contents relative to Al2O3, and high Al for a given Mg/Si ratio compared to other cratonic peridotites. We assign the complex Ca-Al systematics of the Chidliak peridotites to repeated episodes of Ca-rich, Si-poor metasomatism, which introduced clinopyroxene and garnet, and later replaced orthopyroxene and clinopyroxene with secondary clinopyroxene and monticellite. This carbonatitic metasomatism, manifest in formation of wehrlites, acted upon the entire sampled mantle depth on a regional scale, including the proximal blocks of the North Atlantic Craton and the Chidliak mantle, where clinopyroxene and garnet modes are uniformly and heterogeneously high in the ~ 110 km deep mantle segment. Another, more recent type of mantle metasomatism, is expressed as elevated Ti in clinopyroxene and elevated Na and Ti in garnet, typical of sheared peridotites from CH-1, -7, and -44, but absent from CH-6 xenolith suite. The Ti-Na imprint is most intense in xenoliths derived from depths equivalent to 5.5 to 6.5 GPa, where it is associated with higher strain, the presence of sheared peridotites and higher temperatures varying isobarically by up to 200 °C. The horizontal scale of the thermal-metasomatic imprint is more ambiguous and could be as regional as 10's of kilometers or as local as < 1 km. The latter is constrained by the varied abundance of Ti-enriched garnets within a single kimberlite. The time-scale of this metasomatism relates to a conductive length-scale and could be as short as 100's ka, shortly predating the kimberlite formation. The Ti-Na, megacryst-like metasomatism may have resulted from a highly localized influx of hot hydrous proto-kimberlite fluids that weakened the mantle and triggered the formation of sheared peridotites.
Abstract: In October 2018, a diamond weighing a remarkable 552.7 ct was recovered from the Diavik mine in Canada. This is by far the largest known gem diamond found to date in North America. It is nearly three times larger than the 187.63 ct Diavik Foxfire which was unearthed from the same mine in August 2015, and about twice the size of a 271 ct white diamond mined from the Victor mine in Canada. GIA’s New York laboratory had the opportunity to examine this notable diamond in late January 2019, before it went on public display at the Phillips Auctions in New York...(no abstract, full article)
Abstract: The enigmatic appearance of cuboctahedral diamonds in ophiolitic and arc volcanic rocks with morphology and infrared characteristics similar to synthetic diamonds that were grown from metal solvent requires a critical reappraisal. We have studied 15 diamond crystals and fragments from Tolbachik volcano lava flows, using Fourier transform infrared spectrometry (FTIR), transmission electron microscopy (TEM), synchrotron X-ray fluorescence (SRXRF) and laser ablation inductively coupled plasma mass-spectrometry (LA-ICP-MS). FTIR spectra of Tolbachik diamonds correspond to typical type Ib patterns of synthetic diamonds. In TEM films prepared using focused ion beam technique, we find Mn-Ni and Mn-Si inclusions in Tolbachik diamonds. SRXRF spectra indicate the presence of Fe-Ni and Fe-Ni-Mn inclusions with Cr, Ti, Cu, and Zn impurities. LA-ICP-MS data show variable but significantly elevated concentrations of Mn, Fe, Ni, and Cu reaching up to 70?ppm. These transition metal concentration levels are comparable with those determined by LA-ICP-MS for similar diamonds from Tibetan ophiolites. Mn-Ni (+Fe) solvent was widely used to produce industrial synthetic diamonds in the former USSR and Russia with very similar proportions of these metals. Hence, it appears highly probable that the cuboctahedral diamonds recovered from Kamchatka arc volcanic rocks represent contamination and are likely derived from drilling tools or other hard instruments. Kinetic data on diamond dissolution in basaltic magma or in fluid phase demonstrate that diamond does not form under the pressures and temperature conditions prevalent within the magmatic system beneath the modern-day Klyuchevskoy group of arc volcanoes. We also considered reference data for inclusions in ophiolitic diamonds and compared them with the composition of solvent used in industrial diamond synthesis in China. The similar inclusion chemistry close to Ni70Mn25Co5 for ophiolitic and synthetic Chinese diamonds scrutinized here suggests that most diamonds recovered from Tibetan and other ophiolites are not natural but instead have a synthetic origin. In order to mitigate further dubious reports of diamonds from unconventional tectonic settings and source rocks, we propose a set of discrimination criteria to better distinguish natural cuboctahedral diamonds from those produced synthetically in industrial environments and found as contaminants in mantle- and crust-derived rocks.
Abstract: We propose to study the Kipawa peralkaline complex, a rare-earth deposit principally composed of eudialyte, mosandrite and britholite. The Kipawa complex is situated in the Parautochton zone of the Grenville Province in the Tesmiscamingue region of Quebec, 55 km south of contact with Superior Province. The complex consists of peralkaline syenites, amphibolites, gneisses that are intercalated with calc-silicate rocks and marble, and overlain by a peralkaline gneissic granite. The Kipawa complex differs geochemically and petrologically from other well-known peralkaline complexes such as the Illimausaq, Lovozero, Thor Lake or Strange Lake complexes. Classic peralkaline complexes are large, circular igneous complexes, with or without volcanism and have an isotopic signature reflecting mantle origin with different degrees of assimilation and crustal contamination (for example Illimausaq is reported with ?Nd values of 0.4 and -5.7). The Kipawa Complex is a thin, folded stack of sheet imbricates between Kikwissi Suite rocks, McKillop Lake sequence and Red Pine Chute gneiss, suggesting a regional tectonic control. Isotopic analyses carried out by other teamsindicate a strong crustal signature (?Nd = -8.7). Several hypotheses are possible: crustal contamination, hydrothermal activity, fluids alteration during formation, metamorphism or dominant crustal origin. Our objective is to characterize the geochemical and isotopic composition of the Kipawa complex in order to improve our understanding of the age and formation of the complex. Analyses of both whole rocks, eudialytes and zircons will be made to obtain isotopic signatures and determine formation ages and/or post-formation processes.
Abstract: We sampled the mid-Ediacaran Saint-Honoré alkali intrusion and related dykes in the Saguenay City region of Québec for paleomagnetic and U-Pb, 40Ar/39Ar geochonologic study. 40Ar/39Ar geochronology of phlogopite separates from carbonatite of the central intrusion return plateau ages with a weighted mean of 578.3 ± 3.5 Ma. Baddeleyite from a phoscorite dyke provides a concordant age of 580.25 ± 0.87 Ma for the crystallization of the dykes associated with the St-Honoré intrusive complex. Paleomagnetic results from the intrusion itself and related carbonatite and lamprophyre dykes exhibit some streaking between higher to moderate inclination directions, even at the site level, after screening to remove a steep, present-day viscous remanence. The predominant St-Honoré mean direction (13 sites), which is primary (baked contact test on the host Lac St-Jean anorthosite), is D = 119, I = 72.3°; ?95 = 9.5°, retained at higher coercivity and to high unblocking temperatures by titanomagnetite. Assuming a geocentric axial dipole, this result places the St. Honoré locality at 57° S at ~ 580 Ma, implying that Laurentia straddled mid-paleolatitudes at that time. Notably, the paleopole location at 27.2° N, 320.7 E (dp = 15°, dm = 17°) is consistent with similar mid-Ediacaran age paleopoles which place Laurentia at mid- to high paleolatitudes. The Saint-Honoré result implies that Laurentia had moved from low latitude in the early Ediacaran to higher southern paleolatitudes by 580-570 Ma, and then back to low paleolatitudes by as early as 564 Ma. Viewed as apparent polar wander (APW), this motion traces an 'Ediacaran loop' that can also be seen in similar-aged paleomagnetic results from at least two other paleocontinents. The similar APW loops suggest a role for true polar wander in Ediacaran geodynamics, and perhaps help to define a longitudinally-constrained global Ediacaran paleogeography.
Abstract: The Good Hope carbonatite is located adjacent to the Prairie Lake ijolite-malignite-calcite carbonatite complex in northwestern Ontario. The carbonatite is a breccia consisting of diverse calcite and dolomite carbonatites, with lesser REE-rich ferrocarbonatites, containing xenoliths of amphibole syenite, potassium feldspar+phlogopite and pyrochlore-apatite cumulates. The occurrence outcrops over an area of 500 m x 500 m and has been proven by diamond drilling to extend to a minimum depth of 650 m. Pyrochlore-apatite cumulates occur as elongated and/or irregular clasts up to 5 cm in maximum dimension. In these, pyrochlore has crystallized before apatite and occurs as euhedral crystals (0.1-1 cm; up to 5 cm) and can comprise up to ca. 25 vol % of a clast. Prismatic apatite is commonly flow-aligned and in some instances forms isoclinal folds. The apatite does not exhibit optical- or BSE-compositional zonation. However, cathodoluminescence imagery shows blue-green cores with thin (< 500 ?m) blue margins. The cores are enriched in light REE (833-941 ppm La; 1790-2200 ppm Ce; 8.2-13.6 Yb ppm; (La/Yb)CN 62-42. The pyrochlores are Na-Ca-F-pyrochlore of relatively-uniform composition with fully-occupied A-sites, and minor SrO (l-1.5 wt %) and low Ta2O5 (< 0.5 wt %). Some pyrochlores have irregular cores of resorbed Sr-bearing (6-11 wt % SrO) pyrochlore with overgrowths of Na-Ca-F-pyrochlore. Others contain inclusions of fersmite and/or columbite-(Fe). Pyrochlore also occurs as discrete crystals in calcite and dolomite hosts and represents disaggregated clasts. In accord with experimental data on the liquidus phase relationships of apatite and pyrochlore in haplocarbonatite melts the formation of apatite-pyrochlore cumulates in the initial stages of crystallization of such melts is to be expected. These cumulates were subsequently disrupted, disaggregated, and transported by pulses of later batches of carbonatite of diverse composition.
Abstract: Kimberlites often entrain crustal felsic xenoliths, which show alteration and metamorphism as a result of interaction with the host kimberlite. We studied granite and gneiss xenoliths in the Renard 65 kimberlite pipe (Northern Québec, Canada). The study comprised a detailed petrographic examination of 45 thin sections, a scanning electron microscopy and an X-ray powder diffractometry of a sample sub-set. Two major units of the Renard 65 pipe (Unit A and Unit B/D) distinguished by abundance of crustal xenoliths along with the degree of their alteration, were investigated. Unit A is a volcaniclastic kimberlite with 40-90 % xenoliths, whereas Unit B/D is a hypabyssal kimberlite with textures transitional to pyroclastic, containing 15-40 % more intensely altered xenoliths. Both units carry xenoliths of coarse-grained leucogranite (K-feldspar, plagioclase, quartz, biotite with accessory garnet, apatite, and zircon) and medium-grained gneiss (plagioclase, quartz, biotite, orthopyroxene with accessory garnet, apatite and zircon). The Unit A xenoliths are partially replaced by chlorite, sericite, epidote, serpentine, richterite, actinolite and clinochlore vermiculite. In Unit B/D four distinct metamorphic and metasomatic mineral assemblages almost completely replace xenoliths. The assemblages include aegirine, pectolite, garnet, wollastonite, xonotlite, prehnite, calcite, K-feldspar and richterite in various proportions. Secondary K-feldspar and calcite may indicate the granite protolith, whereas wollastonite may be the signature of the gneiss protolith. The presence of secondary garnet and wollastonite, the hallmark skarn minerals, suggests the analogy between the classical skarn geological processes at the contact between felsic rocks and the host hot carbonate-rich melts. The observed mineralogy of the Renard 65 felsic xenoliths will be compared with the theoretically predicted mineralogy modelled using Theriak-Domino or Perplex software for the known bulk hybrid kimberlite compositions. The comparison will enable constraints on temperatures, volatile contents and thermal history of the kimberlite melt during emplacement.
Abstract: Geometallurgy aims to develop and deploy predictive spatial models based on tangible and quantitative resource characteristics that are used to optimize the efficiency of minerals beneficiation and extractive metallurgy operations. Whilst most current applications of geometallurgy are focused on the major commodity to be recovered from a mineral deposit, this contribution delineates the opportunity to use a geometallurgical approach to provide an early assessment of the economic potential of by-product recovery from an ongoing mining operation. As a case study for this methodology possible REE-recovery as a by-product of Nb-production at the Catalão I carbonatite complex, the Chapadão mine is used. Catalão I is part of the Alto Paranaíba Igneous Province in the Goias Province of Brazil. Nowadays, niobium is produced in the complex as a by-product of the Chapadão phosphates mine. This production is performed on the Tailings plant, the focus of this study. Rare earth elements, albeit present in significant concentrations, are currently not recovered as by-products. Nine samples from different stages of the Nb beneficiation process in the Tailings plant were taken and characterized by Mineral Liberation Analyzer, X-ray powder diffraction, and bulk rock chemistry. The recovery of rare earth elements in each of the tailing streams was quantified by mass balance. The quantitative mineralogical and microstructural data are used to identify the most suitable approach to recover REE as a by-product-without placing limitations on niobium production. Monazite, the most common rare earth mineral identified in the feed, occurs as Ce-rich and La-rich varieties that can be easily distinguished by SEM-based image analysis. Quartz, FeTi-oxides and several phosphate minerals are the main gangue minerals. The highest rare earth oxide content concentrations (1.75 wt.% TREO) and the greatest potential for REE processing are reported for the final flotation tailings stream. To place tentative economic constraints on REE recovery from the tailings material, an analogy to the Browns Range deposit in Australia is drawn. Its technical flow sheet was used to estimate the cost for a hypothetical REE-production at Chapadão. Parameters derived from SEM-based image analysis were used to model possible monazite recovery and concentrate grades. This exercise illustrates that a marketable REE concentrate could be obtained at Chapadão if the process recovers at least 53 % of the particles with no less than 60% of monazite on their surface. Applying CAPEX and OPEX values similar to that of Browns Range suggest that such an operation would be profitable at current REE prices.
Abstract: Subsolidus and melting phase relationships in the system Na2CO3-CaCO3-MgCO3 have been studied at 6?GPa and 900-1250?°C using a Kawai-type multianvil press. At 900 and 1000?°C, the system has four intermediate compounds: Na2Ca4(CO3)5 burbankite, Na2Ca3(CO3)4, Na4Ca(CO3)3, and Na2Mg(CO3)2 eitelite. The Na-Ca compounds dissolve noticeable amounts of Mg component, whereas eitelite dissolves a few percents of Ca component: Na2(Ca?0.91Mg?0.09)4(CO3)5, Na2(Ca?0.94Mg?0.06)3(CO3)4, Na4(Ca?0.67Mg?0.33)(CO3)3, and Na2(Mg?.93Ca?0.07)(CO3)2. At 1050?°C, the system is complicated by an appearance of dolomite. Na-Ca burbankite decomposes at 1075?±?25?°C to aragonite plus Na2Ca3(CO3)4. Na4Ca(CO3)3 and eitelite disappear via congruent melting between 1200 and 1250?°C. Na2Ca3(CO3)4 remains stable through the whole studied temperature range. The liquidus projection of the studied ternary system has eight primary solidification phase regions for magnesite, dolomite, calcite-dolomite solid solutions, aragonite, Na2Ca3(CO3)4, Na4Ca(CO3)3, and Na2CO3 solid solutions. The system has five ternary peritectic reaction points and one minimum on the liquidus at 1050?°C and 48Na2CO3•52(Ca0.75Mg0.25)CO3. The minimum point resembles a eutectic controlled by a four-phase reaction, by which a liquid transforms into three solid phases upon cooling: Na2(Ca0.94Mg0.06)3(CO3)4, Na4(Ca0.67Mg0.33)(CO3)3, and Na2(Mg0.93Ca0.07)(CO3)2 eitelite. Since at 6?GPa, the system has a single eutectic, there is no thermal barrier preventing continuous liquid fractionation from alkali-poor toward Na-rich dolomitic compositions. Cooling of the Na-Ca-Mg carbonatite melt from 1400 to 1100?°C within the lherzolite substrate will be accompanied by magnesite crystallization and wehrlitization keeping calcium number of the melt at 40 and shifting the Na2CO3 content to ?40?mol%. In the case of the eclogitic wall rock, the cooling will be accompanied by dolomite crystallization keeping calcium number of the melt at 60-65 and shifting the Na2CO3 content to ?30?mol%.
Abstract: Large-ion lithophile elements (LILE)-enriched chromium titanates of the magnetoplumbite (AM12O19) and crichtonite (ABC18T2O38) groups have been recognized as abundant inclusions in orthopyroxene grains in a mantle-derived xenolith from the Udachnaya-East kimberlite pipe, Daldyn field, Siberian craton. The studied xenolith consists of three parts: an orthopyroxenite, a garnet clinopyroxenite, and a garnet-orthopyroxene intermediate domain between the two. Within the host enstatite (Mg# 92.6) in the orthopyroxenitic part of the sample titanate inclusions are associated with Cr-spinel, diopside, rutile, Mg-Cr-ilmenite, and pentlandite. Crichtonite-group minerals also occur as acicular inclusions in pyrope grains of the intermediate domain adjacent to the orthopyroxenite, as well as in interstitial to enstatite oxide intergrowths together with Cr-spinel, rutile, and ilmenite. Yimengite-hawthorneite inclusions in enstatite contain (wt%) 3.72-8.04 BaO, 2.05-3.43 K2O, and 0.06-0.48 CaO. Their composition is transitional between yimengite and hawthorneite end-members with most grains exhibiting K-dominant chemistry. A distinct feature of the studied yimengitehawthorneite minerals is a high content of Al2O3 (5.74-7.69 wt%). Crichtonite-group minerals vary in compositions depending on the occurrence in the xenolith: inclusions in enstatite are moderate-high in TiO2 (62.9-67.1 wt%), moderately Cr-rich (12.6-14.0 wt% Cr2O3), Ba- or K-specific in the A site, and contain low ZrO2 (0.05-1.72 wt%), whereas inclusions in pyrope are moderate in TiO2 (61.7-63.3 wt% TiO2), relatively low in Cr (8.98-9.62 wt% Cr2O3), K-dominant in the A site, and are Zr-enriched (4.64-4.71 wt% ZrO2). Crichtonite-group minerals in polymineralic oxide intergrowths show highly diverse compositions even within individual aggregates, where they are chemically dominated by Ba, Ca, and Sr. P-T estimates indicate the orthopyroxenite to have equilibrated at ~800 °C and 35 kbar. Preferentially oriented lamellae of enstatite-hosted Cr-spinel and diopside, as well as pyrope, diopside, and Cr-spinel grains developed around enstatite crystals, are interpreted to have been exsolved from the high-T Ca-Al-Cr-enriched orthopyroxene precursor. The exotic titanate compositions and observed textural relationships between inclusions in enstatite imply that the studied orthopyroxenite has undergone metasomatic processing by a mobile percolating agent afterward; this highly evolved melt/fluid was enriched in Ba, K, HFSE, and other incompatible elements. The infiltration of the metasomatizing liquid occurred through interstices and vulnerable zones of enstatite grains and manifested in the crystallization of titanate inclusions. It is assumed that Cr-spinel lamellae served as seeds for their nucleation and growth. The prominent textural and chemical inhomogeneity of the interstitial oxide intergrowths is either a consequence of the metasomatic oxide crystallization shortly prior to the kimberlite magma eruption or arose from the intensive modification of preexisting oxide clusters by the kimberlite melt during the Udachnaya emplacement. Our new data provide implications for the metasomatic treatment of orthopyroxenites in the subcontinental lithospheric mantle from the view of exotic titanate occurrences.
Abstract: The tectonic setting of northeastern Angola was influenced by the opening of the South Atlantic Ocean, which reactivated deep NE-SW-trending faults during the early Cretaceous. The new interpretation of a kimberlitic pulse during the middle of the Aptian and the Albian, which provides precise data on the age of a significant diamond-bearing kimberlite pulse in Angola, will be an important guide in future diamond exploration. These findings contribute to a better understanding of the petrogenetic evolution of the kimberlites in northeastern Angola and have important implications for diamond exploration. Six kimberlite pipes within the Lucapa structure in northeastern Angola have been investigated using major and trace element geochemistry of mantle xenoliths, macro- and megacrysts. Geothermobarometric calculations were carried out using xenoliths and well-calibrated single crystals of clinopyroxene. Geochronological and isotopic studies were also performed where there were samples available of sufficient quality. Results indicate that the underlying mantle experienced variable conditions of equilibration among the six sites. Subsequent metasomatic enrichment events also support a hypothesis of different sources for these kimberlites. The U/Th values suggest at least two different sources of zircon crystals from the Catoca suite. These different populations may reflect different sources of kimberlitic magma, with some of the grains produced in U- and Th-enriched metasomatized mantle units, an idea consistent with the two populations of zircon identified on the basis of their trace element compositions. This research shows the absence of fresh Mg-rich ilmenite in the Catoca kimberlite (one of the largest bodies of kimberlite in the world), as well as the occurrence of Fe3+-rich ilmenite, do not exclude the presence of diamond in the kimberlite. This is a new insight into the concept of ilmenite and diamond exploration and leads to the conclusion that compositional attributes must be evaluated in light of textural attributes.
Abstract: This study investigates the major and trace element composition of minerals of the ijolite series rocks occurring at the Prairie Lake Carbonatite Complex, northern Ontario, together with comparative data with ijolites from the Fen complex, Norway. Trace element data (Sr, Zr, REE) were collected by LA-ICP-MS for clinopyroxene, garnet, and apatite, and in conjunction with the major element data are used to develop a petrogenetic model for Prairie Lake. The ijolites and calcite ijolites (hollaites) of Prairie Lake Carbonatite Complex have been formed by magma mixing, crystal settling, solid-state deformation, and deuteric alteration. The complex represents at least three stages of intrusion by melts of differing composition. The initial stage is predominantly biotite pyroxenite and associated coarse carbonatite veins. The second stage is primarily members of the ijolite series together with solid state deformation creating meta-ijolites, with differentiation forming malignites (potassic nepheline syenites). The third major stage is the intrusion of the CII carbonatites derived from different batches of magmas. These rocks contain xenoliths of ijolite suite rocks and phoscorites. Pyroxene compositions show an evolutionary trend from diopside in biotite pyroxenites to Fe enriched diopside-augite in ijolites, to aegirine in malignites. These data are used to show that a continuously filled fractionating magma chamber was not present at Prairie lake and that the complex formed as result of small intrusions of nephelinite into pre-existing ijolites. A similar style of petrogenesis is suggested for the Fen complex.
Abstract: Zircon from Tomtor syenites and kamaphorites was dated following the U-Pb method (SHRIMP-II), and the distribution of trace and rare-earth elements (REE) was studied at the same zircon point using an ion microprobe. The main zircon population from syenites was dated at 402?±?7 Ma, while the age range of single zircon grains was 700-660 M?. Different-aged zircon groups from syenites exhibited the characteristics of magmatic zircon, but their concentrations of REE and other trace elements differed markedly. The REE distribution in 700-660-M? zircon is consistent with that of the typical zircon from syenites (Belousova et al., 2002), while the heavy rare-earth elements (HREE), P, Ti, and Y concentrations of ca. 400-Ma zircon differ from those of older zircon. This is the first isotope-geochemical study of zircon from kamaphorites, and the U-Pb age of ca. 400 M? is within the error limits with of the main zircon population from syenites. The considerable enrichment of REE, C?, Ti, Sr, Y, Nb, and Ba in zircon from kamaphorites may be partly due to the presence of burbankite microinclusions. The trace-element distribution pattern of zircon from kamaphorites is very similar to the geochemical characteristics of zircon from Tiksheozero carbonatites (Tichomirowa et al., 2013). The new age dates for Tomtor syenites and kamaphorites, consistent with 700-660 M? and ca. 400 M? events, support the zircon (Vladykin et al., 2014) and pyrochlore (Antonov et al., 2017) age dates determined following the U-Pb method and those of biotite obtained following the 40Ar-39Ar method (Vladykin et al., 2014).
Abstract: Five typical coated diamonds (from Udachnaya, Yubileynaya, and Aikhal kimberlite pipes) with untypically low microinclusion abundances and four monocrystalline diamonds (Udachnaya, Mir, Nyurbinskaya pipes) that exhibit thin intermediate microinclusion-bearing zones were examined in details for growth structures, characteristic infrared absorption and photoluminescence, and composition of microinclusions. The internal structures of diamonds of both types imply that fluid inclusions entrapment in diamonds does not necessarily relate to the terminal stage of rapid fibrous growth. Instead, nitrogen aggregation state in some diamonds showed that both fibrous coats and inclusion-bearing layers might experience an annealing during mantle residence long enough to pre-date the ultimate kimberlite eruption, whereas the diamonds with internal inclusion-bearing zones also experienced later protracted history of monocrystalline growth. The presence of chloride-carbonate-silicate fluids/melts in monocrystalline diamonds indicate their generation from media generally similar to that observed in some fibrous diamonds. However, the composition of these metasomatizing fluids is different for the mantle beneath Udachnaya (mostly carbonatitic) and other pipes (Aikhal, Yubileynaya, Mir; variable abundance of silicic high-density fluids). The abundance of silica-rich fluids record either a heterogeneous distribution of eclogites in the subcontinental lithospheric mantle, or the operation of silica-rich slab-derived fluids. The inclusion abundance as well as the type of growth (fibrous or monocrystalline) is considered to be controlled by the volume of fluid fluxes; in this case, fluid consumption leads to decreasing growth rates, diminishing inclusion entrainment and stability of layered octahedrons. The detected minor compositional variations of high-density fluids in these diamonds may be due to local scale thermal perturbation in the host source and/or limited chemical heterogeneity of the parental fluid. The high amount of chlorides in high-density fluids from monocrystalline diamonds provide a new evidence for compositions of fluids/melts acting as primary metasomatic agent in the deep mantle of Siberian craton.
Abstract: Five typical coated diamonds (from Udachnaya, Yubileynaya, and Aikhal kimberlite pipes) with untypically low microinclusion abundances and four monocrystalline diamonds (Udachnaya, Mir, Nyurbinskaya pipes) that exhibit thin intermediate microinclusion-bearing zones were examined in details for growth structures, characteristic infrared absorption and photoluminescence, and composition of microinclusions. The internal structures of diamonds of both types imply that fluid inclusions entrapment in diamonds does not necessarily relate to the terminal stage of rapid fibrous growth. Instead, nitrogen aggregation state in some diamonds showed that both fibrous coats and inclusion-bearing layers might experience an annealing during mantle residence long enough to pre-date the ultimate kimberlite eruption, whereas the diamonds with internal inclusion-bearing zones also experienced later protracted history of monocrystalline growth. The presence of chloride-carbonate-silicate fluids/melts in monocrystalline diamonds indicate their generation from media generally similar to that observed in some fibrous diamonds. However, the composition of these metasomatizing fluids is different for the mantle beneath Udachnaya (mostly carbonatitic) and other pipes (Aikhal, Yubileynaya, Mir; variable abundance of silicic high-density fluids). The abundance of silica-rich fluids record either a heterogeneous distribution of eclogites in the subcontinental lithospheric mantle, or the operation of silica-rich slab-derived fluids. The inclusion abundance as well as the type of growth (fibrous or monocrystalline) is considered to be controlled by the volume of fluid fluxes; in this case, fluid consumption leads to decreasing growth rates, diminishing inclusion entrainment and stability of layered octahedrons. The detected minor compositional variations of high-density fluids in these diamonds may be due to local scale thermal perturbation in the host source and/or limited chemical heterogeneity of the parental fluid. The high amount of chlorides in high-density fluids from monocrystalline diamonds provide a new evidence for compositions of fluids/melts acting as primary metasomatic agent in the deep mantle of Siberian craton.
Abstract: Five typical coated diamonds (from Udachnaya, Yubileynaya, and Aikhal kimberlite pipes) with untypically low microinclusion abundances and four monocrystalline diamonds (Udachnaya, Mir, Nyurbinskaya pipes) that exhibit thin intermediate microinclusion-bearing zones were examined in details for growth structures, characteristic infrared absorption and photoluminescence, and composition of microinclusions. The internal structures of diamonds of both types imply that fluid inclusions entrapment in diamonds does not necessarily relate to the terminal stage of rapid fibrous growth. Instead, nitrogen aggregation state in some diamonds showed that both fibrous coats and inclusion-bearing layers might experience an annealing during mantle residence long enough to pre-date the ultimate kimberlite eruption, whereas the diamonds with internal inclusion-bearing zones also experienced later protracted history of monocrystalline growth. The presence of chloride-carbonate-silicate fluids/melts in monocrystalline diamonds indicate their generation from media generally similar to that observed in some fibrous diamonds. However, the composition of these metasomatizing fluids is different for the mantle beneath Udachnaya (mostly carbonatitic) and other pipes (Aikhal, Yubileynaya, Mir; variable abundance of silicic high-density fluids). The abundance of silica-rich fluids record either a heterogeneous distribution of eclogites in the subcontinental lithospheric mantle, or the operation of silica-rich slab-derived fluids. The inclusion abundance as well as the type of growth (fibrous or monocrystalline) is considered to be controlled by the volume of fluid fluxes; in this case, fluid consumption leads to decreasing growth rates, diminishing inclusion entrainment and stability of layered octahedrons. The detected minor compositional variations of high-density fluids in these diamonds may be due to local scale thermal perturbation in the host source and/or limited chemical heterogeneity of the parental fluid. The high amount of chlorides in high-density fluids from monocrystalline diamonds provide a new evidence for compositions of fluids/melts acting as primary metasomatic agent in the deep mantle of Siberian craton.
Abstract: Five typical coated diamonds (from Udachnaya, Yubileynaya, and Aikhal kimberlite pipes) with untypically low microinclusion abundances and four monocrystalline diamonds (Udachnaya, Mir, Nyurbinskaya pipes) that exhibit thin intermediate microinclusion-bearing zones were examined in details for growth structures, characteristic infrared absorption and photoluminescence, and composition of microinclusions. The internal structures of diamonds of both types imply that fluid inclusions entrapment in diamonds does not necessarily relate to the terminal stage of rapid fibrous growth. Instead, nitrogen aggregation state in some diamonds showed that both fibrous coats and inclusion-bearing layers might experience an annealing during mantle residence long enough to pre-date the ultimate kimberlite eruption, whereas the diamonds with internal inclusion-bearing zones also experienced later protracted history of monocrystalline growth. The presence of chloride-carbonate-silicate fluids/melts in monocrystalline diamonds indicate their generation from media generally similar to that observed in some fibrous diamonds. However, the composition of these metasomatizing fluids is different for the mantle beneath Udachnaya (mostly carbonatitic) and other pipes (Aikhal, Yubileynaya, Mir; variable abundance of silicic high-density fluids). The abundance of silica-rich fluids record either a heterogeneous distribution of eclogites in the subcontinental lithospheric mantle, or the operation of silica-rich slab-derived fluids. The inclusion abundance as well as the type of growth (fibrous or monocrystalline) is considered to be controlled by the volume of fluid fluxes; in this case, fluid consumption leads to decreasing growth rates, diminishing inclusion entrainment and stability of layered octahedrons. The detected minor compositional variations of high-density fluids in these diamonds may be due to local scale thermal perturbation in the host source and/or limited chemical heterogeneity of the parental fluid. The high amount of chlorides in high-density fluids from monocrystalline diamonds provide a new evidence for compositions of fluids/melts acting as primary metasomatic agent in the deep mantle of Siberian craton.
Abstract: Five typical coated diamonds (from Udachnaya, Yubileynaya, and Aikhal kimberlite pipes) with untypically low microinclusion abundances and four monocrystalline diamonds (Udachnaya, Mir, Nyurbinskaya pipes) that exhibit thin intermediate microinclusion-bearing zones were examined in details for growth structures, characteristic infrared absorption and photoluminescence, and composition of microinclusions. The internal structures of diamonds of both types imply that fluid inclusions entrapment in diamonds does not necessarily relate to the terminal stage of rapid fibrous growth. Instead, nitrogen aggregation state in some diamonds showed that both fibrous coats and inclusion-bearing layers might experience an annealing during mantle residence long enough to pre-date the ultimate kimberlite eruption, whereas the diamonds with internal inclusion-bearing zones also experienced later protracted history of monocrystalline growth. The presence of chloride-carbonate-silicate fluids/melts in monocrystalline diamonds indicate their generation from media generally similar to that observed in some fibrous diamonds. However, the composition of these metasomatizing fluids is different for the mantle beneath Udachnaya (mostly carbonatitic) and other pipes (Aikhal, Yubileynaya, Mir; variable abundance of silicic high-density fluids). The abundance of silica-rich fluids record either a heterogeneous distribution of eclogites in the subcontinental lithospheric mantle, or the operation of silica-rich slab-derived fluids. The inclusion abundance as well as the type of growth (fibrous or monocrystalline) is considered to be controlled by the volume of fluid fluxes; in this case, fluid consumption leads to decreasing growth rates, diminishing inclusion entrainment and stability of layered octahedrons. The detected minor compositional variations of high-density fluids in these diamonds may be due to local scale thermal perturbation in the host source and/or limited chemical heterogeneity of the parental fluid. The high amount of chlorides in high-density fluids from monocrystalline diamonds provide a new evidence for compositions of fluids/melts acting as primary metasomatic agent in the deep mantle of Siberian craton.
Geochimica et Cosmochimica Acta, in press available 29p.
Africa, South Africa, Botswana
deposit - Koffiefontein, Letlhakane, Orapa, Finsch, De Beers Pool
Abstract: Ten individual gem-quality monocrystalline diamonds of known peridotite/eclogite paragenesis from Southern Africa (Koffiefontein, Letlhakane, Orapa) were studied for trace element concentrations and He and Ar abundances and isotopic compositions. In addition, two samples, consisting of pooled fragments of gem-quality peridotitic diamonds from Finsch and DeBeers Pool respectively, were analysed for noble gases. Previous studies (Richardson et al., 1984; Pearson et al., 1998; Gress et al., 2017; Timmerman et al., 2017) provided age constraints of 0.09, 1.0-1.1, 1.7, 2.3, and 3.2-3.4?Ga on mineral inclusions in the studied diamonds, allowing us to study trace elements and noble gases over 3 Gyr of geological time. Concentrations of trace elements in the diamonds are very low - a few hundred ppt to several tens of ppbs - and are likely dependent on the amount of sub-micron inclusions present. Trace element patterns and trace element/3He ratios of the studied monocrystalline diamonds are similar to those in fibrous diamonds, suggesting that trace elements and stable noble gas isotopes reside within the same locations in diamond and track the same processes that are reflected in the trace element patterns. We cannot discern any temporal differences in these geochemical tracers, suggesting that the processes generating them have been occurring over at least the past 2.3?Ga. 3He/4He ratios decrease and 4He and 40Ar* contents increase with increasing age of peridotitic and some eclogitic diamonds, showing the importance of in-situ radiogenic 4He and 40Ar ingrowth by the decay of U-Th-Sm and K respectively. For most gem-quality monocrystalline diamonds, uncertainties in the 3He/4He evolution of the continental lithospheric mantle combined with large analytical uncertainties and possible spatial variability in U-Th-Sm concentrations limit our ability to provide estimates of diamond formation ages using 4He ingrowth. However, the limited observed 4He ingrowth (low U?+?Th/3He) together with a R/Ra value of 5.3 for peridotitic diamond K306 is comparable to the present-day sub-continental lithospheric mantle value and supports the young diamond formation age found by Re-Os dating of sulphides in the same diamond by Pearson et al. (1998). After correction for in-situ radiogenic 4He produced since diamond formation a large variation in 3He/4He remains in ?1?Ga old eclogitic diamonds that is suggested to result from the variable influence of subducted altered oceanic crust that has low 3He/4He. Hence, the 3He/4He isotope tracer supports an origin of the diamond-forming fluids from recycled oceanic crust for eclogitic diamonds, as indicated by other geochemical proxies.
Geochimica et Cosmochimica Acta, in press available 29p.
Africa, South Africa, Botswana
deposit - Koffiefontein, Letlhakane, Orapa, Finsch, De Beers Pool
Abstract: Ten individual gem-quality monocrystalline diamonds of known peridotite/eclogite paragenesis from Southern Africa (Koffiefontein, Letlhakane, Orapa) were studied for trace element concentrations and He and Ar abundances and isotopic compositions. In addition, two samples, consisting of pooled fragments of gem-quality peridotitic diamonds from Finsch and DeBeers Pool respectively, were analysed for noble gases. Previous studies (Richardson et al., 1984; Pearson et al., 1998; Gress et al., 2017; Timmerman et al., 2017) provided age constraints of 0.09, 1.0-1.1, 1.7, 2.3, and 3.2-3.4?Ga on mineral inclusions in the studied diamonds, allowing us to study trace elements and noble gases over 3 Gyr of geological time. Concentrations of trace elements in the diamonds are very low - a few hundred ppt to several tens of ppbs - and are likely dependent on the amount of sub-micron inclusions present. Trace element patterns and trace element/3He ratios of the studied monocrystalline diamonds are similar to those in fibrous diamonds, suggesting that trace elements and stable noble gas isotopes reside within the same locations in diamond and track the same processes that are reflected in the trace element patterns. We cannot discern any temporal differences in these geochemical tracers, suggesting that the processes generating them have been occurring over at least the past 2.3?Ga. 3He/4He ratios decrease and 4He and 40Ar* contents increase with increasing age of peridotitic and some eclogitic diamonds, showing the importance of in-situ radiogenic 4He and 40Ar ingrowth by the decay of U-Th-Sm and K respectively. For most gem-quality monocrystalline diamonds, uncertainties in the 3He/4He evolution of the continental lithospheric mantle combined with large analytical uncertainties and possible spatial variability in U-Th-Sm concentrations limit our ability to provide estimates of diamond formation ages using 4He ingrowth. However, the limited observed 4He ingrowth (low U?+?Th/3He) together with a R/Ra value of 5.3 for peridotitic diamond K306 is comparable to the present-day sub-continental lithospheric mantle value and supports the young diamond formation age found by Re-Os dating of sulphides in the same diamond by Pearson et al. (1998). After correction for in-situ radiogenic 4He produced since diamond formation a large variation in 3He/4He remains in ?1?Ga old eclogitic diamonds that is suggested to result from the variable influence of subducted altered oceanic crust that has low 3He/4He. Hence, the 3He/4He isotope tracer supports an origin of the diamond-forming fluids from recycled oceanic crust for eclogitic diamonds, as indicated by other geochemical proxies.
Geochimica et Cosmochimica Acta, in press available 29p.
Africa, South Africa, Botswana
deposit - Koffiefontein, Letlhakane, Orapa, Finsch, De Beers Pool
Abstract: Ten individual gem-quality monocrystalline diamonds of known peridotite/eclogite paragenesis from Southern Africa (Koffiefontein, Letlhakane, Orapa) were studied for trace element concentrations and He and Ar abundances and isotopic compositions. In addition, two samples, consisting of pooled fragments of gem-quality peridotitic diamonds from Finsch and DeBeers Pool respectively, were analysed for noble gases. Previous studies (Richardson et al., 1984; Pearson et al., 1998; Gress et al., 2017; Timmerman et al., 2017) provided age constraints of 0.09, 1.0-1.1, 1.7, 2.3, and 3.2-3.4?Ga on mineral inclusions in the studied diamonds, allowing us to study trace elements and noble gases over 3 Gyr of geological time. Concentrations of trace elements in the diamonds are very low - a few hundred ppt to several tens of ppbs - and are likely dependent on the amount of sub-micron inclusions present. Trace element patterns and trace element/3He ratios of the studied monocrystalline diamonds are similar to those in fibrous diamonds, suggesting that trace elements and stable noble gas isotopes reside within the same locations in diamond and track the same processes that are reflected in the trace element patterns. We cannot discern any temporal differences in these geochemical tracers, suggesting that the processes generating them have been occurring over at least the past 2.3?Ga. 3He/4He ratios decrease and 4He and 40Ar* contents increase with increasing age of peridotitic and some eclogitic diamonds, showing the importance of in-situ radiogenic 4He and 40Ar ingrowth by the decay of U-Th-Sm and K respectively. For most gem-quality monocrystalline diamonds, uncertainties in the 3He/4He evolution of the continental lithospheric mantle combined with large analytical uncertainties and possible spatial variability in U-Th-Sm concentrations limit our ability to provide estimates of diamond formation ages using 4He ingrowth. However, the limited observed 4He ingrowth (low U?+?Th/3He) together with a R/Ra value of 5.3 for peridotitic diamond K306 is comparable to the present-day sub-continental lithospheric mantle value and supports the young diamond formation age found by Re-Os dating of sulphides in the same diamond by Pearson et al. (1998). After correction for in-situ radiogenic 4He produced since diamond formation a large variation in 3He/4He remains in ?1?Ga old eclogitic diamonds that is suggested to result from the variable influence of subducted altered oceanic crust that has low 3He/4He. Hence, the 3He/4He isotope tracer supports an origin of the diamond-forming fluids from recycled oceanic crust for eclogitic diamonds, as indicated by other geochemical proxies.
Geochimica et Cosmochimica Acta, in press available 29p.
Africa, South Africa, Botswana
deposit - Koffiefontein, Letlhakane, Orapa, Finsch, De Beers Pool
Abstract: Ten individual gem-quality monocrystalline diamonds of known peridotite/eclogite paragenesis from Southern Africa (Koffiefontein, Letlhakane, Orapa) were studied for trace element concentrations and He and Ar abundances and isotopic compositions. In addition, two samples, consisting of pooled fragments of gem-quality peridotitic diamonds from Finsch and DeBeers Pool respectively, were analysed for noble gases. Previous studies (Richardson et al., 1984; Pearson et al., 1998; Gress et al., 2017; Timmerman et al., 2017) provided age constraints of 0.09, 1.0-1.1, 1.7, 2.3, and 3.2-3.4?Ga on mineral inclusions in the studied diamonds, allowing us to study trace elements and noble gases over 3 Gyr of geological time. Concentrations of trace elements in the diamonds are very low - a few hundred ppt to several tens of ppbs - and are likely dependent on the amount of sub-micron inclusions present. Trace element patterns and trace element/3He ratios of the studied monocrystalline diamonds are similar to those in fibrous diamonds, suggesting that trace elements and stable noble gas isotopes reside within the same locations in diamond and track the same processes that are reflected in the trace element patterns. We cannot discern any temporal differences in these geochemical tracers, suggesting that the processes generating them have been occurring over at least the past 2.3?Ga. 3He/4He ratios decrease and 4He and 40Ar* contents increase with increasing age of peridotitic and some eclogitic diamonds, showing the importance of in-situ radiogenic 4He and 40Ar ingrowth by the decay of U-Th-Sm and K respectively. For most gem-quality monocrystalline diamonds, uncertainties in the 3He/4He evolution of the continental lithospheric mantle combined with large analytical uncertainties and possible spatial variability in U-Th-Sm concentrations limit our ability to provide estimates of diamond formation ages using 4He ingrowth. However, the limited observed 4He ingrowth (low U?+?Th/3He) together with a R/Ra value of 5.3 for peridotitic diamond K306 is comparable to the present-day sub-continental lithospheric mantle value and supports the young diamond formation age found by Re-Os dating of sulphides in the same diamond by Pearson et al. (1998). After correction for in-situ radiogenic 4He produced since diamond formation a large variation in 3He/4He remains in ?1?Ga old eclogitic diamonds that is suggested to result from the variable influence of subducted altered oceanic crust that has low 3He/4He. Hence, the 3He/4He isotope tracer supports an origin of the diamond-forming fluids from recycled oceanic crust for eclogitic diamonds, as indicated by other geochemical proxies.
Geochimica et Cosmochimica Acta, in press available 29p.
Africa, South Africa, Botswana
deposit - Koffiefontein, Letlhakane, Orapa, Finsch, De Beers Pool
Abstract: Ten individual gem-quality monocrystalline diamonds of known peridotite/eclogite paragenesis from Southern Africa (Koffiefontein, Letlhakane, Orapa) were studied for trace element concentrations and He and Ar abundances and isotopic compositions. In addition, two samples, consisting of pooled fragments of gem-quality peridotitic diamonds from Finsch and DeBeers Pool respectively, were analysed for noble gases. Previous studies (Richardson et al., 1984; Pearson et al., 1998; Gress et al., 2017; Timmerman et al., 2017) provided age constraints of 0.09, 1.0-1.1, 1.7, 2.3, and 3.2-3.4?Ga on mineral inclusions in the studied diamonds, allowing us to study trace elements and noble gases over 3 Gyr of geological time. Concentrations of trace elements in the diamonds are very low - a few hundred ppt to several tens of ppbs - and are likely dependent on the amount of sub-micron inclusions present. Trace element patterns and trace element/3He ratios of the studied monocrystalline diamonds are similar to those in fibrous diamonds, suggesting that trace elements and stable noble gas isotopes reside within the same locations in diamond and track the same processes that are reflected in the trace element patterns. We cannot discern any temporal differences in these geochemical tracers, suggesting that the processes generating them have been occurring over at least the past 2.3?Ga. 3He/4He ratios decrease and 4He and 40Ar* contents increase with increasing age of peridotitic and some eclogitic diamonds, showing the importance of in-situ radiogenic 4He and 40Ar ingrowth by the decay of U-Th-Sm and K respectively. For most gem-quality monocrystalline diamonds, uncertainties in the 3He/4He evolution of the continental lithospheric mantle combined with large analytical uncertainties and possible spatial variability in U-Th-Sm concentrations limit our ability to provide estimates of diamond formation ages using 4He ingrowth. However, the limited observed 4He ingrowth (low U?+?Th/3He) together with a R/Ra value of 5.3 for peridotitic diamond K306 is comparable to the present-day sub-continental lithospheric mantle value and supports the young diamond formation age found by Re-Os dating of sulphides in the same diamond by Pearson et al. (1998). After correction for in-situ radiogenic 4He produced since diamond formation a large variation in 3He/4He remains in ?1?Ga old eclogitic diamonds that is suggested to result from the variable influence of subducted altered oceanic crust that has low 3He/4He. Hence, the 3He/4He isotope tracer supports an origin of the diamond-forming fluids from recycled oceanic crust for eclogitic diamonds, as indicated by other geochemical proxies.
Abstract: The physical characteristics and impermeability of diamonds allow them to retain radiogenic 4He produced in-situ from radioactive decay of U, Th and Sm. This study investigates the U-Th/He systematics of fibrous diamonds and provides a first step in quantification of the uncertainties associated with determining the in-situ produced radiogenic 4He concentration. Factors determining the total amount of measured helium in a diamond are the initial trapped 4He, the in-situ produced radiogenic 4He, ?-implantation, ?-ejection, diffusion, and cosmogenic 3He production. Alpha implantation is negligible, and diffusion is slow, but the cosmogenic 3He component can be significant for alluvial diamonds as the recovery depth is unknown. Therefore, samples were grouped based on similar major and trace element compositions to determine possible genetically related samples. A correlation between the 4He and U-Th concentrations approximates the initial 4He concentration at the axis-intersect and age as the slope. In this study, the corrections were applied to eight fibrous cubic diamonds from the Democratic Republic of the Congo and two diamonds from the Jwaneng kimberlite in Botswana. A correlation exists between the 4He and U-Th concentrations of the group ZRC2, 3, and 6, and of the group CNG2, 3, and 4 and both correlations deviate significantly from a 71?Ma kimberlite eruption isochron. The U-Th/He dating method appears a promising new approach to date metasomatic fluid events that result in fibrous diamond formation and this is the first evidence that some fibrous diamonds can be formed 10s to 100s Myr before the kimberlite eruption.
Abstract: The fertility of the subcontinental lithospheric mantle as source for metal-rich magmas remains poorly understood. We report new major (EPMA), minor and trace element (LA-ICP-MS) results for olivine mantle xenocrysts sourced from the Jurassic age Jericho, Muskox and Voyageur kimberlites, western Nunavut in the Slave Craton, approximately 30 km north of the Lupin gold mine. Target elements include a suite of ore-forming elements that are unconventional for mantle petrology studies, but may represent important geochemical tracers for metal metasomatism. Using single-grain aluminum-in-olivine thermometry, formation temperatures for the olivine grains were calculated and projected on to a mantle geotherm to estimate PT conditions. The suite of xenocrysts corresponds to mantle sampling between 100-190 km depth. Their range in Mg# indicates that all 3 kimberlites sampled variably depleted mantle peridotite. The patterns of trace element enrichments found are consistent with those documented previously for mantle olivine xenocryst samples from the lithosphere below the Superior Craton in Kirkland Lake, Ontario. In both studies, some ore-forming elements were found to partition into mantle silicates more at the higher temperatures and pressure prevalent at the base of the lithospheric mantle, notably copper, with concentrations varying from ~ 1 ppm in shallow samples up to 11 ppm at the maximum depth sampled. Because the concentration of metals in melt-depleted lithospheric peridotite is expected to be low (< 20 ppm Cu), mantle silicates likely become a significant host for some ore elements at depth. Highly incompatible high field strength elements yield decreasing concentrations with depth, possibly the result of mantle metasomatic processes. Fluid metasomatized mantle peridotite domains are also inferred from olivine xenocrysts that yield unexpected trace element concentrations (ppb to ppm) for other highly incompatible ore-elements (e.g. As, Mo). We expect that some of these fluid-mobile and highly incompatible ore-elements represent trapped fluid and/or melt inclusions.
Abstract: The fertility of the subcontinental lithospheric mantle as source for metal-rich magmas remains poorly understood. We report new major (EPMA), minor and trace element (LA-ICP-MS) results for olivine mantle xenocrysts sourced from the Jurassic age Jericho, Muskox and Voyageur kimberlites, western Nunavut in the Slave Craton, approximately 30 km north of the Lupin gold mine. Target elements include a suite of ore-forming elements that are unconventional for mantle petrology studies, but may represent important geochemical tracers for metal metasomatism. Using single-grain aluminum-in-olivine thermometry, formation temperatures for the olivine grains were calculated and projected on to a mantle geotherm to estimate PT conditions. The suite of xenocrysts corresponds to mantle sampling between 100-190 km depth. Their range in Mg# indicates that all 3 kimberlites sampled variably depleted mantle peridotite. The patterns of trace element enrichments found are consistent with those documented previously for mantle olivine xenocryst samples from the lithosphere below the Superior Craton in Kirkland Lake, Ontario. In both studies, some ore-forming elements were found to partition into mantle silicates more at the higher temperatures and pressure prevalent at the base of the lithospheric mantle, notably copper, with concentrations varying from ~ 1 ppm in shallow samples up to 11 ppm at the maximum depth sampled. Because the concentration of metals in melt-depleted lithospheric peridotite is expected to be low (< 20 ppm Cu), mantle silicates likely become a significant host for some ore elements at depth. Highly incompatible high field strength elements yield decreasing concentrations with depth, possibly the result of mantle metasomatic processes. Fluid metasomatized mantle peridotite domains are also inferred from olivine xenocrysts that yield unexpected trace element concentrations (ppb to ppm) for other highly incompatible ore-elements (e.g. As, Mo). We expect that some of these fluid-mobile and highly incompatible ore-elements represent trapped fluid and/or melt inclusions.
Abstract: Subduction zones are an important way for crustal materials to enter deep parts of the Earth. Therefore, carbonatites in orogenic belt are of great significance in revealing deep carbon cycling pathways. To date, mantle-derived carbonatites have been identified in many orogenic belts, and their origin is considered to be related to subducted sediments. However, almost all orogenic carbonatites are composed of calcite, and their C isotopic compositions show typical mantle values, lacking any evidence of sedimentary origin. Here, we report decoupling of C and Sr isotopes between intimately associated dolomite and forsterite-calcite carbonatites from Caotan in the Qinling orogen, central China. The dolomite carbonatite is mainly composed of dolomite (plus minor apatite and magnetite), which has elevated ?13CPDB values (-3.1 to -3.6 ‰) and low 87Sr/86Sr ratios (0.7026-0.7042). The forsterite-calcite carbonatite consists of calcite (60-65 vol. %), forsterite and its replacement products (30-35 vol. %), and magnetite. The calcite shows mantle-like ?13CPDB (-6.2 to -7.2 ‰) but high initial 87Sr/86Sr values (0.7053-0.7076). Neodymium and Pb isotopic compositions are comparable in the two carbonatite types. The forsterite-calcite carbonatite is interpreted to have formed by metasomatic interaction of primary dolomitic melts with eclogite in thickened lower crust during collision of the North and South China cratons. The reaction resulted in decarbonation and depletion of the carbonatitic magma in 13C. Because of its initially low REE and Pb contents, the Nd-Pb isotopic signature of the primary dolomitic melt was preserved in the forsterite-calcite carbonatite. We propose that some orogenic calcite carbonatites may not be primary mantle-derived rocks and their mantle-like ?13CPDB values may be misleading.
Abstract: Nixonite (IMA 2018-133), ideally Na2Ti6O13, is a new mineral found within a heavily-metasomatized pyroxenite xenolith from the Darby kimberlite field, beneath the west central Rae Craton, Canada. It occurs as microcrystalline aggregates, 15 to 40 ?m in length. Nixonite is isostructural with jeppeite, K2Ti6O13, with a structure consisting of edge- and corner-shared titanium-centered octahedra that enclose alkali-metal ions. The Mohs hardness is estimated to be between 5 and 6 by comparison to jeppeite and the calculated density is 3.51(1) g/cm3. Electron microprobe wavelength-dispersive spectroscopic analysis (average of 6 points) yielded: Na2O 6.87, K2O 5.67 CaO 0.57, TiO2 84.99, V2O3 0.31, Cr2O3 0.04, MnO 0.01, Fe2O3 0.26, SrO 0.07, total 98.79 wt%. The empirical formula, based on 13 O atoms, is: (Na1.24K0.67Ca0.06)?1.97(Ti5.96V0.023Fe0.018)?6.00O13 with minor amounts of Cr and Mn. Nixonite is monoclinic, space group C2/m, with unit-cell parameters a = 15.3632(26) Å, b = 3.7782(7) Å, c = 9.1266(15) Å, ? = 99.35(15)º and V = 522.72(1) Å3, Z = 2. Based on the average of seven integrated multi-grain diffraction images, the strongest diffraction lines are [dobs in Å (I in %) (h k l)]: 3.02 (100) (3 1 0) , 3.66 (75) (1 1 0), 7.57 (73) (2 0 0), 6.31 (68) (2 0 -1), 2.96 (63) (3 1 -1), 2.96 (63) (2 0 -3) and 2.71 (62) (4 0 2). The five main Raman peaks of nixonite, in order of decreasing intensity, are at: 863, 280, 664, 135 and 113 cm-1. Nixonite is named after Peter H. Nixon, a renowned scientist in the field of kimberlites and mantle xenoliths. Nixonite occurs within a pyroxenite xenolith in a kimberlite, in association with rutile, priderite, perovskite, freudenbergite and ilmenite. This complex Na-K-Ti rich metasomatic mineral assemblage may have been produced by a fractionated Na-rich kimberlitic melt that infiltrated a mantle-derived garnet pyroxenite and reacted with rutile during kimberlite crystallization.
Geochimica et Cosmochimica Acta, in press available, 42p.
Canada, Northwest Territories
deposit -Diavik A154 N & S
Abstract: Kimberlite-borne granulite xenoliths provide rare insights into the age, chemical composition and tectonothermal evolution of the otherwise largely inaccessible deep cratonic crust. The formation and transformation of the lower continental crust (LCC) beneath the central Slave craton (Canada) is here illuminated using whole-rock trace-element and Sr-Nd isotope compositions of nine metabasaltic (MBG), one gabbroic (MGG) and two metasedimentary/hybrid (MSG) granulite xenoliths. On the one hand, published sulphide Re-Os and a few zircon U-Pb data indicate that at least a portion of the LCC beneath the central Slave craton has a Palaeoarchaean origin (?3.3?Ga), which apparently coincides with a period of juvenile crust and deep lithospheric mantle formation during plume impingement beneath the pre-existing cratonic nucleus. On the other hand, enrichment in Li, Sr, LREE, Pb and Th, but relative depletion in Ti, Hf and HREE, suggest formation of (picro)basaltic protoliths by partial melting of a subduction-modified garnet-bearing source, Crystallisation in the crust after fractionation of plagioclase is inidicated by their Sr and Eu negative anomalies, which are complementary to the positive anomalies in the MGG. Samarium-Nd isotopes in MBG and MGG show large scatter, but fall on Neo- or Mesoarchaean age arrays. These elemental systematics are suggested to fingerprint deserpentinisation fluids plus small amounts of sedimentary melt as the main contaminants of the mantle source, supporting the operation of at least regional and transient subduction at 3.3?Ga. Evidence for quasi-coeval plume impingement and subduction beneath the central Slave craton in the Mesoarchaean is reconcilable in a dynamic regime where vertical tectonics, though waning, was still active and plate interactions became increasingly important. Unradiogenic 87Sr/86Sr (down to 0.7017) is consistent with significant loss of Rb and probably other heat-producing elements (K, Th, U) plus H2O during Neoarchaean metamorphism, which helped to enhance LCC viscosity and stabilise the cratonic lithosphere.
Abstract: The genesis of Earth’s largest rare earth element (REE) deposit, Bayan Obo (China), has been intensely debated, in particular whether the host dolomite marble is of sedimentary or igneous origin. The protracted (Mesoproterozoic to Paleozoic) and intricate (magmatic to metasomatic) geological processes complicate geochemical interpretations. In this study, we present a comprehensive petrographic and in situ, high-spatial resolution Sr-Pb isotopic and geochemical investigation of the host dolomite from the Bayan Obo marble. Based on petrographic evidence, the dolomite marble is divided into three facies including coarse-grained (CM), fine-grained (FM), and heterogeneous marble (HM). All carbonates are ferroan dolomite with high SrO and MnO contents (>?0.15 wt.%), consistent with an igneous origin. Trace element compositions of these dolomites are highly variable both among and within individual samples, with CM dolomite displaying the strongest LREE enrichment. In situ 206Pb/204Pb and 207Pb/204Pb ratios of the dolomite are generally consistent with mantle values. However, initial 208Pb/204Pb ratios define a large range from 35.45 to 39.75, which may result from the incorporation of radiogenic Pb released from decomposition of monazite and/or bastnäsite during Early Paleozoic metasomatism. Moreover, in situ Sr isotope compositions of dolomite indicate a large range (87Sr/86Sr?=?0.70292-0.71363). CM dolomite is characterized by a relatively consistent, unradiogenic Sr isotope composition (87Sr/86Sr?=?0.70295-0.70314), which is typical for Mesoproterozoic mantle. The variation of 87Sr/86Sr ratios together with radiogenic 206Pb/204Pb signatures for dolomite within FM and HM possibly represents recrystallization during Early Paleozoic metasomatism with the contribution of radiogenic Sr and Pb from surrounding host rocks. Therefore, our in situ geochemical data support a Mesoproterozoic igneous origin for the ore-bearing dolomite marble in the Bayan Obo deposit, which subsequently underwent intensive metasomatism during the Early Paleozoic.
Abstract: The late Jurassic Masontown dyke in Fayette County, SW Pennsylvania, preserves abundant rounded, mm to cm-diameter masses of olivine and serpentine cemented together in serpentine-rich kimberlite groundmass. Each mass is interpreted to be a partially serpentinized olivine xenocryst or peridotite xenocryst. Each rounded clast is jacketed by a distinct rim of serpentine; probably originally olivine. The (1) ubiquitous roundness of clasts and (2) the presence of distinct serpentine jackets around each clast, supports emplacement of the dyke by a 'kimberlite factory' (Brett et al., 2015). Due to the paucity of available samples, we have used non-destructive imaging by computed tomography (CT) at the National Energy Technology Lab in Morgantown, WV, to construct 3D models of the internal structure of hand samples loaned from the Smithsonian Institute's Museum of Natural History. MicroCT (1-3 micron resolution) and industrial CT (~15 microns resolution) serial scans processed in ImageJ and Blob3D allow for 3D characterizations of individual clasts, including their shape factors (sphericity, roughness, etc.) and sizes (i.e. crystal size distributions).
Abstract: Monocrystalline type Ia diamonds with octahedral growth morphology prevail among lithospheric diamonds, including precious stones. Unlike less common ‘fibrous’ diamonds that grew from alkali-rich carbonate-bearing melts and fluids, the growth medium of ‘monocrystalline’ type Ia diamonds remains debatable. Here we report the first finding of an optically visible (~30??m in size) carbonate inclusion in the center of a gem type Ia octahedral diamond from the Sytykanskaya kimberlite pipe, Yakutia. We found that the inclusion consists of submicron size carbonate phases represented by K2Ca(CO3)2 bütschliite (~15?vol%), Na2Mg(CO3)2 eitelite (~5?vol%), and dolomite (~80?vol%). Although neither bütschliite nor eitelite can coexist with dolomite under mantle P-T conditions, these phases readily appear all together in the quenched products of carbonatite melt under mantle pressures. Thus, at the moment of capture, the inclusion material was a carbonatite melt with the following composition 10(K0.75Na0.25)2CO3?90(Ca0.57Mg0.43)CO3. The content of alkali carbonates at the level of 10?mol% indicates that the melt was formed at a temperature of ?1300?°C. The high K/Na and Ca/(Ca?+?Mg) ratios in this melt indicate its derivation by partial melting of recycled marine sediments (pelites). Considering an age of the last subduction event beneath the Siberian craton, our new finding implies that subducting slabs drag carbonated material of the continental crust beneath ancient cratons, where it experiences partial melting to form a potassic dolomitic melt responsible for the formation of most diamonds, since the Late Archean.
Abstract: International Symposium on Deep Earth Exploration and Practices Beijing, China -October24-26, 2018The protolithnatureof diamondiferous metamorphic rocks of the Kokchetav MassifVladislav Shatsky1,2,3, Emil Jagoutz4, Olga Kozmenko1, Alexey Ragozin1,3, Sergei Skuzovatov2and Nikolai Sobolev1,31Sobolev Institute of Geology and Mineralogy SB RAS, Novosibirsk, 630090, Russia, [email protected] Institute of Geochemistry SB RAS, Irkutsk, Russia3Novosibirsk State University, Novosibirsk, Russia4Max Planck Institute for Chemistry, Mainz, GermanyUltra-high-pressure diamondiferous rocks (UHP) of the Kokchetav subduction-collision zone are considered as an idealobject for studying the mobility of elements insubduction zones of the continental type. The compositional diversity of metasedimentary rocks subjected to UHP metamorphism makes it difficult to establish the nature of their protoliths. This, in turn, complicates estimatesof the degree of depletionof the UHP metamorphic rocks relative to the protoliths.To clarify the nature of protholiths of the Kokchetav diamondiferous rocks we studied the geochemical features and Sm-Nd isotopic composition of diamondiferous calc-silicate, garnet-pyroxene rocks, high-alumina metapelitesand barren granite-gneisses.The nine samples of the Kumdy Kol mocrodiamond deposit (one granite-gneiss, 4-calc-silicate rocks, 3-garnet-pyroxenite) yielded aSm-Nd whole-rockisochronageof 1052±44 Ma. This age is close to the age of formation of the granitic gneiss basement of the Kokchetav massif (1.2-1.05 Ga) (Glorie et al., 2015). Therefore, we assume that the protoliths of these rocks were basementrocks. In this interpretation, their geochemical features may not be directly related to the processes of ultrahigh-pressure metamorphism.At the same time, the high-alumina rocks of the Barchinsky area are depleted todifferent degreeswithrespect to LREE and K yieldeda whole-rockisochron with an age of 509 ± 32 Ma, which suggests partial melting of these rocks duringthe exhumation stage.It was previously assumed that metasedimentary rocks of the Kokchetav microcontinent are the protoliths of diamondiferous rocks (Buslov et al., 2015). However, this contradicts with Sm-Nd isotopic data for metasedimentary rocks of quartzite-schist sequences of the Kokchetav microcontinent (Kovach et al., 2017). The metasedimentary rocks of the Sharyk Formation are characterized by variations in the ?Nd(t)from +4.1 to -3.3 and intNd(DM)from 1.9 to 1.25 Ga, whereasin the UHP metamorphic rocks ?Nd(t)varies from -7.6 to -13.2, and the model ages range from 2.7 to 2.3 Ga. These data clearly indicate that the metasedimentary rocks of the Kokchetav massif could not be the protolith of the ultrahigh-pressure rocks.
Abstract: The article describes the petrography and mineralogy of xenoliths ilmenite-phlogopite containing deformed and granular peridotites from the Udachnaya-Eastern pipe. The age of pholopite porphyroclast from the studied deformed xenoliths matches with age of Phl megacryst and itself hosted kimberlites from Udachnaya pipe indicating the following processes closed in time: (1) crystallization of the low-Cr megacryst association; (2) deformation of rocks on the mantle lithosphere-asthenosphere border during the kimberlite-forming cycle; (3) formation of protokimberlite melts.
Abstract: This study reports the combined major, minor and trace element compositions, and stable (C, O), radiogenic (Nd, Pb, and Sr) isotopic compositions, and first ?11B isotopic data for the Fir, Felix, Gum, and Howard Creek carbonatites from the Blue River Region, British Columbia (Canada). These sill-like occurrences were intruded into Late Proterozoic strata during rifting and extensional episodes during the Late Cambrian and Devonian -Mississippian, and subsequently deformed and metamorphosed to amphibolite grade in relation to a collisional-type tectonic environment. The carbonatites at Fir, Gum, and Felix contain both calcite and dolomite, whereas the carbonatite at Howard Creek contains only calcite. The dolomite compositions reported here are consistent with those experimentally determined by direct partial melting of metasomatized peridotitic mantle. The combined major and trace element compositions and ?13CPDB (?5.37 to ?4.85‰) and ?18OSMOW (9.14 to 9.62‰) values for all the samples investigated are consistent with those for primary igneous carbonate and support their mantle origin. However, these signatures cannot be attributed to closed system melt differentiation from a single parental melt. The initial Nd, Pb, and Sr isotopic ratios are highly variable and suggest generation from multiple, small degree parental melts derived from a heterogeneous mantle source. The ?11B values for carbonates from Felix, Gum, and Howard Creek vary between ?8.67 and ?6.36‰, and overlap the range for asthenospheric mantle (?7.1?±?0.9‰), whereas two samples from Fir yield heavier values of ?3.98 and ?2.47‰. The latter indicate the presence of recycled crustal carbon in their mantle source region, which is consistent with those for young (<300?Ma) carbonatites worldwide. The radiogenic and B isotope results for the Blue River carbonatites are compared to those from contrasting, anorogenic tectonic settings at Chipman Lake, Fen, and Jacupiranga, and indicate that similar upper mantle sources are being tapped for carbonatite melt generation. The pristine, mantle-like ?11B values reported here for the Blue River carbonatites clearly demonstrate that this isotope system is robust and was not perturbed by post-solidification tectono-metamorphic events. This observation indicates that B isotope signatures are a valuable tool for deciphering the nature of the upper mantle sources for carbonates of igneous origin.
Geochimica et Cosmochimica Acta, in press available doi.org/10.1016 / j.gca.2019.06.041 36p.
Africa, Tanzania, Canada, East Africa, Europe, Germany, Greenland
deposit - Oldoinyo Lengai
Abstract: To investigate the behaviour of Ba isotopes during carbonatite petrogenesis and to explore the possibility of using carbonatites to constrain the Ba isotopic composition of the mantle, we report high-precision Ba isotopic analyses of: (1) carbonatites and associated silicate rocks from the only active carbonatite volcano, Oldoinyo Lengai, Tanzania, and (2) Archean to Cenozoic carbonatites from Canada, East Africa, Germany and Greenland. Carbonatites and associated phonolites and nephelinites from Oldoinyo Lengai have similar ?137/134Ba values that range from +0.01 to +0.03‰, indicating that Ba isotope fractionation during carbonatite petrogenesis is negligible. The limited variation in ?137/134Ba values from ?0.03 to +0.09‰ for most carbonatite samples suggests that their mantle sources have a relatively homogeneous Ba isotopic composition. Based on the carbonatites investigated in this work, the average ?137/134Ba value of their mantle sources is estimated to be +0.04?±?0.06‰ (2SD, n?=?16), which is similar to the average value of +0.05?±?0.06‰ for mid-ocean ridge basalts. The lower ?137/134Ba value of ?0.08‰ in a Canadian sample and higher ?137/134Ba values of +0.14‰ and?+?0.23‰ in two Greenland samples suggest local mantle isotopic heterogeneity that may reflect the incorporation of recycled crustal materials in their sources.
Abstract: The microinclusions in cuboid diamonds from Ebelyakh River deposits (northeastern Siberian craton) have been investigated by FIB/TEM techniques. It was found that these microinclusions have multiphase associations, containing silicates, oxides, carbonates, halides, sulfides, graphite, and fluid phases. The bulk chemical composition of the microinclusions indicates two contrasting growth media: Mg-rich carbonatitic and Al-rich silicic. Each media has their own specific set of daughter phases. Carbonatitic microinclusions are characterized by the presence of dolomite, phlogopite, apatite, Mg, Fe-oxide, KCl, rutile, magnetite, Fe-sulfides, and hydrous fluid phases. Silicic microinclusions are composed mainly of free SiO2 phase (quartz), high-Si mica (phengite), Al-silicate (paragonite), F-apatite, Ca-carbonates enriched with Sr and Ba, Fe-sulfides, and hydrous fluid phases. These associations resulted from the cooling of diamond-forming carbonatitic and silicic fluids/melts preserved in microinclusions in cuboid diamonds during their ascent to the surface. The observed compositional variations indicate different origins and evolutions of these fluids/melts.
Abstract: In the central-northern portion of Archon lithospheric nucleus of the Rio de la Plata craton, the so-called rift/graben of Asunción was positioned; structure that would have formed thanks to a crustal thinning previously caused by the impact of a meteorite that forms the San Miguel impact cráter. The mega-impact structure is located immediately to the south of the Asunción rift/graben. Within the central segment E-W of the rift/graben and in association with other volcanic, sub-volcanic to plutonic rocks (potasic to ultra-potasic type Roman Province and lamproitic) of around 130-125 Ma., the picritic rock pipe with lamprofidic texture Ymi-1 occurs. Pipe that was positioned in the heavily depressed area (depths of up to -3000 meters) of the rift/graben. The Ymi-1 pipe would have been installed following faults, apparently very powerful, of the aforementioned distensive structure. Rocks of a plug and a dike exposed in the pipe Ymi-1 show that it is a strongly porphyritic rock with tendencies of lamprophidic texture formed by micro-feno-mega-crystals of forsteritic olivine (>10 to 30% modal); pheno-mega-crystals of titanium aluminosus diopside and chromite ((Mg-chromite poor in Ti and Mg-Ti chromite) micro-phenocrysts; they are supported by an inter-granular matrix formed by aluminosus diopside, Al-Ti-phlogopite-biotite, Mg-Ti-magnetite, amphiboles (Hornblends, eckernmanite together with some other potassium to sodic titaniferous amphiboles) accompanied by sanidine, analcime and traces of plagioclase (poor in An molecules). The mineral chemistry of spinels, phlogopites-biotites and diopsids are strongly compatible with mineral chemistry known in calc-alkaline lamprophyres. The rock chemistry of one available dyke is also compatible with the chemistry of calc-alkaline lamprophyres (SiO2 49.8%, with K2O/Na2O> 1, MgO 12%, Ni 298-ppm, Cr 904-ppm, La-76 ppm, Lu 0.15-ppm, TiO2 1.27%; CaO 8.59% and ratios of Sr87 / Sr86 = 0.707238 and 143Nd / 144Nd = 0.51196).Ymi-1 a calc-alkaline picritic lamprophyre pipe where the study of the chromite (50-57 % Cr2O3) type and frosting-tourmaline ("dravites"), obtained in rock and in heavy mineral concentrates (in vulcano-epi-clastic sediments and in stream sediments -collected in its bed) suggest that it would be a diamond-bearing lamprophyre. The presence of diamonds was confirmed (by X-rays and other methods) in the Ymi-1 pipe. 1D S-wave seismic profile of continental data, for the pipe Ymi-1 site, suggests a geothermal gradient between 38.5 to 39 mw/m2. Data that make the Ymi-1 calc-alkaline lamprophyre an attractive target for an eventual diamonds deposit.
Abstract: New findings of silicate-melt inclusions in two alluvial diamonds (from the Kholomolokh placer, northeastern Siberian Platform) are reported. Both diamonds exhibit a high degree of N aggregation state (60-70% B) suggesting their long residence in the mantle. Raman spectral analysis revealed that the composite inclusions consist of clinopyroxene and silicate glass. Hopper crystals of clinopyroxene were observed using scanning electron microscopy and energy-dispersive spectroscopic analyses; these are different in composition from the omphacite inclusions that co-exist in the same diamonds. The glasses in these inclusions contain relatively high SiO2, Al2O3, Na2O and, K2O. These composite inclusions are primary melt that partially crystallised at the cooling stage. Hopper crystals of clinopyroxene imply rapid cooling rates, likely related to the uplift of crystals in the kimberlite melt. The reconstructed composition of such primary melts suggests that they were formed as the product of metasomatised mantle. One of the most likely source of melts/fluids metasomatising the mantle could be a subducted slab.
Abstract: To clarify the tectonic-thermal evolution of the Anabar tectonic province in the central Siberian Craton, we performed an isotope-geochemical study of 20 xenoliths from the Udachnaya, Zarnitsa, and Komsomolskaya kimberlite pipes to represent different crustal levels. Most mafic granulites have Proterozoic Nd model ages and geochemical characteristics close to those of intraplate basalts, whereas some mafic and intermediate granulites with Archean model ages exhibit geochemical features of supra-subduction ophiolitic basalts. Analysis of U-Pb ages and hafnium isotopic composition of zircon indicates that the main tectonic-thermal events modified the crust at 2.7 and 1.9-1.8?Ga, which is consistent with ages of mantle depletion events from previous studies. All zircons have Archean Hf model ages (3.2?Ga). Overall, thermal events with ages of 2.9-2.8, 2.7, 2.4, 1.97 and 1.8?Ga have remarkable influence on the studied zircons. Tectono-thermal events at 2.4 1.97, 1.9 and 1.8?Ga with no addition of juvenile material are recorded by zircons from xenoliths of mafic and intermediate granulites and metadiorites. A compilation of isotope-geochemical data demonstrates that instead of age-stratified, the crust of the Anabar tectonic province consists of variably reworked Paleoarchean rocks and juvenile Proterozoic rocks at all crustal levels. Hence the crust and mantle of the Siberian Craton has been coupled since the Paleoarchean.
Abstract: To clarify the tectonic-thermal evolution of the Anabar tectonic province in the central Siberian Craton, we performed an isotope-geochemical study of 20 xenoliths from the Udachnaya, Zarnitsa, and Komsomolskaya kimberlite pipes to represent different crustal levels. Most mafic granulites have Proterozoic Nd model ages and geochemical characteristics close to those of intraplate basalts, whereas some mafic and intermediate granulites with Archean model ages exhibit geochemical features of supra-subduction ophiolitic basalts. Analysis of U-Pb ages and hafnium isotopic composition of zircon indicates that the main tectonic-thermal events modified the crust at 2.7 and 1.9-1.8?Ga, which is consistent with ages of mantle depletion events from previous studies. All zircons have Archean Hf model ages (3.2?Ga). Overall, thermal events with ages of 2.9-2.8, 2.7, 2.4, 1.97 and 1.8?Ga have remarkable influence on the studied zircons. Tectono-thermal events at 2.4 1.97, 1.9 and 1.8?Ga with no addition of juvenile material are recorded by zircons from xenoliths of mafic and intermediate granulites and metadiorites. A compilation of isotope-geochemical data demonstrates that instead of age-stratified, the crust of the Anabar tectonic province consists of variably reworked Paleoarchean rocks and juvenile Proterozoic rocks at all crustal levels. Hence the crust and mantle of the Siberian Craton has been coupled since the Paleoarchean.
Abstract: To clarify the tectonic-thermal evolution of the Anabar tectonic province in the central Siberian Craton, we performed an isotope-geochemical study of 20 xenoliths from the Udachnaya, Zarnitsa, and Komsomolskaya kimberlite pipes to represent different crustal levels. Most mafic granulites have Proterozoic Nd model ages and geochemical characteristics close to those of intraplate basalts, whereas some mafic and intermediate granulites with Archean model ages exhibit geochemical features of supra-subduction ophiolitic basalts. Analysis of U-Pb ages and hafnium isotopic composition of zircon indicates that the main tectonic-thermal events modified the crust at 2.7 and 1.9-1.8?Ga, which is consistent with ages of mantle depletion events from previous studies. All zircons have Archean Hf model ages (3.2?Ga). Overall, thermal events with ages of 2.9-2.8, 2.7, 2.4, 1.97 and 1.8?Ga have remarkable influence on the studied zircons. Tectono-thermal events at 2.4 1.97, 1.9 and 1.8?Ga with no addition of juvenile material are recorded by zircons from xenoliths of mafic and intermediate granulites and metadiorites. A compilation of isotope-geochemical data demonstrates that instead of age-stratified, the crust of the Anabar tectonic province consists of variably reworked Paleoarchean rocks and juvenile Proterozoic rocks at all crustal levels. Hence the crust and mantle of the Siberian Craton has been coupled since the Paleoarchean.
Abstract: Accurately dating the formation and modification of Earth’s sub-cratonic mantle still faces many challenges, primarily due to the long and complex history of depletion and subsequent metasomatism of this reservoir. In an attempt to improve this, we carried out the first study on peridotites from the Kaapvaal craton (Finsch Mine) that integrates results from Re-Os, Lu-Hf, Sm-Nd and Sr-isotope systems together with analyses of major-, trace- and platinum-group elements. The Finsch peridotites are well-suited for such a study because certain compositional features reflect they were highly depleted residues of shallow melting (1.5?GPa) at ambient Archean mantle temperatures. Yet, many of them have overabundant orthopyroxene, garnet and clinopyroxene compared to expected modal amounts for residues from partial melting. Finsch peridotites exhibit a wide range of rhenium depletion ages (TRD) from present day to 2.7?Ga, with a prominent mode at 2.5?Ga. This age overlaps well with a Lu-Hf isochron of 2.64?Ga (?Hf (t)?=?+26) which records silico-carbonatitic metasomatism of the refractory residues. This late Archean metasomatism is manifested by positive correlations of Pt/Ir and Pd/Ir with 187Os/188Os ratios and good correlations of modal amounts of silicates, especially garnet, with Os isotope ratios. These correlations suggest that the Highly Siderophile Elements (HSE) and incompatible element reenrichment and modal metasomatism result from one single major metasomatic event at late Archean. Our detailed study of Finsch peridotites highlights the importance of using multiple isotopic systems, to constrain the ages of events defining the evolution of lithospheric mantle. The Re-Os isotope system is very effective in documenting the presence of Archean lithosphere, but only the oldest TRD ages may accurately date or closely approach the age of the last major partial melting event. For a meaningful interpretation of the Re-Os isotope systematics the data must be combined with HSE patterns, trace-element compositions and ideally other isotopic systems, e.g. Lu-Hf. This is highlighted by the widespread evidence in Finsch peridotites of Pt, Pd and Re enrichment through significant Base Metal Sulfide (BMS) addition (mainly in the range of 0.002-0.08?wt%) that systematically shifts the mode of TRD model ages to younger ages.
Abstract: The powerpoint of the presentation made by Wiehan Smit at the SAIMM July 2019 Grade Control School has been made available by the author as a pdf file.
Abstract: He-Ne-Ar compositions were determined in diamonds from the Argyle lamproite, Western Australia, to assess whether subducted material affects the noble gas budget and composition of stable old sub-continental lithospheric mantle (SCLM). Twenty diamonds (both peridotitic and eclogitic) were characterized for their carbon isotopic compositions and N abundance and aggregation from which 10 eclogitic growth zones and 5 peridotitic growth zones were analysed for their He-Ne-Ar compositions. The eclogitic diamonds have ?13C values of ?4.7 to ?16.6‰ indicating a subduction signature, whereas the peridotitic diamonds have mantle-like compositions of ?4.0 to ?7.8‰. Mantle residence temperatures based on N-in-diamond thermometry showed that the eclogitic diamonds were mainly formed at 1260-1270?°C or above 1300?°C near the base of the lithosphere, whereas the peridotitic diamonds generally formed at lower temperatures (mostly 1135-1230?°C). A noble gas subduction signature is present to various extents in the eclogitic diamonds and is inferred from a hyperbolic mixing relationship between R/Ra and 4He and ?13C values concentrations with a predominance of low R/Ra values (<0.5; R/Ra?=?3He/4Hesample/3He/4Heair). In addition, low 40Ar/4He and 40Ar/36Ar ratios, high nucleogenic 21Ne/4He and low 3He/22Ne ratios are characteristic of subducted material and were found in the eclogitic diamonds. The peridotitic diamonds show generally higher R/Ra values (median 1.1?±?1.1) and lower 4He/40Ar ratios compared to eclogitic diamonds (median 0.1?±?0.8 R/Ra; with 7/10 samples having an average of 0.13?±?0.14 R/Ra). The studied peridotitic diamond growth zones showed a negative correlation between R/Ra and 4He concentrations over 2 orders of magnitude and limited variation in 3He, that can be largely explained by radiogenic 4He ingrowth. At low 4He concentrations the R/Ra value is around 2.8 for both paragenesis of diamonds and is significantly lower than present-day SCLM values, suggesting (1) a more radiogenic helium isotope composition beneath the Halls Creek Orogen than those for typical SCLM from other cratons and/or (2) that the peridotitic diamonds are formed from fluids that also had a subduction input. The high mantle residence temperature and low R/Ra value in the core and low temperature and higher R/Ra value in the rim of a single peridotitic diamond indicate multiple growth events and that part of the lherzolitic diamond population may be genetically related to the eclogitic diamonds. Combining the diamond mantle residence temperatures with noble gas compositions shows that noble gas subduction signatures are present at the base of the lithosphere below 180?km depth beneath Argyle and that fluid migration and interaction with the SCLM occurred over scales of at least 15?km, between 180 and 165?km depth.
Abstract: The chemical compositions of garnets from a megacryst association of the Mir kimberlite pipe have been studied. By petrogenic elements, the garnet megacrysts can be classified as high-Ti and low-Cr pyrope. The megacryst TiO2 contents of the Mir pipe correlate inversely with the MgO and Cr2O3 contents. Modeling of the composition of garnets through a fractional crystallization process showed that the most suitable composition of the melts parental for the garnets of the megacryst association is picrite. The composition of garnets crystallized from the kimberlite does not correspond to the composition of the natural garnets from the Mir pipe. The kimberlites contain less Ti, Zr, Y, and HREEs, but are more enriched with strongly incompatible elements (LREEs, Th, U, Nb, Ta, and Ba) than the model composition of the melt suitable for crystallization of the garnet megacrysts.
Abstract: The Earth’s only active natrocarbonatite volcanism at Oldoinyo Lengai suggests that natrocarbonatite melts are formed through a unique geological process. In the East African Rift, the Kerimasi is a neighbor of Oldoinyo Lengai and also contains nephelinites hosting melt and fluid inclusions, which preserve the magmatic processes associated with formation of natrocarbonatite melts. In this study, we present evidence for the presence of coexisting nephelinite melt, fluorine-rich carbonate melt and alkali carbonate fluid. Compositions of these phases differ from the composition of Oldoinyo Lengai natrocarbonatites, therefore, it is not likely that natrocarbonatites formed directly from one of these phases. However, mixing of the outgassing alkali carbonate fluid and the fluorine-rich carbonate melt can yield natrocarbonatite compositions at temperatures close to subsolidus temperatures of the nephelinite (~630 oC). Moreover, the high halogen (F+Cl) content (6-16 wt%) in the carbonate melt precludes saturation of calcite (i.e., formation of calciocarbonatite) and maintains the carbonate melt in the liquid state with 28-41 wt% CaO at temperatures ?600 oC. Our study suggests that alkali carbonate fluids and melts could have commonly formed in the geological past, but it is unlikely they precipitated calcite that facilitates fossilization. Instead, alkali carbonates precipitated which were not preserved in the fossil nephelinite rocks. Thus, alkali carbonate fluids and melts have been so far unaccounted in the geological record because of the lack of former detailed inclusion studies. In addition, the observed low H2O (<4 wt%) content of the alkali carbonate fluid phase shows that a H2O-rich environment is not required for the generation of natrocarbonatites as suggested by previous models. Our model [1] is consistent with the observation that natrocarbonatites are associated with nephelinite rocks [2], as occurs at Oldoinyo Lengai, rather than with calciocarbonatites.
Geochimica et Cosmochimica Acta, in press available 49p. Pdf
Africa, South Africa
deposit - Benfontein
Abstract: Olivine chemistry has been widely used to track the petrogenesis of mafic and ultramafic magmas from their mantle source to eruption at the surface. A major challenge in these studies is deciphering crystal growth versus diffusion controlled zoning. Here we report a multi-element approach using high-precision electron microprobe techniques to evaluate crystal growth versus diffusion in kimberlitic olivine from the Benfontein kimberlite, South Africa. These results have implications for both the petrogenesis of kimberlite magmas and the understanding of crystal growth and diffusion-based zoning in igneous olivine in general. The Benfontein olivine contain multiple phosphorous (P)-rich and P-poor zones. Core zones are characterized by homogenous low-P (<78?ppm) concentrations, consistent with xenocrystic origins. Gradational changes in Fo, Ni, Cr and other minor/trace elements at core-margins are similarly characterized by constant low-P concentrations that are indistinguishable from the central regions of the core. Olivine P-maps effectively outline the original xenocryst core, whereas gradational margins are interpreted as diffusion controlled zones related to early-stage equilibration of xenocrystic olivine with proto-/kimberlite melt. Multiple P-poor (100-150?ppm) and P-rich (200-450?ppm) concentric, oscillatory zones with inclusions of kimberlitic oxide phases are observed surrounding the low-P xenocrystic cores. Oxide phases change from chromite in the inner zones to ilmenite in the intermediate zones to magnetite-rich spinel in the outer zones of the olivine. The P-zoning corresponds with changes in Fo content implying that stages of crystal growth was preserved by both fast and slow diffusing elements rather than diffusion processes. Elements compatible with olivine (±chromite) crystallization (i.e., Ni and Cr) display a constant decrease across all zones, suggesting that magma mixing is unlikely a controlling process for P-zoning. We interpret P-rich zones to result from stages of solute trapping related of rapid disequilibrium growth driven by extrinsic factors such as changes in pressure-temperature during kimberlite evolution. In contrast, P-poor zones represent stages of equilibrium crystal growth. The outer olivine zones are characterized by an increase in Fo contents up to Fo96, and in conjunction with a change to more Fe3+-rich oxides, suggest late stage increase in fO2. Correlated Fo and P changes in the Benfontein olivine suggest that major element zonation represents an example where crystal growth-induced Fo zoning has been preserved in olivine. Furthermore, P-rich olivine zones preserve evidence for concentric growth rather than common dendritic structures seen in other occurrences. These results have implications for understanding the effect of magma dynamics and changes in pressure-temperature-fO2 conditions on olivine growth in igneous rocks.
Abstract: Three groups of diamond crystals that differ in morphology, photoluminescence, infrared absorption, and thermal history were discovered in the Lomonosov deposit. The first group crystals are mostly octahedrons with minor signs of dissolution and a large share of nitrogen in the form of B defects. The crystals of the second type are strongly resorbed dodecahedroids with a small share of B defects. The third group consists of crystals with low-temperature ? defects; they are cuboids that are often without traces of resorption, and tetrahexahedroids. These patterns indicate the polygenicity of the diamond in the Lomonosov deposit.
Abstract: Monocrystalline type Ia diamonds with octahedral growth morphology prevail among lithospheric diamonds, including precious stones. Unlike less common ‘fibrous’ diamonds that grew from alkali-rich carbonate-bearing melts and fluids, the growth medium of ‘monocrystalline’ type Ia diamonds remains debatable. Here we report the first finding of an optically visible (~30??m in size) carbonate inclusion in the center of a gem type Ia octahedral diamond from the Sytykanskaya kimberlite pipe, Yakutia. We found that the inclusion consists of submicron size carbonate phases represented by K2Ca(CO3)2 bütschliite (~15?vol%), Na2Mg(CO3)2 eitelite (~5?vol%), and dolomite (~80?vol%). Although neither bütschliite nor eitelite can coexist with dolomite under mantle P-T conditions, these phases readily appear all together in the quenched products of carbonatite melt under mantle pressures. Thus, at the moment of capture, the inclusion material was a carbonatite melt with the following composition 10(K0.75Na0.25)2CO3?90(Ca0.57Mg0.43)CO3. The content of alkali carbonates at the level of 10?mol% indicates that the melt was formed at a temperature of ?1300?°C. The high K/Na and Ca/(Ca?+?Mg) ratios in this melt indicate its derivation by partial melting of recycled marine sediments (pelites). Considering an age of the last subduction event beneath the Siberian craton, our new finding implies that subducting slabs drag carbonated material of the continental crust beneath ancient cratons, where it experiences partial melting to form a potassic dolomitic melt responsible for the formation of most diamonds, since the Late Archean.
Abstract: Contamination of carbonatites with crustal or cogenetic intrusive rocks is generally not considered to play an important role during carbonatite magmatism, because carbonatitic melts have low densities and viscosities, enabling them to rapidly ascend. Potential contamination by silicate rocks in carbonatites cannot easily be detected by means of radiogenic isotope data (such as Sr, Nd and Pb isotope data) as carbonatites often show high concentrations of these elements and their isotope systems are thereby “buffered” against contamination with silicate rocks. Textural, mineralogical and geochemical observations in carbonatites from the Kaiserstuhl (Germany) provide evidence for the interaction of carbonatitic magma with previously emplaced nosean syenites. This caused replacement of alkali feldspar by haüyne and recrystallization of garnet and clinopyroxene in the xenoliths, which released larger amounts of K, Al, Si and Fe. As a result, blackwall-like mica seams around the xenoliths formed and and compositionally distinct mica and clinopyroxene crystallized in the surrounding carbonatite. Moreover, the local increase of silica activity during contamination enabled strong REE enrichment in apatite via a coupled substitution involving Si, which demonstrates the potential influence of Si contamination on REE mineralization in carbonatites. We further suggest that the presence and composition of clinopyroxene and mica in carbonatites may be useful indicators for contamination processes during their emplacement. Mass-balance calculations based on experimental constraints for the solubility of Al and Si in carbonatitic magmas suggest that only minor amounts of mica can form from carbonatitic melt. Therefore, larger amounts of mica and mica-dominated lithologies (glimmerites) as observed in many carbonatite complexes suggest that some Si and Al in carbonatites may be sourced from surrounding host rocks. We hypothesize that assimilation and contamination processes in carbonatites may be the rule rather than an exception.
Abstract: Carbonatites are rare magmas containing almost no silica; their igneous counterparts represent the main rare earth element deposits inoperation. No consensus exists on their origin, genesis and evolution. Oldoinyo Lengai (Tanzania) is the only active carbonatite volcano, but the alkali-rich natrocarbonatites it erupts are unique among the >500 reported fossil carbonatite occurrences. Here, we use threephase melt inclusions hosted in minerals from cognate cumulates (clinopyroxene, nepheline, Ti-garnet, interstitial melt)— which sampled the active Oldoinyo Lengai magma chamber during the 2007-08 sub-Plinian explosive eruption—to track the carbonatite presence within the plumbing system, and to eventually quantify its composition at depth. We show that although natrocarbonatites are emitted at the Oldoinyo Lengai summit, more classical calciocarbonatites are present at magma chamber depth (~3.5 kbar, 1050 to 900°C), which is consistent with the model of rare natrocarbonatites deriving from calciocarbonatites by further magma differentiation. We also show that those calciocarbonatites are not isolated but rather conjugated with alkali-rich silica melt suggesting a joint evolution. We eventually present the first direct measurements of major and trace element partition coefficients between natural coexisting carbonate and silicate melts. Partitioning behaviour and recent experiments support our conclusion that natrocarbonatites derive from calciocarbonatites by fractionating Ca-rich, Na-poor phases. As natrocarbonatites are highly unstable at surface conditions, they were likely erupted but not preserved in association with fossil calciocarbonatites worldwide. Oldoinyo Lengai can then be considered as representative of other carbonatite systems, and provide us with the unique opportunity to observe the plumbing system architecture, and to constrain the protracted differentiation path of a carbonatite system.
Phd. Thesis University of Alberta, 147p. See note on front page - see U of A search strategy on cover page
Africa, Botswana
deposit - Karowe
Abstract: This study presents the first comprehensive data on the recently developed Karowe diamond mine from the Orapa kimberlite cluster, which hosts mines such as Orapa, Damtshaa, and Letlhakane. The objectives of the study were to establish the compositional characteristics of the lithospheric mantle beneath the Karowe mine at the time of kimberlite eruption by studying the major- and trace-element characteristics of 24 mantle xenoliths and 106 clinopyroxene xenocrysts. In addition, the possible diamond sources beneath Karowe were evaluated through examination of major- and trace-element compositions of mineral inclusions in 120 diamonds. Finally, the physical characteristics of the diamonds themselves as well as their total nitrogen contents and carbon isotope compositions were investigated.The mantle xenoliths are predominantly melt-depleted garnet-free spinel peridotites (n = 14), with a small proportion of pervasively refertilised garnet-spinel lherzolites (n = 4), and variably metasomatised garnet-bearing pyroxenites (n = 3). The remaining three xenoliths are a garnet lherzolite, an eclogite, and a megacrystic olivine. The mineralogical evidence indicates that all these come from relatively low-pressure regions of the mantle outside of the diamond stability field. The predominant spinel lherzolites are characterised by coarse-grained and granolublastic textures, exsolution lamellae in clinopyroxenes and orthopyroxenes, and low equilibration temperatures (630 to 800 oC). They have high Mg# in olivines (median: 92.1) and orthopyroxenes (median: 92.4) as well as variable Cr# in spinels (13 to 47; median: 37). Clinopyroxenes show variable LREEN enrichment (LaN/SmN=0.24 to 3.8) which is consistent with secondary re-enrichement processes. Trace element compositions of the garnets and clinopyroxenes in the garnet-bearing xenoliths indicate cryptic melt metasomatism as well as modal metasomatism associated with the introduction of phlogopite. Clinopyroxene-based geothermobarometry on clinopyroxene xenocrysts (25 out of the106) and one garnet lherzolite xenolith indicate a 39 to 40 mW/m2 model paleogeotherm, which overlaps at greater depths with two non-touching garnet-orthopyroxene inclusion pairs recovered from Karowe diamonds. These data imply that the lithospheric mantle beneath Karowe is 210 km thick with a diamond window of approximately 90 km thickness, which is consistent with other estimates of lithospheric depths in this region of the Zimbabwe Craton derived from petrology and geophysics. The major- and trace-element compositions of mineral inclusions in the diamonds indicate that 53 % are derived from eclogitic sources, 44 % are peridotitic, 2% have a sublithospheric origin, and 1 % are websteritic. The sublithospheric inclusion suite consists of three eclogitic garnets containing a majorite component (>6.12 to 6.46 apfu Si; with [O] = 24). This new observation of superdeep mineral inclusions in Karowe diamonds is unique within the Orapa cluster and may provide a key link to the presence of exceptionally large diamonds from this mine.From the present diamond suite, Karowe diamonds have variable morphologies with a dominance of octahedra (30 %), macles (20 %), and moderately resorbed morphologies (transitional between octahedra and dodecahedra; 18 %). The remaining 32 % are made up of 10 % rounded dodecahedra, 4 % cubo-octahedra, 2 % pseudo-hemimorphic and 16 % aggregated crystals. Overall, diamonds have FTIR nitrogen contents that range from below the limit of detection (?15 at.ppm) to 1217 at.ppm with variable nitrogen aggregation states (0 to 100 %B) and ?13C values from -34.5 to -2.0 ‰. Eclogitic diamonds contain 24 to 1217 at.ppm nitrogen with a median of 513 at.ppm and their carbon isotope compositions range between -21.5 and -2.5 ‰ with a median at -4.9 ‰. Peridotitic diamonds contain up to 937 at.ppm nitrogen with a median of 129 at.ppm. The majority of peridotitic diamonds fall into a typical mantle-like ?13C range (-8.6 to -2.0 ‰), with the exception of two diamonds that display unusual strongly 13C-depleted isotope compositions (-34.5 and -14.9 ‰). The mode in ?13C values for peridotitic diamonds (in class -4.0 to -3.5 ‰) is offset by about +1 ‰ relative to eclogitic diamonds (mode in class -5.0 to -4.5 ‰). These results could reflect derivation of mantle-like carbon from different sources through time for the two main parageneses or relate to the speciation of carbon fluids with constant ?13C (e.g., a minor increase in the CO2/CH4 ratio in the diamond-forming fluid from peridotitic to eclogitic diamonds).
International Journal of Mining and Geo-Engineering, Vol. 53, 2, pp. 1-11. pdf
India, Andhra Pradesh
deposit - Wajrakarur
Abstract: A plausible case of collective and economical mining of diamondiferous kimberlite deposits of Wajrakarur and adjoining places in Andhra Pradesh, southern India, along with the whole-rock geochemical evidences in support of their diamond potentiality are discussed in this article. The kimberlites/lamproites are mantle-derived ultrabasic rocks which rarely carry diamonds from mantle to the earth's surface through carrot-shaped intrusions referred to as pipes. Even though few hundreds of diamondiferous kimberlite pipes were discovered in India so far, there is no other production unit than Panna diamond mine in the country where primary rock is mined. In ancient India, diamond mining in south India in the Krishna river valley was well-known to the world fascinated by famous gemstones like Koh-i-Noor, Hope, Darya-e-Noor, Noor-ul-ain etc. which were mainly extracted from alluvium or colluvium in Krishna river valley. Having bestowed with more than 45 kimberlite pipes, the Wajrakarur kimberlite field (WKF) forms a favourable region for initiating diamond mining in the country. Geochemically, majority of the WKF show low TiO2 content and considerably high diamond grade (DG) values (>3) except some pipes viz., P-5 (Muligiripalli), P-13 (Tummatapalli) and P-16 (Pennahobilam) are barren due to high TiO2 and ilmenite contents. The TiO2 content (0.66-6.62 wt %) is inversely proportional to the DG (3.33 to 22.13). The DG value of some of the WKF pipes is close to that of Panna (8.36). The cationic weight% values clearly portray the diamondiferous nature of these deposits. The WKF pipes were also proved to be diamondiferous by exploratory drilling and bulk sample processing results by the government and multinational organisations. In southern India, due to several reasons, diamond mining has not seen its initiation and impetus till now although it records a considerable number of fertile kimberlite pipes at Wajrakarur, Lattavaram, Chigicherla, Timmasamudram etc. Though the majority of WKF diamondiferous kimberlite deposits in Wajrakarur are small in their areal extent (0.06-4.48 Ha) some of them are large (>10 Ha up to 120 ha). They occur in close proximity to each other offering feasibility for collective mining and winning the precious stone through a central processing unit by deploying the latest processing technologies. The geographic conditions of this region such as availability of human resources, water resources, vast open lands, wind power generation etc. also support to initiate mining of kimberlite pipes in this area. The availability of rough diamonds produced from local mines will make the polishing industry to meet its business needs during circumstances of the shortage of rough stone influx from foreign. Hence, although it demands liberal investments, reviving diamond mining in southern India can be materialised with a meticulous evaluation of these deposits ascertaining profitability. This will certainly help to restore the past glory of diamond mining in the southern part of the subcontinent.
Diamonds and Related Materials, in press available 36p. Pdf
Africa, Ghana
deposit - Akwatia
Abstract: Magnetic mineral inclusions, as iron oxides or sulfides, occur quite rarely in natural diamonds. Nonetheless, they represent a key tool not only to unveil the conditions of formation of host diamonds, but also to get hints about the paleointensity of the geomagnetic field present at times of the Earth's history otherwise not accessible. This possibility is related to their capability to carry a remanent magnetization dependent on their magnetic history. However, comprehensive experimental studies on magnetic inclusions in diamonds have been rarely reported so far. Here we exploit X-ray diffraction, Synchrotron-based X-ray Tomographic Microscopy and Alternating Field Magnetometry to determine the crystallographic, morphological and magnetic properties of ferrimagnetic Fe-oxides entrapped in diamonds coming from Akwatia (Ghana). We exploit the methodology to estimate the natural remanence of the inclusions, associated to the Earth's magnetic field they experienced, and to get insights on the relative time of formation between host and inclusion systems. Furthermore, from the hysteresis loops and First Order Reversal Curves we determine qualitatively the anisotropy, size and domain state configuration of the magnetic grains constituting the inclusions.
Abstract: Three main cycle of kimberlite magmatism are known for the Siberian Platform (SP) to date: Middle Paleozoic (D3), and two Mesozoic (T2-3 and J3). All economic highgrade kimberlites are of Middle Paleozoic (MP) age, and this feature is related with influence of melts/fluids of Permian-Triassic Siberian Super Plume produced huge changes in structure and composition of the SP Lithospheric Mantle (LM) including its enrichment by basaltic components, thinning, increase of fo2 and resorption of diamonds. Nevertheless, there are incredible differences in amounts of kimberlite bodies and their average diamond grade between different kimberlite fields of MP age, and these features are connected with intensity of carbonatite and silicate types of metasomatic treatment of the most deep-seated SP LM depleted peridotites especially of Lithosphere-Asthenosphere (LA) interaction zone. U-type lithospheric diamond formation is related with initial stage of carbonatite metasomatism, and its increase produce wehrlitezation and then carbonation of initial Cr-pyrope harzburgites and dunites but not related with diamond formation. Minor scale of silicate metasomatism of these modified LM peridotites produced conditions for generation of insignificant amount of kimberlite melts which form kimberlite fields with few bodies, but significant part of them are presented by high-grade kimberlite. And in case of significant scale of both carbonatite and silicate metasomatism of the LM peridotites produce large volume of kimberlite melt and hundreds of kimberlite bodies in fields with minor amonts of high grade ones.
Abstract: Petrogenesis of a newly discovered diamondiferous kimberlite pipe (3-021) by the Rio Tinto Group, ~2 km east of Dibbasanipalli, Wajrakarur Kimberlite Field, eastern Dharwar craton is attempted. The pipe is located in field based on published literature and consultation with local villagers [1,2]. Local geology is dominated by Archaean basement granitoids and genisses intruded by younger nordmarkites and dolerites. The rock is highly chloritised giving rise to poor preservation of kimberlitic matrix. However, olivine pseudomorphs are distinctly visible in thin sections. The rock possesses crustal xenoliths of granite, syenite, dolerite etc. with petrographic similarities to Khaderet pipe (3-106). Geochemically, the kimberlite is silica undersaturated (SiO2 39.32-45.67 wt%), MgO rich (26.51- 28.82 wt%) with K2O (1-88-2.1 wt%) higher than Na2O (0.29-0.39 wt%), akin to archetypal Group-I variety. High amounts of MgO and Mg# correspond to enrichment of magnesium bearing mineral phases like olivine and to some extent Mg-ilmenite. The higher concentration of elements Ba, Cr, Co, Nb, Ni, V, Zr is attributed to enrichment of mantle originated xenocrysts like chromite, perovskite, pyrope, Crdiopside. Based on trace element content, the kimberlite appears to be of magmatic origin within a stable continental geological set up. The enrichment of LREE over HREE supports inferior degree of partial melting (0.1-2%) indicating a metasomatically enriched phlogopite bearing garnet lherzolite source, inturn indicating a deep seated and depleted mantle origin, within an estimated temperature range of 1150- 1280oC and low viscosity (0.05 Pa s).
Abstract: The Mt. Vulture (Basilicata, Southern Italy) is an alkaline carbonatite volcano whose extrusive rocks are mafic, alkaline with different Na/K ratios, mainly SiO2 undersaturated, with relatively high contents of Cl, S, F, and CO2 [1]. Their composition ranges from basalts to basanites to tephrite to phono-tephrites and phonolites. Along with this magma suite have been erupted mantle xenolith bearing-carbonatitic melilitites and carbonatites [1, 2]. Holocrystalline ejecta have been studied in detail to reconstruct the composition of the subvolcanic/plutonic bodies beneath Mt. Vulture. The ejacta are haüine-bearing clinopyoxenites with variable content of olivine, amphibole and phlogopite, haüine foidolites with some nepheline and leucite, haüine-calcite-syenites, syenites, calcite melilitolites, K-feldspar bering-alvikites and a sovite [3]. There is a continuous variation in the modal and geochemical composition between clinopyroxenite and foidolite, that might be related to the chemical evolution shown by the extrusive rocks. The ejecta show an enrichment trend in LILE, LREE and HFSE consistent with fractional crystallisation evolution, from clinopyroxenites to foidolites and from foid-syenites to syenites. The foid-syeniites are rich in U, Pb, Sr, LREE and contain britholite, wholerite, Upyrochlore. The most evolved syenite however, is less enriched in REE but contains elevate content of U and HFSE. The sovite contains intercumulus alkali carbonates. A glimemerite vein in a haüine foidolite contain REE-rich apatite, shorlomite and U-pyrochlore. These findings suggest that alkaline-alogen-H2O-CO2 rich fluids can be formed during sub-volcanic/plutonic fractional crystallisation. These fluids can produce fenitisation and/or can form mineralisation enriched in REE and HFSE. The ejecta suite studied represents the intrusive complex beneath the volcano and these rock types are typical of ring complexes in alkaline carbonatite volcanoes.
Mineralogy and Petrology, in press available 20p. Pdf
Russia, Archangel
deposit - Grib
Abstract: In this paper, new main and trace elements and isotopic data are presented for 14 coarse-grained eclogite xenoliths from the V. Grib kimberlite pipe in the central part of the Arkhangelsk Diamondiferous Province. Based on reconstructed whole rock MgO content, this suite is divided into high-MgO and low-MgO varieties. Eclogitic groups have a similar range of variations in the trace element compositions of garnet, clinopyroxene and reconstructed whole rock. All eclogites show positive Eu anomalies in garnet and Sr anomalies in the whole rock. The negative correlation between the Mg#, Sr/Lu ratio and HREE in a whole rock points to upper and lower oceanic crustal rocks as a protolith for eclogites with high and low whole rock HREEs, respectively. Low-MgO eclogites with higher whole rock HREEs have the basaltic upper oceanic crustal protolith, whereas the protoliths of eclogites with lower whole rock HREEs could be of gabbroic composition from the lower oceanic crust. High-MgO eclogites could represent MgO-rich portions of oceanic crustal rocks: picritic/MgO basalt portions in the upper oceanic crust and troctolite portions in the lower oceanic crust. The Sr and Nd isotope compositions suggest a complex history of eclogites during their residence in the lithospheric mantle. Similarities in the Nd isotope compositions and two-point Sm-Nd isochron ages are evidence for re-equilibration of the Sm-Nd isotope system between the eclogite garnet and clinopyroxene via a pre-kimberlite thermal event at 396?±?24 Ma. The subset of clinopyroxenes from four eclogites has a Sr isotope composition that plots on the isochron at an age of 2.84 Ga, which reflects the time of the subduction event and emplacement into the lithosphere and corresponds to the time of the Belomorian Eclogite Province of Baltic Shield formation.
Abstract: The late evolution of kimberlite magmas, i.e., during and-following emplacement into the upper crust, remains a-controversial aspect of kimberlite petrogenesis. Likewise, it is-unclear whether or not there is a link between melt composition-and the emplacement mechanism of intrusive kimberlites (i.e.,-planar dykes/sills vs. irregular intrusions in the root zone of-pipes). Resolving these issues is hampered by the absence of-comparative studies of late-magmatic kimberlite phases (e.g.,-apatite, monticellite, mica) in dykes, sills, and root-zone-intrusions from the same locality.-Here we report petrographic and mineral-chemical results-for groundmass phases in samples of dykes, sills, and root zone-intrusions from the Kimberley kimberlites (South Africa).-Early crystalised phases (e.g., olivine, spinel) in dykes/sills and-root-zone intrusions have indistingushable compositions, and-hence crystallised from similar primitive melts. Conversely,-apatite major element compositions are variable and can-discriminate dykes/sills (i.e., low and constant Sr, with-increasing Si) from root zone intrusions (high but variable Sr,-low and constant Si). The Sr depletion in root zone apatite is-interpreted to represent fractional crystallisation of earlier-apatite, perovskite, and calcite from a broadly similar parental-melt. Silica enrichment of apatite from dykes/sills may be-attributed to the coupled incorporation of CO32- and Si into the-apatite structure, reflecting higher CO2 contents in the melts-that formed dykes/sills. CO2 enrichment in the dykes/sills is-consistent with petrographic obervations. Dykes/sills are-enriched in carbonates, may contain dolomite, and are depleted-in mica and monticellite compared to the groundmass of rootzone-kimberlites. This suggests the melts parental to-dykes/sills have a higher CO2/H2O ratio compared to those-parental to root zone intrusions. These two distinct melt-evolution paths cannot be due to crustal contamination before-emplacement because the Sr-isotope compositions of latecrystallised-carbonates are indistinguishable in dykes/sills and-root-zone intrusions. We speculate that CO2 is better retained-in dykes/sills due to a higher confining pressure (i.e., lack of-breakthrough to the surface).-
Abstract: Kyanite-eclogite xenoliths from Wajrakarur are considered as remnants of subducted ocean-floor crust [1]. Here trace element concentration and isotopic data are presented in garnet (Grt) and kyanite (Ky) from xenoliths KL-2 E1-E4, characterized by [2]). We use the precise 87Sr/86Sr host kimberlite groundmass perovskite ratio (0.70312-0.70333, [3]) as a proxy for the extent of kimberlitic magma infiltration at 1.1 Ga. The xenolithic Grt and Cr-rich (upto 1506 ppm) Ky have more radiogenic 87Sr/86Sr values than kimberlite, at 1.1 Ga, of 0.703829-0.705203 and 0.703811-0.704502, respectively. Furthermore, the Grt and Ky 143Nd/144Nd ratios, at 1.1 Ga, are 0.509321-0.511372 and 0.510951-0.511156, respectively, and are distinctly lower than those of the host kimberlite (0.511870-0.512290, [4]). This indicates that the infiltration of kimberlitic fluid has not altered the 87Sr/86Sr and 143Nd/144Nd ratios in the Grt and Ky, and therefore their isotope compositions must be inherited and predate the kimberlite magma generation event at 1.1 Ga. Trace elements in Grt and Ky indicate extreme metasomatism (Sr in Grt 104-296 ppm, in Ky 672-8713 ppm [limit Sr<2ppm] and Nb in Grt 0.64-1.78 ppm, in Ky 1.7-4.54 ppm [limit Nb<0.5ppm]). The xenoliths underwent at least one major melting event inferred from extreme depletions in Re, Os and 177Os/178Os ratios [5]. Their mantle-like ?18O values (Grt 5.3-5.4‰, Ky 5.3-5.9‰), positive Eu anomalies in both Grt and Ky (similar to Group 1 HREE-depleted garnets of [1]) suggests that the protolith likely was a chromite-bearing leucogabbro, emplaced as a high-pressure cumulate at the crust-mantle boundary, which was later eclogitized due to deep-seated subduction and underwent episodes of extreme melting and metasomatism before 1.1 Ga and at least before 1.7 Ga, as inferred from their youngest Re depletion dates [5].
Abstract: Studies on fluid inclusions in carbonatitic rocks are essential to understand the physicochemical processes involved in carbonatite-related hydrothermal ore mineralization. Although little is known about the composition of carbonatite-derived fluids. We investigated fluid inclusions in the Kaiserstuhl carbonatites, SW Germany [1,2] and identified four different types typically known from carbonatitic systems worldwide [3]: (I): Vapor-poor H2O-NaCl fluids with <50 wt.% salinity. (II): Vapor-rich H2O-NaCl-CO2 fluids with <5 wt.% salinity. (III): Multi-component fluids with high salinity and CO2. (IV): Multi-component fluids with high salinity, no CO2. Homogenization temperatures (156 to 530°C) of all fluid types generally show a wide range [this study, 2]. Primary type I fluid inclusions occur in early magmatic olivine/monticellite, as well as paragenetically later apatites and calcites [2]. This indicates a ubiquitous existence of a saline brine, which does not reach saturation with respect to halite, during early to late crystallization stages. Liquidus surface modelling based quantifications for fluid type III suggest that carbonatite melts predomonantly exsolve Na-K-sulfate-carbonate/bicarbonate-chloride brines (type III or IV, respectively). Such fluid inclusions, with type III (CO2-free) on one side and type IV (and II, both CO2-rich) on the other side, may represent immiscible fluids that were trapped after segregation by boiling from a parental highly saline brine (type I). Fluid boiling, in turn, is probably triggered by a rapid pressure release during “pneumatic hammer-like,” discontinuous melt ascent.
Abstract: Mountain Pass is one of the largest and most economically important REE deposits in the world. The ore body is a carbonatite stock within a shonkinite and syenite plutonic complex, which is part of a ~130 km long trend of Mesoproterozoic alkaline igneous rocks in the southeast Mojave Desert [1]. Zircons from a suite of shonkinite and syenite rocks at Mountain Pass were analyzed by SHRIMP-RG (207Pb/206Pb ages and trace elements) and SIMS (O isotopes) to elucidate their petrogenesis and potential relationship to ore-forming carbonatite. Concordant 207Pb/206Pb dates define multimodal distributions from ~1370-1435 Ma and ~1530-1780 Ma. The youngest 207Pb/206Pb dates of ~1370-1380 Ma and ~1390-1400 Ma overlap published Th-Pb monazite ages of 1371 ± 10 Ma and 1396 ± 16 Ma for the carbonatite ore body and a smaller carbonatite dike at Mountain Pass [2]. The youngest (<1435 Ma) zircons, interpreted to be magmatic (autocrystic), have REE up to ~10,000x chondrite values, subtle (~0.8) Eu/Eu* anomalies, generally low U (<500 ppm), moderate Hf (<11,000 ppm), and Ti-in-zircon temperatures that cluster at ~800 °C. Paleoproterozoic zircon xenocrysts have larger Eu/Eu* anomalies (~0.1- 0.5) and extend to higher Hf contents (>11,000 ppm). Zircon ?18O values in the <1435 Ma grains span from mantle (~5‰) to supracrustal (~7‰), and are mostly in the higher supracrustal end of the range. Paleoproterozoic zircons overlap this range as well as extend to higher ?18O values (~9‰). Our new data support coeval and longlived (20 Myr+) alkaline and carbonatite magmatism and underscore the relative importance of the crust in generating magmas associated with the world-class Mountain Pass REE deposit.
Abstract: This paper presents the first major and trace element compositions of mantle-derived garnet xenocrysts from the diamondiferous No. 30 kimberlite pipe in the Wafangdian region, and these are used to constrain the nature and evolution of mantle metasomatism beneath the North China Craton (NCC). The major element data were acquired using an electron probe micro-analyzer and the trace element data were obtained using laser ablation inductively coupled plasma-mass spectrometry. Based on Ni-in-garnet thermometry, equilibrium temperatures of 1107-1365 °C were estimated for peridotitic garnets xenocrysts from the No. 30 kimberlite, with an average temperature of 1258 °C, and pressures calculated to be between 5.0 and 7.4 GPa. In a CaO versus Cr2O3 diagram, 52% of the garnets fall in the lherzolite field and 28% in the harzburgite field; a few of the garnets are eclogitic. Based on rare earth element patterns, the lherzolitic garnets are further divided into three groups. The compositional variations in garnet xenocrysts reflect two stages of metasomatism: early carbonatite melt/fluid metasomatism and late kimberlite metasomatism. The carbonatite melt/fluids are effective at introducing Sr and the light rare earth elements, but ineffective at transporting much Zr, Ti, Y, or heavy rare earth elements. The kimberlite metasomatic agent is highly effective at element transport, introducing, e.g., Ti, Zr, Y, and the rare earth elements. Combined with compositional data for garnet inclusions in diamonds and megacrysts from the Mengyin and Wafangdian kimberlites, we suggest that these signatures reflect a two-stage evolution of the sub-continental lithospheric mantle (SCLM) beneath the NCC: (1) early-stage carbonatite melt/fluid metasomatism resulting in metasomatic modification of the SCLM and likely associated with diamond crystallization; (2) late-stage kimberlite metasomatism related to the eruption of the 465 Ma kimberlite.
Abstract: A new Massadou kimberlite field, was discovered in southeastern Guinea, near the town of Macenta. It consists of 16 poorly diamondiferous kimberlite dikes, ~1 m thick on average. The ore-controlling zone has a width of around 600 m, its orientation corresponds to the K-4 trend after S. Haggerty, and it is quite well detectable in satellite images. A thick laterite weathering profile has developed on the kimberlites. The main indicator minerals are pyrope, chromite, and ilmenite. Ilmenite grains have a zoned structure with a high-Fe core (hemoilmenite) overgrown by a parallel-columnar aggregate of Mg-ilmente rim resulting from interaction of the core phase with kimberlitic melt. The age of kimberlites is estimated as 140-145 Ma by analogy with those in adjacent areas. Dikes occur as an independent form of kimberlite magmatism in the Guinean-Liberian shield, rather than being roots of kimberlite pipes; therefore, the erosion cutout is relatively small and large-scale diamond placers should not be expected.
Abstract: Kimberlites are silica-poor, volatile-rich (CO2 ± H2O), volcanic rocks that are often described as ‘hybrid’, because their parental magmas include abundant xenocrystic (crustand mantle-derived) components. Unravelling the influence of mantle assimilation on kimberlite melt compositions represents an outstanding question of kimberlite petrology. To address this issue, we have carried out a comprehensive geochemical and petrographic investigation of nine kimberlites from the Kaavi-Kuopio field in Finland, that were emplaced on the southern margin of the Karelian Craton in the Neoproterozoic (~550-600 Ma). Olivine is the dominant mineral phase in kimberlites (~50 vol.%) with cores mainly derived from the disaggregation of mantle peridotite. In contrast, olivine rims crystallise directly from the kimberlitic melt and their Mg# (Mg/(Mg+Fe)) typically show remarkable homogeneity within and between kimberlites of a single cluster and field (e.g., Lac de Gras). The Kaavi-Kuopio kimberlites appear to represent a unique case where there is a (statistically) significant difference between the average Mg# of olivine rims in different pipes (89.9 ± 0.2 to 88.5 ± 0.3). Importantly, the Mg# of olivine rims exhibit a strong correlation with the Mg# of olivine cores. Furthermore, the compositions of olivine cores (and rims) exhibit a strong correlation with those of spinel (e.g., Mg#, TiO2 contents). These geochemical variations correlate with the modal mineralogy of the kimberlites: for example, higher abundances of monticellite and lower abundances of ilmenite are associated with higher Mg# olivine. The robust relationship between entrained and assimilated lithospheric mantle material (i.e. olivine cores) and magmatic components (i.e. olivine rims, spinel, and other groundmass minerals) suggests that assimilation of lithospheric mantle has impacted the compositions of kimberlitic melts to a greater extent than previously recognised. These new data also suggest significant variations in the composition of the mantle lithosphere beneath the Kaavi-Kuopio kimberlites, which are spaced less than 10 km apart.
Abstract: Mantle xenoliths brought up by kimberlitic magmas are the main source of data on the composition and physical conditions of cratonic mantle. Temperature varioations in a complete lithospheric mantle section (80-200 km) of the Siberian craton beneath the Upper Muna kimberlite filed are estimated based 49 peridotite xenolith and 330 Cpx grains from the Komsomolskaya-Magnitnaya pipe. Pressure and temperature estimates closely follow the 34.5 mW/m2 conductive geotherm. Thermal lithospere thickness is of ~ 220 km, and “diamond window” in the Paleozoic is ~75 km thick (Fig.1). Olivine compositions range in Mg# from 82 to 94 and the majority of olivenes has very high Mg# > 93. Garnets compositions mainlly follow to harzburgite-dunite and lherzolite trends plotted as Cr2O3 vs CaO. The composition of the minerals indicated the extremly depleted lithospheric mantle beneath the Upper-Muna kimberlite field. Figure 1: Model palaeogeotherms calculated using the program FITPLOT. Komsomolskaya-Magnitnaya - our data, Novinka and Udachaya are from Z16 [1]
Microscopy and Microanalysis ( M&M)Co. Conference, Sept. 9, posters 1 p. each
Europe, Israel
deposit - Kishon
Abstract: The Microscopy and Microanalysis (M&M) conference in Portland Oregon, USA is one of the biggest microscopy conferences in the world and this year it hosted its largest meeting in history with over 3,300 participants, up to 20 parallel sessions and over 600 posters. The two posters were presented by Sarah E.M. Gain who is from the University of Western Australia where she trains and supports researchers in Microscopy, Characterisation and Microanalysis. Sarah discussed some of the unique gem material collected from Shefa Gems’ exploration activity in the Kishon Mid Reach and Rakefet Magmatic Complex, analysed using a range of microscopy and microanalysis techniques. She also discussed the scientific importance of this material.The first poster looked at hibonite (a Ca-Al-oxide) with inclusions of vanadium metal. The second poster looked at, Cr corundum (ruby), which is unusual due to the extremely high Cr levels and the inclusions of Cr metal.
Journal of Raman Spectroscopy, in press available, 19p. Pdf
Russia
deposit - Udachnaya
Abstract: The study of kimberlite rocks is important as they provide critical information regarding the composition and dynamics of the continental mantle and are the principal source of diamonds. Despite many decades of research, the original compositions of kimberlite melts, which are thought to be derived from depths > 150 km, remain highly debatable due to processes that can significantly modify their composition during ascent and emplacement. Snapshots of the kimberlite?related melts were entrapped as secondary melt inclusions hosted in olivine from sheared peridotite xenoliths from the Udachnaya?East pipe (Siberian craton). These xenoliths originated from 180? to 220?km depth and are among the deepest derived samples of mantle rocks exposed at the surface. The crystallised melt inclusions contain diverse daughter mineral assemblages (>30 mineral species), which are dominated by alkali?rich carbonates, sulfates, and chlorides. The presence of aragonite as a daughter mineral suggests a high?pressure origin for these inclusions. Raman?mapping studies of unexposed inclusions show that they are dominated by carbonates (>65 vol.%), whereas silicates are subordinate (<13 vol.%). This indicates that the parental melt for the inclusions was carbonatitic. The key chemical features of this melt are very high contents of alkalis, carbon dioxide, chlorine, and sulfur and extremely low silica and water. Alkali?carbonate melts entrapped in xenolith minerals likely represent snapshots of the primitive kimberlite melt. This composition is in contrast with the generally accepted notion that kimberlites originated as ultramafic silicate water?rich melts. Experimental studies revealed that alkali?carbonate melts are a very suitable diamond?forming media. Therefore, our findings support the idea that some diamonds and kimberlite magmatism may be genetically related.
Abstract: Kimberlite field is an example of widespread Mesoproterozoic intracontinental magmatism. Recent studies have identified deep subcontinental lithospheric mantle as a source region of the kimberlite magmatism while timing, origin, and processes responsible for the generation of coeval lamprophyres remain poorly constrained. Here, we present and discuss new petrological and geochemical data for two lamprophyre dykes from the Wajrakarur kimberlite field and assess their petrogenetic relation to the kimberlite occurrences. Based on mineral compositional and whole?rock geochemical characters, it is suggested that lamprophyres are formed through low degrees of partial melting of “enriched” lithospheric mantle that was modified and metasomatized by melts derived from recycled crust. This differs from geochemical imprints found in coeval kimberlites, where a crustal source component appears to be absent and is more consistent with rock derivation from “depleted” lithosphere which has experienced interaction with asthenosphere?derived melts. An apparent lack of garnet in the mantle sources of lamprophyres is suggestive of melting at comparatively shallow depth (~100 km) relative to the kimberlites. Hence, these geochemically contrasting rocks, although have formed at the same time, are derived from vertically heterogeneous lithospheric mantle sources and can be explained through and linked with a thermal anomaly in the underlying convective asthenosphere. We suggest that the deeper mantle source region of the kimberlites was more pristine and devoid of subduction?related signatures, whereas the shallower mantle source region of the lamprophyres seems to have preserved imprints of plate convergence and subduction associated with the evolution of the Dharwar Craton.
The Journal of the Southern African Institute of Mining and Metallurgy, Vol. 119, pp. 97-103.
Africa, South Africa
deposit - Finsch
Abstract: Accurate delineation of the contact between a kimberlite pipe and country rock at production level depths is a challenge due to limited geological data. Geological information is obtained from widely spaced diamond core boreholes which are drilled either from surface or from higher mining levels within the pipe. Kimberlite pipe/country rock contacts are notoriously irregular and variable, further reducing the confidence in contact positions defined by the drill-holes. At Finsch Diamond Mine (FDM), the opportunity arose to further improve the confidence in the contact positions relative to the planned slot (end) positions of each sublevel cave tunnel during the development stage of these tunnels. As a result, the accuracy of the 3D geological model has improved.
The use of diamond drill core for this purpose is expensive due to site establishment requirements. The lengthy time taken during site establishment also delays the development of tunnels and support cycles, thereby extending the completion dates. FDM has reduced delays during development by adopting percussion drilling, in conjunction with gamma ray logging. The S36 drill rig is mounted on a moveable platform and does not require a costly and lengthy site establishment. The holes are generally drilled (0°/flat) on grade elevation, and these holes could also be drilled from the rim tunnels (developed in waste) into the kimberlite pipe. A single-boom production drill rig is normally used to drill holes about 20 m in length. On completion of the contact delineation drilling, gamma logging of the holes is conducted using the GeoVista geophysical sonde (or probe) to log the natural gamma signature of the dolomite/ kimberlite contact. The advantage of this tool is that the readings are continuous within centimetre intervals, and due to contrasting characteristics between kimberlite (rich in clay minerals) and dolomite, the contact position can be determined accurately. The better definition of contact positions also adds value to tunnel stopping distance in terms of developing the tunnel's slot at the optimum distance from the contact (easier blasting of longhole rings, avoidance of contact overbreak and premature waste ingress, and other matters relating to extraction of ore from these tunnels). This method is highly successful and has reduced development costs (on-time completion), improved definition of the pipe's contact position for geological modelling, improved blast design, and mitigated early waste ingress by maintaining the contact's integrity.
Abstract: Detailed studies have shown that a change in the eudialyte occurrence forms (and the moment of its crystallization) is a new geochemical criterion for rare metal ore content in alkalic magmas (eudialyte ores). A new principle of the presence of ores in alkalic magmas has been formulated: a prerequisite for the formation of an ore deposit is early saturation of alkalic magmas with an ore mineral. If the ore component concentration is significantly lower than the cotectic (saturation), then melt saturation and crystallization of an ore mineral will take place at later stages of rock formation in a small volume of the interstitial melt, when the phenomena of convective?gravity differentiation and segregation of mineral phases in the form of ore deposits are hampered. This leads to dispersion of the ore components in the form of xenomorphic grains of accessory minerals. Rocks of the differentiated complex (lower zone of the Lovozero deposit) and rocks of the Khibiny massif contain xenomorphic eudialyte and are not promising for eudialyte ores. Eudialyte deposits are associated with the upper zone of the Lovozero intrusion where euhedral early eudialyte occurs. The initial magma is saturated with eudialyte after crystallization of about 80% of the intrusion. The proposed criterion is applicable to the largest alkalic massifs in the world. The Ilimaussaq massif (Greenland), the rocks of which contain early crystallized, euhedral eudialyte, hosts a superlarge eudialyte ore deposit. Unlike the Khibiny massif and the Pilanesberg alkalic complex, the rocks of which contain late xenomorphic eudialyte, this massif has no deposits of this type.
Geochemistry International, Vol. 57, 9, pp. 963-980.
Russia
deposit - Lomonosov
Abstract: The data on the composition of microinclusions in diamonds from the Lomonosov deposits are reported for the first time. The studied diamonds include “coated” (n = 5) and cubic (n = 5) crystals. The estimated range of the degree of nitrogen aggregation in diamonds (4-39% B1) does not support their direct links with kimberlite magmatism; however, their short occurrence in the mantle at higher temperatures is probable as well. The composition of melt/fluid microinclusions in these samples varies from essentially carbonatitic to significantly silicate. It is shown that the contents of MgO, CaO, Na2O, Cl, and P2O5 decrease with increasing content of silicates and water. Different mechanisms of the generation and evolution of diamond-forming media are discussed to explain the observed variations.
Abstract: The recent discovery of alluvial diamonds in Marange, Zimbabwe, has rekindled the interest of environmental scholars in critiquing the political economy of artisanal mining. The increasing recurrence of this 'illegal' small-scale mining has partly been attributed to its 'lucrative' nature, but more importantly as a safety net to the deepening crises rooted in the country's adverse economic climate in the period under review. The economic structural adjustments during the 1990s, the hefty off-budget gratuities awarded to restive war veterans in 1997, the country's ill-fated intervention in the DRC war in 1988 and the violent land seizures of the early 2000s have contributed to this prolonged setback. This paper first assesses the sustainability of artisanal mining as a livelihood option mostly for the unemployed. It appears that diamond mining produced positive outcomes for some, but by no means all, artisanal miners who accumulated considerable wealth in cattle and real estate. Others failed to break through altogether, suffering heavy losses, including deaths under mining pits. The paper then explores the effects of artisanal mining on the physical environment, including river denudation and soil erosion, deforestation, creation of wastelands and pollution of water bodies. The overriding argument of this study is that artisanal mining has continued to be a sustainable livelihood avenue in spite of its well-known negative impacts. The study is based on semi-structured interviews conducted between 2015 and 2017 with artisanal miners, security personnel, rural district councillors, environmental authorities and former employees of defunct mining firms in Marange. Other sources of data included community-based organisations and civil society groups, as well as newspapers that reported on the unfolding events in Marange at the time.
Abstract: Goldschmidtite is a new perovskite-group mineral (IMA No. 2018-034) with the ideal formula (K,REE,Sr)(Nb,Cr)O3. A single grain of goldschmidtite with a maximum dimension of ?100 ?m was found as an inclusion in a diamond from the Koffiefontein pipe in South Africa. In addition to the dark green and opaque goldschmidtite, the diamond contained a Cr-rich augite (websteritic paragenesis) and an intergrowth of chromite, Mg-silicate, and unidentified K-Sr-REE-Nb-oxide. Geothermobarometry of the augite indicates that the depth of formation was ?170 km. The chemical composition of gold-schmidtite determined by electron microprobe analysis (n = 11, WDS, wt%) is: Nb2O5 44.82, TiO2 0.44, ThO2 0.10, Al2O3 0.35, Cr2O3 7.07, La2O3 11.85, Ce2O3 6.18, Fe2O3 1.96, MgO 0.70, CaO 0.04, SrO 6.67, BaO 6.82, K2O 11.53, total 98.53. The empirical formula (expressed to two decimal places) is (K0.50La0.15Sr0.13Ba0.09Ce0.08)?0.95(Nb0.70Cr0.19Fe0.05Al0.01Mg0.04Ti0.01)?1.00O3. Goldschmidtite is cubic, space group Pm3m, with unit-cell parameters: a = 3.9876(1) Å, V = 63.404(6) Å3, Z = 1, resulting in a calculated density of 5.32(3) g/cm3. Goldschmidtite is the K-analog of isolueshite, (Na,La)NbO3. Raman spectra of goldschmidtite exhibit many second-order broad bands at 100 to 700 cm-1 as well as a pronounced peak at 815 cm-1, which is possibly a result of local ordering of Nb and Cr at the B site. The name goldschmidtite is in honor of the eminent geochemist Victor Moritz Goldschmidt (1888-1947), who formalized perovskite crystal chemistry and identified KNbO3 as a perovskite-structured compound.
Abstract: A find of coesite in a kyanite graphite-diamond-bearing eclogite xenolith from the Udachnaya-Vostochnaya kimberlite pipe is described in this paper. The coesite relics were found in intensely fractured garnet indicating some influence of the kimberlite melt, which is supported by the typical secondary mineral assemblage around this inclusion. These data indicate that shallower diamond-free coesite-grade rocks (2.7 GPa) underwent metamorphism distinct from diamond-bearing coesite eclogites (?4 GPa). The metasomatic alteration of rock as a result of the C-O-H fluid-rock interaction during diamond crystallization may be another possible reason for the absence of coesite in diamond-bearing xenoliths.
Abstract: Diamonds and their inclusions are unique fragments of deep Earth, which provide rare samples from inaccessible portions of our planet. Inclusion-free diamonds cannot provide information on depth of formation, which could be crucial to understand how the carbon cycle operated in the past. Inclusions in diamonds, which remain uncorrupted over geological times, may instead provide direct records of deep Earth’s evolution. Here, we applied elastic geothermobarometry to a diamond-magnesiochromite (mchr) host-inclusion pair from the Udachnaya kimberlite (Siberia, Russia), one of the most important sources of natural diamonds. By combining X-ray diffraction and Fourier-transform infrared spectroscopy data with a new elastic model, we obtained entrapment conditions, Ptrap?=?6.5(2) GPa and Ttrap?=?1125(32)-1140(33) °C, for the mchr inclusion. These conditions fall on a ca. 35?mW/m2 geotherm and are colder than the great majority of mantle xenoliths from similar depth in the same kimberlite. Our results indicate that cold cratonic conditions persisted for billions of years to at least 200?km in the local lithosphere. The composition of the mchr also indicates that at this depth the lithosphere was, at least locally, ultra-depleted at the time of diamond formation, as opposed to the melt-metasomatized, enriched composition of most xenoliths.
The Journal of the Southern African Institute of Mining and Metallurgy, Vol. 199, pp. 613-620.
Africa, Lesotho
deposit - Liqhobong
Abstract: Liqhobong Mining Development Company (LMDC) has been experiencing problems with boulders after blasting where the fragment sizes exceed the maximum of 800 mm as per mine standard. As a result, the mine has employed various methods to improve the fragmentation. The goal is to produce a run-of-mine (ROM) feed that does not choke the crusher and cause delays in production. In order to achieve this goal, fragmentation distribution within the fines and coarse envelope must be optimized through effective planning of blasting activities and accurate execution. The mine determined the fines-coarse envelope within which the entire crushing system can handle fragments using Split Desktop software. It is expected that both the predicted and actual fragmentation curves lie within that envelope for optimal fragmentation. The Kuz-Ram model with blast design parameters of 2.6 m for burden, 2.8 m for spacing, and 127 mm hole diameter was used to predict the fragmentation. The results show that the blast design parameters may need altering to achieve optimum fragmentation. Furthermore, the execution of the drilling and blasting may be the cause of the fragmentation problems. The mean fragmentation size (X50) differs greatly, unlike the uniformity index (n)s values which are relatively close to each other (0.6 to 2.2). The mean squared error (MSE) values have a large range. A proposed solution is a modified burden, spacing, and hole diameter. It is concluded that blast design parameters need to be reviewed in order to obtain correct predictions.
Abstract: Magnetic mineral inclusions, as iron oxides or sulfides, occur quite rarely in natural diamonds. Nonetheless, they represent a key tool not only to unveil the conditions of formation of host diamonds, but also to get hints about the paleointensity of the geomagnetic field present at times of the Earth's history otherwise not accessible. This possibility is related to their capability to carry a remanent magnetization dependent on their magnetic history. However, comprehensive experimental studies on magnetic inclusions in diamonds have been rarely reported so far. Here we exploit X-ray diffraction, Synchrotron-based X-ray Tomographic Microscopy and Alternating Field Magnetometry to determine the crystallographic, morphological and magnetic properties of ferrimagnetic Fe-oxides entrapped in diamonds coming from Akwatia (Ghana). We exploit the methodology to estimate the natural remanence of the inclusions, associated to the Earth's magnetic field they experienced, and to get insights on the relative time of formation between host and inclusion systems. Furthermore, from the hysteresis loops and First Order Reversal Curves we determine qualitatively the anisotropy, size and domain state configuration of the magnetic grains constituting the inclusions.
Abstract: The spatial and temporal association between lamprophyres and kimberlites provides unique opportunities to explore their genetic relationships. This paper explores such a relationship by detailing mineralogical and geochemical aspects of Korakkodu lamprophyre dykes located within the well?known Mesoproterozoic diamondiferous Wajrakarur Kimberlite field (WKF), towards the south?western margin of Paleo-Mesoproterozoic Cuddapah Basin, Eastern Dharwar Craton, southern India. Mineralogy reveals that these dykes belong to calc?alkaline variety of lamprophyres, but their geochemistry display mixed signals of both alkaline and calc?alkaline lamprophyres. These lamprophyres are highly potassic, and their high Al2O3 and low?TiO2 content implies a shoshonitic character. Low Mg#, Ni, and Cr concentration highlight their evolved nature. High (La/Yb)N and (Gd/Yb)N content is consistent with their derivation from low degrees of partial melting, whereas highly fractionated nature suggests the presence of garnet in their source. Absence of prominent Nb?Ta anomaly implies to the dilution of lithospheric mantle source by melts rich in HFSEs and low La/Nb ratio compared to those of the calc?alkaline island arc volcanics and suggests an asthenospheric overprint on lithospheric mantle source. Carbonatite metasomatism in the source region of these lamprophyres is apparent from conspicuously high?Zr/Hf ratio, and the HFSE budget of these lamprophyres are principally controlled by the presence of phlogopite veins in their lithospheric source. An extremely heterogeneous and layered lithospheric mantle beneath Eastern Dharwar Craton has been inferred from the divergent genetic history of Mesoproterozoic lamprophyres and kimberlites in the Wajrakarur field.
Abstract: Super Deep Diamonds (SDD) are known to form at depths between ~300 and ~1000 km in the Earth’s mantle [1]. These diamonds as well as their minerals, melts and fluid inclusions are rare natural materials from deep Earth. The aim of this study is to indentify and characterize mineral inclusions in diamonds from Juína, Mato Grosso, Brazil, and hence classify them as SDD (or not). Twelve diamonds from four different mining sites of Juína were selected according to their inclusions using an Estereo Microscope. The main diamond features were based on crystallographic faces, shape, degrees of resportion, crystal state and intergrowing [2]. Diamond samples are transparent, colorless and present octahedro, octahedro-tetrahexahedral and tetrahexahedral habits. Some diamonds show trigons with positive and negative relief, and hexagons with negative relief. Four diamonds are heavily resorbed and were classified as "unknowing habits", as their shapes are distorced and fragmented. Moreover, three samples show abrasion on the vertices of the quartenary axes, and the others have distinct degrees of resorption. Some crystals present intergorwth, such as contact twins (macle) in {111} or aggregates. All diamonds have mineral inclusions of different colors. Most inclusions are black and could be carbon spots, oxides or even silicates, such as olivine. Other inclusions are yellow to red, which might indicate garnet. In addition, blue inclusions were observed, and could be sulphides. The next steps consists of Fourier Transform Infrared (FTIR) to determine diamond nitrogen impurities, and Micro-Raman spectroscopy and X-Ray Diffraction analyses using Synchrotron radiation to determine in situ the chemical composition of mineral inclusions.
Abstract: Kimberlites are mantle-derived, CO2 and H2O rich magmas that entrain abundant mantle material, including diamonds during rapid ascent to the surface. Most kimberlite magmas that reach the upper crust either erupt explosively or are emplaced as shallow hypabyssal intrusions. Catastrophic volatile exsolution, local geology and stress regimes, and interaction with external water are suggested as possible controls of magma explosivity. A full understanding of the processes promoting the explosive emplacement of kimberlite magmas has been hindered by common alteration and crustal contamination of pyroclastic kimberlites (PK). To address this issue, we have undertaken a detailed petrographic and mineral-chemical study of fresh pyroclastic and hypabyssal kimberlites (i.e. dykes either cross-cutting or isolated from volcanic pipes) from the Diavik Diamond Mine (Lac de Gras, Canada). Diavik kimberlites feature the same olivine compositions regardless of emplacement style. The cross-cutting kimberlite dykes (xHK) and pyroclastic kimberlites also feature the same chromite (i.e. liquidus spinel) compositions, and spinel evolution to indistinguishable magnesian ulvospinel-magnetite compositions. These results demonstrate that primitive melt compositions, and early magmatic evolutionary trends are the same for kimberlite melts that erupt explosively or those that are emplaced as shallow intrusions. The magmaclasts in PKs contain higher abundances of phlogopite, and lower contents of carbonate than the groundmass of xHKs suggesting higher H2O/CO2 ratios in the magmas that erupt explosively. This finding highlights divergence of the PK and xHK parental melt compositions after late spinel formation, which underpins explosive CO2 exsolution only in some magmas. While the causes of explosive volcanism remain uncertain, our study indicates that primitive melt composition has no significant influence on the emplacement style of kimberlites.
Abstract: Mantle xenolith from Komsomolskya and Zarnitsa pie were used for the reconstryctions of mantle columns beneath theses kimberlite pipes. Relatively fresh mantle xenolith from Zarnitsa and Komsomolskaya pipes we used for PTX reconstructions of mantle sections. In Zarnitsa dunites - harburgites with richterite, Phl-Ilm veins, sheared lherzolites, pyroxenites (with amphibole) and eclogites and deformed peridotites. Mg -rich Gar and Opx formed stepped P-Fe# trend, Fe- enriched Cpx with Ilm were created mostly by protkimberlites. Sub Ca garnets rarely show U spikes while Ti rich show Th, U, Ta, Nb, Zr and peaks Many minerals demonstrate Th enrichment due to carbonitites. In mantle of Komsomolskaya pipe Phl is wide spreadin periditites from lherzolites ti dunites and in eclogites. There are 6 intervals with sharp division at 5 GPa.Mg eclogites prevae in lower part while fe- enriched in middle part. The Fe# rise is detevcted in lower and upper parts of mantle section. The TRE spiderdiagrams of grnets shows U -pb subduction peaks But Cpx mainly show n Th- peak. The ages of eclogites ogive 500-600 Ma (one 1525 MA) which is much less than in Zarnitsa or Udachnaya having Proterozoic - Archean ages.
Abstract: Mantle xenolith from Komsomolskya and Zarnitsa pie were used for the reconstryctions of mantle columns beneath theses kimberlite pipes. Relatively fresh mantle xenolith from Zarnitsa and Komsomolskaya pipes we used for PTX reconstructions of mantle sections. In Zarnitsa dunites - harburgites with richterite, Phl-Ilm veins, sheared lherzolites, pyroxenites (with amphibole) and eclogites and deformed peridotites. Mg -rich Gar and Opx formed stepped P-Fe# trend, Fe- enriched Cpx with Ilm were created mostly by protkimberlites. Sub Ca garnets rarely show U spikes while Ti rich show Th, U, Ta, Nb, Zr and peaks Many minerals demonstrate Th enrichment due to carbonitites. In mantle of Komsomolskaya pipe Phl is wide spreadin periditites from lherzolites ti dunites and in eclogites. There are 6 intervals with sharp division at 5 GPa.Mg eclogites prevae in lower part while fe- enriched in middle part. The Fe# rise is detevcted in lower and upper parts of mantle section. The TRE spiderdiagrams of grnets shows U -pb subduction peaks But Cpx mainly show n Th- peak. The ages of eclogites ogive 500-600 Ma (one 1525 MA) which is much less than in Zarnitsa or Udachnaya having Proterozoic - Archean ages.
Lithos, doi 10.1016/j.lithos.2019.105215, 75p. Pdf
Europe, Spain
deposit - Ronda
Abstract: We present a detailed study of the water geochemistry, mineralogy and textures in serpentinization-related hyperalkaline springs in the Ronda peridotites. Ronda waters can be classified into hyperalkaline fluids and river waters that are broadly similar to Ca2+-OH- and Mg2+-HCO3- water types described in serpentinite-hosted alkaline springs elsewhere. At the discharge sites of the fluids (fractures or human made outlets) and ponds along the fluid flow paths, the fluids are hyperalkaline (10.9 < pH < 12) and characterized by low Mg and high Na, K, Ca, and Cl concentrations. River waters, occurring near the spring sites, are mildly alkaline (8.5 < pH < 8.9) and enriched in Mg and DIC compared to Na, K, Ca and Cl. The chemistry of Ronda Mg-HCO3 river waters is likely due to the hydrolysis of ferromagnesian peridotite minerals in equilibrium with the atmosphere by infiltrated meteoric water and shallow groundwater in the serpentinized peridotite. The Ronda Ca-OH hyperalkaline fluids are generated by the combination of low temperature serpentinization reactions from infiltrated surface Mg-HCO3 river waters —or Ca-HCO3 waters from near karst aquifers— and deep carbonate precipitation isolated from atmospheric CO2. Mass balance calculations indicate that the weathering of Ca-bearing peridotite silicates such as diopside is a feasible source of Ca in Ronda Ca-OH hyperalkaline fluids; however, it requires steady-state dissolution rates substantially greater than those determined experimentally. Travertine, crystalline crusts and sediment deposits are the main types of solid precipitates observed in Ronda hyperalkaline spring sites. Calcite and aragonite, minor dolomite and Mg-Al-rich clays are the main minerals in the spring sites. As illustrated in the Baños del Puerto spring site, (i) calcite-dominated precipitation is due to hyperalkaline fluid uptake of atmospheric CO2 during discharge, and (ii) aragonite-dominated precipitation is due to mixing of Ca-OH hyperalkaline fluids with Mg- HCO3 river waters. Aragonite and dolomite contents increase away from the springs and toward the river waters that uniquely reflects the effect of Mg ions on the precipitation of aragonite versus calcite. Other potential factors controlling the precipitation of these CaCO3 polymorphs are the Mg/Ca ratio, the CO2 content, and the temperature of the fluids. Dolomite forms during lithification of travertine due to periodic flooding of river water combined with subsequent evaporation.
Magna, T., Viladkar, S., Rappirich, V., Pour, O., Cejkova, B.
Nb-V enriched sovites of the northeastern and eastern part of the Amba Dongar carbonatite ring dike, India - a reflection of post emplacement hydrothermal overprint.
Abstract: Archean cratons are underlain by highly depleted subcontinental lithospheric mantle (SCLM). However, there are extensive evidences that Archean SCLM has been extensively refertilized by metasomatic processes, with the addition of Fe, Ca, and Al to depleted protoliths. The distribution of sub-calcic Cr-rich garnets in the SCLM beneath the Siberian craton suggests (1) sub-calcic garnets and diamonds are metasomatic phases in the cratonic SCLM; (2) the distribution of both phases is laterally heterogeneous on relatively small scales and related to ancient structural controls [1]. Re-Os isotopic compositions of twenty six sulfide inclusions in lherzolitic Cr-pyropes from Upper Muna kimberlites have been determined by laser ablation MCICPMS. Most analysed sulfides (~92%) have very low Re/Os ratios (<0.07), and their Re-depletion ages (TRD) form three major peaks: 3.4-2.8, 2.2-1.8 and 1.4-1.2 Ga (±0.03 Ga, mean 2s analytical uncertainty). One sulfide give the oldest TRD age at 4 Ga. Our data suggest that refertilization of the highly depleted SCLM and the introduction of Cr-pyrope garnet occurred in several episodes. The oldest age of ca 4 Ga indicate on the beginning of the formation of the depleted SCLM of the Siberian Craton in Hadean time [2].
Abstract: Much of our knowledge of the Earth’s deep interior comes from theoretical models, which are based on the results of experimental petrology and seismology. Diamonds in such models are the unique natural samples because they contain and preserve inclusions of mantle materials that have been entrapped during diamond growth and remained unchanged for long geologic time. In the present study for superdeep sublithospheric diamonds from Saõ-Luiz (Juina, Brazil) and northeastern Siberian Platform with mineral inclusions of the Transition Zone and Lower Mantle (majorite garnet, coesite (stishovite), ferropericlase and Mg-Si-, Ca-Si-, Ca-Ti, Ca-Si- Ti-perovskite), the diffraction of backscattered electrons technique (EBSD) revealed features of the internal structure. Superdeep diamonds are characterized by a defective and imperfect internal structure, which is associated with the processes of growth and post-growth plastic deformation. The deformation is manifested both in the form of stripes parallel to the (111) direction, and in the form of an unordered disorientation of crystal blocks up to 2°. In addition, for many crystals, a block structure was established with a greater disorientation of the sub-individuals, as well as the presence of “diamond-in-diamond” inclusions and microtwins. Additional stresses are often observed around inclusions associated with the high remaining internal pressure. It has previously been shown that the crystal structure of superdeep diamonds is significantly deformed around inclusions of perovskites, SiO2 (stishovite?), and Mg2SiO4 (ringwoodite?). The significant plastic deformations detected by the EBSD around inclusions testify to phase transitions in superdeep minerals (perovskites, stishovite, and ringwoodite) [1].
Agrosi, G., Tempesta, G., Mele, D., Caggiani, MC., Mangone, A., Della Ventura, G., Cestelli-Guidi, M., Allegretta, I., Hutchison, M.T., Nimis, P., Nestola, F.
Abstract: Super-deep diamonds and their mineral inclusions preserve very precious information about Earth’s deep mantle. In this study, we examined multiphase inclusions entrapped within a diamond from the Rio Vinte e um de Abril, São Luiz area (Juina, Brazil), using a combination of non-destructive methods. Micro-Computed X-ray Tomography (?-CXRT) was used to investigate the size, shape, distribution and X-Ray absorption of inclusions and mapping by micro X-ray Fluorescence (?-XRF), ?-Raman Spectroscopy and micro-Fourier Transform Infrared Spectroscopy (?-FTIR) were used to determine the chemical and mineralogical composition of the inclusions. Four large inclusions enclosed in the N-rich diamond core consist of dominant ferropericlase-magnesiowüstite and locally exsolved magnesioferrite. FTIR maps, obtained integrating the band at 1430 cm?1, show also the presence of carbonates. A fifth large inclusion (ca 100 ?m) was remarkable because it showed a very unusual flask shape, resembling a fluid/melt inclusion. Based on ?CXRT tomography and ?-Raman mapping, the flask-shaped inclusion is polyphase and consists of magnetite and hematite partly replacing a magnesiowüstite core and small-volume of gas/vacuum. ?-Raman spectra on the same inclusion revealed local features that are ascribed to post-spinel polymorphs, such as maohokite or xieite, which are stable at P ? 18 GPa, and to huntite, a carbonate with formula CaMg3(CO3)4. This represents the first finding of maohokite and huntite in diamond. We interpret the composition of the inclusions as evidence of formation of ferropericlase-magnesiowüstite and diamond in a carbonate-rich environment at depths corresponding at least to the Transition Zone, followed by oxidation of ferropericlase-magnesiowüstite by reaction with relatively large-volume entrapped melt during diamond ascent.
Alvaro, M., Mazzucchelli, M.L., Angel, R.J., Murri, M., Campmenosi, N., Scambelluri, M., Nestola, F., Korsakov, A., Tomilenko, A.A., Marone, F., Morana, M.
Abstract: Metamorphic rocks are the records of plate tectonic processes whose reconstruction relies on correct estimates of the pressures and temperatures (P-T) experienced by these rocks through time. Unlike chemical geothermobarometry, elastic geobarometry does not rely on chemical equilibrium between minerals, so it has the potential to provide information on overstepping of reaction boundaries and to identify other examples of non-equilibrium behavior in rocks. Here we introduce a method that exploits the anisotropy in elastic properties of minerals to determine the unique P and T of entrapment from a single inclusion in a mineral host. We apply it to preserved quartz inclusions in garnet from eclogite xenoliths hosted in Yakutian kimberlites (Russia). Our results demonstrate that quartz trapped in garnet can be preserved when the rock reaches the stability field of coesite (the high-pressure and high-temperature polymorph of quartz) at 3 GPa and 850 °C. This supports a metamorphic origin for these xenoliths and sheds light on the mechanisms of craton accretion from a subducted crustal protolith. Furthermore, we show that interpreting P and T conditions reached by a rock from the simple phase identification of key inclusion minerals can be misleading.
Yellowknife Forum NWTgeoscience.ca, abstract Volume p. 7.
Canada, Northwest Territories
deposit - Diavik
Abstract: Diavik has a robust communities portfolio to ensure that our impacted communities are informed and trusted partners in the success of our operation. The Diavik Traditional Knowledge Panel has been in place since 2012 as a resource for developing and providing recommendations on a variety of operational and closure details. The Panel is comprised of a male elder, a female elder and a youth from each of the five Participation Agreement communities and, to date, have made 194 recommendations. Diavik will present on the benefits and opportunities that are created when we utilize traditional knowledge in our operations.
Contributions to Mineralogy and Petrology, Vol. 174, 28p. Pdf
Africa, Ghana
deposit - Akwatia
Abstract: Trace-element concentrations in olivine and coexisting garnets included in diamonds from the Akwatia Mine (Ghana, West African Craton) were measured to show that olivine can provide similar information about equilibration temperature, diamond paragenesis and mantle processes as garnet. Trace-element systematics can be used to distinguish harzburgitic olivines from lherzolite ones: if Ca/Al ratios of olivine are below the mantle lherzolite trend (Ca/Al??300 µg/g Ca or?>?60 µg/g Na are lherzolitic. Conventional geothermobarometry indicates that Akwatia diamonds formed and resided close to a 39 mW/m2 conductive geotherm. A similar value can be derived from Al in olivine geothermometry, with TAl-ol ranging from 1020 to 1325 °C. Ni in garnet temperatures is on average somewhat higher (TNi-grt?=?1115-1335 °C) and the correlation between the two thermometers is weak, which may be not only due to the large uncertainties in the calibrations, but also due to disequilibrium between inclusions from the same diamond. Calcium in olivine should not be used as a geothermobarometer for harzburgitic olivines, and often gives unrealistic P-T estimates for lherzolitic olivine as well. Diamond-hosted olivine inclusions indicate growth in an extremely depleted (low Ti, Ca, Na, high Cr#) environment with no residual clinopyroxene. They are distinct from olivines from mantle xenoliths which show higher, more variable Ti contents and lower Cr#. Hence, most olivine inclusions in Akwatia diamonds escaped the refertilisation processes that have affected most mantle xenoliths. Lherzolitic inclusions are probably the result of refertilisation after undergoing high-degree melting first. Trivalent cations appear to behave differently in harzburgitic diamond-hosted olivine inclusions than lherzolitic inclusions and olivine from mantle xenoliths. Some divalent chromium is predicted to be present in most olivine inclusions, which may explain high concentrations up to 0.16 wt% Cr2O3 observed in some diamond inclusions. Strong heterogeneity of Cr, V and Al in several inclusions may also result in apparent high Cr contents, and is probably due to late-stage processes during exhumation. However, in general, diamond-hosted olivine inclusions have lower Cr and V than expected compared to mantle xenoliths. Reduced Na activity in depleted harzburgites limits the uptake of Cr, V and Sc via Na-M3+ exchange. In contrast, Al partitioning in harzburgites is not significantly reduced compared to lherzolites, presumably due to uptake of Al in olivine by Al-Al exchange.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 57.
Canada, Northwest Territories
deposit - Gahcho Kue
Abstract: Gahcho Kué Mine is owned as a joint venture between Mountain Province Diamonds Inc. and De Beers Canada Inc. Located about 280 km northeast of Yellowknife, it is Canada’s newest diamond mine and the world’s largest in the last 14 years. After two years of construction, commercial operations began in September 2016. As the mine enters into its fourth year of operation, De Beers is pleased to provide an update on the current mine operations, updated mine plan, safety, environment, and social performance.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 90.
Canada, Northwest Territories
deposit - Diavik
Abstract: Diavik’s newest orebody, the A21 kimberlite pipe, was brought into production in December 2017 when surface mining began. This is the fourth kimberlite pipe to be mined at the Diavik Diamond Mine, located at Lac de Gras, 300 kilometres northeast of Yellowknife. To access this underwater orebody, Diavik constructed an engineered, 2.1 km long rock fill water retention dike during 2014 to 2017. This has now opened up the opportunity to study and evaluate possible mining methods below the open pit. Such additional kimberlite extraction would occur from 2023 to 2025.
Yellowknife Forum NWTgeoscience.ca, abstract volume p.69.
Canada, Northwest Territories
deposit - Snap Lake
Abstract: The Snap Lake Mine is a former underground diamond mine operated by De Beers Canada Inc.( De Beers), located about 220 km northeast of Yellowknife in the Northwest Territories. The Snap Lake Mine operated from 2008 to 2015 and De Beers submitted the Final Closure and Reclamation Plan for the mine. The mine is currently in it fourth year of being managed in a state of Extended Care and Maintenance (ECM). Activities during ECM include monitoring of water quality and other environmental parameters, collecting and treating effluent and making sure that water leaving the site meets water license requirements. Physical infrastructure such as the airstrip, roadways, buildings, processed kimberlite containment facilities and associated surface water infrastructure such as pumps, sumps and channels need to be kept in a safe and operable condition. After a trail-run of reduced camp occupancy in 2017, the site was fully winterized and demobilized in September 2018. This update will review the first seasonal zero occupancy at Snap Lake, as well as the work completed in spring/summer of 2019.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 70.
Canada, Northwest Territories
deposit - Snap Lake
Abstract: The Snap Lake Mine is a former underground diamond mine operated by De Beers Canada Inc. (De Beers), located about 220 km northeast of Yellowknife in the Northwest Territories. The Snap Lake mine operated from 2008 to 2015, and entered a Care and Maintenance mode in December 2015. The mine is currently entering its fourth year of being managed in this Extended Care and Maintenance phase. In order to ensure continual remote monitoring of certain key geotechnical, meteorological and air quality instrumentation and to enable visual observation of key infrastructure, work was done in 2018 to integrate new and existing monitoring instrumentation into the existing Campbell Scientific PakBus network. In this presentation De Beers will share a summary of this work, with the emphasis on the type of technology, detail of installation and integration of systems between the various pieces of instrumentation. First we will discuss installation of the 5 data collection stations that relay geotechnical instrumentation information. The data collection system at each of the 5 stations consists of a solar panel, battery, data logger, multiplexor and short-wave radio. To enable redundancy, a manual data collection via USB was added, in the event that remote communication with the stations is lost. Second, an overview of the installation of camera monitoring stations as well as the communications protocol used for the integration of the weather and ambient air quality data transmitted via satellite will be presented. While the focus will be on the technology and systems used for remote monitoring, and not the actual monitoring results per se, it is our intention to share this and some of the successes and challenges experienced during the first year of remote monitoring during zero occupancy conditions.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 71-72.
Canada, Nunavut
deposit - Chidliak
Abstract: The Chidliak exploration site was discovered in 2005 and acquired by De Beers Canada (De Beers) in September 2018. The Project is located on the Hall Peninsula of Baffin Island in the Qikiqtani Region of Nunavut and the closest communities are the Hamlet of Pangnirtung and the City of Iqaluit. The current Chidliak exploration site is not located within Inuit Owned Lands, Territorial or National Parks and is located entirely within Crown Lands. The current Chidliak exploration site includes 30 kimberlites two of which (CH-06 and CH-07) have been tested for grade and diamond value and are considered to be at an Inferred level of resource confidence. De Beers is currently engaged in a concept study to evaluate various FutureSmart Mining methods that would minimize environment impacts and enable relatively small kimberlites (diamond bearing rock) to be mined. De Beers is conducting desktop and field studies to evaluate options for mining methods, infrastructure, processing, information technology, and employee work models. In parallel, environmental field programs were conducted in 2019 to advance the environmental data collected in 2009 to 2017 and to support the evaluation of mining options. This presentation will provide a brief synopsis of the Project and work conducted in 2019 to advance the Project.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 72.
Canada, Northwest Territories
deposit - Snap Lake
Abstract: The Snap Lake Mine (the Mine) is a former underground diamond mine operated by De Beers Canada (De Beers), located about 220 kilometres northeast of Yellowknife in the Northwest Territories. The Snap Lake Mine operated from 2008 to 2015, and entered a Care and Maintenance mode in December 2015. In February 2017, the Mine underground workings were decommissioned and allowed to flood, in December 2017, De Beers announced the intent to enter into final closure, and in March 2019, De Beers submitted the Final Closure and Reclamation Plan for the Mine. Water management has always been an important component at the Mine and was considered in development of the Final Closure Plan to achieve the overall goal of “returning the site and affected areas around the Mine to technically viable and, where practicable, self-sustaining ecosystems that are compatible with a healthy environment and with human activities”. Water management at the Mine has changed significantly since diamond mining operations ceased. During diamond mining operations, a large volume of water was pumped from the underground to the surface for management and release to Snap Lake and the downstream environment. This mine water was relatively high in total dissolved solids and total suspended solids and therefore had to be treated prior to discharge. Now that the underground is flooded, there is no longer a need to pump mine water to the surface and water management has been greatly simplified. Since 2017, small volumes of runoff water from the North Pile (a surface disposal facility that was used for processed kimberlite, waste rock, and non-hazardous solid waste during operations) is collected for management and release to the underground and to Snap Lake. Water quality and aquatic ecosystem monitoring has been conducted yearly since pre-mining. Results of these programs have informed adaptive management at the site and informed plans for closure. The focus of this presentation is on water management and monitoring, for the Mine to the receiving environment, covering the history of the Mine to present and into planning for closure.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 85.
Canada, Northwest Territories
deposit - Gahcho Kue
Abstract: A vegetation and soils monitoring program was implemented at the Gahcho Kué Mine to test for mine-related changes to vegetation and soils from dust deposition. Besides measuring changes in vegetation and soils, one objective of the study is to inform the Wildlife Effects Monitoring Program with respect to the potential for dust as a mechanism for avoidance of habitats near the Mine by caribou and other wildlife. Soil properties, plant communities, and dust deposition have been monitored since 2013 with permanent vegetation plots and dust collectors using a gradient study design prior to and during construction and operation of the Mine. A single study area transect was established in a west-southwest direction extending 20 kilometres from the Mine footprint, which was based on the prevailing wind direction and terrain features (i.e., large lakes), and the distribution of the target plant community across the landscape. Dustfall deposition and associated metals concentrations, and soil moisture and temperature variables are monitored annually. Data on plant species richness and abundance and soil pH and salinity are collected every three years. Analysis of variance was performed to determine if fixed dustfall deposition rates varied among sampling areas, seasons, and years. A repeated measures analysis of variance was used to examine patterns of species abundance (percent cover) and species richness across sampling areas and years. Although dust deposition has shown increasing trends since the commencement of construction and operation, no effects on vegetation from dust were observed in the current analysis. Metals concentrations in dust were generally below detection limits or in trace amounts, consistent with baseline values, and soil pH and salinity were within baseline values. Minor observed changes in species richness are likely related to natural variation in site conditions among vegetation plots and associated sampling areas, annual variation in climate, surveyor variability, and foraging by caribou and other wildlife. Differences in annual dust deposition rates may be attributed to annual variations in temperature, wind, and rainfall. The results suggest that dust-related changes in vegetation community composition is likely not a factor influencing the avoidance of habitats near the Mine by caribou or other wildlife.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 89-90.
Canada, Northwest Territories
deposit - lac de Gras
Abstract: Till dispersal patterns may appear as a consistent train of indicators extending in the direction of the latest ice-flow phase from a source, or along a direction defined by an older ice-flow phase. However, other dispersal patterns, sometimes even in the same area, may have poorly-defined, discontinuous trains, or even lack dispersal trains all together. This research investigates dispersal patterns from two sites southeast of Lac de Gras that were affected by the same ice-flow history, but show important differences in bedrock topography, till thickness, and subglacial landform assemblages. The goal is to improve our understanding of bedrock and till thickness effects on dispersal trains. New local ice-flow indicators (n=16) constrain local ice-flow history. Digital elevation models and a surficial map are used to identify surficial landforms and to loosely constrain bedrock topography. We also use a subset of KIM results from a large industry-donated RC-drilling database (n=502 from 185 boreholes) which includes information on subsurface sediment characteristics and depth-to-bedrock data, which further constrain bedrock topography. In addition, we use texture, matrix geochemistry, KIMs, and clast lithology from a smaller set of 51 surface samples to compare dispersal patterns at surface and at depth. Part of the eastern study area is characterized by a well-defined drumlin field associated with the young NW ice-flow phase, variable till thickness (0-18m), and relatively flat bedrock topography (<20m elevation change). Kimberlites WO-17/WO-20 exhibit a short, but well-defined KIM dispersal train in the direction of the last dominant flow phase (NW); the dispersal area is also characterized by thin discontinuous till. A second KIM dispersal train is also recognized in the thicker till of the drumlin field SW of WO-17/20. Based on its location relative to WO-17/20, and till geochemistry and lithology counts, this pattern is interpreted to be a palimpsest train associated to the oldest SW ice flow. The western study area, located 20km from the eastern area, is characterized by a similar ice-flow history, but its bedrock topography varies more (~70m), with thin till, generally under 4m. A known kimberlite within the western area (Big Blue) is nestled within a bedrock topographic high ~20m above the surrounding terrain. Fragmented and more elusive till anomalies occur down-ice from this source. The lack of a well-developed dispersal train associated with the kimberlite is noteworthy, and may be due to the evolution of subglacial conditions around the bedrock hill. Our current model involves initial basal sliding and erosion of the top of the kimberlite and englacial entrainment. This phase was followed by reduced local abrasion and erosion rates within the kimberlite depression, possibly related to the development of low-pressure cavities over several local depressions: an idea supported by evidence of late-stage meltwater activity. This research highlights the important role of bedrock topography and related subglacial conditions both in the source area and dispersal area, as well as the potential for enhanced preservation of palimpsest trains in drumlinized till blankets.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 95-96.
Canada, Northwest Territories
deposit - Ekati
Abstract: The Ekati Diamond Mine is a surface and underground diamond mine operated by Dominion Diamond Mines. It is located near Lac de Gras within the Northwest Territories, Canada approximately 300 km north of Yellowknife and roughly 200 km south of the Arctic Circle. The Long Lake Containment Facility (LLCF) is the primary containment area for processed kimberlite (PK) storage after the extraction of diamonds from kimberlite ore. The facility has been in operation since 1998 and is the main repository of PK from open pit and underground mines at the Ekati Mine. The overall reclamation goal for the LLCF is the design and construction of a long-term cover that will physically stabilize the PK, with a landscape that will be safe for human and wildlife use. The proposed final closure design for the LLCF includes the following components: 1) Combination of vegetation and rock cover system to physically stabilize the PK. Vegetation is planned to be the main stabilization component of the PK. Rock placement is intended to promote a localized environment for vegetation growth and provide larger-scale wind and water erosion protection. 2) Water drainage channels to convey surface water flow through the containment cells and into settling ponds. Since 2012, reclamation research has been ongoing at Cell B of the LLCF with the overall intent of addressing uncertainties with the proposed final LLCF cover design. Separate reclamation research programs focused on addressing the uncertainties of vegetation growth in PK are being carried out under this project. Dominion’s short-term research goal has been to establish and evaluate the vegetation growth directly within PK. Main components of the LLCF reclamation research includes evaluation of soil amendments, rock/vegetation combinations, annual crop cover, plant species trials, mine-generated organic matter application, seed collection/distribution, and natural vegetation colonization. The LLCF reclamation research aims to establish a best practice that could be adapted by other mining operations looking to reclaim PK containment sites. Annual vegetation monitoring and continued program expansion aid in reaching that goal. Recent program undertakings have included: 1)Surface water management research through trial channel construction and further bio-engineering of existing channels 2) Mycorrhizae inoculation to improve soil microbial communities 3) Implementation of rough and loose mounding as an erosion control measure 4) Evaluation of the feasibility of using organic matter generated from the Ekati composter facility 5) Harvesting of halophytic seed and live plant specimens from saline environments near Kugluktuk, Nunavut for planting in Cell B 6) Utilization of reclamation equipment for earthworks. The LLCF reclamation research has been a vessel for developing methods of utilizing PK as an effective growth medium. High sodium concentrations and low organic matter content present challenges, but also provide opportunities for innovative research to improve environmental conditions and lead to a final closure design. Dominion has included Traditional Knowledge, other scientific knowledge, as well as regulatory and community input as a key component of LLCF reclamation research planning and final cover design.
Yellowknife Forum NWTgeoscience.ca, abstract volume poster p. 123-124.
Canada, Northwest Territories
deposit - Kelvin
Abstract: Research at the Kelvin kimberlite, NWT, is defining surface exploration practices and testing new host rock lithogeochemical exploration tools that will result in reduced costs and improved discovery success. In regions where recent glaciation has buried kimberlites under glacial sediments, surface geochemical detection methods are best interpreted when coupled with a comprehension of the landscape formation processes. The glacial, post-glacial, and cryoturbation processes that have affected the landscape have, in turn, affected the dispersal of geochemical signatures in the till that can be detected and exploited by detailed surface mapping, sampling, and geochemical analysis. The Kelvin kimberlite is an inclined pipe that subcrops from metaturbidite country rock beneath a lake. No indicator mineral train has been detected at Kelvin by traditional indicator mineral methods. Relative uniformity of surficial material (<6m thick till blanket) allows for extensive B horizon soil sampling above the kimberlite, up-ice, and up to 1 km down-ice. Four acid and aqua regia ICP-MS results of the -180 ?m fraction indicate the presence of subtle pathfinder element trains originating from the kimberlite subcrop location and extending for >1km down-ice. Dry sonic sieving and four acid digestion results provide interpretations of geochemical partitioning and the ideal size fraction for geochemical sampling. Trace elements demonstrate systematically elevated concentrations in the fine and very fine silt fractions; however, background is higher and anomalous to background contrast is not enhanced compared to bulk -180 ?m ratios. Elevated pathfinder concentrations in the fine to very fine sand fraction are attributed to fine kimberlite indicator minerals and their fragments, and display the best anomalous to background contrast ratio. Whole soil commercial Pb isotope analysis of select soils provide supplemental data to fingerprint the petrogenetic source of anomalous samples. Additional research is being carried out to detect alteration signatures in the country rock induced by the emplacement of the kimberlite. Lithogeochemical data from four drill holes aims to identify and quantify the metasomatic enrichment and depletion of elements sourced from the kimberlite, while hyperspectral imaging will aim to detect secondary mineralogy and subtle changes in mineral composition. This data will be used to generate mineralogical and geochemical vectors beneficial in near-miss situations when drilling kimberlites and defining diatreme geometries.
Abstract: The so-called rift/graben of Asunción was formed in the central-northern portion of the Archon lithospheric nucleus of the Rio de la Plata craton. This structure, related to a crustal thinning, likely resulted from an extraterrestrial impact which produced the San Miguel impact crater. The impact structure is located immediately to the south of the Asunción rift/graben. Within the central E-W segment of the rift/graben and in association with other igneous rocks (potasic to ultra-potasic) of around 130-125 Ma, the picritic rock pipe with lamprofidic texture Ymi-1 occurs. This pipe is found in the lower region of this rift/graben through faults (depths of up to -3000 m). Rocks of a plug and a dike exposed in the pipe Ymi-1 show that it is a strongly porphyritic rock with tendencies of lamprophiric texture formed by micro-feno crystals and mega-crystals of forsteritic olivine (>10 to 30% modal); mega-phenocrysts of Ti-Al diopside and micro-phenocrysts of chromite (Mg-chromite poor in Ti and Mg-Ti chromite); they are supported by an inter-granular matrix formed by aluminosus diopside, Al-Ti-phlogopite/biotite, Mg-Ti-magnetite, amphiboles (hornblends, eckernmanite together with some other potassium to sodic titaniferous amphiboles) accompanied by sanidine, analcime and traces of plagioclase (poor in An molecules). The mineral chemistry of spinels, phlogopites/biotites and diopsids are strongly compatible with mineral chemistry known in calc-alkaline lamprophyres. The rock chemistry of one available dyke is also compatible with the chemistry of calc-alkaline lamprophyres.Ymi-1 is a calc-alkaline picritic lamprophyre pipe where the study of the chromite (50-57 % Cr2O3) type and frosting-tourmaline ("dravites"), obtained in rock and in heavy mineral concentrates (in volcano-epiclastic sediments and in stream sediments -collected in its bed) suggest that it would be a diamond-bearing lamprophyre. The presence of diamonds was confirmed (by X-rays and other methods) in the Ymi-1 pipe. 1D S-wave seismic profile of continental data, for the pipe Ymi-1 site, suggests a geothermal gradient between 38.5 to 39 mW/m2, thus the Ymi-1 calc-alkaline lamprophyre an attractive target for an eventual diamond deposit. Supplementary materials S1 - PDF (Figuras suplementarias) S2 - PDF (Geoquímica mineral) https://pyflow.net/joomla30/index.php/9-all-issues/38-el-lamprofido-picritico-con-diamantes-ymi-1.
Abstract: Kimberlites are complex, ‘hybrid’ igneous rocks because their parental magmas entrain abundant crust- and mantle-derived components that can be readily assimilated during ascent to surface. Recent studies of olivine zonation patterns have shown compositional relationships between xenocrystic cores and magmatic rims, suggesting that kimberlite melt compositions might be controlled by assimilation of mantle material during emplacement. However, the nature and extent to which this process, as well as assimilation of crustal material, influences melt compositions within single kimberlite fields remains unclear. To address this issue, we have conducted a comprehensive geochemical and petrographic investigation of kimberlites from eight pipes in the Kaavi-Kuopio field in Finland, which were emplaced on the southern margin of the Karelian craton during the Neoproterozoic (~550-600 Ma). While magmatic olivine rims are usually homogeneous in composition within and between kimberlites of a single cluster and field (e.g., Lac de Gras), the Kaavi-Kuopio kimberlites appear to represent a unique case where there are statistically significant differences between the average Mg# of olivine rims in different pipes (89.9 ± 0.2 to 88.5 ± 0.3). Importantly, the Mg# of magmatic olivine rims exhibit a strong correlation with the Mg# of their mantle-derived xenocrystic cores. Furthermore, the compositions of olivine cores and rims exhibit a robust relationship with those of magmatic spinel (e.g., Mg#, TiO2 contents). These geochemical variations also align with the mineralogy of the kimberlites: whereby abundances of phlogopite and oxides (e.g., spinel) are negatively correlated with olivine rim Mg#. The robust relationship between entrained and assimilated lithospheric mantle material (i.e. olivine cores) and magmatic components (i.e. olivine rims, spinel, and groundmass mineral abundance), combined with numerical modelling suggests that up to 10 wt% assimilation of lithospheric mantle material has modified the compositions of the Kaavi-Kuopio kimberlites. These new data are also consistent with significant variations in the lithospheric mantle composition of the Karelian craton beneath the closely spaced (<10 km) kimberlites. Finally, in addition to mantle assimilation, formation of Si-Fe-rich mica in some of the examined kimberlites might be linked to late-stage increases in oxygen fugacity potentially enhanced by crustal contamination. This study shows for the first time that variable assimilation of mantle and crustal material can generate significant variations in kimberlites derived from seemingly similar sources.
Journal of Petrology, in press available, 79p. Pdf
Europe, Finland
deposit - Kuusamo
Abstract: Kimberlites are often closely associated, both in time and space, with a wide variety of alkaline ultramafic rock types; yet the question of a genetic relationship between these rock types remains uncertain. One locality where these relationships can be studied within the same cluster is the Karelian craton in Finland. In this study we present the first petrographic, mineral and whole-rock geochemical results for the most recently discovered kimberlite cluster on this craton, which represents an example of the close spatial overlap of kimberlites with ultramafic lamprophyres. The Kuusamo cluster incorporates seven bodies (Kasma 45, Kasma 45 south, Kasma 47, Kalettomanpuro (KP), Kattaisenvaara (KV), Dike 15 and Lampi) distributed along a 60?km NE-SW corridor. Hypabyssal samples from KV, KP, Kasma 45 and Kasma 47 consist of altered olivine macrocrysts and microcrysts and phlogopite phenocrysts in a groundmass of perovskite, apatite, spinel, ilmenite, serpentine, and calcite. These petrographic features combined with mineral (e.g., Mg-rich ilmenite, Al-Ba-rich, Ti-Fe-poor mica) and whole-rock incompatible trace element compositions (La/Nb = 0.8 ± 0.1; Th/Nb = 0.07 ± 0.01; Nb/U = 66 ± 9) are consistent with these rocks being classified as archetypal kimberlites. These Kuusamo kimberlites are enriched in CaO and poor in MgO, which combined with the absence of chromite and paucity of olivine macrocrysts and mantle-derived xenocrysts (including diamonds), suggest derivation from differentiated magmas after crystal fractionation. Samples from Lampi share similar petrographic features, but contain mica with compositions ranging from kimberlitic (Ba-Al-rich cores) to those more typical of orangeites/lamproites (increasing Si-Fe, decreasing Al-Ti-Ba), and have higher bulk-rock SiO2 contents than the Kuusamo kimberlites. These features, combined with the occurrence of quartz and titanite in the groundmass, indicate derivation from a kimberlite magma that underwent considerable crustal contamination. This study shows that crustal contamination can modify kimberlites by introducing features typical of alkaline ultramafic rock types. Dike 15 represents a distinct carbonate-rich lithology dominated by phlogopite over olivine, with lesser amounts of titaniferous clinopyroxene and manganoan ilmenite. Phlogopite (Fe-Ti-rich) and spinel (high Fe2+/Fe2++Mg) compositions are also distinct from the other Kuusamo intrusions. The petrographic and geochemical features of Dike 15 are typical of ultramafic lamprophyres, specifically, aillikites. Rb-Sr dating of phlogopite in Dike 15 yields an age of 1178.8 ± 4.1?Ma (2?), which is considerably older than the ?750?Ma emplacement age of the Kuusamo kimberlites. This new age indicates significant temporal overlap with the Lentiira-Kuhmo-Kostomuksha olivine lamproites emplaced ?100?km to the southeast. It is suggested that asthenospheric aillikite magmas similar to Dike 15 evolved to compositions akin to the Karelian orangeites and olivine lamproites through interaction with and assimilation of MARID-like, enriched subcontinental lithospheric mantle. We conclude that the spatial coincidence of the Kuusamo kimberlites and Dike 15 is likely the result of exploitation of similar trans-lithospheric corridors.
Brazil Journal of Geology ( www.scielo.br) ENG, 15p. Pdf
South America, Brazil
deposit - Parana
Abstract: The Paraná deposit, located at Southwestern Rio Grande do Norte state, in Brazil, is one of the few emerald deposits found at Borborema Province. The mineralization occurs in phlogopite schists and actinolite-phlogopite schists associated with pegmatites and albitites within the Portalegre Shear Zone. Unlike other well-known Brazilian emerald deposits, the mineralogy of Paraná emeralds has remained poorly investigated for the last 40 years. In this study, we conducted mineralogical characterization of theses emeralds through gemological testing, mineral chemistry, absorption and reflectance spectroscopy, and thermal analysis. The Paraná emeralds are bluish-green colored, characterized by high refractive index, several two-phase fluid inclusions and mica is the main mineral inclusion. Electron probe microanalysis and laser ablation-inductively coupled plasma-mass spectrometry analyses detected the presence of Fe2+ (0.43-1.94 wt.% FeO) and Cr3+ (0.04-0.14 wt.% Cr2O3) as the main chromophores replacing octahedral Al3+ in the crystal structure. In addition, substantial amounts of MgO (0.40-2.72 wt.%), Na2O (0.50-1.81 wt.%), and Cs2O (0.07-0.44 wt.%) were also identified. The main causes for its coloration were attributed to Cr3+ absorption features in visible spectral range, which were corroborated by absorption and reflectance spectra. The presence of types I and II H2O at channel-sites was recorded in Fourier-transform infrared spectra and demonstrated by dehydration processes observed in different thermal and thermogravimetric analyses.
Contributions to Mineralogy and Petrology, Vol. 174, (12) doi: 10.1007/s00410-019-1634-y
Africa, Ghana
deposit - Akwatia
Abstract: Trace-element concentrations in olivine and coexisting garnets included in diamonds from the Akwatia Mine (Ghana, West African Craton) were measured to show that olivine can provide similar information about equilibration temperature, diamond paragenesis and mantle processes as garnet. Trace-element systematics can be used to distinguish harzburgitic olivines from lherzolite ones: if Ca/Al ratios of olivine are below the mantle lherzolite trend (Ca/Al??300 µg/g Ca or?>?60 µg/g Na are lherzolitic. Conventional geothermobarometry indicates that Akwatia diamonds formed and resided close to a 39 mW/m2 conductive geotherm. A similar value can be derived from Al in olivine geothermometry, with TAl-ol ranging from 1020 to 1325 °C. Ni in garnet temperatures is on average somewhat higher (TNi-grt?=?1115-1335 °C) and the correlation between the two thermometers is weak, which may be not only due to the large uncertainties in the calibrations, but also due to disequilibrium between inclusions from the same diamond. Calcium in olivine should not be used as a geothermobarometer for harzburgitic olivines, and often gives unrealistic P-T estimates for lherzolitic olivine as well. Diamond-hosted olivine inclusions indicate growth in an extremely depleted (low Ti, Ca, Na, high Cr#) environment with no residual clinopyroxene. They are distinct from olivines from mantle xenoliths which show higher, more variable Ti contents and lower Cr#. Hence, most olivine inclusions in Akwatia diamonds escaped the refertilisation processes that have affected most mantle xenoliths. Lherzolitic inclusions are probably the result of refertilisation after undergoing high-degree melting first. Trivalent cations appear to behave differently in harzburgitic diamond-hosted olivine inclusions than lherzolitic inclusions and olivine from mantle xenoliths. Some divalent chromium is predicted to be present in most olivine inclusions, which may explain high concentrations up to 0.16 wt% Cr2O3 observed in some diamond inclusions. Strong heterogeneity of Cr, V and Al in several inclusions may also result in apparent high Cr contents, and is probably due to late-stage processes during exhumation. However, in general, diamond-hosted olivine inclusions have lower Cr and V than expected compared to mantle xenoliths. Reduced Na activity in depleted harzburgites limits the uptake of Cr, V and Sc via Na-M3+ exchange. In contrast, Al partitioning in harzburgites is not significantly reduced compared to lherzolites, presumably due to uptake of Al in olivine by Al-Al exchange.
Brazil Journal of Geology ( www.scielo.br) ENG, 17p. Pdf
South America, Brazil
deposit - Tres Estradas
Abstract: Carbonatites were recently discovered in Southern Brazil, which increased the interest to evaluate the economic potential of these uncommon rocks, especially the Três Estradas Carbonatite. Carbonates are the dominant minerals of fresh rock followed by apatite, but the weathering process makes apatite abundant. We focused on apatite from the carbonatite using conventional petrography and electronic microscopy associated with microprobe, micro-Raman and Fourier-transform infrared spectroscopy. Results demonstrate the existence of four types. The primary type is associated with the rock crystallization and the subsequent three others are associated with weathering processes. The alteration mechanism was favorable for initial carbonate leaching and subsequent increase of phosphate with late precipitation of three new apatite generations. The deduced model involves long exposure during polycyclic climate changes, intercalating periods of warm dry with humid climate. The apatite types differ chemically and morphologically and have distinctive characteristics that are suitable to be used to differentiate them. These properties should be considered in future planes of industrial processes to transform apatite into single superphosphate, a basic input for fertilizer production.
Abstract: The article by Abersteiner et al., (2018) discussing the mantle origin of salts in serpentine-free kimberlites from the Udachnaya-East pipe contradicts the views of Kostrovitsky et al. (2013) concerning the origin of these salts from a surface source of brines. Here we wish to emphasize that Abersteiner et al. (2018) have presented erroneous statements regarding the genesis of these rocks. On the basis of the data collected by hydrogeologists working at Udachnaya-East we consider that unaltered kimberlites occur at 400-500 m depth, where the brines precipitated salts. The relation of unaltered kimberlites to the surface sources of salt is illustrated by the cross sections of the Mir and International’naya pipes, where serpentine-free kimberlites occur at the depths of Cambrian evaporite host rocks intercalated with thick halite layers. It is assumed that the salts from surface sources prevented olivine serpentinization. The secondary origin of salts in serpentine-free kimberlites is confirmed by our investigations and the hypothesis regarding the mantle origin of salts is doubtful.
Diamonds & Related Materials, Vol. 101, 107642, 8p. Pdf
Canada, Northwest Territories
deposit - Ekati
Abstract: High pressure high temperature (HPHT) treatment has long been applied in the gem trade for changing the body colour of diamonds. The identification of HPHT-treated diamonds is a field of on-going research in gemological laboratories, as different parameters of treatment will result in either the creation or the destruction of a variety of lattice defects in diamonds. Some features that exist in treated diamonds can also be found in natural diamonds, and consequently must not be employed for the separation of treated and natural diamonds. In this research, we investigated the properties of 11 natural yellow diamonds (directly obtained from the Ekati Diamond Mine to ensure that they are untreated) before and after HPHT treatment, conducted at a temperature of 2100 °C and a pressure of 6 GPa for 10 min. We report spectroscopic data and fluorescence characteristics, collected using PL mapping, FTIR mapping and fluorescence imaging showing the distribution of lattice defects and internal growth structures. PL mapping indicates SiV defects exist in one of the nitrogen-rich natural diamonds prior to treatment. Silicon-related defects can also be created by HPHT treatment, and they seem to show a relationship with pre-existing NV? centres. SIMS analysis was conducted to confirm the presence of silicon in these diamonds. The increase in the hydrogen-related infrared absorption peak at 3107 cm?1 (VN3H) is very strong in some diamonds that do not form B-centres during treatment. NVH was observed in our HPHT-treated natural diamonds, so it is possible that this strong increase in VN3H suppresses the aggregation of A- to B-centres as the newly formed A-centres were captured by NVH lattice defects to form VN3H. HPHT-altered and HPHT-induced platelet peaks are different from their natural counterparts in peak width and shape. Strong green fluorescence over a large area of a diamond, which is linked to relatively high concentration of H3 centres, was produced after HPHT treatment. We are confident that the unusual platelet peaks and strong emission of H3 centres are reliable indicators for HPHT-treated diamonds as they are not observed in untreated natural diamonds.
Physics and Chemistry of Minerals, Vol. 47, 4, 7p. Pdf
Russia, Siberia
deposit - Khololmolokh
Abstract: In recent years, despite significant progress in the development of new methods for the synthesis of diamond crystals and in their post-growth treatment, many questions remain unclear about the conditions for the formation and degradation of aggregate impurity nitrogen forms. Meanwhile, they are very important for understanding (evaluating) the origin, age, and post-growth conditions of natural diamonds. In the present work, an attempt was made to analyze the causes of the formation of high concentrations of N3V centers in natural IaB-type diamonds from the Kholomolokh placer (the Northeast Siberian craton). The possibility of decay of B centers during the plastic deformation of diamonds is analyzed and experiments on the high-temperature annealing of diamonds containing B centers are reported. The formation of N3V centers during the destruction of the B centers at high-pressure annealing of crystals has been established by experiment. It is assumed that, in the post-growth period, diamond crystals were exposed to tectono-thermal stages of raising the superplumes of the Earth's crust of the Siberian craton.
Brazil Journal of Geology ( www.scielo.br) ENG, 14p. Pdf
South America, Brazil
deposit - Fazenda Bonfim
Abstract: The Fazenda Bonfim emerald deposit lies within the Seridó Belt. It is a classic example of deposit formed through metasomatic interactions between Be-rich granite intrusions and Cr(± V)-rich mafic-ultramafic rocks. The setting of the emerald mineralization was built under strong strike-slip dynamics, which produced serpentinization and talcification of mafic-ultramafic host-rocks, and was followed by syn-kinematic emplacement of Be-rich albite granite, favoring hydrothermal/metasomatic processes. The structural control and lithological-contrast were fundamental to the fluid flow and the best ore-shoot geometry, developed in the S-foliation intra-plane at the contact zone (phlogopite hornfels) between mafic-ultramafic rocks and the albite granite. Subsequently, an albitization process, linked to the final-stage of magmatic crystallization, led to an overall mineralogical and chemical change of the albite granite. 207U-235Pb data revealed inheritance ages from Archean to Neoproterozoic and a crystallization age of 561 ± 4 Ma for albite granite. However, 40Ar/39Ar data revealed plateau age of 553 ± 4 Ma for phlogopite hornfels, interpreted as the closure time for the metasomatic event responsible for the nucleation and growth of emerald crystals. The short interval of time between U-Pb and Ar-Ar data indicates an intense, but not protracted, metasomatic history, probably due to low volume of intrusive magma.
Abstract: Elucidating the composition of primary kimberlite melts is essential to understanding the nature of their source, petrogenesis, rheology, transport and ultimately the origin of diamonds. Kimberlite rocks are typically comprised of abundant olivine (~2560 vol%), which occurs as individual grains of variable size and morphology, and includes xenocrysts and zoned phenocrysts. Zoning patterns and inclusions in olivine can be used to decipher the petrogenetic history of kimberlites, starting from their generation in the mantle through to emplacement in the crust. This study examines well-preserved, euhedral, zoned olivine crystals from the Mark kimberlite (Lac de Gras, Canada). Olivine typically consists of xenocrystic cores, which are homogeneous in composition but vary widely between grains (Fo88.193.6). These cores are in turn surrounded by (in order of crystallisation) magmatic rims and Mg-rich rinds (Fo95.398.1). In addition, we document a new type of olivine zone (‘outmost rind’) that overgrows Mg-rich rinds. Crystal and melt/fluid inclusions are abundant in olivine and preserve a record of kimberlite melt evolution. For the first time in the studies of kimberlite olivine, we report primary melt inclusions hosted in Mg-rich olivine rinds. In addition, we observe that pseudosecondary melt/fluid inclusions are restricted to interior olivine zones (cores, rims) and are considered to have formed prior to rind formation. Pseudosecondary melt/fluid inclusions are inferred to have been entrapped at depth, as evidenced by measured densities in thermometric experiments of CO2 and decrepitation haloes, indicating a minimum entrapment pressure of ~200450 MPa (or ~615 km). Both primary and pseudosecondary melt inclusions in olivine have daughter minerals dominated by CaMg and K-Na-Ba-Sr-bearing carbonates, K-Na-chlorides along with subordinate silicates (e.g., phlogopite, monticellite), Fe-Mg-Al-Ti-spinel, perovskite, phosphates and sulphates/sulphides and periclase. In addition to phases reported in primary melt inclusions, pseudosecondary melt inclusions contain more diverse and exotic daughter mineral assemblages, where they contain phases such as tetraferriphlogopite Ba- or K-sulphates, kalsilite and Na-phosphates. The daughter mineral assemblages are consistent with a silica-poor, alkali dolomitic carbonatite melt. We demonstrate that the different types of inclusions in olivine can assist in constraining the timing of multi-stage olivine growth and the composition of the crystallising melt. The large variance in olivine zoning patterns, morphologies and Ni distribution (i.e. both coupling with and decoupling from Fo) indicates that olivine in the studied Mark kimberlite samples represent an accumulation of olivine, where olivine was derived from successive stages of the ascending magma and/or from multiple, but related pulses of magma. Primary and pseudosecondary melt/fluid inclusions in olivine indicate that a variably differentiated silica-poor, halogen-bearing, alkali-dolomitic melt crystallised and transported olivine in the Mark kimberlite.
Mineralogy and Petrology, in press available 13p. Pdf
Canada, Northwest Territories
deposit - Chidliak, Ekati
Abstract: Yellow diamonds from the CH-7 (Chidliak) and the Misery (Ekati Mine) kimberlites in northern Canada are characterised for their nitrogen characteristics, visible light absorption, internal growth textures, and carbon isotope compositions. The diamonds are generally nitrogen-rich, with median N contents of 1230 (CH-7) and 1030 at.ppm (Misery). Normally a rare feature in natural diamonds, single substitutional nitrogen (C centres) and related features are detected in infrared absorption spectra of 64% of the studied diamonds from CH-7 and 87% from Misery and are considered as the major factor responsible for their yellow colouration. Episodically grown diamonds, characterised by colourless cores containing some nitrogen in the fully aggregated form (B centres) and yellow outer layers containing C centres, occur at both localities. Carbon isotope compositions and N contents also are significantly different in such core and rim zones, documenting growth during at least two temporally distinct events and involving different diamond forming fluids. Based on their nitrogen characteristics, both the yellow diamonds and yellow rims must have crystallized in close temporal proximity (<<1 Ma) to kimberlite activity at CH-7 and Misery.
Mineralogy and Petrology, in press available 13p. Pdf
Canada, Northwest Territories
deposit - Chidliak, Ekati
Abstract: Yellow diamonds from the CH-7 (Chidliak) and the Misery (Ekati Mine) kimberlites in northern Canada are characterised for their nitrogen characteristics, visible light absorption, internal growth textures, and carbon isotope compositions. The diamonds are generally nitrogen-rich, with median N contents of 1230 (CH-7) and 1030 at.ppm (Misery). Normally a rare feature in natural diamonds, single substitutional nitrogen (C centres) and related features are detected in infrared absorption spectra of 64% of the studied diamonds from CH-7 and 87% from Misery and are considered as the major factor responsible for their yellow colouration. Episodically grown diamonds, characterised by colourless cores containing some nitrogen in the fully aggregated form (B centres) and yellow outer layers containing C centres, occur at both localities. Carbon isotope compositions and N contents also are significantly different in such core and rim zones, documenting growth during at least two temporally distinct events and involving different diamond forming fluids. Based on their nitrogen characteristics, both the yellow diamonds and yellow rims must have crystallized in close temporal proximity (<<1 Ma) to kimberlite activity at CH-7 and Misery.
International Journal of Mining and Geo-Engineering, 11p. Pdf
India
deposit - Wajrakarur
Abstract: A plausible case of collective and economical mining of diamondiferous kimberlite deposits of Wajrakarur and adjoining places in Andhra Pradesh, southern India along with the whole-rock geochemical evidences in support of their diamond potentiality are discussed in this article. The kimberlites/lamproites are mantle-derived ultrabasic rocks which rarely carry diamonds from mantle to the earth’s surface through carrot-shaped intrusions referred to as pipes. Even though few hundreds of diamondiferous kimberlite pipes were discovered in India so far, there is no other production unit than Panna diamond mine in the country where primary rock is mined. In ancient India, diamond mining in south India in the Krishna river valley was well-known to the world fascinated by famous gemstones like Koh-I-Noor, Hope, Darya-e-Noor, Noor-ul-ain etc. which were mainly extracted from alluvium or colluvium in Krishna river valley. Having bestowed with more than 45 kimberlite pipes, the Wajrakarur kimberlite field (WKF) forms a favourable region for initiating diamond mining in the country. Geochemically, majority of the WKF show low TiO2 content and considerably high diamond grade (DG) values (>3) except some pipes viz., P-5 (Muligiripalli), P-13 (Tummatapalli) and P-16 (Pennahobilam) are barren due to high TiO2 and ilmenite contents. The TiO2 content (0.66-6.62 wt%) is inversely proportional to the DG (3.33 to 22.13). The DG value of some of the WKF pipes is close to that of Panna (8.36). The cationic weight% values clearly portray the diamondiferous nature of these deposits. The WKF pipes were also proved to be diamondiferous by exploratory drilling and bulk sample processing results by the government organisations. In southern India, due to several reasons, diamond mining has not seen its initiation and impetus till now although it records a considerable number of fertile kimberlite pipes at Wajrakarur, Lattavaram, Chigicherla, Timmasamudram etc. Though the majority of WKF diamondiferous kimberlite deposits in Wajrakarur are small in their areal extent (0.06-4.48 Ha) some of them are large (>10 Ha up to 120 ha). They occur in close proximity to each other offering feasibility for collective mining and winning the precious stone through a central processing unit by deploying the latest processing technologies. The geographic conditions of this region such as availability of human resources, water resources, vast open lands, wind power generation etc. also support to initiate mining of kimberlite pipes in this area. The availability of rough diamonds produced from local mines will make the polishing industry to meet its business needs during circumstances of the shortage of rough stone influx from foreign. Hence, although it demands liberal investments, reviving diamond mining in southern India can be materialised with a meticulous evaluation of these deposits ascertaining profitability. This will certainly help to restore the past glory of diamond mining in the southern part of the subcontinent.
Abstract: Kimberlites are mantle-derived magmas that either crystallise as hypabyssal intrusions, erupt explosively after rapid ascent to the surface, or less commonly form lava lakes and flows, thereby creating texturally distinct kimberlite units. Efforts to fully understand the processes responsible for the explosive eruption of kimberlite magmas have been hindered by the widespread alteration and crustal contamination of most volcaniclastic kimberlites. To address this issue, we have undertaken a detailed petrographic and mineral chemical study of fresh (i.e. minimally altered) pyroclastic and hypabyssal kimberlites (HK) from the ca. 55-56?Ma A154 North and South kimberlite pipes in the Diavik Mine (Lac de Gras, Canada). These localities host exceptionally fresh kimberlites and are therefore ideally suited to this study. Kimberlite emplacement at A154 North and South initiated with the intrusion of hypabyssal kimberlite (external dykes), and was followed by the explosive formation of kimberlite pipes and volcaniclastic kimberlite infill. Subsequent kimberlite magmas intruded the volcaniclastic kimberlite units forming multiple cross-cutting, internal dykes. The studied volcaniclastic units feature abundant rounded magmaclasts and massive textures, suggestive of primary deposits. These units are classified as pyroclastic kimberlites (PK). Pyroclastic and hypabyssal kimberlite units at Diavik exhibit subtle mineral compositional differences. Samples from both internal HK units and PK units feature identical compositions for liquidus olivine rims (Mg#?=?90.5?±?0.1 and 90.7?±?0.2, respectively), with a marginally lower Mg# of 90.2?±?0.2 in olivine rims from the external HK dykes. Similarly, early-formed chromite compositions are the same for internal HK and PK units (Cr#?=?79.1?±?3.4 and 78.3?±?5.7; Mg#?=?60.0?±?1.3 and 60.0?±?2.2), but, differ in the external HK units (Cr#?=?86.9?±?2.7; Mg#?=?52.8?±?1.9). The internal HK and PK units also exhibit lower carbonate contents than the internal HK units. These compositional differences indicate that the external dykes were probably derived from slightly different primitive melt compositions to those parental to the internal HK and PK units. Spinel evolutionary trends from chromite to magnesian ulv?spinel-magnetite (MUM) compositions (Fe3+#?=?47.2?±?5.8 and 49.7?±?9.3; Cr#?=?25.7?±?11.0 and 17.0?±?14.0 for MUM) are indistinguishable in internal HK and PK samples. These results demonstrate that the primitive melt compositions and early magmatic evolution processes are identical for the internal kimberlite units, regardless of whether the kimberlite melts erupted explosively or were emplaced as shallow intrusions. However, magmaclasts in the PK units contain higher abundances of phlogopite (<52 vol%) and lower quantities of carbonate (<4 vol%) than the groundmass of the hypabyssal kimberlite samples (<2 vol% and 25-65 vol%, respectively). This indicates that the explosively erupted magmas featured higher H2O/CO2 ratios. In contrast, abundant carbonates, including dolomite, in the internal HK samples indicate that CO2, and therefore low H2O/CO2 ratios, were retained during the emplacement of this magma, which likely prevented phlogopite crystallisation. Lower K and Rb whole-rock compositions for internal HK samples compared to PK samples, are attributed to the removal of these components in late-stage kimberlitic fluids, as indicated by hydrothermal alteration of the adjacent volcaniclastic kimberlite units. The above results clearly rule out variations in primitive melt composition and melt evolution trajectories as a primary control on the explosive behaviour of the kimberlite magmas at Diavik. Our study also emphasises how volatile loss resulting from different emplacement styles can have a profound effect on the whole-rock compositions and petrography of kimberlite units. Controls on kimberlite explosivity at Diavik are likely due to external factors, such as local stress regimes, the availability of groundwater (i.e. phreatomagmatism) and differing magma supply rates.
Abstract: Lower crustal heat production is poorly constrained due to the relative inaccessibility of lower crustal samples and their inherent complexity. To obtain the requisite information, the current project conducts spatially resolved geochemical analyses on minerals in 15 lower crustal xenoliths erupted via the Diavik A-154 kimberlite of the Northwest Territories, Canada. The aims are to: 1) conduct geothermometric measurements on lower crustal minerals, 2) construct a heatproducing element budget of the lower crust of the Slave craton, and 3) test the validity of these measurements in a parameter space relevant to geodynamic modeling and diamond exploration. The Diavik lower crustal xenolith suite comprises two main lithologies, mafic granulite (garnet-plagioclase-clinopyroxene ± orthopyroxene) and metasedimentary granulite (garnetplagioclase- orthopyroxene ± quartz ± K-feldspar ± kyanite), which are present in proportions of approximately 80:20, respectively. Application of mineral-pair, iron-magnesium exchange geothermometers (garnet-biotite, garnet-amphibole, and garnet-clinopyroxene) to these xenoliths indicates that the lower crust was at a maximum temperature of roughly 500 °C at the time of kimberlite eruption (~ 55 Ma). The actual temperature of the lower crust is likely lower than 500 °C as the geothermometers probably record the closure temperature of diffusional Fe2+-Mg exchange between touching mineral pairs rather than the ambient temperature of the rocks prior to their entrainment in the kimberlite magma. Heat-producing element (HPE) concentration measurements show that the lower crustal heat production of the Slave craton is likely 0.14 ± 0.02 ?W/m3, which is lower than most values in the literature but broadly comparable to some geophysical estimates. This estimate is the result of (20:80) bimodal mixing of idealized lower crustal endmembers: a metasedimentary lower crust (0.37 ± 0.06 ?W/m3) and a mafic lower crust (0.08 ± 0.01 ?W/m3). These endmembers were iii calculated via a reconstructed bulk rock calculation utilizing trace element concentrations of constituent lower crustal minerals and idealized lithologies from the lower crustal xenoliths. Using these heat production estimates and other crustal parameters such as continental heat flux, mantle heat flux, crustal thickness, and crustal thermal conductivity, I modeled a Moho temperature for the Slave craton of 425 °C, which is consistent with maximum lower crustal temperature estimate given by geothermometry. Adjusting the lower crustal heat production in the geotherm modeling program FITPLOT changes the temperature of the Moho in a similar fashion to the calculated models; however, the diamond propensity of the mantle lithosphere (partially a function of Moho temperature and heat production) does not appear to be strongly affected by a changing Moho temperature and is more strongly controlled by the conditions of the mantle P-T array.
Abstract: Diamondiferous rock types worldwide are broadly divided into kimberlite and lamproite, the latter of which have unique characteristics in different regions and include carbonate-rich varieties (formerly orangeites/Group II kimberlites). Diamondiferous rocks in West Africa are typically micaceous and share petrographic, mineralogical, and geochemical characteristics with both kimberlites and lamproites. To further constrain the classification and petrogenesis of diamondiferous rocks worldwide and their variability between different cratonic regions, in this study we combine detailed petrographic observations with olivine, phlogopite, and spinel chemistry for hypabyssal samples from the Jurassic Tongo dike (Sierra Leone) and the Neoproterozoic Weasua cluster (Liberia). The Tongo dike contains macrocrysts of olivine and phlogopite in a groundmass of olivine, abundant phlogopite, spinel, perovskite, and apatite with a base of calcite, dolomite, and lesser serpentine. The phlogopite is characterised by concurrent FeO and Al2O3 enrichment, which is typical of kimberlites and unlike lamproites. These features and the kimberlite-like spinel compositions allow us to classify the Tongo samples as micaceous kimberlites. The Weasua rocks comprise macrocrysts of olivine in a groundmass of olivine, phlogopite, diopside (zoned towards aegirine-rich rims), spinel, perovskite, and apatite with a base of serpentine and less common calcite. The composition of Weasua phlogopite trends to significant FeO enrichment and Al2O3 depletion, i.e. towards tetraferriphlogopite. The enrichment in mica, phlogopite chemistry and presence of magmatic diopside indicates that these rocks are olivine lamproites. The populations of olivine macrocrysts and microcrysts at Tongo and Weasua are similar and characterised by distinct core and rim zones. Two distinct olivine core populations are observed. 1) forsterite-rich (Fo?>?90) olivine interpreted to reflect xenocrysts from typical mantle peridotites. Al-in-olivine thermometry suggests that these cores have P-T equilibration within diamond stability at Weasua and Tongo. 2) Al-, Ca- and Na- rich cores with P-T formation conditions extending beyond the mantle adiabat. These cores are interpreted to reflect metasomatic and thermal perturbation linked with the infiltration of kimberlite/lamproite melts in the deep lithosphere shortly before entrainment in the ascending magma. The olivine rims at Tongo and Weasua show limited variations in Fo contents at similar values of 88.9?±?0.8 for Tongo and 89.6?±?1.2 for Weasua, as well as similar minor and trace element concentrations. Thus, whereas the Tongo and Weasua rock types are classified as kimberlite and olivine lamproite, respectively, the olivine chemistry suggests a similar petrogenetic evolution.
Abstract: By virtue of their exceptionally deep origin and unique geological histories, diamonds have been found to contain a variety of minerals that are otherwise rare or absent at Earth’s surface. During examination of a type IIa diamond sample from the Letseng mine, Lesotho, a new nickel sulfide mineral was found as part of a fine-grained multiphase inclusion. This nickel sulfide is the natural analogue of the synthetic nickel monosulfide known as ?-NiS, with a NiAs-type structure. This new mineral has been named crowningshieldite, after G.R. Crowningshield (1919 - 2006), whose many years of innovation at the Gemological Institute of America produced countless advances in the understanding and identification of natural, treated and synthetic diamonds and other gem materials. Crowningshieldite is the high-temperature polymorph of millerite, with an inversion temperature of 379 °C from previous experiments on pure NiS. The observed sample of crowningshieldite has an empirical formula of (Ni0.90Fe0.10)S. The host diamond is gemmy, colorless, and relatively pure (type IIa, containing less than ~5 ppm nitrogen). It belongs to a variety of sublithospheric/superdeep diamonds named CLIPPIR diamonds that are notable for their metallic Fe-Ni-C-S melt inclusions. In this case, the inclusion is interpreted to be an alteration assemblage produced when a primary metallic Fe-Ni-C-S inclusion with a surface-reaching fracture reacted with hot fluids, likely associated with kimberlite emplacement. Other phases identified in association with crowningshieldite in this fine-grained alteration assemblage are magnetite-magnesioferrite, hematite, and graphite. Unexposed inclusions within the same diamond are of original, unaltered Fe-Ni-C-S composition. The new mineral crowningshieldite is a good example of the complexity and breadth of geological processes recorded within diamonds and their inclusions.
