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SDLRC - Scientific Articles all years by Author - Gi-Gq
The Sheahan Diamond Literature Reference Compilation
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 announcementscalled 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 Resource Center
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
The SDLRC provides 3 types of references identified in the reference code. DS for scientific article, DM for a media article, and DC for a corporate announcement. Consider DS0512-0001. The DS stands for "diamond scientific". 05 stands for 2005, the year the reference was posted. 12 represents the month the reference was posted. For all years prior to 2015 the default month is 12. -0001 is the reference's identifier and it does not mean anything. The number below the refence code, ie 2015, is the year the article was published. Note that the posted year may sometimes be later than the published year.
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Dr. D. Twitchen ( CVD Element Six) discussion using magnetic resonance and optical techniques to study how defects in diamond affect colour and electrical conductivity. Keynote speaker
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 Bańos 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.
Abstract: Super-deep diamonds (SDDs) are those that form at depths between ~300 and ~1000 km in Earth’s mantle. They compose only 1% of the entire diamond population but play a pivotal role in geology, as they represent the deepest direct samples from the interior of our planet. Ferropericlase, (Mg,Fe)O, is the most abundant mineral found as inclusions in SDDs and, when associated with low-Ni enstatite, which is interpreted as retrogressed bridgmanite, is considered proof of a lower-mantle origin. As this mineral association in diamond is very rare, the depth of formation of most ferropericlase inclusions remains uncertain. Here we report geobarometric estimates based on both elasticity and elastoplasticity theories for two ferropericlase inclusions, not associated with enstatite, from a single Brazilian diamond. We obtained a minimum depth of entrapment of 15.7 (±2.5) GPa at 1830 (±45) K (~450 [±70] km depth), placing the origin of the diamond-inclusion pairs at least near the upper mantle-transition zone boundary and confirming their super-deep origin. Our analytical approach can be applied to any type of mineral inclusion in diamond and is expected to allow better insights into the depth distribution and origin of SDDs.
Earth and Planetary Science Letters, Vol. 451, pp. 114-124.
Mantle
Subduction
Abstract: The elastic properties of two single crystals of majoritic garnet (Mg3.24Al1.53Si3.23O12 and Mg3.01Fe0.17Al1.68Si3.15O12), have been measured using simultaneously single-crystal X-ray diffraction and Brillouin spectroscopy in an externally heated diamond anvil cell with Ne as pressure transmitting medium at conditions up to ~30 GPa and ~600 K. This combination of techniques makes it possible to use the bulk modulus and unit-cell volume at each condition to calculate the absolute pressure, independently of secondary pressure calibrants. Substitution of the majorite component into pyrope garnet lowers both the bulk (KsKs) and shear modulus (G ). The substitution of Fe was found to cause a small but resolvable increase in KsKs that was accompanied by a decrease in ?Ks/?P?Ks/?P, the first pressure derivative of the bulk modulus. Fe substitution had no influence on either the shear modulus or its pressure derivative. The obtained elasticity data were used to derive a thermo-elastic model to describe VsVs and VpVp of complex garnet solid solutions. Using further elasticity data from the literature and thermodynamic models for mantle phase relations, velocities for mafic, harzburgitic and lherzolitic bulk compositions at the base of Earth's transition zone were calculated. The results show that VsVs predicted by seismic reference models are faster than those calculated for all three types of lithologies along a typical mantle adiabat within the bottom 150 km of the transition zone. The anomalously fast seismic shear velocities might be explained if laterally extensive sections of subducted harzburgite-rich slabs pile up at the base of the transition zone and lower average mantle temperatures within this depth range.
Abstract: We report on pipe-like bodies and dikes of carbonate rocks related to sodic alkaline intrusions and amphibole mantle peridotites in the Ivrea zone (European Southern Alps). The carbonate rocks have bulk trace-element concentrations typical of low-rare earth element carbonatites interpreted as cumulates of carbonatite melts. Faintly zoned zircons from these carbonate rocks contain calcite inclusions and have trace-element compositions akin to those of carbonatite zircons. Laser ablation-inductively coupled plasma-mass spectrometry U-Pb zircon dating yields concordant ages of 187 ± 2.4 and 192 ± 2.5 Ma, coeval with sodic alkaline magmatism in the Ivrea zone. Cross-cutting relations, ages, as well as bulk and zircon geochemistry indicate that the carbonate rocks are carbonatites, the first ones reported from the Alps. Carbonatites and alkaline intrusions are comagmatic and were emplaced in the nascent passive margin of Adria during the Early Jurassic breakup of Pangea. Extension caused partial melting of amphibole-rich mantle domains, yielding sodic alkaline magmas whose fractionation led to carbonatite-silicate melt immiscibility. Similar occurrences in other rifts suggest that small-scale, sodic and CO2-rich alkaline magmatism is a typical result of extension and decompression-driven reactivation of amphibole-bearing lithospheric mantle during passive continental breakup and the evolution of magma-poor rifts.
Earth and Planetary Science Letters, Vol. 539, 116240 9p. Pdf
Mantle
geophysics - seismics
Abstract: Earth's thermo-chemical structure exerts a fundamental control on mantle convection, plate tectonics, and surface volcanism. There are indications that mantle convection occurs as an intermittent-stage process between layered and whole mantle convection in interaction with a compositional stratification at 660 km depth. However, the presence and possible role of any compositional layering in the mantle remains to be ascertained and understood. By interfacing inversion of a novel global seismic data set with petrologic phase equilibrium calculations, we show that a compositional boundary is not required to explain short- and long-period seismic data sensitive to the upper mantle and transition zone beneath stable continental regions; yet, radial enrichment in basaltic material reproduces part of the complexity present in the data recorded near subduction zones and volcanically active regions. Our findings further indicate that: 1) cratonic regions are characterized by low mantle potential temperatures and significant lateral variability in mantle composition; and 2) chemical equilibration seems more difficult to achieve beneath stable cratonic regions. These findings suggest that the lithologic integrity of the subducted basalt and harzburgite may be better preserved for geologically significant times underneath cratonic regions.
The aeromagnetic survey program of the Geological Society of Canada (GSC)- implications for kimberliteexploration.
Mid-continent diamonds Geological Association of Canada (GAC)-Mineralogical Association of Canada (MAC) Symposium ABSTRACT volume, held Edmonton May, pp. 27-30.
Abstract: A "happy accident" has yielded a new, stable form of pure carbon made from cheap feedstocks, researchers say. Like diamond and graphene, two other guises of carbon, the material seems to have extraordinary physical properties. It is harder than stainless steel, about as conductive, and as reflective as a polished aluminum mirror. Perhaps most surprising, the substance appears to be ferromagnetic, behaving like a permanent magnet at temperatures up to 125°C. The discovery, announced in a talk here at the International Symposium on Clusters and Nanomaterials, could lead to lightweight coatings, medical products, and novel electronic devices. The news has elicited both excitement and caution among the dozens of researchers attending the meeting. Experts note that carbon is much lighter than other ferromagnetic elements such as manganese, nickel, and iron. Moreover, carbon is nontoxic in the body—which could mean the substance could be used for making biosensors or drug-delivery carriers.
Contents of trace elements in olivines from diamonds and peridotite xenoliths of the V.Grib kimberlite pipe ( Arkhangel'sk Diamondiferous province, Russia).
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: 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.
Abstract: According to present views, the crustal terranes of the Anabar province of the Siberian craton were initially independent blocks, separated from the convecting mantle at 3.1 (Daldyn terrane), 2.9 (Magan terrane) and 2.5?Ga (Markha terrane) (Rosen, 2003, 2004; Rosen et al., 1994, 2005, 2009). Previous studies of zircons in a suite of crustal xenoliths from kimberlite pipes of the Markha terrane concluded that the evolution of the crust of the Markha terrane is very similar to that of the Daldyn terrane. To test this conclusion we present results of U-Pb and Hf-isotope studies on zircons in crustal xenoliths from the Zapolyarnaya kimberlite pipe (Upper Muna kimberlite field), located within the Daldyn terrane, and the Botuobinskaya pipe (Nakyn kimberlite field) in the center of the Markha terrane. The data on xenoliths from the Botuobinskaya kimberlite pipe record tectonothermal events at 2.94, 2.8, 2.7 and 2?Ga. The event at 2?Ga caused Pb loss in zircons from a mafic granulite. U-Pb dating of zircons from the Zapolyarnaya pipe gives an age of 2.7?Ga. All zircons from the studied crustal xenoliths have Archean Hf model ages ranging from 3.65 to 3.11?Ga. This relatively narrow range suggests that reworking of the ancient crust beneath the Nakyn and Upper Muna kimberlite fields was minor, compared with the Daldyn and Alakit-Markha fields (Shatsky et al., 2016). This study, when combined with dating of detrital zircons, implies that tectonic-thermal events at 2.9-2.85, 2.75-2.7 and 2.0-1.95?Ga occurred everywhere on the Anabar tectonic province, and could reflect the upwelling of superplumes at 2.9, 2.7 and 2?Ga. The presence of the same tectonic-thermal events in the Daldyn and Markha terranes (Rosen et al., 2006a,b) supports the conclusion that the identification of the Markha terrane as a separate unit is not valid.
Abstract: According to present views, the crustal terranes of the Anabar province of the Siberian craton were initially independent blocks, separated from the convecting mantle at 3.1 (Daldyn terrane), 2.9 (Magan terrane) and 2.5?Ga (Markha terrane) (Rosen, 2003, 2004; Rosen et al., 1994, 2005, 2009). Previous studies of zircons in a suite of crustal xenoliths from kimberlite pipes of the Markha terrane concluded that the evolution of the crust of the Markha terrane is very similar to that of the Daldyn terrane. To test this conclusion we present results of U-Pb and Hf-isotope studies on zircons in crustal xenoliths from the Zapolyarnaya kimberlite pipe (Upper Muna kimberlite field), located within the Daldyn terrane, and the Botuobinskaya pipe (Nakyn kimberlite field) in the center of the Markha terrane. The data on xenoliths from the Botuobinskaya kimberlite pipe record tectonothermal events at 2.94, 2.8, 2.7 and 2?Ga. The event at 2?Ga caused Pb loss in zircons from a mafic granulite. U-Pb dating of zircons from the Zapolyarnaya pipe gives an age of 2.7?Ga. All zircons from the studied crustal xenoliths have Archean Hf model ages ranging from 3.65 to 3.11?Ga. This relatively narrow range suggests that reworking of the ancient crust beneath the Nakyn and Upper Muna kimberlite fields was minor, compared with the Daldyn and Alakit-Markha fields (Shatsky et al., 2016). This study, when combined with dating of detrital zircons, implies that tectonic-thermal events at 2.9 -2.85, 2.75 -2.7 and 2.0 -1.95?Ga occurred everywhere on the Anabar tectonic province, and could reflect the upwelling of superplumes at 2.9, 2.7 and 2?Ga. The presence of the same tectonic-thermal events in the Daldyn and Markha terranes (Rosen et al., 2006a,b) supports the conclusion that the identification of the Markha terrane as a separate unit is not valid.
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: To gain better insight into the thermal state and composition of the lithospheric mantle beneath the Upper Muna kimberlite field (Siberian craton), a suite of 323 clinopyroxene xenocrysts and 10 mantle xenoliths from the Komsomolskaya-Magnitnaya (KM) pipe have been studied. We selected 188 clinopyroxene grains suitable for precise pressure (P)-temperature (T) estimation using single-clinopyroxene thermobarometry. The majority of P-T points lie along a narrow, elongated field in P-T space with a cluster of high-T and high-P points above 1300 °C, which deviates from the main P-T trend. The latter points may record a thermal event associated with kimberlite magmatism (a “stepped” or “kinked” geotherm). In order to eliminate these factors, the steady-state mantle paleogeotherm for the KM pipe at the time of initiation of kimberlite magmatism (Late Devonian-Early Carboniferous) was constrained by numerical fitting of P-T points below T = 1200 °C. The obtained mantle paleogeotherm is similar to the one from the nearby Novinka pipe, corresponding to a ~34-35 mW/m2 surface heat flux, 225-230 km lithospheric thickness, and 110-120 thick "diamond window" for the Upper Muna field. Coarse peridotite xenoliths are consistent in their P-T estimates with the steady-state mantle paleogeotherm derived from clinopyroxene xenocrysts, whereas porphyroclastic ones plot within the cluster of high-T and high-P clinopyroxene xenocrysts. Discrimination using Cr2O3 demonstrates that peridotitic clinopyroxene xenocrysts are prevalent (89%) among all studied 323 xenocrysts, suggesting that the Upper Muna mantle is predominantly composed of peridotites. Clinopyroxene-poor or -free peridotitic rocks such as harzburgites and dunites may be evident at depths of 140-180 km in the Upper Muna mantle. Judging solely from the thermal considerations and the thickness of the lithosphere, the KM and Novinka pipes should have excellent diamond potential. However, all pipes in the Upper Muna field have low diamond grades (<0.9, in carats/ton), although the lithosphere thickness is almost similar to the values obtained for the high-grade Udachnaya and Mir pipes from the Daldyn and Mirny fields, respectively. Therefore, other factors have affected the diamond grade of the Upper Muna kimberlite field.
Abstract: The permafrost zone is expected to be a substantial carbon source to the atmosphere, yet large-scale models currently only simulate gradual changes in seasonally thawed soil. Abrupt thaw will probably occur in <20% of the permafrost zone but could affect half of permafrost carbon through collapsing ground, rapid erosion and landslides. Here, we synthesize the best available information and develop inventory models to simulate abrupt thaw impacts on permafrost carbon balance. Emissions across 2.5?million?km2 of abrupt thaw could provide a similar climate feedback as gradual thaw emissions from the entire 18?million?km2 permafrost region under the warming projection of Representative Concentration Pathway 8.5. While models forecast that gradual thaw may lead to net ecosystem carbon uptake under projections of Representative Concentration Pathway 4.5, abrupt thaw emissions are likely to offset this potential carbon sink. Active hillslope erosional features will occupy 3% of abrupt thaw terrain by 2300 but emit one-third of abrupt thaw carbon losses. Thaw lakes and wetlands are methane hot spots but their carbon release is partially offset by slowly regrowing vegetation. After considering abrupt thaw stabilization, lake drainage and soil carbon uptake by vegetation regrowth, we conclude that models considering only gradual permafrost thaw are substantially underestimating carbon emissions from thawing permafrost.
An overview of Triassic stratigraphy and depositional environments in the Rocky Mountain foothills and western interior plains, Peace River Arch region
Geology of the Peace River Arch, ed. Sc.C. O'Connell, J.S. Bell, Bulletin. Can., Vol. 38A, Special Volume, December pp. 146-158
Abstract: Evidence for chemical and lithological heterogeneity in the Earth’s convecting mantle is widely acknowledged, yet the major element signature imparted on mantle melts by this heterogeneity is still poorly resolved. In this study, a recent thermodynamic melting model is tested on a range of compositions that correspond to potential mantle lithologies (harzburgitic to pyroxenitic), to demonstrate its applicability over this compositional range, in particular for pyroxenite melting. Our results show that, despite the model’s calibration in peridotitic systems, it effectively reproduces experimental partial melt compositions for both Si-deficient and Si-excess pyroxenites. Importantly, the model accurately predicts the presence of a free silica phase at high pressures in Si-excess pyroxenites, indicating the activation of the pyroxene-garnet thermal divide. This thermal divide has a dominant control on solidus temperature, melt productivity and partial melt composition. The model is used to make new inferences on the link between mantle composition and melting behaviour. In silica-deficient and low-pressure (olivine-bearing) lithologies, melt composition is not very sensitive to source composition. Linearly varying the source composition between peridotite and basaltic pyroxenite, we find that the concentration of oxides in the melt tends to be buffered by the increased stability of more fusible phases, causing partial melts of even highly fertile lithologies to be similar to those of peridotite. An exception to this behaviour is FeO, which is elevated in partial melts of silica-deficient pyroxenite even if the bulk composition does not have a high FeO content relative to peridotite. Melt Al2O3 and MgO vary predominantly as a function of melting depth rather than bulk composition. We have applied the thermodynamic model to test the hypothesis that Fe-rich mantle melts such as ferropicrites are derived by partial melting of Si-deficient pyroxenite at elevated mantle potential temperatures. We show that the conspicuously high FeO in ferropicrites at a given MgO content does not require a high-Fe mantle source and is indeed best matched by model results involving around 0-20% melting of silica-deficient pyroxenite. A pyroxenite source lithology also accounts for the low CaO content of ferropicrites, whereas their characteristic low Al2O3 is a function of their high pressure of formation. Phanerozoic ferropicrites are exclusively located in continental flood basalt (CFB) provinces and this model of formation confirms that lithological heterogeneity (perhaps recycled oceanic crust) is present in CFB mantle sources.
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.
Overt and cryptic strongly potassic mafic liquids in the Neogene magmatism of the n.part of the Rio Grande Rift, USA: a lithospheric drip feed into asthenospheric so
Proceedings of Fifth International Kimberlite Conference held Araxa June 1991, Servico Geologico do Brasil (CPRM) Special, pp. 420-422
Timescales and mechanisms of plume-lithosphere interactions: Ar/Ar geochronology and geochemistry of alkaline igneous rocks from the Parana Etendeka igneous
Earth and Planetary Science Letters, Vol. 251, 1-2, Nov. 15, pp. 1-17.
Multiple reaction oxygen barometry for mantle peridotite: an internally consistent thermodynamic model for reactions and garnet solid-solutions, with applications to the oxidation state of lithospheric mantle.
Volcanic and Magmatic Studies Group meeting, Poster Held Jan. 6-8. See minsoc website
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.
Abstract: New thermodynamic data for skiagite garnet (Fe3Fe23+Si3O12) are derived from experimental phase-equilibrium data that extend to 10 GPa and are applied to oxybarometry of mantle peridotites using a revised six-component garnet mixing model. Skiagite is more stable by 12 kJ mol-1 than in a previous calibration of the equilibrium 2 skiagite = 4 fayalite + ferrosilite + O2, and this leads to calculated oxygen fugacities that are higher (more oxidized) by around 1-1•5 logfO2 units. A new calculation method and computer program incorporates four independent oxybarometers (including 2 pyrope + 2 andradite + 2 ferrosilite = 2 grossular + 4 fayalite + 3 enstatite + O2) for use on natural peridotite samples to yield optimum logfO2 estimates by the method of least squares. These estimates should be more robust than those based on any single barometer and allow assessment of possible disequilibrium in assemblages. A new set of independent oxybarometers for spinel-bearing peridotites is also presented here, including a new reaction 2 magnetite + 3 enstatite = 3 fayalite + 3 forsterite + O2. These recalibrations combined with internally consistent PT determinations for published analyses of mantle peridotites with analysed Fe2O3 data for garnets, from both cratonic (Kaapvaal, Siberia and Slave) and circumcratonic (Baikal Rift) regions, provide revised estimates of oxidation state in the lithospheric mantle. Estimates of logfO2 for spinel assemblages are more reduced than those based on earlier calibrations, whereas garnet-bearing assemblages are more oxidized. Importantly, this lessens considerably the difference between garnet and spinel oxybarometry that was observed with previous published calibrations.
Geochimica et Cosmochimica Acta, in press available
Africa, Namibia
Picrite, ferroPicrite
Abstract: We present major and trace element compositions of 154 re-homogenised olivine-hosted melt inclusions found in primitive rocks (picrites and ferropicrites) from the Mesozoic Paraná-Etendeka and Karoo Continental Flood Basalt (CFB) provinces. The major element compositions of the melt inclusions, especially their Fe/Mg ratios, are variable and erratic, and attributed to the re-homogenisation process during sample preparation. In contrast, the trace element compositions of both the picrite and ferropicrite olivine-hosted melt inclusions are remarkably uniform and closely reflect those of the host whole-rocks, except in a small subset affected by hydrothermal alteration. The Paraná-Etendeka picrites and ferropicrites are petrogenetically related to the more evolved and voluminous flood basalts, and so we propose that compositional homogeneity at the melt inclusion scale implies that the CFB parental mantle melts were well mixed prior to extensive crystallisation. The incompatible trace element homogeneity of olivine-hosted melt inclusions in Paraná-Etendeka and Karoo near primitive magmatic rocks has also been identified in other CFB provinces and contrasts with findings from studies of basalts from mid-ocean ridges (e.g. Iceland and FAMOUS on the Mid Atlantic Ridge), where heterogeneity of incompatible trace elements in olivine-hosted melt inclusions is much more pronounced. We suggest that the low variability in incompatible trace element contents of olivine-hosted melt inclusions in near-primitive CFB rocks, and also ocean island basalts associated with moderately thick lithosphere (e.g. Hawaii, Galápagos, Samoa) may reflect mixing along their longer transport pathways during ascent and/or a temperature contrast between the liquidus and the liquid when it arrives in the crust. These thermal paths promote mixing of mantle melts prior to their entrapment by growing olivine crystals in crustal magma chambers. Olivine-hosted melt inclusions of ferropicrites from the Paraná-Etendeka and Karoo CFB have the least variable compositions of all global melt inclusion suites, which may be a function of their unusually deep origin and low viscosity.
Geochimica et Cosmochimica Acta, Vol. 196, pp. 36-57.
Africa, Namibia, Angola
Paran-Etendeka, Karoo
Abstract: We present major and trace element compositions of 154 re-homogenised olivine-hosted melt inclusions found in primitive rocks (picrites and ferropicrites) from the Mesozoic Parana ´-Etendeka and Karoo Continental Flood Basalt (CFB) provinces. The major element compositions of the melt inclusions, especially their Fe/Mg ratios, are variable and erratic, and attributed to the re-homogenisation process during sample preparation. In contrast, the trace element compositions of both the picrite and ferropicrite olivine-hosted melt inclusions are remarkably uniform and closely re?ect those of the host whole-rocks, except in a small subset a?ected by hydrothermal alteration. The Parana ´-Etendeka picrites and ferropicrites are petrogenet- ically related to the more evolved and voluminous ?ood basalts, and so we propose that compositional homogeneity at the melt inclusion scale implies that the CFB parental mantle melts were well mixed prior to extensive crystallisation. The incompatible trace element homogeneity of olivine-hosted melt inclusions in Parana ´-Etendeka and Karoo primitive magmatic rocks has also been identi?ed in other CFB provinces and contrasts with ?ndings from studies of basalts from mid- ocean ridges (e.g. Iceland and FAMOUS on the Mid Atlantic Ridge), where heterogeneity of incompatible trace elements in olivine-hosted melt inclusions is more pronounced. We suggest that the low variability in incompatible trace element contents of olivine-hosted melt inclusions in near-primitive CFB rocks, and also ocean island basalts associated with moderately thick lithosphere (e.g. Hawaii, Gala ´pagos, Samoa), may re?ect mixing along their longer transport pathways during ascent and/or a temperature contrast between the liquidus and the liquid when it arrives in the crust. These thermal paths promote mixing of mantle melts prior to their entrapment by growing olivine crystals in crustal magma chambers. Olivine-hosted melt inclusions of ferropicrites from the Parana ´-Etendeka and Karoo CFB have the least variable compositions of all global melt inclusion suites, which may be a function of their unusually deep origin and low viscosity.
Abstract: The widespread occurrence of pyrope garnet in Archean lithospheric mantle remains one of the ‘holy grails’ of mantle petrology. Most garnets found in peridotitic mantle equilibrated with incompatible-trace-element-enriched melts or fluids and are the products of metasomatism. Less common are macroscopic intergrowths of pyrope garnet formed by exsolution from orthopyroxene. Spectacular examples of these are preserved in both mantle xenoliths and large, isolated crystals (megacrysts) from the Kaapvaal craton of southern Africa, and provide direct evidence that some garnet in the sub-continental lithospheric mantle initially formed by isochemical rather than metasomatic processes. The orthopyroxene hosts are enstatites and fully equilibrated with their exsolved phases (low-Cr pyrope garnet ±± Cr-diopside). Significantly, P-TP-T estimates of the post-exsolution orthopyroxenes plot along an unperturbed conductive Kaapvaal craton geotherm and reveal that they were entrained from a large continuous depth interval (85 to 175 km). They therefore represent snapshots of processes operating throughout almost the entire thickness of the sub-cratonic lithospheric mantle. New rare-earth element (REE) analyses show that the exsolved garnets occupy the full spectrum recorded by garnets in mantle peridotites and also diamond inclusions. A key finding is that a few low-temperature exsolved garnets, derived from depths of ~90 km, are more depleted in light REEs than previously observed in any other mantle sample. Importantly, the REE patterns of these strongly LREE-depleted garnets resemble the hypothetical composition proposed for pre-metasomatic garnets that are thought to pre-date major enrichment events in the sub-continental lithospheric mantle, including those associated with diamond formation. The recalculated compositions of pre-exsolution orthopyroxenes have higher Al22O33 and CaO contents than their post-exsolution counterparts and most likely formed as shallow residues of large amounts of adiabatic decompression melting in the spinel-stability field. It is inferred that exsolution of garnet from Kaapvaal orthopyroxenes may have been widespread, and perhaps accompanied cratonization at ~ 2.9 to 2.75 Ga. Such a process would considerably increase the density and stability of the continental lithosphere.
Abstract: The widespread occurrence of pyrope garnet in Archean lithospheric mantle remains one of the ‘holy grails’ of mantle petrology. Most garnets found in peridotitic mantle equilibrated with incompatible-trace-element-enriched melts or fluids and are the products of metasomatism. Less common are macroscopic intergrowths of pyrope garnet formed by exsolution from orthopyroxene. Spectacular examples of these are preserved in both mantle xenoliths and large, isolated crystals (megacrysts) from the Kaapvaal craton of southern Africa, and provide direct evidence that some garnet in the sub-continental lithospheric mantle formed initially by isochemical rather than metasomatic processes. The orthopyroxene hosts are enstatites and fully equilibrated with their exsolved phases (low-Cr pyrope garnet?±?Cr-diopside). Significantly, P-T estimates of the post-exsolution orthopyroxenes plot along an unperturbed conductive Kaapvaal craton geotherm and reveal that they were entrained from a large continuous depth interval (85 to 175 km). They therefore represent snapshots of processes operating throughout almost the entire thickness of the sub-cratonic lithospheric mantle. New rare-earth element (REE) analyses show that the exsolved garnets occupy the full spectrum recorded by garnets in mantle peridotites and also diamond inclusions. A key finding is that a few low-temperature exsolved garnets, derived from depths of ~90 km, are more depleted in light rare-earth elements (LREEs) than previously observed in any other mantle sample. Importantly, the REE patterns of these strongly LREE-depleted garnets resemble the hypothetical composition proposed for pre-metasomatic garnets that are thought to pre-date major enrichment events in the sub-continental lithospheric mantle, including those associated with diamond formation. The recalculated compositions of pre-exsolution orthopyroxenes have higher Al2O3 and CaO contents than their post-exsolution counterparts and most probably formed as shallow residues of large amounts of adiabatic decompression melting in the spinel-stability field. It is inferred that exsolution of garnet from Kaapvaal orthopyroxenes may have been widespread, and perhaps accompanied cratonization at ~2.9 to 2.75 Ga. Such a process would considerably increase the density and stability of the continental lithosphere.
Earth and Planetary Science Letters, Vol. 499, pp. 205-218.
Ocean
plumes, hotspots
Abstract: The global mid-ocean ridge (MOR) system represents a major site for outgassing of volatiles from Earth's mantle. The amount of H2O released via eruption of mid-ocean ridge basalts varies along the global ridge system and greatest at sites of interaction with mantle plumes. These deep-sourced thermal anomalies affect approximately one-third of all MORs - as reflected in enrichment of incompatible trace elements, isotope signatures and elevated ridge topography (excess melting) - but the physical mechanisms involved are controversial. The “standard model” involves solid-state flow interaction, wherein an actively upwelling plume influences the divergent upwelling generated by a mid-ocean ridge so that melting occurs at higher pressures and in greater amounts than at a normal spreading ridge. This model does not explain, however, certain enigmatic features including linear volcanic ridges radiating from the active plume to the nearby MOR. Examples of these are the Wolf-Darwin lineament (Galápagos), Rodrigues Ridge (La Réunion), Discovery Ridge (Discovery), and numerous smaller ridge-like structures associated with the Azores and Easter-Salas y Gómez hot spots. An important observation from our study is that fractionation-corrected MORB with exceptionally-high H2O contents (up to 1.3 wt.%) are found in close proximity to intersections of long-lived plume-related volcanic lineaments with spreading centres. New algorithms in the rare-earth element inversion melting (INVMEL) program allow us to simulate plume-ridge interactions by mixing the compositions of volatile-bearing melts generated during both active upwelling and passively-driven corner-flow. Our findings from these empirical models suggest that at sites of plume-ridge interaction, moderately-enriched MORBs (with 0.2-0.4 wt.% H2O) result from mixing of melts formed by: (i) active upwelling of plume material to minimum depths of ~35 km; and (ii) those generated by passive melting at shallower depths beneath the ridge. The most volatile-rich MORB (0.4-1.3 wt.% H2O) may form by the further addition of up to 25% of “deep” small-fraction plume stem melts that contain >3 wt.% H2O. We propose that these volatile-rich melts are transported directly to nearby MOR segments via pressure-induced, highly-channelised flow embedded within a broader “puddle” of mostly solid-state plume material, spreading beneath the plate as a gravity flow. This accounts for the short wavelength variability (over 10s of km) in geochemistry and bathymetry that is superimposed on the much larger (many 100s of km) “waist width” of plume-influenced ridge. Melt channels may constitute a primary delivery mechanism for volatiles from plume stems to nearby MORs and, in some instances, be expressed at the surface as volcanic lineaments and ridges. The delivery of small-fraction hydrous melts from plume stems to ridges via a two-phase (melt-matrix) regime implies that a parallel, bimodal transport system is involved at sites of plume-ridge interaction. We estimate that the rate of emplacement of deep-sourced volatile-rich melts in channels beneath the volcanic lineaments is high and involves 10s of thousands of km3/Ma. Since mantle plumes account for more than half of the melt production at MORs our findings have important implications for our understanding of deep Earth volatile cycling.
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.
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.
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 (eHf (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: Carbon is central to the formation and environmental impact of large igneous provinces (LIPs). These vast magmatic events occur over geologically short timescales and include voluminous flood basalts, along with silicic and low-volume alkaline magmas. Surface outgassing of CO2 from flood basalts may average up to 3,000 Mt per year during LIP emplacement and is subsidized by fractionating magmas deep in the crust. The large quantities of carbon mobilized in LIPs may be sourced from the convecting mantle, lithospheric mantle and crust. The relative significance of each potential carbon source is poorly known and probably varies between LIPs. Because LIPs draw on mantle reservoirs typically untapped during plate boundary magmatism, they are integral to Earth’s long-term carbon cycle.
Geochimica et Cosmochimica Acta, Vol. 275, pp. 140-162.
Mantle
craton
Abstract: The extent to which Earth’s sub-continental lithospheric mantle modulates the flux of volatile elements from our planet’s deep interior to its atmosphere (via volcanism) is poorly constrained. Here, we focus on "off-craton" sub-continental lithospheric mantle because this long-lived reservoir potentially acts as both a volatile “sink” and “source” during major heating and rifting events. The sub-continental lithospheric mantle is primarily formed of peridotites with subordinate amounts of pyroxenites. While both lithologies are dominated by nominally-volatile-free mantle minerals, some of these phases have been shown to contain non-negligible amounts of H2O (e.g. 100’s of ppmw in clinopyroxene). Data for volatile elements other than Li are, however, limited. We present new, high-precision, in-situ Secondary Ion Mass Spectrometry analyses of H, F, Cl, Li and B in olivine and pyroxenes from well-characterised garnet- and spinel-bearing peridotites and pyroxenites (from southern Patagonia and the Antarctic Peninsula). Our study confirms that clinopyroxene is the main host of H2O and F. The maximum F contents we report (up to 154 ppmw) are higher than those in previous studies and occur in Ti-Cr diopsides in highly-metasomatised peridotites and Ti-Al augites from clinopyroxenite veins. Water contents of clinopyroxenes (up to 615 ppmw) are within the range previously published for continental mantle. Lithium concentrations are low (<5 ppmw) in all analysed phases and both Cl and B are below detection levels (14 ppmw and 0.03 ppmw, respectively). Unique to our study is the large variation in major- and trace-element concentrations of the clinopyroxenes, which allows us to place quantitative constraints on how volatiles are stored in the mantle. We demonstrate that: (i) F contents of clinopyroxenes closely correlate with Ti and (ii) and is systematic and inversely correlated with temperature. Despite the redistribution of volatiles during sub-solidus re-equilibration, we show that the first order control on the concentration of volatiles in clinopyroxene is the style of metasomatism, i.e. channellised flow versus reactive percolation. The mean bulk volatile contents of peridotites from Pali Aike and the Antarctic Peninsula (H2O?=?89?±?31 ppmw, F?=?16?±?11.2 ppmw and Li?=?2?±?0.7 ppmw) are within the range previously published for continental "off-craton" mantle. The pyroxenites have significantly higher mean bulk concentrations of H2O (260?±?59 ppmw), F (86?±?43 ppmw) and Li (1.0?±?0.35 ppmw). While the greater capacity of mantle pyroxenites to host H2O relative to the associated peridotites has previously been observed in global "off-craton" mantle xenolith suites (e.g. Oahu, Hawaii; eastern China and the Rio Grande Rift, SW USA), here we show for the first time that pyroxenites are also major hosts of F (but not Cl, Li or B). Because of their relatively low solidus temperatures, pyroxenites in "off-craton" settings will be readily re-mobilised during lithospheric extension (and heating). We suggest these pyroxene-rich mantle lithologies may be responsible for the elevated concentrations of H2O and F observed in basalts and volcanic gasses from major continental rift zones and flood basalt provinces, and hence an important consideration in models of global volatile cycles.
Abstract: The 2060 Ma old Palabora Carbonatite Complex (PCC), South Africa, comprises diverse REE mineral assemblages formed during different stages and reflects an outstanding instance to understand the evolution of a carbonatite-related REE mineralization from orthomagmatic to late-magmatic stages and their secondary post-magmatic overprint. The 10 rare earth element minerals monazite, REE-F-carbonates (bastnäsite, parisite, synchysite), ancylite, britholite, cordylite, fergusonite, REE-Ti-betafite, and anzaite are texturally described and related to the evolutionary stages of the PCC. The identification of the latter five REE minerals during this study represents their first described occurrences in the PCC as well as in a carbonatite complex in South Africa. The variable REE mineral assemblages reflect a multi-stage origin: (1) fergusonite and REE-Ti-betafite occur as inclusions in primary magnetite. Bastnäsite is enclosed in primary calcite and dolomite. These three REE minerals are interpreted as orthomagmatic crystallization products. (2) The most common REE minerals are monazite replacing primary apatite, and britholite texturally related to the serpentinization of forsterite or the replacement of forsterite by chondrodite. Textural relationships suggest that these two REE-minerals precipitated from internally derived late-magmatic to hydrothermal fluids. Their presence seems to be locally controlled by favorable chemical conditions (e.g., presence of precursor minerals that contributed the necessary anions and/or cations for their formation). (3) Late-stage (post-magmatic) REE minerals include ancylite and cordylite replacing primary magmatic REE-Sr-carbonates, anzaite associated with the dissolution of ilmenite, and secondary REE-F-carbonates. The formation of these post-magmatic REE minerals depends on the local availability of a fluid, whose composition is at least partly controlled by the dissolution of primary minerals (e.g., REE-fluorocarbonates). This multi-stage REE mineralization reflects the interplay of magmatic differentiation, destabilization of early magmatic minerals during subsequent evolutionary stages of the carbonatitic system, and late-stage fluid-induced remobilization and re-/precipitation of precursor REE minerals. Based on our findings, the Palabora Carbonatite Complex experienced at least two successive stages of intense fluid–rock interaction.
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: 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.
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.
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.
Abstract: The mineralogy and mineral chemistry of the four major sövite bodies (Badberg, Degenmatt, Haselschacher Buck and Orberg), calcite foidolite/nosean syenite xenoliths (enclosed in the Badberg sövite only) and rare extrusive carbonatites of the Kaiserstuhl Volcanic Complex in Southern Germany provide evidence for contamination processes in the carbonatitic magma system of the Kaiserstuhl. Based on textures and composition, garnet and clinopyroxene in extrusive carbonatites represent xenocrysts entrained from the associated silicate rocks. In contrast, forsterite, monticellite and mica in sövites from Degenmatt, Haselschacher Buck and Orberg probably crystallized from the carbonatitic magma. Clinopyroxene and abundant mica crystallization in the Badberg sövite, however, was induced by the interaction between calcite foidolite xenoliths and the carbonatite melt. Apatite and micas in the various sövite bodies reveal clear compositional differences: apatite from Badberg is higher in REE, Si and Sr than apatite from the other sövite bodies. Mica from Badberg is biotite- and comparatively Fe2+-rich (Mg# = 72-88). Mica from the other sövites, however, is phlogopite (Mg# up to 97), as is typical of carbonatites in general. The typical enrichment of Ba due to the kinoshitalite substitution is observed in all sövites, although it is subordinate in the Badberg samples. Instead, Badberg biotites are strongly enriched in IVAl (eastonite substitution) which is less important in the other sövites. The compositional variations of apatite and mica within and between the different sövite bodies reflect the combined effects of fractional crystallization and carbonatite-wall rock interaction during emplacement. The latter process is especially important for the Badberg sövites, where metasomatic interaction released significant amounts of K, Fe, Ti, Al and Si from earlier crystallized nosean syenites. This resulted in a number of mineral reactions that transformed these rocks into calcite foidolites. Moreover, this triggered the crystallization of compositionally distinct mica and clinopyroxene crystals around the xenoliths and within the Badberg sövite itself. Thus, the presence and composition of clinopyroxene and mica in carbonatites may be useful indicators for contamination processes during their emplacement. Moreover, the local increase of silica activity during contamination enabled strong REE enrichment in apatite via a coupled substitution involving Si, which demonstrates the influence of contamination on REE mineralization in carbonatites.
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: 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.
Geochimica et Cosmochimica Acta, Vol. 277, pp. 224-242. pdf
Europe, Germany
carbonatite
Abstract: Studies of fluid inclusions in carbonatitic rocks are essential for understanding physicochemical processes involved in carbonatite-related hydrothermal ore mineralization and fenitization. However, the composition of many carbonatite-derived fluids is challenging to quantify, which hampers their detailed interpretation. Here, we present a systematic study of microthermometry of fluid inclusions found in carbonatites from the Kaiserstuhl (SW Germany), and a simple numerical model to estimate the compositions of such fluids, which are typical of numerous carbonatites worldwide. Four types of fluid inclusions have been identified in the Kaiserstuhl carbonatites: (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 high CO2 contents; and (IV) multi-component fluids with high salinity but little to no CO2. At present, it is only possible to quantify fluid compositions for types I and II. For the complex types III and IV, we conducted predictive modeling of the liquidus surface based on the Margules equations. The results suggest that carbonatite melts predominantly exsolve Na-K-sulfate-carbonate/bicarbonate-chloride brines (types III or IV). Such fluid inclusions may represent immiscible fluids that were trapped after segregation by boiling from a parental highly saline brine (type I). Fluid boiling, in turn, was probably triggered by a rapid pressure release during melt ascent. The present model enables quantification of fluid compositions associated with carbonatitic magmatism.
Geochimica et Cosmochimica Acta, Vol. 277, pp. 224-242. pdf
Europe, Germany
deposit - Kaiserstuhl
Abstract: Studies of fluid inclusions in carbonatitic rocks are essential for understanding physicochemical processes involved in carbonatite-related hydrothermal ore mineralization and fenitization. However, the composition of many carbonatite-derived fluids is challenging to quantify, which hampers their detailed interpretation. Here, we present a systematic study of microthermometry of fluid inclusions found in carbonatites from the Kaiserstuhl (SW Germany), and a simple numerical model to estimate the compositions of such fluids, which are typical of numerous carbonatites worldwide. Four types of fluid inclusions have been identified in the Kaiserstuhl carbonatites: (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 high CO2 contents; and (IV) multi-component fluids with high salinity but little to no CO2. At present, it is only possible to quantify fluid compositions for types I and II. For the complex types III and IV, we conducted predictive modeling of the liquidus surface based on the Margules equations. The results suggest that carbonatite melts predominantly exsolve Na-K-sulfate-carbonate/bicarbonate-chloride brines (types III or IV). Such fluid inclusions may represent immiscible fluids that were trapped after segregation by boiling from a parental highly saline brine (type I). Fluid boiling, in turn, was probably triggered by a rapid pressure release during melt ascent. The present model enables quantification of fluid compositions associated with carbonatitic magmatism.
Magmatic evolution and ascent history of the Aries micaceous kimberlite, central Kimberley Basin, Western Australia: evidence from zoned phlogopite phenocrysts and UV laser
Journal of Petrology, Vol. 47, 9, Sept. pp. 1751-1783.
Abstract: Two prominent features separate the Archean Wyoming and Hearne cratons: the Paleoproterozoic Great Falls tectonic zone (GFTZ) and the Medicine Hat block (MHB), neither of which is well defined spatially because of Phanerozoic sedimentary cover. Based on limited data, the MHB is thought to be a structurally complex mix of Archean (2.6-3.1?Ga) and Proterozoic (1.75?Ga) crust, but is recognized primarily by its geophysical signature, and its influence on the geochemistry of younger igneous rocks. Similarly, the GFTZ was recognized on the basis of broad differences in geophysical patterns, isopachs of Paleozoic sedimentary sections, and lineaments; however, juvenile arc rocks in the Little Belt Mountains (LBM) and strongly overprinted Archean rocks in southwestern Montana show it to be a dominantly Paleoproterozoic feature. The Little Rocky Mountains (LRM) of Montana provide access to exposures of the northeastern-most Precambrian crust in the MHB-GFTZ region. U/Pb ages of zircons from Precambrian rocks of the LRM range from 2.4 to 3.3?Ga, with most ages between 2.6 and 2.8?Ga. Whole-rock analyses yield Sm-Nd TDM from 3.1 to 4.0?Ga and initial eNd(T) values calculated at U-Pb zircon crystallization ages range from -0.9 to -10.5, indicating significant contributions from older Archean crust. The high proportion of 2.6-2.8?Ga U/Pb ages differentiates LRM crust from arc-related Paleoproterozoic magmatic rocks exposed in the LBM to the southwest. The age and isotopic composition of the LRM gneisses are similar to crust in the northern Wyoming Province (2.8-2.9?Ga), but Paleoproterozoic K-Ar cooling ages suggest crust in the LRM experienced the Paleoproterozoic metamorphism and deformation that characterizes the GFTZ. Consequently, its history differs markedly from the adjacent Beartooth-Bighorn magmatic zone of the northern Wyoming Province, which does not record Paleoproterozoic tectonism, but has a strong correlation with the Montana metasedimentary terrane that was strongly overprinted during the Paleoproterozoic Great Falls orogeny that defines the GFTZ. The LRM, therefore, likely provides a unique, and perhaps the only, opportunity to characterize Archean crust of the MHB.
Abstract: Strata in the Huron (2.5-2.0 Ga) and Animikie (2.2-1.85 Ga) basins were deposited on the southern margin of the Archean Superior province. These rocks were deformed during the Penokean orogeny (~1850 Ma) followed by subsequent accretionary orogens to the south at 1750 Ma (Yavapai) and 1630 Ma (Mazatzal). Strain patterns are unique to each orogenic belt with no far-field effect: Archean Wawa terrane rocks in the Penokean foreland preserve deformation associated with Archean accretion with no younger Penokean, Yavapai or Mazatzal strain overprint. The Penokean orogeny deformed Huron-Animikie basin sediments into a north-vergent fold-and-thrust belt with no Yavapai or Mazatzal strain overprint. Yavapai orogen strains (SW-NE margin-parallel shortening) are unique when compared to the younger Mazatzal shortening (N20°W) shortening, with no strain overprint. Penokean deformation is characterized by shortening from the south including uplifted Archean gneisses and a northerly thin-skinned fold-and-thrust belt, with north-vergent nappes and a gently-dipping foreland. Our study of finite and calcite twinning strains (n=60) along (~1500 km) and across (~200 km) the Penokean belt indicate that this orogeny was collisional as layer-parallel shortening axes are parallel across the belt, or parallel to the tectonic transport direction (~N-S). Penokean nappe burial near the margin resulted in vertical shortening strain overprints, some of which are layer-normal. The Sudbury impact layer (1850 Ma) is found across the Animikie basin and provides a widespread deformation marker with many local, unique strain observations. We also report new geochronology (U-Pb zircon and apatite) for the gneiss-mafic dike rocks at Wissota (Chippewa Falls, WI) and Arbutus (Black River Falls, WI) dams, respectively, which bears on Penokean-Yavapai deformation in the Archean Marshfield terrane which was accreted during the Penokean orogen. Pseudotachylite formation was common in the Superior province Archean basement rocks, especially along terrane boundaries reactivated by contemporaneous Penokean, Trans-Hudson, Cape Smith and New Quebec deformation. In the hinterland (south), the younger Yavapai orogen (1750 Ma; n=8) deformation is preserved as margin-parallel horizontal shortening (~SW-NE) in Yavapai crust and up to 200 km to the north in the Penokean thrust belt as a strain and Barrovian metamorphic overprint. Mazatzal deformation (1630 Ma; n=16) is preserved in quartzites on Yavapai and Penokean crust with layer-parallel and layer-normal shortening strains oriented N20°W.
Abstract: The subcontinental lithospheric mantle (SCLM) constitutes a significant portion of the upper mantle sourcing magmatic volatiles to the continents above, yet its geochemical signature and evolution remain poorly constrained. Here we present new interpretation of noble gas datasets from two magmatic CO2 fields in the SW US, namely Bravo Dome and Sheep Mountain, which provide a unique insight into the volatile character of the SCLM sourcing the Cenozoic volcanism in the region. We identify that reduction of 3He/4Hemantle ratio within the Sheep Mountain CO2 field can be attributed to radiogenic production within the SCLM. Using a Reduced Chi-Squared minimisation on the variation of derived 4He/21Necrust ratios within samples from the Sheep Mountain field, combined with a radiogenically raised 21Ne/22Nemantle end member, we resolve 3He/4Hemantle ratios of 2.59 ± 0.15 to 3.00 ± 0.18 Ra. These values correspond with a 21Ne/22Nemantle value of 0.136. Using these 3He/4Hemantle end member values with 21Nemantle resolved from Ne three component analysis, we derive the elemental 3He/22Nemantle of 2.80 ± 0.16 and radiogenic 4He/21Ne*mantle range of 1.11 ± 0.11 to 1.30 ± 0.14. A second Reduced Chi-Squared minimisation performed on the variation of 21Ne/40Arcrust ratios has allowed us to also determine both the 4He/40Armantle range of 0.78 to 1.21 and 21Ne/40Armantle of 7.66 ± 1.62 to 7.70 ± 1.54 within the field. Combining these ratios with the known mantle production ranges for 4He/21Ne and 4He/40Ar allows resolution of the radiogenic He/Ne and He/Ar ratios corresponding to the radiogenically lowered 3He/4Hemantle ratios. Comparing these values with those resolved from the Bravo Dome field allows identification of a clear and coherent depletion of He to Ne and He to Ar in both datasets. This depletion can only be explained by partial degassing of small melt fractions of asthenospheric melts that have been emplaced into the SCLM. This is the first time that it has been possible to resolve and account for both the mantle He/Ne and He/Ar ratios within a SCLM source. The data additionally rule out the involvement of a plume component in the mantle source of the two gas fields and hence any plume influence on the Colorado Plateau Uplift event.
Abstract: The study of sediment cores allows for the reconstruction of past climate and environment through physical-chemical analysis. Nevertheless, this interpretation suffers from many drawbacks that can be overcome with the newest technologies. Hyperspectral imaging is one of these and allows a fast, high resolution, and non-destructive analysis of sediment cores. In this study, we use visible and near-infrared hyperspectral imaging to predict particle size fractions and distribution (PSD) at a resolution of 200?µm on a previously well-studied sediment core taken from Lake Bourget (Western Alps, France). These predictions agree with previous studies on this core. Then, the PSD was used to estimate sedimentary deposit sources using the PSD unmixing algorithm AnalySize. It permitted estimation of the contribution of five sources (micrite, small and large bio-induced calcite crystals, diatom frustules, detrital particles), which had previously been characterized. The spatial dimension allowed for laminae to be discretized and counted, in agreement with the age-depth model previously established. We then evaluated the particle size and spectral signatures of each of these annual laminae, hence characterizing their physico-chemical composition. These high-resolution data also allowed for estimation of the accumulation rate (cm/year) of each of the main sources in the laminated unit and inferring the trophic status and the presence of instantaneous events of the lake.
Abstract: Across much of North America, the contact between Precambrian basement and Paleozoic strata is the Great Unconformity, a surface that represents a >0.4 b.y.-long hiatus. A digital elevation model (DEM) of this surface visually highlights regional-scale variability in the character of basement topography across the United States cratonic platform. Specifically, it delineates Phanerozoic tectonic domains, each characterized by a distinct structural wavelength (horizontal distance between adjacent highs) and/or structural amplitude (vertical distance between adjacent lows and highs). The largest domain, the Midcontinent domain, includes long-wavelength epeirogenic basins and domes, as well as fault-controlled steps. The pronounced change in land-surface elevation at the Rocky Mountain Front coincides with the western edge of the Midcontinent domain on the basement DEM. In the Rocky Mountain and Colorado Plateau domains, west of the Rocky Mountain Front, structural wavelength is significantly shorter and structural amplitude significantly higher than in the Midcontinent domain. The Bordering Basins domain outlines the southern and eastern edges of the Midcontinent domain. As emphasized by the basement DEM, several kilometers of structural relief occur across the boundary between these two domains, even though this boundary does not stand out on ground-surface topography. A plot of epicenters on the basement DEM supports models associating intraplate seismicity with the Midcontinent domain edge. Notably, certain changes in crustal thickness also coincide with distinct changes in basement depth.
Journal of the Geological Society of London, in press available 25p.
Africa, Madagascar
thermochronology
Abstract: Madagascar occupied an important place in the amalgamation of Gondwana, and preserves a record of several Neoproterozoic events that can be linked to orogenesis of the East African Orogen. We integrate remote sensing and field data to unravel complex deformation in the Ikalamavony and Itremo domains of central Madagascar. The deformation sequence comprises a gneissic foliation (S1), followed by south to south-west directed, tight to isoclinal, recumbent folding (D2). These are overprinted by north-trending upright folds that formed during a ~E-W shortening event. Together these produced type 1 and type 2 fold interference patterns throughout the Itremo and Ikalamavony domains. Apatite U-Pb and muscovite and biotite Rb-Sr thermochronometers indicate that much of central Madagascar was thermally reset to at least ~500oC at c. 500 Ma. Deformation in west-central Madagascar occurred between c. 750 Ma and c. 550 Ma, and we suggest this deformation formed in response to the c. 650 Ma collision of Azania with Africa along the Vohibory Suture in southwestern Madagascar. In eastern Madagascar, deformation is syn- to post-550 Ma, which formed in response to the final closure of the Mozambique Ocean along the Betsimisaraka Suture that amalgamated Madagascar with the Dharwar Craton of India.
Journal of the Geological Society, Vol. 177, pp. 784-798.
Africa, Madagascar
geothermometry
Abstract: Madagascar occupied an important place in the amalgamation of Gondwana and preserves a record of several Neoproterozoic events that are linked to orogenesis of the East African Orogen. In this study, we integrate remote sensing, field data and thermochronology to unravel complex deformation in the Ikalamavony and Itremo domains of central Madagascar. The deformation sequence comprises a gneissic foliation (S1), followed by south- to SW-directed, tight to isoclinal, recumbent folding (D2). These are overprinted by north-trending upright folds that formed during an approximately east-west shortening event (D3). Together these produced type 1 and type 2 fold interference patterns throughout the Itremo and Ikalamavony domains. We show that the Itremo and Ikalamavony domains were deformed together in the same orogenic system, which we interpret as the c. 630 Ma collision of Azania with Africa along the Vohibory Suture in southwestern Madagascar. In eastern Madagascar, deformation is syn- to post-550 Ma, and probably formed in response to final closure of the Mozambique Ocean along the Betsimisaraka Suture that amalgamated Madagascar with the Dharwar Craton of India. Apatite U-Pb and novel laser ablation triple quadrupole inductively coupled plasma mass spectrometry (LA-QQQ-ICP-MS) muscovite and biotite Rb-Sr thermochronology indicates that much of central Madagascar cooled through c. 500°C at c. 500 Ma.
Geological Society of London Special Publication Supercontinent Cycles through Earth History., Vol. 424, pp. 47-81.
Australia
Supercontinents
Abstract: The Australian continent records c. 1860-1800 Ma orogenesis associated with rapid accretion of several ribbon micro-continents along the southern and eastern margins of the proto-North Australian Craton during Nuna assembly. The boundaries of these accreted micro-continents are imaged in crustal-scale seismic reflection data, and regional gravity and aeromagnetic datasets. Continental growth (c. 1860-1850 Ma) along the southern margin of the proto-North Australian Craton is recorded by the accretion of a micro-continent that included the Aileron Terrane (northern Arunta Inlier) and the Gawler Craton. Eastward growth of the North Australian Craton occurred during the accretion of the Numil Terrane and the Abingdon Seismic Province, which forms part of a broader zone of collision between the northwestern margins of Laurentia and the proto-North Australian Craton. The Tickalara Arc initially accreted with the Kimberley Craton at c. 1850 Ma and together these collided with the proto-North Australian Craton at c. 1820 Ma. Collision between the West Australian Craton and the proto-North Australian Craton at c. 1790-1760 Ma terminated the rapid growth of the Australian continent.
Abstract: Southern Africa is characterised by unusually elevated topography and abnormal heat flow. This can be explained by thermal perturbation of the mantle, but the origin of this is unclear. Geophysics has not detected a thermal anomaly in the upper mantle and there is no geochemical evidence of an asthenosphere mantle contribution to the Cenozoic volcanic record of the region. Here we show that natural CO2 seeps along the Ntlakwe-Bongwan fault within KwaZulu-Natal, South Africa, have C-He isotope systematics that support an origin from degassing mantle melts. Neon isotopes indicate that the melts originate from a deep mantle source that is similar to the mantle plume beneath Réunion, rather than the convecting upper mantle or sub-continental lithosphere. This confirms the existence of the Quathlamba mantle plume and importantly provides the first evidence in support of upwelling deep mantle beneath Southern Africa, helping to explain the regions elevation and abnormal heat flow.
Moteani, G., Kostitsyn, Y.A., Gilg, H.A., Preinfalk, C., Razakamanana, T.
Geochemistry of phlogopite, diopside, calcite, anhydrite and apatite pegmatites and syenites of southern Madagascar: evidence for crustal silicocarbonatitic (CSC) melt formatio in a Panafrican collisional tectonic setting.
International Journal of Earth Sciences, Vol. 102, 3, pp. 627-645.
Abstract: Chemical and microscopic examination of the first gem-quality synthetic emeralds of facetable size proves that Prof. Richard Nacken grew two main types of emerald by flux methods in the mid-1920s. One of these two types, grown with colorless beryl seeds in molybdenum-bearing and vanadium-free fluxes, has not previously been mentioned in the literature and would appear to be unknown to gemologists. The other main type, which has already been described in gemological publications, was grown from molybdenum- and vanadium-bearing fluxes. In drawing these conclusions, rough and faceted synthetic emeralds produced by Nacken were available for study from two principal sources: the Deutsches Museum in Munich, to which Nacken had donated samples in 1961, and family members who had inherited such crystals. Chemical, morphological, and microscopic properties are given, and circumstances concerning the developmental history of the Nacken production, including the possibility of collaboration with IG Farben (a subject of past speculation), are discussed as well. The latter has recently been elucidated by the discovery of original documents from the IG Farben gemstone plant, preserved in the Archives of the German Federal State of Saxony-Anhalt.
Abstract: Much of the secular record of sulfur mass independet fractionation (S-MIF) is based on pyrites extracted from a limited number of formations from Western Australia and Southern Africa. Here we present multiproxy evidence for an episodic loss of S-MIF in sulfides from a 2.7 Ga sedimentary record in the Săo Francisco craton, Brazil. Based on combined proxies, we assigned three phases, in a continous drill core, that track evolving water column redox conditions and changes in ecology. In Phase-I, the stratigraphically older rocks, reactive iron ratios suggest ferruginous conditions. The pyrites have modest S-MIF values (D33S from -0.7 to 2.6‰) and the carbon isotope composition of the iron formations is indicative of carbon fixation by anoxygenic photosynthetic bacteria that oxidized Fe2+ (d13Corg from -27.7 to -17.5‰). Within Phase-II, an intermediate phase characterized by graphite schist, the iron ratios, expansion of the S-MIF (D33S from 2.15 to 3.4‰) and an excess of Mo relative to Corg suggest deposition in an anoxic environment with periodic development of euxinic conditions. Phase-III culminates in fully oxic conditions with a loss of S-MIF and emergence of sulfur mass dependent fractionation (S-MDF) with homogeneous d34S pyrite values (average = 3.3 ± 0.5‰). The loss of S-MIF in the Archean sulfides of Phase-III was interpreted as a response to increased oxygen levels that lead to an intensification of oxidative weathering. Based on the continous deposition within this drillcore, the development of more oxidizing conditions may have been relatively rapid, reinforcing the model that the transition from S-MIF to S-MDF can happen on rapid geological time scales and was recorded about 400 million years prior to the GOE in the Brazilian craton.
The Frimingen garnet peridotite ( central Swedish Caledonides). A good example of the characteristic PTt path of a cold mantle wedge garnet peridotite.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 97.
Canada, Northwest Territories
legal
Abstract: Established in 1999, the Diamond Policy Framework (DPF) was designed to facilitate the development of a diamond manufacturing industry in the Northwest Territories (NWT). In addition, agreements with NWT diamond producers were established which required them to offer 10 percent of their production, by value, to Approved NWT Diamond Manufacturers (ANDM) for manufacturing in the NWT. The NWT is the most expensive jurisdiction in which to operate a manufacturing facility and despite some early success, the policy was not successful in creating an operating environment for the secondary industry to flourish. In 2018, ITI commissioned a review of the DPF that sought recommendations on how to make this industry more attractive to investors. The report contained a detailed review of the global diamond market. It also presented a series of cost per carat analyses of NWT production costs versus costs in other diamond manufacturing regions. Policy recommendations included adopting an export provision for NWT rough diamonds (and making that export volume contingent on their investment in the NWT), permitting the development of a facility for high-skill planning and lasering services, and generally ensuring that the policy supported the acceptance of innovative business plans. In 2018, The Department of Industry, Tourism and Investment (ITI) amended the DPF. Accordingly, a new approach to the utilization of rough diamonds was developed to realize maximum economic benefits for the NWT and its residents. The amended DPF now has provisions that allow an ANDM to export a portion of their allocation based on their business proposal and an ANDM is no longer required to complete the entire manufacturing process in the NWT. To be eligible to export rough diamonds, ANDM applicants must provide a comprehensive business plan that outlines investment details. Business plans are reviewed and scored based on a comprehensive matrix that determines the export volume.
Journal of the Geological Society of London, in press available 25p.
Africa, Madagascar
thermochronology
Abstract: Madagascar occupied an important place in the amalgamation of Gondwana, and preserves a record of several Neoproterozoic events that can be linked to orogenesis of the East African Orogen. We integrate remote sensing and field data to unravel complex deformation in the Ikalamavony and Itremo domains of central Madagascar. The deformation sequence comprises a gneissic foliation (S1), followed by south to south-west directed, tight to isoclinal, recumbent folding (D2). These are overprinted by north-trending upright folds that formed during a ~E-W shortening event. Together these produced type 1 and type 2 fold interference patterns throughout the Itremo and Ikalamavony domains. Apatite U-Pb and muscovite and biotite Rb-Sr thermochronometers indicate that much of central Madagascar was thermally reset to at least ~500oC at c. 500 Ma. Deformation in west-central Madagascar occurred between c. 750 Ma and c. 550 Ma, and we suggest this deformation formed in response to the c. 650 Ma collision of Azania with Africa along the Vohibory Suture in southwestern Madagascar. In eastern Madagascar, deformation is syn- to post-550 Ma, which formed in response to the final closure of the Mozambique Ocean along the Betsimisaraka Suture that amalgamated Madagascar with the Dharwar Craton of India.
Journal of the Geological Society, Vol. 177, pp. 784-798.
Africa, Madagascar
geothermometry
Abstract: Madagascar occupied an important place in the amalgamation of Gondwana and preserves a record of several Neoproterozoic events that are linked to orogenesis of the East African Orogen. In this study, we integrate remote sensing, field data and thermochronology to unravel complex deformation in the Ikalamavony and Itremo domains of central Madagascar. The deformation sequence comprises a gneissic foliation (S1), followed by south- to SW-directed, tight to isoclinal, recumbent folding (D2). These are overprinted by north-trending upright folds that formed during an approximately east-west shortening event (D3). Together these produced type 1 and type 2 fold interference patterns throughout the Itremo and Ikalamavony domains. We show that the Itremo and Ikalamavony domains were deformed together in the same orogenic system, which we interpret as the c. 630 Ma collision of Azania with Africa along the Vohibory Suture in southwestern Madagascar. In eastern Madagascar, deformation is syn- to post-550 Ma, and probably formed in response to final closure of the Mozambique Ocean along the Betsimisaraka Suture that amalgamated Madagascar with the Dharwar Craton of India. Apatite U-Pb and novel laser ablation triple quadrupole inductively coupled plasma mass spectrometry (LA-QQQ-ICP-MS) muscovite and biotite Rb-Sr thermochronology indicates that much of central Madagascar cooled through c. 500°C at c. 500 Ma.
Proceedings of National Academy of Science USA, Vol. 113, 40, pp. 11127-11130.
Mantle
Iron
Abstract: We performed laser-heated diamond anvil cell experiments combined with state-of-the-art electron microanalysis (focused ion beam and aberration-corrected transmission electron microscopy) to study the distribution and valence of iron in Earth’s lower mantle as a function of depth and composition. Our data reconcile the apparently discrepant existing dataset, by clarifying the effects of spin (high/low) and valence (ferrous/ferric) states on iron partitioning in the deep mantle. In aluminum-bearing compositions relevant to Earth’s mantle, iron concentration in silicates drops above 70 GPa before increasing up to 110 GPa with a minimum at 85 GPa; it then dramatically drops in the postperovskite stability field above 116 GPa. This compositional variation should strengthen the lowermost mantle between 1,800 km depth and 2,000 km depth, and weaken it between 2,000 km depth and the D” layer. The succession of layers could dynamically decouple the mantle above 2,000 km from the lowermost mantle, and provide a rheological basis for the stabilization and nonentrainment of large low-shear-velocity provinces below that depth.
Proceedings of National Academy of Science USA, Vol. 113, no. 40, pp. 11127-11130.
Mantle
UHP
Abstract: We performed laser-heated diamond anvil cell experiments combined with state-of-the-art electron microanalysis (focused ion beam and aberration-corrected transmission electron microscopy) to study the distribution and valence of iron in Earth's lower mantle as a function of depth and composition. Our data reconcile the apparently discrepant existing dataset, by clarifying the effects of spin (high/low) and valence (ferrous/ferric) states on iron partitioning in the deep mantle. In aluminum-bearing compositions relevant to Earth's mantle, iron concentration in silicates drops above 70 GPa before increasing up to 110 GPa with a minimum at 85 GPa; it then dramatically drops in the postperovskite stability field above 116 GPa. This compositional variation should strengthen the lowermost mantle between 1,800 km depth and 2,000 km depth, and weaken it between 2,000 km depth and the D" layer. The succession of layers could dynamically decouple the mantle above 2,000 km from the lowermost mantle, and provide a rheological basis for the stabilization and nonentrainment of large low-shear-velocity provinces below that depth.
Earth and Planteray Science Letters, Vol. 489, pp. 84-91.
Mantle
carbonate
Abstract: Carbonate minerals are important hosts of carbon in the crust and mantle with a key role in the transport and storage of carbon in Earth's deep interior over the history of the planet. Whether subducted carbonates efficiently melt and break down due to interactions with reduced phases or are preserved to great depths and ultimately reach the core-mantle boundary remains controversial. In this study, experiments in the laser-heated diamond anvil cell (LHDAC) on layered samples of dolomite (Mg,?Ca)CO3 and iron at pressure and temperature conditions reaching those of the deep lower mantle show that carbon-iron redox interactions destabilize the MgCO3 component, producing a mixture of diamond, Fe7C3, and (Mg,?Fe)O. However, CaCO3 is preserved, supporting its relative stability in carbonate-rich lithologies under reducing lower mantle conditions. These results constrain the thermodynamic stability of redox-driven breakdown of carbonates and demonstrate progress towards multiphase mantle petrology in the LHDAC at conditions of the lowermost mantle.
Nature Communications, doe:10.1038/ s41467-018- 030808-6 6p. Pdf
Technology
ureilite
Abstract: Planetary formation models show that terrestrial planets are formed by the accretion of tens of Moon- to Mars-sized planetary embryos through energetic giant impacts. However, relics of these large proto-planets are yet to be found. Ureilites are one of the main families of achondritic meteorites and their parent body is believed to have been catastrophically disrupted by an impact during the first 10 million years of the solar system. Here we studied a section of the Almahata Sitta ureilite using transmission electron microscopy, where large diamonds were formed at high pressure inside the parent body. We discovered chromite, phosphate, and (Fe,Ni)-sulfide inclusions embedded in diamond. The composition and morphology of the inclusions can only be explained if the formation pressure was higher than 20?GPa. Such pressures suggest that the ureilite parent body was a Mercury- to Mars-sized planetary embryo.
Dorfman, S.M., Potapkin, V., Lv, M., Greenberg, E., Kupenko, I., Chumakov, A.I., Bi, W., Alp, E.E., Liu, J., Magrez, A., Dutton, S.E., Cava, R.J., McCammon, C.A., Gillet, P.
American Mineralogist, Vol. 105, pp. 1030-1039. pdf
Mantle
redox
Abstract:
Electronic states of iron in the lower mantle's dominant mineral, (Mg,Fe,Al)(Fe,Al,Si)O3 bridgmanite, control physical properties of the mantle including density, elasticity, and electrical and thermal conductivity. However, the determination of electronic states of iron has been controversial, in part due to different interpretations of Mössbauer spectroscopy results used to identify spin state, valence state, and site occupancy of iron. We applied energy-domain Mössbauer spectroscopy to a set of four bridgmanite samples spanning a wide range of compositions: 10-50% Fe/total cations, 0-25% Al/total cations, 12-100% Fe3+/total Fe. Measurements performed in the diamond-anvil cell at pressures up to 76 GPa below and above the high to low spin transition in Fe3+ provide a Mössbauer reference library for bridgmanite and demonstrate the effects of pressure and composition on electronic states of iron. Results indicate that although the spin transition in Fe3+ in the bridgmanite B-site occurs as predicted, it does not strongly affect the observed quadrupole splitting of 1.4 mm/s, and only decreases center shift for this site to 0 mm/s at ~70 GPa. Thus center shift can easily distinguish Fe3+ from Fe2+ at high pressure, which exhibits two distinct Mössbauer sites with center shift ~1 mm/s and quadrupole splitting 2.4-3.1 and 3.9 mm/s at ~70 GPa. Correct quantification of Fe3+/total Fe in bridgmanite is required to constrain the effects of composition and redox states in experimental measurements of seismic properties of bridgmanite. In Fe-rich, mixed-valence bridgmanite at deep-mantle-relevant pressures, up to ~20% of the Fe may be a Fe2.5+ charge transfer component, which should enhance electrical and thermal conductivity in Fe-rich heterogeneities at the base of Earth's mantle.
Journal of Geophysical Research,, Vol. 121, 7, pp. 5013-5030.
Canada
Subduction
Abstract: The cratonic cores of the continents are remarkably stable and long-lived features. Their ability to resist destructive tectonic processes is associated with their thick (~250 km), cold, chemically depleted, buoyant lithospheric keels that isolate the cratons from the convecting mantle. The formation mechanism and tectonic stability of cratonic keels remains under debate. To address this issue, we use P wave and S wave relative arrival-time tomography to constrain upper mantle structure beneath southeast Canada and the northeast USA, a region spanning three quarters of Earth's geological history. Our models show three distinct, broad zones: Seismic wave speeds increase systematically from the Phanerozoic coastal domains, through the Proterozoic Grenville Province, and to the Archean Superior craton in central Québec. We also recover the NW-SE trending track of the Great Meteor hot spot that crosscuts the major tectonic domains. The decrease in seismic wave speed from Archean to Proterozoic domains across the Grenville Front is consistent with predictions from models of two-stage keel formation, supporting the idea that keel growth may not have been restricted to Archean times. However, while crustal structure studies suggest that Archean Superior material underlies Grenvillian age rocks up to ~300 km SE of the Grenville Front, our tomographic models show a near-vertical boundary in mantle wave speed directly beneath the Grenville Front. We interpret this as evidence for subduction-driven metasomatic enrichment of the Laurentian cratonic margin, prior to keel stabilization. Variable chemical depletion levels across Archean-Proterozoic boundaries worldwide may thus be better explained by metasomatic enrichment than inherently less depleted Proterozoic composition at formation.
Earth and Planetary Science Letters, Vol. 479, pp. 170-178.
Canada, Nunavut, Baffin Island
geophysics - seismics
Abstract: The northern Hudson Bay region in Canada comprises several Archean cratonic nuclei, assembled by a number of Paleoproterozoic orogenies including the Trans-Hudson Orogen (THO) and the Rinkian-Nagssugtoqidian Orogen. Recent debate has focused on the extent to which these orogens have modern analogues such as the Himalayan-Karakoram-Tibet Orogen. Further, the structure of the lithospheric mantle beneath the Hudson Strait and southern Baffin Island is potentially indicative of Paleoproterozoic underthrusting of the Superior plate beneath the Churchill collage. Also in question is whether the Laurentian cratonic root is stratified, with a fast, depleted, Archean core underlain by a slower, younger, thermally-accreted layer. Plate-scale process that create structures such as these are expected to manifest as measurable fossil seismic anisotropic fabrics. We investigate these problems via shear wave splitting, and present the most comprehensive study to date of mantle seismic anisotropy in northern Laurentia. Strong evidence is presented for multiple layers of anisotropy beneath Archean zones, consistent with the episodic development model of stratified cratonic keels. We also show that southern Baffin Island is underlain by dipping anisotropic fabric, where underthrusting of the Superior plate beneath the Churchill has previously been interpreted. This provides direct evidence of subduction-related deformation at 1.8 Ga, implying that the THO developed with modern plate-tectonic style interactions.
Journal of Geophysical Research, Vol. 123, 7, pp. 5690-5709.
Canada, Nunavut
Geophysics - seismic
Abstract: The geology of northern Hudson Bay, Canada, documents more than 2 billion years of history including the assembly of Precambrian and Archean terranes during several Paleoproterozoic orogenies, culminating in the Trans-Hudson Orogen (THO) ~1.8 Ga. The THO has been hypothesized to be similar in scale and nature to the ongoing Himalaya-Karakoram-Tibetan orogen, but the nature of lithospheric terrane boundaries, including potential plate-scale underthrusting, is poorly understood. To address this problem, we present new P and S wave tomographic models of the mantle seismic structure using data from recent seismograph networks stretching from northern Ontario to Nunavut (60-100°W and 50-80°N). The large size of our network requires careful mitigation of the influence of source side structure that contaminates our relative arrival time residuals. Our tomographic models reveal a complicated internal structure in the Archean Churchill plate. However, no seismic wave speed distinction is observed across the Snowbird Tectonic Zone, which bisects the Churchill. The mantle lithosphere in the central region of Hudson Bay is distinct from the THO, indicating potential boundaries of microcontinents and lithospheric blocks between the principal colliders. Slow wave speeds underlie southern Baffin Island, the leading edge of the generally high wave speed Churchill plate. This is interpreted to be Paleoproterozoic material underthrust beneath Baffin Island in a modern-style subduction zone setting.
Journal of Geophysical Research: Solid Earth, in press available, 24p. Pdf
Canada
geophysics - seismics
Abstract: The geological record of SE Canada spans more than 2.5Ga, making it a natural laboratory for the study of crustal formation and evolution over time. We estimate the crustal thickness, Poisson's ratio, a proxy for bulk crustal composition, and shear velocity (Vs) structure from receiver functions at a network of seismograph stations recently deployed across the Archean Superior craton, the Proterozoic Grenville and the Phanerozoic Appalachian provinces. The bulk seismic crustal properties and shear velocity structure reveal a correlation with tectonic provinces of different ages: the post-Archean crust becomes thicker, faster, more heterogenous and more compositionally evolved. This secular variation pattern is consistent with a growing consensus that crustal growth efficiency increased at the end of the Archean. A lack of correlation among elevation, Moho topography, and gravity anomalies within the Proterozoic belt is better explained by buoyant mantle support rather than by compositional variations driven by lower crustal metamorphic reactions. A ubiquitous ~20km thick high-Vs lower-crustal layer is imaged beneath the Proterozoic belt. The strong discontinuity at 20km may represent the signature of extensional collapse of an orogenic plateau, accommodated by lateral crustal flow. Wide anorthosite massifs inferred to fractionate from a mafic mantle source are abundant in Proterozoic geology and are underlain by high Vs lower crust and a gradational Moho. Mafic underplating may have provided a source for these intrusions and could have been an important post-Archean process stimulating mafic crustal growth in a vertical sense.
Abstract: Although plate tectonics has pushed the frontiers of geosciences in the past 50 years, it has legitimate limitations and among them we focus on both the absence of dynamics in the theory, and the difficulty of reconstructing tectonics when data is sparse. In this manuscript, we propose an anticipation experiment, proposing a singular outlook on plate tectonics in the digital era. We hypothesize that mantle convection models producing self-consistently plate-like behavior will capture the essence of the self-organisation of plate boundaries. Such models exist today in a preliminary fashion and we use them here to build a database of mid-ocean ridge and trench configurations. To extract knowledge from it we develop a machine learning framework based on Generative Adversarial Networks (GANs) that learns the regularities of the self-organisation in order to fill gaps of observations when working on reconstructing a plate configuration. The user provides the distribution of known ridges and trenches, the location of the region where observations lack, and our digital architecture proposes a horizontal divergence map from which missing plate boundaries are extracted. Our framework is able to prolongate and interpolate plate boundaries within an unresolved region, but fails to retrieve a plate boundary that would be completely contained inside of it. The attempt we make is certainly too early because geodynamic models need improvement and a larger amount of geodynamic model outputs, as independent as possible, is required. However, this work suggests applying such an approach to expand the capabilities of plate tectonics is within reach.
Abstract: Limited field studies and sparse chronological constraints in the southwestern Great Slave Lake area creates uncertainties about the Laurentide Ice Sheet (LIS) flow history and deglacial chronology. Improved understanding of the western LIS ice-margin morphology and retreat history is required to refine larger ice-sheet interpretations and timing for northwest drainage of glacial Lake McConnell. Using new field observations and geochronology we establish ice-flow history and better constrain regional deglaciation. Paleo-ice flow indicators (n = 66) show an oldest southwestern flow (230°), an intermediate northwesterly flow (305°), and a youngest westerly flow (250°). Till samples bulk sediment and matrix properties (n = 160) allowed identification of two till units. A lower grey till sourced mainly from local Paleozoic sediments produced clast fabrics indicating a southwesterly flow direction, overlain by a brown till that contained an increased Canadian Shield content with lodged elongate boulders a-axes and boulder-top striation orientations indicating a west to northwest ice-flow direction. Ice-flow results show a clockwise shift in direction interpreted as evidence for ice-divide migration followed by topographically controlled deglacial westward flow influenced by the Mackenzie River valley. Minimum deglacial timing estimates were constrained through optical dating of fine-sand deposits in a well-developed strandline (n = 2) and seven aeolian dunes; ages range from 9.9 ± 0.6 to 10.8 ± 0.7 ka BP. These ages are from dunes located below glacial Lake McConnell maximum water level and may thus provide new local lake level age constraints. Ice retreat is informed by a newly-mapped segment of the Snake River moraine, which is an understudied feature in the region. New ice-flow history and ice-margin retreat interpretations will be integrated into the larger body of work on the western LIS providing more confident conclusions on ice-sheet evolution and meltwater drainage pathways, specifically in the southwestern Great Slave Lake area.
Abstract: The thermophysical properties of silicate melts and glasses are of fundamental importance for the characterization of the dynamics and energetics of silicate melts on Earth and terrestrial planets. The heat capacity of silicate melts is of particular importance because of its implications for the temperature dependencies of melt enthalpy and entropy and for the potential relationship to melt structure and transport properties. Currently, there are reliable models for predicting the heat capacity of simple and multicomponent silicate glasses (Cpglass) as a function of composition and temperature. Recent differential scanning calorimetry (DSC) measurements of heat capacity for multicomponent silicate liquid (Cpliquid), however, have shown that published models do not accurately reproduce heat capacity measurements on some silicate melts. Here, we have compiled a database of heat capacity values for hydrous and anhydrous multicomponent natural samples. The measurements are on pairs of glasses and melts over the compositional range (wt%) of: SiO2 (44-79), Al2O3 (5-35), TiO2 (0-3), FeOtot (0 - 11); Na2O + K2O (0-27); CaO + MgO (0-39), H2O (0-6.3) and minor oxides. The compiled data show strong correlations between silica content (XSiO2) and the configurational heat capacity (Cpconfig) defined as Cpliquid - Cpglass measured across the glass transition temperature (Tg). This correlation is used to establish an empirical model for predicting Cpliquid as a function of melt composition (i.e. SiO2 content) and values of Cpglass measured at the onset of the glass transition: Cpliquid=52.6-55.88XSiO2+CpglassCpliquid=52.6-55.88XSiO2+Cpglass. The model reproduces values of Cpliquid to within an average relative error of ~ 2.4%. Published models for the heat capacities of silicate melts (e.g., Stebbins, 1984; Richet and Bottinga, 1985; Lange and Navrotsky, 1992) applied to the same dataset have average relative errors in excess of 5.5%.
Earth and Planetary Science Letters, Vol. 501, pp. 202-212.
Mantle
melting
Abstract: The viscosity of silicate melts is the most important physical property governing magma transport and eruption dynamics. This macroscopic property is controlled by composition and temperature but ultimately reflects the structural organization of the melt operating at the microscale. At present, there is no explicit relationship connecting viscosity to silicate melt structure and vice versa. Here, we use a single Raman spectroscopic parameter, indicative of melt structure, to accurately forecast the viscosity of natural, multicomponent silicate melts from spectroscopic measurements on glasses preserved on Earth and other planets. The Raman parameter is taken as the ratio of low and high frequency vibrational bands from the silicate glass by employing a green source laser wavelength of 514.5 nm (R514.5). Our model is based on an empirical linkage between R514.5 and coefficients in the Vogel-Fulcher-Tammann function for the temperature dependence of melt viscosity. The calibration of the Raman-based model for melt viscosity is based on 413 high-temperature measurements of viscosity on 23 melt compositions for which published Raman spectra are available. The empirical model obviates the need for chemical measurement of glass compositions, thereby, providing new opportunities for tracking physical and thermochemical properties of melts during igneous processes (e.g., differentiation, mixing, assimilation). Furthermore, our model serves as a milepost for the future use of Raman spectral data for predicting transport (and calorimetric) properties of natural melts at geological conditions (e.g., volatiles and pressure) and production.
Earth and Planetary Science Letters, Vol. 501, pp. 202-212.
Mantle
melting
Abstract: The viscosity of silicate melts is the most important physical property governing magma transport and eruption dynamics. This macroscopic property is controlled by composition and temperature but ultimately reflects the structural organization of the melt operating at the microscale. At present, there is no explicit relationship connecting viscosity to silicate melt structure and vice versa. Here, we use a single Raman spectroscopic parameter, indicative of melt structure, to accurately forecast the viscosity of natural, multicomponent silicate melts from spectroscopic measurements on glasses preserved on Earth and other planets. The Raman parameter is taken as the ratio of low and high frequency vibrational bands from the silicate glass by employing a green source laser wavelength of 514.5 nm (R514.5). Our model is based on an empirical linkage between R514.5 and coefficients in the Vogel-Fulcher-Tammann function for the temperature dependence of melt viscosity. The calibration of the Raman-based model for melt viscosity is based on 413 high-temperature measurements of viscosity on 23 melt compositions for which published Raman spectra are available. The empirical model obviates the need for chemical measurement of glass compositions, thereby, providing new opportunities for tracking physical and thermochemical properties of melts during igneous processes (e.g., differentiation, mixing, assimilation). Furthermore, our model serves as a milepost for the future use of Raman spectral data for predicting transport (and calorimetric) properties of natural melts at geological conditions (e.g., volatiles and pressure) and production.
Gondwana Research, Vol. 70, pp. 1-24. doi:10.1016/ j.gr.2018.12.005
South America, Brazil
craton
Abstract: The study of Paleoproterozoic rocks is crucial for understanding Earth's tectonic evolution during the time when most of the modern crust and ore deposits were formed. The rocks of the Brazilian Amazonian Craton record some of the most-complete and best-preserved Paleoproterozoic magmatic and volcanic episodes on Earth. Following previous investigations, we present new lithofaciological and stratigraphic records of the felsic rocks of the Tapajós Mineral Province (TMP) (~2-1.88?Ga) and the Săo Felix do Xingú region (SFX) (~1.88?Ga) which, combined with new petrological and geochronological data, help providing a more complete understanding of the tectonic, magmatic and volcanological evolution of the Amazonian Craton. This magmatism/volcanism is thought to be formed in a late-/post-orogenic to extentional regime confirmed by the new geochemical data presented here. The transition from late-convergent to extensional tectonic setting could register the beginning of the taphrogenesis that marked the Amazonian Craton throughout the Mesoproterozoic. The volcanological approach of this contribution can serve as a strategy for the modelling of the evolution of Precambrian volcano-sedimentary basins around the world. The large amount of rocks analyzed are divided into primary and secondary volcaniclastic products depending on if they resulted from a direct volcanic activity (pyroclastic) or processes that reworked pyroclastic fragments. Furthermore, the deposits are subdivided into massive and stratified, depending on their primary mechanisms of transport and emplacement. By confirming the results from previous studies, our study permits to depict a more precise paleo-environmental picture of the processes that occurred in the Amazonian Craton during the Late-Paleoproterozoic. In particular, the presence of large regional-scale fissural systems and caldera collapses produced large silicic explosive volcanic eruptions, also accompanied by the emission of large volume effusive products. Although studies on the Amazonian Craton are still scarce and controversial, the present study provides new evidence that this volcanism may have formed one of the largest Silicic Large Igneous Provinces (SLIP) on earth. Our data also confirm that at least two major Paleoproterozoic periods of formation of volcanic rocks exist in the Amazonian craton. This point is of great relevance for any future interpretation of the geological evolution of this craton.
Abstract: The study of Paleoproterozoic rocks is crucial for understanding Earth's tectonic evolution during the time when most of the modern crust and ore deposits were formed. The rocks of the Brazilian Amazonian Craton record some of the most-complete and best-preserved Paleoproterozoic magmatic and volcanic episodes on Earth. Following previous investigations, we present new lithofaciological and stratigraphic records of the felsic rocks of the Tapajós Mineral Province (TMP) (~2-1.88?Ga) and the Săo Felix do Xingú region (SFX) (~1.88?Ga) which, combined with new petrological and geochronological data, help providing a more complete understanding of the tectonic, magmatic and volcanological evolution of the Amazonian Craton. This magmatism/volcanism is thought to be formed in a late-/post-orogenic to extentional regime confirmed by the new geochemical data presented here. The transition from late-convergent to extensional tectonic setting could register the beginning of the taphrogenesis that marked the Amazonian Craton throughout the Mesoproterozoic. The volcanological approach of this contribution can serve as a strategy for the modelling of the evolution of Precambrian volcano-sedimentary basins around the world. The large amount of rocks analyzed are divided into primary and secondary volcaniclastic products depending on if they resulted from a direct volcanic activity (pyroclastic) or processes that reworked pyroclastic fragments. Furthermore, the deposits are subdivided into massive and stratified, depending on their primary mechanisms of transport and emplacement. By confirming the results from previous studies, our study permits to depict a more precise paleo-environmental picture of the processes that occurred in the Amazonian Craton during the Late-Paleoproterozoic. In particular, the presence of large regional-scale fissural systems and caldera collapses produced large silicic explosive volcanic eruptions, also accompanied by the emission of large volume effusive products. Although studies on the Amazonian Craton are still scarce and controversial, the present study provides new evidence that this volcanism may have formed one of the largest Silicic Large Igneous Provinces (SLIP) on earth. Our data also confirm that at least two major Paleoproterozoic periods of formation of volcanic rocks exist in the Amazonian craton. This point is of great relevance for any future interpretation of the geological evolution of this craton.
Abstract: The study of Paleoproterozoic rocks is crucial for understanding Earth's tectonic evolution during the time when most of the modern crust and ore deposits were formed. The rocks of the Brazilian Amazonian Craton record some of the most-complete and best-preserved Paleoproterozoic magmatic and volcanic episodes on Earth. Following previous investigations, we present new lithofaciological and stratigraphic records of the felsic rocks of the Tapajós Mineral Province (TMP) (~2-1.88?Ga) and the Săo Felix do Xingú region (SFX) (~1.88?Ga) which, combined with new petrological and geochronological data, help providing a more complete understanding of the tectonic, magmatic and volcanological evolution of the Amazonian Craton. This magmatism/volcanism is thought to be formed in a late-/post-orogenic to extentional regime confirmed by the new geochemical data presented here. The transition from late-convergent to extensional tectonic setting could register the beginning of the taphrogenesis that marked the Amazonian Craton throughout the Mesoproterozoic. The volcanological approach of this contribution can serve as a strategy for the modelling of the evolution of Precambrian volcano-sedimentary basins around the world. The large amount of rocks analyzed are divided into primary and secondary volcaniclastic products depending on if they resulted from a direct volcanic activity (pyroclastic) or processes that reworked pyroclastic fragments. Furthermore, the deposits are subdivided into massive and stratified, depending on their primary mechanisms of transport and emplacement. By confirming the results from previous studies, our study permits to depict a more precise paleo-environmental picture of the processes that occurred in the Amazonian Craton during the Late-Paleoproterozoic. In particular, the presence of large regional-scale fissural systems and caldera collapses produced large silicic explosive volcanic eruptions, also accompanied by the emission of large volume effusive products. Although studies on the Amazonian Craton are still scarce and controversial, the present study provides new evidence that this volcanism may have formed one of the largest Silicic Large Igneous Provinces (SLIP) on earth. Our data also confirm that at least two major Paleoproterozoic periods of formation of volcanic rocks exist in the Amazonian craton. This point is of great relevance for any future interpretation of the geological evolution of this craton.
Limiting effect of UHP metamorphism on length scales of oxygen, hydrogen and argon isotope exchange: an example from the Qinglongshan UHP eclogites, Sulu Terrain.
International Geology Review, Vol. 47, 7, pp. 716-749.
Abstract: The Cana Brava complex is the northernmost of three layered complexes outcropping in the Goiás state (central Brasil). New field and geochemical evidences suggest that Cana Brava underwent hyper- to subsolidus deformation during its growth, acquiring a high-temperature foliation that is generally interpreted as the result of a granulite-facies metamorphic event. The increase along the stratigraphy of the incompatible elements abundances (LREE, Rb, Ba) and of the Sr isotopic composition, coupled with a decrease in eNd(790), indicate that the complex was contaminated by the embedded xenoliths from the Palmeirópolis Sequence. The geochemical data suggest that the contamination occurred along the entire magma column during the crystallization of the Upper Mafic Zone, with in situ variations determined by the abundance and composition of the xenoliths. These features of the Cana Brava complex point to an extremely similarity with the Lower Sequence of the most known Niquelândia intrusion (the central of the three complexes). This, together with the evidences that the two complexes have the same age (c.a. 790 Ma) and their thickness and units decrease northwards suggests that Cana Brava and Niquelândia are part of a single giant Brasilia body grown through several melt impulses.
Gondwana Research, Vol. 70, pp. 1-24. doi:10.1016/ j.gr.2018.12.005
South America, Brazil
craton
Abstract: The study of Paleoproterozoic rocks is crucial for understanding Earth's tectonic evolution during the time when most of the modern crust and ore deposits were formed. The rocks of the Brazilian Amazonian Craton record some of the most-complete and best-preserved Paleoproterozoic magmatic and volcanic episodes on Earth. Following previous investigations, we present new lithofaciological and stratigraphic records of the felsic rocks of the Tapajós Mineral Province (TMP) (~2-1.88?Ga) and the Săo Felix do Xingú region (SFX) (~1.88?Ga) which, combined with new petrological and geochronological data, help providing a more complete understanding of the tectonic, magmatic and volcanological evolution of the Amazonian Craton. This magmatism/volcanism is thought to be formed in a late-/post-orogenic to extentional regime confirmed by the new geochemical data presented here. The transition from late-convergent to extensional tectonic setting could register the beginning of the taphrogenesis that marked the Amazonian Craton throughout the Mesoproterozoic. The volcanological approach of this contribution can serve as a strategy for the modelling of the evolution of Precambrian volcano-sedimentary basins around the world. The large amount of rocks analyzed are divided into primary and secondary volcaniclastic products depending on if they resulted from a direct volcanic activity (pyroclastic) or processes that reworked pyroclastic fragments. Furthermore, the deposits are subdivided into massive and stratified, depending on their primary mechanisms of transport and emplacement. By confirming the results from previous studies, our study permits to depict a more precise paleo-environmental picture of the processes that occurred in the Amazonian Craton during the Late-Paleoproterozoic. In particular, the presence of large regional-scale fissural systems and caldera collapses produced large silicic explosive volcanic eruptions, also accompanied by the emission of large volume effusive products. Although studies on the Amazonian Craton are still scarce and controversial, the present study provides new evidence that this volcanism may have formed one of the largest Silicic Large Igneous Provinces (SLIP) on earth. Our data also confirm that at least two major Paleoproterozoic periods of formation of volcanic rocks exist in the Amazonian craton. This point is of great relevance for any future interpretation of the geological evolution of this craton.
Journal of South American Earth Sciences, Vol. 92, pp. 197-208.
South America, Brazil
craton
Abstract: The Carajás-Rio Maria region, together with the Rio Maria domain of the Central Amazonian province, comprises the eastern margin of the Amazonian Craton with the Neoproterozoic Araguaia belt. This region hosts several basaltic dyke swarms whose UPb baddeleyite ages highlighted three intrusive events at 1882, 535 and 200?Ma. New geochemical and SrNd isotopic data were obtained for the different groups of the Carajás dykes allowing new insights on i) the mantle source composition beneath the Carajás region through time and ii) the geodynamic setting of the intrusive events. The 1882?Ma swarm is coeval to the Uatumă SLIP event which is one of the oldest intraplate events of the proto-Amazonian craton. Trace elements and isotopic values suggest that the dyke parent melt for those dykes have a crustal component derived from a sedimentary source similar to GLOSS (GLObal Subducting Sediment compositions). This is consistent with the emplacement of the dykes in a supra-subduction setting or in a post-collisional setting. Trace and isotopic values of the 535?Ma dyke swarm are consistent with an enriched mantle source from EMII component. These geochemical features suggest an enrichment of the mantle from an oceanic lithosphere poor in sediments, different to that of the 1882?Ma source. The age of this swarm matches magmatic activity during a post-collisional extensive-transtensive event recorded in the marginal Araguaia belt after the amalgamation of the Amazonian Craton to the Western Gondwana during Neoproterozoic. The 200?Ma dyke swarm which is related to the CAMP (Central Atlantic Magmatic Province) and opening of the Atlantic Ocean shows trace element composition similar to Atlantic E-MORB. The coupled isotopic values are consistent with an enriched mantle source with EMII component. These particular geochemical features suggest that the plume activity responsible for the CAMP near the rifting zone has not affected the mantle beneath the Carajás region.
Abstract: The study of Paleoproterozoic rocks is crucial for understanding Earth's tectonic evolution during the time when most of the modern crust and ore deposits were formed. The rocks of the Brazilian Amazonian Craton record some of the most-complete and best-preserved Paleoproterozoic magmatic and volcanic episodes on Earth. Following previous investigations, we present new lithofaciological and stratigraphic records of the felsic rocks of the Tapajós Mineral Province (TMP) (~2-1.88?Ga) and the Săo Felix do Xingú region (SFX) (~1.88?Ga) which, combined with new petrological and geochronological data, help providing a more complete understanding of the tectonic, magmatic and volcanological evolution of the Amazonian Craton. This magmatism/volcanism is thought to be formed in a late-/post-orogenic to extentional regime confirmed by the new geochemical data presented here. The transition from late-convergent to extensional tectonic setting could register the beginning of the taphrogenesis that marked the Amazonian Craton throughout the Mesoproterozoic. The volcanological approach of this contribution can serve as a strategy for the modelling of the evolution of Precambrian volcano-sedimentary basins around the world. The large amount of rocks analyzed are divided into primary and secondary volcaniclastic products depending on if they resulted from a direct volcanic activity (pyroclastic) or processes that reworked pyroclastic fragments. Furthermore, the deposits are subdivided into massive and stratified, depending on their primary mechanisms of transport and emplacement. By confirming the results from previous studies, our study permits to depict a more precise paleo-environmental picture of the processes that occurred in the Amazonian Craton during the Late-Paleoproterozoic. In particular, the presence of large regional-scale fissural systems and caldera collapses produced large silicic explosive volcanic eruptions, also accompanied by the emission of large volume effusive products. Although studies on the Amazonian Craton are still scarce and controversial, the present study provides new evidence that this volcanism may have formed one of the largest Silicic Large Igneous Provinces (SLIP) on earth. Our data also confirm that at least two major Paleoproterozoic periods of formation of volcanic rocks exist in the Amazonian craton. This point is of great relevance for any future interpretation of the geological evolution of this craton.
Abstract: The study of Paleoproterozoic rocks is crucial for understanding Earth's tectonic evolution during the time when most of the modern crust and ore deposits were formed. The rocks of the Brazilian Amazonian Craton record some of the most-complete and best-preserved Paleoproterozoic magmatic and volcanic episodes on Earth. Following previous investigations, we present new lithofaciological and stratigraphic records of the felsic rocks of the Tapajós Mineral Province (TMP) (~2-1.88?Ga) and the Săo Felix do Xingú region (SFX) (~1.88?Ga) which, combined with new petrological and geochronological data, help providing a more complete understanding of the tectonic, magmatic and volcanological evolution of the Amazonian Craton. This magmatism/volcanism is thought to be formed in a late-/post-orogenic to extentional regime confirmed by the new geochemical data presented here. The transition from late-convergent to extensional tectonic setting could register the beginning of the taphrogenesis that marked the Amazonian Craton throughout the Mesoproterozoic. The volcanological approach of this contribution can serve as a strategy for the modelling of the evolution of Precambrian volcano-sedimentary basins around the world. The large amount of rocks analyzed are divided into primary and secondary volcaniclastic products depending on if they resulted from a direct volcanic activity (pyroclastic) or processes that reworked pyroclastic fragments. Furthermore, the deposits are subdivided into massive and stratified, depending on their primary mechanisms of transport and emplacement. By confirming the results from previous studies, our study permits to depict a more precise paleo-environmental picture of the processes that occurred in the Amazonian Craton during the Late-Paleoproterozoic. In particular, the presence of large regional-scale fissural systems and caldera collapses produced large silicic explosive volcanic eruptions, also accompanied by the emission of large volume effusive products. Although studies on the Amazonian Craton are still scarce and controversial, the present study provides new evidence that this volcanism may have formed one of the largest Silicic Large Igneous Provinces (SLIP) on earth. Our data also confirm that at least two major Paleoproterozoic periods of formation of volcanic rocks exist in the Amazonian craton. This point is of great relevance for any future interpretation of the geological evolution of this craton.
Barry, P.H., de Moor, J.M., Giovannelli, D., Schrenk, M., Hummer, D.R., Lopez, T., Pratt, C.A., Alpizar Segua, Y., Battaglia, A., Beaudry, A., Bini, G., Cascante, M., d'Errico, G., di Carlo, M., Fattorini, D., Fullerton, K., H+Gazel, E., Gonzalez, G., Hal
Abstract: Carbon and other volatiles in the form of gases, fluids or mineral phases are transported from Earth’s surface into the mantle at convergent margins, where the oceanic crust subducts beneath the continental crust. The efficiency of this transfer has profound implications for the nature and scale of geochemical heterogeneities in Earth’s deep mantle and shallow crustal reservoirs, as well as Earth’s oxidation state. However, the proportions of volatiles released from the forearc and backarc are not well constrained compared to fluxes from the volcanic arc front. Here we use helium and carbon isotope data from deeply sourced springs along two cross-arc transects to show that about 91 per cent of carbon released from the slab and mantle beneath the Costa Rican forearc is sequestered within the crust by calcite deposition. Around an additional three per cent is incorporated into the biomass through microbial chemolithoautotrophy, whereby microbes assimilate inorganic carbon into biomass. We estimate that between 1.2 × 108 and 1.3 × 1010 moles of carbon dioxide per year are released from the slab beneath the forearc, and thus up to about 19 per cent less carbon is being transferred into Earth’s deep mantle than previously estimated.
Brovarone, A.V., Butch, C.J., Ciappa, A., Cleaves, H.J., Elmaleh, A., Faccenda, M., Feineman, M., Hermann, J., Nestola, F., Cordone, A., Giovannelli., D.
American Mineralogist, Vol. 105, pp. 1152-1160. pdf
Mantle
carbon
Abstract: Water plays a key role in shaping our planet and making life possible. Given the abundance of water on Earth's surface and in its interior, chemical reactions involving water, namely hydration and dehydration reactions, feature prominently in nature and are critical to the complex set of geochemical and biochemical reactions that make our planet unique. This paper highlights some fundamental aspects of hydration and dehydration reactions in the solid Earth, biology, and man-made materials, as well as their connections to carbon cycling on our planet.
Journal of South American Earth Sciences, Vol. 80, pp. 1-17.
South America, Brazil
carbonatite
Abstract: We present results of U-Pb dating (by MC-ICP-MS) of zircons from samples that cover all of the known lithotypes in the Seis Lagos Carbonatite Complex and associated lateritic mineralization (the Morro dos Seis Lagos Nb deposit). The host rock (gneiss) yielded an age of 1828 ± 09 Ma interpreted as the crystallization time of this unit. The altered feldspar vein in the same gneiss yielded an age of 1839 ± 29 Ma. Carbonatite samples provided 3 groups of ages. The first group comprises inherited zircons with ages compatible with the gneissic host rock: 1819 ± 10 Ma (superior intercept), 1826 ± 5 Ma (concordant age), and 1812 ± 27 Ma (superior intercept), all from the Orosirian. The second and the third group of ages are from the same carbonatite sample: the superior intercept age of 1525 ± 21 Ma (MSWD Ľ 0.77) and the superior intercept age of 1328 ± 58 Ma (MSWD Ľ 1.4). The mineralogical study indicates that the ~1.3 Ga zircons have affinity with carbonatite. It is, however, a tendence rather than a well-defined result. The data allow state that the age of 1328 ± 58 Ma represents the maximum age of the carbonatite. Without the same certainty, we consider that the data suggest that this age may be the carbonatite age, whose emplacement would have been related to the evolution of the K'Mudku belt. The best age obtained in laterite samples (a superior intercept age of 1828 ± 12 Ma) is considered the age of the main source for the inherited zircons related to the gneissic host rock.
Abstract: The Morro dos Seis Lagos niobium rare earth element, Ti-bearing lateritic deposit (Amazonas, Brazil) is derived from a primary siderite carbonatite. The complex is the only example of a Nb deposit in which Nb-rich rutile is the main Nb ore mineral. Apart from the laterites, at the current level of exposure the complex consists only of siderite carbonatite; silicate rocks are absent. Three types of siderite carbonatite are recognized: (1) a brecciated and oxidized core siderite carbonatite consisting of up to 95 vol% siderite together with: hematite; pyrochlore; Nb-brookite; Ti-maghemite; and thorobastnäsite; (2) a REE- and P-rich variety of the core siderite carbonatite consisting of siderite (up to 95 vol%), hematite, minor pyrochlore, monazite and bastnäsite; (3) a border hydrothermal siderite carbonatite with ~70 vol% siderite, barite (~15 vol%), gorceixite (~7 vol%) and minor rhabdophane and pyrochlore. The country rock gneiss in which the carbonatite was emplaced was affected by potassic fenitization, with the formation of phlogopite and orthoclase together with monazite, fluorapatite and bastnäsite. The siderite carbonatites exhibit a wide variation of d13C (-5.39‰ to -1.40‰), accompanied by a significant variation in d18O (17.13‰ to 31.33‰), especially in the REE-rich core siderite carbonatite, and are explained as due to the presence of both H2O and CO2 in the magma. The core siderite carbonatite is the richest in Fe (48.64-70.85 wt% Fe2O3) and the poorest in Ca (up 0.82 wt% CaO) example of a siderite carbonatite yet recognized The ferrocarbonatite has significant contents of Mn, Ba, Th, Pb and LREE, and a very high Nb (up to 7667 ppm) content due to the presence of Nb-brookite. The substitution 3Ti4+ = Fe2+ + 2Nb5+ recognized in Nb-rich brookite explains enrichment of Nb in the core siderite carbonatite and indicates formation in a reducing environment. The high Nb/Ta ratio (1408-11,459) of the carbonatite is compatible with residual liquids derived by fractional crystallization. The 87Sr/86Sr (0.70411-0.70573) and 144Nd/143Nd (0.512663-0.512715) isotopic data suggest the carbonatite is mantle-derived with essentially no crustal contamination and is younger than the maximum age of 1328 ± 58 Ma (UPb in zircon). We suggest that the Morro dos Seis Lagos carbonatite complex represents the upper-most parts of a differentiated carbonatite magmatic system, and that the siderite carbonatite is related to late-magmatic-to-carbo-hydrothermal processes.
Contributions to Mineralogy and Petrology, Vol. 175, 15p.
Canada
olivine
Abstract: Interactions between carbonated ultramafic silicate magmas and the continental lithospheric mantle results in the formation of dunite—a ubiquitous xenolith type in kimberlites and aillikites. However, whether this process dominantly occurs in the mantle source region or by subsequent interactions between lithospheric mantle fragments and transporting silica-undersaturated magmas during ascent remains debated. Aillikite magmas, which are derived from the fusion of carbonate-phlogopite metasomes under diamond-stability field upper mantle conditions, have a mineralogically more complex source than kimberlites, providing an opportunity to more fully constrain the origin of dunite xenoliths in such deeply sourced carbonated silicate magmas. Here we present a major and trace element study of olivine occurring in xenoliths and as phenocrysts in an aillikite dike located on the southern Superior Craton. We show that olivine within the dunite microxenoliths exhibits extreme enrichment in Al, Cr, Na, and V when compared to equivalent xenoliths carried by kimberlites. We interpret these results as evidence for the presence of carbonate-phlogopite metasomes left residual in the cratonic mantle source during aillikite magma formation. Our results are inconsistent with models of dunite formation through orthopyroxene dissolution upon kimberlite/aillikite magma ascent, supporting an origin for such dunites that is more closely linked to primary melt generation at the base of relatively thick continental lithosphere. Our work demonstrates that it is possible to constrain the precursor composition of cratonic mantle dunite at depth, thereby facilitating the further exploration of how carbonated silicate magmas modify and weaken continental lithospheric roots.
Abstract: Rheological properties of the lower mantle have strong influence on the dynamics and evolution of Earth. By using the improved methods of quantitative deformation experiments at high pressures and temperatures, we deformed a mixture of bridgmanite and magnesiowüstite under the shallow lower mantle conditions. We conducted experiments up to about 100% strain at a strain rate of about 3 × 10(-5) second(-1). We found that bridgmanite is substantially stronger than magnesiowüstite and that magnesiowüstite largely accommodates the strain. Our results suggest that strain weakening and resultant shear localization likely occur in the lower mantle. This would explain the preservation of long-lived geochemical reservoirs and the lack of seismic anisotropy in the majority of the lower mantle except the boundary layers.
Abstract: The strength of subducted slabs in the mantle transition zone influences the style of mantle convection. Intense deformation is observed particularly in relatively old subducted slabs in the deep mantle transition zone. Understanding the cause of this regional and depth variation in slab deformation requires constraint of the rheological properties of deep mantle materials. Here, we report results of in situ deformation experiments during the olivine to ringwoodite phase transformation, from which we infer the deformation process under the conditions of cold slabs deep in the mantle transition zone. We find that newly transformed fine-grained ringwoodite deforms by diffusion creep and that its strength is substantially smaller than that of coarser-grained minerals but increases with time. Scaling analysis, based on a model of transformation kinetics and grain-size evolution during a phase transformation, suggests that a cold slab will be made of a mixture of weak, fine-grained and strong, coarse-grained materials in the deep transition zone, whereas a warm slab remains strong because of its large grain size. We propose that this temperature dependence of grain size may explain extensive deformation of cold slabs in the deep transition zone but limited deformation of relatively warm slabs.
Abstract: The strength of subducted slabs in the mantle transition zone influences the style of mantle convection. Intense deformation is observed particularly in relatively old subducted slabs in the deep mantle transition zone. Understanding the cause of this regional and depth variation in slab deformation requires constraint of the rheological properties of deep mantle materials. Here, we report results of in situ deformation experiments during the olivine to ringwoodite phase transformation, from which we infer the deformation process under the conditions of cold slabs deep in the mantle transition zone. We find that newly transformed fine-grained ringwoodite deforms by diffusion creep and that its strength is substantially smaller than that of coarser-grained minerals but increases with time. Scaling analysis, based on a model of transformation kinetics and grain-size evolution during a phase transformation, suggests that a cold slab will be made of a mixture of weak, fine-grained and strong, coarse-grained materials in the deep transition zone, whereas a warm slab remains strong because of its large grain size. We propose that this temperature dependence of grain size may explain extensive deformation of cold slabs in the deep transition zone but limited deformation of relatively warm slabs.
Abstract: U-Pb baddeleyite ages for key mafic dykes of the Amazonian Craton reveal four significant intraplate episodes that allow connections with global igneous activity through time and supercontinent cycles. The oldest dykes (Carajás-Rio Maria region) are diabases with ages of 1880.2 ± 1.5 Ma and 1884.6 ± 1.6 Ma, respectively, corresponding with the Tucumă swarm which crops out to the west and is age-equivalent. The magmatic activity has a genetic link with the ca. 1.88 Ga Uatumă Silicic Large Igneous Province (SLIP), characterized by felsic plutonic-volcanic rocks. There is an age correlation with LIP events (ca. 1880 Ma) in the Superior, Slave, Indian and other cratons. This magmatism could be derived from significant perturbations of the upper mantle during the partial assembly of Columbia. Gabbronorite of the Rio Perdido Suite (Rio Apa Terrane) crystallized at 1110.7 ± 1.4 Ma, and is identical to that of the Rincón del Tigre-Huanchaca LIP event of the Amazonian Craton. This event was synchronous with the initiation of Keweenawan magmatism of central Laurentia (Midcontinent Rift) and also with coeval units in the Kalahari, Congo and India cratons. The two youngest U-Pb dates (535 and 200 Ma) occur in the Carajás region. Diabase of the Paraupebas swarm yields an age of 535.1 ± 1.1 Ma, which may be correlative with the giant Piranhas swarm located ca. 900 km apart to the west. The Paraupebas swarm is correlative with post-collisional plutonism within the Araguaia marginal belt. Therefore, the Cambrian dykes may reflect reactivation of cooled lithosphere, due to crustal extension/transtension active along the craton’s margin during assembly of West Gondwana. This magmatism is also contemporaneous with the 539-530 Ma Wichita LIP of southern Laurentia. The youngest studied Carajás region dyke was emplaced at ca. 200 Ma, corresponding with 40Ar/39Ar ages for the Periquito dykes west of Carajás and with most K-Ar ages of the giant Cassiporé swarm, located north of the study area. The newly dated ca. 200 Ma dyke fits well into the known, brief span of ages for the CAMP Large Igneous Province event, around the present central and northern Atlantic Ocean.
Abstract: The Cana Brava complex is the northernmost of three layered complexes outcropping in the Goiás state (central Brasil). New field and geochemical evidences suggest that Cana Brava underwent hyper- to subsolidus deformation during its growth, acquiring a high-temperature foliation that is generally interpreted as the result of a granulite-facies metamorphic event. The increase along the stratigraphy of the incompatible elements abundances (LREE, Rb, Ba) and of the Sr isotopic composition, coupled with a decrease in eNd(790), indicate that the complex was contaminated by the embedded xenoliths from the Palmeirópolis Sequence. The geochemical data suggest that the contamination occurred along the entire magma column during the crystallization of the Upper Mafic Zone, with in situ variations determined by the abundance and composition of the xenoliths. These features of the Cana Brava complex point to an extremely similarity with the Lower Sequence of the most known Niquelândia intrusion (the central of the three complexes). This, together with the evidences that the two complexes have the same age (c.a. 790 Ma) and their thickness and units decrease northwards suggests that Cana Brava and Niquelândia are part of a single giant Brasilia body grown through several melt impulses.
Journal of South American Earth Sciences, Vol. 92, pp. 197-208.
South America, Brazil
craton
Abstract: The Carajás-Rio Maria region, together with the Rio Maria domain of the Central Amazonian province, comprises the eastern margin of the Amazonian Craton with the Neoproterozoic Araguaia belt. This region hosts several basaltic dyke swarms whose UPb baddeleyite ages highlighted three intrusive events at 1882, 535 and 200?Ma. New geochemical and SrNd isotopic data were obtained for the different groups of the Carajás dykes allowing new insights on i) the mantle source composition beneath the Carajás region through time and ii) the geodynamic setting of the intrusive events. The 1882?Ma swarm is coeval to the Uatumă SLIP event which is one of the oldest intraplate events of the proto-Amazonian craton. Trace elements and isotopic values suggest that the dyke parent melt for those dykes have a crustal component derived from a sedimentary source similar to GLOSS (GLObal Subducting Sediment compositions). This is consistent with the emplacement of the dykes in a supra-subduction setting or in a post-collisional setting. Trace and isotopic values of the 535?Ma dyke swarm are consistent with an enriched mantle source from EMII component. These geochemical features suggest an enrichment of the mantle from an oceanic lithosphere poor in sediments, different to that of the 1882?Ma source. The age of this swarm matches magmatic activity during a post-collisional extensive-transtensive event recorded in the marginal Araguaia belt after the amalgamation of the Amazonian Craton to the Western Gondwana during Neoproterozoic. The 200?Ma dyke swarm which is related to the CAMP (Central Atlantic Magmatic Province) and opening of the Atlantic Ocean shows trace element composition similar to Atlantic E-MORB. The coupled isotopic values are consistent with an enriched mantle source with EMII component. These particular geochemical features suggest that the plume activity responsible for the CAMP near the rifting zone has not affected the mantle beneath the Carajás region.
Abstract: The subparallel maflc dykes of the Aorida-Durazno-S.José region (SW Uruguay) trend N60-80W and vary in thickness from 0.6 to 50 m. They are part of the mafic dyke swarms intrudlng granitic-gnelssic basement that were mappecl by BOSSI et ai. (1989), In an ares approximately 200 km In length and 100 km in bresdth. Plagioclass, augite, subcalclc augite (plgeonite) and opaques are the maln components of the dykes. Orthopyroxene and oIlvine are very rare. Blotite and homblende are secondary minerais. Quartz-feldspar Intergrowths occur In the coarser gralnecl dykes. The characterlstlc textures are subophitic and intersertal.
Abstract: The consumption of mineral resources and energy has increased exponentially over the last 100 years. Further growth is expected until at least the middle of the 21st century as the demand for minerals is stimulated by the industrialization of poor countries, increasing urbanization, penetration of rapidly evolving high technologies, and the transition to low-carbon energies. In order to meet this demand, more metals will have to be produced by 2050 than over the last 100 years, which raises questions about the sustainability and conditions of supply. The answers to these questions are not only a matter of available reserves. Major effort will be required to develop new approaches and dynamic models to address social, economic, environmental, geological, technological, legal and geopolitical impacts of the need for resources.
Paleoclimatic and structural environment at the end of the Cretaceous along the western flank of the Congo Basin, with application of undergroundmicrodiamonds.
Journal of African Earth Sciences, Vol. 10, No. 1/2. pp. 399-408
Proceedings Natural Science Academy, Vol. 86, 1, pp. 301-311.
India
kimberlite, lamproites
Abstract: Highlights of researches on kimberlites, lamproites and lamprophyres (and their entrained xenoliths) during 2016-2019 from the Indian context are presented. A few previously unknown occurrences have been brought to light, and a wealth of petrological, geochemical and isotopic data on these rocks became available. All these studies provided new insights into the nomenclatural as well as geodynamic aspects such as subduction-tectonics, mantle metasomatism, lithospheric thickness, supercontinent amalgamation, and break-up and nature of the sub-continental lithospheric mantle from the Indian shield.
Journal of Mineralogical and petrological Sciences, Vol. 115, 2, pp. 202-215. pdf
India
deposit - Wajrakarur
Abstract: Petrology and geochemistry (including Sr and Nd isotopes) of two lamprophyre dykes, intruding the Archaean granitic gneisses at Sivarampeta in the diamondiferous Wajrakarur kimberlite field (WKF), eastern Dharwar craton, southern India, are presented. The Sivarampeta lamprophyres display porphyritic-panidiomorphic texture comprising macrocrysts/phenocrysts of olivine, clinopyroxene (augite), and mica set in a groundmass dominated by feldspar and comprising minor amounts of ilmenite, chlorite, carbonates, epidote, and sulphides. Amphibole (actinolite-tremolite) is essentially secondary in nature and derived from the alteration of clinopyroxene. Mica is compositionally biotite and occurs as a scattered phase throughout. Mineralogy suggests that these lamprophyres belong to calc-alkaline variety whereas their bulk-rock geochemistry portrays mixed signals of both alkaline as well as calc-alkaline (shoshonitic) variety of lamprophyres and suggest their derivation from the recently identified Domain II (orogenic-anorogenic transitional type mantle source) from eastern Dharwar craton. Trace element ratios imply melt-derivation from an essentially the garnet bearing-enriched lithospheric mantle source region; this is further supported by their 87Sr/86Srinitial (0.708213 and 0.708507) and ‘enriched’ eNdinitial (-19.1 and -24.2) values. The calculated TDM ages (2.7-2.9 Ga) implies that such enrichment occurred prior to or during Neoarchean, contrary to that of the co-spatial and co-eval kimberlites which originated from an isotopically depleted mantle source which was metasomatized during Mesoproterozoic. The close association of calc-alkaline shoshonitic lamprophyres, sampling distinct mantle sources, viz., Domain I (e.g., Udiripikonda) and Domain II (Sivarampeta), and kimberlites in the WKF provide further evidence for highly heterogeneous nature of the sub-continental lithospheric mantle beneath the eastern Dharwar craton.
Abstract: Lamprophyres are some of the oldest recognized alkaline rocks and have been studied for almost the last 150 years. Known for hosting economic minerals such as gold, diamond and base metals, they are also significant in our understanding of the deep-mantle processes (viz., mantle metasomatism and mantleplume-lithosphere interactions) as well as large-scale geodynamic processes (viz., subduction-tectonics, supercontinent amalgamation and break-up). The Indian shield is a collage of distinct cratonic blocks margined by the mobile belts and manifested by large igneous provinces (LIPs) such as the Deccan. A plethora of lamprophyres, varying in age from the Archaean to the Eocene, with diverse mineralogical and geochemical compositions, are recorded from the Indian shield and played a key role in clarifying the tectonic processes, especially during the Paleo- and Mesoproterozoic and the Late Cretaceous. A comprehensive review of the occurrence, petrology, geochemistry and origin of the Indian lamprophyres is provided here highlighting their tectonomagmatic significance. The relationship of the lamprophyres to the Kimberlite clan rocks (KCRs), focusing on the Indian examples, is also critically examined.
Average compositions of magmas and mantle sources of Mid-Ocean Ridges and intraplate Oceanic and Continental settings estimated from the dat a of melt inclusions
Deep Seated Magmatism, its sources and plumes, Ed. Vladykin, N.V., p.35-78,
Average composition of basic magmas and mantle sources of island arcs and active continental margins estimated from the dat a on melt inclusions and quenched glasses
Vladykin, N.V., Deep Seated Magmatism: its sources and plumes, pp. 22-53.
Average compositions of igneous melts from main geodynamic settings according to the investigation of melt inclusions in minerals& quenched glasses of rocks.
Deep Seated Magmatism, its sources and plumes, Ed. Vladykin, N.V., pp. 171-204.
Girnis, A.V., Bulatov, V.K., Brey, G.P., Gerdes, A., Hofer, H.E.
Trace element partitioning between mantle minerals and silico-carbonate melts at 6-12 Gpa and applications to mantle metasomatism and kimberlite genesis.
Contributions to Mineralogy and Petrology, Vol. 170, 25p.
Technology
Experimental petrology
Abstract: Melting of carbonated sediment in the presence of graphite or diamond was experimentally investigated at 7.5–12 GPa and 800–1600 °C in a multianvil apparatus. Two starting materials similar to GLOSS of Plank and Langmuir (Chem Geol 145:325–394, 1998) were prepared from oxides, carbonates, hydroxides and graphite. One mixture (Na-gloss) was identical in major element composition to GLOSS, and the other was poorer in Na and richer in K (K-gloss). Both starting mixtures contained ~6 wt% CO2 and 7 wt% H2O and were doped at a ~100 ppm level with a number of trace elements, including REE, LILE and HFSE. The near-solidus mineral assemblage contained a silica polymorph (coesite or stishovite), garnet, kyanite, clinopyroxene, carbonates (aragonite and magnesite-siderite solid solution), zircon, rutile, bearthite and hydrous phases (phengite and lawsonite at <9 GPa and the hydrous aluminosilicates topaz-OH and phase egg at >10 GPa). Hydrous phases disappear at ~900 °C, and carbonates persist up to 1000-1100 °C. At temperatures >1200 °C, the mineral assemblage consists of coesite or stishovite, kyanite and garnet. Clinopyroxene stability depends strongly on the Na content in the starting mixture; it remains in the Na-gloss composition up to 1600 °C at 12 GPa, but was not observed in K-gloss experiments above 1200 °C. The composition of melt or fluid changes gradually with increasing temperature from hydrous carbonate-rich (<10 wt% SiO2) at 800-1000 °C to volatile-rich silicate liquids (up to 40 wt% SiO2) at high temperatures. Trace elements were analyzed in melts and crystalline phases by LA ICP MS. The garnet-melt and clinopyroxene-melt partition coefficients are in general consistent with results from the literature for volatile-free systems and silicocarbonate melts derived by melting carbonated peridotites. Most trace elements are strongly incompatible in kyanite and silica polymorphs (D < 0.01), except for V, Cr and Ni, which are slightly compatible in kyanite (D > 1). Aragonite and Fe-Mg carbonate have very different REE partition coefficients (D Mst-Sd/L ~ 0.01 and D Arg/L ~ 1). Nb, Ta, Zr and Hf are strongly incompatible in both carbonates. The bearthite/melt partition coefficients are very high for LREE (>10) and decrease to ~1 for HREE. All HFSE are strongly incompatible in bearthite. In contrast, Ta, Nb, Zr and Hf are moderately to strongly compatible in ZrSiO4 and TiO2 phases. Based on the obtained partition coefficients, the composition of a mobile phase derived by sediment melting in deep subduction zones was calculated. This phase is strongly enriched in incompatible elements and displays a pronounced negative Ta-Nb anomaly but no Zr-Hf anomaly. Although all experiments were conducted in the diamond stability field, only graphite was observed in low-temperature experiments. Spontaneous diamond nucleation and the complete transformation of graphite to diamond were observed at temperatures above 1200-1300 °C. We speculate that the observed character of graphite-diamond transformation is controlled by relationships between the kinetics of metastable graphite dissolution and diamond nucleation in a hydrous silicocarbonate melt that is oversaturated in C.
Abstract: Diamond nucleation and growth were investigated experimentally at 7.5 and 10.5?GPa and temperatures up to 1500?°C. Samples consisted of two layers: i) H2O- and CO2-bearing model sediment and ii) graphite-bearing garnet harzburgite comprising natural minerals. Two experimental series were conducted, one under a controlled temperature gradient with the sedimentary layer usually in the cold zone and the other under isothermal conditions. In the latter case, diamond seeds were added to the sedimentary mixture. During the experiments, the sedimentary layer partially or completely melted, with the melt percolating and interacting with the adjacent harzburgite. The graphite-to-diamond transition in the peridotite was observed above 1300?°C at 7.5?GPa and 1200?°C at 10.5?GPa in the temperature-gradient experiments, and at temperatures ~100?°C lower in the isothermal experiments with diamond seeds. Newly formed diamond occurs mostly as individual grains up to 10?µm in size and is separate from graphite aggregates. In some cases, an association of diamond with magnesite was observed. Diamond nucleation occurs in hydrous and CO2-bearing silicate melt following graphite dissolution and recrystallization. In the case of the diamond-magnesite association, diamond was probably formed through carbonate reduction coupled with graphite oxidation. The composition of the melts ranged from “carbonatitic” with ~10?wt% SiO2 and?>?50?wt% volatiles to hydrous silicate with ~40?wt% SiO2 and?
Geochemistry International, Vol. 55, 4, pp. 360-366.
Russia, Siberia
diamondoid
Abstract: A broad suite of geological materials were studied a using a handheld laser-induced breakdown spectroscopy (LIBS) instrument. Because LIBS is simultaneously sensitive to all elements, the full broadband emission spectrum recorded from a single laser shot provides a ‘chemical fingerprint’ of any material - solid, liquid or gas. The distinguishing chemical characteristics of the samples analysed were identified through principal component analysis (PCA), which demonstrates how this technique for statistical analysis can be used to identify spectral differences between similar sample types based on minor and trace constituents. Partial least squares discriminant analysis (PLSDA) was used to distinguish and classify the materials, with excellent discrimination achieved for all sample types. This study illustrates through four selected examples involving carbonate minerals and rocks, the oxide mineral pair columbite-tantalite, the silicate mineral garnet and native gold how portable, handheld LIBS analysers can be used as a tool for real-time chemical analysis under simulated field conditions for element or mineral identification plus such applications as stratigraphic correlation, provenance determination and natural resources exploration.
SIMS analyses on trace and rare earth elements in coexisting clinopyroxene and mica from minette mafic enclaves in potassic syenites crystallized under high pressure.
Contributions to Mineralogy and Petrology, Vol. 148, 6, pp. 675-688.
Journal of the Geological Society of India, Vol. 87, 6, pp. 709-715.
India
Carbonatite
Abstract: The Siriwasan carbonatite-sill along with associated alkaline rocks and fenites is located about 10 km north of the well-known Amba Dongar carbonatite-alkaline rocks diatreme, in the Chhota Udaipur carbonatite-alkaline province. Carbonatite has intruded as a sill into the Bagh sandstone and overlying Deccan basalt. This resulted in the formation of carbonatite breccia with enclosed fragments of basement metamorphics, sandstone and fenites in the matrix of ankeritic carbonatite. The most significant are the plugs of sovite with varied mineralogy that include pyroxene, amphibole, apatite, pyrochlore, perovskite and sphene. REE in sovites is related to the content of pyrochlore, perovskite and apatite. The carbon and oxygen isotopic compositions of some sovite samples and an ankeritic carbonatite plot in the "mantle box" pointing to their mantle origin. However, there is also evidence for mixing of the erupting carbonatite magma with the overlying Bagh limestone. The carbonatites of Siriwasan and Amba Dongar have the same Sr and Nd isotopic ratios and radiometric age, suggesting the same magma source. On the basis of available chemical analyses this paper is aimed to give some details of the Siriwasan carbonatites. The carbonatite complex has good potential for an economic mineral deposit but this is the most neglected carbonatite of the Chhota Udaipur province.
Abstract: The Karelian Craton in Finland is host to (at least) two distinct pulses of kimberlite magmatism. Twenty kimberlite occurrences have so far been discovered on the southwest margin of the craton at Kaavi-Kuopio and seven kimberlites are located in the Kuusamo area within the core of the craton. Comprehensive radiometric age determinations (U-Pb, Ar- Ar and Rb-Sr) reveal that all kimberlite activity was restricted to the Proterozoic. The Kaavi-Kuopio field was emplaced over a protracted period from ~610 to 550 Ma and is predated by the Kuusamo cluster that represents a relatively short pulse of magmatism at ~750 to 730 Ma. The emplacement of kimberlites globally has recently been linked to supercontinent reorganisation and we propose a similar scenario for these Finnish occurrences which, at the time of kimberlite emplacement, were situated on the Baltica paleo-continent. This land mass was contiguous with Laurentia in the Proterozoic and together formed part of Rodinia. The breakup of Rodinia is considered to have commenced at ~750 Ma and initiation of the opening of the Iapetus ocean at ~615 Ma. Contemporaneous with Kaavi-Kuopio magmatism, this latter period of Neoproterozoic crustal extension also includes the emplacement of kimberlites and related rocks in areas that were linked with Baltica as part of Rodinia - West Greenland and eastern North America. Both the initial and final periods of Rodinia’s breakup have been linked to mantle upwellings from the core-mantle boundary. We suggest that kimberlite magmatism in Finland was promoted by the influx of heat from mantle upwellings and lithospheric extension associated with the demise of Rodinia. Although both magmatic episodes are potentially linked to the breakup of Rodinia, whole-rock and perovskite radiogenic isotope compositions for the Kuusamo kimberlites (eNd(i) +2.6 to +3.3, eHf(i) +3.1 to +5.6) are distinct from the Kaavi-Kuopio kimberlites (eNd(i) -0.7 to +1.8, eHf(i) -6.1 to +5.2). The spread in Hf isotope compositions for the Kaavi-Kuopio magmas may be linked to variable assimilation of diverse mantle lithologies.
Abstract: Origin determination is of increasing importance in the gem trade. It is possible because there is a close relationship between the geological environment of formation and the physical and chemical properties of gemstones, such as trace element and isotopic compositions, that can be measured in the laboratory using combinations of increasingly sophisticated instrumentation. Origin conclusions for ruby, sapphire, and emerald make up the bulk of demand for these services, with growing demand for alexandrite, tourmaline, and spinel. However, establishing origin with a high degree of confidence using the capabilities available today is met with varying degrees of success. Geographic origin can be determined with a high level of confidence for materials such as emerald, Paraíba-type tourmaline, alexandrite, and many rubies. For some materials, especially blue sapphire and some rubies, the situation is more difficult. The main problem is that if the geology of two deposits is similar, then the properties of the gemstones they produce will also be similar, to the point where concluding an origin becomes seemingly impossible in some cases. Origin determination currently relies on a combination of traditional gemological observations and advanced analytical instrumentation.
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;
Abstract: Hypabyssal kimberlites are subvolcanic intrusive rocks crystallised from mantle-derived magmas poor in SiO2 and rich in CO2 and H2O. They are complex, hybrid rocks containing significant amounts of mantle-derived fragments, primarily olivine with rare diamonds, set in a matrix of essentially magmatic origin. Unambiguous identification of kimberlites requires careful petrographic examination combined with mineral compositional analyses. Melt inclusion studies have shown that kimberlite melts contain higher alkali concentrations than previously thought but have not clarified the ultimate origin of these melts. Because of the hybrid nature of kimberlites and their common hydrothermal alteration by fluids of controversial origin (magmatic and/or crustal), the composition of primary kimberlite melts remains unknown.
Abstract: Our discovery of moissanite grains in a peralkaline syenite from the Água de Pau Volcano (Săo Miguel, Azores Islands, Portugal) represents the first report of this mineral in present day oceanic geodynamic settings. Raman spectroscopy and single-crystal X-ray diffraction show the presence of both the 6H and 4H polytypes with the predominance of the first one. The distribution of trace elements is homogeneous, except for Al and V. Azorean moissanite often hosts rounded inclusions of metallic Si and other not yet identified metallic alloys. A process involving a flushing of CH4-H2 ultra-reducing fluids in the alkaline melts might be considered as a possible mechanism leading to the formation of natural SiC, thus calling for strongly reducing conditions that were locally met in the crust-mantle beneath the Săo Miguel Island.
Abstract: Our discovery of moissanite grains in a peralkaline syenite from the Água de Pau Volcano (Săo Miguel, Azores Islands, Portugal) represents the first report of this mineral in present day oceanic geodynamic settings. Raman spectroscopy and single-crystal X-ray diffraction show the presence of both the 6H and 4H polytypes with the predominance of the first one. The distribution of trace elements is homogeneous, except for Al and V. Azorean moissanite often hosts rounded inclusions of metallic Si and other not yet identified metallic alloys. A process involving a flushing of CH4-H2 ultra-reducing fluids in the alkaline melts might be considered as a possible mechanism leading to the formation of natural SiC, thus calling for strongly reducing conditions that were locally met in the crust-mantle beneath the Săo Miguel Island.
Journal of Petrology, 10.1093/petrology /egaa062/5857610 90p. Pdf
Africa, South Africa
deposit - Kimberley
Abstract: Olivine is the most abundant phase in kimberlites and is stable throughout most of the crystallisation sequence, thus providing an extensive record of kimberlite petrogenesis. To better constrain the composition, evolution, and source of kimberlites we present a detailed petrographic and geochemical study of olivine from multiple dyke, sill, and root zone kimberlites in the Kimberley cluster (South Africa). Olivine grains in these kimberlites are zoned, with a central core, a rim overgrowth, and occasionally an external rind. Additional ‘internal’ and ‘transitional’ zones may occur between the core and rim, and some samples of root zone kimberlites contain a late generation of high-Mg olivine in cross-cutting veins. Olivine records widespread pre-ascent (proto-)kimberlite metasomatism in the mantle including: (a) Relatively Fe-rich (Mg# <89) olivine cores interpreted to derive from the disaggregation of kimberlite-related megacrysts (20% of cores); (b) Mg-Ca-rich olivine cores (Mg# >89; >0.05?wt.% CaO) suggested to be sourced from neoblasts in sheared peridotites (25% of cores); (c) transitional zones between cores and rims probably formed by partial re-equilibration of xenocrysts (now cores) with a previous pulse of kimberlite melt (i.e., compositionally heterogeneous xenocrysts); and (d) olivine from the Wesselton water tunnel sills, internal zones (I), and low-Mg# rims, that crystallised from a kimberlite melt that underwent olivine fractionation within the shallow lithospheric mantle. Magmatic crystallisation begins with internal olivine zones (II), which are common but not ubiquitous in the Kimberley olivine. These zones are euhedral, contain rare inclusions of chromite, and have a higher Mg# (90.0 ± 0.5), NiO, and Cr2O3 contents, but are depleted in CaO compared to the rims. Internal olivine zones (II) are interpreted to crystallise from a primitive kimberlite melt during its ascent and transport of olivine toward the surface. Their compositions suggest assimilation of peridotitic material (particularly orthopyroxene) and potentially sulfides prior to or during crystallisation. Comparison of internal zones (II) with liquidus olivine from other mantle-derived carbonate-bearing magmas (i.e., orangeites, ultramafic lamprophyres, melilitites) show that low (100×) Mn/Fe (~1.2), very low Ca/Fe (~0.6), and moderate Ni/Mg ratios (~1.1) appear to be the hallmarks of olivine in melts derived from carbonate-bearing garnet-peridotite sources. Olivine rims display features indicative of magmatic crystallisation, which are typical of olivine rims in kimberlites worldwide - i.e. primary inclusions of chromite, Mg-ilmenite and rutile, homogeneous Mg# (88.8 ± 0.3), decreasing Ni and Cr, increasing Ca and Mn. Rinds and high-Mg olivine are characterised by extreme Mg-Ca-Mn enrichment and Ni depletion, and textural relationships indicate these zones represent replacement of pre-existing olivine, with some new crystallisation of rinds. These zones likely precipitated from evolved, oxidised, and relatively low-temperature kimberlite fluids after crustal emplacement. In summary, this study demonstrates the utility of combined petrography and olivine geochemistry to trace the evolution of kimberlite magmatic systems from early metasomatism of the lithospheric mantle by (proto-)kimberlite melts, to crystallisation at different depths en route to surface, and finally late-stage deuteric/hydrothermal fluid alteration processes after crustal emplacement.
Giuliani, A., Kamenetsky, V.S., Kendrick, M.A., Phillips, D., Wyatt, B.A., Maas, R.
Oxide, sulphide and carbonate minerals in a mantle polymict breccia: metasomatism by proto-kimberlite magmas, and relationship to the kimberlite megacrystic suite.
Abstract: Mantle-derived carbonatites are igneous rocks dominated by carbonate minerals. Intrusive carbonatites typically contain calcite and, less commonly, dolomite and siderite as the only carbonate minerals. In contrast, lavas erupted by the only active carbonatite volcano on Earth, Oldoinyo Lengai, Tanzania, are enriched in Na-rich carbonate phenocrysts (nyerereite and gregoryite) and Na-K halides in the groundmass. The apparent paradox between the compositions of intrusive and extrusive carbonatites has not been satisfactorily resolved. This study records the fortuitous preservation of halite in the intrusive dolomitic carbonatite of the St.-Honoré carbonatite complex (Québec, Canada), more than 490 m below the present surface. Halite occurs intergrown with, and included in, magmatic minerals typical of intrusive carbonatites; i.e., dolomite, calcite, apatite, rare earth element fluorocarbonates, pyrochlore, fluorite, and phlogopite. Halite is also a major daughter phase of melt inclusions hosted in early magmatic minerals, apatite and pyrochlore. The carbon isotope composition of dolomite (d13C = –5.2‰) and Sr-Nd isotope compositions of individual minerals (87Sr/86Sri = 0.70287 in apatite, to 0.70443 in halite; eNd = +3.2 to +4.0) indicate a mantle origin for the St.-Honoré carbonatite parental melt. More radiogenic Sr compositions of dolomite and dolomite-hosted halite and heavy oxygen isotope composition of dolomite (d18O = +23‰) suggest their formation at some time after magma emplacement by recrystallization of original magmatic components in the presence of ambient fluids. Our observations indicate that water-soluble chloride minerals, common in the modern natrocarbonatite lavas, can be significant but ephemeral components of intrusive carbonatite complexes. We therefore infer that the parental magmas that produce primary carbonatite melts might be enriched in Na and Cl. This conclusion affects existing models for mantle source compositions, melting scenarios, temperature, rheological properties, and crystallization path of carbonatite melts.
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’).
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.
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: 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).
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: 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 d18O composition of the BK bulk carbonate fraction is above the mantle range, whereas the d13C 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 d18O 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.
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 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-µ (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: 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-µ (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.
Earth and Planetary Science Letters, Vol. 401, pp. 132-147.
Africa, South Africa
metasomatism
Abstract: The Karoo igneous rocks (174-185 Ma) of southern Africa represent one of the largest continental flood basalt provinces on Earth. Available evidence indicates that Karoo magmas either originated in the asthenosphere and were extensively modified by interaction with the lithospheric mantle prior to emplacement in the upper crust; or were produced by partial melting of enriched mantle lithosphere. However, no direct evidence of interaction by Karoo melts (or their precursors) with lithospheric mantle rocks has yet been identified in the suites of mantle xenoliths sampled by post-Karoo kimberlites in southern Africa. Here we report U-Pb ages for lindsleyite-mathiasite (LIMA) titanate minerals (crichtonite series) from three metasomatised, phlogopite and clinopyroxene-rich peridotite xenoliths from the ~84 Ma Bultfontein kimberlite (Kimberley, South Africa), located in the southern part of the Karoo magmatic province. The LIMA minerals appear to have formed during metasomatism of the lithospheric mantle by fluids enriched in HFSE (Ti, Zr, Hf, Nb), LILE (K, Ba, Ca, Sr) and LREE. LIMA U-Pb elemental and isotopic compositions were measured in situ by LA-ICP-MS methods, and potential matrix effects were evaluated by solution-mode analysis of mineral separates. LIMA minerals from the three samples yielded apparent U-Pb ages of , and (). A single zircon grain extracted from the ~190 Ma LIMA-bearing sample produced a similar U-Pb age of , within uncertainty of the LIMA ages. These data provide the first robust evidence of fluid enrichment in the lithospheric mantle beneath the Kimberley region at ~180-190 Ma, and suggest causation of mantle metasomatism by Karoo melts or their precursor(s). The results further indicate that U-Pb dating of LIMA minerals provides a new, accurate tool for dating metasomatic events in the lithospheric mantle.
Earth and Planetary Science Letters, Vol. 482, pp. 253-264.
Africa, South Africa
metasomatism
Abstract: Radiogenic isotope variations unrelated to radiogenic ingrowth are common between minerals found in metasomatised mantle xenoliths entrained in kimberlite, basalts and related magmas. As the metasomatic minerals are assumed to have been in isotopic equilibrium originally, such variations are typically attributed to contamination by the magma host and/or interaction with mantle fluids during or before xenolith transport to surface. However, the increasing evidence of metasomatism by multiple, compositionally distinct fluids permeating the lithospheric mantle, coeval with specific magmatic events, suggests that isotopic disequilibrium might be a consequence of discrete, though complex, metasomatic events. Here we provide clear evidence of elemental and Sr isotope heterogeneity between coeval Ti-rich LIMA (lindsleyite–mathiasite) minerals at the time of their formation in the mantle. LIMA minerals occur in close textural association with clinopyroxene and phlogopite in low-temperature (~800–900?°C), strongly metasomatised mantle xenoliths from the ~84 Ma Bultfontein kimberlite (South Africa). Previous U/Pb dating of the LIMA phases was used to argue that each xenolith recorded a single event of LIMA crystallisation at ~180–190 Ma, coeval with the emplacement of Karoo magmas. SEM imaging reveals that up to four types of LIMA phases coexist in each xenolith, and occasionally in a single LIMA grain. Major element and in situ Sr isotope analyses of the different LIMA types show that each phase has a distinct elemental composition and initial 87Sr/86Sr ratio (e.g., 0.7068–0.7086 and 0.7115–0.7129 for two LIMA types in a single xenolith; 0.7053-0.7131 across the entire sample suite). These combined age and isotopic constraints require that multiple fluids metasomatised these rocks at broadly the same time (i.e. within a few thousands to millions of years), and produced similar mineralogical features. Elemental and isotopic variations between different LIMA types could be due to interaction between one (or more) Karoo-related Ti-rich silicate melts and previously metasomatised, phlogopite-rich lithospheric mantle. This study demonstrates that mantle metasomatic assemblages seemingly generated in a single event may instead result from the infiltration of broadly coeval fluids with variable compositions. This in turn implies that the isotopic variations recorded in mantle rocks may be an inherent feature of metasomatism, and that hot fluids infiltrating a rock do not necessarily cause equilibration at the cm scale, as has been assumed previously. Simple modelling of solid-state diffusion in mantle minerals shows that isotopic disequilibrium may be preserved for up to hundreds of Myr at mantle lithosphere temperatures (=1100–1200?°C), unless subsequently affected by transient heating and/or fluid infiltration events. Radiogenic isotope disequilibrium associated with mantle metasomatism may therefore be a common feature of mantle xenoliths.
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.
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 (d34SVCDT = +4.69 ‰) and sulfides (d34SVCDT = -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 (d13CVPDB = -9.18 ‰ d18OVSMOW = +17.22‰) are not typical of kimberlites or other mantle carbonates (d13CVPDB = -3 to -8‰ d18OVSMOW = 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.
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, 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.
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: 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.
Abstract: MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) and PIC (Phlogopite-Ilmenite-Clinopyroxene) rocks are unusual mantle samples entrained by kimberlites and other alkaline volcanic rocks. The formation of MARID rocks remains hotly debated. Although the incompatible element (for example, large ion lithophile element) enrichment in these rocks suggests that they formed by mantle metasomatism, the layered textures of some MARID samples (and MARID veins in composite xenoliths) are more indicative of formation by magmatic processes. MARID lithologies have also been implicated as an important source component in the genesis of intraplate ultramafic potassic magmas (e.g., lamproites, orangeites, ultramafic lamprophyres), due to similarities in their geochemical and isotopic signatures. To determine the origins of MARID and PIC xenoliths and to understand how they relate to alkaline magmatism, this study presents new mineral major and trace element data and bulk-rock reconstructions for 26 MARID and PIC samples from the Kimberley-Barkly West area in South Africa. Similarities between compositions of PIC minerals and corresponding phases in metasomatised mantle peridotites are indicative of PIC formation by pervasive metasomatic alteration of peridotites. MARID genesis remains a complicated issue, with no definitive evidence precluding either the magmatic or metasomatic model. MARID minerals exhibit broad ranges in Mg# (e.g., clinopyroxene Mg# from 82 to 91), which may be indicative of fractionation processes occurring in the MARID-forming fluid/melt. Finally, two quantitative modelling approaches were used to determine the compositions of theoretical melts in equilibrium with MARID rocks. Both models indicate that MARID-derived melts have trace element patterns resembling mantle-derived potassic magma compositions (e.g., lamproites, orangeites, ultramafic lamprophyres), supporting inferences that these magmas may originate from MARID-rich mantle sources.
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.
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; eNdi: +3.0 to +3.6; eHfi: +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; eNdi: -11.0 to -1.0; eHfi: -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 (?eHfi 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; eNdi = -11.0; eHfi = -17.9; and 206Pb/204Pbi = 17.3) by the entraining kimberlite magma (87Sr/86Sr; eNd; eHf; 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 ?eHfi values in kimberlites. The isotopic composition of the inferred initial MARID end-member, with high 87Sr/86Sr and low eNd, eHf, 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.
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 d15N and d18O 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 d18O values of olivine and orthopyroxene in phlogopite-free harzburgites match the mantle composition (d18Oolivine?=?+5.2?±?0.3‰; d18Oorthopyroxene?=?+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 d18O values, the d15N value of phlogopite in a wehrlite sample (+5.9‰) differs from the mantle composition (d15N?=?-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 d18O values (as low as +4.4‰) extend below those reported in mantle peridotites (i.e. d18Oclinopyroxene?=?+5.6?±?0.3‰; 2?s.d.), and strong negative correlations are found between mineral d18O values and major element compositions (e.g., Na2O contents in clinopyroxene). Furthermore, phlogopite d15N values (+4 to +7‰) in the studied lherzolite and MARID samples are higher than mantle values. Combined, the low d18O-high d15N 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.
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 d18O 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 d18O and Mn-Ca concentrations, with d18O 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 d18O 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 d18O 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.
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 th
