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SDLRC - Scientific Articles all years by Author - Ko-Kq
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
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Physics of the Earth and Planetary Interiors, Vol. 305, 13p. Pdf
Mantle
density
Abstract: The composition of Archean volcanic crust can be characterized by a higher Mg/Si ratio than modern mid-ocean ridge basalt (MORB), because of the higher degree melting from the warmer mantle in the Archean. Although modern MORB may become less dense than the surrounding mantle beneath the mantle transition zone (MTZ), the Mg-rich composition of Archean volcanic crust may result in the different density, and therefore different sinking behavior near the MTZ. In order to understand the compositional effect of Archean volcanic crust on the sinking behaviors and the scale of mantle mixing in the Archean, we investigated the mineralogy and density of Archean volcanic crust near the MTZ (470-910 km-depth). We conducted experiments at 19-34 GPa and 1400-2400 K using the laser-heated diamond anvil cell (LHDAC) combined with in-situ X-ray diffraction (XRD). The in-situ XRD and the chemical analysis revealed that Archean volcanic crust forms garnet and ringwoodite (84 and 16 vol%, respectively), which gradually transforms to Brg and CaPv (82 and 18 vol%, respectively) at 23-25 GPa and 1800 K. Our in-situ XRD experiments allowed us to measure the volumes of stable phases and to estimate their densities at high pressure and temperature. The results suggest that Archean volcanic crust maintains greater density than the pyrolitic mantle in the Archean regardless of temperature at 20-34 GPa (570-850 km-depth), promoting further sinking into the deeper mantle in the Archean. We also considered the density of the subducting slab in the Archean. The density model showed that the subducting slab is still denser or at least equally dense as the surrounding pyrolitic mantle in the Archean.
Physics of the Earth and Planetary Interiors, Vol. 305, 13p. Pdf
Mantle
subduction
Abstract: The composition of Archean volcanic crust can be characterized by a higher Mg/Si ratio than modern mid-ocean ridge basalt (MORB), because of the higher degree melting from the warmer mantle in the Archean. Although modern MORB may become less dense than the surrounding mantle beneath the mantle transition zone (MTZ), the Mg-rich composition of Archean volcanic crust may result in the different density, and therefore different sinking behavior near the MTZ. In order to understand the compositional effect of Archean volcanic crust on the sinking behaviors and the scale of mantle mixing in the Archean, we investigated the mineralogy and density of Archean volcanic crust near the MTZ (470-910 km-depth). We conducted experiments at 19-34 GPa and 1400-2400 K using the laser-heated diamond anvil cell (LHDAC) combined with in-situ X-ray diffraction (XRD). The in-situ XRD and the chemical analysis revealed that Archean volcanic crust forms garnet and ringwoodite (84 and 16 vol%, respectively), which gradually transforms to Brg and CaPv (82 and 18 vol%, respectively) at 23-25 GPa and 1800 K. Our in-situ XRD experiments allowed us to measure the volumes of stable phases and to estimate their densities at high pressure and temperature. The results suggest that Archean volcanic crust maintains greater density than the pyrolitic mantle in the Archean regardless of temperature at 20-34 GPa (570-850 km-depth), promoting further sinking into the deeper mantle in the Archean. We also considered the density of the subducting slab in the Archean. The density model showed that the subducting slab is still denser or at least equally dense as the surrounding pyrolitic mantle in the Archean.
Manya, S., Kobayashi, K., Maboko, M.A., Nakamura, E.
Ion microprobe zircon U Pb dating of the late Archean metavolcanics and associated granites of the Musoma Mara greenstone belt, northeast Tanzania: implications
Journal of African Earth Sciences, Vol. 45, 3, pp. 355-366.
Tang, Y-J., Zhang, H-F., Nakamura, E., Moriguti, T., Kobayashi, K., Ying, J-F.
Lithium isotopic systematics of peridotite xenoliths from Hannuoba, North Chin a Craton: implications for melt rock interaction in considerably thinned mantle lithospheric mantle.
Geochimica et Cosmochimica Acta, Vol. 71, 17, Sept. 1, pp. 4327-4341.
Zhang, H-F., Nakamura, E., Sun, M., Kobayashi,K., Zhang, J., Yang, J-F., Tang, Y-J.
Transformation of subcontinental lithospheric mantle through peridotite melt reaction: evidence from a highly fertile mantle xenolith from the North Chin a Craton.
International Geology Review, Vol. 49, 7, July pp. 658-679.
Earth and Planetary Science Letters, Vol. 483, 1, pp. 90-104.
Europe, Iceland
olivines
Abstract: Trace element variability in oceanic basalts is commonly used to constrain the physics of mantle melting and the chemistry of Earth's deep interior. However, the geochemical properties of mantle melts are often overprinted by mixing and crystallisation processes during ascent and storage. Studying primitive melt inclusions offers one solution to this problem, but the fidelity of the melt-inclusion archive to bulk magma chemistry has been repeatedly questioned. To provide a novel check of the melt inclusion record, we present new major and trace element analyses from olivine macrocrysts in the products of two geographically proximal, yet compositionally distinct, primitive eruptions from the Reykjanes Peninsula of Iceland. By combining these macrocryst analyses with new and published melt inclusion analyses we demonstrate that olivines have similar patterns of incompatible trace element (ITE) variability to the inclusions they host, capturing chemical systematics on intra- and inter-eruption scales. ITE variability (element concentrations, ratios, variances and variance ratios) in olivines from the ITE-enriched Stapafell eruption is best accounted for by olivine-dominated fractional crystallisation. In contrast, ITE variability in olivines and inclusions from the ITE-depleted Háleyjabunga eruption cannot be explained by crystallisation alone, and must have originated in the mantle. Compatible trace element (CTE) variability is best described by crystallisation processes in both eruptions. Modest correlations between host and inclusion ITE contents in samples from Háleyjabunga suggest that melt inclusions can be faithful archives of melting and magmatic processes. It also indicates that degrees of ITE enrichment can be estimated from olivines directly when melt inclusion and matrix glass records of geochemical variability are poor or absent. Inter-eruption differences in olivine ITE systematics between Stapafell and Háleyjabunga mirror differences in melt inclusion suites, and confirm that the Stapafell eruption was fed by lower degree melts from greater depths within the melting region than the Háleyjabunga eruption. Although olivine macrocrysts from Stapafell are slightly richer in Ni than those from Háleyjabunga, their overall CTE systematics (e.g., Ni/(Mg/Fe), Fe/Mn and Zn/Fe) are inconsistent with being derived from olivine-free pyroxenites. However, the major element systematics of Icelandic basalts require lithological heterogeneity in their mantle source in the form of Fe-rich and hence fusible domains. We thus conclude that enriched heterogeneities in the Icelandic mantle are composed of modally enriched, yet nonetheless olivine-bearing, lithologies and that olivine CTE contents provide an incomplete record of lithological heterogeneity in the mantle. Modally enriched peridotites may therefore play a more important role in oceanic magma genesis than previously inferred.
Geochemistry, Geophysics, Geosystems, Vol. 20, 2, pp. 952-973.
United States, New Mexico
xenoliths
Abstract: Elemental and isotopic compositions of volatile species such as halogens, noble gases, hydrogen, and carbon can be used to trace the evolution of these species in the Earth. Halogens are important tracers of subduction recycling of surface volatiles into the mantle: however, there is only limited understanding of halogens in the mantle. Here we provide new halogen data of mantle xenoliths from intraplate settings. The mantle xenoliths show a wide range of halogen elemental ratios, which are expected to be related to later processes after the xenoliths formed. A similar primary halogen component is present in the xenoliths sampled from different localities. This suggests that the mantle has the uniform halogen composition over a wide scale. The halogen composition in the convecting mantle is expected to have remained constant over more than 2 billion years, despite subduction of iodine?rich halogens. We used mass balance calculations to gain understanding into evolution rate of I/Cl ratio in the mantle. Calculations suggest that, in order to maintain the I/Cl ratio of the mantle over 2 Gyr, the I/Cl ratio of the subducted halogens must be no more than several times higher than the present?day mantle value.
Earth and Planetary Science Letters, Vol. 558, 115763, 6p. Pdf
Europe, Italy
UHP
Abstract: The stabilization of coesite is a diagnostic indicator of ultrahigh-pressure metamorphism and in many cases it implies that a rock has been subducted to a minimum depth of 80 km. Coesite typically occurs as rare relicts in rigid host minerals, but most commonly transforms into ?-quartz pseudomorphs during exhumation. The abundance of coesite-bearing rocks in orogens worldwide is a contentious issue in the petrological community, despite evidence from numerical modeling that suggests that coesite formation should be a common geological process during ultrahigh-pressure metamorphism. This knowledge gap must be addressed to improve the understanding of the geological aspects of subduction-zone geodynamics. Here we report that minuscule coesites (<20 ?m) occur as abundant inclusions in garnet-rich layers from the Italian Western Alps. The discovery of such intact inclusions may fill the gaps in the predicted and observed abundances of coesite worldwide. Through integrated approaches with resolutions down to the nano-scale, we show that these garnet-hosted inclusions are composed entirely of coesite. Our results suggest that common coesite-derived quartz pseudomorphs are less typical structures in ultrahigh-pressure metamorphic rocks and the minuscule coesite in many rocks may be overlooked because of its size. These findings open up new research directions for constraining the extent of deeply subducted rocks and their rheology.
Provenance and reconnaissance study of detrital zircons of the Paleozoic Cape Supergroup: revealing the interaction of Kalahari and Rio de la Plat a cratons.
International Journal of Earth Sciences, Vol. 100, 2, pp. 527-541.
Mineralogical composition and geographical distribution of African and Brazilian periatlantic laterites. the influence of continental drift and tropical paleoclimes
Journal of Sth. African Earth Sciences, Vol. pp. 283-295
Abstract: Based on the mineral inclusion content, diamonds from the Argyle Mine, Western Australia, derive primarily (~90%) from eclogitic sources with a minor peridotitic contribution from both harzburgitic and lherzolitic lithologies. The eclogitic inclusions cover a large compositional range and show in part unusually high concentrations of mantle incompatible elements (P, Ti, Na and K). Coherent trends in major elements (e.g., of Ti or Na versus Mg-number) suggest that the eclogitic diamond source was created by a single process, namely igneous fractionation. Calculated bulk rock REEN patterns match a section of oceanic crust reaching from lavas and sheeted dykes to upper gabbros. Positive Eu anomalies for garnet and clinopyroxene, with calculated bulk rock REEN patterns similar to upper (non-layered) gabbros, are strong evidence for plagioclase accumulation, which is characteristic for the gabbroic portions of oceanic crust. Linking previously published oxygen isotope analyses of eclogitic garnet inclusions with their major element composition reveals a correlation between ?18O (mean of +7.2‰) and Na content, consistent with coupled 18O and Na enrichment during low temperature alteration of oceanic crust. The carbon isotopic composition of Argyle eclogitic diamonds forms a normal distribution around a ?13C value of -11‰, indicative of mixing and homogenization of mantle and crustal (organic matter) derived carbon prior to diamond precipitation. Previously published noble gas data on Argyle diamonds support this two component model. Inclusion and nitrogen-in-diamond based thermometry indicate an unusually hot origin of the eclogitic diamond suite, indicative of derivation from the lowermost 25 km (about 180-205 km depth) of the local lithospheric mantle. This is consistent with emplacement of an oceanic protolith during subduction along the Kimberley Craton margin, likely during the Halls Creek Orogeny (about 1.85 Ga). For Argyle eclogitic diamonds the relationship between the rate of platelet degradation and mantle residence temperature indicates that both temperature and strain play an important role in this process. Therefore, ubiquitous platelet degradation and plastic deformation of Argyle diamonds are consistent with derivation from a high temperature environment (softening the diamond lattice) close to the lithosphere-asthenosphere boundary (inducing strain). In combination, the Argyle data set represents a uniquely strong case for a subduction origin of an eclogitic diamond source followed by mixing of mantle and crustal components during diamond formation. Some lherzolitic inclusions show a similarity in incompatible element enrichments (elevated P, Na and K) to the eclogitic suite. The presence of a mildly majoritic lherzolitic garnet further supports a link to eclogitic diamond formation, as very similar majoritic components were found in two eclogitic garnet inclusions. The carbon isotopic composition of peridotitic diamonds shows a mode between -5 to -4 ‰ and a tail extending towards the eclogitic mode (-11 ‰). This suggests the presence of multiple generations of peridotitic diamonds, with indications for an origin linked to the eclogitic suite being restricted to diamonds of lherzolitic paragenesis.
Argyle diamonds – how subduction along the Kimberley Craton edge generated the world's biggest diamond deposit.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0630-7 14p.
Canada, Northwest Territories
deposit - Diavik
Abstract: The Diavik Diamond Mine in the NWT of Canada has produced in excess of 100 million carats from 3 kimberlite pipes since mining commenced in 2002. Here, we present new findings from deep (>400 m below surface) mining, sampling and drilling work in the A154N kimberlite volcano that require a revision of previous geological and emplacement models and provide a window into how the sub-continental lithospheric mantle (SCLM) below Diavik was sampled by kimberlite magmas through time. Updated internal geological models feature two volcanic packages interpreted to represent two successive cycles of explosive eruption followed by active and passive sedimentation from a presumed crater-rim, both preceded and followed by intrusions of coherent kimberlite. Contact relationships apparent among the geological units allow for a sequential organization of as many as five temporally-discrete emplacement events. Representative populations of mantle minerals extracted from geological units corresponding to four of the emplacement events at A154N are analyzed for major and trace elements, and provide insights into the whether or not kimberlites randomly sample from the mantle. Two independent geothermometers using clinopyroxene and garnet data indicate similar source depths for clinopyroxenes and G9 garnets (130-160 km), and suggest deeper sampling with time for both clinopyroxene and garnets. Harzburgite is limited to 110-160 km, and appears more prevalent in early, low-volume events. Variable ratios of garnet parageneses from the same depth horizons suggest random sampling by passing magmas, but deeper garnet sampling through time suggests early preferential sampling of shallow/depleted SCLM. Evaluations of Ti, Zr, Y and Ga over the range of estimated depths support models of the SCLM underlying the central Slave terrane.
Griffin, W.L., Kobussen, A.F., Babu, E.V.S.S.K., O'Reilly, S.Y., Norris, R., Sengupta, P.
A translithospheric suture in the vanished 1 Ga lithospheric root of South India: evidence from contrasting lithospheric sections in the Dharwar Craton.
Griffin, W.L., Kobussen, A.F., Babu, E.V.S.S.K., O'Reilly, S.Y., Norris, R., Sengupta, P.
A translithospheric suture in the vanished 1 Ga lithospheric root of South India: evidence from contrasting lithosphere sections in the Dharwar craton.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 201-222.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 119-144.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 223-236.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 403-424.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 237-252.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 145-168.
Abstract: The high amount of Fe-rich ferropericlase inclusions found in diamonds of a potential super-deep origin questions the bulk chemical model of the Earth [e.g., 1]. Although this might be due to a biased sampling of the lower mantle, it is worth to further address this discrepancy. A limiting factor of the Fe-content of the Earth´s deep mantle (TZ and lower mantle) is a correlation of the depths of the observed main mantle discontinuities with the (Fe,Mg)SiO4 phase diagram. In particular, the 520 kmdiscontinuity is related to the phase transformation of wadsleyite (assuming Fa10) to ringwoodite. The existing phase diagrams suggest a stability limit of wadsleyite ?Fa40 [e.g., 2,3], which limits the Fe-content of the Earth´s transition zone. Here we report on a discovery of Fe-rich wadsleyite grains (up to Fa56) in the high-pressure silicate melt droplets within Fe,Ni-metal in shock veins of the CB (Bencubbin-like) metal-rich carbonaceous chondrite QC 001 [4], which were identified using HR-EDX, nano-EBSD and TEM. Although the existence of such Fe-rich wadsleyite in shock veins may be due to the kinetic reasons, new theoretical and experimental studies of the stability of (Fe,Mg)SiO4 at high temperature (> 1800 K) are clearly needed. This may have significant impact on the temperature and chemical estimates of the Earth´s transition zone.
Abstract: Two Neoproterozoic carbonatite suites of spatially related carbonatites and associated silicate alkaline rocks from Sevattur and Samalpatti, south India, have been investigated in terms of petrography, chemistry and radiogenic–stable isotopic compositions in order to provide further constraints on their genesis. The cumulative evidence indicates that the Sevattur suite is derived from an enriched mantle source without significant post-emplacement modifications through crustal contamination and hydrothermal overprint. The stable (C, O) isotopic compositions confirm mantle origin of Sevattur carbonatites with only a modest difference to Paleoproterozoic Hogenakal carbonatite, emplaced in the same tectonic setting. On the contrary, multiple processes have shaped the petrography, chemistry and isotopic systematics of the Samalpatti suite. These include pre-emplacement interaction with the ambient crustal materials with more pronounced signatures of such a process in silicocarbonatites. Calc-silicate marbles present in the Samalpatti area could represent a possible evolved end member due to the inability of common silicate rocks (pyroxenites, granites, diorites) to comply with radiogenic isotopic constraints. In addition, Samalpatti carbonatites show a range of C–O isotopic compositions, and ?13CV-PDB values between + 1.8 and + 4.1‰ found for a sub-suite of Samalpatti carbonatites belong to the highest values ever reported for magmatic carbonates. These heavy C–O isotopic signatures in Samalpatti carbonatites could be indicative of massive hydrothermal interaction with carbonated fluids. Unusual high-Cr silicocarbonatites, discovered at Samalpatti, seek their origin in the reaction of pyroxenites with enriched mantle-derived alkali-CO2-rich melts, as also evidenced by mantle-like O isotopic compositions. Field and petrographic observations as well as isotopic constraints must, however, be combined with the complex chemistry of incompatible trace elements as indicated from their non-uniform systematics in carbonatites and their individual fractions. We emphasise that, beside common carriers of REE like apatite, other phases may be important for incompatible element budgets, such as mckelveyite–(Nd) and kosmochlor, found in these carbonatites. Future targeted studies, including in-situ techniques, could help further constrain temporal and petrologic conditions of formation of Sevattur and Samalpatti carbonatite bodies.
Ackerman, L., Magna, T., Rapprich, V., Upadhyay, D., Kratky, O., Cejkova, B., Erban, V., Kochergina, Y.V., Hrstka, T.
Contrasting petrogenesis of spatially related carbonatites from Samalpatti and Sevattur, Tamil Nadu, India: insights from trace element and isotopic geochemistry.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 31-33.
India
deposit - Samalpatti, Sevattur
Abstract: The Tamil Nadu region in southern India hosts several carbonatite bodies (e.g., Hogenakal, Samalpatti, Sevattur, Pakkanadu-Mulakkadu) which are closely associated with alkaline silicate rocks such as syenites, pyroxenites or dunites (e.g, Kumar et al., 1998; Schleicher et al., 1998; Srivastava, 1998). This is in contrast to the carbonatite occurrences in north-western India associated with the Deccan Trap basalts (e.g., Amba Dongar) or Proterozoic Newania dolomitic carbonatites. We have studied two, spatially related, Neoproterozoic carbonatite-silico(carbonatite) suites in association with alkaline silicate rocks (e.g., pyroxenite, gabbro) from Sevattur and Samalpatti in terms of petrography, chemistry and radiogenic-stable isotopic compositions in order to provide constraints on their genesis and evolution. In these two bodies, several different carbonatite types have been reported previously with striking differences in their trace element and isotopic compositions (Srivastava, 1998; Viladkar and Subramanian, 1995; Schleicher et al., 1998; Pandit et al., 2002). Collected data for previously poorly studied calcite carbonatites from the Sevattur representing the first carbonatite magmas on this locality, indicate similar geochemical characteristics to those of dolomitic carbonatites, such as high LREE/HREE ratios, very high Sr and Ba contents, large amounts of apatite and magnetite, identical Sr-Nd-C-O isotopic compositions. Thus, they were derived from an enriched mantle source without significant post-emplacement modifications through crustal contamination and hydrothermal overprint, in agreement with previous studies (e.g., Schleicher et al., 1998). Detailed microprobe analyses revealed that high levels of some incompatible elements (e.g., REE, Y, Sr, Ba) cannot be accounted by matrix calcite hosting only significant amounts of SrO (~0.6-1.2 wt.%). On the other hand, abundant micro- to nano-scale exsolution lamellae and/or inclusions of mckelveyite-(Nd) appear to host a significant fraction of LREE in parallel with apatite. Distribution of Sr is most likely influenced also by common but heterogeneously dispersed barite and strontianite. Newly acquired as well as detailed inspection of available geochemical data permits distinguish two different types of carbonatites in Samalpatti: (1) Type I similar to Sevattur carbonatites in terms of mineralogy, trace element and radiogenic-stable isotopic compositions and (2) Type II with remarkably low concentrations of REE and other incompatible trace elements, more radiogenic Sr isotopic compositions and extremely variable C–O isotopic values. The petrogenesis of the Type II seems to be intimately associated with the presence of silicocarbonatites and abundant silicate mineral domains. Instead of liquid immiscible separation from a silicate magma, elevated SiO2 contents observed in silico-carbonatites may have resulted from the interaction of primary carbonatitic melts and crustal rocks prior to and/or during magma emplacement. Arguments for such hypothesis include variable, but radiogenic Sr isotopic compositions correlated with SiO2 and other lithophile elements (e.g., Ti, Y, Zr, REE). Calc-silicate marbles present in the Samalpatti area could represent a possible evolved crustal end member for such process due to the inability of common silicate rocks (pyroxenites, granites, diorites) to comply with radiogenic isotopic constraints. The wide range of C-O isotopic compositions found in Samalpatti carbonatites belong to the highest values ever reported for magmatic carbonates and can be best explained by massive hydrothermal interaction with carbonated fluids. Unusual high-Cr silicocarbonatites were discovered at Samalpatti forming centimetre to decimetre-sized enclaves enclosed in pyroxenites with sharp contacts at hand specimen scale. Detailed microprobe analyses revealed peculiar chemical compositions of the Mgamphibole with predominantly sodic composition embaying and replacing Na-Cr-rich pyroxene (kosmochlor), accompanied by the common presence of Cr-spinel and titanite. Such association have been reported for hydrous metasomatism by Na-rich carbonatitic melts at upper mantle conditions (Ali and Arai, 2013). However, the mineralogy and the mode of occurrence of Samalpatti Mg–-r-rich silicocarbonatites argue against such origin. We explain the petrogenesis of these rocks through the reaction of pyroxenites with enriched mantle-derived alkali-CO2-rich melts, as also evidenced by mantle-like O and Hf isotopic compositions.
South African Journal of Geology, Vol. 120, 3, pp. 371-384.
Africa, Zimbabwe, South Africa
diamond morphology
Abstract: The morphological, chemical impurities and carbon isotope properties of diamonds may reveal subtle details of their mantle source and growth characteristics, supporting efforts towards identifying their original place of harvesting. Here we investigate the mantle carbon and nitrogen sources and growth patterns from selected diamonds mined from four kimberlites: macro-sized diamonds from River Ranch kimberlite in Zimbabwe and the Swartruggens and Klipspringer kimberlitic deposits from South Africa, and micro-sized diamonds from the Klipspringer and Premier kimberlite intrusions in South Africa. Type IaAB diamonds are found in all the samples; Type IaB diamonds only occur in samples from the Swartruggens, River Ranch and Premier kimberlites. A single Type II diamond (nitrogen below the detection limit) was also observed in the River Ranch and Premier kimberlites. Both the micro- and macro-sized diamonds from Klipspringer have similar nitrogen contents. Based on the % B-defect, the diamonds from Klipspringer are grouped into low- and high-nitrogen aggregates (i.e. % of B-defect <40% and >56%, respectively) that likely represent two different diamond forming episodes. Time averaged mantle storage temperatures for Type IaAB diamonds are calculated to have been: 1060°C for Swartruggens; 1190°C for River Ranch; 1100°C (low aggregated); and 1170°C (highly aggregated) for Klipspringer, and 1210°C for Premier diamonds. The CL-images of the River Ranch, Klipspringer and Premier diamonds reveal multi-oscillatory growth zones. The carbon isotopic analyses on the diamonds reveal an average ?13CVPDB value of: -4.5‰ for Swartruggens; -4.7‰ for River Ranch; -4.5‰ for Klipspringer; and -3‰ for Premier. With the exception of the diamond from Premier, the average ?13C value of the diamonds are similar to the average ?13C value of the mantle (-5‰), which is similar to the occurrence of diamonds in the other kimberlites. The internal carbon isotopic variation of individual diamonds from Swartruggens, Klipspringer and Premier are less than 4‰, which is similar to the variability of most other diamond occurrences reported from elsewhere in the world. Up to 6.7‰ internal carbon isotopic variation was observed in a single diamond from River Ranch. The internal carbon isotopic studies of the diamonds reveal that the primary carbon in the Swartruggens and Klipspringer was derived from an oxidation of CH4-bearing fluid, whereas in the River Ranch the primary carbon was derived from the reduction of carbonate-or CO2-bearing fluids. The Swartruggens diamonds also reveal a secondary carbon sourced from a reduction of CO2- or carbonate-rich fluid or melt. Diamonds from Klipspringer exhibit a cyclic change in ?13C values that reflects fluctuation in a complex mantle perturbation system or periodic change in fugacity of the mantle. Based on this study, we conclude that, in principle, a selected range of diamond signatures might be used to fingerprint their origins; especially when linked to their other physical properties such as a low temperature magnetic signature.
Earth and Planetary Science Letters, Vol. 498, pp. 9-16.
Mantle
water
Abstract: Ringwoodite, the dominant mineral at depths between 520 km and 660 km, can store up to 2-3 wt.% of water in its crystal structure, making the Earth's transition zone a plausible water reservoir that plays a central role in Earth's deep water cycle. Experiments show that hydration of ringwoodite significantly reduces elastic wave velocities at room pressure, but the effect of pressure remains poorly constrained. Here, a novel experimental setup enables a direct quantification of the effect of hydration on ringwoodite single-crystal elasticity and density at pressures of the Earth's transition zone and high temperatures. Our data show that the hydration-induced reduction of seismic velocities almost vanishes at conditions of the transition zone. Seismic data thus agree with a wide range of water contents in the transition zone.
Contributions to Mineralogy and Petrology, Vol. 174, 4, doi.org/10. 1007/s00410-018-1530-x 13p.
Mantle
carbonatite
Abstract: Here we present an experimental study of the distribution of a broad range of trace elements between carbonatite melt, calcite and fluorite. The experiments were performed in the CaCO3 + CaF2 + Na2CO3 ± Ca3(PO4)2 synthetic system at 650-900 °C and 100 MPa using rapid-quench cold-seal pressure vessels. Starting mixtures were composed of reagent-grade oxides, carbonates, Ca3(PO4)2 and CaF2 doped with 1 wt% REE-HFSE mixture. The results show that the distribution coefficients of all the analyzed trace elements for calcite and fluorite are below 1, with the highest values observed for Sr (0.48-0.8 for calcite and 0.14-0.3 for fluorite) and Y (0.18-0.3). The partition coefficients of REE gradually increase with increasing atomic number from La to Lu. The solubility of Zr, Hf, Nb and Ta in the synthetic F-rich carbonatitic melts, which were used in our experiments, is low and limited by crystallization of baddeleyite and Nb-bearing perovskite.
Palaeomagnetism of Granitic Intrusives from the Precambrian basement Under Eastern Kansas; Orienting Drill Cores Using Secondary Magnetization components.
Geophysical Journal of the Royal Astronomical Society, Vol. 76, No. 2, PP. 273-287.
Geochemistry: Exploration, Environment, Analysis, Vol. 19, pp. 414-430.
Canada, British Columbia
geochemistry
Abstract: Using Rock Canyon Creek REE-F-Ba deposit as an example, we demonstrate the need for verifying inherited geochemical data. Inherited La, Ce, Nd, and Sm data obtained by pressed pellet XRF, and La and Y data obtained by aqua regia digestion ICP-AES for 300 drill-core samples analysed in 2009 were compared to sample subsets reanalysed using lithium metaborate-tetraborate (LMB) fusion ICP-MS, Na2O2 fusion ICP-MS, and LMB fusion-XRF. We determine that LMB ICP-MS and Na2O2 ICP-MS accurately determined REE concentrations in SY-2 and SY-4, and provided precision within 10%. Fusion-XRF was precise for La and Nd at concentrations exceeding ten times the lower detection limit; however, accuracy was not established because REE concentrations in SY-4 were below the lower detection limit. Analysis of the sample subset revealed substantial discrepancies for Ce concentrations determined by pressed pellet XRF in comparison to other methods due to Ba interference. Samarium, present in lower concentrations than other REE compared, was underestimated by XRF methods relative to ICP-MS methods. This may be due to Sm concentrations approaching the lower detection limits of XRF methods, elemental interference, or inadequate background corrections. Aqua regia dissolution ICP-AES results, reporting for La and Y, are underestimated relative to other methods.
Guzmics, T., Zajacz, Z., Kodoenyi, J., Halter, W., Szabo, C.
LA ICP MS study of apatite and K feldspar hosted primary carbonatite melt inclusions in clinopyroxenite xenoliths from lamprophyres, Hungary: implications
Geochimica et Cosmochimica Acta, Vol. 72, 7, pp. 1864-1886.
Abstract: The Samchampi (26° 13?N: 93° 18?E)-Samteran (26° 11?N: 93° 25?E) alkaline complex (SSAC) occurs as an intrusion within Precambrian basement gneisses in the Karbi-Anglong district of Assam, Northeastern India. This intrusive complex comprises a wide spectrum of lithologies including syenite, ijolite-melteigite, alkali pyroxenite, alkali gabbro, nepheline syenite and carbonatite (nepheline syenites and carbonatites are later intrusives). In this paper, we present new major, trace, REE and Sr-Nd isotope data for different lithologies of SSAC and discuss integrated petrological and whole rock geochemical observations with Sr-Nd isotope systematics to understand the petrogenetic evolution of the complex. Pronounced LILE and LREE enrichment of the alkaline-carbonatite rocks together with steep LREE/HREE profile and flat HREE-chondrite normalized patterns provide evidence for parent magma generation from low degree partial melting of a metasomatized garnet peridotite mantle source. LILE, HFSE and LREE enrichments of the alkaline-silicate rocks and carbonatites are in agreement with the involvement of a mantle plume in their genesis. Nb-Th-La systematics with incompatible trace element abundance patterns marked by positive Nb-Ta anomalies and negative K, Th and Sr anomalies suggest contribution from plume-derived OIB-type mantle with recycled subduction component and a rift-controlled, intraplate tectonic setting for alkaline-carbonatite magmatism giving rise to the SSAC. This observation is corroborated by enriched 87Sr/86Srinitial (0.705562 to 0.709416) and 143Nd/144Ndinitial (0.512187 to 0.512449) ratios for the alkaline-carbonatite rocks that attest to a plume-related enriched mantle (~ EM II) source in relation to the origin of Samchampi-Samteran alkaline complex. Trace element chemistry and variations in isotopic data invoke periodic melting of an isotopically heterogeneous, metasomatized mantle and generation of isotopically distinct melt batches that were parental to the different rocks of SSAC. Various extents of plume-lithosphere interaction also accounts for the trace element and isotopic variations of SSAC. The Srinitial and Ndinitial (105 Ma) isotopic compositions (corresponding to ?Nd values of ? 6.37 to ? 1.27) of SSAC are consistent with those of Sung Valley, Jasra, Rajmahal tholeiites (Group II), Sylhet Traps and Kerguelen plateau basalts.
Koehm, D., Lindenfeld, M., Rumpker, G., Aanyu, K., Haines, S., Passchier, C.W., Sachu, T.
Active transgression faults in rift transfer zones: evidence for complex stress fields and implications for crustal fragmentation processes in the western branch
International Journal of Earth Sciences, Vol. 99, 7, pp. 1633-1642.
Earth and Planetary Science Letters, Vol. 494, pp. 226-238.
Mantle
perovskite
Abstract: Lower mantle tomography models consistently feature an increase in the ratio of shear-wave velocity () to compressional-wave velocity () variations and a negative correlation between shear-wave and bulk-sound velocity () variations. These seismic characteristics, also observed in the recent SP12RTS model, have been interpreted to be indicative of large-scale chemical variations. Other explanations, such as the lower mantle post-perovskite (pPv) phase, which would not require chemical heterogeneity, have been explored less. Constraining the origin of these seismic features is important, as geodynamic simulations predict a fundamentally different style of mantle convection under both scenarios. Here, we investigate to what extent the presence of pPv explains the observed high ratios and negative - correlation globally. We compare the statistical properties of SP12RTS with the statistics of synthetic tomography models, derived from both thermal and thermochemical models of 3-D global mantle convection. We convert the temperature fields of these models into seismic velocity structures using mineral physics lookup tables with and without pPv. We account for the limited tomographic resolution of SP12RTS using its resolution operator for both and structures. This allows for direct comparisons of the resulting velocity ratios and correlations. Although the tomographic filtering significantly affects the synthetic tomography images, we demonstrate that the effect of pPv remains evident in the ratios and correlations of seismic velocities. We find that lateral variations in the presence of pPv have a dominant influence on the / ratio and - correlation, which are thus unsuitable measures to constrain the presence of large-scale chemical variations in the lowermost mantle. To explain the decrease in the / ratio of SP12RTS close to the CMB, our results favour a pPv-bearing CMB region, which has implications for the stability field of pPv in the Earth's mantle.
Progress in Earth and Planetary Science , Vol. 7, 16p. Pdf
Mantle
geophysics - seismics
Abstract: Mantle tomography reveals the existence of two large low-shear-velocity provinces (LLSVPs) at the base of the mantle. We examine here the hypothesis that they are piles of oceanic crust that have steadily accumulated and warmed over billions of years. We use existing global geodynamic models in which dense oceanic crust forms at divergent plate boundaries and subducts at convergent ones. The model suite covers the predicted density range for oceanic crust over lower mantle conditions. To meaningfully compare our geodynamic models to tomographic structures, we convert them into models of seismic wavespeed and explicitly account for the limited resolving power of tomography. Our results demonstrate that long-term recycling of dense oceanic crust naturally leads to the formation of thermochemical piles with seismic characteristics similar to the LLSVPs. The extent to which oceanic crust contributes to the LLSVPs depends upon its density in the lower mantle for which accurate data is lacking. We find that the LLSVPs are not composed solely of oceanic crust. Rather, they are basalt rich at their base (bottom 100-200 km) and grade into peridotite toward their sides and top with the strength of their seismic signature arising from the dominant role of temperature. We conclude that recycling of oceanic crust, if sufficiently dense, has a strong influence on the thermal and chemical evolution of Earth’s mantle.
Abstract: The Earth’s mantle is characterized by a sharp seismic discontinuity at a depth of 660?km that can provide insights into deep mantle processes. The discontinuity occurs over only 2?km—or a pressure difference of 0.1?GPa—and is thought to result from the post-spinel transition, that is, the decomposition of the mineral ringwoodite to bridgmanite plus ferropericlase. Existing high-pressure, high-temperature experiments have lacked the pressure control required to test whether such sharpness is the result of isochemical phase relations or chemically distinct upper and lower mantle domains. Here, we obtain the isothermal pressure interval of the Mg-Fe binary post-spinel transition by applying advanced multi-anvil techniques with in situ X-ray diffraction with the help of Mg-Fe partition experiments. It is demonstrated that the interval at mantle compositions and temperatures is only 0.01?GPa, corresponding to 250?m. This interval is indistinguishable from zero at seismic frequencies. These results can explain the discontinuity sharpness and provide new support for whole-mantle convection in a chemically homogeneous mantle. The present work suggests that distribution of adiabatic vertical flows between the upper and lower mantles can be mapped on the basis of discontinuity sharpness.
Abstract: Majoritic garnet has been predicted to be a major component of peridotite and eclogite in Earth's deep upper mantle (>250 km) and transition zone. The investigation of mineral inclusions in diamond confirms this prediction, but there is reported evidence of other majorite-bearing lithologies, intermediate between peridotitic and eclogitic, present in the mantle transition zone. If these lithologies are derived from olivine-free pyroxenites, then at mantle transition zone pressures majorite may form monomineralic or almost monomineralic garnetite layers. Since majoritic garnet is presumably the seismically fastest major phase in the lowermost upper mantle, the existence of such majorite layers might produce a detectable seismic signature. However, a test of this hypothesis is hampered by the absence of sound wave velocity measurements of majoritic garnets with relevant chemical compositions, since previous measurements have been mostly limited to synthetic majorite samples with relatively simple compositions. In an attempt to evaluate the seismic signature of a pyroxenitic garnet layer, we measured the sound wave velocities of three natural majoritic garnet inclusions in diamond by Brillouin spectroscopy at ambient conditions. The chosen natural garnets derive from depths between 220 and 470 km and are plausible candidates to have formed at the interface between peridotite and carbonated eclogite. They contain elevated amounts (12-30%) of ferric iron, possibly produced during redox reactions that form diamond from carbonate. Based on our data, we model the velocity and seismic impedance contrasts between a possible pyroxenitic garnet layer and the surrounding peridotitic mantle. For a mineral assemblage that would be stable at a depth of 350 km, the median formation depth of our samples, we found velocities in pyroxenite at ambient conditions to be higher by 1.9(6)% for shear waves and 3.3(5)% for compressional waves compared to peridotite (numbers in parentheses refer to uncertainties in the last given digit), and by 1.3(13)% for shear waves and 2.4(10)% for compressional waves compared to eclogite. As a result of increased density in the pyroxenitic layer, expected seismic impedance contrasts across the interface between the monomineralic majorite layer and the adjacent rocks are about 5-6% at the majorite-eclogite-interface and 10-12% at the majoriteperidotite-boundary. Given a large enough thickness of the garnetite layer, velocity and impedance differences of this magnitude could become seismologically detectable.
Journal of South American Earth Sciences, Vol. 94, 102208 13p. Pdf
South America, Brazil
carbonatite
Abstract: Carbonatites are peculiar igneous rocks, consisting mainly of greater than 50% carbonate minerals, which arouse an economic interest due to the potentiality of high phosphate content and Light Rare Earth Elements (LREE) associated with their occurrence. The Passo Feio Carbonatite (PFC) is located 17?km Southwest of Caçapava do Sul city and constitutes NW dipping body, which is interposed with Passo Feio Formation metamorphic rocks. The PFC varies texturally from massive to foliated, being mainly composed of calcites and dolomites and on a smaller scale by apatites, phlogopites and tremolites. The opaque minerals correspond to hematites, magnetites, pyrites and barites, while the accessory minerals are represented by zircons, monazites- (Ce) and aeschynites- (Ce). Probably those REE mineral phases correspond to a hydrothermal stage, with the REE remobilization from apatites into those latter REE-rich mineral phases - this hypothesis is corroborated by geochemistry, mineral chemistry and microtextures found. Considering the results of mineral chemistry and taking into account the textural criteria, it was possible to classify carbonatite as an alvikite, with geochemical patterns that do not indicate economic potential for REE. However, soil geochemistry showed an important enrichment in REE, reflecting a probable concentration of monazites- (Ce) and aeschynites- (Ce), and because of this, it was possible to establish a zone in which the Passo Feio Carbonatite would probably be extended. In the stable isotope analyzes, the ?13C values varied between ?4.14 and ?3.89‰ while those of ?18O between 10.01 and 11.32‰ which can be attributed to the cooling of the magma itself, without suggesting metamorphic processes or subsequent changes. The deformation found in this carbonatite was probably developed in late-magmatic conditions, guided by tectonics associated with horizontal movements in shear zones. Thus, this work suggests that this carbonatite was the product of the reactivation of mantle sources, within a post-collision magmatic context of the Sul-Riograndense Shield.
Martin, A.M., Laporte, D., Koga, K.T., Kawamoto, T., Hammouda, T.
Experimental study of the stability of a dolomite + coesite assemblage in contact with peridotite: implications for sediment-mantle interaction and diamond formation during subduction.
Martin, A.M., Laporte, D., Koga, K.T., Kawamoto, T., Hammouda, T.
Experimental stidy of the stability of a dolomite + coesite assembalge in contact with peridotite: implications for sediment-mantle interaction and diamond formation during subduction.
Garnet pyroxene equilibration temperatures in the system CaO MgO Al2O3 SiO2(CMAS)prospects for simplified T-independent lherzolite barometry and an eclogitebarometer
Contributions to Mineralogy and Petrology, Vol. 92, No. 4, pp. 448-455
Alkaline and carbonatitic magmatism of the earth and related ore deposits.International Geological Correlation Programme (IGCP)Proposal Project 314. 1991-1995
Geochemistry International, Vol. 56, 8, pp. 766-783.
Russia, Siberia
carbonatite
Abstract: In this study we present a fresh isotopic data, as well as U-Pb ages from different REE-minerals in carbonatites and phoscorites of Guli massif using in situ LA-ICPMS technique. The analyses were conducted on apatites and perovskites from calcio-carbonatite and phoscorite units, as well as on pyrochlores and baddeleyites from the carbonatites. The 87Sr/86Sr ratios obtained from apatites and perovskites from the phoscorites are 0.70308-0.70314 and 0.70306-0.70313, respectively; and 0.70310-0.70325 and 0.70314-0.70327, for the pyrochlores and apatites from the carbonatites, respectively. Furthermore, the in situ laser ablation analyses of apatites and perovskites from the phoscorite yield ?Nd from 3.6 (±1) to 5.1 (±0.5) and from 3.8 (±0.5) to 4.9 (±0.5), respectively; ?Nd of apatites, perovskites and pyrochlores from carbonatite ranges from 3.2 (±0.7) to 4.9 (±0.9), 3.9 (±0.6) to 4.5 (±0.8) and 3.2 (±0.4) to 4.4 (±0.8), respectively. Laser ablation analyses of baddeleyites yielded an eHf(t)d of +8.5 (± 0.18); prior to this study Hf isotopic characteristic of Guli massif was not known. Our new in situ ?Nd, 87Sr/86Sr and eHf data on minerals in the Guli carbonatites imply a depleted source with a long time integrated high Lu/Hf, Sm/Nd, Sr/Rb ratios. In situ U-Pb age determination was performed on perovskites from the carbonatites and phoscorites and also on pyrochlores and baddeleyites from carbonatites. The co-existing pyrochlores, perovskites and baddeleyites in carbonatites yielded ages of 252.3 ± 1.9, 252.5 ± 1.5 and 250.8 ± 1.4 Ma, respectively. The perovskites from the phoscorites yielded an age of 253.8 ± 1.9 Ma. The obtained age for Guli carbonatites and phoscorites lies within the range of ages previously reported for the Siberian Flood Basalts and suggest essentially synchronous emplacement with the Permian-Triassic boundary.
Abstract: Three models of geodynamic regimes of carbonatite formation are now actively being developed because of the high trace metal potential of this rock type: carbonatite melt generation within the lithosphere mantle; carbonatite relation to orogenic zones; the formation of carbonatite complexes as a result of the ascent of deep mantle plumes. The application for the first time of a modern model of “absolute” paleotectonic reconstructions combined with databases (both our own and published) demonstrates the general relationship of occurrences of the Phanerozoic carbonatite magmatism to Large Low S-wave Velocity Provinces: those are allocated in the lower mantle and are zones of generation of deep mantle plumes.
Geochemistry International, Vol. 59, pp. 92-98. pdf
Russia
REE
Abstract: This paper reports the results of the first study of pyroxenes from the deepest zones of the Lovozero deposit. The geochemical and mineralogical study of these rocks is of great scientific interest, as they are the least differentiated rocks and provide insight into the composition of a parental magma. According to microprobe analysis, clinopyroxenes evolve from early diopside-hedenbergite-augite to later alkaline aegirine-augite species. Upsection, the contents of Na, Fe3+ and Ti increase, while Mg, Ca, Fe2+, and Zr decrease. Thus, isomorphic substitution in pyroxenes of the lower zone follows the scheme (Ca, Mg, Fe2+, Zr) ? (Na, Fe3+, Ti).
A Hawaiian beginning for the Iceland plume: modelling of reconnaissance dat a for olivine hosted melt inclusions in Palaeogene picrite lavas East Greenland.
Thermodynamic analysis of magnetite + titanite + clinopyroxene equilibration temperatures in apatite bearing intrusion of the Khibin a alkaline complex.
Physicochemical conditions of magma formation at the base of the Siberian plume: insights from the investigation of melt inclusions in the meymechites and alkali picrites of the Maimecha Kotui
Doklady Earth Sciences, Vol. 466, 2, Feb. pp. 135-137.
Russia
Carbonatite
Abstract: The first data on variations of the isotope composition and element ratios of carbon, nitrogen, and argon in carbonatites of different generations and ultrabasic rocks of the Guli massif obtained by the method of step crushing are reported. It is shown that early carbonatite differs significantly from the later ones by the concentration of highly volatile components, as well as by the isotope compositions of carbon (CO2), argon, and hydrogen (H2O). The data obtained allow us to conclude that the mantle component predominated in the fluid at the early stages of formation of rocks of the Guli massif, whereas the late stages of carbonatite formation were characterized by an additional fluid source, which introduced atmospheric argon, and most likely a high portion of carbon dioxide with isotopically heavy carbon.
Abstract: Zirconium and hafnium are valuable strategic metals which are in high demand in industry. The Zr and Hf contents are elevated in the final products of magmatic differentiation of alkali carbonatite rocks in the Polar Siberia region (Guli Complex) and Ukraine (Chernigov Massif). Early pyroxene fractionation led to an increase in the Zr/Hf ratio in the evolution of the ultramafic–alkali magmatic system due to a higher distribution coefficient of Hf in pyroxene with respect to Zr. The Rayleigh equation was used to calculate a quantitative model of variation in the Zr/Hf ratio in the development of the Guli magmatic system. Alkali carbonatite rocks originated from rare element-rich mantle reservoirs, in particular, the metasomatized mantle. Carbonated mantle xenoliths are characterized by a high Zr/Hf ratio due to clinopyroxene development during metasomatic replacement of orthopyroxene by carbonate fluid melt.
Contributions to Mineralogy and Petrology, Vol. 172, 32p.
Russia, Kola Peninsula
Carbonatite
Abstract: The Lovozero alkaline massif—an agpaitic nepheline syenite layered intrusion—is located in the central part of the Kola Peninsula, Russia, and belongs to the Kola ultramafic alkaline and carbonatitic province (KACP) of Devonian age. Associated loparite and eudialyte deposits, which contain immense resources of REE, Nb, Ta, and Zr, constitute a world class mineral district. Previous Sr, Nd, and Hf isotope investigations demonstrated that these rocks and mineral deposits were derived from a depleted mantle source. However, because the Sr, Nd, and Hf abundances in the Kola alkaline rocks are significantly elevated, their isotopic compositions were relatively insensitive to contamination by the underlying crustal rocks through which the intruding magmas passed. Pb occurring in relatively lower abundance in the KACP rocks, by contrast, would have been a more sensitive indicator of an acquired crustal component. Here, we investigate the lead isotopic signature of representative types of Lovozero rocks in order to further characterize their sources. The measured Pb isotopic composition was corrected using the determined U and Th concentrations to the age of the crystallization of the intrusion (376?±?28 Ma, based on a 206Pb/204Pb versus 238U/204Pb isochron and 373?±?9 Ma, from a 208Pb/204Pb versus 232Th/204Pb isochron). Unlike the previously investigated Sr, Nd, and Hf isotopes, the lead isotopic composition plot was well outside the FOZO field. The 206Pb/204Pb values fall within the depleted MORB field, with some rocks having lower 207Pb/204Pb but higher 208Pb/204Pb values. Together with other related carbonatites having both lower and higher 206Pb/204Pb values, the combined KACP rocks form an extended linear array defining either a?~2.5-Ga secondary isochron or a mixing line. The projection of this isotopic array toward the very unradiogenic composition of underlying 2.4-2.5-Ga basaltic rocks of the Matachewan superplume and associated Archean granulite facies country rock provides strong evidence that this old lower crust was the contaminant responsible for the deviation of the Lovozero rocks from a presumed original FOZO lead isotopic composition. Evaluating the presence of such a lower crustal component in the Lovozero rock samples suggests a 5-10% contamination by such rocks. Contamination by upper crustal rock is limited to only a negligible amount.
Geochemistry International, Vol. 55, 5, pp. 457-464.
Russia
carbonatite - Guli
Abstract: For better understanding of the fluid phase sources of carbonatites of Guli alkaline-ultrabasic intrusion (Maymecha-Kotuy complex) we have studied isotope composition of He and Ne in the carbonatites of different formation stages. The data definitely point to the subcontinental lithospheric mantle (SCLM) as a primary source of fluid phase of Guli carbonatites. The absence of plume signature in such a plume-like object (from petrological point of view) could be explained in terms that Guli carbonatites have been formed at the waning stage of plume magmatic activity with an essential input of SCLM components.
Abstract: Geodynamic origin of carbonatites is debated for several decades. One of hypotheses links their origin to large-volume mantle plumes rising from the core-mantle boundary (CMB). Some evidence exists for temporal and spatial relationships between the occurrences of carbonatites and large igneous provinces (LIPs), and both carbonatites and LIPs can be related to mantle plumes. A good example is the carbonatites of the Maymecha-Kotuy Province in the Polar Siberia, which were formed at the same time as the Siberian superplume event at ca. 250 Ma. In this study we use a recently published absolute plate kinematic modelling to reconstruct the position of 155 Phanerozoic carbonatites at the time of their emplacement. We demonstrate that 69% of carbonatites may be projected onto the central or peripheral parts of the large low shear-wave velocity provinces (LLSVPs) in the lowermost mantle. This correlation provides a strong evidence for the link between the carbonatite genesis and the locations of deep-mantle plumes. A large group of carbonatites (31%) has no obvious links to LLSVPs and, on the contrary, they plot above the "faster-than-average S-wave" zones in the deep mantle, currently located beneath North and Central America and China. We propose that their origin may be associated with remnants of subducted slabs in the mantle.
Abstract: Detailed studies have shown that a change in the eudialyte occurrence forms (and the moment of its crystallization) is a new geochemical criterion for rare metal ore content in alkalic magmas (eudialyte ores). A new principle of the presence of ores in alkalic magmas has been formulated: a prerequisite for the formation of an ore deposit is early saturation of alkalic magmas with an ore mineral. If the ore component concentration is significantly lower than the cotectic (saturation), then melt saturation and crystallization of an ore mineral will take place at later stages of rock formation in a small volume of the interstitial melt, when the phenomena of convective?gravity differentiation and segregation of mineral phases in the form of ore deposits are hampered. This leads to dispersion of the ore components in the form of xenomorphic grains of accessory minerals. Rocks of the differentiated complex (lower zone of the Lovozero deposit) and rocks of the Khibiny massif contain xenomorphic eudialyte and are not promising for eudialyte ores. Eudialyte deposits are associated with the upper zone of the Lovozero intrusion where euhedral early eudialyte occurs. The initial magma is saturated with eudialyte after crystallization of about 80% of the intrusion. The proposed criterion is applicable to the largest alkalic massifs in the world. The Ilimaussaq massif (Greenland), the rocks of which contain early crystallized, euhedral eudialyte, hosts a superlarge eudialyte ore deposit. Unlike the Khibiny massif and the Pilanesberg alkalic complex, the rocks of which contain late xenomorphic eudialyte, this massif has no deposits of this type.
Abstract: Geodynamic origin of carbonatites is debated for several decades. One of hypotheses links their origin to large-volume mantle plumes rising from the core-mantle boundary (CMB). Some evidence exists for temporal and spatial relationships between the occurrences of carbonatites and large igneous provinces (LIPs), and both carbonatites and LIPs can be related to mantle plumes. A good example is the carbonatites of the Maymecha-Kotuy Province in the Polar Siberia, which were formed at the same time as the Siberian superplume event at ca. 250 Ma. In this study we use a recently published absolute plate kinematic modelling to reconstruct the position of 155 Phanerozoic carbonatites at the time of their emplacement. We demonstrate that 69% of carbonatites may be projected onto the central or peripheral parts of the large low shear-wave velocity provinces (LLSVPs) in the lowermost mantle. This correlation provides a strong evidence for the link between the carbonatite genesis and the locations of deep-mantle plumes. A large group of carbonatites (31%) has no obvious links to LLSVPs and, on the contrary, they plot above the "faster-than-average S-wave" zones in the deep mantle, currently located beneath North and Central America and China. We propose that their origin may be associated with remnants of subducted slabs in the mantle.
Geochemistry International, Vol. 57, 11, pp. 1125-1146.
Russia, Siberia
carbonatite
Abstract: We report the first combined investigation (neutron activation, X-ray fluorescence, and electron microprobe analysis) of mineral forms of Au and Ag and noble metal distribution in the sulfide-bearing phoscorites and carbonatites of the Guli alkaline ultrabasic massif (Polar Siberia) and magnetite and sulfide separates from these rocks. The highest noble metal contents were observed in the sulfide separates from the carbonatites: up to 2.93 Pt, 61.6 Au, and 3.61 ppm Ag. Pyrrhotite, djerfisherite, chalcopyrite, and pyrite are the most abundant sulfides and the main hosts for Au and Ag. The latest assemblage of chalcopyrite, Ag-rich djerfisherite, lenaite, sternbergite, and native silver shows significant Ag concentrations. The wide occurrence of K sulfides and presence of multiphase inclusions in pyrrhotite consisting of rasvumite, K?Na–Ca carbonate, carbocernaite, strontianite, galena, chalcopyrite, sternbergite, lenaite, and native silver suggest that the sulfides were formed at high activities of K, Na, Sr, LREE, F, Cl, and S. Chlorine shows high complex-forming capacity to Ag and could be an agent of noble metal transport in the carbonatites. Crystallization of the early djerfisherite–pyrrhotite assemblages of the phoscorites and carbonatites began at a temperature not lower than 500°C and continued up to the formation of late Ag-bearing sulfides at temperatures not higher than 150°C. The carbonatite-series rocks could be enriched in Au and Ag during late low-temperature stages and serve as a source for Au placers.
Abstract: The Lovozero complex, Kola peninsula, Russia and the Ilímaussaq complex in Southwest Greenland are the largest known layered peralkaline intrusive complexes. Both host world-class deposits rich in REE and other high-tech elements. Both complexes expose spectacular layering with horizons rich in eudialyte group minerals (EGM). We present a detailed study of the composition and cryptic variations in cumulus EGM from Lovozero and a comparison with EGM from Ilímaussaq to further our understanding of peralkaline magma chambers processes. The geochemical signatures of Lovozero and Ilímaussaq EGM are distinct. In Lovozero EGMs are clearly enriched in Na + K, Mn, Ti, Sr and poorer Fe compared to EGM from Ilímaussaq, whereas the contents of ?REE + Y and Cl are comparable. Ilímaussaq EGMs are depleted in Sr and Eu, which points to plagioclase fractionation and an olivine basaltic parent. The absence of negative Sr and Eu anomalies suggest a melanephelinitic parent for Lovozero. In Lovozero the cumulus EGMs shows decrease in Fe/Mn, Ti, Nb, Sr, Ba and all HREE up the magmatic layering, while REE + Y and Cl contents increase. In Lovozero EGM spectra show only a weak enrichment in LREE relative to HREE. The data demonstrates a systematic stratigraphic variation in major and trace elements compositions of liquidus EGM in the Eudialyte Complex, the latest and uppermost part of Lovozero. The distribution of elements follows a broadly linear trend. Despite intersample variations, the absence of abrupt changes in the trends suggests continuous crystallization and accumulation in the magma chamber. The crystallization was controlled by elemental distribution between EGM and coexisting melt during gravitational accumulation of crystals and/or mushes in a closed system. A different pattern is noted in the Ilimaussaq Complex. The elemental trends have variable steepness up the magmatic succession especially in the uppermost zones of the Complex. The differences between the two complexes are suggested to be related dynamics of the crystallization and accumulation processes in the magma chambers, such as arrival of new liquidus phases and redistributions by mush melts
Abstract: The distribution patterns of rare earth metals (REM) in the rocks of the Kugda massif (Polar Siberia) are assessed. The REM content decreases from early olivinite rocks, containing, on average, 1938 ppm, to the end products of syenite differentiation and increases again in carbonatites. The difference in the distribution coefficients of light and heavy rare earth metals is the reason for the noticeable fractionation of these elements during the evolution of the magmatic system of the Kugda massif. The ratio of light REM to heavy Ce/Yb drops by almost an order of magnitude in later differentiation products. The main process of the Kugda massif formation was continuous crystallization differentiation, characterized by a wide crystallization field of perovskite. An interesting feature of the process is the very early crystallization of perovskite, associated with the high potential of carbon dioxide.
Plume related mantle source of super large rare metal deposits from the Lovozero and Khibin a massifs on the Kola Peninsula, east Baltic Shield: Sr, Nd, Hf isotope ssytematics.
Progress in Earth and Planetary Science, Vol. 3, 25, Aug. 22
Mantle
Experimental petrology
Abstract: The Accessible Silicate Earth (ASE) has a higher 142Nd/144Nd ratio than most chondrites. Thus, if the Earth is assumed to have formed from these chondrites, a complement low-142Nd/144Nd reservoir is needed. Such a low-142Nd/144Nd reservoir is believed to have been derived from a melt in the early Earth and is called the Early Enriched Reservoir (EER). Although the major element composition of the EER is crucial for estimating its chemical and physical properties (e.g., density) and is also essential for understanding the origin and fate of the EER, which are both major factors that determine the present composition of the Earth, it has not yet been robustly established. In order to determine the major element composition of the EER, we estimated the age and pressure-temperature conditions to form the EER that would best explain its Nd isotopic characteristics, based on Sm-Nd partitioning and its dependence on pressure, temperature, and melting phase relations. Our estimate indicates that the EER formed within 33.5 Myr of Solar System formation and at near-solidus temperatures and shallow upper-mantle pressures. We then performed high-pressure melting experiments on primitive peridotite to determine the major element composition of the EER at estimated temperature at 7 GPa and calculated the density of the EER. The result of our experiments indicates that the near-solidus melt is iron-rich komatiite. The estimated density of the near-solidus melt is lower than that of the primitive peridotite, suggesting that the EER melt would have ascended in the mantle to form an early crust. Given that high mantle potential temperatures are assumed to have existed in the Hadean, it follows that the EER melt was generated at high pressure and, therefore, its composition would have been picritic to komatiitic. As the formation age of the EER estimated in our study precedes the last giant, lunar-forming impact, the picritic to komatiitic crust (EER) would most likely have been ejected from the Earth by the last giant impact or preceding impacts. Thus, the EER has been lost, leaving the Earth more depleted than its original composition.
Geochemistry, Geophysics, Geosystems, Vol. 20, 2, pp. 952-973.
United States, New Mexico
xenoliths
Abstract: Elemental and isotopic compositions of volatile species such as halogens, noble gases, hydrogen, and carbon can be used to trace the evolution of these species in the Earth. Halogens are important tracers of subduction recycling of surface volatiles into the mantle: however, there is only limited understanding of halogens in the mantle. Here we provide new halogen data of mantle xenoliths from intraplate settings. The mantle xenoliths show a wide range of halogen elemental ratios, which are expected to be related to later processes after the xenoliths formed. A similar primary halogen component is present in the xenoliths sampled from different localities. This suggests that the mantle has the uniform halogen composition over a wide scale. The halogen composition in the convecting mantle is expected to have remained constant over more than 2 billion years, despite subduction of iodine?rich halogens. We used mass balance calculations to gain understanding into evolution rate of I/Cl ratio in the mantle. Calculations suggest that, in order to maintain the I/Cl ratio of the mantle over 2 Gyr, the I/Cl ratio of the subducted halogens must be no more than several times higher than the present?day mantle value.
Abstract: Earth and the Moon are shown here to have indistinguishable oxygen isotope ratios, with a difference in ??17O of ?1 ± 5 parts per million (2 standard error). On the basis of these data and our new planet formation simulations that include a realistic model for primordial oxygen isotopic reservoirs, our results favor vigorous mixing during the giant impact and therefore a high-energy, high-angular-momentum impact. The results indicate that the late veneer impactors had an average ??17O within approximately 1 per mil of the terrestrial value, limiting possible sources for this late addition of mass to the Earth-Moon system.
Abstract: Nitrogen is the main constituent of the Earth’s atmosphere, but its provenance in the Earth’s mantle remains uncertain. The relative contribution of primordial nitrogen inherited during the Earth’s accretion versus that subducted from the Earth’s surface is unclear1,2,3,4,5,6. Here we show that the mantle may have retained remnants of such primordial nitrogen. We use the rare 15N15N isotopologue of N2 as a new tracer of air contamination in volcanic gas effusions. By constraining air contamination in gases from Iceland, Eifel (Germany) and Yellowstone (USA), we derive estimates of mantle ?15N (the fractional difference in 15N/14N from air), N2/36Ar and N2/3He. Our results show that negative ?15N values observed in gases, previously regarded as indicating a mantle origin for nitrogen7,8,9,10, in fact represent dominantly air-derived N2 that experienced 15N/14N fractionation in hydrothermal systems. Using two-component mixing models to correct for this effect, the 15N15N data allow extrapolations that characterize mantle endmember ?15N, N2/36Ar and N2/3He values. We show that the Eifel region has slightly increased ?15N and N2/36Ar values relative to estimates for the convective mantle provided by mid-ocean-ridge basalts11, consistent with subducted nitrogen being added to the mantle source. In contrast, we find that whereas the Yellowstone plume has ?15N values substantially greater than that of the convective mantle, resembling surface components12,13,14,15, its N2/36Ar and N2/3He ratios are indistinguishable from those of the convective mantle. This observation raises the possibility that the plume hosts a primordial component. We provide a test of the subduction hypothesis with a two-box model, describing the evolution of mantle and surface nitrogen through geological time. We show that the effect of subduction on the deep nitrogen cycle may be less important than has been suggested by previous investigations. We propose instead that high mid-ocean-ridge basalt and plume ?15N values may both be dominantly primordial features.
Kohler, J., Schonenberger, J., Upton, B., Markl, G.
Halogen and trace element chemistry in the Gardar Province, South Greenland: subduction related mantle metasomatism and fluid exsolution from alkalic melts.
Geostandards and Geoanalysis Research, doi.org/10.1111/GGR.12419 34p. Pdf
Australia
geochemistry
Abstract: To promote a more efficient and transparent geochemistry data ecosystem, a consortium of Australian university research laboratories called the AuScope Geochemistry Network (AGN) assembled to build a collaborative platform for the express purpose of preserving, disseminating, and collating geochronology and isotopic data. In partnership with geoscience-data-solutions company Lithodat Pty Ltd, the open, cloud-based AusGeochem platform (https://ausgeochem.auscope.org.au) was developed to simultaneously serve as a geosample registry, a geochemical data repository, and a data analysis tool. Informed by method-specific groups of geochemistry experts and established international data reporting practices, community-agreed database schemas were developed for rock and mineral geosample metadata and secondary ion mass spectrometry U-Pb analysis, with additional models for laser ablation inductively-coupled mass spectrometry U-Pb and Lu-Hf, Ar-Ar, fission-track and (U-Th-Sm)/He under development. Collectively, the AusGeochem platform provides the geochemistry community with a new, dynamic resource to help facilitate FAIR (Findable, Accessible, Interoperable, Reusable) data management, streamline data dissemination and advanced quantitative investigations of Earth system processes. By systematically archiving detailed geochemical (meta-)data in structured schemas, intractably large datasets comprising thousands of analyses produced by numerous laboratories can be readily interrogated in novel and powerful ways. These include rapid derivation of inter-data relationships, facilitating on-the-fly data compilation, analysis, and visualisation.
Constraints on the current rate of deformation and surface uplift of the Australian continent from a new seismic database and low T thermochronological data.
Australian Journal of Earth Sciences, Vol. 56, 2, pp. 99-110.
Abstract: The fragmentary Phanerozoic geological record of the anomalously elevated Zimbabwe Craton makes reconstructing its history difficult using conventional field methods. Here we constrain the cryptic Phanerozoic evolution of the Zimbabwe Craton using a spatially extensive apatite (U-Th-Sm)/He (AHe), apatite fission track (AFT), and zircon (U-Th)/He (ZHe) data set. Joint thermal history modeling reveals that the region experienced two cooling episodes inferred to be the denudational response to surface uplift. The first and most significant protracted denudation period was triggered by stress transmission from the adjacent ~750-500 Ma Pan-African orogenesis during the amalgamation of Gondwana. The spatial extent of this rejuvenation signature, encompassing the current broad topographic high, could indicate the possible longevity of an ancient topographic feature. The ZHe data reveal a second, minor denudation phase which began in the Paleogene and removed a kilometer-scale Karoo cover from the craton. Within our data set, the majority of ZHe ages are younger than their corresponding AHe and AFT ages, even at relatively low eU. This unexpectedly recurrent age “inversion” suggests that in certain environments, moderately, as well as extremely, damaged zircons have the potential to act as ultra-low-temperature thermochronometers. Thermal history modeling results reveal that the zircon radiation damage accumulation and annealing model (ZRDAAM) frequently overpredicts the ZHe age. However, the opposite is true for extremely damaged zircons where the ZHe and AHe data are also seemingly incompatible. This suggests that modification of the ZRDAAM may be required for moderate to extreme damage levels.
Geostandards and Geoanalysis Research, doi.org/10.1111/GGR.12419 34p. Pdf
Australia
geochemistry
Abstract: To promote a more efficient and transparent geochemistry data ecosystem, a consortium of Australian university research laboratories called the AuScope Geochemistry Network (AGN) assembled to build a collaborative platform for the express purpose of preserving, disseminating, and collating geochronology and isotopic data. In partnership with geoscience-data-solutions company Lithodat Pty Ltd, the open, cloud-based AusGeochem platform (https://ausgeochem.auscope.org.au) was developed to simultaneously serve as a geosample registry, a geochemical data repository, and a data analysis tool. Informed by method-specific groups of geochemistry experts and established international data reporting practices, community-agreed database schemas were developed for rock and mineral geosample metadata and secondary ion mass spectrometry U-Pb analysis, with additional models for laser ablation inductively-coupled mass spectrometry U-Pb and Lu-Hf, Ar-Ar, fission-track and (U-Th-Sm)/He under development. Collectively, the AusGeochem platform provides the geochemistry community with a new, dynamic resource to help facilitate FAIR (Findable, Accessible, Interoperable, Reusable) data management, streamline data dissemination and advanced quantitative investigations of Earth system processes. By systematically archiving detailed geochemical (meta-)data in structured schemas, intractably large datasets comprising thousands of analyses produced by numerous laboratories can be readily interrogated in novel and powerful ways. These include rapid derivation of inter-data relationships, facilitating on-the-fly data compilation, analysis, and visualisation.
Lorencak, M., Kohn, B.P., Osadetz, K.G., Gleadow, A.J.W.
Combined apatite fission track and U Th/He thermochronology in a slowly cooled terrane: results from a 3440 m deep drill hole in the southern Canadian shield.
Earth and Planetary Science Letters, Vol. 227, 1-2, Oct. 30, pp. 87-104.
Hu, S., Raza, A., Min, K., Kohn, B.P., Reiners, Ketcham, Wang, Gleadow
Late Mesozoic and Cenozoic thermotectonic evolution along a transect from the north Chin a craton through the Qinling orogen into the Yangtze craton, central.
Abstract: The origin of intraplate carbonatitic to alkaline volcanism in Africa is controversial. A tectonic control, i.e., decompression melting associated with far-field stress, is suggested by correlation with lithospheric sutures, repeated magmatic cycles in the same areas over several million years, synchronicity across the plate, and lack of clear age progression patterns. Conversely, a dominant role for mantle convection is supported by the coincidence of Cenozoic volcanism with regions of lithospheric uplift, positive free-air gravity anomalies, and slow seismic velocities. To improve constraints on the genesis of African volcanism, here we report the first radiometric and isotopic results for the Catanda complex, which hosts the only extrusive carbonatites in Angola. Apatite (U-Th-Sm)/He and phlogopite 40Ar/39Ar ages of Catanda aillikite lavas indicate eruption at ca. 500-800 ka, more than 100 m.y. after emplacement of abundant kimberlites and carbonatites in this region. The lavas share similar high-? (HIMU)-like Sr-Nd-Pb-Hf isotope compositions with other young mantle-derived volcanics from Africa (e.g., Northern Kenya Rift; Cameroon Line). The position of the Catanda complex in the Lucapa corridor, a long-lived extensional structure, suggests a possible tectonic control for the volcanism. The complex is also located on the Bié Dome, a broad region of fast Pleistocene uplift attributed to mantle upwelling. Seismic tomography models indicate convection of deep hot material beneath regions of active volcanism in Africa, including a large area encompassing Angola and northern Namibia. This is strong evidence that intraplate late Cenozoic volcanism, including the Catanda complex, resulted from the interplay between mantle convection and preexisting lithospheric heterogeneities.
Mineral inclusions in sublithospheric diamonds from Collier 4 kimberlite pipe, Juina, Brazil: subducted protoliths, carbonated melts and primary kimberlite ..
Contributions to Mineralogy and Petrology, Vol. 160, 4, pp. 489-50.
Abstract: Raman spectroscopy is widely applied in metamorphic petrology and offers many opportunities for geological and tectonic research. Minimal sample preparation preserves sample integrity and microtextural information, while use with confocal microscopes allows spatial resolution down to the micrometer level. Raman spectroscopy clearly distinguishes mineral polymorphs, providing crucial constraints on metamorphic conditions, particularly ultrahigh-pressure conditions. Raman spectroscopy can also be used to monitor the structure of carbonaceous material in metamorphic rocks. Changes in structure are temperature-sensitive, so Raman spectroscopy of carbonaceous material is widely used for thermometry. Raman spectroscopy can also detect and quantify strain in micro-inclusions, offering new barometers that can be applied to understand metamorphic and tectonic processes without any assumptions about chemical equilibrium.
Developments in FTIR spectroscopy of diamond ( part 1): nitrogen aggregation in zoned diamonds, the timing of diamond growth and the thermal history of the lithosphere.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 16438 Abstract
Africa, Zimbabwe, Australia, South America, Brazil
Deposit - Murowa, Argyle, Machado River
Abstract: Fourier Transform Infrared (FTIR) spectroscopy is a commonly-used technique for investigating diamonds. It gives the most useful information if spatially-resolved measurements are used [1]. In this contribution we discuss the best way to acquire and present FTIR data from diamonds, using examples from Murowa (Zimbabwe), Argyle (Australia) and Machado River (Brazil). Examples of FTIR core-to-rim line scans, maps with high spatial resolution and maps with high spectral resolution that are fitted to extract the spatial variation of different nitrogen and hydrogen defects are presented. Model mantle residence temperatures are calculated from the concentration of A and B nitrogen-containing defects in the diamonds using known times of annealing in the mantle. A new, two-stage thermal annealing model is presented that better constrains the thermal history of the diamond and that of the mantle lithosphere in which the diamond resided. The effect of heterogeneity within the analysed FTIR volume is quantitatively assessed and errors in model temperatures that can be introduced by studying whole diamonds instead of thin plates are discussed. The kinetics of platelet growth and degradation will be discussed and the potential for two separate, kinetically-controlled defect reactions to be used to constrain a full thermal history of the diamond will be assessed. [1] Kohn, S.C., Speich, L., Smith, C.B. and Bulanova, G.P., 2016. FTIR thermochronometry of natural diamonds: A closer look.
Abstract: We performed laser-heated diamond anvil cell experiments on bulk compositions in the systems MgO-SiO2-H2O (MSH) and MgO-Al2O3-SiO2-H2O (MASH) that constrain the stability of hydrous phases in Earth’s lower mantle. Phase identification by synchrotron powder diffraction reveals a consistent set of stability relations for the high-pressure, dense hydrous silicate phases D and H. In the MSH system phase D is stable to ~ 50 GPa, independent of temperature from ~ 1300 to 1700 K. Phase H becomes stable between 35 and 40 GPa, and the phase H out reaction occurs at ~ 55 GPa at 1600 K with a negative dT/dP slope of ~ -75 K/GPa. Between ~ 30 and 50 GPa dehydration melting occurs at ~ 1800K with a flat dT/dP slope. A cusp along the solidus at ~ 50 GPa corresponds with the intersection of the subsolidus phase H out reaction, and the dT/dP melting slope steepens to ~ 15 K/GPa up to ~ 85 GPa.
Earth and Planetary Science Letters, Vol. 432, pp. 374-380.
South America, Brazil
Deposit - Juina-5, Collier-4, Machado River
Abstract: Sub-lithospheric diamonds from the Juina-5 and Collier-4 kimberlites and the Machado River alluvial deposit in Brazil have carbon isotopic compositions that co-vary with the oxygen isotopic compositions of their inclusions, which implies that they formed by a mixing process. The proposed model for this mixing process, based on interaction of slab-derived carbonate melt with reduced (carbide- or metal-bearing) ambient mantle, explains these isotopic observations. It is also consistent with the observed trace element chemistries of diamond inclusions from these localities and with the experimental phase relations of carbonated subducted crust. The 18O-enriched nature of the inclusions demonstrates that they incorporate material from crustal protoliths that previously interacted with seawater, thus confirming the subduction-related origin of superdeep diamonds. These samples also provide direct evidence of an isotopically anomalous reservoir in the deep (?350 km) mantle.
Abstract: Interactions between crustal and mantle reservoirs dominate the surface inventory of volatile elements over geological time, moderating atmospheric composition and maintaining a life-supporting planet. While volcanoes expel volatile components into surface reservoirs, subduction of oceanic crust is responsible for replenishment of mantle reservoirs. Many natural, 'superdeep' diamonds originating in the deep upper mantle and transition zone host mineral inclusions, indicating an affinity to subducted oceanic crust. Here we show that the majority of slab geotherms will intersect a deep depression along the melting curve of carbonated oceanic crust at depths of approximately 300 to 700 kilometres, creating a barrier to direct carbonate recycling into the deep mantle. Low-degree partial melts are alkaline carbonatites that are highly reactive with reduced ambient mantle, producing diamond. Many inclusions in superdeep diamonds are best explained by carbonate melt-peridotite reaction. A deep carbon barrier may dominate the recycling of carbon in the mantle and contribute to chemical and isotopic heterogeneity of the mantle reservoir.
Abstract: Diamonds from the Machado River alluvial deposit have been characterised on the basis of external morphology, internal textures, carbon isotopic composition, nitrogen concentration and aggregation state and mineral inclusion chemistry. Variations in morphology and features of abrasion suggest some diamonds have been derived directly from local kimberlites, whereas others have been through extensive sedimentary recycling. On the basis of mineral inclusion compositions, both lithospheric and sublithospheric diamonds are present at the deposit. The lithospheric diamonds have clear layer-by-layer octahedral and/or cuboid internal growth zonation, contain measurable nitrogen and indicate a heterogeneous lithospheric mantle beneath the region. The sublithospheric diamonds show a lack of regular sharp zonation, do not contain detectable nitrogen, are isotopically heavy (?13CPDB predominantly ? 0.7 to ? 5.5) and contain inclusions of ferropericlase, former bridgmanite, majoritic garnet and former CaSiO3-perovskite. This suggests source lithologies that are Mg- and Ca-rich, probably including carbonates and serpentinites, subducted to lower mantle depths. The studied suite of sublithospheric diamonds has many similarities to the alluvial diamonds from Kankan, Guinea, but has more extreme variations in mineral inclusion chemistry. Of all superdeep diamond suites yet discovered, Machado River represents an end-member in terms of either the compositional range of materials being subducted to Transition Zone and lower mantle or the process by which materials are transferred from the subducted slab to the diamond-forming region.
Abstract: The trace element compositions of inclusions in sub-lithospheric diamonds from the Juina-5 kimberlite, Brazil, are presented. Literature data for mineral/melt partition coefficients were collated, refitted and employed to interpret inclusion compositions. As part of this process an updated empirical model for predicting the partitioning behaviour of trivalent cations for garnet-melt equilibrium calibrated using data from 73 garnet-melt pairs is presented. High levels of trace element enrichment in inclusions interpreted as former calcium silicate perovskite and majoritic garnet preclude their origin as fragments of an ambient deep mantle assemblage. Inclusions believed to represent former bridgmanite minerals also display a modest degree of enrichment relative to mantle phases. The trace element compositions of ‘NAL’ and ‘CF phase’ minerals are also reported. Negative Eu, Ce, and Y/Ho anomalies alongside depletions of Sr, Hf and Zr in many inclusions are suggestive of formation from a low-degree carbonatitic melt of subducted oceanic crust. Observed enrichments in garnet and ‘calcium perovskite’ inclusions limit depths of melting to less than ~ 600 km, prior to calcium perovskite saturation in subducting assemblages. Less enriched inclusions in sub-lithospheric diamonds from other global localities may represent deeper diamond formation. Modelled source rock compositions that are capable of producing melts in equilibrium with Juina-5 ‘calcium perovskite’ and majorite inclusions are consistent with subducted MORB. Global majorite inclusion compositions suggest a common process is responsible for the formation of many superdeep diamonds, irrespective of geographic locality. Global transition zone inclusion compositions are reproduced by fractional crystallisation from a single parent melt, suggesting that they record the crystallisation sequence and melt evolution during this interaction of slab melts with ambient mantle. All observations are consistent with the previous hypothesis that many superdeep diamonds are created as slab-derived carbonatites interact with peridotitic mantle in the transition zone.
Africa, Zimbabwe, Australia, South America, Brazil
Deposit - Murowa, Argyle, Machado River
Abstract: Fourier Transform Infrared (FTIR) spectroscopy is a commonly-used technique for investigating diamonds, that gives the most useful information if spatially-resolved measurements are used. In this paper we discuss the best way to acquire and present FTIR data from diamonds, using examples from Murowa (Zimbabwe), Argyle (Australia) and Machado River (Brazil). Examples of FTIR core-to-rim line scans, maps with high spatial resolution and maps with high spectral resolution that are fitted to extract the spatial variation of different nitrogen and hydrogen defects are presented. Model mantle residence temperatures are calculated from the concentration of A and B nitrogen-containing defects in the diamonds using known times of annealing in the mantle. A new, two-stage thermal annealing model is presented that better constrains the thermal history of the diamond and that of the mantle lithosphere in which the diamond resided. The effect of heterogeneity within the analysed FTIR volume is quantitatively assessed and errors in model temperatures that can be introduced by studying whole diamonds instead of thin plates are discussed. The spatial distribution of VN3H hydrogen defects associated with the 3107 cm? 1 vibration does not follow the same pattern as nitrogen defects, and an enrichment of VN3H hydrogen at the boundary between pre-existing diamond and diamond overgrowths is observed. There are several possible explanations for this observation including a change in chemical composition of diamond forming fluid during growth or kinetically controlled uptake of hydrogen.
Abstract: Diamonds from Dachine, French Guiana, are unique among worldwide diamond populations. The diamonds were transported to the surface in an unusual ultramafic extrusive magma with an affinity to boninite or komatiite, which was emplaced within an arc geological setting at ~ 2.2 Ga. Dachine diamonds have internal and external morphologies indicative of relatively rapid growth from carbon oversaturated fluids or melts, and exhibit internal features consistent with residence in a high-strain environment. On the basis of nitrogen (N) defects the diamonds are categorized as Type Ib-IaA. The unusually low aggregation state of N places severe constraints on the thermal history of the diamonds, effectively ruling out derivation in convecting mantle. The carbon and N isotopic compositions of Dachine diamonds are consistent with a sedimentary source of carbon, with the majority of diamonds having ?13C values < ? 25‰ and ?15N values > + 4‰. The primary carbon was presumably deposited on an early Proterozoic seafloor. Sulphide inclusions have low Ni and Cr and are comparable to lithospheric eclogitic-type sulphide inclusions. Three garnet and one clinopyroxene inclusion are also eclogitic in composition, and one garnet inclusion has a majorite component indicating an origin around 250 km depth. The silicate inclusions are highly depleted in many incompatible trace elements (e.g. LREE, Nb, Hf, Zr), and modelling indicates an eclogitic source lithology that contained a LREE-enriched trace phase such as epidote or allanite, and an HFSE-rich phase such as rutile. Four of the five inclusions are unusually enriched in Mn, as well as Ni and Co, and modelling indicates a protolith with the bulk composition of subducted normal MORB plus about 10% ferromanganese crust component. We suggest a model wherein Dachine diamonds precipitated from remobilized sedimentary carbon at the slab-mantle interface from liquids derived ultimately by deserpentinization of slab peridotite at depths of ~ 200 to 250 km. These fluids may also trigger melting in wedge peridotite, resulting in a volatile-rich ultramafic melt that transports the diamonds rapidly to the surface. The process of diamond formation and exhumation from the slab mantle interface likely occurred in a Paleoproterozoic subduction zone and over a very limited timespan, likely less than a million years.
Abstract: Jeffbenite, ideally Mg3Al2Si3O8, previously known as tetragonal-almandine-pyrope-phase (‘TAPP’), has been characterized as a new mineral from an inclusion in an alluvial diamond from São Luiz river, Juina district of Mato Grosso, Brazil. Its density is 3.576 g/cm3 and its microhardness is ?7. Jeffbenite is uniaxial (-) with refractive indexes ??=?1.733(5) and ??=?1.721(5). The crystals are in general transparent emerald green. Its approximate chemical formula is (Mg2.62Fe2+0.27)(Al1.86Cr0.16)(Si2.82Al0.18)O12 with very minor amounts of Mn, Na and Ca. Laser ablation ICP-MS showed that jeffbenite has a very low concentration of trace elements. Jeffbenite is tetragonal with space group I4¯2d, cell edges being a?=?6.5231(1) and c?=?18.1756(3) Å. The main diffraction lines of the powder diagram are [d (in Å), intensity, hkl]: 2.647, 100, 2 0 4; 1.625, 44, 3 2 5; 2.881, 24, 2 1 1; 2.220, 19, 2 0 6; 1.390, 13, 4 2 4; 3.069, 11, 2 0 2; 2.056, 11, 2 2 4; 1.372, 11, 2 0 12. The structural formula of jeffbenite can be written as (M1)(M2)2(M3)2(T1)(T2)2O12 with M1 dominated by Mg, M2 dominated by Al, M3 dominated again by Mg and both T1 and T2 almost fully occupied by Si. The two tetrahedra do not share any oxygen with each other (i.e. jeffbenite is classified as an orthosilicate). Jeffbenite was approved as a new mineral by the IMA Commission on New Minerals and Mineral Names with the code IMA 2014-097. Its name is after Jeffrey W. Harris and Ben Harte, two world-leading scientists in diamond research. The petrological importance of jeffbenite is related to its very deep origin, which may allow its use as a pressure marker for detecting super-deep diamonds. Previous experimental work carried out on a Ti-rich jeffbenite establishes that it can be formed at 13 GPa and 1700 K as maximum P-T conditions.
Abstract: Platelets in diamond are extended planar defects that are thought to be generated during the nitrogen aggregation process in type Ia diamonds. They were subjected to intensive research during the 1980s and 1990s but the techniques used for observation of defects in diamond have improved since that time and new insights can be gained by further study. This study combines high resolution Fourier Transform Infrared (FTIR) analysis, with an emphasis on the main platelet peak, and transmission electron microscopic (TEM) imaging. By performing TEM and FTIR analyses on volumes of diamond that were closely spatially related it is shown that the average platelet diameter, D, follows the relationship D=ax?b where x is the position of the platelet peak in the infrared spectrum, a is a constant and b is the minimum position of the platelet peak. The best fit to the data is obtained if a value of b=1360cm?1 is used, giving a fitted value of a=221. The observed variation in infrared (IR) peak width can also be explained in terms of this relationship. Additionally, platelet morphology was found to vary according to diameter with large platelets being more elongated. The tendency to become more elongated can be described by the empirical equation AR=11.9D+19.6+0.4 where AR is the aspect ratio. Using the relationships established here, it will be possible to study platelet abundance and size as a function of parameters such as nitrogen concentration, nitrogen aggregation and diamond residence time in the mantle. This work therefore will open up new methods for constraining the geological history of diamonds of different parageneses and from different localities.
Africa, Zimbabwe. Australia, Canada, Northwest Territories, South Africa, Botswana
deposit - Murowa, Argyle, Diavik, Venetia, Orapa
Abstract: FTIR maps of diamond plates, cut through the centre of growth, contain abundant information about changing defect concentrations from core to rim. These data can, in principle, be interpreted in terms of the variation in conditions of diamond growth and the temperatures experienced by the diamond during the period of mantle residence between growth and exhumation. Many diamonds show multiple growth zones that can be observed by cathodoluminescence. Importantly, the combination of nitrogen concentration and nitrogen aggregation measured by FTIR can be used to determine whether the growth zones are of similar or very different ages (Kohn et al., 2016). In this study, we use automated fitting of several thousand individual spectra within each FTIR map to define a model temperature for each pixel using the Python program, QUIDDIT. We then use a two-stage aggregation model to constrain potential temperature-time histories for each diamond. To take full advantage of the temperature history recorded by zoned diamonds, radiometric ages of inclusions are required. If the growth ages of each zone and the date of exhumation are well-known, then a model temperature can be calculated for each zone. The combination of zone-specific ages and improved quality and processing of FTIR spectra is able to provide unique new insights into the thermal history of diamondbearing lithospheric mantle. For the first time we will be able to use the N defects in diamonds to work out whether a particular location in the lithosphere has heated or cooled over long periods of geological time. The implications for the mechanism of formation of lithosphere will be discussed. We will illustrate the approach using examples of zoned diamonds from Murowa (Zimbabwe), Argyle (Australia), Diavik (Canada), Venetia (South Africa) and Orapa (Botswana).
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 425-
Contributions to Mineralogy and Petrology, Vol. 173, pp. 39-
Global
FTIR
Abstract: Platelets are one of the most common defects occurring in natural diamonds but their behaviour has not previously been well understood. Recent technical advances, and a much improved understanding of the correct interpretation of the main infrared (IR) feature associated with platelets (Speich et al. 2017), facilitated a systematic study of platelets in 40 natural diamonds. Three different types of platelet behaviour were identified here. Regular diamonds show linear correlations between both B-centre concentrations and platelet density and also between platelet size and platelet density. Irregular diamonds display reduced platelet density due to platelet breakdown, anomalously large or small platelets and a larger platelet size distribution. These features are indicative of high mantle storage temperatures. Finally, a previously unreported category of subregular diamonds is defined. These diamonds experienced low mantle residence temperatures and show smaller than expected platelets. Combining the systematic variation in platelet density with temperatures of mantle storage, determined by nitrogen aggregation, we can demonstrate that platelet degradation proceeds at a predictable rate. Thus, in platelet-bearing diamonds where N aggregation is complete, an estimate of annealing temperature can now be made for the first time.
IN: Deep carbon: past to present, Orcutt, Daniel, Dasgupta eds., pp. 89-128.
Mantle
geodynamics
Abstract: The science of studying diamond inclusions for understanding Earth history has developed significantly over the past decades, with new instrumentation and techniques applied to diamond sample archives revealing the stories contained within diamond inclusions. This chapter reviews what diamonds can tell us about the deep carbon cycle over the course of Earth’s history. It reviews how the geochemistry of diamonds and their inclusions inform us about the deep carbon cycle, the origin of the diamonds in Earth’s mantle, and the evolution of diamonds through time.
IN: Deep Carbon: past to present. Editors Orcutt, Danielle, Dasgupta, pp. 89-128.
Mantle
geodynamics
Abstract: The science of studying diamond inclusions for understanding Earth history has developed significantly over the past decades, with new instrumentation and techniques applied to diamond sample archives revealing the stories contained within diamond inclusions. This chapter reviews what diamonds can tell us about the deep carbon cycle over the course of Earth’s history. It reviews how the geochemistry of diamonds and their inclusions inform us about the deep carbon cycle, the origin of the diamonds in Earth’s mantle, and the evolution of diamonds through time.
Computers & Geosciences, doi: 10.1016/j.cageo. 2020.104558 available 30p. Pdf
Global
QUIDDIT
Abstract: Goal: QUIDDIT (QUantification of Infrared-active Defects in Diamond and Inferred Temperatures) is a novel Python application for fast and automated processing of IR spectra of diamond. It was first developed for the work presented in previous studies (Kohn et al., 2016; Speich et al. 2017 and 2018) and has been used in our lab successfully. The goal of this project is to enhance the software and provide easy access to users in research and industry alike. Read the "Project Log" section for more information.
Abstract: QUIDDIT is a free Python software-package designed to process Fourier Transform Infrared (FTIR) spectra of diamonds automatically and efficiently. Core capabilities include baseline correction, determination of nitrogen concentration, nitrogen aggregation state and model temperature and fitting of both the 3107 cm-1 and platelet (B’) peaks. These capabilities have allowed the authors to study platelet defects and their relationship to nitrogen aggregation in previous studies. Data visualisation, vital to interpreting and evaluating results, is another key component of the software. QUIDDIT can be applied to single spectra as well as linescan and 2-dimensional map data. Recently, additional features such as manual platelet peak and nitrogen fitting, custom batch peak fitting and two-stage aggregation modelling were made available. QUIDDIT has been used successfully for natural diamonds containing aggregated forms of nitrogen in the past and has since been adapted for the study of diamonds containing C-centres as well.
Journal of Geophysical Research, Solid Earth, in press available, 34p.
Global
diamond inclusions
Abstract: Natural diamonds, as well as being a cherished commodity, are valuable for scientists studying the Earth's interior because they only grow at depths greater than 140 km. When diamonds grow, they may trap tiny fragments of surrounding materials as sub?millimetre defects. Study of these inclusions can provide insights into the materials and processes occurring deep inside our planet. Sub?lithospheric diamonds are a relatively rare subset of natural diamonds, believed to have grown deeper than 250 km, and are thought to be the deepest Earth materials that have been transported to the surface. Ideally, we would be able to estimate their formation depths accurately. Inclusions of majoritic garnet provide a unique opportunity for this, as their chemistry is known to change systematically with formation depth. However, this behaviour is highly complex, and previous attempts to parameterise the depth dependence of inclusion chemistries have limitations. Here we have used data science to train a "Machine Learning" algorithm that improves the accuracy of estimating the formation pressures of majoritic garnet inclusion. The approach confirms that many natural diamonds containing inclusions of majoritic garnet must have originally formed at depths of 400 - 660 km.
Journal of Geophysical Research Physical Review B., http://doi.org/10 /1029/2020JB020 604 21p. Pdf
Mantle
diamond inclusions
Abstract: Natural diamonds, as well as being a cherished commodity, are valuable for scientists studying the Earth's interior because they only grow at depths greater than 140 km. When diamonds grow, they may trap tiny fragments of surrounding materials as sub?millimeter defects. Study of these inclusions can provide insights into the materials and processes occurring deep inside our planet. Sub?lithospheric diamonds are a relatively rare subset of natural diamonds, believed to have grown deeper than 250 km, and are thought to be the deepest Earth materials that have been transported to the surface. Ideally, we would be able to estimate their formation depths accurately. Inclusions of majoritic garnet provide a unique opportunity for this, as their chemistry is known to change systematically with formation depth. However, this behavior is highly complex, and previous attempts to parameterize the depth dependence of inclusion chemistries have limitations. Here we have used data science to train a "machine learning" algorithm that improves the accuracy of estimating the formation pressures of majoritic garnet inclusion. The approach confirms that many natural diamonds containing inclusions of majoritic garnet must have originally formed at depths of 400-660 km.
Journal of Metamorphic Geology, Vol. 35, 6, pp. 631-661.
Mantle
geothermometry
Abstract: The Proterozoic belts that occur along the margins of the West Australian Craton, as well as those in intraplate settings, generally share similar geological histories that suggest a common plate-margin driver for orogeny. However, the thermal drivers for intraplate orogenesis are more poorly understood. The Mutherbukin Tectonic Event records a protracted period of Mesoproterozoic reworking of the Capricorn Orogen and offers significant insight into both the tectonic drivers and heat sources of long-lived intraplate orogens. Mineral assemblages and tectonic fabrics related to this event occur within a 50 km-wide fault-bound corridor in the central part of the Gascoyne Province in Western Australia. This zone preserves a crustal profile, with greenschist facies rocks in the north grading to upper amphibolite facies rocks in the south. The P–T–t evolution of 13 samples from 10 localities across the Mutherbukin Zone is investigated using phase equilibria modelling integrated with in situ U–Pb monazite and zircon geochronology. Garnet chemistry from selected samples is used to further refine the P–T history and shows that the dominant events recorded in this zone are prolonged D1 transpression between c. 1,320 and 1,270 Ma, followed by D2 transtension from c. 1,210 to 1,170 Ma. Peak metamorphic conditions in the mid-crust reached >650°C and 4.4–7 kbar at c. 1,210–1,200 Ma. Most samples record a single clockwise P–T evolution during this event, although some samples might have experienced multiple perturbations. The heat source for metamorphism was primarily conductive heating of radiogenic mid- and upper crust, derived from earlier crustal differentiation events. This crust was thickened during D1 transpression, although the thermal effects persisted longer than the deformation event. Peak metamorphism was terminated by D2 transtension at c. 1,210 Ma, with subsequent cooling driven by thinning of the radiogenic crust. The coincidence of a sedimentary basin acting as a thermal lid and a highly radiogenic mid-crustal batholith restricted to the Mutherbukin Zone accounts for reworking being confined to a discrete crustal corridor. Our results show that radiogenic regions in the shallow to mid crust can elevate the thermal gradient and localize deformation, causing the crust to be more responsive to far-field stresses. The Mutherbukin Tectonic Event in the Capricorn Orogen was synchronous with numerous Mesoproterozoic events around the West Australian Craton, suggesting that thick cratonic roots play an important role in propagating stresses generated at distant plate boundaries.
Gem News. the Golconda "d" Diamond Resurfaces. John Sinkankas Provides Information on Diamonds in Thailand. a Diamond Is Melted in Laboratory. Punch Jones Diamond.
Gems And Gemology, Vol. 32, WINTER PP. 242-243.
India, Thailand, Russia, United States, Great Lakes
Gems news:India -Tanna and Chatapur areas. Japan -largestsyntheticdiamond. South Africa - Diamond inclusions in pyrope.Sri Lanka - geological exploration d
Gems and Gemology, Vol. 22, No. 1, Spring pp. 54-55
High pressure phase transitions and subduction behaviour of continent crust at pressure temperature conditions up to the upper part of the lower mantle.
Earth and Planetary Science Letters, Vol. 357-358, pp. 31-41.
Akaogi, M., Kawahara, A., Kojitani, H., Yoshida, K., Anegawa, Y., Ishii, T.
High pressure phase transitions in MgCr2O4 MgSiO4 composition: reactions between olivine and chromite with implications for ultrahigh pressure chromitites.
Aravanis, T., Chen, J., Fuechsle, M., Grujic, M., Johnston, P., Kok, Y., Magaraggia, R., Mann, A., Mann, L., McIntoshm S., Rheinberger, G., Saxey, D., Smalley, M., van Kann, F., Walker, G., Winterflood, J.
Abstract: The minerals exploration industry’s demand for a highly precise airborne gravity gradiometer has driven development of the VK1TM Airborne Gravity Gradiometer, a collaborative effort by Rio Tinto and the University of Western Australia. VK1TM aims to provide gravity gradient data with lower uncertainty and higher spatial resolution than current commercial systems. In the recent years of VK1TM development, there have been significant improvements in hardware, signal processing and data processing which have combined to result in a complete AGG system that is approaching competitive survey-ready status. This paper focuses on recent improvements. Milestone-achieving data from recent lab-based and moving-platform trials will be presented and discussed, along with details of some advanced data processing techniques that are required to make the most use of the data.
Journal of the Geological Society of India, Vol. 91, pp. 135-146.
India
Alkaline - Prakasam
Abstract: Three distinct alkaline magmas, represented by shonkinite, lamprophyre and alkali basalt dykes, characterize a significant magmatic expression of rift-related mantle-derived igneous activity in the Mesoproterozoic Prakasam Alkaline Province, SE India. In the present study we have estimated emplacement velocities (ascent rates) for these three varied alkaline magmas and compared with other silicate magmas to explore composition control on the ascent rates. The alkaline dykes have variable widths and lengths with none of the dykes wider than 1 m. The shonkinites are fine- to medium-grained rocks with clinopyroxene, phologopite, amphibole, K-feldspar perthite and nepheline as essential minerals. They exhibit equigranular hypidiomorphic to foliated textures. Lamprophyres and alkali basalts characteristically show porphyritic textures. Olivine, clinopyroxene, amphibole and biotite are distinct phenocrysts in lamprophyres whereas olivine, clinopyroxene and plagioclase form the phenocrystic mineralogy in the alkali basalts. The calculated densities [2.54-2.71 g/cc for shonkinite; 2.61-2.78 g/cc for lamprophyre; 2.66-2.74 g/cc for alkali basalt] and viscosities [3.11-3.39 Pa s for shonkinite; 3.01-3.28 Pa s for lamprophyre; 2.72-3.09 Pa s for alkali basalt] are utilized to compute velocities (ascent rates) of the three alkaline magmas. Since the lamprophyres and alkali basalts are crystal-laden, we have also calculated effective viscosities to infer crystal control on the velocities. Twenty percent of crystals in the magma increase the viscosity by 2.7 times consequently decrease ascent rate by 2.7 times compared to the crystal-free magmas. The computed ascent rates range from 0.11-2.13 m/sec, 0.23-2.77 m/sec and 1.16-2.89 m/sec for shonkinite, lamprophyre and alkali basalt magmas respectively. Ascent rates increase with the width of the dykes and density difference, and decrease with magma viscosity and proportion of crystals. If a constant width of 1 m is assumed in the magma-filled dyke propagation model, then the sequence of emplacement velocities in the decreasing order is alkaline magmas (4.68-15.31 m/sec) > ultramafic-mafic magmas (3.81-4.30 m/sec) > intermediate-felsic magmas (1.76-2.56 m/sec). We propose that SiO2 content in the terrestrial magmas can be modeled as a semi-quantitative "geospeedometer" of the magma ascent rates.
Journal of the Geological Society of India, Vol. 91, 3, pp. 263-272.
India
shonkinite
Abstract: Formation of the fragments of the wall-rock during dyking is one of the important manifestations of instantaneous magmatic events. This process is well documented at shallower depths of Earth’s crust but not at deeper levels. In this paper the in situ xenoliths of host rock nepheline syenite within a micro-shonkinite dyke emplaced at mid-crustal depths is described and the fractal theory applied to evaluate origin of the xenoliths. The nepheline syenite xenoliths are angular to oval shaped and sub-millimetre to ~50 cm long. The xenoliths are matrix supported with clasts and matrix being in equal proportions. Partly detached wall-rock fragments indicate incipient xenolith formation, which suggested that the model fragmentation processes is solely due to dyke emplacement. Fractal analytical techniques including clast size distribution, boundary roughness fractal dimension and clast circularity was carried out. The fractal data suggests that hydraulic (tensile) fracturing is the main process of host rock brecciation. However, the clast size and shape are further affected by postfragmentation processes including shear and thermal fracturing, and chemical erosion. The study demonstrates that dyking in an isotropic medium produces fractal size distributions of host rock xenoliths; however, post-fragmentation processes modify original fractal size distributions.
Journal of the Geological Society of India, Vol. 91, 2, pp. 135-146.
India
Prakasam alkaline province
Abstract: Three distinct alkaline magmas, represented by shonkinite, lamprophyre and alkali basalt dykes, characterize a significant magmatic expression of rift-related mantle-derived igneous activity in the Mesoproterozoic Prakasam Alkaline Province, SE India. In the present study we have estimated emplacement velocities (ascent rates) for these three varied alkaline magmas and compared with other silicate magmas to explore composition control on the ascent rates. The alkaline dykes have variable widths and lengths with none of the dykes wider than 1 m. The shonkinites are fine- to medium-grained rocks with clinopyroxene, phologopite, amphibole, K-feldspar perthite and nepheline as essential minerals. They exhibit equigranular hypidiomorphic to foliated textures. Lamprophyres and alkali basalts characteristically show porphyritic textures. Olivine, clinopyroxene, amphibole and biotite are distinct phenocrysts in lamprophyres whereas olivine, clinopyroxene and plagioclase form the phenocrystic mineralogy in the alkali basalts. The calculated densities [2.54-2.71 g/cc for shonkinite; 2.61-2.78 g/cc for lamprophyre; 2.66-2.74 g/cc for alkali basalt] and viscosities [3.11-3.39 Pa s for shonkinite; 3.01-3.28 Pa s for lamprophyre; 2.72-3.09 Pa s for alkali basalt] are utilized to compute velocities (ascent rates) of the three alkaline magmas. Since the lamprophyres and alkali basalts are crystal-laden, we have also calculated effective viscosities to infer crystal control on the velocities. Twenty percent of crystals in the magma increase the viscosity by 2.7 times consequently decrease ascent rate by 2.7 times compared to the crystal-free magmas. The computed ascent rates range from 0.11-2.13 m/sec, 0.23-2.77 m/sec and 1.16-2.89 m/sec for shonkinite, lamprophyre and alkali basalt magmas respectively. Ascent rates increase with the width of the dykes and density difference, and decrease with magma viscosity and proportion of crystals. If a constant width of 1 m is assumed in the magma-filled dyke propagation model, then the sequence of emplacement velocities in the decreasing order is alkaline magmas (4.68-15.31 m/sec) > ultramafic-mafic magmas (3.81-4.30 m/sec) > intermediate-felsic magmas (1.76-2.56 m/sec). We propose that SiO2 content in the terrestrial magmas can be modeled as a semi-quantitative “geospeedometer” of the magma ascent rates.
Geophysical Research Letters, orchid.org/ 0000-0001-9945-6945
Canada, Northwest Territories
permafrost
Abstract: The origin of the complex pattern of SKS splitting over the western United States (U.S.) remains a long-lasting debate, where a model that simultaneously matches the various SKS features is still lacking. Here we present a series of quantitative geodynamic models with data assimilation that systematically evaluate the influence of different lithospheric and mantle structures on mantle flow and seismic anisotropy. These tests reveal a configuration of mantle deformation more complex than ever envisioned before. In particular, we find that both lithospheric thickness variations and toroidal flows around the Juan de Fuca slab modulate flow locally, but their co-existence enhances large-scale mantle deformation below the western U.S. The ancient Farallon slab below the east coast pulls the western U.S. upper mantle eastward, spanning the regionally extensive circular pattern of SKS splitting. The prominent E-W oriented anisotropy pattern within the Pacific Northwest reflects the existence of sustaining eastward intrusion of the hot Pacific oceanic mantle to beneath the continental interior, from within slab tears below Oregon to under the Snake River Plain and the Yellowstone caldera. This work provides an independent support to the formation of intra-plate volcanism due to intruding shallow hot mantle instead of a rising mantle plume.
Tectonic history of the Illinois Basin- an overview
United States Geological Survey (USGS) Open file, United States Geological Survey (USGS)-Missouri G.S. Symp: Mineral resource potential of, p. 19-20. (abstract.)
Abstract: The North Atlantic Craton (NAC) extends along the coasts of southern Greenland. At its northern and southern margins, Archaean rocks are overprinted by Palaeoproterozoic orogeny or overlain by younger rocks. Typical granite-greenstone and granite-gneiss complexes represent the entire Archaean, with a hiatus from ~3.55-3.20 Ga. In the granulite- and amphibolite-facies terranes, the metallogeny comprises hypozonal orogenic gold and Ni-PGE-Cr-Ti-V in mafic-ultramafic magmatic systems. Gold occurrences are widespread around and south of the capital, Nuuk. Nickel mineralization in the Maniitsoq Ni project is hosted in the Norite belt; Cr and PGE in Qeqertarssuatsiaq, and Ti-V in Sinarsuk in the Fiskenæsset complex. The lower-grade metamorphic Isua greenstone belt hosts the >1000 Mt Isua iron deposit in an Eoarchaean banded iron formation. Major Neoarchaean shear zones host mesozonal orogenic gold mineralization over considerable strike length in South-West Greenland. The current metallogenic model of the NAC is based on low-resolution data and variable geological understanding, and prospecting has been the main exploration method. In order to generate a robust understanding of the metal endowment, it is necessary to apply an integrated and collective approach. The NAC is similar to other well-endowed Archaean terranes but is underexplored, and is therefore likely to host numerous targets for greenfields exploration.
Earth Science Reviews , Vol. 215, 103509, 27p. Pdf
Mantle
magmatism
Abstract: Carbonatites are formed from volatile-rich melts, commonly associated with a characteristic hydrothermal footprint. However, studies of their fluid inclusions are relatively scarce and heterogeneous in terms of detail and completeness of the data presented. Here, we review and discuss comprehensively the results of previous studies and derive a general model for the formation and properties of fluids associated with carbonatitic magmatism. Worldwide, four types of fluid inclusion occur in carbonatites: (type I/HS) vapour-poor H2O-NaCl fluids with up to 50 wt% salinity; (type II/HC) vapour-rich H2O-NaCl-CO2 fluids with <5 wt% salinity; (type III/DS) multi-component fluids with high salinity and without CO2; and (type IV/CDS) multi-component fluids with high salinity and high CO2. This global dataset suggests continuous fluid release from deep to shallow-level intrusions. Modelling of the liquidus surface indicates that carbonatite magmas generally exsolve a saline brine (type I/HS). This brine separates/evolves into a Na-K-sulfate-carbonate/bicarbonate-chloride brine with or without CO2 (types III/DS and IV/CDS), trapped together with low salinity CO2-rich fluids produced by immiscibility. Fluid immiscibility is related to rapid pressure release during fast, forceful and discontinuous magma ascent, which we envisage as a "pneumatic jackhammer" model for carbonatite ascent and emplacement. In this model, cyclic and progressive fluid flux via pressure build-up and subsequent catastrophic pressure release results in a self-sustaining crustal ascent of the buoyant, low-viscosity magma. This process allows for rapid and efficient magma ascent, in particular above the brittle-ductile transition zone, where pressures that prevailed during apatite crystallization have been estimated in numerous complexes. Moreover, this model provides an explanation for the apparent absence of shallow carbonatite magma chambers (in a classical sense) and identifies fenitization as a phenomenon induced by both fluids released during magma ascent and residual fluids.
Kolesnichenko, M., Zedgenizov, D., Ragozin, A., Litasov, K.
Water content in olivines of mantle xenoliths from Udachnaya kimberlite pipe, Yakutia.
V.S. Sobolev Institute of Geology and Mineralogy Siberian Branch Russian Academy of Sciences International Symposium Advances in high pressure research: breaking scales and horizons ( Courtesy of N. Poikilenko), Held Sept. 22-26, 2p. Abstract
Abstract: The paper presents new petrographic, major element and Fourier transform infrared (FTIR) spectroscopy data and PT-estimates of whole-rock samples and minerals of a collection of 19 relatively fresh peridotite xenoliths from the Udachnaya kimberlite pipe, which were recovered from its deeper levels. The xenoliths are non-deformed (granular), medium-deformed and highly deformed (porphyroclastic, mosaic-porphyroclastic, mylonitic) lherzolites, harzburgite and dunite. The lherzolites yielded equilibration temperatures (T) and pressures (P) ranging from 913 to 1324 °C and from 4.6 to 6.3 GPa, respectively. The non-deformed and medium-deformed peridotites match the 35 mW/m2 conductive continental geotherm, whereas the highly deformed varieties match the 45 mW/m2 geotherm. The content of water spans 2 ± 1-95 ± 52 ppm in olivine, 1 ± 0.5-61 ± 9 ppm in orthopyroxene, and 7 ± 2-71 ± 30 ppm in clinopyroxene. The amount of water in garnets is negligible. Based on the modal proportions of mineral phases in the xenoliths, the water contents in peridotites were estimated to vary over a wide range from < 1 to 64 ppm. The amount of water in the mantle xenoliths is well correlated with the deformation degree: highly deformed peridotites show highest water contents (64 ppm) and those medium-deformed and non-deformed contain ca. 1 ppm of H2O. The high water contents in the deformed peridotites could be linked to metasomatism of relatively dry diamondiferous cratonic roots by hydrous and carbonatitic agents (fluids/melts), which may cause hydration and carbonation of peridotite and oxidation and dissolution of diamonds. The heterogeneous distribution of water in the cratonic mantle beneath the Udachnaya pipe is consistent with the models of mantle plume or veined mantle structures proposed based on a trace element study of similar xenolithic suits. Mantle metasomatism beneath the Siberian Craton and its triggered kimberlite magmatism could be induced by mantle enrichment in volatiles (H2O, CO2) supplied by numerous subduction zones which surrounded the Siberian continent in Neoproterozoic-Cambrian time.
Abstract: The paper presents new petrographic, major element and Fourier transform infrared (FTIR) spectroscopy data and PT-estimates of whole-rock samples and minerals of a collection of 19 relatively fresh peridotite xenoliths from the Udachnaya kimberlite pipe, which were recovered from its deeper levels. The xenoliths are non-deformed (granular), medium-deformed and highly deformed (porphyroclastic, mosaic-porphyroclastic, mylonitic) lherzolites, harzburgite and dunite. The lherzolites yielded equilibration temperatures (T) and pressures (P) ranging from 913 to 1324 °C and from 4.6 to 6.3 GPa, respectively. The non-deformed and medium-deformed peridotites match the 35 mW/m2 conductive continental geotherm, whereas the highly deformed varieties match the 45 mW/m2 geotherm. The content of water spans 2 ± 1-95 ± 52 ppm in olivine, 1 ± 0.5-61 ± 9 ppm in orthopyroxene, and 7 ± 2-71 ± 30 ppm in clinopyroxene. The amount of water in garnets is negligible. Based on the modal proportions of mineral phases in the xenoliths, the water contents in peridotites were estimated to vary over a wide range from < 1 to 64 ppm. The amount of water in the mantle xenoliths is well correlated with the deformation degree: highly deformed peridotites show highest water contents (64 ppm) and those medium-deformed and non-deformed contain ca. 1 ppm of H2O. The high water contents in the deformed peridotites could be linked to metasomatism of relatively dry diamondiferous cratonic roots by hydrous and carbonatitic agents (fluids/melts), which may cause hydration and carbonation of peridotite and oxidation and dissolution of diamonds. The heterogeneous distribution of water in the cratonic mantle beneath the Udachnaya pipe is consistent with the models of mantle plume or veined mantle structures proposed based on a trace element study of similar xenolithic suits. Mantle metasomatism beneath the Siberian Craton and its triggered kimberlite magmatism could be induced by mantle enrichment in volatiles (H2O, CO2) supplied by numerous subduction zones which surrounded the Siberian continent in Neoproterozoic-Cambrian time.
Russian Geology and Geophysics, Vol. 59, 7, pp. 763-779.
Russia, Siberia
deposit - Udachnaya
Abstract: A comprehensive study of 26 mafic mantle xenoliths from the Udachnaya kimberlite pipe was carried out. The contents of major and trace elements, equilibrium temperature parameters, and water content in the rock-forming minerals were determined. The temperatures of formation of the studied rocks are estimated at 800-1300 °C. According to IR spectroscopy data, the water content in clinopyroxenes from the studied eclogites varies from values below the detection limit to 99 ppm. The IR spectra of garnets lack bands of water. The water content in clinopyroxene and orthopyroxene from garnet websterite is 72 and 8 ppm, respectively. The water content in the average rock, calculated from the ratio of the rock-forming minerals, varies from a few to 55 ppm. No relationship among the water content, equilibrium temperatures, and rock composition is established. The low water contents in the eclogites are close to the earlier determined water contents in peridotites from the same pipe and are, most likely, due to the re-equilibration of the eclogites with the rocks of the peridotitic lithospheric mantle. The dehydration of the protolith during its subduction and the partial melting of eclogites before their removal by kimberlitic magma to the surface might be an additional cause of the low water contents in the mantle eclogite xenoliths.
Abstract: The water content in the garnet and clinopyroxene in the mantle eclogites from the V. Grib kimberlite pipe (Arkhangelsk Diamondiferous Province, NW Russia) was analysed using Fourier transform infrared spectrometry. The results show that all clinopyroxene grains contained structural water at concentrations of 39 to 247?ppm, whereas two garnet samples contained detectable water at concentrations of 211 and 337?ppm. The low-MgO eclogites with oceanic gabbro precursors contained significantly higher water concentrations in the omphacites (70-247?ppm) and whole rock (35-224?ppm) compared to those with oceanic basalt protoliths (49-73?ppm and 20-36?ppm, respectively). The incorporation of water into the clinopyroxene may be associated with vacancies at the M2 site, Al in the tetrahedral position, and the elements that filled the M2 site (mostly Na and Ca). The highest water content in the omphacite was detected in a nonmetasomatised sample and was assumed to represent residual water that survived during subduction. Other eclogite samples showed signs of modal and/or cryptic metasomatism and contained less water in the omphacites compared to the nonmetasomatised sample. The water content was heterogeneous within the eclogite section of the sampled lithospheric mantle. The lack of distinct and uniform correlations between the indices of eclogite modification and their water content indicated that the saturation with water was disturbed during their residence within the lithospheric mantle.
Aluminum solubility in orthopyroxene in equilibrium with garnet; are interpretation of existing experimental dat a &petrogenetic implications garnet peridotite xenolith
Proceedings of Fifth International Kimberlite Conference held Araxa June, pp. 514-515
Kurszlaukis, S., Mahotkin, I., Rotman, A.Y., Kolesnikov, G.W., Makovchuk, I.V.
Syn and post eruptive volcanic processes in the Yubileinaya kimberlite pipe, Yakutia, Russia and implications for the emplacement of South African style kimberlite
Europe, Fennoscandia, Kola Peninsula, Karelia, Canada
craton
Abstract: Rapid glacio-isostatic rebound in Fennoscandia and Canada that is nonuniform in time and space indicates that there is a layer with strongly decreased viscosity at shallow crustal depths. The upper boundary of the layer is near the depth of 15 km, which corresponds to the maximum depth of earthquake hypocenters in the Precambrian cratons of the Kola Peninsula and Karelia. The position of the lower boundary is less distinct; however, most likely it is located near the base of the crust. The formation of such a layer in the Pliocene-Quaternary occurred due to infiltration of a large volume of mantle fluids into the crust. In many regions, this has led to retrograde metamorphism with rock expansion and a strong decrease in rocks viscosity.
Gertner, I., Tishin, P., Vrublevskii, V., Sazonov, A., Zvyagina, E., Kolmakov, Y.
Neoproterozoic alkaline igneous rocks, carbonatites and gold deposits of the Yenisei Ridge, central Siberia: evidence of mantle plume activity and late collision...
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 169-190.
Abstract: Precambrian supercontinents Nuna-Columbia (1.7 to 1.3 billion years ago) and Rodinia (1.1 to 0.7 billion years ago) have been proposed. However, the arrangements of crustal blocks within these supercontinents are poorly known. Huge, dominantly basaltic magmatic outpourings and intrusions, covering up to millions of square kilometres, termed Large Igneous Provinces, typically accompany (super) continent breakup, or attempted breakup and offer an important tool for reconstructing supercontinents. Here we focus on the Large Igneous Province record for Siberia and Laurentia, whose relative position in Nuna-Columbia and Rodinia reconstructions is highly controversial. We present precise geochronology—nine U -Pb and six Ar -Ar ages—on dolerite dykes and sills, along with existing dates from the literature, that constrain the timing of emplacement of Large Igneous Province magmatism in southern Siberia and northern Laurentia between 1,900 and 720 million years ago. We identify four robust age matches between the continents 1,870, 1,750, 1,350 and 720 million years ago, as well as several additional approximate age correlations that indicate southern Siberia and northern Laurentia were probably near neighbours for this 1.2-billion-year interval. Our reconstructions provide a framework for evaluating the shared geological, tectonic and metallogenic histories of these continental blocks.
Internally consistent thermodynamic dat a set for dense hydrous magnesium silicates up to 35 GPa, 1600 degree C: implications for water circulation in deep mantle.
Physics of the Earth and Planetary Interiors, Vol. 156, 1-2, pp. 89-107.
Abstract: The relative abundance of light elements in the Earth’s core has long been controversial. Recently, the presence of carbon in the core has been emphasized, because the density and sound velocities of the inner core may be consistent with solid Fe7C3. Here we report the longitudinal wave velocity of liquid Fe84C16 up to 70?GPa based on inelastic X-ray scattering measurements. We find the velocity to be substantially slower than that of solid iron and Fe3C and to be faster than that of liquid iron. The thermodynamic equation of state for liquid Fe84C16 is also obtained from the velocity data combined with previous density measurements at 1 bar. The longitudinal velocity of the outer core, about 4% faster than that of liquid iron, is consistent with the presence of 4-5 at.% carbon. However, that amount of carbon is too small to account for the outer core density deficit, suggesting that carbon cannot be a predominant light element in the core.
Diamond & Related Materials, Vol. 109, 108045, 9p. Pdf
Russia
deposit - Aikhal
Abstract: The diversity of the defects in the collection (50 samples) of diamonds from the Aikhal pipe (Yakutia) has been studied with IR, PL, and EPR spectroscopy. The specific features of crystals have been established; the obtained information leads to the discussion about the diamond formation and growth conditions. One of the specific features observed is a high concentration of platelets. According to the platelet behavior, most of the crystals are regular suggesting the growth temperature to be 1100-1200 °C. The concentrations of A and B defects have been evaluated and the same temperature conditions have been obtained according to the Taylor diagram. Using the EPR spectroscopy, the C and N3V centers have been found in many crystals suggesting the aggregation of nitrogen during residence in the mantle at high temperatures. An interesting feature has been observed in the PL spectra. For most crystals, the spectrum with ZPL at 563.5 nm is very intensive. The structure of the observed defect is remaining unknown, the spectrum disappears as a result of annealing at 600 °C indicating the interstitial-vacancy annihilation mechanism.
Diamond and Related Materials, Vol. 109, 108045, 9p. Pdf
Russia
deposit - Aikhal
Abstract: The diversity of the defects in the collection (50 samples) of diamonds from the Aikhal pipe (Yakutia) has been studied with IR, PL, and EPR spectroscopy. The specific features of crystals have been established; the obtained information leads to the discussion about the diamond formation and growth conditions. One of the specific features observed is a high concentration of platelets. According to the platelet behavior, most of the crystals are regular suggesting the growth temperature to be 1100-1200 °C. The concentrations of A and B defects have been evaluated and the same temperature conditions have been obtained according to the Taylor diagram. Using the EPR spectroscopy, the C and N3V centers have been found in many crystals suggesting the aggregation of nitrogen during residence in the mantle at high temperatures. An interesting feature has been observed in the PL spectra. For most crystals, the spectrum with ZPL at 563.5 nm is very intensive. The structure of the observed defect is remaining unknown, the spectrum disappears as a result of annealing at 600 °C indicating the interstitial-vacancy annihilation mechanism.
Physics and Chemistry of Minerals, Vol. 42, 9, pp. 707-722.
South America, Brazil
Deposit - Sao-Luis
Abstract: Photoluminescence (PL) spectroscopy and electron paramagnetic resonance (EPR) were used for the first time to characterize properties of superdeep diamonds from the São-Luis alluvial deposits (Brazil). The infrared measurements showed the low nitrogen content (>50 of 87 diamonds from this locality were nitrogen free and belonged to type IIa) and simultaneously the extremely high level of nitrogen aggregation (pure type IaB being predominant), which indicates that diamonds under study might have formed under high pressure and temperature conditions. In most cases, PL features excited at various wavelengths (313, 473, and 532 nm) were indicative of different growth and post-growth processes during which PL centers could be formed via interaction between vacancies and nitrogen atoms. The overall presence of the 490.7 nm, H3, and H4 centers in the luminescence spectra attests to strong plastic deformations in these diamonds. The neutral vacancy known as the GR1 center has probably occurred in a number of crystals due to radiation damage in the post-growth period. The 558.5 nm PL center is found to be one of the most common defects in type IIa samples which is accompanied by the EPR center with g-factor of 2.00285. The 536 and 576 nm vibronic systems totally dominated the PL spectra of superdeep diamonds, while none of “normal” diamonds from the Mir pipe (Yakutia) with similar nitrogen characteristics showed the latter three PL centers.
Abstract: The behavior of characteristic centers in diamond crystals from the Mir pipe (Yakutia) was investigated upon electron irradiation. A series of diamond crystals of different types was chosen for experiments based on the nitrogen content and aggregation parameters. In electron-irradiated diamonds of the IaAB type, a new characteristic photoluminescence system was found with a zero-phonon line (ZPL) at 615 nm together with phonon replicas of 41 and 90 meV. The phonons' energies pointed to multiphonon interactions with a quasilocal vibration of a vacancy. According to our data, the nitrogen-related defect responsible for this phenomenon contains a vacancy and may be accompanied by some other impurity. Conversely, in an almost nitrogen-free crystal, a specific system with the ZPL at 558 nm was noted. The center in question is known to be vacancy-related and was formed in type IIa crystals from the Mir pipe not only by electron irradiation but also by high-pressure high-temperature annealing when vacancies were released as a result of motion or annihilation of dislocations. Regardless of the nitrogen impurity, specific systems with the ZPL at 454, 491, and 492 nm were registered in the irradiated diamond crystals from the Mir pipe. To examine the generated defects, the irradiated diamond crystals were subjected to low-temperature annealing at ?600 °C. Although the 454 and 491 nm systems persisted, the annealing of the 492 nm system along with well-known 523.6, 489.0, and 503.4 nm (3H) centers indicated the interstitial-vacancy nature of the defect.
Physics and Chemistry of Minerals, In press available 16p.
South America, Brazil, Mato Grosso
Deposit - Juina area
Abstract: Photoluminescence (PL) spectroscopy and electron paramagnetic resonance (EPR) were used for the first time to characterize properties of superdeep diamonds from the São-Luis alluvial deposits (Brazil). The infrared measurements showed the low nitrogen content (>50 of 87 diamonds from this locality were nitrogen free and belonged to type IIa) and simultaneously the extremely high level of nitrogen aggregation (pure type IaB being predominant), which indicates that diamonds under study might have formed under high pressure and temperature conditions. In most cases, PL features excited at various wavelengths (313, 473, and 532 nm) were indicative of different growth and post-growth processes during which PL centers could be formed via interaction between vacancies and nitrogen atoms. The overall presence of the 490.7 nm, H3, and H4 centers in the luminescence spectra attests to strong plastic deformations in these diamonds. The neutral vacancy known as the GR1 center has probably occurred in a number of crystals due to radiation damage in the post-growth period. The 558.5 nm PL center is found to be one of the most common defects in type IIa samples which is accompanied by the EPR center with g-factor of 2.00285. The 536 and 576 nm vibronic systems totally dominated the PL spectra of superdeep diamonds, while none of "normal" diamonds from the Mir pipe (Yakutia) with similar nitrogen characteristics showed the latter three PL centers.
Physics and chemistry of Minerals, Vol. 42, 9, pp. 707-722.
South America, Brazil
Sao-Luis alluvials
Abstract: Photoluminescence (PL) spectroscopy and electron paramagnetic resonance (EPR) were used for the first time to characterize properties of superdeep diamonds from the São-Luis alluvial deposits (Brazil). The infrared measurements showed the low nitrogen content (>50 of 87 diamonds from this locality were nitrogen free and belonged to type IIa) and simultaneously the extremely high level of nitrogen aggregation (pure type IaB being predominant), which indicates that diamonds under study might have formed under high pressure and temperature conditions. In most cases, PL features excited at various wavelengths (313, 473, and 532 nm) were indicative of different growth and post-growth processes during which PL centers could be formed via interaction between vacancies and nitrogen atoms. The overall presence of the 490.7 nm, H3, and H4 centers in the luminescence spectra attests to strong plastic deformations in these diamonds. The neutral vacancy known as the GR1 center has probably occurred in a number of crystals due to radiation damage in the post-growth period. The 558.5 nm PL center is found to be one of the most common defects in type IIa samples which is accompanied by the EPR center with g-factor of 2.00285. The 536 and 576 nm vibronic systems totally dominated the PL spectra of superdeep diamonds, while none of "normal" diamonds from the Mir pipe (Yakutia) with similar nitrogen characteristics showed the latter three PL centers.
Abstract: Diamond crystals from the Istok (25 crystals) and Mayat (49 crystals) placers were studied using the EPR, IR, and luminescence methods. The total content of impurity nitrogen in forms of A, B, and C (P1) centers ranges from 50 to 1200 ppm. According to the EPR spectroscopy, the presence of nitrogen C (P1), N3V and nitrogen-titanium OK1, N3, NU1 impurity centers was established in the investigated crystals. For 18 crystals from the Istok placer, the N3 nitrogen-titanium center was observed in the EPR spectra, but in the luminescence spectra there was no 440.3 nm system, which was previously attributed to the manifestation of the N3 defect. It is more likely that the nitrogen-titanium N3 EPR center corresponds to the electron-vibrational system 635.7 nm, which is observed in the luminescence spectra of these crystals. Crystals from the Istok placer contain the OK1, N3, and NU1 centers, but luminescence attributed to the oxygen-containing centers is absent in the region of 610-670 nm. For the Mayat placer crystals, the reverse situation was observed. The luminescence ascribed to the oxygen-containing centers was detected for 17 crystals, but there were no OK1, N3, and NU1 centers according to the EPR and luminescence. This result contradicts the arguments of a number of authors about the oxygen nature of these defects. For 5 crystals from the Mayat placer, the nickel impurity was registered. This indicates the presence of ultrabasic paragenesis diamond crystals in this placer.
Physics and Chemistry of Minerals, Vol. 47, 4, 7p. Pdf
Russia, Siberia
deposit - Khololmolokh
Abstract: In recent years, despite significant progress in the development of new methods for the synthesis of diamond crystals and in their post-growth treatment, many questions remain unclear about the conditions for the formation and degradation of aggregate impurity nitrogen forms. Meanwhile, they are very important for understanding (evaluating) the origin, age, and post-growth conditions of natural diamonds. In the present work, an attempt was made to analyze the causes of the formation of high concentrations of N3V centers in natural IaB-type diamonds from the Kholomolokh placer (the Northeast Siberian craton). The possibility of decay of B centers during the plastic deformation of diamonds is analyzed and experiments on the high-temperature annealing of diamonds containing B centers are reported. The formation of N3V centers during the destruction of the B centers at high-pressure annealing of crystals has been established by experiment. It is assumed that, in the post-growth period, diamond crystals were exposed to tectono-thermal stages of raising the superplumes of the Earth's crust of the Siberian craton.
Diamond and Related Materials, Vol. 120, 108638 6p. Pdf
Russia
deposit - Mir
Abstract: In this work, two brownish crystals from the Mir pipe attributed to type IaAB have been examined by a complex of spectroscopic methods: electron paramagnetic resonance, infrared, and photoluminescence spectroscopies. A combination of features such as brownish color, optical system 490.7 nm, and paramagnetic centers W7 and 490.7 points out to plastic deformation of the crystals. The W7 is known to be formed as a result of destruction of A-aggregates during plastic deformation while part of the N3V centrers can be formed due to the disruption of the B-aggregates. The narrow-line EPR spectra from the nitrogen-related N3V centers and the P1 centers indicate that the crystals were annealed after plastic deformation. Another feature of the crystals studied is the observation of the well-known paramagnetic N1 center with only two magnetically inequivalent positions (i.e. with two magnetically inequivalent directions of the C1-N1 fragments) instead of the previously reported four. Possible transformation pathways of the W7 center (N1-C1-C2-N2+) into the N1 center (N1-C-N2+) during the post-deformation annealing are considered.
Abstract: Bridgmanite (Mg,Fe)SiO3, a high pressure silicate with a perovskite structure, is dominant material in the Lower Mantle and therefore is probably the most abundant mineral in the Earth. One single-phase and two composite inclusions of (Mg,Fe)SiO3 coexisting with jeffbenite ((Mg,Fe)3Al2Si3O12), and with jeffbenite and olivine ((Mg,Fe)2SiO4) have been analyzed to identify retrograde phases of former bridgmanite in diamonds from Juina (Brazil). XRD and Raman spectroscopy have revealed that (Mg,Fe)SiO3 inclusions are orthopyroxene at ambient conditions. XRD patterns of these inclusions indicate that they consist of polycrystals. This polycrystalline textures together with high lattice strain of host diamond around these inclusions observed from EBSD may be an evidence for the retrograde phase transition of former bridgmanite. Single-phase inclusions of (Mg,Fe)SiO3 in superdeep diamonds are suggested to represent a retrograde phase of bridgmanite and fully inherit its initial chemical composition, including a high Al and low Ni contents [1,2]. The composite inclusions of (Mg,Fe)SiO3 with jeffbenite and other silicate and oxide phases may be interpreted as exsolution products from originally homogeneous bridgmanite [3]. The bulk compositions of these inclusions are rich in Al, Ti, and Fe which are similar to bridgmanite produced in experiments on the MORB composition. However, the retrograde origin of composite inclusions due to decomposition of Al-rich bridgmanite may be doubtful because each of observed phases may represent single-phase inclusions, i.e. bridgmanite and high pressure garnet (majoritic garnet), with similar compositional features.
South America, Brazil, Africa, South Africa, Guinea, Canada, Northwest Territories
deposit - Sao Luis, Juina
Abstract: Bridgmanite (Mg,Fe)SiO3, a high pressure silicate with a perovskite structure, is dominant material in the lower mantle at the depths from 660 to 2700 km and therefore is probably the most abundant mineral in the Earth. Although synthetic analogues of this mineral have been well studied, no naturally occurring samples had ever been found in a rock on the planet’s surface except in some shocked meteorites. Due to its unstable nature under ambient conditions, this phase undergoes retrograde transformation to a pyroxene-type structure. The identification of the retrograde phase as ‘bridgmanite’ in so-called superdeep diamonds was based on the association with ferropericlase (Mg,Fe)O and other high-pressure (supposedly lower-mantle) minerals predicted from theoretical models and HP-HT experiments. In this study pyroxene inclusions in diamond grains from Juina (Brazil), one single-phase (Sample SL-14) and two composite inclusions of (Mg,Fe)SiO3 coexisting with (Mg,Fe)3Al2Si3O12 (Sample SL-13), and with (Mg,Fe)3Al2Si3O12 and (Mg,Fe)2SiO4 (Sample SL-80) have been analyzed to identify retrograde phases of former bridgmanite. XRD and Raman spectroscopy have revealed that these are orthopyroxene (Opx). (Mg,Fe)2SiO4 and (Mg,Fe)3Al2Si3O12 in these inclusions are identified as olivine and jeffbenite (TAPP). These inclusions are associated with inclusions of (Mg,Fe)O (SL-14), CaSiO3 (SL-80) and composite inclusion of CaSiO3+CaTiO3 (SL-13). XRD patterns of (Mg,Fe)SiO3 inclusions indicate that they consist of polycrystals. This polycrystalline textures together with high lattice strain of host diamond around these inclusions observed from EBSD may be an evidence for the retrograde phase transition of former bridgmanite. Single-phase inclusions of (Mg,Fe)SiO3 in superdeep diamonds are suggested to represent a retrograde phase of bridgmanite and fully inherit its initial chemical composition, including a high Al and low Ni contents [Harte, Hudson, 2013; Kaminsky, 2017]. The composite inclusions of (Mg,Fe)SiO3 with jeffbenite and other silicate and oxide phases may be interpreted as exolusion products from originally homogeneous bridgmanite [Walter et al., 2011]. The bulk compositions of these composite inclusions are rich in Al, Ti, and Fe which are similar to Al-rich bridgmanite produced in experiments on the MORB composition. However, the retrograde origin of composite inclusions due to decomposition of Al-rich bridgmanite may be doubtful because each of observed phases may represent single-phase inclusions, i.e. bridgmanite and high pressure garnet (majoritic garnet), with similar compositional features.
Africa, South Africa, Guinea, Australia,South America, Brazil, Canada, Northwest Territories
deposit - Koffiefontein, Kankan, Lac de Gras, Juina, Machado, Orroroo
Abstract: (Mg,Fe)SiO3 bridgmanite is the dominant phase in the lower mantle; however no naturally occurring samples had ever been found in terrestrial samples as it undergoes retrograde transformation to a pyroxene-type structure. To identify retrograde phases of former bridgmanite single-phase and composite inclusions of (Mg,Fe)SiO3 in a series of superdeep diamonds have been examined with electron microscopy, electron microprobe, Raman spectroscopy and X-ray diffraction techniques. Our study revealed that (Mg,Fe)SiO3 inclusions are represented by orthopyroxene. Orthopyroxenes in single-phase and composite inclusions inherit initial chemical composition of bridgmanites, including a high Al and low Ni contents. In composite inclusions they coexist with jeffbenite (ex-TAPP) and olivine. The bulk compositions of these composite inclusions are rich in Al, Ti, and Fe, which are similar but not fully resembling Al-rich bridgmanite produced in experiments on the MORB composition. The retrograde origin of composite inclusions due to decomposition of Al-rich bridgmanite may be doubtful because each of observed minerals may represent coexisting HP phases, i.e. bridgmanite or ringwoodite.
Angewandte Chemie International edition, Vol. 58, 50, pp. 17918-17929.
Global
nanodiamond
Abstract: Nanodiamond(ND)?based technologies are flourishing in a wide variety of fields spanning from electronics and optics to biomedicine. NDs are considered a family of nanomaterials with an sp3 carbon core and a variety of sizes, shapes, and surfaces. They show interesting physicochemical properties such as hardness, stiffness, and chemical stability. Additionally, they can undergo ad?hoc core and surface functionalization, which tailors them for the desired applications. Noteworthy, the properties of NDs and their surface chemistry are highly dependent on the synthetic method used to prepare them. In this Minireview, we describe the preparation of NDs from the materials?chemistry viewpoint. The different methodologies of synthesis, purification, and surface functionalization as well as biomedical applications are critically discussed. New synthetic approaches as well as limits and obstacles of NDs are presented and analyzed.
Unusually large subsidence and sea-level events during middle Paleozoictime: new evidence supporting mantle convection models for supercontinentassembly
High temperature, high pressure granulites ( retrogressed eclogites) in the central region of the Lewisian NW Scotland: crustal scale subduction in the Neoarchean.
Abstract: The problem of the existence of the asthenosphere for old Precambrian cratons is still discussed. In order to study the seismic lithosphere-asthenosphere boundary (LAB) beneath the Baltic Shield, we used records of nine local earthquakes with magnitudes ranging from 2.7 to 5.9. To model the LAB, original data were corrected for topography and Moho depth using a reference model with a 46-km-thick crust. For two northern events at Spitsbergen and Novaya Zemlya, we observe a low-velocity layer, 60-70-km-thick asthenosphere, and the LAB beneath Barents Sea was found at depth of c. 200 km. Sections for other events show continuous first arrivals of P-waves with no evidence for "shadow zone" in the whole range of registration, which could either be interpreted as the absence of the asthenosphere beneath the central part of the Baltic Shield, or that the LAB in this area occurs deeper (>200 km). The relatively thin low-velocity layer found beneath southern Sweden, 15 km below the Moho, could be interpreted as small-scale lithospheric heterogeneities, rather than asthenosphere. Differentiation of the lower lithosphere velocities beneath the Baltic Shield could be interpreted as regional heterogeneity or as anisotropy of the Baltic Shield lithosphere, with high velocities approximately in the east-west direction, and slow velocities approximately in the south-north direction.
Pure and Applied Geophysics, Vol. 177, 8, pp. 3775-3795. pdf
Europe, Finland
geophysics - seismics
Abstract: The Kokkola-Kymi Deep Seismic Sounding profile crosses the Fennoscandian Shield in northwest-southeast (NW-SE) direction from Bothnian belt to Wiborg rapakivi batholith through Central Finland granitoid complex (CFGC). The 490-km refraction seismic line is perpendicular to the orogenic strike in Central Finland and entirely based on data from quarry blasts and road construction sites in years 2012 and 2013. The campaign resulted in 63 usable seismic record sections. The average perpendicular distance between these and the profile was 14 km. Tomographic velocity models were computed with JIVE3D program. The velocity fields of the tomographic models were used as starting points in the ray tracing modelling. Based on collected seismic sections a layer-cake model was prepared with the ray tracing package SEIS83. Along the profile, upper crust has an average thickness of 22 km average, and P-wave velocities (Vp) of 5.9-6.2 km/s near the surface, increasing downward to 6.25-6.40 km/s. The thickness of middle crust is 14 km below CFGC, 20 km in SE and 25 km in NW, but Vp ranges from 6.6 to 6.9 km/s in all parts. Lower crust has Vp values of 7.35-7.4 km/s and lithospheric mantle 8.2-8.25 km/s. Moho depth is 54 km in NW part, 63 km in the middle and 43 km in SW, yet a 55-km long section in the middle does not reveal an obvious Moho reflection. S-wave velocities vary from 3.4 km/s near the surface to 4.85 km/s in upper mantle, consistently with P-wave velocity variations. Results confirm the previously assumed high-velocity lower crust and depression of Moho in central Finland.
Symposium on critical and strategic materials, British Columbia Geological Survey Paper 2015-3, held Nov. 13-14, pp. 245-250.
Technology
Carbonatite
Abstract: We measured 10 major (SiO2, TiO2, Al2O3, total Fe2O3, MnO, MgO, CaO, Na2O, K2O, and P2O5) and 32 trace (Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Cs, Ba, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Pb, Th, and U) elements in 16 geochemical reference samples (AGV-1, AGV-2, BCR-1, BCR- 2, BHVO-2, BIR-1a, DNC-1a, G-2, GSP-1, GSP-2, MAG-1, QLO-1, RGM-1, RGM-2, SGR-1b, and STM-1) distributed by United States Geological Survey (USGS) and three reference rock samples (SY-2, SY-3, and MRG-1) provided by Canadian Certifi ed Reference Materials Project (CCRMP) using inductively coupled plasma -mass spectrometry coupled with the femtosecond laser ablation sample introduction technique (fsLA-ICP-MS). Before the elemental analysis, fused glassbeads were prepared from the mixture of sample powder and high-purity alkali fl ux with a mixing ratio of 1:10. The abundances of the major and trace elements were externally calibrated by using glass beads containing the major and trace elements prepared from 17 Geological Survey of Japan (GSJ) geochemical reference samples (JB-1, JB-1a, JB-2, JB-3, JA-1, JA-2, JA-3, JR-1, JR-2, JR-3, JP-1, JGb-1, JGb-2, JG-1a, JG- 2, JG-3, and JSy-1). Typical analysis repeatabilities for these geochemical reference samples were better than 3% for Al2O3 and Na2O; <5% for SiO2, TiO2, total Fe2O3, MnO, MgO, CaO, K2O, P2O5, Zn, Rb, Sr, Zr, Nb, Ba, Nd, and U; <8% for Sc, V, Cr, Co, Y, Cs, La, Ce, Pr, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Pb, and Th; <11% for Ni and Cu. These data clearly demonstrate that high analytical repeatability can be achieved by the fsLA-ICP-MS technique with glass beads made from 0.5 g larger samples.
Geochemistry: Exploration, Environment, Analysis, Vol. 19, pp. 414-430.
Canada, British Columbia
geochemistry
Abstract: Using Rock Canyon Creek REE-F-Ba deposit as an example, we demonstrate the need for verifying inherited geochemical data. Inherited La, Ce, Nd, and Sm data obtained by pressed pellet XRF, and La and Y data obtained by aqua regia digestion ICP-AES for 300 drill-core samples analysed in 2009 were compared to sample subsets reanalysed using lithium metaborate-tetraborate (LMB) fusion ICP-MS, Na2O2 fusion ICP-MS, and LMB fusion-XRF. We determine that LMB ICP-MS and Na2O2 ICP-MS accurately determined REE concentrations in SY-2 and SY-4, and provided precision within 10%. Fusion-XRF was precise for La and Nd at concentrations exceeding ten times the lower detection limit; however, accuracy was not established because REE concentrations in SY-4 were below the lower detection limit. Analysis of the sample subset revealed substantial discrepancies for Ce concentrations determined by pressed pellet XRF in comparison to other methods due to Ba interference. Samarium, present in lower concentrations than other REE compared, was underestimated by XRF methods relative to ICP-MS methods. This may be due to Sm concentrations approaching the lower detection limits of XRF methods, elemental interference, or inadequate background corrections. Aqua regia dissolution ICP-AES results, reporting for La and Y, are underestimated relative to other methods.
Prospects of bedrock diamond bearing capacity of the conjugation zone between the Sysolsky anticline and Kirovsk-Kazhimsk aulocogen north of Volga-Urals anteclise.
Doklady Earth Sciences, Vol. 423A, No. 9, pp. 1348-1351.
Physicsa Status Solidi , doi:10.1002/pssa.201900888
Global
HPHT
Abstract: Various samples of multisectoral high?pressure high?temperature (HPHT) single?crystal diamond plate (IIa type) (4?×?4?×?0.53?mm) are tested for particle detection applications. The samples are investigated by X?ray diffractometry, photoluminescence spectroscopy, Raman spectroscopy, Fourier?transform infrared, and visible/ultraviolet (UV) absorption spectroscopy. High crystalline perfection and low impurity concentration (in the {100} growth sector) are observed. To investigate detector parameters, circular 1.0 and 1.5?mm diameter Pt Schottky barrier contacts are created on {111} and {100} growth sectors. On the backside, a Pt contact (3.5?×?3.5?mm) is produced. The {100} growth sector is proved to be a high?quality detector: the full width at half maximum energy resolution is 0.94% for the 5.489?MeV 226Ra ??line at an operational bias of +500?V. Therefore, it is concluded that the HPHT material {100} growth sector is used for radiation detector production, whose quality is not worse than the chemical vapor deposition method or specially selected natural diamond detectors.
Progress in Earth and Planetary Science, Vol. 3, 25, Aug. 22
Mantle
Experimental petrology
Abstract: The Accessible Silicate Earth (ASE) has a higher 142Nd/144Nd ratio than most chondrites. Thus, if the Earth is assumed to have formed from these chondrites, a complement low-142Nd/144Nd reservoir is needed. Such a low-142Nd/144Nd reservoir is believed to have been derived from a melt in the early Earth and is called the Early Enriched Reservoir (EER). Although the major element composition of the EER is crucial for estimating its chemical and physical properties (e.g., density) and is also essential for understanding the origin and fate of the EER, which are both major factors that determine the present composition of the Earth, it has not yet been robustly established. In order to determine the major element composition of the EER, we estimated the age and pressure-temperature conditions to form the EER that would best explain its Nd isotopic characteristics, based on Sm-Nd partitioning and its dependence on pressure, temperature, and melting phase relations. Our estimate indicates that the EER formed within 33.5 Myr of Solar System formation and at near-solidus temperatures and shallow upper-mantle pressures. We then performed high-pressure melting experiments on primitive peridotite to determine the major element composition of the EER at estimated temperature at 7 GPa and calculated the density of the EER. The result of our experiments indicates that the near-solidus melt is iron-rich komatiite. The estimated density of the near-solidus melt is lower than that of the primitive peridotite, suggesting that the EER melt would have ascended in the mantle to form an early crust. Given that high mantle potential temperatures are assumed to have existed in the Hadean, it follows that the EER melt was generated at high pressure and, therefore, its composition would have been picritic to komatiitic. As the formation age of the EER estimated in our study precedes the last giant, lunar-forming impact, the picritic to komatiitic crust (EER) would most likely have been ejected from the Earth by the last giant impact or preceding impacts. Thus, the EER has been lost, leaving the Earth more depleted than its original composition.
Diamond and Related Materials, in press available, 16p.
Technology
Synthetics
Abstract: Diamond synthesis and its morphology by in-liquid plasma chemical vapor deposition (CVD) method are investigated in this study. Diamond films were grown on Si substrates from mixed alcohol solution. Very high growth rate of 170 ?m/h was achieved by this method. Microcrystalline and nanocrystalline diamond films were formed in different conditions. In the case of microcrystalline film, the shapes of diamond grains depend on the location in the film. All morphological differences in this study can be explained by the same mechanism of conventional gas phase CVD method. It means diamond morphology by in-liquid plasma CVD method can be controlled by process parameters as well as gas phase CVD method.
Doklady Earth Sciences, Vol. 465, 1, pp. 1135-1138.
Russia
Deposit - Kimozero
Abstract: Geological and structural mapping of Paleoproterozoic Kimozero kimberlite with account for lithological facies and geochemical specialization provides evidence for the multiphase structure of the kimberlite pipe, which underwent fragmentation as a result of shear–faulting deformations. Two geochemical types of kimberlite (magnesium and carbonate) are distinguished.
Abstract: The paper presents data on the composition of olivine macrocrysts from two Devonian kimberlite pipes in the Arkhangelsk diamond province: the Grib pipe (whose kimberlite belongs to type I) and Pionerskaya pipe (whose kimberlite is of type II, i.e., orangeite). The dominant olivine macrocrysts in kimberlites from the two pipes significantly differ in geochemical and isotopic parameters. Olivine macrocrysts in kimberlite from the Grib pipe are dominated by magnesian (Mg# = 0.92-0.93), Ti-poor (Ti < 70 ppm) olivine possessing low Ti/Na (0.05-0.23), Zr/Nb (0.28-0.80), and Zn/Cu (3-20) ratios and low Li concentrations (1.2-2.0 ppm), and the oxygen isotopic composition of this olivine ?18O = 5.64‰ is higher than that of olivine in mantle peridotites (?18O = 5.18 ± 0.28‰). Olivine macrocrysts in kimberlite from the Pionerskaya pipe are dominated by varieties with broadly varying Mg# = 0.90-0.93, high Ti concentrations (100-300 ppm), high ratios Ti/Na (0.90-2.39), Zr/Nb (0.31-1.96), and Zn/Cu (12-56), elevated Li concentrations (1.9-3.4 ppm), and oxygen isotopic composition ?18O = 5.34‰ corresponding to that of olivine in mantle peridotites. The geochemical and isotopic traits of low-Ti olivine macrocrysts from the Grib pipe are interpreted as evidence that the olivine interacted with carbonate-rich melts/fluids. This conclusion is consistent with the geochemical parameters of model melt in equilibrium with the low-Ti olivine that are similar to those of deep carbonatite melts. Our calculations indicate that the variations in the ?18O of the olivine relative the “mantle range” (toward both higher and lower values) can be fairly significant: from 4 to 7‰ depending on the composition of the carbonate fluid. These variations were formed at interaction with carbonate fluid, whose ?18O values do not extend outside the range typical of mantle carbonates. The geochemical parameters of high-Ti olivine macrocrysts from the Grib pipe suggest that their origin was controlled by the silicate (water-silicate) component. This olivine is characterized by a zoned Ti distribution, with the configuration of this distribution between the cores of the crystals and their outer zones showing that the zoning of the cores and outer zones is independent and was produced during two episodes of reaction interaction between the olivine and melt/fluid. The younger episode (when the outer zone was formed) likely involved interaction with kimberlite melt. The transformation of the composition of the cores during the older episode may have been of metasomatic nature, as follows from the fact that the composition varies from grain to grain. The metasomatic episode most likely occurred shortly before the kimberlite melt was emplaced and was related to the partial melting of pyroxenite source material.
Doklady Earth Sciences, Vol. 482, 1, pp. 1130-1133.
Russia
deposit - Lake Kimozero
Abstract: Syngenetic and epigenetic ore mineralization was studied in Paleoproterozoic metakimberlites in the area of Kimozero Lake. In the Kimozero structure, redeposited ore mineralization is constrained to fracture and shear zones and consists of Fe-vaesite, Fe-Co-polydymite, millerite, Ni-pyrrhotite, pentlandite, chalcopyrite, Zn-bearing copper, galena, and Ni-pyrite. The composition of this mineralization is analogous to that of syngenetic mineralization in pyroclastic and coherent kimberlite, and its likely source was the kimberlite itself.
Abstract: Based on a detailed petrographic investigation and geological observations of the Paleoproterozoic Kimozero kimberlite (Karelia, Russia), we present a new model of kimberlite pipe with multiphase and mono-crater structure. We recognised volcanoclastic and coherent kimberlite series that filled the inner and outer zones of the kimberlite crater. The multiphase structure, emplacement style, petrography and reconstructed size of the Kimozero kimberlite correspond to Phanerozoic kimberlite pipes.
International Journal of Astronomy and Astrophysics, Vol. 1, pp. 98-104.
Asia, Mongolia
astropipes, impact craters
Abstract: In this paper we present summation of eighteen year’s investigation of the all gold and diamond-bearing astropipes of Mongolia. Four astropipe structures are exemplified by the Agit Khangay (10 km in diameter, 470 38' N; 960 05' E), Khuree Mandal (D=11 km; 460 28' N; 980 25' E), Bayan Khuree (D=1 km; 440 06' N; 1090 36' E), and Tsenkher (D=7 km; 980 21' N; 430 36' E) astropipes of Mongolia. Detailed geological and gas-geochemical investigation of the astropipe structures show that diamond genesis is an expression of collision of the lithospheric mantle with the explosion process initiated in an impact collapse meteor crater. The term "astropipes" (Dorjnamjaa et al., 2010, 2011) is a neologism and new scientific discovery in Earth science and these structures are unique in certain aspects. The Mongolian astropipes are genuine "meteorite crater" structures but they also contain kimberlite diamonds and gold. Suevite-like rocks from the astropipes contain such minerals, as olivine, coesite, moissanite (0,6 mm), stishovite, coesite, kamacite,tektite, khamaravaevite (mineral of meteorite titanic carbon), graphite-2H, khondrite, picroilmenite, pyrope, phlogopite, khangaite (tektite glass, 1,0-3,0 mm in size), etc. Most panned samples and hand specimens contain fine diamonds with octahedrol habit (0, 2-2,19 mm, 6,4 mg or 0,034-0,1 carat) and gold (0,1-5 g/t). Of special interest is the large amount of the black magnetic balls (0,05-5,0 mm) are characterized by high content of Ti, Fe, Co, Ni, Cu, Mn, Mg, Cd, Ga, Cl, Al, Si, K. Meanwhile, shatter cones (size approx. 1.0 m) which are known from many meteorite craters on the Earth as being typical of impact craters were first described by us Khuree Mandal and Tsenkher astropipe structures. All the described meteorite craters posses reliable topographic, geological, mineralogical, geochemical, and aerospace mapping data, also some geophysical and petrological features (especially shock metamorphism) have been found, all of which indicate that these structures are a proven new type of gold-diamond-bearing impact structure, termed here "astropipes". The essence of the phenomenon is mantle manifestation and plume of a combined nuclear-magma-palingenesis interaction.
Abstract: HPHT synthesis of diamonds from hydrocarbons attracts great attention due to the opportunity to obtain luminescent nano- and microcrystals of high structure perfection. Systematic investigation of diamond synthesized from the mixture of hetero-hydrocarbons containing dopant elements Si or Ge (C24H20Si and C24H20Ge) with a pure hydrocarbon - adamantane (C10H16) at 8?GPa was performed. The photoluminescence of SiV? and GeV? centers in produced diamonds was found to be saturated when Si and Ge contents in precursors exceed some threshold values. The presence of SiC or Ge as second phases in diamond samples with saturated luminescence indicates that ultimate concentrations of the dopants were reached in diamond. It is shown that SiC inclusions can be captured by growing crystals and be a source of local stresses up to 2?GPa in diamond matrix. No formation of Ge-related inclusions in diamonds was detected, which makes Ge more promising as a dopant in the synthesis method. Surprisingly, the synthesis of diamonds from the C24H20Sn hetero-hydrocarbon was ineffective for SnV? formation: only fluorescence of N-and Si-related color centers was detected at room temperature. As an example of great potential for the synthesis method, mass synthesis of 50-nm diamonds with GeV? centers was realized at 9.4?GPa. Single GeV? production in individual nanodiamond was demonstrated.
Abstract: The paper presents data on the composition of olivine macrocrysts from two Devonian kimberlite pipes in the Arkhangelsk diamond province: the Grib pipe (whose kimberlite belongs to type I) and Pionerskaya pipe (whose kimberlite is of type II, i.e., orangeite). The dominant olivine macrocrysts in kimberlites from the two pipes significantly differ in geochemical and isotopic parameters. Olivine macrocrysts in kimberlite from the Grib pipe are dominated by magnesian (Mg# = 0.92–0.93), Ti-poor (Ti < 70 ppm) olivine possessing low Ti/Na (0.05–0.23), Zr/Nb (0.28–0.80), and Zn/Cu (3–20) ratios and low Li concentrations (1.2–2.0 ppm), and the oxygen isotopic composition of this olivine ?18O = 5.64‰ is higher than that of olivine in mantle peridotites (?18O = 5.18 ± 0.28‰). Olivine macrocrysts in kimberlite from the Pionerskaya pipe are dominated by varieties with broadly varying Mg# = 0.90–0.93, high Ti concentrations (100–300 ppm), high ratios Ti/Na (0.90–2.39), Zr/Nb (0.31–1.96), and Zn/Cu (12–56), elevated Li concentrations (1.9–3.4 ppm), and oxygen isotopic composition ?18O = 5.34‰ corresponding to that of olivine in mantle peridotites. The geochemical and isotopic traits of low-Ti olivine macrocrysts from the Grib pipe are interpreted as evidence that the olivine interacted with carbonate-rich melts/fluids. This conclusion is consistent with the geochemical parameters of model melt in equilibrium with the low-Ti olivine that are similar to those of deep carbonatite melts. Our calculations indicate that the variations in the ?18O of the olivine relative the “mantle range” (toward both higher and lower values) can be fairly significant: from 4 to 7‰ depending on the composition of the carbonate fluid. These variations were formed at interaction with carbonate fluid, whose ?18O values do not extend outside the range typical of mantle carbonates. The geochemical parameters of high-Ti olivine macrocrysts from the Grib pipe suggest that their origin was controlled by the silicate (water–silicate) component. This olivine is characterized by a zoned Ti distribution, with the configuration of this distribution between the cores of the crystals and their outer zones showing that the zoning of the cores and outer zones is independent and was produced during two episodes of reaction interaction between the olivine and melt/fluid. The younger episode (when the outer zone was formed) likely involved interaction with kimberlite melt. The transformation of the composition of the cores during the older episode may have been of metasomatic nature, as follows from the fact that the composition varies from grain to grain. The metasomatic episode most likely occurred shortly before the kimberlite melt was emplaced and was related to the partial melting of pyroxenite source material.
Abstract: South Africa, and attended by representatives of the diamond industry and leaders of African governments to develop a certification process intended to assure that rough, exported diamonds were free of conflictual concerns. This meeting was supported later in 2000 by the United Nations in a resolution adopted by the General Assembly. By 2002, the Kimberley Process Certification Scheme (KPCS) was ratified and signed by diamond-producing and diamond-importing countries. Over 70 countries were included as members of the KPCS at the end of 2007. To prevent trade in "conflict diamonds" while protecting legitimate trade, the KPCS requires that each country set up an internal system of controls to prevent conflict diamonds from entering any imported or exported shipments of rough diamonds. Every diamond or diamond shipment must be accompanied by a Kimberley Process (KP) certificate and be contained in tamper-proof packaging. The objective of this study was (1) to assess the naturally occurring endowment of diamonds in Mali (potential resources) based on geological evidence, previous studies, and recent field data and (2) to assess the diamond-production capacity and measure the intensity of mining activity. Several possible methods can be used to estimate the potential diamond resource. However, because there is generally a lack of sufficient and consistent data recording all diamond mining in Mali and because time to conduct fieldwork and accessibility to the diamond mining areas are limited, four different methodologies were used: the cylindrical calculation of the primary kimberlitic deposits, the surface area methodology, the volume and grade approach, and the content per kilometer approach. Approximately 700,000 carats are estimated to be in the alluvial deposits of the Kenieba region, with 540,000 carats calculated to lie within the concentration grade deposits. Additionally, 580,000 carats are estimated to have been released from the primary kimberlites in the region. Therefore, the total estimated diamond resources in the Kenieba region are thought to be nearly 1,300,000 carats. The Bougouni zones are estimated to have 1,000,000 carats with more than half, 630,000 carats, contained in concentrated deposits. When combined, the Kenieba and Bougouni regions of Mali are estimated to be host to 2,300,000 carats of diamonds.
Journal of Metamorphic Geology, in press available, 44p.
Europe, Bulgaria
Gneiss - diamonds
Abstract: Evidence for ultrahigh-pressure metamorphism (UHPM) in the Rhodope Metamorphic Complex comes from occurrence of diamond in pelitic gneisses, variably overprinted by granulite facies metamorphism, known from several areas of the Rhodopes. However, tectonic setting and timing of UHPM are not interpreted unanimously. Linking age to metamorphic stage is a prerequisite for reconstruction of these processes. Here we use monazite in diamond-bearing gneiss from Chepelare (Bulgaria) to date the diamond-forming UHPM event in the Central Rhodopes. The diamond-bearing gneiss comes from a strongly deformed, lithologically heterogeneous zone (Chepelare Mélange) sandwiched between two migmatized orthogneiss units, known as Arda-I and Arda-II. Diamond, identified by Raman micro-spectroscopy, shows the characteristic band mostly centred between 1332 and 1330 cm?1. The microdiamond occurs as single grains or polyphase diamond + carbonate inclusions, rarely with CO2. Thermodynamic modelling shows that garnet was stable at UHP conditions of 3.5-4.6 GPa and 700-800 °C, in the stability field of diamond, and was re-equilibrated at granulite facies/partial melting conditions of 0.8-1.2 GPa and 750-800 °C. The texture of monazite shows older central parts and extensive younger domains which formed due to metasomatic replacement in solid residue and/or overgrowth in melt domains. The monazite core compositions, with distinctly lower Y, Th and U contents, suggest its formation in equilibrium with garnet. The U-Th-Pb dating of monazite using electron microprobe analysis yielded a c. 200 Ma age for the older cores with low Th, Y, U and high La/Nd ratio, and a c. 160 Ma age for the dominant younger monazite enriched in Th, Y, U and HREE. The older age of around 200 Ma is interpreted as the timing of UHPM whereas the younger age of around 160 Ma as granulite facies/partial melting overprint. Our results suggest that UHPM occurred in Late Triassic to Early Jurassic time, in the framework of collision and subduction of continental crust after the closure of Palaeotethys.
Petrik, I., Janak, M., Froitzheim, N., Georgiev, N., Yoshida, K., Sasinkova, V., Konecny, P., Milovska, S.
Triassic to Early Jurassic ( c. 200Ma) UHP metamorphism in the Central Rhodopes: evidence from U-Pb dating of monazite in diamond bearing gneiss from Chepelare ( Bulgaria).
Journal of Metamorphic Geology, Vol. 34, 3, pp. 265-291.
Petrik, I., Janak, M., Froitzheim, N., Georgiev, N., Yoshida, K., Sasinkova, V., Konecny, P., Milovska, S.
Triassic to Early Jurassic ( c. 200Ma) UHP metamorphism in the central Rhodopes: evidence from U-Pb-Th dating of monazite in diamond bearing gneiss from Chepelare Bulgaria.
Journal of Metamorphic Geology, Vol. 34, 3, pp. 265-291.
Critical evaluation of the status of the areas for future research regarding the wide band GAP semi-conductors diamond, gallium nitride and silicon carbide
Material Sci. Eng. B. Solid State Adv. Technol, Vol. B1, No. 1, Aug. pp. 77-104
Abstract: Despite the advanced stage of diamond thin-film technology, with applications ranging from superconductivity to biosensing, the realization of a stable and atomically thick two-dimensional diamond material, named here as diamondene, is still forthcoming. Adding to the outstanding properties of its bulk and thin-film counterparts, diamondene is predicted to be a ferromagnetic semiconductor with spin polarized bands. Here, we provide spectroscopic evidence for the formation of diamondene by performing Raman spectroscopy of double-layer graphene under high pressure. The results are explained in terms of a breakdown in the Kohn anomaly associated with the finite size of the remaining graphene sites surrounded by the diamondene matrix. Ab initio calculations and molecular dynamics simulations are employed to clarify the mechanism of diamondene formation, which requires two or more layers of graphene subjected to high pressures in the presence of specific chemical groups such as hydroxyl groups or hydrogens.
Earth Planetary Science Letters, Vol. 490, pp. 77-87.
Canada, Ontario
deposit - Victor
Abstract: The central Superior Craton hosts both the diamondiferous 1.1 Ga Kyle Lake and Jurassic Attawapiskat kimberlites. A major thermal event related to the Midcontinent Rift at ca. 1.1 Ga induced an elevated geothermal gradient that largely destroyed an older generation of diamonds, raising the question of when, and how, the diamond inventory beneath Attawapiskat was formed. We determined Re-Os isotope systematics of sulphides included in diamonds from Victor by isotope dilution negative thermal ionisation mass spectrometry in order to obtain insights into the age and nature of the diamond source in the context of regional tectonothermal evolution. Regression of the peridotitic inclusion data (n = 14 of 16) yields a 718 ± 49 Ma age, with an initial 187Os/188Os ratio of 0.1177 ± 0.0016, i.e. depleted at the time of formation (?Os -3.7 ± 1.3). Consequently, Re depletion model ages calculated for these samples are systematically overestimated. Given that reported 187Os/188Os in olivine from Attawapiskat xenoliths varies strongly (0.1012-0.1821), the low and nearly identical initial Os of sulphide inclusions combined with their high 187Re/188Os (median 0.34) suggest metasomatic formation from a mixed source. This was likely facilitated by percolation of amounts of melt sufficient to homogenise Os, (re)crystallise sulphide and (co)precipitate diamond; that is, the sulphide inclusions and their diamond host are synchronous if not syngenetic. The ?720 Ma age corresponds to rifting beyond the northern craton margin during Rodinia break-up. This suggests mobilisation of volatiles (C, N, S) and Os due to attendant mantle stretching and metasomatism by initially oxidising and S-undersaturated melts, which ultimately produced lherzolitic diamonds with high N contents compared to older Kyle Lake diamonds. Thus, some rift-influenced settings are prospective with respect to diamond formation. They are also important sites of hidden, intra-lithospheric volatile redistribution that can be revealed by diamond studies. Later emplacement of the Attawapiskat kimberlites, linking the carbon cycle to the surface, was associated with renewed disturbance during passage of the Great Meteor Hotspot. Lherzolitic diamond formation from oxidising small-volume melts may be the expression of an early and deep stage of the lithospheric conditioning required for the successful eruption of kimberlites, which complements the late and shallow emplacement of volatile-rich metasomes after upward displacement of a redox freezing front.
Bulbuc, K.M., Galarneau, M., Stachel, T., Stern, R.A., Kong, J., Chinn, I.
Contrasting growth conditions for sulphide-and garnet-included diamonds from the Victor mine ( Ontario).
2018 Yellowknife Geoscience Forum , p. 97-98. abstract
Canada, Ontario, Attawapiskat
deposit - Victor
Abstract: The Victor Diamond Mine, located in the Attawapiskat kimberlite field (Superior Craton), is known for its exceptional diamond quality. Here we study the chemical environment of formation of Victor diamonds. We imaged eight sulphide-included diamond plates from Victor using cathodoluminescence (CL). Then, along core-rim transects, we measured nitrogen content and aggregation state utilizing Fourier Transform Infrared (FTIR) spectroscopy, and the stable isotope compositions of carbon (?13C) and nitrogen (?15N), using a multi-collector ion microprobe (MC-SIMS). We compare the internal growth features and chemical characteristics of these sulphide inclusion-bearing diamonds with similar data on garnet inclusion-bearing diamonds from Victor (BSc thesis Galarneau). Using this information, possible fractionation processes during diamond precipitation are considered and inferences on the speciation of the diamond forming fluid(s) are explored. Sulphide inclusion-bearing diamonds show much greater overall complexity in their internal growth features than garnet inclusion-bearing diamonds. Two of the sulphide-included samples have cores that represent an older generation of diamond growth. Compared to garnet inclusion-bearing diamonds, the sulphide-included diamonds show very little intra-sample variation in both carbon and nitrogen isotopic composition; the inter-sample variations in carbon isotopic composition, however, are higher than in garnet included diamonds. For sulphide-included diamonds, ?13C ranges from -3.4 to -17.5 and ?15N ranges from -0.2 to -9.2. Garnet inclusion-bearing diamonds showed ?13C values ranging from -4.6 to -6.0 and ?15N ranging from -2.8 to -10.8. The observation of some 13C depleted samples indicates that, unlike the lherzolitic garnet inclusion-bearing diamonds, the sulphide inclusion-bearing diamonds are likely both peridotitic and eclogitic in origin. The total range in N content across sulphide inclusion-bearing diamonds was 2 to 981 at ppm, similar to the garnet-included samples with a range of 5 to 944 at ppm. The very limited variations in carbon and nitrogen isotopic signatures across growth layers indicate that sulphide-included Victor diamonds grew at comparatively high fluid:rock ratios. This is contrasted by the garnet inclusion-bearing diamonds that commonly show the effects of Rayleigh fractionation and hence grew under fluid-limited conditions.
Canada, Ontario, Attawapiskat, Africa, South Africa
deposit - Victor, Finsch, Newlands
Abstract: Quantitative trace element data from high-purity gem diamonds from the Victor Mine, Ontario, Canada as well as near-gem diamonds from peridotite and eclogite xenoliths from the Finsch and Newlands mines, South Africa, acquired using an off-line laser ablation method show that we see the same spectrum of fluids in both high-purity gem and near-gem diamonds that was previously documented in fibrous diamonds. “Planed” and “ribbed” trace element patterns characterize not only the high-density fluid (HDF) inclusions in fibrous diamonds but also in gem diamonds. Two diamonds from two Finsch harzburgite xenoliths show trace element patterns similar to those of saline fluids, documenting the involvement of saline fluids in the precipitation of gem diamonds, further strengthening the link between the parental fluids of both gem and fibrous diamonds. Differences in trace element characteristics are evident between Victor diamonds containing silicate inclusions compared with Victor diamonds containing sulphide inclusions. The sulphide-bearing diamonds show lower levels of inter-element fractionation and more widely varying siderophile element concentrations - indicating that the silicate and sulphide-bearing diamonds likely formed by gradations of the same processes, via melt-rock reaction or from a subtly different fluid source. The shallow negative LREEN-HREEN slopes displayed by the Victor diamonds establish a signature indicative of original derivation of the diamond forming agent during major melting (~10% melt). Consequently, this signature must have been passed on to HDFs separating from such silicate melts.
Abstract: Quantitative trace element data from high-purity gem diamonds from the Victor Mine, Ontario, Canada as well as near-gem diamonds from peridotite and eclogite xenoliths from the Finsch and Newlands mines, South Africa, acquired using an off-line laser ablation method show that we see the same spectrum of fluids in both high-purity gem and near-gem diamonds that was previously documented in fibrous diamonds. "Planed" and "ribbed" trace element patterns characterize not only the high-density fluid (HDF) inclusions in fibrous diamonds but also in gem diamonds. Two diamonds from two Finsch harzburgite xenoliths show trace element patterns similar to those of saline fluids, documenting the involvement of saline fluids in the precipitation of gem diamonds, further strengthening the link between the parental fluids of both gem and fibrous diamonds. Differences in trace element characteristics are evident between Victor diamonds containing silicate inclusions compared with Victor diamonds containing sulphide inclusions. The sulphide-bearing diamonds show lower levels of inter-element fractionation and more widely varying siderophile element concentrations - indicating that the silicate and sulphide-bearing diamonds likely formed by gradations of the same processes, via melt-rock reaction or from a subtly different fluid source. The shallow negative LREEN-HREEN slopes displayed by the Victor diamonds establish a signature indicative of original derivation of the diamond forming agent during major melting (~10% melt). Consequently, this signature must have been passed on to HDFs separating from such silicate melts.
Abstract: The contribution of magmatic and hydrothermal processes to rare earth element (REE) mineralization of carbonatites remains an area of considerable interest. With the aim of better understanding REE mineralization mechanisms, we conducted a detailed study on the petrology, mineralogy and C-O isotopes of the Bachu carbonatites, NW China. The Bachu carbonatites are composed predominantly of magnesiocarbonatite with minor calciocarbonatite. The two types of carbonatite have primarily holocrystalline textures dominated by dolomite and calcite, respectively. Monazite-(Ce) and bastnäsite-(Ce), the major REE minerals, occur as euhedral grains and interstitial phases in the carbonatites. Melt inclusions in the dolomite partially rehomogenize at temperatures above 800?°C, and those in apatite have homogenization temperatures (Th) ranging from 645 to 785?°C. Oxygen isotope ratios of the calciocarbonatite intrusions (?18OV-SMOW?=?6.4‰ to 8.3‰), similar to the magnesiocarbonatites, indicate the parental magma is mantle-derived, and that they may derive from a more evolved stage of carbonatite fractionation. The magnesiocarbonatites are slightly enriched in LREE whereas calciocarbonatites have higher HREE concentrations. Both dolomite and calcite have low total REE (TREE) contents ranging from 112 to 436?ppm and 88 to 336?ppm, respectively, much lower than the bulk rock composition of the carbonatites (371 to 36,965?ppm). Hence, the fractional crystallization of carbonates is expected to elevate REE concentrations in the residual magma. Rocks from the Bachu deposit with the highest TREE concentration (up to 20?wt%) occur as small size (2?mm to 3 cm) red rare earth-rich veins (RRV) with barite + celestine + fluorapatite + monazite-(Ce) associations. These rocks are interpreted to have a hydrothermal origin, confirmed by the fluid inclusions in barite with Th in the range 198-267?°C. Hydrothermal processes may also explain the existence of interstitial textures in the carbonatites with similar mineral assemblages. The C-O isotopic compositions of the RRV (?13CV-PDB?=??3.6 to ?4.3‰, ?18OV-SMOW?=?7.6 to 9.8‰) are consistent with an origin resulting from fluid exsolution at the end of the high temperature fractionation trend. A two-stage model involving fractional crystallization and hydrothermal fluids is proposed for the mineralization of the Bachu REE deposit.
Abstract: Aillikites are carbonate-rich ultramafic lamprophyres often associated with carbonatites. Despite their common field relationships, the petrogenetic links, if any, between aillikites and carbonatites remain controversial. To address this question, this study reports the results of a detailed geochemical and isotopic examination of the Permian Wajilitag aillikites in the northwestern Tarim large igneous province, including bulk-rock major-, trace-element and Sr-Nd isotope compositions, olivine major- and trace-element and (in-situ secondary ion mass spectrometry) oxygen isotope compositions, oxygen isotope data for clinopyroxene separates, and bulk-carbonate C-O isotopic analyses. Olivine in the aillikites occurs in two textural types: (i) microcrysts, 0.3-5?mm; and (ii) macrocrysts, 0.5-2.5?cm. The microcrysts exhibit well-defined linear correlations between Fo (79-89), minor and trace elements (e.g., Ni?=?1304-3764??g/g and Mn?=?1363-3042??g/g). In contrast, the olivine macrocrysts show low Fo79-81, Ni (5.3-442??g/g) and Ca (477-1018??g/g) and very high Mn (3418-5123??g/g) contents, and are displaced from the compositional trend of the microcrysts. The microcrysts are phenocrysts crystallized from the host aillikite magmas. Conversely, the lack of mantle-derived xenoliths in these aillikites suggests that the macrocrysts probably represent cognate crystals (i.e., antecrysts) that formed from earlier, evolved aillikite melts. Olivine phenocrysts in the more primitive aillikite dykes (Dyke 1) have relatively higher Fo82-89 and mantle-like oxygen isotope values, whereas those in the more evolved dykes (Dyke 2 and 3) exhibit lower Fo79-86 and oxygen isotope values that trend toward lower than mantle ?18O values. The decreasing ?13C values of carbonate from Dyke 1 through to Dyke 2 and 3, coupled with the indistinguishable Sr-Nd isotopes of these dykes, suggest that the low ?18O values of olivine phenocrysts in Dyke 2 and 3 resulted from carbonate melt/fluid exsolution from a common progenitor melt. These lines of evidence combined with the overlapping emplacement ages and Sr-Nd isotope compositions of the aillikites and carbonatites in this area suggest that these exsolved carbonate melts probably contributed to the formation of the Tarim carbonatites thus supporting a close petrogenetic relationship between aillikites and carbonatites.
Abstract: Aillikites are carbonate-rich ultramafic lamprophyres, and although they are volumetrically minor components of large igneous province (LIP), these rocks provide important clues to melting and meta-somatism in the deep mantle domain during the initial stages of LIPs. In this study, we investigate the Wajilitag “kimberlites” in the northwestern part of the Tarim LIP that we redefine as hypabyssal aillikites based on the following features: (1) micro-phenocrystic clinopyroxene and Ti-rich andradite garnet occurring in abundance in the carbonate-rich matrix; (2) Cr-spinel exhibiting typical Fe-Ti enrichment trend also known as titanomagnetite trend; and (3) olivine showing dominantly low Mg values (Fo < 90). To constrain the magma source and evolution, the major, minor, and trace element abundance in olivine grains from these rocks were analyzed using electron microprobe and laser ablation-inductively coupled plasma-mass spectrometry. Olivine in the aillikites occurs as two textural types: (1) groundmass olivines, as sub-rounded grains in matrix, and (2) macrocrysts, as euhedral-anhedral crystals in nodules. The groundmass olivines show varying Mg (Fo89-80) with high-Ni (1606-3418 ppm) and Mn (1424-2860 ppm) and low-Ca (571-896 ppm) contents. In contrast, the macrocrysts exhibit a restricted Fo range but a wide range in Ni and Mn. The former occurs as phenocrysts, whereas the latter are cognate cumulates that formed from earlier, evolved aillikite melt. The two olivine populations can be further divided into sub-groups, indicating a multi-stage crystallization history of the aillikite melt. The crystallization temperatures of groundmass olivines and macrocrysts in dunite nodules as computed from the spinel-olivine thermometers are 1005-1136 and 906-1041 °C, respectively. The coupled enrichment of Ca and Ti and lack of correlation between Ni and Sc and Co in the olivine grains suggest a carbonate-silicate metasomatized mantle source. Moreover, the high 100•Mn/Fe (average 1.67) at high Ni (up to 3418 ppm), overlapping with OIB olivine, and the 100•Ni/Mg (~1) of primitive Mg-Ni-rich groundmass olivines suggest a mixed source that involved phlogopite- and carbonate-rich metasomatic veins within mantle peridotite.
Abstract: Komatiitic magmatism is a characteristic feature of Archean cratons, diagnostic of the addition of juvenile crust, and a clue to the thermal evolution of early Earth lithosphere. The Slave craton in northwest Canada contains >20 greenstone belts but no identified komatiite. The reason for this dearth of komatiite, when compared to other Archean cratons, remains enigmatic. The Central Slave Cover Group (ca. 2.85 Ga) includes fuchsitic quartzite with relict detrital chromite grains in heavy-mineral laminations. Major and platinum group element systematics indicate that the chromites were derived from Al-undepleted komatiitic dunites. The chromites have low 187Os/188Os ratios relative to chondrite with a narrow range of rhenium depletion ages at 3.19 ± 0.12 Ga. While these ages overlap a documented crust formation event, they identify an unrecognized addition of juvenile crust that is not preserved in the bedrock exposures or the zircon isotopic data. The documentation of komatiitic magmatism via detrital chromites indicates a region of thin lithospheric mantle at ca. 3.2 Ga, either within or at the edge of the protocratonic nucleus. This study demonstrates the applicability of detrital chromites in provenance studies, augmenting the record supplied by detrital zircons.
The effects of melt depletion and metasomatism on highly siderophile and strongly chalcophile elements: S-Se-Te-Re-PGE systematics of peridotite xenoliths from Kilbourne Hole, New Mexico.
Geochimica et Cosmochimica Acta, Vol. 166, pp. 210-233.
Journal of the Belarusian State University. Geography and Geology, Title only
Russia
deposit - Vitebsk
Abstract: The article describes the history of studying the diamond content of tectonic structures of the territory of Belarus. Based on the results of magnetometric, mineralogical, tectonic studies carried out by industrial geologists and scientists over the past 50 years, new scientifically substantiated criteria for the search for explosion pipes have been developed using Clifford’s rule, according to which kimberlite explosion pipes are developed within the Archean cratons, where the thickness of the lithosphere is 175–270 km, and are absent in the zones of Early Proterozoic stabilisation and tectonomagmatic activation. Explosion tubes on the African-Arabian, East Siberian, Sino-Korean and East European platforms demonstrate their confinement to the Archean cratons and may be associated with zones of paleosubduction of the Proterozoic oceanic crust beneath the Archean cratons. Based on this, the authors scientifically substantiated the hypothesis that during the closure of the Early Proterozoic paleoocean separating the Fenno-Scandinavian craton from the Volga-Ural and Sarmatian cratons, subduction of the younger crust took place under these cratons, the southwestern corner of which on the territory of Belarus is the Vitebsk granulite massif. The article concludes that the Vitebsk granulite massif is the most promising in terms of diamond-bearing on the territory of Belarus, and within its limits – the Smolensk regional deep fault at the intersection of this fault of northeastern striking with the Odessa-Gomel regional deep fault of submeridional striking south of the city of Orsha. Recommendations are given for further study of promising areas in order to determine their diamond content.
Abstract: The composition of the early Earth’s atmosphere is believed to result from significant magma outgassing during the Archaean eon. It has been widely debated whether the oxygen fugacity (fo2) of the Earth’s mantle has remained constant over the last ~3.8 Ga to levels where volatiles were mostly in their mobile form [1,2], or whether the mantle has experienced a gradual increase of its redox state [3]. Both hypotheses raise fundamental questions on the effect of composition of the early Earth’s accreting material, the origin and availability of primordial carbon in Earth’s interior, and the migration rate of CO2-rich magmas. In addition, the occurrence in nature of carbonatites (or silicate-carbonatitic rocks), diamonds and carbides indicate a dominant control of the mantle redox state on the volatile speciation over time and, maybe, on mechanisms of their formation, reaction and migration through the silicate mantle. A recent model has been developed that combines both experimental results on the fo2 of preserved carbonaceous chondrites at high pressure and thermodynamic predictions of the the temporal variation of the mantle redox state, with the CO2-bearing magmas that could form in the early asthenospheric mantle. Since any variation in melt composition is expected to cause significant changes in the physical properties (e.g., viscosity and density), the migration rate of these magmas has been determined using recent in situ viscosity data on CO2-rich melts with the falling sphere technique. Our results allow determining the composition of CO2- bearing magmas as function of the increasing mantle redox state over time, and the mechanisms and rate for exchange of carbon between mantle reservoirs.
Abstract: Knowledge of the rheology of molten materials at high pressure and temperature is required to understand magma mobility and ascent rate at conditions of the Earth's interior. We determined the viscosity of nominally anhydrous sodium carbonate (Na2CO3), an analogue and ubiquitous component of natural carbonatitic magmas, by the in situ “falling sphere” technique at 1.7, 2.4 and 4.6?GPa, at 1200 to 1700?°C, using the Paris-Edinburgh press. We find that the viscosity of liquid Na2CO3 is between 0.0028?±?0.0001?Pa•s and 0.0073?±?0.0001?Pa•s in the investigated pressure-temperature range. Combination of our results with those from recent experimental studies indicate a negligible dependence on pressure from 1?atm to 4.6?GPa, and a small compositional dependence between molten alkali metal-bearing and alkaline earth metal-bearing carbonates. Based on our results, the viscosity of Na2CO3 is consistent with available viscosity data of both molten calcite (determined at high pressure and temperature) and Na2CO3 at ambient pressure. Molten Na2CO3 is a valid experimental analogue for study of the rheology of natural and/or synthetic near-solidus carbonatitic melts. Estimated values of the mobility and ascent velocity of carbonatitic melts at upper conditions are between 70 and 300?g?cm?3•Pa?1•s?1 and 330-1450?m•year?1, respectively, when using recently proposed densities for carbonatitic melts. The relatively slow migration rate allows magma-rock interaction over time causing seismic anomalies and chemical redox exchange.
Geochemical Perspectives Letters, Vol. 11, pp. 18-22.
Mantle
nitrogen
Abstract: Nitrogen and carbon are essential elements for life, and their relative abundances in planetary bodies are important for understanding planetary evolution and habitability. The high C/N ratio in the bulk silicate Earth (BSE) relative to chondrites has been difficult to explain through partitioning during core formation and outgassing from molten silicate. Here we propose a new model that may have released nitrogen from the metallic cores of accreting bodies during impacts with the early Earth. Experimental observations of melting in the Fe-N-C system via synchrotron X-ray radiography of samples in a Paris-Edinburgh press reveal that above the liquidus, iron-rich melt and nitrogen-rich liquid coexist at pressures up to at least 6 GPa. The combined effects of N-rich supercritical fluid lost to Earth’s atmosphere and/or space as well as N-depleted alloy equilibrating with the magma ocean on its way to the core would increase the BSE C/N ratio to match current estimates.
Minerals MDPI, Vol. 10, 267 doi: 10.23390/min10030267 14p. Pdf
Mantle
Melililite, carbon
Abstract: Understanding the viscosity of mantle-derived magmas is needed to model their migration mechanisms and ascent rate from the source rock to the surface. High pressure-temperature experimental data are now available on the viscosity of synthetic melts, pure carbonatitic to carbonate-silicate compositions, anhydrous basalts, dacites and rhyolites. However, the viscosity of volatile-bearing melilititic melts, among the most plausible carriers of deep carbon, has not been investigated. In this study, we experimentally determined the viscosity of synthetic liquids with ~31 and ~39 wt% SiO2, 1.60 and 1.42 wt% CO2 and 5.7 and 1 wt% H2O, respectively, at pressures from 1 to 4.7 GPa and temperatures between 1265 and 1755 °C, using the falling-sphere technique combined with in situ X-ray radiography. Our results show viscosities between 0.1044 and 2.1221 Pa•s, with a clear dependence on temperature and SiO2 content. The atomic structure of both melt compositions was also determined at high pressure and temperature, using in situ multi-angle energy-dispersive X-ray diffraction supported by ex situ microFTIR and microRaman spectroscopic measurements. Our results yield evidence that the T-T and T-O (T = Si,Al) interatomic distances of ultrabasic melts are higher than those for basaltic melts known from similar recent studies. Based on our experimental data, melilititic melts are expected to migrate at a rate ~from 2 to 57 km•yr?1 in the present-day or the Archaean mantle, respectively.
New dat a on the petrology of olivine lamproites of Western australia From the results of the investigation of magmatic inclusions in olivines.(Russian)
Doklady Academy of Sciences Akademy Nauk SSSR, (Russian), Vol. 284, No. 1, pp. 196-201
Chemical composition, volatile components, and trace elements in melts of the Karymskii volcanic centre, Kamchatka and Golovnin a volcano, Kunashir Island....
Vladykin, N.V., Deep Seated Magmatism: its sources and plumes, pp. 104-127.
Pyrochlore group minerals from Paleozoic carbonatite massifs of the Kola Peninsula: composition and evolution.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 20-21.
Russia, Kola Peninsula
carbonatites
Abstract: Chemical composition and evolution of pyrochlore-group minerals (Nb?Ta?Ti) from the early phoscorites and calcite carbonatites, and late rare-earth dolomite carbonatites from Seblyavr and Vuorijarvi Paleozoic massifs have been studied. There are two trends in pyrochlore composition evolution: the change of U, Ti, and Ta enriched varieties by calcium high-Nb, and the change of early calcium varieties by barium-strontium pyrochlores. The substitutions are described by the typical reactions: 2Ti4+ + U4+ ? 2Nb5+ + Ca2+; Ta5+ ? Nb5+; U4+ + v (vacancy) ? 2Ca2+. The Ca ranges in pyrochlores are explained by isomorphic occupation of the cation position A with Ba, Sr, and REE, the total concentration of which increases as the carbonatite melt evolved and reaches a maximum in rare-earth dolomite carbonatites. The formation of barium pyrochlore is mainly due to successive crystallization from the Ba and Sr enriched melt (oscillatory zoning crystals), or with the secondary replacement of grain margins of the calcium pyrochlore, as an additional mechanism of formation. High enrichments in LREE2O3 (up to 6 wt.%) are identified. The fluorine content in pyrochlore group minerals varies widely. A high concentration (up to 8 wt.%) is found in central and marginal zones of crystals from calcite carbonatites, while it decreases in the pyrochlore from dolomite carbonatites. Fluorine in the crystal lattice has sufficient stability during cation-exchange processes and it is not lost in the case of developing of late carbonatites over the earlier ones. In the late mineral populations the relics enriched by this component are observed. There is a positive correlation of fluorine with sodium. The marginal and fractured zones of pyrochlore crystals from all rock types are represented by phases with a cation deficiency in position A and an increased Si. The evolution of mineral composition depends on the alkaline-ultramafic melt crystallization differentiation, enrichment of the late melts by alkalis and alkaline earth metals at the high fluorine activity. It is determined that the fluorine sharply increases from the early pyroxenites to the carbonatite rocks of the massif. The foscorites and carbonatites of the early stages of crystallization are the most enriched in fluorine, while the late dolomite carbonatites are depleted by this component and enriched in chlorine and water. The fluorine saturation of the early stages of carbonatite melting leads to the formation of fluorapatite and pyrochlore minerals which are the main mineralsconcentrators of fluorine. Pyrochlore group minerals from the Paleozoic carbonatite complexes of the Kola Peninsula are characterized by decreasing Pb, Th and U, and Th/U ratios in the transition from the early foscorites to later calcite carbonatites and hydrothermal dolomite carbonatites. The pyrochlore age varies within the 420-320 m.y. interval (U-Pb SHRIMPII data), while the rocks of the earliest magmatic stages has an individual grain age of 423 ± 15 Ma, but pyrochlore ages for calcite and dolomite carbonatites are younger: 351 ± 8.0 Ma and 324 ± 6.1 Ma, respectively. Such a dispersion of the age data is apparently associated with a disturbed Th/U ratio due to high ability for cation-exchange processes of pyrochlore crystalline matrix including secondary transformations. The research was done within the framework of the scientific program of Russian Academy of Sciences and state contract K41.2014.014 with Sevzapnedra.
Geochemistry International, Vol. 57, 11, pp. 1125-1146.
Russia, Siberia
carbonatite
Abstract: We report the first combined investigation (neutron activation, X-ray fluorescence, and electron microprobe analysis) of mineral forms of Au and Ag and noble metal distribution in the sulfide-bearing phoscorites and carbonatites of the Guli alkaline ultrabasic massif (Polar Siberia) and magnetite and sulfide separates from these rocks. The highest noble metal contents were observed in the sulfide separates from the carbonatites: up to 2.93 Pt, 61.6 Au, and 3.61 ppm Ag. Pyrrhotite, djerfisherite, chalcopyrite, and pyrite are the most abundant sulfides and the main hosts for Au and Ag. The latest assemblage of chalcopyrite, Ag-rich djerfisherite, lenaite, sternbergite, and native silver shows significant Ag concentrations. The wide occurrence of K sulfides and presence of multiphase inclusions in pyrrhotite consisting of rasvumite, K?Na–Ca carbonate, carbocernaite, strontianite, galena, chalcopyrite, sternbergite, lenaite, and native silver suggest that the sulfides were formed at high activities of K, Na, Sr, LREE, F, Cl, and S. Chlorine shows high complex-forming capacity to Ag and could be an agent of noble metal transport in the carbonatites. Crystallization of the early djerfisherite–pyrrhotite assemblages of the phoscorites and carbonatites began at a temperature not lower than 500°C and continued up to the formation of late Ag-bearing sulfides at temperatures not higher than 150°C. The carbonatite-series rocks could be enriched in Au and Ag during late low-temperature stages and serve as a source for Au placers.
Abstract: Mineral zoning in fenites around miaskite intrusions of the Vishnevye Mountains complex can be interpreted as a magmatic-replacement zonal metasomatic aureole (in D.S. Korzhinskii’s understanding): the metasomatic transformations of the fenitized gneisses under the effect of deep alkaline fluid eventually resulted in the derivation of nepheline syenite eutectic melt. Based on the P-T-fO2 parameters calculated from the composition of minerals coexisting in the successive zones, isobaric-isothermal fO2-aSiO2 and µNa2O-µAl2O3 sections were constructed with the Perplex program package to model how the fenites interacted with H2O-CO2 fluid (in the Na-K-Al-Si-Ca-Ti-Fe-Mg-O-H-C system). The results indicate that the fluid-rock interaction mechanisms are different in the outer (fenite) and inner (migmatite) parts of the zonal aureole. Its outer portion was dominated by desilication of rocks, which led, first, to quartz disappearance from these rocks and then to an increase in the Al# of the coexisting minerals (biotite and clinopyroxene). In the inner part of the aureole, fenite transformations into biotite-feldspathic metasomatic rocks and nepheline migmatite were triggered by an increase in the Na and Al activities in the system alkaline H2O-CO2 fluid-rock. As a consequence, the metasomatites were progressively enriched in Al2O3 and alkalis, and these transformations led to the development of biotite in equilibrium with K-Na feldspar and calcite at the sacrifice of pyroxene. The further introduction of alkalis led to the melting of the biotite-feldspathic metasomatites and the origin of nepheline migmatites. The simulated model sequence of metasomatic zones that developed when the gneiss was fenitized and geochemical features of the successive zones (differences in the LILE and REE concentrations in the rocks and minerals of the fenitization aureole and the Sm-Nd isotope systematics of the rocks of the alkaline complex) indicate that the source of the fluid responsible for the origin of zonal fenite-miaskite complexes may have been carbonatite, a derivative of mantle magmas, whereas the miaskites were produced by metasomatic transformations of gneisses and subsequent melting under the effect of fluid derived from carbonatite magmas.
Abstract: Mineral zoning in fenites around miaskite intrusions of the Vishnevye Mountains complex can be interpreted as a magmatic-replacement zonal metasomatic aureole (in D.S. Korzhinskii’s understanding): the metasomatic transformations of the fenitized gneisses under the effect of deep alkaline fluid eventually resulted in the derivation of nepheline syenite eutectic melt. Based on the P-T-fO2 parameters calculated from the composition of minerals coexisting in the successive zones, isobaric-isothermal fO2-aSiO2 and µNa2O-µAl2O3 sections were constructed with the Perplex program package to model how the fenites interacted with H2O-CO2 fluid (in the Na-K-Al-Si-Ca-Ti-Fe-Mg-O-H-C system). The results indicate that the fluid-rock interaction mechanisms are different in the outer (fenite) and inner (migmatite) parts of the zonal aureole. Its outer portion was dominated by desilication of rocks, which led, first, to quartz disappearance from these rocks and then to an increase in the Al# of the coexisting minerals (biotite and clinopyroxene). In the inner part of the aureole, fenite transformations into biotite-feldspathic metasomatic rocks and nepheline migmatite were triggered by an increase in the Na and Al activities in the system alkaline H2O-CO2 fluid-rock. As a consequence, the metasomatites were progressively enriched in Al2O3 and alkalis, and these transformations led to the development of biotite in equilibrium with K-Na feldspar and calcite at the sacrifice of pyroxene. The further introduction of alkalis led to the melting of the biotite-feldspathic metasomatites and the origin of nepheline migmatites. The simulated model sequence of metasomatic zones that developed when the gneiss was fenitized and geochemical features of the successive zones (differences in the LILE and REE concentrations in the rocks and minerals of the fenitization aureole and the Sm-Nd isotope systematics of the rocks of the alkaline complex) indicate that the source of the fluid responsible for the origin of zonal fenite-miaskite complexes may have been carbonatite, a derivative of mantle magmas, whereas the miaskites were produced by metasomatic transformations of gneisses and subsequent melting under the effect of fluid derived from carbonatite magmas.
Cold Regions Science and Technology, Vol. 123, pp. 140-148.
Russia
Geomorphology
Abstract: The paper presents unique results of studying the composition of the ground ice (major components, trace elements, and rare earth elements — REEs) encountered at a depth of 200-250 m in sedimentary and magmatic rocks in the Western Yakutia diamond-bearing regions. In addition to those established earlier, three new geochemical types of ground ice have been defined: (i) sulfate-hydrocarbonate, (ii) chloride-hydrocarbonate, and (iii) sulfate-chloride types with mixed cation composition. The ground ice geochemical features are caused by evolutionary processes of interaction in the water-rock system during permafrost formation. The enclosed rocks were the source for the addition of sulfate and chlorine ions, as well as trace elements, to the ground waters of the active water exchange zone that had existed before freezing. The distribution pattern of REEs in ground ice has a special form distinct from that of sedimentary rocks, kimberlites, and ocean waters, but similar to the REE pattern in local river waters. This REE pattern features the positive europium (Eu) anomaly and approximate equality of light and heavy REEs. The obtained results essentially expand the insight into ice-formation processes in sedimentary and magmatic rocks.
Cold Regions Science and Technology, Vol. 123, pp. 140-148.
Russia, Yakutia
Geomorphology
Abstract: The paper presents unique results of studying the composition of the ground ice (major components, trace elements, and rare earth elements - REEs) encountered at a depth of 200-250 m in sedimentary and magmatic rocks in the Western Yakutia diamond-bearing regions. In addition to those established earlier, three new geochemical types of ground ice have been defined: (i) sulfate-hydrocarbonate, (ii) chloride-hydrocarbonate, and (iii) sulfate-chloride types with mixed cation composition. The ground ice geochemical features are caused by evolutionary processes of interaction in the water-rock system during permafrost formation. The enclosed rocks were the source for the addition of sulfate and chlorine ions, as well as trace elements, to the ground waters of the active water exchange zone that had existed before freezing. The distribution pattern of REEs in ground ice has a special form distinct from that of sedimentary rocks, kimberlites, and ocean waters, but similar to the REE pattern in local river waters. This REE pattern features the positive europium (Eu) anomaly and approximate equality of light and heavy REEs. The obtained results essentially expand the insight into ice-formation processes in sedimentary and magmatic rocks.
International Journal of Earth Sciences, Vol. 106, 8, pp. 1-36.
Africa, Namibia
craton
Abstract: Early Neoproterozoic metaigneous rocks occur in the central part of the Kaoko-Dom Feliciano-Gariep orogenic system along the coasts of the southern Atlantic Ocean. In the Coastal Terrane (Kaoko Belt, Namibia), the bimodal character of the ca. 820-785 Ma magmatic suite and associated sedimentation sourced in the neighbouring pre-Neoproterozoic crust are taken as evidence that the Coastal Terrane formed as the shallow part of a developing back arc/rift. The arc-like chemistry of the bimodal magmas is interpreted as inherited from crustal and/or lithospheric mantle sources that have retained geochemical signature acquired during an older (Mesoproterozoic) subduction-related episode. In contrast, the mantle contribution was small in ca. 800-770 Ma plutonic suites in the Punta del Este Terrane (Dom Feliciano Belt, Uruguay) and in southern Brazil; still, the arc-like geochemistry of the prevalent felsic rocks seems inherited from their crustal sources. The within-plate geochemistry of a subsequent, ca. 740-710 Ma syn-sedimentary volcanism reflects the ongoing crustal stretching and sedimentation on top of the Congo and Kalahari cratons. The Punta del Este-Coastal Terrane is interpreted as an axial part of a Neoproterozoic “Adamastor Rift”. Its opening started in a back-arc position of a long-lasting subduction system at the edge of a continent that fragmented into the Nico Pérez-Luís Alves Terrane and the Congo and Kalahari cratons. The continent had to be facing an open ocean and consequently could not be located in the interior of the Rodinia. Nevertheless, the early opening of the Adamastor Rift coincided with the lifetime of the circum-Rodinia subduction system.
Abstract: The occurrence, morphology, and composition of rinkite are considered against the background of zoning in the Khibiny pluton. Accessory rinkite is mostly characteristic of foyaite in the outer part of pluton, occurs somewhat less frequently in foyaite and rischorrite in the central part of pluton, even more sparsely in foidolites and apatite-nepheline rocks, and sporadically in fenitized xenoliths of the Lovozero Formation. The largest, up to economic, accumulations of rinkite are related to the pegmatite and hydrothermal veins, which occur in nepheline syenite on both sides of the Main foidolite ring. The composition of rinkite varies throughout the pluton. The Ca, Na, and F contents in accessory rinkite and amorphous products of its alteration progressively increase from foyaite and fenitized basalt of the Lovozero Formation to foidolite, rischorrite, apatite-nepheline rocks, and pegmatite-hydrothermal veins.
Abstract: The Kovdor baddeleyite-apatite-magnetite deposit in the Kovdor phoscorite-carbonatite pipe is situated in the western part of the zoned alkali-ultrabasic Kovdor intrusion (NW part of the Fennoscandinavian shield; Murmansk Region, Russia). We describe major intrusive and metasomatic rocks of the pipe and its surroundings using a new classification of phoscorite-carbonatite series rocks, consistent with the IUGS recommendation. The gradual zonation of the pipe corresponds to the sequence of mineral crystallization (forsterite-hydroxylapatite-magnetite-calcite). Crystal morphology, grain size, characteristic inclusions, and composition of the rock-forming and accessory minerals display the same spatial zonation pattern, as do the three minerals of economic interest, i.e. magnetite, hydroxylapatite, and baddeleyite. The content of Sr, rare earth elements (REEs), and Ba in hydroxylapatite tends to increase gradually at the expense of Si, Fe, and Mg from early apatite-forsterite phoscorite (margins of the pipe) through carbonate-free, magnetite-rich phoscorite to carbonate-rich phoscorite and phoscorite-related carbonatite (inner part). Magnetite displays a trend of increasing V and Ca and decreasing Ti, Mn, Si, Cr, Sc, and Zn from the margins to the central part of the pipe; its grain size initially increases from the wall rocks to the inner part and then decreases towards the central part; characteristic inclusions in magnetite are geikielite within the marginal zone of the phoscorite-carbonatite pipe, spinel within the intermediate zone, and ilmenite within the inner zone. The zoning pattern seems to have formed due to both cooling and rapid degassing (pressure drop) of a fluid-rich magmatic column and subsequent pneumatolytic and hydrothermal processes.
Abstract: The comprehensive petrographical, petrochemical and mineralogical study of the Kovdor magnetite-apatite-baddeleyite deposit in the phoscorite-carbonatite complex (Murmansk Region, Russia) revealed a spatial distribution of grain size and chemical composition of three economically extractable minerals — magnetite, apatite, and baddeleyite, showing that zonal distribution of mineral properties mimics both concentric and vertical zonation of the carbonatite-phoscorite pipe. The marginal zone of the pipe consists of (apatite)-forsterite phoscorite carrying fine grains of Ti-Mn-Si-rich magnetite with ilmenite exsolution lamellae, fine grains of Fe-Mg-rich apatite and finest grains of baddeleyite, enriched in Mg, Fe, Si and Mn. The intermediate zone accommodates carbonate-free magnetite-rich phoscorites that carry medium to coarse grains of Mg-Al-rich magnetite with exsolution inclusions of spinel, medium-grained pure apatite and baddeleyite. The axial zone hosts carbonate-rich phoscorites and phoscorite-related carbonatites bearing medium-grained Ti-V-Ca-rich magnetite with exsolution inclusions of geikielite-ilmenite, fine grains of Ba-Sr-Ln-rich apatite and comparatively large grains of baddeleyite, enriched in Hf, Ta, Nb and Sc. The collected data enable us to predict such important mineralogical characteristics of the multicomponent ore as chemical composition and grain size of economic and associated minerals, presence of contaminating inclusions, etc. We have identified potential areas of maximum concentration of such by-products as scandium, niobium and hafnium in baddeleyite and REEs in apatite.
Abstract: The comprehensive petrographical, petrochemical and mineralogical study of the Kovdor magnetite-apatite-baddeleyite deposit in the phoscorite-carbonatite complex (Murmansk Region, Russia) revealed a spatial distribution of grain size and chemical composition of three economically extractable minerals — magnetite, apatite, and baddeleyite, showing that zonal distribution of mineral properties mimics both concentric and vertical zonation of the carbonatite-phoscorite pipe. The marginal zone of the pipe consists of (apatite)-forsterite phoscorite carrying fine grains of Ti-Mn-Si-rich magnetite with ilmenite exsolution lamellae, fine grains of Fe-Mg-rich apatite and finest grains of baddeleyite, enriched in Mg, Fe, Si and Mn. The intermediate zone accommodates carbonate-free magnetite-rich phoscorites that carry medium to coarse grains of Mg-Al-rich magnetite with exsolution inclusions of spinel, medium-grained pure apatite and baddeleyite. The axial zone hosts carbonate-rich phoscorites and phoscorite-related carbonatites bearing medium-grained Ti-V-Ca-rich magnetite with exsolution inclusions of geikielite-ilmenite, fine grains of Ba-Sr-Ln-rich apatite and comparatively large grains of baddeleyite, enriched in Hf, Ta, Nb and Sc. The collected data enable us to predict such important mineralogical characteristics of the multicomponent ore as chemical composition and grain size of economic and associated minerals, presence of contaminating inclusions, etc. We have identified potential areas of maximum concentration of such by-products as scandium, niobium and hafnium in baddeleyite and REEs in apatite.
Abstract: The comprehensive petrographical, petrochemical and mineralogical study of the Kovdor magnetite-apatite-baddeleyite deposit in the phoscorite-carbonatite complex (Murmansk Region, Russia) revealed a spatial distribution of grain size and chemical composition of three economically extractable minerals — magnetite, apatite, and baddeleyite, showing that zonal distribution of mineral properties mimics both concentric and vertical zonation of the carbonatite-phoscorite pipe.The marginal zone of the pipe consists of (apatite)-forsterite phoscorite carrying fine grains of Ti-Mn-Si-rich magnetite with ilmenite exsolution lamellae, fine grains of Fe-Mg-rich apatite and finest grains of baddeleyite, enriched in Mg, Fe, Si and Mn. The intermediate zone accommodates carbonate-free magnetite-rich phoscorites that carry medium to coarse grains of Mg-Al-rich magnetite with exsolution inclusions of spinel, medium-grained pure apatite and baddeleyite. The axial zone hosts carbonate-rich phoscorites and phoscorite-related carbonatites bearing medium-grained Ti-V-Ca-rich magnetite with exsolution inclusions of geikielite-ilmenite, fine grains of Ba-Sr-Ln-rich apatite and comparatively large grains of baddeleyite, enriched in Hf, Ta, Nb and Sc. The collected data enable us to predict such important mineralogical characteristics of the multicomponent ore as chemical composition and grain size of economic and associated minerals, presence of contaminating inclusions, etc. We have identified potential areas of maximum concentration of such by-products as scandium, niobium and hafnium in baddeleyite and REEs in apatite.
Abstract: Hydroxynatropyrochlore, (Na,?a,Ce)2Nb2O6(OH), is a new Na-Nb-OH-dominant member of the pyrochlore supergroup from the Kovdor phoscorite-carbonatite pipe (Kola Peninsula, Russia). It is cubic, Fd-3m, a = 10.3211(3) Å, V = 1099.46 (8) Å3, Z = 8 (from powder diffraction data) or a = 10.3276(5) Å, V = 1101.5(2) Å3, Z = 8 (from single-crystal diffraction data). Hydroxynatropyrochlore is a characteristic accessory mineral of low-carbonate phoscorite of the contact zone of the phoscorite-carbonatite pipe with host foidolite as well as of carbonate-rich phoscorite and carbonatite of the pipe axial zone. It usually forms zonal cubic or cubooctahedral crystals (up to 0.5 mm in diameter) with irregularly shaped relics of amorphous U-Ta-rich hydroxykenopyrochlore inside. Characteristic associated minerals include rockforming calcite, dolomite, forsterite, hydroxylapatite, magnetite,and phlogopite, accessory baddeleyite, baryte, barytocalcite, chalcopyrite, chamosite-clinochlore, galena, gladiusite, juonniite, ilmenite, magnesite, pyrite, pyrrhotite, quintinite, spinel, strontianite, valleriite, and zirconolite. Hydroxynatropyrochlore is pale-brown, with an adamantine to greasy lustre and a white streak. The cleavage is average on {111}, the fracture is conchoidal. Mohs hardness is about 5. In transmitted light, the mineral is light brown, isotropic, n = 2.10(5) (??= 589 nm). The calculated and measured densities are 4.77 and 4.60(5) g•cm-3, respectively. The mean chemical composition determined by electron microprobe is: F 0.05, Na2O 7.97, CaO 10.38, TiO2 4.71, FeO 0.42, Nb2O5 56.44, Ce2O3 3.56, Ta2O5 4.73, ThO2 5.73, UO2 3.66, total 97.65 wt. %. The empirical formula calculated on the basis of Nb+Ta+Ti = 2 apfu is (Na1.02Ca0.73Ce0.09Th0.09 U0.05Fe2+0.02)?2.00 (Nb1.68Ti0.23Ta0.09)?2.00O6.03(OH1.04F0.01)?1.05. The simplified formula is (Na, Ca,Ce)2Nb2O6(OH). The mineral slowly dissolves in hot HCl. The strongest X-ray powderdiffraction lines [listed as (d in Å)(I)(hkl)] are as follows: 5.96(47)(111), 3.110(30)(311), 2.580(100)(222), 2.368(19)(400), 1.9875(6)(333), 1.8257(25)(440) and 1.5561(14)(622). The crystal structure of hydroxynatropyrochlore was refined to R1 = 0.026 on the basis of 1819 unique observed reflections. The mineral belongs to the pyrochlore structure type A2B2O6Y1 with octahedral framework of corner-sharing BO6 octahedra with A cations and OH groups in the interstices. The Raman spectrum of hydroxynatropyrochlore contains characteristic bands of the lattice, BO6, B-O and O-H vibrations and no characteristic bands of the H2O vibrations. Within the Kovdor phoscorite-carbonatite pipe, hydroxynatropyrochlore is the latest hydrothermal mineral of the pyrochlore supergroup, which forms external rims around grains of earlier U-rich hydroxykenopyrochlore and separated crystals in voids of dolomite carbonatite veins. The mineral is named in accordance with the pyrochlore supergroup nomenclature.
Journal of Asian Earth Sciences, in press availabe, 30p.
Asia, Tien Shan
carbonatites
Abstract: Postorogenic intrusions of essexites and alkaline and nepheline syenites in the Turkestan-Alai segment of the Kyrgyz Southern Tien Shan coexist with dikes and veins of carbonatites dated at ?220?Ma by the Ar-Ar and Rb-Sr age methods. They are mainly composed of calcite and dolomite (60-85%), as well as sodic amphibole, phlogopite, clinopyroxene, microcline, albite, apatite, and magnetite, with accessory niobate, ilmenite, Nb-rutile, titanite, zircon, baddeleyite, monazite-(Ce), barite, and sulfides. The rocks share mineralogical and geochemical similarity with carbonatites that originated by liquid immiscibility at high temperatures above 500?°C. Alkaline silicate and salt-carbonate melts are derived from sources with mainly negative bulk ?Nd(t) ? from ?11 to 0 and high initial 87Sr/86Sr ratios (?0.7061-0.7095) which may be due to mixing of PREMA and EM?type mantle material. Pb isotopic ratios in accessory pyrrhotite (206Pb/204Pb?=?18.38; 207Pb/204Pb?=?15.64; 208Pb/204Pb?=?38.41) exhibit an EM2 trend. The intrusions bear signatures of significant crustal contamination as a result of magma genesis by syntexis and hybridism. Concordant isotope composition changes of ?13C (?6.5 to ?1.9‰), ?18O (9.2-23‰), ?D (?58 to ?41‰), and ?34S (12.6-12.8‰) in minerals and rocks indicate inputs of crustal material at the stage of melting and effect of hot fluids released during dehydration of metamorphosed oceanic basalts or sediments. The observed HFSE patterns of the oldest alkaline gabbro may be due to interaction of the primary mafic magma with IAB-type material. The isotope similarity of alkaline rocks with spatially proximal basalts of the Tarim large igneous province does not contradict the evolution of the Turkestan-Alai Triassic magmatism as the “last echo” of the Tarim mantle plume.
Journal of Asian Earth Sciences, Vol. 153, pp. 252-281.
Asia
carbonatite
Abstract: Postorogenic intrusions of essexites and alkaline and nepheline syenites in the Turkestan-Alai segment of the Kyrgyz Southern Tien Shan coexist with dikes and veins of carbonatites dated at ?220?Ma by the Ar-Ar and Rb-Sr age methods. They are mainly composed of calcite and dolomite (60-85%), as well as sodic amphibole, phlogopite, clinopyroxene, microcline, albite, apatite, and magnetite, with accessory niobate, ilmenite, Nb-rutile, titanite, zircon, baddeleyite, monazite-(Ce), barite, and sulfides. The rocks share mineralogical and geochemical similarity with carbonatites that originated by liquid immiscibility at high temperatures above 500?°C. Alkaline silicate and salt-carbonate melts are derived from sources with mainly negative bulk ?Nd(t) ? from ?11 to 0 and high initial 87Sr/86Sr ratios (?0.7061-0.7095) which may be due to mixing of PREMA and EM?type mantle material. Pb isotopic ratios in accessory pyrrhotite (206Pb/204Pb?=?18.38; 207Pb/204Pb?=?15.64; 208Pb/204Pb?=?38.41) exhibit an EM2 trend. The intrusions bear signatures of significant crustal contamination as a result of magma genesis by syntexis and hybridism. Concordant isotope composition changes of ?13C (?6.5 to ?1.9‰), ?18O (9.2-23‰), ?D (?58 to ?41‰), and ?34S (12.6-12.8‰) in minerals and rocks indicate inputs of crustal material at the stage of melting and effect of hot fluids released during dehydration of metamorphosed oceanic basalts or sediments. The observed HFSE patterns of the oldest alkaline gabbro may be due to interaction of the primary mafic magma with IAB-type material. The isotope similarity of alkaline rocks with spatially proximal basalts of the Tarim large igneous province does not contradict the evolution of the Turkestan-Alai Triassic magmatism as the “last echo” of the Tarim mantle plume.
Mineralogy and geochemistry of Triassic carbonatites in the Matcha alkaline intrusive complex ( Turkestan Alai Ridge, Kyrgyz southern Tien Shan), SW central Asian orogenic belt.
Journal of Asian Earth Sciences, Vol. 153, pp. 252-281.
Abstract: This paper reviews the available information on the geology, mineralogy, and resources of the significant rare earth element (REE) deposits and occurrences in the Murmansk Region, northwest Russia. The region has one of the largest endowments of REE in the world, primarily the light REE (LREE); however, most of the deposits are of potential economic interest for the REE, only as by-products of other mining activity, because of the relatively low REE grade. The measured and indicated REE2O3 resources of all deposits in the region total 22.4, and 36.2 million tonnes, respectively. The most important resources occur in (1) the currently mined Khibiny titanite-apatite deposits, and (2) the Lovozero loparite-eudialyte deposit. The Kovdor baddeleyite-apatite-magnetite deposit is a potentially important resource of scandium. These deposits all have polymetallic ores, i.e., REE would be a by-product of P, Ti, and Al mining at Khibiny, Fe, Zr, Ta, and Nb mining at Lovozero, and Fe and Ti mining at Afrikanda. The Keivy block has potential for heavy REE exploitation in the peralkaline granite-hosted Yumperuaiv and Large Pedestal Zr-REE deposits and the nepheline syenite-hosted Sakharyok Zr-REE deposit. With the exception of the Afrikanda perovskite-magnetite deposit (LREE in perovskite) and the Kovdor baddeleyite-apatite-magnetite deposit (scandium in baddelyite), carbonatite-bearing complexes of the Murmansk Region appear to have limited potential for REE by-products. The sound transport, energy, and mining infrastructure of the region are important factors that will help ensure future production of the REE.
Earth and Planetary Science Letters, Vol. 471, pp. 65-73.
Mantle
geochemistry, water cycle
Abstract: Subduction of hydrous and carbonated oceanic lithosphere replenishes the mantle volatile inventory. Substantial uncertainties exist on the magnitudes of the recycled volatile fluxes and it is unclear whether Earth surface reservoirs are undergoing net-loss or net-gain of H2O and CO2. Here, we use noble gases as tracers for deep volatile cycling. Specifically, we construct and apply a kinetic model to estimate the effect of subduction zone metamorphism on the elemental composition of noble gases in amphibole - a common constituent of altered oceanic crust. We show that progressive dehydration of the slab leads to the extraction of noble gases, linking noble gas recycling to H2O. Noble gases are strongly fractionated within hot subduction zones, whereas minimal fractionation occurs along colder subduction geotherms. In the context of our modelling, this implies that the mantle heavy noble gas inventory is dominated by the injection of noble gases through cold subduction zones. For cold subduction zones, we estimate a present-day bulk recycling efficiency, past the depth of amphibole breakdown, of 5-35% and 60-80% for 36Ar and H2O bound within oceanic crust, respectively. Given that hotter subduction dominates over geologic history, this result highlights the importance of cooler subduction zones in regassing the mantle and in affecting the modern volatile budget of Earth's interior.
Abstract: We present Microsoft Excel spreadsheets for calculation of thermodynamic functions and P-V-T properties of MgO, diamond and 9 metals, Al, Cu, Ag, Au, Pt, Nb, Ta, Mo, and W, depending on temperature and volume or temperature and pressure. The spreadsheets include the most common pressure markers used in in situ experiments with diamond anvil cell and multianvil techniques. The calculations are based on the equation of state formalism via the Helmholtz free energy. The program was developed using Visual Basic for Applications in Microsoft Excel and is a time-efficient tool to evaluate volume, pressure and other thermodynamic functions using T-P and T-V data only as input parameters. This application is aimed to solve practical issues of high pressure experiments in geosciences and mineral physics.
Mathematical modeling of the stress strain state in rock and artificial masses during slice chamber mining of underpit reserves in Internationnapa kimberlite.
Journal of Mining Science, Vol. 41, 3, pp. 215-224.
Abstract: Helium isotopes provide an important tool for tracing early-Earth, primordial reservoirs that have survived in the planet’s interior1, 2, 3. Volcanic hotspot lavas, like those erupted at Hawaii and Iceland, can host rare, high 3He/4He isotopic ratios (up to 50 times4 the present atmospheric ratio, Ra) compared to the lower 3He/4He ratios identified in mid-ocean-ridge basalts that form by melting the upper mantle (about 8Ra; ref. 5). A long-standing hypothesis maintains that the high-3He/4He domain resides in the deep mantle6, 7, 8, beneath the upper mantle sampled by mid-ocean-ridge basalts, and that buoyantly upwelling plumes from the deep mantle transport high-3He/4He material to the shallow mantle beneath plume-fed hotspots. One problem with this hypothesis is that, while some hotspots have 3He/4He values ranging from low to high, other hotspots exhibit only low 3He/4He ratios. Here we show that, among hotspots suggested to overlie mantle plumes9, 10, those with the highest maximum 3He/4He ratios have high hotspot buoyancy fluxes and overlie regions with seismic low-velocity anomalies in the upper mantle11, unlike plume-fed hotspots with only low maximum 3He/4He ratios. We interpret the relationships between 3He/4He values, hotspot buoyancy flux, and upper-mantle shear wave velocity to mean that hot plumes—which exhibit seismic low-velocity anomalies at depths of 200 kilometres—are more buoyant and entrain both high-3He/4He and low-3He/4He material. In contrast, cooler, less buoyant plumes do not entrain this high-3He/4He material. This can be explained if the high-3He/4He domain is denser than low-3He/4He mantle components hosted in plumes, and if high-3He/4He material is entrained from the deep mantle only by the hottest, most buoyant plumes12. Such a dense, deep-mantle high-3He/4He domain could remain isolated from the convecting mantle13, 14, which may help to explain the preservation of early Hadean (>4.5 billion years ago) geochemical anomalies in lavas sampling this reservoir1, 2, 3.
Abstract: Mesozoic (125-135 Ma) cratonic low-Ti lamproites from the northern part of the Aldan Shield do not conform to typical classification schemes of ultrapotassic anorogenic rocks. Here we investigate their origins by analyzing olivine and olivine-hosted inclusions from the Ryabinoviy pipe, a well preserved lamproite intrusion within the Aldan Shield. Four types of olivine are identified: (1) zoned phenocrysts, (2) high-Mg, high-Ni homogeneous macrocrysts, (3) high-Ca and low-Ni olivine and (4) mantle xenocrysts. Olivine compositions are comparable to those from the Mediterranean Belt lamproites (Olivine-1 and -2), kamafugites (Olivine-3) and leucitites. Homogenized melt inclusions (MIs) within olivine-1 phenocrysts have lamproitic compositions and are similar to the host rocks, whereas kamafugite-like compositions are obtained for melt inclusions within olivine-3. Estimates of redox conditions indicate that “lamproitic” olivine crystallized from anomalously oxidized magma (?NNO +3 to +4 log units.). Crystallization of "kamafugitic" olivine occurred under even more oxidized conditions, supported by low V/Sc ratios. We consider high-Ca olivine (3) to be a fingerprint of kamafugite-like magmatism, which also occurred during the Mesozoic and slightly preceded lamproitic magmatism. Our preliminary genetic model suggests that low-temperature, extension-triggered melting of mica- and carbonate-rich veined subcontitental lithospheric mantle (SCLM) generated the kamafugite-like melts. This process exhausted carbonate and affected the silicate assemblage of the veins. Subsequent and more extensive melting of the modified SCLM produced volumetrically larger lamproitic magmas. This newly recognized kamafugitic "fingerprint" further highlights similarities between the Aldan Shield potassic province and the Mediterranean Belt, and provides evidence of an overlap between "orogenic" and "anorogenic" varieties of low-Ti potassic magmatism. Moreover, our study also demonstrates that recycled subduction components are not an essential factor in the petrogenesis of low-Ti lamproites, kamafugites and leucitites.
Abstract: 40Ar/39Ar analysis showed a simultaneous (at about 490 Ma) formation of the Paleozoic picrite and basalt complexes of the West Siberian Plate basement. The petrochemistry, trace and REE geochemistry, and composition of clinopyroxene indicate the formation of the picrite of well no. 11 (Chkalov area) as a result of intraplate magmatism of the OIB type. Calculations based on the compositions of clinopyroxene allowed crystallization of minerals of porphyric picrite at 1215-1275°C and 4.5-8 kbar. In general, it has been found that the picrite basalt complexes considered were formed from enriched igneous plume systems under intraplate conditions near the active margin of the ancient ocean.
Phase relations and stability of magnetoplumbite and crichtonite series phases under upper mantle P-T conditions: an experimental study to 15 GPa with LILE
Phase relations and stability of magnetoplumbite and crichtonite series phases under upper mantle P T conditions: an experimental study to 15 GPa. LILE
The high PT stability of apatite and Cl partioning between apatite and hydrous potassic phases in peridotite: an experimental study to 19 Gpa with implcations for the transport of P, Cl, and K in the upper mantle.
Contributions to Mineralogy and Petrology, Vol. 163, 2, pp. 277-296.
Konzett, J., Wirth, R., Hauzenberger, C., Whitehouse, M.
Two episodes of fluid migration in the Kaapvaal Craton lithospheric mantle associated with Cretaceous kimberlite activity: evidence from a harzburgite containing a unique assemblage of metasomatic zirconium-phases.
Earth and Planetary Science Letters, Vol. 465, pp. 59-69.
Mantle
Geothermometry
Abstract: Crustal foundering is an important mechanism in the differentiation and recycling of continental crust. Nevertheless, little is known about the dynamics of the lower crust, the temporal scale of foundering and its role in the dynamics of active margins and orogens. This particularly applies to active settings where the lower crust is typically still buried and direct access is not possible. Crustal xenoliths derived from mantle depth in the Pamir provide a unique exception to this. The rocks are well-preserved and comprise a diverse set of lithologies, many of which re-equilibrated at high-pressure conditions before being erupted in their ultrapotassic host lavas. In this study, we explore the petrological and chronological record of eclogite and felsic granulite xenoliths. We utilized accessory minerals - zircon, monazite and rutile - for coupled in-situ trace-element analysis and U-(Th-)Pb chronology by laser-ablation (split-stream) inductively coupled plasma mass spectrometry. Each integrated analysis was done on single mineral zones and was performed in-situ in thin section to maintain textural context and the ability to interpret the data in this framework. Rutile thermo-chronology exclusively reflects eruption (View the MathML source11.17±0.06Ma), which demonstrates the reliability of the U-Pb rutile thermo-chronometer and its ability to date magmatic processes. Conversely, zircon and monazite reveal a series of discrete age clusters between 55-11 Ma, with the youngest being identical to the age of eruption. Matching age populations between samples, despite a lack of overlapping ages for different chronometers within samples, exhibit the effectiveness of our multi-mineral approach. The REE systematics and age data for zircon and monazite, and Ti-in-zircon data together track the history of the rocks at a million-year resolution. The data reveal that the rocks resided at 30-40 km depth along a stable continental geotherm at 720-750?°C until 24-20 Ma, and were subsequently melted, densified, and buried to 80-90 km depth - 20 km deeper than the present-day Moho - at View the MathML source930±35°C. The material descended rapidly, accelerating from 0.9-1.7 mm?yr?1 to 4.7-5.8 mm?yr?1 within 10-12 Myr, and continued descending after reaching mantle depth at 14-13 Ma. The data reflect the foundering of differentiated deep-crustal fragments (2.9-3.5 g?cm?3) into a metasomatized and less dense mantle wedge. Through our new approach in constraining the burial history of rocks, we provided the first time-resolved record of this crustal-recycling process. Foundering introduced vestiges of old evolved crust into the mantle wedge over a relatively short period (c. 10 Myr). The recycling process could explain the variability in the degree of crustal contamination of mantle-derived magmatic rocks in the Pamir and neighboring Tibet during the Cenozoic without requiring a change in plate dynamics or source region.
Abstract: The burial and exhumation of continental crust during collisional orogeny exert a strong control on the dynamics of mountain belts and plateaus. Constraining the rates and style of exhumation of deeply buried crust has proven difficult due to complexities in the local geology and thermochronometric methods typically used. To advance this field, we applied trace?element and U?Pb laser ablation inductively coupled plasma mass spectrometry analyses to rutile from eclogite and amphibolite samples from the Western Gneiss Complex of Norway—an archetypal continental (ultra)high?pressure (UHP) terrane. Peak temperature and timing of midcrustal cooling were constrained for samples collected along a subduction? and exhumation?parallel transect, using Zr?in?rutile thermometry and U?Pb rutile geochronology, respectively. Peak temperatures decrease from 830 °C in the UHP domain to 730 °C at the UHP?HP transition, remain constant at 730 °C across most of the terrane, and decrease to 620 °C at the eclogite?out boundary. U?Pb results show that most of the terrane cooled through 500 °C at 380-375 Ma except for the lowest grade region, where cooling occurred approximately 20 million years earlier. The results indicate that exhumation was a two stage process, involving (1) flexural rebound and slab flattening at depth combined with foreland?directed extrusion, followed by (2) synchronous cooling below 500 °C across the, by then, largely flat?lying Western Gneiss Complex. The latter implies and requires relatively homogeneous mass removal across a large area, consistent with erosion of an overlying orogenic plateau. The Caledonides were at near?equatorial latitudes at the time. A Caledonian paleo?plateau thus may represent a so far unrecognized factor in Devonian and Carboniferous atmospheric circulation and climate forcing.
Abstract: The first find of microdiamond in the Nordøyane ultra-high-pressure (UHP) domain of the Western Gneiss Region (WGR) of the Scandinavian Caledonides reshaped tectonic models for the region. Nevertheless, in spite of much progress regarding the meaning and significance of this find, the history of rock that the diamonds were found in is complex and still largely ambiguous. To investigate this, we report U-Pb zircon ages obtained from the exact crushed sample material in which metamorphic diamond was first found. The grains exhibit complicated internal zoning with distinct detrital cores overgrown by metamorphic rims. The cores yielded a range of ages from the Archaean to the late Neoproterozoic / early Cambrian. This detrital zircon age spectrum is broadly similar to detrital signatures recorded by metasedimentary rocks of the Lower and Middle allochthons elsewhere within the orogen. Thus, our dating results support the previously proposed affinity of the studied gneiss to the Seve-Blåhø Nappe of the Middle Allochthon. Metamorphic rims yielded a well-defined peak at 447 ± 2 Ma and a broad population that ranges between c. 437 and 423 Ma. The data reveal a prolonged metamorphic history of the Fjørtoft gneiss that is far more complex then would be expected for a UHP rock that has seen a single burial and exhumation cycle. The data are consistent with a model involving multiple such cycles, which would provide renewed support for the dunk tectonics model that has been postulated for the region.
Earth and Planetary Science letters, Vol. 528, 115820 11p.
Mantle
craton
Abstract: The continental crust and sub-continental lithospheric mantle (SCLM) are co-dependent reservoirs in terms of their geochemistry, tectonics, and long-term evolution. Obtaining insight into the mechanisms of lithosphere formation and differentiation requires robust constraint on the complex petrological history of mantle rocks. This has proven difficult as samples from the deep mantle are rare and, although many may have formed in the Archean, no such age has been obtained directly from mantle-derived silicate minerals. Lutetium-hafnium geochronology of garnet has the potential of overcoming this limitation. In this study, this technique was applied on fragments of the SCLM exposed in the Norwegian Caledonides. The chronologic record of these rocks is rich and extensive, yet it is difficult to interpret and is, in part, inconsistent. Our Lu-Hf results from supersilicic pyrope in dunite provide the first Archean internal isochron ages for mantle rocks. These ages are consistent with a period of juvenile crust formation worldwide and provide a record of deeply sourced mantle upwellings from >350 km depth. Results from fertile rock types indicate that melting and isotope re-equilibration occurred in sync with two Proterozoic supercontinent break-up events that are recorded in the Laurentian and Baltic lithospheres. Together, the results indicate that since its extraction during a period of rapid Archean crustal growth, the SCLM appears to have largely been at petro-physical and chemical stasis, with the exception of major episodes of continental break-up. The evolution of the SCLM is thus, highly punctuated and ultimately controlled by the Wilson cycle.
Americam Geophysical Union Fall meeting, 1p. Abstract
Europe, Norway
eclogites, peridotites
Abstract: The preservation of Archean cratons is typically attributed to the presence of a highly-depleted and buoyant sub-continental lithospheric mantle (SCLM) that is equally old or older than its overlying crust. Time constraints on the formation and petrological evolution of the SCLM are key to investigating its long-term evolution and role in the formation and preservation of the continental crust. Nevertheless, such constraints are difficult to obtain as well-preserved samples of the SCLM are rare and typically lack conventional chronometric minerals. The history of SCLM rocks is typically inferred on the basis of model ages, many of which indicate an Archean origin; however, these dates are difficult to link to specific mineral assemblages or chemical signatures, and the petrological and dynamic processes that these represent. Garnet Lu-Hf geochronology is one of the few chronometers that could overcome this limitation. In this study, a refined method in Lu-Hf garnet chronology was applied to fragments of the Laurentian SCLM that are now exposed as orogenic peridotites in the ultrahigh-pressure domains of the Western Gneiss Complex, Norway. The peridotite bodies comprise a variety of unusually well-preserved rock types-from dunites that record decompression and melting at >350 km depth to fertile lithologies produced by melting and fluid metasomatism. Our internal isochron results from pyrope (after exsolution from majorite) in dunite samples yielded identical Neoarchean ages; these are the first-ever obtained for mantle garnet. The ages coincide with a time interval during which there was voluminous juvenile crust formation, indicating a link between this global process and the deeply sourced mantle upwellings that these samples represent. Internal isochrons from websterite-and clinopyroxenite-hosted pyrope yielded Meso-to Neoproterozoic ages that exactly match two distinct supercontinent break-up events in the overlying continental crust. Together, the new Lu-Hf results indicate that since its extraction during a period of widespread Archean crustal growth, the Laurentian SCLM appears to have largely been at petro-physical and chemical stasis and evolved only during short pulses that ran in sync with the supercontinent cycle.
American Geophysical Union, Fall Meeting. , V23A-05 1p.
Mantle
geophysics
Abstract: Variations in radiogenic isotopes in mid-ocean ridge basalts (MORB) are interpreted to reflect the presence of enriched and depleted mantle components in their source regions and have been used to infer the abundance and time scales of crustal recycling. However, MORB are homogenized via magma mixing prior to eruption and may not capture the full heterogeneity of melts generated in their upper mantle source. Here we show that primitive cumulate minerals, formed by crystallization of mantle melts in the lower crust, retain the signature of the recycled material. We performed high spatial resolution Nd and Sr isotopic analyses on clinopyroxene and plagioclase of gabbroic cumulates from the Atlantis massif, located on a depleted ridge segment on the northern Mid-Atlantic Ridge, and compared these data with whole rock isotopic compositions of diabase and microgabbros collected on the same core, associated basalts flows, and MORB data from the literature. We find that cumulate minerals: (1) are significantly more isotopically heterogeneous than the associated diabase and lavas, exceeding the range of 143Nd/144Nd in MORB by a factor of seven; and (2) contain the full Nd isotopic heterogeneity of all of North Atlantic MORB. Furthermore, we find that isotopic heterogeneity occurs down to the sample scale, with plagioclase and clinopyroxene from individual samples commonly not in isotopic equilibrium. We further demonstrate that the MORB and cumulate mineral data can be reconciled with constant high magnitude, small length scale heterogeneity through the North Atlantic upper mantle, with limited magma mixing in the mantle and extensive mixing in the oceanic crust.The isotopic heterogeneity revealed in the lower oceanic crust provides strong evidence that MORB is not an accurate representation of the heterogeneity of its mantle source. Hence, the true isotopic variation of the upper mantle requires rigorous further examination, and models of convective thinning and stretching and melt migration must be re-evaluated to account for greater local variation.
Geochimica et Cosmochimica Acta, 10.1016/j.gca.2020.10.010 35p. Pdf
Africa, Botswana
deposit - Jwaneng
Abstract: Constraining the formation age of individual diamonds from incorporated mineral inclusions and assessing the host diamonds’ geochemical characteristics allows determination of the complex history of diamond growth in the sub-continental lithospheric mantle (SCLM). It also provides the rare opportunity to study the evolution of the deep cycling of volatiles over time. To achieve these aims, Sm-Nd isotope systematics are presented for 36 eclogitic garnet and clinopyroxene inclusions from 16 diamonds from the Jwaneng mine, Botswana. The inclusions and host diamonds comprise at least two compositional suites that record different ‘mechanisms’ of diamond formation and define two isochrons, one Paleoproterozoic (1.8 Ga) and one Neoproterozoic (0.85 Ga). There are indications of at least three additional diamond-forming events whose ages currently cannot be well constrained. The Paleoproterozoic diamond suite formed by large-scale (> 100’s km), volatile-rich metasomatism related to formation and re-working of the Proto-Kalahari Craton. In contrast, the heterogeneous composition of the Neoproterozoic diamond suite indicates diamond formation on a small-scale, through local (< 10 km) equilibration of compositionally variable diamond-forming fluids in different eclogitic substrates during the progressive breakup of the Rodinia supercontinent. The results demonstrate that regional events appear to reflect the input of volatiles (i.e., carbon-bearing) derived from the asthenospheric mantle, whereas local diamond-forming events mainly promote the redistribution of volatiles within the SCLM. The occurrence of isotopically light carbon analysed in distinct growth zones from samples of this study (?13C < -21.1‰) provides further indication of a recycled origin for surface-derived carbon in some diamonds from Jwaneng. Determining Earth’s long-term deep carbon cycle using diamonds, however, requires an understanding of the nature and scale of specific diamond-forming events.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 5540 Abstract
Africa, Botswana
Deposit - Letlhakane
Abstract: The diamondiferous Letlhakane kimberlites are part of the Orapa kimberlite cluster (˜ 93.1 Ma) in north-eastern Botswana, located on the edge of the Zimbabwe Craton, close to the Proterozoic Magondi Mobile Belt. Here we report the first Re-Os ages of six individual eclogitic sulphide inclusions (3.0 to 35.7?g) from Letlhakane diamonds along with their rhenium, osmium, iridium and platinum concentrations, and carbon isotope, nitrogen content and N-aggregation data from the corresponding growth zones of the host diamonds. For the first time, Re-Os data will be compared to Sm-Nd ages of individual eclogitic silicate inclusions recovered from the same diamonds using a Triton Plus equipped with four 1013? amplifiers. The analysed inclusion set currently encompasses pairs of individual sulphides from two diamonds (LK040 sf4 & 5, LK113 sf1 & 2) and two sulphide inclusions from separate diamonds (LK048, LK362). Ongoing work will determine the Sm-Nd ages and element composition of multiple individual eclogitic garnets (LK113/LK362, n=4) and an eclogitic clinopyroxene (LK040) inclusion. TMA ages of the six sulphides range from 1.06 to 2.38 Ga (± 0.1 to 0.54 Ga) with Re and Os contents between 7 and 68 ppb and 0.03 and 0.3 ppb, respectively. The host diamond growth zones have low nitrogen abundances (21 to 43 ppm N) and high N-aggregation (53 to 90% IaB). Carbon isotope data suggests the involvement of crustal carbon (?13C between -19.3 to -22.7 ± 0.2 per mill) during diamond precipitation. Cathodoluminescence imaging of central plates from LK040 and LK113 displays homogenous internal structure with no distinct zonation. The two sulphide inclusions from LK040 define an 'isochron' of 0.92 ± 0.23 Ga (2SD) with initial 187Os/188Os = 1.31 ± 0.24. Sulphides from LK113 have clear imposed diamond morphology and indicate diamond formation at 0.93 ± 0.36 Ga (2SD) with initial 187Os/188Os = 0.69 ± 0.44. The variation in the initial 187Os/188Os does not justify including these inclusions (or any from other diamonds) on the same isochron and implies an extremely heterogeneous diamond crystallisation environment that incorporated recycled Os. C1-normalized osmium, iridium and platinum (PGE) compositions from the analysed sulphide inclusions display enrichment in Ir (3.4 to 33) and Pt (2.3 to 28.1) in comparison to eclogitic xenolith data from Orapa that are depleted relative to chondrite. The Re-Os isochrons determined in this study are within error of previously reported ages from the adjacent (˜40km) Orapa diamond mine (1.0 to 2.9 Ga) based on sulphide inclusions and a multi-point 990 ± 50 Ma (2SD) isochron for composite (n=730) silicate inclusions. Together with additional new Sm-Nd isochron age determinations from individual silicate inclusions from Letlhakane (2.3 ± 0.02 (n = 3); 1.0 ± 0.14 (n = 4) and 0.25 ± 0.04 Ga (n = 3), all 2SE) these data suggest a phase of Mesoproterozoic diamond formation as well as Neoarchean/Paleoproterozoic and Mesozoic diamond growth, in punctuated events spanning >2.0 Ga.
Earth and Planetary Science Letters, Vol. 463, pp. 178-188.
Africa, Botswana
Deposit - Lethakane
Abstract: Monocrystalline diamonds commonly record complex internal structures reflecting episodic growth linked to changing carbon-bearing fluids in the mantle. Using diamonds to trace the evolution of the deep carbon cycle therefore requires dating of individual diamond growth zones. To this end Rb-Sr and Sm-Nd isotope data are presented from individual eclogitic silicate inclusions from the Orapa and Letlhakane diamond mines, Botswana. ?13C?13C values are reported from the host diamond growth zones. Heterogeneous 87Sr/86Sr ratios (0.7033-0.7097) suggest inclusion formation in multiple and distinct tectono-magmatic environments. Sm-Nd isochron ages were determined based on groups of inclusions with similar trace element chemistry, Sr isotope ratios, and nitrogen aggregation of the host diamond growth zone. Diamond growth events at 0.14±0.090.14±0.09, 0.25±0.040.25±0.04, 1.1±0.091.1±0.09, 1.70±0.341.70±0.34 and 2.33±0.022.33±0.02 Ga can be directly related to regional tectono-magmatic events. Individual diamonds record episodic growth with age differences of up to 2 Ga. Dated diamond zones have variable ?13C?13C values (?5.0 to ?33.6‰ vs PDB) and appear to imply changes in subducted material over time. The studied Botswanan diamonds are interpreted to have formed in different tectono-magmatic environments that involve mixing of carbon from three sources that represent: i) subducted biogenic sediments (lightest ?13C?13C, low 87Sr/86Sr); ii) subducted carbonate-rich sediments (heavy ?13C?13C, high 87Sr/86Sr) and iii) depleted upper mantle (heavy ?13C?13C, low 87Sr/86Sr). We infer that older diamonds from these two localities are more likely to have light ?13C?13C due to greater subduction of biogenic sediments that may be related to hotter and more reduced conditions in the Archaean before the Great Oxidation Event at 2.3 Ga. These findings imply a marked temporal change in the nature of subducted carbon beneath Botswana and warrant further study to establish if this is a global phenomenon.
Abstract: Precise dating of diamond growth is required to understand the interior workings of the early Earth and the deep carbon cycle. Here we report Sm-Nd isotope data from 26 individual garnet inclusions from 26 harzburgitic diamonds from Venetia, South Africa. Garnet inclusions and host diamonds comprise two compositional suites formed under markedly different conditions and define two isochrons, one Archaean (2.95?Ga) and one Proterozoic (1.15?Ga). The Archaean diamond suite formed from relatively cool fluid-dominated metasomatism during rifting of the southern shelf of the Zimbabwe Craton. The 1.8 billion years younger Proterozoic diamond suite formed by melt-dominated metasomatism related to the 1.1?Ga Umkondo Large Igneous Province. The results demonstrate that resolving the time of diamond growth events requires dating of individual inclusions, and that there was a major change in the magmatic processes responsible for harzburgitic diamond formation beneath Venetia from the Archaean to the Proterozoic.
Geophysical Research Abstracts www.researchgate.net, Vol. 20, EGU2018-128291p. Abstract
Africa, South Africa
diamond inclusions
Abstract: Changing recycling budgets of surface materials and volatiles by subduction of tectonic plates influence the compositions of Earth’s major reservoirs and affect climate throughout geological time. Fluids play a key role in processes governing subduction recycling, but quantifying the exact fate of volatiles introduced into the mantle at ancient and recent destructive plate boundaries remains difficult. Here, we report on the role of fluids and the fate of volatiles and other elements at two very different tectonic settings: 1) at subduction settings, and 2) within the subcontinental lithospheric mantle (SCLM). We will show how olivine-hosted melt inclusions from subduction zones and mineral inclusions in diamond from the SCLM are used to reveal how changing tectonic settings influence volatile cycles with time. Melt inclusions from the complex Italian post-collisional tectonic setting are used to identify changing subduction recycling through time. The use of CO2 in deeply trapped melt inclusions instead of in lavas or volcanic gases provides a direct estimate of deep recycling, minimizing possible effects of contamination during transfer through the crust. The aim is to distinguish if increased recycling of sediments from the down-going plate at continental subduction settings results in increased deep CO2 recycling or if the increased CO2 flux results from crustal degassing of the overriding plate. Both processes likely affected climate through Earth history but could thus far not be discriminated. The study of mineral inclusions and their host diamonds from the SCLM can link changes in the cycling of carbon-rich fluids and the time and process through which the carbon redistribution took place. We use Sm-Nd isotope techniques to date the mineral inclusions and use the carbon isotope data of the host diamonds to investigate the growth conditions. I will present case-studies of peridotitic and eclogitic diamonds from three mines in Southern Africa.
Abstract: The diamondiferous Jwaneng kimberlite cluster (~240 Ma) is located on the NW rim of the Archaean Kaapvaal Craton in central Botswana. Previous studies report eclogitic diamond formation in the late Archean (2.9 Ga) and in the Middle Proterozoic (1.5 Ga) involving different mantle and sedimentary components [1;2;3]. Here we report newly acquired Sm- Nd ages of individual eclogitic pyrope-almandine and omphacite inclusions along with their major element data and nitrogen data from the diamond hosts to re-examine Jwaneng’s diamond formation ages. The Sm-Nd isotope analyses were performed via TIMS using 1013? resistors [4]. An initial suite of three pyropealmandine and 14 omphacite inclusions yield 143Nd/144Nd from 0.51102±7 to 0.5155±5. 147Sm/144Nd vary from 0.024 to 0.469. Major element data defines two inclusion populations: (1) seven omphacites with high Mg#, high Cr# and one pyropealmandine with low-Ca define an isochron age of 1.93±0.16 Ga with ?Ndi= +3.5; (2) seven omphacites with low Mg#, low Cr# and two pyrope-almandines with low-Ca define an isochron age of 0.82±0.06 Ga with ?Ndi= +3.7. Nitrogen contents of corresponding diamond host growth zones in Group (1) are ? 50 at.ppm whereas Group (2) range between 50 to 700 at.ppm with N-aggregation > 70 %B. Additional data used to define “co-genetic” inclusion suites include Sr-isotopes and trace elements of the inclusions and carbon isotopes of the diamond hosts. Re-Os data of coexisting sulphide inclusions from the same silicate-bearing diamonds further validates the ages and indicates more periods of diamond formation at Jwaneng than previously assumed. The integrated data indicate the possibility of an extensive Paleoproterozoic diamond-forming event in southern Africa.
Abstract: The Earth’s mantle is heterogeneous as a result of early planetary differentiation and subsequent crustal recycling during plate tectonics. Radiogenic isotope signatures of mid-ocean ridge basalts have been used for decades to map mantle composition, defining the depleted mantle endmember. These lavas, however, homogenize via magma mixing and may not capture the full chemical variability of their mantle source. Here, we show that the depleted mantle is significantly more heterogeneous than previously inferred from the compositions of lavas at the surface, extending to highly enriched compositions. We perform high-spatial-resolution isotopic analyses on clinopyroxene and plagioclase from lower crustal gabbros drilled on a depleted ridge segment of the northern Mid-Atlantic Ridge. These primitive cumulate minerals record nearly the full heterogeneity observed along the northern Mid-Atlantic Ridge, including hotspots. Our results demonstrate that substantial mantle heterogeneity is concealed in the lower oceanic crust and that melts derived from distinct mantle components can be delivered to the lower crust on a centimetre scale. These findings provide a starting point for re-evaluation of models of plate recycling, mantle convection and melt transport in the mantle and the crust.
Nature Communications, doi.org/10.1038/ s41467-019-11072-5 10p. Pdf
Europe, Italy
subduction
Abstract: Recycling of Earth’s crust through subduction and delamination contributes to mantle heterogeneity. Melt inclusions in early crystallised magmatic minerals record greater geochemical variability than host lavas and more fully reflect the heterogeneity of magma sources. To date, use of multiple isotope systems on small (300 ?m) melt inclusions was hampered by analytical limitations. Here we report the first coupled Sr-Nd-Pb isotope data on individual melt inclusions from potassium-rich lavas from neighbouring Quaternary volcanoes in central Italy and infer the presence of a previously unidentified ancient lower crustal component in the mantle. We suggest derivation from Variscan or older basement included in the upper mantle by either delamination, sediment recycling, subduction erosion and/or slab detachment processes during Cenozoic subduction and collision of the western Mediterranean. The capability to determine isotope ratios in individual melt inclusions permits the detection of distinctive mantle contaminants and can provide insights into how geodynamic processes affect subduction recycling.
Abstract: Partial melting of Earth’s mantle generates oceanic crust and leaves behind a chemically depleted residual mantle. The time-integrated composition of this chemically depleted mantle is generally inferred from basalts produced at mid-ocean ridges. However, isotopic differences between oceanic mantle rocks and mid-ocean ridge basalts suggest that mantle and basalt composition could differ. Here we measure neodymium isotope ratios in olivine-hosted melt inclusions from lavas of the Azores mantle plume. We find neodymium isotope ratios that include the highest values measured in basalts, and suggest that melts from ultra-depleted mantle contribute to the isotopic diversity of the erupted lavas. Ultra-depleted melts have exceedingly low preservation potential during magma extraction and evolution due to progressive mixing with melts that are enriched in incompatible elements. A notable contribution of ultra-depleted melts to the Azores mantle plume therefore implies that variably depleted mantle is the volumetrically dominant component of the Azores plume. We argue that variably depleted mantle, sometimes ranging to ultra-depleted compositions, may be a ubiquitous part of most ocean island and mid-ocean ridge basalt sources. If so, Earth’s mantle may be more depleted than previously thought, which has important implications for the rate of mass exchange between crust and mantle, plume dynamics and compositional stratification of Earth’s mantle.Depleted mantle is a volumetrically dominant component of the Azores plume and possibly of oceanic basalt sources more generally, according to neodymium isotope compositions of olivine-hosted melt inclusions from lavas of the Azores mantle plume.
Abstract: Precise analysis of 20xPb/204Pb ratios is challenging when the amount of Pb is limited by sample volume or elemental concentration. The current precision impedes meaningful analyses of analytes with sub-nanogram Pb contents, such as individual melt inclusions with typical diameters (<100 µm). Decreasing this lower limit whilst maintaining precision and accuracy is crucial for studies aiming to understand the composition and heterogeneity of melt source regions, and the effects of magma transport from the Earth’s interior. The preferred method for precise analysis of sub-nanogram Pb samples combines miniaturised ion-exchange separation, a Pb double spike, and thermal ionisation mass spectrometry (TIMS) with 10^13 ? amplifier technology. This approach allows for interference-free, instrumental mass fractionation-corrected isotope measurements, and therefore provides precision superior to in situ measurements. As a result, reliable analyses can be conducted on samples which contain only a few hundred picograms of Pb. The principal obstacle at the lower limit is the analytical blank, which usually adds a few pg Pb—and thus up to a few percent—to the sample of interest. This contribution may differ for the 207Pb-204Pb-spiked and unspiked runs of one sample, which in turn convolutes the algebraic inversion of the spike. It is therefore imperative to evaluate the magnitude, isotope composition, and homogeneity of the blanks, and constrain how the uncertainty and potential variability within these parameters affect the inversion. Here, we describe the optimised analytical techniques, and discuss the present feasibility and limitations in obtaining precise Pb isotope compositions of rock reference materials and olivine-hosted melt inclusions with sub-nanogram Pb contents. In addition, we discuss the effect of different blank contributions on double-spike analyses using numerical simulations, and evaluate the potential of accurate blank corrections. We find that the optimised technique allows accurate Pb analyses to be conducted on melt inclusions with >200 pg Pb, which will ultimately help to better constrain mantle heterogeneity beneath mid-ocean ridges, oceanic islands, and volcanic arcs.
Geochimica et Cosmochimica Acta, Vol. 293, pp. 1-17. pdf
Africa, Botswana
deposit - Jwaneng
Abstract: Constraining the formation age of individual diamonds from incorporated mineral inclusions and assessing the host diamonds’ geochemical characteristics allows determination of the complex history of diamond growth in the sub-continental lithospheric mantle (SCLM). It also provides the rare opportunity to study the evolution of the deep cycling of volatiles over time. To achieve these aims, Sm-Nd isotope systematics are presented for 36 eclogitic garnet and clinopyroxene inclusions from 16 diamonds from the Jwaneng mine, Botswana. The inclusions and host diamonds comprise at least two compositional suites that record different ‘mechanisms’ of diamond formation and define two isochrons, one Paleoproterozoic (1.8?Ga) and one Neoproterozoic (0.85?Ga). There are indications of at least three additional diamond-forming events whose ages currently cannot be well constrained. The Paleoproterozoic diamond suite formed by large-scale (>100?s km), volatile-rich metasomatism related to formation and re-working of the Proto-Kalahari Craton. In contrast, the heterogeneous composition of the Neoproterozoic diamond suite indicates diamond formation on a small-scale, through local (<10?km) equilibration of compositionally variable diamond-forming fluids in different eclogitic substrates during the progressive breakup of the Rodinia supercontinent. The results demonstrate that regional events appear to reflect the input of volatiles (i.e., carbon-bearing) derived from the asthenospheric mantle, whereas local diamond-forming events mainly promote the redistribution of volatiles within the SCLM. The occurrence of isotopically light carbon analysed in distinct growth zones from samples of this study (?13C??21.1‰) provides further indication of a recycled origin for surface-derived carbon in some diamonds from Jwaneng. Determining Earth’s long-term deep carbon cycle using diamonds, however, requires an understanding of the nature and scale of specific diamond-forming events.
Abstract: Thirty-nine garnet harzburgites from Kimberley in the Kaapvaal Craton (South Africa) were studied to constrain the origin, age and evolution of sub-cratonic lithospheric mantle (SCLM). In order to avoid chemical overprinting by recent metasomatism, only garnet harzburgites that appeared clinopyroxene-free to the naked eye were sampled. The majority of garnets were, however, in equilibrium with clinopyroxene (24 of 39). Whole rock and mineral major-trace element geochemistry and garnet Sr-Nd-Hf isotope data are presented. Equilibration pressures range from 3.8-6.1?GPa, indicating the harzburgites were derived from a large portion of the SCLM (~115-185?km). High olivine Mg# (~93.4, n?=?39) and low whole rock heavy rare earth elements (HREE) contents are consistent with large degrees of partial melting (>45%) and garnet exhaustion leaving a dunitic residue with olivine ?90%, orthopyroxene ?10% and HREE <0.01 times chondrite. Mineral modes, whole rock Al2O3 (0.5-3.2?wt%) and SiO2 (43.1-49.1?wt%), however, indicate heterogeneous re-introduction of garnet (?13%) and orthopyroxene (?50%). Harzburgites with high garnet and relatively low orthopyroxene modes (mostly ~7-13% and?~?9-30%; n?=?6) are characterised by mildly sinusoidal garnet REE patterns (Tbsingle bondDy minimum and high HREE) and Archaean depleted Hf TDM ages (2.7-3.3?Ga; ?Hfe: +190 to +709). In contrast, harzburgites with high orthopyroxene and relatively low garnet and modes (~1.5-7.5% and?~?25-50%; n?=?19) are characterised by highly sinuous REE patterns (Hosingle bondYb minimum and low HREE) and Proterozoic enriched Hf TDM ages (0.7-1.6?Ga; ?Hfe: ?16 to +6). It is inferred that Archaean G10 garnet re-introduction caused a significant increase in HREE, making melt depletion models based on HREE inaccurate. Orthopyroxene addition, a few hundred million years later, most likely at ~2.7?Ga and associated with Ventersdorp magmatic activity, caused partial consumption of garnet and olivine, and changed garnet compositions leading to: 1) Cr/Al ratio increase; 2) HREE decrease; 3) more sinusoidal REE patterns; and 4) un-radiogenic 176Hf/177Hf. Garnets define a Lusingle bondHf isochron age of 2702?±?64?Ma (?Hfi?=?+44, n?=?31), which is interpreted as a consequence of partial isotopic equilibrium within the SCLM and mixing of the garnet- and orthopyroxene-rich metasomatic components. The low LILE contents and absence of Nbsingle bondTa anomalies are consistent with modal metasomatism caused by intra-plate magmatism. In addition, the REE signatures of metasomatic agents in equilibrium with the garnets suggest that carbonatitic melts and SiO2-rich hydrous melts were responsible for re-introduction of garnet and orthopyroxene, respectively. Srsingle bondNd isotope systematics were disrupted associated with kimberlite magmatism (Nd isochron: 217?±?58?Ma, ?Ndi?=?+4; n?=?34), consistent with recent G10 garnet transformation into G9 garnets (Ca?+?Fe-enriched). This event may have caused garnet addition (up to 1%), suggesting that garnet was formed or destroyed in at least 4 different events: i) initial extensive polybaric melting, ii) asthenospheric melts re-introducing the bulk of the garnet, iii) orthopyroxene addition and garnet loss, all in the Archaean, and iv) minor garnet addition possibly related to recent kimberlite magmatism prior to eruption.
The Planetary Subcrustal Deep Fault System in North America: a New Concept of a Structural Control of Alkaline Magmatism,cryptoexplosion Structures and Related Ore Deposits.
Proceedings SECOND International CONFERENCE ON BASEMENT TECTONICS, No. 2, PP. 472- 483.
Journal of Mining Science, Vol. 53, 1, pp. 126-132.
Russia
deposit - Mir
Abstract: The structural and chemical surface transformation of basic kimberlite-forming minerals (calcite, olivine, serpentine) under the contact with natural and waste mineralized water and products of electrochemical treatment of the water are studied using X-ray photoelectronic spectroscopy, scanning electron microscopy and X-ray spectral micro-analysis, and atomic force microscopy. It is found that contact with kimberlite extract and recycling water induces chemical modification of calcite surface, which consists in adsorption of hydrocarbon impurities, and chlorine- and silica-bearing compounds, majority of which are removed during interaction with the product of electrochemical treatment of recycling water. The change in the structural and chemical surface properties of rock-forming silicates, aside from adsorption-desorption of organic compound, is also connected with the distortion of nano-size layer structure after leaching of Mg, Fe and Si, and with the carbonatization of the surface.
Abstract: The silico?carbonatite dykes of the Huanglongpu area, Lesser Qinling, China, are unusual in that they are quartz-bearing, Mo-mineralised and enriched in the heavy rare earth elements (HREE) relative to typical carbonatites. The textures of REE minerals indicate crystallisation of monazite-(Ce), bastnäsite-(Ce), parisite-(Ce) and aeschynite-(Ce) as magmatic phases. Burbankite was also potentially an early crystallising phase. Monazite-(Ce) was subsequently altered to produce a second generation of apatite, which was in turn replaced and overgrown by britholite-(Ce), accompanied by the formation of allanite-(Ce). Bastnäsite and parisite where replaced by synchysite-(Ce) and röntgenite-(Ce). Aeschynite-(Ce) was altered to uranopyrochlore and then pyrochlore with uraninite inclusions. The mineralogical evolution reflects the evolution from magmatic carbonatite, to more silica-rich conditions during early hydrothermal processes, to fully hydrothermal conditions accompanied by the formation of sulphate minerals. Each alteration stage resulted in the preferential leaching of the LREE and enrichment in the HREE. Mass balance considerations indicate hydrothermal fluids must have contributed HREE to the mineralisation. The evolution of the fluorcarbonate mineral assemblage requires an increase in aCa2+ and aCO32? in the metasomatic fluid (where a is activity), and breakdown of HREE-enriched calcite may have been the HREE source. Leaching in the presence of strong, LREE-selective ligands (Cl?) may account for the depletion in late stage minerals in the LREE, but cannot account for subsequent preferential HREE addition. Fluid inclusion data indicate the presence of sulphate-rich brines during alteration, and hence sulphate complexation may have been important for preferential HREE transport. Alongside HREE-enriched magmatic sources, and enrichment during magmatic processes, late stage alteration with non-LREE-selective ligands may be critical in forming HREE-enriched carbonatites.
Abstract: Using numerical thermo?mechanical experiments we analyse the role of an active mantle plume and pre?existing lithospheric thickness differences in the structural development of the central and southern East African Rift system. The plume?lithosphere interaction model setup captures the essential features of the studied area: two cratonic bodies embedded into surrounding lithosphere of normal thickness. The results of the numerical experiments suggest that localization of rift branches in the crust is mainly defined by the initial position of the mantle plume relative to the cratons. We demonstrate that development of the Eastern branch, the Western branch and the Malawi rift can be the result of non?uniform splitting of the Kenyan plume, which has been rising underneath the southern part of the Tanzanian craton. Major features associated with Cenozoic rifting can thus be reproduced in a relatively simple model of the interaction between a single mantle plume and pre?stressed continental lithosphere with double cratonic roots.
Geophysical Research Letters, Vol. 46, 7, pp. 3663-3675.
Mantle
subduction
Abstract: Separation of microcontinental blocks from their parent continent is usually attributed to abrupt relocation of concentrated extension from the mid?oceanic ridge to the adjacent continental margin. In the context of extensional passive margin evolution, previous extensive numerical and analog studies have revealed that hot upwelling mantle flow plays a key role in the mechanical weakening of the passive margin lithosphere needed to initiate a ridge jump. This, in turn, results in continental breakup and subsequent microcontinent isolation. However, the consequences of mantle plume impingement on the base of a moving lithospheric plate that is already involved into subduction are still unexplored quantitatively. Here we present the results of 3?D thermo?mechanical models showing that even in the context of induced plate motion (contractional boundary conditions), which are necessary to sustain continuous convergence, thermal and buoyancy effects of the mantle plume emplaced at the bottom of the continental part of the subducting plate are sufficient to initiate continental breakup and the subsequent opening of a new oceanic basin that separates the microcontinental block from the main body of the continent. With these models, we show that it is physically possible to form microcontinents in a convergent setting without the cessation of subduction.
Contributions to Mineralogy and Petrology, Vol. 171, 2p.
Mantle
Harzburgite
Abstract: Using the Hill et al. (Contrib Mineral Petrol 169:13, 2015. doi:10.1007/s00410-014-1102-7) modeling technique, we have tested the idea of Ivanic et al. (Contrib Mineral Petrol 164:505-520, 2012) that decompression and metamorphic re-equilibration of garnet with spinel causes garnet zoning perpendicular to the Cr-Ca harzburgitic trend in garnet composition. The modeling confirms that garnet zoning across the harzburgitic trend cannot form without spinel buffering. The harzburgitic trend is very rare because it results from extreme compositional heterogeneity of the mantle at the same depth. In contrast, the common lherzolitic trend requires less diversity in the bulk composition of the mantle, as it can be established with only a few samples of metamorphically re-equilibrated mantle peridotite deriving from a variety of depths.
The Archean- Paleoproterozoic evolution of the western margin of the Slave Craton and its influence on on-craton diamonds. Second talk same day: The role of subduction in the distribution of eclogite below the Slave Craton.
Vancouver Kimberlite Cluster, Oct. 7, 1p. Abstract
Peridotite xenoliths of the Chidliak kimberlite province (NE Canada): The North Atlantic cratonic mantle with recent thermal and Ti-Na metasomatic disturbance.
Hydration of the lithospheric mantle in the northern Slave craton ( Canada): constraints from combined FTIR and ESRD measurements on peridotite xenoliths.
Abstract: The mantle beneath the Cullinan kimberlite (formerly known as "Premier") is a unique occurrence of diamondiferous cratonic mantle where diamonds were generated contemporaneously and shortly following a mantle upwelling that led to the formation of a Large Igneous Province that produced the world's largest igneous intrusion - the 2056?Ma Bushveld Igneous Complex (BIC). We studied 332 diamond inclusions from 202 Cullinan diamonds to investigate mantle thermal effects imposed by the formation of the BIC. The overwhelming majority of diamonds come from three parageneses: (1) lithospheric eclogitic (69%), (2) lithospheric peridotitic (21%), and (3) sublithospheric mafic (9%). The lithospheric eclogitic paragenesis is represented by clinopyroxene, garnet, coesite and kyanite. Main minerals of the lithospheric peridotitic paragenesis are forsterite, enstatite, Cr-pyrope, Cr-augite and spinel; the sublithospheric mafic association includes majorite, CaSiO3 phases and omphacite. Diamond formation conditions were calculated using an Al-in-olivine thermometer, a garnet-clinopyroxene thermometer, as well as majorite and Raman barometers. The Cullinan diamonds may be unique on the global stage in recording a cold geotherm of 40?mW/m2 in cratonic lithosphere that was in contact with underlying convecting mantle at temperatures of 1450-1550?°C. The studied Cullinan diamonds contain a high proportion of inclusions equilibrated at temperatures exceeding the ambient 1327?°C adiabat, i.e. 54% of eclogitic diamonds and 41% of peridotitic diamonds. By contrast, ? 1% of peridotitic diamond inclusions globally yield equally high temperatures. We propose that the Cullinan diamond inclusions recorded transient, slow-dissipating thermal perturbations associated with the plume-related formation of the ~2?Ga Bushveld igneous province. The presence of inclusions in diamond from the mantle transition zone at 300-650?km supports this view. Cullinan xenoliths indicative of the thermal state of the cratonic lithosphere at ~1.2?Ga are equilibrated at the relatively low temperatures, not exceeding adiabatic. The ability of diamonds to record super-adiabatic temperatures may relate to their entrainment from the deeper, hotter parts of the upper mantle un-sampled by the kimberlite in the form of xenoliths or their equilibration in a younger lithosphere after a decay of the thermal disturbance.
Nestola, F., Korolev, N., Kopylova, M., Rotiroti, N., Pearson, D.G., Pamato, M.G., Alvaro, M., Peruzzo, L., Gurney, J.J., Moore, A.E., Davidson, J.
CaSiO3 perovskite in diamond indicates the recycling of oceanic crust into the lower mantle.
Nature, Vol. 555, March 8, pp. 237-241.
Mantle
deposit - Cullinan
Abstract: Laboratory experiments and seismology data have created a clear theoretical picture of the most abundant minerals that comprise the deeper parts of the Earth’s mantle. Discoveries of some of these minerals in ‘super-deep’ diamonds—formed between two hundred and about one thousand kilometres into the lower mantle—have confirmed part of this picture1,2,3,4,5. A notable exception is the high-pressure perovskite-structured polymorph of calcium silicate (CaSiO3). This mineral—expected to be the fourth most abundant in the Earth—has not previously been found in nature. Being the dominant host for calcium and, owing to its accommodating crystal structure, the major sink for heat-producing elements (potassium, uranium and thorium) in the transition zone and lower mantle, it is critical to establish its presence. Here we report the discovery of the perovskite-structured polymorph of CaSiO3 in a diamond from South African Cullinan kimberlite. The mineral is intergrown with about six per cent calcium titanate (CaTiO3). The titanium-rich composition of this inclusion indicates a bulk composition consistent with derivation from basaltic oceanic crust subducted to pressures equivalent to those present at the depths of the uppermost lower mantle. The relatively ‘heavy’ carbon isotopic composition of the surrounding diamond, together with the pristine high-pressure CaSiO3 structure, provides evidence for the recycling of oceanic crust and surficial carbon to lower-mantle depths.https://www.nature.com/articles/nature25972
Mineralogy and Petrology, doi.org/10.1007/s710-018-0601-z 15p.
Africa, South Africa
deposit - Cullinan
Abstract: We studied a suite of Cullinan diamonds (<0.3 ct) with mineral inclusions, which comprised 266 Type I and 75 blank Type II (<20 ppm N) diamonds, as classified by infrared spectroscopy. More than 90% (n?=?68) of Type II diamonds do not luminesce. In contrast, 51.9% (n?=?177) of Type I diamonds luminesce, with blue colors of different intensity. Carbon isotopic compositions of Type I and II diamonds are similar, with ?13CVPDB ranging from ?2.1 to ?7.7‰for Type I diamonds (n?=?25), and from ?1.3 to ?7.8- for Type II diamonds (n?=?20). The Type II diamonds are sourced from three parageneses, lithospheric lherzolitic (45%), lithospheric eclogitic (33%), and sublithospheric mafic (22%). The lherzolitic suite contains Cr-pyrope, forsterite, enstatite, clinopyroxene and Cr-spinel formed at 1090-1530 °C and P?=?4.6-7.0 GPa. Lithospheric eclogitic diamonds containing garnet, omphacite, kyanite and coesite comprise 33% of Type II diamonds. The sublithospheric mafic paragenesis is mainly represented by Cr-free majorite, various CaSiO3 phases and omphacite equilibrated at 11.6-26 GPa, in the transition zone and the lower mantle. The lherzolitic paragenesis predominates in Type II diamonds, whereas 79% Type I diamonds are sourced from eclogites. The higher incidence of sublithospheric inclusions was found in Type II diamonds, 22% against 6% in Type I diamonds. The similarity of the mineral parageneses and C isotopic compositions in the small Cullinan Type II and Type I diamonds indicate the absence of distinct mantle processes and carbon sources for formation of studied Type II diamonds. The parent rocks and the carbon sources generally vary for Type II diamonds within a kimberlite and between kimberlites.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0633-4 13p.
Canada, Quebec
deposit - Renard
Abstract: Renard 65, a diamondiferous pipe in the Neoproterozoic Renard kimberlite cluster (Québec, Canada), is a steeply-dipping and downward-tapering diatreme comprised of three pipe-filling units: kimb65a, kimb65b, and kimb65d. The pipe is surrounded by a marginal and variably-brecciated country rock aureole and is crosscut by numerous hypabyssal dykes: kimb65c. Extensive petrographic and mineralogical characterization of over 700 m of drill core from four separate drill holes, suggests that Renard 65 is a Group I kimberlite, mineralogically classified as phlogopite kimberlite and serpentine-phlogopite kimberlite. Kimb65a is a massive volcaniclastic kimberlite dominated by lithic clasts, magmaclasts, and discrete olivine macrocrysts, hosted within a fine-grained diopside and serpentine-rich matrix. Kimb65b is massive, macrocrystic, coherent kimberlite with a groundmass assemblage of phlogopite, spinel, perovskite, apatite, calcite, serpentine and rare monticellite. Kimb65c is a massive, macrocrystic, hypabyssal kimberlite with a groundmass assemblage of phlogopite, serpentine, calcite, perovskite, spinel, and apatite. Kimb65d is massive volcaniclastic kimberlite with localized textures that are intermediate between volcaniclastic and coherent, with tightly packed magmaclasts separated by a diopside- and serpentine-rich matrix. Lithic clasts of granite-gneiss in kimb65a are weakly reacted, with partial melting of feldspars and crystallization of richterite and actinolite. Lithic clasts in kimb65b and kimb65d are entirely recrystallized to calcite + serpentine/chlorite + pectolite and display inner coronas of diopside-aegirine and an outer corona of phlogopite. Compositions are reported for all minerals in the groundmass of coherent kimberlites, magmaclasts, interclast matrices, and reacted lithic clasts. The Renard 65 rocks are texturally classified as Kimberley-type pyroclastic kimberlites and display transitional textures. The kimberlite units are interpreted to have formed in three melt batches based on their distinct spinel chemistry: kimb65a, kimb65b and kimb65d. We note a strong correlation between the modal abundances of lithic clasts and the textures of the kimberlites, where increasing modal abundances of granite/gneiss are observed in kimberlites with increasingly fragmental textures.
Abstract: Carbonate-rich intrusions in contact with felsic rocks theoretically should show the effects of interaction between the two rock types, due to their contrasting compositions. In reality, though, such interaction is rarely reported at kimberlite contacts. We present the first documented case of lithological and mineralogical zonation at the margin of a kimberlite, the Snap Lake dyke, in contact with the wall-rock granitoid. Our detailed petrographic, mineralogical and geochemical study shows that the fresh hypabyssal kimberlite consists of olivine macrocrysts and microcrysts, and phlogopite macrocrysts set in a groundmass of serpentinized monticellite, phlogopite, spinel, perovskite and apatite, with interstitial lizardite and calcite. This typical Group I kimberlite mineralogy does not match the bulk-rock composition, which resembles a Group II micaceous kimberlite. The mismatch between the chemical and mineralogical properties is ascribed to contamination by granitoid xenoliths and metasomatic reactions with the felsic country rocks, the Snap Lake kimberlite has extremely low bulk-Ca compared to other documented Group I kimberlites. Reaction with deuteric H2O and CO2 has led to Ca removal, serpentinization of olivine, replacement of calcite by dolomite, alteration of perovskite and decomposition of apatite. Adjacent to the contact with the host granitoid and in haloes around granitoid clasts, poikilitic phlogopite and lizardite are replaced by subsolidus phlogopite and a multiphase phyllosilicate composed of phlogopite+?lizardite+?chlorite+?talc. A modified isocon analysis accounts for felsic xenolith assimilation and isolates metasomatic changes. Enrichment of altered kimberlites in Si owes solely to xenolith incorporation. The metasomatic ingress of granitoid-derived Al for a limited distance inside the dyke was counteracted by a flux of Mg and Fe to the granitoid. Metasomatic changes in K and Ca tend to be positive in all lithologies of kimberlite and in the granitoids implying distal transport. The combination of xenolith digestion with metasomatic element transport is expected in hybrid zones where kimberlite magmas interact with felsic wall-rocks.
Geochemical Perspectives Letters, Vol. 9, pp. 6-10. 10.7185/geochemlet.1830
Mantle
peridotites
Abstract: The origin of the peridotites that form cratonic mantle roots is a central issue in understanding the history and survival of Earth’s oldest continents. A long-standing hypothesis holds that the unusual bulk compositions of some cratonic peridotites stem from their origin as subducted oceanic serpentinite, dehydrated during subduction to form rigid buoyant keels (Schulze, 1986; Canil and Lee, 2009). We present oxygen isotope data from 93 mantle peridotites from five different Archean cratons to evaluate their possible origin as serpentinites. Cratonic mantle peridotite shows remarkably uniform ?18O values, identical to modern MORB-source mantle, that do not vary with bulk rock Si-enrichment or Ca-depletion. These data clearly conflict with any model for cratonic lithosphere that invokes serpentinite as a protolith for cratonic peridotite, and place additional constraints on cratonic mantle origins. We posit that the uniform ?18O was produced by sub-arc and/or MOR depletion processes and that the Si-enriched nature of some samples is unlikely to be related to slab melt infiltration. Instead, we suggest a peridotitic source of Si-enrichment, derived from ascending mantle melts, or a water-fluxed depleted mantle. These variably Si-enriched, cratonic mantle protoliths were then collisionally compressed into the thick cratonic roots that have protected Earth’s oldest continental crust for over 2.5 Gyr.
Fulop, A., Kopylova, M., Kurszlaukis, S., Hilchie, L., Ellemers, P.
A reply to the comment by Germon et al. on the Petrography of the Snap Lake kimberlite dyke ( Northwest Territories, Canada) and its interaction with country rock granitoids.
Abstract: Megacrysts are mineral grains of garnet, clinopyroxene, orthopyroxene, ilmenite, olivine, phlogopite and zircon larger than 10 mm frequently observed in kimberlite occurrences across the world, with reported sizes commonly exceeding 10 cm. Despite their common occurrence and decades of research into their origin, megacryst petrogenesis is still a debated topic amongst petrologists. A strictly phenocrystal origin is doubted, with recent research suggesting a multi-stage model involving isobaric formation over a wide temperature range, followed by metasomatism of a protokimberlite fluid that replaces mantle minerals. Our project aims to contribute to ongoing research by modeling the metasomatism of the ambient peridotitic mantle affected by the fluid using major and trace element data obtained from megacrysts from the Jurassic Muskox kimberlite pipe of the Slave province of Canada. We report major element compositions of 24 megacryst samples of garnet, olivine, clinopyroxene and ilmenite and employ DEW (Deep Earth Water) modelling to establish the composition of the potential metasomatizing agent and mineral trends that result from the mantle metasomatism. This project has important implications for not only constraining the composition of the source fluids, but also understanding the reactions in the cratonic mantle leading to the kimberlite melt formation.
Abstract: We studied the petrography, mineralogy, thermobarometry and whole rock chemistry of 120 peridotite and pyroxenite xenoliths collected from the 156 - 138 Ma Chidliak kimberlites CH-1, -6, -7 and -44. The xenoliths have higher CaO contents relative to Al2O3, and high Al for a given Mg/Si ratio compared to other cratonic peridotites. We assign the complex Ca-Al systematics of the Chidliak peridotites to repeated episodes of Ca-rich, Si-poor metasomatism, which introduced clinopyroxene and garnet, and later replaced orthopyroxene and clinopyroxene with secondary clinopyroxene and monticellite. This carbonatitic metasomatism, manifest in formation of wehrlites, acted upon the entire sampled mantle depth on a regional scale, including the proximal blocks of the North Atlantic Craton and the Chidliak mantle, where clinopyroxene and garnet modes are uniformly and heterogeneously high in the ~ 110 km deep mantle segment. Another, more recent type of mantle metasomatism, is expressed as elevated Ti in clinopyroxene and elevated Na and Ti in garnet, typical of sheared peridotites from CH-1, -7, and -44, but absent from CH-6 xenolith suite. The Ti-Na imprint is most intense in xenoliths derived from depths equivalent to 5.5 to 6.5 GPa, where it is associated with higher strain, the presence of sheared peridotites and higher temperatures varying isobarically by up to 200 °C. The horizontal scale of the thermal-metasomatic imprint is more ambiguous and could be as regional as 10's of kilometers or as local as < 1 km. The latter is constrained by the varied abundance of Ti-enriched garnets within a single kimberlite. The time-scale of this metasomatism relates to a conductive length-scale and could be as short as 100's ka, shortly predating the kimberlite formation. The Ti-Na, megacryst-like metasomatism may have resulted from a highly localized influx of hot hydrous proto-kimberlite fluids that weakened the mantle and triggered the formation of sheared peridotites.
Abstract: Kimberlites often entrain crustal felsic xenoliths, which show alteration and metamorphism as a result of interaction with the host kimberlite. We studied granite and gneiss xenoliths in the Renard 65 kimberlite pipe (Northern Québec, Canada). The study comprised a detailed petrographic examination of 45 thin sections, a scanning electron microscopy and an X-ray powder diffractometry of a sample sub-set. Two major units of the Renard 65 pipe (Unit A and Unit B/D) distinguished by abundance of crustal xenoliths along with the degree of their alteration, were investigated. Unit A is a volcaniclastic kimberlite with 40-90 % xenoliths, whereas Unit B/D is a hypabyssal kimberlite with textures transitional to pyroclastic, containing 15-40 % more intensely altered xenoliths. Both units carry xenoliths of coarse-grained leucogranite (K-feldspar, plagioclase, quartz, biotite with accessory garnet, apatite, and zircon) and medium-grained gneiss (plagioclase, quartz, biotite, orthopyroxene with accessory garnet, apatite and zircon). The Unit A xenoliths are partially replaced by chlorite, sericite, epidote, serpentine, richterite, actinolite and clinochlore vermiculite. In Unit B/D four distinct metamorphic and metasomatic mineral assemblages almost completely replace xenoliths. The assemblages include aegirine, pectolite, garnet, wollastonite, xonotlite, prehnite, calcite, K-feldspar and richterite in various proportions. Secondary K-feldspar and calcite may indicate the granite protolith, whereas wollastonite may be the signature of the gneiss protolith. The presence of secondary garnet and wollastonite, the hallmark skarn minerals, suggests the analogy between the classical skarn geological processes at the contact between felsic rocks and the host hot carbonate-rich melts. The observed mineralogy of the Renard 65 felsic xenoliths will be compared with the theoretically predicted mineralogy modelled using Theriak-Domino or Perplex software for the known bulk hybrid kimberlite compositions. The comparison will enable constraints on temperatures, volatile contents and thermal history of the kimberlite melt during emplacement.
Abstract: Cratons are the ancient landmasses that remain stable for billions of years on Earth but also have experienced episodic events of modification and rejuvenation throughout their history [1]. These alteration processes have modified the cratonic lithospheric mantle roots to different extents, e.g., ubiquitous cryptic/modal metasomatism, partial to entire loss of the mantle roots, to rifting apart of the craton. It remains unclear to what extent a cratonic mantle root can withstand modification and retain its integrity. We attempt to discuss this issue from the perspective of the Slave craton that has experienced the multiple impacts of major circum-cratonic Paleoproterozoic (1.93-1.84 Ga) orogenies and the intrusion of several 2.23-1.67 Proterozoic diabase dyke swarms. We use kimberlite-borne peridotite xenoliths to construct a N-S transect across the craton with an aim of probing the effects of these post-Archean events on the composition, age and depth of the lithospheric root. Chemically, all of these rocks are of typical cratonic refractory composition. P-T calculations and paleogeotherms show that they were derived from thick lithospheric mantle roots (>180 km), consistent with their diamondiferous nature. However, these peridotites exhibit variable N-S variation of modes in their Re-depletion Os model ages (TRD). Neoarchean TRD ages dominate in the Central and Southern Slave mantle. Progressing North there is a decreasing proportion of Archean TRD ages through Jericho to Artemisa in the Northern Slave craton. About 70% of the peridotites at Artemisia give TRD ages within error of the ~1.27 Ga Mackenzie LIP event, with the remaining (~ 30%) close to the Paleoproterozoic orogenic events. Combined with new data from regions to the N and NW of the Slave craton [2], the observed age spectrum in the far North of the craton indicates the likelihood of major new generation of lithospheric roots in both the Paleoproterozoic and Mesoproterozoic. Despite its complex history, the Northern Slave craton retains a ‘cratonic-like’ lithospheric root that allowed diamond mineralization.
Contributions to Mineralogy and Petrology, Vol. 175, 8, 25p. Pdf
Canada, Baffin Island
deposit - Chidliak
Abstract: The 156-138 Ma Chidliak kimberlites on the Eastern Hall peninsula (EHP) of Baffin Island entrained mantle xenoliths interpreted to have been a part of the Archean North Atlantic Craton (NAC) lithospheric mantle. We studied 19 Chidliak eclogite xenoliths that comprise 10 bimineralic, 5 rutile-bearing, 3 orthopyroxene-bearing and 1 kyanite-bearing eclogites. We report major and trace element compositions of the minerals, calculated bulk compositions, pressures and temperatures of the rock formation and model melt extraction from viable protoliths. The eclogite samples are classified into three groups of HREE-enriched, LREE-depleted and metasomatized based on their reconstructed whole-rock REE patterns. PT parameters of the eclogites were calculated by projecting garnet-clinopyroxene temperatures onto the local P-T arrays for 65 Chidliak peridotite xenoliths. All Chidliak eclogites are equilibrated in the diamond P-T field and cluster in two groups, low-temperature (n?=?5, 840-990 °C at 4.1-5.0 GPa) and high-temperature (n?=?11, T?>?1320 °C at P?>?7.0 GPa). The reconstructed Mg-rich major element bulk compositions and trace elements patterns are similar to Archean basalts from the North Atlantic and Superior cratons and the oceanic gabbros. The LREE-depleted Chidliak eclogites could be residues after 15-55% partial melting of Archean basalt at the eclogite facies of metamorphism that led to extraction of a tonalite-trondhjemite-granodiorite melt from the EHP. The HREE-depleted eclogites may have experienced a lower degree (<10%) of partial melting. Two eclogites may have formed after the gabbro protolith based on the presence of kyanite, high Sr content of garnet and positive Eu anomalies in garnet and bulk eclogite compositions. The metasomatism is reflected in higher Ce/Yb, Sr/Y, TiO2 or MgO of the eclogites. The average contents of MgO, FeO and CaO in NAC eclogites are statistically distinct from those in Slave craton eclogites with a probability of?>95%. The former are more magnesian, less ferrous and calcic, contain more magnesian and less calcic garnets, and lower proportions of group C eclogites. The contrast may relate to the stronger NAC metasomatism by silicate-carbonate melt observed in Chidliak peridotitic mantle, or to the different formation ages of the eclogites beneath the two cratons.
Journal of the Geological Society, doi.org/10.1144 /jgs2020-184 53p. Pdf
Canada, Northwest Territories
deposit - Muskox
Abstract: Low-Cr and high-Cr clinopyroxene, garnet, olivine, and ilmenite megacrysts from the Muskox kimberlite (Canada) have been analyzed for major and trace elements, as well as Sr, Nd, and Pb isotopes. Samples display compositional overlap with respective phases in websterite, while clinopyroxene isotope systematics reveal similarities with both websteritic and metasomatic clinopyroxene in peridotites from the same kimberlite, in addition to Muskox and Jericho kimberlite. All lithologies may represent the products of mixing between EM1 mantle, relic Proterozoic enriched mantle and HIMU carbonatitic fluid. Equilibrium melts calculated from clinopyroxene trace element data using experimental distribution coefficients for feasible proto-kimberlitic melts yield a range of possible metasomatic agents. Conclusion on the carbonate-bearing nature of the metasomatism was based on the presence of a HIMU isotopic signature and results obtained from thermodynamic modeling using the Deep Earth Water model. The latter shows that mineral compositions analogous to megacrysts cannot be produced by metasomatism of mantle peridotite by H2O-rich kimberlitic fluids, or fluids in equilibrium with either asthenospheric or eclogitic mantle. Isotope systematics argue against a strictly cognate relationship between megacrysts and their host kimberlite, instead suggesting megacrysts and websterites may represent products of regional metasomatism by carbonatitic HIMU fluids shortly predating kimberlite magmatism.
Contributions to Mineralogy and Petrology, Vol. 176, 10, 28p. Pdf
Canada, Quebec
deposit - Renard
Abstract: This study aims to constrain the nature of kimberlite-xenolith reactions and the fluid origin for Kimberley-type pyroclastic kimberlite (KPK). KPKs are characterized by an abundance of basement xenoliths (15-90%) and display distinct pipe morphology, textures, and mineralogy. To explain the KPK mineralogy deviating from the mineralogy of crystallized kimberlite melt, we study reactions between hypabyssal kimberlite transitional to KPK and felsic xenoliths. Here, we characterize the pectolite-diopside-phlogopite-serpentine-olivine common zonal patterns using petrography, bulk composition, thermodynamic modelling, and conserved element ratio analysis. To replicate the observed mineral assemblages, we extended the thermodynamic database to include pectolite, using calculated density functional theory methods. Our modelling reproduces the formation of the observed distinct mineralogy in reacted granitoid and gneiss. The assimilation of xenoliths is a process that starts from high temperatures (1200-600 °C) with the formation of clinopyroxene and wollastonite, continues at 600-200 °C with the growth of clinopyroxene, garnet, and phlogopite finishing at temperatures?300 °C when pectolite and prehnite join in. Critically, the majority of the new mineral growth occurs in the sub-solidus, at temperatures below 600 °C. The metasomatic origin of the xenolith mineralogy is best explained by gradients in the chemical potentials of Si, Al, Ca, and Mg across the xenolith-kimberlite contacts. The low-temperature mineralogy of the fluid-limited thermodynamic calculations, where H2O and CO2 are controlled by kimberlite concentrations, reproduces the observed mineralogy better than a fluid-saturated model with a meteoric fluid composition. Our findings imply the deuteric origin of the fluids in KPK pipes controlling the kimberlite mineralogy and texture.
Abstract: Petrologists all agree that the “carbonated mantle”, i. e. peridotite with accessory carbonate, is necessary to generate CO2-bearing melts. Carbonated peridotite is also a useful theoretical concept for geochemists seeking to explain trace element enrichment of the lithospheric mantle. Melting of peridotite with addition of carbonate has been the subject of hundreds of experimental studies. Yet mantle samples from below cratons do not contain carbonate. Our work tries to reconcile the theoretical view of the carbonated mantle with the empirical observations on cratonic mantle xenoliths. Peridotite xenoliths from the Chidliak kimberlite province (SE Baffin Island, Canada) suggest that the natural carbonated mantle are peridotites with elevated modes of clinopyroxene, garnet and olivine, and with thin rims of calcic silicate minerals. Observations on Chidliak peridotites provide an excellent “reality check” for theoretical mobility models of the carbonate-rich melts in the mantle. The “carbonation freezing front” is often theoretically imagined as the solidus of mantle peridotites infiltrated by CO2-rich melts. Our observations suggest that melting is not necessary for immobilization of carbonatitic metasomatic agent. The latter is highly reactive, readily giving away Ca to silicate minerals and exsolving CO2. At Chidliak, clinopyroxene and monticellite rims produced by carbonation do not show signs of partial melting during their formation; moreover, thicker mantles of clinopyroxene in Chidliak peridotites are equilibrated at P-Ts below the CO2- saturated peridotite solidus. Petrography of Chidliak peridotites also constrains the melt flux in the carbonation freezing model. At melt fluxes >10%, the model predicts elevated fractions of the reacted melt in comparison with the reacting melt. This should lead to loss of Ca. Natural samples, on the contrary, demonstrate addition of Ca; this is observed from quantification of compositional fluxes at Chidliak and in temporal trends of mineral and bulk compositions of the cratonic mantle. This suggests that the carbonatitic fluxes are always below 10%, and the carbonate-rich melt always "freezes in" in peridotites. We further submit that CO2-rich magmas on cratons are byproducts of carbonate metasomatism, since deep decarbonation is a necessary prerequisite to generation of CO2-rich melts. Theoretically, carbonate-rich fluids should be able to traverse the peridotitic mantle in the reacted channels where the fluids overcome the limits of the mineralogical, thermal and redox instability in deep peridotites. This study suggests the channels can be made of garnet or clinopyroxene, as only these initial products of reactive decarbonation of the deep peridotitic mantle are observed to contain fluid microinclusions and modal macro- grains of carbonates. Future research will better recognize stealth signs of carbonatitic metasomatism under cratons and enable us to better document its extent and localization.
Abstract: A suite of peridotite xenoliths from the Chidliak kimberlite province provides an ideal opportunity to assess the age of the mantle lithosphere beneath the eastern Hall Peninsula Block (EHPB) in southern Baffin Island, Nunavut and to provide constraints on the lithospheric architecture of this region. The new dataset comprises highly siderophile element (HSE) abundances and Re-Os isotopic compositions for 32 peridotite xenoliths sampled from four Late Jurassic-Early Cretaceous kimberlite pipes (CH-1, -6, -7, and -44). These peridotites represent strongly depleted mantle residues, with bulk-rock and olivine chemistry denoting melt extraction extents of up to 40%. The vast majority of samples show PPGE (Pt and Pd) depletion relative to IPGE (Os, Ir, and Ru) ((Pt/Ir)N: 0.10-0.96, median = 0.57; (Pd/Ir)N: 0.03-0.79, median = 0.24), coupled with mostly unradiogenic Os isotopic compositions (187Os/188Os = 0.1084-0.1170). These peridotites display strong correlations between 187Os/188Os and melt depletion indicators (such as olivine Mg number and bulk-rock Al2O3, (Pd/Ir)N), suggesting that an ancient (~2.8 Ga) melt depletion event governed the formation of the Chidliak lithosphere. The prominent mode of TRDerupt model ages at ca. 2.8 Ga matches the main crust-building ages of the EHPB, demonstrating temporal crust-mantle coupled in the Meso-Neoarchean. These ancient melt-depletion ages are present throughout the depth of the ~ 200 km thick lithospheric mantle column beneath Chidliak. The Meso-Neoarchean formation age of the EHPB mantle broadly coincides with the timing of stabilization of the lithospheric mantle beneath the Greenlandic portion of the North Atlantic Craton (NAC). This, along with the similarity in modal mineralogy, chemical composition and evolutionary history, indicates that the EHPB, southern Baffin Island was once -contiguous with the Greenlandic NAC. The mantle lithosphere beneath both the EHPB and the NAC show a similar metasomatic history, modified by multiple pulses of metasomatism. These multiple metasomatic events combined to weaken and thin the lithospheric mantle, culminating in the formation of the Labrador Sea and Davis Strait separating the EHPB from the Greenlandic NAC in the Paleocene.
Abstract: Assimilation of country rock xenoliths by the host kimberlite can result in the development of concentric reaction zones within the xenoliths and a reaction halo in the surrounding contaminated kimberlite. Petrographic and geochemical changes across the reaction zones in the xenoliths and the host kimberlite were studied using samples with different kimberlite textures and contrasting xenolith abundances from the Renard 65 kimberlite pipe. The pipe, infilled by Kimberley-type pyroclastic (KPK) and hypabyssal kimberlite (HK) and kimberlite with transitional textures, was emplaced into granitoid and gneisses of the Superior Craton. Using samples of zoned, medium-sized xenoliths of both types, mineralogical and geochemical data were collected across xenolith-to-kimberlite profiles and contrasted with those of fresh unreacted country rock and hypabyssal kimberlite. The original mineralogy of the unreacted xenoliths (potassium feldspar-plagioclase-quartz-biotite in granitoid and plagioclase-quartz-biotite-orthopyroxene in gneiss) is replaced by prehnite, pectolite, and diopside. In the kimberlite halo, olivine is completely serpentinized and diopside and late phlogopite crystallized in the groundmass. The xenoliths show the progressive degrees of reaction, textural modification, and mineral replacement in the sequence of kimberlite units KPK — transitional KPK — transitional HK. The higher degree of reaction observed in the HK-hosted xenoliths as compared to the KPK-hosted xenoliths in this study and elsewhere may partly relate to higher temperatures in xenoliths included in an HK melt. The correlation between the degree of reaction and the kimberlite textures suggests that the reactions are specific to and occur within each emplaced batch of magma and cannot result from external post-emplacement processes that should obliterate the textural differences across the kimberlite units. Xenolith assimilation may have started in the melt, as suggested by the textures in the xenoliths and the surrounding halos and proceeded in the subsolidus. Elevated CaO at the kimberlite-xenolith contact appears to be an important factor in producing the concentric mineralogical zoning in assimilated xenoliths.
Abstract: Assimilation of country rock xenoliths by the host kimberlite can result in the development of concentric reaction zones within the xenoliths and a reaction halo in the surrounding contaminated kimberlite. Petrographic and geochemical changes across the reaction zones in the xenoliths and the host kimberlite were studied using samples with different kimberlite textures and contrasting xenolith abundances from the Renard 65 kimberlite pipe. The pipe, infilled by Kimberley-type pyroclastic (KPK) and hypabyssal kimberlite (HK) and kimberlite with transitional textures, was emplaced into granitoid and gneisses of the Superior Craton. Using samples of zoned, medium-sized xenoliths of both types, mineralogical and geochemical data were collected across xenolith-to-kimberlite profiles and contrasted with those of fresh unreacted country rock and hypabyssal kimberlite. The original mineralogy of the unreacted xenoliths (potassium feldspar-plagioclase-quartz-biotite in granitoid and plagioclase-quartz-biotite-orthopyroxene in gneiss) is replaced by prehnite, pectolite, and diopside. In the kimberlite halo, olivine is completely serpentinized and diopside and late phlogopite crystallized in the groundmass. The xenoliths show the progressive degrees of reaction, textural modification, and mineral replacement in the sequence of kimberlite units KPK — transitional KPK — transitional HK. The higher degree of reaction observed in the HK-hosted xenoliths as compared to the KPK-hosted xenoliths in this study and elsewhere may partly relate to higher temperatures in xenoliths included in an HK melt. The correlation between the degree of reaction and the kimberlite textures suggests that the reactions are specific to and occur within each emplaced batch of magma and cannot result from external post-emplacement processes that should obliterate the textural differences across the kimberlite units. Xenolith assimilation may have started in the melt, as suggested by the textures in the xenoliths and the surrounding halos and proceeded in the subsolidus. Elevated CaO at the kimberlite-xenolith contact appears to be an important factor in producing the concentric mineralogical zoning in assimilated xenoliths.
The exceptionally fresh Udachnaya-East kimberlite: evidence from brine and evaporite contamination.
Proceedings of the 10th. International Kimberlite Conference, Vol. 1, Special Issue of the Journal of the Geological Society of India,, Vol. 1, pp. 75-91.
Abstract: We reconstructed the spatial distribution of eclogites in the cratonic mantle based on thermobarometry for ~ 240 xenoliths in 4 kimberlite pipes from different parts of the Slave craton (Canada). The accuracy of depth estimates is ensured by the use of a recently calibrated thermometer, projection of temperatures onto well-constrained local peridotitic geotherms, petrological screening for unrealistic temperature estimates, and internal consistency of all data. The depth estimates are based on new data on mineral chemistry and petrography of 148 eclogite xenoliths from the Jericho and Muskox kimberlites of the northern Slave craton and previously reported analyses of 95 eclogites from Diavik and Ekati kimberlites (Central Slave). The majority of Northern Slave eclogites of the crustal, subduction origin occurs at 110-170 km, shallower than in the majority of the Central Slave crustal eclogites (120-210 km). The identical geochronological history of these eclogite populations and the absence of steep suture boundaries between the central and northern Slave craton suggest the lateral continuity of the mantle layer relatively rich in eclogites. We explain the distribution of eclogites by partial preservation of an imbricated and plastically dispersed oceanic slab formed by easterly dipping Proterozoic subduction. The depths of eclogite localization do not correlate with geophysically mapped discontinuities. The base of the depleted lithosphere of the Slave craton constrained by thermobarometry of peridotite xenoliths coincides with the base of the thickened lithospheric slab, which supports contribution of the recycled oceanic lithosphere to formation of the cratonic root. Its architecture may have been protected by circum-cratonic subduction and shielding of the shallow Archean lithosphere from the destructive asthenospheric metasomatism.
Journal of Volcanology and Geothermal Research, in press available 19p.
Russia
Deposit - Udachnaya East
Abstract: The Udachnaya East kimberlite is characterized by the presence of chlorides, sulfates and alkali carbonates. This highly atypical mineralogy underpinned a model for an anhydrous alkali-rich primary kimberlite melt, despite the absence of petrographic studies providing textural context to the exotic minerals. The present work documents the petrography of the Udachnaya East kimberlite in order to address this problem. The pipe comprises two varieties of Fort-a-la-Corne type pyroclastic kimberlite, olivine-rich and magmaclast-rich, and coherent kimberlite. These kimberlites entrain xenoliths of limestones, altered shales and siltstones, halite-dominated rocks, dolomites, and coarse calcite rocks. The distinct varieties of the Udachnaya East kimberlite carry different populations of crustal xenoliths, which partially control the mineralogy of the host kimberlite. In magmaclast-rich pyroclastic kimberlite, where halite is absent from the crustal xenoliths, it is not observed in the interclast matrix, or within the magmaclasts. Halite occurs in the interclast matrix of olivine-rich pyroclastic kimberlite, where halite xenoliths are common. Large, ~ 30 cm halite xenoliths are uniquely restricted to the coherent kimberlite and show a strong reaction with it. The halite xenoliths are sourced from depths of ? 1500 to ? 630 m, where carbonate beds host multiple karst cavities filled with halite and gypsum and occasional sedimentary evaporites. The style of secondary mineralization at Udachnaya depends on whether the kimberlite is coherent or pyroclastic. Shortite, pirssonite and other alkali carbonates replacing calcite and possibly serpentine are abundant only in porous pyroclastic kimberlites of both types and in their shale/siltstone xenoliths. The lower porosity of the coherent kimberlite prevented the interaction of kimberlite with Na brines. Serpentinization localized around halite xenoliths started at temperatures above 500 °C, as indicated by its association with high-temperature iowaite. The model of the “dry” Na and Cl-rich primary kimberlite melt is invalidated on the basis of 1) the restriction of exotic salt minerals to certain kimberlite types and xenoliths; and 2) the absence of halite-rich melt inclusions in olivine of coherent kimberlite.
Abstract: Alluvial diamonds from the Kasai River, Democratic Republic of the Congo (DRC) are sourced from Cretaceous kimberlites of the Lucapa graben in Angola. Analysis of 40 inclusion-bearing diamonds provides new insights into the characteristics and evolution of ancient lithospheric mantle of the Congo craton. Silicate inclusions permitted us to classify diamonds as peridotitic, containing Fo91-95 and En92-94, (23 diamonds, 70% of the suite), and eclogitic, containing Cr-poor pyrope and omphacite with 11-27% jadeite (6 diamonds, 18% of the suite). Fluid inclusion compositions of fibrous diamonds are moderately to highly silicic, matching compositions of diamond-forming fluids from other DRC diamonds. Regional homogeneity of Congo fibrous diamond fluid inclusion compositions suggests spatially extensive homogenization of Cretaceous diamond forming fluids within the Congo lithospheric mantle. In situ cathodoluminescence, secondary ion mass spectrometry and Fourier transform infrared spectroscopy reveal large heterogeneities in N, N aggregation into B-centers (NB), and ?13C, indicating that diamonds grew episodically from fluids of distinct sources. Peridotitic diamonds contain up to 2962 ppm N, show 0-88% NB, and have ?13C isotopic compositions from ? 12.5‰ to ? 1.9‰ with a mode near mantle-like values. Eclogitic diamonds contain 14-1432 ppm N, NB spanning 29%-68%, and wider and lighter ?13C isotopic compositions of ? 17.8‰ to ? 3.4‰. Fibrous diamonds on average contain more N (up to 2976 ppm) and are restricted in ?13C from ? 4.1‰ to ? 9.4‰. Clinopyroxene-garnet thermobarometry suggests diamond formation at 1350-1375 °C at 5.8 to 6.3 GPa, whereas N aggregation thermometry yields diamond residence temperatures between 1000 and 1280 °C, if the assumed mantle residence time is 0.9-3.3 Ga. Integrated geothermobaromtery indicates heat fluxes of 41-44 mW/m2 during diamond formation and a lithosphere-asthenosphere boundary (LAB) at 190-210 km. The hotter-than-average cratonic mantle may be attributable to contemporaneous rifting of the southern Atlantic, multiple post-Archean reactivations of the craton, and/or proximal Cretaceous plumes.
Canadian Journal of Earth Sciences, Vol. 53, 1, pp. 41-58.
Canada, Northwest Territories
Deposit - Muskox
Abstract: We present petrography, mineralogy, and thermobarometry for 53 mantle-derived xenoliths from the Muskox kimberlite pipe in the northern Slave craton. The xenolith suite includes 23% coarse peridotite, 9% porphyroclastic peridotite, 60% websterite, and 8% orthopyroxenite. Samples primarily comprise forsteritic olivine (Fo 89-94), enstatite (En 89-94), Cr-diopside, Cr-pyrope garnet, and chromite spinel. Coarse peridotites, porphyroclastic peridotites, and pyroxenites equilibrated at 650-1220 °C and 23-63 kbar (1 kbar = 100 MPa), 1200-1350 °C and 57-70 kbar, and 1030-1230 °C and 50-63 kbar, respectively. The Muskox xenoliths differ from xenoliths in the neighboring and contemporaneous Jericho kimberlite by their higher levels of depletion, the presence of a shallow zone of metasomatism in the spinel peridotite field, a higher proportion of pyroxenites at the base of the mantle column, higher Cr2O3 in all pyroxenite minerals, and weaker deformation in the Muskox mantle. We interpret these contrasts as representing small-scale heterogeneities in the bulk composition of the mantle, as well as the local effects of interaction between metasomatizing fluid and mantle wall rocks. We suggest that asthenosphere-derived pre-kimberlitic melts and fluids percolated less effectively through the less permeable Muskox mantle, resulting in lower degrees of hydrous weakening, strain, and fertilization of the peridotitic mantle. Fluids tended to concentrate and pool in the deep mantle, causing partial melting and formation of abundant pyroxenites.
Abstract: Kimberlite magmas, the primary source of diamonds, have many features indicative of explosive eruptions and high volatile contents. The main approaches used to establish exsolution of fluid during magma ascent include theoretical modeling and experimental estimates of volatile solubility in kimberlite-like melts. Both approaches are hampered by the poorly constrained composition of kimberlite melts. Resorption features on diamonds are very sensitive to the presence and composition of the kimberlite fluid as well as to temperature and pressure. Here, we use direct evidence from diamond resorption features as a new method for investigating the parameters of fluid exsolution. The method is based on experimental reproduction of diamond resorption in kimberlite melts with and without an exsolved fluid phase. We studied 802 diamonds from two kimberlites (BK1 and AK15) from the Orapa cluster, Botswana. Samples from the BK1 pipe include three lithologies: two coherent kimberlites (CK-A and CK-B) and a pyroclastic kimberlite (massive volcaniclastic kimberlite, MVK). The known depth of diamond samples in each kimberlite lithology allows us to demonstrate an increase in the intensity of kimberlite-induced resorption with depth of diamond recovery in the drill holes. Each kimberlite lithology has a different proportion of diamonds with kimberlite-induced resorption, which is unique in style in each lithology: glossy surfaces in MVK due to reaction with C-O-H fluid, rough corroded surfaces in CK-B due to reaction with volatile-undersaturated melt, and a combination of glossy surfaces with corroded features in CK-A due to an overprint of melt resorption after fluid resorption. Both diamond resorption and kimberlite textures in the BK1 kimberlite show evidence of fluid exsolution only in CK-A and MVK lithologies, but no fluid presence in CK-B. The observed diamond resorption features may be controlled by (1) a temporary separation of the rising magma column into a bubble-rich head and bubble-poor volatile-depleted tail and (2) fluid exsolution at depths greater than decompressional degassing. We discuss how the depth of fluid exsolution from kimberlite melt may affect the diamond grade and the resorption of diamond populations in a kimberlite.
Abstract: When carbonate-rich and silicate rocks are juxtaposed at high subsolidus temperature, their contrasting elemental chemical potentials trigger metasomatism. Kimberlites in contact with felsic-to-mafic rocks should theoretically develop skarn alteration, replacing both the wall rocks and magmatic rocks. Although some kimberlites are well exposed from mining, metasomatic effects in them are difficult to isolate because of the common presence of marginal country rock breccias and assimilated country rock xenoliths. The volatilerich nature of kimberlite melts and faulting prior to the emplacement results in country rock brecciation and incorporation of as much as 70% xenoliths in kimberlite. We discuss several examples of mineralogical, textural and chemical zonation at contacts between felsic-to-mafic xenoliths, in-situ country rocks and kimberlites (Renard, Gahcho Kue, Snap Lake and Orapa). The subsolidus skarn reactions are preceded by magmatic assimilation. It partially melts feldspars and forms diopside and phlogopite coronas on xenoliths. To distinguish between incorporation and assimilation of xenoliths and contact metasomatism, we employed an improved isocon analysis that enables estimation of metasomatic contributions to geochemical diversity. Skarn reactions replace the original kimberlite minerals with serpentine, phlogopite, hydrogarnet, while xenoliths are replaced by serpentine, clinopyroxene, carbonate, chlorite, and pectolite. If the mode of felsic-to-mafic xenoliths exceeds 30%, the textures and the mineralogy of the kimberlite altered by assimilation and skarn reactions may resemble those of the Kimberly-type pyroclastic kimberlite (KPK). The distinct mineralogy of the KPK interclast matrix, the correlation between xenolith modes and the kimberlite texture, the spatial distribution of KPK in Renard and Gahcho Kue kimberlites indicate the principal role of crustal xenoliths in the KPK formation. Our data suggest that metasomatic recrystallization of kimberlites is more widespread than previously recognized, but is complex and accompanied by xenolith assimilation.
Abstract: Peridotite xenoliths from the Cretaceous Chidliak kimberlite province (SE Baffin Island, Canada) were recently studied by Kopylova et al. (2019). Here, we focus on rare textures, with orthopyroxene grains invariably rimmed by 3-20??m coronas of clinopyroxene, while all clinopyroxenes are rimmed by equally thin monticellite coronas. Thicker, 0.1-0.5?mm texturally equilibrated clinopyroxene also mantles garnet, and there is a gradual transition from micron- to millimeter-thick clinopyroxene mantles. We investigated the origin of these rarely preserved textures using major and trace element zoning in minerals, and measured and reconstructed bulk compositions of xenoliths. Fluxes of major elements were identified based on the conserved element ratios while accounting for the closure effect due to normalization of bulk compositions to 100%. Ca dominates the absolute elemental gain, expressed in moles per 1000?mol of Fe. The observed mineralogical and compositional changes are associated with the significant metasomatic removal of Na (70% of its budget) Al, and Cr (35% loss), minor removal of Si, Mn, Mg and Ni and the gain of Ca (~ 20%), Ti, K and incompatible trace elements. The metasomatic fluid addition beneath Chidliak was likely below 10%. The fluid was very enriched and fractionated resembling volatile-rich low-degree melts like carbonatites or kimberlites. The Chidliak peridotites were affected by "“carbonation freezing", i.e. immobilization of a carbonate-rich metasomatic agent via reactions with pyroxenes. Clinopyroxene and monticellite coronas formed in decarbonation reactions, whereby ephemeral carbonatitic fluid readily gave away Ca to silicate minerals and exsolved CO2. Chidliak peridotites highlight that it would be deceptive to imagine "carbonated peridotites" storing carbon in a normal assemblage of peridotite plus carbonate. "Carbonated peridotites" are coarse peridotites with elevated modes of clinopyroxene, garnet and olivine, and with thin rims of calcic silicate minerals storing incompatible elements. The CO2-rich magmatism on cratons and the match between the temporal Ca addition to the cratonic mantle and the observed fluxes from the carbonate-rich metasomatism underscores the importance of the latter process in shaping up the lithospheric mantle and its melts.
Nature, doi.org/101038/ s41586-021-03395-5 5p. Pdf
Canada, Northwest Territories
craton
Abstract: Cratons are Earth’s ancient continental land masses that remain stable for billions of years. The mantle roots of cratons are renowned as being long-lived, stable features of Earth’s continents, but there is also evidence of their disruption in the recent1,2,3,4,5,6 and more distant7,8,9 past. Despite periods of lithospheric thinning during the Proterozoic and Phanerozoic eons, the lithosphere beneath many cratons seems to always ‘heal’, returning to a thickness of 150 to 200 kilometres10,11,12; similar lithospheric thicknesses are thought to have existed since Archaean times3,13,14,15. Although numerous studies have focused on the mechanism for lithospheric destruction2,5,13,16,17,18,19, the mechanisms that recratonize the lithosphere beneath cratons and thus sustain them are not well understood. Here we study kimberlite-borne mantle xenoliths and seismology across a transect of the cratonic lithosphere of Arctic Canada, which includes a region affected by the Mackenzie plume event 1.27 billion years ago20. We demonstrate the important role of plume upwelling in the destruction and recratonization of roughly 200-kilometre-thick cratonic lithospheric mantle in the northern portion of the Slave craton. Using numerical modelling, we show how new, buoyant melt residues produced by the Mackenzie plume event are captured in a region of thinned lithosphere between two thick cratonic blocks. Our results identify a process by which cratons heal and return to their original lithospheric thickness after substantial disruption of their roots. This process may be widespread in the history of cratons and may contribute to how cratonic mantle becomes a patchwork of mantle peridotites of different age and origin.
Abstract: The study reports petrography, bulk major and trace element compositions of lamprophyric Devonian dykes in three areas of the Kola Alkaline Carbonatite Province (N Europe). Dykes in one of these areas, Kandalaksha, are not associated with a massif, while dykes in Kandaguba and Turij Mys occur adjacent (< 5 km) to coeval central multiphase ultramafic alkaline?carbonatitic massifs. Kandalaksha dyke series consists of aillikites - phlogopite carbonatites and monchiquites. Kandaguba dykes range from monchiquites to nephelinites and phonolites; Turij Mys dykes represent alnöites, monchiquites, foidites, turjaites and carbonatites. Some dykes show extreme mineralogical and textural heterogeneity and layering we ascribe to fluid separation and crystal cumulation. Melt evolution of the dykes was modelled with Rhyolite-MELTS and compared with the observed order and products of the crystallization. Our results suggest that the studied rocks were related by fractional crystallization and liquid immiscibility. Primitive melts of aillikites or olivine melanephelinites initially evolved at P = 1.5-0.8 GPa without a SiO2 increase due to abundant clinopyroxene crystallization controlled by the CO2-rich fluid. At 1-1.1 GPa the Turij Mys melts separated immiscible carbonatite melt, which subsequently exsolved late carbonate-rich fluids extremely rich in trace elements. Kandaguba and Turij Mys melts continued to fractionate at lower pressures in the presence of hydrous fluid to the more evolved nephelinite and phonolite melts. The studied dykes highlight the critical role of the parent magma chamber in crystal fractionation and magma diversification. The Kandalaksha dykes may represent a carbonatite - ultramafic lamprophyre association, which fractionated at 45-20 km in narrow dykes on ascent to the surface and could not get more evolved than monchiquite. In contrast, connections of Kandaguba and Turij Mys dykes to their massif magma chambers ensured the sufficient time for fractionation, ascent and a polybaric evolution. This longevity generated more evolved rock types with the higher alkalinity and an immiscible separation of carbonatites.
Contribution to Mineralogy and Petrology, Vol. 1777, 2, 10.1007/s00410-021-01880-8
Africa, South Africa
deposit - Lace
Abstract: We studied diamond inclusions in the 133 Ma Lace kimberlite of the Kroonstad Group II kimberlite cluster (Kaapvaal craton) to compare them to diamonds beneath the adjacent coeval Voorspoed kimberlite. The studied 288 Lace diamonds are mostly colorless dodecahedral Type IaAB. Based on diamond inclusions (DI), 38 Lace diamonds were classified as eclogitic (44%, 19 samples), peridotitic (35%, 15 samples), and websteritic (9%, 4 samples). The diamonds formed from mantle carbon (?13C?=?? 9.1 to ? 2.5 ‰ for 18 samples), with the exception of one eclogitic diamond (?13C?=?? 19.2 ‰). A rare zircon inclusion provides age constraints for the Lace eclogite protolith at 3.2?±?0.4 Ga (Lu-Hf model age) and Lace eclogite diamond formation at 188?±?37 Ma (U-Pb age). The eclogite protolith age suggests its formation contemporaneous with the lower crustal magmatism and metamorphism in the Central Kaapvaal craton, complementary to the tonalite-trondhjemite-granodiorite magmatism in the region and synchronous with the consolidation of the Eastern Kaapvaal Block. Two distinct kinds of eclogites are found to host Lace diamonds, (1) Fe-rich eclogites located at 160-190 km, and (2) more calcic-magnesian eclogites with mineral compositions identical to websteritic DIs, that derive from shallower lithospheric depths. Various thermobarometric methods applied to Lace diamonds and DIs constrain the Lace geotherm as reflecting a surface heat flow below or equal to 38 mW/m2 and a lithosphere thickness of at least 220 km, at the time of kimberlite eruption. These thermal parameters demonstrate an excellent match between the thermal state of the Voorspoed and Lace mantle segments that persisted from the Archean to Cretaceous times. The Lace peridotitic-to-eclogitic diamond ratio (5/4) does not differ much from the Voorspoed DI ratio (6/4), but a hot and spatially restricted carbonatitic metasomatism event affected the Voorspoed peridotitic mantle to create the majority of Voorspoed diamonds. The contrast in the mineralogy of DIs in Lace and Voorspoed diamonds highlights the very local (ca. 10 km) extent of the metasomatism and heating, as well as the variability of the diamond-forming processes at the same spatial scale.
Geological Society of London Special Publication 513, pp. 179-207.
India
minette
Abstract: The lamproites and kimberlites are well known from the Eastern Bastar Craton, Central India. However, a Proterozoic lamprophyre dyke is discussed here, from the Western Bastar Craton (WBC). The field geology, petrographic, mineralogical and whole-rock and in-situ trace element geochemistry of biotite are described to understand the petrogenesis and lithospheric evolution in the WBC. The Thanewasna lamprophyre (TL) is undeformed and unmetamorphosed, intruded into c. 2.5 Ga charnockite and metagabbro but closely associated with c. 1.62 Ga undeformed Mul granite. The TL has a characteristic porphyritic texture, dominated by phenocrysts of biotite, microphenocryst of amphibole, clinopyroxene and a groundmass controlled by feldspar. Mineral chemistry of biotite and amphibole suggest a calc-alkaline (CAL) type, and pyroxene chemistry reveals an orogenic setting. The TL is characterized by high SiO2 and low TiO2, MgO, Ni and Cr, consistent with its subcontinental lithospheric origin. The presence of crustal xenolith and ocelli texture followed by observed variations in Th/Yb, Hf/Sm, La/Nb, Ta/La, Nb/Yb, Ba/Nb indicate substantial crustal contamination. Whole-rock and in-situ biotite analysis by laser ablation inductively coupled plasma mass spectrometry show low concentrations of Ni (30-50 ppm) and Cr (70-150 ppm), pointing to the parental magma evolved nature. Enrichment in H2O, reflected in magmatic mica dominance, combined with high large ion lithophile element, Th/Yb ratios, and striking negative Nb-Ta anomalies in trace element patterns, is consistent with a source that was metasomatized by hydrous fluids corresponding to those generated by subduction-related processes. Significant Zr-Hf and Ti anomalies in the primitive mantle normalized multi-element plots and the rare earth element pattern of the TL, similar to the global CAL average trend, including Eastern Dharwar Craton lamprophyres. Our findings provide substantial petrological and geochemical constraints on petrogenesis and geodynamics. However, the geodynamic trigger that generated CAL magmatism and its role in Cu-Au metallogeny in the WBC, Central India, is presently indistinct in the absence of isotopic studies. Nevertheless, the lamprophyre dyke is emplaced close to the Cu-(Au) deposit at Thanewasna.
Tuffisitic kimberlite from Eastern Dharwar craton, Undraldoddi area, Raichur District, Karnataka, India.
Proceedings of the 10th. International Kimberlite Conference, Vol. 2, Special Issue of the Journal of the Geological Society of India,, Vol. 2, pp. 109-128.
Petrology of P-5 and P-13 kimberlites from Lattavaram kimberlite cluster, Wajrakarur kimberlite field, Andhra Pradesh, India: reclassification as lamproites.
Proceedings of the 10th. International Kimberlite Conference, Vol. 1, Special Issue of the Journal of the Geological Society of India,, Vol. 1, pp. 183-194.
Abstract: Petrographic, mineral chemical and whole-rock geochemical characteristics of two newly discovered lamproitic dykes (Dyke 1 and Dyke 2) from the Sidhi Gneissic Complex (SGC), Central India are presented here. Both these dykes have almost similar sequence of mineral-textural patterns indicative of: (1) an early cumulate forming event in a deeper magma chamber where megacrystic/large size phenocrysts of phlogopites have crystallized along with subordinate amount of olivine and clinopyroxene; (2) crystallization at shallow crustal levels promoted fine-grained phlogopite, K-feldspar, calcite and Fe-Ti oxides in the groundmass; (3) dyke emplacement related quench texture (plumose K-feldspar, acicular phlogopites) and finally (4) post emplacement autometasomatism by hydrothermal fluids which percolated as micro-veins and altered the mafic phases. Phlogopite phenocrysts often display resorption textures together with growth zoning indicating that during their crystallization equilibrium at the crystal-melt interface fluctuated multiple times probably due to incremental addition or chaotic dynamic self mixing of the lamproitic magma. Carbonate aggregates as late stage melt segregation are common in both these dykes, however their micro-xenolithic forms suggest that assimilation with a plutonic carbonatite body also played a key role in enhancing the carbonatitic nature of these dykes. Geochemically both dykes are ultrapotassic (K2O/Na2O: 3.0 -9.4) with low CaO, Al2O3 and Na2O content and high SiO2 (53.3 -55.6 wt.%) and K2O/Al2O3 ratio (0.51 -0.89) characterizing them as high-silica lamproites. Inspite of these similarities, many other features indicate that both these dykes have evolved independently from two distinct magmas. In dyke 1, phlogopite composition has evolved towards the minette trend (Al-enrichment) from a differentiated parental magma having low MgO, Ni and Cr content; whereas in dyke 2, phlogopite composition shows an evolutionary affinity towards the lamproite trend (Al-depletion) and crystallized from a more primitive magma having high MgO, Ni and Cr content. Whole-rock trace-elements signatures like enriched LREE, LILE, negative Nb-Ta and positive Pb anomalies; high Rb/Sr, Th/La, Ba/Nb, and low Ba/Rb, Sm/La, Nb/U ratios in both dykes indicate that their parental magmas were sourced from a subduction modified garnet facies mantle containing phlogopite. From various evidences it is proposed that the petrogenesis of studied lamproitic dykes stand out to be an example for the lamproite magma which attained a carbonatitic character and undergone diverse chemical evolution in response to parental melt composition, storage at deep crustal level and autometasomatism.
Abstract: In this contribution, we present detailed field, petrography, mineral chemistry, and geochemistry of newly identified high-Si high-Mg metavolcanic rocks from the southern part of the ~3.3 Ga Holenarsipur greenstone belt in the western Dharwar craton, India. The rocks occur as conformable bands that were interleaved with the mafic-ultramafic units. The entire volcanic package exhibits uniform foliation pattern, and metamorphosed under greenschist to low grade amphibolite facies conditions. The rocks are extremely fine grained and exhibit relict primary igneous textures. They are composed of orthopyroxene and clinopyroxene phenocrysts with serpentine, talc, and amphibole (altered clinopyroxene). Cr-spinel, rutile, ilmenite, and apatite occur as disseminated minute grains in the groundmass. The mineralogical composition and the geochemical signatures comprising of high SiO2 (~53 wt. %), Mg# (~83), low TiO2 (~0.18 wt. %), and higher than chondritic Al2O3/TiO2 ratio (~26), reversely fractionated heavy rare earth elements (REE) (GdN/YbN ~ 0.8), resulting in concave-up patterns, and positive Zr anomaly, typically resembled with the Phanerozoic boninites. Depletion in the high field strength elements Nb, and Ti relative to Th and the REE in a primitive mantle normalized trace element variation diagram, cannot account for contamination by pre-existing Mesoarchean continental crust present in the study area. The trace element attributes instead suggest an intraoceanic subduction-related tectonic setting for the genesis of these rocks. Accordingly, the Holenarsipur high-Si high-Mg metavolcanic rocks have been identified as boninites. It importantly indicates that the geodynamic process involved in the generation of Archean boninites, was perhaps not significantly different from the widely recognized two-stage melt generation process that produced the Phanerozoic boninites, and hence provides compelling evidence for the onset of Phanerozoic type plate tectonic processes by at least ~3.3 Ga, in the Earth’s evolutionary history.
Abstract: Madawara ultramafic complex (MUC) in the southern part of Bundelkhand Craton, Central India comprises peridotite, olivine pyroxenite, pyroxenite, gabbro, and diorite. Coarse?grained olivine, clinopyroxene (Cpx), amphibole (Amp), Al?chromite, Fe?chromite, and magnetite with rare orthopyroxene (Opx) are common minerals in peridotite. Chromites are usually coarse?grained euhedral found as disseminated crystals in the olivine matrix showing both homogeneous and zoned texture. Al?chromite, primarily characterizes Cr?spinels and its subsequent fluid activity and alteration can result in the formation of Fe?chromite, chrome magnetite, and magnetite. Mineral chemistry data suggest that Al?chromite is characterized by moderately high Cr2O3 (38.16-51.52 wt.%) and Fe2O3 (3.22-14.51 wt.%) and low Al2O3 (10.63-21.87 wt.%), MgO (1.71-4.92 wt.%), and TiO2 (0.22-0.67 wt.%), whereas the homogeneous Fe?chromite type is characterized by high Fe2O3 (25.54-47.60 wt.%), moderately low Cr2O3 (19.56-37.90 wt.%), and very low Al2O3 (0.06-1.53 wt.%). Subsequent alteration of Al?chromite and Fe?chromite leads to formation of Cr?magnetite and magnetite. The Cr# of Al?chromite varies from 55.12 to 76.48 and ?Fe3+# from 8 to 19, whereas the ferrian chromite has high Cr# varying from 94.27 to 99.53 while its ?Fe3+# varies from 38 to 70. As a whole, the primary Al?chromite shows low Al2O3, TiO2 contents, and high Fe#, Cr# values. Olivines have forsterite ranging from 75.96% to 77.59%. The bulk?rock geochemistry shows continental arc geochemical affinities indicated by the high concentration of large?ion lithophile elements and U, Th relative to the low concentration of high?field strength elements. These petrological and mineralogical as well as primary Al?chromite compositions plotted in different discrimination diagrams suggest an arc environment that is similar to Alaskan?type intrusion.
Journal of Raman Spectroscopy, Vol. 48, 11, pp. 1566-1573.
Russia
UHP - Kokchetav
Abstract: CO2-bearing fluid inclusions coexisting with diamonds were identified in zircons from diamondiferous gneiss in the Kokchetav Massif. This discovery provides evidence for the presence of CO2 in UHP fluids and diamond formation in moderately oxidized conditions in the Kokchetav gneiss. Fluid and multiphase solid inclusions coexisting in zircons represent immiscible melt and fluid captured close to the peak metamorphic conditions for the Kokchetav UHP gneiss. Most of CO2-bearing inclusions are CO2+H2O mixtures except for some cases when they also contain daughter phases (e.g. muscovite, calcite and quartz) tracing the presence of aqueous and solute-rich fluids at different phases of UHP metamorphism. Decrease of pressure and temperature may have been responsible for the reduction of solutes in the CO2-bearing fluid. The lack of CO2-bearing inclusions in garnet porphyroblasts from diamond-bearing gneiss, as well as the common coexistence of aqueous CO2-bearing inclusions with calcite, testify that most likely all CO2 in fluid was consumed by the calcite-forming reaction and hydrous melt was the only remaining growth medium during retrograde metamorphism of the Kokchetav UHPM gneisses. Neither K-cymrite nor kokchetavite was identified among daughter phases in the hydrous melt inclusions in garnet, which indicates that they hardly could originate in a metapelitic system.
Abstract: Clear evidence for subduction-induced metamorphism, and thus the operation of plate tectonics on the ancient Earth has been lacking. Theoretical calculations indicate that we may have been looking for something that cannot exist.
Earth and Planetary Science Letters, Vol. 494, pp. 42-49.
Mantle
geodynamics
Abstract: The geodynamic regime of the early Earth remains elusive, with so far proposed hypotheses ranging from stagnant lid convection to rapid plate tectonics. Available geological data are severely limited for the first two billion years of the Earth's history, and this scarcity of relevant data is often compounded by the nonuniqueness of interpretation. Here we propose that the samarium-neodymium isotope evolution, which has been suggested to be consistent with stagnant lid convection in the early Earth, may be better understood as the result of rapid crustal growth and extensive crustal recycling. We delineate the permissible scenario of crustal evolution through geochemical box modeling with a Monte Carlo sampling of the model parameter space, and our results suggest that the net growth of continental crust was complete by the end of the Hadean and that the rate of crustal recycling could have been as high as kg Gyr?1 at that time and has gradually decreased since then. Such crustal evolution yields a specific prediction for the present-day distribution of crustal formation ages, which is shown to be in remarkable agreement with a recent estimate based on the global compilation of zircon age data. The mode of subsolidus mantle convection after the putative magma ocean is probably plate tectonics, but its style could have been very different from that of contemporary plate tectonics, characterized by more voluminous magmatism and more destructive subduction.
Abstract: We present a global compilation of major element, as well as Re-Os isotope, data on mantle xenoliths from continental lithosphere to constrain the secular evolution of mantle depletion since the early Archean. Whereas a temporal dichotomy in the degree of mantle depletion has long been recognized in previous regional studies of mantle xenoliths, this global compilation reveals, for the first time, a smooth secular trend in mantle depletion, which is in remarkable agreement with what is expected from the secular cooling of the ambient mantle as inferred from the petrology of non-arc basalts. Depleted mantle now composing continental lithosphere is likely to have been originally formed beneath mid-ocean ridges or similar spreading environments, and a greater degree of depletion in the past can be seen as a corollary of the secular cooling of the mantle.
Abstract: Earth is so far the only planet that exhibits plate tectonics, and along with the right heliocentric distance and the presence of surface water, plate tectonics is among necessary conditions for a habitable planet. Yet, the physics of this particular style of mantle convection is poorly understood, creating a substantial bottleneck in developing the general theory of planetary evolution. As plate tectonics is characterized by the subduction of oceanic lithosphere, a better understanding of the oceanic upper mantle could potentially help to break this stalemate. In this review, I summarize available theoretical, observational, and experimental constraints on the evolution of the oceanic upper mantle and its rheology, place the study of the oceanic upper mantle in the big picture of Earth evolution, and provide some suggestions for future research in relevant disciplines, including marine geophysics and computational geodynamics.
Abstract: Continental lithospheric mantle (CLM) may have been built from subducted slabs, but the apparent lack of concurrent oceanic crust in CLM, known as the mass imbalance problem, remains unresolved. Here, we present a simple dynamic model to evaluate the likelihood of losing dense eclogitized oceanic crust from CLM by gravitational instability. Our model allowed us to assess the long-term evolution of such crust removal, based on how thermal and viscosity profiles change over time across the continental lithosphere. We found that the oceanic crust incorporated early into CLM can quickly escape to the asthenosphere, whereas that incorporated after a certain age would be preserved in CLM. This study provides a plausible explanation for the mass imbalance problem posed by the oceanic ridge origin hypothesis of CLM and points to the significance of preservation bias inherent to the studies of cratonic diamonds.
Earth and Planetary Science Letters, in press available 8p. Pdf
Mantle
tectonics
Abstract: Deep mantle plumes imaged by seismic tomography have much larger radii (?400 km) than predicted by conventional geodynamic models (?100 km). Plume buoyancy fluxes estimated from surface topography concur with narrow plumes with low viscosities expected from their high temperatures. If plumes are thick as imaged by tomography, buoyancy flux estimates may require very viscous or thermochemical plumes. Here we assess the dynamical plausibility of an alternative model, a ponding plume, which has been suggested to explain thick plumes as well as buoyancy fluxes estimated from surface topography. In the ponding plume model, a thick conduit in the lower mantle narrows significantly after passing through the mantle transition zone, below which excess material from the thick lower-mantle plume, which cannot be accommodated by the narrow upper-mantle plume, spreads laterally. Such excess material in the mid-mantle, however, should still manifest itself in surface topography, the amplitude of which can be quantified via topography kernels. We find that the ponding of a purely thermal plume would lead to unrealistic excess topography, with the scale of ponding material large enough to be detected by seismic tomography. If mantle plumes are as thick as indicated by seismic tomography, it appears to be necessary to deviate from either conventional temperature-dependent viscosity or the assumption of purely thermal origins.
Abstract: Hf isotope data for zircons and whole-rocks from lower crustal mafic granulite and pyroxenite xenoliths from NW Russia are presented together with the results of U-Pb zircon dating, Sm-Nd and Rb-Sr isotopic compositions of bulk-rocks and minerals, and trace element compositions of minerals. Most zircons preserve a record of only the youngest metamorphic events, but a few Grt-granulite xenoliths retain Archean magmatic zircons from their protolith. Metamorphic zircons have highly variable ?Hf(t) values from -25 to -4. The least radiogenic zircons were formed by recrystallization of primary magmatic Archean zircons. Zircons with the most radiogenic ?Hf grew before garnet or were contemporaneous with its formation. Zircons with ?Hf(t) from -15 to -9 formed by various mechanisms, including recrystallization of pre-existing metamorphic zircons, subsolidus growth in the presence of garnet and exsolution from rutile. They inherited their Hf isotopic composition from clinopyroxene, pargasite, rutile and earlier-formed zircon that had equilibrated with garnet. Subsolidus zircons were formed in response to a major change in mineral association (i.e. garnet- and zircon-producing reactions including partial melting). Recrystallized zircons date the onset of high-temperature conditions without a major change in mineral association. Age data for metamorphic zircons fall into five groups: >1•91 Ga, 1•81-1•86 Ga, 1•74-1•77 Ga, 1•64-1•67 Ga and <1•6 Ga. Most ages correlate with metamorphic events in the regional upper crust superimposed onto rocks of the Belomorian belt during formation of the Lapland Granulite Belt. Zircon formation and resetting at 1•64-1•67 Ga significantly postdates Lapland-Kola orogenic events and may relate to the onset of Mesoproterozoic rifting. The youngest ages (1•6-1•3 Ga) correspond to an event that affected only a few grains in some samples and can be explained by interaction with a localized fluid. The observed garnet-granulite associations were formed at 1•83 Ga in Arkhangelsk xenoliths and 1•74-1•76 Ga in most Kola xenoliths. By the end of the Lapland-Kola orogeny, the rocks were already assembled in the lower crust. However, no addition of juvenile material has been detected and preservation of pre-Lapland-Kola metamorphic zircon indicates that some xenoliths represent an older lower crust. Granulites, pyroxenites and Phl-rich rocks have a common metamorphic history since at least c. 1•75 Ga. At about 1•64 Ga metasomatic introduction of phlogopite took place; however, this was only one of several phlogopite-forming events in the lower crust.
Abstract: Hf isotope data for zircons and whole-rocks from lower crustal mafic granulite and pyroxenite xenoliths from NW Russia are presented together with the results of U-Pb zircon dating, Sm-Nd and Rb-Sr isotopic compositions of bulk-rocks and minerals, and trace element compositions of minerals. Most zircons preserve a record of only the youngest metamorphic events, but a few Grt-granulite xenoliths retain Archean magmatic zircons from their protolith. Metamorphic zircons have highly variable ?Hf(t) values from -25 to -4. The least radiogenic zircons were formed by recrystallization of primary magmatic Archean zircons. Zircons with the most radiogenic ?Hf grew before garnet or were contemporaneous with its formation. Zircons with ?Hf(t) from -15 to -9 formed by various mechanisms, including recrystallization of pre-existing metamorphic zircons, subsolidus growth in the presence of garnet and exsolution from rutile. They inherited their Hf isotopic composition from clinopyroxene, pargasite, rutile and earlier-formed zircon that had equilibrated with garnet. Subsolidus zircons were formed in response to a major change in mineral association (i.e. garnet- and zircon-producing reactions including partial melting). Recrystallized zircons date the onset of high-temperature conditions without a major change in mineral association. Age data for metamorphic zircons fall into five groups: >1•91 Ga, 1•81-1•86 Ga, 1•74-1•77 Ga, 1•64-1•67 Ga and <1•6 Ga. Most ages correlate with metamorphic events in the regional upper crust superimposed onto rocks of the Belomorian belt during formation of the Lapland Granulite Belt. Zircon formation and resetting at 1•64-1•67 Ga significantly postdates Lapland-Kola orogenic events and may relate to the onset of Mesoproterozoic rifting. The youngest ages (1•6-1•3 Ga) correspond to an event that affected only a few grains in some samples and can be explained by interaction with a localized fluid. The observed garnet-granulite associations were formed at 1•83 Ga in Arkhangelsk xenoliths and 1•74-1•76 Ga in most Kola xenoliths. By the end of the Lapland-Kola orogeny, the rocks were already assembled in the lower crust. However, no addition of juvenile material has been detected and preservation of pre-Lapland-Kola metamorphic zircon indicates that some xenoliths represent an older lower crust. Granulites, pyroxenites and Phl-rich rocks have a common metamorphic history since at least c. 1•75 Ga. At about 1•64 Ga metasomatic introduction of phlogopite took place; however, this was only one of several phlogopite-forming events in the lower crust.
Zircon trace element characteristics and ages in granulite xenoliths: a key to understanding the age and origin of the lower crust, Arkhangelsk kimberlite province, Russia.
Contributions to Mineralogy and Petrology, Vol. 167, pp. 973-980.
Journal of Metamorphic Geology, in press available
Mantle
Craton
Abstract: The Proterozoic belts that occur along the margins of the West Australian Craton, as well as those in intraplate settings, generally share similar geological histories that suggest a common plate-margin driver for orogeny. However, the thermal drivers for intraplate orogenesis are generally more poorly understood. The Mutherbukin Tectonic Event records a protracted period of Mesoproterozoic reworking of the Capricorn Orogen and offers significant insight into both the tectonic drivers and heat sources of long-lived intraplate orogens. Mineral assemblages and tectonic fabrics related to this event occur within a 50 km-wide fault-bound corridor in the central part of the Gascoyne Province in Western Australia. This zone preserves a crustal profile, with greenschist facies rocks in the north grading to upper amphibolite facies rocks in the south. The P- T-t evolution of 13 samples from 10 localities across the Mutherbukin Zone is investigated using phase equilibria modelling integrated with in situ U-Pb monazite and zircon geochronology. Garnet chemistry from selected samples is used to further refine the P-T history and shows that the dominant events recorded in this zone are prolonged D1 transpression between c. 1320 and 1270 Ma, followed by D2 transtension from c. 1210 to 1170 Ma. Peak metamorphic conditions in the mid-crust reached >650 °C and 4.4-7 kbar at c. 1210-1200 Ma. Most samples record a single clockwise P-T evolution during this event, although some samples might have experienced multiple perturbations. The heat source for metamorphism was primarily conductive heating of radiogenic mid- and upper crust, derived from earlier crustal differentiation events. This crust was thickened during D1 transpression, although the thermal effects persisted longer than the deformation event. Peak metamorphism was terminated by D2 transtension at c. 1210 Ma, with subsequent cooling driven by thinning of the radiogenic crust. The coincidence of a sedimentary basin acting as a thermal lid and a highly radiogenic mid-crustal batholith restricted to the Mutherbukin Zone accounts for reworking being confined to a discrete crustal corridor. Our results show that radiogenic regions in the shallow to mid crust can elevate the thermal gradient and localize deformation, causing the crust to be more responsive to far-field stresses. The Mutherbukin Tectonic Event in the Capricorn Orogen was synchronous with numerous Mesoproterozoic events around the West Australian Craton, suggesting that thick cratonic roots play an important role in propagating stresses generated at distant plate boundaries.
Korikovsky, S., Kotov, A., Salnikova, E., Aranovich, L., Korpechkov, D., Yakovleva, S., Tolmacheva, E., Anisimova, I.
The age of the protolith of metamorphic rocks in the southeastern Lapland granulite belt, southern Kola Peninsula: correlation with the Belomorian mobile belt in the context of the problem of Archean eclogites.
Russian Geology and Geophysics, Vol. 59, 11, pp. 1389-1409.
Russia
craton
Abstract: Precambrian cratons cover about 70% of the total continental area. According to a large volume of geomorphological, geological, paleontological, and other data for the Pliocene and Pleistocene, these cratons have experienced a crustal uplift from 100-200 m to 1000-1500 m, commonly called the recent or Neotectonic uplift. Shortening of the Precambrian crust terminated half a billion years ago or earlier, and its uplift could not have been produced by this mechanism. According to the main models of dynamic topography in the mantle, the distribution of displacements at the surface is quite different from that of the Neotectonic movements. According to seismic data, there is no magmatic underplating beneath most of the Precambrian cratons. In most of cratonic areas, the mantle lithosphere is very thick, which makes its recent delamination unlikely. Asthenospheric replacement of the lower part of the mantle lithosphere beneath the Precambrian cratons might have produced only a minor part of their Neotectonic uplifts. Since the above mechanisms cannot explain this phenomenon, the rock expansion in the crustal layer is supposed to be the main cause of the recent uplift of Precambrian cratons. This is supported by the strong lateral nonuniformity of the uplift, which indicates that expansion of rocks took place at a shallow depth. Expansion might have occurred in crustal rocks that emerged from the lower crust into the middle crust with lower pressure and temperature after the denudation of a thick layer of surface rocks. In the dry state, these rocks can remain metastable for a long time. However, rapid metamorphism accompanied by expansion of rocks can be caused by infiltration of hydrous fluids from the mantle. Analysis of phase diagrams for common crustal rocks demonstrates that this mechanism can explain the recent crustal uplift of Precambrian cratons.
Abstract: Neoarchean intraplate granitoid (2.61 Ga) and carbonatite magmatism are established in the Kursk block of Sarmatia in close spatial association. Alkaline pyroxenites, carbonatites, and syenites of the Dubravinskii complex are represented by two relatively large intrusions and a few small plutons. They underwent amphibolite facies metamorphism at about 2.07 Ga. The age of alkaline-carbonatite magmatism is 2.59 Ga according to SIMS isotope dating of zircon from syenites. The close age and spatial conjugation allow the Dubravinskii carbonatite complex to be considered to have formed in intraplate conditions. The mantle plume upwelling caused metasomatic alteration and consequent partial melting of the sublithospheric mantle and intrusion of enriched magmas into the crust. Contamination of alkaline mantle melts in the crust by Archean TTGs caused the formation of syenites melts in the form of dykes that cutting through pyroxenites and carbonatites.
Pure and Applied Geophysics, Vol. 177, 8, pp. 3775-3795. pdf
Europe, Finland
geophysics - seismics
Abstract: The Kokkola-Kymi Deep Seismic Sounding profile crosses the Fennoscandian Shield in northwest-southeast (NW-SE) direction from Bothnian belt to Wiborg rapakivi batholith through Central Finland granitoid complex (CFGC). The 490-km refraction seismic line is perpendicular to the orogenic strike in Central Finland and entirely based on data from quarry blasts and road construction sites in years 2012 and 2013. The campaign resulted in 63 usable seismic record sections. The average perpendicular distance between these and the profile was 14 km. Tomographic velocity models were computed with JIVE3D program. The velocity fields of the tomographic models were used as starting points in the ray tracing modelling. Based on collected seismic sections a layer-cake model was prepared with the ray tracing package SEIS83. Along the profile, upper crust has an average thickness of 22 km average, and P-wave velocities (Vp) of 5.9-6.2 km/s near the surface, increasing downward to 6.25-6.40 km/s. The thickness of middle crust is 14 km below CFGC, 20 km in SE and 25 km in NW, but Vp ranges from 6.6 to 6.9 km/s in all parts. Lower crust has Vp values of 7.35-7.4 km/s and lithospheric mantle 8.2-8.25 km/s. Moho depth is 54 km in NW part, 63 km in the middle and 43 km in SW, yet a 55-km long section in the middle does not reveal an obvious Moho reflection. S-wave velocities vary from 3.4 km/s near the surface to 4.85 km/s in upper mantle, consistently with P-wave velocity variations. Results confirm the previously assumed high-velocity lower crust and depression of Moho in central Finland.
Jones, A.G., Plomerova, J., Korja, T., Sodoudi, F., Spakman, W.
Europe from the bottom up: a statistical examination of the central and northern European lithosphere asthenosphere boundary comparing seismological & EM
Abstract: Geochemical characterization including mineralogical measurements and kinetic testing was completed on samples from the Montviel carbonatite deposit, located in Quebec (Canada). Three main lithological units representing both waste and ore grades were sampled from drill core. A rare earth element (REE) concentrate was produced through a combination of gravity and magnetic separation. All samples were characterized using different mineralogical techniques (i.e., quantitative evaluation of minerals by scanning electron microscopy (QEMSCAN), X-ray diffraction (XRD), and scanning electron microscopy with X-ray microanalysis (SEM-EDS)) in order to quantify modal mineralogy, liberation, REE deportment and composition of REE-bearing phases. The REE concentrate was then submitted for kinetic testing (weathering cell) in order to investigate the REE leaching potential. The mineralogical results indicate that: (i) the main REE-bearing minerals in all samples are burbankite, kukharenkoite-Ce, monazite, and apatite; (ii) the samples are dominated by REE-free carbonates (i.e., calcite, ankerite, and siderite); and (iii) LREE is more abundant than HREE. Grades of REE minerals, sulfides and oxides are richer in the concentrate than in the host lithologies. The geochemical test results show that low concentrations of light REE are leached under kinetic testing conditions (8.8-139.6 ?g/L total light REE). These results are explained by a low reactivity of the REE-bearing carbonates in the kinetic testing conditions, low amounts of REE in solids, and by precipitation of secondary REE minerals.
Contributions to Mineralogy and Petrology, Vol. 177, 4. 10.1007/s00410-022-01910-z
Mantle
water
Abstract: Oxidized fluids in the subduction zone may convert polyvalent elements in the mantle to their higher valence states. The most abundant polyvalent element in the mantle is Fe, a significant part of which is contained in olivine as Fe2+. Results of the study of arc mantle xenoliths, in lab high-pressure-high-temperature experiments, and thermodynamic modeling have shown that at pressures of?~?50-2000 MPa and temperatures of 1000-1250 °C, well above the serpentine stability field, Fe2+ from olivine reacts with free aqueous fluid according to the following simplified reaction: 3Fe2SiO4?+?2H2O???3SiO2?+?2Fe3O4?+?2H2. The resulting ferric iron is preserved in spinel of a certain composition, (Mg,Fe2+)Fe3+2O4, whereas new high-Mg olivine, with magnesium number up to 96 in natural samples and 99.9 in experiments, forms in the reaction zone. SiO2 produced in the reaction either dissolves in the fluid or, with a small amount of water, reacts with olivine to form orthopyroxene as follows: (Mg,Fe)2SiO4?+?SiO2?=?(Mg,Fe)2Si2O6. The released H2 may decrease the oxidation state of polyvalent elements present in the fluid (e.g., S4+, S6+). Traces of high-temperature water-olivine interaction appear as swarms of fluid-spinel inclusions and are ubiquitous in olivine from ultramafic arc xenoliths. The described process is similar to serpentinization but occurs at higher pressure and temperature conditions and yields different reaction products. The reducing capacity of olivine is relatively low; however, given the large volume of mantle (and crustal) peridotites, the overall effect may be significant.
Abstract: Sulfide liquids that immiscibly separate from silicate melts in different magmatic processes accumulate chalcophile metals and may represent important sources of the metals in Earth's crust for the formation of ore deposits. Sulfide phases commonly found in some primitive mid-ocean ridge basalts (MORB) may support the occurrence of sulfide immiscibility in the crust without requiring magma contamination and/or extensive fractionation. However, the records of incipient sulfide melts in equilibrium with primitive high-Mg olivine and Cr-spinel are scarce. Sulfide globules in olivine phenocrysts in picritic rocks of MORB-affinity at Kamchatsky Mys (Eastern Kamchatka, Russia) represent a well-documented example of natural immiscibility in primitive oceanic magmas. Our study examines the conditions of silicate-sulfide immiscibility in these magmas by reporting high precision data on the compositions of Cr-spinel and silicate melt inclusions, hosted in Mg-rich olivine (86.9-90 mol% Fo), which also contain globules of magmatic sulfide melt. Major and trace element contents of reconstructed parental silicate melts, redox conditions (?QFM = +0.1 ± 0.16 (1?) log. units) and crystallization temperature (1200-1285 °C), as well as mantle potential temperatures (~1350 °C), correspond to typical MORB values. We show that nearly 50% of sulfur could be captured in daughter sulfide globules even in reheated melt inclusions, which could lead to a significant underestimation of sulfur content in reconstructed silicate melts. The saturation of these melts in sulfur appears to be unrelated to the effects of melt crystallization and crustal assimilation, so we discuss the reasons for the S variations in reconstructed melts and the influence of pressure and other parameters on the SCSS (Sulfur Content at Sulfide Saturation).
International Journal of Earth Sciences, in press available 17p.
Africa, Namibia
Alkaline rocks
Abstract: Rb-Sr whole-rock and mineral isotope data from nepheline syenite, tinguaite, and carbonatite samples of the Kalkfeld Complex within the Damaraland Alkaline Province, NW Namibia, indicate a date of 242?±?6.5 Ma. This is interpreted as the age of final magmatic crystallization in the complex. The geological position of the complex and the spatially close relationship to the Lower Cretaceous Etaneno Alkaline Complex document a repeated channeling of small-scale alkaline to carbonatite melt fractions along crustal fractures that served as pathways for the mantle-derived melts. This is in line with Triassic extensional tectonic activity described for the nearby Omaruru Lineament-Waterberg Fault system. The emplacement of the Kalkfeld Complex more than 100 Ma prior to the Paraná-Etendeka event and the emplacement of the Early Cretaceous Damaraland intrusive complexes excludes a genetic relationship to the Tristan Plume. The initial ?Sr-?Nd pairs of the Kalkfeld rocks are typical of younger African carbonatites and suggest a melt source, in which EM I and HIMU represent dominant components.
International Journal of Earth Sciences, Vol. 106, pp. 2797-2813.
Africa, Namibia
carbonatites
Abstract: Rb-Sr whole-rock and mineral isotope data from nepheline syenite, tinguaite, and carbonatite samples of the Kalkfeld Complex within the Damaraland Alkaline Province, NW Namibia, indicate a date of 242?±?6.5 Ma. This is interpreted as the age of final magmatic crystallization in the complex. The geological position of the complex and the spatially close relationship to the Lower Cretaceous Etaneno Alkaline Complex document a repeated channeling of small-scale alkaline to carbonatite melt fractions along crustal fractures that served as pathways for the mantle-derived melts. This is in line with Triassic extensional tectonic activity described for the nearby Omaruru Lineament-Waterberg Fault system. The emplacement of the Kalkfeld Complex more than 100 Ma prior to the Paraná-Etendeka event and the emplacement of the Early Cretaceous Damaraland intrusive complexes excludes a genetic relationship to the Tristan Plume. The initial ?Sr-?Nd pairs of the Kalkfeld rocks are typical of younger African carbonatites and suggest a melt source, in which EM I and HIMU represent dominant components.
International Journal of Earth Sciences, Vol. 106, 8, pp. 2797-2813.
Africa, Namibia
carbonatite
Abstract: Rb-Sr whole-rock and mineral isotope data from nepheline syenite, tinguaite, and carbonatite samples of the Kalkfeld Complex within the Damaraland Alkaline Province, NW Namibia, indicate a date of 242 ± 6.5 Ma. This is interpreted as the age of final magmatic crystallization in the complex. The geological position of the complex and the spatially close relationship to the Lower Cretaceous Etaneno Alkaline Complex document a repeated channeling of small-scale alkaline to carbonatite melt fractions along crustal fractures that served as pathways for the mantle-derived melts. This is in line with Triassic extensional tectonic activity described for the nearby Omaruru Lineament-Waterberg Fault system. The emplacement of the Kalkfeld Complex more than 100 Ma prior to the Paraná-Etendeka event and the emplacement of the Early Cretaceous Damaraland intrusive complexes excludes a genetic relationship to the Tristan Plume. The initial ?Sr-?Nd pairs of the Kalkfeld rocks are typical of younger African carbonatites and suggest a melt source, in which EM I and HIMU represent dominant components.
Abstract: The article reports basic design parameters of open pit mines of ALROSA, as well as criteria and factors that govern the choice of production capacity of an open pit diamond mine under conditions of permafrost. The analytical relations and tables to calculate open pit mine life are presented, and the influence of the rate of the downward advance of an open pit mine on its capacity is demonstrated. The authors formulate key provisions for a paragraph of the national standard of RF enabling systematization of approaches to optimization of open diamond mining parameters.
Garnet and or Spinel Bearing Pyroxenites in Alkaki Basalts Near Azrou Middle Atl|as, Morocco: Mantle Derived Alumin a Rich Xenoliths Related to the Ariegite Grospydite Trend.
Proceedings of Third International Kimberlite Conference, Vol. 2, PP. 179-189.
Abstract: Pyroxenites and garnet pyroxenites are mantle heterogeneities characterized by a lower solidus temperature than the enclosing peridotites; it follows that they are preferentially involved during magma genesis. Constraining their origin, composition, and the interactions they underwent during their subsequent evolution is therefore essential to discuss the sources of magmatism in a given area. Pyroxenites could represent either recycling of crustal rocks in mantle domains or mantle originated rocks (formed either by olivine consuming melt-rock reactions or by crystal fractionation). Petrological and geochemical (major and trace elements, Sr-Nd and O isotopes) features of xenoliths from various occurrences (French Massif-Central, Jordan, Morocco and Cameroon) show that these samples represent cumulates crystallized during melt percolation at mantle conditions. They formed in mantle domains at pressures of 1-2 GPa during post-collisional magmatism (possibly Hercynian for the French Massif-Central, and Panafrican for Morocco, Jordan and Cameroon). The thermal re-equilibration of lithospheric domains, typical of the late orogenic exhumation stages, is also recorded by the samples. Most of the samples display a metasomatic overprint that may be either inherited or likely linked to the recent volcanic activity that occurred in the investigated regions. The crystallization of pyroxenites during late orogenic events has implications for the subsequent evolution of the mantle domains. The presence of large amounts of mantle pyroxenites in old orogenic regions indeed imparts peculiar physical and chemical characteristics to these domains. Among others, the global solidus temperature of the whole lithospheric domain will be lowered; in turn, this implies that old orogenic regions are refertilized zones where magmatic activity would be enhanced.
Abstract: Boris Choubert was a strong supporter of Wegener's continental drift theory. In 1935, he published a very accurate fit of the circum-Atlantic continents, which was based on continental edges instead of coastlines; in the same paper, he interpreted the Palaeozoic belts as the result of horizontal movements of the Precambrian blocks; so, he greatly expanded the role of continental drift through time. This original and very prophetic work was almost completely ignored by his contemporaries. Thirty years later (1965), Bullard, Everett and Smith published in turn a similar but more sophisticated fit; they did not acknowledge Choubert's initial work. Bullard's fit was met with immediate and tremendous success. The present paper analyses the reasons why Boris Choubert was frustrated of his pioneering role. This lack of recognition is related to: (1) a great evolution in the geological concepts between 1935 and 1965, and (2) a poor choice of Choubert, regarding the title of his 1935 article.
Buikin, A.I., Trieloff, M., Korochantseeva, E.V., Hopp, J., Kaliwood, M., Meyer, H-P.,Altherr, R.
Distribution of mantle and atmospheric argon in mantle xenoliths from western Arabian Peninsula: constraints on timing and composition of metasomatizing agents....
Nestola, F., Korolev, N., Kopylova, M., Rotiroti, N., Pearson, D.G., Pamato, M.G., Alvaro, M., Peruzzo, L., Gurney, J.J., Moore, A.E., Davidson, J.
CaSiO3 perovskite in diamond indicates the recycling of oceanic crust into the lower mantle.
Nature, Vol. 555, March 8, pp. 237-241.
Mantle
deposit - Cullinan
Abstract: Laboratory experiments and seismology data have created a clear theoretical picture of the most abundant minerals that comprise the deeper parts of the Earth’s mantle. Discoveries of some of these minerals in ‘super-deep’ diamonds—formed between two hundred and about one thousand kilometres into the lower mantle—have confirmed part of this picture1,2,3,4,5. A notable exception is the high-pressure perovskite-structured polymorph of calcium silicate (CaSiO3). This mineral—expected to be the fourth most abundant in the Earth—has not previously been found in nature. Being the dominant host for calcium and, owing to its accommodating crystal structure, the major sink for heat-producing elements (potassium, uranium and thorium) in the transition zone and lower mantle, it is critical to establish its presence. Here we report the discovery of the perovskite-structured polymorph of CaSiO3 in a diamond from South African Cullinan kimberlite. The mineral is intergrown with about six per cent calcium titanate (CaTiO3). The titanium-rich composition of this inclusion indicates a bulk composition consistent with derivation from basaltic oceanic crust subducted to pressures equivalent to those present at the depths of the uppermost lower mantle. The relatively ‘heavy’ carbon isotopic composition of the surrounding diamond, together with the pristine high-pressure CaSiO3 structure, provides evidence for the recycling of oceanic crust and surficial carbon to lower-mantle depths.https://www.nature.com/articles/nature25972
Mineralogy and Petrology, doi.org/10.1007/s710-018-0601-z 15p.
Africa, South Africa
deposit - Cullinan
Abstract: We studied a suite of Cullinan diamonds (<0.3 ct) with mineral inclusions, which comprised 266 Type I and 75 blank Type II (<20 ppm N) diamonds, as classified by infrared spectroscopy. More than 90% (n?=?68) of Type II diamonds do not luminesce. In contrast, 51.9% (n?=?177) of Type I diamonds luminesce, with blue colors of different intensity. Carbon isotopic compositions of Type I and II diamonds are similar, with ?13CVPDB ranging from ?2.1 to ?7.7‰for Type I diamonds (n?=?25), and from ?1.3 to ?7.8- for Type II diamonds (n?=?20). The Type II diamonds are sourced from three parageneses, lithospheric lherzolitic (45%), lithospheric eclogitic (33%), and sublithospheric mafic (22%). The lherzolitic suite contains Cr-pyrope, forsterite, enstatite, clinopyroxene and Cr-spinel formed at 1090-1530 °C and P?=?4.6-7.0 GPa. Lithospheric eclogitic diamonds containing garnet, omphacite, kyanite and coesite comprise 33% of Type II diamonds. The sublithospheric mafic paragenesis is mainly represented by Cr-free majorite, various CaSiO3 phases and omphacite equilibrated at 11.6-26 GPa, in the transition zone and the lower mantle. The lherzolitic paragenesis predominates in Type II diamonds, whereas 79% Type I diamonds are sourced from eclogites. The higher incidence of sublithospheric inclusions was found in Type II diamonds, 22% against 6% in Type I diamonds. The similarity of the mineral parageneses and C isotopic compositions in the small Cullinan Type II and Type I diamonds indicate the absence of distinct mantle processes and carbon sources for formation of studied Type II diamonds. The parent rocks and the carbon sources generally vary for Type II diamonds within a kimberlite and between kimberlites.
Contributions to Mineralogy and Petrology, Vol. 175, 8, 25p. Pdf
Canada, Baffin Island
deposit - Chidliak
Abstract: The 156-138 Ma Chidliak kimberlites on the Eastern Hall peninsula (EHP) of Baffin Island entrained mantle xenoliths interpreted to have been a part of the Archean North Atlantic Craton (NAC) lithospheric mantle. We studied 19 Chidliak eclogite xenoliths that comprise 10 bimineralic, 5 rutile-bearing, 3 orthopyroxene-bearing and 1 kyanite-bearing eclogites. We report major and trace element compositions of the minerals, calculated bulk compositions, pressures and temperatures of the rock formation and model melt extraction from viable protoliths. The eclogite samples are classified into three groups of HREE-enriched, LREE-depleted and metasomatized based on their reconstructed whole-rock REE patterns. PT parameters of the eclogites were calculated by projecting garnet-clinopyroxene temperatures onto the local P-T arrays for 65 Chidliak peridotite xenoliths. All Chidliak eclogites are equilibrated in the diamond P-T field and cluster in two groups, low-temperature (n?=?5, 840-990 °C at 4.1-5.0 GPa) and high-temperature (n?=?11, T?>?1320 °C at P?>?7.0 GPa). The reconstructed Mg-rich major element bulk compositions and trace elements patterns are similar to Archean basalts from the North Atlantic and Superior cratons and the oceanic gabbros. The LREE-depleted Chidliak eclogites could be residues after 15-55% partial melting of Archean basalt at the eclogite facies of metamorphism that led to extraction of a tonalite-trondhjemite-granodiorite melt from the EHP. The HREE-depleted eclogites may have experienced a lower degree (<10%) of partial melting. Two eclogites may have formed after the gabbro protolith based on the presence of kyanite, high Sr content of garnet and positive Eu anomalies in garnet and bulk eclogite compositions. The metasomatism is reflected in higher Ce/Yb, Sr/Y, TiO2 or MgO of the eclogites. The average contents of MgO, FeO and CaO in NAC eclogites are statistically distinct from those in Slave craton eclogites with a probability of?>95%. The former are more magnesian, less ferrous and calcic, contain more magnesian and less calcic garnets, and lower proportions of group C eclogites. The contrast may relate to the stronger NAC metasomatism by silicate-carbonate melt observed in Chidliak peridotitic mantle, or to the different formation ages of the eclogites beneath the two cratons.
Minerals, Vol. 10, 9, 740 10.3390/ min10090740 24p. Pdf
Russia
deposit - Muna
Abstract: The oxidation state of the mantle plays an important role in many chemical and physical processes, including magma genesis, the speciation of volatiles, metasomatism and the evolution of the Earth’s atmosphere. We report the first data on the redox state of the subcontinental lithospheric mantle (SCLM) beneath the Komsomolskaya-Magnitnaya kimberlite pipe (KM), Upper Muna field, central Siberian craton. The oxygen fugacity of the KM peridotites ranges from ?2.6 to 0.3 logarithmic units relative to the fayalite-magnetite-quartz buffer (?logfO2 (FMQ)) at depths of 120-220 km. The enriched KM peridotites are more oxidized (?1.0-0.3 ?logfO2 (FMQ)) than the depleted ones (from ?1.4 to ?2.6 ?logfO2 (FMQ)). The oxygen fugacity of some enriched samples may reflect equilibrium with carbonate or carbonate-bearing melts at depths >170 km. A comparison of well-studied coeval Udachnaya and KM peridotites revealed similar redox conditions in the SCLM of the Siberian craton beneath these pipes. Nevertheless, Udachnaya peridotites show wider variations in oxygen fugacity (?4.95-0.23 ?logfO2 (FMQ)). This indicates the presence of more reduced mantle domains in the Udachnaya SCLM. In turn, the established difference in the redox conditions is a good explanation for the lower amounts of resorbed diamonds in the Udachnaya pipe (12%) in comparison with the KM kimberlites (33%). The obtained results advocate a lateral heterogeneity in the oxidation state of the Siberian SCLM.
Journal of Petrology, 10.1093/petrology /egab070 98p. Pdf
Africa, Angola
deposit - Catoca
Abstract: Reconstructed whole-rock and mineral major- and trace-element compositions, as well as new oxygen isotope data, for 22 mantle eclogite xenoliths from the Catoca pipe (Kasai Craton) were used to constrain their genesis and evolution. On the basis of mineralogical and major-element compositions, the Catoca eclogites can be divided into three groups: high-alumina (high-Al) (kyanite-bearing), low-magnesian (low-Mg#), and high-magnesian (high-Mg#) eclogites. The high-Al Catoca eclogites contain kyanite and corundum; high Al2O3 contents in rock-forming minerals; rare earth element (REE) patterns in garnets showing depleted LREEs, positive Eu anomalies (1.03-1.66), and near-flat HREEs; and high Sr contents in garnets and whole-rock REE compositions. All of these features point to a plagioclase-rich protolith (probably gabbro). Reconstructed whole-rock compositions (major elements, MREEs, HREEs, Li, V, Hf, Y, Zr, and Pb) and ?18O of 5.5-7.4‰ of the low-Mg# Catoca eclogites are in good agreement with the compositions of picrite basalts and average mid-ocean ridge basalt (MORB). The depleted LREEs and NMORB-normalised Nd/Yb values of 0.07-0.41 indicate that the degree of partial melting for the majority of the low-Mg# eclogites protolith was ?30%. The narrow ?18O range of 5.5-7.4‰ near the ‘gabbro-basalt’ boundary (6‰) obtained for the high-Al and low-Mg# Catoca eclogites reflects the influence of subduction-related processes. This case shows that mantle eclogites represented by two different lithologies and originating from different protoliths — plagioclase-rich precursor, presumably gabbro (for high-Al eclogites), and basalt (low-Mg# eclogites) — can provide similar and overlapping ?18O signatures on account of the influence of subduction-related processes. Chemical compositions of the high-Mg# eclogites indicate a complicated petrogenesis, and textural signatures reveal recrystallisation. The presence of Nb-rich rutile (8-12 wt% of Nb2O5) enriched with HFSE (Zr/Hf of 72.6-75.6) and multiple trace-element signatures (including reconstructed whole-rock NMORB-normalised Ce/Yb of 3.9-10.6 and Sr/Y of 5.8-9.6, MgO contents of 15.7-17.9 wt%, and high Ba and Sr) provide strong evidence for deep metasomatic alteration. High Cr contents in clinopyroxene (800-3740 ppm), garnet (430-1400 ppm), and accessory rutile (700-2530 ppm), together with extremely low Li contents of 1.0-2.4 ppm in clinopyroxene, may indicate hybridisation of the eclogites with peridotite. Comparison of the chemical compositions (major and trace elements) of (1) unaltered fresh cores of coarse-grained garnets from the low-Mg# eclogites, (2) secondary garnet rims (ubiquitous in the low-Mg# eclogites), (3) proto-cores in the coarse-grained garnet (high-Mg# eclogites), and (4) homogeneous recrystallised fine-grained garnets (high-Mg# eclogites) suggests that the high-Mg# eclogites formed through recrystallisation of low-Mg# eclogite in the presence of an external fluid in the mantle. Four of the five high-Mg# samples show that mantle metasomatism inside the Kasai craton mantle beneath the Catoca pipe occurred at a depth range of 145-160 km (4.5-4.8 GPa).
Abstract: Reconstructed whole-rock (RWR) and mineral major- and trace-element compositions, as well as new oxygen isotope data, for 22 mantle eclogite xenoliths from the Catoca pipe (Kasai Craton) were used to constrain their genesis and evolution. On the basis of mineralogical and major-element compositions, the Catoca eclogites can be divided into three groups: high-alumina (high-Al) (kyanite-bearing), low-magnesian (low-Mg#), and high-magnesian (high-Mg#) eclogites. The high-Al Catoca eclogites contain kyanite and corundum; high Al2O3 contents in rock-forming minerals; rare earth element (REE) patterns in garnets showing depleted LREEs, positive Eu anomalies (1.03-1.66), and near-flat HREEs; and high Sr contents in garnets and whole-rock REE compositions. All of these features point to a plagioclase-rich protolith (probably gabbro). RWR compositions (major elements, MREEs, HREEs, Li, V, Hf, Y, Zr, and Pb) and ?18O of 5.5-7.4‰ of the low-Mg# Catoca eclogites are in good agreement with the compositions of picrite basalts and average mid-ocean ridge basalt (MORB). The depleted LREEs and NMORB-normalised Nd/Yb values of 0.07-0.41 indicate that the degree of partial melting for the majority of the low-Mg# eclogites protolith was ?30%. The narrow ?18O range of 5.5-7.4‰ near the ‘gabbro-basalt’ boundary (6‰) obtained for the high-Al and low-Mg# Catoca eclogites reflects the influence of subduction-related processes. This case shows that mantle eclogites represented by two different lithologies and originating from different protoliths—plagioclase-rich precursor, presumably gabbro (for high-Al eclogites), and basalt (low-Mg# eclogites)—can provide similar and overlapping ?18O signatures on account of the influence of subduction-related processes. Chemical compositions of the high-Mg# eclogites indicate a complicated petrogenesis, and textural signatures reveal recrystallisation. The presence of Nb-rich rutile (8-12 wt% of Nb2O5) enriched with high field strength elements (HFSE) (Zr/Hf of 72.6-75.6) and multiple trace-element signatures (including RWR, NMORB-normalised Ce/Yb of 3.9-10.6 and Sr/Y of 5.8-9.6, MgO contents of 15.7-17.9 wt%, and high Ba and Sr) provide strong evidence for deep metasomatic alteration. High Cr contents in clinopyroxene (800-3740 ppm), garnet (430-1400 ppm), and accessory rutile (700-2530 ppm), together with extremely low Li contents of 1.0-2.4 ppm in clinopyroxene, may indicate hybridisation of the eclogites with peridotite. Comparison of the chemical compositions (major and trace elements) of (1) unaltered fresh cores of coarse-grained garnets from the low-Mg# eclogites, (2) secondary garnet rims (ubiquitous in the low-Mg# eclogites), (3) proto-cores in the coarse-grained garnet (high-Mg# eclogites), and (4) homogeneous recrystallised fine-grained garnets (high-Mg# eclogites) suggests that the high-Mg# eclogites formed through recrystallisation of low-Mg# eclogite in the presence of an external fluid in the mantle. Four of the five high-Mg# samples show that mantle metasomatism inside the Kasai craton mantle beneath the Catoca pipe occurred at a depth range of 145-160 km (4.5-4.8 GPa).
Russian Geology and Geophysics, Vol. 58, pp. 1305-1316.
Africa, Angola
eclogites
Abstract: We studied the Sm-Nd, Rb-Sr, and Re-Os isotope compositions of mantle xenoliths (eclogites and peridotites) from diamondiferous kimberlites of the Catoca cluster of the Kasai Craton. In the eclogites, the primary strontium isotope composition 87Sr/86Sr varies from 0.7056 to 0.7071, and the neodymium isotope composition eNd, from 1.8 to 2.6. The 187Re/188Os and 187Os/188Os ratios range from 135 to 80 and from 1.3110 to 1.9709, respectively, which indicates a significant portion of radiogenic Os: yOs = 129-147. These isotope values exceed the values assumed for model reservoirs (primitive upper mantle (PUM) and bulk silicate Earth (BSE)) and those of chondrites. The isotope composition of the studied systems indicates the formation of eclogites from a rhenium-enriched source, namely, the subducted oceanic crust transformed as a result of metasomatism and/or melting under upper-mantle conditions.
Abstract: The mantle beneath the Cullinan kimberlite (formerly known as "Premier") is a unique occurrence of diamondiferous cratonic mantle where diamonds were generated contemporaneously and shortly following a mantle upwelling that led to the formation of a Large Igneous Province that produced the world's largest igneous intrusion - the 2056?Ma Bushveld Igneous Complex (BIC). We studied 332 diamond inclusions from 202 Cullinan diamonds to investigate mantle thermal effects imposed by the formation of the BIC. The overwhelming majority of diamonds come from three parageneses: (1) lithospheric eclogitic (69%), (2) lithospheric peridotitic (21%), and (3) sublithospheric mafic (9%). The lithospheric eclogitic paragenesis is represented by clinopyroxene, garnet, coesite and kyanite. Main minerals of the lithospheric peridotitic paragenesis are forsterite, enstatite, Cr-pyrope, Cr-augite and spinel; the sublithospheric mafic association includes majorite, CaSiO3 phases and omphacite. Diamond formation conditions were calculated using an Al-in-olivine thermometer, a garnet-clinopyroxene thermometer, as well as majorite and Raman barometers. The Cullinan diamonds may be unique on the global stage in recording a cold geotherm of 40?mW/m2 in cratonic lithosphere that was in contact with underlying convecting mantle at temperatures of 1450-1550?°C. The studied Cullinan diamonds contain a high proportion of inclusions equilibrated at temperatures exceeding the ambient 1327?°C adiabat, i.e. 54% of eclogitic diamonds and 41% of peridotitic diamonds. By contrast, ? 1% of peridotitic diamond inclusions globally yield equally high temperatures. We propose that the Cullinan diamond inclusions recorded transient, slow-dissipating thermal perturbations associated with the plume-related formation of the ~2?Ga Bushveld igneous province. The presence of inclusions in diamond from the mantle transition zone at 300-650?km supports this view. Cullinan xenoliths indicative of the thermal state of the cratonic lithosphere at ~1.2?Ga are equilibrated at the relatively low temperatures, not exceeding adiabatic. The ability of diamonds to record super-adiabatic temperatures may relate to their entrainment from the deeper, hotter parts of the upper mantle un-sampled by the kimberlite in the form of xenoliths or their equilibration in a younger lithosphere after a decay of the thermal disturbance.
Abstract: Very few zircon-bearing, kimberlite-hosted mantle eclogite xenoliths have been identified to date; however, the zircon they contain is crucial for our understanding of subcratonic lithospheric mantle evolution and eclogite genesis. In this study, we constrain the characteristics of zircon from mantle eclogite xenoliths based on existing mineralogical and geochemical data from zircons from different geological settings, and on the inferred origin of mantle eclogites. Given the likely origin and subsequent evolution of mantle eclogites, we infer that the xenoliths can contain zircons with magmatic, metamorphic and xenogenic (i.e. kimberlitic zircon) origins. Magmatic zircon can be inherited from low-pressure mafic oceanic crust precursors, or might form during direct crystallization of eclogites from primary mantle-derived melts at mantle pressures. Metamorphic zircon within mantle eclogites has a number of possible origins, ranging from low-pressure hydrothermal alteration of oceanic crustal protoliths to metasomatism related to kimberlite magmatism. This study outlines a possible approach for the identification of inherited magmatic zircon within subduction-related mantle eclogites as well as xenogenic kimberlitic zircon within all types of mantle eclogites. We demonstrate this approach using zircon grains from kimberlite-hosted eclogite xenoliths from the Kasai Craton, which reveals that most, if not all, of these zircons were most likely incorporated as a result of laboratory-based contamination.
Abstract: Single crystal CVD diamond has been grown on (100)-oriented CVD diamond seed in six layers to a total thickness of 4.3 mm, each layer being grown in gas with increasing concentration of nitrogen. The nitrogen doping efficiency, distribution of color and internal stress have been studied by SIMS, optical absorption, Raman spectroscopy and birefringence imaging. It is shown that nitrogen doping is very non-uniform. This non-uniformity is explained by the terraced growth of CVD diamond. The color of the nitrogen-doped diamond is grayish-brown with color intensity gradually increasing with nitrogen concentration. The absorption spectra are analyzed in terms of two continua representing brown and gray color components. The brown absorption continuum exponentially rises towards short wavelength. Its intensity correlates with the concentration of nitrogen C-defects. Small vacancy clusters are discussed as the defects responsible for the brown absorption continuum. The gray absorption continuum has weak and almost linear spectral dependence through the near infrared and visible spectral range. It is ascribed to carbon nanoclusters which may form in plasma and get trapped into growing diamond. It is suggested that Mie light scattering on the carbon nanoclusters substantially contributes to the gray absorption continuum and determines its weak spectral dependence. A Raman line at a wavenumber of 1550 cm?1 is described as a characteristic feature of the carbon nanoclusters. The striation pattern of brown/gray color follows the pattern of anomalous birefringence suggesting that the vacancy clusters and carbon inclusions are the main cause of internal stress in CVD diamond. A conclusion is made that high perfection of seed surface at microscale is not a required condition for growth of low-stress, low-inclusion single crystal CVD diamond. Crystallographic order at macroscale is more important requirement for the seed surface.
Diamond & Related Materials, Vol. 113, 108255, 7p. Pdf
Global
luminescence
Abstract: Detailed study of the luminescence of multiple brown CVD diamonds was performed. It has been found that the well-known optical center with zero-phonon line at 468 nm is a characteristic of brown color. It has been found that the defects responsible for 468 nm center are located within brown striations suggesting close relation of the 468 nm center and the vacancy clusters. Simultaneous reduction of the intensity of 468 nm center and brown color during annealing support the assumption of their close relation. Identical spectroscopic parameters of the 468 nm center and the radiation center with ZPL at 492 nm suggest that the former relates to an intrinsic defect probably containing vacancies. The distribution of intensity of the 468 nm center in some brown diamonds follows the distribution of the NV? center while being opposite to that of the NV0 center and the dislocation-related A-band. This observation suggests the negative charge state of the 468 nm center. Due to its high luminescence efficiency, the 468 nm center can be used as a highly sensitive indicator of the traces of vacancy clusters. We found that the 468 nm center is detected practically in every as-grown CVD diamond including colorless CVD diamonds of high structural perfection and high purity.
Diamond & Related Materials, doi.1016/j.diamond.2018.11.018 30p.
Russia
synthetics
Abstract: Defect transformations in type Ib synthetic diamond annealed at a temperature of 1870?°C under stabilizing pressure (HPHT annealing) and in hydrogen atmosphere at normal pressure (LPHT annealing) are compared. Spectroscopic data obtained on the samples before and after annealing prove that the processes of nitrogen aggregation and formation of nitrogen?nickel complexes are similar in both cases. Essential differences between HPHT and LPHT annealing are stronger graphitization at macroscopic imperfections and enhanced lattice distortions around point defects in the latter case. The lattice distortion around point defects is revealed as a considerable broadening of zero-phonon lines of “soft” (vacancy-related) optical centers. It was found that LPHT annealing may enhance overall intensity of luminescence of HPHT-grown synthetic diamonds.
Korikovsky, S., Kotov, A., Salnikova, E., Aranovich, L., Korpechkov, D., Yakovleva, S., Tolmacheva, E., Anisimova, I.
The age of the protolith of metamorphic rocks in the southeastern Lapland granulite belt, southern Kola Peninsula: correlation with the Belomorian mobile belt in the context of the problem of Archean eclogites.
Xenolith of diamond bearing coesite eclogite from the Udachnaya kimberlite pipe, Yakutia.
V.S. Sobolev Institute of Geology and Mineralogy Siberian Branch Russian Academy of Sciences International Symposium Advances in high pressure research: breaking scales and horizons ( Courtesy of N. Poikilenko), Held Sept. 22-26, 2p. Abstract
Mikhno, A., Shcheptova, O., Mikhailenko, D., Korsakov, A.
Sulfides in ultrahigh pressure rocks of the Kokchetav Massif.
V.S. Sobolev Institute of Geology and Mineralogy Siberian Branch Russian Academy of Sciences International Symposium Advances in high pressure research: breaking scales and horizons ( Courtesy of N. Poikilenko), Held Sept. 22-26, 2p. Abstract
Abstract: Kimberlites of the Udachnaya-East pipe (Siberia) include a uniquely dry and serpentine-free rock type with anomalously high contents of chlorine (Cl ? 6.1 wt%), alkalies (Na2O + K2O ? 10 wt%) and sulfur (S ? 0.50 wt%), referred to as a “salty” kimberlite. The straightforward interpretation is that the Na-, K-, Cl- and S-rich components originate directly from a carbonate-chloride kimberlitic magma that is anhydrous and alkali-rich. However, because brines and evaporites are present on the Siberian craton, previous studies proposed that the kimberlitic magma was contaminated by the assimilation of salt-rich crustal rocks. To clarify the origin of high Cl, alkalies and S in this unusual kimberlite, here we determine its sulfur speciation and isotopic composition and compare it to that of non-salty kimberlites and kimberlitic breccia from the same pipe, as well as potential contamination sources (hydrothermal sulfides and sulfates, country-rock sediment and brine collected in the area). The average ?34S of sulfides is ? 1.4 ± 2.2‰ in the salty kimberlite, 2.1 ± 2.7‰ in the non-salty kimberlites and 14.2 ± 5.8‰ in the breccia. The average ?34S of sulfates in the salty kimberlites is 11.1 ± 1.8‰ and 27.3 ± 1.6‰ in the breccia. In contrast, the ?34S of potential contaminants range from 20 to 42‰ for hydrothermal sulfides, from 16 to 34‰ for hydrothermal sulfates, 34‰ for a country-rock sediment (Chukuck suite) and the regional brine aquifer. Our isotope analyses show that (1) in the salty kimberlites, neither sulfates nor sulfides can be simply explained by brine infiltration, hydrothermal alteration or the assimilation of known salt-rich country rocks and instead, we propose that they are late magmatic phases; (2) in the non-salty kimberlite and breccia, brine infiltration lead to sulfate reduction and the formation of secondary sulfides – this explains the removal of salts, alkali-carbonates and sulfates, as well as the minor olivine serpentinization; (3) hydrothermal sulfur was added to the kimberlitic breccia, but not to the massive kimberlites. In situ measurements of sulfides confirm this scenario, clearly showing the addition of two sulfide populations in the breccia (pyrite-pyrrhotites with average ?34S of 7.9 ± 3.4‰ and chalcopyrites with average ?34S of 38.0 ± 0.4‰) whereas the salty and non-salty kimberlites preserve a unique population of djerfisherites (Cl- and K-rich sulfides) with ?34S values within the mantle range. This study provides the first direct evidence of alkaline igneous rocks in which magmatic sulfate is more abundant than sulfide. Although sulfates have been rarely reported in mantle materials, sulfate-rich melts may be more common in the mantle than previously thought and could balance the sulfur isotope budget of Earth's mantle.
Bulletin de la Societe Geologique de France *eng, Vol. 188, 1-2, 8p.
Russia, Siberia
deposit - Udachnaya-East
Abstract: The Udachnaya-East pipe in Yakutia in Siberia hosts a unique dry (serpentine-free) body of hypabyssal kimberlite (<0.64wt% H2O), associated with a less dry type of kimberlite and a serpentinized kimberlitic breccia. The dry kimberlite is anomalously rich in salts (Na2O and Cl both up to 6wt%) whereas the slightly less dry and the breccia kimberlite are salt free. Yet the Udachnaya kimberlite is a group-I kimberlite, as is the archetypical kimberlite from Kimberley, South Africa. Samples were studied from the three different types of kimberlite (dry-salty, n=8, non-salty, n=5 and breccia, n=3) regarding their mineralogy, geochemistry, and more specifically their sulfur content. Our results show the salty kimberlite is unprecedentedly rich in sulfur (0.13-0.57wt%) compared to the non-salty kimberlite (0.04-0.12wt%) and the breccia (0.29-0.33wt%). In the salty kimberlite, most of the sulfur is present as sulfates (up to 97% of Stotal) and is disseminated throughout the groundmass in close association with Na-K-bearing carbonates. Sulfates occur within the crystal structure of these Na-K-bearing carbonates as the replacement of (CO3) by (SO3) groups, or as Na- and K-rich sulfates (e.g. aphtitalite, (K,Na)3Na(SO4)2). The associated sulfides are djerfisherite; also Na- and K-rich species. The close association of sulfates and carbonates in these S-rich alkaline rocks suggests that the sulfates crystallized from a mantle-derived magma, a case that has strong implication for the oxygen fugacity of kimberlite magmatism and more generally for the global S budget of the mantle.
Bulletin de la Societe Geologique de France *eng, Vol. 188, 1-2, 14p.
Russia, Siberia
deposit - Udachnaya
Abstract: Xenoliths brought up by kimberlite magmas are rare samples of otherwise inaccessible lithospheric mantle. Eclogite xenoliths are found in most cratons and commonly show a range of mineral and chemical compositions that can be used to better understand craton formation. This study focuses on five new kyanite-bearing eclogites from the Udachnaya kimberlite pipe (367±5 Ma). They are fine-to coarse-grained and consist mainly of “cloudy” clinopyroxene (cpx) and garnet (grt). The clinopyroxene is Al,Na-rich omphacite while the garnet is Ca-rich, by contrast to typical bi-mineral (cpx+grt) eclogites that contain Fe- and Mg-rich garnets. The Udachnaya kyanite eclogites are similar in modal and major element composition to those from other cratons (Dharwar, Kaapvaal, Slave, West African). The kyanite eclogites have lower REE concentrations than bi-mineral eclogites and typically contain omphacites with positive Eu and Sr anomalies, i.e. a “ghost plagioclase signature”. Because such a signature can only be preserved in non-metasomatised samples, we infer that they were present in the protoliths of the eclogites. It follows that subducted oceanic crust is present at the base of the Siberian craton. Similar compositions and textures are also seen in kyanite eclogites from other cratons, which we view as evidence for an Archean, subduction-like formation mechanism related to craton accretion. Thus, contrary to previous work that classifies all kyanite eclogites as type I (IK), metasomatized by carbonatite/kimberlitic fluids, we argue that some of them, both from this work and those from other cratons, belong to the non-metasomatized type II (IIB). The pristine type IIB is the nearest in composition to protoliths of mantle eclogites because it contains no metasomatic enrichments.
Alvaro, M., Mazzucchelli, M.L., Angel, R.J., Murri, M., Campmenosi, N., Scambelluri, M., Nestola, F., Korsakov, A., Tomilenko, A.A., Marone, F., Morana, M.
Abstract: Metamorphic rocks are the records of plate tectonic processes whose reconstruction relies on correct estimates of the pressures and temperatures (P-T) experienced by these rocks through time. Unlike chemical geothermobarometry, elastic geobarometry does not rely on chemical equilibrium between minerals, so it has the potential to provide information on overstepping of reaction boundaries and to identify other examples of non-equilibrium behavior in rocks. Here we introduce a method that exploits the anisotropy in elastic properties of minerals to determine the unique P and T of entrapment from a single inclusion in a mineral host. We apply it to preserved quartz inclusions in garnet from eclogite xenoliths hosted in Yakutian kimberlites (Russia). Our results demonstrate that quartz trapped in garnet can be preserved when the rock reaches the stability field of coesite (the high-pressure and high-temperature polymorph of quartz) at 3 GPa and 850 °C. This supports a metamorphic origin for these xenoliths and sheds light on the mechanisms of craton accretion from a subducted crustal protolith. Furthermore, we show that interpreting P and T conditions reached by a rock from the simple phase identification of key inclusion minerals can be misleading.
Abstract: A coesite-bearing diamondiferous eclogite from the Udachnaya kimberlite (Daldyn field, Siberian craton) has been studied to trace its complex evolution recorded in rock-forming and minor mineral constituents. The eclogite sample is composed of rock-forming omphacite (60 vol%), garnet (35 vol%) and quartz/coesite (5 vol%) and contains intergranular euhedral zoned olivine crystals, up to 200 µm long, coexisting with phlogopite, orthopyroxene, clinopyroxene (secondary), K-feldspar, plagioclase, spinel, sodalite and djerfisherite. Garnet grains are zoned, with a relatively homogeneous core and a more magnesian overgrowth rim. The rim zones further differ from the core in having higher Zr/Y (6 times that in the cores), ascribed to interaction with, or precipitation from, a kimberlite-related melt. Judging by pressure-temperature estimates (~1200 °C; 6.2 GPa), the xenolith originated at depths of ~180-200 km at the base of the continental lithosphere. The spatial coexistence of olivine, orthopyroxene and coesite/quartz with K-Na-Cl minerals in the xenolith indicates that eclogite reacted with a deep-seated kimberlite melt. However, Fe-rich olivine, orthopyroxene and low-pressure minerals (sodalite and djerfisherite) likely result from metasomatic reaction at shallower depths during transport of the eclogite by the erupting kimberlite melt. Our results demonstrate that a mixed eclogitic-peridotitic paragenesis, reported previously from inclusions in diamond, can form by interaction of eclogite and a kimberlite-related melt.
Perraki, M., Korsakov, A.V., Smith, D.C., Mposkos, E.
Raman spectroscopic and microscopic criteria for the distinction of microdiamonds in ultrahigh-pressure metamorphic rocks from diamonds in sample preparation materials.
Prograde zonation in ultrapotassic clinopyroxene from ultrahigh pressure garnet clinopyroxene rocks from the Kumdy-Kol mine ( Kokchetav Massif, Kazakhstan).
Doklady Earth Sciences, Vol. 447, 2, pp. 1333-1337.
Abstract: Eclogite mantle xenoliths from the central part of Siberian craton (Udachnaya and Zarnitsa kimberlite pipes) as well as from the northeastern edge of the craton (Obnazhennaya kimberlite) were studied in detail. Garnet and clinopyroxene show evident exsolution textures. Garnet comprises rutile, ilmenite, apatite, and quartz/coesite oriented inclusions. Clinopyroxene contains rutile (± ilmenite) and apatite precipitates. Granular inclusions of quartz in kyanite and garnet usually retain features of their high-pressure origin. According to thermobarometric calculations, studied eclogitic suite was equilibrated within lithospheric mantle at 3.2–4.9 GPa and 813–1080 °C. The precursor composition of garnets from Udachnaya and Zarnitsa eclogites suggests their stability at depths 210–260 km. Apatite precipitation in clinopyroxenes of Udachnaya and Zarnitsa allows us to declare that original pyroxenes could have been indicative of their high P–T stability. Raman spectroscopic study of quartz and coesite precipitates in garnet porphyroblasts confirms our hypothesis on the origin of the exsolution textures during pressure-temperature decrease. With respect to mineralogical data, we suppose the rocks to be subjected to stepwise decompression and cooling within mantle reservoir.
Abstract: The Barchi-Kol terrain is a classic locality of ultrahigh-pressure (UHP) metamorphism within the Kokchetav metamorphic belt. We provide a detailed and systematic characterization of four metasedimentary samples using dominant mineral assemblages, mineral inclusions in zircon and monazite, garnet zonation with respect to major and trace elements, and Zr-in-rutile and Ti-in-zircon temperatures. A typical diamond-bearing gneiss records peak conditions of 49 ± 4 kbar and 950-1000 °C. Near isothermal decompression of this rock resulted in the breakdown of phengite associated with a pervasive recrystallization of the rock. The same terrain also contains mica schists that experienced peak conditions close to those of the diamond-bearing rocks, but they were exhumed along a cooler path where phengite remained stable. In these rocks, major and trace element zoning in garnet has been completely equilibrated. A layered gneiss was metamorphosed at UHP conditions in the coesite field, but did not reach diamond-facies conditions (peak conditions: 30 kbar and 800-900 °C). In this sample, garnet records retrograde zonation in major elements and also retains prograde zoning in trace elements. A garnet-kyanite-micaschist that reached significantly lower pressures (24 ± 2 kbar, 710 ± 20 °C) contains garnet with major and trace element zoning. The diverse garnet zoning in samples that experienced different metamorphic conditions allows to establish that diffusional equilibration of rare earth element in garnet likely occurs at ~900-950 °C. Different metamorphic conditions in the four investigated samples are also documented in zircon trace element zonation and mineral inclusions in zircon and monazite. -Pb geochronology of metamorphic zircon and monazite domains demonstrates that prograde (528-521 Ma), peak (528-522 Ma), and peak to retrograde metamorphism (503-532 Ma) occurred over a relatively short time interval that is indistinguishable from metamorphism of other UHP rocks within the Kokchetav metamorphic belt. Therefore, the assembly of rocks with contrasting P-T trajectories must have occurred in a single subduction-exhumation cycle, providing a snapshot of the thermal structure of a subducted continental margin prior to collision. The rocks were initially buried along a low geothermal gradient. At 20-25 kbar they underwent near isobaric heating of 200 °C, which was followed by continued burial along a low geothermal gradient. Such a step-wise geotherm is in good agreement with predictions from subduction zone thermal models.
Abstract: Tychite Na6Mg2(CO3)4(SO3) is a rare natural Na and Mg sulfatocarbonate. It is found only as minor mineral in deposits of saline lakes in the United States, Canada, Uganda, and China. In these continental evaporites tychite has sedimentary genesis. In this study, we report the first occurrence of tychite as a crystal phase in the melt inclusions in olivine from mantle xenoliths of the Udachnaya-East kimberlite pipe. This find provides an evidence for the probability of tychite crystallization from melts; i.e., this rare sulfatocarbonate may have a magmatic origin as well.
Abstract: A xenolith of eclogite from the kimberlite pipe Udachnaya-East, Yakutia Grt+Cpx+Ky + S + Coe/Qtz + Dia + Gr has been studied. Graphite inclusions in diamond have been studied in detail by Confocal Raman (CR) mapping. The graphite inclusion in diamond has a highly ordered structure and is characterized by a substantial shift in the band (about 1580 cm-1) by 7 cm-1, indicating a significant residual strain in the inclusion. According to the results of FTIR spectroscopic studies of diamond crystals, a high degree of nitrogen aggregation has been detected: it is present mainly in form A, which means an "ancient" age of the diamonds. In the xenolith studied, the diamond formation occurred about 1 Byr, long before their transport by the kimberlite melt, and the conditions of the final equilibrium were temperatures of 1020 ± 40°C at 4.7 GPa. Thus, these graphite inclusions found in a diamond are the first evidence of crystallization of metastable graphite in a diamond stability field. They were formed in rocks of the upper mantle significantly below (?20 km) the graphite-diamond equilibrium line.
Abstract: Relations of graphite and diamond have been studied in a garnet-kyanite-clinopyroxene+sulfide+coesite/quartz+diamond+graphite eclogite xenolith from the Udachnaya-East kimberlite pipe in the Yakutian diamond province. Euhedral crystals of diamond and graphite occur in the intra- and intergranular space. The equilibrium conditions of diamond formation reconstructed by geothermobarometry for the Grt-Cpx-Ky-Coe mineral assemblage are 1020 ± 40 °C and 4.7 GPa. Raman imaging of graphite enclosed in diamond shows high ordering and a 9 cm?1 shift of the ~1580 cm?1 band. This Raman shift of graphite, as well as a 5 cm?1 shift of the 1332 cm?1 band of diamond, indicate large residual stress in graphite and in diamond around the inclusion, respectively. According to FTIR spectroscopy, nitrogen in diamond is highly aggregated and exists mainly as the A centers, while no other phases occur near graphite inclusions. Therefore, diamond in the analyzed eclogite sample must be quite old: it likely had crystallized long (~1 Byr) before it became entrained with kimberlite melt. New data show that graphite can stay in the upper mantle for billions of years without converting to diamond. Crystallization of various carbon polymorphs, both in laboratory and natural systems, remains poorly constrained. Graphite present in mantle and UHP rocks may be a metastable phase crystallized in the diamond stability field. This fact should be taken into consideration when deducing petrological constrains and distinguishing diamond and graphite subfacies in upper mantle.
Abstract: Abundant multiphase solid inclusions (MSI) were found in garnet in an ultrahigh-pressure (UHP) paragneiss from the Kokchetav complex, Kazakhstan. The MSI are composed of mineral associations that include rock-forming and accessory minerals, which crystallized during exhumation. We present experimental and analytical protocols for how such inclusions can be homogenized to glass and analysed for major and trace elements. After homogenization we identified two types of glass. One type is present in garnet porphyroblasts in the melanocratic part of the sample and represents a high-pressure melt formed close to peak conditions of >45 kbar, 1000°C. These inclusions are characterized by high concentrations of light rare earth elements (LREE), Th and U. Extraction of these melts resulted in a pronounced depletion of the Kokchetav gneisses in those elements. Measured partition coefficients of large ion lithophile elements (LILE) between phengite inclusions and melt inclusions are DRb?=?1•9-2•5, DBa?=?1•1-6•9 and DCs?=?0•6-0•8, resulting in limited depletion of these elements during partial melting in the presence of phengite. The Nb concentration in melts (27?ppm) is about double that in the restite (15?ppm), indicating slightly incompatible behaviour during UHP anatexis, despite the presence of residual accessory rutile and phengite. A second type of inclusion occurs in garnet from the leucocratic part of the rock and represents a late-stage melt formed during exhumation at 650-750°C and crustal pressures. These inclusions are characterized by low LREE and Nb and high U. Zircon domains formed during high-temperature melting are characterized by high Ti content (100-300?ppm) and unfractionated Th/U (0•4-0•8), whereas the low-temperature domains display low Ti (10?ppm) and Th/U (0•08). The composition of UHP melts with moderate enrichment in LILE, no depletion in Nb and extreme enrichment in LREE and Th is remarkably different from the trace element signature of arc basalts, arguing against involvement of this type of melting in the generation of arc crust. The composition of the UHP melt inclusions is similar to that of melt inclusions from HP crustal xenoliths from Pamir and also to some shoshonites from Tibet. UHP anatexis, as observed in the Kokchetav massif, might be related to the formation of shoshonitic alkaline igneous rocks, which are common in collisional settings.
Abstract: Alkaline carbonates hexagonal zemkorite (Na,K)2Ca(CO3)2 and orthorhombic shortite Na2Ca2(CO3)3 were found among groundmass minerals in kimberlites from some localities worldwide, including the unserpentinised units of the Udachnaya-East kimberlite. However, the source of alkalis and the origin of the unusual minerals in these kimberlites remain highly debatable. It is generally considered that they have hydrothermal or metasomatic origin while sodium may come from a crustal source. Orthorhombic nyerereite (Na,K)2Ca(CO3)2 and shortite were identified as daughter phases in secondary melt inclusions (MI) in olivine from the deepest mantle xenoliths (i.e., sheared peridotites) and in olivine xenocrysts derived from disintegrated mantle rocks from the Udachnaya-East pipe by Raman spectroscopy and SEM-EDS. The melt, hosted as the inclusions in olivine, was entrapped at a mantle depth. On the basis of similar mineralogy of MI to groundmass of the unserpentinised kimberlites, we suggest relation of MI to the Udachnaya kimberlite melts. The MI solidus temperature is as high as 500 °?. Generally, MI nyerereite is considered as a magmatic mineral but experiments show it to be stable at relatively low temperatures (LT) T ? 360 °?. Thus, strictly speaking, it is a subsolidus mineral formed from high-temperature (HT) (T < 800 °?) hexagonal (Na,K)2Ca(CO3)2 carbonate. Shortite is also a subsolidus mineral, which may form by several subsolidus reactions in multicomponent systems, such as kimberlites, while breakdown of the HT hexagonal phase (Na,K)2Ca(CO3,SO4)2 into Na2Ca2(CO3)3 (shortite) and K3Na(SO4)2 (aphthitalite) is the basic mechanism. The solidus temperature for the Udachnaya-East kimberlite is about 300 °? indicating that LT orthorhombic nyerereite may crystallise directly from the melt as well. Thus, (Na,K)2Ca(CO3)2 and Na2Ca2(CO3)3 carbonates in the groundmass of the unserpentinised Udachnaya-East kimberlites are of magmatic/subsolidus origin. This scenario for the origin of Na-K-Ca and Na-Ca carbonates in the Udachnaya-East kimberlites may have implications for other kimberlites elsewhere.
Abstract: We report the concentrations ([Li]) and isotopic compositions of Li in mineral separates and bulk rocks obtained by MC-ICPMS for 14 previously studied garnet and spinel peridotite xenoliths from the Udachnaya kimberlite in the central Siberian craton as well as major and trace element compositions for a new suite of 13 deformed garnet peridotites. The deformed Udachnaya peridotites occur at > 5 GPa; they are metasomatized residues of melt extraction, which as a group experienced greater modal and chemical enrichments than coarse peridotites. We identify two sub-groups of the deformed peridotites: (a) mainly cryptically metasomatized (similar to coarse peridotites) with relatively low modal cpx (< 6%) and garnet (< 7%), low Ca and high Mg#, sinusoidal REE patterns in garnet, and chemically unequilibrated garnet and cpx; (b) modally metasomatized with more cpx and garnet, higher Ca, Fe and Ti, and equilibrated garnet and cpx. The chemical enrichments are not proportional to deformation degrees. The deformation in the lower lithosphere is caused by a combination of localized stress, heating and fluid ingress from the pathways of ascending proto-kimberlite melts, with metasomatic media evolving due to reactions with wall rocks. Mg-rich olivine in spinel and coarse garnet Udachnaya peridotites has 1.2-1.9 ppm Li and ?7Li of 1.2-5.0‰, i.e. close to olivine in equilibrated fertile to depleted off-craton mantle peridotites from literature data, whereas olivine from the deformed peridotites has higher [Li] (2.4-7.5 ppm) and a broader range of ?7Li (1.8-11.6‰), which we attribute to pre-eruption metasomatism. [Li] in opx is higher than in coexisting olivine while ?7LiOl-Opx (?7LiOl ? ?7LiOpx) ranges from ? 6.6 to 7.8‰, indicating disequilibrium inter-mineral [Li] and Li-isotope partitioning. We relate these Li systematics to interaction of lithospheric peridotites with fluids or melts that are either precursors of kimberlite magmatism or products of their fractionation and/or reaction with host mantle. The melts rich in Na and carbonates infiltrated, heated and weakened wall-rock peridotites to facilitate their deformation as well as produce high [Li] and variable, but mainly high, ?7Li in olivine. The carbonate-rich melts preferentially reacted with the opx without achieving inter-mineral equilibrium because opx is consumed by such melts, and because of small volumes and uneven distribution of the metasomatic media, as well as short time spans between the melt infiltration and the capture of the wall-rock fragments by incoming portions of ascending kimberlite magma as xenoliths. Trapped interstitial liquid solidified as cryptic components responsible for high [Li] and the lack of ?7Li balance between olivine and opx, and bulk rocks. Unaltered ?26Mg values (0.20-0.26‰) measured in several olivine separates show no effects of the metasomatism on Mg-isotopes, apparently due to high Mg in the peridotites.
Abstract: We report the concentrations ([Li]) and isotopic compositions of Li in mineral separates and bulk rocks obtained by MC-ICPMS for 14 previously studied garnet and spinel peridotite xenoliths from the Udachnaya kimberlite in the central Siberian craton as well as major and trace element compositions for a new suite of 13 deformed garnet peridotites. The deformed Udachnaya peridotites occur at > 5 GPa; they are metasomatized residues of melt extraction, which as a group experienced greater modal and chemical enrichments than coarse peridotites. We identify two sub-groups of the deformed peridotites: (a) mainly cryptically metasomatized (similar to coarse peridotites) with relatively low modal cpx (< 6%) and garnet (< 7%), low Ca and high Mg#, sinusoidal REE patterns in garnet, and chemically unequilibrated garnet and cpx; (b) modally metasomatized with more cpx and garnet, higher Ca, Fe and Ti, and equilibrated garnet and cpx. The chemical enrichments are not proportional to deformation degrees. The deformation in the lower lithosphere is caused by a combination of localized stress, heating and fluid ingress from the pathways of ascending proto-kimberlite melts, with metasomatic media evolving due to reactions with wall rocks. Mg-rich olivine in spinel and coarse garnet Udachnaya peridotites has 1.2-1.9 ppm Li and ?7Li of 1.2-5.0‰, i.e. close to olivine in equilibrated fertile to depleted off-craton mantle peridotites from literature data, whereas olivine from the deformed peridotites has higher [Li] (2.4-7.5 ppm) and a broader range of ?7Li (1.8-11.6‰), which we attribute to pre-eruption metasomatism. [Li] in opx is higher than in coexisting olivine while ?7LiOl-Opx (?7LiOl ? ?7LiOpx) ranges from ? 6.6 to 7.8‰, indicating disequilibrium inter-mineral [Li] and Li-isotope partitioning. We relate these Li systematics to interaction of lithospheric peridotites with fluids or melts that are either precursors of kimberlite magmatism or products of their fractionation and/or reaction with host mantle. The melts rich in Na and carbonates infiltrated, heated and weakened wall-rock peridotites to facilitate their deformation as well as produce high [Li] and variable, but mainly high, ?7Li in olivine. The carbonate-rich melts preferentially reacted with the opx without achieving inter-mineral equilibrium because opx is consumed by such melts, and because of small volumes and uneven distribution of the metasomatic media, as well as short time spans between the melt infiltration and the capture of the wall-rock fragments by incoming portions of ascending kimberlite magma as xenoliths. Trapped interstitial liquid solidified as cryptic components responsible for high [Li] and the lack of ?7Li balance between olivine and opx, and bulk rocks. Unaltered ?26Mg values (0.20-0.26‰) measured in several olivine separates show no effects of the metasomatism on Mg-isotopes, apparently due to high Mg in the peridotites.
Earth and Planetary Science Letters, Vol. 458, 1, pp. 149-159.
Russia
deposit - Udachnaya
Abstract: Cratons represent the oldest preserved lithospheric domains. Their lithosphere (lithospheric mantle welded to overlying Precambrian crystalline basement) is considered to be particularly robust and long-lived due to the protecting presence of buoyant and rigid “keels” made up of residual harzburgites. Although the cratons are mostly assumed to form in the Archaean, the timing of their formation remains poorly constrained. In particular, there are very few datasets describing concurrently the age of both the crustal and mantle portions of the lithosphere. In this study, we report new U-Pb ages and Hf isotope compositions for zircons in crustal xenoliths from the Udachnaya kimberlite in the central Siberian craton; this dataset includes samples from both the upper and lower portions of the crust. The zircon ages agree well with model melt-extraction Re-Os ages on refractory peridotite xenoliths from the same pipe; taken together they allow an integrated view of lithosphere formation. Our data reveal that the present day upper crust is Archaean, whereas both the lower crust and the lithospheric mantle yield Paleoproterozoic ages. We infer that the deep lithosphere beneath the Siberian craton was not formed in a single Archaean event, but grew in at least two distinct events, one in the late Archaean and the other in the Paleoproterozoic. Importantly, a complete or large-scale delamination and rejuvenation of the Archaean lower lithosphere (lower crust and lithospheric mantle) took place in the Paleoproterozoic. This further demonstrates that craton formation can be a protracted, multi-stage process, and that the present day crust and mantle may not represent complementary reservoirs formed through the same tectono-magmatic event. Further, deep cratonic lithosphere may be less robust and long living than often assumed, with rejuvenation and replacement events throughout its history.
Abstract: Identification of the primary compositions of mantle-derived melts is crucial for understanding mantle compositions and physical conditions of mantle melting. However, these melts rarely reach the Earth's surface unmodified because of contamination, crystal fractionation and degassing, processes that occur almost ubiquitously after melt generation. Here we report snapshots of the melts preserved in sheared peridotite xenoliths from the Udachnaya-East kimberlite pipe, in the central part of the Siberian craton. These xenoliths are among the deepest mantle samples and were delivered by kimberlite magma from 180-230?km depth interval, i.e. from the base of the cratonic lithosphere. The olivine grains of the sheared peridotites contain secondary inclusions of the crystallized melt with bulk molar (Na?+?K)/Ca?~?3.4. Various Na-K-Ca-, Na-Ca-, Na-Mg-, Ca-Mg- and Ca-carbonates, Na-Mg-carbonates with additional anions, alkali sulphates and halides are predominant among the daughter minerals in secondary melt inclusions, whereas silicates, oxides, sulphides and phosphates are subordinate. These inclusions can be considered as Cl-S-bearing alkali-carbonate melts. The presence of aragonite, a high-pressure polymorph of CaCO3, among the daughter minerals suggests a mantle origin for these melt inclusions. The secondary melt inclusions in olivine from the sheared peridotite xenoliths and the melt inclusions in phenocrystic olivines from the host kimberlites demonstrate similarities, in daughter minerals assemblages and trace-element compositions. Moreover, alkali-rich minerals (carbonates, halides, sulphates and sulphides) identified in the studied melt inclusions are also present in the groundmass of the host kimberlites. These data suggests a genetic link between melt enclosed in olivine from the sheared peridotites and melt parental to the Udachnaya-East kimberlites. We suggest that the melt inclusions in olivine from mantle xenoliths may represent near primary, kimberlite melts. These results are new evidence in support of the alkali?carbonate composition of kimberlite melts in their source regions, prior to the kimberlite emplacement into the crust, and are in stark contrast to the generally accepted ultramafic silicate nature of parental kimberlite liquids.
Abstract: Elastic geobarometry for host-inclusion systems can provide new constraints to assess the pressure and temperature conditions attained during metamorphism. Current experimental approaches and theory are developed only for crystals immersed in a hydrostatic stress field, whereas inclusions experience deviatoric stress. We have developed a method to determine the strains in quartz inclusions from Raman spectroscopy using the concept of the phonon-mode Grüneisen tensor. We used ab initio Hartree-Fock/Density Functional Theory to calculate the wavenumbers of the Raman-active modes as a function of different strain conditions. Least-squares fits of the phonon-wavenumber shifts against strains have been used to obtain the components of the mode Grüneisen tensor of quartz (??m1 and ?m3?) that can be used to calculate the strains in inclusions directly from the measured Raman shifts. The concept is demonstrated with the example of a natural quartz inclusion in eclogitic garnet from Mir kimberlite and has been validated against direct X-ray diffraction measurement of the strains in the same inclusion.
Abstract: Identification of the primary compositions of mantle-derived melts is crucial for understanding mantle compositions and physical conditions of mantle melting. However, these melts rarely reach the Earth's surface unmodified because of contamination, crystal fractionation and degassing, processes that occur almost ubiquitously after melt generation. Here we report snapshots of the melts preserved in sheared peridotite xenoliths from the Udachnaya-East kimberlite pipe, in the central part of the Siberian craton. These xenoliths are among the deepest mantle samples and were delivered by kimberlite magma from 180-230?km depth interval, i.e. from the base of the cratonic lithosphere. The olivine grains of the sheared peridotites contain secondary inclusions of the crystallized melt with bulk molar (Na?+?K)/Ca?~?3.4. Various Na-K-Ca-, Na-Ca-, Na-Mg-, Ca-Mg- and Ca-carbonates, Na-Mg-carbonates with additional anions, alkali sulphates and halides are predominant among the daughter minerals in secondary melt inclusions, whereas silicates, oxides, sulphides and phosphates are subordinate. These inclusions can be considered as Cl-S-bearing alkali-carbonate melts. The presence of aragonite, a high-pressure polymorph of CaCO3, among the daughter minerals suggests a mantle origin for these melt inclusions. The secondary melt inclusions in olivine from the sheared peridotite xenoliths and the melt inclusions in phenocrystic olivines from the host kimberlites demonstrate similarities, in daughter minerals assemblages and trace-element compositions. Moreover, alkali-rich minerals (carbonates, halides, sulphates and sulphides) identified in the studied melt inclusions are also present in the groundmass of the host kimberlites. These data suggests a genetic link between melt enclosed in olivine from the sheared peridotites and melt parental to the Udachnaya-East kimberlites. We suggest that the melt inclusions in olivine from mantle xenoliths may represent near primary, kimberlite melts. These results are new evidence in support of the alkali?carbonate composition of kimberlite melts in their source regions, prior to the kimberlite emplacement into the crust, and are in stark contrast to the generally accepted ultramafic silicate nature of parental kimberlite liquids.
Abstract: Kyanite gneiss from the “New Barchinsky” locality (Kokchetav Massif) was studied in detail. This rock is characterized by zonal distribution of the C and SiO2 polymorphs in kyanite porphyroblasts: (1) cores with graphite and quartz inclusions; (2) clean overgrowth zone with inclusions of cuboctahedral diamond crystals. The Raman mapping of SiO2 polymorphs originally showed the presence of an association of disordered graphite + coesite “prohibited” in HT diamond-bearing rocks. Graphitization of diamond is the only likely mechanism of the disordered graphite formation in HT diamond-bearing rocks. However, the absence of disordered graphite in association with diamond in kyanite porphyroblasts from kyanite gneiss from the “New Barchinsky” locality eliminates the process of diamond graphitization at the retrograde stage. Most likely, crystallization of disordered graphite occurred at the retrograde stage from the UHP C-O-H fluid.
Abstract: Large-ion lithophile elements (LILE)-enriched chromium titanates of the magnetoplumbite (AM12O19) and crichtonite (ABC18T2O38) groups have been recognized as abundant inclusions in orthopyroxene grains in a mantle-derived xenolith from the Udachnaya-East kimberlite pipe, Daldyn field, Siberian craton. The studied xenolith consists of three parts: an orthopyroxenite, a garnet clinopyroxenite, and a garnet-orthopyroxene intermediate domain between the two. Within the host enstatite (Mg# 92.6) in the orthopyroxenitic part of the sample titanate inclusions are associated with Cr-spinel, diopside, rutile, Mg-Cr-ilmenite, and pentlandite. Crichtonite-group minerals also occur as acicular inclusions in pyrope grains of the intermediate domain adjacent to the orthopyroxenite, as well as in interstitial to enstatite oxide intergrowths together with Cr-spinel, rutile, and ilmenite. Yimengite-hawthorneite inclusions in enstatite contain (wt%) 3.72-8.04 BaO, 2.05-3.43 K2O, and 0.06-0.48 CaO. Their composition is transitional between yimengite and hawthorneite end-members with most grains exhibiting K-dominant chemistry. A distinct feature of the studied yimengitehawthorneite minerals is a high content of Al2O3 (5.74-7.69 wt%). Crichtonite-group minerals vary in compositions depending on the occurrence in the xenolith: inclusions in enstatite are moderate-high in TiO2 (62.9-67.1 wt%), moderately Cr-rich (12.6-14.0 wt% Cr2O3), Ba- or K-specific in the A site, and contain low ZrO2 (0.05-1.72 wt%), whereas inclusions in pyrope are moderate in TiO2 (61.7-63.3 wt% TiO2), relatively low in Cr (8.98-9.62 wt% Cr2O3), K-dominant in the A site, and are Zr-enriched (4.64-4.71 wt% ZrO2). Crichtonite-group minerals in polymineralic oxide intergrowths show highly diverse compositions even within individual aggregates, where they are chemically dominated by Ba, Ca, and Sr. P-T estimates indicate the orthopyroxenite to have equilibrated at ~800 °C and 35 kbar. Preferentially oriented lamellae of enstatite-hosted Cr-spinel and diopside, as well as pyrope, diopside, and Cr-spinel grains developed around enstatite crystals, are interpreted to have been exsolved from the high-T Ca-Al-Cr-enriched orthopyroxene precursor. The exotic titanate compositions and observed textural relationships between inclusions in enstatite imply that the studied orthopyroxenite has undergone metasomatic processing by a mobile percolating agent afterward; this highly evolved melt/fluid was enriched in Ba, K, HFSE, and other incompatible elements. The infiltration of the metasomatizing liquid occurred through interstices and vulnerable zones of enstatite grains and manifested in the crystallization of titanate inclusions. It is assumed that Cr-spinel lamellae served as seeds for their nucleation and growth. The prominent textural and chemical inhomogeneity of the interstitial oxide intergrowths is either a consequence of the metasomatic oxide crystallization shortly prior to the kimberlite magma eruption or arose from the intensive modification of preexisting oxide clusters by the kimberlite melt during the Udachnaya emplacement. Our new data provide implications for the metasomatic treatment of orthopyroxenites in the subcontinental lithospheric mantle from the view of exotic titanate occurrences.
Journal of Raman Spectroscopy, in press available, 19p. Pdf
Russia
deposit - Udachnaya
Abstract: The study of kimberlite rocks is important as they provide critical information regarding the composition and dynamics of the continental mantle and are the principal source of diamonds. Despite many decades of research, the original compositions of kimberlite melts, which are thought to be derived from depths > 150 km, remain highly debatable due to processes that can significantly modify their composition during ascent and emplacement. Snapshots of the kimberlite?related melts were entrapped as secondary melt inclusions hosted in olivine from sheared peridotite xenoliths from the Udachnaya?East pipe (Siberian craton). These xenoliths originated from 180? to 220?km depth and are among the deepest derived samples of mantle rocks exposed at the surface. The crystallised melt inclusions contain diverse daughter mineral assemblages (>30 mineral species), which are dominated by alkali?rich carbonates, sulfates, and chlorides. The presence of aragonite as a daughter mineral suggests a high?pressure origin for these inclusions. Raman?mapping studies of unexposed inclusions show that they are dominated by carbonates (>65 vol.%), whereas silicates are subordinate (<13 vol.%). This indicates that the parental melt for the inclusions was carbonatitic. The key chemical features of this melt are very high contents of alkalis, carbon dioxide, chlorine, and sulfur and extremely low silica and water. Alkali?carbonate melts entrapped in xenolith minerals likely represent snapshots of the primitive kimberlite melt. This composition is in contrast with the generally accepted notion that kimberlites originated as ultramafic silicate water?rich melts. Experimental studies revealed that alkali?carbonate melts are a very suitable diamond?forming media. Therefore, our findings support the idea that some diamonds and kimberlite magmatism may be genetically related.
Abstract: A find of coesite in a kyanite graphite-diamond-bearing eclogite xenolith from the Udachnaya-Vostochnaya kimberlite pipe is described in this paper. The coesite relics were found in intensely fractured garnet indicating some influence of the kimberlite melt, which is supported by the typical secondary mineral assemblage around this inclusion. These data indicate that shallower diamond-free coesite-grade rocks (2.7 GPa) underwent metamorphism distinct from diamond-bearing coesite eclogites (?4 GPa). The metasomatic alteration of rock as a result of the C-O-H fluid-rock interaction during diamond crystallization may be another possible reason for the absence of coesite in diamond-bearing xenoliths.
Abstract: More than forty mineral species of epigenetic origin have been identified in an orthopyroxenite from the Udachnaya-East kimberlite pipe, Daldyn kimberlite field, Siberian platform. Epigenetic phases occur as: (1) Mineral inclusions in the rock-forming enstatite, (2) daughter minerals within large (up to 2 mm) crystallized melt inclusions (CMI) in the rock-forming enstatite, and (3) individual grains and intergrowths in the intergranular space of the xenolith. The studied minerals include silicates (olivine, clinopyroxene, phlogopite, tetraferriphlogopite, amphibole-supergroup minerals, serpentine-group minerals, talc), oxides (several generations of ilmenite and spinel, rutile, perovskite, rare titanates of the crichtonite, magnetoplumbite and hollandite groups), carbonates (calcite, dolomite), sulfides (pentlandite, djerfisherite, pyrrhotite), sulfate (barite), phosphates (apatite and phosphate with a suggested crystal-chemical formula Na2BaMg[PO4]2), oxyhydroxide (goethite), and hydroxyhalides (kuliginite, iowaite). The examined epigenetic minerals are interpreted to have crystallized at different time spans after the formation of the host rock. The genesis of minerals is ascribed to a series of processes metasomatically superimposed onto the orthopyroxenite, i.e., deep-seated mantle metasomatism, infiltration of a kimberlite-related melt and late post-emplacement hydrothermal alterations. The reaction of orthopyroxene with the kimberlite-related melt has led to orthopyroxene dissolution and formation of the CMI, the latter being surrounded by complex reaction zones and containing zoned olivine grains with extremely high-Mg# (up to 99) cores. This report highlights the utility of minerals present in minor volume proportions in deciphering the evolution and modification of mantle fragments sampled by kimberlitic and other deep-sourced magmas. The obtained results further imply that the whole-rock geochemical analyses of mantle-derived samples should be treated with care due to possible drastic contaminations from “hiding” minor phases of epigenetic origin.
Abstract: Raman spectroscopy is widely applied in metamorphic petrology and offers many opportunities for geological and tectonic research. Minimal sample preparation preserves sample integrity and microtextural information, while use with confocal microscopes allows spatial resolution down to the micrometer level. Raman spectroscopy clearly distinguishes mineral polymorphs, providing crucial constraints on metamorphic conditions, particularly ultrahigh-pressure conditions. Raman spectroscopy can also be used to monitor the structure of carbonaceous material in metamorphic rocks. Changes in structure are temperature-sensitive, so Raman spectroscopy of carbonaceous material is widely used for thermometry. Raman spectroscopy can also detect and quantify strain in micro-inclusions, offering new barometers that can be applied to understand metamorphic and tectonic processes without any assumptions about chemical equilibrium.
Geochimica et Cosmochimica Acta, Vol. 281, pp. 67-90. pdf
Russia, Siberia
deposit - Udachnaya
Abstract: Cratonic lithospheric mantle is believed to have been formed in the Archean, but kimberlite-hosted coarse peridotites from Udachnaya in the central Siberian craton typically yield Paleoproterozoic Re-depletion Os isotope ages (TRD). By comparison, olivine megacrysts from Udachnaya, sometimes called “megacrystalline peridotites”, often yield Archean TRD ages, but the nature of these rare materials remains enigmatic. We provide whole-rock (WR) Re-Os isotope and PGE analyses for 24 olivine-rich xenoliths from Udachnaya as well as modal and petrographic data, WR and mineral major and trace element compositions. The samples were selected based on (a) high olivine abundances in hand specimens and (b) sufficient freshness and size to yield representative WR powders. They comprise medium- to coarse-grained (olivine?1?cm) dunites, a megacrystalline (olivine?>?1?cm) dunite, olivine megacrysts and low-orthopyroxene (11-21% opx) harzburgites equilibrated at 783-1154?°C and 3.9-6.5 GPa; coarse dunites have not been previously reported from Udachnaya; two xenoliths contain ilmenite. The harzburgites and dunites have similar WR variation ranges of Ca, Al, Fe, Cr and Mg# (0.917-0.934) typical of refractory cratonic peridotites, but the dunites tend to have higher MgO, NiO and Mg/Si. Mineral abundances and those of Ca and Al are not correlated with Mg#WR; they are not due to differences in melting degrees but are linked to metasomatism. Several samples with high 187Re/188Os show a positive linear correlation with 187Os/188Os with an apparent age of 0.37?Ga, same as eruption age of host kimberlite. Robust TRD ages were obtained for 16 xenoliths with low 187Re/188Os (0.02-0.13). TRD ages for low-opx harzburgites (1.9-2.1?Ga; average 2.0?±?0.1?Ga, 1 ?) are manifestly lower than for dunites and megacrysts (2.4-3.1?Ga); the latter define two subsets with average TRD of 2.6?±?0.1?Ga and 3.0?±?0.1?Ga, and TMA of 3.0?±?0.2?Ga and 3.3?±?0.1?Ga, respectively. Differences in olivine grain size (coarse vs. megacrystalline) are not related to age. The age relations suggest that the dunites and megacrysts could not be produced by re-melting of harzburgites, e.g. in arc settings, nor be melt channel materials in harzburgites. Instead, they are relict fragments of lithospheric mantle formed in the Archean (likely in two events at or after 2.6?Ga and 3.0?Ga) that were incorporated into cratonic lithosphere during the final assembly of the Siberian craton in the Paleoproterozoic. A multi-stage formation of the Siberian lithospheric mantle is consistent with crustal basement ages from U-Pb dating of zircons from crustal xenoliths at Udachnaya and detrital zircons from the northern Siberian craton (1.8-2.0, 2.4-2.8 and 3.0-3.4?Ga). The new data from the Siberian and other cratons suggest that the formation of strongly melt-depleted cratonic lithosphere (e.g. Mg# ?0.92) did not stop at the Archean-Proterozoic boundary as is commonly thought, but continued in the Paleoproterozoic. The same may be valid for the transition from the ‘Archean’ (4-2.5?Ga) to modern tectonic regimes.
Journal of Raman Spectroscopy, doi.org/10.1002/jrs.5701 19p pdf
Russia
deposit - Udachnaya-East
Abstract: The study of kimberlite rocks is important as they provide critical information regarding the composition and dynamics of the continental mantle and are the principal source of diamonds. Despite many decades of research, the original compositions of kimberlite melts, which are thought to be derived from depths > 150 km, remain highly debatable due to processes that can significantly modify their composition during ascent and emplacement. Snapshots of the kimberlite?related melts were entrapped as secondary melt inclusions hosted in olivine from sheared peridotite xenoliths from the Udachnaya?East pipe (Siberian craton). These xenoliths originated from 180? to 220?km depth and are among the deepest derived samples of mantle rocks exposed at the surface. The crystallised melt inclusions contain diverse daughter mineral assemblages (>30 mineral species), which are dominated by alkali?rich carbonates, sulfates, and chlorides. The presence of aragonite as a daughter mineral suggests a high?pressure origin for these inclusions. Raman?mapping studies of unexposed inclusions show that they are dominated by carbonates (>65 vol.%), whereas silicates are subordinate (<13 vol.%). This indicates that the parental melt for the inclusions was carbonatitic. The key chemical features of this melt are very high contents of alkalis, carbon dioxide, chlorine, and sulfur and extremely low silica and water. Alkali?carbonate melts entrapped in xenolith minerals likely represent snapshots of the primitive kimberlite melt. This composition is in contrast with the generally accepted notion that kimberlites originated as ultramafic silicate water?rich melts. Experimental studies revealed that alkali?carbonate melts are a very suitable diamond?forming media. Therefore, our findings support the idea that some diamonds and kimberlite magmatism may be genetically related.
MDPI Minerals, Vol. 10, 264, doi.10.3390/ min10030264 34p. Pdf
Russia
deposit - Udachnaya-East
Abstract: More than forty mineral species of epigenetic origin have been identified in an orthopyroxenite from the Udachnaya-East kimberlite pipe, Daldyn kimberlite field, Siberian platform. Epigenetic phases occur as: (1) Mineral inclusions in the rock-forming enstatite, (2) daughter minerals within large (up to 2 mm) crystallized melt inclusions (CMI) in the rock-forming enstatite, and (3) individual grains and intergrowths in the intergranular space of the xenolith. The studied minerals include silicates (olivine, clinopyroxene, phlogopite, tetraferriphlogopite, amphibole-supergroup minerals, serpentine-group minerals, talc), oxides (several generations of ilmenite and spinel, rutile, perovskite, rare titanates of the crichtonite, magnetoplumbite and hollandite groups), carbonates (calcite, dolomite), sulfides (pentlandite, djerfisherite, pyrrhotite), sulfate (barite), phosphates (apatite and phosphate with a suggested crystal-chemical formula Na2BaMg[PO4]2), oxyhydroxide (goethite), and hydroxyhalides (kuliginite, iowaite). The examined epigenetic minerals are interpreted to have crystallized at different time spans after the formation of the host rock. The genesis of minerals is ascribed to a series of processes metasomatically superimposed onto the orthopyroxenite, i.e., deep-seated mantle metasomatism, infiltration of a kimberlite-related melt and late post-emplacement hydrothermal alterations. The reaction of orthopyroxene with the kimberlite-related melt has led to orthopyroxene dissolution and formation of the CMI, the latter being surrounded by complex reaction zones and containing zoned olivine grains with extremely high-Mg# (up to 99) cores. This report highlights the utility of minerals present in minor volume proportions in deciphering the evolution and modification of mantle fragments sampled by kimberlitic and other deep-sourced magmas. The obtained results further imply that the whole-rock geochemical analyses of mantle-derived samples should be treated with care due to possible drastic contaminations from “hiding” minor phases of epigenetic origin.
Abstract: A series of precise nondestructive analytical methods (Raman spectroscopy, cathodoluminescence, and EBSD—electron backscatter diffraction) has been employed to investigate the internal textures of kyanite porphyroblasts from diamondiferous and diamond?free ultrahigh?pressure metamorphic rocks (Kokchetav massif, Northern Kazakhstan). Such internal kyanite characteristics as twinning, radial fibrous pattern, and spotty zoning were identified by means of Raman and cathodoluminescence imaging, whereas an intergrowth of two kyanite crystals was distinguished only by Raman imaging. The EBSD analysis recorded an ~10-25° changing of orientations along the elongation in the investigated kyanite porphyroblasts. The absence of a radial fibrous pattern and a spotty zoning on the EBSD maps indicates that these textures are not related to variations in crystallographic orientation. The absence of clear zoning patterns (cores, mantles, and rims) on the Raman, cathodoluminescence, or EBSD maps of the kyanite porphyroblasts indicates the rapid single?stage formation of these porphyroblasts near the peak metamorphic conditions and the lack of recrystallization processes. The obtained results provide important implications for deciphering of mineral internal textures, showing that the data obtained by cathodoluminescence mapping can be clearly reproduced by Raman imaging, with the latter method occasionally being even more informative. This observation is of significant importance for the study of minerals that are unexposed on a thin section surface or Fe? and Ni?rich minerals that do not show luminescence emission. The combination of the Raman spectroscopic, cathodoluminescence, and EBSD techniques may provide better spatial resolution for distinguishing different domains and textural peculiarities of mineral than the selective application of individual approaches.
Nature Communications, doi:.org/10.1038/ s41467-020-17442 -8 11p. Pdf
Africa, South Africa, Russia, Siberia
water
Abstract: Trace amounts of water dissolved in minerals affect density, viscosity and melting behaviour of the Earth’s mantle and play an important role in global tectonics, magmatism and volatile cycle. Water concentrations and the ratios of hydrogen isotopes in the mantle give insight into these processes, as well as into the origin of terrestrial water. Here we show the presence of molecular H2 in minerals (omphacites) from eclogites from the Kaapvaal and Siberian cratons. These omphacites contain both high amounts of H2 (70 to 460 wt. ppm) and OH. Furthermore, their ?D values increase with dehydration, suggesting a positive H isotope fractionation factor between minerals and H2-bearing fluid, contrary to what is expected in case of isotopic exchange between minerals and H2O-fluids. The possibility of incorporation of large quantities of H as H2 in nominally anhydrous minerals implies that the storage capacity of H in the mantle may have been underestimated, and sheds new light on H isotope variations in mantle magmas and minerals.
Contributions to Mineralogy and Petrology, Vol. 175, 107, 17p. Pdf
Russia
deposit - Udachnaya
Abstract: The formation of diamonds within eclogitic rocks has been widely linked to the fate of carbon during subduction and, therefore, referred to conditions of pressure, temperature, and oxygen fugacity (fo2). Mantle-derived eclogite xenoliths from Udachnaya kimberlite pipes represent a unique window to investigate the formation of carbon-free, graphite-diamond-bearing and diamond-bearing rocks from the Siberian craton. With this aim, we exploited oxy-thermobarometers to retrieve information on the P-T-fo2 at which mantle eclogites from the Siberian craton equilibrated along with elemental carbon. The chemical analyses of coupled garnet and omphacitic clinopyroxene were integrated with data on their iron oxidation state, determined both by conventional and synchrotron 57Fe Mössbauer spectroscopy. The calculated fo2s largely vary for each suite of eclogite samples from 0.10 to ? 2.43 log units (?FMQ) for C-free eclogites, from ? 0.01 to ? 2.91 (?FMQ) for graphite-diamond-bearing eclogites, and from ? 2.08 to ? 3.58 log units (?FMQ) for diamond-bearing eclogites. All eclogite samples mostly fall in the fo2 range typical of diamond coexisting with CO2-rich water-bearing melts and gaseous fluids, with diamondiferous eclogites being more reduced at fo2 conditions where circulating fluids can include some methane. When uncertainties on the calculated fo2 are taken into account, all samples essentially fall within the stability field of diamonds coexisting with CO2-bearing melts. Therefore, our results provide evidence of the potential role of CO2-bearing melts as growth medium on the formation of coexisting diamond and graphite in mantle eclogites during subduction of the oceanic crust.
Abstract: Mineral inclusions in cubic diamonds from garnet-clinopyroxene rock of the Kokchetav massif were studied. The coexistence of fluid and silicate inclusions in the central part of the diamond of the G0 sample was revealed by means of transmission electron microscopy. Silicate inclusions are represented by intergrowths of garnet and mica, which are spatially related with the carbonate and fluid inclusions. The first finding of silicate inclusions in the cubic diamonds from the UHP complex discovered over 50 years of their study is apparently due to a selective capture of the silicate minerals in the process of the diamond crystallization from the carbonate-bearing C-O-H fluid. The processes of diamond crystallization in the metamorphic deeply subducted rocks and upper mantle rocks, which are carried to the surface as xenoliths by kimberlite melts, have much in common.
Abstract: This study highlights the usefulness of rutile when applied for reconstruction of the metamorphic evolution of ultrahigh-pressure rocks containing diamond. Within the diamondiferous kyanite gneiss (Kokchetav massif, Northern Kazakhstan), rutile shows three distinct textural positions: (i) rounded/irregular-shaped grains in the rock matrix; (ii) monomineralic inclusions in garnet, kyanite, quartz, and zircon; and (iii) grains in polyphase inclusions within garnet and kyanite porphyroblasts. High Nb (1990-3197 ppm) and relatively low Cr (404-703 ppm) concentrations in rutile indicate its metapelitic derivation. The Zr content in rutile varies from 480 to 798 ppm and the average temperature estimates yielded by the Zr-in-rutile geothermometer for 5 GPa are 880 °C. Rutile-hosted Zn-rich (up to 1.74 wt% ZnO) staurolite is interpreted as a record of the prograde metamorphic stage formed as a result of gahnite+pyrophyllite+diaspore breakdown at 0.3-0.8 GPa, 400-450 °C. Inclusions of diamond±CO2 ± carbonate±garnet in rutile originated near the peak of metamorphism (~5 GPa and ~ 880 °C). U-Pb ID-TIMS dating of a representative rutile separate yielded a concordant age of 519 ± 1.6 Ma that is younger than the previously estimated U-Pb crystallization ages of the peak metamorphic assemblages of the Kokchetav massif (528 ± 3 Ma). The obtained age represents the timing of cooling to the closure temperature for Pb diffusion in rutile (Tc; 420-640 °C). The cooling of the rocks from the peak temperatures to Tc occurred with the rates of 27-51 °C/Ma, whereas the exhumation rates (from 880 °C and 5 GPa to 420-640 °C and 0.5-1 GPa) were 1.3-1.5 cm/year. The peak temperature estimates as well as rapid cooling and exhumation rates reported here are in agreement with published data on zircon from similar diamondiferous Kokchetav gneisses. This work demonstrates that rutile provides a beneficial tool in studies dealing with reconstruction of the metamorphic evolution of diamondiferous rocks.
Abstract: Kimberlite-borne mantle eclogites represent an important diamond source rock. Although the origin and stability of diamond, as opposed to its low-pressure polymorph graphite, have been studied for decades, their relationship in rare natural samples where both polymorphs coexist remains poorly constrained. To shed new light on this issue, seven graphite-diamond-bearing eclogites from the kimberlite pipe Udachnaya, Siberian craton were comprehensively investigated with respect to their petrography, mineral chemical composition and omphacite 87Sr/86Sr, acquired in situ by laser ablation multicollector inductively coupled plasma mass spectrometry. The calculated P-T conditions for basaltic group eclogites (Eu/Eu* < 1) correspond to a pressure range of 4•8-6•5?GPa and temperatures of 1060-1130?°C, whereas gabbroic eclogites with positive Eu- and Sr-anomalies have a smaller pressure variation (4•8-5•8?GPa), but a larger range in temperature (990-1260?°C). Reconstructed bulk compositions for gabbroic eclogites indicate an oceanic crustal origin for their protoliths, with accumulation of plagioclase and olivine ± clinopyroxene (gabbronorite or olivine gabbro). The protoliths of basaltic eclogites probably formed from the complementary residual melt. The presence of coesite and low Mg# in basaltic eclogites suggest that their light rare earth element depletion was the result of <10?% partial melting during subsequent subduction and emplacement into the cratonic lithosphere. Extremely unradiogenic 87Sr/86Sr (0•70091-0•70186 for six of seven samples) not only provides new evidence for the Archean age (2•5-2•9?Gyr) of Yakutian graphite-diamond-bearing eclogites and for formation of their protoliths in a depleted mantle source, but also suggests that they were not significantly metasomatically overprinted after their formation, despite their extended residence in the cratonic mantle lithosphere. The mineralogical and petrographic features indicate that the primary mineral association includes garnet, omphacite, ± coesite, ± kyanite, ± rutile, graphite, and diamond. Graphite occurs in the samples in the form of idiomorphic crystals (the longest dimensions being 0•4-1?mm) in garnet and kyanite and extends beyond their grain boundaries. Diamonds occur as octahedral cubic transparent, slightly colored or bright yellow crystals as large as 0•1-2?mm. Furthermore, idiomorphic and highly ordered graphite occurs as inclusions in diamond in four samples. The carbon isotope composition for diamond and graphite has a narrow range (?4 to ?6•6?‰) for both groups (gabbroic and basaltic), indicating a mantle source and limiting the role of subducted isotopically light biogenic carbon or reduction of isotopically heavy carbonate in diamond crystallization. Importantly, the presence of graphite and diamond inclusions in garnet, omphacite, and kyanite in three samples indicates a co-formation close in time to eclogitization. Combined, the petrographic and geochemical evidence suggests that both polymorphic carbon modifications can form in the diamond stability field, as also suggested by experiments and some natural examples, although the exact mechanism remains unresolved. Furthermore, this study provides natural evidence that graphite can be preserved (metastably) deep within the diamond stability field, without recrystallizing into diamond, for a long time, ?2•5?Gyr.
Abstract: Pyrope xenocrysts (N = 52) with associated inclusions of Ti- and/or Cr-rich oxide minerals from the Aldanskaya dyke and Ogonek diatreme (Chompolo field, southeastern Siberian craton) have been investigated. The majority of xenocrysts are of lherzolitic paragenesis and have concave-upwards (normal) rare earth element (REEN) patterns that increase in concentration from light REE to medium-heavy REE (Group 1). Four Ca-rich (5.7-7.4 wt.% CaO) pyropes are extremely low in Ti, Na and Y and have sinusoidal REEN spectra, thus exhibiting distinct geochemical signatures (Group 2). A peculiar xenocryst, s165, is the only sample to show harzburgitic derivation, whilst demonstrating a normal-to-weakly sinusoidal REEN pattern and the highest Zr (93 ppm) and Sc (471 ppm). Chromite-magnesiochromite, rutile, Mg-ilmenite and crichtonite-group minerals comprise a suite of oxide mineral inclusions in the pyrope xenocrysts. These minerals are characteristically enriched in Cr with 0.6-7.2 wt.% Cr2O3 in rutile, 0.7-3.6 wt.% in Mg-ilmenite and 7.1-18.0 wt.% in the crichtonite-group minerals. Complex titanates of the crichtonite group enriched in large ion lithophile elements (LILE) are high in Al2O3 (0.9-2.2 wt.%), ZrO2 (1.5-5.4 wt.%) and display a trend of compositions from the Ca-Sr-specific varieties to the Ba-dominant species (e.g. lindsleyite). In the pyrope xenocrysts the oxides coexist with silicates (clino- and orthopyroxene and olivine), hydrous silicates (talc, phlogopite and amphibole), carbonate (magnesite), sulfides (pentlandite, chalcopyrite, breakdown products of monosulfide and bornite solid solutions), apatite and graphite. P-T estimates imply the inclusion-bearing pyrope xenocrysts have been derived from low-temperature peridotite assemblages that resided at temperatures of ~600-800°C and a pressure range of ~25-35 kbar in the graphite stability field. Pyrope genesis is linked to the metasomatic enrichment of peridotite protoliths by Ca-Zr-LILE-bearing percolating fluid-melt phases containing significant volatile components. These metasomatic agents are probably volatile-rich melts or supercritical C-O-H-S fluids that were released from a Palaeo-subduction slab.
Abstract: The mineralogical and geochemical features of titanite and associated minerals in a rare sample of kyanite-coesite-rutile-bearing eclogite from the Udachnaya-East (Vostochnaya) kimberlite pipe have been studied in detail. Subidiomorphic titanite grains (100-300 ?m) were identified in the intergranular space. The composition of individual grains of titanite is characterized by a constant presence of Al2O3, F, P2O5, Zr, and Sr impurities but varies within the xenolith. Based on the absence of titanite inclusions in the rock-forming minerals and their presence in the intergranular space, titanite was formed in the studied sample at a late stage of its formation, most likely in the process of metasomatic action of the fluid/melt. Crystallization of rock-forming minerals (garnet + omphacite + kyanite) and accessory rutile occurred jointly at 3.5 ± 0.32 GPa and 920 ± 65°?. The value of Eu/Eu* = 1.06 in the reconstructed bulk composition of the rock, the high modal content of kyanite (~17 vol %), and the value of Ca# = Ca/(Ca + Mg + Fe + Mn) > 0.5 in garnet indicate a subduction nature of the studied eclogite. Most likely, the formation of titanite in the studied sample occurred as a result of the metasomatic action of a fluid/melt enriched in calcium, strontium, large lithophilic elements, and lead, by a mechanism similar to the formation of eclogites in the units of the Western Tien Shan.
Abstract: Cratons represent the oldest preserved lithospheric domains. Their lithosphere (lithospheric mantle welded to overlying Precambrian crystalline basement) is considered to be particularly robust and long living due to the protecting presence of buoyant and rigid “keels” made up of residual harzburgites. In this study, we report new U—Pb zircon ages on crustal xenoliths from the Udachnaya kimberlite in the Siberian craton; this dataset includes samples from both the upper and lower portions of the crust. The zircon ages agree well with model melt-extraction Re-Os ages on refractory peridotite xenoliths from the same pipe; taken together they allow an integrated view of lithosphere formation. Our data reveal that the present day upper crust is Archaean, whereas both the lower crust and the lithospheric mantle yield Palaeoproterozoic ages. Consequently, the deep lithosphere beneath the Siberian craton was not formed in a single time, but grew in two distinct events, one in the late Archean and the other in the Palaeoproterozoic. We propose a two-stage scenario for the formation of the Siberian craton involving delamination and rejuvenation of the Archean lower lithosphere (lower crust and lithospheric mantle) in the Palaeoproterozoic. This demonstrates that craton formation can be a protracted, multi-stage process, and that the present day crust and mantle do not represent complementary reservoirs formed through the same episode.
Abstract: Cratons represent the oldest preserved lithospheric domains. Their lithosphere (lithospheric mantle welded to overlying Precambrian crystalline basement) is considered to be particularly robust and long-lived due to the protecting presence of buoyant and rigid “keels” made up of residual harzburgites. Although the cratons are mostly assumed to form in the Archaean, the timing of their formation remains poorly constrained. In particular, there are very few datasets describing concurrently the age of both the crustal and mantle portions of the lithosphere. In this study, we report new U–Pb ages and Hf isotope compositions for zircons in crustal xenoliths from the Udachnaya kimberlite in the central Siberian craton; this dataset includes samples from both the upper and lower portions of the crust. The zircon ages agree well with model melt-extraction Re–Os ages on refractory peridotite xenoliths from the same pipe; taken together they allow an integrated view of lithosphere formation. Our data reveal that the present day upper crust is Archaean, whereas both the lower crust and the lithospheric mantle yield Paleoproterozoic ages. We infer that the deep lithosphere beneath the Siberian craton was not formed in a single Archaean event, but grew in at least two distinct events, one in the late Archaean and the other in the Paleoproterozoic. Importantly, a complete or large-scale delamination and rejuvenation of the Archaean lower lithosphere (lower crust and lithospheric mantle) took place in the Paleoproterozoic. This further demonstrates that craton formation can be a protracted, multi-stage process, and that the present day crust and mantle may not represent complementary reservoirs formed through the same tectono-magmatic event. Further, deep cratonic lithosphere may be less robust and long living than often assumed, with rejuvenation and replacement events throughout its history.
Abstract: The paper reports the results of an experimental study of phase relations and distribution of elements in silicate melt-salt melt systems (carbonate, phosphate, fluoride, chloride), silicate melt I - silicate melt II, and fluid-magmatic systems in the presence of alkali metal fluorides. Extraction of a number of ore elements (Y, REE, Sr, Ba, Ti, Nb, Zr, Ta, W, Mo, Pb) by salt components was studied in liquid immiscibility processes within a wide temperature range of 800-1250°? and pressure of 1-5.5 kbar. It is shown that partition coefficients are sufficient for concentration of ore elements in amounts necessary for the genesis of ore deposits. In a fluid-saturated trachyrhyolite melt, the separation into two silicate liquids has been determined. The partition coefficients of a number of elements (Sr, La, Nb, Fe, Cr, Mo, K, Rb, Cs) between phases L1 and L2 have been obtained. The interaction processes of a heterophase fluid in the granite (quartz)-ore mineral-heterophase fluid (Li, Na, K-fluoride) system were studied at 650-850°C and P = 1 kbar. The formation of the phase of a highly alkaline fluid-saturated silicate melt concentrating Ta and Nb is shown as a result of the interaction of the fluid with rock and ore minerals.
Abstract: We investigate structure of the mantle transition zone (MTZ) under the central Tien Shan in central Asia by using recordings of seismograph stations in Kyrgyzstan, Kazakhstan and adjacent northern China. We apply P-wave receiver functions techniques and evaluate the differential time between the arrivals of seismic phases that are formed by P to SV mode conversion at the 410-km and 660-km seismic boundaries. The differential time is sensitive to the thickness of the MTZ and insensitive to volumetric velocity anomalies above the 410-km boundary. Under part of the southern central Tien Shan with the lowest S wave velocity in the uppermost mantle and the largest thickness of the crust, the thickness of the MTZ increases by 15-20 km relative to the ambient mantle and the reference model IASP91. The increased thickness is a likely effect of low (about ? 150 K) temperature. This anomaly is indicative of delamination and sinking of the mantle lithosphere. The low temperature in the MTZ might also be a relic of subduction of the oceanic lithosphere in the Paleozoic, but this scenario requires strong coupling and coherence between structures in the MTZ and in the lithosphere during plate motions in the last 300 Myr. Our data reveal a reduction of thickness of the MTZ of 10-15 km under the Fergana basin, in the neighborhood of the region of small-scale basaltic volcanism at the time near the Cretaceous-Paleogene boundary. The reduced thickness of the MTZ is the effect of a depressed 410-km discontinuity, similar to that found in many hotspots. This depression suggests a positive temperature anomaly of about 100-150 K, consistent with the presence of a thermal mantle plume. A similar depression on the 410-km discontinuity is found underneath the Tarim basin.
Geodynamics and Tectonphysics in RUS, Vol. 9, 3, pp. 827-854. only 1 p. english abstract
Africa, Angola
deposit - Catoca
Abstract: This paper presents the first results of the geostructural and tectonophysical studies of the crustal stress state in the Catoca kimberlite pipe area at the southwestern flank of the Kasai Shield in the northeasternAngola. In the evolution of the crustal stress state, six main stages are distinguished by analyzing the displacements of markers, fold hinges, long axes of boudins, granite dikes of various intrusion phases and kimberlites, as well as fractures with striations. For each of these stages, a dominating horizontal tectonic stress and its orientation is identified. During stage 1 (NW extension and shearing) and at the beginning of stage 2 (NW compression), structures formed in the host rocks in brittle-plastic conditions. The replacement of plastic deformation by faulting could occur about 530-510 Ma ago, when the continental crust ofAfricahad completely formed. Stage 3 (radial, mainly NW extension) and stage 4 (shearing, NW extension, and NE compression) were the most important for kimberlite occurrence: in the Early Cretaceous, radial extension was replaced by shearing. Both stages are related to opening of the central segment of theSouth Atlantic. The main kimberlite magmas occurred during the break-up of the Angola-Brazilian segment of Gondwana. In the course of all the four stages, stress was mainly released by the NE- and E-NE-striking faults and, to a lesser extent, by the NW-striking and latitudinal faults. The initial stage of kimberlite magmatism is associated with the NE- and E-NE-striking faults due to the presence of the Precambrian zones of flow and schistosity, which facilitated the NW-trending subhorizontal extension. Stage 5 (NE compression) began in the second half of the Cretaceous and possibly lasted until the end of the Paleogene, and compression occurred mainly along the NW-striking faults. Regionally, it corresponds to two stages of inversion movements in the southern regions of Africa, during which theAngoladome-shaped uplift emerged and the shoulders of the East African rifts began to take shape. Stage 6 (horizontal extension, mainly in the N-NE direction) is related to the processes that took place in the southern segment of theTanganyikarift and the eastern coast of theAtlantic. Based on the results of our studies, it became for the first time possible to get an idea of the main stages in the evolution of the studied region. Further geostructural measurements and dating of the host rocks will provide for a more precise definition of the proposed stages.
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Provenance and reconnaissance study of detrital zircons of the Paleozoic Cape Supergroup: revealing the interaction of Kalahari and Rio de la Plat a cratons.
International Journal of Earth Sciences, Vol. 100, 2, pp. 527-541.
Abstract: Alluvial diamonds from the Kasai River, Democratic Republic of the Congo (DRC) are sourced from Cretaceous kimberlites of the Lucapa graben in Angola. Analysis of 40 inclusion-bearing diamonds provides new insights into the characteristics and evolution of ancient lithospheric mantle of the Congo craton. Silicate inclusions permitted us to classify diamonds as peridotitic, containing Fo91-95 and En92-94, (23 diamonds, 70% of the suite), and eclogitic, containing Cr-poor pyrope and omphacite with 11-27% jadeite (6 diamonds, 18% of the suite). Fluid inclusion compositions of fibrous diamonds are moderately to highly silicic, matching compositions of diamond-forming fluids from other DRC diamonds. Regional homogeneity of Congo fibrous diamond fluid inclusion compositions suggests spatially extensive homogenization of Cretaceous diamond forming fluids within the Congo lithospheric mantle. In situ cathodoluminescence, secondary ion mass spectrometry and Fourier transform infrared spectroscopy reveal large heterogeneities in N, N aggregation into B-centers (NB), and ?13C, indicating that diamonds grew episodically from fluids of distinct sources. Peridotitic diamonds contain up to 2962 ppm N, show 0-88% NB, and have ?13C isotopic compositions from ? 12.5‰ to ? 1.9‰ with a mode near mantle-like values. Eclogitic diamonds contain 14-1432 ppm N, NB spanning 29%-68%, and wider and lighter ?13C isotopic compositions of ? 17.8‰ to ? 3.4‰. Fibrous diamonds on average contain more N (up to 2976 ppm) and are restricted in ?13C from ? 4.1‰ to ? 9.4‰. Clinopyroxene-garnet thermobarometry suggests diamond formation at 1350-1375 °C at 5.8 to 6.3 GPa, whereas N aggregation thermometry yields diamond residence temperatures between 1000 and 1280 °C, if the assumed mantle residence time is 0.9-3.3 Ga. Integrated geothermobaromtery indicates heat fluxes of 41-44 mW/m2 during diamond formation and a lithosphere-asthenosphere boundary (LAB) at 190-210 km. The hotter-than-average cratonic mantle may be attributable to contemporaneous rifting of the southern Atlantic, multiple post-Archean reactivations of the craton, and/or proximal Cretaceous plumes.
Abstract: The results of a study using scanning electron microscopy and atomic force microscopy comprising the micromorphology of the ditrigonal and trigonal layers on surfaces near the edges of octahedral diamond crystals from the Udachnaya-Eastern kimberlite pipe in Yakutia are presented. The studied surface sculptures are elongated parallel to the direction ?111? and have similar morphological features, characterized by a wavy profile across the lamination, the absence of flat areas at the micro- and nanolevel. It is proposed that both sculpture types were formed as a result of dissolution under natural conditions. This suggestion is corroborated by the revelation of negative trigons on the octahedral facets of the studied diamonds.
Abstract: The salt components of aqueous and aqueous-carbonic fluids are very important agents of metasomatism and partial melting of crustal and mantle rocks. The paper presents examples and synthesized data on mineral associations in granulite- and amphibolite-facies rocks of various composition in the middle and lower crust and in upper-mantle eclogites and peridotites that provide evidence of reactions involving salt components of fluids. These data are analyzed together with results of model experiments that reproduce some of these associations and make it possible to more accurately determine their crystallization parameters.
Global and Planetary Change, doi.org/j.gloplacha.2017.10.011 24p.
Africa
geodynamics
Abstract: Modern satellite gravimetry is now considered one of the most powerful and effective instrument for regional tectono-geodynamic zonation. Satellite gravity observations clearly fit the definition of 'big data' because of their volume and variety. The Arabian - NE African region discussed in this article has intricate geodynamic features including active rift zones, high seismic activity and collision processes, a rich structural pattern made up of the mosaic block system of continental and oceanic crusts of different ages, as well as several of the greatest gravity anomalies and complex magnetic anomaly mosaics. This region also has the world's main hydrocarbon resources and a vast number of other economic deposits. A comprehensive analysis of these satellite derived gravity data were used to construct a series of new maps that localize the key properties of the lithosphere of the region. A careful examination of numerous geological sources and their combined inspection with satellite derived gravity and other geophysical data resulted in this new integrated tectonic map of the Arabian-African region. An analysis of the series of gravity map transformations and certain geological indicators document the significant geodynamic features of the region.
Abstract: On the basis of petrographic and mineralogical studies, we have established the presence of clastic rocks with a strong predominance of K-feldspar among the rock-forming fragments within the Late Precambrian sedimentary sequence in the southwestern part of the Siberian Platform. Two types of mineralogical occurrence of K-feldspars are determined: (1) huge zonal crystal clasts with increased Ba concentrations in the central parts of the grains and (2) the main mineral phase in the form of a decrystallized glassy mass. In both cases, low concentrations of Na (lower than 0.1 wt %) are detected. K-feldspars of the second type contain intergrowths of idiomorphic rhombic dolomite with a high ankerite component. Dolomite grains contain inclusions of K-feldspar. The prevailing accessory minerals are F-apatite (with high concentrations of REEs), zircon (with high concentrations of Th), magnetite, rutile, monacite, and sinchizite. Encasement minerals with an idiomorphic shape are identified, with K-feldspar being located in the center, while the middle shell is formed by apatite with a high REE content, and the outer shell is formed by apatite without rare earth elements. These rocks are products of high-potassium volcanic activity. The age of this event has been established on the basis of U-Pb zircon dating to about 640 Ma. The Lu-Hf zircon systematics for these rocks indicates the connection of volcanism with igneous events of mantle genesis within its range. The products of explosive eruption, which are widespread within the Biryusa uplift of the Siberian Platform, were erroneously considered earlier as Riphean sedimentary rocks of the Karagas Series.
Abstract: We have analyzed 141 grains of pyrope from Neogene sediments in a quarry of construction materials, in the Kenkeme River catchment, along its left-side tributary (Chakiya River), about 60 km northwest of Yakutsk city. The mineral chemistry patterns of pyropes are typical of Jurassic-Cretaceous barren kimberlites, like the pipes of Obnazhennaya or Muza, but are uncommon to diamondiferous Middle Paleozoic kimberlites. The results allow identifying the magmatic event and placing time constraints on kimberlite magmatism in the southeastern flank of the Vilui basin, which was part of the Late Jurassic-Early Cretaceous tectonic-magmatic event in northeastern Asia.
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.
Petrochemical interpretation of carbonatite-like rocks from the Chagatai Complex of the Tien Shan with appllication to the problem of diamond potential.
Parameterization of melting regime of shallow upper mantle and effects of variable lithospheric stretching on mantle modal stratification, trace elementmagmas
Geological Society of London Special Publication 513, pp. 45-70.
Russia
lamproites
Abstract: Ingashi lamproite dykes are the only known primary sources of diamond in the Irkutsk district (Russia) and the only non-kimberlitic one in the Siberian craton. The Ingashi lamproite field is situated in the Urik-Iya graben within the Prisayan uplift of the Siberian craton. The phlogopite-olivine lamproites contain olivine, talc, phlogopite, serpentine, chlorite, olivine, garnet, chromite, orthopyroxene, clinopyroxene as well as Sr-F-apatite, monazite, zircon, armolcolite, priderite, potassium Mg-arfvedsonite, Mn-ilmenite, Nb-rutile and diamond. The only ultramafic lamprophyre dyke is composed mainly of serpentinized olivine and phlogopite in the talc-carbonate groundmass and is similar to Ingashi lamproites accessory assemblage with the same major element compositions. Trace element and Sr-Nd isotopic relationships of the Ingashi lamproites are similar to classic lamproites. Different dating methods have provided the ages of lamproites: 1481 Ma (Ar-Ar phlogopite), 1268 Ma (Rb-Sr whole rock) and 300 Ma (U-Pb zircon). Ingashi lamproite ages are controversial and require additional study. The calculated pressure of 3.5 GPamax for clinopyroxenes indicates that lamproite magma originated deeper than 100 km. A Cr-in-garnet barometer shows a 3.7-4.3 GPamin and derivation of Ingashi lamproites deeper than 120 km in depth. Based on the range of typical cratonic geotherms and the presence of diamonds, the Ingashi lamproite magma originated at a depth greater than 155 km.
Abstract: The characteristics of the sub-continental lithospheric mantle (SCLM) post-date the Siberian plume event (250 Ma) is still unclear; nearly all published data for mantle xenoliths are from a single kimberlite erupt before he Siberian plume (Udachnaya). We report major elements of the whole rock, trace elements data of clinopyroxene and Re-Os isotope and PGE concentration of mantle xenoliths from the Obnazhennaya kimberlite pipe (160 Ma). The Obnazhennaya mantle xenoliths, including spinel harzburgites, spinel dunites, spinel lherzolites, spinel-garnet lherzolite. The spinel harzburgites and dunites have refractory compositions, with 0.23-1.35 wt.% Al2O3, 0.41-3.11 wt.% CaO and 0.00-0.09 wt.% TiO2. Clinopyroxenes in harzburgites and dunites have lower Na2O but higher Cr2O3 contents. Modeling of the Y and Yb contents in clinopyroxenes indicates that the spinel harzburgites and dunites have been subjected to ca. 12-17% degrees of partial melting. The spinel harzburgites and dunites have 187Os/188Os of 0.11227-0.11637, giving a TRD age of 1.6-2.2 Ga. This suggests that old cratonic mantle still existed beneath the Obnazhennaya. In contrast, the lherzolites (both spinel- and spinel-garnet-) have more fertile compositions, containing 2.16-6.55 wt.% Al2O3, 2.91-7.55 wt.% CaO and 0.04-0.15 wt.% TiO2. Both spinel and spinelgarnet lherzolites have more radiogenic 187Os/188Os ratios (0.11931-0.17627), enriched P-PGEs. The higher Al2O3 and Os content and depleted IPGE character of these lherzolites suggest that they were not juvenile mantle accreted by Siberian mantle plume but the refertilized ancient mantle. Therefore, our result suggest that the cratonic mantle beneath the Obnazhennaya has not been replaced by juvenile mantle during the Siberian mantle plume.
Abstract: The characteristics of the sub-continental lithospheric mantle (SCLM) post-date the Siberian plume event (250 Ma) is still unclear; nearly all published data for mantle xenoliths are from a single kimberlite erupt before he Siberian plume (Udachnaya). We report major elements of the whole rock, trace elements data of clinopyroxene and Re-Os isotope and PGE concentration of mantle xenoliths from the Obnazhennaya kimberlite pipe (160 Ma). The Obnazhennaya mantle xenoliths, including spinel harzburgites, spinel dunites, spinel lherzolites, spinel-garnet lherzolite. The spinel harzburgites and dunites have refractory compositions, with 0.23-1.35 wt.% Al2O3, 0.41-3.11 wt.% CaO and 0.00-0.09 wt.% TiO2. Clinopyroxenes in harzburgites and dunites have lower Na2O but higher Cr2O3 contents. Modeling of the Y and Yb contents in clinopyroxenes indicates that the spinel harzburgites and dunites have been subjected to ca. 12-17% degrees of partial melting. The spinel harzburgites and dunites have 187Os/188Os of 0.11227-0.11637, giving a TRD age of 1.6-2.2 Ga. This suggests that old cratonic mantle still existed beneath the Obnazhennaya. In contrast, the lherzolites (both spinel- and spinel-garnet-) have more fertile compositions, containing 2.16-6.55 wt.% Al2O3, 2.91-7.55 wt.% CaO and 0.04-0.15 wt.% TiO2. Both spinel and spinelgarnet lherzolites have more radiogenic 187Os/188Os ratios (0.11931-0.17627), enriched P-PGEs. The higher Al2O3 and Os content and depleted IPGE character of these lherzolites suggest that they were not juvenile mantle accreted by Siberian mantle plume but the refertilized ancient mantle. Therefore, our result suggest that the cratonic mantle beneath the Obnazhennaya has not been replaced by juvenile mantle during the Siberian mantle plume.
Geological Society of London Special Publication 513, pp. 71-102.
Russia, Siberia
deposit - Muna
Abstract: Petrographic, geochemical and mineralogical characteristics of diamond deposits from the Upper Muna field have been investigated. Geochemically, diamondiferous kimberlites from Upper Muna belong to the most widespread Fe-Mg-rich rocks in the Yakutian kimberlite province (average FeOtotal = 8.4 wt%, MgO = 32.36 wt%, TiO2 = 1.6 wt%). Striking mineralogical features of Upper Muna kimberlites are: (1) abundance of monticellite and perovskite in the groundmass; (2) rare occurrence of Mg-ilmenite; (3) abundance of phlogopite megacrysts (up to 8 cm across); and (4) coexistence of low-Cr (0.1-4 wt% Cr2O3, with 0.8-1.2 wt% TiO2) and high-Cr (3-8 wt% Cr2O3, with 0.1-0.6 wt% TiO2) garnet megacrysts with contrasting rare earth element patterns. The compositional features of groundmass minerals, the relatively low CaO and CO2 contents in kimberlites and few deuteric alteration in Upper Muna kimberlites suggest high-temperature melt crystallization during pipe emplacement. Based on the compositional data of garnet and Cr-diopside from megacrysts and peridotites, we suggest a poor Cr dunite-harzburgitic and lherzolitic mantle source beneath the Upper Muna field where Cr-diopside crystallized within a wide pressure and temperature range (40-65 kbar and 900-1350°?). The mineral geochemistry, trace element distribution and Sr-Nd isotope variations of Upper Muna kimberlites are typical for group I kimberlites and reflect a deep-seated asthenospheric (convective mantle) source for the kimberlites.
Geological Society of London Special Publication 513, pp. 71-102.
Russia, Siberia
deposit - Muna
Abstract: Petrographic, geochemical and mineralogical characteristics of diamond deposits from the Upper Muna field have been investigated. Geochemically, diamondiferous kimberlites from Upper Muna belong to the most widespread Fe-Mg-rich rocks in the Yakutian kimberlite province (average FeOtotal = 8.4 wt%, MgO = 32.36 wt%, TiO2 = 1.6 wt%). Striking mineralogical features of Upper Muna kimberlites are: (1) abundance of monticellite and perovskite in the groundmass; (2) rare occurrence of Mg-ilmenite; (3) abundance of phlogopite megacrysts (up to 8 cm across); and (4) coexistence of low-Cr (0.1-4 wt% Cr2O3, with 0.8-1.2 wt% TiO2) and high-Cr (3-8 wt% Cr2O3, with 0.1-0.6 wt% TiO2) garnet megacrysts with contrasting rare earth element patterns. The compositional features of groundmass minerals, the relatively low CaO and CO2 contents in kimberlites and few deuteric alteration in Upper Muna kimberlites suggest high-temperature melt crystallization during pipe emplacement. Based on the compositional data of garnet and Cr-diopside from megacrysts and peridotites, we suggest a poor Cr dunite-harzburgitic and lherzolitic mantle source beneath the Upper Muna field where Cr-diopside crystallized within a wide pressure and temperature range (40-65 kbar and 900-1350°?). The mineral geochemistry, trace element distribution and Sr-Nd isotope variations of Upper Muna kimberlites are typical for group I kimberlites and reflect a deep-seated asthenospheric (convective mantle) source for the kimberlites.
Ashchepkov, I., Ntaflos, T., Logvinova, A., Vladykin, N., Ivanov, A., Spetsius, Z., Stegnitsky, Y., Kostrovitsky, S., Salikhov, R., Makovchuk, I., Shmarov, G., Karpenko, M., Downes, H., Madvedev, N.
Abstract: The PTX diagrams for the separate phases in Sytykanskaya (Ashchepkov et al., 2016) Dalnyaya (Ashchepkov et al., 2017), pipes shows that the PK show the relatively simple P-X trends and geotherms and shows more contrast and simple layering. The PK contain most abundant material from the root of the magma generation they are dunitic veins as the magma feeders represented by the megacrysts. New results for the Aykhal, Zarya and Komsomolskaya pipes in Alake field and Zarnitsa and Udachnaya pipes in Daldyn field show that evolution is accompanied by the developing of metasomatites and branching and veining of the wall rock peridotites . In Aykhal pipe in PK the Gar- dunites prevail, the xenoliths from the dark ABK "Rebus" contain Cr-Ti - rich garnets and ilmenites, more abundant compared with the grey carbonited breccia Nearly the same features were found for Yubileinaya pipe. The example of Komsomolskya pipes show that the ABK contain more eclogitic xenolith than PK. The developing of the magma channel shown in satellite Chukukskaya and Structurnaya pipe was followed by the separation of some parts of the magmatic feeders and crystallization of abundant Gar megacrysts near o the walls blocking the peridotites from the magma feeder. This drastically decrease diamond grade of pipes. Such blocking seems to be the common features for the latest breccias. In Zarnitsa pipe, the dark PK and ABK also contain fresh xenoliths but not only dunites but also sheared and metasomatic varieties and eclogites. Most of dark ABK in Yakutia contain the intergrowth of ilmenites with brown Ti- Cpx showing joint evolution trends. The late breccia contains completely altered peridotite xenoliths mainly of dunite- harzburgite type. The comparison of the trace elements of the coexisting minerals in megacryst show that they were derived from the protokimberlites but are not in complete equilibrium as well as other megacrystalline phases. Ilmenites show inflections of the trace element patterns of most Ilmenites but more regular for the Cpx and Garnets revealing the sub parallel patterns elevating LREE with the rising TRE. But commonly these are not continuous sequances because they developed in the pulsing moving systems like beneath Zarnitsa. The minerals from the feeders like dunites also show the inflected or S-type REE patterns. From the earlier to later phases the TRE compositions became more evolved reflecting the evolution of protokimberlites. The wall rocks also often show the interaction with the more evolved melts and sometimes "cut" spectrums due to the dissolution some phases and repeated melting events So we could suggest the joint evolution of the mantle column protokimberlites and megacrysts composition and type of kimberlites with the diamond grade. The mantle lithospheric base captured by the PK. The developing and rising protokimbelrites was followed by the crystallization of the diamonds in the gradient in FO2 zone in wall rocks due to reductions of C -bearing fluids and carbonatites (> 1 QMF) on peridotites ((< -2 -5 QMF). The most intensive reactions are near the graphite - diamond boundary where protokimberlites are breaking and where most framesites are forming.
European Journal of Mineralogy, doi.org./ 101127/ejm/2018/0030-2783 cost $ 30.00 US
Russia
deposit - Daldyn
Abstract: The spatial distribution patterns of Mg-bearing ilmenite (Ilm) composition were studied on 54 kimberlite bodies of the Daldyn field in the Yakutian kimberlite province. The representativity of the ilmenites sampled in this study is ensured by analysing ca. 100 grains from each kimberlite body. The major conclusions are as follows: (1) ilmenites from neighbouring pipes within the same linear cluster have similar average compositions and compositional fields on the MgO-Cr2O3 plots; (2) ilmenites from different clusters of pipes show different average compositions and compositional fields on the MgO-Cr2O3 plots. (3) regardless of belonging to different clusters, low-Mg Ilm across the whole Daldyn field is characterized by a direct correlation between Al2O3 and MgO; (4) significant changes of MgO content are observed in high-Mg Ilm, while Al2O3 content remains at the same level. The similarity of Ilm compositions across the kimberlite field, as shown by the MgO-Al2O3 plots, is due to a common asthenospheric source. The similar Ilm compositions in different bodies within cluster of pipes is accounted for by a single supply of magma via a lithospheric mantle channel for all pipes of the cluster. The composition of the kimberlite melts can be altered owing to the incorporation and assimilation of lithospheric mantle rocks rich in Mg and Cr. These changes of the melt cause corresponding changes in the Ilm macrocryst composition, both during and after crystallization of Ilm. Thus, the Ilm macrocryst composition follows a trend from low-Mg/low-Cr for Ilm crystallizing in the asthenosphere, to high-Mg/high-Cr at higher levels in the lithosphere. The key conclusion of this study is that Ilm can be used to decipher the structure of kimberlite fields. This can provide a reliable geological criterion for grouping an association of pipes together in clusters, which were previously identified only through subjective considerations of the spatial proximity of kimberlite bodies.
European Journal of Mineralogy, Vol. 30, 6, pp. 1083-1094.
Russia, Yakutia
deposit - Dalydyn
Abstract: The spatial distribution patterns of Mg-bearing ilmenite (Ilm) composition were studied on 54 kimberlite bodies of the Daldyn field in the Yakutian kimberlite province. The representativity of the ilmenites sampled in this study is ensured by analysing ca. 100 grains from each kimberlite body. The major conclusions are as follows: (1) ilmenites from neighbouring pipes within the same linear cluster have similar average compositions and compositional fields on the MgO-Cr2O3 plots; (2) ilmenites from different clusters of pipes show different average compositions and compositional fields on the MgO-Cr2O3 plots. (3) regardless of belonging to different clusters, low-Mg Ilm across the whole Daldyn field is characterized by a direct correlation between Al2O3 and MgO; (4) significant changes of MgO content are observed in high-Mg Ilm, while Al2O3 content remains at the same level. The similarity of Ilm compositions across the kimberlite field, as shown by the MgO-Al2O3 plots, is due to a common asthenospheric source. The similar Ilm compositions in different bodies within cluster of pipes is accounted for by a single supply of magma via a lithospheric mantle channel for all pipes of the cluster. The composition of the kimberlite melts can be altered owing to the incorporation and assimilation of lithospheric mantle rocks rich in Mg and Cr. These changes of the melt cause corresponding changes in the Ilm macrocryst composition, both during and after crystallization of Ilm. Thus, the Ilm macrocryst composition follows a trend from low-Mg/low-Cr for Ilm crystallizing in the asthenosphere, to high-Mg/high-Cr at higher levels in the lithosphere. The key conclusion of this study is that Ilm can be used to decipher the structure of kimberlite fields. This can provide a reliable geological criterion for grouping an association of pipes together in clusters, which were previously identified only through subjective considerations of the spatial proximity of kimberlite bodies.
Contributions to Mineralogy and Petrology, Vol. 175, 22p. Pdf.
Russia
deposit - Obnazhennaya
Abstract: The petrology, mineral major and trace-element concentrations, and garnet oxygen isotopic composition of low-MgO (11-16 wt%) eclogites from the Obnazhennaya kimberlite, Siberian craton, are used to infer their petrogenesis. These eclogites contain two types of compositionally distinct garnet: granular coarse garnet, and garnet exsolution (lamellae and fine-grained garnet) in clinopyroxene. The former record higher temperatures at lower pressures than the latter, which record the last stage of equilibrium at moderate pressure-temperature conditions 2.3-3.7 GPa and 855-1095 °C in the upper mantle at the time of entrainment. Although derived from the garnet stability field, these rocks have low-pressure cumulate protoliths containing plagioclase, olivine, and clinopyroxene as reflected by pronounced positive Eu and Sr anomalies in all eclogites, and low heavy rare earth element (HREE) contents in both minerals and reconstructed bulk rocks for a number of samples. Major elements, transition metals, and the HREE compositions of the reconstructed whole rocks are analogous to modern oceanic gabbro cumulates. Despite geochemical signatures supporting an oceanic crust origin, mantle-like ?18O of the garnets (5.07-5.62‰) for most samples indicates that the protoliths either did not interact with seawater or have coincidently approximately normal igneous values. Some of the eclogite xenoliths have lower SiO2 contents and depleted light REE ((Nd/Yb)N?1) compared to modern oceanic gabbros, suggesting that they experienced partial melting. Positively inclined middle to heavy REE patterns ((Dy/Yb)N?1) of the reconstructed bulk rocks mostly result from repeated partial melting in the eclogite stability field, based on melting model calculations. We, therefore, suggest that the Obnazhennaya low-MgO eclogites may represent the gabbroic section of subducted or foundered basaltic crust that underwent continued partial melting processes at high pressures, where garnet was the main residual phase.
The exceptionally fresh Udachnaya-East kimberlite: evidence from brine and evaporite contamination.
Proceedings of the 10th. International Kimberlite Conference, Vol. 1, Special Issue of the Journal of the Geological Society of India,, Vol. 1, pp. 75-91.
Repeated kimberlite magmatism beneath Yakutia and its relationship to Siberian flood volcanism: insights from in situ U-Pb and Sr-Nd perovskite isotope analysis.
Earth and Planetary Science Letters, Vol. 404, Oct. pp. 283-295.
Russian Geology and Geophysics, Vol. 56, pp. 1701-1716.
Russia
Deposit - Grib
Abstract: New data on metasomatic processes in the lithospheric mantle in the central part of the Arkhangelsk diamondiferous province (ADP) are presented. We studied the major- and trace-element compositions of minerals of 26 garnet peridotite xenoliths from the V. Grib kimberlite pipe; 17 xenoliths contained phlogopite. Detailed mineralogical, petrographic, and geochemical studies of peridotite minerals (garnet, clinopyroxene, and phlogopite) have revealed two types of modal metasomatic enrichment of the lithospheric-mantle rocks: high temperature (melt) and low-temperature (phlogopite). Both types of modal metasomatism significantly changed the chemical composition of the peridotites. Low-temperature modal metasomatism manifests itself as coarse tabular and shapeless phlogopite grains. Two textural varieties of phlogopite show significant differences in chemical composition, primarily in the contents of TiO2, Cr2O3, FeO, Ba, Rb, and Cs. The rock-forming minerals of phlogopite-bearing peridotites differ in chemical composition from phlogopite-free peridotites, mainly in higher FeO content. Most garnets and clinopyroxenes in peridotites are the products of high-temperature mantle metasomatism, as indicated by the high contents of incompatible elements and REE pattern in these minerals. Fractional-crystallization modeling gives an insight into the nature of melts (metasomatic agents). They are close in composition to picrites of the Izhmozero field, basalts of the Tur’ino field, and carbonatites of the Mela field of the ADP. The REE patterns of the peridotite minerals make it possible to determine the sequence of metasomatic enrichment of the lithospheric mantle beneath the V. Grib kimberlite pipe.
Abstract: Comprehensive studies of zircon xenocrysts from kimberlites of the Kuoika field (northeastern Siberian craton) and several kimberlite fields of the eastern Anabar shield, along with data compilation on the age of kimberlite-hosting terranes, reveal details of the evolution of the northern Siberian craton. The age distribution and trace element characteristic of zircons from the Kuoika field kimberlites (Birekte terrane) provide evidence of significant basic and alkaline-carbonatite magmatism in northern Siberia in the Paleozoic and Mesozoic periods. The abundance of 1.8-2.1 Ga zircons in both the Birekte and adjacent Hapchan terranes (the latter hosting kimberlites of the eastern Anabar shield) supports the Paleoproterozoic assembly and stabilization of these units in the Siberian craton and the supercontinent Columbia. The abundance of Archean zircons in the Hapchan terrane reflects the input of an ancient source other than the Birekte terrane and addresses the evolution of the terrane to west (Magan and Daldyn terranes of the Anabar shield). The present study has also revealed the oldest known remnant of the Anabar shield crust, whose 3.62 Ga age is similar to that of the other ancient domain of Siberia, the Aldan shield. The first Hf isotope data for the Anabar shield coupled with the U-Pb systematics indicate three stages of crustal growth (Paleoproterozoic, Neoarchean and Paleoarchean) and two stages of the intensive crustal recycling in the Paleoproterozoic and Neoarchean. Intensive reworking of the existing crust at 2.5-2.8 Ga and 1.8-2.1 Ga is interpreted to provide evidence for the assembly of Columbia. The oldest Hf model age estimation provides a link to Early Eoarchean (3.7-3.95 Ga) and possibly to Hadean crust. Hence, some of the Archean cratonic segments of the Siberian craton could be remnants of the Earth's earliest continental crust.
Journal of Volcanology and Geothermal Research, in press available 19p.
Russia
Deposit - Udachnaya East
Abstract: The Udachnaya East kimberlite is characterized by the presence of chlorides, sulfates and alkali carbonates. This highly atypical mineralogy underpinned a model for an anhydrous alkali-rich primary kimberlite melt, despite the absence of petrographic studies providing textural context to the exotic minerals. The present work documents the petrography of the Udachnaya East kimberlite in order to address this problem. The pipe comprises two varieties of Fort-a-la-Corne type pyroclastic kimberlite, olivine-rich and magmaclast-rich, and coherent kimberlite. These kimberlites entrain xenoliths of limestones, altered shales and siltstones, halite-dominated rocks, dolomites, and coarse calcite rocks. The distinct varieties of the Udachnaya East kimberlite carry different populations of crustal xenoliths, which partially control the mineralogy of the host kimberlite. In magmaclast-rich pyroclastic kimberlite, where halite is absent from the crustal xenoliths, it is not observed in the interclast matrix, or within the magmaclasts. Halite occurs in the interclast matrix of olivine-rich pyroclastic kimberlite, where halite xenoliths are common. Large, ~ 30 cm halite xenoliths are uniquely restricted to the coherent kimberlite and show a strong reaction with it. The halite xenoliths are sourced from depths of ? 1500 to ? 630 m, where carbonate beds host multiple karst cavities filled with halite and gypsum and occasional sedimentary evaporites. The style of secondary mineralization at Udachnaya depends on whether the kimberlite is coherent or pyroclastic. Shortite, pirssonite and other alkali carbonates replacing calcite and possibly serpentine are abundant only in porous pyroclastic kimberlites of both types and in their shale/siltstone xenoliths. The lower porosity of the coherent kimberlite prevented the interaction of kimberlite with Na brines. Serpentinization localized around halite xenoliths started at temperatures above 500 °C, as indicated by its association with high-temperature iowaite. The model of the “dry” Na and Cl-rich primary kimberlite melt is invalidated on the basis of 1) the restriction of exotic salt minerals to certain kimberlite types and xenoliths; and 2) the absence of halite-rich melt inclusions in olivine of coherent kimberlite.
Abstract: Mineral data from Yakutian kimberlites allow reconstruction of the history of lithospheric mantle. Differences occur in compositions of mantle pyropes and clinopyroxenes from large kimberlite pipes in the Alakit and Daldyn fields. In the Alakit field, Cr-diopsides are alkaline, and Stykanskaya and some other pipes contain more sub-calcic pyropes and dunitic-type diamond inclusions, while in the Daldyn field harzburgitic pyropes are frequent. The eclogitic diamond inclusions in the Alakit field are sharply divided in types and conditions, while in the Daldyn field they show varying compositions and often continuous Pressure-Temperature (P-T) ranges with increasing Fe# with decreasing pressures. In Alakit, Cr-pargasites to richterites were found in all pipes, while in Daldyn, pargasites are rare Dalnyaya and Zarnitsa pipes. Cr-diopsides from the Alakit region show higher levels of light Rare Earth Elements (LREE) and stronger REE-slopes, and enrichment in light Rare Earth Elements (LREE), sometimes Th-U, and small troughs in Nb-Ta-Zr. In the Daldyn field, the High Field Strength Elements HFSE troughs are more common in clinopyroxenes with low REE abundances, while those from sheared and refertilized peridotites have smooth patterns. Garnets from Alakit show HREE minima, but those from Daldyn often have a trough at Y and high U and Pb. PTXfO2 diagrams from both regions show similarities, suggesting similar layering and structures. The degree of metasomatism is often higher for pipes which show dispersion in P-Fe# trends for garnets. In the mantle beneath Udachnaya and Aykhal, pipes show 6-7 linear arrays of P-Fe# in the lower part of the mantle section at 7.5-3.0 GPa, probably reflecting primary subduction horizons. Beneath the Sytykanskaya pipe, there are several horizons with opposite inclinations which reflect metasomatic processes. The high dispersion of the P-Fe# trend indicating widespread metasomatism is associated with decreased diamond grades. Possible explanation of the differences in mineralogy and geochemistry of the mantle sections may relate to their tectonic positions during growth of the lithospheric keel. Enrichment in volatiles and alkalis possibly corresponds to interaction with subduction-related fluids and melts in the craton margins. Incorporation of island arc peridotites from an eroded arc is a possible scenario.
Abstract: The modal metasomatic alteration for lithosphere mantle may be investigated using mantle xenoliths from kimberlite pipes. The mantle xenoliths from upper-Jurassic Obnajennaya kimberlite pipe (Kuoika field, Yakutia) were studied. Three main xenoliths groups in Obnajennaya pipe were distinguished based on the petrographic and geochemical features: 1. Sp, Sp-Grt, Grt harzburgites - lherzolites, Sp, Sp-Grt, Grt olivine websterites and Sp, Sp-Grt, Grt websterite (so-called magnesium group - about 80 % from xenoliths). The high magnesium mineral composition, high estimated temperature (1250 - 1500°?) for exsolution pyroxene megacrystals, presence of sulphide globules and distribution curves for rare earth elements in garnets (La-Yb increasing) are to assume the crystallisation from melt. The 10% magnesium mantle xenoliths are observed the secondary metasomatic phlogopite and amphibole (pargasite). The clinopyroxene distribution curves demonstrate the wide range of values and altered samples show higher content HFSE group elements that primary clinopyroxene. The increasing of HFSE and rare earth element concentrations can also be traced by the amphibole chemical composition. The 40Ar/39Ar dating of phlogopite from was result 1639 ± 5 Ma nearly corresponding to the time of Siberian craton accretion Thus during Siberian craton accretion (about 1.7 Ga) the melts-fluids enriching Nb + Ta and REE impacted on lithosphere mantle under Kuoika field. 2. Eclogites and Grt clinopyroxenites with similar mineral composition (about 10-15% xenoliths). The high ?O18 for garnet and clinopyroxene (5.7–5.8‰) allows to assume subduction genesis. 3. Phl-Ilm rocks characterizing ferrous mineral composition (~ 10 % xenoliths). This group are charactetrized are ferrous mineral composition. The 40Ar/39Ar phlogopite dating resulted to 800-500 Ma, signed the potassium and titanium metasomatic fluide – melt influenced
Formation and evolution of hypabyssal kimberlites from the Siberian craton: part 1 - new insights from cathodluminescence of the carbonates. Anabar and Olenek area
Journal of Asian Earth Sciences, Vol. 145, pt. B, pp. 670-678.
Abstract: A comprehensive, internally consistent U-Pb and Lu-Hf isotope data set for 93 mantle-derived zircons from the Yakutian kimberlite province confirms and further refines the four major episodes of kimberlite magmatism on the Siberian craton: 421-409?Ma (Late Silurian-Early Devonian), 358-353?Ma (Late Devonian-Early Carboniferous), 226-218?Ma (Late Triassic), and 161-144?Ma (Middle-Late Jurassic). The relatively narrow, constant range of ?Hf values between +2 and +10 for both the Paleozoic and Mesozoic mantle-derived zircons (and by inference kimberlites) suggests that the volatile-rich magmas were repeatedly sourced from the convecting upper mantle beneath the Siberian craton. This finding is in keeping with the narrow and constant range of ?Nd values for groundmass perovskites from the Yakutian kimberlite province between +1.8 and +5.5 between 420 and 150?Ma. Our preferred model implies that the convecting upper mantle beneath the Yakutian kimberlite province ‘recovered’ rapidly back to ambient conditions shortly after the giant plume-related flood volcanic event that produced the Siberian Traps at 250?Ma. Although close spatial relationships exist between kimberlites and flood basalts on the Siberian craton during both the Paleozoic and Mesozoic, exact timing of the igneous events and the isotopic compositions of the diverse deep-sourced melting products rule out any direct genetic links.Besides the highly economic kimberlite-hosted diamond deposits of Late Devonian age (e.g., Mir and Udachnaya), the Siberian craton also contains significant Mesozoic placer diamond deposits (e.g., along the Anabar river), for which lamproite sources have been suggested recently. Our study shows that mantle-derived zircon megacryst fragments from the Ebelyakh placer deposit have Late Triassic ages of ca. 224?Ma. Their long-term depleted Hf isotopic compositions (+8.5 ?Hf) suggest that the alluvial diamonds were sourced from asthenosphere-derived Triassic kimberlites rather than from lithospheric mantle derived isotopically enriched lamproites.
Abstract: A comprehensive, internally consistent U-Pb and Lu-Hf isotope data set for 93 mantle-derived zircons from the Yakutian kimberlite province confirms and further refines the four major episodes of kimberlite magmatism on the Siberian craton: 421-409?Ma (Late Silurian-Early Devonian), 358-353?Ma (Late Devonian-Early Carboniferous), 226-218?Ma (Late Triassic), and 161-144?Ma (Middle-Late Jurassic). The relatively narrow, constant range of ?Hf values between +2 and +10 for both the Paleozoic and Mesozoic mantle-derived zircons (and by inference kimberlites) suggests that the volatile-rich magmas were repeatedly sourced from the convecting upper mantle beneath the Siberian craton. This finding is in keeping with the narrow and constant range of ?Nd values for groundmass perovskites from the Yakutian kimberlite province between +1.8 and +5.5 between 420 and 150?Ma. Our preferred model implies that the convecting upper mantle beneath the Yakutian kimberlite province ‘recovered’ rapidly back to ambient conditions shortly after the giant plume-related flood volcanic event that produced the Siberian Traps at 250?Ma. Although close spatial relationships exist between kimberlites and flood basalts on the Siberian craton during both the Paleozoic and Mesozoic, exact timing of the igneous events and the isotopic compositions of the diverse deep-sourced melting products rule out any direct genetic links. Besides the highly economic kimberlite-hosted diamond deposits of Late Devonian age (e.g., Mir and Udachnaya), the Siberian craton also contains significant Mesozoic placer diamond deposits (e.g., along the Anabar river), for which lamproite sources have been suggested recently. Our study shows that mantle-derived zircon megacryst fragments from the Ebelyakh placer deposit have Late Triassic ages of ca. 224?Ma. Their long-term depleted Hf isotopic compositions (+8.5 ?Hf) suggest that the alluvial diamonds were sourced from asthenosphere-derived Triassic kimberlites rather than from lithospheric mantle derived isotopically enriched lamproites.
Abstract: A comprehensive, internally consistent U-Pb and Lu-Hf isotope data set for 93 mantle-derived zircons from the Yakutian kimberlite province confirms and further refines the four major episodes of kimberlite magmatism on the Siberian craton: 421-409?Ma (Late Silurian-Early Devonian), 358-353?Ma (Late Devonian-Early Carboniferous), 226-218?Ma (Late Triassic), and 161-144?Ma (Middle-Late Jurassic). The relatively narrow, constant range of ?Hf values between +2 and +10 for both the Paleozoic and Mesozoic mantle-derived zircons (and by inference kimberlites) suggests that the volatile-rich magmas were repeatedly sourced from the convecting upper mantle beneath the Siberian craton. This finding is in keeping with the narrow and constant range of ?Nd values for groundmass perovskites from the Yakutian kimberlite province between +1.8 and +5.5 between 420 and 150?Ma. Our preferred model implies that the convecting upper mantle beneath the Yakutian kimberlite province ‘recovered’ rapidly back to ambient conditions shortly after the giant plume-related flood volcanic event that produced the Siberian Traps at 250?Ma. Although close spatial relationships exist between kimberlites and flood basalts on the Siberian craton during both the Paleozoic and Mesozoic, exact timing of the igneous events and the isotopic compositions of the diverse deep-sourced melting products rule out any direct genetic links. Besides the highly economic kimberlite-hosted diamond deposits of Late Devonian age (e.g., Mir and Udachnaya), the Siberian craton also contains significant Mesozoic placer diamond deposits (e.g., along the Anabar river), for which lamproite sources have been suggested recently. Our study shows that mantle-derived zircon megacryst fragments from the Ebelyakh placer deposit have Late Triassic ages of ca. 224?Ma. Their long-term depleted Hf isotopic compositions (+8.5 ?Hf) suggest that the alluvial diamonds were sourced from asthenosphere-derived Triassic kimberlites rather than from lithospheric mantle derived isotopically enriched lamproites.
Abstract: The article describes the petrography and mineralogy of xenoliths ilmenite-phlogopite containing deformed and granular peridotites from the Udachnaya-Eastern pipe. The age of pholopite porphyroclast from the studied deformed xenoliths matches with age of Phl megacryst and itself hosted kimberlites from Udachnaya pipe indicating the following processes closed in time: (1) crystallization of the low-Cr megacryst association; (2) deformation of rocks on the mantle lithosphere-asthenosphere border during the kimberlite-forming cycle; (3) formation of protokimberlite melts.
Abstract: Variations of the structure and composition of mantle terranes in the terminology of the Siberian craton were studied using database (>60000) EPMA of kimberlite xenocrysts from the pipes of Yakutian kimberlite province (YKP) by a team of investigators from IGM, IGH, IEC and IGBM SB RAS and ALROSA company. The monomineral thermobarometry (Ashchepkov et al., 2010, 2014, 2017) Geochemistry of minerals obtained LA ICP MS was used to determine the protolith, melting degree, Type of the metasomatism . The mantle stratification commonly was formed by 6-7 paleosubduction slabs, separated by pyroxenite, eclogite, and metasomatic horizons and dunite lenses beneath kemberltes . We built mantle sections across the kimberlite field and transects of craton. Within the established tectonic terrains strengthening to thousands km (Gladkochub et al, 2006), the collage of microplates was determined at the mantle level. Under the shields of Anabar and Aldan lower SCLM consist of 3 -4 dunites dunites with Gar-Px-Ilm- Phl nests. Terranes framing protocratons like suture Khapchanskyare are saturated in eclogites and pyroxenites, sometimes dominated probably represent the ascending bodies of igneous eclogites intruding mantle lithosphere (ML). The ubiquitous pyroxenite layer at the level of 3.5-4.5 GPa originated in the early Archaean when melted eclogites stoped stoped subdction. Beneath the Early Archaean granite-greenstone terranes - Tunguskaya, Markhinskaya, Birektinskaya, Shary-Zhalgaiskaya (age to~3.8-3.0 GA) (Gladkochub et al., 2018) the SCLM is less depleted and often metasomatized having flat structures in some subterrains. Daldyn and Magan granulite-orthogneisic terranes have a layered and folded ML seen in N-S sections from Udachnaya to Krasnopresnenskaya less pronounced in latitudinal direction. From Daldyn to Alakit field increases the degree of Phl metasomatism and Cpx alkalinity. The most productive Aykhal and Yubleynaya pipes confined to the dunite core. Within the Magan terrane, the thin-layered SCLM have depleted base horizon. Granite-greenstone Markha terrane contains pelitic eclogites. Central and Northern craton parts show slight inclination of paleoslabs to West. The formation of SCLM in Hadean accompanied by submelting (Perchuk et al., 2018, Gerya, 2014.) had no deep roots. Ultrafine craton nuclei like Anabar shield was framed by steeper slab. During 3.8-3.0 GA craton keel growth in superplume periods (Condie, 2004) when melted eclogites and peridotites acquiring buoyancy of the sinking plate melted. For peridotites, the melting lines calculated from the experimental data (Herzberg, 2004) mainly lie near 5-6 GPA (Ionov et al., 2010; 2015). In classical works all geotherms are conductive (Boyd, 1973), but this is quite rare. The garnet pyroxene geotherms for (Ashchepkov et al., 2017) calculated with most reliable methods (Nimis, Taylor, 2000; McGregor , 1974; Brey Kohler, Nickel Green, 1985; Ashchepkov et al., 2010; 2017) give are sub-adiabatic and are formed during the melt percolation superplume vent often in presence of volatiles (Wyllie, Ryabchikov, 2000) and therefore, after superplumes trends P-Fe# of garnet are smoothed and change the tilts.
Abstract: The article by Abersteiner et al., (2018) discussing the mantle origin of salts in serpentine-free kimberlites from the Udachnaya-East pipe contradicts the views of Kostrovitsky et al. (2013) concerning the origin of these salts from a surface source of brines. Here we wish to emphasize that Abersteiner et al. (2018) have presented erroneous statements regarding the genesis of these rocks. On the basis of the data collected by hydrogeologists working at Udachnaya-East we consider that unaltered kimberlites occur at 400-500 m depth, where the brines precipitated salts. The relation of unaltered kimberlites to the surface sources of salt is illustrated by the cross sections of the Mir and International’naya pipes, where serpentine-free kimberlites occur at the depths of Cambrian evaporite host rocks intercalated with thick halite layers. It is assumed that the salts from surface sources prevented olivine serpentinization. The secondary origin of salts in serpentine-free kimberlites is confirmed by our investigations and the hypothesis regarding the mantle origin of salts is doubtful.
Abstract: We present new major element geochemical data, and review the existing data for ilmenite macrocrysts, megacrysts, as well as ilmenite in mantle xenoliths from four diamondiferous kimberlite fields in the Yakutian province. This combined data set includes 10,874 analyses of ilmenite from 94 kimberlite pipes. In the studied samples we identify various different ilmenite compositional distributions (e.g., “Haggerty's parabola”, or “Step-like” trends in MgO-Cr2O3 bivariate space), which are common to all kimberlites from a given cluster, but the compositional distributions differ between clusters. We propose three stages of ilmenite crystallization: 1) Mg-Cr poor ilmenite crystallising from a primitive asthenospheric melt (the base of Haggerty's parabola on MgO-Cr2O3 plots). 2) This primitive asthenospheric melt was then modified by the partial assimilation of lithospheric material, which enriched the melt in MgO and Cr2O3 (left branch of Haggerty’s parabola). 3) Ilmenite subsequently underwent sub-solidus recrystallization in the presence of an evolved kimberlite melt under increasing oxygen fugacity (ƒO2) conditions (right branch of Haggerty’s parabola in MgO-Cr2O3 plots). Significant differences in the ilmenite compositional distribution between different kimberlite fields are the result of diverse conditions during subsequent ilmenite crystallization in a kimberlite melt ascending through the lithospheric mantle, which have different textures and compositions beneath the studied kimberlite fields. We propose that a TiO2 fluid formed due to immiscibility of an asthenospheric melt with low Cr and high Ti contents. This fluid infiltrated lithospheric mantle rocks forming Mg-ilmenite. These features indicate a genetic link between ilmenite and the host kimberlite melt.
Abstract: This study concerns the geochemical characteristics of mantle xenoliths from the upper-Jurassic Obnazhennaya kimberlite pipe (Kuoika field, Yakutian kimberlite province, the north-east of Siberian craton). The so-called magnesian xenolith group (Sp, Sp-Grt, Grt lherzolites, olivine websterites and websterites) was distinguished, the rocks of the group are assumed to be of the same genesis based on transitions in modal mineral composition and a change in the composition of minerals. The chemical composition (CaO, MgO) of most depleted harzburgites, as well as part of the lherzolites of the magnesian group coincide with the restites obtained by experimental melting, which suggested their residue origin. Narrow variations in the composition of olivine (Mg # - 91-92; NiO - 0.35-0.45 wt.%) and orthopyroxene (Mg # - 92-93) for Obnazhennaya peridotites also support this hypothesis. In terms of chemical composition, olivines coincide with the “mantle trend” of olivines from the lithospheric mantle. Nevertheless, garnets from the peridotites consistently change their composition in the direction of decreasing Cr2O3, CaO and Mg # values from Grt, Sp-Grt lherzolites to Grt websterites. The garnet composition from Obnazhennaya peridotites differs from Udachnaya peridotites, for which the residue hypothesis assumed. They are similar in composition to garnets from Beni-Bousera garnet pyroxenites, as well as to garnets from deformed lherzolites of the Udachnaya pipe, which suggests crystallization of garnets from the melt and the effect of metasomatic processes. The formation of orogenic massifs is a multi-stage process, many authors suggest that pyroxenite veins in mafic complexes are cumulative in origin and show signs of metasomatic processes (in particular, enrichment with aluminum, calcium and chromium, increased REE concentrations in garnet). So peridotite cumulative origin and further metasomatic transformations were suggested.
Abstract: The petrology, mineral major and trace element concentrations, and garnet oxygen isotopic composition of low-MgO (11-16 wt.%) eclogites from the Obnazhennaya kimberlite, Siberian craton, are used to infer their petrogenesis. These eclogites equilibrated at moderate pressure-temperature conditions 2.3-3.7 GPa and 855- 1095?C at the time of entrainment. Although derived from the garnet stability field, these rocks have low-pressure cumulate protoliths containing plagioclase, olivine, and clinopyroxene as reflected by pronounced positive Eu and Sr anomalies in all eclogites, and low heavy rare earth element (HREE) contents in both minerals and reconstructed bulk rocks for a number of samples. Major elements, transition metals, and the HREE compositions of the reconstructed whole rocks are analogous to modern oceanic gabbro cumulates. Despite geochemical signatures supporting an oceanic crust origin, mantle-like ?18O of the garnets (5.07-5.62 ‰ ) for most samples indicates that the protoliths either did not interact with seawater or have coincidently approximately normal igneous values. Some of the eclogite xenoliths have lower SiO2 contents and depleted light REE ((Nd/Yb)N ? 1) compared to modern oceanic gabbros, suggesting that they experienced partial melting. Positively inclined middle to heavy-REE patterns ((Dy/Yb)N ?1) of the reconstructed bulk rocks mostly result from repeated partial melting in the eclogite stability field, based on melting model calculations. We therefore suggest that the Obnazhennaya low-MgO eclogites may represent the gabbroic section of subducted or foundered basaltic crust that underwent continued partial melting processes at high pressures where garnet was the main residual phase.
Russian Geology and Geophysics, Vol. 62, pp. 605-618.
Russia
deposit - Aikhal
Abstract: A dike of rock similar in composition to carbonatites has been found in the Aikhal diamondiferous pipe of the Alakit-Markha field of the Yakutian kimberlite province (YaKP). The fine-grained rock of essentially carbonate composition (dolomite and calcite) rich in thin-platy phlogopite contains minerals typical of carbonatites: monazite, baddeleyite, and pyrochlore. In the high contents and distribution of incompatible elements the rock differs significantly from kimberlites and is transitional from kimberlites to carbonatites. The content of incompatible elements in this rock is 3-5 times lower than that in carbonatite breccias of the pipes in the Staraya Rechka kimberlite field of the YaKP (Nomokhtookh site). The compositions of accessory trace element minerals from the Aikhal dike rock and the Nomokhtookh carbonatite breccias are compared. An assumption is made that the high contents of incompatible elements in the carbonatite-like rock, which caused the crystallization of accessory minerals, are due to the differentiation of kimberlite melt/fluid. The high Sr isotope ratios indicate that the rock altered during hydrothermal and metasomatic processes. The obtained data on the composition of the carbonatite-like rock cannot serve as an argument for the genetic relationship between the Aikhal kimberlites and typical carbonatites. The genetic relationship between kimberlites and carbonatites in the northern fields of the YaKP remains an open issue.
International Geology Review, Vol. 64, 8, pp. 1119-1138.
Russia, Siberia
kimberlite magmatism
Abstract: Zircon xenocrysts from two diamond-barren kimberlite pipes (Leningrad and Ruslovaya) in the West Ukukit kimberlite field opened a ‘window’ to the buried crustal basement in the northern Siberian craton. Zircon U-Pb ages reveal a close affinity of the basement of the Khapchan belt to the Archaean Anabar province and a significant tectonomagmatic reworking in the Paleoproterozoic (~2.1-1.8 Ga) due to collision between the Anabar province and the Olenek province. The West Ukukit kimberlite field experienced multiple tectonomagmatic reactivation from ~670 to 144 Ma, which can be attributed to interaction of the deep crust with mantle-derived melts. Hf isotope composition of zircon xenocrysts reveals significant addition of juvenile material into the crust during the Paleoproterozoic orogeny in diamond-barren kimberlite fields, which is different from the reworking crust in the southern Yakutia diamondiferous kimberlite fields. Eruption of the Leningrad and Ruslovaya pipes were constrained as the Late Jurassic, much later than the well-known Late Silurian-Earth Devonian kimberlites in the West Ukukit kimberlite field. A NE-trending, >2000 km long kimberlite corridor is proposed to account for a prolonged lithospheric channel for episodic eruption of kimberlites in the Siberian craton. The diamond storage in the lithosphere beneath the West Ukukit kimberlite field may have been largely reduced by the Paleoproterozoic orogeny and Phanerozoic reworking.
Abstract: The petrochemistry of carbonatites of three formation types were studied: (1) ultrahigh-pressure garnet-containing carbonatites (UHPC) of the Caledonian sheet (Tromsö, Norway); (2) rocks of the carbonatite-lkaline-ultrabasic Kovdor massif (the Kola Peninsula); and (3) rocks of the carbonatite-alkaline-gabbroid Tikshozero massif (north of Karelia). The samples of carbonatites were examined and tested with a microprobe; the microelements were determined using the ICP-MS technique at the Institute of Microelectronics Technology and High Purity Materials (Chernogolovka). The carbonatites of the Kovdor and Tikshozero massifs are characterized by similar negative REE trends, with a degree of REE enrichment of the Tikshozero carbonatites. The UHPC from Tromsö are different from those of the Kovdor and Tikshozero massifs in the negative trend along with lower concentrations of light REEs. The Tromsö UHPC are similar to the carbonatites of the Kovdor and Tikshozero massifs in the trend and concentrations of heavy REEs. The carbonatites of the Fennoscandian shield of various formation times and types are characterized by the geochemical similarity to those in different regions of the world with the sources associated to mantle plumes. This similarity might be caused by the formation of the mantle carbonated magmas of carbonatite-containing igneous complexes from a mantle source enriched under either mantle metasomatism or plume-lithosphere interaction, with similar mechanisms of formation. The appearance of the formations as such within a wide time interval points to the long-term occurrence of a superplume at the Fennoscandian shield and to permanent activation of the related processes of magma formation.
Abstract: This study presents geochemical data on organic-rich rock samples collected from Riphean—Lower Paleozoic strata (potential source rocks) of the southern Siberian Platform and compositional data on hydrocarbon biomarkers (steranes, terpanes, n-alkanes, 12- and 13-methylalkanes, isoprenanes) and diamondoid hyrocarbons from core samples collected from the Kulindinskaya-1 well, which was drilled by RN-Exploration in 2012 within the Katanga saddle.
Geochemistry International, Vol. 59, 8, pp. 801-812. pdf
Europe, Norway
deposit - Tromso Nappe
Abstract: The paper presents data on phase relations in garnet-bearing carbonatite from the Tromsø Nappe, Norway. The carbonatite matrix consists of calcite-dolomite carbonate with three generations of garnet inclusions (up to 15-20%). The relics of the primary garnets (Grt1) are depleted (<10-2 wt %) in the rare earth elements (REE). The garnet of the second and third generations (Grt2-3) is anomalously enriched (up to 10-15 wt %) in the light REE (LREE), and the carbonates are depleted in these elements. The distribution of REE between the garnet and carbonate indicates the absence of equilibrium. The melting of the carbonatite at T = 950-1400°C, P = 4.0 GPa showed that the “dry” solidus temperature is 1150°C, and the liquidus temperature is >1300°C. In the experiment with H2O + CO2 fluid, the solidus and liquidus temperatures are ?950 and 1250°C, respectively. The subsolidus association is calcite, garnet, clinopyroxene, biotite, and accessory minerals: apatite, ilmenite, rutile, and titanite. The garnet and carbonatite melt occur in reaction relationships, as is evident from the garnet zoning with a decrease in the FeO and increase in the MgO, CaO, TiO2, and LREE concentrations. The geological setting, phase relationships, and experimental data indicate that the garnet-bearing carbonatites in the Tromsø area were formed in relation to the carbonatization and melting of upper mantle material at high pressures during the collision of the Baltica and Laurentia plates in the course of the Caledonian orogenesis, with subsequent intrusion and crystallization of silicate-carbonate magmas.
A venture into the interior of natural diamond genetic information and implications for the gem industry. Part 1, the main types of internal growth structures.
Abstract: The paper reports the results of an experimental study of phase relations and distribution of elements in silicate melt-salt melt systems (carbonate, phosphate, fluoride, chloride), silicate melt I - silicate melt II, and fluid-magmatic systems in the presence of alkali metal fluorides. Extraction of a number of ore elements (Y, REE, Sr, Ba, Ti, Nb, Zr, Ta, W, Mo, Pb) by salt components was studied in liquid immiscibility processes within a wide temperature range of 800-1250°? and pressure of 1-5.5 kbar. It is shown that partition coefficients are sufficient for concentration of ore elements in amounts necessary for the genesis of ore deposits. In a fluid-saturated trachyrhyolite melt, the separation into two silicate liquids has been determined. The partition coefficients of a number of elements (Sr, La, Nb, Fe, Cr, Mo, K, Rb, Cs) between phases L1 and L2 have been obtained. The interaction processes of a heterophase fluid in the granite (quartz)-ore mineral-heterophase fluid (Li, Na, K-fluoride) system were studied at 650-850°C and P = 1 kbar. The formation of the phase of a highly alkaline fluid-saturated silicate melt concentrating Ta and Nb is shown as a result of the interaction of the fluid with rock and ore minerals.
Abstract: The paper reports the results of an experimental study of phase relations and distribution of elements in silicate melt-salt melt systems (carbonate, phosphate, fluoride, chloride), silicate melt I - silicate melt II, and fluid-magmatic systems in the presence of alkali metal fluorides. Extraction of a number of ore elements (Y, REE, Sr, Ba, Ti, Nb, Zr, Ta, W, Mo, Pb) by salt components was studied in liquid immiscibility processes within a wide temperature range of 800-1250°? and pressure of 1-5.5 kbar. It is shown that partition coefficients are sufficient for concentration of ore elements in amounts necessary for the genesis of ore deposits. In a fluid-saturated trachyrhyolite melt, the separation into two silicate liquids has been determined. The partition coefficients of a number of elements (Sr, La, Nb, Fe, Cr, Mo, K, Rb, Cs) between phases L1 and L2 have been obtained. The interaction processes of a heterophase fluid in the granite (quartz)-ore mineral-heterophase fluid (Li, Na, K-fluoride) system were studied at 650-850°C and P = 1 kbar. The formation of the phase of a highly alkaline fluid-saturated silicate melt concentrating Ta and Nb is shown as a result of the interaction of the fluid with rock and ore minerals.
Journal of The Geological Society of India, Vol. 87, 2, pp. 127-131.
India
Lamproite
Abstract: A singular outcrop of a lamproite dyke is located ~1.5 km south-west of Chintalapalle village at the NW margin of the Cuddapah basin, eastern Dharwar craton, southern India.. The dyke trends E-W and is emplaced within the granitic rocks belonging to the peninsular gneissic complex. The lamproite dyke has a porphyritic to weakly porphyritic texture comprising microphenocrysts of sanidine, and potassic richterite set in a groundmass rich in carbonate, and chlorite with rutile and titanate as accessory phases. This new occurrence of lamproite is located mid-way between the well-known Narayanpet kimberlite field towards the west and the Ramadugu and Vattikod lamproite fields in east. The Chintalapalle lamproite dyke, together with those from Vattikod, Ramadugu, Krishna and Cuddapah basin lamproite fields, constitute a wide spectrum of ultrapotassic magmatism emplaced in and around the Palaeo-Mesoproterozoic Cuddapah basin in southern India.
Contributions to Mineralogy and Petrology, Vol. 173, 12, pp. 106-
Mantle
metasomatism
Abstract: Multiphase solid inclusions in minerals formed at ultra-high-pressure (UHP) provide evidence for the presence of fluids during deep subduction. This study focuses on barian mica, which is a common phase in multiphase solid inclusions enclosed in garnet from mantle-derived UHP garnet peridotites in the Saxothuringian basement of the northern Bohemian Massif. The documented compositional variability and substitution trends provide constraints on crystallization medium of the barian mica and allow making inferences on its source. Barian mica in the multiphase solid inclusions belongs to trioctahedral micas and represents a solid solution of phlogopite KMg3(Si3Al)O10(OH)2, kinoshitalite BaMg3(Al2Si2)O10(OH)2 and ferrokinoshitalite BaFe3(Al2Si2)O10(OH)2. In addition to Ba (0.24-0.67 apfu), mica is significantly enriched in Mg ( X Mg 0.85 to 0.95), Cr (0.03-0.43 apfu) and Cl (0.04-0.34 apfu). The substitution vector involving Ba in the I-site which describes the observed chemical variability can be expressed as BaFeIVAlClK-1Mg-1Si-1(OH)-1. A minor amount of Cr and VIAl enters octahedral sites following a substitution vector VI(Cr,Al)2?VI(Mg,Fe)-3 towards chromphyllite and muscovite. As demonstrated by variable Ba and Cl contents positively correlating with Fe, barian mica composition is partly controlled by its crystal structure. Textural evidence shows that barian mica, together with other minerals in multiphase solid inclusions, crystallized from fluids trapped during garnet growth. The unusual chemical composition of mica reflects the mixing of two distinct sources: (1) an internal source, i.e. the host peridotite and its garnet, providing Mg, Fe, Al, Cr, and (2) an external source, represented by crustal-derived subduction-zone fluids supplying Ba, K and Cl. At UHP-UHT conditions recorded by the associated diamond-bearing metasediments (c. 1100 °C and 4.5 GPa) located above the second critical point in the pelitic system, the produced subduction-zone fluids transporting the elements into the overlying mantle wedge had a solute-rich composition with properties of a hydrous melt. The occurrence of barian mica with a specific chemistry in barium-poor mantle rocks demonstrates the importance of its thorough chemical characterization.
Russian Journal of Pacific Geology, Vol. 11, 6, pp. 447-468.
Russia
picrites
Abstract: A great volume of original information on the formation of the ultrabasic rocks of the Siberian Platform has been accumulated owing to the study of melt inclusions in Cr-spinels. The inclusions show the general tendencies in the behavior of the magmatic systems during the formation of the ultrabasic massifs of the Siberian Platform, tracing the main evolution trend of decreasing Mg number with SiO2 increase in the melts with subsequent transition from picrites through picrobasalts to basalts. The compositions of the melt inclusions indicate that the crystallization conditions of the rocks of the concentrically zoned massifs (Konder, Inagli, Chad) sharply differ from those of the Guli massif. Numerical modeling using the PETROLOG and PLUTON softwares and data on the composition of inclusions in Cr-spinels yielded maximum crystallization temperatures of the olivines from the dunites of the Konder (1545-1430°C), Inagli (1530-1430°C), Chad (1460-1420°C), and Guli (1520-1420°C) massifs, and those of Cr-spinels from the Konder (1420-1380°C), Inagli (up to 1430°C), Chad (1430-1330°C), and Guli (1410-1370°C) massifs. Modeling of the Guli massif with the PLUTON software using the compositions of the melt inclusions revealed the possible formation of the alkaline rocks at the final reverse stage of the evolution of the picritic magmas (with decrease of SiO2 and alkali accumulation) after termination of olivine crystallization with temperature decrease from 1240-1230°C to 1200-1090°C. Modeling with the PLUTON software showed that the dunites of the Guli massif coexisted with Fe-rich (with moderate TiO2 contents) melts, the crystallization of which led (beginning from 1210°C) to the formation of pyroxenes between cumulate olivine. Further temperature decrease (from 1125°C) with decreasing FeO and TiO2 contents provided the formation of clinopyroxenes of pyroxenites. For the Konder massif, modeling with the PLUTON software indicates the possible formation of kosvites from picrobasaltic magmas beginning from 1350°C and the formation of clinopyroxenites and olivine-diopside rocks from olivine basaltic melts from 1250°C.
Abstract: 40Ar/39Ar analysis showed a simultaneous (at about 490 Ma) formation of the Paleozoic picrite and basalt complexes of the West Siberian Plate basement. The petrochemistry, trace and REE geochemistry, and composition of clinopyroxene indicate the formation of the picrite of well no. 11 (Chkalov area) as a result of intraplate magmatism of the OIB type. Calculations based on the compositions of clinopyroxene allowed crystallization of minerals of porphyric picrite at 1215-1275°C and 4.5-8 kbar. In general, it has been found that the picrite basalt complexes considered were formed from enriched igneous plume systems under intraplate conditions near the active margin of the ancient ocean.
Kovach, V.,Salnikova, E., Wang, K-L., Jahn, B-M., Chiu, H-Y., Reznitskiy, L., Kotov, A., Lizuka, Y., Chung, S-L.
Zircon ages and Hf isotopic constraints on sources of clastic metasediments of the Slyudyansky high grade complex, southeastern Siberia: implication for continental growth and evolution of the Central Asian orogenic belt.
Journal of Asian Earth Sciences, Vol. 62, pp. 18-36.
Korikovsky, S., Kotov, A., Salnikova, E., Aranovich, L., Korpechkov, D., Yakovleva, S., Tolmacheva, E., Anisimova, I.
The age of the protolith of metamorphic rocks in the southeastern Lapland granulite belt, southern Kola Peninsula: correlation with the Belomorian mobile belt in the context of the problem of Archean eclogites.
Age of formation of apocarbonate metasomites of the Sharyzhalgai Uplift of the Siberian Craton basement, southwestern Baikal region U - Pb baddeleyite, zircon
Doklady Earth Sciences, Vol. 399A, 9, Nov-Dec. pp. 1204-1208.
Abstract: We report new geological, mineralogical, geochemical and geochronological data about the Katugin Ta-Nb-Y-Zr (REE) deposit, which is located in the Kalar Ridge of Eastern Siberia (the southern part of the Siberian Craton). All these data support a magmatic origin of the Katugin rare-metal deposit rather than the previously proposed metasomatic fault-related origin. Our research has proved the genetic relation between ores of the Katugin deposit and granites of the Katugin complex. We have studied granites of the eastern segment of the Eastern Katugin massif, including arfvedsonite, aegirine-arfvedsonite and aegirine granites. These granites belong to the peralkaline type. They are characterized by high alkali content (up to 11.8?wt% Na2O?+?K2O), extremely high iron content (FeO?/(FeO??+?MgO)?=?0.96-1.00), very high content of most incompatible elements - Rb, Y, Zr, Hf, Ta, Nb, Th, U, REEs (except for Eu) and F, and low concentrations of CaO, MgO, P2O5, Ba, and Sr. They demonstrate negative and CHUR-close ?Nd(t) values of 0.0…?1.9. We suggest that basaltic magmas of OIB type (possibly with some the crustal contamination) represent a dominant part of the granitic source. Moreover, the fluorine-enriched fluid phases could provide an additional source of the fluorine. We conclude that most of the mineralization of the Katugin ore deposit occurred during the magmatic stage of the alkaline granitic source melt. The results of detailed mineralogical studies suggest three major types of ores in the Katugin deposit: Zr mineralization, Ta-Nb-REE mineralization and aluminum fluoride mineralization. Most of the ore minerals crystallized from the silicate melt during the magmatic stage. The accessory cryolites in granites crystallized from the magmatic silicate melt enriched in fluorine. However, cryolites in large veins and lens-like bodies crystallized in the latest stage from the fluorine enriched melt. The zircons from the ores in the aegirine-arfvedsonite granite have been dated at 2055?±?7?Ma. This age is close to the previously published 2066?±?6?Ma zircon age of the aegirine-arfvedsonite granites, suggesting that the formation of the Katugin rare-metal deposit is genetically related to the formation of peralkaline granites. We conclude that Katugin rare-metal granites are anorogenic. They can be related to a Paleoproterozoic (?2.05?Ga) mantle plume. As there is no evidence of the 2.05?Ga mantle plume in other areas of southern Siberia, we suggest that the Katugin mineralization occurred on the distant allochtonous terrane, which has been accreted to Siberian Craton later.
Abstract: Mantle xenoliths from the Middle-Late Jurassic Obnazhennaya kimberlite are often compared with those from the Udachnaya kimberlite (ca. 367 Ma) to inform the evolution of the Siberia craton. However, there are no direct constraints on the timing of the Obnazhennaya kimberlite eruption. Such uncertainty of the kimberlite age precludes a better understanding of the mantle xenoliths from the Obnazhennaya pipe, and thus also of the evolution of the Siberia craton. This paper reports U-Pb ages for both perovskite from the Obnazhennaya kimberlite and rutile in an Obnazhennaya eclogite xenolith. The fresh perovskite formed during the early stage of magmatic crystallization and yields a U-Pb age of 151.8 ± 2.5 Ma (2?). Rutile in the eclogite xenolith yields an overlapping U-Pb age of 154.2 ± 1.9 Ma (2?). Because rutile has a Pb closure temperature lower than the inferred residence temperature of the eclogite prior to eruption, the U-Pb isotope system in rutile was not closed until the host eclogite was entrained and delivered to the surface by the kimberlite and therefore records the timing of kimberlite eruption. These data provide the first direct constraints on the emplacement age of the Obnazhennaya kimberlite and add to the global ‘kimberlite bloom’ from ca. 250-50 Ma as well as to the largest pulse of kimberlite volcanism in Siberia from ca. 171-144 Ma. The timing of this Jurassic-Cretaceous pulse coincides with the closure of the Mongol-Okhotsk Ocean, but the depleted Sr-Nd isotopic characteristics of 171-144 Ma kimberlites are inconsistent with a subduction-driven model for their petrogenesis. Thus, the closure of the Mongol-Okhotsk Ocean may act as a trigger for the initiation of 171-144 Ma kimberlite emplacement of Siberia, but was not the source.
Abstract: Exhumed ultrahigh-pressure (UHP) terranes, involving slices of deeply subducted crustal rocks, provide unique material for studying material transfer in subduction zones. Diamond-bearing UHP rocks with sedimentary protoliths allow for tracing melting processes at both UHP and UHT including carbon cycling in the Earth. We studied microdiamonds and associated phases in two contrasting lithologies, (1) acid, quartzofeldpathic UHP gneiss composed of garnet, kyanite, feldspar, quartz and biotite, with a high ASI characteristic of sedimentary rocks, and (2) intermediate garnet-clinopyroxene rock containing quartz, feldspar, minor kyanite and biotite, which is metaluminous. Whereas rock (1) contains exclusively single octahedral diamonds with perfect crystal shape in garnet, kyanite (more common) and zircon, the microdiamonds in the rock (2) occur mostly as clusters of cuboid shape in garnet and zircon. Micro-Raman and FIB TEM data document presence of graphite, quartz and rutile at diamond/host interface or in separate multiple solid inclusions (MSI) whereas carbonates are practically absent. The morphology and lack of inclusions reflect relatively slow growth of the octahedral diamonds (rock 1) at lower fluid supersaturation. Individual deep and symmetrical negative trigons (AFM) on the (111) plane suggest dissolution by a residual silicate-carbonate melt. In contrast, polycrystallline character of diamond cuboids (rock 2) along with their common dissolution and formation of numerous tetragonal etch pits reflect relatively rapid growth of these grains from highly supersaturated fluid/melt. Peak P-T conditions for the UHP rocks of ? 1100ºC at 4.5 GPa are located above the phengite dehydration melting curve, where silicate melts are produced and may coexist with carbonate melts. In view of the light carbon isotope composition and lack of carbonates, we suggest that the diamonds crystallized from the graphitized primordial organic matter under reducing conditions at presence of silicate melt.
Abstract: This manuscript presents results of the newest petrographic, mineralogical and bulk chemical, as well as H, C and O stable isotope study of carbonatites and associated silicate rocks from the Tajno Massif (NE Poland). The Tajno Intrusion is a Tournaisian-Visean ultramafic-alkaline-carbonatite body emplaced within the Paleoproterozoic rocks of the East European Craton (EEC). Carbonatites of the Tajno Massif can be subdivided into the calciocarbonatite (calcite), ferrocarbonatite (ankerite), and breccias with an ankerite-fluorite matrix. Due to location at the cratonic margin and abundance in the REE, Tajno classifies (Hou et al., 2015) as the carbonatite-associated REE deposit (CARD), and more precisely as the Dalucao-Style orebody (the breccia-hosted orebody). High Fe2O3 (13.8 wt%), MnO (2.1 wt%), total REE (6582 ppm), Sr (43895 ppm), Ba (6426 ppm), F (greater than10000 ppm) and CO2 contents points for the involvement of the slab - including pelagic metalliferous sediments - in the carbonatites formation. Spatial relations and Sr isotope composition ((87Sr/86Sr)i = 0.7043-0.7048; Wiszniewska et al., 2020) of alkali clinopyroxenite and syenite suggest that these are products of differentiation of the magma, generated by the initial melting of the SCLM due to influx of F-rich fluids from subducted marine sediments. Carbonatites Sr isotope composition ((87Sr/86Sr)i = 0.7037-0.7038), and Ba/Th (16-20620) and Nb/Y (0.01-6.25) ratios, link their origin with a more advanced melting of the SCLM, triggered by CO2-rich fluids from the subducted AOC and melts from sediments. The Tajno Massif - and coeval mafic-alkaline intrusions - age, high potassic composition, and location along the craton margin nearly parallel the Variscan deformation front, are suggesting Variscan subduction beneath the EEC. The oxygen isotope compositions of clinopyroxene (?18O value = 5.2‰) and alkali feldspar (?18O value = 5.7‰), from alkali clinopyroxenite and foid syenite, respectively, are consistent with mantle-derived magmas. Isotopic compositions of carbonatites and breccias (carbonate ?18O = 8.7‰ to 10.7‰; ?13C = -4.8‰ to ?0.4‰) span from values of primary carbonatites to carbonatites affected by a fractionation or sedimentary contamination. The highest values (?18O = 10.7‰; ?13C = -0.4‰) were reported for breccia cut by numerous veins confirming post-magmatic hydrothermal alteration. The lowest carbonate ?18O (9.3‰ to 10.7‰) and ?13C (?5.0‰ to ?3.8‰) values are reported for veins in alkali clinopyroxenites, whereas the highest ?18O (11.2‰) and ?13C (?1.2‰ to ?1.1‰) values are for veins in syenites and trachytes. Isotopic composition of veins suggests hydrothermal origin, and interaction with host mantle-derived rocks, as well as country rocks. In silicate rocks of the Tajno Massif, fluid influx leads to the development of Pb, Zn, Cu, Ag, Au sulfide mineralization-bearing stockwork vein system, with carbonate, silicate and fluorite infilling the veins. Bulk-rock contents of molybdenum (925 ppm), rhenium (905 ppb) and palladium (29 ppb) are notable. The Re-rich molybdenite association with galena, pyrite and Th-rich bastnäsite in carbonate veins is similar as in Mo deposits associated with carbonatites, implying the mantle source of Mo and Re.
Earth and Planetary Science Letters, Vol. 558, 115763, 6p. Pdf
Europe, Italy
UHP
Abstract: The stabilization of coesite is a diagnostic indicator of ultrahigh-pressure metamorphism and in many cases it implies that a rock has been subducted to a minimum depth of 80 km. Coesite typically occurs as rare relicts in rigid host minerals, but most commonly transforms into ?-quartz pseudomorphs during exhumation. The abundance of coesite-bearing rocks in orogens worldwide is a contentious issue in the petrological community, despite evidence from numerical modeling that suggests that coesite formation should be a common geological process during ultrahigh-pressure metamorphism. This knowledge gap must be addressed to improve the understanding of the geological aspects of subduction-zone geodynamics. Here we report that minuscule coesites (<20 ?m) occur as abundant inclusions in garnet-rich layers from the Italian Western Alps. The discovery of such intact inclusions may fill the gaps in the predicted and observed abundances of coesite worldwide. Through integrated approaches with resolutions down to the nano-scale, we show that these garnet-hosted inclusions are composed entirely of coesite. Our results suggest that common coesite-derived quartz pseudomorphs are less typical structures in ultrahigh-pressure metamorphic rocks and the minuscule coesite in many rocks may be overlooked because of its size. These findings open up new research directions for constraining the extent of deeply subducted rocks and their rheology.
Abstract: The interaction of hydrous fluids and melts with dry rocks of the lithospheric mantle inevitably modifies their viscoelastic and chemical properties due to the formation of compositionally distinct secondary phases. In addition, melt percolation and the associated metasomatic alteration of mantle rocks may also facilitate modification of the pre-existing rock texture and olivine crystallographic preferred orientation (CPO) and thus seismic properties. Here we explore the relationship between mantle metasomatism, deformation and seismic anisotropy using subduction-related mantle xenoliths from the Penghu Islands, western Taiwan. The investigated xenoliths have equilibrated at upper lithospheric mantle conditions (879?°C to 1127?°C) based on pyroxene geothermometry and show distinct variations in clinopyroxene chemical composition, texture and olivine CPO allowing for the classification of two distinct groups. Group 1 xenoliths contain rare earth element (REE) depleted clinopyroxene, show a porphyroclastic texture and olivine grains are mostly characterized by [100]-axial pattern symmetries. In contrast, REE-enriched clinopyroxene from Group 2 xenoliths occur in a fine-grained equigranular texture and coexisting olivine frequently displays [010]-axial pattern symmetries. The clinopyroxene compositions are indicative of cryptic and modal to stealth metasomatic alteration of Group 1 and Group 2 xenoliths, respectively. Furthermore, the observed olivine [100]-axial pattern of Group 1 xenoliths reflects deformation by dislocation creep at high temperature, low pressure and dry conditions, whereas olivine [010]-axial patterns of Group 2 xenoliths imply activation of olivine [001] glide planes along preferentially wet (010) grain boundaries. This correlation indicates that the variation in olivine CPO symmetry from [100]- to [010]-axial pattern in Penghu xenoliths results from deformation and intra-crystalline recovery by subgrain rotation during metasomatic alteration induced by melt percolation. The microstructural observations and olivine CPO combined with petrological and geochemical data suggest that Group 1 xenoliths preserve microstructural and chemical characteristics of an old, probably Proterozoic lithosphere, while Group 2 xenoliths record localized Miocene deformation associated with wall-rock heating and metasomatism related to melt circulation. Furthermore, the observed transition of olivine CPO from [100]-axial pattern to [010]-axial pattern by deformation in the presence of variable melt fractions and associated metasomatic alteration can be inferred to modify the physical properties of mantle rocks.
Abstract: The interaction of hydrous fluids and melts with dry rocks of the lithospheric mantle inevitably modifies their viscoelastic and chemical properties due to the formation of compositionally distinct secondary phases. In addition, melt percolation and the associated metasomatic alteration of mantle rocks may also facilitate modification of the pre-existing rock texture and olivine crystallographic preferred orientation (CPO) and thus seismic properties. Here we explore the relationship between mantle metasomatism, deformation and seismic anisotropy using subduction-related mantle xenoliths from the Penghu Islands, western Taiwan. The investigated xenoliths have equilibrated at upper lithospheric mantle conditions (879?°C to 1127?°C) based on pyroxene geothermometry and show distinct variations in clinopyroxene chemical composition, texture and olivine CPO allowing for the classification of two distinct groups. Group 1 xenoliths contain rare earth element (REE) depleted clinopyroxene, show a porphyroclastic texture and olivine grains are mostly characterized by [100]-axial pattern symmetries. In contrast, REE-enriched clinopyroxene from Group 2 xenoliths occur in a fine-grained equigranular texture and coexisting olivine frequently displays [010]-axial pattern symmetries. The clinopyroxene compositions are indicative of cryptic and modal to stealth metasomatic alteration of Group 1 and Group 2 xenoliths, respectively. Furthermore, the observed olivine [100]-axial pattern of Group 1 xenoliths reflects deformation by dislocation creep at high temperature, low pressure and dry conditions, whereas olivine [010]-axial patterns of Group 2 xenoliths imply activation of olivine [001] glide planes along preferentially wet (010) grain boundaries. This correlation indicates that the variation in olivine CPO symmetry from [100]- to [010]-axial pattern in Penghu xenoliths results from deformation and intra-crystalline recovery by subgrain rotation during metasomatic alteration induced by melt percolation. The microstructural observations and olivine CPO combined with petrological and geochemical data suggest that Group 1 xenoliths preserve microstructural and chemical characteristics of an old, probably Proterozoic lithosphere, while Group 2 xenoliths record localized Miocene deformation associated with wall-rock heating and metasomatism related to melt circulation. Furthermore, the observed transition of olivine CPO from [100]-axial pattern to [010]-axial pattern by deformation in the presence of variable melt fractions and associated metasomatic alteration can be inferred to modify the physical properties of mantle rocks.
Kouyate, D., Soderlund, U., Youbi, N., Ernst, R., Hafid, A., Ikeene, M., Soulaimani, A., Betrand, H., El Janati, M., Rkha, C.
U Pb baddeleyite and zircon ages of 2040 Ma, 1650 Ma and 885 Ma on dolerites in the West African Craton ( Anti-Atlas inliers) : possible links to break up of Precambrian supercontinents.
Youbi, N., Kouyate, D., Soderlund, U., Ernst, R.E., Soulaimani, A., Hafid, A., Ikenne, M., El Bahat, A., Betrand, H., Chaham, K.R., Ben Abbou, M., Mortaji, A., El Ghorfi, M., Zouhair, M., El Janati, M.
The 1750 Ma magmatic event of the West African Craton ( Anti-Atlas) Morocco.
Abstract: We report new geological, mineralogical, geochemical and geochronological data about the Katugin Ta-Nb-Y-Zr (REE) deposit, which is located in the Kalar Ridge of Eastern Siberia (the southern part of the Siberian Craton). All these data support a magmatic origin of the Katugin rare-metal deposit rather than the previously proposed metasomatic fault-related origin. Our research has proved the genetic relation between ores of the Katugin deposit and granites of the Katugin complex. We have studied granites of the eastern segment of the Eastern Katugin massif, including arfvedsonite, aegirine-arfvedsonite and aegirine granites. These granites belong to the peralkaline type. They are characterized by high alkali content (up to 11.8?wt% Na2O?+?K2O), extremely high iron content (FeO?/(FeO??+?MgO)?=?0.96-1.00), very high content of most incompatible elements - Rb, Y, Zr, Hf, Ta, Nb, Th, U, REEs (except for Eu) and F, and low concentrations of CaO, MgO, P2O5, Ba, and Sr. They demonstrate negative and CHUR-close ?Nd(t) values of 0.0…?1.9. We suggest that basaltic magmas of OIB type (possibly with some the crustal contamination) represent a dominant part of the granitic source. Moreover, the fluorine-enriched fluid phases could provide an additional source of the fluorine. We conclude that most of the mineralization of the Katugin ore deposit occurred during the magmatic stage of the alkaline granitic source melt. The results of detailed mineralogical studies suggest three major types of ores in the Katugin deposit: Zr mineralization, Ta-Nb-REE mineralization and aluminum fluoride mineralization. Most of the ore minerals crystallized from the silicate melt during the magmatic stage. The accessory cryolites in granites crystallized from the magmatic silicate melt enriched in fluorine. However, cryolites in large veins and lens-like bodies crystallized in the latest stage from the fluorine enriched melt. The zircons from the ores in the aegirine-arfvedsonite granite have been dated at 2055?±?7?Ma. This age is close to the previously published 2066?±?6?Ma zircon age of the aegirine-arfvedsonite granites, suggesting that the formation of the Katugin rare-metal deposit is genetically related to the formation of peralkaline granites. We conclude that Katugin rare-metal granites are anorogenic. They can be related to a Paleoproterozoic (?2.05?Ga) mantle plume. As there is no evidence of the 2.05?Ga mantle plume in other areas of southern Siberia, we suggest that the Katugin mineralization occurred on the distant allochtonous terrane, which has been accreted to Siberian Craton later.
Kovach, V.,Salnikova, E., Wang, K-L., Jahn, B-M., Chiu, H-Y., Reznitskiy, L., Kotov, A., Lizuka, Y., Chung, S-L.
Zircon ages and Hf isotopic constraints on sources of clastic metasediments of the Slyudyansky high grade complex, southeastern Siberia: implication for continental growth and evolution of the Central Asian orogenic belt.
Journal of Asian Earth Sciences, Vol. 62, pp. 18-36.
Abstract: The Os-isotope compositions of sulphides in mantle xenoliths hosted by Late Miocene alkali basalts from the Sviyaginsky volcano, Russian Far East, reveal the presence of Archaean-Proterozoic subcontinental lithospheric mantle beneath the Khanka massif. Their TMA and TRD model ages reveal similar peaks at 1.1 and 0.8 Ga suggesting later thermotectonic events in the subcontinental lithospheric mantle, whereas TRD model ages range back to 2.8 ± 0.5 (2?) Ga. The events recognized in the subcontinental lithospheric mantle are consistent with those recorded in the crust of the Khanka massif. The sulphide Os-isotope data show that the subcontinental lithospheric mantle beneath the Khanka massif had formed at least by the Mesoproterozoic, and was subsequently metasomatized by juvenile crustal-growth events related to the evolution of the Altaids. The Khanka massif is further proposed to have tectonic affinity to the Siberia Craton and should originate from it accordingly.
Rosenthal, A., Yaxley, G.M., Crichton, W.A., Kovacs, I.J., Spandler, C., Hermann, J., Sandorne, J.K., Rose-Koga, E., Pelleter, A-A.
Phase relations and melting of nominally 'dry' residual eclogites with variable CaO/Na2O from 3 to 5 Gpa and 1250 to 1500C; implications for refertilisation of upwelling heterogeneous mantle.
Abstract: A classification suggested for alkaline ultramafic rocks of the Ary-Mastakh and Staraya Rechka fields, Northern Anabar Shield, is based on the modal mineralogical composition of the rocks and the chemical compositions of their rock-forming and accessory minerals. Within the framework of this classification, the rocks are indentified as orangeite and alkaline ultramafic lamprophyres: aillikite and damtjernite. To estimate how much contamination with the host rocks has modified their composition when the diatremes were formed, the pyroclastic rocks were studied that abound in xenogenic material (which is rich in SiO2, Al2O3, K2O, Rb, Pb, and occasionally also Ba) at relatively low (La/Yb)PM, (La/Sm)PM, and not as much also (Sm/Zr)PM and (La/Nb)PM ratios. The isotopic composition of the rocks suggests that the very first melt portions were of asthenospheric nature. The distribution of trace elements and REE indicates that one of the leading factors that controlled the diversity of the mineralogical composition of the rocks and the broad variations in their isotopic-geochemical and geochemical characteristics was asthenosphere-lithosphere interaction when the melts of the alkaline ultramafic rocks were derived. The melting processes involved metasomatic vein-hosted assemblages of carbonate and potassic hydrous composition (of the MARID type). The alkaline ultramafic rocks whose geochemistry reflects the contributions of enriched vein assemblages to the lithospheric source material, occur in the northern Anabar Shield closer to the boundary between the Khapchan and Daldyn terranes. The evolution of the aillikite melts during their ascent through the lithospheric mantle could give rise to damtjernite generation and was associated with the separation of a C-H-O fluid phase. Our data allowed us to distinguish the evolutionary episodes of the magma-generating zone during the origin of the Triassic alkaline ultramafic rocks in the northern Anabar Shield.
Abstract: New petrographic, geochemical, and isotopic (Sr, Nd, and ?18?) data on olivine and pyroxene phenocrysts provide constraints on the composition and crustal evolution of primary melts of Paleoproterozoic (2.40 Ga) picrodoleritic sills in the northwest Kola province, Fennoscandian Shield. The picrodolerites form differentiated sills with S-shaped compositional profiles. Their chilled margins comprise porphyritic picrodolerite (upper margin) and olivine gabbronorite (bottom) with olivine and clinopyroxene phenocrysts. Analysis of the available data allows us to recognize three main stages in the crystallization of mineral assemblages. The central parts of large (up to 2 mm) olivine phenocrysts (Ol-1-C) crystallized at the early stage. This olivine (Mg# 85-92) is enriched in Ni (from 2845 to 3419 ppm), has stable Ni/Mg ratio, low Ti, Mn and Co concentrations, and contains tiny (up to 10 ?m) diopside-spinel dendritic lamella that probably originated due to the exsolution from high Ca- and Cr- primary magmatic olivine. All these features of Ol-1-C are typical of olivine from primitive picritic and komatiitic magmas (De Hoog et al., 2010; Asafov et al., 2018). Ol-1-C contains large (up to 0.25 mm) crystalline inclusions of high-Al enstatite (Mg# 80-88) and clinopyroxene (Mg# 82-90), occasionally in association with Ti-pargasite and chromian spinel (60.4 wt.% Al2O3). These inclusions are regarded as microxenoliths of wall rock that were captured by primary melt at depths more than 30 km and preserved due to the conservation in magmatic olivine. The second stage was responsible for the crystallization of Ol-1 rim (Ol-1-R), small (up to 0.3 mm) olivine (Ol-2, Mg# 76-85) grains, and central parts of large (up to 1.5 mm) clinopyroxene (Cpx-C) phenocrysts in the mid-crustal transitional magma chamber (at a depth of 15-20 km) at 1160-1350°C. At the third stage, Cpx-C phenocrysts were overgrown by low-Mg rims (Mg# 70-72) similar in composition to the groundmass clinopyroxene from chilled picrodolerite and gabbro-dolerite in the central parts of the sills. This stage likely completed the evolution of picrodoleritic magma and occurred in the upper crust at a depth of about 5 km. All stages of picrodoleritic magma crystallization were accompanied by contamination. Primary melts were contaminated by upper mantle and/or lower crust as recognized from xenocrystic inclusions in Ol-1-C. The second contamination stage is supported by the negative values of ?Nd(2.40) = -1.1 in clinopyroxene phenocrysts. At the third stage, contamination likely occurred in the upper crust when ascending melts filled gentle fractures. This caused vertical whole-rock Nd heterogeneity in the sills (Erofeeva et al., 2019), and difference in Nd isotopic composition of clinopyroxene phenocrysts and doleritic groundmass. It was also recognized that residual evolved melts are enriched in radiogenic strontium but have neodymium isotopic composition similar to other samples. It could be explained by the interaction of the melts with fluid formed via decomposition of biotite from surrounding gneisses under the effect of high-temperature melts.
Abstract: To provide new insights into the evolution of kimberlitic magmas, we have undertaken a detailed petrographic and mineralogical investigation of highly evolved carbonate-phlogopite-bearing kimberlites of the Kepino cluster, Arkhangelsk kimberlite province, Russia. The Kepino kimberlites are represented by volcanoclastic breccias and massive macrocrystic units within pipes as well as coherent porphyritic kimberlites within sills. The volcanoclastic units from pipes are similar in petrography and mineral composition to archetypal (Group 1) kimberlite, whereas the sills represent evolved kimberlites that exhibit a wide variation in amounts of carbonate and phlogopite. The late-stage evolution of kimberlitic melts involves increasing oxygen fugacity and fluid-phase evolution (forming carbonate segregations by exsolution, etc.). These processes are accompanied by the transformation of primary Al- and Ti-bearing phlogopite toward tetraferriphlogopite and the transition of spinel compositions from magmatic chromite to magnesian ulvöspinel and titanomagnetite. Similar primary kimberlitic melts emplaced as sills and pipes may be transitional to carbonatite melts in the shallow crust. The kimberlitic pipes are characterised by low carbonate amounts that may reflect the fluid degassing process during an explosive emplacement of the pipes. The Kepino kimberlite age, determined as 397.3 ± 1.2 Ma, indicates two episodes of ultramafic alkaline magmatism in the Arkhangelsk province, the first producing non-economic evolved kimberlites of the Kepino cluster and the second producing economic-grade diamondiferous kimberlites.
Abstract: Impact diamonds are technical material with valuable mechanical properties. Despite of a quite long story from their discovery and huge diamond storages at the Popigai astrobleme (Siberia, Russia) they were not involved into industrial production, first of all because of remoteness of objects, complexity of extraction and economically more favourable synthesis of technical diamonds in the seventies of the past century. However, due to the high hardness of impact diamonds and also to the high demand of new carbon materials, including nanomaterials, the interest towards this type of natural diamonds is significantly increased in the recent years. Although the mentioned Popigai astrobleme is situated in a remote part of Russia it has been studied in more details. At the same time, the less known Kara giant meteorite crater (Pay-Khoy, Russia) is situated essentially closer to the industrial infrastructure of the European part of Russia. This astrobleme, similarly to Popigai, is enriched in impact diamonds as well. But, till recent years it was not deeply studied using modern analytical methods. During our studies in 2015 and 2017 at the territory of the Kara meteorite crater we have distinguished and described 5 varieties of impactites - bulk melt impactites which form cover-like and thick dike bodies; melt ultrahigh-pressure vein bodies and at least 3 types of suevites formed after specific sedimentary target rocks. These varieties have typomorphic features regarding the crystallinity and mineral composition. It was found that all of them have high concentration of microdiamonds formed by high-pressure high temperature pyrolysis mechanism from precursor materials like coal and organic relicts. Using a set of modern mineralogical methods we have found two principal types of diamond morphologies within the Kara impactites - sugar-like after coal diamonds and diamond paramorphs after organic relicts. The Kara diamonds have several accompanying carbon substances including newly formed graphite, glass-like carbon and probably carbyne. The studied diamondiferous Kara impactites provide an essentially novel knowledge of impact processes in sedimentary targets.
Abstract: The results of geochemical studies of the diamondiferous suevites of the Kara astrobleme (Pay-Khoy) using a new approach based on “area” microprobe analysis of suevite matrix and consolidated impact melt aggregates with subsequent data processing by multivariate statistic methods are described for the first time. At least three suevite varieties that differ essentially in geomorphology, mineralogy, petrography, and geochemical features have been recognized. The predominant protoliths of the rocks of the target are proposed for these suevite varieties on the basis of integrated data analysis.
Abstract: The variety of morphology and properties of natural diamonds reflects variations in the conditions of their formation in different mantle environments. This study presents new data on the distribution of impurity centers in diamond type Ib-IaA from xenolith of bimineral eclogite from the Udachnaya kimberlite pipe. The high content of non-aggregated nitrogen C defects in the studied diamonds indicates their formation shortly before the stage of transportation to the surface by the kimberlite melt. The observed sectorial heterogeneity of the distribution of C- and A-defects indicates that aggregation of nitrogen in the octahedral sectors occurs faster than in the cuboid sectors.
Journal of Mining Science , Vol. 51, 5, pp. 1235-1241.
Russia
Mineral processing ** in Russian
Abstract: The article presents new test results on structural and chemical properties of mineral formations on the surface of natural hydrophilic diamonds using Raman, X-ray phase and Auger spectroscopy methods. Analysis of morphological features of nano formations involved scanning electron microscope Jeol-5610 and analyzer INCA. Based on the studies into phase composition of diamonds non-recovered in the circuit of kimberlite ore processing, two types of mineral formations are discovered on their surface: microformations as silicate nature globules less than 1 ?m in size and silicate nano films more than 5 nm thick. The tests detect also presence of layered talc silicates that make diamond surface hydrophilic.
Journal of Mining Science, Vol. 52, no. 2, pp. 332-340.
Russia, Yakutia
Deposit - Mir
Abstract: The article gives new experimental data on spectral characteristics of photoluminescence of natural diamonds extracted from deep horizons of Mir and Internatsionalnaya Pipes, Republic of Sakha (Yakutia) depending on composition of basic and additional optically active structural defects in crystals and on temperature during spectrum recording, considering kinetics of luminescence. It is hypothesized on applicability of low-temperature effects to enhance efficiency of photoluminescence separation of diamond crystals.
Journal of Mining Science, Vol. 52, 2, pp. 332-340.
Technology
Spectroscopy
Abstract: The lithosphere beneath the Western Canada Sedimentary Basin has potentially undergone Precambrian subduction and collisional orogenesis, resulting in a complex network of crustal domains. To improve the understanding of its evolutionary history, we combine data from the USArray and three regional networks to invert for P-wave velocities of the upper mantle using finite-frequency tomography. Our model reveals distinct, vertically continuous high (> 1%) velocity perturbations at depths above 200 km beneath the Precambrian Buffalo Head Terrane, Hearne craton and Medicine Hat Block, which sharply contrasts with those beneath the Canadian Rockies ( 1%) at comparable depths. The P velocity increases from ? 0.5% above 70 km depth to 1.5% at 330 km depth beneath southern Alberta, which provides compelling evidence for a deep, structurally complex Hearne craton. In comparison, the lithosphere is substantially thinner beneath the adjacent Buffalo Head Terrane (160 km) and Medicine Hat Block (200 km). These findings are consistent with earlier theories of tectonic assembly in this region, which featured distinct Archean and Proterozoic plate convergences between the Hearne craton and its neighboring domains. The highly variable, bimodally distributed craton thicknesses may also reflect different lithospheric destruction processes beneath the western margin of Laurentia.
Journal of Mining Science, Vol. 52, 3, pp. 535-540.
Russia
Diamond morphology
Abstract: The analytical research has yielded differences in composition of mineral species on the surface of natural diamonds of hyperaltered kimberlites under conditions of diamond ore occurrence and processing. The classification of the mineral species is based on the mineral origin, properties and attachment on the diamond crystal surface.
Journal of Mining Science, Vol. 51, 6, pp. 1235-1241.
Russia
Diamond morphology
Abstract: The article presents new test results on structural and chemical properties of mineral formations on the surface of natural hydrophilic diamonds using Raman, X-ray phase and Auger spectroscopy methods. Analysis of morphological features of nano formations involved scanning electron microscope Jeol-5610 and analyzer INCA. Based on the studies into phase composition of diamonds non-recovered in the circuit of kimberlite ore processing, two types of mineral formations are discovered on their surface: microformations as silicate nature globules less than 1 ?m in size and silicate nano films more than 5 nm thick. The tests detect also presence of layered talc silicates that make diamond surface hydrophilic.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-06174 12p.
Russia, Siberia
deposit - Mirny
Abstract: Here we present new data from a systematic Sr, Nd, O, C isotope and geochemical study of kimberlites of Devonian age Mirny field that are located in the southernmost part of the Siberian diamondiferous province. Major and trace element compositions of the Mirny field kimberlites show a significant compositional variability both between pipes and within one diatreme. They are enriched in incompatible trace elements with La/Yb ratios in the range of (65-00). Initial Nd isotope ratios calculated back to the time of the Mirny field kimberlite emplacement (t?=?360 ma) are depleted relative to the chondritic uniform reservoir (CHUR) model being 4 up to 6 ?Nd(t) units, suggesting an asthenospheric source for incompatible elements in kimberlites. Initial Sr isotope ratios are significantly variable, being in the range 0.70387-0.70845, indicating a complex source history and a strong influence of post-magmatic alteration. Four samples have almost identical initial Nd and Sr isotope compositions that are similar to the prevalent mantle (PREMA) reservoir. We propose that the source of the proto-kimberlite melt of the Mirny field kimberlites is the same as that for the majority of ocean island basalts (OIB). The source of the Mirny field kimberlites must possess three main features: It should be enriched with incompatible elements, be depleted in the major elements (Si, Al, Fe and Ti) and heavy rare earth elements (REE) and it should retain the asthenospheric Nd isotope composition. A two-stage model of kimberlite melt formation can fulfil those requirements. The intrusion of small bodies of this proto-kimberlite melt into lithospheric mantle forms a veined heterogeneously enriched source through fractional crystallization and metasomatism of adjacent peridotites. Re-melting of this source shortly after it was metasomatically enriched produced the kimberlite melt. The chemistry, mineralogy and diamond grade of each particular kimberlite are strongly dependent on the character of the heterogeneous source part from which they melted and ascended.
Journal of Mineral Science, Vol. 54, 3, pp. 458-465.
Russia
luminescence
Abstract: Organic and inorganic luminophores of similar luminescence parameters as diamonds are selected. Indicators, based on the selected luminophores, are synthesized. Spectral and kinetic characteristics of luminophores are experimentally determined for making a decision on optimal compositions to ensure maximum extraction of diamonds in X-ray luminescence separation owing to extra recovery of non-luminescent diamond crystals. As the components of luminophore-bearing indicators, anthracene and K-35 luminophores are selected as their parameters conform luminescence parameters of diamonds detected using X-ray luminescence separator with standard settings.
Journal of Mining Science, Vol. 56, 1, pp. 96-103. pdf
Global
luminescence
Abstract: The authors present an efficient modification method of X-ray fluorescence separation with mineral and organic luminophores used to adjust spectral and kinetic characteristics of anomalously luminescent diamonds. The mechanism of attachment of luminophores at diamonds and hydrophobic minerals is proved, including interaction between the organic component of emulsions and the hydrophobic surface of a treated object and the concentration of insoluble luminophore grains at the organic and water interface. Selective attachment of the luminophore-bearing organic phase of emulsion at the diamond surface is achieved owing to phosphatic dispersing agents. Tri-sodium phosphate and sodium hexametaphosphate added to emulsion reduce attachment of the luminophore-bearing organic phase at the surface of kimberlite minerals. It is shown that phosphate concentration of 1.0-1.5 g/l modifies and stabilizes spectral and kinematic parameters of kimberlite mineral on the level of initial values. This mode maintains the spectral and kinematic characteristics of anomalously luminescent diamonds at the wanted level to ensure extraction of diamonds to concentrate.
Journal of Mining Science, Vol. 56, 1, pp. 96-103, 8p. Pdf
Russia
luminescence
Abstract: The authors present an efficient modification method of X-ray fluorescence separation with mineral and organic luminophores used to adjust spectral and kinetic characteristics of anomalously luminescent diamonds. The mechanism of attachment of luminophores at diamonds and hydrophobic minerals is proved, including interaction between the organic component of emulsions and the hydrophobic surface of a treated object and the concentration of insoluble luminophore grains at the organic and water interface. Selective attachment of the luminophore-bearing organic phase of emulsion at the diamond surface is achieved owing to phosphatic dispersing agents. Tri-sodium phosphate and sodium hexametaphosphate added to emulsion reduce attachment of the luminophore-bearing organic phase at the surface of kimberlite minerals. It is shown that phosphate concentration of 1.0-1.5 g/l modifies and stabilizes spectral and kinematic parameters of kimberlite mineral on the level of initial values. This mode maintains the spectral and kinematic characteristics of anomalously luminescent diamonds at the wanted level to ensure extraction of diamonds to concentrate.
Doklady Earth Sciences, Vol. 471, 2, pp. 1303-1306.
Technology
Diamond crystallography
Abstract: The occurrence rates of combinatorial types of simple polyhedra {111} are analyzed for natural and artificial diamonds. The empirical occurrence rates of 14 possible polyhedra in an isotropic environment are obtained based on numeral simulation of growth forms of octahedral crystals by the Monte-Carlo method. The phenomenon of dissymmetrization by Curie’s principle related to the crystallization conditions is established for artificial and natural diamonds.
Chemical composition, volatile components, and trace elements in the magmatic melt of the Kurama mining district, middle Tien Shan: evidence investigation of quartz inclusions
Vladykin, N.V., Deep Seated Magmatism: its sources and plumes, pp. 75-92.
Mertanen, S., Vuollo, J.I., Huhma, H., Arestova, N.A., Kovalenko, A.
Early Paleoproterozoic Archean dykes and gneisses in Russian Karelia of the Fennoscandian Shield - new paleomagnetic, isotope age, geochemical investigations.
Precambrian Research, Vol. 144, 3-4, Feb. 10, pp. 239-260.
Journal of Mining Science, Vol. 57, 2, pp. 286-297. pdf
Russia
IPKON RAS
Abstract: The thermodynamic analysis and tests of minerogenesis under higher temperatures determine conditions of thermochemical decomposition of hydrophilic attachments on diamond surface. It is found that hydrophilic mineral attachments can be removed from diamond surface by combining thermal treatment of slurry at the temperature of 80-85 ?C with electrochemical treatment of recirculated water, which enables required change in ion-molecule composition of water phase in the slurry. The hybrid conditioning technology ensures recovery of the natural hydrophobic behavior and floatability of diamonds and enhances performance of froth flotation of diamonds by 5.1%.
Abstract: An unusual variety of impact-related diamond from the Popigai impact structure - yakutites - is characterized by complementary methods including optical microscopy, X-ray diffraction, radiography and tomography, infra-red, Raman and luminescence spectroscopy providing structural information at widely different scales. It is shown that relatively large graphite aggregates may be transformed to diamond with preservation of many morphological features. Spectroscopic and X-ray diffraction data indicate that the yakutite matrix represents bulk nanocrystalline diamond. For the first time, features of two-phonon infra-red absorption spectra of bulk nanocrystalline diamond are interpreted in the framework of phonon dispersion curves. Luminescence spectra of yakutite are dominated by dislocation-related defects. Optical microscopy supported by X-ray diffraction reveals the presence of single crystal diamonds with sizes of up to several tens of microns embedded into nanodiamond matrix. The presence of single crystal grains in impact diamond may be explained by CVD-like growth in a transient cavity and/or a seconds-long compression stage of the impact process due to slow pressure release in a volatile-rich target. For the first time, protogenetic mineral inclusions in yakutites represented by mixed monoclinic and tetragonal ZrO2 are observed. This implies the presence of baddeleyite in target rocks responsible for yakutite formation.
Journal of Crystal Growth, Vol. 550, 12890, 6p. Pdf
Global
synthetics
Abstract: The morphology of ultra-large polyhedra of diamond grown under high pressure and high temperature (5.6-5.8 GPa and 1400-1700 °C) in a growth system based on Fe-Co was studied. The grown diamond polyhedra are crystals of an octahedral habit with minor faces of a cube, rhombic dodecahedron, and trapezohedrons {3 1 1}, {5 1 1} and {7 1 1}. The morphological features of the grown crystals are the skeletal growth of faces of various simple forms and the so-called "binary growth" of single crystal. The characteristic of these growth phenomena is given and possible reasons for their manifestation are described.
Trace elements and volatile components in silicate and silicate salt magmas of the Mushugai Khuduk carbonatite bearing alkaline complex, southern Mongolia.
International Mineralogical Association meeting August Budapest, abstract p. 564.
Kovalenko, V.I., Solovova, I.P., Ryabchikov, I.D., et al.
Fluidized CO2 sulphide silicate media as agents of mantle metasomatism and megacrysts formation: evidence from a large druse in a spinel lherzolitexenolith
Physics of the Earth and Planetary Interiors, Vol. 45, No.3 April pp. 280-293
Magma compositions and genesis of the rocks of the Mushugai Khuduk carbonatite bearing alkalic complex ( southern Mongolia): evidence from melt inclusions.
Periodico di Mineralogia, (in english), Vol. LXX11, 1. April, pp. 95-105.
Late Riphean rifting and breakup of Laurasia: dat a on geochronological studies of ultramafic alkaline complexes in the southern framing of the Siberian Craton.
Doklady Earth Sciences, Vol. 404, 7, pp. 1031-1036.
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.
Modern volcanism in the Earth's northern hemisphere and its relation with the evolution of the North Pangaea modern supercontinent and with the spatial ... hotspots
Abstract: The first data on the discovery of Th-Sc mineralization in the pyritic complexes of the Southern Urals are presented. The minerals of Th (thorite) and Sc-containing thorium minerals are described. The conclusion is made that the Th-Sc mineralization formed due to crystallization of a residual melt in the local volume.
Abstract: The first data on the discovery of Th-Sc mineralization in the pyritic complexes of the Southern Urals are presented. The minerals of Th (thorite) and Sc-containing thorium minerals are described. The conclusion is made that the Th-Sc mineralization formed due to crystallization of a residual melt in the local volume.
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.
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.
Journal of the Belarusian State University. Geography and Geology, Title only
Russia
deposit - Vitebsk
Abstract: The article describes the history of studying the diamond content of tectonic structures of the territory of Belarus. Based on the results of magnetometric, mineralogical, tectonic studies carried out by industrial geologists and scientists over the past 50 years, new scientifically substantiated criteria for the search for explosion pipes have been developed using Clifford’s rule, according to which kimberlite explosion pipes are developed within the Archean cratons, where the thickness of the lithosphere is 175–270 km, and are absent in the zones of Early Proterozoic stabilisation and tectonomagmatic activation. Explosion tubes on the African-Arabian, East Siberian, Sino-Korean and East European platforms demonstrate their confinement to the Archean cratons and may be associated with zones of paleosubduction of the Proterozoic oceanic crust beneath the Archean cratons. Based on this, the authors scientifically substantiated the hypothesis that during the closure of the Early Proterozoic paleoocean separating the Fenno-Scandinavian craton from the Volga-Ural and Sarmatian cratons, subduction of the younger crust took place under these cratons, the southwestern corner of which on the territory of Belarus is the Vitebsk granulite massif. The article concludes that the Vitebsk granulite massif is the most promising in terms of diamond-bearing on the territory of Belarus, and within its limits – the Smolensk regional deep fault at the intersection of this fault of northeastern striking with the Odessa-Gomel regional deep fault of submeridional striking south of the city of Orsha. Recommendations are given for further study of promising areas in order to determine their diamond content.
Paragenesis and origin of olivine macrocrysts from Udachnaya-East hypabyssal kimberlite, Yakutia, Russia.
V.S. Sobolev Institute of Geology and Mineralogy Siberian Branch Russian Academy of Sciences International Symposium Advances in high pressure research: breaking scales and horizons ( Courtesy of N. Poikilenko), Held Sept. 22-26, 2p. Abstract
Paragenesis and complex zoning of olivine macrocrysts from unaltered kimberlite of the Udachnaya-East pipe, Yakutia: relationship with the kimberlite formation conditions and evolution.
Russian Geology and Geophysics, Vol. 56, 1, pp. 260-279.
Abstract: Isotopic and trace element variations within single diamond crystals are widely known from both natural stones and synthetic crystals. A number of processes can produce variations in carbon isotope composition and nitrogen abundance in the course of diamond crystallization. Here, we present evidence of carbon and nitrogen fractionation related to the growing surfaces of a diamond. We document that difference in the carbon isotope composition between cubic and octahedral growth sectors is solvent-dependent and varies from 0.7‰ in a carbonate system to 0.4‰ in a metal-carbon system. Ab initio calculations suggest up to 4‰ instantaneous 13C depletion of cubic faces in comparison to octahedral faces when grown simultaneously. Cubic growth sectors always have lower nitrogen abundance in comparison to octahedral sectors within synthetic diamond crystals in both carbonate and metal-carbon systems. The stability of any particular growth faces of a diamond crystal depends upon the degree of carbon association in the solution. Octahedron is the dominant form in a high-associated solution while the cube is the dominant form in a low-associated solution. Fine-scale data from natural crystals potentially can provide information on the form of carbon, which was present in the growth media.
Abstract: Isotopic and trace element variations within single diamond crystals are widely known from both natural stones and synthetic crystals. A number of processes can produce variations in carbon isotope composition and nitrogen abundance in the course of diamond crystallization. Here, we present evidence of carbon and nitrogen fractionation related to the growing surfaces of a diamond. We document that difference in the carbon isotope composition between cubic and octahedral growth sectors is solvent-dependent and varies from 0.7h in a carbonate system to 0.4h in a metal-carbon system. Ab initio calculations suggest up to 4h instantaneous 13C depletion of cubic faces in comparison to octahedral faces when grown simultaneously. Cubic growth sectors always have lower nitrogen abundance in comparison to octahedral sectors within synthetic diamond crystals in both carbonate and metal-carbon systems. The stability of any particular growth faces of a diamond crystal depends upon the degree of carbon association in the solution. Octahedron is the dominant form in a high-associated solution while the cube is the dominant form in a low-associated solution. Fine-scale data from natural crystals potentially can provide information on the form of carbon, which was present in the growth media.
Stability and compressibility of the high pressure phases of AL203 up to 200 GPa: implications for the electrical conductivity of the base of the lower mantle.
Earth and Planetary Science Letters, Vol. 246, 3-4, pp. 326-335.
Skeleton, A., Whitmarsh, R., Arghe, F., Crill, P., Koyi, H.
Constraining the rate and extent of mantle serpentinization from seismic and petrological data: implications for chemosynthesis and tectonic processes.
Skelton, A., Whitmarsh, R., Arghe, F., Crill, P., Koyi, H.
Constraining the rate and extent of mantle serpentinization from seismic and petrological data: implications for chemosynthesis and tectonic processes.
Abstract: We have investigated a diamond crystal that consists of several misorientated subgrains. The main feature of the crystal is the dark in the cathodoluminescence core that has “estuary-like” boundaries extending along the subgrain interfaces. The core has more than 3100 ppm of nitrogen, and the share of the B form is more than 95%; the absorbance of the centre N3VH at 3107 cm -1 reaches 75 cm-1. The N3 centre’s absorbance, as well as N3 luminescence, is absent in the core. In the outer part of the crystal, the bright blue luminescence of the N3 centre is registered, and the N3 absorbance reaches 5.3 cm-1. These observations may be explained by the conversion of N3 centres to N3VH after attaching a hydrogen atom. After the full conversion of the N3 centres, the diamond becomes darker under CL. We hypothesize the dark core has a specific shape due to the post-growth diffusion of the hydrogen.
Abstract: A wide range of model temperature, which is typical for dodecahedroids from placer deposits in the Urals, Brazil, and the northern Yakutia diamond province has been identified in diamond crystals of the Ichetyu Ural-type diamonds deposit, Central Urals. Plates were cut from six crystals; it have been studied with cathodoluminescence and infrared and photoluminescence spectroscopy. Octahedral zoning predominates in the internal structure of rounded dodecahedroids, and growth layers are cut by the surface. Surface pigmentation spots are exhibited in the cathodoluminescent images of all plates. The nitrogen concentration in Ichetyu diamonds ranges from 100 to 2200 ppm and its proportion as B1 defects varies from 0 to 100%. The maximum absorption coefficient of hydrogen band is 56 cm-1 with an average value of 0.8 cm-1.
Journal of Mining Institute * not sure if in english?, Vol. 239, 5, pp. 492-496.
Russia
diamond crystallography
Abstract: The article presents the results of a study of the internal structure of highly elongated diamond crystals from placers in the Krasnovishersky district of the Urals. Very elongated crystals are found within diamond-bearing placer with unrevealed primary sources. Determining the conditions of such crystals formation can help one to determine the primary deposits type. There are three hypotheses for the formation of the elongated shape of such crystals: 1) crystals initially elongated along the <100> (strongly distorted octahedra); 2) individual crystals of columnar aggregates; 3) elongated crystals fragments. To study the internal structure, we selected three most elongated individuals of the 155 crystals samples. The study of the internal structure of selected crystals with the usage of photoluminescent (PL) tomography, cathodoluminescence (CL), and optical microscopy has shown that these samples are fragments of larger single crystals. CL imaging allowed to determine slip lines within the crystal's volume. The recorded PL spectra show the 912, 946, and 986 nm peaks, which are characteristic of crystals with plastic deformation. The revealed features are indicators of plastic deformation accompanying the destruction of the crystals. The significant dissolution following the destruction of the crystals led to the rounding of the vertices and edges of their fragments. Apparently, most of the very elongated crystals from placers with unknown sources are also highly dissolved isometric crystal fragments. The obtained results have shown that the deformation and dissolution of diamond crystals are related events characteristic of diamonds from hitherto undetected, but highly productive primary deposits.
Abstract: We have performed an analysis of the cases of synchronism in th egrowth temperature in local zones of diamond crystals and the concentration of hydrogen in them.The considered cases were observed by the authors and fined out in the iterature. Possible causes of the simbatic change in the crystal growth temperature and the concentration of hydrogen in it are considered.The determination of the temperature change over the zones was carried out on the basis of local FTIR spectroscopy from the ratio of the nitrogen concentration in the form of defects in the crystal structure of A and B1, and size the B2 defects.The change in the hydrogen concentration in various zones of diamond crystals was estimated from the 3107cm-1 band of the hydrogen-containing defect. It is shown that in the analyzed cases the concentration of hydrogen in diamond is determined mainly by its content in the growth medium.We accept the obtained results as evidence of the participation of hydrogen in the heat transfer in mantle mineral-forming systems.
Abstract: The Vuoriyarvi Devonian alkaline-ultramafic complex (northwest Russia) contains magnesiocarbonatites with rare earth mineralization localized in the Petyayan-Vara area. High concentrations of rare earth elements are found in two types of these rocks: (a) ancylite-dominant magnesiocarbonatites with ancylite-baryte-strontianite-calcite-quartz (±late Ca-Fe-Mg carbonates) ore assemblage, i.e., “ancylite ores”; (b) breccias of magnesiocarbonatites with a quartz-bastnäsite matrix (±late Ca-Fe-Mg carbonates), i.e., “bastnäsite ores.” We studied fluid inclusions in quartz and late-stage Ca-Fe-Mg carbonates from these ore assemblages. Fluid inclusion data show that ore-related mineralization was formed in several stages. We propose the following TX evolution scheme for ore-related processes: (1) the formation of ancylite ores began under the influence of highly concentrated (>50 wt.%) sulphate fluids (with thenardite and anhydrite predominant in the daughter phases of inclusions) at a temperature above300-350 °C; (2) the completion of the formation of ancylite ores and their auto-metasomatic alteration occurred under the influence of concentrated (40-45 wt.%) carbonate fluids (shortite and synchysite-Ce in fluid inclusions) at a temperature above 250-275 °C; (3) bastnäsite ores deposited from low-concentrated (20-30 wt.%) hydrocarbonate-chloride fluids (halite, nahcolite, and/or gaylussite in fluid inclusions) at a temperature of 190-250 °C or higher. Later hydrothermal mineralization was related to the low-concentration hydrocarbonate-chloride fluids (<15 wt.% NaCl-equ.) at 150-200 °C. The presented data show the specific features of the mineral and fluid evolution of ore-related late-stage hydrothermal rare earth element (REE) mineralization of the Vuoriyarvi alkaline-ultramafic complex.
Abstract: This article is devoted to the geology of titanium-rich varieties of the Petyayan-Vara rare-earth dolomitic carbonatites in Vuoriyarvi, Northwest Russia. Analogues of these varieties are present in many carbonatite complexes. The aim of this study was to investigate the behavior of high field strength elements during the late stages of carbonatite formation. We conducted a multilateral study of titanium- and niobium-bearing minerals, including a petrographic study, Raman spectroscopy, microprobe determination of chemical composition, and electron backscatter diffraction. Three TiO2-polymorphs (anatase, brookite and rutile) and three pyrochlore group members (hydroxycalcio-, fluorcalcio-, and kenoplumbopyrochlore) were found to coexist in the studied rocks. The formation of these minerals occurred in several stages. First, Nb-poor Ti-oxides were formed in the fluid-permeable zones. The overprinting of this assemblage by residual fluids led to the generation of Nb-rich brookite (the main niobium concentrator in the Petyayan-Vara) and minerals of the pyrochlore group. This process also caused niobium enrichment with of early generations of Ti oxides. Our results indicate abrupt changes in the physicochemical parameters at the late hydro (carbo) thermal stage of the carbonatite formation and high migration capacity of Ti and Nb under these conditions. The metasomatism was accompanied by the separation of these elements.
Abstract: A study of radiogenic (Sr, Nd) and stable (C, O) isotopic data for rare earth carbonatites from the Petyayan-Vara field of the Devonian Vuoriyarvi alkaline-ultrabasic massif is presented. The cumulative evidence indicates that the primary igneous rocks of the Petyayan-Vara area are burbankite-bearing magnesiocarbonatites having isotopic signatures of the depleted mantle (?Nd365Ma = 5.0, 87Sr/86Sr(i) = 0.7031, ?13C ca. -4‰, and ?18O ca. 11‰). Interaction of the primary carbonatite melt with the host silicate rocks produced high-Ti carbonatites with a mantle ?13C (ca. -4‰) and isotopically heavy ?18O (ca. 20‰). These rocks trapped K, Na, Mg, CO2, and rare earth elements (REEs) (mainly heavy REEs) from the melt and Si, Al, Fe, Ti, and P from the host rocks. Early post-magmatic exposure of burbankite-bearing carbonatites to a mixture of fluids of crustal and orthomagmatic carbonatite origin caused redistribution of REEs, Ba, and Sr and formation of REE-rich carbonatites with abundant ancylite mineralization. This effect did not disturb the Smsingle bondNd system but induced radiogenic Sr accumulation and a change in C and O isotopic composition towards heavier values. Later, but most likely before denudation, the Petyayan-Vara rocks underwent another metasomatic event involving crustal fluids infiltrating through fracture systems. This event triggered formation of bastnäsite-rich carbonatites with fewer REEs at the expense of ancylite-rich carbonatites, and changed all the isotopic systems in the affected rocks. This model successfully accounts for the evolution of all the carbonatite varieties discovered to date in the Petyayan-Vara field.
Abstract: On the basis of quantum-chemical calculations of the linear to isomeric bent transition of the SiO2 molecule, it is suggested that the bent to linear transition of SiO2 forms can occur in melted mantle minerals of the lower mantle. This may be important for the formation of the peculiarities of mantle convection and origination of plumes.
Crust mantle boundary in the central Fennoscandian shield: constraints from wide angle P and S wave velocity models and new results of reflection profiling in Finland
Journal of Geophysical Research, Vol. 112, B4, B04302.
Janik, T., Kozlovskaya, E., Helikkinen, P., Tliniemi, J.
Evidence for preservation of crustal root beneath the Proterozoic Lapland-Kola orogen ( northern Fennoscandian shield) derived from P and S wave models.
Journal of Geophysical Research, Vol. 114. B 6, B06308.
Abstract: The role of magmatic differentiation is considered for the formation of the Ulan-Tologoi Ta-Nb-Zr deposit (northwestern Mongolia) related to the eponymous alkali granite pluton. Data are presented on the structure of the pluton, the composition of its rocks, and distribution of rare metal mineralization. The ores of the pluton include alkali granites with contents of ore elements exceeding the normative threshold for Ta (>100 ppm). The rare metal mineralization includes pyrochlore, columbite, zircon, bastnaesite, monazite, and thorite, which are typical of all alkali-salic rocks; however, their amount varies depending on the REE content of the rocks. The pluton was formed ~298 Ma ago under the influence of a mantle-crustal melt source.
Abstract: International Symposium on Deep Earth Exploration and Practices Beijing, China -October24-26, 2018The protolithnatureof diamondiferous metamorphic rocks of the Kokchetav MassifVladislav Shatsky1,2,3, Emil Jagoutz4, Olga Kozmenko1, Alexey Ragozin1,3, Sergei Skuzovatov2and Nikolai Sobolev1,31Sobolev Institute of Geology and Mineralogy SB RAS, Novosibirsk, 630090, Russia, [email protected] Institute of Geochemistry SB RAS, Irkutsk, Russia3Novosibirsk State University, Novosibirsk, Russia4Max Planck Institute for Chemistry, Mainz, GermanyUltra-high-pressure diamondiferous rocks (UHP) of the Kokchetav subduction-collision zone are considered as an idealobject for studying the mobility of elements insubduction zones of the continental type. The compositional diversity of metasedimentary rocks subjected to UHP metamorphism makes it difficult to establish the nature of their protoliths. This, in turn, complicates estimatesof the degree of depletionof the UHP metamorphic rocks relative to the protoliths.To clarify the nature of protholiths of the Kokchetav diamondiferous rocks we studied the geochemical features and Sm-Nd isotopic composition of diamondiferous calc-silicate, garnet-pyroxene rocks, high-alumina metapelitesand barren granite-gneisses.The nine samples of the Kumdy Kol mocrodiamond deposit (one granite-gneiss, 4-calc-silicate rocks, 3-garnet-pyroxenite) yielded aSm-Nd whole-rockisochronageof 1052±44 Ma. This age is close to the age of formation of the granitic gneiss basement of the Kokchetav massif (1.2-1.05 Ga) (Glorie et al., 2015). Therefore, we assume that the protoliths of these rocks were basementrocks. In this interpretation, their geochemical features may not be directly related to the processes of ultrahigh-pressure metamorphism.At the same time, the high-alumina rocks of the Barchinsky area are depleted todifferent degreeswithrespect to LREE and K yieldeda whole-rockisochron with an age of 509 ± 32 Ma, which suggests partial melting of these rocks duringthe exhumation stage.It was previously assumed that metasedimentary rocks of the Kokchetav microcontinent are the protoliths of diamondiferous rocks (Buslov et al., 2015). However, this contradicts with Sm-Nd isotopic data for metasedimentary rocks of quartzite-schist sequences of the Kokchetav microcontinent (Kovach et al., 2017). The metasedimentary rocks of the Sharyk Formation are characterized by variations in the ?Nd(t)from +4.1 to -3.3 and intNd(DM)from 1.9 to 1.25 Ga, whereasin the UHP metamorphic rocks ?Nd(t)varies from -7.6 to -13.2, and the model ages range from 2.7 to 2.3 Ga. These data clearly indicate that the metasedimentary rocks of the Kokchetav massif could not be the protolith of the ultrahigh-pressure rocks.
Abstract: The results of the first study of the PGE distribution in deformed lherzolites of the Udachnaya kimberlite pipe (Yakutia) are presented here. The complex character of evolution of the PGE composition in the Deformed lherzolites is assumed to be the result of silicate metasomatism. At the first stage, growth in the amount of clinopyroxene and garnet in the rock is accompanied by a decrease in the concentration of the compatible PGE (Os, Ir). During the final stage, the rock is enriched with incompatible PGE (Pt, Pd) and Re possible due to precipitation of submicron-sized particles of sulfides in the interstitial space of these mantle rocks.
Doklady Earth Sciences, Vol. 493, 1, pp. 513-516. pdf
Russia, Yakutia
subduction
Abstract: The data available indicate the complex evolution of deformed peridotites of mantle xenoliths, the P-T parameters of which indicate that they are fragments of the metasomatized lower part of the cratonic lithosphere. The zoning established in garnets from xenoliths in kimberlite pipes is interpreted as a result of metasomatism that occurred shortly before xenoliths reached the surface. Metasomatic alterations in xenoliths of deformed harzburgites were manifested not only in the development of zoning of minerals. The study results show that there is a discrepancy between the data calculated based on the contents of incompatible elements in minerals of xenoliths and those obtained due to direct measurements of the bulk composition of xenoliths. To determine the balance of incompatible elements, we have carried out experiments on leaching xenoliths of deformed lherzolites from the Udachnaya kimberlite pipe. It was established that a significant part of LREEs in the studied xenoliths occurs in the intergranular space. The distribution pattern of incompatible elements and, in particular, the presence of a positive Eu anomaly indicate that the appearance of the intergranular component is not associated with contamination of xenoliths by the kimberlite melt. Quite a few xenoliths demonstrate a positive Eu anomaly, which indicates the influence of the subducted crustal component at one of the modification stages of xenoliths.
Russian Geology and Geophysics, Vol. 62, pp. 547-556, pdf
Russia, Kazakhstan
deposit - Kokchetav
Abstract: The isotope-geochemical features of diamondiferous metamorphic rocks of the Kokchetav subduction–collision zone (KSCZ) show that both the basement rocks and the sediments of the Kokchetav massif were their protoliths. A whole-rock Sm–Nd isochron from the diamondiferous calc-silicate, garnet–pyroxene rocks and migmatized granite-gneisses of the western block of the KSCZ yielded an age of 1116 ± 14 Ma, while an age of 1.2–1.1 Ga was obtained by U–Pb dating of zircons from the granite-gneiss basement of the Kokchetav microcontinent. Based on these data, we assume that the protoliths of the calc-silicate, garnet–pyroxene rocks and the granite-gneisses of the KSCZ were the basement rocks sharing an initially single Nd source, which was not influenced by high- to ultrahigh-pressure metamorphism (~530 Ma). Therefore, their geochemical features are probably not directly related to ultrahigh-pressure metamorphism. The corresponding rock associations lack isotope-geochemical evidence of partial melting that would occur during ultrahigh-pressure metamorphism, which suggesting that they were metamorphosed under granulite-facies conditions. At the same time, the high-alumina diamondiferous rocks of the Barchi area (garnet–kyanite–mica schists and granofelses), which were depleted to different degrees in light rare-earth elements (REE) and K, have yielded a Sm–Nd whole-rock isochron age of 507 ± 10 Ma indicating partial melting of these rocks during their exhumation stage. The close ?Nd (1100) values of the basement rocks and garnet–kyanite–mica schist with geochemical characteristics arguing against its depletion during high-pressure metamorphism indicate that the basement rocks were a crustal source for high-alumina sediments.
Journal of Asian Earth Sciences, Vol. 188, 26p. Pdf
Russia, Siberia
carbonatite
Abstract: The Cambrian Kharly alkaline plutonic complex composed mainly of foidolite and nepheline syenite makes up a small intrusive field in the Sangilen Plateau in Tuva (southern Siberia). The rocks show large ranges of major oxides (38-58 wt% SiO2; 1-18 wt% Na2O + K2O; 11-28 wt% Al2O3; 1.5-20 wt% CaO; 0.1-8 wt% MgO; 2-12 wt% Fe2O3) controlled by variable percentages of minerals: clinopyroxenes, calcic amphiboles, micas, nepheline and feldspars. Alkaline rocks are cut by carbonatite veins composed of predominant calcite coexisting with femic minerals (10-15% of aegirine-ferrosalite-hedenbergite, sodic-calcic amphiboles, ferrobiotite, Ti-garnet), Na-K feldspar and nepheline (up to 15-20%), fluorapatite (up to 20-25%), Sr-apatite, and accessory carbocernaite, titanite, Ti-magnetite and ilmenite. Carbonatites (4057-8859 ppm Sr, 426-1901 ppm Ba (Sr/Ba ? 2), 290-980 ppm REE + Y, 2 to 100 ppm Zr, and 0.5 to 15 ppm Nb) possibly originated at high (?500-650 °C) temperatures as a result of liquid immiscibility. The isotope systematics of rocks and minerals (?Nd(t) from ~2.9 to 6.5; 207Pb/206Pbin = 0.89; 208Pb/206Pbin = 2.15; 87Sr/86Sr(t) = 0.70567-0.70733, ?18OV-SMOW ? 7.2-19.5‰, and ?13CV-PDB from ?6.0 to ?1.4‰) suggest mixing of PREMA and EM 1 material during magma generation and crustal contamination of the evolving melts. The rocks bear signatures of interaction with “magmatic-equilibrated” fluids or heated meteoric waters. LILE/HFSE ratios indicate mixed magma sources that involved the material of IAB and OIB, as well as a crustal component, possibly, due to interaction of a mantle plume with rock complexes on the active continental margin.
Abstract: The paper discusses questions related to the generation of increasing crustal horizontal compressive stresses compared to the idea of the standard gravitational state at the elastic stage or even from the prevalence of horizontal compression over vertical stress equal to the lithostatic pressure. We consider a variant of superfluous horizontal compression related to internal lithospheric processes occurrin in the crust of orogens, shields, and plates. The vertical ascending movements caused by these motions at the sole of the crust or the lithosphere pertain to these and the concomitant exogenic processes giving rise to denudation and, in particular, to erosion of the surfaces of forming rises. The residual stresses of the gravitational stressed state at the upper crust of the Kola Peninsula have been estimated for the first time. These calculations are based on the volume of sediments that have been deposited in Arctic seas beginning from the Mesozoic. The data speak to the possible level of residual horizontal compressive stresses up to 90 MPa in near-surface crustal units. This estimate is consistent with the results of in situ measurements that have been carried out at the Mining Institute of the Kola Science Center, Russian Academy of Sciences (RAS), for over 40 years. It is possible to forecast the horizontal stress gradient based on depth using our concept on the genesis of horizontal overpressure, and this forecasting is important for studying the formation of endogenic deposits.