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SDLRC - Scientific Articles all years by Author - Z
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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Abstract: Water transported by deep subduction to the mantle transition zone (MTZ) that is eventually released and migrates upwards is invoked as a likely cause for hydroweakening and cratonic lithosphere destruction. The destruction of the North China Craton (NCC) during the Mesozoic has been proposed to be related to hydroweakening. However, the source of water related to large-scale craton destruction in the NCC is poorly constrained. Some suggest that the water was mainly released from a flat-lying (or stagnating) slab in the MTZ, whereas others posit that most water was released from a previously existing strongly hydrous MTZ then perturbed by the stagnating subduction in the MTZ layer. In this study, we use numerical modeling to evaluate the water carrying ability of flat-lying slabs in the MTZ with different slab ages and water contents to simulate its maximum value and discuss its potential role on large-scale hydroweakening and craton destruction. Our results reveal that a single flat-lying slab in the MTZ cannot provide enough water for large-scale cratonic lithosphere hydroweakening and thinning. Water estimates invoked for craton destruction as experienced by the NCC can only be the result of long-term piling of multiple slabs in the MTZ or penetrating deeper into the lower mantle.
Zirconolite and Zr Th U minerals in chromities of the Finero complex, western Alps, Italy: evidence for carbonatite type metasomatism in a subcontinental ... mantle plume.
Abstract: Empirical and experimental calibration of single element solubility thermometers, such as Zr-in-rutile, Zr-in-titanite, Ti-in-zircon, and Ti-in-quartz, within the past 13 years has greatly expanded our ability to assess the pressure and temperature conditions of individual minerals associated with specific textures in metamorphic rocks. Combined with advances in in situ techniques for analyzing trace concentrations, this has led to an increase in the combined use of single element thermometers, geochronometers, and isotope ratios, often simultaneously, in metamorphic minerals. Here we review the calibration and application of single element thermometers at the pressure and temperature conditions of interest in metamorphic rocks. We discuss to what extent accessory phase equilibrium and trace element equilibrium are attained in metamorphic systems, and the thermodynamic and kinetic framework within which trace element equilibrium is assessed. As an example, we present a comprehensive study of trace element distribution during rutile replacement by titanite in rocks that experienced high-temperature amphibolite-facies overprinting and those that underwent low-temperature blueschist-facies overprinting from a variety of subduction-related terranes worldwide. We find that trace element distributions approach equilibrium partition coefficients in rocks from amphibolite-facies overprinted terranes, whereas trace element distributions do not approach equilibrium in rocks that experienced blueschist-facies overprinting. We caution that single element thermometers that rely upon slow-diffusing high field strength elements should not be applied to rocks equilibrated at <600 °C unless attainment of trace element equilibrium can be demonstrated.
Abstract: Rare-earth elements play a crucial role in modern technologies and are necessary for a transition to a green economy. Potentially economic deposits of these elements are typically hosted in minerals such as monazite, bastnäsite, and eudialyte (a complex Na-Ca-Fe-Zr silicate mineral with Cl), making these prime targets for geological research. Globally, rare-earth mineral deposits commonly show evidence of polyphase development and mineralisation processes, which need to be better understood to improve exploration strategies. The Norra Kärr alkaline complex (Sweden) contains a globally significant deposit of rare-earth elements, hosted in the mineral eudialyte. In this study, we focussed on eudialyte crystals in undeformed, cross-cutting pegmatoid veins from Norra Kärr. In order to determine their age, we refined an established micromilling method to enable sampling of minerals rich in rare-earth elements for precise analysis of major and trace elements, Nd isotope ratios, and Sm-Nd geochronology down to a scale of <200?µm. Mineral samples were subjected to detailed textural and chemical characterisation by backscattered electron imaging and laser ablation inductively coupled plasma mass spectrometry, by which precise and accurate Sm/Nd ratios were determined to steer subsequent micromill sampling for small-aliquot Sm-Nd isotope analysis by isotope dilution thermal ionisation mass spectrometry. Given enough internal spread in Sm/Nd ratios, reliable Sm-Nd isochrons can be derived from discrete textural domains within a single crystal. This provided an age of 1.144?±?0.053?Ga (95% confidence); approximately 350?million?years younger than the magmatic intrusion of the alkaline complex (ca. 1.49?Ga). Primary compositional sector and oscillatory zoning in these eudialyte crystals shows core-to-rim enrichment in rare-earth elements and significant fractionation of K/Rb, Y/Ho, Zr/Hf, and Nb/Ta, which we attribute to crystallisation under influence of complexing ligands in a confined volume. We argue that these mineralised pegmatoid veins formed by low-temperature (<550?°C) partial melting of the agpaitic host rock during an early Sveconorwegian (Grenvillian) metamorphic overprinting event. Given the challenge of directly dating rare-earth ore minerals by conventional methods, modification of rare-earth mineral deposits may be more widespread than already assumed, which shows the importance of investigations that date the rare-earth minerals themselves.
Journal of Geophysical Research: Solid Earth, doi: 10.1029/2018JB016012
Africa, South Africa
diamond inclusions
Abstract: Here we report the first results from elastic geobarometry applied to a kyanite inclusion entrapped within an eclogitic diamond (from Voorspoed mine, South Africa) using micro-Raman and Fourier transform infrared spectroscopy, electron microprobe analysis, ab initio calculations, and finite element modeling. Application of elastic geobarometry to very elastically anisotropic kyanite inclusions is challenging, as current models do not allow for elastic anisotropy. In order to minimize the effects of anisotropy, we have explored the effects of deviatoric stress on Raman modes via ab initio density functional theory. The results allowed us to select the Raman mode (at ca. 638 cm-1) that is the least sensitive to deviatoric stress. The shift of this band in the inclusion while still trapped within the diamond relative to the inclusion in air (once liberated) was used under hydrostatic approximation to determine a residual pressure on the inclusion of 0.184 ± 0.045 GPa and an entrapment pressure of 5.2 ± 0.3 GPa (~160 km depth) for an FTIR N-aggregation residence temperature of 1119 ± 50 °C. This is the first geothermobarometric determination for a diamond from the Voorspoed kimberlite. It overlaps with P-T estimates obtained by traditional chemical geobarometry for diamonds from other kimberlites from the Kaapvaal craton, suggesting that the hydrostatic approximation does not introduce significant errors in the geobarometric evaluation. Our protocol of Raman peak selection can be used for geobarometry of further kyanite-bearing diamonds and may provide a guide for more robust geobarometry of other types of mineral inclusions in diamonds, both eclogitic and peridotitic.
Abstract: Diamonds and their inclusions are unique fragments of deep Earth, which provide rare samples from inaccessible portions of our planet. Inclusion-free diamonds cannot provide information on depth of formation, which could be crucial to understand how the carbon cycle operated in the past. Inclusions in diamonds, which remain uncorrupted over geological times, may instead provide direct records of deep Earth’s evolution. Here, we applied elastic geothermobarometry to a diamond-magnesiochromite (mchr) host-inclusion pair from the Udachnaya kimberlite (Siberia, Russia), one of the most important sources of natural diamonds. By combining X-ray diffraction and Fourier-transform infrared spectroscopy data with a new elastic model, we obtained entrapment conditions, Ptrap?=?6.5(2) GPa and Ttrap?=?1125(32)-1140(33) °C, for the mchr inclusion. These conditions fall on a ca. 35?mW/m2 geotherm and are colder than the great majority of mantle xenoliths from similar depth in the same kimberlite. Our results indicate that cold cratonic conditions persisted for billions of years to at least 200?km in the local lithosphere. The composition of the mchr also indicates that at this depth the lithosphere was, at least locally, ultra-depleted at the time of diamond formation, as opposed to the melt-metasomatized, enriched composition of most xenoliths.
The diamond bearing territories of Africa and their importance for expansion of the raw material base of the Russian diamond mining industry. ***IN RUS
Mineral Resources of Russia: economics and Management *** IN RUS, No. 6, pp. 66-72. pdf
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0628-1 14p.
Africa, Angola
kimberlites
Abstract: Based on a comprehensive analysis of kimberlite pipes of Angola, including the near surface structural setting, deep lithospheric structure, pipe morphology and emplacement, mineralogical and petrographic features, diamond characteristics and locations of secondary deposits four geographical regions have been outlined within Angola representing four types of diamond bearing potential. These areas include high diamond bearing potential pipes, possible potential, no potential, and unclear potential areas. It was found that the depth of magmatism and diamond potential of kimberlites increases from the Atlantic coast in southwestern Angola into the continent in the north-easterly direction. Areas prospective for the discovery of new primary diamond deposits have been identified.
Chemical Geology, DOI:101016/ j.chemgeo.2020.119464
Mantle
peridotite
Abstract: The lithospheric mantle should be depleted in base- and precious-metals as these elements are transferred to the crust during partial melting. However, some melt-depleted mantle peridotites are enriched in these ore-forming elements. This may reflect re-fertilization of the mantle lithosphere and/or sequestering of these elements by residual mantle phase(s). Both processes remain poorly understood because of the low abundances of incompatible elements in peridotite and the nugget-like distribution of digestion-resistant mantle phases that pose analytical challenges for conventional geochemical methods. Herein we report new major and trace element concentrations for a suite of mantle peridotite and pyroxenite samples from the Late Permian to Middle Triassic Nahlin ophiolite (Cache Creek terrane, British Columbia, Canada) using Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICPMS) analysis of nanoparticulate powders and olivine. Compatible to moderately incompatible element concentrations suggest that Nahlin ophiolite peridotites represent residues after =20% melt extraction. Pyroxenite dykes and replacive dunite bands are folded and closely intercalated with residual harzburgite. These field relationships, coupled with the presence of intergranular base metal sulphide, clinopyroxene and Cr-spinel at the microscale, point to percolating melts that variably re-fertilized melt-depleted mantle peridotite. Radiogenic Pb (206Pb/204Pb?=?15.402-19.050; 207Pb/204Pb?=?15.127-15.633; 208Pb/204Pb?=?34.980-38.434; n?=?45) and Os (187Os/188Os 0.1143-0.5745; n?=?58) isotope compositions for a subset of melt-depleted peridotite samples further support metasomatic re-fertilization of these elements. Other ore-forming elements are also implicated in these metasomatic reactions because some melt-depleted peridotite samples are enriched relative to the primitive mantle, opposite to their expected behaviour during partial melting. New LA-ICPMS analysis of fresh olivine further demonstrates that a significant proportion of the highly incompatible element budget for the most melt-depleted rocks is either hosted by, and/or occurs as trapped inclusions within, the olivine-rich residues. Trapped phases from past melting and/or re-fertilization events are the preferred explanation for unradiogenic Pb isotope compositions and Paleozoic to Paleoproterozoic Re-depletion model ages, which predate the Nahlin ophiolite by over one billion years.
Abstract: How the Earth's continental crust was formed in the Hadean eon is a subject of considerable debates [1-4]. For example, shallow hydrous peridotites [2,5], in particular the Hadean Earth's serpentinites [6], are potentially important ingredients in the creation of the continental ptoto-crust, but the mechanisms of this formation remain elusive. In this work, experiments to explore serpentinite-basalt interaction under conditions of the Hadean Earth were conducted. Kinetic runs lasting 0.5 to 48 hours at 0.2 to 1.0 GPa and 1250 to 1300°C reveal dehydration of serpentinite and release of a Si-Al-Na-K-rich aqueous fluid. For the first time, generation of heterogeneous hydrous silicic melts (56 to 67 wt% SiO2) in response to the fluid-assisted fertilisation and the subsequent partial melting of the dehydrated serpentinite has been discovered. The melts produced at 0.2 GPa have compositions similar to those of the bulk continental crust [2,3]. These new findings imply that the Earth's sialic proto-crust may be generated via fluid-assisted melting of serpentinized peridotite at shallow depths (=7 km) that do not require plate subduction during the Hadean eon. Shallow serpentinite dehydration and melting may be the principal physico-chemical processes affecting the earliest lithosphere.
Making Earth's continental crust from serpentinite and basalt.
American Mineralogist, Vol. 105, pp. 1662-1671. pdf
Mantle
melting
Abstract: Zircon is the most frequently used mineral for dating terrestrial and extraterrestrial rocks. However, the system of zircon in mafic/ultramafic melts has been rarely explored experimentally and most existing models based on the felsic, intermediate and/or synthetic systems are probably not applicable for prediction of zircon survival in terrestrial shallow asthenosphere. In order to determine the zircon stability in such natural systems, we have performed high-temperature experiments of zircon dissolution in natural mid-ocean ridge basaltic and synthetic haplobasaltic melts coupled with in situ electron probe microanalyses of the experimental products at high current.
Taking into account the secondary fluorescence effect in zircon glass pairs during electron microprobe analysis, we have calculated zirconium diffusion coefficient necessary to predict zircon survival in asthenospheric melts of tholeiitic basalt composition. The data imply that typical 100 micron zircons dissolve rapidly (in 10 hours) and congruently upon the reaction with basaltic melt at mantle pressures. We observed incongruent (to crystal ZrO2 and SiO2 in melt) dissolution of zircon in natural mid-ocean ridge basaltic melt at low pressures and in haplobasaltic melt at elevated pressure. Our experimental data raise questions about the origin of zircons in mafic and ultramafic rocks, in particular, in shallow oceanic asthenosphere and deep lithosphere, as well as the meaning of the zircon-based ages estimated from the composition of these minerals. Large size zircon megacrysts in kimberlites, peridotites, alkali basalts and other magmas suggest the fast transport and short interaction between zircon and melt.The origin of zircon megacrysts is likely related to metasomatic addition of Zr into mantle as any mantle melting episode should obliterate them.
Temporal distribution of the ultramafic-alkalic and alkalic rocks withIn the Russian, Siberian and North American ancient platforms and theirsurroundings
Geological Survey of Wyoming Open File Report, No. 89-9, 33p
Abstract: Global deep-time plate motion models have traditionally followed a classical rigid plate approach, even though plate deformation is known to be significant. Here we present a global Mesozoic-Cenozoic deforming plate motion model that captures the progressive extension of all continental margins since the initiation of rifting within Pangea at ~240 Ma. The model also includes major failed continental rifts and compressional deformation along collision zones. The outlines and timing of regional deformation episodes are reconstructed from a wealth of published regional tectonic models and associated geological and geophysical data. We reconstruct absolute plate motions in a mantle reference frame with a joint global inversion using hotspot tracks for the last 80 million years and minimizing global trench migration velocities and net lithospheric rotation. In our optimized model net rotation is consistently below 0.2°/Myr, and trench migration scatter is substantially reduced. Distributed plate deformation reaches a Mesozoic peak of 30 million km2 in the Late Jurassic (~160-155 Ma), driven by a vast network of rift systems. After a mid-Cretaceous drop in deformation it reaches a high of 48 million km2 in the Late Eocene (~35 Ma), driven by the progressive growth of plate collisions and the formation of new rift systems. About a third of the continental crustal area has been deformed since 240 Ma, partitioned roughly into 65% extension and 35% compression. This community plate model provides a framework for building detailed regional deforming plate networks and form a constraint for models of basin evolution and the plate-mantle system.
Muller, D., Zahirovic, S., Williams, S.E., Cannon, J., Seton, M., Bower, D.J., Tetley, M., Heine, C., Le Breton, E., Liu, S., Russell, S.H.J., Yang, T., Leonard, J., Gurnis, M.
Abstract: Global deep-time plate motion models have traditionally followed a classical rigid plate approach, even though plate deformation is known to be significant. Here we present a global Mesozoic-Cenozoic deforming plate motion model that captures the progressive extension of all continental margins since the initiation of rifting within Pangea at ~240 Ma. The model also includes major failed continental rifts and compressional deformation along collision zones. The outlines and timing of regional deformation episodes are reconstructed from a wealth of published regional tectonic models and associated geological and geophysical data. We reconstruct absolute plate motions in a mantle reference frame with a joint global inversion using hot spot tracks for the last 80 million years and minimizing global trench migration velocities and net lithospheric rotation. In our optimized model, net rotation is consistently below 0.2°/Myr, and trench migration scatter is substantially reduced. Distributed plate deformation reaches a Mesozoic peak of 30 × 106 km2 in the Late Jurassic (~160-155 Ma), driven by a vast network of rift systems. After a mid-Cretaceous drop in deformation, it reaches a high of 48 x 106 km2 in the Late Eocene (~35 Ma), driven by the progressive growth of plate collisions and the formation of new rift systems. About a third of the continental crustal area has been deformed since 240 Ma, partitioned roughly into 65% extension and 35% compression. This community plate model provides a framework for building detailed regional deforming plate networks and form a constraint for models of basin evolution and the plate-mantle system.
Geochimica et Cosmochimica Acta, Vol. 232, pp. 82-100.
Mantle
geochemistry
Abstract: We have analyzed ancient atmospheric gases trapped in fluid inclusions contained in minerals of Archean (3.3?Ga) to Paleozoic (404?Ma) rocks in an attempt to document the evolution of the elemental composition and isotopic signature of the atmosphere with time. Doing so, we aimed at understanding how physical and chemical processes acted over geological time to shape the modern atmosphere. Modern atmospheric xenon is enriched in heavy isotopes by 30-40‰ u-1 relative to Solar or Chondritic xenon. Previous studies demonstrated that, 3.3?Ga ago, atmospheric xenon was isotopically fractionated (enriched in the light isotopes) relative to the modern atmosphere, by 12.9?±?1.2 (1s) ‰ u-1, whereas krypton was isotopically identical to modern atmospheric Kr. Details about the specific and progressive isotopic fractionation of Xe during the Archean, originally proposed by Pujol et al. (2011), are now well established by this work. Xe isotope fractionation has evolved from 21‰ u-1 at 3.5?Ga to 12.9‰ u-1 at 3.3?Ga. The current dataset provides some evidence for stabilization of the Xe fractionation between 3.3 and 2.7?Ga. However, further studies will be needed to confirm this observation. After 2.7?Ga, the composition kept evolving and reach the modern-like atmospheric Xe composition at around 2.1?Ga ago. Xenon may be the second atmospheric element, after sulfur, to show a secular isotope evolution during the Archean that ended shortly after the Archean-Proterozoic transition. Fractionation of xenon indicates that xenon escaped from Earth, probably as an ion, and that Xe escape stopped when the atmosphere became oxygen-rich. We speculate that the Xe escape was enabled by a vigorous hydrogen escape on the early anoxic Earth. Organic hazes, scavenging isotopically heavy Xe, could also have played a role in the evolution of atmospheric Xe. For 3.3?Ga-old samples, Ar-N2 correlations are consistent with a partial pressure of nitrogen (pN2) in the Archean atmosphere similar to, or lower than, the modern one, thus requiring other processes than a high pN2 to keep the Earth's surface warm despite a fainter Sun. The nitrogen isotope composition of the atmosphere at 3.3?Ga was already modern-like, attesting to inefficient nitrogen escape to space since that time.
Geochimica et Cosmochimica Acta, Vol. 244, pp. 56-85.
Mantle
convection
Abstract: Atmospheric xenon is strongly mass fractionated, the result of a process that apparently continued through the Archean and perhaps beyond. Previous models that explain Xe fractionation by hydrodynamic hydrogen escape cannot gracefully explain how Xe escaped when Ar and Kr did not, nor allow Xe to escape in the Archean. Here we show that Xe is the only noble gas that can escape as an ion in a photo-ionized hydrogen wind, possible in the absence of a geomagnetic field or along polar magnetic field lines that open into interplanetary space. To quantify the hypothesis we construct new 1-D models of hydrodynamic diffusion-limited hydrogen escape from highly-irradiated CO2-H2-H atmospheres. The models reveal three minimum requirements for Xe escape: solar EUV irradiation needs to exceed that of the modern Sun; the total hydrogen mixing ratio in the atmosphere needs to exceed 1% (equiv. to CH4); and transport amongst the ions in the lower ionosphere needs to lift the Xe ions to the base of the outflowing hydrogen corona. The long duration of Xe escape implies that, if a constant process, Earth lost the hydrogen from at least one ocean of water, roughly evenly split between the Hadean and the Archean. However, to account for both Xe’s fractionation and also its depletion with respect to Kr and primordial 244Pu, Xe escape must have been limited to small apertures or short episodes, which suggests that Xe escape was restricted to polar windows by a geomagnetic field, or dominated by outbursts of high solar activity, or limited to transient episodes of abundant hydrogen, or a combination of these. Xenon escape stopped when the hydrogen (or methane) mixing ratio became too small, or EUV radiation from the aging Sun became too weak, or charge exchange between Xe+ and O2 rendered Xe neutral. In our model, Xe fractionation attests to an extended history of hydrogen escape and Earth oxidation preceding and ending with the Great Oxidation Event (GOE).
Abstract: Formation of hydrocarbons by reactions of hydrogenbearing fluids with carbon [1] (13C soot, graphite, or diamond), carbonate-bearing pelites [2] and iron carbides (Fe3C and Fe7C3) [3] was simulated at 5.5-7.8 GPa and 1100- 1400°C, fH2 in Pt and Au capsules being controlled at the Mo+MoO2+H2O or Fe+FeO+H2O equilibria. For the first time, formation of hydrocarbons from inorganic compounds was proved by the reaction of 13C with hydrogen, which yielded isotopically pure alkanes. The greatest amounts of HCs (CH4/C2H6 < 1, CH4/C3H8 and CH4/C4H10 = 10) formed at 1400°C in the 10-hr run. The amount of HCs synthesized at 1200°C was twice smaller. The rate of HCs formation was slowest in runs with diamond. At 1200 °C, light alkanes (C1˜C2>C3>C4) formed either by direct hydrogenation of Fe3C or Fe7C3, or by hydrogenation of graphite/diamond in the presence of Fe3C, Fe7C3. The CH4/C2H6 ratio in the fluids decreased from 5 to 0.5 with decreasing iron activity and the C fraction increased in the series: Fe-Fe3C?Fe3C- Fe7C3?Fe7C3-graphite?graphite-Fe3C-magnesite and Fe3C-H2O-CO2 systems at 1200 °C yielded magnesiowüstite and wüstite, respectively, and both produced C-rich Fe7C3 and mainly light alkanes (C1˜C2>C3>C4). In the experiments containing pelites methaneimine (CH3N) was found to be the main N-bearing compound. The experiments have provided the first unambiguous evidence that volatile-rich and reduced mantles of terrestrial planets (at fO2 near or below IW) provided favorable conditions for abiotic generation of complex hydrocarbon systems that predominantly contain light alkanes. The conditions favorable for HC formation exist in earth mantle, where slab-derived H2O-, CO2- and carbonate-bearing fluids interact with metal-saturated mantle.
Deijanin, B., Simic, D., Zaitsev, A., Chapman, J., Dobrinets, I., Widemann, A., Del Re, N., Middleton, T., Dijanin, E., Se Stefano, A.
Characterization of pink diamonds of different origin: natural ( Argyle, non-Argyle), irradiated and annealed, treated with multi-process, coated and synthetic.
Diamond and Related Materials, Vol. 17, 7-10, pp. 1169-1178.
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.
The age and localization of kimberlite magmatism in the Yakutian kimberlite Province: constraints from isotope geochronology - an overview.
Proceedings of the 10th. International Kimberlite Conference, Vol. 1, Special Issue of the Journal of the Geological Society of India,, Vol. 1, pp. 225-234.
Abstract: Black diamonds with poor transparency due to an intensity of mineral inclusions and fractures are routinely traded in the gem market today. Although the inclusions and fractures are of natural origin this type of diamond is often heated to create a more uniform black color by further graphitizing these inclusions and fractures. Graphitization is often prominent at these fractures resulting in poor quality heavily fractured material. After nitrogen hydrogen is the most common impurity in natural diamond and is often responsible for a gem quality diamonds color. Color in diamond related or attributed to the hydrogen impurity can range from brown to green and gray. These colors are often undesirable to the gem trade and consumers. Recently GIA laboratories have seen a lot of faceted “Black” diamonds (graded as Fancy Black on GIA’s color scale) for identification. These diamonds are hydrogen rich and it is suspected that this material is treated (heated). Probably unattractive grayish green brown material that is virtually worthless in the gem trade before treatment. With such large quantities of this treated material available a serious threat and identification problem is posed to the Gem Diamond industry. Three faceted round cut hydrogen rich diamonds (0.30, 0.52 and 0.58 carats) colored by dense hydrogen clouds giving them a murky grayish appearance have been documented and systematically heated. A black color identical to that of the suspected treated black diamonds has been achieved, thus confirming this coloration treatment and new identification techniques to detect it. These treated black diamonds have a uniform color and lack the heavy fracturing and surface graphitization of typical treated black diamonds. Heating conditions and techniques will be discussed and we report on this new type of material and gem stone treatment.
Diamond and Related Materials, Vol. 71, pp. 20-29,
Africa, Zimbabwe
Deposit - Marange
Abstract: This study gives an analysis of the effect of low-pressure, high-temperature annealing on the infrared, Raman, and photoluminescence (PL) features, as well as the inclusion characteristics, of cubo-octahedral diamond plates from the Marange deposits in Zimbabwe. The samples showed strong inclusion-related zoning which consists of micron-sized particles identified as graphite and these grew noticeably larger with annealing at temperatures of 300 °C to 1700 °C. Within the natural diamonds, the graphite inclusions (detected by Raman spectroscopy) had a grain size of approximately 1 µm, which increased to 3 µm after 1200 °C and 14 µm after 1700 °C annealing and their hexagonal morphology was discernible. From the geometry of these grains, we determined that they were oriented within the {111} family of planes. The infrared absorption and PL spatial maps were collected after every temperature step to study the effects of annealing on the defects, and photomicrographs and Raman spectra were collected to study the graphite inclusions. The graphitic inclusions grew much larger as the stressed diamond surrounding them converted to graphite. Many nitrogen-related optical centers, including NV- and H3 are no longer detected after high temperature annealing within the cuboid regions as these may have been transformed to hydrogen-bearing complexes such as NVH and N2VH. The presence of CH4 is detected in the unannealed Marange diamonds, but was no longer observed in Raman spectra after 1200 °C annealing. This CH4 disappearance along with changes in inclusion morphology could provide a method to detect heat treatment if these mixed-habit samples are sourced to create treated black gem diamond.
Diamond and Related Materials, Vol. 77, pp. 159-170.
Technology
diamond morphology
Abstract: Low-pressure, high-temperature (LPHT) annealing of yellow-to-brown type Ia natural diamonds was performed to monitor its effects on optical centers within diamond, changes in the observed color, and to assess the process's viability as a commercial gem treatment. With LPHT annealing only, the mostly brown diamonds showed a shift towards yellow coloration; Vis-NIR absorption spectra showed this change was due to a modest increase in H3 intensity. Even at long annealing times (24 h at 1800 °C) or annealing at high temperatures (2000 °C for five minutes), the diamonds did not significantly lose brown coloration. LPHT annealing showed itself as an ineffective means to break apart the vacancy clusters causing the brown color or causing nitrogen disaggregation, which resulted in only a small H3 generation. With LPHT annealing, “amber centers”—a group of several independent bands in the IR between 4200 and 4000 cm- 1 that disappear with HPHT annealing—were seen to anneal out gradually at various temperatures from 1700 to 2000 °C. In contrast, high-pressure, high-temperature (HPHT) annealing effectively removes brown color at similar time/temperature conditions. Without the high stabilizing pressure provided by HPHT annealing techniques, the LPHT annealing showed pronounced damage on inclusions and dramatic surface etching. In subsequent experiments, LPHT annealing was used as a follow-up to laboratory irradiation. The irradiation-related vacancies created greater concentrations of H3 and the vacancy-assisted disaggregation of nitrogen created donors which led to a high concentration of H2 centers. This combination of defects resulted in a pronounced and favorable shift towards saleable yellow colors due to an increase in H3 and a dramatic increase in the H2 center, which led to the suppression of the remaining brownish component. The annealing characteristics for many centers detected by Vis-NIR absorption spectroscopy, FTIR absorption spectroscopy, and photoluminescence spectroscopy were chronicled throughout the study and compared with other LPHT annealing studies and HPHT annealing experiments.
Diamond and Related Materials, doi:101016/j.diamond.2018.07.017
Russia
synthetics
Abstract: Nitrogen-doped CVD diamond treated with electron irradiation and subsequent annealing at temperatures from 860 to 1900?°C was studied using fluorescence imaging, optical absorption and photoluminescence. It was found that nitrogen impurity produces many optical centers active throughout the infrared and visible spectral ranges. The most prominent of them active in IR spectral range are the centers related to nitrogen-hydrogen complexes. They produce absorption lines at 2827, 2874, 2906, 2949, 2990, 3031, 3107, 3123 and 3310?cm-1. Two characteristic absorptions at wavenumbers 1293?cm-1 and 1341?cm-1 were tentatively ascribed to a modified form of nitrogen A-aggregates. In the visible and near IR spectral ranges, characteristic nitrogen-related centers have zero-phonon lines (ZPLs) at 457, 462, 489, 498, 722.5, 852.5, 865.5, 868.5, 908, 921.5 and 924.5?nm. Some of them, e.g. 457, 462 and 498?nm centers, are unique of CVD diamond. It has been confirmed that the brightest pink color of electron-irradiated nitrogen-doped CVD diamond is produced by annealing at temperatures about 1000?°C. Annealing at temperatures over 1600?°C destroys the irradiation-induced pink color. It was found that the center 489?nm is a major absorption feature in the visible spectral range of electron-irradiated, nitrogen-doped CVD diamond. Green color of electron-irradiated, nitrogen-doped CVD diamond is caused by combined absorption of GR1 center and 489?nm center. It has been confirmed that NV defects produced in CVD diamond during growth are very temperature stable. They survive heating at temperatures at least 2000?°C. In contrast, NV defects produced by irradiation may anneal out at temperatures as low as 1600?°C. This much lower thermal stability of the radiation-induced NV defects is the result of their interaction with other radiation defects produced in their vicinity. A conclusion has been made that in nitrogen-doped CVD diamonds nitrogen atoms may form clusters. These clusters are probably the origin of the broad band luminescence at wavelengths 360, 390, 535 and 720?nm and a strong broadening of ZPLs of many optical centers.
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.
Gems & Gemology, Sixth International Gemological Symposium Vol. 54, 3, 1p. Abstract p. 304-5.
Global
synthetics
Abstract: In diamond grown by the CVD method, nitrogen behaves differently than it does in natural and HPHT-grown diamond. The most striking peculiarities are low efficiency of doping, formation of unique optical centers over a wide spectral range from the ultraviolet (UV) to the IR regions, and formation of unusual defects related to aggregated nitrogen. In order to gain a better insight into this problem, several nitrogen-doped specimens grown in GIA’s CVD diamond lab and a few commercial yellow CVD-grown diamonds have been studied in their as-grown (asreceived) state and after electron irradiation and annealing at temperatures up to 1900°C (low-pressure, high-temperature treatment). We found that the brightest pink color of electron-irradiated nitrogen-doped CVD-grown diamond is produced by the NV– center after annealing at temperatures of about 1000°C. Annealing at temperatures over 1600°C destroys the irradiation-induced pink color (figure 1). The most prominent optical centers in the IR spectral region (figure 2, left) produced absorptions at 2828, 2874, 2906, 2949, 3031, 3107, 3123, and 3310 cm–1 (latter two not shown). These are ascribed to nitrogen-hydrogen complexes. Two characteristic absorption features at 1293 and 1341 cm–1 (figure 2, right) are unique to CVD diamond. They are tentatively ascribed to a modified form of nitrogen A-aggregates. In the visible and NIR spectral ranges, characteristic nitrogenrelated centers have zero-phonon lines (ZPLs) at 457, 462, 489, 498, 647, 722.5, 852.5, 865.5, 868.5, 908, 921.5, and 924.5 nm. The 489 nm feature is a major color center of electron-irradiated, nitrogen-doped CVD-grown diamond. This center, together with the GR1 center, is responsible for the green color in this material. An assumption is made that N atoms may form clusters in highly nitrogen-doped CVD-grown diamonds. These clusters may result in broad-band luminescence at wavelengths of 360, 390, 535, and 720 nm and a strong broadening of the ZPLs of many optical centers
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.
Mineralogy of heavy minerals concentrates from the unconsolidated deposits of Eledoi and Pello Hill volcanic cones ( Gelai volcano): first preliminary data
Peralk-Carb 2011, workshop held Tubingen Germany June 16-18, Poster
Mineralogy of heavy minerals concentrates from the unconsolidated deposits of Eeldoi and Pello Hill volcanic cones (Gelai volcano, northern Tanzania) prel.
Peralk-Carb 2011... workshop June 16-18, Tubingen, Germany, Abstract p.111-112.
Mineralogy of heavy minerals concentrates from the unconsolidated deposits of Eeldoi and Pello Hill volcanic cones (Gelai volcano, northern Tanzania) prel.
Peralk-Carb 2011... workshop June 16-18, Tubingen, Germany, Abstract p.111-112.
Flourine , yttrium and lanthaide rich cerianite (Ce) from carbonatitic rocks of the Kerimasi volcano and surrounding explosive craters Gregory Rift Tanzania.
Mineralogical Magazine, Vol. 75, 6, pp. 2813-2822.
Mangler, M.F., Marks, M.A.W., Zaitsev, A.N., Eby, G.N., Markl, G.
Halogens (F, Cl and Br) at Oldoinyo Lengai volcano ( Tanzania): effects of magmatic differentiation, silicate, natrocarbonatite melt seperation and surface alteration of natrocarbonatite.
Rare earth elements in phoscorites and carbonatites of the Devonian Kola alkaline province, Russia: examples from Kovdor, Khibina, Vuoriyarvi and Turiy Mys complexes.
Rare earth elements in phoscorites and carbonatites of the Devonian Kola alkaline province, Russia: examples from Kovdor, Khibina, Vuoriyarvi and Turiy Mys complexes.
Rare earth elements in phoscorites and carbonatites of the Devonian Kola alkaline province, Russia: examples from Kovdor, Khibina, Vuoriyarvi and Turiy Mys complexes.
Abstract: Galena from four REE-rich (Khibina, Sallanlatvi, Seblyavr, Vuoriyarvi) and REE-poor (Kovdor) carbonatites, as well as hydrothermal veins (Khibina) all from the Devonian Kola Alkaline Province of northwestern Russia was analysed for trace elements and Pb and S isotope compositions. Microprobe analyses show that the only detectable elements in galena are Bi and Ag and these vary from not detectable to 2.23 and not detectable to 0.43 wt.% respectively. Three distinct galena groups can be recognized using Bi and Ag contents, which differ from groupings based on Pb isotope data. The Pb isotope ratios show significant spread with 206Pb/204Pb ratios (16.79 to 18.99), 207Pb/204Pb (15.22 to 15.58) and 208Pb/204Pb ratios (36.75 to 38.62). A near-linear array in a 207Pb/204Pb vs. 206Pb/204Pb ratio diagram is consistent with mixing between distinct mantle sources, one of which formed during a major differentiation event in the late Archaean or earlier. The S isotopic composition (d34S) of galena from carbonatites is significantly lighter (–-6.7 to -–10.3% Canyon Diablo Troilite (CDT) from REE-rich Khibina, Seblyavr and Vuoriyarvi carbonatites, and - 3.2% CDT from REE-poor Kovdor carbonatites) than the mantle value of 0%. Although there is no correlation between S and any of the Pb isotope ratios, Bi and Ag abundances correlate negatively with d34S values. The variations in the isotopic composition of Pb are attributed to partial melting of an isotopically heterogeneous mantle source, while those of d34S (together with Bi and Ag abundances) are considered to be process driven. Although variation in Pb isotope values between complexes might reflect different degrees of interaction between carbonatitic melts and continental crust or metasomatized lithosphere, the published noble gas and C, O, Sr, Nd and Hf isotopic data suggest that the variable Pb isotope ratios are best attributed to isotopic differences preserved within a sub-lithospheric mantle source. Different Pb isotopic compositions of galena from the same complex are consistent with a model of magma replenishment by carbonatitic melts/fluids each marked by quite different Pb isotopic compositions.
Abstract: Carbonatites are nominally igneous rocks, whose evolution commonly involves also a variety of postmagmatic processes, including exsolution, subsolidus re-equilibration of igneous mineral assemblages with fluids of different provenance, hydrothermal crystallization, recrystallization and tectonic mobilization. Petrogenetic interpretation of carbonatites and assessment of their mineral potential are impossible without understanding the textural and compositional effects of both magmatic and postmagmatic processes on the principal constituents of these rocks. In the present work, we describe the major (micro)textural characteristics of carbonatitic calcite and dolomite in the context of magma evolution, fluid-rock interaction, or deformation, and provide information on the compositional variation of these minerals and its relation to specific evolutionary processes.
Russian Geology and Geophysics, Vol. 56, pp. 1717-1737.
Africa, Tanzania
Deposit - Oldoinyo Lengai
Abstract: The paper is concerned with study of melt inclusions in minerals of ijolite xenoliths at Oldoinyo Lengai Volcano. Melt inclusions with different phase compositions occur in forsterite macrocrysts and in diopside, nepheline, fluorapatite, Ti-andradite, and Ti-magnetite crystals. Nepheline contains primary melt inclusions (silicate glass + gas-carbonate globule ± submicron globules ± sulfide globule ± daughter/trapped phases, represented by diopside, fluorapatite, Ti-andradite, and alumoakermanite). The gas-carbonate globule consists of a gas bubble surrounded by a fine-grained aggregate of Na-Ca-carbonates (nyerereite and gregoryite). Fluorapatite contains primary carbonate-rich melt inclusions in the core, which consist of nyerereite, gregoryite, thenardite, witherite, fluorite, villiaumite, and other phases. Their mineral composition is similar to natrocarbonatites. Primary melt inclusions (glass + gas bubble ± daughter phases) are rare in diopside and Ti-andradite. Diopside and forsterite have trails of secondary carbonate-rich inclusions. Besides the above minerals, these inclusions contain halite, sylvite, neighborite, Na-Ca-phosphate, alkali sulfates, and other rare phases. In addition, diopside contains sulfide inclusions (pyrrhotite ± chalcopy- rite ± djerfisherite ± galena ± pentlandite). The chemical compositions of silicate glasses in the melt inclusions vary widely. The glasses are characterized by high Na, K, and Fe contents and low Al contents. They have high total alkali contents (16-23 wt.% Na2O + K2O) and peralkalinity index [(Na + K)/Al] ranging from 1.1 to 7.6. The carbonate-rich inclusions in the ijolite minerals are enriched in Na, P, S, and Cl. The data obtained indicate that the parental melt in the intermediate chamber was heterogeneous and contained silicate, natrocarbonate, and sulfide components during the ijolite crystallization. According to heating experiments with melt inclusions, silicate-carbonate liquid immiscibility occurred at temperature over 580 °C.
Abstract: The Late Cretaceous (ca. 100 Ma) diamondiferous Fort à la Corne (FALC) kimberlite field in the Saskatchewan (Sask) craton, Canada, is one of the largest known kimberlite fields on Earth comprising essentially pyroclastic kimberlites. Despite its discovery more than two decades ago, petrological, geochemical and petrogenetic aspects of the kimberlites in this field are largely unknown. We present here the first detailed petrological and geochemical data combined with reconnaissance Nd isotope data on drill-hole samples of five major kimberlite bodies. Petrography of the studied samples reveals that they are loosely packed, clast-supported and variably sorted, and characterised by the presence of juvenile lapilli, crystals of olivine, xenocrystal garnet (peridotitic as well as eclogitic paragenesis) and Mg-ilmenite. Interclast material is made of serpentine, phlogopite, spinel, carbonate, perovskite and rutile. The mineral compositions, whole-rock geochemistry and Nd isotopic composition (Nd: + 0.62 to - 0.37) are indistinguishable from those known from archetypal hypabyssal kimberlites. Appreciably lower bulk-rock CaO (mostly < 5 wt%) and higher La/Sm ratios (12-15; resembling those of orangeites) are a characteristic feature of these rocks. Their geochemical composition excludes any effects of significant crustal and mantle contamination/assimilation. The fractionation trends displayed suggest a primary kimberlite melt composition indistinguishable from global estimates of primary kimberlite melt, and highlight the dominance of a kimberlite magma component in the pyroclastic variants. The lack of Nb-Ta-Ti anomalies precludes any significant role of subduction-related melts/fluids in the metasomatism of the FALC kimberlite mantle source region. Their incompatible trace elements (e.g., Nb/U) have OIB-type affinities whereas the Nd isotope composition indicates a near-chondritic to slightly depleted Nd isotope composition. The Neoproterozoic (~ 0.6-0.7 Ga) depleted mantle (TDM) Nd model ages coincide with the emplacement age (ca. 673 Ma) of the Amon kimberlite sills (Baffin Island, Rae craton, Canada) and have been related to upwelling protokimberlite melts during the break-up of the Rodinia supercontinent and its separation from Laurentia (North American cratonic shield). REE inversion modelling for the FALC kimberlites as well as for the Jericho (ca. 173 Ma) and Snap Lake (ca. 537 Ma) kimberlites from the neighbouring Slave craton, Canada, indicate all of their source regions to have been extensively depleted (~ 24%) before being subjected to metasomatic enrichment (1.3-2.2%) and subsequent small-degree partial melting. These findings are similar to those previously obtained on Mesozoic kimberlites (Kaapvaal craton, southern Africa) and Mesoproterozoic kimberlites (Dharwar craton, southern India). The striking similarity in the genesis of kimberlites emplaced over broad geological time and across different supercontinents of Laurentia, Gondwanaland and Rodinia, highlights the dominant petrogenetic role of the sub-continental lithosphere. The emplacement of the FALC kimberlites can be explained both by the extensive subduction system in western North America that was established at ca. 150 Ma as well as by far-field effects of the opening of the North Atlantic ocean during the Late Cretaceous.
Mineralogy and Petrology, Vol. 111, 3, pp. 373-381.
Africa, Tanzania
mineralogy
Abstract: Jörgkellerite, ideally Na3Mn3+ 3(PO4)2(CO3)O2•5H2O, is a new layered phosphate-carbonate from the Oldoinyo Lengai volcano in the Gregory Rift (northern Tanzania). The mineral occurs as spherulites, up to 200 µm in diameter, consisting of plates up to 10 µm in thickness in shortite-calcite and calcite carbonatites. Jörgkellerite is brown with a vitreous lustre and has a perfect micaceous cleavage on {001}, Mohs hardness is 3. The calculated density is 2.56 g/cm3. Jörgkellerite is uniaxial (-), ? = 1.700(2), ? = 1.625(2) (Na light, 589 nm) with distinct pleochroism: O = dark brown, E = light brown. The empirical formula of the mineral (average of 10 electron microprobe analyses) is (Na2.46K0.28Ca0.08Sr0.04Ba0.02)S2.88(Mn3+ 2.39Fe3+ 0.56)S2.95((PO4)1.95(SiO4)0.05))S2.00(CO3)(O1.84(OH)0.16)S2.00•5H2O. The oxidation state of Mn has been determined by XANES. Jörgkellerite is trigonal, space group P-3, a = 11.201(2) Å, c = 10.969(2) Å, V = 1191.9(7) Å3 and Z = 3. The five strongest powder-diffraction lines [d in Å, (I/I o), (hkl)] are: 10.970 (100) (001), 5.597 (15) (002), 4.993 (8) (111), 2.796 (14) (220) and 2.724 (20) (004). The crystal structure is built up of the layers composed of disordered edge-sharing [MnO6] octahedra. Each fourth Mn site in octahedral layer is vacant that results in appearance of ordered system of hexagonal "holes" occupied by (CO3) groups. The overall composition of the layer can be expressed as [Mn3O8(CO3)]. These manganese-carbonate layers are linked in the third dimension by (PO4) tetrahedra and Na-polyhedra. The origin of jörgkellerite is related to low-temperature oxidative alteration of gregoryite-nyerereite carbonatites.
Neues Jahrbuch fur Mineralogie, Vol. 194, 2, pp. 165-173.
Russia, Kola Peninsula
deposit - Kovdor
Abstract: Isolueshite, a cubic complex oxide with the formula NaNbO3, occurs as euhedral crystals 0.4 - 0.7 mm in size in calcite carbonatite, Kovdor ultrabasic-alkaline complex (Kola, Russia). Average composition of isolueshite, based on 40 analyses by wavelength-dispersive electron microprobe is (Na0.84Ca0.07Sr0.01La0.01Ce0.01)S0.95(Nb0.90Ti0.11)S1.01O3. Minor and trace elements are Ti (4.1- 6.8 wt.% TiO2), REEs (1.8 - 4.0 wt.% REE2O3), Ca (1.7- 3.3 wt.% CaO), Zr (0.1- 0.8 wt.% ZrO2), Sr (0.3 - 0.4 wt.% SrO), Th (0.1- 0.5 wt.% ThO2), Fe (0.1- 0.2 wt.% Fe2O3) and Ta (0.1 wt.% Ta2O5). The crystal structure of isolueshite was refined to an agreement index (R1) of 0.028 for 82 unique reflections with |F0| = 4 s(F). The mineral is cubic, Pm3-m, a = 3.9045(5) Å and V = 59.525(13) Å3. The diffraction pattern of the crystal contains only regular and strong Bragg reflections with no signs of diffuse scattering. There are two sites in the crystal structure: A is 12-coordinated (A-O = 2.556(3) Å) and located at the corners of the cubic primitive cell and B is situated in the center of the unit-cell and has an octahedral coordination. The crystal-chemical formula based on the structure refinement is (Na0.84(1)Ca0.16(1))(Nb0.88(1)Ti0.12(1))O3. We suggest that isolueshite is a quenched (kinetically favored) polymorph of lueshite that formed as a result of rapid crystallization due to the sudden drop in temperature and/or pressure.
Reguir, E.P., Chakhmouradian, A.R., Zaitsev, A.N., Yang, P.
Trace element variations and zoning in phlogopite from carbonatites and phoscorites.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 8-9.
carbonatites
Abstract: Phlogopite from carbonatites and phoscorites worldwide shows three major types of core-to-rim trends of compositional variation: Ba+Al-, Fe and Fe+Al enrichment. These major-element trends are accompanied by largely consistent changes in traceelement abundances. Uptake of Rb, Sr, Ba, Sc, V, Mn and HFSE by phlogopite is susceptible to changes in the availability of these elements due to precipitation of other early silicate and oxide phases (especially, magnetite, apatite and niobates). In rare cases, more complex oscillatory and sector patterns are juxtaposed over the principal evolutionary trend, indicating kinetic and crystal-chemical controls over element uptake. Phlogopite is a common accessory to major constituent of carbonatites and genetically related rocks (including phoscorites). Major-element variations of phlogopite from these rocks have been addressed in much detail in the literature (for references, see Reguir et al. 2009), whereas its trace-element characteristics and zoning patterns have so far received little attention. In this work, we examined the compositional variation of phlogopite from 23 carbonatite and phoscorite localities worldwide. The major-element compositions were determined using wavelength-dispersive X-ray spectrometry (WDS) and trace-element abundances by laser-ablation inductively-coupled-plasma mass-spectrometry (LA-ICPMS). Previously, two major core-to-rim zoning trends have been identified in micas from calcite carbonatites (Reguir et al. 2009, 2010). Phlogopite from Oka (Canada) and Iron Hill (USA), for example, involves an increase in kinoshitalite component rim-ward, accompanied by enrichment in high-field-strength elements (HFSE = Zr, Nb, Ta), Sr and Sc. At most other carbonatite localities (e.g., Kovdor in Russia, or Prairie Lake in Canada), phlogopite crystals exhibit rim-ward enrichment in Fe. In the present work, we confirmed these two common types of zoning, and identified new patterns that have not been reported in the previous literature. In addition to the common Fe-enrichment trend, which occurs in both carbonatites (e.g., Guli in Russia and Sokli in Finland) and phoscorites (e.g., Aley in Canada), we identified a Fe-Al-enrichment subtype of this zoning pattern observed, for example, in samples from the Shiaxiondong calcite carbonatite (China). Overall, the Fe-enrichment pattern is accompanied by rim-ward depletion in Ba, Rb and HFSE, coupled with enrichment in Mn. Other trace elements exhibit no consistent variation among the studied samples. The Shiaxiondong material is characterized by the highest recorded Rb values, ranging from 1120 to 660 ppm. Phlogopite from the Kovdor calcite-forsterite-magnetite phoscorite contains the highest recorded levels of Nb and Ta, ranging from 320 ppm and 40 ppm, respectively, in the core to 85 ppm and 4 ppm in the rim. The maximum levels of Zr (up to 50 ppm) were observed in the core of Prairie Lake phlogopite, whereas its rim contains the highest measured Mn content (up to 4100 ppm). The levels of Sc are typically below 100 ppm in samples from calcite and dolomite carbonatites, but may reach 280 ppm in phoscorites. Interestingly, phlogopite from phoscorites shows rim-ward enrichment in Sc, whereas the opposite trend is observed in carbonatitic micas. Phlogopite from calcite carbonatites at Zibo (China) and Valentine Township (Canada), and from phoscorites at Aley (Canada) shows an unusual zoning pattern involving depletion in Fe, which is accompanied by a decrease in Al, Ba, Sr, Zr, Hf, Y, Sc and V abundances. The concentrations of other trace elements, including Nb and Ta show inconsistent variations. In the Aley phoscorite, phlogopite is enriched in Ba (up to 15000 ppm in the core and < 7500 ppm in the rim), but poor in Sr (80 and 35 ppm in the core and rim, respectively) relative to those from the Zibo and Valentine carbonatites. Zirconium levels reach 200 and 170 ppm in the core, and drop to < 40 and 60 ppm in the rim of the Valentine and Zibo samples, respectively. In the Aley sample, the content of Zr does not exceed 55 ppm. The Zibo sample is also enriched in V (up to 230 and 160 ppm in the core and rim, respectively) relative to the two other samples (< 100 ppm V). The Sc and Hf levels are consistently low (less than 30 and 4 ppm, respectively). In addition to simple core-rim patterns, phlogopite from carbonatites and phoscorites may exhibit oscillatory zoning, which involves periodic variations in Fe/Mg ratio. Iron-rich zones are relatively depleted in Mn, but enriched in Nb. One sample of phoscoritic phlogopite (Aley) exhibits striking sector zoning juxtaposed over the overall Feenrichment trend and Fe-Mg oscillations. In terms of major elements, basal sectors perpendicular to [001] are enriched in Fe and Al, but depleted in Mg and K relative to the flank sectors. This enrichment is accompanied by higher Ba, Sr and HFSE levels in the basal sector. Our data confirm that there is no universal pattern of zoning in carbonatitic or phoscoritic phlogopite, and variations in the content of most trace elements are strongly coupled to major-element patterns. Three major core-to-rim variation trends, as well as juxtaposed oscillatory and sector patterns, can be recognized. The observed compositional variations indicate that, in the majority of cases, the trace-element composition of phlogopite is controlled by partitioning of Rb, Sr, Ba, Sc, V, Mn and HFSE between this mineral, its parental magma, and co-precipitating early phases. Among the latter, magnetite, apatite and niobates appear to exert the greatest influence on element distributions. More complex oscillatory and sector patterns imply the presence of kinetic and crystal-chemical controls over element uptake in certain carbonatitic systems
Mineralogical Society Series, isbn 0-903056-22-4 on sale approx 20lbs
Russia, Kola Peninsula
Book - volcanology
Abstract: The first response to the title of this book is often 'What is a phoscorite?'. The exact definition and characteristics of phoscorite are discussed in some detail in Chapter 2 and were the subject of varying opinions amongst the authors of this and other chapters. We nicknamed the book 'the dark side of carbonatites', which covers it nicely. Phoscorites are dark, often very handsome, sometimes economically valuable, magnetite-apatite-silicate rocks, almost always associated with carbonatite. They are key to understanding the longstanding question of how carbonate and carbonate-bearing magmas rise to the crust and the Earth's surface. Despite this, they have been given little attention; a search on geological literature databases will produce thousands of references to carbonatite (up to 4125 on Georef) but not more than thirty references to phoscorite. This book goes some way to redress this balance. Over the last ten years many European and North American scientists have studied Kola rocks in collaboration with Russian colleagues. The idea for this book came from one such project funded by the European organisation, INTAS (Grant No 97-0722). The Kola Peninsula, Russia, is one of the outstanding areas in the World for the concentration and economic importance of alkaline rocks. However, Russian work on the Kola complexes is still relatively
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Experiments on titanosilicates ( lamprophyllite group minerals and lomonosvite) melting: phase relations and petrological significance for Lovozero massif.
Peralk-Carb 2011, workshop held Tubingen Germany June 16-18, Poster
Preservation model for Kola alkaline province for Paleozoic and Paleoproterozoic alkaline magmatism volume comparing.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 13.
Russia, Kola Peninsula
carbonatites
Abstract: Northern part of the Fennoscandian Shield in Kola Peninsula and Northern Karelia was intruded by alkaline magmatic complexes during the two main episodes. Paleoproterozoic alkaline province consisting from five alkaline massifs and Paleozoic alkaline province, consisting from twenty alkaline-ultramafic rock complexes, together with two giant nepheline syenite complexes are practically overlap. Based on the data about morphology and internal structure of the Paleozoic alkaline and ultramaficcarbonatite intrusions and their average denudation rates, the model of alkaline province destruction was developed. This model allows forecasting, how many intrusions of Kola Paleozoic alkaline province will remain and calculate preservation ratio for any moment of future. The dependence of preservation ratio on the age of province allow to compare the initial numbers of massifs in alkaline provinces and conclude that Paleoproterozoic event of alkaline magmatism in Kola peninsula was even more powerful than Paleozoic one.
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 Strange Lake peralkaline complex is one of the world's largest deposits of yttrium, heavy rare-earth elements, and zirconium. The Precambrian intrusive body of peralkaline granitic rocks in central Labrador is extensively mineralized but mineralogically complex. It is a pleasure to acknowledge John Jambor's important contributions to the understanding of the unusual and varied mineralization. He was first to identify and characterize the potentially economic minerals: gittinsite, widespread at Strange Lake but otherwise an uncommon zirconosilicate, and the unusual acid-soluble zircon, which are the main sources of Strange Lake zirconium. He also identified the previously unknown mineral gerenite-(Y), and provided better characterization of kainosite-(Y) and of the complex gadolinite-datolite species which, collectively, account for most of the yttrium and heavy rare-earths. In all, his identification and characterization of these minerals were invaluable to understanding of the peralkaline complex, particularly the late-stage alteration that affected it and generated its economically important minerals, making them amenable to effective metallurgical processes.
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.
Contributions to Mineralogy and Petrology, Vol. 169, 18p.
Africa, Tanzania
Carbonatite
Abstract: We have reconstructed the compositional evolution of the silicate and carbonate melt, and various crystalline phases in the subvolcanic reservoir of Kerimasi Volcano in the East African Rift. Trace element concentrations of silicate and carbonate melt inclusions trapped in nepheline, apatite and magnetite from plutonic afrikandite (clinopyroxene-nepheline-perovskite-magnetite-melilite rock) and calciocarbonatite (calcite-apatite-magnetite-perovskite-monticellite-phlogopite rock) show that liquid immiscibility occurred during the generation of carbonatite magmas from a CO2-rich melilite-nephelinite magma formed at relatively high temperatures (1,100 °C). This carbonatite magma is notably more calcic and less alkaline than that occurring at Oldoinyo Lengai. The CaO-rich (32-41 wt%) nature and alkali-"poor" (at least 7-10 wt% Na2O + K2O) nature of these high-temperature (>1,000 °C) carbonate melts result from strong partitioning of Ca (relative to Mg, Fe and Mn) in the immiscible carbonate and the CaO-rich nature (12-17 wt%) of its silicate parent (e.g., melilite-nephelinite). Evolution of the Kerimasi carbonate magma can result in the formation of natrocarbonatite melts with similar composition to those of Oldoinyo Lengai, but with pronounced depletion in REE and HFSE elements. We suggest that this compositional difference results from the different initial parental magmas, e.g., melilite-nephelinite at Kerimasi and a nephelinite at Oldoinyo Lengai. The difference in parental magma composition led to a significant difference in the fractionating mineral phase assemblage and the element partitioning systematics upon silicate-carbonate melt immiscibility. LA-ICP-MS analysis of coeval silicate and carbonate melt inclusions provides an opportunity to infer carbonate melt/silicate melt partition coefficients for a wide range of elements. These data show that Li, Na, Pb, Ca, Sr, Ba, B, all REE (except Sc), U, V, Nb, Ta, P, Mo, W and S are partitioned into the carbonate melt, whereas Mg, Mn, Fe, Co, Cu, Zn, Al, Sc, Ti, Hf and Zr are partitioned into the silicate melt. Potassium and Rb show no preferential partitioning. Kerimasi melt inclusions show that the immiscible calcic carbonate melt is strongly enriched in Sr, Ba, Pb, LREE, P, W, Mo and S relative to other trace elements. Comparison of our data with experimental results indicates that preferential partitioning of oxidized sulfur (as SO4 2-), Ca and P (as PO4 3-) into the carbonate melt may promote the partitioning of Nb, Ta, Pb and all REE, excluding Sc, into this phase. Therefore, it is suggested that P and S enrichment in calcic carbonate magmas promotes the genesis of REE-rich carbonatites by liquid immiscibility. Our study shows that changes in the partition coefficients of elements between minerals and the coexisting melts along the liquid line of descent are rather significant at Kerimasi. This is why, in addition to the REE, Nb, Ta and Zr are also enriched in Kerimasi calciocarbonatites. We consider significant amounts of apatite and perovskite precipitated from melilite-nephelinite-derived carbonate melt as igneous minerals can have high LREE, Nb and Zr contents relative to other carbonatite minerals.
Geochimica et Cosmochimica Acta, Vol. 198, pp. 70-91.
Mantle
Subduction
Abstract: The equilibrium between aqueous fluids and allanite-bearing eclogite has been investigated to constrain the effect of temperature (T) and fluid composition on the stability of allanite and on the mobility of major and trace elements during the dehydration of eclogites. The experiments were performed at 590-800 °C and 2.4-2.6 GPa, and fluids were sampled as synthetic fluid inclusions in quartz using an improved entrapment technique. The concentrations and bulk partition coefficients were determined for a range of major (Mg, Ca, Na, Fe, Al, Ti) and 16 trace elements as a function of T and fluid composition. The results reveal a significant effect of T on element partitioning between the fluids and the solid mineral assemblage. The partition coefficients increase by more than an order of magnitude for most of the major and trace elements, and several orders of magnitude for light rare-earth elements (LREE) from 590 to 800 °C. The addition of various ligand species into the fluid at 700 °C results in distinctive trends on element partitioning. The concentrations and corresponding partition coefficients of most of the elements are enhanced upon addition of NaF to the fluid. In contrast, NaCl displays a nearly opposite effect by suppressing the solubilities of major elements and consequently affecting the mobility of trace elements that form stable complexes with alkali-(alumino)-silicate clusters in the fluid, e.g. high field strength elements (HFSE). The results further suggest that fluids in equilibrium with orthopyroxene and/or diopsidic clinopyroxene are peralkaline (ASI ~0.1-0.7), whereas fluids in equilibrium with omphacitic pyroxene are more peraluminous (ASI ~1.15). Therefore, natural aqueous fluids in equilibrium with eclogite at about 90 km depth will be slightly peraluminous in composition. Another important finding of this study is the relatively high capacity of aqueous fluids to mobilize LREE, which may be even higher than that of hydrous melts.
Geochemistry International, Vol. 57, 9, pp. 1000-1007.
Mantle
diamond genesis
Abstract: The peritectic reaction of ringwoodite (Mg,Fe)2SiO4 and silicate-carbonate melt with formation of magnesiowustite (Fe,Mg)O, stishovite SiO2, and Mg, Na, Ca, K-carbonates is revealed by experimental study at 20 GPa of phase relations in the multicomponent diamond-forming MgO-FeO-SiO2-Na2CO3-CaCO3-K2CO3 system of the Earth mantle transition zone. An interaction of CaCO3 and SiO2 with a formation of Ca-perovskite CaSiO3 is also detected. It is shown that the peritectic reaction of ringwoodite and melt with the formation of stishovite controls physicochemically the fractional ultrabasic-basic evolution of both magmatic and diamond-forming systems of deep horizons of the transition zone up to its boundary with the Earth lower mantle.
Geochimica et Cosmochimica Acta, Vol. 232, pp. 82-100.
Mantle
geochemistry
Abstract: We have analyzed ancient atmospheric gases trapped in fluid inclusions contained in minerals of Archean (3.3?Ga) to Paleozoic (404?Ma) rocks in an attempt to document the evolution of the elemental composition and isotopic signature of the atmosphere with time. Doing so, we aimed at understanding how physical and chemical processes acted over geological time to shape the modern atmosphere. Modern atmospheric xenon is enriched in heavy isotopes by 30-40‰ u-1 relative to Solar or Chondritic xenon. Previous studies demonstrated that, 3.3?Ga ago, atmospheric xenon was isotopically fractionated (enriched in the light isotopes) relative to the modern atmosphere, by 12.9?±?1.2 (1s) ‰ u-1, whereas krypton was isotopically identical to modern atmospheric Kr. Details about the specific and progressive isotopic fractionation of Xe during the Archean, originally proposed by Pujol et al. (2011), are now well established by this work. Xe isotope fractionation has evolved from 21‰ u-1 at 3.5?Ga to 12.9‰ u-1 at 3.3?Ga. The current dataset provides some evidence for stabilization of the Xe fractionation between 3.3 and 2.7?Ga. However, further studies will be needed to confirm this observation. After 2.7?Ga, the composition kept evolving and reach the modern-like atmospheric Xe composition at around 2.1?Ga ago. Xenon may be the second atmospheric element, after sulfur, to show a secular isotope evolution during the Archean that ended shortly after the Archean-Proterozoic transition. Fractionation of xenon indicates that xenon escaped from Earth, probably as an ion, and that Xe escape stopped when the atmosphere became oxygen-rich. We speculate that the Xe escape was enabled by a vigorous hydrogen escape on the early anoxic Earth. Organic hazes, scavenging isotopically heavy Xe, could also have played a role in the evolution of atmospheric Xe. For 3.3?Ga-old samples, Ar-N2 correlations are consistent with a partial pressure of nitrogen (pN2) in the Archean atmosphere similar to, or lower than, the modern one, thus requiring other processes than a high pN2 to keep the Earth's surface warm despite a fainter Sun. The nitrogen isotope composition of the atmosphere at 3.3?Ga was already modern-like, attesting to inefficient nitrogen escape to space since that time.
Characteristics of the distribution of trace elements in Rocks of the diamond bearing suite of the Chistyakovo Snezhnaya trough of the DonetsBasin.(Russian)
Dopov. Akad. Nauk UKR. RSR Ser. B., Geokl. Khim. Biol., (Russian), No. 3, pp. 5-8
Abstract: Mechanisms of Precambrian orogeny and their contribution to the origin of ultrahigh temperature granulites, granite-greenstone terranes and net crustal growth remain debatable. Here, we use 2D numerical models with 150 °C higher mantle temperatures compared to present day conditions to investigate physical and petrological controls of Precambrian orogeny during forced continental plates convergence. Numerical experiments show that convergence between two relatively thin blocks of continental lithosphere with fertile mantle creates a short-lived cold collisional belt that later becomes absorbed by a long-lived thick and flat ultra-hot accretionary orogen with Moho temperatures of 700-1100 °C. The orogen underlain by hot partially molten depleted asthenospheric mantle spreads with plate tectonic rates towards the incoming lithospheric block. The accretionary orogeny is driven by delamination of incoming lithospheric mantle with attached mafic lower crust and invasion of the hot partially molten asthenospheric wedge under the accreted crust. A very fast convective cell forms atop the subducting slab, in which hot asthenospheric mantle rises against the motion of the slab and transports heat towards the moving orogenic front. Juvenile crustal growth during the orogeny is accompanied by net crustal loss due to the lower crust subduction. Stability of an ultra-hot orogeny is critically dependent on the presence of relatively thin and warm continental lithosphere with thin crust and dense fertile mantle roots subjected to plate convergence. Increased thickness of the continental crust and subcontinental lithospheric mantle, pronounced buoyancy of the lithospheric roots, and decreased mantle and continental Moho temperature favor colder and more collision-like orogenic styles with thick crust, reduced magmatic activity, lowered metamorphic temperatures, and decreased degree of crustal modification. Our numerical modeling results thus indicate that different types of orogens (cold, mixed-hot and ultra-hot) could be created at the same time in the Early Earth, depending on compositional and thermal structures of interacting continental blocks.
Abstract: On contemporary Earth, subduction recycles mafic oceanic crust and associated volatile elements, creating new silicic continental crust in volcanic arcs. However, if the mantle was hotter in the Precambrian, the style of subduction, the depth of devolatilization and the formation of silicic continental crust may have been different. Consequently, the generation of the tonalite-trondhjemite-granodiorite (TTG) suite, which is characteristic of Archean crust, may not have been related to subduction. Here, we use a two-dimensional numerical magmatic-thermomechanical model to investigate intraoceanic subduction for contemporary mantle conditions and at higher mantle temperatures, as appropriate to the Precambrian. In each case, we characterize the thermal structure of the subducting plate and investigate magma compositions and production rates. We use these results to assess the potential growth of silicic continental crust associated with intraoceanic subduction at different mantle temperatures. For the Precambrian, in a set of experiments with ?T?=?150?K and decreasing subducting plate velocity, we find that the contemporary style of subduction was preceded by an arc-free regime dominated by rapid trench rollback and vigorous upwelling of asthenospheric mantle into the space created above the retreating slab. In this regime, formation of magmas by fluid-fluxed melting of the mantle is suppressed. Instead, decompression melting of upwelling asthenospheric mantle results in the widespread development of voluminous plateau-like basaltic magmas. In addition, retreating subduction at higher mantle temperature causes faster descent of the downgoing slab, leads to colder thermal gradients, similar to those associated with active subduction in the western Pacific today, and suppresses melting of the basaltic crust, limiting production of silicic (adakite-like) magmas. With increasing maturity of the subduction system, retreat of the subducting plate ceases, the role of decompression melting strongly decreases and fluid-fluxed melting of the mantle coupled with melting of the hydrated slab begins to produce basaltic and felsic arc volcanic rocks similar to those formed during contemporary subduction. In an additional series of individual experiments at various ?T, an increase of the mantle temperature above ?T?=?150?K leads to episodic and short-lived subduction accompanied by limited production of silicic continental crust. The results of our experimental study demonstrate that a hotter mantle in the Precambrian changes dramatically both the slab dynamics and the processes of magma generation and crustal growth associated with intraoceanic subduction zones. These changes may preclude growth of the early Precambrian silicic continental crust by processes that were dominantly similar to those associated with contemporary subduction.
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.
Journal of Geophysical Research, Vol. 123, 7, pp. 5644-5660.
Africa, east Africa
geophysics - seismic
Abstract: Although the East African rift system formed in cratonic lithosphere above a large-scale mantle upwelling, some sectors have voluminous magmatism, while others have isolated, small-volume eruptive centers. We conduct teleseismic shear wave splitting analyses on data from 5 lake-bottom seismometers and 67 land stations in the Tanganyika-Rukwa-Malawi rift zone, including the Rungwe Volcanic Province (RVP), and from 5 seismometers in the Kivu rift and Virunga Volcanic Province, to evaluate rift-perpendicular strain, rift-parallel melt intrusion, and regional flow models for seismic anisotropy patterns beneath the largely amagmatic Western rift. Observations from 684 SKS and 305 SKKS phases reveal consistent patterns. Within the Malawi rift south of the RVP, fast splitting directions are oriented northeast with average delays of ~1 s. Directions rotate to N-S and NNW north of the volcanic province within the reactivated Mesozoic Rukwa and southern Tanganyika rifts. Delay times are largest (~1.25 s) within the Virunga Volcanic Province. Our work combined with earlier studies shows that SKS-splitting is rift parallel within Western rift magmatic provinces, with a larger percentage of null measurements than in amagmatic areas. The spatial variations in direction and amount of splitting from our results and those of earlier Western rift studies suggest that mantle flow is deflected by the deeply rooted cratons. The resulting flow complexity, and likely stagnation beneath the Rungwe province, may explain the ca. 17 Myr of localized magmatism in the weakly stretched RVP, and it argues against interpretations of a uniform anisotropic layer caused by large-scale asthenospheric flow or passive rifting.
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.
Nuclear Instruments and Methods in Physics Research Section A., A785, pp. 9-13.
Technology
Methodology
Abstract: A new technology for diamond detection in kimberlite based on the tagged neutron method is proposed. The results of experimental researches on irradiation of kimberlite samples with 14.1-MeV tagged neutrons are discussed. The source of the tagged neutron flux is a portable neutron generator with a built-in 64-pixel silicon alpha-detector with double-sided stripped readout. Characteristic gamma rays resulting from inelastic neutron scattering on nuclei of elements included in the composition of kimberlite are registered by six gamma-detectors based on BGO crystals. The criterion for diamond presence in kimberlite is an increased carbon concentration within a certain volume of the kimberlite sample.
Abstract: Our discovery of moissanite grains in a peralkaline syenite from the Água de Pau Volcano (São Miguel, Azores Islands, Portugal) represents the first report of this mineral in present day oceanic geodynamic settings. Raman spectroscopy and single-crystal X-ray diffraction show the presence of both the 6H and 4H polytypes with the predominance of the first one. The distribution of trace elements is homogeneous, except for Al and V. Azorean moissanite often hosts rounded inclusions of metallic Si and other not yet identified metallic alloys. A process involving a flushing of CH4-H2 ultra-reducing fluids in the alkaline melts might be considered as a possible mechanism leading to the formation of natural SiC, thus calling for strongly reducing conditions that were locally met in the crust-mantle beneath the São Miguel Island.
Eakin, C.M., Long, M.D., Scire, A., Beck, S.L., Wagner, L.S., Zandt, G., Tavera, H.
Internal deformation of the subducted Nazca slab inferred from seismic anisotropy. ..new study suggests that the Earth's rigid tectonic plates stay strong when they slide under another plate, known as subduction, may not be universal.
Journal of Geophysical Research: Solid Earth, Vol. 125, e2019JB017884.
Mantle, South America
subduction
Abstract: Nazca subduction beneath South America is one of our best modern examples of long-lived ocean-continent subduction on the planet, serving as a foundation for our understanding of subduction processes. Within that framework, persistent heterogeneities at a range of scales in both the South America and Nazca plates is difficult to reconcile without detailed knowledge of the subducted Nazca slab structure. Here we use teleseismic travel time residuals from >1,000 broadband and short-period seismic stations across South America in a single tomographic inversion to produce the highest-resolution contiguous P wave tomography model of the subducting slab and surrounding mantle beneath South America to date. Our model reveals a continuous trench-parallel fast seismic velocity anomaly across the majority of South America that is consistent with the subducting Nazca slab. The imaged anomaly indicates a number of robust features of the subducted slab, including variable slab dip, extensive lower mantle penetration, slab stagnation in the lower mantle, and variable slab amplitude, that are incorporated into a new, comprehensive model of the geometry of the Nazca slab surface to ~1,100 km depth. Lower mantle slab penetration along the entire margin suggests that lower mantle slab anchoring is insufficient to explain along strike upper plate variability while slab stagnation in the lower mantle indicates that the 1,000 km discontinuity is dominant beneath South America.
Abstract: Mantle xenoliths hosted in Cenozoic alkaline rocks of northern Madagascar (Massif d'Ambre and Bobaomby volcanic fields) are spinel lherzolites, harzburgites and rare websterites. Petrography, electron microprobe, LA-ICP-MS and thermal ionization mass spectrometry techniques allowed to recognize domains characterized by variable degree of partial melting and extent of re-enrichment processes: 1) refractory spinel-to-spinel + plagioclase-lherzolites, with clinopyroxenes having marked LREE (Light Rare Earth Elements) depletion ((La/Yb)N ~ 0.2) and very high 143Nd/144Nd (0.513594), which represent a limited and shallow portion of old mantle that suffered low degree partial melting (2–3%) and was later accreted to the lithosphere. These lherzolites acted as a low-porosity region, being, in places, percolated by small volumes of melts shortly before eruption; 2) lherzolites and harzburgites that suffered variable degrees of partial melt extraction (up to 15%), assisted and/or followed by pervasive, porous flow infiltration of alkaline melts in a relatively large porosity region, leading to the creation of a wide area rich in secondary mineral phases (i.e. olivine, clinopyroxene and pargasitic amphibole), enriched in incompatible elements (e.g., LaN/YbN in clinopyroxene up to 15) and having radiogenic Sr and unradiogenic Nd; 3) websterites and wehrlite-bearing samples that record differentiation processes of alkaline melts highly enriched in Th, U and LREE, not yet documented in the erupted volcanics of northern Madagascar. The mantle xenoliths of northern Madagascar show a regional decrease of the equilibration temperature from to SW (up to 1180 °C, Nosy Be Archipelago) to the NE (up to 900 °C, Bobaomby district). A significant lithologic and geochemical variation of the shallow lithospheric mantle beneath northern Madagascar is noted, in contrast with the relatively uniform geochemical and isotopic composition of the host alkali basalt and basanite lavas.
Earth and Planetary Science Letters, Vol. 478, pp. 52-58.
Canada, Quebec
Mistastin crater
Abstract: Bolide impacts influence primordial evolution of planetary bodies because they can cause instantaneous melting and vaporization of both crust and impactors. Temperatures reached by impact-generated silicate melts are unknown because meteorite impacts are ephemeral, and established mineral and rock thermometers have limited temperature ranges. Consequently, impact melt temperatures in global bombardment models of the early Earth and Moon are poorly constrained, and may not accurately predict the survival, stabilization, geochemical evolution and cooling of early crustal materials. Here we show geological evidence for the transformation of zircon to cubic zirconia plus silica in impact melt from the 28 km diameter Mistastin Lake crater, Canada, which requires super-heating in excess of 2370?°C. This new temperature determination is the highest recorded from any crustal rock. Our phase heritage approach extends the thermometry range for impact melts by several hundred degrees, more closely bridging the gap between nature and theory. Profusion of >2370?°C superheated impact melt during high intensity bombardment of Hadean Earth likely facilitated consumption of early-formed crustal rocks and minerals, widespread volatilization of various species, including hydrates, and formation of dry, rigid, refractory crust.
Abstract: Synthetic diamonds have inspired much interest for their unique photophysical properties and versatile potential applications, but their phosphorescent phenomenon and mechanism have been paid much less attention. Here, phosphorescent diamonds with a lifetime of 5.4?s were synthesized by high-pressure and high-temperature method, and the diamonds exhibit an emission band at around 468?nm under the excitation wavelength of 230?nm. The quantum yield of the phosphorescent diamonds is about 4.7% at ambient temperature and atmosphere, which is the first report on the quantum yield of diamonds. The unique phosphorescence emission can be attributed to the radiative recombination from iron related donors and boron related acceptors.
Abstract: Preliminary mineralogical and geochemical studies have been carried out on dolomite marble drill cores from the Bayan Obo REE deposit in China. Three types of apatites and four types of monazites have been identified based on textural features: Type 1 apatite occurs as grains with minor monazite (Type 1 monazite) on its border; Type 2 apatite veinlet shows clusters of assemblages with abundant bastnäsite and parisite at the rim; Type 3 apatite has a linear array associated with fluorite and bastnäsite veinlets. Type 2 monazite occurs as clusters intergrowing with parisite and fluorite. Type 3 and 4 monazites occur as polymineralic (fluorite and bastnäsite) and monomineralic veinlets, respectively. These four types of monazites have similar LREE composition but variable Y content (Y2O3 ranging from below determination limits to 0.7?wt%). The three types of apatites also show different REE content and distribution patterns, ranging from high REE abundance (?REE?+?Y: 27243-251789?ppm) and strong LREE enrichment [(La/Yb)CN ~101] in Type 1, less LREE enrichment [(La/Yb)CN ~8] in Type 2 to relatively low REE abundance (?REE?+?Y: 4323-11175?ppm) but high REE fractionation [(La/Yb)CN ~58] in Type 3. The primary apatite has high Sr (5461-6892?ppm) and REE content, implying a carbonatite origin. The late-stage apatites (Types 2 and 3) show different Sr and REE abundances. Significant differences in their Sr composition (6189?±?573, 6041?±?549 and 3492?±?802 for Types 1-3 samples, respectively) and Y/Ho ratio (20.9?±?0.11, 19.5?±?0.17 and 17.4?±?0.37, respectively) indicate that the three types of apatites may have crystallized from different metasomatic fluids. Multi-stage metasomatism resulted in remobilization and redeposition of primary REE minerals to form the Bayan Obo REE deposit.
Abstract: Our discovery of moissanite grains in a peralkaline syenite from the Água de Pau Volcano (São Miguel, Azores Islands, Portugal) represents the first report of this mineral in present day oceanic geodynamic settings. Raman spectroscopy and single-crystal X-ray diffraction show the presence of both the 6H and 4H polytypes with the predominance of the first one. The distribution of trace elements is homogeneous, except for Al and V. Azorean moissanite often hosts rounded inclusions of metallic Si and other not yet identified metallic alloys. A process involving a flushing of CH4-H2 ultra-reducing fluids in the alkaline melts might be considered as a possible mechanism leading to the formation of natural SiC, thus calling for strongly reducing conditions that were locally met in the crust-mantle beneath the São Miguel Island.
Abstract: Our discovery of moissanite grains in a peralkaline syenite from the Água de Pau Volcano (São Miguel, Azores Islands, Portugal) represents the first report of this mineral in present day oceanic geodynamic settings. Raman spectroscopy and single-crystal X-ray diffraction show the presence of both the 6H and 4H polytypes with the predominance of the first one. The distribution of trace elements is homogeneous, except for Al and V. Azorean moissanite often hosts rounded inclusions of metallic Si and other not yet identified metallic alloys. A process involving a flushing of CH4-H2 ultra-reducing fluids in the alkaline melts might be considered as a possible mechanism leading to the formation of natural SiC, thus calling for strongly reducing conditions that were locally met in the crust-mantle beneath the São Miguel Island.
Abstract: Two-station surface-wave analysis was used to measure Rayleigh-wave phase velocities between 105 station pairs in western Canada, straddling the boundary between the tectonically active Cordillera and the adjacent stable craton. Major variations in phase velocity are seen across the boundary at periods from 15 to 200 s, periods primarily sensitive to upper mantle structure. Tomographic inversion of these phase velocities was used to generate phase velocity maps at these periods, indicating a sharp contrast between low-velocity Cordilleran upper mantle and high-velocity cratonic lithosphere. Depth inversion along selected transects indicates that the Cordillera-craton upper mantle contact varies in dip along the deformation front, with cratonic lithosphere of the Taltson province overthrusting Cordilleran asthenosphere in the northern Cordillera, and Cordilleran asthenosphere overthrusting Wopmay lithosphere further south. Localized high-velocity features at sub-lithospheric depths beneath the Cordillera are interpreted as Farallon slab fragments, with the gap between these features indicating a slab window. A high-velocity feature in the lower lithosphere of the Slave province may be related to Proterozic or Archean subduction.
Abstract: Carbonatite is a magmatic rock with high carbonate and low silicate contents, which mostly originate in the mantle. It is therefore of critical importance to understand the behavior of carbon in the mantle, and consequently deep carbon recycling. However, the formation of carbonatite is largely unresolved. In particular, the source of carbonatite the carbonate remains obscure. Previous studies showed that the solidus of carbonated mantle peridotite was lower than the Earth’s geotherm in the Archean and the Early Proterozoic era, before ~1.4 Ga ago. Therefore, the mantle should have been severely decarbonated early in Earth’s history. This is consistent with the low carbon abundance in the asthenospheric mantle (~100 ppm), as indicated by low carbonate concentrations in mid-ocean ridge basalts. Consequently, carbonate in young mantle must have been mostly obtained in the post-Archean era by two processes. These are either oxidation of diamond in the mantle or recycling of sedimentary carbonates through plate subduction. Here we show that the Sr and Nd isotope variations in carbonatite may be plausibly explained by mixing of three endmembers, (1) recycled sedimentary carbonates, (2) depleted mantle, and (3) a low Sr and Nd isotopes endmember. The low Sr, Nd carbonate reservoirs for carbonatites of different ages plot roughly on the evolution line of the primitive mantle, suggesting that they were successively released from a well-preserved, non-carbonate mantle source. The preferred candidate for this endmember is carbonate formed through oxidation of diamond by ferric ion released through decomposition of bridgmanite, which is carried up from the lower mantle via background upwelling, compensational to the volume of oceanic slabs penetrating into the lower mantle1.
Lower crustal xenoliths from Jurassic kimberlite diatremes, Upper Michigan USA: evidence for Proterozoic orogenesis and plume magmatism in the lower crust of the southern Superior Province.
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.
Galimov, E., Kudin, A., Skorobogatskii, V., Plotnichenko, V., Bondarev, O., Zarubin, B., Strazdovskii, V., Aronin, A., Fisenko, A., Bykov, I., Barinov, A.
Experimental corrobation of the synthesis of diamond in the cavitation process.
Doklady Physical Chemistry, Vol. 49, 3, pp. 150-153.
Boletin del Museo Nacional de Historia Narural del Paraguay, Vol. 20, 2, pp. 205-213. pdf available in * Port
South America, Paraguay
Impact Crater
Abstract: We report here the discovery and study of several new modeled large impact craters in Eastern Paraguay, South America. They were studied by geophysical information (gravimetry, magnetism), field geology and also by microscopic petrography. Clear evidences of shock metamorphic effects were found (e.g., diaplectic glasses, PF, PDF in quartz and feldspar) at 4 of the modeled craters: 1) Negla: diameter:~80-81 km., 2) Yasuka Renda D:~96 km., 3) Tapyta, D: ~80 km. and 4) San Miguel, D: 130-136 km. 5) Curuguaty, D: ~110 km. was detected and studied only by geophysical information. Target-rocks range goes from the crystalline Archaic basement to Permian sediments. The modeled craters were in some cases cut by tholeiitic/alkaline rocks of Mesozoic age and partially covered by lavas of the basaltic Mesozoic flows (Negla, Yasuka Renda, Tapyta and Curuguaty). One of them was covered in part by sediments of Grupo Caacupé (age: Silurian/Devonian). Some of these modeled craters show gold, diamonds, uranium and REE mineral deposits associated. All new modeled large impact craters are partially to markedly eroded.
Argon isotopic ratios and Potassium, Sodium and other trace element contents in Premier and Finsch mine diamonds contents in Premier and Finsch mine diamonds
In: Material Science of the Earth's interiors, Terra Science Publishing, pp. 375-386
Journal of African Earth Sciences, Vol. 113, pp. 35-50.
Africa, Cameroon
Geochemistry
Abstract: Trace element abundances in three indicator minerals (corundum, chrysoberyl, and zircon grains) from the western Mamfe gem placers, as determined by LA-ICP-MS analytical techniques, are shown to be sensitive to their crystallization conditions and source rock types. Corundum is dominantly composed of Al (standardized at 529,300 ppm), Fe (2496-12,899 ppm), and Ti (46-7070 ppm). Among element ratios, Fe/Mg (73-1107), Fe/Ti (0.5-245.0), Ti/Mg (1-175), and Ga/Mg (4-90) are generally higher whereas, Cr/Ga (<0.072) is low. The Fe (=12,899), Ga (=398), Mg (2-62), Cr (1.1-33.0), and V (3.0-93.0) contents (in ppm) mostly typify corundum grains formed in magmatic rocks, although some are metamorphic affiliated. A very higher Ti and significantly low Ga, Ta and Nb contents in some blue grains, suggest interesting concentrations of those high-tech metals in their source rocks. Chrysoberyl is dominantly composed of Al (standardized at 425,000 ppm) and Be (62701-64371 ppm). Iron (7605-9225 ppm), Sn (502-3394 ppm), and Ti (33-2251 ppm) contents are high, whereas Ga (333-608 ppm), Ta (<456.0 ppm), and Nb (<3.0 ppm) are significantly low. The high (Be and Sn) and significantly low Ga-Rb abundances, and Ta > Nb in the western Mamfe chrysoberyls show that they were crystallized in granitic pegmatites, with some of those source rocks being enriched in Ta and Sn. Zirconium oxide (ZrO2: standardized at 66.1 wt.%)) is the only major oxide in analysed coarse-grained zircons. Within the minor elementary suites: Hf (4576-12,565 ppm) and Y (48-2805 ppm) contents are significantly high. The trace element suites include: Th (7-1565 ppm), U (13-687 ppm), and ?REE (50-2161 ppm), whose values are significantly low. The (Yb/Sm)N, Ce/Ce*, and Eu/Eu* anomalies range from 1.0 to 227.0, 0 to 308, and 0.08 to 1.7 respectively. They are Hf-Y-HREE enriched and depleted zircons mainly crystallized in magmatic oxidized environments. They were mainly sorted from granitoids, syenites and kimberlites.
A new manifestation of micro-diamonds in metamorphic rocks as an evidence of the regional character of high-pressure metamorphism in KokchetavMassif.(in Russian)
Doklady Academy of Sciences Akademy Nauk SSSR, (Russian), Vol. 321, No. 1, pp. 189-193. # HB124
Vendian Early Ordovician geodynamic evolution and model for exhumation of ultrahigh and high pressure rocks from the Kokchetav subduction collision zone.
Russian Geology and Geophysics, Vol. 47, 4, pp. 424-440.
Abstract: Coalingite, Mg10Fe2(CO3)(OH)24 • 2H2O, rare Mg -Fe hydrous carbonate, has been found in the course of the mineralogical study of a disintegrated kimberlite breccia from the Manchary pipe of the Khompu -May field located in the Tamma Basin, Central Yakutia, 100 km south of Yakutsk. Coalingite occurs as small reddish brown platelets, up to 0.2 mm in size. It is associated with lizardite, chrysotile and brucite, which are typical kimberlitic assemblage. Coalingite is a supergene mineral, but in this case, it is produced by the interaction of brucite-bearing kimberlite and underground water circulating through a vertical or oblique fault zone.
Abstract: Experimental studies in the Fe3C-SiO2-MgO system (P = 6.3 GPa, T = 1100-1500°C, t = 20-40 h) have been carried out. It has been established that carbide-oxide interaction resulted in the formation of Fe-orthopyroxene, graphite, wustite, and cohenite (1100 and 1200°C), as well as a Fe-C-O melt (1300-1500°C). The main processes occurring in the system at 1100 and 1200°C are the oxidation of cohenite, the extraction of carbon from carbide, and the crystallization of metastable graphite, as well as the formation of ferrosilicates. At T = 1300°C, graphite crystallization and diamond growth occur as a result of the redox interaction of a predominantly metallic melt (Fe-C-O) with oxides and silicates. The carbide-oxide interaction studied can be considered as the basis for modeling a number of carbon-producing processes in the lithospheric mantle at fO2 values near the iron-wustite buffer.
Contents of trace elements in olivines from diamonds and peridotite xenoliths of the V.Grib kimberlite pipe ( Arkhangel'sk Diamondiferous province, Russia).
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
The deep carbon cycle: new evidence from superdeep diamonds.
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
Zedgenizov, D., Rubatto, D., Shatsky, V., Ragozin, A., Kalinina, V.
Eclogitic diamonds from variable crustal protoliths in the northeastern Siberian Craton: trace elements and coupled Delta13C-delta 180 signatures in diamonds and garnet inclusions.
Abstract: Microinclusions of high-density fluids (HDF's) occur in cloudy diamonds from the Mir and Internatsionalnaya kimberlite pipes (Malobotuobia kimberlite field, Siberian platform). These HDFs are of typical high-Mg carbonatitic composition; a few diamonds contain microinclusions that define a low-Mg carbonatitic to silicic trend. The observed variations are interpreted as resulted from mixing of two contrasting fluids derived from the partial melting mainly of carbonated peridotite (the high-Mg carbonatitic HDFs) and eclogite (silica-rich HDFs and HDFs with high Ca/(Ca + Mg + Fe)). Immiscibility of carbonatitic and silica-rich fluids provides a possible mechanism for the co-existence of the observed HDFs but needs further proof. The uniform carbon isotope composition of cloudy diamonds with high-Mg carbonatitic microinclusions from both kimberlite pipes implies a single peridotitic source.
Abstract: The Zarnitsa kimberlite pipe is one of the largest pipes of the Yakutian diamondiferous province. Currently, some limited published data exists on the diamonds from this deposit. Among the diamond population of this pipe there is a specific series of dark gray to black diamonds with transition morphologies between octahedron and rounded rhombic dodecahedron. These diamonds have specific zonal and sectorial mosaic-block internal structures. The inner parts of these crystals have polycrystalline structure with significant misorientations between sub-individuals. The high consistency of the mechanical admixtures (inclusions) in the diamonds cores can cause a high grid stress of the crystal structure and promote the block (polycrystalline) structure of the core components. These diamond crystals have subsequently been formed due to crystallization of bigger sub-individuals on the polycrystalline cores according to the geometric selection law.
Abstract: Yellow cuboid diamonds are commonly found in diamondiferous alluvial placers of the Northeastern Siberian platform. The internal structure of these diamonds have been studied by optical microscopy, X-Ray topography (XRT) and electron backscatter diffraction (EBSD) techniques. Most of these crystals have typical resorption features and do not preserve primary growth morphology. The resorption leads to an evolution from an originally cubic shape to a rounded tetrahexahedroid. Specific fibrous or columnar internal structure of yellow cuboid diamonds has been revealed. Most of them are strongly deformed. Misorientations of the crystal lattice, found in the samples, may be caused by strains from their fibrous growth or/and post-growth plastic deformation.
Abstract: Cuboid diamonds are particularly common in the placers of the northeastern Siberian platform, but their origin remains unclear. These crystals usually range in color from dark yellow to orange and, more interestingly, are characterized by unusual low aggregated nitrogen impurities (non-aggregated C-center), suggesting a short residence time and/or low temperatures at which they have been stored in the mantle. In order to track possible isotopic signature that could help deciphering cuboid diamond’s crystallization processes, d¹³C values, d¹5N values, and nitrogen concentrations have been determined in situ in three samples using secondary ion mass spectrometry (SIMS), whereas nitrogen aggregation states have been determined by FTIR spectroscopy. The samples fall out of the d¹³C vs. d¹5N field of canonical mantle composition. Different scales of carbon and nitrogen fractionation may produce the observed variations. Alternatively, mixing mantle and crustal material would obscure initial co-variations of d¹³C values with d¹5N or nitrogen content.
Abstract: The microinclusions in cuboid diamonds from Ebelyakh River deposits (northeastern Siberian craton) have been investigated by FIB/TEM techniques. It was found that these microinclusions have multiphase associations, containing silicates, oxides, carbonates, halides, sulfides, graphite, and fluid phases. The bulk chemical composition of the microinclusions indicates two contrasting growth media: Mg-rich carbonatitic and Al-rich silicic. Each media has their own specific set of daughter phases. Carbonatitic microinclusions are characterized by the presence of dolomite, phlogopite, apatite, Mg, Fe-oxide, KCl, rutile, magnetite, Fe-sulfides, and hydrous fluid phases. Silicic microinclusions are composed mainly of free SiO2 phase (quartz), high-Si mica (phengite), Al-silicate (paragonite), F-apatite, Ca-carbonates enriched with Sr and Ba, Fe-sulfides, and hydrous fluid phases. These associations resulted from the cooling of diamond-forming carbonatitic and silicic fluids/melts preserved in microinclusions in cuboid diamonds during their ascent to the surface. The observed compositional variations indicate different origins and evolutions of these fluids/melts.
Abstract: New findings of silicate-melt inclusions in two alluvial diamonds (from the Kholomolokh placer, northeastern Siberian Platform) are reported. Both diamonds exhibit a high degree of N aggregation state (60-70% B) suggesting their long residence in the mantle. Raman spectral analysis revealed that the composite inclusions consist of clinopyroxene and silicate glass. Hopper crystals of clinopyroxene were observed using scanning electron microscopy and energy-dispersive spectroscopic analyses; these are different in composition from the omphacite inclusions that co-exist in the same diamonds. The glasses in these inclusions contain relatively high SiO2, Al2O3, Na2O and, K2O. These composite inclusions are primary melt that partially crystallised at the cooling stage. Hopper crystals of clinopyroxene imply rapid cooling rates, likely related to the uplift of crystals in the kimberlite melt. The reconstructed composition of such primary melts suggests that they were formed as the product of metasomatised mantle. One of the most likely source of melts/fluids metasomatising the mantle could be a subducted slab.
Abstract: 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.
Abstract: Much of our knowledge of the Earth’s deep interior comes from theoretical models, which are based on the results of experimental petrology and seismology. Diamonds in such models are the unique natural samples because they contain and preserve inclusions of mantle materials that have been entrapped during diamond growth and remained unchanged for long geologic time. In the present study for superdeep sublithospheric diamonds from Saõ-Luiz (Juina, Brazil) and northeastern Siberian Platform with mineral inclusions of the Transition Zone and Lower Mantle (majorite garnet, coesite (stishovite), ferropericlase and Mg-Si-, Ca-Si-, Ca-Ti, Ca-Si- Ti-perovskite), the diffraction of backscattered electrons technique (EBSD) revealed features of the internal structure. Superdeep diamonds are characterized by a defective and imperfect internal structure, which is associated with the processes of growth and post-growth plastic deformation. The deformation is manifested both in the form of stripes parallel to the (111) direction, and in the form of an unordered disorientation of crystal blocks up to 2°. In addition, for many crystals, a block structure was established with a greater disorientation of the sub-individuals, as well as the presence of “diamond-in-diamond” inclusions and microtwins. Additional stresses are often observed around inclusions associated with the high remaining internal pressure. It has previously been shown that the crystal structure of superdeep diamonds is significantly deformed around inclusions of perovskites, SiO2 (stishovite?), and Mg2SiO4 (ringwoodite?). The significant plastic deformations detected by the EBSD around inclusions testify to phase transitions in superdeep minerals (perovskites, stishovite, and ringwoodite) [1].
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.
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.
Some specific features of genesis of microdiamonds of octahedral and cubic habit from kimberlites of the Udachanaya pipe inferred from carbon isotopes - defect
Russian Geology and Geophysics, Vol. 48, pp. 299-304.
Zedgenizov, D.A., Kagi, H., Shatsky, V.S., Ragozin, A.
Local variations of carbon isotope composition in diamonds from Sao-Luis ( Brazil): evidence for heterogenous carbon reservoir in sublithospheric mantle.
Multiple growth events in diamonds with cloudy Micro inclusions from the Mir kimberlite pipe: evidence from the systematics of optically active defects.
Russian Geology and Geophysics, Vol. 56, 1, pp. 330-343.
Diamondiferous subcontinental lithospheric mantle of the northeastern Siberian Craton: evidence from mineral inclusions in alluvial diamonds. Kapchan Fold Belt Olenek Province
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.
Bulletin of the Russian Academy of Sciences. Physics ** IN ENG, Vol. 80, 1, pp. 74-77.
South America, Brazil
Diamond formation
Abstract: Luminescence kinetics in the temperature range of 80 480 K and the red region of the spectrum is studied for Brazilian diamonds. Components with decay time constants of 23 and 83 ns are observed at room temperature after being excited by laser radiation with wavelengths of 375 and 532 nm, which differs considerably from the data published earlier for the luminescence kinetics of NV 0- and NV -centers.
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 specific gray to almost black diamonds of rounded morphology are especially typical in alluvial placers of the northeastern part of the Siberian platform. The results of study of internal structure of these diamonds are presented. X-ray topography and birefringence patterns of polished plates of studied diamonds show their radial mosaic structure. Diamonds consists of slightly misorientated (up to 20') subindividuals which are combined to mosaic wedge-shaped sectors. Electron back-scatter diffraction technique has demonstrated that subindividuals are often combined in the single large blocks (subgrains). The whole crystals commonly consist of several large subgrains misoriented up to 5° to one another. The total nitrogen content of these diamonds vary in the range 900-3300 ppm and nitrogen aggregation state (NB/(NB + NA)*100) from 25 to 64 %. Rounded diamond crystals of variety V are suggested to have been formed at the high growth rate caused by the high oversaturation of carbon in the crystallization medium. It may result in the splitting of growing crystal and their radial mosaic structure as a sequence. High content of structural nitrogen defects and the great number of mechanical impurities - various mineral and fluid inclusions may also favor to generation of this structure.
Abstract: Polycrystalline diamond aggregates (boart, framesites, diamondites) have been widely studied but their origin is poorly understood. We report the results of a study in situ of two polished fragments of fine-grained (40-400 µm size of individual diamond grains) dense polycrystalline diamond aggregates from the Mir pipe containing visible multiple interstitial garnet inclusions. They were analyzed for major and trace elements of inclusions and one of them — for d13C and N abundance and isotopic composition of host diamonds. These aggregates are classified as variety IX by Orlov (1977). No cavities were observed in these samples. Sixty two irregular garnet grains and one clinopyroxene inclusion were detected and analyzed in sample Mr 832. Garnets are homogeneous within single grains but variable in Mg# [100Mg/(Mg + Fe)] from 60 up to 87 and CaO contents (3.3-5.3 wt.%) among grains with a trend to negative correlation. Low Cr (550-640 ppm) confirms eclogitic (E-type) paragenesis. High Na2O contents (5.2 wt.%) of a single pyroxene inclusion are additional evidence of eclogitic nature of this sample. Wide variations in trace elements (ppm) are characteristic for garnet grains: Sr (2.7-25.6), Y (9.7-14.1), Zr (15.6-38.7) and positive Eu anomaly is present. The d13C of diamonds within studied sample is variable (- 6.4 ÷- 9.8 ‰) as well as N abundance (75-1150 ppm) and d15N - 27, - 38, - 58 ‰. The second peridotitic (U/P-type) sample Mr 838 contains eight inclusions of Mg-rich Cr-pyropes (Mg# ~ 85, Cr2O3 3.2-3.4 wt.%) and magnesite inclusion with 4.35 wt.% FeO and 1.73 wt.% CaO. Trace element content in pyropes is relatively uniform (ppm): Sr (0.4-1.6), Y (13.2-13.4) and Zr (13.0). We conclude that heterogeneous distribution of the trace elements among garnet grains in Mr 832 and magnesite presence in Mr 838 are indicative of the effects of mantle metasomatism and rapid crystallization shortly before the eruption of the kimberlite.
Geochemistry International, Vol. 54, 10, pp. 834-838.
South America, Brazil
Deposit - Sao Luiz
Abstract: We report cloudy micro- and nano-inclusions in a superdeep diamond from São-Luiz, Brazil which contains inclusions of ferropericlase (Mg, Fe)O and former bridgmanite (Mg, Fe)SiO3 and ringwoodite (Mg, Fe)2SiO4. Field emission-SEM and TEM observations showed that the cloudy inclusions were composed of euhedral micro-inclusions with grain sizes ranging from tens nanometers to submicrometers. Infrared absorption spectra of the cloudy inclusions showed that water, carbonate, and silicates were not major components of these micro- and nano-inclusions and suggested that the main constituent of the inclusions was infrared-inactive. Some inclusions were suggested to contain material with lower atomic numbers than that of carbon. Mineral phase of nano- and micro-inclusions is unclear at present. Microbeam X-ray fluorescence analysis clarified that the micro-inclusions contained transition metals (Cr, Mn, Fe, Co, Ni, Cu, Zn) possibly as metallic or sulfide phases. The cloudy inclusions provide an important information on the growth environment of superdeep diamonds in the transition zone or the lower mantle.
Doklady Earth Sciences, Vol. 470, 2, pp. 1059-1062.
Russia
Deposit - Internationalskaya
Abstract: The staged high-pressure annealing of natural cubic diamonds with numerous melt microinclusions from the Internatsional’naya kimberlite pipe was studied experimentally. The results mainly show that the carbonate phases, the daughter phases in partially crystallized microinclusions in diamonds, may undergo phase transformations under the mantle P-T conditions. Most likely, partial melting and further dissolution of dolomite in the carbonate-silicate melt (homogenization of inclusions) occur in inclusions. The experimental data on the staged high-pressure annealing of diamonds with melt microinclusions allow us to estimate the temperature of their homogenization as 1400-1500°C. Thus, cubic diamonds from the Internatsional’naya pipe could have been formed under quite high temperatures corresponding to the lithosphere/asthenosphere boundary. However, it should be noted that the effect of selective capture of inclusions with partial loss of volatiles in relation to the composition of the crystallization medium is not excluded during the growth. This may increase the temperature of their homogenization significantly between 1400 and 1500°C.
Abstract: Alluvial placers of the northeastern Siberian Platform are characterized by a specific diamond population: regular cuboids, forming a continuous color series from yellowish-green to yellow and dark orange. This is the first comprehensive study of a large number of cuboid diamonds focusing on their morphology, N content and aggregation state, photoluminescence, C isotopic composition and inclusions. The cuboids are cubic (i.e. nearly flat faced) to subrounded crystals; most of them are resorbed. The cathodolominescence images and the birefringence patterns show that many cuboid diamonds record deformation. The cuboid diamonds are characterized by unusual FTIR spectra with the presence of C- (single nitrogen atom) and A- (pair of neighbour nitrogen atoms) centers, and two centers of unknown origin, termed X and Y. The presence of single substitutional nitrogen defects (C centers) in all cuboid diamonds testifies either storage in the mantle at relatively cool conditions or formation just prior to eruption of their host kimberlites. The studied diamonds are also characterized by the presence of specific set of luminescence centers: N3, H3, S1, NVo and NV-, some of which are suggested to have formed during deformation subsequent to diamond growth. The cuboid diamonds show a wide range of carbon isotope compositions from mantle-like values towards strongly 13C depleted compositions (- 6.1 to - 20.2‰ d13C). Combined with the finding of an eclogitic sulfide inclusion, the light carbon isotope compositions link the formation of the studied cuboids to deeply subducted basic protoliths, i.e. former oceanic crust.
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.
Abstract: Notable within-crystal variability of mineralogical and geochemical properties of single natural diamonds are commonly attributed to changing chemistry of parental fluids, sources of carbon and redox conditions of diamond precipitation. A distinct type of compositional heterogeneity (mixed-habit structure) is well-known to occur in diamonds as well as in many other minerals due to purely “structural” reasons that are unequal crystal chemistry of crystallographically different faces and selective absorption and fractionation of impurities between adjacent growth pyramids. Based on the combined cathodoluminescence, Fourier-transformed infrared spectroscopy and photoluminescence spectroscopy, study of nine diamond crystals with different growth histories and external morphology, but all showing mixed-habit patterns at different growth stages, we show that mixed-diamonds may grow in closed system conditions or with a slowly decreasing growth rate from a media with a much lower impurity content than previously thought. Intracrystal nitrogen distribution seems to be a function of growth rate even in the cases of unusual impurity partitioning between growth sectors. Generally poor with IR-active hydrogen at moderate nitrogen aggregation parameters, studied diamonds likely resemble the low hydrogen content from the growth medium that, for cubic diamonds, was typically suggested hydrogen-rich and a crucial factor for growth of cubic and mixed-habit diamonds. We also show that mixed-habit diamond growth may occur not only in peridotitic suite but also in an extended field of geochemical affinities from high-Ni to low-Ni or maybe even Ni-free environments, such as pyroxenitic or eclogitic.
Physics and Chemistry of Minerals, Vol. 44, 9, pp. 655-667.
Russia, Yakutia
deposit - Mir
Abstract: In this study, the specific features of structural defects of type IaB diamonds from the Mir kimberlite pipe (Yakutian diamondiferous province) have been characterized using FTIR and photoluminescence spectroscopy. Mineral inclusions in these diamonds [olivine (Ol), orthopyroxene (OPx), chromite (Chr), sulphide (Sf)] correspond to associations of peridotite rocks at the base of the lithosphere. Nitrogen content in type IaB diamonds shows significant variations, suggesting different growth media and/or several growth stages. A specific feature of these diamonds is the absence or very small amount of platelets, which may be related to annealing during their long-term residence at the temperatures of the base of the lithosphere. All studied diamonds show the presence of hydrogen defects that are active in IR spectra with an intense line at 3107 cm-1, and additional weaker lines at 3085 and 3237 cm-1, which correlated with high nitrogen content. Type IaB diamonds are also characterized by the presence of nitrogen-nickel luminescence centres S2, S3 and 523.2 nm. This feature distinguishes them from superdeep diamonds with extreme nitrogen aggregation states, which clearly attest to different growth conditions and crystallization media of type IaB diamonds from the Mir kimberlite pipe.
Geochemistry International, Vol. 55, 12, pp. 1193-1203.
Russia
diamond - crystallography
Abstract: In this paper, we consider an ontogenic model for the formation of morphological types of growth and dissolution of cubic diamonds of variety II by Yu.L. Orlov from placers of the Anabar diamondiferous region. The following ontogenic domains of crystals and corresponding evolutionary stages of growth accompanying a general decrease in supersaturation in the crystallization medium were distinguished: microblock mosaic cuboids with defects produced by the mechanism of rotational plastic deformation-cuboids with linear translation deformations-cuboids and antiskeletal growth forms of cuboids composed of octahedral growth layers-pseudocubic growth forms of a flat-faced octahedron. The crystal morphological evolution of cuboids during the bulk dissolution of individuals in fluid-bearing melt transporting them to the surface was traced. The investigation of transitional forms of cuboid diamond dissolution showed that the final form of diamond dissolution is a rounded tetrahexahedroid independent of the combination of cuboid faces with subordinate faces of octahedron, rhombododecahedron, and tetrahexahedron observed on resorbed crystals of cubic habit. It was found that the final stages of cuboid dissolution produced disk-shaped microrelief features on the diamond surface in the form of randomly distributed ideal rounded etch pits resulting from interaction with microscopic cavitation gas bubbles released during the decompression of ascending kimberlite melt.
Russian Geology and Geophysics, Vol. 59, pp. 486-498.
Russia
deposit - Zarnitsa
Abstract: Mosaic diamonds from the Zarnitsa kimberlite (Daldyn field, Yakutian diamondiferous province) are morphologicaly and structurally similar to dark gray mosaic diamonds of varieties V and VII found frequently in placers of the northeastern Siberian craton. However, although being similar in microstructure, the two groups of diamonds differ in formation mechanism: splitting of crystals in the case of placer diamonds (V and VII) and growth by geometric selection in the Zarnitsa kimberlite diamonds. Selective growth on originally polycrystalline substrates in the latter has produced radial micro structures with grains coarsening rimward from distinctly polycrystalline cores. Besides the formation mechanisms, diamonds of the two groups differ in origin of mineral inclusions, distribution of defects and nitrogen impurity, and carbon isotope composition. Unlike the placer diamonds of varieties V and VII, the analyzed crystals from the Zarnitsa kimberlite enclose peridotitic minerals (olivines and subcalcic Cr-bearing pyropes) and have total nitrogen contents common to natural kimberlitic diamonds (0 to 1761 ppm) and typical mantle carbon isotope compositions (-1.9 to -6.2%c 513C; -4.2%c on average). The distribution of defect centers in the Zarnitsa diamond samples fits the annealing model implying that nitrogen aggregation decreases from core to rim.
Abstract: Melt/fluid inclusions in diamonds provide important evidence for mantle diamond-forming fluids or melts. By now, the major characteristics of the composition of microinclusions have been analyzed in diamonds from several kimberlite provinces and pipes worldwide [1-4]. Here we report the first data on the composition of parent diamondforming melts for diamonds from the Arkhangelsk kimberlite province. After the study of morphology, specialty of the internal structure, and distribution of microinclusions in diamonds, 10 single crystals were selected from the 31 diamonds of the representative collection. The studied crystals may be divided into two groups: cuboids and coated diamonds. The crystals have grayish yellow or dark gray colors and are almost nontransparent due to the high content of microinclusions. Polished slices of these diamonds were studied by IR-spectroscopy, which allowed us to calculate the content of nitrogen defects, as well as the content of water and carbonates in microinclusions. X-ray spectral analyses allowed to study the composition of fluid/melt microinclusions and showed that they were essentially carbonate-silicate with significant variations between these two end-members. All inclusions contain water, with the highest H2O/CO2 in highly siliceous inclusions. Unlike diamonds from Canada and South Africa [1, 2], the studied inclusions in diamionds from the Arkhangelsk province are almost free of chlorides. Comparison of the data obtained with the database on fliud/melt inclusions in diamonds worldwide shows similar of Arkhangelsk diamonds to some diamonds from Yakutia [3, 4], and the data obtained are the most similar to the composition of microinclusions in diamonds from the Internatsionalnaya pipe (Yakutia).
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.
Contributions to Mineralogy and Petrology, Vol. 173, 16p. Doi.org/10.1007/s00410-018-1513-y
Russia
deposit - Udachnaya
Abstract: A xenolith of bimineralic eclogite from the Udachnaya kimberlite pipe provides a snapshot of interaction between mantle rocks and diamond-forming fluids/melts. The major-element composition of the eclogite is similar to that of N-MORB and/or oceanic gabbros, but its trace-element pattern shows the effects of mantle metasomatism, which resulted in diamond formation. The diamonds are clustered in alteration veins that crosscut primary garnet and clinopyroxene. The diamonds contain microinclusions of a fluid/melt dominated by carbonate and KCl. Compared to the worldwide dataset, the microinclusions in these diamonds fall in middle of the range between saline fluids and low-Mg carbonatitic melts. The fluid/melt acted as a metasomatic agent that percolated through ancient eclogitic rocks stored in the mantle. This interaction is consistent with calculated partition coefficients between the rock-forming minerals and diamond-forming fluid/melt, which are similar to experimentally-determined values. Some differences between the calculated and experimental values may be due to the low contents of water and silicates in the chloride-carbonate melt observed in this study, and in particular its high contents of K and LILE. The lack of nitrogen aggregation in the diamonds implies that the diamond-forming metasomatism took place shortly before the eruption of the kimberlite, and that the microinclusions thus represent saline carbonate-rich fluids circulating in the basement of lithospheric mantle (150-170 km depth).
Ivanov, A.V., Mukasa, S.B., Kamenetsky, V.S., Ackerson, M., Zedgenizov, D.A.
Volatile concentrations in olivine hosted melt inclusions from meimechite and melanephenelinite lavas of the Siberian Trap Large Igneous Province: evidence for flux related high Ti, high Mg magmatism.
Mineralogy and Petrology, 10.1007/s0710-019-00661-3
Russia
diamond morphology
Abstract: Five typical coated diamonds (from Udachnaya, Yubileynaya, and Aikhal kimberlite pipes) with untypically low microinclusion abundances and four monocrystalline diamonds (Udachnaya, Mir, Nyurbinskaya pipes) that exhibit thin intermediate microinclusion-bearing zones were examined in details for growth structures, characteristic infrared absorption and photoluminescence, and composition of microinclusions. The internal structures of diamonds of both types imply that fluid inclusions entrapment in diamonds does not necessarily relate to the terminal stage of rapid fibrous growth. Instead, nitrogen aggregation state in some diamonds showed that both fibrous coats and inclusion-bearing layers might experience an annealing during mantle residence long enough to pre-date the ultimate kimberlite eruption, whereas the diamonds with internal inclusion-bearing zones also experienced later protracted history of monocrystalline growth. The presence of chloride-carbonate-silicate fluids/melts in monocrystalline diamonds indicate their generation from media generally similar to that observed in some fibrous diamonds. However, the composition of these metasomatizing fluids is different for the mantle beneath Udachnaya (mostly carbonatitic) and other pipes (Aikhal, Yubileynaya, Mir; variable abundance of silicic high-density fluids). The abundance of silica-rich fluids record either a heterogeneous distribution of eclogites in the subcontinental lithospheric mantle, or the operation of silica-rich slab-derived fluids. The inclusion abundance as well as the type of growth (fibrous or monocrystalline) is considered to be controlled by the volume of fluid fluxes; in this case, fluid consumption leads to decreasing growth rates, diminishing inclusion entrainment and stability of layered octahedrons. The detected minor compositional variations of high-density fluids in these diamonds may be due to local scale thermal perturbation in the host source and/or limited chemical heterogeneity of the parental fluid. The high amount of chlorides in high-density fluids from monocrystalline diamonds provide a new evidence for compositions of fluids/melts acting as primary metasomatic agent in the deep mantle of Siberian craton.
Abstract: Five typical coated diamonds (from Udachnaya, Yubileynaya, and Aikhal kimberlite pipes) with untypically low microinclusion abundances and four monocrystalline diamonds (Udachnaya, Mir, Nyurbinskaya pipes) that exhibit thin intermediate microinclusion-bearing zones were examined in details for growth structures, characteristic infrared absorption and photoluminescence, and composition of microinclusions. The internal structures of diamonds of both types imply that fluid inclusions entrapment in diamonds does not necessarily relate to the terminal stage of rapid fibrous growth. Instead, nitrogen aggregation state in some diamonds showed that both fibrous coats and inclusion-bearing layers might experience an annealing during mantle residence long enough to pre-date the ultimate kimberlite eruption, whereas the diamonds with internal inclusion-bearing zones also experienced later protracted history of monocrystalline growth. The presence of chloride-carbonate-silicate fluids/melts in monocrystalline diamonds indicate their generation from media generally similar to that observed in some fibrous diamonds. However, the composition of these metasomatizing fluids is different for the mantle beneath Udachnaya (mostly carbonatitic) and other pipes (Aikhal, Yubileynaya, Mir; variable abundance of silicic high-density fluids). The abundance of silica-rich fluids record either a heterogeneous distribution of eclogites in the subcontinental lithospheric mantle, or the operation of silica-rich slab-derived fluids. The inclusion abundance as well as the type of growth (fibrous or monocrystalline) is considered to be controlled by the volume of fluid fluxes; in this case, fluid consumption leads to decreasing growth rates, diminishing inclusion entrainment and stability of layered octahedrons. The detected minor compositional variations of high-density fluids in these diamonds may be due to local scale thermal perturbation in the host source and/or limited chemical heterogeneity of the parental fluid. The high amount of chlorides in high-density fluids from monocrystalline diamonds provide a new evidence for compositions of fluids/melts acting as primary metasomatic agent in the deep mantle of Siberian craton.
Geochemistry International, Vol. 57, 9, pp. 963-980.
Russia
deposit - Lomonosov
Abstract: The data on the composition of microinclusions in diamonds from the Lomonosov deposits are reported for the first time. The studied diamonds include “coated” (n = 5) and cubic (n = 5) crystals. The estimated range of the degree of nitrogen aggregation in diamonds (4-39% B1) does not support their direct links with kimberlite magmatism; however, their short occurrence in the mantle at higher temperatures is probable as well. The composition of melt/fluid microinclusions in these samples varies from essentially carbonatitic to significantly silicate. It is shown that the contents of MgO, CaO, Na2O, Cl, and P2O5 decrease with increasing content of silicates and water. Different mechanisms of the generation and evolution of diamond-forming media are discussed to explain the observed variations.
Geochemistry International, Vol. 57, 9, pp. 964-972.
Mantle
diamond inclusions
Abstract: The paper describes mineralogical characteristics of SiO2 inclusions in sublithospheric diamonds, which typically have complicated growth histories showing alternating episodes of growth, dissolution, and postgrowth deformation and crushing processes. Nitrogen contents in all of the crystals do not exceed 71 ppm, and nitrogen is detected exclusively as B-defects. The carbon isotope composition of the diamonds varies from d13? = -26.5 to -6.7‰. The SiO2 inclusions occur in association with omphacitic clinopyroxenes, majoritic garnets, CaSiO3, jeffbenite, and ferropericlase. All SiO2 inclusions are coesite, which is often associated with micro-blocks of kyanite in the same inclusions. It was suggested that these phases have been produced by the retrograde dissolution of primary Al-stishovite, which is also evidenced by the significant internal stresses in the inclusions and by deformations around them. The oxygen isotope composition of SiO2 inclusions in sublithospheric diamonds (d18O up to 12.9‰) indicates a crustal origin of the protoliths. The negative correlation between the d18O of the SiO2 inclusions and the d13C of their host diamonds reflects interaction processes between slab-derived melts and reduced mantle rocks at depths greater than 270 km.
Abstract: Archean cratons are underlain by highly depleted subcontinental lithospheric mantle (SCLM). However, there are extensive evidences that Archean SCLM has been extensively refertilized by metasomatic processes, with the addition of Fe, Ca, and Al to depleted protoliths. The distribution of sub-calcic Cr-rich garnets in the SCLM beneath the Siberian craton suggests (1) sub-calcic garnets and diamonds are metasomatic phases in the cratonic SCLM; (2) the distribution of both phases is laterally heterogeneous on relatively small scales and related to ancient structural controls [1]. Re-Os isotopic compositions of twenty six sulfide inclusions in lherzolitic Cr-pyropes from Upper Muna kimberlites have been determined by laser ablation MCICPMS. Most analysed sulfides (~92%) have very low Re/Os ratios (<0.07), and their Re-depletion ages (TRD) form three major peaks: 3.4-2.8, 2.2-1.8 and 1.4-1.2 Ga (±0.03 Ga, mean 2s analytical uncertainty). One sulfide give the oldest TRD age at 4 Ga. Our data suggest that refertilization of the highly depleted SCLM and the introduction of Cr-pyrope garnet occurred in several episodes. The oldest age of ca 4 Ga indicate on the beginning of the formation of the depleted SCLM of the Siberian Craton in Hadean time [2].
Physics and Chemistry of Minerals, Vol. 47, 20 doi.org/10/1007/ s00269-020-01088-5 19p. Pdf
Russia
deposit - International
Abstract: New spectroscopic data were obtained to distinguish the specific features of brown and pink diamonds from Internatsionalnaya kimberlite pipe (Siberian craton). It is shown that pink and brown samples differ markedly in the content and degree of aggregation of nitrogen defects. Pink diamonds generally have higher nitrogen content and a lower aggregation state compared to brown samples, which often show significant variations in nitrogen content and aggregation state between different growth zones. The 491 and 576 nm luminescent centres, which are signs of deformed brown diamonds, are absent or of low intensity in pink diamonds implying that high nitrogen content predominantly in A form in the pink diamonds had stiffened the diamonds against natural plastic deformation. The GR1 centre, formed by a neutrally charged vacancy, was observed only in pink diamonds, which may be due to their formation and storage in the mantle at lower-temperature conditions. Mineral inclusions indicate peridotitic and eclogitic paragenesis for studied brown and pink diamonds, respectively. It is suggested that brown diamonds have been formed in a primitive mantle at higher temperatures and/or stored there much longer.
Contributions to Mineralogy and Petrology, Vol. 175, 98 10.1007/s00410-020-01741-w 11p. Pdf
Russia, Yakutia
diamond crystallography
Abstract: The 35 paired diamond intergrowths of rounded colorless transparent and gray opaque crystals from the placers of northeastern Siberian Platform were investigated. Mineral inclusions (KFsp, Coe, E-Grt, Po) detected in studied samples belong to eclogitic paragenesis. The majority of studied samples have uniform ranges of nitrogen content (1126-1982 at. ppm) and carbon isotope composition (-?16.8 to -?23.2 ‰). These characteristics pointing towards subducted material are possible sources for their genesis. Two samples consist of a gray opaque crystal with the subduction-related characteristics (d13C ca. -?21‰ and N ca. 1300 at. ppm) and a transparent crystal with low nitrogen content (412 and 29 at. ppm) and a heavy carbon isotopic composition (d13C -?4.2 and -?4.6‰) common for primary mantle range. The higher degree of nitrogen aggregation in the crystals with mantle-like characteristics testifies their longer storage in the mantle conditions. These samples reflect multistage diamond growth history and directly indicate the mixing of mantle and subduction carbon sources at the basement of subcontinental lithospheric mantle of northeastern Siberian Platform.
Contributions to Mineralogy and Petrology, Vol. 175, 106, 21p. Pdf
Russia
deposit - Nyurbinskaya
Abstract: We present a new dataset on the composition of high-density fluids (HDFs) in cloudy (n?=?25), coated (n?=?10) and cuboid (n?=?10) diamonds from the Nyurbinskaya kimberlite pipe. These diamonds represent different populations each showing distinct growth histories. The cores of coated diamonds display multiple growth stages and contrasting sources of carbon. Fibrous coats and cuboid diamonds have similar carbon isotopes and nitrogen systematics, suggesting their formation in the last metasomatic events related to kimberlite magmatism, as is common for most such diamonds worldwide. The HDFs in most of these diamonds span a wide range from low-Mg carbonatitic to hydrous silicic compositions. The major- and trace-element variations suggest that the sources for such HDFs range in composition between the depleted mantle and more fertile mantle reservoirs. Hydrous-silicic HDFs could originate from a 13C-enriched source, which originates through subduction of crustal metasedimentary material. Percolation of such HDFs through carbonated eclogites and peridotites facilitates the formation of cuboid diamonds and fibrous coats in the mantle section beneath the corresponding area of the Siberian craton. Cloudy diamonds represent an apparently older population, reflecting continuous diamond formation predominantly from high-Mg carbonatitic HDFs that caused discrete episodes of diamond precipitation. Their high Mg# and enrichment in incompatible elements support a metasomatized peridotitic source for these HDFs.
Minerals MDPI, Vol. 10, 1084, doi:10.3390/ min10121084 10p. Pdf
Mantle
spectroscopy
Abstract: The composition of clinopyroxenes is indicative for chemical and physical properties of mantle substrates. In this study, we present the results of Raman spectroscopy examination of clinopyroxene inclusions in natural diamonds (n = 51) and clinopyroxenes from mantle xenoliths of peridotites and eclogites from kimberlites (n = 28). The chemical composition of studied clinopyroxenes shows wide variations indicating their origin in different mantle lithologies. All clinopyroxenes have intense Raman modes corresponding to metal-oxygen translation (~300-500 cm-1), stretching vibrations of bridging O-Si-Obr (?11~670 cm-1), and nonbridging atoms O-Si-Onbr (?16~1000 cm-1). The peak position of the stretching vibration mode (?11) for the studied clinopyroxenes varies in a wide range (23 cm-1) and generally correlates with their chemical composition and reflects the diopside-jadeite heterovalent isomorphism. These correlations may be used for rough estimation of these compounds using the non-destructive Raman spectroscopy technique.
Archean to Proterzooic crustal evolution in the Central Zone of the Limpopo belt ( South Africa - Botswana ): constraints from combined U Pb and Lu Hf isotope analyses of zircon.
Archean to Proterzooic crustal evolution in the Central Zone of the Limpopo belt ( South Africa - Botswana ): constraints from combined U Pb and Lu Hf isotope analyses of zircon.
U Pb and Lu Hf isotope record of detrital zircon grains from the Limpopo Belt - evidence for crustal recycling at the Hadean to Early Archean transition.
Geochimica et Cosmochimica Acta, Vol. 72, 21, Nov. 1, pp. 5304-5329.
Hafnium isotope record of the Ancient Gneiss Complex, Swaziland, southern Africa: evidence for Archean crust-mantle formation and crust reworking between 3.66 and 2.73 Ga.
Journal of the Geological Society, Vol. 168, pp. 953-964.
Symposium on critical and strategic materials, British Columbia Geological Survey Paper 2015-3, held Nov. 13-14, pp. 69-74.
Canada, Quebec
Alkalic
Abstract: The Crevier alkaline intrusion is in the Grenville Province, north of the Lac Saint-Jean region of Québec (Fig. 1). It covers ~25 km2 (Bergeron, 1980) and intrudes charnockitic suites in the allochthon belt defi ned by Rivers et al. (1989). This intrusion has a U-Pb zircon age of 957.5 ± 2.9 Ma (Groulier et al., 2014) and is oriented N320°, along the axis of crustal weakness known as the Waswanipi-Saguenay corridor (Bernier and Moorhead, 2000). This corridor is related to the Saguenay graben, which hosts the Saint-Honoré (Niobec) Nb-Ta-REE deposit and Montviel REE deposit. The age of the Saint-Honoré carbonatite was estimated at 584 to 650 Ma (K-Ar whole rock; Vallée and Dubuc, 1970; Boily and Gosselin, 2004). The Montviel intrusion has a U-Pb zircon age of 1894 ± 3.5 Ma (David et al., 2006; Goutier, 2006). These crystallization ages are very different and cannot be related to a single event for the injection of alkaline intrusions. As mapped by Bergeron (1980), the Crevier alkaline intrusion is broadly composed of syenite and carbonatite rocks (Fig. 2). The Nb- Ta mineralization consists of pyrochlore hosted by a nepheline syenite dike swarm in the centre of the intrusion. The highest REE concentrations, up to 729 ppm La and 1465 ppm Ce, are at the edge of the Crevier alkaline intrusion (Niotaz sud showing; Fig. 2).
Journal of Asian Earth Sciences, in press available, 17p.
India
geodynamics
Abstract: The Pitepani volcanic suite of the Dongargarh Supergroup, central India comprises of a calc-alkaline suite and a tholeiitic suite, respectively. The rare earth element (REE) patterns, mantle normalized plots and relict clinopyroxene chemistry of the Pitepani calc-alkaline suite are akin to high-Mg andesites (HMA) and reveal remarkable similarity to the Cenozoic Setouchi HMA from Japan. The Pitepani HMAs are geochemically correlated with similar rocks in the Kotri-Dongargarh mobile belt (KDMB) and in the mafic dykes of the Bastar Craton. The rationale behind lithogeochemical correlations are that sanukitic HMAs represent fore-arc volcanism over a very limited period of time, under abnormally high temperature conditions and are excellent regional and tectonic time markers. Furthermore, the tholeiitic suites that are temporally and spatially associated with the HMAs in the KDMB and in the mafic dykes of the Bastar Craton are classified into: (a) a continental back-arc suite that are depleted in incompatible elements, and (b) a continental arc suite that are more depleted in incompatible elements, respectively. The HMA suite, the continental back-arc and continental arc suites are lithogeochemically correlated in the KDMB and in the mafic dykes of the Bastar Craton. The three geochemically distinct Neoarchaean magmatic suites are temporally and spatially related to each other and to an active continental margin. The identification of three active continental margin magmatic suites for the first time, provides a robust conceptual framework to unravel the Neoarchaean geodynamic evolution of the Bastar Craton. We propose an active continental margin along the Neoarchaen KDMB with eastward subduction coupled with slab roll back or preferably, ridge-subduction along the Central Indian Tectonic Zone (CITZ) to account for the three distinct magmatic suites and the Neoarchean geodynamic evolution of the Bastar Craton.
Journal of Asian Earth Sciences, Vol. 157, pp. 218-234.
India
Craton
Abstract: The Pitepani volcanic suite of the Dongargarh Supergroup, central India comprises of a calc-alkaline suite and a tholeiitic suite, respectively. The rare earth element (REE) patterns, mantle normalized plots and relict clinopyroxene chemistry of the Pitepani calc-alkaline suite are akin to high-Mg andesites (HMA) and reveal remarkable similarity to the Cenozoic Setouchi HMA from Japan. The Pitepani HMAs are geochemically correlated with similar rocks in the Kotri-Dongargarh mobile belt (KDMB) and in the mafic dykes of the Bastar Craton. The rationale behind lithogeochemical correlations are that sanukitic HMAs represent fore-arc volcanism over a very limited period of time, under abnormally high temperature conditions and are excellent regional and tectonic time markers. Furthermore, the tholeiitic suites that are temporally and spatially associated with the HMAs in the KDMB and in the mafic dykes of the Bastar Craton are classified into: (a) a continental back-arc suite that are depleted in incompatible elements, and (b) a continental arc suite that are more depleted in incompatible elements, respectively. The HMA suite, the continental back-arc and continental arc suites are lithogeochemically correlated in the KDMB and in the mafic dykes of the Bastar Craton. The three geochemically distinct Neoarchaean magmatic suites are temporally and spatially related to each other and to an active continental margin. The identification of three active continental margin magmatic suites for the first time, provides a robust conceptual framework to unravel the Neoarchaean geodynamic evolution of the Bastar Craton. We propose an active continental margin along the Neoarchaen KDMB with eastward subduction coupled with slab roll back or preferably, ridge-subduction along the Central Indian Tectonic Zone (CITZ) to account for the three distinct magmatic suites and the Neoarchean geodynamic evolution of the Bastar Craton.
Earth Planetary Science Letters, Vol. 490, pp. 100-109.
Canada
craton
Abstract: Cratons are generally considered to comprise lithosphere that has remained tectonically quiescent for billions of years. Direct evidence for stability is mainly founded in the Phanerozoic sedimentary record and low-temperature thermochronology, but for extensive parts of Canada, earlier stability has been inferred due to the lack of an extensive rock record in both time and space. We used 40Ar/39Ar multi-diffusion domain (MDD) analysis of K-feldspar to constrain cratonic thermal histories across an intermediate (~150-350°C) temperature range in an attempt to link published high-temperature geochronology that resolves the timing of orogenesis and metamorphism with lower-temperature data suited for upper-crustal burial and unroofing histories. This work is focused on understanding the transition from Archean-Paleoproterozoic crustal growth to later intervals of stability, and how uninterrupted that record is throughout Earth’s Proterozoic "Middle Age." Intermediate-temperature thermal histories of cratonic rocks at well-constrained localities within the southern Canadian Shield of North America challenge the stability worldview because our data indicate that these rocks were at elevated temperatures in the Proterozoic. Feldspars from granitic rocks collected at the surface cooled at rates of <0.5°C/Ma subsequent to orogenesis, seemingly characteristic of cratonic lithosphere, but modeled thermal histories suggest that at ca. 1.1-1.0 Ga these rocks were still near ~200°C - signaling either reheating, or prolonged residence at mid-crustal depths assuming a normal cratonic geothermal gradient. After 1.0 Ga, the regions we sampled then underwent further cooling such that they were at or near the surface (<< 60°C) in the early Paleozoic. Explaining mid-crustal residence at 1.0 Ga is challenging. A widespread, prolonged reheating history via burial is not supported by stratigraphic information, however assuming a purely monotonic cooling history requires at the very least 5 km of exhumation beginning at ca. 1.0 Ga. A possible explanation may be found in evidence of magmatic underplating that thickened the crust, driving uplift and erosion. The timing of this underplating coincides with Mid-Continent extension, Grenville orogenesis, and assembly of the supercontinent Rodinia. 40Ar/39Ar MDD data demonstrate that this technique can be successfully applied to older rocks and fill in a large observational gap. These data also raise questions about the evolution of cratons during the Proterozoic and the nature of cratonic stability across deep time.
Abstract: Cratons are generally considered to comprise lithosphere that has remained tectonically quiescent for billions of years. Direct evidence for stability is mainly founded in the Phanerozoic sedimentary record and low-temperature thermochronology, but for extensive parts of Canada, earlier stability has been inferred due to the lack of an extensive rock record in both time and space. We used 40Ar/39Ar multi-diffusion domain (MDD) analysis of K-feldspar to constrain cratonic thermal histories across an intermediate (~150-350?°C) temperature range in an attempt to link published high-temperature geochronology that resolves the timing of orogenesis and metamorphism with lower-temperature data suited for upper-crustal burial and unroofing histories. This work is focused on understanding the transition from Archean-Paleoproterozoic crustal growth to later intervals of stability, and how uninterrupted that record is throughout Earth's Proterozoic “Middle Age.” Intermediate-temperature thermal histories of cratonic rocks at well-constrained localities within the southern Canadian Shield of North America challenge the stability worldview because our data indicate that these rocks were at elevated temperatures in the Proterozoic. Feldspars from granitic rocks collected at the surface cooled at rates of <0.5?°C/Ma subsequent to orogenesis, seemingly characteristic of cratonic lithosphere, but modeled thermal histories suggest that at ca. 1.1-1.0 Ga these rocks were still near ~200?°C - signaling either reheating, or prolonged residence at mid-crustal depths assuming a normal cratonic geothermal gradient. After 1.0 Ga, the regions we sampled then underwent further cooling such that they were at or near the surface («60?°C) in the early Paleozoic. Explaining mid-crustal residence at 1.0 Ga is challenging. A widespread, prolonged reheating history via burial is not supported by stratigraphic information, however assuming a purely monotonic cooling history requires at the very least 5 km of exhumation beginning at ca. 1.0 Ga. A possible explanation may be found in evidence of magmatic underplating that thickened the crust, driving uplift and erosion. The timing of this underplating coincides with Mid-Continent extension, Grenville orogenesis, and assembly of the supercontinent Rodinia. 40Ar/39Ar MDD data demonstrate that this technique can be successfully applied to older rocks and fill in a large observational gap. These data also raise questions about the evolution of cratons during the Proterozoic and the nature of cratonic stability across deep time.
Abstract: Heat transfer in the solid Earth drives processes that modify temperatures, leaving behind a clear signature that we can measure using noble gas thermochronology. This allows us to record the thermal histories of rocks and obtain the timing, rate, and magnitude of phenomena such as erosion, deformation, and fluid flow. This is done by measuring the net balance between the accumulation of noble gas atoms from radioactive decay and their loss by temperature-activated diffusion in mineral grains. Together with knowledge about noble gas diffusion in common minerals, we can then use inverse models of this accumulation-diffusion balance to recover thermal histories. This approach is now a mainstream method by which to study geodynamics and Earth evolution.
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: 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: 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.
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 (1s) 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).
Abstract: Magmas forming large igneous provinces (LIP) on continents are generated by extensive melting in the deep crust and underlying mantle and associated with break-up of ancient supercontinents, followed by formation of a new basaltic crust in the mid-oceanic rifts. A lack of the unifying model in understanding the sources of LIP magmatism is justified by lithological and geochemical complexity of erupted magmas on local (e.g. a cross-section) and regional (a single and different LIP) scales. Moreover, the majority of LIP rocks do not fit general criteria for recognizing primary/primitive melts (i.e. < 8 wt% MgO and absence of high-Fo olivine phenocrysts). This study presents the mineralogical (olivine, Cr-spinel, orthopyroxene), geochemical (trace elements and Sr-Nd-Hf-Pb isotopes) and olivine-hosted melt inclusion compositional characteristics of a single primitive (16 wt% MgO), high-Ti (2.5 wt% TiO2) picrite with high-Mg olivine (up to 91 mol% Fo) from the Letaba Formation in the ~ 180 Ma Karoo LIP (south Africa). The olivine compositions (unusually high d18O (6.17‰), high NiO (0.36-0.56 wt%) and low MnO and CaO (0.12-0.20 and 0.12-0.22 wt%, respectively)) are used to argue for a non-peridotitic mantle source. This is supported by the enrichment of the rock and melts in most incompatible trace elements and depletion in heavy rare earth elements (e.g. high Gd/Yb) that reflects residual garnet in the source of melting. The radiogenic isotopes resemble those of the model enriched mantle (EM-1) and further argue for a long-term enrichment of the source in incompatible trace elements. The enriched high-Ti compositions, strongly fractionated incompatible trace elements, presence of primitive olivine and high-Cr spinel in the Letaba picrites are closely matched by olivine-phyric rocks from the ~ 260 Ma Emeishan (Yongsheng area, SW China) and ~ 250 Ma Siberian (Maimecha-Kotuy region, N Siberia) LIPs. However, many other compositional parameters (e.g. trace element and d18O compositions of olivine phenocrysts, Fe2 +/Fe3 + in Cr-spinel, Sr-Nd-Hf isotope ratios) only partially overlap or even diverge. We thus imply that parental melts of enriched picritic rocks with forsteritic olivine from three major continental igneous provinces - Karoo, Emeishan and Siberia cannot be assigned to a common mantle source and similar melting conditions. The Karoo picrites also exhibit some mineralogical and geochemical similarities with rocks and glasses in the south Atlantic Ridge and adjacent fracture zones. The geodynamic reconstructions of the continental plate motions since break-up of the Gondwanaland in the Jurassic support the current position of the source of the Karoo magmatism in the southernmost Atlantic. Co-occurrence of modern and recent anomalous rocks with normal mid-ocean ridge basalts in this region can be related to blocks/rafts of the ancient lithosphere, stranded in the ambient upper mantle and occasionally sampled by rifting-related decompressional melting.
Abstract: Magmas forming large igneous provinces (LIP) on continents are generated by extensive melting in the deep crust and underlying mantle and associated with break-up of ancient supercontinents, followed by formation of a new basaltic crust in the mid-oceanic rifts. A lack of the unifying model in understanding the sources of LIP magmatism is justified by lithological and geochemical complexity of erupted magmas on local (e.g. a cross-section) and regional (a single and different LIP) scales. Moreover, the majority of LIP rocks do not fit general criteria for recognizing primary/primitive melts (i.e. < 8 wt% MgO and absence of high-Fo olivine phenocrysts). This study presents the mineralogical (olivine, Cr-spinel, orthopyroxene), geochemical (trace elements and Sr-Nd-Hf-Pb isotopes) and olivine-hosted melt inclusion compositional characteristics of a single primitive (16 wt% MgO), high-Ti (2.5 wt% TiO2) picrite with high-Mg olivine (up to 91 mol% Fo) from the Letaba Formation in the ~ 180 Ma Karoo LIP (south Africa). The olivine compositions (unusually high d18O (6.17‰), high NiO (0.36–0.56 wt%) and low MnO and CaO (0.12–0.20 and 0.12–0.22 wt%, respectively)) are used to argue for a non-peridotitic mantle source. This is supported by the enrichment of the rock and melts in most incompatible trace elements and depletion in heavy rare earth elements (e.g. high Gd/Yb) that reflects residual garnet in the source of melting. The radiogenic isotopes resemble those of the model enriched mantle (EM-1) and further argue for a long-term enrichment of the source in incompatible trace elements. The enriched high-Ti compositions, strongly fractionated incompatible trace elements, presence of primitive olivine and high-Cr spinel in the Letaba picrites are closely matched by olivine-phyric rocks from the ~ 260 Ma Emeishan (Yongsheng area, SW China) and ~ 250 Ma Siberian (Maimecha-Kotuy region, N Siberia) LIPs. However, many other compositional parameters (e.g. trace element and d18O compositions of olivine phenocrysts, Fe2 +/Fe3 + in Cr-spinel, Sr-Nd-Hf isotope ratios) only partially overlap or even diverge. We thus imply that parental melts of enriched picritic rocks with forsteritic olivine from three major continental igneous provinces – Karoo, Emeishan and Siberia cannot be assigned to a common mantle source and similar melting conditions. The Karoo picrites also exhibit some mineralogical and geochemical similarities with rocks and glasses in the south Atlantic Ridge and adjacent fracture zones. The geodynamic reconstructions of the continental plate motions since break-up of the Gondwanaland in the Jurassic support the current position of the source of the Karoo magmatism in the southernmost Atlantic. Co-occurrence of modern and recent anomalous rocks with normal mid-ocean ridge basalts in this region can be related to blocks/rafts of the ancient lithosphere, stranded in the ambient upper mantle and occasionally sampled by rifting-related decompressional melting.
Journal of Geophysical Research: Solid Earth, Vol. 124, 12, pp. 13124-131249. ( open access)
South America, Venezuela
geophysics - seismic
Abstract: Northwestern Venezuela is located in the complex deformation zone between the Caribbean and South American plates. Several models regarding the lithospheric structure of the Mérida Andes have been proposed. Nevertheless, they lack relevant structural information in order to support the interpretation of deeper structures. Therefore, a 560-km-long refraction profile across the northern part of Mérida Andes, oriented in a NNW direction, covering areas from the Proterozoic basement in the south, to both Paleozoic and Meso-Cenozoic terranes of northwestern Venezuela to the north, is analyzed in this contribution. Thirteen land shots were recorded by 545 short-deployment seismometers, constraining P wave velocity models from first-arrival seismic tomography and layer-based inversion covering the whole crust in detail, with some hints to upper mantle structures. The most prominent features imaged are absence of a crustal root associated to the Mérida Andes, as the Northern Andes profile is located marginal to the Andean crustal domain, and low-angle subduction of the Caribbean oceanic slab (~10-20°) beneath northwestern South America. Further crustal structures identified in the profile are (a) crustal thinning beneath the Falcón Basin along the western extension of the Oca-Ancón fault system interpreted as a back-arc basin; (b) suture zones between both the Proterozoic and Paleozoic provinces (Ouachita-Marathon-related suture?), and Paleozoic and Meso-Cenozoic terranes (peri-Caribbean suture) interpreted from lateral changes in seismic velocity; and (c) evidence of a deep Paleozoic(?) extensional basin, underlying thick Mesozoic and Cenozoic sequences (beneath the Guárico area).
Abstract: An experimental study of the dissolution of natural and synthetic diamonds in a sulfur-bearing iron melt (Fe0.7S0.3) with high P-T parameters (4 GPa, 1400°?) was performed. The results demonstrated that under these conditions, octahedral crystals with flat faces and rounded tetrahexahedral diamond crystals are transformed into rounded octahedroids, which have morphological characteristics similar to those of natural diamonds from kimberlite. It was suggested that, taking into account the complex history of individual natural diamond crystals, including the dissolution stages, sulfur-bearing metal melts up to sulfide melts were not only diamond-forming media during the early evolution of the Earth, but also natural solvents of diamond in the mantle environment before the formation of kimberlitic melts.
Abstract: Yellow cuboid diamonds are commonly found in diamondiferous alluvial placers of the Northeastern Siberian platform. The internal structure of these diamonds have been studied by optical microscopy, X-Ray topography (XRT) and electron backscatter diffraction (EBSD) techniques. Most of these crystals have typical resorption features and do not preserve primary growth morphology. The resorption leads to an evolution from an originally cubic shape to a rounded tetrahexahedroid. Specific fibrous or columnar internal structure of yellow cuboid diamonds has been revealed. Most of them are strongly deformed. Misorientations of the crystal lattice, found in the samples, may be caused by strains from their fibrous growth or/and post-growth plastic deformation.
Contributions to Mineralogy and Petrology, Vol. 175, 98 10.1007/s00410-020-01741-w 11p. Pdf
Russia, Yakutia
diamond crystallography
Abstract: The 35 paired diamond intergrowths of rounded colorless transparent and gray opaque crystals from the placers of northeastern Siberian Platform were investigated. Mineral inclusions (KFsp, Coe, E-Grt, Po) detected in studied samples belong to eclogitic paragenesis. The majority of studied samples have uniform ranges of nitrogen content (1126-1982 at. ppm) and carbon isotope composition (-?16.8 to -?23.2 ‰). These characteristics pointing towards subducted material are possible sources for their genesis. Two samples consist of a gray opaque crystal with the subduction-related characteristics (d13C ca. -?21‰ and N ca. 1300 at. ppm) and a transparent crystal with low nitrogen content (412 and 29 at. ppm) and a heavy carbon isotopic composition (d13C -?4.2 and -?4.6‰) common for primary mantle range. The higher degree of nitrogen aggregation in the crystals with mantle-like characteristics testifies their longer storage in the mantle conditions. These samples reflect multistage diamond growth history and directly indicate the mixing of mantle and subduction carbon sources at the basement of subcontinental lithospheric mantle of northeastern Siberian Platform.
Geochemistry, Geophysics, Geosystems, Vol. 19, 7, pp. 2062-2086. doi.org/10/1029/ 2018GC007534
Mantle
geophysics - seismics
Abstract: Some seismic models derived from tomographic studies indicate elevated shear-wave velocities (=4.7 km/s) around 120-150 km depth in cratonic lithospheric mantle. These velocities are higher than those of cratonic peridotites, even assuming a cold cratonic geotherm (i.e., 35 mW/m2 surface heat flux) and accounting for compositional heterogeneity in cratonic peridotite xenoliths and the effects of anelasticity. We reviewed various geophysical and petrologic constraints on the nature of cratonic roots (seismic velocities, lithology/mineralogy, electrical conductivity, and gravity) and explored a range of permissible rock and mineral assemblages that can explain the high seismic velocities. These constraints suggest that diamond and eclogite are the most likely high-Vs candidates to explain the observed velocities, but matching the high shear-wave velocities requires either a large proportion of eclogite (>50 vol.%) or the presence of up to 3 vol.% diamond, with the exact values depending on peridotite and eclogite compositions and the geotherm. Both of these estimates are higher than predicted by observations made on natural samples from kimberlites. However, a combination of =20 vol.% eclogite and ~2 vol.% diamond may account for high shear-wave velocities, in proportions consistent with multiple geophysical observables, data from natural samples, and within mass balance constraints for global carbon. Our results further show that cratonic thermal structure need not be significantly cooler than determined from xenolith thermobarometry.
Abstract: Some seismic models derived from tomographic studies indicate elevated shear-wave velocities (=4.7 km/s) around 120-150 km depth in cratonic lithospheric mantle. These velocities are higher than those of cratonic peridotites, even assuming a cold cratonic geotherm (i.e., 35 mW/m2 surface heat flux) and accounting for compositional heterogeneity in cratonic peridotite xenoliths and the effects of anelasticity. We reviewed various geophysical and petrologic constraints on the nature of cratonic roots (seismic velocities, lithology/mineralogy, electrical conductivity, and gravity) and explored a range of permissible rock and mineral assemblages that can explain the high seismic velocities. These constraints suggest that diamond and eclogite are the most likely high-Vs candidates to explain the observed velocities, but matching the high shear-wave velocities requires either a large proportion of eclogite (>50 vol.%) or the presence of up to 3 vol.% diamond, with the exact values depending on peridotite and eclogite compositions and the geotherm. Both of these estimates are higher than predicted by observations made on natural samples from kimberlites. However, a combination of =20 vol.% eclogite and ~2 vol.% diamond may account for high shear-wave velocities, in proportions consistent with multiple geophysical observables, data from natural samples, and within mass balance constraints for global carbon. Our results further show that cratonic thermal structure need not be significantly cooler than determined from xenolith thermobarometry.
Abstract: Some seismic models derived from tomographic studies indicate elevated shear-wave velocities (=4.7 km/s) around 120-150 km depth in cratonic lithospheric mantle. These velocities are higher than those of cratonic peridotites, even assuming a cold cratonic geotherm (i.e., 35 mW/m2 surface heat flux) and accounting for compositional heterogeneity in cratonic peridotite xenoliths and the effects of anelasticity. We reviewed various geophysical and petrologic constraints on the nature of cratonic roots (seismic velocities, lithology/mineralogy, electrical conductivity, and gravity) and explored a range of permissible rock and mineral assemblages that can explain the high seismic velocities. These constraints suggest that diamond and eclogite are the most likely high-Vs candidates to explain the observed velocities, but matching the high shear-wave velocities requires either a large proportion of eclogite (>50 vol.%) or the presence of up to 3 vol.% diamond, with the exact values depending on peridotite and eclogite compositions and the geotherm. Both of these estimates are higher than predicted by observations made on natural samples from kimberlites. However, a combination of =20 vol.% eclogite and ~2 vol.% diamond may account for high shear-wave velocities, in proportions consistent with multiple geophysical observables, data from natural samples, and within mass balance constraints for global carbon. Our results further show that cratonic thermal structure need not be significantly cooler than determined from xenolith thermobarometry.
Journal of Geophysical Research, Vol. 120, 8, pp. 5782-5803.
United States, Arkansas
Geophysics - seismics
Abstract: Global Navigation Satellite System data across the New Madrid seismic zone (NMSZ) in the central United States over the period from 2000 through 2014 are analyzed and modeled with several deformation mechanisms including the following: (1) creep on subsurface dislocations, (2) postseismic frictional afterslip and viscoelastic relaxation from the 1811–1812 and 1450 earthquakes in the NMSZ, and (3) regional strain. In agreement with previous studies, a dislocation creeping at about 4 mm/yr between 12 and 20 km depth along the downdip extension of the Reelfoot fault reproduces the observations well. We find that a dynamic model of postseismic frictional afterslip from the 1450 and February 1812 Reelfoot fault events can explain this creep. Kinematic and dynamic models involving the Cottonwood Grove fault provide minimal predictive power. This is likely due to the smaller size of the December 1811 event on the Cottonwood Grove fault and a distribution of stations better suited to constrain localized strain across the Reelfoot fault. Regional compressive strain across the NMSZ is found to be less than 3?×?10-9/yr. If much of the present-day surface deformation results from afterslip, it is likely that many of the earthquakes we see today in the NMSZ are aftershocks from the 1811–1812 New Madrid earthquakes. Despite this conclusion, our results are consistent with observations and models of intraplate earthquake clustering. Given this and the recent paleoseismic history of the region, we suggest that seismic hazard is likely to remain significant.
Geostandards and Geoanalytical Research, Vol. 43, 2, pp. 291-300.
Global
carbonatites
Abstract: This study presents a high-precision method to measure barium (Ba) isotope compositions of international carbonate reference materials and natural carbonates. Barium was purified using chromatographic columns filled with cation exchange resin (AG50W-X12, 200-400 mesh). Barium isotopes were measured by MC-ICP-MS, using a 135Ba-136Ba double-spike to correct mass-dependent fractionation during purification and instrumental measurement. The precision and accuracy were monitored by measuring Ba isotope compositions of the reference material JCp-1 (coral) and a synthetic solution obtained by mixing NIST SRM 3104a with other matrix elements. The mean d137/134Ba values of JCp-1 and the synthetic solution relative to NIST SRM 3104a were 0.21 ± 0.03‰ (2s, n = 16) and 0.02 ± 0.03‰ (2s, n = 6), respectively. Replicate measurements of NIST SRM 915b, COQ-1, natural coral and stalagmite samples gave average d137/134Ba values of 0.10 ± 0.04‰ (2s, n = 18), 0.08 ± 0.04‰ (2s, n = 20), 0.27 ± 0.04‰ (2s, n = 16) and 0.04 ± 0.03‰ (2s, n = 20), respectively. Barium mass fractions and Ba isotopes of subsamples drilled from one stalagmite profile were also measured. Although Ba mass fractions varied significantly along the profile, Ba isotope signatures were homogeneous, indicating that Ba isotope compositions of stalagmites could be a potential tool (in addition to Ba mass fractions) to constrain the source of Ba in carbonate rocks and minerals.
Crustal structure of the Zimbabwe craton and the Limpopo belt of southern Africa: new constraints from seismic dat a and implications for its evolution.
South African Journal of Geology, Vol. 112, pp. 213-228.
Earth and Planetary Science Letters, Vol. 456, pp. 134-145.
Mantle
Bridgemanite
Abstract: The lower mantle is estimated to be composed of mostly bridgmanite and a smaller percentage of ferropericlase, yet very little information exists for two-phase deformation of these minerals. To better understand the rheology and active deformation mechanisms of these lower mantle minerals, especially dislocation slip and the development of crystallographic preferred orientation (CPO), we deformed mineral analogs neighborite (NaMgF3, iso-structural with bridgmanite) and halite (NaCl, iso-structural with ferropericlase) together in the deformation-DIA at the Advanced Photon Source up to 51% axial shortening. Development of CPO was recorded in situ with X-ray diffraction, and information on microstructural evolution was collected using X-ray microtomography. Results show that when present in as little as 15% volume, the weak phase (NaCl) controls the deformation. Compared to single phase NaMgF3 samples, samples with just 15% volume NaCl show a reduction of CPO in NaMgF3 and weakening of the aggregate. Microtomography shows both NaMgF3 and NaCl form highly interconnected networks of grains. Polycrystal plasticity simulations were carried out to gain insight into slip activity, CPO evolution, and strain and stress partitioning between phases for different synthetic two-phase microstructures. The results suggest that ferropericlase may control deformation in the lower mantle and reduce CPO in bridgmanite, which implies a less viscous lower mantle and helps to explain why the lower mantle is fairly isotropic.
Abstract: We analyzed satellite gravity and geoid anomaly and topography data to determine the 3D lithospheric density structure of the Singhbhum Protocontinent. Our density model shows that distinct vertical density heterogeneities exist throughout the lithosphere beneath the Singhbhum Protocontinent. The crustal structure identified includes a lateral average crustal density variation from 2800 to 2890 kg/m3 as well as a relatively flat Moho at 35-40 km depth in Singhbhum Protocontinent and Bastar Craton. A similar Moho depth range is found for the Mahanadi, Damodar, and Bengal basins. In the northern part of the area, Moho undulates between more than 40 km under the confluence of Mahanadi-Damodar Gondwana basins and the Ganga foreland basin, and 36-32 km under the Eastern Ghats Mobile belt and finally reaches 24 km in the Bay of Bengal. The lithosphere-asthenosphere boundary (LAB) across the Singhbhum Protocontinent is at a depth of about 130-140 km. In the regions of Bastar Craton and Bengal Basin, the LAB dips to about 155 ± 5 km depth. The confluence of Mahanadi and Damodar Gondwana basins toward the north-west and the foreland Ganga Basin toward the north are characterized by a deeper LAB lying at a depth of over 170 and 200 km, respectively. In the Bay of Bengal, the LAB is at a shallower depth of about 100-130 km except over the 85 0E ridge (150 km), and off the Kolkata coast (155 km). Significant density variation as well as an almost flat crust-mantle boundary indicates the effect of significant crustal reworking. The thin (135-140 km) lithosphere provides compelling evidence of lithospheric modification in the Singhbhum Protocontinent. Similarities between the lithospheric structures of the Singhbhum Craton, Chhotanagpur Gneiss Complex, and Northern Singhbhum Mobile Belt confirm that the repeated thermal perturbation controlled continental lithospheric modification in the Singhbhum Protocontinent.
Abstract: Mineral carbonation is a form of carbon capture, utilization and storage (CCUS) that aims to transform excess CO2 into environmentally benign carbonate minerals which are geologically stable. Here, we investigated the reactivity of processed kimberlite and kimberlite ore from the Venetia Diamond Mine (South Africa). Highly reactive phases, such as brucite [Mg(OH)2], are uncommon in the samples collected from Venetia necessitating the development of new strategies for mineral carbonation. Kimberlite ore and tailings from this mine consist of a clay-rich mineral assemblage that is dominated by lizardite (a serpentine mineral) and smectites. Smectites are swelling clays that can act as a source of Mg and Ca for carbonation reactions via cation exchange, dissolution and/or direct replacement of smectites to form carbonate phases. Although carbonation of serpentine and brucite has long been a focus of CCUS in mine wastes [1], smectite carbonation has not been explored in this setting. Quantitative X-ray diffraction using Rietveld refinements coupled with Fourier-transform infrared spectroscopy indicate that smectites of stevensite-saponite composition are abundant in the Venetia samples (1.3-15.4 wt.%). Synchrotron-based X-ray fluorescence mapping correlated with scanning and transmission electron microscopy show that smectites are distributed as altered, smooth regions measuring from 1 to 20 µm in breadth. These phases are rich in Mg and Ca and Al-poor. To better understand the behaviour/reactivity of smectites during the cation exchange process, we have used batch experiments with pure endmembers of Ca-, Mg- and Na-montmorillonite under different treatment conditions (NH4-citrate, NH4-O-acetate, NH4-Cl and Na3-citrate). After 24 hours of reaction, ICP-MS analyses reveal that the four treatments have the same efficiency for Ca and Mg exchange, while NH4-Cl and NH4- O-acetate treatments minimize calcite dissolution. Our end goals are to optimize settling time and to maximize extraction of Ca and Mg for carbonation reactions during ore processing.
Abstract: Using an interdisciplinary approach, this paper reviews current knowledge in the field of natural hydrogen. For the first time, it combines perspectives on hydrogen from the literature of the former Eastern bloc with that of the West, including rare hardcopies and recent studies. Data are summarized and classified in three main sections: hydrogen as a free gas in different environments, as inclusions in various rock types, and as dissolved gas in ground water. This review conclusively demonstrates that molecular hydrogen is much more widespread in nature than was previously thought. Hydrogen has been detected at high concentrations, often as the major gas, in all types of geologic environment. A critical evaluation of all the proposed mechanisms regarding the origin of natural hydrogen shows that a deep-seated origin is potentially the most likely explanation for its abundance in nature. By combining available data, an estimate of 23 Tg/year for the total annual flow of hydrogen from geologic sources is proposed. This value is an order of magnitude greater than previous estimate but most likely still not large enough to account for recently discovered worldwide diffusive seepages. Hydrogen could play a critical role in mechanisms taking place in both the shallow and deep geospheres and it can influence a very wide range of natural phenomena. Hydrogen is an essential energy source for many microorganisms. Sampling for hydrogen can be a useful tool in studying natural environments, geologic mapping, monitoring of earthquakes, plotting fault traces and resource exploration. Hydrogen of geologic origin has the potential to become the renewable energy source of the future, with exploratory projects ongoing at the present time. The topic of natural hydrogen is therefore relevant from many different perspectives.
Contributions to Mineralogy and Petrology, Vol. 171, 7, 14p.
China
Geothermometry
Abstract: The large equilibrium Mg isotope fractionation between clinopyroxene and garnet observed in eclogites makes it a potential high-precision geothermometer, but calibration of this thermometer by natural samples is still limited. Here, we report Mg isotopic compositions of eclogite whole rocks as well as Mg and O isotopic compositions of clinopyroxene and garnet separates from 16 eclogites that formed at different temperatures from the Dabie orogen, China. The whole-rock d26Mg values vary from -1.20 to +0.10 ‰. Among them, 11 samples display limited d26Mg variations from -0.36 to -0.17 ‰, similar to those of their protoliths. The mineral separates exhibit very different d26Mg values, from -0.39 to +0.39 ‰ for clinopyroxenes and from -1.94 to -0.81 ‰ for garnets. The clinopyroxene -garnet Mg isotope fractionation (?26Mgclinopyroxene -garnet = d26Mgclinopyroxene -d26Mggarnet) varies from 1.05 to 2.15 ‰. The clinopyroxene -garnet O isotope fractionation (?18Oclinopyroxene -garnet = d18Oclinopyroxene -d18Ogarnet) varies from -1.01 to +0.98 ‰. Equilibrium Mg isotope fractionation between clinopyroxene and garnet in the investigated samples is selected based on both the d26Mgclinopyroxene versus d26Mggarnet plot and the state of O isotope equilibrium between clinopyroxene and garnet. The equilibrium ?26Mgclinopyroxene -garnet and corresponding temperature data obtained in this study, together with those available so far in literatures for natural eclogites, are used to calibrate the clinopyroxene -garnet Mg isotope thermometer. This yields a function of ?26Mgclinopyroxene -garnet = (0.99 ± 0.06) × 106/T 2, where T is temperature in Kelvin. The refined function not only provides the best empirically calibrated clinopyroxene -garnet Mg isotope thermometer for precise constraints of temperatures of clinopyroxene- and garnet-bearing rocks, but also has potential applications in high-temperature Mg isotope geochemistry.
Contributions to Mineralogy and Petrology, Vol. 175, 18p. Pdf
China
lamproites
Abstract: Lamproites and kimberlites are natural probes of the subcontinental lithospheric mantle providing insights into the Earth’s continental lithosphere. Whole-rock major-, trace-element and Sr-Nd-Pb isotopic compositions of the Paleozoic (~?253 Ma) lamproite dikes from the Baifen zone of the Zhenyuan area in southeastern Guizhou Province (in the southern Yangtze Block, South China) are presented. The Baifen lamproites are characterized by high MgO (7.84-14.1 wt%), K2O (3.94-5.07 wt%) and TiO2 (2.69-3.23 wt%) contents, low SiO2 (41.3-45.7 wt%), Na2O (0.21-0.28 wt%) and Al2O3 (6.10-7.20 wt%) contents. All lamproites have elevated Cr (452-599 ppm) and Ni (485-549 ppm) abundances, as well as high Ba (1884-3589 ppm), La (160-186 ppm), Sr (898-1152 ppm) and Zr (532-632 ppm) concentrations. They show uniform REE distribution patterns that are strongly enriched in light REEs relative to heavy REEs [(La/Yb)N?=?71.1-87.6], and exhibit OIB-like geochemical features with obvious enrichment of both LILEs and HFSEs in the primitive mantle-normalized multi-element distribution diagram. Moderately radiogenic Sr (87Sr/86Sri?=?0.706336-0.707439), unradiogenic Nd (143Nd/144Ndi?=?0.511687-0.511704 and eNd(t)?=??-?12.2 to?-?11.9), and low initial Pb (206Pb/204Pbi?=?16.80-16.90, 207Pb/204Pbi?=?15.34-15.35 and 208Pb/204Pbi?=?37.43-37.70) isotopic compositions are obtained from the rocks. They yield old model ages of TDM(Nd)?=?1.48-1.54 Ga. These signatures suggest that the Baifen lamproite magmas are alkaline, ultrapotassic and ultramafic in character and mainly represent mantle-derived primary melts, which have undergone insignificant crustal contamination and negligible fractional crystallization. The Baifen lamproites originated from a veined metasomatized lithospheric mantle source. We envisage that they were derived by partial melting of old, mineralogically complex metasomatic vein assemblages in the subcontinental lithospheric mantle beneath the southern Yangtze Block. The source region experienced ancient mantle metasomatism with complex modification by enriched fluids and melts. The metasomatic agents are most likely to originate from pre-existing slab subduction beneath the southeastern margin of the Yangtze Block. Tectonically, the Baifen lamproites were emplaced at the southern margin of the Yangtze Block, and they formed in an intraplate extensional setting, showing an anorogenic affinity. In terms of time and space, the genesis of Baifen lamproites is presumably related to the Emeishan large igneous province. The Emeishan mantle plume is suggested as an effective mechanism for rapid extension and thinning of the lithosphere, followed by decompression melting of the subcontinental lithospheric mantle. Combined with the thermal perturbation from asthenospheric upwelling induced by the Emeishan mantle plume, the lamproite magmas, representing small volume and limited partial melts of ancient enriched mantle lithosphere, arose. We propose that the generation of the Baifen lamproite dikes probably was a consequence of the far-field effects of the Emeishan mantle plume.
Delamination and ultra deep subduction of continental crust: constraints from elastic wave velocity and density measurement in ultra high pressure metamorphic rocks
Journal of Metamorphic Geology, Vol. 29, 7, pp. 781-801.
Delamination and ultra deep subduction of continental crust: constraints from elastic wave velocity and density measurement in ultra high pressure metamorphic rocks
Journal of Metamorphic Geology, Vol. 29, 7, pp. 781-801.
Geochemistry, Geophysics, Geosystems, in press available pdf 20p.
Global
geodynamics
Abstract: The relative significance of various geodynamic mechanisms that drive supercontinent breakup is unclear. A previous analysis of extensional stress during supercontinent breakup demonstrated the importance of the plume-push force relative to the dragging force of subduction retreat. Here, we extend the analysis to basal traction (shear stress) and cross-lithosphere integrations of both extensional and shear stresses, aiming to understand more clearly the relevant importance of these mechanisms in supercontinent breakup. More importantly, we evaluate the effect of preexisting orogens (mobile belts) in the lithosphere on supercontinent breakup process. Our analysis suggests that a homogeneous supercontinent has extensional stress of 20-50 MPa in its interior (<40° from the central point). When orogens are introduced, the extensional stress in the continents focuses on the top 80-km of the lithosphere with an average magnitude of ~160 MPa, whereas at the margin of the supercontinent the extensional stress is 5-50 MPa. In both homogeneous and orogeny-embedded cases, the subsupercontinent mantle upwellings act as the controlling factor on the normal stress field in the supercontinent interior. Compared with the extensional stress, shear stress at the bottom of the supercontinent is 1-2 order of magnitude smaller (0-5 MPa). In our two end-member models, the breakup of a supercontinent with orogens can be achieved after the first extensional stress surge, whereas for a hypothetical supercontinent without orogens it starts with more diffused local thinning of the continental lithospheric before the breakup, suggesting that weak orogens play a critical role in the dispersal of supercontinents.
Continental orogenesis from ocean subduction, continent collision/subduction, to orogen collapse, and orogen recycling: the example of the North Qaidam UHPM belt, NW China.
Abstract: Alkaline rock and carbonatite complexes, including the Prairie Lake complex (NW Ontario), are widely distributed in the Canadian region of the Midcontinent Rift in North America. It has been suggested that these complexes were emplaced during the main stage of rifting magmatism and are related to a mantle plume. The Prairie Lake complex is composed of carbonatite, ijolite and potassic nepheline syenite. Two samples of baddeleyite from the carbonatite yield U-Pb ages of 1157.2±2.3 and 1158.2±3.8 Ma, identical to the age of 1163.6±3.6 Ma obtained for baddeleyite from the ijolite. Apatite from the carbonatite yields the same U-Pb age of ~1160 Ma using TIMS, SIMS and laser ablation techniques. These ages indicate that the various rocks within the complex were synchronously emplaced at about 1160 Ma. The carbonatite, ijolite and syenite have identical Sr, Nd and Hf isotopic compositions with a 87Sr/86Sr ratio of ~0.70254, and positive eNd
