Hello Guest User, You are visiting this website from a computer with an IP address of 172.71.254.26 with the name of '?' since Fri Apr 19, 2024 at 10:28:37 AM PT for approx. 0 minutes now.
SDLRC - Scientific Articles all years by Author - X
The Sheahan Diamond Literature Reference Compilation
The Sheahan Diamond Literature Reference Compilation is compiled by Patricia Sheahan who publishes on a monthly basis a list of new scientific articles related to diamonds as well as media coverage and corporate announcementscalled the Sheahan Diamond Literature Service that is distributed as a free pdf to a list of followers. Pat has kindly agreed to allow her work to be made available as an online digital resource at Kaiser Research Online so that a broader community interested in diamonds and related geology can benefit. The references are for personal use information purposes only; when available a link is provided to an online location where the full article can be accessed or purchased directly. Reproduction of this compilation in part or in whole without permission from the Sheahan Diamond Literature Service is strictly prohibited. Return to Diamond Resource Center
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
The SDLRC provides 3 types of references identified in the reference code. DS for scientific article, DM for a media article, and DC for a corporate announcement. Consider DS0512-0001. The DS stands for "diamond scientific". 05 stands for 2005, the year the reference was posted. 12 represents the month the reference was posted. For all years prior to 2015 the default month is 12. -0001 is the reference's identifier and it does not mean anything. The number below the refence code, ie 2015, is the year the article was published. Note that the posted year may sometimes be later than the published year.
Sort Order
References are sorted by the "author" name and when the reference was posted to the compilation.
Most Recent
If the reference code is highlighted yellow, the reference was made available through the most recent monthly compilation of new literature. Use this to check out new references. When new references are posted, we make it our priority to track down an online link and obtain an abstract. With regard to older references, tracking down an abstract and an online link is a work in progress.
Link to external location of article:
If the title has a link, it means we have found a location online where you can either retrieve the full article free, or purchase access to it. The Sheahan Diamond Literature Service is not a technical article procurement service; if you want a restricted article, you must deal directly with the vendor who controls the copyright to the article.
Searching this page for a specific term or author
In your Firefox browser click Edit in the menu bar and then Find. In the Find box that shows up at the bottom of the web page enter your search term. Firefox will highlight all occurrences. This is particularly helpful when the author you are seeking was not the lead author by whom the compilation is sorted.
Sending or sharing a reference
The left column (Posted/Published) has an embedded hyperlink for each reference. In Firefox, if you right click on it, you can obtain the link url for that reference's location within the page, which you can copy and paste into an email or any other document. You can also use the "share this link" option to tweet, facebook etc the link.
Earth and Planetary Science Letters, Vol. 490, 1, pp. 161-169.
Mantle
geothermometry
Abstract: In this study, we have determined the phase boundary between Mg0.735Fe0.21Al0.07Si0.965O3-Bm and PPv and the thermal equations of state of both phases up to 202 GPa and 2600 K using synchrotron X-ray diffraction in laser heated diamond anvil cells. Our experimental results have shown that the combined effect of Fe and Al produces a wide two-phase coexistence region with a thickness of 26 GPa (410 km) at 2200 K, and addition of Fe lowers the onset transition pressure to 98 GPa at 2000 K, consistent with previous experimental results. Furthermore, addition of Fe was noted to reduce the density (?) and bulk sound velocity () contrasts across the Bm-PPv phase transition, which is in contrast to the effect of Al. Using the obtained phase diagram and thermal equations of state of Bm and PPv, we have also examined the effect of composition variations on the ? and
profiles of the lowermost mantle. Our modeling results have shown that the pyrolitic lowermost mantle should be highly heterogeneous in composition and temperature laterally to match the observed variations in the depth and seismic signatures of the D? discontinuity. Normal mantle in a pyrolitic composition with ?10% Fe and Al in Bm and PPv will lack clear seismic signature of the D? discontinuity because the broad phase boundary could smooth the velocity contrast between Bm and PPv. On the other hand, Fe-enriched regions close to the cold slabs may show a seismic signature with a change in the velocity slope of the D? discontinuity, consistent with recent seismic observations beneath the eastern Alaska. Only regions depleted in Fe and Al near the cold slabs would show a sharp change in velocity. Fe in such regions could be removed to the outer core by strong core-mantle interactions or partitions together with Al to the high-pressure phases in the subduction mid ocean ridge basalts. Our results thus have profound implication for the composition of the lowermost mantle.
Abstract: Geophysical investigations and laboratory experiments provide strong evidence for subduction of ancient oceanic crust, and geological and mineralogical observations suggest that subducted oceanic crust is recycled into the upper mantle. This model is supported by some direct petrologic and miner-alogical evidence, principally the recovery of super-deep diamonds from kimberlites and the presence of crustal materials in ophiolitic chromitites and peridotites, but many details are still unclear. Here we report the discovery of ophiolite-hosted diamonds in the podiform chromitites of the Skenderbeu massif of the Mirdita ophiolite in the western part of Neo-Tethys. The diamonds are characterized by exceedingly light C isotopes (?13CPDB ~ -25), which we interpret as evidence for subduction of organic carbon from Earth's surface. They are also characterized by an exceptionally large range in ? 15Nair (-12.9 to +25.5), accompanied by a low N aggregation state. Materials sparsely included in diamonds include amorphous material, Ni-Mn-Co alloy, nanocrystals (20 Χ 20 nm) of calcium silicate with an orthorhombic perovskite structure (Ca-Pv), and fluids. The fluids coexisting with the alloy and Ca-Pv provide clear evidence that the diamonds are natural rather than synthetic. We suggest that the Skenderbeu diamonds nucleated and grew from a C-saturated, NiMnCo-rich melt derived from a subducted slab of ocean crust and lithosphere in the deep mantle, at least in the diamond stability field, perhaps near the top of the mantle transition zone. The subsequent rapid upward transport in channeled networks related to slab rollback during subduction initiation may explain the formation and preservation of Skenderbeu diamonds. The discovery of diamonds from the Mirdita ophiolite not only provides new evidence of diamonds in these settings but also provides a valuable opportunity to understand deep cycling of subducted oceanic crust and mantle composition.
Earth Science Reviews, in press available, 38p. Doi.org/1010.1016 /jearsciev.2019.103073
Global
carbon
Abstract: Although the deep recycling of carbon has been proposed to play a key role in producing intraplate magmatism, the question of how it controls or triggers mantle melting remains poorly understood. In addition, generation of incipient carbonated melts in the mantle and their subsequent reaction with the mantle are critical processes that can influence the geochemistry of intraplate basalts, but the details of such processes are also unclear. Here we present geochemical evidence for the existence of pervasive carbonate melt in the mantle source of Cenozoic continental intraplate highly alkali basalts (SiO2 < 45 wt%), which are volumetrically minor but widespread in eastern China. The primary magma compositions of these basalts cannot be explained by either partial melting of a single mantle source lithology or mixing of magmas derived from distinct mantle sources, but can be adequately explained by carbonate-fluxed melting of eclogite and subsequent reaction between silica-rich melts and peridotite that ultimately transformed the initial carbonated silica-rich melts into silica-undersaturated alkalic magmas. The source of the carbonate is in subducted eclogites associated with the Pacific plate, which stagnated in the mantle transition zone (MTZ). The spatial distribution of the alkali basalts is in accord with large-scale seismic low-velocity anomalies in the upper mantle above the MTZ. Similar scenarios in central-western Europe and eastern Australia lead us to propose that reaction between carbonated silica-rich melt and peridotite may be a pivotal mechanism for the generation of continental intraplate alkali basalts elsewhere in the world.
Abstract: Carbonates are common rock-forming minerals in the Earths crust and act as sinks of atmospheric carbon dioxide. Subduction of hydrothermally altered oceanic lithosphere returns carbon to the interior, where more than three quarters of Earths carbon is stored. The contribution of subducted carbonates to the Earth's long-term deep carbon cycle is uncertain and has recently emerged as a topic of intense debate [1]. Moreover, mantle-slab interaction has been proposed as a mechanism to produce super-deep diamonds, thus questioning the use of certain mineral inclusions to infer lower-mantle origin [2]. Here we report new data on the chemical stability and reaction kinetics of carbonates in the mantle from multianvil and diamond-anvil-cell experiments. Our results suggest that carbon can be sequestered into deep Earth through reaction freezing and that the index minerals for super-deep diamonds are not reliable indicators for their formation depths.
Geochemical Perspectives Letters, Vol. 11, pp. 18-22.
Mantle
nitrogen
Abstract: Nitrogen and carbon are essential elements for life, and their relative abundances in planetary bodies are important for understanding planetary evolution and habitability. The high C/N ratio in the bulk silicate Earth (BSE) relative to chondrites has been difficult to explain through partitioning during core formation and outgassing from molten silicate. Here we propose a new model that may have released nitrogen from the metallic cores of accreting bodies during impacts with the early Earth. Experimental observations of melting in the Fe-N-C system via synchrotron X-ray radiography of samples in a Paris-Edinburgh press reveal that above the liquidus, iron-rich melt and nitrogen-rich liquid coexist at pressures up to at least 6 GPa. The combined effects of N-rich supercritical fluid lost to Earths atmosphere and/or space as well as N-depleted alloy equilibrating with the magma ocean on its way to the core would increase the BSE C/N ratio to match current estimates.
Mineralium Deposita, 10.1007/s00126 -021-01055-2 18p. Pdf
China
carbonatites
Abstract: The Huangshui'an deposit located in East Qinling (China) is an unusual case of a Si-rich carbonatite hosting economic Mo and minor Pb and REE mineralization. The role of mantle-sourced carbonatite melts and fluids in the formation of the Mo mineralization remains poorly understood. Our integrated study based on field geology, petrography, microthermometry, and LA-ICP-MS analysis of single fluid inclusions, and noble gas isotopes of pyrite permits to reconstruct the source characteristics, the magmatic-hydrothermal evolution of the carbonatitic fluids, and their controls on Mo mineralization. Fluid inclusions hosted in calcite in the carbonatite dikes have the highest concentrations of Mo (9.9-62 ppm), Ce (820-9700 ppm), Pb (1800-19500 ppm), and Zn (570-5800 ppm) and represent the least modified hydrothermal fluid derived from the carbonatite melt. Fluid inclusions hosted in calcite (Cal) and quartz (Qz2 and Qz3) of the stage I carbonatite dikes have different metal concentrations, suggesting that they formed from two distinct end member fluids. The FIA in calcite represent fluid A evolved from carbonatite melt with relatively high-ore metal concentrations, and those in quartz characterize fluid B having a crustal signature due to metasomatic reactions with the wall rocks. The FIA in quartz (Qz1) within the altered wall rock have overlapping elemental concentrations with those of massive quartz (Qz2) and vuggy quartz (Qz3) in carbonatite. This suggests that the volumetrically significant quartz in the Huangshui'an carbonatite has been formed by the introduction of Si by fluid B. The positive correlations between Rb, B, Al, Cl, and Sr in stage II fluid inclusions in late fluorite + quartz + calcite veins indicate that this late mineralization formed from the mixing of primary hydrothermal fluid B with meteoric water. The He-Ar isotope data, in combination with available C-O-Sr-Nd-Pb isotope data, constrain the carbonatite source as an enriched mantle source modified by contributions from crustal material which was probably the fertile lower crust in the region. This distinct source facilitated the enrichment in Mo, REE, and Pb in the primary carbonatite magma. The carbonatite magmatism and Mo mineralization at 209.5-207 Ma occurred in the regional-scale extensional setting at the postcollision stage of the Qinling Orogenic Belt.
Abstract: The unique, giant, rare earth element (REE) deposit at Bayan Obo, northern China, is the worlds largest REE deposit. It is geologically complex, and its genesis is still debated. Here, we report in situ Th-Pb dating and Nd isotope ratios for monazite and Sr isotope ratios for dolomite and apatite from fresh drill cores. The measured monazite ages (361-913 Ma) and previously reported whole-rock Sm-Nd data show a linear relationship with the initial Nd isotope ratio, suggesting a single-stage evolution from a Sm-Nd source that was formed before 913 Ma. All monazites show consistent ?Nd(1.3Ga) values (0.3 ± 0.6) close to those of the adjacent 1.3 Ga carbonatite and mafic dikes. The primary dolomite and apatite show lower 87Sr/86Sr ratios (0.7024-0.7030) than the recrystallized dolomite (0.7038-0.7097). The REE ores at Bayan Obo are interpreted to have originally formed as products of ca. 1.3 Ga carbonatitic magmatism and to have undergone subsequent thermal perturbations induced by Sr-rich, but REE-poor, metamorphic fluids derived from nearby sedimentary rocks.
Wang, Q., Ji, S., Salisbury, M.H., Xia, B., Pan, M., Xu, Z.
Pressure dependence and anisotropy of P wave velocities in ultrahigh pressure metamorphic rocks from the Dabie Sulu orogenic belt: implications for seismic properties
Wang, Q., Shaocheng, J., Salisbury, M.H., Xia, B., Pan, M., Xu, Z.
Shear wave properties and Poisson's ratios of ultrahigh pressure metamorphic rocks from the Dabie Sulu orogenic belt, China: implications for crustal composition.
Journal of Geophysical Research, Vol. 110, B8, pp. B08411 10.1029/2004 JB003435
Abstract: The continental lithosphere is not forever; some cratons have lost their original roots during the course of their evolution. Yet, it is not clear whether gravitational instability of dense lower crust is the primary driver of decratonization. This is addressed here with emphasis being placed on the North China Craton (NCC), because it represents one of the best examples of craton-root disruption in the world, and a place where models can be tested. If lower-crustal delamination was the trigger for decratonization, we would expect a clear contrast in crustal structure and composition between disturbed (rootless) and intact cratons. However, the eastern (disturbed) and western (intact) parts of the NCC show virtually identical physical structure and composition (a thin mafic lower crust and a predominantly intermediate composition overall) although the crust in the disturbed part is thinner than in the intact craton. This suggests that delamination of the lower crust was not a viable mechanism of craton-root disruption in the NCC case. Indeed, the crust beneath the NCC largely resembles those of stable Archean cratons worldwide. Therefore the delamination, if it occurred, may have taken place much earlier (Archean) than previously thought, rather than in the Mesozoic. Delamination may have been a common phenomenon in the early evolution of cratons, probably due to relatively higher mantle temperatures in the Archean Eon.
Diamonds & Related Materials, in press available, 31p. Pdf
Global
carbon
Abstract: Natural diamonds that have been partially replaced by graphite have been observed to occur in natural rocks. While the graphite-to-diamond phase transition has been extensively studied the opposite of this (diamond to graphite) remains poorly understood. We performed high-pressure and temperature hydrous and anhydrous experiments up to 1.0?GPa and 1300?°C using Amplex premium virgin synthetic diamonds (20-40??m size) as the starting material mixed with Mg (OH)2 as a source of H2O for the hydrous experiments. The experiments revealed that the diamond-to-graphite transformation at P?=?1GPa and T?=?1300?°C was triggered by the presence of H2O and was accomplished through a three-stage process. Stage 1: diamond reacts with a supercritical H2O producing an intermediate 200-500?nm size globular carbon phase. This phase is a linear carbon chain; i.e. a polyyne or carbyne. Stage 2: the linear carbon chains are unstable and highly reactive, and they decompose by zigzagging and cross-linking to form sp2-bonded structures. Stage 3: normal, disordered, and onion-like graphite is produced by the decomposition of the sp-hybridized carbon chains which are re-organized into sp2 bonds. Our experiments show that there is no direct transformation from sp3 C-bonds into sp2 C-bonds. Our hydrous high-pressure and high-temperature experiments show that the diamond-to-graphite transformation requires an intermediate metastable phase of a linear hydrocarbon. This process provides a simple mechanism for the substitution of other elements into the graphite structure (e.g. H, S, O).
Earth and Planetary Science Letters, Vol. 464, pp. 103-115.
Mantle
Geochronology
Abstract: To better constrain the Cr isotopic composition of the silicate Earth and to investigate potential Cr isotopic fractionation during high temperature geological processes, we analyzed the Cr isotopic composition of different types of mantle xenoliths from diverse geologic settings: fertile to refractory off-craton spinel and garnet peridotites, pyroxenite veins, metasomatised spinel lherzolites and associated basalts from central Mongolia, spinel lherzolites and harzburgites from North China, as well as cratonic spinel and garnet peridotites from Siberia and southern Africa. The ?53CrNIST 979 values of the peridotites range from ?0.51±0.04?0.51±0.04 (2SD) to +0.75±0.05+0.75±0.05 (2SD). The results show a slight negative correlation between ?53Cr and Al2O3 and CaO contents for most mantle peridotites, which may imply Cr isotopic fractionation during partial melting of mantle peridotites. However, highly variable Cr isotopic compositions measured in Mongolian peridotites cannot be caused by partial melting alone. Instead, the wide range in Cr isotopic composition of these samples most likely reflects kinetic fractionation during melt percolation. Chemical diffusion during melt percolation resulted in light Cr isotopes preferably entering into the melt. Two spinel websterite veins from Mongolia have extremely light ?53Cr values of ?1.36±0.04?1.36±0.04 and ?0.77±0.06?0.77±0.06, respectively, which are the most negative Cr isotopic compositions yet reported for mantle-derived rocks. These two websterite veins may represent crystallization products from the isotopically light melt that may also metasomatize some peridotites in the area. The ?53Cr values of highly altered garnet peridotites from southern Africa vary from ?0.35±0.04?0.35±0.04 (2SD) to +0.12±0.04+0.12±0.04 (2SD) and increase with increasing LOI (Loss on Ignition), reflecting a shift of ?53Cr to more positive values by secondary alteration.
Abstract: Mantle metasomatism by percolating melts/fluids can significantly modify the geochemical and mineralogical compositions of the sub-continental lithospheric mantle (SCLM). We present a detailed study of water contents and Li concentrations and isotopic compositions in mantle minerals from a suite of peridotite xenoliths entrained by a Cenozoic Strombolian volcano in the southern French Massif Central (FMC). Wide ranging clinopyroxene trace element distributions (e.g., (La/Yb)N from 0.25 to 22.21; Ti/Eu ratios from 453 to 4892) suggest that the SCLM has undergone metasomatism by carbonatitic melts/fluids or melts/fluids related to subducted materials. Two amphibole-bearing samples exhibit depletion of light rare earth elements (LREE; (La/Yb)N = 0.26 and 0.30, respectively) in amphiboles, similar to that in co-existing clinopyroxenes; these samples indicate that amphiboles grew during a separate modally metasomatic event predating the cryptic metasomatism accounting for LREE enrichment and negative HFSE anomalies in other samples. Mineral Li concentrations are similar to those in the normal mantle, with inter-mineral Li partitioning nearly equilibrated and intragranular Li distributions nearly homogeneous. However, negative ?7Li values of pyroxenes in some samples (as low as ? 8.8 in clinopyroxene of sample MC38) can be attributed to diffusive exchange with a small-volume melt of moderate Li concentration and light Li isotopic composition, originally associated with a recycled component. Preservation of the currently observed large inter-mineral Li isotopic variations indicates that melt percolation occurred shortly before entrainment of the peridotite xenoliths by the host magma. Mineral water contents vary from 41 to 428 ppm in clinopyroxenes and from 28 to 152 ppm in orthopyroxenes, and their roughly negative co-variation with coexisting olivine Fo contents imply that partial melting was the main control over mineral water content variations in most samples. Varied water contents in LREE-enriched metasomatized samples indicate the involvement of metasomatic agents of different origins. The aqueous agent responsible for generation of amphiboles in two samples did not produce a notable increase in the water contents of coexisting nominally anhydrous minerals.
Abstract: Both mantle-derived clinopyroxene and orthopyroxene are generally homogeneous in water concentration, while water content in the coexisting olivine is affected by partial or complete loss during the ascent of the hosting magma. Here, we report the first record of water content profiles (higher water in the cores than in the rims) in natural orthopyroxene grains in peridotite xenoliths hosted by Cenozoic alkali basalts in Tianchang volcano, eastern China. The water contents of the coexisting clinopyroxene grains are homogeneous and are twice that measured in the cores of orthopyroxene grains, confirming previous chemical equilibrium between the two pyroxenes. The olivines (ol) are nearly dry (?0 ppm). These observations demonstrate that H diffusion in mantle orthopyroxene (opx) is faster than in clinopyroxene (cpx), and the relative mobility of H in each mineral phase could be quantified as: Graphic (where is the chemical diffusion coefficient of hydrogen). Combining this with experimental diffusion coefficients from the literature, we infer that (1) the xenoliths remained in contact with the magma below 900 °C for several months, and (2) clinopyroxene remains the more reliable recorder of water from depth, and orthopyroxene should be used more cautiously but can be considered with olivine for tracing slow transport and cooling of magma.
Multistage growth of garnet in ultrahigh pressure eclogite during continental collision in the Dabie Orogen: constrained by trace elements and U Pb ages.
Abstract: To investigate lateral and depth variations of seismic anisotropy beneath the central-western United States, we determined a detailed 3-D model of P-wave anisotropic tomography by inverting a large number of arrival-time data of local and teleseismic events. Our results reveal significant azimuthal anisotropies in the crust and lithosphere, which are associated with ancient orogenic collisional and magmatic activities. As depth increases, the fast-velocity direction (FVD) pattern becomes gradually trended and small features fade away. There is a boundary in the FVD distribution, which separates the tectonically active region in the west from the stable cratonic region in the east. Frozen-in anisotropy with a NW-SE FVD is preserved in the thick Wyoming cratonic lithosphere that exhibits as a high-velocity (high-V) anomaly to a depth of ~250 km. In the asthenosphere beneath the western thin lithosphere, FVDs are generally parallel with the absolute motion direction of the North American plate due to shearing between the plate and the asthenosphere. In the deeper areas, the subducted and fragmented slab exhibiting as high-V anomalies leads to slab-related mantle flows. These results indicate that seismic anisotropies exist in both the lithosphere and asthenosphere with different geodynamic mechanisms and it is feasible to link the P-wave azimuthal anisotropy to lithospheric deformations, fossil anisotropy in the lithosphere, and flows in the asthenosphere.
Geophysical Research Letters, Vol. 46, 2, pp. 678-688.
Global
craton
Abstract: Low??18O magma has received great attention and it has profound implications on geological and climate evolution. Neoproterozoic era is a unique period to breed low??18O magmas and snowball Earth. This manuscript first report Neoproterozoic moderately 18O?depleted zircons from the central part of the Cathaysia Block in South China, and it builds a four end?member Hf?O isotopic mixing model to explain the global low??18O magmas at Neoproterozoic era. Our compilation of low??18O zircon data and our new data confirms that globally Neoproterozoic 18O?depleted magmatic activities generally began after 800 Ma and reached a peak at 780-760 Ma. This provides new information on the rifting of Rodinia supercontinent and suggests close connections between northwest India, Madagascar, and South China in the Rodinia supercontinent. This manuscript deals with the hot?debated topics on oxygen isotopes and supercontinent cycle. We believe that this manuscript will attract international readers from a wide scope of geosciences.
Geophysical Research Letters, Vol. 46, 4, pp. 2012-2024.
South America, Colombia, Australia
craton
Abstract: Significant amounts of landmasses are brought together in a hemispheric supercontinent, then breaks up, disperse, and reform in a new supercontinent in every 400-450 Myrs. During the supercontinent cycle, global?scale continental magmatism and orogenic activity increased. The assembly and breakup of Pangaea, the latest supercontinent, are well understood today. However, the evidence becomes more sparse further back in geological history. The geological and paleomagnetic data are insufficient to determine the exact geometries of Rodinia and Columbia supercontinents. Hence, we trace the position of Cathaysia block in the Columbia supercontinent and its relationship with other continental blocks, based on its Paleoproterozoic magmatisms, metamorphisms, and sedimentations, especially ultradepleted mantle?derived rocks. This work has important implications for the mantle heterogeneity in supercontinent reconstruction.
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 Earths 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 ?Nd(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.
Abstract: Crustal zircon xenocrysts from mantle-derived magmatic rocks have the potential to probe the deep crust. Here we present integrated U-Pb dating and Hf-isotope analyses of zircons from a Paleozoic diamondiferous kimberlite dike in the Maping area of Zhenyuan County (southeastern Guizhou Province), with implications for the tectonothermal evolution of unexposed continental crust beneath the southern Yangtze Block, South China. All zircons (n = 236) show a wide range of U-Pb ages between Mesoarchean and middle Carboniferous. Among them, 96 zircons with 90-110% concordance yield concordant ages from 2942 ± 8 Ma to 342 ± 2 Ma, and form major age peaks at ?2.9 Ga, ?2.6 Ga and ?2.0 Ga. The overwhelming majority of zircons are dominated by Mesoarchean-Paleoproterozoic U-Pb ages regardless of their concordance degrees. The zircon populations mainly consist of magmatic zircons, with minor metamorphic grains (Th/U < 0.10). The youngest magmatic zircon (Th/U = 0.43) with a well concordant 206Pb/238U age of 342 ± 2 Ma (M1-16) is interpreted as the maximum emplacement age of the Maping diamondiferous kimberlites. Most zircons with pre-eruption ages are considered to be xenocrysts, and they may be derived from the deep-seated continental crust through which kimberlite host magmas have passed. Their U-Pb ages and Hf isotopic compositions suggest the possible existence of a highly evolved Archean basement beneath the southern Yangtze Block, South China, which is much older than its known surface rocks. A lot of magmatic zircon xenocrysts reveal complex Precambrian crustal evolution in the southern Yangtze Block. These processes involved the important growth of continental crust at 2.6-2.5 Ga, and in the meantime, crustal reworking could be intermittently proceeding at 3.0-2.6 Ga. In addition, a group of xenocrystic zircons are identified to be of metamorphic origin, indicating that the proposed Archean basement beneath the southern Yangtze Block likely experienced a metamorphic event around 2.0 Ga. This geologically significant episode is consistent with the well-developed coeval metamorphism in other places of the Yangtze Block (e.g., Kongling Terrane), which has been considered to link to the assembly of the Paleoproterozoic Nuna/Columbia supercontinent. Our zircon data implies that the unexposed Archean basement beneath the southern Yangtze Block was affected by multiple thermal activities.
Abstract: Magnesium and oxygen are critical elements in the solid Earth and hydrosphere. A better understanding of the combined behavior of Mg and O isotopes will refine their use as a tracer of geochemical processes and Earth evolution. In this study, the Mg-isotope compositions of garnet and omphacite separated from well-characterized xenolithic eclogites from the Roberts Victor kimberlite pipe (South Africa) have been measured by solution multi-collector ICP-MS. The reconstructed whole-rock ?26Mg values of Type I (metasomatized) eclogites range from ? 0.61 to ? 0.20 (Type IA) and from ? 0.60 to ? 0.30 (Type IB) (mean ? 0.43 ± 0.12), while ?26Mg of Type IIA (fresh, least metasomatized) eclogites ranges from ? 1.09 to ? 0.17 (mean ? 0.69 ± 0.41); a Type IIB (fresh, least metasomatized) has ?26Mg of ? 0.37. Oxygen-isotope compositions of garnet were analyzed in situ by SIMS (CAMECA 1280) and cross-checked by laser fluorination. Garnets have ?18O of 6.53 to 9.08 in Type IA, 6.14 to 6.65 in Type IB, and 2.34 to 2.91 in Type IIB. The variation of ?26Mg and ?18O in Type IA and IB eclogites is consistent with the previously proposed model for the evolution of these samples, based on major and trace elements and radiogenic isotopes. In this model, the protoliths (Type II eclogites) were metasomatized by carbonatitic to kimberlitic melts/fluids to produce first Type IA eclogites and then Type IB. Metasomatism has changed the O-isotope compositions, but the Mg-isotope compositions of Type IA are mainly controlled by the protoliths; those of Type IB eclogites reflect mixing between the protoliths and the kimberlitic melt/fluid. The combination of a large range of ?26Mg and low ?18O in Type II eclogites cannot be explained easily by seawater alteration of oceanic crust, interaction of carbonate/silicate sediments with oceanic crust, or partial melting of mafic rocks.
The Canadian Mineralogist, Vol. 54, pp. 1285-1291.
China, Mongolia
carbonatite - Bayan Obo
Abstract: Fluorcalciopyrochlore, ideally (Ca,Na)2Nb2O6F, cubic, is a new mineral species (IMA2013-055) occurring in the Bayan Obo Fe-Nb-REE deposit, Inner Mongolia, People's Republic of China. The mineral is found in a dolomite-type niobium rare-earth ore deposit. Associated minerals are dolomite, aegirine, riebeckite, diopside, fluorite, baryte, phlogopite, britholite-(Ce), bastnδsite-(Ce), zircon, magnetite, pyrite, fersmite, columbite-(Fe), monazite-(Ce), rutile, and others. Crystals mostly form as octahedra {111}, dodecahedra {110}, and cubes {100}, or combinations thereof, and generally range in size from 0.01 to 0.3 mm. It is brownish-yellow to reddish-orange in color with a light yellow streak. Crystals of fluorcalciopyrochlore are translucent to transparent with an adamantine to greasy luster on fractured surfaces. It has a conchoidal fracture. No parting or cleavage was observed. The Mohs hardness is 5, and the calculated density is 4.34(1) g/cm3. The empirical formula is (Ca1.14Na0.74Ce0.06Sr0.03Th0.01Fe0.01Y0.01La0.01Nd0.01)?2.02(Nb1.68Ti0.29Zr0.02Sn0.01)?2.00O6.00(F0.92O0.08)?1.00 on the basis of 7(O,F) anions pfu. The simplified formula is (Ca,Na)2Nb2O6F. The strongest four reflections in the X-ray powder-diffraction pattern [d in Ε (I) hkl] are: 6.040 (9) 1 1 1, 3.017 (100) 2 2 2, 2.613 (17) 0 0 4, 1.843 (29) 0 4 4, and 1.571 (15) 2 2 6. The unit-cell parameters are a 10.4164(9) Ε, V 1130.2(2) Ε3, Z = 8. The structure was solved and refined in space group FdEmbedded Image m with R = 0.05. The type material is deposited in the Geological Museum of China, Beijing, People's Republic of China, catalogue number M12182.
Geochronology and geochemistry of felsic xenoliths in lamprophyre dikes from the southeastern margin of the North Chin a Craton: implications for the interleaving of the Dabie Sulu orogenic crust.
International Geology Review, Vol. 57, 9-10, pp. 1305-1325.
Diamond & Related Materials, Vol. 88, pp. 110-117.
Mantle
diamond morphology
Abstract: Dislocation nucleation plays a key role in plastic deformation of diamond crystal. In this paper, homogeneous and heterogeneous nucleation nature for diamond glide set dislocation and shuffle set dislocation is studied by combining molecular dynamics method and continuum mechanics models. Our results show that although heterogeneous dislocation nucleation can decrease its activation energy, the activation energy at 0?GPa for diamond heterogeneous nucleation is still in the range of 100?eV. For glide set and shuffle set homogeneous nucleation, their critical nucleation shear stress approaches to diamond's ideal shear strength which implies that those dislocations do not nucleate before diamond structural instability only by a purely shearing manner. While for glide set and shuffle set heterogeneous nucleation, their critical nucleation shear stresses are 28.9?GPa and 48.2?GPa, these values are less than diamond's ideal shear strength which implies that these dislocations may be nucleated heterogeneously under certain shear stress condition. In addition, our results also indicate there exists a deformation mode transformation for diamond deformation behavior at strain rate of 10?3/s. Our results provide a new insight into diamond dislocation nucleation and deformation.
Distinct mantle sources of low Ti and high Ti basalts from the western Emeishan large igneous province, SW China: implications for plume?? lithosphere interaction
Earth and Planetary Science Letters, Vol. 228, 3-4, pp. 525-546.
Diamond and Related Materials, in press available, 29p.
Technology
Synthetics - nitrogen
Abstract: This study describes the growth of 13C-enriched (100)-oriented diamond single crystals by the MPCVD (microwave plasma chemical vapour deposition) process. All crystals are at least 6 Χ 6 mm2 in area and 0.5-1.0 mm in thickness. The samples with nominal 13C percentages (R = [13C] / [13C + 12C]) of 0.011 (natural abundance), 0.10, 0.21, 0.24 and 0.34 were obtained by controlling the flow of the carbon-13 and carbon-12 methane feed gases. To obtain thicker and near-colourless quality 13C-enriched diamond, 190 ppm of nitrogen was added into the gas mixture. The shift towards lower frequency in the Raman peak positions and decrease in the thermal conductivities of the near-colourless crystals with increasing 13C percentages are similar to previous studies of isotopically-controlled diamond grown with no nitrogen additive. The images of the structural defects associated with 13C-enrichment obtained by spatially-resolved X-ray rocking curve measurement show distinct patterned structures that runs parallel to the < 100 > direction. Moreover, the broadening in the line width of the nuclear magnetic resonance (NMR) peak from sp313C correlates with increasing R. We also expand the study by injecting 500 ppm of nitrogen. Higher nitrogen concentration leads to the formation of brown crystals. The brown crystals show far greater 13C NMR peak intensity than the near-colourless. This suggests that paramagnetic nitrogen impurities in the brown crystals hasten the spin-lattice relaxation time of the 13C nuclear spin that resulted in higher intensity. The isotopic splitting observed for the localized vibrational mode of the NVH0 defect in brown crystals is attributed to the co-existence of both the 13C (3114.2 cm? 1) and 12C (3123.5 cm? 1). Unlike the isotopic splitting observed for NVH0 defect, the peak position of the Ns+ defect shifts towards lower frequency as R increases. Not only have we demonstrate the growth of bigger isotopically-controlled diamond single crystals, the results shown here have provided a framework to further investigate the interplay between 13C atoms and nitrogen impurity.
Abstract: We have found >10 in situ microdiamonds in thin sections of eclogites from the Dabie and Su-Lu regions of central eastern China since the first occurrence of microdiamond in eclogites from the Dabie Mountains (DMT) reported in 1992. The microdiamonds are found not only in the central part but also in the northern part of the DMT. Several free crystals have been recovered from the crushed eclogites from the central DMT. Most in situ microdiamonds are inclusions in garnets but a few larger ones are intergranular. Most of the diamondiferous eclogites in the central part of the DMT are associated with coesite. Most importantly, the observation of microdiamonds in northern Dabie lead us to question the supposition that this is a low-P metamorphic terrane. All the diamondiferous eclogites from both the north and central DMT are of continental affinity as demonstrated by their negative ?Nd values. Therefore, both the north and central eclogite belts in the DMT are considered to be from the deep subducted terrane. Five in situ microdiamonds and two free crystals are first reported in this paper. The dimensions of the in situ microdiamonds are 30-80 ?m and the free crystals are up to 400-00 ?m across. All the microdiamonds are confirmed as such by Raman spectroscopy. The results of an infrared spectroscopic investigation on two larger free crystals and two in situ microdiamonds show that all the microdiamonds from both the Dabie and Su-Lu regions are mixed types IaA and IaB diamonds and there is no indication of any synthetic microdiamonds in our samples because such synthetic microdiamonds are always rich in type Ib.
Su, B-X., Zhang, H-F., Ying, J-F., Xiao, Y., Zhao, X-M.
Nature and processes of the lithospheric mantle beneath the western Qinling: evidence from deformed peridotitic xenoliths in Cenozoic kamafugite from Haoiti, Gansu Pro
Journal of Asian Earth Sciences, Vol. 34, 3, pp. 258-274.
Su, B-X., Zhang, H-F., Ying, J-F., Xiao, Y., Zhao, X-M.
Nature and processes of the lithospheric mantle beneath the western Qinling: evidence from deformed peridotitic xenoliths in Cenozoic kamafugite from Haoti Province.
Journal of Asian Earth Sciences, Vol. 34, pp. 258-274.
Highly heterogeneous lithospheric mantle beneath the Central Zone of the North Chin a Craton evolved from Archean mantle through diverse melt refertilization.
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 ?26Mg values vary from ?1.20 to +0.10 . Among them, 11 samples display limited ?26Mg variations from ?0.36 to ?0.17 , similar to those of their protoliths. The mineral separates exhibit very different ?26Mg 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 = ?26Mgclinopyroxene -?26Mggarnet) varies from 1.05 to 2.15 . The clinopyroxene -garnet O isotope fractionation (?18Oclinopyroxene -garnet = ?18Oclinopyroxene -?18Ogarnet) 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 ?26Mgclinopyroxene versus ?26Mggarnet 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) Χ 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.
Abstract: Harzburgites with high modal orthopyroxene (generally >23?vol%) in Archean craton, mantle wedge and oceanic lithospheric mantle are considered to be produced by the interaction between Si-rich liquids and rocks. However, the absence of samples from continental margin hinders the recognition whether this process is prevalent. Mantle xenoliths entrained in Miocene basalts from the Thrace Basin, the margin of Eurasian continent, are dominated by harzburgites with anomalously high orthopyroxene modes. These orthopyroxene grains closely associate with spinel and occasionally with clinopyroxene. In these orthopyroxene-spinel associations, orthopyroxene grains can be up to 1?cm in diameter and display high Al2O3 contents (1.41-4.61?wt%) and Mg# values (89.6-92.4), while spinel crystals are anhedral and bud-shaped and are commonly foliated, with a wide variation in Cr# values ranging from 7.8 to 52.7. The Fe2+/Fe3+ vs. TiO2 diagram shows lots of these spinels are magmatic (i.e. spinel crystallized from melts). The orthopyroxene grains have LREE diverging from the modelled melting trends, indicating possible metasomatism following partial melting. They are present in elongated shape, cutting across olivine grains and also replacing olivine as surrounding rims. Fine-grained olivine is occasionally enclosed in the orthopyroxene-spinel association. We, therefore, propose that the association of orthopyroxene and spinel developed from the melt/fluid-rock interaction. These features indicate mineral phase transformation from olivine to orthopyroxene, which can be expressed by the equation: Mg2SiO4 (Ol)?+?SiO2?=?Mg2Si2O6 (Opx). The observed Al-rich rim of spinel and bud-shaped Al-spinel, suggest sufficient amount of Al in the Si-rich liquids. The mechanism involved here is the consumption of olivine to produce orthopyroxene and spinel as in the equation: Mg2SiO4 (Ol)?+?Al2O3?=?MgSiO3 (Opx)?+?MgAl2O4 (Sp). The Si and Al were enriched in the percolating liquids. Both the high-Cr# and low-Cr# spinels with magmatic features imply the percolating liquids were multi-staged or inhomogeneous Cr contents in the liquids. This melt/fluid-rock interaction may account for the formation of abundant harzburgites with high orthopyroxene modes in the Eurasian continental margin. Thus, it indicates the reacting harzburgites are prevalent in the lithospheric mantle beneath oceanic crust, Archean craton and mantle wedge, as well as in the continental margin.
Abstract: Harzburgites with high modal orthopyroxene (generally >23?vol%) in Archean craton, mantle wedge and oceanic lithospheric mantle are considered to be produced by the interaction between Si-rich liquids and rocks. However, the absence of samples from continental margin hinders the recognition whether this process is prevalent. Mantle xenoliths entrained in Miocene basalts from the Thrace Basin, the margin of Eurasian continent, are dominated by harzburgites with anomalously high orthopyroxene modes. These orthopyroxene grains closely associate with spinel and occasionally with clinopyroxene. In these orthopyroxene-spinel associations, orthopyroxene grains can be up to 1?cm in diameter and display high Al2O3 contents (1.41-4.61?wt%) and Mg# values (89.6-92.4), while spinel crystals are anhedral and bud-shaped and are commonly foliated, with a wide variation in Cr# values ranging from 7.8 to 52.7. The Fe2+/Fe3+ vs. TiO2 diagram shows lots of these spinels are magmatic (i.e. spinel crystallized from melts). The orthopyroxene grains have LREE diverging from the modelled melting trends, indicating possible metasomatism following partial melting. They are present in elongated shape, cutting across olivine grains and also replacing olivine as surrounding rims. Fine-grained olivine is occasionally enclosed in the orthopyroxene-spinel association. We, therefore, propose that the association of orthopyroxene and spinel developed from the melt/fluid-rock interaction. These features indicate mineral phase transformation from olivine to orthopyroxene, which can be expressed by the equation: Mg2SiO4 (Ol)?+?SiO2?=?Mg2Si2O6 (Opx). The observed Al-rich rim of spinel and bud-shaped Al-spinel, suggest sufficient amount of Al in the Si-rich liquids. The mechanism involved here is the consumption of olivine to produce orthopyroxene and spinel as in the equation: Mg2SiO4 (Ol)?+?Al2O3?=?MgSiO3 (Opx)?+?MgAl2O4 (Sp). The Si and Al were enriched in the percolating liquids. Both the high-Cr# and low-Cr# spinels with magmatic features imply the percolating liquids were multi-staged or inhomogeneous Cr contents in the liquids. This melt/fluid-rock interaction may account for the formation of abundant harzburgites with high orthopyroxene modes in the Eurasian continental margin. Thus, it indicates the reacting harzburgites are prevalent in the lithospheric mantle beneath oceanic crust, Archean craton and mantle wedge, as well as in the continental margin.
Abstract: A drastically altered chemistry was recently discovered in the Fe-O-H system under deep Earth conditions, involving the formation of iron superoxide (FeO2Hx with x?=?0 to 1), but the puzzling crystal chemistry of this system at high pressures is largely unknown. Here we present evidence that despite the high O/Fe ratio in FeO2Hx, iron remains in the ferrous, spin-paired and non-magnetic state at 60-133?GPa, while the presence of hydrogen has minimal effects on the valence of iron. The reduced iron is accompanied by oxidized oxygen due to oxygen-oxygen interactions. The valence of oxygen is not -2 as in all other major mantle minerals, instead it varies around -1. This result indicates that like iron, oxygen may have multiple valence states in our planets interior. Our study suggests a possible change in the chemical paradigm of how oxygen, iron, and hydrogen behave under deep Earth conditions.
Abstract: The North China Craton (NCC) is an atypical ancient landmass that suffered lithospheric destruction. Previous studies suggest that the eastern part of the lithospheric mantle of the NCC has been thinned and modified in the Mesozoic. However, the initiation time and mechanism of the destruction remain controversial. Mafic magmatismcould provide a unique windowinto deciphering the lithospheric mantle composition and its evolution. Here we present geochemical and geochronological data of the diamond-bearing alkaline basalts from Lan'gan, located in the southeastern margin of the NCC. Zircon U-Pb dating yielded an average age of 174 ± 14 Ma, representing the first reported Jurassic basalts in the eastern NCC. The Lan'gan basalts are enriched in light rare earth elements (LREE) and large ion lithosphile elements (LILE). Sr-Nd-Pb-Hf isotopic compositions (87Sr/86Sr(t) = 0.70646-0.70925, ?Nd(t) = ?2.1 to ?4.9, 206Pb/204Pb(t) = 17.14-18.12, 207Pb/204Pb(t) = 15.28-15.61, 208Pb/204Pb(t) = 37.82-38.67, and zircon ?Hf(t) = ?17 to ?21) are enriched compared to depleted mantle. The presence of primary amphibole indicates that the magma source of the basalts was water enriched. These observations suggest that, the lithospheric mantle of the eastern NCC were significantly refertilized, likely by slab derived fluids/melts fromthe Paleo-Pacific subduction. Owing to the Paleo-Pacific subduction, the lithosphericmantle of the eastern NCCwere reduced in viscosity and intensity, and finally promoted partialmelting in a limited scale to generate the investigated alkaline basalts. Hence, the discovery of diamond in the Lan'gan basalts demonstrates that the lithosphere of the NCC remained thick, and that large-scale destruction had not initiated in the early Jurassic beneath this region.
Abstract: The North China Craton (NCC) is an atypical ancient landmass that suffered lithospheric destruction. Previous studies suggest that the eastern part of the lithospheric mantle of the NCC has been thinned and refertilized in the Mesozoic. However, the initiation time and mechanism of the destruction remain controversial. Mafic magmatism could provide a unique window into deciphering the lithospheric mantle composition and its evolution. Here we present geochemical and geochronological data of the diamond-bearing alkaline basalts from Lan'gan, located in the southeastern margin of the NCC. Zircon UPb dating yielded an average age of 174?±?14?Ma, representing the first reported Jurassic basalts in the eastern NCC. The Lan'gan basalts are enriched in light rare earth elements (LREE) and large ion lithosphile elements (LILE). Sr-Nd-Pb-Hf isotopic compositions (87Sr/86Sr(t)?=?0.70646-0.70925, ?Nd(t)?=??2.1 to ?4.9, 206Pb/204Pb(t)?=?17.14-18.12, 207Pb/204Pb(t)?=?15.28-15.61, 208Pb/204Pb(t)?=?37.82-38.67, and zircon ?Hf(t)?=??17 to ?21) are slightly enriched compared to depleted mantle. The presence of primary amphibole indicates that the magma source of the basalts was water enriched. These observations suggest that, the lithospheric mantle of the eastern NCC were significantly refertilized, likely by slab derived fluids/melts from the Paleo-Pacific subduction. Owing to the Paleo-Pacific subduction, the lithospheric mantle of the eastern NCC were reduced in viscosity and intensity, and finally promoted partial melting in a limited scale to generate the investigated alkaline basalts. Hence, the discovery of diamond in the Lan'gan basalts demonstrates that the lithosphere of the NCC remained thick, and that large-scale destruction had not initiated in the early Jurassic beneath this region.
Geochimica et Cosmochimica Acta, Vol. 294, pp. 215-231. pdf
Mantle
bridgmanite
Abstract: The isotopic compositions of iron in major mantle minerals may record chemical exchange between deep-Earth reservoirs as a result of early differentiation and ongoing plate tectonics processes. Bridgmanite (Bdg), the most abundant mineral in the Earths lower mantle, can incorporate not only Al but also Fe with different oxidation states and spin states, which in turn can influence the distribution of Fe isotopes between Bdg and ferropericlase (Fp) and between the lower mantle and the core. In this study, we combined first-principles calculations with high-pressure nuclear resonant inelastic X-ray scattering measurements to evaluate the effects of Fe site occupancy, valence, and spin states at lower-mantle conditions on the reduced Fe partition function ratio (?-factor) of Bdg. Our results show that the spin transition of octahedral-site (B-site) Fe3+ in Bdg under mid-lower-mantle conditions generates a +0.09 increase in its ?-factor, which is the most significant effect compared to Fe site occupancy and valence. Fe2+-bearing Bdg varieties have smaller ?-factors relative to Fe3+-bearing varieties, especially those containing B-site Fe3+. Our models suggest that Fe isotopic fractionation between Bdg and Fp is only significant in the lowermost mantle due to the occurrence of low-spin Fe2+ in Fp. Assuming early segregation of an iron core from a deep magma ocean, we find that neither core formation nor magma ocean crystallization would have resulted in resolvable Fe isotope fractionation. In contrast, Fe isotopic fractionation between low-spin Fe3+-bearing Bdg/Fe2+-bearing Fp and metallic iron at the core-mantle boundary may have enriched the lowermost mantle in heavy Fe isotopes by up to +0.20.
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.
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 Earths geotherm in the Archean and the Early Proterozoic era, before ~1.4 Ga ago. Therefore, the mantle should have been severely decarbonated early in Earths 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.
Journal of Asian Earth Sciences, Vol. 214, 104772, 8p. Pdf
Mantle
carbon
Abstract: The temperature of the upper mantle was a principal factor controlling the style of plate tectonics and influencing magmatism and metamorphism on Earth over geological history. Recent studies emphasized that Earths tectonic style has transited into the modern plate tectonics since the late Neoproterozoic, which is characterized by a global network of plate boundaries with deep and cold oceanic plate subduction. However, the consequence of the establishment of modern plate tectonics to Earths mantle temperature and deep carbon cycle has not been fully understood. Here we apply statistical analysis on the geochemical data of continental igneous rocks and identify an increased magnitude of nephelinitic volcanism at the end of the Ediacaran. Nephelinitic rocks, a silica-undersaturated high-alkaline rock group, are mostly formed by low-degree melting of carbonated mantle sources. We link their widespread emergence with an enhanced mantle cooling event and a dramatically increased flux of crustal carbonates transporting to the mantle. The rapid cooling of the mantle was ascribed to the onset of modern-style plate tectonics with global-scale cold oceanic and continental subduction since the late Neoproterozoic. The declined upper-mantle temperature could not only favor the low-degree melting but also allow the subduction of carbonates into the deep mantle without decarbonation at shallow depth. Considering the high oxygen fugacity feature of the nephelinitic rocks and some other high-alkaline volcanism, the establishment of modern plate tectonics and thereafter enhanced mantle cooling and deep carbon cycle might contribute to the high-level atmospheric oxygen content during the Phanerozoic.
Zhao, Z., Niu, Y., Christensen, N.I., Zhou, W., Hou, Q., Zhang, Z.M., Xie, H., Zhang, Z.C., Liu, J.
Delamination and ultradeep subduction of continental crust: constraints from elastic wave velocity and density measurement in ultrahigh pressure met. rocks
Journal of Metamorphic Geology, Vol. 29, 7, pp. 781-801.
Sommer, H., Wan,Y., Kroner, A., Xie, H., Jacob, D.E.
Shrimp zircon ages and petrology of lower crustal granulite xenoliths from the Letseng-La-Terae kimberlite, Lesotho: further evidence for a Namaquanatal connection.
South Africa Journal of Geology, Vol. 116, 2, pp. 183-198.
Abstract: The question of whether high-grade metamorphism and crustal melting in the early Archaean were associated with modern-style plate tectonics is a major issue in unravelling early Earth crustal evolution, and the eastern Kaapvaal craton has featured prominently in this debate. We discuss a major ca. 3.2?Ga tectono-magmatic-metamorphic event in the Ancient Gneiss Complex (AGC) of Swaziland, a multiply deformed medium- to high-grade terrane in the eastern Kaapvaal craton consisting of 3.66-3.20?Ga granitoid gneisses and infolded greenstone remnants, metasedimentary assemblages and mafic dykes. We report on a 3.2?Ga granulite-facies assemblage in a metagabbro of the AGC of central Swaziland and relate this to a major thermo-magmatic event that not only affected the AGC but also the neighbouring Barberton granitoid-greenstone terrane. Some previous models have related the 3.2?Ga event in the eastern Kaapvaal craton to subduction processes, but we see no evidence for long, narrow belts and metamorphic facies changes reflecting lithospheric suture zones, and there is no unidirectional asymmetry in the thermal structure across the entire region from Swaziland to the southern Barberton granite-greenstone terrane as is typical of Phanerozoic and Proterozoic belts. Instead, we consider an underplating event at ca. 3.2?Ga, giving rise to melting in the lower crust and mixing with mantle-derived under- and intraplated mafic magma to generate the voluminous granitoid assemblages now observed in the AGC and the southern Barberton terrane. This is compatible with large-scale crustal reworking during a major thermo-magmatic event and the apparent lack of a mafic lower crust in the Kaapvaal craton as shown by seismic data.
Abstract: Magnesium and oxygen are critical elements in the solid Earth and hydrosphere. A better understanding of the combined behavior of Mg and O isotopes will refine their use as a tracer of geochemical processes and Earth evolution. In this study, the Mg-isotope compositions of garnet and omphacite separated from well-characterized xenolithic eclogites from the Roberts Victor kimberlite pipe (South Africa) have been measured by solution multi-collector ICP-MS. The reconstructed whole-rock ?26Mg values of Type I (metasomatized) eclogites range from ? 0.61 to ? 0.20 (Type IA) and from ? 0.60 to ? 0.30 (Type IB) (mean ? 0.43 ± 0.12), while ?26Mg of Type IIA (fresh, least metasomatized) eclogites ranges from ? 1.09 to ? 0.17 (mean ? 0.69 ± 0.41); a Type IIB (fresh, least metasomatized) has ?26Mg of ? 0.37. Oxygen-isotope compositions of garnet were analyzed in situ by SIMS (CAMECA 1280) and cross-checked by laser fluorination. Garnets have ?18O of 6.53 to 9.08 in Type IA, 6.14 to 6.65 in Type IB, and 2.34 to 2.91 in Type IIB. The variation of ?26Mg and ?18O in Type IA and IB eclogites is consistent with the previously proposed model for the evolution of these samples, based on major and trace elements and radiogenic isotopes. In this model, the protoliths (Type II eclogites) were metasomatized by carbonatitic to kimberlitic melts/fluids to produce first Type IA eclogites and then Type IB. Metasomatism has changed the O-isotope compositions, but the Mg-isotope compositions of Type IA are mainly controlled by the protoliths; those of Type IB eclogites reflect mixing between the protoliths and the kimberlitic melt/fluid. The combination of a large range of ?26Mg and low ?18O in Type II eclogites cannot be explained easily by seawater alteration of oceanic crust, interaction of carbonate/silicate sediments with oceanic crust, or partial melting of mafic rocks.
Abstract: Thermochemical heterogeneities detected today in the Earths mantle could arise from ongoing partial melting in different mantle regions. A major open question, however, is the level of chemical stratification inherited from an early magma-ocean (MO) solidification. Here we show that the MO crystallized homogeneously in the deep mantle, but with chemical fractionation at depths around 1000?km and in the upper mantle. Our arguments are based on accurate measurements of the viscosity of melts with forsterite, enstatite and diopside compositions up to ~30?GPa and more than 3000?K at synchrotron X-ray facilities. Fractional solidification would induce the formation of a bridgmanite-enriched layer at ~1000?km depth. This layer may have resisted to mantle mixing by convection and cause the reported viscosity peak and anomalous dynamic impedance. On the other hand, fractional solidification in the upper mantle would have favored the formation of the first crust.
Journal of Analytical At. Spectrometry, Vol. 33, pp. 231-239.
United States, Arkansas, China, Hebei, Russia, Kola Peninsula, Europe, Sweden, Canada, Ontario
geochronology
Abstract: We report the first U-Pb geochronological investigation of schorlomite garnet from carbonatite and alkaline complexes and demonstrate its applicability for U-Pb age determination using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) due to its relatively high U and Th abundances and negligible common Pb content. The comparative matrix effects of laser ablation of zircon and schorlomite are investigated and demonstrate the necessity of a suitable matrix-matched reference material for schorlomite geochronology. Laser-induced elemental fractional and instrumental mass discrimination were externally-corrected using an in house schorlomite reference material (WS20) for U-Pb geochronology. In order to validate the effectiveness and robustness of our analytical protocol, we demonstrate the veracity of U-Pb age determination for five schorlomite samples from: the Magnet Cove complex, Arkansas (USA); the Fanshan ultrapotassic complex, Hebei (China); the Ozernaya alkaline ultramafic complex, Kola Peninsula (Russia); the Alnφ alkaline-rock carbonatite complex (Sweden); and the Prairie Lake carbonatite complex, Ontario (Canada). The schorlomite U-Pb ages range from 96 Ma to 1160 Ma, and are almost identical to ages determined from other accessory minerals in these complexes and support the reliability of our analytical protocol. Schorlomite garnet U-Pb geochronology is considered to be a promising new technique for understanding the genesis of carbonatites, alkaline rocks, and related rare-metal deposits.
Geostandards and Geoanalltical Research, Vol. 43, 3, pp. 543-565.
China, Europe, Sweden, Asia, Mongolia, United States, Africa, Malawi, Madagascar
REE
Abstract: Bastnδsite is the end member of a large group of carbonate-fluoride minerals with the common formula (REE) CO3FCaCO3. This group is generally widespread and, despite never occurring in large quantities, represents the major economic light rare earth element (LREE) mineral in deposits related to carbonatite and alkaline intrusions. Since bastnδsite is easily altered and commonly contains inclusions of earlier?crystallised minerals, in situ analysis is considered the most suitable method to measure its U?Th?Pb and Sr?Nd isotopic compositions. Electron probe microanalysis and laser ablation (multi?collector) inductively coupled plasma?mass spectrometry of forty?six bastnδsite samples from LREE deposits in China, Pakistan, Sweden, Mongolia, USA, Malawi and Madagascar indicate that this mineral typically has high Th and LREE and moderate U and Sr contents. Analysis of an in?house bastnδsite reference material (K?9) demonstrated that precise and accurate U?Th?Pb ages could be obtained after common Pb correction. Moreover, the Th?Pb age with its high precision is preferable to the U?Pb age because most bastnδsites have relatively high Th rather than U contents. These results will have significant implications for understanding the genesis of endogenous ore deposits and formation processes related to metallogenic geochronology research.
Abstract: Aillikites are carbonate-rich ultramafic lamprophyres, and although they are volumetrically minor components of large igneous province (LIP), these rocks provide important clues to melting and meta-somatism in the deep mantle domain during the initial stages of LIPs. In this study, we investigate the Wajilitag kimberlites in the northwestern part of the Tarim LIP that we redefine as hypabyssal aillikites based on the following features: (1) micro-phenocrystic clinopyroxene and Ti-rich andradite garnet occurring in abundance in the carbonate-rich matrix; (2) Cr-spinel exhibiting typical Fe-Ti enrichment trend also known as titanomagnetite trend; and (3) olivine showing dominantly low Mg values (Fo < 90). To constrain the magma source and evolution, the major, minor, and trace element abundance in olivine grains from these rocks were analyzed using electron microprobe and laser ablation-inductively coupled plasma-mass spectrometry. Olivine in the aillikites occurs as two textural types: (1) groundmass olivines, as sub-rounded grains in matrix, and (2) macrocrysts, as euhedral-anhedral crystals in nodules. The groundmass olivines show varying Mg (Fo89-80) with high-Ni (1606-3418 ppm) and Mn (1424-2860 ppm) and low-Ca (571-896 ppm) contents. In contrast, the macrocrysts exhibit a restricted Fo range but a wide range in Ni and Mn. The former occurs as phenocrysts, whereas the latter are cognate cumulates that formed from earlier, evolved aillikite melt. The two olivine populations can be further divided into sub-groups, indicating a multi-stage crystallization history of the aillikite melt. The crystallization temperatures of groundmass olivines and macrocrysts in dunite nodules as computed from the spinel-olivine thermometers are 1005-1136 and 906-1041 °C, respectively. The coupled enrichment of Ca and Ti and lack of correlation between Ni and Sc and Co in the olivine grains suggest a carbonate-silicate metasomatized mantle source. Moreover, the high 100Mn/Fe (average 1.67) at high Ni (up to 3418 ppm), overlapping with OIB olivine, and the 100Ni/Mg (~1) of primitive Mg-Ni-rich groundmass olivines suggest a mixed source that involved phlogopite- and carbonate-rich metasomatic veins within mantle peridotite.
Environmental Forensics, Vol. 22, 3-4, pp. 340-350. abstract only
China
synthetics
Abstract: In this study, soil and sediment samples along with groundwater samples were collected and analyzed from an abandoned synthetic diamond production plant in Anhui Province, South China. Chemical analysis, pollution characteristics analysis, and correlation analysis were conducted to assess and to determine the source(s) of the toxic metal and organic pollutions in the study sites. The Co and Ni concentrations of soil samples collected from the production area exceed the risk screening value for contaminated development land in Soil Environment Quality Standards for soil pollution risk control on construction land (Trial) of China, while the concentrations of other toxic elements such as Cr, Cu, and Zn are lower than the screening value. The PCA and HCA results are consistent with the correlation coefficient analysis and indicate that industrial activities are the main sources of Co and Ni. The chemical composition and source analysis results of soil and groundwater show that toxic metals originating from catalyst and low pH value from acid waste water should be the main point of concern in the synthetic diamond production plant.
Abstract: Maohokite, a post?spinel polymorph of MgFe2O4, was found in shocked gneiss from the Xiuyan crater in China. Maohokite in shocked gneiss coexists with diamond, reidite, TiO2?II, as well as diaplectic glasses of quartz and feldspar. Maohokite occurs as nano?sized crystallites. The empirical formula is (Mg0.62Fe0.35Mn0.03)2+Fe3+2O4. In situ synchrotron X?ray microdiffraction established maohokite to be orthorhombic with the CaFe2O4?type structure. The cell parameters are a = 8.907 (1) Ε, b = 9.937(8) Ε, c = 2.981(1) Ε; V = 263.8 (3) Ε3; space group Pnma. The calculated density of maohokite is 5.33 g cm?3. Maohokite was formed from subsolidus decomposition of ankerite Ca(Fe2+,Mg)(CO3)2 via a self?oxidation?reduction reaction at impact pressure and temperature of 25-45 GPa and 800-900 °C. The formation of maohokite provides a unique example for decomposition of Fe?Mg carbonate under shock?induced high pressure and high temperature. The mineral and its name have been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA 2017?047). The mineral was named maohokite after Hokwang Mao, a staff scientist at the Geophysical Laboratory, Carnegie Institution of Washington, for his great contribution to high pressure research.
Environmental Forensics, Vol. 22, 3-4, pp. 340-350. abstract only
China
synthetics
Abstract: In this study, soil and sediment samples along with groundwater samples were collected and analyzed from an abandoned synthetic diamond production plant in Anhui Province, South China. Chemical analysis, pollution characteristics analysis, and correlation analysis were conducted to assess and to determine the source(s) of the toxic metal and organic pollutions in the study sites. The Co and Ni concentrations of soil samples collected from the production area exceed the risk screening value for contaminated development land in Soil Environment Quality Standards for soil pollution risk control on construction land (Trial) of China, while the concentrations of other toxic elements such as Cr, Cu, and Zn are lower than the screening value. The PCA and HCA results are consistent with the correlation coefficient analysis and indicate that industrial activities are the main sources of Co and Ni. The chemical composition and source analysis results of soil and groundwater show that toxic metals originating from catalyst and low pH value from acid waste water should be the main point of concern in the synthetic diamond production plant.
Abstract: As the most abundant material of rocky planets, high-pressure polymorphs of iron- and aluminum-bearing magnesium silicates have long been sought by both observations and experiments. Meanwhile, it was recently revealed that iron oxides form (FeO)m(Fe2O3)n homologous series above ?10 GPa according to laboratory high-pressure experiments. Here, we report a new high-pressure iron-magnesium silicate, recently approved by the International Mineralogical Association as a new mineral (No. 2020-086) and named elgoresyite, in a shock-induced melt vein of the Suizhou L6 chondrite with a chemistry of (Mg,Fe)5Si2O9. The crystal structure of this new silicate is the same as the iron oxide Fe7O9, strongly suggesting that silicates also form ((Mg,Fe)O)m + n(SiO2)n series that are isostructural to iron oxides via (Mg2+,Fe2+) + Si4+ = 2Fe3+ substitution. To test this hypothesis, the phase relationships of the silicates and iron oxides should be further investigated at higher temperature conditions. Newly found iron-magnesium silicate is a potential constituent mineral in rocky planets with relatively high MgO + FeO content.
Reviews in Economic Geology, Vol. 18, pp. 115-136.
China
REE deposits
Abstract: China is the worlds leading rare earth element (REE) producer and hosts a variety of deposit types. Carbonatite-related REE deposits, the most significant deposit type, include two giant deposits presently being mined in China, Bayan Obo and Maoniuping, the first and third largest deposits of this type in the world, respectively. The carbonatite-related deposits host the majority of Chinas REE resource and are the primary supplier of the worlds light REE. The REE-bearing clay deposits, or ion adsorption-type deposits, are second in importance and are the main source in China for heavy REE resources. Other REE resources include those within monazite or xenotime placers, beach placers, alkaline granites, pegmatites, and hydrothermal veins, as well as some additional deposit types in which REE are recovered as by-products. Carbonatite-related REE deposits in China occur along craton margins, both in rifts (e.g., Bayan Obo) and in reactivated transpressional margins (e.g., Maoniuping). They comprise those along the northern, eastern, and southern margins of the North China block, and along the western margin of the Yangtze block. Major structural features along the craton margins provide first-order controls for REE-related Proterozoic to Cenozoic carbonatite alkaline complexes; these are emplaced in continental margin rifts or strike-slip faults. The ion adsorption-type REE deposits, mainly situated in the South China block, are genetically linked to the weathering of granite and, less commonly, volcanic rocks and lamprophyres. Indosinian (early Mesozoic) and Yanshanian (late Mesozoic) granites are the most important parent rocks for these REE deposits, although Caledonian (early Paleozoic) granites are also of local importance. The primary REE enrichment is hosted in various mineral phases in the igneous rocks and, during the weathering process, the REE are released and adsorbed by clay minerals in the weathering profile. Currently, these REE-rich clays are primarily mined from open-pit operations in southern China. The complex geologic evolution of Chinas Precambrian blocks, particularly the long-term subduction of ocean crust below the North and South China blocks, enabled recycling of REE-rich pelagic sediments into mantle lithosphere. This resulted in the REE-enriched nature of the mantle below the Precambrian cratons, which were reactivated and thus essentially decratonized during various tectonic episodes throughout the Proterozoic and Phanerozoic. Deep fault zones within and along the edges of the blocks, including continental rifts and strike-slip faults, provided pathways for upwelling of mantle material.
Abstract: Mantle-derived carbonatites provide a unique window in the understanding of mantle characteristics and dynamics, as well as insight into the assembly and breakup of supercontinents. As a petrological indicator of extensional tectonic regimes, Archean/Proterozoic carbonatites provide important constraints on the timing of the breakup of ancient supercontinents. The majority of the carbonatites reported worldwide are Phanerozoic, in part because of the difficulty in recognizing Archean/Proterozoic carbonatites, which are characterized by strong foliation and recrystallization, and share broad petrologic similarities with metamorphosed sedimentary lithologies. Here, we report the recognition of a ~1.85?Ga carbonatite in Chaihulanzi area of Chifeng in north China based on systematic geological, petrological, geochemical, and baddeleyite U-Pb geochronological results. The carbonatite occurs as dikes or sills emplaced in Archean metasedimentary rocks and underwent intense deformation. Petrological and SEM/EDS results show that calcite and dolomite are the dominant carbonate minerals along with minor and varied amounts of Mg-rich mafic minerals, including forsterite (with Fo?>?98), phlogopite, diopside, and an accessory amount of apatite, baddeleyite, spinel, monazite, and ilmenite. The relatively high silica content together with the non-arc and OIB-like trace element signatures of the carbonatite indicates a hot mantle plume as the likely magma source. The depleted Nd isotopic signatures suggest that plume upwelling might be triggered by the accumulation of recycled crust in the deep mantle. As a part of the global-scale Columbia supercontinent, the Proterozoic tectonic evolution of the North China Craton (NCC) provides important insights into the geodynamics governing amalgamation and fragmentation of the supercontinent. The Paleo-Mesoproterozoic boundary is the key point of tectonic transition from compressional to extensional settings in the NCC. The newly identified ~1.85?Ga carbonatite provides a direct link between the long-lasting supercontinental breakup and plume activity, which might be sourced from the slab graveyard, continental crustal slabs subducted into asthenosphere, beneath the supercontinent. The carbonatite provides a precise constraint of the initiation of the continental breakup at ~1.85?Ga.
Abstract: Mantle-derived carbonatites provide a unique window in the understanding of mantle characteristics and dynamics, as well as insight into the assembly and breakup of supercontinents. As a petrological indicator of extensional tectonic regimes, Precambrian carbonatites provide important constraints on the timing of the breakup of ancient supercontinents. The majority of the carbonatites reported worldwide are Phanerozoic, in part because of the difficulty in recognizing Precambrian carbonatites, which are characterized by strong foliation and recrystallization, and share broad petrologic similarities with metamorphosed sedimentary lithologies. Here we report the recognition of a ~1.85?Ga carbonatite in Chaihulanzi area of Chifeng in north China based on systematic geological, petrological, geochemical, and baddeleyite U-Pb geochronological results. The carbonatite occurs as dikes or sills emplaced in Archean metasedimentary rocks and underwent intense deformation. Petrological and SEM/EDS results show that calcite and dolomite are the dominant carbonate minerals along with minor and varied amounts of Mg-rich mafic minerals, including forsterite (with Fo?>?98), phlogopite, diopside, and an accessory amount of apatite, baddeleyite, spinel, monazite, and ilmenite. The relatively high silica content together with the non-arc and OIB-like trace element signatures of the carbonatite indicates a hot mantle plume as the likely magma source. The depleted Nd isotopic signatures suggest that plume upwelling might be triggered by the accumulation of recycled crust in the deep mantle. As a part of the global-scale Columbia supercontinent, the Proteozoic tectonic evolution of the North China Craton (NCC) provides important insights into the geodynamics governing amalgamation and fragmentation of the supercontinent. The Paleo-Mesoproterozoic boundary is the key point of tectonic transition from compressional to extensional settings in the NCC. The newly-identified ~1.85?Ga carbonatite provides a direct link between the long-lasting supercontinental breakup and plume activity, which might be sourced from the slab graveyard, continental crustal slabs subducted into asthenosphere, beneath the supercontinent. The carbonatite provides a precise constraint of the initiation of the continental breakup at ~1.85?Ga.
Abstract: Mantle-derived carbonatites provide a unique window in the understanding of mantle characteristics and dynamics, as well as insight into the assembly and breakup of supercontinents. As a petrological indicator of extensional tectonic regimes, Precambrian carbonatites provide important constraints on the timing of the breakup of ancient supercontinents. The majority of the carbonatites reported worldwide are Phanerozoic, in part because of the difficulty in recognizing Precambrian carbonatites, which are characterized by strong foliation and recrystallization, and share broad petrologic similarities with metamorphosed sedimentary lithologies. Here we report the recognition of a ~1.85?Ga carbonatite in Chaihulanzi area of Chifeng in north China based on systematic geological, petrological, geochemical, and baddeleyite U-Pb geochronological results. The carbonatite occurs as dikes or sills emplaced in Archean metasedimentary rocks and underwent intense deformation. Petrological and SEM/EDS results show that calcite and dolomite are the dominant carbonate minerals along with minor and varied amounts of Mg-rich mafic minerals, including forsterite (with Fo?>?98), phlogopite, diopside, and an accessory amount of apatite, baddeleyite, spinel, monazite, and ilmenite. The relatively high silica content together with the non-arc and OIB-like trace element signatures of the carbonatite indicates a hot mantle plume as the likely magma source. The depleted Nd isotopic signatures suggest that plume upwelling might be triggered by the accumulation of recycled crust in the deep mantle. As a part of the global-scale Columbia supercontinent, the Proteozoic tectonic evolution of the North China Craton (NCC) provides important insights into the geodynamics governing amalgamation and fragmentation of the supercontinent. The Paleo-Mesoproterozoic boundary is the key point of tectonic transition from compressional to extensional settings in the NCC. The newly-identified ~1.85?Ga carbonatite provides a direct link between the long-lasting supercontinental breakup and plume activity, which might be sourced from the slab graveyard, continental crustal slabs subducted into asthenosphere, beneath the supercontinent. The carbonatite provides a precise constraint of the initiation of the continental breakup at ~1.85?Ga.
SEG Reviews In Economic Geology Chapter 6, Vol. 18, pp. 115-136.
China
REE
Abstract: China is the worlds leading rare earth element (REE) producer and hosts a variety of deposit types. Carbonatite- related REE deposits, the most significant deposit type, include two giant deposits presently being mined in China, Bayan Obo and Maoniuping, the first and third largest deposits of this type in the world, respectively. The carbonatite-related deposits host the majority of Chinas REE resource and are the primary supplier of the worlds light REE. The REE-bearing clay deposits, or ion adsorption-type deposits, are second in importance and are the main source in China for heavy REE resources. Other REE resources include those within monazite or xenotime placers, beach placers, alkaline granites, pegmatites, and hydrothermal veins, as well as some additional deposit types in which REE are recovered as by-products. Carbonatite-related REE deposits in China occur along craton margins, both in rifts (e.g., Bayan Obo) and in reactivated transpressional margins (e.g., Maoniuping). They comprise those along the northern, eastern, and southern margins of the North China block, and along the western margin of the Yangtze block. Major structural features along the craton margins provide first-order controls for REE-related Proterozoic to Cenozoic carbonatite alkaline complexes; these are emplaced in continental margin rifts or strike-slip faults. The ion adsorption-type REE deposits, mainly situated in the South China block, are genetically linked to the weathering of granite and, less commonly, volcanic rocks and lamprophyres. Indosinian (early Mesozoic) and Yanshanian (late Mesozoic) granites are the most important parent rocks for these REE deposits, although Caledonian (early Paleozoic) granites are also of local importance. The primary REE enrichment is hosted in various mineral phases in the igneous rocks and, during the weathering process, the REE are released and adsorbed by clay minerals in the weathering profile. Currently, these REE-rich clays are primarily mined from open-pit operations in southern China. The complex geologic evolution of Chinas Precambrian blocks, particularly the long-term subduction of ocean crust below the North and South China blocks, enabled recycling of REE-rich pelagic sediments into mantle lithosphere. This resulted in the REE-enriched nature of the mantle below the Precambrian cratons, which were reactivated and thus essentially decratonized during various tectonic episodes throughout the Proterozoic and Phanerozoic. Deep fault zones within and along the edges of the blocks, including continental rifts and strike-slip faults, provided pathways for upwelling of mantle material.
Abstract: The rare earth elements (REEs) consist of the 15 lantha-nide elements (La to Lu). Because of the increasing application of REEs and yttrium (REY) in high-and green-tech industries, the demand for the REY is projected to increase in the future. Rare earth elements are relatively abundant in the Earth's crust, but discovered, minable concentrations are less common than for most other ore types. Bastnaesite and monazite are the main mineral source of REEs in the world. Bastnaesite-hosted deposits in China and the United States Abstract China has been the world's leading rare earth element (REE) and yttrium producer for more than 20 years and hosts a variety of deposit types. Carbonatite-related REE deposits are the most significant REE deposit type, with REY (REE and yttrium)-bearing clay deposits, or ion adsorption-type deposits, being the primary source of the world's heavy REEs. Other REY resources in China include those hosted in placers, alkaline granites, pegmatites, and hydrothermal veins, as well as in additional deposit types in which REEs may be recovered as by-product commodities. Carbonatite-related REE deposits in China provide nearly all the light REE production in the world. Two giant deposits are currently being mined in China: Bayan Obo and Maoniuping. The carbonatite-related REE deposits in China occur along the margins of Archean-Paleoproterozoic blocks, including the northern , southern, and eastern margins of the North China craton, and the western margin of the Yangtze craton. The carbonatites were emplaced in continental rifts (e.g., Bayan Obo) or translithospheric strike-slip faults (e.g., Maoniuping) along reactivated craton margins. The craton margins provide the first-order control for carbonatite-related REE resources. Four REE metallogenic belts, including the Proterozoic Langshan-Bayan Obo, late Paleozoic-early Mesozoic eastern Qinling-Dabie, late Mesozoic Chishan-Laiwu-Zibo, and Cenozoic Mianning-Dechang belts, occur along cratonic margins. Geologic and geochemical data demonstrate that the carbonatites in these belts originated from mantle sources that had been previously enriched, most likely by recycled marine sediments through subduction zones during the assembly of continental blocks. Although the generation of carbonatite magma is debated, a plausible mechanism is by liquid immiscibility between silicate and carbonate melts. This process would further enrich REEs in the carbonatite end member during the evolution of mantle-derived magma. The emplacement of carbonatite magma in the upper crust, channeled by translithospheric faults in extensional environments, leads to a rapid decompression of the magma and consequently exsolution of a hydrothermal fluid phase. The fluid is characterized by high temperature (600°-850°C), high pressure (up to 350 MPa), and enrichment in sulfate, CO2, K, Na, Ca, Sr, Ba, and REEs. Immiscibility of sulfate melts from the aqueous fluid, and phase separation between CO2 and water may take place upon fluid cooling. Although both sulfate and chloride have been called upon as important ligands in hydrothermal REE transport, results of our studies suggest that sulfate is more important. The exsolution of a sulfate melt from the primary carbonatite fluid would lead to a significant decrease of the sulfate activity in the fluid and trigger REE precipitation. The subsequent unmixing between CO2 and water may also play an important role in REE precipitation. Because of the substantial ability of the primary carbonatite fluid to contain REEs, a large-volume magma chamber or huge fluid flux are not necessary for the formation of a giant REE deposit. A dense carbonatite fluid and rapid evolution hinder long distance fluid transportation and distal mineralization. Thus, carbonatite-related alteration and mineralization occur in or proximal to carbonatite dikes and sills, and this is observed in all carbonatite-related REE deposits in China. Ion adsorption-type REE deposits are primarily located in the South China block and are genetically linked to the weathering of granite and, less commonly, volcanic rocks and lamprophyres. Indosinian (early Mesozoic) and Yanshanian (late Mesozoic) granites are the most important parent rocks for these REE deposits. Hydro-thermal alteration by fluids exsolved from late Mesozoic granites or related alkaline rocks (e.g., syenite) may have enriched the parent rocks in REEs, particularly the heavy REEs. Furthermore, this alteration process led to the transformation of some primary REE minerals to secondary REE minerals that are more readily broken down during subsequent weathering. During the weathering process, the REEs are released from parent rocks and adsorbed onto kaolinite and halloysite in the weathering profile, and further enriched by the loss of other material to form the ion adsorption-type REE deposits. A warm and humid climate and a low-relief landscape are important characteristics for development of ion adsorption REE deposits.
Abstract: China is the worlds leading rare earth element (REE) producer and hosts a variety of deposit types. Carbonatite- related REE deposits, the most significant deposit type, include two giant deposits presently being mined in China, Bayan Obo and Maoniuping, the first and third largest deposits of this type in the world, respectively. The carbonatite-related deposits host the majority of Chinas REE resource and are the primary supplier of the worlds light REE. The REE-bearing clay deposits, or ion adsorption-type deposits, are second in importance and are the main source in China for heavy REE resources. Other REE resources include those within monazite or xenotime placers, beach placers, alkaline granites, pegmatites, and hydrothermal veins, as well as some additional deposit types in which REE are recovered as by-products. Carbonatite-related REE deposits in China occur along craton margins, both in rifts (e.g., Bayan Obo) and in reactivated transpressional margins (e.g., Maoniuping). They comprise those along the northern, eastern, and southern margins of the North China block, and along the western margin of the Yangtze block. Major structural features along the craton margins provide first-order controls for REE-related Proterozoic to Cenozoic carbonatite alkaline complexes; these are emplaced in continental margin rifts or strike-slip faults. The ion adsorption-type REE deposits, mainly situated in the South China block, are genetically linked to the weathering of granite and, less commonly, volcanic rocks and lamprophyres. Indosinian (early Mesozoic) and Yanshanian (late Mesozoic) granites are the most important parent rocks for these REE deposits, although Caledonian (early Paleozoic) granites are also of local importance. The primary REE enrichment is hosted in various mineral phases in the igneous rocks and, during the weathering process, the REE are released and adsorbed by clay minerals in the weathering profile. Currently, these REE-rich clays are primarily mined from open-pit operations in southern China. The complex geologic evolution of Chinas Precambrian blocks, particularly the long-term subduction of ocean crust below the North and South China blocks, enabled recycling of REE-rich pelagic sediments into mantle lithosphere. This resulted in the REE-enriched nature of the mantle below the Precambrian cratons, which were reactivated and thus essentially decratonized during various tectonic episodes throughout the Proterozoic and Phanerozoic. Deep fault zones within and along the edges of the blocks, including continental rifts and strike-slip faults, provided pathways for upwelling of mantle material.
Episodic growth of zircon in UHP orthogneisses from the North Dabie Terrane of east central China: implications for crustal architecture of a collisional orogen.
Journal of Metamorphic Geology, In press available,
Delamination and ultradeep subduction of continental crust: constraints from elastic wave velocity and density measurement in ultrahigh pressure metamorphic rocks
Journal of Metamorphic Geology, Vol. 29, 7, pp. 781-801.
Studies on the defect structures and metasomatism of olivine and pryoxenein lherzolite xenoliths from basalts in Fujian and Zhejiang Provinces, southeastern China
International Mineralogical Association Meeting Held June, 1990 Beijing China, Vol. 1, extended abstract p. 363-364
Studies on the defect structures and metasomatism of olivine and pryoxenein lherzolite xenoliths from basalts in Fujian and Zhejiang Provinces, southeastern China
International Mineralogical Association Meeting Held June, 1990 Beijing China, Vol. 1, extended abstract p. 363-364
Li, L-M., Sun, M., Wang, Y., Xing, G., Zhao, G., Cai, K., Zhang, Y.
Geochronological and geochemical study of Paleproterozoic gneissic granites and clinopyroxenite xenolths from NW Fujian: implications for crustal evol.
Journal of Asian Earth Sciences, Vol. 41, 2, pp. 204-212.
Earth and Planetary Science Letters, Vol. 494, 1, pp. 92-98.
Mantle
water
Abstract: In this study, we present new experimental constraints on the phase stability and thermal equation of state of an important hydrous phase, ?-AlOOH, using synchrotron X-ray diffraction up to 142 GPa and 2500 K. Our experimental results have shown that ?-AlOOH remains stable at the whole mantle pressure-temperature conditions above the D? layer yet will decompose at the core-mantle boundary because of a dramatic increase in temperature from the silicate mantle to the metallic outer core. At the bottom transition zone and top lower mantle, the formation of ?-AlOOH by the decomposition of phase Egg is associated with a ?2.1-2.5% increase in density (?) and a ?19.7-20.4% increase in bulk sound velocity (V?). The increase in ? across the phase Egg to ?-AlOOH phase transition can facilitate the subduction of ?-AlOOH to the lower mantle. Compared to major lower-mantle phases, ?-AlOOH has the lowest ? but greatest V?, leading to an anomalous low ? /V? ratio which can help to identify the potential presence of ?-AlOOH in the region. More importantly, water released from the breakdown of ?-AlOOH at the core-mantle boundary could lower the solidus of the pyrolitic mantle to cause partial melting and/or react with Fe in the region to form the low-velocity FeO2Hx phase. The presence of partial melting and/or the accumulation of FeO2Hx phase at the CMB could be the cause for the ultra-low velocity zone. ?-AlOOH is thus an important phase to transport water to the lowermost mantle and helps to understand the origin of the ultra-low velocity zone.
Journal of Geophysical Research , Vol. 124, 5, pp. 4617-4638.
Mantle
melting
Abstract: The oxidation state of the Earth`s mantle, often expressed as oxygen fugacity (fO2), could control the behavior of multivalent elements and thus exert a significant influence on the formation of magmatic ore deposits and the secular evolution of Earth`s atmosphere. Whether arc mantle is more oxidized than oceanic mantle remains a controversial topic. As a multivalent element, partitioning behavior of vanadium is fO2 sensitive and is capable of tracking mantle redox state. However, except fO2, other factors (temperature, pressure, and phase composition) that may affect vanadium partitioning behavior have not been clearly evaluated. Here we conducted high temperature and pressure experiments to determine partition coefficients of vanadium during mantle melting under various fO2 conditions. Combining our and published data, we evaluated the effects of fO2, T, P, and compositions of mineral and melt on the vanadium partitioning using multiple linear regressions. The results indicate that, in addition to fO2, temperature exerts a significant control on the vanadium partitioning. Additionally, we estimated fO2 of the arc mantle via numerical modelling using appropriate partition coefficients for vanadium. Our results clarify and reconcile the discrepancies between previous studies and reveal that arc mantle is generally ~10 times more oxidized than oceanic mantle.
Geochronology and isotopic character of ultrahigh pressure metamorphism with implications for collision of the Sino Korean and Yangtze Cratons, centralChina.
Abstract: Diamond, moissanite and a variety of other minerals, similar to those reported from ophiolites in Tibet and northern Russia, have recently been discovered in chromitites of the Hegenshan ophiolite of the Central Asian Orogenic Belt, north China. The chromitites are small, podiform and vein-like bodies hosted in dunite, clinopyroxene-bearing peridotite, troctolite and gabbro. All of the analysed chromite grains are relatively Al-rich, with Cr# [100Cr/(Cr+Al)] of about 47-53. Preliminary studies of mainly disseminated chromitite from ore body No. 3756 have identified more than 30 mineral species in addition to diamond and moissanite. These include oxides (mostly hematite, magnetite, rutile, anatase, cassiterite, and quartz), sulfides (pyrite, marcasite and others), silicates (magnesian olivine, enstatite, augite, diopside, uvarovite, pyrope, orthoclase, zircon, sphene, vesuvianite, chlorite and serpentine) and others (e.g., calcite, monazite, glauberite, iowaite and a range of metallic alloys). This study demonstrates that diamond, moissanite and other exotic minerals can occur in high-Al, as well as high-Cr chromites, and significantly extends the geographic and age range of known diamond-bearing ophiolites.
Abstract: Various combinations of diamond, moissanite, zircon, quartz, corundum, rutile, titanite, almandine garnet, kyanite, and andalusite have been recovered from the Dangqiong peridotites. More than 80 grains of diamond have been recovered, most of which are pale yellow to reddish-orange to colorless. The grains are all 100-200 ΅m in size and mostly anhedral, but with a range of morphologies including elongated, octahedral and subhedral varieties. Their identification was confirmed by a characteristic shift in the Raman spectra between 1325 cm?1 and 1333 cm?1, mostly at 1331.51 cm?1 or 1326.96 cm?1. Integration of the mineralogical, petrological and geochemical data for the Dongqiong peridotites suggests a multi-stage formation for this body and similar ophiolites in the Yarlung-Zangbo suture zone. Chromian spinel grains and perhaps small bodies of chromitite crystallized at various depths in the upper mantle, and encapsulated the UHP, highly reduced and crustal minerals. Some oceanic crustal slabs containing the chromian spinel and their inclusion were later trapped in suprasubduction zones (SSZ), where they were modified by island arc tholeiitic and boninitic magmas, thus changing the chromian spinel compositions and depositing chromitite ores in melt channels.
Abstract: Various combinations of diamond, moissanite, zircon, corundum, rutile and titanitehave been recovered from the Bulqiza chromitites. More than 10 grains of diamond have been recovered, most of which are pale yellow to reddishorange to colorless. The grains are all 100300 ?m in size and mostly anhedral, but with a range of morphologies including elongated, octahedral and subhedral varieties. Their identification was confirmed by a characteristic shift in the Raman spectra between 1325 cm?1 and 1333 cm?1, mostly at 1331.51 cm?1 or 1326.96 cm?1. This investigation extends the occurrence of diamond and moissanite to the Bulqiza chromitites in the Eastern Mirdita Ophiolite. Integration of the mineralogical, petrological and geochemical data of the Bulqiza chromitites suggests their multistage formation. Magnesiochromite grains and perhaps small bodies of chromitite formed at various depths in the upper mantle, and encapsulated the ultrahigh pressure, highly reduced and crustal minerals. Some oceanic crustal slabs containing the magnesiochromite and their inclusion were later trapped in suprasubduction zones, where they were modified by tholeiitic and boninitic arc magmas, thus changing the magnesiochromite compositions and depositing chromitite ores in melt channels.
Abstract: The Pozanti-Karsanti ophiolite situated in the eastern Tauride belt, southern Turkey, is a well-preserved oceanic lithosphere remnant comprising, in ascending order, mantle peridotite, ultramafic and mafic cumulates, isotropic gabbros, sheeted dikes, and basaltic pillow lavas. Two types of chromitites are observed in the Pozanti-Karsanti ophiolite. One type of chromitites occurs in the cumulate dunites around the Moho, and the other type of chromitites is hosted by the mantle harzburgites below the Moho. The second type of chromitites has massive, nodular, and disseminated textures. We have conducted the mineral separation work on the podiform chromitites hosted by harzburgites. So far, more than 100 grains of microdiamond and moissanite (SiC) have been recovered from the podiform chromitite. The diamonds and moissanite are accompanied by large amounts of rutile. Besides zircon, monazite and sulfide are also very common phases within the separated minerals. The discovery of diamond, moissanite, and the other unusual minerals from podiform chromitite of the Pozanti-Karsanti ophiolite provides new evidences for the common occurrences of these unusual minerals in ophiolitic peridotites and chromitites. This discovery also suggests that deep mantle processes and materials have been involved in the formation of podiform chromitite.
Journal of Asian Earth Sciences, Vol. 159, pp. 109-129.
China, Tibet
chromitites
Abstract: The Purang harzburgite massif in SW Tibet (China) hosts abundant chrome ore deposits. Ores consist of 20 to >95% modal chromian spinel (Cr-spinel) with mylonitic fabric in imbricate shaped pods. The composition of Cr-spinel in these ores ranges from Al-rich [Cr#Sp or Cr/(Cr?+?Al)?Χ?100?=?47.60-57.56] to Cr-rich (Cr#Sp: 62.55-79.57). Bulk platinum-group element (PGE) contents of chromitites are also highly variable ranging from 17.5?ppb to ?2.5?ppm. Both metallurgical and refractory chromitites show a general enrichment in the IPGE (Os, Ir and Ru) with respect to the PPGE (Rh, Pt and Pd), resulting mostly in right-sloping primitive mantle (PM)-normalized PGE profiles. The platinum-group mineral (PGM) assemblages of both chromitite types are dominated by heterogeneously distributed, euhedral Os-bearing laurite inclusions in Cr-spinel. The Purang chromitites have quite inhomogeneous 187Os/188Os ratios (0.12289-0.13194) that are within the range of those reported for mantle-hosted chromitites from other peridotite massifs. Geochemical calculations demonstrate that the parental melts of high-Cr chromitites were boninitic, whereas those of high-Al chromitites had an arc-type tholeiitic affinity. Chromite crystallization was most likely stimulated by changes in magma compositions due to melt-peridotite interaction, leading to the establishment of a heterogeneous physicochemical environment during the early crystallization of the PGM. The highly variable PGE contents, inhomogeneous Os-isotopic compositions and varying Cr#Sp ratios of these chromitites imply a polygenetic origin for them from spatially distinct melt inputs. The generally low ?Os values (<1) of chromitites indicate that their parental melts originated within different sections of a heterogeneously depleted mantle source region. These melts were most likely produced in the mantle wedge above a downgoing lithospheric slab.
Abstract: We report new ?13C ?values data and N?content and N?aggregation state values for microdiamonds recovered from peridotites and chromitites of the Luobusa ophiolite (Tibet) and chromitites of the Ray?Iz ophiolite in the Polar Urals (Russia). All analyzed microdiamonds contain significant nitrogen contents (from 108 up to 589 ± 20% atomic ppm) with a consistently low aggregation state, show identical IR spectra dominated by strong absorption between 1130 cm?1 and 1344 cm?1, and hence characterize Type Ib diamond. Microdiamonds from the Luobusa peridotites have ?13C ?PDB?values ranging from ?28.7 to ?16.9, and N?contents from 151 to 589 atomic ppm. The ?13C and N?content values for diamonds from the Luobusa chromitites are ?29 to ?15.5 and 152 to 428 atomic ppm, respectively. Microdiamonds from the Ray?Iz chromitites show values varying from ?27.6 to ?21.6 in ?13C and from 108 to 499 atomic ppm in N. The carbon isotopes values bear similar features with previously analyzed metamorphic diamonds from other worldwide localities, but the samples are characterized by lower N?contents. In every respect, they are different from diamonds occurring in kimberlites and impact craters. Our samples also differ from the few synthetic diamonds; we also analyzed showing enhanced ?13C ?variability and less advanced aggregation state than synthetic diamonds. Our newly obtained N?aggregation state and N?content data are consistent with diamond formation over a narrow and rather cold temperature range (i.e. <950°C), and in a short residence time (i.e. within several million years) at high temperatures in the deep mantle.
Abstract: Diamonds have been discovered in mantle peridotites and chromitites of six ophiolitic massifs along the 1300 km?long Yarlung?Zangbo suture (Bai et al., 1993; Yang et al., 2014; Xu et al., 2015), and in the Dongqiao and Dingqing mantle peridotites of the Bangong?Nujiang suture in the eastern Tethyan zone (Robinson et al., 2004; Xiong et al., 2018). Recently, in?situ diamond, coesite and other UHP mineral have also been reported in the Nidar ophiolite of the western Yarlung?Zangbo suture (Das et al., 2015, 2017). The above?mentioned diamond?bearing ophiolites represent remnants of the eastern Mesozoic Tethyan oceanic lithosphere. New publications show that diamonds also occur in chromitites in the Pozanti?Karsanti ophiolite of Turkey, and in the Mirdita ophiolite of Albania in the western Tethyan zone (Lian et al., 2017; Xiong et al., 2017; Wu et al., 2018). Similar diamonds and associated minerals have also reported from Paleozoic ophiolitic chromitites of Central Asian Orogenic Belt of China and the Ray?Iz ophiolite in the Polar Urals, Russia (Yang et al., 2015a, b; Tian et al., 2015; Huang et al, 2015). Importantly, in?situ diamonds have been recovered in chromitites of both the Luobusa ophiolite in Tbet and the Ray?Iz ophiolite in Russia (Yang et al., 2014, 2015a). The extensive occurrences of such ultra?high pressure (UHP) minerals in many ophiolites suggest formation by similar geological events in different oceans and orogenic belts of different ages. Compared to diamonds from kimberlites and UHP metamorphic belts, micro?diamonds from ophiolites present a new occurrence of diamond that requires significantly different physical and chemical conditions of formation in Earth's mantle. The forms of chromite and qingsongites (BN) indicate that ophiolitic chromitite may form at depths of >150?380 km or even deeper in the mantle (Yang et al., 2007; Dobrthinetskaya et al., 2009). The very light C isotope composition (?13C ?18 to ?28) of these ophiolitic diamonds and their Mn?bearing mineral inclusions, as well as coesite and clinopyroxene lamallae in chromite grains all indicate recycling of ancient continental or oceanic crustal materials into the deep mantle (>300 km) or down to the mantle transition zone via subduction (Yang et al., 2014, 2015a; Robinson et al., 2015; Moe et al., 2018). These new observations and new data strongly suggest that micro?diamonds and their host podiform chromitite may have formed near the transition zone in the deep mantle, and that they were then transported upward into shallow mantle depths by convection processes. The in?situ occurrence of micro?diamonds has been well?demonstrated by different groups of international researchers, along with other UHP minerals in podiform chromitites and ophiolitic peridotites clearly indicate their deep mantle origin and effectively address questions of possible contamination during sample processing and analytical work. The widespread occurrence of ophiolite?hosted diamonds and associated UHP mineral groups suggests that they may be a common feature of in?situ oceanic mantle. The fundamental scientific question to address here is how and where these micro?diamonds and UHP minerals first crystallized, how they were incorporated into ophiolitic chromitites and peridotites and how they were preserved during transport to the surface. Thus, diamonds and UHP minerals in ophiolites have raised new scientific problems and opened a new window for geologists to study recycling from crust to deep mantle and back to the surface.
International Symposium on Deep Earth Exploration and Practices, Beijing Oct. 24-26. 1 p. abstract
China
diamond genesis
Abstract: Diamonds have been discovered in mantle peridotites and chromitites of six ophiolitic massifs along the 1300 km?long Yarlung?Zangbo suture (Bai et al., 1993; Yang et al., 2014; Xu et al., 2015), and in the Dongqiao and Dingqing mantle peridotites of the Bangong?Nujiang suture in the eastern Tethyan zone (Robinson et al., 2004; Xiong et al., 2018). Recently, in?situ diamond, coesite and other UHP mineral have also been reported in the Nidar ophiolite of the western Yarlung?Zangbo suture (Das et al., 2015, 2017). The above?mentioned diamond?bearing ophiolites represent remnants of the eastern Mesozoic Tethyan oceanic lithosphere. New publications show that diamonds also occur in chromitites in the Pozanti?Karsanti ophiolite of Turkey, and in the Mirdita ophiolite of Albania in the western Tethyan zone (Lian et al., 2017; Xiong et al., 2017; Wu et al., 2018). Similar diamonds and associated minerals have also reported from Paleozoic ophiolitic chromitites of Central Asian Orogenic Belt of China and the Ray?Iz ophiolite in the Polar Urals, Russia (Yang et al., 2015a, b; Tian et al., 2015; Huang et al, 2015). Importantly, in?situ diamonds have been recovered in chromitites of both the Luobusa ophiolite in Tbet and the Ray?Iz ophiolite in Russia (Yang et al., 2014, 2015a). The extensive occurrences of such ultra?high pressure (UHP) minerals in many ophiolites suggest formation by similar geological events in different oceans and orogenic belts of different ages. Compared to diamonds from kimberlites and UHP metamorphic belts, micro?diamonds from ophiolites present a new occurrence of diamond that requires significantly different physical and chemical conditions of formation in Earth's mantle. The forms of chromite and qingsongites (BN) indicate that ophiolitic chromitite may form at depths of >150?380 km or even deeper in the mantle (Yang et al., 2007; Dobrthinetskaya et al., 2009). The very light C isotope composition (?13C ?18 to ?28) of these ophiolitic diamonds and their Mn?bearing mineral inclusions, as well as coesite and clinopyroxene lamallae in chromite grains all indicate recycling of ancient continental or oceanic crustal materials into the deep mantle (>300 km) or down to the mantle transition zone via subduction (Yang et al., 2014, 2015a; Robinson et al., 2015; Moe et al., 2018). These new observations and new data strongly suggest that micro?diamonds and their host podiform chromitite may have formed near the transition zone in the deep mantle, and that they were then transported upward into shallow mantle depths by convection processes. The in?situ occurrence of micro?diamonds has been well?demonstrated by different groups of international researchers, along with other UHP minerals in podiform chromitites and ophiolitic peridotites clearly indicate their deep mantle origin and effectively address questions of possible contamination during sample processing and analytical work. The widespread occurrence of ophiolite?hosted diamonds and associated UHP mineral groups suggests that they may be a common feature of in?situ oceanic mantle. The fundamental scientific question to address here is how and where these micro?diamonds and UHP minerals first crystallized, how they were incorporated into ophiolitic chromitites and peridotites and how they were preserved during transport to the surface. Thus, diamonds and UHP minerals in ophiolites have raised new scientific problems and opened a new window for geologists to study recycling from crust to deep mantle and back to the surface.
Abstract: Farrι?de?Pablo et al. (2018) report a new occurrence of in situ microdiamonds enclosed in chromite from ophiolitic chromitite pods hosted in the Tehuitzingo serpentinite of southern Mexico. The discovery enlarges the number of occurrence of the ophiolite?hosted microdiamonds to 7 countries in the world, including India (Das, 2015, 2017), Albania (Xiong et al., 2017; Wu et al., 2017), Turkey (Lian et al., 2017), Myanmar (Chen et al., 2018), Russia (Yang et al., 2015), and China (Bai et al., 1993; Xu et al., 2009). The microdiamonds occur in ophiolitic podiform chromitites and peridotites, and are generally interpreted as UHP phases formed at pressures > 4 GPa (Yang et al., 2014; Griffin et al., 2016; Das et al., 2017). However, Farrι?de?Pablo et al. (2018) conclude that the Tehuitzingo diamonds were formed under low?temperature and low?pressure conditions during serpentinization, which challenges the current knowledge of diamond formation. Here, we discuss several lines of evidence that do not support the authors' conclusion.
Abstract: Large peridotite massifs are scattered along the 1500?km length of the Yarlung-Zangbo Suture Zone (southern Tibet, China), the major suture between Asia and Greater India. Diamonds occur in the peridotites and chromitites of several massifs, together with an extensive suite of trace phases that indicate extremely low fO2 (SiC, nitrides, carbides, native elements) and/or ultrahigh pressures (UHP) (diamond, TiO2 II, coesite, possible stishovite). New physical and isotopic (C, N) studies of the diamonds indicate that they are natural, crystallized in a disequilibrium, high-T environment, and spent only a short time at mantle temperatures before exhumation and cooling. These constraints are difficult to reconcile with previous models for the history of the diamond-bearing rocks. Possible evidence for metamorphism in or near the upper part of the Transition Zone includes the following: (1) chromite (in disseminated, nodular and massive chromitites) containing exsolved pyroxenes and coesite, suggesting inversion from a high-P polymorph of chromite; (2) microstructural studies suggesting that the chromitites recrystallized from fine-grained, highly deformed mixtures of wadsleyite and an octahedral polymorph of chromite; (3) a new cubic Mg-silicate, with the space group of ringwoodite but an inverse-spinel structure (all Si in octahedral coordination); (4) harzburgites with coarsely vermicular symplectites of opx + Cr-Al spinel ± cpx; reconstructions suggest that these are the breakdown products of majoritic garnets, with estimated minimum pressures to?>?13?GPa. Evidence for a shallow pre-metamorphic origin for the chromitites and peridotites includes the following: (1) trace-element data showing that the chromitites are typical of suprasubduction-zone (SSZ) chromitites formed by magma mixing or mingling, consistent with Hf-isotope data from magmatic (375?Ma) zircons in the chromitites; (2) the composition of the new cubic Mg-silicate, which suggests a low-P origin as antigorite, subsequently dehydrated; (3) the peridotites themselves, which carry the trace element signature of metasomatism in an SSZ environment, a signature that must have been imposed before the incorporation of the UHP and low-fO2 phases. A proposed P-T-t path involves the original formation of chromitites in mantle-wedge harzburgites, subduction of these harzburgites at c. 375?Ma, residence in the upper Transition Zone for >200 Myr, and rapid exhumation at c. 170-150?Ma or 130-120?Ma. Os-isotope data suggest that the subducted mantle consisted of previously depleted subcontinental lithosphere, dragged down by a subducting oceanic slab. Thermomechanical modeling shows that roll-back of a (much later) subducting slab would produce a high-velocity channelized upwelling that could exhume the buoyant harzburgites (and their chromitites) from the Transition Zone in?
Abstract: Widespread Miocene (24-8 Ma) ultrapotassic rocks and their entrained xenoliths provide information on the composition, structure, and thermal state of the sub-continental lithospheric mantle in southern Tibet during the India-Asia continental collision. The ultrapotassic rocks along the Lhasa block delineate two distinct lithospheric domains with different histories of depletion and enrichment. The eastern ultrapotassic rocks (89°E-92°E) reveal a depleted, young, and fertile lithospheric mantle (87Sr/86Srt = 0.704-0.707 [t is eruption time]; Hf depleted-mantle model age [TDM] = 377-653 Ma). The western ultrapotassic rocks (79°E-89°E) and their peridotite xenoliths (81°E) reflect a refractory harzburgitic mantle refertilized by ancient metasomatism (lavas: 87Sr/86Srt = 0.714-0.734; peridotites: 87Sr/86Srt = 0.709-0.716). These data integrated with seismic tomography suggest that upwelling asthenosphere was diverted away from the deep continental root beneath the western Lhasa block, but rose to shallower depths beneath a thinner lithosphere in the eastern part. Heating of the lithospheric mantle by the rising asthenosphere ultimately generated the ultrapotassic rocks with regionally distinct geochemical signatures reflecting the different nature of the lithospheric mantle.
Abstract: Detailed petrography, microstructure, and geochemistry of garnet pyroxenite xenoliths in Holocene basanite tuffs from maars at Lakes Bullenmerri and Gnotuk (western Victoria, southeastern Australia) have been used to track their igneous and metamorphic history, enabling the reconstruction of the thermal-tectonic evolution of the lithospheric mantle. The exsolution of orthopyroxene and garnet and rare spinel, plagioclase, and ilmenite from complex clinopyroxene megacrysts suggests that the xenoliths originally were clinopyroxene-dominant cumulates associated with minor garnet, orthopyroxene, or spinel. The compositions of exsolved phases and their host clinopyroxene were reintegrated using measured modal proportions to show that the primary clinopyroxene was enriched in Al2O3 (5.53-13.63 wt%) and crystallized at ~1300-1500 °C and 16-30 kbar. These cumulates then underwent extensive exsolution, recrystallization, and reaction during cooling, and finally equilibrated at ~950-1100 °C and 12-18 kbar before entrainment in the basanites. Rare earth element (REE) thermobarometry of garnets and coexisting clinopyroxenes preserves evidence of an intermediate stage (1032 °C and 21 kbar). These results imply that the protoliths of the garnet pyroxenite formed at a range of depths from ~50 to 100 km, and then during or shortly after cooling, they were tectonically emplaced to higher levels (~40-60 km; i.e., uplifted by at least 10-20 km) along the prevailing geotherm. This uplift may have been connected with lithosphere-scale faulting during the Paleozoic orogeny, or during Mesozoic-Cenozoic rifting of eastern Australia.
Geological Society of London, Chapter 2, pp. 27-48.
Australia, Victoria
xenoliths
Abstract: Detailed petrography, microstructure, and geochemistry of garnet pyroxenite xenoliths in Holocene basanite tuffs from maars at Lakes Bullenmerri and Gnotuk (western Victoria, southeastern Australia) have been used to track their igneous and metamorphic history, enabling the reconstruction of the thermal-tectonic evolution of the lithospheric mantle. The exsolution of orthopyroxene and garnet and rare spinel, plagioclase, and ilmenite from complex clinopyroxene megacrysts suggests that the xenoliths originally were clinopyroxene-dominant cumulates associated with minor garnet, orthopyroxene, or spinel. The compositions of exsolved phases and their host clinopyroxene were reintegrated using measured modal proportions to show that the primary clinopyroxene was enriched in Al2O3 (5.5313.63 wt%) and crystallized at ~13001500 °C and 1630 kbar. These cumulates then underwent extensive exsolution, recrystallization, and reaction during cooling, and finally equilibrated at ~9501100 °C and 1218 kba
Abstract: Moissanite (SiC) occurs in mantle and mantle-generated rocks from different tectonic settings. SiC is stable only at low oxygen fugacity (O2) ?IW. Israeli SiC is assiociated with corundum, Fe globules, native V and other phases in Cretaceous pyroclastic rocks from Mt Carmel and associated alluvial deposits[1]. The SiC grains contain inclusions of Si metal, FeSi2, FeTiSi2, FeAlSi2 and CaSi2+xSi2-x, which were liquids before being trapped during SiC crystallization. SiC has been found included in corundum, associated with Fe-Ti silicides, connecting the formation of SiC, reduced melts in corundum and conrundum itself. All grains are of the 6H polytype. ?13C ranges from - 32.1 to -24.5 and ?30Si from -0.68 to +1.42. These SiC grains are one product of the interaction of basaltic magma and mantle methane in a volcanic plumbing system. SiC crystallized from metallic melts that became immiscible during the reduction of the magma. Its low ?13C may reflect Rayleigh fractionation under reduced conditions; the variation in Si isotopes may reflect fractionation between SiC and immiscible metallic melts. SiC samples from the Udachnaya and Mir kimberlite pipes contain inclusions of Si metal, FeSi2, FeSi, FeTiSi2, Si(N,O). The SiC has ?13C ranging from -28.5 to -24.8, and ?30Si from -1.72 to +1.42. SiC from harzburgites, chromitites and pyroxenites of the Tibetan Zedang ophiolites have inclusions of Si metal and unmixed Fe-Ni-Ti-Si alloy. Their ?13C ranges from -30.6 to -24.7 and ?30Si from -0.85 to +1.26. SiC samples from these different settings show very similar characteristics, implying that they may be formed in similar mantle conditions, where the flux of mantle methane gradually reduces magmas and interacts with them to produce different reduced phases at different stages.
European Journal of Mineralogy, Vol. 29, 4, pp. 557-570.
Europe, Israel
mineralogy
Abstract: Ultrahigh-pressure (UHP) materials (e.g., diamond, high-pressure polymorph of chromite) and super-reduced (SuR) phases (e.g., carbides, nitrides, silicides and native metals) have been identified in chromitites and peridotites of the Tibetan and Polar-Urals ophiolites. These unusual assemblages suggest previously unrecognized fluid- or melt-related processes in the Earths mantle. However, the origin of the SuR phases, and in particular their relationships with the UHP materials in the ophiolites, are still enigmatic. Studies of a recently recognized SuR mineral system from Cretaceous volcanics on Mt Carmel, Israel, suggest an alternative genesis for the ophiolitic SuR phases. The Mt Carmel SuR mineral system (associated with Ti-rich corundum xenocrysts) appears to reflect the local interaction of mantle-derived CH4 ± H2 fluids with basaltic magmas in the shallow lithosphere (depths of ?30-100 km). These interactions produced desilication of the magma, supersaturation in Al2O3 leading to rapid growth of corundum, and phase assemblages requiring local oxygen fugacity (fO2) gradually dropping to ?11 log units below the iron-wόstite (IW) buffer. The strong similarities between this system and the SuR phases and associated Ti-rich corundum in the Tibetan and Polar-Urals ophiolites suggest that the ophiolitic SuR suite probably formed by local influx of CH4 ± H2 fluids within previously subducted peridotites (and included chromitites) during their rapid exhumation from the deep upper mantle to lithospheric levels. In the final stages of their ascent, the recycled peridotites and chromitites were overprinted by a shallow magmatic system similar to that observed at Mt Carmel, producing most of the SuR phases and eventually preserving them within the Tibetan and Polar-Urals ophiolites.
Abstract: Pyroxenites provide important information on mantle heterogeneity and can be used to trace mantle evolution. New major and trace element and Sr-, Nd-, and Hf-isotope analyses of minerals and whole-rock samples of garnet websterites entrained in basanite tuffs in Bullenmerri and Gnotuk maars, southeastern Australia, are here combined with detailed petrographic observations to constrain the sources and genesis of the pyroxenites, and to trace the dynamic evolution of the lithospheric mantle. Most garnet websterites have high MgO and Cr2O3 contents, relatively flat light rare earth element (LREE) patterns ([La/Nd]CN?=?077-222) and ocean island basalt-like Sr-, Nd-, and Hf-isotope compositions [87Sr/86Sr?=?070412-070657; ?Nd(t)?=?-032 to +446; ?Hf(t)=+169 to +186] in clinopyroxenes. Some samples show subduction-related signatures with strong enrichments in large ion lithophile elements and LREE, and negative anomalies in high field strength elements, as well as high 87Sr/86Sr (up to 0709), and decoupled Hf- and Nd-isotope compositions [?Nd(t)?=?-328; ?Hf(t) =?+116). These data suggest that the garnet pyroxenites represent early crystallization products of mafic melts derived from a convective mantle wedge. Hf model ages and Sm-Nd mineral isochrons suggest that these pyroxenites record at least two stages of evolution. The initial formation stage corresponds to the Paleozoic subduction of the proto-Pacific plate beneath southeastern Australia, which generated hydrous tholeiitic melts that crystallized clinopyroxene-dominated pyroxenites at ?1420-1450°C and ?75?km depth in the mantle wedge. The second stage corresponds to Eocene (c. 40?Ma) back-arc lithospheric extension, which led to uplift of the former mantle-wedge domain to 40-60?km depths, and subsequent cooling to the ambient geotherm (?950-1100°C). Extensive exsolution and recrystallization of garnet and orthopyroxene (±?ilmenite) from clinopyroxene megacrysts accompanied this stage. The timing of these mantle events coincides with vertical tectonism in the overlying crust.
Earth and Planetary Science Letters, Vol. 544, 116365 14p. Pdf
Australia
carbonatite
Abstract: Petrological and geochemical studies have revealed the contribution of garnet pyroxenites in basalt petrogenesis. However, whether primary mantle melts are produced with such signature or acquired it subsequently remains somewhat controversial. We here integrate new major-, trace-element and Sr-Nd-Hf isotopic compositions of garnet pyroxenite xenoliths in Holocene alkali basalts from Lakes Bullenmerri and Gnotuk, Southeastern Australia, to relate their petrogenesis to mantle-wedge melt circulation and subsequent lithospheric evolution. Results show that the clinopyroxenites have lower MgO and Cr2O3 contents than the associated websterites, and range in compositions from depleted LREE patterns and highly radiogenic Nd and Hf isotopic signatures in relatively low-MgO samples (Type 1), to enriched REE patterns with negative HFSE anomalies, unradiogenic Nd and Hf isotopes, and extremely radiogenic Sr-isotopic ratios in samples with higher MgO (Type 2). Such compositional variabilities suggest that these pyroxenites represent segregates from melts derived from a recycled oceanic lithosphere with a potential contribution from pelagic sediments. Variable LREE contents and isotopic compositions between those of Type 1 and 2 clinopyroxenites are observed in amphibole-bearing samples (Type 3), which are interpreted as Type 1-like protoliths metasomatized by the basaltic and carbonatitic melts, possibly parental to Type 2 clinopyroxenites. The lithosphere beneath Southeastern Australia thus has received variable melt contributions from a heterogeneous mantle-wedge source, which notably includes a subducted oceanic slab package that has retained its integrity during subduction. On this basis, we suggest that the compositional heterogeneity and temporal evolution of the subsequent Southeastern Australian basaltic magmatism were probably affected by the presence of pyroxenite fragments in the basalt source and formed by the tectonic reactivation of this lithosphere during Cenozoic rifting. This interpretation is notably consistent with a trend of Nd-Pb isotopes towards EMII in Older Volcanic Provinces (OVP basalts) and limited Sr-Nd-Pb isotopic variations towards HIMU in the Newer Volcanic Provinces (NVP basalts, including the host lavas), which also exhibit low SiO2, high FeO and high CaO/Al2O3 commonly interpreted as due to pyroxenite contributions. Therefore, the identification of a subduction signature in these rift-related lavas attests to a "lithospheric memory" of earlier subduction episodes (as documented by the xenoliths), rather than a reflection of contemporaneous subduction tectonics.
Journal of Petrology, 10.1093/petrology/egaa079 110p. Pdf
China
xenoliths
Abstract: Transformation of refractory cratonic mantle into more fertile lithologies is the key to the fate of cratonic lithosphere. This process has been extensively studied in the eastern North China Craton (NCC) while that of its western part is still poorly constrained. A comprehensive study of newly-found pyroxenite xenoliths from the Langshan area, in the northwestern part of this craton is integrated with a regional synthesis of pyroxenite and peridotite xenoliths to constrain the petrogenesis of the pyroxenites and provide an overview of the processes involved in the modification of the deep lithosphere. The Langshan pyroxenites are of two types, high-Mg# [Mg2+/(Mg2++Fe2+)*100 = ? 90, atomic ratios] olivine-bearing websterites with high equilibration temperatures (880 ? 970 oC), and low-Mg# (70 ? 80) plagioclase-bearing websterites with low equilibration temperatures (550 ? 835 oC). The high-Mg# pyroxenites show trade-off abundances of olivine and orthopyroxene, highly depleted bulk Sr-Nd (?Nd?=?+11.41, 87Sr/86Sr = ?0.7034) and low clinopyroxene Sr isotopic ratios (mean 87Sr/86Sr = ?0.703). They are considered to reflect the reaction of mantle peridotites with silica-rich silicate melts derived from the convective mantle. Their depletion in fusible components (e.g., FeO, TiO2 and Na2O) and progressive exhaustion of incompatible elements suggest melt extraction after their formation. The low-Mg# pyroxenites display layered structures, convex-upward rare earth element patterns, moderately enriched bulk Sr-Nd isotopic ratios (?Nd = -14.20 ? -16.74, 87Sr/86Sr?=?0.7070 ? 0.7078) and variable clinopyroxene Sr-isotope ratios (87Sr/86Sr?=?0.706-0.711). They are interpreted to be crustal cumulates from hypersthene-normative melts generated by interaction between the asthenosphere and heterogeneous lithospheric mantle. Combined with studies on regional peridotite xenoliths, it is shown that the thinning and refertilization of the lithospheric mantle was accompanied by crustal rejuvenation and that such processes occurred ubiquitously in the northwestern part of the NCC. A geodynamic model is proposed for the evolution of the deep lithosphere, which includes long-term mass transfer through a mantle wedge into the deep crust from the Paleozoic to the Cenozoic, triggered by subduction of the Paleo-Asian ocean and the Late Mesozoic lithospheric extension of eastern Asia.
Abstract: Transformation of refractory cratonic mantle into more fertile lithologies is the key to the fate of cratonic lithosphere. This process has been extensively studied in the eastern North China Craton (NCC) while that of its western part is still poorly constrained. A comprehensive study of newly-found pyroxenite xenoliths from the Langshan area, in the northwestern part of this craton is integrated with a regional synthesis of pyroxenite and peridotite xenoliths to constrain the petrogenesis of the pyroxenites and provide an overview of the processes involved in the modification of the deep lithosphere. The Langshan pyroxenites are of two types, high-Mg# [Mg2+/(Mg2++Fe2+)*100 = ?90, atomic ratios] olivine-bearing websterites with high equilibration temperatures (880-970 oC), and low-Mg# (70-80) plagioclase-bearing websterites with low equilibration temperatures (550-835 oC). The high-Mg# pyroxenites show trade-off abundances of olivine and orthopyroxene, highly depleted bulk Sr-Nd (?Nd = +1141, 87Sr/86Sr = ?07034) and low clinopyroxene Sr isotopic ratios (mean 87Sr/86Sr = ?0703). They are considered to reflect the reaction of mantle peridotites with silica-rich silicate melts derived from the convective mantle. Their depletion in fusible components (e.g., FeO, TiO2 and Na2O) and progressive exhaustion of incompatible elements suggest melt extraction after their formation. The low-Mg# pyroxenites display layered structures, convex-upward rare earth element patterns, moderately enriched bulk Sr-Nd isotopic ratios (?Nd = -1420- -1674, 87Sr/86Sr = 07070-07078) and variable clinopyroxene Sr-isotope ratios (87Sr/86Sr = 0706-0711). They are interpreted to be crustal cumulates from hypersthene-normative melts generated by interaction between the asthenosphere and heterogeneous lithospheric mantle. Combined with studies on regional peridotite xenoliths, it is shown that the thinning and refertilization of the lithospheric mantle was accompanied by crustal rejuvenation and that such processes occurred ubiquitously in the northwestern part of the NCC. A geodynamic model is proposed for the evolution of the deep lithosphere, which includes long-term mass transfer through a mantle wedge into the deep crust from the Paleozoic to the Cenozoic, triggered by subduction of the Paleo-Asian Ocean and the Late Mesozoic lithospheric extension of eastern Asia.
Geochemical Perspectives Letters, Vol. 7, pp. 1-2.
Mantle
moissanite
Abstract: Ballhaus et al. (2017) use electric-discharge experiments to argue that lightning strikes could produce ultra-high pressure (UHP) and super-reduced (SuR) phases "identical to those found in 'high-pressure' ophiolites" and that thus there is "not sufficient evidence to challenge long-established models of ophiolite genesis", specifically for the UHP processing of Tibetan ophiolites. However, the authors produced no evidence for UHP phases in their experiments. There are pertinent observations, relevant to the authors assertions, in the literature regarding the relationship between the UHP and SuR assemblages in the Tibetan peridotites. Their conclusions are not consistent with this evidence.
Petrogenesis of Cretaceous adakitic and shoshonitic igneous rocks in the Luzong area, Anhui Province: implications for geodynamics and Cu-Au mineralization.
Abstract: Rare metals including Lithium (Li), Beryllium (Be), Rubidium (Rb), Cesium (Cs), Zirconium (Zr), Hafnium (Hf), Niobium (Nb), Tantalum (Ta), Tungsten (W) and Tin (Sn) are important critical mineral resources. In China, rare metal mineral deposits are spatially distributed mainly in the Altay and Southern Great Xingαn Range regions in the Central Asian orogenic belt; in the Middle Qilian, South Qinling and East Qinling mountains regions in the Qilian-Qinling-Dabie orogenic belt; in the Western Sichuan and Bailongshan-Dahongliutan regions in the Kunlun-Songpan-Garze orogenic belt, and in the Northeastern Jiangxi, Northwestern Jiangxi, and Southern Hunan regions in South China. Major ore?forming epochs include Indosinian (mostly 200-240 Ma, in particular in western China) and the Yanshanian (mostly 120-160 Ma, in particular in South China). In addition, Bayan Obo, Inner Mongolia, northeastern China, with a complex formation history, hosts the largest REE and Nb deposits in China. There are six major rare metal mineral deposit types in China: Highly fractionated granite; Pegmatite; Alkaline granite; Carbonatite and alkaline rock; Volcanic; and Hydrothermal types. Two further types, namely the Leptynite type and Breccia pipe type, have recently been discovered in China, and are represented by the Yushishan Nb-Ta- (Zr-Hf-REE) and the Weilasituo Li-Rb-Sn-W-Zn-Pb deposits. Several most important controlling factors for rare metal mineral deposits are discussed, including geochemical behaviors and sources of the rare metals, highly evolved magmatic fractionation, and structural controls such as the metamorphic core complex setting, with a revised conceptual model for the latter.
Abstract: The oxygen fugacity of the upper mantle is 3-4 orders of magnitude higher than that of the lower mantle and this has been attributed to Fe2 + disproportionating into Fe3 + plus Fe0 at pressures > 24 GPa. The upper mantle might therefore have been expected to have evolved to more oxidizing compositions through geological time, but it appears that the oxygen fugacity of the upper mantle has remained constant for the last 3.5 billion years. Thus, it indicates that the mantle has been actively buffered from the accumulation of Fe3 +, and that this is linked to oxidation of diamond to carbonate coupled with reduction of Fe3 + to Fe2 +. When subducted plates penetrate into the lower mantle, compensational upwelling transports bridgmanite into the transition zone, where it breaks down to ringwoodite and majorite, releasing the ferric iron. The system returns to equilibrium through oxidation of diamond. Early in Earth history, diamond may have been enriched at the base of the transition zone in the Magma Ocean, because it is denser than peridotite melts at depths shallower than 660 km, and it is more buoyant below. Ongoing oxidation of diamond forms carbonate, leading to relatively high carbonate concentrations in the source of ocean island basalts.
Geochronology and geochemistry of felsic xenoliths in lamprophyre dikes from the southeastern margin of the North Chin a Craton: implications for the interleaving of the Dabie Sulu orogenic crust.
International Geology Review, Vol. 57, 9-10, pp. 1305-1325.
Abstract: The North China Craton is a classic case for the destruction of an ancient craton, in that it records the loss of more than 100 km of ancient refractory lithospheric mantle during the late Mesozoic and early Cenozoic. However, the mechanisms for this lithospheric thinning remain controversial in large part due to the lack of any systematic investigations of the Mesozoic asthenospheric mantle via its derived mafic rocks, which are key to understand the thinning processes. In this paper, we present detailed zircon U-Pb geochronology, elemental geochemistry, and Sr-Nd-Hf isotopic data for lamprophyres and diabase-porphyries of the Jiaodong Peninsula, in the eastern North China Craton in order to place constraints on models for lithospheric thinning. Our results show that the lamprophyres and diabase-porphyries are derived from the convective asthenospheric mantle via different degrees of partial melting, and that this mantle source was previously modified by carbonatitic liquids. Zircon LA-ICP-MS U-Pb dating suggests an emplacement age for these rocks of 123-121 Ma, the earliest evidence for asthenospherically-derived melts in the Jiaodong Peninsula so far. This emplacement age indicates that the thickness of the lithosphere in the Jiaodong Peninsula was relatively thin at that time. Co-occurrence of the asthenospheric and lithospheric mantle-derived mafic rocks as well as high-Mg adakites record a rapid transition from lithospheric to asthenospheric mantle sources, indicating that the lithosphere beneath the Jiaodong Peninsula was rapidly detached just prior to ca. 120 Ma. Lithospheric thinning of the North China Craton may have been initiated from the Jiaodong Peninsula and Bohai Sea and then propagated towards the interior of the craton.
Abstract: Widespread Miocene (24-8 Ma) ultrapotassic rocks and their entrained xenoliths provide information on the composition, structure, and thermal state of the sub-continental lithospheric mantle in southern Tibet during the India-Asia continental collision. The ultrapotassic rocks along the Lhasa block delineate two distinct lithospheric domains with different histories of depletion and enrichment. The eastern ultrapotassic rocks (89°E-92°E) reveal a depleted, young, and fertile lithospheric mantle (87Sr/86Srt = 0.704-0.707 [t is eruption time]; Hf depleted-mantle model age [TDM] = 377-653 Ma). The western ultrapotassic rocks (79°E-89°E) and their peridotite xenoliths (81°E) reflect a refractory harzburgitic mantle refertilized by ancient metasomatism (lavas: 87Sr/86Srt = 0.714-0.734; peridotites: 87Sr/86Srt = 0.709-0.716). These data integrated with seismic tomography suggest that upwelling asthenosphere was diverted away from the deep continental root beneath the western Lhasa block, but rose to shallower depths beneath a thinner lithosphere in the eastern part. Heating of the lithospheric mantle by the rising asthenosphere ultimately generated the ultrapotassic rocks with regionally distinct geochemical signatures reflecting the different nature of the lithospheric mantle.
MDPI Minerals, Vol. 10, 41;doe.10.3390/min10010041 21p. Pdf
Mantle
metasomatism
Abstract: The generation of strongly potassic melts in the mantle requires the presence of phlogopite in the melting assemblage, while isotopic and trace element analyses of ultrapotassic rocks frequently indicate the involvement of subducted crustal lithologies in the source. However, phlogopite-free experiments that focus on melting of sedimentary rocks and subsequent hybridization with mantle rocks at pressures of 1-3 GPa have not successfully produced melts with K2O >5 wt%-6 wt%, while ultrapotassic igneous rocks reach up to 12 wt% K2O. Accordingly, a two-stage process that enriches K2O and increases K/Na in intermediary assemblages in the source prior to ultrapotassic magmatism seems likely. Here, we simulate this two-stage formation of ultrapotassic magmas using an experimental approach that involves re-melting of parts of an experimental product in a second experiment. In the first stage, reaction experiments containing layered sediment and dunite produced a modally metasomatized reaction zone at the border of a depleted peridotite. For the second-stage experiment, the metasomatized dunite was separated from the residue of the sedimentary rock and transferred to a smaller capsule, and melts were produced with 8 wt%-8.5 wt% K2O and K/Na of 6-7. This is the first time that extremely K-enriched ultrapotassic melts have been generated experimentally from sediments at low pressure applicable to a post-collisional setting.
Abstract: The Huangshui'an deposit located in East Qinling (China) is an unusual case of a Si-rich carbonatite hosting economic Mo and minor Pb and REE mineralization. The role of mantle-sourced carbonatite melts and fluids in the formation of the Mo mineralization remains poorly understood. Our integrated study based on field geology, petrography, microthermometry, and LA-ICP-MS analysis of single fluid inclusions, and noble gas isotopes of pyrite permits to reconstruct the source characteristics, the magmatic-hydrothermal evolution of the carbonatitic fluids, and their controls on Mo mineralization. Fluid inclusions hosted in calcite in the carbonatite dikes have the highest concentrations of Mo (9.9-62 ppm), Ce (820-9700 ppm), Pb (1800-19500 ppm), and Zn (570-5800 ppm) and represent the least modified hydrothermal fluid derived from the carbonatite melt. Fluid inclusions hosted in calcite (Cal) and quartz (Qz2 and Qz3) of the stage I carbonatite dikes have different metal concentrations, suggesting that they formed from two distinct end member fluids. The FIA in calcite represent fluid A evolved from carbonatite melt with relatively high-ore metal concentrations, and those in quartz characterize fluid B having a crustal signature due to metasomatic reactions with the wall rocks. The FIA in quartz (Qz1) within the altered wall rock have overlapping elemental concentrations with those of massive quartz (Qz2) and vuggy quartz (Qz3) in carbonatite. This suggests that the volumetrically significant quartz in the Huangshui'an carbonatite has been formed by the introduction of Si by fluid B. The positive correlations between Rb, B, Al, Cl, and Sr in stage II fluid inclusions in late fluorite + quartz + calcite veins indicate that this late mineralization formed from the mixing of primary hydrothermal fluid B with meteoric water. The He-Ar isotope data, in combination with available C-O-Sr-Nd-Pb isotope data, constrain the carbonatite source as an enriched mantle source modified by contributions from crustal material which was probably the fertile lower crust in the region. This distinct source facilitated the enrichment in Mo, REE, and Pb in the primary carbonatite magma. The carbonatite magmatism and Mo mineralization at 209.5-207 Ma occurred in the regional-scale extensional setting at the postcollision stage of the Qinling Orogenic Belt.
Zhang, Y., Bi, H., Yu, L., Sun, S., Qui, J., Xu, C., Wang, H., Wang, R.
Evidence for metasomatic mantle carbonatitic magma extrusion in Mesoproterozoic ore hosting dolomite rocks in the middle Kunyang rift, central Yunnan China.
Progress in Natural Science, Vol. 18, 8, pp. 965-974.
Contributions to Mineralogy and Petrology, Vol. 171, 12p.
Mantle
Carbonatite
Abstract: Carbonatites host some unique ore deposits, especially rare earth elements (REE). Hydrothermal fluids have been proposed to play a significant role in the concentration and transport of REE and other rare metals in carbonatites, but experimental constraints on fluid-melt equilibria in carbonatitic systems are sparse. Here we present an experimental study of trace element (REE, Ba, Sr, Mo and W) partitioning between hydrous fluids and carbonatitic melts, bearing on potential hydrothermal activity associated with carbonatite ore-forming systems. The experiments were performed on mixtures of synthetic carbonate melts and aqueous fluids at 700-800 °C and 100-200 MPa using rapid-quench cold-seal pressure vessels and double-capsule assemblages with diamond traps for analyzing fluid precipitates in the outer capsule. Starting mixtures were composed of Ca, Mg and Na carbonates spiked with trace elements. Small amounts of F or Cl were added to some of the mixtures to study the effects of halogens on the element distribution. The results show that REE, Ba, Sr, Mo and W all preferentially partition into carbonatite melt and have fluid-melt distribution coefficients (D f/m) below unity. The REE partitioning is slightly dependent on the major element (Ca, Mg and Na) composition of the starting mixtures, and it is influenced by temperature, pressure, and the presence of halogens. The fluid-melt D values of individual REE vary from 0.02 to 0.15 with Df/mLu being larger than Df/mLa by a factor of 1.1-2. The halogens F and Cl have strong and opposite effects on the REE partitioning. Fluid-melt D REE are about three times higher in F-bearing compositions and ten times lower in Cl-bearing compositions than in halogen-free systems. Df/mW and Df/mMo are the highest among the studied elements and vary between 0.6 and 0.7; Df/mBa is between 0.05 and 0.09, whereas Df/mSr is at about 0.01-0.02. The results imply that carbonatite-related REE deposits were probably formed by fractional crystallization of carbonatitic melts rather than from exsolved hydrothermal fluids. The same appears to be true for a carbonatite-related Mo deposit recently discovered in China.
Abstract: The Late Cretaceous (ca. 100 Ma) diamondiferous Fort ΰ 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.
Abstract: Many carbonatites are associated both spatially and temporally with large igneous provinces (LIPs), and considered to originate from a mantle plume source lacking any contribution from recycled crustal materials. Here, we report an occurrence of carbonatite enriched in rare-earth elements (REE) and associated with the Tarim LIP in northwestern China. The Tarim LIP comprises intrusive and volcanic products of mantle plume activity spanning from ~ 300 to 280 Ma. The carbonatites at Wajilitage in the northwestern part of Tarim are dominated by calcite and dolomite varieties, and contain abundant REE minerals (principally, monazite and REE-fluorcarbonates). Th-Pb age determination of monazite yielded an emplacement age of 266 ± 5.3 Ma, i.e. appreciably younger than the eruption age of flood basalts at ~ 290 Ma. The carbonatites show low initial 87Sr/86Sr (0.7037-0.7041) and high ?Nd(t) (1.2-4) values, which depart from the isotopic characteristics of plume-derived basalts and high-Mg picrites from the same area. This indicates that the Wajilitage carbonatites derived from a mantle source isotopically distinct from the one responsible for the voluminous (ultra)mafic volcanism at Tarim. The carbonatites show ?26MgDSM3 values (? 0.99 to ? 0.65) that are significantly lower than those in typical mantle-derived rocks and rift carbonatites, but close to marine sediments and orogenic carbonatites. We propose that the carbonatites in the Tarim LIP formed by decompressional melting of recycled sediments mixed with the ambient mantle peridotite. The enriched components in the Tarim plume could be accounted for by the presence of recycled sedimentary components in the subcontinental mantle.
Abstract: Minerals recovered from the deep mantle provide a rare glimpse into deep Earth processes. We report the first discovery of ferric iron-rich majoritic garnet found as inclusions in a host garnet within an eclogite xenolith originating in the deep mantle. The composition of the host garnet indicates an ultrahigh-pressure metamorphic origin, probably at a depth of ~200 km. More importantly, the ferric iron-rich majoritic garnet inclusions show a much deeper origin, at least at a depth of 380 km. The majoritic nature of the inclusions is confirmed by mineral chemistry, x-ray diffraction, and Raman spectroscopy, and their depth of origin is constrained by a new experimental calibration. The unique relationship between the majoritic inclusions and their host garnet has important implications for mantle dynamics within the deep asthenosphere. The high ferric iron content of the inclusions provides insights into the oxidation state of the deep upper mantle.
Abstract: Many carbonatites are associated both spatially and temporally with large igneous provinces (LIPs), and considered to originate from a mantle plume source lacking any contribution from recycled crustal materials. Here, we report an occurrence of carbonatite enriched in rare-earth elements (REE) and associated with the Tarim LIP in northwestern China. The Tarim LIP comprises intrusive and volcanic products of mantle plume activity spanning from ~ 300 to 280 Ma. The carbonatites at Wajilitage in the northwestern part of Tarim are dominated by calcite and dolomite varieties, and contain abundant REE minerals (principally, monazite and REE-fluorcarbonates). ThPb age determination of monazite yielded an emplacement age of 266 ± 5.3 Ma, i.e. appreciably younger than the eruption age of flood basalts at ~ 290 Ma. The carbonatites show low initial 87Sr/86Sr (0.70370.7041) and high ?Nd(t) (1.24) values, which depart from the isotopic characteristics of plume-derived basalts and high-Mg picrites from the same area. This indicates that the Wajilitage carbonatites derived from a mantle source isotopically distinct from the one responsible for the voluminous (ultra)mafic volcanism at Tarim. The carbonatites show ?26MgDSM3 values (? 0.99 to ? 0.65) that are significantly lower than those in typical mantle-derived rocks and rift carbonatites, but close to marine sediments and orogenic carbonatites. We propose that the carbonatites in the Tarim LIP formed by decompressional melting of recycled sediments mixed with the ambient mantle peridotite. The enriched components in the Tarim plume could be accounted for by the presence of recycled sedimentary components in the subcontinental mantle.
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 bastnδsite and parisite at the rim; Type 3 apatite has a linear array associated with fluorite and bastnδsite veinlets. Type 2 monazite occurs as clusters intergrowing with parisite and fluorite. Type 3 and 4 monazites occur as polymineralic (fluorite and bastnδsite) 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.
Geochimica et Cosmochimica Acta, Vol. 225, pp. 1-16.
Technology
geobarometry
Abstract: Majoritic garnet [(Ca, Mg, Fe2+)3(Fe3+, Al, Si)2(SiO4)3] is one of the predominant and important constituents of upper mantle peridotite and ultra-deep subducted slabs. Majoritic substitution in garnet depends on pressure, and it has been used to estimate the formation pressure of natural majoritic garnet. Ferric iron (Fe3+) substitution occurs in natural majoritic garnets from mantle diamonds and shocked meteorites. However, available majorite geobarometers were developed without considering the effect of Fe3+ substitution in the structure. In this study, we systematically synthesized Fe3+- bearing majoritic garnets from 6.5?GPa to 15?GPa to evaluate the effect of Fe3+ on the majorite geobarometer. The Fe3+ contents of synthetic majoritic garnets were analyzed using the "Flank method" with the electron probe microanalyzer (EPMA). The results were compared with those based on the charge balance calculations. From the known synthesis pressures and measured Fe3+ contents, we developed a new majorite geobarometer for Fe3+-bearing majoritic garnets. Our results show that the existing majorite geobarometer, which does not take into account the Fe3+ substitution, could underestimate the formation pressure of majoritic garnets, especially for samples with a high majoritic component.
Abstract: The silico?carbonatite dykes of the Huanglongpu area, Lesser Qinling, China, are unusual in that they are quartz-bearing, Mo-mineralised and enriched in the heavy rare earth elements (HREE) relative to typical carbonatites. The textures of REE minerals indicate crystallisation of monazite-(Ce), bastnδsite-(Ce), parisite-(Ce) and aeschynite-(Ce) as magmatic phases. Burbankite was also potentially an early crystallising phase. Monazite-(Ce) was subsequently altered to produce a second generation of apatite, which was in turn replaced and overgrown by britholite-(Ce), accompanied by the formation of allanite-(Ce). Bastnδsite and parisite where replaced by synchysite-(Ce) and rφntgenite-(Ce). Aeschynite-(Ce) was altered to uranopyrochlore and then pyrochlore with uraninite inclusions. The mineralogical evolution reflects the evolution from magmatic carbonatite, to more silica-rich conditions during early hydrothermal processes, to fully hydrothermal conditions accompanied by the formation of sulphate minerals. Each alteration stage resulted in the preferential leaching of the LREE and enrichment in the HREE. Mass balance considerations indicate hydrothermal fluids must have contributed HREE to the mineralisation. The evolution of the fluorcarbonate mineral assemblage requires an increase in aCa2+ and aCO32? in the metasomatic fluid (where a is activity), and breakdown of HREE-enriched calcite may have been the HREE source. Leaching in the presence of strong, LREE-selective ligands (Cl?) may account for the depletion in late stage minerals in the LREE, but cannot account for subsequent preferential HREE addition. Fluid inclusion data indicate the presence of sulphate-rich brines during alteration, and hence sulphate complexation may have been important for preferential HREE transport. Alongside HREE-enriched magmatic sources, and enrichment during magmatic processes, late stage alteration with non-LREE-selective ligands may be critical in forming HREE-enriched carbonatites.
Abstract: Subduction zones are an important way for crustal materials to enter deep parts of the Earth. Therefore, carbonatites in orogenic belt are of great significance in revealing deep carbon cycling pathways. To date, mantle-derived carbonatites have been identified in many orogenic belts, and their origin is considered to be related to subducted sediments. However, almost all orogenic carbonatites are composed of calcite, and their C isotopic compositions show typical mantle values, lacking any evidence of sedimentary origin. Here, we report decoupling of C and Sr isotopes between intimately associated dolomite and forsterite-calcite carbonatites from Caotan in the Qinling orogen, central China. The dolomite carbonatite is mainly composed of dolomite (plus minor apatite and magnetite), which has elevated ?13CPDB values (-3.1 to -3.6 ) and low 87Sr/86Sr ratios (0.7026-0.7042). The forsterite-calcite carbonatite consists of calcite (60-65 vol. %), forsterite and its replacement products (30-35 vol. %), and magnetite. The calcite shows mantle-like ?13CPDB (-6.2 to -7.2 ) but high initial 87Sr/86Sr values (0.7053-0.7076). Neodymium and Pb isotopic compositions are comparable in the two carbonatite types. The forsterite-calcite carbonatite is interpreted to have formed by metasomatic interaction of primary dolomitic melts with eclogite in thickened lower crust during collision of the North and South China cratons. The reaction resulted in decarbonation and depletion of the carbonatitic magma in 13C. Because of its initially low REE and Pb contents, the Nd-Pb isotopic signature of the primary dolomitic melt was preserved in the forsterite-calcite carbonatite. We propose that some orogenic calcite carbonatites may not be primary mantle-derived rocks and their mantle-like ?13CPDB values may be misleading.
Abstract: The genesis of Earths largest rare earth element (REE) deposit, Bayan Obo (China), has been intensely debated, in particular whether the host dolomite marble is of sedimentary or igneous origin. The protracted (Mesoproterozoic to Paleozoic) and intricate (magmatic to metasomatic) geological processes complicate geochemical interpretations. In this study, we present a comprehensive petrographic and in situ, high-spatial resolution Sr-Pb isotopic and geochemical investigation of the host dolomite from the Bayan Obo marble. Based on petrographic evidence, the dolomite marble is divided into three facies including coarse-grained (CM), fine-grained (FM), and heterogeneous marble (HM). All carbonates are ferroan dolomite with high SrO and MnO contents (>?0.15 wt.%), consistent with an igneous origin. Trace element compositions of these dolomites are highly variable both among and within individual samples, with CM dolomite displaying the strongest LREE enrichment. In situ 206Pb/204Pb and 207Pb/204Pb ratios of the dolomite are generally consistent with mantle values. However, initial 208Pb/204Pb ratios define a large range from 35.45 to 39.75, which may result from the incorporation of radiogenic Pb released from decomposition of monazite and/or bastnδsite during Early Paleozoic metasomatism. Moreover, in situ Sr isotope compositions of dolomite indicate a large range (87Sr/86Sr?=?0.70292-0.71363). CM dolomite is characterized by a relatively consistent, unradiogenic Sr isotope composition (87Sr/86Sr?=?0.70295-0.70314), which is typical for Mesoproterozoic mantle. The variation of 87Sr/86Sr ratios together with radiogenic 206Pb/204Pb signatures for dolomite within FM and HM possibly represents recrystallization during Early Paleozoic metasomatism with the contribution of radiogenic Sr and Pb from surrounding host rocks. Therefore, our in situ geochemical data support a Mesoproterozoic igneous origin for the ore-bearing dolomite marble in the Bayan Obo deposit, which subsequently underwent intensive metasomatism during the Early Paleozoic.
Geochemistry, Geophysics, Geosystems, Vol. 20, 9, pp. 4382-4389.
Mantle
water
Abstract: We investigated the stability of the Al?rich dense hydrous magnesium silicate Phase D (PhD) in a MgO?Al2O3?SiO2?H2O system between 14 and 25 GPa at 900-1,500 °C. Al?rich PhD has a very wide stability region from 900 °C and 14 GPa to at least 1,500 °C and 25 GPa, showing strong temperature stability with increasing pressure. Al?rich PhD decomposes to Phase Egg at pressure of the mantle transition zone, whereas it decomposes to ??AlOOH phase with a temperature increase at pressure of the uppermost lower mantle. X?ray diffraction and Raman spectroscopy measurements of Al?rich PhD show that the unit?cell volume is slightly larger, but the Raman spectra resemble that of Al?free PhD. The wide stability region of Al?bearing PhD would contribute an important storage site for water in the mantle transition zone, suggesting that it can deliver a certain amount of water into the lower mantle along hot subduction and even at the normal mantle geothermal P?T condition. Furthermore, the dehydration of Al?bearing PhD might be responsible for a series of observed seismic discontinuities from the transition zone to the uppermost lower mantle and even for deep earthquakes in some typical locations.
Geostandards and Geoanalltical Research, Vol. 43, 3, pp. 543-565.
China, Europe, Sweden, Asia, Mongolia, United States, Africa, Malawi, Madagascar
REE
Abstract: Bastnδsite is the end member of a large group of carbonate-fluoride minerals with the common formula (REE) CO3FCaCO3. This group is generally widespread and, despite never occurring in large quantities, represents the major economic light rare earth element (LREE) mineral in deposits related to carbonatite and alkaline intrusions. Since bastnδsite is easily altered and commonly contains inclusions of earlier?crystallised minerals, in situ analysis is considered the most suitable method to measure its U?Th?Pb and Sr?Nd isotopic compositions. Electron probe microanalysis and laser ablation (multi?collector) inductively coupled plasma?mass spectrometry of forty?six bastnδsite samples from LREE deposits in China, Pakistan, Sweden, Mongolia, USA, Malawi and Madagascar indicate that this mineral typically has high Th and LREE and moderate U and Sr contents. Analysis of an in?house bastnδsite reference material (K?9) demonstrated that precise and accurate U?Th?Pb ages could be obtained after common Pb correction. Moreover, the Th?Pb age with its high precision is preferable to the U?Pb age because most bastnδsites have relatively high Th rather than U contents. These results will have significant implications for understanding the genesis of endogenous ore deposits and formation processes related to metallogenic geochronology research.
Abstract: Carbonatite represents a major host rock for niobium (Nb) resources worldwide. Both magmatic and post-magmatic metasomatic processes are crucial for Nb mineralization in carbonatites. However, the roles of these metasomatic processes are difficult to be evaluated due to their multiple origins and complexity of the physico-chemical conditions. In this study, we present detailed mineralogical investigations of pyrochlore group minerals and chemical U-Th-Pb geochronology of uraninite within the Miaoya carbonatite complex, aiming to better characterize the role of post-magmatic metasomatic events. The Miaoya complex (ca. 420-440?Ma) hosts the second largest carbonatite-related Nb deposit in China, mainly in the form of pyrochlore group minerals, ferrocolumbite and Nb-bearing rutile. Primary pyrochlore group minerals evolved from pyrochlore to uranpyrochlore, and ultimately reaching the betafite end-member during the magmatic stage. They have then experienced an episode of metasomatic events at 235.4?±?4.1?Ma, as determined by U-Th-Pb chemical ages of secondary uraninite. Fluids activity for uranpyrochlore alteration was concomitant with the hydrothermal reworking of REE mineralization, which was probably related to tectono-thermal events that occurred during the Triassic closure of the ancient Mianlue Ocean. During this process, hydration and decomposition of uranpyrochlore were characterized by the leaching of Na, Ca and F from its structure, the incorporation of Fe, Si, Sr and Ba from the fluids, and the final in situ replacement by secondary ferrocolumbite, uraninite and Nb-bearing rutile. In addition, parts of Nb and U liberated from uranpyrochlore by metamictization were then transported over distances of several hundreds of microns in relatively reducing (Fe, Si, S, CO2)-bearing fluids under high temperature, and were ultimately re-precipitated in amorphous Fe-Si-U-Nb-bearing oxide veins and poorly crystallized Nb-Ti-Ca-Fe-rich oxides. The relatively weak fluids activity failed to efficiently promote the Nb re-enrichment.
Physics and Chemistry of Minerals, Vol. 48, 31, 10p. Pdf
Mantle
water
Abstract: We have systematically investigated the high-pressure and high-temperature stability of Al-bearing dense hydrous magnesium silicate phases (DHMSs) in natural chlorite compositions containing?~?16 wt% H2O and?~?14 wt% Al2O3 between 14 and 25 GPa at 800-1600 °C by an MA8-type multi-anvil apparatus. A chemical mixture similar to Fe-free chlorite was also investigated for comparison. Following the pressure-temperature (P-T) path of cold subduction, the phase assemblage of phase E?+?phase D is stable at 14-25 GPa. Superhydrous phase B is observed between 16 and 22 GPa coexisting with phase E?+?phase D. Following the P-T path of hot subduction, the phase assemblage of phase E?+?garnet is identified at 14-18 GPa coexisting with the melt. The phase assemblage of superhydrous phase B?+?phase D was found at 18-25 GPa, which is expected to survive at higher P-T conditions. We have confirmed that the presence of Al could enhance the stability of DHMSs. Our results indicate that, after chlorite decomposition at the shallow region of the subduction zone, the wide stability field of Al-bearing DHMSs can increase the possibility of water transportation into the deep lower mantle.
Physics and Chemistry of Minerals, Vol. 48, 10, 6p. Pdf s00269-021-Q1163-5
Mantle
bridgmanite
Abstract: Phase D is proposed to be the most important hydrous phase at the upper part of the lower mantle, and it has been shown to coexist with bridgmanite (Brg), the most abundant mineral and main host for Al2O3 in the lower mantle. The concentration of Al in Phase D could significantly increase the thermal stability field of Phase D, therefore, partitioning of Al between Brg and Phase D is of particular importance to constrain water distribution in the deep mantle. Here, we performed high P-T experiments in MgO-Al2O3-SiO2-H2O system to investigate the partitioning of Al between Brg and Phase D up to 32 GPa and 1350 °C. Our results indicated that Al distributes strongly into Phase D relative to Brg and the partition coefficient slightly decreases with increasing temperature. Al-bearing Phase D exhibits a very high thermal stability region, but it completely decomposed around 28 GPa and 1350 °C, at which point Brg coexisted with a large amount of melt. The depth?~?850 km (28 GPa) is thus proposed to be the second choke point for hydrous minerals. This may shed new lights on several important geophysical observations in subduction zones.
Abstract: Dense hydrous magnesium silicates (DHMSs) are considered important water carriers in the deep Earth. Due to the significant effect of Fe on the stability of DHMSs, Fe-bearing Phase D (PhD) deserves much attention. However, few experiments have been conducted to determine the stability of PhD in different bulk compositions. In this study, we provide experimental constraints for the stability of PhD in the AlOOH-FeOOH-Mg1.11Si1.89O6H2.22 system between 18 and 25 GPa at 1000-1600 °C, corresponding to the P-T conditions of the mantle transition zone and uppermost lower mantle. Fe3+-bearing PhD was synthesized from the FeOOH-Mg1.11Si1.89O6H2.22 binary system with two different Fe3+ contents. The resultant Al,Fe3+-bearing compositions are close to analog specimens of the fully oxidized mid-ocean ridge basalt (MORB) and pyrolite in the AlOOH-FeOOH-Mg1.11Si1.89O6H2.22 ternary system. The substitution mechanism of Fe is shown to be dependent on pressure, and Fe3+ occupies both Mg and Si sites in PhD at pressures below 21 GPa. In contrast, Fe3+ only occupies Si site at pressures exceeding 21 GPa. The presence of Fe3+ results in a slight reduction in the thermal stability field of PhD in the FeOOH-Mg1.11Si1.89O6H2.22 system in comparison to Mg-bearing, Fe-free PhD. In contrast, Al,Fe3+-bearing PhD is more stable than Mg-bearing PhD in both MORB and pyrolite compositions. In this regard, Al,Fe3+-bearing PhD could act as a long-term water reservoir during subduction processes to the deep mantle.
Abstract: Mantle-derived carbonatites provide a unique window in the understanding of mantle characteristics and dynamics, as well as insight into the assembly and breakup of supercontinents. As a petrological indicator of extensional tectonic regimes, Archean/Proterozoic carbonatites provide important constraints on the timing of the breakup of ancient supercontinents. The majority of the carbonatites reported worldwide are Phanerozoic, in part because of the difficulty in recognizing Archean/Proterozoic carbonatites, which are characterized by strong foliation and recrystallization, and share broad petrologic similarities with metamorphosed sedimentary lithologies. Here, we report the recognition of a ~1.85?Ga carbonatite in Chaihulanzi area of Chifeng in north China based on systematic geological, petrological, geochemical, and baddeleyite U-Pb geochronological results. The carbonatite occurs as dikes or sills emplaced in Archean metasedimentary rocks and underwent intense deformation. Petrological and SEM/EDS results show that calcite and dolomite are the dominant carbonate minerals along with minor and varied amounts of Mg-rich mafic minerals, including forsterite (with Fo?>?98), phlogopite, diopside, and an accessory amount of apatite, baddeleyite, spinel, monazite, and ilmenite. The relatively high silica content together with the non-arc and OIB-like trace element signatures of the carbonatite indicates a hot mantle plume as the likely magma source. The depleted Nd isotopic signatures suggest that plume upwelling might be triggered by the accumulation of recycled crust in the deep mantle. As a part of the global-scale Columbia supercontinent, the Proterozoic tectonic evolution of the North China Craton (NCC) provides important insights into the geodynamics governing amalgamation and fragmentation of the supercontinent. The Paleo-Mesoproterozoic boundary is the key point of tectonic transition from compressional to extensional settings in the NCC. The newly identified ~1.85?Ga carbonatite provides a direct link between the long-lasting supercontinental breakup and plume activity, which might be sourced from the slab graveyard, continental crustal slabs subducted into asthenosphere, beneath the supercontinent. The carbonatite provides a precise constraint of the initiation of the continental breakup at ~1.85?Ga.
Abstract: Mantle-derived carbonatites provide a unique window in the understanding of mantle characteristics and dynamics, as well as insight into the assembly and breakup of supercontinents. As a petrological indicator of extensional tectonic regimes, Precambrian carbonatites provide important constraints on the timing of the breakup of ancient supercontinents. The majority of the carbonatites reported worldwide are Phanerozoic, in part because of the difficulty in recognizing Precambrian carbonatites, which are characterized by strong foliation and recrystallization, and share broad petrologic similarities with metamorphosed sedimentary lithologies. Here we report the recognition of a ~1.85?Ga carbonatite in Chaihulanzi area of Chifeng in north China based on systematic geological, petrological, geochemical, and baddeleyite U-Pb geochronological results. The carbonatite occurs as dikes or sills emplaced in Archean metasedimentary rocks and underwent intense deformation. Petrological and SEM/EDS results show that calcite and dolomite are the dominant carbonate minerals along with minor and varied amounts of Mg-rich mafic minerals, including forsterite (with Fo?>?98), phlogopite, diopside, and an accessory amount of apatite, baddeleyite, spinel, monazite, and ilmenite. The relatively high silica content together with the non-arc and OIB-like trace element signatures of the carbonatite indicates a hot mantle plume as the likely magma source. The depleted Nd isotopic signatures suggest that plume upwelling might be triggered by the accumulation of recycled crust in the deep mantle. As a part of the global-scale Columbia supercontinent, the Proteozoic tectonic evolution of the North China Craton (NCC) provides important insights into the geodynamics governing amalgamation and fragmentation of the supercontinent. The Paleo-Mesoproterozoic boundary is the key point of tectonic transition from compressional to extensional settings in the NCC. The newly-identified ~1.85?Ga carbonatite provides a direct link between the long-lasting supercontinental breakup and plume activity, which might be sourced from the slab graveyard, continental crustal slabs subducted into asthenosphere, beneath the supercontinent. The carbonatite provides a precise constraint of the initiation of the continental breakup at ~1.85?Ga.
Abstract: Mantle-derived carbonatites provide a unique window in the understanding of mantle characteristics and dynamics, as well as insight into the assembly and breakup of supercontinents. As a petrological indicator of extensional tectonic regimes, Precambrian carbonatites provide important constraints on the timing of the breakup of ancient supercontinents. The majority of the carbonatites reported worldwide are Phanerozoic, in part because of the difficulty in recognizing Precambrian carbonatites, which are characterized by strong foliation and recrystallization, and share broad petrologic similarities with metamorphosed sedimentary lithologies. Here we report the recognition of a ~1.85?Ga carbonatite in Chaihulanzi area of Chifeng in north China based on systematic geological, petrological, geochemical, and baddeleyite U-Pb geochronological results. The carbonatite occurs as dikes or sills emplaced in Archean metasedimentary rocks and underwent intense deformation. Petrological and SEM/EDS results show that calcite and dolomite are the dominant carbonate minerals along with minor and varied amounts of Mg-rich mafic minerals, including forsterite (with Fo?>?98), phlogopite, diopside, and an accessory amount of apatite, baddeleyite, spinel, monazite, and ilmenite. The relatively high silica content together with the non-arc and OIB-like trace element signatures of the carbonatite indicates a hot mantle plume as the likely magma source. The depleted Nd isotopic signatures suggest that plume upwelling might be triggered by the accumulation of recycled crust in the deep mantle. As a part of the global-scale Columbia supercontinent, the Proteozoic tectonic evolution of the North China Craton (NCC) provides important insights into the geodynamics governing amalgamation and fragmentation of the supercontinent. The Paleo-Mesoproterozoic boundary is the key point of tectonic transition from compressional to extensional settings in the NCC. The newly-identified ~1.85?Ga carbonatite provides a direct link between the long-lasting supercontinental breakup and plume activity, which might be sourced from the slab graveyard, continental crustal slabs subducted into asthenosphere, beneath the supercontinent. The carbonatite provides a precise constraint of the initiation of the continental breakup at ~1.85?Ga.
Geochimica et Cosmochimica Acta, in press availabe 38p. Pdf
China
metasomatism
Abstract: Water is key to many geodynamical processes in the Earth's upper mantle, yet its preservation in mantle minerals is still debated. To throw some light on this problem, we here carried out an integrated study of whole-rock and mineral chemistry, and hydrogen concentrations in olivine, orthopyroxene, and clinopyroxene within 18 spinel lherzolite samples from three localities (Lianshan, Panshishan, and Tashan) in the Nanjing area, eastern China. Whole-rock and mineral compositions suggest that the studied peridotite samples interacted with melt at different melt/rock ratios following various degrees of partial melting (up to 11%). Fourier transform infrared (FTIR) measurements show that olivine is almost dry (<1 wt ppm H2O) while the cores of orthopyroxene and clinopyroxene contain 14-151 wt ppm H2O and 41-218 wt ppm H2O, respectively. Profile analyses of >70 orthopyroxene grains, which are homogeneous in major-element compositions, covering all the studied samples show hydrogen-depleted rims, indicative of hydrogen diffusional loss. This hydrogen zonation is probably caused by hydrogen chemical diffusion controlled by the mobility of trivalent cations (most likely Al3+) in response to magma degassing or partial melting of peridotite during ascent, or interactions of peridotite with melt, or a combination of these processes. By contrast, no hydrogen zonation is observed in clinopyroxene. Based upon the comparison of chemical compositions (especially Fe and AlIV contents) of clinopyroxene within our samples with those in diffusion experiments, it is inferred that the hydrogen diffusivity in clinopyroxene should be larger than that in orthopyroxene from our samples. This inference points to that clinopyroxene within the studied samples must have experienced diffusional loss of hydrogen as well, suggesting that water concentrations in the lithospheric mantle beneath the study area are probably underestimated. Furthermore, it also implies that orthopyroxene instead of clinopyroxene most likely preserves the in-situ water concentrations at depth, at least at its core. The absence of hydrogen zonation in clinopyroxene can be attributed to its fine-grained nature and fast hydrogen diffusivity. Our FTIR data also show that Lianshan and Tashan samples have water concentration ratio between clinopyroxene and orthopyroxene (RCpx/Opx) of ?2, similar to mantle xenoliths from eastern China and other localities worldwide, yet Panshishan samples have higher RCpx/Opx values (2.3-5.9). Since hydrogen loss is suggested for both pyroxenes, RCpx/Opx of ?2 thus cannot be taken as a reliable indicator of preservation of original water concentration of mantle source and equilibrium partitioning of hydrogen between pyroxene, as opposed to previous suggestions.
Wang, Q., Wyman, D.A., Xu, J., Jian, P., Zhao, Z., Li, C., Xu, W., Ma, J., He, B.
Early Cretaceous adakitic granites in the northern Dabie Complex, central China: implications for partial melting and delamination of thickened lower crust.
Geochimica et Cosmochimica Acta, Vol. 71, 10, May 15, pp. 2609-2636.
Barium isotopic composition of the mantle constrained by carbonatites.
Goldschmidt Conference, 1p. Abstract
Africa, Tanzania, east Africa, Canada, Europe, Germany, Greenland
carbonatite
Abstract: Deep mantle origin and ultra-reducing conditions in podiform chromitite: diamonds, moissanite, and other unusual minerals in podiform chromitites from the Pozanti-Karsanti ophiolite, southern Turkey
Abstract: The sequence of replacement in groundmass perovskite and spinel from SK-1 and SK-2 kimberlites (Eastern Dharwar craton, India) has been established. Two types of perovskite occur in the studied Indian kimberlites. Type 1 perovskite is found in the groundmass, crystallized directly from the kimberlite magma, it is light rare-earth elements (LREE)-rich and Fe-poor and its ?NNO calculated value is from ?3.82 to ?0.73. The second generation of perovskite (type 2 perovskite) is found replacing groundmass atoll spinel, it was formed from hydrothermal fluids, it is LREE-free and Fe-rich and has very high ?NNO value (from 1.03 to 10.52). Type 1 groundmass perovskite may be either replaced by anatase or kassite along with aeschynite-(Ce). These differences in the alteration are related to different f(CO2) and f(H2O) conditions. Furthermore, primary perovskite may be strongly altered to secondary minerals, resulting in redistribution of rare-earth elements (REE) and, potentially, U, Pb and Th. Therefore, accurate petrographic and chemical analyses are necessary in order to demonstrate that perovskite is magmatic before proceeding to sort geochronological data by using perovskite. Ti-rich hydrogarnets (12.9 wt %-26.3 wt % TiO2) were produced during spinel replacement by late hydrothermal processes. Therefore, attention must be paid to the position of Ca-Ti-garnets in the mineral sequence and their water content before using them to classify the rock based on their occurrence.
Mineralogy and Petrology, 10.1007/s00710-018-0616-5 13p.
India
ilmentite
Abstract: Indian kimberlites occur in the Bastar craton (Central India) and in the Eastern Dharwar craton (EDC) Southern India. Nearly 100 kimberlite pipes have been discovered in the Eastern Dharwar craton of southern India, and they are distributed in three distinct fields: 1) the southern Wajrakarur kimberlite field (WKF); 2) the northern Narayanpet kimberlite field (NKF); and 3) the Raichur kimberlite field (RKF) (Chalapathi Rao et al, 2013). Nine kimberlites have been selected for this study: three came from the Siddanpalli cluster of RKF (SK-1, SK-2 and SK-3); other six kimberlites came from WKF, from Chigicherla (CC-4 and CC-5), Kalyandurg (KL-3 and KL-4), Lattavaram (P-3) and Mulligripally (P-5). The kimberlite emplacement took place during the Mesoproterozoic, around 1.1 Ga (Chalapathi Rao et al., 2013). Ilmenite is one of the classic diamond indicator minerals (DIMs) and for long it has been used as a guide for kimberlite exploration. The aim of this study is to evaluate the petrogenetic information that can be provided from the textural and geochemical study of the different ilmenite generations present in the Indian kimberlites studied in this work.
Abstract: A complex mineral sequence in a kimberlite from the Banankoro Cluster (Guinea Conakry) has been interpreted as the result of magma mixing processes. The composition of the early generations of phlogopite and spinel suggest direct crystallisation of a kimberlitic magma. However, the compositional trends found in the late generations of phlogopite and spinels could suggest magma mixing. In this context, four ilmenite generations formed. The first generations (types 1 and 2) are geikielitic and are associated with spinel and phlogopite which follow the kimberlitic compositional trends. They are interpreted as produced by crystallization from the kimberlite magma. A third generation of euhedral tabular Mg-rich ilmenite (type 3) formed during the interval between two generations of serpentine. Finally, a late generation of Mn-rich ilmenite (type 4) replaces all the Ti-rich minerals and is contemporaneous with the last generation of serpophitic non-replacing serpentine. Therefore, the formation of type 3 and type 4 ilmenite took place after the crystallization of the groundmass, during late hydrothermal process. Our results suggest a detailed textural study is necessary when use Mg-rich and Mn-rich ilmenites as KIMs.
Geophysical Research Letters, Vol. 46, 1, pp. 179-188.
Mantle
subduction
Abstract: Eclogite mainly consists of pyrope?almandine?grossular garnet and sodium?rich pyroxene (omphacite) and is a key component of the Earth's upper mantle and oceanic crust. It plays an important role in the mantle convection. The lack of thermoelastic parameters of eclogitic garnets and omphacites hampers accurate modeling of eclogite density at deep?Earth pressure?temperature conditions. In this study, we obtained the thermoelastic parameters of natural eclogitic garnets and omphacites and then modeled the densities of high?Fe and low?Fe eclogites in the subducted oceanic crust and the normal upper mantle. In the upper mantle, eclogite enhances the slab subduction into the transition zone; however, the presence of the metastable low?Fe eclogite would promote the slab stagnation within the upper range of the transition zone. Additionally, eclogite can explain positive density anomalies at depths of 100-200 km of the upper mantle of Asia identified by seismic observations.
Geochimica et Cosmochimica Acta, in press available doi.org/10.1016 / j.gca.2019.06.041 36p.
Africa, Tanzania, Canada, East Africa, Europe, Germany, Greenland
deposit - Oldoinyo Lengai
Abstract: To investigate the behaviour of Ba isotopes during carbonatite petrogenesis and to explore the possibility of using carbonatites to constrain the Ba isotopic composition of the mantle, we report high-precision Ba isotopic analyses of: (1) carbonatites and associated silicate rocks from the only active carbonatite volcano, Oldoinyo Lengai, Tanzania, and (2) Archean to Cenozoic carbonatites from Canada, East Africa, Germany and Greenland. Carbonatites and associated phonolites and nephelinites from Oldoinyo Lengai have similar ?137/134Ba values that range from +0.01 to +0.03, indicating that Ba isotope fractionation during carbonatite petrogenesis is negligible. The limited variation in ?137/134Ba values from ?0.03 to +0.09 for most carbonatite samples suggests that their mantle sources have a relatively homogeneous Ba isotopic composition. Based on the carbonatites investigated in this work, the average ?137/134Ba value of their mantle sources is estimated to be +0.04?±?0.06 (2SD, n?=?16), which is similar to the average value of +0.05?±?0.06 for mid-ocean ridge basalts. The lower ?137/134Ba value of ?0.08 in a Canadian sample and higher ?137/134Ba values of +0.14 and?+?0.23 in two Greenland samples suggest local mantle isotopic heterogeneity that may reflect the incorporation of recycled crustal materials in their sources.
Abstract: To investigate the behaviour of Ba isotopes during carbonatite petrogenesis and to explore the possibility of using carbonatites to constrain the Ba isotopic composition of the mantle, we report high-precision Ba isotopic analyses of: (1) carbonatites and associated silicate rocks from the only active carbonatite volcano, Oldoinyo Lengai, Tanzania, and (2) Archean to Cenozoic carbonatites from Canada, East Africa, Germany and Greenland. Carbonatites and associated phonolites and nephelinites from Oldoinyo Lengai have similar ?137/134Ba values that range from +0.01 to +0.03, indicating that Ba isotope fractionation during carbonatite petrogenesis is negligible. The limited variation in ?137/134Ba values from ?0.03 to +0.09 for most carbonatite samples suggests that their mantle sources have a relatively homogeneous Ba isotopic composition. Based on the carbonatites investigated in this work, the average ?137/134Ba value of their mantle sources is estimated to be +0.04?±?0.06 (2SD, n?=?16), which is similar to the average value of +0.05?±?0.06 for mid-ocean ridge basalts. The lower ?137/134Ba value of ?0.08 in a Canadian sample and higher ?137/134Ba values of +0.14 and?+?0.23 in two Greenland samples suggest local mantle isotopic heterogeneity that may reflect the incorporation of recycled crustal materials in their sources.
Geochimica et Cosmochimica Acta, Vol. 278, pp. 235-243.
Mantle
carbonatite
Abstract: To investigate the behaviour of Ba isotopes during carbonatite petrogenesis and to explore the possibility of using carbonatites to constrain the Ba isotopic composition of the mantle, we report high-precision Ba isotopic analyses of: (1) carbonatites and associated silicate rocks from the only active carbonatite volcano, Oldoinyo Lengai, Tanzania, and (2) Archean to Cenozoic carbonatites from Canada, East Africa, Germany and Greenland. Carbonatites and associated phonolites and nephelinites from Oldoinyo Lengai have similar ?137/134Ba values that range from +0.01 to +0.03, indicating that Ba isotope fractionation during carbonatite petrogenesis is negligible. The limited variation in ?137/134Ba values from ?0.03 to +0.09 for most carbonatite samples suggests that their mantle sources have a relatively homogeneous Ba isotopic composition. Based on the carbonatites investigated in this work, the average ?137/134Ba value of their mantle sources is estimated to be +0.04?±?0.06 (2SD, n?=?16), which is similar to the average value of +0.05?±?0.06 for mid-ocean ridge basalts. The lower ?137/134Ba value of ?0.08 in a Canadian sample and higher ?137/134Ba values of +0.14 and?+?0.23 in two Greenland samples suggest local mantle isotopic heterogeneity that may reflect the incorporation of recycled crustal materials in their sources.
Petrogenesis of Cretaceous adakitic and shoshonitic igneous rocks in the Luzong area, Anhui Province: implications for geodynamics and Cu-Au mineralization.
Nature Communications, 10.10.1038/s4167-021-266668-z 14p. Pdf
Mantle
olivine
Abstract: Oxygen isotope ratios in mantle-derived magmas that differ from typical mantle values are generally attributed to crustal contamination, deeply subducted crustal material in the mantle source or primordial heterogeneities. Here we provide an alternative view for the origin of light oxygen-isotope signatures in mantle-derived magmas using kimberlites, carbonate-rich magmas that assimilate mantle debris during ascent. Olivine grains in kimberlites are commonly zoned between a mantle-derived core and a magmatic rim, thus constraining the compositions of both mantle wall-rocks and melt phase. Secondary ion mass spectrometry (SIMS) analyses of olivine in worldwide kimberlites show a remarkable correlation between mean oxygen-isotope compositions of cores and rims from mantle-like 18O/16O to lower crustal values. This observation indicates that kimberlites entraining low-18O/16O olivine xenocrysts are modified by assimilation of low-18O/16O sub-continental lithospheric mantle material. Interaction with geochemically-enriched domains of the sub-continental lithospheric mantle can therefore be an important source of apparently crustal signatures in mantle-derived magmas.
Science China Earth Sciences, Vol. 59, 3, pp. 573-582.
China
Craton, North China
Abstract: Present-day hot spots and Phanerozoic large igneous provinces (LIPs) and kimberlites mainly occur at the edges of the projections of Large Low Shear Wave Velocity Provinces (LLSVPs) on the earths surface. If a plate contains accurately dated LIPs or kimberlites, it is possible to obtain the absolute paleoposition of the plate from the LIP/kimberlite and paleomagnetic data. The presence of Middle Ordovician kimberlites in the North China Block provides an opportunity to determine the absolute paleoposition of the block during the Middle Ordovician. In addition to paleobiogeographical information and the results of previous work on global plate reconstruction for the Ordovician Period, we selected published paleomagnetic data for the North China Block during the Middle Ordovician and determined the most reasonable absolute paleoposition of the North China Block during the Middle Ordovician: paleolatitude of approximately 16.6°S to 19.1°S and paleolongitude of approximately 10°W. The block was located between the Siberian Plate and Gondwana, close to the Siberian Plate. During the Cambrian and Ordovician periods, the North China Block may have moved toward the Siberian Plate and away from the Australian Plate.
Proceedings of the National Academy of Sciences PNAS, Vol. 117, 31, pp. 18285-18291. pdf
Mantle
melting
Abstract: Deeply subducted carbonates likely cause low-degree melting of the upper mantle and thus play an important role in the deep carbon cycle. However, direct seismic detection of carbonate-induced partial melts in the Earths interior is hindered by our poor knowledge on the elastic properties of carbonate melts. Here we report the first experimentally determined sound velocity and density data on dolomite melt up to 5.9 GPa and 2046 K by in-situ ultrasonic and sink-float techniques, respectively, as well as first-principles molecular dynamics simulations of dolomite melt up to 16 GPa and 3000 K. Using our new elasticity data, the calculated VP/VS ratio of the deep upper mantle (?180-330 km) with a small amount of carbonate-rich melt provides a natural explanation for the elevated VP/VS ratio of the upper mantle from global seismic observations, supporting the pervasive presence of a low-degree carbonate-rich partial melt (?0.05%) that is consistent with the volatile-induced or redox-regulated initial melting in the upper mantle as argued by petrologic studies. This carbonate-rich partial melt region implies a global average carbon (C) concentration of 80-140 ppm. by weight in the deep upper mantle source region, consistent with the mantle carbon content determined from geochemical studies.
Abstract: Pre-magmatic continental extension often precedes the major magmatic expulsion of large igneous provinces (LIPs). However, the cause-and-effect relationship between pre-magmatic rifting and the extrusion of large amount of magma is controversial. It remains unclear whether magmatism arises as a consequence of passive rifting or whether it is related to active upwelling of the mantle. In addition, the relationship between the pre-magmatic stages and the final breakup, with the onset of conjugate passive margins, is ambiguous. In this study, we compiled available data from six LIPs (Central Atlantic, Karoo, Parana-Etendeka, Deccan, North Atlantic, and Afar igneous provinces) that successively occurred during the fragmentation of Pangea and found that pre-magmatic rift trends may show a high obliquity or even be orthogonal with respect to the future passive margins. We conclude that syn-magmatic rifts should not be directly correlated, both structurally and dynamically, to the ancient pre-magmatic rift phase. Furthermore, following the breakup of a supercontinent, seafloor spreading usually initiates within volcanic passive margins (VPMs) and then propagates away to create non-volcanic passive margins (NVPMs) as a consequence of the consumption and cooling of a sub-lithospheric positive thermal anomaly. Major transform faults often exist between VPMs and NVPMs, acting as a mechanical barrier to mantle melting and magmatism transportation.
Earth Science Reviews, in press available, 38p. Doi.org/1010.1016 /jearsciev.2019.103073
Global
carbon
Abstract: Although the deep recycling of carbon has been proposed to play a key role in producing intraplate magmatism, the question of how it controls or triggers mantle melting remains poorly understood. In addition, generation of incipient carbonated melts in the mantle and their subsequent reaction with the mantle are critical processes that can influence the geochemistry of intraplate basalts, but the details of such processes are also unclear. Here we present geochemical evidence for the existence of pervasive carbonate melt in the mantle source of Cenozoic continental intraplate highly alkali basalts (SiO2 < 45 wt%), which are volumetrically minor but widespread in eastern China. The primary magma compositions of these basalts cannot be explained by either partial melting of a single mantle source lithology or mixing of magmas derived from distinct mantle sources, but can be adequately explained by carbonate-fluxed melting of eclogite and subsequent reaction between silica-rich melts and peridotite that ultimately transformed the initial carbonated silica-rich melts into silica-undersaturated alkalic magmas. The source of the carbonate is in subducted eclogites associated with the Pacific plate, which stagnated in the mantle transition zone (MTZ). The spatial distribution of the alkali basalts is in accord with large-scale seismic low-velocity anomalies in the upper mantle above the MTZ. Similar scenarios in central-western Europe and eastern Australia lead us to propose that reaction between carbonated silica-rich melt and peridotite may be a pivotal mechanism for the generation of continental intraplate alkali basalts elsewhere in the world.
Earth Science Reviews, in press available 30p. Pdf
China
picrites
Abstract: Large igneous provinces on Earth result from anomalously enormous volcanic eruptions at high melt production rates. These eruptions are often linked to catastrophic events such as mass extinctions, global climate changes, or continental break-up. Decoding their petrogenesis is therefore of great importance for our comprehensive understanding of the evolution and geodynamics of our planet. The ~260 Ma Emeishan large igneous province is an important geological feature of SW China with world-class ore deposits and is also suggested to be linked with the Capitanian mass extinction. However, fundamental aspects of the genesis of Emeishan province's most primitive lavas (picrites), such as the source lithology (pyroxenite or peridotite), the origin of compositional variations of olivines and the melting temperature and pressure conditions, remain poorly constrained. Here, we compile information on melt inclusion and host olivine, and whole-rock compositions from the ELIP picrites and show that these data are consistent with decompression melting of a relatively homogeneous peridotitic mantle plume, with a potential temperature higher than 1560 °C. The compositional variability of the olivines and picrites can be explained by varying the equilibrium depth of primary magma segregation and does not require the contribution of a pyroxenite component as previously suggested. Our results favor a scenario for the origin of the Emeishan large igneous province in which the decompression melting during upwelling of a hot hydrous and oxidized mantle plume is accompanied by catastrophic lithospheric thinning. In combination with the now extensive multi-element geochemical data, our findings provide a starting point for re-evaluation of the petrogenesis models for large igneous provinces.
Geochimica et Cosmochimica Acta, in press available, 53p.
China
eclogite
Abstract: Alkaline basalts occur widely in intraplate settings and carbonate-bearing mantle sources such as carbonated peridotites are increasingly regarded to play a key role in their formation. Carbonated eclogites, most likely the products of subducted carbonate-bearing altered oceanic crust, are probable alternative ingredients in the mantle sources of many intraplate alkaline basalts, highlighting the importance of the subduction-driven deep carbon cycle. However, this widely proposed hypothesis remains enigmatic because the recognition of low-MgO primitive alkaline basalts predicted by experiments is scarce. Here we show that Cenozoic continental intraplate alkaline basalts occurring above the stagnant oceanic slab in the mantle transition zone beneath the Hannuoba region, eastern China, display geochemical features consistent with their origin as low-degree partial melts of carbonate-bearing eclogites. Their MgO contents correlate positively with CaO, Ba/Th and Ti/Eu, but negatively with Dy/Yb and ?Nd. Remarkably, the most primitive alkaline basalts are characterized by low MgO (<5.25 wt.%), low heavy rare earth elements and Sc contents, low CaO/Al2O3 (<0.41), low Ti/Eu (<3380), but Dy/Yb (>7.1) higher than those of ocean island basalts (OIBs). These features cannot be ascribed to differentiation from high-MgO alkaline basalts because significant amounts of crystallization of clinopyroxene and garnet did not occur during ascent. Differentiation also cannot account for the correlations of time-integrated Sr-Nd isotopes with MgO, Dy/Yb and Ba/Th. Instead, the linear correlations mainly reflect strong interaction between ascending primitive alkaline melts and the lithospheric mantle. The compositions of primitive alkaline basalts reflect the key control of garnet and clinopyroxene in the mantle residue (eclogites), and the Ti, Zr and Hf anomalies further indicate the critical effect of carbonates in the eclogite source. Partial melting of the carbonate-bearing eclogites likely occurred in the uppermost asthenosphere. The production of alkaline basalts with low MgO contents by partial melting of carbonate-bearing eclogite below the peridotite solidus in an intraplate setting has been overlooked and the magmas were instead often considered to be highly evolved. Recycled altered oceanic crust thus may not only cause metasomatism of the deep mantle but may also serve as a direct source of mafic melts. These results on natural rocks support the experiment-based model for subducted altered oceanic crustal material and also indicate its diverse fate in the mantle.
Abstract: We have found >10 in situ microdiamonds in thin sections of eclogites from the Dabie and Su-Lu regions of central eastern China since the first occurrence of microdiamond in eclogites from the Dabie Mountains (DMT) reported in 1992. The microdiamonds are found not only in the central part but also in the northern part of the DMT. Several free crystals have been recovered from the crushed eclogites from the central DMT. Most in situ microdiamonds are inclusions in garnets but a few larger ones are intergranular. Most of the diamondiferous eclogites in the central part of the DMT are associated with coesite. Most importantly, the observation of microdiamonds in northern Dabie lead us to question the supposition that this is a low-P metamorphic terrane. All the diamondiferous eclogites from both the north and central DMT are of continental affinity as demonstrated by their negative ?Nd values. Therefore, both the north and central eclogite belts in the DMT are considered to be from the deep subducted terrane. Five in situ microdiamonds and two free crystals are first reported in this paper. The dimensions of the in situ microdiamonds are 30-80 ?m and the free crystals are up to 400-00 ?m across. All the microdiamonds are confirmed as such by Raman spectroscopy. The results of an infrared spectroscopic investigation on two larger free crystals and two in situ microdiamonds show that all the microdiamonds from both the Dabie and Su-Lu regions are mixed types IaA and IaB diamonds and there is no indication of any synthetic microdiamonds in our samples because such synthetic microdiamonds are always rich in type Ib.
Processes and mechanism of Mesozoic lithospheric thinning in eastern North Chin a Craton: evidence from Mesozoic igneous rocks and deep seated xenoliths.
Earth Science Frontiers, Vol. 11, 4, pp. 309-318. Ingenta 1045384777
Wang, Q., Wyman, D.A., Xu, J., Jian, P., Zhao, Z., Li, C., Xu, W., Ma, J., He, B.
Early Cretaceous adakitic granites in the northern Dabie Complex, central China: implications for partial melting and delamination of thickened lower crust.
Geochimica et Cosmochimica Acta, Vol. 71, 10, May 15, pp. 2609-2636.
Abstract: Diamond, moissanite and a variety of other minerals, similar to those reported from ophiolites in Tibet and northern Russia, have recently been discovered in chromitites of the Hegenshan ophiolite of the Central Asian Orogenic Belt, north China. The chromitites are small, podiform and vein-like bodies hosted in dunite, clinopyroxene-bearing peridotite, troctolite and gabbro. All of the analysed chromite grains are relatively Al-rich, with Cr# [100Cr/(Cr+Al)] of about 47-53. Preliminary studies of mainly disseminated chromitite from ore body No. 3756 have identified more than 30 mineral species in addition to diamond and moissanite. These include oxides (mostly hematite, magnetite, rutile, anatase, cassiterite, and quartz), sulfides (pyrite, marcasite and others), silicates (magnesian olivine, enstatite, augite, diopside, uvarovite, pyrope, orthoclase, zircon, sphene, vesuvianite, chlorite and serpentine) and others (e.g., calcite, monazite, glauberite, iowaite and a range of metallic alloys). This study demonstrates that diamond, moissanite and other exotic minerals can occur in high-Al, as well as high-Cr chromites, and significantly extends the geographic and age range of known diamond-bearing ophiolites.
Destructive of the North Chin a craton: delamin ation or thermal/chemical erosion? Mineral chemistry and oxygen isotope insights from websterite xenoliths.
Abstract: In recent years we have confirmed the existence of ophiolite-hosted diamonds on Earth, which occur in mantle peridotites and podiform chromitites of many ophiolites. These diamonds differ significantly from most kimberlite varieties, particularly in their inclusions. The typical inclusions in the diamonds are Mn-rich phases, i.e., NiMnCo alloy, native Mn, MnO, galaxite, Mn olivine and Mn garnet. Ca-silicate perovskite, a typical lower mantle mineral, was identified as mineral inclusions in diamond. One occurs as a 60-nanometer, euhedral grain associated with NiMnCo alloy and graphite, while another one occurs as a 50-nanometer grain within a large inclusion containing both NiMnCo alloy and Nd-Se-Cu-S phase. By EDS the perovskite has Ca 48.3%, Si 37.7% and Mn 14.1% with oxygen. TEM diffraction data show that the inclusion has d-spacings and angles between adjacent lattice planes are consistent to the Ca-silicate perovskite with an orthorhombic structure. The only known source of such light carbon is organic material in surface sediments and the best known sources of abundant manganese are Fe-Mn-rich sediments and Mn nodules, both of which are common on the seafloor. Many parts of the modern seafloor are also covered by sediments with a continental provenance. Phases such as SiO2 and Al2O3 are not expected in mantle peridotites and must have been introduced from shallow levels. We propose that subduction of oceanic lithosphere carries C, Mn, Si, Al and REE to the transition zone or lower mantle where the material is mixed with highly reduced material, perhaps derived from greater depths. Crystallization of diamond from a C-rich fluid encapsulates the observed inclusions. The diamonds and associated minerals are incorporated into chromite grains during chromite crystallization at depth of mantle transition zone, and are carried to shallower levels by mantle convection. Accumulation of chromite grains produces podiform chromitites containing a range of exotic minerals. However, the presence of diamonds and other UHP minerals in ophiolitic peridotites indicates that such phases can persist far outside their normal stability fields.
Abstract: Various combinations of diamond, moissanite, zircon, quartz, corundum, rutile, titanite, almandine garnet, kyanite, and andalusite have been recovered from the Dangqiong peridotites. More than 80 grains of diamond have been recovered, most of which are pale yellow to reddish-orange to colorless. The grains are all 100-200 ΅m in size and mostly anhedral, but with a range of morphologies including elongated, octahedral and subhedral varieties. Their identification was confirmed by a characteristic shift in the Raman spectra between 1325 cm?1 and 1333 cm?1, mostly at 1331.51 cm?1 or 1326.96 cm?1. Integration of the mineralogical, petrological and geochemical data for the Dongqiong peridotites suggests a multi-stage formation for this body and similar ophiolites in the Yarlung-Zangbo suture zone. Chromian spinel grains and perhaps small bodies of chromitite crystallized at various depths in the upper mantle, and encapsulated the UHP, highly reduced and crustal minerals. Some oceanic crustal slabs containing the chromian spinel and their inclusion were later trapped in suprasubduction zones (SSZ), where they were modified by island arc tholeiitic and boninitic magmas, thus changing the chromian spinel compositions and depositing chromitite ores in melt channels.
Earth and Planetary Science Letters, Vol. 430, pp. 284-295.
Asia, Tibet
Luobusa Massif Type Iib
Abstract: For more than 20 years, the reported occurrence of diamonds in the chromites and peridotites of the Luobusa massif in Tibet (a complex described as an ophiolite) has been widely ignored by the diamond research community. This skepticism has persisted because the diamonds are similar in many respects to high-pressure high-temperature (HPHT) synthetic/industrial diamonds (grown from metal solvents), and the finding previously has not been independently replicated. We present a detailed examination of the Luobusa diamonds (recovered from both peridotites and chromitites), including morphology, size, color, impurity characteristics (by infrared spectroscopy), internal growth structures, trace-element patterns, and C and N isotopes. A detailed comparison with synthetic industrial diamonds shows many similarities. Cubo-octahedral morphology, yellow color due to unaggregated nitrogen (C centres only, Type Ib), metal-alloy inclusions and highly negative View the MathML source?C13 values are present in both sets of diamonds. The Tibetan diamonds (n=3n=3) show an exceptionally large range in View the MathML source?N15 (?5.6 to +28.7+28.7) within individual crystals, and inconsistent fractionation between {111} and {100} growth sectors. This in contrast to large synthetic HPHT diamonds grown by the temperature gradient method, which have with View the MathML source?N15=0 in {111} sectors and +30+30 in {100} sectors, as reported in the literature. This comparison is limited by the small sample set combined with the fact the diamonds probably grew by different processes. However, the Tibetan diamonds do have generally higher concentrations and different ratios of trace elements; most inclusions are a NiMnCo alloy, but there are also some small REE-rich phases never seen in HPHT synthetics. These characteristics indicate that the Tibetan diamonds grew in contact with a C-saturated Ni-Mn-Co-rich melt in a highly reduced environment. The stable isotopes indicate a major subduction-related contribution to the chemical environment. The unaggregated nitrogen, combined with the lack of evidence for resorption or plastic deformation, suggests a short (geologically speaking) residence in the mantle. Previously published models to explain the occurrence of the diamonds, and other phases indicative of highly reduced conditions and very high pressures, have failed to take into account the characteristics of the diamonds and the implications for their formation. For these diamonds to be seriously considered as the result of a natural growth environment requires a new understanding of mantle conditions that could produce them.
Abstract: Various combinations of diamond, moissanite, zircon, corundum, rutile and titanitehave been recovered from the Bulqiza chromitites. More than 10 grains of diamond have been recovered, most of which are pale yellow to reddishorange to colorless. The grains are all 100300 ?m in size and mostly anhedral, but with a range of morphologies including elongated, octahedral and subhedral varieties. Their identification was confirmed by a characteristic shift in the Raman spectra between 1325 cm?1 and 1333 cm?1, mostly at 1331.51 cm?1 or 1326.96 cm?1. This investigation extends the occurrence of diamond and moissanite to the Bulqiza chromitites in the Eastern Mirdita Ophiolite. Integration of the mineralogical, petrological and geochemical data of the Bulqiza chromitites suggests their multistage formation. Magnesiochromite grains and perhaps small bodies of chromitite formed at various depths in the upper mantle, and encapsulated the ultrahigh pressure, highly reduced and crustal minerals. Some oceanic crustal slabs containing the magnesiochromite and their inclusion were later trapped in suprasubduction zones, where they were modified by tholeiitic and boninitic arc magmas, thus changing the magnesiochromite compositions and depositing chromitite ores in melt channels.
Journal of Asian Earth Sciences, Vol. 159, pp. 109-129.
China, Tibet
chromitites
Abstract: The Purang harzburgite massif in SW Tibet (China) hosts abundant chrome ore deposits. Ores consist of 20 to >95% modal chromian spinel (Cr-spinel) with mylonitic fabric in imbricate shaped pods. The composition of Cr-spinel in these ores ranges from Al-rich [Cr#Sp or Cr/(Cr?+?Al)?Χ?100?=?47.60-57.56] to Cr-rich (Cr#Sp: 62.55-79.57). Bulk platinum-group element (PGE) contents of chromitites are also highly variable ranging from 17.5?ppb to ?2.5?ppm. Both metallurgical and refractory chromitites show a general enrichment in the IPGE (Os, Ir and Ru) with respect to the PPGE (Rh, Pt and Pd), resulting mostly in right-sloping primitive mantle (PM)-normalized PGE profiles. The platinum-group mineral (PGM) assemblages of both chromitite types are dominated by heterogeneously distributed, euhedral Os-bearing laurite inclusions in Cr-spinel. The Purang chromitites have quite inhomogeneous 187Os/188Os ratios (0.12289-0.13194) that are within the range of those reported for mantle-hosted chromitites from other peridotite massifs. Geochemical calculations demonstrate that the parental melts of high-Cr chromitites were boninitic, whereas those of high-Al chromitites had an arc-type tholeiitic affinity. Chromite crystallization was most likely stimulated by changes in magma compositions due to melt-peridotite interaction, leading to the establishment of a heterogeneous physicochemical environment during the early crystallization of the PGM. The highly variable PGE contents, inhomogeneous Os-isotopic compositions and varying Cr#Sp ratios of these chromitites imply a polygenetic origin for them from spatially distinct melt inputs. The generally low ?Os values (<1) of chromitites indicate that their parental melts originated within different sections of a heterogeneously depleted mantle source region. These melts were most likely produced in the mantle wedge above a downgoing lithospheric slab.
Abstract: A geometrically quantitative plate-kinematic model, based on paleomagnetism, for the initial assembly of Laurentia has taken form in the past few decades. Within this framework, there remains but one problematic interval of data predominantly from the Slave craton, which is the 1.96-1.87?Ga Coronation apparent polar wander path (APWP). The Coronation APWP shows large (?110°) back-and-forth oscillations that are difficult to explain in terms of plate motion. Nonetheless, poles from the Coronation APWP have been incorporated in various paleogeographic reconstructions of Laurentia and the supercontinent Nuna, pointing to the importance of testing its veracity. In this study, we conducted a detailed paleomagnetic and rock magnetic study of the ca. 1.87?Ga Pearson Formation, East Arm of Great Slave Lake, Northwest Territories, Canada. Our results show that Pearson Formation yields a characteristic remanent magnetization carried by single-domain or small pseudo-single-domain magnetite. The age of the magnetization is constrained to be older than Paleoproterozoic deformation and is interpreted as primary. Paleomagnetic declinations reveal a one-to-one correlation with local structural attitudes, indicating that some small blocks in the fold belt likely experienced significant (?60°) vertical-axis rotations, presumably related to large dextral displacements along the McDonald Fault system. Alternative explanations, such as true polar wander or a non-dipole magnetic field, are considered less parsimonious for the data presented here. It is suspected that some existing Christie Bay Group poles (the Stark and Tochatwi Formations), which were sampled in areas with anomalous structural attitudes and differ from time-equivalent poles obtained from areas of the Slave craton far from major transcurrent faults, may similarly suffer from vertical-axis rotation. We suggest further study before using possibly rotated Christie Bay Group poles for paleogeographic reconstructions.
Geophysical Research Letters, Vol. 46, 4, pp. 2012-2024.
South America, Colombia, Australia
craton
Abstract: Significant amounts of landmasses are brought together in a hemispheric supercontinent, then breaks up, disperse, and reform in a new supercontinent in every 400-450 Myrs. During the supercontinent cycle, global?scale continental magmatism and orogenic activity increased. The assembly and breakup of Pangaea, the latest supercontinent, are well understood today. However, the evidence becomes more sparse further back in geological history. The geological and paleomagnetic data are insufficient to determine the exact geometries of Rodinia and Columbia supercontinents. Hence, we trace the position of Cathaysia block in the Columbia supercontinent and its relationship with other continental blocks, based on its Paleoproterozoic magmatisms, metamorphisms, and sedimentations, especially ultradepleted mantle?derived rocks. This work has important implications for the mantle heterogeneity in supercontinent reconstruction.
Abstract: We report new ?13C ?values data and N?content and N?aggregation state values for microdiamonds recovered from peridotites and chromitites of the Luobusa ophiolite (Tibet) and chromitites of the Ray?Iz ophiolite in the Polar Urals (Russia). All analyzed microdiamonds contain significant nitrogen contents (from 108 up to 589 ± 20% atomic ppm) with a consistently low aggregation state, show identical IR spectra dominated by strong absorption between 1130 cm?1 and 1344 cm?1, and hence characterize Type Ib diamond. Microdiamonds from the Luobusa peridotites have ?13C ?PDB?values ranging from ?28.7 to ?16.9, and N?contents from 151 to 589 atomic ppm. The ?13C and N?content values for diamonds from the Luobusa chromitites are ?29 to ?15.5 and 152 to 428 atomic ppm, respectively. Microdiamonds from the Ray?Iz chromitites show values varying from ?27.6 to ?21.6 in ?13C and from 108 to 499 atomic ppm in N. The carbon isotopes values bear similar features with previously analyzed metamorphic diamonds from other worldwide localities, but the samples are characterized by lower N?contents. In every respect, they are different from diamonds occurring in kimberlites and impact craters. Our samples also differ from the few synthetic diamonds; we also analyzed showing enhanced ?13C ?variability and less advanced aggregation state than synthetic diamonds. Our newly obtained N?aggregation state and N?content data are consistent with diamond formation over a narrow and rather cold temperature range (i.e. <950°C), and in a short residence time (i.e. within several million years) at high temperatures in the deep mantle.
Abstract: Diamonds have been discovered in mantle peridotites and chromitites of six ophiolitic massifs along the 1300 km?long Yarlung?Zangbo suture (Bai et al., 1993; Yang et al., 2014; Xu et al., 2015), and in the Dongqiao and Dingqing mantle peridotites of the Bangong?Nujiang suture in the eastern Tethyan zone (Robinson et al., 2004; Xiong et al., 2018). Recently, in?situ diamond, coesite and other UHP mineral have also been reported in the Nidar ophiolite of the western Yarlung?Zangbo suture (Das et al., 2015, 2017). The above?mentioned diamond?bearing ophiolites represent remnants of the eastern Mesozoic Tethyan oceanic lithosphere. New publications show that diamonds also occur in chromitites in the Pozanti?Karsanti ophiolite of Turkey, and in the Mirdita ophiolite of Albania in the western Tethyan zone (Lian et al., 2017; Xiong et al., 2017; Wu et al., 2018). Similar diamonds and associated minerals have also reported from Paleozoic ophiolitic chromitites of Central Asian Orogenic Belt of China and the Ray?Iz ophiolite in the Polar Urals, Russia (Yang et al., 2015a, b; Tian et al., 2015; Huang et al, 2015). Importantly, in?situ diamonds have been recovered in chromitites of both the Luobusa ophiolite in Tbet and the Ray?Iz ophiolite in Russia (Yang et al., 2014, 2015a). The extensive occurrences of such ultra?high pressure (UHP) minerals in many ophiolites suggest formation by similar geological events in different oceans and orogenic belts of different ages. Compared to diamonds from kimberlites and UHP metamorphic belts, micro?diamonds from ophiolites present a new occurrence of diamond that requires significantly different physical and chemical conditions of formation in Earth's mantle. The forms of chromite and qingsongites (BN) indicate that ophiolitic chromitite may form at depths of >150?380 km or even deeper in the mantle (Yang et al., 2007; Dobrthinetskaya et al., 2009). The very light C isotope composition (?13C ?18 to ?28) of these ophiolitic diamonds and their Mn?bearing mineral inclusions, as well as coesite and clinopyroxene lamallae in chromite grains all indicate recycling of ancient continental or oceanic crustal materials into the deep mantle (>300 km) or down to the mantle transition zone via subduction (Yang et al., 2014, 2015a; Robinson et al., 2015; Moe et al., 2018). These new observations and new data strongly suggest that micro?diamonds and their host podiform chromitite may have formed near the transition zone in the deep mantle, and that they were then transported upward into shallow mantle depths by convection processes. The in?situ occurrence of micro?diamonds has been well?demonstrated by different groups of international researchers, along with other UHP minerals in podiform chromitites and ophiolitic peridotites clearly indicate their deep mantle origin and effectively address questions of possible contamination during sample processing and analytical work. The widespread occurrence of ophiolite?hosted diamonds and associated UHP mineral groups suggests that they may be a common feature of in?situ oceanic mantle. The fundamental scientific question to address here is how and where these micro?diamonds and UHP minerals first crystallized, how they were incorporated into ophiolitic chromitites and peridotites and how they were preserved during transport to the surface. Thus, diamonds and UHP minerals in ophiolites have raised new scientific problems and opened a new window for geologists to study recycling from crust to deep mantle and back to the surface.
International Symposium on Deep Earth Exploration and Practices, Beijing Oct. 24-26. 1 p. abstract
China
diamond genesis
Abstract: Diamonds have been discovered in mantle peridotites and chromitites of six ophiolitic massifs along the 1300 km?long Yarlung?Zangbo suture (Bai et al., 1993; Yang et al., 2014; Xu et al., 2015), and in the Dongqiao and Dingqing mantle peridotites of the Bangong?Nujiang suture in the eastern Tethyan zone (Robinson et al., 2004; Xiong et al., 2018). Recently, in?situ diamond, coesite and other UHP mineral have also been reported in the Nidar ophiolite of the western Yarlung?Zangbo suture (Das et al., 2015, 2017). The above?mentioned diamond?bearing ophiolites represent remnants of the eastern Mesozoic Tethyan oceanic lithosphere. New publications show that diamonds also occur in chromitites in the Pozanti?Karsanti ophiolite of Turkey, and in the Mirdita ophiolite of Albania in the western Tethyan zone (Lian et al., 2017; Xiong et al., 2017; Wu et al., 2018). Similar diamonds and associated minerals have also reported from Paleozoic ophiolitic chromitites of Central Asian Orogenic Belt of China and the Ray?Iz ophiolite in the Polar Urals, Russia (Yang et al., 2015a, b; Tian et al., 2015; Huang et al, 2015). Importantly, in?situ diamonds have been recovered in chromitites of both the Luobusa ophiolite in Tbet and the Ray?Iz ophiolite in Russia (Yang et al., 2014, 2015a). The extensive occurrences of such ultra?high pressure (UHP) minerals in many ophiolites suggest formation by similar geological events in different oceans and orogenic belts of different ages. Compared to diamonds from kimberlites and UHP metamorphic belts, micro?diamonds from ophiolites present a new occurrence of diamond that requires significantly different physical and chemical conditions of formation in Earth's mantle. The forms of chromite and qingsongites (BN) indicate that ophiolitic chromitite may form at depths of >150?380 km or even deeper in the mantle (Yang et al., 2007; Dobrthinetskaya et al., 2009). The very light C isotope composition (?13C ?18 to ?28) of these ophiolitic diamonds and their Mn?bearing mineral inclusions, as well as coesite and clinopyroxene lamallae in chromite grains all indicate recycling of ancient continental or oceanic crustal materials into the deep mantle (>300 km) or down to the mantle transition zone via subduction (Yang et al., 2014, 2015a; Robinson et al., 2015; Moe et al., 2018). These new observations and new data strongly suggest that micro?diamonds and their host podiform chromitite may have formed near the transition zone in the deep mantle, and that they were then transported upward into shallow mantle depths by convection processes. The in?situ occurrence of micro?diamonds has been well?demonstrated by different groups of international researchers, along with other UHP minerals in podiform chromitites and ophiolitic peridotites clearly indicate their deep mantle origin and effectively address questions of possible contamination during sample processing and analytical work. The widespread occurrence of ophiolite?hosted diamonds and associated UHP mineral groups suggests that they may be a common feature of in?situ oceanic mantle. The fundamental scientific question to address here is how and where these micro?diamonds and UHP minerals first crystallized, how they were incorporated into ophiolitic chromitites and peridotites and how they were preserved during transport to the surface. Thus, diamonds and UHP minerals in ophiolites have raised new scientific problems and opened a new window for geologists to study recycling from crust to deep mantle and back to the surface.
Abstract: Precise measurement of variations in the local gravitational acceleration is valuable for natural hazard forecasting, prospecting, and geophysical studies. Common issues of the present gravimetry technologies include their high cost, high mass, and large volume, which can potentially be solved by micro-electromechanical-system (MEMS) technology. However, the reported MEMS gravimeter does not have a high sensitivity and a large dynamic range comparable with those of the present commercial gravimeters, lowering its practicability and ruling out worldwide deployment. In this paper, we introduce a more practical MEMS gravimeter that has a higher sensitivity of 8??Gal/?Hz and a larger dynamic range of 8000 mGal by using an advanced suspension design and a customized optical displacement transducer. The proposed MEMS gravimeter has performed the co-site earth tides measurement with a commercial superconducting gravimeter GWR iGrav with the results showing a correlation coefficient of 0.91.
Yang, J.S., Wirth, R., Wiedenbeck, M., Griffin, W.L., Meng, F.C., Chen, S.Y., Bai, W.J., Xu, X.X., Makeeyev, A.B., Bryanchaniniova, N.I.
Diamonds and highly reduced minerals from chromitite of the Ray-Iz ophiolite of the Polar Urals: deep origin of podiform chromitites and ophiolitic diamonds.
Geochimica et Cosmochimica Acta, in press available, 46p.
Russia, Siberia
deposit - Obnazhennaya
Abstract: The Obnazhennaya kimberlite in the NE Siberian craton hosts a most unusual cratonic xenolith suite, with common rocks rich in pyroxenes and garnet, and no sheared peridotites. We report petrographic and chemical data for whole rocks (WR) and minerals of 20 spinel and garnet peridotites from Obnazhennaya with Re-depletion Os isotope ages of 1.8-2.9 Ga (Ionov et al., 2015a) as well as 2 pyroxenites. The garnet-bearing rocks equilibrated at 1.6-2.8 GPa and 710-1050°C. Some xenoliths contain vermicular spinel-pyroxene aggregates with REE patterns in clinopyroxene mimicking those of garnet. The peridotites show significant scatter of Mg# (0.888-0.924), Cr2O3 (0.2-1.4 wt.%) and high NiO (0.3-0.4 wt.%). None are pristine melting residues. Low-CaO-Al2O3 (?0.9 wt.%) dunites and harzburgites are melt-channel materials. Peridotites with low to moderate Al2O3 (0.4-1.8 wt.%) usually have CaO > Al2O3, and some have pockets of calcite texturally equilibrated with olivine and garnet. Such carbonates, exceptional in mantle xenoliths and reported here for the first time for the Siberian mantle, provide direct evidence for modal makeover and Ca and LREE enrichments by ephemeral carbonate-rich melts. Peridotites rich in CaO and Al2O3 (2.7-8.0 wt.%) formed by reaction with silicate melts. We infer that the mantle lithosphere beneath Obnazhennaya, initially formed in the Mesoarchean, has been profoundly modified. Pervasive inter-granular percolation of highly mobile and reactive carbonate-rich liquids may have reduced the strength of the mantle lithosphere leading the way for reworking by silicate melts. The latest events before the kimberlite eruption were the formation of the carbonate-phlogopite pockets, fine-grained pyroxenite veins and spinel-pyroxene symplectites. The reworked lithospheric sections are preserved at Obnazhennaya, but similar processes could erode lithospheric roots in the SE Siberian craton (Tok) and the North China craton, where ancient melting residues and reworked garnet-bearing peridotites are absent.The modal, chemical and Os-isotope compositions of the Obnazhennaya xenoliths produced by reaction of refractory peridotites with melts are very particular (high Ca/Al, no Mg#-Al correlations, highly variable Cr, low 187Os/188Os, continuous modal range from olivine-rich to low-olivine peridotites, wehrlites and websterites) and distinct from those of fertile lherzolites in off-craton xenoliths and peridotite massifs. These features argue against the concept of refertilization of cratonic and other refractory peridotites by mantle-derived melts as a major mechanism to form fertile to moderately depleted lherzolites in continental lithosphere. The Obnazhennaya xenoliths represent a natural rock series produced by refertilization, but include no rocks equivalent in modal, major and trace element to the fertile lherzolites. This study shows that refertilization yields broad, continuous ranges of modal and chemical compositions with common wehrlites and websterites that are rare among off-craton xenoliths.
Geochimica et Cosmochimica Acta, Vol. 224, pp. 132-153.
Russia, Siberia
deposit - Obnazhennaya
Abstract: The Obnazhennaya kimberlite in the NE Siberian craton hosts a most unusual cratonic xenolith suite, with common rocks rich in pyroxenes and garnet, and no sheared peridotites. We report petrographic and chemical data for whole rocks (WR) and minerals of 20 spinel and garnet peridotites from Obnazhennaya with Re-depletion Os isotope ages of 1.8-2.9?Ga (Ionov et al., 2015a) as well as 2 pyroxenites. The garnet-bearing rocks equilibrated at 1.6-2.8?GPa and 710-1050?°C. Some xenoliths contain vermicular spinel-pyroxene aggregates with REE patterns in clinopyroxene mimicking those of garnet. The peridotites show significant scatter of Mg# (0.888-0.924), Cr2O3 (0.2-1.4?wt.%) and high NiO (0.3-0.4?wt.%). None are pristine melting residues. Low-CaO-Al2O3 (?0.9?wt.%) dunites and harzburgites are melt-channel materials. Peridotites with low to moderate Al2O3 (0.4-1.8?wt.%) usually have CaO?>?Al2O3, and some have pockets of calcite texturally equilibrated with olivine and garnet. Such carbonates, exceptional in mantle xenoliths and reported here for the first time for the Siberian mantle, provide direct evidence for modal makeover and Ca and LREE enrichments by ephemeral carbonate-rich melts. Peridotites rich in CaO and Al2O3 (2.7-8.0?wt.%) formed by reaction with silicate melts. We infer that the mantle lithosphere beneath Obnazhennaya, initially formed in the Mesoarchean, has been profoundly modified. Pervasive inter-granular percolation of highly mobile and reactive carbonate-rich liquids may have reduced the strength of the mantle lithosphere leading the way for reworking by silicate melts. The latest events before the kimberlite eruption were the formation of the carbonate-phlogopite pockets, fine-grained pyroxenite veins and spinel-pyroxene symplectites. The reworked lithospheric sections are preserved at Obnazhennaya, but similar processes could erode lithospheric roots in the SE Siberian craton (Tok) and the North China craton, where ancient melting residues and reworked garnet-bearing peridotites are absent. The modal, chemical and Os-isotope compositions of the Obnazhennaya xenoliths produced by reaction of refractory peridotites with melts are very particular (high Ca/Al, no Mg#-Al correlations, highly variable Cr, low 187Os/188Os, continuous modal range from olivine-rich to low-olivine peridotites, wehrlites and websterites) and distinct from those of fertile lherzolites in off-craton xenoliths and peridotite massifs. These features argue against the concept of refertilization of cratonic and other refractory peridotites by mantle-derived melts as a major mechanism to form fertile to moderately depleted lherzolites in continental lithosphere. The Obnazhennaya xenoliths represent a natural rock series produced by refertilization, but include no rocks equivalent in modal, major and trace element to the fertile lherzolites. This study shows that refertilization yields broad, continuous ranges of modal and chemical compositions with common wehrlites and websterites that are rare among off-craton xenoliths.
Geochimica et Cosmochimica Acta, Vol. 267, pp. 179-195.
Africa, Tanzania
peridotite
Abstract: Hydrogen concentration profiles through olivine and pyroxene in peridotite xenoliths carried in rift basalts from northern Tanzania (Lashaine, Eledoi, and Kisite localities) show bell-shaped distributions, indicating that diffusive hydrogen loss has occurred in all minerals. Homogeneous major element concentrations and equilibration of hydrogen between the cores of olivine and coexisting pyroxene suggest that hydrogen loss resulted from diffusive degassing during host magma emplacement. For these samples, hydrogen diffusivities in olivine and coexisting pyroxene must be within the same order of magnitude, similar to experimentally determined diffusivities, but in contrast to previous observations made on xenolithic peridotites. We demonstrate here, for the first time using natural samples, that significant differences in activation energy is likely the primary parameter that causes the discrepancy between hydrogen diffusion in olivine and pyroxene observed in different suites of mantle xenoliths. Because hydrogen diffuses faster in olivine than in pyroxene as temperature increases, hydrogen loss in the Tanzanian mantle xenoliths must have occurred at relatively low temperatures (?750 - ?900 °C), whereas hydrogen loss observed in previous xenolith studies likely occurred at higher temperatures (?950 to > 1200 °C). Thus, the diffusive loss of hydrogen in the Tanzanian mantle xenoliths may have occurred at shallow depths or at the Earths surface.
Earth-Science Reviews, in press available, 70p. Pdf
China
tectonics
Abstract: Contrasting models for internal and external locations of South China within the Nuna and Rodinia supercontinents can be resolved when the current lithotectonic associations of Mesoproterozoic and older rocks units that constitute the craton are redefined into four lithotectonic domains: Kongling, Kunming-Hainan, Wuyi, and Coastal. The Kongling and Kunming-Hainan domains are characterized by isolated Archean to early Paleoproterozoic rock units and events and crop out in northern and southern South China, respectively. The Kunming-Hainan Domain is preserved in three spatially separated regions at Kunming (southwestern South China), along the Ailaoshan shear zone, and within Hainan Island. Both domains were affected by late Paleoproterozoic tectonothermal events, indicating their likely juxtaposition by this time to form the proto-Yangtze Block. Late Paleoproterozoic and Mesoproterozoic sedimentary and igneous rock units developed on the proto-Yangtze Block, especially in its southern portions, and help link the rock units that formed along the shear zone at Ailaoshan and on Hainan Island into a single, spatially unified unit prior to Paleozoic to Cenozoic structural disaggregation and translation. The Wuyi Domain consists of late Paleoproterozoic rock units within a NE-SW trending, fault-bounded block in eastern South China. The Coastal Domain lies east of the Wuyi domain and is inferred to constitute a structurally separate block. Basement to the domain is not exposed, but zircon Hf model ages from Mesozoic granites suggest Mesoproterozoic basement at depth. The Archean to Paleoproterozoic tectonothermal record of the Kongling and Kunming-Hainan domains corresponds closely with that of NW Laurentia, suggesting all were linked, probably in association with assembly and subsequent partial fragmentation of the Nuna supercontinent. Furthermore, the age and character of Mesoproterozoic magmatism and detrital zircon signature of sedimentary rocks in the proto-Yangtze Block matches well with western Laurentia and eastern Australia-Antarctica. In particular, the detrital zircon signature of late Paleoproterozoic to early Mesoproterozoic sedimentary units in the block (e.g. Dongchuan Group) share a similar age spectrum with the Wernecke Supergroup of northwest Laurentia. This, together with similarities in the type and age of Fe-Cu mineralization in the domain with that in eastern Australia-Antarctica, especially northeast Australia, suggests a location adjacent to northwest Laurentia, southern Siberia, and northeast Australia within the Nuna supercontinent. The timing and character of late Paleoproterozoic magmatic activity in the Wuyi domain along with age of detrital zircons in associated sedimentary rocks matches the record of northern India. During rifting between Australia-Antarctica and Laurentia in the late Mesoproterozoic, the proto-Yangtze Block remained linked to northeast Australia. During accretionary orogenesis in the early Neoproterozoic, the proto-Yangtze Block assembled with the Wuyi Domain along the northern margin of India. The Coastal domain likely accreted at this time forming the South China Craton. Displacement of the Hainan and Ailaoshan assemblages from southwest of the Kunming assemblage likely occurred in the Cenozoic with the activation of the Ailaoshan-Red River fault system but could have begun in the early to mid-Paleozoic based on evidence for tectonothermal events in the Hainan assemblage.
Abstract:
Water and iron are believed to be key constituents controlling the strength and density of the lithosphere and, therefore, play a crucial role in the long-term stability of cratons. On the other hand, metasomatism can modify the water and iron abundances in the mantle and possibly triggers thermo-mechanical erosion of cratonic keels. Whether local or large scale processes control water distribution in cratonic mantle remains unclear, calling for further investigation. Spinel peridotite xenoliths in alkali basalts of the Cenozoic Tok volcanic field sampled the lithospheric mantle beneath the southeastern margin of the Siberian Craton. The absence of garnet-bearing peridotite among the xenoliths, together with voluminous eruptions of basaltic magma, suggests that the craton margin, in contrast to the central part, lost its deep keel. The Tok peridotites experienced extensive and complex metasomatic reworking by evolved, Ca-Fe-rich liquids that transformed refractory harzburgite to lherzolite and wehrlite. We used polarized Fourier transform infrared spectroscopy (FTIR) to obtain water content in olivine, orthopyroxene (Opx), and clinopyroxene (Cpx) of 14 Tok xenoliths. Olivine, with a water content of 0-3 ppm H2O, was severely degassed, probably during emplacement and cooling of the host lava flow. Orthopyroxene (49-106 ppm H2O) and clinopyroxene (97-300 ppm H2O) are in equilibrium. The cores of the pyroxene grains, unlike olivine, experienced no water loss due to dehydration or addition attributable to interaction with the host magma. The water contents of Opx and Cpx are similar to those from the Kaapvaal, Tanzania, and North China cratons, but the Tok Opx has less water than previously studied Opx from the central Siberian craton (Udachnaya, 28-301 ppm; average 138 ppm). Melting models suggest that the water contents of Tok peridotites are higher than in melting residues, and argue for a post-melting (metasomatic) origin. Moreover, the water contents in Opx and Cpx of Tok peridotites are decoupled from iron enrichments or other indicators of melt metasomatism (e.g., CaO and P2O5). Such decoupling is not seen in the Udachnaya and Kaapvaal peridotites but is similar to observations on Tanzanian peridotites. Our data suggest that iron enrichments in the southeastern Siberian craton mantle preceded water enrichment. Pervasive and large-scale, iron enrichment in the lithospheric mantle may strongly increase its density and initiate a thermo-magmatic erosion. By contrast, the distribution of water in xenoliths is relatively recent and was controlled by local metasomatic processes that operate shortly before the volcanic eruption. Hence, water abundances in minerals of Tok mantle xenoliths appear to represent a snapshot of water in the vicinity of the xenolith source regions.
Geochimica et Cosmochimica Acta, Vol. 281, pp. 67-90. pdf
Russia, Siberia
deposit - Udachnaya
Abstract: Cratonic lithospheric mantle is believed to have been formed in the Archean, but kimberlite-hosted coarse peridotites from Udachnaya in the central Siberian craton typically yield Paleoproterozoic Re-depletion Os isotope ages (TRD). By comparison, olivine megacrysts from Udachnaya, sometimes called megacrystalline peridotites, often yield Archean TRD ages, but the nature of these rare materials remains enigmatic. We provide whole-rock (WR) Re-Os isotope and PGE analyses for 24 olivine-rich xenoliths from Udachnaya as well as modal and petrographic data, WR and mineral major and trace element compositions. The samples were selected based on (a) high olivine abundances in hand specimens and (b) sufficient freshness and size to yield representative WR powders. They comprise medium- to coarse-grained (olivine??1?cm) dunite, olivine megacrysts and low-orthopyroxene (11-21% opx) harzburgites equilibrated at 783-1154?°C and 3.9-6.5 GPa; coarse dunites have not been previously reported from Udachnaya; two xenoliths contain ilmenite. The harzburgites and dunites have similar WR variation ranges of Ca, Al, Fe, Cr and Mg# (0.917-0.934) typical of refractory cratonic peridotites, but the dunites tend to have higher MgO, NiO and Mg/Si. Mineral abundances and those of Ca and Al are not correlated with Mg#WR; they are not due to differences in melting degrees but are linked to metasomatism. Several samples with high 187Re/188Os show a positive linear correlation with 187Os/188Os with an apparent age of 0.37?Ga, same as eruption age of host kimberlite. Robust TRD ages were obtained for 16 xenoliths with low 187Re/188Os (0.02-0.13). TRD ages for low-opx harzburgites (1.9-2.1?Ga; average 2.0?±?0.1?Ga, 1 ?) are manifestly lower than for dunites and megacrysts (2.4-3.1?Ga); the latter define two subsets with average TRD of 2.6?±?0.1?Ga and 3.0?±?0.1?Ga, and TMA of 3.0?±?0.2?Ga and 3.3?±?0.1?Ga, respectively. Differences in olivine grain size (coarse vs. megacrystalline) are not related to age. The age relations suggest that the dunites and megacrysts could not be produced by re-melting of harzburgites, e.g. in arc settings, nor be melt channel materials in harzburgites. Instead, they are relict fragments of lithospheric mantle formed in the Archean (likely in two events at or after 2.6?Ga and 3.0?Ga) that were incorporated into cratonic lithosphere during the final assembly of the Siberian craton in the Paleoproterozoic. A multi-stage formation of the Siberian lithospheric mantle is consistent with crustal basement ages from U-Pb dating of zircons from crustal xenoliths at Udachnaya and detrital zircons from the northern Siberian craton (1.8-2.0, 2.4-2.8 and 3.0-3.4?Ga). The new data from the Siberian and other cratons suggest that the formation of strongly melt-depleted cratonic lithosphere (e.g. Mg# ?0.92) did not stop at the Archean-Proterozoic boundary as is commonly thought, but continued in the Paleoproterozoic. The same may be valid for the transition from the Archean (4-2.5?Ga) to modern tectonic regimes.
Geochimica et Cosmochimica Acta, Vol. 295, pp. 207-223.
China
nephelinites, basanites
Abstract: Widespread Cenozoic intraplate basalts from eastern China offer the opportunity to investigate the consequences of interaction between the stagnant Pacific slab and overlying asthenosphere and chemical heterogeneity within this big mantle wedge. We present and compile a comprehensive study of highly siderophile elements and Mg-Zn isotopes of this magmatic suite (60 samples including nephelinites, basanites, alkali basalts and tholeiites). The large-scale Mg-Zn isotopic anomalies documented in these basalts have been ascribed to mantle hybridization by recycled Mg-carbonates from the stagnant western Pacific plate. Our results reveal that the nephelinites and basanites are characterized by unfractionated platinum-group element (PGE) patterns normalized to primitive upper mantle (PUM) (e.g., PdN/IrN normalized to PUM?=?1.1?±?0.8, 1?), relatively high total PGE contents (e.g., Ir?=?0.25?±?0.14?ppb) and modern mantle-like 187Os/188Os (0.142?±?0.020). These characteristics are coupled with lighter Mg isotope (?26Mg?=??0.48?±?0.07) and heavier Zn isotope (?66Zn = +0.46?±?0.06) compositions compared to the mantle values (?26Mg: ?0.25?±?0.07; ?66Zn: +0.18?±?0.05). Together, these data are interpreted to reflect the oxidative breakdown of low proportions of mantle sulfides in the sources of these small-degree melts, likely caused by recycled carbonates, which then release chalcophile-siderophile elements into carbonatitic melts. By contrast, the contemporaneous alkali basalts and tholeiites are characterized by highly fractionated PGE patterns (e.g., PdN/IrN?=?4.4?±?3.3; Ir?=?0.037?±?0.027?ppb) and radiogenic 187Os/188Os (0.279?±?0.115) coupled with less fractionated Mg-Zn isotope compositions (?26Mg: ?0.39?±?0.05; ?66Zn: +0.35?±?0.03). In combination with other isotopic (e.g., Sr-Nd) and chemical (SiO2, Ce/Pb, Ba/Th, Fe/Mn) constraints, the alkali basalts and tholeiites were derived from higher degree melting of ancient pyroxenite-bearing mantle in addition to mixing with the aforementioned nephelinitic and basanitic melts. Collectively, we suggest that deep recycled carbonates promoted melting within the "big mantle wedge" leading to the generation of Cenozoic intraplate basalts across eastern China and the "redox freezing of carbonates" may cause the oxidation of Fe0 and S2-. This process may provide an important mechanism to oxidize mantle sulfides and transfer precious metals from deep mantle to crust.
Abstract: A suite of peridotite xenoliths from the Chidliak kimberlite province provides an ideal opportunity to assess the age of the mantle lithosphere beneath the eastern Hall Peninsula Block (EHPB) in southern Baffin Island, Nunavut and to provide constraints on the lithospheric architecture of this region. The new dataset comprises highly siderophile element (HSE) abundances and Re-Os isotopic compositions for 32 peridotite xenoliths sampled from four Late Jurassic-Early Cretaceous kimberlite pipes (CH-1, -6, -7, and -44). These peridotites represent strongly depleted mantle residues, with bulk-rock and olivine chemistry denoting melt extraction extents of up to 40%. The vast majority of samples show PPGE (Pt and Pd) depletion relative to IPGE (Os, Ir, and Ru) ((Pt/Ir)N: 0.10-0.96, median = 0.57; (Pd/Ir)N: 0.03-0.79, median = 0.24), coupled with mostly unradiogenic Os isotopic compositions (187Os/188Os = 0.1084-0.1170). These peridotites display strong correlations between 187Os/188Os and melt depletion indicators (such as olivine Mg number and bulk-rock Al2O3, (Pd/Ir)N), suggesting that an ancient (~2.8 Ga) melt depletion event governed the formation of the Chidliak lithosphere. The prominent mode of TRDerupt model ages at ca. 2.8 Ga matches the main crust-building ages of the EHPB, demonstrating temporal crust-mantle coupled in the Meso-Neoarchean. These ancient melt-depletion ages are present throughout the depth of the ~ 200 km thick lithospheric mantle column beneath Chidliak. The Meso-Neoarchean formation age of the EHPB mantle broadly coincides with the timing of stabilization of the lithospheric mantle beneath the Greenlandic portion of the North Atlantic Craton (NAC). This, along with the similarity in modal mineralogy, chemical composition and evolutionary history, indicates that the EHPB, southern Baffin Island was once -contiguous with the Greenlandic NAC. The mantle lithosphere beneath both the EHPB and the NAC show a similar metasomatic history, modified by multiple pulses of metasomatism. These multiple metasomatic events combined to weaken and thin the lithospheric mantle, culminating in the formation of the Labrador Sea and Davis Strait separating the EHPB from the Greenlandic NAC in the Paleocene.
Distinct mantle sources of low Ti and high Ti basalts from the western Emeishan large igneous province, SW China: implications for plume?? lithosphere interaction
Earth and Planetary Science Letters, Vol. 228, 3-4, pp. 525-546.
Abstract: EPMA data are obtained from the P-5 kimberlite from the Wajrakarur field in the Eastern Dharwar craton of southern India (EDC). The studied sample consists of xenocrysts and xenoliths set in a variable grain size groundmass of olivine (with two textures: rounded-anhedral and subhedraleuhedral), phlogopite, perovskite, spinel, pyroxene, spinel and spinel containing Ti-garnet core. Ti-rich garnet associated with spinel is a rare occurrence in kimberlites. Two types of spinel have been identified (a) fine grained (<80 ?m) and compositionally non titaniferous, and (b) large macrocrysts (>100 ?m) having replacement cores having distinctly Ti-rich (TiO2 up to 28.51 wt %) compositions. Spinel is an abundant phase varying from <20 to >300 ?m in size, mostly subhedral to euhedral in shape. Pipe-5 has atolland necklace-textured spinels in addition to the euhedral groundmass spinels. Apart from individual grains in ground mass spinel there are also spinel intergrowths with perovskite (no apparent reaction texture observed), and sieve-like intergrowths. The composition of groundmass spinel is extensively used as petrogenetic indicator mineral (Roeder and Schulze 2008). Ti-garnets contain significant Ti (21.25-28.51wt.% TiO2), Ca (15.45-27.69 wt.% CaO), Fe (2.62-24.46 wt.% FeO) and low Cr (0.08-1.52 wt.% Cr2O3) and low Al (1.40-3.87 wt.% Al2O3). Ti- garnets and their paragenetic relationships to spinel are considered here as vital petrogenetic indicators of metasomatic fluids (Dongre et al., 2016; Cheng et al., 2014), and textural association with spinel shows that Ti-garnet formed when early crystallizing spinel interacted with residual melt during magma crystallization.
Late Archean to Early Proterozoic lithospheric mantle beneath the western North Chin a craton: Sr Nd Os isotopes of peridotite xenoliths from Yangyuan and Fansi
Abstract: The continental lithosphere is not forever; some cratons have lost their original roots during the course of their evolution. Yet, it is not clear whether gravitational instability of dense lower crust is the primary driver of decratonization. This is addressed here with emphasis being placed on the North China Craton (NCC), because it represents one of the best examples of craton-root disruption in the world, and a place where models can be tested. If lower-crustal delamination was the trigger for decratonization, we would expect a clear contrast in crustal structure and composition between disturbed (rootless) and intact cratons. However, the eastern (disturbed) and western (intact) parts of the NCC show virtually identical physical structure and composition (a thin mafic lower crust and a predominantly intermediate composition overall) although the crust in the disturbed part is thinner than in the intact craton. This suggests that delamination of the lower crust was not a viable mechanism of craton-root disruption in the NCC case. Indeed, the crust beneath the NCC largely resembles those of stable Archean cratons worldwide. Therefore the delamination, if it occurred, may have taken place much earlier (Archean) than previously thought, rather than in the Mesozoic. Delamination may have been a common phenomenon in the early evolution of cratons, probably due to relatively higher mantle temperatures in the Archean Eon.
Annual Reviews of Earth and Planetary Sciences, Vol. 47, pp. 173-195.
China
craton
Abstract: The North China Craton (NCC) was originally formed by the amalgamation of the eastern and western blocks along an orogenic belt at ?1.9 Ga. After cratonization, the NCC was essentially stable until the Mesozoic, when intense felsic magmatism and related mineralization, deformation, pull-apart basins, and exhumation of the deep crust widely occurred, indicative of destruction or decratonization. Accompanying this destruction was significant removal of the cratonic keel and lithospheric transformation, whereby the thick (?200 km) and refractory Archean lithosphere mantle was replaced by a thin (<80 km) juvenile one. The decratonization of the NCC was driven by flat slab subduction, followed by a rollback of the paleo-Pacific plate during the late Mesozoic. A global synthesis indicates that cratons are mainly destroyed by oceanic subduction, although mantle plumes might also trigger lithospheric thinning through thermal erosion. Widespread crust-derived felsic magmatism and large-scale ductile deformation can be regarded as petrological and structural indicators of craton destruction.
Minerals, Vol. 10, 9, 740 10.3390/ min10090740 24p. Pdf
Russia
deposit - Muna
Abstract: The oxidation state of the mantle plays an important role in many chemical and physical processes, including magma genesis, the speciation of volatiles, metasomatism and the evolution of the Earths atmosphere. We report the first data on the redox state of the subcontinental lithospheric mantle (SCLM) beneath the Komsomolskaya-Magnitnaya kimberlite pipe (KM), Upper Muna field, central Siberian craton. The oxygen fugacity of the KM peridotites ranges from ?2.6 to 0.3 logarithmic units relative to the fayalite-magnetite-quartz buffer (?logfO2 (FMQ)) at depths of 120-220 km. The enriched KM peridotites are more oxidized (?1.0-0.3 ?logfO2 (FMQ)) than the depleted ones (from ?1.4 to ?2.6 ?logfO2 (FMQ)). The oxygen fugacity of some enriched samples may reflect equilibrium with carbonate or carbonate-bearing melts at depths >170 km. A comparison of well-studied coeval Udachnaya and KM peridotites revealed similar redox conditions in the SCLM of the Siberian craton beneath these pipes. Nevertheless, Udachnaya peridotites show wider variations in oxygen fugacity (?4.95-0.23 ?logfO2 (FMQ)). This indicates the presence of more reduced mantle domains in the Udachnaya SCLM. In turn, the established difference in the redox conditions is a good explanation for the lower amounts of resorbed diamonds in the Udachnaya pipe (12%) in comparison with the KM kimberlites (33%). The obtained results advocate a lateral heterogeneity in the oxidation state of the Siberian SCLM.
Abstract: Kimberlite-borne mantle eclogites represent an important diamond source rock. Although the origin and stability of diamond, as opposed to its low-pressure polymorph graphite, have been studied for decades, their relationship in rare natural samples where both polymorphs coexist remains poorly constrained. To shed new light on this issue, seven graphite-diamond-bearing eclogites from the kimberlite pipe Udachnaya, Siberian craton were comprehensively investigated with respect to their petrography, mineral chemical composition and omphacite 87Sr/86Sr, acquired in situ by laser ablation multicollector inductively coupled plasma mass spectrometry. The calculated P-T conditions for basaltic group eclogites (Eu/Eu* < 1) correspond to a pressure range of 48-65?GPa and temperatures of 1060-1130?°C, whereas gabbroic eclogites with positive Eu- and Sr-anomalies have a smaller pressure variation (48-58?GPa), but a larger range in temperature (990-1260?°C). Reconstructed bulk compositions for gabbroic eclogites indicate an oceanic crustal origin for their protoliths, with accumulation of plagioclase and olivine ± clinopyroxene (gabbronorite or olivine gabbro). The protoliths of basaltic eclogites probably formed from the complementary residual melt. The presence of coesite and low Mg# in basaltic eclogites suggest that their light rare earth element depletion was the result of <10?% partial melting during subsequent subduction and emplacement into the cratonic lithosphere. Extremely unradiogenic 87Sr/86Sr (070091-070186 for six of seven samples) not only provides new evidence for the Archean age (25-29?Gyr) of Yakutian graphite-diamond-bearing eclogites and for formation of their protoliths in a depleted mantle source, but also suggests that they were not significantly metasomatically overprinted after their formation, despite their extended residence in the cratonic mantle lithosphere. The mineralogical and petrographic features indicate that the primary mineral association includes garnet, omphacite, ± coesite, ± kyanite, ± rutile, graphite, and diamond. Graphite occurs in the samples in the form of idiomorphic crystals (the longest dimensions being 04-1?mm) in garnet and kyanite and extends beyond their grain boundaries. Diamonds occur as octahedral cubic transparent, slightly colored or bright yellow crystals as large as 01-2?mm. Furthermore, idiomorphic and highly ordered graphite occurs as inclusions in diamond in four samples. The carbon isotope composition for diamond and graphite has a narrow range (?4 to ?66?) for both groups (gabbroic and basaltic), indicating a mantle source and limiting the role of subducted isotopically light biogenic carbon or reduction of isotopically heavy carbonate in diamond crystallization. Importantly, the presence of graphite and diamond inclusions in garnet, omphacite, and kyanite in three samples indicates a co-formation close in time to eclogitization. Combined, the petrographic and geochemical evidence suggests that both polymorphic carbon modifications can form in the diamond stability field, as also suggested by experiments and some natural examples, although the exact mechanism remains unresolved. Furthermore, this study provides natural evidence that graphite can be preserved (metastably) deep within the diamond stability field, without recrystallizing into diamond, for a long time, ?25?Gyr.
Abstract: The mineralogical and geochemical features of titanite and associated minerals in a rare sample of kyanite-coesite-rutile-bearing eclogite from the Udachnaya-East (Vostochnaya) kimberlite pipe have been studied in detail. Subidiomorphic titanite grains (100-300 ?m) were identified in the intergranular space. The composition of individual grains of titanite is characterized by a constant presence of Al2O3, F, P2O5, Zr, and Sr impurities but varies within the xenolith. Based on the absence of titanite inclusions in the rock-forming minerals and their presence in the intergranular space, titanite was formed in the studied sample at a late stage of its formation, most likely in the process of metasomatic action of the fluid/melt. Crystallization of rock-forming minerals (garnet + omphacite + kyanite) and accessory rutile occurred jointly at 3.5 ± 0.32 GPa and 920 ± 65°?. The value of Eu/Eu* = 1.06 in the reconstructed bulk composition of the rock, the high modal content of kyanite (~17 vol %), and the value of Ca# = Ca/(Ca + Mg + Fe + Mn) > 0.5 in garnet indicate a subduction nature of the studied eclogite. Most likely, the formation of titanite in the studied sample occurred as a result of the metasomatic action of a fluid/melt enriched in calcium, strontium, large lithophilic elements, and lead, by a mechanism similar to the formation of eclogites in the units of the Western Tien Shan.
Wang, Q., Ji, S., Salisbury, M.H., Xia, B., Pan, M., Xu, Z.
Pressure dependence and anisotropy of P wave velocities in ultrahigh pressure metamorphic rocks from the Dabie Sulu orogenic belt: implications for seismic properties
Wang, Q., Shaocheng, J., Salisbury, M.H., Xia, B., Pan, M., Xu, Z.
Shear wave properties and Poisson's ratios of ultrahigh pressure metamorphic rocks from the Dabie Sulu orogenic belt, China: implications for crustal composition.
Journal of Geophysical Research, Vol. 110, B8, pp. B08411 10.1029/2004 JB003435
Journal of Asian Earth Sciences, Vol. 164, pp. 179-193.
Asia, Myanmar
peridotites
Abstract: Peridotites from the Myitkyina ophiolite are mainly composed of lherzolite and harzburgite. The lherzolites have relatively fertile compositions, with 39.40-43.40?wt% MgO, 1.90-3.17?wt% Al2O3 and 1.75-2.84?wt% CaO. They contain spinel and olivine with lower Cr# (12.6-18.2) and Fo values (88.7-91.6) than those of the harzburgites (24.5-59.7 and 89.6-91.6 respectively). The harzburgites have more refractory compositions, containing 42.40-46.23?wt% MgO, 0.50-1.64?wt% Al2O3 and 0.40-1.92?wt% CaO. PGE contents of the peridotites show an affinity to the residual mantle. Evaluation of petrological and geochemical characteristics of these peridotites suggests that the lherzolites and harzburgites represent residual mantle after low to moderate degrees of partial melting, respectively, in the spinel stability field. The U-shaped, primitive mantle-normalized REE patterns and strong positive Ta and Pb anomalies of the harzburgites suggest melt/fluid refertilization in either a MOR or SSZ setting after their formation at a MOR. Mineral separation of the peridotites has yield a range of exotic minerals, including diamond, moissanite, native Si, rutile and zircon, a collection similar to that reported for ophiolites of Tibet and the Polar Urals. The discovery of these exotic minerals in the Myitkyina ophiolite supports the view that they occur widely in the upper oceanic mantle.
Earth and Planetary Science Letters, Vol. 494, 1, pp. 92-98.
Mantle
water
Abstract: In this study, we present new experimental constraints on the phase stability and thermal equation of state of an important hydrous phase, ?-AlOOH, using synchrotron X-ray diffraction up to 142 GPa and 2500 K. Our experimental results have shown that ?-AlOOH remains stable at the whole mantle pressure-temperature conditions above the D? layer yet will decompose at the core-mantle boundary because of a dramatic increase in temperature from the silicate mantle to the metallic outer core. At the bottom transition zone and top lower mantle, the formation of ?-AlOOH by the decomposition of phase Egg is associated with a ?2.1-2.5% increase in density (?) and a ?19.7-20.4% increase in bulk sound velocity (V?). The increase in ? across the phase Egg to ?-AlOOH phase transition can facilitate the subduction of ?-AlOOH to the lower mantle. Compared to major lower-mantle phases, ?-AlOOH has the lowest ? but greatest V?, leading to an anomalous low ? /V? ratio which can help to identify the potential presence of ?-AlOOH in the region. More importantly, water released from the breakdown of ?-AlOOH at the core-mantle boundary could lower the solidus of the pyrolitic mantle to cause partial melting and/or react with Fe in the region to form the low-velocity FeO2Hx phase. The presence of partial melting and/or the accumulation of FeO2Hx phase at the CMB could be the cause for the ultra-low velocity zone. ?-AlOOH is thus an important phase to transport water to the lowermost mantle and helps to understand the origin of the ultra-low velocity zone.
Identification of UHP and non-UHP orthogneisses in the Sulu UHP terrane, eastern China: evidence from SHRIMP U-Pb dating of mineral inclusion bearing zircons.
International Geology Review, Vol. 48, 12, pp. 1067-1086.
Liu, F.L., Gerdes, A., Liou, J.G., Xue, H.M., Liang, F.H.
SHRIMP U Pb zircon dating from Sulu Dabie dolomitic marble, eastern China: constraints on prograde, ultrahigh pressure and retrograde metamorphic ages.
Journal of Metamorphic Geology, Vol. 24, 7, Sept. pp. 569-589.
Differential subduction and exhumation of crustal slices in the Sulu HP-UHP metamorphic terrane: insights from mineral inclusions, trace elements, U-Pb and Lu Hf isotope analyses of zircon in orthogneiss
Journal of Metamorphic Geology, Vol. 27, 9, pp. 805-825.
Abstract: Carbonatitic magmatism plays a significant role in Earth's carbon cycle, which is also a lithoprobe of crust-mantle interaction, mantle metasomatism and partial melting. Due to different mineral assemblages and geochemical compositions, and diverse tectonic settings, the origin of carbonatite has long been debated. At subduction zones, sediments (including carbonates) are subducted into the mantle with the downgoing oceanic slab. However, the detailed mechanism of how subducted carbonates contribute to carbonatitic magmatism remains unclear. Here we present geochronological, geochemical and isotopic study on the Taohuala Mountain carbonatite at the southern margin of the Alxa Block, North China Craton. The classification of carbonatite from the Taohuala Mountain relies strongly on the observations of obvious intrusion contact relationships and flow structures in field outcrop. The Taohuala Mountain carbonatite has SiO2 ranging from 2.37 wt.% to 11.45 wt%, high CaO (45.93-53.86 wt%) and low MgO (0.51-4.39 wt%), and is characterized by enrichment of LILE (Ba, Sr), depletion of HFSE (Nb, Ta, Zr, Hf), and slightly negative Ce and Eu anomalies. Carbonates in the samples have high 87Sr/86Sr (0.70686-0.70694) and low 143Nd/144Nd (0.511635-0.511924). Remarkably, the highly fractionated ?18OVSMOW (11.83-25.92) indicates components of both sedimentary and mantle origin. Detailed zircon in situ U-Pb dating and oxygen isotope analysis exhibit contrast ages and ?18OVSMOW from core to rim, i.e., old ages (mainly > 800 Ma), high Th/U (mainly > 0.5) and low ?18OVSMOW (6.37-11.44) in cores (inherited), whereas young ages (~ 400 Ma), low Th/U (mainly < 0.01) and high ?18OVSMOW (20.04-24.54) in rims, suggesting that the Taohuala Mountain carbonatite may have been generated from melting of subducted sedimentary carbonates. Considering all these evidences, and that the collision along Qilian Mountains was older than the carbonatite, we propose that a large volume of sedimentary carbonates subducted and remained in the lithospheric mantle under the Alxa block during the closure of the Paleo-Qilian Ocean. Subsequently, the carbonatite was formed by melting of carbonates with minor contributions from the mantle during the breakoff or rollback of the Paleo-Asian oceanic slab.
Abstract:
Carbonatitic magmatism plays a significant role in outgassing carbon from mantle and the formation of rare earth element (REE), rare metal (e.g., Nb and Th) and other types of deposits. The mechanism of REE mineralization associated with carbonatite have been widely studied. However, it is hard to understand U-Nb mineralization without Th enrichment associated with carbonatite. Here we report a carbonatite-hosted U-Nb deposit in Huayangchuan, located in the north Qinling Orogenic Belt. Field observation, mineralogy and geochemical analysis on a suite of drillhole samples were conducted to decipher the mineralization mechanism and its relationship with carbonatite. Huayangchuan carbonatite samples mainly consist of calcite and augite with small volume of accessory minerals (e.g., allanite, fluorapatite, barite and celestite). Betafite [(Ca,U)2(Ti,Nb,Ta)2O6(OH)] is the major ore-bearing mineral in Huayangchuan deposit. The carbonatite shows high CaO, low MgO and alkali contents, which should be products to be differentiated from primary carbonatite (high MgO and alkali contents). The immiscibility and crystallization processes could explain the high CaO/(CaO + MgO + FeO) ratios and the enrichment of LILE. Numerical modeling also indicates positive ?18OSMOW (7.29 to 15.53) and negative ?13CPDB (?5.26 to ?10.08) shifts are induced by reduced sediments assimilation from source consistent with there being enriched Sr-Nd and low Mg isotopic compositions. LA-ICP-MS zircon U-Pb dating of Huayangchuan carbonatite yielded Triassic ages of 229 ± 3 Ma, which corresponds to the post-collision stage of Qinling Orogen during the middle-late Triassic. We then proposed that the recycling of subducted sediments and later re-melting of those materials in shallow mantle generated the Huayangchuan carbonatite and subsequently formed the Huayangchuan deposit. Fluorine concentration decrease, caused by fluorapatite crystallization, ultimately resulted in betafite mineralization.
New evidence from a calcite dolomite carbonatite dyke for the magmatic origin of the massive Bayan Obo ore bearing dolomite marble, Inner Mongolia China.
Le Bas, M.J., Xueming, Y., Taylor, R.N., Spiro, B., Milton, J.A., Peishan, Z.
New evidence from a calcite dolomite carbonatite dyke for the magmatic origin of the massive Bayan Obo ore bearing dolomite marble, Inner Mongolia, China.
Mineralogy and Petrology, Vol. 90, 3-4, pp. 223-248.
Geochimica et Cosmochimica Acta, Vol. 266, pp. 307-311.
United States, California, Africa, Morocco
metasomatism
Abstract: We investigate the potential to use concentrations and zoning patterns of phosphorus (P) in clinopyroxene as indicators of the rates of igneous and metasomatic processes, comparable to recent applications of P in olivine but applicable to more evolved rocks and lower temperatures of crystallization. Few high-P pyroxenes have been previously reported, and none have been analyzed in detail for the mechanism of P enrichment or the implications for mineral growth kinetics. Here, we report the discovery and characteristics of exotic phosphorus-rich secondary clinopyroxene in glassy pockets and veins in composite mantle xenoliths from the Cima Volcanic Field (California, USA) and the Middle Atlas Mountains (Morocco, West Africa). These glass-bearing xenoliths preserve evidence of melt infiltration events and the contrasting behavior of P in their pyroxene crystals constrains the different rates of reaction and extents of equilibration that characterized infiltration in each setting. We report optical petrography and chemical analysis of glasses and minerals for major elements by electron microprobe microanalyzer and trace elements by laser-ablation Inductively Coupled Plasma Mass Spectrometry. The Cima Volcanic Field specimen shows one end-member behavior, with unzoned P-rich clinopyroxene in a melt pocket. We attribute this occurrence to a slow crystallization process that occurred after the melt temperature reached near-equilibrium with the host rock and during which the P concentration in the melt was buffered by apatite saturation. In the Morocco xenolith, by contrast, clinopyroxene exhibits zonation with P increasing all the way to the rim, in contact with the glass. We ascribe this feature to a rapid growth process in which excess P was incorporated into the growing clinopyroxene from a diffusive boundary layer. We demonstrate quantitative agreement between the enrichment of P and other trace elements and their expected diffusion and partitioning behavior during rapid growth. We suggest that P has not been widely reported in clinopyroxene in large part because it has rarely been looked for and that its analysis offers considerable promise as a kinetic indicator both in xenoliths and volcanic rocks.
