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SDLRC - Scientific Articles all years by Author - Q
The Sheahan Diamond Literature Reference Compilation
The Sheahan Diamond Literature Reference Compilation is compiled by Patricia Sheahan who publishes on a monthly basis a list of new scientific articles related to diamonds as well as media coverage and corporate announcementscalled the Sheahan Diamond Literature Service that is distributed as a free pdf to a list of followers. Pat has kindly agreed to allow her work to be made available as an online digital resource at Kaiser Research Online so that a broader community interested in diamonds and related geology can benefit. The references are for personal use information purposes only; when available a link is provided to an online location where the full article can be accessed or purchased directly. Reproduction of this compilation in part or in whole without permission from the Sheahan Diamond Literature Service is strictly prohibited. Return to Diamond Resource Center
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
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Abstract: Accurately dating the formation and modification of Earth’s sub-cratonic mantle still faces many challenges, primarily due to the long and complex history of depletion and subsequent metasomatism of this reservoir. In an attempt to improve this, we carried out the first study on peridotites from the Kaapvaal craton (Finsch Mine) that integrates results from Re-Os, Lu-Hf, Sm-Nd and Sr-isotope systems together with analyses of major-, trace- and platinum-group elements. The Finsch peridotites are well-suited for such a study because certain compositional features reflect they were highly depleted residues of shallow melting (1.5?GPa) at ambient Archean mantle temperatures. Yet, many of them have overabundant orthopyroxene, garnet and clinopyroxene compared to expected modal amounts for residues from partial melting. Finsch peridotites exhibit a wide range of rhenium depletion ages (TRD) from present day to 2.7?Ga, with a prominent mode at 2.5?Ga. This age overlaps well with a Lu-Hf isochron of 2.64?Ga (?Hf (t)?=?+26) which records silico-carbonatitic metasomatism of the refractory residues. This late Archean metasomatism is manifested by positive correlations of Pt/Ir and Pd/Ir with 187Os/188Os ratios and good correlations of modal amounts of silicates, especially garnet, with Os isotope ratios. These correlations suggest that the Highly Siderophile Elements (HSE) and incompatible element reenrichment and modal metasomatism result from one single major metasomatic event at late Archean. Our detailed study of Finsch peridotites highlights the importance of using multiple isotopic systems, to constrain the ages of events defining the evolution of lithospheric mantle. The Re-Os isotope system is very effective in documenting the presence of Archean lithosphere, but only the oldest TRD ages may accurately date or closely approach the age of the last major partial melting event. For a meaningful interpretation of the Re-Os isotope systematics the data must be combined with HSE patterns, trace-element compositions and ideally other isotopic systems, e.g. Lu-Hf. This is highlighted by the widespread evidence in Finsch peridotites of Pt, Pd and Re enrichment through significant Base Metal Sulfide (BMS) addition (mainly in the range of 0.002-0.08?wt%) that systematically shifts the mode of TRD model ages to younger ages.
Abstract: Natural emeralds from 11 mining areas were studied using an infrared spectrometer. The results showed different spectroscopic characteristics for emerald from different mine regions. Infrared absorption is mainly attributed to the vibration of Si-O lattice, channel water, alkaline cations, and molecules such as CO2, [Fe2(OH)4]2+, etc. Both near-infrared and mid-infrared spectra showed that the differences in band positions, intensities, and shapes are related to the mixed ratio of the two types of channel water. Accordingly, emerald and its mining regions can be divided into 3 types: H2O I, H2O II, and transition I-II. Furthermore, the study indicates that the relative amounts of the two different orientations of channel water molecules are mainly affected by the presence of (Mg + Fe)2+ in the host rock or in the mineralizing fluid. Therefore, the mineralization environment type (alkali-poor, alkali-rich, and transitional types) of emerald can be preliminarily identified from IR spectroscopy. This can be useful for determining the origin of emeralds.
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: At the Davdar mine in Xinjiang, north-western China, emeralds are hosted mainly by carbonate, quartz-carbonate and quartz veins cutting metasedimentary rocks, and are associated with minerals such as hematite, dolomite, quartz, orthoclase and albite. Sixteen rough emeralds obtained during the authors’ visit to the mining area in 2019 were studied by standard gemmolog-ical techniques and various spectroscopic methods (FTIR, Raman, UV-Vis-NIR and EPR), as well as LA-ICP-MS chemical analysis. The analysed samples were mostly coloured by Cr, and showed a wide range of Fe, V, Mg and alkali contents, along with relatively low Cs, Rb and Sc. UV-Vis-NIR spectra showed features at 370 nm (Fe3+), 430 nm (Cr3+ with contributions from V3+ and possibly Fe3+), 580-630 nm (Cr3+ and V3+), 638 and 683 nm (Cr3+), and 850 nm (Fe2+ and possibly Fe2+-Fe3+interactions). In addition, the more V-rich emeralds displayed a distinct V3+ absorption band at about 385-395 nm. Notably, the chemical composition of Davdar emeralds shows significant overlap with those from Panjshir, Afghanistan.
Geochimica et Cosmochimica Acta, Vol. 248, pp. 1-13.
Russia, Siberia
carbonatite
Abstract: Ca isotopes can be strongly fractionated at the Earth’s surface and thus may be tracers of subducted carbonates and other Ca-rich surface materials in mantle rocks, magmas and fluids. However, the ?44/40Ca range in the mantle and the scope of intra-mantle isotope fractionation are poorly constrained. We report Ca isotope analyses for 22 mantle xenoliths: four basalt-hosted refractory peridotites from Tariat in Mongolia and 18 samples from the Obnazhennaya (Obn) kimberlite on the NE Siberian craton. Obn peridotites are Paleoproterozoic to Archean melting residues metasomatised by carbonate-rich and/or silicate melts including unique xenoliths that contain texturally equilibrated carbonates. ?44/40Ca in 15 Obn xenoliths shows limited variation (0.74-0.97‰) that overlaps the value (0.94?±?0.05‰) inferred for the bulk silicate Earth from data on fertile lherzolites, but is lower than ?44/40Ca for non-metasomatised refractory peridotites from Mongolia (1.10?±?0.03‰). Bulk ?44/40Ca in four Obn peridotites containing metasomatic carbonates ranges from 0.81?±?0.08‰ to 0.83?±?0.06‰, with similar values in acid-leachates and leaching residues, indicating isotopic equilibration of the carbonates with host rocks. We infer that (a) metasomatism tends to decrease ?44/40Ca values of the mantle, but its effects are usually limited (?0.3‰); (b) Ca isotopes cannot distinguish "carbonatite" and "silicate" types of mantle metasomatism. The lowest ?44/40Ca value (0.56‰) was obtained for a phlogopite-bearing Obn peridotite with a very high Ca/Al of 8 suggesting that the greatest metasomatism-induced Ca isotope shifts may be seen in rocks initially low in Ca that experienced significant Ca input leading to high Ca/Al. Two Obn peridotites, a dunite (melt channel material) and a veined spinel wehrlite, have high ?44/40Ca values (1.22‰ and 1.38‰), which may be due to isotope fractionation by diffusion during silicate melt intrusion and percolation in the host mantle. Overall, we find no evidence that recycling of crustal carbonates may greatly affect Ca isotope values in the global mantle or on a regional scale.
Geochimica et Cosmochimica Acta, Vol. 248, pp. 1-13.
Mantle
carbonatite
Abstract: Ca isotopes can be strongly fractionated at the Earth’s surface and thus may be tracers of subducted carbonates and other Ca-rich surface materials in mantle rocks, magmas and fluids. However, the ?44/40Ca range in the mantle and the scope of intra-mantle isotope fractionation are poorly constrained. We report Ca isotope analyses for 22 mantle xenoliths: four basalt-hosted refractory peridotites from Tariat in Mongolia and 18 samples from the Obnazhennaya (Obn) kimberlite on the NE Siberian craton. Obn peridotites are Paleoproterozoic to Archean melting residues metasomatised by carbonate-rich and/or silicate melts including unique xenoliths that contain texturally equilibrated carbonates. ?44/40Ca in 15 Obn xenoliths shows limited variation (0.74-0.97‰) that overlaps the value (0.94?±?0.05‰) inferred for the bulk silicate Earth from data on fertile lherzolites, but is lower than ?44/40Ca for non-metasomatised refractory peridotites from Mongolia (1.10?±?0.03‰). Bulk ?44/40Ca in four Obn peridotites containing metasomatic carbonates ranges from 0.81?±?0.08‰ to 0.83?±?0.06‰, with similar values in acid-leachates and leaching residues, indicating isotopic equilibration of the carbonates with host rocks. We infer that (a) metasomatism tends to decrease ?44/40Ca values of the mantle, but its effects are usually limited (?0.3‰); (b) Ca isotopes cannot distinguish "carbonatite" and "silicate" types of mantle metasomatism. The lowest ?44/40Ca value (0.56‰) was obtained for a phlogopite-bearing Obn peridotite with a very high Ca/Al of 8 suggesting that the greatest metasomatism-induced Ca isotope shifts may be seen in rocks initially low in Ca that experienced significant Ca input leading to high Ca/Al. Two Obn peridotites, a dunite (melt channel material) and a veined spinel wehrlite, have high ?44/40Ca values (1.22‰ and 1.38‰), which may be due to isotope fractionation by diffusion during silicate melt intrusion and percolation in the host mantle. Overall, we find no evidence that recycling of crustal carbonates may greatly affect Ca isotope values in the global mantle or on a regional scale.
Geochimica et Cosmochimica Acta, Vol. 248, pp. 1-13.
Mantle, Asia, Mongolia, Russia, Siberia
metasomatism
Abstract: Ca isotopes can be strongly fractionated at the Earth’s surface and thus may be tracers of subducted carbonates and other Ca-rich surface materials in mantle rocks, magmas and fluids. However, the ?44/40Ca range in the mantle and the scope of intra-mantle isotope fractionation are poorly constrained. We report Ca isotope analyses for 22 mantle xenoliths: four basalt-hosted refractory peridotites from Tariat in Mongolia and 18 samples from the Obnazhennaya (Obn) kimberlite on the NE Siberian craton. Obn peridotites are Paleoproterozoic to Archean melting residues metasomatised by carbonate-rich and/or silicate melts including unique xenoliths that contain texturally equilibrated carbonates. ?44/40Ca in 15 Obn xenoliths shows limited variation (0.74-0.97‰) that overlaps the value (0.94?±?0.05‰) inferred for the bulk silicate Earth from data on fertile lherzolites, but is lower than ?44/40Ca for non-metasomatised refractory peridotites from Mongolia (1.10?±?0.03‰). Bulk ?44/40Ca in four Obn peridotites containing metasomatic carbonates ranges from 0.81?±?0.08‰ to 0.83?±?0.06‰, with similar values in acid-leachates and leaching residues, indicating isotopic equilibration of the carbonates with host rocks. We infer that (a) metasomatism tends to decrease ?44/40Ca values of the mantle, but its effects are usually limited (?0.3‰); (b) Ca isotopes cannot distinguish “carbonatite” and “silicate” types of mantle metasomatism. The lowest ?44/40Ca value (0.56‰) was obtained for a phlogopite-bearing Obn peridotite with a very high Ca/Al of 8 suggesting that the greatest metasomatism-induced Ca isotope shifts may be seen in rocks initially low in Ca that experienced significant Ca input leading to high Ca/Al. Two Obn peridotites, a dunite (melt channel material) and a veined spinel wehrlite, have high ?44/40Ca values (1.22‰ and 1.38‰), which may be due to isotope fractionation by diffusion during silicate melt intrusion and percolation in the host mantle. Overall, we find no evidence that recycling of crustal carbonates may greatly affect Ca isotope values in the global mantle or on a regional scale.
Metamorphic evolution of medium temperatire ultra high pressure ( MT-UHP) eclogites from the South Dabie orogen, central China: an insight from phase equilibration temperatures modelling.
Journal of Metamorphic Geology, Vol. 31, 7, pp. 755-774,
Abstract: A method for detecting large-size diamonds with low content in a complex mixture was described. Phase identification via conventional X-ray diffraction method is unsuitable because of the large-size and low-content characteristics of the diamonds. Thus, we proposed a convenient approach (i.e., rocking scan) for assessing the presence of low-content diamonds in a complex mixture. A thorough rocking scan of the (111), (220), and (311) planes revealed the presence of low-content diamonds prepared by reducing dense carbon dioxide with alkali metals. This procedure can be successfully applied to several standard mixture samples prepared by mixing ?-SiO2, ?-Al2O3, graphite, and pure diamond powders, which are commercially available. We estimated that the detection limit was at or below the 0.1?wt% level by using the proposed method under the current condition. This method is straightforward, routinized, and may be specifically developed to satisfy the requirements of public and private institutions for a rapid identification of other mixture phases, of which the large-size and low-content characteristics do not allow an instant phase identification by conventional X-ray diffraction methods.
Abstract: Natural emeralds from 11 mining areas were studied using an infrared spectrometer. The results showed different spectroscopic characteristics for emerald from different mine regions. Infrared absorption is mainly attributed to the vibration of Si-O lattice, channel water, alkaline cations, and molecules such as CO2, [Fe2(OH)4]2+, etc. Both near-infrared and mid-infrared spectra showed that the differences in band positions, intensities, and shapes are related to the mixed ratio of the two types of channel water. Accordingly, emerald and its mining regions can be divided into 3 types: H2O I, H2O II, and transition I-II. Furthermore, the study indicates that the relative amounts of the two different orientations of channel water molecules are mainly affected by the presence of (Mg + Fe)2+ in the host rock or in the mineralizing fluid. Therefore, the mineralization environment type (alkali-poor, alkali-rich, and transitional types) of emerald can be preliminarily identified from IR spectroscopy. This can be useful for determining the origin of emeralds.
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.
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.
Pure and Applied Physics, Vol. 177, pp. 5263-5274.
Mantle
geophysics - magnetics
Abstract: Theoretical magnetotelluric (MT) soundings are investigated for a stratified (five-layered) Earth model consisting of two transitional layers with conductivity varying linearly with depth, and three homogeneous layers with constant conductivity. The analytical expressions for the tangential electric and magnetic fields as well as the surface impedance are derived in terms of Airy functions. The effect of the thicknesses of the two transitional layers and the interlayer between them on the MT responses (apparent resistivity and impedance phase) is examined in detail.
Earth and Planetary Science Letters, Vol. 474, pp. 128-137.
Mantle
peridotites
Abstract: To better constrain the Ca isotopic composition of the Bulk Silicate Earth (BSE) and explore the Ca isotope fractionation in the mantle, we determined the Ca isotopic composition of 28 peridotite xenoliths from Mongolia, southern Siberia and the Siberian craton. The samples are divided in three chemical groups: (1) fertile, unmetasomatized lherzolites (3.7-4.7 wt.% Al2O3); (2) moderately melt-depleted peridotites (1.3-3.0 wt.% Al2O3) with no or very limited metasomatism (LREE-depleted cpx); (3) strongly metasomatized peridotites (LREE-enriched cpx and bulk rock) further divided in subgroups 3a (harzburgites, 0.1-1.0% Al2O3) and 3b (fertile lherzolites, 3.9-4.3% Al2O3). In Group 1, ?44/40Ca of fertile spinel and garnet peridotites, which experienced little or no melting and metasomatism, show a limited variation from 0.90 to 0.99‰ (relative to SRM 915a) and an average of 0.94 ± 0.05‰ (2SD, ), which defines the Ca isotopic composition of the BSE. In Group 2, the ?44/40Ca is the highest for three rocks with the lowest Al2O3, i.e. the greatest melt extraction degrees (average ‰, i.e. ?0.1‰ heavier than the BSE estimate). Simple modeling of modal melting shows that partial melting of the BSE with ranging from 0.10 to 0.25 can explain the Group 2 data. By contrast, ?44/40Ca in eight out of nine metasomatized Group 3 peridotites are lower than the BSE estimate. The Group 3a harzburgites show the greatest ?44/40Ca variation range (0.25-0.96‰), with ?44/40Ca positively correlated with CaO and negatively correlated with Ce/Eu. Chemical evidence suggests that the residual, melt-depleted, low-Ca protoliths of the Group 3a harzburgites were metasomatized, likely by carbonate-rich melts/fluids. We argue that such fluids may have low (?0.25‰) ?44/40Ca either because they contain recycled crustal components or because Ca isotopes, similar to trace elements and their ratios, may be fractionated by kinetic and/or chromatographic effects of melt percolation in the mantle. The ?44/40Ca in Group 3b lherzolites (0.83-0.89‰) are lower than in the BSE as well, but the effects of metasomatism on ?44/40Ca are smaller, possibly because of the high Ca contents in their protoliths and/or smaller ?44/40Ca differences between the protoliths and metasomatic agents. The BSE estimates based on fertile peridotites in this study fall in the ?44/40Ca ranges for oceanic and continental basalts, various meteorites (achondrites; carbonaceous, ordinary and enstatite chondrites), Mars, and the Moon. These results provide benchmarks for the application of Ca isotopes to planet formation, mantle evolution, and crustal recycling.
Science China Earth Sciences, Vol. 60, 2, pp. 207-217.
Technology
Subduction
Abstract: Diamonds are renowned as the record of Earth’s evolution history. Natural diamonds on the Earth can be distinguished in light of genetic types as kimberlitic diamonds (including peridotitic diamonds and eclogitic diamonds), ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds. According to the inclusion mineralogy, most diamonds originated from continental lithospheric mantle at depths of 140-250 km. Several localities, however, yield ultradeep diamonds with inclusion compositions that require a sublithospheric origin (>~250 km). Ultradeep diamonds exhibit distinctions in terms of carbon isotope composition, N-concentration, mineral inclusions and so on. The present study provides a systematic compilation concerning the features of ultradeep diamonds, based on which to expound their genesis affinity with mantle-carbonate melts. The diamond-parental carbonate melts are proposed to be stemmed from the Earth’s crust through subduction of oceanic lithosphere. Ultradeep diamonds are classified into a subgroup attaching to kimberlitic diamonds grounded by formation mechanism, and present connections in respect of carbon origin to eclogitic diamonds, ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds.
Abstract: Diamonds are renowned as the record of Earth’s evolution history. Natural diamonds on the Earth can be distinguished in light of genetic types as kimberlitic diamonds (including peridotitic diamonds and eclogitic diamonds), ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds. According to the inclusion mineralogy, most diamonds originated from continental lithospheric mantle at depths of 140-250 km. Several localities, however, yield ultradeep diamonds with inclusion compositions that require a sublithospheric origin (>~250 km). Ultradeep diamonds exhibit distinctions in terms of carbon isotope composition, N-concentration, mineral inclusions and so on. The present study provides a systematic compilation concerning the features of ultradeep diamonds, based on which to expound their genesis affinity with mantle-carbonate melts. The diamond-parental carbonate melts are proposed to be stemmed from the Earth’s crust through subduction of oceanic lithosphere. Ultradeep diamonds are classified into a subgroup attaching to kimberlitic diamonds grounded by formation mechanism, and present connections in respect of carbon origin to eclogitic diamonds, ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds.
Abstract: Diamonds are renowned as the record of Earth’s evolution history. Natural diamonds on the Earth can be distinguished in light of genetic types as kimberlitic diamonds (including peridotitic diamonds and eclogitic diamonds), ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds. According to the inclusion mineralogy, most diamonds originated from continental lithospheric mantle at depths of 140–250 km. Several localities, however, yield ultradeep diamonds with inclusion compositions that require a sublithospheric origin (>~250 km). Ultradeep diamonds exhibit distinctions in terms of carbon isotope composition, N-concentration, mineral inclusions and so on. The present study provides a systematic compilation concerning the features of ultradeep diamonds, based on which to expound their genesis affinity with mantle-carbonate melts. The diamond-parental carbonate melts are proposed to be stemmed from the Earth’s crust through subduction of oceanic lithosphere. Ultradeep diamonds are classified into a subgroup attaching to kimberlitic diamonds grounded by formation mechanism, and present connections in respect of carbon origin to eclogitic diamonds, ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds.
Contributions to Mineralogy and Petrology, 10.1007/ s00410-018-1478-x 10p.
Mantle
melting
Abstract: Ni, Co, and Zn are widely distributed in the Earth’s mantle as significant minor elements that may offer insights into the chemistry of melting in the mantle. To better understand the distribution of Ni2+, Co2+, and Zn2+ in the most abundant silicate phases in the transition zone and the upper mantle, we have analyzed the crystal chemistry of wadsleyite (Mg2SiO4), ringwoodite (Mg2SiO4), forsterite (Mg2SiO4), and clinoenstatite (Mg2Si2O6) synthesized at 12-20 GPa and 1200-1400 °C with 1.5-3 wt% of either NiO, CoO, or ZnO in starting materials. Single-crystal X-ray diffraction analyses demonstrate that significant amounts of Ni, Co, and Zn are incorporated in octahedral sites in wadsleyite (up to 7.1 at%), ringwoodite (up to 11.3 at%), olivine (up to 2.0 at%), and clinoenstatite (up to 3.2 at%). Crystal structure refinements indicate that crystal field stabilization energy (CFSE) controls both cation ordering and transition metal partitioning in coexisting minerals. According to electron microprobe analyses, Ni and Co partition preferentially into forsterite and wadsleyite relative to coexisting clinoenstatite. Ni strongly prefers ringwoodite over coexisting wadsleyite with DRw/WdNi?=?4.13. Due to decreasing metal-oxygen distances with rising pressure, crystal field effect on distribution of divalent metal ions in magnesium silicates is more critical in the transition zone relative to the upper mantle. Analyses of Ni partitioning between the major upper-mantle phases implies that Ni-rich olivine in ultramafic rocks can be indicative of near-primary magmas.
Earth and Planetary Science Letters, Vol. 520, pp. 164-174.
Mantle
diamond genesis
Abstract: To better understand the role of sulfide in C storage in the upper mantle, we construct a thermodynamic model for Fe-Ni-S-C sulfide melts and consider equilibrium between sulfide melts, mantle silicates, Fe-Ni alloy, and diamond. The sulfide melt model is based upon previous parameterization of Fe-Ni-S melts calibrated at 100 kPa, which we have extended to high pressure based on volumetric properties of end-member components. We calculate the behavior of C in the sulfide melt from empirical parameterization of experimental C solubility data. We calculate the continuous compositional evolution of Fe-Ni sulfide liquid and associated effects on carbon storage at pressure and redox conditions corresponding to mantle depths of 60 to 410 km. Equilibrium and mass balance conditions were solved for coexisting Fe-Ni-S melt and silicate minerals (olivine [(Mg,Fe,Ni)2SiO4], pyroxene [(Mg,Fe)SiO3]) in a mantle with 200 ppmw S. With increasing depth and decreasing oxygen fugacity (fO2), the calculated melt (Fe+Ni)/S atomic ratio increases from 0.8-1.5 in the shallow oxidized mantle to 2.0-10.5 in the reduced deep upper mantle (>8 GPa), with Fe-Ni alloy saturation occurring at >10 GPa. Compared to previous calculations for the reduced deep upper mantle, alloy saturation occurs at greater depth owing to the capacity of sulfide melt to dissolve metal species, thereby attenuating the rise of Fe and Ni metal activities. The corresponding carbon storage capacity in the metal-rich sulfide liquid rises from negligible below 6 GPa to 8-20 ppmw at 9 GPa, and thence increases sharply to 90-110 ppmw at the point of alloy saturation at 10-12 GPa. The combined C storage capacity of liquid and solid alloy reaches 110-170 ppmw at 14 GPa. Thus, in the deep upper mantle, all carbon in depleted sources (10-30 ppmw C) can be stored in the sulfide liquid, and alloy and sulfide liquids host a significant fraction of the C in enriched sources (30-500 ppmw C). Application of these results to the occurrences of inferred metal-rich sulfide melts in the Fe-Ni-S-C system and inclusions in diamonds from the mantle transition zone suggests that oxidization of a reduced metal-rich sulfide melt is an efficient mechanism for deep-mantle diamond precipitation, owing to the strong effect of (Fe+Ni)/S ratio on carbon solubility in Fe-Ni-S melts. This redox reaction likely occurs near the boundary between oxidized subducted slabs and the reduced ambient peridotitic mantle.
Diamond & Related Materials, in press available, 34p. Pdf
Global
boron
Abstract: The polycrystalline diamond compact (PDC), which consists of a polycrystalline diamond layer on a tungsten carbide (WC)/cobalt (Co) substrate, is extensively utilized as drilling bits. However, the poor thermal stability due to the graphitization and oxygen susceptibility of diamond severely limits the application of PDCs to high-temperature drilling work. In this study, a new PDC with improved thermal stability is successfully synthesized with boron (B)-coated diamond particles, which forms a uniform boron carbide (B4C) barrier. The as-received B4C phase acts as a protective barrier, which enhances the initial graphitization and oxidizing temperatures to 800 °C and 780 °C, respectively, which are ~100 °C and ~30 °C higher than those (700 °C and 750 °C) of the PDC sintered with uncoated diamond particles. The B4C barrier protects diamond grains from direct contact with the Co phase, prohibiting the cobalt-catalytic graphitization. In addition, the oxidation of the B4C barrier occurs prior to that of the diamond grains, which inhibits the PDC from oxidation.
Abstract: Regolith-hosted rare earth element (REE) deposits predominate global resources of heavy REEs. Regoliths are underlain by various types of igneous rocks and do not always host economically valuable deposits. Thus a feasible and convenient method is desired to identify REE mineralization in a particular regolith. This study presents a detailed visible short-wave infrared reflectance (VSWIR) spectroscopic study of the Renju regolith-hosted REE deposit, South China, to provide diagnostic parameters for targeting REE orebodies in regoliths. The results show that the spectral parameters, M794_2nd and M800_2nd, derived from the VSWIR absorption of Nd3+ at approximately 800 nm, can be effectively used to estimate the total REE concentrations in regolith profiles. M1396_2nd/M1910_2nd ratios can serve as proxies to evaluate weathering intensities in a regolith. Abrupt changes of specific spectral features related to mineral abundances, chemical compositions, and weathering intensities can be correlated with variations of protolith that formed a regolith. These VSWIR proxies are robust and can be used for exploration of regolith-hosted REE deposits.
Abstract: Carbonatites and related alkaline rocks host most REE resources. Phosphate minerals, e.g., apatite and monazite, commonly occur as the main REE-host in carbonatites and have been used for tracing magmatic and mineralization processes. Many carbonatite intrusions undergo metamorphic and/or metasomatic modification after emplacement; however, the effects of such secondary events are controversial. In this study, the Miaoya and Shaxiongdong carbonatite-alkaline complexes, in the South Qinling Belt of Central China, are selected to unravel their magmatic and hydrothermal remobilization histories. Both the complexes are accompanied by Nb-REE mineralization and contain apatite and monazite-(Ce) as the major REE carriers. Apatite grains from the two complexes commonly show typical replacement textures related to fluid metasomatism, due to coupled dissolution-reprecipitation. The altered apatite domains, which contain abundant monazite-(Ce) inclusions or are locally surrounded by fine-grained monazite-(Ce), have average REE concentrations lower than primary apatite. These monazite-(Ce) inclusions and fine-grained monazite-(Ce) grains are proposed to have formed by the leaching REE from primary apatite grains during fluid metasomatism. A second type of monazite-(Ce), not spatially associated with apatite, shows porous textures and zoning under BSE imaging. Spot analyses of these monazite-(Ce) grains have variable U-Th-Pb ages of 210-410 Ma and show a peak age of 230 Ma, which is significantly younger than the emplacement age (440-430 Ma) but is roughly synchronous with a regionally metamorphic event related to the collision between the North China Craton and Yangtze Block along the Mianlue suture. However, in situ LA-MC-ICP-MS analyses of those grains show that they have initial Nd values same as those of magmatic apatite and whole rock. We suggest these monazite-(Ce) grains crystallized from the early Silurian carbonatites and have been partially or fully modified during a Triassic metamorphic event, partially resetting U-Pb ages over a wide range. Mass-balance calculations, based on mass proportions and the REE contents of monazite-(Ce) and apatite, demonstrate that the quantity of metasomatized early Silurian monazite-(Ce) is far higher than the proportion of monazite-(Ce) resulting from the metasomatic alteration of the apatite. Therefore, Triassic metamorphic events largely reset the U-Th-Pb isotopic system of the primary monazite-(Ce) and apatite but only had limited or local effects on REE remobilization in the carbonatite-alkaline complexes in the South Qinling Belt. Such scenarios may be widely applicable for other carbonatite and hydrothermal systems.
Deep subduction of continental crust in accretionary orogen: evidence from U-Pb dating on diamond-bearing zircons from the Qinling orogen, central China.
Abstract: Although REE (lanthanides + Sc + Y) mineralization in alkaline silicate systems is commonly accompanied with Zr mineralization worldwide, our understanding of the relationship between Zr and REE mineralization is still incomplete. The Baerzhe deposit in Northeastern China is a reservoir of REE, Nb, Zr, and Be linked to the formation of an Early Cretaceous, silica-saturated, alkaline intrusive complex. In this study, we use in situ laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) analyses of zircon and monazite crystals to constrain the relationship between Zr and REE mineralization at Baerzhe. Three groups of zircon are identified and are differentiated based upon textural observations and compositional characteristics. Type Ia zircons display well-developed oscillatory zoning. Type Ib zircons are darker in cathodoluminescence images and have more irregular zoning and resorption features than type Ia zircons. In addition, type Ib zircons can locally occur as overgrowths on type Ia zircons. Type II zircons contain irregular but translucent cores and rims with oscillatory zoning that are murky brown in color and occur in aggregates. Textural features and compositional data suggest that types Ia and Ib zircon crystallized at the magmatic stage, with type Ia being least-altered and type Ib being strongly altered. Type II zircons, on the other hand, precipitated during the magmatic to magmatichydrothermal transition. Whereas the magnitude of the Eu anomaly is moderate in the barren alkaline granite, both magmatic and deuteric zircon exhibit pronounced negative anomalies. Such features are difficult to explain exclusively by feldspar fractionation and could indicate the presence of fluid induced modification of the rocks. Monazite crystals occur mostly through replacement of zircon and sodic amphibole; monazite clusters are also present. Textural and compositional evidence suggests that monazite at Baerzhe is hydrothermal. Types Ia and Ib magmatic zircon yield 207Pb-corrected 206Pb/238U ages of 127.2 ± 1.3 and 125.4 ± 0.7 Ma, respectively. Type II deuteric zircon precipitated at 124.9 ± 0.6 Ma. The chronological data suggest that the magmatic stage of the highly evolved Baerzhe alkaline granite lasted less than two million years. Hydrothermal monazite records a REE mineralization event at 122.8 ± 0.6 Ma, approximately 1 or 2 million years after Zr mineralization. We therefore propose a model in which parental magmas of the Baerzhe pluton underwent extensive magmatic differentiation while residual melts interacted with aqueous hydrothermal fluids. Deuteric zircon precipitated from a hydrosilicate liquid, and subsequent REE mineralization, exemplified by hydrothermal monazite, correlates with hydrothermal metasomatic alteration that postdated the hydrosilicate liquid event. Such interplay between magmatic and hydrothermal processes resulted in the formation of discrete Zr and REE mineralization at Baerzhe.
Journal of African Sciences, Vol. 184, 104308, 12p. Pdf
Africa, Tanzania
deposit - Mbalizi
Abstract: The Mbalizi carbonatite is located in the middle of the Paleoproterozoic Ubendian Mobile Belt and the western branch of East Africa Rift, southwestern Tanzania. Calcite, dolomite, phlogopite, pyrochlore and apatite are found in the sample. Mineral chemistry studies have shown that the carbonatite phlogopite is linked to mantle-derived magmatism. The apatite is fluorapatite, means they are of magmatic origin. The analyses on two crystals of pyrochlore show high concentrations of Nb2O5, and therefore the Nb-oxide is classified as pyrochlore subspecies. Three types of zircon have been obtained from the Mbalizi carbonatite, including xenocrysts zircon, igneous zircon and metamorphic zircon. Zircon in-situ LA-ICP-MS U-Pb dating in this contribution indicates that the Mbalizi carbonatite was crystallized at ca. 116.0 ± 1.8 Ma. The ?Hf(t) values of igneous zircon ranging from ?13.9 to +5.7, indicates that the carbonatite parental magma was originated from the sub-continental lithospheric mantle, and evolves toward HIMU and EM. The whole-rock Sr-Nd isotopic data suggest more contribution of the HIMU and EM? material. We propose that the complex evolutionary history of the Ubendian Mobile Belt has stored the subduction oceanic crust which has the EM? and HIMU components, forming the compositional heterogeneity mantle beneath the Ubendian Mobile Belt. At 116.0 ± 1.8 Ma, with the extension stress field, deep faults cause the pressure reduction, resulting in reactive of the upwelling of the HIMU and EM? components. This provides the metamorphic conditions to induce the isotopic resetting and may result in large scatter of initial 176Hf/177Hf ratios of carbonatite melts.
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 × 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.
Abstract: Geophysical investigations and laboratory experiments show evidence for possible subduction of ancient oceanic crust. Geological and mineralogical observations suggest that subducted oceanic crust is recycled into the upper mantle. The subduction is supported by the recovery of super?deep diamonds from kimberlites and the presence of crustal materials in ophiolitic chromitites and their host peridotites. What is the mechanism? Here we report the new discovery of ophiolite?hosted diamonds in the podiform chromitites within the Skenderbeu massif from the Mirdita ophiolite in the western part of Neo?Tethys (Fig. 1). The diamonds are characterized by exceedingly light C isotopes (?13CPDB ? ?25‰), which can be interpreted as evidence for subduction of organic carbon from Earth's surface. The diamonds are also characterized by an exceptionally large range in ?15Nair (?12.9‰ to +25.5‰), accompanied by a low N aggregation state (Fig. 2). On the other hand, materials sparsely included in diamonds include amorphous material, Ni?Mn?Co alloy, nanocrystals (20 nm×20 nm) of calcium silicate with an orthorhombic perovskite structure (Ca?Pv), and fluids (Fig. 3). We consider 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 environment. The environment is in the diamond stability field or near the top of the mantle transition zone. The new discovery of diamonds from the Mirdita ophiolite provides a valuable opportunity to understand deep cycling of subducted oceanic crust and mantle (i.e., composition and process).
Abstract: Farré?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, Farré?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: A colour-changing garnet exhibits the "alexandrite effect", whereby its colour changes from green in the presence of daylight to purplish red under incandescent light. This study examines this species of garnets as well as the causes of the colour change by using infrared and ultraviolet visible (UV-Vis) spectroscopy. The infrared spectra show that the colour-changing garnets in this paper belong to the solid solution of pyrope-spessartine type. CIE1931 XYZ colour matching functions are used to calculate the colour parameters influencing garnet colour-changing under different light sources. The UV-Vis spectra show two zones of transmittance, in the red region at 650-700 nm and the blue-green region at 460-510 nm. As they exhibit the same capacity to transmit light, the colour of the gem is determined by the external light source. The absorption bands of Cr3+ and V3+ at 574 nm in the UV-Vis spectra are the main cause of the change in colour. With the increase in the area of peak absorption, the differences in the chroma and colour of the garnet gradually increase in daylight and incandescent light, and it exhibits a more prominent colour-changing effect.
Neues Jahrbuch fur Mineralogie, Vol. 195, pp. 145-153.
Australia
deposit - Argyle
Abstract: Contact twinning with the so-called "macle" form or other shapes are often found in natural diamond crystals. However, the surface microtopographic features associated with twinning have been less investigated. Here, the surface dissolution and growth features seen on the twin boundaries, including the re-entrant angles revealed by differential interference contrast microscope and SEM techniques in 170 natural diamond crystals mainly from Argle mine, Australia are described and summarized. The hexagonal pits, rhombic pits along with higher symmetry observed at the twin boundaries together with dislocations and their formation processes are discussed.
Precisely dating Paleozoic kimberlites in the North Chin a craton and Hf isotopic constraints on the evolution of the subcontinental lithospheric mantle.
Precise age determin ation of the Paleozoic kimberlites in North Chin a craton and Hf isotopic constraint on the evolution of its subcontinental lithospheric mantle.
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 Earth’s 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 Earth’s 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.
Geostandards and Geoanalltical Research, Vol. 43, 3, pp. 543-565.
China, Europe, Sweden, Asia, Mongolia, United States, Africa, Malawi, Madagascar
REE
Abstract: Bastnäsite is the end member of a large group of carbonate-fluoride minerals with the common formula (REE) CO3F•CaCO3. 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 bastnäsite 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 bastnäsite 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 bastnäsite 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 bastnäsites 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.
Diamond & Related Materials, Vol. 81, pp. 161-167.
Technology
microdiamonds
Abstract: Polylactic acid (PLA)-based composites filled with 20 or 50 ?m-diameter microdiamond are synthesized by hot pressing. Through improving the interface compatibility between the filler and the matrix enabled by octadecylamine (ODA) coating on the microdiamond particles, the maximum thermal conductivity of the composites is 2.22 Wm? 1 K? 1, which is a ~ 10-fold increase in comparison with that of pure PLA. According to the analysis on the glass transmission of the composites and the surface chemistry of the fillers using DSC, FI-IR, and Raman microscopy, it is found out that ODA is connected with the -OH group on the microdiamond surface through hydrogen bonding and an interfacial structure of PLA/ODA/microdiamond is formed. Thus, the interfacial thermal transport between PLA and microdiamond is significantly improved, leading to the enhancement of the thermal conductivity of the composites. Our work presents a simple method to modify the surface chemistry of microdiamond and to improve the interface compatibility between microdiamond and PLA. The microdiamond/PLA composites with large thermal conductivity are promising thermal management materials used for modern electronic products.
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.
Comtrasting Group I and Group II eclogite xenolith petrogenesis: petrological, trace element and isotopic evidence from eclogite, garnet websterite and akremite
Journal of Petrology, Vol. 46, 10, Oct. pp. 2059-2090.
Abstract: Mineral inclusions in diamonds have been used to track potential information on the Earth's deep mantle. Here we report results from a detailed study on the mineral inclusions in a ca. 0.28 ct diamond from the Shengli No. 1 kimberlite in Mengyin County, Shandong Province, eastern China. Our study reveals the presence of ?-quartz, albite and olivine in the diamond. At an inferred depth of ca. 165 km for the diamond crystallization, the inclusions of ?-quartz and albite suggest the possible involvement of deep subducted crustal material, traces of which were captured during the diamond growth and magma migration.
Abstract: We present major and trace element compositions of mineral concentrates comprising garnet xenocrysts, ilmenite, phlogopite, spinel, zircon, and uncommon minerals (titanite, calzirtite, anatase, baddeleyite and pyrochlore) of a newly discovered Late Cretaceous kimberlite (U-Pb zircon age 90.0 ± 1.3 Ma; 2?) named Osvaldo França 1, located in the Alto Paranaíba Igneous Province (APIP), southeastern Brazil. Pyrope grains are lherzolitic (Lherz-1, Lherz-2 and Lherz-3), harzburgitic (Harz-3) and wehrlitic (Wehr-2). The pyrope xenocrysts cover a wide mantle column in the subcratonic lithosphere (66-143 km; 20-43 kbar) at relatively low temperatures (811-875 °C). The shallowest part of this mantle is represented by Lherz-1 pyropes (20-32 kbar), which have low-Cr (Cr2O3 = 1.74-6.89 wt.%) and fractionated middle to heavy rare earth elements (MREE-HREE) pattern. The deepest samples are represented by Lherz-2, Lherz-3, Harz-3, and Wehr-2 pyropes (36-43 kbar). They contain high-Cr contents (Cr2O3 = 7.36-11.19 wt.%) and are characterized by sinusoidal (Lherz-2 and Wehr-2) and spoon-like (Lherz-3 and Harz-3) REE patterns. According to their REE and trace elements, pyrope xenocrysts have enriched nature (e.g., Ce and Yb vs. Cr2O3), indicating that the cratonic lithosphere has been affected by a silicate melt with subalkaline/tholeiite composition due to their low Zr, Ti and Y concentrations. Besides minerals with typical kimberlitic signatures, such as ilmenite and zircon, the exotic compositions of phlogopite and ulvöspinel suggest an enriched component in the magma source. The formation of rare mineral phases with strong enrichment of light-REE (LREE) and high field strength elements (HFSE) is attributed to the late-stage kimberlitic melt. We propose a tectonic model where a thermal anomaly, represented by the low-velocity seismic anomaly observed in P-wave seismic tomography images, supplied heat to activate the alkaline magmatism from a metasomatized cratonic mantle source during the late-stages of Gondwana fragmentation and consequent South Atlantic Ocean opening. The metasomatism recorded by mineral phases is a product of long-lived recycling of subducted oceanic plates since the Neoproterozoic (Brasiliano Orogeny) or even older collisional events, contributing to the exotic character of the Osvaldo França 1 kimberlite, as well as to the cratonic lithospheric mantle.
Joint seismic geodynamic mineral physical modeling of African geodynamics: a reconciliation of deep mantle convection with surface geophysical constraints.
Earth and Planetary Science Letters, Vol. 295, 3-4, pp. 329-341.
Abstract: Over the past three decades, it has become clear that Pangea was just the most recent of several supercontinents that have amalgamated and dispersed since at least 2.0 Ga. It was fully recognized at the time that the so-called "supercontinent cycle" had a profound effect on Earth Systems, possibly one of the most significant insights since the advent of plate tectonics. In the early 1980's, Damian Nance, along with colleagues Tom Worsley and Judith Moody, were the instigators of this phase of modern thinking and since that time so many international projects and research careers have been spawned by those insights. Although many elegant papers had proposed orogenic episodicity before the acceptance of the plate tectonic paradigm, Damian and colleagues were the first to link such episodicity to a supercontinent cycle. In addition, Damian has made seminal contributions to the understanding of orogenic processes in general, and through his detailed fieldwork, to our foundational knowledge of the geology of the Avalonian belt in Maritime Canada, Paleozoic and Proterozoic complexes in Mexico, recent (Quaternary) tectonics in Greece and even more recent Beam Engine tectonics in Cornwall and the rest of the world. His body of work has had first-order implications for the interpretation of ancient orogens and the processes responsible for them. Most important of all, we have all benefited from the positive impact Damian has had on all our careers and the generosity and collegial approach to research. His influence has extended far beyond his immediate research community as a result of his co-leadership of IGCP projects and his inclusive approach to sharing and developing new avenues in science. He has inspired generations of students and his peers and his legacy is immense.
Geological Society of America Bulletin, Vol. 133, 3/4, pp. 625-646. pdf
Global
Pangea
Abstract: The supercontinent Pangea formed by the subduction of the Iapetus and Rheic oceans between Gondwana, Laurentia, and Baltica during mid-to-late Paleozoic times. However, there remains much debate regarding how this amalgamation was achieved. Most paleogeographic models based on paleomagnetic data argue that the juxtaposition of Gondwana and Laurussia (Laurentia-Baltica) was achieved via long-lasting highly oblique convergence in the late Paleozoic. In contrast, many geology-based reconstructions suggest that the collision between the two continents was likely initiated via a Gondwanan promontory comprising the Iberian, Armorican, and Bohemian massifs, and parts of the basement units in the Alpine orogen during the Early Devonian. To help resolve this discrepancy, we present an updated compilation of high-quality paleopoles of mid-to-late Paleozoic ages (spanning Middle Ordovician and Carboniferous times) from Gondwana, Laurentia, and Baltica. These paleopoles were evaluated with the Van der Voo selection criteria, corrected for inclination error where necessary, and were used to revise their apparent polar wander (APW) paths. The revised APW paths were constructed using an innovative approach in which age errors, A95 ovals, and Q-factors of individual paleopoles are taken into account. By combining the resulting APW paths with existing geological data and field relationships in the European Variscides, we provide mid-to-late Paleozoic paleogeographic reconstructions which indicate that the formation of Pangea was likely initiated at 400 Ma via the collision between Laurussia and a ribbon-like Gondwanan promontory that was itself formed by a scissor-like opening of the Paleotethys Ocean, and that the amalgamation culminated in the mostly orthogonal convergence between Gondwana and Laurussia.
Journal of Geochemical Exploration, Vol. 204, pp. 270-288.
Europe, Spain
REE
Abstract: Gran Canaria is a hotspot-derived, intraplate, oceanic island, comprising a variety of alkaline felsic magmatic rocks (i.e. phonolites, trachytes, rhyolites and syenites). These rocks are enriched in rare-earth elements (REE) in relation to the mean concentration in the Earth's crust and they are subsequently mobilised and redistributed in the soil profile. From a set of 57 samples of felsic rocks and 12 samples from three paleosol profiles, we assess the concentration and mobility of REE. In the saprolite that developed over the rhyolites, we identified REE-bearing minerals such as primary monazite-(Ce), as well as secondary phases associated with the edaphic weathering, such as rhabdophane-(Ce) and LREE oxides. The averaged concentration of REE in the alkaline bedrock varies from trachytes (449?mg?kg?1), to rhyolites (588?mg?kg?1) and to phonolites (1036?mg?kg?1). REE are slightly enriched in saprolites developed on trachyte (498?mg?kg?1), rhyolite (601?mg?kg?1) and phonolite (1171?mg?kg?1) bedrocks. However, B-horizons of paleosols from trachytes and phonolites showed REE depletion (436 and 994?mg?kg?1, respectively), whereas a marked enrichment was found in soils developed on rhyolites (1584?mg?kg?1). According to our results, REE resources on Gran Canaria are significant, especially in Miocene alkaline felsic magmatic rocks (declining stage) and their associated paleosols. We estimate a total material volume of approximately 1000?km3 with REE concentrations of 672?±?296?mg?kg?1, yttrium contents of 57?±?30?mg?kg?1, and light and heavy REE ratios (LREE/HREE) of 17?±?6. This mineralisation can be considered as bulk tonnage and low-grade ore REE deposits but it remains necessary to develop detailed mineral exploration on selected insular zones in the future, without undermining environmental and socioeconomic interests.
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.
Abstract: Rock quantity and age are fundamental features of Earth's crust that pertain to many problems in geoscience. Here we combine new estimates of igneous rock area in continental crust from the Macrostrat database (https://macrostrat.org/) with a compilation of detrital zircon ages in order to investigate rock cycling and crustal growth. We find that there is little or no decrease in igneous rock area with increasing rock age. Instead, igneous rock area in North America exhibits four distinct Precambrian peaks, remains low through the Neoproterozoic, and then increases only modestly toward the recent. Peaks in Precambrian detrital zircon age frequency distributions align broadly with peaks in igneous rock area, regardless of grain depositional age. However, detrital zircon ages do underrepresent a Neoarchean peak in igneous rock area; young grains and ca. 1.1 Ga grains are also overrepresented relative to igneous area. Together, these results suggest that detrital zircon age distributions contain signatures of continental denudation and sedimentary cycling that are decoupled from the cycling of igneous source rocks. Models of continental crustal evolution that incorporate significant early increase in volume and increased sedimentation in the Phanerozoic are well supported by these data.
The Australian Gemmologist, Vol. 26, 5&6, pp. 88-99.
South America, Brazil, Minas Gerais
deposit - Alto Paranaiba
Abstract: The authors, in a paper in this journal in 2009, note a puzzle, that in spite of extensive exploration for diamonds by major producers in the Alto Paranaiba region of West Minas Gerais State, Brazil, no primary source, such as kimberlites, for the many diamonds produced since their discovery over 250 years has been found. To answer this puzzle we propose that the diamonds are present within a large extrusive volcanic unit probably derived from the Serra Negra alkaline-carbonatitic complex which comprises a super volcano. This origin fits with the 1995 prediction of Nixon on the future direction of diamona-exploration that extrusive units may contain very large volumes of ore, and that carbonatitic emplacement sources need to be considered. The authors argue, based on available evidence from geology and geophysics, that such an origin is compatible with the known data, but that much additional information is needed to substantiate these ideas. Diamonds of the Alto Paraniaba, Brazil: Nixon's prediction verified?
Abstract: The presence and speciation of volatile C-H-O elements in the silicate systems play an important role in the genesis of magmas on the Earth’s mantle, due to the fact that these elements, mainly in the form of H2O, CO2, CH4 and CxHy, decrease the solidi temperatures of source rocks, making magmatism possible in Earth’s present day thermal conditions [1]. Among those elements, carbon is the only element that changes its valence according to the oxygen fugacity (fO2) conditions of the environment, resulting in different speciation, as: CO3 -2, CO2, Cgraphite/diamond, CH4 or heavier hydrocarbons. In the present work, we are determining phase stability of minerals, water, CO2 and CH4 in the system Nefeline-Kalsilite-Diopside. Our experiments are conducted under 4.0 GPa and temperatures up to 1300°C, using a 1000 tonf hydraulic press coupled with toroidal chambers. Preliminary experiments performed at 1300°C and 4.0GPa (initial composition in the Olivine-Quartz- Kalsalite/Nepheline system: 40mol% Ol90, 40mol% Nph50Kls50 and 20mol% Qz, PH2O,CO2=Ptotal) resulted in the formation of forsterite (Fo90) in equilibrium with phlogopite (Phl), melt and volatile phases (CO2 and CH4). Closer to the Diopside vertice, the addition of CO3 to the sample resulted in a imisibility of a carbonatitic and a silicatic melt, in which the carbonititic melt is enriched in sodium, while the silcate melt is enriched in potassium. Appart from that, experiments in different parts of the diagram suggest compositions from nephelinite-kalsilitite to lamproites composition for the silicate melt in equilibrium with diopside (solid solution with omphacite) and phlogopite. This work is a continuation of previous work in the anhydrous diagram and future works will provide the addition of CH4 as the volatile phase
Recognition of emplacement time of Jambil carbonatite complex from NW Pakistan: constraints from fission track dating of apatite using age standard approach.
GAC Annual Meeting Halifax May 15-19, Abstract 1p.
