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The Sheahan Diamond Literature Reference Compilation - Scientific and Media Articles based on Major Keyword - Moissanite
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 announcements called 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 Keyword Index
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
Each article reference in the SDLRC is tagged with one or more key words assigned by Pat Sheahan to highlight the main topics of the article. In an effort to make it easier for users to track down articles related to a specific topic, KRO has extracted these key words and developed a list of major key words presented in this Key Word Index to which individual key words used in the article reference have been assigned. In most of the individual Key Word Reports the references are in crhonological order, though in some such as Deposits the order is first by key word and then chronological. Only articles classified as "technical" (mainly scientific journal articles) and "media" (independent media articles) are included in the Key Word Index. References that were added in the most recent monthly update are highlighted in yellow.
Moissanite is the name given to natural silicon carbide which has been found in meteor impact craters and some kimberlites and lamproites. It has also been found as inclusions within diamonds. Because natural silicon carbide is very rare, all applications use synthetic silicon carbide. Because of its optical properties and hardness just below diamond synthetic moissanite has been marketed as an alternative to diamond.
Abstract: Hundred-micrometer-sized calcium-aluminum-silicates (CAS) inclusions occur in moissanite-4H, moissanite-15R, and moissanite-6H from Turkey. These inclusions commonly consist of tabular exsolution lamellae of two different minerals. By combined electron microprobe and Raman spectroscopy analysis, at least eight different, essentially Mg- and Fe-free Ca-Al-silicate or Al-silicate phases have been discerned. The most common phase is dmisteinbergite, a hexagonal modification of CaAl2Si2O8, occurring in association with lamellae of Cax(Al,Si)1?xO3 or Ca1?x(Al,Si)2+xO5 compositions. All three phases contain significant amounts of BaO (up to 2 mol% of celsiane component in dmisteinbergite), SrO, SO3, and light rare earth elements (LREE). In particular, Ca1?x(Al,Si)2+xO5 contains up to 2.1 wt% of LREE, 3.9 wt% of F, and significant traces of Cl, while it is also associated to osbornite (TiN). Pure ghelenite, Ca2Al2SiO7, and three additional compositions, namely CaAl4-xSixO7, Ca1-x(Al,Si)3+xO6, and Ca3-x(Al,Si)6+xO14 have been found, either occurring as single grains or forming exsolution lamellae. They also contain significant amounts of BaO, SrO, SO3, and LREE. One last intriguing phase is composed in average of 65.9 wt% SiO2, 17.4% Al2O3, 3.0% alkalis, 6.0% BaO, 2.0% CaO+MgO, 0.9% ZrO2, and up to 0.5% LREE. Dmisteinbergite and ghelenite show Raman peaks in very good agreement with literature data, Cax(Al,Si)1-xO3 shows main Raman modes at 416 and 1009 cm?1, Ca1-x(Al,Si)3+xO6 at 531 and 1579 cm?1 while Ca3-x(Al,Si)6+xO14 has a strong peak at 553 cm?1. CaAl4-xSixO7 shows a weak Raman pattern, while Ca1-x(Al,Si)2+xO5 has no detectable Raman modes. Since the association moissanite-CAS is thermodynamically not stable at ambient pressure and moissanite crystals hosting the CAS phases have ?13C values typical of deep-mantle origin, we interpret the CAS inclusions as partially retrogressed HP minerals. Striking analogies exist between observed CAS compositions and experimentally obtained HP-HT mineralogy. For instance, Cax(Al,Si)1-xO3 contains up to 25 mol% of Al2O3, which is considered as the upper limit of alumina solubility in Ca-perovskite. The study confirms that CAS phases are an important mantle depository for large ion lithophile elements (LILE) and LREE.
Abstract: This ending talk, focused on the ongoing cooperative research of Prof. Griffin and his team at Macquarie University and Shefa Yamim, since January 2014, highlighting unique corundum species characteristics. Preliminary results of this research were presented in the IGS Annual Meeting of 2015, whereas this year Prof. Griffin has shared innovative findings only microscopically tracked within titanium-rich corundum aggregates. One of the more abundant minerals is Tistarite (Ti2O3), previously known only as a single grain in a primitive type of meteorite (!). An article has been submitted to a scientific journal detailing this first terrestrial occurrence. Several other minerals are common in meteorites, but unknown or extremely rare on Earth. About half of these minerals are unknown to science, and will be described as new minerals in the scientific literature. The first of these is a Titanium-Aluminium-Zirconium oxide, informally known as TAZ; it will be submitted to the International Mineralogical Association for recognition as a new mineral, ShefaTAZite. Using state of the art technologies such as Thermal Ionisation Mass Spectrometry (TIMS) and Electron Microscopy Facility (EMF) that has three scanning electron microscopes, all with EBSD capability, and a transmission electron microscope - Prof. Griffin revealed spectacular imagery of minerals and rare compounds associated with titanium rich corundum aggregates.
Geological Society of America Annual Meeting, Vol. 47, 7, p. 163. abstract
Europe, Turkey
Moissanite
Abstract: The Aladag ophiolite in the eastern Tauride belt, southern Turkey, is a well-preserved remnant of oceanic lithosphere. It consists of, in ascending order, harzburgitic to dunitic tectonites, ultramafic and mafic cumulates, isotropic gabbros, sheeted dikes and basaltic pillow lavas. Podiform chromitites are common in the mantle peridotites. Thus far, more than 200 grains of microdiamond and more than 100 grains of moissanite (SiC) have been separated from one sample of podiform chromitite. The microdiamonds occur mostly as subhedral to euhedral, colorless to pale yellow grains, about 50-300 ?m in size. Moissanite grains are generally subhedral, light blue to deep blue in color and variable in size. These grains of diamond and moissanite are very similar to in-situ grains in podiform chromitites of Tibet and the Polar Urals of Russia (Yang et al., 2014; 2015), indicating that they are natural minerals, not the result of natural or anthropogenic contamination. As reported elsewhere, the diamonds and moissanite are accompanied by a range of other minerals, including rutile, zircon, quartz and sulfides. The discovery of diamond, moissanite and other unusual minerals in the podiform chromitites of the Aladag massif provide additional evidence for the widespread occurrence of these minerals in ophiolites, indicating that they are related to global mantle processes.
Abstract: The minimum oxygen fugacity (fO2) of Earth's upper mantle probably is controlled by metal saturation, as defined by the iron-wüstite (IW) buffer reaction (FeO ? Fe + O). However, the widespread occurrence of moissanite (SiC) in kimberlites, and a suite of super-reduced minerals (SiC, alloys, native elements) in peridotites in Tibet and the Polar Urals (Russia), suggest that more reducing conditions (fO2 = 6-8 log units below IW) must occur locally in the mantle. We describe pockets of melt trapped in aggregates of corundum crystals ejected from Cretaceous volcanoes in northern Israel which contain high-temperature mineral assemblages requiring extremely low fO2 (IW < -10). One abundant phase is tistarite (Ti2O3), previously known as a single grain in the Allende carbonaceous chondrite (Mexico) and believed to have formed during the early evolution of the solar nebula. It is associated with other reduced phases usually found in meteorites. The development of super-reducing conditions in Earth's upper mantle may reflect the introduction of CH4 + H2 fluids from the deep mantle, specifically related to deep-seated volcanic plumbing systems at plate boundaries.
Abstract: Here, we present studies of natural SiC that occurs in situ in tuff related to the Miocene alkaline basalt formation deposited in northern part of Israel. Raman spectroscopy, SEM and FIB-assisted TEM studies revealed that SiC is primarily hexagonal polytypes 4H-SiC and 6H-SiC, and that the 4H-SiC polytype is the predominant phase. Both SiC polytypes contain crystalline inclusions of silicon (Sio) and inclusions of metal-silicide with varying compositions (e.g. Si58V25Ti12Cr3Fe2, Si41Fe24Ti20Ni7V5Zr3, and Si43Fe40Ni17). The silicides crystal structure parameters match Si2TiV5 (Pm-3 m space group, cubic), FeSi2Ti (Pbam space group, orthorhombic), and FeSi2 (Cmca space group, orthorhombic) respectively. We hypothesize that SiC was formed in a local ultra-reduced environment at respectively shallow depths (60-100 km), through a “desilification” reaction of SiO2 with highly reducing fluids (H2O-CH4-H2-C2H6) arisen from the mantle “hot spot” and passing through alkaline basalt magma reservoir. SiO2 (melt) interacting with the fluids may originate from the walls of the crustal rocks surrounding this magmatic reservoir. The “desilification” process led to the formation of SiC and the reduction of metal-oxides to native metals, alloys, and silicides. The latter were trapped by SiC during its growth. Hence, interplate “hot spot” alkali basalt volcanism can now be included as a geological environment where SiC, silicon, and silicides can be found.
Abstract: Moissanite (SiC) occurs in mantle and mantle-generated rocks from different tectonic settings. SiC is stable only at low oxygen fugacity (ƒO2) ?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.
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.
Abstract: The Cameca 1280-HR large geometry SIMS instrument is a highly versatile analytical tool which can support a broad range of geochemical applications. Research using the Potsdam 1280 instrument focuses primarily on isotope ratio determinations in geomaterials. Optimized measurement protocols have already been established for ?18O determinations in zircon, and we are also working towards routine oxygen isotope determinations for quartz, calcite, mica, apatite and titanite. The primary challenge in developing such measurement systems are the identification and characterization of suitable reference materials (RMs), and this is made particularly challenging due to the matrix dependent ion yields of the SIMS ion source. Here we wish to report our progress towards establishing new analytical protocols for the determination of ?13C in both diamond and moissanite. In the case of diamond, our facility possesses three natural RMs with which we are able to produce data with a typical analytical repeatability of ?0.15 ‰ (1sd). An inter-comparison of our three diamond RMs demonstrates an overall data quality of better than 0.5‰ in terms of systematic offset between the various materials characterized using gas source mass spectrometry (Palot et al., 2012). A single such ?13C determination in diamond requires 80 s of data acquisition and involves a test portion mass of ?400 pg of material. In-house diamond reference materials for ?15N calibration allow us to measure this isotopic system to a total analytical uncertainty of ± 1.6 ‰ (1sd) at nitrogen concentrations reaching down to 250 ?g/g. Due to the relatively low abundance of nitrogen in diamonds, such isotope ratio determinations require around 9 minutes of data collection. With respect to ?13C determinations in moissanite, we use a kimberlitic SiC as calibrant (Mathez et al., 1995), on which we achieve a repeatability of ?0.2 ‰ (1sd) on a ?350 pg test portion mass. Total data acquisition time for such measurements is 80 s. We are currently in the process of developing a second moissanite RM based on a synthetic, coarse-grained powder. We will also investigate this new material for its ?30Si characteristics.
Abstract: In recent years diamonds and other unusual minerals (carbides, nitrides, metal alloys and native elements) have been recovered from mantle peridotites and chromitites (both high-Cr chromitites and high-Al chromitites) from a number of ophiolites of different ages and tectonic settings. Here we report a similar assemblage of minerals from the Skenderbeu massif of the Mirdita zone ophiolite, west Albania. So far, more than 20 grains of microdiamonds and 30 grains of moissanites (SiC) have been separated from the podiform chromitite. The diamonds are mostly light yellow, transparent, euhedral crystals, 200-300 ?m across, with a range of morphologies; some are octahedral and cuboctahedron and others are elongate and irregular. Secondary electron images show that some grains have well-developed striations. All the diamond grains have been analyzed and yielded typical Raman spectra with a shift at ?1325 cm?1. The moissanite grains recovered from the Skenderbeu chromitites are mainly light blue to dark blue, but some are yellow to light yellow. All the analyzed grains have typical Raman spectra with shifts at 766 cm?1, 787 cm?1, and 967 cm?1. The energy spectrums of the moissanites confirm that the grains are composed entirely of silicon and carbon. This investigation expands the occurrence of diamonds and moissanites to Mesozoic ophiolites in the Neo-Tethys. Our new findings suggest that diamonds and moissanites are present, and probably ubiquitous in the oceanic mantle and can provide new perspectives and avenues for research on the origin of ophiolites and podiform chromitites.
Abstract: Here, we present studies of natural SiC that occurs in situ in tuff related to the Miocene alkaline basalt formation deposited in northern part of Israel. Raman spectroscopy, SEM and FIB-assisted TEM studies revealed that SiC is primarily hexagonal polytypes 4H-SiC and 6H-SiC, and that the 4H-SiC polytype is the predominant phase. Both SiC polytypes contain crystalline inclusions of silicon (Sio) and inclusions of metal-silicide with varying compositions (e.g. Si58V25Ti12Cr3Fe2, Si41Fe24Ti20Ni7V5Zr3, and Si43Fe40Ni17). The silicides crystal structure parameters match Si2TiV5 (Pm-3 m space group, cubic), FeSi2Ti (Pbam space group, orthorhombic), and FeSi2 (Cmca space group, orthorhombic) respectively. We hypothesize that SiC was formed in a local ultra-reduced environment at respectively shallow depths (60-100 km), through a "desilification" reaction of SiO2 with highly reducing fluids (H2O-CH4-H2-C2H6) arisen from the mantle "hot spot" and passing through alkaline basalt magma reservoir. SiO2 (melt) interacting with the fluids may originate from the walls of the crustal rocks surrounding this magmatic reservoir. The "desilification" process led to the formation of SiC and the reduction of metal-oxides to native metals, alloys, and silicides. The latter were trapped by SiC during its growth. Hence, interplate "hot spot" alkali basalt volcanism can now be included as a geological environment where SiC, silicon, and silicides can be found.
Griffin, W.L., Huang, J-X., Thomassot, E., Gain, S.E.M., Toledo, V., O'Reilly, S.Y.
Super-reducing conditions in ancient and modern volcanic systems: sources and behaviour of carbon-rich fluids in the lithospheric mantle ( Mt. Carmel).
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0575-x 14p.
Earth and Planetary Science Letters, Vol. 498, pp. 387-396.
Europe, Bulgaria
moissanite
Abstract: Terrestrial moissanite (SiC) is widely reported as an ultra-high pressure mineral occurring in kimberlites, diamonds and ultramafic/mafic rocks of mantle origin. However, the conditions of crystallization remain largely unknown. Moreover, dozens of SiC occurrences have been reported from continental crust sources such as granitoids, andesite-dacite volcanic rocks and their breccia, metasomatic and metamorphic rocks, and even limestones. The validity of many of these reports is still debated primarily due to possible contaminations from the widespread use of synthetic SiC abrasives in samples preparation. Indeed, reports of well-documented in-situ occurrences of moissanite in association with co-existing minerals are still scarce. The only condition of moissanite formation that is agreed upon is that extremely reducing media are required (e.g. 4.5-6 log units below the iron-wustite buffer). Here, we report the new occurrence of moissanite that was found in-situ within the garnet-staurolite-mica schists of Topolovgrad metamorphic group of Triassic age in Southern Bulgaria. The 10-300 ?m moissanite crystals are situated within 0.1-1.2 mm isolated clusters, filled with amorphous carbon and nanocrystalline graphite. Most of moissanite crystals are 15R (rhombohedral) and 6H (hexagonal) polytypes, and one prismatic crystal, found within them, exhibits unusual concentric polytypical zoning with core (15R), intermediate zone (6H) and rim (3C-cubic). Experimental data show that this type of polytypical zonation is likely due to a decrease in temperature (or/and pressure?) and changes in Si/C ratio. Indeed, amphibolite facies metamorphism (500-580?°C - garnet-staurolite zone) followed by a subsequent cooling during the retrograde stage of green schist facies metamorphism (?400-500?°C) could have provided a change in temperature. The SiC containing clusters exhibit evidence that they are pre-metamorphic, and we hypothesize that their protolith was a "lack shale" material likely rich in carbon, hydrocarbon and terrigenous silica. The latter served as a source of isolated chemically-reduced media, which is required for SiC formation. Other concepts to explain moissanite occurrences in metasedimentary rocks are also discussed. Importantly, our findings show that the formation conditions of moissanite are likely more variable than previously recognized.
Abstract: Silicon carbide (SiC, moissanite) is a common industrial material that is rarely found in terrestrial rocks and meteorites. It has been found to adopt over 300 different crystal structures, most of which are polytypic: they consist of alternating layers of Si and C, with only small stacking faults or shears distinguishing them from one another. In nature, only a few polytypes of SiC have been found, primarily a cubic zincblende type (3C-SiC), several hexagonal wurtzite types (4H-SiC and 6H-SiC), and a rhombohedral type (15R-SiC). Our natural silicon carbide sample is from a Miocene tuff (Yizre’el Valley, Israel) related to interplate alkaline basalt volcanism. Three SiC grains with native silicon and metal silicide inclusions were analyzed using Raman spectroscopy and synchrotron Laue X-ray microdiffraction accompanied by mapping at a 5-8 um resolution. SiC is found to crystallize in only the 4H and 6H polytypes. Due to the crystal orientation of the grains, as well as the significant difference in the c-axis length (~10 vs. ~15 um in 4H and 6H respectively), we were able to unambiguously assign polytypes to each diffraction pattern. Each grain contains large areas where one polytype dominates as a single crystal. In some cases, multiple stacking faults and misoriented polycrystalline aggregates of SiC occur at the 4H/6H interface. In other cases we see intercalation of the 4H and 6H crystals throughout the diffracting volume without a significant change in their crystallographic axes orientation, pointing to a possibly incommensurate crystal structure. Stress and strain are also mapped for all three grains, showing a slight (< 2 ppt) compressive strain in the y direction of all three grains, and a tensile strain in the x and z directions. In the SiC-2 grain, a mostly single-crystalline Si inclusion was found, with an exposed surface diameter of ~30 um. We examine residual strain in Si by both Laue X-ray diffraction and Raman spectroscopy, and find results to generally agree between the two measurements.
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.
Abstract: Moissanites were found in tagamites of the Popigai meteorite crater along with impact diamonds. We have studied 55 samples including 49 individual polytypes and six intergrowths. The numbers of 6H, 15R, 4H, 6H/15R, and 6H/4H polytypes are 82, 7, 5, 4, and 2%, respectively. By the assemblage of polytypes, the moissanites of the Popigai astrobleme are distinct from kimberlite moissanites, as well as from synthetic SiC, which is characterized by the absence of the 4H polytype and the presence of more diverse inclusions (including Fe-bearing). The Popigai astrobleme is one of few objects with reliable natural moissanite. Technogenic contamination is excluded, since any researcher can find this mineral in tagamites.
Abstract: Our discovery of moissanite grains in a peralkaline syenite from the Água de Pau Volcano (São Miguel, Azores Islands, Portugal) represents the first report of this mineral in present day oceanic geodynamic settings. Raman spectroscopy and single-crystal X-ray diffraction show the presence of both the 6H and 4H polytypes with the predominance of the first one. The distribution of trace elements is homogeneous, except for Al and V. Azorean moissanite often hosts rounded inclusions of metallic Si and other not yet identified metallic alloys. A process involving a flushing of CH4-H2 ultra-reducing fluids in the alkaline melts might be considered as a possible mechanism leading to the formation of natural SiC, thus calling for strongly reducing conditions that were locally met in the crust-mantle beneath the São Miguel Island.
Abstract: Our discovery of moissanite grains in a peralkaline syenite from the Água de Pau Volcano (São Miguel, Azores Islands, Portugal) represents the first report of this mineral in present day oceanic geodynamic settings. Raman spectroscopy and single-crystal X-ray diffraction show the presence of both the 6H and 4H polytypes with the predominance of the first one. The distribution of trace elements is homogeneous, except for Al and V. Azorean moissanite often hosts rounded inclusions of metallic Si and other not yet identified metallic alloys. A process involving a flushing of CH4-H2 ultra-reducing fluids in the alkaline melts might be considered as a possible mechanism leading to the formation of natural SiC, thus calling for strongly reducing conditions that were locally met in the crust-mantle beneath the São Miguel Island.
Abstract: Moissanite, SiC, is an uncommon accessory mineral that forms under low oxygen fugacity. Here, we analyze natural SiC from a Miocene tuff-sandstone using synchrotron Laue microdiffraction and Raman spectroscopy, in order to better understand the SiC phases and formation physics. The studied crystals of SiC consist of 4H- and 6H-SiC domains, formed from either, continuous growth or, in one case, intergrown, together with native Si. The native Si is polycrystalline, with a large crystal size relative to the analytical beam dimensions (>1-2 ?m). We find that the intergrown region shows low distortion or dislocation density in SiC, but these features are comparatively high in Si. The distortion/deformation observed in Si may have been caused by a mismatch in the coefficients of thermal expansion of the two materials. Raman spectroscopic measurements are discussed in combination with our Laue microdiffraction results. Our results suggest that these SiC grains likely grew from an igneous melt.
Abstract: The Neoproterozoic Bou Azzer ophiolite in the Moroccan Anti-Atlas Panafrican belt hosts numerous chromitite orebodies within the peridotite section of the oceanic mantle. The chromitites are strongly affected by serpentinization and metamorphism, although they still preserve igneous relicts amenable for petrogenetic interpretation. The major, minor and trace element composition of unaltered chromite cores reveal two compositional groups: intermediate-Cr (Cr# = 0.60 - 0.74) and high-Cr (Cr# = 0.79 - 0.84) and estimates of parental melt compositions suggest crystallization from pulses of fore-arc basalts (FAB) and boninitic melts, respectively, that infiltrated the oceanic supra-subduction zone (SSZ) mantle. A platinum group elements (PGE) mineralization dominated by Ir-Ru-Os is recognized in the chromitites, which has its mineralogical expression in abundant inclusions of Os-Ir alloys and coexisting magmatic laurite (RuS2) and their products of metamorphic alteration. Unusual mineral phases in chromite, not previously reported in this ophiolite, include super-reduced and/or nominally ultra-high pressure minerals moissanite (SiC), native Cu and silicates (oriented clinopyroxene lamellae), but “exotic” zircon and diaspore have also been identified. We interpret that clinopyroxene lamellae have a magmatic origin, whereas super-reduced phases originated during serpentinization processes and diaspore is linked to late circulation of low-silica fluids related to rodingitization. Zircon grains, on the other hand, with apatite and serpentine inclusions, could either have formed after the interaction of chromitite with mantle-derived melts or could represent subducted detrital sediments later incorporated into the chromitites. We offer a comparison of the Bou Azzer chromitites with other Precambrian ophiolitic chromitites worldwide, which are rather scarce in the geological record. The studied chromitites are very similar to the Neoproterozoic chromitites reported in the Arabian-Nubian shield, which are also related to the Panafrican orogeny. Thus, we conclude that the Bou Azzer chromitites formed in a subduction-initiation geodynamic setting with two-stages of evolution, with formation of FAB-derived intermediate-Cr chromitites in the early stage and formation of boninite-derived high-Cr chromitites in the late stage.