Nitrogen microanalysis of glass inclusions in chondritic olivines by nuclear reaction

Measured were the abundance and distribution of nitrogen in glasses of glass inclusions in olivines of CV3, CO3, CR, C4, CH3, and LL chondritic meteorites by means of the ¹⁴N(d, p)¹⁵N nuclear reaction. Similar to what was observed with carbon, nitrogen is present in low concentrations (<20 ppm) in the structure of olivines but can by stored in variable amounts in glasses of glass inclusions. These primitive glasses, characterized by a Si-Al-Ca-rich composition, have highly variable nitrogen contents (30 to 1500 ppm) and highly inhomogeneous nitrogen distribution. Nitrogen contents are independent of the chemical composition of the glasses. The heterogeneous distribution is a common feature of all studied inclusions, as is evidenced by the variable contents of nitrogen in glass inclusions occurring in the same olivine grain. Nitrogen heterogeneity is suggestive of trapping of solid nitrogen carrier phases during formation of the constituents of chondrules. However, part of the originally trapped nitrogen appears to have been lost, possibly, by ulterior oxidation and subsequent transformation into volatile species.     

Platinum-group-mineral inclusions in chromite from the bird river sill,Manitoba

Platinum-group minerals (PGM) have been identified as inclusions in chromite from the Bird River Sill, Manitoba. The inclusions are small (<20 microns) and are commonly euhedral. The PGM inclusions are (Ru, Os, Ir) S₂, laurite, and (Os, Ir, Ru alloy), rutheniridosmine: Laurites contain up to 2.99 wt. % palladium. Arsenic content is negligible and no platinum or rhodium has been detected. One platinum-group element alloy contains 0.96 wt. % rhodium but neither platinum nor palladium has been detected. Laurite inclusions in chromite from the ultramafic zone record two compositional trends; first increasing and then decreasing Ru/(Ru+Os+Ir) up section. PGM inclusions and other solid inclusions occur as discrete phases in chromite and are part of the chromite precipitation event. Increasing oxygen fugacity by wall rock assimilation or new magma injection initiates chromite precipitation, locally increasing the sulphur content of the magma to convert PGE alloys to sulphides.     

Uranium in the silicate inclusions of stony-iron and iron meteorites

The microdistribution of U has been studied, using fission track techniques, in eleven mesosiderites, seven pallasites and four iron meteorites with silicate inclusions. When concentrated, U is usually found in phosphates: merrillite and/or chlorapatite. As in stony meteorites, the U concentrations in a given phosphate phase are highly variable from meteorite to meteorite and sometimes also exhibit variations in the same meteorite. Uranium is found to be concentrated in merrillite (0.25 to 1.43 ppm) in all the mesosiderites except Bondoc where none was observed. No U-rich phase was identified in six of the seven pallasites. In the seventh, Marjalahti, there are merrillite grains with concentrations ranging from 0.06 to 0.14 ppm. Where observed, the phosphates from silicate inclusions in the irons appear to have U concentrations similar to the mesosiderites.     

Mineralogy and petrology of silicate inclusions in iron meteorites

Silicate inclusions in 17 iron meteorites have been analyzed by the electron microprobe and classified, according to their phase assemblages, compositions, and textures, into three major types: Odessa, Copiapo, and Weekeroo Station, and three miscellaneous types: Enon, Kendall County, and Netschaëvo. Phase compositions in both Odessa- and Copiapo-type inclusions are very similar, but the two types are different in texture and constituent phases. Weekeroo Station-type inclusions are very different in every respect from other inclusions.For Odessa- and Copiapo-type inclusions, the distribution coefficients of Fe²⁺ and Mg in coexisting orthopyroxene and clinopyroxene indicate equilibration temperatures of 1,000° C, and the Ca/(Ca+Mg) ratios indicate temperatures of 900° C to 1,000° C. Equilibration temperatures determined for chromite-olivine pairs have a higher range of 1,154° C to 1,335° C. Minor element distributions among coexisting ferromagnesian silicates in these inclusions follow consistent patterns and are constant for any given sample, suggesting equilibrium assemblages. Major and minor element distributions for Weekeroo Station inclusions are anomalous, indicating nonequilibrium.Compositional data, the fragmentary shapes of many inclusions, the highly differentiated characteristic of two types of inclusions, the apparent disequilibrium between kamacite in inclusions and kamacite of the iron host, and the relict chondrules found in Netschaëvo suggest that many of the inclusions did not form cogenetically with the iron host, but represent pre-existing stony material that was taken up by an iron melt, probably not in the core of the parent body (or bodies).     

Foreign inclusions in stony meteorites—I. Carbonaceous chondritic xenoliths in the Kapoeta howardite

Small, 1–3 millimeter-sized, black xenoliths containing chondrules and chondrule fragments embedded in a fine-grained matrix are present in the Kapoeta howardite. Forsteritic olivine, pentlandite and a nickel-rich (0.3–2.8 wt. %) matrix indicate that these xenoliths are carbonaceous ohondrite material.     

Fluid inclusions in chromite from a pyroxenite dike of the Pindos ophiolite complex

Chromitite occurrences in the Pindos ophiolite complex are located in elongated dunite bodies hosted in harzburgite of the mantle sequence, and show a compositional variation from high-Al to high-Cr type. Although the majority of the chromite ores is characterized by paucity in fluid inclusions, abundant fluid inclusions were found in chromite hosted by a coarse-grained pyroxenite dike at the Spanos Valley, Pindos complex. Chromite occurs in highly variable proportion in an orthopyroxene matrix or as inclusions in orthopyroxenes. Its composition is homogeneous and has an average Cr/(Cr+Al) ratio 0.73.The investigation of chromitites revealed the presence of primary and secondary fluid inclusions. The primary inclusions are of following types: Three-phase solid-liquid-gas, three-phase liquid-liquid-gas, two-phase liquid-gas and one-phase octahedron crystal-shaped. The secondary fluid inclusions are two-phase liquid-gas and mono-phase fluid inclusions.The presence of fluid inclusions in chromite aggregates hosted in orthopyroxenite dikes, in combination with the trace element contents in chromite concentrates and the mineralogical composition of the dikes may indicate that an aqueous phase separated from the magma.     

Mineralogy of silicate inclusions in the Elga IIE iron meteorite

The petrography, mineral modal data and major and trace element compositions of 15 silicate inclusions in the Elga iron meteorite (chemical group IIE) show that these inclusions represent chemically homogeneous zoned objects with highly variable structures, reflecting the sequence of crystallization of a silicate melt during cooling of the metal host. The outer zones of inclusions at the interface with their metal host have a relatively medium-grained hypocrystalline texture formed mainly by Cr-diopside and merrillite crystals embedded in high-silica glass, whereas the central zones have a fine-grained hypocrystalline texture. Merrillite appears first on the liquidus in the outer zones of the silicate inclusions. Na and REE concentrations in merrillite from the outer zones of inclusions suggest that it may have crystallized as α-merrillite in the temperature range of 1300–1700°С. Merrillite tends to preferentially accumulate Eu without Sr. Therefore, strongly fractionated REE patterns are not associated with prolonged differentiation of the silicate melt source but depend on crystallization conditions of Н-chondrite droplets in a metallic matrix. The systematic decrease in Mg# with increasing Fe/Mn in bronzite may indicate partial reduction of iron during crystallization of the inclusion melt. The modal and bulk compositions of silicate inclusions in the Elga meteorite, as well as the chemical composition of phases are consistent with the model equilibrium crystallization of a melt, corresponding to 25% partial melting of H-chondrite, and the crystallizing liquidus phase, merrillite, and subsequent quenching at about 1090°С. Despite a high alkali content of the average weighted bulk inclusion composition, La/Hf and Rb/Th fall within the field of H chondrites, suggesting their common source. Our results reveal that silicate inclusions in the Elga (IIE) iron meteorite originated by mixing of two impact melts, ordinary chondrite and Ni-rich iron with а IIE composition, which were produced by impact event under near-surface conditions on a partially differentiated parent asteroid.     

Mineralogy of carbonaceous chondritic microclasts in howardites: identification of C2 fossil micrometeorites

Seventy-one carbonaceous chondritic microclasts of average size 150 μm have been found in three howardites (Yamato-793497, Jodzie, Kapoeta). All carbonaceous chondritic microclasts are made of a fine-grained phyllosilicate-rich matrix supporting a variety of minerals such as olivine, pyroxene, spinel, iron oxides, iron-nickel sulfides, and calcium carbonates. Such a mineralogy is typical of chondritic C2 matter. Half of the carbonaceous chondritic microclasts are tochilinite-rich, and have been tentatively called CM2 microclasts. The other half are magnetite-rich, and have been tentatively called CR2 microclasts. The absence of a correlation between the CM2/CR2 ratio in carbonaceous chondritic microclasts and in numerous millimeter-sized clasts found in the same sections argues for carbonaceous chondritic microclasts being true micrometeorites rather than fragments of larger objects. Dynamical simulations show that it is possible for asteroidal dust to encounter Vesta (the howardite’s putative parent-asteroid) at velocity low enough (<1 km.s⁻¹) to prevent fragmentation. Because the micrometeorite flux in the inner Solar System has been decreasing with time, we argue that carbonaceous chondritic microclasts have been trapped in Vesta’s regolith early in the history of the Solar System and are fossil micrometeorites. Because both microclasts and clasts found in howardites are related to C2 chondritic matter, we propose that C2 matter represents the bulk, or at least a significant fraction of the primordial howardite parent-asteroid. Considering the abundance of C2 matter among fossil micrometeorites, we speculate that the C2 fossil micrometorites are the so far unidentified agent of the late chondritic veneer that endowed the Earth’s mantle with an excess of siderophile elements relative to the contents predicted by the core-mantle separation models. The discovery that C2 fossil micrometeorites are similar to C2 modern Antarctic micrometeorites supports recent models proposing a micrometeoritic origin for the Earth’s oceans and volatile species.     

西藏康金拉铬铁矿床刚玉中的包裹体研究

西藏康金拉铬铁矿石的矿物学研究中,发现大量的微粒金刚石和碳硅石等超高压异常地幔矿物,表明它们产在一个强还原的高压环境.本研究在铬铁矿石中还发现了刚玉及其中大量的矿物包裹体.电子探针等方法研究表明,包裹体的种类包括简单氧化物,如金红石;自然钛;Ti-N、Ti-Si、Ti-C、Ti-Si-P、Ti-B等合金类;含稀土元素的硅酸盐矿物,以及一些未知矿物.结合对铬铁矿石中其他矿物的研究成果,认为康金拉铬铁矿石中的刚玉及其中的强还原环境形成的矿物组合形成于深部地幔.因此,康金拉铬铁矿石中的刚玉可以认为是一种新的带有高压环境信息的标志性矿物.     

矿物包体分类问题及其意义（一种新的包体分类方案）

一、概述包体是矿物形成过程中被捕获的成矿介质,被称为成矿流体的样品。它是矿物最重要的标型特征之一。可作为译解成矿作用,特别是内生成矿作用的密码。因此,包体是一种最好的材料,可用于测定矿物、矿床或其他地质体形成过程中的物理地球化学作用的温度、压力、介质成分及性质等。用这些参数,可以有助于解决有关矿床成因、找矿标志、成矿规律及指     

A composition-independent quantitative determination of the water content in silicate glasses and silicate melt inclusions by confocal Raman spectroscopy

A new approach was developed to measure the water content of silicate glasses using Raman spectroscopy, which is independent of the glass matrix composition and structure. Contrary to previous studies, the compositional range of our studied silicate glasses was not restricted to rhyolites, but included andesitic, basaltic and phonolitic glasses. We used 21 glasses with known water contents for calibration. To reduce the uncertainties caused by the baseline removal and correct for the influence of the glass composition on the spectra, we developed the following strategy: (1) application of a frequency-dependent intensity correction of the Raman spectra; (2) normalization of the water peak using the broad T–O and T–O–T vibration band at 850–1250 cm⁻¹ wavenumbers (instead of the low wavenumber T–O–T broad band, which appeared to be highly sensitive to the FeO content and the degree of polymerization of the melt); (3) normalization of the integrated Si-O band area by the total number of tetrahedral cations and the position of the band maximum. The calibration line shows a ±0.4 wt% uncertainty at one relative standard deviation in the range of 0.8–9.5 wt% water and a wide range of natural melt compositions. This method provides a simple, quick, broadly available and cost-effective way for a quantitative determination of the water content of silicate glasses. Application to silicate melt inclusions yielded data in good agreement with SIMS data.     

Platinum-group minerals and other solid inclusions in chromite of ophiolitic complexes: Occurrence and petrological significance

Summary Platinum-group mineral, silicate and other solid and fluid inclusions occur in disseminated and massive chromite in a variety of lithologies from ophiolitic and other mafic-ultramafic complex-types. The inclusions are small (<250 microns) and randomly distributed throughout their host. Silicate inclusions are modally more abundant than the other inclusion types. Platinum-group mineral phases are ruthenium-rich sulphides and PGE alloys are osmium-rich. Mafic silicates (olivine, pyroxenes, pargasitic-amphiboles, micas) are magnesium-, titanium-, and alkali-rich and felsic silicates are sodium-rich (albite, nepheline).The intimate association of these inclusions with chromite suggests that their origin must be considered within a chromite crystallization model. A hypothesis of origin is suggested wherein the platinum-group minerals and silicates are trapped as discrete, crystalline euhedral phases and silicate liquid during the precipitation of chromite. The similarity of physical characteristics, modal mineralogy and chemical compositions indicates that this model may be applicable to all mafic-ultramafic complex-types.

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Minerale der Platin-Gruppe und andere feste Einschlüsse in Chromiten aus Ophiolit-Komplexen: Vorkommen und petrologische Bedeutung

Zusammenfassung Minerale der Platin-Gruppe, Silikate und andere feste und flüssige Einschlüsse kommen in disseminierten und massiven Chromiten in einer Vielzahl von Gesteinen in ophiolitischen und anderen mafisch-ultramafischen Komplexen vor. Die Einschlüsse sind klein (<250 microns) und unregelmäßig im Chromit verteilt. Silikat-Einschlüsse sind modal weiter verbreitet als andere Arten von Einschlüssen. Minerale der Platin-Gruppe sind durch Ruthenium-reiche Sulfide und Osmium-reiche Legierungen vertreten. Mafische Silikate (Olivin, Pyroxen, pargasitische Amphibole, Glimmer) sind Magnesium-, Titan- und Alkali-reich; felsische Silikate sind Natrium-reich (Albit, Nephelin).Die ausgeprägte Assoziation dieser Einschlüsse mit Chromit weist darauf hin, daß ihre Herkunft im Zusammenhang mit einem Kristallisations-Modell für Chromit zu sehen ist. Ein genetisches Konzept wird vorgelegt, wobei die Platin-Gruppen-Minerale als gut ausgebildete, idiomorphe kristalline Phasen, und die Silikate als Silikatschmelze während des Ausfallens des Chromites eingeschlossen werden. Die Ähnlichkeit der physikalischen Eigenschaften, der modalen mineralogischen Zusammensetzung und der chemischen Zusammensetzung weisen darauf hin, daß dieses Modell auf alle mafisch-ultramafischen Komplexe anzuwenden ist.

     

The compositional classification of chondrites: IV. Ungrouped chondritic meteorites and clasts

Six specimens of unusual chondritic materials were analyzed by neutron activation for 30 elements in order to assess their degree of chondritic compositional pristinity and to search for evidence of genetic links to other chondrites. Five have highly recrystallized textures; the other, the Cumberland Falls chondrite, has suffered minor metamorphic recrystallization. Acapulco and Allan Hills A77081, are closely related and have subpristine compositions; they are more distantly related to Enon which has an altered composition. Udei Station appears to be a IAB meteorite even though its $\text{FeO}\text{(FeO + MgO)}$ ratio is slightly above the IAB field. The highly weathered meteorite Tierra Bianca is closely related to IAB but has a δ¹⁸O value 5 standard deviations higher than the IAB mean and is designated ungrouped. Udei Station and Tierra Bianca have altered compositions; rare earth element patterns indicate loss of a phosphate phase. The elemental composition of the Cumberland Falls chondrite is virtually identical to that of LL chondrites and its O-isotope composition is closely similar to those of some unequilibrated ordinary chondrites including LL Semarkona. The $\text{FeO}\text{(FeO + MgO)}$ ratios in its olivine are generally much lower than those in pyroxene, a relationship we show to be indicative of in situ reduction resulting from exchange with the aubritic host. The names winonaites and forsterite chondrites have no taxonomic utility.     

Relict sand wedges in southern Patagonia and their stratigraphic and paleo-environmental significance

Relict sand wedges are ubiquitous in southern Patagonia. At six sites we conducted detailed investigations of stratigraphy, soils, and wedge frequency and characteristics. Some sections contain four or more buried horizons with casts. The cryogenic features are dominantly relict sand wedges with an average depth, maximum apparent width, minimum apparent width, and H/W of 78, 39, 3.8, and 2.9 cm, respectively. The host materials are fine-textured (silt loam, silty clay loam, clay loam) till and the infillings are aeolian sand. The soils are primarily Calciargidic Argixerolls that bear a legacy of climate change. Whereas the sand wedges formed during very cold (?4 to ?8 °C or colder) and dry (ca. ≤100 mm precipitation/yr) glacial periods, petrocalcic horizons from calcium carbonate contributed by dustfall formed during warmer (7 °C or warmer) and moister (≥250 mm/yr) interglacial periods. The paleo-argillic (Bt) horizons reflect unusually moist interglacial events where the mean annual precipitation may have been 400 mm/yr. Permafrost was nearly continuous in southern Patagonia during the Illinoian glacial stage (ca. 200 ka), the early to mid-Pleistocene (ca. 800–500 ka), and on two occasions during the early Pleistocene (ca. 1.0–1.1 Ma).     

Novel applications of fluid inclusions and isotope geochemistry in unravelling the genesis of fossil travertine systems

The Denizli Basin is a fault‐bounded Neogene–Quaternary depression located in the Western Anatolian Extensional Province, Western Turkey. The basin is a unique geological site with abundant active and fossil (Quaternary) travertine and tufa deposits. Fluid inclusion microthermometry and isotopic analysis were applied to study the genesis of the Ball?k fossil travertine deposits, located in the south‐eastern part of the basin. Microthermometry on fluid inclusions indicates that the main travertine precipitating and cementing fluids are characterized by low salinity (<0·7 wt% NaCl equivalent) and variable temperatures that cluster at <50°C and ca 100°C. Fluids of meteoric origin have been heated by migration to the deeper subsurface, possibly in a local high geothermal gradient setting. A later uncommon cementation phase is related to a fluid with a significantly higher salinity (25·5 to 26·0 wt% bulk). The fluid obtained its salinity by interaction with Late Triassic evaporite layers. Strontium isotopes indicate that the parent carbonate source rock of the different travertine precipitates is very likely to be the Triassic limestone of the Lycian Nappes. Carbon isotopes suggest that the parent CO₂ gas originated from thermal decarbonation of the Lycian limestones with minor contributions of magmatic degassing and organic soil CO₂. Oxygen isotopes confirm the meteoric origin of the fluids and indicate disequilibrium precipitation because of evaporation and degassing. Results were integrated within the available geological data of the Denizli Basin in a generalized travertine precipitation model, which enhanced the understanding of fossil travertine systems. The study highlights the novel application of fluid inclusion research in unravelling the genesis of continental carbonates and provides several recommendations for hydrocarbon exploration in travertine‐bearing sedimentary basins. The findings suggest that travertine bodies and their parent carbonate source rocks have the potential to constitute interesting subsurface hydrocarbon reservoirs.     

The trace element composition of silicate inclusions in diamonds: a review

On a global scale, peridotitic garnet inclusions in diamonds from the subcratonic lithosphere indicate an evolution from strongly sinusoidal REE_N, typical for harzburgitic garnets, to mildly sinusoidal or “normal” patterns (positive slope from LREE_N to MREE_N, fairly flat MREE_N–HREE_N), typical for lherzolitic garnets. Using the Cr-number of garnet as a proxy for the bulk rock major element composition it becomes apparent that strong LREE enrichment in garnet is restricted to highly depleted lithologies, whereas flat or positive LREE–MREE slopes are limited to less depleted rocks. For lherzolitic garnet inclusions, there is a positive relation between equilibration temperature, enrichment in MREE, HREE and other HFSE (Ti, Zr, Y), and decreasing depletion in major elements. For harzburgitic garnets, relations are not linear, but it appears that lherzolite style enrichment in MREE–HREE only occurs at temperatures above 1150–1200 °C, whereas strong enrichment in Sr is absent at these high temperatures. These observations suggest a transition from melt metasomatism (typical for the lherzolitic sources) characterized by fairly unfractionated trace and major element compositions to metasomatism by CHO fluids carrying primarily incompatible trace elements. Melt and fluid metasomatism are viewed as a compositional continuum, with residual CHO fluids resulting from primary silicate or carbonate melts in the course of fractional crystallization and equilibration with lithospheric host rocks.

Eclogitic garnet inclusions show “normal” REE_N patterns, with LREE at about 1× and HREE at about 30× chondritic abundance. Clinopyroxenes approximately mirror the garnet patterns, being enriched in LREE and having chondritic HREE abundances. Positive and negative Eu anomalies are observed for both garnet and clinopyroxene inclusions. Such anomalies are strong evidence for crustal precursors for the eclogitic diamond sources. The trace element composition of an “average eclogitic diamond source” based on garnet and clinopyroxene inclusions is consistent with derivation from former oceanic crust that lost about 10% of a partial melt in the garnet stability field and that subsequently experienced only minor reenrichment in the most incompatible trace elements. Based on individual diamonds, this simplistic picture becomes more complex, with evidence for both strong enrichment and depletion in LREE.

Trace element data for sublithospheric inclusions in diamonds are less abundant. REE in majoritic garnets indicate source compositions that range from being similar to lithospheric eclogitic sources to strongly LREE enriched. Lower mantle sources, assessed based on CaSi–perovskite as the principal host for REE, are not primitive in composition but show moderate to strong LREE enrichment. The bulk rock LREE_N–HREE_N slope cannot be determined from CaSi–perovskites alone, as garnet may be present in these shallow lower mantle sources and then would act as an important host for HREE. Positive and negative Eu anomalies are widespread in CaSi–perovskites and negative anomalies have also been observed for a majoritic garnet and a coexisting clinopyroxene inclusion. This suggests that sublithospheric diamond sources may be linked to old oceanic slabs, possibly because only former crustal rocks can provide the redox gradients necessary for diamond precipitation in an otherwise reduced sublithospheric mantle.     

中国铬铁矿床的再研究及找矿前景

铬铁矿是生产不锈钢不可替代的原材料,中国目前是世界最大不锈钢消费国。铬铁矿一直是中国的短缺矿种,几乎完全依靠进口。铬铁矿床分为层状和豆荚状两种类型矿床。中国已知的铬铁矿床均属于豆荚状铬铁矿床,主要分布在西藏、新疆和内蒙古等地。该类矿床主要产于蛇绿岩型地幔橄榄岩或相关的堆晶杂岩中。最近在西藏罗布莎和俄罗斯乌拉尔豆荚状铬铁矿中发现深部地幔矿物,认为铬铁矿来自深部地幔,不是产自浅部地幔橄榄岩。认为深部来源的铬铁矿可以成大矿,小岩体也可以成大矿,因此,十分有必要对中国境内的蛇绿岩地幔橄榄岩开展新一轮的调查。     

Electron probe microanalysis and microscopy: Principles and applications in characterization of mineral inclusions in chromite from diamond deposit

Electron probe microanalysis and microscopy is a widely used modern analytical technique primarily for quantifying chemical compositions of solid materials and for mapping or imaging elemental distributions or surface morphology of samples at micrometer or nanometer-scale. This technique uses an electromagnetic lens-focused electron beam, generated from an electron gun, to bombard a sample. When the electron beam interacts with the sample, signals such as secondary electron, backscattered electron and characteristic X-ray are generated from the interaction volume. These signals are then examined by detectors to acquire chemical and imaging information of the sample. A unique part of an electron probe is that it is equipped with multiple WDS spectrometers of X-ray and each spectrometer with multiple diffracting crystals in order to analyze multiple elements simultaneously. An electron probe is capable of analyzing almost all elements (from Be to U) with a spatial resolution at or below micrometer scale and a detection limit down to a few ppm.Mineral inclusions in chromite from the Wafangdian kimberlite, Liaoning Province, China were used to demonstrate the applications of electron probe microanalysis and microscopy technique in characterizing minerals associated with ore deposits, specifically, in this paper, minerals associated with diamond deposit. Chemical analysis and SE and BSE imaging show that mineral inclusions in chromite include anhydrous silicates, hydrous silicates, carbonates, and sulfides, occurring as discrete or single mineral inclusions or composite multiple mineral inclusions. The chromite–olivine pair poses a serious problem in analysis of Cr in olivine using electron probe. Secondary fluorescence of Cr in chromite by Fe in olivine drastically increases the apparent Cr₂O₃ content of an olivine inclusion in a chromite. From the chemical compositions obtained using electron probe, formation temperatures and pressures of chromite and its mineral inclusions calculated using applicable geothermobarometers are from 46 kbar and 980 °C to 53 kbar and 1130 °C, which are within the stability field of diamond, thus Cr-rich chromite is a useful indication mineral for exploration of kimberlite and diamond deposit. A composite inclusion in chromite composed of silicate and carbonate minerals has a bulk composition of 33.2 wt.% SiO₂, 2.5 wt.% Al₂O₃, 22.0 wt.% MgO, 7.5 wt.% CaO, 2.5 wt.% BaO, 0.8 wt.% K₂O, 25.5 wt.% CO₂, and 0.8 wt.% H₂O, similar to the chemical composition of the Wafangdian kimberlite, suggesting that it is trapped kimberlitic magma.     

Major, trace element and oxygen isotope study of glass cosmic spherules of chondritic composition: The record of their source material and atmospheric entry heating

New geochemical data on cosmic spherules (187 major element, 76 trace element, and 10 oxygen isotope compositions) and 273 analyses from the literature were used to assess the chemical diversity observed among glass cosmic spherules with chondritic composition. Three chemical groups of glass spherules are identified: normal chondritic spherules, CAT-like spherules (where CAT refers to Ca-Al-Ti-rich spherules), and high Ca-Al spherules. The transition from normal to high Ca-Al spherules occurs through a progressive enrichment in refractory major elements (on average from 2.3 wt.% to 7.0 wt.% for CaO, 2.8 wt.% to 7.2 wt.% for Al₂O₃, and 0.14 wt.% to 0.31 wt.% for TiO₂) and refractory trace elements (from 6.2 μg/g to 19.3 μg/g for Zr and 1.6CI-4.3CI for Rare Earth Elements-REEs) relative to moderately refractory elements (Mg, Si) and volatile elements (Rb, Na, Zn, Pb). Based on a comparison with experimental works from the literature, these chemical groups are thought to record progressive heating and evaporation during atmospheric entry. The evaporative mass losses evaluated for the high Ca-Al group (80-90%) supersede those of the CAT spherules which up to now have been considered as the most heated class of stony cosmic spherules. However, glass cosmic spherules still retain isotopic and elemental evidence of their source and precursor mineralogy. Four out of the 10 normal and high Ca-Al spherules analysed for oxygen isotopes are related to ordinary chondrites (δ¹⁸O = 13.2-17.3‰ and δ¹⁷O = 7.6-9.2‰). They are systematically enriched in Ni and Co (Ni = 24-500 μg/g) with respect to spherules related to carbonaceous chondrites (Ni < 1.2 μg/g, δ¹⁸O = 13.1-28.0‰ and δ¹⁷O = 5.1-14.0‰). REE abundances in cosmic spherules, which are not fractionated according to parent body or atmospheric entry heating, can then be used to unravel the precursor mineralogy. Spherules with flat REE pattern close to unity when normalized to CI are the most abundant in our dataset (54%) and likely derive from homogeneous, fine-grained chondritic precursors. Other REE patterns fall into no more than five categories, a surprising reproducibility in view of the mineralogical heterogeneity of chondritic lithologies at the micrometeorite scale.