Ferrous silicate spherules with euhedral iron‐nickel metal grains from CH carbonaceous chondrites: Evidence for supercooling and condensation under oxidizing conditions

Abstract— The CH carbonaceous chondrites contain a population of ferrous (Fe/(Fe + Mg) ? 0.1‐0.4) silicate spherules (chondrules), about 15–30 μm in apparent diameter, composed of cryptocrystalline olivinepyroxene normative material, ±SiO₂‐rich glass, and rounded‐to‐euhedral Fe, Ni metal grains. The silicate portions of the spherules are highly depleted in refractory lithophile elements (CaO, Al₂O₃, and TiO₂ <0.04 wt%) and enriched in FeO, MnO, Cr₂O₃, and Na₂O relative to the dominant, volatile‐poor, magnesian chondrules from CH chondrites. The Fe/(Fe + Mg) ratio in the silicate portions of the spherules is positively correlated with Fe concentration in metal grains, which suggests that this correlation is not due to oxidation, reduction, or both of iron (FeO_sil ? Fe_met) during melting of metal‐silicate solid precursors. Rather, we suggest that this is a condensation signature of the precursors formed under oxidizing conditions. Each metal grain is compositionally uniform, but there are significant intergrain compositional variations: about 8–18 wt% Ni, <0.09 wt% Cr, and a sub‐solar Co/Ni ratio. The precursor materials of these spherules were thus characterized by extreme elemental fractionations, which have not been observed in chondritic materials before. Particularly striking is the fractionation of Ni and Co in the rounded‐to‐euhedral metal grains, which has resulted in a Co/Ni ratio significantly below solar. The liquidus temperatures of the euhedral Fe, Ni metal grains are lower than those of the coexisting ferrous silicates, and we infer that the former crystallized in supercooled silicate melts. The metal grains are compositionally metastable; they are not decomposed into taenite and kamacite, which suggests fast postcrystallization cooling at temperatures below 970 K and lack of subsequent prolonged thermal metamorphism at temperatures above 400–500 K.     

Compositional variations among whole-rock fragments of the L6 chondrite Bruderheim

Abstract— Twenty ～100-mg random fragments of the Bruderheim chondrite were analyzed by INAA to determine extents of heterogeneity and to check earlier results that gave anomalous LREE concentrations. Considerable compositional heterogeneity was observed in both concentrations (maximum/minimum of 1.7 for Ir, 1.8 for Na, 6.8 for La, 7.4 for Co) and concentration ratios (>3 × for Ni/Co and La/Eu). Compositions could be modelled quantitatively in terms of end-member components of constant composition representing the minerals olivine + orthopyroxene, clinopyroxene, plagioclase, kamacite, taenite, troilite, chromite, and phosphate. The model yields the proportions of minerals in each sample as well as the meteorite as a whole; accurate determination of the end members depends on high intrasample precision for many elements. No evidence of compositional heterogeneity of end members for trace elements was found. It is shown that these analyses, which used only ～2 grams of the meteorite, are equivalent in accuracy to a single sample of several tens of grams, and that knowledge of the extent of heterogeneity is essential to knowing the quality of sampling as well as for comparing results from one analysis with another and of one meteorite with another.     

RARE EARTH AND OTHER ABUNDANCES IN THE MURCHISON CARBONACEOUS METEORITE

The abundances of 27 elements are reported for the Murchison meteorite. Nine of these elements (Al, Ca, Fe, Mn, Na, K, Cr, Co, and Sc) have been determined previously for different Murchison specimens. Abundances for 18 elements (In, Cd, V, Y, and REE) are new data for this meteorite. The chemical composition is similar to the type II carbonaceous chondrites, particularly on the basis of REE, Mn, and In abundances.     

Element mobility due to weathering in the L5 Bayard chondrite

Abstract— In order to assess weathering effects, sixteen elements were determined by neutron activation in the surficial layer and the interior of the extensively weathered Bayard L5 chondrite. Na, As, Sb, La and Sm show enrichment in the surface; for these elements soil concentrations are greater than in the meteorite. Elements showing no significant differences between surface and interior are Sc, Cr, Fe, Co, Ni, Zn, Se, Eu, Yb, Ir and Au; with the exception of Eu and Yb, soil concentrations were lower than those in the chondrite. Concentrations of Fe, Ni and Co, and to some extent Na, are lower than the mean of the L-chondrite values probably due to oxidation and leaching from the chondrite. The data support an L classification for the Bayard chondrite.     

Meteorites from the Lut Desert (Iran)

We present for the first time a detailed report on the discovery of a new meteorite collection region in the Lut Desert, eastern–southeastern Iran, describing its geological, morphological, and climatic setting. Our search campaigns, alongside with the activity of meteorite hunters, yielded >200 meteorite finds. Here, we report on their classification, spatial distribution, and terrestrial weathering. All the collected meteorites are ordinary chondrites (OCs). The most abundant by far are the highly weathered paired H5 distributed in the northwest of Kalut area (central Lut, Kerman dense collection area). The second are well‐preserved paired L5 also found in Kalut region. A detailed study of the geochemistry and mineralogy of selected meteorites reveals significant effects of terrestrial weathering. Fe,Ni metal (hereafter simply metal) and troilite are transformed into Fe oxyhydroxides. A rather unusual type of troilite weathering to pyrite/marcasite is observed in most of the Lut Desert meteorites. Magnetic measurements and X‐ray diffractometry confirm the occurrence of terrestrial weathering products, with the dominance of maghemite, goethite, and hematite. Mobile elements, such as Li, Sr, Mo, Ba, Tl, Th, and U, are enriched with respect to fresh falls. Meanwhile, a decrease in the V, Cr, Co, Rb (and possibly Fe) due to terrestrial weathering is detectable. The total carbon and CaCO₃ is higher than in samples from other hot deserts. The weathering effects observed in the Lut Desert OCs can be used as distinctive indicators to distinguish them from meteorites from other regions of the Earth. Measurements of terrestrial age (¹⁴C) show a range of 10–30 ka, which is in the range of ages reported for meteorites from other hot deserts except the Atacama Desert (Chile). Considering the high potential of the Lut Desert in meteorite preservation, systematic works should lead to the discovery of more samples giving access to interesting material for future studies.     

Mineralogy,petrography, geochemistry,and classification of the Košice meteorite

The Ko?ice meteorite was observed to fall on 28 February 2010 at 23:25 UT near the city of Ko?ice in eastern Slovakia and its mineralogy, petrology, and geochemistry are described. The characteristic features of the meteorite fragments are fan‐like, mosaic, lamellar, and granular chondrules, which were up to 1.2 mm in diameter. The fusion crust has a black‐gray color with a thickness up to 0.6 mm. The matrix of the meteorite is formed mainly by forsterite (Fo_80.6); diopside; enstatite (Fs_16.7); albite; troilite; Fe‐Ni metals such as iron and taenite; and some augite, chlorapatite, merrillite, chromite, and tetrataenite. Plagioclase‐like glass was also identified. Relative uniform chemical composition of basic silicates, partially brecciated textures, as well as skeletal taenite crystals into troilite veinlets suggest monomict breccia formed at conditions of rapid cooling. The Ko?ice meteorite is classified as ordinary chondrite of the H5 type which has been slightly weathered, and only short veinlets of Fe hydroxides are present. The textural relationships indicate an S3 degree of shock metamorphism and W0 weathering grade. Some fragments of the meteorite Ko?ice are formed by monomict breccia of the petrological type H5. On the basis of REE content, we suggest the Ko?ice chondrite is probably from the same parent body as H5 chondrite Morávka from Czech Republic. Electron‐microprobe analysis (EMPA) with focused and defocused electron beam, whole‐rock analysis (WRA), inductively coupled plasma mass and optical emission spectroscopy (ICP MS, ICP OES), and calibration‐free laser induced breakdown spectroscopy (CF‐LIBS) were used to characterize the Ko?ice fragments. The results provide further evidence that whole‐rock analysis gives the most accurate analyses, but this method is completely destructive. Two other proposed methods are partially destructive (EMPA) or nondestructive (CF‐LIBS), but only major and minor elements can be evaluated due to the significantly lower sample consumption.     

Origin of kamacite,schreibersite, and perryite in metal‐sulfide nodules of the enstatite chondrite Sahara 97072 (EH3)

Abstract– Perryite [(Fe,Ni)_x(Si,P)_y], schreibersite [(Fe,Ni)₃P], and kamacite (αFeNi) are constituent minerals of the metal‐sulfide nodules in the Sahara 97072 (EH3) enstatite chondrite meteorite. We have measured concentrations of Ni, Cu, Ga, Au, Ir, Ru, and Pd in these minerals with laser ablation, inductively coupled plasma mass spectrometry (ICP‐MS). We also measured their Fe, Ni, P, Si, and Co concentrations with electron microprobe. In kamacite, ratios of Ru/Ir, Pd/Ir, and Pd/Ru cluster around their respective CI values and all elements analyzed plot near the intersection of the equilibrium condensation trajectory versus Ni and the respective CI ratios. In schreibersite, the Pd/Ru ratio is near the CI value and perryite contains significant Cu, Ga, and Pd. We propose that schreibersite and perryite formed separately near the condensation temperatures of P and Si in a reduced gas and were incorporated into Fe‐Ni alloy. Upon further cooling, sulfidation of Fe in kamacite resulted in the formation of additional perryite at the sulfide interface. Still later, transient heating re‐melted this perryite near the Fe‐FeS eutectic temperature during partial melting of the metal‐sulfide nodules. The metal‐sulfide nodules are pre‐accretionary objects that retain CI ratios of most siderophile elements, although they have experienced transient heating events.     

Buddha from space—An ancient object of art made of a Chinga iron meteorite fragment*

Abstract– The fall of meteorites has been interpreted as divine messages by multitudinous cultures since prehistoric times, and meteorites are still adored as heavenly bodies. Stony meteorites were used to carve birds and other works of art; jewelry and knifes were produced of meteoritic iron for instance by the Inuit society. We here present an approximately 10.6 kg Buddhist sculpture (the “iron man”) made of an iron meteorite, which represents a particularity in religious art and meteorite science. The specific contents of the crucial main (Fe, Ni, Co) and trace (Cr, Ga, Ge) elements indicate an ataxitic iron meteorite with high Ni contents (approximately 16 wt%) and Co (approximately 0.6 wt%) that was used to produce the artifact. In addition, the platinum group elements (PGEs), as well as the internal PGE ratios, exhibit a meteoritic signature. The geochemical data of the meteorite generally match the element values known from fragments of the Chinga ataxite (ungrouped iron) meteorite strewn field discovered in 1913. The provenance of the meteorite as well as of the piece of art strongly points to the border region of eastern Siberia and Mongolia, accordingly. The sculpture possibly portrays the Buddhist god Vai?ravana and might originate in the Bon culture of the eleventh century. However, the ethnological and art historical details of the “iron man” sculpture, as well as the timing of the sculpturing, currently remain speculative.     

THE ORO GRANDE,NEW MEXICO,CHONDRITE AND ITS LITHIC INCLUSION

The Oro Grande, New Mexico, U.S.A., chondrite was found in 1971. Electron microprobe analyses and microscopic examination show the following mineralogy: olivine (Fa 19.3 mole percent), orthopyroxene (Fs 16.2 mole percent), diopside, feldspar (An 13.6 mole percent), chlorapatite, whitlockite, kamacite, taenite, troilite, chromite, and an iron-bearing terrestrial weathering product. A bulk chemical analysis of the meteorite shows the following results (weight percent): Fe 0.84, Ni 1.46, Co 0.07, FeS 3.62, SiO₂ 34.18, TiO₂ 0.14, Al₂O₃ 1.83, Cr₂O₃ 0.55, Fe₂O₃ 21.25, FeO 9.13, MnO 0.31, MgO 21.52, CaO 1.72, Na₂O 0.70, K₂O 0.08, P₂O₅ 0.25, H₂O+ 2.14, H₂O^- 0.40, C 0.22, Sum 100.41. On the basis of composition and texture, the Oro Grande meteorite is classified as an H5 chondrite. A large lithic fragment (～5 mm long) with a very fine-grained texture different from that of the host meteorite was analyzed for bulk composition using the broad beam of an electron microprobe, and was found to be enriched in Ca, Al, Na, and K, and depleted in Mg and Fe relative to the bulk composition of the host meteorite. Its mineral compositions, however, are very similar to those of the host. It is suggested that the fragment is not a xenolith of a previously undescribed type of achondrite, but is probably an impact-produced partial melt of the host chondrite or a fragment of an unusually large chondrule.     

New insights into the mineralogy and weathering of the Meridiani Planum meteorite,Mars

Meridiani Planum is the first officially recognized meteorite find on the surface of Mars. It was discovered at and named after the landing site of the Mars Exploration Rover Opportunity. Based on its composition, it was classified as a IAB complex iron meteorite. Mössbauer spectra obtained by Opportunity are dominated by kamacite (α‐Fe‐Ni) and exhibit a small contribution of ferric oxide. Several small features in the spectra have been neglected to date. To shed more light on these features, five iron meteorite specimens were investigated as analogs to Meridiani Planum with a laboratory Mössbauer setup. Measurements were performed on (1) their metallic bulk, (2) troilite (FeS) inclusions, (3) cohenite ((Fe,Ni,Co)₃C) and schreibersite ((Fe,Ni)₃P), and (4) corroded rims. In addition to these room‐temperature measurements, a specimen from the Mundrabilla IAB‐ungrouped meteorite was measured at Mars‐equivalent temperatures. Based on these measurements, the features in Meridiani Planum spectra can be explained with the presence of small amounts of schreibersite and/or cohenite and iron oxides. The iron oxides can be attributed to a previously reported coating on Meridiani Planum. Their presence indicates weathering through the interaction of the meteorite with small amounts of water.     

Modification of REE distribution of ordinary chondrites from Atacama (Chile) and Lut (Iran) hot deserts: Insights into the chemical weathering of meteorites

The behavior of rare earth elements (REEs) during hot desert weathering of meteorites is investigated. Ordinary chondrites (OCs) from Atacama (Chile) and Lut (Iran) deserts show different variations in REE composition during this process. Inductively coupled plasma–mass spectrometry (ICP‐MS) data reveal that hot desert OCs tend to show elevated light REE concentrations, relative to OC falls. Chondrites from Atacama are by far the most enriched in REEs and this enrichment is not necessarily related to their degree of weathering. Positive Ce anomaly of fresh chondrites from Atacama and the successive formation of a negative Ce anomaly with the addition of trivalent REEs are similar to the process reported from Antarctic eucrites. In addition to REEs, Sr and Ba also show different concentrations when comparing OCs from different hot deserts. The stability of Atacama surfaces and the associated old terrestrial ages of meteorites from this region give the samples the necessary time to interact with the terrestrial environment and to be chemically modified. Higher REE contents and LREE‐enriched composition are evidence of contamination by terrestrial soil. Despite their low degrees of weathering, special care must be taken into account while working on the REE composition of Atacama meteorites for cosmochemistry applications. In contrast, chondrites from the Lut desert show lower degrees of REE modification, despite significant weathering signed by Sr content. This is explained by the relatively rapid weathering rate of the meteorites occurring in the Lut desert, which hampers the penetration of terrestrial material by forming voluminous Fe oxide/oxyhydroxides shortly after the meteorite fall.     

Weathering of meteorites from Oman: Correlation of chemical and mineralogical weathering proxies with 14C terrestrial ages and the influence of soil chemistry

Abstract— Fifty‐four fragments of ordinary chondrites from 50 finds representing all searched areas in central Oman and all weathering stages were selected to compare the physical, chemical, and mineralogical effect of terrestrial weathering with ¹⁴C terrestrial ages. ¹⁴C ages range from 2.0 to >49 kyr with a median value of 17.9 kyr. The peak of the age range, which is between 10–20 kyr, falls in an arid climate period. A comparison of the chemical composition of Omani chondrites with literature data for unweathered H and L chondrites demonstrates a strong enrichment in Sr and Ba, and depletion in S during weathering. Water contents in H chondrites increase with terrestrial age, whereas L chondrites show a rapid initial increase followed by nearly constant water content. Correlating Sr, Ba, and H₂O with age indicates two absorption trends: i) an initial alteration within the first 20 kyr dominated by H₂O uptake, mainly reflecting Fe‐Ni metal alteration, and ii) a second Ba‐and Sr‐dominated stage correlated with slower and less systematic weathering of troilite that starts after H₂O reaches ?2 wt%. Sulfur released from troilite partly combines with Ba and Sr to form sulfate minerals. Other parameters correlated with ¹⁴C age are degree of weathering, color of powdered meteorites, and the Ni/Fe ratio. Chemical analyses of 145 soils show a high degree of homogeneity over the entire interior Oman Desert, indicating large‐scale mixing by wind. Soil samples collected from beneath meteorite finds typically are enriched in Ni and Co, confirming mobilization from the meteorites. High Cr and Ni concentrations in reference soil samples, which decrease from NE to SW, are due to detrital material from ultramafic rocks of the Oman Mountains.     

The formation of rims on calcium‐aluminum‐rich inclusions: Step I—Flash heating

Abstract— Wark‐Lovering rims of six calcium‐aluminum‐rich inclusions (CAIs) representing the main CAI types and groups in Allende, Efremovka and Vigarano were microsurgically separated and analysed by neutron activation analysis (NAA). All the rims have similar ～4x enrichments, relative to the interiors, of highly refractory lithophile and siderophile elements. The NAA results are confirmed by ion microprobe and scanning electron microscope (SEM) analyses of rim perovskites and rim metal grains. Less refractory Eu, Yb, V, Sr, Ca and Ni are less enriched in the rims. The refractory element patterns in the rims parallel the patterns in the outer parts of the CAIs. In particular, the rims on type B1 CAIs have the igneously fractionated rare earth element (REE) pattern of the melilite mantle below the rim and not the REE pattern of the bulk CAI, proving that the refractory elements in the rims were derived from the outer mantle and were not condensates onto the CAIs. The refractory elements were enriched in an Al₂O₃‐rich residue <50 μm thick after the most volatile ～80% of the outermost 200 μm of each CAI had been volatilized, including much Mg, Si and Ca. Some volatilization occurred below the rim, and created refractory partial melts that crystallized hibonite and gehlenitic melilite. The required “flash heating” probably exceeded 2000 °C, but for only a few seconds, in order to melt only the outer CAI and to unselectively volatilize slow‐diffusing O isotopes which show no mass fractionation in the rim. The volatilization did, however, produce “heavy” mass‐fractionated Mg in rims. In some CAIs this was later obscured when “normal” Mg diffused in from accreted olivine grains at relatively high temperature (not the lower temperature meteorite metamorphism) and created the ～50 μm set of monomineralic rim layers of pyroxene, melilite and spinel.     

Silica‐rich igneous rims around magnesian chondrules in CR carbonaceous chondrites: Evidence for condensation origin from fractionated nebular gas

Abstract— The outer portions of many type I chondrules (Fa and Fs <5 mol%) in CR chondrites (except Renazzo and Al Rais) consist of silica‐rich igneous rims (SIRs). The host chondrules are often layered and have a porphyritic core surrounded by a coarse‐grained igneous rim rich in low‐Ca pyroxene. The SIRs are sulfide‐free and consist of igneously‐zoned low‐Ca and high‐Ca pyroxenes, glassy mesostasis, Fe, Ni‐metal nodules, and a nearly pure SiO₂ phase. The high‐Ca pyroxenes in these rims are enriched in Cr (up to 3.5 wt% Cr₂O₃) and Mn (up to 4.4 wt% MnO) and depleted in Al and Ti relative to those in the host chondrules, and contain detectable Na (up to 0.2 wt% Na₂O). Mesostases show systematic compositional variations: Si, Na, K, and Mn contents increase, whereas Ca, Mg, Al, and Cr contents decrease from chondrule core, through pyroxene‐rich igneous rim (PIR), and to SIR; FeO content remains nearly constant. Glass melt inclusions in olivine phenocrysts in the chondrule cores have high Ca and Al, and low Si, with Na, K, and Mn contents that are below electron microprobe detection limits. Fe, Ni‐metal grains in SIRs are depleted in Ni and Co relative to those in the host chondrules. The presence of sulfide‐free, SIRs around sulfide‐free type I chondrules in CR chondrites may indicate that these chondrules formed at high (>800 K) ambient nebular temperatures and escaped remelting at lower ambient temperatures. We suggest that these rims formed either by gas‐solid condensation of silica‐normative materials onto chondrule surfaces and subsequent incomplete melting, or by direct SiO_(gas) condensation into chondrule melts. In either case, the condensation occurred from a fractionated, nebular gas enriched in Si, Na, K, Mn, and Cr relative to Mg. The fractionation of these lithophile elements could be due to isolation (in the chondrules) of the higher temperature condensates from reaction with the nebular gas or to evaporation‐recondensation of these elements during chondrule formation. These mechanisms and the observed increase in pyroxene/olivine ratio toward the peripheries of most type I chondrules in CR, CV, and ordinary chondrites may explain the origin of olivine‐rich and pyroxene‐rich chondrules in general.     

Chemical compositions of impact melt breccias and target rocks from the Tenoumer impact crater,Mauritania

Abstract— The impact melt breccias from the Tenoumer crater (consisting of a fine‐grained intergrowth of plagioclase laths, pyroxene crystals, oxides, and glass) display a wide range of porosity and contain a large amount of target rock clasts. Analyses of major elements in impact melt rocks show lower contents of SiO₂, Al₂O₃, and Na₂O, and higher contents of MgO, Fe₂O₃, and CaO, than the felsic rocks (i.e., granites and gneisses) of the basement. In comparison with the bulk analyses of the impact melt, the glass is strongly enriched in Si‐Al, whereas it is depleted both in Mg and Fe; moreover, the impact melt rocks are variably enriched or depleted in some REE with respect to the felsic and mafic bedrock types. Gold is slightly enriched in the impact melt, and Co, Cr, and Ni abundances are possibly due to a contribution from mafic bedrock. Evidences of silicate‐carbonate liquid immiscibility, mainly as spherules and globules of calcite within the silicate glass, have been highlighted. HMX mixing calculation confirm that the impact melt rocks are derived from a mixing of at least six different target lithologies outcropping in the area of the crater. A large contribution is derived from granitoids (50%) and mica schist (17–19%), although amphibolites (?15%), cherty limestones (?10%), and ultrabasites (?6%) components are also present. The very low abundances of PGE in the melt rock seem to come mainly from some ultrabasic target rocks; therefore, the contamination from the meteoritic projectile appears to have been negligible.     

Magnesian anorthositic granulites in lunar meteorites Allan Hills A81005 and Dhofar 309: Geochemistry and global significance

Abstract– Fragments of magnesian anorthositic granulite are found in the lunar highlands meteorites Allan Hills (ALH) A81005 and Dhofar (Dho) 309. Five analyzed clasts of meteoritic magnesian anorthositic granulite have Mg′ [molar Mg/(Mg + Fe)] = 81–87; FeO ≈ 5% wt; Al₂O₃ ≈ 22% wt; rare earth elements abundances ≈ 0.5–2 × CI (except Eu ≈ 10 × CI); and low Ni and Co in a non‐chondritic ratio. The clasts have nearly identical chemical compositions, even though their host meteorites formed at different places on the Moon. These magnesian anorthositic granulites are distinct from other highlands materials in their unique combination of mineral proportions, Mg′, REE abundances and patterns, Ti/Sm ratio, and Sc/Sm ratio. Their Mg′ is too high for a close relationship to ferroan anorthosites, or to have formed as flotation cumulates from the lunar magma ocean. Compositions of these magnesian anorthositic granulites cannot be modeled as mixtures of, or fractionates from, known lunar rocks. However, compositions of lunar highlands meteorites can be represented as mixtures of magnesian anorthositic granulite, ferroan anorthosite, mare basalt, and KREEP. Meteoritic magnesian anorthositic granulite is a good candidate for the magnesian highlands component inferred from Apollo highland impactites: magnesian, feldspathic, and REE‐poor. Bulk compositions of meteorite magnesian anorthositic granulites are comparable to those inferred for parts of the lunar farside (the Feldspathic Highlands Terrane): ～4.5 wt% FeO; ～28 wt% Al₂O₃; and Th <1 ppm. Thus, magnesian anorthositic granulite may be a widespread and abundant component of the lunar highlands.     

THE LOOP CHONDRITE: PETROLOGY,MINERAL CHEMISTRY,AND OPAQUE MINERALOGY

The Loop meteorite was found in 1962 in Gaines County, Texas, at a location very close to that where the Ashmore chondrite was found in 1969. The two specimens were assumed to be fragments of the same meteorite. The Loop meteorite is a type L6 chondrite composed of olivine (Fo_75.4Fa_24.6), orthopyroxene (En_77.6Wo_1.5Fs_20.9), clinopyroxene (En_47.5Wo_45.1Fs_7.4), plagioclase (Ab_84.3Or_5.5An_10.2), Fe-Ni metal, troilite, and chromite. Fe-Ni metal is represented by kamacite (5.8-6.4 wt % Ni, 0.88-1.00 wt % Co), taenite (30.0–52.9 wt % Ni, 0.16-0.34 wt % Co), and plessite (16.8–28.5 wt % Ni, 0.38-0.54 wt % Co). Native copper occurs as rare inclusions in Fe-Ni metal. Both chondrules and matrix have similar mineral compositions. The mineral chemistry of the Loop meteorite is quite different from that of the Ashmore, which was classified as an H5 chondrite by Bryan and Kullerud (1975). Therefore, the Ashmore and Loop meteorites are two different chondrites, even though they were recovered from the same geographic location.     

Petrogenesis of basaltic shergottite Northwest Africa 5298: Closed‐system crystallization of an oxidized mafic melt

Abstract– Northwest Africa (NWA) 5298 is an evolved basaltic shergottite that has bulk characteristics and mineral compositions consistent with derivation from an oxidized reservoir in Mars. Chemically zoned clinopyroxene (64.5%, augite and pigeonite), with interstitial lath‐shaped plagioclase (29.4%, An₄₀ to An₅₅), constitutes the bulk of this meteorite. The plagioclase has been converted by shock to both isotropic maskelynite and spherulitic, birefringent feldspar representing a quenched vesicular melt. The remainder of the rock consists of minor amounts of Fe‐Ti oxides (ilmenite and titanomagnetite), phosphates (merrillite and apatite), silica polymorph, fayalite, pyrrhotite, baddeleyite, and minor hot desert weathering products (calcite and barite). Oxygen fugacity derived from Fe‐Ti oxide thermobarometry is close to the quartz‐fayalite‐magnetite (QFM) buffer indicating that the late stage evolution of this magma occurred under more oxidizing condition than those recorded in most other shergottites. Merrillite contains the largest abundances of rare earth elements (REE) of all phases, thereby controlling the REE budget in NWA 5298. The calculated bulk rock REE pattern normalized to CI chondrite is relatively flat. The evolution of the normalized REE patterns of the bulk rock, clinopyroxene, plagioclase, and phosphate in NWA 5298 is consistent with closed‐system chemical behavior with no evidence of crustal contamination or postcrystallization disturbance of the REE contents of these phases.     

Characterization of iron meteorites by scanning electron microscopy,x-ray diffraction,magnetization measurements,and Mössbauer spectroscopy: Mundrabilla IAB-ung

A fragment of Mundrabilla IAB-ung iron meteorite was analyzed using optical microscopy, scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), magnetization measurements, and Mössbauer spectroscopy. The polished section of meteorite fragment characterization by optical microscopy and SEM shows the presence of the γ-Fe(Ni, Co) phase lamellae, plessite structures and schreibersite inclusions in the α-Fe(Ni, Co) phase. EDS indicates variations in the Ni concentrations in the following ranges: (i) ∼6.3–6.5 atom% in the α-Fe(Ni, Co) phase and (ii) ∼22 to ∼45 atom% in the γ-Fe(Ni, Co) phase lamellae including the range of ∼29–33 atom% of Ni leading to the paramagnetic state of the γ-Fe(Ni, Co) phase. Schreibersite inclusions contain ∼23 atom% of P, ∼33 atom% of Fe, ∼43 atom% of Ni, and ∼0.7 atom% of Co. Plessite structure contains the average Ni concentration of ∼17 atom% while detailed EDS analysis shows: (i) the lowest Ni concentrations of ∼5 to ∼8 atom%, (ii) the intermediate Ni concentrations of ∼9 to ∼19 atom%, and (iii) the highest Ni concentration up ∼38 atom% (some individual micro-grains demonstrate up to ∼47 and ∼59 atom% of Ni) that may indicate the presence of the (i) α-Fe(Ni, Co), (ii) α₂-Fe(Ni, Co), and (iii) γ-Fe(Ni, Co) phases. These may be a result of the γ-phase decomposition with mechanism γ → α + α₂ + γ that indicates a slow cooling rate for Mundrabilla IAB-ung iron meteorite. The presence of ∼98.6 wt% of the α-Fe(Ni, Co) phase and ∼1.4 wt% of the γ-Fe(Ni, Co) phase is found by XRD while schreibersite is not detected. Magnetization measurements show the saturation magnetization moment of Mundrabilla IAB-ung of 188(2) emu g⁻¹ indicating a low average Ni concentration in Fe-Ni-Co alloy. Mössbauer spectrum of the bulk Mundrabilla powder demonstrates five magnetic sextets related to the ferromagnetic α₂-Fe(Ni, Co), α-Fe(Ni, Co), and γ-Fe(Ni, Co) phases and one singlet associated with the paramagnetic γ-Fe(Ni, Co) phase, however, there are no spectral components corresponding to schreibersite. Basing on relatively larger and smaller values of the magnetic hyperfine field, two magnetic sextets associated with γ-Fe(Ni, Co) phase can be related to the disordered and more ordered γ-phases. The iron fractions in the detected phases can be roughly estimated as follows: (i) ∼17.6% in the α₂-Fe(Ni, Co) phase, (ii) ∼68.5% in the α-Fe(Ni, Co) phase, (iii) ∼11.5% in the disordered γ-Fe(Ni, Co) phase, (iv) ∼2.0% in the more ordered γ-Fe(Ni, Co) phase, and (v) ∼0.4% in the paramagnetic γ-Fe(Ni, Co) phase.     

THE MINERALOGY AND CHEMISTRY OF THE ALTA'AMEEM METEORITE

The Alta'ameem hypersthene chondrite is a light gray brecciated and metamorphosed meteorite composed mainly of olivine (27% Fa), orthopyroxene (24.5% Fs) and plagioclase (An¹⁰). Other minerals include troilite, kamacite, taenite, chromite, ilmenite, clinopyroxene, chalcopyrite, and apatite or merrillite. The mineralogical and chemical analyses suggest that the Alta'ameem meteorite belongs to the amphoterite group of chondrites. The chemical composition includes the following: Fe 3.39, Ni 1.13, Co 0.05, Cu 0.01, FeS 6.48, SiO₂ 39.48, TiO₂ 0.28, Al₂O₃ 2.25, FeO 16.46, MnO 0.40, MgO 25.66, CaO 1.47, Na₂O 1.05, K₂O 0.15, P₂O₅ 0.47, Cr₂O₃ 0.45; total 99.18.