Oxygen isotopic zoning of reversely zoned melilite crystals in a fluffy type A Ca‐Al‐rich inclusions from the Vigarano meteorite

Abstract– The oxygen isotopic microdistributions within melilite measured using in situ secondary ion mass spectrometry correspond to the chemical zoning profiles in single melilite crystals of a fluffy type A Ca‐Al‐rich inclusions (CAIs) of reduced CV3 Vigarano meteorite. The melilite crystals show chemical reverse zoning within an individual single crystal from the åkermanite‐rich core to the åkermanite‐poor rim. The composition changes continuously with the crystal growth. The zoning structures suggest that the melilite grew in a hot nebular gas by condensation with decreasing pressure. The oxygen isotopic composition of melilite also changes continuously from ¹⁶O‐poor to ¹⁶O‐rich with the crystal growth. These observations suggest that the melilite condensation proceeded with change consistent with an astrophysical setting around the inner edge of a protoplanetary disk where both ¹⁶O‐rich solar coronal gas and ¹⁶O‐poor dense protoplanetary disk gas could coexist. Fluffy type A CAIs could have been formed around the inner edge of the protoplanetary disk surrounding the early sun.     

The Kaidun meteorite: Composition and origin of inclusions in the metal of an enstatite chondrite clast

Abstract— Metal nodules are one of the major textural components of Kaidun sample #01.3.06 EH3-4. In terms of structure, the nodules are of three types: (1) globular, (2) zoned with a massive core and globular mantle, and (3) nodules with no internal structure. The size and composition of the globules in the nodules and grains of metal of the matrix are almost identical: no greater than 20 μm and Ni, 5.95; Si, 3.33 wt%. The nodules contain small (usually <5 μm) inclusions of SiO₂; albitic glass; enstatite; roedderite; and a mixture of SiO₂ and Na₂S₂. This is the first reported occurrence of a simple sulfide of an alkaline metal in nature. The formation of the inclusions appears to be related to condensation of material onto the surfaces of metal grains. The nodules appear to have formed by aggregation of separate grains (globules) of metal, with conservation of condensates on the grain surfaces as inclusions. The inclusions probably condensed over a significant temperature range from 1400 to 600 K. The aggregation of metal grains and formation of the nodules probably occurred simultaneously with condensation.     

LA‐ICP‐MS Pb isotope test of meteorite provenance: A terrestrial origin for Lovina

Lovina, classified as an ungrouped ataxite, is controversial and its identity as a meteorite has been questioned. In this work, we use Pb isotopes on targeted troilite nodules in Lovina as a test of its antiquity and provenance. Although precise ages cannot be obtained, LA‐ICP‐MS offers a rapid, straightforward procedure to establish the source of lead, whether ancient (meteoritic) or modern (terrestrial). For nine pristine, unweathered nodules in Lovina, we find a lead isotopic composition of: ²⁰⁶Pb/²⁰⁸Pb = 0.492 ± 0.003 (2σ, MSWD 0.79; 95%) and ²⁰⁷Pb/²⁰⁶Pb = 0.852 ± 0.003 (2σ, MSWD 1.09; 95%) with no detectable uranium. All lead compositions of the troilite fall in the range expected for modern environmental and mantle lead and are distinctly different from the primordial Canyon Diablo Troilite (CDT) composition of ancient meteoritic troilite. Although the origin of Lovina remains unknown, we conclude that lead in the Lovina troilite is unsupported by U decay and originated from a terrestrial source.     

Carbon isotopic fractionation in Fischer‐Tropsch‐type reactions and relevance to meteorite organics

Abstract— Fischer‐Tropsch‐type (FTT) reactions have been hypothesized to contribute to the formation of organic compounds in the early solar system, but it has been difficult to identify a signature of such reactions in meteoritic organics. The work reported here examined whether temperature‐dependent carbon isotopic fractionation of FTT reactions might provide such a signature. Analyses of bulk organic deposits resulting from FTT experiments show a slight trend toward lighter carbon isotopic ratios with increasing temperature. It is unlikely, however, that these carbon isotopic signatures could provide definitive provenance for organic compounds in solar system materials produced through FTT reactions, because of the small scale of the observed fractionations and the possibility that signatures from many different temperatures may be present in any specific grain.     

Ni/S/Cl systematics and the origin of impact‐melt glasses in Martian meteorite Elephant Moraine 79001

Martian meteorite Elephant Moraine A79001 (EET 79001) has received considerable attention for the unusual composition of its shock melt glass, particularly its enrichment in sulfur relative to the host shergottite. It has been hypothesized that Martian regolith was incorporated into the melt or, conversely, that the S‐enrichment stems from preferential melting of sulfide minerals in the host rock during shock. We present results from an electron microprobe study of EET 79001 including robust measurements of major and trace elements in the shock melt glass (S, Cl, Ni, Co, V, and Sc) and minerals in the host rock (Ni, Co, and V). We find that both S and major element abundances can be reconciled with previous hypotheses of regolith incorporation and/or excess sulfide melt. However, trace element characteristics of the shock melt glass, particularly Ni and Cl abundances relative to S, cannot be explained either by the incorporation of regolith or sulfide minerals. We therefore propose an alternative hypothesis whereby, prior to shock melting, portions of EET 79001 experienced acid‐sulfate leaching of the mesostasis, possibly groundmass feldspar, and olivine, producing Al‐sulfates that were later incorporated into the shock melt, which then quenched to glass. Such activity in the Martian near‐surface is supported by observations from the Mars Exploration Rovers and laboratory experiments. Our preimpact alteration model, accompanied by the preferential survival of olivine and excess melting of feldspar during impact, explains the measured trace element abundances better than either the regolith incorporation or excess sulfide melting hypothesis does.     

Associations of organic matter with minerals in Tagish Lake meteorite via high spatial resolution synchrotron‐based FTIR microspectroscopy

We have investigated spatial and spectral associations between mineral species and organic matter in the Tagish Lake meteorite. Synchrotron‐based infrared microspectroscopy allowed us to spatially locate specific organic and inorganic compounds within multiple Tagish Lake grains with high spatial resolution. Generated two‐dimensional infrared maps present strong spatial association between aliphatic C‐H and OH in phyllosilicates in Tagish Lake grains. These observations indicate possible roles of phyllosilicates for the formation, evolution, and preservation of organic matter. Infared spectra of all studied Tagish Lake grains show a strong carbonate band, which also shows a weak but positive correlation with organic matter in some grains. However, intergrain correlation was not observed between carbonates and organics, which is likely due to the difference of carbonate occurrence, e.g., presence of larger grains or intergrowth of carbonates on phyllosilicates. Possible scenarios further explaining the observed associations of organics with phyllosilicates and carbonates are presented.     

Ca‐Al‐Fe‐rich inclusion in the Vigarano CV3 chondrite

Abstract– An anomalous Ca‐Al‐Fe‐rich spherical inclusion (CAFI) was found in the Vigarano CV3 chondrite. The CAFI has an igneous texture and contains large amounts of almost pure and coarse‐grained hercynite grains (approximately 56 vol%) as well as refractory phases such as grossite and perovskite. However, melilite and Mg‐spinel, which are common in ordinary Ca‐Al‐rich inclusions, are very rare (<1 vol%). Another unique characteristic of the CAFI is the presence in its core of dmitryivanovite (CaAl₂O₄), which was formed by shock metamorphism of a low‐pressure form of CaAl₂O₄ that was originally crystallized from a molten droplet. The fine‐grained hercynite and unidentified aluminous phase in the rim of the CAFI may have been produced from grossite during aqueous alteration in the Vigarano parent body.     

Transmission electron microscopy of minerals in the martian meteorite Allan Hills 84001

Abstract— We have studied carbonate and associated oxides and glasses in a demountable section of Allan Hills 84001 (ALH 84001) using optical, scanning, and transmission electron microscopy (TEM) to elucidate their origins and the shock history of the rock. Massive, fracture‐zone, and fracture‐filling carbonates in typical locations were characterized by TEM, X‐ray microanalysis, and electron diffraction in a comprehensive study that preserved textural and spatial relationships. Orthopyroxene is highly deformed, fractured, partially comminuted, and essentially unrecovered. Lamellae of diaplectic glass and other features indicate shock pressures >30 GPa. Bridging acicular crystals and foamy glass at contacts of orthopyroxene fragments indicate localized melting and vaporization of orthopyroxene. Carbonate crystals are >5 mm in size, untwinned, and very largely exhibit the R3c calcite structure. Evidence of plastic deformation is generally found mildly only in fracture‐zone and fracture‐filling carbonates, even adjacent to highly deformed orthopyroxene, and appears to have been caused by low‐stress effects including differential shrinkage. High dislocation densities like those observed in moderately shocked calcite are absent. Carbonate contains impactderived glasses of plagioclase, silica, and orthopyroxene composition indicating brief localized impact heating. Stringers and lenses of orthopyroxene glass in fracture‐filling carbonate imply flow of carbonates and crystallization during an impact. Periclase (MgO) occurs in magnesite as 30–50 nm crystals adjacent to voids and negative crystals and as ?1 μm patches of 3 nm crystals showing weak preferred orientation consistent with (111)_MgO//(0001)_carb, as observed in the thermal decomposition of CaCO₃ to CaO. Magnetite crystals that are epitaxially oriented at voids, negative crystals, and microfractures clearly formed in situ. Fully embedded, faceted magnetites are topotactically oriented, in general with (111)_mag//(0001)_carb, so that their oxygen layers are aligned. In optically opaque rims, magnetites are more irregularly shaped and, except for the smallest crystals, poorly aligned. All magnetite and periclase crystals probably formed by exsolution from slightly non‐stoichiometric, CO₂‐poor carbonate following impact‐induced thermal decomposition. Any magnetites that existed in the rock before shock heating could not have preserved evidence for biogenic activity.     

An abiotic origin for hydrocarbons in the Allan Hills 84001 martian meteorite through cooling of magmatic and impact‐generated gases

Abstract— Thermodynamic calculations of metastable equilibria were used to evaluate the potential for abiotic synthesis of aliphatic and polycyclic aromatic hydrocarbons (PAHs) in the martian meteorite Allan Hills (ALH) 84001. The calculations show that PAHs and normal alkanes could form metastably from CO, CO², and H² below approximately 250–300°C during rapid cooling of trapped magmatic or impact‐generated gases. Depending on temperature, bulk composition, and oxidation‐reduction conditions, PAHs and normal alkanes can form simultaneously or separately. Moreover, PAHs can form at lower H/C ratios, higher CO/CO² ratios, and higher temperatures than normal alkanes. Dry conditions with H/C ratios less than approximately 0.01–0.001 together with high CO/CO² ratios also favor the formation of unalkylated PAHs. The observed abundance of PAHs, their low alkylation, and a variable but high aromatic to aliphatic ratio in ALH 84001 all correspond to low H/C and high CO/CO² ratios in magmatic and impact gases and can be used to deduce spatial variations of these ratios. Some hydrocarbons could have been formed from trapped magmatic gases, especially if the cooling was fast enough to prevent reequilibration. We propose that subsequent impact heating(s) in ALH 84001 could have led to dissociation of ferrous carbonates to yield fine‐grain magnetite, formation of a CO‐rich local gas phase, reduction of water vapor to H², reequilibration of the trapped magmatic gases, aromatization of hydrocarbons formed previously, and overprinting of the synthesis from magmatic gases, if any. Rapid cooling and high‐temperature quenching of CO‐, H²‐rich impact gases could have led to magnetite‐catalyzed hydrocarbon synthesis     

Fracture‐related intracrystalline transformation of olivine to ringwoodite in the shocked Sixiangkou meteorite

Abstract— Magnesium‐iron olivine in the Sixiangkou L6 chondrite contains abundant fractures induced by plastic deformation during shock metamorphism. This study reports the discovery of lamellar ringwoodite that incoherently nucleated and grew along planar and irregular fractures in olivine. Magnesium‐iron interdiffusion took place between olivine matrix and crystallizing ringwoodite at high pressures and high temperatures, which resulted in higher FeO content in ringwoodite lamellae than in olivine. This suggests that a quasi‐hydrostatic high pressure lasting for several minutes should have been produced in the shock veins of the meteorite. The intracrystalline transformation of olivine to ringwoodite also has implications for phase transitions in subducting lithospheric slabs because planar and irregular fractures are commonly produced in olivine that suffered plastic deformation.     

Rhenium-187—osmium-187 in iron meteorites and the strange origin of the Kodaïkanal meteorite

Abstract— A set of iron meteorites was investigated for Re-Os isotopes and provides a well-defined isochron age of 4.624 ± 0.017 Ba and an initial ¹⁸⁷Os/¹⁸⁸Os ratio of 0.095636 ± 0.00009. Actual ages may be a few percent lower due to uncertainty on the ¹⁸⁷Re decay constant. Within the small sample number presented here, there is no evidence for age differences between classes. A more detailed study of the meteorite Kodaïkanal shows that the metal reservoir of this meteorite formed approximately at the same time as the other iron meteorites, in contrast with the silicate inclusions which display a formation age of 3.67 Ba with all other chronometers. A collisional origin is in agreement with the data on this meteorite. Major secondary events do not affect the Re-Os system at the bulk rock scale in metal as it is the sole significant reservoir of these two elements. A Re-Os and Rb-Sr investigation of meteoritic troilite exhibits disturbed chronometric systems, which we attribute to the terrestrial history of the meteorite.     

26Al‐26Mg systematics of Ca‐Al‐rich inclusions,amoeboid olivine aggregates,and chondrules from the ungrouped carbonaceous chondrite Acfer 094

Abstract— We report in situ magnesium isotope measurements of 7 porphyritic magnesium‐rich (type I) chondrules, 1 aluminum‐rich chondrule, and 16 refractory inclusions (14 Ca‐Al‐rich inclusions [CAIs] and 2 amoeboid olivine aggregates [AOAs]) from the ungrouped carbonaceous chondrite Acfer 094 using a Cameca IMS 6f ion microprobe. Both AOAs and 9 CAIs show radiogenic ²⁶Mg excesses corresponding to initial ²⁶Al/²⁷Al ratios between ～5 × 10^?5 ～7 × 10^?5 suggesting that formation of the Acfer 094 CAIs may have lasted for ～300,000 years. Four CAIs show no evidence for radiogenic ²⁶Mg; three of these inclusions (a corundum‐rich, a grossite‐rich, and a pyroxene‐hibonite spherule CAI) are very refractory objects and show deficits in ²⁶Mg, suggesting that they probably never contained ²⁶Al. The fourth object without evidence for radiogenic ²⁶Mg is an anorthite‐rich, igneous (type C) CAI that could have experienced late‐stage melting that reset its Al‐Mg systematics. Significant excesses in ²⁶Mg were observed in two chondrules. The inferred ²⁶Al/²⁷Al ratios in these two chondrules are (10.3 ± 7.4) × 10^?6 (6.0 ± 3.8) × 10^?6 (errors are 2σ), suggesting formation 1.6^+1.2_‐0.6 and 2.2^+0.4_‐0.3 Myr after CAIs with the canonical ²⁶Al/²⁷Al ratio of 5 × 10^?5. These age differences are consistent with the inferred age differences between CAIs and chondrules in primitive ordinary (LL3.0–LL3.1) and carbonaceous (CO3.0) chondrites.     

Data‐driven taxonomy matching of asteroid and meteorite

The matching of asteroids and meteorites is a significant step toward a better understanding of the origin, structure, and history of the solar system. We propose a data‐driven approach for investigating common taxonomic structure between asteroids and meteorites; C‐, S‐, and V‐type for the former, and carbonaceous chondrite, ordinary chondrite, and howardite‐eucrite‐diogenite (HED) meteorite for the latter. In the numerical experiments, by checking whether the taxonomy information of meteorites improves classification for asteroid data, we examine the existence of common structure over the two domains. For this purpose, we compare the resultant accuracies of two clustering methods which are with/without the guidance of meteorite data. We observe that the guidance of meteorite taxonomy improves the accuracy for classifying asteroids, either with the reflectance spectra or major chemical compositions of meteorites. This fact serves as a piece of evidence that there is a common taxonomic structure and links between meteorites and asteroids, supporting a long‐standing hypothesis.     

Low‐temperature phase decomposition in iron‐nickel metal of the Portales Valley meteorite

Abstract— The Portales Valley meteorite provides an opportunity to investigate and compare the microstructure in Fe‐Ni metal of the metallic particles in the chondritic portion and in the metal veins. The low‐temperature phase decomposition of Fe‐Ni metal was investigated using scanning electron microscopy, transmission electron microscopy, and atomic force microscopy. The microstructure is formed as the Portales Valley meteorite cooled from high temperatures and includes the outer taenite rim, the cloudy zone, clear taenite, and martensite. Martensite in turn decomposes into a fine admixture of fcc rods in a bcc matrix. The width of the island phase of the cloudy zone in the metal particles of the chondritic portion and the metal veins can be used to estimate a low‐temperature cooling rate. The microstructural evidence indicates that the chondritic portions and the metal veins in the Portales Valley meteorite cooled together as a mixture with a cooling rate of roughly 6.5 K/Ma.     

Differentiation and evolution of the IVA meteorite parent body: Clues from pyroxene geochemistry in the Steinbach stony‐iron meteorite

Abstract— We analyzed the Steinbach IVA stony‐iron meteorite using scanning electron microscopy (SEM), electron microprobe analysis (EMPA), laser ablation inductively‐coupled‐plasma mass spectroscopy (LA‐ICP‐MS), and modeling techniques. Different and sometimes adjacent low‐Ca pyroxene grains have distinct compositions and evidently crystallized at different stages in a chemically evolving system prior to the solidification of metal and troilite. Early crystallizing pyroxene shows evidence for disequilibrium and formation under conditions of rapid cooling, producing clinobronzite and type 1 pyroxene rich in troilite and other inclusions. Subsequently, type 2 pyroxene crystallized over an extensive fractionation interval. Steinbach probably formed as a cumulate produced by extensive crystal fractionation (?60–70% fractional crystallization) from a high‐temperature (?1450–1490 °C) silicate‐metallic magma. The inferred composition of the precursor magma is best modeled as having formed by ≥30–50% silicate partial melting of a chondritic protolith. If this protolith was similar to an LL chondrite (as implied by O‐isotopic data), then olivine must have separated from the partial melt, and a substantial amount (?53–56%) of FeO must have been reduced in the silicate magma. A model of simultaneous endogenic heating and collisional disruption appears best able to explain the data for Steinbach and other IVA meteorites. Impact disruption occurred while the parent body was substantially molten, causing liquids to separate from solids and oxygen‐bearing gas to vent to space, leading to a molten metal‐rich body that was smaller than the original parent body and that solidified from the outside in. This model can simultaneously explain the characteristics of both stony‐iron and iron IVA meteorites, including the apparent correlation between metal composition and metallographic cooling rate observed for metal.     

Description of a very dense meteorite collection area in western Atacama: Insight into the long‐term composition of the meteorite flux to Earth

We describe the geological, morphological, and climatic settings of two new meteorite collections from Atacama (Chile). The “El Médano collection” was recovered by systematic on‐foot search in El Médano and Caleta el Cobre dense collection areas and is composed of 213 meteorites before pairing, 142 after pairing. The “private collection” has been recovered by car by three private hunters and consists of 213 meteorites. Similar to other hot desert finds, and contrary to the falls and Antarctica finds, both collections show an overabundance of H chondrites. A recovery density can be calculated only for the El Médano collection and gives 251 and 168 meteorites larger than 10 g km^?2, before and after pairing, respectively. It is by far the densest collection area described in hot deserts. The Atacama Desert is known to have been hyperarid for a long period of time and, based on cosmic‐ray exposure ages on the order of 1–10 Ma, to have been stable over a period of time of several million years. Such a high meteorite concentration might be explained invoking either a yet unclear concentration mechanism (possibly related to downslope creeping) or a previously underestimated meteorite flux in previous studies or an average terrestrial age over 2 Myr. This last hypothesis is supported by the high weathering grade of meteorites and by the common terrestrial fragmentation (with fragments scattered over a few meters) of recovered meteorites.     

Remnants of altered meteorite in the Cretaceous‐Paleogene clay boundary in Poland

Fossil iron meteorites are extremely rare in the geological sedimentary record. The paleometeorite described here is the first such finding at the Cretaceous‐Paleogene (K‐Pg) boundary. In the boundary clay from the outcrop at the Lechówka quarry (Poland), fragments of the paleometeorite were found in the bottom part of the host layer. The fragments of meteorite (2–6 mm in size) and meteoritic dust are metallic‐gray in color and have a total weight of 1.8181 g. Geochemical and petrographic analyses of the meteorite from Lechówka reveal the presence of Ni‐rich minerals with a total Ni amount of 2–3 wt%. The identified minerals are taenite, kamacite, schreibersite, Ni‐rich magnetite, and Ni‐rich goethite. No relicts of silicates or chromites were found. The investigated paleometeorite apparently represents an independent fall and does not seem to be derived from the K‐Pg impactor. The high degree of weathering did not permit the chemical classification of the meteorite fragments. However, the recognized mineral inventory, lack of silicates, and their pseudomorphs and texture may indicate that the meteorite remains were an iron meteorite.     

Compound‐specific carbon isotope compositions of aldehydes and ketones in the Murchison meteorite

Compound‐specific carbon isotope analysis (δ¹³C) of meteoritic organic compounds can be used to elucidate the abiotic chemical reactions involved in their synthesis. The soluble organic content of the Murchison carbonaceous chondrite has been extensively investigated over the years, with a focus on the origins of amino acids and the potential role of Strecker‐cyanohydrin synthesis in the early solar system. Previous δ¹³C investigations have targeted α‐amino acid and α‐hydroxy acid Strecker products and reactant HCN; however, δ¹³C values for meteoritic aldehydes and ketones (Strecker precursors) have not yet been reported. As such, the distribution of aldehydes and ketones in the cosmos and their role in prebiotic reactions have not been fully investigated. Here, we have applied an optimized O‐(2,3,4,5,6‐pentafluorobenzyl)hydroxylamine (PFBHA) derivatization procedure to the extraction, identification, and δ¹³C analysis of carbonyl compounds in the Murchison meteorite. A suite of aldehydes and ketones, dominated by acetaldehyde, propionaldehyde, and acetone, were detected in the sample. δ¹³C values, ranging from ?10.0‰ to +66.4‰, were more ¹³C‐depleted than would be expected for aldehydes and ketones derived from the interstellar medium, based on interstellar ¹²C/¹³C ratios. These relatively ¹³C‐depleted values suggest that chemical processes taking place in asteroid parent bodies (e.g., oxidation of the IOM) may provide a secondary source of aldehydes and ketones in the solar system. Comparisons between δ¹³C compositions of meteoritic aldehydes and ketones and other organic compound classes were used to evaluate potential structural relationships and associated reactions, including Strecker synthesis and alteration‐driven chemical pathways.     

Mid‐infrared study of stones from the Sutter's Mill meteorite

The Sutter's Mill meteorite fell in northern California on April 22, 2012. Several fragments of the meteorite were recovered, some of them shortly after the fall, others several days later after a heavy rainstorm. In this work, we analyzed several samples of four fragments―SM2, SM12, SM20, and SM30―from the Sutter's Mill meteorite with two infrared (IR) microscopes operating in the 4000–650 cm^?1 (2.5–15.4 μm) range. Spectra show absorption features associated with minerals such as olivines, phyllosilicates, carbonates, and possibly pyroxenes, as well as organics. Spectra of specific minerals vary from one particle to another within a given stone, and even within a single particle, indicating a nonuniform mineral composition. Infrared features associated with aliphatic CH₂ and CH₃ groups associated with organics are also seen in several spectra. However, the presence of organics in the samples studied is not clear because these features overlap with carbonate overtone bands. Finally, other samples collected within days after the rainstorm show evidence for bacterial terrestrial contamination, which indicates how quickly meteorites can be contaminated on such small scales.