Impact glass spherules in the Chicxulub K‐Pg event bed at Beloc,Haiti: Alteration patterns

We have investigated six impact glass spherules from the K‐Pg event bed at Beloc, Haiti, using optical and electron microscopy, electron microprobe and in situ laser ablation–mass spectrometry (LA‐ICP‐MS; 37 trace elements, spot size 90–35 μm), in order to understand geochemical changes during alteration. The mm‐sized glass spherules are partly or totally altered to smectite, but original textural features are preserved. The average trace‐element composition of glass matches that one of the upper continental crust. Hints for a “meteoritic component” are lacking (Ni/Cr < 1.3; Pt below detection limit). Compared to this fresh glass, smectites are strongly depleted in trace elements, except for Li, Sc, V, Ni, Ga, Ge, and Ba. The chondrite‐normalized REE distribution patterns are flat with subchondritic abundances, related to their very low degree of crystallinity. We observe a positive Eu and a strong negative Ce anomaly; the latter is explained by formation of an organic Ce⁴⁺‐complex, soluble under reducing conditions. Zr/Hf of glasses and smectites is chondritic to superchondritic (35–40), whereas Nb/Ta in smectite is subchondritic (5–12) compared to Nb/Ta in the glass (~14–18). The low Nb/Ta is due to the low Nb concentrations in the smectite. Using in situ techniques with high spatial resolution, we have documented for the first time the significant changes in diagnostic elemental ratios during alteration of glass spherules. This has to be taken into account in the interpretation of geochemical data of not only impact materials but also volcanic glass, especially if bulk rock methods are used.     

SIMS studies of Allende projectiles fired into Stardust‐type aluminum foils at 6 km/sec

Abstract— We have explored the feasibility of C, N, and O isotopic measurements by NanoSIMS and of elemental abundance determinations by time‐of‐flight secondary ion mass spectrometry (TOF‐SIMS) on residues of Allende projectiles that impacted Stardust‐type aluminum foils in the laboratory at 6 km/sec. These investigations are part of a consortium study aimed at providing the foundation for the characterization of matter associated with microcraters that were produced during the encounter of the Stardust space probe with comet 81P/Wild‐2. Eleven experimental impact craters were studied by NanoSIMS and eighteen by TOF‐SIMS. Crater sizes were between 3 and 190 μm. The NanoSIMS measurements have shown that the crater morphology has only a minor effect on spatial resolution and on instrumental mass fractionation. The achievable spatial resolution is always better than 200 nm, and C and O isotopic ratios can be measured with a precision of several percent at a scale of several 100 nm, which is the typical size of presolar grains. This clearly demonstrates that presolar matter, provided it survives the impact into the aluminum foil partly intact, is recognizable even if embedded in material of solar system origin. TOF‐SIMS studies are restricted to materials from the crater rim. The element ratios of the major rock‐forming elements in the Allende projectiles are well‐characterized by the TOF‐SIMS measurements, indicating that fractionation of those elements during impact can be expected to be negligible. This permits chemical information on the type of impactor material to be obtained. For any more detailed assignments to specific chondrite groups, however, information on the abundances of the light elements, especially C, is crucial. This information could not be obtained in the present study due to unavoidable contamination during impact experiments.     

Petrography and geochemistry of the enriched basaltic shergottite Northwest Africa 2975

We present a study of the petrology and geochemistry of basaltic shergottite Northwest Africa 2975 (NWA 2975). NWA 2975 is a medium‐grained basalt with subophitic to granular texture. Electron microprobe (EMP) analyses show two distinct pyroxene compositional trends and patchy compositional zoning patterns distinct from those observed in other meteorites such as Shergotty or QUE 94201. As no bulk sample was available to us for whole rock measurements, we characterized the fusion crust and its variability by secondary ion mass spectrometer (SIMS) measurements and laser ablation inductively coupled plasma spectroscopy (LA‐ICP‐MS) analyses as a best‐available proxy for the bulk rock composition. The fusion crust major element composition is comparable to the bulk composition of other enriched basaltic shergottites, placing NWA 2975 within that sample group. The CI‐normalized REE (rare earth element) patterns are flat and also parallel to those of other enriched basaltic shergottites. Merrillite is the major REE carrier and has a flat REE pattern with slight depletion of Eu, parallel to REE patterns of merrillites from other basaltic shergottites. The oxidation state of NWA 2975 calculated from Fe‐Ti oxide pairs is NNO‐1.86, close to the QFM buffer. NWA 2975 represents a sample from the oxidized and enriched shergottite group, and our measurements and constraints on its origin are consistent with the hypothesis of two distinct Martian mantle reservoirs: a reduced, LREE‐depleted reservoir and an oxidized, LREE‐enriched reservoir. Stishovite, possibly seifertite, and dense SiO₂ glass were also identified in the meteorite, allowing us to infer that NWA 2975 experienced a realistic shock pressure of ~30 GPa.     

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.     

Light rare earth element enrichments in ureilites: A detailed ion microprobe study

Abstract— This paper explores the possible origin of the light rare earth element (LREE) enrichments observed in some ureilites, a question that has both petrogenetic and chronologic implications for this group of achondritic meteorites. Rare earth element and other selected elemental abundances were measured in situ in 14 thin sections representing 11 different ureilites. The spatial microdistributions of REEs in C‐rich matrix areas of the three ureilites with the most striking V‐shaped whole‐rock REE patterns (Kenna, Goalpara, and Novo Urei) were investigated using the ion imaging capability of the ion microprobe. All olivines and clinopyroxenes measured have LREE‐depleted patterns with little variation in REE abundances, despite large differences in their major element compositions from ureilite to ureilite. Furthermore, we searched for but did not find any minor mineral phases that carry LREEs. The only exception is one Ti‐rich area (～20μm) in Lewis Cliff (LEW) 85400 with a major element composition similar to that of titanite; REE abundances in this area are high, ranging from La ? 400 × CI to Lu ? 40 × CI. In contrast, all ion microprobe analyses of C‐rich matrix in Kenna, Goalpara, and Novo Urei revealed large LREE enrichments. In addition, C‐rich matrix areas in the three polymict ureilites, Elephant Moraine (EET) 83309, EET 87720, and North Haig, which have less pronounced V‐shaped whole‐rock REE patterns, show smaller but distinct LREE‐enrichments. The C‐rich matrix in Antarctic ureilites tends to have much lower LREE concentrations than the matrix in non‐Antarctic ureilites. There is no obvious association of the LREEs with other major or minor elements in the C‐rich areas. Ion images further show that the LREE enrichments are homogeneously distributed on a microscale in most C‐rich matrix areas of Kenna, Goalpara, and Novo Urei. These observations suggest that the LREEs in ureilites most probably are absorbed on the surface of fine‐grained amorphous graphite in the C‐rich matrix. It is unlikely that the LREE enrichments are due to shock melts or are the products of metasomatism on the ureilite parent body. We favor LREE introduction by terrestrial contamination.     

Presolar grains in the CM2 chondrite Sutter's Mill

The Sutter's Mill (SM) carbonaceous chondrite is a regolith breccia, composed predominantly of CM2 clasts with varying degrees of aqueous alteration and thermal metamorphism. An investigation of presolar grains in four Sutter's Mill sections, SM43, SM51, SM2‐4, and SM18, was carried out using NanoSIMS ion mapping technique. A total of 37 C‐anomalous grains and one O‐anomalous grain have been identified, indicating an abundance of 63 ppm for presolar C‐anomalous grains and 2 ppm for presolar oxides. Thirty‐one silicon carbide (SiC), five carbonaceous grains, and one Al‐oxide (Al₂O₃) were confirmed based on their elemental compositions determined by C‐N‐Si and O‐Si‐Mg‐Al isotopic measurements. The overall abundance of SiC grains in Sutter's Mill (55 ppm) is consistent with those in other CM chondrites. The absence of presolar silicates in Sutter's Mill suggests that they were destroyed by aqueous alteration on the parent asteroid. Furthermore, SM2‐4 shows heterogeneous distributions of presolar SiC grains (12–54 ppm) in different matrix areas, indicating that the fine‐grained matrix clasts come from different sources, with various thermal histories, in the solar nebula.     

Origin of the metamorphosed clasts in the CV3 carbonaceous chondrite breccias of Graves Nunataks 06101, Vigarano,Roberts Massif 04143, and Yamato‐86009

We observed metamorphosed clasts in the CV3 chondrite breccias Graves Nunataks 06101, Vigarano, Roberts Massif 04143, and Yamato‐86009. These clasts are coarse‐grained polymineralic rocks composed of Ca‐bearing ferroan olivine (Fa_24–40, up to 0.6 wt% CaO), diopside (Fs_7–12Wo_44–50), plagioclase (An_52–75), Cr‐spinel (Cr/[Cr + Al] = 0.4, Fe/[Fe + Mg] = 0.7), sulfide and rare grains of Fe‐Ni metal, phosphate, and Ca‐poor pyroxene (Fs₂₄Wo₄). Most clasts have triple junctions between silicate grains. The rare earth element (REE) abundances are high in diopside (REE ~3.80–13.83 × CI) and plagioclase (Eu ~12.31–14.67 × CI) but are low in olivine (REE ~0.01–1.44 × CI) and spinel (REE ~0.25–0.49 × CI). These REE abundances are different from those of metamorphosed chondrites, primitive achondrites, and achondrites, suggesting that the clasts are not fragments of these meteorites. Similar mineralogical characteristics of the clasts with those in the Mokoia and Yamato‐86009 breccias (Jogo et al. 2012 ) suggest that the clasts observed in this study would also form inside the CV3 chondrite parent body. Thermal modeling suggests that in order to reach the metamorphosed temperatures of the clasts of >800 °C, the clast parent body should have accreted by ~2.5–2.6 Ma after CAIs formation. The consistency of the accretion age of the clast parent body and the CV3 chondrule formation age suggests that the clasts and CV3 chondrites could be originated from the same parent body with a peak temperature of 800–1100 °C. If the body has a peak temperature of >1100 °C, the accretion age of the body becomes older than the CV3 chondrule formation age and multiple CV3 parent bodies are likely.     

Thermal metamorphic history of a Ca,Al‐rich inclusion constrained by high spatial resolution Mg isotopic measurements with NanoSIMS 50L

Abstract– Mg isotope data were collected by NanoSIMS with high‐precision and high‐spatial resolution from a coarse‐grained type B Ca‐, Al‐rich inclusion (CAI), EK1‐6‐3, in the Allende CV3 chondrite to evaluate the time scale of parent body thermal metamorphism. The CAI melilite and fassaite contain excesses of ²⁶Mg (²⁶Mg*) from the in‐situ decay of ²⁶Al; the inferred initial ratio, (²⁶Al/²⁷Al)₀ = (5.8 ± 2.4) × 10^?5, is consistent with many previously reported coarse‐grained CAIs from CV chondrites (e.g., MacPherson et al. 1995 ). However, the anorthite has heterogeneous (²⁶Al/²⁷Al)₀, ranging from 1.8 × 10^?5 to 3.3 × 10^?6. The ²⁶Al‐²⁶Mg systematics within the anorthite is consistent with thermal diffusion of Mg isotopes during metamorphism. We also show that the heterogeneous distribution of ²⁶Mg* in anorthite could have resulted from thermal diffusion of ²⁶Mg* over a 0.6–0.8 Ma time span. Mg diffusion thus may be responsible for the (²⁶Al/²⁷Al)₀ heterogeneity within anorthite in CAIs.     

Atom‐probe tomography and transmission electron microscopy of the kamacite–taenite interface in the fast‐cooled Bristol IVA iron meteorite

We report the first combined atom‐probe tomography (APT) and transmission electron microscopy (TEM) study of a kamacite–tetrataenite (K–T) interface region within an iron meteorite, Bristol (IVA). Ten APT nanotips were prepared from the K–T interface with focused ion beam scanning electron microscopy (FIB‐SEM) and then studied using TEM followed by APT. Near the K‐T interface, we found 3.8 ± 0.5 wt% Ni in kamacite and 53.4 ± 0.5 wt% Ni in tetrataenite. High‐Ni precipitate regions of the cloudy zone (CZ) have 50.4 ± 0.8 wt% Ni. A region near the CZ and martensite interface has <10 nm sized Ni‐rich precipitates with 38.4 ± 0.7 wt% Ni present within a low‐Ni matrix having 25.5 ± 0.6 wt% Ni. We found that Cu is predominantly concentrated in tetrataenite, whereas Co, P, and Cr are concentrated in kamacite. Phosphorus is preferentially concentrated along the K‐T interface. This study is the first precise measurement of the phase composition at high spatial resolution and in 3‐D of the K‐T interface region in a IVA iron meteorite and furthers our knowledge of the phase composition changes in a fast‐cooled iron meteorite below 400 °C. We demonstrate that APT in conjunction with TEM is a useful approach to study the major, minor, and trace elemental composition of nanoscale features within fast‐cooled iron meteorites.     

Determination of volatile concentrations in fluorapatite of Martian shergottite NWA 2975 by combining synchrotron FTIR,Raman spectroscopy,EMPA, and TEM,and inferences on the volatile budget of the apatite host‐magma

We combined the focused ion beam sample preparation technique with polarized synchrotron‐based FTIR (Fourier transform infrared) spectroscopy, laser‐Raman spectroscopy, electron microprobe analysis (EMPA), and transmission electron microscope (TEM) analysis to identify and quantify structurally bound OH, F, Cl, and CO₃ groups in fluorapatite from the Northwest Africa 2975 (NWA 2975) shergottite. In this study, the first FTIR spectra of the OH‐stretching region from a Martian apatite are presented that show characteristic OH‐bands of a F‐rich, hydroxyl‐bearing apatite. Depending on the method of apatite‐formula calculation and whether charge balance is assumed or not, the FTIR‐based quantification of the incorporated OH, expressed as wt% H₂O, is in variably good agreement with the H₂O concentration calculated from electron microprobe data. EMP analyses yielded between 0.35 and 0.54 wt% H₂O, and IR data yielded an average H₂O content of 0.31 ± 0.03 wt%, consistent with the lower range determined from EMP analyses. The TEM observations implied that the volatiles budget of fluorapatite is magmatic. The water content and the relative volatile ratios calculated for the NWA 2975 magma are similar to those established for other enriched or intermediate shergottites. It is difficult to define the source of enrichment: either Martian wet mantle or crustal assimilation. Comparing the environment of parental magma generation for NWA 2975 with the terrestrial mantle in terms of water content, it displays a composition intermediate between enriched and depleted MORB.     

Metamorphosed calcium‐aluminum‐rich inclusions in CK carbonaceous chondrites

CK chondrites are the only group of carbonaceous chondrites with petrologic types ranging from 3 to 6. Although CKs are described as calcium‐aluminum‐rich inclusion (CAI)‐poor objects, the abundance of CAIs in the 18 CK3–6 we analyzed ranges from zero to approximately 16.4%. During thermal metamorphism, some of the fine‐grained CAIs recrystallized as irregular assemblages of plagioclase + Ca‐rich pyroxene ± olivine ± Ca‐poor pyroxene ± magnetite. Coarse‐grained CAIs display zoned spinel, fassaite destabilization, and secondary grossular and spinel. Secondary anorthite, grossular, Ca‐rich pyroxene, and spinel derive from the destabilization of melilite, which is lacking in all CAIs investigated. The Al‐Mg isotopic systematics measured in fine‐ and coarse‐grained CAIs from Tanezrouft (Tnz) 057 was affected by Mg redistribution. The partial equilibration of Al‐Mg isotopic signatures obtained in the core of a coarse‐grained CAI (CG1‐CAI) in Tnz 057 may indicate a lower peak temperature for Mg diffusion of approximately 540–580 °C, while grossular present in the core of this CAI indicates a higher temperature of around 800 °C for the metamorphic event on the parent body of Tnz 057. Excluding metamorphic features, the similarity in nature and abundance of CAIs in CK and CV chondrites confirms that CVs and CKs form a continuous metamorphic series from type 3 to 6.     

Isotopic compositions,nitrogen functional chemistry,and low‐loss electron spectroscopy of complex organic aggregates at the nanometer scale in the carbonaceous chondrite Renazzo

Organic matter (OM) was widespread in the early solar nebula and might have played an important role for the delivery of prebiotic molecules to the early Earth. We investigated the textures, isotopic compositions, and functional chemistries of organic grains in the Renazzo carbonaceous chondrite by combined high spatial resolution techniques (electron microscopy–secondary ion mass spectrometry). Morphologies are complex on a submicrometer scale, and some organics exhibit a distinct texture with alternating layers of OM and minerals. These layered organics are also characterized by heterogeneous ¹⁵N isotopic abundances. Functional chemistry investigations of five focused ion beam‐extracted lamellae by electron energy loss spectroscopy reveal a chemical complexity on a nanometer scale. Grains show absorption at the C‐K edge at 285, 286.6, 287, and 288.6 eV due to polyaromatic hydrocarbons, different carbon‐oxygen, and aliphatic bonding environments with varying intensity. The nitrogen K‐edge functional chemistry of three grains is shown to be highly complex, and we see indications of amine (C‐NH_x) or amide (CO‐NR₂) chemistry as well as possible N‐heterocycles and nitro groups. We also performed low‐loss vibrational spectroscopy with high energy resolution and identified possible D‐ and G‐bands known from Raman spectroscopy and/or absorption from C=C and C‐O stretch modes known from infrared spectroscopy at around 0.17 and 0.2 eV energy loss. The observation of multiglobular layered organic aggregates, heterogeneous ¹⁵N‐anomalous compositions, and indication of NH_x‐(amine) functional chemistry lends support to recent ideas that ¹⁵N‐enriched ammonia (NH₃) was a powerful agent to synthesize more complex organics in aqueous asteroidal environments.     

Siderophile and chalcophile element abundances in shergottites: Implications for Martian core formation

Elemental abundances for volatile siderophile and chalcophile elements for Mars inform us about processes of accretion and core formation. Such data are few for Martian meteorites, and are often lacking in the growing number of desert finds. In this study, we employed laser ablation inductively coupled plasma–mass spectrometry (LA‐ICP‐MS) to analyze polished slabs of 15 Martian meteorites for the abundances of about 70 elements. This technique has high sensitivity, excellent precision, and is generally accurate as determined by comparisons of elements for which literature abundances are known. However, in some meteorites, the analyzed surface is not representative of the bulk composition due to the over‐ or underrepresentation of a key host mineral, e.g., phosphate for rare earth elements (REE). For other meteorites, the range of variation in bulk rastered analyses of REE is within the range of variation reported among bulk REE analyses in the literature. An unexpected benefit has been the determination of the abundances of Ir and Os with a precision and accuracy comparable to the isotope dilution technique. Overall, the speed and small sample consumption afforded by this technique makes it an important tool widely applicable to small or rare meteorites for which a polished sample was prepared. The new volatile siderophile and chalcophile element abundances have been employed to determine Ge and Sb abundances, and revise Zn, As, and Bi abundances for the Martian mantle. The new estimates of Martian mantle composition support core formation at intermediate pressures (14 ± 3 GPa) in a magma ocean on Mars.     

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.     

SIMS U-Pb dating of micro-zircons in the lunar meteorites Dhofar 1528 and Dhofar 1627

About half of the lunar meteorites in our collections are feldspathic breccias. Acquiring geochronologic information from these breccias is challenging due to their low radioactive-element contents and their often polymict nature. We used high-spatial-resolution (5 μm) NanoSIMS (nanoscale secondary ion mass spectrometry) U-Pb dating technique to date micro-zircons in the lunar feldspathic meteorites Dhofar 1528 and Dhofar 1627. Three NanoSIMS dating spots of two zircon grains from Dhofar 1528 show a discordia with an upper intercept at 4354 ± 76 Ma and a lower intercept at 332 ± 1407 Ma (2σ, MSWD = 0.01, p = 0.91). Three spots of two zircon grains in Dhofar 1627 define a discordia with an upper intercept at 3948 ± 30 Ma and a lower intercept at 691 ± 831 Ma (2σ, MSWD = 0.40, p = 0.53). Both samples likely experienced shock metamorphism caused by impacts. Based on the clastic nature, lack of recrystallization and the consistent U-Pb and Pb-Pb dates of the zircons in Dhofar 1528, the U-Pb date of 4354 Ma is interpreted as the crystallization age of its Mg-suite igneous precursor. Some of the Dhofar 1627 zircons show poikilitic texture, a crystallization from the matrix impact melt, so the U-Pb date of 3948 Ma corresponds to an impact event, likely the Imbrium basin-forming event. These data are the first radiometric ages for these two meteorites and demonstrate that in situ (high spatial resolution) U-Pb dating has potential for extracting geochronological information about igneous activities and impact events from lunar feldspathic and polymict breccias.     

Characterization of weathering and heterogeneous mineral phase distribution in brachinite Northwest Africa 4872

Terrestrial weathering of hot desert achondrite meteorite finds and heterogeneous phase distributions in meteorites can complicate interpretation of petrological and geochemical information regarding parent‐body processes. For example, understanding the effects of weathering is important for establishing chalcophile and siderophile element distributions within sulfide and metal phases in meteorites. Heterogeneous mineral phase distribution in relatively coarsely grained meteorites can also lead to uncertainties relating to compositional representativeness. Here, we investigate the weathering and high‐density (e.g., sulfide, spinel, Fe‐oxide) phase distribution in sections of ultramafic achondrite meteorite Northwest Africa (NWA) 4872. NWA 4872 is an olivine‐rich brachinite (Fo_{63.6 ± 0.5}) with subsidiary pyroxene (Fs_9.7 ± 0.1Wo_{46.3 ± 0.2}), Cr‐spinel (Cr# = 70.3 ± 1.1), and weathered sulfide and metal. Raman mapping confirms that weathering has redistributed sulfur from primary troilite, resulting in the formation of Fe‐oxide (‐hydroxide) and marcasite (FeS₂). From Raman mapping, NWA 4872 is composed of olivine (89%), Ca‐rich pyroxene (0.4%), and Cr‐spinel (1.1%), with approximately 7% oxidized metal and sulfide and 2.3% marcasite‐dominated sulfide. Microcomputed tomography (micro‐CT) observations reveal high‐density regions, demonstrating heterogeneities in mineral distribution. Precision cutting of the largest high‐density region revealed a single 2 mm Cr‐spinel grain. Despite the weathering in NWA 4872, rare earth element (REE) abundances of pyroxene determined by laser‐ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) indicate negligible modification of these elements in this mineral phase. The REE abundances of mineral grains in NWA 4872 are consistent with formation of the meteorite as the residuum of the partial melting process that occurred on its parent body. LA‐ICP‐MS analyses of sulfide and alteration products demonstrate the mobility of Re and/or Os; however, highly siderophile element (HSE) abundance patterns remain faithful recorders of processes acting on the brachinite parent body(ies). Detailed study of weathering and phase distribution offers a powerful tool for assessing the effects of low‐temperature alteration and for identifying robust evidence for parent‐body processes.     

Presolar grains in primitive ungrouped carbonaceous chondrite Northwest Africa 5958

We report a correlated NanoSIMS‐transmission electron microscopy study of the ungrouped carbonaceous chondrite Northwest Africa (NWA) 5958. We identified 10 presolar SiC grains, 2 likely presolar graphite grains, and 20 presolar silicate and/or oxide grains in NWA 5958. We suggest a slight modification of the commonly used classification system for presolar oxides and silicates that better reflects the grains’ likely stellar origins. The matrix‐normalized presolar SiC abundance in NWA 5958 is ppm (2σ) similar to that seen in many classes of unmetamorphosed chondrites. In contrast, the matrix‐normalized abundance of presolar O‐rich phases (silicates and oxides) is ppm (2σ), much lower than seen in interplanetary dust particles and the least‐altered CR, CO, and ungrouped C chondrites, but close to that reported for CM chondrites. NanoSIMS mapping also revealed an unusual ¹³C‐enriched (δ¹³C≈100–200‰) carbonaceous rim surrounding a 1.4 μm diameter phyllosilicate grain. Transmission electron microscopy (TEM) analysis of two presolar grains with a likely origin in asymptotic giant branch stars identified one as enstatite and one as Al‐Mg spinel with minor Cr. The enstatite grain amorphized rapidly under the electron beam, suggesting partial hydration. TEM data of NWA 5958 matrix confirm that it has experienced aqueous alteration and support the suggestion of Jacquet et al. (34) that this meteorite has affinities to CM2 chondrites.     

Hyperspectral mapping of alteration assemblages within a hydrothermal vug at the Haughton impact structure,Canada

Meteorite impacts on Earth and Mars can generate hydrothermal systems that alter the primary mineralogies of rocks and provide suitable environments for microbial colonization. We investigate a calcite–marcasite‐bearing vug at the ~23 km diameter Haughton impact structure, Devon Island, Nunavut, Canada, using imaging spectroscopy of the outcrop in the field (0.65–1.1 μm) and samples in the laboratory (0.4–2.5 μm), point spectroscopy (0.35–2.5 μm), major element chemistry, and X‐ray diffraction analyses. The mineral assemblages mapped at the outcrop include marcasite; marcasite with minor gypsum and jarosite; fibroferrite and copiapite with minor gypsum and melanterite; gypsum, Fe³⁺ oxides, and jarosite; and calcite, gypsum, clay, microcline, and quartz. Hyperspectral mapping of alteration phases shows spatial patterns that illuminate changes in alteration conditions and formation of specific mineral phases. Marcasite formed from the postimpact hydrothermal system under reducing conditions, while subsequent weathering oxidized the marcasite at low temperatures and water/rock ratios. The acidic fluids resulting from the oxidation collected on flat‐lying portions of the outcrop, precipitating fibroferrite + copiapite. That assemblage then likely dissolved, and the changing chemistry and pH resulting from interaction with the calcite‐rich host rock formed gypsum‐bearing red coatings. These results have implications for understanding water–rock interactions and habitabilities at this site and on Mars.     

A cornucopia of presolar and early solar system materials at the micrometer size range in primitive chondrite matrix

Abstract— We have used a variety of complementary microanalytical techniques to constrain the mineralogy, trace‐element distributions, and oxygen‐isotopic compositions in a 50 × 50 μm area of Acfer 094 matrix. The results reveal the exceptional mineralogical and compositional heterogeneity of this material at the sub‐μm level. We observe μm‐scale and sub‐μm grains with elemental associations suggesting feldspar, metal with widely varying Ni contents, and a Cr‐Fe alloy (in addition to forsterite, pyroxene, sulfide, ferrihydrite, and amorphous groundmass previously described). A new class of μm‐scale CAI (μCAI) is also observed, which show sub‐μm compositional zoning, and a range of oxygen isotopic compositions. Unlike the larger CAIs in Acfer 094, which are uniformly ¹⁶O‐enriched, two of the three μCAIs we analyzed are isotopically normal. We also observed a Li‐rich hotspot that detailed analysis by ToF‐SIMS suggests may be a LiCr‐oxide grain. Within the resolution of the NanoSIMS, this grain has isotopically normal Li. Finally, in our 50 × 50 μm area, we positively identified a presolar grain that is the most ¹⁸O‐rich silicate found so far in meteorites. The grain may originate from an asymptotic giant branch (AGB) star, or more likely, a supernova. In line with previous TEM studies (Greshake 1997), we find no evidence for clastic material (e.g., fragmental chondrules) in the matrix of Acfer 094: although the matrix is volatile‐depleted, this depletion does not appear to result from dilution of a primordial starting material with (depleted) chondrule fragments. Assuming that matrix experienced the depletion event, our data on the detailed mineralogy of Acfer 094 are currently equivocal in constraining the nature of that event. We observe carrier phases for several elements consistent with conditions approaching equilibrium condensation; however, the presence of an amorphous groundmass is suggestive of more rapid cooling.     

In situ determination of iodine content and iodine-xenon systematics in silicates and troilite phases in chondrules from the LL3 chondrite Semarkona

Abstract— Iodine concentrations in small domains (～10 μm) of silicates and troilite (FeS) phases in three chondrules from the Semarkona (LL3) meteorite were determined by an ion microprobe. Independent determination of I content in some of these phases was accomplished by in situ laser probe mass spectrometric analysis of I-derived ¹²⁸Xe in one of these neutron-irradiated chondrules. The ion microprobe data suggest low I content for olivines (20–45 ppb) and relatively higher values for pyroxene and glass (mesostasis) (40–160 ppb). The broad similarity in the measured I contents in pyroxenes in a porphyritic pyroxene chondrule by ion microprobe (42–138 ppb) and by laser probe (37–76 ppb) demonstrate the feasibility of in situ determination of I content in silicate phases via ion microprobe. The I contents in troilite measured by ion microprobe, however, are prone to uncertainty because of the lack of a sulfide standard. The ion microprobe data suggest I content of > 1 ppm in troilite, if the calibration from our silicate standard is used. However, the noble gas data suggest that the I content in troilite is comparable to that in silicates. We attribute this apparent discrepancy to an enhanced sputter ion yield of I from sulfides. Iodine-derived ¹²⁹Xe excesses were observed in both pyroxene and troilite within this chondrule. The I-Xe model ages of these selected phases are consistent with the I-Xe studies of the bulk chondrule. The individual data points fall on or near the isochron obtained from the bulk chondrule, although all except the most radiogenic data point contain evidence of low-temperature uncorrelated iodine.