Chromium isotopic systematics of the Sutter's Mill carbonaceous chondrite: Implications for isotopic heterogeneities of the early solar system

Recent studies have shown that major meteorite groups possess their own characteristic ⁵⁴Cr values, demonstrating the utility of Cr isotopes for identifying genetic relationships between the planetary materials in conjunction with other classical tools, such as oxygen isotopes. In this study, we performed Cr isotope analyses for whole rocks and chemically separated phases of the new CM2 chondrite, Sutter's Mill (SM 43 and 51). The two whole rocks of Sutter's Mill show essentially identical ε⁵⁴Cr excesses (SM 43 = +0.95 ± 0.09ε, SM 51 = +0.88 ± 0.07ε), relative to the Earth. These values are the same within error with that of the CM2‐type Murchison (+0.89 ± 0.08ε), suggesting that parent bodies of Sutter's Mill and Murchison were formed from the same precursor materials in the solar nebula. Large ε⁵⁴Cr excess of up to 29.40ε is observed in the silicate phase of Sutter's Mill, while that of Murchison shows 15.74ε. Importantly, the leachate fractions of both Sutter's Mill and Murchison form a steep linear anticorrelation between ε⁵⁴Cr and ε⁵³Cr, cross‐cutting the positive correlation previously observed in carbonaceous chondrites. The fact that L4 acid leachate fraction contains higher ⁵⁴Cr excesses than that of L5 step designed to dissolve refractory minerals suggests that spinel is not a major ⁵⁴Cr carrier. We also note that L5 contains ⁵³Cr anomalies lower than the solar initial value, suggesting it carries a component of nucleosynthetic anomaly unrelated to the ⁵³Mn decay. We have identified five endmember components of nucleosynthetic origin among the early solar system materials.     

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.     

Infrared imaging spectroscopy with micron resolution of Sutter's Mill meteorite grains

Synchrotron‐based Fourier transform infrared spectroscopy and Raman spectroscopy are applied with submicrometer spatial resolution to multiple grains of Sutter's Mill meteorite, a regolith breccia with CM1 and CM2 lithologies. The Raman and infrared active functional groups reveal the nature and distribution of organic and mineral components and confirm that SM12 reached higher metamorphism temperatures than SM2. The spatial distributions of carbonates and organic matter are negatively correlated. The spatial distributions of aliphatic organic matter and OH relative to the distributions of silicates in SM2 differ from those in SM12, supporting a hypothesis that the parent body of Sutter's Mill is a combination of multiple bodies with different origins. The high aliphatic CH₂/CH₃ ratios determined from band intensities for SM2 and SM12 grains are similar to those of IDPs and less altered carbonaceous chondrites, and they are significantly higher than those in other CM chondrites and diffuse ISM objects.     

Mn‐Cr isotope systematics of the D'Orbigny angrite

Abstract— We have conducted a detailed study of the Mn‐Cr systematics of the angrite D'Orbigny. Here, we report Cr isotopic abundances and Mn/Cr ratios in olivine, pyroxene, glass, chromite, and bulk rock samples from D'Orbigny. ⁵³Cr excesses in these samples correlate well with their respective Mn/Cr ratios and define an isochron with a slope that corresponds to an initial ⁵³Mn/⁵⁵Mn ratio = (3.24 ± 0.04) × 10^?6 and initial ⁵³Cr/⁵²Cr ratio of ?(53) = 0.30 ± 0.03 at the time of isotopic closure. The ⁵³Mn/⁵⁵Mn ratio of the D'Orbigny bulk rock is more than two‐fold the ⁵³Mn/⁵⁵Mn ratio of the angrites Lewis Cliff 86010 (LEW) and Angra dos Reis (ADOR) and implies an older Mn‐Cr age of 4562.9 ± 0.6 Ma for D'Orbigny relative to a Pb‐Pb age of 4557.8 ± 0.5 Ma for LEW and ADOR. One of the most unusual aspects of D'Orbigny is the presence of glass, a phase that has not been identified in any of the other angrites. The Mn‐Cr data for glass and a pyroxene fraction found in druses indicate that they formed contemporaneously with the main phases of the meteorite. Since the Mn‐Cr age of D'Orbigny is ?5 Ma years older than the angrites LEW and ADOR, D'Orbigny likely represents an earlier stage in the evolution of the angrite parent body.     

The secondary history of Sutter's Mill CM carbonaceous chondrite based on water abundance and the structure of its organic matter from two clasts

Sutter's Mill is a regolith breccia composed of both heavily altered clasts and more reduced xenoliths. Here, we present a detailed investigation of fragments of SM18 and SM51. We have characterized the water content and the mineralogy by infrared (IR) and thermogravimetric analysis (TGA) and the structure of the organic compounds by Raman spectroscopy, to characterize the secondary history of the clasts, including aqueous alteration and thermal metamorphism. The three methods used in this study suggest that SM18 was significantly heated. The amount of water contained in phyllosilicates derived by TGA is estimated to be approximately 3.2 wt%. This value is quite low compared with other CM chondrites that typically range from 6 to 12 wt%. The infrared transmission spectra of SM18 show that the mineralogy of the sample is dominated by a mixture of phyllosilicate and olivine. SM18 shows an intense peak at 11.2 μm indicative of olivine (Fig. 1). If we compare SM18 with other CM and metamorphosed CM chondrites, it shows one of the most intense olivine signatures, and therefore a lower proportion of phyllosilicate minerals. The Raman results tend to support a short‐duration heating hypothesis. In the I_D/I_G versus FWHM‐D diagram, SM18 appears to be unusual compared to most CM samples, and close to the metamorphosed CM chondrites Pecora Escarpment (PCA) 91008 and PCA 02012. In the case of SM51, infrared spectroscopy reveals that olivine is less abundant than in SM18 and the 10 μm silicate feature is more similar to that of moderately altered CM chondrites (like Murchison or Queen Alexandra Range [QUE] 97990). Raman spectroscopy does not clearly point to a heating event for SM51 in the I_D/I_G versus FWHM‐D diagram. However, TGA analysis suggests that SM51 was slightly dehydrated as the amount of water contained in phyllosilicates is approximately 3.7 wt%, which is higher than SM18, but still lower than phyllosilicate water contents in weakly altered CM chondrites. Altogether, these results confirm that fragments with different secondary histories are present within the Sutter's Mill fall. The dehydration that is clearly observed for SM18 is attributed to a short‐duration heating based on the similarity of its Raman spectra to that of PCA 91008. Because of the brecciated nature of Sutter's Mill and the presence of adjacent clasts with different thermal histories, impacts that can efficiently fragment and heat porous materials are the preferred heat source.     

53Mn‐53Cr ages of Kaidun carbonates

Abstract– We report the ⁵³Mn‐⁵³Cr systematics of three dolomite grains from two different CI1 clasts contained within the Kaidun meteorite breccia. Three internal isochrones result in initial ⁵³Mn/⁵⁵Mn ratios of (4.2 ± 0.4) × 10^?6, (4.6 ± 1.3) × 10^?6, and (5.2 ± 1.1) × 10^?6. These initial values are consistent with those measured for dolomite in the Orgueil CI1 chondrite ( Hoppe et al. 2007 ; Petitat et al. 2009 ) but significantly lower than the initial ratio determined by Hutcheon et al. (1999) from a combination of different carbonate types within various lithologies of the Kaidun meteorite. We construct an accretion scenario for the Kaidun breccia by comparing the mineralogy and formation time scales of carbonates in the Kaidun CI1 lithologies to the analogous ones of the CI1 chondrite Orgueil. In Orgueil, dolomite precipitation precedes the formation of the first bruennerite grains by a few million years ( Hoppe et al. 2007 ; Petitat et al. 2009 ). As the CI1 clasts in Kaidun lack breunnerite grains, and considering that aqueous alteration occurred prior to reaccretion of the various clasts onto the Kaidun parent body (e.g., MacPherson et al. 2009 ), we hypothesize that after rapid accretion and early aqueous alteration occurring within the first approximately 4 Myr after solar system formation, impact disruption of several asteroids and their reassembly into the Kaidun parent asteroid was complete within an additional approximately 2 Myr. This confirms that aqueous alteration, impact, and reaccretion of material in the asteroid belt were early processes that began contemporaneously with chondrule formation.     

Magnesium isotopic fractionation in chondrules from the Murchison and Murray CM2 carbonaceous chondrites

We present high‐precision measurements of the Mg isotopic compositions of a suite of types I and II chondrules separated from the Murchison and Murray CM2 carbonaceous chondrites. These chondrules are olivine‐ and pyroxene‐rich and have low ²⁷Al/²⁴Mg ratios (0.012–0.316). The Mg isotopic compositions of Murray chondrules are on average lighter (δ²⁶Mg ranging from ?0.95‰ to ?0.15‰ relative to the DSM‐3 standard) than those of Murchison (δ²⁶Mg ranging from ?1.27‰ to +0.77‰). Taken together, the CM2 chondrules exhibit a narrower range of Mg isotopic compositions than those from CV and CB chondrites studied previously. The least‐altered CM2 chondrules are on average lighter (average δ²⁶Mg = ?0.39 ± 0.30‰, 2SE) than the moderately to heavily altered CM2 chondrules (average δ²⁶Mg = ?0.11 ± 0.21‰, 2SE). The compositions of CM2 chondrules are consistent with isotopic fractionation toward heavy Mg being associated with the formation of secondary silicate phases on the CM2 parent body, but were also probably affected by volatilization and recondensation processes involved in their original formation. The low‐Al CM2 chondrules analyzed here do not exhibit any mass‐independent variations in ²⁶Mg from the decay of ²⁶Al, with the exception of two chondrules that show only small variations just outside of the analytical error. In the case of the chondrule with the highest Al/Mg ratio (a type IAB chondrule from Murchison), the lack of resolvable ²⁶Mg excess suggests that it either formed >1 Ma after calcium‐aluminum‐rich inclusions, or that its Al‐Mg isotope systematics were reset by secondary alteration processes on the CM2 chondrite parent body after the decay of ²⁶Al.     

Rapid effects of terrestrial alteration on highly siderophile elements in the Sutter's Mill meteorite

The ¹⁸⁷Re-¹⁸⁷Os isotopic systematics of many bulk chondrites plot well beyond analytical uncertainties of a primordial isochron. Limited variations in ¹⁸⁷Os/¹⁸⁸Os, coupled with large variations in Re/Os ratios among chondrites, suggest that this apparently open-system behavior is a result of the comparatively recent gain or loss of Re and/or Os. In order to assess whether or not rapid alteration in the terrestrial environment could be responsible for open-system behavior in chondrites, four pieces of the Sutter's Mill meteorite were examined for Os isotopic systematics and abundances of highly siderophile elements. Pieces SM1 and SM2 were collected prior to a rain event, within 2 days of the fall. Pieces SM51 and SM53 were collected after a rain event. There are significant but minor relative and absolute variations in the abundances of the highly siderophile elements, as well as ¹⁸⁷Os/¹⁸⁸Os among the four pieces. Rhenium-Os isotopic data for SM1 and SM2 plot within analytical uncertainties of a primordial isochron, while powders made from SM51 and SM53 do not. These results suggest that interactions with rain caused some redistribution of Re, and to a lesser extent Os, within small pieces of the meteorite. Thus, Re-Os isotopic systematics of <dm-size pieces of chondrites must be considered susceptible to modification after only a short time on the surface, where exposed to rain.     

Mineralogy and petrography of C asteroid regolith: The Sutter's Mill CM meteorite

Based upon our characterization of three separate stones by electron and X‐ray beam analyses, computed X‐ray microtomography, Raman microspectrometry, and visible‐IR spectrometry, Sutter's Mill is a unique regolith breccia consisting mainly of various CM lithologies. Most samples resemble existing available CM2 chondrites, consisting of chondrules and calcium‐aluminum‐rich inclusion (CAI) set within phyllosilicate‐dominated matrix (mainly serpentine), pyrrhotite, pentlandite, tochilinite, and variable amounts of Ca‐Mg‐Fe carbonates. Some lithologies have witnessed sufficient thermal metamorphism to transform phyllosilicates into fine‐grained olivine, tochilinite into troilite, and destroy carbonates. One finely comminuted lithology contains xenolithic materials (enstatite, Fe‐Cr phosphides) suggesting impact of a reduced asteroid (E or M class) onto the main Sutter's Mill parent asteroid, which was probably a C class asteroid. One can use Sutter's Mill to help predict what will be found on the surfaces of C class asteroids such as Ceres and the target asteroids of the OSIRIS‐REx and Hayabusa 2 sample return missions (which will visit predominantly primitive asteroids). C class asteroid regolith may well contain a mixture of hydrated and thermally dehydrated indigenous materials as well as a significant admixture of exogenous material would be essential to the successful interpretation of mineralogical and bulk compositional data.     

The Sutter's Mill meteorite: Thermoluminescence data on thermal and metamorphic history

A piece of the Sutter's Mill meteorite, fragment SM2‐1d, has been examined using thermoluminescence techniques to better understand its thermal and metamorphic history. The sample had very weak but easily measureable natural and induced thermoluminescence (TL) signals; the signal‐to‐noise ratio was better than 10. The natural TL was restricted to the high‐temperature regions of the glow curve suggesting that the meteorite had been heated to approximately 300 °C within the time it takes for the TL signal to recover from a heating event, probably within the last 10⁵ years. It is possible that this reflects heating during release from the parent body, close passage by the Sun, or heating during atmospheric passage. Of these three options, the least likely is the first, but the other possibilities are equally likely. It seems that temperatures of approximately 300 °C reached 5 or 6 mm into the meteorite, so that all but one of the small Sutter's Mill stones have been heated. The Dhajala normalized induced TL signal for SM2‐1d is comparable to that of type 3.0 chondrites and is unlike normal CM chondrites, the class it most closely resembles, which do not have detectable TL sensitivity. The shape of the induced TL curve is comparable to other low‐type ordinary, CV, and CO chondrites, in that it has a broad hummocky structure, but does not resemble any of them in detail. This suggests that Sutter's Mill is a unique, low‐petrographic–type (3.0) chondrite.     

Carbonates in CM chondrites: Complex formational histories and comparison to carbonates in CI chondrites

Abstract– CM chondrites are primitive solar‐system materials that have undergone high degrees of aqueous alteration, resulting in the formation of secondary minerals including carbonates. Two different carbonate minerals (calcite/aragonite and dolomite) together constitute 1.4–2.8 vol% of CM chondrites. In contrast, CI chondrites contain four different carbonate minerals: calcite/aragonite, dolomite, breunnerite, and siderite. CI chondrites have abundant dolomite, a mineral that seems to be absent in the most aqueously altered CM chondrites. In this study, carbonates in seven CM chondrites (Y‐791198, LaPaz Icefield 04796, Cold Bokkeveld, Nogoya, Queen Alexandra Range 93005, Allan Hills 83100, and Meteorite Hills 01070) were studied petrographically and by electron microprobe. The results indicate that carbonate formation in CM chondrites differs from that in CI chondrites and is more complex than previously recognized. Our studies of CM chondrites indicate that (1) carbonates formed on the parent asteroid in an aqueous environment that gradually changed in composition, (2) at some stage, Ca and Mg activities in the environment were high enough to form metastable dolomite, and (3) dolomites disappeared in the most aqueously altered CM chondrites.     

The presolar grain inventory of fine‐grained chondrule rims in the Mighei‐type (CM) chondrites

We investigated the inventory of presolar silicate, oxide, and silicon carbide (SiC) grains of fine‐grained chondrule rims in six Mighei‐type (CM) carbonaceous chondrites (Banten, Jbilet Winselwan, Maribo, Murchison, Murray and Yamato 791198), and the CM‐related carbonaceous chondrite Sutter's Mill. Sixteen O‐anomalous grains (nine silicates, six oxides) were detected, corresponding to a combined matrix‐normalized abundance of ~18 ppm, together with 21 presolar SiC grains (~42 ppm). Twelve of the O‐rich grains are enriched in ¹⁷O, and could originate from low‐mass asymptotic giant branch stars. One grain is enriched in ¹⁷O and significantly depleted in ¹⁸O, indicative of additional cool bottom processing or hot bottom burning in its stellar parent, and three grains are of likely core‐collapse supernova origin showing enhanced ¹⁸O/¹⁶O ratios relative to the solar system ratio. We find a presolar silicate/oxide ratio of 1.5, significantly lower than the ratios typically observed for chondritic meteorites. This may indicate a higher degree of aqueous alteration in the studied meteorites, or hint at a heterogeneous distribution of presolar silicates and oxides in the solar nebula. Nevertheless, the low O‐anomalous grain abundance is consistent with aqueous alteration occurring in the protosolar nebula and/or on the respective parent bodies. Six O‐rich presolar grains were studied by Auger Electron Spectroscopy, revealing two Fe‐rich silicates, one forsterite‐like Mg‐rich silicate, two Al‐oxides with spinel‐like compositions, and one Fe‐(Mg‐)oxide. Scanning electron and transmission electron microscopic investigation of a relatively large silicate grain (490 nm × 735 nm) revealed that it was crystalline åkermanite (Ca₂Mg[Si₂O₇]) or a an åkermanite‐diopside (MgCaSi₂O₆) intergrowth.     

The amino acid and hydrocarbon contents of the Paris meteorite: Insights into the most primitive CM chondrite

The Paris meteorite is one of the most primitive carbonaceous chondrites. It is reported to be the least aqueously altered CM chondrite, and to have experienced only weak thermal metamorphism. We have analyzed for the first time the amino acid and hydrocarbon contents of this pristine meteorite by gas chromatography–mass spectrometry (GC–MS). When plotting the relative amino acids abundances of several CM chondrites according to the increasing hydrothermal scale (petrologic subtypes), from the CM2.7/2.8 Paris to the CM2.0 MET 01070, Paris has the lowest relative abundance of β‐alanine/glycine (0.15), which fits with the relative abundances of β‐alanine/glycine increasing with increasing aqueous alteration for CM chondrites. These results confirm the influence of aqueous alteration on the amino acid abundances and distribution. The amino acid analysis shows that the isovaline detected in this meteorite is racemic (d /l  = 0.99 ± 0.08; l ‐enantiomer excess = 0.35 ± 0.5%; corrected d /l  = 1.03; corrected l ‐enantiomer excess = ?1.4 ± 2.6%). The identified hydrocarbons show that Paris has n‐alkanes ranging from C₁₆ to C₂₅ and 3‐ to 5‐ring nonalkylated polycyclic aromatic hydrocarbons (PAHs). The lack of alkylated PAHs in Paris seems to be also related to this low degree of aqueous alteration on its parent body. The extraterrestrial hydrocarbon content, suggested by the absence of any biomarker, may well have a presolar origin. The chemistry of the Paris meteorite may thus be closely related to the early stages of the solar nebula with a contribution from interstellar (molecular cloud) precursors.     

Exposure history of the Sutter's Mill carbonaceous chondrite

The Sutter's Mill (SM) carbonaceous chondrite fell in California on April 22, 2012. The cosmogenic radionuclide data indicate that Sutter's Mill was exposed to cosmic rays for 0.082 ± 0.008 Myr, which is one of the shortest ages for C chondrites, but overlaps with a small cluster at approximately 0.1 Myr. The age is significantly longer than proposed ages that were obtained from cosmogenic noble gas concentrations, which have large uncertainties due to trapped noble gas corrections. The presence of neutron‐capture ⁶⁰Co and ³⁶Cl in SM indicates a minimum preatmospheric radius of approximately 50 cm, and is consistent with a radius of 1–2 m, as derived from the fireball observations. Although a large preatmospheric size was proposed, one fragment (SM18) contains solar cosmic ray–produced short‐lived radionuclides, such as ⁵⁶Co and ⁵¹Cr. This implies that this specimen was less than 2 cm from the preatmospheric surface of Sutter's Mill. Although this conclusion seems surprising, it is consistent with the observation that the meteoroid fragmented high in the atmosphere. The presence of SCR‐produced nuclides is consistent with the high SCR fluxes observed during the last few months before the meteorite's fall, when its orbit was less than 1 AU from the Sun.     

P‐O‐rich sulfide phase in CM chondrites: Constraints on its origin on the CM parent body

CM chondrites are a group of primitive meteorites that have recorded the alteration history of the early solar system. We report the occurrence, chemistry, and oxygen isotopic compositions of P‐O‐rich sulfide phase in two CM chondrites (Grove Mountains [GRV] 021536 and Murchison). This P‐O‐rich sulfide is a polycrystalline aggregate of nanometer‐size grains. It occurs as isolated particles or aggregates in both CM chondrites. These grains, in the matrix and in type‐I chondrules from Murchison, were partially altered into tochilinite; however, grains enclosed by Ca‐carbonate are much less altered. This P‐O‐rich sulfide in Murchison is closely associated with magnetite, FeNi phosphide, brezinaite (Cr₃S₄), and eskolaite (Cr₂O₃). In addition to sulfur as the major component, this sulfide contains ~6.3 wt% O, ~5.4 wt% P, and minor amounts of hydrogen. Analyses of oxygen isotopes by SIMS resulted in an average δ¹⁸O value of ?22.5 ‰ and an average Δ¹⁷O value of 0.2 ± 9.2 ‰ (2σ). Limited variations in both chemical compositions and electron‐diffraction patterns imply that the P‐O‐rich sulfide may be a single phase rather than a polyphase mixture. Several features indicate that this P‐O‐rich sulfide phase formed at low temperature on the parent body, most likely through the alteration of FeNi metal (a) close association with other low‐temperature alteration products, (b) the presence of hydrogen, (c) high Δ¹⁷O values and the presence in altered mesostasis of type‐I chondrules and absence in type‐II chondrules. The textural relations of the P‐O‐rich sulfide and other low‐temperature minerals reveal at least three episodic‐alteration events on the parent body of CM chondrites (1) formation of P‐O‐rich sulfide during sulfur‐rich aqueous alteration of P‐rich FeNi metal, (2) formation of Ca‐carbonate during local carbonation, and (3) alteration of P‐O‐rich sulfide and formation of tochilinite during a period of late‐stage intensive aqueous alteration.     

Primordial and cosmogenic noble gases in the Sutter's Mill CM chondrite

The Sutter's Mill (SM) CM chondrite fell in California in 2012. The CM chondrite group is one of the most primitive, consisting of unequilibrated minerals, but some of them have experienced complex processes occurring on their parent body, such as aqueous alteration, thermal metamorphism, brecciation, and solar wind implantation. We have determined noble gas concentrations and isotopic compositions for SM samples using a stepped heating gas extraction method, in addition to mineralogical observation of the specimens. The primordial noble gas abundances, especially the P3 component trapped in presolar diamonds, confirm the classification of SM as a CM chondrite. The mineralogical features of SM indicate that it experienced mild thermal alteration after aqueous alteration. The heating temperature is estimated to be <350 °C based on the release profile of primordial ³⁶Ar. The presence of a Ni‐rich Fe‐Ni metal suggests that a minor part of SM has experienced heating at >500 °C. The variation in the heating temperature of thermal alteration is consistent with the texture as a breccia. The heterogeneous distribution of solar wind noble gases is also consistent with it. The cosmic‐ray exposure (CRE) age for SM is calculated to be 0.059 ± 0.023 Myr based on cosmogenic ²¹Ne by considering trapped noble gases as solar wind, the terrestrial atmosphere, P1 (or Q), P3, A2, and G components. The CRE age lies at the shorter end of the CRE age distribution of the CM chondrite group.     

Sulfur isotopic composition of Fe‐Ni sulfide grains in CI and CM carbonaceous chondrites

Abstract– In situ secondary ion mass spectrometry analyses of ³²S, ³³S, and ³⁴S in iron‐nickel sulfide grains in two CI1 chondrites and six CM chondrites were performed. The results show a wider range of both enrichment and depletion in δ³⁴S relative to troilite from the Canyon Diablo meteorite (CDT) than has been observed in previous studies. All data points lie within error of a single mass dependent fractionation line. Sulfides from CI1 chondrites show δ³⁴S_CDT from ?0.7 to 6.8‰, while sulfide grains in the CM1 chondrite are generally depleted in heavy sulfur relative to CDT (δ³⁴S from ?2.9 to 1.8‰). CM2 chondrites contain sulfide grains that show enrichment and depletion in ³⁴S (δ³⁴S_CDT from ?7.0 to 6.8‰). Sulfates forming from sulfide grains during aqueous alteration on the chondrite parent body are suggested to concentrate light sulfur, leaving the remaining sulfide grains enriched in the heavy isotopes of sulfur. The average degree of enrichment in ³⁴S in CM chondrite sulfides is broadly consistent with previously suggested alteration sequences.     

The formation of Ca‐, Fe‐rich silicates in reduced and oxidized CV chondrites: The roles of impact‐modified porosity and permeability,and heterogeneous distribution of water ices

CV (Vigarano type) carbonaceous chondrites, comprising Allende‐like (CV_oxA) and Bali‐like (CV_oxB) oxidized and reduced (CV_red) subgroups, experienced differing degrees of fluid‐assisted thermal and shock metamorphism. The abundance and speciation of secondary minerals produced during asteroidal alteration differ among the subgroups: (1) ferroan olivine and diopside–hedenbergite solid solution pyroxenes are common in all CVs; (2) nepheline and sodalite are abundant in CV_oxA, rare in CV_red, and absent in CV_oxB; (3) phyllosilicates and nearly pure fayalite are common in CV_oxB, rare in CV_red, and virtually absent in CV_oxA; (4) andradite, magnetite, and Fe‐Ni‐sulfides are common in oxidized CVs, but rare in reduced CVs; the latter contain kirschsteinite instead. Thus, a previously unrecognized correlation exists between meteorite bulk permeabilities and porosities with the speciation of the Ca‐, Fe‐rich silicates (pyroxenes, andradite, kirschsteinite) among the CVox and CVred meteorites. The extent of secondary mineralization was controlled by the distribution of water ices, permeability, and porosity, which in turn were controlled by impacts on the asteroidal parent body. More intense shock metamorphism in the region where the reduced CVs originated decreased their porosity and permeability while simultaneously expelling intergranular ices and fluids. The mineralogy, petrography, and bulk chemical compositions of both the reduced and oxidized CV chondrites indicate that mobile elements were redistributed between Ca,Al‐rich inclusions, dark inclusions, chondrules, and matrices only locally; there is no evidence for large‐scale (>several cm) fluid transport. Published ⁵³Mn‐⁵³Cr ages of secondary fayalite in CV, CO, and unequilibrated ordinary chondrites, and carbonates in CI, CM, and CR chondrites are consistent with aqueous alteration initiated by heating of water ice‐bearing asteroids by decay of ²⁶Al, not shock metamorphism.     

Sutter's Mill dicarboxylic acids as possible tracers of parent‐body alteration processes

Dicarboxylic acids were searched for in three Sutter's Mill (SM) fragments (SM2 collected prerain, SM12, and SM41) and found to occur almost exclusively as linear species of 3‐ to 14‐carbon long. Between these, concentrations were low, with measured quantities typically less than 10 nmole g^?1 of meteorite and a maximum of 6.8 nmole g^?1 of meteorite for suberic acid in SM12. The SM acids' molecular distribution is consistent with a nonbiological origin and differs from those of CMs, such as Murchison or Murray, and of some stones of the C2‐ungrouped Tagish Lake meteorite, where they are abundant and varied. Powder X‐ray diffraction of SM12 and SM41 show them to be dominated by clays/amorphous material, with lesser amounts of Fe‐sulfides, magnetite, and calcite. Thermal gravimetric (TG) analysis shows mass losses up to 1000 °C of 11.4% (SM12) and 9.4% (SM41). These losses are low compared with other clay‐rich carbonaceous chondrites, such as Murchison (14.5%) and Orgueil (21.1%). The TG data are indicative of partially dehydrated clays, in accordance with published work on SM2, for which mineralogical studies suggest asteroidal heating to around 500 °C. In view of these compositional traits and mineralogical features, it is suggested that the dicarboxylic acids observed in the SM fragments we analyzed likely represent a combination of molecular species original to the meteorite as well as secondary products formed during parent‐body alteration processes, such as asteroidal heating.