CM Chondrites Research Articles

Hydrogen isotopic evidence for nebular pre-hydration and the limited role of parent-body processes in CM chondrites

The conditions and environments in which hydrated phases in unequilibrated meteorites formed remain debated. Among carbonaceous chondrites, Mighei-type chondrites (CMs) display a large range in the degree of aqueous alteration, and thus record different stages of hydration and alteration. Here, we report the bulk H, C, and N contents, H and C isotopic compositions, and thermogravimetric signatures of the most- and least-altered CMs known so far, Kolang and Asuka 12236, respectively. We also report in-situ SIMS measurements of the hydrogen isotopic compositions of water in both chondrites. Compared to other CMs, Asuka 12236 has the lowest bulk water content (3.3 wt.% H2O) and the most D-rich water and bulk isotopic compositions (δD = 180‰ and 280‰, respectively). Combined with literature data, our results show that phyllosilicate-bearing CMs altered to varying degrees accreted water-ice grains with similar isotopic compositions. These results demonstrate that the hydrogen isotopic variations in CM chondrites (i) are not controlled by secondary alteration processes and (ii) were mostly shaped by interactions between the protoplanetary disk and the molecular cloud that episodically fed the disk over several million years. The minimally altered CM chondrites Paris and Asuka 12236 display peculiar, D-rich, hydrogen isotopic compositions that imply the presence of another H-bearing component in addition to insoluble organic matter and phyllosilicates. This component is most likely the hydrated amorphous silicates that are ubiquitous in these chondrites. CM bulk H and O isotopic compositions are linearly correlated, implying that (i) amorphous silicates in CM matrices were already hydrated by disk processes before the onset of CM parent-body alteration, and (ii) the quest for a hypothetically water-free CM3 is illusory.

Titanium and chromium isotopic compositions of calcium-aluminum-rich inclusions: Implications for the sources of isotopic anomalies and the formation of distinct isotopic reservoirs in the early Solar System

As the earliest-dated solids in our Solar System, calcium-aluminum-rich inclusions (CAIs) provide a record of their formation environment near the young Sun and hold clues to the formation of planetary-scale isotopic reservoirs in the solar protoplanetary disk. Although CAIs from several CV, CK, CM, CO, and ordinary chondrites have been analyzed previously for their Ti isotopic compositions, CAIs from just three CV chondrites have been analyzed for their Cr isotopic compositions, and only a handful of CAIs have been measured for both their Ti and Cr isotopic compositions. We report mass-independent Ti and Cr isotopic anomalies in several CAIs from CV and CK chondrites; this is the first report of the Cr isotopic composition of a CAI from a CK chondrite. With these additional data, we aim to better constrain the compositional range of CAIs in ε50Ti versus ε54Cr space, thereby facilitating the isotopic characterization of the material inherited by the solar protoplanetary disk and the role of CAIs in the formation of distinct planetary-scale isotopic reservoirs in our early Solar System. The narrow range in isotopic anomalies in CAIs when compared to other early-formed refractory inclusions such as platy hibonite crystals (PLACs) and spinel-hibonite inclusions (SHIBs) suggests that CAIs record the mixing of these precursor materials and the averaging of their larger isotopic anomalies. The isotopic composition of CAIs is therefore likely the result of a combination of factors, including mixing of material inherited from their formation region, heterogeneous carrier phase distribution, and thermal processing in the disk. The ε50Ti and ε54Cr isotopic compositions of CAIs are not correlated, further demonstrating that these isotopic anomalies have different carrier phases. The Ti and Cr isotopic compositions of CAIs additionally show that CAIs alone cannot be responsible for the compositional difference between the non-carbonaceous chondritic (NC) and carbonaceous chondritic (CC) isotopic reservoirs but nevertheless do play a role in the formation of these large-scale isotopic reservoirs in the early Solar System.

Spectral and mineralogical effects of heating on CM chondrite and related asteroids

Several carbonaceous chondrites (CCs) display evidence of aqueous and thermal alteration. However, the process of thermal alteration is not fully understood. To investigate the spectral variations caused by thermal alteration, we heated powders of CM2 CCs Murchison and Jbilet Winselwan, as well as a simulant Murchison mixture (WMM) and its end members. Heating was conducted up to 1200 °C, in 100 °C increments under a purified nitrogen environment. We also compared the findings of our study with results of previous heating experiments conducted on CCs to better understand the effect differing conditions have on the spectral properties observed. Formation of Fe3+ oxyhydroxides and the decomposition of serpentine due to heating are confirmed by both reflectance and X-ray diffraction (XRD) data. Fe3+ oxyhydroxides features such as a steep slope in between 350 to ∼700 nm, and an ∼850 nm feature can be seen starting at ∼300 and 400 °C, respectively. The serpentine-associated features start to decompose at ∼700 °C and disappear by ∼900 °C. Spectra >1000 °C are generally dark and featureless and above this temperature, mafic silicate absorption bands begin to appear. Our results show that heating-induced spectral variations are evident, and the nature of these changes depends on various parameters including temperature, experimental conditions, duration of heating, sample grain size, as well as mineralogical changes accompanying heating, and heterogeneity between CCs.

Recovery and curation of the Winchcombe (CM2) meteorite

AbstractThe Winchcombe meteorite fell on February 28, 2021 and was the first recovered meteorite fall in the UK for 30 years, and the first UK carbonaceous chondrite. The meteorite was widely observed by meteor camera networks, doorbell cameras, and eyewitnesses, and 213.5 g (around 35% of the final recovered mass) was collected quickly—within 12 h—of its fall. It, therefore, represents an opportunity to study very pristine extra‐terrestrial material and requires appropriate careful curation. The meteorite fell in a narrow (600 m across) strewn field ~8.5 km long and oriented approximately east–west, with the largest single fragment at the farthest (east) end in the town of Winchcombe, Gloucestershire. Of the total known mass of 602 g, around 525 g is curated at the Natural History Museum, London. A sample analysis plan was devised within a month of the fall to enable scientists in the UK and beyond to quickly access and analyze fresh material. The sample is stored long term in a nitrogen atmosphere glove box. Preliminary macroscopic and electron microscopic examinations show it to be a CM2 chondrite, and despite an early search, no fragile minerals, such as halite, sulfur, etc., were observed.

Insoluble macromolecular organic matter in the Winchcombe meteorite

AbstractThe Winchcombe meteorite fell on February 28, 2021 in Gloucestershire, United Kingdom. As the most accurately recorded carbonaceous chondrite fall, the Winchcombe meteorite represents an opportunity to link a tangible sample of known chemical constitution to a specific region of the solar system whose chemistry can only be otherwise predicted or observed remotely. Winchcombe is a CM carbonaceous chondrite, a group known for their rich and varied abiotic organic chemistry. The rapid collection of Winchcombe provides an opportunity to study a relatively terrestrial contaminant‐limited meteoritic organic assemblage. The majority of the organic matter in CM chondrites is macromolecular in nature and we have performed nondestructive and destructive analyses of Winchcombe by Raman spectroscopy, online pyrolysis–gas chromatography–mass spectrometry (pyrolysis–GC–MS), and stepped combustion. The Winchcombe pyrolysis products were consistent with a CM chondrite, namely aromatic and polycyclic aromatic hydrocarbons, sulfur‐containing units including thiophenes, oxygen‐containing units such as phenols and furans, and nitrogen‐containing units such as pyridine; many substituted/alkylated forms of these units were also present. The presence of phenols in the online pyrolysis products indicated only limited influence from aqueous alteration, which can deplete the phenol precursors in the macromolecule when aqueous alteration is extensive. Raman spectroscopy and stepped combustion also generated responses consistent with a CM chondrite. The pyrolysis–GC–MS data are likely to reflect the more labile and thermally sensitive portions of the macromolecular materials while the Raman and stepped combustion data will also reflect the more refractory and nonpyrolyzable component; hence, we accessed the complete macromolecular fraction of the recently fallen Winchcombe meteorite and revealed a chemical constitution that is similar to other meteorites of the CM group.

Winchcombe: An example of rapid terrestrial alteration of a CM chondrite

AbstractWinchcombe is a CM chondrite that fell in England on February 28, 2021. Its rapid retrieval was well characterized. Within two polished sections of Winchcombe, terrestrial phases were observed. Calcite and calcium sulfates were found in a sample recovered from a field on March 6, 2021, and halite was observed on a sample months after its recovery from a driveway on March 2, 2021. These terrestrial phases were characterized by scanning electron microscopy, Raman spectroscopy, and transmission electron microscopy. Calcite veins crosscut the fusion crust and therefore postdate it. The calcite likely precipitated in the damp environment (sheep field) where the meteorite lay for six days prior to its retrieval. The sulfates occur on the edges of the sample and were identified as three minerals: gypsum, bassanite, and anhydrite. Given that the sulfates occur only on the sample's edges, including on top of the fusion crust, they formed after Winchcombe fell. Sulfate precipitation is attributed to the damp fall environment, likely resulted from sulfide‐derived H2S reacting with calcite within the meteorite. Halite occurs as euhedral crystals only on the surface of a polished section and exclusively in areas relatively enriched in sodium. It was likely produced by the interaction of the polished rock slice with the humid laboratory air over a period of months. The sulfates, fusion crust calcite, and halite all post‐date Winchcombe's entry into the Earth's atmosphere and showcase how rapidly meteorite falls can be terrestrially altered.

New Constraints for Supernova Models from Presolar Silicon Carbide X Grains with Very High 26Al/27Al Ratios

We report C, N, Mg-Al, Si, and S isotope data of six 1–3 μm-sized SiC grains of Type X from the Murchison CM2 chondrite, believed to have formed in the ejecta of core-collapse supernova (CCSN) explosions. Their C, N, and Si isotopic compositions are fully compatible with previously studied X grains. Magnesium is essentially monoisotopic 26Mg which gives clear evidence for the decay of radioactive 26Al. Inferred initial 26Al/27Al ratios are between 0.6 and 0.78 which is at the upper end of previously observed ratios of X grains. Contamination with terrestrial or solar system Al apparently is low or absent, which makes the X grains from this study particularly interesting and useful for a quantitative comparison of Al isotope data with predictions from supernova models. The consistently high 26Al/27Al ratios observed here may suggest that the lower 26Al/27Al ratios of many X grains from the literature are the result of significant Al contamination and in part also of an improper quantification of 26Al. The real dispersion of 26Al/27Al ratios in X grains needs to be explored by future studies. The high observed 26Al/27Al ratios in this work provide a crucial constraint for the production of 26Al in CCSN models. We explored different CCSN models, including both “classical” and H ingestion CCSN models. It is found that the classical models cannot account for the high 26Al/27Al ratios observed here; in contrast, H ingestion models are able to reproduce the 26Al/27Al ratios along with C, N, and Si isotopic ratios reasonably well.

Assessing the spatial variability of the ~3 μm OH/H2O absorption feature in CM2 carbonaceous chondrites

AbstractH2O and OH are readily detected in hydrated minerals in CM chondrites via reflectance spectroscopy due to their characteristic vibration absorptions at infrared wavelengths. Previous spectroscopic work on bulk powdered CM chondrites has shown that spectral parameters, like the wavelength position of the “3 μm absorption feature,” vary systematically with the extent to which the samples have been aqueously altered. However, it is yet unclear how these spectral features may vary across an intact meteorite chip when measured at spatial scales smaller than that of the individual components of the meteorite. Here, we explore the spatial variability of this spectral feature and others on intact CM2 chips which, unlike powders, retain their petrologic and textural characteristics. We also model the modal mineralogy of the bulk meteorite powders and correlate this with key spectral features, demonstrating that microscope Fourier transform infrared spectroscopic mapping provides a powerful, rapid, and non‐destructive technique for assessing compositional diversity and variations in water–rock interactions in chondritic planetary materials. In all CM2 chondrites studied here, we find that variations in the position, shape, and strength of the 3 μm absorption feature reveal a single chondrite can exhibit as much spectral variation as the entire suite of CM2 chondrites. The observed variations in the position and shape of the 3 μm feature within individual CM2 chondrite chips suggest a range of alteration products (e.g., Mg‐rich to Fe‐rich phyllosilicates) are present and record sub‐mm scale variations in the amount and/or chemistry of the altering fluids. The samples having experienced the most progressive aqueous alteration show the least amount of variability in features like the 3 μm absorption band minimum position, whereas the least altered samples exhibit the most variability. We also find that the bulk spectral signatures in the least altered samples appear to be biased toward the spectral signatures of clasts versus matrix. By extension, asteroid reflectance spectra exhibiting 3 μm absorption features consistent with those measured here may be interpreted in a similar framework in which the spectrum of what may appear to be the least altered asteroids represents an average that belies the true diversity of mineralogy and chemistry of the body.

The amino acid and polycyclic aromatic hydrocarbon compositions of the promptly recovered CM2 Winchcombe carbonaceous chondrite

AbstractThe rapid recovery of the Winchcombe meteorite offers a valuable opportunity to study the soluble organic matter (SOM) profile in pristine carbonaceous astromaterials. Our interests in the biologically relevant molecules, amino acids—monomers of protein, and the most prevalent meteoritic organics—polycyclic aromatic hydrocarbons (PAHs) are addressed by analyzing the solvent extracts of a Winchcombe meteorite stone using gas chromatography mass spectrometry. The Winchcombe sample contains an amino acid abundance of ~1132 parts‐per‐billion that is about 10 times lower than other CM2 meteorites. The detection of terrestrially rare amino acids, including α‐aminoisobutyric acid (AIB); isovaline; β‐alanine; α‐, β‐, and γ‐amino‐n‐butyric acids; and 5‐aminopentanoic acid, and the racemic enantiomeric ratios (D/L = 1) observed for alanine and isovaline indicate that these amino acids are indigenous to the meteorite and not terrestrial contaminants. The presence of predominantly α‐AIB and isovaline is consistent with their formation via the Strecker‐cyanohydrin synthetic pathway. The L‐enantiomeric excesses in isovaline previously observed for aqueously altered meteorites were viewed as an indicator of parent body aqueous processing; thus, the racemic ratio of isovaline observed for Winchcombe, alongside the overall high free:total amino acid ratio, and the low amino acid concentration suggest that the analyzed stone is derived from a lithology that has experienced brief episode(s) of aqueous alteration. Winchcombe also contains 2‐ to 6‐ring alkylated and nonalkylated PAHs. The low total PAHs abundance (6177 ppb) and high nonalkylated:alkylated ratio are distinct from that observed for heavily aqueously altered CMs. The weak petrographic properties of Winchcombe, as well as the discrepancies observed for the Winchcombe SOM content—a low total amino acid abundance comparable to heavily altered CMs, and yet the high free:total amino acid and nonalkylated:alkylated PAH ratios are on par with the less altered CMs—suggest that Winchcombe could represent a class of weak, poorly lithified meteorite not been previously studied.

The fusion crust of the Winchcombe meteorite: A preserved record of atmospheric entry processes

AbstractFusion crusts form during the atmospheric entry heating of meteorites and preserve a record of the conditions that occurred during deceleration in the atmosphere. The fusion crust of the Winchcombe meteorite closely resembles that of other stony meteorites, and in particular CM2 chondrites, since it is dominated by olivine phenocrysts set in a glassy mesostasis with magnetite, and is highly vesicular. Dehydration cracks are unusually abundant in Winchcombe. Failure of this weak layer is an additional ablation mechanism to produce large numbers of particles during deceleration, consistent with the observation of pulses of plasma in videos of the Winchcombe fireball. Calving events might provide an observable phenomenon related to meteorites that are particularly susceptible to dehydration. Oscillatory zoning is observed within olivine phenocrysts in the fusion crust, in contrast to other meteorites, perhaps owing to temperature fluctuations resulting from calving events. Magnetite monolayers are found in the crust, and have also not been previously reported, and form discontinuous strata. These features grade into magnetite rims formed on the external surface of the crust and suggest the trapping of surface magnetite by collapse of melt. Magnetite monolayers may be a feature of meteorites that undergo significant degassing. Silicate warts with dendritic textures were observed and are suggested to be droplets ablated from another stone in the shower. They, therefore, represent the first evidence for intershower transfer of ablation materials and are consistent with the other evidence in the Winchcombe meteorite for unusually intense gas loss and ablation, despite its low entry velocity.

From whom Bells tolls: Reclassifying Bells among CR chondrites and implications for the formation conditions of CR parent bodies

AbstractThe ungrouped carbonaceous chondrite (CC) Bells has long been considered petrographically similar to CM chondrites based on its matrix abundance and degree of aqueous alteration, but also shows significant isotopic affinities to CR chondrites. Its taxonomic status is thus important for clarifying the relationship of the CRHB (formerly “CR”) clan with other CCs. In this study, we measured the oxygen isotopic compositions of olivines in type I chondrules and isolated olivine grains in Bells. Bells olivines mostly have ∆17O > −4‰, similar to CR chondrites but unlike other CCs that are rich in refractory inclusions, in which chondrules are generally richer in 16O. Therefore, Bells is a CR chondrite (albeit an anomalous one), most similar to the rare, matrix‐rich CRs like Al Rais. These chondrites (i) may not necessarily derive from the same primary parent body as mainstream CRs, (ii) bear witness to significant variations of the matrix/chondrule ratio within the CRHB clan, and (iii) may be a good analog for samples retrieved by the space mission OSIRIS‐REx.

The Winchcombe meteorite—A regolith breccia from a rubble pile CM chondrite asteroid

AbstractThe Winchcombe meteorite is a CM chondrite breccia composed of eight distinct lithological units plus a cataclastic matrix. The degree of aqueous alteration varies between intensely altered CM2.0 and moderately altered CM2.6. Although no lithology dominates, three heavily altered rock types (CM2.1–2.3) represent >70 area%. Tochilinite–cronstedtite intergrowths (TCIs) are common in several lithologies. Their compositions can vary significantly, even within a single lithology, which can prevent a clear assessment of alteration extent if only TCI composition is considered. We suggest that this is due to early alteration under localized geochemical microenvironments creating a diversity of compositions and because later reprocessing was incomplete, leaving a record of the parent body's fluid history. In Winchcombe, the fragments of primary accretionary rock are held within a cataclastic matrix (~15 area%). This material is impact‐derived fallback debris. Its grain size and texture suggest that the disruption of the original parent asteroid responded by intergranular fracture at grain sizes <100 μm, while larger phases, such as whole chondrules, splintered apart. Re‐accretion formed a poorly lithified body. During atmospheric entry, the Winchcombe meteoroid broke apart with new fractures preferentially cutting through the weaker cataclastic matrix and separating the breccia into its component clasts. The strength of the cataclastic matrix imparts a control on the survival of CM chondrite meteoroids. Winchcombe's unweathered state and diversity of lithologies make it an ideal sample for exploring the geological history of the CM chondrite group.

Three-dimensional imaging of high-velocity-impact induced crack growth in carbonaceous meteorites

The material strength of meteorites provides useful information on the make-up and history of asteroids. However, the unique determination of the material strength of a meteorite is difficult because of the wide range of strengths many meteorites exhibit. Even within a single sample, complicated textures and mineral granular compositions make measurements difficult. Michikami et al. (2019) investigated the impact-induced crack growth in ordinary (L5) chondrites and indicated that crack growth is largely affected by the strength of individual mineral grains (and/or chondrules). In this study, we examine the strengths of mineral grains in carbonaceous meteorites qualitatively. To this end, we use X-ray microtomography to investigate how chondrules are affected by impact-induced crack growth in carbonaceous meteorites. Spherical alumina projectiles with a diameter of 1.0 mm were fired into the surfaces of seven Allende (CV) meteorite target samples with sizes of ∼1 to 2 cm at a nominal impact velocity of 2.0 km/s. In addition, spherical glass projectiles with a diameter 0.8 mm were fired into the target surfaces of two Murchison (CM) and two Aguas Zarcas (CM) meteorite target samples with sizes of ∼2 cm at a nominal impact velocity of 4.0 km/s. The results show that most cracks in CV chondrites tend to grow along the boundary surfaces of the chondrules, while most chondrule-related cracks in CM samples grow regardless of the boundary surfaces of the chondrules. This suggests that crack growth is largely affected by the chondrules' strength as indicated by Michikami et al. (2019). The weaker the strength of chondrules, the more likely crack growth tends to occur regardless of chondrule boundaries. We found that the mesostasis of chondrules in CM meteorite Murchison (and likely Aguas Zarcas) has experienced aqueous alteration and the chondrules have become structurally weak as a whole. This indicates that impact-induced crack propagation in CM chondrites differs from thermal-fatigue induced crack propagation inferred from previous studies. As the sample material to be returned from asteroid Bennu is considered to be related to CM chondrites, we propose that observation of the cracks in chondrules in Bennu samples might tell us whether those cracks are impact- or thermal-fatigue-induced.

Shidian meteorite, a new fall analog of near‐Earth asteroid (101955) Bennu

AbstractShidian is a recent meteorite which fell in Yunnan province, China, on November 27, 2017, and has been classified as a CM2 chondrite. Petrography, mineralogy, oxygen and chromium isotopic composition, reflectance spectrum, and density studies of Shidian are reported in this study. Clasts with different aqueous alteration degree, two type 1 clasts with nontypical CM petrography, and one metamorphic clast are observed in Shidian. Mineralogically, Shidian main body consists of phyllosilicates (∼70 vol%), forsterite (∼13 vol%), fayalitic olivine, carbonates, sulfide, high‐Ca pyroxene, magnetite framboids, and Fe‐Ni metal. The average electron microprobe analysis (EMPA) analytical totals of phyllosilicates are 84.07 ± 1.75 wt%, with average FeO/SiO2of tochilinite–cronstedtite intergrowths (TCIs) in different clasts ranging from 1.18 to 3.29. The bulk geochemical composition is characterized by flat rare earth element pattern, and by depletion of highly volatile elements. The whole rock oxygen isotopic composition is −0.51 ± 0.73‰, 5.44 ± 1.01‰, and −3.38 ± 0.20‰ for δ17O, δ18O, and Δ17O, respectively, with bulk chromium isotopic composition as ε54Cr = 1.00 ± 0.11. The grain density, bulk density, and porosity are 2.758 ± 0.008 g cm−3, 2.500 ± 0.004 g cm−3, and 9.37 ± 0.59%, respectively. The reflectance spectrum shows “blue” (negative) continuum slope across the visible and near‐infrared range, with characteristic absorption features (such as 0.765, 0.923, and 1.160 μm for phyllosilicates). These characteristics indicate that Shidian is an unheated, brecciated CM chondrite and may be an analog of asteroid Bennu.

Mapping Phyllosilicates on the Asteroid Bennu Using Thermal Emission Spectra and Machine Learning Model Applications

AbstractBennu, the target of the OSIRIS‐REx mission, is an asteroid with compositions analogous to low petrologic type CI, CM, CR, and/or ungrouped carbonaceous chondrites. Asteroids like Bennu provide information about the building blocks of the early Solar System. Analysis of the mid‐infrared remote sensing data informs mineral quantification. We apply a phyllosilicate specific model, developed by Breitenfeld et al. (2021, https://doi.org/10.1029/2021je007035) that distinguishes between Mg and Fe serpentines, to Baseball Diamond 1 (BBD1), equatorial station 3 (EQ3), and touch‐and‐go OSIRIS‐REx thermal emission spectrometer data. The average total phyllosilicate predictions are 73 (BBD1) and 72 vol% (EQ3). We observe higher Fe‐cronstedtite and lower Mg‐rich serpentine content in the equatorial region of Bennu than average. Mid‐infrared spectral variability may be explained by sorting effects through mass movement.

The cadmium and zinc isotope compositions of the silicate Earth – Implications for terrestrial volatile accretion

Zinc and Cd isotope compositions are presented for a comprehensive suite of terrestrial rocks to constrain the extent of Zn and Cd isotope fractionation during igneous processes and better define the δ66Zn and δ114Cd values of the silicate Earth (the δ values denote per mille deviations of 66Zn/64Zn from JMC Lyon Zn and of 114Cd/110Cd from NIST SRM 3108 Cd). Analyses of spinel lherzolites provide a bulk silicate Earth (BSE) δ114CdBSE value of –0.06 ± 0.03 ‰ (2SD). For Zn, the peridotite data of the current and previous studies define a mean δ66ZnBSE = 0.20 ± 0.05 ‰ (2SD). Komatiite analyses of this and published investigations yield similar mean values, which suggests that the Zn and Cd isotope compositions of the mantle remained fairly constant since the Archean. Data for loess provide upper continental crust compositions of δ114Cd = 0.03 ± 0.10 ‰ and δ66Zn = 0.23 ± 0.07 ‰. The Zn isotope and abundance data for peridotites and oceanic basalts are in accord with the previous observation of a mantle array, with basalts having higher Zn concentrations and δ66Zn values than the peridotites. To a first order, this reflects slightly incompatible behaviour of Zn during mantle melting and melt differentiation with associated enrichment of heavy Zn isotopes in the melt phase. Cadmium is marginally more incompatible than Zn during igneous processes and the oceanic basalts also display a minor enrichment of heavy Cd isotopes relative to peridotites. However, secondary processes produce significant Cd isotope variability in both mantle melts and peridotites, obscuring the primary igneous array. The δ66ZnBSE estimates of this and previous studies resemble the Zn isotope compositions of CV and CO carbonaceous and some enstatite chondrites. In contrast, the BSE has a lower δ114CdBSE value than enstatite and carbonaceous chondrites. This implies that the Cd isotope composition of the BSE was either fractionated during accretion or that Earth’s Cd inventory was not exclusively acquired from material related to carbonaceous and enstatite chondrites. Importantly, delivery of Zn and Cd to the BSE solely by CI and CM chondrites is not in accord with the meteorite and terrestrial stable isotope data of these elements.

Detection of incipient aqueous alteration in carbonaceous chondrites

We discuss if the detection of aqueous alteration depends on the techniques that are used. We apply different methods to estimate the extent of aqueous alteration on four ungrouped carbonaceous chondrites showing limited aqueous alteration and thermal metamorphism: Chwichiya 002, El Médano (EM) 200, Northwest Africa (NWA) 12957 and NWA 11750, classified as C3 or C3.00-ung. The aim is to propose a reliable methodology to identify the most primitive chondrites. Chwichiya 002, NWA 11750 and NWA 12957 display very primitive matrices and could be amongst the most primitive chondrites currently known, similar to the least altered lithologies of the CM chondrites Paris (CM2.9) and Asuka (A) 12085 (CM2.8), A 12236 (CM2.9) and A 12169 (CM3.0). The structure of organic matter and Cr2O3 in ferroan olivines show that the four meteorites have been less heated than the least metamorphosed standard/reference type 3 chondrite, Semarkona (LL3.00), with Chwichiya 002, NWA 12957 and NWA 11750 similar to the CO3.0 s, Acfer 094 (C2-ung) and Paris meteorites. Chwichiya 002 and NWA 12957 show similar alteration phases and degree of alteration, with high abundances of amorphous material with embedded metal and sulfide, resembling Glass with Embedded Metal and Sulfide (GEMS)-like materials, and tochilinite-cronstedtite intergrowths (TCIs) as the major alteration phases. The matrix in NWA 11750 contains aggregates of nanoscale olivine crystals and abundant carbonates, observed as micrometer-sized carbonate veins surrounding chondrules, and as nanoscale carbonates mixed with the fine-grained materials. It also contains abundant grains of metal and a low abundance of phyllosilicates. El Medano 200 shows a high abundance of magnetite (∼10 vol%), nanoscale phyllosilicates, troilite, and organic matter. The variability of the secondary alteration phases in the meteorites suggests different alteration mechanisms, likely depending on both the starting composition of the meteorites and the composition of the fluids of alteration.Scanning and transmission electron microscopy (SEM and TEM) allow the identification of primitive phases and the composition and spatial distribution of the secondary phases. X-ray diffraction (XRD) can detect alteration products, including some amorphous phases, although this is limited by the small coherence domains of small TCIs and other phyllosilicates. Transmission infrared (IR) spectroscopy can detect phyllosilicate and carbonate, but is ineffective for the detection of amorphous phases, metal, or sulfide. Both matrix defocused electron microprobe analyses (EMPA) and thermogravimetric analysis (TGA) allow detection of hydrated minerals, such as phyllosilicates and carbonates, but are strongly influenced by the presence of organic matter and do not reflect the overall alteration state of a meteorite. We conclude that the assessment of the primitivity of a chondrite is highly technique dependent. We propose a combination of XRD and the Cr2O3 in ferroan olivines or Raman spectroscopy for a rapid characterization of the alteration state of a chondrite and the detection of the most primitive meteorites. Finally, the combination of XRD and TEM allows for the detection of all primary and secondary phases and represents an ideal methodology for the characterization and detailed study of primitive chondrites and the different types of incipient aqueous alteration.

Evidence for impact shock and regolith transportation on CM, CI, and CV chondrite parent asteroids

AbstractWe explore impact shock processing of the regolith of parent asteroids of carbonaceous chondrites, which has not been considered a major process for hydrous carbonaceous chondrites. We describe shock‐produced minerals and features found in brecciated CI, CM, and CV chondrites, including agglutinates, a glassy melt pod, a shock melt vein, and melted sulfides. We also reexamine cognate clasts present in the Vigarano CV3 chondrites which appear to derive from asteroid ponds and exhibit cross‐bedded dish structures.

Polycyclic aromatic hydrocarbons in carbonaceous chondrites can be used as tracers of both pre-accretion and secondary processes

Carbonaceous chondrites contain a diverse suite of more or less soluble compounds, including polycyclic aromatic hydrocarbons (PAHs). These compounds are structured around two or more fused benzene rings, and have shown to be detected in various astrophysical environments. The origin of PAHs in carbonaceous chondrites is debated: they may originate from the interstellar medium (ISM) and thus potentially carry information on accretion processes. Alternatively, they may have formed or transformed during secondary processes on parent bodies and thus carry information about aqueous alteration conditions. Here, we investigate the nature, quantity, and isotopic composition of free PAHs in three recently recovered CM chondrites having experienced substantial and distinct degrees of alteration: the CM2.2 Aguas Zarcas, the CM2.0 Mukundpura and the CM1/2 Kolang. All the CMs investigated contain PAHs, with sizes ranging from 2 (naphthalene) to 5 cycles (benzopyrene). The concentration of PAHs is not correlated to the degree of alteration and larger PAHs are also the most depleted in 13C, suggesting an interstellar origin. Yet, the abundance of alkylated PAHs appears correlated to the degree of alteration and all the extracted PAHs are D-depleted, pointing towards hydrogen exchange with water having occurred during aqueous alteration. These combined results suggest that PAHs in CCs likely carry information on both accretion and alteration processes.

TEM Analyses of Carbonates from CM Chondrites - Possible Impact Events Revealed by Pervasive Microstructural Features

An abstract is not available for this content so a preview has been provided. As you have access to this content, a full PDF is available via the ‘Save PDF’ action button.