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Using infrared (IR) spectroscopy of thin sections, we characterize the relative degree of aqueous alteration and subsequent heating of a suite of CM chondrites to document spectral indicators of these processes that can contextualize observations of carbonaceous asteroids. We find that the progressive aqueous alteration of CMs manifests in two spectral regions. The low-wavenumber region (1200–400 cm−1; 8–25 μm) records the increasing proportion of Mg-Fe phyllosilicates relative to anhydrous silicates as aqueous alteration proceeds, with a highly correlated shift of the Christiansen feature (CF) to lower wavenumber and the Si-O bending band minimum to higher wavenumber, and an increase in depth of the Mg-OH band (~625 cm−1). The strongest correlation (R2 = 0.90) with petrologic subtype is the distance between the CF and Si-O stretching band minimum, which predicts the petrologic subtype of the sample to within 0.1. The high-wavenumber region (4000–2500 cm−1, ≤3.33 μm) probes the variation in abundance and composition of Mg-Fe serpentine and tochilinite among the altered CMs. All moderately to highly altered CMs (≤2.3) have an OH/H2O (‘3 μm’) band emission maximum of 3690 cm−1 (2.71 μm) indicative of Mg-bearing serpentine, and mildly aqueously altered CMs (≥ 2.5) have a wider band with a complex shape that results from contributions of Fe-bearing serpentine and tochilinite. Among weakly heated CMs (Stage II; 300–500 °C), the low-wavenumber region exhibits spectral features resulting from the dehydration and dehydroxylation of phyllosilicates that include broadening of the Si-O stretching band and a shift of its minimum to lower wavenumber, and the disappearance of the Mg-OH band. The location of the Si-O bending band minimum appears to be unaffected by mild heating. Extensively heated CMs (Stage III+; > 500 °C) have a low-wavenumber region dominated by the spectral features of secondary, Fe-bearing olivine and low-Ca pyroxene and thus are readily distinguished from unheated and mildly heated CMs. The OH/H2O band of all heated CMs is broad and rounded with an emission peak at lower wavenumbers (≤3636 cm−1; ≥2.75 μm) than in unheated CMs. However, spectral and petrographic evidence suggests that our heated CMs have been compromised by terrestrial rehydration. Our study confirms that thermal metamorphism effects are concentrated within the matrix and suggests that the matrix of the CM WIS 91600 had a CI-like mineralogy prior to heating.

For many years it has been suggested that the carbonaceous material found in association with Fe/Ni metal and metal carbides in primitive bodies is linked to the Fischer–Tropsch reaction. This is especially true with chondritic-porous interplanetary dust particles, which are considered to have a cometary origin and are among some of the most primitive and least processed materials available for study. Another phenomenon which occurs under the same carburizing conditions as the Fischer–Tropsch reaction is called metal dusting and could be a possible pathway to forming some of the carbonaceous material found in primitive bodies. Metal dusting is a catastrophic corrosion of metal under these carburizing conditions that results in a porous mixture of carbonaceous material, metal, and metal carbides. In the case of pure iron, type I metal dusting results in the formation of a metastable iron carbide, typically cementite, Fe3C. While metal dusting has been studied industrially for over 50 years, it does not appear to have been applied to the formation of carbonaceous material in astrophysical settings. In this work, the general mechanism of metal dusting on iron is described and a thermodynamic analysis of the dusting phenomena applied to solar nebula conditions. Rate measurements are made with pure iron samples over the temperature range from 400°C to 950°C. In addition, the products from experimental runs at 500°C and 600°C are studied by transmission electron microscopy. Results show that iron carbide particles are formed with carbonaceous material consisting of poorly graphitized carbon.

A number of different classifications have been proposed for the CR chondrites; this study aims at reconciling these different schemes. Mineralogy-based classification has proved particularly challenging for weakly to moderately altered CRs because incipient mineral replacement and elemental mobilization arising from aqueous alteration only affected the most susceptible primary phases, which are generally located in the matrix. Secondary matrix phases are extremely fine-grained (generally sub-micron) and heterogeneously mixed with primary nebular materials. Compositional and isotopic classification parameters are fraught with confounding factors, such as terrestrial weathering, impact processes, and variable abundance of clasts from different regions of the CR parent body or from altogether different planetary bodies. Here, detailed TEM observations from eighteen FIB sections retrieved from the matrices of nine Antarctic CR chondrites (EET 96259, GRA 95229, GRO 95577, GRO 03116, LAP 02342, LAP 04516, LAP 04720, MIL 07525, and MIL 090001) are presented, representing a range of petrologic types. Amorphous Fe–Mg silicates are found to be the dominant phase in all but the most altered CR chondrite matrices, which still retain significant amounts of these amorphous materials. Amorphous Fe–Mg silicates are mixed with phyllosilicates at the nanometer scale. The ratio of amorphous Fe–Mg silicates to phyllosilicates decreases as: (1) the size of phyllosilicates, (2) abundance of magnetite, and (3) replacement of Fe–Ni sulfides increase. Carbonates are only abundant in the most altered CR chondrite, GRO 95577. Nanophase Fe–Ni metal and tochilinite are present small abundances in most CR matrices. Based on the presence, abundance and size of phyllosilicates with respect to amorphous Fe–Mg silicates, the sub-micron features of CR chondrites have been linked to existing classification sequences, and possible reasons for inconsistencies among classification schemes are discussed.

Bennu (101195), target of the Origins, Spectral Interpretation, Resource Identification, Security, Regolith Explorer (OSIRIS-REx) mission, is a type-B asteroid with abundant spectral evidence for hydrated silicates, low thermal inertia “boulders” and frequent bursts of particle emission. We suggest that Bennu’s parent body formed in the outer solar system before it was perturbed into the asteroid belt and then evolved into a near-Earth object. We show that this is consistent with models of planetesimal evolution. Bennu has many characteristics expected for a dormant comet, and could potentially contain a minimum of 1 wt.% adsorbed water if its gross mineralogy is consistent with the Orgueil meteorite. This is in addition to any ice or water contained within the hydrous minerals themselves. Based on this hypothesis, we predict the properties of the samples that will be returned to Earth by the OSIRIS-REx mission, including abundant phyllosilicate minerals, amorphous hydrated silicates and low-density, very high-porosity aggregates, already observed by the OSIRIS-REx instrument suite. We predict enrichments in D/H and 15N/14N, high C/Mg ratios (>∼7 wt%), and a greater range of organic compositions than found in meteorites, including an organic component poor in aromatics, and a more labile organic fraction. Ammonium salts, ranging from NH4Cl to ammonium–organic acid salts could carry much of the nitrogen in comets, yet only NH4CH3COO and heavier salts are sufficiently stable to be found in these returned samples. Water adsorbed onto highly porous grains should also be detected provided that the sample return capsule remains below 300 K during Earth return, and this water should be isotopically heavy.

The water-soluble organic compounds in carbonaceous chondrite meteorites constitute a record of the synthetic reactions occurring at the birth of the solar system and those taking place during parent body alteration and may have been important for the later origins and development of life on Earth. In this present work, we have developed a novel methodology for the simultaneous analysis of the molecular distribution, compound-specific δ(13)C and enantiomeric compositions of aliphatic monocarboxylic acids (MCA) extracted from the hot-water extracts of sixteen carbonaceous chondrites from CM, CR, CO, CV and CK groups. We observed high concentrations of meteoritic MCAs, with total carbon weight percentages which in some cases approached those of carbonates and insoluble organic matter. Moreover, we found that the concentration of MCAs in CR chondrites is higher than in the other meteorite groups, with acetic acid exhibiting the highest concentration in all samples. The abundance of MCAs decreased with increasing molecular weight and with increasing aqueous and/or thermal alteration experienced by the meteorite sample. The δ(13)C isotopic values of MCAs ranged from −52 to +27‰, and aside from an inverse relationship between δ(13)C value and carbon straight-chain length for C(3)-C(6) MCAs in Murchison, the (13)C-isotopic values did not correlate with the number of carbon atoms per molecule. We also observed racemic compositions of 2-methylbutanoic acid in CM and CR chondrites. We used this novel analytical protocol and collective data to shed new light on the prebiotic origins of chondritic MCAs.

Chondrite materials with varying abundances of volatile-bearing phases are expected at the destinations for the asteroid sample-return missions Hayabusa2 and OSIRIS-REx. The targets of the missions are 162173 (1999 JU3) Ryugu and 101955 (1999 RQ36) Bennu. Spectroscopic analyses of these asteroids suggest that their surface materials are related to types 1 and 2 carbonaceous chondrites. Some studies suggest that the parent bodies of these chondrites may have also experienced some thermal and/or shock metamorphism. The physical properties of boulders at asteroid surfaces and fine particles in asteroid regoliths are consequences of the diverse processes that fragmented them, mobilized them, and redeposited them in unique accumulations. Sample-return missions are likely to encounter a broad range of carbonaceous chondrite (CC)-like materials, to which aqueous alteration, thermal, and shock metamorphism imparted changes affecting their sub-micron- to meter-scale physical properties. Consequently, implementation of scale-dependent analytical techniques to the study of the chemical, physical, and geotechnical characteristics of these CC-like materials is fundamental to safe mission operations, sample selection, and return. However, most of the available knowledge for informing and formulating expectations about regolith processes, products, and properties on carbonaceous small bodies comes from missions that studied anhydrous (e.g., Itokawa studied by Hayabusa) and/or much larger asteroids (e.g., Vesta studied by Dawn). No previous mission is likely directly relevant to small ice-free carbonaceous NEOs 162173 Ryugu or 101955 Bennu, although the Rosetta Spaceraft performed a flyby of the large asteroid Lutetia which has variously been classified as M and C type (Patzold et al., 2011). Carbonaceous chondrites carry the best record of the history, distribution, and activity of water in the early solar system. Ordinary and Enstatite chondrites carry only partial records, but these are still critical to understanding the full story. We will describe the records of water-rock interactions on asteroids, as recorded in these meteorites, with particular emphasis on the timing, nature, settings, and fluid compositions. An integral part of this story is the rare, but fortunate, preservation of actual early solar system water as aqueous fluid inclusions.

There are many indicators that suggest that the differences between asteroids and comets may result from their evolution over several billion years, based on similar accretion processes in the primitive solar nebula rather than in fundamental differences in their accretional histories. Our goal is to review some of the various processes (e.g., headwind drag-induced radial drift, grain–grain collisional dynamics, thermal processing vs. accretion time, etc.) that would act to accrete or to modify the accreted materials as a function of the size of the object. We do not account for the migration of the giant planets on the populations of asteroids and comets as the consequences of the proposed mixing episodes would come much later. We will, however, discuss the potential implications of the formation of the terrestrial planets on the population of meteorite parent bodies in the inner solar system. These same processes do not seem to have been important in or beyond the giant planet region of the solar nebula.

The analysis of water-soluble organic compounds in meteorites provides valuable insights into the prebiotic synthesis of organic matter and the processes that occurred during the formation of the solar system. We investigated the concentration of aliphatic monoamines present in the hot acid-water extracts of the unaltered Antarctic carbonaceous chondrites DOM 08006 (CO3) and MIL 05013 (CO3), and the thermally altered meteorites Allende (CV3), LAP 02206 (CV3), GRA 06101 (CV3), ALH 85002 (CK4), and EET 92002 (CK5). We have also reviewed and assessed the petrologic characteristics of the meteorites studied here, to evaluate the effects of asteroidal processing on the abundance and molecular distributions of monoamines. The CO3, CV3, CK4, and CK5 meteorites studied here contain total concentrations of amines ranging from 1.2 to 4.0 nmol/g of meteorite; these amounts are one to three orders of magnitude below those observed in carbonaceous chondrites from the CI, CM and CR groups. The low amine abundances for CV and CK chondrites may be related to their extensive degree of thermal metamorphism and/or to their low original amine content. Although the CO3 meteorites DOM 08006 and MIL 05013 do not show signs of thermal and aqueous alteration, their monoamine contents are comparable to those observed in moderately/extensively thermally altered CV3, CK4, and CK5 carbonaceous chondrites. The low content of monoamines in pristine CO carbonaceous chondrites suggests that the initial amounts, and not asteroidal processes, play a dominant role in the content of monoamines in carbonaceous chondrites. The primary monoamines, methylamine, ethylamine and n-propylamine constitute the most abundant amines in the CO3, CV3, CK4, and CK5 meteorites studied here. Contrary to the predominance of n-ω-amino acid isomers in CO3 and thermally altered meteorites, there appears to be no preference for the larger n-α-amines.

We have studied the petrologic characteristics of sulfide-metal lodes, polymineralic Fe-Ni nodules, and opaque assemblages in the CR2 chondrite Graves Nunataks (GRA) 06100, one of the most altered CR chondrites. Unlike low petrologic type CR chondrites, alteration of metal appears to have played a central role in the formation of secondary minerals in GRA 06100. Differences in the mineralogy and chemical compositions of materials in GRA 06100 suggest that it experienced higher temperatures than other CR2 chondrites. Mineralogic features indicative of high temperature include: (1) exsolution of Ni-poor and Ni-rich metal from nebular kamacite; (2) formation of sulfides, oxides, and phosphates; (3) changes in the Co/Ni ratios; and (4) carbidization of Fe-Ni metal. The conspicuous absence of pentlandite may indicate that peak temperatures exceeded 600 °C. Opaques appear to have been affected by the action of aqueous fluids that resulted in the formation of abundant oxides, Fe-rich carbonates, including endmember ankerite, and the sulfide-silicate-phosphate scorzalite. We suggest that these materials formed via impact-driven metamorphism. Mineralogic features indicative of impact metamorphism include (1) the presence of sulfide-metal lodes; (2) the abundance of polymineralic opaque assemblages with mosaic-like textures; and (3) the presence of suessite. Initial shock metamorphism probably resulted in replacement of nebular Fe-Ni metal in chondrules and in matrix by Ni-rich, Co-rich Fe metal, Al-Ti-Cr-rich alloys, and Fe sulfides, while subsequent hydrothermal alteration produced accessory oxides, phosphates, and Fe carbonates. An extensive network of sulfide-metal veins permitted effective exchange of siderophile elements from pre-existing metal nodules with adjacent chondrules and matrix, resulting in unusually high Fe contents in these objects.

A metamorphosed, unshocked, chondritic clast, containing approximately equal volumes of matrix and chondrules, has been identified in the primitive CR3 chondrite QUE 99177. The most striking features of this clast are the presence of ferroan omphacitic pyroxenes, amphiboles (pargasite and pargasitic hornblende) and coarse-grained (up to 70 μm) graphite laths. The clast also contains relatively equilibrated FeO-rich olivine, low-Ca pyroxene, and sulfides (pentlandite and troilite). The clast’s matrix contains coarse, interlocking crystals. The chondrules are extensively recrystallized, contain no mesostasis or metal, and present poorly-defined boundaries. Based on its compositional and crystallographic features, omphacite appears to have formed at high pressures (>6 GPa). Amphibole formation probably postdated graphite formation and occurred by reaction of olivine, clinopyroxene, and omphacite in the presence of an oxidizing, Na-rich fluid at high temperatures (>700 °C). The absence of metal suggests that this fluid was also rich in S.

– We have experimentally produced nanophase sulfide compounds and magnetite embedded in Si-rich amorphous materials by flash-cooling of a gas stream. Similar assemblages are ubiquitous, and often dominant components of samples of impact-processed silica aerogel tiles and submicron grains from comet 81P/Wild 2 were retrieved by NASA’s Stardust mission. Although the texture and compositions of nanosulfide compounds have been reproduced experimentally, the mechanisms of formation of these minerals and their relationship with the surrounding amorphous materials have not been established. In this study, we present evidence that both of these materials may not only be produced through cooling of a superheated liquid but they may have also been formed simultaneously by flash-cooling and subsequent deposition of a gas dominated by Fe-S-SiO-O2. In a dust generator at the Goddard Space Flight Center, samples are produced by direct gas-phase condensation from gaseous precursors followed by deposition, which effectively isolates the effects of gas-phase reactions from the effects of melting and condensation. High-resolution transmission electron microscopy images and energy-dispersive spectroscopy analysis show that these experiments replicate key features of materials from type B and type C Stardust tracks, including textures, distribution of inclusions, nanophase size, and compositional diversity. We argue that gas-phase reactions may have played a significant role in the capture environment for nanophase materials. Our results are consistent with a potential progenitor assemblage of micron and submicron-sized sulfides and submicron silica-bearing phases, which are commonly observed in chondritic interplanetary dust particles and in the matrices of the most pristine chondritic meteorites.

– We have conducted scanning electron microscope (SEM) and transmission electron microscope (TEM) studies of a variety of occurrences of matrix in the reduced CV3 chondrite breccia Vigarano. Matrix, which occurs as clastic interchondrule material and finer-grained rims, is dominated by morphologically variable olivines that host submicron, hercynitic spinel, and carbonaceous inclusions. Clastic matrix and fine-grained rims show significant differences in their olivine morphologies, abundance, and composition of olivine inclusions, and characteristics of the carbonaceous matter. We suggest that these differences are the result of different degrees of alteration of clastic matrix and rims and are not due to variability in their precursor materials. Textural and compositional characteristics of olivine in the matrix are consistent with formation by growth, possibly from an amorphous precursor material during asteroidal metamorphism, in the presence of limited quantities of aqueous fluids. Spinel inclusions in olivine may be nebular condensates that acted as seeds for nucleation of olivine or may have formed during metamorphism and were subsequently overgrown by olivine. Carbonaceous material occurs as nanometer-sized inclusions within olivine in both fine-grained rims and clastic matrix, but is most abundant as 100–200 nm grains, interstitial to matrix olivines. Most carbonaceous material is amorphous, but poorly graphitized carbon (PGC) also occurs as a minor component in both olivine inclusions and interstitial C. The widespread occurrence of fine-grained amorphous carbon grains in the interstitial regions between olivine grains may preserve the distribution and grain size of nebular organic material. No clear textural relationships exist between carbonaceous grains and the other mineralogical components of Vigarano matrix that could help constrain the origin of the organic grains (i.e., evidence for Fischer-Tropsch-type reactions). Finally, there are considerable differences between matrix olivines in Vigarano in comparison with those in oxidized CV3 chondrites. In particular, the mineralogy and morphology of the matrix olivines and the nature, composition, and distribution of inclusions in the olivine grains are distinct. Based on these differences, we conclude that matrix in the oxidized CV3 chondrites could not have formed by thermal processing of Vigarano-like material.

The mineralogy and bulk compositions of the matrices of the CR chondrites MET 00426 and QUE 99177 have been studied using a combination of SEM, EPMA, and TEM techniques. The matrices of these two chondrites are texturally, chemically, and mineralogically similar and are characterized by significant FeO-enrichments with respect to other CR chondrite matrices, nearly flat refractory lithophile patterns, variable volatile element patterns, and a simple mineral assemblage dominated by amorphous silicate material and Fe,Ni sulfides. Fine-grained, crystalline silicate phases such as olivine and pyroxene appear to be extremely rare in the matrices of both meteorites. Instead, the mineralogy of matrices and fine-grained rims of both meteorites consists of abundant amorphous FeO-rich silicate material, containing nanoparticles of Fe,Ni sulfides (troilite, pyrrhotite, and pentlandite). Secondary alteration minerals that are characteristic of other CR chondrites (e.g., Renazzo and Al Rais), such as phyllosilicates, magnetite, and calcite are also rare. The texture and mineralogy of the matrices of MET 00426 and QUE 99177 share many features with matrices in the primitive carbonaceous chondrites ALH A77307 (CO3.0) and Acfer 094 (unique). These observations show that MET 00426 and QUE 99177 are very low petrologic type 3 chondrites that have escaped the effects of aqueous alteration, unlike other CR chondrites, which are typically classified as petrologic type 2. We suggest that these meteorites represent additional samples of highly primitive, but extremely rare carbonaceous chondrites of petrologic type 3.00, according to the classification scheme of Grossman and Brearley (2005). The highly pristine nature of MET 00426 and QUE 99177 provides important additional insights into the origins of fine-grained materials in carbonaceous chondrites. Based on our new observations, we infer that the amorphous silicate material and nanosulfide particles that dominate the matrices of these meteorites formed in the solar nebula by rapid condensation of material following high-temperature events, such as those that formed chondrules.

Studies of two separate stones of the CV3 chondrite Vigarano have revealed the presence of previously unreported occurrences of calcite. In the first stone, calcite occurs as thin veins in a type B CAI. In contrast, observations of the second stone, which was recovered one month after its fall, show three calcite occurrences: networks of veins, vesicle fillings in the fusion crust, and pseudomorphic replacement of augite associated with a porphyritic olivine chondrule. The most common occurrence is as veins ranging in thickness from

Prior to becoming chondritic meteorites, primordial solids were a poorly consolidated mix of mm-scale igneous inclusions (chondrules) and high-porosity sub-μm dust (matrix). We used high-resolution numerical simulations to track the effect of impact-induced compaction on these materials. Here we show that impact velocities as low as 1.5 km s−1 were capable of heating the matrix to >1,000 K, with pressure–temperature varying by >10 GPa and >1,000 K over ~100 μm. Chondrules were unaffected, acting as heat-sinks: matrix temperature excursions were brief. As impact-induced compaction was a primary and ubiquitous process, our new understanding of its effects requires that key aspects of the chondrite record be re-evaluated: palaeomagnetism, petrography and variability in shock level across meteorite groups. Our data suggest a lithification mechanism for meteorites, and provide a ‘speed limit’ constraint on major compressive impacts that is inconsistent with recent models of solar system orbital architecture that require an early, rapid phase of main-belt collisional evolution., Collisions between primordial planetesimals led to the formation of our asteroids and meteorites. Here, the authors use modelling to explore the compaction of planetsimals, tracking how pressure, temperature and porosity may have varied during the impacts, helping interpret early Solar System processes.