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

The 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.     

Water abundance in the Tagish Lake meteorite from TGA and IR spectroscopy: Evaluation of aqueous alteration

Here, we evaluate the extent of aqueous alteration among five pristine specimens of the ungrouped Tagish Lake carbonaceous chondrite (TL5b, TL11h, TL11i, TL4, and TL10a) using thermogravimetric analysis (TGA) and infrared (IR) transmission spectroscopy. Both TGA and IR spectroscopy have proven to be reliable methods for determining the extent of aqueous alteration among different carbonaceous chondrites, in particular the CM chondrites (e.g., Garenne et al. 2014), with which Tagish Lake shares some affinities. Using these two methods, our goal is to incorporate TL4 and TL10a into the known alteration sequence of TL5b < TL11h < TL11i (Herd et al. 2011; Blinova et al. 2014a). This study highlights the compositional variability of the Tagish Lake specimens, which we ascribe to its brecciated nature. Our TGA and IR spectroscopy results are congruent with the reported alteration sequence, allowing us to introduce the TL4 and TL10a specimens in the following order: TL4 < TL5b ≤ TL10a < TL 11h < TL11i. Notably, these two specimens appear to be similar to the least altered lithologies previously reported, and the alteration of Tagish Lake is similar to that experienced by lesser altered members of the CM chondrites (>CM1.6). Based on these findings, Tagish Lake could be considered a 1.6–2.0 ungrouped carbonaceous chondrite. Visible and near‐IR reflectance measurements of Tagish Lake were also acquired in this study to revisit the Tagish Lake parent body connection. While other studies have paired Tagish Lake with D‐ and T‐type asteroid parent bodies, the reflectance spectra acquired in this study are variable among the different Tagish Lake specimens in relation to their alteration sequences; results match with spectra characteristic of C‐, X‐, Xc‐, and D‐type asteroids. The heterogeneity of Tagish Lake coupled with its low albedo makes the parent body connection a challenge.     

Nature and degree of aqueous alteration in CM and CI carbonaceous chondrites

We investigated the petrologic, geochemical, and spectral parameters that relate to the type and degree of aqueous alteration in nine CM chondrites and one CI (Ivuna) carbonaceous chondrite. Our underlying hypothesis is that the position and shape of the 3 μm band is diagnostic of phyllosilicate mineralogy. We measured reflectance spectra of the chondrites under dry conditions (elevated temperatures) and vacuum (10^?8 to 10^?7 torr) to minimize adsorbed water and mimic the space environment, for subsequent comparison with reflectance spectra of asteroids. We have identified three spectral CM groups in addition to Ivuna. “Group 1,” the least altered group as determined from various alteration indices, is characterized by 3 μm band centers at longer wavelengths, and is consistent with cronstedtite (Fe‐serpentine). “Group 3,” the most altered group, is characterized by 3 μm band centers at shorter wavelengths and is consistent with antigorite (serpentine). “Group 2” is an intermediate group between group 1 and 3. Ivuna exhibits a unique spectrum that is distinct from the CM meteorites and is consistent with lizardite and chrysotile (serpentine). The petrologic and geochemical parameters, which were determined using electron microprobe analyses and microscopic observations, are found to be consistent with the three spectral groups. These results indicate that the distinct parent body aqueous alteration environments experienced by these carbonaceous chondrites can be distinguished using reflectance spectroscopy. High‐quality ground‐based telescopic observations of Main Belt asteroids can be expected to reveal not just whether an asteroid is hydrated, but also details of the alteration state.     

Absorption bands near three micrometers in diffuse reflectance spectra of carbonaceous chondrites: Comparison with asteroids

Abstract— We measured infrared diffuse reflectance spectra of several carbonaceous chondrites in order to obtain additional information on the surface materials of their presumed parent bodies, C-type asteroids. The presence and intensity of absorption bands near 3 μm in the reflectance spectra are due to the presence and abundance of hydrates and/or hydroxyl ions. The absorption features of the 3 μm hydration bands of carbonaceous chondrites were compared with those of asteroids 1 Ceres and 2 Pallas. They are commonly classified into separate subtypes, G- and B-type. The spectral shapes of Pallas and Renazzo (CR2 chondrite) around the 3 μm absorption band are an excellent match. This result may suggest that the amount of hydrous minerals in the surface material of Pallas is smaller than that in the CM2 or CI chondrites, and the hydrous minerals on the surface of Pallas may be similar to those found in Renazzo. The spectral features around the 3 μm band of Ceres are different from those of carbonaceous chondrites studied in this paper.     

Altered primary iron sulfides in CM2 and CR2 carbonaceous chondrites: Insights into parent body processes

The presence of primary iron sulfides that appear to be aqueously altered in CM and CR carbonaceous chondrites provides the potential to study the effects and, by extension, the conditions of aqueous alteration. In this work, we have used SEM, TEM, and EPMA techniques to characterize primary sulfides that show evidence of secondary alteration. The alteration styles consist of primary pyrrhotite altering to secondary pentlandite (CMs only), magnetite (CMs and CRs), and phyllosilicates (CMs only) in grains that initially formed by crystallization from immiscible sulfide melts in chondrules (pyrrhotite‐pentlandite intergrowth [PPI] grains). Textural, microstructural, and compositional data from altered sulfides in a suite of CM and CR chondrites have been used to constrain the conditions of alteration of these grains and determine their alteration mechanisms. This work shows that the PPI grains exhibit two styles of alteration—one to form porous pyrrhotite‐pentlandite (3P) grains by dissolution of precursor PPI grain pyrrhotite and subsequent secondary pentlandite precipitation (CMs only), and the other to form the altered PPI grains by pseudomorphic replacement of primary pyrrhotite by magnetite (CMs and CRs) or phyllosilicates (CMs only). The range of alteration textures and products is the result of differences in conditions of alteration due to the role of microchemical environments and/or brecciation. Our observations show that primary sulfides are sensitive indicators of aqueous alteration processes in CM and CR chondrites.     

Indigenous amino acids in primitive CR meteorites

Abstract— –CR chondrites are among the most primitive meteorites. In this paper, we report the first measurements of amino acids in Antarctic CR meteorites. Three CRs, Elephant Moraine (EET) 92042, Graves Nunataks (GRA) 95229, and Grosvenor Mountains (GRO) 95577, were analyzed for their amino acid content using high‐performance liquid chromatography with UV fluorescence detection (HPLC‐FD) and gas chromatography–mass spectrometry (GC‐MS). Our data show that EET 92042 and GRA 95229 are the most amino acid–rich chondrites ever analyzed, with total amino acid concentrations ranging from 180 ppm to 249 ppm. The most abundant amino acids present in the EET 92042 and GRA 95229 meteorites are the α‐amino acids glycine, isovaline, α‐aminoisobutyric acid (α‐AIB), and alanine, with δ¹³C values ranging from +31.6‰ to +50.5‰. The carbon isotope results together with racemic enantiomeric ratios determined for most amino acids strongly indicate an extraterrestrial origin for these compounds. Compared to Elephant Moraine (EET) 92042 and GRA 95229, the more aqueously altered GRO 95577 is depleted in amino acids. In both CRs and CMs, the absolute amino acid abundances appear to be related to the degree of aqueous alteration in their parent bodies. In addition, the relative abundances of α‐AIB and β‐alanine in the Antarctic CRs also appear to depend on the degree of aqueous alteration.     

Fine-grained chondrule rims in Mighei-like carbonaceous chondrites: Evidence for a nebular origin and modification by impacts and recurrent solar radiation heating

The Mighei-like carbonaceous (CM) chondrites, the most abundant carbonaceous chondrite group by number, further our understanding of processes that occurred in their formation region in the protoplanetary disk and in their parent body/bodies and provide analogs for understanding samples returned from carbonaceous asteroids. Chondrules in the CMs are commonly encircled by fine-grained rims (FGRs) whose origins are debated. We present the abundances, sizes, and petrographic observations of FGRs in six CMs that experienced varying intensities of parent body processing, including aqueous and thermal alteration. The samples studied here, in approximate order of increasing thermal alteration experienced, are Allan Hills 83100, Murchison, Meteorite Hills 01072, Elephant Moraine 96029, Yamato-793321, and Pecora Escarpment 91008. Based on observations of these CM chondrites, we recommend a new average apparent (2-D) chondrule diameter of 170 μm, which is smaller than previous estimates and overlaps with that of the Ornans-like carbonaceous (CO) chondrites. Thus, we suggest that chondrule diameters are not diagnostic for distinguishing between CM and CO chondrites. We also argue that chondrule foliation noted in ALH 83100, MET 01072, and Murchison resulted from multiple low-intensity impacts; that FGRs in CMs formed in the protoplanetary disk and were subsequently altered by both aqueous and thermal secondary alteration processes in their parent asteroid; and that the heat experienced by some CM chondrites may have originated from solar radiation of their source body/bodies during close solar passage as evidenced by the presence of evolved desiccation cracks in FGRs that formed by recurrent wetting and desiccation cycles.     

Linking mineralogy and spectroscopy of highly aqueously altered CM and CI carbonaceous chondrites in preparation for primitive asteroid sample return

The highly hydrated, petrologic type 1 CM and CI carbonaceous chondrites likely derived from primitive, water‐rich asteroids, two of which are the targets for JAXA's Hayabusa2 and NASA's OSIRIS‐REx missions. We have collected visible and near‐infrared (VNIR) and mid infrared (MIR) reflectance spectra from well‐characterized CM1/2, CM1, and CI1 chondrites and identified trends related to their mineralogy and degree of secondary processing. The spectral slope between 0.65 and 1.05 μm decreases with increasing total phyllosilicate abundance and increasing magnetite abundance, both of which are associated with more extensive aqueous alteration. Furthermore, features at ~3 μm shift from centers near 2.80 μm in the intermediately altered CM1/2 chondrites to near 2.73 μm in the highly altered CM1 chondrites. The Christiansen features (CF) and the transparency features shift to shorter wavelengths as the phyllosilicate composition of the meteorites becomes more Mg‐rich, which occurs as aqueous alteration proceeds. Spectra also show a feature near 6 μm, which is related to the presence of phyllosilicates, but is not a reliable parameter for estimating the degree of aqueous alteration. The observed trends can be used to estimate the surface mineralogy and the degree of aqueous alteration in remote observations of asteroids. For example, (1) Ceres has a sharp feature near 2.72 μm, which is similar in both position and shape to the same feature in the spectra of the highly altered CM1 MIL 05137, suggesting abundant Mg‐rich phyllosilicates on the surface. Notably, both OSIRIS‐REx and Hayabusa2 have onboard instruments which cover the VNIR and MIR wavelength ranges, so the results presented here will help in corroborating initial results from Bennu and Ryugu.     

Aqueous alteration of carbonaceous chondrites: Evidence for preaccretionary alteration—A review

Abstract— In most groups of carbonaceous chondrites, minerals occur that are formed due to aqueous alteration in the nebula and/or within meteorite parent bodies. For determining the evolution of materials in the early solar system, it is of significant importance to clearly identify evidence for either nebular or planetary aqueous alteration. Therefore, results from the study of chondrites have fundamental implications for ideas concerning nebular dynamics, gas-solid interactions in the nebula, and accretionary processes. Considering the topic of this review, it is important to define nebular and parent body processes. The solar nebula activity should include condensation processes of high- and low-temperature components as well as processes of chemical fractionation and grain-size sorting, mixing of solids and gas, and interactions between early formed solids with the remaining gas; but it should exclude processes that occurred in small uncompacted protoplanetary objects that may have been totally destroyed again before accretion of the final meteorite parent bodies. Therefore, the term “preaccretionary” instead of “nebula” is used in this paper to include all these processes that may have occurred in small precursor planetesimals. Currently, there is no doubt that parent body aqueous alteration is a fundamental process in the evolution of several groups of carbonaceous chondrites. However, due to textural and mineralogical observations and chemical analyses, strong arguments have been found also indicating preaccretionary aqueous alteration of distinct components in carbonaceous chondrites. In this paper, evidence for preaccretionary aqueous alteration in carbonaceous chondrites and their components taken from previous studies is discussed in detail. The strongest evidence for preaccretionary alteration comes from studies of CM chondrites. The survival of highly unequilibrated mineral assemblages in accretionary rims, and sharp contacts between chondrule glass and surrounding phyllosilicates, are only two important arguments for preaccretionary alteration features among many others discussed in the paper. Similar observations were also made in CR, CH and related chondrites. Due to the small abundance of water-bearing phases in CO and CV chondrites, the origin of phyllosilicates in these groups is less clear. A preaccretionary origin of hydrous phases in Ca-Al-rich inclusions (CAIs) has also been suggested by several scientists. In CI chondrites, no strong indications for such processes have been found, mainly due to heavy brecciation and severe parent body alteration.     

Elemental,isotopic, and structural changes in Tagish Lake insoluble organic matter produced by parent body processes

Here, we present the results of a multitechnique study of the bulk properties of insoluble organic material (IOM) from the Tagish Lake meteorite, including four lithologies that have undergone different degrees of aqueous alteration. The IOM C contents of all four lithologies are very uniform and comprise about half the bulk C and N contents of the lithologies. However, the bulk IOM elemental and isotopic compositions vary significantly. In particular, there is a correlated decrease in bulk IOM H/C ratios and δD values with increasing degree of alteration—the IOM in the least altered lithology is intermediate between CM and CR IOM, while that in the more altered lithologies resembles the very aromatic IOM in mildly metamorphosed CV and CO chondrites, and heated CMs. Nuclear magnetic resonance (NMR) spectroscopy, C X‐ray absorption near‐edge (XANES), and Fourier transform infrared (FTIR) spectroscopy confirm and quantitate this transformation from CR‐like, relatively aliphatic IOM functional group chemistry to a highly aromatic one. The transformation is almost certainly thermally driven, and probably occurred under hydrothermal conditions. The lack of a paramagnetic shift in ¹³C NMR spectra and 1s‐σ* exciton in the C‐XANES spectra, both typically seen in metamorphosed chondrites, shows that the temperatures were lower and/or the timescales were shorter than experienced by even the least metamorphosed type 3 chondrites. Two endmember models were considered to quantitatively account for the changes in IOM functional group chemistry, but the one in which the transformations involved quantitative conversion of aliphatic material to aromatic material was the more successful. It seems likely that similar processes were involved in producing the diversity of IOM compositions and functional group chemistries among CR, CM, and CI chondrites. If correct, CRs experienced the lowest temperatures, while CM and CI chondrites experienced similar more elevated temperatures. This ordering is inconsistent with alteration temperatures based on mineralogy and O isotopes.     

The oxygen isotopic composition of water from Tagish Lake: Its relationship to low‐temperature phases and to other carbonaceous chondrites

Abstract— The fall and recovery of the Tagish Lake meteorite in British Columbia in January 2000 provided a unique opportunity to study relatively pristine samples of carbonaceous chondrite material. Measurements of the oxygen isotopic composition of water extracted under stepped pyrolysis from a bulk sample of this meteorite have allowed us to make comparisons with similar data obtained from CI and CM chondrites and so further investigate any relationships that may exist between these meteorites. The much lower yield of water bearing a terrestrial signature in Tagish Lake is indicative of the pristine nature of the meteorite. The relationship between the isotopic composition of this water and reported isotopic values for carbonates, bulk matrix and whole rock have been used to infer the extent and conditions under which parent‐body aqueous alteration occurred. In Tagish Lake the difference in Δ17O isotopic composition between the water and other phases is greater than that found in either CM or CI chondrites suggesting that reaction and isotopic exchange between components was more limited. This in turn suggests that in the case of Tagish Lake conditions during the processes of aqueous alteration on the parent body, which ultimately controlled the formation of new minerals, were distinct from those on both CI and CM parent bodies.     

Type 1 aqueous alteration in CM carbonaceous chondrites: Implications for the evolution of water‐rich asteroids

The CM carbonaceous chondrite meteorites experienced aqueous alteration in the early solar system. They range from mildly altered type 2 to almost completely hydrated type 1 chondrites, and offer a record of geochemical conditions on water‐rich asteroids. We show that CM1 chondrites contain abundant (84–91 vol%) phyllosilicate, plus olivine (4–8 vol%), magnetite (2–3 vol%), Fe‐sulfide (<5 vol%), and calcite (<2 vol%). The CM1/2 chondrites contain phyllosilicate (71–88 vol%), olivine (4–20 vol%), enstatite (2–6 vol%), magnetite (2–3 vol%), Fe‐sulfides (1–2 vol%), and calcite (~1 vol%). As aqueous alteration progressed, the abundance of Mg‐serpentine and magnetite in the CM chondrites increased. In contrast, calcite abundances in the CM1/2 and CM1 chondrites are often depleted relative to the CM2s. The modal data support the model, whereby metal and Fe‐rich matrix were the first components to be altered on the CM parent body(ies), before further hydration attacked the coarser Mg‐rich silicates found in chondrules and fragments. Based on the absence of tochilinite, we suggest that CM1 chondrites experienced increased alteration due to elevated temperatures (>120 °C), although higher water/rock ratios may also have played a role. The modal data provide constraints for interpreting the composition of asteroids and the mineralogy of samples returned from these bodies. We predict that “CM1‐like” asteroids, as has been proposed for Bennu—target for the OSIRIS‐REx mission—will have a high abundance of Mg‐rich phyllosilicates and Fe‐oxides, but be depleted in calcite.     

Phyllosilicates in the matrix of the unique carbonaceous chondrite Lewis Cliff 85332 and possible implications for the aqueous alteration of CI chondrites

Abstract— The fine-grained matrix of the unique, unequilibrated carbonaceous chondrite Lewis Cliff (LEW) 85332 has been studied by scanning electron microscopy (SEM), electron probe microanalysis (EPMA) and transmission electron microscopy (TEM). Compositionally, LEW 85332 has a matrix that is more Fe-rich than typical CI chondrites but has elemental abundance ratios that appear to be closer to CI matrices than to CM or CR chondrites. The mineralogy of the matrix is dominated by phyllosilicate phases that are predominantly interlayered Fe-rich serpentine/saponite; anhydrous silicate phases such as olivine and pyroxene are rare. Minor magnetite, troilite and ferrihydrite also occur associated with the phyllosilicates. Despite the high degree of weathering in LEW 85332, the phyllosilicates appear to have an extraterrestrial origin, but the highly variable Mg/Fe ratios of saponite may be the result of partial terrestrial oxidation of Fe-rich saponite to a more Mg-rich saponite and ferrihydrite. Alternatively, some of the ferrihydrite may have formed as a result of terrestrial weathering of Fe-Ni metal. The compositional and mineralogical data suggest that the matrix of LEW 85332 may represent a very early stage in the type of aqueous alteration experienced by the CI chondrites, although it is improbable that LEW 85332 was a precursor to the CI chondrites because of its high abundance of chondrules. The absence of carbonates, the high-Fe content of the matrix and phyllosilicate phases and relatively low abundance of magnetite all indicate that the degree of oxidation and leaching of LEW 85332 matrix was significantly less than that experienced by the CI chondrites. The absence of clear evidence for alteration of chondrules suggests that either the formation of the hydrous phases in the matrix occurred prior to accretion or that alteration occurred on a parent body and involved limited amounts of fluid, such that the reactions took place preferentially and exclusively within the fine-grained (anhydrous?) matrix materials.     

A plausible link between the asteroid 21 Lutetia and CH carbonaceous chondrites

A crucial topic in planetology research is establishing links between primitive meteorites and their parent asteroids. In this study, we investigate the feasibility of a connection between asteroids similar to 21 Lutetia, encountered by the Rosetta mission in July 2010, and the CH3 carbonaceous chondrite Pecora Escarpment 91467 (PCA 91467). Several spectra of this meteorite were acquired in the ultraviolet to near‐infrared (0.3–2.2 μm) and in the midinfrared to thermal infrared (2.5–30.0 μm or 4000 to ~333 cm⁻¹), and they are compared here to spectra from the asteroid 21 Lutetia. There are several similarities in absorption bands and overall spectral behavior between this CH3 meteorite and 21 Lutetia. Considering also that the bulk density of Lutetia is similar to that of CH chondrites, we suggest that this asteroid could be similar, or related to, the parent body of these meteorites, if not the parent body itself. However, the apparent surface diversity of Lutetia pointed out in previous studies indicates that it could simultaneously be related to other types of chondrites. Future discovery of additional unweathered CH chondrites could provide deeper insight in the possible connection between this family of metal‐rich carbonaceous chondrites and 21 Lutetia or other featureless, possibly hydrated high‐albedo asteroids.     

An investigation of the presence and nature of phyllosilicates on the surfaces of C asteroids by an analysis of the continuum slopes in their near‐infrared spectra

Abstract– To understand the nature of C asteroid surfaces, which are often related to phyllosilicates and C chondrites, we report near‐infrared spectra for a suite of phyllosilicates, heated to 100–1100 °C in 100 °C intervals, and compare the results for telescope IRTF spectra for 11 C asteroids. As C asteroids have relatively featureless spectra, we focus on “continuum plots” (1.0–1.75 μm slope against 1.8–2.5 μm slope). We compare the continuum plots of the 11 C asteroids and our heated phyllosilicates with literature data for C chondrites. The CI, CR, CK, and CV chondrite meteorites plot in the C asteroid field, whereas CM chondrites plot in a close but discrete field. All are well separated from the large phyllosilicate field. Heating kaolinite and montmorillonite to ≥700 °C moves their continua slopes into the C asteroid field, whereas chlorite and serpentine slopes move into the CM chondrite field. Water losses during heating are generally 10–15 wt% and were associated with a 20–70% albedo drop. Our data are consistent with surfaces of the C asteroids consisting of the dehydration products of montmorillonite whereas the CM chondrites are the dehydration products of serpentine and chlorite. The presence of opaque minerals and evaporites does not provide quantitative explanations for the difference in continua slopes of the phyllosilicates and C asteroids. The CM chondrites can also be linked to the C asteroids by heating. We suggest that the CM chondrites are interior samples, and the presence of a 3 μm feature in C asteroid spectra also indicates the excavation of material.     

IRTF observations of S complex and other asteroids: Implications for surface compositions,the presence of clinopyroxenes,and their relationship to meteorites

Abstract– We have obtained near‐infrared spectra for near‐Earth asteroids (NEA) and Main Belt asteroids by using NASA’s Infrared Telescope Facility. Most of the S complex classes of the Tholen‐Bus‐DeMeo scheme and the S(I)–S(VII) classes are represented. To help interpret the results, we examined visible/near‐IR spectra for ordinary chondrites. The unequilibrated ordinary chondrites (UOC) spectra contain a 2.3 μm feature which is absent in the spectra of the equilibrated ordinary chondrites (EOC). On the basis of literature data and new spectra low‐Ca clinopyroxenes, we suggest that the 2.3 μm in UOC is due to the presence of low‐Ca clinopyroxene in the UOC which is absent in EOC. While this difference can be seen in the raw spectra, we confirmed this observation using a modified Gaussian model (MGM) for spectral analysis. Both the UOC and the EOC plot in the S(IV) field of the band area ratio plot for asteroids. We suggest that many or most S(IV) asteroids have material resembling UOC on their surfaces. An internally heated ordinary chondrite parent object would have EOC material at depth and UOC material on the surface. Cosmic ray exposure ages, and K‐Ar ages for L chondrites, indicate that most EOC came from relatively few objects; however, the age distributions for UOC are unlike those of EOC. We suggest that while EOC come from the interiors of a limited number of S(IV) asteroids, the UOC come from the surfaces of a large number of S(IV) asteroids.     

Spectral reflectance properties of carbonaceous chondrites: 2. CM chondrites

We have examined the spectral reflectance properties and available modal mineralogies of 39 CM carbonaceous chondrites to determine their range of spectral variability and to diagnose their spectral features. We have also reviewed the published literature on CM mineralogy and subclassification, surveyed the published spectral literature and added new measurements of CM chondrites and relevant end members and mineral mixtures, and measured 11 parameters and searched pair-wise for correlations between all quantities. CM spectra are characterized by overall slopes that can range from modestly blue-sloped to red-sloped, with brighter spectra being generally more red-sloped. Spectral slopes, as measured by the 2.4:0.56 μm and 2.4 μm:visible region peak reflectance ratios, range from 0.90 to 2.32, and 0.81 to 2.24, respectively, with values <1 indicating blue-sloped spectra. Matrix-enriched CM spectra can be even more blue-sloped than bulk samples, with ratios as low as 0.85. There is no apparent correlation between spectral slope and grain size for CM chondrite spectra - both fine-grained powders and chips can exhibit blue-sloped spectra. Maximum reflectance across the 0.3-2.5 μm interval ranges from 2.9% to 20.0%, and from 2.8% to 14.0% at 0.56 μm. Matrix-enriched CM spectra can be darker than bulk samples, with maximum reflectance as low as 2.1%. CM spectra exhibit nearly ubiquitous absorption bands near 0.7, 0.9, and 1.1 μm, with depths up to 12%, and, less commonly, absorption bands in other wavelength regions (e.g., 0.4-0.5, 0.65, 2.2 μm). The depths of the 0.7, 0.9, and 1.1 μm absorption features vary largely in tandem, suggesting a single cause, specifically serpentine-group phyllosilicates. The generally high Fe content, high phyllosilicate abundance relative to mafic silicates, and dual Fe valence state in CM phyllosilicates, all suggest that the phyllosilicates will exhibit strong absorption bands in the 0.7 μm region (due to Fe³⁺-Fe²⁺ charge transfers), and the 0.9-1.2 μm region (due to Fe²⁺ crystal field transitions), and generally dominate over mafic silicates. CM petrologic subtypes exhibit a positive correlation between degree of aqueous alteration and depth of the 0.7 μm absorption band. This is consistent with the decrease in fine-grained opaques that accompanies aqueous alteration. There is no consistent relationship between degree of aqueous alteration and evidence for a 0.65 μm region saponite-group phyllosilicate absorption band. Spectra of different subsamples of a single CM can show large variations in absolute reflectance and overall slope. This is probably due to petrologic variations that likely exist within a single CM chondrite, as duplicate spectra for a single subsample show much less spectral variability. When the full suite of available CM spectra is considered, few clear spectral-compositional trends emerge. This indicates that multiple compositional and physical factors affect absolute reflectance, absorption band depths, and absorption band wavelength positions. Asteroids with reflectance spectra that exhibit absorption features consistent with CM spectra (i.e., absorption bands near 0.7 and 0.9 μm) include members from multiple taxonomic groups. This suggests that on CM parent bodies, aqueous alteration resulted in the consistent production of serpentine-group phyllosilicates, however resulting absolute reflectances and spectral shapes seen in CM reflectance spectra are highly variable, accounting for the presence of phyllosilicate features in reflectance spectra of asteroids across diverse taxonomic groups.     

A morphologic and crystallographic comparison of CV chondrite matrices

Meteoritic matrices are commonly classified by their modal mineralogy, alteration, and shock levels. Other “textural” characteristics are not generally considered in classification schemes, yet could carry important information about their genesis and evolution. Terrestrial rocks are routinely described by grain morphology, which has led to morphology‐driven classifications, and identification of controlling processes. This paper investigates three CV chondrites—Allende (CV3.2_oxA), Kaba (CV3.0_oxB), and Vigarano (CV3.3_red)—to determine the morphologic signature of olivine matrix grains. 2D grain size and shape, and crystallographic preferred orientations (CPOs) are quantified via electron backscatter diffraction mapping. Allende contains the largest and most elongate olivine grains, while Vigarano contains the least elongate, and Kaba contains the smallest grains. Weak but notable CPOs exist in some regions proximal to chondrules and one region distal to chondrules, and CPO geometries reveal a weak flattening of the matrix grains against the edge of chondrules within Allende. Kaba contains the least plastically deformed grains, and Allende contains the most plastically deformed grains. We tentatively infer that morphology is controlled by the characteristics of the available population of accreting grains, and aqueous and thermal alteration of the parent body. The extent of overall finite deformation is likely dictated by the location of the sample with respect to compression, the localized environment of the matrix with respect to surrounding material, and the post deformation temperature to induce grain annealing. Our systematic, quantitative process for characterizing meteorite matrices has the potential to provide a framework for comparison within and across meteorite classes, to help resolve how parent body processing differed across and between chondritic asteroids.     

Amorphous silicates as a record of solar nebular and parent body processes—A transmission electron microscope study of fine‐grained rims and matrix in three Antarctic CR chondrites

Renazzo‐type (CR) carbonaceous chondrites belong to one of the most pristine meteorite groups containing various early solar system components such as matrix and fine‐grained rims (FGRs), whose formation mechanisms are still debated. Here, we have investigated FGRs of three Antarctic CR chondrites (GRA 95229, MIL 07525, and EET 92161) by electron microscopy techniques. We specifically focused on the abundances and chemical compositions of the amorphous silicates within the rims and matrix by analytical transmission electron microscopy. Comparison of the amorphous silicate composition to a matrix area of GRA 95229 clearly shows a compositional relationship between the matrix and the fine‐grained rim, such as similar Mg/Si and Fe/Si ratios. This relationship and the abundance of the amorphous silicates in the rims strengthen a solar nebular origin and rule out a primary formation mechanism by parent body processes such as chondrule erosion. Moreover, our chemical analyses of the amorphous silicates and their abundance indicate that the CR rims experienced progressive alteration stages. According to our analyses, the GRA 95229 sample is the least altered one based on its high modal abundance of amorphous silicates (31%) and close‐to‐chondritic Fe/Si ratios, followed by MIL 07525 and finally EET 92161 with lesser amounts of amorphous silicates (12% and 5%, respectively) and higher Fe/Si ratios. Abundances and chemical compositions of amorphous silicates within matrix and rims are therefore suitable recorders to track different alteration stages on a submicron scale within variably altered CR chondrites.     

Aqueous alteration in the matrix of the Vigarano (CV3) carbonaceous chondrite

Abstract The matrix of Vigarano, a meteorite which belongs to the reduced subgroup of the CV3 chondrites, contains small amounts (<10%) of ferrihydrite and smectite. These hydrous minerals occur together as fine fibrous intergrowths between anhydrous silicate and oxide grains. Coarser crystals of ferrihydrite fill fractures that cut matrix minerals, and smectite also lines narrow channels within olivine grains. These channels may have formed by preferential alteration of olivines along (100)-parallel defects. Formation of ferrihydrite and smectite in the matrix of Vigarano was the result of mild aqueous alteration in a low-temperature (<150 °C), oxidising parent body environment. Partial equilibration of matrix olivines indicates that alteration was followed by thermal metamorphism with a peak temperature of 400–500 °C. Mineralogically similar alteration products, which also were formed by parent body processes, have previously been described from the matrices of four CV meteorites: Bali, Grosnaja, Kaba and Mokoia, all of which belong to the oxidised subgroup. This discovery of the products of oxidative aqueous alteration in Vigarano has important consequences for understanding the chemical and thermal history of the CV class of meteorites.