The onset of metamorphism in ordinary and carbonaceous chondrites

Abstract— Ordinary and carbonaceous chondrites of the lowest petrologic types were surveyed by X‐ray mapping techniques. A variety of metamorphic effects were noted and subjected to detailed analysis using electron microprobe, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and cathodoluminescence (CL) methods. The distribution of Cr in FeO‐rich olivine systematically changes as metamorphism increases between type 3.0 and type 3.2. Igneous zoning patterns are replaced by complex ones and Cr‐rich coatings develop on all grains. Cr distributions in olivine are controlled by the exsolution of a Cr‐rich phase, probably chromite. Cr in olivine may have been partly present as tetrahedrally coordinated Cr³⁺. Separation of chromite is nearly complete by petrologic type 3.2. The abundance of chondrules showing an inhomogeneous distribution of alkalis in mesostasis also increases with petrologic type. TEM shows this to be the result of crystallization of albite. Residual glass compositions systematically change during metamorphism, becoming increasingly rich in K. Glass in type I chondrules also gains alkalis during metamorphism. Both types of chondrules were open to an exchange of alkalis with opaque matrix and other chondrules. The matrix in the least metamorphosed chondrites is rich in S and Na. The S is lost from the matrix at the earliest stages of metamorphism due to coalescence of minute grains. Progressive heating also results in the loss of sulfides from chondrule rims and increases sulfide abundances in coarse matrix assemblages as well as inside chondrules. Alkalis initially leave the matrix and enter chondrules during early metamorphism. Feldspar subsequently nucleates in the matrix and Na re‐enters from chondrules. These metamorphic trends can be used to refine classification schemes for chondrites. Cr distributions in olivine are a highly effective tool for assigning petrologic types to the most primitive meteorites and can be used to subdivide types 3.0 and 3.1 into types 3.00 through 3.15. On this basis, the most primitive ordinary chondrite known is Semarkona, although even this meteorite has experienced a small amount of metamorphism. Allan Hills (ALH) A77307 is the least metamorphosed CO chondrite and shares many properties with the ungrouped carbonaceous chondrite Acfer 094. Analytical problems are significant for glasses in type II chondrules, as Na is easily lost during microprobe analysis. As a result, existing schemes for chondrule classification that are based on the alkali content of glasses need to be revised.     

A study of presolar material in hydrated lithic clasts from metal-rich carbonaceous chondrites

We report on the investigation of presolar grain inventories of hydrated lithic clasts in three metal-rich carbonaceous chondrites from the CR clan, Acfer 182 (CH3), Isheyevo (CH3/CB_b3), and Lewis Cliff (LEW) 85332 (C3-un), as well as the carbon- and nitrogen-isotopic compositions of the fine-grained clast material. Eleven presolar silicate grains as well as nine presolar silicon carbide (SiC) grains were identified in the clasts. Presolar silicate abundances range from 4 to 22 parts per million (ppm), significantly lower than in pristine meteorites and interplanetary dust particles (IDP), and comparable to recent findings for CM2s and CR2 interchondrule matrix. SiC concentrations lie between 9 and 23 ppm, and are comparable to the values for CI, CM, and CR chondrites. The results of our investigation suggest similar alteration pathways for the clast material, the interchondrule matrix of the CR2 chondrites, and the fine-grained fraction of CM2 chondrites. Fine-grained matter of all three meteorites contains moderate to high ¹⁵N-enrichments (~50‰ ≤ δ¹⁵N ≤ ~1600‰) compared to the terrestrial value, indicating the presence of primitive organic material. We observed no correlation between ¹⁵N-enrichments and presolar dust concentrations in the clasts. This is in contrast to the findings from a suite of primitive IDPs, which display in several cases enhanced bulk ¹⁵N/¹⁴N ratios and high presolar grain abundances of several hundred or even thousand ppm. The bulk ¹⁵N/¹⁴N ratios of the clasts are comparable to the range for primitive IDPs, suggesting a nitrogen carrier less susceptible to destruction by aqueous alteration than silicate stardust.     

Mechanisms accounting for variations in the proportions of carbonaceous and ordinary chondrites in different mass ranges

The number ratio of carbonaceous to ordinary chondrites (the CC/OC ratio) varies with mass. It is very high (≳90) in small mass ranges (10⁻⁸ to 10⁻¹² kg) among interplanetary dust particles and micrometeorites; it is moderately high (~5 to 30) for 1 to 10 m size fireball meteoroids (with estimated masses between ~10³ and ~10⁶ kg). In the range of most normal-sized meteorite falls (0.01–20 kg), the ratio is low (0.04–0.05); the ratio increases at greater mass ranges: at ≥200 kg, the ratio is 0.09; at ≥500 kg, the ratio is 0.20. The CC/OC ratio also increases from 0.05 to 0.16 for small meteorite finds (10⁻³ to 10⁻⁴ kg). High CC/OC ratios at low and high mass ranges are due to the predominance of CC material in the outer solar system. Small particles from this region spiral into the inner solar system typically in ≤10⁶ years due to Poynting–Robertson drag. Meter-sized meteoroids in this region are affected by Yarkovsky forces, pushing them into resonances where they are efficiently transferred to the inner solar system. Normal-sized meteorites are derived from centimeter-to-decimeter-sized meteoroids that have sluggish drift rates (i.e., they are less affected by the seasonal Yarkovsky effect) compared to larger bodies. Consequently, the centimeter-to-decimeter-sized meteoroids spend more time in interplanetary space (where they are subject to collisions) than larger objects. The greater friability of carbonaceous chondrites relative to ordinary chondrites tends to winnow the carbonaceous chondrites out in this size/mass range during their long interplanetary sojourn, thereby decreasing the CC/OC ratio.     

Metallic copper in ordinary chondrites

Abstract— Metallic Cu of moderately high purity (～985 mg/g Cu, ～15 mg/g Ni) occurs in at least 66% of ordinary chondrites (OC) as heterogeneously distributed, small (typically ≤20 μm) rounded to irregular grains. The mean modal abundance of metallic Cu in H, L and LL chondrites is low: 1.0 to 1.4 × 10^?4 vol%, corresponding to only 4–5% of the total Cu in OC whole rocks. In more than 75% of the metallic-Cu-bearing OC, at least some metallic Cu occurs at metallic-Fe-Ni-troilite grain boundaries. In some cases it also occurs within troilite, within metallic Fe-Ni, or at the boundaries these phases form with silicates or chromite. Ordinary chondrites that contain a relatively large number of occurrences of metallic Cu/mm² have a tendency to have experienced moderately high degrees of shock. Shock processes can cause local melting and transportation of metallic Fe-Ni and troilite; because metallic Cu is mainly associated with these phases, it also gets redistributed during shock events. In the most common petrographic assemblage containing metallic Cu, the Cu is adjacent to small irregular troilite grains surrounded by taenite plus tetrataenite; this assemblage resembles fizzed troilite and may have formed by localized shock melting or remelting of a metal-troilite assemblage.     

Glass-rich chondrules in ordinary chondrites

Abstract There are two types of glass-rich chondrules in unequilibrated ordinary chondrites (OC): (1) porphyritic chondrules containing 55–85 vol% glass or microcrystalline mesostasis and (2) nonporphyritic chondrules, containing 90–99 vol% glass. These two types are similar in mineralogy and bulk composition to previously described Al-rich chondrules in OC. In addition to Si-, Al- and Na-rich glass or Ca-Al-rich microcrystalline mesostasis, glass-rich chondrules contain dendritic and skeletal crystals of olivine, Al₂O₃-rich low-Ca pyroxene and fassaite. Some chondrules contain relict grains of forsterite ± Mg-Al spinel. We suggest that glass-rich chondrules were formed early in nebular history by melting fine-grained precursor materials rich in refractory (Ca, Al, Ti) and moderately volatile (Na, K) components (possibly related to Ca-Al-rich inclusions) admixed with coarse relict forsterite and spinel grains derived from previously disrupted type-I chondrules.     

Carbon in the matrices of ordinary chondrites

Abstract— Carbon in the petrologic matrices of a number of ordinary chondrites of groups H, L, and LL, and of types 3 through 6 was studied with a nuclear microprobe and a Raman microprobe. The majority of the matrices had carbon contents in the narrow range between 0.03 and 0.2 wt%. The carbon content decreased only slightly with increasing petrologic type. Carbon-rich coats around troilite and/or metal phases occured in five meteorites. Poorly ordered carbon was found in the matrices. The carbon in the meteorites of higher petrologic types was slightly better ordered than in the meteorites of lower types. The narrow range of carbon contents and the similarity of the structural form of carbon in the matrices of the measured ordinary chondrites, which represent all groups and types, imply that their matrices may contain a common component, which might be of interstellar origin.     

A sample preparation guide for clay-rich carbonaceous chondrites

The matrix of the C2-ungrouped Tarda meteorite contains abundant smectite minerals that swell and crumble when exposed to polar liquids, causing the sample to rapidly slake. This phenomenon presents a serious challenge when polishing the meteorite, as common polishing liquids used on carbonaceous chondrites, such as water, ethanol, ethylene glycol, and isopropyl alcohol, are polar and will cause the sample to swell, making it unsuitable for some analyses. Hexane and mineral oil are nonpolar liquids that were found to not induce swelling on highly expansive montmorillonite-clay analog material and were effectively integrated into a polishing procedure for Tarda. Here, we detail a procedure for mounting, cutting, and polishing the Tarda meteorite to prepare a surface that is suitable for a variety of sensitive techniques, such as electron microprobe analysis. This work offers a practical methodology for the preparation of other clay-rich samples, which may include the recently returned Ryugu and Bennu materials.     

Microchondrules in three unequilibrated ordinary chondrites

We report on a suite of microchondrules from three unequilibrated ordinary chondrites (UOCs). Microchondrules, a subset of chondrules that are ubiquitous components of UOCs, commonly occur in fine‐grained chondrule rims, although may also occur within matrix. Microchondrules have a variety of textures: cryptocrystalline, microporphyritic, radial, glassy. In some cases, their textures, and in many cases, their compositions, are similar to their larger host chondrules. Bulk compositions for both chondrule populations frequently overlap. The primary material that composes many of the microchondrules has compositions that are pyroxene‐normative and is similar to low‐Ca‐pyroxene phenocrysts from host chondrules; primary material rarely resembles olivine or plagioclase. Some microchondrules are composed of FeO‐rich material that has compositions similar to the bulk submicron fine‐grained rim material. These microchondrules, however, are not a common compositional type and probably represent secondary FeO‐enrichment. Microchondrules may also be porous, suggestive of degasing to form vesicles. Our work shows that the occurrence of microchondrules in chondrule rims is an important constraint that needs to be considered when evaluating chondrule‐forming mechanisms. We propose that microchondrules represent melted portions of the chondrule surfaces and/or the melt products of coagulated dust in the immediate vicinity of the larger chondrules. We suggest that, through recycling events, the outer surfaces of chondrules were heated enough to allow microchondrules to bud off as protuberances and become entrained in the surrounding dusty environment as chondrules were accreting fine‐grained rims. Microchondrules are thus byproducts of cyclic processing of chondrules in localized environments. Their occurrence in fine‐grained rims represents a snapshot of the chondrule‐forming environment. We evaluate mechanisms for microchondrule formation and hypothesize a potential link between the emergence of type II chondrules in the early solar system and the microchondrule‐bearing fine‐grained rims surrounding type I chondrules.     

Porosity and density of ordinary chondrites: Clues to the formation of friable and porous ordinary chondrites

Abstract— Densities and porosities of meteorites are physical properties that can be used to infer characteristics of asteroid interiors. We report density and porosity measurements of 42 pieces of 30 ordinary chondrites and provide a quantification of the errors of the gas pycnometer method used in this study. Based on our measurements, we find that no significant correlation exists between porosity and petrologic grade, chemical group, sample mass, bulk and grain density, or shock level. To investigate variations in porosity and density between pieces of a meteorite, we examined stones from two showers, Holbrook and Pultusk. Examination of nine samples of Holbrook suggests relative homogeneity in porosity and density between pieces of this shower. Measurements of three samples of Pultusk show homogeneity in bulk density, in contrast to Wilkison and Robinson (2000), a study that reported significant variations in bulk density between 11 samples of Pultusk. Finally, examination of two friable ordinary chondrites, Bjurböle and Allegan, reveal variability in friability and porosity among pieces of the same fall. We suggest that friable ordinary chondrites may have formed in a regolith or fault zone of an asteroid.     

A survey of clasts and large chondrules in ordinary chondrites

Abstract— We report the results of a survey of clasts and large (>5 mm) chondrules (macrochondrules) within the 833 ordinary chondrites of the Natural History Museum collection. Thirty-six macrochondrules and 24 clasts were identified and studied. Macrochondrules have textures and mineral assemblages like normal chondrules and so share a common origin. Clasts show evidence for fracturing from larger bodies and can be classified as either: (1) chemically fractionated if they have major and trace-element compositions differing substantially from most chondrules and clasts; (2) impact melt clasts if they have microporphyritic textures and signs that indicate they are derived from shock-melted chondritic material; (3) microporhyritic clasts if they are similar to the last category but lack evidence for derivation through shock melting; or (4) indeterminate clasts forming a diverse class that includes all those clasts that do not fit into the other categories.     

Nitrogen components in primitive ordinary chondrites

Abstract— Nitrogen and Ar in more than 20 primitive ordinary chondrites were studied by a stepped combustion method. Several N carriers that are characterized by N isotopic composition, N release pattern and trapped Ar release pattern are recognized in the primitive ordinary chondrites. Large fractions of anomalous N and associated Ar are removed by acid treatment in most cases. The N isotopic anomalies cannot be explained by known presolar grains (with a possible exception of graphite), and some of the N isotopic anomalies may be due to unknown presolar grains. There is no specific relationship between the type of N carriers contained in an ordinary chondrite and the chemical type (H, L, or LL) of the chondrite. It is likely that as a result of impacts, the carriers of isotopically anomalous N were mixed in various parent bodies as rock fragments rather than as individual fine particles. The presence of distinctive N isotopic anomalies in primitive meteorites indicates that the primitive solar nebula may have been heterogeneous either spatially or temporally.     

Terrestrial microfossils in Antarctic ordinary chondrites

Abstract— Microfossils have been separated and identified in four high metamorphic grade chondrites from Allan Hills and Queen Alexandra Range, Antarctica. Diatoms and opal phytoliths representing both marine and terrestrial flora were recognized among the dust removed from cracks in all meteorites studied. It is likely that contamination of Antarctic meteorites with such biogenic material is ubiquitous. Standard clean room procedures to avoid laboratory introduction of microfossils into the meteorites were followed, and the genera and species identified so far are characteristic of marine, freshwater, and continental environments. The most probable mechanism for introduction of the microfossils into the meteorites is eolian transport to and on the polar ice cap. It is likely that wind-driven systems may sample atmospherically transported material from large portions of the southern hemisphere. Entrainment of terrestrial microfossils is probably a typical interaction of meteorites with the Antarctic environment and must be recognized and accounted for in any attempt to use Antarctic meteorites as sources of extraterrestrial life forms. Organic molecules derived from microfossils are likely to be pervasive throughout any crack network present in a meteorite at all scales from millimeter to submicron. Cracks are a ubiquitous consequence of weathering in and on the Antarctic ice and the probability that crack surfaces contain terrestrial organic materials is high.     

Spectral reflectance properties of carbonaceous chondrites: 3. CR chondrites

Powdered samples of a suite of 14 CR and CR-like chondrites, ranging from petrologic grade 1 to 3, were spectrally characterized over the 0.3–2.5 μm interval as part of a larger study of carbonaceous chondrite reflectance spectra. Spectral analysis was complicated by absorption bands due to Fe oxyhydroxides near 0.9 μm, resulting from terrestrial weathering. This absorption feature masks expected absorption bands due to constituent silicates in this region. In spite of this interference, most of the CR spectra exhibit absorption bands attributable to silicates, in particular an absorption feature due to Fe²⁺-bearing phyllosilicates near 1.1 μm. Mafic silicate absorption bands are weak to nonexistent due to a number of factors, including low Fe content, low degree of silicate crystallinity in some cases, and presence of fine-grained, finely dispersed opaques. With increasing aqueous alteration, phyllosilicate: mafic silicate ratios increase, resulting in more resolvable phyllosilicate absorption bands in the 1.1 μm region. In the most phyllosilicate-rich CR chondrite, GRO 95577 (CR1), an additional possible phyllosilicate absorption band is seen at 2.38 μm. In contrast to CM spectra, CR spectra generally do not exhibit an absorption band in the 0.65–0.7 μm region, which is attributable to Fe³⁺–Fe²⁺ charge transfers, suggesting that CR phyllosilicates are not as Fe³⁺-rich as CM phyllosilicates. CR2 and CR3 spectra are uniformly red-sloped, likely due to the presence of abundant Fe–Ni metal. Absolute reflectance seems to decrease with increasing degree of aqueous alteration, perhaps due to the formation of fine-grained opaques from pre-existing metal. Overall, CR spectra are characterized by widely varying reflectance (4–21% maximum reflectance), weak silicate absorption bands in the 0.9–1.3 μm region, overall red slopes, and the lack of an Fe³⁺–Fe²⁺ charge transfer absorption band in the 0.65–0.7 μm region.     

Spectral reflectance properties of carbonaceous chondrites: 6. CV chondrites

Multiple reflectance spectra of 11 CV chondrites have been measured to determine spectral–compositional relationships for this meteorite class and to aid the search for CV parent bodies. The reflectance of CV chondrite spectra is variable, ranging from ～5% to 13% at 0.56 μm, and ～5% to 15% at the 0.7 μm region local reflectance maximum. Overall slopes range from slightly blue to red for powders, while slab spectra are strongly blue-sloped. With increasing average grain size and/or removal of the finest fraction, CV spectra generally become more blue-sloped. CV spectra are characterized by ubiquitous absorption features in the 1 and 2 μm regions. The 1 μm region is usually characterized by a band centered near 1.05–1.08 μm and a band or shoulder near 1.3 μm that are characteristic of Fe-rich olivine. Band depths in the 1 μm region for powdered CVs and slabs range from ～1% to 10%. The 2 μm region is characterized by a region of broad absorption that extends beyond 2 μm and usually includes band minima near 1.95 and 2.1 μm; these features are characteristic of Fe²⁺-bearing spinel. The sample suite is not comprehensive enough to firmly establish whether spectral differences exist between CV_R, CV_OxA, and CV_OxB subclasses, or as a function of metamorphic grade. However, we believe that the mineralogic and petrologic differences that exist between these classes, and with varying petrologic subtype (CV3.0–>3.7), may not be significant enough to result in measurable spectral differences that exceed spectral variations within a subgroup, within an individual meteorite, or as a function of grain size. Terrestrial weathering seems to affect CV spectra most noticeably in the visible region, resulting in more red-sloped spectra for finds as compared to falls. The search for CV parent bodies should focus on the detection of olivine and spinel absorption bands, specifically absorption features near 1.05, 1.3, 1.95, and 2.1 μm, as these are the most commonly seen spectral features of CV chondrites.     

Spectral reflectance properties of carbonaceous chondrites: 1. CI chondrites

Existing reflectance spectra of CI chondrites (18 spectra of 3 CIs) have been augmented with new (18 spectra of 2 CIs) reflectance spectra to ascertain the spectral variability of this meteorite class and provide insights into their spectral properties as a function of grain size, composition, particle packing, and viewing geometry. Particle packing and viewing geometry effects have not previously been examined for CI chondrites. The current analysis is focused on the 0.3-2.5 μm interval, as this region is available for the largest number of CI spectra. Reflectance spectra of powdered CI1 chondrites are uniformly dark (<10% maximum reflectance) but otherwise exhibit a high degree of spectral variability. Overall spectral slopes range from red (increasing reflectance with increasing wavelength) to blue (decreasing reflectance with increasing wavelength). A number of the CI spectra exhibit weak (<5% deep) absorption bands that can be attributed to both phyllosilicates and magnetite. Very weak absorption bands attributable to other CI phases, such as carbonates, sulfates, and organic matter may be present in one or a few spectra, but their identification is not robust. We found that darker spectra are generally correlated with bluer spectral slopes: a behavior most consistent with an increasing abundance of fine-grained magnetite and/or insoluble organic material (IOM), as no other CI opaque phase appears able to produce concurrent darkening and bluing. Magnetite can also explain the presence of an absorption feature near 1 μm in some CI spectra. The most blue-sloped spectra are generally associated with the larger grain size samples. For incidence and emission angles <60°, increasing phase angle results in darker and redder spectra, particularly below ∼1 μm. At high incidence angles (60°), increasing emission angle results in brighter and redder spectra. More densely packed samples and underdense (fluffed) samples show lower overall reflectance than normally packed and flat-surface powdered samples. Some B-class asteroids exhibit selected spectral properties consistent with CI chondrites, although perfect spectral matches have not been found. Because many CI chondrite spectra exhibit absorption features that can be related to specific mineral phases, the search for CI parent bodies can fruitfully be conducted using such parameters.     

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.     

Formation of the parent bodies of the carbonaceous chondrites

We have carried out extensive particle track studies for several C2 chondrites. On the basis of these and the available data on spallogenic stable and radioactive nuclides in several C1 and C2 chondrites, we have constructed a scenario for the precompaction irradiation of these meteorites. We discuss the rather severe constraints which these data place on the events leading to the formation of the parent bodies of the carbonaceous chondrites. Our analyses suggest that the precompaction solar flare and solar wind irradiation of the individual components most probably occurred primarily while the matter had accreted to form swarms of centimeter- to meter-sized bodies. This irradiation occured very early, within a few hundred my of the birth of the solar system; the pressure in the solar system had then dropped below 10^?9 atm. Further, the model assumes that soon after the irradiation of carbonaceous matter as swarms, the small bodies coalesced to form kilometer-sized objects, in time scales of 10^5±1 years, a constraint defined by the low cosmogenic exposure ages of these meteorites. Collisions among these objects led to the formation of much-larger-sized parent bodies of the carbonaceous chondrites. Implicit in this model is the existence of “irradiated” components at all depths in the parent bodies, which formed out of the irradiated swarm material.     

The insoluble carbonaceous material of CM chondrites: A possible source of discrete organic compounds under hydrothermal conditions

Abstract— We report on the molecular analyses of the water‐ and solvent‐soluble organic compounds released from the insoluble organic material (IOM) of the Murray meteorite upon treatment with weight‐equivalent amounts of water and under conditions of elevated temperature and pressure. A varied suite of compounds was identified by gas chromatography‐mass spectrometry (GC‐MS). C₃‐C₁₇ alkyl dicarboxylic acids and N‐ and O‐containing hydroaromatic and aromatic compounds were found in the water extracts. The solvent extracts contained N‐, O‐, and S‐containing aromatic compounds, a large number of their isomers and homologs, and a series of polycyclic aromatic hydrocarbons (PAHs) of up to five rings, together with noncondensed aromatic species such as substituted benzenes, biphenyl, and terphenyls as well as their substituted homologs, and hydrated PAHs. Isotopic analyses showed that residue IOMs after hydrothermal treatment had lower deuterium and ¹⁵N content than the untreated material (ΔD = ?833‰ and Δ¹⁵N = ?24.1) but did not differ from it in ¹³C composition. The effect of the hydrothermolytic release was recorded in significant differences between the NMR spectra of untreated and residue IOM. A possible relation to common precursors for the dicarboxylic acids found in the IOM and bulk extracts is discussed.     

Origin of hibonite-pyroxene spherules found in carbonaceous chondrites

Abstract— We have studied both of the known glass-free, hibonite-pyroxene spherules: MYSM3, from Murray (CM2), and Y17–6, from Yamato 791717 (CO3). They consist of hibonite plates (～2 wt% TiO^tot₂) enclosed in Al-rich pyroxene that has such high amounts of CaTs (CaAl₂SiO₆) component, up to ～80 mol%, that it must have crystallized metastably. Within the pyroxene, abundances of MgO and SiO₂ are strongly correlated with each other and are anticorrelated with those of Al₂O₃, reflecting an anticorrelation between the diopside and CaTs components of the pyroxene. In contrast with previous results for Type B fassaite, however, we do not observe an anticorrelation between MgO and TiO^tot₂, possibly reflecting different relative distribution coefficients for Ti³⁺ and Ti⁴⁺ in the aluminous pyroxene of the spherules from those found for fassaite in Type B inclusions. Previously described hibonite-silicate spherules have ²⁶Mg deficits but the present samples do not. Furthermore, the pyroxene in Y17-6 has excess ²⁶Mg, while the hibonite it encloses does not, indicating that the two phases either had different initial ²⁶Al/²⁷Al ratios or different initial ²⁶Mg/²⁴Mg ratios. The Ti isotopic compositions of the present samples are highly unusual: δ⁵⁰Ti = 103.4 ± 5.2%o in MYSM3 and -61.4 ± 4.1%0 in Y17-6, which are among the largest ⁵⁰Ti anomalies reported for any refractory inclusion. The textures suggest that hibonite crystallized first; but based on the calculated bulk compositions of both spherules, it is not the liquidus phase in either sample, which suggests that the hibonite in both samples is relict. The presence of ragged hibonite grains in MYSM3 and rounded hibonite grains in Y17-6 and a lack of isotopic equilibrium between pyroxene and hibonite support this conclusion. The spherules crystallized from liquid droplets that probably formed as a result of the melting of solid precursor grains that included hibonite. The heating events were too short and/or not hot enough to melt all the hibonite. The droplets cooled quickly enough that CaTs-rich pyroxene crystallized instead of anorthite. Based on the observed differences in isotopic composition, it is unlikely that the precursors of the present samples formed in the same reservoir as each other or as the previously described hibonite-silicate spherules, providing further evidence of the isotopic heterogeneity of the early solar nebula.