Modeling aqueous alteration of CM carbonaceous chondrites

Abstract— Results from an inorganic geochemical modeling study support a scenario in which low‐temperature aqueous alteration of an anhydrous CM asteroidal parent body and melt water from H₂O and CO₂ ices produces the altered assemblage observed in CM carbonaceous chondrites (chrysotile, greenalite, tochilinite, cronstedtite and minor calcite and magnetite). We consider a range of possible precursor mineral assemblages, varying with respect to the Fe‐oxidation state of the initial anhydrous phases. The aqueous solutions produced by this alteration are generally strongly basic and reducing and a large quantity of H₂, and possible CH₄, gas can be released during aqueous alteration.     

Hydrothermal alteration experiments of enstatite: Implications for aqueous alteration of carbonaceous chondrites

Abstract— Enstatite is one of the major constituent minerals in carbonaceous chondrites. Hydrothermal alteration experiments (26 in total) of enstatite were carried out at pH 0, 6, 7, 12, 13, and 14, at temperatures of 100, 200, and 300 °C, and for run durations of 24, 72, 168, and 336 h in order to provide constraints on the aqueous‐alteration conditions of the meteorites. The recovered samples were studied in detail by using powder X‐ray diffraction, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Under acidic and mildly acidic conditions (pH 0, 6), no significant alteration occurred, whereas under neutral to alkaline conditions (pH 7–14), serpentine and saponite formed in various proportions by replacing enstatite. At 300 °C for 168 h, serpentine formed under neutral to moderately alkaline conditions (pH 7, 12), and serpentine and saponite formed as unit cell‐scale coherent intergrowths under highly alkaline conditions (pH 13, 14). The amounts of phyllosilicates have a tendency to increase with increasing pH, temperature, and run duration. There is also a tendency for saponite to form at higher pH and temperature and under longer run‐durations than serpentine. The results indicate that alteration of enstatite is strongly dependent on the experimental conditions, especially pH. They suggest that CM chondrites experienced aqueous alteration under neutral to alkaline conditions, whereas CV and CI chondrites experienced aqueous alteration under more alkaline conditions. The results also suggest that aqueous alteration in CI chondrites occurred at higher temperatures than in CM chondrites, and aqueous alteration in CV chondrites occurred at even higher temperatures than in CI chondrites.     

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.     

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.     

The structure and composition of metal particles in two type 6 ordinary chondrites

Abstract— The purpose of this study is to examine, using light optical and electron optical techniques, the microstructure and composition of metal particles in ordinary chondritic meteorites. This examination will lead to the understanding of the low temperature thermal history of metal particles in their host chondrites. Two type 6 falls were chosen for study: Kernouvé (H6) and Saint Severin (LL6). In both meteorites, the taenite particles consisted of a narrow rim of high Ni taenite and a central region of cloudy zone similar to the phases observed in iron meteorites. The cloudy zone microstructure was coarser in Saint Severin than in Kernouvé due to the higher bulk Ni content of the taenite and the slower cooling rate, 3 K Ma^?1 vs. 17 K Ma^?1. Three microstructural zones were observed within the high Ni taenite region in both meteorites. The origin of the multiple zones is unknown but is most likely due to the high Ni taenite cooling into the two phase γ″ (FeNi) + γ′ (FeNi₃) region of the low temperature Fe-Ni phase diagram. Another explanation may be the presence of uniform size antiphase boundaries within the high Ni taenite. Finally, abnormally wide high Ni taenite regions are observed bordering troilite. The wide zones are probably caused by the diffusion of Ni from troilite into the high Ni taenite borders at low cooling temperatures.     

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.     

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.     

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.     

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.     

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.     

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.     

Aqueous alteration of kamacite in CM chondrites

Abstract– The study of aqueous alteration of kamacite in CM chondrites provides insight on the conditions, products, and relative timing of aqueous alteration. We studied unaltered, partially altered, and fully altered kamacite grains from Murray, Murchison, Cold Bokkeveld, and Nogoya using optical microscopy, electron microprobe analysis, scanning electron microscopy, and Raman spectroscopy. From textual evidence and chemical analysis, we established three separate microchemical environments. 1) In a microchemical environment with a high S activity, kamacite alters to form tochilinite, P‐bearing sulfides, eskolaite, and schreibersite. Mass balance calculations show that 81% of the Fe in kamacite is removed from the alteration region, making it available for the formation of other minerals or Fe‐rich aureoles. The release of Fe can alter the mesostasis of type‐I chondrules forming cronstedtite. 2) In a microchemical environment with a high Si activity and a low S activity, kamacite alters to form cronstedtite with small accessory sulfide inclusions. 3) A microchemical environment with limited S and Si activity results in kamacite alteration forming magnetite. The resulting magnetite retains associated Ni that can distinguish it from precipitated magnetite. In addition, the accessory phases of pentlandite and apatite can be formed if S or Ca are present. Finally, we note that small tochilinite grains in the matrix lack typical Ni, P, and Co levels, suggesting that they did not form from kamacite but possibly by sulfidization of magnetite.     

Bleached chondrules: Evidence for widespread aqueous processes on the parent asteroids of ordinary chondrites

Abstract— We present the first detailed study of a population of texturally distinct chondrules previously described by Kurat (1969), Christophe Michel‐Lévy (1976), and Skinner et al. (1989) that are sharply depleted in alkalis and Al in their outer portions. These “bleached” chondrules, which are exclusively radial pyroxene and cryptocrystalline in texture, have porous outer zones where mesostasis has been lost. Bleached chondrules are present in all type 3 ordinary chondrites and are present in lower abundances in types 4–6. They are most abundant in the L and LL groups, apparently less common in H chondrites, and absent in enstatite chondrites. We used x‐ray mapping and traditional electron microprobe techniques to characterize bleached chondrules in a cross section of ordinary chondrites. We studied bleached chondrules from Semarkona by ion microprobe for trace elements and H isotopes, and by transmission electron microscopy. Chondrule bleaching was the result of low‐temperature alteration by aqueous fluids flowing through finegrained chondrite matrix prior to thermal metamorphism. During aqueous alteration, interstitial glass dissolved and was partially replaced by phyllosilicates, troilite was altered to pentlandite, but pyroxene was completely unaffected. Calcium‐rich zones formed at the inner margins of the bleached zones, either as the result of the early stages of metamorphism or because of fluid‐chondrule reaction. The mineralogy of bleached chondrules is extremely sensitive to thermal metamorphism in type 3 ordinary chondrites, and bleached zones provide a favorable location for the growth of metamorphic minerals in higher petrologic types. The ubiquitous presence of bleached chondrules in ordinary chondrites implies that they all experienced aqueous alteration early in their asteroidal histories, but there is no relationship between the degree of alteration and metamorphic grade. A correlation between the oxidation state of chondrite groups and their degree of aqueous alteration is consistent with the source of water being either accreted ices or water released during oxidation of organic matter. Ordinary chondrites were probably open systems after accretion, and aqueous fluids may have carried volatile elements with them during dehydration. Individual radial pyroxene and cryptocrystalline chondrules were certainly open systems in all chondrites that experienced aqueous alteration leading to bleaching.     

Peak metamorphic temperatures in type 6 ordinary chondrites: An evaluation of pyroxene and plagioclase geothermometry

Abstract— Quantifying the peak temperatures achieved during metamorphism is critical for understanding the thermal histories of ordinary chondrite parent bodies. Various geothermometers have been used to estimate equilibration temperatures for chondrites of the highest metamorphic grade (type 6), but results are inconsistent and span hundreds of degrees. Because different geothermometers and calibration models were used with different meteorites, it is unclear whether variations in peak temperatures represent actual ranges of metamorphic conditions within type 6 chondrites or differences in model calibrations. We addressed this problem by performing twopyroxene geothermometry, using QUILF95, on the same type 6 chondrites for which peak temperatures were estimated using the plagioclase geothermometer (Nakamuta and Motomura 1999). We also calculated temperatures for published pyroxene analyses from other type 6 H, L, and LL chondrites to determine the most representative peak metamorphic temperatures for ordinary chondrites. Pyroxenes record a narrow, overlapping range of temperatures in H6 (865–926 °C), L6 (812–934 °C), and LL6 (874–945 °C) chondrites. Plagioclase temperature estimates are 96–179 °C lower than pyroxenes in the same type 6 meteorites. Plagioclase estimates may not reflect peak metamorphic temperatures because chondrule glass probably recrystallized to plagioclase prior to reaching the metamorphic peak. The average temperature for H, L, and LL chondrites (～900 °C), which agrees with previously published oxygen isotope geothermometry, is at least 50 °C lower than the peak temperatures used in current asteroid thermal evolution models. This difference may require minor adjustments to thermal model calculations.     

Molecular and isotopic indicators of alteration in CR chondrites

Abstract— The CR group of carbonaceous chondrites may represent some of the most primitive extraterrestrial materials available for analysis. However, in contrast to other chondrite groups, the CR organic fraction is poorly characterized. The carbonaceous chondrite literature shows that relatively anhydrous thermal processing results in a condensed, poorly alkylated, O‐poor macromolecular material, while for aqueous processing the converse is true. Such characteristics can be used to discern the alteration histories of the carbonaceous chondrites. We have performed bulk elemental and isotopic analysis and flash pyrolysis on four CR chondrites (Renazzo, Al Rais, Elephant Moraine [EET] 87770, and Yamato [Y‐] 790112) to determine the nature of their organic component. Renazzo, Al Rais, and Y‐790112 release qualitatively similar pyrolysis products, although there are some variations. Al Rais' macromolecular structure contains substantially higher relative abundances of alkylated and oxidized species and relatively lighter δ¹⁵N, suggesting that it has endured more extensive aqueous processing than the other CR chondrites. Renazzo appears relatively unprocessed, with a low degree of alkylation, a lack of detectable nitrogen‐bearing components, and low methylnaphthalene ratio. EET 87770's low abundance of alkylated species suggests its macromolecular structure may be relatively condensed, with condensation potentially assisted by a period of mild thermal alteration.     

Thermoluminescence sensitivity and thermal history of type 3 ordinary chondrites: Eleven new type 3.0–3.1 chondrites and possible explanations for differences among H,L, and LL chondrites

Abstract— We review induced thermoluminescence (TL) data for 102 unequilibrated ordinary chondrites (UOCs), many data just published in abstracts, in order to identify particularly primitive UOCs and further explore TL systematics that may have implications for the history of the chondrites and their parent body. We have identified 11 UOCs of petrologic types 3.0–3.1: Adrar 003, Elephant Moraine (EET) 90066, EET 90161, Grosvenor Mountains (GRO) 95502, Lewis Cliff (LEW) 88477, Meteorite Hills (MET) 96503, Yamato (Y)‐790787, Y‐791324, Y‐791558, Y‐793565, and Y‐793596. These samples represent an important new resource for researchers interested in the nature of primitive solar system materials. Previously reported trends in which TL sensitivity increases with TL peak temperature and TL peak width, which we interpret in terms of crystallization of feldspar in the ordered or disordered forms during metamorphism, are confirmed by the new data. Importantly, the present data strengthen the trend described earlier in which the mean level of metamorphism experienced by UOCs increases along the series LL, L and H. This suggests either different burial depths for the UOCs from each class, or formation at similar depths in regoliths of different thickness.     

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.     

Progressive alteration in CV3 chondrites: More evidence for asteroidal alteration

Abstract— The oxidized CV3 chondrites can be divided into two major subgroups or lithologies, Bali-like (CV3_oxB) and Allende-like (CV3_oxA), in which chondrules, calcium-aluminum-rich inclusions (CAIs) and matrices show characteristic alteration features (Weisberg et al, 1997; Krot et al, 1997d; Kimura and Ikeda, 1997). The CV3_oxB lithology is present in Bali, Kaba, parts of the Mokoia breccia and, possibly, in Grosnaja and Allan Hills (ALH) 85006. It is characterized by the presence of the secondary low-Ca phyllosilicates (saponite and sodium phlogopite), magnetite, Ni-rich sulfides, fayalite (Fa>₉₀), Ca-Fe-rich pyroxenes (Fs_10–50Wo_45–50) and andradite. Phyllosilicates replace primary Ca-rich minerals in chondrules and CAIs, which suggests mobilization of Ca during aqueous alteration. Magnetite nodules are replaced to various degrees by fayalite, Ca-Fe-rich pyroxenes and minor andradite. Fayalite veins crosscut fine-grained rims around chondrules and extend into the matrix. Thermodynamic analysis of the observed reactions indicates that they could have occurred at relatively low temperatures (<300 °C) in the presence of aqueous solutions. Oxygen isotopic compositions of the coexisting magnetite and fayalite plot close to the terrestrial fractionation line with large Δ¹⁸O_{fayalite-magnetite} fractionation (～20%). We infer that phyllosilicates, magnetite, fayalite, Ca-Fe-rich pyroxenes and andradite formed at relatively low temperatures (<300 °C) by fluid-rock interaction in an asteroidal environment. Secondary fayalite and phyllosilicates are virtually absent in chondrules and CAIs in the CV3_oxA lithology, which is present in Allende and its dark inclusions, Axtell, ALHA81258, ALH 84028, Lewis Cliff (LEW) 86006, and parts of the Mokoia and Vigarano breccias. Instead secondary nepheline, sodalite, and fayalitic olivine are common. Fayalitic olivine in chondrules replaces low-Ca pyroxenes and rims and veins forsterite grains; it also forms coarse lath-shaped grains in matrix. Secondary Ca-Fe-rich pyroxenes are abundant. We infer that the CV3_oxA lithology experienced alteration at higher temperatures than the CV3_oxB lithology. The presence of the reduced and CV3_oxA lithologies in the Vigarano breccia and CV3_oxA and CV3_oXB lithologies in the Mokoia breccia indicates that all CV3 chondrites came from one heterogeneously altered asteroid. The metamorphosed clasts in Mokoia (Krot and Hutcheon, 1997) may be rare samples of the hotter interior of the CV asteroid. We conclude that the alteration features observed in the oxidized CV3 chondrites resulted from the fluid-rock interaction in an asteroid during progressive metamorphism of a heterogeneous mixture of ices and anhydrous materials mineralogically similar to the reduced CV3 chondrites.     

Neon produced by solar cosmic rays in ordinary chondrites

Solar‐cosmic‐ray‐produced Ne (SCR‐Ne), in the form of low cosmogenic ²¹Ne/²²Ne ratios (²¹Ne/²²Ne_cos <0.8), is more likely to be found in rare meteorite classes, like Martian meteorites, than in ordinary chondrites. This may be the result of a sampling bias: SCR‐Ne is better preserved in meteorites with small preatmospheric radii and these specimens are often only studied if they belong to unusual or rare classes. We measured He and Ne isotopic concentrations and nuclear tracks in 25 small unpaired ordinary chondrites from Oman. Most chondrites have been intensively heated during atmospheric entry as evidenced by the disturbed track records, the low ³He/²¹Ne ratios, the low ⁴He concentrations, and the high peak release temperatures. Concentration depth profiles indicate significant degassing; however, the Ne isotopes are mainly undisturbed. Remarkably, six chondrites have low ²¹Ne/²²Ne_cos in the range 0.711–0.805. Using a new physical model for the calculation of SCR production rates, we show that four of the chondrites contain up to ~20% of SCR‐Ne; they are analyzed in terms of preatmospheric sizes, cosmic ray exposure ages, mass ablation losses, and orbits. We conclude that SCR‐Ne is preserved, regardless of the meteorite class, in specimens with small preatmospheric radii. Sampling bias explains the predominance of SCR‐Ne in rare meteorites, although we cannot exclude that SCR‐Ne is more common in Martian meteorites than it is in small ordinary chondrites.