Geochemistry of the ungrouped carbonaceous chondrite Tagish Lake,the anomalous CM chondrite Bells,and comparison with CI and CM chondrites

Abstract— I have determined the composition via instrumental neutron activation analysis of a bulk pristine sample of the Tagish Lake carbonaceous chondrite fall, along with bulk samples of the CI chondrite Orgueil and of several CM chondrites. Tagish Lake has a mean of refractory lithophile element/Cr ratios like those of CM chondrites, and distinctly higher than the CI chondrite mean. Tagish Lake exhibits abundances of the moderately volatile lithophile elements Na and K that are slightly higher than those of mean CM chondrites. Refractory through moderately volatile siderophile element abundances in Tagish Lake are like those of CM chondrites. Tagish Lake is distinct from CM chondrites in abundances of the most volatile elements. Mean CI‐normalized Se/Co, Zn/Co and Cs/Co for Tagish Lake are 0.68 ± 0.01, 0.71 ± 0.07 and 0.76 ± 0.02, while for all available CM chondrite determinations, these ratios lie between 0.31 and 0.61, between 0.32 and 0.58, and between 0.39 and 0.74, respectively. Considering petrography, and oxygen isotopic and elemental compositions, Tagish Lake is an ungrouped member of the carbonaceous chondrite clan. The overall abundance pattern is similar to those of CM chondrites, indicating that Tagish Lake and CMs experienced very similar nebular fractionations. Bells is a CM chondrite with unusual petrologic characteristics. Bells has a mean CI‐normalized refractory lithophile element/Cr ratio of 0.96, lower than for any other CM chondrite, but shows CI‐normalized moderately volatile lithophile element/Cr ratios within the ranges of other CM chondrites, except for Na which is low. Iridium, Co, Ni and Fe abundances are like those of CM chondrites, but the moderately volatile siderophile elements, Au, As and Sb, have abundances below the ranges for CM chondrites. Abundances of the moderately volatile elements Se and Zn of Bells are within the CM ranges. Bells is best classified as an anomalous CM chondrite.     

THE CHEMICAL COMPOSITION OF MAJOR ELEMENTS AND HEAVY TRACE METALS IN CHONDRITES PARAMBÙ AND MARILIA

The chemical composition of the newly observed fallen chondrites Parambù, 1967, and Marilia, 1971, was determined. Wet chemical methods were used for major elements analyses and the abundances of heavy trace elements from tungsten to uranium were determined by spark source mass spectrometry. The chemical composition confirmed the classification of Marilia as an H-group chondrite by Avanzo et al. (1973): Parambù was classified as an LL-group chondrite.     

Comparison of the Murchison CM2 and Allende CV3 chondrites

The size distribution, abundance, and physical and chemical characteristics of chondritic inclusions are key features that define the chondrite groups. We present statistics on the size and abundance of the macroscopic components (inclusions) in the Murchison (CM2) and Allende (CV3) chondrites and measure their general chemical trends using established X‐ray mapping techniques. This study provides a fine‐scale assessment of the two meteorites and a semiquantitative evaluation of the relative abundances of elements and their distribution among meteorite components. Murchison contains 72% matrix and 28% inclusions; Allende contains 57% and 43%, respectively. A broad range of inclusion sizes and relative abundances has been reported for these meteorites, which demonstrates the necessity for a more standardized approach to measuring these characteristics. Nonetheless, the characteristic mean sizes of inclusions in Allende are consistently larger than those in Murchison. We draw two significant conclusions (1) these two meteorites sampled distinct populations of chondrules and refractory inclusions, and (2) complementary Mg/Si ratios between chondrules and matrix are observed in both Murchison and Allende. Both support the idea that chondrules and matrix within each chondrite group originated in single reservoirs of precursors with approximately solar Mg/Si ratios, providing a constraint on astrophysical models of the origin of chondrite parent bodies.     

RARE EARTH AND OTHER ABUNDANCES IN THE MURCHISON CARBONACEOUS METEORITE

The abundances of 27 elements are reported for the Murchison meteorite. Nine of these elements (Al, Ca, Fe, Mn, Na, K, Cr, Co, and Sc) have been determined previously for different Murchison specimens. Abundances for 18 elements (In, Cd, V, Y, and REE) are new data for this meteorite. The chemical composition is similar to the type II carbonaceous chondrites, particularly on the basis of REE, Mn, and In abundances.     

THE CHEMICAL COMPOSITIONS OF THE STONE METEORITES YAMATO (a), (b), (c) and (d), AND NUMAKAÍ

The stone meteorites Yamato (a), (b), (c) and (d) were found in Antarctica in 1969, and the chondrite Numakai was seen to fall in Hokkaido, Japan, in 1925. The chemical compositions of these meteorites have been determined by classical and instrumental methods. With the help of the stepwise fractional dissolution method the chemical composition confirmed the author's previous classification of Yamato (a), (b), (c) and (d) as enstatite chondrite, Ca-poor achondrite, type III carbonaceous chondrite and H-group chondrite, respectively. Numakai is classified as an H-group olivine-bronzite chondrite. The distribution of the major elements in each phase of these chondrites is discussed.     

The GRO 95577 CR1 chondrite and hydration of the CR parent body

Abstract— We carried out a petrologic and instrumental neutron activation analysis (INAA) whole chondrite compositional study of Grosvenor Mountains (GRO) 95577. GRO 95577 has many petrological similarities to the CR chondrites. Although the INAA data show patterns indicative of terrestrial weathering, some of the elemental abundances are consistent with a relationship to CR chondrites. The oxygen isotopic composition of GRO 95577 plots close to the Renazzo CR chondrite on the three‐isotope diagram. However, GRO 95577 is remarkable in that the chondrules are completely hydrated, consisting almost entirely of phyllosilicates, magnetite, and sulfides. Although GRO 95577 is completely hydrated, the initial chondrule textures are perfectly preserved. The chondrules are in sharp contact with the matrix, their fine‐grained rims are clearly visible, and the boundaries of the dark inclusions can be easily discerned. Many chondrules in GRO 95577 have textures suggestive of type I chondrules, but the phenocrysts have undergone perfect pseudomorphic replacement by yellow to brownish serpentine‐rich phyllosilicate, with sharp original crystal outlines preserved. The chondrule mesostasis is a green aluminous chlorite‐rich material, most likely a hydration product of the feldspathic mesostasis commonly found in anhydrous type I chondrules. Some chondrules contain magnetite spheres, most likely formed by oxidation of metal. We propose that GRO 95577 be classified as a CR1 chondrite, making it the first known CR1 chondrite and expanding the range of alteration conditions on the CR parent body.     

Meteorites from the Nullarbor Region,Western Australia: II. Recovery and classification of 34 new meteorite finds from the Mundrabilla,Forrest, Reid and Deakin areas

Abstract— The discovery of 34 new stony meteorites is reported from those areas of the Nullarbor Region, Western Australia named after Mundrabilla, Forrest, Reid and Deakin sidings on the Trans Australian Railway line. The recoveries include 15 H-, and 15 L-group equilibrated (types 4–6) ordinary chondrites, two distinct H3 chondrites (Mundrabilla 003 and Forrest 003), a genomict H-group chondrite breccia (Reid 011) comprising types 3–6, and one structurally anomalous chondrite (Deakin 001). Seventy-eight distinct meteorites are now known from the region.     

Modal abundances of CAIs: Implications for bulk chondrite element abundances and fractionations

Abstract— Modal abundances of Ca,Al‐rich inclusions (CAIs) are poorly known and reported data scatter across large ranges. CAIs are Poisson distributed, and if only small areas (<1000 mm²) are studied, the data are probably not representative of the true CAI modal abundances, explaining their reported large scatter in a single chondrite group. We combine reported CAI modal abundances and our own set, and present a complete list of CAI modal abundances in carbonaceous chondrites. This includes (in area%): CV: 2.98, CM: 1.21, Acfer 094: 1.12, CO: 0.99, CK/CV (Ningqiang and Dar al Gani [DaG] 055): 0.77, CK: 0.2, CR: 0.12 and CB: 0.1. CAIs are Poisson distributed and if only small areas are studied, the data are probably not representative of the true CAI modal abundances, Carbonaceous chondrites have excess bulk Al concentrations when compared to the CI‐chondritic value. We find a correlation between this excess and CAI modal abundances and conclude that the excess Al was delivered by CAIs. The excess Al is only a minor fraction (usually ?10 rel%, but 25 rel% in case of CVs) of the bulk chondrite Al and cannot have contributed much ²⁶Al to heat the chondrite parent body. Ordinary, enstatite, R and K chondrites have an Al deficit relative to CI chondrites and only very low CAI modal abundances, if any are present at all. Carbonaceous chondrites also had an initial Al deficit if the contribution of Al delivered by CAIs is subtracted. Therefore all chondrites probably lost a refractory rich high‐T component. Only minor amounts of CAIs are present in the matrix or have been present in the chondrule precursor aggregates. Most CAI size distributions contain more than one size population, indicating that CAIs from within a single meteorite group had different origins.     

Effect of polychromatic X‐ray microtomography imaging on the amino acid content of the Murchison CM chondrite

X‐ray microcomputed tomography (μCT) is a useful means of characterizing cosmochemical samples such as meteorites or robotically returned samples. However, there are occasional concerns that the use of μCT may be detrimental to the organic components of a chondrite. Small organic compounds such as amino acids comprise up to ~10% of the total solvent extractable carbon in CM carbonaceous chondrites. We irradiated three samples of the Murchison CM carbonaceous chondrite under conditions akin to and harsher than those typically used during typical benchtop X‐ray μCT imaging experiments to determine if detectable changes in the amino acid abundance and distribution relative to a nonexposed Murchison control sample occurred. After subjecting three meteorite samples to ionizing radiation dosages between ~300 Gray (Gy) and 3 kGy with bremstrahlung X‐rays, we analyzed the amino acid content of each sample. Within sampling and analytical errors, we cannot discern differences in the amino acid abundances and amino acid enantiomeric ratios when comparing the control samples (nonexposed Murchison) and the irradiated samples. We conclude that a polychromatic X‐ray μCT experiment does not alter the abundances of amino acids to a degree greater than how well those abundances are measured with our techniques and therefore any damage to amino acids is minimal.     

Re‐examining the role of chondrules in producing the elemental fractionations in chondrites

Abstract— The matrices of all primitive chondrites contain presolar materials (circumstellar grains and interstellar organics) in roughly CI abundances, suggesting that all chondrites accreted matrix that is dominated by a CI‐like component. The matrix‐normalized abundances of the more volatile elements (condensation temperatures <750–800 K) in carbonaceous and ordinary chondrites are also at or slightly above CI levels. The modest excesses may be due to low levels of these elements in chondrules and associated metal. Subtraction of a CI‐like matrix component from a bulk ordinary chondrite composition closely matches the average composition of chondrules determined by instrumental neutron activation analysis (INAA) if some Fe‐metal is added to the chondrule composition. Measured matrix compositions are not CI‐like. Sampling bias and secondary redistribution of elements may have played a role, but the best explanation is that ?10–30% of refractory‐rich, volatile depleted material was added to matrix. If most of the more volatile elements are in a CI‐dominated matrix, the major and volatile element fractionations must be largely carried by chondrules. There is both direct and indirect evidence for evaporation during chondrule formation. Type IIA and type B chondrules could have formed from a mixture of CI material and material evaporated from type IA chondrules. The Mg‐Si‐Fe fractionations in the ordinary chondrites can be reproduced with the loss of type IA chondrule material and associated metal. The loss of evaporated material from the chondrules could explain the volatile element fractionations. Mechanisms for how these fractionations occurred are necessarily speculative, but two possibilities are briefly explored.     

Which fireballs are meteorites? A study of the Prairie Network photographic meteor data

Plausible meteorite mass distributions imply that in the Prairie Network data there must be many fainter fireballs produced by meteorites with physical properties that, except for mass, are very similar to the recovered ordinary chondrite (H5) Lost City. Four criteria are proposed for identifying these other meteorites among the fireballs. These are: deceleration to final velocity ≤8 km/sec; a photometric mass/dynamic mass ratio within a factor of 2 of that of Lost City, agreement of the observed and theoretical single body end heights (calculated using dynamic mass), and a lightcurve no more irregular than those of the three recovered fireballs. These criteria can be related to the PE criterion of Ceplecha and McCrosky, but include a wider range of observational data, and also differ from the PE criterion in avoiding inclusion of data not helpful to the particular problem of identifying ordinary chondrite fireballs. By use of our criteria, 27 Prairie Network fireballs are identified as being meteorites comparable to or greater in strength and density to Lost City, most of these should be ordinary chondrites. The orbital element distributions of these objects span a wide range, include those of recovered fireballs, and show that the 4.0-AU aphelion of the Pribram meteorite is not unusually large. Perihelia are concentrated near 1.0 AU, in agreement with previous inferences from time-of-fall and radiant distributions, demonstrating the usefulness of these data based on visual observations.     

Thermally metamorphosed carbonaceous chondrites from data for thermally mobile trace elements

Abstract— We report radiochemical neutron activation analysis (RNAA) data for U, Co, Au, Sb, Ga, Rb, Cs, Se, Ag, Te, Zn, In, Bi, Tl, and Cd (ordered by increasing ease of vaporization and loss from the Murchison CM2 chondrite during open-system heating) in nine Antarctic C2 and C3 chondrites. These meteorites exhibit properties (obtained by reflectance spectroscopy, O isotopic mass spectrometry and/or mineralogy-petrology) suggesting thermal metamorphism in their parent bodies. Five of these meteorites (Asuka (A) 881655, Yamato (Y) 793495, Y-790992, Pecora Escarpment (PCA) 91008, and Y-86789—paired with Y-86720) exhibit significant depletion of the most thermally mobile 1–5 trace elements, which is consistent with open-system loss during extended parent-body heating (under conditions duplicated by week-long heating of the Murchison C2 chondrite, heated at 500–700 °C in a low-pressure (initially 10^?5atm) H₂ atmosphere). From earlier data, three other C3 chondrites—Allan Hills (ALH) 81003, ALH 85003, and Lewis Cliffs (LEW) 85332—show significant Cd depletion. Nine additional C2 and C3 chondrites show no evidence of mobile trace element depletion—including Y-793321, which by all other criteria was mildly metamorphosed thermally. Either metamorphism of these nine meteorites occurred under closed conditions and/or alteration took place under such mild conditions that even Cd could not be lost. The RNAA data suggest that 10 of the 46 Antarctic carbonaceous chondrites (including 4 of 37 from Victoria Land and 6 of 9 from Queen Maud Land) exhibit open-system loss of at least some thermally mobile trace elements by heating in their parent bodies, whereas none of the 25 non-Antarctic falls experienced this. These results are consistent with the idea that the Antarctic sampling of near-Earth material differs from that being sampled today.     

Coolidge and Loongana 001: A new carbonaceous chondrite grouplet

Abstract— Petrographic and bulk compositional data suggest the existence of a new grouplet of carbonaceous chondrites consisting of Coolidge and Loongana 001. Coolidge is a carbonaceous chondrite find from Kansas, USA, previously considered a metamorphosed CV chondrite. Loongana 001 is a recent find from Western Australia. It has a high matrix/chondrule modal abundance ratio, 1–2 vol% refractory inclusions and high refractory lithophile abundance ratios (～1.35x CI), indicating that it is a carbonaceous chondrite. Coolidge and Loongana 001 have many compositional and petrographic similarities. They have refractory element abundances in the range of CV chondrites, significantly higher than those in the CR chondrites. They have similar volatile element abundance patterns showing low volatile element abundances relative to both CR and CV chondrites. Coolidge and Loongana 001 have similar chondrule dimensions and shapes, oxidation states and opaque mineral assemblages. They are also similar in petrologic type (3.8–4) and shock stage (S2). Although both Coolidge and Loongana 001 may be related to the CV clan, they are not CV chondrites, nor are they formed by metamorphism of a CV precursor. They are distinctly different in composition from CV chondrites and their chondrules are smaller and have a much lower abundance of coarse-grained chondrule rims. Coolidge and Loongana 001 constitute a distinct carbonaceous chondrite grouplet.     

Effect of a synchrotron X‐ray microtomography imaging experiment on the amino acid content of a CM chondrite

X‐ray microcomputed tomography and synchrotron X‐ray microcomputed tomography (μCT) are becoming popular tools for the reconnaissance imaging of chondrites. However, there are occasional concerns that the use of μCT may be detrimental to organic components of a chondrite. Soluble organic compounds represent ~2–10% of the total solvent extractable carbon in CI and CM carbonaceous chondrites and amino acids are among the most abundant compounds in the soluble organic fraction. We irradiated two samples of the Murchison CM2 carbonaceous chondrite under conditions slightly harsher (increased beam exposure time) than those typically used for x‐ray μCT imaging experiments to determine if detectable changes in the amino acid abundance and distribution relative to a nonexposed control sample occurred. After subjecting two meteorite portions to ionizing radiation dosages of 1.1 kiloGray (kGy) and 1.2 kGy with 48.6 and 46.6 keV monochromatic X‐rays, respectively, we analyzed the amino acid content of each sample. Within analytical errors, we found no differences in the amino acid abundances or enantiomeric ratios when comparing the control samples (nonexposed Murchison) and the irradiated samples. We show with calculations that any sample heating due to x‐ray exposure is negligible. We conclude that a monochromatic synchrotron X‐ray μCT experiment at beamline 13‐BM‐D of the Advanced Photon Source, which imparts ~1 kGy doses, has no detectable effect on the amino acid content of a carbonaceous chondrite. These results are important for the initial reconnaissance of returned samples from the OSIRIS‐REx and Hayabusa 2 asteroid sample return missions.     

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.     

Niobium and tantalum in carbonaceous chondrites: Constraints on the solar system and primitive mantle niobium/tantalum,zirconium/niobium,and niobium/uranium ratio

Abstract— We have determined Nb, Y, and Zr abundances in the carbonaceous chondrites Orgueil (CI), Murray (CM2), Murchison (CM2), Allende (CV3), and Karoonda (CK4), and in the eucrites, Pasamonte and Juvinas, by a recently developed spark source mass spectrometric technique using multiple ion counting (MIC‐SSMS). The abundance of Ta was determined in the same meteorites by radiochemical neutron activation analysis (RNAA). Precision of the MIC‐SSMS and RNAA techniques is ～3% and ≤ 5%, respectively. The new abundances for CI chondrites are: Nb = 0.247, Ta = 0.0142, Zr = 3.86, Y = 1.56 μg/g; or 0.699, 0.0202, 11.2, and 4.64 atoms/10⁶ Si atoms, respectively. The values agree with earlier compilations, but they are a factor of 2 more precise than earlier analyses. Trace element concentrations in the CM, CV, and CK chondrites are higher than in the CI chondrite Orgueil by about 37, 86, and 120%, respectively, in agreement with the variable absolute contents of refractory lithophile elements in different groups of carbonaceous chondrites. Of particular interest are the chondritic Nb/Ta, Zr/Nb, and Nb/U ratios, because these ratios are important tools for interpreting the chemical evolution of planetary bodies. We obtained Nb/Ta = 17.4 ± 0.5 for the carbonaceous chondrites and the Juvinas‐type eucrites investigated. Though this value is similar to previous estimates, it is much more precise. The same is true for Zr/Nb (15.5 ± 0.2) and Zr/Y (2.32 ± 0.12). In combination with recently published MIC‐SSMS U data for carbonaceous chondrites, we obtained a chondritic Nb/U ratio of 29 ± 2. Because Nb, Ta, Zr, Y, and U are refractory lithophile elements and presumably partitioned into the silicate phase of the Earth during core formation, the elemental ratios may also be used to constrain evolution of the Earth's primitive mantle and, with the more precise determinations fractionation of Nb and Ta during magmatic processes and mantle‐crust interactions, can now be interpreted with greater confidence.     

Highly siderophile and chalcogen element constraints on the origin of components of the Allende and Murchison meteorites

¹⁸⁷Re‐¹⁸⁷Os systematics, abundances of highly siderophile elements (HSE: Re, PGE, and Au), chalcogen elements (Te, Se, and S), and some major and minor elements were determined in physically separated components of the Allende (CV3) and Murchison (CM2) carbonaceous chondrites. Substantial differences exist in the absolute and relative abundances of elements in the components, but the similarity of calculated and literature bulk rock abundances of HSE and chalcogens indicate that chemical complementarity exists among the components, with CI chondrite‐like ratios for many elements. Despite subsequent alteration and oxidation, the overall cosmochemical behavior of most moderately to highly siderophile elements during high‐temperature processing has been preserved in components of Allende at the sampling scale of the present study. The ¹⁸⁷Re‐¹⁸⁷Os systematics and element variations of Allende are less disturbed compared with Murchison, which reflects different degrees of oxidation and alteration of these meteorites. The HSE systematics (with the exception of Au) is controlled by two types of materials: Pd‐depleted condensates and CI chondrite‐like material. Enrichment and heterogeneous distribution of Au among the components is likely the result of hydrothermal alteration. Chalcogen elements are depleted compared with HSE in all components, presumably due to their higher volatility. Small systematic variations of S, Se, and Te in components bear the signature of fractional condensation/partial evaporation and metal–sulfide–silicate partitioning.     

Petrology and bulk chemistry of Yamato‐82094, a new type of carbonaceous chondrite

Carbonaceous chondrites are classified into several groups. However, some are ungrouped. We studied one such ungrouped chondrite, Y‐82094, previously classified as a CO. In this chondrite, chondrules occupy 78 vol%, and the matrix is distinctly poor in abundance (11 vol%), compared with CO and other C chondrites. The average chondrule size is 0.33 mm, different from that in C chondrites. Although these features are similar to those in ordinary chondrites, Y‐82094 contains 3 vol% Ca‐Al‐rich inclusions and 5% amoeboid olivine aggregates (AOAs). Also, the bulk composition resembles that of CO chondrites, except for the volatile elements, which are highly depleted. The oxygen isotopic composition of Y‐82094 is within the range of CO and CV chondrites. Therefore, Y‐82094 is an ungrouped C chondrite, not similar to any other C chondrite previously reported. Thin FeO‐rich rims on AOA olivine and the mode of occurrence of Ni‐rich metal in the chondrules indicate that Y‐82094 is petrologic type 3.2. The extremely low abundance of type II chondrules and high abundance of Fe‐Ni metal in the chondrules suggest reducing condition during chondrule formation. The depletion of volatile elements indicates that the components formed under high‐temperature conditions, and accreted to the parent body of Y‐82094. Our study suggests a wider range of formation conditions than currently recorded by the major C chondrite groups. Additionally, Y‐82094 may represent a new, previously unsampled, asteroidal body.     

Analysis of ordinary chondrites using powder X‐ray diffraction: 1. Modal mineral abundances

Abstract– Powder X‐ray diffraction (XRD) is used to quantify the modal abundances (in wt%) of 18 H, 17 L, and 13 LL unbrecciated ordinary chondrite falls, which represents the complete petrologic range of equilibrated ordinary chondrites (types 4–6). The XRD technique presents an effective alternative to traditional methods for determining modal abundances, such as optical point counting and electron microprobe phase (EMP) mapping. The majority of chondrite powders in this study were previously prepared for chemical characterization from 8 to 20 g of material, which is consistent with the suggested mass (10 g) necessary to provide representative sampling of ordinary chondrites. Olivine and low‐Ca pyroxene are the most abundant phases present, comprising one‐half to three‐fourths of total abundances, while plagioclase, high‐Ca pyroxene, troilite, and metal comprise the remaining XRD‐measured mineralogy. Pigeonite may also be present in some samples, but it is fitted using a high‐Ca pyroxene standard, so exact abundances cannot be measured directly using XRD. Comparison of XRD‐measured abundances with calculated Cross, Iddings, Pirsson, Washington (CIPW) normative abundances indicates that systematic discrepancies exist between these two data sets, particularly in olivine and high‐Ca pyroxene. This discrepancy is attributed to the absence of pigeonite as a possible phase in the CIPW normative mineralogy. Oxides associated with pigeonite are improperly allocated, resulting in overestimated normative olivine abundances and underestimated normative high‐Ca pyroxene abundances. This suggests that the CIPW norm is poorly suited for determining mineralogical modal abundances of ordinary chondrites.     

Iron‐rich aureoles in the CM carbonaceous chondrites Murray,Murchison, and Allan Hills 81002: Evidence for in situ aqueous alteration

Abstract— Iron‐rich aureoles in CM carbonaceous chondrites are previously unidentified domains of aqueously altered matrix material, whose FeO content may exceed that of the surrounding matrix by up to more than 15 wt%. We describe the petrography and mineralogy of these objects in the CM chondrites Murray, Murchison, and Allan Hills (ALH) 81002. The size of Fe‐rich aureoles ranges from a few hundred microns to several millimeters in diameter and appears to be a function of the degree of alteration of the host chondrite. The origin of Fe‐rich aureoles is related to the alteration of large metal grains that has resulted in the formation of characteristic PCP‐rich reaction products that are frequently observed at the centers of the aureoles. This suggests that Fe‐rich aureoles in CM chondrites are the result of the mobilization of Fe from altering metal grains into the matrix. The fact that Fe‐rich aureoles enclose numerous chondritic components such as chondrules, calcium‐aluminum‐rich inclusions (CAIs), and mineral fragments, as well as their radial symmetric appearance, are strong evidence that they formed in situ and that significant directional fluid flow was not involved in the alteration process. This and additional constraints, such as the distribution of S and other elements, as well as the inferred alteration conditions, are consistent with in situ parent‐body alteration. The observations are, however, entirely incompatible with preaccretionary alteration models in which the individual CM chondrite components have experienced diverse alteration histories. The presence of numerous intact aureoles in the brecciated CM chondrites Murray and Murchison further suggests that the alteration occurred largely after brecciation affected these meteorites. Therefore, the progressive aqueous alteration of CM chondrites may not be necessarily coupled to brecciation as has been previously proposed.