Cumberland Falls chondritic inclusions—II. Trace element contents of forsterite chondrites and meteorites of similar redox state

Mineralogic study of black inclusions in the Cumberland Falls enstatite achondrite revealed that they constitute a highly unequilibrated chondritic suite distinct from other chondrite groups. This highly shocked suite, the forsterite (F) chondrites, exhibits mineralogic trends apparently produced during primary nebular condensation and accretion over a broad redox range. We analyzed these samples and possibly related meteorites for Ag, As, Au, Bi, Cd, Co, Cs, Ga, In, Rb, Sb, Se, Te, Tl, U and Zn, trace elements known to yield important genetic information. The results demonstrate the compositional coherence and distinctiveness of the F chondrite suite relative to other chondrites. The Antarctic aubrite, ALH A78113, may include more F chondrite material. Trace element contents do not vary with mineral compositions hence do not reflect redox variations during formation of F chondrite parental matter. Trace element mobilization—during secondary heating episodes in the F chondrite parent or during its disruptive collision with the enstatite meteorite parent body—is not detectable. Chemical trends in F chondrites apparently reflect primary nebular processes. Cosmochemical fractionation of lithophiles from siderophiles and chalcophiles occurred at moderately high temperatures, certainly higher than those existing during formation of primitive carbonaceous, enstatite and ordinary chondrites of petrologic type ≤3.     

The nature,origin and modification of insoluble organic matter in chondrites,the major source of Earth’s C and N

All chondrites accreted ∼3.5 wt.% C in their matrices, the bulk of which was in a macromolecular solvent and acid insoluble organic material (IOM). Similar material to IOM is found in interplanetary dust particles (IDPs) and comets. The IOM accounts for almost all of the C and N in chondrites, and a significant fraction of the H. Chondrites and, to a lesser extent, comets were probably the major sources of volatiles for the Earth and the other terrestrial planets. Hence, IOM was both the major source of Earth’s volatiles and a potential source of complex prebiotic molecules.Large enrichments in D and ¹⁵N, relative to the bulk solar isotopic compositions, suggest that IOM or its precursors formed in very cold, radiation-rich environments. Whether these environments were in the interstellar medium (ISM) or the outer Solar System is unresolved. Nevertheless, the elemental and isotopic compositions and functional group chemistry of IOM provide important clues to the origin(s) of organic matter in protoplanetary disks. IOM is modified relatively easily by thermal and aqueous processes, so that it can also be used to constrain the conditions in the solar nebula prior to chondrite accretion and the conditions in the chondrite parent bodies after accretion.Here we review what is known about the abundances, compositions and physical nature of IOM in the most primitive chondrites. We also discuss how the IOM has been modified by thermal metamorphism and aqueous alteration in the chondrite parent bodies, and how these changes may be used both as petrologic indicators of the intensity of parent body processing and as tools for classification. Finally, we critically assess the various proposed mechanisms for the formation of IOM in the ISM or Solar System.     

Presolar diamond, silicon carbide, and graphite in carbonaceous chondrites: implications for thermal processing in the solar nebula

We have determined abundances of presolar diamond, silicon carbide, graphite, and Xe-P1 (Q-Xe) in eight carbonaceous chondrites by measuring the abundances of noble gas tracers in acid residues. The meteorites studied were Murchison (CM2), Murray (CM2), Renazzo (CR2), ALHA77307 (CO3.0), Colony (CO3.0), Mokoia (CV3_ox), Axtell (CV3_ox), and Acfer 214 (CH). These data and data obtained previously by Huss and Lewis (1995) provide the first reasonably comprehensive database of presolar-grain abundances in carbonaceous chondrites. Evidence is presented for a currently unrecognized Ne-E(H) carrier in CI and CM2 chondrites.After accounting for parent-body metamorphism, abundances and characteristics of presolar components still show large variations across the classes of carbonaceous chondrites. These variations correlate with the bulk compositions of the host meteorites and imply that the same thermal processing that was responsible for generating the compositional differences between the various chondrite groups also modified the initial presolar-grain assemblages. The CI chondrites and CM2 matrix have the least fractionated bulk compositions relative to the sun and the highest abundances of most types of presolar material, particularly the most fragile types, and thus are probably most representative of the material inherited from the sun's parent molecular cloud. The other classes can be understood as the products of various degrees of heating of bulk molecular cloud material in the solar nebula, removing the volatile elements and destroying the most fragile presolar components, followed by chondrule formation, metal-silicate fractionation in some cases, further nebula processing in some cases, accretion, and parent body processing. If the bulk compositions and the characteristics of the presolar-grain assemblages in various chondrite classes reflect the same processes, as seems likely, then differential condensation from a nebula of solar composition is ruled out as the mechanism for producing the chondrite classes. Presolar grains would have been destroyed if the nebula had been completely vaporized. Our analysis shows that carbonaceous chondrites reflect all stages of nebular processing and thus are no more closely related to one another than they are to ordinary and enstatite chondrites.     

Deuterium enrichments in chondritic macromolecular material—Implications for the origin and evolution of organics, water and asteroids

Here we report the elemental and isotopic compositions of the insoluble organic material (IOM) isolated from several previously unanalyzed meteorites, as well as the reanalyses of H isotopic compositions of some previously measured samples (Alexander et al., 2007). The IOM in ordinary chondrites (OCs) has very large D enrichments that increase with increasing metamorphism and decreasing H/C, the most extreme δD value measured being almost 12,000‰. We propose that such large isotopic fractionations could be produced in the OC parent bodies through the loss of isotopically very light H₂ generated when Fe was oxidized by water at low temperatures (<200 °C). We suggest that similar isotopic fractionations were not generated in the IOM of CV and CO chondrites with similar metamorphic grades and IOM H/C ratios because proportionately less water was consumed during metamorphism, and the remaining water buffered the H isotopic composition of the IOM even a H was being lost from it.Hydrogen would also have been generated during the alteration of CI, CM and CR carbonaceous chondrites. The IOM in these meteorites exhibit a considerable range in isotopic compositions, but all are enriched in D, as well as ¹⁵N, relative to terrestrial values. We explore whether these enrichments could also have been produced by the loss of H₂, but conclude that the most isotopically anomalous IOM compositions in meteorites from these groups are probably closest to their primordial values. The less isotopically anomalous IOM has probably been modified by parent body processes. The response of IOM to these processes was complex and varied, presumably reflecting differences in conditions within and between parent bodies.The D enrichments associated with H₂ generation, along with exchange between D-rich IOM and water in the parent bodies, means that it is unlikely that any chondrites retain the primordial H isotopic composition of the water ice that they accreted. The H isotopic compositions of the most water-rich chondrites, the CMs and CIs, are probably the least modified and their compositions (δD ? −25‰) suggest that their water did not form at large radial distances from the Sun where ice is predicted to be very D-rich. Yet models to explain the O isotopic composition of inner Solar System bodies require that large amounts of ice were transported from the outer to the inner Solar System.     

An Fe isotope study of ordinary chondrites

The Fe isotope composition of ordinary chondrites and their constituent chondrules, metal and sulphide grains have been systematically investigated. Bulk chondrites fall within a restricted isotopic range of <0.2‰ δ⁵⁶Fe, and chondrules define a larger range of >1‰ (−0.84‰ to 0.21‰ relative to the IRMM-14 Fe standard). Fe isotope compositions do not vary systematically with the very large differences in total Fe concentration, or oxidation state, of the H, L, and LL chondrite classes. Similarly, the Fe isotope compositions of chondrules do not appear to be determined by the H, L or LL classification of their host chondrite. This may support an origin of the three ordinary chondrite groups from variable accretion of identical Fe-bearing precursors.A close relationship between isotopic composition and redistribution of Fe during metamorphism on ordinary chondrite parent bodies was identified; the largest variations in chondrule compositions were found in chondrites of the lowest petrologic types. The clear link between element redistribution and isotopic composition has implications for many other non-traditional isotope systems (e.g. Mg, Si, Ca, Cr). Isotopic compositions of chondrules may also be determined by their melting history; porphyritic chondrules exhibit a wide range in isotope compositions whereas barred olivine and radial pyroxene chondrules are generally isotopically heavier than the ordinary chondrite mean. Very large chondrules preserve the greatest heterogeneity of Fe isotopes.The mean Fe isotope composition of bulk ordinary chondrites was found to be −0.06‰ (±0.12‰ 2 SD); this is isotopically lighter than the terrestrial mean composition and all other published non-chondritic meteorite suites e.g. lunar and Martian samples, eucrites, pallasites, and irons. Ordinary chondrites, though the most common meteorites found on Earth today, were not the sole building blocks of the terrestrial planets.     

陨石氧同位素组成及其地学意义

介绍了各类陨石氧同位素组成的特点,对陨石氧同位素组成的主要成因观点进行了评述,结合地球的原始物质组成,讨论了陨石氧同位素组成的地球科学意义。     

对南极类C1陨石成因和星云水化作用范围的几点看法

南极陨石的研究发现，有几个碳质球粒陨石富含与ＣＩ陨石类似的含水层状硅酸盐集合体及其角砾，其氧同位素比值也与ＣＩ接近，因而称之为类Ｃ１陨石。类Ｃ１陨石与Ｃ１陨石的区别是：类Ｃ１陨石中的含水层状硅酸盐既以基质的形式产出，也出现在球粒中；类Ｃ１陨石中含有球粒及有关组分，如球粒碎块、矿物集合体等。每个陨石中所含这些组分的数量不同，其矿物的成分也差别很大，从而说明它们形成的星云环境不同。因此笔者认为类Ｃ１陨     

对南极类C1陨石成因和星云水化作用范围的几点看法

南极陨石的研究发现，有几个碳质球粒陨石富含与Ｃ１陨石类似的含水层状硅酸盐集合体及其角砾．其氧同位素比值也与Ｃ１接近，因而称之为类Ｃ１陨石。类Ｃ１陨石与Ｃ１陨石的区别是：类Ｃ１陨石中的含水层状硅酸盐既以基质的形式产出，也出现在球粒中；类Ｃ１陨石中含有球粒及有关组分，如球粒碎块、矿物集合体等。每个陨石中所含这些组分的数量不同，其矿物的成分也差别很大，从而说明它们形成的星云环境不同。因此笔者认为类Ｃ１陨石可能是小行星区星云盘外层的星云凝聚物受到不同程度水化作用后吸积形成的陨石。     

太阳星云凝聚过程的岩石学模型：（Ⅱ）非球陨石、C1陨石及类C1陨石的凝聚成因和小行星区星云凝聚作用

综述了非球陨石（铁陨石，石铁陨石和无球粒陨石）在成分结构方面的非分异成因证据，推断其成因是：星云盘中心层中的星云发生气－液凝聚作用形成的熔滴，在较高温度下彼此合并形成了较大熔体，熔体固化后形成该类陨石母体。根据Ｃ１陨石不含球粒和其它成分特征，推断它们是星云只发生气－固凝聚作用的产物。对近年来新发现的一些特殊成分的碳质球粒陨石进行了综合分析，暂定名为类Ｃ１陨石。通过类Ｃ１陨石与其它球粒陨石及Ｃ１陨石成分结构特征的对比，推断它们是星云盘边缘层星云发生气－液－固和气－固联合凝聚作用，同时发生水化作用的产物。最后，在对所有陨石凝聚成因进行解释的基础上，建立了小行星区星云凝聚模型。     

陨石含水矿物成因评述和地球水来源的探讨

简要介绍了球粒陨石中含水矿物的种类和主要特点，根据陨石中含水矿物与无水矿物，有机质的关系，太阳星云凝聚模型中有关水蒸汽与无水矿物反应的理论，以及有关的同位素资料的综合分析，推断形成含水矿物的水化作用是太阳星云凝聚作用的一个阶段，通过不同类型球粒陨石氧同位素组成和含水矿物数量的比较，论证了太阳星云盘中发生水作用的范围，从而对地球水的来源进行了讨论。     

Chemical studies of L chondrites—II. Shock-induced trace element mobilization

Previous studies of chondrites heated in the laboratory for extended periods under conditions approximating those in shock-heated collisional debris indicate that Au, Co, Se, Ga, Rb, Cs, Te, Bi, In, Ag, Zn, Tl and Cd progress in mobility. We report data for these 13 trace elements in 14 L4–6 chondrites of established shock history and discuss these and 13 additional chondrites studied earlier. Trace element contents vary with petrologic type, $\text{S}\text{Fe}$ sub-group and shock history, the last dominating strongly. Absolute abundances and interelement relationships for the 6 or 7 most mobile elements vary with degree of shock-loading (i.e. residual temperatures) established from mineralogic/petrologic study. A tertiary process, shock-heating, previously known to have affected radiogenic ⁴⁰Ar and/or ⁴He in meteorites but not other elements, apparently was at least as effective as other open-system processes (secondary [parent body] and primary [nebular and/or accretionary] episodes) in establishing mobile trace element contents of L chondrites and probably others. If conditions during early genetic episodes are to be deduced from compositional information, shocked meteorites should be avoided or effects of later processes should be compensated for.     

陨石分类研究进展及其地学意义

近40年来陨石分类学经历了3个发展阶段，60－70年代，由根据陨石的矿物结构的分类方法发展为球粒陨石的化学一岩石学分类法和铁陨石的化学群分类法；70－80年代，提出了分异型陨石和未分异型陨石的概念，球粒陨石被认为是未分异型陨石，而其它陨石（铁陨石，石铁陨石和无球粒陨石）大多被划入分异型陨石，80－90年代以来，陨石氧同位素组成成为了陨石成因分类的一个主要依据，使陨石分类学进入了一个新的成因分类阶段，作者对80－90年代以来新确立的R群，K小群，CR群和CK群球粒陨石，以及根据氧同位素划分出的原始型无球粒陨石系列：A－L无球粒陨石，Winonaites无球粒陨石和Brachinites无球粒陨石进行了介绍，笔者对陨石研究和陨石分类学的发展在估算地球整体成分，探讨地球成因和早期演化历史方面的重要意义进行了说明，并建议地球科学家应对陨石学和陨石分类的发展现状给以关注。     

Heavily fractionated noble gases in an acid residue from the Klein Glacier 98300 EH3 chondrite

Noble gases were measured both in bulk samples (stepped pyrolysis and total extraction) and in a HF/HCl residue (stepped pyrolysis and combustion) from the Klein Glacier (KLE) 98300 EH3 chondrite. Like the bulk meteorite and as seen in previous studies of bulk type 3 E chondrites (“sub-Q”), the acid residue contains elementally fractionated primordial noble gases. As we show here, isotopically these are like those in phase-Q of primitive meteorites, but elementally they are heavily fractionated relative to these. The observed noble gases are different from “normal” Q noble gases also with respect to release patterns, which are similar to those of Ar-rich noble gases in anhydrous carbonaceous chondrites and unequilibrated ordinary chondrites (with also similar isotopic compositions). While we cannot completely rule out a role for parent body processes such as thermal and shock metamorphism (including a later thermal event) in creating the fractionated elemental compositions, parent body processes in general seem not be able to account for the distinct release patterns from those of normal Q noble gases. The fractionated gases may have originated from ion implantation from a nebular plasma as has been suggested for other types of primordial noble gases, including Q, Ar-rich, and ureilite noble gases. With solar starting composition, the corresponding effective electron temperature is about 5000 K. This is lower than inferred for other primordial noble gases (10,000-6000 K). Thus, if ion implantation from a solar composition reservoir was a common process for the acquisition of primordial gas, electron temperatures in the early solar system must have varied spatially or temporally between 10,000 and 5000 K.Neon and xenon isotopic ratios of the residue suggest the presence of presolar silicon carbide and diamond in abundances lower than in the Qingzhen EH3 and Indarch EH4 chondrites. Parent body processes including thermal and shock metamorphism and a late thermal event also cannot be responsible for the low abundances of presolar grains. KLE 98300 may have started out with smaller amounts of presolar grains than Qingzhen and Indarch.     

Compositional diversity in insoluble organic matter in type 1, 2 and 3 chondrites as detected by infrared spectroscopy

Insoluble organic matter (IOM) isolated from 22 carbonaceous and ordinary chondrites spanning a wide range of groups and petrologic types were analyzed using Fourier transform infrared spectroscopy (FTIR). Based on common IR spectral features, it is observed that IOM falls into 4 molecularly distinct groups (designated here as A through D). Spectral group A includes type 1 and 2 chondrites and exhibits intense aliphatic C-H and carboxyl vibrational peaks. Spectral group B includes the least metamorphosed type 3 chondrites and Tagish Lake, and exhibits weaker aliphatic and carboxyl vibrational intensity. Spectral groups C and D include metamorphosed type ?3.1 chondrites and a heated CM chondrite. The carbonyl stretching features in spectral groups C and D differ from that in spectral groups A and B and from each other. In spectral group C, the carbonyl stretching is assigned to cyclic unsaturated lactones; in spectral group D carbonyl exists predominantly in the form of unsaturated ketone moieties. Both spectral groups C and D have a relatively narrow band structure around 1210 cm⁻¹ (assigned to aromatic skeletal modes) as compared with spectral groups A and B, which is consistent with the formation of more condensed aromatics by extensive thermal metamorphism. The differences in carbonyl structures in spectral groups C and D are not the result of different effective metamorphic temperatures, rather these differences likely result from variation in the activity of water and oxygen at different stages of parent body metamorphism. Such environmental variations must be local phenomena in the parent bodies as there is no correlation between spectral grouping and chondrite class or group.     

Effects of secondary alteration on the composition of free and IOM-derived monocarboxylic acids in carbonaceous chondrites

Monocarboxylic acids (MCAs) are important astrobiologically because they are often the most abundant soluble compounds in carbonaceous chondrites (CCs) and are potential synthetic end products for many biologically important compounds. However, there has been no systematic study on the effect of parent body alteration on molecular and isotopic variability of MCAs. Since MCAs in meteorites are dominated by low molecular weight (C1-C8), highly volatile compounds, their distributions are likely to be particularly sensitive to secondary alteration processes. In contrast, the aliphatic side chains of insoluble organic matter (IOM) in CCs, whose composition has been shown to be closely related to the MCAs, may be far more resistant to secondary alteration. In the present study, we determined the distributions and isotopic ratios of free and IOM-derived MCAs in six carbonaceous chondrites with a range of classifications: Murchison (CM2), EET 87770 (CR2), ALH 83034 (CM1), ALH 83033 (CM2), MET 00430 (CV3) and WIS 91600 (C2). We compare mineralogical and petrological characteristics to the MCAs distributions to better define the processes leading to the synthesis and alteration of meteoritic MCAs. Our results show that aqueous and especially thermal alteration in the parent bodies led to major loss of free MCAs and depletion of straight relative to branched chain compounds. However, the MCAs derived from aliphatic side chains of IOM are well preserved despite of secondary alterations. The molecular and isotopic similarities of IOM-derived MCAs in different chondrite samples indicate very similar synthetic histories for organic matter in different meteorites.     

Cumberland Falls chondritic inclusions: Mineralogy/petrology of a forsterite chondrite suite

As previously found for a chondritic inclusion of unknown affinity, mineralogic and petrologic properties of 9 inclusions in the Cumberland Falls enstatitc achondrite are primitive members of the forsterite (F) chondrite group, hitherto defined by 4 meteorites of similar redox state. The inclusions define a primitive suite with properties indicating 8 as F3 and one of even lower petrologic type. The abundant minerals include: low-Ca pyroxene, olivine, plagioclase, kamacite, taenite, schreibersite, troilite, ferroan alabandite and daubreelite. Diopside, oldhamite and a Ti-rich sulfide are present in one or two inclusions. Petrologic textures and jadeitic pyroxene, hitherto unidentified in meteorites, indicate substantial degree of shock. The inclusions acquired their chemical characteristics during nebular condensation and accretion over a broad redox range (metal-silicate trends in them verify Prior's Rules): their parent body later impacted the enstatite meteorite parent body. During impact, the inclusions were shocked and incorporated with enstatite achondrite host as a breccia that would become Cumberland Falls.     

Comparative stable isotope geochemistry of Ni, Cu, Zn, and Fe in chondrites and iron meteorites

High-precision Ni isotopic variations are reported for the metal phase of equilibrated and unequilibrated ordinary chondrites, carbonaceous chondrites, iron meteorites, mesosiderites, and pallasites. We also report new Zn and Cu isotopic data for some of these samples and combine them with literature Fe, Cu, and Zn isotope data to constrain the fractionation history of metals during nebular (vapor/solid) and planetary (metal/sulfide/silicate) phase changes.The observed variations of the ⁶²Ni/⁵⁸Ni, ⁶¹Ni/⁵⁸Ni, and ⁶⁰Ni/⁵⁸Ni ratios vary linearly with mass difference and define isotope fractionation lines in common with terrestrial samples. This implies that Ni was derived from a single homogeneous reservoir. While no ⁶⁰Ni anomaly is detected within the analytical uncertainties, Ni isotopic fractionation up to 0.45‰ per mass-difference unit is observed. The isotope compositions of Ni and Zn in chondrites are positively correlated. We suggest that, in ordinary chondrites, exchange between solid phases, in particular metal and silicates, and vapor followed by mineral sorting during accretion are the main processes controlling these isotopic variations. The positive correlation between Ni and Zn isotope compositions contrasts with a negative correlation between Ni (and Zn) and Cu isotope compositions, which, when taken together, do not favor a simple kinetic interpretation. The observed transition element similarities between different groups of chondrites and iron meteorites are consistent with the genetic relationships inferred from oxygen isotopes (IIIA/pallasites and IVA/L chondrites). Copper is an exception, which we suggest may be related to separate processing of sulfides either in the vapor or during core formation.     

Dark inclusions in CO3 chondrites: new indicators of parent-body processes

A petrographic and scanning electron microscopic study of the four CO3 chondrites Kainsaz, Ornans, Lancé, and Warrenton reveals for the first time that dark inclusions (DIs) occur in all the meteorites. DIs are mostly smaller in size than those reported from CV3 chondrites. They show evidence suggesting that they were formed by aqueous alteration and subsequent dehydration of a chondritic precursor and so probably have a formation history similar to that of DIs in CV3 chondrites. DIs in the CO3 chondrites consist mostly of fine-grained, Fe-rich olivine and can be divided into two types on the basis of texture. Type I DIs contain rounded, porous aggregates of fine grains in a fine-grained matrix and have textures suggesting that they are fragments of chondrule pseudomorphs. Veins filled with Fe-rich olivine are common in type I DIs, providing evidence that they experienced aqueous alteration on the parent body. Type II DIs lack rounded porous aggregates and have a matrix-like, featureless texture. Bulk chemical compositions of DIs and mineralogical characteristics of olivine grains in DIs suggest that these two types of DIs have a close genetic relationship.The DIs are probably clasts that have undergone aqueous alteration and subsequent dehydration at a location different from the present location in the meteorites. The major element compositions, the mineralogy of metallic phases, and the widely dispersed nature of the DIs suggest that their precursor was CO chondrite material. The CO parent body has been commonly regarded to have been dry, homogeneous, and unprocessed. However, the DIs suggest that the CO parent body was a heterogeneous conglomerate consisting of water-bearing regions and water-free regions and that during asteroidal heating, the water-bearing regions were aqueously altered and subsequently dehydrated. Brecciation may also have been active in the parent body.The DIs and the matrices are similarly affected by thermal metamorphism in their own host CO3 chondrites (petrologic subtypes 3.1 to 3.6), but the degree of the secondary processing (aqueous alteration and subsequent dehydration) of the DIs has no apparent correlation with the petrologic grades of the host chondrites. These observations suggest that the DIs had been incorporated into the host chondrites before the thermal metamorphism took place and that the secondary processes that affected the DIs largely occurred before the thermal metamorphism.     

陨石学及天体化学研究某些新进展

陨石是来自含气体-尘粒的太阳早期星云盘凝聚和吸积的原始物质,大多数原始物质因吸积后的作用过程而改变（如月球、地球及火星样品）,但有一些却完整的保存下来（如球粒陨石或球粒陨石中的难熔包体）。这些原始的物质通常依据同位素丰度特征来识别,依据其矿物-岩石学特征和成因可将已知的陨石划分许多更小的类型。陨石学及天体化学的新近进展包括：新近识别的陨石群;发现新类型球粒陨石及行星际尘粒中发现前太阳和星云组分;利用短寿命放射性核素完善了早期太阳系年代学;洞察宇宙化学丰度、分馏作用及星云源区及通过次生母体的作用过程阐释星云和前星云的记录。本文概述了早期太阳系内从星云到陨石的演化过程。依据这些资料,对早期太阳系所经历的多种核合成的输入、瞬时加热事件与星云动力学有一些新的认识,以及认识到小星子和行星体系的演化比以前预期的更快速。     

Multiple parent bodies of polymict brecciated meteorites

In three brecciated meteorites, Bencubbin, Cumberland Falls and Plainview, the oxygen isotopic compositions of different rock types within each meteorite were determined to seek genetic relationships between them. In all cases the isotopic compositions are not consistent with derivation from a single parent body. There is no evidence that chondrites and achondrites could be derived from a common parent body. The chondritic inclusions in Bencubbin and Cumberland Falls cannot be identified with any of the ordinary chondritic meteorites. The carbonaceous chondritic fragments in Bencubbin are smilar to, but not identical with, C2 meteorites. The achondritic portion of Bencubbin has a very unusual isotopic composition, which, along with its close relative Weatherford, sets it in a class distinctly apart from other achondrites. Lithic fragments in brecciated meteorites provide a wider range of rock types than is represented by known macroscopic meteorites. Collisions between some meteorite parent bodies were of sufficiently low velocity that fragments of both are preserved in breccias.