Axtell,a new CV3 chondrite find from Texas

Abstract— We describe a previously unreported meteorite found in Axtell, Texas, in 1943. Based on the mineralogical composition and texture of its matrix and the sizes and abundance of chondrules, we classify it as a CV3 carbonaceous chondrite. The dominant opaque phase in the chondrules is magnetite, and that in refractory inclusions is Ni-rich NiFe metal (awaruite). Axtell, therefore, belongs to the oxidized subgroup of CV3 chondrites, although unlike Allende it escaped strong sulfidation. The meteorite bears a strong textural resemblance to Allende, and its chondrule population and matrix appear to be quite similar to those of Allende, but its refractory inclusions, thermoluminescence properties, and cosmogenic ⁶⁰Co abundances are not. Our data are consistent with a terrestrial age for Axtell of ～100 years and a metamorphic grade slightly lower than that of Allende.     

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.     

Shape,metal abundance,chemistry, and origin of chondrules in the Renazzo (CR) chondrite

Abstract— We used synchrotron X‐ray microtomography to image in 3‐dimensions (3D) eight whole chondrules in a ?1 cm³piece of the Renazzo (CR) chondrite at ?17 μm per volume element (voxel) edge. We report the first volumetric (3D) measurement of metal/silicate ratios in chondrules and quantify indices of chondrule sphericity. Volumetric metal abundances in whole chondrules range from 1 to 37 volume % in 8 measured chondrules and by inspection in tomography data. We show that metal abundances and metal grain locations in individual chondrules cannot be reliably obtained from single random 2D sections. Samples were physically cut to intersect representative chondrules multiple times and to verify 3D data. Detailed 2D chemical analysis combined with 3D data yield highly variable whole‐chondrule Mg/Si ratios with a supra‐chondritic mean value, yet the chemically diverse, independently formed chondrules are mutually complementary in preserving chondritic (solar) Fe/Si ratios in the aggregate CR chondrite. These results are consistent with localized chondrule formation and rapid accretion resulting in chondrule + matrix aggregates (meteorite parent bodies) that preserve the bulk chondritic composition of source regions.     

A database of chondrite analyses including platinum group elements,Ni, Co,Au, and Cr: Implications for the identification of chondritic projectiles

Abstract— Siderophile elements have been used to constrain projectile compositions in terrestrial and lunar impact melt rocks. To obtain a better knowledge of compositional differences between potential chondritic projectile types, meteorite analyses of the elements Ru, Rh, Pd, Os, Ir, Pt, Cr, Co, Ni, and Au were gathered into a database. The presented compilation comprises 806 analyses of 278 chondrites including new ICP‐MS analyses of Allende and two ordinary chondrites. Each data set was evaluated by comparing element ratios of meteorites from the same chondrite group. Characteristic element abundances and ratios were determined for each group. Features observed in the element abundance patterns can be linked directly to the presence of certain components, such as the abundance of refractory elements Os, Ir, and Ru correlating with the occurrence of refractory inclusions in CV, CO, CK, and CM chondrites. The refined characteristic element ratios appear to be representative not only for meteorites, but also for related asteroidal bodies. Chondrite element ratios were compared to previously published values from impact melt rocks of the Popigai and Morokweng impact structures confirming that an identification of the specific type of projectile (L and LL chondrite, respectively) is possible. The assessment for Morokweng is supported by the recent discovery of an LL chondrite fragment in the impact melt rocks. Ultimately, the database provides valuable information for understanding processes in the solar nebula as they are recorded in chondrites. A new type of complementarity between element patterns of CK and EH chondrites is suggested to be the result of condensation, redox, and transportation processes in the solar nebula.     

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.     

Pb isotopic age of the Allende chondrules

Abstract— We have studied Pb‐isotope systematics of chondrules from the oxidized CV3 carbonaceous chondrite Allende. The chondrules contain variably radiogenic Pb with a ²⁰⁶Pb/²⁰⁴Pb ratio between 19.5–268. Pb‐Pb isochron regression for eight most radiogenic analyses yielded the date of 4566.2 ± 2.5 Ma. Internal residue‐leachate isochrons for eight chondrule fractions yielded consistent dates with a weighted average of 4566.6 ± 1.0 Ma, our best estimate for an average age of Allende chondrule formation. This Pb‐Pb age is consistent with the range of model ²⁶Al‐²⁶Mg ages of bulk Allende chondrules reported by Bizzarro et al. (2004) and is indistinguishable from Pb‐Pb ages of Ca‐Al‐rich inclusions (CAIs) from CV chondrites (4567.2 ± 0.6 Ma) (Amelin et al. 2002) and the oldest basaltic meteorites. We infer that chondrule formation started contemporaneously with or shortly after formation of CV CAIs and overlapped in time with formation of the basaltic crust and iron cores of differentiated asteroids. The entire period of chondrule formation lasted from 4566.6 ± 1.0 Ma (Allende) to 4564.7 ± 0.6 Ma (CR chondrite Acfer 059) to 4562.7 ± 0.5 Ma (CB chondrite Gujba) and was either continuous or consisted of at least three discrete episodes. Since chondrules in CB chondrites appear to have formed from a vapor‐melt plume produced by a giant impact between planetary embryos after dust in the protoplanetary disk had largely dissipated (Krot et al. 2005), there were possibly a variety of processes in the early solar system occurring over at least 4–5 Myr that we now combine under the umbrella name of “chondrule formation.”     

Refractory forsterite in primitive meteorites: Condensates from the solar nebula?

Abstract— All groups of chondritic meteorites contain discrete grains of forsteritic olivine with FeO contents below 1 wt% and high concentrations of refractory elements such as Ca, Al, and Ti. Ten such grains (52 to 754 μg) with minor amounts of adhering matrix were separated from the Allende meteorite. After bulk chemical analysis by instrumental neutron activation analysis (INAA), some samples were analyzed with an electron microprobe and some with an ion microprobe. Matrix that accreted to the forsterite grains has a well‐defined unique composition, different from average Allende matrix in having higher Cr and lower Ni and Co contents, which implies limited mixing of Allende matrix. All samples have approximately chondritic relative abundances of refractory elements Ca, Al, Sc, and rare‐earth elements (REE), although some of these elements, such as Al, do not quantitatively reside in forsterite; whereas others (e.g., Ca) are intrinsic to forsterite. The chondritic refractory element ratios in bulk samples, the generally high abundance level of refractory elements, and the presence of Ca‐Al‐Ti‐rich glass inclusions suggest a genetic relationship of refractory condensates with forsteritic olivine. The Ca‐Al‐Ti‐rich glasses may have acted as nuclei for forsterite condensation. Arguments are presented that exclude an origin of refractory forsterite by crystallization from melts with compositions characteristic of Allende chondrules: (a) All forsterite grains have CaO contents between 0.5 and 0.7 wt% with no apparent zoning, requiring voluminous parental melts with 18 to 20 wt% CaO, far above the average CaO content of Allende chondrules. Similar arguments apply to Al contents. (b) The low FeO content of refractory forsterite of 0.2‐0.4 wt% imposes an upper limit of ～1 wt% of FeO on the parental melt, too low for ordinary and carbonaceous chondrule melts, (c) The Mn contents of refractory forsterites are between 30 to 40 ppm. This is at least one order of magnitude below the Mn content of chondrule olivines in all classes of meteorites. The observed Mn contents of refractory forsterite are much too low for equilibrium between olivine and melts of chondrule composition, (d) As shown earlier, refractory forsterites have O‐isotopic compositions different from chondrules (Weinbruch et al., 1993a). Refractory olivines in carbonaceous chondrites are found in matrix and in chondrules. The compositional similarity of both types was taken to indicate that all refractory forsterites formed inside chondrules (e.g., Jones, 1992). As refractory forsterite cannot have formed by crystallization from chondrule melts, we conclude that refractory forsterite from chondrules are relic grains that survived chondrule melting and probably formed in the same way as refractory forsterite enclosed in matrix. We favor an origin of refractory forsterite by condensation from an oxidized nebular gas.     

Comparison of cosmic‐ray exposure ages and trapped noble gases in chondrule and matrix samples of ordinary,enstatite, and carbonaceous chondrites

Abstract— We performed a comprehensive study of the He, Ne, and Ar isotopic abundances and of the chemical composition of bulk material and components of the H chondrites Dhajala, Bath, Cullison, Grove Mountains 98004, Nadiabondi, Ogi, and Zag, of the L chondrites Grassland, Northwest Africa 055, Pavlograd, and Ladder Creek, of the E chondrite Indarch, and of the C chondrites Hammadah al Hamra 288, Acfer 059, and Allende. We discuss a procedure and necessary assumptions for the partitioning of measured data into cosmogenic, radiogenic, implanted, and indigenous noble gas components. For stone meteorites, we derive a cosmogenic ratio ²⁰Ne/²²Ne of 0.80 ± 0.03 and a trapped solar ⁴He/³He ratio of 3310 ± 130 using our own and literature data. Chondrules and matrix from nine meteorites were analyzed. Data from Dhajala chondrules suggest that some of these may have experienced precompaction irradiation by cosmic rays. The other chondrules and matrix samples yield consistent cosmic‐ray exposure (CRE) ages within experimental errors. Some CRE ages of some of the investigated meteorites fall into clusters typically observed for the respective meteorite groups. Only Bath's CRE age falls on the 7 Ma double‐peak of H chondrites, while Ogi's fits the 22 Ma peak. The studied chondrules contain trapped ²⁰Ne and ³⁶Ar concentrations in the range of 10^?6–10^?9 cm³ STP/g. In most chondrules, trapped Ar is of type Q (ordinary chondritic Ar), which suggests that this component is indigenous to the chondrule precursor material. The history of the Cullison chondrite is special in several respects: large fractions of both CR‐produced ³He and of radiogenic ⁴He were lost during or after parent body breakup, in the latter case possibly by solar heating at small perihelion distances. Furthermore, one of the matrix samples contains constituents with a regolith history on the parent body before compaction. It also contains trapped Ne with a ²⁰Ne/²²Ne ratio of 15.5 ± 0.5, apparently fractionated solar Ne.     

Origin of fayalitic olivine rims and lath-shaped matrix olivine in the CV3 chondrite Allende and its dark inclusions

Abstract— We have studied an Allende dark inclusion by optical microscopy, scanning electron microscopy, electron microprobe analysis and transmission electron microscopy. The inclusion consists of chondrules, isolated olivines and matrix, which, as in the Allende host, is mainly composed of 5–20 μm long lath-shaped fayalitic grains with a narrow compositional range (Fa_{42 ± 2}) and nepheline. Olivine phenocrysts in chondrules and isolated olivine grains show various degrees of replacement by 5–10 μm wide fayalitic rims (Fa_{39 ± 2}) and 100–1000 μm wide translucent zones, which consist of 5–20 μm long lath-shaped fayalitic grains (Fa_{41 ± 1}) intergrown with nepheline. These fayalitic olivines, like those in the matrix of the dark inclusion, contain 10–20 nm sized inclusions of chromite, hercynite, and Fe-Ni sulfides. The fayalitic rims around remnant olivines are texturally and compositionally identical to those in Allende host, suggesting that they have similar origins. Chondrules are surrounded by opaque rims consisting of tiny lath-shaped fayalitic olivines (<1–3 μm long) intergrown with nepheline. As in the Allende host, fayalitic olivine veins may crosscut altered chondrules, fine-grained chondrule rims and extend into the matrix, indicating that alteration occurred after accretion. We infer that fayalitic olivine rims and lath-shaped fayalites in Allende and its dark inclusions formed from phyllosilicate intermediate phases. This explanation accounts for (1) the similarity of the replacement textures observed in the dark inclusion and Allende host to aqueous alteration textures in CM chondrites; (2) the anomalously high abundances of Al and Cr and the presence of tiny inclusions of spinels and sulfides in fayalitic olivines in Allende and Allende dark inclusions; (3) abundant voids and defects in lath-shaped fayalites in the Allende dark inclusion, which may be analogous to those in partly dehydrated phyllosilicates in metamorphosed CM/CI chondrites. We conclude that the matrix and chondrule rims in Allende were largely converted to phyllosilicates and then completely dehydrated. The Allende dark inclusions experienced diverse degrees of aqueous/hydrothermal alteration prior to complete dehydration. The absence of low-Ca pyroxene in the dark inclusion and its significant replacement by fayalitic olivine in Allende is consistent with the lower resistance of low-Ca pyroxene to aqueous alteration relative to forsteritic olivine. Hydro-thermal processing of Allende probably also accounts for the low abundance of planetary noble gases and interstellar grains, and the formation of nepheline, sodalite, salite-hedenbergite pyroxenes, wollastonite, kirschsteinite and andradite in chondrules and Ca,Al-rich inclusions.     

Magnesium isotopic fractionation in chondrules from the Murchison and Murray CM2 carbonaceous chondrites

We present high‐precision measurements of the Mg isotopic compositions of a suite of types I and II chondrules separated from the Murchison and Murray CM2 carbonaceous chondrites. These chondrules are olivine‐ and pyroxene‐rich and have low ²⁷Al/²⁴Mg ratios (0.012–0.316). The Mg isotopic compositions of Murray chondrules are on average lighter (δ²⁶Mg ranging from ?0.95‰ to ?0.15‰ relative to the DSM‐3 standard) than those of Murchison (δ²⁶Mg ranging from ?1.27‰ to +0.77‰). Taken together, the CM2 chondrules exhibit a narrower range of Mg isotopic compositions than those from CV and CB chondrites studied previously. The least‐altered CM2 chondrules are on average lighter (average δ²⁶Mg = ?0.39 ± 0.30‰, 2SE) than the moderately to heavily altered CM2 chondrules (average δ²⁶Mg = ?0.11 ± 0.21‰, 2SE). The compositions of CM2 chondrules are consistent with isotopic fractionation toward heavy Mg being associated with the formation of secondary silicate phases on the CM2 parent body, but were also probably affected by volatilization and recondensation processes involved in their original formation. The low‐Al CM2 chondrules analyzed here do not exhibit any mass‐independent variations in ²⁶Mg from the decay of ²⁶Al, with the exception of two chondrules that show only small variations just outside of the analytical error. In the case of the chondrule with the highest Al/Mg ratio (a type IAB chondrule from Murchison), the lack of resolvable ²⁶Mg excess suggests that it either formed >1 Ma after calcium‐aluminum‐rich inclusions, or that its Al‐Mg isotope systematics were reset by secondary alteration processes on the CM2 chondrite parent body after the decay of ²⁶Al.     

Extraterrestrial amino acids and L‐enantiomeric excesses in the CM2 carbonaceous chondrites Aguas Zarcas and Murchison

The abundances, distributions, enantiomeric ratios, and carbon isotopic compositions of amino acids in two fragments of the Aguas Zarcas CM2 type carbonaceous chondrite fall and a fragment of the CM2 Murchison meteorite were determined via liquid chromatography time‐of‐flight mass spectrometry and gas chromatography isotope ratio mass spectrometry. A suite of two‐ to six‐carbon aliphatic primary amino acids was identified in the Aguas Zarcas and Murchison meteorites with abundances ranging from ~0.1 to 158 nmol/g. The high relative abundances of α‐amino acids found in these meteorites are consistent with a Strecker‐cyanohydrin synthesis on these meteorite parent bodies. Amino acid enantiomeric and carbon isotopic measurements in both fragments of the Aguas Zarcas meteorites indicate that both samples experienced some terrestrial protein amino acid contamination after their fall to Earth. In contrast, similar measurements of alanine in Murchison revealed that this common protein amino acid was both racemic (D ≈ L) and heavily enriched in ¹³C, indicating no measurable terrestrial alanine contamination of this meteorite. Carbon isotope measurements of two rare non‐proteinogenic amino acids in the Aguas Zarcas and Murchison meteorites, α‐aminoisobutyric acid and D‐ and L‐isovaline, also fall well outside the typical terrestrial range, confirming they are extraterrestrial in origin. The detections of non‐terrestrial L‐isovaline excesses of ~10–15% in both the Aguas Zarcas and Murchison meteorites, and non‐terrestrial L‐glutamic acid excesses in Murchison of ~16–40% are consistent with preferential enrichment of circularly polarized light generated L‐amino acid excesses of conglomerate enantiopure crystals during parent body aqueous alteration and provide evidence of an early solar system formation bias toward L‐amino acids prior to the origin of life.     

Petrographic comparison of refractory inclusions from different chemical groups of chondrites

Abstract— Twenty‐four refractory inclusions (40–230 μm, with average of 86 ± 40 μm) were found by X‐ray mapping of 18 ordinary chondrites. All inclusions are heavily altered, consisting of finegrained feldspathoids, spinel, and Ca‐pyroxene with minor ilmenite. The presence of feldspathoids and lack of melilite are due to alteration that took place under oxidizing conditions as indicated by FeO‐ZnO‐rich spinel and ilmenite. The pre‐altered mineral assemblages are dominated by two types: one rich in melilite, referred to as type A‐like, and the other rich in spinel, referred to as spinelpyroxene inclusions. This study and previous data show similar type and size distributions of refractory inclusions in ordinary and enstatite chondrites. A survey of refractory inclusions was also conducted on Allende and Murchison in order to make unbiased comparison with their counterparts in other chondrites. The predominant inclusions are type A and spinel‐pyroxene, with average sizes of 170 ± 130 μm (except for two mm‐sized inclusions) in Allende and 150 ± 100 μm in Murchison. The relatively larger sizes are partially due to common conglomerating of smaller nodules in both chondrites. The survey reveals closely similar type and size distributions of refractory inclusions in various chondrites, consistent with our previous data of other carbonaceous chondrites. The petrographic observations suggest that refractory inclusions in various groups of chondrites had primarily formed under similar processes and conditions, and were transported to different chondrite‐accreting regions. Heterogeneous abundance and distinct alteration assemblages of refractory inclusions from various chondrites could be contributed to transporting processes and secondary reactions under different conditions.     

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.     

Carbon in glass inclusions in the Allende meteorite

Abstract— Olivines in chondrules of the Allende CV3 carbonaceous chondrite contain two types of micron sized silicate melt inclusions: clear glass (type I) and devitrified glass (type II) inclusions. Many of the type I inclusions contain a gas bubble of variable size. Type II inclusions can be transparent (IIa), with or without a gas bubble, and brown (type IIb), with a gas bubble. A number of inclusions were measured with the Raman microprobe to detect possible presence of carbon. Carbon in the form of graphite was detected only in type II inclusions. Compositions of 11 inclusions were determined with the electron microprobe and proton microprobe in search for possible explanation of this preference of carbon for devitrified inclusions. All of the measured inclusions are rich in Si, Al and Ca. No significant differences between the compositions of the two types of inclusions were found. The data suggest that the inclusions formed from the melt trapped in growing olivine crystals, which themselves crystallized from a silicon rich, gas bearing melt. There is no coherent relation between the occurrence of graphite and the gas abundance in the original melt, as indicated by the sizes of gas bubbles. Therefore, carbon was not combined in a gaseous species (e.g., CO). It must have been preferentially dissolved in some domains of the melt.     

The Ningqiang Meteorite: Classification and Petrology of an Anomalous CV Chondrite

Abstract— Ningqiang is an anomalous CV chondrite (oxidized subgroup) containing a high abundance of aggregational inclusions (13.7 vol.%) and low abundances of refractory inclusions (1.0^+1.0_–0.5 vol.%) and bulk refractory lithophiles (～0.82 × CV). Ningqiang may have agglomerated after most refractory inclusions at the nebular midplane had already been incorporated into other objects. Coarse-grained rims surround only ～5% of Ningqiang chondrules, compared to ～50% in normal CV chondrites. Aggregational inclusions appear to have formed by incipient melting of fine-grained aggregates at relatively low temperatures in the solar nebula, possibly by the mechanism responsible for chondrule formation. Granoblastic porphyritic chondrules, which contain olivines forming 120° triple junctures and no mesostasis, probably formed in the solar nebula by incomplete melting of precursor materials that were olivine normative and had relatively low concentrations of Si, Ca, Al, Fe and Na.     

Rare-earth elements in matrix,inclusions, and chondrules of the Allende meteorite

Rare-earth elements in a whole-rock sample and in major components of the Allende meteorite were investigated; for a few samples, abundances of Ba, Sr, Ca, and Al were also determined. Of the materials investigated in the present work, CaAl-rich inclusions G and O seem to be of the greatest significance. In spite of the minor difference in mineralogy between them, the apparent chondrite-normalized RE pattern is much different between these two inclusions. (Yb and Eu in inclusion G appear exceptionally irregular). This observation is inferred to reflect a rather subtle difference in condition of condensation. It is also worthwhile to note that, while two portions (pink and white) of the inclusion G show similar aspects in the abundances of lithophile trace elements investigated, they show a remarkable difference at the same time. The white portion (G_w) of inclusion G can be considered to be a mixture of chondritic material and highly fractionated material like the faintly pink portion (G_p) picked from the same inclusion. This would suggest the possibility that the G_p-like material was produced from chondritic dust.The “matrix” separated from Allende was found to be fractionated with respect to the RE abundances relative to representative chondrite. It has also a very high value for the Ba abundance.     

A petrographic,chemical, and isotopic study of calcium‐aluminum‐rich inclusions and aluminum‐rich chondrules from the Axtell (CV3) chondrite

Abstract— Petrographic, compositional, and isotopic characteristics were studied for three calcium‐aluminum‐rich inclusions (CAIs) and four plagioclase‐bearing chondrules (three of them Al‐rich) from the Axtell (CV3) chondrite. All seven objects have analogues in Allende (CV3) and other primitive chondrites, yet Axtell, like most other chondrites, contains a distinctive suite of CAIs and chondrules. In common with Allende CAIs, CAIs in Axtell exhibit initial ²⁶Al/²⁷Al ratios ((²⁶Al/²⁷Al)₀) ranging from ～5 × 10^?5 to <1.1 × 10^?5, and plagioclase‐bearing chondrules have (²⁶Al/²⁷Al)₀ ratios of ～3 × 10^?6 and lower. One type‐A CAI has the characteristics of a FUN inclusion. The Al‐Mg data imply that the plagioclase‐bearing chondrules began to form >2 Ma after the first CAIs. As in other CV3 chondrites, some objects in Axtell show evidence of isotopic disturbance. Axtell has experienced only mild thermal metamorphism (<600 °C), probably not enough to disturb the Al‐Mg systematics. Its CAIs and chondrules have suffered extensive metasomatism, probably prior to final accretion. These data indicate that CAIs and chondrules in Axtell (and other meteorites) had an extended history of several million years before their incorporation into the Axtell parent body. These long time periods appear to require a mechanism in the early solar system to prevent CAIs and chondrules from falling into the Sun via gas drag for several million years before final accretion. We also examined the compositional relationships among the four plagioclase‐bearing chondrules (two with large anorthite laths and two barred‐olivine chondrules) and between the chondrules and CAIs. Three processes were examined: (1) igneous differentiation, (2) assimilation of a CAI by average nebular material, and (3) evaporation of volatile elements from average nebular material. We find no evidence that igneous differentiation played a role in producing the chondrule compositions, although the barred olivine compositions can be related by addition or subtraction of olivine. Methods (2) and (3) could have produced the composition of one chondrule, AXCH‐1471, but neither process explains the other compositions. Our study indicates that plagioclase‐bearing objects originated through a variety of processes.     

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.     

REE abundances in the matrix of the Allende (CV) meteorite: Implications for matrix origin

Abstract— The trace element distributions in the matrix of primitive chondrites were examined using four least‐contaminated matrix specimens from the polished sections of the Allende (CV) meteorite. Analysis of rare earth element (REE), Ba, Sr, Rb, and K abundances by isotope dilution mass spectrometry revealed that the elemental abundances of lithophile elements except for alkali metals (K, Rb) in the specimens of the Allende matrix studied here are nearly CI (carbonaceous Orgueil) chondritic (～1 × CI). Compared to refractory elements, all the matrix samples exhibited systematic depletion of the moderately volatile elements K and Rb (0.1–0.5 × CI). We suggest that the matrix precursor material did not carry significant amounts of alkali metals or that the alkalis were removed from the matrix precursor material during the parent body process and/or before matrix formation and accretion. The matrix specimens displayed slightly fractionated REE abundance patterns with positive Ce anomalies (CI‐normalized La/Yb ratio = 1.32–1.65; Ce/Ce* = 1.16–1.28; Eu/Eu* = 0.98–1.10). The REE features of the Allende matrix do not indicate a direct relationship with chondrules or calcium‐aluminum‐rich inclusions (CAIs), which in turn suggests that the matrix was not formed from materials produced by the breakage and disaggregation of the chondrules or CAIs. Therefore, we infer that the Allende matrix retains the REE features acquired during the condensation process in the nebula gas.     

Fabric analysis of Allende matrix using EBSD

Abstract— Fabric analysis of the interstitial matrix material in primitive meteorites offers a novel window on asteroid formation and evolution. Electron backscatter diffraction (EBSD) has allowed fabrics in these fine‐grained materials to be visualized in detail for the first time. Our data reveal that Allende, a CV3 chondrite, possesses a uniform, planar, short‐axis alignment fabric that is pervasive on a broad scale and is probably the result of deformational shortening related to impact or gravitational compaction. Interference between this matrix fabric and the larger, more rigid components, such as dark inclusions (DIs) and calcium‐aluminium‐rich inclusions (CAIs), has lead to the development of locally oriented and intensified matrix fabrics. In addition, DIs possess fabrics that are conformable with the broader matrix fabric. These results suggest that DIs were in situ prior to the deformational shortening event responsible for these fabrics, thus providing an argument against dark inclusions being fragments from another lithified part of the asteroid (Kojima and Tomeoka 1996; Fruland et al. 1978). Moreover, both DIs and Allende matrix are highly porous (?25%) (Corrigan et al. 1997). Mobilizing a highly porous DI during impact‐induced brecciation without imposing a fabric and incorporating it into a highly porous matrix without significantly compacting these materials is improbable. We favor a model that involves Allende DIs, CAIs, and matrix accreting together and experiencing the same deformation events.