Chemical and physical studies of type 3 chondrites—V: The enstatite chondrites

We report instrumental neutron activation analysis determinations of 19 major, minor and trace elements in three enstatite chondrites. Based on these, and literature data on the bulk and mineral composition of enstatite chondrites, we discuss the history of the type 3 or unequilibrated enstatite chondrites, and their relationship with the other enstatite chondrites. The type 3 enstatite chondrites have E chondrite lithophile element abundances and their siderophile element abundances place them with the EH chondrites, well resolved from the EL chondrites. Moderately volatile chalcophile elements are at the low end of the EH range and Cr appears to be intermediate between EH and EL. We suggest that the type 3 enstatite chondrites are EH chondrites which have suffered small depletions of certain chalcophile elements through the loss of shock-produced sulfurous liquids. The oxygen isotope differences between type 3 and other enstatite chondrites is consistent with equilibration with the nebula gas ~30° higher than the others, or with the loss of a plagioclase-rich liquid. The mineral chemistry of the type 3 chondrites is consistent with either low temperature equilibration, or, in some instances, with shock effects.     

陨石中前太阳颗粒及其所携带惰性气体的原始同位素异常研究进展

从球粒陨石的酸不溶残渣中分离出了携带有惰性气体同位素异常的金刚石、碳化硅和石墨颗粒。这些同位素异常用太阳系内部过程是无法解释的，它们被归因于太阳系外多种核合成组分的不完全混合，称为原始惰性气体同位素异常，这三种矿物颗粒被称为前太阳颗粒。介绍了这三种前太阳颗粒的分离过程、存在部位、粒度大小、所携带惰性气体组分的同位素组成，以及这些惰性气体和携带物的成因，并对它们的科学意义进行了简要的讨论。     

Refractory trace elements in Ca-Al-rich inclusions in the Allende meteorite

The condensation temperatures are calculated for a number of refractory trace metals from a gas of solar composition at 10^?3 and 10^?4 atm. total pressure. Instrumental neutron activation analysis of Ca-Al-rich inclusions in the Allende carbonaceous chondrite reveals enrichments of 22.8 ± 2.2 in the concentrations of Ir, Sc and the rare earths relative to Cl chondrites. Such enrichments cannot be due to magmatic differentiation processes because of the marked differences in chemical behavior between Ir and Sc, exhibited by their distributions in terrestrial igneous rocks and meteorites. All of these elements should have condensed from a cooling gas of solar composition above or within the range of condensation temperatures of the major mineral phases of the inclusions, which suggests that these inclusions are high-temperature condensates from the primitive solar nebula. Gas-dust fractionation of these materials may have been responsible for the depletion of refractory elements in the ordinary and enstatite chondrites relative to the carbonaceous chondrites.     

Nature of the carbon and sulfur phases and inorganic gases in the Kenna ureilite

Abundances of carbon and sulfur in the Kenna ureilite are 2.219 ± 0.060 wt. % C and 0.179 ± 0.008 wt. % S. Secondary carbonates resulting from terrestrial weathering account for 0.25 ± 0.02 wt. % C. No hydrocarbons were detected during gas release measurements. Most of the carbon is in graphite, diamond, or lonsdaleite. The sample of Kenna contained 0.95 ± 0.05 wt. % H₂O. Total carbon and sulfur measurements were made on three additional ureilites: Haverö, Dingo Pup Donga, and North Haig. Ureilite carbon abundances are similar to those of C-2 chondrites, whereas sulfur abundances are a factor of 10 less than C-2 chondrites and ordinary chondrites. The elemental abundances, ratios, and phases present in the ureilites rule out a direct genetic relationship between the ureilites and the carbonaceous chondrites.     

Condensation in the primitive solar nebula

The distribution of the major elements between vapor and solid has been calculated for a cooling gas of cosmic composition. The assumption is made that high temperature condensates remain in equilibrium with the vapor, affecting the temperatures of appearance of successively less refractory phases. The model suggests that the major textural features and mineralogical composition of the Ca, Al-rich inclusions in the C3 chondrites were produced during condensation in the nebula characterized by slight departures from chemical equilibrium due to incomplete reaction of high temperature condensates. Fractionation of such a phase assemblage is sufficient to produce part of the lithophile element depletion of the ordinary chondrites relative to the cosmic abundances.     

A reappraisal of the metamorphic history of EH3 and EL3 enstatite chondrites

The thermal history of a series of EH3 and EL3 chondrites has been investigated by studying the degree of structural order of the organic matter (OM) located and characterized in matrix areas by Raman micro-spectroscopy. By comparison with unequilibrated ordinary chondrites (UOCs) and CO and CV carbonaceous chondrites, the following petrologic types have been assigned to various E chondrites: Sahara 97096 and Allan Hills 84206: 3.1-3.4; Allan Hills 85170 and Parsa: 3.5; Allan Hills 85119: 3.7; Qingzhen, MacAlpine Hills 88136 and MacAlpine Hills 88184: 3.6-3.7. The petrologic type of Qingzhen is consistent with the abundance of the P3 noble gas component, a sensitive tracer of the grade of thermal metamorphism. The petrologic types are qualitatively consistent with the abundance of fine-grained matrix for the whole series. No significant effects of shock processes on the structure of OM were observed. However such processes certainly compete with thermal metamorphism and the possibility of an effect cannot be fully discarded, in particular in the less metamorphosed objects. The OM precursors accreted by the EH3 and EL3 parent bodies appear to be fairly similar to those of UOCs and CO and CV carbonaceous chondrites. Raman data however show some slight structural differences that could be partly accounted for by shock processes. The metamorphic history of EH3 and EL3 chondrites has often been described as complex, in particular regarding the combined action of shock and thermal metamorphism. Because OM maturity is mostly controlled by the temperature of peak metamorphism, it is possible to distinguish between the contributions of long duration thermal processes and that of shock processes. Comparison of the petrologic types with the closure temperatures previously derived from opaque mineral assemblages has revealed that the thermal history of EH3 and EL3 chondrites is consistent with a simple asteroidal onion shell model. Thermal metamorphism in enstatite chondrites appears to be fairly similar to that which takes place in other chondrite classes. The complex features recorded by mineralogy and petrology and widely reported in the literature appear to be mostly controlled by shock processes.     

The Rumuruti chondrite group

Since 1994, the Rumuruti (R) chondrites have been recognized as a new, well-established chondrite group differing from carbonaceous, ordinary, and enstatite chondrites. The first R chondrite, Carlisle Lakes, was found in Australia in 1977. Meanwhile, the number has increased to 107 (December, 2010). This group is named after the Rumuruti meteorite, the first and so far the only R chondrite fall. Most of the R chondrites are breccias containing a variety of different clasts embedded in a clastic matrix. Some textural and mineralogical characteristics can be summarized as follows: (a) the chondrule abundance in large fragments and in unbrecciated rocks is ∼35–50 vol%; (b) Ca,Al-rich inclusions are rare; (c) the olivine abundance is typically 65–78 vol%; (d) the mean chondrule diameter is ∼400 μm; (e) in unequilibrated R chondrites, low-Ca pyroxene is dominating, whereas in equilibrated R chondrites it is Ca-rich pyroxene; (f) the typical olivine in a metamorphosed lithology is ∼Fa_38–40; (g) matrix olivine in unequilibrated, type 3 fragments and rocks has much higher Fa (∼45–60 mol%) compared to matrix olivines in type 4–6 lithologies (∼Fa_38–41); (h) spinels have a high TiO₂ of ∼5 wt%; (i) abundant different noble metal-bearing phases (metals, sulfides, tellurides, arsenides) occur. The exception is the metamorphosed, type 5/6 R chondrite La Paz Icefield 04840 which contains hornblende, phlogopite, and Ca-poor pyroxene, the latter phase typically occurring in low-grade metamorphosed R chondrites only.In bulk composition, R chondrites have some affinity to ordinary chondrites: (a) the absence of significant depletions in Mn and Na in R chondrites and ordinary chondrites is an important feature to distinguish these groups from carbonaceous chondrites; (b) total Fe (∼24 wt%) of R chondrites is between those of H and L chondrites (27.1 and 21.6 wt%, respectively); (c) the average CI/Mg-normalized lithophile element abundances are ∼0.95 × CI, which is lower than those for carbonaceous chondrites (≥1.0 × CI) and slightly higher than those for ordinary chondrites (∼0.9 × CI); (d) trace element concentrations such as Zn (∼150 ppm) and Se (∼15 ppm) are much higher than in ordinary chondrites; (e) the whole rock Δ¹⁷O of ∼2.7 for R chondrites is the highest among all meteorite groups, and the mean oxygen isotope composition is δ¹⁷O = 5.36 ± 0.43, δ¹⁸O = 5.07 ± 0.86, Δ¹⁷O = +2.72 ± 0.31; (f) noble gas cosmic ray exposure ages of R chondrites range between ∼0.1 and ∼70 Ma. More than half of the R chondrites analyzed for noble gases contain implanted solar wind and, thus, are regolith breccias. The 43 R chondrites from Northern Africa analyzed so far for noble gases seem to represent at least 16 falls. Although the data base is still scarce, the data hint at a major collision event on the R chondrite parent body between 15 and 25 Ma ago.     

Formation of metal in the CH chondrites ALH 85085 and PCA 91467

Siderophile element distributions within individual metal grains in two CH chondrites, Allan Hills 85085 and Pecora Escarpment 91467, were measured by laser ablation inductively coupled plasma mass spectrometry. Those metal grains that are zoned in Ni were also found to be zoned in other refractory siderophile elements, such as Ru, but not in Pd, which is not refractory but is highly siderophile. This pattern is consistent with an origin by condensation from a gas of approximately solar composition, but not with an origin by redox processes or fractional crystallization. The unzoned metal grains in CH chondrites were found to be frequently depleted in Ru but not in Pd, consistent with later stage condensation from a solar gas after removal of the zoned metal. Gold is inversely correlated with Ni in the unzoned metal grains, and mean Au abundances in zoned metal are always low. Both zoned and unzoned metal in CH chondrites could plausibly be produced from a thermostatically regulated nebula, followed by rapid removal of the zoned metal, and slower removal of the unzoned metal, both at temperatures near or above the condensation temperature of Au (∼1250 K). This is also consistent with the isolation temperatures inferred from silicate grains in CH chondrites by previous workers based on their volatile element inventories. The volatile siderophile Cu is enriched in the rims relative to the interiors of both zoned and unzoned grains, and is interpreted as the product of diffusion during low-grade thermal processing. The similarity of Cu distributions, and degree of kamacite/taenite exsolution, between zoned and unzoned metal in CH chondrites suggests that the two populations of metal experienced modest thermal metamorphism after they were brought together in the same environment, probably on the CH parent body. Fragmentation and size-sorting of the metal must have post-dated the Cu zoning, and may have occurred in a regolith on the CH parent body. The compositions of CH metal, like that of metal from QUE 94411 and HH 237, are consistent with a nebular origin, and may be the most primitive nebular materials (as distinct from presolar grains) sampled by chondrites.     

26AI in stony meteorites with gas losses

²⁶Al contents of 16 meteorites with ³He losses have the same average values as all chondrites indicating that gas losses did not occur in a recent, prolonged exposure to unusual cosmic-ray activity.     

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.     

陨石原始型惰性气体的研究进展——Q气及其携带物特征

陨石中的原始型惰性气体是在陨石形成前或陨石形成期间,组成陨石的物质通过吸附、溶解等方式将原始太阳星云中的惰性气体保留在陨石中形成的。实验研究发现,球粒陨石中的原始型惰性气体浓集中一种称为Q相的物质中,因此在原始型惰性气体中占绝对优势的组分被称为Q气或P1气。介绍了陨石原型惰性气体概念的由来、Q相的发现经过、Q相的成分和在球粒陨石中的存在部位以及Q气的元素丰度和同位素组成。并根据不同类型损石中Q气的分配情况,对其成因意义进行了讨论。     

Amoeboid olivine aggregates and related objects in carbonaceous chondrites: records of nebular and asteroid processes

Amoeboid olivine aggregates (AOAs) are the most common type of refractory inclusions in CM, CR, CH, CV, CO, and ungrouped carbonaceous chondrites Acfer 094 and Adelaide; only one AOA was found in the CB_b chondrite Hammadah al Hamra 237 and none were observed in the CB_a chondrites Bencubbin, Gujba, and Weatherford. In primitive (unaltered and unmetamorphosed) carbonaceous chondrites, AOAs consist of forsterite (Fa_<2), Fe, Ni-metal (5-12 wt% Ni), and Ca, Al-rich inclusions (CAIs) composed of Al-diopside, spinel, anorthite, and very rare melilite. Melilite is typically replaced by a fine-grained mixture of spinel, Al-diopside, and ±anorthite; spinel is replaced by anorthite. About 10% of AOAs contain low-Ca pyroxene replacing forsterite. Forsterite and spinel are always ¹⁶O-rich (δ^17,18O∼−40‰ to −50‰), whereas melilite, anorthite, and diopside could be either similarly ¹⁶O-rich or ¹⁶O-depleted to varying degrees; the latter is common in AOAs from altered and metamorphosed carbonaceous chondrites such as some CVs and COs. Low-Ca pyroxene is either ¹⁶O-rich (δ^17,18O∼−40‰) or ¹⁶O-poor (δ^17,18O∼0‰). Most AOAs in CV chondrites have unfractionated (∼2-10×CI) rare-earth element patterns. AOAs have similar textures, mineralogy and oxygen isotopic compositions to those of forsterite-rich accretionary rims surrounding different types of CAIs (compact and fluffy Type A, Type B, and fine-grained, spinel-rich) in CV and CR chondrites. AOAs in primitive carbonaceous chondrites show no evidence for alteration and thermal metamorphism. Secondary minerals in AOAs from CR, CM, and CO, and CV chondrites are similar to those in chondrules, CAIs, and matrices of their host meteorites and include phyllosilicates, magnetite, carbonates, nepheline, sodalite, grossular, wollastonite, hedenbergite, andradite, and ferrous olivine.Our observations and a thermodynamic analysis suggest that AOAs and forsterite-rich accretionary rims formed in ¹⁶O-rich gaseous reservoirs, probably in the CAI-forming region(s), as aggregates of solar nebular condensates originally composed of forsterite, Fe, Ni-metal, and CAIs. Some of the CAIs were melted prior to aggregation into AOAs and experienced formation of Wark-Lovering rims. Before and possibly after the aggregation, melilite and spinel in CAIs reacted with SiO and Mg of the solar nebula gas enriched in ¹⁶O to form Al-diopside and anorthite. Forsterite in some AOAs reacted with ¹⁶O-enriched SiO gas to form low-Ca pyroxene. Some other AOAs were either reheated in ¹⁶O-poor gaseous reservoirs or coated by ¹⁶O-depleted pyroxene-rich dust and melted to varying degrees, possibly during chondrule formation. The most extensively melted AOAs experienced oxygen isotope exchange with ¹⁶O-poor nebular gas and may have been transformed into magnesian (Type I) chondrules. Secondary mineralization and at least some of the oxygen isotope exchange in AOAs from altered and metamorphosed chondrites must have resulted from alteration in the presence of aqueous solutions after aggregation and lithification of the chondrite parent asteroids.     

Matrices of type 3 ordinary chondrites—primitive nebular records

Petrologic studies were made on the fine-grained matrices of type 3 ordinary chondrites of the lowest petrologic subtype. The matrix minerals, in order of abundance, are olivine (Fo₉₉ to Fo₉), enstatite or bronzite, augite or subcalcic augite, albite, Fe-Ni metal, troilite, magnetite, spinel (MgAl₂O₄), chromite, and calcite. Fe- and Mg-rich fluffy particles and albite-like particles are also major constituents. The chemical compositions of olivine and pyroxenes vary within and among the chondrites and are in gross disequilibrium, showing that the matrix materials were hardly heated after their formation. Textural relationships indicate that magnesian olivine was formed after Ca-pyroxene, followed by intermediate to iron-rich olivine. Intermediate olivine was formed from enstatite and metallic iron under relatively oxidizing conditions. The observations indicate that matrices of chondrites are neither the fragments of chondrules nor the precursors of chondrules. They were mostly the products of condensation and reaction among solids and/or between solids and the ambient gas mostly at low temperatures, and thus they contain records of primitive processes in the nebula. In order to explain the presence of olivines more iron-rich than Fo₅₀, the presence of free SiO₂ or a high activity of SiO₂ in the gas is necessary, which was not shown in previous thermochemical calculations. Mineral assemblages of matrix minerals of chondrites of different chemical groups differ systematically according to oxidation state of the parental meteorites, indicating that they were formed at different oxygen fugacities. The rims of chondrules, and surrounding matrix materials, must have accreted onto chondrules during turbulent movements of the nebula.     

Chemical and physical studies of type 3 chondrites—VI: Siderophile elements in ordinary chondrites

The abundances of Fe, Ni, Co, Au, Ir, Ga, As and Mg have been determined by instrumental neutron activation analysis in 38 type 3 ordinary chondrites (10 of which may be paired) and 15 equilibrated chondrites. Classification of type 3 ordinary chondrites into the H, L and LL classes using oxygen isotopes and parameters which reflect oxidation state (Fa and Fs in the olivine and pyroxene and Co in kamacite) is difficult or impossible. Bulk compositional parameters, based on the equilibrated chondrites, have therefore been used to classify the type 3 chondrites. The distribution of the type 3 ordinary chondrites over the classes is very different from that of the equilibrated chondrites, the LL chondrites being more heavily represented. The type 3 ordinary chondrites contain 5 to 15 percent lower abundances of siderophile elements and a compilation of the present data and literature data indicates a small, systematic decrease in siderophile element concentration with decreasing petrologic type. The type 3 ordinary chondrites have, like the equilibrated ordinary chondrites, suffered a fractionation of their siderophile elements, but the loss of Ni in comparison with Au and Ir is greater for the type 3 chondrites. These siderophile element trends were established at the nebula phase of chondritic history and the co-variation with petrologic type implies onion-shell structures for the ordinary chondrite parent bodies. It is also clear that the relationship between the type 3 and the equilibrated ordinary chondrites involves more than simple, closed-system metamorphism.     

根据40Ar/39Ar年龄谱探讨陨石冲击事件的分期

⁴⁰Ar/³⁹Ar年龄谱是研究陨石冲击事件的重要资料。根据对55块陨石⁴⁰Ar/³⁹Ar冲击年龄和陨石暴露年龄的分析,发现陨石的冲击年龄与陨石类型之间存在对应关系。据此,将陨石冲击事件划分为九期。其中3900-4000Ma、470-540Ma和小于65Ma是陨石母体的三个重要演化阶段。阶段Ⅰ、Ⅱ和Ⅲ(冲击年龄大于30亿年)主要涉及高钙型无球粒陨石。所有球粒陨石的冲击年龄均小于30亿年。陨石暴露年龄因类型而异,铁陨石最大,石铁陨石次之,石陨石最小。     

Coarse-grained chondrule rims in type 3 chondrites

Relatively coarse-grained rims occur around all types of chondrules in type 3 carbonaceous and ordinary chondrites. Those in H-L-LL3 chondrites are composed primarily of olivine and low-Ca pyroxene; those in CV3 chondrites contain much less low-Ca pyroxene. Average grain sizes range from ～4 μm in H-L-LL3 chondrites to ～10 μm in CV3 chondrites. Such rims surround ～50%, ～10% and ≤ 1% of chondrules in CV3, H-L-LL3 and CO3 chondrites, respectively, but are rare (≤1%) around CV3 Ca,Al-rich inclusions. Rim thicknesses average ～150 μm in H-L-LL3 chondrites and ～400 μm in CV3 chondrites.The rims in H-L-LL3 chondrites are composed of material very similar to that which comprises darkzoned chondrules and recrysiallized matrix. Dark-zoned chondrules and coarse-grained rims probably formed in the solar nebula from clumps of opaque matrix material heated to sub-solidus to sub-liquidus temperatures during chondrule formation. Mechanisms capable of completely melting some material while only sintering other material require steep thermal gradients; suitable processes are lightning, reconnecting magnetic field lines and, possibly, aerodynamic drag heating.CV chondrites may have formed in a region where the chondrule formation mechanism was less efficient, probably at greater solar distances than the ordinary chondrites. The lesser efficiency of heating could be responsible for the greater abundance of coarse-grained rims around CV chondrules. Alternatively, CV chondrules may have suffered fewer particle collisions prior to agglomeration.     

Can the ordinary chondrites have condensed from a gas phase?

The conditions under which ordinary chondrites containing iron in three different chemical states can form in thermodynamic equilibrium with a gas phase are calculated. Hydrogen depletion factors of 10²–10³ are obtained and the formation of liquid condensates from residual gases occurs at pressures (prior to hydrogen depletion) of ?1 atm.     

Compositions of three low-FeO ordinary chondrites: Indications of a common origin with the H chondrites

Burnwell, EET 96031, and LAP 04575 are ordinary chondrites (OC) that possess lower than typical olivine Fa content than has been established for the H chondrites (<∼17 mol%). Mean low-Ca pyroxene Fs contents are typically lower than mean Fa content, with generally ?16 mol% Fs. We have investigated these three low-FeO chondrites by measuring their trace element abundances, oxygen isotopic compositions, and examining their three-dimensional (3D) petrography with synchrotron X-ray microtomography. We compare our results with those established for more common OC. The low FeO chondrites studied here have bulk trace element abundances that are identical to the H chondrites. From bulk oxygen isotopic analysis, we show that Burnwell, EET 96010, and LAP 04757 sampled oxygen reservoirs identical to the H chondrites. Burnwell, EET 96031, and LAP 04575 possess common 3D opaque mineral structures that could be distinct from the H chondrites, as evidenced by X-ray microtomographic analysis, but our comparison suite of H chondrites is small and unrepresentative. Overall, our data suggest a common origin for the low-FeO chondrites Burnwell, EET 96010, and LAP 04757 and the H chondrites. These three samples are simply extreme members of a redox process where a limiting nebular oxidizing agent, probably ice, reacted with material containing slightly higher amounts of metal than typically seen in the H chondrites.