Olivine dissolution in molten silicates: An experimental study with application to chondrule formation

Mg‐rich olivine is a ubiquitous phase in type I porphyritic chondrules in various classes of chondritic meteorites. The anhedral shape of olivine grains, their size distribution, as well as their poikilitic textures within low‐Ca pyroxene suggest that olivines suffer dissolution during chondrule formation. Owing to a set of high‐temperature experiments (1450–1540 °C) we determined the kinetics of resorption of forsterite in molten silicates, using for the first time X‐ray microtomography. Results indicate that forsterite dissolution in chondrule‐like melts is a very fast process with rates that range from ~5 μm min^?1 to ~22 μm min^?1. Forsterite dissolution strongly depends on the melt composition, with rates decreasing with increasing the magnesium and/or the silica content of the melt. An empirical model based on forsterite saturation and viscosity of the starting melt composition successfully reproduces the forsteritic olivine dissolution rates as a function of temperature and composition for both our experiments and those of the literature. Application of our results to chondrules could explain the textures of zoned type I chondrules during their formation by gas‐melt interaction. We show that the olivine/liquid ratio on one hand and the silica entrance from the gas phase (SiO_g) into the chondrule melt on the other hand, have counteracting effects on the Mg‐rich olivine dissolution behavior. Silica entrance would favor dissolution by maintaining disequilibrium between olivine and melt. Hence, this would explain the preferential dissolution of olivine as well as the preferential abundances of pyroxene at the margins of chondrules. Incipient dissolution would also occur in the silica‐poorer melt of chondrule core but should be followed by crystallization of new olivine (overgrowth and/or newly grown crystals). While explaining textures and grain size distributions of olivines, as well as the centripetal distribution of low‐Ca pyroxene in porphyritic chondrules, this scenario could also be consistent with the diverse chemical, isotopic, and thermal conditions recorded by olivines in a given chondrule.     

Silica‐rich igneous rims around magnesian chondrules in CR carbonaceous chondrites: Evidence for condensation origin from fractionated nebular gas

Abstract— The outer portions of many type I chondrules (Fa and Fs <5 mol%) in CR chondrites (except Renazzo and Al Rais) consist of silica‐rich igneous rims (SIRs). The host chondrules are often layered and have a porphyritic core surrounded by a coarse‐grained igneous rim rich in low‐Ca pyroxene. The SIRs are sulfide‐free and consist of igneously‐zoned low‐Ca and high‐Ca pyroxenes, glassy mesostasis, Fe, Ni‐metal nodules, and a nearly pure SiO₂ phase. The high‐Ca pyroxenes in these rims are enriched in Cr (up to 3.5 wt% Cr₂O₃) and Mn (up to 4.4 wt% MnO) and depleted in Al and Ti relative to those in the host chondrules, and contain detectable Na (up to 0.2 wt% Na₂O). Mesostases show systematic compositional variations: Si, Na, K, and Mn contents increase, whereas Ca, Mg, Al, and Cr contents decrease from chondrule core, through pyroxene‐rich igneous rim (PIR), and to SIR; FeO content remains nearly constant. Glass melt inclusions in olivine phenocrysts in the chondrule cores have high Ca and Al, and low Si, with Na, K, and Mn contents that are below electron microprobe detection limits. Fe, Ni‐metal grains in SIRs are depleted in Ni and Co relative to those in the host chondrules. The presence of sulfide‐free, SIRs around sulfide‐free type I chondrules in CR chondrites may indicate that these chondrules formed at high (>800 K) ambient nebular temperatures and escaped remelting at lower ambient temperatures. We suggest that these rims formed either by gas‐solid condensation of silica‐normative materials onto chondrule surfaces and subsequent incomplete melting, or by direct SiO_(gas) condensation into chondrule melts. In either case, the condensation occurred from a fractionated, nebular gas enriched in Si, Na, K, Mn, and Cr relative to Mg. The fractionation of these lithophile elements could be due to isolation (in the chondrules) of the higher temperature condensates from reaction with the nebular gas or to evaporation‐recondensation of these elements during chondrule formation. These mechanisms and the observed increase in pyroxene/olivine ratio toward the peripheries of most type I chondrules in CR, CV, and ordinary chondrites may explain the origin of olivine‐rich and pyroxene‐rich chondrules in general.     

The formation and alteration of the Renazzo‐like carbonaceous chondrites III: Toward understanding the genesis of ferromagnesian chondrules

To better understand the formation conditions of ferromagnesian chondrules from the Renazzo‐like carbonaceous (CR) chondrites, a systematic study of 210 chondrules from 15 CR chondrites was conducted. The texture and composition of silicate and opaque minerals from each observed FeO‐rich (type II) chondrule, and a representative number of FeO‐poor (type I) chondrules, were studied to build a substantial and self‐consistent data set. The average abundances and standard deviations of Cr₂O₃ in FeO‐rich olivine phenocrysts are consistent with previous work that the CR chondrites are among the least thermally altered samples from the early solar system. Type II chondrules from the CR chondrites formed under highly variable conditions (e.g., precursor composition, redox conditions, cooling rate), with each chondrule recording a distinct igneous history. The opaque minerals within type II chondrules are consistent with formation during chondrule melting and cooling, starting as S‐ and Ni‐rich liquids at 988–1350 °C, then cooling to form monosulfide solid solution (mss) that crystallized around olivine/pyroxene phenocrysts. During cooling, Fe,Ni‐metal crystallized from the S‐ and Ni‐rich liquid, and upon further cooling mss decomposed into pentlandite and pyrrhotite, with pentlandite exsolving from mss at 400–600 °C. The composition, texture, and inferred formation temperature of pentlandite within chondrules studied here is inconsistent with formation via aqueous alteration. However, some opaque minerals (Fe,Ni‐metal versus magnetite and panethite) present in type II chondrules are a proxy for the degree of whole‐rock aqueous alteration. The texture and composition of sulfide‐bearing opaque minerals in Graves Nunataks 06100 and Grosvenor Mountains 03116 suggest that they are the most thermally altered CR chondrites.     

Multiple melting in a four‐layered barred‐olivine chondrule with compositionally heterogeneous glass from LL3.0 Semarkona

Chondrule K7p from LL3.0 Semarkona consists of four nested barred‐olivine (BO) chondrules. The innermost BO chondrule (chondrule 1) formed by complete melting of an olivine‐rich dustball. After formation, the chondrule was incorporated into another olivine‐rich dustball. A second heating event caused this second dustball to melt; the mesostasis and some of the olivine in chondrule 1 were probably also melted at this time, but the chondrule 1 structure remained largely intact. At this stage, the object was an enveloping compound BO chondrule. This two‐step process of melting and dustball enshrouding repeated two more times. The different proportions of olivine and glass in chondrules 1–4 suggest that the individual precursor dustballs differed in the amounts of chondrule fragments they contained and the mineral proportions in those fragments. The final dustball (which ultimately formed chondrule 4) was somewhat more ferroan; after melting, crystallizing, and quenching, chondrule 4 contained olivine and glass with higher FeO and MnO contents than those of the earlier formed chondrules. Subsequent aqueous alteration on the LL parent body transformed the abundant metal blebs and stringers at the chondrule surface into carbide, iron oxide, and minor Ni‐rich metal. Portions of the mesostasis underwent dissolution, producing holes and adjacent blades of more resistant material. Much of the glass in the chondrule remained isotropic, even after minor hydration and leaching. The sharp, moderately lobate boundary between the extensively altered mesostasis and the isotropic glass represents the reaction front beyond which there was little or no glass dissolution.     

Gas‐melt interactions and their bearing on chondrule formation

Abstract— Interactions between nebular gas and molten silicates or oxides could have played a major role in the formation and differentiation of the first solids formed in the solar system. In order to simulate such interactions, we set up a new experimental device in which isothermal condensation experiments have been conducted. Partially molten chondrule‐like samples have been exposed to high SiO(g) partial pressures, for intervals between 80 and 300 s and at temperatures ranging from 1600 to 1750 K. Results show that silica entering from the gas phase could be responsible for several textural and mineralogical features observed in natural chondrules. For instance, these experiments reproduce not only the mineralogical zonation of porphyritic olivine‐pyroxene chondrules with the peripheral location of pyroxenes, but also olivine resorption textures and the common poikilitical enclosure of olivines in pyroxenes. In the light of these similarities, we advocate that gas‐melt interactions through condensation are viable mechanisms for chondrule formation and hence may place severe constraints on the history of these primitive objects. In the nebula, high SiO(_g) partial pressures could have been established by the volatilization of regions with high dust/gas ratio. A possible scenario for this stochastic thermal activity is the intense activity of the protosun in its young stellar object phase.     

Nickel abundance in stony cosmic spherules: Constraining precursor material and formation mechanisms

Abstract– We report bulk and olivine compositions in 66 stony cosmic spherules (Na₂O < 0.76 wt%), 200–800 μm in size, from the Transantarctic Mountains, Antarctica. In porphyritic cosmic spherules, relict olivines that survived atmospheric entry heating are always Ni‐poor and similar in composition to the olivines in carbonaceous or unequilibrated ordinary chondrites (18 spherules), and equilibrated ordinary chondrites (one spherule). This is consistent with selective survival of high temperature, Mg‐rich olivines during atmospheric entry. Olivines that crystallized from the melts produced during atmospheric entry have NiO contents that increase with increasing NiO in the bulk spherule, and that range from values similar to those observed in chondritic olivines (NiO generally <0.5 wt%) to values characteristic of olivines in meteoritic ablation spheres (NiO > 2 wt%). Thus, NiO content in olivine cannot be used alone to distinguish meteoritic ablation spheres from cosmic spherules, and the volatile element contents have to be considered. We propose that the variation in NiO contents in cosmic spherules and their olivines is the result of variable content of Fe, Ni metal in the precursor. NiO contents in olivines and in cosmic spherules can thus be used to discuss their parent body. Ni‐poor spherules can be derived from C‐rich and/or metal‐poor precursors, either related to CM, CI, CR chondrites or to chondritic fragments dominated by silicates, regardless of the parent body. Ni‐rich spherules (NiO > 0.7 wt%) that represent 55% of the 47 barred‐olivine spherules we studied, were derived from the melting of C‐poor, metal‐rich precursors, compatible with ordinary chondrite or CO, CV, CK carbonaceous chondrite parentages.     

The Isheyevo meteorite: Mineralogy,petrology, bulk chemistry,oxygen, nitrogen,carbon isotopic compositions,and 40Ar‐39Ar ages

Abstract— Isheyevo is a metal‐rich carbonaceous chondrite that contains several lithologies with different abundances of Fe,Ni metal (7–90 vol%). The metal‐rich lithologies with 50–60 vol% of Fe,Ni metal are dominant. The metal‐rich and metal‐poor lithologies are most similar to the CB_b and CH carbonaceous chondrites, respectively, providing a potential link between these chondrite groups. All lithologies experienced shock metamorphism of shock stage S4. All consist of similar components—Fe,Ni metal, chondrules, refractory inclusions (Ca, Al‐rich inclusions [CAIs] and amoeboid olivine aggregates [AOAs]), and heavily hydrated lithic clasts—but show differences in their modal abundances, chondrule sizes, and proportions of porphyritic versus non‐porphyritic chondrules. Bulk chemical and oxygen isotopic compositions are in the range of CH and CB chondrites. Bulk nitrogen isotopic composition is highly enriched in ¹⁵N (δ¹⁵N = 1122‰). The magnetic fraction is very similar to the bulk sample in terms of both nitrogen release pattern and isotopic profile; the non‐magnetic fraction contains significantly less heavy N. Carbon released at high temperatures shows a relatively heavy isotope signature. Similarly to CB_b chondrites, ～20% of Fe,Ni‐metal grains in Isheyevo are chemically zoned. Similarly to CH chondrites, some metal grains are Ni‐rich (>20 wt% Ni). In contrast to CB_b and CH chondrites, most metal grains are thermally decomposed into Ni‐rich and Ni‐poor phases. Similar to CH chondrites, chondrules have porphyritic and non‐porphyritic textures and ferromagnesian (type I and II), silica‐rich, and aluminum‐rich bulk compositions. Some of the layered ferromagnesian chondrules are surrounded by ferrous olivine or phyllosilicate rims. Phyllosilicates in chondrule rims are compositionally distinct from those in the hydrated lithic clasts. Similarly to CH chondrites, CAIs are dominated by the hibonite‐, grossite‐, and melilite‐rich types; AOAs are very rare. We infer that Isheyevo is a complex mixture of materials formed by different processes and under different physico‐chemical conditions. Chondrules and refractory inclusions of two populations, metal grains, and heavily hydrated clasts accreted together into the Isheyevo parent asteroid in a region of the protoplanetary disk depleted in fine‐grained dust. Such a scenario is consistent with the presence of solar wind—implanted noble gases in Isheyevo and with its comparatively old K‐Ar age. We cannot exclude that the K‐Ar system was affected by a later collisional event. The cosmic‐ray exposure (CRE) age of Isheyevo determined by cosmogenic ³⁸Ar is ～34 Ma, similar to that of the Bencubbin (CB_a) meteorite.     

Mineralogical characterization of primitive,type‐3 lithologies in Rumuruti chondrites

Abstract— Rumuruti (R) chondrites constitute a new, well‐established chondrite group different from the carbonaceous, ordinary, and enstatite chondrites. Many of these samples are gas‐rich regolith breccias showing the typical light‐dark structure and consist of abundant fragments of various parent‐body lithologies embedded in a fine‐grained olivine‐rich matrix. Unequilibrated type‐3 lithologies among these fragments have frequently been mentioned in various publications. In this study, detailed mineralogical data on seven primitive fragments from the R‐chondrites Dar al Gani 013 and Hughes 030 are presented. The fragments range from ～300 μ in size up to several millimeters. Generally, the main characteristics can be summarized as follows: (1) Unequilibrated type‐3 fragments have a well‐preserved chondritic texture with a chondrule‐to‐matrix ratio of ～1:1. Chondrules and chondrule fragments are embedded in a fine‐grained olivine‐rich matrix. Thus, the texture is quite similar to that of type‐3 carbonaceous chondrites. (2) In all cases, matrix olivines in type‐3 fragments have a significantly higher Fa content (44–57 mol%) than olivines in other (equilibrated) lithologies (38–40 mol% Fa). (3) Olivines and pyroxenes occurring within chondrules or as fragments are highly variable in composition (Fa_0–65 and Fs_0–33, respectively) and, generally, more magnesian than those found in equilibrated R chondrites. Agglomerated material of the R‐chondrite parent body (or bodies) was highly unequilibrated. It is suggested that the material that accreted to form the parent body consisted of chondrules and chondrule fragments, mainly having Mg‐rich silicate constituents, and Fe‐rich highly oxidized fine‐grained materials. The dominating phase of this fine‐grained material may have been Fa‐rich olivine from the beginning. The brecciated whole rocks, the R‐chondrite regolith breccias, were not significantly reheated subsequent to brecciation or during lithification, as indicated by negligible degree of equilibration between matrix components and Mg‐rich olivines and pyroxenes in primitive type‐3 fragments.     

Oxygen isotopes in chondrule olivine and isolated olivine grains from the CO3 chondrite Allan Hills A77307

Abstract— We have measured O‐isotopic ratios in a variety of olivine grains in the CO3 chondrite Allan Hills (ALH) A77307 using secondary ion mass spectrometry in order to study the chondrule formation process and the origin of isolated olivine grains in unequilibrated chondrites. Oxygen‐isotopic ratios of olivines in this chondrite are variable from δ¹⁷O = ?15.5 to +4.5% and δ¹⁸O = ?11.5 to +3.9%, with Δ¹⁷O varying from ?10.4 to +3.5%. Forsteritic olivines, Fa_<1, are enriched in ¹⁶O relative to the bulk chondrite, whereas more FeO‐rich olivines are more depleted in ¹⁶O. Most ratios lie close to the carbonaceous chondrite anhydrous minerals (CCAM) line with negative values of Δ¹⁷O, although one grain of composition Fa₄ has a mean Δ¹⁷O of +1.6%. Marked O‐isotopic heterogeneity within one FeO‐rich chondrule is the result of incorporation of relic, ¹⁶O‐rich, Mg‐rich grains into a more ¹⁶O‐depleted host. Isolated olivine grains, including isolated forsterites, have similar O‐isotopic ratios to olivine in chondrules of corresponding chemical composition. This is consistent with derivation of isolated olivine from chondrules, as well as the possibility that isolated grains are chondrule precursors. The high ¹⁶O in forsteritic olivine is similar to that observed in forsterite in CV and CI chondrites and the ordinary chondrite Julesburg and suggests nebula‐wide processes for the origin of forsterite that appears to be a primitive nebular component.     

A clast of Bali‐like oxidized CV material in the reduced CV chondrite breccia Vigarano

Abstract— The CV (Vigarano‐type) chondrites are a petrologically diverse group of meteorites that are divided into the reduced and the Bali‐like and Allende‐like oxidized subgroups largely based on secondary mineralogy (Weisberg et al., 1997; Krot et al., 1998b). Some chondrules and calcium‐aluminum‐rich inclusions (CAIs) in the reduced CV chondrite Vigarano show alteration features similar to those in Allende: metal is oxidized to magnetite; low‐Ca pyroxene, forsterite, and magnetite are rimmed and veined by ferrous olivine (Fs_40–50); and plagioclase mesostases and melilite are replaced by nepheline and sodalite (Sylvester et al., 1993; Kimura and Ikeda, 1996, 1997, 1998). Our petrographic observations indicate that Vigarano also contains individual chondrules, chondrule fragments, and lithic clasts of the Bali‐like oxidized CV materials. The largest lithic clast (about 1 times 2 cm in size) is composed of opaque matrix, type‐I chondrules (400–2000 μm in apparent diameter) surrounded by coarse‐grained and fine‐grained rims, and rare CAIs. The matrix‐chondrule ratio is about 1.1. Opaque nodules in chondrules in the clast consist of Cr‐poor and Cr‐rich magnetite, Ni‐ and Co‐rich metal, Ni‐poor and Ni‐rich sulfide; low‐Ni metal nodules occur only inside chondrule phenocrysts. Chromium‐poor magnetite is preferentially replaced by fayalite. Chondrule mesostases are replaced by phyllosilicates; low‐Ca pyroxene and olivine phenocrysts appear to be unaltered. Matrix in the clast consists of very fine‐grained (<1 μm) ferrous olivine, anhedral fayalite grains (Fa_80–100), rounded objects of porous Ca‐Fe‐rich pyroxenes (Fs_10–50Wo₅₀), Ni‐poor sulfide, Ni‐ and Co‐rich metal, and phyllosilicates; magnetite is rare. On the basis of the presence of the Bali‐like lithified chondritic clast—in addition to individual chondrules and CAIs of both Bali‐like and Allende‐like materials—in the reduced CV chondrite Vigarano, we infer that (1) all three types of materials were mixed during regolith gardening on the CV asteroidal body, and (2) the reduced and oxidized CV materials may have originated from a single, heterogeneously altered asteroid.     

Shock melts in QUE 94411, Hammadah al Hamra 237, and Bencubbin: Remains of the missing matrix?

Abstract— We have studied the CB carbonaceous chondrites Queen Alexandra Range (QUE) 94411, Hammadah al Hamra (HH) 237, and Bencubbin with an emphasis on the petrographical and mineralogical effects of the shock processing that these meteorite assemblages have undergone. Iron‐nickel metal and chondrule silicates are the main components in these meteorites. These high‐temperature components are held together by shock melts consisting of droplets of dendritically intergrown Fe,Ni‐metal/sulfide embedded in silicate glass, which is substantially more FeO‐rich (30–40 wt%) than the chondrule silicates (FeO <5 wt%). Fine‐grained matrix material, which is a major component in most other chondrite classes, is extremely scarce in QUE 94411 and HH 237, and has not been observed in Bencubbin. This material occurs as rare, hydrated matrix lumps with major and minor element abundances roughly similar to the ferrous silicate shock melts (and CI). We infer that hydrated, fine‐grained material, compositionally similar to these matrix lumps, was originally present between the Fe,Ni‐metal grains and chondrules, but was preferentially shock melted. Other shock‐related features in QUE 94411, HH 237, and Bencubbin include an alignment and occasionally strong plastic deformation of metal and chondrule fragments. The existence of chemically zoned and metastable Fe,Ni‐metal condensates in direct contact with shock melts indicates that the shock did not substantially increase the average temperature of the rock. Because porphyritic olivine‐pyroxene chondrules are absent in QUE 94411, HH 237, and Bencubbin, it is difficult to determine the precise shock stage of these meteorites, but the shock was probably relatively light (S2–S3), consistent with a bulk temperature increase of the assemblages of less than ?300 °C. The apparently similar shock processing of Bencubbin, Weatherford, Gujba (CB_a) and QUE 94411/HH 237 (CB_b) supports the idea of a common asteroidal parent body for these meteorites.     

Opaque minerals in chondrules and fine‐grained chondrule rims in the Bishunpur (LL3.1) chondrite

Abstract— We present a detailed petrographic and electron microprobe study of metal grains and related opaque minerals in the chondrule interiors and rims of the Bishunpur (LL3.1) ordinary chondrite. There are distinct differences between metal grains that are completely encased in chondrule interiors and those that have some portion of their surface exposed outside of the chondrule boundary, even though the two types of metal grains can be separated by only a few microns. Metal grains in chondrule interiors exhibit minor alteration in the form of oxidized P‐, Cr‐, and Si‐bearing minerals. Metal grains at chondrule boundaries and in chondrule rims are extensively altered into troilite and fayalite. The results of this study suggest that many metal grains in Bishunpur reacted with a type‐I chondrule melt and incorporated significant amounts of P, Cr, and Si. As the system cooled, some metal oxidation occurred in the chondrule interior, producing metal‐associated phosphate, chromite, and silica. Metal that migrated to chondrule boundaries experienced extensive corrosion as a result of exposure to the external atmosphere present during chondrule formation. It appears that chondrule‐derived metal and its corrosion products were incorporated into the fine‐grained rims that surround many type‐I chondrules, contributing to their Fe‐rich compositions. We propose that these fine‐grained rims formed by a combination of corrosion of metal expelled from the chondrule interior and accretion of fine‐grained mineral fragments and microchondrules.     

Silica‐rich objects in the Acfer 182 CH chondrite: A new view

Five silica‐rich objects (SRO) from Acfer 182 were studied. They have cryptocrystalline textures characterized by micro‐emulsion and amoeboid patterns that point toward the coexistence of pyroxene‐ and silica‐normative liquids that were quenched. Both objects have variable contents of refractory lithophile elements. Their positive Yb versus La correlation around primordial values suggests a cosmochemical process (e.g., a gas/liquid condensation) as responsible for SRO formation. The bulk trace element abundances of amoeboid‐ and emulsion‐type SRO as well as their fractionation do not support an origin through high temperature processes. Conversely, their formation might have taken place while cooling of the nebular gas in two different chondrule‐forming regions characterized by having different evolution paths. Cooling of these dust‐enriched regions might lead to the condensation of pyroxene‐rich liquids first, followed by formation of Mg‐rich and SiO₂‐rich liquids, provided irradiation and annealing were active in these regions. Irradiation could be the process involved both in the formation of cristobalite (with annealing ~1200 K) and in triggering a spinoidal decomposition causing unmixing of the enstatite liquid into two coexisting phases, such as Mg‐rich and SiO₂‐rich liquids, the precursors of the SRO in Acfer 182. Formation of emulsion‐ and amoeboid‐type objects may be the result of exposing those chondrule‐forming regions to different degrees of radiation.     

Kosmochloric Ca‐rich pyroxenes and FeO‐rich olivines (Kool grains) and associated phases in Stardust tracks and chondritic porous interplanetary dust particles: Possible precursors to FeO‐rich type II chondrules in ordinary chondrites

Abstract— Terminal particles and mineral fragments from comet 81P/Wild 2 were studied in 16 aerogel tracks by transmission and secondary electron microscopy. In eight tracks clinopyroxenes with correlated Na₂O and Cr₂O₃ contents as high as 6.0 wt% and 13.0 wt%, respectively, were found. Kosmochloric (Ko) clinopyroxenes were also observed in 4 chondritic interplanetary dust particles (IDPs). The Ko‐clinopyroxenes were often associated with FeO‐rich olivine ± Cr‐rich spinel ± aluminosilicate glass or albitic feldspar, assemblages referred to as Kool grains (Ko = kosmochloric Ca‐rich pyroxene, ol = olivine). Fine‐grained (submicron) Kool fragments have textures suggestive of crystallization from melts while coarse‐grained (>1 μm) Kool fragments are often glass‐free and may have formed by thermal metamorphism in the nebula. Average major and minor element distributions between clinopyroxenes and coexisting FeO‐rich olivines are consistent with these phases forming at or near equilibrium. In glass‐bearing fine‐grained Kool fragments, high concentrations of Na in the clinopyroxenes are inconsistent with existing experimentally determined partition coefficients at equilibrium. We speculate that the availability of Cr in the melt increased the clinopyroxene Na partition coefficient via a coupled substitution thereby enhancing this phase with the kosmochlor component. The high temperature minerals, fine‐grain sizes, bulk compositions and common occurrence in the SD tracks and IDPs support the idea that Kool grains could have been precursors to type II chondrules in ordinary chondrites. These grains, however, have not been observed in these meteorites suggesting that they were destroyed during chondrule formation and recycling or were not present in the nebula at the time and location where meteoritic chondrules formed.     

Mineralogy of fine‐grained material in the Krymka (LL3.1) chondrite

Abstract— Two dark lithic fragments and matrix of the Krymka LL3.1 chondrite were mineralogically and chemically studied in detail. These objects are characterised by the following chemical and mineralogical characteristics, which distinguish them from the host chondrite Krymka: (1) bulk chemical analyses revealed low totals (systematically lower than 94 wt%) due to high porosity; (2) enrichment in FeO and depletion in S, MgO and SiO₂ due to a high abundance of Fe‐rich silicates and low sulfide abundance; (3) fine‐grained, almost chondrule‐free texture with predominance of a porous, cryptocrystalline groundmass and fine grains; (4) occurrence of a small amount of once‐molten material (microchondrules) enclosed in fine‐grained materials; (5) occurrence of accretionary features, especially unique accretionary spherules; (6) high abundance of small calcium‐ aluminium‐rich inclusions (CAIs) in one of the fine‐grained fragments. It is suggested that the abundance of CAIs in this fragment is one of the highest ever found in an ordinary chondrite. Accretionary, fine‐grained spherules within one of the fragments bear fundamental information about the initial stages of accretion as well as on the evolution of the clast, its incorporation, and history within the bulk rock of Krymka. The differences in porosity, bulk composition, and mineralogy of cores and rims of the fine‐grained spherulitic objects allow us to speculate on the following processes: (1) Low velocity accretion of tiny silicate grains onto the surface of coarse metal or silicate grains in a dusty region of the nebula is the beginning of the formation of accretionary, porous (fluffy) silicate spherules. (2) Within a dusty environment with decreasing silicate/(metal + sulfide) ratio the porous spherules collected abundant metal and sulfide particles together with silicate dust, which formed an accretionary rim. Variations of the silicate/(sulfide + metal) ratio in the dusty nebular environment result in the formation of multi‐layered rims on the surface of the silicate‐rich spherules. (3) Soft accretion and lithification of rimmed, fluffy spherules, fine‐grained, silicate‐rich dust, metal‐sulfide particles, CAIs, silicate‐rich microchondrules, and coarse silicate grains and fragments followed. (4) After low‐temperature processing of the primary, accretionary rock collisional fragmentation occurred, the fragments were subsequently coated by fine‐grained material, which was highly oxidized and depleted in sulfides. (5) In a final stage this accretionary “dusty” rock was incorporated as a fragment within the Krymka host.     

Refractory inclusions in the CH/CB‐like carbonaceous chondrite Isheyevo: I. Mineralogy and petrography

Abstract— –The CH/CB‐like chondrite Isheyevo consists of metal‐rich (70–90 vol% Fe,Ni‐metal) and metal‐poor (7–20 vol% Fe,Ni‐metal) lithologies which differ in size and relative abundance of Fe,Ni‐metal and chondrules, as well as proportions of porphyritic versus non‐porphyritic chondrules. Here, we describe the mineralogy and petrography of Ca,Al‐rich inclusions (CAIs) and amoeboid olivine aggregates (AOAs) in these lithologies. Based on mineralogy, refractory inclusions can be divided into hibonite‐rich (39%), grossite‐rich (16%), melilite‐rich (19%), spinel‐rich (14%), pyroxene‐anorthite‐rich (8%), fine‐grained spinel‐rich CAIs (1%), and AOAs (4%). There are no systematic differences in the inclusion types or their relative abundances between the lithologies. About 55% of the Isheyevo CAIs are very refractory (hibonite‐rich and grossite‐rich) objects, 20–240 μm in size, which appear to have crystallized from rapidly cooling melts. These inclusions are texturally and mineralogically similar to the majority of CAIs in CH and CB chondrites. They are distinctly different from CAIs in other carbonaceous chondrite groups dominated by the spinel‐pyroxene ± melilite CAIs and AOAs. The remaining 45% of inclusions are less refractory objects (melilite‐, spinel‐ and pyroxene‐rich CAIs and AOAs), 40–300 μm in size, which are texturally and mineralogically similar to those in other chondrite groups. Both types of CAIs are found as relict objects inside porphyritic chondrules indicating recycling during chondrule formation. We infer that there are at least two populations of CAIs in Isheyevo which appear to have experienced different thermal histories. All of the Isheyevo CAIs apparently formed at an early stage, prior to chondrule formation and prior to a hypothesized planetary impact that produced magnesian cryptocrystalline and skeletal chondrules and metal grains in CB, and possibly CH chondrites. However, some of the CAIs appear to have undergone melting during chondrule formation and possibly during a major impact event. We suggest that Isheyevo, as well as CH and CB chondrites, consist of variable proportions of materials produced by different processes in different settings: 1) by evaporation, condensation, and melting of dust in the protoplanetary disk (porphyritic chondrules and refractory inclusions), 2) by melting, evaporation and condensation in an impact generated plume (magnesian cryptocrystalline and skeletal chondrules and metal grains; some igneous CAIs could have been melted during this event), and 3) by aqueous alteration of pre‐existing planetesimals (heavily hydrated lithic clasts). The Isheyevo lithologies formed by size sorting of similar components during accretion in the Isheyevo parent body; they do not represent fragments of CH and CB chondrites.     

Evidence for fractional condensation and reprocessing at high temperatures in CH chondrites

Abstract— We performed a detailed study of silica‐rich components (SRC) in the paired CH chondrites Acfer 182 and 207. These SRCs appear either as chondrules or fragments, and they contribute <0.1 vol% to the bulk meteorite. They usually contain a silica and a silicate portion. Both portions are, in most cases, cryptocrystalline and have bulk SiO₂‐concentrations between 65 and 85 wt%. The silicate generally has a pyroxene normative composition. The silica often appears as blebs within the silicate matrix or vice versa. If there are no blebs, silica and silicate still form rounded interfaces. The SRCs are depleted in refractory elements like Ca, Al, and Ti relative to CI. A few SRC‐like objects are extremely rich in Mn and show no depletion in refractory elements. We conducted micro‐Raman studies on the silica portions of the SRCs to determine their structure, and we identified several silica phases: α‐quartz, cristobalite, glass, and a yet unidentified polymorph. The silicate portion is glass when the silica is glass and crystalline when the silica is crystalline. The low contents of Al and Ca make an igneous origin of the SRCs very unlikely, and the absence of metal excludes the formation by reduction of pyroxene. We suggest, instead, a fractional condensation origin of the SRCs from a Si‐enriched gas after removal of gaseous Mg by forsterite condensation. Additional evidence for fractional condensation is provided by a unique layered object with olivine in the core, pyroxene and metal at the rim, and silica at the outermost border; these layers record the condensation sequence. Two chondrules were found with several percent of Mn and high Cr, Na, and K contents, providing further evidence for condensation from a fractionated gas. The texture of the SRCs and the occurrence of cristobalite and silica glass, however, require formation by liquid immiscibility at high temperatures, above 1968 K, and subsequent fast cooling. Therefore, we propose a 2‐stage model for the formation of SRCs in CH chondrites: 1) fractional condensation of forsterite, enstatite, and SiO₂‐rich phases; and 2) reheating of SiO₂‐rich components to temperatures above 1968 K followed by rapid cooling. All other phases identified in CH chondrites can be understood within the framework of this model. Thus, the extremely unequilibrated CH chondrites provide a wealth of evidence for fractional condensation processes in the early solar nebula, in metals (Meibom et al. 1999), and in silicates.     

Trace element geochemistry of CR chondrite metal

We report trace element analyses by laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) of metal grains from nine different CR chondrites, distinguishing grains from chondrule interior (“interior grains”), chondrule surficial shells (“margin grains”), and the matrix (“isolated grains”). Save for a few anomalous grains, Ni‐normalized trace element patterns are similar for all three petrographic settings, with largely unfractionated refractory siderophile elements and depleted volatile Au, Cu, Ag, S. All three types of grains are interpreted to derive from a common precursor approximated by the least‐melted, fine‐grained objects in CR chondrites. This also excludes recondensation of metal vapor as the origin of the bulk of margin grains. The metal precursors were presumably formed by incomplete condensation, with evidence for high‐temperature isolation of refractory platinum‐group‐element (PGE)‐rich condensates before mixing with lower temperature PGE‐depleted condensates. The rounded shape of the Ni‐rich, interior grains shows that they were molten and that they equilibrated with silicates upon slow cooling (1–100 K h^?1), largely by oxidation/evaporation of Fe, hence their high Pd content, for example. We propose that Ni‐poorer, amoeboid margin grains, often included in the pyroxene‐rich periphery common to type I chondrules, result from less intense processing of a rim accreted onto the chondrule subsequent to the melting event recorded by the interior grains. This means either that there were two separate heating events, which formed olivine/interior grains and pyroxene/margin grains, respectively, between which dust was accreted around the chondrule, or that there was a single high‐temperature event, of which the chondrule margin records a late “quenching phase,” in which case dust accreted onto chondrules while they were molten. In the latter case, high dust concentrations in the chondrule‐forming region (at least three orders of magnitude above minimum mass solar nebula models) are indicated.     

Secondary‐volatiles linked metallic iron in eucrites: The dual‐origin metals of Camel Donga

The unique occurrence of abundant (~1 vol%) near‐pure‐Fe metal in the Camel Donga eucrite is more complicated than previously believed. In addition to that component of groundmass metal, scattered within the meteorite are discrete nodules of much higher kamacite abundance. We have studied the petrology and composition of two of these nodules in the form of samples we call CD2 and CD3. The nodules are ovoids 11 (CD2) to 15 (CD3) mm across, with metal, or inferred preweathering metal, abundances of 12–17 vol% (CD2 is unfortunately quite weathered). The CD3 nodule also includes at its center a 5 mm ovoid clumping (6 vol%) of F‐apatite. Both nodules are fine‐grained, so the high Fe metal and apatite contents are clearly not flukes of inadequate sampling. The metals within the nodules are distinctly Ni‐rich (0.3–0.6 wt%) compared to the pure‐Fe (Ni generally 0.01 wt%) groundmass metals. Bulk analyses of three pieces of the CD2 nodule show that trace siderophile elements Ir, Os, and Co are commensurately enriched; Au is enriched to a lesser degree. The siderophile evidence shows the nodules did not form by in situ reduction of pyroxene FeO. Moreover, the nodules do not show features such as silica‐phase enrichment or pyroxene with reduced FeO (as constrained by FeO/MgO and especially FeO/MnO) predicted by the in situ reduction model. The oxide minerals, even in groundmass samples well away from the nodules, also show little evidence of reduction. Although the nodule boundaries are generally sharp, groundmass‐metal Ni content is anti‐correlated with distance from the CD3 nodule. We infer that the nodules represent materials that originated within impactors into the Camel Donga portion of the eucrite crust, but probably were profoundly altered during later metamorphism/metasomatism. Origin of the pure‐Fe groundmass metal remains enigmatic. In situ reduction probably played an important role, and association in the same meteorite of the Fe‐nodules is probably significant. But the fluid during alteration was probably not (as previously modeled) purely S and O, of simple heat‐driven internal derivation. We conjecture a two‐stage metasomatism, as fluids passed through Camel Donga after impact heating of volatile‐rich chondritic masses (survivors of gentle accretionary impacts) within the nearby crust. First, reduction to form troilite may have been triggered by fluids rich in S₂ and CO (derived from the protonodules?), and then in a distinct later stage, fluids were (comparatively) H₂O‐rich, and thus reacted with troilite to form pure‐Fe metal along with H₂S and SO₂. The early eucrite crust was in places a dynamic fluid‐bearing environment that hosted complex chemical processes, including some that engendered significant diversity among metal+sulfide alterations.     

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.