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.     

Size‐frequency distributions of chondrules and chondrule fragments in LL3 chondrites: Implications for parent‐body fragmentation of chondrules

Abstract— We measured the sizes and textural types of 719 intact chondrules and 1322 chondrule fragments in thin sections of Semarkona (LL3.0), Bishunpur (LL3.1), Krymka (LL3.1), Piancaldoli (LL3.4) and Lewis Cliff 88175 (LL3.8). The mean apparent diameter of chondrules in these LL3 chondrites is 0.80 φ units or 570 μm, much smaller than the previous rough estimate of ～900 μm. Chondrule fragments in the five LL3 chondrites have a mean apparent cross‐section of 1.60 φ units or 330 μm. The smallest fragments are isolated olivine and pyroxene grains; these are probably phenocrysts liberated from disrupted porphyritic chondrules. All five LL3 chondrites have fragment/ chondrule number ratios exceeding unity, suggesting that substantial numbers of the chondrules in these rocks were shattered. Most fragmentation probably occurred on the parent asteroid. Porphyritic chondrules (porphyritic olivine + porphyritic pyroxene + porphyritic olivine‐pyroxene) are more readily broken than droplet chondrules (barred olivine + radial pyroxene + cryptocrystalline). The porphyritic fragment/chondrule number ratio (2.0) appreciably exceeds that of droplet‐textured objects (0.9). Intact droplet chondrules have a larger mean size than intact porphyritic chondrules, implying that large porphyritic chondrules are fragmented preferentially. This is consistent with the relatively low percentage of porphyritic chondrules within the set of the largest chondrules (57%) compared to that within the set of the smallest chondrules (81%). Differences in mean size among chondrule textural types may be due mainly to parent‐body chondrule‐fragmentation events and not to chondrule‐formation processes in the solar nebula.     

Evidence in CO3.0 chondrules for a drift in the O isotopic composition of the solar nebula

Abstract— Several recent studies have shown that materials such as magnetite that formed in asteroids tend to have higher Δ¹⁷O (=δ¹⁷O ? 0.52 × δ¹⁸O) values than those recorded in unaltered chondrules. Other recent studies have shown that, in sets of chondrules from carbonaceous chondrites, Δ¹⁷O tends to increase as the FeO contents of the silicates increase. We report a comparison of the O isotopic composition of olivine phenocrysts in low‐FeO (≤Fa₁) type I and high‐FeO (≥Fa₁₅) type II porphyritic chondrules in the highly primitive CO3.0 chondrite Yamato‐81020. In agreement with a similar study of chondrules in CO3.0 ALH A77307 by Jones et al. (2000), Δ¹⁷O tends to increase with increasing FeO. We find that Δ¹⁷O values are resolved (but only marginally) between the two sets of olivine phenocrysts. In two of the high‐FeO chondrules, the difference between Δ¹⁷O of the late‐formed, high‐FeO phenocryst olivine and those in the low‐FeO cores of relict grains is well‐resolved (although one of the relicts is interpreted to be a partly melted amoeboid olivine inclusion by Yurimoto and Wasson [2002]). It appears that, during much of the chondrule‐forming period, there was a small upward drift in the Δ¹⁷O of nebular solids and that relict cores preserve the record of a different (and earlier) nebular environment.     

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.     

Ordinary (mesostasis) and not‐so‐ordinary (symplectites) late‐stage assemblages in howardites

Abstract– Two categories of symplectites have been observed in howardites: three‐phase, composed of vermicular intergrowths of ferroan augite, fayalitic olivine, and silica, and two‐phase, composed of vermicular intergrowths of orthopyroxene and troilite. Three‐phase symplectites have been previously shown to represent the breakdown products of metastable pyroxene. In howardites, they appear to be genetically related to gabbroic eucrites. In some cases and under yet‐to‐be specified conditions, ferroan clinopyroxene in gabbroic eucrites may undergo only localized decomposition resulting in oriented exsolution‐like features. Breakdown phases in those cases are fayalitic olivine, silica, and—depending on the MgO content of the system—orthopyroxene. As opposed to three‐phase symplectites, two‐phase symplectites are most likely of diogenitic origin. They probably formed via impact‐induced localized melting of diogenitic orthopyroxene in the presence of troilite (grain boundary melting). Three‐phase symplectites in howardites occasionally contain accessory amounts of ilmenite, troilite, and/or kamacite and are exclusively associated with medium‐grained FeO‐rich pyroxene, silica, and plagioclase. All minerals involved are late‐stage crystallites or mesostasis phases. In general, highly evolved eucritic lithologies constitute only a minor fraction of howardites. However, considering that three‐phase symplectites are generated in a low‐pressure, i.e., near‐surface, environment, FeO‐ and CaO‐rich eucritic rocks may be exposed locally on Vesta’s surface. This, in turn, is highly relevant to the ongoing DAWN mission.     

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.     

Origin of a unique impact-melt rock—the L-chondrite Ramsdorf

Abstract— We have studied a unique impact-melt rock, the Ramsdorf L chondrite, using optical and scanning microscopy and electron microprobe analysis. Ramsdorf contains not only clast-poor impact melt (Begemann and Wlotzka, 1969) but also a chondritic portion (>60 g) with what appears at low magnification to be a normal, well-defined chondritic texture. However, detailed studies at high magnification show that >90 vol% of the crystals in the chondritic portion were largely melted by the impact: the chondrules lack normal microtextures and are ghosts of the original features. The only relics from the precursor chondrules are olivine crystals, which have the highest melting temperature (～1620 °C). Pyroxene-rich chondrules were so extensively melted that no phenocrysts were preserved and the melt crystallized in situ before significant mixing with exterior olivine-rich melts. Fine-grained pyroxene chondrule ghosts have sharper boundaries with the matrix than porphyritic olivine and pyroxene chondrule ghosts, probably because pyroxene-rich melts are significantly more viscous. Complex textures that formed by injection of melt along cracks and fractures in relic olivines suggest that the chondritic portion of Ramsdorf formed directly from petrologic type 3–4 material by strong shock. We infer that Ramsdorf was largely melted by shock pressures of ～75–90 GPa and that chondrule ghosts and relic olivine phenocrysts were locally preserved by rapid cooling. Quenching was not due to the addition of cold clasts into the melt but to heterogeneous shock heating that only caused internal melting of large olivines and pyroxenes. Ramsdorf appears to be one of the most heavily shocked meteorites that has retained some trace of its original texture.     

Petrology and mineralogy of the angrite Northwest Africa 1670

Abstract— Northwest Africa (NWA) 1670, contains olivines of up to 5 mm in size representing about 30% of the studied section. With subordinate clinopyroxene and chrome‐spinel microphenocrysts (0.2‐0.5 mm), they represent a xenocrystic association. Phenocrysts are surrounded by a groundmass, predominantly comprising bundles of plagioclase and clinopyroxene (typically 20 × 200 μm crystals). Olivine and kirschsteinite are present in the groundmass in lesser amounts. The olivine xenocrysts (Fo90) are significantly fractured and show mosaicism for their major part, the remaining showing faint undulatory extinction. They are surrounded with a rim of 100–200 μm zoned down to Fo80 and overgrown with serrated olivine, Fo80 to Fo60 (about 100 μm). Olivine in the groundmass is zoned from Mg# 0.55 to 0.15; its CaO content ranges 2.0 to 8.4%. Subcalcic kirschsteinite is zoned from Mg# 0.13 to 0.03, CaO increasing from 15.8 to 21.3%. Pyroxenes xenocrysts (Mg# = 0.77) are superseded in the groundmass by less magnesian pyroxenes, Mg# 0.61 to 0.17, with an average FeO/ MnO of 98. Their compositions range from En₃₀ Fs₂₂ Wo₂₇ Al‐Ts₂₈ Ti‐Ts₂ to En₂ Fs₃₇ Wo₂₂ Al‐Ts₄₀ Ti‐Ts₁. Anorthite microcrysts (An99‐100) are restricted to the groundmass. Accessories are pyrrhotite, kamacite, Ca‐phosphate, titanomagnetite, hercynite and Ca‐carbonate. The bulk chemical composition confirms that NWA 1670 corresponds to a normal angrite melt that incorporated olivine. High Mg olivine xenocrysts and the associated mineralogy are typical of angrites. We suggest that it is an impact melt with relict phenocrysts. The strong silica undersaturation, the presence of Fo90 olivine xenocrysts and carbonate support their derivation as melilite‐like melts in the presence of carbonate.     

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.     

Varre-Sai: The Recent Brazilian Fall

Varre-Sai, the most recent Brazilian meteorite fall, on June 19th, 2010 at Varre-Sai, in Rio de Janeiro State, Brazil (20°51??41??S; 41°44??.80??W). At least eight masses (total ~3.5?kg) were recovered. Most are totally covered by fusion crust. The exposed interior is of light-grey colour with a few dark shock veins. Five thin polished and etched sections were prepared from a slice weighing 35?g on deposit at the National Museum/UFRJ. It consists mostly of chondrules ranging in size from 0.35 to ~2.2?mm, and chondrule fragments enclosed in a crystalline matrix. The matrix consists of tiny isolated subhedral and anhedral crystals and opaque minerals that are intergrown with broken chondrules. The chondritic texture is poorly defined with chondrule textures that vary from non-porphyritic to porphyritic ones. The essential minerals are olivine (Fa_25±0.2) and low-Ca pyroxene (Fa_21.66±0.2Wo_1.4). Accessory minerals are plagioclase, apatite, Fe?CNi metal phases, troilite, chromite and magnetite. M?ssbauer spectroscopy analysis confirms that the mineral phases are olivine, pyroxene, troilite and kamacite/taenite. Chemical data indicate that Varre-Sai is a member of the low iron L chondrite group. The observed texture and mineral phases led us to classify Varre-Sai as an equilibrated petrologic type 5. The shock features of the minerals (undulatory extinction, planar structure and numerous cracks), as well as plagioclase partial or totally transformed to maskelynite, suggest a shock stage S4. Also, some post-impact metamorphic processes could be inferred from the meta-sulfide conjoint grains that show complex mixtures of kamacite?Ctaenite?Ctetrataenite and troilite. The occurrence of veins crosscutting the studied sections indicates that Varre-Sai was affected by a late fracturing event. Sealing of these fractures must have been a fast process, as shown by troilite globule textures pointing towards rapid solidification. The meteorite name was approved by the Nomenclature Committee of the Meteoritical Society (Meteoritic Bulletin, no 99).     

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.     

Petrographic classification of Middle Ordovician fossil meteorites from Sweden

Abstract— The maximum diameter of chromite (FeCr₂O₄) grains within L chondrites reflects the petrographic type of the sample. On the basis of our measurements of nine recent L chondrites, L3 chromite D_max = 34–50 μm, L4 = 87–150 μm, L5 = 76–158 μm, and L6 = 253–638 μm. This variation reflects the crystallization of the chromite grains during parent body thermal metamorphism. We use this calibration to classify six fossil meteorites from the Middle Ordovician in Sweden as type 3 (or 4) to 6. The high flux of L chondrites at 470 Ma contained a range of petrographic types and may have had a higher proportion of lower petrographic type meteorites than are found in recent L chondrite falls. The fossil meteorites have in places preserved recognizable chondrule textures, including porphyritic olivine, barred olivine, and radiating pyroxene. A large relict clast and fusion crust have also been tentatively identified in one fossil meteorite. Apart from chromite, all of the original meteorite minerals have been replaced by carbonate (and sheet silicate and sulfate) during diagenesis within the limestone host. The preservation of chondrule definition has allowed us to measure the mean diameters of relict chondrules. The range (0.4–0.6 mm) is consistent with measurements made in the same way on recent L chondrites.     

Mineralogy,petrology, and oxygen isotopic compositions of chondritic and achondritic lithologies in the anomalous CB carbonaceous chondrites Sierra Gorda 013 and Fountain Hills

The CB (Bencubbin-like) metal-rich carbonaceous chondrites are subdivided into the CB_a and CB_b subgroups. The CB_a chondrites are composed predominantly of ~cm-sized skeletal olivine chondrules and unzoned Fe,Ni-metal ± troilite nodules. The CB_b chondrites are finer grained than the CB_as and consist of chemically zoned and unzoned Fe,Ni-metal grains, Fe,Ni-metal ± troilite nodules, cryptocrystalline and skeletal olivine chondrules, and rare refractory inclusions. Both subgroups contain exceptionally rare porphyritic chondrules and no interchondrule fine-grained matrix, and are interpreted as the products of a gas–melt impact plume formed by a high-velocity collision between differentiated planetesimals about 4562 Ma. The anomalous metal-rich carbonaceous chondrites, Fountain Hills and Sierra Gorda 013 (SG 013), have bulk oxygen isotopic compositions similar to those of other CBs but contain coarse-grained igneous clasts/porphyritic chondrule-like objects composed of olivine, low-Ca-pyroxene, and minor plagioclase and high-Ca pyroxene as well as barred olivine and skeletal olivine chondrules. Cryptocrystalline chondrules, zoned Fe,Ni-metal grains, and interchondrule fine-grained matrix are absent. In SG 013, Fe,Ni-metal (~80 vol%) occurs as several mm-sized nodules; magnesiochromite (Mg-chromite) is accessory; daubréelite and schreibersite are minor; troilite is absent. In Fountain Hills, Fe,Ni-metal (~25 vol%) is dispersed between chondrules and silicate clasts; chromite and sulfides are absent. In addition to a dominant chondritic lithology, SG 013 contains a chondrule-free lithology composed of Fe,Ni-metal nodules (~25 vol%), coarse-grained olivine and low-Ca pyroxene, interstitial high-Ca pyroxene and anorthitic plagioclase, and Mg-chromite. Here, we report on oxygen isotopic compositions of olivine, low-Ca pyroxene, and ±Mg-chromite in Fountain Hills and both lithologies of SG 013 measured in situ using an ion microprobe. Oxygen isotope compositions of olivine, low-Ca pyroxene, and Mg-chromite in these meteorites are similar to those of magnesian non-porphyritic chondrules in CB_a and CB_b chondrites: on a three-isotope oxygen diagram (δ¹⁷O vs. δ¹⁸O), they plot close to a slope-1 (primitive chondrule mineral) line and have a very narrow range of Δ¹⁷O (=δ¹⁷O–0.52 × δ¹⁸O) values, −2.5 ± 0.9‰ (avr ± 2SD). No isotopically distinct relict grains have been identified in porphyritic chondrule-like objects. We suggest that magnesian non-porphyritic (barred olivine, skeletal olivine, cryptocrystalline) chondrules in the CB_as, CB_bs, and porphyritic chondrule-like objects in SG 013 and Fountain Hills formed in different zones of the CB impact plume characterized by variable pressure, temperature, cooling rates, and redox conditions. The achondritic lithology in SG 013 represents fragments of one of the colliding bodies and therefore one of the CB chondrule precursors. Fountain Hills was subsequently modified by impact melting; Fe,Ni-metal and sulfides were partially lost during this process.     

Oxide‐bearing and FeO‐rich clasts in aubrites

Abstract— We report the occurrence of an oxide‐bearing clast and an FeO‐rich clast from aubrites. The FeO‐rich clast in Pesyanoe is dominated by olivine and pyroxene phenocrysts with mineral compositions slightly less FeO‐rich than is typical for H chondrites. In Allan Hills (ALH) 84008, the oxide‐bearing clast consists of a single forsterite grain rimmed by an array of sulfides, oxides, and phosphides. We consider a number of possible origins. We can exclude formation by melting of oxide‐bearing chondrules and CAIs formed in enstatite chondrites. The Pesyanoe clast may have formed in a more oxidized region of the aubrite parent body or, more likely, is a foreign clast from a more oxidized parent body. The ALH 84008 clast likely formed by reaction between sulfides and silicates as a result of cooling, oxidation, or de‐sulfidization. This clast appears to be the first oxide‐bearing clast from an aubritic breccia that formed on the aubrite parent body. Identification of additional oxide‐bearing clasts in aubrites could shed light on whether this was a widespread phenomenon and the origin of these enigmatic objects.     

Oxygen isotope characteristics of chondrules from the Yamato‐82094 ungrouped carbonaceous chondrite: Further evidence for common O‐isotope environments sampled among carbonaceous chondrites

High‐precision secondary ion mass spectrometry (SIMS) was employed to investigate oxygen three isotopes of phenocrysts in 35 chondrules from the Yamato (Y) 82094 ungrouped 3.2 carbonaceous chondrite. Twenty‐one of 21 chondrules have multiple homogeneous pyroxene data (?¹⁷O 3SD analytical uncertainty: 0.7‰); 17 of 17 chondrules have multiple homogeneous pyroxene and plagioclase data. Twenty‐one of 25 chondrules have one or more olivine data matching coexisting pyroxene data. Such homogeneous phenocrysts (1) are interpreted to have crystallized from the final chondrule melt, defining host O‐isotope ratios; and (2) suggest efficient O‐isotope exchange between ambient gas and chondrule melt during formation. Host values plot within 0.7‰ of the primitive chondrule mineral (PCM) line. Seventeen chondrules have relict olivine and/or spinel, with some δ¹⁷O and δ¹⁸O values approaching ?40‰, similar to CAI or AOA‐like precursors. Regarding host chondrule data, 22 of 34 have Mg#s of 98.8–99.5 and ?¹⁷O of ?3.9‰ to ?6.1‰, consistent with most Acfer 094, CO, CR, and CV chondrite chondrules, and suggesting a common reduced O‐isotope reservoir devoid of ¹⁶O‐poor H₂O. Six Y‐82094 chondrules have ?¹⁷O near ?2.5‰, with Mg#s of 64–97, consistent with lower Mg# chondrules from Acfer 094, CO, CR, and CV chondrites; their signatures suggest precursors consisting of those forming Mg# ~99, ?¹⁷O: ?5‰ ± 1‰ chondrules plus ¹⁶O‐poor H₂O, at high dust enrichments. Three type II chondrules plot slightly above the PCM line, near the terrestrial fractionation line (?¹⁷O: ~+0.1‰). Their O‐isotopes and olivine chemistry are like LL3 type II chondrules, suggesting they sampled ordinary chondrite‐like chondrule precursors. Finally, three Mg# >99 chondrules have ?¹⁷O of ?6.7‰ to ?8.1‰, potentially due to ¹⁶O‐rich refractory precursor components. The predominance of Mg# ~99, ?¹⁷O: ?5‰ ± 1‰ chondrules and a high chondrule‐to‐matrix ratio suggests bulk Y‐82094 characteristics are closely related to anhydrous dust sampled by most carbonaceous chondrite chondrules.     

First occurrence of pyrophanite (MnTi03) and baddeleyite (ZrO2) in an ordinary chondrite

Abstract A 220 × 430 μm Mg-Al-chromite fragment in the Raguli H3.8 ordinary chondrite exhibits distinct optical and compositional zoning. The dark central region of the Mg-Al-chromite is enriched in MgO, Al₂O₃ and ZnO and depleted in TiO₂, Cr₂O₃, FeO and MnO relative to the lighter outer region. A subhedral olivine grain attached to radiating euhedral ilmenites is present in the central region of the fragment. One of the ilmenite crystals contains a tiny grain (0.5 × 5.8 μm) of baddeleyite (ZrO₂). Two end-member pyrophanite grains (MnTiO₃) occur in the outer portion of the fragment This is the first occurrence of pyrophanite and baddeleyite in an ordinary chondrite. Although it is possible that the Mg-Al-chromite fragment was derived from an achondritic projectile of unusual composition, we offer two alternative models for its formation. These include (a) a multi-stage process involving nebular melting of a chromian-spinel chondrule that had accreted some olivine-bearing, Mn-rich material followed by metamorphism on the parent body, and (b) formation of the fragment on a metamorphosed parent body from an impact melt of a chromite-rich assemblage containing Mn-rich ilmenite. We favor the latter alternative.     

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.     

THE CHEMISTRY AND MINERALOGY OF THE HOMEWOOD,MANITOBA, METEORITE

The Homewood meteorite is a slightly weathered find of 325 grams discovered in 1970 about 64 km southwest of Winnipeg, Manitoba. It consists of olivine (Fa_25.4; 43.8 normative wt. percent), orthopyroxene (Fs_23.3; 28.5 percent), kamacite and taenite (7.5 percent), troilite (5.6 percent), maskelynite (8.3 percent), chromite (1.0 percent), whitlockite (0.7 percent) and minor patchy Ca pyroxene. Bulk chemical analysis yielded Fe_total 21.60 wt. percent, Fe/SiO₂0.55, SiO₂/MgO 1.53 and Fe^O/Fe_total 0.29. Barred olivine, radiating pyroxene and porphyritic chondrules, all with ill-defined outlines, occur in the meteorite. Most chemical and mineralogical features characterize the Homewood meteorite as an L6 (hypersthene) chondrite. The presence of maskelynite, the undulatory extinction, extensive fracturing and pervasive mosaicism of olivine, and the poor definition of chondrule outlines suggest that the Homewood meteorite has been shocked in the range of 300–350 kbar.     

Oxygen isotope systematics of chondrule olivine,pyroxene, and plagioclase in one of the most pristine CV3Red chondrites (Northwest Africa 8613)

We performed in situ oxygen three‐isotope measurements of chondrule olivine, pyroxenes, and plagioclase from the newly described CV_Red chondrite NWA 8613. Additionally, oxygen isotope ratios of plagioclase in chondrules from the Kaba CV3_OxB chondrite were determined to enable comparisons of isotope ratios and degree of alteration of chondrules in both CV lithologies. NWA 8613 was affected by only mild thermal metamorphism. The majority of oxygen isotope ratios of olivine and pyroxenes plot along a slope‐1 line in the oxygen three‐isotope diagram, except for a type II and a remolten barred olivine chondrule. When isotopic relict olivine is excluded, olivine, and low‐ and high‐Ca pyroxenes are indistinguishable regarding Δ¹⁷O values. Conversely, plagioclase in chondrules from NWA 8613 and Kaba plot along mass‐dependent fractionation lines. Oxygen isotopic disequilibrium between phenocrysts and plagioclase was caused probably by exchange of plagioclase with ¹⁶O‐poor fluids on the CV parent body. Based on an existing oxygen isotope mass balance model, possible dust enrichment and ice enhancement factors were estimated. Type I chondrules from NWA 8613 possibly formed at moderately high dust enrichment factors (50× to 150× CI dust relative to solar abundances); estimates for water ice in the chondrule precursors range from 0.2× to 0.6× the nominal amount of ice in dust of CI composition. Findings agree with results from an earlier study on oxygen isotopes in chondrules of the Kaba CV chondrite, providing further evidence for a relatively dry and only moderately high dust‐enriched disk in the CV chondrule‐forming region.     

THE MINERALOGY AND CHEMISTRY OF THE ALTA'AMEEM METEORITE

The Alta'ameem hypersthene chondrite is a light gray brecciated and metamorphosed meteorite composed mainly of olivine (27% Fa), orthopyroxene (24.5% Fs) and plagioclase (An¹⁰). Other minerals include troilite, kamacite, taenite, chromite, ilmenite, clinopyroxene, chalcopyrite, and apatite or merrillite. The mineralogical and chemical analyses suggest that the Alta'ameem meteorite belongs to the amphoterite group of chondrites. The chemical composition includes the following: Fe 3.39, Ni 1.13, Co 0.05, Cu 0.01, FeS 6.48, SiO₂ 39.48, TiO₂ 0.28, Al₂O₃ 2.25, FeO 16.46, MnO 0.40, MgO 25.66, CaO 1.47, Na₂O 1.05, K₂O 0.15, P₂O₅ 0.47, Cr₂O₃ 0.45; total 99.18.