The origin of chondrules and chondrites: Debris from low‐velocity impacts between molten planetesimals?

Abstract– We investigate the hypothesis that many chondrules are frozen droplets of spray from impact plumes launched when thin‐shelled, largely molten planetesimals collided at low speed during accretion. This scenario, here dubbed “splashing,” stems from evidence that such planetesimals, intensely heated by ²⁶Al, were abundant in the protoplanetary disk when chondrules were being formed approximately 2 Myr after calcium‐aluminum‐rich inclusions (CAIs), and that chondrites, far from sampling the earliest planetesimals, are made from material that accreted later, when ²⁶Al could no longer induce melting. We show how “splashing” is reconcilable with many features of chondrules, including their ages, chemistry, peak temperatures, abundances, sizes, cooling rates, indented shapes, “relict” grains, igneous rims, and metal blebs, and is also reconcilable with features that challenge the conventional view that chondrules are flash‐melted dust‐clumps, particularly the high concentrations of Na and FeO in chondrules, but also including chondrule diversity, large phenocrysts, macrochondrules, scarcity of dust‐clumps, and heating. We speculate that type I (FeO‐poor) chondrules come from planetesimals that accreted early in the reduced, partially condensed, hot inner nebula, and that type II (FeO‐rich) chondrules come from planetesimals that accreted in a later, or more distal, cool nebular setting where incorporation of water‐ice with high Δ¹⁷O aided oxidation during heating. We propose that multiple collisions and repeated re‐accretion of chondrules and other debris within restricted annular zones gave each chondrite group its distinctive properties, and led to so‐called “complementarity” and metal depletion in chondrites. We suggest that differentiated meteorites are numerically rare compared with chondrites because their initially plentiful molten parent bodies were mostly destroyed during chondrule formation.     

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.     

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.     

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.     

CONSTRAINTS ON CHONDRULE ORIGIN FROM PETROLOGY OF ISOTOPICALLY CHARACTERIZED CHONDRULES IN THE ALLENDE METEORITE

Petrographic and chemical features of Allende ferromagnesian chondrules previously analyzed for oxygen and silicon isotopes by Clayton et al. (1983a) provide additional information on chondrule origin. Allende, like other carbonaceous chondrites, contains two chondrule populations, but one of these is represented by only one chondrule in this isotopically characterized set. All Allende chondrules fall along an isotopic mixing line, probably defined by an ¹⁶O-rich solid component and an isotopically heavier oxygen gaseous exchange component. Differences in the amounts of isotopic exchange for porphyritic and barred chondrules presumably resulted from varying degrees of melting. Those porphyritic chondrules containing abundant relict grains experienced the least isotopic exchange. Chondrules with high bulk FeO/(FeO + MgO) ratios apparently persisted longer as liquids and contain more of the exchange component. The distinct directions of oxygen isotopic exchange in chondrules from carbonaceous, ordinary, and enstatite chondrites indicate that each formed from different solid precursor materials. Silicon isotopic variations in Allende chondrules probably reflect evaporative loss of lighter isotopes; however, silicon loss is also controlled by chondrule sizes, which are unknown. Observed correlations point to the importance of kinetic factors in a gaseous nebula for chondrule genesis, and are not consistent with models that explain chondrules as mixtures of several solids with distinct oxygen and silicon isotopic compositions.     

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.     

Free collisions in a microgravity many-particle experiment – II: The collision dynamics of dust-coated chondrules

The formation of planetesimals in the early Solar System is hardly understood, and in particular the growth of dust aggregates above millimeter sizes has recently turned out to be a difficult task in our understanding (Zsom, A., Ormel, C.W., Güttler, C., Blum, J., Dullemond, C.P. [2010]. Astron. Astrophys., 513, A57). Laboratory experiments have shown that dust aggregates of these sizes stick to one another only at unreasonably low velocities. However, in the protoplanetary disk, millimeter-sized particles are known to have been ubiquitous. One can find relics of them in the form of solid chondrules as the main constituent of chondrites. Most of these chondrules were found to feature a fine-grained rim, which is hypothesized to have formed from accreting dust grains in the solar nebula. To study the influence of these dust-coated chondrules on the formation of chondrites and possibly planetesimals, we conducted collision experiments between millimeter-sized, dust-coated chondrule analogs at velocities of a few cm s^?1. For 2 and 3 mm diameter chondrule analogs covered by dusty rims of a volume filling factor of 0.18 and 0.35–0.58, we found sticking velocities of a few cm s^?1. This velocity is higher than the sticking velocity of dust aggregates of the same size. We therefore conclude that chondrules may be an important step towards a deeper understanding of the collisional growth of larger bodies. Moreover, we analyzed the collision behavior in an ensemble of dust aggregates and non-coated chondrule analogs. While neither the dust aggregates nor the solid chondrule analogs show sticking in collisions among their species, we found an enhanced sicking efficiency in collisions between the two constituents, which leads us to the conjecture that chondrules might act as “catalyzers” for the growth of larger bodies in the young Solar System.     

Oxygen isotope and chemical compositions of magnetite and olivine in the anomalous CK3 Watson 002 and ungrouped Asuka‐881595 carbonaceous chondrites: Effects of parent body metamorphism

We report in situ O isotope and chemical compositions of magnetite and olivine in chondrules of the carbonaceous chondrites Watson‐002 (anomalous CK3) and Asuka (A)‐881595 (ungrouped C3). Magnetite in Watson‐002 occurs as inclusion‐free subhedral grains and rounded inclusion‐bearing porous grains replacing Fe,Ni‐metal. In A‐881595, magnetite is almost entirely inclusion‐free and coexists with Ni‐rich sulfide and less abundant Ni‐poor metal. Oxygen isotope compositions of chondrule olivine in both meteorites plot along carbonaceous chondrite anhydrous mineral (CCAM) line with a slope of approximately 1 and show a range of Δ¹⁷O values (from approximately ?3 to ?6‰). One chondrule from each sample was found to contain O isotopically heterogeneous olivine, probably relict grains. Oxygen isotope compositions of magnetite in A‐881595 plot along a mass‐dependent fractionation line with a slope of 0.5 and show a range of Δ¹⁷O values from ?2.4‰ to ?1.1‰. Oxygen isotope compositions of magnetite in Watson‐002 cluster near the CCAM line and a Δ¹⁷O value of ?4.0‰ to ?2.9‰. These observations indicate that magnetite and chondrule olivine are in O isotope disequilibrium, and, therefore, not cogenetic. We infer that magnetite in CK chondrites formed by the oxidation of pre‐existing metal grains by an aqueous fluid during parent body alteration, in agreement with previous studies. The differences in Δ¹⁷O values of magnetite between Watson‐002 and A‐881595 can be attributed to their different thermal histories: the former experienced a higher degree of thermal metamorphism that led to the O isotope exchange between magnetite and adjacent silicates.     

Chondrules: Precursors and interactions with the nebular gas

Abstract– Chondrule compositions suggest either ferroan precursors and evaporation, or magnesian precursors and condensation. Type I chondrule precursors include granoblastic olivine aggregates (planetary or nebular) and fine‐grained (dustball) precursors. In carbonaceous chondrites, type I chondrule precursors were S‐free, while type II chondrules have higher Fe/Mn than in ordinary chondrites. Many type II chondrules contain diverse forsteritic relicts, consistent with polymict dustball precursors. The relationship between finer and coarser grained type I chondrules in ordinary chondrites suggests more evaporation from more highly melted chondrules. Fe metal in type I, and Na and S in type II chondrules indicate high partial pressures in ambient gas, as they are rapidly evaporated at canonical conditions. The occurrence of metal, sulfide, or low‐Ca pyroxene on chondrule rims suggests (re)condensation. In Semarkona type II chondrules, Na‐rich olivine cores, Na‐poor melt inclusions, and Na‐rich mesostases suggest evaporation followed by recondensation. Type II chondrules have correlated FeO and MnO, consistent with condensation onto forsteritic precursors, but with different ratios in carbonaceous chondrites and ordinary chondrites, indicating different redox history. The high partial pressures of lithophile elements require large dense clouds, either clumps in the protoplanetary disk, impact plumes, or bow shocks around protoplanets. In ordinary chondrites, clusters of type I and type II chondrules indicate high number densities and their similar oxygen isotopic compositions suggest recycling together. In carbonaceous chondrites, the much less abundant type II chondrules were probably added late to batches of type I chondrules from different O isotopic reservoirs.     

Chemistry and oxygen isotopic composition of cluster chondrite clasts and their components in LL3 chondrites

Cluster chondrites are characterized by close‐fit textures of deformed and indented chondrules, taken as evidence for hot chondrule accretion (Metzler 2012 ). We investigated seven cluster chondrite clasts from six brecciated LL3 chondrites and measured their bulk oxygen isotopic and chemical composition, including REE, Zr, and Hf. The same parameters were measured in situ on 93 chondrules and 4 interchondrule matrix areas. The CI‐normalized REE patterns of the clasts are flat, showing LL‐chondritic concentrations. The mean chemical compositions of chondrules in clasts and other LL chondrites are indistinguishable and we conclude that cluster chondrite chondrules are representative of the normal LL chondrule population. Type II chondrules are depleted in MgO, Al₂O₃ and refractory lithophiles (REE, Zr, Hf) by factors between 0.65 and 0.79 compared to type I chondrules. The chondrule REE patterns are basically flat with slight LREE < HREE fractionations. Many chondrules exhibit negative Eu anomalies while matrix shows a complementary pattern. Chondrules scatter along a correlation line with a slope of 0.63 in the oxygen 3‐isotope diagram, interpreted as the result of O‐isotope exchange between chondrule melts and ¹⁸O‐rich nebular components. In one clast, a distinct anticorrelation between chondrule size and δ¹⁸O is found, which may indicate a more intense oxygen isotope exchange by smaller chondrules. In some clasts the δ¹⁸O values of type I chondrules are correlated with concentrations of SiO₂ and MnO and anticorrelated with MgO, possibly due to the admixture of a SiO₂‐ and MnO‐rich component to chondrule melts during oxygen isotope exchange. Two chondrules with negative anomalies in Sm, Eu, and Yb were found and may relate their precursors to refractory material known from group III CAIs. Furthermore, three chondrules with strong LREE > HREE and Zr/Hf fractionations were detected, whose formation history remains to be explained.     

Anorthite‐rich chondrules in CR and CH carbonaceous chondrites: Genetic link between calcium‐aluminum‐rich inclusions and ferromagnesian chondrules

Abstract— Anorthite‐rich chondrules in CR and CH carbonaceous chondrites consist of magnesian low‐Ca pyroxene and forsterite phenocrysts, FeNi‐metal nodules, interstitial anorthite, Al‐Ti‐Cr‐rich low‐Ca and high‐Ca pyroxenes, and crystalline mesostasis composed of silica, anorthite and high‐Ca pyroxene. Three anorthite‐rich chondrules contain relic calcium‐aluminum‐rich inclusions (CAIs) composed of anorthite, spinel, ±Al‐diopside, and ± forsterite. A few chondrules contain regions which are texturally and mineralogically similar to magnesian (type I) chondrules and consist of forsterite, low‐Ca pyroxene and abundant FeNi‐metal nodules. Anorthite‐rich chondrules in CR and CH chondrites are mineralogically similar to those in CV and CO carbonaceous chondrites, but contain no secondary nepheline, sodalite or ferrosilite. Relatively high abundances of moderately‐volatile elements such as Cr, Mn and Si in the anorthite‐rich chondrules suggest that these chondrules could not have been produced by volatilization of the ferromagnesian chondrule precursors or by melting of the refractory materials only. We infer instead that anorthite‐rich chondrules in carbonaceous chondrites formed by melting of the reduced chondrule precursors (olivine, pyroxenes, FeNi‐metal) mixed with the refractory materials, including relic CAIs, composed of anorthite, spinel, high‐Ca pyroxene and forsterite. The observed mineralogical and textural similarities of the anorthite‐rich chondrules in several carbonaceous chondrite groups (CV, CO, CH, CR) may indicate that these chondrules formed in the region(s) intermediate between the regions where CAIs and ferromagnesian chondrules originated. This may explain the relative enrichment of anorthite‐rich chondrules in ¹⁶O compared to typical ferromagnesian chondrules (Russell et al., 2000).     

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.     

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.     

Chondritic ingredients: I. Usual suspects and some oddballs in the Leoville CV3 meteorite

Abstract– Reduced CV3 chondrites are relatively pristine rocks and prime candidates for studies exploring processes that predated planet formation. We closely examined the petrographic features and trace elemental composition of different CV3 constituents in the accretionary breccia Leoville. The petrographic results are presented here. Our sample (2.2 cm²) is not brecciated. The main ingredient—about 65 area%—is fine‐ to coarse‐grained ferromagnesian type I chondrules. Minor constituents (in order of 2‐D abundance) include refractory inclusions, Al‐rich chondrules, and very fine‐crystalline clasts of moderately volatile composition. Type II chondrules and metal nuggets occur sporadically. The chondrule–matrix ratio is approximately 3:1. Medium‐ and coarse‐grained chondrules exhibit porphyritic textures, probably caused by incomplete melting, and frequent, partial or continuous, recrystallized dust rims. The fine‐grained population most likely represents randomly sectioned dust rims. The rim material and some of the medium‐grained objects are relatively troilite‐rich. Iron‐nickel metal is rare. In addition, almost all constituents show strikingly ragged or convoluted outlines. Only a few, rim‐less components exhibit smooth contours. Evidence for incomplete melting and the formation of recrystallized or igneous rims in carbonaceous chondrites is well established, suggesting that both processes were widespread events. The observed features in Leoville support this conclusion. In addition, our findings indicate that surface abrasion in a turbulent dust‐filled regime may have taken place after the consolidation of dust rims. Alternatively, the irregular, convoluted nature of at least the rimmed chondrules may have been inherent to the dust accretion event and was not erased by subsequent heating.     

Noble gases in chondrules and associated metal‐sulfide‐rich samples: Clues on chondrule formation and the behavior of noble gas carrier phases

Abstract— Chondrules are generally believed to have lost most or all of their trapped noble gases during their formation. We tested this assumption by measuring He, Ne, and Ar in chondrules of the carbonaceous chondrites Allende (CV3), Leoville (CV3), Renazzo (CR2), and the ordinary chondrites Semarkona (LL3.0), Bishunpur (LL3.1), and Krymka (LL3.1). Additionally, metalsulfide‐rich chondrule coatings were measured that probably formed from chondrule metal. Low primordial ²⁰Ne concentrations are present in some chondrules, while even most of them contain small amounts of primordial ³⁶Ar. Our preferred interpretation is that‐in contrast to CAIs‐the heating of the chondrule precursor during chondrule formation was not intense enough to expel primordial noble gases quantitatively. Those chondrules containing both primordial ²⁰Ne and ³⁶Ar show low presolar‐diamond‐like ³⁶Ar/²⁰Ne ratios. In contrast, the metal‐sulfide‐rich coatings generally show higher gas concentrations and Q‐like ³⁶Ar/²⁰Ne ratios. We propose that during metalsilicate fractionation in the course of chondrule formation, the Ar‐carrying phase Q became enriched in the metal‐sulfide‐rich chondrule coatings. In the silicate chondrule interior, only the most stable Ne‐carrying presolar diamonds survived the melting event leading to the low observed ³⁶Ar/²⁰Ne ratios. The chondrules studied here do not show evidence for substantial amounts of fractionated solar‐type noble gases from a strong solar wind irradiation of the chondrule precursor material as postulated by others for the chondrules of an enstatite chondrite.     

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.     

Ion microprobe analyses of oxygen three‐isotope ratios of chondrules from the Sayh al Uhaymir 290 CH chondrite using a multiple‐hole disk

Abstract– The ion microprobe is the only technique capable of determining high‐precision stable isotope ratios in individual tiny extraterrestrial particles (≤100 μm in diameter), but these small samples present special analytical challenges. We produced a new sample holder disk with multiple holes (three holes and seven holes), in which epoxy disks containing a single unknown sample and a standard grain are cast and polished. Performance tests for oxygen two‐isotope analyses using San Carlos olivine standard grains show that the new multiple‐hole disks allow accurate analysis of tiny particles if the particles are located within the 500 μm and 1 mm radius of the center of holes for seven‐hole and three‐hole disks, respectively. Using the new seven‐hole disk, oxygen three‐isotope ratios of eight magnesian cryptocrystalline chondrules (approximately 100 μm in diameter) from the Sayh al Uhaymir (SaU) 290 CH chondrite were analyzed by ion microprobe at the University of Wisconsin. Five out of eight chondrules have nearly identical oxygen isotope ratios (Δ¹⁷O = ?2.2 ± 0.6‰; 2SD), which is consistent with those of magnesian cryptocrystalline chondrules in CH/CB and CB chondrites, suggesting a genetic relationship, i.e., formation by a common (possibly impact) heating event. The other three chondrules have distinct oxygen isotope ratios (Δ¹⁷O values from ?6.4‰ to +2.2‰). Given that similar variation in Δ¹⁷O values was observed in type I porphyritic chondrules in a CH/CB chondrite, the three chondrules may have formed in the solar nebula, similar to the type I porphyritic chondrules.     

Refractory calcium‐aluminum‐rich inclusions and aluminum‐diopside‐rich chondrules in the metal‐rich chondrites Hammadah al Hamra 237 and Queen Alexandra Range 94411

Abstract— The metal‐rich chondrites Hammadah al Hamra (HH) 237 and Queen Alexandra Range (QUE) 94411, paired with QUE 94627, contain relatively rare (<1 vol%) calcium‐aluminum‐rich inclusions (CAIs) and Al‐diopside‐rich chondrules. Forty CAIs and CAI fragments and seven Al‐diopside‐rich chondrules were identified in HH 237 and QUE 94411/94627. The CAIs, ～50–400 μm in apparent diameter, include (a) 22 (56%) pyroxene‐spinel ± melilite (+forsterite rim), (b) 11 (28%) forsterite‐bearing, pyroxene‐spinel ± melilite ± anorthite (+forsterite rim) (c) 2 (5%) grossite‐rich (+spinel‐melilite‐pyroxene rim), (d) 2 (5%) hibonite‐melilite (+spinel‐pyroxene ± forsterite rim), (e) 1 (2%) hibonite‐bearing, spinel‐perovskite (+melilite‐pyroxene rim), (f) 1 (2%) spinel‐melilite‐pyroxene‐anorthite, and (g) 1 (2%) amoeboid olivine aggregate. Each type of CAI is known to exist in other chondrite groups, but the high abundance of pyroxene‐spinel ± melilite CAIs with igneous textures and surrounded by a forsterite rim are unique features of HH 237 and QUE 94411/94627. Additionally, oxygen isotopes consistently show relatively heavy compositions with Δ¹⁷O ranging from ?6%0 to ?10%0 (1σ = 1.3%0) for all analyzed CAI minerals (grossite, hibonite, melilite, pyroxene, spinel). This suggests that the CAIs formed in a reservoir isotopically distinct from the reservoir(s) where “normal”, ¹⁶O‐rich (Δ¹⁷O < ?20%0) CAIs in most other chondritic meteorites formed. The Al‐diopside‐rich chondrules, which have previously been observed in CH chondrites and the unique carbonaceous chondrite Adelaide, contain Al‐diopside grains enclosing oriented inclusions of forsterite, and interstitial anorthitic mesostasis and Al‐rich, Ca‐poor pyroxene, occasionally enclosing spinel and forsterite. These chondrules are mineralogically similar to the Al‐rich barred‐olivine chondrules in HH 237 and QUE 94411/94627, but have lower Cr concentrations than the latter, indicating that they may have formed during the same chondrule‐forming event, but at slightly different ambient nebular temperatures. Aluminum‐diopside grains from two Al‐diopside‐rich chondrules have O‐isotopic compositions (Δ¹⁷O ? ?7 ± 1.1 %0) similar to CAI minerals, suggesting that they formed from an isotopically similar reservoir. The oxygen‐isotopic composition of one Ca, Al‐poor cryptocrystalline chondrule in QUE 94411/94627 was analyzed and found to have Δ¹⁷O ? ?3 ± 1.4%0. The characteristics of the CAIs in HH 237 and QUE 94411/94627 are inconsistent with an impact origin of these metal‐rich meteorites. Instead they suggest that the components in CB chondrites are pristine products of large‐scale, high‐temperature processes in the solar nebula and should be considered bona fide chondrites.     

Maribo—A new CM fall from Denmark

Abstract– Maribo is a new Danish CM chondrite, which fell on January 17, 2009, at 19:08:28 CET. The fall was observed by many eye witnesses and recorded by a surveillance camera, an all sky camera, a few seismic stations, and by meteor radar observatories in Germany. A single fragment of Maribo with a dry weight of 25.8 g was found on March 4, 2009. The coarse‐grained components in Maribo include chondrules, fine‐grained olivine aggregates, large isolated lithic clasts, metals, and mineral fragments (often olivine), and rare Ca,Al‐rich inclusions. The components are typically rimmed by fine‐grained dust mantles. The matrix includes abundant dust rimmed fragments of tochilinite with a layered, fishbone‐like texture, tochilinite–cronstedtite intergrowths, sulfides, metals, and carbonates often intergrown with tochilinite. The oxygen isotopic composition: (δ¹⁷O = ?1.27‰; δ¹⁸O = 4.96‰; Δ¹⁷O = ?3.85‰) plots at the edge of the CM field, close to the CCAM line. The very low Δ¹⁷O and the presence of unaltered components suggest that Maribo is among the least altered CM chondrites. The bulk chemistry of Maribo is typical of CM chondrites. Trapped noble gases are similar in abundance and isotopic composition to other CM chondrites, stepwise heating data indicating the presence of gas components hosted by presolar diamond and silicon carbide. The organics in Maribo include components also seen in Murchison as well as nitrogen‐rich components unique to Maribo.     

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.