RELATIVE ABUNDANCES OF CHONDRULE PRIMARY TEXTURAL TYPES IN ORDINARY CHONDRITES AND THEIR BEARING ON CONDITIONS OF CHONDRULE FORMATION

A petrographic survey of > 1600 chondrules in thin-sections of 12 different mildly to highly unequilibrated H-, L-, and LL-chondrites, as well as morphological and textural study of 141 whole chondrules separated from 11 of the same chondrites, was used to determine the relative abundances of definable chondrule primary textural types. Percentage abundances of various chondrule types are remarkably similar in all chondrites studied and are ～ 47–52 porphyritic olivine-pyroxene (POP), 15–27 porphyritic olivine (PO), 9–11 porphyritic pyroxene (PP), 3–4 barred olivine (BO), 7–9 radial pyroxene (RP), 2–5 granular olivine-pyroxene (GOP), 3–5 cryptocrystalline (C), and ≤ 1 metallic (M). Neither chondrule size nor shape is strongly correlated with textural type. Compound and cratered chondrules, which are interpreted as products of collisions between plastic chondrules, comprise ～ 2–28% of nonporphyritic (RP, GOP, C) but only ～ 2–9% of porphyritic (POP, PO, PP, BO) chondrules, leading to a model-dependent implication that nonporphyritic chondrules evolved at number densities (chondrules per unit volume of space) which were 10² to 10⁴ times greater than those which prevailed during porphyritic chondrule formation (total range of ～ 1 to ～ 10⁶ m^?3). Distinctive “rims” of fine-grained sulfides and/or silicates occur on both porphyritic and nonporphyritic types and appear to post-date chondrule formation. Apparently, either the same process(es) contributed chondrules to all unequilibrated ordinary chondrites or, if genetically different, the various chondrule types were well mixed before incorporation into chondrites. Melting of pre-existing materials is the mechanism favored for chondrule formation.     

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.     

Magnesium isotopic fractionations in barred olivine chondrules from the Allende meteorite

Abstract— The Mg‐isotopic compositions in five barred olivine (BO) chondrules, one coarse‐grained rim of a BO chondrule, a relic spinel in a BO chondrule, one skeletal olivine chondrule similar to BO chondrules in mineralogy and composition, and two non‐BO chondrules from the Allende meteorite have been measured by thermal ionization mass spectrometry. The Mg isotopes are not fractionated and are within terrestrial standard values (±2.0%o per amu) in seven of the eight analyzed ferromagnesian chondrules. A clump of relic spinel grain and its host BO chondrule R‐11 give well‐resolvable Mg fractionations that show an enrichment of the heavier isotopes, up to +2.5%‰ per amu. The Mg‐isotopic compositions of coarse‐grained rim are identical to those of the host chondrule with BO texture. The results imply that ferromagnesian and refractory precursor components of the Allende chondrule may have been formed from isotopically heterogeneous reservoirs. In the nebula region where Allende chondrules formed, recycling of chondrules and multiple high‐temperature heating did not significantly alter the chemical and isotopic memory of earlier generations. Chemical and isotopic characteristics of refractory precursors of carbonaceous chondrite chondrules and CAIs are more closely related than previously thought. One of the refractory chondrule precursors of CV Allende is enriched in the heavier Mg isotopes and different from those of more common ferromagnesian chondrule precursors. The most probable scenario at the location where chondrule R‐11 formed is as follows. Before chondrule formation, several high‐temperature events occurred and then RPMs, refractory oxides, and silicates condensed from the nebular gas in which Mg isotopes were fractionated. Then, this CAI was transported into the chondrule formation region and mixed with more common, ferromagnesian precursors with normal Mg isotopes, and formed the BO chondrule. Because Mg isotope heterogeneity among silicates and spinel are found in some CAIs (Esat and Taylor, 1984), we cannot rule out the possibility that Mg isotopes of a melted portion of the refractory precursor (i.e., outer portion of CAI) are normal or enriched in the light isotope. Magnesium isotopes in the R‐11 host are also enriched in the heavier isotopes, +2.5%o per amu, which suggests that effects of isotopic heterogeneity among silicates and spinel, if they existed, are not considered to be large. It is possible that CAI precursor silicates partially dissolved during the chondrule forming event, contributing Mg to the melt and producing a uniform Mg‐isotopic signature but enriched in the heavier Mg isotopes, +2.5%‰ per amu. Most Mg isotopes in more common ferromagnesian chondrules represent normal chondritic material. Chemical and Mg‐isotopic signatures formed during nebular fractionations were not destroyed during thermal processes that formed the chondrule, and these were partly preserved in relic phases. Recycling of Allende chondrules and multiple heating at high temperature did not significantly alter the chemical and Mg‐isotopic memory of earlier generations.     

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.     

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

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

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.     

An unusual compound object in Yamato 793408 (H3.2‐an): The missing link between compound chondrules and macrochondrules?

We found a large (~2 mm) compound object in the primitive Yamato 793408 (H3.2‐an) chondrite. It consists mostly of microcrystalline material, similar to chondrule mesostasis, that hosts an intact barred olivine (BO) chondrule. The object contains euhedral pyroxene and large individual olivine grains. Some olivine cores are indicative of refractory forsterites with very low Fe‐ and high Ca, Al‐concentrations, although no ¹⁶O enrichment. The entire object is most likely a new and unique type, as no similar compound object has been described so far. We propose that it represents an intermediate stage between compound chondrules and macrochondrules, and formed from the collision between chondrules at low velocities (below 1 m s^?1) at high temperatures (around 1550 °C). The macrochondrule also trapped and preserved a smaller BO chondrule. This object appears to be the first direct evidence for a genetic link between compound chondrules and macrochondrules. In accordance with previous suggestions and studies, compound chondrules and macrochondrules likely formed by the same mechanism of chondrule collisions, and each represents different formation conditions, such as ambient temperature and collision speed.     

The Allende multicompound chondrule (ACC)—Chondrule formation in a local super‐dense region of the early solar system

In Allende, a very complex compound chondrule (Allende compound chondrule; ACC) was found consisting of at least 16 subchondrules (14 siblings and 2 independents). Its overall texture can roughly be described as a barred olivine object (BO). The BO texture is similar in all siblings, but does not exist in the two independents, which appear as relatively compact olivine‐rich units. Because of secondary alteration of pristine Allende components and the ACC in particular, only limited predictions can be made concerning the original compositions of the colliding melt droplets. Based on textural and mineralogical characteristics, the siblings must have been formed on a very short time scale in a dense, local environment. This is also supported by oxygen isotope systematics showing similar compositions for all 16 subchondrules. Furthermore, the ACC subchondrules are isotopically distinct from typical Allende chondrules, indicating formation in or reaction with a more ¹⁶O‐poor reservoir. We modeled constraints on the particle density required at the ACC formation location, using textural, mineral‐chemical, and isotopic observations on this multicompound chondrule to define melt droplet collision conditions. In this context, we discuss the possible relationship between the formation of complex chondrules and the formation of macrochondrules and cluster chondrites. While macrochondrules may have formed under similar or related conditions as complex chondrules, cluster chondrites certainly require different formation conditions. Cluster chondrites represent a mixture of viscously deformed, seemingly young chondrules of different chemical and textural types and a population of older chondrules. Concerning the formation of ACC calculations suggest the existence of very local, kilometer‐sized, and super‐dense chondrule‐forming regions with extremely high solid‐to‐gas mass ratios of 1000 or more.     

Alkali (Rb/K) abundances in Allende barred-olivine chondrules: Implications for the melting conditions of chondrules

Abstract— In order to study abundances of alkali metals in chondrules, 25 petrographically characterized chondrules, including 18 barred olivine (BO) chondrules from the Allende (CV3) meteorite, were analyzed for alkalis (K and Rb) and alkaline earths (Sr, Ba, Ca and Mg) by mass spectrometric isotope dilution. Most BO chondrules with higher alkalis (>CI level) have nearly CI-chondritic Rb/K ratios, while those with lower alkalis clearly show higher Rb/K ratios than the CI-chondritic. In general, BO chondrules with higher Rb/K exhibit more depletion of alkalis relative to Ca. The mean olivine Fa for individual chondrules positively correlates with bulk alkali concentrations in BO type but not in porphyritic type chondrules. These observations suggest that some BO chondrules formed from more reducing assemblages of precursor minerals, which experienced more intensive vaporization losses of alkalis, accompanied by Rb/K fractionation, during the chondrule-formation melting.     

The relative formation ages of ferromagnesian chondrules inferred from their initial aluminum‐26/aluminum‐27 ratios

Abstract— We performed a systematic high‐precision secondary ion mass spectrometry ²⁶Al‐²⁶Mg isotopic study for 11 ferromagnesian chondrules from the highly unequilibrated ordinary chondrite Bishunpur (LL3.1). The chondrules are porphyritic and contain various amounts of olivine and pyroxene and interstitial plagioclase and/or glass. The chemical compositions of the chondrules vary from FeO‐poor to FeO‐rich. Eight chondrules show resolvable ²⁶Mg excesses with a maximum δ²⁶Mg of ?1% in two chondrules. The initial ²⁶Al/²⁷Al ratios inferred for these chondrules range between (2.28 ± 0.73) × 10^?5 to (0.45 ± 0.21) × 10^?5. Assuming a homogeneous distribution of Al isotopes in the early solar system, this range corresponds to ages relative to CAIs between 0.7 ± 0.2 Ma and 2.4_+0.7^?0.4 Ma. The inferred total span of the chondrule formation ages is at least 1 Ma, which is too long to form chondrules by the X‐wind. The initial ²⁶Al/27Al ratios of the chondrules are found to correlate with the proportion of olivine to pyroxene suggesting that olivine‐rich chondrules formed earlier than pyroxene‐rich chondrules. Though we do not have a completely satisfactory explanation of this correlation we tentatively interpret it as a result of evaporative loss of Si from earlier generations of chondrules followed by addition of Si to the precursors of later generation chondrules.     

Size-frequency distributions of chondrules in CO3 chondrites

Abstract— The size-frequency distributions of chondrules in 11 CO3 chondrites were determined by petrographic analysis of thin sections. CO chondrites have the smallest chondrules of any major chondrite group. In order of decreasing chondrule size, chondrite groups can be arranged as CV ≥ LL > L > H ≥ CM ≥ EH > CO. Chondrule size varies significantly among different CO chondrites; there is a tendency for chondrules to increase in average size with increasing metamorphic grade of the whole-rock. Different chondrule types in CO chondrites have distinct size-frequency distributions: in order of decreasing chondrule size, BO > PO > PP > POP > RP = C. The large size of BO chondrules is problematic; however, PO chondrules are among the largest because ～20% of them contain very coarse relict olivine grains that constitute 40–90 vol.% of the individual chondrules. PP chondrules may be larger than POP chondrules because some of them contain coarse relict pyroxene grains; a compound object consisting of a POP chondrule attached to a large relict pyroxene grain occurs in Lancé. The mean proportions of chondrule types in CO chondrites are estimated to be 69% POP, 18% PP, 8% PO, 2% BO, 2% RP, 1% C and <0.1% GOP. CO chondrites thus contain a smaller proportion of nonporphyritic chondrules than ordinary or EH chondrites, but a larger proportion than CV chondrites. Relative proportions of chondrule types vary with size interval: PO chondrules decrease fairly regularly in abundance with decreasing chondrule size, and RP chondrules appear to be most abundant in the smallest size intervals.     

The oxygen isotope compositions of olivine in main group (MG) pallasites: New measurements by adopting an improved laser fluorination approach

Oxygen isotope measurements of olivine in main group (MG) pallasites by traditional laser fluorination method are associated with some uncertainties including terrestrial weathering, incomplete olivine reaction, and sample state. We improved our laser fluorination approach by pretreating olivine grains with acid to remove terrestrial weathering products and by modifying the sample holder for an efficient and complete laser reaction. Our experiments on Brahin olivine demonstrate that acid-washing successfully removes the terrestrial weathering with <0.1‰ variation in δ¹⁸O value and, at the same time, improving the ∆¹⁷O value significantly. We also achieved a complete olivine fluorination by employing a custom-designed sample holder with “V”-shaped profile having rounded bottom because incomplete/partial reaction of olivine gives comparatively lighter δ¹⁸O values. Using these new techniques, we present precise triple oxygen isotope data (N = 72) of 25 olivine samples separated from main group pallasites. The data are, on average, ~0.5‰ heavier in δ¹⁸O relative to the values published in the literature for the same samples. Critically, the ∆¹⁷O values of MG pallasites and to some extent their Fo-contents suggest that there are at least two populations of olivine. Based on our improved data set, we propose that MG pallasites potentially have high-∆¹⁷O- and low-∆¹⁷O-bearing subgroups that are statistically distinct. The subgroups present average ∆¹⁷O values of −0.166 ± 0.003 (2SE; N = 16) and −0.220 ± 0.003 (2SE; N = 9), respectively. Furthermore, the high-∆¹⁷O-bearing subgroup samples trend toward lower Fo-contents compared to the other subgroup. Taken together, our data provide evidence that argues against a single parent body origin for MG pallasites.     

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.     

Temperature conditions for chondrule formation

Abstract— The liquidus temperatures of chondrules range from about 1200 °C to almost 1900 °C, based on the calculation of Herzberg (1979). Dynamic melting and crystallization experiments with no external seeding suggest that some chondrule textures formed with initial temperatures below the liquidus (e.g., porphyritic, granular) and some were completely melted (e.g., excentroradial, glassy). Type I and III chondrules in carbonaceous chondrites in this interpretation consist of incompletely melted magnesian chondrules, completely melted silica-rich chondrules and intermediate composition chondrules with both porphyritic and nonporphyritic textures. A similar pattern for ordinary chondrites, with data also for Type II porphyritic and barred olivine chondrules, suggests that few chondrules with liquidus temperatures over 1750 °C were completely melted and few with under 1400 °C were incompletely melted. The range of liquidus temperatures for barred olivine chondrules, for which initial temperatures appear to have been essentially at the liquidus, is similar. Most chondrules may therefore have been heated to temperatures of 1400–1750 °C and, because of a peak in the distribution of barred olivine chondrule temperatures at 1500–1550 °C, the temperatures appear normally distributed within this range. Given a narrow range of temperatures, bulk composition is at least as important as initial temperature in controlling chondrule textures. Truly granular (not microporphyritic) Type I and truly glassy Type II and III chondrules appear under-represented in nature according to this model, based on internal nucleation experiments. External heterogeneous nucleation, or seeding due to droplet-dust collisions, is likely to occur in a dusty nebula and has been shown to reproduce chondrule textures experimentally. Generally high initial temperatures (1600–1800 °C), coupled with dust-seeding of superheated droplets of less refractory composition is an alternative explanation of chondrule textures. Cooling rates of 100–1000 °C/hr are required for chondrules, which must have been mass produced in clouds with sufficient particle density to buffer cooling rate and perhaps also initial temperature. Melting precursor particles in a thick clump and/or the nebular mid-plane would provide evaporation and thus explain the high oxidation state and volatile content of chondrules, relative to the bulk hydrogen-rich nebula, as well as the nature of the cooling.     

NWA 1152 and Sahara 00182: New primitive carbonaceous chondrites with affinities to the CR and CV groups

Abstract— We have investigated the mineralogy, petrography, bulk chemistry, and light element isotope composition of the ungrouped chondrites North West Africa (NWA) 1152 and Sahara 00182. NWA 1152 contains predominantly type 1 porphyritic olivine (PO) and porphyritic olivinepyroxene (POP) chondrules. Chondrule silicates are magnesium‐rich (Fo_{98.8 ± 1.2}, n = 36; Fs_{2.3 ± 2.1} Wo_{1.2 ± 0.3}, n = 23). Matrix comprises ?40 vol% of the sample and is composed of a micron sized silicate groundmass with larger silicate, sulfide, magnetite, and Fe‐Ni metal (Ni ?50 wt%) grains. Phyllosilicates were not observed in the matrix. Refractory inclusions are rare (0.3 vol%) and are spinel pyroxene aggregates or amoeboid olivine aggregates; melilite is absent from the refractory inclusions. Sahara 00182 contains predominantly type 1 PO chondrules, POP chondrules are less common. Most chondrules contain blebs of, and are often rimmed with, Fe‐Ni metal and sulfide. Chondrule phenocrysts are magnesium‐rich (Fo_{92.2 ± 0.6}, n = 129; Fs_{4.4 ± 1.8} Wo_{1.3 ± 1.1}, n = 16). Matrix comprises ?30 vol% of the meteorite and is predominantly sub‐micron silicates, with rare larger silicate gains. Matrix Fe‐Ni metal (mean Ni = 5.8 wt%) and sulfide grains are up to mm scale. No phyllosilicates were observed in the matrix. Refractory inclusions are rare (1.1 vol%) and melilite is absent. The oxygen isotope composition of NWA 1152 falls within the range of the CV chondrites with δ¹⁷O = ?3.43%0 δ¹⁸O = 0.70%0 and is similar to Sahara 00182, δ¹⁷O = ?3.89%0, δ¹⁸O = ?0.19%0 (Grossman and Zipfel 2001). Based on mineralogical and petrographic characteristics, we suggest NWA 1152 and Sahara 00182 show many similarities with the CR chondrites, however, oxygen isotopes suggest affinity with the CVs. Thus, neither sample can be assigned to any of the currently known carbonaceous chondrite groups based on traditionally recognized characteristics. Both samples demonstrate the complexity of inter‐ and intra‐group relationships of the carbonaceous chondrites. Whatever their classification, N WA 1152 and Sahara 00182 represent a source of relatively pristine solar system material.     

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

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

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.     

Origin of isolated olivine grains in carbonaceous chondrites

We report microscopic, cathodoluminescence, chemical, and O isotopic measurements of FeO‐poor isolated olivine grains (IOG) in the carbonaceous chondrites Allende (CV3), Northwest Africa 5958 (C2‐ung), Northwest Africa 11086 (CM2‐an), and Allan Hills 77307 (CO3.0). The general petrographic, chemical, and isotopic similarity with bona fide type I chondrules confirms that the IOG derived from them. The concentric CL zoning, reflecting a decrease in refractory elements toward the margins, and frequent rimming by enstatite are taken as evidence of interaction of the IOG with the gas as stand‐alone objects. This indicates that they were splashed out of chondrules when these were still partially molten. CaO‐rich refractory forsterites, which are restricted to ?¹⁷O <?4‰ likely escaped equilibration at lower temperatures because of their large size and possibly quicker quenching. The IOG thus bear witness to frequent collisions in the chondrule‐forming regions.