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1.
The magnesium isotopic compositions of 26 hibonite-bearing inclusions from the CM chondrite Murchison, as well as isotopic measurements on a subset of these samples for oxygen, titanium, and lithium-beryllium-boron are reported along with oxygen isotopic data for an additional 13 hibonites that were previously investigated for other isotope systems (magnesium, potassium, calcium, and titanium) and rare earth element concentrations. Magnesium isotopic compositions divide CM hibonites into two distinct populations which correlate perfectly with their mineralogy and morphology, as previously discovered by Ireland [Ireland T. R. (1988) Correlated morphological, chemical, and isotopic characteristics of hibonites from the Murchison carbonaceous chondrite. Geochim. Cosmochim. Acta52, 2827-2839]: Spinel-HIBonite spherules (SHIBs) bear evidence of in situ26Al decay, whereas PLAty-Crystals (PLACs) and Blue AGgregates (BAGs) either lack resolvable 26Mg-excesses or exhibit 26Mg deficits by up to ∼4‰. High precision, multiple collector SIMS analyses show that 6 of 7 SHIBs investigated fall on a single correlation line implying 26Al/27Al = (4.5 ± 0.2) × 10−5 at the time of isotopic closure, consistent with the “canonical” 26Al abundance characteristic of internal isochrons in many calcium-aluminum-rich inclusions (CAIs). One SHIB sample exhibits Δ26Mg∗ consistent with a “supracanonical” 26Al/27Al ratio of (6.4 ± 0.5) × 10−5. The PLAC hibonites contain highly anomalous titanium isotopic compositions, with δ50Ti values ranging from −80‰ to almost +200‰, whereas SHIBs generally lack large Ti isotopic anomalies.Eight out of 11 26Al-free PLAC hibonite grains record 10B/11B excesses that correlate with Be/B; the inferred initial 10Be/9Be ratio of (5.1 ± 1.4) × 10−4 is lower than the best-constrained 10Be/9Be of (8.8 ± 0.6) × 10−4 in a CV CAI. The data demonstrate that 10Be cannot be used as a relative chronometer for these objects and that most of the 10Be observed in CAIs must be produced by irradiation of precursor solids in the early solar system. The lack of 26Al in PLAC hibonites indicates that significant amounts of 26Al were not formed in the same spallogenic processes that made 10Be in PLAC precursors. This is most easily understood as indicating very early formation of the PLAC hibonites, prior to the incorporation and mixing of 26Al into the solar nebula, although an alternative scenario, which invokes irradiation under different solar flare conditions, cannot be ruled out. Lithium isotopes are normal within uncertainties, probably reflecting contamination and/or postcrystallization exchange.The oxygen isotopic compositions of SHIBs and PLACs are all highly 16O-enriched, but are not derived from a homogeneous reservoir: Δ17O values span a range of ∼−28‰ to −15‰. The ranges of 16O-enrichment in SHIBs and PLACs overlap and are less “anomalous” than the most 16O-enriched compositions found in meteorites [Kobayashi S., Imai H. and Yurimoto H. (2003) New extreme 16O-rich chondrule in the early solar system. Geochem. J.37, 663-669]. Both PLACs and SHIBs formed in 16O-enriched reservoirs characterized by small-scale heterogeneities in the gas phase. If such heterogeneities were generated by an admixture of relatively 16O-poor gas created by self-shielding during CO photolysis and transported to the hot inner regions of the accretion disk, then this process must have been initiated very early on, prior to the arrival of fresh radioactivity into the inner solar system. Oxygen isotope heterogeneities persisted throughout the formation interval of PLACs, CAI precursors, and SHIBs which could be as long as 3 × 105 years based on 26Al records.One SHIB and one BAG exhibit mass fractionated oxygen isotopic compositions similar to those seen in FUN inclusions and in several platy hibonite crystals [Lee T., Mayeda T. K. and Clayton R. N. (1980) Oxygen isotopic anomalies in Allende inclusion HAL. Geophys. Res. Lett.7, 493-496; Ireland T. R., Zinner E. K., Fahey A. J. and Esat T. M. (1992) Evidence for distillation in the formation of HAL and related hibonite inclusions. Geochim. Cosmochim. Acta56, 2503-2520; Ushikubo T., Hiyagon H. and Sugiura N. (2007) A FUN-like hibonite inclusion with a large 26Mg-excess. Earth Planet. Sci. Lett.254, 115-126]. The suite of mass-fractionated hibonites exhibit a range of isotopic properties, including 26Al/27Al ratios from below detection to a “canonical” level and oxygen and titanium anomalies that are not exceptional by PLAC standards. This suggests that F (fractionation) processes—evaporation under (oxidizing) conditions—are not necessarily associated with sampling a special isotopic reservoir.  相似文献   

2.
The ion microprobe was used to measure Ti and Mg isotopes as well as rare earth and other trace elements in ten hibonites from the CM carbonaceous chondrites Murchison, Murray, and Cold Bokkeveld and in two hibonites and Ti-rich pyroxene from the CV chondrite Allende. In hibonites from Murchison and Murray fission track densities were also measured, as were Th and U concentrations. Eight of the hibonites, from all four meteorites, exhibit large Ti isotopic anomalies, particularly in 50Ti. Two grains from Murray have 50Ti excesses of ~ 10%. At least four nucleosynthetic components are required to account for all the Ti isotopic data. Neutron-rich nuclear statistical equilibrium nucleosynthesis is the most likely process to account for a 50Ti-rich component (with 50Ti49Ti$̆20). The ion probe Ti isotopic measurements confirm that the solar nebula was isotopically heterogeneous on a small spatial scale and argue for a chemical memory origin of the Ti isotopic anomalies which were probably carried into the solar system in the form of refractory dust grains. However, there is no experimental evidence that such interstellar grains survived the formation of the hibonites. The REE and trace element patterns of the hibonites are similar to those seen in CAIs and can be interpreted in terms of fractionation effects during condensation from a gas of solar composition, thus arguing for a solar system origin of the hibonites. Additional evidence for such an origin is provided by the PuTh ratios, which are ~ 10−4, and by the Mg isotopic compositions which are normal except for 26Mg1 due to 26Al.Only three out of ten hibonites exhibit 26Mg1, consistent with previous studies which demonstrated the paucity of 26Mg1 in hibonites. Because of the refractory nature of hibonite and the presence of large Ti isotopic effects, we conclude that a heterogeneous distribution of 26Al in the early solar system is the most likely reason. In particular, our observations of δ50Ti = 15%. and of an isochron with (26Al27Al)0 = 5 × 10−8 in the FUN inclusion HAL are evidence against both late formation and Mg redistribution to explain the lack of 26Al in hibonites.There are no obvious correlations between the Ti isotopic compositions, the presence of 26Mg1, the presence of 244Pu, and the REE and trace element patterns in individual hibonites. This indicates that the anomalous 50Ti, as well as 26A1 and 244Pu, were not co-produced in a single astrophysical source, and/or that these nuclides were introduced into the solar nebula by different carriers before being incorporated into the hibonites.  相似文献   

3.
Low molecular weight monocarboxylic acids are the most abundant water soluble organic compounds in the Murchison and many other CM type carbonaceous chondrites. In this study, we examined the monocarboxylic acids in Murchison and EET96029.20 carbonaceous meteorites using a new sample preparation and introduction technique for gas chromatograph recently developed for volatile, water-soluble organic compounds: solid phase micro-extraction (SPME). We identified more than 50 monocarboxylic acids from Murchison compared with the 18 compounds reported previously. Formic acid, a known interstellar molecule, has been fully analyzed in these carbonaceous meteorites, with its δD value suggesting an interstellar origin. We determined both carbon and hydrogen isotopic ratios of individual monocarboxylic acids in Murchison, to better define the origins and genetic relationships of these compounds. The compound-specific isotopic data reveal a large enrichment in 13C (δ13C up to + 32.5‰) and particularly D (δD up to + 2024‰). The branched acids are substantially enriched in both 13C and D relative to the straight chain acids, with those branched acids containing a quaternary carbon showing the greatest isotopic enrichment. The isotopic difference may be attributed to variations in the different synthetic regimes or terrestrial input of straight chain acids.  相似文献   

4.
The oxygen-isotope compositions (obtained by laser fluorination) of hand-picked separates of isolated forsterite, isolated olivine and chondrules from the Tagish Lake carbonaceous chondrite describe a line (δ17O = 0.95 * δ18O − 3.24; R2 = 0.99) similar to the trend known for chondrules from other carbonaceous chondrites. The isolated forsterite grains (Fo99.6-99.8; δ18O = −7.2‰ to −5.5‰; δ17O = −9.6‰ to −8.2‰) are more 16O-rich than the isolated olivine grains (Fo39.6-86.8; δ18O = 3.1‰ to 5.1‰; δ17O = −0.3‰ to 2.2‰), and have chemical and isotopic characteristics typical of refractory forsterite. Chondrules contain olivine (Fo97.2-99.8) with oxygen-isotope compositions (δ18O = −5.2‰ to 5.9‰; δ17O = −8.1‰ to 1.2‰) that overlap those of isolated forsterite and isolated olivine. An inverse relationship exists between the Δ17O values and Fo contents of Tagish Lake isolated forsterite and chondrules; the chondrules likely underwent greater exchange with 16O-poor nebular gases than the forsterite. The oxygen-isotope compositions of the isolated olivine grains describe a trend with a steeper slope (1.1 ± 0.1, R2 = 0.94) than the carbonaceous chondrite anhydrous mineral line (CCAMslope = 0.95). The isolated olivine may have crystallized from an evolving melt that exchanged with 16O-poor gases of somewhat different composition than those which affected the chondrules and isolated forsterite. The primordial components of the Tagish Lake meteorite formed under conditions similar to other carbonaceous chondrite meteorite groups, especially CMs. Its alteration history has its closest affinities to CI carbonaceous chondrites.  相似文献   

5.
It has been recently suggested that (1) CH chondrites and the CBb/CH-like chondrite Isheyevo contain two populations of chondrules formed by different processes: (i) magnesian non-porphyritic (cryptocrystalline and barred) chondrules, which are similar to those in the CB chondrites and formed in an impact-generated plume of melt and gas resulted from large-scale asteroidal collision, and (ii) porphyritic chondrules formed by melting of solid precursors in the solar nebula. (2) Porphyritic chondrules in Isheyevo and CH chondrites are different from porphyritic chondrules in other carbonaceous chondrites ( [Krot et al., 2005], [Krot et al., 2008a] and [Krot et al., 2008b]). In order to test these hypotheses, we measured in situ oxygen isotopic compositions of porphyritic (magnesian, Type I and ferroan, Type II) and non-porphyritic (magnesian and ferroan cryptocrystalline) chondrules from Isheyevo and CBb chondrites MAC 02675 and QUE 94627, paired with QUE 94611, using a Cameca ims-1280 ion microprobe.On a three-isotope oxygen diagram (δ17O vs. δ18O), compositions of chondrules measured follow approximately slope-1 line. Data for 19 magnesian cryptocrystalline chondrules from Isheyevo, 24 magnesian cryptocrystalline chondrules and 6 magnesian cryptocrystalline silicate inclusions inside chemically-zoned Fe,Ni-metal condensates from CBb chondrites have nearly identical compositions: Δ17O = −2.2 ± 0.9‰, −2.3 ± 0.6‰ and −2.2 ± 1.0‰ (2σ), respectively. These observations and isotopically light magnesium compositions of cryptocrystalline magnesian chondrules in CBb chondrites (Gounelle et al., 2007) are consistent with their single-stage origin, possibly as gas-melt condensates in an impact-generated plume. In contrast, Δ17O values for 11 Type I and 9 Type II chondrules from Isheyevo range from −5‰ to +4‰ and from −17‰ to +3‰, respectively. In contrast to typical chondrules from carbonaceous chondrites, seven out of 11 Type I chondrules from Isheyevo plot above the terrestrial fractionation line. We conclude that (i) porphyritic chondrules in Isheyevo belong to a unique population of objects, suggesting formation either in a different nebular region or at a different time than chondrules from other carbonaceous chondrites; (ii) Isheyevo, CB and CH chondrites are genetically related meteorites: they contain non-porphyritic chondrules produced during the same highly-energetic event, probably large-scale asteroidal collision; (iii) the differences in mineralogy, petrography, chemical and whole-rock oxygen isotopic compositions between CH and CB chondrites are due to various proportions of the nebular and the impact-produced materials.  相似文献   

6.
We report isotopic ratio measurements of small SiC and Si3N4 grains, with special emphasis on presolar SiC grains of type Z, and new nucleosynthesis models for 26Al/27Al and the Ti isotopic ratios in asymptotic giant branch (AGB) stars. With the NanoSIMS we analyzed 310 SiC grains from Murchison (carbonaceous CM2 chondrite) separate KJB (diameters 0.25-0.45 μm) and 153 SiC grains from KJG (diameters 1.8-3.7 μm), 154 SiC and 23 Si3N4 grains from Indarch (enstatite EH4 chondrite) separate IH6 (diameters 0.25-0.65 μm) for their C and N isotopic compositions, 549 SiC and 142 Si3N4 grains from IH6 for their C and Si isotopic compositions, 13 SiC grains from Murchison and 66 from Indarch for their Al-Mg compositions, and eight SiC grains from Murchison and 10 from Indarch for their Ti isotopic compositions. One of the original objectives of this effort was to compare isotopic analyses with the NanoSIMS with analyses previously obtained with the Cameca IMS 3f ion microprobe. Many of the Si3N4 grains from Indarch have isotopic anomalies but most of these apparently originate from adjacent SiC grains. Only one Si3N4 grain, with 13C and 14N excesses, has a likely AGB origin. The C, N, and Si isotopic data show that the percentage of SiC grains of type Y and Z increase with decreasing grain size (from ∼1% for grains >2 μm to ∼5-7% for grains of 0.5 μm), providing an opportunity for isotopic analyses in these rare grains. Our measurements expand the number of Al-Mg analyses on SiC Z grains from 4 to 23 and the number of Ti analyses on Z grains from 2 to 11. Inferred26Al/27Al ratios of Z grains are in the range found in mainstream and Y grains and do not exceed those predicted by models of AGB nucleosynthesis. Cool bottom processing (CBP) has been invoked to explain the low 12C/13C ratios of Z grains, but this process apparently does not lead to increased 26Al production in the parent stars of these grains. This finding is in contrast to presolar oxide grains where CBP is needed to explain their high 26Al/27Al ratios. The low 46,47,49Ti/48Ti ratios found in Z grains and their correlation with low 29Si/28Si ratios extend the trend seen in mainstream grains and confirm an origin in low-metallicity AGB stars. The relatively large excesses in 30Si and 50Ti in Z grains are predicted by our models to be the result of increased production of these isotopes by neutron-capture nucleosynthesis in low-metallicity AGB stars. However, the predicted excesses in 50Ti (and 49Ti) are much larger than those found. Even lowering the strength of the 13C pocket cannot solve this discrepancy in a consistent way.  相似文献   

7.
Chondritic Mg isotope composition of the Earth   总被引：2，自引：0，他引：2  
The processes of planetary accretion and differentiation have potentially been recorded as variations in the stable isotope ratios of the major elements between planetary objects. However, the magnitude of observed isotopic variations for several elements (Mg, Fe, Si) is at the limit of what current analytical precision and accuracy are able to resolve. Here, we present a comprehensive data set of Mg isotope ratios measured in ocean island and mid-ocean ridge basalts, peridotites and chondrites. The precision and accuracy were verified by isotopic standard addition for two samples, one carbonaceous chondrite (Murchison) and one continental flood basalt (BCR-1). In contrast with some previous studies, our data from terrestrial and chondritic materials have invariant Mg isotope ratios within the uncertainty of the method (0.1‰ for the 26Mg/24Mg ratio, 2SD). Although isotopic variations of less than about 0.1‰ could still be present, the data demonstrate that, at this level of uncertainty, the bulk silicate Earth and chondritic Mg reservoir have a homogeneous δ26Mg = −0.23‰ (26Mg/24Mg ratio of the sample relative to the DSM3 standard set to zero by definition). This implies that neither planetary accretion processes nor partial mantle melting and subsequent shallow-level differentiation have fractionated Mg isotope ratios. These observations imply in particular that the formation of the Earth cannot stem from preferential sorting of chondrite constituents that would have been fractionated in their Mg isotope composition. It also implies that unlike oxygen isotopes, there was no zonation in Mg isotopes in the inner solar system.  相似文献   

8.
A corundum-hibonite inclusion, BB-5, has been found in the Murchison carbonaceous chondrite. This is the first reported occurrence of corundum as a major phase in any refractory inclusion, even though this mineral is predicted by thermodynamic calculations to be the first condensate from a cooling gas of solar composition. Ion microprobe measurements of Mg isotopic compositions yield the unexpected result for such an early condensate that 26Mg excesses are small: δN26Mg = 7.0 ± 1.6%. for hibonite and 5.0 ± 4.8%. for corundum, despite very large 27Al24Mg ratios, 130 and 2.74 × 104, respectively. Within the errors, δN26Mg does not vary over this exceedingly large range of 27Al24Mg ratios. The extreme temperature required to melt this inclusion makes a liquid origin unlikely, except possibly by hypervelocity impact involving refractory bodies. If, instead, BB-5 is a direct gas-solid condensate, textural evidence implies that corundum formed first and later reacted to produce hibonite. In this model, BB-5's uniform enrichment in 26Mg must be a characteristic of the reservoir from which it condensed. Because severe difficulties are encountered in making such a reservoir by prior decay of 26Al, nebular heterogeneity in magnesium isotopic composition is a preferred explanation.  相似文献   

9.
Bulk chemical compositions and oxygen isotopic compositions were analyzed for 48 stony cosmic spherules (melted micrometeorites) collected from the Antarctic ice sheet using electron- and ion-microprobes. No clear correlation was found between their isotopic compositions and textures. The oxygen isotopic compositions showed an extremely wide range from −28‰ to +93‰ in δ18O and from −21‰ to +13‰ in Δ17O. In δ18O-δ17O space, most samples (38 out of 48) plot close to the terrestrial fractionation line, but 7 samples plot along the carbonaceous chondrite anhydrous mineral (CCAM) line. Three samples plot well above the terrestrial fractionation line. One of these has a Δ17O of +13‰, the largest value ever found in solar system materials. One possible precursor for this spherule could be 16O-poor planetary material that is still unknown as a meteorite. The majority of the remaining spherules are thought to be related to carbonaceous chondrites.  相似文献   

10.
Low-density graphite spherules from the Murchison carbonaceous chondrite contain TiC grains and possess excess 28Si and 44Ca (from decay of short-lived 44Ti). These and other isotopic anomalies indicate that such grains formed by condensation from mixtures of ejecta from the interior of a core-collapse supernova with those from the exterior. Using homogenized chemical and isotopic model compositions of the eight main burning zones as end-members, Travaglio et al. (1999) attempted to find mixtures whose isotopic compositions match those observed in the graphite spherules, subject to the condition that the atomic C/O ratio = 1. They were partially successful, but this chemical condition does not guarantee condensation of TiC at a higher temperature than graphite, which is indicated by the spherule textures. In the present work, model compositions of relatively thin layers of ejecta within the main burning zones computed by Rauscher et al. (2002) for Type II supernovae of 15, 21 and 25 M? are used to construct mixtures whose chemical compositions cause equilibrium condensation of TiC at a higher temperature than graphite in an attempt to match the textures and isotopic compositions of the spherules simultaneously. The variation of pressure with temperature and the change in elemental abundances with time due to radioactive decay were taken into account in the condensation calculations. Layers were found within the main Ni, O/Ne, He/C and He/N zones that, when mixed together, simultaneously match the carbon, nitrogen and oxygen isotopic compositions, 44Ti/48Ti ratios and inferred initial 26Al/27Al ratios of the low-density graphite spherules, even at subsolar 12C/13C ratios. Due to the relatively large proportion of material from the Ni zone and the relative amounts of the two layers of the Ni zone required to meet these conditions, predicted 28Si excesses are larger than observed in the low-density graphite spherules, and large negative δ46Ti/48Ti, δ47Ti/48Ti, δ49Ti/48Ti and δ50Ti/48Ti are produced, in contrast to the observed normal δ46Ti/48Ti and δ47Ti/48Ti, large positive δ49Ti/48Ti and smaller positive δ50Ti/48Ti. Although better matches to the observed δ46Ti/48Ti, δ47Ti/48Ti and 28Si excesses can be found using much smaller amounts of Ni zone material and some Si/S zone material, it is very difficult to match simultaneously the Ti and Si isotopic compositions in any mixtures of material from these deep layers with He/C and He/N zone material, regardless of the condensation sequence. The occurrence of Fe-rich, Si-poor metal grains inside the graphite spherules does not have a satisfactory explanation.  相似文献   

11.
The black inclusion from the Krymka LL3 chondrite previously found to contain ‘mysterite’ by Lewiset al. (1979) belongs to a hitherto unknown class of carbonaceous chondrites. Its olivine and pyroxene compositions. Fo 97–99 and En 96, respectively, are characteristic of carbonaceous chondrites and its plagioclase composition. An 100, is characteristic of C3's. It contains a peculiar group of Co-, Cr-rich metal grains whose compositions are similar, but not identical, to those in C2 chondrites and which also bear some similarities to those in Renazzo. Its weight ratios of total FeSiO2 and solSiO2MgO are 0.74 and 1.43, respectively, and its atomic ratio of SiAl is 10.7, exactly the same as in carbonaceous chondrites. Its bulk chemical composition is very close to that of the Murchison C2 chondrite. The association of mysterite with a special type of carbonaceous chondrite material suggests that mysterite formed by low-temperature condensation in a different region of the nebula from other carbonaceous chondrites.  相似文献   

12.
We report the development of a new analytical system allowing the fully automated measurement of isotopic ratios in micrometer-sized particles by secondary ion mass spectrometry (SIMS) in a Cameca ims-6f ion microprobe. Scanning ion images and image processing algorithms are used to locate individual particles dispersed on sample substrates. The primary ion beam is electrostatically deflected to and focused onto each particle in turn, followed by a peak-jumping isotopic measurement. Automatic measurements of terrestrial standards indicate similar analytical uncertainties to traditional manual particle analyses (e.g., ∼3‰/amu for Si isotopic ratios). We also present an initial application of the measurement system to obtain Si and C isotopic ratios for ∼3300 presolar SiC grains from the Murchison CM2 carbonaceous chondrite. Three rare presolar Si3N4 grains were also identified and analyzed. Most of the analyzed grains were extracted from the host meteorite using a new chemical dissolution procedure. The isotopic data are broadly consistent with previous observations of presolar SiC in the same size range (∼0.5-4 μm). Members of the previously identified SiC AB, X, Y, and Z subgroups were identified, as was a highly unusual grain with an extreme 30Si enrichment, a modest 29Si enrichment, and isotopically light C. The stellar source responsible for this grain is likely to have been a supernova. Minor differences in isotopic distributions between the present work and prior data can be partially explained by terrestrial contamination and grain aggregation on sample mounts, though some of the differences are probably intrinsic to the samples. We use the large new SiC database to explore the relationships between three previously identified isotopic subgroups—mainstream, Y, and Z grains—all believed to originate in asymptotic giant branch stars. The isotopic data for Z grains suggest that their parent stars experienced strong CNO-cycle nucleosynthesis during the early asymptotic giant branch phase, consistent with either cool bottom processing in low-mass (M < 2.3M⊙) parent stars or hot-bottom burning in intermediate-mass stars (M > 4M⊙). The data provide evidence for a sharp threshold in metallicity, above which SiC grains form with much higher 12C/13C ratios than below. Above this threshold, the fraction of grains with relatively high 12C/13C decreases exponentially with increasing 29Si/28Si ratio. This result indicates a sharp increase in the maximum mass of SiC parent stars with decreasing metallicity, in contrast to expectations from Galactic chemical evolution theory.  相似文献   

13.
We report on the mineralogy, petrography, and in situ oxygen isotopic composition of twenty-five ultrarefractory calcium-aluminum-rich inclusions (UR CAIs) in CM2, CR2, CH3.0, CV3.1–3.6, CO3.0–3.6, MAC 88107 (CO3.1-like), and Acfer 094 (C3.0 ungrouped) carbonaceous chondrites. The UR CAIs studied are typically small, < 100 μm in size, and contain, sometimes dominated by, Zr-, Sc-, and Y-rich minerals, including allendeite (Sc4Zr3O12), and an unnamed ((Ti,Mg,Sc,Al)3O5) mineral, davisite (CaScAlSiO6), eringaite (Ca3(Sc,Y,Ti)2Si3O12), kangite ((Sc,Ti,Al,Zr,Mg,Ca,□)2O3), lakargiite (CaZrO3), warkite (Ca2Sc6Al6O20), panguite ((Ti,Al,Sc,Mg,Zr,Ca)1.8O3), Y-rich perovskite ((Ca,Y)TiO3), tazheranite ((Zr,Ti,Ca)O2−x), thortveitite (Sc2Si2O7), zirconolite (orthorhombic CaZrTi2O7), and zirkelite (cubic CaZrTi2O7). These minerals are often associated with 50–200 nm-sized nuggets of platinum group elements. The UR CAIs occur as: (i) individual irregularly-shaped, nodular-like inclusions; (ii) constituents of unmelted refractory inclusions – amoeboid olivine aggregates (AOAs) and Fluffy Type A CAIs; (iii) relict inclusions in coarse-grained igneous CAIs (forsterite-bearing Type Bs and compact Type As); and (iv) relict inclusions in chondrules. Most UR CAIs, except for relict inclusions, are surrounded by single or multilayered Wark-Lovering rims composed of Sc-rich clinopyroxene, ±eringaite, Al-diopside, and ±forsterite. Most of UR CAIs in carbonaceous chondrites of petrologic types 2–3.0 are uniformly 16O-rich (Δ17O ∼ −23‰), except for one CH UR CAI, which is uniformly 16O-depleted (Δ 17O ∼ −5‰). Two UR CAIs in Murchison have heterogeneous Δ17O. These include: an intergrowth of corundum (∼ ‒24‰) and (Ti,Mg,Sc,Al)3O5 (∼ 0‰), and a thortveitite-bearing CAI (∼ −20 to ∼ ‒5‰); the latter apparently experienced incomplete melting during chondrule formation. In contrast, most UR CAIs in metamorphosed chondrites are isotopically heterogeneous (Δ17O ranges from ∼ −23‰ to ∼ −2‰), with Zr- and Sc-rich oxides and silicates, melilite and perovskite being 16O-depleted to various degrees relative to uniformly 16O-rich (Δ17O ∼ −23‰) hibonite, spinel, Al-diopside, and forsterite. We conclude that UR CAIs formed by evaporation/condensation, aggregation and, in some cases, melting processes in a 16O-rich gas of approximately solar composition in the CAI-forming region(s), most likely near the protoSun, and were subsequently dispersed throughout the protoplanetary disk. One of the CH UR CAIs formed in an 16O-depleted gaseous reservoir providing an evidence for large variations in Δ17O of the nebular gas in the CH CAIs-forming region. Subsequently some UR CAIs experienced oxygen isotopic exchange during melting in 16O-depleted regions of the disk, most likely during the epoch of chondrule formation. In addition, UR CAIs in metamorphosed CO and CV chondrites, and, possibly, the corundum-(Ti,Mg,Sc,Al)3O5 intergrowth in Murchison experienced O-isotope exchange with aqueous fluids on the CO, CV, and CM chondrite parent asteroids. Thus, both nebular and planetary exchange with 16O-depleted reservoirs occurred.  相似文献   

14.
We report in situ ion microprobe analyses of oxygen isotopic compositions of olivine, low-Ca pyroxene, high-Ca pyroxene, anorthitic plagioclase, glassy mesostasis, and spinel in five aluminum-rich chondrules and nine ferromagnesian chondrules from the CR carbonaceous chondrites EET92042, GRA95229, and MAC87320. Ferromagnesian chondrules are isotopically homogeneous within ±2‰ in Δ17O; the interchondrule variations in Δ17O range from 0 to −5‰. Small oxygen isotopic heterogeneities found in two ferromagnesian chondrules are due to the presence of relict olivine grains. In contrast, two out of five aluminum-rich chondrules are isotopically heterogeneous with Δ17O values ranging from −6 to −15‰ and from −2 to −11‰, respectively. This isotopic heterogeneity is due to the presence of 16O-enriched spinel and anorthite (Δ17O = −10 to −15‰), which are relict phases of Ca,Al-rich inclusions (CAIs) incorporated into chondrule precursors and incompletely melted during chondrule formation. These observations and the high abundance of relict CAIs in the aluminum-rich chondrules suggest a close genetic relationship between these objects: aluminum-rich chondrules formed by melting of spinel-anorthite-pyroxene CAIs mixed with ferromagnesian precursors compositionally similar to magnesium-rich (Type I) chondrules. The aluminum-rich chondrules without relict CAIs have oxygen isotopic compositions (Δ17O = −2 to −8‰) similar to those of ferromagnesian chondrules. In contrast to the aluminum-rich chondrules from ordinary chondrites, those from CRs plot on a three-oxygen isotope diagram along the carbonaceous chondrite anhydrous mineral line and form a continuum with amoeboid olivine aggregates and CAIs from CRs. We conclude that oxygen isotope compositions of chondrules resulted from two processes: homogenization of isotopically heterogeneous materials during chondrule melting and oxygen isotopic exchange between chondrule melt and 16O-poor nebular gas.  相似文献   

15.
We report a study of the oxygen isotope ratios of chondrules and their constituent mineral grains from the Mokoia, oxidized CV3 chondrite. Bulk oxygen isotope ratios of 23 individual chondrules were determined by laser ablation fluorination, and oxygen isotope ratios of individual grains, mostly olivine, were obtained in situ on polished mounts using secondary ion mass spectrometry (SIMS). Our results can be compared with data obtained previously for the oxidized CV3 chondrite, Allende. Bulk oxygen isotope ratios of Mokoia chondrules form an array on an oxygen three-isotope plot that is subparallel to, and slightly displaced from, the CCAM (carbonaceous chondrite anhydrous minerals) line. The best-fit line for all CV3 chondrite chondrules has a slope of 0.99, and is displaced significantly (by δ17O ∼ −2.5‰) from the Young and Russell slope-one line for unaltered calcium-aluminum-rich inclusion (CAI) minerals. Oxygen isotope ratios of many bulk CAIs also lie on the CV-chondrule line, which is the most relevant oxygen isotope array for most CV chondrite components. Bulk oxygen isotope ratios of most chondrules in Mokoia have δ18O values around 0‰, and olivine grains in these chondrules have similar oxygen isotope ratios to their bulk values. In general, it appears that chondrule mesostases have higher δ18O values than olivines in the same chondrules. Our bulk chondrule data spread to lower δ18O values than any ferromagnesian chondrules that have been measured previously. Two chondrules with the lowest bulk δ18O values (−7.5‰ and −11.7‰) contain olivine grains that display an extremely wide range of oxygen isotope ratios, down to δ17O, δ18O around -50‰ in one chondrule. In these chondrules, there are no apparent relict grains, and essentially no relationships between olivine compositions, which are homogeneous, and oxygen isotopic compositions of individual grains. Heterogeneity of oxygen isotope ratios within these chondrules may be the result of incorporation of relict grains from objects such as amoeboid olivine aggregates, followed by solid-state chemical diffusion without concomitant oxygen equilibration. Alternatively, oxygen isotope exchange between an 16O-rich precursor and an 16O-poor gas may have taken place during chondrule formation, and these chondrules may represent partially equilibrated systems in which isotopic heterogeneities became frozen into the crystallizing olivine grains. If this is the case, we can infer that the earliest nebular solids from which chondrules formed had δ17O and δ18O values around -50‰, similar to those observed in refractory inclusions.  相似文献   

16.
We present oxygen isotope measurements of 28 unmelted Antarctic micrometeorites measuring 150-250 μm (long axis) collected in the South Pole water well. The micrometeorites were all unmelted and classified as either fine-grained, scoriaceous, coarse-grained or composite (a mix of two other classes). Spot analyses were made of each micrometeorite type using an ion microprobe. The oxygen isotope values were measured relative to standard mean ocean water (SMOW) and range from δ18O = 3‰ to 60‰ and δ17O = −1‰ to 32‰, falling along the terrestrial fractionation line (TFL) within 2σ errors. Several analytical spots (comprising multiple phases) were made on each particle. Variability in the oxygen isotope ratios was observed among micrometeorite types, between micrometeorites of the same type and between analytical spots on a single micrometeorite indicating that micrometeorites are isotopically heterogeneous. In general, the lowest isotope values are associated with the coarse-grained micrometeorites whereas most of the fine-grained and scoriaceous micrometeorites have an average δ18O ? 22‰, suggesting that the matrix in micrometeorites is isotopically heavier than the anhydrous silicate phases. The oxygen isotope values for the coarse-grained micrometeorites, composed mainly of anhydrous phases, do not lie along the carbonaceous chondrite anhydrous mineral (CCAM) line, as observed for olivines, pyroxenes and some kinds of chondrules in carbonaceous chondrites, suggesting that coarse-grained MMs are not related to chondrules, as previously thought. Our measurements span the same range as values found for melted micrometeorites in other studies. Although four of the micrometeorites have oxygen isotope values lying along the TFL, close to the region where the bulk CI carbonaceous chondrites are found, 21 particles have very enriched 17O and 18O values that have not been reported in previous analyses of chondrite matrix material, suggesting that they could be a new type of Solar System object. The parent bodies of the micrometeorites with higher 18O values may be thermal metamorphosed carbonaceous asteroids that have not been found as meteorites either because they are friable asteroids that produce small particles rather than rocks upon collision with other bodies, or because the rocks they produce are too friable to survive atmospheric entry.  相似文献   

17.
The oxygen isotopic micro-distributions within and among minerals in a coarse-grained Ca, Al-rich inclusion (CAI), 7R-19-1 from the Allende meteorite, were measured by in situ using secondary ion mass spectrometry (SIMS). All values of O isotopic ratios in 7R-19-1 minerals fall along the carbonaceous chondrite anhydrous mineral mixing (CCAM) line on a δ17OSMOW vs. δ18OSMOW plot. Major refractory minerals (spinel, fassaite and melilite) in 7R-19-1 showed large negative anomalies of Δ17O in the order, spinel (−21‰) > 16O-rich melilite (∼−18‰) > fassaite (−15 to +1‰) > 16O-poor melilite (−8 to +2‰). However, the lower limit values of Δ17O are similar at about −21‰, a value commonly observed in CAIs. The similarity in the extreme values of the isotope anomaly anomalies suggests that crystallization of all CAIs started from an 16O enrichment of 21‰ (Δ17O) relative to terrestrial values. The order of the O isotopic anomalies observed for 7R-19-1, except for 16O-poor melilite, is parallel to the crystallization sequence determined by experiment from CAI liquid (Stolper, 1982), indicating that the O isotopic exchange in 7R-19-1 occurred between CAI melt and surrounding gas while 7R-19-1 was crystallizing from the 16O enriched CAI liquid (∼−21‰ in Δ17O) in the 16O-poor solar nebula. However, the a single crystallization sequence during the cooling stage cannot explain the existence of 16O-poor melilite. The presence of 16O-poor melilite suggests that multiple heating events occurred during CAI formation. The sharp contact between 16O-rich and 16O-poor melilite crystals and within 16O-rich melilite indicates that these multiple heatings occurred quickly. Based on the O isotopic and chemical compositions, fassaite crystals were aggregates of relic crystals formed from CAI melt whichthat have had various O isotopic compositions from the remelting processes. The results of intra-mineral distributions of O isotopes also support multiple heating events during CAI formation.  相似文献   

18.
Refractory inclusions, or CAIs (calcium-aluminium-rich inclusions) are a unique ingredient in chondritic meteorites. As the name suggests, they are enriched in refractory elements, essentially reflecting a condensation sequence of phases from a cooling gas of solar composition. However, the widespread preservation of diverse isotopic anomalies is not compatible with the inclusions having been in a gaseous form. Rather, the CAIs appear to represent mixtures of condensate and refractory residue materials. The condensates formed from cooling solar gas and fractionation of that gas produced variations in the abundances of refractory elements according to volatility. Solar condensate has isotopically normal Ca and Ti isotopic compositions and has 26Al/27Al of the canonical value for the solar system at 5 × 10?5. Residues of material falling in toward the Sun are probably aluminous oxides such as corundum and hibonite, and preserve diverse Ca and Ti isotopic anomalies. Meteoritic inclusions from the Murchison meteorite show the best polarization of these components. Spinel-hibonite-perovskite inclusions (SHIBs) predominantly have normal Ca and Ti isotopes, 26Al/27Al at 5 × 10?5, and ultrarefractory fractionated REE patterns. Single hibonite crystal fragments (PLACs) have diverse Ca and Ti isotopic compositions and low 26Al/27Al because of the initially high proportion of 27Al in the residue. REE patterns in PLACs are variable in terms of the ultrarefractory fractionation of their REE patterns, as indicated by Tm/Tm?, but are dominated by depletion in the less refractory REE Eu and Yb. Both PLACs and SHIBs homogenized with 16O-rich gas, enriched relative to terrestrial O by up to 7%, thus removing any isotopic heterogeneity from the PLAC precursors. CAIs formed close to the Sun where condensation and re-evaporation of REE was possible, and were then ejected back to planetary radii where they were eventually accreted onto planetesimals.  相似文献   

19.
The abundant, diverse ureilite meteorites are peridotitic asteroidal mantle restites that have remarkably high bulk carbon contents (average 3 wt%) and have long been linked to the so-called carbonaceous chondrites (although this term is potentially misleading, because the high petrologic type “carbonaceous” chondrites are, if anything, C-poor compared to ordinary chondrites). Ureilite oxygen isotopic compositions, i.e., diversely negative (CCAM-like) Δ17O, viewed in isolation, have long been viewed as confirming the carbonaceous-chondritic derivation hypothesis. However, a very different picture emerges through analysis of a compilation of recently published high-precision isotopic data for chromium, titanium and nickel for ureilites and various other planetary materials. Ureilites have lower ε62Ni and far lower ε50Ti and ε54Cr than any known variety of carbonaceous chondrite. On a plot of ε50Ti vs. ε54Cr, and similarly Δ17O vs. ε54Cr, ureilite compositions cluster far from and in a direction approximately orthogonal to a trend internal to the carbonaceous chondrites, and the carbonaceous chondrites are separated by a wide margin from all other planetary materials. I conclude that notwithstanding the impressive resemblance to carbonaceous chondrites in terms of diversely negative Δ17O, the ureilite precursors accreted from preponderantly noncarbonaceous (sensu stricto) materials. Despite total depletion of basaltic matter, the ureilites retain moderate pyroxene/olivine ratios; which is an expected outcome from simple partial melting of moderate-SiO2/(FeO + MgO) noncarbonaceous chondritic material, but would imply an additional process of major reduction of FeO if the precursor material were carbonaceous-chondritic. The striking bimodality of planetary materials on the ε50Ti vs. ε54Cr and Δ17O vs. ε54Cr diagrams may be an extreme manifestation of the effects of episodic accretion of early solids in the protoplanetary nebula. However, an alternative, admittedly speculative, explanation is that the bimodality corresponds to a division between materials that originally accreted in the outer solar system (carbonaceous) and materials that accreted in the inner solar system (noncarbonaceous, including the ureilites).  相似文献   

20.
We examined oxygen three-isotope ratios of 48 extraterrestrial chromite (EC) grains extracted from mid-Ordovician sediments from two different locations in Sweden, and one location in south-central China. The ages of the sediments (∼470 Ma) coincide with the breakup event of the L chondrite parent asteroid. Elemental compositions of the chromite grains are generally consistent with their origin from L or LL chondrite parent bodies. The average Δ17O (‰-deviation from the terrestrial mass-fractionation line, measured in situ from 15 μm spots by secondary ion mass spectrometry; SIMS) of EC grains extracted from fossil meteorites from Thorsberg and Brunflo are 1.17 ± 0.09‰ (2σ) and 1.25 ± 0.16‰, respectively, and those of fossil micrometeorites from Thorsberg and Puxi River are 1.10 ± 0.09‰, and 1.11 ± 0.12‰, respectively. Within uncertainty these values are all the same and consistent with the L chondrite group average Δ17O = 1.07 ± 0.18‰, but also with the LL chondrite group average Δ17O = 1.26 ± 0.24‰ (Clayton et al., 1991). We conclude that the studied EC grains from correlated sediments from Sweden and China are related, and most likely originated in the same event, the L chondrite parent body breakup. We also analyzed chromites of modern H, L and LL chondrites and show that their Δ17O values coincide with averages of Δ17O of bulk analyses of H, L and LL chondrites. This study demonstrates that in situ oxygen isotope data measured by SIMS are accurate and precise if carefully standardized, and can be used to classify individual extraterrestrial chromite grains found in sediments.  相似文献   

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