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1.
Seventy-one carbonaceous chondritic microclasts of average size 150 μm have been found in three howardites (Yamato-793497, Jodzie, Kapoeta). All carbonaceous chondritic microclasts are made of a fine-grained phyllosilicate-rich matrix supporting a variety of minerals such as olivine, pyroxene, spinel, iron oxides, iron-nickel sulfides, and calcium carbonates. Such a mineralogy is typical of chondritic C2 matter. Half of the carbonaceous chondritic microclasts are tochilinite-rich, and have been tentatively called CM2 microclasts. The other half are magnetite-rich, and have been tentatively called CR2 microclasts. The absence of a correlation between the CM2/CR2 ratio in carbonaceous chondritic microclasts and in numerous millimeter-sized clasts found in the same sections argues for carbonaceous chondritic microclasts being true micrometeorites rather than fragments of larger objects. Dynamical simulations show that it is possible for asteroidal dust to encounter Vesta (the howardite’s putative parent-asteroid) at velocity low enough (<1 km.s−1) to prevent fragmentation. Because the micrometeorite flux in the inner Solar System has been decreasing with time, we argue that carbonaceous chondritic microclasts have been trapped in Vesta’s regolith early in the history of the Solar System and are fossil micrometeorites. Because both microclasts and clasts found in howardites are related to C2 chondritic matter, we propose that C2 matter represents the bulk, or at least a significant fraction of the primordial howardite parent-asteroid. Considering the abundance of C2 matter among fossil micrometeorites, we speculate that the C2 fossil micrometorites are the so far unidentified agent of the late chondritic veneer that endowed the Earth’s mantle with an excess of siderophile elements relative to the contents predicted by the core-mantle separation models. The discovery that C2 fossil micrometeorites are similar to C2 modern Antarctic micrometeorites supports recent models proposing a micrometeoritic origin for the Earth’s oceans and volatile species.  相似文献   

2.
Oxygen isotopes were measured in four chondritic hydrated interplanetary dust particles (IDPs) and five chondritic anhydrous IDPs including two GEMS-rich particles (Glass embedded with metal and sulfides) by a combination of high precision and high lateral resolution ion microprobe techniques.All IDPs have isotopic compositions tightly clustered around that of solar system planetary materials. Hydrated IDPs have mass-fractionated oxygen isotopic compositions similar to those of CI and CM carbonaceous chondrites, consistent with hydration of initially anhydrous protosolar dust. Anhydrous IDPs have small 16O excesses and depletions similar to those of carbonaceous chondrites, the largest 16O variations being hosted by the two GEMS-rich IDPs. Coarse-grained forsteritic olivine and enstatite in anhydrous IDPs are isotopically similar to their counterparts in comet Wild 2 and in chondrules suggesting a high temperature inner solar system origin. The small variations in the 16O content of GEMS-rich IDPs suggest that most GEMS either do not preserve a record of interstellar processes or the initial interstellar dust is not 16O-rich as expected by self-shielding models, although a larger dataset is required to verify these conclusions.Together with other chemical and mineralogical indicators, O isotopes show that the parent-bodies of carbonaceous chondrites, of chondritic IDPs, of most Antarctic micrometeorites, and comet Wild 2 belong to a single family of objects of carbonaceous chondrite chemical affinity as distinct from ordinary, enstatite, K- and R-chondrites. Comparison with astronomical observations thus suggests a chemical continuum of objects including main belt and outer solar system asteroids such as C-type, P-type and D-type asteroids, Trojans and Centaurs as well as short-period comets and other Kuiper Belt Objects.  相似文献   

3.
Magnesium isotopic composition of the Earth and chondrites   总被引：3，自引：0，他引：3  
To constrain further the Mg isotopic composition of the Earth and chondrites, and investigate the behavior of Mg isotopes during planetary formation and magmatic processes, we report high-precision (±0.06‰ on δ25Mg and ±0.07‰ on δ26Mg, 2SD) analyses of Mg isotopes for (1) 47 mid-ocean ridge basalts covering global major ridge segments and spanning a broad range in latitudes, geochemical and radiogenic isotopic compositions; (2) 63 ocean island basalts from Hawaii (Kilauea, Koolau and Loihi) and French Polynesia (Society Island and Cook-Austral chain); (3) 29 peridotite xenoliths from Australia, China, France, Tanzania and USA; and (4) 38 carbonaceous, ordinary and enstatite chondrites including 9 chondrite groups (CI, CM, CO, CV, L, LL, H, EH and EL).Oceanic basalts and peridotite xenoliths have similar Mg isotopic compositions, with average values of δ25Mg = −0.13 ± 0.05 (2SD) and δ26Mg = −0.26 ± 0.07 (2SD) for global oceanic basalts (n = 110) and δ25Mg = −0.13 ± 0.03 (2SD) and δ26Mg = −0.25 ± 0.04 (2SD) for global peridotite xenoliths (n = 29). The identical Mg isotopic compositions in oceanic basalts and peridotites suggest that equilibrium Mg isotope fractionation during partial melting of peridotite mantle and magmatic differentiation of basaltic magma is negligible. Thirty-eight chondrites have indistinguishable Mg isotopic compositions, with δ25Mg = −0.15 ± 0.04 (2SD) and δ26Mg = −0.28 ± 0.06 (2SD). The constancy of Mg isotopic compositions in all major types of chondrites suggest that primary and secondary processes that affected the chemical and oxygen isotopic compositions of chondrites did not significantly fractionate Mg isotopes.Collectively, the Mg isotopic composition of the Earth’s mantle, based on oceanic basalts and peridotites, is estimated to be −0.13 ± 0.04 for δ25Mg and −0.25 ± 0.07 for δ26Mg (2SD, n = 139). The Mg isotopic composition of the Earth, as represented by the mantle, is similar to chondrites. The chondritic composition of the Earth implies that Mg isotopes were well mixed during accretion of the inner solar system.  相似文献   

4.
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   

5.
Atmospheric composition is a key control on climate and the habitability of planetary surfaces. Ablation of infalling micrometeorites has been recognised as one way in which atmospheric chemistry can be changed, especially at times in solar system history when the infall rates of exogenous material were high. Despite its potential to influence climate and habitability, extraterrestrial sulphur dioxide is currently an unquantified contribution to the atmospheres of the terrestrial planets. We have used flash pyrolysis to simulate the atmospheric entry of micrometeorites and Fourier-transform infrared spectroscopy to identify and quantify the sulphur dioxide produced from the carbonaceous meteorites Orgueil (CI1), ALH 88045 (CM1), Cold Bokkeveld (CM2), Murchison (CM2) and Mokoia (CV3). We have used this approach to understand the introduction of sulphur dioxide to the atmospheres of Earth and Mars from infalling micrometeorites. Sulphates, present in carbonaceous chondrites at a few wt.%, are resistant to thermal decomposition, limiting the yields of sulphur dioxide from unmelted micrometeorites. Infalling micrometeorites are a minor source of present-day sulphur dioxide on Earth and Mars, calculated to be up to around 2400 tonnes and about 350 tonnes, respectively. During the Late Heavy Bombardment (LHB), the much greater infall rates of micrometeoritic dust are calculated to be associated with average production rates of sulphur dioxide of around 20 Mt yr−1 for the early Earth and 0.5 Mt yr−1 for early Mars, for a LHB of 100 Myr. These rates of delivery of sulphur dioxide at high altitudes would have reduced the solar energy reaching the surfaces of these planets, via scattering of sunlight by stratospheric sulphate aerosols, and may have had detrimental effects on developing biospheres by promoting cooler climates and reducing the probability of liquid water on planetary surfaces.  相似文献   

6.
Ion microprobe measurements of D/H ratios in individual fragments of eight stratospheric dust particles give δD values ranging from ?386 to +2534‰ relative to SMOW. The δD values in five particles far exceed those in terrestrial samples and prove that the samples are interplanetary dust particles (IDPs). The hydrogen isotopic composition is heterogeneous on a scale of a few microns demonstrating that the dust is unequilibrated. Measurements of D/H ratios in conjunction with elemental and molecular ion signals in different fragments of individual IDPs show that a carbonaceous phase, not water, is the carrier of the D enrichments. Previous infrared transmission measurements have shown that IDPs fall into three main spectral classes. Particles from two of those three IR classes show large D/H ratios. Two particles studied from the third class do not. However, one of these contains solar flare tracks and is extraterrestrial. Thus, most, but not all, IDPs contain hydrogen with a non-terrestrial isotopic composition.Carbon isotopic measurements on fragments of three IDPs give ratios similar to terrestrial values and show a largely uniform isotopic composition for a given particle. Small, but significant, differences in δ13C of ~40‰ between particles are seen. No correlations between the hydrogen and carbon isotopic compositions are observed.The magnesium and silicon isotopic compositions of fragments of three IDPs are found to be normal within measurement errors.  相似文献   

7.
The Moon is thought to have formed after a planetary embryo, known as Theia, collided with the proto-Earth 4.5 billion years ago. This so-called Giant Impact was the last major event during Earth’s accretion, and its effects on the composition of the Earth and the newly forming Moon would be measureable today. Recent work on lunar samples has revealed that the Moon’s water was not lost as a result of this giant impact. Instead, the Moon appears to contain multiple hydrogen reservoirs with diverse deuterium-to-hydrogen (D/H) ratios. For the first time, we incorporate hydrogen isotopic measurements of lunar samples to help constrain the composition of Theia. We show that the Moon incorporated very low-D/H (δD ≈ -750‰) materials that only could have derived from solar nebula H2 ingassed into the magma ocean of a large (∼0.4 ME) planetary embryo that was largely devoid of chondritic water. We infer Theia was a very large body comparable in size to the proto-Earth, and was composed almost entirely of enstatite chondrite-like material. These conclusions limit the type of impact to a “merger” model of similarly-sized bodies, or possibly a “hit-and-run” model, and they rule out models that mix isotopes too effectively.  相似文献   

8.
Nitrogen concentrations and isotopic compositions were measured by ion microprobe scanning imaging in two interplanetary dust particles L2021 K1 and L2036 E22, in which imaging of D/H and C/H ratios has previously evidenced the presence of D-rich macromolecular organic components. High nitrogen concentrations of 10-20 wt% and δ15N values up to +400‰ are observed in these D-rich macromolecular components. The previous study of D/H and C/H ratios has revealed three different D-rich macromolecular phases. The one previously ascribed to macromolecular organic matter akin the insoluble organic matter (IOM) from carbonaceous chondrites is enriched in nitrogen by one order of magnitude compared to the carbonaceous chondrite IOM, although its isotopic composition is still similar to what is known from Renazzo (δ15N = +208‰).The correlation observed in macromolecular organic material between the D- and 15N-excesses suggests that the latter originate probably from chemical reactions typical of the cold interstellar medium. These interstellar materials preserved to some extent in IDPs are therefore macromolecular organic components with various aliphaticity and aromaticity. They are heavily N-heterosubstituted as shown by their high nitrogen concentrations >10 wt%. They have high D/H ratios >10−3 and δ15N values ≥ +400‰. In L2021 K1 a mixture is observed at the micron scale between interstellar and chondritic-like organic phases. This indicates that some IDPs contain organic materials processed at various heliocentric distances in a turbulent nebula. Comparison with observation in comets suggests that these molecules may be cometary macromolecules. A correlation is observed between the D/H ratios and δ15N values of macromolecular organic matter from IDPs, meteorites, the Earth and of major nebular reservoirs. This suggests that most macromolecular organic matter in the inner solar system was probably issued from interstellar precursors and further processed in the protosolar nebula.  相似文献   

9.
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   

10.
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   

11.
The insoluble organic matter of the carbonaceous meteorites contains radicals having a polyaromatic structure and a heterogeneous distribution. By using Hyperfine Sublevel Correlation spectroscopy (HYSCORE) in pulsed Electron Paramagnetic Resonance (pulsed-EPR), whereby nuclear frequencies of magnetic nuclei and their hyperfine interaction with electron spin of radicals are detected with high resolution, the radicals are shown to be considerably enriched in deuterium in the Orgueil meteorite, with a D/H ratio of 1.5 ± 0.5 × 10−2. These radicals hold 3.6 ± 1.2 × 10−3 H relative to total organic H.Analysis of hydrogen and deuterium hyperfine interactions indicates that the deuterium atoms are localized in the benzylic position, on aliphatic carbons bonded to aromatic radical moieties. This type of C-H bond exhibits one of the smallest bond energy, reinforcing the recent finding that the lower the C-H bond energy the higher the deuterium-enrichment (Remusat L., Palhol F., Robert F., Derenne S. and France-Lanord C. (2006) Enrichment of deuterium in insoluble organic matter from primitive meteorites: a solar system origin? Earth Planet. Sci. Lett.243, 15-25). Such a behavior is difficult to reconcile with the usual interpretation according to which high D/H ratios represent survivals of interstellar grains. More likely, the deuterium-enrichment process took place after the formation of organic grains whose initial isotopic compositions was close to the protosolar D/H ratio. These grains were possibly loaded at the surface of the protosolar disk where they exposed to the intense solar UV irradiation, triggering an isotopic exchange with deuterium-rich highly reactive ions.  相似文献   

12.
The metal-rich carbonaceous chondrites (CB and CH) have the highest whole-rock 15N-enrichments (δ15N up to 1500‰) among planetary materials. They are also characterized by the absence of interchondrule fine-grained matrix. The only fine-grained material is present as lithic clasts, which experienced extensive aqueous alteration in contrast to the surrounding high-temperature components (chondrules, refractory inclusions, metal grains). Hence, the clasts are foreign objects that were incorporated at a late stage into the final parent body of Isheyevo. Their origin is poorly constrained. Based on mineralogy, petrography, and thermal processing of the aromatic carbonaceous component, different types of clasts have been previously identified in the CB/CH-like chondrite Isheyevo. Here, we focus on the rare lithic clasts characterized by the presence of anhydrous silicates (chondrules, chondrule fragments, and CAIs). Their mineralogy and oxygen isotopic compositions reveal them to be micro-chondrules, fragments of chondrules, and refractory inclusions related to those in the Isheyevo host, suggesting accretion in the same region. In contrast to previously studied IDPs or primitive chondritic matrices, the fine-grained material in the clasts we studied is highly and rather uniformly enriched in heavy nitrogen, with bulk δ15N values ranging between 1000‰ and 1300‰. It is also characterized by the presence of numerous 15N hotspots (δ15N ranging from 1400‰ to 4000‰). No bulk (δD <-240‰) or localized deuterium enrichments were observed. These clasts have the highest bulk enrichment in heavy nitrogen measured to date in a fine-grained material. They represent a unique material, of asteroidal or cometary origin, in our collection of cosmomaterials. We show that they were 15N-enriched before their incorporation in the final parent body of Isheyevo. They experienced an extensive aqueous alteration that most likely played a role in redistributing 15N over the whole fine-grained material and may have significantly modified its initial hydrogen isotopic composition. Based on a review of isotopic fractionation models, we conclude that the nitrogen isotopic fractionation process, its timing, and its location are still poorly constrained. The 15N-rich clasts may represent the surviving original carrier of the 15N anomaly in Isheyevo whole-rock.  相似文献   

13.
Osmium isotopic compositions, and Re and Os concentrations have been examined in one komatiite unit and two komatiitic basalt units at Dundonald Beach, part of the 2.7 Ga Kidd-Munro volcanic assemblage in the Abitibi greenstone belt, Ontario, Canada. The komatiitic rocks in this locality record at least three episodes of alteration of Re-Os elemental and isotope systematics. First, an average of 40% and as much as 75% Re may have been lost due to shallow degassing during eruption and/or hydrothermal leaching during or immediately after emplacement. Second, the Re-Os isotope systematics of whole rock samples with 187Re/188Os ratios >1 were reset at ∼2.5 Ga, possibly due to a regional metamorphic event. Third, there is evidence for relatively recent gain and loss of Re in some rocks.Despite the open-system behavior, some aspects of the Re-Os systematics of these rocks can be deciphered. The bulk distribution coefficient for Os (DOssolid/liquid) for the Dundonald rocks is ∼3 ± 1 and is well within the estimated D values obtained for komatiites from the nearby Alexo area and stratigraphically-equivalent komatiites from Munro Township. This suggests that Os was moderately compatible during crystal-liquid fractionation of the magmas parental to the Kidd-Munro komatiitic rocks. Whole-rock samples and chromite separates with low 187Re/188Os ratios (<1) yield a precise chondritic average initial 187Os/188Os ratio of 0.1083 ± 0.0006 (γOs = 0.0 ± 0.6) for their well-constrained ∼2715 Ma crystallization age. The chondritic initial Os isotopic composition of the mantle source for the Dundonald rocks is consistent with that determined for komatiites in the Alexo area and in Munro Township, suggesting that the mantle source region for the Kidd-Munro volcanic assemblage had evolved with a long-term chondritic Re/Os before eruption. The chondritic initial Os isotopic composition of the Kidd-Munro komatiites is indistinguishable from that of the projected contemporaneous convective upper mantle. The uniform chondritic Os isotopic composition of the Kidd-Munro komatiites contrasts with the typical large-scale Os isotopic heterogeneity in the mantle sources for ca. 89 Ma komatiites from the Gorgona Island, arc-related rocks and present-day ocean island basalts. This suggests that the Kidd-Munro komatiites sampled a late-Archean mantle source region that was significantly more homogeneous with respect to Re/Os relative to most modern mantle-derived rocks.  相似文献   

14.
The composition of the Earth   总被引：317，自引：0，他引：317  
W. F. McDonough  S. -s. Sun   《Chemical Geology》1995,120(3-4):223-253
Compositional models of the Earth are critically dependent on three main sources of information: the seismic profile of the Earth and its interpretation, comparisons between primitive meteorites and the solar nebula composition, and chemical and petrological models of peridotite-basalt melting relationships. Whereas a family of compositional models for the Earth are permissible based on these methods, the model that is most consistent with the seismological and geodynamic structure of the Earth comprises an upper and lower mantle of similar composition, an Fe---Ni core having between 5% and 15% of a low-atomic-weight element, and a mantle which, when compared to CI carbonaceous chondrites, is depleted in Mg and Si relative to the refractory lithophile elements.The absolute and relative abundances of the refractory elements in carbonaceous, ordinary, and enstatite chondritic meteorites are compared. The bulk composition of an average CI carbonaceous chondrite is defined from previous compilations and from the refractory element compositions of different groups of chondrites. The absolute uncertainties in their refractory element compositions are evaluated by comparing ratios of these elements. These data are then used to evaluate existing models of the composition of the Silicate Earth.The systematic behavior of major and trace elements during differentiation of the mantle is used to constrain the Silicate Earth composition. Seemingly fertile peridotites have experienced a previous melting event that must be accounted for when developing these models. The approach taken here avoids unnecessary assumptions inherent in several existing models, and results in an internally consistent Silicate Earth composition having chondritic proportions of the refractory lithophile elements at 2.75 times that in CI carbonaceous chondrites. Element ratios in peridotites, komatiites, basalts and various crustal rocks are used to assess the abundances of both non-lithophile and non-refractory elements in the Silicate Earth. These data provide insights into the accretion processes of the Earth, the chemical evolution of the Earth's mantle, the effect of core formation, and indicate negligible exchange between the core and mantle throughout the geologic record (the last 3.5 Ga).The composition of the Earth's core is poorly constrained beyond its major constituents (i.e. an Fe---Ni alloy). Density contrasts between the inner and outer core boundary are used to suggest the presence ( 10 ± 5%) of a light element or a combination of elements (e.g., O, S, Si) in the outer core. The core is the dominant repository of siderophile elements in the Earth. The limits of our understanding of the core's composition (including the light-element component) depend on models of core formation and the class of chondritic meteorites we have chosen when constructing models of the bulk Earth's composition.The Earth has a bulk Fe/Al of 20 ± 2, established by assuming that the Earth's budget of Al is stored entirely within the Silicate Earth and Fe is partitioned between the Silicate Earth ( 14%) and the core ( 86%). Chondritic meteorites display a range of Fe/Al ratios, with many having a value close to 20. A comparison of the bulk composition of the Earth and chondritic meteorites reveals both similarities and differences, with the Earth being more strongly depleted in the more volatile elements. There is no group of meteorites that has a bulk composition matching that of the Earth's.  相似文献   

15.
DaG 896 is an olivine-rich microporphyritic rock of komatiitic composition. Both the olivine composition (Fa17.5±2.1, [Mn/Mg] = 0.0061) and the bulk oxygen isotopic composition (δ17O = +2.55, δ18O = +3.50) indicate that DaG 896 is a sample of the H-chondrite parent body. The bulk chemistry shows an H-chondritic distribution of lithophile elements, whereas chalcophile and siderophile elements are strongly depleted, indicating formation through whole-rock melting (or nearly so) of H-chondrite material, nearly complete loss of the metal plus sulfide component, and crystallization without significant igneous fractionation. Superheated, severely shocked chondritic relics (∼10 vol%), typically in the form of corroded lithic fragments <100 μm in size intimately distributed within the igneous lithology, indicate that melting was triggered by a highly energetic impact, which possibly induced shock pressures of ∼80-100 GPa. The relatively young 3.704 ± 0.035 Ga 40Ar-39Ar crystallization age is consistent with the impact melting origin, as magmatism in the asteroid belt was active only in the first hundred million years of solar system history.Based on textural data and thermodynamic crystallization modelling, we infer that DaG 896 crystallized from a liquidus temperature of ∼1630°C under relatively slow cooling rates (∼10°C h−1) to ∼1300°C, before quenching. The two-stage cooling history indicates that a reasonable formation environment might be a dike intruding cooler basement below a crater floor. Metal-silicate fractionation may have been accomplished, at least at the centimeter-scale of the studied meteorite sample, through differential acceleration of immiscible liquids of different density during the intense flow regimes associated with the excavation and modification stages of the cratering mechanism. Alternatively, DaG 896 may represent a surface sample of a differentiated melt body at the floor of an impact crater, as gravitational settling appears to be an effective process at the surface of a chondritic parent asteroid: for metal particles 1 to 10 mm in size, typically observed in partially differentiated impact melt rocks, Stokes’ Law indicates a settling velocity >1 m h −1 during the first few hours of crystallization on asteroidal bodies of >25 km radius.The ∼3.7 Ga age of DaG 896 nearly overlaps with the slightly older resetting ages of H-chondrites (all impact melts) available from the literature, indicating that the H-chondrite parent asteroid underwent extensive impact melting at the enduring of the cataclysmic bombardment of the early solar system. Such an age overlap may also indicate early disruption of the initial H-chondrite parent asteroid.The close similarity between the bulk composition and degassing age of DaG 896 and silicate inclusions in IIE iron meteorites is further evidence in support of a common origin by impact melting and metal-silicate segregation on the H-chondrite parent asteroid. Our new high-precision oxygen isotopic measurements of H-chondrites (Δ17O = 0.77 ± 0.04) should be extended to IIEs to verify this possible petrogenetic link.  相似文献   

16.
Eight interplanetary dust particles (IDPs) exhibiting a wide range of H and N isotopic anomalies have been studied by transmission electron microscopy, x-ray absorption near-edge structure spectroscopy, and Fourier-transform infrared spectroscopy. These anomalies are believed to have originated during chemical reactions in a cold molecular cloud that was the precursor to the Solar System. The chemical and mineralogical studies reported here thus constitute direct studies of preserved molecular cloud materials. The H and N isotopic anomalies are hosted by different hydrocarbons that reside in the abundant carbonaceous matrix of the IDPs. Infrared measurements constrain the major deuterium (D) host in the D-enriched IDPs to thermally labile aliphatic hydrocarbon groups attached to macromolecular material. Much of the large variation observed in D/H in this suite of IDPs reflects the variable loss of this labile component during atmospheric entry heating. IDPs with elevated 15N/14N ratios contain N in the form of amine (-NH2) functional groups that are likely attached to other molecules such as aromatic hydrocarbons. The host of the N isotopic anomalies is not as readily lost during entry heating as the D-rich material. Infrared analysis shows that while the organic matter in primitive anhydrous IDPs is similar to that observed in acid residues of primitive chondritic meteorites, the measured aromatic:aliphatic ratio is markedly lower in the IDPs.  相似文献   

17.
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   

18.
Initial 187Os/188Os isotopic compositions for geochronologically and geologically well -constrained 3.8-Ga spinel peridotites from the Itsaq Gneiss Complex of southern West Greenland and chromite separates from 3.46-Ga komatiites from the Pilbara region of Western Australia have been determined to investigate the osmium isotopic evolution of the early terrestrial mantle. The measured compositions of 187Os/188Os(0) = 0.10262 ± 2, from an olivine separate, and 0.10329 ± 3, for a spinel separate from ∼3.8-Ga peridotite G93/42, are the lowest yet reported from any terrestrial sample. The corrections for in situ decay over 3.8 Ga for these low Re/Os phases are minimal and change the isotopic compositions by only 0.5 and 2.2% for the spinel and the olivine, respectively, resulting in 187Os/188Os(3.8 Ga) = 0.1021 ± 0.0002 and 0.1009 ± 0.0002, respectively. These data extend direct measurement of Os isotopic compositions to much earlier periods of Earth history than previously documented and provide the best constraints on the Os isotopic composition of the early Archean terrestrial mantle. Analyses of Pilbara chromites yield 3.46-Ga mantle compositions of 0.1042 ± 0.0002 and 0.1051 ± 0.0002.These new data, combined with published initial Os isotopic compositions from late Archean and early Proterozoic samples, are compatible with the mantle, or at least portions of it, evolving from a solar system initially defined by meteorites to a modern composition of 187Os/188Os(0) = 0.1296 ± 0.0008 as previously suggested from peridotite xenolith data ( Meisel et al., 2001); the associated 187Re/188Os(0) = 0.435 ± 0.005. Thus, chondritic 187Os/188Os compositions were a feature of the upper mantle for at least 3.8 billion years, requiring chondritic Re/Os ratios to have been a characteristic of the very early terrestrial mantle. In contrast, nonchondritic initial compositions of some Archean komatiites demonstrate that Os isotopic heterogeneity is an ancient feature of plume materials, reflecting the development of variable Re/Os mantle sources early in Earth history.The lower average 187Os/188Os = 0.1247 for abyssal peridotites (Snow and Reisberg, 1995) indicate that not all regions of the modern mantle have evolved with the same Re/Os ratio. The relative sizes of the various reservoirs are unknown, although mass balance considerations can provide some general constraints. For example, if the unradiogenic 187Os/188Os modern abyssal peridotite compositions reflect the prevalent upper mantle composition, then the complementary high Re/Os basaltic reservoir must represent 20 to 40% by mass of the upper mantle (taken here as 50% of the entire mantle), depending on the mean storage age. The difficulties associated with efficient long-term storage of such large volumes of subducted basalt suggest that the majority of the upper mantle is not significantly Re-depleted. Rather, abyssal peridotites sample anomalous mantle regions.The existence of 3.8-Ga mantle peridotites with chondritic 187Os/188Os compositions and with Os concentrations similar to the mean abundances measured in modern peridotites places an upper limit on the timing of a late accretionary veneer. These observations require that any highly siderophile element -rich component must have been added to the Earth and transported into and grossly homogenized within the mantle by 3.8 Ga. Either large-scale mixing of impact materials occurred on very short (0-100 myr) timescales or (the interpretation preferred here) the late veneer of highly siderophile elements is unrelated to the lunar terminal cataclysm estimated to have occurred at ∼3.8 to 3.9 Ga.  相似文献   

19.
Here we report the elemental and isotopic compositions of the insoluble organic material (IOM) isolated from several previously unanalyzed meteorites, as well as the reanalyses of H isotopic compositions of some previously measured samples (Alexander et al., 2007). The IOM in ordinary chondrites (OCs) has very large D enrichments that increase with increasing metamorphism and decreasing H/C, the most extreme δD value measured being almost 12,000‰. We propose that such large isotopic fractionations could be produced in the OC parent bodies through the loss of isotopically very light H2 generated when Fe was oxidized by water at low temperatures (<200 °C). We suggest that similar isotopic fractionations were not generated in the IOM of CV and CO chondrites with similar metamorphic grades and IOM H/C ratios because proportionately less water was consumed during metamorphism, and the remaining water buffered the H isotopic composition of the IOM even a H was being lost from it.Hydrogen would also have been generated during the alteration of CI, CM and CR carbonaceous chondrites. The IOM in these meteorites exhibit a considerable range in isotopic compositions, but all are enriched in D, as well as 15N, relative to terrestrial values. We explore whether these enrichments could also have been produced by the loss of H2, but conclude that the most isotopically anomalous IOM compositions in meteorites from these groups are probably closest to their primordial values. The less isotopically anomalous IOM has probably been modified by parent body processes. The response of IOM to these processes was complex and varied, presumably reflecting differences in conditions within and between parent bodies.The D enrichments associated with H2 generation, along with exchange between D-rich IOM and water in the parent bodies, means that it is unlikely that any chondrites retain the primordial H isotopic composition of the water ice that they accreted. The H isotopic compositions of the most water-rich chondrites, the CMs and CIs, are probably the least modified and their compositions (δD ? −25‰) suggest that their water did not form at large radial distances from the Sun where ice is predicted to be very D-rich. Yet models to explain the O isotopic composition of inner Solar System bodies require that large amounts of ice were transported from the outer to the inner Solar System.  相似文献   

20.
The Re-Os isotopic systematics of two ca. 2.7-Ga komatiite flows from Belingwe, Zimbabwe are examined. Rhenium and Os concentrations in these rocks are similar to concentrations in other Archean, Proterozoic, and Phanerozoic komatiites. Despite the excellent preservation of primary magmatic minerals, the Re-Os systematics of whole-rock samples of the komatiites show open-system behavior. Consistent model ages for several whole-rock samples suggest a disturbance to the system during the Proterozoic. Despite the open-system behavior in the whole rocks, Re-Os systematics for concentrates of primary magmatic olivine and spinel indicate generally closed-system behavior since the magmatic event that produced the rocks. Regression of the data for the mineral concentrates yields an age of 2721 ± 21 Ga, which is consistent with Pb-Pb and Sm-Nd ages that have been previously reported for the komatiites (Chauvel et al., 1993), and an initial 187Os/188Os ratio of 0.11140 ± 84 (γOs = +2.8 ± 0.8).The 2 to 3% enrichment in 187Os/188Os ratio of the mantle source of the komatiites, relative to the chondritic composition of the contemporaneous convecting upper mantle, most likely reflects either the incorporation of substantially older (≥ 4.2 Ga), Re-rich recycled mafic crust into the mantle source of the komatiites or the contribution of suprachondritic Os to the source from the putative 187Os-enriched outer core. The former interpretation would indicate the Hadean formation and recycling of mafic crust. The latter interpretation would require early formation of a substantial inner core followed by upwelling of a mantle plume from the core-mantle boundary, at least as far back as the Late Archean. Either interpretation requires large-scale mantle convection during the first half of Earth history.  相似文献   

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