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31.
Abstract— Calcium‐aluminum‐rich inclusions (CAIs) were among the first solids in the solar system and were, similar to chondrules, created at very high temperatures. While in chondrules, trapped noble gases have recently been detected, the presence of trapped gases in CAIs is unclear but could have important implications for CAI formation and for early solar system evolution in general. To reassess this question, He, Ne, and Ar isotopes were measured in small, carefully separated and, thus, uncontaminated samples of CAIs from the CV3 chondrites Allende, Axtell, and Efremovka. The 20Ne/22Ne ratios of all CAIs studied here are <0.9, indicating the absence of trapped Ne as, e.g., Ne‐HL, Ne‐Q, or solar wind Ne. The 21Ne/22Ne ratios range from 0.86 to 0.72, with fine‐grained, more altered CAIs usually showing lower values than coarse‐grained, less altered CAIs. This is attributed to variable amounts of cosmogenic Ne produced from Na‐rich alteration phases rather than to the presence of Ne‐G or Ne‐R (essentially pure 22Ne) in the samples. Our interpretation is supported by model calculations of the isotopic composition of cosmogenic Ne in minerals common in CAIs. The 36Ar/38Ar ratios are between 0.7 and 4.8, with fine‐grained CAIs within one meteorite showing higher ratios than the coarse‐grained ones. This agrees with higher concentrations of cosmogenic 36Ar produced by neutron capture on 35Cl with subsequent β?‐decay in finer‐grained, more altered, and thus, more Cl‐rich CAIs than in coarser‐grained, less altered ones. Although our data do not strictly contradict the presence of small amounts of Ne‐G, Ne‐R, or trapped Ar in the CAIs, our noble gas signatures are most simply explained by cosmogenic production, mainly from Na‐, Ca‐, and Cl‐rich minerals.  相似文献   
32.
A detailed mineralogical and chemical study of Almahata Sitta fine‐grained ureilites (MS‐20, MS‐165, MS‐168) was performed to shed light on the origin of these lithologies and their sulfide and metal. The Almahata Sitta fine‐grained ureilites (silicates <30 μm grain size) show textural and chemical evidence for severe impact smelting as described for other fine‐grained ureilites. Highly reduced areas in Almahata Sitta fine‐grained ureilites show large (up to ~1 mm) Si‐bearing metal grains (up to ~4.5 wt% Si) and niningerite [Mg>0.5,(Mn,Fe)<0.5S] with some similarities to the mineralogy of enstatite (E) chondrites. Overall, metal grains show a large compositional variability in Ni and Si concentrations. Niningerite grains probably formed as a by‐product of smelting via sulfidation. The large Si‐Ni variation in fine‐grained ureilite metal could be the result of variable degrees of reduction during impact smelting, inherited from coarse‐grained ureilite precursors, or a combination of both. Large Si‐bearing metal grains probably formed via coalescence of existing and newly formed metal during impact smelting. Bulk and in situ siderophile trace element abundances indicate three distinct populations of (1) metal crystallized from partial melts in MS‐20, (2) metal resembling bulk chondritic compositions in MS‐165, and (3) residual metal in MS‐168. Almahata Sitta fine‐grained ureilites developed their distinctive mineralogy due to severe reduction during smelting. Despite the presence of E chondrite and ureilite stones in the Almahata Sitta fall, a mixing relation of E chondrites or their constituents and ureilite material in Almahata Sitta can be ruled out based on isotopic, textural, and mineral‐chemical reasons.  相似文献   
33.
Fragments in the size range from 40 μm to several hundred μm in the CI chondrites Orgueil, Ivuna, Alais, and Tonk show a wide range of chemical compositions with variations in major elements such as iron (10.4-42.4 wt% FeO), silicon (12.7-42.2 wt% SiO2), and sulfur (1.01-15.8 wt% SO3), but also important minor elements such as phosphorous (up to 5.2 wt% P2O5) or calcium (up to 6.6 wt% CaO). These variations are the result of the varying mineralogical compositions of these fragments. The distribution of phyllosilicates, magnetites, and possibly ferrihydrite, in particular, control the abundances of these elements. High REE contents—up to 150 times the solar abundances—were observed in phosphates, while matrix and sulfates are REE-depleted. The studied 113 fragments were subdivided into eight lithologies with similar mineralogical and thus chemical properties. The most common is the CGA lithology, consisting of a groundmass of Mg-rich, coarse-grained phyllosilicates and varying abundances of inclusions such as magnetite. The second most abundant lithology is the FGA lithology, consisting of a groundmass of fine-grained Fe-rich phyllosilicates. A rare, but important lithology consists of fragments with high contents of phosphates and other minerals. The proposed model for the evolution of these lithologies is based on a closed system alteration, where mineralogical differences in the lithologies reflect heterogeneities in the starting material. Comparison of our results with literature data indicates a general similarity of the four CI chondrites analyzed. Further comparison of bulk analyses suggests that the mass ‘threshold’ for chemical heterogeneities in CI chondrite samples is smaller than ∼1-2 g.  相似文献   
34.
Abstract– We present a detailed study of mineralogy, chemistry, and noble gases of the Neuschwanstein (EL6) chondrite that fell in 2002 in southern Germany. The meteorite has an unbrecciated texture and exhibits only minor shock features. Secondary weathering products are marginal. Neuschwanstein is an EL6 chondrite with heterogeneously distributed metal and sulfide grains. In terms of bulk chemistry, it has very high Fe concentrations, and siderophile and halogen element abundances higher than typical EL chondrites. However, like other ELs of higher petrologic type, it has low moderately volatile element abundances, e.g., Mn and Zn. We interpret these as indicators for loss of sulfide, probably through mobilization of ferroan alabandite and a Zn‐bearing sulfide, potentially sphalerite, during metamorphism. Trapped noble gases are dominated by a subsolar component with high Ar concentrations and are typical for EL chondrites. The shielding parameters indicate a small meteoroid (<20 cm radius) with an exposure age of approximately 47 Ma, which is among the highest for enstatite chondrites.  相似文献   
35.
We report both oxygen- and magnesium-isotope compositions measured in situ using a Cameca ims-1280 ion microprobe in 20 of 166 CAIs identified in 47 polished sections of 15 CR2 (Renazzo-type) carbonaceous chondrites. Two additional CAIs were measured for oxygen isotopes only. Most CR2 CAIs are mineralogically pristine; only few contain secondary phyllosilicates, sodalite, and carbonates - most likely products of aqueous alteration on the CR2 chondrite parent asteroid. Spinel, hibonite, grossite, anorthite, and melilite in 18 CAIs have 16O-rich (Δ17O = −23.3 ± 1.9‰, 2σ error) compositions and show no evidence for postcrystallization isotopic exchange commonly observed in CAIs from metamorphosed CV carbonaceous chondrites. The inferred initial 26Al/27Al ratios, (26Al/27Al)0, in 15 of 16 16O-rich CAIs measured are consistent with the canonical value of (4.5-5) × 10−5 and a short duration (<0.5 My) of CAI formation. These data do not support the “supra-canonical” values of (26Al/27Al)0 [(5.85-7) × 10−5] inferred from whole-rock and mineral isochrons of the CV CAIs. A hibonite-grossite-rich CAI El Djouf 001 MK #5 has uniformly 16O-rich (Δ17O = −23.0 ± 1.7‰) composition, but shows a deficit of 26Mg and no evidence for 26Al. Because this inclusion is 16O-rich, like CAIs with the canonical (26Al/27Al)0, we infer that it probably formed early, like typical CAIs, but from precursors with slightly nonsolar magnesium and lower-than-canonical 26Al abundance. Another 16O-enriched (Δ17O = −20.3 ± 1.2‰) inclusion, a spinel-melilite CAI fragment Gao-Guenie (b) #3, has highly-fractionated oxygen- and magnesium-isotope compositions (∼11 and 23‰/amu, respectively), a deficit of 26Mg, and a relatively low (26Al/27Al)0 = (2.0 ± 1.7) × 10−5. This could be the first FUN (Fractionation and Unidentified Nuclear effects) CAI found in CR2 chondrites. Because this inclusion is slightly 16O-depleted compared to most CR2 CAIs and has lower than the canonical (26Al/27Al)0, it may have experienced multistage formation from precursors with nonsolar magnesium-isotope composition and recorded evolution of oxygen-isotope composition in the early solar nebula over  My. Eight of the 166 CR2 CAIs identified are associated with chondrule materials, indicating that they experienced late-stage, incomplete melting during chondrule formation. Three of these CAIs show large variations in oxygen-isotope compositions (Δ17O ranges from −23.5‰ to −1.7‰), suggesting dilution by 16O-depleted chondrule material and possibly exchange with an 16O-poor (Δ17O > −5‰) nebular gas. The low inferred (26Al/27Al)0 ratios of these CAIs (<0.7 × 10−5) indicate melting >2 My after crystallization of CAIs with the canonical (26Al/27Al)0 and suggest evolution of the oxygen-isotope composition of the inner solar nebula on a similar or a shorter timescale. Because CAIs in CR2 and CV chondrites appear to have originated in a similarly 16O-rich reservoir and only a small number of CR2 and CV CAIs were affected by chondrule melting events in an 16O-poor gaseous reservoir, the commonly observed oxygen-isotope heterogeneity in CAIs from metamorphosed CV chondrites is most likely due to fluid-solid isotope exchange on the CV asteroidal body rather than gas-melt exchange. This conclusion does not preclude that some CV CAIs experienced oxygen-isotope exchange during remelting, instead it implies that such remelting is unlikely to be the dominant process responsible for oxygen-isotope heterogeneity in CV CAIs. The mineralogy, oxygen and magnesium-isotope compositions of CAIs in CR2 chondrites are different from those in the metal-rich, CH and CB carbonaceous chondrites, providing no justification for grouping CR, CH and CB chondrites into the CR clan.  相似文献   
36.
Abstract— Chondrules are generally believed to have lost most or all of their trapped noble gases during their formation. We tested this assumption by measuring He, Ne, and Ar in chondrules of the carbonaceous chondrites Allende (CV3), Leoville (CV3), Renazzo (CR2), and the ordinary chondrites Semarkona (LL3.0), Bishunpur (LL3.1), and Krymka (LL3.1). Additionally, metalsulfide‐rich chondrule coatings were measured that probably formed from chondrule metal. Low primordial 20Ne concentrations are present in some chondrules, while even most of them contain small amounts of primordial 36Ar. Our preferred interpretation is that‐in contrast to CAIs‐the heating of the chondrule precursor during chondrule formation was not intense enough to expel primordial noble gases quantitatively. Those chondrules containing both primordial 20Ne and 36Ar show low presolar‐diamond‐like 36Ar/20Ne ratios. In contrast, the metal‐sulfide‐rich coatings generally show higher gas concentrations and Q‐like 36Ar/20Ne ratios. We propose that during metalsilicate fractionation in the course of chondrule formation, the Ar‐carrying phase Q became enriched in the metal‐sulfide‐rich chondrule coatings. In the silicate chondrule interior, only the most stable Ne‐carrying presolar diamonds survived the melting event leading to the low observed 36Ar/20Ne ratios. The chondrules studied here do not show evidence for substantial amounts of fractionated solar‐type noble gases from a strong solar wind irradiation of the chondrule precursor material as postulated by others for the chondrules of an enstatite chondrite.  相似文献   
37.
Abstract— Recent results of isotopic dating studies (182Hf‐182W, 26Al‐26Mg) and the increasing number of observed igneous and metamorphosed fragments in (primitive) chondrites provide strong evidence that accretion of differentiated planetesimals predates that of primitive chondrite parent bodies. The primitive chondrites Adrar 003 and Acfer 094 contain some unusual fragments that seem to have undergone recrystallization. Magnesium isotope analyses reveal no detectable radiogenic 26Mg in any of the studied fragments. The possibility that evidence for 26Al was destroyed by parent body metamorphism after formation is not likely because several other constituents of these chondrites do not show any metamorphic features. Since final accretion of a planetesimal must have occurred after formation of its youngest components, formation of these parent bodies must thus have been relatively late (i.e., after most 26Al had decayed). Al‐Mg isotope data for some igneous‐textured clasts (granitoids and andesitic fragments) within the two chondrite regolith breccias Adzhi‐Bogdo and Study Butte reveal also no evidence for radiogenic 26Mg. As calculated from the upper limits, the formation of these igneous clasts, the incorporation into the parent body regolith, and the lithification must have occurred at least 3.8 Myr (andesite in Study Butte) and 4.7 Myr (granitoids in Adzhi‐Bogdo) after calcium‐aluminum‐rich inclusions (CAI) formation. The absence of 26Mg excess in the igneous inclusions does not exclude 26Al from being a heat source for planetary melting. In large, early formed planetesimals, cooling below the closure temperature of the Al‐Mg system may be too late for any evidence for live 26Al (in the form of 26Mg excess) to be preserved. Thus, growing evidence exists that chondritic meteorites represent the products of a complex, multi‐stage history of accretion, parent body modification, disruption and re‐accretion.  相似文献   
38.
Abstract— Depending on their velocity, entry angle and mass, extraterrestrial dust particles suffer certain degrees of heating during entry into Earth's atmosphere, and the mineralogy and chemical composition of these dust particles are significantly changed. In the present study, pulse-heating experiments simulating the atmospheric entry heating of micrometeoroids were carried out in order to understand the mineralogical and chemical changes quantitatively as well as to estimate the peak temperature experienced by the particles during entry heating. Fragments of the CI chondrites Orgueil and Alais as well as pyrrhotites from Orgueil were used as analogue material. The experiments show that the volatile elements S, Zn, Ga, Ge, and Se can be lost from 50 to 100 μm sized CI meteorite fragments at temperatures and heating times applicable to the entry heating of similar sized cosmic dust particles. It is concluded that depletions of these elements relative to CI as observed in micrometeorites are mainly caused by atmospheric entry heating. Besides explaining the element abundances in micrometeorites, the experimentally obtained release patterns can also be used as indicators to estimate the peak heating of dust particles during entry. Using the abundances of Zn and Ge and assuming their original concentrations close to CI, a maximum heating of 1100–1200 °C is obtained for previously analyzed Antarctic micrometeroites. Thermal alteration also strongly influenced the mineralogy of the meteorite fragments. While the unheated samples mainly consisted of phyllosilicates, these phases almost completely transformed into olivine and pyroxene in the fragments heated to ≥800 °C. Therefore, dust particles that still contain hydrous minerals were probably never heated to temperatures ≥800 °C in the atmosphere. During continued heating, the grain size of the newly formed silicates increased and the composition of the olivines equilibrated. Applying these results quantitatively to Antarctic micrometeorites, typical peak temperatures in the range of 1100–1200 °C during atmospheric entry heating are deduced. This temperature range corresponds to the one obtained from the volatile element concentrations measured in these micrometeorites and points to an asteroidal origin of the particles.  相似文献   
39.
Abstract— Rumuruti chondrites (R chondrites) constitute a well‐characterized chondrite group different from carbonaceous, ordinary, and enstatite chondrites. Many of these meteorites are breccias containing primitive type 3 fragments as well as fragments of higher petrologic type. Ca,Al‐rich inclusions (CAIs) occur within all lithologies. Here, we present the results of our search for and analysis of Al‐rich objects in Rumuruti chondrites. We studied 20 R chondrites and found 126 Ca,Al‐rich objects (101 CAIs, 19 Al‐rich chondrules, and 6 spinel‐rich fragments). Based on mineralogical characterization and analysis by SEM and electron microprobe, the inclusions can be grouped into six different types: (1) simple concentric spinel‐rich inclusions (42), (2) fassaite‐rich spherules, (3) complex spinel‐rich CAIs (53), (4) complex diopside‐rich inclusions, (5) Al‐rich chondrules, and (6) Al‐rich (spinel‐rich) fragments. The simple concentric and complex spinel‐rich CAIs have abundant spinel and, based on the presence or absence of different major phases (fassaite, hibonite, Na,Al‐(Cl)‐rich alteration products), can be subdivided into several subgroups. Although there are some similarities between CAIs from R chondrites and inclusions from other chondrite groups with respect to their mineral assemblages, abundance, and size, the overall assemblage of CAIs is distinct to the R‐chondrite group. Some Ca,Al‐rich inclusions appear to be primitive (e.g., low FeO‐contents in spinel, low abundances of Na,Al‐(Cl)‐rich alteration products; abundant perovskite), whereas others were highly altered by nebular and/or parent body processes (e.g., high concentrations of FeO and ZnO in spinel, ilmenite instead of perovskite, abundant Na,Al‐(Cl)‐rich alteration products). There is complete absence of grossite and melilite, which are common in CAIs from most other groups. CAIs from equilibrated R‐chondrite lithologies have abundant secondary Ab‐rich plagioclase (oligoclase) and differ from those in unequilibrated type 3 lithologies which have nepheline and sodalite instead.  相似文献   
40.
Abstract— Calcium, aluminum-rich inclusions (CAIs) are characteristic components in carbonaceous chondrites. Their mineralogy is dominated by refractory oxides and silicates like corundum, perovskite, spinel, hibonite, melilite, and Ca-pyroxene, which are predicted to be the first phases to have condensed from the cooling solar nebula. Allowing insights into processes occurring in the early solar system, CAIs in carbonaceous and ordinary chondrites were studied in great detail, whereas only a few refractory inclusions were found and studied in stratospheric interplanetary dust particles (IDPs) and micrometeorites. This study gives a summary of all previous studies on refractory inclusions in stratospheric IDPs and micrometeorites and will present new data on two Antarctic micrometeorites. The main results are summarized as follows: (a) Eight stratospheric IDPs and six micrometeorites contain Ca, Al-rich inclusions or refractory minerals. The constituent minerals include spinel, perovskite, fassaite, hibonite, melilite, corundum, diopside and anorthite. (b) Four of the seven obtained rare-earth-element (REE) patterns from refractory objects in stratospheric IDPs and micrometeorites are related to Group III patterns known from refractory inclusions from carbonaceous chondrites. A Group II related pattern was found for spinel and perovskite in two micrometeorites. The seventh REE pattern for an orthopyroxene is unique and can be explained by fractionation of Gd, Lu, and Tb at highly reducing conditions. (c) The O-isotopic compositions of most refractory objects in stratospheric IDPs and micrometeorites are similar to those of constituents from carbonaceous chondrites and fall on the carbonaceous chondrites anhydrous minerals mixing line. In fact, in most cases, in terms of mineralogy, REE pattern and O-isotopic composition of refractory inclusions in stratospheric IDPs and micrometeorites are in good agreement with a suggested genetic relation of dust particles and carbonaceous chondrites. Only in the case of one Antarctic micrometeorite does the REE pattern obtained for an orthopyroxene point to a link of this particle to enstatite chondrites.  相似文献   
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