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The Sutter's Mill (SM) meteorite fell in El Dorado County, California, on April 22, 2012. This meteorite is a regolith breccia composed of CM chondrite material and at least one xenolithic phase: oldhamite. The meteorite studied here, SM2 (subsample 5), was one of three meteorites collected before it rained extensively on the debris site, thus preserving the original asteroid regolith mineralogy. Two relatively large (10 μm sized) possible diamond grains were observed in SM2‐5 surrounded by fine‐grained matrix. In the present work, we analyzed a focused ion beam (FIB) milled thin section that transected a region containing these two potential diamond grains as well as the surrounding fine‐grained matrix employing carbon and nitrogen X‐ray absorption near‐edge structure (C‐XANES and N‐XANES) spectroscopy using a scanning transmission X‐ray microscope (STXM) (Beamline 5.3.2 at the Advanced Light Source, Lawrence Berkeley National Laboratory). The STXM analysis revealed that the matrix of SM2‐5 contains C‐rich grains, possibly organic nanoglobules. A single carbonate grain was also detected. The C‐XANES spectrum of the matrix is similar to that of insoluble organic matter (IOM) found in other CM chondrites. However, no significant nitrogen‐bearing functional groups were observed with N‐XANES. One of the possible diamond grains contains a Ca‐bearing inclusion that is not carbonate. C‐XANES features of the diamond‐edges suggest that the diamond might have formed by the CVD process, or in a high‐temperature and ‐pressure environment in the interior of a much larger parent body.  相似文献   
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A Re–Os isochron age is reported for massive sulfides from near the basal contact of the Radio Hill layered mafic‐ultramafic intrusion in the west Pilbara Craton, Western Australia. The isochron age is 2892 ± 34 Ma (mean square of weighted deviates = 1.06) with an initial 187Os/188Os = 0.1265 ± 0.0028. This age is in agreement with the ages of other nearby layered mafic intrusions that are considered to have a similar geological evolution to the Radio Hill Intrusion.  相似文献   
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The solubility and solution mechanisms of reduced COH volatiles in Na2OSiO2 melts in equilibrium with a (H2 + CH4) fluid at the hydrogen fugacity defined by the iron-wüstite + H2O buffer [fH2(IW)] have been determined as a function of pressure (1-2.5 GPa) and silicate melt polymerization (NBO/Si: nonbridging oxygen per silicon) at 1400 °C. The solubility, calculated as CH4, increases from ∼0.2 wt% to ∼0.5 wt% in the melt NBO/Si-range ∼0.4 to ∼1.0. The solubility is not significantly pressure-dependent, probably because fH2(IW) in the 1-2.5 GPa range does not vary greatly with pressure. Carbon isotope fractionation between methane-saturated melts and (H2 + CH4) fluid varied by ∼14‰ in the NBO/Si-range of these melts.The (C..H) and (O..H) speciation in the quenched melts was determined with Raman and 1H MAS NMR spectroscopy. The dominant (C..H)-bearing complexes are molecular methane, CH4, and a complex or functional group that includes entities with CCH bonding. Minor abundance of complexes that include SiOCH3 bonding is tentatively identified in some melts. There is no spectroscopic evidence for SiC or SiCH3. Raman spectra indicate silicate melt depolymerization (increasing NBO/Si). The [CH4/CCH]melt abundance ratio is positively correlated with NBO/Si, which is interpreted to suggest that the (CCH)-containing structural entity is bonded to the silicate melt network structure via its nonbridging oxygen. The ∼14‰ carbon isotope fractionation change between fluid and melt is because of the speciation changes of carbon in the melt.  相似文献   
25.
We present new reference values for the NIST SRM 610–617 glasses following ISO guidelines and the International Association of Geoanalysts’ protocol. Uncertainties at the 95% confidence level (CL) have been determined for bulk‐ and micro‐analytical purposes. In contrast to former compilation procedures, this approach delivers data that consider present‐day requirements of data quality. New analytical data and the nearly complete data set of the GeoReM database were used for this study. Data quality was checked by the application of the Horwitz function and by a careful investigation of analytical procedures. We have determined quantitatively possible element inhomogeneities using different test portion masses of 1, 0.1 and 0.02 μg. Although avoiding the rim region of the glass wafers, we found moderate inhomogeneities of several chalcophile/siderophile elements and gross inhomogeneities of Ni, Se, Pd and Pt at small test portion masses. The extent of inhomogeneity was included in the determination of uncertainties. While the new reference values agree with the NIST certified values with the one exception of Mn in SRM 610, they typically differ by as much as 10% from the Pearce et al. (1997) values in current use. In a few cases (P, S, Cl, Ta, Re) the discrepancies are even higher.  相似文献   
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Concentration‐discharge (c‐Q) plots are routinely used as an integrated signal of watershed response to infer solute sources and travel pathways. However, the interpretation of c‐Q data can be difficult unless these data are fitted using statistical models. Such models are frequently applied for geogenic solutes, but it is unclear to what extent they might aid in the investigation of nutrient export patterns, particularly for total dissolved phosphorus (TDP) which is a critical driver of downstream eutrophication problems. The goal of the present study was therefore to statistically model c‐Q relations (where c is TDP concentrations) in a set of contrasting watersheds in the Northern Great Plains—ranging in size from 0.2 to 1000+ km2—to assess the controls of landscape properties on TDP transport dynamics. Six statistical models were fitted to c‐Q data, notably (a) one linear model, (b) one model assuming that c‐Q relations are driven by the mixing of end‐member waters from different landscape locations (i.e., hydrograph separation), (c) one model relying on a biogeochemical stationarity hypothesis (i.e., power law), (d) one model hypothesizing that c‐Q relations change as a function of the solute subsurface contact time (i.e., hyperbolic model), and (e) two models assuming that solute fluxes are mostly dependent on reaction rates (i.e., chemical models). Model performance ranged from mediocre (R2 < 0.2) to very good (R2 > 0.9), but the hydrograph separation model seemed most universal. No watershed was found to exhibit chemostatic behaviour, but many showed signs of dilution or enrichment behaviour. A tendency toward a multi‐model fit and better model performance was observed for watersheds with moderate slope and higher effective drainage area. The relatively poor model performance obtained outside these conditions illustrates the likely importance of controls on TDP concentrations in the region that are independent of flow dynamics.  相似文献   
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Here, we present the results of a multitechnique study of the bulk properties of insoluble organic material (IOM) from the Tagish Lake meteorite, including four lithologies that have undergone different degrees of aqueous alteration. The IOM C contents of all four lithologies are very uniform and comprise about half the bulk C and N contents of the lithologies. However, the bulk IOM elemental and isotopic compositions vary significantly. In particular, there is a correlated decrease in bulk IOM H/C ratios and δD values with increasing degree of alteration—the IOM in the least altered lithology is intermediate between CM and CR IOM, while that in the more altered lithologies resembles the very aromatic IOM in mildly metamorphosed CV and CO chondrites, and heated CMs. Nuclear magnetic resonance (NMR) spectroscopy, C X‐ray absorption near‐edge (XANES), and Fourier transform infrared (FTIR) spectroscopy confirm and quantitate this transformation from CR‐like, relatively aliphatic IOM functional group chemistry to a highly aromatic one. The transformation is almost certainly thermally driven, and probably occurred under hydrothermal conditions. The lack of a paramagnetic shift in 13C NMR spectra and 1s‐σ* exciton in the C‐XANES spectra, both typically seen in metamorphosed chondrites, shows that the temperatures were lower and/or the timescales were shorter than experienced by even the least metamorphosed type 3 chondrites. Two endmember models were considered to quantitatively account for the changes in IOM functional group chemistry, but the one in which the transformations involved quantitative conversion of aliphatic material to aromatic material was the more successful. It seems likely that similar processes were involved in producing the diversity of IOM compositions and functional group chemistries among CR, CM, and CI chondrites. If correct, CRs experienced the lowest temperatures, while CM and CI chondrites experienced similar more elevated temperatures. This ordering is inconsistent with alteration temperatures based on mineralogy and O isotopes.  相似文献   
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We present intermediate-resolution spectroscopic data for a set of dwarf and giant galaxies in the Coma cluster, with  −20.6 < MR < −15.7.  The photometric and kinematic properties of the brighter galaxies can be cast in terms of parameters which present little scatter with respect to a set of scaling relations known as the fundamental plane. To determine the form of these fundamental scaling relations at lower luminosities, we have measured velocity dispersions for a sample comprising 69 galaxies on the border of the dwarf and giant regime. Combining these data with our photometric survey, we find a tight correlation of luminosity and velocity dispersion,   L ∝σ2.0  , substantially flatter than the Faber–Jackson relation characterizing giant elliptical galaxies. In addition, the variation of mass-to-light ( M / L ) ratio with velocity dispersion is quite weak in our dwarf sample:   M / L ∝σ0.2.  Our overall results are consistent with theoretical models invoking large-scale mass removal and subsequent structural readjustment, e.g. as a result of galactic winds.  相似文献   
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