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1.
The D-CIXS Compact X-ray Spectrometer will provide high quality spectroscopic mapping of the Moon, the primary science target of the ESA SMART-1 mission. D-CIXS consists of a high throughput spectrometer, which will perform spatially localised X-ray fluorescence spectroscopy. It will also carry a solar monitor, to provide the direct calibration needed to produce a global map of absolute lunar elemental abundances, the first time this has been done. Thus it will achieve ground breaking science within a resource envelope far smaller than previously thought possible for this type of instrument, by exploiting two new technologies, swept charge devices and micro-structure collimators. The new technology does not require cold running, with its associated overheads to the spacecraft. At the same time it will demonstrate a radically novel approach to building a type of instrument essential for the BepiColombo mission and potential future planetary science targets.  相似文献   
2.
《Cretaceous Research》2008,29(1):87-99
The first carbon and oxygen isotope curves for the Valanginian to Early Barremian (Early Cretaceous) interval obtained from outcrops in the Southern Hemisphere are presented. They were obtained from well-dated (by ammonites) sediments from the Neuquén Basin, Argentina. Measurements were acquired by the innovative method of analysing fossil oyster laminae. The occurrence of the well-established mid-Valanginian positive carbon isotope excursion is documented, while less well-marked positive events may also correlate with peaks identified in the well-known successions of SE France. The mid-Valanginian positive carbon isotope event in the Neuquén Basin is possibly associated with organic-rich sediments. A similar relationship is seen in the European Alps and in oceanic cores in some areas of the world.  相似文献   
3.
The sulfur isotopic composition of carbonate associated sulfate (CAS) has been used to investigate the geochemistry of ancient seawater sulfate. However, few studies have quantified the reliability of δ34S of CAS as a seawater sulfate proxy, especially with respect to later diagenetic overprinting. Pyrite, which typically has depleted δ34S values due to authigenic fractionation associated with bacterial sulfate reduction, is a common constituent of marine sedimentary rocks. The oxidation of pyrite, whether during diagenesis or sample preparation, could thus adversely influence the sulfur isotopic composition of CAS. Here, we report the results of CAS extractions using HCl and acetic acid with samples spiked with varying amounts of pyrite. The results show a very strong linear relationship between the abundance of fine-grained pyrite added to the sample and the resultant abundance and δ34S value of CAS. This data represents the first unequivocal evidence that pyrite is oxidized during the CAS extraction process. Our mixing models indicate that in samples with much less than 1 wt.% pyrite and relatively high δ34Spyrite values, the isotopic offset imparted by oxidation of pyrite should be much less than ? 4‰. A wealth of literature exists on the oxidation of pyrite by Fe3+ and we believe this mechanism drives the oxidation of pyrite during CAS extraction, during which the oxygen used to form sulfate is taken from H2O, not O2. Consequently, extracting CAS under anaerobic conditions would only slow, but not halt, the oxidation of pyrite. Future studies of CAS should attempt to quantify pyrite abundance and isotopic composition.  相似文献   
4.
《Chemical Geology》2006,225(1-2):30-39
The discovery of mass-independent isotope effects observed in Archean rocks, certain classes of meteorites, and atmospheric aerosols has had profound implications to our understanding of ancient and present atmospheric sulfur chemistry. We present a new technique that takes advantage of continuous He flow isotope-ratio-monitoring gas chromatography–mass spectrometry to achieve precise analysis of all four stable sulfur isotopes (32S, 33S, 34S, and 36S) at nanomole level samples. The technique involves fluorination of sulfide (silver sulfide or pyrite), and separation of product gas by gas chromatography and the removal of mass-131 interference by a liquid-nitrogen ethanol slush at − 110 °C. This technique works with an optimum sample size of 100 to 200 nmol with precision for Δ33S and Δ36S at 0.1 and 0.5‰ (2σ). Samples, as small as tens of nanomole, can be analyzed using this new method. One of the major sources of error in irm-GCMS is found to be tailing of the major ion beam (32SF5+) onto minor beams (33SF5+ and 36SF5+), which results in contraction of the measured δ33S and δ36S scales. This effect is corrected by measuring a series of reference sulfide samples with mass-dependent sulfur isotope compositions. This methodology increases the spatial resolution of the laser ablation in situ analysis and considerably reduces the analysis time as compared with conventional dual inlet methods.  相似文献   
5.
《Applied Geochemistry》2006,21(5):813-819
An alternative IR microscopy system in the NIR (near infrared, up to 10 μm) and SWIR (short wavelength infrared, up to 1.4 μm) ranges has been developed for the study of opaque ore minerals. The system uses either IR LED or IR light bulb sources depending on the degree of opacity of the investigated minerals. This paper presents the methodology and the promising results obtained in studies of opaque ore minerals such as Ag minerals (pyrargyrite) from epithermal deposits and Nb-tantalates (columbite) from pegmatites. It also presents results on the internal features of hematites from Fe ore banded formations and tungstates from granite–greenstone belt deposits. The data obtained on fluid inclusions from pyrargyrite and hematite crystals have been integrated by complementary information from X-ray fluorescence analysis using synchrotron radiation (μ-SXRF) under conditions specifically designed for the study of opaque ore minerals.  相似文献   
6.
《Applied Geochemistry》2006,21(7):1169-1183
The Cornia Plain alluvial aquifer, in Tuscany, is exploited intensely to meet the demand for domestic, irrigation and industrial water supplies. The B concentration of groundwater, however, is often above the European limit of 1 mg L−1, with the result that exploitation of these water resources requires careful management. Boron and Sr isotopes have been used as part of a study on the origin and distribution of B dissolved in groundwater, and indirectly as a contribution to the development of appropriate water management strategies.The geochemistry of the Cornia Plain groundwater changes from a HCO3 facies in the inland areas to a Cl facies along the coastal belt, where seawater intrusion takes place. The B concentration of groundwater increases towards the coastal areas, while the 11B/10B ratio decreases. This indicates that there is an increasing interaction between dissolved B and the sediments forming the aquifer matrix, whose B content is in the order of 100 mg kg−1. Adsorption–desorption exchanges take place between water and the sediment fine fraction rich in clay minerals, with a net release of B from the matrix into the groundwater, and a consequent δ11B shift from positive to negative values. The aquifer matrix sediments therefore seem to be the major source of B dissolved in the groundwater.The groundwater–matrix interactions triggered by the ionic strength increase caused by seawater intrusion can also be detected in the Ca–Na ion exchanges. Dissolved Sr follows a trend similar to that of Ca, while the 87Sr/86Sr ratio is equal to that of the exchangeable Sr of the aquifer matrix and therefore does not change significantly.These results have helped to define a new strategy for groundwater exploitation, with the final objective of reducing B concentration in the water extracted from the aquifer.  相似文献   
7.
Water-soluble sulfate salts extracted from six CM chondrites have oxygen isotope compositions that are consistent with an extraterrestrial origin. The Δ17O of sulfate are correlated with previously reported whole rock δ18O and with an index of meteorite alteration, and may display a correlation with the date of the fall. The enrichments and depletions for Δ17O of water-soluble sulfate from the CM chondrites relative to the terrestrial mass dependent fractionation line are consistent with sulfate formation in a rock dominated asteroidal environment, and from aqueous fluids that had undergone relatively low amounts of oxygen isotope exchange and little reaction with anhydrous components of the meteorites. It is unresolved how the oxidation of sulfide to sulfate can be reconciled with the inferred low oxidation state during the extraterrestrial alteration process. Oxygen isotope data for two CI chondrites, Orgueil and Ivuna, as well as the ungrouped C2 chondrite Essebi are indistinguishable from sulfate of terrestrial origin and may be terrestrial weathering products, consistent with previous assertions. Our oxygen isotope data, however, can not rule out a preterrestrial origin either.  相似文献   
8.
《Quaternary Science Reviews》2005,24(14-15):1673-1690
Sedimentary sequences deposited by the decaying marine margin of the British–Irish Ice Sheet (BIIS) record isostatic depression and successive ice sheet retreat towards centres of ice dispersion. Radiocarbon dating by accelerator mass spectrometry (AMS) of in situ marine microfaunas that are commonly associated with these sequences constrain the timing of glacial and sea level fluctuations during the last deglaciation, enabling us to evaluate the dynamics of the BIIS and its response to North Atlantic climate change. Here we use our radiocarbon-dated stratigraphy to define six major glacial and sea level events since the Last Glacial Maximum. (1) Initial deglaciation may have occurred ⩾18.3 kyr 14C BP along the northwestern Irish coast, in agreement with a deglacial age of ∼22 36Cl kyr BP for southwestern Ireland. Ice retreated to inland centres and areas of transverse moraine began to form across the north Irish lowlands. (2) Channels cut into glaciomarine deglacial sediments along the western Irish Sea coast are graded to below present sea level, identifying a fall of relative sea level (RSL) in response to isostatic emergence of the coast. (3) Marine mud that rapidly infilled these channels records an abrupt rise in global sea level of 10–15 m ∼16.7 14C kyr BP that flooded the Irish Sea coast and may have triggered deglaciation of a marine-based margin in Donegal Bay. (4) Intertidal boulder pavements in Dundalk Bay indicate that RSL ∼15.0 14C kyr BP was similar to present. (5) A major readvance of all sectors of the BIIS occurred between 14 and 15 kyr 14C BP which overprinted subglacial transverse moraines and delivered a substantial sediment flux to tidewater ice sheet margins. This event, the Killard Point Stadial, indicates that the BIIS participated in Heinrich event 1. (6) Subsequent deposition of marine muds on drumlins 12.7 14C kyr BP indicates isostatic depression and attendant high RSL resulting from the Killard Point readvance. These events identify a dynamic BIIS during the last deglaciation, as well as significant changes in RSL that reflect a combination of isostatic loading and eustatic changes in global sea level.  相似文献   
9.
This work provides five new U–Pb zircon dating and the corresponding Nd isotope data for felsic granulites from the south Itabuna-Salvador-Curaçá Block (ISCB), in the São Francisco Craton, Brazil. Three major sets of felsic granulites can be recognised. The oldest set is tonalitic in composition and of TTG affinity. It is Archaean in age with magmatic zircon cores dated at 2675 ± 11 Ma by LA-ICPMS and up to ca 2.7–2.9 Ga by SHRIMP on an other sample. It exhibits epsilon Nd values between ?8 and ?11 at 2.1 Ga. This Nd signature is similar to that of granulites found in the western Archaean Jequié Block. Cartographically, this set of Archaean terrains represents at least 50% of the granulites in the studied area. The second set corresponds to a Palaeoproterozoic calc-alkaline tonalitic suite with zircon ages from 2019 ± 19 Ma to 2191 ± 10 Ma and epsilon Nd values between ?3 and ?4 at 2.1 Ga, corresponding partially to a newly formed crust. The third set of granulites is also Palaeoproterozoic. It is shoshonitic to monzonitic in composition and synchronous with the high grade metamorphism dated by metamorphic zircons at 2086 ± 7 Ma (average of five samples). The Nd isotope signature for this alkaline set is similar to that of the Palaeoproterozoic calc-alkaline one. Nd isotopes appear to be a very efficient tool to distinguish Archaean from Palaeoproterozoic felsic protoliths in granulitic suites of the Itabuna-Salvador-Curaçá Block (ISCB). Finally, the southern part of the ISCB is composed of a mixture of Archaean and Palaeoproterozoic protoliths, in similar amounts, suggesting that it was probably an active margin between 2.1 and 2.2 Ga located on the eastern border of the Archaean Jequié Block. A major crustal thickening process occurred at ca 2.09 Ga in the ISCB and seems significantly younger towards the west, in the Jequié granulites, where an average of 2056 ± 9 Ma is determined for the high grade event.  相似文献   
10.
Southeastern Papua New Guinea has hosted magmatism throughout the Cenozoic, with the latest phase being concurrent with active extension in the Woodlark Rift. There, the Suckling-Dayman metamorphic core complex (SDMCC) has exhumed middle-crustal rocks in the past few million years along a still-active low-angle normal fault, the Mai'iu Fault. Uplift of the SDMCC has exposed metasedimentary and metaigneous rocks of Late Cretaceous-Pleistocene age that record an evolution from oceanic spreading to subduction, to collision, and finally to subduction-inversion and extensional exhumation. We present new petrographic, whole-rock geochemical and geochronologic (zircon U–Pb LA-ICP-MS) data from the SDMCC to reconstruct its long-term evolution. The dominant footwall-lithology of the SDMCC, the Goropu Metabasalt, has a MORB composition. Detrital zircons from metasedimentary beds intercalated with these basalts yield U–Pb-based maximum estimates for deposition of ~103 and ~72 Ma, suggesting a Late Cretaceous spreading age of the oceanic protolith. Bulk compositions of low-grade tholeiitic meta-gabbroic and -tonalitic rocks (Yau Igneous Complex) that intrude the Goropu Metabasalt reveal both enriched and depleted light rare earth element patterns. Zircon U–Pb ages from the Yau Igneous Complex range between ~60 and ~57 Ma, providing a minimum age for the formation of the Goropu Metabasalt. Much younger syn-extensional granitoids in the mafic footwall of the SDMCC have calc-alkaline to high-K compositions and U–Pb ages on zircon between ~3.7 and ~2.0 Ma. Our data indicate that the Mai'iu Fault had re-activated a Paleogene thrust as an extensional detachment fault by 3.7 ± 0.2 Ma. U–Pb ages of detrital zircons in modern streams draining the footwall of the SDMCC essentially reflect the ages revealed by the Paleocene and Plio-Pleistocene intrusions. Xenocrystic zircons in the Plio-Pleistocene granitoids imply that the crust underlying the metabasaltic carapace of the SDMCC consists chiefly of Australian-continent derived sedimentary rocks.  相似文献   
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