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61.
Stable isotopes and trace elements in ostracod shells have been used widely in paleolimnological investigations of past lake hydrochemistry and climate because they provide insights into past water balance and solute evolution of lakes. Regional differences in lake characteristics and species-specific element fractionation, however, do not permit generalization of results from other regions or ostracod species to the southern Tibetan Plateau, in part because most common taxa from the southern Tibetan Plateau are endemic to the area. This study evaluated relations between present-day environmental conditions and the geochemical composition of modern ostracod shells from the southern Tibetan Plateau, to assess the suitability of using shell chemistry to infer hydrological conditions. We studied nine lakes and their catchments, located along a west–east transect in the south-central part of the Tibetan Plateau. Stable oxygen and carbon isotope values and trace element concentrations in recent shells from the four most abundant ostracod species (Leucocytherella sinensis, ?Leucocythere dorsotuberosa, Limnocythere inopinata, Tonnacypris gyirongensis) were measured, together with hydrochemical properties of host waters at the time of sampling. Results revealed significant between-species differences in stable isotope fractionation and trace element incorporation into shell calcite. Stable oxygen and carbon isotope values of ostracod shells were correlated significantly with the stable isotope composition of the respective water body \( \left( {\updelta^{18} {\text{O}}_{{{\text{H}}_{ 2} {\text{O}}}} \,{\text{and }}\updelta^{13} {\text{C}}_{{{\text{H}}_{ 2} {\text{O}}}} } \right) \), reflecting salinity and productivity, respectively. Offsets between δ18Oshell and δ13Cshell and inorganic calcite, the latter representing isotopic equilibrium, suggest shell formation of T. gyirongensis during spring melt. L. sinensis reproduces throughout the monsoon season until September and shows several consecutive generations, and L. inopinata molts to the adult stage after the monsoon season in August/September. The influence of pore water δ13C was displayed by L. inopinata, suggesting shell calcification within the sediment. Mg/Cashell is primarily influenced by water Mg/Ca ratios and salinity and confirms the use of this shell ratio as a proxy for precipitation-evaporation balance and lake level. In addition, Sr/Ca and Ba/Ca can be used to infer changes in salinity, at least in closed-basin lakes with calcite saturation. Observed effects of water Sr/Ca and salinity on Sr/Ca incorporation are biased by the presence of aragonite precipitation in the lakes, which removes bioavailable Sr from the host water, resulting in low Sr/Cashell values. Changes in carbonate mineralogy affect the bioavailability of trace elements, a process that should be considered in paleoclimate reconstructions. Oxygen isotopes and Mg/Cashell ratios were unaffected by water temperature. Positive correlations among Fe/Ca, Mn/Ca and U/Ca in ostracod shells, and their negative correlation with δ13C, which reflects organic matter decay, show the potential to infer changes in redox conditions that can be used to reconstruct past oxygen supply to bottom waters and thus past water-circulation changes within lakes. The intensity of microbial activity, associated with organic matter decomposition, can be inferred from U/Ca ratios in ostracod shells. These findings highlight the value of fossil ostracod records in lake deposits for inferring paleoenvironmental conditions on the southern Tibetan Plateau.  相似文献   
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Understanding the degree of sea/saltwater intrusion in coastal regions is of great significance to treating the intrusion and improving the environment. Based on the character analysis of the sea/saltwater intrusion, five factors were selected in the fuzzy-synthetical evaluation approach to form the index system, so as to evaluate the degree of sea/saltwater intrusion in southern Laizhou Bay. The results show that the sea/saltwater intrusion is stronger in the middle and northern areas and weaker on the sides and in southern area; currently, the intrusion is relatively serious, and the intrusion area has covered about 68.2% of the areas under study, among which the heavily intruded area is over 50%. Based on the factors analysis of the occurrence and development of sea/saltwater intrusion, the thesis proposes treatment measures.  相似文献   
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Abstract— Two rare, spinel-bearing, Al-rich chondrules have been identified in new chondrite finds from Roosevelt County, New Mexico—RC 071 (L4) and RC 072 (L5). These chondrules have unusual mineralogies, dominated by highly and asymmetrically zoned, Al-Cr-rich spinels. Two alternatives exist to explain the origin of this zoning—fractional crystallization or metamorphism. It appears that fractional crystallization formed the zoning of the trivalent cations (Al, Cr) and caused a localized depletion in chromites around the large Al-Cr-rich spinels. The origin of the zoning of the divalent cations (Fe, Mg, Zn) is less certain. Diffusive exchange and partitioning of Fe and Mg between olivine and spinel during parent body metamorphism can explain the asymmetric zoning of these elements. Unfortunately, appropriate studies of natural and experimental systems to evaluate the formation of zoning of the divalent cations by fractional crystallization have not yet been conducted. The bulk compositions of the chondrules suggest affinities with the Na-Al-Cr-rich chondrules, as would be expected from the abundance of Al-Cr-rich spinels. Melting of rare and unusual precursors produced the compositions of Na-Al-Cr-rich chondrules, possibly including a spinel-rich precursor enriched in Cr2O3 and ZnO. The two chondrules we studied have larger modal abundances of Al-Cr-rich spinels than reported in other Na-Al-Cr-rich chondrules of similar composition, and Al-rich chondrules even more enriched in spinel are reported in the literature. These differences indicate that factors other than bulk composition control the mineralogy of the chondrules. The most important of these factors are the temperature to which the molten chondrule was heated and the cooling rate during crystallization. These two chondrules cooled rapidly from near the liquidus, as indicated by the zoning, occurrence and sizes of spinels, radiating chondrule textures and localized chromite depletions. The range of mineralogies in other Al-rich chondrules of similar composition reflect a range of peak temperatures and cooling rates. We see no reason to believe that this range is fundamentally different from the range of thermal histories experienced by “normal” Fe-Mg-rich chondrules.  相似文献   
66.
The Adams County, Colorado, H5 chondrite contains a lithic fragment, 1 cm in size, that is texturally and mineralogically quite different from the chondritic host. It is composed of: a groundmass of fine-grained euhedral to subhedral olivine (3–15 μm) and interstitial glass enclosing larger olivine and pyroxene grains (0.15-0.5 mm; about 15 vol %); an assemblage of enstatite grains (subfragment within) and an assemblage of olivine plus orthopyroxene (a second subfragment); and about 11 vol % grains of mixed troilite and nickel-iron metal. Analyses yielded these results: (i) olivine grains of the fragment groundmass have a compositional range (Fa12–45) and most grains contain substantial CaO and Cr2O3 (~ 0.20 and 0.30 avg. wt%, respectively); interstitial glass has ~ 55 wt% SiO2; (ii) larger olivine grains of the fragment are similarly high in CaO and Cr2O3 and also have a wide FeO/MgO range; one unusual pyroxene is an Mg-rich pigeonite; (iii) the metal is martensite in composition (11–14 wt% Ni); and (iv) major and trace element analyses by INAA indicate an H-group bulk composition for the entire 1 cm lithic fragment. On the basis of its texture and bulk and mineral compositions, the fragment is interpreted to represent unequilibrated H-group material that was partly melted by impact. The Ca- and Cr-enriched groundmass olivine and interstitial glass resulted from rapid crystallization of the chondritic melt. The Ca- and Cr-enriched larger silicate grains, including the enstatite sub-fragment and the pigeonite grain, are residual, unmelted clasts from the target material (this is supported by the presence of similar material in actual H3 chondrites). Further impact brecciation of the clast-laden melt material, and resultant impact-splashing accounts for the presence of the fragment in the H-group Adams County host and documents the coexistence of unequilibrated and equilibrated H-group material as surface regolith on one parent body.  相似文献   
67.
The stability of the solar wind is studied in the case of spherical symmetry and constant temperature. It is shown that the stability problem must be formulated as a mixed initial and boundary-value problem in which are prescribed the perturbation values of velocity and density at an initial time and additionally the velocity perturbation at the base of the corona for all times. The solution is constructed by linear superposition of normal solutions, which contain the time only in an exponential factor. The stability problem becomes a singular eigenvalue problem for the amplitudes of the velocity and pressure perturbations, since additionally to the boundary condition at the base of the corona one must add the condition that the amplitudes behave regularly at the critical point. It is proved that only stable eigenvalues exist.  相似文献   
68.
A total of 150 samples were collected at a 10-days' anchor station in the Bornholm basin (55° 31.1′N, 15° 32.1′E) and analyzed for dissolved (< 0.4 μm) and particulate trace metals. For dissolved Mn, large gradients have been found in the vertical distribution with minimum concentrations (< 0.2 μgl?1) in the halocline zone and considerably higher values in the deep waters (up to 50 μgl?1). Ultrafiltration studies indicate that dissolved Mn is probably present as Mn2+ in the oxygenated bottom layer. The primary production process was not evident in the particulate Mn profile; the suspended particulate material (SPM), however, shows a considerable enrichment with depth, apparently due to Mn-oxide precipitation.The distribution of dissolved Fe was rather homogeneous, with average concentrations throughout the water column between 0.86 and 1.1 μgl?1, indicating that the oxidation of Fe2+ ions released from the sediments must already be complete in the very near oxidation boundary layer. Relatively high concentrations of particulate Fe were actually measured in the bottom layer, with the maximum mean of 11.2 μgl?1 at 72 m. Similarly to Mn, the profile of particulate Fe does not reflect the SPM curve of the eutrophic layer. On average, about 70% of the total Fe in surface waters was found to be particulate.The average concentrations of dissolved Zn, Cd and Cu were found to be rather homogeneous in the water column but showed a relatively high variability with time. A simplified model on trace-metal uptake by phytoplankton indicates no significant change in dissolved metal concentrations during the period of investigation. On average, only 1.7% Zn, 3.3% Cd and 9.8% Cu of the total metal concentrations were found in particulate form. SPM analyses showed significant correlations of Zn, Cd and Cu with Fe, indicating that particulate iron is an important carrier for particulate trace metals in Baltic waters.  相似文献   
69.
Rock 12039 belongs to the olivine-depleted group of magmatic rocks characterized by normative and modal SiO2, absence or very low abundance of olivine, and high FeO/(FeO + MgO), Ti/Cr, and CaO/MgO ratios. Clinopyroxenes in this rock show a complex, essentially continuous, compositional zonation from augite cores through ferroaugite to ferrohedenbergite with an abrupt discontinuity at the pyroxferroite contact and, thus, are different from pyroxene in most other Apollo 12 rocks. Two grains contain thin subcalcic pigeonite zones. Texture, presence of very fine (< 1 μm) exsolution lamallae, and pyroxene zoning indicate a relatively rapid cooling history and pronounced in situ chemical fractionation. Rock 12039, on the basis of mineralogy and bulk composition, is the most highly differentiated member of the olivine-depleted basalt group  相似文献   
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