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21.
During recent years laboratory studies have demonstrated the presence of metallothionein in several species of teleosts.1–3 The role of metallothionein (MT) in protection against cadmium toxicity has been investigated by exposing fish to high levels of cadmium in the water.4–6 So far, however, few field studies have focused on the existence of MT and its role in subcellular distribution of cadmium.7 In the present study the synthesis of MT as a possible mechanism by which perch adapt to cadmium contamination was investigated in a wild population of perch. An increased MT content of perch liver was found to correlate to an increase in cadmium present in the liver.  相似文献   
22.
The concentrations of total carbonate (Ct), sulphate, sulphide, thiols and oxygen, the ratio between the stable sulphur isotopes 34S and 32S in sulphate and sulphide, and the density (used to calculate salinity) were determined on samples from the water column of Framvaren, a superanoxic fjord in southern Norway. From a depth of 18m (the oxic-anoxic boundary) the initial sulphate concentration, ([SO4]init), as calculated from salinity, is significantly higher than the sum of the measured sulphur species. This is attributed to a loss of sulphur from the water column. The amount of total carbonate produced, corrected for the initial concentration (Ct - 2.4 Sal/35) is found to be proportional to the amount of sulphate consumed, ([SO4]init - [SO4]), according to the following relation Ct- 2.4 Sal/35 = 1.84 ([SO4]init - [SO4]). Isotopic fractionation caused by bacterial sulphate reduction in the anoxic part of the water column produces sulphide with a δ34S 40‰ lower than the δ34S for sulphate at corresponding depths. The isotopic fractionation also results in δ34S value for the remaining sulphate at depths below 80 m being considerably higher than the mean value for ocean water, which is close to + 20‰. The δ34S values for sulphate at depths between 10 and 50 m were lower than + 20‰ which indicates oxidation of sulphide, which follows upon diffusion of sulphide from deeper parts of the water column and inflow of oxygenated seawater over the sill into the anoxic water of the fjord. A conclusive scenario of the Framvaren sulphur chemistry is presented.  相似文献   
23.
This environmental overview of Eckernförde Bay (northern Germany) summarizes the results of previous studies relevant to the Office of Naval Research's Coastal Benthic Boundary Layer (CBBL) Baltic field exercise conducted during 1993–1994. Significant environmental characteristics include the following: (1) surface sediment distribution is related to water depth, dictated primarily by hydrodynamic reworking of older glacial deposits; (2) the origin and characteristics of small-scale sedimentary structures depend on storm-generated waves and currents; (3) the proximity of the sea surface and sediment —water interface results in a pelagic—benthic coupling that drives biogeochemical processes and produces organicrich, acoustically turbid sediments; and (4) the bay floor is complicated topographically by pockmarks and manmade sedimentary structures.  相似文献   
24.
A theoretical and an experimental investigation was carried out, where a carbon fibre corrugated circular cylinder was tested to destuction under external hydrostatic pressure. The theoretical investigation was via the finite element method, where the structure was modelled with several orthotropic axisymmetric thin-walled shell elements. The experimental observations were aided with strategically placed strain gauges. Comparison between theory and experiment showed that the experimentally observed buckling pressure was a little lower than the theoretical prediction. This may have been due to the fact that the model had slight initial geometrical imperfections in the circumferenential direction.  相似文献   
25.
26.
Historical data of total dissolved inorganic carbon (CT), together with nitrate and phosphate, have been used to model the evolution of these constituents over the year in the Atlantic water of the Norwegian Sea. Changes in nutrient concentration in the upper layer of the ocean are largely related to biological activity, but vertical mixing with the underlying water will also have an impact. A mixing factor is estimated and used to compute the entrainment of these constituents into the surface water from below. After taking the mixing contribution into account, the resulting nutrient concentration changes are attributed to biological production or decay. The results of the model show that the change in CT by vertical mixing and by biological activity based on nutrient equivalents needs another sink to balance the carbon budget. It cannot be the atmosphere as the surface water is undersaturated with respect to carbon dioxide and is, thus, a source of CT in this region. Inasmuch as the peak deficit of carbon is more than a month later than for the nutrients, the most plausible explanation is that other nitrogen and phosphate sources than the inorganic salts are used together with dissolved inorganic carbon during this period. As nitrate and phosphate show a similar trend, it is unlikely that the explanation is the use of ammonia or nitrogen fixation but rather dissolved organic nitrogen and phosphate, while dissolved organic carbon is accumulating in the water.  相似文献   
27.
The paper describes experimental tests carried out on three ring-stiffened cones that were tested to destruction under external hydrostatic pressure. The cones were carefully machined from EN1A Steel. All three cones failed by plastic non-symmetric bifurcation buckling in a mode commonly known as general instability. In this mode the entire ring-shell combination buckles bodily.The paper also provides a design chart using the results obtained from these three vessels, together with the results of six other vessels obtained from other tests. The design chart allows the possibility of obtaining a plastic knock down factor, so that the theoretical buckling pressures, based on elastic theory, can be divided by the plastic knockdown factor, to give the predicted buckling pressure. This method can also be used for the design of full-scale vessels.  相似文献   
28.
29.
The long-period tides are a tool for understanding oceanic motions at low frequencies and large scales. Here we review observations and theory of the fortnightly, monthly and pole tide constitutents. Observations have been plagued by low signal-to-noise ratios and theory by the complex lateral geometry and great sensitivity to bottom slopes. A new spectral element model is used to compute the oceanic response to tidal forcing at 2-week and monthly periods. The general response is that of a heavily damped (Q ≈ 5) system with both the energy input from the moon and the dissipation strongly localized in space. The high dissipation result is probably generally applicable to all low frequency barotropic oceanic motions. Over much of the ocean, the response has both the character of a large-scale and a superposed Rossby wave-like character, thus vindicating two apparently conflicting earlier interpretations. To the extent that free waves are excited they are consistent with their being dominated by Rossby and topographic Rossby wave components, although gravity modes are also necessarily excited to some degree. In general, a modal representation is not very helpful. The most active regions are the Southern Ocean and the western and northern North Atlantic. These results are stable to changes in geometry, topography, and tide period. On a global average basis, the dynamical response of Mm is closer to equilibrium than is Mf.  相似文献   
30.
Framvaren, a super-anoxic fjord in southern Norway, contains 7–8 mmoll−1 of sulphide and a total carbonate concentration of 18.5 mmol kg−1 in the bottom water. The chemistry of calcium has been studied, considering sources, biogenic and chemical processes and sedimentary sinks. Calcium associated with the bacteria biomass at the redox interface (18m depth) appears to be the primary source of dissolved calcium in the deep, anoxic water. Excess calcium and high total carbonate cause supersaturation of calcite, which is precipitated chemogenically. Calcite (and presumably some aragonite) is identified both in sediment trap material and the bottom sediments below the depth of supersaturation.  相似文献   
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