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321.
Recent research has highlighted the value of employing the idea of networks to describe the interrelatedness of today's globalizing economy. Networks facilitate flows of knowledge, ideas, managerial techniques and capital between firms both within and across political borders. This paper argues that the reconstruction of social connections through which information is created, given value and exchanged is fundamental to an understanding of not only contemporary but also historical patterns of economic globalization. We focus on the networks of the capitalist elite running 12 major multinational enterprises, active across British imperial territories, between c .1900 and c .1930. An examination is made of the economic and spatial interlocks between firms created by board members who were multiple directors. Social underpinnings of multiple directorates are examined by exploring the common, overlapping social spheres within which individuals engaged. A clearer grasp of the ways in which corporate activity operated in the early 1900s can provide a better understanding of the social context of global economic operations.  相似文献   
322.
Legal factors play an underrated but significant role as constraints on conservation management. In this paper, based on observations in both Northern Ireland and the Republic of Ireland, mode of land tenure is assessed to determine its influence on the conservation management of coastal dunes. The tenure types considered are: private ownership, corporate private ownership, tenancy, secured tenancy, leasing, common (joint) ownership, uncertain ownership, public ownership and its subset military ownership. It is suggested that multiple private ownership is least likely to favour effective conservation management. Public ownership by a statutory conservation authority and corporate private ownership by a conservation-orientated NGO are regarded as the optimum tenure types for conservation management of coastal dunes.  相似文献   
323.
A large landslide on the urban fringe of metropolitan Phoenix, Arizona   总被引:2,自引:1,他引:2  
A granitic rock avalanche, one of the largest Quaternary landslides in Arizona outside the Grand Canyon with a volume of approximately 5.25 M m3 and a width a little under 0.5 km, ran 1 km from the eastern McDowell Mountains. With lateral levees and pressure ridges, the rock avalanche deposit displays many features found on classic sturzstroms. Failure occurred along a major joint plane paralleling the slope with a dip of 44°, when a major base level lowering event in the Salt River system would have undermined the base of the failed slope, and probably during a period of more moisture than normally available in the present-day arid climate. Failure at the subsurface weathering front highlights the importance of the dramatic permeability change between grussified regolith and relatively fresh bedrock. Rock varnish microlaminations (VMLs) dating, in concert with other geomorphic evidence, suggests that the rock avalanche deposit is slightly older than 500 ka. The rock vanish results also have important implications for sampling strategies designed to use cosmogenic nuclide to date Quaternary landslide deposits. Discovery of a large landslide in close proximity to the extending urban fringe of metropolitan Phoenix argues for a more careful analysis of landslide hazards in the region, especially where rapid development excavates bedrock at the base of steep mountain slopes and where the subsurface weathering front is near the surface.  相似文献   
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Denitrification rates along a salinity gradient in the eutrophic Neuse River Estuary, North Carolina, were quantified using membrane inlet mass spectrometry (MIMS) within short-term batch incubations. Denitrification rates within the system were highly variable, ranging from 0 to 275 μmol N m−2 h−1. Intrasite variability increased with salinity, but no significant differences were observed across the salinity gradient. Denitrification rates were positively correlated with sediment oxygen demand at the upstream sampling site where sediment organic carbon levels were lowest. This relationship was not observed in the more saline sampling sites. Denitrification rates were highest during winter. On an annual basis, denitrification accounted for 26% of the dissolved inorganic nitrogen and 12% of the total nitrogen supplied to the system.  相似文献   
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327.
Graphical analysis of free-energy relationships involving binary quadruple points and their associated univariant equilibria in the system CO2-H2O suggests the presence of at least 2 previously unrecognized quadruple points and a degenerate binary invariant point involving an azeotrope between CO2-rich gas and liquid. Thermodynamic data extracted from the equilibrium involving clathrate (hydrate), gas, and ice (H = G+I) are employed along with published data to calculate the P-T range of the 3-ice equilibrium curve, S+I = H, where S is solid CO2. This equilibrium curve intersects the H = G+I curve approximately where the latter curve intersects the S+H = G curve, thus confirming the existence of one of the inferred quadruple points involving the phases S, G, H, and I. Recognition of some binary equilibria probably have been hampered by extremely low mutual solubilities of CO2 and H2O in the fluids phases which, for example, render the S+H = G virtually indistinguishable from the CO2-sublimation curve.To make the published portion of the L(liquid CO2)-G-H equilibrium “connect” with the other new quadruple point involving S, L, G, and H, it is necessary to change the sense of the equilibrium from L = G+H at higher pressures to L+H = G at lower pressures by positing a L = G azeotrope at very low concentrations of H2O. At the low-pressure origin of the azeotrope, which is only a few bars above the CO2-triple point, the azeotrope curve intersects the 3-phase curve tangentially, creating a degenerate invariant point at which the 3-phase equilibrium changes from L+H = G at lower pressures to L = G+H at higher pressures. The azeotrope curve is offset at slightly lower temperature from the L = G+H curve until the 3-phase equilibrium terminates at the quadruple point involving G, L, H, and W (water). With further increase in pressure the azeotrope curve tracks the L = G+W equilibrium and apparently terminates at a critical end point in close proximity to critical endpoints for the CO2-saturation curve and the L = G+W curve.Thermodynamic data for clathrate extracted from the slope of the H = G+I curve are consistent with a solid-state phase transformation in CO2-clathrate between 235 and 255 K. Published work shows that the type-I clathrate phase, whose atomic structure is a framework of water molecules with CO2 molecules situated in large “guest” sites within the framework, is variable in composition with ∼1 guest site vacancy per unit cell at the high-temperature limit of its stability; the number of water molecules, however, remains constant. The formula (CO2)8-y·46H2O, where y is the number of vacancies per unit cell, is in keeping with the atomic structure, whereas the traditional formula, CO2·nH2O, where n (hydration number) = 5.75, is misleading.Ambient P-T conditions in the Antarctic and Greenland ice sheets are compatible with sequestering large amounts of carbon as liquid CO2 and/or clathrate.  相似文献   
328.
Cesium-137 derived from the explosion of the Chernobyl reactor in 1986 was preserved in anoxic sediments from a coastal environment in southern Rhode Island. Although the radioactive plume was detected in surface air samples at several locations in the United States, this is the first known record of a Chernobyl 137Cs peak in sediments from North America. The inventory of Chernobyl 137Cs that was preserved in the Pettaquamscutt River is small compared to European counterparts and should only be detectable for the next 15-20 yr. However, the presence of two 137Cs peaks (1963 and 1987) identifies a well-dated segment of the sediment column that could be exploited in understanding the decomposition and preservation of terrestrial and aquatic organic matter. Different methods for calculating the 210Pb chronology were also evaluated in this study and checked against independent varve counting. The end result is a detailed chronology of a site well suited for reconstruction of historical records of environmental change.  相似文献   
329.
Ab initio quantum chemistry calculations have been performed on the isotopic exchange reaction between B(OH)3 and B(OH)4. Several calculation methods have been carefully compared and evaluated. The “water-droplet” method is chosen to investigate this isotope exchange reaction using cluster models with up to 34 water molecules surrounding the solute. HF/6-31G* level calculations coupled with a 0.920 scaling factor are used for the frequency calculations. A larger K value (1.027) is obtained from this study compared to the commonly used 1.0194 (Kakihana et al., 1977).The fractionations for several boric acid polymers and boron minerals are also studied. Our results suggest that assuming the BO4 bonding in B(OH)4 is identical to that in borosilicates is wrong. Tetrahedral boron in silicates has a significantly smaller reduced isotopic partition function ratio (RPFR) and hence will be much isotopically lighter than in B(OH)4.The new theoretical curve of pH vs. δ11B composition of B(OH)4 using our calculated 1.027 can be used to predict pH values for equilibrium cases such as incorporation into inorganic calcite. We also find that the shape of this curve is very sensitive to both K and pKa value, giving the possibility of also predicting salinity from the different shapes of the curve.  相似文献   
330.
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