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961.
A thick sequence of mafic-ultramafic rocks, occurs along a major shear zone (Phulad lineament), running across the length of Aravalli Mountain Range for about 300 kms. It has been suggested, that this sequence may represent a fragment of ophiolite or a rift related metavolcanic suite made up of basalts and fractionated ultramafics. The geological and tectonic significance of the complex is assessed using field relationships, petrography and geochemistry. Structurally, the lowest part of the complex comprises a discontinuous band of plastically deformed harzburgite (mantle component) followed by layered cumulus gabbroic rocks (crustal component). A complex of non-cumulus rocks comprising hornblende schists, gabbros, sheeted dykes and pillowed basalts structurally overlies layered gabbros. Huge bodies of diorite intrude volcanics.

Geochemical classification suggests that all non-cumulus mafic rocks are sub-alkaline basalts except one variety of dykes which shows mildly alkaline character. The sub-alkaline rocks are tholeiite to calc-alkaline with boninite affinity. Tectono-magmatic variation diagrams and MORB normalised patterns suggest a fore arc tectonic regime for the eruption of these rocks.

The mafic rocks of Phulad Ophiolite Suite are zoned across the strike in terms of their distribution from west to east. The hornblende schists and basalts are exposed at the westernmost margin followed by gabbros and dykes. The alkaline dyke occurs at the easternmost part. The rocks of Phulad suite are juxtaposed with shallow water sediments in the east followed by platformal sediments and then continental slope sediments in the further east indicating gradual thickening of the crust from west to east and an eastward subduction. The geochemical interpretation presented in this study, together with discussion of lithological association is used to decipher the tectonic evolution of the Mesoproterozoics of NW Indian shield.  相似文献   

962.
The objective of this work is to assess the concentrations of three factions of air particles (settable particles, TSP and PM10) and the levels of several toxic elements in a clay atomisation industry through aerosol sampling at several points inside an industrial plant. Mechanical activities, which produce diffuse emissions, are the main process of discharge of particles in both indoor and outdoor workplace environments in the atomisation plant. The levels of As, Cd, Pb, Zn, Ba and Ni increase in the zones with higher concentrations of particles and lower ventilation. The concentrations of As and F are not influenced by the recycling processes. The levels of Cd and Pb do not show great enrichment in air particles collected inside the atomisation plant although the content of both elements is associated with ceramic muck recycling. Finally, the content of B in waste water is mainly transferred in gaseous phase to the atmosphere during the process of drying by atomisation.  相似文献   
963.
964.
A series of geotechnical centrifuge physical modeling tests were performed to assess the potential use of a new cost-effective mechanically stabilized earth system for retrofitting marginally stable cohesive slopes. The proposed system utilizes the dual functions of reinforcement and drainage by directly inserting high strength non-woven geotextile strips into slopes, with little or no excavation required behind the slope face. The system significantly increases the factor of safety of potentially unstable cohesive slopes, and can be constructed at less expense and more rapidly than conventional mechanically stabilized earth systems.  相似文献   
965.
966.
Summary Oxygen isotope ratios of igneous zircon from magmatic rocks in Finland provide insights into the evolution and growth of the Precambrian crust during the Svecofennian orogeny. These data preserve magmatic δ18O values and correlate with major discontinuities in the lower crust. Oxygen isotope ratios of zircon across the 1.88–1.87 Ga Central Finland granitoid complex (CFGC) range from 5.50‰ to 6.84‰, except for three plutons in contact with the adjacent greenstone and metasedimentary belts (δ18O(Zrc) = 7.60‰–7.78‰). There is a systematic variation in δ18O(Zrc) with respect to geographic location in the CFGC, ranging from 6.60±0.23‰ (σ) in the northeast to 5.90±0.40‰ in the west-southwest. These values correlate with a change in crustal thickness and shift in geochemical composition. The oxygen isotope composition of the 1.65–1.54 Ga rapakivi granites and related rocks in southern Finland show a decreasing trend from north to south, independent of their emplacement age. The southern anorogenic granite group has an average δ18O in zircon of 6.14±0.07‰ and the northern anorogenic group has an average δ18O in zircon of 8.14±0.59‰. This difference reflects the boundary between island arc terrains accreted during the Paleoproterozoic. Deceased  相似文献   
967.
968.
Marine transgression onto the South American continent took place at least twice in the Miocene along distinct paleogeographic corridors. The first event occurred between 15 and 13 Ma and the second between 10 and 5? Ma. Each event has particular dominant variables (tectonism, eustacy, sediment accumulation rate) that permitted the preservation of the record and development of the sea on the continent. The 15–13 Ma transgression was tectonically and eustatically controlled, flooding older sedimentary accommodation zones on the South American plate during a global high sea level, whereas the 105? Ma event was predominantly tectonically controlled, generated by tectonic loading created in the Cordillera Oriental fold-and-thrust belt. A new 7.72±0.31 Ma 40Ar/39Ar date from the Río Parapetí in Bolivia suggests that the 15–13 Ma transgression registered in Argentina produced no continental connection to the Caribbean transgression, registered in Bolivia, because of temporal constraints.  相似文献   
969.
Development of chemical industry and high vapor pressure of volatile organic compounds (VOCs) have been caused that these materials recently be considered as a source of air pollution. These are different methods for separation of VOC from air that absorption by suitable and selective solvent is an efficient method. In this research, mathematical modeling of a packed absorption tower for separation of VOCs from air has been presented. Then, acetone vapors separation in this tower and with Intalox saddle packing has been investigated. Concentration of acetone in inlet air stream was 1.5 mol % which has reduced to 150 ppm (0.015 mol %) in effluent air stream. The results show that the packed absorption tower with this type of packing can separate 99% of acetone vapors. Comparison of the results obtained by Intalox saddle packing with the results obtained by another type of packing (with trade mark of Kerapak patented by Sulzer Company) shows that the tower gives the same efficiency for acetone separation. Thus, the efficiency of absorption process, mainly, depends on solvent type, composition of VOC in feed air, desired composition of VOC in outlet air (or percentage of VOC separation) and pressure drop.  相似文献   
970.
Many Recent and fossil freshwater tufa stromatolites contain millimetre‐scale, alternating laminae of dense micrite and more porous or sparry crystalline calcites. These alternating laminae have been interpreted to represent seasonally controlled differences in the biotic activity of microbes, and/or seasonally controlled changes in the rate of calcification. Either way, couplets of these microbially mediated alternating calcified laminae are generally agreed to represent annual seasonality. Combined stable isotope (δ18O and δ13C) and trace element (Mg, Sr, Ba) geochemistry from Recent tufa stromatolites show that seasonal climatic information is available from these calcites. Variability in δ18O (and in one case Mg concentration) has been shown to be controlled primarily by stream temperature change, usually driven by solar insolation. In arid climates, seasonal evaporation can also cause δ18O enrichment by at least 1‰. Variability in δ13C results potentially from: (1) seasonal change in plant uptake of 12C‐enriched CO2; (2) seasonal change in degassing of 12C‐enriched CO2 in the aquifer system; and (3) precipitation of calcite along the aquifer or river flow path, a process that increases δ13C of dissolved inorganic carbon (DIC) in the remaining water. Mechanisms 2 and 3 are linked because calcite precipitates in aquifers where degassing occurs, e.g. air pockets. The latter mechanism for δ13C enrichment has also been shown to cause sympathetic variation between trace element/Ca ratios and δ13C because trace elements with partition coefficients much greater than 1 (e.g. Sr, Ba) remain preferentially in solution. Since degassing in air pockets will be enhanced during decreased recharge when water saturation of the aquifer is lowest, sympathetic variation in trace element/Ca ratios and δ13C is a possible index of recharge and therefore precipitation intensity. High‐resolution geochemical data from well‐dated tufa stromatolites have great potential for Quaternary palaeoclimate reconstructions, possibly allowing recovery of annual seasonal climatic information including water temperature variation and change in rainfall intensity. However, careful consideration of diagenetic effects, particularly aggrading neomorphism, needs to be the next step. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   
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