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1.
Macrophyte community diversity and composition respond to ecosystem conservation and local environmental factors. In this study, we developed a multidimensional diversity framework for macrophyte communities, including the taxonomic and functional alpha and beta diversity. We used the framework to explore the relationships among water level regimes and these diversity parameters in a case study of China's Baiyangdian Lake. Analysis of indicators of hydrologic alteration divided the water level from 1959 to 2019 into four regimes (dry, <6.42 m; low, 6.42–7.23 m; medium, 7.23–8.19 m; high, >8.19 m). Alpha and beta diversity were significantly higher in the medium regime than in the low and high regimes. Redundancy analysis indicated that the maximum water depth significantly affected taxonomic alpha diversity, and total nitrogen (TN) and chemical oxygen demand (COD) concentration significantly affected functional alpha diversity, respectively. Mantel tests showed that TN, Secchi depth (SD), and water depth in the high water level regime significantly increased the total beta diversity and turnover components. TN was the main factor that increased total taxonomic beta diversity. Water level regime mainly influenced interspecific relationships by changing the TN and COD concentration. The water level should be maintained between the medium and high water level regimes to promote restoration of the macrophyte community and improve ecosystem stability. The biodiversity evaluation framework would provide a deeper insight into the hydrological process management for restoration of aquatic macrophyte communities in shallow lakes. 相似文献
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M.P. Collings J.W. Dever H.J. Fraser M.R.S. McCoustra 《Astrophysics and Space Science》2003,285(3-4):633-659
The interaction of carbon monoxide (CO) with vapour-deposited water(H2O) ices has been studied using temperature programmed desorption (TPD) and Fourier transform reflection-absorption infrared
spectroscopy (FT-RAIRS) over a range of astrophysically relevant temperatures. Such measurements have shown that CO desorption
from amorphous H2Oices is a much more complex process than current astrochemical models suggest. Re-visiting previously reported laboratory
experiments (Collings et al., 2003), a rate model has been constructed to explain, in a phenomenological manner, the desorption
of CO over astronomically relevant time scales. The model presented here can be widely applied to a range of astronomical
environments where depletion of CO from the gas phase is relevant. The model accounts for the two competing processes of CO
desorption and migration, and also enables the entrapment of some of the CO in the ice matrix and its subsequent release as
the water ice crystallises and then desorbs. The astronomical implications of this model are discussed.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
4.
本文使用红外天文卫星(IRAS)巡天数据的最新版本IRAS天空巡天图(ISSA),经过进一步处理,得到了S140S141和S142SharplessHII区-分子云复合体的红外发射强度、温度及其光深的分布.在此基础上对各HII区的一些物理参量进行了统计分析,得到了分子云复合体的红外发射总光度以及复合体中尘埃的分布情况,对小尺度尘埃(VSG)的丰度进行了分析.并对各恒星形成区中的致密团块进行了研究,揭示出其中一些可能的恒星形成区域.同时,对S140区中的有关红外点源作出了能谱分析,并对S141区的激发星进行了讨论. 相似文献
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R. Papoular 《Monthly notices of the Royal Astronomical Society》2005,362(2):489-497
A model is proposed for the formation of water ice mantles on grains in interstellar clouds. This occurs by direct accretion of monomers from the gas, be they formed by gas or surface reactions. The formation of the first monolayer requires a minimum extinction of interstellar radiation, sufficient to lower the grain temperature to the point where thermal evaporation of monomers is just offset by monomer accretion from the gas. This threshold is mainly determined by the adsorption energy of water molecules on the grain material; for hydrocarbon material, chemical simulation places this energy between 0.5 and 2 kcal mol−1 , which sets the (true) visible extinction threshold at a few magnitudes. However, realistic distributions of matter in a cloud will usually add to this an unrelated amount of cloud core extinction, which can explain the large dispersion of observed (apparent) thresholds. Once the threshold is crossed, all available water molecules in the gas are quickly adsorbed, because the grain cools down and the adsorption energy on ice is higher than on bare grain. The relative thickness of the mantle, and, hence, the slope of τ3 ( A v ) depend only on the available water vapour, which is a small fraction of the oxygen abundance. Chemical simulation was also used to determine the adsorption sites and energies of O and OH on hydrocarbons and study the dynamics of formation of water molecules by surface reactions with gaseous H atoms, as well as their chances to stick in situ. 相似文献
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《中国地理科学(英文版)》2004,14(4):296-303
1INTRODUCTIONUrbanrelationshipaswellasurbansystemhas beenthemostimportantandlastingdirectioninthestudyofur-bangeographysinceCHRISTALLER(1933)putfor-wardthecentralplacetheory.Alongwiththepaceofglobalizationinthe1980s,somepioneer researchessen-sitivelyexpoundedaworldcitysystem,includingworldcity,internationalcity,nationalcity,regionalcityandlocalcity(FRIEDMAN,1986).Lotsofresearchesfo-cusedonthedevelopingmechanismofthebigcitiesandurbansystemnetwork(GU,2000;ZHOU,1997;CUI,1992;HUeta… 相似文献
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This paper reports results from an experiment designed to measure the nascent rovibrational population of H2 molecules that have formed through the heterogeneous recombination of H atoms on the surface of cosmic dust analogues under
conditions approaching those of the interstellar medium (ISM). H2 that has formed on a highly oriented pyrolytic graphite (HOPG) surface has been detected, using laser induced resonance-enhanced
multi-photon ionization (REMPI), in the v = 1 (J= 0–3) rovibrational states at surface temperatures of 30 K and 50 K. These excited product molecules display rotational temperatures
significantly higher than the target surface temperature. These first results suggest that a considerable proportion of the
binding energy released on formation of the H2 is deposited in the surface, in addition to internal excitation of the product molecules.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
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