首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   291095篇
  免费   1885篇
  国内免费   1001篇
化学   141095篇
晶体学   4016篇
力学   14963篇
综合类   6篇
数学   54534篇
物理学   79367篇
  2020年   1972篇
  2019年   2265篇
  2018年   13391篇
  2017年   13158篇
  2016年   10189篇
  2015年   3187篇
  2014年   4091篇
  2013年   9537篇
  2012年   10535篇
  2011年   18610篇
  2010年   11534篇
  2009年   11790篇
  2008年   14501篇
  2007年   16666篇
  2006年   7811篇
  2005年   8165篇
  2004年   7626篇
  2003年   7541篇
  2002年   6471篇
  2001年   6167篇
  2000年   4953篇
  1999年   3600篇
  1998年   3179篇
  1997年   3171篇
  1996年   3010篇
  1995年   2437篇
  1994年   2500篇
  1993年   2544篇
  1992年   2650篇
  1991年   2722篇
  1990年   2610篇
  1989年   2591篇
  1988年   2519篇
  1987年   2492篇
  1986年   2416篇
  1985年   3084篇
  1984年   3239篇
  1983年   2597篇
  1982年   2867篇
  1981年   2742篇
  1980年   2547篇
  1979年   2761篇
  1978年   2868篇
  1977年   2874篇
  1976年   2848篇
  1975年   2704篇
  1974年   2676篇
  1973年   2839篇
  1972年   1892篇
  1967年   1846篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
131.
In the present work, a quantitative analysis of the phase compositions by Mössbauer effect spectroscopy of solid and conventional hydrogen disproportionated Pr13.7Fe80.3B6.0 and Pr13.7Fe63.5Co16.7Zr0.1B6.0 alloys was carried out. Significant amounts of intermediate borides t-Fe3B and Pr(Fe, Co)12B6 were detected after solid hydrogen disproportionation treatment in Pr13.7Fe80.3B6.0 and Pr13.7Fe63.5Co16.7Zr0.1B6.0 alloys, respectively. After conventional hydrogenation–disproportionation–desorption–recombination treatment these phases were not detected and in no case residual Pr2Fe14B-phase was found. It was observed that the amount of intermediate borides after disproportionation can be correlated with the degree of texture after recombination at various temperatures.  相似文献   
132.
Based on the analysis of the K2O-P2O5-D2O solubility phase diagram, the optimum conditions of KD2PO4 crystallization—the compositions of mother solutions and the temperature range of crystallization—in the KH2PO4-D2O system have been determined. The technique of K(DxH1 ? x )2PO4 growth is developed. The DKDP single crystals with deuterium concentration up to 88 wt % are grown on DKDP seeds from KH2PO4 solutions in D2O by the method of temperature decrease.  相似文献   
133.
Translated from Chislennye Metody Resheniya Obratnykh Zadach Matematicheskoi Fiziki, pp. 147–153.  相似文献   
134.
135.
The interaction of water-soluble cationic 5,10,15,20-tetrakis(4-N-methyl pyridyl) porphyrin (H2TMPyP4) with some mono-and polynucleotides is studied by time-resolved and steady-state fluorescence spectroscopy, as well as by steady-state absorption spectroscopy. The fluorescence decay kinetics are analyzed by reconstructing the decay time distributions, which made it possible to describe in more detail than previously the complexes formed due to the interaction. The main effect of binding of H2TMPyP4 adenosine 5′-monophosphate and to poly(dA-dT)2 is shown to be an increase in the fluorescence lifetime from 4.6 ns in the solution to 8.3 and 12.3 ns, respectively. This effect is explained by a less polar (in comparison with water) environment of porphyrin in complexes, which leads to a decrease in the quenching action of the intramolecular charge transfer state between the porphyrin macrocycle and methyl pyridyl groups. In the case of complex formation with guanine-containing nucleotides (guanosine 5′-monophosphate and poly(dG-dC)2), the effect of decrease in the quenching action of the intramolecular charge transfer state caused by a decrease in the medium polarity is superimposed by a stronger effect of decrease in the fluorescence lifetime of porphyrin as a result of intermolecular electron transfer from guanine to excited porphyrin. A high sensitivity of this intermolecular quenching to the mutual arrangement of the electron donor and the electron acceptor makes it possible to reveal four types of complexes between H2TMPyP4 and guanosine 5′-monophosphate, which differ in the positions of four broad peaks in the porphyrin fluorescence decay time distribution (0.1, 0.7, 2.4, and 6.1 ns). For the complex with poly(dG-dC)2, a narrow peak at 2.8 ns prevails in the fluorescence decay time distribution, with the contributions from two additional narrow peaks at 1.0 and 6.2 ns being small.  相似文献   
136.
137.
ABSTRACT. Limiting adverse consequences of fishing on essential fish habitat has emerged as a key fishery management objective. The conventional approach to providing habitat protection is to create MPAs or marine reserves that prohibit all or certain types of fishing in specific areas. However, there may be more cost‐effective and flexible ways to provide habitat protection. We propose an individual habitat quota (IHQ) system for habitat conservation that would utilize economic incentives to achieve habitat conservation goals cost‐effectively. Individual quotas of habitat impact units (HIU) would be distributed to fishers with an aggregate quota set to maintain a target habitat “stock.” HIU use would be based on a proxy for marginal habitat damage. We use a dynamic, explicitly spatial fishery and habitat simulation model to explore how such a system might work. We examine how outcomes are affected by spatial heterogeneity in the fishery and the scale of habitat regulation. We find that the IHQ system is a highly cost‐effective means of ensuring a given level of habitat protection, but that spatial heterogeneity and the scale of regulation can have significant effects on the distribution of habitat protection.  相似文献   
138.
139.
140.
Approximate properties of variable measures compose a base of the two-scale convergence method with respect to a variable measure, which is used in averaging on periodic thin and composite structures. The paper gives a survey of methods for verifying approximate properties. The main focus is on studying composite measures, which have been little studied. __________ Translated from Sovremennaya Matematika i Ee Prilozheniya (Contemporary Mathematics and Its Applications), Vol. 16, Partial Differential Equations, 2004.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号