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   5820篇
  免费   28篇
  国内免费   50篇
系统科学   80篇
丛书文集   114篇
教育与普及   250篇
理论与方法论   19篇
现状及发展   303篇
研究方法   691篇
综合类   4439篇
自然研究   2篇
  2022年   7篇
  2019年   10篇
  2014年   15篇
  2013年   14篇
  2012年   373篇
  2011年   433篇
  2010年   134篇
  2009年   100篇
  2008年   444篇
  2007年   499篇
  2006年   506篇
  2005年   585篇
  2004年   390篇
  2003年   373篇
  2002年   336篇
  2001年   286篇
  2000年   442篇
  1999年   127篇
  1998年   47篇
  1997年   25篇
  1996年   22篇
  1995年   10篇
  1994年   23篇
  1993年   23篇
  1992年   15篇
  1991年   24篇
  1990年   31篇
  1989年   28篇
  1988年   20篇
  1987年   20篇
  1986年   28篇
  1985年   26篇
  1984年   27篇
  1983年   24篇
  1982年   26篇
  1981年   35篇
  1980年   8篇
  1979年   13篇
  1978年   9篇
  1977年   7篇
  1971年   12篇
  1970年   27篇
  1966年   9篇
  1959年   39篇
  1958年   53篇
  1957年   43篇
  1956年   28篇
  1955年   33篇
  1954年   31篇
  1948年   15篇
排序方式: 共有5898条查询结果,搜索用时 31 毫秒
61.
本书是结合分析力学和系统动力学发展起来的一种新的多学科动力学系统建模方法。这种新的建模技术基于拉格朗日能量法,依次生成一系列适合数值积分的微分代数方程。本书适用的建模方法是能建模和仿真的六连杆闭链机构或晶体管功率放大器等系统。  相似文献   
62.
方向包围盒(Oriented bounding box:OBB)的构造以及包围盒的相交测试的计算量都比较大,严重影响了在模拟、仿真的应用,尤其是有变形物体的场景。引入近似凸包的思想提出一种快速构造方向包围盒算法,很大程度上减少了构造方向包围盒(0BB)层次结构的顶点数,改进后的算法在降低构造层次结构时间的同时,对方向包围盒的紧密性代价几乎没有影响,在有些时候还提高了包围盒的紧密性。在包围盒相交测试方面,提留了一种基于筒单羽以爱的相交须刿方击,该算法在检测过程中省去了大量包围盒的相交测试计算,提高了相交测试的速度。最后将两种改进算法联合的碰撞检测框架与常用的基于均值和协方差矩阵的包围盒构造和基于分裂轴的算法进行比较,证明了算法具有高效性。  相似文献   
63.
Butler D 《Nature》2007,447(7140):6-7
  相似文献   
64.
65.
A fundamental question in nuclear physics is what combinations of neutrons and protons can make up a nucleus. Many hundreds of exotic neutron-rich isotopes have never been observed; the limit of how many neutrons a given number of protons can bind is unknown for all but the lightest elements, owing to the delicate interplay between single particle and collective quantum effects in the nucleus. This limit, known as the neutron drip line, provides a benchmark for models of the atomic nucleus. Here we report a significant advance in the determination of this limit: the discovery of two new neutron-rich isotopes--40Mg and 42Al--that are predicted to be drip-line nuclei. In the past, several attempts to observe 40Mg were unsuccessful; moreover, the observation of 42Al provides an experimental indication that the neutron drip line may be located further towards heavier isotopes in this mass region than is currently believed. In stable nuclei, attractive pairing forces enhance the stability of isotopes with even numbers of protons and neutrons. In contrast, the present work shows that nuclei at the drip line gain stability from an unpaired proton, which narrows the shell gaps and provides the opportunity to bind many more neutrons.  相似文献   
66.
The ability of mass spectrometry to generate intact biomolecular ions efficiently in the gas phase has led to its widespread application in metabolomics, proteomics, biological imaging, biomarker discovery and clinical assays (namely neonatal screens). Matrix-assisted laser desorption/ionization (MALDI) and electrospray ionization have been at the forefront of these developments. However, matrix application complicates the use of MALDI for cellular, tissue, biofluid and microarray analysis and can limit the spatial resolution because of the matrix crystal size (typically more than 10 mum), sensitivity and detection of small compounds (less than 500 Da). Secondary-ion mass spectrometry has extremely high lateral resolution (100 nm) and has found biological applications although the energetic desorption/ionization is a limitation owing to molecular fragmentation. Here we introduce nanostructure-initiator mass spectrometry (NIMS), a tool for spatially defined mass analysis. NIMS uses 'initiator' molecules trapped in nanostructured surfaces or 'clathrates' to release and ionize intact molecules adsorbed on the surface. This surface responds to both ion and laser irradiation. The lateral resolution (ion-NIMS about 150 nm), sensitivity, matrix-free and reduced fragmentation of NIMS allows direct characterization of peptide microarrays, direct mass analysis of single cells, tissue imaging, and direct characterization of blood and urine.  相似文献   
67.
Henzler-Wildman K  Kern D 《Nature》2007,450(7172):964-972
Because proteins are central to cellular function, researchers have sought to uncover the secrets of how these complex macromolecules execute such a fascinating variety of functions. Although static structures are known for many proteins, the functions of proteins are governed ultimately by their dynamic character (or 'personality'). The dream is to 'watch' proteins in action in real time at atomic resolution. This requires addition of a fourth dimension, time, to structural biology so that the positions in space and time of all atoms in a protein can be described in detail.  相似文献   
68.
South-polar features on Venus similar to those near the north pole   总被引:1,自引:0,他引:1  
Venus has no seasons, slow rotation and a very massive atmosphere, which is mainly carbon dioxide with clouds primarily of sulphuric acid droplets. Infrared observations by previous missions to Venus revealed a bright 'dipole' feature surrounded by a cold 'collar' at its north pole. The polar dipole is a 'double-eye' feature at the centre of a vast vortex that rotates around the pole, and is possibly associated with rapid downwelling. The polar cold collar is a wide, shallow river of cold air that circulates around the polar vortex. One outstanding question has been whether the global circulation was symmetric, such that a dipole feature existed at the south pole. Here we report observations of Venus' south-polar region, where we have seen clouds with morphology much like those around the north pole, but rotating somewhat faster than the northern dipole. The vortex may extend down to the lower cloud layers that lie at about 50 km height and perhaps deeper. The spectroscopic properties of the clouds around the south pole are compatible with a sulphuric acid composition.  相似文献   
69.
Butler D 《Nature》2007,449(7163):644-645
  相似文献   
70.
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