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61.
Utah prairie dogs were transplanted onto the site of a former colony, located in Capitol Reef National Park, Utah. Shrubs on the site were significantly taller than those found on active colonies in similar habitat located on the Awapa Plateau. Therefore, the transplant site afforded a test of the hypothesis that shrub height is a major inhibitory factor affecting occupation of sites by prairie dogs. Four sites of 5 ha each were used. Vegetation treatments — rotobeating, railing, and 2,4 - D herbicide — were carried out on three of the sites and the fourth was used as a control. Shrub height and percent cover were significantly reduced on all three treatment sites. Posttreatment effects on the vegetation showed that the greatest percent moisture of the herbage was found on the railed site, followed by the herbicide, rotobeaten, and control sites. Measurements of the visual obstructions to prairie dogs showed that the rotobeaten site had the greatest visibility, followed by the railed, herbicide, and control sites. Prior to release of prairie dogs on the study area, 200 artificial burrows per treatment were dug, using a power auger. In early summer, 1979, 200 Utah prairie dogs were live - trapped near Loa, Utah. An equal number by sex and age class were released on each treatment. In 1979 a significantly higher number of animals reestablished on the rotobeaten site. In 1980 and 1981 the rotobeaten and railed sites had significantly higher prairie dog numbers than the other sites. Reproduction occurred on both the rotobeaten and railed sites in 1980 and 1981. Results indicated that, when transplanting animals onto sites of former colonies presently overgrown with shrubs, the chances of a successful transplant could be increased by first reducing shrub height and density. 相似文献
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This paper proposes a new mixture GARCH model with a dynamic mixture proportion. The mixture Gaussian distribution of the error can vary from time to time. The Bayesian Information Criterion and the EM algorithm are used to estimate the number of parameters as well as the model parameters and their standard errors. The new model is applied to the S&P500 Index and Hang Seng Index and compared with GARCH models with Gaussian error and Student's t error. The result shows that the IGARCH effect in these index returns could be the result of the mixture of one stationary volatility component with another non‐stationary volatility component. The VaR based on the new model performs better than traditional GARCH‐based VaRs, especially in unstable stock markets. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
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又发现了两种新水。要是没有水,我们原本不会来到这个世界。水的热容量在-45℃时应该变成无穷大。水的其它特性似乎也变得一团糟,就像水经历了某种灾变一样,为什么?如果想象在太平洋之下11公里处的马里亚那海沟中即在海洋最深之处的高压之下,人还能生活,便会看到这是一个寂静的、永远黑暗的世界,压力高达1000个大气压。那是一座相当于洋底每平方米承受1000吨压力的海水之增。在如此恶劣的条件下,生存必定不易。然而现在有些物理学家相信在这样高的压力下甚至水本身可能也难于保持不变。他们认为如果在以上压力下水若能保持不变即仍… 相似文献
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Philip Bromiley 《Journal of forecasting》1987,6(3):201-210
In attempting to improve forecasting, many facets of the forecasting process may be addressed including techniques, psychological factors, and organizational factors. This research examines whether a robust psychological bias (anchoring and adjustment) can be observed in a set of organizationally-produced forecasts. Rather than a simple consistent bias, biases were found to vary across organizations and items being forecast. Such bias patterns suggest that organizational factors may be important in determining the biases found in organizationally-produced forecasts. 相似文献
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A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 总被引:18,自引:0,他引:18
Loeys BL Chen J Neptune ER Judge DP Podowski M Holm T Meyers J Leitch CC Katsanis N Sharifi N Xu FL Myers LA Spevak PJ Cameron DE De Backer J Hellemans J Chen Y Davis EC Webb CL Kress W Coucke P Rifkin DB De Paepe AM Dietz HC 《Nature genetics》2005,37(3):275-281
We report heterozygous mutations in the genes encoding either type I or type II transforming growth factor beta receptor in ten families with a newly described human phenotype that includes widespread perturbations in cardiovascular, craniofacial, neurocognitive and skeletal development. Despite evidence that receptors derived from selected mutated alleles cannot support TGFbeta signal propagation, cells derived from individuals heterozygous with respect to these mutations did not show altered kinetics of the acute phase response to administered ligand. Furthermore, tissues derived from affected individuals showed increased expression of both collagen and connective tissue growth factor, as well as nuclear enrichment of phosphorylated Smad2, indicative of increased TGFbeta signaling. These data definitively implicate perturbation of TGFbeta signaling in many common human phenotypes, including craniosynostosis, cleft palate, arterial aneurysms, congenital heart disease and mental retardation, and suggest that comprehensive mechanistic insight will require consideration of both primary and compensatory events. 相似文献
70.
Jadeja S Smyth I Pitera JE Taylor MS van Haelst M Bentley E McGregor L Hopkins J Chalepakis G Philip N Perez Aytes A Watt FM Darling SM Jackson I Woolf AS Scambler PJ 《Nature genetics》2005,37(5):520-525
Fraser syndrome is a recessive, multisystem disorder presenting with cryptophthalmos, syndactyly and renal defects and associated with loss-of-function mutations of the extracellular matrix protein FRAS1. Fras1 mutant mice have a blebbed phenotype characterized by intrauterine epithelial fragility generating serous and, later, hemorrhagic blisters. The myelencephalic blebs (my) strain has a similar phenotype. We mapped my to Frem2, a gene related to Fras1 and Frem1, and showed that a Frem2 gene-trap mutation was allelic to my. Expression of Frem2 in adult kidneys correlated with cyst formation in my homozygotes, indicating that the gene is required for maintaining the differentiated state of renal epithelia. Two individuals with Fraser syndrome were homozygous with respect to the same missense mutation of FREM2, confirming genetic heterogeneity. This is the only missense mutation reported in any blebbing mutant or individual with Fraser syndrome, suggesting that calcium binding in the CALXbeta-cadherin motif is important for normal functioning of FREM2. 相似文献