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1.
Raphael Chalmeau 《Primates; journal of primatology》1994,35(3):385-392
The aim of this study was to assess the ability of chimpanzees (Pan troglodytes) to cooperate in an instrumental task. A specially constructed fruit distributor was presented to a group of six captive
chimpanzees. A cooperative response required two chimpanzees: both had to pull a handle simultaneously to make a fruit fall
into the cage. The dominant male of the group and an infant produced most of the operant responses, and the male got nearly
all the fruits. Other conspecifics avoided the dominant male at the apparatus. Social influences appear to limit the possibility
of co-operation between individuals because a certain level of interindividual tolerance is required. The results revealed
a significant increase in the number of pulls each time both chimpanzees were together at the apparatus. Operant chimpanzees
learn to coordinate their actions in time and space. 相似文献
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R. Shine F. Brischoux A. J. Pile 《Proceedings. Biological sciences / The Royal Society》2010,277(1693):2459-2464
Evolutionary transitions from terrestrial to aquatic life modify selective forces on an animal''s coloration. For example, light penetrates differently through water than air, and a new suite of predators and visual backgrounds changes the targets of selection. We suggest that an aquatic animal''s coloration may also affect its susceptibility to algal fouling. In a colour-polymorphic field population of seasnakes (Emydocephalus annulatus) in New Caledonia, black individuals supported higher algal cover than did banded conspecifics. In experimental tests, black snake models (plastic tubes) accumulated more algae than did banded models. Algal cover substantially reduced snake activity (in the field) and swimming speeds (in the laboratory). Effects of algal cover on a snake''s hydrodynamic efficiency and/or its rate of cutaneous gas exchange thus may impose selection on the colours of aquatic organisms. 相似文献
6.
Evolutionary constraint results from the interaction between the distribution of available genetic variation and the position of selective optima. The availability of genetic variance in multitrait systems, as described by the additive genetic variance-covariance matrix (G), has been the subject of recent attempts to assess the prevalence of genetic constraints. However, evolutionary constraints have not yet been considered from the perspective of the phenotypes available to multivariate selection, and whether genetic variance is present in all phenotypes potentially under selection. Determining the rank of the phenotypic variance-covariance matrix (P) to characterize the phenotypes available to selection, and contrasting it with the rank of G, may provide a general approach to determining the prevalence of genetic constraints. In a study of a laboratory population of Drosophila bunnanda from northern Australia we applied factor-analytic modeling to repeated measures of individual wing phenotypes to determine the dimensionality of the phenotypic space described by P. The phenotypic space spanned by the 10 wing traits had 10 statistically supported dimensions. In contrast, factor-analytic modeling of G estimated for the same 10 traits from a paternal half-sibling breeding design suggested G had fewer dimensions than traits. Statistical support was found for only five and two genetic dimensions, describing a total of 99% and 72% of genetic variance in wing morphology in females and males, respectively. The observed mismatch in dimensionality between P and G suggests that although selection might act to shift the intragenerational population mean toward any trait combination, evolution may be restricted to fewer dimensions. 相似文献
7.
The evolutionary mechanisms underlying the maintenance of invariant traits are poorly understood, partly because the lack of variance makes these mechanisms difficult to study. Although the number of cotyledons that plant species produce is highly canalized, populations of plants frequently contain individuals with abnormal cotyledon numbers. In a garden study with 1857 wild radish plants from 75 paternal half-sibling families, 89 (almost 5%) had cotyledon numbers less or greater than two. We found evidence for direct selection on cotyledon number, but no evidence for additive genetic variation for cotyledon number. In spite of the very large sample size, our power to detect variation and selection was hampered by the small number of individuals (10) producing more than two cotyledons. Thus, our results provide support for both a lack of genetic variation and selection as reasons for the current lack of variation in wild radish cotyledon number. 相似文献
8.
Cele Abad‐Zapatero 《Acta Crystallographica. Section D, Structural Biology》2009,65(12):1341-1349
Some of the current trends in the structure of evolutionary biology are reviewed using as a framework the book of the same title by S. J. Gould (1941–2002). The revised concepts and interpretations of the structure–function relationship in evolutionary biology are discussed in relation to the past achievements and future developments in structural biology. 相似文献
9.
Eric Jacquelin Denis Brizard Raphael Dumas 《Computer methods in biomechanics and biomedical engineering》2019,22(10):925-935
The study presents a screening method used to identify the influential parameters of a lower limb model including ligaments, at low numerical cost. Concerning multibody kinematics optimisation, the ligament parameters (isometric length) were found the most influential ones in a previous study. The screening method tested if they remain influential with minimised length variations. The most important parameters for tibiofemoral kinematics were the skin markers, segment lengths and joint parameters, including two ligaments. This was confirmed by a quantitative sensitivity analysis. The screening method has the potential to be used as a stand-alone procedure for a sensitivity analysis. 相似文献
10.
PAUL EGGLETON ROBERT BELSHAW 《Biological journal of the Linnean Society. Linnean Society of London》1993,48(3):213-226
We consider differences between dipteran, hymenopteran and coleopteran parasitoids in the following categories: taxonomic range and developmental stage of hosts attacked; habitats they are attacked in; developmental stage of the parasitoid contacting the host; occurrence of phoresy, and attacking hosts during flight. Using existing phylogenetic classifications we reconstruct possible ancestral conditions to the parasitoid clades in the three orders. By considering these as phylogenetic constraints and potentialities we attempt to account for the observed differences between the parasitoids within the orders. 相似文献