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131.
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We investigate the phylogeny, biogeography, time of origin and diversification, ancestral area reconstruction and large‐scale distributional patterns of an ancient group of arachnids, the harvestman suborder Cyphophthalmi. Analysis of molecular and morphological data allow us to propose a new classification system for the group; Pettalidae constitutes the infraorder Scopulophthalmi new clade , sister group to all other families, which are divided into the infraorders Sternophthalmi new clade and Boreophthalmi new clade . Sternophthalmi includes the families Troglosironidae, Ogoveidae, and Neogoveidae; Boreophthalmi includes Stylocellidae and Sironidae, the latter family of questionable monophyly. The internal resolution of each family is discussed and traced back to its geological time origin, as well as to its original landmass, using methods for estimating divergence times and ancestral area reconstruction. The origin of Cyphophthalmi can be traced back to the Carboniferous, whereas the diversification time of most families ranges between the Carboniferous and the Jurassic, with the exception of Troglosironidae, whose current diversity originates in the Cretaceous/Tertiary. Ancestral area reconstruction is ambiguous in most cases. Sternophthalmi is traced back to an ancestral land mass that contained New Caledonia and West Africa in the Permian, whereas the ancestral landmass for Neogoveidae included the south‐eastern USA and West Africa, dating back to the Triassic. For Pettalidae, most results include South Africa, or a combination of South Africa with the Australian plate of New Zealand or Sri Lanka, as the most likely ancestral landmass, back in the Jurassic. Stylocellidae is reconstructed to the Thai‐Malay Penisula during the Jurassic. Combination of the molecular and morphological data results in a hypothesis for all the cyphophthalmid genera, although the limited data available for some taxa represented only in the morphological partition negatively affects the phylogenetic reconstruction by decreasing nodal support in most clades. However, it resolves the position of many monotypic genera not available for molecular analysis, such as Iberosiro, Odontosiro, Speleosiro, Managotria or Marwe, although it does not place Shearogovea or Ankaratra within any existing family. The biogeographical data show a strong correlation between relatedness and formerly adjacent landmasses, and oceanic dispersal does not need to be postulated to explain disjunct distributions, especially when considering the time of divergence. The data also allow testing of the hypotheses of the supposed total submersion of New Zealand and New Caledonia, clearly falsifying submersion of the former, although the data cannot reject the latter. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, 105 , 92–130.  相似文献   
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SUMMARY 1. The effects of chlorine on litter ( Potamogeton crispus L.) processing were examined using six outdoor experimental streams. Downstream portions of two streams were dosed at c . 10 μg l−1 Total Residual Chlorine (TRC), one stream at 64 μgl1, and one stream at 230μg l−1. Two control streams were not dosed; upstream riffles of each stream served as instream controls.
2. Two 35 day litter breakdown (per cent AFDW remaining) experiments indicated significantly lower decay rates in the high dose riffle. No other concentration of chlorine significantly affected decay rate.
3. A third experiment, conducted in medium and high dose streams, indicated that high dose chlorine exposure reduced litter decomposition rates significantly, and reduced microbial colonization, microbial electron transport system activity, and microbial litter decomposition after 4 days but not after 11 days of exposure. The number of amphipod shredders colonizing litter bags was also reduced significantly with high chlorine dose.
4. A fourth experiment, after dosing was terminated, provided direct evidence that amphipod shredders were important in facilitating litter decomposition: litter bags stocked with amphipods had significantly higher decomposition rates than bags which excluded shredders.
5. Overall results indicate that the high dose (c. 230 μgl−1 TRC) of chlorine reduced litter processing rates partly by reducing initial microbial conditioning, but primarily by reducing the colonization of amphipod shredders.  相似文献   
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Thigmonastic movements in the sensitive plant Mimosa pudica L., associated with fast responses to environmental stimuli, appear to be regulated through electrical and chemical signal transductions. The thigmonastic responses of M. pudica can be considered in three stages: stimulus perception, electrical signal transmission and induction of mechanical, hydrodynamical and biochemical responses. We investigated the mechanical movements of the pinnae and petioles in M. pudica induced by the electrical stimulation of a pulvinus, petiole, secondary pulvinus or pinna by a low electrical voltage and charge. The threshold value was 1.3–1.5 V of applied voltage and 2 to 10 µC of charge for the closing of the pinnules. Both voltage and electrical charge are responsible for the electro‐stimulated closing of a leaf. The mechanism behind closing the leaf in M. pudica is discussed. The hydroelastic curvature mechanism closely describes the kinetics of M. pudica leaf movements.  相似文献   
137.
The nonlinear mixed effects model with a smooth random effects density   总被引:6,自引:0,他引:6  
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138.
139.
We analyze territorial behavior in terms of decisions abouttime allocation.Such decisions must be made whenever time investedin territorial defense cannot be devoted to feeding, and viceversa. We describe the ecology and territorial behavior of thegreat tit (Parus major) to show that a tradeoff exists, andthen outline a series of laboratory and field experiments inwhich the value of feeding or defense was experimentally manipulated.Territorialmale great tits began to invest more heavily in territorialvigilance after encountering intruders, but the increase invigilance depended on the rate at which they could feed, aswell as their hunger level. We outline a dynamic analysis thattakes account of the fact that the optimal tradeoff will changeas hunger is reduced. The results of an experimental test ofthis dynamic model are also presented. We briefly review othertechniques whereby territorial tradeoffs have been investigated.  相似文献   
140.
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