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71.
1. Stable isotopes of nitrogen are useful for quantifying the trophic structure of food webs, but only if the variation in trophic enrichment (ΔN), which is the difference in δ15N between a consumer and its food, is small relative to the value of ΔN itself. 2. We examined the sources of variation in zooplankton ΔN by measuring the trophic enrichment (ΔN) of seven species of freshwater cladocerans, and by testing for an effect of age and temperature on the ΔN of Daphnia pulicaria. 3. We found that ΔN was similar among Cladocera and was not correlated with body size. Overall, the ΔN for D. pulicaria was 1.4‰ (SE = 0.69, n = 57), as was expected for the detritus diet that we used in our experiments. We found no effect of temperature (15–25 °C) on ΔN, but found that ΔN of D. pulicaria increased with increasing age (10–30 days). 4. We developed a new method to test for trophic‐level variation in a group of consumers that explicitly accounts for the uncertainty in ΔN. Using this approach, we confirmed that natural assemblages of zooplankton feed at several trophic levels in lake food webs.  相似文献   
72.
Abstract Melittobia are gregarious ectoparasitoid wasps that primarily attack various solitary bees and wasps. Characterized by high levels of inbreeding and an extremely female-biased sex ratio, these wasps appear to satisfy Hamilton's criteria for local mate competition. However, previous studies of sex ratio have failed to take into account an important aspect of Melittobia life history, namely that every clutch represents the combined reproductive output of the initial foundress female plus as many as 37 non-disperser short-winged daughters. Melittobia femorata Dahms is unique among the 13 species of Melittobia in that adults emerge as two temporally distinct clutches. While the overall sex ratio of the combined progeny from both clutches (0.025 ± 0.01) is typical for that for other Melittobia species (between 0.02 - 0.04 for single foundress cultures of the five other species included in this study), the sex ratio for the brachypterous first clutch of M. femorata from field-parasitized hosts averaged about 10 times greater (0.303 ± 0.10). Laboratory experiments with single foundress M. femorata cultures on the same host species ( Trypoxylon politum Say) maintained at 25°C or 30°C produced smaller first clutch sizes compared to the field-infested hosts. While the number of brachypterous first clutch daughters was similar, significantly reduced first clutch sex ratios relative to field-parasitized hosts (0.07 - 0.10) were due to significantly fewer males being produced. Possible reasons for these differences and the elevated first clutch sex ratio in this species are discussed.  相似文献   
73.
The terrestrial carbon cycle plays a critical role in determining levels of atmospheric CO2 that result from anthropogenic carbon emissions. Elevated atmospheric CO2 is thought to stimulate terrestrial carbon uptake, through the process of CO2 fertilization of vegetation productivity. This negative carbon cycle feedback results in reduced atmospheric CO2 growth, and has likely accounted for a substantial portion of the historical terrestrial carbon sink. However, the future strength of CO2 fertilization in response to continued carbon emissions and atmospheric CO2 rise is highly uncertain. In this paper, the ramifications of CO2 fertilization in simulations of future climate change are explored, using an intermediate complexity coupled climate–carbon model. It is shown that the absence of future CO2 fertilization results in substantially higher future CO2 levels in the atmosphere, as this removes the dominant contributor to future terrestrial carbon uptake in the model. As a result, climate changes are larger, though the radiative effect of higher CO2 on surface temperatures in the model is offset by about 30% due to reduced positive dynamic vegetation feedbacks; that is, the removal of CO2 fertilization results in less vegetation expansion in the model, which would otherwise constitute an important positive surface albedo‐temperature feedback. However, the effect of larger climate changes has other important implications for the carbon cycle – notably to further weaken remaining carbon sinks in the model. As a result, positive climate–carbon cycle feedbacks are larger when CO2 fertilization is absent. This creates an interesting synergism of terrestrial carbon cycle feedbacks, whereby positive (climate–carbon cycle) feedbacks are amplified when a negative (CO2 fertilization) feedback is removed.  相似文献   
74.
75.
Fourteen polymorphic microsatellite loci were developed from an enriched genomic library of the widely distributed migratory North American dragonfly species, the common green darner (Anax junius). For a group of 22 larvae, these loci averaged 16 alleles, with individual loci ranging from nine to 29 alleles. Observed heterozygosity averaged 0.784 per locus.  相似文献   
76.
The pattern of solute leakage from imbibing dead pea (Pisumsativum L.) embryos was the same as that from living embryos,with an initially high leakage declining to a low constant rateof leakage in the first 3 min of imbibition. The same patternof leakage occurred during each imbibition phase of repeatedimbibe/dry cycles of dead embryos. Living and dead seeds alsoshowed this pattern of leakage. These observations are usedto argue that leakage during imbibition of embryos and seedsis a physical diffusion phenomenon. Vital staining of livingembryos after imbibition revealed positive staining for dehydrogenaseenzymes in the cells on the outer surface of the cotyledonsonly when 0.5 mM sodium succinate solution was present duringimbibition and/or staining. This is discussed in relation tothe effect of rapid water uptake on these cells.  相似文献   
77.
Five cDNA clones were isolated from barley (Hordeum vulgare L.) that encoded mRNAs related to xyloglucan endotransglycosylase (XET). One of the clones encoded a protein with XET activity in vitro. Sequence comparisons revealed five families of XET-related sequences, one of which (containing two of the barley genes) was novel. Hybridization studies using clone-specific probes indicated that the corresponding genes were represented once, or possibly twice, in the barley genome. Treatment of dwarf mutants with gibberellic acid (GA3), or homozygosity at the ‘slender’ (sln1) locus, resulted in a 2.5-fold (approximately) stimulation of blade elongation rate. Three of the five clones detected mRNAs that were maximally expressed towards the base of the blade, and present in greater quantities in GA3-treated or slender seedlings. The remaining two clones detected mRNAs that were maximally expressed in the middle of the blade. Relative elemental growth rate (REGR) profiles of leaves growing with or without GA3 treatment revealed similar maximal REGR values despite a 2.5-fold difference in leaf elongation rate. Segments of GA3-treated leaves attained their maximal REGR values more rapidly, this being associated with enhanced expression of the three ‘basal’ XET-related mRNAs. Highest XET activities were detected in the base of the elongation zone, and in GA3-treated seedlings a second activity peak was observed near the distal end of the elongation zone. We conclude that there are likely to be several XET isoenzymes with different expression patterns, and identify those XET-related proteins potentially involved in leaf elongation.  相似文献   
78.
Results of the chemical and X-ray analyses are combined to locate the active site and the calcium binding sites.  相似文献   
79.
Within the rosid order Malpighiales, Rhizophoraceae and Erythroxylaceae (1) are strongly supported as sisters in molecular phylogenetic studies and possibly form a clade with either Ctenolophonaceae (2) or with Linaceae, Irvingiaceae and Caryocaraceae (less well supported) (3). In order to assess the validity of these relationships from a floral structural point of view, these families are comparatively studied for the first time in terms of their floral morphology, anatomy and histology. Overall floral structure reflects the molecular results quite well and Rhizophoraceae and Erythroxylaceae are well supported as closely related. Ctenolophonaceae share some unusual floral features (potential synapomorphies) with Rhizophoraceae and Erythroxylaceae. In contrast, Linaceae, Irvingiaceae and Caryocaraceae are not clearly supported as a clade, or as closely related to Rhizophoraceae and Erythroxylaceae, as their shared features are probably mainly symplesiomorphies at the level of Malpighiales or a (still undefined) larger subclade of Malpighales, rather than synapomorphies. Rhizophoraceae and Erythroxylaceae share (among other features) conduplicate petals enwrapping stamens in bud, antepetalous stamens longer than antesepalous ones, a nectariferous androecial tube with attachment of the two stamen whorls at different positions: one whorl on the rim, the other below the rim of the tube, the ovary shortly and abruptly dorsally bulged and the presence of a layer of idioblasts (laticifers?) in the sepals and ovaries. Ctenolophonaceae share with Rhizophoraceae and/or Erythroxylaceae (among other features) sepals with less than three vascular traces, a short androgynophore, an ovary septum thin and severed or completely disintegrating during development, leading to a developmentally secondarily unilocular ovary, a zigzag‐shaped micropyle and seeds with an aril. Special features occurring in families of all three groupings studied here are, for example, synsepaly, petals not retarded and thus forming protective organs in floral bud, petals postgenitally fused or hooked together in bud, androecial tube and petals fusing above floral base, androecial corona, apocarpous unifacial styles, nucellus thin and long, early disintegrating (before embryo sac is mature), and nectaries on the androecial tube. Some of these features may be synapomorphies for the entire group, if it forms a supported clade in future molecular studies, or for subgroups thereof. Others may be plesiomorphies, as they also occur in other Malpighiales or also in Celastrales or Oxalidales (COM clade). The occurrence of these features within the COM clade is also discussed. © 2011 The Linnean Society of London, Botanical Journal of the Linnean Society, 2011, 166 , 331–416.  相似文献   
80.
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