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51.
1. Factors such as reproductive fitness, climatic tolerance, predation pressure, energetic requirements and the quality and quantity of food sources all correlate with invertebrate body sizes. 2. This study examines body size variation between an invertebrate community inhabiting five different microhabitats (mature leaves, new leaves, flowers, fruit and suspended dead wood) that differ in quality, quantity, and availability in an Australian tropical rainforest canopy. 3. Mean body size varied significantly between invertebrate and beetle feeding guilds across microhabitats. Phylogenetically independent contrasts revealed that invertebrate taxonomic groups were significantly smaller on flowers than on mature and new leaves. Size differences between microhabitats were most pronounced among herbivorous taxa (Hemiptera, Lepidoptera). In particular, the immature stages or those groups that develop on flowers were significantly smaller on flowers and larger on leaves than expected. Taxonomic groups with many strong flying species, especially those that complete larval development on resources other than flowers, typically showed no differences in body size across microhabitats. 4. There are a number of potential hypotheses for the smaller body sizes of flower visitors, including: (i) differences in the physical sizes of the microhabitats; (ii) variation in time–dependent mortality risks that influence development times; and (iii) differences in the nutritional quality of the microhabitats, which can influence body size via metabolic pathways. 5. The findings of this study do not support hypothesis (i) (with the possible exception of one or two predatory groups). It is suggested that hypotheses (ii (time–dependent mortality factors) and particularly (iii) (nutritional variation) may be the best avenues for future study as the main drivers of body size differences between microhabitats.  相似文献   
52.
Fire severity is thought to be an important determinant of landscape patterns of post‐fire regeneration, yet there have been few studies of the effects of variation in fire severity at landscape scales on floristic diversity and composition, and none within alpine vegetation. Understanding how fire severity affects alpine vegetation is important because fire is relatively infrequent in alpine environments. Globally, alpine ecosystems are at risk from climate change, which, in addition to warming, is likely to increase the severity and frequency of fire in south‐eastern Australia. Here we examine the effects of variation in fire severity on plant diversity and vegetation composition, 5 years after the widespread fires of 2003. We used floristic data from two wide‐spread vegetation types on the Bogong High Plains: open heathland and closed heathland. Three alternative models were tested relating variation in plant community attributes (e.g. diversity, ground cover of dominant species, amount of bare ground) to variation in fire severity. The models were (i) ‘linear’, attributes vary linearly with fire severity; (ii) ‘intermediate disturbance’, attributes are highest at intermediate fire severity and lowest at both low‐ and high‐severity; and (iii) ‘null’, attributes are unaffected by fire severity. In both heathlands, there were few differences in floristic diversity, cover of dominant species and community composition, across the strong fire severity gradient. The null model was most supported in the vast majority of cases, with only limited support for either the linear and intermediate disturbance models. Our data indicate that in both heathlands, vegetation attributes in burnt vegetation were converging towards that of the unburnt state. We conclude that fire severity had little impact on post‐fire regeneration, and that both closed and open alpine heathlands are resilient to variation in fire severity during landscape scale fires.  相似文献   
53.
Abstract: If individuals can be identified from patterns in their footprints, noninvasive survey methods can be used to estimate abundance. Track plates capture fine detail in the footprints of fishers (Martes pennanti), recording rows of dots corresponding to tiny papillae on the animal's metacarpal pad. We show that the pattern of these dots can be used to identify individual fishers, similar to human fingerprints. A probabilistic model of uniqueness based on variation in spacing between 1,400 pairs of dots that we measured in prints of 14 different fisher feet suggests the probability of encountering a similar pattern in the print of a different foot by chance alone is ≤ 0.35n, where n = the number of dot pairs examined. This predicts a 0.00003 probability that a match made using 10 pairs of dots is false. Dot spacing from footprints made by the same foot was remarkably consistent (sN = 0.02 mm, n = 24 dot pairs). Combined, these results suggest dot patterns in fisher footprints were unique to individuals and were consistently reproduced on track plates. Empirical tests of matching accuracy were best with good-quality prints, highlighting the need for experience judging when prints are usable. We applied print matching to fisher detections collected on track plates deployed at 500-m intervals along 10 3.5-km transects in the Adirondack region of New York, USA. Of 62 fisher detections, 85% had ≥ 1 footprint of suitable quality to compare with other high-quality prints. We found that most detections from a transect were from the same individual fisher suggesting nonindependence of detections. Thus, data from traditional track-plate deployments over small time periods cannot be used as a measure of abundance, but new study designs using print matching could obtain robust noninvasive, mark—recapture density estimates.  相似文献   
54.
A hypothesis on the phylogenetic relationships of the neotropical catfish family Cetopsidae is proposed on the basis of the parsimony analysis of 127 morphological characters and most of the species currently recognized. The family and its two recognized subfamilies, the Cetopsinae and Helogeninae, are corroborated as monophyletic, in agreement with recent studies. Previously proposed classifications of the Cetopsinae, however, were found to be poorly representative of the phylogenetic relationships within the subfamily. Major generic rearrangements are implemented in order that the classification of the Cetopsinae reflects the phylogenetic hypothesis. Pseudocetopsis Bleeker (1862) was found to be polyphyletic and to include several disjunct lineages. One of these lineages, recently named as the genus Cetopsidium Vari, Ferraris, and de Pinna (2005), is the sister group to the rest of the Cetopsinae. Denticetopsis Ferraris (1996) is the next sister group to the remainder of the Cetopsinae. The remaining species of the Cetopsinae belong to one of two sister genera, Paracetopsis Bleeker (1862) and Cetopsis Spix and Agassiz (1829). The latter genus includes species formerly assigned to Hemicetopsis Bleeker (1862), Bathycetopsis Lundberg and Rapp Py‐Daniel (1994) and Pseudocetopsis Bleeker (1862). Continued recognition of Hemicetopsis and Bathycetopsis would have required the creation of several additional new genera for various species previously in Pseudocetopsis that form a series of sister groups to a clade composed of Cetopsis oliveirai (Lundberg and Rapp Py‐Daniel, 1994), C. coecutiens (Lichtenstein, 1819) and C. candiru (Spix and Agassiz, 1829). Cetopsis oliveirai is a highly paedomorphic species that displays surprising similarities with conditions in juvenile specimens of C. coecutiens, a species that attains a large body size. Such similarities are not evident in adult specimens of the latter species. A new classification is proposed, within which the subfamily Cetopsinae consists of three tribes, the Cetopsidiini, the Cetopsini and the Denticetopsini. The results of the study form the basis for a discussion of the phylogenetic position of the family within the Siluriformes, the phylogenetic biogeography of the Cetopsidae, paedomorphosis and gigantism in the family, and the effect of different semaphoronts on the intrafamilial phylogeny. Journal compilation © 2007 The Linnean Society of London, Zoological Journal of the Linnean Society, 2007, 150 , 755–813. No claim to original US government works.  相似文献   
55.
1. A long‐term monitoring programme on phytoplankton and physicochemical characteristics of Esthwaite Water (England) that started in 1945 provides a rare opportunity to understand the effects of climate and nutrients on a lake ecosystem. 2. Monitoring records show that the lake experienced nutrient enrichment from the early 1970s, particularly after 1975, associated with inputs from a local sewage treatment plant, resulting in marked increases in concentration of soluble reactive phosphorus (SRP). Climatic variables, such as air temperature (AirT) and rainfall, exhibit high variability with increasing trends after 1975. 3. Diatom analyses of an integrated 210Pb‐dated lake sediment core from Esthwaite Water, covering the period from 1945 to 2004, showed that fossil diatoms exhibited distinct compositional change in response to nutrient enrichment. 4. Redundancy analysis (RDA) based on diatom and environmental data sets over the past 60 years showed that the most important variables explaining diatom species composition were winter concentrations of SRP, followed by AirT, independently explaining 22% and 8% of the diatom variance, respectively. 5. Additive models showed that winter SRP was the most important factor controlling the diatom assemblages for the whole monitoring period. AirT had little effect on the diatom assemblages when nutrient levels were low prior to 1975. With the increase in nutrient availability during the eutrophication phase after 1975, climate became more important in regulating the diatom community, although SRP was still the major controlling factor. 6. The relative effects of climate and nutrients on diatom communities vary depending on the timescale. RDA and additive model revealed that climate contributed little to diatom dynamics at an annual or decadal scale. 7. The combination of monitoring and palaeolimnological records employed here offers the opportunity to explore how nutrients and climate have affected a lake ecosystem over a range of timescales. This dual approach can potentially be extended to much longer timescales (e.g. centuries), where long‐term, reliable observational records exist.  相似文献   
56.
1. Streams and their adjacent riparian zones are closely linked by reciprocal flows of invertebrate prey. We review characteristics of these prey subsidies and their strong direct and indirect effects on consumers and recipient food webs. 2. Fluxes of terrestrial invertebrates to streams can provide up to half the annual energy budget for drift‐feeding fishes such as salmonids, despite the fact that input occurs principally in summer. Inputs appear highest from closed‐canopy riparian zones with deciduous vegetation and vary markedly with invertebrate phenology and weather. Two field experiments that manipulated this prey subsidy showed that it affected both foraging and local abundance of stream fishes. 3. Emergence of adult insects from streams can constitute a substantial export of benthic production to riparian consumers such as birds, bats, lizards, and spiders, and contributes 25–100% of the energy or carbon to such species. Emergence typically peaks in early summer in the temperate zone, but also provides a low‐level flux from autumn to spring in ice‐free streams. This flux varies with in‐stream productivity, and declines exponentially with distance from the stream edge. Some predators aggregate near streams and forage on these prey during periods of peak emergence, whereas others rely on the lower subsidy from autumn through spring when terrestrial prey are scarce. Several field experiments that manipulated this subsidy showed that it affected the short‐term behaviour, growth, and abundance of terrestrial consumers. 4. Reciprocal prey subsidies also have important indirect effects on both stream and riparian food webs. Theory predicts that allochthonous prey should increase density of subsidised predators, thereby increasing predation on in situ prey and causing a negative indirect effect via apparent competition. However, short‐term experiments have produced either positive or negative indirect effects. These contrasting results may be due to characteristics of the subsidies and individual consumers, but could also result from differences in experimental designs. 5. New study approaches are needed to better determine the direct and indirect effects of reciprocal prey subsidies. Experiments coupled with comparative research will be required to measure their effects on individual consumer fitness and population demographics. Future work should investigate whether reciprocal prey fluxes stabilise linked stream–riparian ecosystems, explore how landscape context affects the magnitude and importance of subsidies, and determine how impacts of human disturbance can propagate between streams and riparian zones via these trophic linkages. Study of these reciprocal connections is helping to define a more holistic perspective of catchments, and has the potential to shape new directions for ecology in general.  相似文献   
57.
The null assumption of molecular variation is that most of it is neutral to natural selection. This is in contrast to variation in morphological traits that we generally assume is maintained by selection, and therefore often by selection coupled to environmental heterogeneity in time and space. Examples of molecular variation that vary over habitat-shifts, particularly in allozymes, show that the relative impact of non-neutral variation as compared to neutral variation might be substantial in some systems. To assess the importance of habitat-generated variation in relation to variation generated by random processes in nuclear DNA markers at small spatial scales, we compared the effects of island isolation and habitat heterogeneity on genetic substructuring in a rocky shore snail ( Littorina saxatilis ). This species has a restricted migration among islands owing to the lack of free-floating larvae. Earlier studies show that allozymes vary extensively as a consequence of isolation by water barriers among islands, but also as a consequence of divergent selection among different microhabitats within islands. In the DNA markers we observed genetic differentiation owing to island isolation at three of nine loci. In addition, variation at three loci correlated with habitat type, but the correlation for two of the loci was weak. Overall, isolation contributed slightly more to the genetic variation among populations than did habitat-related factors but the difference was small. It is concluded that both island isolation, which interrupts gene flow, and a heterogeneous habitat cause genetic substructuring at the DNA level in L. saxatilis in the studied area, and thus in this species we need to be somewhat concerned about habitat heterogeneity also at DNA loci.  © 2004 The Linnean Society of London, Biological Journal of the Linnean Society , 2004, 82 , 377–384.  相似文献   
58.
In order to isolate, clone, and sequence agouti exon 2 of the pig (Yorkshire), we used an interspecific hybridization strategy. Primers from the 5′ and 3′ borders of the known human agouti exon 2 sequence were used to amplify (PCR) pig agouti exon 2. Following Southern blotting using a human exon 2 internal primer to authenticate that our PCR amplified product was truly pig exon 2 (PorAex2), the fragment was cloned and sequenced. PorAex2 exhibits 79.1 and 75.7% DNA sequence and 85 and 74% deduced amino acid sequence homologies with human and mouse agouti exon 2 and agouti protein, respectively. With the isolation of PorAex2, we can now map, sequence, and clarify the modus operandi of the porcine agouti gene. The GenBank Accession number of PorAex 2 is AF018166.  相似文献   
59.
60.
The annual cycle of the White-throated Sparrow, Zonotrichiaalbicollis, is reviewed with brief references to facets of nutritionaland energetic importance (1) illustrating the life of a smallbird in a varying environment, and (2) showing that certainannual events in field populations can be compared with similarmanifestations in caged individuals. Data from captives areemployed in discussions of energetic variations related to (1)food, the source of nutritive input, (2) fat, the major formof caloric storage in birds, and (3) caloric expenditure. Metabolizableenergy is partitioned by phase of the annual cycle into existenceenergy, including the costs of thermoregulation, and productiveenergy, including expenditures for nocturnal activity (Zugunruhe)and molt. Costs of vernal migration in field birds are comparedwith costs of nocturnal activity in captives to show that energeticestimates in each situation are compatible. This conclusionis supported by a metabolic estimate made for field birds thatis within 6% of the estimated metabolism of captives under similarconditions. Data and statistics from seven additional speciesof buntings are used to examine several bioenergetic principlesfor homoiotherms. (1) Minimal metabolism measured by energybalance methods is proportional to the 0.7 power of body weightbut is higher than standard or resting metabolism measured bygaseous methods. (2) Metabolized energy is inversely relatedto ambient temperature below 25°C, the estimated ad libitumcritical temperature. (3) Heat production and loss are proportionatelyhigher in summer-acclimatized birds below the ad libitum criticaltemperature due to reduced insulation. Two summary plots, relatingtemperature, metabolizable energy, and body weight are given.Directions for future research in the study of avian nutritionare suggested.  相似文献   
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