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Diplotaxini Kirby is one of the 29 tribes of Melolonthinae with Nearctic, Neotropical, Paleartic, Afrotropical and Oriental distribution. According to the current classification, Diplotaxini is composed of 706 species described in 21 genera. Neotropical Diplotaxini comprise 94 species, of which 78 are members of Liogenys Guérin Méneville, the largest Neotropical genus. Until now, no phylogenetic studies on Diplotaxini have tested whether the tribe is natural or artificial. This study tested the relationships among Diplotaxini genera, created hypotheses for better defining them, and assessed the monophyly of Liogenys. Cladistic analyses using 167 adult morphological characters were performed. The 83 included taxa represent three subfamilies of Melolonthidae, four tribes of Melolonthinae, and most genera of Diplotaxini, with emphasis on Liogenys. The data were analysed using parsimony under equal and implied weights. In both analyses, the traditional concept of Diplotaxini is shown to be a polyphyletic assemblage. Empecta Erichson and Clypeasta Fairmaire are closely related to Melolontha melolontha (Linnaeus) and Pseudoliogenys Moser close to Myloxenoides Martínez (Tanyproctini). Pachrodema Blanchard is identified as the sister group of Liogenys. The monophyly of both Pacuvia Curtis and Homalochilus Blanchard is confirmed and the paraphyly of Diplotaxis Kirby is suggested. The analyses strongly supported the polyphyly of Liogenys. To render this genus monophyletic, we transferred L. ferrugata Mannerheim (related to M. melolontha) to Phyllophaga Harris, and L. micropyga Burmeister to Diplotaxis, forming Diplotaxis micropyga (Burmeister, 1855) comb.n. ; and included Homoliogenys tarsalis (Moser) and Hilarianus anguliceps Blanchard in Liogenys. As H. anguliceps is syn. junior of Liogenys punctaticollis, Hilarianus is synonymized with Liogenys. Hilarianus ovalis and Hilarianus rufinus are here assigned to Manonychus, and Hilarianus uniformis and Hilarianus suboblongus to Blepharotoma, forming: Blepharotoma uniformis comb.n. , Blepharotoma suboblongus comb.n. , Manonychus ovalis comb.n. and Manonychus rufinus comb.n.  相似文献   
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Biogeographical patterns of animal body size and the environmental and evolutionary mechanisms that may be driving them have been broadly investigated in macroecology, although just barely in ectotherms. We separately studied two snake clades, Viperidae and Elapidae, and used phylogenetic eigenvector regression and ordinary least squares multiple regression methods to perform a global grid-based analysis of the extent at which the patterns of body size (measured for each species as its log10-transformed maximum body length) of these groups are phylogenetically structured or driven by current environment trends. Phylogenetic relatedness explained 20% of the across-species size variation in Viperidae, and 59% of that of Elapidae, which is a more recent clade. Conversely, when we analysed spatial trends in mean body size values (calculated for each grid-cell as the average size of its extant species), an environmental model including temperature, precipitation, primary productivity (as indicated by the global vegetation index) and topography (range in elevation) explained 37.6% of the variation of Viperidae, but only 4.5% of that of Elapidae. These contrasted responses of body size patterns to current environment gradients are discussed, taking into consideration the dissimilar evolutionary histories of these closely-related groups. Additionally, the results obtained emphasize the importance of the need to start adopting deconstructive approaches in macroecology.  © 2009 The Linnean Society of London, Biological Journal of the Linnean Society , 2009, 98 , 94–109.  相似文献   
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Vibrational communication is important for successful mating in various stink bugs species. The vibrational signals from males and females of Dichelops melacanthus Dallas (Hemiptera: Pentatomidae) are recorded from a nonresonant substrate (i.e. a loudspeaker membrane) to characterize the temporal and spectral properties of these vibrational signals, as well as on a resonant substrate (i.e. bean plants) to obtain information about how these signals are altered when they are transmitted through the plants. On the loudspeaker membrane, D. melacanthus males and females emit only one male or one female song, respectively. However, when the insects are placed on bean leaves, a more complex repertoire is recorded, with three different songs for each sex. The first female and male songs appear to have calling functions and the third male and female songs are emitted during courtship. The second female and male songs are emitted after the first song, although their functions in mating behaviour are not clear. The identified repertoire is similar to those of other Neotropical stink bugs, starting with songs 1 and 2 and developing into song 3. Frequency modulation is observed in the female songs recorded from the loudspeaker membrane and the plants. The signals recorded from plants present higher harmonic peaks compared with the signals recorded from the loudspeaker membrane. The presence of species and sex‐specific songs during mating confirms the important role of vibrational communication in mate location and recognition. The temporal and spectral characteristic signals are influenced by the substrate used to record the songs emitted by D. melacanthus.  相似文献   
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1. The European freshwater pearl mussel, Margaritifera margaritifera (Bivalvia: Unionoida), is one of the most threatened mussels. The Iberian populations of this species are considered peripheral because their distinct characters such as growth rate and longevity, and require development of effective conservation strategies. 2. We assessed population density and age structure of pearl mussels in two Galician rivers (Eo and Masma in north‐west Spain). Four sampling sites were selected in each river to cover stretches of 100 m. The mean density of mussels in each of these sampling transects was estimated using the adaptive sampling technique, given that mussels occur at low densities and are highly aggregated in these rivers. 3. Age structure was inferred for each population using length–age keys. The empty shells encountered during sampling were used to determine the length of the specimens at different ages (years), together with length‐at‐age data from shells previously analysed for computing growth rates from the same rivers. Water samples from both rivers were analysed for typical physicochemical parameters. 4. Mean densities were very variable, even within the same river (from 0.27 to 6.55 m?2 in the River Eo and from 0.98 to 2.38 m?2 in the River Masma). Individuals in the 0‐ to 5‐year age class were scarce in both rivers. 5. Margaritifera margaritifera showed a preference for the strip of river bed within 1.5 m from the river bank and avoided sites at greater distances. The species also showed a preference for sites with more than 80% tree cover and avoided sites with <50% cover. 6. Iberian populations exhibit the highest growth rate, together with the lowest maximum age and maximum length known for M. margaritifera. Detailed knowledge about these peripheral Iberian populations will contribute to developing strategies for conservation and management of this endangered species.  相似文献   
138.
Phylogeographic studies from western Palaearctic have generally focused on species able to disperse and track their emerging suitable habitats after the last ice age. However, data on species whose biogeographical histories differ from this bulk of Palaearctic fauna are scarce. This is clearly the case of some specialized organisms inhabiting inland hypersaline environments, which are likely to have had a wider distribution range during the late Tertiary and may have persisted through the Pleistocene to the present day only constituting relict populations. In this study, we use partial sequences from two mitochondrial genes [16S rRNA (16S) and cytochrome oxidase subunit II (COII)] to investigate the phylogeography of the Iberian populations of Mioscirtus wagneri (Orthoptera: Acrididae), a specialized grasshopper exclusively inhabiting hypersaline low grounds. Our results show that M. wagneri exhibits a marked phylogeographical structure, forming three main clades which correspond with populations located in north-east, central–south-east and south-west Iberia. These geographical areas did not share any haplotype, indicating that gene flow between them is absent. Nested clade analyses revealed that these lineages have probably evolved in allopatry and data on sequence divergence suggest population fragmentation from the Early Pleistocene. Overall, these results provide a broader perspective on the contribution of historical climate/geological events to biogeographical patterns of organisms currently forming relict populations of great conservation concern.  © 2009 The Linnean Society of London, Biological Journal of the Linnean Society , 2009, 97 , 623–633.  相似文献   
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The sensitivity of the original versus the modified Salmonella-Tek enzyme immunoassay (EIA) was compared for recovery of Salmonella spp. from selected low-moisture foods. Serial tenfold dilutions were inoculated into incubated post enrichment media (dilution-to-extinction approach). Results indicated no significant difference between the original and modified Salmonella-Tek EIAs. A comparison of the modified Salmonella-Tek EIA and the modified GENE-TRAK Salmonella assay, using the same approach, also showed no significant differences.
The effectiveness of the assays was then compared using a second approach (dry bulk inoculation). A lyophilized culture was inoculated into bulk food. Replicate 25-g test portions were used in a 3-way comparison of the effectiveness of the modified Salmonella-Tek EIA, the modified GENE-TRAK Salmonella assay, and the standard culture method approved by the Association of Official Analytical Chemists (AOAC) International and recommended in the Food and Drug Administration's Bacteriological Analytical Manual. Of 460 test portions examined, 307 gave positive reactions with the modified Salmonella-Tek EIA, 298 with the modified GENE-TRAK Salmonella assay, and 292 with the AOAC/BAM culture method.  相似文献   
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