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Allocation of parental investment is predicted to be equal at the population level between both sexes of offspring, and should lead to sex ratio biases in species that exhibit a sex-difference in parental care. Sex-differences in parental care are rarely quantified. We measured daily energy expenditure in free-living nestlings of the extremely sexually size dimorphic European sparrowhawk (Accipiter nisus), using the doubly labelled water method. These data were combined with measured growth characteristics to estimate daily and total metabolised energy intake of male and female young during the nestling stage. Females reached an asymptotic body mass 1.6 times higher than males. This resulted in a total metabolised energy an estimated 1.4 times higher for the nestling stage. Furthermore, we observed a decline in daily metabolised energy with an increase in brood size, which was significantly stronger for females than for males. These results are discussed in the context of Fishers equal allocation theory. Empirical evidence of a sex ratio bias at the end of parental care, with an overall excess of males, is lacking in this species. Consequently, our data do not support the idea of equal allocation between the sexes. The observed sex difference in daily metabolised energy in response to brood size may give scope for sex ratio bias at the level of the individual brood.  相似文献   
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Sexual selection that results in the evolution of exaggerated secondary sexual characters has been hypothesized to impose production and maintenance costs of such traits on their bearers. Costs arising from sexual selection could increase the intensity of predator-mediated natural selection, leading to the prediction that species with exaggerated secondary sexual characters should be particularly susceptible to predation. We tested this prediction in a comparative analysis based on 31,745 prey individuals belonging to 66 species of birds collected from a total of 937 breeding events by 33 to 66 different pairs of European sparrowhawks Accipiter nisus annually during a period of 21 years. To assess vulnerability of different species we estimated a prey vulnerability index based on the difference in the logarithmically transformed absolute abundance of prey minus the logarithmically transformed expected abundance as determined by population density of breeding birds. The prey vulnerability index was predicted by sexual dichromatism, accounting for 23% of the variance in risk of predation among species, even when considering similarity in phenotype among species due to common descent (in the latter case explaining 12% of the variance). This finding suggests that sexual selection is an important evolutionary force-affecting predator–prey interactions.Electronic Supplementary Material Supplementary material is available for this article at  相似文献   
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