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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Evolutionary ecology 9 (1995), S. 559-574 
    ISSN: 1573-8477
    Keywords: stochastic demography ; fitness ; life-history ; red deer ; selection pressures ; cost of reproduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Most life-history theory assumes that short-term variation in an organism's environment does not affect the survivorships and fecundities of the organisms. This assumption is rarely met. Here we investigate the population and evolutionary biology of red deer,Cervus elephas, to see if relaxation of this assumption is likely to make significant differences to the predicted evolutionary biology of this species. To do this we used 21 years of data from a population of deer on Rum, Western Isles, Scotland. Population growth rates in a stochastic environment were estimated using Tuljapurkar's small noise approximation, confirmed by bootstrap simulation. Numerical differentiation was used to see if the selection pressures (i.e. sensitivities of population growth rate to changes in the vital rates) differ between the stochastic and deterministic cases. The data also allow the costs of reproduction to be estimated. These costs, incorporated as trade-offs into the sensitivity analysis, allow investigation of evolutionary benefits of different life-history tactics. Environmentally induced stochastic variation in the red deer vital rates causes a slight reduction (≃ 1%) in the predicted population growth rate and has little impact on the estimated selection pressures on the deer's life-history. We thus conclude that, even though density-independent stochastic effects on the population are marked, the deer's fitness is not markedly affected by these and they are adapted to the average conditions they experience. However, the selected life-history is sensitive to the trade-offs between current fecundity, survivorship and future fecundity and it is likely that the environmental variance will affect these trade-offs and, thus, affect the life-history favoured by selection. We also show that the current average life-history is non-optimal and suggest this is a result of selection pressures exerted by culling and predation, now much reduced. As the use of stochastic or deterministic methods provide similar estimates in this case, the use of the latter is justified. Thus,r (the annual per capita rate of population growth) is an appropriate measure of fitness in a population with stochastic numerical fluctuations. In a population of constant size lifetime reproductive success is the obvious measure of fitness to use.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Behavioral ecology and sociobiology 44 (1998), S. 91-98 
    ISSN: 1432-0762
    Keywords: Key words Mate choice ; Sexual selection ; Correlation ; Mate sampling ; Decision rules
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract For intersexual selection to occur, it is necessary that females choose between males. It is now well appreciated that constraints exist, which preclude females sampling all the available males in a population. These constraints are likely to have caused the evolution of sampling rules (such as the “best-of-n” rule) by which females sample males. Here we investigate the impact of female subsampling of the male population, not on the evolution of sampling behaviour, but on the population-level correlation between a male trait and currencies such as reproductive success. This study is important as it illustrates when population-level correlations can be safely used to infer the presence and strength of sexual selection in the field. We find that the correlation between a male trait and a mate choice variable rises steeply as the number of males sampled by each female increases, flattening above seven to ten males sampled. This shape is found to be remarkably robust, and little affected by, for example, the mate choice variable used, by noise in assessment, by sampling behaviour depending on female quality, or by population size. The only variable found to have a large impact is male clumping according to their “quality”. If females are sampling about four males, the maximum correlation that can be found at the population level is in the range 0.4–0.6, perhaps as little as 0.1 if males are strongly clumped. A recent review of the literature suggests that four is the average number of males that females sample. Thus, the absence of a strong correlation cannot by itself be used to infer that sexual selection is weak, as it may be due to females sampling few males.
    Type of Medium: Electronic Resource
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