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P O'Donald

Publications and source records attributed to P O'Donald.

At least 19 recordsLinked to original sources

Frequency-dependent sexual selection.

Sexual selection by female choice is expected to give rise to a frequency-dependent sexual advantage in favour of preferred male phenotypes: the rarer the preferred phenotypes, the more often they are chosen as mates. This 'rare-male advantage' can maintain a polymorphism when two or more phenotypes are mated preferentially: each phenotype gains an advantage when it is rarer than the others; no preferred phenotype can then be lost from the population. Expression of preference may be complete or partial. In models of complete preference, females with a preference always mate preferentially. Models of partial preference are more realistic: in these models, the probability that a female mates preferentially depends on the frequency with which she encounters the males she prefers. Two different 'encounter models' of partial preference have been derived: the O'Donald model and the Charlesworth model. The encounter models contain the complete preference model as a limiting case. In this paper, the Charlesworth model is generalized to allow for female preference of more than one male phenotype. Levels of frequency dependence can then be compared in the O'Donald and Charlesworth models. The complete preference model and both encounter models are formulated in the same genetical terms of preferences for dominant and recessive male phenotypes. Polymorphic equilibria and conditions for stability are derived for each of the three models. The models are then fitted to data of frequencies of matings observed in experiments with the two-spot ladybird. The complete preference model gives as good a fit as the encounter models to the data of these and other experiments. The O'Donald and Charlesworth encounter models are shown to produce a very similar frequency-dependent relation. Generally, as females become less choosy, they express their preference with more dependence on male frequency, whereas the resulting selection of the males becomes less frequency dependent. More choosy females are more constant in expressing their preference, producing greater frequency dependence in the selection of the males.

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Sexual selection and fertility.

Genetic models are analyzed in which sexual selection is combined with fertility selection. In these models, the sexual selection acts on males, the fertility selection on either males, females or both sexes. The phenotypes thus selected may be determined either by dominant and recessive alleles or by each homozygous and heterozygous genotype. Polymorphisms of dominant and recessive phenotypes can be maintained in equilibrium by a balance between sexual and fertility selection. Generally fertility selection has a greater effect than viability selection in determining the point of equilibrium. The dominant phenotype is maintained at a lower frequency when at a fertility disadvantage than when at a viability disadvantage. When about 20% or more of the females mate preferentially, the models show that equilibria will be established at very different frequencies depending on whether fertility selection acts on males, females or both sexes. These results, applied to data of preferential mating of melanic two-spot ladybirds, predict differences in fertility which can be use to test the models. Symmetric models of preferences for each genotype also give rise to polymorphisms if the heterozygotes obtain an overall advantage.

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A general analysis of genetic models with frequency-dependent mating. II. Sexual selection for heterozygotes.

Heterozygotes are assumed to mate with a frequency that is any general function, f(v), of their population frequency, v. Models are analysed in which the selection that determines the function f(v) acts either on one sex alone or on both sexes equally. The central equilibrium point v* = 1/2 always exists; it is stable if f(1/2) greater than 1/2. If the central equilibrium is unstable, other asymmetric equilibria may be stable; the fixation states may also be stable. This general analysis is applied to a number of specific models of sexual selection. The models give qualitatively different results. The outcome of selection in population cage experiments could be used to test the alternative models.

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Estimation of assortative mating preferences in the Arctic skua.

Methods are described for the maximum likelihood estimation of mating preferences in models of assortative mating for monogamous and polygamous organisms. These methods are applied to data of matings of the three phenotypes, pale, intermediated and dark of the Arctic Skua. The data were obtained by exhaustive surveys of the Arctic Skua populations on the islands of Fair Isle and Foula. The data give evidence of significant assortative mating of pale birds on Foula and intermediate birds on Fair Isle. The combined data show that there is very highly significant assortative mating, but only of intermediates. In previous surveys, data, in which intermediates and darks were not distinguished, were obtained from a number of islands in the Shetlands. These data, combined with the present data, show that the overall assortative mating of pale is very highly significant with no evidience of heterogeneity. The assortative mating of intermediate birds on Fair Isle agrees with other evidence showing that inermediate males have an advantage as a result of sexual selection.

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A demographic analysis of the components of selection in a population of Arctic Skuas.

From previously published demographic data of the age distributions and reproductive rates of the pale, intermediate and dark phenotypes of the Arctic Skua, revised estimates are obtained of the intrinsic rates of increase and selective coefficients of the phenotypes in each sex. Two significant components of selection are variation in age of maturity and variation in reproductive success. Sexual selection is a component of the variation in reproductive success. Dark and intermediate birds have a greater reproductive success than pales, partly as a result of their advantage in sexual selection. Pale birds have an overall advantage, however, because they are younger when they first breed. Given the estimated selective coefficients, a computer model predicts that pale birds will gradually replace the others. So far there are not enough data collected over a sufficiently long time to test the model rigorously.

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