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  • Sperm competition  (1)
  • aggression  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of mathematical biology 39 (1999), S. 91-108 
    ISSN: 1432-1416
    Keywords: Key words: Evolutionarily stable strategies ; Game theory ; Sperm competition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract.  In principle there are two approaches to modelling a trade-off between the positive and negative outcomes of a behavior: after suitably defining a value for the behavior in the absence of any trade-off, one can either multiply that value by an appropriate discount or subtract an appropriate cost. In a prospective analysis of sperm competition, Parker (Proc. Roy. Soc. Lond. B (1990) 242, 120–126) adopted the multiplicative approach to model the trade-off between the value of a mating and the cost of its acquisition. He obtained two paradoxical results. First, if two males ‘know’ whether they are first or second to mate, but these roles are assigned randomly, then sperm numbers should be the same for both males whether the ‘raffle’ for fertilization is fair or unfair. Second, if mating order is constant, then a favored male should expend less on sperm. His results are puzzling not only in terms of intuition about nature, but also in terms of his model’s consistency. In other words, they present both an external and an internal paradox. Parker assumed the fairness of the raffle to a disfavored male to be independent of how much sperm a favored male deposits. This article both generalizes Parker’s analysis by allowing fairness to decrease with sperm expenditure by the favored male and compares Parker’s results to those obtained by the additive approach. In many respects, results are similar. Nevertheless, if the costs of mating are assumed to increase with sperm expenditure but not to depend on the role in which sperm is expended, as Parker assumed, then the additive approach is more fundamentally correct. In particular, Parker’s constant-role paradox is an artifact of his approach. His random-role paradox is internally rationalized in terms of standard microeconomic theory. When fairness decreases, however slightly, with sperm expenditure by the favored male, both models demonstrate that the evolutionarily stable strategy is for more sperm to be deposited during a favored mating than during a disfavored mating. The lower the costs, the greater the divergence. Thus a possible resolution of the external paradox is that fairness is not constant in nature.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-8477
    Keywords: ESS ; game theory ; aggression ; resource holding potential ; beetles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The classic Hawk—Dove game is extended to deal with continuous variation in resource-holding potential or RHP, when RHP is observable (via any sensory modality) but RHP difference is less than perfectly reliable as a predictor of the outcome of an escalated contest. The relationship between sensory and physical magnitudes of RHP is assumed to be governed by Fechner's psychophysical law, whose effect is that contestants interact as if they had perfect information about their relative RHP (as opposed to RHP difference). Thus, an animal is aggressive if its RHP exceeds a certain fraction, called its threshold, of its opponent's RHP and otherwise is non-aggressive; and the classic Hawk and Dove strategies correspond to zero and infinite thresholds, respectively. For RHPs drawn at random from an arbitrary Gamma distribution there is a unique evolutionarily stable strategy or ESS, which depends on a parameter α measuring the reliability of RHP as a predictor of the outcome of a fight, on the ratio of the valueV of winning to the costC of losing (both measured in units of reproductive fitness) and on the mean µ and variance σ2 of the RHP distribution. In a population at this ESS, ifV/C 〈 1 then the threshold is 1 and there is no fighting. AsV/C increases beyond 1 to a second critical value ζ, however, the threshold decreases steadily from 1 to 0 and remains 0 forV/C 〉 ζ; ζ is an increasing function of α, but a decreasing function of σ2. That a lower variance of RHP can imply a lower escalation frequencyp is a novel insight of the analysis. The prediction is at first counterintuitive, because if the aggression threshold were fixed then larger variance would imply lowerp (dispersion effect of variance). When natural selection acts on the threshold, however, increasing the variance not only reduces the probability that an animal with larger RHP will be attacked by an animal with lower RHP at the existing threshold, but also reduces the expected costs of adopting that particular threshold, so that a mutant with a somewhat lower threshold can invade the population (selection effect of variance). Forp, the selection effect dominates toward the upper end of the interval 1 ≤V/C ≤ ζ.
    Type of Medium: Electronic Resource
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