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  • habitat selection  (2)
  • Springer  (2)
  • American Institute of Physics (AIP)
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  • Springer  (2)
  • American Institute of Physics (AIP)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Evolutionary ecology 1 (1987), S. 315-330 
    ISSN: 1573-8477
    Keywords: Coevolution ; density-dependent fitnesses ; fitness sets ; habitat selection ; isolegs ; specialization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Question: What are the conditions required for natural selection to produce phenotypes specially adapted to the various habitats available in nature? Model: Assume there are two habitat types and one or two phenotypes of the same or different species. The phenotypes do not recognize any spatial differences among patches of the same habitat type. Possible evolutionary winners can do better in one habitat only by relinquishing some ability in the other. Results: If only one phenotype is present, it will be an intermediate (unless one of the two habitat types is so rare and unproductive that its effects can be ignored by natural selection). Even if two phenotypes are introduced, natural selection should generally restore monomorphism if habitat selection is not ever favored (e.g. if search costs are high). But if search costs and environmental variation are zero, dimorphism can be expected. And if they are small, then although monomorphism is stable, its basin of attraction is small, and invasion by a second form (such as a sibling species) can provide the discontinuous jump needed to put the system in the other basin of attraction. Once there, dimorphic extremism coevolves. Each successful morph is as specialized as possible on one of the habitats. Competition between the morphs is eliminated. Environmental variation may constrict the basin, but once a point is captured by it, the system approaches dimorphic extremism anyway. In general, whatever promotes the behavior of habitat selection also promotes the evolution of extreme morphologies and physiologies.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Evolutionary ecology 11 (1997), S. 733-756 
    ISSN: 1573-8477
    Keywords: optimal foraging ; gerbil ; competition ; predation ; mutualism ; habitat selection ; dipswitch theory ; community ecology ; isocline ; isoleg ; population dynamics ; interaction coefficient ; density dependence ; ideal free distribution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Optimal foraging theory has entered a new phase. It is not so much tested as used. It helps behavioural ecologists discover the nature of the information in an animal's brain. It helps population ecologists reveal coefficients of interaction and their patterns of density-dependent variation. And it helps community ecologists examine niche relationships. In our studies on two species of Negev desert gerbil, we have taken advantage of the second and third of these functions. Both these gerbils prefer semi-stabilized dune habitat, and both altered their selective use of this habitat and stabilized sand according to experimental changes we made in their populations. Their changes in selectivity agree with a type of optimal foraging theory called ‘isoleg theory’. Isoleg theories provide examples of dipswitch theories – bundles of articulated qualitative predictions – that are easier to falsify than single qualitative predictions. By linking behaviour to population dynamics through isoleg theory, we were able to use the behaviour of the gerbils to reveal the shapes of their competitive isoclines. These have the peculiar non-linear shapes predicted by optimal foraging theory. Finally, when owl predation threatens, the behaviour of Gerbillus allenbyi reveals the shape of their victim isocline. As has long been predicted by predation theory and laboratory experiments, it is unimodal.
    Type of Medium: Electronic Resource
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