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      Eco-evolutionary effects on population recovery following catastrophic disturbance

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          Abstract

          Fine-scale genetic diversity and contemporary evolution can theoretically influence ecological dynamics in the wild. Such eco-evolutionary effects might be particularly relevant to the persistence of populations facing acute or chronic environmental change. However, experimental data on wild populations is currently lacking to support this notion. One way that ongoing evolution might influence the dynamics of threatened populations is through the role that selection plays in mediating the ‘rescue effect’, the ability of migrants to contribute to the recovery of populations facing local disturbance and decline. Here, we combine experiments with natural catastrophic events to show that ongoing evolution is a major determinant of migrant contributions to population recovery in Trinidadian guppies ( Poecilia reticulata). These eco-evolutionary limits on migrant contributions appear to be mediated by the reinforcing effects of natural and sexual selection against migrants, despite the close geographic proximity of migrant sources. These findings show that ongoing adaptive evolution can be a double-edged sword for population persistence, maintaining local fitness at a cost to demographic risk. Our study further serves as a potent reminder that significant evolutionary and eco-evolutionary dynamics might be at play even where the phenotypic status quo is largely maintained generation to generation.

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          The Role of Disturbance in Natural Communities

          W P Sousa (1984)
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            Keeping up with a warming world; assessing the rate of adaptation to climate change.

            The pivotal question in the debate on the ecological effects of climate change is whether species will be able to adapt fast enough to keep up with their changing environment. If we establish the maximal rate of adaptation, this will set an upper limit to the rate at which temperatures can increase without loss of biodiversity. The rate of adaptation will primarily be set by the rate of microevolution since (i) phenotypic plasticity alone is not sufficient as reaction norms will no longer be adaptive and hence microevolution on the reaction norm is needed, (ii) learning will be favourable to the individual but cannot be passed on to the next generations, (iii) maternal effects may play a role but, as with other forms of phenotypic plasticity, the response of offspring to the maternal cues will no longer be adaptive in a changing environment, and (iv) adaptation via immigration of individuals with genotypes adapted to warmer environments also involves microevolution as these genotypes are better adapted in terms of temperature, but not in terms of, for instance, photoperiod.Long-term studies on wild populations with individually known animals play an essential role in detecting and understanding the temporal trends in life-history traits, and to estimate the heritability of, and selection pressures on, life-history traits. However, additional measurements on other trophic levels and on the mechanisms underlying phenotypic plasticity are needed to predict the rate of microevolution, especially under changing conditions. Using this knowledge on heritability of, and selection on, life-history traits, in combination with climate scenarios, we will be able to predict the rate of adaptation for different climate scenarios. The final step is to use ecoevolutionary dynamical models to make the link to population viability and from there to biodiversity loss for those scenarios where the rate of adaptation is insufficient.
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              Natural Selection on Color Patterns in Poecilia reticulata

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                Author and article information

                Journal
                Evol Appl
                Evol Appl
                eva
                Evolutionary Applications
                Blackwell Publishing Ltd (Oxford, UK )
                1752-4571
                1752-4571
                March 2011
                : 4
                : 2
                : 354-366
                Affiliations
                [1 ]simpleSchool of Biology and Ecology, University of Maine ME, USA
                [2 ]simpleDivision of Ecology and Evolutionary Biology, University of Glasgow UK
                [3 ]simpleDepartment of Biology, Dalhousie University Halifax, NS, Canada
                [4 ]simpleSchool of Life Sciences, McGill University Montreal, QC, Canada
                Author notes
                Dylan J. Weese, Kellogg Biological Station, Michigan State University, Hickory Corners, MI 49060, USA. Tel.: (269) 671-2534; fax: (269) 671-2104; e-mail: weese@ 123456msu.edu
                Article
                10.1111/j.1752-4571.2010.00169.x
                3352564
                4aa0f3a6-f6f5-4506-9b5c-49ab72adaa76
                © 2011 Blackwell Publishing Ltd
                History
                : 29 September 2010
                : 08 October 2010
                Categories
                Original Article

                Evolutionary Biology
                population dynamics,natural selection and contemporary,sexual selection,population ecology,experimental evolution,evolution,contemporary evolution,population,genetics – empirical,adaptation

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