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      Positive correlation between genetic diversity and fitness in a large, well-connected metapopulation

      research-article
      1 , , 1 , 2
      BMC Biology
      BioMed Central

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          Abstract

          Background

          Theory predicts that lower dispersal, and associated gene flow, leads to decreased genetic diversity in small isolated populations, which generates adverse consequences for fitness, and subsequently for demography. Here we report for the first time this effect in a well-connected natural butterfly metapopulation with high population densities at the edge of its distribution range.

          Results

          We demonstrate that: (1) lower genetic diversity was coupled to a sharp decrease in adult lifetime expectancy, a key component of individual fitness; (2) genetic diversity was positively correlated to the number of dispersing individuals (indicative of landscape functional connectivity) and adult population size; (3) parameters inferred from capture-recapture procedures (population size and dispersal events between patches) correlated much better with genetic diversity than estimates usually used as surrogates for population size (patch area and descriptors of habitat quality) and dispersal (structural connectivity index).

          Conclusion

          Our results suggest that dispersal is a very important factor maintaining genetic diversity. Even at a very local spatial scale in a metapopulation consisting of large high-density populations interconnected by considerable dispersal rates, genetic diversity can be decreased and directly affect the fitness of individuals. From a biodiversity conservation perspective, this study clearly shows the benefits of both in-depth demographic and genetic analyses. Accordingly, to ensure the long-term survival of populations, conservation actions should not be blindly based on patch area and structural isolation. This result may be especially pertinent for species at their range margins, particularly in this era of rapid environmental change.

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          Most cited references48

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          Landscape modification and habitat fragmentation: a synthesis

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            Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification.

            Simple sequence repeats (SSR), or microsatellites, are ubiquitous in eukaryotic genomes. Here we demonstrate the utility of microsatellite-directed DNA fingerprinting by polymerase chain reaction (PCR) amplification of the interrepeat region. No sequencing is required to design the oligonucleotide primers. We tested primers anchored at 3' or 5' termini of the (CA)n repeats, extended into the flanking sequence by 2 to 4 nucleotide residues [3'-anchored primers: (CA)8RG, (CA)8RY, and (CA)7RTCY; and 5'-anchored primers: BDB(CA)7C, DBDA(CA)7, VHVG(TG)7 and HVH(TG)7T]. Radioactively labeled amplification products were analyzed by electrophoresis, revealing information on multiple genomic loci in a single gel lane. Complex, species-specific patterns were obtained from a variety of eukaryotic taxa. Intraspecies polymorphisms were also observed and shown to segregate as Mendelian markers. Inter-SSR PCR provides a novel fingerprinting approach applicable for taxonomic and phylogenetic comparisons and as a mapping tool in a wide range of organisms. This application of (CA)n repeats may be extended to different microsatellites and other common dispersed elements.
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              Metapopulation dynamics: brief history and conceptual domain

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                Author and article information

                Journal
                BMC Biol
                BMC Biology
                BioMed Central
                1741-7007
                2008
                5 November 2008
                : 6
                : 46
                Affiliations
                [1 ]Biodiversity Research Centre, Université catholique de Louvain, Place Croix du Sud 5, 1348 Louvain-la-Neuve, Belgium
                [2 ]Muséum National d'Histoire Naturelle, Département Ecologie et Gestion de la Biodiversité, CNRS UMR 7179, 4 Avenue du Petit-Château, 91800 Brunoy, France
                Article
                1741-7007-6-46
                10.1186/1741-7007-6-46
                2587462
                18986515
                9829085e-077f-4fba-b29f-5bd6480b824c
                Copyright © 2008 Vandewoestijne et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 25 September 2008
                : 5 November 2008
                Categories
                Research Article

                Life sciences
                Life sciences

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