16 research outputs found

    Location and assignment to genetic clusters of ten subpopulations of <i>Phelsuma guimbeaui</i>.

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    <p><b>a</b> Subpopulations used for the microsatellite analyses. Colours in the pie charts indicate the proportion of genetic clusters identified using STRUCTURE 2.3.2. The three subpopulations only used for mtDNA analyses (L11, L12 and L13) are also shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0093387#pone-0093387-g002" target="_blank">Figure 2a</a>; subpopulations marked with an asterisk are in the Black River mountains. <b>b</b> Bar plots showing the genetic identity of individual samples generated using STRUCTURE 2.3.2. <b>c</b> Bar plot output from TESS with each subpopulation's labelling assignment (%) from GENECLASS2 shown below. The box gives details of each subpopulation (Subpop): vegetation (Veg) was classified as exotic campeche forest (C), exotic eucalyptus forest (E), exotic mango orchard (M), native forest (N) and exotic terminalia forest (T); size is the area (km<sup>2</sup>) occupied by each subpopulation.</p

    Phylogenetic relationships of mtDNA haplotypes in <i>Phelsuma guimbeaui</i>.

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    <p>The Bayesian tree was produced in MRBAYES with subpopulation identity (L1 to L13) shown at the end of each branch. In the parsimony network, the circles represent different haplotypes, with their size proportional to the number of geckos. Open circles represent predicted but missing or unsampled haplotypes.</p

    Population statistics of the concatenated mtDNA sequences for 13 subpopulations of <i>Phelsuma guimbeaui</i>.

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    <p>* denotes significant at P<0.05.</p><p>Subpop = subpopulation; Area = area of subpopulation in km<sup>2</sup>; A = number of individuals per subpopulation; H<sub>N</sub> = number of haplotypes; H = haplotype diversity; π = nucleotide diversity; D = Tajima's D; Fs = Fu's Fs statistic; r = raggedness index.</p

    Pattern of deforestation in Mauritius from 1773 to 1997.

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    <p>The red dots indicate the 10 subpopulations for which both microsatellite and mtDNA analyses were conducted, and the yellow dots the three subpopulations for which only mtDNA analyses were carried out. The blue stars mark subpopulations not sampled and the black region within the purple dotted line on the 1997 map shows the Black River mountains. All subpopulation locations were transposed by 1</p

    Population genetic indices (± standard deviation) for ten subpopulations of <i>Phelsuma guimbeaui</i>.

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    <p>Subpop = subpopulation; A = number of individuals sampled; H<sub>E</sub> = mean expected heterozygosity and standard deviation; H<sub>O</sub> = mean observed heterozygosity and standard deviation; N<sub>A</sub> = mean number of alleles and standard deviation; A<sub>R</sub> = mean allelic diversity and standard deviation; P<sub>A</sub> = mean private allelic richness and standard deviation; F<sub>IS</sub> = inbreeding coefficient. N<sub>A</sub>, A<sub>R</sub> and P<sub>A</sub> were based on a minimum sample of 22 geckos per subpopulation.</p

    Ecological Effects of the Invasive Giant Madagascar Day Gecko on Endemic Mauritian Geckos: Applications of Binomial-Mixture and Species Distribution Models

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    <div><p>The invasion of the giant Madagascar day gecko <i>Phelsuma grandis</i> has increased the threats to the four endemic Mauritian day geckos (<i>Phelsuma</i> spp.) that have survived on mainland Mauritius. We had two main aims: (i) to predict the spatial distribution and overlap of <i>P. grandis</i> and the endemic geckos at a landscape level; and (ii) to investigate the effects of <i>P. grandis</i> on the abundance and risks of extinction of the endemic geckos at a local scale. An ensemble forecasting approach was used to predict the spatial distribution and overlap of <i>P. grandis</i> and the endemic geckos. We used hierarchical binomial mixture models and repeated visual estimate surveys to calculate the abundance of the endemic geckos in sites with and without <i>P. grandis</i>. The predicted range of each species varied from 85 km<sup>2</sup> to 376 km<sup>2</sup>. Sixty percent of the predicted range of <i>P. grandis</i> overlapped with the combined predicted ranges of the four endemic geckos; 15% of the combined predicted ranges of the four endemic geckos overlapped with <i>P. grandis</i>. Levin's niche breadth varied from 0.140 to 0.652 between <i>P. grandis</i> and the four endemic geckos. The abundance of endemic geckos was 89% lower in sites with <i>P. grandis</i> compared to sites without <i>P. grandis</i>, and the endemic geckos had been extirpated at four of ten sites we surveyed with <i>P. grandis</i>. Species Distribution Modelling, together with the breadth metrics, predicted that <i>P. grandis</i> can partly share the equivalent niche with endemic species and survive in a range of environmental conditions. We provide strong evidence that smaller endemic geckos are unlikely to survive in sympatry with <i>P. grandis</i>. This is a cause of concern in both Mauritius and other countries with endemic species of <i>Phelsuma</i>.</p></div
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