2013
DOI: 10.1007/s10592-013-0521-8
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Population genetics of Blanding’s turtle (Emys blandingii) in the midwestern United States

Abstract: Blanding's turtle (Emys blandingii) has declined substantially in North America due to anthropogenic activities, leaving populations smaller and increasingly fragmented spatially. We sampled 212 turtles to evaluate variation at eight microsatellite loci within and among 18 populations of E. blandingii across its primary range in the midwestern United States (Illinois, Iowa, Minnesota, and Nebraska). All loci and populations were highly polymorphic. Our analyses also detected considerable genetic structure with… Show more

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Cited by 19 publications
(18 citation statements)
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References 59 publications
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“…Extremely high genetic differentiation between populations of a single species is unusual, although similar levels have been documented over large geographic scales in sponges (Chaves-Fonnegra et al, 2015), coastal sharks (Ashe et al, 2015) and marine mammals (Fruet et al, 2014), but also at distances o100 km in terrestrial animals (Sethuraman et al, 2013) or freshwater diatoms (Vanormelingen et al, 2015). Our results indicate that the populations of L. brevirostris α present clear geographic boundaries and are consistent with two of the characteristics of a metapopulation model (Grimm et al, 2003): (1) local populations have their own dynamics and (2) they are connected by limited dispersal.…”
Section: Discussionmentioning
confidence: 69%
“…Extremely high genetic differentiation between populations of a single species is unusual, although similar levels have been documented over large geographic scales in sponges (Chaves-Fonnegra et al, 2015), coastal sharks (Ashe et al, 2015) and marine mammals (Fruet et al, 2014), but also at distances o100 km in terrestrial animals (Sethuraman et al, 2013) or freshwater diatoms (Vanormelingen et al, 2015). Our results indicate that the populations of L. brevirostris α present clear geographic boundaries and are consistent with two of the characteristics of a metapopulation model (Grimm et al, 2003): (1) local populations have their own dynamics and (2) they are connected by limited dispersal.…”
Section: Discussionmentioning
confidence: 69%
“…() found similar levels of heterozygosity between co‐distributed E. blandingii and C. serpentina in Wisconsin, USA. Overall, estimates of heterozygosity for C. picta (0.68–0.82; Laporte, Beaudry & Angers, ; Jensen, Govindarajulu & Russello, ; Reid et al ., ) and C. serpentina (0.57–0.67; Davy, ; Reid et al ., ) were comparable to previous studies, whereas reported heterozygosity varied substantially among E. blandingii across the Midwest (0.38–0.80; Mockford et al ., ; Klut, ; McGuire, Scribner & Congdon, ; Sethuraman et al ., ; Reid et al ., ). Furthermore, our diversity estimates for C. guttata in Illinois were depressed compared to populations in Ontario, Canada (0.67; Davy & Murphy, ) and potentially correspond to genetic drift experienced by the peripheral Illinois sites.…”
Section: Discussionmentioning
confidence: 99%
“…For both genetic diversity metrics, on the other hand, roads were a better predictor of variability than public land area, with models containing only road density weighted 3 times higher (for allelic richness) or 27 times higher (for heterozygosity) than models containing public land area alone. While a number of studies have assessed microsatellite genetic variability at regional scales in E. blandingii (Mockford et al ., ; Davy et al ., ; Sethuraman et al ., ), none have explicitly examined the effects of land use on genetic diversity. Continuing loss of individuals of either sex causes loss of genetic diversity over time (Jackson & Fahrig, ) and additional effects of habitat fragmentation (such as reduced gene flow) will likely compound this effect (Keyghobadi ), meaning that genetic diversity may be more sensitive to persistent low levels of road mortality than sex ratio.…”
Section: Discussionmentioning
confidence: 99%