Graduate Theses & Dissertations

Functional Genetic Diversity in American Mink (Neovison vison)
The release of domestic organisms to the wild is considered a threat to biodiversity because the introduction of domestic genes through interbreeding can negatively impact wild conspecifics via outbreeding and local extinction. In North America, captive American mink (Neovison vison) are frequently escaping into the wild, yet the impact of these events on the functional genetic diversity of wild mink populations is unclear. I characterized domestic and wild mink in Ontario at 17 trinucleotide microsatellites located in functional genes thought to be associated with traits affected by domestication. I found low functional genetic diversity, as only 4 of 17 genes were variable and of those four there was little evidence of allele frequency differences between domestic and wild mink. Using redundancy analysis and a spatial analysis of principal components on the four variable loci (AR, ATN1, IGF-1, and TOB1) I found no evidence to suggest domestic release events are affecting functional genetic diversity of free-ranging mink at the set of markers assessed. Author Keywords: American mink, domestication, functional gene, introgression, Neovison vison
Detection of four at-risk freshwater pearly mussel species (Bivalvia
Environmental DNA (eDNA) detection uses species-specific markers to screen DNA from bulk samples, such as water, to infer species presence. This study involved the development and testing of species-specific markers for four freshwater pearly mussels (Unionidae). The markers were applied to water samples from intensively sampled mussel monitoring sites to compare species detections from eDNA with established sampling method detections. Target species were detected using eDNA at all sites where they had previously been detected by quadrat sampling. This paired design demonstrated that eDNA detection was at least as sensitive as quadrat sampling and that high species specificity can be achieved even when designing against many sympatric unionids. Detection failures can impede species conservation efforts and occupancy estimates; eDNA sampling could improve our knowledge of species distributions and site occupancy through increased sampling sensitivity and coverage. Author Keywords: conservation genetics, cytochrome oxidase subunit I (COI), environmental DNA (eDNA), quantitative PCR (qPCR), species at risk (SAR)

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