Thesis (M.A.)--York University, 2005. Graduate Programme in Art History. / Typescript. Includes bibliographical references (leaves 104-113). Also available on the Internet. MODE OF ACCESS via web browser by entering the following URL: http://gateway.proquest.com/openurl?url%5Fver=Z39.88-2004&res%5Fdat=xri:pqdiss &rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:MR11811

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In 1970 the Arrow oil spill off Cape Breton contaminated 305 kilometres of shoreline. Aerial and land surveys have demonstrated that natural weathering has occurred throughout this period, but it was relatively slow, especially in sheltered areas like Black Duck Cove lagoon. This study analyzed the microbial hydrocarbon degradation potential in the lagoon sediments using direct and culture-based techniques. Mineralization of hydrocarbon substrates (hexadecane, octacosane and naphthalene) indicated the presence of an active degradative microbial community, however, genes from known bacterial hydrocarbon degradation pathways (alkB, ndoB, phnAc) were not detected by direct extraction of sediment DNA and PCR amplification. Sediment enrichment cultures had increased mineralization rates for naphthalene and hexadecane, and a hexadecane-degrading pure culture, Rhodococcus sp. BDC14, with a typical alkB gene was isolated. PCR analysis of total community DNA extracted directly from the enrichments indicated the presence of the Alcanivorax borkumensis alkB1 genotype. The results demonstrated that there were notable differences between culture-based and direct molecular analytical techniques in characterizing the contaminated sediments.

Methylmercury (MeHg) is the most toxic form of Hg to wildlife, partly because of its ability to biomagnify through the food chain. Previous studies have shown that river otter (Lutra canadensis) is particularly susceptible to increased exposure and body burdens of MeHg due to the piscivorous nature of its diet. The objectives of this study were to attempt to establish a relationship between MeHg concentrations in otter tissues and DNA fragmentation using single cell electrophoresis (comet assay) as well as evaluate the effectiveness of the comet assay as a tool in genotoxicity assessment in field samples. Results of preliminary experiments indicate that both time and storage temperature markedly influence the rate of spontaneous DNA degradation. Increased numbers of freeze/thaw cycling also appear to have a negative effect on DNA integrity. In addition, a cell culture experiment was set up to measure the effects of differing levels of MeHg on a neuroblastoma cell line.

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