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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
11

Studies on the population genetics of Euphausiids: a comparison of patterns in plagic taxa displaying different distributions and life-histories.

Harkins, Gordon W January 2006 (has links)
<p>The systematic and population genetic relationships were characterised for three ecologically related euphausiid species: Euphausia lucens, E. recurva and E. vallentini. These species have different geographical distributions and life histories. All three species have a circumpolar distribution in the Southern Hemisphere while E. recurva is also distributed in the North Pacific. DNA sequence variation was determined for three regions of mitochondrial DNA and a single nuclear gene. It was conclusively demonstrated that both E. lucens and E. vallentini represent valid taxonomic species with fixed differences observed in both the nuclear and mitochondrial genes and that the low divergences previously reported for these species with 16SrRNA and CO1 resulted from a species misidentification. It was also shown that previous attempts to date the divergence between Antarctic and Sub-Antarctic euphausiid species based on 16SrRNA distances suffer from a large overestimation due to a calculation error.</p>
12

Conservation genetics of the Eurasian otter in Sweden /

Arrendal, Johanna, January 2007 (has links)
Diss. (sammanfattning) Uppsala : Univ., 2007. / Härtill 5 uppsatser. Med sammanfattning på svenska.
13

Phylogeography and population genetic structure of double-crested cormorants (Phalacrocorax auritus) /

Mercer, Dacey M. January 1900 (has links)
Thesis (M.S.)--Oregon State University, 2009. / Printout. Includes bibliographical references. Also available on the World Wide Web.
14

Habitat fragmentation, functional landscape connectivity, and metapopulation processes in amphibians

Greenwald, Katherine R., January 2009 (has links)
Thesis (Ph. D.)--Ohio State University, 2009. / Title from first page of PDF file. Includes vita. Includes bibliographical references (p. 82-92).
15

The selective and demographic history of Drosophila melanogaster

Ometto, Lino, January 2006 (has links)
Thesis (doctoral)--Ludwig-Maximilians-Universität München, 2006. / Title from PDF t.p. (viewed on May 13, 2006). Includes bibliographical references.
16

Population Structure of Island-Associated Pantropical Spotted Dolphins (Stenella attenuata) in Hawaiian Waters

Courbis, Sarah Shelby 01 January 2011 (has links)
Understanding gene flow, diversity, and dispersal patterns is important for predicting effects of natural events and anthropogenic activities on dolphin populations. With the very recent exceptions of false killer whales (Pseudorca crassidens), spinner dolphins (Stenella longirostris), and common bottlenose dolphins (Tursiops truncatus), Hawaiian odontocete species are managed as single stocks within the U.S. Hawaiian Exclusive Economic Zone. These exceptions are a result of recent studies that have indicated that some species have populations that show fidelity to individual islands or groups of islands, resulting in genetic differentiation, often with management implications. The first part of my study (following the introductory chapter) focused on population structure of pantropical spotted dolphins (Stenella attenuata) near the Hawaiian Islands. Because of the level of human interaction, pantropical spotted dolphin populations need to be defined accurately to be managed in a way that will avoid local population losses, especially given that the commercial and recreational troll fisheries near the islands "fish on dolphins" to catch tuna. I analyzed genetic samples for mtDNA and microsatellite loci from four island regions: Hawai'i, the 4-islands area, O'ahu, and Kaua'i/Ni'ihau. My results support genetic differentiation among the regions of Hawai'i, the 4-islands area, and O'ahu and suggest that pantropical spotted dolphins near Kaua'i/Ni'ihau are likely transient and in very low numbers. There was no strong evidence to support sex-biased dispersal or group fidelity. Possibly, differentiation is mediated by behavior adapted to differing habitat types. From a management perspective, spinner and bottlenose dolphin populations near the Hawaiian Islands have been split into separate stocks for management based on levels of genetic differentiation similar to those found for pantropical spotted dolphins. These precedents suggest that comparable action should be taken to split pantropical spotted dolphin stocks near the Hawaiian Islands. Most population studies rely heavily upon fixation indicies like FST to determine whether populations are genetically differentiated. When FST values are low but significantly different from zero, it can be difficult to interpret the biological significance of these values. As part of my study, I suggest that one way to evaluate whether small FST values indicate significant differentiation is to compare FST values with other populations considered to be separate based on factors such as extreme distance or morphological differences. I examined pantropical spotted dolphins from the coastal and offshore Eastern Tropical Pacificm (ETP), Hawaiian Islands, and China/Taiwan to examine the utility of comparing FST values across separate populations. Among Hawaiian Island regions, FST values are significantly different from zero but small. The comparison of these FST values with more distant populations in the ETP and China/Taiwan indicated that differences among Hawaiian Island regions were similar in magnitude to those found between the offshore and coastal ETP sub-species, but smaller than between the Hawaiian Island regions and the other regions examined. This suggests a level of reproductive isolation among the Hawaiian Islands regions that is comparable to that of offshore and coastal ETP populations, and supports the value of fixation index comparisons in evaluating differentiation among putative populations. My results suggest that assigning specific numerical baseline FST values may not always be biologically meaningful but that determining whether related populations with geographic or other separation show a preponderance of similar, lower, or higher fixation index values can help evaluate whether genetic differences among sympatric or parapatric groups warrants designating them as separate populations for management. Lastly, I explore whether the fast evolving mtDNA control region may be more suited to phylogenetic comparisons among the Stenella than slower evolving gene regions and whether the small number of haplotypes generally used in phylogenetic analyses is adequate for defining relationships among dolphins. Usually, slow evolving regions, such as gene regions, are used in phylogenetic analyses because species and genera have been isolated long enough for variation to have accumulated in such regions but not so long that many reversals (i.e. a mutational change in sequence that later changes back to the original sequence) have occured. The mtDNA control region is typically used for population genetic comparisons rather than phylogenetic comparisons because it is considered to be a fast evolving region. Historically, dolphin phylogeny has been examined using gene regions, which have resulted in ambiguous and unexpected relationships. However, the lack of variation in the mtDNA control region for pantropical spotted dolphin populations and the fact that recent studies have found that the mtDNA control region in cetaceans evolves at about one quarter the rate of other mammals, raises the question as to whether this region would be better suited to phylogenetic studies for the Stenella (and potentially other dolphin species). In comparing 346 haplotypes from five species of Stenella world-wide, I found that the mtDNA control region is probably not a good region to use for phylogenetic analyses, and that even faster evolving regions might perform better. The differences in the mtDNA control region were not sufficient to distinguish clear relationships among the Stenella. I also found that when subsets of haplotypes chosen at random were compared, the results differed among comparisons, suggesting that there is value in using more than the usual one or two haplotypes when making phylogentic comparisons. Given the recent increases in sequence availability (e.g. GenBank) and computing power, researchers should strongly consider using many haplotypes from a variety of populations in their phylogenetic comparisons.
17

Studying the effects of a 'captive breeding program' on additive genetic variance using Drosophila melanogaster relocation to a novel environment /

McCurry, Elizabeth Mae. January 2009 (has links)
Thesis (M.S.)--State University of New York at Binghamton, Department of Biological Studies, 2009. / Includes bibliographical references.
18

The evolutionary and demographic consequences of gene flow in a threespine stickleback population /

Moore, Jean-Sébastien. January 2007 (has links)
No description available.
19

The evolutionary and demographic consequences of gene flow in a threespine stickleback population /

Moore, Jean-Sébastien. January 2007 (has links)
I here explore the dual roles of gene flow in determining evolutionary and demographic processes in the Misty Lake threespine stickleback (Gasterosteus aculeatus L.). In the Misty watershed, the lake fish have streamlined bodies and numerous gill rakers whereas the inlet stream fish have deeper bodies and reduced number of gill rakers, differences that are adaptive for lake and stream environments respectively. The outlet stream population, however, is morphologically intermediate between the lake and inlet populations as a result of high gene flow from the lake preventing adaptation to the stream environment. First, I quantify the constraining effect of gene flow on adaptive divergence in the Misty outlet using two complementary approaches. By comparing phenotypic values and environmental differences between the three habitats (i.e. lake, inlet and outlet), I estimate that the constraint imposed by gene flow on phenotypic divergence is in the order of 80%, i.e. the outlet population only achieves 20% of the phenotypic divergence expected in the absence of gene flow. Parameterization of a quantitative genetic model confirms this value is possible given a biologically realistic range of parameter values. Second, I demonstrate that this constraint imposed by gene flow on adaptation likely contributes to an observed reduction in abundances along the outlet stream. I do so using a transplant experiment and a three-year selection experiment. Quantification of the amount of dispersal suggests that the negative influence of gene flow offsets the positive demographic influence of the immigration of individuals. In summary, gene flow has profound consequences for both evolutionary and demographic processes taking place in the Misty system.
20

Changes in genetic architecture in a 'captive breeding program" of Drosophila melanogaster

Davis, Eloiza Marie. January 2009 (has links)
Thesis (M.S.)--State University of New York at Binghamton, Department of Biological Sciences, 2009. / Includes bibliographical references.

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