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ECOLOGICAL MORPHOLOGY OF BREEDING BIRDS IN OLD WORLD AND NEW WORLD PEATLANDS (MINNESOTA, FINLAND)Unknown Date (has links)
Morphological convergence is defined here as evolution toward similar dimensions of traits in unrelated animals that live in the same or similar environments. Because a genus is a taxonomic unit in which differences among congeners represent directional changes in morphology from a common ancestor, I look for evidence of morphological convergence by comparing sets of congeneric species of birds that breed in peatland habitats of northern Minnesota and eastern Finland. / I identified similar peatland habitats in Finland and in Minnesota in a space determined by discriminant function analysis. Shrub areas and coniferous forest areas were similar to shrub areas and coniferous forest areas, respectively, regardless of continent. Therefore, I identified four genera in Minnesota, Zonotrichia, Spizella, Geothlypis, and Dendroica, and one in Finland, Emberiza, with species in shrub and in coniferous forest peatlands and compared their morphology. / The species in shrub vegetation were smaller, had relatively longer pelves and legs, and had wider and shallower sterna compared with their congeners in coniferous forest. With the exception of Emberiza, the length of the bill and the length of the wings were also relatively longer for the shrub-dwelling peatland species. Warblers breeding in shrub peatlands had relatively deeper and wider bills, but sparrows had relatively shallower and narrower bills compared with their congeners in coniferous forests. / These results indicate significant (p = .03) directional patterns among taxonomically distantly-related genera for morphology associated with movement through the vegetation. Morphology associated with feeding, however, shows trends at a familial level that probably reflect differences in diet and behavior between sparrows and warblers. The consistency of the patterns emphasizes (1) the relationship between morphology and habitat structure or behavior, and (2) the likelihood of a common underlying mechanism for these patterns. / Source: Dissertation Abstracts International, Volume: 44-02, Section: B, page: 0401. / Thesis (Ph.D.)--The Florida State University, 1983.
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How do leaf functional traits vary across ecological scales?Messier, Julie January 2009 (has links)
No description available.
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The effect of harvesting on size structured predatory and competitive interactions between rainbow trout («Oncorhynchus mykiss») and northern pikeminnow («Ptychocheilus oregonensis»)O'Brien, David Sean January 2009 (has links)
No description available.
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Geographic and habitat fidelity in the short-eared owl (Asio flammeus)Keyes, Kristen January 2011 (has links)
No description available.
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Predator-prey ecological and evolutionary dynamics: The cost of a counter-defense drives the evolutionary outcomeGregg, Tamara January 2011 (has links)
No description available.
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Forecasting the impacts of climate change with non-stationary models of regional population densitySamson, Jason January 2011 (has links)
No description available.
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Assessing the relationship between propagule pressure and probability of establishment for the aquatic invader «Bythotrephes longimanus» using two complementary approachesGertzen, Erin January 2010 (has links)
No description available.
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Invasion dynamics of exotic and native common reed in fresh water wetlandsDenis, Jean-François January 2011 (has links)
No description available.
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Using case-based reasoning to learn about ecological engineeringLanphere, Tania Ruth January 2010 (has links)
No description available.
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Community-level effects of nonindigenous aquatic ecosystem engineersWard, Jessica MacKay January 2010 (has links)
No description available.
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