1997
DOI: 10.2307/2410956
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Genetic Models of Adaptation and Gene Flow in Peripheral Populations

Abstract: We investigate the interplay between gene flow and adaptation in peripheral populations of a widespread species. Models are developed for the evolution of a quantitative trait under clinally varying selection in a species whose density decreases from the center of the range to its periphery. Two major results emerge. First, gene flow from populations at the range center can be a strong force that inhibits peripheral populations from evolving to their local ecological optima. As a result, peripheral populations… Show more

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Cited by 397 publications
(434 citation statements)
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“…Island populations of tortoises (Caccone et al 2002), beetles (Finston & Peck 1995) and lizards (Wright 1983) in the Galápagos, and Drosophila (Desalle 1995), spiders (Hormiga et al 2003) and crickets (Shaw 2002) in Hawaii tend to be genetically more closely related if they occur on neighbouring islands. The abundant evidence from nature has led to the assumption of distance-limited dispersal in models of island biogeography (MacArthur & Wilson 1967), geographical clines (Endler 1977;Kirkpatrick & Barton 1997), metapopulation dynamics (Hanski & Gilpin 1997) and speciation (Mayr 1942;Garcia-Ramos & Kirkpatrick 1997).…”
Section: Introductionmentioning
confidence: 99%
“…Island populations of tortoises (Caccone et al 2002), beetles (Finston & Peck 1995) and lizards (Wright 1983) in the Galápagos, and Drosophila (Desalle 1995), spiders (Hormiga et al 2003) and crickets (Shaw 2002) in Hawaii tend to be genetically more closely related if they occur on neighbouring islands. The abundant evidence from nature has led to the assumption of distance-limited dispersal in models of island biogeography (MacArthur & Wilson 1967), geographical clines (Endler 1977;Kirkpatrick & Barton 1997), metapopulation dynamics (Hanski & Gilpin 1997) and speciation (Mayr 1942;Garcia-Ramos & Kirkpatrick 1997).…”
Section: Introductionmentioning
confidence: 99%
“…The evolution and ecology of peripheral populations are driven by various genetic and demographic processes. For example, adaptation to local conditions depends greatly on the level of gene flow from the core population (García-Ramos and Kirkpatrick 1997;Lenormand 2002). Although it is generally acknowledged that low gene flow facilitates rapid divergence at a range margin (Felsenstein 1976;Slatkin 1985;García-Ramos and Kirkpatrick 1997), gene flow can play ambiguous roles in adaptation to local conditions, depending on additional factors.…”
Section: Introductionmentioning
confidence: 99%
“…For example, adaptation to local conditions depends greatly on the level of gene flow from the core population (García-Ramos and Kirkpatrick 1997;Lenormand 2002). Although it is generally acknowledged that low gene flow facilitates rapid divergence at a range margin (Felsenstein 1976;Slatkin 1985;García-Ramos and Kirkpatrick 1997), gene flow can play ambiguous roles in adaptation to local conditions, depending on additional factors. If a peripheral population is isolated from the core population, it may never adapt to local conditions because of genetic drift and low mutational input that causes deficiency of beneficial mutations (Kawecki 2000;Bridle and Vines 2006).…”
Section: Introductionmentioning
confidence: 99%
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“…Additionally, the more homogenous environments of oceanic fishes compared to estuarine fishes may result in weaker environmental selection pressures, also making spatial adaptations less likely. If oceanic species tend to lack genetic structure, they may be limited in their ability to respond to climate change, since populations may not be able to respond differently across their range (Garcia-Ramos & Kirkpatrick 1997, Lenormand 2002.…”
Section: Introductionmentioning
confidence: 99%