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Can Preference for Oviposition Sites Initiate Reproductive Isolation in Callosobruchus maculatus?

Theory has identified a variety of evolutionary processes that may lead to speciation. Our study includes selection experiments using different host plants and test key predictions concerning models of speciation based on host plant choice, such as the evolution of host use (preference and performan...

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Detalles Bibliográficos
Autores principales: Rova, Emma, Björklund, Mats
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031505/
https://www.ncbi.nlm.nih.gov/pubmed/21297947
http://dx.doi.org/10.1371/journal.pone.0014628
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author Rova, Emma
Björklund, Mats
author_facet Rova, Emma
Björklund, Mats
author_sort Rova, Emma
collection PubMed
description Theory has identified a variety of evolutionary processes that may lead to speciation. Our study includes selection experiments using different host plants and test key predictions concerning models of speciation based on host plant choice, such as the evolution of host use (preference and performance) and assortative mating. This study shows that after only ten generations of selection on different resources/hosts in allopatry, strains of the seed beetle Callosobruchus maculatus develop new resource preferences and show resource-dependent assortative mating when given the possibility to choose mates and resources during secondary contact. The resulting reduced gene flow between the different strains remained for two generations after contact before being overrun by disassortative mating. We show that reduced gene flow can evolve in a population due to a link between host preference and assortative mating, although this result was not found in all lines. However, consistent with models of speciation, assortative mating alone is not sufficient to maintain reproductive isolation when individuals disperse freely between hosts. We conclude that the evolution of reproductive isolation in this system cannot proceed without selection against hybrids. Other possible factors facilitating the evolution of isolation would be longer periods of allopatry, the build up of local adaptation or reduced migration upon secondary contact.
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spelling pubmed-30315052011-02-04 Can Preference for Oviposition Sites Initiate Reproductive Isolation in Callosobruchus maculatus? Rova, Emma Björklund, Mats PLoS One Research Article Theory has identified a variety of evolutionary processes that may lead to speciation. Our study includes selection experiments using different host plants and test key predictions concerning models of speciation based on host plant choice, such as the evolution of host use (preference and performance) and assortative mating. This study shows that after only ten generations of selection on different resources/hosts in allopatry, strains of the seed beetle Callosobruchus maculatus develop new resource preferences and show resource-dependent assortative mating when given the possibility to choose mates and resources during secondary contact. The resulting reduced gene flow between the different strains remained for two generations after contact before being overrun by disassortative mating. We show that reduced gene flow can evolve in a population due to a link between host preference and assortative mating, although this result was not found in all lines. However, consistent with models of speciation, assortative mating alone is not sufficient to maintain reproductive isolation when individuals disperse freely between hosts. We conclude that the evolution of reproductive isolation in this system cannot proceed without selection against hybrids. Other possible factors facilitating the evolution of isolation would be longer periods of allopatry, the build up of local adaptation or reduced migration upon secondary contact. Public Library of Science 2011-01-31 /pmc/articles/PMC3031505/ /pubmed/21297947 http://dx.doi.org/10.1371/journal.pone.0014628 Text en Rova, Björklund. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rova, Emma
Björklund, Mats
Can Preference for Oviposition Sites Initiate Reproductive Isolation in Callosobruchus maculatus?
title Can Preference for Oviposition Sites Initiate Reproductive Isolation in Callosobruchus maculatus?
title_full Can Preference for Oviposition Sites Initiate Reproductive Isolation in Callosobruchus maculatus?
title_fullStr Can Preference for Oviposition Sites Initiate Reproductive Isolation in Callosobruchus maculatus?
title_full_unstemmed Can Preference for Oviposition Sites Initiate Reproductive Isolation in Callosobruchus maculatus?
title_short Can Preference for Oviposition Sites Initiate Reproductive Isolation in Callosobruchus maculatus?
title_sort can preference for oviposition sites initiate reproductive isolation in callosobruchus maculatus?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031505/
https://www.ncbi.nlm.nih.gov/pubmed/21297947
http://dx.doi.org/10.1371/journal.pone.0014628
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