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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...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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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. |
format | Text |
id | pubmed-3031505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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