Ecological speciation in an island snail: evidence for the parallel evolution of a novel ecotype and maintenance by ecologically dependent postzygotic isolation
Speciation is the process by which reproductive isolation evolves between populations. Two general models of speciation have been proposed: ecological speciation, where reproductive barriers evolve due to ecologically based divergent selection, and mutation‐order speciation, where populations fix di...
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Veröffentlicht in: | Molecular ecology 2013-05, Vol.22 (10), p.2726-2741 |
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description | Speciation is the process by which reproductive isolation evolves between populations. Two general models of speciation have been proposed: ecological speciation, where reproductive barriers evolve due to ecologically based divergent selection, and mutation‐order speciation, where populations fix different mutations as they adapt to similar selection pressures. I evaluate these alternative models and determine the progress of speciation in a diverse group of land snails, genus Rhagada, inhabiting Rosemary Island. A recently derived keeled‐flat morphotype occupies two isolated rocky hills, while globose‐shelled snails inhabit the surrounding plains. The study of one hill reveals that they are separated by a narrow hybrid zone. As predicted by ecological speciation theory, there are local and landscape level associations between shell shape and habitat, and the morphological transition coincides with a narrow ecotone between the two distinct environments. Microsatellite DNA revealed a cline of hybrid index scores much wider than the morphological cline, further supporting the ecological maintenance of the morphotypes. The hybrid zone does not run through an area of low population density, as is expected for mutation‐order hybrid zones, and there is a unimodal distribution of phenotypes at the centre, suggesting that there is little or no prezygotic isolation. Instead, these data suggest that the ecotypes are maintained by ecologically dependent postzygotic isolation (i.e. ecological selection against hybrids). Mitochondrial and Microsatellite DNA indicate that the keeled‐flat form evolved recently, and without major historical disruptions to gene flow. The data also suggest that the two keeled‐flat populations, inhabiting similar rocky hills, have evolved in parallel. These snails provide a complex example of ecological speciation in its early stages. |
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Two general models of speciation have been proposed: ecological speciation, where reproductive barriers evolve due to ecologically based divergent selection, and mutation‐order speciation, where populations fix different mutations as they adapt to similar selection pressures. I evaluate these alternative models and determine the progress of speciation in a diverse group of land snails, genus Rhagada, inhabiting Rosemary Island. A recently derived keeled‐flat morphotype occupies two isolated rocky hills, while globose‐shelled snails inhabit the surrounding plains. The study of one hill reveals that they are separated by a narrow hybrid zone. As predicted by ecological speciation theory, there are local and landscape level associations between shell shape and habitat, and the morphological transition coincides with a narrow ecotone between the two distinct environments. Microsatellite DNA revealed a cline of hybrid index scores much wider than the morphological cline, further supporting the ecological maintenance of the morphotypes. The hybrid zone does not run through an area of low population density, as is expected for mutation‐order hybrid zones, and there is a unimodal distribution of phenotypes at the centre, suggesting that there is little or no prezygotic isolation. Instead, these data suggest that the ecotypes are maintained by ecologically dependent postzygotic isolation (i.e. ecological selection against hybrids). Mitochondrial and Microsatellite DNA indicate that the keeled‐flat form evolved recently, and without major historical disruptions to gene flow. The data also suggest that the two keeled‐flat populations, inhabiting similar rocky hills, have evolved in parallel. These snails provide a complex example of ecological speciation in its early stages.</description><identifier>ISSN: 0962-1083</identifier><identifier>EISSN: 1365-294X</identifier><identifier>DOI: 10.1111/mec.12287</identifier><identifier>PMID: 23506623</identifier><language>eng</language><publisher>Oxford: Blackwell Publishing Ltd</publisher><subject>Adaptation, Biological - genetics ; Animal Distribution ; Animal populations ; Animal Shells - anatomy & histology ; Animals ; Biological and medical sciences ; Biological Evolution ; DNA, Mitochondrial - genetics ; Evolutionary biology ; Fundamental and applied biological sciences. Psychology ; Genetic Speciation ; Genetics of eukaryotes. Biological and molecular evolution ; Geography ; Habitats ; hybrid zone patchwork ; Hybridization, Genetic ; Invertebrates ; Islands ; land snail ; Microsatellite Repeats - genetics ; Models, Genetic ; Mollusca ; Mollusks ; Morphology ; mosaic landscape ; parapatric divergence ; Population Density ; Population genetics, reproduction patterns ; Reproductive Isolation ; Rosmarinus ; Selection, Genetic ; shell shape ; Snails - anatomy & histology ; Snails - genetics ; unimodal hybrid zone ; Western Australia</subject><ispartof>Molecular ecology, 2013-05, Vol.22 (10), p.2726-2741</ispartof><rights>2013 Blackwell Publishing Ltd</rights><rights>2014 INIST-CNRS</rights><rights>2013 Blackwell Publishing Ltd.</rights><rights>Copyright © 2013 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5207-df9afa4bc0e4020c25ba498abbc1015ee51cbc3d2be3893b14e65fb4a58f89033</citedby><cites>FETCH-LOGICAL-c5207-df9afa4bc0e4020c25ba498abbc1015ee51cbc3d2be3893b14e65fb4a58f89033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fmec.12287$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fmec.12287$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27395530$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23506623$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stankowski, Sean</creatorcontrib><title>Ecological speciation in an island snail: evidence for the parallel evolution of a novel ecotype and maintenance by ecologically dependent postzygotic isolation</title><title>Molecular ecology</title><addtitle>Mol Ecol</addtitle><description>Speciation is the process by which reproductive isolation evolves between populations. Two general models of speciation have been proposed: ecological speciation, where reproductive barriers evolve due to ecologically based divergent selection, and mutation‐order speciation, where populations fix different mutations as they adapt to similar selection pressures. I evaluate these alternative models and determine the progress of speciation in a diverse group of land snails, genus Rhagada, inhabiting Rosemary Island. A recently derived keeled‐flat morphotype occupies two isolated rocky hills, while globose‐shelled snails inhabit the surrounding plains. The study of one hill reveals that they are separated by a narrow hybrid zone. As predicted by ecological speciation theory, there are local and landscape level associations between shell shape and habitat, and the morphological transition coincides with a narrow ecotone between the two distinct environments. Microsatellite DNA revealed a cline of hybrid index scores much wider than the morphological cline, further supporting the ecological maintenance of the morphotypes. The hybrid zone does not run through an area of low population density, as is expected for mutation‐order hybrid zones, and there is a unimodal distribution of phenotypes at the centre, suggesting that there is little or no prezygotic isolation. Instead, these data suggest that the ecotypes are maintained by ecologically dependent postzygotic isolation (i.e. ecological selection against hybrids). Mitochondrial and Microsatellite DNA indicate that the keeled‐flat form evolved recently, and without major historical disruptions to gene flow. The data also suggest that the two keeled‐flat populations, inhabiting similar rocky hills, have evolved in parallel. These snails provide a complex example of ecological speciation in its early stages.</description><subject>Adaptation, Biological - genetics</subject><subject>Animal Distribution</subject><subject>Animal populations</subject><subject>Animal Shells - anatomy & histology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biological Evolution</subject><subject>DNA, Mitochondrial - genetics</subject><subject>Evolutionary biology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic Speciation</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Geography</subject><subject>Habitats</subject><subject>hybrid zone patchwork</subject><subject>Hybridization, Genetic</subject><subject>Invertebrates</subject><subject>Islands</subject><subject>land snail</subject><subject>Microsatellite Repeats - genetics</subject><subject>Models, Genetic</subject><subject>Mollusca</subject><subject>Mollusks</subject><subject>Morphology</subject><subject>mosaic landscape</subject><subject>parapatric divergence</subject><subject>Population Density</subject><subject>Population genetics, reproduction patterns</subject><subject>Reproductive Isolation</subject><subject>Rosmarinus</subject><subject>Selection, Genetic</subject><subject>shell shape</subject><subject>Snails - anatomy & histology</subject><subject>Snails - genetics</subject><subject>unimodal hybrid zone</subject><subject>Western Australia</subject><issn>0962-1083</issn><issn>1365-294X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkd1qFTEUhYMo9li98AUkIIJeTJvf-fFODscqtEpBrXchk9lTUzOTMZmpjk_jo5o557SCIJiLBLK_vVayF0KPKTmiaR13YI4oY2VxB60oz2XGKvH5LlqRKmcZJSU_QA9ivCKEciblfXTAuCR5zvgK_doY7_ylNdrhOICxerS-x7bHOu3R6b7BsdfWvcRwbRvoDeDWBzx-ATzooJ0DlyreTds-32KNe3-9XBo_zgPgRaHTth-h10t3PS-lvaebcQMD9El4xIOP48_50o_WJGvvtk95iO612kV4tD8P0cfXmw_rN9np-5O361enmZGMFFnTVrrVojYEBGHEMFlrUZW6rg0lVAJIamrDG1YDLyteUwG5bGuhZdmWFeH8ED3f6Q7Bf5sgjqqz0YBLEwA_RUW5ZKxigpH_QEVOacnZovr0L_TKT6FPH0kULxmnZOv9YkeZ4GMM0Koh2E6HWVGiloRVSlhtE07sk73iVHfQ3JI3kSbg2R7QMU24DWnqNv7hCl5JyZdfHO-479bB_G9HdbZZ31hnuw4bR_hx26HDV5UXvJDq4t2JKs8uzj-JtVDn_De8ws54</recordid><startdate>201305</startdate><enddate>201305</enddate><creator>Stankowski, Sean</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201305</creationdate><title>Ecological speciation in an island snail: evidence for the parallel evolution of a novel ecotype and maintenance by ecologically dependent postzygotic isolation</title><author>Stankowski, Sean</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5207-df9afa4bc0e4020c25ba498abbc1015ee51cbc3d2be3893b14e65fb4a58f89033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adaptation, Biological - genetics</topic><topic>Animal Distribution</topic><topic>Animal populations</topic><topic>Animal Shells - anatomy & histology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biological Evolution</topic><topic>DNA, Mitochondrial - genetics</topic><topic>Evolutionary biology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic Speciation</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Geography</topic><topic>Habitats</topic><topic>hybrid zone patchwork</topic><topic>Hybridization, Genetic</topic><topic>Invertebrates</topic><topic>Islands</topic><topic>land snail</topic><topic>Microsatellite Repeats - genetics</topic><topic>Models, Genetic</topic><topic>Mollusca</topic><topic>Mollusks</topic><topic>Morphology</topic><topic>mosaic landscape</topic><topic>parapatric divergence</topic><topic>Population Density</topic><topic>Population genetics, reproduction patterns</topic><topic>Reproductive Isolation</topic><topic>Rosmarinus</topic><topic>Selection, Genetic</topic><topic>shell shape</topic><topic>Snails - anatomy & histology</topic><topic>Snails - genetics</topic><topic>unimodal hybrid zone</topic><topic>Western Australia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stankowski, Sean</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stankowski, Sean</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ecological speciation in an island snail: evidence for the parallel evolution of a novel ecotype and maintenance by ecologically dependent postzygotic isolation</atitle><jtitle>Molecular ecology</jtitle><addtitle>Mol Ecol</addtitle><date>2013-05</date><risdate>2013</risdate><volume>22</volume><issue>10</issue><spage>2726</spage><epage>2741</epage><pages>2726-2741</pages><issn>0962-1083</issn><eissn>1365-294X</eissn><abstract>Speciation is the process by which reproductive isolation evolves between populations. Two general models of speciation have been proposed: ecological speciation, where reproductive barriers evolve due to ecologically based divergent selection, and mutation‐order speciation, where populations fix different mutations as they adapt to similar selection pressures. I evaluate these alternative models and determine the progress of speciation in a diverse group of land snails, genus Rhagada, inhabiting Rosemary Island. A recently derived keeled‐flat morphotype occupies two isolated rocky hills, while globose‐shelled snails inhabit the surrounding plains. The study of one hill reveals that they are separated by a narrow hybrid zone. As predicted by ecological speciation theory, there are local and landscape level associations between shell shape and habitat, and the morphological transition coincides with a narrow ecotone between the two distinct environments. Microsatellite DNA revealed a cline of hybrid index scores much wider than the morphological cline, further supporting the ecological maintenance of the morphotypes. The hybrid zone does not run through an area of low population density, as is expected for mutation‐order hybrid zones, and there is a unimodal distribution of phenotypes at the centre, suggesting that there is little or no prezygotic isolation. Instead, these data suggest that the ecotypes are maintained by ecologically dependent postzygotic isolation (i.e. ecological selection against hybrids). Mitochondrial and Microsatellite DNA indicate that the keeled‐flat form evolved recently, and without major historical disruptions to gene flow. The data also suggest that the two keeled‐flat populations, inhabiting similar rocky hills, have evolved in parallel. These snails provide a complex example of ecological speciation in its early stages.</abstract><cop>Oxford</cop><pub>Blackwell Publishing Ltd</pub><pmid>23506623</pmid><doi>10.1111/mec.12287</doi><tpages>16</tpages></addata></record> |
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subjects | Adaptation, Biological - genetics Animal Distribution Animal populations Animal Shells - anatomy & histology Animals Biological and medical sciences Biological Evolution DNA, Mitochondrial - genetics Evolutionary biology Fundamental and applied biological sciences. Psychology Genetic Speciation Genetics of eukaryotes. Biological and molecular evolution Geography Habitats hybrid zone patchwork Hybridization, Genetic Invertebrates Islands land snail Microsatellite Repeats - genetics Models, Genetic Mollusca Mollusks Morphology mosaic landscape parapatric divergence Population Density Population genetics, reproduction patterns Reproductive Isolation Rosmarinus Selection, Genetic shell shape Snails - anatomy & histology Snails - genetics unimodal hybrid zone Western Australia |
title | Ecological speciation in an island snail: evidence for the parallel evolution of a novel ecotype and maintenance by ecologically dependent postzygotic isolation |
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