The Amarillo (Girardinichthys multiradiatus) a fish model to study geographic variation in mate recognition systems
Identifieur interne : 001591 ( Istex/Corpus ); précédent : 001590; suivant : 001592The Amarillo (Girardinichthys multiradiatus) a fish model to study geographic variation in mate recognition systems
Auteurs : C. Gonzalez-Zuarth ; E. Avila ; C. Macías GarciaSource :
- Journal of Fish Biology [ 0022-1112 ] ; 2003-12.
Abstract
The existence of a species‐specific mate recognition system (MRS) enables a fluid interchange of genes within species, while promoting the evolution of barriers to hybridization across sibling species. This is because MRS's can diverge in allopatry as a consequence of random events such as drift, or because different ecological conditions impose different optima on sexually‐selected characters such as may be part of the MRS’s. As freshwater habitats are frequently fragmented and re‐merged following long‐term climatic changes and river piracy across catchments, there is ample scope for fish populations’ MRS's to diverge in allopatry to the point of generating pre‐mating barriers. Based on former records of population differences in sexually‐dimorphic traits in the Amarillo fish (Girardinichthys multiradiatus), we investigated 1) whether courtship by males is quantifiably different between populations, and 2) whether these differences are due to difference in the way females respond to specific elements of the courtship sequence (thus prompting males to court in a population‐specific style). Using five populations representing the whole of the Amarillo's geographic range, we found that, when confronted to homogametic females, males exhibited substantial and significant differences in the tendency to perform particular courtship patterns, in spite of males form all populations having equal repertoires. We also found that heterogametic courtship neither resembled that of the populations of origin of the male, nor of the female. We infer that the interpretation of the courtship signals is diverging across Amarillo populations, in a manner akin to the evolution of languages in bird songs.
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DOI: 10.1111/j.1095-8649.2003.216be.x
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This is because MRS's can diverge in allopatry as a consequence of random events such as drift, or because different ecological conditions impose different optima on sexually‐selected characters such as may be part of the MRS’s. As freshwater habitats are frequently fragmented and re‐merged following long‐term climatic changes and river piracy across catchments, there is ample scope for fish populations’ MRS's to diverge in allopatry to the point of generating pre‐mating barriers. Based on former records of population differences in sexually‐dimorphic traits in the Amarillo fish (Girardinichthys multiradiatus), we investigated 1) whether courtship by males is quantifiably different between populations, and 2) whether these differences are due to difference in the way females respond to specific elements of the courtship sequence (thus prompting males to court in a population‐specific style). Using five populations representing the whole of the Amarillo's geographic range, we found that, when confronted to homogametic females, males exhibited substantial and significant differences in the tendency to perform particular courtship patterns, in spite of males form all populations having equal repertoires. We also found that heterogametic courtship neither resembled that of the populations of origin of the male, nor of the female. We infer that the interpretation of the courtship signals is diverging across Amarillo populations, in a manner akin to the evolution of languages in bird songs.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>C. Gonzalez‐Zuarth</name><affiliations><json:string>(Instituto de Ecologia, UNAM, A.P. 70‐275. Mexico, D.F. C.P 04510, Mexico ).</json:string></affiliations></json:item><json:item><name>E. Avila</name><affiliations><json:string>(Instituto de Ecologia, UNAM, A.P. 70‐275. Mexico, D.F. 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As freshwater habitats are frequently fragmented and re‐merged following long‐term climatic changes and river piracy across catchments, there is ample scope for fish populations’ MRS's to diverge in allopatry to the point of generating pre‐mating barriers. Based on former records of population differences in sexually‐dimorphic traits in the Amarillo fish (Girardinichthys multiradiatus), we investigated 1) whether courtship by males is quantifiably different between populations, and 2) whether these differences are due to difference in the way females respond to specific elements of the courtship sequence (thus prompting males to court in a population‐specific style). Using five populations representing the whole of the Amarillo's geographic range, we found that, when confronted to homogametic females, males exhibited substantial and significant differences in the tendency to perform particular courtship patterns, in spite of males form all populations having equal repertoires. We also found that heterogametic courtship neither resembled that of the populations of origin of the male, nor of the female. 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Using five populations representing the whole of the Amarillo's geographic range, we found that, when confronted to homogametic females, males exhibited substantial and significant differences in the tendency to perform particular courtship patterns, in spite of males form all populations having equal repertoires. We also found that heterogametic courtship neither resembled that of the populations of origin of the male, nor of the female. 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Based on former records of population differences in sexually‐dimorphic traits in the Amarillo fish (<i>Girardinichthys multiradiatus</i>), we investigated 1) whether courtship by males is quantifiably different between populations, and 2) whether these differences are due to difference in the way females respond to specific elements of the courtship sequence (thus prompting males to court in a population‐specific style). Using five populations representing the whole of the Amarillo's geographic range, we found that, when confronted to homogametic females, males exhibited substantial and significant differences in the tendency to perform particular courtship patterns, in spite of males form all populations having equal repertoires. We also found that heterogametic courtship neither resembled that of the populations of origin of the male, nor of the female. 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This is because MRS's can diverge in allopatry as a consequence of random events such as drift, or because different ecological conditions impose different optima on sexually‐selected characters such as may be part of the MRS’s. As freshwater habitats are frequently fragmented and re‐merged following long‐term climatic changes and river piracy across catchments, there is ample scope for fish populations’ MRS's to diverge in allopatry to the point of generating pre‐mating barriers. Based on former records of population differences in sexually‐dimorphic traits in the Amarillo fish (Girardinichthys multiradiatus), we investigated 1) whether courtship by males is quantifiably different between populations, and 2) whether these differences are due to difference in the way females respond to specific elements of the courtship sequence (thus prompting males to court in a population‐specific style). Using five populations representing the whole of the Amarillo's geographic range, we found that, when confronted to homogametic females, males exhibited substantial and significant differences in the tendency to perform particular courtship patterns, in spite of males form all populations having equal repertoires. We also found that heterogametic courtship neither resembled that of the populations of origin of the male, nor of the female. We infer that the interpretation of the courtship signals is diverging across Amarillo populations, in a manner akin to the evolution of languages in bird songs.</abstract><relatedItem type="host"><titleInfo><title>Journal of Fish Biology</title></titleInfo><genre type="journal">journal</genre><identifier type="ISSN">0022-1112</identifier><identifier type="eISSN">1095-8649</identifier><identifier type="DOI">10.1111/(ISSN)1095-8649</identifier><identifier type="PublisherID">JFB</identifier><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>63</number></detail><detail type="supplement"><caption>Suppl. no.</caption><number>s1</number></detail><extent unit="pages"><start>251</start><end>252</end><total>2</total></extent></part></relatedItem><identifier type="istex">FEE65546B6DF46B271959AD625E054A29A1A3A54</identifier><identifier type="DOI">10.1111/j.1095-8649.2003.216be.x</identifier><identifier type="ArticleID">JFB216BE</identifier><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Science Ltd/Inc</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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