Physiological adaptation along environmental gradients and replicated hybrid zone structure in swordtails (Teleostei: Xiphophorus)
Local adaptation is often invoked to explain hybrid zone structure, but empirical evidence of this is generally rare. Hybrid zones between two poeciliid fishes, Xiphophorus birchmanni and X. malinche, occur in multiple tributaries with independent replication of upstream‐to‐downstream gradients in m...
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description | Local adaptation is often invoked to explain hybrid zone structure, but empirical evidence of this is generally rare. Hybrid zones between two poeciliid fishes, Xiphophorus birchmanni and X. malinche, occur in multiple tributaries with independent replication of upstream‐to‐downstream gradients in morphology and allele frequencies. Ecological niche modelling revealed that temperature is a central predictive factor in the spatial distribution of pure parental species and their hybrids and explains spatial and temporal variation in the frequency of neutral genetic markers in hybrid populations. Among populations of parentals and hybrids, both thermal tolerance and heat‐shock protein expression vary strongly, indicating that spatial and temporal structure is likely driven by adaptation to local thermal environments. Therefore, hybrid zone structure is strongly influenced by interspecific differences in physiological mechanisms for coping with the thermal environment. |
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Hybrid zones between two poeciliid fishes, Xiphophorus birchmanni and X. malinche, occur in multiple tributaries with independent replication of upstream‐to‐downstream gradients in morphology and allele frequencies. Ecological niche modelling revealed that temperature is a central predictive factor in the spatial distribution of pure parental species and their hybrids and explains spatial and temporal variation in the frequency of neutral genetic markers in hybrid populations. Among populations of parentals and hybrids, both thermal tolerance and heat‐shock protein expression vary strongly, indicating that spatial and temporal structure is likely driven by adaptation to local thermal environments. Therefore, hybrid zone structure is strongly influenced by interspecific differences in physiological mechanisms for coping with the thermal environment.</description><identifier>ISSN: 1010-061X</identifier><identifier>EISSN: 1420-9101</identifier><identifier>DOI: 10.1111/j.1420-9101.2012.02562.x</identifier><identifier>PMID: 22827312</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adaptation, Physiological ; Alleles ; Animals ; Cyprinodontiformes - genetics ; Cyprinodontiformes - physiology ; ecological niche modelling ; elevation gradient ; Environment ; Evolutionary biology ; Female ; Fish ; Freshwater ; Gene Expression Regulation ; Gene Frequency ; Genetic markers ; Genetics, Population - methods ; Heat-Shock Proteins - analysis ; Heat-Shock Proteins - genetics ; Hot Temperature ; hybridization ; Hybridization, Genetic ; Male ; Morphology ; poeciliid ; Polymorphism, Single Nucleotide ; Population Dynamics ; population genetics ; Seasons ; Species Specificity ; Stress, Physiological ; Teleostei ; thermal tolerance ; Time Factors ; Viviparity, Nonmammalian ; Xiphophorus ; Xiphophorus birchmanni</subject><ispartof>Journal of evolutionary biology, 2012-09, Vol.25 (9), p.1800-1814</ispartof><rights>2012 The Authors. 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Hybrid zones between two poeciliid fishes, Xiphophorus birchmanni and X. malinche, occur in multiple tributaries with independent replication of upstream‐to‐downstream gradients in morphology and allele frequencies. Ecological niche modelling revealed that temperature is a central predictive factor in the spatial distribution of pure parental species and their hybrids and explains spatial and temporal variation in the frequency of neutral genetic markers in hybrid populations. Among populations of parentals and hybrids, both thermal tolerance and heat‐shock protein expression vary strongly, indicating that spatial and temporal structure is likely driven by adaptation to local thermal environments. Therefore, hybrid zone structure is strongly influenced by interspecific differences in physiological mechanisms for coping with the thermal environment.</description><subject>Adaptation, Physiological</subject><subject>Alleles</subject><subject>Animals</subject><subject>Cyprinodontiformes - genetics</subject><subject>Cyprinodontiformes - physiology</subject><subject>ecological niche modelling</subject><subject>elevation gradient</subject><subject>Environment</subject><subject>Evolutionary biology</subject><subject>Female</subject><subject>Fish</subject><subject>Freshwater</subject><subject>Gene Expression Regulation</subject><subject>Gene Frequency</subject><subject>Genetic markers</subject><subject>Genetics, Population - methods</subject><subject>Heat-Shock Proteins - analysis</subject><subject>Heat-Shock Proteins - genetics</subject><subject>Hot Temperature</subject><subject>hybridization</subject><subject>Hybridization, Genetic</subject><subject>Male</subject><subject>Morphology</subject><subject>poeciliid</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Population Dynamics</subject><subject>population genetics</subject><subject>Seasons</subject><subject>Species Specificity</subject><subject>Stress, Physiological</subject><subject>Teleostei</subject><subject>thermal tolerance</subject><subject>Time Factors</subject><subject>Viviparity, Nonmammalian</subject><subject>Xiphophorus</subject><subject>Xiphophorus birchmanni</subject><issn>1010-061X</issn><issn>1420-9101</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1v1DAQhiMEoqXwF5AlLuWQ4I84iZE4QFW-VAkORerN8tqTXa-8drAd2uXIL8fplh441bLkV5pnZmQ9VYUIbkg5b7YNaSmuBcGkoZjQBlPe0ebmUXV8X3hcMia4xh25OqqepbTFmHQt50-rI0oH2jNCj6s_3zf7ZIMLa6uVQ8qoKatsg0fKBb9G4H_ZGPwOfC7ldVTGlpiQ8gZFmFzpymDQZr-K1qDfwQNKOc46zxGQ9Shdh2iysi6h00twEFIG-xZd2WkTyo1zev28ejIql-DF3XtS_fh4fnn2ub749unL2fuLWvO2o7XGA-8F61tihGZ8pMIoDYqNoLkYuaakJZgbA8TwoQWxEoPihmK1Ukww3bGT6vQwd4rh5wwpy51NGpxTHsKcJMGCtT0bevYAlLFuoB1d0Ff_odswR18-ckvRXnDRF2o4UDqGlCKMcop2p-K-QHJRKrdyMScXc3JRKm-VypvS-vJuwbzagblv_OewAO8OwLV1sH_wYPn1_MOS2F8SvbFR</recordid><startdate>201209</startdate><enddate>201209</enddate><creator>Culumber, Z.W.</creator><creator>Shepard, D.B.</creator><creator>Coleman, S.W.</creator><creator>Rosenthal, G.G.</creator><creator>Tobler, M.</creator><general>Blackwell Publishing Ltd</general><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>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7TK</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope></search><sort><creationdate>201209</creationdate><title>Physiological adaptation along environmental gradients and replicated hybrid zone structure in swordtails (Teleostei: Xiphophorus)</title><author>Culumber, Z.W. ; 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subjects | Adaptation, Physiological Alleles Animals Cyprinodontiformes - genetics Cyprinodontiformes - physiology ecological niche modelling elevation gradient Environment Evolutionary biology Female Fish Freshwater Gene Expression Regulation Gene Frequency Genetic markers Genetics, Population - methods Heat-Shock Proteins - analysis Heat-Shock Proteins - genetics Hot Temperature hybridization Hybridization, Genetic Male Morphology poeciliid Polymorphism, Single Nucleotide Population Dynamics population genetics Seasons Species Specificity Stress, Physiological Teleostei thermal tolerance Time Factors Viviparity, Nonmammalian Xiphophorus Xiphophorus birchmanni |
title | Physiological adaptation along environmental gradients and replicated hybrid zone structure in swordtails (Teleostei: Xiphophorus) |
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