Short‐range phenotypic divergence among genetically distinct parapatric populations of an Australian funnel‐web spider
Speciation involves divergence at genetic and phenotypic levels. Where substantial genetic differentiation exists among populations, examining variation in multiple phenotypic characters may elucidate the mechanisms by which divergence and speciation unfold. Previous work on the Australian funnel‐we...
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description | Speciation involves divergence at genetic and phenotypic levels. Where substantial genetic differentiation exists among populations, examining variation in multiple phenotypic characters may elucidate the mechanisms by which divergence and speciation unfold. Previous work on the Australian funnel‐web spider Atrax sutherlandi Gray (2010; Records of the Australian Museum 62, 285–392; Mygalomorphae: Hexathelidae: Atracinae) has revealed a marked genetic structure along a 110‐kilometer transect, with six genetically distinct, parapatric populations attributable to past glacial cycles. In the present study, we explore variation in three classes of phenotypic characters (metabolic rate, water loss, and morphological traits) within the context of this phylogeographic structuring. Variation in metabolic and water loss rates shows no detectable association with genetic structure; the little variation observed in these rates may be due to the spiders’ behavioral adaptations (i.e., burrowing), which buffer the effects of climatic gradients across the landscape. However, of 17 morphological traits measured, 10 show significant variation among genetic populations, in a disjunct manner that is clearly not latitudinal. Moreover, patterns of variation observed for morphological traits serving different organismic functions (e.g., prey capture, burrowing, and locomotion) are dissimilar. In contrast, a previous study of an ecologically similar sympatric spider with little genetic structure indicated a strong latitudinal response in 10 traits over the same range. The congruence of morphological variation with deep phylogeographic structure in Tallaganda's A. sutherlandi populations, as well as the inconsistent patterns of variation across separate functional traits, suggest that the spiders are likely in early stages of speciation, with parapatric populations independently responding to local selective forces.
We examined variation in the physiology and morphology of parapatric spider populations showing phylogeographic structure. Although behavioral adaptions may account for low physiological variation overall, morphological traits differentiate according to phylogeographic boundaries. Disjunct patterns of variation among separate functional traits suggest that the genetically distinct populations may respond to local selective forces. |
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We examined variation in the physiology and morphology of parapatric spider populations showing phylogeographic structure. Although behavioral adaptions may account for low physiological variation overall, morphological traits differentiate according to phylogeographic boundaries. Disjunct patterns of variation among separate functional traits suggest that the genetically distinct populations may respond to local selective forces.</description><identifier>ISSN: 2045-7758</identifier><identifier>EISSN: 2045-7758</identifier><identifier>DOI: 10.1002/ece3.3084</identifier><identifier>PMID: 28770049</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Adaptation ; Atrax sutherlandi ; Divergence ; Ecological monitoring ; functional traits ; Genetic diversity ; Genetic structure ; Locomotion ; Metabolic rate ; Metabolism ; Morphology ; mygalomorph ; Original Research ; Parapatric populations ; Phenotypic variations ; Phylogeography ; physiology ; Population genetics ; Populations ; Prey ; Speciation ; Spiders ; Sympatric populations ; Tallaganda ; Water loss</subject><ispartof>Ecology and evolution, 2017-07, Vol.7 (14), p.5094-5102</ispartof><rights>2017 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4434-24cff89b64eb76664c53bf463c45dacffe1057809fbf25fa5d47e83c81b14aa33</citedby><cites>FETCH-LOGICAL-c4434-24cff89b64eb76664c53bf463c45dacffe1057809fbf25fa5d47e83c81b14aa33</cites><orcidid>0000-0002-6248-3103</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5528234/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5528234/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1417,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28770049$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wong, Mark K. L.</creatorcontrib><creatorcontrib>Woodman, James D.</creatorcontrib><creatorcontrib>Rowell, David M.</creatorcontrib><title>Short‐range phenotypic divergence among genetically distinct parapatric populations of an Australian funnel‐web spider</title><title>Ecology and evolution</title><addtitle>Ecol Evol</addtitle><description>Speciation involves divergence at genetic and phenotypic levels. Where substantial genetic differentiation exists among populations, examining variation in multiple phenotypic characters may elucidate the mechanisms by which divergence and speciation unfold. Previous work on the Australian funnel‐web spider Atrax sutherlandi Gray (2010; Records of the Australian Museum 62, 285–392; Mygalomorphae: Hexathelidae: Atracinae) has revealed a marked genetic structure along a 110‐kilometer transect, with six genetically distinct, parapatric populations attributable to past glacial cycles. In the present study, we explore variation in three classes of phenotypic characters (metabolic rate, water loss, and morphological traits) within the context of this phylogeographic structuring. Variation in metabolic and water loss rates shows no detectable association with genetic structure; the little variation observed in these rates may be due to the spiders’ behavioral adaptations (i.e., burrowing), which buffer the effects of climatic gradients across the landscape. However, of 17 morphological traits measured, 10 show significant variation among genetic populations, in a disjunct manner that is clearly not latitudinal. Moreover, patterns of variation observed for morphological traits serving different organismic functions (e.g., prey capture, burrowing, and locomotion) are dissimilar. In contrast, a previous study of an ecologically similar sympatric spider with little genetic structure indicated a strong latitudinal response in 10 traits over the same range. The congruence of morphological variation with deep phylogeographic structure in Tallaganda's A. sutherlandi populations, as well as the inconsistent patterns of variation across separate functional traits, suggest that the spiders are likely in early stages of speciation, with parapatric populations independently responding to local selective forces.
We examined variation in the physiology and morphology of parapatric spider populations showing phylogeographic structure. Although behavioral adaptions may account for low physiological variation overall, morphological traits differentiate according to phylogeographic boundaries. Disjunct patterns of variation among separate functional traits suggest that the genetically distinct populations may respond to local selective forces.</description><subject>Adaptation</subject><subject>Atrax sutherlandi</subject><subject>Divergence</subject><subject>Ecological monitoring</subject><subject>functional traits</subject><subject>Genetic diversity</subject><subject>Genetic structure</subject><subject>Locomotion</subject><subject>Metabolic rate</subject><subject>Metabolism</subject><subject>Morphology</subject><subject>mygalomorph</subject><subject>Original Research</subject><subject>Parapatric populations</subject><subject>Phenotypic variations</subject><subject>Phylogeography</subject><subject>physiology</subject><subject>Population genetics</subject><subject>Populations</subject><subject>Prey</subject><subject>Speciation</subject><subject>Spiders</subject><subject>Sympatric populations</subject><subject>Tallaganda</subject><subject>Water loss</subject><issn>2045-7758</issn><issn>2045-7758</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kc9qFTEYxYNYbGm78AUk4EYXt83kz2RmI5TLVQuFLqrrkMl8uTdlbhKTmZbrykfwGX0SM962VMFs8sH55XwnHIReV-SsIoSegwF2xkjDX6AjSrhYSCmal8_mQ3Sa8y0ppyaUE_kKHdJGSkJ4e4S-32xCGn_9-Jm0XwOOG_Bh3EVncO_uIK3BG8B6G_walxlGZ_Qw7IqYR-fNiKNOOuoxlQcxxGnQows-42Cx9vhiymPSgyujnbyHoey5hw7n6HpIJ-jA6iHD6cN9jL5-XH1Zfl5cXX-6XF5cLQznjC8oN9Y2bVdz6GRd19wI1lleM8NFr4sGFRGyIa3tLBVWi55LaJhpqq7iWjN2jD7sfePUbaE34OdQKia31Wmngnbqb8W7jVqHOyUEbSjjxeDdg0EK3ybIo9q6bGAYtIcwZVW1VDQtkaIu6Nt_0NswJV--pyhhBZBMzIbv95RJIecE9ilMRdRcqppLVXOphX3zPP0T-VhhAc73wL0bYPd_J7Vartgfy99LObDU</recordid><startdate>201707</startdate><enddate>201707</enddate><creator>Wong, Mark K. L.</creator><creator>Woodman, James D.</creator><creator>Rowell, David M.</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7X2</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M0K</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6248-3103</orcidid></search><sort><creationdate>201707</creationdate><title>Short‐range phenotypic divergence among genetically distinct parapatric populations of an Australian funnel‐web spider</title><author>Wong, Mark K. L. ; Woodman, James D. ; Rowell, David M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4434-24cff89b64eb76664c53bf463c45dacffe1057809fbf25fa5d47e83c81b14aa33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adaptation</topic><topic>Atrax sutherlandi</topic><topic>Divergence</topic><topic>Ecological monitoring</topic><topic>functional traits</topic><topic>Genetic diversity</topic><topic>Genetic structure</topic><topic>Locomotion</topic><topic>Metabolic rate</topic><topic>Metabolism</topic><topic>Morphology</topic><topic>mygalomorph</topic><topic>Original Research</topic><topic>Parapatric populations</topic><topic>Phenotypic variations</topic><topic>Phylogeography</topic><topic>physiology</topic><topic>Population genetics</topic><topic>Populations</topic><topic>Prey</topic><topic>Speciation</topic><topic>Spiders</topic><topic>Sympatric populations</topic><topic>Tallaganda</topic><topic>Water loss</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wong, Mark K. L.</creatorcontrib><creatorcontrib>Woodman, James D.</creatorcontrib><creatorcontrib>Rowell, David M.</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Ecology and evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wong, Mark K. L.</au><au>Woodman, James D.</au><au>Rowell, David M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Short‐range phenotypic divergence among genetically distinct parapatric populations of an Australian funnel‐web spider</atitle><jtitle>Ecology and evolution</jtitle><addtitle>Ecol Evol</addtitle><date>2017-07</date><risdate>2017</risdate><volume>7</volume><issue>14</issue><spage>5094</spage><epage>5102</epage><pages>5094-5102</pages><issn>2045-7758</issn><eissn>2045-7758</eissn><abstract>Speciation involves divergence at genetic and phenotypic levels. Where substantial genetic differentiation exists among populations, examining variation in multiple phenotypic characters may elucidate the mechanisms by which divergence and speciation unfold. Previous work on the Australian funnel‐web spider Atrax sutherlandi Gray (2010; Records of the Australian Museum 62, 285–392; Mygalomorphae: Hexathelidae: Atracinae) has revealed a marked genetic structure along a 110‐kilometer transect, with six genetically distinct, parapatric populations attributable to past glacial cycles. In the present study, we explore variation in three classes of phenotypic characters (metabolic rate, water loss, and morphological traits) within the context of this phylogeographic structuring. Variation in metabolic and water loss rates shows no detectable association with genetic structure; the little variation observed in these rates may be due to the spiders’ behavioral adaptations (i.e., burrowing), which buffer the effects of climatic gradients across the landscape. However, of 17 morphological traits measured, 10 show significant variation among genetic populations, in a disjunct manner that is clearly not latitudinal. Moreover, patterns of variation observed for morphological traits serving different organismic functions (e.g., prey capture, burrowing, and locomotion) are dissimilar. In contrast, a previous study of an ecologically similar sympatric spider with little genetic structure indicated a strong latitudinal response in 10 traits over the same range. The congruence of morphological variation with deep phylogeographic structure in Tallaganda's A. sutherlandi populations, as well as the inconsistent patterns of variation across separate functional traits, suggest that the spiders are likely in early stages of speciation, with parapatric populations independently responding to local selective forces.
We examined variation in the physiology and morphology of parapatric spider populations showing phylogeographic structure. Although behavioral adaptions may account for low physiological variation overall, morphological traits differentiate according to phylogeographic boundaries. Disjunct patterns of variation among separate functional traits suggest that the genetically distinct populations may respond to local selective forces.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>28770049</pmid><doi>10.1002/ece3.3084</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6248-3103</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation Atrax sutherlandi Divergence Ecological monitoring functional traits Genetic diversity Genetic structure Locomotion Metabolic rate Metabolism Morphology mygalomorph Original Research Parapatric populations Phenotypic variations Phylogeography physiology Population genetics Populations Prey Speciation Spiders Sympatric populations Tallaganda Water loss |
title | Short‐range phenotypic divergence among genetically distinct parapatric populations of an Australian funnel‐web spider |
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