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Biological traits yield divergent phylogeographical patterns between two aphids living on the same host plants
Aim: Animals' phylogeographical patterns are frequently explained by Pleistocene glacial fluctuations and topographical environments. However, speciesspecific biological traits are thought to have profound impacts on distribution patterns, particularly in aphids. We hypothesize that the phyloge...
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Published in: | Journal of biogeography 2017-02, Vol.44 (2), p.348-360 |
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description | Aim: Animals' phylogeographical patterns are frequently explained by Pleistocene glacial fluctuations and topographical environments. However, speciesspecific biological traits are thought to have profound impacts on distribution patterns, particularly in aphids. We hypothesize that the phylogeographical patterns and/or population dynamics of two sympatric aphids may be different due to their different reproductive modes and feeding sites, even though they share the same hosts and environmental conditions. Location: China. Methods: We explored our hypothesis in Chaitophorus saliniger and Tuberolachnus salignus, two aphids that share the same host plants (genus Salix) but differ biologically. Chaitophorus saliniger is characterized by alternating sexual and asexual reproduction and only feeds on willow leaves, whereas T. salignus has obligate asexual reproduction and feeds on trunks and branches. The genetic diversity, population structure and demographic history of the aphids were analysed based on both mitochondrial DNA (cytochrome c. oxidase subunit I and cytochrome b) and nuclear DNA (translation elongation factor 1 alpha). Ecological niche models (ENMs) were used to explore historical changes in distribution. The chief environmental variables that discriminate the different haplogroups were identified through multivariate statistical analysis. Results: There were striking differences in the phylogeographical patterns between the species. The sexual C. saliniger exhibited higher genetic diversity and population variations than the asexual T. salignus. According to genetic analyses and ENMs, both species experienced glacial contraction and post-glacial expansion. Multivariate statistical analysis revealed that the climatic differences between the divergent haplogroups were explained by principal components mainly loaded with temperature and elevation. Main conclusions: Our results suggest that species-specific biological traits and historical climate fluctuations have both shaped the current phylogeographical patterns of both aphid species. Their distinct genetic diversity and population structures highlight the importance of intrinsic biological features in driving phylogeographical patterns. |
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However, speciesspecific biological traits are thought to have profound impacts on distribution patterns, particularly in aphids. We hypothesize that the phylogeographical patterns and/or population dynamics of two sympatric aphids may be different due to their different reproductive modes and feeding sites, even though they share the same hosts and environmental conditions. Location: China. Methods: We explored our hypothesis in Chaitophorus saliniger and Tuberolachnus salignus, two aphids that share the same host plants (genus Salix) but differ biologically. Chaitophorus saliniger is characterized by alternating sexual and asexual reproduction and only feeds on willow leaves, whereas T. salignus has obligate asexual reproduction and feeds on trunks and branches. The genetic diversity, population structure and demographic history of the aphids were analysed based on both mitochondrial DNA (cytochrome c. oxidase subunit I and cytochrome b) and nuclear DNA (translation elongation factor 1 alpha). Ecological niche models (ENMs) were used to explore historical changes in distribution. The chief environmental variables that discriminate the different haplogroups were identified through multivariate statistical analysis. Results: There were striking differences in the phylogeographical patterns between the species. The sexual C. saliniger exhibited higher genetic diversity and population variations than the asexual T. salignus. According to genetic analyses and ENMs, both species experienced glacial contraction and post-glacial expansion. Multivariate statistical analysis revealed that the climatic differences between the divergent haplogroups were explained by principal components mainly loaded with temperature and elevation. Main conclusions: Our results suggest that species-specific biological traits and historical climate fluctuations have both shaped the current phylogeographical patterns of both aphid species. Their distinct genetic diversity and population structures highlight the importance of intrinsic biological features in driving phylogeographical patterns.</description><identifier>ISSN: 0305-0270</identifier><identifier>EISSN: 1365-2699</identifier><identifier>DOI: 10.1111/jbi.12818</identifier><identifier>CODEN: JBIODN</identifier><language>eng</language><publisher>Oxford: John Wiley & Sons Ltd</publisher><subject>Aphid ; Aphidoidea ; Asexual reproduction ; Biodiversity ; biological characteristic ; Chaitophorus saliniger ; Contraction ; Cytochrome ; Cytochrome b ; Cytochrome-c oxidase ; Demographics ; Deoxyribonucleic acid ; Distribution patterns ; DNA ; ecological modelling ; Ecological niches ; Elongation ; Environmental changes ; Environmental conditions ; Fluctuations ; Genetic analysis ; Genetic diversity ; Host plants ; Insects ; Leaves ; Mitochondrial DNA ; Multivariate statistical analysis ; phylogeographical patterns ; Plants (botany) ; Pleistocene ; Population ; Population (statistical) ; Population dynamics ; Population genetics ; Population structure ; Refuges ; Reproduction ; Reproduction (biology) ; Species ; Species diversity ; Statistical analysis ; Statistics ; Sympatric populations ; Translation elongation ; Tuberolachnus salignus ; Willow</subject><ispartof>Journal of biogeography, 2017-02, Vol.44 (2), p.348-360</ispartof><rights>Copyright © 2017 John Wiley & Sons Ltd.</rights><rights>2016 John Wiley & Sons Ltd</rights><rights>Copyright © 2017 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4138-e5ffaa1ef907ef56422e7a317069208a8349f379851f97b650134ed5652cdfd03</citedby><cites>FETCH-LOGICAL-c4138-e5ffaa1ef907ef56422e7a317069208a8349f379851f97b650134ed5652cdfd03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/44202785$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/44202785$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids></links><search><creatorcontrib>Fang, Fang</creatorcontrib><creatorcontrib>Chen, Jing</creatorcontrib><creatorcontrib>Jiang, Li-Yun</creatorcontrib><creatorcontrib>Chen, Rui</creatorcontrib><creatorcontrib>Qiao, Ge-Xia</creatorcontrib><title>Biological traits yield divergent phylogeographical patterns between two aphids living on the same host plants</title><title>Journal of biogeography</title><description>Aim: Animals' phylogeographical patterns are frequently explained by Pleistocene glacial fluctuations and topographical environments. However, speciesspecific biological traits are thought to have profound impacts on distribution patterns, particularly in aphids. We hypothesize that the phylogeographical patterns and/or population dynamics of two sympatric aphids may be different due to their different reproductive modes and feeding sites, even though they share the same hosts and environmental conditions. Location: China. Methods: We explored our hypothesis in Chaitophorus saliniger and Tuberolachnus salignus, two aphids that share the same host plants (genus Salix) but differ biologically. Chaitophorus saliniger is characterized by alternating sexual and asexual reproduction and only feeds on willow leaves, whereas T. salignus has obligate asexual reproduction and feeds on trunks and branches. The genetic diversity, population structure and demographic history of the aphids were analysed based on both mitochondrial DNA (cytochrome c. oxidase subunit I and cytochrome b) and nuclear DNA (translation elongation factor 1 alpha). Ecological niche models (ENMs) were used to explore historical changes in distribution. The chief environmental variables that discriminate the different haplogroups were identified through multivariate statistical analysis. Results: There were striking differences in the phylogeographical patterns between the species. The sexual C. saliniger exhibited higher genetic diversity and population variations than the asexual T. salignus. According to genetic analyses and ENMs, both species experienced glacial contraction and post-glacial expansion. Multivariate statistical analysis revealed that the climatic differences between the divergent haplogroups were explained by principal components mainly loaded with temperature and elevation. Main conclusions: Our results suggest that species-specific biological traits and historical climate fluctuations have both shaped the current phylogeographical patterns of both aphid species. Their distinct genetic diversity and population structures highlight the importance of intrinsic biological features in driving phylogeographical patterns.</description><subject>Aphid</subject><subject>Aphidoidea</subject><subject>Asexual reproduction</subject><subject>Biodiversity</subject><subject>biological characteristic</subject><subject>Chaitophorus saliniger</subject><subject>Contraction</subject><subject>Cytochrome</subject><subject>Cytochrome b</subject><subject>Cytochrome-c oxidase</subject><subject>Demographics</subject><subject>Deoxyribonucleic acid</subject><subject>Distribution patterns</subject><subject>DNA</subject><subject>ecological modelling</subject><subject>Ecological niches</subject><subject>Elongation</subject><subject>Environmental changes</subject><subject>Environmental conditions</subject><subject>Fluctuations</subject><subject>Genetic analysis</subject><subject>Genetic diversity</subject><subject>Host plants</subject><subject>Insects</subject><subject>Leaves</subject><subject>Mitochondrial DNA</subject><subject>Multivariate statistical analysis</subject><subject>phylogeographical patterns</subject><subject>Plants (botany)</subject><subject>Pleistocene</subject><subject>Population</subject><subject>Population (statistical)</subject><subject>Population dynamics</subject><subject>Population genetics</subject><subject>Population structure</subject><subject>Refuges</subject><subject>Reproduction</subject><subject>Reproduction (biology)</subject><subject>Species</subject><subject>Species diversity</subject><subject>Statistical analysis</subject><subject>Statistics</subject><subject>Sympatric populations</subject><subject>Translation elongation</subject><subject>Tuberolachnus salignus</subject><subject>Willow</subject><issn>0305-0270</issn><issn>1365-2699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kU1PIzEMhqMVSFs-DvsDVoq0Jw5DnWSSSY4LYvlQJS5wHqUdp001ncwmgar_flPKcgNfLNnPa8uvCfnB4JKVmK7n_pJxzfQ3MmFCyYorY47IBATICngD38lJSmsAMFLUEzJc-dCHpV_YnuZofU5057HvaOdfMS5xyHRc7QqBYRntuHoDR5szxiHROeYt4kDzNtB9s0u0969-WNJQiiukyW6QrkIqU3o75HRGjp3tE56_51Py_Ofm6fqumj3e3l__nlWLmgldoXTOWobOQINOqppzbKxgDSjDQVstauNEY7RkzjRzJYGJGjupJF90rgNxSn4d5o4x_H3BlNt1eIlDWdlyUHU5XhvzFcW0KjaCBlWoiwO1iCGliK4do9_YuGsZtHvT22J6-2Z6YacHdut73H0Otg9X9_8VPw-KdcohfijqmpdvaSn-AcJvjRc</recordid><startdate>201702</startdate><enddate>201702</enddate><creator>Fang, Fang</creator><creator>Chen, Jing</creator><creator>Jiang, Li-Yun</creator><creator>Chen, Rui</creator><creator>Qiao, Ge-Xia</creator><general>John Wiley & Sons Ltd</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>201702</creationdate><title>Biological traits yield divergent phylogeographical patterns between two aphids living on the same host plants</title><author>Fang, Fang ; Chen, Jing ; Jiang, Li-Yun ; Chen, Rui ; Qiao, Ge-Xia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4138-e5ffaa1ef907ef56422e7a317069208a8349f379851f97b650134ed5652cdfd03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aphid</topic><topic>Aphidoidea</topic><topic>Asexual reproduction</topic><topic>Biodiversity</topic><topic>biological characteristic</topic><topic>Chaitophorus saliniger</topic><topic>Contraction</topic><topic>Cytochrome</topic><topic>Cytochrome b</topic><topic>Cytochrome-c oxidase</topic><topic>Demographics</topic><topic>Deoxyribonucleic acid</topic><topic>Distribution patterns</topic><topic>DNA</topic><topic>ecological modelling</topic><topic>Ecological niches</topic><topic>Elongation</topic><topic>Environmental changes</topic><topic>Environmental conditions</topic><topic>Fluctuations</topic><topic>Genetic analysis</topic><topic>Genetic diversity</topic><topic>Host plants</topic><topic>Insects</topic><topic>Leaves</topic><topic>Mitochondrial DNA</topic><topic>Multivariate statistical analysis</topic><topic>phylogeographical patterns</topic><topic>Plants (botany)</topic><topic>Pleistocene</topic><topic>Population</topic><topic>Population (statistical)</topic><topic>Population dynamics</topic><topic>Population genetics</topic><topic>Population structure</topic><topic>Refuges</topic><topic>Reproduction</topic><topic>Reproduction (biology)</topic><topic>Species</topic><topic>Species diversity</topic><topic>Statistical analysis</topic><topic>Statistics</topic><topic>Sympatric populations</topic><topic>Translation elongation</topic><topic>Tuberolachnus salignus</topic><topic>Willow</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fang, Fang</creatorcontrib><creatorcontrib>Chen, Jing</creatorcontrib><creatorcontrib>Jiang, Li-Yun</creatorcontrib><creatorcontrib>Chen, Rui</creatorcontrib><creatorcontrib>Qiao, Ge-Xia</creatorcontrib><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>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Journal of biogeography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fang, Fang</au><au>Chen, Jing</au><au>Jiang, Li-Yun</au><au>Chen, Rui</au><au>Qiao, Ge-Xia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biological traits yield divergent phylogeographical patterns between two aphids living on the same host plants</atitle><jtitle>Journal of biogeography</jtitle><date>2017-02</date><risdate>2017</risdate><volume>44</volume><issue>2</issue><spage>348</spage><epage>360</epage><pages>348-360</pages><issn>0305-0270</issn><eissn>1365-2699</eissn><coden>JBIODN</coden><abstract>Aim: Animals' phylogeographical patterns are frequently explained by Pleistocene glacial fluctuations and topographical environments. However, speciesspecific biological traits are thought to have profound impacts on distribution patterns, particularly in aphids. We hypothesize that the phylogeographical patterns and/or population dynamics of two sympatric aphids may be different due to their different reproductive modes and feeding sites, even though they share the same hosts and environmental conditions. Location: China. Methods: We explored our hypothesis in Chaitophorus saliniger and Tuberolachnus salignus, two aphids that share the same host plants (genus Salix) but differ biologically. Chaitophorus saliniger is characterized by alternating sexual and asexual reproduction and only feeds on willow leaves, whereas T. salignus has obligate asexual reproduction and feeds on trunks and branches. The genetic diversity, population structure and demographic history of the aphids were analysed based on both mitochondrial DNA (cytochrome c. oxidase subunit I and cytochrome b) and nuclear DNA (translation elongation factor 1 alpha). Ecological niche models (ENMs) were used to explore historical changes in distribution. The chief environmental variables that discriminate the different haplogroups were identified through multivariate statistical analysis. Results: There were striking differences in the phylogeographical patterns between the species. The sexual C. saliniger exhibited higher genetic diversity and population variations than the asexual T. salignus. According to genetic analyses and ENMs, both species experienced glacial contraction and post-glacial expansion. Multivariate statistical analysis revealed that the climatic differences between the divergent haplogroups were explained by principal components mainly loaded with temperature and elevation. Main conclusions: Our results suggest that species-specific biological traits and historical climate fluctuations have both shaped the current phylogeographical patterns of both aphid species. Their distinct genetic diversity and population structures highlight the importance of intrinsic biological features in driving phylogeographical patterns.</abstract><cop>Oxford</cop><pub>John Wiley & Sons Ltd</pub><doi>10.1111/jbi.12818</doi><tpages>13</tpages></addata></record> |
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subjects | Aphid Aphidoidea Asexual reproduction Biodiversity biological characteristic Chaitophorus saliniger Contraction Cytochrome Cytochrome b Cytochrome-c oxidase Demographics Deoxyribonucleic acid Distribution patterns DNA ecological modelling Ecological niches Elongation Environmental changes Environmental conditions Fluctuations Genetic analysis Genetic diversity Host plants Insects Leaves Mitochondrial DNA Multivariate statistical analysis phylogeographical patterns Plants (botany) Pleistocene Population Population (statistical) Population dynamics Population genetics Population structure Refuges Reproduction Reproduction (biology) Species Species diversity Statistical analysis Statistics Sympatric populations Translation elongation Tuberolachnus salignus Willow |
title | Biological traits yield divergent phylogeographical patterns between two aphids living on the same host plants |
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