A geographic mosaic of coevolution between Eurosta solidaginis (Fitch) and its host plant tall goldenrod Solidago altissima (L.)
A geographic mosaic of coevolution has produced local reciprocal adaptation in tall goldenrod, Solidago altissima (L.), and the goldenrod ball-gall fly, Eurosta solidaginis (Fitch 1855). The fly is selected to induce gall diameters that minimize mortality from natural enemies, and the plant is selec...
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Veröffentlicht in: | Evolution 2021-12, Vol.75 (12), p.3056-3070 |
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description | A geographic mosaic of coevolution has produced local reciprocal adaptation in tall goldenrod, Solidago altissima (L.), and the goldenrod ball-gall fly, Eurosta solidaginis (Fitch 1855). The fly is selected to induce gall diameters that minimize mortality from natural enemies, and the plant is selected to limit gall growth that reduces plant fitness. We conducted a double reciprocal transplant experiment where S. altissima and E. solidaginis from three sites were grown in gardens at each site to partition the gall morphology variation into fly genotype, plant genotype, and the environment components. The host plant gall diameter induced by each E. solidaginis population was adapted to inhibit local natural enemies from ovipositing on or consuming enclosed larvae. Reciprocally, increasing the gall size induced by the local fly population increased the resistance of the local plant host population to gall growth. Differences among sites in natural enemies produced a mosaic of hotspots of coevolutionary arms races between flies selecting for greater gall diameter and plants for smaller diameters, and coldspots where there is no selection on plant or fly for a change in gall diameter. In contrast, the geographic variations of gall length and gall shape were not due to coevolutionary interactions. |
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The fly is selected to induce gall diameters that minimize mortality from natural enemies, and the plant is selected to limit gall growth that reduces plant fitness. We conducted a double reciprocal transplant experiment where S. altissima and E. solidaginis from three sites were grown in gardens at each site to partition the gall morphology variation into fly genotype, plant genotype, and the environment components. The host plant gall diameter induced by each E. solidaginis population was adapted to inhibit local natural enemies from ovipositing on or consuming enclosed larvae. Reciprocally, increasing the gall size induced by the local fly population increased the resistance of the local plant host population to gall growth. Differences among sites in natural enemies produced a mosaic of hotspots of coevolutionary arms races between flies selecting for greater gall diameter and plants for smaller diameters, and coldspots where there is no selection on plant or fly for a change in gall diameter. In contrast, the geographic variations of gall length and gall shape were not due to coevolutionary interactions.</description><identifier>ISSN: 0014-3820</identifier><identifier>EISSN: 1558-5646</identifier><identifier>DOI: 10.1111/evo.14391</identifier><identifier>PMID: 34726264</identifier><language>eng</language><publisher>United States: Wiley</publisher><subject>Animals ; Coevolution ; Eurosta solidaginis ; Gall ; Genotypes ; geographic mosaic of coevolution ; Geographical variations ; Herbivores ; Host plants ; Larva ; Larvae ; local adaptation ; Mosaics ; Natural enemies ; ORIGINAL ARTICLE ; parasitoid ; Plants ; Solidago - genetics ; Solidago altissima ; Tephritidae ; tritrophic interactions</subject><ispartof>Evolution, 2021-12, Vol.75 (12), p.3056-3070</ispartof><rights>2021 The Authors. Evolution © 2021 The Society for the Study of Evolution</rights><rights>2021 The Authors. © 2021 The Society for the Study of Evolution.</rights><rights>2021 The Authors. Evolution © 2021 The Society for the Study of Evolution.</rights><rights>2021, Society for the Study of Evolution</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3701-f01ace3697ba28842d9c3a6a06365ff84bd8627947037ffb2ab58c8272b6bf253</cites><orcidid>0000-0001-5339-4945 ; 0000-0001-9132-0373</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/48645982$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/48645982$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,1417,27924,27925,45574,45575,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34726264$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Craig, Timothy P.</creatorcontrib><creatorcontrib>Itami, Joanne K.</creatorcontrib><title>A geographic mosaic of coevolution between Eurosta solidaginis (Fitch) and its host plant tall goldenrod Solidago altissima (L.)</title><title>Evolution</title><addtitle>Evolution</addtitle><description>A geographic mosaic of coevolution has produced local reciprocal adaptation in tall goldenrod, Solidago altissima (L.), and the goldenrod ball-gall fly, Eurosta solidaginis (Fitch 1855). The fly is selected to induce gall diameters that minimize mortality from natural enemies, and the plant is selected to limit gall growth that reduces plant fitness. We conducted a double reciprocal transplant experiment where S. altissima and E. solidaginis from three sites were grown in gardens at each site to partition the gall morphology variation into fly genotype, plant genotype, and the environment components. The host plant gall diameter induced by each E. solidaginis population was adapted to inhibit local natural enemies from ovipositing on or consuming enclosed larvae. Reciprocally, increasing the gall size induced by the local fly population increased the resistance of the local plant host population to gall growth. Differences among sites in natural enemies produced a mosaic of hotspots of coevolutionary arms races between flies selecting for greater gall diameter and plants for smaller diameters, and coldspots where there is no selection on plant or fly for a change in gall diameter. In contrast, the geographic variations of gall length and gall shape were not due to coevolutionary interactions.</description><subject>Animals</subject><subject>Coevolution</subject><subject>Eurosta solidaginis</subject><subject>Gall</subject><subject>Genotypes</subject><subject>geographic mosaic of coevolution</subject><subject>Geographical variations</subject><subject>Herbivores</subject><subject>Host plants</subject><subject>Larva</subject><subject>Larvae</subject><subject>local adaptation</subject><subject>Mosaics</subject><subject>Natural enemies</subject><subject>ORIGINAL ARTICLE</subject><subject>parasitoid</subject><subject>Plants</subject><subject>Solidago - genetics</subject><subject>Solidago altissima</subject><subject>Tephritidae</subject><subject>tritrophic interactions</subject><issn>0014-3820</issn><issn>1558-5646</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kTtv2zAUhYmiReO4HfoDWhDoYg9y-BJFjUHgtAUMZEjSlaAo0qZBiy5JJcjWnx4mSjIU6F3u8p1zHweALxitcKkzcxdWmNEWvwMzXNeiqjnj78EMIcwqKgg6Aacp7RFCbY3bj-CEsoZwwtkM_D2HWxO2UR13TsNDSKq0YKEOxdSP2YUBdibfGzPA9RhDygqm4F2vtm5wCS4uXda7JVRDD11OcFcIePRqyDAr7-E2-N4MMfTwelIFqHx2KbmDgovNavkJfLDKJ_P5pc_B7eX65uJntbn68evifFNp2iBcWYSVNpS3TaeIEIz0raaKK8Qpr60VrOsFJ03LGkQbazuiulpoQRrS8c6Sms7BYvI9xvBnNCnLg0va-LKqCWOSpG4JRUJwXNDv_6D7MMahbCcJR08zmsLOwXKidPlKisbKYyxHxQeJkXyKRZYPyudYCvvtxXHsDqZ_I19zKMDZBNw7bx7-7yTXv69eLb9Oin3KIb4pmOCsbgWhjyctoBo</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Craig, Timothy P.</creator><creator>Itami, Joanne K.</creator><general>Wiley</general><general>Oxford University Press</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5339-4945</orcidid><orcidid>https://orcid.org/0000-0001-9132-0373</orcidid></search><sort><creationdate>20211201</creationdate><title>A geographic mosaic of coevolution between Eurosta solidaginis (Fitch) and its host plant tall goldenrod Solidago altissima (L.)</title><author>Craig, Timothy P. ; Itami, Joanne K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3701-f01ace3697ba28842d9c3a6a06365ff84bd8627947037ffb2ab58c8272b6bf253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Coevolution</topic><topic>Eurosta solidaginis</topic><topic>Gall</topic><topic>Genotypes</topic><topic>geographic mosaic of coevolution</topic><topic>Geographical variations</topic><topic>Herbivores</topic><topic>Host plants</topic><topic>Larva</topic><topic>Larvae</topic><topic>local adaptation</topic><topic>Mosaics</topic><topic>Natural enemies</topic><topic>ORIGINAL ARTICLE</topic><topic>parasitoid</topic><topic>Plants</topic><topic>Solidago - genetics</topic><topic>Solidago altissima</topic><topic>Tephritidae</topic><topic>tritrophic interactions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Craig, Timothy P.</creatorcontrib><creatorcontrib>Itami, Joanne K.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</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>Evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Craig, Timothy P.</au><au>Itami, Joanne K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A geographic mosaic of coevolution between Eurosta solidaginis (Fitch) and its host plant tall goldenrod Solidago altissima (L.)</atitle><jtitle>Evolution</jtitle><addtitle>Evolution</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>75</volume><issue>12</issue><spage>3056</spage><epage>3070</epage><pages>3056-3070</pages><issn>0014-3820</issn><eissn>1558-5646</eissn><abstract>A geographic mosaic of coevolution has produced local reciprocal adaptation in tall goldenrod, Solidago altissima (L.), and the goldenrod ball-gall fly, Eurosta solidaginis (Fitch 1855). The fly is selected to induce gall diameters that minimize mortality from natural enemies, and the plant is selected to limit gall growth that reduces plant fitness. We conducted a double reciprocal transplant experiment where S. altissima and E. solidaginis from three sites were grown in gardens at each site to partition the gall morphology variation into fly genotype, plant genotype, and the environment components. The host plant gall diameter induced by each E. solidaginis population was adapted to inhibit local natural enemies from ovipositing on or consuming enclosed larvae. Reciprocally, increasing the gall size induced by the local fly population increased the resistance of the local plant host population to gall growth. Differences among sites in natural enemies produced a mosaic of hotspots of coevolutionary arms races between flies selecting for greater gall diameter and plants for smaller diameters, and coldspots where there is no selection on plant or fly for a change in gall diameter. In contrast, the geographic variations of gall length and gall shape were not due to coevolutionary interactions.</abstract><cop>United States</cop><pub>Wiley</pub><pmid>34726264</pmid><doi>10.1111/evo.14391</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0001-5339-4945</orcidid><orcidid>https://orcid.org/0000-0001-9132-0373</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Coevolution Eurosta solidaginis Gall Genotypes geographic mosaic of coevolution Geographical variations Herbivores Host plants Larva Larvae local adaptation Mosaics Natural enemies ORIGINAL ARTICLE parasitoid Plants Solidago - genetics Solidago altissima Tephritidae tritrophic interactions |
title | A geographic mosaic of coevolution between Eurosta solidaginis (Fitch) and its host plant tall goldenrod Solidago altissima (L.) |
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