Phenotypic plasticity and adaptive evolution contribute to advancing flowering phenology in response to climate change
Anthropogenic climate change has already altered the timing of major life-history transitions, such as the initiation of reproduction. Both phenotypic plasticity and adaptive evolution can underlie rapid phenological shifts in response to climate change, but their relative contributions are poorly u...
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Veröffentlicht in: | Proceedings of the Royal Society. B, Biological sciences Biological sciences, 2012-09, Vol.279 (1743), p.3843-3852 |
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creator | Anderson, Jill T. Inouye, David W. McKinney, Amy M. Colautti, Robert I. Mitchell-Olds, Tom |
description | Anthropogenic climate change has already altered the timing of major life-history transitions, such as the initiation of reproduction. Both phenotypic plasticity and adaptive evolution can underlie rapid phenological shifts in response to climate change, but their relative contributions are poorly understood. Here, we combine a continuous 38 year field survey with quantitative genetic field experiments to assess adaptation in the context of climate change. We focused on Boechera stricta (Brassicaeae), a mustard native to the US Rocky Mountains. Flowering phenology advanced significantly from 1973 to 2011, and was strongly associated with warmer temperatures and earlier snowmelt dates. Strong directional selection favoured earlier flowering in contemporary environments (2010–2011). Climate change could drive this directional selection, and promote even earlier flowering as temperatures continue to increase. Our quantitative genetic analyses predict a response to selection of 0.2 to 0.5 days acceleration in flowering per generation, which could account for more than 20 per cent of the phenological change observed in the long-term dataset. However, the strength of directional selection and the predicted evolutionary response are likely much greater now than even 30 years ago because of rapidly changing climatic conditions. We predict that adaptation will likely be necessary for long-term in situ persistence in the context of climate change. |
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Both phenotypic plasticity and adaptive evolution can underlie rapid phenological shifts in response to climate change, but their relative contributions are poorly understood. Here, we combine a continuous 38 year field survey with quantitative genetic field experiments to assess adaptation in the context of climate change. We focused on Boechera stricta (Brassicaeae), a mustard native to the US Rocky Mountains. Flowering phenology advanced significantly from 1973 to 2011, and was strongly associated with warmer temperatures and earlier snowmelt dates. Strong directional selection favoured earlier flowering in contemporary environments (2010–2011). Climate change could drive this directional selection, and promote even earlier flowering as temperatures continue to increase. Our quantitative genetic analyses predict a response to selection of 0.2 to 0.5 days acceleration in flowering per generation, which could account for more than 20 per cent of the phenological change observed in the long-term dataset. However, the strength of directional selection and the predicted evolutionary response are likely much greater now than even 30 years ago because of rapidly changing climatic conditions. We predict that adaptation will likely be necessary for long-term in situ persistence in the context of climate change.</description><identifier>ISSN: 0962-8452</identifier><identifier>EISSN: 1471-2945</identifier><identifier>EISSN: 1471-2954</identifier><identifier>DOI: 10.1098/rspb.2012.1051</identifier><identifier>PMID: 22787021</identifier><language>eng</language><publisher>England: The Royal Society</publisher><subject>Adaptation, Physiological ; Adaptive Evolution ; Biological Evolution ; Boechera stricta ; Brassicaceae - genetics ; Brassicaceae - physiology ; Climate change ; Climate change adaptation ; Colorado ; Crosses, Genetic ; Evolution ; Evolutionary genetics ; Flowering ; Flowering Phenology ; Flowers - genetics ; Flowers - physiology ; Global Warming ; Inbreeding ; Materials ; Natural Selection ; Phenology ; Phenotype ; Phenotypic traits ; Plants ; Recombination, Genetic ; Reproduction ; Response To Selection ; Rocky Mountain Biological Laboratory ; Seasons ; Selection, Genetic ; Snowmelt ; Stricta ; Time Factors</subject><ispartof>Proceedings of the Royal Society. B, Biological sciences, 2012-09, Vol.279 (1743), p.3843-3852</ispartof><rights>Copyright © 2012 The Royal Society</rights><rights>This journal is © 2012 The Royal Society</rights><rights>This journal is © 2012 The Royal Society 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c593t-5d084cc133f0adc3e7311f47299d31004985dba795f45b2bfe455631cc2aea733</citedby><cites>FETCH-LOGICAL-c593t-5d084cc133f0adc3e7311f47299d31004985dba795f45b2bfe455631cc2aea733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/41727378$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/41727378$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22787021$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anderson, Jill T.</creatorcontrib><creatorcontrib>Inouye, David W.</creatorcontrib><creatorcontrib>McKinney, Amy M.</creatorcontrib><creatorcontrib>Colautti, Robert I.</creatorcontrib><creatorcontrib>Mitchell-Olds, Tom</creatorcontrib><title>Phenotypic plasticity and adaptive evolution contribute to advancing flowering phenology in response to climate change</title><title>Proceedings of the Royal Society. B, Biological sciences</title><addtitle>Proc. R. Soc. B</addtitle><addtitle>Proc. R. Soc. B</addtitle><description>Anthropogenic climate change has already altered the timing of major life-history transitions, such as the initiation of reproduction. Both phenotypic plasticity and adaptive evolution can underlie rapid phenological shifts in response to climate change, but their relative contributions are poorly understood. Here, we combine a continuous 38 year field survey with quantitative genetic field experiments to assess adaptation in the context of climate change. We focused on Boechera stricta (Brassicaeae), a mustard native to the US Rocky Mountains. Flowering phenology advanced significantly from 1973 to 2011, and was strongly associated with warmer temperatures and earlier snowmelt dates. Strong directional selection favoured earlier flowering in contemporary environments (2010–2011). Climate change could drive this directional selection, and promote even earlier flowering as temperatures continue to increase. Our quantitative genetic analyses predict a response to selection of 0.2 to 0.5 days acceleration in flowering per generation, which could account for more than 20 per cent of the phenological change observed in the long-term dataset. However, the strength of directional selection and the predicted evolutionary response are likely much greater now than even 30 years ago because of rapidly changing climatic conditions. We predict that adaptation will likely be necessary for long-term in situ persistence in the context of climate change.</description><subject>Adaptation, Physiological</subject><subject>Adaptive Evolution</subject><subject>Biological Evolution</subject><subject>Boechera stricta</subject><subject>Brassicaceae - genetics</subject><subject>Brassicaceae - physiology</subject><subject>Climate change</subject><subject>Climate change adaptation</subject><subject>Colorado</subject><subject>Crosses, Genetic</subject><subject>Evolution</subject><subject>Evolutionary genetics</subject><subject>Flowering</subject><subject>Flowering Phenology</subject><subject>Flowers - genetics</subject><subject>Flowers - physiology</subject><subject>Global Warming</subject><subject>Inbreeding</subject><subject>Materials</subject><subject>Natural Selection</subject><subject>Phenology</subject><subject>Phenotype</subject><subject>Phenotypic traits</subject><subject>Plants</subject><subject>Recombination, Genetic</subject><subject>Reproduction</subject><subject>Response To Selection</subject><subject>Rocky Mountain Biological Laboratory</subject><subject>Seasons</subject><subject>Selection, Genetic</subject><subject>Snowmelt</subject><subject>Stricta</subject><subject>Time Factors</subject><issn>0962-8452</issn><issn>1471-2945</issn><issn>1471-2954</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUuP0zAUhS0EYsrAlh0oSzYpfjb2BglGMEWqxEM8JDaW4zitS2oH28mQf49DhgoWrOyr893jIx8AHiO4RlDw5yH29RpDhPPI0B2wQrRCJRaU3QUrKDa45JThC_AgxiOEUDDO7oMLjCteQYxWYHx_MM6nqbe66DsVk9U2TYVyTaEa1Sc7msKMvhuS9a7Q3qVg6yGZIvkMjMpp6_ZF2_kbE-ZbP9t1fj8V1hXBxN67-BvWnT2pvKcPyu3NQ3CvVV00j27PS_D5zetPV9ty9-767dXLXamZIKlkDeRUa0RIC1WjiakIQi2tsBANQRBSwVlTq0qwlrIa162hjG0I0horoypCLsGLxbcf6pNptMn5VSf7kMOESXpl5b-Kswe596MkFDGBaDZ4dmsQ_I_BxCRPNmrTdcoZP0SJGEMbijjnGV0vqA4-xmDa8zMIyrksOZcl57LkXFZeePp3uDP-p50MkAUIfsq_5LU1aZJHPwSXx__bPlm2jjH5cHalqMIVqeac5aLbmMzPs67Cd7nJAJNfOJXftvjrxw-7rXxFfgF5Xr7K</recordid><startdate>20120922</startdate><enddate>20120922</enddate><creator>Anderson, Jill T.</creator><creator>Inouye, David W.</creator><creator>McKinney, Amy M.</creator><creator>Colautti, Robert I.</creator><creator>Mitchell-Olds, Tom</creator><general>The Royal Society</general><scope>BSCLL</scope><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>7SN</scope><scope>7ST</scope><scope>7U6</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>20120922</creationdate><title>Phenotypic plasticity and adaptive evolution contribute to advancing flowering phenology in response to climate change</title><author>Anderson, Jill T. ; Inouye, David W. ; McKinney, Amy M. ; Colautti, Robert I. ; Mitchell-Olds, Tom</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c593t-5d084cc133f0adc3e7311f47299d31004985dba795f45b2bfe455631cc2aea733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adaptation, Physiological</topic><topic>Adaptive Evolution</topic><topic>Biological Evolution</topic><topic>Boechera stricta</topic><topic>Brassicaceae - genetics</topic><topic>Brassicaceae - physiology</topic><topic>Climate change</topic><topic>Climate change adaptation</topic><topic>Colorado</topic><topic>Crosses, Genetic</topic><topic>Evolution</topic><topic>Evolutionary genetics</topic><topic>Flowering</topic><topic>Flowering Phenology</topic><topic>Flowers - genetics</topic><topic>Flowers - physiology</topic><topic>Global Warming</topic><topic>Inbreeding</topic><topic>Materials</topic><topic>Natural Selection</topic><topic>Phenology</topic><topic>Phenotype</topic><topic>Phenotypic traits</topic><topic>Plants</topic><topic>Recombination, Genetic</topic><topic>Reproduction</topic><topic>Response To Selection</topic><topic>Rocky Mountain Biological Laboratory</topic><topic>Seasons</topic><topic>Selection, Genetic</topic><topic>Snowmelt</topic><topic>Stricta</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anderson, Jill T.</creatorcontrib><creatorcontrib>Inouye, David W.</creatorcontrib><creatorcontrib>McKinney, Amy M.</creatorcontrib><creatorcontrib>Colautti, Robert I.</creatorcontrib><creatorcontrib>Mitchell-Olds, Tom</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Ecology Abstracts</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the Royal Society. B, Biological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anderson, Jill T.</au><au>Inouye, David W.</au><au>McKinney, Amy M.</au><au>Colautti, Robert I.</au><au>Mitchell-Olds, Tom</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phenotypic plasticity and adaptive evolution contribute to advancing flowering phenology in response to climate change</atitle><jtitle>Proceedings of the Royal Society. B, Biological sciences</jtitle><stitle>Proc. R. Soc. B</stitle><addtitle>Proc. R. Soc. B</addtitle><date>2012-09-22</date><risdate>2012</risdate><volume>279</volume><issue>1743</issue><spage>3843</spage><epage>3852</epage><pages>3843-3852</pages><issn>0962-8452</issn><eissn>1471-2945</eissn><eissn>1471-2954</eissn><abstract>Anthropogenic climate change has already altered the timing of major life-history transitions, such as the initiation of reproduction. Both phenotypic plasticity and adaptive evolution can underlie rapid phenological shifts in response to climate change, but their relative contributions are poorly understood. Here, we combine a continuous 38 year field survey with quantitative genetic field experiments to assess adaptation in the context of climate change. We focused on Boechera stricta (Brassicaeae), a mustard native to the US Rocky Mountains. Flowering phenology advanced significantly from 1973 to 2011, and was strongly associated with warmer temperatures and earlier snowmelt dates. Strong directional selection favoured earlier flowering in contemporary environments (2010–2011). Climate change could drive this directional selection, and promote even earlier flowering as temperatures continue to increase. Our quantitative genetic analyses predict a response to selection of 0.2 to 0.5 days acceleration in flowering per generation, which could account for more than 20 per cent of the phenological change observed in the long-term dataset. However, the strength of directional selection and the predicted evolutionary response are likely much greater now than even 30 years ago because of rapidly changing climatic conditions. We predict that adaptation will likely be necessary for long-term in situ persistence in the context of climate change.</abstract><cop>England</cop><pub>The Royal Society</pub><pmid>22787021</pmid><doi>10.1098/rspb.2012.1051</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation, Physiological Adaptive Evolution Biological Evolution Boechera stricta Brassicaceae - genetics Brassicaceae - physiology Climate change Climate change adaptation Colorado Crosses, Genetic Evolution Evolutionary genetics Flowering Flowering Phenology Flowers - genetics Flowers - physiology Global Warming Inbreeding Materials Natural Selection Phenology Phenotype Phenotypic traits Plants Recombination, Genetic Reproduction Response To Selection Rocky Mountain Biological Laboratory Seasons Selection, Genetic Snowmelt Stricta Time Factors |
title | Phenotypic plasticity and adaptive evolution contribute to advancing flowering phenology in response to climate change |
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