Thermal adaptation and phenotypic plasticity in a warming world: Insights from common garden experiments on Alaskan sockeye salmon
An important unresolved question is how populations of coldwater‐dependent fishes will respond to rapidly warming water temperatures. For example, the culturally and economically important group, Pacific salmon (Oncorhynchus spp.), experience site‐specific thermal regimes during early development th...
Gespeichert in:
Veröffentlicht in: | Global change biology 2017-12, Vol.23 (12), p.5203-5217 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 5217 |
---|---|
container_issue | 12 |
container_start_page | 5203 |
container_title | Global change biology |
container_volume | 23 |
creator | Sparks, Morgan M. Westley, Peter A. H. Falke, Jeffrey A. Quinn, Thomas P. |
description | An important unresolved question is how populations of coldwater‐dependent fishes will respond to rapidly warming water temperatures. For example, the culturally and economically important group, Pacific salmon (Oncorhynchus spp.), experience site‐specific thermal regimes during early development that could be disrupted by warming. To test for thermal local adaptation and heritable phenotypic plasticity in Pacific salmon embryos, we measured the developmental rate, survival, and body size at hatching in two populations of sockeye salmon (Oncorhynchus nerka) that overlap in timing of spawning but incubate in contrasting natural thermal regimes. Using a split half‐sibling design, we exposed embryos of 10 families from each of two populations to variable and constant thermal regimes. These represented both experienced temperatures by each population, and predicted temperatures under plausible future conditions based on a warming scenario from the downscaled global climate model (MIROC A1B scenario). We did not find evidence of thermal local adaptation during the embryonic stage for developmental rate or survival. Within treatments, populations hatched within 1 day of each other, on average, and among treatments, did not differ in survival in response to temperature. We did detect plasticity to temperature; embryos developed 2.5 times longer (189 days) in the coolest regime compared to the warmest regime (74 days). We also detected variation in developmental rates among families within and among temperature regimes, indicating heritable plasticity. Families exhibited a strong positive relationship between thermal variability and phenotypic variability in developmental rate but body length and mass at hatching were largely insensitive to temperature. Overall, our results indicated a lack of thermal local adaptation, but a presence of plasticity in populations experiencing contrasting conditions, as well as family‐specific heritable plasticity that could facilitate adaptive change.
Using a common garden approach that uniquely accounts for natural thermal variability, we simultaneously tested for thermal local adaptation and heritable phenotypic plasticity and show that developmental rate is largely governed by plasticity that has a heritable family‐specific component. Taken as a whole, our study indicates that survival of this important ectothermic organism at this life history period may not be directly impacted by predicted thermal conditions and that heritabl |
doi_str_mv | 10.1111/gcb.13782 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1906465990</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1963050070</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3532-882f973f23232848586d519747f9777c03fe56b3cabe85419be0cd3b867ba3863</originalsourceid><addsrcrecordid>eNp1kU1PxCAQhonR-H3wDxgSL3qoQimUels3fiUmXvTcUDrdRVuo0M3aq79c1lUPJsIBMvPkyUxehI4oOafxXMx0dU5ZLtMNtEuZ4EmaSbG5-vMsoYSyHbQXwgshhKVEbKOdVHIpKBe76ONpDr5TLVa16gc1GGexsjXu52DdMPZG475VYTDaDCM2sYmXynfGzvDS-ba-xPc2mNl8CLjxrsPadV1UzJSvwWJ478GbDmxsx-okml6VxcHpVxgBB9VG-ABtNaoNcPj97qPnm-un6V3y8Hh7P508JJpxliZSpk2RsyZl8cpstUHNaZFneSznuSasAS4qplUFkme0qIDomlVS5JViUrB9dLr29t69LSAMZWeChrZVFtwilLQgIhO8KEhET_6gL27hbZwuUoIRTki-os7WlPYuBA9N2cdllR9LSspVMGUMpvwKJrLH38ZF1UH9S_4kEYGLNbA0LYz_m8rb6dVa-Qlbl5fQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1963050070</pqid></control><display><type>article</type><title>Thermal adaptation and phenotypic plasticity in a warming world: Insights from common garden experiments on Alaskan sockeye salmon</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Sparks, Morgan M. ; Westley, Peter A. H. ; Falke, Jeffrey A. ; Quinn, Thomas P.</creator><creatorcontrib>Sparks, Morgan M. ; Westley, Peter A. H. ; Falke, Jeffrey A. ; Quinn, Thomas P.</creatorcontrib><description>An important unresolved question is how populations of coldwater‐dependent fishes will respond to rapidly warming water temperatures. For example, the culturally and economically important group, Pacific salmon (Oncorhynchus spp.), experience site‐specific thermal regimes during early development that could be disrupted by warming. To test for thermal local adaptation and heritable phenotypic plasticity in Pacific salmon embryos, we measured the developmental rate, survival, and body size at hatching in two populations of sockeye salmon (Oncorhynchus nerka) that overlap in timing of spawning but incubate in contrasting natural thermal regimes. Using a split half‐sibling design, we exposed embryos of 10 families from each of two populations to variable and constant thermal regimes. These represented both experienced temperatures by each population, and predicted temperatures under plausible future conditions based on a warming scenario from the downscaled global climate model (MIROC A1B scenario). We did not find evidence of thermal local adaptation during the embryonic stage for developmental rate or survival. Within treatments, populations hatched within 1 day of each other, on average, and among treatments, did not differ in survival in response to temperature. We did detect plasticity to temperature; embryos developed 2.5 times longer (189 days) in the coolest regime compared to the warmest regime (74 days). We also detected variation in developmental rates among families within and among temperature regimes, indicating heritable plasticity. Families exhibited a strong positive relationship between thermal variability and phenotypic variability in developmental rate but body length and mass at hatching were largely insensitive to temperature. Overall, our results indicated a lack of thermal local adaptation, but a presence of plasticity in populations experiencing contrasting conditions, as well as family‐specific heritable plasticity that could facilitate adaptive change.
Using a common garden approach that uniquely accounts for natural thermal variability, we simultaneously tested for thermal local adaptation and heritable phenotypic plasticity and show that developmental rate is largely governed by plasticity that has a heritable family‐specific component. Taken as a whole, our study indicates that survival of this important ectothermic organism at this life history period may not be directly impacted by predicted thermal conditions and that heritable phenotypic plasticity may largely buffer these populations against the effects of warming.</description><identifier>ISSN: 1354-1013</identifier><identifier>EISSN: 1365-2486</identifier><identifier>DOI: 10.1111/gcb.13782</identifier><identifier>PMID: 28586156</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Acclimatization ; Adaptation ; Animal embryos ; Animals ; Body length ; Body Size ; Body temperature ; Bristol Bay ; Climate Change ; Climate models ; developmental phenology ; Developmental plasticity ; Embryos ; Fish ; Freshwater fishes ; Gardens & gardening ; Genetic variability ; gene × environment ; Hatching ; Oncorhynchus ; Oncorhynchus nerka ; Phenotypic plasticity ; Plastic properties ; Plasticity ; Populations ; reaction norm ; Salmon ; Salmon - physiology ; Spawning ; Survival ; Temperature ; Temperature effects ; Variability ; Water ; Water temperature</subject><ispartof>Global change biology, 2017-12, Vol.23 (12), p.5203-5217</ispartof><rights>Published 2017. This article is a U.S. Government work and is in the public domain in the USA.</rights><rights>Copyright © 2017 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3532-882f973f23232848586d519747f9777c03fe56b3cabe85419be0cd3b867ba3863</citedby><cites>FETCH-LOGICAL-c3532-882f973f23232848586d519747f9777c03fe56b3cabe85419be0cd3b867ba3863</cites><orcidid>0000-0003-0787-2218</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fgcb.13782$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fgcb.13782$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28586156$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sparks, Morgan M.</creatorcontrib><creatorcontrib>Westley, Peter A. H.</creatorcontrib><creatorcontrib>Falke, Jeffrey A.</creatorcontrib><creatorcontrib>Quinn, Thomas P.</creatorcontrib><title>Thermal adaptation and phenotypic plasticity in a warming world: Insights from common garden experiments on Alaskan sockeye salmon</title><title>Global change biology</title><addtitle>Glob Chang Biol</addtitle><description>An important unresolved question is how populations of coldwater‐dependent fishes will respond to rapidly warming water temperatures. For example, the culturally and economically important group, Pacific salmon (Oncorhynchus spp.), experience site‐specific thermal regimes during early development that could be disrupted by warming. To test for thermal local adaptation and heritable phenotypic plasticity in Pacific salmon embryos, we measured the developmental rate, survival, and body size at hatching in two populations of sockeye salmon (Oncorhynchus nerka) that overlap in timing of spawning but incubate in contrasting natural thermal regimes. Using a split half‐sibling design, we exposed embryos of 10 families from each of two populations to variable and constant thermal regimes. These represented both experienced temperatures by each population, and predicted temperatures under plausible future conditions based on a warming scenario from the downscaled global climate model (MIROC A1B scenario). We did not find evidence of thermal local adaptation during the embryonic stage for developmental rate or survival. Within treatments, populations hatched within 1 day of each other, on average, and among treatments, did not differ in survival in response to temperature. We did detect plasticity to temperature; embryos developed 2.5 times longer (189 days) in the coolest regime compared to the warmest regime (74 days). We also detected variation in developmental rates among families within and among temperature regimes, indicating heritable plasticity. Families exhibited a strong positive relationship between thermal variability and phenotypic variability in developmental rate but body length and mass at hatching were largely insensitive to temperature. Overall, our results indicated a lack of thermal local adaptation, but a presence of plasticity in populations experiencing contrasting conditions, as well as family‐specific heritable plasticity that could facilitate adaptive change.
Using a common garden approach that uniquely accounts for natural thermal variability, we simultaneously tested for thermal local adaptation and heritable phenotypic plasticity and show that developmental rate is largely governed by plasticity that has a heritable family‐specific component. Taken as a whole, our study indicates that survival of this important ectothermic organism at this life history period may not be directly impacted by predicted thermal conditions and that heritable phenotypic plasticity may largely buffer these populations against the effects of warming.</description><subject>Acclimatization</subject><subject>Adaptation</subject><subject>Animal embryos</subject><subject>Animals</subject><subject>Body length</subject><subject>Body Size</subject><subject>Body temperature</subject><subject>Bristol Bay</subject><subject>Climate Change</subject><subject>Climate models</subject><subject>developmental phenology</subject><subject>Developmental plasticity</subject><subject>Embryos</subject><subject>Fish</subject><subject>Freshwater fishes</subject><subject>Gardens & gardening</subject><subject>Genetic variability</subject><subject>gene × environment</subject><subject>Hatching</subject><subject>Oncorhynchus</subject><subject>Oncorhynchus nerka</subject><subject>Phenotypic plasticity</subject><subject>Plastic properties</subject><subject>Plasticity</subject><subject>Populations</subject><subject>reaction norm</subject><subject>Salmon</subject><subject>Salmon - physiology</subject><subject>Spawning</subject><subject>Survival</subject><subject>Temperature</subject><subject>Temperature effects</subject><subject>Variability</subject><subject>Water</subject><subject>Water temperature</subject><issn>1354-1013</issn><issn>1365-2486</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1PxCAQhonR-H3wDxgSL3qoQimUels3fiUmXvTcUDrdRVuo0M3aq79c1lUPJsIBMvPkyUxehI4oOafxXMx0dU5ZLtMNtEuZ4EmaSbG5-vMsoYSyHbQXwgshhKVEbKOdVHIpKBe76ONpDr5TLVa16gc1GGexsjXu52DdMPZG475VYTDaDCM2sYmXynfGzvDS-ba-xPc2mNl8CLjxrsPadV1UzJSvwWJ478GbDmxsx-okml6VxcHpVxgBB9VG-ABtNaoNcPj97qPnm-un6V3y8Hh7P508JJpxliZSpk2RsyZl8cpstUHNaZFneSznuSasAS4qplUFkme0qIDomlVS5JViUrB9dLr29t69LSAMZWeChrZVFtwilLQgIhO8KEhET_6gL27hbZwuUoIRTki-os7WlPYuBA9N2cdllR9LSspVMGUMpvwKJrLH38ZF1UH9S_4kEYGLNbA0LYz_m8rb6dVa-Qlbl5fQ</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Sparks, Morgan M.</creator><creator>Westley, Peter A. H.</creator><creator>Falke, Jeffrey A.</creator><creator>Quinn, Thomas P.</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>7SN</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H97</scope><scope>L.G</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0787-2218</orcidid></search><sort><creationdate>201712</creationdate><title>Thermal adaptation and phenotypic plasticity in a warming world: Insights from common garden experiments on Alaskan sockeye salmon</title><author>Sparks, Morgan M. ; Westley, Peter A. H. ; Falke, Jeffrey A. ; Quinn, Thomas P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3532-882f973f23232848586d519747f9777c03fe56b3cabe85419be0cd3b867ba3863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acclimatization</topic><topic>Adaptation</topic><topic>Animal embryos</topic><topic>Animals</topic><topic>Body length</topic><topic>Body Size</topic><topic>Body temperature</topic><topic>Bristol Bay</topic><topic>Climate Change</topic><topic>Climate models</topic><topic>developmental phenology</topic><topic>Developmental plasticity</topic><topic>Embryos</topic><topic>Fish</topic><topic>Freshwater fishes</topic><topic>Gardens & gardening</topic><topic>Genetic variability</topic><topic>gene × environment</topic><topic>Hatching</topic><topic>Oncorhynchus</topic><topic>Oncorhynchus nerka</topic><topic>Phenotypic plasticity</topic><topic>Plastic properties</topic><topic>Plasticity</topic><topic>Populations</topic><topic>reaction norm</topic><topic>Salmon</topic><topic>Salmon - physiology</topic><topic>Spawning</topic><topic>Survival</topic><topic>Temperature</topic><topic>Temperature effects</topic><topic>Variability</topic><topic>Water</topic><topic>Water temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sparks, Morgan M.</creatorcontrib><creatorcontrib>Westley, Peter A. H.</creatorcontrib><creatorcontrib>Falke, Jeffrey A.</creatorcontrib><creatorcontrib>Quinn, Thomas P.</creatorcontrib><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>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><jtitle>Global change biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sparks, Morgan M.</au><au>Westley, Peter A. H.</au><au>Falke, Jeffrey A.</au><au>Quinn, Thomas P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thermal adaptation and phenotypic plasticity in a warming world: Insights from common garden experiments on Alaskan sockeye salmon</atitle><jtitle>Global change biology</jtitle><addtitle>Glob Chang Biol</addtitle><date>2017-12</date><risdate>2017</risdate><volume>23</volume><issue>12</issue><spage>5203</spage><epage>5217</epage><pages>5203-5217</pages><issn>1354-1013</issn><eissn>1365-2486</eissn><abstract>An important unresolved question is how populations of coldwater‐dependent fishes will respond to rapidly warming water temperatures. For example, the culturally and economically important group, Pacific salmon (Oncorhynchus spp.), experience site‐specific thermal regimes during early development that could be disrupted by warming. To test for thermal local adaptation and heritable phenotypic plasticity in Pacific salmon embryos, we measured the developmental rate, survival, and body size at hatching in two populations of sockeye salmon (Oncorhynchus nerka) that overlap in timing of spawning but incubate in contrasting natural thermal regimes. Using a split half‐sibling design, we exposed embryos of 10 families from each of two populations to variable and constant thermal regimes. These represented both experienced temperatures by each population, and predicted temperatures under plausible future conditions based on a warming scenario from the downscaled global climate model (MIROC A1B scenario). We did not find evidence of thermal local adaptation during the embryonic stage for developmental rate or survival. Within treatments, populations hatched within 1 day of each other, on average, and among treatments, did not differ in survival in response to temperature. We did detect plasticity to temperature; embryos developed 2.5 times longer (189 days) in the coolest regime compared to the warmest regime (74 days). We also detected variation in developmental rates among families within and among temperature regimes, indicating heritable plasticity. Families exhibited a strong positive relationship between thermal variability and phenotypic variability in developmental rate but body length and mass at hatching were largely insensitive to temperature. Overall, our results indicated a lack of thermal local adaptation, but a presence of plasticity in populations experiencing contrasting conditions, as well as family‐specific heritable plasticity that could facilitate adaptive change.
Using a common garden approach that uniquely accounts for natural thermal variability, we simultaneously tested for thermal local adaptation and heritable phenotypic plasticity and show that developmental rate is largely governed by plasticity that has a heritable family‐specific component. Taken as a whole, our study indicates that survival of this important ectothermic organism at this life history period may not be directly impacted by predicted thermal conditions and that heritable phenotypic plasticity may largely buffer these populations against the effects of warming.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>28586156</pmid><doi>10.1111/gcb.13782</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-0787-2218</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1354-1013 |
ispartof | Global change biology, 2017-12, Vol.23 (12), p.5203-5217 |
issn | 1354-1013 1365-2486 |
language | eng |
recordid | cdi_proquest_miscellaneous_1906465990 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Acclimatization Adaptation Animal embryos Animals Body length Body Size Body temperature Bristol Bay Climate Change Climate models developmental phenology Developmental plasticity Embryos Fish Freshwater fishes Gardens & gardening Genetic variability gene × environment Hatching Oncorhynchus Oncorhynchus nerka Phenotypic plasticity Plastic properties Plasticity Populations reaction norm Salmon Salmon - physiology Spawning Survival Temperature Temperature effects Variability Water Water temperature |
title | Thermal adaptation and phenotypic plasticity in a warming world: Insights from common garden experiments on Alaskan sockeye salmon |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T14%3A49%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Thermal%20adaptation%20and%20phenotypic%20plasticity%20in%20a%20warming%20world:%20Insights%20from%20common%20garden%20experiments%20on%20Alaskan%20sockeye%20salmon&rft.jtitle=Global%20change%20biology&rft.au=Sparks,%20Morgan%20M.&rft.date=2017-12&rft.volume=23&rft.issue=12&rft.spage=5203&rft.epage=5217&rft.pages=5203-5217&rft.issn=1354-1013&rft.eissn=1365-2486&rft_id=info:doi/10.1111/gcb.13782&rft_dat=%3Cproquest_cross%3E1963050070%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1963050070&rft_id=info:pmid/28586156&rfr_iscdi=true |