Climate mediates the trade‐offs associated with phenotypic plasticity in an amphibian polyphenism
Polyphenisms occur when phenotypic plasticity produces morphologically distinct phenotypes from the same genotype. Plasticity is maintained through fitness trade‐offs which are conferred to different phenotypes under specific environmental contexts. Predicting the impacts of contemporary climate cha...
Gespeichert in:
Veröffentlicht in: | The Journal of animal ecology 2024-11, Vol.93 (11), p.1747-1757 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1757 |
---|---|
container_issue | 11 |
container_start_page | 1747 |
container_title | The Journal of animal ecology |
container_volume | 93 |
creator | Kirk, Mark A. Lackey, Alycia C. R. Reider, Kelsey E. Thomas, Scott A. Whiteman, Howard H. |
description | Polyphenisms occur when phenotypic plasticity produces morphologically distinct phenotypes from the same genotype. Plasticity is maintained through fitness trade‐offs which are conferred to different phenotypes under specific environmental contexts. Predicting the impacts of contemporary climate change on phenotypic plasticity is critical for climate‐sensitive animals like amphibians, but elucidating the selective pressures maintaining polyphenisms requires a framework to control for all mechanistic drivers of plasticity.
Using a 32‐year dataset documenting the larval and adult histories of 717 Arizona tiger salamanders (Ambystoma mavortium nebulosum), we determined how annual variation in climate and density dependence explained the maintenance of two distinct morphs (terrestrial metamorph vs. aquatic paedomorph) in a high‐elevation polyphenism. The effects of climate and conspecific density on morph development were evaluated with piecewise structural equation models (SEM) to tease apart the direct and indirect pathways by which these two mechanisms affect phenotypic plasticity.
Climate had a direct effect on morph outcome whereby longer growing seasons favoured metamorphic outcomes. Also, climate had indirect effects on morph outcome as mediated through density‐dependent effects, such as long overwintering coldspells corresponding to high cannibal densities and light snowpacks corresponding to high larval densities, both of which promoted paedomorphic outcomes.
Both climate and density dependence serve as important proxies for growth and resource limitation, which are important underlying drivers of the phenotypic plasticity in animal polyphenisms. Our findings motivate new studies to determine how contemporary climate change will alter the selective pressures maintaining phenotypic plasticity and polyphenisms.
Our research provides important and novel insight into how climate change underlies the maintenance of phenotypic plasticity. |
doi_str_mv | 10.1111/1365-2656.14187 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3110913383</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3154170768</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2897-b8db31282ccb7639368e2ad0ca6673c3df18174b63ce663080433d1045f9a5fa3</originalsourceid><addsrcrecordid>eNqNkctOxCAUhonR6HhZuzMkbtxUOT0t0KWZjLcY3eiaUEozmHZaSyemOx_BZ_RJpM44CzdKSA6Bjz9wPkKOgZ1DGBeAPI1invJzSECKLTLZ7GyTCWMxRFJkbI_se__CGBMxw12yhxkmLPATYqaVq3VvaW0LF6qn_dzSvtOF_Xz_aMrSU-19Y8azgr65fk7buV00_dA6Q9tK-94Z1w_ULagOs27nLndh1TbVMJLO14dkp9SVt0frekCer2ZP05vo_vH6dnp5H5lYZiLKZZEjxDI2Jhc8PJFLG-uCGc25QINFCRJEknM0lnNkkiWIBbAkLTOdlhoPyNkqt-2a16X1vaqdN7aq9MI2S68Q0gQEE1z-AwWWAaLEgJ7-Ql-aZbcIHwlUnECWIIdAXawo0zXed7ZUbRca2w0KmBpVqVGMGsWob1Xhxsk6d5mH5m_4HzcB4CvgzVV2-CtP3V0-zFbJXxBlniE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3124194361</pqid></control><display><type>article</type><title>Climate mediates the trade‐offs associated with phenotypic plasticity in an amphibian polyphenism</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Kirk, Mark A. ; Lackey, Alycia C. R. ; Reider, Kelsey E. ; Thomas, Scott A. ; Whiteman, Howard H.</creator><creatorcontrib>Kirk, Mark A. ; Lackey, Alycia C. R. ; Reider, Kelsey E. ; Thomas, Scott A. ; Whiteman, Howard H.</creatorcontrib><description>Polyphenisms occur when phenotypic plasticity produces morphologically distinct phenotypes from the same genotype. Plasticity is maintained through fitness trade‐offs which are conferred to different phenotypes under specific environmental contexts. Predicting the impacts of contemporary climate change on phenotypic plasticity is critical for climate‐sensitive animals like amphibians, but elucidating the selective pressures maintaining polyphenisms requires a framework to control for all mechanistic drivers of plasticity.
Using a 32‐year dataset documenting the larval and adult histories of 717 Arizona tiger salamanders (Ambystoma mavortium nebulosum), we determined how annual variation in climate and density dependence explained the maintenance of two distinct morphs (terrestrial metamorph vs. aquatic paedomorph) in a high‐elevation polyphenism. The effects of climate and conspecific density on morph development were evaluated with piecewise structural equation models (SEM) to tease apart the direct and indirect pathways by which these two mechanisms affect phenotypic plasticity.
Climate had a direct effect on morph outcome whereby longer growing seasons favoured metamorphic outcomes. Also, climate had indirect effects on morph outcome as mediated through density‐dependent effects, such as long overwintering coldspells corresponding to high cannibal densities and light snowpacks corresponding to high larval densities, both of which promoted paedomorphic outcomes.
Both climate and density dependence serve as important proxies for growth and resource limitation, which are important underlying drivers of the phenotypic plasticity in animal polyphenisms. Our findings motivate new studies to determine how contemporary climate change will alter the selective pressures maintaining phenotypic plasticity and polyphenisms.
Our research provides important and novel insight into how climate change underlies the maintenance of phenotypic plasticity.</description><identifier>ISSN: 0021-8790</identifier><identifier>ISSN: 1365-2656</identifier><identifier>EISSN: 1365-2656</identifier><identifier>DOI: 10.1111/1365-2656.14187</identifier><identifier>PMID: 39340187</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adaptation, Physiological ; adults ; Ambystoma ; Ambystoma - genetics ; Ambystoma - physiology ; Ambystoma mavortium nebulosum ; Amphibians ; animal ecology ; Animals ; Annual variations ; Arizona ; Climate ; Climate Change ; Climate effects ; Climate models ; Climate prediction ; conspecificity ; data collection ; Density ; Density dependence ; development ; Developmental plasticity ; equations ; genotype ; Genotypes ; Growing season ; Larva - growth & development ; Larva - physiology ; larvae ; life history ; metamorphosis ; Metamorphosis, Biological ; Overwintering ; paedomorphosis ; Phenotype ; Phenotypes ; Phenotypic plasticity ; Plastic properties ; Plasticity ; polyphenism ; Population Density ; Predictive control ; Reptiles & amphibians ; salamander ; Seasons ; Snowpack</subject><ispartof>The Journal of animal ecology, 2024-11, Vol.93 (11), p.1747-1757</ispartof><rights>2024 The Author(s). Journal of Animal Ecology © 2024 British Ecological Society.</rights><rights>Journal of Animal Ecology © 2024 British Ecological Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2897-b8db31282ccb7639368e2ad0ca6673c3df18174b63ce663080433d1045f9a5fa3</cites><orcidid>0000-0001-8279-6417 ; 0000-0002-0093-0529 ; 0000-0001-5322-3126</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%2F1365-2656.14187$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1365-2656.14187$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39340187$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kirk, Mark A.</creatorcontrib><creatorcontrib>Lackey, Alycia C. R.</creatorcontrib><creatorcontrib>Reider, Kelsey E.</creatorcontrib><creatorcontrib>Thomas, Scott A.</creatorcontrib><creatorcontrib>Whiteman, Howard H.</creatorcontrib><title>Climate mediates the trade‐offs associated with phenotypic plasticity in an amphibian polyphenism</title><title>The Journal of animal ecology</title><addtitle>J Anim Ecol</addtitle><description>Polyphenisms occur when phenotypic plasticity produces morphologically distinct phenotypes from the same genotype. Plasticity is maintained through fitness trade‐offs which are conferred to different phenotypes under specific environmental contexts. Predicting the impacts of contemporary climate change on phenotypic plasticity is critical for climate‐sensitive animals like amphibians, but elucidating the selective pressures maintaining polyphenisms requires a framework to control for all mechanistic drivers of plasticity.
Using a 32‐year dataset documenting the larval and adult histories of 717 Arizona tiger salamanders (Ambystoma mavortium nebulosum), we determined how annual variation in climate and density dependence explained the maintenance of two distinct morphs (terrestrial metamorph vs. aquatic paedomorph) in a high‐elevation polyphenism. The effects of climate and conspecific density on morph development were evaluated with piecewise structural equation models (SEM) to tease apart the direct and indirect pathways by which these two mechanisms affect phenotypic plasticity.
Climate had a direct effect on morph outcome whereby longer growing seasons favoured metamorphic outcomes. Also, climate had indirect effects on morph outcome as mediated through density‐dependent effects, such as long overwintering coldspells corresponding to high cannibal densities and light snowpacks corresponding to high larval densities, both of which promoted paedomorphic outcomes.
Both climate and density dependence serve as important proxies for growth and resource limitation, which are important underlying drivers of the phenotypic plasticity in animal polyphenisms. Our findings motivate new studies to determine how contemporary climate change will alter the selective pressures maintaining phenotypic plasticity and polyphenisms.
Our research provides important and novel insight into how climate change underlies the maintenance of phenotypic plasticity.</description><subject>Adaptation, Physiological</subject><subject>adults</subject><subject>Ambystoma</subject><subject>Ambystoma - genetics</subject><subject>Ambystoma - physiology</subject><subject>Ambystoma mavortium nebulosum</subject><subject>Amphibians</subject><subject>animal ecology</subject><subject>Animals</subject><subject>Annual variations</subject><subject>Arizona</subject><subject>Climate</subject><subject>Climate Change</subject><subject>Climate effects</subject><subject>Climate models</subject><subject>Climate prediction</subject><subject>conspecificity</subject><subject>data collection</subject><subject>Density</subject><subject>Density dependence</subject><subject>development</subject><subject>Developmental plasticity</subject><subject>equations</subject><subject>genotype</subject><subject>Genotypes</subject><subject>Growing season</subject><subject>Larva - growth & development</subject><subject>Larva - physiology</subject><subject>larvae</subject><subject>life history</subject><subject>metamorphosis</subject><subject>Metamorphosis, Biological</subject><subject>Overwintering</subject><subject>paedomorphosis</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Phenotypic plasticity</subject><subject>Plastic properties</subject><subject>Plasticity</subject><subject>polyphenism</subject><subject>Population Density</subject><subject>Predictive control</subject><subject>Reptiles & amphibians</subject><subject>salamander</subject><subject>Seasons</subject><subject>Snowpack</subject><issn>0021-8790</issn><issn>1365-2656</issn><issn>1365-2656</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctOxCAUhonR6HhZuzMkbtxUOT0t0KWZjLcY3eiaUEozmHZaSyemOx_BZ_RJpM44CzdKSA6Bjz9wPkKOgZ1DGBeAPI1invJzSECKLTLZ7GyTCWMxRFJkbI_se__CGBMxw12yhxkmLPATYqaVq3VvaW0LF6qn_dzSvtOF_Xz_aMrSU-19Y8azgr65fk7buV00_dA6Q9tK-94Z1w_ULagOs27nLndh1TbVMJLO14dkp9SVt0frekCer2ZP05vo_vH6dnp5H5lYZiLKZZEjxDI2Jhc8PJFLG-uCGc25QINFCRJEknM0lnNkkiWIBbAkLTOdlhoPyNkqt-2a16X1vaqdN7aq9MI2S68Q0gQEE1z-AwWWAaLEgJ7-Ql-aZbcIHwlUnECWIIdAXawo0zXed7ZUbRca2w0KmBpVqVGMGsWob1Xhxsk6d5mH5m_4HzcB4CvgzVV2-CtP3V0-zFbJXxBlniE</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>Kirk, Mark A.</creator><creator>Lackey, Alycia C. R.</creator><creator>Reider, Kelsey E.</creator><creator>Thomas, Scott A.</creator><creator>Whiteman, Howard H.</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>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0001-8279-6417</orcidid><orcidid>https://orcid.org/0000-0002-0093-0529</orcidid><orcidid>https://orcid.org/0000-0001-5322-3126</orcidid></search><sort><creationdate>202411</creationdate><title>Climate mediates the trade‐offs associated with phenotypic plasticity in an amphibian polyphenism</title><author>Kirk, Mark A. ; Lackey, Alycia C. R. ; Reider, Kelsey E. ; Thomas, Scott A. ; Whiteman, Howard H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2897-b8db31282ccb7639368e2ad0ca6673c3df18174b63ce663080433d1045f9a5fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adaptation, Physiological</topic><topic>adults</topic><topic>Ambystoma</topic><topic>Ambystoma - genetics</topic><topic>Ambystoma - physiology</topic><topic>Ambystoma mavortium nebulosum</topic><topic>Amphibians</topic><topic>animal ecology</topic><topic>Animals</topic><topic>Annual variations</topic><topic>Arizona</topic><topic>Climate</topic><topic>Climate Change</topic><topic>Climate effects</topic><topic>Climate models</topic><topic>Climate prediction</topic><topic>conspecificity</topic><topic>data collection</topic><topic>Density</topic><topic>Density dependence</topic><topic>development</topic><topic>Developmental plasticity</topic><topic>equations</topic><topic>genotype</topic><topic>Genotypes</topic><topic>Growing season</topic><topic>Larva - growth & development</topic><topic>Larva - physiology</topic><topic>larvae</topic><topic>life history</topic><topic>metamorphosis</topic><topic>Metamorphosis, Biological</topic><topic>Overwintering</topic><topic>paedomorphosis</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Phenotypic plasticity</topic><topic>Plastic properties</topic><topic>Plasticity</topic><topic>polyphenism</topic><topic>Population Density</topic><topic>Predictive control</topic><topic>Reptiles & amphibians</topic><topic>salamander</topic><topic>Seasons</topic><topic>Snowpack</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kirk, Mark A.</creatorcontrib><creatorcontrib>Lackey, Alycia C. R.</creatorcontrib><creatorcontrib>Reider, Kelsey E.</creatorcontrib><creatorcontrib>Thomas, Scott A.</creatorcontrib><creatorcontrib>Whiteman, Howard H.</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>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><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>The Journal of animal ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kirk, Mark A.</au><au>Lackey, Alycia C. R.</au><au>Reider, Kelsey E.</au><au>Thomas, Scott A.</au><au>Whiteman, Howard H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Climate mediates the trade‐offs associated with phenotypic plasticity in an amphibian polyphenism</atitle><jtitle>The Journal of animal ecology</jtitle><addtitle>J Anim Ecol</addtitle><date>2024-11</date><risdate>2024</risdate><volume>93</volume><issue>11</issue><spage>1747</spage><epage>1757</epage><pages>1747-1757</pages><issn>0021-8790</issn><issn>1365-2656</issn><eissn>1365-2656</eissn><abstract>Polyphenisms occur when phenotypic plasticity produces morphologically distinct phenotypes from the same genotype. Plasticity is maintained through fitness trade‐offs which are conferred to different phenotypes under specific environmental contexts. Predicting the impacts of contemporary climate change on phenotypic plasticity is critical for climate‐sensitive animals like amphibians, but elucidating the selective pressures maintaining polyphenisms requires a framework to control for all mechanistic drivers of plasticity.
Using a 32‐year dataset documenting the larval and adult histories of 717 Arizona tiger salamanders (Ambystoma mavortium nebulosum), we determined how annual variation in climate and density dependence explained the maintenance of two distinct morphs (terrestrial metamorph vs. aquatic paedomorph) in a high‐elevation polyphenism. The effects of climate and conspecific density on morph development were evaluated with piecewise structural equation models (SEM) to tease apart the direct and indirect pathways by which these two mechanisms affect phenotypic plasticity.
Climate had a direct effect on morph outcome whereby longer growing seasons favoured metamorphic outcomes. Also, climate had indirect effects on morph outcome as mediated through density‐dependent effects, such as long overwintering coldspells corresponding to high cannibal densities and light snowpacks corresponding to high larval densities, both of which promoted paedomorphic outcomes.
Both climate and density dependence serve as important proxies for growth and resource limitation, which are important underlying drivers of the phenotypic plasticity in animal polyphenisms. Our findings motivate new studies to determine how contemporary climate change will alter the selective pressures maintaining phenotypic plasticity and polyphenisms.
Our research provides important and novel insight into how climate change underlies the maintenance of phenotypic plasticity.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>39340187</pmid><doi>10.1111/1365-2656.14187</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-8279-6417</orcidid><orcidid>https://orcid.org/0000-0002-0093-0529</orcidid><orcidid>https://orcid.org/0000-0001-5322-3126</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-8790 |
ispartof | The Journal of animal ecology, 2024-11, Vol.93 (11), p.1747-1757 |
issn | 0021-8790 1365-2656 1365-2656 |
language | eng |
recordid | cdi_proquest_miscellaneous_3110913383 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Adaptation, Physiological adults Ambystoma Ambystoma - genetics Ambystoma - physiology Ambystoma mavortium nebulosum Amphibians animal ecology Animals Annual variations Arizona Climate Climate Change Climate effects Climate models Climate prediction conspecificity data collection Density Density dependence development Developmental plasticity equations genotype Genotypes Growing season Larva - growth & development Larva - physiology larvae life history metamorphosis Metamorphosis, Biological Overwintering paedomorphosis Phenotype Phenotypes Phenotypic plasticity Plastic properties Plasticity polyphenism Population Density Predictive control Reptiles & amphibians salamander Seasons Snowpack |
title | Climate mediates the trade‐offs associated with phenotypic plasticity in an amphibian polyphenism |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T13%3A36%3A24IST&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=Climate%20mediates%20the%20trade%E2%80%90offs%20associated%20with%20phenotypic%20plasticity%20in%20an%20amphibian%20polyphenism&rft.jtitle=The%20Journal%20of%20animal%20ecology&rft.au=Kirk,%20Mark%20A.&rft.date=2024-11&rft.volume=93&rft.issue=11&rft.spage=1747&rft.epage=1757&rft.pages=1747-1757&rft.issn=0021-8790&rft.eissn=1365-2656&rft_id=info:doi/10.1111/1365-2656.14187&rft_dat=%3Cproquest_cross%3E3154170768%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=3124194361&rft_id=info:pmid/39340187&rfr_iscdi=true |