Loading…

An eco‐evolutionary feedback loop between population dynamics and fighter expression affects the evolution of alternative reproductive tactics

Surprisingly, little is known about how eco‐evolutionary feedback loops affect trait dynamics within a single population. Polymorphisms of discrete alternative phenotypes present ideal test beds to investigate this, as the alternative phenotypes typically exhibit contrasting demographic rates mediat...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of animal ecology 2019-01, Vol.88 (1), p.11-23
Main Authors: Croll, Jasper C., Egas, Martijn, Smallegange, Isabel M., Bassar, Ron
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c4689-a08d02dcf79e3b11613c570af372ef27311ad2c81fb7a08967a98cdf35c87c683
cites cdi_FETCH-LOGICAL-c4689-a08d02dcf79e3b11613c570af372ef27311ad2c81fb7a08967a98cdf35c87c683
container_end_page 23
container_issue 1
container_start_page 11
container_title The Journal of animal ecology
container_volume 88
creator Croll, Jasper C.
Egas, Martijn
Smallegange, Isabel M.
Bassar, Ron
description Surprisingly, little is known about how eco‐evolutionary feedback loops affect trait dynamics within a single population. Polymorphisms of discrete alternative phenotypes present ideal test beds to investigate this, as the alternative phenotypes typically exhibit contrasting demographic rates mediated through frequency or density dependence, and are thus differentially affected by selection. Alternative reproductive tactics (ARTs), like male fighters and sneakers, are an extreme form of discrete phenotype expression and occur across many taxa. Fighters possess weapons for male–male competition over access to mates, whereas sneakers are defenceless but adopt tactics like female‐mimicking. Because fighters in some species mortally injure conspecifics, this raises the question whether fighter expression can feed back to affect population size and structure, thereby altering the selection gradient and evolutionary dynamics of ART expression in an eco‐evolutionary feedback loop. Here, we investigated how the eco‐evolutionary feedback loop between fighter expression and population size and structure affects the evolution and maintenance of ARTs. We introduced intraspecific killing by fighters in a two‐sex, two‐ART population model parameterized for the male dimorphic bulb mite (Rhizoglyphus robini) that includes life‐history differences between the ARTs and a mating‐probability matrix analogous to the classic hawk–dove game. Using adaptive dynamics, we found that the intraspecific killing by fighters can extend the range of life‐history parameter values under which ARTs evolve, because fighters that kill other fighters decrease fighter fitness. This effect can be nullified when benefits from killing are incorporated, like increased reproduction through increased energy uptake. The eco‐evolutionary feedback effects found here for a dimorphic trait likely also occur in other fitness‐related traits, such as behavioural syndromes, parental care and niche construction traits. Current theoretical advances to model eco‐evolutionary processes, and empirical steps towards unravelling the underlying drivers, pave the way for understanding how selection affects trait evolution in an eco‐evolutionary feedback loop. Life cycle links between killing and copulating highlight the importance of studying eco‐evolutionary interactions. Using a theoretical model, the authors show how the intraspecific killing of conspecifics affects the ecological dynamics of a population, which fe
doi_str_mv 10.1111/1365-2656.12899
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7380021</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2091232285</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4689-a08d02dcf79e3b11613c570af372ef27311ad2c81fb7a08967a98cdf35c87c683</originalsourceid><addsrcrecordid>eNqFkbtuFDEUhi0EIkugpkOWaNJM4gvjS4O0igIkikIDteXxHGcneMeDPbNhOx4hz8iT4MmGFaTBzZF9Pn-yz4_Qa0qOaVknlIu6YqIWx5QprZ-gxf7kKVoQwmilpCYH6EXON4QQyQh_jg44oazmgizQ3bLH4OKvn3ewiWEau9jbtMUeoG2s-4ZDjANuYLwF6PEQhynYmcHttrfrzmVs-xb77no1QsLwY0iQ89y33oMbMx5XgPdmHD22oZB9kWwAJxhSbCd3vxltqS6_RM-8DRlePdRD9PXD2ZfTT9Xl54_np8vLyr0TSleWqJaw1nmpgTeUCspdLYn1XDLwTHJKbcucor6RhdVCWq1c63ntlHRC8UP0fucdpmYNrYN-TDaYIXXrMgATbWf-7fTdylzHjZFczXMtgqMHQYrfJ8ijWXfZQQi2hzhlw4imjDOm6oK-fYTexKkMIRSKCqWUplwX6mRHuRRzTuD3j6HEzGmbOVszZ2vu0y433vz9hz3_J94CiB1w2wXY_s9nLpZXZzvzb13aufU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2168889139</pqid></control><display><type>article</type><title>An eco‐evolutionary feedback loop between population dynamics and fighter expression affects the evolution of alternative reproductive tactics</title><source>Wiley</source><creator>Croll, Jasper C. ; Egas, Martijn ; Smallegange, Isabel M. ; Bassar, Ron</creator><contributor>Bassar, Ron</contributor><creatorcontrib>Croll, Jasper C. ; Egas, Martijn ; Smallegange, Isabel M. ; Bassar, Ron ; Bassar, Ron</creatorcontrib><description>Surprisingly, little is known about how eco‐evolutionary feedback loops affect trait dynamics within a single population. Polymorphisms of discrete alternative phenotypes present ideal test beds to investigate this, as the alternative phenotypes typically exhibit contrasting demographic rates mediated through frequency or density dependence, and are thus differentially affected by selection. Alternative reproductive tactics (ARTs), like male fighters and sneakers, are an extreme form of discrete phenotype expression and occur across many taxa. Fighters possess weapons for male–male competition over access to mates, whereas sneakers are defenceless but adopt tactics like female‐mimicking. Because fighters in some species mortally injure conspecifics, this raises the question whether fighter expression can feed back to affect population size and structure, thereby altering the selection gradient and evolutionary dynamics of ART expression in an eco‐evolutionary feedback loop. Here, we investigated how the eco‐evolutionary feedback loop between fighter expression and population size and structure affects the evolution and maintenance of ARTs. We introduced intraspecific killing by fighters in a two‐sex, two‐ART population model parameterized for the male dimorphic bulb mite (Rhizoglyphus robini) that includes life‐history differences between the ARTs and a mating‐probability matrix analogous to the classic hawk–dove game. Using adaptive dynamics, we found that the intraspecific killing by fighters can extend the range of life‐history parameter values under which ARTs evolve, because fighters that kill other fighters decrease fighter fitness. This effect can be nullified when benefits from killing are incorporated, like increased reproduction through increased energy uptake. The eco‐evolutionary feedback effects found here for a dimorphic trait likely also occur in other fitness‐related traits, such as behavioural syndromes, parental care and niche construction traits. Current theoretical advances to model eco‐evolutionary processes, and empirical steps towards unravelling the underlying drivers, pave the way for understanding how selection affects trait evolution in an eco‐evolutionary feedback loop. Life cycle links between killing and copulating highlight the importance of studying eco‐evolutionary interactions. Using a theoretical model, the authors show how the intraspecific killing of conspecifics affects the ecological dynamics of a population, which feeds back to influence the evolution of what reproductive strategies males employ to gain access to females.</description><identifier>ISSN: 0021-8790</identifier><identifier>EISSN: 1365-2656</identifier><identifier>DOI: 10.1111/1365-2656.12899</identifier><identifier>PMID: 30125360</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>adaptive dynamics ; alternative reproductive phenotype ; cannibalism ; coexistence ; Conspecifics ; Demographics ; Density dependence ; Dependence ; Dynamics ; Eco‐evolutionary Dynamics across Scales ; environmental threshold model ; Evolution ; Feedback ; Feedback loops ; Fitness ; Mimicry ; Phenotypes ; Population ; population dynamics ; Population number ; Reproductive fitness ; Tactics</subject><ispartof>The Journal of animal ecology, 2019-01, Vol.88 (1), p.11-23</ispartof><rights>2018 The Authors. published by John Wiley &amp; Sons Ltd on behalf of British Ecological Society.</rights><rights>2018 The Authors. Journal of Animal Ecology published by John Wiley &amp; Sons Ltd on behalf of British Ecological Society.</rights><rights>Journal of Animal Ecology © 2019 British Ecological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4689-a08d02dcf79e3b11613c570af372ef27311ad2c81fb7a08967a98cdf35c87c683</citedby><cites>FETCH-LOGICAL-c4689-a08d02dcf79e3b11613c570af372ef27311ad2c81fb7a08967a98cdf35c87c683</cites><orcidid>0000-0001-6218-7358</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30125360$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Bassar, Ron</contributor><creatorcontrib>Croll, Jasper C.</creatorcontrib><creatorcontrib>Egas, Martijn</creatorcontrib><creatorcontrib>Smallegange, Isabel M.</creatorcontrib><creatorcontrib>Bassar, Ron</creatorcontrib><title>An eco‐evolutionary feedback loop between population dynamics and fighter expression affects the evolution of alternative reproductive tactics</title><title>The Journal of animal ecology</title><addtitle>J Anim Ecol</addtitle><description>Surprisingly, little is known about how eco‐evolutionary feedback loops affect trait dynamics within a single population. Polymorphisms of discrete alternative phenotypes present ideal test beds to investigate this, as the alternative phenotypes typically exhibit contrasting demographic rates mediated through frequency or density dependence, and are thus differentially affected by selection. Alternative reproductive tactics (ARTs), like male fighters and sneakers, are an extreme form of discrete phenotype expression and occur across many taxa. Fighters possess weapons for male–male competition over access to mates, whereas sneakers are defenceless but adopt tactics like female‐mimicking. Because fighters in some species mortally injure conspecifics, this raises the question whether fighter expression can feed back to affect population size and structure, thereby altering the selection gradient and evolutionary dynamics of ART expression in an eco‐evolutionary feedback loop. Here, we investigated how the eco‐evolutionary feedback loop between fighter expression and population size and structure affects the evolution and maintenance of ARTs. We introduced intraspecific killing by fighters in a two‐sex, two‐ART population model parameterized for the male dimorphic bulb mite (Rhizoglyphus robini) that includes life‐history differences between the ARTs and a mating‐probability matrix analogous to the classic hawk–dove game. Using adaptive dynamics, we found that the intraspecific killing by fighters can extend the range of life‐history parameter values under which ARTs evolve, because fighters that kill other fighters decrease fighter fitness. This effect can be nullified when benefits from killing are incorporated, like increased reproduction through increased energy uptake. The eco‐evolutionary feedback effects found here for a dimorphic trait likely also occur in other fitness‐related traits, such as behavioural syndromes, parental care and niche construction traits. Current theoretical advances to model eco‐evolutionary processes, and empirical steps towards unravelling the underlying drivers, pave the way for understanding how selection affects trait evolution in an eco‐evolutionary feedback loop. Life cycle links between killing and copulating highlight the importance of studying eco‐evolutionary interactions. Using a theoretical model, the authors show how the intraspecific killing of conspecifics affects the ecological dynamics of a population, which feeds back to influence the evolution of what reproductive strategies males employ to gain access to females.</description><subject>adaptive dynamics</subject><subject>alternative reproductive phenotype</subject><subject>cannibalism</subject><subject>coexistence</subject><subject>Conspecifics</subject><subject>Demographics</subject><subject>Density dependence</subject><subject>Dependence</subject><subject>Dynamics</subject><subject>Eco‐evolutionary Dynamics across Scales</subject><subject>environmental threshold model</subject><subject>Evolution</subject><subject>Feedback</subject><subject>Feedback loops</subject><subject>Fitness</subject><subject>Mimicry</subject><subject>Phenotypes</subject><subject>Population</subject><subject>population dynamics</subject><subject>Population number</subject><subject>Reproductive fitness</subject><subject>Tactics</subject><issn>0021-8790</issn><issn>1365-2656</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkbtuFDEUhi0EIkugpkOWaNJM4gvjS4O0igIkikIDteXxHGcneMeDPbNhOx4hz8iT4MmGFaTBzZF9Pn-yz4_Qa0qOaVknlIu6YqIWx5QprZ-gxf7kKVoQwmilpCYH6EXON4QQyQh_jg44oazmgizQ3bLH4OKvn3ewiWEau9jbtMUeoG2s-4ZDjANuYLwF6PEQhynYmcHttrfrzmVs-xb77no1QsLwY0iQ89y33oMbMx5XgPdmHD22oZB9kWwAJxhSbCd3vxltqS6_RM-8DRlePdRD9PXD2ZfTT9Xl54_np8vLyr0TSleWqJaw1nmpgTeUCspdLYn1XDLwTHJKbcucor6RhdVCWq1c63ntlHRC8UP0fucdpmYNrYN-TDaYIXXrMgATbWf-7fTdylzHjZFczXMtgqMHQYrfJ8ijWXfZQQi2hzhlw4imjDOm6oK-fYTexKkMIRSKCqWUplwX6mRHuRRzTuD3j6HEzGmbOVszZ2vu0y433vz9hz3_J94CiB1w2wXY_s9nLpZXZzvzb13aufU</recordid><startdate>201901</startdate><enddate>201901</enddate><creator>Croll, Jasper C.</creator><creator>Egas, Martijn</creator><creator>Smallegange, Isabel M.</creator><creator>Bassar, Ron</creator><general>Blackwell Publishing Ltd</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</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>5PM</scope><orcidid>https://orcid.org/0000-0001-6218-7358</orcidid></search><sort><creationdate>201901</creationdate><title>An eco‐evolutionary feedback loop between population dynamics and fighter expression affects the evolution of alternative reproductive tactics</title><author>Croll, Jasper C. ; Egas, Martijn ; Smallegange, Isabel M. ; Bassar, Ron</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4689-a08d02dcf79e3b11613c570af372ef27311ad2c81fb7a08967a98cdf35c87c683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>adaptive dynamics</topic><topic>alternative reproductive phenotype</topic><topic>cannibalism</topic><topic>coexistence</topic><topic>Conspecifics</topic><topic>Demographics</topic><topic>Density dependence</topic><topic>Dependence</topic><topic>Dynamics</topic><topic>Eco‐evolutionary Dynamics across Scales</topic><topic>environmental threshold model</topic><topic>Evolution</topic><topic>Feedback</topic><topic>Feedback loops</topic><topic>Fitness</topic><topic>Mimicry</topic><topic>Phenotypes</topic><topic>Population</topic><topic>population dynamics</topic><topic>Population number</topic><topic>Reproductive fitness</topic><topic>Tactics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Croll, Jasper C.</creatorcontrib><creatorcontrib>Egas, Martijn</creatorcontrib><creatorcontrib>Smallegange, Isabel M.</creatorcontrib><creatorcontrib>Bassar, Ron</creatorcontrib><collection>Open Access: Wiley-Blackwell Open Access Journals</collection><collection>Wiley Online Library Free Content</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>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of animal ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Croll, Jasper C.</au><au>Egas, Martijn</au><au>Smallegange, Isabel M.</au><au>Bassar, Ron</au><au>Bassar, Ron</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An eco‐evolutionary feedback loop between population dynamics and fighter expression affects the evolution of alternative reproductive tactics</atitle><jtitle>The Journal of animal ecology</jtitle><addtitle>J Anim Ecol</addtitle><date>2019-01</date><risdate>2019</risdate><volume>88</volume><issue>1</issue><spage>11</spage><epage>23</epage><pages>11-23</pages><issn>0021-8790</issn><eissn>1365-2656</eissn><abstract>Surprisingly, little is known about how eco‐evolutionary feedback loops affect trait dynamics within a single population. Polymorphisms of discrete alternative phenotypes present ideal test beds to investigate this, as the alternative phenotypes typically exhibit contrasting demographic rates mediated through frequency or density dependence, and are thus differentially affected by selection. Alternative reproductive tactics (ARTs), like male fighters and sneakers, are an extreme form of discrete phenotype expression and occur across many taxa. Fighters possess weapons for male–male competition over access to mates, whereas sneakers are defenceless but adopt tactics like female‐mimicking. Because fighters in some species mortally injure conspecifics, this raises the question whether fighter expression can feed back to affect population size and structure, thereby altering the selection gradient and evolutionary dynamics of ART expression in an eco‐evolutionary feedback loop. Here, we investigated how the eco‐evolutionary feedback loop between fighter expression and population size and structure affects the evolution and maintenance of ARTs. We introduced intraspecific killing by fighters in a two‐sex, two‐ART population model parameterized for the male dimorphic bulb mite (Rhizoglyphus robini) that includes life‐history differences between the ARTs and a mating‐probability matrix analogous to the classic hawk–dove game. Using adaptive dynamics, we found that the intraspecific killing by fighters can extend the range of life‐history parameter values under which ARTs evolve, because fighters that kill other fighters decrease fighter fitness. This effect can be nullified when benefits from killing are incorporated, like increased reproduction through increased energy uptake. The eco‐evolutionary feedback effects found here for a dimorphic trait likely also occur in other fitness‐related traits, such as behavioural syndromes, parental care and niche construction traits. Current theoretical advances to model eco‐evolutionary processes, and empirical steps towards unravelling the underlying drivers, pave the way for understanding how selection affects trait evolution in an eco‐evolutionary feedback loop. Life cycle links between killing and copulating highlight the importance of studying eco‐evolutionary interactions. Using a theoretical model, the authors show how the intraspecific killing of conspecifics affects the ecological dynamics of a population, which feeds back to influence the evolution of what reproductive strategies males employ to gain access to females.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>30125360</pmid><doi>10.1111/1365-2656.12899</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-6218-7358</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-8790
ispartof The Journal of animal ecology, 2019-01, Vol.88 (1), p.11-23
issn 0021-8790
1365-2656
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7380021
source Wiley
subjects adaptive dynamics
alternative reproductive phenotype
cannibalism
coexistence
Conspecifics
Demographics
Density dependence
Dependence
Dynamics
Eco‐evolutionary Dynamics across Scales
environmental threshold model
Evolution
Feedback
Feedback loops
Fitness
Mimicry
Phenotypes
Population
population dynamics
Population number
Reproductive fitness
Tactics
title An eco‐evolutionary feedback loop between population dynamics and fighter expression affects the evolution of alternative reproductive tactics
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T03%3A40%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=An%20eco%E2%80%90evolutionary%20feedback%20loop%20between%20population%20dynamics%20and%20fighter%20expression%20affects%20the%20evolution%20of%20alternative%20reproductive%20tactics&rft.jtitle=The%20Journal%20of%20animal%20ecology&rft.au=Croll,%20Jasper%20C.&rft.date=2019-01&rft.volume=88&rft.issue=1&rft.spage=11&rft.epage=23&rft.pages=11-23&rft.issn=0021-8790&rft.eissn=1365-2656&rft_id=info:doi/10.1111/1365-2656.12899&rft_dat=%3Cproquest_pubme%3E2091232285%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4689-a08d02dcf79e3b11613c570af372ef27311ad2c81fb7a08967a98cdf35c87c683%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2168889139&rft_id=info:pmid/30125360&rfr_iscdi=true