<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lerch BA</submitter><funding>National Science Foundation</funding><pagination>e3002059</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10101644</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(4)</volume><pubmed_abstract>Predation plays a role in preventing the evolution of ever more complicated sexual displays, because such displays often increase an individual's predation risk. Sexual selection theory, however, omits a key feature of predation in modeling costs to sexually selected traits: Predation is density dependent. As a result of this density dependence, predator-prey dynamics should feed back into the evolution of sexual displays, which, in turn, feeds back into predator-prey dynamics. Here, we develop both population and quantitative genetic models of sexual selection that explicitly link the evolution of sexual displays with predator-prey dynamics. Our primary result is that predation can drive eco-evolutionary cycles in sexually selected traits. We also show that mechanistically modeling the co</pubmed_abstract><journal>PLoS biology</journal><pubmed_title>Predation drives complex eco-evolutionary dynamics in sexually selected traits.</pubmed_title><pmcid>PMC10101644</pmcid><funding_grant_id>DEB-1939290</funding_grant_id><pubmed_authors>Servedio MR</pubmed_authors><pubmed_authors>Lerch BA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Predation drives complex eco-evolutionary dynamics in sexually selected traits.</name><description>Predation plays a role in preventing the evolution of ever more complicated sexual displays, because such displays often increase an individual's predation risk. Sexual selection theory, however, omits a key feature of predation in modeling costs to sexually selected traits: Predation is density dependent. As a result of this density dependence, predator-prey dynamics should feed back into the evolution of sexual displays, which, in turn, feeds back into predator-prey dynamics. Here, we develop both population and quantitative genetic models of sexual selection that explicitly link the evolution of sexual displays with predator-prey dynamics. Our primary result is that predation can drive eco-evolutionary cycles in sexually selected traits. We also show that mechanistically modeling the co</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-19T23:48:30.809Z</modification><creation>2025-04-19T23:48:30.809Z</creation></dates><accession>S-EPMC10101644</accession><cross_references><pubmed>37011094</pubmed><doi>10.1371/journal.pbio.3002059</doi></cross_references></HashMap>