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Male-driven reproductive and agonistic character displacement in darters and its implications for speciation in allopatry
Selection against hybridization can cause mating traits to diverge between species in sympatry via reproductive character displacement (RCD). Additionally, selection against interspecific fighting can cause aggressive traits to diverge between sympatric species via agonistic character displacement (...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809036/ https://www.ncbi.nlm.nih.gov/pubmed/29492043 http://dx.doi.org/10.1093/cz/zox069 |
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author | Moran, Rachel L Fuller, Rebecca C |
author_facet | Moran, Rachel L Fuller, Rebecca C |
author_sort | Moran, Rachel L |
collection | PubMed |
description | Selection against hybridization can cause mating traits to diverge between species in sympatry via reproductive character displacement (RCD). Additionally, selection against interspecific fighting can cause aggressive traits to diverge between sympatric species via agonistic character displacement (ACD). By directly affecting conspecific recognition traits, RCD and ACD between species can also incidentally cause divergence in mating and fighting traits among populations within a species [termed cascade RCD (CRCD) and cascade ACD]. Here, we demonstrate patterns consistent with male-driven RCD and ACD in 2 groups of darters (orangethroat darter clade Ceasia and rainbow darter Etheostoma caeruleum). In both groups, males that occur in sympatry (between Ceasia and E. caeruleum) have higher levels of preference for mating and fighting with conspecifics over heterospecifics than do males from allopatry. This is consistent with RCD and ACD. We also found patterns consistent with CRCD and cascade ACD among species of Ceasia. Ceasia males that are sympatric to E. caeruleum (but allopatric to one another) also have heightened preferences for mating and fighting with conspecific versus heterospecific Ceasia. In contrast, Ceasia males that are allopatric to E. caeruleum readily mate and fight with heterospecific Ceasia. We suggest that RCD and ACD between Ceasia and E. caeruleum has incidentally led to divergence in mating and fighting traits among Ceasia species. This study is unique in that male preferences evolve via both RCD (male preference for conspecific females) and ACD (male preference to fight conspecific males) which leads to subsequent divergence among allopatric lineages. |
format | Online Article Text |
id | pubmed-5809036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58090362018-02-28 Male-driven reproductive and agonistic character displacement in darters and its implications for speciation in allopatry Moran, Rachel L Fuller, Rebecca C Curr Zool Special Column: Male Competition and Speciation Selection against hybridization can cause mating traits to diverge between species in sympatry via reproductive character displacement (RCD). Additionally, selection against interspecific fighting can cause aggressive traits to diverge between sympatric species via agonistic character displacement (ACD). By directly affecting conspecific recognition traits, RCD and ACD between species can also incidentally cause divergence in mating and fighting traits among populations within a species [termed cascade RCD (CRCD) and cascade ACD]. Here, we demonstrate patterns consistent with male-driven RCD and ACD in 2 groups of darters (orangethroat darter clade Ceasia and rainbow darter Etheostoma caeruleum). In both groups, males that occur in sympatry (between Ceasia and E. caeruleum) have higher levels of preference for mating and fighting with conspecifics over heterospecifics than do males from allopatry. This is consistent with RCD and ACD. We also found patterns consistent with CRCD and cascade ACD among species of Ceasia. Ceasia males that are sympatric to E. caeruleum (but allopatric to one another) also have heightened preferences for mating and fighting with conspecific versus heterospecific Ceasia. In contrast, Ceasia males that are allopatric to E. caeruleum readily mate and fight with heterospecific Ceasia. We suggest that RCD and ACD between Ceasia and E. caeruleum has incidentally led to divergence in mating and fighting traits among Ceasia species. This study is unique in that male preferences evolve via both RCD (male preference for conspecific females) and ACD (male preference to fight conspecific males) which leads to subsequent divergence among allopatric lineages. Oxford University Press 2018-02 2017-11-27 /pmc/articles/PMC5809036/ /pubmed/29492043 http://dx.doi.org/10.1093/cz/zox069 Text en © The Author (2017). Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Special Column: Male Competition and Speciation Moran, Rachel L Fuller, Rebecca C Male-driven reproductive and agonistic character displacement in darters and its implications for speciation in allopatry |
title | Male-driven reproductive and agonistic character displacement in darters and its implications for speciation in allopatry |
title_full | Male-driven reproductive and agonistic character displacement in darters and its implications for speciation in allopatry |
title_fullStr | Male-driven reproductive and agonistic character displacement in darters and its implications for speciation in allopatry |
title_full_unstemmed | Male-driven reproductive and agonistic character displacement in darters and its implications for speciation in allopatry |
title_short | Male-driven reproductive and agonistic character displacement in darters and its implications for speciation in allopatry |
title_sort | male-driven reproductive and agonistic character displacement in darters and its implications for speciation in allopatry |
topic | Special Column: Male Competition and Speciation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809036/ https://www.ncbi.nlm.nih.gov/pubmed/29492043 http://dx.doi.org/10.1093/cz/zox069 |
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