Cargando…

An evolutionary explanation of female‐biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L.

Sexual size dimorphism (SSD) is caused by differences in selection pressures and life‐history trade‐offs faced by males and females. Proximate causes of SSD may involve sex‐specific mortality, energy acquisition, and energy expenditure for maintenance, reproductive tissues, and reproductive behavior...

Descripción completa

Detalles Bibliográficos
Autores principales: Mollet, Fabian M., Enberg, Katja, Boukal, David S., Rijnsdorp, Adriaan D., Dieckmann, Ulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9885137/
https://www.ncbi.nlm.nih.gov/pubmed/36733451
http://dx.doi.org/10.1002/ece3.8070
_version_ 1784879866707968000
author Mollet, Fabian M.
Enberg, Katja
Boukal, David S.
Rijnsdorp, Adriaan D.
Dieckmann, Ulf
author_facet Mollet, Fabian M.
Enberg, Katja
Boukal, David S.
Rijnsdorp, Adriaan D.
Dieckmann, Ulf
author_sort Mollet, Fabian M.
collection PubMed
description Sexual size dimorphism (SSD) is caused by differences in selection pressures and life‐history trade‐offs faced by males and females. Proximate causes of SSD may involve sex‐specific mortality, energy acquisition, and energy expenditure for maintenance, reproductive tissues, and reproductive behavior. Using a quantitative, individual‐based, eco‐genetic model parameterized for North Sea plaice, we explore the importance of these mechanisms for female‐biased SSD, under which males are smaller and reach sexual maturity earlier than females (common among fish, but also arising in arthropods and mammals). We consider two mechanisms potentially serving as ultimate causes: (a) Male investments in male reproductive behavior might evolve to detract energy resources that would otherwise be available for somatic growth, and (b) diminishing returns on male reproductive investments might evolve to reduce energy acquisition. In general, both of these can bring about smaller male body sizes. We report the following findings. First, higher investments in male reproductive behavior alone cannot explain the North Sea plaice SSD. This is because such higher reproductive investments require increased energy acquisition, which would cause a delay in maturation, leading to male‐biased SSD contrary to observations. When accounting for the observed differential (lower) male mortality, maturation is postponed even further, leading to even larger males. Second, diminishing returns on male reproductive investments alone can qualitatively account for the North Sea plaice SSD, even though the quantitative match is imperfect. Third, both mechanisms can be reconciled with, and thus provide a mechanistic basis for, the previously advanced Ghiselin–Reiss hypothesis, according to which smaller males will evolve if their reproductive success is dominated by scramble competition for fertilizing females, as males would consequently invest more in reproduction than growth, potentially implying lower survival rates, and thus relaxing male–male competition. Fourth, a good quantitative fit with the North Sea plaice SSD is achieved by combining both mechanisms while accounting for sex‐specific costs males incur during their spawning season. Fifth, evolution caused by fishing is likely to have modified the North Sea plaice SSD.
format Online
Article
Text
id pubmed-9885137
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-98851372023-02-01 An evolutionary explanation of female‐biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L. Mollet, Fabian M. Enberg, Katja Boukal, David S. Rijnsdorp, Adriaan D. Dieckmann, Ulf Ecol Evol Original Research Sexual size dimorphism (SSD) is caused by differences in selection pressures and life‐history trade‐offs faced by males and females. Proximate causes of SSD may involve sex‐specific mortality, energy acquisition, and energy expenditure for maintenance, reproductive tissues, and reproductive behavior. Using a quantitative, individual‐based, eco‐genetic model parameterized for North Sea plaice, we explore the importance of these mechanisms for female‐biased SSD, under which males are smaller and reach sexual maturity earlier than females (common among fish, but also arising in arthropods and mammals). We consider two mechanisms potentially serving as ultimate causes: (a) Male investments in male reproductive behavior might evolve to detract energy resources that would otherwise be available for somatic growth, and (b) diminishing returns on male reproductive investments might evolve to reduce energy acquisition. In general, both of these can bring about smaller male body sizes. We report the following findings. First, higher investments in male reproductive behavior alone cannot explain the North Sea plaice SSD. This is because such higher reproductive investments require increased energy acquisition, which would cause a delay in maturation, leading to male‐biased SSD contrary to observations. When accounting for the observed differential (lower) male mortality, maturation is postponed even further, leading to even larger males. Second, diminishing returns on male reproductive investments alone can qualitatively account for the North Sea plaice SSD, even though the quantitative match is imperfect. Third, both mechanisms can be reconciled with, and thus provide a mechanistic basis for, the previously advanced Ghiselin–Reiss hypothesis, according to which smaller males will evolve if their reproductive success is dominated by scramble competition for fertilizing females, as males would consequently invest more in reproduction than growth, potentially implying lower survival rates, and thus relaxing male–male competition. Fourth, a good quantitative fit with the North Sea plaice SSD is achieved by combining both mechanisms while accounting for sex‐specific costs males incur during their spawning season. Fifth, evolution caused by fishing is likely to have modified the North Sea plaice SSD. John Wiley and Sons Inc. 2023-01-30 /pmc/articles/PMC9885137/ /pubmed/36733451 http://dx.doi.org/10.1002/ece3.8070 Text en © 2023 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Mollet, Fabian M.
Enberg, Katja
Boukal, David S.
Rijnsdorp, Adriaan D.
Dieckmann, Ulf
An evolutionary explanation of female‐biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L.
title An evolutionary explanation of female‐biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L.
title_full An evolutionary explanation of female‐biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L.
title_fullStr An evolutionary explanation of female‐biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L.
title_full_unstemmed An evolutionary explanation of female‐biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L.
title_short An evolutionary explanation of female‐biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L.
title_sort evolutionary explanation of female‐biased sexual size dimorphism in north sea plaice, pleuronectes platessa l.
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9885137/
https://www.ncbi.nlm.nih.gov/pubmed/36733451
http://dx.doi.org/10.1002/ece3.8070
work_keys_str_mv AT molletfabianm anevolutionaryexplanationoffemalebiasedsexualsizedimorphisminnorthseaplaicepleuronectesplatessal
AT enbergkatja anevolutionaryexplanationoffemalebiasedsexualsizedimorphisminnorthseaplaicepleuronectesplatessal
AT boukaldavids anevolutionaryexplanationoffemalebiasedsexualsizedimorphisminnorthseaplaicepleuronectesplatessal
AT rijnsdorpadriaand anevolutionaryexplanationoffemalebiasedsexualsizedimorphisminnorthseaplaicepleuronectesplatessal
AT dieckmannulf anevolutionaryexplanationoffemalebiasedsexualsizedimorphisminnorthseaplaicepleuronectesplatessal
AT molletfabianm evolutionaryexplanationoffemalebiasedsexualsizedimorphisminnorthseaplaicepleuronectesplatessal
AT enbergkatja evolutionaryexplanationoffemalebiasedsexualsizedimorphisminnorthseaplaicepleuronectesplatessal
AT boukaldavids evolutionaryexplanationoffemalebiasedsexualsizedimorphisminnorthseaplaicepleuronectesplatessal
AT rijnsdorpadriaand evolutionaryexplanationoffemalebiasedsexualsizedimorphisminnorthseaplaicepleuronectesplatessal
AT dieckmannulf evolutionaryexplanationoffemalebiasedsexualsizedimorphisminnorthseaplaicepleuronectesplatessal