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Nutrient‐dependent allometric plasticity in a male‐diphenic mite

Male secondary sexual traits often scale allometrically with body size. These allometries can be variable within species and may shift depending on environmental conditions, such as food quality. Such allometric plasticity has been hypothesized to initiate local adaptation and evolutionary diversifi...

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Autores principales: Rhebergen, Flor T., Stewart, Kathryn A., Smallegange, Isabel M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343935/
https://www.ncbi.nlm.nih.gov/pubmed/35928796
http://dx.doi.org/10.1002/ece3.9145
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author Rhebergen, Flor T.
Stewart, Kathryn A.
Smallegange, Isabel M.
author_facet Rhebergen, Flor T.
Stewart, Kathryn A.
Smallegange, Isabel M.
author_sort Rhebergen, Flor T.
collection PubMed
description Male secondary sexual traits often scale allometrically with body size. These allometries can be variable within species and may shift depending on environmental conditions, such as food quality. Such allometric plasticity has been hypothesized to initiate local adaptation and evolutionary diversification of scaling relationships, but is under‐recorded, and its eco‐evolutionary effects are not well understood. Here, we tested for allometric plasticity in the bulb mite (Rhizoglyphus robini), in which large males tend to develop as armed adult fighters with thickened third legs, while small males become adult scramblers without thickened legs. We first examined the ontogenetic timing for size‐ and growth‐dependent male morph determination, using experimentally amplified fluctuations in growth rate throughout juvenile development. Having established that somatic growth and body size determine male morph expression immediately before metamorphosis, we examined whether the relationship between adult male morph and size at metamorphosis shifts with food quality. We found that the threshold body size for male morph expression shifts toward lower values with deteriorating food quality, confirming food‐dependent allometric plasticity. Such allometric plasticity may allow populations to track prevailing nutritional conditions, potentially facilitating rapid evolution of allometric scaling relationships.
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spelling pubmed-93439352022-08-03 Nutrient‐dependent allometric plasticity in a male‐diphenic mite Rhebergen, Flor T. Stewart, Kathryn A. Smallegange, Isabel M. Ecol Evol Research Articles Male secondary sexual traits often scale allometrically with body size. These allometries can be variable within species and may shift depending on environmental conditions, such as food quality. Such allometric plasticity has been hypothesized to initiate local adaptation and evolutionary diversification of scaling relationships, but is under‐recorded, and its eco‐evolutionary effects are not well understood. Here, we tested for allometric plasticity in the bulb mite (Rhizoglyphus robini), in which large males tend to develop as armed adult fighters with thickened third legs, while small males become adult scramblers without thickened legs. We first examined the ontogenetic timing for size‐ and growth‐dependent male morph determination, using experimentally amplified fluctuations in growth rate throughout juvenile development. Having established that somatic growth and body size determine male morph expression immediately before metamorphosis, we examined whether the relationship between adult male morph and size at metamorphosis shifts with food quality. We found that the threshold body size for male morph expression shifts toward lower values with deteriorating food quality, confirming food‐dependent allometric plasticity. Such allometric plasticity may allow populations to track prevailing nutritional conditions, potentially facilitating rapid evolution of allometric scaling relationships. John Wiley and Sons Inc. 2022-08-01 /pmc/articles/PMC9343935/ /pubmed/35928796 http://dx.doi.org/10.1002/ece3.9145 Text en © 2022 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 Research Articles
Rhebergen, Flor T.
Stewart, Kathryn A.
Smallegange, Isabel M.
Nutrient‐dependent allometric plasticity in a male‐diphenic mite
title Nutrient‐dependent allometric plasticity in a male‐diphenic mite
title_full Nutrient‐dependent allometric plasticity in a male‐diphenic mite
title_fullStr Nutrient‐dependent allometric plasticity in a male‐diphenic mite
title_full_unstemmed Nutrient‐dependent allometric plasticity in a male‐diphenic mite
title_short Nutrient‐dependent allometric plasticity in a male‐diphenic mite
title_sort nutrient‐dependent allometric plasticity in a male‐diphenic mite
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343935/
https://www.ncbi.nlm.nih.gov/pubmed/35928796
http://dx.doi.org/10.1002/ece3.9145
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