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Anomalous invasion dynamics due to dispersal polymorphism and dispersal–reproduction trade-offs

Dispersal polymorphism and mutation play significant roles during biological invasions, potentially leading to evolution and complex behaviour such as accelerating or decelerating invasion fronts. However, life-history theory predicts that reproductive fitness—another key determinant of invasion dyn...

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Detalles Bibliográficos
Autores principales: Keenan, Vincent A., Cornell, Stephen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7892423/
https://www.ncbi.nlm.nih.gov/pubmed/33434455
http://dx.doi.org/10.1098/rspb.2020.2825
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author Keenan, Vincent A.
Cornell, Stephen J.
author_facet Keenan, Vincent A.
Cornell, Stephen J.
author_sort Keenan, Vincent A.
collection PubMed
description Dispersal polymorphism and mutation play significant roles during biological invasions, potentially leading to evolution and complex behaviour such as accelerating or decelerating invasion fronts. However, life-history theory predicts that reproductive fitness—another key determinant of invasion dynamics—may be lower for more dispersive strains. Here, we use a mathematical model to show that unexpected invasion dynamics emerge from the combination of heritable dispersal polymorphism, dispersal-fitness trade-offs, and mutation between strains. We show that the invasion dynamics are determined by the trade-off relationship between dispersal and population growth rates of the constituent strains. We find that invasion dynamics can be ‘anomalous’ (i.e. faster than any of the strains in isolation), but that the ultimate invasion speed is determined by the traits of, at most, two strains. The model is simple but generic, so we expect the predictions to apply to a wide range of ecological, evolutionary, or epidemiological invasions.
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spelling pubmed-78924232021-02-27 Anomalous invasion dynamics due to dispersal polymorphism and dispersal–reproduction trade-offs Keenan, Vincent A. Cornell, Stephen J. Proc Biol Sci Ecology Dispersal polymorphism and mutation play significant roles during biological invasions, potentially leading to evolution and complex behaviour such as accelerating or decelerating invasion fronts. However, life-history theory predicts that reproductive fitness—another key determinant of invasion dynamics—may be lower for more dispersive strains. Here, we use a mathematical model to show that unexpected invasion dynamics emerge from the combination of heritable dispersal polymorphism, dispersal-fitness trade-offs, and mutation between strains. We show that the invasion dynamics are determined by the trade-off relationship between dispersal and population growth rates of the constituent strains. We find that invasion dynamics can be ‘anomalous’ (i.e. faster than any of the strains in isolation), but that the ultimate invasion speed is determined by the traits of, at most, two strains. The model is simple but generic, so we expect the predictions to apply to a wide range of ecological, evolutionary, or epidemiological invasions. The Royal Society 2021-01-13 2021-01-13 /pmc/articles/PMC7892423/ /pubmed/33434455 http://dx.doi.org/10.1098/rspb.2020.2825 Text en © 2021 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Ecology
Keenan, Vincent A.
Cornell, Stephen J.
Anomalous invasion dynamics due to dispersal polymorphism and dispersal–reproduction trade-offs
title Anomalous invasion dynamics due to dispersal polymorphism and dispersal–reproduction trade-offs
title_full Anomalous invasion dynamics due to dispersal polymorphism and dispersal–reproduction trade-offs
title_fullStr Anomalous invasion dynamics due to dispersal polymorphism and dispersal–reproduction trade-offs
title_full_unstemmed Anomalous invasion dynamics due to dispersal polymorphism and dispersal–reproduction trade-offs
title_short Anomalous invasion dynamics due to dispersal polymorphism and dispersal–reproduction trade-offs
title_sort anomalous invasion dynamics due to dispersal polymorphism and dispersal–reproduction trade-offs
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7892423/
https://www.ncbi.nlm.nih.gov/pubmed/33434455
http://dx.doi.org/10.1098/rspb.2020.2825
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