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Host phenology regulates parasite–host demographic cycles and eco‐evolutionary feedbacks
Parasite–host interactions can drive periodic population dynamics when parasites overexploit host populations. The timing of host seasonal activity, or host phenology, determines the frequency and demographic impact of parasite–host interactions, which may govern whether parasites sufficiently overe...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928868/ https://www.ncbi.nlm.nih.gov/pubmed/35342586 http://dx.doi.org/10.1002/ece3.8658 |
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author | MacDonald, Hannelore Brisson, Dustin |
author_facet | MacDonald, Hannelore Brisson, Dustin |
author_sort | MacDonald, Hannelore |
collection | PubMed |
description | Parasite–host interactions can drive periodic population dynamics when parasites overexploit host populations. The timing of host seasonal activity, or host phenology, determines the frequency and demographic impact of parasite–host interactions, which may govern whether parasites sufficiently overexploit hosts to drive population cycles. We describe a mathematical model of a monocyclic, obligate‐killer parasite system with seasonal host activity to investigate the consequences of host phenology on host–parasite dynamics. The results suggest that parasites can reach the densities necessary to destabilize host dynamics and drive cycling as they adapt, but only in some phenological scenarios such as environments with short seasons and synchronous host emergence. Furthermore, only parasite lineages that are sufficiently adapted to phenological scenarios with short seasons and synchronous host emergence can achieve the densities necessary to overexploit hosts and produce population cycles. Host‐parasite cycles also generate an eco‐evolutionary feedback that slows parasite adaptation to the phenological environment as rare advantageous phenotypes can be driven extinct due to a population bottleneck depending on when they are introduced in the cycle. The results demonstrate that seasonal environments can drive population cycling in a restricted set of phenological patterns and provide further evidence that the rate of adaptive evolution depends on underlying ecological dynamics. |
format | Online Article Text |
id | pubmed-8928868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89288682022-03-24 Host phenology regulates parasite–host demographic cycles and eco‐evolutionary feedbacks MacDonald, Hannelore Brisson, Dustin Ecol Evol Research Articles Parasite–host interactions can drive periodic population dynamics when parasites overexploit host populations. The timing of host seasonal activity, or host phenology, determines the frequency and demographic impact of parasite–host interactions, which may govern whether parasites sufficiently overexploit hosts to drive population cycles. We describe a mathematical model of a monocyclic, obligate‐killer parasite system with seasonal host activity to investigate the consequences of host phenology on host–parasite dynamics. The results suggest that parasites can reach the densities necessary to destabilize host dynamics and drive cycling as they adapt, but only in some phenological scenarios such as environments with short seasons and synchronous host emergence. Furthermore, only parasite lineages that are sufficiently adapted to phenological scenarios with short seasons and synchronous host emergence can achieve the densities necessary to overexploit hosts and produce population cycles. Host‐parasite cycles also generate an eco‐evolutionary feedback that slows parasite adaptation to the phenological environment as rare advantageous phenotypes can be driven extinct due to a population bottleneck depending on when they are introduced in the cycle. The results demonstrate that seasonal environments can drive population cycling in a restricted set of phenological patterns and provide further evidence that the rate of adaptive evolution depends on underlying ecological dynamics. John Wiley and Sons Inc. 2022-03-16 /pmc/articles/PMC8928868/ /pubmed/35342586 http://dx.doi.org/10.1002/ece3.8658 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 MacDonald, Hannelore Brisson, Dustin Host phenology regulates parasite–host demographic cycles and eco‐evolutionary feedbacks |
title | Host phenology regulates parasite–host demographic cycles and eco‐evolutionary feedbacks |
title_full | Host phenology regulates parasite–host demographic cycles and eco‐evolutionary feedbacks |
title_fullStr | Host phenology regulates parasite–host demographic cycles and eco‐evolutionary feedbacks |
title_full_unstemmed | Host phenology regulates parasite–host demographic cycles and eco‐evolutionary feedbacks |
title_short | Host phenology regulates parasite–host demographic cycles and eco‐evolutionary feedbacks |
title_sort | host phenology regulates parasite–host demographic cycles and eco‐evolutionary feedbacks |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928868/ https://www.ncbi.nlm.nih.gov/pubmed/35342586 http://dx.doi.org/10.1002/ece3.8658 |
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