Cargando…

The Joint Evolution of Herbivory Defense and Mating System in Plants: A Simulation Approach

Agricultural losses brought about by insect herbivores can be reduced by understanding the strategies that plants use against insect herbivores. The two main strategies that plants use against herbivory are resistance and tolerance. They are, however, predicted to be mutually exclusive, yet numerous...

Descripción completa

Detalles Bibliográficos
Autores principales: Sandoval-Castellanos, Edson, Núñez-Farfán, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9919119/
https://www.ncbi.nlm.nih.gov/pubmed/36771638
http://dx.doi.org/10.3390/plants12030555
_version_ 1784886744945000448
author Sandoval-Castellanos, Edson
Núñez-Farfán, Juan
author_facet Sandoval-Castellanos, Edson
Núñez-Farfán, Juan
author_sort Sandoval-Castellanos, Edson
collection PubMed
description Agricultural losses brought about by insect herbivores can be reduced by understanding the strategies that plants use against insect herbivores. The two main strategies that plants use against herbivory are resistance and tolerance. They are, however, predicted to be mutually exclusive, yet numerous populations have them both (hence a mixed defense strategy). This has been explained, among other alternatives, by the non-linear behavior of the costs and benefits of resistance and tolerance and their interaction with plants’ mating system. Here, we studied how non-linearity and mating system affect the evolutionary stability of mixed defense strategies by means of agent-based model simulations. The simulations work on a novel model that was built upon previous ones. It incorporates resistance and tolerance costs and benefits, inbreeding depression, and a continuously scalable non-linearity. The factors that promoted the evolutionary stability of mixed defense strategies include a multiplicative allocation of costs and benefits of resistance and tolerance, a concave non-linearity, non-heritable selfing, and high tolerance costs. We also found new mechanisms, enabled by the mating system, that are worth considering for empirical studies. One was a double trade-off between resistance and tolerance, predicted as a consequence of costs duplication and the inducibility of tolerance, and the other was named the resistance-cost-of-selfing, a term coined by us, and was derived from the duplication of costs that homozygous individuals conveyed when a single resistance allele provided full protection.
format Online
Article
Text
id pubmed-9919119
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-99191192023-02-12 The Joint Evolution of Herbivory Defense and Mating System in Plants: A Simulation Approach Sandoval-Castellanos, Edson Núñez-Farfán, Juan Plants (Basel) Article Agricultural losses brought about by insect herbivores can be reduced by understanding the strategies that plants use against insect herbivores. The two main strategies that plants use against herbivory are resistance and tolerance. They are, however, predicted to be mutually exclusive, yet numerous populations have them both (hence a mixed defense strategy). This has been explained, among other alternatives, by the non-linear behavior of the costs and benefits of resistance and tolerance and their interaction with plants’ mating system. Here, we studied how non-linearity and mating system affect the evolutionary stability of mixed defense strategies by means of agent-based model simulations. The simulations work on a novel model that was built upon previous ones. It incorporates resistance and tolerance costs and benefits, inbreeding depression, and a continuously scalable non-linearity. The factors that promoted the evolutionary stability of mixed defense strategies include a multiplicative allocation of costs and benefits of resistance and tolerance, a concave non-linearity, non-heritable selfing, and high tolerance costs. We also found new mechanisms, enabled by the mating system, that are worth considering for empirical studies. One was a double trade-off between resistance and tolerance, predicted as a consequence of costs duplication and the inducibility of tolerance, and the other was named the resistance-cost-of-selfing, a term coined by us, and was derived from the duplication of costs that homozygous individuals conveyed when a single resistance allele provided full protection. MDPI 2023-01-26 /pmc/articles/PMC9919119/ /pubmed/36771638 http://dx.doi.org/10.3390/plants12030555 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sandoval-Castellanos, Edson
Núñez-Farfán, Juan
The Joint Evolution of Herbivory Defense and Mating System in Plants: A Simulation Approach
title The Joint Evolution of Herbivory Defense and Mating System in Plants: A Simulation Approach
title_full The Joint Evolution of Herbivory Defense and Mating System in Plants: A Simulation Approach
title_fullStr The Joint Evolution of Herbivory Defense and Mating System in Plants: A Simulation Approach
title_full_unstemmed The Joint Evolution of Herbivory Defense and Mating System in Plants: A Simulation Approach
title_short The Joint Evolution of Herbivory Defense and Mating System in Plants: A Simulation Approach
title_sort joint evolution of herbivory defense and mating system in plants: a simulation approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9919119/
https://www.ncbi.nlm.nih.gov/pubmed/36771638
http://dx.doi.org/10.3390/plants12030555
work_keys_str_mv AT sandovalcastellanosedson thejointevolutionofherbivorydefenseandmatingsysteminplantsasimulationapproach
AT nunezfarfanjuan thejointevolutionofherbivorydefenseandmatingsysteminplantsasimulationapproach
AT sandovalcastellanosedson jointevolutionofherbivorydefenseandmatingsysteminplantsasimulationapproach
AT nunezfarfanjuan jointevolutionofherbivorydefenseandmatingsysteminplantsasimulationapproach