» Articles » PMID: 35603024

Escalating the Conflict? Intersex Genetic Correlations Influence Adaptation to Environmental Change in Facultatively Migratory Populations

Overview
Journal Evol Appl
Specialty Biology
Date 2022 May 23
PMID 35603024
Authors
Affiliations
Soon will be listed here.
Abstract

Males and females are often subject to different and even opposing selection pressures. When a given trait has a shared genetic basis between the sexes, sexual conflict (antagonism) can arise. This can result in significant individual-level fitness consequences that might also affect population performance, whilst anthropogenic environmental change can further exacerbate maladaptation in one or both sexes driven by sexual antagonism. Here, we develop a genetically explicit eco-evolutionary model using an agent-based framework to explore how a population of a facultatively migratory fish species (brown trout ) adapts to environmental change across a range of intersex genetic correlations for migration propensity, which influence the magnitude of sexual conflict. Our modelled focal trait represents a condition threshold governing whether individuals adopt a resident or anadromous (sea migration) tactic. Anadromy affords potential size-mediated reproductive advantages to both males and females due to improved feeding opportunities at sea, but these can be undermined by high background marine mortality and survival/growth costs imposed by marine parasites (sea lice). We show that migration tactic frequency for a given set of environmental conditions is strongly influenced by the intersex genetic correlation, such that one sex can be dragged off its optimum more than the other. When this occurred in females in our model, population productivity was substantially reduced, but eco-evolutionary outcomes were altered by allowing for sneaking behaviour in males. We discuss real-world implications of our work given that anadromous salmonids are regularly challenged by sea lice infestations, which might act synergistically with other stressors such as climate change or fishing that impact marine performance, driving populations towards residency and potentially reduced resilience.

Citing Articles

Whole-Genome Resequencing Reveals Polygenic Signatures of Directional and Balancing Selection on Alternative Migratory Life Histories.

Moran P, Colgan T, Phillips K, Coughlan J, McGinnity P, Reed T Mol Ecol. 2024; 33(23):e17538.

PMID: 39497337 PMC: 11589691. DOI: 10.1111/mec.17538.


Competitive interactions affect introgression and population viability amidst maladaptive hybridization.

Reed T, Kane A, McGinnity P, OSullivan R Evol Appl. 2024; 17(7):e13746.

PMID: 38957310 PMC: 11217556. DOI: 10.1111/eva.13746.


Evolutionary rescue from climate change: male indirect genetic effects on lay-dates and their consequences for population persistence.

Murray M, Wright J, Araya-Ajoy Y Evol Lett. 2024; 8(1):137-148.

PMID: 38487362 PMC: 10939382. DOI: 10.1093/evlett/qrad022.


Importance of interindividual interactions in eco-evolutionary population dynamics: The rise of demo-genetic agent-based models.

Lamarins A, Fririon V, Folio D, Vernier C, Daupagne L, Labonne J Evol Appl. 2022; 15(12):1988-2001.

PMID: 36540635 PMC: 9753837. DOI: 10.1111/eva.13508.


Escalating the conflict? Intersex genetic correlations influence adaptation to environmental change in facultatively migratory populations.

Kane A, Ayllon D, OSullivan R, McGinnity P, Reed T Evol Appl. 2022; 15(5):773-789.

PMID: 35603024 PMC: 9108303. DOI: 10.1111/eva.13368.

References
1.
Bell D, Kovach R, Robinson Z, Whiteley A, Reed T . The ecological causes and consequences of hard and soft selection. Ecol Lett. 2021; 24(7):1505-1521. DOI: 10.1111/ele.13754. View

2.
Cline T, Ohlberger J, Schindler D . Effects of warming climate and competition in the ocean for life-histories of Pacific salmon. Nat Ecol Evol. 2019; 3(6):935-942. DOI: 10.1038/s41559-019-0901-7. View

3.
Boyle W . Partial migration in birds: tests of three hypotheses in a tropical lekking frugivore. J Anim Ecol. 2008; 77(6):1122-8. DOI: 10.1111/j.1365-2656.2008.01451.x. View

4.
Tomkins J, Hazel W . The status of the conditional evolutionarily stable strategy. Trends Ecol Evol. 2007; 22(10):522-8. DOI: 10.1016/j.tree.2007.09.002. View

5.
Kuparinen A, Hutchings J . Genetic architecture of age at maturity can generate divergent and disruptive harvest-induced evolution. Philos Trans R Soc Lond B Biol Sci. 2016; 372(1712). PMC: 5182431. DOI: 10.1098/rstb.2016.0035. View