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Predicting Evolution over Multiple Generations in Deteriorating Environments Using Evolutionarily Explicit Integral Projection Models

Overview
Journal Evol Appl
Specialty Biology
Date 2021 Nov 8
PMID 34745339
Citations 7
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Abstract

Human impacts on the natural world often generate environmental trends that can have detrimental effects on distributions of phenotypic traits. We do not have a good understanding of how deteriorating environments might impact evolutionary trajectories across multiple generations, even though effects of environmental trends are often significant in the statistical quantitative genetic analyses of phenotypic trait data that are used to estimate additive genetic (co)variances. These environmental trends capture reaction norms, where the same (average) genotype expresses different phenotypic trait values in different environments. Not incorporated into the predictive models typically parameterised from statistical analyses to predict evolution, such as the breeder's equation. We describe how these environmental effects can be incorporated into multi-generational, evolutionarily explicit, structured population models before exploring how these effects can influence evolutionary dynamics. The paper is primarily a description of the modelling approach, but we also show how incorporation into models of the types of environmental trends that human activity has generated can have considerable impacts on the evolutionary dynamics that are predicted.

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References
1.
Wilson A, Pemberton J, Pilkington J, Coltman D, Mifsud D, Clutton-Brock T . Environmental coupling of selection and heritability limits evolution. PLoS Biol. 2006; 4(7):e216. PMC: 1475772. DOI: 10.1371/journal.pbio.0040216. View

2.
Reed T, Schindler D, Waples R . Interacting effects of phenotypic plasticity and evolution on population persistence in a changing climate. Conserv Biol. 2010; 25(1):56-63. PMC: 3084585. DOI: 10.1111/j.1523-1739.2010.01552.x. View

3.
Coulson T, Kendall B, Barthold J, Plard F, Schindler S, Ozgul A . Modeling Adaptive and Nonadaptive Responses of Populations to Environmental Change. Am Nat. 2017; 190(3):313-336. DOI: 10.1086/692542. View

4.
Tuljapurkar S . Population dynamics in variable environments. VI. Cyclical environments. Theor Popul Biol. 1985; 28(1):1-17. DOI: 10.1016/0040-5809(85)90019-x. View

5.
Schindler S, Gaillard J, Gruning A, Neuhaus P, Traill L, Tuljapurkar S . Sex-specific demography and generalization of the Trivers-Willard theory. Nature. 2015; 526(7572):249-52. DOI: 10.1038/nature14968. View