Abstract
Most traits expressed by organisms, such as gene expression profiles, developmental trajectories, behavioural sequences and reaction norms are function-valued traits (colloquially “phenotypically plastic traits”), since they vary across an individual’s age and in response to various internal and/or external factors (state variables). Furthermore, most organisms live in populations subject to limited genetic mixing and are thus likely to interact with their relatives. We here formalise selection on genetically determined function-valued traits of individuals interacting in a group-structured population, by deriving the marginal version of Hamilton’s rule for function-valued traits. This rule simultaneously gives a condition for the invasion of an initially rare mutant function-valued trait and its ultimate fixation in the population (invasion thus implies substitution). Hamilton’s rule thus underlies the gradual evolution of function-valued traits and gives rise to necessary first-order conditions for their uninvadability (evolutionary stability). We develop a novel analysis using optimal control theory and differential game theory, to simultaneously characterise and compare the first-order conditions of (i) open-loop traits – functions of time (or age) only, and (ii) closed-loop (state-feedback) traits – functions of both time and state variables. We show that closed-loop traits can be represented as the simpler open-loop traits when individuals do not interact or when they interact with clonal relatives. Our analysis delineates the role of state-dependence and interdependence between individuals for trait evolution, which has implications to both life-history theory and social evolution.
Highlights
All biological organisms are open systems exchanging energy, matter, and information with their surrounding
Function-valued traits have been studied in quantitative genetics theory, where the directional selection coefficient on function-valued traits has been derived assuming no interactions between individuals (Kirkpatrick and Heckman, 1989; Gomulkiewicz and Kirkpatrick, 1992; Gomulkiewicz and Beder, 1996; Beder and Gomulkiewicz, 1998). This selection coefficient describes selection over short time-scales and can be decomposed into component-wise descriptions, which allows to describe the direction of selection for each component of a function-valued trait. While this selection coefficient has been connected to long-term evolution and extended to include interactions between individuals in wellmixed populations (Parvinen et al, 2006; Dieckmann et al, 2006), this literature does not distinguish between open-loop and closed-loop traits and it remains unclear how the selection coefficient on a trait connects to the dynamic state constraints underlying trait evolution
In Appendix B.1, we show that the reproductive value satisfies the following partial differential equation (PDE)
Summary
Modeling social insect populations ii: optimal reproductive strategies in annual eusocial insect colonies. Function-valued adaptive dynamics and optimal control theory. Kin selection and natal dispersal in an agestructured population. Natal dispersal and the moulding of senescence by natural selection. Genetic Structure and Selection in Subdivided Populations. Selection and drift in subdivided populations: a straightforward method for deriving diffusion approximations and applications involving dominance, selfing and local extinctions. The application of optimal control theory to the general life history problem. Optimal Control Theory: Applications to Management Science and Economics. Dynamic optimization over infinite-time horizon: web-building strategy in an orb-weaving spider as a case study. Optimal Control Theory with Applications in Economics.
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