2013
DOI: 10.1016/j.tpb.2012.12.003
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Dynamics of sexual populations structured by a space variable and a phenotypical trait

Abstract: We study sexual populations structured by a phenotypic trait and a space variable, in a non-homogeneous environment. Departing from a structured population equation we perform a hydrodynamic-type limit to derive a model close to an existing model of theoretical biology. We then perform a further simplification to obtain a model depending on only one parameter that indicates how fast the environment is changing. We show that depending on this parameter, there exist either propagating waves, where the population… Show more

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Cited by 42 publications
(51 citation statements)
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“…We consider self-compatible, hermaphroditic plants with no seed bank. Following previous analytical models (18,19,21,23,24,(30)(31)(32), we consider the continuous-time evolution of a population in a continuous space structured by a phenotypic trait, which determines fitness. Population density at time t and at location x is denoted nðx, tÞ; the mean phenotypic trait is denoted zðx, tÞ (see Table 1 for a summary of the notation).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…We consider self-compatible, hermaphroditic plants with no seed bank. Following previous analytical models (18,19,21,23,24,(30)(31)(32), we consider the continuous-time evolution of a population in a continuous space structured by a phenotypic trait, which determines fitness. Population density at time t and at location x is denoted nðx, tÞ; the mean phenotypic trait is denoted zðx, tÞ (see Table 1 for a summary of the notation).…”
Section: Methodsmentioning
confidence: 99%
“…Building on previous quantitative genetic models in continuous space (18,19,21,23,24,(30)(31)(32), we analyze here the effect of the distance of pollen dispersal relative to seed dispersal on the responses of a population to a changing environment. We assume that pollen does not directly limit plant fecundity but that population dynamics depend on local adaptation.…”
Section: Significancementioning
confidence: 99%
“…This provides a way to study a small adaptation potential while scaling the environment accordingly. This small adaptation limit has already been studied by Mirrahimi and Raoul (2013) and there is an explicit expression for the propagation speed for such low adaptation scenarios, given by:…”
Section: Explicit Approximation Of Propagation Speeds Under Various Amentioning
confidence: 99%
“…The blue hatched area is the zone in the parameter space where the difference between propagation speed in Kirkpatrick and Barton's model and Fisher-KPP's model is at most 0.1, marking the strong adaptation regime; the red hatched area is where propagation speed in Kirkpatrick and Barton's model is well approximated (i.e. the difference is at most 0.1) by the formula by Mirrahimi and Raoul (2013), i.e., given by (3), marking the weak adaptation regime.…”
Section: Relating Propagation Speeds To Adaptation Regimesmentioning
confidence: 99%
“…The analysis of nonlinear reaction-diffusion systems by maximal exploitation of relations to the ordinary diffusion equation has parallels in recent work of Alfaro and Carles [42] on non-local reaction-diffusion equations, while the notion of interacting, evolving phenotype distributions (in a genetic, rather than epigentic context, and with a somewhat different mathematical formulation) was pursued by May and Nowak two decades ago [43][44][45]. The inclusion of variation across physical space as well as across phenotype space or the incorporation of non-local couplings with more structure than in our simple coupling via the total population could produce a richer class of behaviours [46][47][48][49][50][51][52][53][54][55].…”
Section: Laplace Transform Analysismentioning
confidence: 99%