<p>(A) The mean cooperator frequency and (B) population size as a function of time for several values of <i>γ</i> and <i>β</i>. (C) The mean ±SD cooperator frequency as a function of <i>γ</i> for several values of <i>β</i>. (D) Percent runs survived as a function of <i>γ</i> when <i>β</i> = 100 and <i>β</i> = 75.</p
<p>On the left, the mean (±95% CI) rate of change of additive genetic variance (dV<sub>A</sub>/dt; P...
International audienceHow life-history strategies influence the evolution of populations is not well...
A and B: The time evolution of different strategies resulted from the replicator-mutator dynamics A ...
<p>(A) The population cooperator frequency, and (B) the mean genetic quality in the population. Erro...
<p>(A) The percent of runs in which the population survived as a function of the initial cooperator ...
<p>In all simulations species were introduced at the high colonization (low competitive) end of trai...
<p>(A) Initial preferences of the 10% most effective cultural models at the start of a trait's lifet...
This article is a presentation of specific recent results describing scaling limits of individual- b...
<p>Long-term term growth rate predicted by the analytical model in a single patch as a function of r...
How life-history strategies influence the evolution of populations is not well understood. Most exis...
<p>The system size is and the mutation rates are and , respectively. Simulation lasts for time st...
A) Trait evolution after an optimum shift and B) allele frequency dynamics during adaptation from a ...
The objective of this project was to examine the dynamics of population size based on age-specific l...
Gene expression is a stochastic biological processes that controls the different phenotypes of an or...
<p>The co-evolutionary time-dynamics for the level of PI, solicitation allele frequencies and sensit...
<p>On the left, the mean (±95% CI) rate of change of additive genetic variance (dV<sub>A</sub>/dt; P...
International audienceHow life-history strategies influence the evolution of populations is not well...
A and B: The time evolution of different strategies resulted from the replicator-mutator dynamics A ...
<p>(A) The population cooperator frequency, and (B) the mean genetic quality in the population. Erro...
<p>(A) The percent of runs in which the population survived as a function of the initial cooperator ...
<p>In all simulations species were introduced at the high colonization (low competitive) end of trai...
<p>(A) Initial preferences of the 10% most effective cultural models at the start of a trait's lifet...
This article is a presentation of specific recent results describing scaling limits of individual- b...
<p>Long-term term growth rate predicted by the analytical model in a single patch as a function of r...
How life-history strategies influence the evolution of populations is not well understood. Most exis...
<p>The system size is and the mutation rates are and , respectively. Simulation lasts for time st...
A) Trait evolution after an optimum shift and B) allele frequency dynamics during adaptation from a ...
The objective of this project was to examine the dynamics of population size based on age-specific l...
Gene expression is a stochastic biological processes that controls the different phenotypes of an or...
<p>The co-evolutionary time-dynamics for the level of PI, solicitation allele frequencies and sensit...
<p>On the left, the mean (±95% CI) rate of change of additive genetic variance (dV<sub>A</sub>/dt; P...
International audienceHow life-history strategies influence the evolution of populations is not well...
A and B: The time evolution of different strategies resulted from the replicator-mutator dynamics A ...