A distinctive signature of living systems is Darwinian evolution, that is, a propensity to generate as well as self-select individual diversity. To capture this essential feature of life while describing the dynamics of populations, mathematical models must be rooted in the microscopic, stochastic description of discrete individuals characterized by one or several adaptive traits and interacting with each other. The simplest models assume asexual reproduction and haploid genetics: an offspring usually inherits the trait values of her progenitor, except when a mutation causes the offspring to take a mutation step to new trait values; selection follows from ecological interactions among individuals. Here we present a rigorous construction of the microscopic population process that captures the probabilistic dynamics over continuous time of birth, mutation, and death, as influenced by the trait values of each individual, and interactions between individuals. A by-product of this formal construction is a general algorithm for efficient numerical simulation of the individual-level model. Once the microscopic process is in place, we derive different macroscopic models of adaptive evolution. These models differ in the renormalization they assume, i.e. in the limits taken, in specific orders, on population size, mutation rate, mutation step, while rescaling time accordingly. The macroscopic models also differ in their mathematical nature: deterministic, in the form of ordinary, integro-, or partial differential equations, or probabilistic, like stochastic partial differential equations or superprocesses. These models include extensions of Kimura's equation (and of its approximation for small mutation effects) to frequency- and density-dependent selection. A novel class of macroscopic models obtains when assuming that individual birth and death occur on a short timescale compared with the timescale of typical population growth. On a timescale of very rare mutations, we establish rigorously the models of "trait substitution sequences" and their approximation known as the "canonical equation of adaptive dynamics". We extend these models to account for mutation bias and random drift between multiple evolutionary attractors. The renormalization approach used in this study also opens promising avenues to study and predict patterns of life-history allometries, thereby bridging individual physiology, genetic variation, and ecological interactions in a common evolutionary framework.

International audienceWe consider an interacting particle Markov process for Darwinian evolution in an asexual population with non-constant population size, involving a linear birth rate, a density-dependent logistic death rate, and a probability $\mu$ of mutation at each birth event. We introduce a renormalization parameter $K$ scaling the size of the population, which leads, when $K\rightarrow+\infty$, to a deterministic dynamics for the density of individuals holding a given trait. By combining in a non-standard way the limits of large population ($K\rightarrow+\infty$) and of small mutations ($\mu\rightarrow 0$), we prove that a time scales separation between the birth and death events and the mutation events occurs and that the interacting particle microscopic process converges for finite dimensional distributions to the biological model of evolution known as the ``monomorphic trait substitution sequence'' model of adaptive dynamics, which describes the Darwinian evolution in an asexual population as a Markov jump process in the trait space

For general, almost surely absorbed Markov processes, we obtain necessary and sufficient conditions for exponential convergence to a unique quasi-stationary distribution in the total variation norm. These conditions also ensure the existence and exponential ergodicity of the Q-process (the process conditioned to never be absorbed). We apply these results to one-dimensional birth and death processes with catastrophes, multi-dimensional birth and death processes, infinitedimensional population models with Brownian mutations and neutron transport dynamics absorbed at the boundary of a bounded domain.where · is the integer part function and · T V is the total variation norm. Conversely, if there is uniform exponential convergence for the total variation norm in (1.1), then Assumption (A) holds true.

We are interested in the study of models describing the evolution of a polymorphic population with mutation and selection in the specific scales of the biological framework of adaptive dynamics. The population size is assumed to be large and the mutation rate small. We prove that under a good combination of these two scales, the population process is approximated in the long time scale of mutations by a Markov pure jump process describing the successive trait equilibria of the population. This process, which generalizes the so-called trait substitution sequence, is called polymorphic evolution sequence. Then we introduce a scaling of the size of mutations and we study the polymorphic evolution sequence in the limit of small mutations. From this study in the neighborhood of evolutionary singularities, we obtain a full mathematical justification of a heuristic criterion for the phenomenon of evolutionary branching. To this end we finely analyze the asymptotic behavior of 3-dimensional competitive Lotka-Volterra systems