In this work we describe a new model for the evolution of a diploid structured population backwards in time that allows for large migrations and uneven offspring distributions. The model generalizes both the mean-field model of Birkner et al. [\textit{Electron. J. Probab.} 23: 1-44 (2018)] and the haploid structured model of Möhle [\textit{Theor. Popul. Biol.} 2024 Apr:156:103-116]. We show convergence, with mild conditions on the joint distribution of offspring frequencies and migrations, of gene genealogies conditional on the pedigree to a time-inhomogeneous coalescent process driven by a Poisson point process $Ψ$ that records the timing and scale of large migrations and uneven offspring distributions. This quenched scaling limit demonstrates a significant difference in the predictions of the classical annealed theory of structured coalescent processes. In particular, the annealed and quenched scaling limits coincide if and only if these large migrations and uneven offspring distributions are absent. The proof proceeds by the method of moments and utilizes coupling techniques from the theory of random walks in random environments. Several examples are given and their quenched scaling limits established.
We review recent progress in the understanding of the role of multiple- and simultaneous multiple merger coalescents as models for the genealogy in idealised and real populations with exceptional reproductive behaviour. In particular, we discuss models with `skewed offspring distribution' (or under other non-classical evolutionary forces) which lead in the single locus haploid case to multiple merger coalescents, and in the multi-locus diploid case to simultaneous multiple merger coalescents. Further, we discuss inference methods under the infinitely-many sites model which allow both model sel…
We study the following model for a diploid population of constant size $N$: Every individual carries a random number of (genetic) elements. Upon a reproduction event each of the two parents passes each element independently with probability $\tfrac 12$ on to the offspring. We study the process $X^N = (X^N(1), X^N(2),...)$, where $X_t^N(k)$ is the frequency of individuals at time $t$ that carry $k$ elements, and prove convergence (in some weak sense) of $X^N$ jointly with its empirical first moment $Z^N$ to the ``slow-fast'' system $(Z,X)$, where $X_t = \text{Poi}(Z_t)$ and $Z$ evolves accordin…
Consider a population evolving as a critical continuous-time Galton-Watson (GW) tree. Conditional on the population surviving until a large time $T$, sample $k$ individuals uniformly at random (without replacement) from amongst those alive at time $T$. What is the genealogy of this sample of individuals? In cases where the offspring distribution has finite variance, the probabilistic properties of the joint ancestry of these $k$ particles are well understood, as seen in \cite{HJR20, J19}. In the present article, we study the joint ancestry of a sample of $k$ particles under the following regim…
The $N$-particle branching random walk is a discrete time branching particle system with selection. We have $N$ particles located on the real line at all times. At every time step each particle is replaced by two offspring, and each offspring particle makes a jump of non-negative size from its parent's location, independently from the other jumps, according to a given jump distribution. Then only the $N$ rightmost particles survive; the other particles are removed from the system to keep the population size constant. Inspired by work of J. Bérard and P. Maillard, we examine the long term behav…
