Search bioRxiv⌕ Search

bioRxiv · 10.1101/2024.03.28.586951

Life history traits influence the dynamics of genetic diversityin a refugium population undergoing expansion andcontraction

Abstract

Species ranges are dynamic, experiencing expansions, contractions or shifts as a response to habitat changes induced by extrinsic factors such as climate change and, more recently, human activities. While the scientific literature has explored the genetic effects of spatial processes, published studies rarely incorporate life-history traits to study the effect of such changes on species living in the same environments. There is thus a gap in our understanding regarding the variation in genetic diversity patterns among species with distinct life-history traits such as growth rates and generation times, experiencing the same habitat change scenarios. In this study, we first used spatial simulations to investigate the temporal dynamics of genetic diversity within refugium populations experiencing a range expansion followed by a stationary and a contraction period. We explored different scenarios, varying both the speed of contraction and the life-history traits of the simulated species. In addition, we used a simpler panmictic model for which we derived analytical results. Altogether, we identified three temporal dynamics of genetic diversity in the refugium population during the contraction phase: scenarios where genetic diversity i) decreased throughout the contractions, ii) increased for periods that could be greater than thousands of years before plateauing and then decreasing or iii) followed a persistent increasing trend, without any visible effect of the expansion or contraction. We show that these different temporal dynamics can be predicted by comparing the observed expected heterozygosity (He) to the values expected if the species were at equilibrium within the refuge (He refuge) and within the whole landscape (He landscape). We also observe that there are scenarios where a rapid contraction maintains more diversity just at the end of the contraction, as widely believed and as reported in a previous simulation study. However, we also observe the opposite pattern for a wide range of parameters. The widespread idea that observing high diversity levels in a refugium population is due to a recent and rapid habitat loss is thus not necessarily true and will depend on various life history traits and how they relate to habitat change dynamics.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Vishwakarma, R., Sgarlata, G. M., Soriano-Panos, D., Rasteiro, R., Maie, T., Paixao, T., Tournebize, R., Chikhi, L.. 2024-03-31. Life history traits influence the dynamics of genetic diversityin a refugium population undergoing expansion andcontraction. https://doi.org/10.1101/2024.03.28.586951

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Evolutionary dynamics of RNA viruses during persistent infection in Drosophila melanogaster

Persistent viral infections provide an extended window for viral evolution, yet their intra-host trajectories across the host lifespan remain underexplored. Here, we tracked the longitudinal evolution of three single-stranded RNA (ssRNA) viruses (Drosophila A virus [DAV], Drosophila C virus [DCV], and Nora virus) and one double-stranded RNA (dsRNA) virus (Bloomfield virus) during persistent infection in Drosophila melanogaster. By analyzing viral populations across early, intermediate, and late infection stages, we mapped dynamic shifts in the viral quasispecies and the emergence of adaptive mutations. These data demonstrate that long-term persistence drives viral evolution in a viral species-specific manner. DAV evolution was defined by clonal interference, driven by the continuous turnover of competing haplotypes. Nora virus exhibited prolonged evolutionary stasis punctuated by a late-stage sweep, suggesting adaptation to the senescing host environment. In contrast, standard DCV populations were locked under strong purifying selection, where no adaptive mutations were detected. However, this constraint collapsed in high-titer DCV infections, triggering extensive mutational diversification. Distinct from the ssRNA dynamics, the multi-segmented dsRNA Bloomfield virus maintained higher sequence fidelity and a stable genomic formula. Ultimately, these results demonstrate that viral evolution during persistent infection is governed by the interplay between specific host-pathogen interactions and the physiological decline of the host.

evolutionary biology↗

A new cell type facilitated live-bearing and multiple independent origins of placentation in fish

The origin of new organs has fascinated biologists since Darwin. Yet the molecular and evolutionary steps that give rise to new organs remain difficult to resolve, largely because most organs have ancient origins. The fish family Poeciliidae offers a rare exception. Within poeciliids, placentas have independently evolved at least nine times, including within the last ~10 million years. Here, we study the molecular and cellular drivers of five independent origins of a placenta, using pairs of sister species with and without a placenta. We identified a new maternal cell type that emerged in the common ancestor of poeciliids and likely enabled the family to transition from egg-laying to live-bearing through egg retention. This new cell type originated by partly co-opting the existing gene regulatory network of another ovarian cell type. Subsequently, this same new maternal cell type, together with the embryonic yolk sac, was repeatedly and independently co-opted to form a placenta in all five origins. The evolution of these placentas involved high levels of convergence at the pathway level (e.g., lipid metabolism and vesicle-mediated transport), although these functional changes relied primarily on distinct genes across species. Our analyses show how the evolution and modification of a new cell type enabled the evolution of live birth and placentation, providing the cellular and genetic foundations for the repeated evolution of a new organ.

evolutionary biology↗

The extracellular morphology and behaviour of the last common ancestor of animals and choanoflagellates

Choanoflagellates, the closest known living relatives of animals, provide a powerful comparative system for investigating the evolution of extracellular morphology and cell behaviour on the animal stem lineage. Although all choanoflagellates share a conserved cellular architecture including a flagellum and collar of microvilli, they display a wide diversity of extracellular structures and behaviours throughout the life cycle. Their extracellular features, historically used for species identification, have long been suspected to reflect a mixture of evolutionary inheritance and ecological plasticity. Yet, the majority of choanoflagellate diversity remains undescribed, and the extent to which their extracellular traits map onto their phylogeny has remained unclear, impeding comparative reconstructions of the evolutionary history of extracellular structures with the earliest animals. Here, we integrate super-resolution fluorescence imaging, electron microscopy and transcriptomic analysis to characterize the extracellular structures and behaviours across both currently described lineages of choanoflagellates (Craspedida and Acanthoecida), by studying pairs of closely related species in conjunction with novel isolates representing previously unexplored clades. Our results reveal strong conservation of extracellular morphology between close relatives, whereas deeper evolutionary distances uncover unexpected innovations, such as sheath-like layers, bipartite thecae, crawling stages and atypical inverted division patterns. Furthermore, the inclusion of early-branching taxa sister to the loricates supports the hypothesis that the silicified extracellular lorica is a derived trait rather than an ancestral feature. Together, our findings suggest that the last choanoflagellate common ancestor possessed an organic non-silicified extracellular covering composed of one or more layers and that it was capable of both swimming and crawling behaviours, refining the cellular context from which animals evolved.

evolutionary biology↗