Evolution of reduced dormancy during range expansions

There is increasing evidence that life-history traits can evolve rapidly during range expansion and that this evolution can impact the ecological dynamics of population spread. While dispersal evolution during range expansion has received substantial attention, dormancy (dispersal in time) has not. Here, we use an individual-based model to investigate the evolution of seed dormancy during range expansion. When a population is at spatial equilibrium our model produces results that are consistent with previous theoretical studies: seed dormancy evolves due to kin competition and the degree of dormancy increases as temporal environmental variation increases. During range expansions we consistently observe evolution towards reduced rates of dormancy at the front. Behind the front there is selection for higher rates of dormancy. Notably, the decreased dormancy towards the expanding margin reduces the regional resilience of recently expanded populations to a series of harsh years. We discuss how dormancy evolution during range expansion, and its consequences for spatial population dynamics, may impact other evolutionary responses to environmental change. We end with suggestions for future theoretical and empirical work.

Inbreeding depression drives evolution of dispersal and polyandry

Inbreeding depression, defined as the reduction in fitness components of offspring of related individuals compared to offspring of unrelated individuals, is a widespread phenomenon and has profound demographic and evolutionary consequences. It can reduce the mean fitness of a population and increase extinction risk, and it can affect traits evolution. Inbreeding depression is widely hypothesized to be a key driver of the evolution of, among other traits, dispersal (individual movements potentially leading to spatial gene flow) and polyandry (female mating with multiple males within a single reproductive bout), as mechanisms to avoid inbreeding. In turn, both dispersal and polyandry can change the relatedness structure within and among populations, thus affecting opportunity for inbreeding and consequent evolution of inbreeding depression. However, despite this potential major shared driver, and despite the large amount of both theoretical and empirical work, evolution of dispersal and polyandry given inbreeding have been so far studied separately, and thus we still do not know whether and how dispersal and polyandry affect each other’s evolution, and how they may feed-back onto evolution of inbreeding depression itself. Here, using a genetically-explicit individual-based model, which models realistic distributions of selection and dominance coefficients of deleterious recessive mutations underpinning inbreeding depression, I show that: 1) inbreeding depression indeed drives evolution of dispersal and polyandry; 2) there is a negative feedback between dispersal evolution and polyandry evolution, which therefore evolve as alternative inbreeding avoidance strategies; 3) inbreeding depression is mainly shaped by the level of dispersal, while polyandry has a much more limited effect.

Mutualists construct the ecological conditions that trigger the transition from parasitism

The evolution of mutualism between hosts and initially parasitic symbionts represents a major transition in evolution. Although vertical transmission of symbionts during host reproduction and partner control both favour the stability of mutualism, these mechanisms require specifically evolved features that may be absent during the transition. Therefore, the first steps of the transition from parasitism to mutualism are not fully understood. Spatial structure might be the key to this transition. We explore this hypothesis using a spatially explicit agent-based model. We demonstrate that, starting from a parasitic system with global dispersal, the coevolution between mutualistic effort and local dispersal of hosts and symbionts leads to a stable coexistence between parasites and mutualists. The local dispersal evolution mimics vertical transmission and triggers the formation of mutualistic clusters, counteracting the individual selection level of parasites that maintain global dispersal. However, the transition also requires competition between hosts in order to occur. Indeed, the transition occurs when mutualistic symbionts increase the density of hosts, which strengthens competition between hosts and disfavours parasitic host/symbiont pairs: mutualists create ecological conditions that allow their own spread. Therefore, the transition to mutualism may come from an eco-evolutionary feedback loop involving spatially structured population dynamics.

Desiccation stress acts as cause as well as cost of dispersal in Drosophila melanogaster

Environmental stress is one of the important causes of biological dispersal. At the same time, the process of dispersal itself can incur and/or increase susceptibility to stress for the dispersing individuals. Therefore, in principle, stress can serve as both a cause and a cost of dispersal. Desiccation stress is an environmentally relevant stress faced by many organisms, known to shape their population dynamics and distribution. However, the potentially contrasting roles of desiccation stress as a cause and a cost of dispersal have not been investigated. Furthermore, while desiccation stress often affects organisms in a sex-biased manner, it is not known whether the desiccation-dispersal relationship varies between males and females. We studied the role of desiccation stress as a cause and cost of dispersal in a series of experiments using D. melanogaster adults in two-patch dispersal setups. We were interested in knowing whether (a) dispersers are the individuals that are more susceptible to desiccation stress, (b) dispersers pay a cost in terms of reduced resistance to desiccation stress, (c) dispersal evolution alters the desiccation cost of dispersal, and (d) females pay a reproductive cost of dispersal. For this, we modulated the degree of desiccation stress faced by the flies as well as the provision of rest following a dispersal event. Our data showed that desiccation stress served as a significant cause of dispersal in both sexes. Further investigation revealed an increase in both male and female dispersal propensity with increasing desiccation duration. Next, we found a male-biased cost of dispersal in terms of reduced desiccation resistance. This trend was preserved in dispersal-selected and non-selected controls as well, where the desiccation cost of dispersal in females was very low compared to the males. Finally, we found that the females instead paid a significant reproductive cost of dispersal. Our results highlight the complex relationship between desiccation stress and dispersal, whereby desiccation resistance can show both a positive and a negative association with dispersal. Furthermore, the sex differences observed in these trait associations may translate into differences in movement patterns, thereby giving rise to sex-biased dispersal.

Contrasting effects of ecological and evolutionary processes on range expansions and shifts

Research has conclusively demonstrated the potential for dispersal evolution in range expansions and shifts through a process termed spatial sorting. However, the degree of dispersal evolution observed has varied substantially among organisms. Further, it is unknown how the factors influencing dispersal evolution might impact other ecological processes at play. We use an individual-based model to investigate the effects of the underlying genetics of dispersal and mode of reproduction in range expansions and shifts. Spatial sorting behaves similarly to natural selection in that dispersal evolution increases with sexual selection and loci number. Contrary to our predictions, however, increased dispersal does not always improve a population’s ability to track changing conditions. The mate finding Allee effect inherent to sexual reproduction increases extinction risk during range shifts, counteracting the beneficial effect of increased dispersal evolution. Our results demonstrate the importance of considering both ecological and evolutionary processes for understanding range expansions and shifts.