Resource Variation Within and Between Patches: Where Exploitation Competition, Local Adaptation, and Kin Selection Meet.

AbstractIn patch- or habitat-structured populations, different processes can favor adaptive polymorphism at different scales. While spatial heterogeneity can generate spatially disruptive selection favoring variation between patches, local competition can lead to locally disruptive selection promoting variation within patches. So far, almost all theory has studied these two processes in isolation. Here, we use mathematical modeling to investigate how resource variation within and between habitats influences the evolution of variation in a consumer population where individuals compete in finite patches connected by dispersal. We find that locally and spatially disruptive selection typically act in concert, favoring polymorphism under a wider range of conditions than when in isolation. But when patches are small and dispersal between them is low, kin competition inhibits the emergence of polymorphism, especially when the latter is driven by local competition for resources. We further use our model to clarify what comparisons between trait and neutral genetic differentiation (QST/FST comparisons) can tell about the nature of selection. Overall, our results help us understand the interaction between two major drivers of polymorphism: locally and spatially disruptive selection, and how this interaction is modulated by the unavoidable effects of kin selection under limited dispersal.

The impact of dormancy on evolutionary branching.

In this paper, we investigate the consequences of dormancy in the 'rare mutation' and 'large population' regime of stochastic adaptive dynamics. Starting from an individual-based micro-model, we first derive the Polymorphic Evolution Sequence of the population, based on a previous work by Baar and Bovier (2018). After passing to a second 'small mutations' limit, we arrive at the Canonical Equation of Adaptive Dynamics, and state a corresponding criterion for evolutionary branching, extending a previous result of Champagnat and Méléard (2011). The criterion allows a quantitative and qualitative analysis of the effects of dormancy in the well-known model of Dieckmann and Doebeli (1999) for sympatric speciation. In fact, quite an intuitive picture emerges: Dormancy enlarges the parameter range for evolutionary branching, increases the carrying capacity and niche width of the post-branching sub-populations, and, depending on the model parameters, can either increase or decrease the 'speed of adaptation' of populations. Finally, dormancy increases diversity by increasing the genetic distance between subpopulations.

Spatial social dilemmas promote diversity.

Cooperative investments in social dilemmas can spontaneously diversify into stably coexisting high and low contributors in well-mixed populations. Here we extend the analysis to emerging diversity in (spatially) structured populations. Using pair approximation, we derive analytical expressions for the invasion fitness of rare mutants in structured populations, which then yields a spatial adaptive dynamics framework. This allows us to predict changes arising from population structures in terms of existence and location of singular strategies, as well as their convergence and evolutionary stability as compared to well-mixed populations. Based on spatial adaptive dynamics and extensive individual-based simulations, we find that spatial structure has significant and varied impacts on evolutionary diversification in continuous social dilemmas. More specifically, spatial adaptive dynamics suggests that spontaneous diversification through evolutionary branching is suppressed, but simulations show that spatial dimensions offer new modes of diversification that are driven by an interplay of finite-size mutations and population structures. Even though spatial adaptive dynamics is unable to capture these new modes, they can still be understood based on an invasion analysis. In particular, population structures alter invasion fitness and can open up new regions in trait space where mutants can invade, but that may not be accessible to small mutational steps. Instead, stochastically appearing larger mutations or sequences of smaller mutations in a particular direction are required to bridge regions of unfavorable traits. The net effect is that spatial structure tends to promote diversification, especially when selection is strong.

Complex life cycles drive community assembly through immigration and adaptive diversification.

Most animals undergo ontogenetic niche shifts during their life. Yet, standard ecological theory builds on models that ignore this complexity. Here, we study how complex life cycles, where juvenile and adult individuals each feed on different sets of resources, affect community richness. Two different modes of community assembly are considered: gradual adaptive evolution and immigration of new species with randomly selected phenotypes. We find that under gradual evolution complex life cycles can lead to both higher and lower species richness when compared to a model of species with simple life cycles that lack an ontogenetic niche shift. Thus, complex life cycles do not per se increase the scope for gradual adaptive diversification. However, complex life cycles can lead to significantly higher species richness when communities are assembled trough immigration, as immigrants can occupy isolated peaks of the dynamic fitness landscape that are not accessible via gradual evolution.

Beyond simple adaptation: Incorporating other evolutionary processes and concepts into eco-evolutionary dynamics.

Studies of eco-evolutionary dynamics have integrated evolution with ecological processes at multiple scales (populations, communities and ecosystems) and with multiple interspecific interactions (antagonistic, mutualistic and competitive). However, evolution has often been conceptualised as a simple process: short-term directional adaptation that increases population growth. Here we argue that diverse other evolutionary processes, well studied in population genetics and evolutionary ecology, should also be considered to explore the full spectrum of feedback between ecological and evolutionary processes. Relevant but underappreciated processes include (1) drift and mutation, (2) disruptive selection causing lineage diversification or speciation reversal and (3) evolution driven by relative fitness differences that may decrease population growth. Because eco-evolutionary dynamics have often been studied by population and community ecologists, it will be important to incorporate a variety of concepts in population genetics and evolutionary ecology to better understand and predict eco-evolutionary dynamics in nature.

The Adaptation Front Equation Explains Innovation-Driven Taxonomic Turnovers and Living Fossilization.

AbstractEvolutionary taxonomic turnovers are often associated with innovations beneficial in various ecological niches. Such innovations can repeatedly occur in species occupying optimum niches for a focal species group, resulting in their repeated diversifications and species flows from optimum to suboptimum niches, at the expense of less innovated ones. By combining species packing theory and adaptive dynamics theory, we develop an equation that allows analytical prediction for such innovation-driven species flows over a niche space of arbitrary dimension under a unimodal carrying capacity distribution. The developed equation and simulated evolution show that central niches (with the highest carrying capacities) tend to attain the fastest innovation speeds to become biodiversity sources. Species that diverge from the central niches outcompete the indigenous species in peripheral niches. The outcompeted species become extinct or evolve directionally toward far more peripheral niches. Because of this globally acting process over niches, species occupying the most peripheral niches are the least innovated and have deep divergence times from their closest relatives, and thus they correspond to living fossils. The extension of this analysis for multiple geographic regions shows that living fossils are also expected in geographically peripheral regions for the focal species group.

Evolution of dispersal under spatio-temporal heterogeneity.

Theoretical studies over the past decades have revealed various factors that favor or disfavor the evolution of dispersal. Among these, environmental heterogeneity is one driving force that can impact dispersal traits, because dispersing individuals can obtain a fitness benefit through finding better environments. Despite this potential benefit, some previous works have shown that the existence of spatial heterogeneity hinders evolution of dispersal. On the other hand, temporal heterogeneity has been shown to promote dispersal through a bet-hedging mechanism. When they are combined in a patch-structured population in which the quality of each patch varies over time independently of the others, it has been shown that spatiotemporal heterogeneity can favor evolution of dispersal. When individuals can use patch quality information so that dispersal decision is conditional, the evolutionary outcome can be different since individuals have options to disperse more/less offspring from bad/good patches. In this paper, we generalize the model and results of previous studies. We find richer dynamics including bistable evolutionary dynamics when there is arrival bias towards high-productivity patches. Then we study the evolution of conditional dispersal strategy in this generalized model. We find a surprising result that no offspring will disperse from a patch whose productivity was low when these offspring were born. In addition to mathematical proofs, we also provide intuition behind this initially counter-intuitive result based on reproductive-value arguments. Dispersal from high-productivity patches can evolve, and its parameter dependence behaves similarly, but not identically, to the case of unconditional dispersal. Our results unveil an importance of whether or not individuals can use patch quality information in dispersal evolution.

Evolution of dispersal in a spatially heterogeneous population with finite patch sizes.

Dispersal is one of the fundamental life-history strategies of organisms, so understanding the selective forces shaping the dispersal traits is important. In the Wright's island model, dispersal evolves due to kin competition even when dispersal is costly, and it has traditionally been assumed that the living conditions are the same everywhere. To study the effect of spatial heterogeneity, we extend the model so that patches may receive different amounts of immigrants, foster different numbers of individuals, and give different reproduction efficiency to individuals therein. We obtain an analytical expression for the fitness gradient, which shows that directional selection consists of three components: As in the homogeneous case, the direct cost of dispersal selects against dispersal and kin competition promotes dispersal. The additional component, spatial heterogeneity, more precisely the variance of so-called relative reproductive potential, tends to select against dispersal. We also obtain an expression for the second derivative of fitness, which can be used to determine whether there is disruptive selection: Unlike the homogeneous case, we found that divergence of traits through evolutionary branching is possible in the heterogeneous case. Our numerical explorations suggest that evolutionary branching is promoted more by differences in patch size than by reproduction efficiency. Our results show the importance of the existing spatial heterogeneity in the real world as a key determinant in dispersal evolution.

The enrichment paradox in adaptive radiations: Emergence of predators hinders diversification in resource rich environments.

Adaptive radiations are known for rapid niche diversification in response to ecological opportunity. While most resources usually exist prior to adaptive radiation, novel niches associated with novel resources can be created as a clade diversifies. For example, in African lake cichlid radiations some species prey upon other species of the clade (intraclade consumers). Using a trait-based eco-evolutionary model, we investigate the evolution of intraclade consumers in adaptive radiations and the effect of this novel trophic interaction on the diversification process of the radiating clade. We find that the evolutionary emergence of intraclade consumers halts the diversification processes of other ecomorphs as a result of increased top-down control of density. Because high productivity enables earlier evolution of intraclade consumers, highly productive environments come to harbour less species-rich radiations than comparable radiations in less productive environments. Our results reveal how macroevolutionary and community patterns can emerge from ecological and microevolutionary processes.

Evolutionary coexistence in a metacommunity: Competition-colonization trade-off, ownership effects, environmental fluctuations.

We study the adaptive dynamics of the colonization rate of species living in a patchy habitat when there is a trade-off with the competitive strength for individual patches. To that end, we formulate a continuous-time competition-colonization model that also includes ownership effects as well as random disturbance affecting the mortality rate. We find that intermediate disturbance (as measured by the fluctuation intensity of the mortality rate), a strong competition-colonization trade-off, and a weak ownership effect are necessary conditions for evolutionary branching and hence for the emergence of polymorphisms (i.e., coexistence) by small evolutionary steps. Specifically, concerning ownership we find that with low-intermediate disturbance, a weak ownership advantage favours evolutionary branching while ownership disadvantage does not. This asymmetry disappears at the higher-intermediate disturbance. Moreover, at a low-intermediate disturbance, the effect of the strength of the competition-colonization trade-off on evolutionary branching is non-monotonic disappears because the possibility of branching disappears again when the trade-off is too strong. We also find that there can be multiple evolutionary attractors for polymorphic populations, each with its own basin of attraction. With small but non-zero random evolutionary steps and depending on the initial polymorphic condition just after branching, a coevolutionary trajectory may come arbitrarily close to the shared boundary of two such basins and may even jump from one side to the other, which can lead to various kinds of long-term evolutionary dynamics, including evolutionary branching-extinction cycles.

The importance of ecological dynamics in evolutionary processes: A host-bacteriophage model revisited.

A recent study of adaptive dynamics of lysis propensity in temperate phages suggested that full lysogeny emerges as the outcome of bacteriophage evolution in a simple host-phage system. The conclusion is based on the premise that mutant strains necessarily appear in equilibrium host-phage environments. Revisiting the model, we show that the ecological system exhibits richer asymptotic dynamics and that, in a certain parameter regime, evolution may in fact drive lysis propensity towards an evolutionary singularity in which a non-zero proportion of phages initiate infection in a lytic cycle. These singularities act as points of evolutionary diversification, leading to periodic coexistence of two distinct phage strains on the evolutionary time-scale. One of the two strains in the dimorphic evolutionary singularity is fully lysogenic (in the sense that cell infection always leads to lysogeny), while the other is partially lytic. Our study thus highlights the importance of ecological interactions as a driver of evolution.

Coevolutionary dynamics of host-pathogen interaction with density-dependent mortality.

This study explores the coevolutionary dynamics of host-pathogen interaction based on a susceptible-infected population model with density-dependent mortality. We assume that both the host's resistance and the pathogen's virulence will adaptively evolve, but there are inevitable costs in terms of host birth rate and disease-related mortality rate. Particularly, it is assumed that both the host resistance and pathogen virulence can affect the transmission rate. By using the approach of adaptive dynamics and numerical simulation, we find that the finally coevolutionary outcome depends on the strength of host-pathogen asymmetric interaction, the curvature of trade-off functions, and the intensity of density-dependent natural mortality. To be specific, firstly, we find that if the strengths of host-pathogen asymmetric interaction and disease-related mortality are relatively weak, or the density-dependent natural mortality is relatively strong, then the host resistance and pathogen virulence will evolve to a continuously stable strategy. However, if the strength of host-pathogen asymmetric interaction and disease-related mortality becomes stronger, then the host resistance and pathogen virulence will evolve periodically. Secondly, we find that if the intensities of both the birth rate trade-off function and the density-dependent natural mortality are relatively weak, but the strength of host-pathogen asymmetric interaction becomes relatively strong, then the evolution of host resistance will have a relatively strongly accelerating benefit, the evolutionary branching of host resistance will first arise. However, if the strength of host-pathogen asymmetric interaction is relatively weak, but the intensity of the trade-off function of disease-related mortality becomes relatively strong, then the evolution of pathogen virulence will have a relatively strongly decelerating cost, and the evolutionary branching of pathogen virulence will first arise. Thirdly, after the evolutionary branching of host resistance and pathogen virulence, we further study the coevolutionary dynamics of two-hosts-one-pathogen interaction and one-host-two-pathogens interaction. We find that if the evolutionary branching of host resistance arises firstly, then the finally evolutionary outcome contains a dimorphic host and a monomorphic pathogen population. If the evolutionary branching of pathogen virulence arises firstly, then the finally evolutionary outcome may contain a monomorphic host and a dimorphic pathogen population.

How Does Joint Evolution of Consumer Traits Affect Resource Specialization?

Consumers regularly experience trade-offs in their ability to find, handle, and digest different resources. Evolutionary ecologists recognized the significance of this observation for the evolution and maintenance of biological diversity long ago and continue to elaborate on the conditions under which to expect one or several specialists, generalists, or combinations thereof. Existing theory based on a single evolving trait predicts that specialization requires strong trade-offs such that generalists perform relatively poorly, while weak trade-offs favor a single generalist. Here, we show that this simple dichotomy does not hold true under joint evolution of two or more foraging traits. In this case, the boundary between trade-offs resulting in resource specialists and resource generalists is shifted toward weaker trade-off curvatures. In particular, weak trade-offs can result in evolutionary branching, leading to the evolution of two coexisting resource specialists, while the evolution of a single resource generalist requires particularly weak trade-offs. These findings are explained by performance benefits due to epistatic trait interactions enjoyed by phenotypes that are specialized in more than one trait for the same resource.

Fecundity-Longevity Trade-Off, Vertical Transmission, and Evolution of Virulence in Sterilizing Pathogens.

Sterilizing pathogens are common, yet studies focused on how such pathogens respond adaptively to fecundity reductions caused in their hosts are rare. Here we assume that the infected hosts, as a result of redistributing energy resources saved by reduced fecundity, have increased longevity and focus on exploring the consequences of such a fecundity-longevity trade-off on sterility virulence evolution in the pathogens. We find that the trade-off itself cannot prevent the evolution of full sterilization. Therefore, we allow for vertical transmission and reveal that the fecundity-longevity trade-off strongly determines the threshold efficiency of vertical transmission above which partial host sterilization evolves. Partial sterilization may appear as an intermediate level of sterility virulence or as a stable dimorphism at which avirulent and highly virulent strains coexist. The fecundity-longevity trade-off significantly contributes to determining the actual outcome, in many cases countering predictions made in the absence of this trade-off. It is known that in well-mixed populations, partial sterilization may evolve in pathogens under a combination of horizontal and vertical transmission. Our study highlights that this is independent of the form of horizontal transmission and the type of density dependence in host demography and that the fecundity-longevity trade-off is an important player in sterility virulence evolution.

The effect of temporal fluctuations on the evolution of host tolerance to parasitism.

There are many mechanisms that hosts can evolve to defend against parasites, two of which are resistance and tolerance. These defences often have different evolutionary behaviours, and it is important to consider how each individual mechanism may respond to changes in environment. In particular, host defence through tolerance is predicted to be unlikely to lead to variation, despite many observations of diversity in both animal and plant systems. Hence understanding the drivers of diversity in host defence and parasite virulence is vital for predicting future evolutionary changes in infectious disease dynamics. It has been suggested that heterogeneous environments might generally promote diversity, but the effect of temporal fluctuations has received little attention theoretically or empirically, and there has been no examination of how temporal fluctuations affects the evolution of host tolerance. In this study, we use a mathematical model to investigate the evolution of host tolerance in a temporally fluctuating environment. We show that investment in tolerance increases in more variable environments, giving qualitatively different evolutionary behaviours when compared to resistance. Once seasonality is introduced evolutionary branching though tolerance can occur and create diversity within the population, although potentially only temporarily. This branching behaviour arises due to the emergence of a negative feedback with the maximum infected density on a cycle, which is strongest when the infected population is large. This work reinforces the qualitative differences between tolerance and resistance evolution, but also provides theoretical evidence for the theory that heterogeneous environments promote host-parasite diversity, hence constant environment assumptions may omit important evolutionary outcomes.

Transmission, relatedness, and the evolution of cooperative symbionts.

Cooperative interactions between species, termed mutualisms, play a key role in shaping natural ecosystems, economically important agricultural systems, and in influencing human health. Across different mutualisms, there is significant variation in the benefit that hosts receive from their symbionts. Empirical data suggest that transmission mode can help explain this variation: vertical transmission, where symbionts infect their host's offspring, leads to symbionts that provide greater benefits to their hosts than horizontal transmission, where symbionts leave their host and infect other hosts in the population. However, two different theoretical explanations have been given for this pattern: firstly, vertical transmission aligns the fitness interests of hosts and their symbionts; secondly, vertical transmission leads to increased relatedness between symbionts sharing a host, favouring cooperation between symbionts. We used a combination of analytical models and dynamic simulations to tease these factors apart, in order to compare their separate influences and see how they interact. We found that relatedness between symbionts sharing a host, rather than transmission mode per se, was the most important factor driving symbiont cooperation. Transmission mode mattered mainly because it determined relatedness. We also found evolutionary branching throughout much of our simulation, suggesting that a combination of transmission mode and multiplicity of infections could lead to the stable coexistence of different symbiont strategies.

Coevolution of cannibalistic predators and timid prey: evolutionary cycling and branching.

We investigate the coevolution of cannibalistic predators and timid prey, which seek refuge upon detecting a predator. To understand how the species affect each other's evolution, we derived the ecological model from individual-level processes using ordinary differential equations. The ecological dynamics exhibit bistability between equilibrium and periodic attractors, which may disappear through catastrophic bifurcations. Using the critical function analysis of adaptive dynamics, we classify general trade-offs between cannibalism and prey capture that produce different evolutionary outcomes. The evolutionary analysis reveals several ways in which cannibalism emerges as a response to timidity of the prey. The long-term coevolution either attains a singularity, or becomes cyclic through two mechanisms: genetical cycles through Hopf bifurcation of the singularity, or ecogenetical cycles involving abrupt switching between ecological attractors. Further diversification of cannibalism occurs through evolutionary branching, which is predicted to be delayed when simultaneous prey evolution is necessary for the singularity's attainability. We conclude that predator-prey coevolution produces a variety of outcomes, in which evolutionary cycles are commonplace.

Spatial heterogeneity and evolution of fecundity-affecting traits.

It is widely recognized that spatial structure in a population has some, and occasionally great, impacts on ecological and evolutionary dynamics. However, it has been observed that in the homogeneous Wright's island model with a certain standard demographic assumption, spatial structure does not affect the fitness gradient of a fecundity-affecting trait. The location and convergence stability of singular strategies thus remain unchanged. Furthermore, evolutionary branching is impossible for small dispersal rates, and for a wide class of fecundity functions, evolutionary branching is impossible for any dispersal rate if branching does not occur in the corresponding well-mixed model. Spatially homogeneous structure thus often inhibits evolutionary branching. Here we study the impact of spatial heterogeneity on evolutionary dynamics. We consider an infinite Wright's island model, where different islands have different capacity and fecundity consequences, and therefore the population is spatially heterogeneous. Through the analysis of metapopulation fitness, we derive its first-order and second-order derivatives with respect to mutant's trait, which are explicitly represented in terms of fecundity derivatives. The selection gradient turns out to be a biased average of local selection pressures in different patch types. We find that evolutionary branching is generally favored in the presence of spatial heterogeneity. We also find a simple condition under which evolutionary branching is particularly favored. Applications to public-goods cooperation and emergent evolutionary branching to cooperators and defectors are discussed.

Evolution of mate-finding Allee effect in prey.

The search for mates is often accompanied with conspicuous behaviour or morphology that can be exploited by predators. Here we explore the evolutionary consequences of a trade-off that arises naturally between mate acquisition and risk of predation and study evolution of the rate at which male prey search for mates in a population subject to a mate-finding Allee effect and exposed to either generalist or specialist predators. Since we show that the mate search rate determines the strength of the mate-finding Allee effect, we can alternatively view this as evolution of the mate-finding Allee effect in prey. We contrast two different life histories and find that, predominantly, male prey either evolve towards the maximal mate search rate yielding the weakest possible mate-finding Allee effect (thus showing no adaptive response in mating behaviour to predation risk) or evolutionary bi-stability occurs. In the latter case, males evolve a relatively low mate search rate (hence a relatively strong mate-finding Allee effect, interpreted as an adaptive response of male prey to predation) when initially slow or the maximal mate search rate when initially fast. Disruptive selection does not occur in populations exposed to generalist predators but is possible when predators are specialists. The dimorphic phase, in which fast and conspicuous male prey coexist with slow and cryptic ones, is however but a transient in evolutionary dynamics as one branch goes extinct while the other evolves towards the maximal mate search rate.

The Implications of Eco-Evolutionary Processes for the Emergence of Marine Plankton Community Biogeography.

Models of community assembly have been used to illustrate how the many functionally diverse species that compose plankton food webs can coexist. However, the evolutionary processes leading to the emergence of plankton food webs and their interplay with migratory processes and spatial heterogeneity are yet to be explored. We study the eco-evolutionary dynamics of a modeled plankton community structured in both size and space and physiologically constrained by empirical data. We demonstrate that a complex yet ecologically and evolutionarily stable size-structured food web can emerge from an initial set of two monomorphic phytoplankton and zooplankton populations. We also show that the coupling of spatial heterogeneity and migration results in the emergence of specific biogeographic patterns: (i) the emergence of a source-sink structure of the plankton metacommunities, (ii) changes in size diversity dependent on migratory intensity and on the scale at which diversity is considered (local vs. global), and (iii) the emergence of eco-evolutionary provinces (i.e., a spatial unit characterized by some level of abiotic heterogeneity but of homogenous size composition due to horizontal movements) at spatial scales that increase with the strength of the migratory processes.