Population dynamics in a time-varying environment with fat-tailed correlations.

Temporal environmental noise (EN) is a prevalent natural phenomenon that controls population and community dynamics, shaping the destiny of biological species and genetic types. Conventional theoretical models often depict EN as a Markovian process with an exponential distribution of correlation times, resulting in two distinct qualitative dynamical categories: quenched (long environmental timescales) and annealed (short environmental timescales). However, numerous empirical studies demonstrate a fat-tailed decay of correlation times.

Processes governing species richness in communities exposed to temporal environmental stochasticity: A review and synthesis of modelling approaches.

Research into the processes governing species richness has often assumed that the environment is fixed, whereas realistic environments are often characterised by random fluctuations over time. This temporal environmental stochasticity (TES) changes the demographic rates of species populations, with cascading effects on community dynamics and species richness. Theoretical and applied studies have used process-based mathematical models to determine how TES affects species richness, but under a variety of frameworks.

Extinction time distributions of populations and genotypes.

Ultimately, the eventual extinction of any biological population is an inevitable outcome. While extensive research has focused on the average time it takes for a population to go extinct under various circumstances, there has been limited exploration of the distributions of extinction times and the likelihood of significant fluctuations. Recently, Hathcock and Strogatz [D.

Quantitative Characteristics of Stabilizing and Equalizing Mechanisms.

AbstractAn understanding of the mechanisms that facilitate coexistence in ecological communities poses a major challenge to theoretical ecology. A popular paradigmatic scheme distinguishes between two qualitatively different processes that help species to coexist: stabilizing mechanisms increase niche differentiation, making the intraspecific competition stronger than the interspecific one, while equalizing mechanisms diminish fitness differences, making the competition less decisive. Here, we provide an analytic and numeric examination of the quantitative features associated with this scheme for a simple, two-species competition model.

Evolution in fluctuating environments: A generic modular approach.

Evolutionary processes take place in fluctuating environments, where carrying capacities and selective forces vary over time. The fate of a mutant type and the persistence time of polymorphic states were studied in some specific cases of varying environments, but a generic methodology is still lacking. Here, we present such a general analytic framework.

Quantifying invasibility.

Invasibility, the chance of a population to grow from rarity and become established, plays a fundamental role in population genetics, ecology, epidemiology and evolution. For many decades, the mean growth rate of a species when it is rare has been employed as an invasion criterion. Recent studies show that the mean growth rate fails as a quantitative metric for invasibility, with its magnitude sometimes even increasing while the invasibility decreases.

How the storage effect and the number of temporal niches affect biodiversity in stochastic and seasonal environments.

Temporal environmental variations affect diversity in communities of competing populations. In particular, the covariance between competition and environment is known to facilitate invasions of rare species via the storage effect. Here we present a quantitative study of the effects of temporal variations in two-species and in diverse communities.

How temporal environmental stochasticity affects species richness: Destabilization, neutralization and the storage effect.

Temporal environmental stochasticity (TES), along with the variations of demographic rates associated with it, is ubiquitous in nature. Here we study the effect of TES on the species richness of diverse communities. In such communities the biodiversity at equilibrium reflects the balance between the rate at which new types are added (via migration, mutation or speciation) and the rate of extinction.

Competition with abundance-dependent fitness and the dynamics of heterogeneous populations in fluctuating environment.

Species competition takes place in a fluctuating environment, so the selective forces on different populations vary through time. In many realistic situations the mean fitness and the amplitude of its temporal variations are abundance-dependent. Here we present a theory of two-species competition with abundance-dependent stochastic fitness variations and solve for the chance of ultimate fixation, the time to absorption and the time to fixation.

Alternative States in Plant Communities Driven by a Life-History Trade-Off and Demographic Stochasticity.

AbstractLife-history trade-offs among species are major drivers of community assembly. Most studies investigate how trade-offs promote deterministic coexistence of species. It remains unclear how trade-offs may instead promote historically contingent exclusion of species, where species dominance is affected by initial abundances, causing alternative community states via priority effects.

Taming the diffusion approximation through a controlling-factor WKB method.

The diffusion approximation (DA) is widely used in the analysis of stochastic population dynamics, from population genetics to ecology and evolution. The DA is an uncontrolled approximation that assumes the smoothness of the calculated quantity over the relevant state space and fails when this property is not satisfied. This failure becomes severe in situations where the direction of selection switches sign.

Intraspecific variability in fluctuating environments: mechanisms of impact on species diversity.

Recent studies have found considerable trait variations within species. The effect of such intraspecific trait variability (ITV) on the stability, coexistence, and diversity of ecological communities received considerable attention and in many models it was shown to impede coexistence and decrease species diversity. Here we present a numerical study of the effect of genetically inherited ITV on species persistence and diversity in a temporally fluctuating environment.

Invasion growth rate and its relevance to persistence: a response to Technical Comment by Ellner et al.

Ellner et al. (2020) state that identifying the mechanisms producing positive invasion growth rates (IGR) is useful in characterising species persistence. We agree about the importance of the sign of IGR as a binary indicator of persistence, but question whether its magnitude provides much information once the sign is given.

Stochasticity-induced stabilization in ecology and evolution: a new synthesis.

The ability of random environmental variation to stabilize competitor coexistence was pointed out long ago and, in recent years, has received considerable attention. Analyses have focused on variations in the log abundances of species, with mean logarithmic growth rates when rare, , used as metrics for persistence. However, invasion probabilities and the times to extinction are not single-valued functions of and, in some cases, decrease as increases.

Mean growth rate when rare is not a reliable metric for persistence of species.

The coexistence of many species within ecological communities poses a long-standing theoretical puzzle. Modern coexistence theory (MCT) and related techniques explore this phenomenon by examining the chance of a species population growing from rarity in the presence of all other species. The mean growth rate when rare, , is used in MCT as a metric that measures persistence properties (like invasibility or time to extinction) of a population.

Comprehensive phase diagram for logistic populations in fluctuating environment.

Population dynamics reflects an underlying birth-death process, where the rates associated with different events may depend on external environmental conditions and on the population density. A whole family of simple and popular deterministic models (such as logistic growth) supports a transcritical bifurcation point between an extinction phase and an active phase. Here we provide a comprehensive analysis of the phases of that system, taking into account both the endogenous demographic noise (random birth and death events) and the effect of environmental stochasticity that causes variations in birth and death rates.

Phase Diagram for Logistic Systems under Bounded Stochasticity.

Extinction is the ultimate absorbing state of any stochastic birth-death process; hence, the time to extinction is an important characteristic of any natural population. Here we consider logistic and logisticlike systems under the combined effect of demographic and bounded environmental stochasticity. Three phases are identified: an inactive phase where the mean time to extinction T increases logarithmically with the initial population size, an active phase where T grows exponentially with the carrying capacity N, and a temporal Griffiths phase, with a power-law relationship between T and N.

Simulation of spatial systems with demographic noise.

The demographic (shot) noise in population dynamics scales with the square root of the population size. This process is very important, as it yields an absorbing state at zero field, but simulating it, especially on spatial domains, is a nontrivial task. Here, we analyze two similar methods that were suggested for simulating the corresponding Langevin equation, one by Pechenik and Levine and the other by Dornic, Chaté, and Muñoz (DCM).

Noise-induced stabilization and fixation in fluctuating environment.

The dynamics of a two-species community of N competing individuals are considered, with an emphasis on the role of environmental variations that affect coherently the fitness of entire populations. The chance of fixation of a mutant (or invading) population is calculated as a function of its mean relative fitness, the amplitude of fitness variations and their typical duration. We emphasize the distinction between the case of pairwise competition and the case of global competition; in the latter a noise-induced stabilization mechanism yields a higher chance of fixation for a single mutant.

Theory of time-averaged neutral dynamics with environmental stochasticity.

Competition is the main driver of population dynamics, which shapes the genetic composition of populations and the assembly of ecological communities. Neutral models assume that all the individuals are equivalent and that the dynamics is governed by demographic (shot) noise, with a steady state species abundance distribution (SAD) that reflects a mutation-extinction equilibrium. Recently, many empirical and theoretical studies emphasized the importance of environmental variations that affect coherently the relative fitness of entire populations.

Alternative steady states in ecological networks.

In many natural situations, one observes a local system with many competing species that is coupled by weak immigration to a regional species pool. The dynamics of such a system is dominated by its stable and uninvadable (SU) states. When the competition matrix is random, the number of SUs depends on the average value and variance of its entries.

Fixation and absorption in a fluctuating environment.

A fundamental problem in the fields of population genetics, evolution, and community ecology, is the fate of a single mutant, or invader, introduced in a finite population of wild types. For a fixed-size community of N individuals, with Markovian, zero-sum dynamics driven by stochastic birth-death events, the mutant population eventually reaches either fixation or extinction. The classical analysis, provided by Kimura and his coworkers, is focused on the neutral case, [where the dynamics is only due to demographic stochasticity (drift)], and on time-independent selective forces (deleterious/beneficial mutation).

Empirical analysis of vegetation dynamics and the possibility of a catastrophic desertification transition.

The process of desertification in the semi-arid climatic zone is considered by many as a catastrophic regime shift, since the positive feedback of vegetation density on growth rates yields a system that admits alternative steady states. Some support to this idea comes from the analysis of static patterns, where peaks of the vegetation density histogram were associated with these alternative states. Here we present a large-scale empirical study of vegetation dynamics, aimed at identifying and quantifying directly the effects of positive feedback.

Stability of two-species communities: Drift, environmental stochasticity, storage effect and selection.

The dynamics of two competing species in a finite size community is one of the most studied problems in population genetics and community ecology. Stochastic fluctuations lead, inevitably, to the extinction of one of the species, but the relevant timescale depends on the underlying dynamics. The persistence time of the community has been calculated both for neutral models, where the only driving force of the system is drift (demographic stochasticity), and for models with strong selection.

Solution of the spatial neutral model yields new bounds on the Amazonian species richness.

Neutral models, in which individual agents with equal fitness undergo a birth-death-mutation process, are very popular in population genetics and community ecology. Usually these models are applied to populations and communities with spatial structure, but the analytic results presented so far are limited to well-mixed or mainland-island scenarios. Here we combine analytic results and numerics to obtain an approximate solution for the species abundance distribution and the species richness for the neutral model on continuous landscape.