Dynamics of an age-structured population with Allee effects and harvesting

We propose a discrete-time, age-structured population model to study the impact of Allee effects and harvesting. It is assumed that survival probabilities from one age class to the next are constants and fertility rate is a function of weighted total population size. Global extinction is certain if the maximal growth rate of the population is less than one. The model can have multiple attractors and the asymptotic dynamics of the population depend on its initial distribution if the maximal growth rate is larger than one. An Allee threshold depending on the components of the unstable interior equilibrium is derived when only the last age class can reproduce. The population becomes extinct if its initial population distribution is below the threshold. Harvesting on any particular age class can decrease the magnitude of the possible stable interior equilibrium and increase the magnitude of the unstable interior equilibrium simultaneously.     

Dynamics of an age-structured population with Allee effects and harvesting

We propose a discrete-time, age-structured population model to study the impact of Allee effects and harvesting. It is assumed that survival probabilities from one age class to the next are constants and fertility rate is a function of weighted total population size. Global extinction is certain if the maximal growth rate of the population is less than one. The model can have multiple attractors and the asymptotic dynamics of the population depend on its initial distribution if the maximal growth rate is larger than one. An Allee threshold depending on the components of the unstable interior equilibrium is derived when only the last age class can reproduce. The population becomes extinct if its initial population distribution is below the threshold. Harvesting on any particular age class can decrease the magnitude of the possible stable interior equilibrium and increase the magnitude of the unstable interior equilibrium simultaneously.     

Allee effects,extinctions, and chaotic transients in simple population models

Discrete time single species models with overcompensating density dependence and an Allee effect due to predator satiation and mating limitation are investigated. The models exhibit four behaviors: persistence for all initial population densities, bistability in which a population persists for intermediate initial densities and otherwise goes extinct, extinction for all initial densities, and essential extinction in which "almost every" initial density leads to extinction. For fast-growing populations, these models show populations can persist at high levels of predation even though lower levels of predation lead to essential extinction. Alternatively, increasing the predator's handling time, the population's carrying capacity, or the likelihood of mating success may lead to essential extinction. In each of these cases, the mechanism behind these disappearances are chaotic dynamics driving populations below a critical threshold determined by the Allee effect. These disappearances are proceeded by chaotic transients that are proven to be approximately exponentially distributed in length and highly sensitive to initial population densities.     

Allee effects can both conserve and create spatial heterogeneity in population densities

In order to determine conditions which allow the Allee effect (caused by biparental reproduction) to conserve and create spatial heterogeneity in population densities, we studied a deterministic model of a symmetric two-patch metapopulation. We proved that under certain conditions there exist stable equilibria with unequal population densities in the two patches, a situation which can be interpreted as conserved heterogeneity. Furthermore, the Allee effect can lead to instability of the equilibrium with equal population densities if some degree of competition is assumed to occur between the subpopulations (non-local competition). This indicates the potential of the Allee effect to create spatial heterogeneity. Neither of these effects appear under biologically realistic parameter values in a model where uniparental reproduction is assumed. We proved that both the between-patch migration intensity and the degree of non-local competition are decisive in determining boundaries between these types of behaviour of the spatial system with Allee effect. Therefore, we propose that the Allee effect, migration intensity, and non-local competition should be considered jointly in studies focusing on problems like pattern formation in space and invasions of spreading species.     

Evolutionary dynamics and strong Allee effects

We describe the dynamics of an evolutionary model for a population subject to a strong Allee effect. The model assumes that the carrying capacity k(u), inherent growth rate r(u), and Allee threshold a(u) are functions of a mean phenotypic trait u subject to evolution. The model is a plane autonomous system that describes the coupled population and mean trait dynamics. We show bounded orbits equilibrate and that the Allee basin shrinks (and can even disappear) as a result of evolution. We also show that stable non-extinction equilibria occur at the local maxima of k(u) and that stable extinction equilibria occur at local minima of r(u). We give examples that illustrate these results and demonstrate other consequences of an Allee threshold in an evolutionary setting. These include the existence of multiple evolutionarily stable, non-extinction equilibria, and the possibility of evolving to a non-evolutionary stable strategy (ESS) trait from an initial trait near an ESS.     

Evolutionary dynamics and strong Allee effects

We describe the dynamics of an evolutionary model for a population subject to a strong Allee effect. The model assumes that the carrying capacity k(u), inherent growth rate r(u), and Allee threshold a(u) are functions of a mean phenotypic trait u subject to evolution. The model is a plane autonomous system that describes the coupled population and mean trait dynamics. We show bounded orbits equilibrate and that the Allee basin shrinks (and can even disappear) as a result of evolution. We also show that stable non-extinction equilibria occur at the local maxima of k(u) and that stable extinction equilibria occur at local minima of r(u). We give examples that illustrate these results and demonstrate other consequences of an Allee threshold in an evolutionary setting. These include the existence of multiple evolutionarily stable, non-extinction equilibria, and the possibility of evolving to a non-evolutionary stable strategy (ESS) trait from an initial trait near an ESS.     

General Allee effect in two-species population biology

The main objective of this work is to present a general framework for the notion of the strong Allee effect in population models, including competition, mutualistic, and predator–prey models. The study is restricted to the strong Allee effect caused by an inter-specific interaction. The main feature of the strong Allee effect is that the extinction equilibrium is an attractor. We show how a ‘phase space core’ of three or four equilibria is sufficient to describe the essential dynamics of the interaction between two species that are prone to the Allee effect. We will introduce the notion of semistability in planar systems. Finally, we show how the presence of semistable equilibria increases the number of possible Allee effect cores.     

Allee effects in stochastic populations

The Allee effect, or inverse density dependence at low population sizes, could seriously impact preservation and management of biological populations. The mounting evidence for widespread Allee effects has lately inspired theoretical studies of how Allee effects alter population dynamics. However, the recent mathematical models of Allee effects have been missing another important force prevalent at low population sizes: stochasticity. In this paper, the combination of Allee effects and stochasticity is studied using diffusion processes, a type of general stochastic population model that accommodates both demographic and environmental stochastic fluctuations. Including an Allee effect in a conventional deterministic population model typically produces an unstable equilibrium at a low population size, a critical population level below which extinction is certain. In a stochastic version of such a model, the probability of reaching a lower size a before reaching an upper size b , when considered as a function of initial population size, has an inflection point at the underlying deterministic unstable equilibrium. The inflection point represents a threshold in the probabilistic prospects for the population and is independent of the type of stochastic fluctuations in the model. In particular, models containing demographic noise alone (absent Allee effects) do not display this threshold behavior, even though demographic noise is considered an "extinction vortex". The results in this paper provide a new understanding of the interplay of stochastic and deterministic forces in ecological populations.     

General Allee effect in two-species population biology

The main objective of this work is to present a general framework for the notion of the strong Allee effect in population models, including competition, mutualistic, and predator-prey models. The study is restricted to the strong Allee effect caused by an inter-specific interaction. The main feature of the strong Allee effect is that the extinction equilibrium is an attractor. We show how a 'phase space core' of three or four equilibria is sufficient to describe the essential dynamics of the interaction between two species that are prone to the Allee effect. We will introduce the notion of semistability in planar systems. Finally, we show how the presence of semistable equilibria increases the number of possible Allee effect cores.     

Allee effects and resilience in stochastic populations

Allee effects, or positive functional relationships between a population’s density (or size) and its per unit abundance growth rate, are now considered to be a widespread if not common influence on the growth of ecological populations. Here we analyze how stochasticity and Allee effects combine to impact population persistence. We compare the deterministic and stochastic properties of four models: a logistic model (without Allee effects), and three versions of the original model of Allee effects proposed by Vito Volterra representing a weak Allee effect, a strong Allee effect, and a strong Allee effect with immigration. We employ the diffusion process approach for modeling single-species populations, and we focus on the properties of stationary distributions and of the mean first passage times. We show that stochasticity amplifies the risks arising from Allee effects, mainly by prolonging the amount of time a population spends at low abundance levels. Even weak Allee effects become consequential when the ubiquitous stochastic forces affecting natural populations are accounted for in population models. Although current concepts of ecological resilience are bound up in the properties of deterministic basins of attraction, a complete understanding of alternative stable states in ecological systems must include stochasticity.     

Combined impacts of Allee effects and parasitism

Despite their individual importance for population dynamics and conservation biology, the combined impacts of Allee effects and parasitism have received little attention. We built a mathematical model to compare the dynamics of populations with or without Allee effects when infected by microparasites. We show that the influence of an Allee effect takes the form of a tradeoff. The presence of an Allee effect in host populations may protect them, by reducing the range of population sizes that allow parasite spread. Yet if infection spreads, the Allee effect weakens host populations by reducing their size and by widening the range of parasite species that lead them to extinction. These results have important implications for predicting the survival of threatened populations or the success of reintroductions, and may help define size ranges within which given populations should be maintained to prevent both epidemics and Allee effects driven extinctions.     

How predator functional responses and Allee effects in prey affect the paradox of enrichment and population collapses

In Rosenzweig-MacArthur models of predator-prey dynamics, Allee effects in prey usually destabilize interior equilibria and can suppress or enhance limit cycles typical of the paradox of enrichment. We re-evaluate these conclusions through a complete classification of a wide range of Allee effects in prey and predator's functional response shapes. We show that abrupt and deterministic system collapses not preceded by fluctuating predator-prey dynamics occur for sufficiently steep type III functional responses and strong Allee effects (with unstable lower equilibrium in prey dynamics). This phenomenon arises as type III functional responses greatly reduce cyclic dynamics and strong Allee effects promote deterministic collapses. These collapses occur with decreasing predator mortality and/or increasing susceptibility of the prey to fall below the threshold Allee density (e.g. due to increased carrying capacity or the Allee threshold itself). On the other hand, weak Allee effects (without unstable equilibrium in prey dynamics) enlarge the range of carrying capacities for which the cycles occur if predators exhibit decelerating functional responses. We discuss the results in the light of conservation strategies, eradication of alien species, and successful introduction of biocontrol agents.     

Incorporating Allee effects into reintroduction strategies

Allee effects, the reduction of vital rates at low population densities, can occur through several mechanisms, all of which potentially apply to reintroduced populations. Reintroduced populations are initially at low densities, hence Allee effects can potentially lead to reintroduction failure despite habitat quality being sufficient to allow long-term persistence if the population survived the establishment phase. The probability of such failures can potentially be reduced by releasing large numbers of organisms, by reducing post-release dispersal or mortality through management, or by directly managing the Allee effects, e.g., by implementing predator control or food supplementation until population size increases. However, such measures incur costs, as large releases have a greater impact on source populations, and management actions require financial and other resources. It is therefore essential to compare the costs and benefits of attempting to reduce Allee effects in reintroduction programs. Here we advocate the use of structured decision-making frameworks whereby alternative strategies are nominated, probability distributions of outcomes obtained under different strategies, and utilities assigned to different outcomes. We illustrate the potential application of such decision frameworks using projections from a stochastic population model including Allee effects. As there will seldom be estimates of Allee effects available from the species or system involved, it will be necessary to predict these effects based on the biology of the species and data from other systems. In doing so, it is important to identify mechanisms for proposed Allee effects, and to avoid misleading inferences from correlations subject to confounds. In particular, naive interpretations of correlations between numbers released and reintroduction success may exaggerate the benefits of releasing large numbers.     

集合种群的Allee效应研究进展

随着全球环境破坏的加剧,物种丧失的速度加快,人们日益关注生物多样性的保护。种群生物学和自然保护生物学的一些研究表明,如果一个局域种群受到Allee效应的影响,最终可能走向灭绝。从物种保护的角度考虑,分别介绍了集合种群水平上的Allee效应的和似Allee效应,比较了集合种群的Allee效应和似Allee效应产生的原因,以及集合种群的Allee效应和局域种群的Allee效应之间的关系、集合种群的似Allee效应和局域种群的Allee效应之间的关系,并提出集合种群的Allee效应还需要进一步的研究。     

Allee effects and extinction in a lattice model

In the interest of conservation, the importance of having a large habitat available for a species is widely known. Here, we introduce a lattice-based model for a population and look at the importance of fluctuations as well as that of the population density, particularly with respect to Allee effects. We examine the model analytically and by Monte Carlo simulations and find that, while the size of the habitat is important, there exists a critical population density below which the probability of extinction is greatly increased. This has large consequences with respect to conservation, especially in the design of habitats and for populations whose density has become small. In particular, we find that the probability of survival for small populations can be increased by a reduction in the size of the habitat and show that there exists an optimal size reduction.     

Integrodifference equations, Allee effects, and invasions

 Models that describe the spread of invading organisms often assume no Allee effect. In contrast, abundant observational data provide evidence for Allee effects. We study an invasion model based on an integrodifference equation with an Allee effect. We derive a general result for the sign of the speed of invasion. We then examine a special, linear–constant, Allee function and introduce a numerical scheme that allows us to estimate the speed of traveling wave solutions. Received: 14 April 2000 / Revised version: 23 December 2000 / Published online: 8 February 2002     

Fatal disease and demographic Allee effect: population persistence and extinction

If a healthy stable host population at the disease-free equilibrium is subject to the Allee effect, can a small number of infected individuals with a fatal disease cause the host population to go extinct? That is, does the Allee effect matter at high densities? To answer this question, we use a susceptible–infected epidemic model to obtain model parameters that lead to host population persistence (with or without infected individuals) and to host extinction. We prove that the presence of an Allee effect in host demographics matters even at large population densities. We show that a small perturbation to the disease-free equilibrium can eventually lead to host population extinction. In addition, we prove that additional deaths due to a fatal infectious disease effectively increase the Allee threshold of the host population demographics.