Speeds of invasion in a model with strong or weak Allee effects

We study an invasion model based on a reaction-diffusion equation with an Allee effect. We use a special, piecewise-linear, population growth rate. This function allows us to obtain traveling wave solutions and to compute wave speeds for a full range of Allee effects, including weak Allee effects. Some investigators claim that linearization fails to give the correct speed of invasion if there is an Allee effect. We show that the minimum speed for a sufficiently weak Allee may, in fact, be the same as that derived by means of linearization.     

Allee threshold and extinction threshold for spatially explicit metapopulation dynamics with Allee effects

In this paper, we investigate a spatially explicit metapopulation model with Allee effects. We refer to the patch occupancy model introduced by Levins (Bull Entomol Soc Am 15:237–240, 1969) as a spatially implicit metapopulation model, i.e., each local patch is either occupied or vacant and a vacant patch can be recolonized by a randomly chosen occupied patch from anywhere in the metapopulation. When we transform the model into a spatially explicit one by using a lattice model, the obtained model becomes theoretically equivalent to a “lattice logistic model” or a “basic contact process”. One of the most popular or standard metapopulation models with Allee effects, developed by Amarasekare (Am Nat 152:298–302, 1998), supposes that those effects are introduced formally by means of a logistic equation. However, it is easier to understand the ecological meaning of associating Allee effects with this model if we suppose that only the logistic colonization term directly suffers from Allee effects. The resulting model is also well defined, and therefore we can naturally examine it by Monte Carlo simulation and by doublet and triplet decoupling approximation. We then obtain the following specific features of one-dimensional lattice space: (1) the metapopulation as a whole does not have an Allee threshold for initial population size even when each local population follows the Allee effects; and (2) a metapopulation goes extinct when the extinction rate of a local population is lower than that in the spatially implicit model. The real ecological metapopulation lies between two extremes: completely mixing interactions between patches on the one hand and, on the other, nearest neighboring interactions with only two nearest neighbors. Thus, it is important to identify the metapopulation structure when we consider the problems of invasion species such as establishment or the speed of expansion.     

The role of Allee effects in gypsy moth, <Emphasis Type="Italic">Lymantria dispar</Emphasis> (L.), invasions

Allee effects have been applied historically in efforts to understand the low-density population dynamics of rare and endangered species. Many biological invasions likewise experience the phenomenon of decreasing population growth rates at low population densities because most founding populations of introduced nonnative species occur at low densities. In range expansion of established species, the initial colonizers of habitat beyond the organism’s current range are usually at low density, and thus could be subject to Allee dynamics. There has been consistent empirical and theoretical evidence demonstrating, and in some cases quantifying, the role of Allee dynamics in the gypsy moth, Lymantria dispar (L.), invasion of North America. In this review, we examine the potential causes of the Allee effect in the gypsy moth and highlight the importance of mate-finding failure as a primary mechanism behind an Allee effect, while the degree to which generalist predators induce an Allee effect remains unclear. We then explore the role of Allee effects in the establishment and spread dynamics of the gypsy moth system, which conceptually could serve as a model system for understanding how Allee effects manifest themselves in the dynamics of biological invasions.     

Invasion dynamics of epidemic with the Allee effect

Investigating the likely success of epidemic invasion is important in the epidemic management and control. In the present study, the invasion of epidemic is initially introduced to a predator-prey system, both species of which are considered to be subject to the Allee effect. Mathematically, the invasion dynamics is described by three nonlinear diffusion-reaction equations and the spatial implicit and explicit models are designed. By means of extensive numerical simulations, the results of spatial implicit model show that the Allee effect has an opposite impact on the invasion criteria and local dynamics when that on the different species. As the intensity of the Allee effect increases, the domain of epidemic invasion reduces and the system dynamics is changed from the stable state to the limit cycle and finally becomes the chaotic state when the susceptible prey with the Allee effect, but the domain expands and the system dynamics is changed from limit cycle to a table point when the predator is subject to the Allee effect. Results from the spatial explicit model show that the strong intensity of the Allee effect can lead to the catastrophic global extinction of all species in the case of that on the susceptible prey. While the predator with the Allee effect, the increased intensity of which makes spatial species reach a stable state. Furthermore, numerical simulations reveal a certain relationship between the invasion speed and spatial patterns.     

Allee effects, invasion pinning, and species' borders

All species' ranges are the result of successful past invasions. Thus, models of species' invasions and their failure can provide insight into the formation of a species' geographic range. Here, we study the properties of invasion models when a species cannot persist below a critical population density known as an "Allee threshold." In both spatially continuous reaction-diffusion models and spatially discrete coupled ordinary-differential-equation models, the Allee effect can cause an invasion to fail. In patchy landscapes (with dynamics described by the spatially discrete model), range limits caused by propagation failure (pinning) are stable over a wide range of parameters, whereas, in an uninterrupted habitat (with dynamics described by a spatially continuous model), the zero velocity solution is structurally unstable and thus unlikely to persist in nature. We derive conditions under which invasion waves are pinned in the discrete space model and discuss their implications for spatially complex dynamics, including critical phenomena, in ecological landscapes. Our results suggest caution when interpreting abrupt range limits as stemming either from competition between species or a hard environmental limit that cannot be crossed: under a wide range of plausible ecological conditions, species' ranges may be limited by an Allee effect. Several example systems appear to fit our general model.     

Modelling mate-finding Allee effects and populations dynamics,with applications in pest control

In this paper, we review how mate-finding Allee effects enter population dynamical models that consider both sexes, highlight possible limitations of the more widely used “one-sex” models, and outline the links between the different model classes. We further explore interactions between the mate-finding Allee effect and other mechanisms relevant to pest-control strategies: release of natural enemies, sterile male release, and culling. Many of these strategies impose an additional component Allee effect on the population, and we discuss which of them might be efficient in the control of pest species that also suffer from the failure to locate mates. We focus primarily on eradication thresholds; our simple models show that most of the strategies yield similar results, and depending on the costs, one strategy or a combination of several can lead to the most efficient control.     

Success rate of a biological invasion in terms of the spatial distribution of the founding population

We analyze the role of the spatial distribution of the initial condition in reaction–diffusion models of biological invasion. Our study shows that, in the presence of an Allee effect, the precise shape of the initial (or founding) population is of critical importance for successful invasion. Results are provided for one-dimensional and two-dimensional models. In the one-dimensional case, we consider initial conditions supported by two disjoint intervals of length L/2 and separated by a distance α. Analytical as well as numerical results indicate that the critical size L ^∗(α) of the population, where the invasion is successful if and only if L>L ^∗(α), is a continuous function of α and tends to increase with α, at least when α is not too small. This result emphasizes the detrimental effect of fragmentation. In the two-dimensional case, we consider more general, stochastically generated initial conditions u ₀, and we provide a new and rigorous definition of the rate of fragmentation of u ₀. We then conduct a statistical analysis of the probability of successful invasion depending on the size of the support of u ₀ and the fragmentation rate of u ₀. Our results show that the outcome of an invasion is almost completely determined by these two parameters. Moreover, we observe that the minimum abundance required for successful invasion tends to increase in a non-linear fashion with the fragmentation rate. This effect of fragmentation is enhanced as the strength of the Allee effect is increased.     

The evidence for Allee effects

Allee effects are an important dynamic phenomenon believed to be manifested in several population processes, notably extinction and invasion. Though widely cited in these contexts, the evidence for their strength and prevalence has not been critically evaluated. We review results from 91 studies on Allee effects in natural animal populations. We focus on empirical signatures that are used or might be used to detect Allee effects, the types of data in which Allee effects are evident, the empirical support for the occurrence of critical densities in natural populations, and differences among taxa both in the presence of Allee effects and primary causal mechanisms. We find that conclusive examples are known from Mollusca, Arthropoda, and Chordata, including three classes of vertebrates, and are most commonly documented to result from mate limitation in invertebrates and from predator–prey interactions in vertebrates. More than half of studies failed to distinguish component and demographic Allee effects in data, although the distinction is crucial to most of the population-level dynamic implications associated with Allee effects (e.g., the existence of an unstable critical density associated with strong Allee effects). Thus, although we find conclusive evidence for Allee effects due to a variety of mechanisms in natural populations of 59 animal species, we also find that existing data addressing the strength and commonness of Allee effects across species and populations is limited; evidence for a critical density for most populations is lacking. We suggest that current studies, mainly observational in nature, should be supplemented by population-scale experiments and approaches connecting component and demographic effects. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Population spread in patchy landscapes under a strong Allee effect

Many species of invasive insects establish and spread in regions around the world, causing enormous economical and environmental damage, in particular in forests. Some of these insects are subject to an Allee effect whereby the population must surpass a certain threshold in order to establish. Recent studies have examined the possibility of exploiting an Allee effect to improve existing control strategies. Forests and most other ecosystems show natural spatial variation, and human activities frequently increase the degree of spatial heterogeneity. It is therefore imperative to understand how the interplay between this spatial variation and individual movement behavior affects the overall speed of spread of an invasion. To this end, we study an integrodifference equation model in a patchy landscape and with Allee growth dynamics. Movement behavior of individuals varies according to landscape quality. Our study focuses on how the speed of the resulting traveling periodic wave depends on the interaction between landscape fragmentation, patch-dependent dispersal, and Allee population dynamics.     

Invasion speed is affected by geographical variation in the strength of Allee effects

Allee effects can play a critical role in slowing or preventing the establishment of low density founder populations of non-indigenous species. Similarly, the spread of established invaders into new habitats can be influenced by the degree to which small founder populations ahead of the invasion front are suppressed through Allee effects. We develop an approach to use empirical data on the gypsy moth, a non-indigenous invader in North America, to quantify the Allee threshold across geographical regions, and we report that the strength of the Allee effect is subject to spatial and temporal variability. Moreover, we present what is to our knowledge the first empirical evidence that geographical regions with higher Allee thresholds are associated with slower speeds of invasion.     

Evolution of dispersal traits along an invasion route in the wind‐dispersed Senecio inaequidens (Asteraceae)

In introduced organisms, dispersal propensity is expected to increase during range expansion. This prediction is based on the assumption that phenotypic plasticity is low compared to genetic diversity, and an increase in dispersal can be counteracted by the Allee effect. Empirical evidence in support of these hypotheses is however lacking. The present study tested for evidence of differentiation in dispersal‐related traits and the Allee effect in the wind‐dispersed invasive Senecio inaequidens (Asteraceae). We collected capitula from individuals in ten field populations, along an invasion route including the original introduction site in southern France. In addition, we conducted a common garden experiment from field‐collected seeds and obtained capitula from individuals representing the same ten field populations. We analysed phenotypic variation in dispersal traits between field and common garden environments as a function of the distance between populations and the introduction site. Our results revealed low levels of phenotypic differentiation among populations. However, significant clinal variation in dispersal traits was demonstrated in common garden plants representing the invasion route. In field populations, similar trends in dispersal‐related traits and evidence of an Allee effect were not detected. In part, our results supported expectations of increased dispersal capacity with range expansion, and emphasized the contribution of phenotypic plasticity under natural conditions.     

Allee Effects, Propagule Pressure and the Probability of Establishment: Risk Analysis for Biological Invasions

Colonization is of longstanding interest in theoretical ecology and biogeography, and in the management of weeds and other invasive species, including insect pests and emerging infectious diseases. Due to accelerating invasion rates and widespread economic costs and environmental damages caused by invasive species, colonization theory has lately become a matter of considerable interest. Here we review the concept of propagule pressure to inquire if colonization theory might provide quantitative tools for risk assessment of biological invasions. By formalizing the concept of propagule pressure in terms of stochastic differential equation models of population growth, we seek a synthesis of invasion biology and theoretical population biology. We focus on two components of propagule pressure that affect the chance of invasion: (1) the number of individuals initially introduced, and (2) the rate of subsequent immigration. We also examine how Allee effects, which are expected to be common in newly introduced populations, may inhibit establishment of introduced propagules. We find that the establishment curve (i.e., the chance of invasion as a function of initial population size), can take a variety of shapes depending on immigration rate, carrying capacity, and the severity of Allee effects. Additionally, Allee effects can cause the stationary distribution of population sizes to be bimodal, which we suggest is a possible explanation for time lags commonly observed between the detection of an introduced population and widespread invasion of the landscape.     

Critical patch size generated by Allee effect in gypsy moth, Lymantria dispar (L.)

Allee effects are important dynamical mechanisms in small-density populations in which per capita population growth rate increases with density. When positive density dependence is sufficiently severe (a 'strong' Allee effect), a critical density arises below which populations do not persist. For spatially distributed populations subject to dispersal, theory predicts that the occupied area also exhibits a critical threshold for population persistence, but this result has not been confirmed in nature. We tested this prediction in patterns of population persistence across the invasion front of the European gypsy moth (Lymantria dispar) in the United States in data collected between 1996 and 2008. Our analysis consistently provided evidence for effects of both population area and density on persistence, as predicted by the general theory, and confirmed here using a mechanistic model developed for the gypsy moth system. We believe this study to be the first empirical documentation of critical patch size induced by an Allee effect.     

Dangerously few liaisons: a review of mate-finding Allee effects

In this paper, we review mate-finding Allee effects from ecological and evolutionary points of view. We define ‘mate-finding’ as mate searching in mobile animals, and also as the meeting of gametes for sessile animals and plants (pollination). We consider related issues such as mate quality and choice, sperm limitation and physiological stimulation of reproduction by conspecifics, as well as discussing the role of demographic stochasticity in generating mate-finding Allee effects. We consider the role of component Allee effects due to mate-finding in generating demographic Allee effects (at the population level). Compelling evidence for demographic Allee effects due to mate-finding (as well as via other mechanisms) is still limited, due to difficulties in censusing rare populations or a failure to identify underlying mechanisms, but also because of fitness trade-offs, population spatial structure and metapopulation dynamics, and because the strength of component Allee effects may vary in time and space. Mate-finding Allee effects act on individual fitness and are thus susceptible to change via natural selection. We believe it is useful to distinguish two routes by which evolution can act to mitigate mate-finding Allee effects. The first is evolution of characteristics such as calls, pheromones, hermaphroditism, etc. which make mate-finding more efficient at low density, thus eliminating the Allee effect. Such adaptations are very abundant in the natural world, and may have arisen to avoid Allee effects, although other hypotheses are also possible. The second route is to avoid low density via adaptations such as permanent or periodic aggregation. In this case, the Allee effect is still present, but its effects are avoided. These two strategies may have different consequences in a world where many populations are being artificially reduced to low density: in the first case, population growth rate can be maintained, while in the second case, the mechanism to avoid Allee effects has been destroyed. It is therefore in these latter populations that we predict the greatest evidence for mate-finding Allee effects and associated demographic consequences. This idea is supported by the existing empirical evidence for demographic Allee effects. Given a strong effect that mate-finding appears to have on individual fitness, we support the continuing quest to find connections between component mate-finding Allee effects (individual reproductive fitness) and the demographic consequences. There are many reasons why such studies are difficult, but it is important, particularly given the increasing number of populations and species of conservation concern, that the ecological community understands more about how widespread demographic Allee effects really are, and why.     

Drug-resistant parasites and aggregated infection – early-season dynamics

We investigate the effect of spatial aggregation in the infection dynamics of nematode parasites in ruminants. We show that a high degree of spatial aggregation is likely to lead to a dramatically enhanced rate of invasion by drug-resistant strains. Received: 13 December 1999 / Revised version: 3 April 2000 / Published online: 4 October 2000     

Allee Effect and Control of Lake System Invasion

We consider the model of invasion prevention in a system of lakes that are connected via traffic of recreational boats. It is shown that in presence of an Allee effect, the general optimal control problem can be reduced to a significantly simpler stationary optimization problem of optimal invasion stopping. We consider possible values of model parameters for zebra mussels. The general N-lake control problem has to be solved numerically, and we show a number of typical features of solutions: distribution of control efforts in space and optimal stopping configurations related with the clusters in lake connection structure.     

Can a barrier zone stop invasion of a population?

Journal of Mathematical Biology - We consider an integro-difference model to study the effect of a stationary barrier zone on invasion of a population with a strong Allee effect. It is assumed that...     

Establishing a beachhead: a stochastic population model with an Allee effect applied to species invasion

We formulated a spatially explicit stochastic population model with an Allee effect in order to explore how invasive species may become established. In our model, we varied the degree of migration between local populations and used an Allee effect with variable birth and death rates. Because of the stochastic component, population sizes below the Allee effect threshold may still have a positive probability for successful invasion. The larger the network of populations, the greater the probability of an invasion occurring when initial population sizes are close to or above the Allee threshold. Furthermore, if migration rates are low, one or more than one patch may be successfully invaded, while if migration rates are high all patches are invaded.     

Predator–prey system with strong Allee effect in prey

Global bifurcation analysis of a class of general predator–prey models with a strong Allee effect in prey population is given in details. We show the existence of a point-to-point heteroclinic orbit loop, consider the Hopf bifurcation, and prove the existence/uniqueness and the nonexistence of limit cycle for appropriate range of parameters. For a unique parameter value, a threshold curve separates the overexploitation and coexistence (successful invasion of predator) regions of initial conditions. Our rigorous results justify some recent ecological observations, and practical ecological examples are used to demonstrate our theoretical work.     

Impact of Allee effect on an eco-epidemiological system

In this paper, we propose a general ratio-dependent prey-predator model with disease in predator subject to the strong Allee effect in prey. We obtain the complete dynamics of both models: (a) full model with Allee effect; (b) full model without Allee effect. Model (a) may have more than one interior equilibrium point, but model (b) has only one interior equilibrium point. Numerical results reveal that the coexistence of all the populations at the endemic state is possible for both the models. But for the model with Allee effect, the coexistence can be destroyed by an increased supply of alternative food for the predators. It can also be proved that for the full model with Allee effect, the disease can be suppressed under certain parametric conditions. Also by comparing models (a) and (b), we conclude that Allee effect can create or destroy the interior attractor. Finally, we have studied the disease free-submodel (prey and susceptible predator model) with and without Allee effect. The comparative study between these two submodels leads to the following conclusions: 1) In the presence of Allee effect, the number of interior equilibrium points can change from zero to two whereas the submodel without Allee effect has unique interior equilibrium point; 2) Both with and without Allee effect, initial conditions play an important role on the survival and extinction of prey as well as its corresponding predator; 3) In the presence of Allee effect, bi-stability occurs with stable or periodic coexistence of prey and susceptible predator and the extinction of prey and susceptible predator; 4) Allee effect can generate or destroy the interior equilibrium points.