Effect of hunting cooperation and fear in a predator-prey model

Dynamics of predator-prey systems under the influence of cooperative hunting among predators and the fear thus imposed on the prey population is of great importance from ecological point of view. The role of hunting cooperation and the fear effect in the predator-prey system is gaining considerable attention by the researchers recently. But the study on combined effect of hunting cooperation and fear in the predator-prey system is not yet studied. In the present paper, we investigate the impact of hunting cooperation among predators and predator induced fear in prey population by using the classical predator-prey model. We consider that predator populations cooperate during hunting. We also consider that hunting cooperation induces fear among prey, which has far richer and complex dynamics. We observe that without hunting cooperation, the unique coexistence equilibrium point is globally asymptotically stable. However, an increase in the hunting cooperation induced fear may destabilize the system and produce periodic solution via Hopf-bifurcation. The stability of the Hopf-bifurcating periodic solution is obtained by computing the Lyapunov coefficient. The limit cycles thus obtained may be supercritical or subcritical. We also observe that the system undergoes the Bogdanov-Takens bifurcation in two-parameter space. Further, we observe that the system exhibits backward bifurcation between predator-free equilibrium and coexisting equilibrium. The system also exhibits two different types of bi-stabilities due to subcritical Hopf-bifurcation (between interior equilibrium and stable limit cycle) and backward bifurcation (between predator-free and interior equilibrium points). Further, we observe strong demographic Allee phenomenon in the system. To visualize the dynamical behavior of the system, extensive numerical experiments are performed by using MATLAB and MATCONT softwares.     

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.     

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.     

捕食者具有厌食性反应且食饵具有Allee效应的捕食系统

在Dubis动力系统的基础上,建立了具有Allee效应的捕食系统模型。对系统的稳定性进行了分析,受Allee效应的影响,食饵种群可能因为种群大小处于临界点以下而趋于灭绝。通过对系统进行模拟,结果表明:不受Allee效应的影响,系统的演化属于一种理想化的情形系统到达P(平衡)点的时间较不受Allee效应影响时系统到达P点的时间短,不利于生物的进化,而在Allee效应的影响下,系统的演化将达到一个平衡状态。由此,说明Allee效应为濒临灭绝物种的管理提供了重要的理论依据,对管理部门的决策有参考指导作用。     

Dynamics of stage-structure predator-prey systems under density-dependent effect and mortality

We develop a four dimensional predator-prey system in continuous time with stage-structure for both the communities. The reproduction rate of the prey and the transition rate for the predator, in our model, are assumed to be density-dependent. The stability results for the coexisting equilibrium are obtained by making use of Routh–Hurwitz criteria. Because of the density-dependent effects, numerical simulations are applied in complex situations. We observe that increasing values of the coefficients linked with density-dependent term promote the stability of the coexisting steady state. Our main focus is to understand the variation of stocks when mortality rates on different stage classes are increased. We verified that stable stock on mature predator increases with its increasing mortality rate in three different modeling frameworks. However, no such positive effect on the biomass of the immature predator occurs when immature predators are removed, culled or harvested. Therefore, we could conclude that the appearance of hydra effect on many unstructured predator-prey models is due to the mortality of the mature predator only. No hydra effect is also detected when mature prey is removed in several situations we discussed. Overall, the obtained results are new and could be interesting contribution in theoretical ecology.     

Effect of predator density dependent dispersal of prey on stability of a predator-prey system

This work presents a predator-prey Lotka-Volterra model in a two patch environment. The model is a set of four ordinary differential equations that govern the prey and predator population densities on each patch. Predators disperse with constant migration rates, while prey dispersal is predator density-dependent. When the predator density is large, the dispersal of prey is more likely to occur. We assume that prey and predator dispersal is faster than the local predator-prey interaction on each patch. Thus, we take advantage of two time scales in order to reduce the complete model to a system of two equations governing the total prey and predator densities. The stability analysis of the aggregated model shows that a unique strictly positive equilibrium exists. This equilibrium may be stable or unstable. A Hopf bifurcation may occur, leading the equilibrium to be a centre. If the two patches are similar, the predator density dependent dispersal of prey has a stabilizing effect on the predator-prey system.     

Impacts of Foraging Facilitation Among Predators on Predator-prey Dynamics

Whereas impacts of predator interference on predator-prey dynamics have received considerable attention, the “inverse” process—foraging facilitation among predators—have not been explored yet. Here we show, via mathematical models, that impacts of foraging facilitation on predator-prey dynamics depend on the way this process is modeled. In particular, foraging facilitation destabilizes predator-prey dynamics when it affects the encounter rate between predators and prey. By contrast, it might have a stabilizing effect if the predator handling time of prey is affected. Foraging facilitation is an Allee effect mechanism among predators and we show that for many parameters, it gives rise to a demographic Allee effect or a critical predator density in need to be crossed for predators to persist. We explore also the effects of predator interference, to make the picture “symmetric” and complete. Predator interference is shown to stabilize predator-prey dynamics once its strength is not too high, and thus corroborates results of others. On the other hand, there is a wide range of model parameters for which predator interference gives rise to three co-occurring co-existence equilibria. Such a multi-equilibrial regime is rather robust as we observe it for all the functional response types we explore. This is a previously unreported phenomenon which we show cannot occur for the Beddington–DeAngelis functional response. An interesting topic for future research thus might be to seek for general conditions on predator functional responses that would produce multiple co-existence equilibria in a predator-prey model.     

The impact of mortality on predator population size and stability in systems with stage-structured prey

The relationships between a predator population's mortality rate and its population size and stability are investigated for several simple predator-prey models with stage-structured prey populations. Several alternative models are considered; these differ in their assumptions about the nature of density dependence in the prey's population growth; the nature of stage-transitions; and the stage-selectivity of the predator. Instability occurs at high, rather than low predator mortality rates in most models with highly stage-selective predation; this is the opposite of the effect of mortality on stability in models with homogeneous prey populations. Stage-selective predation also increases the range of parameters that lead to a stable equilibrium. The results suggest that it may be common for a stable predator population to increase in abundance as its own mortality rate increases in stable systems, provided that the predator has a saturating functional response. Sufficiently strong density dependence in the prey generally reverses this outcome, and results in a decrease in predator population size with increasing predator mortality rate. Stability is decreased when the juvenile stage has a fixed duration, but population increases with increasing mortality are still observed in large areas of stable parameter space. This raises two coupled questions which are as yet unanswered; (1) do such increases in population size with higher mortality actually occur in nature; and (2) if not, what prevents them from occurring? Stage-structured prey and stage-related predation can also reverse the 'paradox of enrichment', leading to stability rather than instability when prey growth is increased.     

PREY ADAPTATION AS A CAUSE OF PREDATOR-PREY CYCLES

We analyze simple models of predator-prey systems in which there is adaptive change in a trait of the prey that determines the rate at which it is captured by searching predators. Two models of adaptive change are explored: (1) change within a single reproducing prey population that has genetic variation for vulnerability to capture by the predator; and (2) direct competition between two independently reproducing prey populations that differ in their vulnerability. When an individual predator's consumption increases at a decreasing rate with prey availability, prey adaptation via either of these mechanisms may produce sustained cycles in both species' population densities and in the prey's mean trait value. Sufficiently rapid adaptive change (e.g., behavioral adaptation or evolution of traits with a large additive genetic variance), or sufficiently low predator birth and death rates will produce sustained cycles or chaos, even when the predator-prey dynamics with fixed prey capture rates would have been stable. Adaptive dynamics can also stabilize a system that would exhibit limit cycles if traits were fixed at their equilibrium values. When evolution fails to stabilize inherently unstable population interactions, selection decreases the prey's escape ability, which further destabilizes population dynamics. When the predator has a linear functional response, evolution of prey vulnerability always promotes stability. The relevance of these results to observed predator-prey cycles is discussed.     

食饵庇护所对斑块环境下Leslie-Gower捕食系统的影响

建立了一个显式含有空间庇护所的两斑块Leslie-Gower捕食者-食饵系统。假设只有食饵种群在斑块间以常数迁移率迁移,且在每个斑块上食饵间的迁移比局部捕食者-食饵相互作用发生的时间尺度要快。利用两个时间尺度,可以构建用来描述所有斑块总的食饵和捕食者密度的综合系统。数学分析表明,在一定条件下,存在唯一的正平衡点,并且此平衡点全局稳定。进一步,捕食者的数量随着食饵庇护所数量增加而降低;在一定条件下,食饵的数量随着食饵庇护所数量增加先增加后降低,在足够强的庇护所强度下,两物种出现灭绝。对比以往研究,利用显式含有和隐含空间庇护所的数学模型所得结论不一致,这意味着在研究庇护所对捕食系统种群动态影响时,空间结构可能起着重要作用。     

A comparison of two predator-prey models with Holling's type I functional response

In this paper, we analyze a laissez-faire predator-prey model and a Leslie-type predator-prey model with type I functional responses. We study the stability of the equilibrium where the predator and prey coexist by both performing a linearized stability analysis and by constructing a Lyapunov function. For the Leslie-type model, we use a generalized Jacobian to determine how eigenvalues jump at the corner of the functional response. We show, numerically, that our two models can both possess two limit cycles that surround a stable equilibrium and that these cycles arise through global cyclic-fold bifurcations. The Leslie-type model may also exhibit super-critical and discontinuous Hopf bifurcations. We then present and analyze a new functional response, built around the arctangent, that smoothes the sharp corner in a type I functional response. For this new functional response, both models undergo Hopf, cyclic-fold, and Bautin bifurcations. We use our analyses to characterize predator-prey systems that may exhibit bistability.     

Functional response,numerical response,and stability in arthropod predator-prey ecosystems involving age structure

Summary A general model of arthropod predator-prey systems incorporating age structure in the predator is employed to study the role of functional and numerical responses on stability and the paradox of enrichment. The destabilizing effect of age structure leads to both qualitatively and quantitatively new results for an environment which has an infinite prey carrying capacity, including a lower bound to prey density for a stable equilibrium, a feature not present in models without age structure. When applied to an environment with finite prey carrying capacity, the effect of age structure is to reinforce the arguments implicit to the paradox of enrichment originally developed for traditional models lacking age structure.     

The Lotka-Volterra predator-prey model with foraging-predation risk trade-offs

This article studies the effects of adaptive changes in predator and/or prey activities on the Lotka-Volterra predator-prey population dynamics. The model assumes the classical foraging-predation risk trade-offs: increased activity increases population growth rate, but it also increases mortality rate. The model considers three scenarios: prey only are adaptive, predators only are adaptive, and both species are adaptive. Under all these scenarios, the neutral stability of the classical Lotka-Volterra model is partially lost because the amplitude of maximum oscillation in species numbers is bounded, and the bound is independent of the initial population numbers. Moreover, if both prey and predators behave adaptively, the neutral stability can be completely lost, and a globally stable equilibrium would appear. This is because prey and/or predator switching leads to a piecewise constant prey (predator) isocline with a vertical (horizontal) part that limits the amplitude of oscillations in prey and predator numbers, exactly as suggested by Rosenzweig and MacArthur in their seminal work on graphical stability analysis of predator-prey systems. Prey and predator activities in a long-term run are calculated explicitly. This article shows that predictions based on short-term behavioral experiments may not correspond to long-term predictions when population dynamics are considered.     

Age structure in predator-prey systems. II. Functional response and stability and the paradox of enrichment

We employ the general model of predator-prey systems incorporating age structure in the predator, developed in the previous paper, to study the role of functional response in stability and the paradox of enrichment. The destabilizing effect of age structure leads to both qualitatively and quantitatively new results, including a lower bound to prey density for a stable equilibrium, a feature not present in models without age structure.     

Heteroclinic orbits indicate overexploitation in predator-prey systems with a strong Allee effect

Species establishment in a model system in a homogeneous environment can be dependent not only on the parameter setting, but also on the initial conditions of the system. For instance, predator invasion into an established prey population can fail and lead to system collapse, an event referred to as overexploitation. This phenomenon occurs in models with bistability properties, such as strong Allee effects. The Allee effect then prevents easy re-establishment of the prey species. In this paper, we deal with the bifurcation analyses of two previously published predator-prey models with strong Allee effects. We expand the analyses to include not only local, but also global bifurcations. We show the existence of a point-to-point heteroclinic cycle in these models, and discuss numerical techniques for continuation in parameter space. The continuation of such a cycle in two-parameter space forms the boundary of a region in parameter space where the system collapses after predator invasion, i.e. where overexploitation occurs. We argue that the detection and continuation of global bifurcations in these models are of vital importance for the understanding of the model dynamics.     

Impacts of predation on dynamics of age-structured prey: Allee effects and multi-stability

With a series of mathematical models, we explore impacts of predation on a prey population structured into two age classes, juveniles and adults, assuming generalist, age-specific predators. Predation on any age class is either absent, or represented by types II or III functional responses, in various combinations. We look for Allee effects or more generally for multiple stable steady states in the prey population. One of our key findings is the occurrence of a predator pit (low-density ??refuge?? state of prey induced by predation; the chance of escaping predation thus increases both below and above an intermediate prey density) when only one age class is consumed and predators use a type II functional response ??this scenario is known to occur for an unstructured prey consumed via a type III functional response and can never occur for an unstructured prey consumed via a type II one. In the case where both age classes are consumed by type II generalist predators, an Allee effect occurs frequently, but some parameters give also rise to a predator pit and even three stable equilibria (one extinction equilibrium and two positive ones??Allee effect and predator pit combined). Multiple positive stable equilibria are common if one age class is consumed via a type II functional response and the other via a type III functional response??here, in addition to the behaviours mentioned above one may even observe three stable positive equilibria????double?? predator pit. Some of these results are discussed from the perspective of population management.     

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.     

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.     

Influence of density dependence on predator-prey seabird interactions at large spatio-temporal scales

Theoretical investigations of competitive dynamics have noted that numbers of predator and prey influence each other. However, few empirical studies have demonstrated how a life-history trait of the prey (such as fecundity) can be affected simultaneously by its own density and the density of predators. For instance, density dependence can reduce fecundity with increasing number of prey, while inverse density dependence or Allee effects may occur especially when the prey is a social organism. Here we analysed an intraguild predator-prey system of two seabird species at a large spatio-temporal scale. As expected, we found that fecundity of prey was negatively affected by predator density. Nevertheless, fecundity of prey also increased nonlinearly with its own density and strikingly with the prey-predator ratio. Small groups of prey were probably not able to defend their nests especially against large number of predators. At the highest prey densities (i.e. when anti-predator strategies should be most efficient), prey fecundity also lowered, suggesting the appearance of density dependence mediated by food competition. Allee effects and density dependence occurred across a broad range of population sizes of both the prey and the predator at several local populations facing different ecological environments.     

Bubbling and hydra effect in a population system with Allee effect

We present a continuous time predator-prey model and predator’s growth subjected to component Allee effect. The model also includes density dependent mortality of predator. We investigate our model both analytically and numerically, and highlighted the effect of density independent mortality and Allee effect. In our system, we find that a fixed point representing the extinction of predator is always a stable point. When coexistence equilibria exists our system is bistable. We have observed that tristability is possible for our model that includes two stable co-existence fixed point. The most important phenomena which we have observed are hydra effect and cascading effect. Due to component Allee effect in predator the system shows multiple hydra effect. We discuss the phenomenon of bubbling, which indicates increasing and decreasing of amplitudes of cycles. We have presented one-parametric as well as two-parametric bifurcation diagram and also all possible bifurcations that the system could go through.