572 research outputs found

    Spatiotemporal dynamics in a spatial plankton system

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    In this paper, we investigate the complex dynamics of a spatial plankton-fish system with Holling type III functional responses. We have carried out the analytical study for both one and two dimensional system in details and found out a condition for diffusive instability of a locally stable equilibrium. Furthermore, we present a theoretical analysis of processes of pattern formation that involves organism distribution and their interaction of spatially distributed population with local diffusion. The results of numerical simulations reveal that, on increasing the value of the fish predation rates, the sequences spots →\rightarrow spot-stripe mixtures→\rightarrow stripes→\rightarrow hole-stripe mixtures holes→\rightarrow wave pattern is observed. Our study shows that the spatially extended model system has not only more complex dynamic patterns in the space, but also has spiral waves.Comment: Published Pape

    Revisiting the stability of spatially heterogeneous predator-prey systems under eutrophication

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    We employ partial integro-differential equations to model trophic interaction in a spatially extended heterogeneous environment. Compared to classical reaction-diffusion models, this framework allows us to more realistically describe the situation where movement of individuals occurs on a faster time scale than the demographic (population) time scale, and we cannot determine population growth based on local density. However, most of the results reported so far for such systems have only been verified numerically and for a particular choice of model functions, which obviously casts doubts about these findings. In this paper, we analyse a class of integro-differential predator-prey models with a highly mobile predator in a heterogeneous environment, and we reveal the main factors stabilizing such systems. In particular, we explore an ecologically relevant case of interactions in a highly eutrophic environment, where the prey carrying capacity can be formally set to 'infinity'. We investigate two main scenarios: (i) the spatial gradient of the growth rate is due to abiotic factors only, and (ii) the local growth rate depends on the global density distribution across the environment (e.g. due to non-local self-shading). For an arbitrary spatial gradient of the prey growth rate, we analytically investigate the possibility of the predator-prey equilibrium in such systems and we explore the conditions of stability of this equilibrium. In particular, we demonstrate that for a Holling type I (linear) functional response, the predator can stabilize the system at low prey density even for an 'unlimited' carrying capacity. We conclude that the interplay between spatial heterogeneity in the prey growth and fast displacement of the predator across the habitat works as an efficient stabilizing mechanism.Comment: 2 figures; appendices available on request. To appear in the Bulletin of Mathematical Biolog

    A Holling-Tanner predator-prey model with strong Allee effect

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    We analyse a modified Holling-Tanner predator-prey model where the predation functional response is of Holling type II and we incorporate a strong Allee effect associated with the prey species production. The analysis complements results of previous articles by Saez and Gonzalez-Olivares (SIAM J. Appl. Math. 59 1867-1878, 1999) and Arancibia-Ibarra and Gonzalez-Olivares (Proc. CMMSE 2015 130-141, 2015)discussing Holling-Tanner models which incorporate a weak Allee effect. The extended model exhibits rich dynamics and we prove the existence of separatrices in the phase plane separating basins of attraction related to co-existence and extinction of the species. We also show the existence of a homoclinic curve that degenerates to form a limit cycle and discuss numerous potential bifurcations such as saddle-node, Hopf, and Bogadonov-Takens bifurcations

    Spatiotemporal pattern induced by self and cross-diffusion in a spatial Holling-Tanner model

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    In this paper, we have made an attempt to provide a unified framework to understand the complex spatiotemporal patterns induced by self and cross diffusion in a spatial Holling-Tanner model forphytoplankton-zooplankton-fish interaction. The effect of critical wave length which can drive the system to instability is investigated. We have examined the criterion between two cross-diffusivity (constant and timevarying)on the stability of the model system and for diffusive instability to occur. Based on these conditions and by performing a series of extensive simulations, we observed the irregular patterns, stationary strips, spots, and strips-spots mixture patterns. Numerical simulation results reveal that the regular strip-spot mixture patterns prevail over the whole domain on increasing the values of self- diffusion coefficients of phytoplankton and zooplankton and the dynamics of the system do not undergo any further changes

    Bistability induced by generalist natural enemies can reverse pest invasions

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    Reaction-diffusion analytical modeling of predator-prey systems has shown that specialist natural enemies can slow, stop and even reverse pest invasions, assuming that the prey population displays a strong Allee effect in its growth. Few additional analytical results have been obtained for other spatially distributed predator-prey systems, as traveling waves of non-monotonous systems are notoriously difficult to obtain. Traveling waves have indeed recently been shown to exist in predator-prey systems, but the direction of the wave, an essential item of information in the context of the control of biological invasions, is generally unknown. Preliminary numerical explorations have hinted that control by generalist predators might be possible for prey populations displaying logistic growth. We aimed to formalize the conditions in which spatial biological control can be achieved by generalists, through an analytical approach based on reaction-diffusion equations. The population of the focal prey - the invader - is assumed to grow according to a logistic function. The predator has a type II functional response and is present everywhere in the domain, at its carrying capacity, on alternative hosts. Control, defined as the invader becoming extinct in the domain, may result from spatially independent demographic dynamics or from a spatial extinction wave. Using comparison principles, we obtain sufficient conditions for control and for invasion, based on scalar bistable partial differential equations (PDEs). The searching efficiency and functional response plateau of the predator are identified as the main parameters defining the parameter space for prey extinction and invasion. Numerical explorations are carried out in the region of those control parameters space between the super-and subso-lutions, in which no conclusion about controllability can be drawn on the basis of analytical solutions. The ability of generalist predators to control prey populations with logistic growth lies in the bis-table dynamics of the coupled system, rather than in the bistability of prey-only dynamics as observed for specialist predators attacking prey populations displaying Allee effects. The consideration of space in predator-prey systems involving generalist predators with a parabolic functional response is crucial. Analysis of the ordinary differential equations (ODEs) system identifies parameter regions with monostable (extinction) and bistable (extinction or invasion) dynamics. By contrast, analysis of the associated PDE system distinguishes different and additional regions of invasion and extinction. Depending on the relative positions of these different zones, four patterns of spatial dynamics can be identified : traveling waves of extinction and invasion, pulse waves of extinction and heterogeneous stationary positive solutions of the Turing type. As a consequence, prey control is predicted to be possible when space is considered in additional situations other than those identified without considering space. The reverse situation is also possible. None of these considerations apply to spatial predator-prey systems with specialist natural enemies
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