Abstract: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 patc… Show more
“…This bound is similar to, but tighter than, previously deduced bounds that ensure the prey-only system is stationary (Keitt et al, 2000). Figure 15 shows the above analytical bound, regions for invading and stationary solutions for the prey-only model (35) with v ≡ 0, and regions for invading, stationary and receding solutions for the full predator-prey system (35).…”
Section: Noninvasive Solutionssupporting
confidence: 77%
“…16 below). A similar phenomenon has been analysed by Keitt et al (2000) in an ecological context for the prey-only model. It also arises as so-called 'propagation failure' in models for excitable systems in physiology (Keener, 1987(Keener, , 1993.…”
Observations on Mount St Helens indicate that the spread of recolonizing lupin plants has been slowed due to the presence of insect herbivores and it is possible that the spread of lupins could be reversed in the future by intense insect herbivory [Fagan, W. F. and J. Bishop (2000). Trophic interactions during primary sucession: herbivores slow a plant reinvasion at Mount St. Helens. Amer. Nat. 155, [238][239][240][241][242][243][244][245][246][247][248][249][250][251]. In this paper we investigate mechanisms by which herbivory can contain the spatial spread of recolonizing plants. Our approach is to analyse a series of predatorprey reaction-diffusion models and spatially coupled ordinary differential equation models to derive conditions under which predation pressure can slow, stall or reverse a spatial invasion of prey. We focus on models where prey disperse more slowly than predators. We comment on the types of functional response which give such solutions, and the circumstances under which the models are appropriate.
“…This bound is similar to, but tighter than, previously deduced bounds that ensure the prey-only system is stationary (Keitt et al, 2000). Figure 15 shows the above analytical bound, regions for invading and stationary solutions for the prey-only model (35) with v ≡ 0, and regions for invading, stationary and receding solutions for the full predator-prey system (35).…”
Section: Noninvasive Solutionssupporting
confidence: 77%
“…16 below). A similar phenomenon has been analysed by Keitt et al (2000) in an ecological context for the prey-only model. It also arises as so-called 'propagation failure' in models for excitable systems in physiology (Keener, 1987(Keener, , 1993.…”
Observations on Mount St Helens indicate that the spread of recolonizing lupin plants has been slowed due to the presence of insect herbivores and it is possible that the spread of lupins could be reversed in the future by intense insect herbivory [Fagan, W. F. and J. Bishop (2000). Trophic interactions during primary sucession: herbivores slow a plant reinvasion at Mount St. Helens. Amer. Nat. 155, [238][239][240][241][242][243][244][245][246][247][248][249][250][251]. In this paper we investigate mechanisms by which herbivory can contain the spatial spread of recolonizing plants. Our approach is to analyse a series of predatorprey reaction-diffusion models and spatially coupled ordinary differential equation models to derive conditions under which predation pressure can slow, stall or reverse a spatial invasion of prey. We focus on models where prey disperse more slowly than predators. We comment on the types of functional response which give such solutions, and the circumstances under which the models are appropriate.
“…because mating encounters are rare) [34]. Apparent competition: indirect interaction leading to negative effects of one species on another, mediated through a shared natural enemy, such as predators and parasites.…”
“…We start analysis of the model (10) by observing that, provided (w in − w out ) is sufficiently small and the initial lake population is also small, then the invader population in the lake will remain small (see also [13]). Proposition 1.…”
Section: Critical Flowmentioning
confidence: 99%
“…The importance of Allee effect for spatio-temporal dynamics of biological invasions has been shown in [16,13,8]. It appears that in presence of the effect the invasion front can move slower, stop, or even reverse its direction.…”
Abstract. 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.
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