Abstract

Reaction-telegraph equation (RTE) is a mathematical model that has often been used to describe natural phenomena, with specific applications ranging from physics to social sciences. In particular, in the context of ecology, it is believed to be a more realistic model to describe animal movement than the more traditional approach based on the reaction-diffusion equations. Indeed, the reaction-telegraph equation arises from more realistic microscopic assumptions about individual animal movement (the correlated random walk) and hence could be expected to be more relevant than the diffusion-type models that assume the simple, unbiased Brownian motion. However, the RTE has one significant drawback as its solutions are not positively defined. It is not clear at which stage of the RTE derivation the realism of the microscopic description is lost and/or whether the RTE can somehow be ‘improved’ to guarantee the solutions positivity. Here we show that the origin of the problem is twofold. Firstly, the RTE is not fully equivalent to the Cattaneo system from which it is obtained; the equivalence can only be achieved in a certain parameter range and only for the initial conditions containing a finite number of Fourier modes. Secondly, the Dirichlet type boundary conditions routinely used for reaction-diffusion equations appear to be meaningless if used for the RTE resulting in solutions with unrealistic properties. We conclude that, for the positivity to be regained, one has to use the Cattaneo system with boundary conditions of Robin type or Neumann type, and we show how relevant classes of solutions can be obtained.

Highlights

  • Mathematical modelling is a powerful and widely used toolbox of theoretical ecology [1, 2, 3, 4, 5]

  • If we look at equation (8b), a no-flux condition implies that the spatial derivative of the density at the boundaries should be zero, which is just a Neumann boundary condition if we consider the reaction-telegraph equation (9)

  • The reaction-telegraph equation is obtained by some apparently identical mathematical transformations from the reaction-Cattaneo system where the latter arise as a result of counting animals moving in different directions and is positively defined by definition

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Summary

Introduction

Mathematical modelling is a powerful and widely used toolbox of theoretical ecology [1, 2, 3, 4, 5]. Regarded as a more adequate model than the reaction-diffusion equation and it was used successfully in several studies to understand the dynamics of real world populations and/or to sensibly interpret field data [30, 43, 44, 45] As it happens, the RTE has some unrealistic properties too, as its solutions are not positively defined, i.e. can become negative at some locations in space and/or at some moments of time [29, 46, 47]. In any derivation of the telegraph or reaction-telegraph equation, the next-to-final stage is given by the Cattaneo system which is essentially a system of mass-balance equations In case this system is considered in an unbounded space, its solutions are positively defined [30]. Note that the dimensionless form (9) of the RTE cannot be obtained from the telegraph equation (6) just by adding the growth term to the right-hand side (as is done in case of diffusion) as it would miss the new factor (1 − μ) in the left-hand side, cf. [30]

Dirichlet boundary conditions
Consistency of the solution with the Cattaneo system
General solution for the Cattaneo system
Robin boundary conditions
Sufficient condition of the solution positivity
Zero flux boundary condition
Discussion and conclusions
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