Epidemic Models as Scaling Limits of Individual Dynamics

Infection spread among individuals is modelled with a continuous time Markov chain, in which subject interactions depend on their distance in space. The well known SIR model and non local variants of the latter are then obtained as large scale limits of the individual based model in two different scaling regimes of the interaction.Comment: 22 page

Existence and asymptotics of traveling wave fronts for a coupled nonlocal diffusion and difference system with delay

In this paper, we consider a general study of a recent proposed hematopoietic stem cells model. This model is a combination of nonlocal diffusion equation and difference equation with delay. We deal with the properties of traveling waves for this system such as the existence and asymptotic behavior. By using the Schauder’s fixed point theorem combined with the method based on the construction of upper and lower solutions, we obtain the existence of traveling wave fronts for a speed c > c . The case c = c is studied by using a limit argument. We prove also that c is the critical value. We finally prove that the nonlocality increases the minimal wave speed

Fractional derivative models for the spread of diseases

This thesis considers the mathematical modelling of disease, using fractional differential equations in order to provide a tool for the description of memory effects. In Chapter 3 we illustrate a commensurate fractional order tumor model, and we find a critical value of the fractional derivative dependent on the parameter values of the model. For fractional derivatives of orders less than the critical value an unstable equilibrium point of the system becomes stable. In order to show changes in the observed areas of attraction of two stable points in the system, we then consider a fractional order SIR epidemic model and investigate the change from a monostable to a bistable system.;Chapter 4 considers a model for virus dynamics where the fractional orders for populations are different, called an incommensurate system. An approximate analytical solution for the characteristic equation of the incommensurate model is found when the different fractional orders are similar and close to the critical value of the fractional order of the commensurate system. In addition, the instability boundary is found as a function of both parameters. A comparison between analytical and numerical results shows the high accuracy of this approximation.;Chapter 5 consists of two parts, in the first part we generalise the integer Fisher's equation to be a space-time fractional differential equation and consider travelling wave solutions. In the second part we generalise an integer SIR model with spatial heterogeneity, which was studied by Murray [117], to a space-time fractional derivative model. We apply the (G0/G)-expansion method and find travelling wave solutions, although in this case we must consider the Jumarie's modified Riemann-Liouville fractional derivative. Finally, we consider the effect of changing the orders of time and space fractional derivatives on the location and speed of the travelling wave solution.This thesis considers the mathematical modelling of disease, using fractional differential equations in order to provide a tool for the description of memory effects. In Chapter 3 we illustrate a commensurate fractional order tumor model, and we find a critical value of the fractional derivative dependent on the parameter values of the model. For fractional derivatives of orders less than the critical value an unstable equilibrium point of the system becomes stable. In order to show changes in the observed areas of attraction of two stable points in the system, we then consider a fractional order SIR epidemic model and investigate the change from a monostable to a bistable system.;Chapter 4 considers a model for virus dynamics where the fractional orders for populations are different, called an incommensurate system. An approximate analytical solution for the characteristic equation of the incommensurate model is found when the different fractional orders are similar and close to the critical value of the fractional order of the commensurate system. In addition, the instability boundary is found as a function of both parameters. A comparison between analytical and numerical results shows the high accuracy of this approximation.;Chapter 5 consists of two parts, in the first part we generalise the integer Fisher's equation to be a space-time fractional differential equation and consider travelling wave solutions. In the second part we generalise an integer SIR model with spatial heterogeneity, which was studied by Murray [117], to a space-time fractional derivative model. We apply the (G0/G)-expansion method and find travelling wave solutions, although in this case we must consider the Jumarie's modified Riemann-Liouville fractional derivative. Finally, we consider the effect of changing the orders of time and space fractional derivatives on the location and speed of the travelling wave solution

The spatio-temporal dynamics of neutral genetic diversity

International audienceThe notions of pulled and pushed solutions of reaction-dispersal equations introduced by Garnier et al. (2012) and Roques et al. (2012) are based on a decomposition of the solutions into several components. In the framework of population dynamics, this decomposition is related to the spatio-temporal evolution of the genetic structure of a population. The pulled solutions describe a rapid erosion of neutral genetic diversity, while the pushed solutions are associated with a maintenance of diversity. This paper is a survey of the most recent applications of these notions to several standard models of population dynamics, including reaction-diffusion equations and systems and integro-differential equations. We describe several counterintuitive results, where unfavorable factors for the persistence and spreading of a population tend to promote diversity in this population. In particular, we show that the Allee effect, the existence of a competitor species, as well as the presence of climate constraints are factors which can promote diversity during a colonization. We also show that long distance dispersal events lead to a higher diversity, whereas the existence of a nonreproductive juvenile stage does not affect the neutral diversity in a range-expanding population