Competition between plasmid-bearing and plasmid-free organisms in a chemostat with pulsed input and washout.
Intra-specific competition in population dynamics can be described by integro-differential equations where the integral term corresponds to nonlocal consumption of resources by individuals of the same population. Already the single integro-differential equation can show the emergence of nonhomogeneous in space stationary structures and can be used to model the process of speciation, in particular, the emergence of biological species during evolution [S. Genieys et al., Math. Model. Nat. Phenom....
We develop a stage-structured model that describes the dynamics of two competing species each of which have sexual and clonal reproduction. This is typical of many plants including irises. We first analyze the dynamical behavior of a single species model. We show that when the inherent net reproductive number is smaller than one then the population will go to extinction and if it is larger than one then an interior equilibrium exists and it is globally asymptotically stable. Then we analyze...
We introduce and study conditional differential equations, a kind of random differential equations. We give necessary and sufficient conditions for the existence of a solution of such an equation. We apply our main result to a Malthus type model.
This paper provides an introduction to delay differential equations together with a short survey on state-dependent delay differential equations arising in population dynamics. Our main goal is to examine how the delays emerge from inner mechanisms in the model, how they induce oscillations and stability switches in the system and how the qualitative behaviour of a biological model depends on the form of the delay.
An eco-epidemiological model of susceptible Tilapia fish, infected Tilapia fish and Pelicans is investigated by several author based upon the work initiated by Chattopadhyay and Bairagi (Ecol. Model., 136, 103–112, 2001). In this paper, we investigate the dynamics of the same model by considering different parameters involved with the model as bifurcation parameters in details. Considering the intrinsic growth rate of susceptible Tilapia fish as bifurcation parameter, we demonstrate the period doubling...
Two models of microbial growth are derived as a resuslt of a discussion of the models of Monod and Hinshelwood types. The approach takes account of the lyse of dead cells in inhibitory products as well as in those which stimulate the growth. The asymptotic behaviour of the models is proved and the models applied to a chemostat.
In this paper we present an epidemic model affecting an age-structured population. We show by numerical simulations that this demographic structure can induce persistent oscillations in the epidemic. The model is then extended to encompass a stage-structured disease within an age-dependent population. In this case as well, persistent oscillations are observed in the infected as well as in the whole population.
Computer simulation of a few thousands of particles moving (approximately) according to the energy and momentum conservation laws on a tessellation of squares in discrete time steps and interacting according to the predator-prey scheme is analyzed. The population dynamics are described by the basic Lotka-Volterra interactions (multiplication of preys, predation and multiplication of predators, death of predators), but the spatial effects result in differences between the system evolution and the...
A Volterra model with mutual interference concerning integrated pest management is proposed and analyzed. By using Floquet theorem and small amplitude perturbation method and comparison theorem, we show the existence of a globally asymptotically stable pest-eradication periodic solution. Further, we prove that when the stability of pest-eradication periodic solution is lost, the system is permanent and there exists a locally stable positive periodic solution which arises from the pest-eradication...