On multidimensional discrete-time Beverton–Holt competition models

Following Ackleh et al. (2005), we study the multidimensional discrete-time competitive Beverton–Holt equations with equal interspecific competition coefficients. It is shown that competitive exclusion occurs if only one species has the largest carrying capacity. Otherwise, all the species with the largest carrying capacity coexist. In the former case, the system is globally asymptotically stable. In the latter case, the system has a linear stable manifold.     

The Beverton–Holt dynamic equation

The Cushing–Henson conjectures on time scales are presented and verified. The central part of these conjectures asserts that based on a model using the dynamic Beverton–Holt equation, a periodic environment is deleterious for the population. The proof technique is as follows. First, the Beverton–Holt equation is identified as a logistic dynamic equation. The usual substitution transforms this equation into a linear equation. Then the proof is completed using a recently established dynamic version of the generalized Jensen inequality.     

A stochastic modified Beverton–Holt model with the Allee effect

In this paper, we consider a discrete stochastic Beverton–Holt model with the Allee effect. We study the effects of demographic and environmental fluctuations on the dynamics of the model. Moreover, we investigate the potential function, the attainment time and quasi-stationary distributions of the system.     

Ornstein–Uhlenbeck operators with time periodic coefficients

We study the realization of the differential operator in the space of continuous time periodic functions, and in L ² with respect to its (unique) invariant measure. Here L(t) is an Ornstein-Uhlenbeck operator in , such that L(t + T) = L(t) for each .      

A nonautonomous Beverton–Holt equation of higher order

In this paper, we discuss a certain nonautonomous Beverton–Holt equation of higher order. After a brief introduction to the classical Beverton–Holt equation and recent results, we solve the higher-order Beverton–Holt equation by rewriting the recurrence relation as a difference system of order one. In this process, we examine the existence and uniqueness of a periodic solution and its global attractivity. We continue our analysis by studying the corresponding second Cushing–Henson conjecture, i.e., by relating the average of the unique periodic solution to the average of the carrying capacity.     

Almost automorphic solutions to a Beverton–Holt dynamic equation with survival rate

In this paper we study and obtain the existence of an almost automorphic solution to a Beverton–Holt dynamic equation with a nonconstant survival rate under some reasonable assumptions.     

Optimal impulsive harvesting on non-autonomous Beverton–Holt difference equations

Many recent advances in the theory of the optimal economic exploitation of renewable fish resources have been gained by applying optimal control theory. However, despite these successes, much less is known about how seasonal environments affect the maximum sustainable yield (MSY) (or population persistence) and any effects of relations between intensity and frequency of harvesting. Assuming that fish populations follow Beverton–Holt equations we investigated impulsive harvesting in seasonal environments, focusing on both economic aspects and resource sustainability. We first investigated the existence and stability of a periodic solution and its analytic formula, and then showed that the population persistence depends on the intensity and frequency of harvesting. With the MSY as a management objective, we investigated optimal impulsive harvesting policies. The optimal harvesting effort that maximizes the sustainable yield, the corresponding optimal population level, and the MSY are obtained by using discrete Euler–Lagrange equations and product formulae, and their explicit expressions were obtained in terms of the intrinsic growth rate, the carrying capacity, and the impulsive moments. These results imply that harvest timing is of crucial importance to the MSY. Since impulsive differential equations incorporate elements of continuous and discrete systems, we can apply all results obtained for Beverton–Holt equations with impulsive effects to periodic logistic equations with impulsive harvesting.     

Stochastic modified Beverton–Holt model with Allee effect II: the Cushing–Henson conjecture

We consider a single-species stochastic modified Beverton–Holt model with Allee effects caused by predator saturation. We prove that, under some conditions on the parameters, there exists a Markov operator that is asymptotically stable. A stochastic version of the Cushing–Henson conjecture on attenuance and resonance is investigated.     

Periodic solutions of “predator–prey” systems with continuous delay and periodic coefficients

We prove the existence of positive ω-periodic solutions for some “predator–prey” systems with continuous delay of the argument for the case where the parameters of these systems are specified by ω-periodic continuous positive functions.     

Stochastic Burgers PDEs with random coefficients and a generalization of the Cole–Hopf transformation

This paper studies forward and backward versions of the random Burgers equation (RBE) with stochastic coefficients. First, the celebrated Cole–Hopf transformation reduces the forward RBE to a forward random heat equation (RHE) that can be treated pathwise. Next we provide a connection between the backward Burgers equation and a system of FBSDEs. Exploiting this connection, we derive a generalization of the Cole–Hopf transformation which links the backward RBE with the backward RHE and investigate the range of its applicability. Stochastic Feynman–Kac representations for the solutions are provided. Explicit solutions are constructed and applications in stochastic control and mathematical finance are discussed.     

Diffusive Holling–Tanner predator–prey models in periodic environments

In this paper, by using the Lyapunov method, we establish sufficient conditions for the global asymptotic stability of the positive periodic solution to diffusive Holling–Tanner predator–prey models with periodic coefficients and no-flux conditions.     

Discrete-time models for releases of sterile mosquitoes with Beverton–Holt-type of survivability

In this paper, we formulate discrete-time mathematical models for the interactive wild and sterile mosquitoes. Instead of the Ricker-type of nonlinearity for the survival functions, we assume the Beverton–Holt-type in these models. We consider three different strategies for the releases of sterile mosquitoes and investigate the model dynamics. Threshold values for the releases of sterile mosquitoes are derived for all of the models that determine whether the wild mosquitoes are wiped out or coexist with the sterile mosquitoes. Numerical examples are given to demonstrate the dynamics of the models.     

Time-consistent investment-proportional reinsurance strategy with random coefficients for mean–variance insurers

In this study, we consider an insurer who manages her underlying risk by purchasing proportional reinsurance and investing in a financial market consisting of a risk-free bond and a risky asset. The objective of the insurer is to identify an investment–reinsurance strategy that minimizes the mean–variance cost function. We obtain a time-consistent open-loop equilibrium strategy and the corresponding efficient frontier in explicit form using two systems of backward stochastic differential equations. Furthermore, we apply our results to Vasiček’s stochastic interest rate model and Heston’s stochastic volatility model. In both cases, we obtain a closed-form solution.     

Dynamical behaviors of fuzzy reaction–diffusion periodic cellular neural networks with variable coefficients and delays

When modeling neural networks in a real world, not only diffusion effect and fuzziness cannot be avoided, but also self-inhibitions, interconnection weights, and inputs should vary as time varies. In this paper, we discuss the dynamical behaviors of delayed reaction–diffusion fuzzy cellular neural networks with varying periodic self-inhibitions, interconnection weights as well as inputs. By using Halanay’s delay differential inequality, M$M$-matrix theory and analytic methods, some new sufficient conditions are obtained to ensure the existence, uniqueness, and global exponential stability of the periodic solution, and the exponentially convergent rate index is also estimated. In particular, the traditional assumption on the differentiability of the time-varying delays is no longer needed. The methodology developed in this paper is shown to be simple and effective for the exponential periodicity and stability analysis of neural networks with time-varying delays. Two examples are given to show the usefulness of the obtained results that are less restrictive than recently known criteria.     

Spectrum and pseudospectrum of non-self-adjoint Schrödinger operators with periodic coefficients

We consider the pseudospectrum of the non-self-adjoint operator $$\mathfrak{D} = - h^2 \frac{{d^2 }}{{dx^2 }} + iV(x)$$ , where V(x) is a periodic entire analytic function, real on the real axis, with a real period T. In this operator, h is treated as a small parameter. We show that the pseudospectrum of this operator is the closure of its numerical image, i.e., a half-strip in ?. In this case, the pseudoeigenfunctions, i.e., the functions ?(h, x) satisfying the condition $$\left\| {\mathfrak{D}\varphi - \lambda \varphi } \right\| = O(h^N ), \left\| \varphi \right\| = 1, N \in \mathbb{N}$$ , can be constructed explicitly. Thus, it turns out that the pseudospectrum of the operator under study is much wider than its spectrum.     

Dynamics of a generalized Ricker–Beverton–Holt competition model subject to Allee effects

In this article, we propose and study a generalized Ricker–Beverton–Holt competition model subject to Allee effects to obtain insights on how the interplay of Allee effects and contest competition affects the persistence and the extinction of two competing species. By using the theory of monotone dynamics and the properties of critical curves for non-invertible maps, our analysis show that our model has relatively simple dynamics, i.e. almost every trajectory converges to a locally asymptotically stable equilibrium if the intensity of intra-specific competition intensity exceeds that of inter-specific competition. This equilibrium dynamics is also possible when the intensity of intra-specific competition intensity is less than that of inter-specific competition but under conditions that the maximum intrinsic growth rate of one species is not too large. The coexistence of two competing species occurs only if the system has four interior equilibria. We provide an approximation to the basins of the boundary attractors (i.e. the extinction of one or both species) where our results suggests that contest species are more prone to extinction than scramble ones are at low densities. In addition, in comparison to the dynamics of two species scramble competition models subject to Allee effects, our study suggests that (i) Both contest and scramble competition models can have only three boundary attractors without the coexistence equilibria, or four attractors among which only one is the persistent attractor, whereas scramble competition models may have the extinction of both species as its only attractor under certain conditions, i.e. the essential extinction of two species due to strong Allee effects; (ii) Scramble competition models like Ricker type models can have much more complicated dynamical structure of interior attractors than contest ones like Beverton–Holt type models have; and (iii) Scramble competition models like Ricker type competition models may be more likely to promote the coexistence of two species at low and high densities under certain conditions: At low densities, weak Allee effects decrease the fitness of resident species so that the other species is able to invade at its low densities; While at high densities, scramble competition can bring the current high population density to a lower population density but is above the Allee threshold in the next season, which may rescue a species that has essential extinction caused by strong Allee effects. Our results may have potential to be useful for conservation biology: For example, if one endangered species is facing essential extinction due to strong Allee effects, then we may rescue this species by bringing another competing species subject to scramble competition and Allee effects under certain conditions.