一个具有年龄结构的单种群离散反应扩散模型的波前解

利用上下解方法研究了一个具有年龄结构的单种群离散反应扩散模型波前解的存在性,并证明了存在具有临界波速的波前解.     

一类具有时空时滞的单种群模型行波解的存在性

通过单调迭代和上下解技术,研究了一类具有时空时滞的单物种种群模型行波解的存在性,证明了当时滞充分小时,方程具有连接两个平衡点的波前解,并得到了一些新的结果.     

一类含时滞的Logistic反应扩散方程的波前解

研究一类含时滞的Logistic滞反应扩散方程的波前解．通过构造合适的上下解,证明了当时滞充分小时,方程存在波前解．用线性化方法,给出了存在波前解的时滞τ取值范围的一个估计．     

一类互惠生态模型解的周期性和爆破

研究了变系数两种群互惠模型解的周期性和爆破性.首先利用上下解和单调迭代方法研究了互惠模型周期解的存在性、稳定性和吸引性,结果表明种群之间的竞争强于互惠时周期解存在.接着利用比较原理得到了解在有限时刻爆破的充分条件,结果表明种群之间的互惠强于之间的竞争时爆破发生.最后通过数值模拟验证了定理的正确性.     

一类格模型行波解的渐近性和唯一性（英文）

研究了一类无穷斑块环境下带年龄结构的单种群格微分时滞生物模型.借助Carr等发展的理论及数学分析的基本技巧和方法,得到了给定系统在s=±∞处波前解的渐近性态和唯一性等性质.     

具年龄结构和时滞的自食种群系统的周期解

利用延拓定理讨论具年龄结构和时滞的自食种群系统正周期解的存在性,得到周期解存在的条件,推广了已有结论.     

一类带参数的泛函微分方程的正周期解的存在性(英文)

利用锥上不动点理论,本文研究了一类非线性泛函微分方程正周期解的存在多样性和ω-周期解的不存在性.获得了一些新的结果.应用这些新的结果,讨论了一类带参数的血细胞生成模型,给出该模型的正周期解的存在性,此结果利用以前的方法是无法得到的.     

一类具扩散和时滞Belousov-Zhabotinskii系统的行波解

研究一般的带时滞的反应扩散方程组的行波解,这儿反应项具混拟单调性质,我们定义了相应的行波解的耦合上下解,以耦合上下解为初始迭代函数构造了耦合迭代序列,并且证明了在一定的单调性条件下该耦合序列收敛于行波解.以一个具体的带时滞的Belousov-Zhabotinskii模型为例,建立了有序的拟上解和拟下解并且得到行波解的存在性.     

捕食者具有阶段结构和基于比率的捕食系统的正周期解

利用重合度理论中的延拓定理,讨论了捕食者具有阶段结构和比率型功能性反应的捕食模型的正周期解的存在性,得到了保证周期解存在的充分条件,推广了已知的相关结果.     

一类具年龄结构和接种的非终生免疫型传染病模型

研究一类具年龄结构和接种的非终生免疫SIRS传染病模型平衡解的稳定性.首先利用特征线法讨论了模型平衡解的存在性,然后利用比较定理和逐次迭代法得到无病平衡解与地方病平衡解全局稳定性的充分条件.     

Neutral Genetic Patterns for Expanding Populations with Nonoverlapping Generations

We investigate the inside dynamics of solutions to integrodifference equations to understand the genetic consequences of a population with nonoverlapping generations undergoing range expansion. To obtain the inside dynamics, we decompose the solution into neutral genetic components. The inside dynamics are given by the spatiotemporal evolution of the neutral genetic components. We consider thin-tailed dispersal kernels and a variety of per capita growth rate functions to classify the traveling wave solutions as either pushed or pulled fronts. We find that pulled fronts are synonymous with the founder effect in population genetics. Adding overcompensation to the dynamics of these fronts has no impact on genetic diversity in the expanding population. However, growth functions with a strong Allee effect cause the traveling wave solution to be a pushed front preserving the genetic variation in the population. In this case, the contribution of each neutral fraction can be computed by a simple formula dependent on the initial distribution of the neutral fractions, the traveling wave solution, and the asymptotic spreading speed.     

Dynamics of prostate cancer stem cells with diffusion and organism response

We develop a systems based model for prostate cancer, as a sub-system of the organism. We accomplish this in two stages. We first start with a general ODE that includes organism response terms. Then, to account for normally observed spatial diffusion of cell populations, the ODE is extended to a PDE that includes spatial terms. Numerical solutions of the full PDE are provided, and are indicative of traveling wave fronts. This motivates the use of a well known transformation to derive a canonically related (non-linear) system of ODEs for traveling wave solutions. For biological feasibility, we show that the non-negative cone for the traveling wave system is time invariant. We also prove that the traveling waves have a unique global attractor. Biologically, the global attractor would be the limit for the avascular tumor growth. We conclude with comments on clinical implications of the model.     

Modeling Spatial Spread of Infectious Diseases with a Fixed Latent Period in a Spatially Continuous Domain

In this paper, with the assumptions that an infectious disease in a population has a fixed latent period and the latent individuals of the population may diffuse, we formulate an SIR model with a simple demographic structure for the population living in a spatially continuous environment. The model is given by a system of reaction-diffusion equations with a discrete delay accounting for the latency and a spatially non-local term caused by the mobility of the individuals during the latent period. We address the existence, uniqueness, and positivity of solution to the initial-value problem for this type of system. Moreover, we investigate the traveling wave fronts of the system and obtain a critical value c ^* which is a lower bound for the wave speed of the traveling wave fronts. Although we can not prove that this value is exactly the minimal wave speed, numeric simulations seem to suggest that it is. Furthermore, the simulations on the PDE model also suggest that the spread speed of the disease indeed coincides with c ^*. We also discuss how the model parameters affect c ^*.     

Sea-urchin feeding fronts

Sea-urchin feeding fronts are a striking example of spatial pattern formation in an ecological system. If it is assumed that urchins are asocial, and that they move randomly, then the formation of these dense fronts is an apparent paradox. The key lies in observations that urchins move further in areas where their algal food is less plentiful. This naturally leads to the accumulation of urchins in areas with abundant algae. If urchin movement is represented as a random walk, with a step size that depends on algal concentration, then their movement may be described by a Fokker–Planck diffusion equation. For certain combinations of algal growth and urchin grazing, traveling wave solutions are obtained. Two-dimensional simulations of urchin algal dynamics show that an initially uniformly distributed urchin population, grazing on an alga with a smoothly varying density, may form a propagating front separating two sharply delineated regions. On one side of the front algal density is uniformly low, and on the other side of the front algal density is uniformly high. Bounds on when stable fronts will form are obtained in terms of urchin density and grazing, and algal growth.     

Global dynamics of a reaction and diffusion model for Lyme disease

This paper is devoted to the mathematical analysis of a reaction and diffusion model for Lyme disease. In the case of a bounded spatial habitat, we obtain the global stability of either disease-free or endemic steady state in terms of the basic reproduction number R?. In the case of an unbounded spatial habitat, we establish the existence of the spreading speed of the disease and its coincidence with the minimal wave speed for traveling fronts. Our analytic results show that R? is a threshold value for the global dynamics and that the spreading speed is linearly determinate.     

Traveling and Pinned Fronts in Bistable Reaction-Diffusion Systems on Networks

Traveling fronts and stationary localized patterns in bistable reaction-diffusion systems have been broadly studied for classical continuous media and regular lattices. Analogs of such non-equilibrium patterns are also possible in networks. Here, we consider traveling and stationary patterns in bistable one-component systems on random Erdös-Rényi, scale-free and hierarchical tree networks. As revealed through numerical simulations, traveling fronts exist in network-organized systems. They represent waves of transition from one stable state into another, spreading over the entire network. The fronts can furthermore be pinned, thus forming stationary structures. While pinning of fronts has previously been considered for chains of diffusively coupled bistable elements, the network architecture brings about significant differences. An important role is played by the degree (the number of connections) of a node. For regular trees with a fixed branching factor, the pinning conditions are analytically determined. For large Erdös-Rényi and scale-free networks, the mean-field theory for stationary patterns is constructed.     

The minimal speed of traveling fronts for a diffusive Lotka-Volterra competition model

This paper concerns the minimal speed of traveling wave fronts for a two-species diffusion-competition model of the Lotka-Volterra type. An earlier paper used this model to discuss the speed of invasion of the gray squirrel by estimating the model parameters from field data, and predicted its speed by the use of a heuristic analytical argument. We discuss the conditions which assure the validity of their argument and show numerically the existence of the realistic range of parameter values for which their heuristic argument does not hold. Especially for the case of the strong interaction of two competing species compared with the intraspecific competition, we show that all parameters appearing in the system affect the minimal speed of invasion. Dedicated to the Memory of Akira Okubo     

Traveling wave solutions in a plant population model with a seed bank

We propose an integro-difference equation model to predict the spatial spread of a plant population with a seed bank. The formulation of the model consists of a nonmonotone convolution integral operator describing the recruitment and seed dispersal and a linear contraction operator addressing the effect of the seed bank. The recursion operator of the model is noncompact, which poses a challenge to establishing the existence of traveling wave solutions. We show that the model has a spreading speed, and prove that the spreading speed can be characterized as the slowest speed of a class of traveling wave solutions by using an asymptotic fixed point theorem. Our numerical simulations show that the seed bank has the stabilizing effect on the spatial patterns of traveling wave solutions.