We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
Coffee berry diseases (CBD) pose significant threats to coffee production worldwide, affecting the livelihoods of millions of farmers and the global coffee market. Fractional calculus provides a powerful framework for describing non-local and memory-dependent phenomena, making it suitable for modelling the long-range interactions inherent in CBD spread. This study aims to formulate and analyse fractional order model for CBD transmission dynamics in the sense of Atangana–Baleanu–Caputo. Fixed point theorems were utilised to test the existence and uniqueness of the model’s solutions using fractional order. The basic reproduction number was calculated utilising the next-generation matrix. The model has locally asymptotically stable equilibrium positions (disease-free and endemic). Furthermore, the Lyapunov function was used to conduct a global stability analysis of the equilibrium locations. A numerical simulation of the CBD model was created using the fractional Adam–Bashforth–Moulton approach to validate the analytical findings. Our findings contribute to the development of more accurate predictive models and inform the design of targeted interventions to mitigate the impact of CBD on coffee production systems.
In this paper, we study the existence of travelling wave solutions and the spreading speed for the solutions of an age-structured epidemic model with nonlocal diffusion. Our proofs make use of the comparison principles both to construct suitable sub/super-solutions and to prove the regularity of travelling wave solutions.
We introduce a free boundary model to study the effect of vesicle transport onto neurite growth. It consists of systems of drift-diffusion equations describing the evolution of the density of antero- and retrograde vesicles in each neurite coupled to reservoirs located at the soma and the growth cones of the neurites, respectively. The model allows for a change of neurite length as a function of the vesicle concentration in the growth cones. After establishing existence and uniqueness for the time-dependent problem, we briefly comment on possible types of stationary solutions. Finally, we provide numerical studies on biologically relevant scales using a finite volume scheme. We illustrate the capability of the model to reproduce cycles of extension and retraction.
We study the Cauchy problem on the real line for the nonlocal Fisher-KPP equation in one spatial dimension,
\begin{equation*} u_t = D u_{xx} + u(1-\phi *u), \end{equation*}
where $\phi *u$ is a spatial convolution with the top hat kernel, $\phi (y) \equiv H\left (\frac{1}{4}-y^2\right )$. After observing that the problem is globally well-posed, we demonstrate that positive, spatially periodic solutions bifurcate from the spatially uniform steady state solution $u=1$ as the diffusivity, $D$, decreases through $\Delta _1 \approx 0.00297$ (the exact value is determined in Section 3). We explicitly construct these spatially periodic solutions as uniformly valid asymptotic approximations for $D \ll 1$, over one wavelength, via the method of matched asymptotic expansions. These consist, at leading order, of regularly spaced, compactly supported regions with width of $O(1)$ where $u=O(1)$, separated by regions where $u$ is exponentially small at leading order as $D \to 0^+$. From numerical solutions, we find that for $D \geq \Delta _1$, permanent form travelling waves, with minimum wavespeed, $2 \sqrt{D}$, are generated, whilst for $0 \lt D \lt \Delta _1$, the wavefronts generated separate the regions where $u=0$ from a region where a steady periodic solution is created via a distinct periodic shedding mechanism acting immediately to the rear of the advancing front, with this mechanism becoming more pronounced with decreasing $D$. The structure of these transitional travelling wave forms is examined in some detail.
We provide well-posedness results for nonlinear parabolic partial differential equations (PDEs) given by reaction–diffusion equations describing the concentration of oxygen in encapsulated cells. The cells are described in terms of a core and a shell, which introduces a discontinuous diffusion coefficient as the material properties of the core and shell differ. In addition, the cells are subject to general nonlinear consumption of oxygen. As no monotonicity condition is imposed on the consumption, monotone operator theory cannot be used. Moreover, the discontinuity in the diffusion coefficient bars us from applying classical results on strong solutions. However, by directly applying a Galerkin method, we obtain uniqueness and existence of the strong form solution. These results provide the basis to study the dynamics of cells in critical states.
This article offers an advanced and novel investigation into the intricate propagation dynamics of the Belousov–Zhabotinsky system with non-local delayed interaction, which exhibits dynamical transition structure from bistable to monostable. We first solved the enduring open problem concerning the existence, uniqueness and the speed sign of the bistable travelling waves. In the monostable case, we developed and derived new results for the minimal wave speed selection, which, as an application, further improved the existing investigations on pushed and pulled wavefronts. Our results can provide new estimate to the minimal speed as well as to the determinacy of the transition parameters. Moreover, these results can be directly applied to standard localised models and delayed reaction diffusion models by choosing appropriate kernel functions.
We are interested in the law of the first passage time of an Ornstein–Uhlenbeck process to time-varying thresholds. We show that this problem is connected to the laws of the first passage time of the process to members of a two-parameter family of functional transformations of a time-varying boundary. For specific values of the parameters, these transformations appear in a realisation of a standard Ornstein–Uhlenbeck bridge. We provide three different proofs of this connection. The first is based on a similar result for Brownian motion, the second uses a generalisation of the so-called Gauss–Markov processes, and the third relies on the Lie group symmetry method. We investigate the properties of these transformations and study the algebraic and analytical properties of an involution operator which is used in constructing them. We also show that these transformations map the space of solutions of Sturm–Liouville equations into the space of solutions of the associated nonlinear ordinary differential equations. Lastly, we interpret our results through the method of images and give new examples of curves with explicit first passage time densities.
In a smoothly bounded domain $\Omega \subset \mathbb{R}^n$, $n\ge 1$, this manuscript considers the homogeneous Neumann boundary problem for the chemotaxis system
\begin{eqnarray*} \left \{ \begin{array}{l} u_t = \Delta u - \nabla \cdot (u\nabla v), \\[5pt] v_t = \Delta v + u - \alpha uv, \end{array} \right . \end{eqnarray*}
with parameter $\alpha \gt 0$ and with coincident production and uptake of attractants, as recently emphasized by Dallaston et al. as relevant for the understanding of T-cell dynamics.
It is shown that there exists $\delta _\star =\delta _\star (n)\gt 0$ such that for any given $\alpha \ge \frac{1}{\delta _\star }$ and for any suitably regular initial data satisfying $v(\cdot, 0)\le \delta _\star$, this problem admits a unique classical solution that stabilizes to the constant equilibrium $(\frac{1}{|\Omega |}\int _\Omega u(\cdot, 0), \, \frac{1}{\alpha })$ in the large time limit.
For the special case $\eta =0$, fruitful results have been achieved since Tao and Winkler's work in 2011. However, there is no any progress for the general case $\eta >0$ in the past ten years. In this paper, we analysed some commonly used research methods when $\eta =0$, and found that these methods are completely unsuitable for situations where $\eta >0$. By introducing some new forms of functionals, we reconstruct the relationship between the haptotactic term and the nonlinear diffusion term, and ultimately prove the global existence of weak solutions. This result improves and perfects a series of works previously presented in the literature.
Infection mechanism plays a significant role in epidemic models. To investigate the influence of saturation effect, a nonlocal (convolution) dispersal susceptible-infected-susceptible epidemic model with saturated incidence is considered. We first study the impact of dispersal rates and total population size on the basic reproduction number. Yang, Li and Ruan (J. Differ. Equ. 267 (2019) 2011–2051) obtained the limit of basic reproduction number as the dispersal rate tends to zero or infinity under the condition that a corresponding weighted eigenvalue problem has a unique positive principal eigenvalue. We remove this additional condition by a different method, which enables us to reduce the problem on the limiting profile of the basic reproduction number into that of the spectral bound of the corresponding operator. Then we establish the existence and uniqueness of endemic steady states by a equivalent equation and finally investigate the asymptotic profiles of the endemic steady states for small and large diffusion rates to provide reference for disease prevention and control, in which the lack of regularity of the endemic steady state and Harnack inequality makes the limit function of the sequence of the endemic steady state hard to get. Finally, we find whether lowing the movements of susceptible individuals can eradicate the disease or not depends on not only the sign of the difference between the transmission rate and the recovery rate but also the total population size, which is different from that of the model with standard or bilinear incidence.
This paper investigates the separation property in binary phase-segregation processes modelled by Cahn-Hilliard type equations with constant mobility, singular entropy densities and different particle interactions. Under general assumptions on the entropy potential, we prove the strict separation property in both two and three-space dimensions. Namely, in 2D, we notably extend the minimal assumptions on the potential adopted so far in the literature, by only requiring a mild growth condition of its first derivative near the singular points $\pm 1$, without any pointwise additional assumption on its second derivative. For all cases, we provide a compact proof using De Giorgi’s iterations. In 3D, we also extend the validity of the asymptotic strict separation property to the case of fractional Cahn-Hilliard equation, as well as show the validity of the separation when the initial datum is close to an ‘energy minimizer’. Our framework offers insights into statistical factors like particle interactions, entropy choices and correlations governing separation, with broad applicability.
Flowering plants depend on some animals for pollination and contribute to nourish the animals in natural environments. We call these animals pollinators and build a plants-pollinators cooperative model with impulsive effect on a periodically evolving domain. Next, we define the ecological reproduction index for single plant model and plants-pollinators system, respectively, whose threshold dynamics, including the extinction, persistence and coexistence, is established by the method of upper and lower solutions. Theoretical analysis shows that a large domain evolution rate has a positive influence on the survival of pollinators whether or not the impulsive effect occurs, and the pulse eliminates the pollinators even when the evolution rate is high. Moreover, some selective numerical simulations are still performed to explain our theoretical results.
in a bounded domain $\Omega \subset \mathbb {R}^N(N=3,\,4,\,5)$ with smooth boundary $\partial \Omega$. It is shown that if $m>\max \{1,\,\frac {3N-2}{2N+2}\}$, for any reasonably smooth nonnegative initial data, the corresponding no-flux type initial-boundary value problem possesses a globally bounded weak solution. Furthermore, we prove that the solution converges to the spatially homogeneous equilibrium $(\bar {u}_0,\,0)$ in an appropriate sense as $t\rightarrow \infty$, where $\bar {u}_0=\frac {1}{|\Omega |}\int _\Omega u_0$. This result not only partly extends the previous global boundedness result in Fan and Jin (J. Math. Phys.58 (2017), 011503) and Wang and Xiang (Z. Angew. Math. Phys.66 (2015), 3159–3179) to $m>\frac {3N-2}{2N}$ in the case $N\geq 3$, but also partly improves the global existence result in Zheng and Wang (Discrete Contin. Dyn. Syst. Ser. B22 (2017), 669–686) to $m>\frac {3N}{2N+2}$ when $N\geq 2$.
Existence of specific eternal solutions in exponential self-similar form to the following quasilinear diffusion equation with strong absorption
\[ \partial_t u=\Delta u^m-|x|^{\sigma}u^q, \]
posed for $(t,\,x)\in (0,\,\infty )\times \mathbb {R}^N$, with $m>1$, $q\in (0,\,1)$ and $\sigma =\sigma _c:=2(1-q)/ (m-1)$ is proved. Looking for radially symmetric solutions of the form
we show that there exists a unique exponent $\beta ^*\in (0,\,\infty )$ for which there exists a one-parameter family $(u_A)_{A>0}$ of solutions with compactly supported and non-increasing profiles $(f_A)_{A>0}$ satisfying $f_A(0)=A$ and $f_A'(0)=0$. An important feature of these solutions is that they are bounded and do not vanish in finite time, a phenomenon which is known to take place for all non-negative bounded solutions when $\sigma \in (0,\,\sigma _c)$.
For $s\in [\tfrac {1}{2},\, 1)$, let $u$ solve $(\partial _t - \Delta )^s u = Vu$ in $\mathbb {R}^{n} \times [-T,\, 0]$ for some $T>0$ where $||V||_{ C^2(\mathbb {R}^n \times [-T, 0])} < \infty$. We show that if for some $0<\mathfrak {K} < T$ and $\epsilon >0$
We analyse the asymptotic dynamics of quasilinear parabolic equations when solutions may grow up (i.e. blow up in infinite time). For such models, there is a global attractor which is unbounded and the semiflow induces a nonlinear dynamics at infinity by means of a Poincaré projection. In case the dynamics at infinity is given by a semilinear equation, then it is gradient, consisting of the so-called equilibria at infinity and their corresponding heteroclinics. Moreover, the diffusion and reaction compete for the dimensionality of the induced dynamics at infinity. If the equilibria are hyperbolic, we explicitly prove the occurrence of heteroclinics between bounded equilibria and/or equilibria at infinity. These unbounded global attractors describe the space of admissible initial data at event horizons of certain black holes.
In this paper, we analyse Turing instability and bifurcations in a host–parasitoid model with nonlocal effect. For a ordinary differential equation model, we provide some preliminary analysis on Hopf bifurcation. For a reaction–diffusion model with local intraspecific prey competition, we first explore the Turing instability of spatially homogeneous steady states. Next, we show that the model can undergo Hopf bifurcation and Turing–Hopf bifurcation, and find that a pair of spatially nonhomogeneous periodic solutions is stable for a (8,0)-mode Turing–Hopf bifurcation and unstable for a (3,0)-mode Turing–Hopf bifurcation. For a reaction–diffusion model with nonlocal intraspecific prey competition, we study the existence of the Hopf bifurcation, double-Hopf bifurcation, Turing bifurcation, and Turing–Hopf bifurcation successively, and find that a spatially nonhomogeneous quasi-periodic solution is unstable for a (0,1)-mode double-Hopf bifurcation. Our results indicate that the model exhibits complex pattern formations, including transient states, monostability, bistability, and tristability. Finally, numerical simulations are provided to illustrate complex dynamics and verify our theoretical results.
We investigate an inverse boundary value problem of determination of a nonlinear law for reaction-diffusion processes, which are modeled by general form semilinear parabolic equations. We do not assume that any solutions to these equations are known a priori, in which case the problem has a well-known gauge symmetry. We determine, under additional assumptions, the semilinear term up to this symmetry in a time-dependent anisotropic case modeled on Riemannian manifolds, and for partial data measurements on ${\mathbb R}^n$.
Moreover, we present cases where it is possible to exploit the nonlinear interaction to break the gauge symmetry. This leads to full determination results of the nonlinear term. As an application, we show that it is possible to give a full resolution to classes of inverse source problems of determining a source term and nonlinear terms simultaneously. This is in strict contrast to inverse source problems for corresponding linear equations, which always have the gauge symmetry. We also consider a Carleman estimate with boundary terms based on intrinsic properties of parabolic equations.
Conventional preytaxis systems assume that prey-tactic velocity is proportional to the prey density gradient. However, many experiments exploring the predator–prey interactions show that it is the predator’s acceleration instead of velocity that is proportional to the prey density gradient in the prey-tactic movement, which we call preytaxis with prey-induced acceleration. Mathematical models of preytaxis with prey-induced acceleration were proposed by Arditi et al. ((2001) Theor. Popul. Biol. 59(3), 207–221) and Sapoukhina et al. ((2003) Am. Nat. 162(1), 61–76) to interpret the spatial heterogeneity of predators and prey observed in experiments. This paper is devoted to exploring the qualitative behaviour of such preytaxis systems with prey-induced acceleration and establishing the global existence of classical solutions with uniform-in-time bounds in all spatial dimensions. Moreover, we prove the global stability of spatially homogeneous prey-only and coexistence steady states with decay rates under certain conditions on system parameters. For the parameters outside the stability regime, we perform linear stability analysis to find the possible patterning regimes and use numerical simulations to demonstrate that spatially inhomogeneous time-periodic patterns will typically arise from the preytaxis system with prey-induced acceleration. Noticing that conventional preytaxis systems are unable to produce spatial patterns, our results imply that the preytaxis with prey-induced acceleration is indeed more appropriate than conventional preytaxis to interpret the spatial heterogeneity resulting from predator–prey interactions.
In this paper, we consider reaction-diffusion epidemic models with mass action or standard incidence mechanism and study the impact of limiting population movement on disease transmissions. We set either the dispersal rate of the susceptible or infected people to zero and study the corresponding degenerate reaction-diffusion model. Our main approach to study the global dynamics of these models is to construct delicate Lyapunov functions. Our results show that the consequences of limiting the movement of susceptible or infected people depend on transmission mechanisms, model parameters and population size.