We investigate a recent model proposed in the literature elucidating patterns driven by chemotaxis, similar to viscous fingering phenomena. Notably, this model incorporates a singular advection term arising from a modified formulation of Darcy’s law. It is noteworthy that this type of advection can also be well interpreted as a description of a radial fluid flow source surrounding an aggregation of cells. For the two-dimensional scenario, we establish a precise threshold delineating between blow-up and global solution existence. This threshold is contingent upon the pressure magnitude and the initial total mass of the aggregating cells.

Well-posedness in time-weighted spaces of certain quasilinear (and semilinear) parabolic evolution equations $u'=A(u)u+f(u)$ is established. The focus lies on the case of strict inclusions $\mathrm{dom}(f)\subsetneq \mathrm{dom}(A)$ of the domains of the nonlinearities $u\mapsto f(u)$ and $u\mapsto A(u)$. Based on regularizing effects of parabolic equations it is shown that a semiflow is generated in intermediate spaces. In applications this allows one to derive global existence from weaker a priori estimates. The result is illustrated by examples of chemotaxis systems.

This paper deals with a 4th-order parabolic equation involving the Frobenius norm of a Hessian matrix, subject to the Neumann boundary conditions. Some threshold results for blow-up or global or extinction solutions are obtained through classifying the initial energy and the Nehari energy. The bounds of blow-up time, decay estimates, and extinction rates are studied, respectively.

We study the global well-posedness and uniform boundedness of a two-dimensional reaction–advection–diffusion system with nonlinear advection. This strongly coupled system of nonlinear partial differential equations represents the continuum of a 2D lattice model designed to describe residential burglary, where each location is characterised by a tractability value that varies in both space and time. We show that the model with sublinear advection enhancement is globally well-posed, with a unique solution that is classical and uniformly bounded in time. Our results provide valuable insights into the development of urban crime models with nonlinear advection enhancements, making them suitable for broader applications, including nonlocal or heterogeneous near-repeat victimisation effects.

We prove the existence of solutions to the Kuramoto–Sivashinsky equation with low regularity data in function spaces based on the Wiener algebra and in pseudomeasure spaces. In any spatial dimension, we allow the data to have its antiderivative in the Wiener algebra. In one spatial dimension, we also allow data that are in a pseudomeasure space of negative order. In two spatial dimensions, we also allow data that are in a pseudomeasure space one derivative more regular than in the one-dimensional case. In the course of carrying out the existence arguments, we show a parabolic gain of regularity of the solutions as compared to the data. Subsequently, we show that the solutions are in fact analytic at any positive time in the interval of existence.

In this paper, we prove the global exstence of weak solutions for a porous medium dynamics of m species moving between two domains separated by a zero-thickness membrane. On this membrane, Kedem–Katchalsky conditions are considered, and the study is characterized by natural structural conditions applied to the nonlinear reactive terms. The global existence is established under the assumption that these reactive terms are bounded in $L^1$. This problem has already been analyzed in the linear diffusion case by Ciavolella and Perthame in Ciavolella and Perthame (2021, Journal of Evolution Equations 21, 1513–1540). The present work constitutes an extension for nonlinear diffusion, particularly of the porous medium type, in the form $\partial _t v_i - \Delta v_i^{r_i} = R_i$, for an exponent $r_i < 2$. The case $r_i \geq 2$ remains an open problem. This paper is an adaptation of the ideas from Ciavolella and Perthame (2021, Journal of Evolution Equations 21, 1513–1540), with new strategies to overcome the appearance of nonlinearity and degeneracy in the diffusion term.

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*}

$\phi *u$

$\phi (y) \equiv H\left (\frac{1}{4}-y^2\right )$

$u=1$

$D$

$\Delta _1 \approx 0.00297$

$D \ll 1$

$O(1)$

$u=O(1)$

$u$

$D \to 0^+$

$D \geq \Delta _1$

$2 \sqrt{D}$

$0 \lt D \lt \Delta _1$

$u=0$

$D$

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*}

$\alpha \gt 0$

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.

In this paper, we consider the following PDE-ODE system modelling cancer invasion with slow diffusion and ECM remodelling,

\[ \begin{cases} u_t=\Delta u^m-\chi\nabla\cdot(u\nabla v)-\xi\nabla\cdot(u\nabla\omega)+\mu u(1-u-\omega), \\ v_t=\Delta v+u-v, \\ \omega_t={-}v\omega+\eta \omega(1-u-\omega). \end{cases} \]

$\eta =0$

$\eta >0$

$\eta =0$

$\eta >0$

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.

This paper deals with the following quasilinear chemotaxis system with consumption of chemoattractant

\[ \left\{\begin{array}{@{}ll} u_t=\Delta u^{m}-\nabla\cdot(u\nabla v),\quad & x\in \Omega,\quad t>0,\\ v_t=\Delta v-uv,\quad & x\in \Omega,\quad t>0\\ \end{array}\right. \]

$\Omega \subset \mathbb {R}^N(N=3,\,4,\,5)$

$\partial \Omega$

$m>\max \{1,\,\frac {3N-2}{2N+2}\}$

$(\bar {u}_0,\,0)$

$t\rightarrow \infty$

$\bar {u}_0=\frac {1}{|\Omega |}\int _\Omega u_0$

$m>\frac {3N-2}{2N}$

$N\geq 3$

$m>\frac {3N}{2N+2}$

$N\geq 2$

Existence of specific eternal solutions in exponential self-similar form to the following quasilinear diffusion equation with strong absorption

\[ \partial_t u=\Delta u^m-|x|^{\sigma}u^q, \]

$(t,\,x)\in (0,\,\infty )\times \mathbb {R}^N$

$m>1$

$q\in (0,\,1)$

$\sigma =\sigma _c:=2(1-q)/ (m-1)$

\[ u(t,x)={\rm e}^{-\alpha t}f(|x|\,{\rm e}^{\beta t}), \quad \alpha=\frac{2}{m-1}\beta, \]

$\beta ^*\in (0,\,\infty )$

$(u_A)_{A>0}$

$(f_A)_{A>0}$

$f_A(0)=A$

$f_A'(0)=0$

$\sigma \in (0,\,\sigma _c)$