Stability, free energy and dynamics of multi-spikes in the minimal Keller-Segel model
Existence problems for PDEs: global existence, local existence, non-existence (35A01) Stability in context of PDEs (35B35) Asymptotic behavior of solutions to PDEs (35B40) Reaction-diffusion equations (35K57) PDEs in connection with biology, chemistry and other natural sciences (35Q92) Cell movement (chemotaxis, etc.) (92C17)
In this article, the authors study the stability of multi-spike steady states of the \(1\)-D Keller-Segel model \[ \begin{cases} u_t = (u_x - \kappa uv_x)_x, \quad x \in (0,L), \ t >0, \\ v_t = v_{xx} - v +u, \quad x \in (0,L), \ t >0, \\ u_x(x,t) = v_x(x,t) = 0, \quad x \in (0,L), \ t >0, \\ \int_0^L u(x,0) \ dx = M>0, \end{cases} \tag{1} \] where \(L < \infty\), \(\kappa >0\) a constant and the initial datum \(u(x,0), v(x,0)\) are assumed to be non-negative. Each steady state of (1) can be extended evenly and periodically to the whole space \(\mathbb{R}\). In [J. Differ. Equations 257, No. 9, 3102--3134 (2014; Zbl 1302.35053)] \textit{X. Chen} et al. showed that the decreasing steady states of (1) are unique if \(\kappa \gg 1\), and such steady states are locally asymptotically stable in \(H^1\)-topology. In addition, they obtained a rigorous asymptotic expansion of the solutions and prove that it is locally and exponentially stable. Such expansions are called single boundary spike. Since the steady states are monotone, by reflecting with respect to either \(L\) or \(0\) and scaling it to \((0,L)\) one gets either a double boundary spike or a single interior spike. The authors of this article showed that both the double boundary spike and single interior spike are unstable steady states. The same result holds for multi-spike steady states: for each \(n \in \mathbb{N}\) there exists only two pairs of symmetric multi-spike steady states of (1) which change sign \((n-1)\)-times in \((0,L)\), and all these steady states are unstable. Finally, the authors showed that the energy (with respect to an appropriately defined Lyapunov functional) of the interior spiked steady states increases as the number of spikes increases and the constant steady state has the highest energy compared to the spiked ones. In particular, the monotone steady states are most stable, and the constant steady states are most unstable. The authors also presented numerical simulations to illustrate and support their theoretical results.
- The stability and dynamics of a spike in the 1D Keller–Segel model
- Stability of spiky solution of Keller-Segel's minimal chemotaxis model
- Dynamics of spike in a Keller-Segel's minimal chemotaxis model
- Existence of multi-spikes in the Keller–Segel model with logistic growth
- The existence and stability of spikes in the one-dimensional Keller-Segel model with logistic growth
- The stability of the Keller-Segel model
- Instability in a generalized Keller-Segel model
- Stable dynamics of spikes in solutions to a system of reaction-diffusion equations
- Radial spiky steady states of a flux‐limited Keller–Segel model: Existence, asymptotics, and stability
- Dynamic and steady states for multi-dimensional Keller-Segel model with diffusion exponent \(m > 0\)
- A user's guide to PDE models for chemotaxis
- An eigenvalue problem arising from spiky steady states of a minimal chemotaxis model
- Basic mechanisms driving complex spike dynamics in a chemotaxis model with logistic growth
- Bifurcation from simple eigenvalues
- Boundary spike-layer solutions of the singular Keller-Segel system: existence and stability
- Boundary spikes of a Keller-Segel chemotaxis system with saturated logarithmic sensitivity
- Boundedness vs. blow-up in a chemotaxis system
- Bubbling on boundary submanifolds for the Lin-Ni-Takagi problem at higher critical exponents
- Chemotactic collapse for the Keller-Segel model
- Collapsing steady states of the Keller–Segel system
- Degree theory for C^1 Fredholm mappings of index 0
- Dynamics of spike in a Keller-Segel's minimal chemotaxis model
- Existence of multiple spike stationary patterns in a chemotaxis model with weak saturation
- Existence, uniqueness, and stability of bubble solutions of a chemotaxis model
- Global and exponential attractor of the repulsive Keller–Segel model with logarithmic sensitivity
- Global existence and convergence to steady states in a chemorepulsion system
- Global existence and steady states of a two competing species Keller-Segel chemotaxis model
- Initiation of slime mold aggregation viewed as an instability
- Large amplitude stationary solutions to a chemotaxis system
- Locating the peaks of least-energy solutions to a semilinear Neumann problem
- Model for chemotaxis
- Multipeak solutions for a semilinear Neumann problem
- Multiple interior peak solutions for some singularly perturbed Neumann problems.
- Non-local cell adhesion models. Symmetries and bifurcations in 1-D
- Nonconstant positive steady states and pattern formation of 1D prey-taxis systems
- Nonlinear aspects of chemotaxis
- On a chemotaxis model with saturated chemotactic flux
- On a repulsion Keller–Segel system with a logarithmic sensitivity
- On convergence to equilibria for the Keller-Segel chemotaxis model
- On global bifurcation for quasilinear elliptic systems on bounded domains
- On the boundary spike layer solutions to a singularly perturbed Neumann problem
- On the number of interior peak solutions for a singularly perturbed Neumann problem
- On the shape of least‐energy solutions to a semilinear Neumann problem
- Phase transitions and bump solutions of the Keller-Segel model with volume exclusion
- Qualitative analysis of a Lotka-Volterra competition system with advection
- Qualitative analysis of stationary Keller-Segel chemotaxis models with logistic growth
- Qualitative Behavior of Solutions of Chemotactic Diffusion Systems: Effects of Motility and Chemotaxis and Dynamics
- Some global results for nonlinear eigenvalue problems
- Spectral analysis for stability of bubble steady states of a Keller-Segel's minimal chemotaxis model
- Spikes and diffusion waves in a one-dimensional model of chemotaxis
- Spiky and transition layer steady states of chemotaxis systems via global bifurcation and Helly's compactness theorem
- Spiky steady states of a chemotaxis system with singular sensitivity
- Stability of spiky solution of Keller-Segel's minimal chemotaxis model
- Stationary patterns and their selection mechanism of urban crime models with heterogeneous near-repeat victimization effect
- Stationary ring and concentric-ring solutions of the Keller-Segel model with quadratic diffusion
- Stationary Solutions of Chemotaxis Systems
- The Existence and Stability of Spike Patterns in a Chemotaxis Model
- The stability and dynamics of a spike in the 1D Keller–Segel model
- Time-periodic and stable patterns of a two-competing-species Keller-Segel chemotaxis model: effect of cellular growth
- Traveling bands of chemotactic bacteria: a theoretical analysis
- Detecting minimum energy states and multi-stability in nonlocal advection-diffusion models for interacting species
- The existence and stability of spikes in the one-dimensional Keller-Segel model with logistic growth
- Pattern formation in Keller-Segel chemotaxis models with logistic growth
- The stability and dynamics of a spike in the 1D Keller–Segel model
- Classification and stability of global inhomogeneous solutions of a macroscopic model of cell motion
- Existence and Stability of Localized Patterns in the Population Models with Large Advection and Strong Allee Effect
- Stability, bifurcation and spikes of stationary solutions in a chemotaxis system with singular sensitivity and logistic source
- Boundary and interior spikes in economic agglomeration of a spatial Solow model with capital-induced labor migration
- Pattern formation in a spatial public goods dilemma due to diffusive or directed motion
- Stability of spiky solution of Keller-Segel's minimal chemotaxis model
This page was built for publication: Stability, free energy and dynamics of multi-spikes in the minimal Keller-Segel model
Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q2131192)