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Based on some elementary estimates for the space-time derivatives of the heat kernel, we use a bootstrapping approach to establish the optimal decay rates for the $L^q(mathbb{R}^d)$ ($1leq qleqinfty$, $dinmathbb{N}$) norm of the space-time derivatives of solutions to the (modified) Patlak-Keller-Segel equations with initial data in $L^1(mathbb{R}^d)$, which implies the joint space-time analyticity of solutions. When the $L^1(mathbb{R}^d)$ norm of the initial datum is small, the upper bound for the decay estimates is global in time, which yields a lower bound on the growth rate of the radius of space-time analyticity in time. As a byproduct, the space analyticity is obtained for any initial data in $L^1(mathbb{R}^d)$. The decay estimates and space-time analyticity are also established for solutions bounded in both space and time variables. The results can be extended to a more general class of equations, including the Navier-Stokes equations.
We study the regularity and large-time behavior of a crowd of species driven by chemo-tactic interactions. What distinguishes the different species is the way they interact with the rest of the crowd: the collective motion is driven by different chem
Perhaps the most classical diffusion model for chemotaxis is the Patlak-Keller-Segel system begin{equation} label{ks0} left{ begin{aligned} u_t =& Delta u - abla cdot(u abla v) quad inn R^2times(0,infty), v =& (-Delta_{R^2})^{-1} u := frac 1{2pi}
In this paper, we proposed a coupled Patlak-Keller-Segel-Navier-Stokes system, which has dissipative free energy. On the plane $rr^2$, if the total mass of the cells is strictly less than $8pi$, classical solutions exist for any finite time, and thei
We address the analyticity and large time decay rates for strong solutions of the Hall-MHD equations. By Gevrey estimates, we show that the strong solution with small initial date in $H^r(mathbb{R}^3)$ with $r>f 52$ becomes analytic immediately after
We show that the Keller-Segel model in one dimension with Neumann boundary conditions and quadratic cellular diffusion has an intricate phase transition diagram depending on the chemosensitivity strength. Explicit computations allow us to find a myri