where p > 1. 1 < p < 2 is called the fast p-Laplacian diffusion, while p > 2 is called the slow p-Laplacian diffusion. Especially, the p-Laplacian Keller-Segel model turns to the original model when p = 2.The Keller-Segel model was firstly presented in 1970 to describe the chemotaxis of cellular slime molds [13, 14]. The original model was considered in 2D,

Consider the following elliptic system: \begin{equation*} \left\{\aligned&-\ve^2\Delta u_1+\lambda_1u_1=\mu_1u_1^3+\alpha_1u_1^{p-1}+\beta u_2^2u_1\quad&\text{in }\Omega,\\ &-\ve^2\Delta u_2+\lambda_2u_2=\mu_2u_2^3+\alpha_2u_2^{p-1}+\beta u_1^2u_2\quad&\text{in }\Omega,\\ &u_1,u_2>0\quad\text{in }\Omega,\quad u_1=u_2=0\quad\text{on }\partial\Omega,\endaligned\right. \end{equation*} where $\Omega\subset\bbr^4$ is a bounded domain, $\lambda_i,\mu_i,\alpha_i>0$ $(i=1,2)$ and $\beta\not=0$ are constants, $\ve>0$ is a small parameter and $2<p<2^*=4$. By using variational methods, we study the existence of ground state solutions to this system for sufficiently small $\ve>0$. The concentration behaviors of least-energy solutions as $\ve\to0^+$ are also studied. Furthermore, by combining elliptic estimates and local energy estimates, we obtain the locations of these spikes as $\ve\to0^+$.

Given a compact Riemannian manifold $M$, we consider a warped product manifold $\bar M = I \times_h M$, where $I$ is an open interval in $\Bbb R$. For a positive function $\psi$ defined on $\bar M$, we generalize the arguments in \cite{GRW2015} and \cite{RW16}, to obtain the curvature estimates for Hessian equations $\sigma_k(\kappa)=\psi(V,\nu(V))$. We also obtain some existence results for the starshaped compact hypersurface $\Sigma$ satisfying the above equation with various assumptions.

The paper aims at analytically exhibiting for the first time the fundamental mechanisms underlying the fact that effective biological tissue electrical properties and their frequency dependence reflect the tissue composition and physiology. For doing so, a homogenization theory is derived to describe the effective admittivity of cell suspensions. A new formula is reported for dilute cases that gives the frequency-dependent effective admittivity with re- spect to the membrane polarization. Different microstructures are shown to be distinguish- able via spectroscopic measurements of the overall admittivity using the spectral properties of the membrane polarization. The Debye relaxation times associated with the membrane polarization tensor are shown to be able to give the microscopic structure of the medium. A natural measure of the admittivity anisotropy is introduced and its dependence on the frequency of applied current is derived. A Maxwell-Wagner-Fricke formula is given for concentric circular cells, and the results can be extended to the random cases. A randomly deformed periodic medium is also considered and a new formula is derived for the overall admittivity of a dilute suspension of randomly deformed cells.

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