NEW INTERIOR PENALTY DISCONTINUOUS GALERKIN METHODS FOR THE KELLER-SEGEL CHEMOTAXIS MODEL

被引:68
|
作者
Epshteyn, Yekaterina [1 ]
Kurganov, Alexander [2 ]
机构
[1] Carnegie Mellon Univ, Dept Math Sci, Pittsburgh, PA 15213 USA
[2] Tulane Univ, Dept Math, New Orleans, LA 70118 USA
关键词
Keller-Segel chemotaxis model; convection-diffusion-reaction systems; discontinuous Galerkin methods; nonsymmetric interior penalty Galerkin; incomplete interior penalty Galerkin; and symmetric interior penalty Galerkin methods; Cartesian meshes;
D O I
10.1137/07070423X
中图分类号
O29 [应用数学];
学科分类号
070104 ;
摘要
We develop a family of new interior penalty discontinuous Galerkin methods for the Keller-Segel chemotaxis model. This model is described by a system of two nonlinear PDEs: a convection-diffusion equation for the cell density coupled with a reaction-diffusion equation for the chemoattractant concentration. It has been recently shown that the convective part of this system is of a mixed hyperbolic-elliptic-type, which may cause severe instabilities when the studied system is solved by straightforward numerical methods. Therefore, the first step in the derivation of our new methods is made by introducing the new variable for the gradient of the chemoattractant concentration and by reformulating the original Keller-Segel model in the form of a convection-diffusion-reaction system with a hyperbolic convective part. We then design interior penalty discontinuous Galerkin methods for the rewritten Keller-Segel system. Our methods employ the central-upwind numerical fluxes, originally developed in the context of finite-volume methods for hyperbolic systems of conservation laws. In this paper, we consider Cartesian grids and prove error estimates for the proposed high-order discontinuous Galerkin methods. Our proof is valid for pre-blow-up times since we assume boundedness of the exact solution. We also show that the blow-up time of the exact solution is bounded from above by the blow-up time of our numerical solution. In the numerical tests presented below, we demonstrate that the obtained numerical solutions have no negative values and are oscillation-free, even though no slope-limiting technique has been implemented.
引用
收藏
页码:386 / 408
页数:23
相关论文
共 50 条
  • [31] The fractional Keller-Segel model
    Escudero, Carlos
    NONLINEARITY, 2006, 19 (12) : 2909 - 2918
  • [32] Asymptotic behaviour of solutions to the Keller-Segel model for chemotaxis with prevention of overcrowding
    Guo, Haojie
    Zheng, Sining
    Liang, Bo
    NONLINEARITY, 2013, 26 (02) : 405 - 416
  • [33] Coupled lattice Boltzmann method for generalized Keller-Segel chemotaxis model
    Yang, Xuguang
    Shi, Baochang
    Chai, Zhenhua
    COMPUTERS & MATHEMATICS WITH APPLICATIONS, 2014, 68 (12) : 1653 - 1670
  • [34] The nonsymmetric case of the Keller-Segel model in chemotaxis: some recent results
    Dirk Horstmann
    Nonlinear Differential Equations and Applications NoDEA, 2001, 8 : 399 - 423
  • [35] Beyond the Keller-Segel model
    Romanczuk, P.
    Erdmann, U.
    Engel, H.
    Schimansky-Geier, L.
    EUROPEAN PHYSICAL JOURNAL-SPECIAL TOPICS, 2008, 157 : 61 - 77
  • [36] Stability of spiky solution of Keller-Segel's minimal chemotaxis model
    Chen, Xinfu
    Hao, Jianghao
    Wang, Xuefeng
    Wu, Yaping
    Zhang, Yajing
    JOURNAL OF DIFFERENTIAL EQUATIONS, 2014, 257 (09) : 3102 - 3134
  • [37] On spectra of linearized operators for Keller-Segel models of chemotaxis
    Dejak, S. I.
    Lushnikov, P. M.
    Ovchinnikov, Yu N.
    Sigal, I. M.
    PHYSICA D-NONLINEAR PHENOMENA, 2012, 241 (15) : 1245 - 1254
  • [38] A new analysis for the Keller-Segel model of fractional order
    Kumar, Sunil
    Kumar, Amit
    Argyros, Ioannis K.
    NUMERICAL ALGORITHMS, 2017, 75 (01) : 213 - 228
  • [39] CHEMOTAXIS AND CHEMOKINESIS IN EUKARYOTIC CELLS - THE KELLER-SEGEL EQUATIONS AS AN APPROXIMATION TO A DETAILED MODEL
    SHERRATT, JA
    BULLETIN OF MATHEMATICAL BIOLOGY, 1994, 56 (01) : 129 - 146
  • [40] Chemotactic collapse for the Keller-Segel model
    Herrero, MA
    Velazquez, JJL
    JOURNAL OF MATHEMATICAL BIOLOGY, 1996, 35 (02) : 177 - 194