Comparison of Some Partial Differential Equation Models of Flexible Structures *

1987 ◽  
Vol 20 (1) ◽  
pp. 287-292 ◽  
Author(s):  
J. Bontsema ◽  
R.F. Curtain ◽  
J.M. Schumacher
Author(s):  
Michael Doebeli

This chapter discusses partial differential equation models. Partial differential equations can describe the dynamics of phenotype distributions of polymorphic populations, and they allow for a mathematically concise formulation from which some analytical insights can be obtained. It has been argued that because partial differential equations can describe polymorphic populations, results from such models are fundamentally different from those obtained using adaptive dynamics. In partial differential equation models, diversification manifests itself as pattern formation in phenotype distribution. More precisely, diversification occurs when phenotype distributions become multimodal, with the different modes corresponding to phenotypic clusters, or to species in sexual models. Such pattern formation occurs in partial differential equation models for competitive as well as for predator–prey interactions.


Mathematics ◽  
2020 ◽  
Vol 8 (9) ◽  
pp. 1483
Author(s):  
Alexander Churkin ◽  
Stephanie Lewkiewicz ◽  
Vladimir Reinharz ◽  
Harel Dahari ◽  
Danny Barash

Parameter estimation in mathematical models that are based on differential equations is known to be of fundamental importance. For sophisticated models such as age-structured models that simulate biological agents, parameter estimation that addresses all cases of data points available presents a formidable challenge and efficiency considerations need to be employed in order for the method to become practical. In the case of age-structured models of viral hepatitis dynamics under antiviral treatment that deal with partial differential equations, a fully numerical parameter estimation method was developed that does not require an analytical approximation of the solution to the multiscale model equations, avoiding the necessity to derive the long-term approximation for each model. However, the method is considerably slow because of precision problems in estimating derivatives with respect to the parameters near their boundary values, making it almost impractical for general use. In order to overcome this limitation, two steps have been taken that significantly reduce the running time by orders of magnitude and thereby lead to a practical method. First, constrained optimization is used, letting the user add constraints relating to the boundary values of each parameter before the method is executed. Second, optimization is performed by derivative-free methods, eliminating the need to evaluate expensive numerical derivative approximations. The newly efficient methods that were developed as a result of the above approach are described for hepatitis C virus kinetic models during antiviral therapy. Illustrations are provided using a user-friendly simulator that incorporates the efficient methods for both the ordinary and partial differential equation models.


2013 ◽  
Vol 108 (503) ◽  
pp. 1009-1020 ◽  
Author(s):  
Xiaolei Xun ◽  
Jiguo Cao ◽  
Bani Mallick ◽  
Arnab Maity ◽  
Raymond J. Carroll

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