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Halvor Herlyng

Publications and source records attributed to Halvor Herlyng.

3 recordsLinked to original sources

Characterization of coherent flow structures in brain ventricles

The dynamic flow of cerebrospinal fluid (CSF) in brain ventricles exhibits flow features on several scales, both spatially and temporally. Most analysis of this complex flow and the accompanying transport has used instantaneous (Eulerian) flow variables. Such analysis makes understanding of unsteady transport challenging. Here, we analyze brain ventricular CSF flow both in a Eulerian sense and from the Lagrangian perspective -- a time-integrated view of the flow. With geometries generated from imaging data, we model CSF flow in adult human and embryonic zebrafish brain ventricles. In the human brain we model flow governed by cardiovascular pulsations, CSF secretion and motile cilia. The flow driven by cardiovascular pulsations is derived from a damped linear elastic model of brain ventricle deformations, as a result of applying displacement boundary conditions derived from experimental data. In the zebrafish brain we consider flow driven solely by motile cilia. The tissue and flow models are implemented and solved with finite element methods. We use the resulting velocity fields to compute finite-time Lyapunov exponent (FTLE) fields and use these fields to characterize Lagrangian coherent structures, which can be approximated by ridges in the FTLE fields. These coherent structures demonstrate prominent flow features in the brain ventricles congruent with findings in experimental research. In the human brain ventricles, we also investigate the role of inertia by comparing flow models governed by the Navier-Stokes and the Stokes equations. Comparisons show that solving the Stokes equations is adequate to compute integrated flow variables like stroke volumes, but that the Stokes approximation fails to resolve intricate features of flow and advective transport that are present in the solution to the Navier-Stokes equations, features that could be important to elucidating transport.

physics.flu-dyn

Modeling and simulation of electrodiffusion in dense reconstructions of cerebral tissue

Excitable tissue is fundamental to brain function, yet its study is complicated by extreme morphological complexity and the physiological processes governing its dynamics. Consequently, detailed computational modeling of this tissue represents a formidable task, requiring both efficient numerical methods and robust implementations. Meanwhile, efficient and robust methods for image segmentation and meshing are needed to provide realistic geometries for which numerical solutions are tractable. Here, we present a computational framework that models electrodiffusion in excitable cerebral tissue, together with realistic geometries generated from electron microscopy data. To demonstrate a possible application of the framework, we simulate electrodiffusive dynamics in cerebral tissue during neuronal activity. Our results and findings highlight the numerical and computational challenges associated with modeling and simulation of electrodiffusion and other multiphysics in dense reconstructions of cerebral tissue.

physics.med-ph

Scalable approximation and solvers for ionic electrodiffusion in cellular geometries

The activity and dynamics of excitable cells are fundamentally regulated and moderated by extracellular and intracellular ion concentrations and their electric potentials. The increasing availability of dense reconstructions of excitable tissue at extreme geometric detail pose a new and clear scientific computing challenge for computational modelling of ion dynamics and transport. In this paper, we design, develop and evaluate a scalable numerical algorithm for solving the time-dependent and nonlinear KNP-EMI equations describing ionic electrodiffusion for excitable cells with an explicit geometric representation of intracellular and extracellular compartments and interior interfaces. We also introduce and specify a set of model scenarios of increasing complexity suitable for benchmarking. Our solution strategy is based on an implicit-explicit discretization and linearization in time, a mixed finite element discretization of ion concentrations and electric potentials in intracellular and extracellular domains, and an algebraic multigrid-based, inexact block-diagonal preconditioner for GMRES. Numerical experiments with up to $10^8$ unknowns per time step and up to 256 cores demonstrate that this solution strategy is robust and scalable with respect to the problem size, time discretization and number of cores.

math.NA