Wave-driven phase wave patterns in a ring of FitzHugh-Nagumo oscillators
Daniel Cebrián-Lacasa, Marcin Leda, Andrew B. Goryachev, Lendert Gelens
TL;DR
This work introduces a two-field FitzHugh-Nagumo model comprising a cytoplasmic disc driving a cortical ring via unidirectional coupling to study wave-driven phase patterns. By varying the coupling strength, diffusion, and driving pulses, it identifies three external-regime outcomes—oscillatory, excitable, and non-excitable—each producing distinct phase-wave phenomena; a reduced linear-phase oscillator analysis links these patterns to driving pulse width and speed, yielding a phase-wavelength relation $\lambda = vT$. The findings illuminate how diffusion and pacemaker-driven waves shape cortical-like dynamics, offering a framework applicable to cellular signaling and other excitable-media contexts, and suggesting extensions to 3D or heterogeneous systems where spiral-turbulence may arise. Overall, the study demonstrates that phase patterns, traveling pulses, and connective-pulse phenomena emerge from simple unidirectional coupling and diffusion under a pacemaker-driven regime, with broad implications for interpreting wave-like activity in biology and beyond.
Abstract
We explore a biomimetic model that simulates a cell, with the internal cytoplasm represented by a two-dimensional circular domain and the external cortex by a surrounding ring, both modeled using FitzHugh-Nagumo systems. The external ring is dynamically influenced by a pacemaker-driven wave originating from the internal domain, leading to the emergence of three distinct dynamical states based on the varying strengths of coupling. The range of dynamics observed includes phase patterning, the propagation of phase waves, and interactions between traveling and phase waves. A simplified linear model effectively explains the mechanisms behind the variety of phase patterns observed, providing insights into the complex interplay between a cell's internal and external environments.
