Chaotic Dynamics and Bifurcation Analysis of the Hindmarsh-Rose Neuron Model with Blue-Sky Catastrophe under Magnetic Field Influence
Ram Pravesh Yadav, Hirdesh K. Pharasi, R. K. Brojen Singh, Anirban Chakraborti
TL;DR
This study shows that adding a magnetic-flux feedback to the Hindmarsh–Rose neuron model with a blue-sky catastrophe reshapes its bifurcation landscape and firing patterns. By exploring two forms of nonlinear magnetic coupling and employing ISI bifurcation diagrams, phase-space analysis, Poincaré sections, and the largest Lyapunov exponent $\lambda_{\max}$, the work reveals a nonmonotonic influence of coupling strength: weak coupling preserves intrinsic spiking–bursting transitions, intermediate coupling induces chaotic bursting, and strong coupling yields structured irregular dynamics. The findings demonstrate robust qualitative behavior across coupling forms and highlight electromagnetic feedback as a tunable mechanism to control instability and chaos in slow–fast neuronal systems. This has potential implications for understanding EM field effects in neural excitability and for designing neuromodulation strategies.
Abstract
We investigate the impact of magnetic-field-induced feedback on the dynamics of a Hindmarsh-Rose neuron model exhibiting a blue-sky catastrophe. By introducing a magnetic flux variable that couples nonlinearly to the membrane potential, we demonstrate that electromagnetic effects profoundly reshape neuronal firing patterns and bifurcation structure. Interspike-interval bifurcation analysis reveals a nonmonotonic dependence on the magnetic coupling strength, with weak coupling preserving regular spiking and bursting, intermediate coupling promoting chaotic bursting, and strong coupling yielding structured irregular dynamics. These transitions are quantitatively characterized using the largest Lyapunov exponent computed via the Wolf algorithm and supported by Poincaré sections and time-series analysis. Our results establish electromagnetic feedback as a robust and tunable mechanism for controlling instability and chaos in slow-fast neuronal systems.
