Alpha-Delta Transitions in Cortical Rhythms as grazing bifurcations
Huda Mahdi, Jan Sieber, Krasimira Tsaneva-Atanasova
TL;DR
The paper addresses how alpha and delta cortical rhythms emerge and transition within the Jansen–Rit neural mass framework. It develops a singular perturbation analysis by nondimensionalising the model and introducing a small parameter $ obreakoldsymbol{\e}$, enabling a piecewise-smooth, grazing mechanism to explain the alpha–delta transition. The main result is that the alpha-to-delta boundary corresponds to a grazing bifurcation of alpha-type periodic orbits in the singular limit, with explicit two-parameter mappings in $(b^*,G)$ that align with Hopf and SNIC structures. This provides a mechanistic, analytic explanation for rhythm switching in cortical activity, clarifying the nature of previously labeled “false bifurcations” and offering predictive boundaries for transitions under parameter variations and nonzero inputs.
Abstract
The Jansen-Rit model of a cortical column in the cerebral cortex is widely used to simulate spontaneous brain activity (EEG) and event-related potentials. It couples a pyramidal cell population with two interneuron populations, of which one is fast and excitatory and the other slow and inhibitory. Our paper studies the transition between alpha and delta oscillations produced by the model. Delta oscillations are slower than alpha oscillations and have a more complex relaxation-type time profile. In the context of neuronal population activation dynamics, a small threshold means that neurons begin to activate with small input or stimulus, indicating high sensitivity to incoming signals. A steep slope signifies that activation increases sharply as input crosses the threshold. Accordingly in the model the excitatory activation thresholds are small and the slopes are steep. Hence, a singular limit replacing the excitatory activation function with all-or-nothing switches, eg. a Heaviside function, is appropriate. In this limit we identify the transition between alpha and delta oscillations as a discontinuity-induced grazing bifurcation. At the grazing the minimum of the pyramidal-cell output equals the threshold for switching off the excitatory interneuron population, leading to a collapse in excitatory feedback.
