Multi-band oscillations emerge from a simple spiking network

TL;DR

This paper demonstrates that multi-band neuronal oscillations can emerge from a simple excitatory-inhibitory network driven by constant input, revealing a geometric bifurcation mechanism without complex inputs or multiple timescales.

Contribution

It introduces a novel theoretical framework showing how multi-band oscillations arise from basic network interactions through bifurcations, using reduced models and Poincaré sections.

Findings

Multi-band oscillations emerge from simple networks with constant input.

A geometric bifurcation mechanism explains multi-band dynamics.

Reduced models capture the core bifurcation behavior.

Abstract

In the brain, coherent neuronal activities often appear simultaneously in multiple frequency bands, e.g., as combinations of alpha (8-12 Hz), beta (12.5-30 Hz), gamma (30-120 Hz) oscillations, among others. These rhythms are believed to underlie information processing and cognitive functions and have been subjected to intense experimental and theoretical scrutiny. Computational modeling has provided a framework for the emergence of network-level oscillatory behavior from the interaction of spiking neurons. However, due to the strong nonlinear interactions between highly recurrent spiking populations, the interplay between cortical rhythms in multiple frequency bands has rarely been theoretically investigated. Many studies invoke multiple physiological timescales or oscillatory inputs to produce rhythms in multi-bands. Here we demonstrate the emergence of multi-band oscillations in a simple network consisting of one excitatory and one inhibitory neuronal population driven by constant input. First, we construct a data-driven, Poincar\'e section theory for robust numerical observations of single-frequency oscillations bifurcating into multiple bands. Then we develop model reductions of the stochastic, nonlinear, high-dimensional neuronal network to capture the appearance of multi-band dynamics and the underlying bifurcations theoretically. Furthermore, when viewed within the reduced state space, our analysis reveals conserved geometrical features of the bifurcations on low-dimensional dynamical manifolds. These results suggest a simple geometric mechanism behind the emergence of multi-band oscillations without appealing to oscillatory inputs or multiple synaptic or neuronal timescales. Thus our work points to unexplored regimes of stochastic competition between excitation and inhibition behind the generation of dynamic, patterned neuronal activities.