Abstract

The observation of critical-like behavior in cortical networks represents a major step forward in elucidating how the brain manages information. Understanding the origin and functionality of critical-like dynamics, as well as its robustness, is a major challenge in contemporary neuroscience. Here, we present an extensive numerical study of a family of simple dynamical models, which describe activity propagation in brain networks through the integration of different neighboring spiking potentials, mimicking basic neural interactions. The requirement of signal integration may lead to discontinuous phase transitions in networks that are well described by the mean-field approximation, thus preventing the emergence of critical points in such systems. Brain networks, however, are finite dimensional and exhibit a heterogeneous hierarchical structure that cannot be encoded in mean-field models. Here we propose that, as a consequence of the presence of such a heterogeneous substrate with its concomitant structural disorder, critical-like features may emerge even in the presence of integration. These conclusions may prove significant in explaining the observation of traits of critical behavior in large-scale measurements of brain activity.

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