Resources
Authors & Affiliations
Jacob Crosser, Braden A W Brinkman
Abstract
The critical brain hypothesis proposes that neural networks operate near criticality to reap the
computational benefits of accessing a wide range of timescales [1]. Proponents of this viewpoint highlight
the presence of heavy-tailed (power-law) spatiotemporal correlations as markers of criticality in the brain
[2]. Critics of this hypothesis argue that such correlations could be inherited from upstream sources, such
as sensory input [3]. Similarly, Ref. [4] constructed a model of independent neurons driven by shared
noise input that exhibited neural activity with power-law tails, which could be interpreted as introducing
an infinite correlation range inherited by otherwise independent neurons. Determining whether the brain
is critical thus demands a way to distinguish intrinsically generated criticality from heavy-tailed input
correlations inherited from upstream input.
We derive a mean-field theory to investigate the related effects of intrinsic criticality and heavy-tailed
inputs using a model of spiking neural activity driven by external noise (Fig. 1.A) in which the spiking
network and the noise process can be tuned independently to a critical state (Fig. 1.A-B). In the networks we
consider these critical states correspond to the boundary at which a single steady firing rate state becomes
unstable to self-sustaining low- or high-activity states. We show that the autocovariance of spiking activity
is heavy-tailed when the input is critical, irrespective of the degree of criticality in the network (Fig. 1.C,
main panels). Conversely, the response functions of the network---measured as the network response to a
current impulse averaged across trials---are only heavy-tailed if the spiking network is tuned to criticality
(Fig. 1.C, insets). These causal responses of neurons to membrane perturbation are independent of the
input, rendering the criticality of the input irrelevant. Our work thus suggests experimentally observed
response functions can disambiguate intrinsic versus inherited criticality in spiking neural networks.