Data-driven inference of brain dynamical states from the r-spectrum of correlation matrices
Christopher Gabaldon, Adria Mulero, Rong Wang, Daniel A. Martin, Sabrina Camargo, Qian-Yuan Tang, Ignacio Cifre, Changsong Zhou, Dante R. Chialvo
TL;DR
The paper addresses the loss of dynamical information when using fixed correlation thresholds by introducing the r-spectrum, which treats the threshold r as a control parameter and identifies a characteristic percolation point r_c where multiple independent signatures converge. Through analysis of resting-state fMRI from N=996 healthy individuals and simulations with a whole-brain GH model, the framework shows r_c covaries with temporal autocorrelation AC(1) and tracks proximity to criticality; the model results further demonstrate r_c moving with the control parameter T near the critical point. The study also demonstrates robustness across modeling choices by testing alternative r_c definitions and shows percolation-based observables (S_2, σS_1, L(G)) converge at r_c, linking spatial organization to dynamical state. Overall, the r-spectrum provides a threshold-free, physically grounded method to compare brain dynamical states and relate them to aging, integration–segregation spectra, and critical dynamics.
Abstract
We present a data-driven framework to characterize large-scale brain dynamical states directly from correlation matrices at the single-subject level. By treating correlation thresholding as a percolation-like probe of connectivity, the approach tracks multiple cluster- and network-level observables and identifies a characteristic percolation threshold, rc, at which these signatures converge. We use $r_c$ as an operational and physically interpretable descriptor of large-scale brain dynamical state. Applied to resting-state fMRI data from a large cohort of healthy individuals (N = 996), the method yields stable, subject-specific estimates that covary systematically with established dynamical indicators such as temporal autocorrelations. Numerical simulations of a whole-brain model with a known critical regime further show that $r_c$ tracks changes in collective dynamics under controlled variations of excitability. By replacing arbitrary threshold selection with a criterion intrinsic to correlation structure, the r-spectra provides a physically grounded approach for comparing brain dynamical states across individuals.
