Endogenous brain activity supports spontaneous human thought and shapes perception and behavior. Connectivity-based analyses of endogenous, or resting-state, functional magnetic resonance imaging (fMRI) data have revealed the existence of a small number of robust networks which have a rich spatial structure. Yet the temporal information within fMRI data is limited, motivating the complementary analysis of electrophysiological recordings such as electroencephalography (EEG). Here we provide a novel method based on multivariate time-frequency interdependence to reconstruct the principal resting-state network dynamics in human EEG data. The stability of network expression across subjects is assessed using resampling techniques. We report the presence of seven robust networks, with distinct topographic organizations and high frequency (∼ 5-45 Hz) fingerprints, nested within slow temporal sequences that build up and decay over several orders of magnitude. Interestingly, all seven networks are expressed concurrently during these slow dynamics, although there is a temporal asymmetry in the pattern of their formation and dissolution. These analyses uncover the complex temporal character of endogenous cortical fluctuations and, in particular, offer an opportunity to reconstruct the low dimensional linear subspace in which they unfold.

Recent research suggests that neural oscillations in di↵erent frequency bands support distinct and sometimes parallel processing streams in neural circuits. Studies of the neural dynamics of human motor control have primarily focused on oscillations in the beta band (15 30 Hz). During sustained muscle contractions, corticomuscular coherence is mainly present in the beta band, while coherence in the alpha (8 12 Hz) and gamma (30 80 Hz) bands has not been consistently found. Here we test the hypothesis that the frequency of corticomuscular coherence changes during transitions between sensorimotor states. Corticomuscular coherence was investigated in twelve participants making rapid transitions in force output between two targets. Corticomuscular coherence was present in the beta band during sustained contractions but vanished before movement onset, being replaced by transient synchronization in the alpha and gamma bands during dynamic force output. Analysis of the phase spectra suggested a time delay from muscle to cortex for alpha-band coherence, by contrast to a time delay from cortex to muscle for gamma-band coherence, indicating a↵erent and e↵erent corticospinal interactions respectively. Moreover, alpha and gamma -band coherence revealed distinct spatial topologies, suggesting di↵erent generative mechanisms. Coherence in the alpha and gamma bands was almost exclusively confined to trials showing a movement overshoot, suggesting a functional role related to error correction. We interpret the dual-band synchronization in the alpha and gamma bands as parallel streams of corticospinal processing involved in parsing prediction errors and generating new motor predictions.

Interactions between the cerebellum and primary motor cortex are crucial for the acquisition of new motor skills. Recent neuroimaging studies indicate that learning motor skills is associated with subsequent modulation of resting-state functional connectivity in the cerebellar and cerebral cortices. The neuronal processes underlying the motor-learning induced plasticity are not well understood. Here, we investigate changes in functional connectivity in source-reconstructed electroencephalography (EEG) following the performance of a single session of a dynamic force task in twenty young adults. Source activity was reconstructed in 112 regions of interest (ROIs) and the functional connectivity between all ROIs was estimated using imaginary part of the coherence. Significant changes in resting-state connectivity were assessed using partial least squares (PLS). We found that subjects adapted their motor performance during the training session and showed improved accuracy but with slower movement times. A number of connections were significantly upregulated after motor training, principally involving connections within the cerebellum and between the cerebellum and motor cortex. Increased connectivity was confined to specific frequency ranges in the mu and beta bands. Post-hoc analysis of the phase spectra of these cerebellar and corticocerebellar connections revealed an increased phase-lag between motor cortical and cerebellar activity following motor practice. These findings show a reorganization of intrinsic corticocerebellar connectivity related to motor adaption and demonstrate the potential of EEG connectivity analysis in source-space to reveal the neuronal processes that underpin neural plasticity.