Functional MRI (fMRI) studies have shown that low-frequency (<0.1 Hz) spontaneous fluctuations of the blood oxygenation level dependent (BOLD) signal during restful wakefulness are coherent within distributed large-scale cortical and subcortical networks (resting state networks, RSNs). The neuronal mechanisms underlying RSNs remain poorly understood. Here, we describe magnetoencephalographic correspondents of two well-characterized RSNs: the dorsal attention and the default mode networks. Seed-based correlation mapping was performed using time-dependent MEG power reconstructed at each voxel within the brain. The topography of RSNs computed on the basis of extended (5 min) epochs was similar to that observed with fMRI but confined to the same hemisphere as the seed region. Analyses taking into account the nonstationarity of MEG activity showed transient formation of more complete RSNs, including nodes in the contralateral hemisphere. Spectral analysis indicated that RSNs manifest in MEG as synchronous modulation of bandlimited power primarily within the theta, alpha, and beta bands-that is, in frequencies slower than those associated with the local electrophysiological correlates of event-related BOLD responses.resting state networks | default mode network | dorsal attention network | functional MRI T he existence of resting state networks (RSNs) is now a wellestablished fMRI phenomenon (1). The basic finding is that in awake, quietly resting humans, spontaneous, slow (<0.1 Hz) fluctuations of the blood oxygen level dependent (BOLD) signal are temporally coherent within widely distributed functional networks closely resembling those evoked by sensory, motor, and cognitive paradigms (2). Interindividual differences in RSN properties may correlate with cognitive abilities both in health (2) and disease (3). Thus, correlated spontaneous neural activity in distributed brain networks represents a fundamental aspect of brain physiology and psychology. Though there is significant evidence linking stimulusevoked BOLD responses, activations and deactivations both (4), and changes in local field potential (LFP) power, especially in the gamma (40-160 Hz) band, data bearing on the electrophysiological correlates of RSNs are scarce. Recent electrocorticography (ECoG) recordings in human subjects have shown a relationship between the topography of a sensory-motor RSN and slow cortical potentials (5). Slow (∼0.1 Hz) fluctuations of the band-limited gamma power have been also reported as an electrophysiological correlate of BOLD signal fluctuations between brain areas within (5, 6) and across hemispheres in both humans (7) and monkeys (8). Though invasive recordings of electrophysiological activity in animals (8) or humans undergoing surgical management of epilepsy (5, 7) provide high spatial and temporal resolution and specificity, they are not ideal for the study of large-scale RSN in healthy volunteers. Not only are these methods invasive, but recordings through grids or electrodes grids typically cover only a small fraction ...

Summary We used magneto-encephalography to study the temporal dynamics of band-limited power correlation at rest within and across six brain networks previously defined by prior fMRI studies. Epochs of transiently high within-network BLP correlation were identified and correlation of BLP time-series across networks was assessed in these epochs. These analyses demonstrate that functional networks are not equivalent with respect to cross-network interactions. The default-mode network and the posterior cingulate cortex, in particular, exhibit the highest degree of transient BLP correlation with other networks especially in the 14–25 Hz (beta band) frequency range. Our results indicate that the previously demonstrated neuroanatomical centrality of the PCC and DMN has a physiological counterpart in the temporal dynamics of network interaction at behaviorally relevant time scales. This interaction involved subsets of nodes from other networks during periods in which their internal correlation was low.

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The Human Connectome Project (HCP) seeks to map the structural and functional connections between network elements in the human brain. Magnetoencephalography (MEG) provides a temporally rich source of information on brain network dynamics and represents one source of functional connectivity data to be provided by the HCP. High quality MEG data will be collected from 50 twin pairs both in the resting state and during performance of motor, working memory and language tasks. These data will be available to the general community. Additionally, using the cortical parcellation scheme common to all imaging modalities, the HCP will provide processing pipelines for calculating connection matrices as a function of time and frequency. Together with structural and functional data generated using magnetic resonance imaging methods, these data represent a unique opportunity to investigate brain network connectivity in a large cohort of normal adult human subjects. The analysis pipeline software and the dynamic connectivity matrices that it generates will all be made freely available to the research community.