Scale-free fluctuations are ubiquitous in behavioral performance and neuronal activity. In time scales from seconds to hundreds of seconds, psychophysical dynamics and the amplitude fluctuations of neuronal oscillations are governed by power-law-form longrange temporal correlations (LRTCs). In millisecond time scales, neuronal activity comprises cascade-like neuronal avalanches that exhibit power-law size and lifetime distributions. However, it remains unknown whether these neuronal scaling laws are correlated with those characterizing behavioral performance or whether neuronal LRTCs and avalanches are related. Here, we show that the neuronal scaling laws are strongly correlated both with each other and with behavioral scaling laws. We used source reconstructed magneto-and electroencephalographic recordings to characterize the dynamics of ongoing cortical activity. We found robust power-law scaling in neuronal LRTCs and avalanches in resting-state data and during the performance of audiovisual threshold stimulus detection tasks. The LRTC scaling exponents of the behavioral performance fluctuations were correlated with those of concurrent neuronal avalanches and LRTCs in anatomically identified brain systems. The behavioral exponents also were correlated with neuronal scaling laws derived from a resting-state condition and with a similar anatomical topography. Finally, despite the difference in time scales, the scaling exponents of neuronal LRTCs and avalanches were strongly correlated during both rest and task performance. Thus, long and short time-scale neuronal dynamics are related and functionally significant at the behavioral level. These data suggest that the temporal structures of human cognitive fluctuations and behavioral variability stem from the scaling laws of individual and intrinsic brain dynamics.spontaneous activity | threshold detection | criticality H uman cognitive and behavioral performance is highly variable and exhibits slow fluctuations that are salient in continuous performance tasks (CPTs) (1). Psychophysical time series have been known since the early 1950s to be nonrandomly clustered (2), and later studies have shown that hit-rate and/or reaction-time fluctuations in CPT data are fractal and power-law autocorrelated across hundreds of seconds (3-9). The biological origins and relevance of these dynamic, however, remain unclear (10, 11).Similar to those in behavioral performance, the fluctuations of collective neuronal activity at many levels of the nervous system are scale-free and governed by power-law scaling laws. On short time scales (10 −3 −10 −1 s), negative deflections in local field potentials form spatiotemporal cascades of activity, "neuronal avalanches" (32-34), the size and lifetime distributions of which are power laws akin to those of a critical branching process (33). Neuronal avalanches characterize spontaneous neuronal network activity in organotypic cultures (32), brain slices in vitro (35), and monkey (34) and human cortex (36) in vivo. In monkey cortex, the avalanche...