ArticleFrontiers in computational neuroscience2016
Statistical Evaluation of Waveform Collapse Reveals Scale-Free Properties of Neuronal Avalanches.
Article in Frontiers in computational neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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8 citing papers in PubMed.
- Neuronal Population Transitions Across a Quiescent-to-Active Frontier and Bifurcation.Frontiers in physiology · 2022Article
- Theoretical foundations of studying criticality in the brain.Network neuroscience (Cambridge, Mass.) · 2022Review
- Toward a Unified Analysis of the Brain Criticality Hypothesis: Reviewing Several Available Tools.Frontiers in neural circuits · 2022Review
- The scale-invariant, temporal profile of neuronal avalanches in relation to cortical γ-oscillations.Scientific reports · 2019Article
- Single-Cell Membrane Potential Fluctuations Evince Network Scale-Freeness and Quasicriticality.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019Article
- Subsampling scaling.Nature communications · 2017Article
- Analysis of Power Laws, Shape Collapses, and Neural Complexity: New Techniques and MATLAB Support via the NCC Toolbox.Frontiers in physiology · 2016Article
- Criticality Maximizes Complexity in Neural Tissue.Frontiers in physiology · 2016Article
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2 authors.
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Abstract
Neural avalanches are a prominent form of brain activity characterized by network-wide bursts whose statistics follow a power-law distribution with a slope near 3/2. Recent work suggests that avalanches of different durations can be rescaled and thus collapsed together. This collapse mirrors work in statistical physics where it is proposed to form a signature of systems evolving in a critical state. However, no rigorous statistical test has been proposed to examine the degree to which neuronal avalanches collapse together. Here, we describe a statistical test based on functional data analysis, where raw avalanches are first smoothed with a Fourier basis, then rescaled using a time-warping function. Finally, an F ratio test combined with a bootstrap permutation is employed to determine if avalanches collapse together in a statistically reliable fashion. To illustrate this approach, we recorded avalanches from cortical cultures on multielectrode arrays as in previous work. Analyses show that avalanches of various durations can be collapsed together in a statistically robust fashion. However, a principal components analysis revealed that the offset of avalanches resulted in marked variance in the time-warping function, thus arguing for limitations to the strict fractal nature of avalanche dynamics. We compared these results with those obtained from cultures treated with an AMPA/NMDA receptor antagonist (APV/DNQX), which yield a power-law of avalanche durations with a slope greater than 3/2. When collapsed together, these avalanches showed marked misalignments both at onset and offset time-points. In sum, the proposed statistical evaluation suggests the presence of scale-free avalanche waveforms and constitutes an avenue for examining critical dynamics in neuronal systems.
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