Very Slow EEG Fluctuations Predict the Dynamics of Stimulus Detection and Oscillation Amplitudes in Humans
Open accessAbstract
Our ability to perceive weak signals is correlated among consecutive trials and fluctuates slowly over time. Although this “streaking effect” has been known for decades, the underlying neural network phenomena have remained largely unidentified. We examined the dynamics of human behavioral performance and its correlation with infraslow (0.01–0.1 Hz) fluctuations in ongoing brain activity. Full-band electroencephalography revealed prominent infraslow fluctuations during the execution of a somatosensory detection task. Similar fluctuations were predominant also in the dynamics of behavioral performance. The subjects' ability to detect the sensory stimuli was strongly correlated with the phase, but not with the amplitude of the infraslow EEG fluctuations. These data thus reveal a direct electrophysiological correlate for the slow fluctuations in human psychophysical performance. We then examined the correlation between the phase of infraslow EEG fluctuations and the amplitude of 1–40 Hz neuronal oscillations in six frequency bands. Like the behavioral performance, the amplitudes in these frequency bands were robustly correlated with the phase of the infraslow fluctuations. These data hence suggest that the infraslow fluctuations reflect the excitability dynamics of cortical networks. We conclude that ongoing 0.01–0.1 Hz EEG fluctuations are prominent and functionally significant during execution of cognitive tasks.
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There is an abundance of evidence that the EEG is organized across multiple time scales, such as in nested oscillations involving both local and global modulations in time.
“In contrast, there is an abundance of evidence that the EEG is organized across multiple time scales, such as in nested oscillations [Canolty et al., 2006; Monto et al., 2008; Schack et al., 2002; Vanhatalo et al., 2004] involving both local and global modulations in time.”
From Deep learning with convolutional neural networks for EEG decoding and visualization (2017) · cites this paper as Monto et al., 2008
Cites
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis
Greicius, M. D., Krasnow, B., Reiss, A. L., & Menon, V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0135058100 · Cited by 6,358 · see citing works
Electrophysiological signatures of resting state networks in the human brain
Mantini, D., Perrucci, M. G., Del Gratta, C., Romani, G. L., & Corbetta, M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700668104 · Cited by 1,938 · see citing works
The neural bases of momentary lapses in attention
Weissman, D. H., Roberts, K. C., Visscher, K. M., & Woldorff, M. G. (2006) · Nature Neuroscience · doi:10.1038/nn1727 · Cited by 1,566 · see citing works
Long-Range Temporal Correlations and Scaling Behavior in Human Brain Oscillations
Linkenkaer-Hansen, K., Nikouline, V. V., Palva, J. M., & Ilmoniemi, R. J. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-04-01370.2001 · Cited by 1,149 · see citing works
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Deep learning with convolutional neural networks for EEG decoding and visualization
Schirrmeister, R. T., Springenberg, J. T., Fiederer, L. D. J., Glasstetter, M., Eggensperger, K., Tangermann, M., Hutter, F., Burgard, W., & Ball, T. (2017) · Human Brain Mapping · doi:10.1002/hbm.23730 · Cited by 3,751 · see citing works
Large-scale brain networks in cognition: emerging methods and principles
Bressler, S. L., & Menon, V. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.04.004 · Cited by 2,348 · see citing works
Emerging concepts for the dynamical organization of resting-state activity in the brain
Deco, G., Jirsa, V. K., & McIntosh, A. R. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn2961 · Cited by 1,798 · see citing works
Low-frequency neuronal oscillations as instruments of sensory selection
Schroeder, C. E., & Lakatos, P. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2008.09.012 · Cited by 1,528 · see citing works
Closed-loop brain training: the science of neurofeedback
Sitaram, R., Ros, T., Stoeckel, L., Haller, S., Scharnowski, F., Lewis-Peacock, J., Weiskopf, N., Blefari, M. L., Rana, M., Oblak, E., et al. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.164 · Cited by 1,306 · see citing works
Raichle, M. E. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.01.008 · Cited by 1,111 · see citing works
The Temporal Structures and Functional Significance of Scale-free Brain Activity
He, B. J., Zempel, J. M., Snyder, A. Z., & Raichle, M. E. (2010) · Neuron · doi:10.1016/j.neuron.2010.04.020 · Cited by 990 · see citing works
Learning sculpts the spontaneous activity of the resting human brain
Lewis, C. M., Baldassarre, A., Committeri, G., Romani, G. L., & Corbetta, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902455106 · Cited by 777 · see citing works
Distilling the neural correlates of consciousness
Aru, J., Bachmann, T., Singer, W., & Melloni, L. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.12.003 · Cited by 589 · see citing works
Intrinsic Coupling Modes: Multiscale Interactions in Ongoing Brain Activity
Engel, A. K., Gerloff, C., Hilgetag, C. C., & Nolte, G. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.038 · Cited by 471 · see citing works
The restless brain: How intrinsic activity organizes brain function
Raichle, M. E. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2014.0172 · Cited by 433 · see citing works
Neuromodulation of brain state and behavior
McCormick, D. A., Nestvogel, D. B., & He, B. J. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-100219-105424 · Cited by 303 · see citing works
Sadaghiani, S., Hesselmann, G., & Kleinschmidt, A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2592-09.2009 · Cited by 325 · see citing works
Mateo, C., Knutsen, P. M., Tsai, P. S., Shih, A. Y., & Kleinfeld, D. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.012 · Cited by 303 · see citing works
Karalunas, S. L., Geurts, H. M., Konrad, K., Bender, S., & Nigg, J. T. (2014) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12217 · Cited by 278 · see citing works
Lecci, S., Fernandez, L. M. J., Weber, F. D., Cardis, R., Chatton, J.-Y., Born, J., & Lüthi, A. (2017) · Science Advances · doi:10.1126/sciadv.1602026 · Cited by 242 · see citing works
Infraslow LFP correlates to resting-state fMRI BOLD signals
Pan, W.-J., Thompson, G. J., Magnuson, M. E., Jaeger, D., & Keilholz, S. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.02.035 · Cited by 231 · see citing works
Spontaneous Infra-slow Brain Activity Has Unique Spatiotemporal Dynamics and Laminar Structure
Mitra, A., Kraft, A., Wright, P., Acland, B., Snyder, A. Z., Rosenthal, Z., Czerniewski, L., Bauer, A., Snyder, L., Culver, J., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.015 · Cited by 193 · see citing works
A place for time: The spatiotemporal structure of neural dynamics during natural audition
Stephens, G. J., Honey, C. J., & Hasson, U. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00268.2013 · Cited by 141 · see citing works
Palva, J. M., & Palva, S. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.060 · Cited by 163 · see citing works
Self-citationWang, L., Saalmann, Y. B., Pinsk, M. A., Arcaro, M. J., & Kastner, S. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.033 · Cited by 158 · see citing works
Infraslow (<0.1Hz) oscillations in thalamic relay nuclei
Hughes, S. W., Lőrincz, M. L., Parri, H. R., & Crunelli, V. (2011) · Progress in Brain Research · doi:10.1016/b978-0-444-53839-0.00010-7 · Cited by 104 · see citing works
ATP-Dependent Infra-Slow (<0.1 Hz) Oscillations in Thalamic Networks
Lőrincz, M. L., Geall, F., Bao, Y., Crunelli, V., & Hughes, S. W. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004447 · Cited by 103 · see citing works
Functional connectivity and neurological recovery
Corbetta, M. (2012) · Developmental Psychobiology · doi:10.1002/dev.20507 · Cited by 96 · see citing works
Quasi-periodic patterns contribute to functional connectivity in the brain
Abbas, A., Belloy, M., Kashyap, A., Billings, J., Nezafati, M., Schumacher, E. H., & Keilholz, S. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.01.076 · Cited by 81 · see citing works
Initial-state-dependent, robust, transient neural dynamics encode conscious visual perception
Baria, A. T., Maniscalco, B., & He, B. J. (2017) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1005806 · Cited by 70 · see citing works
Cognitive and Physiologic Impacts of the Infraslow Oscillation
Watson, B. O. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00044 · Cited by 74 · see citing works
Infraslow Electroencephalographic and Dynamic Resting State Network Activity
Grooms, J. K., Thompson, G. J., Pan, W.-J., Billings, J., Schumacher, E. H., Epstein, C. M., & Keilholz, S. D. (2017) · Brain Connectivity · doi:10.1089/brain.2017.0492 · Cited by 74 · see citing works
Palva, J. M., & Palva, S. (2011) · Progress in Brain Research · doi:10.1016/b978-0-444-53839-0.00022-3 · Cited by 63 · see citing works
Self-citationBönstrup, M., Schulz, R., Feldheim, J., Hummel, F. C., & Gerloff, C. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.08.052 · Cited by 56 · see citing works
Herman, P. A., Lundqvist, M., & Lansner, A. (2013) · Brain Research · doi:10.1016/j.brainres.2013.08.002 · Cited by 47 · see citing works
Perspective: causes and functional significance of temporal variations in attention control
Lenartowicz, A., Simpson, G. V., & Cohen, M. S. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00381 · Cited by 38 · see citing works
Infraslow EEG activity modulates cortical excitability in postanoxic encephalopathy
van Putten, M. J. A. M., Tjepkema-Cloostermans, M. C., & Hofmeijer, J. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00714.2014 · Cited by 27 · see citing works
Dynamic coupling of complex brain networks and dual-task behavior
Alavash, M., Thiel, C. M., & Gießing, C. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.01.028 · Cited by 25 · see citing works
Infraslow activity as a potential modulator of corticomotor excitability
de Goede, A. A., & van Putten, M. J. A. M. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00663.2018 · Cited by 24 · see citing works
Spontaneous Infraslow Fluctuations Modulate Hippocampal EPSP-PS Coupling
Dash, M. B., Ajayi, S., Folsom, L., Gold, P. E., & Korol, D. L. (2018) · eneuro · doi:10.1523/eneuro.0403-17.2017 · Cited by 14 · see citing works
- Authors
- Monto, S., Palva, S., Voipio, J., & Palva, J. M.
- Affiliations
- University of Helsinki (FI)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2008-08-13
- Volume
- 28
- Issue
- 33
- Pages
- 8268-8272
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6670577
- OpenAlex
- W2103528520
- Cited by
- 453
- References
- 4
- Citations by year
- 2026: 14 · 2025: 23 · 2024: 26 · 2023: 16 · 2022: 28 · 2021: 29 · 2020: 18 · 2019: 20 · 2018: 24 · 2017: 31 · 2016: 32 · 2015: 28 · 2014: 27 · 2013: 35 · 2012: 28
- FWCI
- 12.79
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Helsingin Yliopisto
- KAUTE-Säätiö
- Academy of Finland
- Ella ja Georg Ehrnroothin Säätiö
- Emil Aaltosen Säätiö
- Jenny ja Antti Wihurin Rahasto
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › EEG and Brain-Computer Interfaces
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neuroscience and Music Perception
- Keywords
- stimulus detection, neural oscillations, EEG phase, ongoing brain activity, psychophysical performance
- MeSH terms
- Adult, Cerebral Cortex, Electric Stimulation, Electroencephalography, Evoked Potentials, Somatosensory, Humans, Male, Predictive Value of Tests, Psychomotor Performance, Reaction Time
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