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Neural integration underlying naturalistic prediction flexibly adapts to varying sensory input rate
Prediction of future sensory input based on past sensory information is essential for organisms to effectively adapt their behavior in dynamic environments. Humans successfully predict future stimuli in various natural settings. Yet, it remains elusive how the brain achieves effective prediction des...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113607/ https://www.ncbi.nlm.nih.gov/pubmed/33976118 http://dx.doi.org/10.1038/s41467-021-22632-z |
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author | Baumgarten, Thomas J. Maniscalco, Brian Lee, Jennifer L. Flounders, Matthew W. Abry, Patrice He, Biyu J. |
author_facet | Baumgarten, Thomas J. Maniscalco, Brian Lee, Jennifer L. Flounders, Matthew W. Abry, Patrice He, Biyu J. |
author_sort | Baumgarten, Thomas J. |
collection | PubMed |
description | Prediction of future sensory input based on past sensory information is essential for organisms to effectively adapt their behavior in dynamic environments. Humans successfully predict future stimuli in various natural settings. Yet, it remains elusive how the brain achieves effective prediction despite enormous variations in sensory input rate, which directly affect how fast sensory information can accumulate. We presented participants with acoustic sequences capturing temporal statistical regularities prevalent in nature and investigated neural mechanisms underlying predictive computation using MEG. By parametrically manipulating sequence presentation speed, we tested two hypotheses: neural prediction relies on integrating past sensory information over fixed time periods or fixed amounts of information. We demonstrate that across halved and doubled presentation speeds, predictive information in neural activity stems from integration over fixed amounts of information. Our findings reveal the neural mechanisms enabling humans to robustly predict dynamic stimuli in natural environments despite large sensory input rate variations. |
format | Online Article Text |
id | pubmed-8113607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81136072021-05-14 Neural integration underlying naturalistic prediction flexibly adapts to varying sensory input rate Baumgarten, Thomas J. Maniscalco, Brian Lee, Jennifer L. Flounders, Matthew W. Abry, Patrice He, Biyu J. Nat Commun Article Prediction of future sensory input based on past sensory information is essential for organisms to effectively adapt their behavior in dynamic environments. Humans successfully predict future stimuli in various natural settings. Yet, it remains elusive how the brain achieves effective prediction despite enormous variations in sensory input rate, which directly affect how fast sensory information can accumulate. We presented participants with acoustic sequences capturing temporal statistical regularities prevalent in nature and investigated neural mechanisms underlying predictive computation using MEG. By parametrically manipulating sequence presentation speed, we tested two hypotheses: neural prediction relies on integrating past sensory information over fixed time periods or fixed amounts of information. We demonstrate that across halved and doubled presentation speeds, predictive information in neural activity stems from integration over fixed amounts of information. Our findings reveal the neural mechanisms enabling humans to robustly predict dynamic stimuli in natural environments despite large sensory input rate variations. Nature Publishing Group UK 2021-05-11 /pmc/articles/PMC8113607/ /pubmed/33976118 http://dx.doi.org/10.1038/s41467-021-22632-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Baumgarten, Thomas J. Maniscalco, Brian Lee, Jennifer L. Flounders, Matthew W. Abry, Patrice He, Biyu J. Neural integration underlying naturalistic prediction flexibly adapts to varying sensory input rate |
title | Neural integration underlying naturalistic prediction flexibly adapts to varying sensory input rate |
title_full | Neural integration underlying naturalistic prediction flexibly adapts to varying sensory input rate |
title_fullStr | Neural integration underlying naturalistic prediction flexibly adapts to varying sensory input rate |
title_full_unstemmed | Neural integration underlying naturalistic prediction flexibly adapts to varying sensory input rate |
title_short | Neural integration underlying naturalistic prediction flexibly adapts to varying sensory input rate |
title_sort | neural integration underlying naturalistic prediction flexibly adapts to varying sensory input rate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113607/ https://www.ncbi.nlm.nih.gov/pubmed/33976118 http://dx.doi.org/10.1038/s41467-021-22632-z |
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