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Single Trial Plasticity in Evidence Accumulation Underlies Rapid Recalibration to Asynchronous Audiovisual Speech
Asynchronous arrival of audiovisual information at the peripheral sensory organs is a ubiquitous property of signals in the natural environment due to differences in the propagation time of light and sound. As these cues are constantly changing their distance from the observer, rapid adaptation to a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104055/ https://www.ncbi.nlm.nih.gov/pubmed/30131578 http://dx.doi.org/10.1038/s41598-018-30414-9 |
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author | Simon, David M. Nidiffer, Aaron R. Wallace, Mark T. |
author_facet | Simon, David M. Nidiffer, Aaron R. Wallace, Mark T. |
author_sort | Simon, David M. |
collection | PubMed |
description | Asynchronous arrival of audiovisual information at the peripheral sensory organs is a ubiquitous property of signals in the natural environment due to differences in the propagation time of light and sound. As these cues are constantly changing their distance from the observer, rapid adaptation to asynchronies is crucial for their appropriate integration. We investigated the neural basis of rapid recalibration to asynchronous audiovisual speech in humans using a combination of psychophysics, drift diffusion modeling, and electroencephalography (EEG). Consistent with previous reports, we found that perception of audiovisual temporal synchrony depends on the temporal ordering of the previous trial. Drift diffusion modelling indicated that this recalibration effect is well accounted for by changes in the rate of evidence accumulation (i.e. drift rate). Neural responses as indexed via evoked potentials were similarly found to vary based on the temporal ordering of the previous trial. Within and across subject correlations indicated that the observed changes in drift rate and the modulation of evoked potential magnitude were related. These results indicate that the rate and direction of evidence accumulation are affected by immediate sensory history and that these changes contribute to single trial recalibration to audiovisual temporal asynchrony. |
format | Online Article Text |
id | pubmed-6104055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61040552018-08-27 Single Trial Plasticity in Evidence Accumulation Underlies Rapid Recalibration to Asynchronous Audiovisual Speech Simon, David M. Nidiffer, Aaron R. Wallace, Mark T. Sci Rep Article Asynchronous arrival of audiovisual information at the peripheral sensory organs is a ubiquitous property of signals in the natural environment due to differences in the propagation time of light and sound. As these cues are constantly changing their distance from the observer, rapid adaptation to asynchronies is crucial for their appropriate integration. We investigated the neural basis of rapid recalibration to asynchronous audiovisual speech in humans using a combination of psychophysics, drift diffusion modeling, and electroencephalography (EEG). Consistent with previous reports, we found that perception of audiovisual temporal synchrony depends on the temporal ordering of the previous trial. Drift diffusion modelling indicated that this recalibration effect is well accounted for by changes in the rate of evidence accumulation (i.e. drift rate). Neural responses as indexed via evoked potentials were similarly found to vary based on the temporal ordering of the previous trial. Within and across subject correlations indicated that the observed changes in drift rate and the modulation of evoked potential magnitude were related. These results indicate that the rate and direction of evidence accumulation are affected by immediate sensory history and that these changes contribute to single trial recalibration to audiovisual temporal asynchrony. Nature Publishing Group UK 2018-08-21 /pmc/articles/PMC6104055/ /pubmed/30131578 http://dx.doi.org/10.1038/s41598-018-30414-9 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Simon, David M. Nidiffer, Aaron R. Wallace, Mark T. Single Trial Plasticity in Evidence Accumulation Underlies Rapid Recalibration to Asynchronous Audiovisual Speech |
title | Single Trial Plasticity in Evidence Accumulation Underlies Rapid Recalibration to Asynchronous Audiovisual Speech |
title_full | Single Trial Plasticity in Evidence Accumulation Underlies Rapid Recalibration to Asynchronous Audiovisual Speech |
title_fullStr | Single Trial Plasticity in Evidence Accumulation Underlies Rapid Recalibration to Asynchronous Audiovisual Speech |
title_full_unstemmed | Single Trial Plasticity in Evidence Accumulation Underlies Rapid Recalibration to Asynchronous Audiovisual Speech |
title_short | Single Trial Plasticity in Evidence Accumulation Underlies Rapid Recalibration to Asynchronous Audiovisual Speech |
title_sort | single trial plasticity in evidence accumulation underlies rapid recalibration to asynchronous audiovisual speech |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104055/ https://www.ncbi.nlm.nih.gov/pubmed/30131578 http://dx.doi.org/10.1038/s41598-018-30414-9 |
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