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Neural dynamics of phoneme sequences reveal position-invariant code for content and order
Speech consists of a continuously-varying acoustic signal. Yet human listeners experience it as sequences of discrete speech sounds, which are used to recognise discrete words. To examine how the human brain appropriately sequences the speech signal, we recorded two-hour magnetoencephalograms from 2...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633780/ https://www.ncbi.nlm.nih.gov/pubmed/36329058 http://dx.doi.org/10.1038/s41467-022-34326-1 |
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author | Gwilliams, Laura King, Jean-Remi Marantz, Alec Poeppel, David |
author_facet | Gwilliams, Laura King, Jean-Remi Marantz, Alec Poeppel, David |
author_sort | Gwilliams, Laura |
collection | PubMed |
description | Speech consists of a continuously-varying acoustic signal. Yet human listeners experience it as sequences of discrete speech sounds, which are used to recognise discrete words. To examine how the human brain appropriately sequences the speech signal, we recorded two-hour magnetoencephalograms from 21 participants listening to short narratives. Our analyses show that the brain continuously encodes the three most recently heard speech sounds in parallel, and maintains this information long past its dissipation from the sensory input. Each speech sound representation evolves over time, jointly encoding both its phonetic features and the amount of time elapsed since onset. As a result, this dynamic neural pattern encodes both the relative order and phonetic content of the speech sequence. These representations are active earlier when phonemes are more predictable, and are sustained longer when lexical identity is uncertain. Our results show how phonetic sequences in natural speech are represented at the level of populations of neurons, providing insight into what intermediary representations exist between the sensory input and sub-lexical units. The flexibility in the dynamics of these representations paves the way for further understanding of how such sequences may be used to interface with higher order structure such as lexical identity. |
format | Online Article Text |
id | pubmed-9633780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96337802022-11-05 Neural dynamics of phoneme sequences reveal position-invariant code for content and order Gwilliams, Laura King, Jean-Remi Marantz, Alec Poeppel, David Nat Commun Article Speech consists of a continuously-varying acoustic signal. Yet human listeners experience it as sequences of discrete speech sounds, which are used to recognise discrete words. To examine how the human brain appropriately sequences the speech signal, we recorded two-hour magnetoencephalograms from 21 participants listening to short narratives. Our analyses show that the brain continuously encodes the three most recently heard speech sounds in parallel, and maintains this information long past its dissipation from the sensory input. Each speech sound representation evolves over time, jointly encoding both its phonetic features and the amount of time elapsed since onset. As a result, this dynamic neural pattern encodes both the relative order and phonetic content of the speech sequence. These representations are active earlier when phonemes are more predictable, and are sustained longer when lexical identity is uncertain. Our results show how phonetic sequences in natural speech are represented at the level of populations of neurons, providing insight into what intermediary representations exist between the sensory input and sub-lexical units. The flexibility in the dynamics of these representations paves the way for further understanding of how such sequences may be used to interface with higher order structure such as lexical identity. Nature Publishing Group UK 2022-11-03 /pmc/articles/PMC9633780/ /pubmed/36329058 http://dx.doi.org/10.1038/s41467-022-34326-1 Text en © The Author(s) 2022 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 Gwilliams, Laura King, Jean-Remi Marantz, Alec Poeppel, David Neural dynamics of phoneme sequences reveal position-invariant code for content and order |
title | Neural dynamics of phoneme sequences reveal position-invariant code for content and order |
title_full | Neural dynamics of phoneme sequences reveal position-invariant code for content and order |
title_fullStr | Neural dynamics of phoneme sequences reveal position-invariant code for content and order |
title_full_unstemmed | Neural dynamics of phoneme sequences reveal position-invariant code for content and order |
title_short | Neural dynamics of phoneme sequences reveal position-invariant code for content and order |
title_sort | neural dynamics of phoneme sequences reveal position-invariant code for content and order |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633780/ https://www.ncbi.nlm.nih.gov/pubmed/36329058 http://dx.doi.org/10.1038/s41467-022-34326-1 |
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