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A comparative analysis of response times shows that multisensory benefits and interactions are not equivalent
Multisensory signals allow faster responses than the unisensory components. While this redundant signals effect (RSE) has been studied widely with diverse signals, no modelling approach explored the RSE systematically across studies. For a comparative analysis, here, we propose three steps: The firs...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393672/ https://www.ncbi.nlm.nih.gov/pubmed/30814642 http://dx.doi.org/10.1038/s41598-019-39924-6 |
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author | Innes, Bobby R. Otto, Thomas U. |
author_facet | Innes, Bobby R. Otto, Thomas U. |
author_sort | Innes, Bobby R. |
collection | PubMed |
description | Multisensory signals allow faster responses than the unisensory components. While this redundant signals effect (RSE) has been studied widely with diverse signals, no modelling approach explored the RSE systematically across studies. For a comparative analysis, here, we propose three steps: The first quantifies the RSE compared to a simple, parameter-free race model. The second quantifies processing interactions beyond the race mechanism: history effects and so-called violations of Miller’s bound. The third models the RSE on the level of response time distributions using a context-variant race model with two free parameters that account for the interactions. Mimicking the diversity of studies, we tested different audio-visual signals that target the interactions using a 2 × 2 design. We show that the simple race model provides overall a strong prediction of the RSE. Regarding interactions, we found that history effects do not depend on low-level feature repetition. Furthermore, violations of Miller’s bound seem linked to transient signal onsets. Critically, the latter dissociates from the RSE, demonstrating that multisensory interactions and multisensory benefits are not equivalent. Overall, we argue that our approach, as a blueprint, provides both a general framework and the precision needed to understand the RSE when studied across diverse signals and participant groups. |
format | Online Article Text |
id | pubmed-6393672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63936722019-03-04 A comparative analysis of response times shows that multisensory benefits and interactions are not equivalent Innes, Bobby R. Otto, Thomas U. Sci Rep Article Multisensory signals allow faster responses than the unisensory components. While this redundant signals effect (RSE) has been studied widely with diverse signals, no modelling approach explored the RSE systematically across studies. For a comparative analysis, here, we propose three steps: The first quantifies the RSE compared to a simple, parameter-free race model. The second quantifies processing interactions beyond the race mechanism: history effects and so-called violations of Miller’s bound. The third models the RSE on the level of response time distributions using a context-variant race model with two free parameters that account for the interactions. Mimicking the diversity of studies, we tested different audio-visual signals that target the interactions using a 2 × 2 design. We show that the simple race model provides overall a strong prediction of the RSE. Regarding interactions, we found that history effects do not depend on low-level feature repetition. Furthermore, violations of Miller’s bound seem linked to transient signal onsets. Critically, the latter dissociates from the RSE, demonstrating that multisensory interactions and multisensory benefits are not equivalent. Overall, we argue that our approach, as a blueprint, provides both a general framework and the precision needed to understand the RSE when studied across diverse signals and participant groups. Nature Publishing Group UK 2019-02-27 /pmc/articles/PMC6393672/ /pubmed/30814642 http://dx.doi.org/10.1038/s41598-019-39924-6 Text en © The Author(s) 2019 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 Innes, Bobby R. Otto, Thomas U. A comparative analysis of response times shows that multisensory benefits and interactions are not equivalent |
title | A comparative analysis of response times shows that multisensory benefits and interactions are not equivalent |
title_full | A comparative analysis of response times shows that multisensory benefits and interactions are not equivalent |
title_fullStr | A comparative analysis of response times shows that multisensory benefits and interactions are not equivalent |
title_full_unstemmed | A comparative analysis of response times shows that multisensory benefits and interactions are not equivalent |
title_short | A comparative analysis of response times shows that multisensory benefits and interactions are not equivalent |
title_sort | comparative analysis of response times shows that multisensory benefits and interactions are not equivalent |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393672/ https://www.ncbi.nlm.nih.gov/pubmed/30814642 http://dx.doi.org/10.1038/s41598-019-39924-6 |
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