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Temporal dynamics of saccades explained by a self-paced process
Sensory organs are thought to sample the environment rhythmically thereby providing periodic perceptual input. Whisking and sniffing are governed by oscillators which impose rhythms on the motor-control of sensory acquisition and consequently on sensory input. Saccadic eye movements are the main vis...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430543/ https://www.ncbi.nlm.nih.gov/pubmed/28428540 http://dx.doi.org/10.1038/s41598-017-00881-7 |
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author | Amit, Roy Abeles, Dekel Bar-Gad, Izhar Yuval-Greenberg, Shlomit |
author_facet | Amit, Roy Abeles, Dekel Bar-Gad, Izhar Yuval-Greenberg, Shlomit |
author_sort | Amit, Roy |
collection | PubMed |
description | Sensory organs are thought to sample the environment rhythmically thereby providing periodic perceptual input. Whisking and sniffing are governed by oscillators which impose rhythms on the motor-control of sensory acquisition and consequently on sensory input. Saccadic eye movements are the main visual sampling mechanism in primates, and were suggested to constitute part of such a rhythmic exploration system. In this study we characterized saccadic rhythmicity, and examined whether it is consistent with autonomous oscillatory generator or with self-paced generation. Eye movements were tracked while observers were either free-viewing a movie or fixating a static stimulus. We inspected the temporal dynamics of exploratory and fixational saccades and quantified their first-order and high-order dependencies. Data were analyzed using methods derived from spike-train analysis, and tested against mathematical models and simulations. The findings show that saccade timings are explained by first-order dependencies, specifically by their refractory period. Saccade-timings are inconsistent with an autonomous pace-maker but are consistent with a “self-paced” generator, where each saccade is a link in a chain of neural processes that depend on the outcome of the saccade itself. We propose a mathematical model parsimoniously capturing various facets of saccade-timings, and suggest a possible neural mechanism producing the observed dynamics. |
format | Online Article Text |
id | pubmed-5430543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54305432017-05-15 Temporal dynamics of saccades explained by a self-paced process Amit, Roy Abeles, Dekel Bar-Gad, Izhar Yuval-Greenberg, Shlomit Sci Rep Article Sensory organs are thought to sample the environment rhythmically thereby providing periodic perceptual input. Whisking and sniffing are governed by oscillators which impose rhythms on the motor-control of sensory acquisition and consequently on sensory input. Saccadic eye movements are the main visual sampling mechanism in primates, and were suggested to constitute part of such a rhythmic exploration system. In this study we characterized saccadic rhythmicity, and examined whether it is consistent with autonomous oscillatory generator or with self-paced generation. Eye movements were tracked while observers were either free-viewing a movie or fixating a static stimulus. We inspected the temporal dynamics of exploratory and fixational saccades and quantified their first-order and high-order dependencies. Data were analyzed using methods derived from spike-train analysis, and tested against mathematical models and simulations. The findings show that saccade timings are explained by first-order dependencies, specifically by their refractory period. Saccade-timings are inconsistent with an autonomous pace-maker but are consistent with a “self-paced” generator, where each saccade is a link in a chain of neural processes that depend on the outcome of the saccade itself. We propose a mathematical model parsimoniously capturing various facets of saccade-timings, and suggest a possible neural mechanism producing the observed dynamics. Nature Publishing Group UK 2017-04-20 /pmc/articles/PMC5430543/ /pubmed/28428540 http://dx.doi.org/10.1038/s41598-017-00881-7 Text en © The Author(s) 2017 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 Amit, Roy Abeles, Dekel Bar-Gad, Izhar Yuval-Greenberg, Shlomit Temporal dynamics of saccades explained by a self-paced process |
title | Temporal dynamics of saccades explained by a self-paced process |
title_full | Temporal dynamics of saccades explained by a self-paced process |
title_fullStr | Temporal dynamics of saccades explained by a self-paced process |
title_full_unstemmed | Temporal dynamics of saccades explained by a self-paced process |
title_short | Temporal dynamics of saccades explained by a self-paced process |
title_sort | temporal dynamics of saccades explained by a self-paced process |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430543/ https://www.ncbi.nlm.nih.gov/pubmed/28428540 http://dx.doi.org/10.1038/s41598-017-00881-7 |
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