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Peripheral targets attenuate miniature eye movements during fixation
Fixating a small dot is a universal technique for stabilizing gaze in vision and eye movement research, and for clinical imaging of normal and diseased retinae. During fixation, microsaccades and drifts occur that presumably benefit vision, yet microsaccades compromise image stability and usurp task...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164736/ https://www.ncbi.nlm.nih.gov/pubmed/37150766 http://dx.doi.org/10.1038/s41598-023-34066-2 |
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author | Watamaniuk, Scott N. J. Badler, Jeremy B. Heinen, Stephen J. |
author_facet | Watamaniuk, Scott N. J. Badler, Jeremy B. Heinen, Stephen J. |
author_sort | Watamaniuk, Scott N. J. |
collection | PubMed |
description | Fixating a small dot is a universal technique for stabilizing gaze in vision and eye movement research, and for clinical imaging of normal and diseased retinae. During fixation, microsaccades and drifts occur that presumably benefit vision, yet microsaccades compromise image stability and usurp task attention. Previous work suggested that microsaccades and smooth pursuit catch-up saccades are controlled by similar mechanisms. This, and other previous work showing fewer catch-up saccades during smooth pursuit of peripheral targets suggested that a peripheral target might similarly mitigate microsaccades. Here, human observers fixated one of three stimuli: a small central dot, the center of a peripheral, circular array of small dots, or a central/peripheral stimulus created by combining the two. The microsaccade rate was significantly lower with the peripheral array than with the dot. However, inserting the dot into the array increased the microsaccade rate to single-dot levels. Drift speed also decreased with the peripheral array, both with and without the central dot. Eye position variability was higher with the array than with the composite stimulus. The results suggest that analogous to the foveal pursuit, foveating a stationary target engages the saccadic system likely compromising retinal-image stability. In contrast, fixating a peripheral stimulus improves stability, thereby affording better retinal imaging and releasing attention for experimental tasks. |
format | Online Article Text |
id | pubmed-10164736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101647362023-05-09 Peripheral targets attenuate miniature eye movements during fixation Watamaniuk, Scott N. J. Badler, Jeremy B. Heinen, Stephen J. Sci Rep Article Fixating a small dot is a universal technique for stabilizing gaze in vision and eye movement research, and for clinical imaging of normal and diseased retinae. During fixation, microsaccades and drifts occur that presumably benefit vision, yet microsaccades compromise image stability and usurp task attention. Previous work suggested that microsaccades and smooth pursuit catch-up saccades are controlled by similar mechanisms. This, and other previous work showing fewer catch-up saccades during smooth pursuit of peripheral targets suggested that a peripheral target might similarly mitigate microsaccades. Here, human observers fixated one of three stimuli: a small central dot, the center of a peripheral, circular array of small dots, or a central/peripheral stimulus created by combining the two. The microsaccade rate was significantly lower with the peripheral array than with the dot. However, inserting the dot into the array increased the microsaccade rate to single-dot levels. Drift speed also decreased with the peripheral array, both with and without the central dot. Eye position variability was higher with the array than with the composite stimulus. The results suggest that analogous to the foveal pursuit, foveating a stationary target engages the saccadic system likely compromising retinal-image stability. In contrast, fixating a peripheral stimulus improves stability, thereby affording better retinal imaging and releasing attention for experimental tasks. Nature Publishing Group UK 2023-05-07 /pmc/articles/PMC10164736/ /pubmed/37150766 http://dx.doi.org/10.1038/s41598-023-34066-2 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Watamaniuk, Scott N. J. Badler, Jeremy B. Heinen, Stephen J. Peripheral targets attenuate miniature eye movements during fixation |
title | Peripheral targets attenuate miniature eye movements during fixation |
title_full | Peripheral targets attenuate miniature eye movements during fixation |
title_fullStr | Peripheral targets attenuate miniature eye movements during fixation |
title_full_unstemmed | Peripheral targets attenuate miniature eye movements during fixation |
title_short | Peripheral targets attenuate miniature eye movements during fixation |
title_sort | peripheral targets attenuate miniature eye movements during fixation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164736/ https://www.ncbi.nlm.nih.gov/pubmed/37150766 http://dx.doi.org/10.1038/s41598-023-34066-2 |
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