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Detailed characterization of neural selectivity in free viewing primates

Fixation constraints in visual tasks are ubiquitous in visual and cognitive neuroscience. Despite its widespread use, fixation requires trained subjects, is limited by the accuracy of fixational eye movements, and ignores the role of eye movements in shaping visual input. To overcome these limitatio...

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Autores principales: Yates, Jacob L., Coop, Shanna H., Sarch, Gabriel H., Wu, Ruei-Jr, Butts, Daniel A., Rucci, Michele, Mitchell, Jude F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282080/
https://www.ncbi.nlm.nih.gov/pubmed/37339973
http://dx.doi.org/10.1038/s41467-023-38564-9
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author Yates, Jacob L.
Coop, Shanna H.
Sarch, Gabriel H.
Wu, Ruei-Jr
Butts, Daniel A.
Rucci, Michele
Mitchell, Jude F.
author_facet Yates, Jacob L.
Coop, Shanna H.
Sarch, Gabriel H.
Wu, Ruei-Jr
Butts, Daniel A.
Rucci, Michele
Mitchell, Jude F.
author_sort Yates, Jacob L.
collection PubMed
description Fixation constraints in visual tasks are ubiquitous in visual and cognitive neuroscience. Despite its widespread use, fixation requires trained subjects, is limited by the accuracy of fixational eye movements, and ignores the role of eye movements in shaping visual input. To overcome these limitations, we developed a suite of hardware and software tools to study vision during natural behavior in untrained subjects. We measured visual receptive fields and tuning properties from multiple cortical areas of marmoset monkeys who freely viewed full-field noise stimuli. The resulting receptive fields and tuning curves from primary visual cortex (V1) and area MT match reported selectivity from the literature which was measured using conventional approaches. We then combined free viewing with high-resolution eye tracking to make the first detailed 2D spatiotemporal measurements of foveal receptive fields in V1. These findings demonstrate the power of free viewing to characterize neural responses in untrained animals while simultaneously studying the dynamics of natural behavior.
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spelling pubmed-102820802023-06-22 Detailed characterization of neural selectivity in free viewing primates Yates, Jacob L. Coop, Shanna H. Sarch, Gabriel H. Wu, Ruei-Jr Butts, Daniel A. Rucci, Michele Mitchell, Jude F. Nat Commun Article Fixation constraints in visual tasks are ubiquitous in visual and cognitive neuroscience. Despite its widespread use, fixation requires trained subjects, is limited by the accuracy of fixational eye movements, and ignores the role of eye movements in shaping visual input. To overcome these limitations, we developed a suite of hardware and software tools to study vision during natural behavior in untrained subjects. We measured visual receptive fields and tuning properties from multiple cortical areas of marmoset monkeys who freely viewed full-field noise stimuli. The resulting receptive fields and tuning curves from primary visual cortex (V1) and area MT match reported selectivity from the literature which was measured using conventional approaches. We then combined free viewing with high-resolution eye tracking to make the first detailed 2D spatiotemporal measurements of foveal receptive fields in V1. These findings demonstrate the power of free viewing to characterize neural responses in untrained animals while simultaneously studying the dynamics of natural behavior. Nature Publishing Group UK 2023-06-20 /pmc/articles/PMC10282080/ /pubmed/37339973 http://dx.doi.org/10.1038/s41467-023-38564-9 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 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
Yates, Jacob L.
Coop, Shanna H.
Sarch, Gabriel H.
Wu, Ruei-Jr
Butts, Daniel A.
Rucci, Michele
Mitchell, Jude F.
Detailed characterization of neural selectivity in free viewing primates
title Detailed characterization of neural selectivity in free viewing primates
title_full Detailed characterization of neural selectivity in free viewing primates
title_fullStr Detailed characterization of neural selectivity in free viewing primates
title_full_unstemmed Detailed characterization of neural selectivity in free viewing primates
title_short Detailed characterization of neural selectivity in free viewing primates
title_sort detailed characterization of neural selectivity in free viewing primates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282080/
https://www.ncbi.nlm.nih.gov/pubmed/37339973
http://dx.doi.org/10.1038/s41467-023-38564-9
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