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Selective modulation of visual sensitivity during fixation

During periods of steady fixation, we make small-amplitude ocular movements, termed microsaccades, at a rate of 1–2 every second. Early studies provided evidence that visual sensitivity is reduced during microsaccades—akin to the well-established suppression associated with larger saccades. However,...

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Autores principales: Scholes, Chris, McGraw, Paul V., Roach, Neil W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Physiological Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032122/
https://www.ncbi.nlm.nih.gov/pubmed/29488842
http://dx.doi.org/10.1152/jn.00819.2017
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author Scholes, Chris
McGraw, Paul V.
Roach, Neil W.
author_facet Scholes, Chris
McGraw, Paul V.
Roach, Neil W.
author_sort Scholes, Chris
collection PubMed
description During periods of steady fixation, we make small-amplitude ocular movements, termed microsaccades, at a rate of 1–2 every second. Early studies provided evidence that visual sensitivity is reduced during microsaccades—akin to the well-established suppression associated with larger saccades. However, the results of more recent work suggest that microsaccades may alter retinal input in a manner that enhances visual sensitivity to some stimuli. Here we parametrically varied the spatial frequency of a stimulus during a detection task and tracked contrast sensitivity as a function of time relative to microsaccades. Our data reveal two distinct modulations of sensitivity: suppression during the eye movement itself and facilitation after the eye has stopped moving. The magnitude of suppression and facilitation of visual sensitivity is related to the spatial content of the stimulus: suppression is greatest for low spatial frequencies, while sensitivity is enhanced most for stimuli of 1–2 cycles/°, spatial frequencies at which we are already most sensitive in the absence of eye movements. We present a model in which the tuning of suppression and facilitation is explained by delayed lateral inhibition between spatial frequency channels. Our data show that eye movements actively modulate visual sensitivity even during fixation: the detectability of images at different spatial scales can be increased or decreased depending on when the image occurs relative to a microsaccade. NEW & NOTEWORTHY Given the frequency with which we make microsaccades during periods of fixation, it is vital that we understand how they affect visual processing. We demonstrate two selective modulations of contrast sensitivity that are time-locked to the occurrence of a microsaccade: suppression of low spatial frequencies during each eye movement and enhancement of higher spatial frequencies after the eye has stopped moving. These complementary changes may arise naturally because of sluggish gain control between spatial channels.
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spelling pubmed-60321222018-07-06 Selective modulation of visual sensitivity during fixation Scholes, Chris McGraw, Paul V. Roach, Neil W. J Neurophysiol Research Article During periods of steady fixation, we make small-amplitude ocular movements, termed microsaccades, at a rate of 1–2 every second. Early studies provided evidence that visual sensitivity is reduced during microsaccades—akin to the well-established suppression associated with larger saccades. However, the results of more recent work suggest that microsaccades may alter retinal input in a manner that enhances visual sensitivity to some stimuli. Here we parametrically varied the spatial frequency of a stimulus during a detection task and tracked contrast sensitivity as a function of time relative to microsaccades. Our data reveal two distinct modulations of sensitivity: suppression during the eye movement itself and facilitation after the eye has stopped moving. The magnitude of suppression and facilitation of visual sensitivity is related to the spatial content of the stimulus: suppression is greatest for low spatial frequencies, while sensitivity is enhanced most for stimuli of 1–2 cycles/°, spatial frequencies at which we are already most sensitive in the absence of eye movements. We present a model in which the tuning of suppression and facilitation is explained by delayed lateral inhibition between spatial frequency channels. Our data show that eye movements actively modulate visual sensitivity even during fixation: the detectability of images at different spatial scales can be increased or decreased depending on when the image occurs relative to a microsaccade. NEW & NOTEWORTHY Given the frequency with which we make microsaccades during periods of fixation, it is vital that we understand how they affect visual processing. We demonstrate two selective modulations of contrast sensitivity that are time-locked to the occurrence of a microsaccade: suppression of low spatial frequencies during each eye movement and enhancement of higher spatial frequencies after the eye has stopped moving. These complementary changes may arise naturally because of sluggish gain control between spatial channels. American Physiological Society 2018-06-01 2018-02-28 /pmc/articles/PMC6032122/ /pubmed/29488842 http://dx.doi.org/10.1152/jn.00819.2017 Text en Copyright © 2018 the American Physiological Society http://creativecommons.org/licenses/by/4.0/deed.en_US Licensed under Creative Commons Attribution CC-BY 4.0 (http://creativecommons.org/licenses/by/4.0/deed.en_US) : © the American Physiological Society.
spellingShingle Research Article
Scholes, Chris
McGraw, Paul V.
Roach, Neil W.
Selective modulation of visual sensitivity during fixation
title Selective modulation of visual sensitivity during fixation
title_full Selective modulation of visual sensitivity during fixation
title_fullStr Selective modulation of visual sensitivity during fixation
title_full_unstemmed Selective modulation of visual sensitivity during fixation
title_short Selective modulation of visual sensitivity during fixation
title_sort selective modulation of visual sensitivity during fixation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032122/
https://www.ncbi.nlm.nih.gov/pubmed/29488842
http://dx.doi.org/10.1152/jn.00819.2017
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