Rapid ocular responses are modulated by bottom-up-driven auditory salience

Despite the prevalent use of alerting sounds in alarms and human–machine interface systems and the long-hypothesized role of the auditory system as the brain's “early warning system,” we have only a rudimentary understanding of what determines auditory salience—the automatic attraction of atten...

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Main Authors: Zhao, S, Yum, NW, Benjamin, L, Benhamou, E, Yoneya, M, Furukawa, S, Dick, F, Slaney, M, Chait, M
Format: Journal article
Language:English
Published: Society for Neuroscience 2019
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author Zhao, S
Yum, NW
Benjamin, L
Benhamou, E
Yoneya, M
Furukawa, S
Dick, F
Slaney, M
Chait, M
author_facet Zhao, S
Yum, NW
Benjamin, L
Benhamou, E
Yoneya, M
Furukawa, S
Dick, F
Slaney, M
Chait, M
author_sort Zhao, S
collection OXFORD
description Despite the prevalent use of alerting sounds in alarms and human–machine interface systems and the long-hypothesized role of the auditory system as the brain's “early warning system,” we have only a rudimentary understanding of what determines auditory salience—the automatic attraction of attention by sound—and which brain mechanisms underlie this process. A major roadblock has been the lack of a robust, objective means of quantifying sound-driven attentional capture. Here we demonstrate that: (1) a reliable salience scale can be obtained from crowd-sourcing (N = 911), (2) acoustic roughness appears to be a driving feature behind this scaling, consistent with previous reports implicating roughness in the perceptual distinctiveness of sounds, and (3) crowd-sourced auditory salience correlates with objective autonomic measures. Specifically, we show that a salience ranking obtained from online raters correlated robustly with the superior colliculus-mediated ocular freezing response, microsaccadic inhibition (MSI), measured in naive, passively listening human participants (of either sex). More salient sounds evoked earlier and larger MSI, consistent with a faster orienting response. These results are consistent with the hypothesis that MSI reflects a general reorienting response that is evoked by potentially behaviorally important events regardless of their modality. <br></br> SIGNIFICANCE STATEMENT Microsaccades are small, rapid, fixational eye movements that are measurable with sensitive eye-tracking equipment. We reveal a novel, robust link between microsaccade dynamics and the subjective salience of brief sounds (salience rankings obtained from a large number of participants in an online experiment): Within 300 ms of sound onset, the eyes of naive, passively listening participants demonstrate different microsaccade patterns as a function of the sound's crowd-sourced salience. These results position the superior colliculus (hypothesized to underlie microsaccade generation) as an important brain area to investigate in the context of a putative multimodal salience hub. They also demonstrate an objective means for quantifying auditory salience.
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spelling oxford-uuid:27d5f74f-29ab-4079-95e8-ae1e203cd94d2022-03-26T12:09:13ZRapid ocular responses are modulated by bottom-up-driven auditory salienceJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:27d5f74f-29ab-4079-95e8-ae1e203cd94dEnglishSymplectic ElementsSociety for Neuroscience2019Zhao, SYum, NWBenjamin, LBenhamou, EYoneya, MFurukawa, SDick, FSlaney, MChait, MDespite the prevalent use of alerting sounds in alarms and human–machine interface systems and the long-hypothesized role of the auditory system as the brain's “early warning system,” we have only a rudimentary understanding of what determines auditory salience—the automatic attraction of attention by sound—and which brain mechanisms underlie this process. A major roadblock has been the lack of a robust, objective means of quantifying sound-driven attentional capture. Here we demonstrate that: (1) a reliable salience scale can be obtained from crowd-sourcing (N = 911), (2) acoustic roughness appears to be a driving feature behind this scaling, consistent with previous reports implicating roughness in the perceptual distinctiveness of sounds, and (3) crowd-sourced auditory salience correlates with objective autonomic measures. Specifically, we show that a salience ranking obtained from online raters correlated robustly with the superior colliculus-mediated ocular freezing response, microsaccadic inhibition (MSI), measured in naive, passively listening human participants (of either sex). More salient sounds evoked earlier and larger MSI, consistent with a faster orienting response. These results are consistent with the hypothesis that MSI reflects a general reorienting response that is evoked by potentially behaviorally important events regardless of their modality. <br></br> SIGNIFICANCE STATEMENT Microsaccades are small, rapid, fixational eye movements that are measurable with sensitive eye-tracking equipment. We reveal a novel, robust link between microsaccade dynamics and the subjective salience of brief sounds (salience rankings obtained from a large number of participants in an online experiment): Within 300 ms of sound onset, the eyes of naive, passively listening participants demonstrate different microsaccade patterns as a function of the sound's crowd-sourced salience. These results position the superior colliculus (hypothesized to underlie microsaccade generation) as an important brain area to investigate in the context of a putative multimodal salience hub. They also demonstrate an objective means for quantifying auditory salience.
spellingShingle Zhao, S
Yum, NW
Benjamin, L
Benhamou, E
Yoneya, M
Furukawa, S
Dick, F
Slaney, M
Chait, M
Rapid ocular responses are modulated by bottom-up-driven auditory salience
title Rapid ocular responses are modulated by bottom-up-driven auditory salience
title_full Rapid ocular responses are modulated by bottom-up-driven auditory salience
title_fullStr Rapid ocular responses are modulated by bottom-up-driven auditory salience
title_full_unstemmed Rapid ocular responses are modulated by bottom-up-driven auditory salience
title_short Rapid ocular responses are modulated by bottom-up-driven auditory salience
title_sort rapid ocular responses are modulated by bottom up driven auditory salience
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