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Rapid Ocular Responses Are Modulated by Bottom-up-Driven Auditory Salience.
Zhao, Sijia; Yum, Nga Wai; Benjamin, Lucas; Benhamou, Elia; Yoneya, Makoto; Furukawa, Shigeto; Dick, Fred; Slaney, Malcolm; Chait, Maria.
Affiliation
  • Zhao S; Ear Institute, University College London, London WC1X 8EE, United Kingdom, m.chait@ucl.ac.uk sijia.zhao.10@ucl.ac.uk.
  • Yum NW; Ear Institute, University College London, London WC1X 8EE, United Kingdom.
  • Benjamin L; Ear Institute, University College London, London WC1X 8EE, United Kingdom.
  • Benhamou E; Dementia Research Centre, Department of Neurodegenerative Disease, University College London, London WC1N 3AR, United Kingdom.
  • Yoneya M; NTT Communication Science Laboratories, NTT Corporation, Atsugi 243-0198 Japan.
  • Furukawa S; NTT Communication Science Laboratories, NTT Corporation, Atsugi 243-0198 Japan.
  • Dick F; Department of Psychological Sciences, Birkbeck College, London WC1 7HX, United Kingdom.
  • Slaney M; Department of Experimental Psychology, University College London, London WC1H 0DS, United Kingdom, and.
  • Chait M; Machine Hearing Research, Google, Mountain View, California 94043.
J Neurosci ; 39(39): 7703-7714, 2019 09 25.
Article in En | MEDLINE | ID: mdl-31391262
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.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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Saccades / Attention / Auditory Perception / Superior Colliculi Limits: Adolescent / Adult / Female / Humans / Male Language: En Journal: J Neurosci Year: 2019 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Saccades / Attention / Auditory Perception / Superior Colliculi Limits: Adolescent / Adult / Female / Humans / Male Language: En Journal: J Neurosci Year: 2019 Document type: Article Country of publication: United States