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A linear oscillator model predicts dynamic temporal attention and pupillary entrainment to rhythmic patterns
Rhythm is a ubiquitous feature of music that induces specific neural modes of processing. In this paper, we assess the potential of a stimulus-driven linear oscillator model (57) to predict dynamic attention to complex musical rhythms on an instant-by-instant basis. We use perceptual thresholds and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bern Open Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898576/ https://www.ncbi.nlm.nih.gov/pubmed/33828695 http://dx.doi.org/10.16910/jemr.11.2.12 |
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author | Fink, Lauren K. Hurley, Brian K. Geng, Joy J. Janata, Petr |
author_facet | Fink, Lauren K. Hurley, Brian K. Geng, Joy J. Janata, Petr |
author_sort | Fink, Lauren K. |
collection | PubMed |
description | Rhythm is a ubiquitous feature of music that induces specific neural modes of processing. In this paper, we assess the potential of a stimulus-driven linear oscillator model (57) to predict dynamic attention to complex musical rhythms on an instant-by-instant basis. We use perceptual thresholds and pupillometry as attentional indices against which to test our model predictions. During a deviance detection task, participants listened to continuously looping, multiinstrument, rhythmic patterns, while being eye-tracked. Their task was to respond anytime they heard an increase in intensity (dB SPL). An adaptive thresholding algorithm adjusted deviant intensity at multiple probed temporal locations throughout each rhythmic stimulus. The oscillator model predicted participants’ perceptual thresholds for detecting deviants at probed locations, with a low temporal salience prediction corresponding to a high perceptual threshold and vice versa. A pupil dilation response was observed for all deviants. Notably, the pupil dilated even when participants did not report hearing a deviant. Maximum pupil size and resonator model output were significant predictors of whether a deviant was detected or missed on any given trial. Besides the evoked pupillary response to deviants, we also assessed the continuous pupillary signal to the rhythmic patterns. The pupil exhibited entrainment at prominent periodicities present in the stimuli and followed each of the different rhythmic patterns in a unique way. Overall, these results replicate previous studies using the linear oscillator model to predict dynamic attention to complex auditory scenes and extend the utility of the model to the prediction of neurophysiological signals, in this case the pupillary time course; however, we note that the amplitude envelope of the acoustic patterns may serve as a similarly useful predictor. To our knowledge, this is the first paper to show entrainment of pupil dynamics by demonstrating a phase relationship between musical stimuli and the pupillary signal. |
format | Online Article Text |
id | pubmed-7898576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Bern Open Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-78985762021-04-06 A linear oscillator model predicts dynamic temporal attention and pupillary entrainment to rhythmic patterns Fink, Lauren K. Hurley, Brian K. Geng, Joy J. Janata, Petr J Eye Mov Res Research Article Rhythm is a ubiquitous feature of music that induces specific neural modes of processing. In this paper, we assess the potential of a stimulus-driven linear oscillator model (57) to predict dynamic attention to complex musical rhythms on an instant-by-instant basis. We use perceptual thresholds and pupillometry as attentional indices against which to test our model predictions. During a deviance detection task, participants listened to continuously looping, multiinstrument, rhythmic patterns, while being eye-tracked. Their task was to respond anytime they heard an increase in intensity (dB SPL). An adaptive thresholding algorithm adjusted deviant intensity at multiple probed temporal locations throughout each rhythmic stimulus. The oscillator model predicted participants’ perceptual thresholds for detecting deviants at probed locations, with a low temporal salience prediction corresponding to a high perceptual threshold and vice versa. A pupil dilation response was observed for all deviants. Notably, the pupil dilated even when participants did not report hearing a deviant. Maximum pupil size and resonator model output were significant predictors of whether a deviant was detected or missed on any given trial. Besides the evoked pupillary response to deviants, we also assessed the continuous pupillary signal to the rhythmic patterns. The pupil exhibited entrainment at prominent periodicities present in the stimuli and followed each of the different rhythmic patterns in a unique way. Overall, these results replicate previous studies using the linear oscillator model to predict dynamic attention to complex auditory scenes and extend the utility of the model to the prediction of neurophysiological signals, in this case the pupillary time course; however, we note that the amplitude envelope of the acoustic patterns may serve as a similarly useful predictor. To our knowledge, this is the first paper to show entrainment of pupil dynamics by demonstrating a phase relationship between musical stimuli and the pupillary signal. Bern Open Publishing 2018-11-20 /pmc/articles/PMC7898576/ /pubmed/33828695 http://dx.doi.org/10.16910/jemr.11.2.12 Text en This work is licensed under a Creative Commons Attribution 4.0 International License, ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Article Fink, Lauren K. Hurley, Brian K. Geng, Joy J. Janata, Petr A linear oscillator model predicts dynamic temporal attention and pupillary entrainment to rhythmic patterns |
title | A linear oscillator model predicts
dynamic temporal attention and
pupillary entrainment to rhythmic patterns |
title_full | A linear oscillator model predicts
dynamic temporal attention and
pupillary entrainment to rhythmic patterns |
title_fullStr | A linear oscillator model predicts
dynamic temporal attention and
pupillary entrainment to rhythmic patterns |
title_full_unstemmed | A linear oscillator model predicts
dynamic temporal attention and
pupillary entrainment to rhythmic patterns |
title_short | A linear oscillator model predicts
dynamic temporal attention and
pupillary entrainment to rhythmic patterns |
title_sort | linear oscillator model predicts
dynamic temporal attention and
pupillary entrainment to rhythmic patterns |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898576/ https://www.ncbi.nlm.nih.gov/pubmed/33828695 http://dx.doi.org/10.16910/jemr.11.2.12 |
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