Literature DB >> 25462792

Duration estimation entails predicting when.

Virginie van Wassenhove1, Lucille Lecoutre2.   

Abstract

The estimation of duration can be affected by context and surprise. Using MagnetoEncephaloGraphy (MEG), we tested whether increased neural activity during surprise and following neural suppression in two different contexts supported subjective time dilation (Eagleman and Pariyadath, 2009; Pariyadath and Eagleman, 2012). Sequences of three 300 ms frequency-modulated (FM, control) or pure tones (test) were presented and followed by a fourth FM varying in duration. In test, the last FM was perceived as significantly longer than veridical duration (Tse et al., 2004) but did not differ from the perceived duration in control. Several novel and distinct neural signatures were observed in duration estimation: first, neural suppression of standard stimuli was observed for the onset but not for the offset auditory evoked responses. Second, ramping activity increased with veridical duration in control whereas at the same latency in test, the amplitude of the midlatency response increased with the distance of deviant durations. Third, in both conditions, the amplitude of the offset auditory evoked responses accounted well for participants' performance: the longer the perceived duration, the larger the offset response. Fourth, neural duration demarcated by the peak latencies of the onset and ramping evoked activities indexed a systematic time compression that reliably predicted subjective time perception. Our findings suggest that interval timing undergoes time compression by capitalizing on the predicted offset of an auditory event.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Interval timing; MMN; Midlatency response; Predictive coding; Ramping activity

Mesh:

Year:  2014        PMID: 25462792     DOI: 10.1016/j.neuroimage.2014.11.005

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


  7 in total

1.  The role of cortical beta oscillations in time estimation.

Authors:  Shrikanth Kulashekhar; Johanna Pekkola; Jaakko Matias Palva; Satu Palva
Journal:  Hum Brain Mapp       Date:  2016-05-11       Impact factor: 5.038

2.  Interval timing in a hierarchical violation-of-expectation task: Dissociable effects of local and global predictions.

Authors:  Shamini Warda; Azizuddin Khan
Journal:  Atten Percept Psychophys       Date:  2022-07-07       Impact factor: 2.157

3.  Spatiotemporal brain dynamics of auditory temporal assimilation.

Authors:  Naruhito Hironaga; Takako Mitsudo; Mariko Hayamizu; Yoshitaka Nakajima; Hiroshige Takeichi; Shozo Tobimatsu
Journal:  Sci Rep       Date:  2017-09-12       Impact factor: 4.379

4.  Diminished neural resources allocation to time processing in Autism Spectrum Disorders.

Authors:  Anna Lambrechts; Christine M Falter-Wagner; Virginie van Wassenhove
Journal:  Neuroimage Clin       Date:  2017-09-28       Impact factor: 4.881

5.  Activity in perceptual classification networks as a basis for human subjective time perception.

Authors:  Warrick Roseboom; Zafeirios Fountas; Kyriacos Nikiforou; David Bhowmik; Murray Shanahan; Anil K Seth
Journal:  Nat Commun       Date:  2019-01-17       Impact factor: 14.919

6.  A generic deviance detection principle for cortical On/Off responses, omission response, and mismatch negativity.

Authors:  Vincent S C Chien; Burkhard Maess; Thomas R Knösche
Journal:  Biol Cybern       Date:  2019-08-19       Impact factor: 2.086

7.  Entire Sound Representations Are Time-Compressed in Sensory Memory: Evidence from MMN.

Authors:  Seiji Tamakoshi; Nanako Minoura; Jun'ichi Katayama; Akihiro Yagi
Journal:  Front Neurosci       Date:  2016-07-26       Impact factor: 4.677

  7 in total

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