Neural correlates of aftereffects induced by adaptations to single and average durations.

duration aftereffect duration perception fMRI long-term adaptation

Journal

PsyCh journal
ISSN: 2046-0260
Titre abrégé: Psych J
Pays: Australia
ID NLM: 101598595

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 05 03 2022
accepted: 13 01 2023
medline: 15 3 2023
pubmed: 15 3 2023
entrez: 14 3 2023
Statut: ppublish

Résumé

Duration perception can be heavily distorted owing to repetitive exposure to a relatively long or short sensory event, often causing a duration aftereffect. Here, we used a novel procedure to show that adaptations to both single and average durations produced the duration aftereffect. Participants completed a duration reproduction task (Experiment 1) or a duration category rating task (Experiment 2) after long-term adaptations to a stimulus of medium duration and to stimuli of averagely medium duration. We found that adaptations to both single and average durations resulted in duration aftereffects. The simultaneously recorded functional magnetic resonance imaging (fMRI) data revealed that the reduction in neural activity due to long-term adaptation to single duration was observed in the right supramarginal gyrus (SMG) of the parietal lobe, while adaptation to average duration resulted in fMRI adaptations in the left postcentral gyrus (PCG) and middle cingulate gyrus (MCG). At the individual level, the magnitude of the behavioral aftereffect was positively correlated with the magnitude of fMRI adaptation in the right SMG after adaptation to single duration, while there were no significantly positive correlations between the behavioral aftereffect and fMRI adaptations in the left PCG and MCG. These results suggest that there are different neural mechanisms for aftereffects caused by adaptations to single and average durations.

Identifiants

pubmed: 36916767
doi: 10.1002/pchj.640
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

479-490

Subventions

Organisme : National Natural Science Foundation of China
ID : 32000744

Informations de copyright

© 2023 Institute of Psychology, Chinese Academy of Sciences and John Wiley & Sons Australia, Ltd.

Références

Alvarez, G. A. (2011). Representing multiple objects as an ensemble enhances visual cognition. Trends in Cognitive Sciences, 15(3), 122-131. https://doi.org/10.1016/j.tics.2011.01.003
Becker, M. W., & Rasmussen, I. P. (2007). The rhythm aftereffect: Support for time sensitive neurons with broad overlapping tuning curves. Brain and Cognition, 64(3), 274-281. https://doi.org/10.1016/j.bandc.2007.03.009
Benton, C. P., & Redfern, A. S. (2016). Perceived duration increases with contrast, but only a little. Frontiers in Psychology, 7, 1950. https://doi.org/10.3389/fpsyg.2016.01950
Bruno, A., Ayhan, I., & Johnston, A. (2011). Duration expansion at low luminance levels. Journal of Vision, 11(14), 1-13. https://doi.org/10.1167/11.14.13
Bruno, A., & Johnston, A. (2010). Contrast gain shapes visual time. Frontiers in Psychology, 1, 170. https://doi.org/10.3389/fpsyg.2010.00170
Casseday, J. H., Ehrlich, D., & Covey, E. (1994). Neural tuning for sound duration: Role of inhibitory mechanisms in the inferior colliculus. Science, 264(5160), 847-850. https://doi.org/10.1126/science.8171341
Corbett, J. E., Aydin, B., & Munneke, J. (2021). Adaptation to average duration. Attention Perception & Psychophysics, 83(3), 1190-1200. https://doi.org/10.3758/s13414-020-02134-8
Corbett, J. E., Oriet, C., & Rensink, R. A. (2006). The rapid extraction of numeric meaning. Vision Research, 46(10), 1559-1573. https://doi.org/10.1016/j.visres.2005.11.015
Corbett, J. E., Wurnitsch, N., Schwartz, A., & Whitney, D. (2012). An aftereffect of adaptation to mean size. Visual Cognition, 20(2), 211-231. https://doi.org/10.1080/13506285.2012.657261
Diedenhofen, B., & Musch, J. (2015). Cocor: A comprehensive solution for the statistical comparison of correlations. PLoS One, 10(4), e0121945. https://doi.org/10.1371/journal.pone.0121945
Duysens, J., Schaafsma, S., & Orban, G. (1996). Cortical off response tuning for stimulus duration. Vision Research, 36(20), 3243-3251. https://doi.org/10.1016/0042-6989(96)00040-5
Faul, F., Erdfelder, E., Buchner, A., & Lang, A. G. (2009). Statistical power analyses using G*power 3.1: Tests for correlation and regression analyses. Behavior Research Methods, 41(4), 1149-1160. https://doi.org/10.3758/BRM.41.4.1149
Faure, P. A., Fremouw, T., Casseday, J. H., & Covey, E. (2003). Temporal masking reveals properties of sound-evoked inhibition in duration-tuned neurons of the inferior colliculus. Journal of Neuroscience, 23(7), 3052-3065. https://doi.org/10.1523/JNEUROSCI.23-07-03052.2003
Harvey, B. M., Dumoulin, S. O., Fracasso, A., & Paul, J. M. (2020). A network of topographic maps in human association cortex hierarchically transforms visual timing-selective responses. Current Biology, 30(8), 1424-1434. https://doi.org/10.1016/j.cub.2020.01.090
Hayashi, M. J., Ditye, T., Harada, T., Hashiguchi, M., Sadato, N., Carlson, S., Walsh, V., & Kanai, R. (2015). Time adaptation shows duration selectivity in the human parietal cortex. PLoS Biology, 13(9), e1002262. https://doi.org/10.1371/journal.pbio.1002262
Hayashi, M. J., & Ivry, R. B. (2020). Duration selectivity in right parietal cortex reflects the subjective experience of time. Journal of Neuroscience, 40(40), 7749-7758. https://doi.org/10.1523/JNEUROSCI.0078-20.2020
Hayashi, M. J., van der Zwaag, W., Bueti, D., & Kanai, R. (2018). Representations of time in human frontoparietal cortex. Communications Biology, 1, 233. https://doi.org/10.1038/s42003-018-0243-z
Heron, J., Aaen-Stockdale, C., Hotchkiss, J., Roach, N. W., McGraw, P. V., & Whitaker, D. (2012). Duration channels mediate human time perception. Proceedings of the Royal Society B: Biological Sciences, 279(1729), 690-698. https://doi.org/10.1098/rspb.2011.1131
Heron, J., Hotchkiss, J., Aaen-Stockdale, C., Roach, N. W., & Whitaker, D. (2013). A neural hierarchy for illusions of time: Duration adaptation precedes multisensory integration. Journal of Vision, 13(14), 1-12. https://doi.org/10.1167/13.14.4
Johnston, A., Arnold, D. H., & Nishida, S. (2006). Spatially localized distortions of event time. Current Biology, 16(5), 472-479. https://doi.org/10.1016/j.cub.2006.01.032
Kanai, R., Paffen, C. L. E., Hogendoorn, H., & Verstraten, F. A. J. (2006). Time dilation in dynamic visual display. Journal of Vision, 6, 1421-1430. https://doi.org/10.1167/6.12.8
Li, B., Chen, L., & Fang, F. (2019). Somatotopic representation of tactile duration: Evidence from tactile duration aftereffect. Behavioural Brain Research, 371, 111954. https://doi.org/10.1016/j.bbr.2019.111954
Li, B., Chen, Y., Xiao, L., Liu, P., & Huang, X. (2017). Duration adaptation modulates EEG correlates of subsequent temporal encoding. NeuroImage, 147, 143-151. https://doi.org/10.1016/j.neuroimage.2016.12.015
Li, B., Xiao, L., Yin, H., Liu, P., & Huang, X. (2017). Duration aftereffect depends on the duration of adaptation. Frontiers in Psychology, 8, 491. https://doi.org/10.3389/fpsyg.2017.00491
Li, B., Yuan, X., Chen, Y., Liu, P., & Huang, X. (2015). Visual duration aftereffect is position invariant. Frontiers in Psychology, 6, 1536. https://doi.org/10.3389/fpsyg.2015.01536
Li, B., Yuan, X., & Huang, X. (2015). The aftereffect of perceived duration is contingent on auditory frequency but not visual orientation. Scientific Reports, 5, 10124. https://doi.org/10.1038/srep10124
Maarseveen, J., Hogendoorn, H., Verstraten, F. A., & Paffen, C. L. (2016). An investigation of the spatial selectivity of the duration after-effect. Vision Research, 130, 67-75. https://doi.org/10.1016/j.visres.2016.11.003
Ortega, L., Guzman-Martinez, E., Grabowecky, M., & Suzuki, S. (2012). Flicker adaptation of low-level cortical visual neurons contributes to temporal dilation. Journal of Experimental Psychology: Human Perception and Performance, 38(6), 1380-1389. https://doi.org/10.1037/a0029495
Parkes, L., Lund, J., Angelucci, A., Solomon, J. A., & Morgan, M. (2001). Compulsory averaging of crowded orientation signals in human vision. Nature Neuroscience, 4(7), 739-744. https://doi.org/10.1038/89532
Protopapa, F., Hayashi, M. J., Kulashekhar, S., van der Zwaag, W., Battistella, G., Murray, M. M., Kanai, R., & Bueti, D. (2019). Chronotopic maps in human supplementary motor area. PLoS Biology, 17(3), e3000026. https://doi.org/10.1371/journal.pbio.3000026
Ren, Y., Allenmark, F., Muller, H. J., & Shi, Z. (2020). Logarithmic encoding of ensemble time intervals. Scientific Reports, 10, 18174. https://doi.org/10.1038/s41598-020-75191-6
Shi, Z., Church, R. M., & Meck, W. H. (2013). Bayesian optimization of time perception. Trends in Cognitive Sciences, 17(11), 556-564. https://doi.org/10.1016/j.tics.2013.09.009
Shi, Z., Ganzenmüller, S., & Müller, H. J. (2013). Reducing bias in auditory duration reproduction by integrating the reproduced signal. PLoS One, 8(4), e62065. https://doi.org/10.1371/journal.pone.0062065
Shima, S., Murai, Y., Hashimoto, Y., & Yotsumoto, Y. (2016). Duration adaptation occurs across the sub- and supra-second systems. Frontiers in Psychology, 7, 114. https://doi.org/10.3389/fpsyg.2016.00114
Stevens, F. L., Hurley, R. A., & Taber, K. H. (2011). Anterior cingulate cortex: Unique role in cognition and emotion. Journal of Neuropsychiatry and Clinical Neurosciences, 23(2), 120-125. https://doi.org/10.1176/jnp.23.2.jnp121
van Heukelum, S., Mars, R. B., Guthrie, M., Buitelaar, J. K., Beckmann, C. F., Tiesinga, P. H. E., Vogt, B. A., Glennon, J. C., & Havenith, M. N. (2020). Where is cingulate cortex? A cross-species view. Trends in Neurosciences, 43(5), 285-299. https://doi.org/10.1016/j.tins.2020.03.007
Walker, J. T., & Irion, A. L. (1979). Two new contingent aftereffects: Perceived auditory duration contingent on pitch and on temporal order. Perception & Psychophysics, 26(3), 241-244. https://doi.org/10.3758/bf03199875
Walker, J. T., Irion, A. L., & Gordon, D. G. (1981). Simple and contingent aftereffects of perceived duration in vision and audition. Perception & Psychophysics, 29(5), 475-486. https://doi.org/10.3758/bf03207361
Watamaniuk, S. N., Sekuler, R., & Williams, D. W. (1989). Direction perception in complex dynamic displays: The integration of direction information. Vision Research, 29(1), 47-59. https://doi.org/10.1016/0042-6989(89)90173-9
Yan, C. G., Wang, X. D., Zuo, X. N., & Zang, Y. F. (2016). DPABI: Data processing & analysis for (resting-state) brain imaging. Neuroinformatics, 14(3), 339-351. https://doi.org/10.1007/s12021-016-9299-4

Auteurs

Baolin Li (B)

School of Psychology, Shaanxi Normal University, Xi'an, China.
Faculty of Psychology, Southwest University, Chongqing, China.

Lijuan Xiao (L)

Institute of Social Psychology, School of Humanities and Social Sciences, Xi'an Jiaotong University, Xi'an, China.

Qinlin Yu (Q)

School of Life Sciences, Peking University, Beijing, China.

Xiting Huang (X)

Faculty of Psychology, Southwest University, Chongqing, China.

Classifications MeSH