Spontaneous Oscillatory Activity in Episodic Timing: An EEG Replication Study and Its Limitations

Episodic timing refers to the one-shot, automatic encoding of temporal information in the brain, in the absence of attention to time. A previous magnetoencephalography (MEG) study showed that the relative burst time of spontaneous alpha oscillations (α) during quiet wakefulness was a selective predictor of retrospective duration estimation. This observation was interpreted as α embodying the "ticks" of an internal contextual clock. Herein, we replicate and extend these findings using electroencephalography (EEG), assess robustness to time-on-task effects, and test the generalizability in virtual reality (VR) environments. In three EEG experiments, 128 participants of either sex underwent 4 min eyes-open resting-state recordings followed by an unexpected retrospective duration estimation task. Experiment 1 tested participants before any tasks, Experiment 2 after 90 min of timing tasks, and Experiment 3 in VR environments of different sizes. We successfully replicated the original MEG findings in Experiment 1 but did not in Experiment 2. We explain the lack of replication through time-on-task effects (changes in α power and topography) and contextual changes yielding a cognitive strategy based on temporal expectation (supported by a fast passage of time). In Experiment 3, we did not find the expected duration underestimation in VR and did not replicate the correlation between α bursts and retrospective time estimates. Overall, while EEG captures the α burst marker of episodic timing, its reliability depends critically on experimental context. Our findings highlight the importance of controlling experimental context when using α bursts as a neural marker of episodic timing.

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Publication Details

Journal
eNeuro
Published
2026-01-01
DOI
https://doi.org/10.1523/eneuro.0332-25.2025
Citations
1
Primary Topic
Neuroscience and Music Perception
Type
article
Field-Weighted Citation Impact
29.71

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Spontaneous Oscillatory Activity in Episodic Timing: An EEG Replication Study and Its Limitations

Raphaël Bordas, Virginie van Wassenhove
1 citations
eNeuro
Neuroscience and Music Perception
29.71
article

Spontaneous Oscillatory Activity in Episodic Timing: An EEG Replication Study and Its Limitations

Raphaël Bordas, Virginie van Wassenhove
article en
1 citations

Abstract

Episodic timing refers to the one-shot, automatic encoding of temporal information in the brain, in the absence of attention to time. A previous magnetoencephalography (MEG) study showed that the relative burst time of spontaneous alpha oscillations (α) during quiet wakefulness was a selective predictor of retrospective duration estimation. This observation was interpreted as α embodying the "ticks" of an internal contextual clock. Herein, we replicate and extend these findings using electroencephalography (EEG), assess robustness to time-on-task effects, and test the generalizability in virtual reality (VR) environments. In three EEG experiments, 128 participants of either sex underwent 4 min eyes-open resting-state recordings followed by an unexpected retrospective duration estimation task. Experiment 1 tested participants before any tasks, Experiment 2 after 90 min of timing tasks, and Experiment 3 in VR environments of different sizes. We successfully replicated the original MEG findings in Experiment 1 but did not in Experiment 2. We explain the lack of replication through time-on-task effects (changes in α power and topography) and contextual changes yielding a cognitive strategy based on temporal expectation (supported by a fast passage of time). In Experiment 3, we did not find the expected duration underestimation in VR and did not replicate the correlation between α bursts and retrospective time estimates. Overall, while EEG captures the α burst marker of episodic timing, its reliability depends critically on experimental context. Our findings highlight the importance of controlling experimental context when using α bursts as a neural marker of episodic timing.

eNeuroVol. 13(1)
Inserm (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), Université Paris-Saclay (FR), CEA Paris-Saclay (FR), Cognitive Neuroimaging Lab (FR)
European Commission, Agence Nationale de la Recherche, Horizon 2020 Framework Programme
Openalex Percentile: Top 2%
Neuroscience and Music Perception
29.71
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