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Polti, I.

Publications and source records attributed to Polti, I..

2 recordsLinked to original sources

Episodic timing: how spontaneous alpha clocks, retrospectively

We seldom time life events intently yet recalling the duration of events is lifelike. Is episodic time the outcome of a rational after-thought or of physiological clocks keeping track of time without our conscious awareness of it? To answer this, we recorded human brain activity with magnetoencephalography (MEG) during quiet wakefulness. Unbeknownst to participants, we asked them after the MEG recording to guess its duration. In the absence of overt attention to time, the relative amount of time participants alpha brain rhythms ( ~10 Hz) were in bursting mode predicted participants retrospective duration estimate. This relation was absent when participants prospectively measured elapsed time during the MEG recording. We conclude that bursts embody discrete states of awareness for episodic timing. One-Sentence SummaryIn the human brain, the relative number of alpha oscillatory bursts at ~10 Hz can tell time when the observer does not attend to it.

neuroscience↗

Hippocampus and striatum encode distinct task regularities that guide human timing behavior

The brain encodes the statistical regularities of the environment in a task-specific yet flexible and generalizable format. Here, we seek to understand this process by converging two parallel lines of research, one centered on sensorimotor timing, and the other on cognitive mapping in the hippocampal system. By combining functional magnetic resonance imaging (fMRI) with a fastpaced time-to-contact (TTC) estimation task, we found that the hippocampus signaled behavioral feedback received in each trial as well as performance improvements across trials along with reward-processing regions. Critically, it signaled performance improvements independent from the tested intervals, and its activity accounted for the trial-wise regression-to-the-mean biases in TTC estimation. This suggests that the hippocampus supports the rapid encoding of temporal context even on short time scales in a behavior-dependent manner. Our results emphasize the central role of the hippocampus in statistical learning and position it at the core of a brain-wide network updating sensorimotor representations in real time for flexible behavior.

neuroscience↗