Pre-stimulus pupil-linked arousal enhances initial stimulus availability and accelerates decay in iconic memory

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Abstract

Pupil diameter reflects not only reflexive responses to light but also spontaneous fluctuations in arousal. Such pre-stimulus fluctuations may shape visual performance, yet it remains unclear whether they only affect perceptual sensitivity or decision processes in near-threshold tasks, or instead influence the temporal availability of sensory information even for highly visible stimuli. We tested whether pupil-linked arousal modulates iconic memory, a high-capacity but short-lived visual store bridging sensory encoding and short-term memory. Based on a model in which a brief stimulus evokes an internal response decaying over a few hundred milliseconds, we hypothesized that increased arousal enhances performance either by amplifying the initial response or by slowing its decay. Thirty-seven participants viewed brief displays of six oriented stimuli, followed by a cue after a variable stimulus–cue onset asynchrony indicating which item to report. Pre-stimulus pupil diameter was continuously recorded, and behavioral data were fitted with an exponential decay function estimating initial stimulus availability, decay rate, and asymptotic performance. Larger pre-stimulus pupil dilation was associated with higher initial stimulus availability but faster decay of the iconic trace, while information transferred into short-term memory and confidence ratings remained unaffected. These findings demonstrate that spontaneous fluctuations in arousal shape the temporal dynamics of sensory persistence. Elevated arousal boosts the initial strength of visual representations but shortens their duration, suggesting that arousal adaptively prioritizes rapid updating of visual input over prolonged stability.

Significance Statement

How does arousal shape the earliest stages of visual memory? By leveraging a criterion-free partialreport task that emphasizes the temporal availability of sensory information, we show that spontaneous pre-stimulus pupil dilation – an index of arousal – selectively boosts the initial availability of iconic memory while accelerating its decay. This dual effect suggests that arousal tunes the temporal dynamics of sensory persistence, potentially prioritizing rapid updating of incoming information. These findings advance the understanding of how state-dependent fluctuations in arousal shape early perception in a context that minimizes decision-bias confounds.

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