A population readout of extrastriate activity reveals biased and smoothed temporal representations across saccades.

Perception of visual time is transiently distorted around saccadic eye movements, yet the neuronal mechanisms constructing perisaccadic representations of time remain unclear. Here, we investigate how perisaccadic temporal information is encoded and read out in extrastriate cortex, by combining electrophysiological recordings in V4 and MT neuronal population in macaque monkeys under high spatiotemporal resolution visual stimulation, and a statistical modeling framework capturing perisaccadic response modulations at single-trial precision. Our analyses show that perisaccadic neuronal responses systematically shift the temporal representation of presaccadic stimuli within receptive fields-biasing them toward earlier times, and also reduce temporal sensitivity for presaccadic stimuli-impairing discrimination of stimulus onset times. Model-based readout using time-varying spatiotemporal sensitivity maps in neuronal ensembles enables quantitative characterization of these effects and identifies their specific neuronal response components at millisecond resolution. In silico manipulations further demonstrate a causal role of representational bias in reducing temporal sensitivity. These findings suggest that extrastriate cortex implements an active encoding strategy to stabilize presaccadic temporal information by favoring the most recent reliable input, revealing a fundamental tradeoff between temporal precision and robustness that supports a continuous visual percept across saccades. This finding also establishes a general role for extrastriate populations in constructing the perception of visual time.