Abstract
Our eyes are in constant motion, yet we perceive the visual world as stable. Predictive remapping of receptive fields is thought to be one of the critical mechanisms for enforcing perceptual stability during eye movements. While receptive field remapping has been identified in several cortical areas, the spatiotemporal dynamics of remapping, and its consequences on the tuning properties of neurons, remain poorly understood. Here, we tracked remapping receptive fields in hundreds of neurons from visual Area V2 while subjects performed a cued saccade task. We found that remapping was far more widespread in Area V2 than previously reported and can be found in neurons from all recorded cortical layers and cell types. Surprisingly, neurons undergoing remapping exhibit sensitivity to two punctate locations in visual space. Furthermore, we found that feature selectivity is not only maintained during remapping but transiently increases due to untuned suppression. Taken together, these results shed light on the spatiotemporal dynamics of remapping and its ubiquitous prevalence in the early visual cortex, and force us to revise current models of perceptual stability.