Abstract

Eye movements create an ever-changing image of the world on the retina. In particular, frequent saccades call for a compensatory mechanism to transform the changing visual information into a stable percept. To this end, the brain presumably uses internal copies of motor commands. Electrophysiological recordings of visual neurons in the primate lateral intraparietal cortex, the frontal eye fields, and the superior colliculus suggest that the receptive fields (RFs) of special neurons shift towards their post-saccadic positions before the onset of a saccade. However, the perceptual consequences of these shifts remain controversial. We wanted to test in humans whether a remapping of motion adaptation occurs in visual perception.The motion aftereffect (MAE) occurs after viewing of a moving stimulus as an apparent movement to the opposite direction. We designed a saccade paradigm suitable for revealing pre-saccadic remapping of the MAE. Indeed, a transfer of motion adaptation from pre-saccadic to post-saccadic position could be observed when subjects prepared saccades. In the remapping condition, the strength of the MAE was comparable to the effect measured in a control condition (33±7% vs. 27±4%). Contrary, after a saccade or without saccade planning, the MAE was weak or absent when adaptation and test stimulus were located at different retinal locations, i.e. the effect was clearly retinotopic.Regarding visual cognition, our study reveals for the first time predictive remapping of the MAE but no spatiotopic transfer across saccades. Since the cortical sites involved in motion adaptation in primates are most likely the primary visual cortex and the middle temporal area (MT/V5) corresponding to human MT, our results suggest that pre-saccadic remapping extends to these areas, which have been associated with strict retinotopy and therefore with classical RF organization. The pre-saccadic transfer of visual features demonstrated here may be a crucial determinant for a stable percept despite saccades.

Highlights

  • When we move our eyes, the resulting retinal slip cannot be distinguished from global movement of the surrounding environment at the retinal input level

  • Regarding saccades it has been suggested by Sommer and Wurtz that in monkeys a pathway originating from the superior colliculus (SC), passing through mediodorsal thalamus, reaching cortex at the frontal eye field, carries the efference copy signal [8]

  • We report the presence of a motion aftereffect (MAE) in a visual remapping paradigm

Read more

Summary

Introduction

When we move our eyes, the resulting retinal slip cannot be distinguished from global movement of the surrounding environment at the retinal input level. Regarding saccades it has been suggested by Sommer and Wurtz that in monkeys a pathway originating from the superior colliculus (SC), passing through mediodorsal thalamus, reaching cortex at the frontal eye field, carries the efference copy signal [8] In their experiments a special task that necessitates internal monitoring of saccades called the double-step task [9,10] was used. Later experiments by Sommer and Wurtz [27] investigating properties of neurons in the saccadic subregion of the cortical frontal eye field (FEFsac) of macaque monkeys demonstrated that these neurons show impaired visual processing, i.e. defective remapping, when the mediodorsal thalamus, supposedly the relay station for the efference copy signals, was temporarily inactivated. This suggests that the remapping mechanism is a crucial component for conveying visual constancy

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call