Eye movements alter visual perceptions in a number of ways. During smooth-pursuit eye movements, previous studies reported decreased detection threshold for colored stimuli and for high-spatial-frequency luminance stimuli, suggesting a boost in the parvocellular system. The present study investigated the underlying neural mechanism using EEG in human participants. Participants followed a moving target with smooth-pursuit eye movements while steady-state visually evoked potentials (SSVEPs) were elicited by equiluminant red-green flickering gratings in the background. SSVEP responses to colored gratings were 18.9% higher during smooth pursuit than during fixation. There was no enhancement of SSVEPs by smooth pursuit when the flickering grating was defined by luminance instead of color. This result provides physiological evidence that the chromatic response in the visual system is boosted by the execution of smooth-pursuit eye movements in humans. Because the response improvement is thought to be the result of an improved response in the parvocellular system, SSVEPs to equiluminant stimuli could provide a direct test of parvocellular signaling, especially in populations where collecting an explicit behavioral response from the participant is not feasible. We constantly move our eyes when we explore the world. Eye movements alter visual perception in various ways. The smooth-pursuit eye movements have been shown to boost color sensitivity. We recorded steady-state visually evoked potentials to equiluminant chromatic flickering stimuli and observed increased steady-state visually evoked potentials when participants smoothly pursued a moving target compared with when they maintained fixation. This work provides direct neurophysiological evidence for the parvocellular boost by smooth-pursuit eye movements in humans.

When human observers track the movements of their own hand with their gaze, the eyes can start moving before the finger (i.e., anticipatory smooth pursuit). The signals driving anticipation could come from motor commands during finger motor execution or from motor intention and decision processes associated with self-initiated movements. For the present study, we built a mechanical device that could move a visual target either in the same direction as the participant's hand or in the opposite direction. Gaze pursuit of the target showed stronger anticipation if it moved in the same direction as the hand compared with the opposite direction, as evidenced by decreased pursuit latency, increased positional lead of the eye relative to target, increased pursuit gain, decreased saccade rate, and decreased delay at the movement reversal. Some degree of anticipation occurred for incongruent pursuit, indicating that there is a role for higher-level movement prediction in pursuit anticipation. The fact that anticipation was larger when target and finger moved in the same direction provides evidence for a direct coupling between finger and eye motor commands.

Our visual system maintains a stable representation of object size when viewing distance, and thus retinal size, changes. Previous studies have revealed that the extent of an object's representation in V1 shows systematic deviations from strict retinotopy when the object is perceived to be at different distances. It remains unknown, however, to what degree V1 activity accounts for perceptual size constancy. We investigated the neural correlates of size-constancy using steady-state visually evoked potentials (SSVEP) known to originate in early visual cortex. Flickering stimuli of various sizes were placed at a viewing distance of 40 cm and stimuli twice as large were shown at 80 cm. Thus both sets of stimuli had identical retinal sizes. At a constant viewing distance, SSVEP amplitude increased as a function of increasing retinal size. Crucially, SSVEP was larger when stimuli of a given retinal size were presented at 80 cm compared with at 40 cm independent of flicker frequency. Experiments were repeated and extended in virtual reality. Our results agree with previous findings showing that V1 activity plays a role in size constancy. Furthermore, we estimated the degree of the neural correction for the SSVEP as being close to 50% of the perceptual size constancy. This was the case in all experiments, independent of the effectiveness of perceptual size constancy. We conclude that retinotopy in V1 does get quite massively adjusted by perceived size, but not to the same extent as perceptual judgments.

Color vision in humans starts with three types of cones (short [S], medium [M], and long [L] wavelengths) in the retina and three retinal and subcortical cardinal mechanisms, which linearly combine cone signals into the luminance channel (L + M), the red-green channel (L – M), and the yellow-blue channel (S-(L + M)). Chromatic mechanisms at the cortical level, however, are less well characterized. The present study investigated such higher-order chromatic mechanisms by recording electroencephalograms (EEGs) on human observers in a noise masking paradigm. Observers viewed colored stimuli that consisted of a target embedded in noise. Color directions of the target and noise varied independently and systematically in an isoluminant plane of color space. The target was flickering on-off at 3 Hz, eliciting steady-state visual evoked potential (SSVEP) responses. As a result, the masking strength could be estimated from the SSVEP amplitude in the presence of 6 Hz noise. Masking was strongest (i.e. target eliciting smallest SSVEPs) when the target and noise were along the same color direction, and was weakest (i.e. target eliciting highest SSVEPs) when the target and noise were along orthogonal directions. This pattern of results was observed both when the target color varied along the cardinal and intermediate directions, which is evidence for higher-order chromatic mechanisms tuned to intermediate axes. The SSVEP result can be well predicted by a model with multiple broadly tuned chromatic mechanisms. In contrast, a model with only cardinal mechanisms failed to account for the data. These results provide strong electrophysiological evidence for multiple chromatic mechanisms in the early visual cortex of humans.