Although numerous studies have examined the relationship between smooth-pursuit eye movements and motion perception, it remains unresolved whether a common motion-processing system subserves both perception and pursuit. To address this question, we simultaneously recorded perceptual direction judgments and the concomitant smooth eye-movement response to a plaid stimulus that we have previously ...

The primate frontal cortex contains two areas related to smooth-pursuit: the frontal eye fields (FEFs) and supplementary eye fields (SEFs). To distinguish the specific role of the SEFs in pursuit, we examined discharge of a total of 89 pursuit-related neurons that showed consistent modulation when head-stabilized Japanese monkeys pursued a spot moving sinusoidally in fronto-parallel planes and/...

When small objects move in a scene, we keep them foveated with smooth pursuit eye movements. Although large objects such as people and animals are common, it is nonetheless unknown how we pursue them since they cannot be foveated. It might be that the brain calculates an object's centroid, and then centers the eyes on it during pursuit as a foveation mechanism might. Alternatively, the brain me...

Visual sensitivity is dynamically modulated by eye movements. During saccadic eye movements, sensitivity is reduced selectively for low-spatial frequency luminance stimuli and largely unaffected for high-spatial frequency luminance and chromatic stimuli (Nature 371 (1994), 511-513). During smooth pursuit eye movements, sensitivity for low-spatial frequency luminance stimuli is moderately reduce...

The challenges in development of solid oxide fuel cells (SOFCs) are reducing their dimensions and increasing their efficiency and durability, which requires physicochemical characterization at micro-scales of the device components during operation conditions. Recently, the unique potential of scanning photoelectron microscopy (SPEM) has been demonstrated by in-situ studies of externally-driven ...

Two-dimensional sum-of-sines waveforms were pursued by the eye with very small phase delays compared with visual feedback delays estimated in the same monkeys. Processing delays in making smooth corrections averaged 90 msec after infrequent right-angle perturbations from a circular trajectory. These feedback delays were much larger than component phase delays during pursuit that averaged: 10 ms...

The development of the asymmetry between horizontal and vertical eye tracking was investigated longitudinally at 5, 7, and 9 months of age. The target moved either on a 2D circular trajectory or on a vertical or horizontal 1D sinusoidal trajectory. Saccades, smooth pursuit, and head movements were measured. Vertical tracking was found to be inferior to horizontal tracking at all age levels. The...

It is known that visual transients prolong saccadic latency and reduce saccadic frequency. The latter effect was attributed to subcortical structures because it occurred only 60-70 ms after stimulus onset. We examined the effects of large task-irrelevant transients on steady-state pursuit and the generation of catch-up saccades. Two screen-wide stripes of equal contrast (4, 20, or 100%) were br...

Saccades and smooth pursuit eye movements are two different modes of oculomotor control. Saccades are primarily directed toward stationary targets whereas smooth pursuit is elicited to track moving targets. In recent years, behavioural and neurophysiological data demonstrated that both types of eye movements work in synergy for visual tracking. This suggests that saccades and pursuit are two ou...

Primates are able to track small moving visual targets using smooth pursuit eye movements. Target motion for smooth pursuit is signaled by neurons in visual cortical areas MT and MST. In this study, we trained monkeys to either initiate or withhold smooth pursuit in the presence of a moving target to test whether this decision was reflected in the relative strength of "go" and "no-go" processes...