We investigated whether the monkey superior colliculus (SC), an important midbrain structure for the regulation of saccadic eye movements, contains neurons with activity patterns sufficient to control both the cancellation and the production of saccades. We used a countermanding task to manipulate the probability that, after the presentation of a stop signal, the monkeys canceled a saccade that...

The lateral intraparietal area (LIP), a region of posterior parietal cortex, was once thought to be unresponsive to auditory stimulation. However, recent reports have indicated that neurons in area LIP respond to auditory stimuli during an auditory-saccade task. To what extent are auditory responses in area LIP dependent on the performance of an auditory-saccade task? To address this question, ...

Whenever the eyes move, spatial attention must keep track of the locations of targets as they shift on the retina. This study investigated transsaccadic updating of visual attention to cued targets. While observers prepared a saccade, we flashed an irrelevant, but salient, color cue in their visual periphery and measured the allocation of spatial attention before and after the saccade using a t...

A distractor placed nearby a saccade target will cause interference during saccade planning and execution, and as a result will cause the saccade's trajectory to curve in a systematic way. It has been demonstrated that making a distractor more task-relevant, for example by increasing its similarity to the target, will increase the interference it imposes on the saccade and generate more deviant...

Electroencephalogram (EEG) related to fast eye movement (saccade), has been the subject of application oriented research by our group toward developing a brain-computer interface(BCI). Our goal is to develop novel BCI based on eye movements system employing EEG signals on-line. Most of the analysis of the saccade-related EEG data has been performed using ensemble averaging approaches. However, ...

A biophysical cortico-colicular model of saccade initiation based on competitive integration of planned and reactive cortical saccade decision signals in the intermediate layer of the superior colliculus is introduced. The variable slopes of the climbing activities of the input cortical decision signals are produced from variability in the ionic and synaptic conductances of cortical neurons. Th...

We recorded saccadic eye movements in patients mildly affected with Huntington's disease. Most showed an increase in saccade latencies that was greater for saccades made on command than to the sudden appearance of a visual target. All patients showed excessive distractibility during attempted fixation. They had particular difficulty suppressing a saccade to a suddenly appearing visual target wh...

The present paper reports results of a dual task study in which two locations were endogenously cued as possible target locations, while only one eye movement had to be executed. During the cue period, letters were briefly presented at the saccade goals and at no-saccade goals. Results show that performance was better for letters presented at any of the saccade goals than for letters presented ...

1. In the companion paper we reported that the predominant signal of the population of neurons in the lateral intraparietal area (area LIP) of the monkey's posterior parietal cortex (PPC) encode the next intended saccadic eye movement during the delay period of a memory-saccade task. This result predicts that, should be monkey change his intention of what the next saccade will be, LIP activity ...

Saccade planning may invoke spatially-specific feedback signals that bias early visual activity in favor of top-down goals. We tested this hypothesis by measuring cortical activity at the early stages of the dorsal and ventral visual processing streams. Human subjects maintained saccade plans to (prosaccade) or away (antisaccade) from a spatial location over long memory-delays. Results show tha...