Since Hick's original description, many subsequent studies have confirmed the logarithmic relationship that exists between response time and the number of alternatives (NA) for a choice response. In the present study a novel paradigm was used to quantify saccade response time as a function of NA. Normal subjects were required to make a saccade to the remembered location of a visual target whose color was specified by a centrally located cue. The paradigm thus required a stimulus-response transformation similar to that used by Hick. The results show that, when such a transformation was required, a logarithmic relationship was found for saccadic response time. The use of a color-to-location paradigm to study saccade choice response time produ...
We describe a novel behavioral method to accurately discriminate anticipatory (i.e., saccades not ge...
The neural basis of choice behavior is commonly investigated with tasks in which a subject analyzes ...
AbstractWe used a countermanding paradigm to investigate the relationship between conflicting cues f...
When exploring the visual environment, one uses saccades to shift gaze and fixation to gather spatia...
One of the most common decisions we make is the one about where to move our eyes next. Here we exami...
In action sequences, the eyes are generally fixated ahead of the stimulus being responded to, overla...
Abstract That saccadic reaction times (SRTs) may depend on reinforcement contingencies has been repe...
International audiencePrevious studies have shown that face stimuli elicit extremely fast and involu...
In the antisaccade paradigm subjects are instructed to perform eye movements in the opposite directi...
Sensory information travels to visual and motor areas via several distinct pathways, some of them be...
International audienceAction decisions are considered an emergent property of competitive response a...
Models of perceptual decision making often assume that sensory evidence is accumulated over time in ...
In the classic double-step paradigm, subjects are required to make a saccade to a visual target that...
We describe a novel behavioral method to accurately discriminate anticipatory (i.e., saccades not ge...
The neural basis of choice behavior is commonly investigated with tasks in which a subject analyzes ...
AbstractWe used a countermanding paradigm to investigate the relationship between conflicting cues f...
When exploring the visual environment, one uses saccades to shift gaze and fixation to gather spatia...
One of the most common decisions we make is the one about where to move our eyes next. Here we exami...
In action sequences, the eyes are generally fixated ahead of the stimulus being responded to, overla...
Abstract That saccadic reaction times (SRTs) may depend on reinforcement contingencies has been repe...
International audiencePrevious studies have shown that face stimuli elicit extremely fast and involu...
In the antisaccade paradigm subjects are instructed to perform eye movements in the opposite directi...
Sensory information travels to visual and motor areas via several distinct pathways, some of them be...
International audienceAction decisions are considered an emergent property of competitive response a...
Models of perceptual decision making often assume that sensory evidence is accumulated over time in ...
In the classic double-step paradigm, subjects are required to make a saccade to a visual target that...
We describe a novel behavioral method to accurately discriminate anticipatory (i.e., saccades not ge...
The neural basis of choice behavior is commonly investigated with tasks in which a subject analyzes ...
AbstractWe used a countermanding paradigm to investigate the relationship between conflicting cues f...