Abstract:The present study uses simple reaction time (RT) to examine the temporal response to chromatic changes of the red-green (L-2M) and yellow-blue (S-(LϩM
“…8,21,22,[24][25][26][28][29][30] Both subjects had normal color vision (according to the Ishihara test, Pickford-Nicholson anomaloscopy, and Dichotomique Farnsworth 15D test) and normal stereopsis (according to stereo-fly tests). Observer MC was inexperienced while observer JA was highly experienced in VRT experiments.…”
Section: A Observersmentioning
confidence: 99%
“…To produce the stimuli with particular CIE-1931 coordinates and luminance, we used a modified calibration method of Post and Calhoun. 21,36,37 Observers were seated 70 cm from the CRT in a dark room and used a chin rest for head stabilization.…”
Section: B Apparatus and Calibrationmentioning
confidence: 99%
“…Simple reaction times, defined as the time that elapses from stimulus presentation until an observer's response is registered 19,20 (e.g., by pressing a key), offer the noteworthy possibility of exploring the relationship between visual latencies and their underlying physiological background for the whole eye-brain-hand system at suprathreshold conditions. 8,[19][20][21][22][23] Previous works have found that chromatic adaptation influences perceived contrast, producing selectivity changes along cardinal and intermediate color axes on the isoluminant plane. 8 Thus, it was found that mean visual-reaction times (VRTs) for contrast changes are sensitive to the chromatic-adaptation level evaluated in terms of Stiles's mechanisms or for both cardinal and noncardinal color axes on the isoluminance plane.…”
Section: Introductionmentioning
confidence: 99%
“…8 Thus, it was found that mean visual-reaction times (VRTs) for contrast changes are sensitive to the chromatic-adaptation level evaluated in terms of Stiles's mechanisms or for both cardinal and noncardinal color axes on the isoluminance plane. 8,21,22,24 In the present study, we use simple visual-reaction times (VRTs) as an alternative technique to study the temporal process in contrast detection after chromatic adaptation. We develop two levels of analysis.…”
Section: Introductionmentioning
confidence: 99%
“…Taking into account Piéron's law in terms of the RMS cone contrast scaled in threshold units, mean reaction times increased as the RMS cone contrast decreased. 19,21,22 Thus, if a single function account for all the data in the red-green direction under different adapting conditions, contrast detection will not be affected by the level of chromatic adaptation adopted, so that we can assume the existence of a single adaptive stage in the LϪM-cone system, presumably at the photoreceptor level. In the contrary case, if a single function fit each LϪM axis better under each adapting condition, contrast detection is influenced by the level of chromatic adaptation, and thus first-and secondsite adaptive processes should be considered within the red-green chromatic-opponent mechanism, the latter presumably associated at the postreceptoral level (analogously for the S-cone system).…”
(Doc. ID 62073) Simple visual-reaction times (VRT) were measured for a variety of stimuli selected along red-green (L − M axis) and blue-yellow [S − ͑L+M͒ axis] directions in the isoluminant plane under different adaptation stimuli. Data were plotted in terms of the RMS cone contrast in contrast-threshold units. For each opponent system, a modified Piéron function was fitted in each experimental configuration and on all adaptation stimuli. A single function did not account for all the data, confirming the existence of separate postreceptoral adaptation mechanisms in each opponent system under suprathreshold conditions. The analysis of the VRT-hazard functions suggested that both color-opponent mechanisms present a well-defined, transient-sustained structure at marked suprathreshold conditions. The influence of signal polarity and chromatic adaptation on each color axis proves the existence of asymmetries in the integrated hazard functions, suggesting separate detection mechanisms for each pole (red, green, blue, and yellow detectors).
“…8,21,22,[24][25][26][28][29][30] Both subjects had normal color vision (according to the Ishihara test, Pickford-Nicholson anomaloscopy, and Dichotomique Farnsworth 15D test) and normal stereopsis (according to stereo-fly tests). Observer MC was inexperienced while observer JA was highly experienced in VRT experiments.…”
Section: A Observersmentioning
confidence: 99%
“…To produce the stimuli with particular CIE-1931 coordinates and luminance, we used a modified calibration method of Post and Calhoun. 21,36,37 Observers were seated 70 cm from the CRT in a dark room and used a chin rest for head stabilization.…”
Section: B Apparatus and Calibrationmentioning
confidence: 99%
“…Simple reaction times, defined as the time that elapses from stimulus presentation until an observer's response is registered 19,20 (e.g., by pressing a key), offer the noteworthy possibility of exploring the relationship between visual latencies and their underlying physiological background for the whole eye-brain-hand system at suprathreshold conditions. 8,[19][20][21][22][23] Previous works have found that chromatic adaptation influences perceived contrast, producing selectivity changes along cardinal and intermediate color axes on the isoluminant plane. 8 Thus, it was found that mean visual-reaction times (VRTs) for contrast changes are sensitive to the chromatic-adaptation level evaluated in terms of Stiles's mechanisms or for both cardinal and noncardinal color axes on the isoluminance plane.…”
Section: Introductionmentioning
confidence: 99%
“…8 Thus, it was found that mean visual-reaction times (VRTs) for contrast changes are sensitive to the chromatic-adaptation level evaluated in terms of Stiles's mechanisms or for both cardinal and noncardinal color axes on the isoluminance plane. 8,21,22,24 In the present study, we use simple visual-reaction times (VRTs) as an alternative technique to study the temporal process in contrast detection after chromatic adaptation. We develop two levels of analysis.…”
Section: Introductionmentioning
confidence: 99%
“…Taking into account Piéron's law in terms of the RMS cone contrast scaled in threshold units, mean reaction times increased as the RMS cone contrast decreased. 19,21,22 Thus, if a single function account for all the data in the red-green direction under different adapting conditions, contrast detection will not be affected by the level of chromatic adaptation adopted, so that we can assume the existence of a single adaptive stage in the LϪM-cone system, presumably at the photoreceptor level. In the contrary case, if a single function fit each LϪM axis better under each adapting condition, contrast detection is influenced by the level of chromatic adaptation, and thus first-and secondsite adaptive processes should be considered within the red-green chromatic-opponent mechanism, the latter presumably associated at the postreceptoral level (analogously for the S-cone system).…”
(Doc. ID 62073) Simple visual-reaction times (VRT) were measured for a variety of stimuli selected along red-green (L − M axis) and blue-yellow [S − ͑L+M͒ axis] directions in the isoluminant plane under different adaptation stimuli. Data were plotted in terms of the RMS cone contrast in contrast-threshold units. For each opponent system, a modified Piéron function was fitted in each experimental configuration and on all adaptation stimuli. A single function did not account for all the data, confirming the existence of separate postreceptoral adaptation mechanisms in each opponent system under suprathreshold conditions. The analysis of the VRT-hazard functions suggested that both color-opponent mechanisms present a well-defined, transient-sustained structure at marked suprathreshold conditions. The influence of signal polarity and chromatic adaptation on each color axis proves the existence of asymmetries in the integrated hazard functions, suggesting separate detection mechanisms for each pole (red, green, blue, and yellow detectors).
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