RESUMEN
Hue-discrimination functions were derived from hue-naming data (480-620 nm, 20 nm steps) obtained in 4 min intervals from 4 min to 28 min postbleach at 10° temporal retinal eccentricity. Hue-naming data were also obtained in the fovea. Hue-discrimination functions derived at the 4, 8, and 12 min intervals were very similar to those derived in the fovea. As time postbleach exceeded 12 min and rod sensitivity increased, the shape of the hue-discrimination functions changed. Most notably, the minimum between 560-580 nm disappeared and the just noticeable differences (JNDs) for the longer wavelength stimuli increased. The long-wavelength suppression in hue discrimination may be due to rod input in the magnocellular pathway interacting and affecting the long-wavelength sensitivity of the parvocellular pathway.
RESUMEN
BACKGROUND: Studies investigating the effect of rods on unique hue loci in the peripheral retina generally obtain measures at two time points associated with the dark adaptation function - the cone plateau and the rod plateau. In comparison, this study used a color-naming procedure to identify the loci of unique green and unique yellow as a function of time associated with the entire dark adaptation function. The unique hue loci derived by this procedure were then compared to those obtained directly with a staircase procedure. METHOD: Hue-scaling functions were obtained for monochromatic stimuli for four observers using the '4 + 1' procedure. Data were collected every 4 min following extinction of a bleaching stimulus. These hue-scaling functions were then converted to uniform appearance diagrams (UADs) to derive unique green and unique yellow loci. Unique green and unique yellow loci were also obtained from the same observers via a staircase procedure at 4-9 min post-bleach (minimal rod input) and after 28 min dark adaptation (maximal rod input). Measurements were made in the peripheral retina at 10° temporal retinal eccentricity and at the fovea. RESULTS: Unique green loci derived from UADs are at longer wavelengths compared to those measured directly with the staircase procedure. In addition, unique green loci derived from UADs show a progressive shift to longer wavelengths as time post-bleach increases; whereas, unique green loci obtained from the staircase procedure differ little between the rod-bleach and no-bleach conditions. Unique yellow loci are similar across both experimental procedures. CONCLUSION: Unique green loci derived from UADs are not the same as those measured with traditional psychophysical procedures. These differences may be due to the different response criteria used by observers in the color-naming and staircase procedures. The unique green loci obtained from UADs indicate that rod signals shift unique green loci to longer wavelengths as time post-bleach increases. More direct methods need to be employed to determine if this rod effect is valid.