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Journal ArticleDOI

Color vision in the peripheral retina. II. Hue and saturation

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TLDR
From a modified form of color matching, it was concluded that the color deficiency in the periphery is more tritanlike than deutanlike, strengthened by the observation, that, for small peripheral targets, hues are generally apportioned between two hue categories and the change from one to the other is at about 580 nm.
Abstract
Hue and saturation of spectral lights were measured (direct scaling) in the fovea and at 45° in the periphery; all lights were of equal photopic retinal illuminance (1200 trolands). At each retinal location both large and small targets were used. As shown by previous studies, small peripheral targets appear desaturated and of uncertain hue, except long wavelengths which appear red. However, if target size is increased, saturation increases and a full range of hues is seen; the hue functions for large peripheral targets are comparable to foveal ones for very small targets. From a modified form of color matching, it was concluded that the color deficiency in the periphery is more tritanlike than deutanlike; this is strengthened by the observation that, for small peripheral targets, hues are generally apportioned between two hue categories and the change from one to the other is at about 580 nm.

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Citations
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Journal ArticleDOI

Cat and monkey retinal ganglion cells and their visual functional roles

TL;DR: Comparisons between cat and monkey ganglion cell classes reveal several important similarities between M cells and X cells, which are very sensitive to contrast.
Journal ArticleDOI

Functional anatomy of macaque striate cortex. III. Color

TL;DR: The DG results suggest that color sensitivity is also high in the lower-layer (layers 5 + 6) blobs, and that many layer 5 receptive fields are double-opponent, which supports the idea of a color-insensitive stream running from the magnocellular LGN layers through striate layers 4Ca and 4B to extrastriate areas MT and V3.
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Visual resolution, contrast sensitivity, and the cortical magnification factor

TL;DR: The results indicated specificly that visual patterns can be made equally visible if they are scaled so that their calculated cortical representations become equivalent and the power law of spatial summation suggests the existence of a central integrator that pools the activity of cortical neurons.
Journal ArticleDOI

Organization of the Human Trichromatic Cone Mosaic

TL;DR: The results suggest that the assignment of L and M pigment, although highly irregular, is not a completely random process, and in the protan carrier, there was no evidence of clumping, perhaps as a result of cone migration during foveal development.
References
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Journal ArticleDOI

Bezold–Brücke Hue Shift Measured by Color-Naming Technique*

TL;DR: In this article, three experiments on the Bezold-Brucke phenomenon are reported: an exact replication of Purdy's classic experiment, where the shift between 100 and 1000 trolands is investigated by direct matching in a steadily presented bipartite field.
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Colour Sensitivity of the Fovea Centralis

TL;DR: A small central area of the fovea was unable to discriminate blue-green colours and, in other ways also, appeared to have the characteristics of the tritanopic form of colour-blindness.
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Hue-Wavelength Relation Measured by Color-Naming Method for Three Retinal Locations

TL;DR: A method of hue measurement has been applied to spectral stimuli delivered as flashes at 0 degrees, 20 degrees, and 40 degrees eccentricity in an otherwise dark field, and results showed a decrease in measured saturation but increasing reliability of the saturation measurements with increasing eccentricity.
Journal ArticleDOI

Colour Perception with the Peripheral Retina

TL;DR: The results indicate a progressive deterioration in colour perception with distance from the fovea: tending, under the conditions of the experiment, to dichromatism at 25°-30° and to monochromatismAt 40°–50°.
Journal ArticleDOI

Rod participation in the ‘blue’ mechanism and its effect on colour matching

TL;DR: An enquiry into why “rod colour” should be blue, together with an examination of the similarities and dissimilarities of rods and “blue cones”, leads to the further suggestion that rods and "blue cones" exist separately but share a neural pathway.
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