Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Color Vision”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,009 records · Page 56Linked to original sources
PubMed1966

Color vision in the adult female two-spotted spider mite.

Responses of the summer form of the adult female two-spotted spider mite, Tetranychus urticae Koch (Acarina: Tetranychoidea) placed in near-ultraviolet and green light are photopositive. The independent variation of these responses requires the presence of separate receptor systems.

Animals↗
PubMed1997

[Stimulation parameters for automatic examination of color vision].

PURPOSE: We have developed a polyvalent computer controlled instrument, which uses the "two equation method" (Rayleigh and Moreland equations) to measure human colour vision. This "colorimeter" (or anomaloscope) was used to determine the influence of some important stimulation parameters. METHODS: The influence of stimulus exposure time, observation field size, absolute stimulus luminance, saturation and luminance mismatches between mixture and reference stimuli were measured on our computer controlled colorimeter. All subjects were normal observers. RESULTS: 1) An exposure time of 2s was found to be optimal for clinical work. 2) The Moreland equation on a 7 degrees observation field yields results in which population variability is comparable to a Rayleigh equation on a 2 degrees field. 3) A retinal illuminance between 40 and 1000 trolands can be used for automated Moreland matches. 4) The saturation of the reference field for the Moreland match can be preset to a fixed value. 5) It is important to vary automatically the radiance of the reference field to provide an approximate luminance match as the ratio of primaries in the mixture field is changed. CONCLUSION: These measurements allows us to determine optimal conditions for automated colour vision examinations and to make recommendations for an international standard.

Color Perception Tests↗
PubMed1984

Infant color vision: the effect of test field size on Rayleigh discriminations.

The capacity of 1- and 3-month-old infants to discriminate 589 nm and 650 nm test fields from a 589 nm surround was tested using the forced-choice preferential looking (FPL) technique. The size of the test field ranged from 1 to 8 degrees. Test field size strongly influenced the infants' performance. One-month-olds discriminated 8 and 4 degrees (but not 2 degrees) 650 nm fields from the 589 nm surround; 3-month-olds discriminated 4 and 2 degrees (but not 1 degree) 650 nm fields from the 589 nm surround. The dependence of performance on field size suggests that infants' discrimination failures with small fields are due to immaturities of spatial processing or postreceptoral chromatic mechanisms, rather than to any absence or anomaly of receptor types. In addition, adult subjects rated the hue, brightness, and salience of the test stimuli at 0, 26, 52, and 78 degrees eccentricity. The analogy often made between infant vision and adult peripheral vision is discussed in relation to these data.

Adult↗
PubMed1978

Cat color vision: the effect of stimulus size.

Adult cats were trained to discriminate blue from green and gray. Although the cats could discriminate the intensity of stimuli whose areas ranged from 33 to 0.36 square centimeters they could not discriminate color when the stimulus was 0.36 square centimeter (less than 20 degrees visual angle). This influence of stimulus size may account for both positive and negative results of previous studies.

Animals↗
PubMed1978

Color vision mechanisms in monkey striate cortex: dual-opponent cells with concentric receptive fields.

1. I have recorded with tungsten microelectrodes from single cells in the monkey's visual cortex and have specifically studied those neurons which were sensitive to the color of the stimulus. In the primate striate cortex there are four classes of color-coded cells. The cells described in this paper have concentric receptive fields with one red-green opponent-color system in the field center and the opposite organization in the surround. These dual-opponent cells were nost sensitive to the simultaneous presentation of two different colors, one covering the field center and the other illuminating the surround. They are probable involved in the perception of simultaneous color-contrast phenomena. 2. Spectral sensitivity curves revealed that both the field centers and the surrounds received opposite types of inputs from red-sensitive and green-sensitive cones. None of the cells tested had inputs from rods. 3. Area-sensitivity curves showed that peripheral suppression was present for both phases of the center opponent-color system. The boundary between the center and the surround was the same for both sets of opponent systems. Some cells had "silent" surrounds, which did not respond to annular stimuli. 4. Multiple-unit recordings from a concentric cell and one of its presumed afferents yielded information regarding its possible synaptic inputs. In some cases the cells appeared to receive contacts from red/green opponent-color geniculated fibers with circular receptive fields that lacked an antagonistic surround (similar to Wiesel and Hubel's (37) type II class). In other instances the afferents had on-center, off surround receptive fields or the reverse, but received inputs from only one cone type, either red or green (similar to Wiesel and Hubel's type III class). 5. Concentric cells were always driven by only one eye. 6. The laminar distribution of these cells was limited almost entirely to layer IV and its subdivisions. 7. The cumulative evidence presented in this paper indicates that the concentric cells probably received direct geniculate inputs and, therefore, they are the first cortical stage in the integration of color-contrast information.

Animals↗