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C E Sternheim

Publications and source records attributed to C E Sternheim.

At least 19 recordsLinked to original sources

Achromatic and chromatic sensation as a function of color temperature and retinal illuminance.

Changes in color appearance with retinal illuminance were studied by scaling the achromatic, yellow, and blue sensation components for test lights with color temperatures from 3041 to 8650 K at 4.10, 2.18, and 0.33 log Td. At 4.10 log Td two observers showed similar pure whites (4823 and 5258 K) and narrow transition zones (1502 and 969 K) from yellow to blue chromatic response categories. The relative amounts of yellow, blue, and white varied with color temperature in a similar manner for both observers. One observer maintained similar absolute whites and transition zones for all illuminances. For the second observer the transition zone broadened and shifted to higher color temperatures as illuminance decreased. At color temperatures both above and below the transition zone chromatic saturation was greatest at the intermediate illuminance. The loss of saturation at 0.33 and 4.10 log Td is consistent with the observation that as the illuminance of a spectral color is raised above threshold, saturation increases to a maximum and then falls. Our findings reinforce the notion that at relatively low illuminances chromatic responses increase with increasing illuminance more rapidly than achromatic responses and that the opposite is true at high illuminances.

Adult↗

Visual segmentation of a heterochromatic field into center/surround components.

The process of visual segmentation was studied by quantitatively estimating the apparent difference (i.e. the perceptual contrast) between two segments of a heterochromatic field. A chromatic test bar (Munsell 5R 6/6, 5BG 6/6, 5Y 6/6, or 5PB 6/6) was centered in an achromatic surround (Munsell N6) and the luminance contrast between the test bar and surround was varied between 0 and 39%. At equiluminance (0% luminance contrast) the chromatic border between center and surround was vague and perceptual contrast was minimal. When luminance contrast was increased slightly (5-15%) the border between center and surround was more distinct and perceptual contrast was almost two times greater than predicted by a model that combines spatial differences in chromaticity and luminance as orthogonal vectors. A luminance border may enhance perceptual contrast by increasing the salience of the center/surround hue difference. A vector model is consistent with perceptual contrast only at relatively high luminance contrasts, where hue differences play a relatively minor role in visual segmentation.

Color Perception↗

Change in hue of spectral colors by dilution with white light (Abney effect).

Monochromatic light, when mixed with white light, not only becomes desaturated but also changes in hue ( Abney effect). This effect was studied in three observers by using three unique hues (blue, green, and yellow) and four compound (intermediate) hues. The whites used for desaturation ( desaturants ) included Abney 's white (3890 K), two bluish whites (10,000 and 20,000 K), and each observer's own, perceptually neutral white (6200-6980 K). Test stimuli of 0.5 degree diameter were presented to the dark-adapted fovea for 1 sec in a dark surround. Abney 's results were confirmed, except in the shortwave and middle-wave parts of the spectrum. At short wavelengths we always observed a hue shift toward increasing redness, whereas Abney reported a shift toward blue. At middle wave-lengths (500-556 nm), we found smaller effects than did Abney . Here Abney 's white produced an increase in perceived yellow, whereas all other desaturants produced an increase in perceived green. Two colors, blue-green and yellow, changed least. In general, the hue shifts increased with decreasing colorimetric purity (from 1.0 to 0.5). The results are discussed in relation to color additivity, constant-hue loci, and the Benzold -Br ucke effect.

Adult↗

Interaction of receptive field responses and shift-effect in cat retinal and geniculate neurons.

Spike activity of single optic tract fibres and lateral geniculate cells of the lightly anaesthetized immobilized cat were recorded in response to short, small (local) test flashes into the receptive field center before, during and after rapid displacements of a remote, large (global) pattern. 2. The majority of retinal and geniculate neurons failed to produce algebraic summation of the excitatory shift-effect and an excitatory test response. 3. For many cells outside lamina A and A1 of the dorsal lateral geniculate body the test response was smaller than the control even though two excitatory responses were combined. 4. The resonses to displacements of a steady, local spot are weakly affected by simultaneous displacements of a global pattern if the local responses are strong; but if the latter are weak the global shift-effect dominates the response to a displacement of the total pattern. 5. Saccadic suppression may be explained by retinal and geniculate neurons functioning in two modes of local or global responses, both of which cannot be transmitted properly at the same time.

Animals↗