Measurement of accommodation in dim light and in darkness by means of the Purkinje images.
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After seeing his hand through wedge prisms, a subject points incorrectly with that hand at auditory as well as visual targets. The other hand is virtually unaffected. Thus the change cannot be solely visuo-motor or visual. Other evidence suggests that it is a change in felt hand location, rather than motor learning. When the subject's adapted hand feels as if it is pointing straight ahead, for example, it is actually pointing off to one side.
Prolonged exposure to the chromatic dispersion produced by prism spectacles leads to a perceptual adaptation. The adaptation develops rapidly in the first two days of the wearing of the spectacles, and seems to be a special reac ion to the relative change in illuminance at intensity gradients on the retina.
Reducing the target diameter of an adapting (conditioning) flash of light results in a progressive rise in the conventional light adaptation curve, as measured with a small superimposed test flash presented at the end of adapting flashes of variable duration. When both targets are the same size, an abrupt and marked rise in threshold is obtained, resulting from a unique effect that occurs near the termination of the adapting flash. This effect can be demonstrated by means of a variable delay procedure, and it indicates that neural as well as photo-chemical processes limit the time course of light adaptation.
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Certain ganglion cells from the central region of dark-adapted retina of the rhesus monkey respond to stimulation of both rod and cone receptors. With dim stimuli the function of these ganglion cells is determined entirely by the rods; with brighter stimuli that affect both dark-adapted rods and cones, little evidence of rod function is detectable because a cone mechanism appears to determine both the latency and frequency of ganglion-cell firing.