Dark adaptation in perimetrically blind fields.
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Using the electroretinogram as the criterion of retinal activity the flicker fusion frequency, course of dark adaptation, and spectral sensitivity of the pure cone retina of the diurnal gecko, Phelsuma inunguis, were investigated. Both the curve relating flicker fusion frequency to stimulus intensity and that relating the amplitude of the flicker response to stimulus intensity showed a break as the intensity was increased. The dark adaptation curve was that typical of cone retinae; there was no break, adaptation was relatively rapid, and there was a total increase of sensitivity of only about 3 log units. The spectral sensitivity curve showed two maxima, a major one at about 560 mmicro and another at about 460 mmicro. Chromatic adaptation with red and blue lights demonstrated the presence of two independent mechanisms. Although red adaptation could not have had a direct effect on the pigment responsible for the "blue" mechanism the sensitivity of this mechanism was depressed by red adaptation. The possible relationships of the two mechanisms are discussed.
Characteristics of the electroretinogram (ERG) produced by the essentially all rod eye of the rat are presented as functions of the number of quanta absorbed by each rod per stimulus flash. The ERG's were obtained with 1.5 msec. stimulus flashes and uniform illumination of the entire retina. Under these conditions, distortions in the ERG due to stray light are minimized, and the ERG more accurately reflects the activity of its retinal sources. The effects of background light and two forms of dark adaptation were studied and compared. The results, especially for the b-wave, permit an interpretation in terms of two distinct processes. One process appears to determine the b-wave latency. This process is almost independent of the state of adaptation of the retina. The other process does not affect the latency, but determines the b-wave threshold and amplitude. This process strongly depends upon the state of adaptation. Moreover, the effects of dark adaptation on this amplitude-determining process are almost identical with the effects of background light.
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