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A method is described to assess the precision of eye movement monitors by comparing the difference in two sequentially measured eye positions with the relative positions of afterimages that were induced at the same moments. A 0.1-0.3 min of arc sensitivity could be reached, using a vernier method. The precision of the scleral coil technique was 1 min of arc.
A cellular model of the primate retina has been developed. Unlike existing models, it incorporates spatial non-uniformities, such as the random arrangement of L and M cones, and the radial dilation with eccentricity. Based on a population of ganglion cell activities, colour-image representation is modelled with the luminance and the R-G opponent channels. The developed model reproduces experimentally known properties in temporal and spatial vision. Furthermore, spatio-temporally coupled properties such as transition from positive to negative phases in an afterimage, are recapped. In colour vision, the model can explain the insensitivity in our colour perception to the L/M cone ratio.
Psychophysical research has documented the existence of three processes in light adaptation: a fast subtractive process, a divisive process that is fast at light onset and slower at light offset, and a very slow subtractive process (Hayhoe et al., 1987). In the neural model developed here, the fast subtractive process is identified with horizontal cell feedback onto cones and the divisive process with amacrine cell feedback onto bipolar cells. The very slow subtractive process is identified with the modulatory feedback circuit from amacrines via interplexiform cells to horizontal cells. A nonlinear dynamical model is developed incorporating these aspects of retinal circuitry along with both ON- and OFF-center M and P pathways. This model is shown to account for many aspects of foveal light adaptation, including negative afterimage formation, and to explain a number of the physiological differences between M and P ganglion cells, including their differing contrast-response functions.
Sex differences were investigated in two experiments on visual persistence: the Ganzfeld and the afterimage. Males were found to hold visual sensation longer than females, particularly in the Ganzfeld where there was little overlap of scores. Variability of experience in the Ganzfeld was also greater for males and they commonly reported 'blank-out' effects while females did not. There was further evidence from both experiments that females are more responsive to the long-wave region of the frequency spectrum.
An afterimage method has been used to investigate the relative magnitudes of the nonmotor and motor components of the fusional response to vertical disparity in a complex visual stimulus of diameter 57 degrees consisting of 50 horizontal lines and a square of side 2.5 degrees in the middle. The largest vertical disparity that evoked a stable fusional response was found to be in the range 3-6 degrees, of which the nonmotor component amounted only to 8-15', i.e., 2-10% of the total. At these fusional amplitudes, binocular single vision was already disrupted in the foveola. When the 50 horizontal lines were omitted from the stimulus so that only the central square of side 2.5 degrees remained, the fusional amplitudes decreased by only 25% while the absolute level of the nonmotor components remained the same. The nonmotor components found here are much smaller than those (amounting to about 2 degrees, or 25-40% of the total response) reported recently in the literature.
This study demonstrates that auras can be produced under laboratory conditions and explained by the principles of afterimages and border contrast phenomena.
Afterimages induced by incoherent light sources have been studied as complex visual perceptions for over 200 years; however, individuals who have viewed a coherent source (a laser) on-axis have reported visual experiences unlike those observed for full-field flashes from incoherent sources. In the present study, 10 volunteers viewed all combinations of blue, green, and red laser light and background colors that matched the wavelengths of the laser sources (a total of 9 conditions). The bright focal (50 microm retinal irradiance diameter) 3-sec. exposures (approximately 9 log trolands-40% of the maximum permissible exposure level) given to the volunteers were administered as they performed a simulator tracking task. A 50/50 mirror (a mirror which reflected 50% of the laser beam into the optical pathway while allowing the 50% of the light from the visual scene to pass through the mirror) permitted simultaneous intrabeam viewing of the laser source and the scene. The volunteers were asked to report what they saw immediately after the laser was turned off and 1-min postexposure. The immediate reports indicated that the image they observed was the same color as the laser source and not the complementary color. Also, the images were of ten surrounded by well-defined borders and, regardless of laser's or background's col or, were generally red. One minute following presentation of the laser light the images seen were predominantly purple, dark or no longer present; however, the edge color when present generally appeared red. The immediate appearance of the images was inferred to be neural in nature and not photochemical. These results suggest the properties of the laser source, i.e., coherency, monochromaticity, and the laser's capacity to place an intense beam of light in a small retinal area, all contributed to the unique appearance of the postflash images.
Recent results obtained from recordings of isolated photoreceptor activity and from correlations of this activity with time-dependent changes in the responses of other retinal cells in several vertebrates have made a thorough revision of former theories of visual adaptation necessary. The present paper reviews the current state of research and relates the new discoveries with psychophysical findings in an attempt to explain human light and dark adaptation from the novel starting point. The former conceptions of adaptation have to be replaced with a three-level process consisting of photochemical receptor neural and network adaptation. Several adaptive mechanisms can be discerned at each level. Depending on adaptation conditions, any level of the three can play a dominating role and can also produce afterimages that display the behaviour of the mechanisms working at each level. The total achievement of visual adaptation is an optimized end product of the actions of all the various mechanisms.
The Zwicker tone (ZT) is defined as an auditory negative afterimage, perceived after the presentation of an appropriate inducer. Typically, a notched noise (NN) with a notch width of 1/2 octave induces a ZT with a pitch falling in the frequency range of the notch. The aim of the present study was to find potential neural correlates of the ZT in the primary auditory cortex of ketamine-anesthetized cats. Responses of multiunits were recorded simultaneously with two 8-electrode arrays during 1 s and over 2 s after the presentation of a white noise (WN) and three NNs differing by the width of the notch, namely, 1/3 octave (NN1), 1/2 octave (NN2), and 2/3 octave (NN3). Both firing rate (FR) and peak cross-correlation coefficient (p) were evaluated for time windows of 500 ms. The cortical units were grouped according to whether their characteristic frequency (CF) was inside ("In" neurons) or outside ("Out" neurons) a 1-octave-wide frequency band centered on the notch center frequency. The ratios between the FRs and the rhos for each NN and the WN condition and for each group of neurons were then statistically evaluated. The ratios of FRs were significantly increased during and after the presentation of the NN for the "In" neurons. In contrast, the changes for the t" neurons were small and most often insignificant. The ratios of the p values differed significantly from 1 in the "In-In" and "In-Out" groups during stimulation as well as after it. We also found that the ps of "Out" neurons were dependent on the type of NN. Potentially, a combination of increased p and increased FR might be a neurophysiological correlate of the ZT.
In 1870 Dvorák rejected Helmholtz's eye-movement account of motion aftereffects (MAEs) on the grounds that it was inconsistent with previous reports of nonuniform rotation in MAEs induced with Plateau spirals. Subsequent observations with spirals that were modified to induce both expanding and contracting MAEs simultaneously, together with the use of stationary negative afterimages during induction and test, were offered as further counter-examples to the eye-movement hypothesis. Dvorák's conjectures that perception (and misperception) of movement involves a unitary perceptual dimension of stimulus change also led him to investigate whether aftereffects comparable to MAEs could be induced along other stimulus dimensions in vision (luminance gradients), and in audition (gradients of pitch and intensity). It is suggested that Dvorák's observations, taken as a whole, may be interpreted as an attempt to provide evidence challenging the Helmholtzian traditions underpinning eye-movement accounts of MAEs. The nature and outcomes of these observations are provided in a translation of the original work, and are subsequently discussed in relation to some contemporary empirical counterparts.
To investigate visual afterimage technique as a means of producing retinally stabilized pattern, children's judgments of time-dependent shifts in chromatic appearance of random-dot configurations were twice examined within a 3-wk. interval. 13 subjects, aged 7 to 12 yr., were very consistent (r = .93) in their test-retest response times. This supports the belief that after image procedures can be developed as a reliable means of studying developmental aspects of stabilized pattern perception.
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