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Biomedical subjects

K Nordby

Publications and source records attributed to K Nordby.

29 records · Page 2Linked to original sources
PubMed1988

Spatial vision of the achromat: spatial frequency and orientation-specific adaptation.

1. The psychophysical technique of selective adaptation to stationary sine-wave gratings of varying spatial frequency and orientation was used to investigate the central processing of spatial information in the visual system of the complete achromat. 2. For adapting spatial frequencies of 1 and 2 cycles/deg, the spatial frequency and orientation selectivity of contrast threshold elevation is similar for achromatic and trichromatic vision. 3. For adapting frequencies below 1 cycle/deg, the achromat shows threshold elevations of normal magnitude with symmetrical spatial frequency and orientation tuning for adapting frequencies as low as 0.09 cycles/deg with 'bandwidth' estimates similar to those found at high frequencies in the trichromat. Below 0.66 cycles/deg no after-effect could be obtained in the trichromat, and the frequency tuning at 0.66 cycles/deg was skewed towards higher frequencies. 4. The interocular transfer of low-frequency adaptation in the achromat was 50%, which is the same value obtained at higher frequencies. 5. The time course of the decay of low spatial frequency adaptation in the achromat was similar to that found at higher frequencies. 6. Control experiments show no low-frequency adaptation in peripheral vision or in central vision in the dark-adapted trichromat indicating that low spatial frequency adaptation cannot be elicited through the rod system of the trichromat. 7. It is proposed that the observed range shift of adaptable spatial frequency mechanisms in the achromat's visual cortex is the result of an arrest at an early stage of sensory development. The visual cortex of the achromat is comparable, with respect to spatial processing, to that of the young, visually normal human infant.

Adaptation, Ocular↗
PubMed1988

The directional sensitivity of the photoreceptors in the human achromat.

1. The anatomical nature of the retinal photoreceptors in a typical, complete achromat was investigated by measuring their directional sensitivity. 2. A small (0.5 deg), brief (94 ms) test flash was placed at threshold by varying either its intensity (indirect method) or the intensity of a large (5 deg) adapting field (direct method). The dependent variable was the intensity of light required for the detection threshold as a function of the position of entry in the pupil. An infra-red viewing system was used to monitor the achromat's pupil and eye position. 3. At both scotopic and mesopic adapting field luminances, the complete achromat's receptors displayed only a small directional sensitivity effect. The effect was not wavelength dependent and could be attributed solely to the rods. 4. The results are consistent with other psychophysical evidence indicating that the complete achromat's retinae lack the post-receptoral function of the cone photoreceptors. Therefore they do not confirm previous reports that complete achromats have a second, high-intensity type of photoreceptor.

Color Vision Defects↗
PubMed1987

Regional variation of contrast sensitivity across the retina of the achromat: sensitivity of human rod vision.

1. Detection thresholds for two-dimensional Gabor functions of varying spatial and temporal frequency were used to investigate the post-receptoral sensitivity across the retina of the typical and complete achromat. 2. Under photopic conditions there is no evidence for post-receptoral cone function at any retinal eccentricity investigated. Sensitivity saturates in a way consistent with known psychophysical and electrophysiological measures of rod saturation. This occurs in a unitary fashion across the retina. 3. Under scotopic conditions the regional fall-off in spatio-temporal sensitivity is similar for the achromat and duplex retina. This suggests that the rods in the achromat make normal neural connections. 4. Taken together this supports the contention that the typical and complete achromat is a functional rod monochromat and hence can be used to explore the sensitivity of the isolated rod post-receptoral mechanism under mesopic conditions where its sensitivity is optimal. This is where its contribution is most difficult to isolate in the duplex retina. 5. For the human rod mechanism, mesopic post-receptoral sensitivity for all spatio-temporal stimuli is optimal in the central region of the retina and falls off as a function of eccentricity. 6. For localized stimuli, peripheral spatial sensitivity is reduced evenly at all spatial frequencies compared with that of the central retina. A similar displacement of the spatial sensitivity function of the rod mechanism occurs as illuminance is reduced. 7. For localized stimuli, temporal acuity of the rod mechanism is around 20-25 Hz irrespective of retinal position. As the illuminance is further lowered dynamics of the rod pathway are reduced irrespective of retinal position and the sensitivity function maintains a bandpass shape. 8. The regional distribution sensitivity of the rod mechanism changes as illuminance is reduced from mesopic to scotopic levels.

Color Vision Defects↗
PubMed1986

Spatial and temporal limits of vision in the achromat.

Threshold detection for sine-wave grating stimuli of varying spatial and temporal frequency was used to investigate the nature of spatial and temporal post-receptoral sensitivity in the typical, complete achromat. Threshold spatial and temporal sensitivities under low photopic conditions show no evidence of cone function. The abrupt fall-off in sensitivity is consistent with known psychophysical and electrophysiological measures of rod saturation. Threshold spatial and temporal sensitivities under scotopic conditions are identical in form and absolute sensitivity to that of the normal scotopic system. Spatial and temporal acuity measurements substantiate the above conclusions based on contrast sensitivity. We conclude that the typical and complete achromat possesses only a normal functioning rod post-receptoral mechanism.

Color Vision Defects↗
PubMed1986

Spatial and temporal properties of human rod vision in the achromat.

The spatial and temporal properties of rod vision were measured for stimuli at and above the detection threshold in an achromat whose spectral sensitivity, dark adaptation, spatial and temporal thresholds and Stiles-Crawford effect suggest the presence of only a normally functioning rod system. The properties of rod and cone vision were compared at illuminances where their respective sensitivities were optimum. The threshold spatial sensitivity of the rod mechanism under optimum illumination (180 scotopic trolands) exhibits bandpass properties with a peak sensitivity of around 80 at 0.5 cycles/deg and a spatial acuity of 6-7 cycles/deg. The threshold temporal sensitivity also exhibits bandpass properties under these conditions with a peak sensitivity of around 80 at 5 Hz and a temporal acuity of 30 Hz. For stimuli of low spatial frequency (less than 0.3 cycles/deg) and low temporal frequency, the threshold sensitivities of rod- and cone-mediated vision are identical. Rod- and cone-mediated vision display comparable spatial and temporal discrimination for targets of equal suprathreshold contrast over the low to mid spatial and temporal range that they share. Rod-mediated discriminations fall below those of cone vision above 1 cycle/deg for spatial judgements and above 15 Hz for temporal judgements. The number of discriminable steps in spatial frequency and temporal frequency at threshold is similar for rod and cone vision over the spatio-temporal frequency range that they share. Over this range rod- and cone-mediated vision can discriminate four steps in spatial frequency and one step in temporal frequency. These results suggest that rod vision shows comparable spatio-temporal discrimination performance to cone vision and that it is subserved by at least five spatial and two temporal labelled detectors. The response of the highest spatial frequency filter subserving rod vision extends from 0.5 to 6 cycles/deg.

Color Vision Defects↗
PubMed1984

Dark-adaptation of the human rod system.

Following substantial bleaching, dark-adaptation thresholds of a complete rod monochromat and of a subject with normal colour vision were measured using a Wright colorimeter. When precautions were taken to ensure that the fixation point fell on the same retinal area during the threshold measurements as during the bleaching period, the dark-adaptation threshold curves of the rod monochromat followed exactly the same course as those of the normal subject subsequent to the cone-rod break of the long-term, normal dark-adaptation curve; irrespective of the intensity and the duration of the bleaching and the wavelength of the test stimulation. In contrast to the normal subject, however, the dark-adaptation curves of the rod monochromat showed no evidence of any cone function at photopic intensities. Furthermore, as opposed to previous measurements which show a simple linear relationship between fraction of bleached rhodopsin and log threshold, the present results show that there is a close linearity between log fraction of bleached rhodopsin and log threshold. This linear relationship is obtained despite varying extents of bleaching and subsequent dark-adaptation periods.

Adaptation, Ocular↗
PubMed1981

Photopic and scotopic flicker sensitivity of a rod monochromat.

The sensitivity to sine-wave flicker of a rod monochromat was compared with that of a normal subject at photopic and scotopic levels of luminance. The sensitivity of the rod monochromat in the low-frequency region (below 3 Hz at scotopic levels and below 12 to 14 Hz at photopic levels) was found to be superior to that of the control. This superiority was most pronounced at photopic levels, where the rod monochromat frequently showed a two-peak sensitivity curve.

Adult↗
PubMed1980

Rod monochromat sensitivity to sine wave flicker at luminances saturating the rods.

The flicker sensitivity (temporal modulation transfer function) of a rod monochromat was measured at luminances in the range of 8 to 782 scotopic td. The results could be fitted by a single curve shifted vertically, suggesting that rod saturation is independent of the temporal properties of the stimulus. This is consistent with the hypothesis that rod saturation is a pure receptor phenomenon.

Adult↗
PubMedDate not supplied

Two signals in the human rod visual system: a model based on electrophysiological data.

In the human rod visual system, self-cancellation of flicker signals is observed at high rod intensity levels near 15 Hz, both perceptually and in the electroetinogram (ERG). This and other evidence suggests that two rod signals are transmitted through the human retina with different speeds of transmission. Here we report a series of flicker ERG recordings from a normal observer and an observer who lacks cone vision. From these results, we propose a quantitative model of the two rod signals, which assumes (1) that the amplitude of the slow signal grows linearly with log intensity but then saturates at approximately 1 scot. td; (2) that the amplitude of the fast signal grows linearly with intensity; (3) that there is a difference in time delay of approximately 33 ms between two rod signals of the same polarity (or of approximately 67 ms if the signals are of inverted polarity); and (4) that the time delay of both signals declines linearly with log intensity (by approximately 10 ms per log scot. td). These simple assumptions provide a remarkably good account of the experimental data. Our results and model are relevant to current anatomical theories of the mammalian rod visual system. We speculate that the slower signal in the human ERG may reflect the transmission of the rod response via the rod bipolars and the AII amacrine cells, while the faster signal may reflect its transmission via the rod-cone gap junctions and the cone bipolars. There are, however, several objections to this simple correspondence.

Adult↗