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W A Rushton

Publications and source records attributed to W A Rushton.

10 recordsLinked to original sources
PubMed1977

Visual adaptation.

1) The eye may be regarded as an automatic camera that keeps the average sensitivity near the middle of the working range. 2) Nerve signals are contrast-coded, and hence are not changed by changes in general illumination. 3) Rod thresholds can be raised three-fold by a background from which only 1% of the rods have caught one quantum. 4) Adaptation is of two kinds a) to backgrounds (the Weber-Fechner relation) and b) to bleachings which is entirely different. 5) After bleaching the threshold is raised as though a bright background were present. The positive after-image following bleaching has quantitatively the properties of that bright background. 6) The visual incapacity after bleaching seems a pointless visual disaster.

Adaptation, Physiological↗
PubMed1977

Obituary.

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Bibliographies as Topic↗
PubMed1976

Isolation of rod and cone contributions to cat ganglion cells by a method of light exchange.

1. The great majority of cat retinal ganglion cells are known to receive signals from rods and from a single (green) cone type. The centre region of the receptive fields of these cells was stimulated by a spot that changed back and forth from orange to white. By adjusting the intensity of the white spot relative to that of the orange a condition could be established at which the photon-catch rate of the rods remained unchanged during the orange-white exchange. At this intensity setting, termed the rod isolept, rods are thus unstimulated by the exchange, however intense, and the ganglion-cell response was found to be due entirely to the green cones. At another intensity setting of the white spot relative to the orange (cone isolept), the photon catch of the green cones remained unchanged during the exchange and ganglion-cell responses were found to arise entirely from the rods. 2. A neutral wedge in the combined exchange beam (but not in the steady background that covered the whole receptive field) regulated the size of the exchange stimulus and thus the magnitude of the ganglion-cell discharge heard from a loud speaker to the exchange. Exchange threshold was the wedge setting at which this change in firing rate could only just be heard. 3. At the cone isolept, cones remain unstimulated however intense the exchange stimulus, and the rod increment threshold curve was determined over its full range from absolute threshold up to saturation. Likewise, at the rod isolept, the cone increment threshold curve was determined over the same intensity range as for the rods. Rod saturation was found to occur at the point where the cone increment threshold curve began to rise from its absolute threshold level toward its Weber region. 4. The exchange approach also enabled both rod and cone dark-adaptation curves following a strong bleaching exposure to be obtained in the same experiment by moving successively between the cone and rod isolepts. At the cone isolept the time course of early rod dark adaptation could thus be determined when the rod threshold to flashing spots lay well above that of the cones.

Animals↗
PubMed1976

Cancellation of rod signals by cones, and cone signals by rods in the cat retina.

1. The interaction of rod and cone signals at the level of cat retinal ganglion cells was studied by a method of light exchange. Two spectrally distinct lights were exchanged in such a manner that the rate of photon catch by rods increased in a stepwise manner at the same moment that the cone rate decreased in the same manner, and vice versa. 2. Under any conditions of adaptation, where both rods and cones contributed to the ganglion-cell discharge, it was always possible to adjust the ratio of the magnitudes of the rod and cone stimuli so that no change in ganglion-cell discharge could be detected by listening to the recorded activity via a loudspeaker. We term this condition a silent exchange. 3. On the face of it, the condition of silent exchange arises when rod and cone signals are able to cancel one another, when made opposite in phase by the exchange situation. But was this silence due to a true cancellation of the signals from one photoreceptor type by those of the other type, or was it due to our failure to stimulate the photoreceptors adequately? In order to test whether rod signals can cancel those of cones we bleached both visual pigments and set our exchange apparatus to stimulate the two photoreceptors in the antagonistic manner described above. At first no response could be heard on exchange, for the thresholds of both rods and cones lay above that of our apparatus. But the cones soon recovered and a strong response was heard on exchange. With no change in our stimulating situation, this response diminished with time and silence was again restored. This restoration of silence could not be due to the cones alone, for with time their sensitivity could only further increase. It could only be the increasing sensitivity of the rods that quietened the cone signals. In agreement with this conculsion, the dark-adaptation curve of the rods showed that they became sensitive to our stimulus at the time that the cones began to be silenced. 4. By means of coloured backgrounds we have also shown the converse, namely that rods signals can be cancelled by those of cones.

Animals↗
PubMed1976

The dark adaptation curve of rods measured by their after-image.

1. The common dark adaptation curve exhibits two branches; the course of the rod branch cannot normally be measured at early times since it lies above the observed cone thresholds. In this paper we measure it. 2. this is done by observing the negative after-image against a uniform background critically adjusted in luminance. 3. adjacent to the bleached area to be studied is a second area more strongly bleached. If the background intensity is below threshold for the less bleached area it will not be seen there; but if the background is above that threshold, this area will be seen brighter than the other. 4. the dark adapted threshold on the less bleached area is therefore the background luminance which just permits the two areas to be distinguished in the after-image. 5. after 5 min cones have quite recovered, and thus have no after-image to contaminate the rod image. 6. the rod curve measured by after-image is traced over 5 units of log threshold: it is an exponential with half life of 4.5 min, and coincides with the time course of regeneration of rhodopsin in man.

Afterimage↗