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PubMed1984

Visible persistence as a function of spatial frequency, number of cycles and retinal area.

Using a variety of measures it has been shown that processing time increases with increasing spatial frequency. Long and Sakitt (1981) [Vision Res. 21, 1387-1393] investigated duration of visible persistence as a function of both spatial frequency and number of cycles present. They concluded that number of cycles and not spatial frequency is the crucial variable in determining duration of visible persistence. The present paper investigates this issue in three experiments. Experiments 1 and 2 determined duration of visible persistence with spatial frequencies of 2, 4, 8 and 10 c/deg while holding both number of cycles and grating area constant in a dark surround and in a light surround. Stimulus durations of 50 and 300 msec were used in Experiments 1 and 2 respectively. The results at each stimulus duration showed an increase in duration of visible persistence with increasing spatial frequency similar to that found in most previous reports. This increase was less with a 300 than with a 50 msec stimulus duration. Whether the gratings were presented in a light or a dark surround had no significant effect. Experiment 3 showed that at 2 c/deg duration of visible persistence increased with increasing size of the grating stimuli when all stimulus sizes fell within the area of spatial summation. This effect was greater in a dark than in light surround. It is concluded that visible persistence does increase with spatial frequency. Previous results inconsistent with this conclusion are explained in terms of spatial summation.

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PubMed1984

Cancelling of pattern motion: dichoptic and monoptic observations.

Patterns consisting of concentric rings, moving inwards and outwards are superimposed dichoptically and optically. In both conditions opponent patterns motions lead to apparent standstills for considerable periods. In a tentative model both the apparent standstills and the remaining pattern motions are described as by-products, resulting from pattern combinations rather than as direct products of component motions.

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PubMed1984

Optokinetic and vection responses to apparent motion in man.

Apparent motion was investigated as a stimulus for optokinetic nystagmus (OKN) and self-motion perception (vection). Apparent motion was stimulated by stroboscopically illuminating vertical stripes on the interior of a large drum that rotated about the observer at 20, 40 and 60 deg/sec. We determined threshold stroboscopic frequencies (f) for the appearance of smooth continuous apparent motion and measured responses of pursuit, OKN, optokinetic after nystagmus (OKAN) and vection, to stroboscopic frequencies at, above and below f. Pursuit occurred for all of these stimuli. However OKN, OKAN and vection only occurred for frequencies equal to or greater than the threshold for continuous apparent motion. Our results suggest that pursuit can occur as a response to apparent motion generated by both small and large image displacements, while OKN and vection are responses to apparent motion generated by small image displacements only. These results suggest that different afferent sources are utilized for the control of pursuit and of the slow phase of OKN.

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PubMed1985

Brightness reversal in the natural visual environment: a Venetian blind effect.

If a partially open Venetian blind is lighted by the sun, or by diffuse light from the sky, then the upper portion of each slat will be brightly lighted and the lower portion shaded. If an observer moves the head downward while viewing a dark object silhouetted against the sky, then the object displays a reversal of brightness, appearing brighter than the sky while the head is moving downward. Moving the head upward produces no brightness reversal. These observations in the natural visual environment are consistent with earlier laboratory demonstration under several conditions.

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PubMed1985

Visual persistence from brief letters and pictures.

The visual persistence from briefly presented letters and pictures was assessed by the popular probe-matching procedure over a range of background and target luminance levels and for several color conditions. It was determined that the fading visible persistence measured in this way increased with increasing target luminance and with decreasing background luminance. For small foveal presentations, photopically-matched targets of differing wavelength produced equivalent persistences; but for larger, parafoveal presentations, scotopically-matched targets of differing wavelength produced equivalent persistences. This was true for both letter and picture targets. Results were discussed in terms of an early sensory locus to such persistence effects. The strong consistency of these findings to some previous work and the apparent inconsistency with other work were treated in terms of different kinds of visual persistence effects assessed by different experimental methods.

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PubMed1986

Temporal integration in the visual system: influence of temporal dispersion on figure-ground discrimination.

Psychophysical measurements were carried out with a microcomputer-controlled matrix of 32 X 32 light emitting diodes to determine temporal parameters of figure-ground separation processes. The task was to detect a figure that was dispersed in time. Between each two figure elements n noise elements were interspersed. The results of these experiments indicate that the discrimination of figures hidden in dynamic noise is possible even if figure elements are dispersed in time over several hundred milliseconds. The maximal dispersion time still compatible with figure discrimination (Tmax) depends critically on the number n of interspersed noise elements, on the subject's expectancy and on the number of elements used for the generation of the figure. For simple figures such as triangles Tmax could be as long as 1.5 sec when n was 4. Our experimental results suggest that the neuronal representation of the briefly displayed (less than 6 msec) pattern elements outlasts their physical presence by at least 400 msec. This persistence of neuronal representations must occur at a level of processing where retinotopy is still preserved, since the only cue for figure-ground discrimination is the difference in the local density of figure and noise elements.

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PubMed1986

Temporal integration in amblyopic vision.

Amblyopic subjects were tested on different visual tasks which required temporal integration of successively presented stimuli: a figure had to be detected whose components were displayed successively and hidden in spatio-temporal noise. The time interval T over which the figure elements were dispersed was varied and the longest T value still compatible with figure detection was determined. In all subjects these T values were considerably longer for the normal than for the amblyopic eye. A missing square had to be detected in a checker-board of 3 X 3 squares that was presented in two successive frames, each frame containing 4 squares. With the normal eye, identification of the missing square was possible over considerably longer interstimulus intervals (ISIs) than with the amblyopic eye. Changes had to be detected in two patterns of randomly distributed squares that were presented successively with varying ISI whereby one square was added or subtracted in the second pattern. With the normal eye, detection of changes was possible over much longer ISIs than with the amblyopic eye. These experiments show a deficit of the amblyopic visual system to integrate temporally separated stimuli. We conclude that amblyopia is associated with a marked reduction of the duration of visual persistence and suggest that this is due to shortening of normally sustained neuronal responses.

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PubMed1989

McCollough aftereffects in strabismus and amblyopia.

In strabismic people, the functioning of the deviating eye is impaired. This impairment is binocular in origin since it depends on stimulation of the straight eye; sensitivity and acuity of the deviating eye are usually better when the straight eye is patched than when both eyes are viewing. We investigated interactions between the eyes in strabismic people by using the McCollough color aftereffect as an exploratory procedure. Both normal and strabismic people adapted to black and colored bars and then examined black and white test bars. They reported colors in the achromatic test bars that were complementary to the adapting colors; this is the McCollough aftereffect. Both a monocular McCollough effect and a binocular McCollough effect were induced in people having normal vision. Strabismic people did not show a binocular McCollough effect. Aftereffect strengths were the same in each eye of normal people but were stronger in the impaired eye of strabismic people. A speculation is offered as to why the "non-seeing" eye of strabismic people "sees" the aftereffect better.

Adaptation, Ocular↗
PubMed1989

The effects of dichoptic and binocular viewing on bistable motion percepts.

Two competitive percepts are produced from a bistable stroboscopic motion display. In this display two frames, each containing three horizontally arrayed elements are presented alternately for several cycles. At short interstimulus intervals (ISIs) element or end-to-end motion responses are obtained when the two inner, spatially overlapping elements are seen as stationary and the third element moves back and forth from one end to the other end. Group motion responses are obtained at longer ISIs when the three elements are seen to move back and forth as a group. The dominance of these two percepts across ISIs was controlled by the manipulation of (1) element size, (2) frame duration, and (3) viewing conditions. Under both binocular and dichoptic viewing, element motion responses increase as element size and frame duration decrease. By maximizing pattern persistence substantial element motion responses were obtained dichoptically as well as binocularly. Instead of supporting the existence of two separate, low-level and high-level, motion systems, our data suggest that there is a single, high-level mechanism for motion whose output can be modulated by pattern persistence.

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PubMed1989

Optimal displacement in apparent motion.

Measurements are made of the optimal displacement for an abruptly displaced sinewave grating to elicit a motion aftereffect. At a fixed nominal eccentricity of 4 deg, spatial frequencies ranging from 0.2 to 1.2 c/deg are effective in producing an aftereffect. At any given spatial frequency, the optimal displacement is slightly less than one quarter spatial cycle. The range of effective spatial frequencies does not correspond to the range of optimal spatial frequencies reported for neurons in primate Area V1, but does correspond to that for Area V2.

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PubMed1989

Neural motion after-effects in the cat's striate cortex: orientation selectivity.

Single striate cortical neurones were recorded from adult cats, lightly anaesthetized with N2O/O2/halothane. The receptive fields for the dominant eye were subjected to direction-specific adaptation by a square-wave grating of optimal spatial frequency and velocity, drifting continuously in each neurone's preferred direction. Recovery of the neural motion after-effect induced by prior adaptation was assessed with the same grating pattern which now moved alternately in the preferred and opposite directions. In controls the same tests for recovery followed a period of exposure to a uniform field of identical luminance to the adapting grating. Three sets of measurements were made to establish whether the adaptation was orientation- as well as direction-specific. In the first, test grating orientation was maintained constant and optimal for each neurone whilst adapting orientation was systematically varied. In the second, test orientation was varied whilst maintaining adapting orientation constant. In the third set, adapting and test orientations were initially fixed at each neurone's optimum; they were next set, non-optimally to one side of the optimum. Results from the latter configuration were compared with similar tests in which the test grating remained at that non-optimal orientation whilst the orientation of the adapting grating was now altered to a new point on the other flank of each neurone's orientation tuning curve that was matched for strength of adaptation. Thus the degree of adaptation was identical in each case, but zero orientation difference between adapting and test gratings in one case was contrasted with a substantial orientation difference in the other. The results from all three sets of data were unequivocal: in simple neurones, and in standard and intermediate classes of complex neurones, but not in special complex neurones, the sequential effects of adapting gratings on the responses and sensitivity to subsequently presented test gratings were maximal when their orientations were matched and optimal for each neurone, less marked when orientations were matched but non-optimal. In conclusion, adaptation induced by pattern motion was orientation- as well as direction-specific only in standard (length summating) and intermediate complex neurones, and in simple cells; in special complex neurones it was not.

Adaptation, Ocular↗
PubMed1990

The visible persistence of stimuli in stroboscopic motion.

This paper reports an improved paradigm to measure visible persistence. The stimulus is a pair of lines stroboscopically displayed in successive positions moving in opposite directions. The subjects' judgement of simultaneous appearance of all the presented lines is used to estimate visible persistence. This paradigm permitted independent manipulation of spatial and temporal stimulus separations in linear motion. The resulting estimates of visible persistence increase with spatial separation up to 0.24 deg of visual angle and approaches a maximum value at larger spatial separations. The results are consistent with the existence of a hypothetical visual gain mechanism that operates over small retinal distances to effectively decrease persistence duration with decreasing spatial separation.

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PubMed1991

Effects of background illumination on cat horizontal cell responses.

The process of light adaptation in cat horizontal cells was studied by means of intracellular recordings in the optically intact, in situ eye. Response vs intensity profiles were measured using increment- as well as decrement-flashes of "white light" on steady backgrounds. The effects of background illumination in the mesopic and photopic range on both purely rod-driven horizontal cells and mixed rod and cone input horizontal cells were investigated. Increasing the background illumination for mixed-input horizontal cells strongly reduced the contribution from the rod system. The rod aftereffect in the responses to high intensity flashes is totally suppressed at higher background levels. Light adaptation resulted in a sustained hyperpolarization without a substantial effect on the total response range of the response vs intensity curve. At higher background intensities more of the response range is made up of depolarizing responses to decrements of light. Increasing the background illumination also shifted the operating curve to higher intensities. Increment threshold functions, measured with a 3.9 deg diameter test spot on a large background (8.8 deg diameter) showed a linear relation between log threshold intensity and log background intensity with a slope of, on average, 0.64. The response vs intensity curve for the rod horizontal cell typically spanned a narrower intensity range and was displaced toward lower intensities as compared to that for the mixed input horizontal cells. Background illumination greatly reduced the total response range for rod horizontal cells. Increment threshold curves for rod horizontal cells clearly indicated loss in sensitivity due to response compression.

Adaptation, Ocular↗
PubMed1992

Visual persistence of figures defined by relative motion.

In order to measure visual persistence of figures that were solely defined by relative motion (motion-defined figures or motion figures), random-dot kinematograms were used to form stimulus figures in the two-frame, missing element task introduced by Di Lollo, V. (1977 Nature, 257, 241-243). Experiment 1 showed that motion-defined figures persisted for about 130 msec after the termination of the stimulus presentation (i.e. after the dots stopped moving). This was similar to but several tens of milliseconds longer than the visual persistence of figures which were defined by a luminance difference (luminance-defined figures or luminance figures) in the same random-dot pattern. Since motion detectors are not found in the retina or lateral geniculate in primates, our results strongly suggest that visual persistence is not only a retinal phenomenon but also a cortical one. Experiment 2 investigated the possible influence of motion aftereffects on the visual persistence of motion figures. The results showed that coherent movement of the dots over the whole display after the stimulus offset did not reduce the visual persistence of motion figures, suggesting that the source of this persistence is not a motion aftereffect. In Experiment 3, visual persistence for the motion-defined figures was shown to be longer than that for luminance-defined figures independently of the contrast of the stimulus figure as long as the stimuli could be seen clearly enough. This suggests that different mechanisms are involved in the visual persistence of motion-defined and luminance-defined figures.

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PubMed1992

Dynamic noise backgrounds facilitate target fading.

With strict fixation, a small uniform target of medium contrast, placed at 10 deg eccentricity, faded much faster when presented on a dynamic random noise background than on either a static random noise background or a uniform background of the same luminance. Time to first disappearance was between 10 and 16 sec when the background was dynamic, 26 sec when it was static, and 57 sec when it was uniform. Times were shortest for temporal noise frequencies of the background between 3.5 and 15 Hz. These findings are unexpected: the frequent change of pixel contrast at the edge of the target should perceptually enhance the border, make it less susceptible to local adaptation, and prevent fading. Instead, dynamic random noise facilitates, rather than suppresses fading. Three potential mechanisms are discussed: edge perturbation, jerk effect and surround induction.

Adaptation, Ocular↗
PubMed1992

Two movement aftereffects: evidence for luminance- and color-movement pathways.

Two movement aftereffects (MAEs) that bear closely on the issue of visual processing of color and movement have been isolated. Following adaptation with a vertical luminance stimulus a strong MAE occurred with the same stationary test stimulus oriented horizontally and also in a perfectly uniform field. Neither effect occurred following adaptation with a color equiluminance stimulus. These aftereffects have not been reported before. It is concluded that there are at least three pathways for movement, a color, a color-plus-luminance, and a luminance pathway.

Adaptation, Ocular↗
PubMed1993

The inverse intensity effect is not lost with stimuli in apparent motion.

The inverse relationship between the visible persistence of a briefly presented stimulus and its intensity is well established for static displays. However, with non-static displays, this relationship is only partially reported by previous studies. In order to clarify this topic, we investigated the effect of luminance on the visible persistence of a stimulus in apparent motion. Assuming that persistence duration is a normally distributed random variable, we studied whether the mean persistence of a stimulus could be systematically varied by varying its luminance. Our paradigm permits evaluation of this effect without changing the temporal interval between two successive presentations of the stimulus, thus avoiding the potential influence of this latter factor on persistence. Our results show that the inverse intensity effect still occurs at each of the successive locations of a stimulus in apparent motion. In addition, we provide evidence that increasing the spatial separation between the successive presentations, and decreasing the background luminance, result both in longer persistence duration. Altogether, these findings favour the hypothesis that persistence is actively suppressed by inhibitory interactions between adjacent neural zones.

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PubMed1993

An adaptation-induced pop-out in visual search.

The present study demonstrates that an object embedded in an array of identical objects can pop-out. Dependent on the stimuli preceding the search display, local (chromatic) adaptation causes an identical object to pop-out because it appears to have a colour (Expt 1) or brightness (Expt 2) that is slightly different from the colour and brightness of the other objects in the display. Experiment 3 shows that this pop-out even occurs when the stimulus preceding the search display is presented for only 100 msec.

Adaptation, Ocular↗