Biomedical subjects

S Anstis

Publications and source records attributed to S Anstis.

At least 19 recordsLinked to original sources

PubMed1999

Spatial distortions in rotating radial figures.

A white sector on a black rotating disk appears spatially compressed. We found that apparent shrinkage: (1) for sectors ranging from 15 to 150 degrees and rotating at 1.25 rps varied in an inverted U-shaped manner from 3 to 16 degrees and back to 11 degrees (corresponding to 20, 16, and 7.5%, respectively); (2) increased with speed of rotation producing maximal compressions of between 7 and 30 degrees for velocities ranging from 0.8 to 2 rps; and (3) affected the leading and the trailing portions of the rotating sector equally, while allowing for apparent expansion of the middle region. Consistent with these findings we found that (4) two black lines 20 mm apart across the center of the rotating disk and extending outward towards the edge appeared to converge when they were actually parallel and were seen as parallel when their end points were physically diverged by 6 degrees. Our findings suggest a foreshortening process which ensures that the shapes of moving stimuli are perceived approximately correctly, irrespective of whether they are actually sharp or blurred.

Adult↗

PubMed1999

Demonstrating the temporal modulation transfer function.

A 120-frame movie, which can be downloaded from specified web sites, allows an observer to see the qualitative form of his or her temporal modulation transfer function. Results collected from two of the authors are presented.

Contrast Sensitivity↗

PubMed1998

Optomotor test for wavelength sensitivity in guppyfish (Poecilia reticulata).

Wavelength sensitivity was measured in the guppyfish by means of optomotor responses to a special apparent-motion display. A set of red and green bars appeared to humans to move to the left if red was darker than green, but to the right if red was lighter than green. At equiluminance there was no apparent motion. By noting the direction in which the fish swam to follow the stripes we were able to record equiluminance points for red, green and blue. Store-bought guppies (Poecilia reticulata) were mildly protan compared with humans, and wild-strain guppies were strongly protan, being 50% more sensitive to short wavelengths and 67% more sensitive to medium wavelengths than human observers. We also measured optomotor responses to achromatic Michelson contrast: responses were maximum if the contrast exceeded 0.3. Finally, the optomotor threshold (signal/noise ratio) for motion coherence was 20% for fine dots and 40% for coarse dots. These stimuli should be easy to use on any non-verbal species.

Animals↗

PubMed1998

Nonlinear combination of luminance excursions during flicker, simultaneous contrast, afterimages and binocular fusion.

The changes in apparent brightness or color, induced into a test spot by a surround, can be greatly enhanced either by flickering the test spot between two luminances, or by binocularly fusing a pair of test spots of different luminances. Simultaneous contrast, in which a white surround makes a grey spot look darker, is greatly enhanced if the spot (not the surround) flickers between black and white. Colour contrast is likewise enhanced by chromatic flicker: on a blue surround, a grey spot looks slightly yellowish, but a yellow/blue flickering spot looks strongly yellow. Temporal successive contrasts, or negative afterimages, are also enhanced by flickering the test field. The negative afterimage of a half-white, half-black rectangle looked dark grey and light grey when projected on a grey test field, but it looked almost black and almost white when projected on a test field that flickered between black and white. Coloured negative afterimages were also enhanced by projecting them on a chromatic flickering test field. We examined the combination rules for pairs of luminances which were presented either successively as flicker or else dichoptically (and fused binocularly). The brightness averaging functions for spatial increments (light spots) on dark surrounds were quasi-linear for binocular fusion but quadratic for flicker. For spatial decrements (dark spots) on white surrounds, the brightness averaging functions were strongly nonlinear winner-take-all for both binocular fusion and flicker. We also found temporal analogues of Fechner's [(1860). Elements of psychophysics. New York: Holt, Rinehart, Winston, 1966] paradox and Levelt's [(1965). British Journal of Psychology, 56, 1-13] dichoptic contour effect. We conclude that the visual rules for combining luminance excursions, whether in flicker or binocular fusion, favour disproportionately the spot with the higher contrast.

Afterimage↗

PubMed1998

Picturing peripheral acuity.

The grain of the retina becomes progressively coarser from the fovea to the periphery. This is caused by the decreasing number of retinal receptive fields and decreasing amount of cortex devoted to each degree of visual field (= cortical magnification factor) as one goes into the periphery. We simulate this with a picture that is progressively blurred towards its edges; when strictly fixated at its centre looks equally sharp all over.

Humans↗

PubMed1997

Reversed visual motion and self-sustaining eye oscillations.

A random-dot field undergoing counterphase flicker paradoxically appears to move in the same direction as head and eye movements, i.e. opposite to the optic-flow field. The effect is robust and occurs over a wide range of flicker rates and pixel sizes. The phenomenon can be explained by reversed phi motion caused by apparent pixel movement between successive retinal images. The reversed motion provides a positive feedback control of the display, whereas under normal conditions retinal signals provide a negative feedback. This altered polarity invokes self-sustaining eye movements akin to involuntary optokinetic nystagmus.

Eye Movements↗

PubMed1996

Adaptation to peripheral flicker.

UNLABELLED: With strict fixation, a flickering disk presented in the peripheral retina rapidly appeared to lose contrast and stop flickering, owing to adaptation. Subjects measured this adaptation by continually adjusting the flicker amplitude of a peripherally viewed disk to hold it just at threshold. RESULTS: (1) The contrast threshold for flicker increased logarithmically over time. (2) The slope of the temporal decay function increased with eccentricity (1-16 deg) and with decreasing disk size (8 deg-3.6 min arc). (3) M-scaling the stimulus size could abolish the dependence upon eccentricity for small disks, but not completely for large disks. (4) The temporal decay rate increased with flicker rate (3-15 Hz), as though each cycle of flicker elevated contrast threshold equally.

Adaptation, Ocular↗

PubMed1995

Aftereffects from jogging.

After running on a treadmill, runners who attempted to jog in place on solid ground inadvertently jogged forwards. One-legged hopping on the treadmill produced an aftereffect in the same leg, but not in the other leg. This non-transfer suggests a peripheral neural site. Judgments of velocity and slope were affected; running on a backward-moving treadmill made a stationary test treadmill seem to move forwards, and running on an uphill-sloping treadmill made a horizontal test treadmill seem to slope downhill. These aftereffects suggest an automatic gain control process.

Adaptation, Physiological↗

PubMed1995

Second-order texture contrast resolves ambiguous apparent motion.

When a black and a white square on a grey surround exchange places, it was previously shown that on a dark surround it is the white square, and on a light surround it is the black square, that is seen in apparent motion (AM). Thus the higher-contrast square carries the AM. We now show that the same is true for second-order AM of texture-defined squares. Squares were defined by four different textures: by anisotropy (horizontal versus vertical random dashes), by alpha numeric letters, by hash marks, or by dot size. The result was that the square that differed more from the surround in texture properties carried the second-order AM. Judgments of texture salience revealed a high correlation between salience and apparent motion. In a third experiment, crossover AM between dissimilar textures was investigated, and it was found that the more salient textures carried the AM. Results cannot be explained by the concept of "texture activity', but instead indicate that the system extracts a measure of "texture contrast' prior to analysis of salience and apparent motion.

Anisotropy↗

PubMed1993

Properties of the visual channels that underlie adaptation to gradual change of luminance.

Following adaptation to a spatially uniform patch of light that is gradually brightening (or dimming), a steady test patch appears to be gradually dimming (or brightening). We measured this ramp aftereffect with a nulling method, as a function of the amplitude and temporal repetition rate of the adapting sawtooth waveform and at various retinal eccentricities and levels of dark adaptation. We conclude that the underlying visual channels respond best to large-amplitude sweeps in luminance of at least 20 dB (1 log unit); but they are fairly insensitive to the temporal rate of this sweep. The channels are present out to an eccentricity of at least 40 degrees but they almost disappear during dark adaptation. The ramp aftereffects were asymmetrical: the subjectively darkening aftereffect produced by a brightening adapting ramp was slightly stronger than vice versa.

Adaptation, Ocular↗

PubMed1991

The contribution of color to motion in normal and color-deficient observers.

By opposing drifting luminance and color gratings, we have measured the "equivalent luminance contrast" of color, the contribution that color makes to motion. We found that this equivalent contrast was highest (greater than 10%) for low spatial and temporal frequencies and was higher for red/green than for blue/yellow stimuli. Equivalent luminance contrast was about 4% for a green/purple stimulus that fell along the tritan confusion line, indicating a modest input to the motion pathway from the short wavelength-sensitive cones (B-cones). Contrast thresholds for the discrimination of the direction of motion showed that the contribution of color to motion was about the same (within a factor of 2) as that for luminance in terms of multiples of threshold contrast. These responses to moving, chromatic gratings could be mediated by any of several factors that can create a residual response in a luminance pathway: temporal phase lag between the responses to the colors of the stimuli, second harmonic distortion in the response and variability in equiluminance points across units. Each of these factors was evaluated experimentally and their combined effect could account for only a small portion of the contribution of color to motion. As a result, we attribute the perception of the motion of equiluminous stimuli to an opponent-color input to directionally selective cortical units. Chromatic stimuli had little or no equivalent contrast for color-deficient observers, whether the stimulus was red/green, which they discriminate less well than normals, or blue/yellow, which they discriminate almost as well as normals. The equivalent contrast measure provided an excellent basis for classifying normal, protan and deutan observers.

Color↗

PubMed1991

The spacing illusion: a spatial aperture problem?

A geometrical illusion in which the horizontal spacing between adjacent parallel lines in a row is underestimated when the lines are tilted away from vertical in a chevron configuration was investigated in two experiments. The perceived spacing was found to decrease as the tilt angle increased, consistent with the idea that separation judgements are influenced by the normal spacing between lines ie at right angles to the line orientation. It is proposed that this illusion reveals an analogue in spatial perception to the well-known aperture problem in motion perception. In establishing the separation of nearby or overlapping shapes in an image, the visual system cannot only rely upon the normal separation of contours belonging to each shape (as would be visible through small spatial apertures or receptive fields), since this varies with contour orientation. The system is therefore faced with a spatial aperture problem. The spacing illusion may arise because information usually available to solve the problem is absent in the illusion figure, or it may reflect a bias in favour of the orthogonal, which is adopted in the face of the ambiguity.

Adult↗

PubMed1990

Motion aftereffects from a motionless stimulus.

Dimming or brightening regions superimposed, slightly out of register, on static light or dark blobs, give rise to apparent motion. When these regions are replaced by apparent brightening or dimming produced by ramp aftereffects, a directional motion aftereffect is perceived. It is concluded that filters sensitive to temporal derivative signals of net brightening or dimming provide an input into the motion pathways.

Attention↗

PubMed1989

The less you see it, the faster it moves: shortening the "on-time" speeds up apparent motion.

The apparent motion (AM) created by two spots illuminated in alteration looks faster when there is dark temporal interval (ISI) between the offset of one spot and the onset of the other than when the spots are presented immediately after one another (no ISI), even though the temporal frequency and the spatial separation between spots are held constant. AMISI looks 18.6% faster than AMnoISI at temporal frequencies between 1.5 and 4.5 Hz. Reducing the duty cycle from 0.5 to 0.05 increases the apparent speedup to 30%. This difference in subjective speed is not due to differential saturation of velocity detectors, nor to the apparent spatial separation between spots, nor to differences in the time-averaged luminance of the stimuli. It is the "on-time", the time for which the spot is visible in one position, that determines the subjective speed. The longer the on-time, the slower the spot appears to move.

Female↗

PubMed1989

A new test of luminous efficiency for babies.

We used the minimum motion method devised by Anstis and Cavanagh (1983) to measure the luminous efficiency of red and green and of yellow and blue for "normal" 1- 3-month-old babies and for one 3-month-old boy destined to be color-deficient because of a deutan mother. Subjects watched a display which created apparent motion, the direction of which depended on the relative luminance of the colors. To determine the equiluminant points, we observed the optokinetic nystagmus elicited by the display as the relative luminance of the colors was varied. The equiluminant points of the normal mothers and their infants were similar to each other but different from those of the deutan mother and her son. Our new method demonstrates the early maturation of input from red and green cones into achromatic pathways. It can also be used to identify some color-deficient infants.

Color Perception↗

PubMed1987

Visual inertia in apparent motion.

Four dots in an imaginary diamond were flashed in succession to give ambiguous apparent motion (AM). The top and bottom dots were flashed at time t1 and replaced by the left and right dots at time t2. If two priming dots were flashed beforehand at time t0 in line with two parallel sides of the diamond, AM was seen along those sides. We call this "visual inertia". The amount of visual inertia (measured by a null method) fell off with increasing angle between the priming dot and the side of the diamond. Visual inertia was still seen when the priming dots were presented to one eye and the test dots to the other, so the effect must be partly central. The timing and length of the priming path made little difference to visual inertia. However, static priming dots were ineffective. We conclude that the visual system was examining at least three successive time frames in deciding which items in one frame correspond with which items in succeeding frames.

Humans↗

PubMed1987

Magnification factor for adaptation of a visual transient mechanism.

After adaptation by an observer to a patch of gradually increasing (or decreasing) luminance, a steady test patch appeared to be gradually dimming (or brightening). These aftereffects did not transfer interocularly. Adaptation to a checkerboard, in which the white squares gradually dimmed while the black squares gradually brightened, gave an aftereffect that was a pattern of intersecting diagonal lines, that is, an extremely blurred checkerboard. The larger the squares of the checkerboard were, the farther into the periphery the aftereffect extended, because small squares were blurred out by the summation areas of the underlying visual channels, which were larger at increasing eccentricities and had diameters of 20 times the resolvable dot separation. The estimated visual acuity of these channels was as low as 20/400. These estimates were confirmed by manipulating separately the local and space-averaged luminances of the adapting stimulus.

Acclimatization↗

PubMed1986

Entrained path deflection in apparent motion.

A dot jumping back and forth between two positions would normally appear to jump along a straight line. But when surrounded by dots which jumped through three positions arranged in a V, it also appeared to jump along a V-shaped trajectory.

Eye Movements↗