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Biomedical subjects

R J Snowden

Publications and source records attributed to R J Snowden.

At least 19 recordsLinked to original sources

Textured backgrounds alter perceived speed.

Both the luminance contrast of an object, and the nature of the background texture over which it moves, are known to influence its perceived speed. In this study the effect of object contrast upon perceived speed was investigated for targets moving across textured patterns of various contrasts. Experiment 1 showed a strong effect of contrast for objects moving over homogenous backgrounds, that was reduced or abolished if the object moved over a textured background. A further experiment suggested that this reduction may be the result of an increase in target visibility, perhaps as a result of additional 'second order' motion signals produced by motion over texture backgrounds. A final experiment suggested that two processes were occurring: (1) higher contrast backgrounds appeared to increase the perceived speeds of all objects; and (2) that higher contrast backgrounds eliminated the contrast induced changes in perceived speed.

Contrast Sensitivity↗

Attention to overlapping objects: detection and discrimination of luminance changes.

Selective attention to 1 of 2 overlapping objects was assessed in a cuing paradigm. Participants detected or identified targets that appeared in 1 of 6 possible target locations (3 on each object). Significant cuing effects for the simple detection of such targets using both reaction time and sensitivity measures of performance were found. Cuing effects were consistently greater when the participants were required to identify some aspect of the target even when the tasks (detection vs. identification) were equated for overall performance level. These differences in cuing effects between tasks were much reduced if the target locations were no longer grouped into 2 objects. It is suggested that identical stimuli can elicit differing attentional mechanisms depending on task type (rather than task difficulty) and that these mechanisms differ in the nature of the representation of the visual world.

Adult↗

Visual perception: here's mud in your mind's eye.

We appear to be unaware of large changes in our visual scene if our attention is temporarily diverted. This suggests that the rich, complete visual scene that we appear to have may be just an illusion.

Animals↗

Colour and polarity contributions to global motion perception.

The influence of the image segmentation cues based on colour and polarity on a motion coherence task were examined. In line with previous reports, when the signal and noise were given unique identities thresholds were much lower than when they were the same, suggesting a strong influence of segmentation. In another paradigm extra noise elements that differed in colour or polarity interfered despite this perceptual segmentation. We suggest that the results when signal and noise have unique identities are attributable to the subjects' ability to attend to a particular location(s) in space. When this strategy was eliminated by presenting the stimuli in the near-periphery or very briefly the effect of the colour or polarity information disappears.

Color Perception↗

The effect of contrast upon perceived speed: a general phenomenon?

The perceived speed of a grating pattern has often been reported to slow as the contrast of the pattern is reduced (though there are some contradictory reports). The mechanism of this perceived slowing has not yet been established nor have the conditions under which the effect occurs (or does not occur). We have therefore examined a range of stimuli that differ upon such aspects as one versus two dimensions, periodic versus nonperiodic, and whether the stimuli occur within a static window. We have also examined a range of stimulus speeds, different types of motion, and simultaneous versus successive presentations. We have found evidence for contrast-induced changes in perceived speed in all our stimuli, and thus suggest that none of the stimulus factors listed above is critical in producing the effect. Though the pattern of results is complex and shows substantial intersubject variation, we generally found that slowly moving patterns presented simultaneously produced the greatest decrease in perceived speed with decreasing contrast. On the other hand faster speeds and successive presentation produced more veridical matches or even an increase in perceived speed with decreasing contrast.

Computer Graphics↗

Stereoscopic depth cues can segment motion information.

Can the motion system selectively process elements at a particular depth? We attempted to answer this question using global coherence tasks in which signal and noise elements could be given different disparities. In experiment 1 we found that, if all the signal elements had a disparity different from that of the noise elements, performance was far better than when they had the same disparity (at least for stereo-normal observers). In a second experiment we found that adding additional noise elements to the motion task had no effect if they had a different disparity (however, they had a marked effect for stereo-blind observers). We conclude that stereo disparity can be used as a segmentation cue by the motion system.

Color Perception↗

Can one pay attention to a particular color?

In an array of elements whose colors vary can we selectively choose to process all the items of a particular color preferentially in relation to those of another color? We addressed this question by presenting subjects with arrays containing many elements, and recording reaction times to a luminance change of one of the elements. Half the elements had one color and the other half another color--the spatial distribution being random. In two tasks--a simple detection of this change or a choice reaction time to the polarity of the change--we found that reaction times were independent of the number of items in the array. Cuing the subjects as to the color of the target item had no significant influence on the detection task, but subjects were faster if cued for the discrimination task. A further experiment replicated these findings and examined possible costs and benefits. Our final experiment separated the roles of attentional guidance and postattentional processes by having subjects judge the orientation of the target element and varying the magnitude of the target flash that defined which element was the target. We found that this judgment was also affected by color cuing, and that the size of the effect interacted with the flash strength, suggesting that color cuing has its influence at the stage of attentional guidance. We conclude that subjects can selectively attend to items on the basis of color given the appropriate task and stimulus dynamics.

Attention↗

Shifts in perceived position following adaptation to visual motion.

Where do we perceive an object to be when it is moving? Nijhawan [1] has reported that if a stationary test pattern is briefly flashed in spatial alignment with a moving one, the moving element actually appears displaced in the direction in which it is moving. Nijhawan postulates that this may be the result of a mechanism that predicts the future position of the moving element so as to compensate for the fact that the element will have moved position from the time at which the light left it to the time at which the observer becomes aware of it (as a result of the finite time taken for neural transmission). There is an alternative explanation of this effect, however. Changes in the stimulus presentation could affect perceptual latency [2], and therefore the perceived position if in motion (as suggested for the Pulfrich pendulum effect [3] [4]). In other words, if the flashed probe of the Nijhawan demonstration takes longer to reach perceptual awareness than the moving stimulus, the latter will appear to be ahead of the probe. Here, I demonstrate an alternative way of testing this hypothesis. When an illusory movement is induced (via the motion aftereffect) within a stationary pattern, it can be shown that this also produces a change in its perceived spatial position. As the pattern is stationary, one cannot account for this result via the notion of perceptual lags.

Figural Aftereffect↗

The effects of surround contrast on contrast thresholds, perceived contrast and contrast discrimination.

Perceived contrast, contrast detection thresholds and contrast discrimination thresholds were measured in the presence and absence of surrounding patterns of a similar spatio-temporal makeup. In the foveal retina we found that the perceived contrast of the central pattern was reduced by the presence of the contrast surrounds with the effect being greatest at low test contrast. Detection thresholds were not affected and contrast discrimination thresholds were only affected over a small range of low test contrasts. However if the test pattern was made smaller, or if its central part was occluded detection thresholds were raised. In the peripheral retina detection thresholds were raised and discrimination thresholds were affected over most of the range of contrasts. We argue that the pattern of results resembles those produced in masking paradigms where the test and mask are coextensive if the spatial range of interactions is taken into account and hence the effects of the contrast surround may be merely a manifestation of normal masking processes.

Adult↗

Texture segregation and visual search: a comparison of the effects of random variations along irrelevant dimensions.

The effects of irrelevant variations in the color and depth of elements on participants' ability to detect and discriminate elements defined by a difference in orientation were compared. Consistent with previous research, it was found that there was no effect or small effects if the targets were single elements in visual search tasks and that there were large effects for targets defined by several elements defining an area in visual segmentation tasks. It is suggested that the reason for the discrepancy between the 2 paradigms lies in the need for grouping processes in segmentation experiments. This notion was examined in 3 additional experiments that manipulated grouping processes through task demands and stimulus design. The data provide tentative support for this notion.

Adult↗

Phantom motion after effects--evidence of detectors for the analysis of optic flow.

BACKGROUND: Electrophysiological recording from the extrastriate cortex of non-human primates has revealed neurons that have large receptive fields and are sensitive to various components of object or self movement, such as translations, rotations and expansion/contractions. If these mechanisms exist in human vision, they might be susceptible to adaptation that generates motion aftereffects (MAEs). Indeed, it might be possible to adapt the mechanism in one part of the visual field and reveal what we term a 'phantom MAE' in another part. RESULTS: The existence of phantom MAEs was probed by adapting to a pattern that contained motion in only two non-adjacent 'quarter' segments and then testing using patterns that had elements in only the other two segments. We also tested for the more conventional 'concrete' MAE by testing in the same two segments that had adapted. The strength of each MAE was quantified by measuring the percentage of dots that had to be moved in the opposite direction to the MAE in order to nullify it. Four experiments tested rotational motion, expansion/contraction motion, translational motion and a 'rotation' that consisted simply of the two segments that contained only translational motions of opposing direction. Compared to a baseline measurement where no adaptation took place, all subjects in all experiments exhibited both concrete and phantom MAEs, with the size of the latter approximately half that of the former. CONCLUSIONS: Adaptation to two segments that contained upward and downward motion induced the perception of leftward and rightward motion in another part of the visual field. This strongly suggests there are mechanisms in human vision that are sensitive to complex motions such as rotations.

Afterimage↗

Spatial frequency adaptation: threshold elevation and perceived contrast.

We have measured the spread of contrast adaptation across the dimension of spatial frequency. Threshold elevation was tightly tuned to the adapting spatial frequency but became much broader as test contrast was increased. This means that, for a given test frequency, there are some frequencies which do not raise threshold but do result in a loss of perceived contrast. The contrast dependence, retinal specificity and interocular transfer of adaptation effects elicited from same-and remote-frequency adaptation were compared. While we were able to show some distinct differences between threshold and suprathreshold tests, we were unable to demonstrate any reliable differences in the retinal specificity and interocular transfer between same- and remote-frequency adaptation.

Adaptation, Ocular↗

The processing of temporal modulation at different levels of retinal illuminance.

How does our temporal vision change as the mean illuminance reduces? We have examined the processing of near-threshold temporal information for a range of illuminance values (2850--0.15 phot td). At high illuminance, the modulation transfer function can be shown to be mediated via three underlying temporal filters that vary in sensitivity with spatial frequency. As the mean illuminance decreases these channels appear to change their sensitivity. Even at the lowest (scotopic) illuminance levels we were able to find evidence for at least two channels mediating detection threshold. There are also changes in the tuning properties of these channels such that the processing of high temporal frequencies is differentially compromised, resulting in a reduction in the flicker fusion limit of each channel, and a shift in the peak of the band-pass channel. The slope of the fall-off in sensitivity at high temporal frequencies is unaffected by test spatial frequency at each illuminance level, suggesting its limiting factor is one that is insensitive to spatial frequency. We propose that the changes in the tuning of the temporal filters occur because of an early (e.g. photoreceptor) change in the response dynamics, or by interactions between photoreceptors, rather than changes at or beyond the level of the channel response.

Adult↗

The effect of contrast adaptation on briefly presented stimuli.

Wilson and Humanski (1993) have recently reported evidence that adapting to low temporal frequency sinewave gratings yields little threshold elevation for briefly presented test stimuli. We postulated that brief stimuli may be detected by a transient channel which would be minimally affected by a low temporal frequency adapting pattern. We therefore measured the effect of adaptation on briefly presented test stimuli for a wider range of adapting temporal frequencies. The results indicate that adaptation may yield threshold elevation for briefly presented stimuli and that threshold elevation is greater for high than low temporal frequency adapting patterns. These results are consistent with the hypothesis that briefly presented stimuli are detected by a transient channel.

Adaptation, Ocular↗

Isolation and characteristics of a steady-state visually-evoked potential in humans related to the motion of a stimulus.

We have examined the visual potential evoked by two motion stimuli. In the first stimulus (termed coherent motion) a random-dot pattern oscillated between phases of coherent and incoherent ("snowstorm") motion, and in the second a random-dot pattern alternated in direction of motion (termed direction change). We found that the response to the coherent motion stimulus is low-pass with respect to speed, has low contrast sensitivity and increases steadily with the contrast of the stimuli. The direction change visually-evoked potential (VEP) is band-pass with respect to speed, has high contrast sensitivity but then saturates and even reduces as the stimulus contrast is raised above 0.1. The behaviour of the direction change VEP is similar in nature to results from psychophysical experiments of motion perception and to the known properties of directionally selective cells of the cortex. On the other hand the behaviour of the coherent motion VEP suggests this may not be mediated by a mechanism specific to motion.

Contrast Sensitivity↗

Perceived contrast as a function of adaptation duration.

We measured how the perceived contrast of a sinusoidal grating fades as a function of time. Measurements were made for a range of temporal and spatial frequencies and eccentricities. Patterns of high temporal and low spatial frequency exhibited a greater and more rapid loss of apparent contrast (fade) than those of medium frequencies. The rate and amount of fading for a subgroup of moderate frequencies increased when presented peripherally rather than foveally. Further measurements revealed that gratings of disparate spatial frequencies, but with the same threshold sensitivity, exhibit very different fading characteristics but equal threshold elevation. We conclude that the differential loss of apparent contrast is not an artefact of differing proximities to threshold, nor can it be accounted for by differences in the adaptability of underlying spatio-temporal mechanisms at threshold. The differences in fading may thus reflect either a difference in the adaptability of underlying channels above threshold or a differential contribution of such channels to perceived contrast.

Adaptation, Ocular↗

Is global motion really based on spatial integration of local motion signals?

Previous studies have shown that a random-dot kinematogram (RDK) comprising dots, each of which takes a random walk in direction or speed over time, can appear to flow in a single direction. This has been interpreted as evidence for the existence of a co-operative network linking neurons sensitive to different directions/speeds and different spatial locations. We have investigated the possibility that global motion perception in such patterns might simply reflect motion energy detection at a coarse spatial scale (such that many dots fall in the receptive field of one energy detector) without the need to encode local dot motions on a fine spatial scale and then integrate their motions over space. We created random-walk RDKs and then spatially high-pass filtered them to remove low spatial frequencies. Perception of global motion was unimpaired for both direction and speed random walks, showing that the phenomenon is not reliant on low spatial frequencies and must, therefore, involve integration of local motion signals across space, as originally postulated.

Discrimination, Psychological↗