Similarity between Petter's effect and visual phantoms

Here we draw attention to similarity between Petter's effect and the visual phantom illusion. Phantoms are visible when the spatial frequency of the inducing grating is low or the occluder is thin, whereas phantoms are invisible when the spatial frequency of the inducing grating is high or the occluder is thick. Moreover, phantoms are perceived in front of the occluder when they are visible, whereas the occluder is seen in front of the inducing gratings when phantoms are invisible. These characteristics correspond to Petter's effect, in which the thicker region tends to be perceived in front of the thinner region when two regions of the same lightness and of different sizes overlap, since 'thick' corresponds to low spatial frequency of the inducing grating or a thick occluder while 'thin' corresponds to high spatial frequency of the inducing grating or a thin occluder.     

Perception of visual speed while moving

During self-motion, the world normally appears stationary. In part, this may be due to reductions in visual motion signals during self-motion. In 8 experiments, the authors used magnitude estimation to characterize changes in visual speed perception as a result of biomechanical self-motion alone (treadmill walking), physical translation alone (passive transport), and both biomechanical self-motion and physical translation together (walking). Their results show that each factor alone produces subtractive reductions in visual speed but that subtraction is greatest with both factors together, approximating the sum of the 2 separately. The similarity of results for biomechanical and passive self-motion support H. B. Barlow's (1990) inhibition theory of sensory correlation as a mechanism for implementing H. Wallach's (1987) compensation for self-motion.     

Perceptual continuation and depth in visual phantoms can be explained by perceptual transparency

We try to explain perceptual continuation and depth in the visual-phantom illusion in terms of perceptual transparency. Perceptual continuation of inducing gratings across the occluder in stationary phantoms could be explained with unique transparency, a notion proposed by Anderson (1997 Perception 26 419-453). This view is consistent with a number of previous reports including that of McCourt (1994 Vision Research 34 1609-1617) who criticized the stationary phantom illusion from the viewpoint of his counterphase lightness induction or grating induction, which might involve invalid transparency. Here we confirm that the photopic phantom illusion (Kitaoka et al, 1999 Perception 28 825-834) really gives in-phase lightness induction and involves bistable transparency. It is thus suggested that perceptual continuation and depth in the visual-phantom illusion depend on perceptual transparency.     

Visual behavior and perception of trajectories of moving objects with visual occlusion

Experienced athletes in sports with moving objects have shown greater skill when using visual information to anticipate the direction of a moving object than nonexperienced athletes of those sports. Studies have shown that expert athletes are more effective than novices in occlusion situations in the first stages of the sports sequence. In this study, 12 athletes with different competitive experience in sports with moving objects viewed a sequence of tennis ball launches with and without visual occlusion, launched by a ball-shooting machine toward different areas with respect to the participant's position. The relation among visual behavior, occlusion time, and the precision of the task is reviewed. The spot where the balls bounced was analysed by a digital camera and visual behavior by an Eye Tracking System. Analysis showed that the nonexperienced athletes made significantly more errors and were more variable in visual occlusion conditions. Participants had a stable visual search strategy.     

Components of reflexive visual orienting to moving objects

Posner and Cohen (1984) and Maylor (1985) initially observed that a luminance change produces both facilitatory and inhibitory effects on subsequent detection. While Posner and Cohen claimed that the facilitatory effect was mapped in retinotopic coordinates, they showed that inhibition of return (IOR) was mapped in “environmental coordinates.” Tipper and colleagues (Tipper, Driver, & Weaver, 1991; Tipper et al., 1997; Tipper, Weaver, Jerreat, & Burak, 1994) and Abrams and Dobkin (1994b) have recently reported that IOR can be object based, but contradictory results have also been reported (Muller & von Mühlenen, 1996). Here we report six experiments showing that an uninformative peripheral cue can generate either facilitatory or inhibitory object-based effects that can tag moving objects and that can persist for several hundred milliseconds. Although the boundary conditions determining which effect will be manifest remain to be defined, the present results suggest that facilitation and inhibition are generated independently, rather than being components of the same biphasic process.     

Dynamic visual capture: apparent auditory motion induced by a moving visual target

Apparent motion of a sound source can be induced by a moving visual target. The direction of the perceived motion of the sound source is the same as that of the visual target, but the subjective velocity of the sound source is 25-50% of that of the visual target measured under the same conditions. Eye tracking of the light target tends to enhance the apparent motion of the sound, but is not a prerequisite for its occurrence. The findings are discussed in connection with the 'visual capture' or 'ventriloquism' effect.     

Attention level oscillations during visual perception of moving stimuli

Optokinetic nystagmus (OKN) pursuit phase velocity oscillations were studied in seven undergraduates during repeated 4 min presentation of optokinetic stimuli. The following variable parameters of the stimuli motion were used with each subject: horizontal direction, angular velocity (AV), and frequency-to-velocity ratio. AV of the OKN pursuit phases was found to decrease markedly within the first 30 sec of stimuli presentation with its successive increase and variously marked oscillations. Gradual decrease of the AV of OKN pursuit phases was observed at the end of the whole examination as compared to its beginning already within 4 min presentation of the moving stimuli. The results are discussed from the point of view of the arousal, and the activation components of visual attention.     

Infant responses of ocular fixation to moving visual stimuli

Infants of 1, 2, and 3 months of age were presented with two checkerboard patterns, one stationary and the other moving in a horizontal oscillatory motion at one of eight rates. An observer who could see only the infant's head and eyes recorded, for each 30-sec trial, (a) the position of first fixation, (b) position of fixation at the end of each 5-sec interval, and (c) a final forced-choice judgment of the position of the moving stimulus. Results showed reliable differences in ocular behavior as a function of rate of stimulus motion for all three groups of infants.     

Components of reflexive visual orienting to moving objects.

Posner and Cohen (1984) and Maylor (1985) initially observed that a luminance change produces both facilitatory and inhibitory effects on subsequent detection. While Posner and Cohen claimed that the facilitatory effect was mapped in retinotopic coordinates, they showed that inhibition of return (IOR) was mapped in "environmental coordinates." Tipper and colleagues (Tipper, Driver, & Weaver, 1991; Tipper et al., 1997; Tipper, Weaver, Jerreat, & Burak, 1994) and Abrams and Dobkin (1994b) have recently reported that IOR can be object based, but contradictory results have also been reported (Müller & von Mühlenen, 1996). Here we report six experiments showing that an uninformative peripheral cue can generate either facilitatory or inhibitory object-based effects that can tag moving objects and that can persist for several hundred milliseconds. Although the boundary conditions determining which effect will be manifest remain to be defined, the present results suggest that facilitation and inhibition are generated independently, rather than being components of the same biphasic process.     

Aging and visual marking: selective deficits for moving stimuli

The selective processing of new visual information can be facilitated by the top-down inhibition of old stimuli already in the visual field, a capacity-limited process termed visual marking (D. G. Watson & G. W. Humphreys, 1997). Three experiments assessed the effects of aging on visual marking using stationary (Experiment 1) and moving (Experiments 2 and 3) items. For young participants, visual marking was observed in all experiments. For older participants, visual marking was observed only with stationary items. The results are not consistent with any simple account of general age-related decrements and provide further support for the deployment of different methods of visual marking depending on the properties of the old items and the current task demands.     

Amodal completion and visual holes (static and moving)

Occlusion is a frequent occurrence in a cluttered world of opaque objects. Often information about the shape of partly occluded objects can be gathered from the visible portion of the object and in particular its contours. Here we address the case where a region of a surface is visible exclusively through an aperture (visual hole). We make several observations about the grouping of surface regions visible through holes, and the appearance of moving objects and holes. These observations support the view that holes are shape properties of the object-with-hole.     

Relative locations among moving spots and visual vector analysis.

How the direction of apparent movement changed with the relative locations among spots was quantitatively measured by the method proposed by Hochberg and Fallon. From the vector-extraction model (proposed by Johansson) expanded as, "The vector to be subtracted depends on the relative location." and the directions of apparent movement, the vector to be subtracted was calculated at each relative location. Consequently data showed (i) the region in which the directions of spots in motion are affected by the frame is finite, and (ii) the degree of the influence is not iniform in the region but is rapidly reduced as spots go away from the frame.     

A comparison of auditory and visual apparent motion presented individually and with crossmodal moving distractors

Unimodal auditory and visual apparent motion (AM) and bimodal audiovisual AM were investigated to determine the effects of crossmodal integration on motion perception and direction-of-motion discrimination in each modality. To determine the optimal stimulus onset asynchrony (SOA) ranges for motion perception and direction discrimination, we initially measured unimodal visual and auditory AMs using one of four durations (50, 100, 200, or 400 ms) and ten SOAs (40-450 ms). In the bimodal conditions, auditory and visual AM were measured in the presence of temporally synchronous, spatially displaced distractors that were either congruent (moving in the same direction) or conflicting (moving in the opposite direction) with respect to target motion. Participants reported whether continuous motion was perceived and its direction. With unimodal auditory and visual AM, motion perception was affected differently by stimulus duration and SOA in the two modalities, while the opposite was observed for direction of motion. In the bimodal audiovisual AM condition, discriminating the direction of motion was affected only in the case of an auditory target. The perceived direction of auditory but not visual AM was reduced to chance levels when the crossmodal distractor direction was conflicting. Conversely, motion perception was unaffected by the distractor direction and, in some cases, the mere presence of a distractor facilitated movement perception.     

The effect of moving and static trans-scleral illumination of visual afterimages

The inside of the eye was illuminated by shining a small light through the upper eyelid and the sclera. After viewing a bright light flash, Ss closed their eyes and reported the duration of the afterimage under the following conditions: the light on and moving across the S’s eyelid (moving trans-scleral illumination), the light on but stationary (static trans-scleral illumination), and two corresponding control conditions in which the light was turned off (darkness). Results indicate that when the trans-scleral light is moving, afterimages are seen clearly for periods of approximately the same duration as those seen in complete darkness. However, when the trans-scleral illumination is stationary, the duration of the afterimages is significantly reduced. These results are compatible with other afterimage data that suggest that changes within the field after initial stimulation are needed to prolong afterimages.     

Judgments of synchrony between auditory and moving or still visual stimuli.

The flash-lag effect is a visual illusion wherein intermittently flashed, stationary stimuli seem to trail after a moving visual stimulus despite being flashed synchronously. We tested hypotheses that the flash-lag effect is due to spatial extrapolation, shortened perceptual lags, or accelerated acquisition of moving stimuli, all of which call for an earlier awareness of moving visual stimuli over stationary ones. Participants judged synchrony of a click either to a stationary flash of light or to a series of adjacent flashes that seemingly bounced off or bumped into the edge of the visual display. To be judged synchronous with a stationary flash, audio clicks had to be presented earlier--not later--than clicks that went with events, like a simulated bounce (Experiment 1) or crash (Experiments 2-4), of a moving visual target. Click synchrony to the initial appearance of a moving stimulus was no different than to a flash, but clicks had to be delayed by 30-40 ms to seem synchronous with the final (crash) positions (Experiment 2). The temporal difference was constant over a wide range of motion velocity (Experiment 3). Interrupting the apparent motion by omitting two illumination positions before the last one did not alter subjective synchrony, nor did their occlusion, so the shift in subjective synchrony seems not to be due to brightness contrast (Experiment 4). Click synchrony to the offset of a long duration stationary illumination was also delayed relative to its onset (Experiment 5). Visual stimuli in motion enter awareness no sooner than do stationary flashes, so motion extrapolation, latency difference, and motion acceleration cannot explain the flash-lag effect.     

Parallel ocular and manual tracking responses to a continuously moving visual target

Continuous ocular and manual tracking of the same visual target moving horizontally in sinusoids at 0.75 Hz was measured by lag, RMS Error, and Gain. The best measures of accuracy of tracking, error and lag, were remarkably similar in the two systems and were affected similarly by presence of a background and changes in predictability of target movement. Details of within-system performance varied despite the over-all parallels. Gain was different in adjustment of proportion of saccadic to pursuit movement was affected by the presence of the hand, even though this did not affect tracking accuracy. The over-all parallel of response adjustment suggests that a suprasystem decision-maker sets general response goals and each motor system adjusts output details to match these goals.