The Motion Analogue of the Café Wall Illusion

Perception ◽  
1997 ◽  
Vol 26 (5) ◽  
pp. 569-584 ◽  
Author(s):  
Tatsuto Takeuchi

Detecting visual motion is computationally equivalent to detecting spatiotemporally oriented contours. The question addressed in this study is whether the illusory oriented contour in the space–space domain induces corresponding illusory motion perception. Two experiments were conducted. In experiment 1, the Café Wall pattern, which elicits a strong illusion of orientation (Café Wall illusion), was found to induce an illusion of motion when this pattern was converted to the space – time domain. The strength of the motion illusion depends on the mortar luminance and width, as for the Café Wall illusion. In experiment 2, the adaptation to this illusion of motion was found to induce a motion aftereffect in a static test, which indicates that a first-order-motion system contributes to the induction of the motion illusion. In fact, the motion-energy model was able to predict the strength of this motion aftereffect.

2002 ◽  
Vol 13 (1) ◽  
pp. 75-84 ◽  
Author(s):  
Yuji Kobayashi ◽  
Aihide Yoshino ◽  
Tsuneyuki Ogasawara ◽  
Soichiro Nomura

2013 ◽  
Vol 26 (4) ◽  
pp. 317-332 ◽  
Author(s):  
Yasuhiro Takeshima ◽  
Jiro Gyoba

Several studies have examined the effects of auditory stimuli on visual perception. In studies of cross-modal correspondences, auditory pitch has been shown to modulate visual motion perception. In particular, low-reliability visual motion stimuli tend to be affected by metaphorically or physically congruent or incongruent sounds. In the present study, we examined the modulatory effects of auditory pitch on visual perception of motion trajectory for visual inputs of varying reliability. Our results indicated that an auditory pitch implying the illusory motion toward the outside of the visual field-modulated perceived motion trajectory. In contrast, auditory pitch implying the illusory motion toward the central visual field did not affect the perception of motion trajectory. This asymmetrical effect of auditory stimuli occurred depending on the reliability of the visual input. Moreover, sounds that corresponded in terms of their pitch-elevation mapping altered the perception of the trajectory of visual motion when apparent motion could be perceived smoothly. Therefore, the present results demonstrate that auditory stimuli modulate visual motion perception especially when smooth motion is perceived in the peripheral visual field.


2019 ◽  
Author(s):  
Ahmad Yousef

This article is to provide evidence that deep breathing had great influence on the perception of stimuli that trigger illusory motion perception. We had used two different stimuli; the first one can be considered as bistable rivalrous stimulus because it can trigger illusory motion reversals during its motion. The second stimulus is stationary, namely rotating snakes illusion, it is also bistable rivalrous stimulus because it has two states, stationary versus illusory motion. We had noticed that deep inhalation slows down the speed of the first stimulus and eliminates the illusory motion perception of the second stimulus. This might be because the amount of the hobgoblin red blood cells, possibly including the rich oxygenated ones, might be forcibly reduced in the brain during the intended inhalation, in turn, different parts in the brain, including hMT+ region, might be partially deactivated, see reference 1 and 2. Significant reduction against stimulus’ contrast is known to slow down the perceived speed, it also diminishes the activities of the retinal peripheries and their corresponding neurological connections that collectively build up the peripheral brain; we therefore suspect the peripheral hMT+ region to be inactivated by the deep inhalation. Strong exhalation, however, triggers illusory motion reversal for the first stimulus, and promotes illusory motion perception for the second stimulus; behavior that can be explained by the increased amount of the hobgoblin red blood cells that may activate different necessary regions in the peripheral brain. Astonishingly, we found that deep inhalation and exhalation sufficiently can control the aforementioned bistable visual perception.


Perception ◽  
10.1068/p5037 ◽  
2003 ◽  
Vol 32 (4) ◽  
pp. 475-484 ◽  
Author(s):  
Michiteru Kitazaki ◽  
Takao Sato

Attentional effects on self-motion perception (vection) were examined by using a large display in which vertical stripes containing upward or downward moving dots were interleaved to balance the total motion energy for the two directions. The dots moving in the same direction had the same colour, and subjects were asked to attend to one of the two colours. Vection was perceived in the direction opposite to that of non-attended motion. This indicates that non-attended visual motion dominates vection. The attentional effect was then compared with effects of relative depth. Clear attentional effects were again found when there was no relative depth between dots moving in opposite directions, but the effect of depth was much stronger for stimuli with a relative depth. Vection was mainly determined by motion in the far depth plane, although some attentional effects were evident even in this case. These results indicate that attentional modulation for vection exists, but that it is overridden when there is a relative depth between the two motion components.


Perception ◽  
1994 ◽  
Vol 23 (10) ◽  
pp. 1257-1264 ◽  
Author(s):  
Michael T Swanston

Evidence concerning the origin of the motion aftereffect (MAE) is assessed in terms of a model of levels of representation in visual motion perception proposed by Wade and Swanston. Very few experiments have been designed so as to permit unambiguous conclusions to be drawn. The requirements for such experiments are identified. Whereas retinocentric motion could in principle give rise to the MAE, data are not available which would enable a conclusion to be drawn. There is good evidence for a patterncentric origin, indicating that the MAE is primarily the result of adaptation in the systems responsible for detecting relative visual motion. There is evidence for a further contribution from the process that compensates retinocentric motion for eye movements, in the form of nonveridical information for eye movements. There may also be an effect at the level at which perceived distance and self-movement information are combined with egocentric motion to give a geocentric representation which provides the basis for reports of phenomenal experience. It is concluded that the MAE can be caused by changes in activity at more than one level of representation, and cannot be ascribed to a single underlying process.


2003 ◽  
Vol 14 (4) ◽  
pp. 357-361 ◽  
Author(s):  
Jean Vroomen ◽  
Beatrice de Gelder

In this study, we show that the contingent auditory motion aftereffect is strongly influenced by visual motion information. During an induction phase, participants listened to rightward-moving sounds with falling pitch alternated with leftward-moving sounds with rising pitch (or vice versa). Auditory aftereffects (i.e., a shift in the psychometric function for unimodal auditory motion perception) were bigger when a visual stimulus moved in the same direction as the sound than when no visual stimulus was presented. When the visual stimulus moved in the opposite direction, aftereffects were reversed and thus became contingent upon visual motion. When visual motion was combined with a stationary sound, no aftereffect was observed. These findings indicate that there are strong perceptual links between the visual and auditory motion-processing systems.


1967 ◽  
Vol 24 (3_suppl) ◽  
pp. 1263-1270 ◽  
Author(s):  
Thomas R. Scott ◽  
Robert A. Bragg ◽  
Augustus E. Jordan

Eysenck's claim that sodium amytal shortens and dexedrine lengthens the duration of spiral aftereffect was not borne out in any of four experiments designed to demonstrate it, including a replication of his study. A further replication, different only in the stimulus used, yielded no effect of amytal or dexedrine. Actual measurement of aftereffect rate immediately following the eliciting stimulus and after selected delays showed an exponential decay function for aftereffect rate but did not demonstrate any effect of the two drugs. This repeated failure to demonstrate a change in aftereffect as a result of the administration of drugs known to affect neuron firing thresholds has implications for the understanding of neurophysiology of visual motion perception. It was proposed that motion aftereffect is based on a comparison of the states of two neural systems both of which are equally affected by the drugs.


2020 ◽  
Vol 14 ◽  
Author(s):  
Junxiang Luo ◽  
Zheyuan Chen ◽  
Yiliang Lu ◽  
Lothar Spillmann ◽  
Ian Max Andolina ◽  
...  

In a pattern of horizontal lines containing ± 45° zigzagging phase-shifted strips, vivid illusory motion is perceived when the pattern is translated up or down at a moderate speed. Two forms of illusory motion are seen: [i] a motion “racing” along the diagonal interface between the strips and [ii] lateral (sideways) motion of the strip sections. We found the relative salience of these two illusory motions to be strongly influenced by the vertical spacing and length of the line gratings, and the period length of the zigzag strips. Both illusory motions are abolished when the abutting strips are interleaved, separated by a gap or when a real line is superimposed at the interface. Illusory motion is also severely weakened when equiluminant colored grating lines are used. Illusory motion perception is fully restored at < 20% luminance contrast. Using adaptation, we find that line-ends alone are insufficient for illusory motion perception, and that both physical carrier motion and line orientation are required. We finally test a classical spatiotemporal energy model of V1 cells that exhibit direction tuning changes that are consistent with the direction of illusory motion. Taking this data together, we constructed a new visual illusion and surmise its origin to interactions of spatial and temporal energy of the lines and line-ends preferentially driving the magnocellular pathway.


1999 ◽  
Vol 81 (1) ◽  
pp. 388-393 ◽  
Author(s):  
Jody C. Culham ◽  
Sean P. Dukelow ◽  
Tutis Vilis ◽  
Frank A. Hassard ◽  
Joseph S. Gati ◽  
...  

Culham, Jody C., Sean P. Dukelow, Tutis Vilis, Frank A. Hassard, Joseph S. Gati, Ravi S. Menon, and Melvyn A. Goodale. Recovery of fMRI activation in motion area MT following storage of the motion aftereffect. J. Neurophysiol. 81: 388–393, 1999. We used functional magnetic resonance imaging (fMRI) during storage of the motion aftereffect (MAE) to examine the relationship between motion perception and neural activity in the human cortical motion complex MT+ (including area MT and adjacent motion-selective cortex). MT+ responds not only to physical motion but also to illusory motion, as in the MAE when subjects who have adapted to continuous motion report that a subsequent stationary test stimulus appears to move in the opposite direction. In the phenomenon of storage, the total decay time of the MAE is extended by inserting a dark period between adaptation and test phases. That is, when the static test pattern is presented after a storage period equal in duration to the normal MAE, the illusory motion reappears for almost as long as the original effect despite the delay. We examined fMRI activation in MT+ during and after storage. Seven subjects viewed continuous motion, followed either by an undelayed stationary test (immediate MAE) or by a completely dark storage interval preceding the test (stored MAE). Like the perceptual effect, activity in MT+ dropped during the storage interval then rebounded to reach a level much higher than after the same delay without storage. Although MT+ activity was slightly enhanced during the storage period following adaptation to continuous motion (compared with a control sequence in which the adaptation grating oscillated and no MAE was perceived), this enhancement was much less than that observed during the perceptual phenomenon. These results indicate that following adaptation, activity in MT+ is pronounced only with the presentation of an appropriate visual stimulus, during which the MAE is perceived.


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