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The Ouchi illusion: an anomaly in the perception of rigid motion for limited spatial frequencies and angles.

The spatial parameters underlying a novel illusion of relative motion are characterized. A simple stimulus composed of two sine-wave gratings was sufficient to generate the illusion. We measured the response of subjects to rapid, small-amplitude oscillations of this stimulus behind a fixation point. The effect was clearly strongest for acute angles between the gratings, but only when spatial frequency was between 6 and 11 cpd. We surmise that activity in the grating cells of the primate visual cortex (von der Heydt, Peterhans, & Dursteler, 1992) might be the cause of the illusion. The illusion is potentially an important tool in understanding how higher cortical areas combine disparate motion signals.

Humans↗

Pharmacological properties of motion vision in goldfish measured with the optomotor response.

In goldfish, the retinal pathways involved in motion coding have been demonstrated to have an L-cone dominated action spectrum (S. Schaerer, C. Neumeyer, Motion detection in goldfish investigated with the optomotor response is "color blind", Vision Res. 36 (1996) 4025-4034). The neurotransmitters involved in retinal motion coding mechanisms, and the relevance of these retinal motion coding mechanisms for motion perception, are little investigated in fish. In this study, the optomotor response was used to investigate the effect of antagonists on different receptor types for acetylcholine (ACh), GABA, for the dopamine D2-receptor (D2-R) - which is known to modulate the action spectrum in motion coding (C. Mora-Ferrer, K. Behrend, Dopaminergic modulation of photopic temporal transfer properties in goldfish retina investigated with the ERG, Vision Res. 44 (2004) 2067-2081) - and of an agonist for against the mGluR6-receptor (mGluR6) on goldfish motion vision in the photopic range. Blockade of nicotinic ACh-R, GABAa-R and both GABAa- and GABAc-R eliminated the optomotor response completely. Neither a muscarinic ACH-R antagonist, a D2-R antagonist or a mGluR6-agonist affected goldfish motion vision. The pharmacological profile of the goldfish optomotor response resembles the pharmacological profile of direction-selective ganglion cells (DS-GC) described for vertebrate retinas in electrophysiological experiments, e.g. (S. Weng, W. Sun, S. He, Identification of ON-OFF direction-selective ganglion cells in the mouse retina, J. Physiol. 562 (2005) 915-923). This indicates that cells with direction-selective receptive field properties exist in the goldfish retina. It is proposed that these cells provide the input for the full field motion perception in goldfish.

Acetylcholine↗

Smooth anticipatory eye movements alter the memorized position of flashed targets.

Briefly flashed visual stimuli presented during smooth object- or self-motion are systematically mislocalized. This phenomenon is called the "flash-lag effect" (Nijhawan, 1994). All previous studies had one common characteristic, the subject's sense of motion. Here we asked whether motion perception is a necessary condition for the flash-lag effect to occur. In our first experiment, we briefly flashed a target during smooth anticipatory eye movements in darkness and subjects had to orient their gaze toward the perceived flash position. Subjects reported to have no sense of eye motion during anticipatory movements. In our second experiment, subjects had to adjust a cursor on the perceived position of the flash. As a result, we show that gaze orientation reflects the actual perceived flash position. Furthermore, a flash-lag effect is present despite the absence of motion perception. Moreover, the time course of gaze orientation shows that the flash-lag effect appeared immediately after the egocentric to allocentric reference frame transformation.

Adult↗

Human colour discrimination based on a non-parvocellular pathway.

BACKGROUND: Traditionally, colour information is assumed to be carried by neural channels in the parvocellular pathway and to be encoded in an opponent manner, while other, non-parvocellular, spectrally non-opponent channels are thought to play no part in colour vision. But is the parvocellular pathway the only way that colours can be discriminated in human vision? We studied two patients with cerebral achromatopsia, who lack conscious colour perception but are nevertheless able to make use of colour information. In particular, we investigated whether, in these patients, colour discrimination is mediated by the parvocellular pathway. RESULTS: The achromatopsic patients carried out a forced-choice colour- and luminance-discrimination task, and showed clear evidence of unconscious colour processing, consistent with previous studies. We added different types of luminance noise to see when this unconscious colour information could be masked. The results of the colour-discrimination-with-noise and the brightness-non-additivity experiments showed a double-dissociation between patients. This indicates that, in one patient, unconscious colour discrimination may be subserved by a spectrally non-opponent mechanism, which does not have the characteristics of the parvocellular pathway and which is responsive to fast flicker. Spectral sensitivity, contrast sensitivity and motion perception experiments confirmed that this patient lacks a working opponent parvocellular system. The second achromatopsic patient showed evidence of a residual parvocellular system. CONCLUSIONS: Our results show that chromatic discrimination need not be mediated by neural mechanisms, the parvocellular system in particular, normally assumed to subserve conscious colour perception. Such discrimination may be mediated by a neural subsystem which responds to fast flicker, is spectrally non-opponent, and supports normal motion perception.

Aged↗

Perceived motion direction during smooth pursuit eye movements.

Although many studies have been devoted to motion perception during smooth pursuit eye movements, relatively little attention has been paid to the question of whether the compensation for the effects of these eye movements is the same across different stimulus directions. The few studies that have addressed this issue provide conflicting conclusions. We measured the perceived motion direction of a stimulus dot during horizontal ocular pursuit for stimulus directions spanning the entire range of 360 degrees. The stimulus moved at either 3 or 8 degrees/s. Constancy of the degree of compensation was assessed by fitting the classical linear model of motion perception during pursuit. According to this model, the perceived velocity is the result of adding an eye movement signal that estimates the eye velocity to the retinal signal that estimates the retinal image velocity for a given stimulus object. The perceived direction depends on the gain ratio of the two signals, which is assumed to be constant across stimulus directions. The model provided a good fit to the data, suggesting that compensation is indeed constant across stimulus direction. Moreover, the gain ratio was lower for the higher stimulus speed, explaining differences in results in the literature.

Adolescent↗

The effect of spatial parameters on oscillatory movement displacement thresholds.

Earlier work has established that oscillatory movement displacement thresholds (OMDT) are a form of hyperacuity. There is speculation that the mechanism determining OMDT, like motion perception in general, involves direct motion sensing at high temporal frequencies of oscillation and spatial localization processes (from which motion is inferred) at low temporal frequencies, which are both hyperacuities in their own right. OMDT were determined, for three experienced observers, over the temporal frequency range 1-15 Hz, for three stimulus lengths and three stimulus widths. Both decreasing stimulus length and decreasing stimulus width increased OMDT at all temporal frequencies. Furthermore, the resulting functions consistently exhibit a "kink" in the temporal frequency midrange. The results are interpreted as evidence that there are two subsystems involved in the analysis of visual motion with the kink indicating the transition where one system begins to predominate over the other.

Humans↗

Radial motion looks faster.

Current models of motion perception depend on unidirectional motion-sensitive mechanisms that provide local inputs for complex pattern motion, such as optic flow. To test the generality of such models, we asked observers to compare the speed of radial gratings with the translational speed of vertical gratings. The speed of the radial gratings was consistently overestimated by 20-60% relative to that of translating gratings that were identical in all other respects. The speed bias was not associated with a general spatial or temporal processing bias, nor with the high relative speed of points about the center of expansion/contraction. The bias increased non-linearly with the size of sectors of the radiating pattern exposed. As the motion of the two patterns was locally identical but judged differently, the apparent speed of both kinds of motion cannot be served by any mechanism, nor described by any model, that is based entirely on local motion signals. We speculate that the greater apparent speed of the radial motion has to do with apparent motion in depth.

Humans↗

Visual stabilization of posture. Physiological stimulus characteristics and clinical aspects.

Visual stabilization of posture is critically dependent on stimulus characteristics as well as on the performance of the visual system. The purpose of the present investigation was to obtain quantitative data in man by means of posturography of fore-aft and lateral body sway in relation to different visual stimulus characteristics. Visual acuity, when decreased logarithmically, causes a linearly increasing postural instability, twice as prominent for fore-aft than for lateral sway. Any measurable visual contribution for fore-aft sway ceases with an acuity lower than 0.03 and for lateral sway with an acuity lower than 0.01. The central area of the visual field as compared with the peripheral retina dominates postural control. The foveal region exhibits a powerful contribution, in particular for lateral sway. A partial but significant visual stabilization is preserved with a visual input rate between 1 to 4 Hz flicker frequency. As soon as continuous motion perception becomes involved with frequencies higher than 4 Hz, visual stabilization gradually improves with a saturation at frequencies higher than 16 Hz. Lateral body sway activity and eye-object distance are linearly related: body sway decreases with increasing distance corresponding to the linear decrease of net retinal displacement with increasing eye-object distance. Aspects of 'afferent' and 'efferent' visual motion perception, which involve fore-aft and lateral body sway differently, are evaluated. The clinical relevance is demonstrated in patients with oculomotor disturbances. The results are discussed with respect to the variety of related clinical disorders, which involve reduction in visual acuity, field defects, accommodation disturbances and ocular oscillations.

Accommodation, Ocular↗

Viewing-distance invariance of movement detection.

Since visual movement information is often presented in electronic displays or films it is amazing that there is a paucity of research on the influence of viewing distance on motion detection in cinematograms. We report a relatively high degree of detection constancy with changing viewing distance for coherent motion in random-pixel cinematograms. A constant performance irrespective of viewing-distance is called 'distance-invariance' and for motion detection it proves to hold reasonably well for a relatively wide range of viewing distances both for foveal and eccentric vision. The limits of this viewing-distance invariance are explored as a function of screen velocity. Detection performance is quantified by a threshold signal-to-noise-ratio (SNR-) value, S, which is determined as a function of velocity for a range of viewing distances from 53 to 13,476 mm for foveal vision and from 60 to 1925 mm at 24 degrees eccentricity on the nasal horizontal meridian of the right eye's retina. The data can be explained, at least qualitatively, by a model in which a spatial-resolution stack has a stack of velocity-tuned motion detectors at every resolution layer. Such a 'stack-of-stacks' model is in line with proposals for contrast-detection stack-models, but it suggests that the usual hypothesis that motion perception is based on the activity of two separate systems, the short-range and the long-range system, might be superfluous. This two-systems distinction was largely based on the different performance found for moving random dot patterns and moving form-defined stimuli. A moving random pixel array viewed at very close range (e.g. 6 cm) presents the subject with relatively large almost square 'blobs', which are less dissimilar from the phi-stimuli used in classic motion perception studies than random dot stimuli at the usual medium to large viewing distances. It leads to maximum displacement threshold (Dm-) values that are not untypical of the 'long-range' system, but by gradually increasing the viewing-distance and thus decreasing the pixel-size a continuous change is found from typical long-range to typical short-range values of Dm. The two-systems distinction for motion detection appears to refer to the stimulus rather than to the visual system: The motion-detection system might be forced into a local or a global 'mode of operation' by the choice of stimulus.

Female↗

Clinical significance of perceptible fetal motion.

The monitoring of fetal activity during the last trimester of pregnancy has been proposed to be useful in assessing fetal welfare. The maternal perception of fetal activity was tested among 82 patients using real-time ultrasonography. All perceived fetal movements were visualized on the scanner and involved motion of the lower limbs. Conversely, 82% of all visualized motions of fetal limbs were perceived by the patients. All combined motions of fetal trunk with limbs were preceived by the patients and described as strong movements, whereas clusters of isolated, weak motions of the fetal limbs were less accurately perceived (56% accuracy). The number of fetal movements perceived during the 15-minute test period was significantly (p < 0.001) greater in pregnancies with ruptured amniotic membranes (9.2 +/- 1.8) than in those with intact membranes (4.2 +/- 0.6). A favorable neonatal outcome was more common (p < 0.01) when recent visualized strong fetal motion was present (44 of 45 cases) than when it was absent (five of 10 cases). These findings reveal that perceived fetal motion is: (1) reliable; (2) related to the strength of lower limb motion; (3) increased with ruptured amniotic membranes; and (4) reassuring if considered to be active.

Female↗

Expansion of visual space after saccadic eye movements.

Human subjects reported the perceived two-dimensional location of a visual target that was briefly presented after a saccade in the absence of visual references. Consistent with previous studies, immediately after horizontal saccades, there was a salient horizontal component in mislocalization in the direction opposite to the saccade. However, the horizontal component in mislocalization was not constant and was larger for targets presented further into the visual field contraversive to the saccade. For the same horizontal saccades, the vertical component in mislocalization was also obvious, and it was larger for targets located further away from the saccade trajectory. The saccadic effects resulted in an overall pattern of mislocalization that could be best described as a two-dimensional expansion of visual space. The point of expansive origin was not associated with the saccade goal, but was shifted from the saccade goal in the direction of the saccade. These results suggest that spatial information processing at the time of saccades reflects topographic interactions between neural activations from saccade execution and the visual target. The configuration of mislocalized positions of single point stimuli along a line was not comparable to the pattern of non-veridical motion perception described by Park, Lee & Lee (2001), indicating that spatial mislocalization and non-veridical motion perception after saccades are independent phenomena.

Adult↗

Reduced duration of a visual motion aftereffect in congenital nystagmus.

Congenital nystagmus (CN) is a primarily horizontal, involuntary, conjugate eye movement which can be observed soon after birth or during the first half-year of life. Individuals with CN rarely complain of oscillopsia. Using a motion aftereffect (MAE), we investigated if individuals with CN have abnormalities in motion perception and if any such abnormality could be due to nystagmus or to compensatory mechanisms to avoid oscillopsia. In task A, patients (n=10) and control subjects (n=10) indicated the direction, duration and relative velocity of MAEs. The subjects binocularly viewed a high contrast, grey scale grating (0.23 cyc/deg; visual angle: 18.3 deg) moving upward or downward at 1, 3, and 6 deg/sec for 60 sec. Vertical optokinetic nystagmus (OKN) was monitored. In task B, patients (n=8) and control subjects (n=8) viewed similar spatial frequency gratings (visual angle: 40.7 degs; 0.5, 0.2, 0.08 cyc/deg) which moved at 4, 10, and 16 deg/sec for 60 sec. In task C, five control subjects, with induced vestibular nystagmus, viewed a grating (0.2 cyc/deg; visual acuity: 28.5 deg), moving upward for 40 sec. In all three tasks, after adaptation with the moving grating, subjects viewed the then static grating and reported the duration and direction of the MAE. One CN patient and eight control subjects reported MABs at all three test velocities in task A. When patients exhibited OKN, the gain was close to one, as in the control group. In task B, seven of the eight patients and all of the control subjects had MABs at the faster adaptation velocities. CN patients had less MAEs at an adaptation velocity of 4 deg/sec and when MAEs were observed, the duration of the illusory motion was reduced by approximately 48%. Control subjects, with induced vestibular nystagmus, reported MAEs at 4 deg/sec (task C). These findings indicate that nystagmus cannot be the only factor accounting for the suppression of motion perception and suggest that compensatory mechanisms used to avoid oscillopsia contribute to the differences found between the groups.

Adaptation, Ocular↗

Monocular occlusion cues alter the influence of terminator motion in the barber pole phenomenon.

The influence of monocular occlusion cues on the perceived direction of motion of barber pole patterns is examined. Unlike previous studies that have emphasized the importance of binocular disparity, we find that monocular cues strongly influence the perceived motion direction and can even override binocular depth cues. The difference in motion bias for occluders with and without disparity cues is relatively small. Additionally, although 'T-junctions' aligned with occluders are particularly important, they are not strictly necessary for creating a change in motion perception. Finally, the amount of motion bias differs for several stimulus configurations, suggesting that the extrinsic/intrinsic classification of terminators is not all-or-none.

Contrast Sensitivity↗