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PubMed2006

Directional motion contrast sensitivity in developmental dyslexia.

The present study compared the perception of visual motion in two dyslexia classification schemes; the [Boder, E. (1973). Developmental dyslexia: a diagnostic approach based on three atypical reading-spelling patterns. Developmental Medicine and Child Neurology, 15, 663-687.] dyseidetic, dysphonetic and mixed subgroups and [Williams, M. J., Stuart, G. W., Castles, A., & McAnally, K. I. (2003). Contrast sensitivity in subgroups of developmental dyslexia. Vision Research, 43, 467-477.] surface, phonological and mixed subgroups by measuring the contrast sensitivity for drifting gratings at three spatial frequencies (1.0, 4.0, and 8.0 c/deg) and five drift velocities (0.75, 3.0, 6.0, 12.0, and 18.0 cyc/s) in a sample of 32 children with dyslexia and 32 matched normal readers. The findings show that there were no differences in motion direction perception between normal readers and the group with dyslexia when dyslexia was taken as a homogeneous group. Motion direction perception was found to be intact in the dyseidetic and surface dyslexia subgroups and significantly lowered in both mixed dyslexia subgroups. The one inconsistency in the findings was that motion direction perception was significantly lowered in the [Boder, E. (1973). Developmental dyslexia: a diagnostic approach based on three atypical reading-spelling patterns. Developmental Medicine and Child Neurology, 15, 663-687.] dysphonetic subgroup and intact in the [Williams, M. J., Stuart, G. W., Castles, A., & McAnally, K. I. (2003). Contrast sensitivity in subgroups of developmental dyslexia. Vision Research, 43, 467-477.] phonological subgroup. The findings also provide evidence for the presence of a disorder in sequential and temporal order processing that appears to reflect a difficulty in retaining sequences of non-meaningful auditory and visual stimuli in short-term working memory in children with dyslexia.

Adolescent↗
PubMed1996

Binocular eye movements caused by the perception of three-dimensional structure from motion.

We report that the perception of three-dimensional structure from monocular two-dimensional images changing over time--the kinetic depth effect (KDE)--can evoke binocular eye movements consistent with a three-dimensional percept. We used a monocular KDE stimulus that induced a vivid perception of a rigid three-dimensional sphere rotating in space. The gaze directions of both eyes were measured while observers pursued the motion of a patch on the surface of the perceived sphere as it went through a complete revolution. We found that the eyes converged when the patch was perceived on the front surface of the KDE sphere and diverged when the patch was perceived in the back. The pattern, magnitude and dynamics of binocular eye movements observed in the KDE experiment resembled those obtained when subjects viewed binocularly a light-emitting diode (LED) rotating in space and to the responses obtained with a dynamic stereogram simulating a rotating random dot sphere. Thus, the perception of three-dimensional structure from motion, stereopsis, or motion and stereopsis combined, were effective in guiding binocular eye movements.

Convergence, Ocular↗
PubMed2003

Physiological evidence of interaction of first- and second-order motion processes in the human visual system: a magnetoencephalographic study.

Humans have several mechanisms for the visual perception of motion, including one that is luminance-based (first-order) and another that is luminance-independent (second-order). Recent psychophysical studies have suggested that significant interaction occurs between these two neural processes. We investigated whether such interactions are represented as neural activity measured by magnetoencephalography (MEG). The second-order motion of a drifting sinusoidal grating, which is defined by the speed of the dot motion, did not generate a response. Apparent motion (AM) of the square area, defined by the speed of randomly moving dots, evoked a magnetic response whose latency and amplitude changed with the distance that the area moved (a second-order characteristic), though the response properties were significantly different from those for the first-order AM. AM, defined by both first- and second-order attributes, evoked an MEG response and the latencies and the amplitudes were distributed between those for the first- and second-order motions. The cortical source of the response was estimated to be around MT+. The results show a distinct difference in the neural processing of the second-order motion that cannot be explained by the difference in visibility, and they indicate that the interaction of the neural processes underlying first- and second-order motion detection occurs before the MEG response. Our study provides the first physiological evidence of a neural interaction between the two types of early motion detection.

Adult↗
PubMed1998

[Changes in proprioceptive capacities of the shoulder joint in ventral shoulder instability. A comparative study before and after arthroscopic labrum refixation].

Measurements of movement sense determined by threshold levels for the perception of motion of the shoulder were performed in 10 patients with unilateral posttraumatic shoulder instabilities, in 30 patients who underwent arthroscopic labrum repair for recurrent anterior shoulder instability, and in 15 age-related controls. In patients with anterior shoulder instabilities threshold levels for the perception of motion were higher. In addition, movement sense measurements revealed a marked, but time dependent improve of proprioceptive abilities in patients who underwent arthroscopic labrum repair. While in the shoulders of patients with an postoperative period shorter than 18 months elevated threshold levels for the perception of motion still could be observed, after a postoperative period of 18 moths or more movement sense was not different from normal, uninjured shoulders. In conclusion, our study gives evidence for a proprioceptive deficit with anterior shoulder instability which improves significantly after arthroscopic labrum repair. The restitution of proprioceptive abilities, however, seems to be a time dependent process.

Adult↗
PubMed1990

The color-opponent and broad-band channels of the primate visual system.

Physiological, anatomical and psychophysical studies have identified several parallel channels of information processing in the primate visual system. Two of these, the color-opponent and the broad-band channels, originate in the retina and remain in part segregated through several higher cortical stations. To improve understanding of their function, recent studies have examined the visual capacities of monkeys following selective disruption of these channels. Color vision, fine- but not coarse-form vision and stereopsis are severely impaired in the absence of the color-opponent channel, whereas motion and flicker perception are impaired at high but not low temporal frequencies in the absence of the broad-band channel. The results suggest that the color-opponent channel extends the range of vision in the spatial and wavelength domains, and that the broad-band channel extends it in the temporal domain. Lesion studies also indicate that these channels must reach higher cortical centers through extrastriate regions other than just area V4 and the middle temporal area, and that the analysis performed by these two regions cannot be uniquely identified with specific visual capacities.

Animals↗
PubMed2004

Illusory motion reversal is caused by rivalry, not by perceptual snapshots of the visual field.

In stroboscopic conditions--such as motion pictures--rotating objects may appear to rotate in the reverse direction due to under-sampling (aliasing). A seemingly similar phenomenon occurs in constant sunlight, which has been taken as evidence that the visual system processes discrete "snapshots" of the outside world. But if snapshots are indeed taken of the visual field, then when a rotating drum appears to transiently reverse direction, its mirror image should always appeared to reverse direction simultaneously. Contrary to this hypothesis, we found that when observers watched a rotating drum and its mirror image, almost all illusory motion reversals occurred for only one image at a time. This result indicates that the motion reversal illusion cannot be explained by snapshots of the visual field. The same result is found when the two images are presented within one visual hemifield, further ruling out the possibility that discrete sampling of the visual field occurs separately in each hemisphere. The frequency distribution of illusory reversal durations approximates a gamma distribution, suggesting perceptual rivalry as a better explanation for illusory motion reversal. After adaptation of motion detectors coding for the correct direction, the activity of motion-sensitive neurons coding for motion in the reverse direction may intermittently become dominant and drive the perception of motion.

Humans↗
PubMed2005

Attenuation of perceived motion smear during the vestibulo-ocular reflex.

Previous studies indicated that less motion smear is perceived when a physically stationary target is presented during voluntary eye movements than when similar retinal-image motion occurs during steady fixation. In this study, we assessed whether the perception of motion smear is attenuated also during the involuntary vestibulo-ocular reflex (VOR). Normal observers matched the length of perceived smear in two experimental conditions that were designed to produce similar trajectories of retinal image motion. In the fixation condition, a small bright target was presented for a duration of 50-200 ms in rightward or leftward motion, while the observer remained stationary and maintained fixation. In the VOR condition, the target moved along with the observer, who underwent full-body rotation around a vertical axis in darkness. Horizontal eye movement recordings during VOR trials allowed us to calculate the velocity of retinal image motion on each VOR trial. The principal result was that the extent of perceived motion smear was significantly less during VOR than fixation trials, particularly for target durations of 100 ms or longer. These findings support the conclusion that extra-retinal signals during the involuntary VOR contribute to a reduction of perceived motion smear.

Analysis of Variance↗
PubMed2002

Shifts in perceived position of flashed stimuli by illusory object motion.

Moving stimuli cause the position of flashed stimuli to appear shifted in the direction of motion (position capture). To examine whether position capture depends on low-level motion interactions or perception of integrated object motion, we employed a slit-view display. Two line-drawn diamonds translated horizontally in opposite directions, one above and one below the fixation cross, either behind an occluding surface with a narrow slit or without occluding surface. When the diamonds were in vertical alignment, two vertical bars were flashed, one in the center of each diamond. In the slit-view condition, the diamonds were visible through a 4-, 2-, or 1-pixel vertical slit; the width of the flashed bars always matched the width of the slit. Even though the horizontal component of physical motion was greatly reduced or absent in the slit-view conditions, observers perceived diamonds moving behind the occluding surface. Furthermore, the position of the flashed bar was captured by the moving diamonds such that each bar appeared shifted in the direction of perceived motion. We conclude that the position capture reported here has a component based on high-level motion processing that is responsible for dynamically integrating object motion and shape.

Analysis of Variance↗
PubMed1999

Encoding of motion in real time by the fly visual system.

Direction-selective cells in the fly visual system that have large receptive fields play a decisive role in encoding the time-dependent optic flow the animal encounters during locomotion. Recent experiments on the computations performed by these cells have highlighted the significance of dendritic integration and have addressed the role of spikes versus graded membrane potential changes in encoding optic flow information. It is becoming increasingly clear that the way optic flow is encoded in real time is constrained both by the computational needs of the animal in visually guided behaviour as well as by the specific properties of the underlying neuronal hardware.

Animals↗
PubMed1996

The wagon wheel illusion in movies and reality.

Wheels turning in the movies or in other forms of stroboscopic presentation often appear to be rotating backward. Remarkably, a similar illusion is also seen in continuous light. The occurrence of this perception in the absence of intermittent illumination suggests that we normally see motion, as in movies, by processing a series of visual episodes.

Eye Movements↗
PubMed2004

The influence of motion-defined form on the perception of spatially-defined form.

It is well established that the visual system is sensitive to the global structure--or "form"--of objects defined exclusively by spatial or motion cues, but it remains unclear how form perception combines spatial and motion cues if these are presented concurrently. In the present study, we introduce a novel class of stimuli where spatial-form and motion-form can be superimposed and manipulated independently. In both the spatial and motion domains, global structure consisted of radial-frequency (RF) contours defined by a virtual circle of Gabor elements whose positions and/or drift speeds were sinusoidally modulated at a specified frequency of polar angle. The first two experiments revealed that observers encode the global structure of spatial-RF and motion-RF contours presented in isolation. In a third experiment, observers detected a spatial-RF modulation superimposed on a motion-RF pedestal of identical radial frequency: results showed little facilitation at low pedestal amplitudes but significant masking at higher pedestal amplitudes, especially if the RF modulations of test and pedestal were in anti-phase. Additional experiments demonstrated that masking of the spatial-RF test is abolished if the global structure of the motion-RF pedestal is altered or destroyed while local motion cues are preserved. We argue these results cannot be explained by local neural interactions between spatial and motion cues and propose instead that data reflect higher-level interactions between separate visual pathways encoding spatial-form and motion-form.

Cues↗