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PubMed1992

Properties of cyclopean motion perception.

This study investigated the ability of human observers to discriminate the direction of laterally-moving cyclopean stimuli, in order to assess some of the properties of stereoscopic mechanisms that mediate the perception of cyclopean motion (motion existing at levels of binocular integration). The stimuli were moving grating patterns created from dynamic random-dot stereograms. Experiment 1 showed that duration thresholds for discrimination decrease with velocity; they are not governed by temporal frequency nor a constant spatial displacement. Experiment 2 revealed that discrimination thresholds increase with disparity magnitude, for both the crossed and uncrossed disparity directions equally. Experiment 3 showed that the rate of temporal variation at and above which direction discrimination fails (cyclopean upper limit of temporal resolution) is 8 Hz. Our results indicate that a mechanism for motion perception exists at binocular-integration levels of the visual system, which supports a model of motion perception that posits the existence of first-order and second-order processes.

Depth Perception↗
PubMed1998

Anomalies of motion perception in infantile esotropia.

PURPOSE: To quantify motion sensitivity in patients with infantile esotropia who, as a subgroup, have been previously reported to have abnormal oculomotor control. In addition, to probe abnormal binocular development as a factor underlying abnormal motion perception in infantile esotropia (IE), motion sensitivity was compared among participants with and without stereopsis. METHODS: Monocular sensitivity to leftward and rightward motion was assessed across the horizontal meridian, using partially coherent random dot kinematograms. Participants included 11 observers with IE, 5 observers with acquired esotropia, and 11 observers with normal eye alignment. RESULTS: Participants with IE showed no deficits in motion sensitivity to any visual field locations when motion thresholds were collapsed across direction. However, they showed an abnormal variation in directional anisotropy. Although sensitivity to centripetal motion was superior in both hemifields of control participants and in the temporal hemifields of participants with IE, a centrifugal bias was revealed in the nasal hemifields of IE. Stereoblind observers with acquired esotropia showed a normal centripetal directional anisotropy, whereas binocular observers with acquired esotropia showed directional anisotropy similar to that in the IE group. CONCLUSIONS: Motion perception, like oculomotor function in IE, is characterized by a variation of directional anisotropy for stimuli presented to the nasal hemifields. This finding supports the hypothesis that abnormal oculomotor control and motion perception in IE reflect a common disruption of the visual system. A similar variation of directional sensitivity in patients with acquired esotropia with normal stereopsis suggests that the interruption of binocularity is not the underlying cause of abnormal motion perception in IE.

Adolescent↗
PubMed1996

Directional defects in pursuit and motion perception in humans with unilateral cerebral lesions.

We tested motion perception and smooth pursuit in 26 patients with unilateral cerebral hemispheric lesions. We used random dot cinematograms to test motion direction discrimination. We measured pursuit gain as they followed a predictable sinusoidal target moving horizontally at three different frequencies, and an unpredictable horizontal step-ramp target in the ipsilateral hemi-field. Six patients had defects in motion perception when the targets were moving towards the side of the lesions ('ipsi-directional' defects) and two had bi-directional defects. Motion perception defects occurred with lesions of the junction of Brodmann areas 19 and 37, a putative human homologue of the monkey V5 complex. Seven patients had ipsi-directional pursuit defects, five of whom had damage to the posterior limb of the internal capsule. Only two patients had ipsi-directional defects of both motion perception and sinusoidal smooth pursuit. Four patients had ipsi-directional defects of motion perception alone, and five patients had ipsi-directional pursuit defects alone. The two patients with bi-directional defects in motion perception had normal sinusoidal smooth pursuit. Patients with lesions at the 19/37 junction and defects of motion perception alone had normal pursuit of unpredictable step-ramp targets in the ipsilateral hemi-field. In contrast, patients with ipsi-directional sinusoidal pursuit defects had decreased ipsi-directional and increased contra-directional velocities with step-ramp targets. No patient group had a motion-specific directional defect in saccadic accuracy. We conclude that neither predictable nor unpredictable pursuit is necessarily impaired by lesions of the 19/37 junction that cause ipsi-directional defects of motion perception. These dissociations between smooth pursuit and motion perception provide evidence that the pursuit system operates as an interconnected network with parallel pathways, rather than as a simple sequential hierarchy of cortical areas.

Adult↗
PubMed1998

Bilateral vestibular failure impairs visual motion perception even with the head still.

Visual motion perception of a single object, moving with a constant angular velocity of 40 min of arc/s in four orthogonal directions, was measured in eight patients with chronic bilateral vestibular failure (BVF) with the head stationary. Perception of object motion was more severely impaired for horizontal than for vertical directions and the impairment was more pronounced in the dominant eye than the nondominant eye. Impaired motion perception in patients with BVF is best explained by a central visual mechanism that suppresses oscillopsia due to the involuntary retinal slip caused by the defective vestibulo-ocular reflex (VOR). This mechanism cannot be switched off with the head stationary (inactive VOR) and thus causes a measurable deficit of motion perception.

Adult↗
PubMed1998

Motion evoked brain potentials parallel the consistency of coherent motion perception in humans.

The perception of global coherent motion perception in complex motion patterns containing different direction vectors was investigated. Random dot kinematograms (RDK), plaids and fragmented plaid pattern were presented in which direction vectors of the moving elements were varied. In order to elicit coherent motion perception, all elements were displaced in the same direction (delta0 degrees). In a second condition, fifty percent of the elements were moved diagonally downwards to the left, with the remaining elements moving orthogonally (delta 90 degrees). Simultaneously with psychophysical judgements on the perceived motion direction, visual evoked potentials (VEPs) were recorded at occipital electrode positions. Onset of a global coherent motion was associated with a VEP negativity occurring at about 200 ms. The amplitude of this component was clearly reduced when local ambiguous signals could not be integrated to produce the perception of global coherent motion.

Adult↗
PubMed2000

A transient deficit of motion perception in human.

We studied the motion perception abilities in a young adult, SF, who had her right occipito-temporal cortices resected to treat epilepsy. Following resection, SF showed transient deficits of both first- and second-order motion perception that recovered to normal within weeks. Previous human studies have shown either first- or second n order motion deficits that have lasted months or years after cerebral damage. SF also showed a transient defect in processing of shape-from-motion with normal perception of shape from non-motion cues. Furthermore, she showed greatly increased reaction times for a mental rotation task, but not for a lexical decision task. The nature and quick recovery of the deficits in SF resembles the transient motion perception deficit observed in monkey following ibotenic acid lesions, and provides additional evidence that humans possess specialized cortical areas subserving similar motion perception functions.

Adult↗
PubMed1993

Motion perception in glaucoma.

PURPOSE: This study was performed to investigate motion perception in patients with glaucoma. METHODS: A random dot motion test was used to measure three aspects of central motion perception: minimum displacement threshold (Dmin), maximum displacement threshold (Dmax), and coherence threshold (signal to noise). Motion perception was assessed in 15 patients with primary open-angle glaucoma, 23 low-risk patients in whom glaucoma was suspected, and 24 age-matched normal subjects. RESULTS: Central motion perception was significantly impaired in patients with glaucoma; in particular, the Dmin was nearly twice that for the normal subjects (glaucoma mean, -0.27 +/- 0.24 log minutes of arc; normal mean, -0.56 +/- 0.13 log minutes of arc; F = 21.79, P < 0.001). Furthermore, Dmin values fell outside the normal range in 10 of the 15 patients with glaucoma, despite normal visual acuity and normal foveal perimetric thresholds. Coherence thresholds and Dmax did not discriminate between patients with glaucoma and normal subjects. Dmin was not correlated with any indices of perimetric sensitivity, and none of the tests of motion perception showed any abnormalities in patients in whom glaucoma was suspected. CONCLUSIONS: Central motion perception can be affected in glaucoma and may reflect preferential damage to larger retinal ganglion cells. Future work will measure Dmin in a larger population of patients with suspected glaucoma and those with glaucoma, and investigate peripheral motion perception in glaucoma.

Adult↗
PubMed2006

A model of biological motion perception from configural form cues.

Biological motion perception is the compelling ability of the visual system to perceive complex human movements effortlessly and within a fraction of a second. Recent neuroimaging and neurophysiological studies have revealed that the visual perception of biological motion activates a widespread network of brain areas. The superior temporal sulcus has a crucial role within this network. The roles of other areas are less clear. We present a computational model based on neurally plausible assumptions to elucidate the contributions of motion and form signals to biological motion perception and the computations in the underlying brain network. The model simulates receptive fields for images of the static human body, as found by neuroimaging studies, and temporally integrates their responses by leaky integrator neurons. The model reveals a high correlation to data obtained by neurophysiological, neuroimaging, and psychophysical studies.

Adult↗
PubMed2006

Motion perception in the ageing visual system: minimum motion, motion coherence, and speed discrimination thresholds.

We aimed to address two issues: first, to describe how the perception of motion differs in elderly observers as compared to younger ones; and, second, to see if these changes in motion perception could be accounted for by the known changes in the ability of elderly observers to detect patterns (as indexed via contrast sensitivity). The lower threshold of motion, motion coherence, and speed discrimination were measured, alongside contrast sensitivity, in a group of thirty-two older (mean age 61.5 years) and thirty-two younger (mean age 23.2 years) subjects. The older observers showed losses in their ability to detect slow motions as indexed via the lower threshold of motion for random-dot patterns and for gratings of a range of spatial frequencies. They also were impaired on a test of motion coherence, but only for stimuli of a slow to medium speed, whereas faster speeds showed no decline with age. Finally, at all speeds tested the older observers required greater differences in speed in order to discriminate between patterns moving at different speeds. The pattern of losses on motion perception tasks was not predicted by the deficits of the older groups, such as loss of detection thresholds for high spatial and/or temporal frequencies. It is concluded that these hypotheses do not provide an adequate account of the data, and therefore that the losses occurring with age are complex and probably are a result of the loss of several types of cell.

Adolescent↗
PubMed1988

Motion perceptions induced by off-vertical axis rotation (OVAR) at small angles of tilt.

Off-vertical axis rotation in darkness induces a perception of body motion which lasts as long as rotation continues. Perceived body motion is the combination of two simultaneous displacements. The most easily perceived is a translation without rotation along a conical path, at the frequency of the actual rotation. Meanwhile, the subjects feel as if they were always facing towards the same direction. The summit of the cone is generally below the head, from the waist to below the feet, and subjects have a sense of progression in the direction opposite to actual spinning. Some subjects feel, on the contrary, the summit of the cone above their heads, and the progression in the direction of spinning. Subjects also perceived another body motion, although it was faint for some of them. It consists of a rotation at low velocity in the same direction as progression along the cone. The axis of the cone is perceived as slowly rotating along a larger cone. These motion perceptions increase with tilt angle and rotation velocity. They probably result from the analysis by the Central Nervous System of the acceleration acting on the otoliths. The perceived trajectory would be reconstructed from estimates of gravity, and kinematic variables such as head translational acceleration and velocity, and head rotational velocity. The same variables would account for OVAR-induced nystagmus. Motion sickness would result from the impossibility of reconstructing a consistent body movement from most sets of values of these variables.

Adult↗
PubMed1992

Cortical dynamics of visual motion perception: short-range and long-range apparent motion.

This article describes further evidence for a new neural network theory of biological motion perception. The theory clarifies why parallel streams V1----V2, V1----MT, and V1----V2----MT exist for static form and motion form processing among the areas V1, V2, and MT of visual cortex. The theory suggests that the static form system (Static BCS) generates emergent boundary segmentations whose outputs are insensitive to direction-of-contrast and to direction-of-motion, whereas the motion form system (Motion BCS) generates emergent boundary segmentations whose outputs are insensitive to direction-of-contrast but sensitive to direction-of-motion. The theory is used to explain classical and recent data about short-range and long-range apparent motion percepts that have not yet been explained by alternative models. These data include beta motion, split motion, gamma motion and reverse-contrast gamma motion, delta motion, and visual inertia. Also included are the transition from group motion to element motion in response to a Ternus display as the interstimulus interval (ISI) decreases; group motion in response to a reverse-contrast Ternus display even at short ISIs; speed-up of motion velocity as interflash distance increases or flash duration decreases; dependence of the transition from element motion to group motion on stimulus duration and size, various classical dependencies between flash duration, spatial separation, ISI, and motion threshold known as Korte's laws; dependence of motion strength on stimulus orientation and spatial frequency; short-range and long-range form-color interactions; and binocular interactions of flashes to different eyes.

Attention↗
PubMed1994

Transparent motion perception as detection of unbalanced motion signals. II. Physiology.

We investigated how the primate visual system solves the difficult problem of representing multiple motion vectors in the same part of the visual space--the problem of motion transparency. In the preceding companion article we reported that displays with locally well-balanced motion signals in opposite directions are perceptually nontransparent (i.e., one does not see two coherent moving surfaces) and that transparent displays always contain locally unbalanced motion signals. This is exemplified by our paired and unpaired dot patterns. Although both types of stimuli contain two sets of dots moving in opposite directions, the former is locally well balanced and appears like flicker while the latter gives a perception of two transparent surfaces. In this article we report our physiological recordings from areas V1 and MT of behaving monkeys, comparing single-cell responses to the paired and the unpaired dot patterns. Although a small proportion of directionally selective V1 cells responded differently to the two types of patterns, the average V1 responses could not reliably distinguish between the paired and the unpaired stimuli. A large fraction of MT cells, on the other hand, responded significantly better to the unpaired dot patterns than to the paired ones. Furthermore, the average response of all MT cells to the unpaired dot patterns was significantly higher than that to the paired dot patterns. These results demonstrate a neural correlate of the perceptual transparency at the level of MT. On the other hand, V1 cells do not generally discriminate between the transparent and nontransparent stimuli, indicating that V1 activity is not well correlated with the perception of motion transparency. Our results are consistent with a two-stage model for motion processing: the first stage measures local motion and the second stage introduces suppression if different directions of motion are present at a local region of the visual field. The first stage is located primarily in V1 and the second stage primarily in MT. Finally, we found a strong and negative correlation between the degree of the opponent-direction suppression of MT cells and their responses to flicker noise stimuli. This result suggests that one of the fundamental roles of the opponent-direction suppression in MT is noise reduction.

Animals↗
PubMed2003

Accuracy and precision of binocular 3-D motion perception.

In principle, information for 3-D motion perception is provided by the differences in position and motion between left- and right-eye images of the world. It is known that observers can precisely judge between different 3-D motion trajectories, but the accuracy of binocular 3-D motion perception has not been studied. The authors measured the accuracy of 3-D motion perception. In 4 different tasks, observers were inaccurate, overestimating trajectory angle, despite consistently choosing similar angles (high precision). Errors did not vary consistently with target distance, as would be expected had inaccuracy been due to misestimates of viewing distance. Observers appeared to rely strongly on the lateral position of the target, almost to the exclusion of the use of depth information. For the present tasks, these data suggest that neither an accurate estimate of 3-D motion direction nor one of passing distance can be obtained using only binocular cues to motion in depth. ((c) 2003 APA, all rights reserved)

Discrimination, Psychological↗
PubMed1997

The characteristics of interaction between color and motion perception in primary open angle glaucoma.

PURPOSE: To investigate the characteristics of interaction between color and motion perception in primary open angle glaucoma (POAG) and measure motion perception of B, G and R cones, thus find a more sensitive method to diagnose the visual nerve damage in POAG. METHODS: Motion perceptions of B, G and R cones were isolated by blue, green and red vertical line stimulus displayed on the yellow, purple and blue background respectively, then measured the displacement threshold and flicking threshold of motion perception from each cones in POAG, and compared it with the age-match normals. RESULTS: The displacement threshold and flicking threshold of motion perception from B, G and R cones were all damaged in POAG compared with the normals, and the motion perception of G and B cones was deficits more obviously than the R cones. CONCLUSION: These findings support the suggestion that color provides an input to human motion perception. Magnocellular and parvocellular pathway may be significantly damaged in POAG, which indicates, that the combination of Motion Perception and color testing may reveal preclinical visual nerve damage in early POAG.

Adult↗
PubMed1983

Global and local precedence: selective attention in form and motion perception.

This study explores the perception of stimuli at two levels: local parts and the wholes that comprise these parts. Previous research has produced contradictory results. Some studies (e.g., Pomerantz & Sager, 1975) show local precedence, in which the local parts are more difficult to ignore in selective attention tasks. Other studies (e.g., Navon, 1977) have shown the opposite effect, global precedence. The present five experiments trace the causes of this discrepancy by exploring the effects of the relative discriminabilities of the local and global levels of the stimuli and the differences between two different measures of selective attention, namely, Stroop-type interference (attributable to incongruity on the irrelevant dimension) and Garner-type interference (attributable to variability on the irrelevant dimension). The experiments also examine whether the precedence effects previously examined in form perception generalize to motion perception. The results show that (a) some cases of global precedence are due solely to the greater perceptual discriminability of the global level and thus demonstrate only that more discriminable stimuli are harder to ignore; (b) instances of both local and global precedence can be demonstrated for certain types of stimuli, even when the discriminabilities of their local and global levels have been equated; and (c) the Stroop and Garner measures of selective attention are not equivalent but instead measure different types of interference. In addition, a distinction is made between two fundamentally different types of part-whole relationships that exist in visual configurations, one based only on the positions of the parts (Type P) and one based also on the nature of the parts (Type N). Previous research has focused on Type P, which appears to be irrelevant to the broader questions of Gestalt and top-down effects in perception. It is concluded that bona fide cases of both local and global precedence have been amply documented but that no general theory can account for why or when these effects will appear until we better understand both the nature of part-whole relationships and the perceptual processes that are tapped by different measures of selective attention.

Adult↗
PubMed2001

Cortical responses to object-motion and visually-induced self-motion perception.

We investigated the spatiotemporal cortical dynamics during the perception of object-motion and visually-induced self-motion perception in six normal subjects, using a 143-channel neuromagnetometer. Object-motion specific tasks evoked early transient activity over the right temporooccipital cortex, while self-motion perception, or vection, additionally was followed by sustained bilateral activity in the temporoparietal area. The specific signal distributions suggest to represent the different perceptual modes of object-motion and self-motion sensation.

Adult↗
PubMed1999

Motion parallel to line orientation: disambiguation of motion percepts.

Four experiments demonstrate that lines indicating path of movement can generate rotational percepts in a multistable motion display that usually produces only horizontal or vertical motion percepts. The properties of the path-of-movement lines are predicted by a neural-network theory of visual perception. Experimental results validate the theory's predictions by demonstrating that movement of the display elements seems to follow an increasing luminance gradient in lines but not bars, and that illusory contours have similar effects. Experimental results also demonstrate that, in a choice between movement along lines drawn parallel or orthogonal to possible motion paths, observers more often see movement along the lines parallel to the motion path. These results suggest modifications to current computational and neurophysiological theories of motion perception.

Computer Graphics↗