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PubMed1990

Motion mechanisms have only limited access to form information.

We investigate the roles of spatial frequency content, flicker and higher-order elements of form ("features") in the generation of motion percepts. These cues are separated through the use of dynamic visual stimuli based on stochastic textures. Flicker alone and spatial frequency content alone suffice to generate a strong motion percept, but higher-order elements of form alone generate a much weaker motion percept. Thus, even for achromatic stimuli, all pattern information is not equally available for motion processing. Furthermore, higher-order form information, which by itself does not provide a strong cue to motion, is shown to interact with other visual information to facilitate determination of direction of motion.

Adult↗
PubMed2003

Direction-selective motion blindness after unilateral posterior brain damage.

Motion blindness (MB) is defined as the selective disturbance of visual motion perception despite intact perception of other features of the visual scene. MB is characterized by a pandirectional deficit of motion direction discrimination and is assumed to result from damage to the visual motion pathway, especially area MT/V5. However, the most characteristic feature of primate MT/V5 neurons is not their motion selectivity but their preference for one direction of motion (direction selectivity), which changes incrementally at neighbouring columns. In addition to this microscopic directional organization, studies in nonhuman and human primates suggest that single directions of motion are also coded at a more macroscopic level. We thus hypothesized that if MB in humans results from damage to direction-selective neurons in the visual motion pathway, posterior brain damage might cause MB which is direction selective, not pandirectional. The present study investigated motion direction discrimination in patients with posterior unilateral brain damage and determined separate psychophysical thresholds for the four cardinal directions. In addition, we analysed whether the direction of erroneous motion perception (i.e. the perception of right motion for upward motion) was random or showed a directional bias. We report three principal findings. First, motion direction discrimination was severely impaired in one or two directions while it was normal in the other directions. This constituted direction-selective MB. Second, MB was characterized not only by a quantitative direction-selective increase in psychophysical thresholds but also by a qualitative impairment of perceiving motion direction systematically in wrong directions. Both findings suggest that the cortical modules specialized for the perception of a single direction of motion might be larger than previously thought. Third, lesion analysis showed that unilateral damage, not only the human homologue of MT/V5 but also to parieto-occipital cortex, leads to MB.

Adult↗
PubMed2000

Auditory agnosia and auditory spatial deficits following left hemispheric lesions: evidence for distinct processing pathways.

Auditory recognition and auditory spatial functions were studied in four patients with circumscribed left hemispheric lesions. Patient FD was severely deficient in recognition of environmental sounds but normal in auditory localisation and auditory motion perception. The lesion included the left superior, middle and inferior temporal gyri and lateral auditory areas (as identified in previous anatomical studies), but spared Heschl's gyrus, the acoustic radiation and the thalamus. Patient SD had the same profile as FD, with deficient recognition of environmental sounds but normal auditory localisation and motion perception. The lesion comprised the postero-inferior part of the frontal convexity and the anterior third of the temporal lobe; data from non-human primates indicate that the latter are interconnected with lateral auditory areas. Patient MA was deficient in recognition of environmental sounds, auditory localisation and auditory motion perception, confirming that auditory spatial functions can be disturbed by left unilateral damage; the lesion involved the supratemporal region as well as the temporal, postero-inferior frontal and antero-inferior parietal convexities. Patient CZ was severely deficient in auditory motion perception and partially deficient in auditory localisation, but normal in recognition of environmental sounds; the lesion involved large parts of the parieto-frontal convexity and the supratemporal region. We propose that auditory information is processed in the human auditory cortex along two distinct pathways, one lateral devoted to auditory recognition and one medial and posterior devoted to auditory spatial functions.

Aged↗
PubMed2004

Central inhibition ability modulates attention-induced motion blindness.

Impaired motion perception can be induced in normal observers in a rapid serial visual presentation task. Essential for this effect is the presence of motion distractors prior to the motion target, and we proposed that this attention-induced motion blindness results from high-level inhibition produced by the distractors. To investigate this, we compared the extent of the attention-induced motion blindness effect with performance on central inhibition tasks: Stroop colour naming and negative priming. A negative correlation between Stroop interference and motion performance reflected that low Stroop scores, indicative of strong inhibition ability, was associated with more severe impairments in motion perception. This association could not be explained by individual differences in fluid intelligence, task switching or response speed. Negative priming was not specifically associated with attention-induced motion blindness. The results confirm that attention can modulate motion perception and suggest that the processes involved may be shared with high-level cognitive abilities.

Adult↗
PubMed1995

Restricted ability to recover three-dimensional global motion from one-dimensional motion signals: psychophysical observations.

We tested human ability to recover the 3D structure and motion information from time-varying images where only 1D motion cues were available. Under these conditions, observers exhibit poor performance in discriminating between two perpendicular axes of rotation, or discriminating between rigid and non-rigid 3D motion. This behavior of the visual system is to be contrasted with the good depth from motion performance exhibited when 2D motion cues are given in the image, as was found previously in numerous studies, and also in the work presented here. In a related paper, we suggest a theoretical framework in which to understand this differential performance on the basis of the two types of motion cues (1D vs 2D). Our findings are consistent with those of previous studies of frontoparallel motion, where it was shown that in many cases, the 1D cues alone were not integrated by the visual system into the correct global motion percept. This accumulating evidence suggests that oriented (1D) motion detectors alone cannot account for observed human performance of global motion perception, and that the role of units such as point or endpoint detectors should be studied further.

Cues↗
PubMed2005

Impaired visual recognition of biological motion in schizophrenia.

BACKGROUND: Motion perception deficits have been suggested to be an important feature of schizophrenia but the behavioral consequences of such deficits are unknown. Biological motion refers to the movements generated by living beings. The human visual system rapidly and effortlessly detects and extracts socially relevant information from biological motion. A deficit in biological motion perception may have significant consequences for detecting and interpreting social information. METHODS: Schizophrenia patients and matched healthy controls were tested on two visual tasks: recognition of human activity portrayed in point-light animations (biological motion task) and a perceptual control task involving detection of a grouped figure against the background noise (global-form task). Both tasks required detection of a global form against background noise but only the biological motion task required the extraction of motion-related information. RESULTS: Schizophrenia patients performed as well as the controls in the global-form task, but were significantly impaired on the biological motion task. In addition, deficits in biological motion perception correlated with impaired social functioning as measured by the Zigler social competence scale [Zigler, E., Levine, J. (1981). Premorbid competence in schizophrenia: what is being measured? Journal of Consulting and Clinical Psychology, 49, 96-105.]. CONCLUSION: The deficit in biological motion processing, which may be related to the previously documented deficit in global motion processing, could contribute to abnormal social functioning in schizophrenia.

Adult↗
PubMed1998

A nonlinear chromatic motion mechanism.

Previous research has demonstrated two categorically distinct mechanisms mediating apparent motion of kinematograms composed of eccentricity-confined, randomly placed Gabor micropatterns: a quasi-linear mechanism operating for high micropattern densities and short time separations, and a nonlinear mechanism operating at low micropattern densities or longer time separations. Here we compare the performance of these two mechanisms using color (isoluminant) and luminance-defined stimuli. When these stimuli are defined only by their color contrast, the response of the quasi-linear mechanism is severely impaired, while the nonlinear mechanism remains fully operative. This result further strengthens the dichotomy between the two kinds of motion perception, and suggests that when color vision supports motion perception it does so primarily, or perhaps entirely, via a nonlinear mechanism.

Color Perception↗
PubMed1992

Perception of motion and position relative to the earth. An overview.

Results of the five experiments are consistent with the following generalizations. Canal-mediated turn perception (pitch, roll, or yaw) in earth-horizontal or earth-vertical plane, is suppressed in direct relationship to the magnitude of a linear acceleration vector lying in the plane of a responding canal when the magnitude of the linear vector is constant or increasing and when its direction is either fixed or rotating in the same direction as the concomitant canal signal. Canal-mediated turn perception (pitch, roll, or yaw) is not suppressed by a coplanar linear vector that is counterrotating relative to the canal signal. Change in perceived attitude (pitch, roll, or yaw) is very sluggish in the absence of concordant canal information; attitude change may not be an immediate otolith-mediated perceptual event but a slowly developing perception dependent upon cognitive appreciation of an immediate otolith angular position signal. Otolith phasic neural units, unreinforced by appropriate canal signals, may contribute more to a brief linear velocity component in perception than to rate of attitude change. Otolith-mediated attitude perception within a given earth-vertical plane can be distorted by strong coplanar angular velocity canal information. Once distorted, return to veridical attitude perception can be gradual because, in the absence of complimentary canal or visual information, recovery is dependent upon relatively slow cognitive appreciation of a prevailing otolith position signal. Several attractive hypotheses relating to the dynamics of attitude perception can only be tested by substantially more data on the dynamics of spatial orientation perception. Most of our objectives cannot be achieved without models that yield valid prediction of the dynamics of spatial orientation perception. All of the observations in these experiments were carried out in darkness, or, in the simulated catapult experiment, without external visual reference. Various forms of visual information will change the dynamics of spatial orientation perception. My discussion has been limited to consideration of the vestibular system, as though the canal and otolith systems completely controlled the dynamics of spatial orientation perceptions. Obviously other partners in the dynamics of postural control, including vision, proprioception, and expectation, must be included in this challenging field of research. Dedication to stereotyped ideas about objectivity in the 20th century has hindered advancement of knowledge on the dynamics of spatial orientation perception relative to rate of progress achieved by several scientists of the 18th and 19th centuries, who provided word pictures of perceived motions and tilts along with descriptions of the motions that engendered the pictures.(ABSTRACT TRUNCATED AT 400 WORDS)

Gravitation↗
PubMed1998

Is human motion detection subserved by a single or multiple channel mechanism?

Two recent versions of a single channel model of motion perception have had impressive success in explaining direction discrimination by human observers for spatially filtered noise images in two-flash apparent motion. It has been argued that the dramatic breakdown in motion perception which occurs when one image in the two-flash sequence is low-pass filtered can be explained only by a single channel model. We show that neither version of the single channel model which has been proposed can explain performance for noise images chosen to provide comparable stimulation in the spatial channels known to subserve human vision. A multi-channel model of motion perception has little difficulty in explaining these results.

Discrimination, Psychological↗
PubMed1996

Thresholds for detection of motion direction during passive lateral whole-body acceleration in normal subjects and patients with bilateral loss of labyrinthine function.

To investigate the effect of velocity, acceleration, and gradient of acceleration on self-motion perception, thresholds for detection of direction of whole-body interaural acceleration were determined for various stimulus profiles. For acceleration steps, acceleration thresholds at 67% correct detection of motion direction were similar for eight normals (mean 4.84 cm/s2 (range 2.9-6.3), peak gradient = 22 cm/s2) and five labyrinthine-defective subjects (mean 5.65 cm/s2 (4.85-6.6), peak gradient = 25 cm/s2). Velocity thresholds were 7.93 cm/s for a proportion of correct responses of 73% for normals and 9.67 cm/s for 69% of correct detection for avestibular subjects. For linear and parabolic accelerations, high intersubject variability was observed both among nine normals and three labyrinthine-defective subjects. Mean normal and avestibular subjects' acceleration thresholds for 74% of correct responses were respectively 12.1 cm/s2 (7.3-20.4) and 16.4 cm/s2 (13.2-20) for a ramp with gradient of acceleration = 2.8 cm/s3, 19.2 cm/ s2 (10.4-35.3) and 28.2 cm/s2 (21.4-32.8) for a ramp with gradient = 7.9 cm/s3 and 16.7 cm/s2 (10.5-25) and 20.6 cm/s2 (18.4-24.2) for a parabola with second derivative = 1.52 cm/s4. The corresponding velocity thresholds for normals were 21.2 cm/s (5.2-50.3), 22.0 cm/s (7-56.6), and 22.2 cm/s (9.5-43.7). The lowest thresholds were obtained for acceleration steps indicating that a high acceleration gradient facilitates motion perception. For linear and parabolic accelerations, motion perception seemed to follow an integration of acceleration, but a high intersubject variability was observed. For all stimuli, the range of thresholds for normals and avestibular subjects overlapped showing that detection of motion was not a sole prerogative of the otoliths but could also be performed using somatosensory cues.

Adult↗
PubMed1988

A computational theory for the perception of coherent visual motion.

When we see motion, our perception of how one image feature moves depends on the behaviour of other features nearby. In particular, the Gestaltists proposed the law of shared common fate, in which features tend to be perceived as moving together, that is, coherently. Recent psychophysical findings, such as the cooperativity of the motion system and motion capture, support this law. Computationally, coherence is a sensible assumption, because if two features are close then they probably belong to the same object and thus tend to move together. Moreover, the measurement of local motion may be inaccurate and so the integration of motion information over large areas may help to improve the performance. Present theories of visual motion, however, do not account fully for these coherent motion percepts. We propose here a theory that does account for these phenomena and also provides a solution to the aperture problem, where the local information in the image flow is insufficient to specify the motion uniquely.

Humans↗
PubMed1990

Impairment of vertical motion detection and downgaze palsy due to rostral midbrain infarction.

We present two cases with acute onset of vertical gaze palsy, mainly consisting of impaired downgaze and apraxia of downward head movements, together with neuropsychological deficits (hypersomnia, impaired attention and disorders of memory and affective control). CT and MRI revealed bilateral post-ischaemic lesions in the dorsomedial thalamus and the mesodiencephalic junction, dorsomedial to the red nucleus, thus being restricted to the territory of the posterior thalamosubthalamic paramedian artery, which includes the region of the rostral interstitial nucleus of the medial longitudinal fascicle as the main premotor nucleus for the generation of vertical saccades. In our patients, oculographic examination with electro-oculography and magnetic search coil recording showed severe impairment of downward more than upward saccades and only minor deficits of vertical pursuit and the vestibulo-ocular reflex. Visual functions were normal, with one exception: a psychophysical test of motion perception revealed a significant deficit in the detection of vertical movements. This could be due to a central adaptive mechanism which, in order to minimize oscillopsia, might elevate thresholds for vertical motion perception in cases of vertical gaze palsy. As an alternative explanation, lesions within the midbrain tegmentum could have damaged subcortical visual pathways involved in motion perception.

Cerebral Infarction↗
PubMed1993

Depth perception in motion parallax and stereokinesis.

Perceived depth in the stereokinetic effect (SKE) illusion and in the monocular derivation of depth from motion parallax were compared. Motion parallax gradients of velocity can be decomposed into 2 components: object- and observer-relative transformations. SKE displays present only the object-relative component. Observers were asked to estimate the magnitude and near-far order of depth in motion parallax and SKE displays. Monocular derivation of depth magnitude from motion parallax is fully accounted for by the perceptual response to the SKE, and observer-relative transformations absent in the SKE are of perceptual utility only as determinants of the near-far signing of perceived sequential depth. The amount of depth and rigidity perceived in motion parallax and SKE displays covaries with the projective size of the stimuli. The monocular derivation of depth from motion is mediated by a perceptual heuristic of which the SKE is symptomatic.

Adult↗
PubMed2002

Colour and luminance interactions in the visual perception of motion.

We sought to determine the extent to which red-green, colour-opponent mechanisms in the human visual system play a role in the perception of drifting luminance-modulated targets. Contrast sensitivity for the directional discrimination of drifting luminance-modulated (yellow-black) test sinusoids was measured following adaptation to isoluminant red-green sinusoids drifting in either the same or opposite direction. When the test and adapt stimuli drifted in the same direction, large sensitivity losses were evident at all test temporal frequencies employed (1-16 Hz). The magnitude of the loss was independent of temporal frequency. When adapt and test stimuli drifted in opposing directions, large sensitivity losses were evident at lower temporal frequencies (1-4 Hz) and declined with increasing temporal frequency. Control studies showed that this temporal-frequency-dependent effect could not reflect the activity of achromatic units. Our results provide evidence that chromatic mechanisms contribute to the perception of luminance-modulated motion targets drifting at speeds of up to at least 32 degrees s(-1). We argue that such mechanisms most probably lie within a parvocellular-dominated cortical visual pathway, sensitive to both chromatic and luminance modulation, but only weakly selective for the direction of stimulus motion.

Adaptation, Ocular↗
PubMed2005

Visual dysfunction in Parkinson disease without dementia.

OBJECTIVE: To determine the profiles of visual dysfunction and their relationship to motor and cognitive dysfunction and to disability in mild to moderate Parkinson disease (PD) without dementia. METHODS: Seventy-six independently living participants with mild to moderate PD and 161 neurologically normal older adults were studied using a comprehensive battery to assess visual acuity, contrast sensitivity (CS), visual speed of processing and attention, spatial and motion perception, visual and verbal memory, visuoconstructional abilities, executive functions, depression, and motor function. RESULTS: Participants with PD scored significantly worse on all tests of vision and cognition compared with normal elderly persons. Reduced CS contributed to deficits on tests of spatial and motion perception and attention in participants with PD. Impairments in visual attention and spatial perception predicted worse cognitive function. Worse performances on tests of visual speed of processing and attention, spatial and motion perception, visual construction, and executive functions correlated with measures of postural instability and gait difficulty (in the Motor section of the Unified Parkinson's Disease Rating Scale). Impairments in motor function, visual memory, mood, and executive functions predicted worse disability as measured by Schwab-England Activities of Daily Living Scale. CONCLUSIONS: Patients with mild to moderate Parkinson disease showed impaired visual perception and cognition compared with elderly control subjects. Visual dysfunction contributes to parkinsonian disability through its influences on cognition and locomotion.

Aged↗
PubMed2005

Spatial and motion integration in children with autism.

Neuropsychological and psychophysical studies report controversial results regarding local-global visual processing and motion perception in autism. Here, we investigate contour integration and motion perception in an accurately diagnosed sample of autistic children, using low-level psychophysical tasks. We measured detection thresholds for a closed chain of Gabor patches, for different values of inter-element distance and we measured coherency thresholds of optic flow motion stimuli. Both experiments show comparable performances between autistics and normal subjects, demonstrating no evidence of early perceptual integration deficits. Some improvement in performance with age is detected in both groups.

Adolescent↗
PubMed2001

Systematic eye movements do not account for the perception of motion during attentive tracking.

It has been suggested that attention can disambiguate stimuli that have equal motion energy in opposite directions (e.g. a counterphasing grating), such that a clear motion direction is perceived. The direction of this movement is determined by the observer and can be changed at will. Assuming that the responses of front-end motion detectors are equal for the two opponent directions, it has been proposed that the unambiguous motion perceived with attentive tracking arises from an independent mechanism that monitors the shifts of attention directed to the moving feature of interest. However, while perceiving motion under attentive tracking conditions, observers often report a strong impression that they are making eye movements. In this study, we investigated whether systematic eye movements are present during attentive tracking and, as a result, could be responsible for the subjective experience of movement. We had observers track an object in smooth motion, apparent motion and ambiguous motion, either with eye movements or with attention. The results show that there are negligible eye movements during attentive tracking, which are neither systematic nor correlated with the stimulus. Given that neither eye movements nor retinal image motion can account for subjectively perceived motion, as well as the absence of any other plausible explanation, we find it tempting evidence for an earlier suggestion that the percept of movement must arise from a specialized mechanism.

Attention↗