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PubMed1998

[Visual perception of movement. A normative study].

BACKGROUND: A battery of tests has been developed to better define the variety of defects which can occur in the process of visual perception of motion. METHODS: The tests assessed the perception of 1) coherent motion, in each of the four cardinal directions; (2) form from motion; (3) flow in depth; and (4) motion of a target moving in depth, within or without an optic flow surround. A normative study was conducted with 34 subjects, 21 to 69 years of age. RESULTS: Recognition of form from motion was better with upwards than with downwards motion. Perception of motion in depth was better with backward than forwards motion. The presence of an optic flow altered the perception of a motion in depth. CONCLUSION: The recognition of form from motion demonstrated an asymmetry in threshold between the upward and downward movements. This asymmetry did not occur with global coherent motion, thus reflecting the variety of mechanisms involved in the visual process of motion. Moreover, alteration of perception of motion in depth within an optic flow reflected background effect.

Adult↗
PubMed1990

Global cooperativity of the short-range process in apparent movement: evidence obtained with contour-containing stimuli.

Previous research has demonstrated that the short-range process in apparent movement, as studied with random-dot cinematograms, exhibits global cooperativity; that is, computations performed by local elements interact nonlinearly and are pooled. Other research using displays containing extended contours has implicated the short-range process, but has never demonstrated global cooperativity. In the first of four experiments, it was shown that under certain conditions of presentation, a short-range motion percept exhibiting apparent global cooperativity can be obtained when collections of randomly located contours are rotated about the center of a display, despite the fact that the displacement of peripheral contours falls outside the normal limit of the short-range process. Experiments 2-4 were conducted to provide further evidence that the observed motion is short-range (i.e., it can be disrupted by illuminating the interstimulus interval or with dichoptic viewing) and that the percept is globally cooperative (i.e., masking the center of the display, where separations between corresponding elements across frames are smallest, results in a decline in the frequency of reports of the short-range percept). Control observations suggest that the effect produced with masks was not due to a decrease in the number of elements in the display. The argument that the display exhibits a short-range process with global cooperativity is further developed.

Adult↗
PubMed2005

Individuation of visual objects over time.

How does an observer decide that a particular object viewed at one time is actually the same object as one viewed at a different time? We explored this question using an experimental task in which an observer views two objects as they simultaneously approach an occluder, disappear behind the occluder, and re-emerge from behind the occluder, having switched paths. In this situation the observer either sees both objects continue straight behind the occluder (called "streaming") or sees them collide with each other and switch directions ("bouncing"). This task has been studied in the literature on motion perception, where interest has centered on manipulating spatiotemporal aspects of the motion paths (e.g. velocity, acceleration). Here we instead focus on featural properties (size, luminance, and shape) of the objects. We studied the way degrees and types of featural dissimilarity between the two objects influence the percept of bouncing vs. streaming. When there is no featural difference, the preference for straight motion paths dominates, and streaming is usually seen. But when featural differences increase, the preponderance of bounce responses increases. That is, subjects prefer the motion trajectory in which each continuously existing individual object trajectory contains minimal featural change. Under this model, the data reveal in detail exactly what magnitudes of each type of featural change subjects implicitly regard as reasonably consistent with a continuously existing object. This suggests a simple mathematical definition of "individual object:" an object is a path through feature-trajectory space that minimizes feature change, or, more succinctly, an object is a geodesic in Mahalanobis feature space.

Bayes Theorem↗
PubMed2004

Contrast-reversing global-motion stimuli reveal local interactions between first- and second-order motion signals.

Motion perception appears to be mediated by, at least, two systems: a first-order and a second-order system. To investigate the degree of interaction between these systems, we used a contrast-reversing global-motion stimulus in which the signal dots reverse their contrast polarity as they move. In response to such a stimulus, fullwave-rectifying second-order units would signal motion in the displacement direction and first-order units would signal motion in the opposite direction (reverse-phi motion). If these signals were of equal strength, then any inhibitory interaction between them would lead to motion nulling. Such a situation would account for the failure to perceive coherent motion with such a stimulus in a previous study [Vis. Res. 34 (1994) 2849]. In order to test for this possibility we manipulated the stimulus in order to reduce the strength of the second-order response relative to the first-order response. This was achieved by: decreasing dot contrast; increasing stimulus eccentricity; and increasing dot speed. These manipulations resulted in an increase in the perception of (first-order mediated) reverse-phi motion. We conclude that interaction between first- and second-order motion signals occur at the local-motion-pooling level.

Adaptation, Ocular↗
PubMed1997

The size and number of plaid blobs mediate the misperception of type-II plaid direction.

The misperceived direction of type-II plaids has posed a problem for the intersection of constraints (IOC) model of two-dimensional motion perception. Alais et al. (1994, Vision Research, 34, 1823-1834) examined the perceived direction of type-II plaids and concluded that in addition to the direction signalled by the IOC process, a monocular mechanism signalling the motion of plaid features (blobs) is also involved in plaid perception. It was shown that the prominence of this monocular signal in plaid direction judgements depended on several variables, and the notion of blob "optimality" was introduced. This explained the more veridical direction of "optimal" blob plaids in terms of their more effectively activating the proposed feature-sensitive motion mechanism. One distinction between "optimal" and "non-optimal" blob plaids is their different component spatial frequencies, which necessarily entails a difference in the number and size of the blobs and thus raises potential confounds, since both the nature of the blobs and the components differ, which might affect the postulated blob mechanism and/or the IOC process. In the present paper, by offsetting changes in spatial frequency with changes in aperture size so that blob number is held constant, we examine whether differences in sheer blob number or size can alter perceived type-II plaid direction. The results reveal effects of both blob number and blob size, and their implications for the underlying mechanism are considered. Alternative accounts of the results in terms of the IOC model or revisions of it cannot explain the data. Comparison of monocular and binocular conditions adds further systematic evidence in support of the monocularity of the feature-sensitive motion mechanism.

Analysis of Variance↗
PubMed1978

Two dimensionality of the correspondence process in apparent motion.

A fundamental process underlying motion perception is the matching of corresponding elements in different views. In this correspondence process spatial separation between elements plays a major role. The relevant separation is shown by the current study to be the two-dimensional, uninterpreted distance, a finding that has an implication to the level at which the correspondence process is carried out. The current findings are compared with earlier results concerning 'optimality' of apparent motion to conclude that optimality cannot serve as a measure for the correspondence strength.

Depth Perception↗
PubMed1995

Perspectives on the role of afferent signals in control of motor neuroprostheses.

K.O. Johnson reviews the architecture and low level neural mechanisms by which the external environment is transduced and encoded into the neural system, summarizing work that correlates neurophysiological and psychophysical testing with isolation of sensory components. The slowly adapting Type I afferent system is responsible for form and texture perception; the rapidly adapting afferent system is responsible for motion perception; and the Pacinian corpuscle system is responsible for vibratory sensation. R.R. Riso reviews the current level of understanding of the major factors to be considered in the design of a functional neuromuscular stimulation (FNS) grasp controller that uses cutaneous sensory feedback to detect slip. The elegant natural control scheme that matches the ratio of grip and lift forces to frictional conditions provides a model for implementing a slip-based control algorithm. D. Popović discusses the possible use of recordings from more proximal peripheral nerves to determine needed information for synthesis of locomotion. The discussion is illustrated with an animal model where rule-based closed-loop control is used for the ankle joint during treadmill locomotion. Neural signals from the tibial and superficial peroneal nerves were employed to substitute for missing afferent input from cutaneous and proprioceptive sensors. The feasibility of more invasive intraneural electrodes for distinguishing sensory from motor information in mixed nerves is considered. M. Koris raises surgical and functional issues relevant to developing clinical FNS systems. C. Van Doren suggests alternative neurophysiological and engineering approaches.

Afferent Pathways↗
PubMed1991

The spacing illusion: a spatial aperture problem?

A geometrical illusion in which the horizontal spacing between adjacent parallel lines in a row is underestimated when the lines are tilted away from vertical in a chevron configuration was investigated in two experiments. The perceived spacing was found to decrease as the tilt angle increased, consistent with the idea that separation judgements are influenced by the normal spacing between lines ie at right angles to the line orientation. It is proposed that this illusion reveals an analogue in spatial perception to the well-known aperture problem in motion perception. In establishing the separation of nearby or overlapping shapes in an image, the visual system cannot only rely upon the normal separation of contours belonging to each shape (as would be visible through small spatial apertures or receptive fields), since this varies with contour orientation. The system is therefore faced with a spatial aperture problem. The spacing illusion may arise because information usually available to solve the problem is absent in the illusion figure, or it may reflect a bias in favour of the orthogonal, which is adopted in the face of the ambiguity.

Adult↗
PubMed2003

Contribution of middle temporal area to coarse depth discrimination: comparison of neuronal and psychophysical sensitivity.

Recent work suggests that the middle temporal (MT) area contributes to depth perception in addition to its well established roles in motion perception. To determine whether single MT neurons carry disparity signals with sufficient fidelity to account for depth perception, we have compared neuronal and psychophysical sensitivity to disparity while monkeys discriminated between two coarse disparities (near vs far) in the presence of noise. The strength of the visual stimulus was titrated around psychophysical threshold by varying the percentage of binocularly correlated dots in a random dot stereogram. We find that the average MT neuron has sensitivity equal to that of the monkey, as was reported previously for direction discrimination in MT. We further address some important factors that could bias the neuronal/psychophysical sensitivity comparison, including the possibility that monkeys reach a decision before the end of the stimulus presentation. Unlike the predictions of a simple model that uses Poisson spiking statistics, the sensitivity of many MT neurons has little dependence on the time interval over which spikes are counted to compute a neuronal threshold. Thus the response properties of many MT neurons appear to be adapted for rapid discrimination of depth, and we describe how temporal variations in both signal and noise contribute to this effect. We therefore predicted that psychophysical thresholds should exhibit little dependence on viewing duration in our task, and this was confirmed by additional behavioral experiments. Overall, our findings show that MT is well suited to provide sensory signals that form the basis for perceptual judgments of depth.

Action Potentials↗
PubMed1992

Motion sickness and perception: a reappraisal of the sensory conflict approach.

This review examines the role of activity and perceptual learning in motion sickness by means of a survey of the two kinds of recent research relevant to this topic. The first is a body of literature concerned not with motion sickness as such, but with perception of orientation and self-motion under the conditions of 'sensory conflict' which are thought to provoke motion sickness. The second consists of investigations into the prediction and prevention of motion sickness itself. A major weakness is identified in the methodologies employed in both types of research: namely, a neglect of the way in which responses to unusual and disorienting environments, whether nauseogenic or not, may be affected by the activities, skills and strategies of the perceiver. New directions are outlined for future research into immediate reactions and longer-term adaptation to such environments.

Female↗
PubMed1992

Linear vection in the central visual field facilitated by kinetic depth cues.

Illusory self-motion (vection) is thought to be determined by motion in the peripheral visual field, whereas stimulation of more central retinal areas results in object-motion perception. Recent data suggest that vection can be produced by stimulation of the central visual field provided it is configured as a more distant surface. In this study vection strength (tracking speed, onset latency, and the percentage of trials where vection was experienced) and the direction of self-motion produced by displays moving in the central visual field were investigated. Apparent depth, introduced by using kinetic occlusion information, influenced vection strength. Central displays perceived to be in the background elicited stronger vection than identical displays appearing in the foreground. Further, increasing the eccentricity of these displays from the central retina diminished vection strength. If the central and peripheral displays were moved in opposite directions, vection strength was unaffected, and the direction of vection was determined by motion of the central display on almost half of the trials when the centre was far. Near centres produced fewer centre-consistent responses. A complete understanding of linear vection requires that factors such as display size, retinal locus, and apparent depth plane are considered.

Adult↗
PubMed2004

Imaging cortical correlates of illusion in early visual cortex.

Exploring visual illusions reveals fundamental principles of cortical processing. Illusory motion perception of non-moving stimuli was described almost a century ago by Gestalt psychologists. However, the underlying neuronal mechanisms remain unknown. To explore cortical mechanisms underlying the 'line-motion' illusion, we used real-time optical imaging, which is highly sensitive to subthreshold activity. We examined, in the visual cortex of the anaesthetized cat, responses to five stimuli: a stationary small square and a long bar; a moving square; a drawn-out bar; and the well-known line-motion illusion, a stationary square briefly preceding a long stationary bar presentation. Whereas flashing the bar alone evoked the expected localized, short latency and high amplitude activity patterns, presenting a square 60-100 ms before a bar induced the dynamic activity patterns resembling that of fast movement. The preceding square, even though physically non-moving, created gradually propagating subthreshold cortical activity that must contribute to illusory motion, because it was indistinguishable from cortical representations of real motion in this area. These findings demonstrate the effect of spatio-temporal patterns of subthreshold synaptic potentials on cortical processing and the shaping of perception.

Animals↗
PubMed1999

Saccadic suppression precedes visual motion analysis.

There is now good evidence that perception of motion is strongly suppressed during saccades (rapid shifts of gaze), presumably to blunt the disturbing sense of motion that saccades would otherwise elicit. Other aspects of vision, such as contrast detection of high-frequency or equiluminant gratings, are virtually unaffected by saccades [1] [2] [3] [4] [5]. This has led to the suggestion that saccades may suppress selectively the magnocellular pathway (which is strongly implicated in motion perception), leaving the parvocellular pathway unaffected [5] [6]. Here, we investigate the neural level at which perception of motion is suppressed. We used a simple technique in which an impression of motion is generated from only two frames, allowing precise control over the stimulus [7] [8]. One frame has a certain fixed contrast, whereas the contrast of the other (the test frame) is varied to determine the threshold for motion discrimination (that is, the lowest test-frame contrast level at which the direction of motion can be correctly guessed). Contrast thresholds of the test depended strongly and non-monotonically on the contrast of the fixed-contrast frame, with a minimum at medium contrast. To study the effect of saccadic suppression, we triggered the two-frame sequence by a voluntary saccade. Thresholds during saccades increased in a way that suggested that saccadic suppression precedes motion analysis: when the test frame was first in the motion sequence there was a general depression of sensitivity, whereas when it was second, the contrast response curve was shifted to a higher contrast range, sometimes even resulting in higher sensitivity than without a saccade. The dependence on presentation order suggests that saccadic suppression occurs at an early stage of visual processing, on the single frames themselves rather than on the combined motion signal. As motion detection itself is thought to occur at an early stage, saccadic suppression must take place at a very early phenomenon.

Humans↗
PubMed1999

Visual processing and dyslexia.

Magnocellular-pathway deficits have been hypothesized to be responsible for the problems experienced by dyslexic individuals in reading. However, research has yet to provide a detailed account of the consequences of these deficits or to identify the behavioural link between them and reading disabilities. The aim of the present study was to determine the potential consequences of the magnocellular-pathway deficits for dyslexics in a comprehensive range of visual tasks. Dyslexics and nondyslexics were compared on their ability to (i) perform vernier-acuity and orientation-acuity tasks; (ii) perceive motion by using a range of measures common in the psychophysical literature (Dmin, Dmax, and global coherence); and (iii) perceive shapes presented in random-dot stereograms at a range of disparity pedestals, thereby dissociating stereopsis from vergence control. The results indicated no significant differences in performance between the dyslexic and nondyslexic subjects in terms of the visual-acuity measures. In general, dyslexics performed relatively poorly on measures of motion perception and stereopsis, although when considered individually some of the dyslexics performed better than some of the controls. The poor performance of the dyslexics in the stereo-gram tasks was attributable to a subgroup of dyslexics who also appeared to have severe difficulty with the motion-coherence task. These data are consistent with previous evidence that some dyslexics may have deficits within the magnocellular visual pathway.

Adolescent↗
PubMed1994

Full-wave and half-wave processes in second-order motion and texture.

A theory of human second-order motion perception is proposed and further applied to the discrimination of texture slant. The computational algorithms for deriving the direction of left-right motion from a sequence of images are equivalent to the algorithms for deriving the direction of slant (e.g. from top left to bottom right or top right to bottom left) in a single 2D image. There is a broad range of phenomena for which Fourier analysis of the image plus a few simple rules gives a good account of human perception. The problem with this first-order analysis is that there exists a broad class of 'microbalanced' stimuli in which the motion or slant is completely obvious to human subjects but is invisible to first-order analysis. Microbalanced stimuli require second-order analysis which consists of non-linear preprocessing (spatiotemporal filtering followed by rectification of the input signal) before standard motion or slant analysis. To determine whether the second-order rectification is half-wave or full-wave, we construct two special microbalanced stimulus types: 'half-wave stimuli' whose motion (or texture slant) is interpretable by a half-wave rectifying system but not by full-wave or a first-order (Fourier) analysis and 'full-wave stimuli' which are interpretable only after full-wave rectification. Such experiments show that second-order texture-slant perception utilizes both half-wave and full-wave processes, second-order motion-direction discrimination depends predominantly on full-wave rectification and second-order spatial interactions such as lateral contrast-contrast inhibition and second-order Mach bands are exclusively full-wave.

Algorithms↗
PubMed1982

The perception of biological motion by human infants.

When a small number of lights are placed on the limbs and joints of a moving human (or animal), the motions of the lights (biological motion) are sufficient to enable adult observers to perceive immediately the activity of the human. This perception of biological motion has been hypothesized to be an intrinsic capacity of the visual system. The results of this experiment, which demonstrate that infants 4 to 6 months of age exhibit a preference for biological motion patterns, support that hypothesis.

Age Factors↗
PubMed1990

Static depth cues do affect the perceived direction of motion.

Models of motion perception usually assume that the visual system references spatial displacements to retinal coordinates, and not to three-dimensional coordinates recovered by a parallel process. The present studies investigated whether moving elements viewed in the context of a static random-dot stereogram could lead to the appearance of motion in depth. Observers judged the velocity of a monocular element translating horizontally in the stereo context as 'same as' or 'different to' that of a standard. Based on velocity constancy, if there was apparent motion in depth, the relative velocity judgments would yield a predictable pattern of errors. The first experiment compared two stereo contexts: a sloped surface versus a fronto-parallel plane at zero disparity. The results indicated an overall increase in the perceived velocity of the element moving in the sloped surface context. A similar pattern of results was found when surfaces differing in incline were compared. Experiment 2 explored the case of fronto-parallel planes at crossed and uncrossed disparities. Here depth differences did not systematically affect observers' judgments. It was concluded that in some cases motion analysis can be affected by three-dimensional disparity information and not by angular displacement alone.

Acceleration↗