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PubMed2005

Psychophysical estimation of speed discrimination. I. Methodology.

Thresholds were assessed for a speed discrimination task with a pair of luminance-defined drifting gratings. The design and results of a series of experiments dealing in general with speed discrimination are described. Results show that for a speed discrimination task using drifting gratings, simultaneous presentation of the pair of gratings (spatially separated) was preferred over sequential presentation (temporally separated) in order to minimize the effects of eye movements and tracking. An interstimulus interval of at least 1000 ms was necessary to prevent motion aftereffects on subsequently viewed stimuli. For the two reference speeds tested of 2 and 8 deg/s using identical spatial frequency or randomizing spatial frequency for the pair of gratings did not affect speed discrimination thresholds. Implementing a staircase method of estimating thresholds was preferred over the method of constant stimuli or the method of limits. The results of these experiments were used to define the methodology for an investigation of aging and motion perception. These results will be of interest and use to psychophysicists designing and implementing speed discrimination paradigms.

Adaptation, Ocular↗
PubMed1990

Dissociation of short- and long-range apparent motion in visual search.

The visual search paradigm was used in four experiments to investigate apparent motion perception. The addition of distractor items led to a linear increase in reaction time under long-range (LR) conditions (greater than 35 min of arc displacement), whereas reaction time was independent of displays size under short-range (SR) conditions (less than 18 min of arc). Although clear performance differences were obtained, Ss had difficulty in distinguishing between the two types of apparent motion displays when asked to make such judgments (Experiment 2). Experiments 3 and 4 explored some variables that may constrain the search process. Search times under LR conditions were reduced when some of the distractors were stationary or the motion of the distractors was homogeneous. Form and motion were found to be separable, whereas color and motion were not. Varying the color (and brightness) interfered with the processing of motion information.

Adult↗
PubMed2000

The emergence of visual objects in space-time.

It is natural to think that in perceiving dynamic scenes, vision takes a series of snapshots. Motion perception can ensue when the snapshots are different. The snapshot metaphor suggests two questions: (i) How does the visual system put together elements within each snapshot to form objects? This is the spatial grouping problem. (ii) When the snapshots are different, how does the visual system know which element in one snapshot corresponds to which element in the next? This is the temporal grouping problem. The snapshot metaphor is a caricature of the dominant model in the field-the sequential model-according to which spatial and temporal grouping are independent. The model we propose here is an interactive model, according to which the two grouping mechanisms are not separable. Currently, the experiments that support the interactive model are not conclusive because they use stimuli that are excessively specialized. To overcome this weakness, we created a new type of stimulus-spatiotemporal dot lattices-which allow us to independently manipulate the strength of spatial and temporal groupings. For these stimuli, sequential models make one fundamental assumption: if the spatial configuration of the stimulus remains constant, the perception of spatial grouping cannot be affected by manipulations of the temporal configuration of the stimulus. Our data are inconsistent with this assumption.

Humans↗
PubMed1999

How does noise influence the estimation of speed?

Local motion signals have to be combined in space and time, to yield a coherent motion percept as it is involved in a variety of visual tasks. This combination necessarily means to trade-off between loosing spatio-temporal resolution by pooling local signals and maintaining perceptually significant segmentation between them. When signals are pooled to detect the presence of coherent motion in large amounts of random noise, the question raised is how the noise affects the perceived quality, in particular speed, of the coherent motion. Is there an analogy to the well-known reduction in the perceived speed of moving gratings at low contrast? Using a two-interval forced-choice procedure, we have investigated the assessment of speed in random-dot kinematograms containing different proportions of noise. Under the conditions investigated, there is no strong reduction of perceived speed with increasing noise, as long as coherence levels remain well above the thresholds for directional judgements. This basic result, which could suggest considerable but not perfect segregation of signal and noise motion components in the pooling process leading to speed estimation, is discussed in relation to a model that is designed to decode speed from a population of elementary motion detectors (EMDs) of the correlation type. A strategy to estimate speed from a set of EMDs with a variety of spatio-temporal tuning does not only provide a velocity predictor unambiguous with the spatial structure of the stimulus, but also is largely independent of noise.

Adult↗
PubMed2000

A geometric view on early and middle level visual coding.

As opposed to dealing with the geometry of objects in the 3D world, this paper considers the geometry of the visual input itself, i.e. the geometry of the spatio-temporal hypersurface defined by image intensity as a function of two spatial coordinates and time. The results show how the Riemann curvature tensor of this hypersurface represents speed and direction of motion, and thereby allows to predict global motion percepts and properties of MT neurons. It is argued that important aspects of early and middle level visual coding may be understood as resulting from basic geometric processing of the spatio-temporal visual input. Finally, applications show that the approach can improve the computation of motion.

Animals↗
PubMed2001

Pursuit compensation during self-motion.

The pattern of motion in the retinal image during self-motion contains information about the person's movement. Pursuit eye movements perturb the pattern of retinal-image motion, complicating the problem of self-motion perception. A question of considerable current interest is the relative importance of retinal and extra-retinal signals in compensating for these effects of pursuit on the retinal image. We addressed this question by examining the effect of prior motion stimuli on self-motion judgments during pursuit. Observers viewed 300 ms random-dot displays simulating forward self-motion during pursuit to the right or to the left; at the end of each display a probe appeared and observers judged whether they would pass left or right of it. The display was preceded by a 300 ms dot pattern that was either stationary or moved in the same direction as, or opposite to, the eye movement. This prior motion stimulus had a large effect on self-motion judgments when the simulated scene was a frontoparallel wall (experiment 1), but not when it was a three-dimensional (3-D) scene (experiment 2). Corresponding simulated-pursuit conditions controlled for purely retinal motion aftereffects, implying that the effect in experiment 1 is mediated by an interaction between retinal and extra-retinal signals. In experiment 3, we examined self-motion judgments with respect to a 3-D scene with mixtures of real and simulated pursuit. When real and simulated pursuits were in opposite directions, performance was determined by the total amount of pursuit-related retinal motion, consistent with an extra-retinal 'trigger' signal that facilitates the action of a retinally based pursuit-compensation mechanism. However, results of experiment 1 without a prior motion stimulus imply that extra-retinal signals are more informative when retinal information is lacking. We conclude that the relative importance of retinal and extra-retinal signals for pursuit compensation varies with the informativeness of the retinal motion pattern, at least for short durations. Our results provide partial explanations for a number of findings in the literature on perception of self-motion and motion in the frontal plane.

Depth Perception↗
PubMed2004

Abnormal global processing along the dorsal visual pathway in autism: a possible mechanism for weak visuospatial coherence?

Frith and Happe (Frith, U., & Happe, F. (1994). Autism: Beyond theory of mind. Cognition, 50, 115-132) argue that individuals with autism exhibit 'weak central coherence': an inability to integrate elements of information into coherent wholes. Some authors have speculated that a high-level impairment might be present in the dorsal visual pathway in autism, and furthermore, that this might account for weak central coherence, at least at the visuospatial level. We assessed the integrity of the dorsal visual pathway in children diagnosed with an autism spectrum disorder (ASD), and in typically developing children, using two visual tasks, one examining functioning at higher levels of the dorsal cortical stream (Global Dot Motion (GDM)), and the other assessing lower-level dorsal stream functioning (Flicker Contrast Sensitivity (FCS)). Central coherence was tested using the Children's Embedded Figures Test (CEFT). Relative to the typically developing children, the children with ASD had shorter CEFT latencies and higher GDM thresholds but equivalent FCS thresholds. Additionally, CEFT latencies were inversely related to GDM thresholds in the ASD group. These outcomes indicate that the elevated global motion thresholds in autism are the result of high-level impairments in dorsal cortical regions. Weak visuospatial coherence in autism may be in the form of abnormal cooperative mechanisms in extra-striate cortical areas, which might contribute to differential performance when processing stimuli as Gestalts, including both dynamic (i.e., global motion perception) and static (i.e., disembedding performance) stimuli.

Autistic Disorder↗
PubMed1993

Isolating the effect of one-dimensional motion signals on the perceived direction of moving two-dimensional objects.

A considerable body of evidence suggests the existence of a two-stage mechanism for the detection of global motion. In the first stage the motion of elongated contours is extracted and then at the second stage these one-dimensional (1D) motion signals are combined. What is the nature of the computation carried out in combining the 1D motion signals towards forming a global motion percept? We devised a set of stimuli that differentiate between different possible computations. In particular, they distinguish between a velocity-space construction (such as intersection of constraints) and a linear computation such as vector averaging. In addition, these stimuli do not contain two-dimensional (2D) motion signals such as line intersections, that allow unambiguous determination of global velocity. Stimuli were presented in uncrossed disparity relative to the aperture through which they were presented, to reduce the effect of line terminator motion. We found that subjects are unable to detect the veridical global direction of motion for these stimuli. Instead, they perceive the stimulus pattern to be moving in a direction which reflects the average of its 1D motion components. Our results suggest that the visual system is not equipped with a mechanism implementing a velocity-space computation of global motion.

Humans↗
PubMed2006

Cortical locus of coherent motion deficits in deaf poor readers.

Samar and Parasnis [Samar, V. J., & Parasnis, I. (2005). Dorsal stream deficits suggest hidden dyslexia among deaf poor readers: correlated evidence from reduced perceptual speed and elevated coherent motion detection thresholds. Brain and Cognition, 58, 300-311.] reported that correlated measures of coherent motion detection and perceptual speed predicted reading comprehension in deaf young adults. Because deficits in coherent motion detection have been associated with dyslexia in the hearing population, and because coherent motion detection is strongly dependent on extrastriate cortical area MT, these results are consistent with the claim that hidden dyslexia occurs within the deaf population and is associated with deficits in MT. However, coherent motion detection can also be influenced by subcortical deficits in both magnocellular and parvocellular pathways. To confirm the putative cortical locus of coherent motion perception deficits, we measured contrast thresholds for detecting the direction of movement of drifting sine wave gratings in the same participant group as [Samar, V. J., & Parasnis, I. (2005). Dorsal stream deficits suggest hidden dyslexia among deaf poor readers: correlated evidence from reduced perceptual speed and elevated coherent motion detection thresholds. Brain and Cognition, 58, 300-311.], under stimulus conditions that selectively biased for input from the subcortical magnocellular and parvocellular pathways, respectively. Contrast thresholds were not related to reading comprehension performance under either the magnocellular or parvocellular conditions. Furthermore, the previously reported correlations among reading comprehension, coherent motion thresholds, and perceptual speed remained significant even after contrast thresholds and non-verbal IQ were controlled in partial correlation analyses. In addition, coherent motion detection thresholds were found to correlate specifically with a reading-IQ discrepancy score, one commonly used indicator of dyslexia. These results provide direct psychophysical evidence that the previously reported deficit in coherent motion detection in deaf poor readers does not involve subcortical pathway deficits, but rather is associated with a cortical deficit likely involving area MT. They also strengthen the argument for the existence of hidden dyslexia in the deaf adult population.

Adolescent↗
PubMed2005

Expectation of sensory stimulation modulates brain activation during visual motion stimulation.

The differential effects of visual hemifield motion stimulation during fixation of a stationary target were compared under two conditions: fixation straight ahead without any further instructions and fixation straight ahead with attention shifted to the "dark hemifield." Data from nine right-handed volunteers revealed that striate and extrastriate right hemispheric visual areas exhibited larger activations during left hemifield motion stimulation when attention was shifted to the right dark hemifield. Montreal Neurological Institute (MNI) coordinates (26, -98, -4) of the additional clusters activated in the latter condition corresponded best to the kinetic occipital region, which is known to process both shape and motion information, and to parts of area V3 posterior to V3A, which has been shown repeatedly to mediate motion perception. A simple computational model of transhemispheric visuovisual interaction is proposed. The basic mechanism of this model is a central predictor formed by a feedback loop that detects a mismatch between input to the two hemispheres. Predicted stimulation is then compared with the actual input. If the sensed motion of a visual hemifield is larger than the predicted net motion in the model, activation of the respective neural population is increased; conversely, a smaller actual motion causes less activation.

Adult↗
PubMed1990

Spatiotemporal contrast sensitivity differs in normal aging and Parkinson's disease.

We measured contrast sensitivity for static and laterally drifting vertical gratings in 12 young adults, 7 normal elderly adults, and 8 patients with Parkinson's disease (PD). We compared static and motion contrast sensitivity for spatial frequencies of 0.25, 1, and 4 cycles per degree (cpd), and temporal frequencies of 1, 3, and 9 Hz. Results show that normal aging leads to a reduction of motion sensitivity for the spatial frequency of 0.25 cpd. Compared with elderly controls, PD patients do not present specific abnormalities in this domain. However, for spatial frequencies of 1 and 4 cpd and temporal frequencies of 1 and 3 Hz, motion sensitivity is worse than static sensitivity in PD patients and not in elderly controls. These findings suggest a specific deficit of motion perception in PD, and possible dopaminergic involvement in the control of visuospatial behavior.

Adult↗
PubMed2003

Directional anisotropies reveal a functional segregation of visual motion processing for perception and action.

Human exhibits an anisotropy in direction perception: discrimination is superior when motion is around horizontal or vertical rather than diagonal axes. In contrast to the consistent directional anisotropy in perception, we found only small idiosyncratic anisotropies in smooth pursuit eye movements, a motor action requiring accurate discrimination of visual motion direction. Both pursuit and perceptual direction discrimination rely on signals from the middle temporal visual area (MT), yet analysis of multiple measures of MT neuronal responses in the macaque failed to provide evidence of a directional anisotropy. We conclude that MT represents different motion directions uniformly, and subsequent processing creates a directional anisotropy in pathways unique to perception. Our data support the hypothesis that, at least for visual motion, perception and action are guided by inputs from separate sensory streams. The directional anisotropy of perception appears to originate after the two streams have segregated and downstream from area MT.

Animals↗
PubMed1994

Temporal integration of random dot apparent motion information in human central vision.

Human motion perception is assumed to be functionally described by an array of bi-local detectors feeding later, higher order computational stages. Using this model as a guide, improvement of spatio-temporal displacement sensitivity by temporal integration (summation) was measured in human central vision using random dot pattern apparent-motion stimuli. Our results agree with previous experiments with regard to improvement of maximum perceivable spatial displacement but show that contrary to previous results the minimum perceivable spatial displacement can be improved in a similar manner. Furthermore, stimulus duration is a more accurate predictor of sensitivity than the number of frames in the stimulus over a wide range of stimulus parameter values. Finally, our results indicate that temporal tuning of motion detectors is inversely related to the size of the spatial pattern displacement.

Contrast Sensitivity↗
PubMed1988

The perception of an optical flow projected on the ground surface.

In most experiments in which the importance of visual control on postural stability is studied, optical stimuli attached to vertical surfaces are used. Analyses of long-term standing readjustments generally involve back-and-forth movements of a visual scene or its projection on vertical circular screens. In a natural environment, however, visual information is largely available from the ground. The aim of the experiment reported was to assess the effect of a flow pattern simulating an open outdoor setting on motion perception and postural control. Subjects were presented with an optical texture projected onto the ground. Periods of motionless texture alternated with equivalent durations of unidirectional flows. The change of position of the subject's centre of gravity over time was recorded on a force platform. Results show that the direction of body sway corresponded with that of texture motion. Important aftereffects, as shown in linear vection experiments, were also observed. However, the latency of postural responses was much shorter than with prolonged unidirectional flows produced in other locations of the visual environment. The hypothesis of an ecological specificity of the flows perceived on the ground during terrestrial displacements is discussed.

Adult↗
PubMed2005

Collision judgment of objects approaching the head.

Recent investigations have indicated that human perception of the trajectory of objects approaching in the horizontal plane is precise but biased away from straight ahead. This is remarkable because it could mean that subjects perceive objects that approach on a collision course as missing the head. Approach within the horizontal plane through the eyes and the fixation point (the plane of regard) is special, as general motions will also have a component of motion perpendicular to the plane of regard. Thus, we investigated three-dimensional motion perception in the vicinity of the head, including vertical components. Subjects judged whether an object that moved in the mid-sagittal plane was going to hit below or above a well-known reference point on the face like the center of the chin or the forehead (perceptual task). Tactile and proprioceptive information about the reference point significantly improved precision. Precision did not change with distance of the approaching target or with fixation direction. Bias was virtually absent for these vertical motions. When subjects pointed with their index finger to the perceived location of impact on their face (visuo-motor task), they overestimated (1.7 cm) the horizontal eccentricity of the point of impact (pointing task). Vertical bias, however, was again virtually absent. Interestingly, when trajectories intersected the plane of regard, higher precision was observed in the perceptual task regardless of the other conditions. In contrast, neither bias nor precision of the pointing task changed significantly when the trajectories intersected the plane of regard. When asked to point to the location where a trajectory intersected the plane of regard, subjects overestimated the depth component of this intersection location by about 3 cm. The absence of perceptual and pointing bias in the vertical direction in contrast to the clear horizontal bias suggests that different (combinations of) cues are used to judge these components of the trajectory of an approaching object. The results of our perceptual task suggest a role for somatosensory signals in the visual judgment of impending impact.

Analysis of Variance↗
PubMed1990

Coherence determines speed discrimination.

The visual system must determine which elements in a scene to regard as parts of a single object and which to regard as different objects. We can create stimuli that are ambiguous, ie consistent with more than one interpretation, and ask in what situations the stimulus elements are interpreted as part of a single object and when they are interpreted as multiple objects. The ambiguous stimuli in this study were moving plaid patterns--the sum of two drifting gratings with different orientations. Observers may see a rigid coherent plaid object moving in one direction, or may see two gratings moving in different directions sliding over one another. When the gratings have similar contrasts they appear to cohere and only the plaid speed is perceptually available; when the gratings have different contrasts they appear to slide and only the speeds of the gratings are perceived. Coherence thus determines what speed information is passed to higher stages of motion processing. A two-stage model of plaid motion perception is presented which agrees with the model proposed by Adelson and Movshon and extends it, detailing the relationship between coherence and speed discrimination.

Acceleration↗
PubMed2004

Adaptive temporal integration of motion in direction-selective neurons in macaque visual cortex.

Direction-selective neurons in the primary visual cortex (V1) and the extrastriate motion area MT/V5 constitute a critical channel that links early cortical mechanisms of spatiotemporal integration to downstream signals that underlie motion perception. We studied how temporal integration in direction-selective cells depends on speed, spatial frequency (SF), and contrast using randomly moving sinusoidal gratings and spike-triggered average (STA) analysis. The window of temporal integration revealed by the STAs varied substantially with stimulus parameters, extending farther back in time for slow motion, high SF, and low contrast. At low speeds and high SF, STA peaks were larger, indicating that a single spike often conveyed more information about the stimulus under conditions in which the mean firing rate was very low. The observed trends were similar in V1 and MT and offer a physiological correlate for a large body of psychophysical data on temporal integration. We applied the same visual stimuli to a model of motion detection based on oriented linear filters (a motion energy model) that incorporated an integrate-and-fire mechanism and found that it did not account for the neuronal data. Our results show that cortical motion processing in V1 and in MT is highly nonlinear and stimulus dependent. They cast considerable doubt on the ability of simple oriented filter models to account for the output of direction-selective neurons in a general manner. Finally, they suggest that spike rate tuning functions may miss important aspects of the neural coding of motion for stimulus conditions that evoke low firing rates.

Action Potentials↗
PubMed1994

Detection of temporal order of noise-like luminance functions.

We study the capacities of human observers to time order light sources that emit dynamic noise, identical for the different light sources, except for an adjustable delay. There is a range of temporal delays for which human observers are perfectly able to perform this task, using the direction of the motion percept that is evoked by the stimulus as a cue. An optimal delay between light sources at which the observers are most robust against any deterioration of the stimulus is defined. We claim that optimal delays (15-25 msec) correspond to the time delay of a putative Reichardt correlation mechanism in human motion vision. Contrary to the ability of human observers to sense temporal correlations in noise sequences, observers are totally unable to detect anticorrelation between noise sequences. This inability rules out motion opponency as a viable model for human front-end ("early") motion vision.

Adult↗