Guillaume S. Masson

Postural effects of motion vision in young autistic children

&NA; We present the first assessment of motion vision in childhood autism. Postural reactivity to visually perceived motion was measured in five autistic children and 12 normal controls of the same chronological age. Anteroposterior as well as total body sway occurring on a force platform in response to movements in the visual environment were compared. Autistic children were posturally more unstable than normal children and quite insensitive to visually perceived environmental motion. Some implications of this impairment for sensorimotor and social communication development in infantile autism are discussed.

Dopaminergic modulation of visual sensitivity in man

Summary— A large body of experimental evidence supports the hypothesis that dopamine is a functional neuromodulator at many levels of the visual system. Intrinsic dopaminergic neurons were characterized in most mammalian retina, including man. These neurons give rise to a dendritic plexus covering the retina. Thus, dopamine seems to be involved in the organization of the ganglion cell and the bipolar cell receptive fields and modulates physiological activity of photoreceptors, both processes which underlie sensitivity and spatial selectivity of visual processing in the early stage of the visual system. Moreover, few data are now available concerning the functional significance of dopaminergic modulation of visual sensitivity in man. Parkinsons disease is a specific disorder of central dopaminergic systems. Abnormalities in the pattern‐evoked potentials and electroretinogram have been found in parkinsonian patients. Contrast sensitivity, a useful tool for measuring visual spatio‐temporal sensitivity in man, has also been shown to be modified due to this affection. Dynamic contrast sensitivity is primarily decreased in these patients, distinguishing them from the normal aging process. Because these modifications in shape of the contrast sensitivity function are reversed by L‐Dopa, and that neuroleptic administration could reproduce them in schizophrenian patients, it was suggested that dopamine might tune the contrast sensitivity function in man. We have recently shown that subcutaneous apomorphine induces changes in contrast sensitivity in healthy volunteers, which preferentially affect motion sensitivity. These dopaminergic sensitive modifications in the shape of the contrast sensitivity function might reflect a change in the range of sensitivity of the visual system, both in dynamic and spatial properties. This could be explained by a modification in the spatial and dynamic properties of the ganglion cell responses in the retina. Moreover, we suggest both from our results and from the review of the literature that human psychophysical data confirm the hypothesis that dopamine may be involved in light retinal adaptation, as light‐induced and dopamine‐induced modifications in the shape in the contrast sensitivity function are quite similar.

Motion perception during saccadic eye movements.

During rapid eye movements, motion of the stationary world is generally not perceived despite displacement of the whole image on the retina. Here we report that during saccades, human observers sensed visual motion of patterns with low spatial frequency. The effect was greatest when the stimulus was spatiotemporally optimal for motion detection by the magnocellular pathway. Adaptation experiments demonstrated dependence of this intrasaccadic motion percept on activation of direction-selective mechanisms. Even two-dimensional complex motion percepts requiring spatial integration of early motion signals were observed during saccades. These results indicate that the magnocellular pathway functions during saccades, and that only spatiotemporal limitations of visual motion perception are important in suppressing awareness of intrasaccadic motion signals.

Effects of stationary and moving textured backgrounds on the visuo-oculo-manual tracking in humans

We investigated the effects of stationary and moving textured backgrounds on ocular and manual pursuit of a discrete target that suddenly starts to move at constant speed (ramp motion). When a stationary textured background was superimposed to the target displacement, the gain of the steady-state eye smooth pursuit velocity was significantly reduced, while the latency of pursuit initiation did not vary significantly, as compared to a dark background condition. The initial velocity of the eye smooth pursuit was also lowered. Both the initial acceleration and the steady-state manual tracking angular velocity were slightly, but not significantly, lowered when compared to a dark background condition. Detrimental effects of the stationary textured background were of comparable amplitude (approximately 10%) for ocular and manual pursuit. In a second condition, we compared ocular and manual pursuit when the textured background was either stationary or drifting. Initial and steady-state eye velocities increased when the textured background moved in the same direction as the target. Conversely, when the background moved in the opposite direction, both velocities were decreased. Eye displacement gain remained however close to unity due to an increase in the occurrence of catch-up corrective saccades. The effects of the moving backgrounds on the initial and steady-state forearm velocities were inverse to that reported for smooth pursuit eye movements. Neither manual nor ocular smooth pursuit latencies were affected.

Dynamics of attentional deployment during saccadic programming.

The dynamics of attentional deployment before saccade execution was studied with a dual-task paradigm. Observers made a horizontal saccade whose direction was indicated by a symbolic precue and had to discriminate the orientation of a Gabor patch displayed at different delays after the precue (but before saccade onset). The patch location relative to the saccadic target was indicated to observers before each block. Therefore, on each trial, observers were informed simultaneously about the respective absolute locations of the saccadic and perceptual targets. The main result is that orientational acuity improved over a period of 150-200 ms after the precue onset at the saccadic target location, where overall performance is best, and at distant locations. This effect is due to attentional factors rather than to an alerting effect. It is also dependent on the efficiency of the temporal masks displayed before and after the Gabor patches.

Functional consequences of correlated excitatory and inhibitory conductances in cortical networks

Neurons in the neocortex receive a large number of excitatory and inhibitory synaptic inputs. Excitation and inhibition dynamically balance each other, with inhibition lagging excitation by only few milliseconds. To characterize the functional consequences of such correlated excitation and inhibition, we studied models in which this correlation structure is induced by feedforward inhibition (FFI). Simple circuits show that an effective FFI changes the integrative behavior of neurons such that only synchronous inputs can elicit spikes, causing the responses to be sparse and precise. Further, effective FFI increases the selectivity for propagation of synchrony through a feedforward network, thereby increasing the stability to background activity. Last, we show that recurrent random networks with effective inhibition are more likely to exhibit dynamical network activity states as have been observed in vivo. Thus, when a feedforward signal path is embedded in such recurrent network, the stabilizing effect of effective inhibition creates an suitable substrate for signal propagation. In conclusion, correlated excitation and inhibition support the notion that synchronous spiking may be important for cortical processing.

Visual Perception Modifies Goal-directed Movement Control: Supporting Evidence from a Visual Perturbation Paradigm:

It is well known that dynamic visual information influences movement control, whereas the role played by background visual information is still largely unknown. Evidence coming mainly from eye movement and manual tracking studies indicates that background visual information modifies motion perception and might influence movement control. The goal of the present study was to test this hypothesis. Subjects had to apply pressure on a strain gauge to displace in a single action a cursor shown on a video display and to immobilize it on a target shown on the same display. In some instances, the visual background against which the cursor moved was unexpectedly perturbed in a direction opposite to (Experiment 1), or in the same direction as (Experiment 2) the cursor controlled by the subject. The results of both experiments indicated that the introduction of a visual perturbation significantly affected aiming accuracy. These results suggest that background visual information is used to evaluate the velocity of the aiming cursor, and that this perceived velocity is fed back to the control system, which uses it for on-line corrections.

Short-latency ocular following in humans: sensitivity to binocular disparity

We show that the initial ocular following responses elicited by motion of a large pattern are modestly attenuated when that pattern is shifted out of the plane of fixation by altering its binocular disparity. If the motion is applied to only restricted regions of the pattern, however, then altering the disparity of those regions severely attenuates their ability to generate ocular following. This sensitivity of the ocular tracking mechanism to local binocular disparity would help the observer who moves through a cluttered 3-D world to stabilize objects in the plane of fixation and ignore all others.

Motion perception of saccade-induced retinal translation

Active visual perception relies on the ability to interpret correctly retinal motion signals induced either by moving objects viewed with static eyes or by stationary objects viewed with moving eyes. A motionless environment is not normally perceived as moving during saccadic eye movements. It is commonly believed that this phenomenon involves central oculomotor signals that inhibit intrasaccadic visual motion processing. The keystone of this extraretinal theory relies on experimental reports showing that physically stationary scenes displayed only during saccades, thus producing high retinal velocities, are never perceived as moving but appear as static blurred images. We, however, provide evidence that stimuli optimized for high-speed motion detection elicit clear motion perception against saccade direction, thus making the search for extraretinal suppression superfluous. The data indicate that visual motion is the main cue used by observers to perform the task independently of other perceptual factors covarying with intrasaccadic stimulation. By using stimuli of different durations, we show that the probability of perceiving the stimulus as static, rather than moving, increases when the intrasaccadic stimulation is preceded or followed by a significant extrasaccadic stimulation. We suggest that intrasaccadic motion perception is accomplished by motion-selective magnocellular neurons through temporal integration of rapidly increasing retinal velocities. The functional mechanism that usually prevents this intrasaccadic activity from being perceived seems to rely on temporal masking effects induced by the static retinal images present before and/or after the saccade.

Ocular responses to motion parallax stimuli : The role of perceptual and attentional factors

When human subjects are presented with visual displays consisting of random dots moving sideways at different velocities, they perceive transparent surfaces, moving in the same direction but located at different distances from themselves. They perceive depth from motion parallax, without any additional cues to depth, such as relative size, occlusion or binocular disparity. Simultaneously, large-field visual motion triggers compensatory eye movements which tend to offset such motion, in order to stabilize the visual image of the environment. In a series of experiments, we investigated how such reflexive eye movements are controlled by motion parallax displays, that is, in a situation where a complete stabilization of the visual image is never possible. Results show that optokinetic nystagmus, and not merely active visual pursuit of singular elements, is triggered by such displays. Prior to the detection of depth from motion parallax, eye tracking velocity is equal to the average velocity of the visual image. After detection, eye tracking velocity spontaneously matches the slowest velocity in the visual field, but can be controlled by attentional factors. Finally, for a visual stimulation containing more than three velocities, subjects are no longer able to perceptually dissociate between different surfaces in depth, and eye tracking velocity remains equal to the average velocity of the visual image. These data suggest that, in the presence of flow fields containing motion parallax, optokinetic eye movements are modulated by perceptual and attentional factors.