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PubMed1996

Interactions between self-motion and depth perception in the processing of optic flow.

Moving and acting in a 3D environment requires the perception of its 3D structure. Vision is known to play a crucial role in the control of self-motion, particularly through the changes in the retinal image subsequent to movements of the observer. Reciprocally, signals related to self-motion can also influence our visual perception of 3D space. These interactions between 3D visual perception and self-motion, as demonstrated behaviourally, are now better understood thanks to the development of computational models for processing moving images. They also bear a particular interest in the context of the recent intensive exploration of the inferior parietal lobe (IPL) by neurophysiologists. The IPL is now firmly established as one site of interaction between 3D visual perception and motor control. The parallel between behaviour and neurophysiology leads to a set of crucial, yet unanswered, questions.

Humans↗
PubMed1998

Anisotropies in visual motion perception: a fresh look.

We measured motion-detection and motion-discrimination performance for different directions of motion, using stochastic motion sequences. Random-dot cinematograms containing 200 dots in a circular aperture were used as stimuli in a two-interval forced-choice procedure. In the motion-detection experiment, observers judged which of two intervals contained weak coherent motion, the other internal containing random motion only. In the direction-discrimination experiment, observers viewed a standard direction of motion followed by comparison motion in a slightly different direction. Observers indicated whether the comparison was clockwise or counterclockwise, relative to the standard. Twelve directions of motion were tested in the detection task and five standard directions (three cardinal directions and two oblique directions) in the discrimination task. Detection thresholds were invariant with direction of motion, but direction-discrimination thresholds were significantly higher for motion in oblique directions, even at low-coherence levels. Results from control conditions ruled out monitor artifacts and indicate that the oblique effect is relative to retinal coordinates. These results have broad implications for computational and physiological models of motion perception.

Anisotropy↗
PubMed2006

Visual recalibration and selective adaptation in auditory-visual speech perception: Contrasting build-up courses.

Exposure to incongruent auditory and visual speech produces both visual recalibration and selective adaptation of auditory speech identification. In an earlier study, exposure to an ambiguous auditory utterance (intermediate between /aba/ and /ada/) dubbed onto the video of a face articulating either /aba/ or /ada/, recalibrated the perceived identity of auditory targets in the direction of the visual component, while exposure to congruent non-ambiguous /aba/ or /ada/ pairs created selective adaptation, i.e. a shift of perceived identity in the opposite direction [Bertelson, P., Vroomen, J., & de Gelder, B. (2003). Visual recalibration of auditory speech identification: a McGurk aftereffect. Psychological Science, 14, 592-597]. Here, we examined the build-up course of the after-effects produced by the same two types of bimodal adapters, over a 1-256 range of presentations. The (negative) after-effects of non-ambiguous congruent adapters increased monotonically across that range, while those of ambiguous incongruent adapters followed a curvilinear course, going up and then down with increasing exposure. This pattern is discussed in terms of an asynchronous interaction between recalibration and selective adaptation processes.

Adaptation, Physiological↗
PubMed1995

The consequences of inactivating areas V1 and V5 on visual motion perception.

We studied the capacity of normal humans to discriminate the direction of motion of visual stimuli when areas V1 or V5 were reversibly inactivated with transcranial magnetic stimulation. We found that (i) magnetic stimulation of V5 at intervals of -20 to +10 ms before or after the onset of visual stimulation was effective in abolishing motion perception--other delays were not; (ii) magnetic stimulation of V1 abolished motion perception only marginally and at delays which were significantly different from those obtained with V5, the stimulation now being effective only at delays of 60-70 ms after the onset of visual stimulation. We conclude (i) that stimulation of V5 is a much more potent way of inducing akinetopsia (motion imperception) than stimulation of V1; (ii) that perceptually effective visual motion signals reach V5 at or before 30 ms and reach V1 at or before 60 ms--consequently, perceptually effective motion signals reach V5 before they reach V1; (iii) that, given the time course of arrival of signals in V1 and V5, it takes about 30-50 ms for signals from V1 to reach V5. We conclude further that there are probably two components reaching V5 from the retina, a fast one which bypasses V1 and a slow one which reaches it through V1.

Brain Mapping↗
PubMed2004

The influence of phonological neighborhood on visual word perception.

In the research reported here, we investigated the influence of phonological neighborhood density on the processing of words in the visual lexical decision task. The results of the first experiment revealed that words with large phonological neighborhoods were verified more rapidly than words with small phonological neighborhoods. In the second experiment, we replicated this effect with a more tightly controlled set of stimuli. These results demonstrate the importance of phonological codes when processing visually presented letter strings. We relate this research to previous results on semantic and orthographic neighborhoods and discuss the results within the context of a model in which lexical decisions are based on stimulus familiarity.

Decision Making↗
PubMed1977

Cluster analyses of measures of sensory integration.

Cluster analyses of intercorrelation of scores on tests of sensory integrative, language, auditory, intellectual, and academic tests administered to young learning-disabled school children demonstrated a close relationship between academic achievement, the right ear score on dichotic listening, language expression, and auditory memory. Visual perception tests and the Auditory Association sub-test of the Illinois Test of Psycholinguistic Abilities showed a close association with IQ. Others associations were consistent with the view that when the two cerebral hemispheres do not corroborate, both hemispheres tend to develop similar motor and language functions. Analyses of the intercorrelation of scores on the sensory integration, auditory, and language tests resulted in four major factors: auditory-language functions, postural-ocular reactions, eye-hand coordination, and somatosensory and motor planning or praxis. A fifth factor, visual perception, contributed less to the final factor structure.

Achievement↗
PubMed1991

Selective directional sensitivity in visual motion perception.

We present two experiments demonstrating that: (i) the latency of perception of the position of a small visual target moving towards the fovea is shorter than that of the same target moving away from the fovea; (ii) the reaction time (RT) to onset of motion of the same type of target is also shorter when it moves towards the fovea; and (iii) the RT to onset of motion away from the fovea may be shorter when larger, textured stimuli are employed. The relation of the findings to the existence of two systems for visual motion information processing and to recent neurophysiological findings is discussed.

Adult↗
PubMed1997

The TINS Lecture. The parietal association cortex in depth perception and visual control of hand action.

Recent neurophysiological studies in alert monkeys have revealed that the parietal association cortex plays a crucial role in depth perception and visually guided hand movement. The following five classes of parietal neurons covering various aspects of these functions have been identified: (1) depth-selective visual-fixation (VF) neurons of the inferior parietal lobule (IPL), representing egocentric distance; (2) depth-movement sensitive (DMS) neurons of V5A and the ventral intraparietal (VIP) area representing direction of linear movement in 3-D space; (3) depth-rotation-sensitive (RS) neurons of V5A and the posterior parietal (PP) area representing direction of rotary movement in space; (4) visually responsive manipulation-related neurons (visual-dominant or visual-and-motor type) of the anterior intraparietal (AIP) area, representing 3-D shape or orientation (or both) of objects for manipulation; and (5) axis-orientation-selective (AOS) and surface-orientation-selective (SOS) neurons in the caudal intraparietal sulcus (cIPS) sensitive to binocular disparity and representing the 3-D orientation of the longitudinal axes and flat surfaces, respectively. Some AOS and SOS neurons are selective in both orientation and shape. Thus the dorsal visual pathway is divided into at least two subsystems, V5A, PP and VIP areas for motion vision and V6, LIP and cIPS areas for coding position and 3-D features. The cIPS sends the signals of 3-D features of objects to the AIP area, which is reciprocally connected to the ventral premotor (F5) area and plays an essential role in matching hand orientation and shaping with 3-D objects for manipulation.

Animals↗
PubMed1982

[Partial acoustic agnosia as a cause of stammering. Possibilities and limits of diagnostic testing methods].

An essential precondition for normal speech development is an intact peripheral and central hearing capacity. Disturbances of auditory perception can be the cause of speech defects. There are many methods to examine sound discriminating capacity. Most of them are statistically not verified or standardized. We developed a testing method which consists of 44 figured word pairs. We suggest how to differentiate between children with impaired auditory perception from children without this disturbance. Visual perception and visuomotor function were examined by the Marianne Frostig Developmental Test of VIsual Perception and the Bender-Gestalt-Test (Göttinger Form-reproduktions-Test). We found disturbances all the more the auditory perception was impaired. We investigated handedness and cerebral dominance by the Hand-Dominanz-Test (Steingrüber, Lienert). Righthandedness was most clearly pronounced in the control group (normal speaking children), less so in stammerers without weakness in sound discrimination and weakest in stammerers with this latter defect.

Agnosia↗
PubMed2002

Integration of multiple motion vectors over space: an fMRI study of transparent motion perception.

Visual scenes are frequently composed of objects that move in different directions. To segment such scenes into distinct objects or image planes, local motion cues have to be evaluated and integrated according to criteria of global coherence. When several populations of coherently moving random dots penetrate each other, the visual system tends to assign them to different planes-perceived as transparent motion. This process of integration was studied by changing the angle of motion trajectories with which groups of dots penetrate each other or by varying the spatial constellation of dots moving in opponent directions. Psychophysical testing revealed that stimuli providing almost identical local motion cues could be perceived in three very different ways: (1) as a matrix of stationary flickering dots, (2) as a single surface of coherently moving dots, and (3) as two transparent dot matrices moving in different directions. Behaviorally controlled functional magnetic resonance imaging (fMRI) was used to identify brain regions that contribute to the integration of local motion cues into coherently moving surfaces. Activation of the human motion complex (hMT+/V5) and of areas in the fusiform gyrus (FG) as well as in the intraparietal sulcus (IPS-occ) was correlated with the perception of coherent motion and especially hMT+/V5 took a central role in differentiating transparent motion from single-surface coherent motion.

Adult↗
PubMed1999

Cognitive processing of drawing abilities.

This critical review examines constructional apraxia from a cognitive neuropsychological perspective. To our knowledge, van Sommers (1989) is the only researcher to present a global cognitive model of drawing abilities. He organizes it into two hierarchical systems: Marr's model of visual perception and a graphic production system. The latter comprises four hierarchically organized components: depiction decisions, production strategy, contingent planning, and articulatory and economic constraints. Van Sommers' model will be discussed in light of other models and on the basis of empirical neuropsychological studies (Farah, 1984; Kosslyn & Koenig, 1992; Roncato, Sartori, Masterson, & Rumiati, 1987; van Sommers, 1989). We find that: (1) the Kosslyn and Koenig visual perception model describes more accurately the perceptual components underlying copying than the visual perception system of van Sommers' drawing model, (2) Van Sommers' arguments in favor of a depiction processing as opposed to visual imagery are not convincing, (3) Van Sommers' assumption that a production strategy is a component is unclear, and (4) articulatory and economic constraints are not cognitive components, but constraints imposed during action programming. This literature review leads to a discussion of future research topics and the specificity of constructional apraxia.

Apraxias↗
PubMedDate not supplied

Using afterimages to test neural mechanisms for perceptual filling-in.

Many theories of visual perception propose that brightness information spreads from edges to define the perceived intensity of the interior of visual surfaces. Several theories of visual perception have hypothesized that this filling-in process is similar to a diffusion of information where the signals coding brightness spread to nearest neighbors. This paper shows that diffusive mechanisms fail to account for the characteristics of certain afterimage percepts that seem to be dependent on the filling-in process. A psychophysical experiment tests a key property of diffusion-based filling-in mechanisms and finds data that rejects this class of models. A non-diffusive based filling-in mechanism is proposed and is shown to act much like the diffusive based mechanism in many instances, but also produces afterimage percepts that match the experimental data.

Afterimage↗