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Attentional modulation of visual motion perception.

How is the perception and processing of visual motion affected by attention? This review examines recent research in cognition, perception and neurophysiology that explores how ongoing behavioural tasks (and the attentional states they impose) modulate the processing of visual motion. Although traditional views hold that motion is processed in an obligatory, 'pre-attentive' manner, evidence for processing in a task-independent manner is scant. Recent studies of human perception that have measured motion priming, motion aftereffects, uncertainty effects, and motion-interaction effects indicate instead that even simple aspects of motion processing may be substantially affected by whether motion information in a task is used or ignored by the perceiver. Single-unit studies in brain areas sensitive to visual motion in monkeys, and functional imaging studies on humans, also indicate that task and attentional state affect activity levels in brain regions thought to be important in motion perception. This review brings together these converging findings of attentional modulation of motion perception and considers them in light of object-oriented theories of attention.

Journal Article↗

DYNAMICS OF MOTION PERCEPTION IN THE DESERT LOCUST.

The torque produced by the neck muscles of a locust mounted coaxially in an illuminated cylindrical striped drum follows small sinusoidal oscillations of the drum. Peak-to-peak oscillations of 0.03 degree (+/- 0.02 degree) at 0.1 cy/sec elicit measurable responses. Several features of this visual response to drum oscillation can be expected theoretically on the basis of a formal neural mechanism similar to that inferred by Hassenstein and Reichardt for constant-velocity motion perception in the bettle eye.

Animals↗

The spatial and temporal organisation of motion perception units in human vision.

Measurements of threshold illumination levels for detection of retinally non-localised moving targets show that detection of a moving target is influenced by both the spatial and the temporal modulation of the background field. The temporal response characteristics obtained from these measurements are similar to those obtained from experiments on detection of temporal flicker. Experiments with spatially modulated background fields reveal visual mechanisms with spatial properties which are essentially independent of many stimulus parameters. The response amplitude of the spatial filter which characterises these mechanisms increases linearly as a function of background contrast and is independent of the relative orientation between the background structure and the direction of target movement. These properties are used to compute the two-dimensional spatial characteristics of mechanisms involved in the detection of moving targets.

Adult↗

Apparent motion perception: the contribution of the binocular and monocular systems. An improved test based on motion aftereffects.

Research concerning the perception of apparent motion is not easy to conduct: it is hard to obtain quantitative results that can be easily interpreted. A solution to this problem is the use of motion aftereffects (MAEs). Adapting subjects to a specific type of motion leads to apparent motion in the opposite direction when the stimulus is removed. However, subjects are aware of the change in stimulus conditions. A new dynamic test stimulus is proposed in order to avoid artefacts introduced by the awareness of the conditions by the subject. A model, derived from earlier observations, is described which includes contributions from monocular and binocular systems. Results from an experiment in which the dynamic test stimulus was used show that they do not necessarily reproduce the results obtained with a static test stimulus. Central monocular systems are added to the model to account for this discrepancy. The 'pooling hypothesis', which states that the MAE is a weighted mean of the processes involved, permits the estimation of the weights of the individual subsystems. The results of the experiments are explained in terms of this hypothesis by the new model.

Adaptation, Ocular↗

Delay of pattern electroretinogram peaks and its correlation to contrast threshold for motion perception in glaucoma.

Peak latencies of pattern electroretinogram (PERG) were compared between glaucomatous eyes and non-glaucomatous eyes. Contrast threshold for motion perception (CTMP) was also measured with a new device in addition to routine static contrast sensitivity, static visual field and visual acuity. In the present recording, configurations for PERG, i.e. low reversal rate, low mean luminance and presence of background illumination, the PERG peak and trough (P1 and N2, respectively) latencies, were significantly prolonged in the glaucomatous eyes. Although both of the two PERG latencies were strongly correlated with the CTMP, only the P1 peak latency was strongly correlated with the perimetric indices. These results suggest that the P1 and N2 latencies reflect different aspects of signal processing in the retina, especially for moving targets.

Adolescent↗

Functional cerebral asymmetry in auditory motion perception.

Several studies have shown a right-hemispheric advantage for sound localisation. However, most of these studies used stationary sound stimuli, although in most everyday situations humans are in motion when localising sound, or face a moving sound source. To elucidate the question of a functional asymmetry in cortical processing of auditory motion information, we tested 23 neurologically healthy human participants. Virtual leftward or rightward motion (broadband noise) was presented with variable movement angles (MA) in the horizontal plane (via headphones) in either the participants' left or right hemispace. Participants had to indicate whether the sound moved left or rightward. The frequency of "right" judgements determined as a function of MA had a sigmoidal shape in both hemispaces, indicating significant overall discrimination of motion direction. However, the frequency of correct judgements revealed a significantly better performance for the left than for the right hemispace, suggesting a superiority of the right hemisphere. This finding is in agreement with recent neuroimaging results showing higher right-hemispheric activity during localisation of moving sounds. The results might also point to a supramodal right-hemisphere advantage in the attentional processing of motion perception.

Adolescent↗

Functional MRI studies of human visual motion perception: texture, luminance, attention and after-effects.

Motion of an object is thought to be perceived independently of the object's surface properties. However, theoretical, neuropsychological and psychophysical observations have suggested that motion of textures, called 'second-order motion', may be processed by a separate system from luminance-based, or 'first-order', motion. Functional magnetic resonance imaging (fMRI) responses during passive viewing, attentional modulation and post-adaptation motion after-effects (MAE) of these stimuli were measured in seven retinotopic visual areas (labeled V1, V2, V3, VP, V4v, V3A and LO) and the motion-sensitive area MT/MST (V5). In all visual areas, responses were strikingly similar to motion of first- and second-order stimuli. These results differ from a prior investigation, because here the motion-specific responses were isolated. Directing attention towards and away from the motion elicited equivalent response modulation for the two types. Dramatic post-adaptation (MAE) differences in perception of the two stimuli were observed and fMRI activation mimicked perceptual changes, but did not reveal the processing differences. In fact, no visual area was found to respond selectively to the motion of second-order stimuli, suggesting that motion perception arises from a unified motion detection system.

Adolescent↗

Motion perception during involuntary eye vibration.

Retinal motion caused by reflexive or voluntary eye movements is rarely misinterpreted as object motion, as if the visual system discounted the contribution of these eye movements to retinal motion. Yet, involuntary eye movements caused by mechanical eye vibration is often interpreted as object motion unless the vibration has high frequency, in which case only image blur may be noticed. In these latter conditions, however, a light flickering above the fusion limit is vividly perceived to undergo oscillatory motion over its static surround. We determined the conditions of this phenomenon, showing that the perceived frequency of illusory oscillation equals the difference between flicker frequency and the frequency of vibration of the eyes. This outcome is explained as a result of the low-pass temporal frequency characteristic of vision, which further predicts that the same effect should occur if the flickering light is vibrated and observed with static eyes. This prediction was corroborated empirically. We also determined the minimal amplitude of oscillation required to perceive motion as a function of postural stability and the presence of static references, finding an amplitude threshold of approximately 1 arcmin with postural stability in dim-light conditions, which increases to approximately 2 arcmin with postural instability in the dark.

Eye Movements↗

Motion perception and Alzheimer's disease.

The motion sensitivity of 15 probable Alzheimer disease (AD) patients and 15 healthy elderly adults was investigated with a correlated motion paradigm. The AD patients exhibited significantly higher thresholds for detecting the direction of motion. Contrast sensitivity for a 2 cpd, 7.5 Hz counterphased stimulus was related to motion threshold in the AD group. There also was a significant relationship between an index of dementia severity, Mini-Mental State Exam (MMSE), and motion sensitivity. The results support the hypothesis proposed from neuroanatomical evidence by Hof and Morrison (1990) that AD results in a disruption of the visual signals mediated by area 17. Further, the data suggest that this disruption of visual processing is linked to the progression of dementia. The study offers support for the hypothesis that AD leads to a deficit in the magnocellular or M pathway of visual processing.

Aged↗

Insect motion perception.

The first step in this work of reconstruction of a theory of insect vision was to demonstrate that visual behaviour relies on scanning by self-motion and apparently involves measurement of angular velocities of contrasts moving across the eye. The next step was to demonstrate that parallax is also significant as a way of segmenting the visual scene into separate objects. There followed a series of experiments to rule out the existing theory that motion perception depends on autocorrelation, and at the same time an alternative theory was developed. The new theory assumes that at the level of the optic medulla there are numerous parallel channels on each visual axis, representing different neurons, all looking out for their specific combination of signals. The combinations are formed by positive, negative or no-change temporal contrasts at two adjacent visual axes at two successive times, forming 3(4) = 81 possible templates. Simulation of this highly parallel system shows that it can represent the moving image in a compact form that would be adequate to explain what is known for motion and form vision (but not colour vision) in insects. Form, like colour, would be seen as the ratio of numbers of responses of particular templates, in the same way that colours are seen as ratios of responses of receptors for different wavelengths.(ABSTRACT TRUNCATED AT 250 WORDS)

Algorithms↗

A model for direction selectivity in threshold motion perception.

Thresholds were measured for a moving line superimposed on moving sinusoidal gratings. When line and grating moved in the same direction significant subthreshold summation was observed over a range of spatial frequencies. For motion of the line and grating in opposite directions, summation was never observed. This supports the hypothesis that direction selective mechanisms are responsible for motion perception at threshold. Further analysis of the data produced estimates of the spatial frequency tuning of these mechanisms. A quantitative model is proposed to interpret the data, and it is suggested that flickering gratings are not decomposed into their moving components by the visual system.

Cybernetics↗

Comparison of two Simon tasks: neuronal correlates of conflict resolution based on coherent motion perception.

The present study aimed at characterizing the neural correlates of conflict resolution in two variations of the Simon effect. We introduced two different Simon tasks where subjects had to identify shapes on the basis of form-from-motion perception (FFMo) within a randomly moving dot field, while (1) motion direction (motion-based Simon task) or (2) stimulus location (location-based Simon task) had to be ignored. Behavioral data revealed that both types of Simon tasks induced highly significant interference effects. Using event-related fMRI, we could demonstrate that both tasks share a common cluster of activated brain regions during conflict resolution (pre-supplementary motor area (pre-SMA), superior parietal lobule (SPL), and cuneus) but also show task-specific activation patterns (left superior temporal cortex in the motion-based, and the left fusiform gyrus in the location-based Simon task). Although motion-based and location-based Simon tasks are conceptually very similar (Type 3 stimulus-response ensembles according to the taxonomy of [Kornblum, S., Stevens, G. (2002). Sequential effects of dimensional overlap: findings and issues. In: Prinz, W., Hommel., B. (Eds.), Common mechanism in perception and action. Oxford University Press, Oxford, pp. 9-54]) conflict resolution in both tasks results in the activation of different task-specific regions probably related to the different sources of task-irrelevant information. Furthermore, the present data give evidence those task-specific regions are most likely to detect the relationship between task-relevant and task-irrelevant information.

Adult↗

Neural dynamics of motion perception: direction fields, apertures, and resonant grouping.

A neural network model of global motion segmentation by visual cortex is described. Called the motion boundary contour system (BCS), the model clarifies how ambiguous local movements on a complex moving shape are actively reorganized into a coherent global motion signal. Unlike many previous researchers, we analyze how a coherent motion signal is imparted to all regions of a moving figure, not only to regions at which unambiguous motion signals exist. The model hereby suggests a solution to the global aperture problem. The motion BCS describes how preprocessing of motion signals by a motion oriented contrast (MOC) filter is joined to long-range cooperative grouping mechanisms in a motion cooperative-competitive (MOCC) loop to control phenomena such as motion capture. The motion BCS is computed in parallel with the static BCS of Grossberg and Mingolla (1985a, 1985b, 1987). Homologous properties of the motion BCS and the static BCS, specialized to process motion directions and static orientations, respectively, support a unified explanation of many data about static form perception and motion form perception that have heretofore been unexplained or treated separately. Predictions about microscopic computational differences of the parallel cortical streams V1-->MT and V1-->V2-->MT are made--notably, the magnocellular thick stripe and parvocellular interstripe streams. It is shown how the motion BCS can compute motion directions that may be synthesized from multiple orientations with opposite directions of contrast. Interactions of model simple cells, complex cells, hyper-complex cells, and bipole cells are described, with special emphasis given to new functional roles in direction disambiguation for endstopping at multiple processing stages and to the dynamic interplay of spatially short-range and long-range interactions.

Animals↗

Object motion perception is shaped by the motor control mechanism of ocular pursuit.

It is still a matter of debate whether the control of smooth pursuit eye movements involves an internal drive signal from object motion perception. We measured human target velocity and target position perceptions and compared them with the presumed pursuit control mechanism (model simulations). We presented normal subjects (Ns) and vestibular loss patients (Ps) with visual target motion in space. Concurrently, a visual background was presented, which was kept stationary or was moved with or against the target (five combinations). The motion stimuli consisted of smoothed ramp displacements with different dominant frequencies and peak velocities (0.05, 0.2, 0.8 Hz; 0.2-25.6 degrees /s). Subjects always pursued the target with their eyes. In a first experiment they gave verbal magnitude estimates of perceived target velocity in space and of self-motion in space. The target velocity estimates of both Ns and Ps tended to saturate at 0.8 Hz and with peak velocities >3 degrees /s. Below these ranges the velocity estimates showed a pronounced modulation in relation to the relative target-to-background motion ('background effect'; for example, 'background with'-motion decreased and 'against'-motion increased perceived target velocity). Pronounced only in Ps and not in Ns, there was an additional modulation in relation to the relative head-to-background motion, which co-varied with an illusion of self-motion in space (circular vection, CV) in Ps. In a second experiment, subjects performed retrospective reproduction of perceived target start and end positions with the same stimuli. Perceived end position was essentially veridical in both Ns and Ps (apart from a small constant offset). Reproduced start position showed an almost negligible background effect in Ns. In contrast, it showed a pronounced modulation in Ps, which again was related to CV. The results were compared with simulations of a model that we have recently presented for velocity control of eye pursuit. We found that the main features of target velocity perception (in terms of dynamics and modulation by background) closely correspond to those of the internal drive signal for target pursuit, compatible with the notion of a common source of both the perception and the drive signal. In contrast, the eye pursuit movement is almost free of the background effect. As an explanation, we postulate that the target-to-background component in the target pursuit drive signal largely neutralises the background-to-eye retinal slip signal (optokinetic reflex signal) that feeds into the eye premotor mechanism as a competitor of the target retinal slip signal. An extension of the model allowed us to simulate also the findings of the target position perception. It is assumed to be represented in a perceptual channel that is distinct from the velocity perception, building on an efference copy of the essentially accurate eye position. We hold that other visuomotor behaviour, such as target reaching with the hand, builds mainly on this target position percept and therefore is not contaminated by the background effect in the velocity percept. Generally, the coincidence of an erroneous velocity percept and an almost perfect eye pursuit movement during background motion is discussed as an instructive example of an action-perception dissociation. This dissociation cannot be taken to indicate that the two functions are internally represented in separate brain control systems, but rather reflects the intimate coupling between both functions.

Adult↗

Head-centred motion perception in the ageing visual system.

Stationary objects appear to move in the opposite direction to a pursuit eye movement (Filehne illusion) and moving objects appear slower when pursued (Aubert-Fleischl phenomenon). Both illusions imply that extra-retinal, eye-velocity signals lead to lower estimates of speed than corresponding retinal motion signals. Intriguingly, the velocity (i.e. speed and direction) of the Filehne illusion depends on the age of the observer, especially for brief display durations (Wertheim and Bekkering, 1992). This suggests relative signal size changes as the visual system matures. To test the signal-size hypothesis, we compared the Filehne illusion and Aubert-Fleischl phenomenon in young and old observers using short and long display durations. The trends in the Filehne data were similar to those reported by Wertheim and Bekkering. However, we found no evidence for an effect of age or duration in the Aubert-Fleischl phenomenon. The differences between the two illusions could not be reconciled on the basis of actual eye movements made. The findings suggest a more complicated explanation of the combined influence of age and duration on head-centred motion perception than that described by the signal-size hypothesis.

Adult↗

Effects of glaucoma and aging on photopic and scotopic motion perception.

PURPOSE: To examine the effects of primary open-angle glaucoma and normal aging on visual sensitivity for targets known to bias responses from the magnocellular visual processing stream. METHODS: Contrast sensitivity was measured for the detection and direction discrimination of low-spatial-frequency (0.5 cyc/deg), drifting (4-24 Hz) sinusoidal gratings in 15 patients with glaucoma (mean age, 58.7 years), 14 age-matched control subjects (mean age 55.8 years), and 10 young control subjects (mean age, 24.4 years). As a control, sensitivity was measured for the detection of stationary stimuli. Stimuli of 4.7 degrees square were presented at either 0 degrees eccentricity or at 20 degrees along the nasal horizontal meridian, under both photopic and scotopic levels of lighting. RESULTS: Across a wide range of conditions, the ability to detect and discriminate visual motion declined significantly (P < 0.05) with increasing age, whereas the ability to detect stationary patterns was generally unaffected. The rate of decline was adequately described by a simple linear function. Control studies showed that the age-related motion sensitivity losses could not be attributed solely to decreases in retinal illuminance associated with increasing age. Of note, however, there were no significant differences in mean sensitivity between glaucoma and age-matched control groups for any of the conditions used. CONCLUSIONS: Even under conditions believed to bias the response of the visual system to the magnocellular pathway, glaucoma subjects could not be reliably differentiated from control subjects on the basis of mean sensitivity to motion stimuli. The findings have two broad implications: first, that substantial neural loss specific for motion perception occurs during the processes of normal aging, and second, that sensitivity to motion targets per se may not be a useful indicator of neural integrity in the early stages of glaucoma.

Adult↗