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Eye movements evoked by proprioceptive stimulation along the body axis in humans.

Proprioceptive input arising from torsional body movements elicits small reflexive eye movements. The functional relevance of these eye movements is still unknown so far. We evaluated their slow components as a function of stimulus frequency and velocity. The horizontal eye movements of seven adult subjects were recorded using an infrared device, while horizontal rotations were applied at three segmental levels of the body [i.e., between head and shoulders (neck stimulus), shoulders and pelvis (trunk stimulus), and pelvis and feet (leg stimulus)]. The following results were obtained: (1) Sinusoidal leg stimulation evoked an eye response with the slow component in the direction of the movement of the feet, while the response to trunk and neck stimulation was oriented in the opposite direction (i.e., in that of the head). (2) In contrast, the gain behavior of all three responses was similar, with very low gain at mid- to high frequencies (tested up to 0.4 Hz) but increasing gain at low frequencies (down to 0.0125 Hz). We show that this gain behavior is mainly due to a gain nonlinearity for low angular velocities. (3) The responses were compatible with linear summation when an interaction series was tested in which the leg stimulus was combined with a vestibular stimulus. (4) There was good correspondence of the median gain curves when eye responses were compared with psychophysical responses (perceived body rotation in space; additionally recorded in the interaction series). However, correlation of gain values on a single-trial basis was poor. (5) During transient neck stimulation (smoothed position ramp), the neck response noticeably consisted of two components -- an initial head-directed eye shift (phasic component) followed by a shift in the opposite direction (compensatory tonic component). Both leg and neck responses can be described by one simple, dynamic model. In the model the proprioceptive input is fed into the gaze network via two pathways which differ in their dynamics and directional sign. The model simulates either leg or neck responses by selecting an appropriate weight for the gain of one of the pathways (phasic component). The interaction results can also be simulated when a vestibular path is added. This model has similarities to one we recently proposed for human self-motion perception and postural control. A major difference, though, is that the proprioceptive input to the gaze-stabilizing network is weak (restricted to low velocities), unlike that used for perception and postural control. We hold that the former undergoes involution during ontogenesis, as subjects depend on the functionally more appropriate vestibulo-ocular reflex. Yet, the weak proprioceptive eye responses that remain may have some functional relevance. Their tonic component tends to stabilize the eyes by slowly shifting them toward the primary head position relative to the body support. This applies solely to the earth-horizontal plane in which the vestibular signal has no static sensitivity.

Adult↗

Shift of the beating field of vestibular nystagmus: an orientation strategy?

We investigated in humans whether the shift of the beating field, which is often observed during vestibular nystagmus, could be related to some strategy of orientation. Eye movements were measured with an infrared system during an experiment on self-motion perception in the dark. Subjects were asked to rotate, by means of a joystick, a mobile robot on which they were seated in order to reproduce a previously imposed passive rotation. We suggest that the shift of the ocular beating field is the manifestation of two different orientation strategies based on allocentric and egocentric reference frames, respectively. It is also proposed that subjects who preferably used the first strategy exhibited large shifts of the beating field, while the others who probably used egocentric memory did not exhibit any shift.

Eye Movements↗

Visual attention revealed by an illusion of motion.

Attention is a mechanism to select sensory information. It is a modulatory process which normally cannot be observed as overt responses. A new psychophysical method using an illusion of motion perception allowed us to visualize the field of the magnitude of attention and its dynamic changes. Based on our experiments using this method we suggest that (1) both passive (bottom-up) and active (top-down) attention exert their effects on the early stages of visual processing, (2) active attention can quickly and briefly be replaced by passive attention induced by an external event, but can be restored in about 400 ms, and (3) attention is directed to an object, not space, and follows the object as it moves.

Animals↗

The influence of adaptation on visual motion detection in chronic sixth nerve palsy after treatment with botulinum toxin.

PURPOSE: To investigate changes in visual motion perception after treatment with botulinum toxin in patients with unilateral chronic lateral rectus muscle palsy. METHODS: Five patients and control subjects were asked to report the perceived drift direction of a sinusoidal grating that was initially stationary and then began to accelerate at 0.09 degrees /sec2 in a horizontal direction. The grating had a field size of 18.5 degrees and was presented monocularly with a contrast just above threshold for visibility for central vision. Both the paretic and non-affected eyes were tested. Psychophysical testing was performed under the following conditions: 1) before treatment and testing, patients occluded their paretic eye for at least three days to avoid diplopia. 2) After treatment with botulinum toxin, alignment was corrected and patients stopped occluding their paretic eye for at least three days before testing. The control subjects occluded their non-dominant eye for three days before testing. RESULTS: In condition 1, no differences in motion detection values between patients and control subjects were found. In condition 2, motion detection thresholds were raised approximately 0.15 degrees /sec as compared to pre-treatment values and compared to the control group. CONCLUSIONS: After treatment, a raised threshold for motion detection is one mechanism used to avoid oscillopsia and visuo-vestibular disorientation during head movements in patients with chronic paralytic squint. This study lends evidence that perceptual-adaptive, compensatory mechanisms develop to reduce oscillopsia and disorientation rather than being caused by abnormal cortical motion processing or defective eye muscle action.

Abducens Nerve Diseases↗

Three stages and two systems of visual processing.

Three stages of visual processing determine how internal noise appears to an external observer: light adaptation, contrast gain control and a postsensory/decision stage. Dark noise occurs prior to adaptation, determines dark-adapted absolute thresholds and mimics stationary external noise. Sensory noise occurs after dark adaptation, determines contrast thresholds for sine gratings and similar stimuli, and mimics external noise that increases with mean luminance. Postsensory noise incorporates perceptual, decision and mnemonic processes. It occurs after contrast-gain control and mimics external noise that increases with stimulus contrast (i.e., multiplicative noise). Dark noise and sensory noise are frequency specific and primarily affect weak signals. Only postsensory noise significantly affects the discriminability of strong signals masked by stimulus noise; postsensory noise has constant power over a wide spatial frequency range in which sensory noise varies enormously. Two parallel perceptual regimes jointly serve human object recognition and motion perception: a first-order linear (Fourier) regime that computes relations directly from stimulus luminance, and a second-order nonlinear (nonFourier) rectifying regime that uses the absolute value (or power) of stimulus contrast. When objects or movements are defined by high spatial frequencies (i.e., texture carrier frequencies whose wavelengths are small compared to the object size), the responses of high-frequency receptors are demodulated by rectification to facilitate discrimination at the higher processing levels. Rectification sacrifices the statistical efficiency (noise resistance) of the first-order regime for efficiency of neural connectivity and computation.

Adaptation, Ocular↗

Spatial frequency selective mechanisms underlying the motion aftereffect.

The motion aftereffect (MAE) was used to study the spatial frequency selectivity of suprathreshold motion perception. Observers were adapted to drifting sine-wave gratings confined to a retinal eccentricity of approx. 4 deg. The magnitude of the subsequent MAE was measured while viewing a stationary sine-wave grating test surface of one of a number of spatial frequencies. The largest MAE was found when the spatial frequency of the test stimulus was the same as that of the adapting stimulus. This phenomenon held for spatial frequencies between 0.5 and 4 c/deg, and was robust with changes in contrast of either adapting or test gratings. However, at an adapting spatial frequency of 0.25 c/deg, the peak MAE was observed at 0.5 c/deg. Control experiments indicated that this peak shift was not the result of the reduced number of cycles in the stimulus, nor the temporal frequency. There was no measurable MAE at spatial frequencies lower than 0.25 c/deg. These results suggest the existence of a "lowest adaptable channel" for the motion aftereffect.

Adaptation, Ocular↗

Psychophysical scaling of circular vection (CV) produced by optokinetic (OKN) motion: individual differences and effects of practice.

Vection (V) refers to the compelling visual illusion of self-motion experienced by stationary individuals when viewing moving visual surrounds. The phenomenon is of theoretical interest because of its relevance for understanding the neural basis of ordinary self-motion perception, and of practical importance because it is the experience that makes simulation, virtual reality displays, and entertainment devices more vicarious. This experiment was performed to address whether an optokinetically induced vection illusion exhibits monotonic and stable psychometric properties and whether individuals differ reliably in these (V) perceptions. Subjects were exposed to varying velocities of the circular vection (CV) display in an optokinetic (OKN) drum 2 meters in diameter in 5 one-hour daily sessions extending over a 1 week period. For grouped data, psychophysical scalings of velocity estimates showed that exponents in a Stevens' type power function were essentially linear (slope = 0.95) and largely stable over sessions. Latencies were slightly longer for the slowest and fastest induction stimuli, and the trend over sessions for average latency was longer as a function of practice implying time course adaptation effects. Test-retest reliabilities for individual slope and intercept measures were moderately strong (r = 0.45) and showed no evidence of superdiagonal form. This implies stability of the individual circularvection (CV) sensitivities. Because the individual CV scores were stable, reliabilities were improved by averaging 4 sessions in order to provide a stronger retest reliability (r = 0.80). Individual latency responses were highly reliable (r = 0.80). Mean CV latency and motion sickness symptoms were greater in males than in females. These individual differences in CV could be predictive of other outcomes, such as susceptibility to disorientation or motion sickness, and for CNS localization of visual-vestibular interactions in the experience of self-motion.

Afterimage↗

Neuronal adaptation to visual motion in area MT of the macaque.

The responsivity of primary sensory cortical neurons is reduced following prolonged adaptation, but such adaptation has been little studied in higher sensory areas. Adaptation to visual motion has strong perceptual effects, so we studied the effect of prolonged stimulation on neuronal responsivity in the macaque's area MT, a cortical area whose importance to visual motion perception is well established. We adapted MT neurons with sinusoidal gratings drifting in the preferred or null direction. Preferred adaptation reduced the responsiveness of MT cells, primarily by changing their contrast gain, and this effect was spatially specific within the receptive field. Null adaptation reduced the ability of null gratings to inhibit the response to a simultaneously presented preferred stimulus. While both preferred and null adaptation alter MT responses, these effects probably do not occur in MT neurons but are likely to reflect adaptation-induced changes in contrast gain earlier in the visual pathway.

Adaptation, Physiological↗

Gaze stability of observers watching Op Art pictures.

It has been the matter of some debate why we can experience vivid dynamic illusions when looking at static pictures composed from simple black and white patterns. The impression of illusory motion is particularly strong when viewing some of the works of 'Op Artists, such as Bridget Riley's painting Fall. Explanations of the illusory motion have ranged from retinal to cortical mechanisms, and an important role has been attributed to eye movements. To assess the possible contribution of eye movements to the illusory-motion percept we studied the strength of the illusion under different viewing conditions, and analysed the gaze stability of observers viewing the Riley painting and control patterns that do not produce the illusion. Whereas the illusion was reduced, but not abolished, when watching the painting through a pinhole, which reduces the effects of accommodation, it was not perceived in flash afterimages, suggesting an important role for eye movements in generating the illusion for this image. Recordings of eye movements revealed an abundance of small involuntary saccades when looking at the Riley pattern, despite the fact that gaze was kept within the dedicated fixation region. The frequency and particular characteristics of these rapid eye movements can vary considerably between different observers, but, although there was a tendency for gaze stability to deteriorate while viewing a Riley painting, there was no significant difference in saccade frequency between the stimulus and control patterns. Theoretical considerations indicate that such small image displacements can generate patterns of motion signals in a motion-detector network, which may serve as a simple and sufficient, but not necessarily exclusive, explanation for the illusion. Why such image displacements lead to perceptual results with a group of Op Art and similar patterns, but remain invisible for other stimuli, is discussed.

Adult↗

Visually induced vertical self-motion sensation is altered in microgravity adaptation.

Vertical vection is a phenomenon of self-motion perception in immobile subjects, which is conventionally perceived in the opposite direction of the upward or downward moving visual stimulus. The Austrian scientific cosmonaut experienced reversed vertical vection from sinusoidal stimulation on third and sixth day of space flight as well as immediately postflight. The occurrence of short periods of reversed vection from constant velocity stimulation six months postflight can be interpreted as a reactivation of an "alternative" visual processing mode. This may indicate that microgravity modulations of the neuronal pathways which process visual information for dynamic orientation are not completely extinguished in the processes involved in readaptation to 1-G.

Adaptation, Physiological↗

Motion analysis by feature tracking.

We have developed a two-stage model of motion perception that identifies moving spatial features and computes their velocity, achieving both high spatial localisation and reliable estimates of velocity. Features are detected in each frame by locating the peaks of the spatial local energy functions, as for stationary images (Morrone MC and Burr DC. Proc R Soc Lond 1988;B235:221-245.). The energy functions are calculated for different scales and orientations, and integrated within a temporal Gaussian window. The velocity of features is determined by the direction of maximal elongation of the energy in space-time, evaluated by calculating the three characteristic curvatures of the energy at each feature point. To circumvent the aperture problem, the energy maps are blurred in space by various amounts, and velocity is computed separately for each spatial blur. The Weber fraction of the local curvatures (curvature contrast) describes the spatio-temporal energy elongation at each feature point, giving a reliability index for each velocity estimate. For each point, the velocity of the spatial blur that yielded the highest curvature contrast was selected, with no further constraints, such as rigidity of motion. Dynamic recruitment of operators of different size allows maximum flexibility of the analysis, allowing it to simulate human visual performance in the detection of noise images, transparent motion, some motion illusions, and second-order motion.

Algorithms↗

Modeling the spatiotemporal cortical activity associated with the line-motion illusion in primary visual cortex.

Our large-scale computational model of the primary visual cortex that incorporates orientation-specific, long-range couplings with slow NMDA conductances operates in a fluctuating dynamic state of intermittent desuppression (IDS), which captures the behavior of coherent spontaneous cortical activity, as revealed by in vivo optical imaging based on voltage-sensitive dyes. Here, we address the functional significance of the IDS cortical operating points by investigating our model cortex response to the Hikosaka line-motion illusion (LMI) stimulus-a cue of a quickly flashed stationary square followed a few milliseconds later by a stationary bar. As revealed by voltage-sensitive dye imaging, there is an intriguing similarity between the cortical spatiotemporal activity in response to (i) the Hikosaka LMI stimulus and (ii) a small moving square. This similarity is believed to be associated with the preattentive illusory motion perception. Our numerical cortex produces similar spatiotemporal patterns in response to the two stimuli above, which are both in very good agreement with experimental results. The essential network mechanisms underpinning the LMI phenomenon in our model are (i) the spatiotemporal structure of the LMI input as sculpted by the lateral geniculate nucleus, (ii) a priming effect of the long-range NMDA-type cortical coupling, and (iii) the NMDA conductance-voltage correlation manifested in the IDS state. This mechanism in our model cortex, in turn, suggests a physiological underpinning for the LMI-associated patterns in the visual cortex of anaesthetized cat.

Animals↗

Visual motion cues in prismatic adaptation: evidence of two separate and additive processes.

The present study was based on the assumption that there are two visual channels which provide separate contributions to visuo-motor recalibration following prismatic displacement of the visual field. The functional properties of the two channels were assumed to conform to predictions from the two motion-analyzing systems models of visual motion perception. The results of the present study confirmed the predictions of the model. Whatever the type of illumination (continuous or stroboscopic) central vision utilizes only cues provided by visual exposure of the arm pointing to a stationary target. Peripheral vision utilizes only cues from visual exposure of the arm freely moving against the homogeneous background but this can be prevented by stroboscopic illumination. In peripheral vision, movement cues provided by exposure of a passively moved arm are not processed. In contrast, the processing of visual cues in central vision is unaffected by whether the movements are active or passive, provided that a stationary target is present. The effects of the two channels may be additive or competitive depending on the conditions. Experimental and theoretical implications are discussed.

Cues↗

First- and second-order processing in transient stereopsis.

Large-field stimuli were used to investigate the interaction of first- and second-order pathways in transient-stereo processing. Stimuli consisted of sinewave modulations in either the mean luminance (first-order stimulus) or the contrast (second-order stimulus) of a dynamic-random-dot field. The main results of the present study are that: (1) Depth could be extracted with both the first-order and second-order stimuli; (2) Depth could be extracted from dichoptically mixed first- and second-order stimuli, however, the same stimuli, when presented as a motion sequence, did not result in a motion percept. Based upon these findings we conclude that the transient-stereo system processes both first- and second-order signals, and that these two signals are pooled prior to the extraction of transient depth. This finding of interaction between first- and second-order stereoscopic processing is different from the independence that has been found with the motion system.

Depth Perception↗

Stimulus contrast and the Reichardt detector.

The direction of a drifting grating can become more easily identified when a stationary, flickering grating, with the same spatial and temporal frequencies, is added to it. This amplification has been accepted as evidence that motion perception depends on the product of visual signals elicited before and after a target changes position, as computed by a Reichardt detector. However, amplification is also consistent with a model in which direction identification depends on the product of detection probabilities before and after the position shift. In this paper, we compare the Reichardt detector with a model of Probability Multiplication. For 2-frame sequences, similar results are predicted by Probability Multiplication and a Reichardt model, in which the performance-limiting noise is early (i.e. it is added prior to signal multiplication). Many new and previously published results are consistent with these predictions. Other results are documented in which the amplification is too large to be consistent with Probability Multiplication. To explain these latter results, Reichardt detectors must have both early and late noises.

Discrimination, Psychological↗

Ocular motor system: anatomy and functional magnetic resonance imaging.

This article reviews current positron emission tomography and functional MR imaging (fMRI) studies of brain activation and indicates some of the insights they provide into the neuronal network mediating motion-perception and ocular motor control. The complexity of the network and the activation of the entire system seemingly independent of the specific ocular motor task performed makes functional interpretation extremely difficult. At the same time, however, the complexity illustrates the dilemma of associating a particular locus with one specific function. Caution is required to differentiate specific from nonspecific effects, to identify activations and deactivations, and to distinguish which of the systems has been activated inadvertently through poor stimulus control. The next step required for meaningful correlations of structure with function is for fMRI studies to test neurologic patients with distinct and separate lesions of the network. Such a comparison must evaluate the effect of the ocular motor deficit on the lesion site and the connected network in the acute stage and then following functional recovery caused by plasticity and neuronal repair.

Brain↗

Intraattribute and interattribute motion induction.

The phenomenon of motion induction occurs, for example, when a bar that is presented next to a spot, which itself was presented slightly earlier, is not correctly perceived to appear everywhere simultaneously, but seems to grow out of the spot. The spot is said to prime one end of the bar. Experiments have been designed to throw more light on the local and global aspects of this phenomenon, in particular to establish whether this illusory motion percept can be observed when the spot and the bar stimuli are defined with respect to the background by one of a variety of attributes, such as luminance, color, stereodepth (crossed and uncrossed), texture, and motion (start and stop). It was found that all attribute combinations supported motion induction readily, but that the strength of the perceived motion (as measured by magnitude estimation) varied and depended more on the attribute defining the bar than on the attribute of the spot. Luminance and color gave the most vivid effects, whereas motion and depth showed the least vivid effects. The influence of the amount of luminance and color contrast on the strength of the effect was also determined and it was found that these variables affected motion induction most at very low contrast levels close to detection threshold. It is concluded that the illusory motion in this effect depends only slightly on the particular visual attribute channel that carries the stimulus information. This is consistent with the contention that it is a high-level, attention-related effect, phenomenologically similar to polarized gamma movement.

Attention↗

Testing the Bayesian model of perceived speed.

In a recent Bayesian model by Weiss, Simoncelli, and Adelson, motion perception is biased by a prior favoring slow speeds. This model predicts qualitatively an impressive variety of phenomena, including the dependence of perceived speed on contrast. We show that the model can also generate quantitative predictions: for a drifting grating with contrast c, perceived speed is proportional to c(q)/(k(q) + c(q)), with k, q constants. We tested this expression on measurements of perceived speed as a function of contrast. Observers indicated the slower of two drifting gratings, a test and a standard. For each test contrast we found the test speed that appeared to match the standard speed. The model fits the data, but only if q is less than 2, the value it would have if the internal representation of contrast were linear. The Bayesian model can make correct quantitative predictions, but needs to be extended to incorporate a more realistic, nonlinear representation of contrast.

Bayes Theorem↗