Motion perception over long interstimulus intervais

Recent studies using moving arrays of textured micropatterns have suggested that motion percep-tion can be supported by two mechanisms, one quasilinear and sensitive to the motion of luminance-defined local texture, the other nonlinear and coding motion of contrast-defined envelopes of texture (Baker & Hess, 1998; Boulton & Baker, 1993b). Here we used similar patterns to study motion percep-tion under conditions previously shown to isolate the nonlinear mechanism (low micropattern densi-ties and positive interstimulus intervals [ISIs]). We measured direction discrimination for two-flash ap-parent motion over a much larger range of ISIs, and susceptibility to masking by incoherently moving “distractor” micropatterns. The results suggest that two nonlinear mechanisms can support motion perception under these conditions. One operates only for relatively short ISIs (less than c. 100 msec), is sensitive to small spatial displacements, and is relatively insensitive to distractor masking. The other operates over much longer ISIs, is insensitive to small spatial displacements, and is highly disrupted by distractor masking. These results are in line with previous studies suggesting that three mechanisms support motion perception.     

Sensitivity to relative and absolute motion.

The threshold of sensitivity to movement could be governed by mechanisms that are sensitive either to change in spatial position, or directly to the movement itself. The use of spatially complex patterns (random-dot patterns) has been suggested to eliminate the former strategy allowing examination of the movement detecting mechanisms in isolation. By means of such a technique, thresholds for directional judgements were determined for patterns which underwent either a simple displacement or a shearing displacement. Thresholds for shearing motion were found to be around one half of those for simple motion, suggesting that relative, rather than absolute, motion governs performance for small displacements. This contrasts with previous experiments which showed that absolute motion governs performance for much larger displacements.     

Cortical dynamics of visual motion perception: short-range and long-range apparent motion.

This article describes further evidence for a new neural network theory of biological motion perception. The theory clarifies why parallel streams V1----V2, V1----MT, and V1----V2----MT exist for static form and motion form processing among the areas V1, V2, and MT of visual cortex. The theory suggests that the static form system (Static BCS) generates emergent boundary segmentations whose outputs are insensitive to direction-of-contrast and to direction-of-motion, whereas the motion form system (Motion BCS) generates emergent boundary segmentations whose outputs are insensitive to direction-of-contrast but sensitive to direction-of-motion. The theory is used to explain classical and recent data about short-range and long-range apparent motion percepts that have not yet been explained by alternative models. These data include beta motion, split motion, gamma motion and reverse-contrast gamma motion, delta motion, and visual inertia. Also included are the transition from group motion to element motion in response to a Ternus display as the interstimulus interval (ISI) decreases; group motion in response to a reverse-contrast Ternus display even at short ISIs; speed-up of motion velocity as interflash distance increases or flash duration decreases; dependence of the transition from element motion to group motion on stimulus duration and size, various classical dependencies between flash duration, spatial separation, ISI, and motion threshold known as Korte's laws; dependence of motion strength on stimulus orientation and spatial frequency; short-range and long-range form-color interactions; and binocular interactions of flashes to different eyes.     

Redundancy effects of a moving distractor generated by alerting and orienting

Redundancy effects refer to improvement of performance in response to irrelevant stimulation, or distractors. Previously described redundancy effects have mainly been associated with relatively high-level perception. The present study examines whether redundancy effects exist in basic attentional and perceptual systems, such as alerting and orienting. Participants performed speeded detection of briefly presented targets while ignoring moving distractors. The presence/absence of distractors and their spatial relationships with targets were manipulated to dissociate possible alerting and orienting redundancies. The distractor pathway (straightforward vs. chaotic) and its motion predictability (blocked vs. intermixed sequences of straightforward and chaotic trials) were also manipulated. The presence of a distractor resulted in faster responses (alerting redundancy). Furthermore, participants responded faster to targets behind distractors (orienting redundancy). Orienting redundancy was found only in the straightforward condition. This indicates that generating an orienting redundancy effect is a relatively slow process based on continuous observation of motion. Lastly, a blocked sequence of trials improved the alerting redundancy effect in comparison with an intermixed sequence.     

Temporal properties in masking biological motion

The perception of biological motion using point light animation techniques was investigated in several experiments. Animations simulating walking were presented with additional masking dots. The temporal properties of the walking motion or the temporal relationship between the walking and masking motions were systematically manipulated. Results showed that (1) perception of biological motion was sensitive to even small temporal perturbation within the walker, (2) the effectiveness of a mask depended upon the temporal phase difference between the mask and point light walker, (3) relatively small temporal differences between the mask and point light walker decreased the effectiveness of the mask, and (4) these effects were not due simply to observers detecting the phase offsets in the display. Temporal properties of the motion are important in perceiving the human form in action, just as in other types of figure-ground segregation. This information may be processed by both motion and form pathways for processing biological motion.     

Object and observer motion in the perception of objects by infants

Sixteen-week-old human infants distinguish optical displacements given by their own motion from displacements given by moving objects, and they use only the latter to perceive the unity of partly occluded objects. Optical changes produced by moving the observer around a stationary object produced attentional levels characteristic of stationary observers viewing stationary displays and much lower than those shown by stationary observers viewing moving displays. Real displacements of an object with no subject-relative displacement, produced by moving an object so as to maintain a constant relation to the moving observer, evoked attentional levels that were higher than with stationary displays and more characteristic of attention to moving displays, a finding suggesting detection of the real motion. Previously reported abilities of infants to perceive the unity of partly occluded objects from motion information were found to depend on real object motion rather than on optical displacements in general. The results suggest that object perception depends on registration of the motions of surfaces in the three-dimensional layout.     

A comparison of auditory and visual apparent motion presented individually and with crossmodal moving distractors

Unimodal auditory and visual apparent motion (AM) and bimodal audiovisual AM were investigated to determine the effects of crossmodal integration on motion perception and direction-of-motion discrimination in each modality. To determine the optimal stimulus onset asynchrony (SOA) ranges for motion perception and direction discrimination, we initially measured unimodal visual and auditory AMs using one of four durations (50, 100, 200, or 400 ms) and ten SOAs (40-450 ms). In the bimodal conditions, auditory and visual AM were measured in the presence of temporally synchronous, spatially displaced distractors that were either congruent (moving in the same direction) or conflicting (moving in the opposite direction) with respect to target motion. Participants reported whether continuous motion was perceived and its direction. With unimodal auditory and visual AM, motion perception was affected differently by stimulus duration and SOA in the two modalities, while the opposite was observed for direction of motion. In the bimodal audiovisual AM condition, discriminating the direction of motion was affected only in the case of an auditory target. The perceived direction of auditory but not visual AM was reduced to chance levels when the crossmodal distractor direction was conflicting. Conversely, motion perception was unaffected by the distractor direction and, in some cases, the mere presence of a distractor facilitated movement perception.     

Detection of stimulus motion in 5-month-old infants

Five-month-old infants were tested by the method of preferential looking for discrimination between a pattern undergoing oscillating apparent motion and an identical static pattern. Sensitivity to small spatial displacements was evident at temporal frequencies of 8 and 16 Hz. Preference for the moving display was related independently to the temporal frequency of oscillation and the magnitude of the spatial displacement. Preferences for the moving display increased asymptotically across spatial displacements from 11 to 89 arc min. Preferences peaked between temporal oscillation frequencies of 8 and 16 Hz. Preference was not related to the ratio of these two variables--velocity. The minimum displacement threshold of 7.36 arc min was found to depend on the size of the elements in the pattern and on the temporal frequency of oscillation. The results demonstrate that motion-sensitive mechanisms responsive to small spatial displacements are present at 5 months of age.     

Effects of the orientation of moving objects on the perception of streaming/bouncing motion displays

In this study, we examined the contribution of the orientation of moving objects to perception of a streaming/bouncing motion display. In three experiments, participants reported which of the two types of motion, streaming or bouncing, they perceived. The following independent variables were used: orientation differences between Gabor micropatterns (Gabors) and their path of motion (all the experiments) and the presence/absence of a transient tone (Experiment 1), transient visual flash (Experiment 2), or concurrent secondary task (Experiment 3) at the coincidence of Gabors. The results showed that the events at coincidence generally biased responses toward the perception of bouncing. On the other hand, alignment of Gabors with their motion axes significantly reduced the frequency of bounce perception. The results also indicated that an object whose orientation was parallel to its motion path strengthened the spatiotemporal integration of local motion signals along a straight motion path, resulting in the perception of streaming. We suggest that the effect of collinearity between Gabors and their motion path is relatively free from the effect of attention distraction.     

Distractor interference during smooth pursuit eye movements

When 2 targets for pursuit eye movements move in different directions, the eye velocity follows the vector average (S. G. Lisberger & V. P. Ferrera, 1997). The present study investigates the mechanisms of target selection when observers are instructed to follow a predefined horizontal target and to ignore a moving distractor stimulus. Results show that at 140 ms after distractor onset, horizontal eye velocity is decreased by about 25%. Vertical eye velocity increases or decreases by 1 degrees /s in the direction opposite from the distractor. This deviation varies in size with distractor direction, velocity, and contrast. The effect was present during the initiation and steady-state tracking phase of pursuit but only when the observer had prior information about target motion. Neither vector averaging nor winner-take-all models could predict the response to a moving to-be-ignored distractor during steady-state tracking of a predefined target. The contributions of perceptual mislocalization and spatial attention to the vertical deviation in pursuit are discussed.     

The effect of experience and of dots’ density and duration on the detection of coherent motion in dogs

Knowledge about the mechanisms underlying canine vision is far from being exhaustive, especially that concerning post-retinal elaboration. One aspect that has received little attention is motion perception, and in spite of the common belief that dogs are extremely apt at detecting moving stimuli, there is no scientific support for such an assumption. In fact, we recently showed that dogs have higher thresholds than humans for coherent motion detection (Kanizsar et al. in Sci Rep UK 7:11259, 2017). This term refers to the ability of the visual system to perceive several units moving in the same direction, as one coherently moving global unit. Coherent motion perception is commonly investigated using random dot displays, containing variable proportions of coherently moving dots. Here, we investigated the relative contribution of local and global integration mechanisms for coherent motion perception, and changes in detection thresholds as a result of repeated exposure to the experimental stimuli. Dogs who had been involved in the previous study were given a conditioned discrimination task, in which we systematically manipulated dot density and duration and, eventually, re-assessed our subjects’ threshold after extensive exposure to the stimuli. Decreasing dot duration impacted on dogs’ accuracy in detecting coherent motion only at very low duration values, revealing the efficacy of local integration mechanisms. Density impacted on dogs’ accuracy in a linear fashion, indicating less efficient global integration. There was limited evidence of improvement in the re-assessment but, with an average threshold at re-assessment of 29%, dogs’ ability to detect coherent motion remains much poorer than that of humans.     

Evidence for the duplex theory of tactile texture perception

Three experiments are reported bearing on Katz's hypothesis that tactile texture perception is mediated by vibrational cues in the case of fine textures and by spatial cues in the case of coarse textures. Psychophysical responses when abrasive surfaces moved across the skin were compared with those obtained during static touch, which does not provide vibrational cues. Experiment 1 used two-interval forced-choice procedures to measure discrimination of surfaces. Fine surfaces that were readily discriminated when moved across the skin became indistinguishable in the absence of movement; coarse surfaces, however, were equally discriminable in moving and stationary conditions. This was shown not to result from any inherently greater difficulty of fine-texture discrimination. Experiments 2 and 3 used free magnitude estimation to obtain a more comprehensive picture of the effect of movement on texture (roughness) perception. Without movement, perception was seriously degraded (the psychophysical magnitude function was flattened) for textures with element sizes below 100 microns; above this point, however, the elimination of movement produced an overall decrease in roughness, but not in the slope of the magnitude function. Thus, two components of stimulation (presumably vibrational and spatial) contribute to texture perception, as Katz maintained; mechanisms for responding to the latter appear to be engaged at texture element sizes down to 100 microns, a surprisingly small value.     

Influences of the perception of self-motion on postural parameters.

We examined how spatial and temporal characteristics of the perception of self-motion, generated by constant velocity visual motion, was reflected in orientation of the head and whole body of young adults standing in a CAVE, a virtual environment that presents wide field of view stereo images with context and texture. Center of pressure responses from a force plate and perception of self-motion through orientation of a hand-held wand were recorded. The influence of the perception of self-motion on postural kinematics differed depending upon the plane and complexity of visual motion. Postural behaviors generated through the perception of self-motion appeared to contain a confluence of the cortically integrated visual and vestibular signals and of other somatosensory inputs. This would suggest that spatial representation during motion in the environment is modified by both ascending and descending controls. We infer from these data that motion of the visual surround can be used as a therapeutic tool to influence posture and spatial orientation, particularly in more visually sensitive individuals following central nervous system (CNS) impairment.     

Attentional modulation in perception of visual motion events.

Identical visual targets moving across each other with equal and constant speed can be perceived either to bounce off or to stream through each other. This bistable motion perception has been studied mostly in the context of motion integration. Since the perception of most ambiguous motion is affected by attention, there is the possibility of attentional modulation occurring in this case as well. We investigated whether distraction of attention from the moving targets would alter the relative frequency of each percept. During the observation of the streaming/bouncing motion event in the peripheral visual field, visual attention was disrupted by an abrupt presentation of a visual distractor at various timings and locations (experiment 1; exogenous distraction of attention) or by the demand of an additional discrimination task (experiments 2 and 3; endogenous distraction of attention). Both types of distractions of attention increased the frequency of the bouncing percept and decreased that of the streaming percept. These results suggest that attention may facilitate the perception of object motion as continuing in the same direction as in the past.     

Visual search for a motion singleton among coherently moving distractors

In the current study, we tested whether search for a visual motion singleton presented among several coherently moving distractors can be more efficient than search for a motion stimulus presented with a single distractor. Under a variety of conditions, multiple spatially distributed and coherently moving distractors facilitated search for a uniquely moving target relative to a single-motion-distractor condition (Experiments 1, 3, and 4). Color coherencies among static distractors were not equally effective (Experiments 1 and 2). These results confirm that humans are highly sensitive to antagonistically directed motion signals in backgrounds compared with spatially more confined regions of visual images.     

Why do parallel cortical systems exist for the perception of static form and moving form?

This article analyzes computational properties that clarify why the parallel cortical systems V1----V2, V1----MT, and V1----V2----MT exist for the perceptual processing of static visual forms and moving visual forms. The article describes a symmetry principle, called FM symmetry, that is predicted to govern the development of these parallel cortical systems by computing all possible ways of symmetrically gating sustained cells with transient cells and organizing these sustained-transient cells into opponent pairs of on-cells and off-cells whose output signals are insensitive to direction of contrast. This symmetric organization explains how the static form system (static BCS) generates emergent boundary segmentations whose outputs are insensitive to direction of contrast and insensitive to direction of motion, whereas the motion form system (motion BCS) generates emergent boundary segmentations whose outputs are insensitive to direction of contrast but sensitive to direction of motion. FM symmetry clarifies why the geometries of static and motion form perception differ--for example, why the opposite orientation of vertical is horizontal (90 degrees), but the opposite direction of up is down (180 degrees). Opposite orientations and directions are embedded in gated dipole opponent processes that are capable of antagonistic rebound. Negative afterimages, such as the MacKay and waterfall illusions, are hereby explained as are aftereffects of long-range apparent motion. These antagonistic rebounds help to control a dynamic balance between complementary perceptual states of resonance and reset. Resonance cooperatively links features into emergent boundary segmentations via positive feedback in a CC loop, and reset terminates a resonance when the image changes, thereby preventing massive smearing of percepts. These complementary preattentive states of resonance and reset are related to analogous states that govern attentive feature integration, learning, and memory search in adaptive resonance theory. The mechanism used in the V1----MT system to generate a wave of apparent motion between discrete flashes may also be used in other cortical systems to generate spatial shifts of attention. The theory suggests how the V1----V2----MT cortical stream helps to compute moving form in depth and how long-range apparent motion of illusory contours occurs. These results collectively argue against vision theories that espouse independent processing modules. Instead, specialized subsystems interact to overcome computational uncertainties and complementary deficiencies, to cooperatively bind features into context-sensitive resonances, and to realize symmetry principles that are predicted to govern the development of the visual cortex.     

A computational feature binding model of human texture perception

We present a computational model for human texture perception which assigns functional principles to the Gestalt laws of similarity and proximity. Motivated by early vision mechanisms, in the first stage, local texture features are extracted by utilizing multi-scale filtering and nonlinear spatial pooling. In the second stage, features are grouped according to the spatial feature binding model of the competitive layer model (CLM; Wersing et al. 2001). The CLM uses cooperative and competitive interactions in a recurrent network, where binding is expressed by the layer-wise coactivation of feature-representing neurons. The Gestalt law of similarity is expressed by a non-Euclidean distance measure in the abstract feature space with proximity being taken into account by a spatial component. To choose the stimulus dimensions which allow the most salient similarity-based texture segmentation, the feature similarity metrics is reduced to the directions of maximum variance. We show that our combined texture feature extraction and binding model performs segmentation in strong conformity with human perception. The examples range from classical microtextures and Brodatz textures to other classical Gestalt stimuli, which offer a new perspective on the role of texture for more abstract similarity grouping.     

A revised analysis of the role of efference in motion perception

The analysis of motion perception historically has included efferent as well as afferent mechanisms to account for the perception of motion during eye movement. The application of efferent mechanisms to motion perception has been limited, however, by several illusions which are apparently inconsistent with the notion that oculomotor mechanisms contribute to motion perception. An alternative account is presented of the manner in which efference may contribute to the perception of motion. It is proposed that distinct smooth eye-movement systems contribute differentially to object motion perception. Specifically, activity in the smooth pursuit system gives rise to the perception of object motion, whereas activity in the smooth component of reflexive eye movements does not. Tracking of a moving object results in object motion perception as a result of efference in the pursuit system. However, the pursuit system may be activated to oppose the smooth component of reflexive eye movements in order to preserve fixation on a stationary object. In such cases neither the fixated object nor the eye is moving but illusory movement results from the efference in the pursuit system. A number of illusory movement phenomena are interpreted in terms of this model.     

Visual discrimination of texture

Julesz (1975) proposed a theory of texture discrimination, based on an order statistics principle, which states that no two textures can be perceptually discriminated if they have identical second-order statistics. The experiments reported here demonstrate that this principle is not adequate to predict visual texture discriminability. Both letter and dot micropatterns were used to create texture pairs that either differed or were identical with respect to secondorder statistics. The subject’s task was to decide which quadrant of an array contained a disparate texture. In Experiments 1, 2, and 3, when controlling for spatial overlap, texture pairs having identical second-order statistics were discriminated more quickly than similar texture pairs having different second-order statistics, in contradiction to the principle. Although a significant effect in the direction predicted by the order statistics principle was found in Experiment 4 for texture pairs created from the dot micropatterns, other factors, such as spatial overlap, border differences, and goodness of pattern, must also be considered in predicting texture discriminability.     

Temporal masking level differences for transients: Further evidence for a short-term integrator

Studies of binaural perception have indicated that subjects are able to use temporal information available in high-frequency regions of the spectrum to lateralize high-frequency waveforms but not to detect these waveforms in masking noise. The present experiments demonstrate that although high-frequency interaural difference cues are relatively ineffective in simultaneous and forward masking, they can be utilized in backward masking. In Experiment 1, large maskinglevel differences were found in backward masking for high-frequency transients presented either monaurally or with an interaural temporal delay. Experiments 2–4 examined fringe masking, effects of masker duration, and combined forward-backward masking for both high- and lowfrequency transients presented with interaural differences in phase and intensity. The results are interpreted as support for the view that the auditory system is organized into parallel shortand long-term integration systems specialized for processing transient and sustained aspects of acoustic stimulation. It is suggested that information from the two integrators is combined when analysis of interaural differences within each of the systems yields similar estimates of spatial location.