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PubMed1995

Spatial-gradient limit on perception of multiple motion.

Motion is perceived whenever a subject is presented with an appropriate spatiotemporal visual pattern. Like many other visual tasks, motion perception involves both local and global processing, and thus might be subject to the well-known paradox that arises from the fact that local features and observations form the basis for global perception, but sometimes this global percept can not be easily derived from any single local observation, as is best exemplified by the aperture problem. Globally, dual (transparent) motion can be readily perceived. Spatial limits on the local ability to perceive multiple motion are sought. By using the framework of apparent motion, it is found that dual, orthogonally oriented motion can be perceived only when the dots that constitute the two motions are separated by some spatial limit. For short-range apparent motion, the limit is found to be comparable to D(max), and the visual system cannot perceive more than a single coherent motion in a local "patch" of radius D(max). It was also found that this spatial limit on local-motion perception is not constant, but depends linearly on the spatial organisation of the stimuli, and vanishes for stimuli having reverse contrast. The lower bound on the ability to perceive multiple motion is compared with some well-known bounds in stereopsis, and a cortical columnar architecture that might account for it is proposed.

Adult↗
PubMed1993

The interaction of luminance, velocity, and shape information in the perception of motion transparency, coherence, and non-rigid motion.

The perception of luminance transparency for superimposed patterns depends on how luminance, figural, and topological conditions are simultaneously satisfied. Motion transparency or coherence for two superimposed patterns, which correspond to the perception of both patterns moving across one another or to the perception of compound motion of the regions of pattern intersection, depends on the relation between the local velocity, luminance, and shape information. This study analyzes how luminance, shape, and local velocity interact in the perception of motion transparency and coherence. Psychophysical experiments done with sinusoidally modulated bar patterns are presented which show that the perception of motion transparency or coherence can be described as the result of the interaction of two integration modules: the velocity-luminance and the velocity-shape processes. The velocity-luminance process describes the integration of the local velocity with luminance information. When the luminance transparency rules are satisfied this process always generates the perception of motion transparency independently of the shape or contour information. On the other hand, when the luminance transparency rules are violated one can either perceive motion coherence or non-rigid motion; one perceives motion coherence when the patterns have small or zero amplitude, and non-rigid motion when the patterns have large amplitude. The velocity-shape process describes the integration of local velocity with shape information, and this depends on the relation between the error in the extraction of the local velocity and the magnitude of the contour amplitude. As a result of these experiments it is conjectured that the velocity-luminance and the velocity-shape processes do interact constructively or destructively. The constructive interaction occurs when the luminance transparency rules are satisfied. The destructive interaction occurs when the luminance transparency rules are violated, and such that, although the patterns contain sufficient shape information to solve the aperture problem and therefore generate the perception of motion transparency, one perceives non-rigid motion. This shows that global information describing the stratification of superimposed patterns can affect the integration of local velocity information with, for example, shape information, and this is not described by current motion theories.

Form Perception↗
PubMed2000

Blindness to form from motion despite intact static form perception and motion detection.

We studied the motion perception, including form and meaning generated by motion, in a hemianopic patient who also had visual perceptual impairments in her seeing hemifield as a result of a lesion in ventral extrastriate cortex. She was unable to recognise 2- or 3-dimensional forms, and even borders, generated by motion alone, failed to recognise mimed actions or the Johannson 'biological motion' display, and ceased to recognise people well-known to her when they moved. Her performance with static displays, although impaired, could not explain her inability to perceive shape or derive meaning from moving displays. Unlike a motion-blind patient, she can still see and describe the motion, with the exception of second-order motion, but not what it creates or represents.

Aged↗
PubMed2005

Perception of chromatic motion requires luminance interaction.

There is an ongoing debate related to whether chromatic motion perception arises as a consequence of a chromatic signal only (eg Wandell et al 1999 Neuron 24 901-909) or a signal that is essentially based on luminance processes (luminance artifacts) (Mullen et al 2003 Vision Research 43 1235-1247). These two views conform to the idea that colour and luminance processes are physiologically independent (Livingstone and Hubel 1988 Science 240 740-749), but according to other reports many primary cortical 'V1' cells respond to both colour and luminance contrast (eg Vidyasagar et al 2002 European Journal of Neuroscience 16 945-956). A psychophysical task was designed to test whether possible interaction between luminance and chromatic contrast could account for perception of chromatic motion. It is shown that subjects respond in a manner that reflects involvement of both processes.

Color Perception↗
PubMed1998

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.

Attention↗
PubMed1987

Cooperative phenomena in the perception of motion direction.

A percept of global coherent motion can result from the combination of many different localized motion vectors. We report here evidence of hysteresis in the perception of this global motion, obtained with random-dot cinematograms. The hysteresis characteristics are relatively robust with respect to changes in dot density, display area, and location. Changing the directional content of the stimulus, however, did alter the hysteresis profile in a manner consistent with a model incorporating cooperative interactions among direction-selective motion mechanisms. Our results lend further support to a cooperative interpretation of motion results lend further support to a cooperative interpretation of motion perception in random-dot cinematograms.

Humans↗
PubMed2000

Perception of apparent motion is related to the neural activity in the human extrastriate cortex as measured by magnetoencephalography.

To determine the neural correlate of apparent motion perception, we measured magnetic responses to visual stimuli in apparent motion and compared the results with subjective rating of the quality of perceived motion with varied stimulus timing. The latency of the magnetic response was about 150 ms, and its origin was estimated to be in the occipito-parieto-temporal junction. The strength of the first component in the response varied with the stimulus timing, the maximum value being at the interval 0. The change could not be explained by the simple summation of onset and offset responses and this value was related to the subjective rating of quality (smoothness) of motion measured of the stimulus. Results indicate there is a localized cortical region of neural activity which is closely related to the subjective assessment of quality of perceived motion.

Adult↗
PubMed2003

The effect of object and event orientation on perception of biological motion.

Detection and recognition of point-light walking is reduced when the display is inverted, or turned upside down. This indicates that past experience influences biological motion perception. The effect could be the result of either presenting the human form in a novel orientation or presenting the event of walking in a novel orientation, as the two are confounded in the case of walking on feet. This study teased apart the effects of object and event orientation by examining detection accuracy for upright and inverted displays of a point-light figure walking on his hands. Detection of this walker was greater in the upright display, which had a familiar event orientation and an unfamiliar object orientation, than in the inverted display, which had a familiar object orientation and an unfamiliar event orientation. This finding supports accounts of event perception and recognition that are based on spatiotemporal patterns of motion associated with the dynamics of an event.

Adult↗
PubMed2004

Perception of apparent motion in depth: a high-density electrical mapping study in humans.

We evaluated brain activity using 64-channel visual evoked potentials (VEPs) while subjects perceived apparent motion in depth. Checkerboard patterns (CBPs) within small and large circles were presented in turn as experimental conditions. Motion in depth was perceived when the CBP in the large circle was coarser than in the small circle; when coarseness did not change, no motion in depth was perceived. As control conditions only fine or coarse CBPs were presented. We used ANOVA to compare VEPs associated with experimental vs. control conditions and with coarse vs. fine CBPs. Negative potentials at a latency near 190 ms showed statistically significant interactions between these comparisons in the right lateral occipital and posterior parietal areas when apparent motion in depth was perceived. This suggests that higher tiers of the dorsal stream mediate this motion perception.

Adult↗
PubMed1990

The relationship between visual persistence and event perception in bistable motion display.

Observers viewed two alternating frames, each consisting of three rectangular bars displaced laterally by one cycle in one frame with respect to the other. At long interframe intervals (IFIs) observers perceived a group of three bars moving as a whole (group motion), and at short IFIs the overlapping elements in the two frames appeared stationary, while the third element appeared to move from one end of the display to the other (element motion). The upper temporal limit for perceiving element motion was reduced when bars with blurred edges were used and when either frame duration or bar size was increased. However, when inner and outer elements had different sizes, the element motion percept was dominant up to 230 ms IFI. These findings may be interpreted in terms of spatial tuning of motion mechanisms involved in the perception of bistable apparent motion.

Attention↗
PubMed1990

The role of directionally selective neurons in the perception of global motion.

Dynamic random dot targets consisting of many localized motion vectors have been used to study the pooling of local motion signals into a global motion percept (Williams and Sekuler, 1984). In such displays, the dots are displaced with a constant step size and the direction of motion for each dot is chosen at random from a specified distribution. When the distribution extends over 360 deg, the display consists only of local random motion of individual dots and no coherent motion is reported. However, when the distribution is less than 360 deg (biased), the stimulus appears to flow in a single direction. We examined the effects of reducing the number of directionally selective (DS) cortical neurons on this integration process. Normal cats and cats with severely reduced proportions of DS neurons were trained on 2 direction discrimination tasks. The discrimination of opposite directions was examined while varying either the range of directions of local motion, or the proportion of dots moving with biased distribution. When all dots in the display were directionally biased, cats with reduced numbers of DS neurons performed the task as well as normal cats and humans (threshold range: 280-320 deg). However, when the proportion of biased dots decreased, these animals had severe deficits. Thus, in the absence of noise, even a very small number of DS neurons can perform spatial pooling of local directional signals, and support normal discrimination of opposite directions. However, a full complement of directional detectors appears necessary when the motion signal is masked by noise. The discrimination of small differences in direction revealed far more severe deficits, even when all the dots in the display were directionally biased (no noise).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed2005

Attention modulates perception of transparent motion.

Human observers can extract a given motion direction from sets of random dots moving simultaneously in two or more directions in the same region of the visual field, a phenomenon referred to as motion transparency. As a necessary condition for separating transparent motion directions, low level encoding of local motion signals must generate frequency distributions of local directions with separable peaks corresponding to these directions--this process would be constrained by local stimulus attributes and the properties of local motion detectors. Furthermore, a representation of multiple directions is needed for simultaneous retrieval of several directions in a psychophysical task--this operation would be limited by higher level processes, such as attention selecting a particular direction to rise into awareness. Preliminary observations suggest that the number of directions that can be seen simultaneously is rather limited and the question arises whether this could be related to limitations of low-level encoding or higher level representations. To study specifically the effect of attention on transparent motion perception, observers were presented with sets of dots moving coherently in a variable number of directions, and were asked after the presentation whether one particular direction was present in the set. When the direction of motion was not known before stimulus onset (uncued condition), observers detected a particular motion direction among no more than 3 other directions. When direction of motion was indicated prior to stimulus onset (precued condition), however, this limit increased up to 6 directions. This attentional effect showed some inter-individual variability and appeared to benefit from spatiotemporal integration of the motion signals. A corresponding effect became apparent when observers were tested in the same paradigm whether they could separate two motion directions with variable angular difference between them. In the precued condition a typical minimum direction difference was about 60 degrees, whereas in the uncued condition this was about 120 degrees, suggesting that the performance in detecting one direction in a multiple direction stimulus might be limited by the ability to separate adjacent motion directions. This pattern of results suggests that attention can reliably improve transparent motion processing by affecting the separability of directional signals in low level encoding mechanisms.

Attention↗
PubMed1994

Perception of apparent motion between dissimilar gratings: spatiotemporal properties.

What determines the strength of texture-defined apparent motion perception when the stimulus has no net directional energy in the Fourier domain? In a previous paper [Werkhoven, Sperling & Chubb (1993) Vision Research, 33, 463-485] we demonstrated the counterintuitive finding that the correspondence in spatial frequency and in modulation amplitude between neighboring patches of texture in a spatiotemporal motion path are irrelevant to motion strength. Instead, we found strong support for what we call a single channel or one-dimensional motion computation: a simple nonlinear transformation of the image, followed by standard motion analysis. Here, we further studied the dimensionality of the motion computation in a parameter space that includes texture orientation and stimulus display rate in addition to texture spatial frequency and modulation amplitude. We used ambiguous motion displays in which one motion path, consisting of patches of nonsimilar texture, competes with another motion path comprised entirely of similar texture patches. The data show that motion between dissimilar patches of texture that are orthogonally oriented, have a two octave difference in spatial frequency and differ 50% in modulation amplitude can easily dominate motion between similar patches of texture. A single channel accounts for more than 70% of texture-from-motion strength for the parameter space examined and this channel is invariant for stimulus display rates varying over a four-fold range.

Humans↗
PubMed1996

Optical blur and the perception of global coherent motion in random dot cinematograms.

We evaluated the effect of +3.25 dioptres of optical blur on the discrimination of motion direction in random dot cinematograms. Dot displacement between frames varied from 2.1 to 63' of visual angle while the temporal interval was held constant. Optical blur worsened discrimination in three normal subjects at displacements below 16', but improved discrimination at displacements of 21' or more. In a second experiment, two subjects viewed equivalent velocity stimuli constructed with different combinations of temporal interval and spatial displacement. Results showed that the effect of blur was specific to displacement and not velocity. Furthermore, varying the dot density of the display showed that the effect of blur correlated with dot displacement and not the probability of dot mismatches. Since optical blur attenuates high spatial frequencies, this suggests that high spatial frequencies are important for motion perception when dot displacements are less than 16' to 21', but reduce motion perception at larger dot displacements. The use of random dot cinematograms in populations must take into account stimulus displacement and optical causes of reduced spatial acuity.

Contrast Sensitivity↗
PubMed2006

Visual perception of biological motion by form: a template-matching analysis.

Biological motion perception is referred to as the ability to recognize a moving human figure from no more than a few moving point lights. Such point-light stimuli contain limited form information about the shape of the body and local image motion signals from the moving points. The contributions of form and motion to the vivid perception of point-light displays are subject to controversy in the discussion. While some studies claim that local motion signals are critical, others emphasize the role of global form cues. Here, we present a template-matching approach to investigate the role of global form analysis. We used a template-matching method that derives biological motion exclusively from form information. The algorithm used static postures monitored from walking humans as stored templates. We compared the simulation results to psychophysical experiments with the commonly used point-light walker and a variant point-light walker with near-absent local motion signals. The common result in all experiments was a high correlation between simulation results and psychophysical data. The results show that the limited form information in point-light stimuli might be sufficient to perceive biological motion. We suggest that it is possible for humans to extract the sparse form information in point-light walkers and to use it to perceive biological motion by integrating dynamic form information over time.

Discrimination, Psychological↗
PubMed2006

Depth separation between foreground and background on visually induced perception of self-motion.

A uniformly moving visual pattern can induce observer's self-motion perception in the opposite direction (vection), and an additional static stimulus can modulate (facilitate or inhibit) the strength of it. The present study was designed to investigate the effects of stimulus depth order and the depth distances of the visual stimulus on the inhibition and facilitation of vection caused by the additional static stimulus, measuring duration and estimated magnitude of vection as indices of vection strength. Analysis of this psychophysical experiment with four participants indicated that the static foreground presented in front of the moving pattern can facilitate vection, whereas the static background inhibits it (Duration: F1,3= 12.06, p<.05; Estimation: F1,3= 13.87, p<.05). Furthermore, the depth distances from the observer or the depth separation between the foreground and the background did not affect the self-motion perception (F2,6 < 1.0 for duration and estimation).

Adult↗