The effect of hand position and pattern motion on temporal order judgments

Subjects made temporal order judgments (TOJs) of tactile stimuli presented to the fingerpads. The subjects judged which one of two locations had been stimulated first. The tactile stimuli were patterns that simulated movement across the fingerpads. Although irrelevant to the task, the direction of movement of the patterns biased the TOJs. If the pattern at one location moved in the direction of the second location, the subjects tended to judge the first location as leading the second location. If the pattern moved in the opposite direction, that location was judged as trailing. In a series of experiments, the effect of the spatial position of the hands and fingers on TOJs and the perception of the direction of pattern movement were examined. Changing the position of the hands so that the patterns no longer moved directly toward each other reduced or eliminated the effect of motion on TOJs. In a variation of Aristotle's illusion, the moving patterns were presented to crossed and uncrossed fingers. The results indicated that, contrary to Aristotle's illusion, the subjects processed the moving patterns relative to an environmental framework, rather than to the local direction of motion on the fingerpads. Presenting the patterns to crossed hands produced results similar to those obtained with crossed fingers: The subjects processed the patterns according to an environmental framework.     

Discrimination of intentional and random motion paths by pigeons

Twelve pigeons (Columba livia) were trained on a go/no-go schedule to discriminate between two kinds of movement patterns of dots, which to human observers appear to be "intentional" and "non-intentional" movements. In experiment 1, the intentional motion stimulus contained one dot (a "wolf") that moved systematically towards another dot as though stalking it, and three distractors ("sheep"). The non-intentional motion stimulus consisted of four distractors but no stalker. Birds showed some improvement of discrimination as the sessions progressed, but high levels of discrimination were not reached. In experiment 2, the same birds were tested with different stimuli. The same parameters were used but the number of intentionally moving dots in the intentional motion stimulus was altered, so that three wolves stalked one sheep. Despite the enhanced difference of movement patterns, the birds did not show any further improvement in discrimination. However, birds for which the non-intentional stimulus was associated with reward showed a decline in discrimination. These results indicated that pigeons can discriminate between stimuli that do and do not contain an element that human observer see as moving intentionally. However, as no feature-positive effect was found in experiment 1, it is assumed that pigeons did not perceive or discriminate these stimuli on the basis that the intentional stimuli contained a feature that the non-intentional stimuli lacked, though the convergence seen in experiment 2 may have been an effective feature for the pigeons. Pigeons seem to be able to recognise some form of multiple simultaneously goal-directed motions, compared to random motions, as a distinctive feature, but do not seem to use simple "intentional" motion paths of two geometrical figures, embedded in random motions, as a feature whose presence or absence differentiates motion displays. Electronic Publication     

Effects of agency on movement interference during observation of a moving dot stimulus

Human movement performance is subject to interference if the performer simultaneously observes an incongruent action. It has been proposed that this phenomenon is due to motor contagion during simultaneous movement performance-observation, with coactivation of shared action performance and action observation circuitry in the premotor cortex. The present experiments compared the interference effect during observation of a moving person with observation of moving dot stimuli: The dot display followed either a biologically plausible or implausible velocity profile. Interference effects due to dot observation were present for both biological and nonbiological velocity profiles when the participants were informed that they were observing prerecorded human movement and were absent when the dot motion was described as computer generated. These results suggest that the observer's belief regarding the origin of the dot motion (human-computer generated) modulates the processing of the dot movement stimuli on their later integration within the motor system, such that the belief regarding their biological origin is a more important determinant of interference effects than the stimulus kinematics.     

The pigeon's discrimination of movement patterns (Lissajous figures) and contour-dependent rotational invariance

The ability of pigeons to discriminate complex motion patterns was investigated with the aid of moving Lissajous figures. The pigeons successfully learned to differentiate two successively presented cyclic trajectories of a single moving dot. This suggests that they can recognize a movement Gestalt when information about shape is minimal. They also quickly learned a new discrimination between moving-outline stimuli with repetitively changing contour patterns. Contrasting results were obtained when the dot or outline stimuli were axis-rotated through 90 degrees. Rotational invariance of pattern discrimination was clearly demonstrated only when moving contours were visible. Nevertheless, pigeons could discriminate the axis-orientation of a moving-dot or moving-outline pattern when trained to do so. Discrimination did not seem to depend on single parameters of motion but rather on the recognition of a temporally integrated movement Gestalt. The visual system of pigeons, as well as that of humans, may be well adapted to recognize the types of oscillatory movements that represent components of the motor behaviour shown by many living organisms.     

Additivity of retinal and pursuit velocity in the perceptions of depth and rigidity from object-produced motion parallax

Two psychophysical experiments were conducted to investigate the mechanism that generates stable depth structure from retinal motion combined with extraretinal signals from pursuit eye movements. Stimuli consisted of random dots that moved horizontally in one direction (ie stimuli had common motion on the retina), but at different speeds between adjacent rows. The stimuli were presented with different speeds of pursuit eye movements whose direction was opposite to that of the common retinal motion. Experiment 1 showed that the rows moving faster on the retina appeared closer when viewed without eye movements; however, they appeared farther when pursuit speed exceeded the speed of common retinal motion. The 'transition' speed of the pursuit eye movement was slightly, but consistently, larger than the speed of common retinal motion. Experiment 2 showed that parallax thresholds for perceiving relative motion between adjacent rows were minimum at the transition speed found in experiment 1. These results suggest that the visual system calculates head-centric velocity, by adding retinal velocity and pursuit velocity, to obtain a stable depth structure.     

Sensitivity to shearing and compressive motion in random dots

The sensitivity of the visual system to motion of differentially moving random dots was measured. Two kinds of one-dimensional motion were compared: standing-wave patterns where dot movement amplitude varied as a sinusoidal function of position along the axis of dot movement (longitudinal or compressional waves) and patterns of motion where dot movement amplitude varied as a sinusoidal function orthogonal to the axis of motion (transverse or shearing waves). Spatial frequency, temporal frequency, and orientation of the motion were varied. The major finding was a much larger threshold rise for shear than for compression when motion spatial frequency increased beyond 1 cycle deg-1. Control experiments ruled out the extraneous cues of local luminance or local dot density. No conspicuous low spatial-frequency rise in thresholds for any type of differential motion was seen at the lowest spatial frequencies tested, and no difference was seen between horizontal and vertical motion. The results suggest that at the motion threshold spatial integration is greatest in a direction orthogonal to the direction of motion, a view consistent with elongated receptive fields most sensitive to motion orthogonal to their major axis.     

The Perception of Self-Motion Induced by Peripheral Visual Information in Sitting and Supine Postures

The effects of speed and direction of a moving peripheral stimulus on the perception of self-motion were studied in sitting and supine postures. Observers sat or lay on their backs with one monitor on each side of their head. On the monitor screens, random dot patterns moved vertically or horizontally under three speed conditions. The latency of the onset of the induced self-motion was shorter under the high-speed condition than under the lower speed conditions. In the sitting posture, the latency was shorter when the patterns moved vertically than when they moved horizontally. In the supine posture, the latency depended neither on the physical nor on the egocentric verticality of the pattern motion. This shows that the effect of direction of moving patterns was not the same in the sitting posture and the supine posture. The results were explained by an informational difference of visual-vestibular interaction in each of these two postures.     

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.     

Visual search for motion-form conjunctions: is form discriminated within the motion system?

Motion-form conjunction search can be more efficient when the target is moving (a moving 45 degrees tilted line among moving vertical and stationary 45 degrees tilted lines) rather than stationary. This asymmetry may be due to aspects of form being discriminated within a motion system representing only moving items, whereas discrimination of stationary items relies on a static form system (J. Driver & P. McLeod, 1992). Alternatively, it may be due to search exploiting differential motion velocity and direction signals generated by the moving-target and distractor lines. To decide between these alternatives, 4 experiments systematically varied the motion-signal information conveyed by the moving target and distractors while keeping their form difference salient. Moving-target search was found to be facilitated only when differential motion-signal information was available. Thus, there is no need to assume that form is discriminated within the motion system.     

Matching cue size and task properties in exogenous attention

Exogenous attention is an involuntary, reflexive orienting response that results in enhanced processing at the attended location. The standard view is that this enhancement generalizes across visual properties of a stimulus. We test whether the size of an exogenous cue sets the attentional field and whether this leads to different effects on stimuli with different visual properties. In a dual task with a random-dot kinematogram (RDK) in each quadrant of the screen, participants discriminated the direction of moving dots in one RDK and localized one red dot. Precues were uninformative and consisted of either a large or a small luminance-change frame. The motion discrimination task showed attentional effects following both large and small exogenous cues. The red dot probe localization task showed attentional effects following a small cue, but not a large cue. Two additional experiments showed that the different effects on localization were not due to reduced spatial uncertainty or suppression of RDK dots in the surround. These results indicate that the effects of exogenous attention depend on the size of the cue and the properties of the task, suggesting the involvement of receptive fields with different sizes in different tasks. These attentional effects are likely to be driven by bottom-up mechanisms in early visual areas.     

Categorization of natural movements by pigeons: visual concept discrimination and biological motion

In three experiments, pigeons were exposed to a discriminated autoshaping procedure in which categories of moving stimuli, presented on videotape, were differentially associated with reinforcement. All stimuli depicted pigeons making defined responses. In Experiment 1, one category consisted of several different scenes of pecking and the other consisted of scenes of walking, flying, head movements, or standing still. Four of the 4 birds for which pecking scenes were positive stimuli discriminated successfully, whereas only 1 of the 4 for which pecking was the negative category did so. In the pecking-positive group, there were differences between the pecking rates in the presence of the four negative actions, and these differences were consistent across subjects. In Experiment 2, only the categories of walking and pecking were used; some but not all birds learned this discrimination, whichever category was positive, and these birds showed some transfer to new stimuli in which the same movements were represented only by a small number of point lights (Johansson's “biological motion” displays). In Experiment 3, discriminations between pecking and walking movement categories using point-light displays were trained. Four of the 8 birds discriminated successfully, but transfer to fully detailed displays could not be demonstrated. Pseudoconcept control groups, in which scenes from the same categories of motion were used in both the positive and negative stimulus sets, were used in Experiments 1 and 3. None of the 8 pigeons trained under these conditions showed discriminative responding. The results suggest that pigeons can respond differentially to moving stimuli on the basis of movement cues alone.     

Simultaneous encoding of direction at a local and global scale

Human observers can simultaneously encode direction information at two different scales, one local (an individual dot) and one global (the coherent motion of a field of dots distrisbuted over a 10°-diameter display). We assessed whether encoding global motion would preclude the encoding of a local trajectory component and vice versa. In the present experiments, a large number (100–150) of dots were randomly assigned directions in each frame from a uniform distribution of directions spanning a range of 160° to create global motion in a single direction (Williams & Sekuler, 1984). Amidst these background dots, 1 dot moved in a consistent direction (trajectory) for the duration of the display. The direction of this “trajectory dot” was similar to the mean direction of the distribution of directions determining the movement of the background dots. Direction discrimination for both the global motion and the trajectory was measured, using the method of constant stimuli, under precued and postcued partial report conditions. A low- or high-frequency 85-msec tone signaled which motion the subject was to judge. In the precue condition, the tone was presented 200 msecbefore the onset of the stimulus, whereas in the postcue condition, the tone was presented immediatelyafter the offset of the stimulus. Direction discrimination thresholds for both global and local motion in the postcued condition were not significantly different from those obtained in the precued condition. These results suggest that direction information for both global and local motion is encoded simultaneously and that the observer has access to either motion signal after the presentation of a stimulus.     

运动空间定向判断中的方向偏差及飞行惯性

模拟客体起飞和降落运动,探讨飞行场景中不同运动位置、不同意义客体和运动方向下个体运动空间定向判断能力。结果表明：(1)对降落运动轨迹的判断正确率显著低于起飞运动;(2)无意义客体偏高轨迹的判断正确率显著小于偏低轨迹,表现出方向偏差;(3)飞行场景影响方向偏差的表现形式,当飞机降落运动时,易将偏低路径判断为与预设轨迹相同,而飞机起飞运动时,易将偏高路径判断为相同,表明降落时飞机被知觉为会向斜下方越飞越低,而起飞时飞机会向斜上方越飞越高,表现出飞行惯性。结论：运动空间定向判断受到重力表征及个体知识经验等共同影响,具有认知可渗透性。     

运动空间定向判断中的方向偏差及飞行惯性

模拟客体起飞和降落运动,探讨飞行场景中不同运动位置、不同意义客体和运动方向下个体运动空间定向判断能力。结果表明：(1)对降落运动轨迹的判断正确率显著低于起飞运动;(2)无意义客体偏高轨迹的判断正确率显著小于偏低轨迹,表现出方向偏差;(3)飞行场景影响方向偏差的表现形式,当飞机降落运动时,易将偏低路径判断为与预设轨迹相同,而飞机起飞运动时,易将偏高路径判断为相同,表明降落时飞机被知觉为会向斜下方越飞越低,而起飞时飞机会向斜上方越飞越高,表现出飞行惯性。结论：运动空间定向判断受到重力表征及个体知识经验等共同影响,具有认知可渗透性。     

Unexpected changes in direction of motion attract attention

Under some circumstances, moving objects capture attention. Whether a change in the direction of a moving object attracts attention is still unexplored. We investigated this using a continuous tracking task. In Experiment 1, four grating patches changed smoothly and semirandomly in their positions and orientations, and observers attempted to track the orientations of two of them. After the stimuli disappeared, one of the two target gratings was queried and observers reported its orientation; hence direction of the gratings' motion across the screen was an irrelevant feature. Despite the irrelevance of its motion, when the nonqueried grating had collided with an invisible boundary within the last 200 msec of the trial, accuracy reporting the queried grating was worse than when it had not. Attention was likely drawn by the unexpected nature of these changes in direction of motion, since the effect was eliminated when the boundaries were visible (Experiment 2). This tendency for unexpected motion changes to attract attention has important consequences for the monitoring of objects in everyday environments.     

Symmetry and elongation of objects influence perceived direction of translational motion

Five experiments were conducted to examine how perceived direction of motion is influenced by aspects of shape of a moving object such as symmetry and elongation. Random polygons moving obliquely were presented on a computer screen and perceived direction of motion was measured. Experiments 1 and 2 showed that a symmetric object moving off the axis of symmetry caused motion to be perceived as more aligned with the axis than it actually was. However, Experiment 3 showed that motion did not influence perceived orientation of symmetry axis. Experiment 4 revealed that symmetric shapes resulted in faster judgments on direction of motion than asymmetric shapes only when the motion is along the axis. Experiment 5 showed that elongation causes a bias in perceived direction of motion similar to effects of symmetry. Existence of such biases is consistent with the hypothesis that in the course of evolution, the visual system has been adapted to regularities of motion in the animate world.     

Visual movement perception in deaf and hearing individuals

A number of studies have investigated changes in the perception of visual motion as a result of altered sensory experiences. An animal study has shown that auditory-deprived cats exhibit enhanced performance in a visual movement detection task compared to hearing cats (Lomber, Meredith, & Kral, 2010). In humans, the behavioural evidence regarding the perception of motion is less clear. The present study investigated deaf and hearing adult participants using a movement localization task and a direction of motion task employing coherently-moving and static visual dot patterns. Overall, deaf and hearing participants did not differ in their movement localization performance, although within the deaf group, a left visual field advantage was found. When discriminating the direction of motion, however, deaf participants responded faster and tended to be more accurate when detecting small differences in direction compared with the hearing controls. These results conform to the view that visual abilities are enhanced after auditory deprivation and extend previous findings regarding visual motion processing in deaf individuals.     

Motion capture depends on signal strength

When flickering dots are superimposed onto a drifting grating, the dots appear to move coherently with the grating. In this study we examine: (i) how the perceived direction of a compound stimulus composed of superimposed grating and dots, moving in opposite directions with equal speeds, is influenced by the relative strength of the motion signals; (ii) how the perceived speed of a compound stimulus composed of superimposed grating and dots, moving in the same direction but at different speeds, is influenced by the relative strength of the motion signals; and (iii) whether this stimulus is discriminable from its metameric speed match. Dot signal strength was manipulated by using different proportions of signal dots in noise and different dot lifetimes. Both the perceived direction and speed of these compound stimuli depended upon the relative motion-signal strengths of the grating and the dots. Those compound stimuli that appeared coherent were not discriminable from the speed-matched metameric compound stimuli. When the signals were completely integrated into a coherent compound stimulus, the local motion signals were no longer perceptually available, though both contributed to the global percept. These data strongly support a weighted-combination model where the relative weights depend on signal strength, instead of a winner-takes-all model.     

Numerical acuity of fish is improved in the presence of moving targets,but only in the subitizing range

There is controversy in comparative psychology about whether on the one hand non-symbolic number estimation of small (≤4) and large numbers involves a single mechanism (an approximate number system), or whether on the other hand enumeration of the numbers 1–4 is accomplished by a separate mechanism, an object tracking system. To date, support for the latter hypothesis has come only from the different ratio-dependency of performance seen in the two numerical ranges, a reading that has been criticized on several grounds. In humans, the two-system hypothesis is supported by evidence showing that manipulation of the physical properties of the stimuli (e.g., the motion of the items) has dissimilar effects on small- and large-number discrimination. In this research, we studied this effect on guppies. Initially, fish were trained to simultaneously discriminate two numerical contrasts having the same easy ratio (0.50): one in the small-number (2 vs. 4) range and one in the large-number (6 vs. 12) range. Half of the fish were presented with moving items; the other half were shown the same stimuli without motion. Fish were then subjected to non-reinforced probe trials in the presence of a more difficult ratio (0.75: 3 vs. 4 and 9 vs. 12). Under both static and moving conditions, the fish significantly discriminated 6 versus 12, but not 9 versus 12 items. As regards small numbers, both groups learned to discriminate a 0.50 ratio, but only fish tested with moving stimuli also discriminated 3 and 4 items. This differential effect suggests that fish may possess two separate systems for small- and large-number discrimination.     

The locus of spatial attention during the temporal integration of visual memories and visual percepts

Temporal integration is a process by which two serially presented visual stimuli are mentally integrated to form a composite representation. In the present research, we explored how spatial selective attention is used during the delay separating stimuli, in order to determine the contents of spatial working memory in this task. A two-task situation was created. On the primary task, two dot arrays were serially presented within a grid, leaving one space empty, which subjects identified. On the secondary task, instead of the second array, a discrimination probe was presented. Integration accuracy increased through delays of 1,500 msec, revealing an estimate of the time required to form an optimal memory trace for integration. Once the memory trace was formed (but not before), response time to the probe was faster if it was presented in a location previously occupied by a dot from Array 1. This indicates that during the delay separating the arrays, the subjects assigned spatial attention to the locations occupied by the first array and actively maintained the leading array in working memory. Implications for theories of visual processing and memory are discussed.