Motion and position shifts induced by the double-drift stimulus are unaffected by attentional load

The double-drift stimulus produces a strong shift in apparent motion direction that generates large errors of perceived position. In this study, we tested the effect of attentional load on the perceptual estimates of motion direction and position for double-drift stimuli. In each trial, four objects appeared, one in each quadrant of a large screen, and they moved upward or downward on an angled trajectory. The target object whose direction or position was to be judged was either cued with a small arrow prior to object motion (low attentional load condition) or cued after the objects stopped moving and disappeared (high attentional load condition). In Experiment 1, these objects appeared 10° from the central fixation, and participants reported the perceived direction of the target’s trajectory after the stimulus disappeared by adjusting the direction of an arrow at the center of the response screen. In Experiment 2, the four double-drift objects could appear between 6 ° and 14° from the central fixation, and participants reported the location of the target object after its disappearance by moving the position of a small circle on the response screen. The errors in direction and position judgments showed little effect of the attentional manipulation—similar errors were seen in both experiments whether or not the participant knew which double-drift object would be tested. This suggests that orienting endogenous attention (i.e., by only attending to one object in the precued trials) does not interact with the strength of the motion or position shifts for the double-drift stimulus.     

Motion illusion reveals fixation stability of karate athletes

To investigate the effect of smooth pursuit effort against optokinetic nystagmus (OKN) on the magnitude of induced motion, we measured the magnitude of induced motion and eye movements of karate athletes and novices. In Experiment 1, participants were required to pursue a horizontally moving fixation stimulus against a vertically moving inducing stimulus and to point at the most distorted position of the perceived pathway of the fixation stimulus. In Experiments 2 and 3, participants were presented with the inducing stimulus with or without a static fixation stimulus. Experiments 1 and 2 showed a larger magnitude of induced motion and more stable fixation for the athletes than for the novices. Experiment 3 showed no difference in eye movements between the two groups. These results suggest that the magnitude of induced motion reflects fixation stability that may have been strengthened in karate athletes through their experience and training.     

The Simon effect and visual motion

Summary S-R compatibility and Simon effects were studied for real visual motion. In Experiment 1, two small stimulus lights were constantly visible, 5° to the left and right of fixation; after a random delay, one began to move at 2°/s. In Experiment 2, a single stimulus light moving at 2°/s suddenly appeared 5° to the left or right of fixation, i. e., motion onset and stimulus onset coincided. In both experiments, subjects responded by a key press with their left or right index finger as soon as they detected motion. In Condition A responses were made to the position (left or right) from which the motion started, irrespective of its direction (position compatibility); in Condition B responses were made to the direction of motion (leftward or rightward) irrespective of whether motion started to the left or to the right of fixation (direction compatibility). The results show strong compatibility effects for both position and direction of motion in both experiments. A Simon effect, however, occurred only when position was task irrelevant in Experiment 1; no Simon effect was found in Experiment 2. The data only partly confirm previous results obtained with apparent motion. The selective lack of a Simon effect supports the integrated model of Umiltá and Nicoletti (1992), which requires orienting of attention for the Simon effect to occur. It is specifically assumed that this attention-orienting is triggered only by the saccade program and does not extend to the pursuit program that is initiated by smooth stimulus motion.     

Immediate and delayed recognition of sequentially presented random shapes.

Two experiments tested whether short-term memory accounts for the recency effect observed with rapid sequential presentation of nonverbal stimuli. Four random shapes were presented sequentially (with no interstimulus interval) on each trial at rates of 150 msec, 250 msec, 500 msec, and 1,000 msec per stimulus. Subsequent recognition varied positively with exposure duration, ranging from 57% at 150 msec to 77% at 1,000 msec. Two serial position effects were observed: a slight decrease in recognition accuracy for the first stimulus in each sequence and a large increase in recognition for the last stimulus in each sequence. The recency effect was not altered by an intervening 30-sec delay, an intervening 30-sec copying task, or an intervening 30-sec copying and counting task. Since neither visual nor verbal distractors altered recognition accuracy, it was suggested that all shapes were processed directly into long-term memory storage. It also was hypothesized that long-term storage of a nonverbal stimulus requires identification of a distinctive feature of the stimulus and that this process may continue for a brief period after actual stimulus offset.     

Conditioned reinforcement in second-order schedules

Pigeons responded under a schedule in which food was presented only after a fixed number of fixed-interval components were completed. Two such second-order schedules were studied: under one, 30 consecutive 2-min fixed-interval components were required; under the other, 15 consecutive 4-min fixed-interval components were required. Under both schedules, when a 0.7-sec stimulus light was presented at completion of each fixed interval, positively accelerated responding developed in each component. When no stimulus change occurred at completion of each fixed interval, relatively low and constant rates of responding prevailed in each component; a similar result was obtained when a 0.7-sec stimulus change occurred at completion of each fixed interval except the one which terminated with primary reinforcement. The 0.7-sec stimulus correlated with food delivery was an effective conditioned reinforcer in maintaining patterns of responding in fixed-interval components despite low average frequencies of food reinforcement.     

The development of depth perception from motion parallax in infancy

North Dakota State University, Fargo, North Dakota Little is known about infants' perception of depth from motion parallax, even though it is known that infants are sensitive both to motion and to depth-from-motion cues at an early age. The present experiment assesses whether infants are sensitive to the unambiguous depth specified by motion parallax and, if so, when this sensitivity first develops. Eleven infants were followed longitudinally from 8 to 29 weeks. Infants monocularly viewed a translating Rogers and Graham (1979) random-dot stimulus, which appears as a corrugated surface to adult observers. Using the infant-control habituation paradigm, looking time was recorded for each 10-sec trial until habituation, followed by two test trials: one using a depth-reversed and one using a flat stimulus. Dishabituation results indicate that infants may be sensitive to unambiguous depth from motion parallax by 16 weeks of age. Implications for the developmental sequence of depth from motion, stereopsis, and eye movements are discussed.     

Colour and spatial cueing in low-prevalence visual search

People are able to judge the current position of occluded moving objects. This operation is known as motion extrapolation. It has previously been suggested that motion extrapolation is independent of the oculomotor system. Here we revisited this question by measuring eye position while participants completed two types of motion extrapolation task. In one task, a moving visual target travelled rightwards, disappeared, then reappeared further along its trajectory. Participants discriminated correct reappearance times from incorrect (too early or too late) with a two-alternative forced-choice button press. In the second task, the target travelled rightwards behind a visible, rectangular occluder, and participants pressed a button at the time when they judged it should reappear. In both tasks, performance was significantly different under fixation as compared to free eye movement conditions. When eye movements were permitted, eye movements during occlusion were related to participants' judgements. Finally, even when participants were required to fixate, small changes in eye position around fixation (<2°) were influenced by occluded target motion. These results all indicate that overlapping systems control eye movements and judgements on motion extrapolation tasks. This has implications for understanding the mechanism underlying motion extrapolation.     

The role of perception in the mislocalization of the final position of a moving target

The judged final position of a moving stimulus has been suggested to be shifted in the direction of motion because of mental extrapolation (representational momentum). However, a perceptual explanation is possible: The eyes overshoot the final position of the target, and because of a foveal bias, the judged position is shifted in the direction of motion. To test this hypothesis, the authors replicated previous studies, but instead of having participants indicate where the target vanished, the authors probed participants' perceptual focus by presenting probe stimuli close to the vanishing point. Identification of probes in the direction of target motion was more accurate immediately after target offset than it was with a delay. Another experiment demonstrated that judgments of the final position of a moving target are affected by whether the eyes maintain fixation or follow the target. The results are more consistent with a perceptual explanation than with a memory account.     

Varying temporal placement of an added stimulus in a fixed-interval schedule

One paradigm for exploring stimulus effects on behavior is defined for steady state experiments. The paradigm is illustrated by a 60-sec fixed-interval reinforcement schedule wherein a 6-sec light is introduced into each interval. The temporal relation of this stimulus to the reinforcer is the independent variable that is systematically explored. Two experiments studied this temporal relation under two parametric conditions: (a) when the 6-sec light occurs once in each 60-sec interval, (b) when the 6-sec light occurs twice in each interval, the second time always during the 6 sec immediately preceding the reinforcer. Functions are presented showing the effect of the 6-sec light on responding at all points in the fixed-interval.     

Do common systems control eye movements and motion extrapolation?

People are able to judge the current position of occluded moving objects. This operation is known as motion extrapolation. It has previously been suggested that motion extrapolation is independent of the oculomotor system. Here we revisited this question by measuring eye position while participants completed two types of motion extrapolation task. In one task, a moving visual target travelled rightwards, disappeared, then reappeared further along its trajectory. Participants discriminated correct reappearance times from incorrect (too early or too late) with a two-alternative forced-choice button press. In the second task, the target travelled rightwards behind a visible, rectangular occluder, and participants pressed a button at the time when they judged it should reappear. In both tasks, performance was significantly different under fixation as compared to free eye movement conditions. When eye movements were permitted, eye movements during occlusion were related to participants' judgements. Finally, even when participants were required to fixate, small changes in eye position around fixation (<2°) were influenced by occluded target motion. These results all indicate that overlapping systems control eye movements and judgements on motion extrapolation tasks. This has implications for understanding the mechanism underlying motion extrapolation.     

Perceived shifts of flashed stimuli by visible and invisible object motion

Perceived positions of flashed stimuli can be altered by motion signals in the visual field-position capture (Whitney and Cavanagh, 2000 Nature Neuroscience 3 954-959). We examined whether position capture of flashed stimuli depends on the spatial relationship between moving and flashed stimuli, and whether the phenomenal permanence of a moving object behind an occluding surface (tunnel effect; Michotte 1950 Acta Psychologica 7 293-322) can produce position capture. Observers saw two objects (circles) moving vertically in opposite directions, one in each visual hemifield. Two horizontal bars were simultaneously flashed at horizontally collinear positions with the fixation point at various timings. When the movement of the object was fully visible, the flashed bar appeared shifted in the motion direction of the circle. But this position-capture effect occurred only when the bar was presented ahead of or on the moving circle. Even when the motion trajectory was covered by an opaque surface and the bar was flashed after complete occlusion of the circle, the position-capture effect was still observed, though the positional asymmetry was less clear. These results show that movements of both visible and 'hidden' objects can modulate the perception of positions of flashed stimuli and suggest that a high-level representation of 'objects in motion' plays an important role in the position-capture effect.     

The role of uncertainty in the systematic spatial mislocalization of moving objects

It only makes sense to talk about the position of a moving object if one specifies the time at which its position is of interest. The authors here show that when a flash or tone specifies the moment of interest, subjects estimate the moving object to be closer to where it passes the fixation point and further in its direction of motion than it really is. The authors propose that these biases arise from a combination of a large temporal uncertainty, a temporal asymmetry related to sampling the moving object's position, and a bias toward believing that one is looking at what one sees.     

Perceptual organization of moving stimuli modulates the flash-lag effect

When a visual stimulus is flashed at a given location the moment a second moving stimulus arrives at the same location, observers report the flashed stimulus as spatially lagging behind the moving stimulus (the flash-lag effect). The authors investigated whether the global configuration (perceptual organization) of the moving stimulus influences the magnitude of the flash-lag effect. The results indicate that a flash presented near the leading portion of a moving stimulus lags significantly more than a flash presented near the trailing portion. This result also holds for objects consisting of several elements that group to form a unitary percept of an object in motion. The present study demonstrates a novel interaction between the global configuration of moving objects and the representation of their spatial position and may provide a new and useful tool for the study of perceptual organization.     

There is no induced motion at near-threshold velocities

Duncker's classic experiments on induced motion at near-threshold velocities were based on the assumption that movement of one stimulus relative to the other (object-relative) is perfectly detected while it remains completely impossible to identify which of the two stimuli is moving (subject-relative). In the present experiments it is shown that the threshold areas of object-relative and subject-relative movement are largely overlapping. Consequently Dunker's assumption cannot be fulfilled: whenever object-relative movement is well detectable accuracy of detecting subject-relative motion will also be over 50%. In four additional experiments it is shown that the well-established effects of fixation, stimulus size and enclosure on induced motion are to be interpreted as effects of these variables on the detection of subject-relative movement: the so-called induction phenomena occured only when accuracy was over 50%.     

Effects on responding of mixed and multiple schedules of signalled and unsignalled response-dependent electric-shock delivery

Responding in two rats was maintained under mixed and multiple variable-interval 35-sec variable-interval 35-sec food delivery schedules. Similar rates and patterns of responding occurred in each component of the two schedules. Mixed and multiple variable-interval 65-sec variable-interval 65-sec schedules of response-dependent shock delivery were super-imposed on the mixed and multiple baseline food schedules, respectively. In one component, a 5-sec stimulus was presented on the average of once every 65 sec. Offset of the stimulus arranged that the next response would produce shock. In the other component, no stimulus was presented during the 5-sec period. The mixed schedule of signalled and unsignalled dependent shock delivery yielded similar degrees of response suppression in each component, but the multiple schedule of shock delivery revealed differential degrees of response suppression. Considerably more suppression occurred in the component not associated with the preshock stimulus, thus implicating the discriminative functions of the correlated stimulus.     

Localization of moving sound

The final position of a moving sound source usually appears to be displaced in the direction of motion. We tested the hypothesis that this phenomenon, termed auditory representational momentum, is already emerging during, not merely after, the period of motion. For this purpose, we investigated the localization of a moving sound at different points in time. In a dark anechoic environment, an acoustic target moved along the frontal horizontal plane. In the initial, middle, or final phase of the motion trajectory, subjects received a tactile stimulus and determined the current position of the moving target at the moment of the stimulus by performing either relative-judgment or pointing tasks. Generally, in the initial phase of the auditory motion, the position was perceived to be displaced in the direction of motion, but this forward displacement disappeared in the further course of the motion. When the motion stimulus had ceased, however, its final position was again shifted in the direction of motion. The latter result suggests that representational momentum in spatial hearing is a phenomenon specific to the final point of motion. Mental extrapolation of past trajectory information is discussed as a potential source of this perceptual displacement.     

Localization of moving sound

The final position of a moving sound source usually appears to be displaced in the direction of motion. We tested the hypothesis that this phenomenon, termed auditory representational momentum, is already emerging during, not merely after, the period of motion. For this purpose, we investigated the localization of a moving sound at different points in time. In a dark anechoic environment, an acoustic target moved along the frontal horizontal plane. In the initial, middle, or final phase of the motion trajectory, subjects received a tactile stimulus and determined the current position of the moving target at the moment of the stimulus by performing either relative-judgment or pointing tasks. Generally, in the initial phase of the auditory motion, the position was perceived to be displaced in the direction of motion, but this forward displacement disappeared in the further course of the motion. When the motion stimulus had ceased, however, its final position was again shifted in the direction of motion. The latter result suggests that representational momentum in spatial hearing is a phenomenon specific to the final point of motion. Mental extrapolation of past trajectory information is discussed as a potential source of this perceptual displacement.     

Attentional capture by motion onsets is spatially imprecise

Using straight translatory motion of a visual peripheral cue in the frontoparallel plane, and probing target discrimination at different positions along the cue's motion trajectory, we found that target orientation discrimination was slower for targets presented at or near the position of motion onset (4.2° off centre), relative to the onset of a static cue (Experiment 1), and relative to targets presented further along the motion trajectory (Experiments 1 and 2). Target discrimination was equally fast and accurate in the moving cue conditions relative to static cue conditions at positions further along the cue's motion trajectory (Experiment 1). Moreover, target orientation discrimination was not slowed at the same position, once this position was no longer the motion onset position (Experiment 3), and performance in a target colour-discrimination task was not slowed even at motion onset (Experiment 4). Finally, we found that the onset location of the motion cue was perceived as being shifted in the direction of the cue's motion (Experiment 5). These results indicate that attention cannot be as quickly or precisely shifted to the onset of a motion stimulus as to other positions on a stimulus’ motion trajectory.     

Differential reinstatement predicted by preextinction response rate

Reinstatement refers to the recovery of previously extinguished responding by the responseindependent delivery of a stimulus that was a reinforcer in training. Two experiments were conducted to examine relative reinstatement following the training of differential preextinction response rates, either with equal (Experiment 1) or unequal (Experiment 2) preextinction reinforcement rates. In Experiment 1, each of 3 pigeons first pecked at relatively high rates in the tandem variable-time 117-sec fixed-interval 3-sec component of a multiple schedule and at lower rates in a separate tandem variableinterval 117-sec fixed-time 3-sec component. Reinforcement rates were equal between components. Pecking then was extinguished in each component, before being reinstated under a multiple variabletime 120-sec variable-time 120-sec schedule. Greater reinstatement occurred in the component previously correlated with higher rates of pecking. In Experiment 2, in an initial condition, the mean rate of lever pressing for one group of 8 rats was significantly higher under a fixed-ratio 3 schedule than for another group of 8 rats under a fixed-ratio 1 schedule. Mean reinforcement rate was significantly higher for the group exposed to the fixed-ratio 1 schedule. For each group, lever pressing then was extinguished, before being reinstated under a variable-time 30-sec schedule. Significantly greater mean reinstatement occurred for the group previously exposed to the fixed-ratio 3 schedule. These results suggest that differential reinstatement may be predicted by preextinction response rate, perhaps independently of preextinction reinforcement rate.     

Induced Rotational Motion With Nonabutting Inducing and Induced Stimuli: Implications Regarding Two Forms of Induced Motion

Induced motion is the illusory motion of a static stimulus in the opposite direction to a moving stimulus. Two types of induced motion have been distinguished: (a) when the moving stimulus is distant from the static stimulus and undergoes overall displacement, and (b) when the moving stimulus is pattern viewed within fixed boundaries that abut the static stimulus. Explanations of the 1st type of induced motion refer to mediating phenomena, such as vection, whereas the 2nd type is attributed to local processing by motion-sensitive neurons. The present research was directed to a display that elicited induced rotational motion with the characteristics of both types of induced motion: the moving stimulus lay within fixed boundaries, but the inducing and induced stimuli were distant from each other. The author investigated the properties that distinguished the two types of induced motion. In 3 experiments, induced motion persisted indefinitely, inter-ocular transfer of the aftereffect of induced motion was limited to about 20%, and the time-course of the aftereffect of induced motion could not be attributed to vection. Those results were consistent with fixed-boundary induced motion. However, they could not be explained by local processing. Instead, the results might reflect the detection of object motion within a complex flow-field that resulted from the observer's motion.