The interaction of perceived distance with the perceived direction of visual motion during movements of the eyes and the head

A horizontally moving target was followed by rotation of the eyes alone or by a lateral movement of the head. These movements resulted in the retinal displacement of a vertically moving target from its perceived path, the amplitude of which was determined by the phase and amplitude of the object motion and of the eye or head movements. In two experiments, we tested the prediction from our model of spatial motion (Swanston, Wade, & Day, 1987) that perceived distance interacts with compensation for head movements, but not with compensation-for eye movements with respect to a stationary head. In both experiments, when the vertically moving target was seen at a distance different from its physical distance, its perceived path was displaced relative to that seen when there was no error in pereived distance, or when it was pursued by eye movements alone. In a third experiment, simultaneous measurements of eye and head position during lateral head movements showed that errors in fixation were not sufficient to require modification of the retinal paths determined by the geometry of the observation conditions in Experiments 1 and 2.     

The interaction of perceived distance with the perceived direction of visual motion during movements of the eyes and the head.

A horizontally moving target was followed by rotation of the eyes alone or by a lateral movement of the head. These movements resulted in the retinal displacement of a vertically moving target from its perceived path, the amplitude of which was determined by the phase and amplitude of the object motion and of the eye or head movements. In two experiments, we tested the prediction from our model of spatial motion (Swanston, Wade, & Day, 1987) that perceived distance interacts with compensation for head movements, but not with compensation for eye movements with respect to a stationary head. In both experiments, when the vertically moving target was seen at a distance different from its physical distance, its perceived path was displaced relative to that seen when there was no error in perceived distance, or when it was pursued by eye movements alone. In a third experiment, simultaneous measurements of eye and head position during lateral head movements showed that errors in fixation were not sufficient to require modification of the retinal paths determined by the geometry of the observation conditions in Experiments 1 and 2.     

More things in heaven and earth than are dreamt of in the initial letter acuity hypothesis

Schwartz, Montagner, and Kirsner (1987 Brain and Language, 31, 301-307) claim that length X visual hemifield interactions for recognition of horizontal words reflect acuity differences for the initial letters of short and long words rather than different methods of lexical access for words presented in the LVF and in the RVF. They argue that Young and Ellis did not satisfactorily eliminate this possibility because they (Young & Ellis, 1985, Brain and Language, 24, 326-358, Experiment 3) allowed the use of sophisticated guessing strategies. We demonstrate that the presentation conditions of the Schwartz et al. (1987) experiment are different from those of our (Young & Ellis, 1985) experiments in potentially important ways, and that the acuity gradient explanation proposed by Schwartz et al. to account for word length X visual hemifield interactions is inadequate in terms of both the existing literature and a reanalysis of data from our own (Young & Ellis, 1985) Experiments 1 and 3.     

To cross or not to cross: Impact of visual and auditory cues on pedestrians’ crossing decision-making

The controlled study of pedestrians’ crossing decision-making is relevant to the search for better safety conditions for this class of vulnerable road users. Several risk factors have been identified in the literature related to the crosswalks’ surrounding environment, the socio-demographic characteristics of the pedestrians crossing the road and the place where the crosswalks are inserted, as well as situational variables, such as speed and distance of the approaching vehicle during the crossing. In this work, the roles of visual and auditory cues in crossing decisions were analysed, comparing different speeds and distances, and taking into consideration different speed patterns of the approaching vehicle, aiming to identify what can affect pedestrians’ crossing behaviour. Experiments were performed in a virtual environment. Participants were presented with 10 different stimuli featuring a vehicle approaching with different speeds and movement patterns, combined with 2 auditory conditions: one concerning a vehicle with a gasoline combustion engine and another one with no sound cues. Participants were tasked with indicating the moment they decided to cross the street when they thought it was safe to do so by pressing a response button. Percentage of crossings, response time (RT), and time-to-passage (TTP) were recorded and subsequently analysed. The results showed that lower speeds and higher distances lead to higher percentages of crossings and RTs. The auditory condition did not significantly affect participants’ responses, leading to the conclusion that participants’ crossing decision was especially based on their visual perception of the movement characteristics of the approaching vehicle, particularly its speed and distance. These results may have relevance for the development of communication strategies between the vehicles, especially the automated ones, and pedestrians.     

Distorted distance estimation induced by a self-relevant national boundary

Six experiments explored the possibility that the categorization of self versus not-self can distort visual estimations of distance. In Experiments 1-3, Americans overestimated the distance between a U.S. location and a foreign location relative to a visually equidistant U.S. location. In Experiment 4, Canadians overestimated foreign relative to Canadian locations. Experiment 5 showed that this effect occurs even when the domestic context is not physically contiguous. Experiment 6 showed that distance distortion occurs only when crossing one’s own border to a foreign location, not when crossing borders from one foreign location to another. Thus, crossing the psychological boundary between self and not-self creates a visual illusion that distorts on-line distance estimates.     

The spatial distribution of attention following an exogenous cue

Three target-discrimination experiments were conducted to explore the spatial distribution t)f covert visual attention following an exogenous cue. On each trial, a brief peripheral onset was followed by a target stimulus in an otherwise empty visual field at one of eight (Experiment 1) or one of four (Experiments 2 and 3) possible locations centered at the fixation point. The spatial relation between the cue and the target was manipulated. The main results were that (1) performance was better at the cued location than at another nearby location in the same visual quadrant; (2) performance was not affected by the major horizontal and vertical visual meridians; and (3) performance was affected by the spatial distance between the cued and target locations. Together, the results suggest that the spatial distribution of exogenously oriented attention cart be most easily integrated with a simple gradient model.     

Auditory and audiovisual inhibition of return

Two experiments examined any inhibition-of-return (IOR) effects from auditory cues and from preceding auditory targets upon reaction times (RTs) for detecting subsequent auditory targets. Auditory RT was delayed if the preceding auditory cue was on the same side as the target, but was unaffected by the location of the auditorytarget from the preceding trial, suggesting that response inhibition for the cue may have produced its effects. By contrast, visual detection RT was inhibited by the ipsilateral presentation of a visual target on the preceding trial. In a third experiment, targets could be unpredictably auditory or visual, and no peripheral cues intervened. Both auditory and visual detection RTs were now delayed following an ipsilateral versus contralateral target in either modality on the preceding trial, even when eye position was monitored to ensure central fixation throughout. These data suggest that auditory target—target IOR arises only when target modality is unpredictable. They also provide the first unequivocal evidence for cross-modal IOR, since, unlike other recent studies (e.g., Reuter-Lorenz, Jha, & Rosenquist, 1996; Tassinari & Berlucchi, 1995; Tassinari & Campara, 1996), the present cross-modal effects cannot be explained in terms of response inhibition for the cue. The results are discussed in relation to neurophysiological studies and audiovisual links in saccade programming.     

Illegal crossing behavior of pedestrians at signalized intersections: Factors affecting the gap acceptance

Purpose of designing crosswalks is to allow pedestrians to cross the roads safely avoiding conflicts between pedestrians and motorized vehicles. However, pedestrians do not always comply with the crossing rules, whether it is timing (signalization) and/or location (crossing facility). An observation survey of illegal crossings was conducted at six intersections in Izmir, Turkey to determine the distance and time gap perception of the pedestrians for safe road-crossing within the 25 m of the crosswalk. Each intersection was observed on weekdays during afternoon (12.30–13.30) and evening peak hours (17.00–18.00). Totally, 444 illegal crossings were observed at all intersections. Data were analyzed playing the video recordings in office. All roads were consisted of two lanes. In this study pedestrians’ illegal crossing behavior at signalized intersections depending on the position of the oncoming vehicle is of interest. Safety margins and crossing times of the pedestrians were also reported. Position of the vehicle was determined for the first lane at the instant the pedestrian stepped the lane. Pedestrians’ distance gap perception was categorized into five groups depending on the position of the oncoming vehicle which are; vehicle is within the 25 m of the crosswalk, vehicle is within the 25–50 m of the crosswalk, vehicle is within the 50–75 m of the crosswalk, vehicle is just beyond 75 m, and vehicle is out of field of view. Factors affecting the distance gaps, safety margins and crossing times were analyzed by ANOVA. The most significant effect was the vehicle speed in all analysis. Pedestrians based their decision of crossing on distance rather than time gap.     

Response Timing Accuracy as a Function of Movement Velocity and Distance

In two experiments, patterns of response error during a timing accuracy task were investigated. In Experiment 1. these patterns were examined across a full range of movement velocities, which provided a test of the hypothesis that as movement velocity increases, constant error (CE) shifts from a negative to a positive response bias, with the zero CE point occurring at approximately 50% of maximum movement velocity (Hancock & Newell, 1985). Additionally, by examining variable error (VE), timing error variability patterns over a full range of movement velocities were established. Subjects (N = 6) performed a series of forearm flexion movements requiring 19 different movement velocities. Results corroborated previous observations that variability of timing error primarily decreased as movement velocity increased from 6 to 42% of maximum velocity. Additionally, CE data across the velocity spectrum did not support the proposed timing error function. In Experiment 2, the effect(s) of responding at 3 movement distances with 6 movement velocities on response timing error were investigated. VE was significantly lower for the 3 high-velocity movements than for the 3 low-velocity movements. Additionally, when MT was mathematically factored out. VE was less at the long movement distance than at the short distance. As in Experiment 1, CE was unaffected by distance or velocity effects and the predicted CE timing error function was not evident.     

Confusability and interference between members of parafoveal letter pairs

In each of three experiments, confusability between members of a parafoveally exposed pair of letters affected accuracy of identifying the peripheral, but not the central, letter. Confusability was determined from a confusion matrix developed for each subject. In Experiment 1, only one letter in each pair was identified on each exposure, and the position of pair members was varied over trials while the absolute position of the pair was held at a constant distance from fixation. In Experiment 2, both letters were identified on each exposure. In Experiment 3, the criterion letter was presented at a constant distance from fixation, and both letters were identified on each exposure. Since results in Experiment 3 were the same as in Experiments 1 and 2, the effect cannot be explained with reference to an interaction between confusability and acuity. The implications of the findings for various models of visual information processing are discussed.     

Response Timing Accuracy as a Function of Movement Velocity and Distance

In two experiments, patterns of response error during a timing accuracy task were investigated. In Experiment 1, these patterns were examined across a full range of movement velocities, which provided a test of the hypothesis that as movement velocity increases, constant error (CE) shifts from a negative to a positive response bias, with the zero CE point occurring at approximately 50% of maximum movement velocity (Hancock & Newell, 1985). Additionally, by examining variable error (VE), timing error variability patterns over a full range of movement velocities were established. Subjects (N = 6) performed a series of forearm flexion movements requiring 19 different movement velocities. Results corroborated previous observations that variability of timing error primarily decreased as movement velocity increased from 6 to 42% of maximum velocity. Additionally, CE data across the velocity spectrum did not support the proposed timing error function. In Experiment 2, the effect(s) of responding at 3 movement distances with 6 movement velocities on response timing error were investigated. VE was significantly lower for the 3 high-velocity movements than for the 3 low-velocity movements. Additionally, when MT was mathematically factored out, VE was less at the long movement distance than at the short distance. As in Experiment 1, CE was unaffected by distance or velocity effects and the predicted CE timing error function was not evident.     

New equally readable charts based on anisotropy of peripheral visual acuity1

Abstract: Anstis’ equally readable chart for visual acuity has been widely quoted in textbooks on visual perception. However, this chart does not reflect the anisotropy of peripheral visual acuity that has been reported by previous studies. Here, the authors reexamined peripheral visual acuity by measuring resolution thresholds for Landolt rings and recognition thresholds for hiragana letters as a function of retinal eccentricity across two principal retinal meridians: horizontal and vertical. Observers were required to identify the orientation of a gap in the Landolt ring or recognize a hiragana letter while the stimulus was moved slowly from the periphery toward the fovea across each of four meridians: nasal, temporal, superior, and inferior. The results revealed the horizontal‐vertical anisotropy of visual acuity in accordance with the results of previous studies. The mean thresholds obtained in the vertical meridian were approximately 1.51‐fold (for Landolt rings) and 1.42‐fold (for hiragana letters) higher than those obtained in the horizontal meridian at the same retinal eccentricity. The authors propose new equally readable charts for Landolt rings and hiragana letters.     

Motor Programming as a Function of Constraints on Movement Initiation

Three experiments are reported that test the hypothesis that under certain conditions programming time is a function of the directional accuracy demand of a response, directional accuracy being quantified by the minimal angle subtended at the point of movement initiation by the circular targets within the response. Subjects in three simple reaction time experiments were required to tap a single target or a series of circular targets as rapidly as possible with a hand-held stylus. Experiments 1 and 3 showed that the subtended angle (SA) of a response can have a more powerful effect on programming time, as indexed by reaction time and premotor time, than the number of movement parts in the response. The results of Experiment 2 revealed that the locus of the directional accuracy effect was SA and not target size or movement distance. In all three experiments, response SA was a better predictor of programming time than was number of movement parts, target size, movement distance, movement time, and average movement velocity. The findings support the notion that constraints placed upon movement initiation by the directional accuracy demand of the task can play an important role in determining the length of the programming process.     

Motor programming as a function of constraints on movement initiation

Three experiments are reported that test the hypothesis that under certain conditions programming time is a function of the directional accuracy demand of a response, directional accuracy being quantified by the minimal angle subtended at the point of movement initiation by the circular targets within the response. Subjects in three simple reaction time experiments were required to tap a single target or a series of circular targets as rapidly as possible with a hand-held stylus. Experiments 1 and 3 showed that the subtended angle (SA) of a response can have a more powerful effect on programming time, as indexed by reaction time and premotor time, than the number of movement parts in the response. The results of Experiment 2 revealed that the locus of the directional accuracy effect was SA and not target size or movement distance. In all three experiments, response SA was a better predictor of programming time than was number of movement parts, target size, movement distance, movement time, and average movement velocity. The findings support the notion that constraints placed upon movement initiation by the directional accuracy demand of the task can play an important role in determining the length of the programming process.     

Differential effects of cue changes and task changes on task-set selection costs

A task-switching paradigm with a 2:1 mapping between cues and tasks was used to separate cue-switching processes (indexed through pure cue-switch costs) from actual task-switching processes (indexed through additional costs in case of cue and task changes). A large portion of total switch costs was due to cue changes (Experiments 1 and 2), and cue-switch costs but not task-switch costs were sensitive to effects of practice (Experiment 1) and preparation (Experiment 2). In contrast, task-switch costs were particularly sensitive to response-priming effects (Experiments 1 and 2) and task-set inhibition (Experiment 3). Results suggest two processing stages relevant during task-set selection: cue-driven retrieval of task rules from long-term memory and the automatic application of rules to a particular stimulus situation.     

The costs of changing the representation of action: response repetition and response-response compatibility in dual tasks

In 5 experiments, the authors investigated the costs associated with repeating the same or a similar response in a dual-task setting. Using a psychological refractory period paradigm, they obtained response-repetition costs when the cognitive representation of a specific response (i.e., the category-response mapping) changed (Experiment 1) but benefits when it did not change (Experiment 2). The analogous pattern of results was found for conceptually similar (i.e. compatible) responses. Response-response compatibility costs occurred when the cognitive representations of the compatible responses were different (Experiments 3A & 3B), but compatibility benefits occurred when they were the same (Experiment 4). The authors interpret the costs of repeating an identical or compatible response in terms of a general mechanism of action selection that involves coding the task-specific meaning of a response.     

Fitts’ Law is modulated by movement history

Fitts’ Law is one of the most robust and well-studied principles in psychology. It holds that movement time (MT) for target-directed aiming movements increases as a function of target distance and decreases as a function of target width. The purpose of this study was to determine whether Fitts’ Law is affected not only by the demands of the target on the current trial but also by the requirements for performance on the previous trial. Experiments 1 and 2 examined trial-to-trial effects of varying target width; Experiment 3 examined trial-to-trial effects of varying target distance. The findings from Experiments 1 and 2 showed that moving a finger or cursor towards a large object on a previous trial shortened the movement time on the current trial, whereas the opposite occurred with a small object. In contrast, target distance on the previous trial had no effect on movement time on the current trial. These findings suggest that performance on trial n has a clear and predictable effect on trial n+1 (at least for target width) and that Fitts’ Law as it is normally expressed does not accurately predict performance when the width of the target varies from trial to trial.     

Cognitive Strategies and Short-term Memory for Movement Distance and Location

A number of researchers (e.g. Kerr, 1978; Walsh, Russell, Imanaka, & James, 1979) have previously demonstrated interference between location and distance information in motor short-term memory. This interference manifests itself in a characteristic pattern of undershooting and overshooting, with reproduction movement location being drawn in the direction of criterion movement distance and, conversely, the distance of reproduction movements being influenced by the terminal location of the criterion movement. We investigated the effects of different cognitive strategies upon the appearance of this location-distance interference during the reproduction of movement location (Experiment 1) and distance (Experiments 2 and 3) in a linear arm positioning task. Experiment 1 compared performance in location reproduction between two strategy groups differing in the availability of explicit information about the change in starting position. The characteristic undershooting-overshooting interference pattern was observed for the group without the explicit information about the change in starting position but disappeared for the group in which explicit information about the change in starting position was provided. Experiment 2 examined the systematic undershooting-overshooting pattern in distance reproduction for a location strategy (involving some extrapolation of the start and end locations), a counting strategy, and a distance sense strategy (involving the use of visual imagery). The systematic response bias pattern disappeared when the subjects used a location strategy but was clearly observed for the subjects using the other two strategies. This finding was generally confirmed by Experiment 3, which showed a typical undershooting-overshooting pattern in distance reproduction for a counting/distance sense strategy but not for two location strategies (a general location and an explicit location strategy). The location strategies differed in the availability of explicit information about starting and end locations for both the criterion and reproduction movements. The results from these three experiments indicate that explicit information about the start andlor end locations prevents the usual interference between location and distance information from arising in movement reproduction. The notions of automatic and controlled processing and cerebral hemispheric specialization are discussed as potential explanations of these results and of the interference typically observed in motor short-term memory between distance and location information.     

Local processes in preattentive feature detection.

Sagi and Julesz (1987) claimed that for a target to be detected preattentively, it must be within some small critical distance of a nontarget. The independent effects of separation and display size, which were confounded in the Sagi and Julesz experiments, were examined. Experiments 1 and 2 revealed that in tasks requiring search for a color-defined target, target-nontarget separation had no effect on reaction time (RT). Display size, however, was inversely related to RT. Experiment 3 ruled out the possibility that the decreasing function of RT with display size was due to arousal caused by higher display luminance. When nontarget grouping was inhibited, (Exp. 4) it was found that RT no longer decreased with increasing display size. This suggests that nontarget grouping may have been the cause of the improved performance at larger display sizes. Experiments 5 and 6 extended the results to line segments, the stimuli used by Sagi and Julesz.     

Repetition blindness and illusory conjunctions: errors in binding visual types with visual tokens.

Repetition blindness (Kanwisher, 1986, 1987) has been defined as the failure to detect or recall repetitions of words presented in rapid serial visual presentation (RSVP). The experiments presented here suggest that repetition blindness (RB) is a more general visual phenomenon, and examine its relationship to feature integration theory (Treisman & Gelade, 1980). Experiment 1 shows RB for letters distributed through space, time, or both. Experiment 2 demonstrates RB for repeated colors in RSVP lists. In Experiments 3 and 4, RB was found for repeated letters and colors in spatial arrays. Experiment 5 provides evidence that the mental representations of discrete objects (called "visual tokens" here) that are necessary to detect visual repetitions (Kanwisher, 1987) are the same as the "object files" (Kahneman & Treisman, 1984) in which visual features are conjoined. In Experiment 6, repetition blindness for the second occurrence of a repeated letter resulted only when the first occurrence was attended to. The overall results suggest that a general dissociation between types and tokens in visual information processing can account for both repetition blindness and illusory conjunctions.