Scaling subjective velocity,distance, and duration

By magnitude estimation, the relation between the subjective and physical values of linear velocities, durations, and distances were found to be power functions with exponents of about 0.75, 0.90, and 0.90. When subjective values are substituted for their physical correlates in the equation, velocity = distance/duration, we obtain:

$$subjective velocity = k(\tfrac{{subjective distance}}{{subjective duration}})0.8$$     

On the relation between time and space in the visual discrimination of velocity.

Is the perception of velocity determined by the prior discrimination of spatial and temporal distances? Two experiments sought to answer this question by comparing the discriminabilities of moving stimuli varied in spatial extent, temporal duration, or in redundant combinations of both variables. The subject's task was to identify which of two alternative stimuli was presented on each trial. A set of four stimuli was constructed from two values of spatial extent and two values of temporal duration. Separate conditions required discrimination of each of the six possible pairs of these stimuli. Experiment 1 examined continuous motion and Experiment 2 examined apparent motion for stimuli with short (50 versus 65 msec) and with long (500 versus 650 msec) interstimulus intervals. With continuous motion and with good apparent motion (short intervals), the discrimination between the different-velocity bivariate pairs was too accurate to be attributed only to discriminations of the spatial and temporal extents of the motion. This did not occur with poor apparent motion. Evidently, time and space are perceptually related.     

Depth interval estimates from motion parallax and binocular disparity beyond interaction space

Static and dynamic observers provided binocular and monocular estimates of the depths between real objects lying well beyond interaction space. On each trial, pairs of LEDs were presented inside a dark railway tunnel. The nearest LED was always 40 m from the observer, with the depth separation between LED pairs ranging from 0 up to 248 m. Dynamic binocular viewing was found to produce the greatest (ie most veridical) estimates of depth magnitude, followed next by static binocular viewing, and then by dynamic monocular viewing. (No significant depth was seen with static monocular viewing.) We found evidence that both binocular and monocular dynamic estimates of depth were scaled for the observation distance when the ground plane and walls of the tunnel were visible up to the nearest LED. We conclude that both motion parallax and stereopsis provide useful long-distance depth information and that motion-parallax information can enhance the degree of stereoscopic depth seen.     

Figure and ground in space and time: 2. Frequency, velocity, and perceptual organization

The figure-ground organization of an ambiguous bipartite pattern in which the two regions of the pattern contained sine-wave gratings which differed in spatial frequency was examined for two pairs of spatial frequencies: 1 and 4 cycles deg-1, and 1 and 8 cycles deg-1. The region of higher spatial frequency underwent contrast reversal at one of four rates: 0, 3.75, 7.5, or 15 Hz. The region of lower spatial frequency was equated with either the temporal frequency or the velocity of the grating of higher spatial frequency in three sets of conditions: one stationary condition, three in which temporal frequency was equated, and three in which velocity was equated. For the 1 and 4 cycles deg-1 pair, the region of lower spatial frequency tended to be seen as the background a higher percentage of the time. There were significant linear trends for the appearance as background of the region of lower spatial frequency with respect to the magnitude of the velocity difference between the two regions of the pattern. The faster the 1 cycle deg-1 grating moved with respect to the 4 cycles deg-1 grating, the higher the percentage of the time it was seen as the ground. The results for the 1 and 8 cycles deg-1 pair were in some cases unexpected in that the 8 cycles deg-1 grating was seen as the ground behind the 1 cycle deg-1 grating even though it was of a higher spatial frequency and moved at a slower velocity. The spatiotemporal tuning of the visual system is discussed.     

Seeing and hearing and space and space and time

A previous experiment had shown spatial location to be judged in terms of the framework provided by the modality in which stimuli were presented. In the present study, digits were either auditorally or visually presented, and in either form the three digits appeared successivly to the left, in the center, and to the right of the S. The digit which occurred temporally in the middle of the sequence was never central from the spatial viewpoint. The S was asked to indicate which digit was the middle one. Ss were blind, deaf, or normal. The deaf and two control groups saw visual displays, and the blind and their controls heard auditory displays. The former groups predominantly chose the spatially middle digit and the latter groups the temporally middle. It was concluded that modality of presentation was the trigger which switched in the coding dimension of time or space.     

Dimensional overlap between time and space

Several pieces of evidence suggest that our mental representations of time and space are linked. However, the extent of this linkage between the two domains has not yet been assessed. We present the results of two experiments that draw on the predictions of the dimensional overlap model (Kornblum, Hasbroucq, & Osman, Psychological Review 97:253–270, 1990). The stimulus and response sets in these reaction time experiments were related to either time or space. The obtained stimulus–response congruency effects were of about the same size for identical stimulus–response sets (time–time or space–space) and for different stimulus–response sets (time–space or space–time). These results support the view that our representations of time and space are strongly linked.     

Letters in time and retinotopic space

Various phenomena in tachistoscopic word identification and priming (WRODS and LTRS are confused with and prime WORDS and LETTERS) suggest that position-specific channels are not used in the processing of letters in words. Previous approaches to this issue have sought alternative matching rules because they have assumed that these phenomena reveal which stimuli are good but imperfect matches to a particular word-such imperfect matches being taken by the word recognition system as partial evidence for that word. The new Letters in Time and Retinotopic Space model (LTRS) makes the alternative assumption that these phenomena reveal the rates at which different features of the stimulus are extracted, because the stimulus is ambiguous when some features are missing from the percept. LTRS is successfully applied to tachistoscopic identification and form priming data with manipulations of duration and target-foil and prime-target relationships.     

Perceptual grouping in space and time: Evidence from the Ternus display

We report three experiments investigating the effect of perceptual grouping on the appearance of a bistable apparent-motion (Ternus) display. Subjects viewed a Ternus display embedded in an array of context elements that could potentially group with the Ternus elements. In contrast to several previous findings, we found that grouping influenced apparent motion perception. In Experiment 1, apparent motion perception was significantly affected via grouping by shape similarity, even when the visible persistence of the elements was controlled. In Experiment 2, elements perceived as moving without context were perceived as stationary when grouped with stationary context elements. In Experiment 3, elements perceived as stationary without context were perceived as moving when grouped with moving context elements. We argue that grouping in the spatial and temporal domains interact to yield perceptual experience of apparent-motion displays.     

Top-down control in time and space: Evidence from saccadic latencies and trajectories

Visual distractors disrupt the production of saccadic eye movements temporally, by increasing saccade latency, and spatially, by biasing the trajectory of the movement. The present research investigated the extent to which top-down control can be exerted over these two forms of oculomotor capture. In two experiments, people were instructed to make target directed saccades in the presence of distractors, and temporal and spatial capture were assessed simultaneously by measuring saccade latency and saccade trajectory curvature, respectively. In Experiment 1, an attentional control set manipulation was employed, resulting in the elimination of temporal capture, but only an attenuation of spatial capture. In Experiment 2, foreknowledge of the target location caused an attenuation of temporal capture but an enhancement of spatial capture. These results suggest that, whereas temporal capture is contingent on top-down control, the spatial component of capture is stimulus-driven.     

Across space and time: infants learn from backward and forward visual statistics

This study investigates whether infants are sensitive to backward and forward transitional probabilities within temporal and spatial visual streams. Two groups of 8‐month‐old infants were familiarized with an artificial grammar of shapes, comprising backward and forward base pairs (i.e. two shapes linked by strong backward or forward transitional probability) and part‐pairs (i.e. two shapes with weak transitional probabilities in both directions). One group viewed the continuous visual stream as a temporal sequence, while the other group viewed the same stream as a spatial array. Following familiarization, infants looked longer at test trials containing part‐pairs than base pairs, although they had appeared with equal frequency during familiarization. This pattern of looking time was evident for both forward and backward pairs, in both the temporal and spatial conditions. Further, differences in looking time to part‐pairs that were consistent or inconsistent with the predictive direction of the base pairs (forward or backward) indicated that infants were indeed sensitive to direction when presented with temporal sequences, but not when presented with spatial arrays. These results suggest that visual statistical learning is flexible in infancy and depends on the nature of visual input.     

Saccades compress space, time and number

It has been suggested that space, time and number are represented on a common subjective scale. Saccadic eye movements provide a fascinating test. Saccades compress the perceived magnitude of spatial separations and temporal intervals to approximately half of their true value. The question arises as to whether saccades also compress number. They do, and compression follows a very similar time course for all three attributes: it is maximal at saccadic onset and decreases to veridicality within a window of approximately 50ms. These results reinforce the suggestion of a common perceptual metric, which is probably mediated by the intraparietal cortex; they further suggest that before each saccade the common metric for all three is reset, possibly to pave the way for a fresh analysis of the post-saccadic situation.     

Indexing space and time in film understanding

We investigated the extent to which understanders monitor shifts in time and space during film comprehension. Participants viewed a feature‐length film and identified those points in the film in which they perceived a change in situation. We performed an a priori analysis of the films to identify the shifts in time, the movement of characters, and region. The relationship between the theoretical analysis of the films and the participants judgements of situational change was assessed. The results provide support for the Event Indexing Model and suggest that situation models for filmed events are indexed along multiple dimensions of situational continuity. Furthermore, the pattern of results was similar for narrative film as they are for narrative text. This finding suggest that there are general mechanisms for event understanding that operate independently of medium or mode of experience. Copyright © 2001 John Wiley & Sons, Ltd.     

Tracking visual search over space and time

Visual perception consists of early preattentive processing and subsequent attention-demanding processing. Most researchers implicitly treat preattentive processing as a domain-dependent, indivisible stage. We show, however, by interrupting preattentive visual processing of color before its completion, that it can be dissected both temporally and spatially. The experiment depends on changing easy (preattentive) selection into difficult (attention-demanding) selection. We show that although the mechanism subserving preattentive selection completes processing as early as 200 msec after stimulus onset, partial selection information is available well before completion. Furthermore, partial selection occurs first at locations near fixation, spreading radially outward as processing proceeds.     

Fingerstroke time estimates for touchscreen-based mobile gaming interaction

The growing popularity of gaming applications and ever-faster mobile carrier networks have called attention to an intriguing issue that is closely related to command input performance. A challenging mirroring game service, which simultaneously provides game service to both PC and mobile phone users, allows them to play games against each other with very different control interfaces. Thus, for efficient mobile game design, it is essential to apply a new predictive model for measuring how potential touch input compares to the PC interfaces. The present study empirically tests the keystroke-level model (KLM) for predicting the time performance of basic interaction controls on the touch-sensitive smartphone interface (i.e., tapping, pointing, dragging, and flicking). A modified KLM, tentatively called the fingerstroke-level model (FLM), is proposed using time estimates on regression models.