[Does auditory information permit the establishment of spatial cues? Experimental and clinical findings in congenital blindness].
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Three experiments were designed to explore parallel and distance alleys as a function of instructions (apparent and objective) under three different distance-cue conditions. The main findings were that (1) the alleys for the apparent instructions were positioned closer to the median plane than those for the objective instructions, (2) in an indoor setting, the parallel and distance alleys were not different under either the apparent or the objective instructions, and (3) in an outdoor setting, the parallel alley lay inside the distance alley under both the apparent and the objective instructions. On the basis of comparison with some of the previous alley studies, it is suggested that exact control of instructions will not produce great discrepancy between the parallel and the distance alleys that were constructed indoors.
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Previous research (e.g., Wong & Weisstein, 1984a, 1985) has shown that flickering stimuli appear to be more distant than nonflickering stimuli at the same physical distance. Given this relation between flicker and perceived depth, inappropriate constancy scaling theories predict that flickering stimuli should be perceived as larger than nonflickering ones. In contrast, links between flicker and motion perception suggest that flickering stimuli should be perceived as smaller than nonflickering ones. Two experiments tested these contrasting predictions. In Experiment 1, 22 subjects compared flickering and nonflickering vertical lines and reported that the flickering stimulus appeared significantly smaller than the nonflickering one. In Experiment 2, 21 subjects reported that the stimuli used in Experiment 1 produced depth effects similar to those reported in previous experiments: flickering stimuli were perceived as more distant than nonflickering ones. The observed effect of flicker on perceived size was contrary to predictions from inappropriate constancy scaling theory, but consistent with views that motion and flicker are processed by the same pathway.
Effective navigation requires knowledge of the direction of motion and of the distance traveled. Humans can use visual motion cues from optic flow to estimate direction of self-motion. Can they also estimate travel distance from visual motion?Optic flow is ambiguous with regard to travel distance. But when the depth structure of the environment is known or can be inferred, i.e., when the flow can be calibrated to the environmental situation, distance estimation may become possible. Previous work had shown that humans can discriminate and reproduce travel distances of two visually simulated self-motions under the assumption that the environmental situation and the depth structure of the scene is the same in both motions. Here we ask which visual cues are used for distance estimation when this assumption is fulfilled. Observers discriminated distances of visually simulated self-motions in four different environments with various depth cues. Discrimination was possible in all cases, even when motion parallax was the only depth cue available. In further experiments we ask whether distance estimation is based directly on image velocity or on an estimate of observer velocity derived from image velocity and the structure of the environment. By varying the simulated height above ground, the visibility range, or the simulated gaze angle we modify visual information about the structure of the environment and alter the image velocity distribution in the optic flow. Discrimination ability remained good. We conclude that the judgment of travel distance is based on an estimate of observer speed within the simulated environment.
Shebilske, Karmiohl, and Proffitt (1983) interpret their data as showing that (a) the reference tonus level of the extraocular muscles controlling vergence is affected by everyday conditions of close viewing, and (b) this naturally induced phoria affects the visual perception of distance under natural viewing conditions. We note that these interpretations do not fully concur with the data presented--for example, the second conclusion favorably conflates partial results from two separate experiments--and we identify a number of confoundings that reduce the likelihood that the reported inaccuracies in distance judgments were due to variations in efference.
Bees returning from a feeder placed in a narrow tunnel that is lined with a chequered pattern will strongly overestimate travel distance. This finding supports the view that their distance estimation is based on integrating optic flow experienced during flight. Here, we use chequered tunnels with various colour combinations as a tool to identify the spectral channel used by bees to gauge travel distance. The probability of bees performing waggle dances after a short travel distance correlates only with the low range of the green contrast of the pattern in the tunnel. But it does not correlate with the pattern's chromatic contrast or brightness contrast. Distance estimation is therefore colour blind. We also evaluated the waggle runs as a function of colour pattern. Their duration is the code for the food source distance. Waggle run duration is entirely independent of the colour pattern used, implying that once green contrast is above detection threshold, distance estimation depends solely on the angular motion of the landscape passed in flight.
When a painting or drawing is viewed monocularly and fixation alternated between points that are at different implied distances from the observer, the covered eye usually makes vergence movements that are directionally appropriate for the indicated depth differences. These vergence changes evoked by perspective artwork vary greatly in magnitude and consistency from one illustration to the next: some drawings and paintings lead to convergence-divergence changes smaller than would be appropriate for the illustrated content, if seen from the implied viewing distance; others are supernormal stimuli, evoking inappropriately large vergence changes in all observers tested.
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The focus of this study was on the ability of infants to perceive whether an object is positioned at a distance that would make contact possible. As a toy was presented, sometimes within and sometimes beyond reach, the initiation of reaching and leaning forward was scored. Infants were divided into leaning and nonleaning groups. Both leaning and nonleaning 5-month-olds changed their behavior dramatically when the object was placed beyond, as opposed to within, reach. The nonleaners showed a decline in reaching when this boundary for contact was crossed. The "leaners" did not; rather, they began to lean forward. These results suggest that 5-month-olds use information for the affordance of contact. 4-month-olds provided less evidence that arm length regulates reaching. 5-month-old infants acted as if they not only had some sensitivity to the absolute distance of an object but also to the effect that leaning forward has on their ability to make contact with a distant object.
Binocular correspondence must be determined if disparity is to be used to provide information about three-dimensional shape. The current study investigated whether knowledge of the statistical distribution of disparities in the natural environment is employed in this process. A simple model, which produces distributions of distances similar to those found in the natural environment, was used to predict the distribution of disparities in natural images. This model predicts that crossed disparities will be more likely as (i) stimulus elevation decreases below fixation and (ii) fixation distance increases. To determine whether these factors influence binocular correspondence for human observers, ambiguous stereograms were presented to observers, as stimulus elevation and fixation distance were manipulated. Clear biases were observed in the depth perceived in these stereograms, which were more likely to be seen as closer than fixation (i) for stimuli presented below fixation and (ii) as fixation distance increased. These results suggest that binocular correspondence is determined in a manner consistent with the distributions of disparities expected in natural scenes.
The distortion of polar perspective depends on the depth of the tridimensional shape and on the observation distance. In four experiments using 54 undergraduates as subjects, we found that a compensation process which takes depth and observation distance into account corrects for such distortions. Compensation was demonstrated in experiments in which deceptive information on depth and on observation distance was provided. The result was distortions of the perceived shapes that would be expected if compensation were based on the deceptive information.
In four experiments, pictures varying in degree of perspective convergence from linear to parallel were observed under the following conditions: at an arbitrary station point, at correct station points, and with unconstrained view. Adults were asked to rank the pictures from the most to least natural and realistic-looking picture or from the most to the least accurate drawing. Subjects nearly always chose the parallel perspective pictures as most preferred and the linear perspective pictures as least preferred. Intermediate degrees of convergence were ranked accordingly. Results were interpreted in light of an argument for a pictorial station poing independent of the correct center of projection for a picture. Since this station point was calculated to be at a distance at least 10 times as great as the object is large, its assumption for pictorial viewing was termed the "Zoom "effect.
Intermittent sounds generated at 270 degrees azimuth and from distances ranging from 2 to 10 feet were recorded on magnetic tape and played back to listeners via headphones. Loudness cues for relative distance were eliminated at the time of recording. Listeners were required to estimate the apparent distance of the recorded sounds when heard monoaurally and binaurally. Most subjects estimated the order of distances correctly. Distance estimations were as proficient when listening monaurally as when listening binaurally. Performance was more accurate for high-pass (greater than 4.0 kHz) noise bursts than for low-pass (less than 1.0 kHz) noise bursts. In a second study, broad-band noise bursts were recorded from azimuthal positions of 360 degrees, 330 degrees, 300 degrees and 270 degrees again at distances ranging from 2 to 10 feet. Estimations of the distances of the sounds, presented via headphones, were most proficient when azimuthal position of the original stimuli was 330 degrees.
The present study aimed to investigate whether the visual system scales apparent depth from binocularly unmatched features by using absolute distance information. In Experiment 1 we examined the effect of convergence on perceived depth in phantom stereograms [Gillam, B., & Nakayama, K. (1999). Quantitative depth for a phantom surface can be based on cyclopean occlusion cues alone. Vision Research, 39, 109-112.], monocular gap stereograms [Pianta, M. J., & Gillam, B. J. (2003a). Monocular gap stereopsis: manipulation of the outer edge disparity and the shape of the gap. Vision Research, 43, 1937-1950.] and random dot stereograms. In Experiments 2 and 3 we examined the effective range of viewing distances for scaling the apparent depths in these stereograms. The results showed that: (a) the magnitudes of perceived depths increased in all stereograms as the estimate of the viewing distance increased while keeping proximal and/or distal sizes of the stimuli constant, and (b) the effective range of viewing distances was significantly shorter in monocular gap stereograms. The first result indicates that the visual system scales apparent depth from unmatched features as well as that from horizontal disparity, while the second suggests that, at far distances, the strength of the depth signal from an unmatched feature in monocular gap stereograms is relatively weaker than that from horizontal disparity.
Experiments on reproducing imposed self-motion showed that not only final distance or angle of motion, but also the temporal profile are reproduced. Reproduction errors have been attributed to sensory inputs, inaccurate memorization of the motion variable, or motor errors. However, another possible source of error has so far been neglected. The internal time base for path integration or movement memorization may be distorted and thus not reflect physical time. Because additional cognitive load was previously shown to affect subjective estimation of duration, we used a dual-task paradigm during either the stimulation or reproduction phase of three different movement reproduction tasks. We asked subjects 1) on a rotating chair to reproduce imposed passive whole body rotations by controlling the chair with a joystick, 2) on a treadmill to actively reproduce locomotion with respect to the treadmill, and 3) while blindfolded to reproduce a previously walked straight trajectory. The cognitive load changed the distance of reproduced self-motion by about 25% depending on whether the mental task was performed while experiencing or reproducing the motion. Although imposed velocity was reproduced accurately in all conditions, reproduced movement duration was affected in the same way as distance. This result implies that for the perception of distance traveled, perceptual space and time are closely interrelated. The findings are consistent with shared processing of temporal and spatial information. A computational model of motion reproduction including a discrete path integrator is proposed that is able to explain the experimental results within one coherent framework.
The present study examined the influence of perceptual organization on the processing of global and local information in hierarchical patterns. In two experiments, we examined whether disturbing the spatial relationships between local elements by introducing between-element distance and size heterogeneity affected global processing dominance. The effects on global processing dominance of undistorted compound stimuli with equidistant and homogeneous local elements were compared with those of compound stimuli which presented between-element distance heterogeneity (Experiment 1) or heterogeneity in size (Experiment 2). The results showed that the global advantage effect decreased similarly under conditions of between-element distance and size heterogeneity that disturbed the spatial relationships between local elements. The results provide new evidence on the role of perceptual organization in hierarchical patterns processing.