Reversals of visual depth caused by motion parallax

The role of the velocity and direction of retinal movement in the determination of apparent depth from motion parallax was examined. Motion parallax was produced either by linking the movement of random-dots to head movement or by making this motion independent of the head movement. The results show that apparent depth was largely estimated from the velocity difference between the stimuli. The direction of retinal movement in the absence of head movement did not determine whether the pattern appeared to protrude or recede. Information about direction linked to head movement was able to stabilize protrusion/recession by providing a cue for the location of the fixation point. Depth reversal occurred less frequently in the presence than in the absence of head movement. When the fixation point shifted from the apparently protruding pattern to the apparently receding pattern, in both the presence and absence of head movement, depth reversal was readily observed.     

Independence of sampling of motion parallax and binocular disparity in discrimination of depth1

Abstract: The sampling strategy of the visual system in binocular disparity and motion parallax to discriminate depth was investigated. Human observers were asked to discriminate between the depths of two surfaces defined by both cues. Gaussian noise was added to the depths represented by each cue, and the correlation in noise was manipulated. Human performance was compared with two types of likelihood models. The first was based on independent sampling, in which data from the two cues were gathered from independent sets of points in the display. The second was based on paired sampling, in which data from these cues were gathered from the same set of points. The former model yielded a better fit with human performance. This suggests that the visual system is more likely to adopt independent sampling.     

Dynamic occlusion and motion parallax in depth perception

Random-dot techniques were used to examine the interactions between the depth cues of dynamic occlusion and motion parallax in the perception of three-dimensional (3-D) structures, in two different situations: (a) when an observer moved laterally with respect to a rigid 3-D structure, and (b) when surfaces at different distances moved with respect to a stationary observer. In condition (a), the extent of accretion/deletion (dynamic occlusion) and the amount of relative motion (motion parallax) were both linked to the motion of the observer. When the two cues specified opposite, and therefore contradictory, depth orders, the perceived order in depth of the simulated surfaces was dependent on the magnitude of the depth separation. For small depth separations, motion parallax determined the perceived order, whereas for large separations it was determined by dynamic occlusion. In condition (b), where the motion parallax cues for depth order were inherently ambiguous, depth order was determined principally by the unambiguous occlusion information.     

Motion parallax driven by head movements: conditions for visual stability, perceived depth, and perceived concomitant motion

Yoking the movement of the stimulus on the screen to the movement of the head, we examined visual stability and depth perception as a function of head-movement velocity and parallax. In experiment 1, for different head velocities, observers adjusted the parallax to find (a) the depth threshold and (b) the concomitant-motion threshold. Between these thresholds, depth was seen with no perceived motion. In experiment 2, for different head velocities, observers adjusted the parallax to produce the same perceived depth. A slower head movement required a greater parallax to produce the same perceived depth as faster head movements. In experiment 3, observers reported the perceived depth for different parallax magnitudes. Perceived depth covaried with smaller parallax without motion perception, but began to decrease with larger parallax and concomitant motion was seen. Only motion was seen with the larger parallax.     

Development of depth perception mediated by motion parallax in unidimensional projections of rotation in depth.

Motion parallax is a composite of five transformations demonstrated to be effective in adult judgments of rotation direction in polar motion projections of a horizontal row of dots rotating in depth. The effectiveness of these transformations as a function of age was tested by presenting six such motion projections to first graders (age = 6 years), seventh graders (age = 13 years), and college students (age = 19 years). Identical age functions were obtained for judged rotation direction from the four motion projections representing (1) Velocity, corresponding to the traditional definition of motion parallax as differential velocity, (2) Velocity plus differences between ratios of instantaneous displacement to instantaneous acceleration for dots on the near and far sides of the rotation axis ($\text{D}\text{A}$ Difference), (3) Velocity, $\text{D}\text{A}$ Difference, and a gradient across the row of $\text{D}\text{A}$ ratios, and (4) all transformations. First graders, unable to use horizontal transformations, performed at chance on these four projections, while older students made correct judgments. Order, separated from Velocity for the first time, resulted in chance performance at all ages, while Direction, also separated from Velocity for the first time, resulted in veridical judgments in only 4 of 24 college students.     

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.     

Detectability of motion as a factor in depth perception by monocular movement parallax

A display of two objects at different distances was presented to 10 observers, who were requested in two experiments to match the width of the more distant (comparison) object to the width of the nearer (standard) one under conditions permitting monocular observation and lateral head motion. The matched width of the comparison object was considered a measure of the effectiveness of movement parallax. The effectiveness of movement parallax decreases with increasing angular separation of the objects and with increasing background distance. A background without visible texture leads to a better perception of depth between two objects than a textured background The results can be explained by postulating that, whenever the detectability of motion is enhanced, i.e., the threshold for the detection of motion is lowered, the effectiveness of movement parallax as a cue to depth is increased.     

Temperature reinforcement for visual discrimination training in baby chicks

A fully automated training apparatus, using thermoregulation as performance incentive, was constructed to train baby chicks on visual discrimination and reversal problems. In the base condition, the S is bathed in cold air in a small training cubicle. Two stimuli are back-projected onto two display windows according to a pseudorandom balanced schedule. A peck at the positive stimulus gives convective as well as radiant heat reward with adjustable temperature and duration. A peck at the negative stimulus merely advances the program to the next trial. Permanent printout records give trial-to-trial information on response choice and latency. Performance data of 64 Ss are reported.     

Disruption of eye movements by ethanol intoxication affects perception of depth from motion parallax

Motion parallax, the ability to recover depth from retinal motion generated by observer translation, is important for visual depth perception. Recent work indicates that the perception of depth from motion parallax relies on the slow eye movement system. It is well known that ethanol intoxication reduces the gain of this system, and this produces the horizontal gaze nystagmus that law enforcement's field sobriety test is intended to reveal. The current study demonstrates that because of its influence on the slow eye movement system, ethanol intoxication impairs the perception of depth from motion parallax. Thresholds in a motion parallax task were significantly increased by acute ethanol intoxication, whereas thresholds for an identical test relying on binocular disparity were unaffected. Perhaps a failure of motion parallax plays a role in alcohol-related driving accidents; because of the effects of alcohol on eye movements, intoxicated drivers may have inaccurate or inadequate information for judging the relative depth of obstacles from motion parallax.     

Form preferences in successive discrimination learning of young chicks.

In four experiments the effects of form and orientation pecking preferences of 1- and 3-day old Vantress X Arbor Acre chicks on successive discrimination learning were determined, using heat reinforcement. Major findings were as follows: (a) The young chick has both circle and verticle orientation pecking preferences that are present during at least the first 3 days after hatching; (b) when either of these preferred cues is the nonreinforced cue, the young chick has difficulty in learning not to respond to it but learns quickly not to respond to an unpreferred cue (e.g., triangle and horizontal oriented dots or bar); and (c) these pecking preferences can be modified by heat reinforcement, and the effects of this conditioning is evidenct in subsequent extinction and retention tests. The main conclusion from these experiments is that form and orientation preferences, like brightness and color preferences, are important developmental constraints on conditioning of the young chick.     

Aging and the perception of depth and 3-D shape from motion parallax

The ability of younger and older observers to perceive 3-D shape and depth from motion parallax was investigated. In Experiment 1, the observers discriminated among differently curved 3-dimensional (3-D) surfaces in the presence of noise. In Experiment 2, the surfaces' shape was held constant and the amount of front-to-back depth was varied; the observers estimated the amount of depth they perceived. The effects of age were strongly task dependent. The younger observers' performance in Experiment 1 was almost 60% higher than that of the older observers. In contrast, no age effect was obtained in Experiment 2. Older observers can effectively perceive variations in depth from patterns of motion parallax, but their ability to discriminate 3-D shape is significantly compromised.     

The roles of convergence and apparent distance in depth constancy with motion parallax

The question of whether motion parallax is calibrated by convergence or by apparent distance for depth perception was addressed in three experiments. In Experiment 1, a random dot parallactic display was viewed monocularly at a distance of 80 cm, and the convergence angles were set for distances of 40, 60, and 80 cm. Averaged apparent depth was not different across conditions. In Experiment 2, a display consisting of one surface showing dollar bills and one surface showing random dots was viewed monocularly at a distance of 80 cm. It was presented at two different apparent distances, which were manipulated by varying the size of the dollar bills. In one condition, normally sized dollar bills were presented, and in another condition, the size was reduced by 30%. The averaged apparent depth associated with the small-bill display was larger than the depth associated with the normally sized bill display. In Experiment 3, a random dot display was viewed monocularly at 120 cm. In the primary condition, the random dot display was viewed with an induction screen at 80 cm, and it was moved from side to side such that it appeared stationary and close to the plane of the induction screen. In a comparison condition, the display was viewed without the induction screen and was moving from side to side at 120 cm. In another comparison condition, the display was again viewed without the induction screen but was stationary at 120 cm. Observers adjusted the extent of motion parallax so that apparent depth was 1 cm. The mean extent of parallax was larger in the primary conditio.(ABSTRACT TRUNCATED AT 250 WORDS)     

The visual control of reaching and grasping: binocular disparity and motion parallax

The primary visual sources of depth and size information are binocular cues and motion parallax. Here, the authors determine the efficacy of these cues to control prehension by presenting them in isolation from other visual cues. When only binocular cues were available, reaches showed normal scaling of the transport and grasp components with object distance and size. However, when only motion parallax was available, only the transport component scaled reliably. No additional increase in scaling was found when both cues were available simultaneously. Therefore, although equivalent information is available from binocular and motion parallax information, the latter may be of relatively limited use for the control of the grasp. Binocular disparity appears selectively important for the control of the grasp.     

Nimodipine alters acquisition of a visual discrimination task in chicks

Chicks 5 days old received intraperitoneal injections of nimodipine 30 min before training on either a visual discrimination task (0, 0.5, 1.0, or 5.0 mg/kg) or a test of separation-induced distress vocalizations (0, 0.5, or 2.5 mg/kg). Chicks receiving 1.0 mg/kg nimodipine made significantly fewer visual discrimination errors than vehicle controls by trials 41-60, but did not differ from controls 24 h later. Chicks in the 5 mg/kg group made significantly more errors when compared to controls both during acquisition of the task and during retention. Nimodipine did not alter separation-induced distress vocalizations at any of the doses tested, suggesting that nimodipine's effects on learning cannot be attributed to a reduction in separation distress. These data indicate that nimodipine's facilitation of learning in young subjects is dose dependent, but nimodipine failed to enhance retention.     

Effects of static and motion parallax depth information on perception of size in children and adults

The effects of static and kinetic information for depth on judgments of the relative size of objects placed at different distances was studied in 3- and 7-yr-old children and adults. Subjects viewed either a pair of objects placed on the floor of a textured alley or a projected slide of the identical scene. The presence of motion parallax information for depth was also manipulated. All subjects showed a clear sensitivity to static pictorial depth information in judging objects placed so they projected equal retinal areas. When the retinal size of objects was very different, however, children tended to respond to retinal rather than physical size. Motion parallax information increased responsiveness to depth when a 3-dimensional scene was being viewed, but decreased responsiveness with 2-dimensional projections. The decrease was greater in children than adults.