Dichoptic induction of movement aftereffects contingent on color and on orientation

Some comparative experiments on the dichoptic induction of the movement aftereffect (MAE) contingent on color and the MAE contingent on orientation are reported. Colorcontingent movement aftereffects could be evoked only when the eye which had viewed color during adaptation also viewed color during test sessions. When the apparent color of the test field was changed by binocular color rivalry, contingent movement aftereffects (CMAEs) appropriate to the suppressed color were reported. After dichoptic induction of the orientation-contingent MAE, aftereffects could be obtained whether the eliciting gratings and stationary test fields were presented together to either eye alone or were dichoptically viewed.     

Contingent aftereffects: lateral interactions between color and motion

A randomly dotted yellow disk was rotated at a speed of 5 rpm, alternating in direction every 10 sec. Its change in direction of rotation was paired with a change in surround color, which was either red or green. After 15 min of exposure, observers reported vivid motion aftereffects contingent on the color of both the stationary disk and the surround, even though during adaptation only motion or color was associated with either alone. In further experiments, it was established that a change in color (or direction of motion) of the disk could be associated with a change in direction of motion (or color) of the surround. Such lateral effects were found even when a wide (5 degree) annulus was introduced between the disk and the surround during adaptation and testing. Furthermore, the aftereffects generalized to the annulus, which was not associated with either color or motion during adaptation. However, when the disk alone was adapted to color and motion, no generalization to the surround was found (and vice versa), suggesting that the effects are not produced by adaptation of large receptive fields or by scatter of light within the eye. The results appear to conflict with the ideas that contingent aftereffects are confined to the adapted area of the retina and that they are built up by links between single-duty neurones, and with an extreme view of the segregation of color and motion early in human vision.     

The relation between category and magnitude estimates of tactile intensity

The effect of various types (sandpaper, spoke, spiral, and white) and speeds (0, 1/2, 3, 6, 12, and 30 rpm) of rotating disk backgrounds upon 276 Ss’ estimates of the apparent verticality of a line moved toward physical verticality in either a clockwise or counterclockwise direction was investigated. The general finding was that the estimate of verticality was displaced away from pretest judgments in the direction of the disk rotation. The speed of rotation was significant with maximal vertical displacement at 6 rpm. The direction of line movement was significant with the result that maximal vertical displacement occurred when the line was moved in opposition to the direction of disk rotation. The type of disk employed made a significant difference in the estimates only when the line movement was opposite from the direction of disk rotation. Disks with inadequate stimulus contours (white) produced no significant effect. Results are discussed in terms of stimulus contour and ocular torsion.     

Feature-based attention resolves depth ambiguity

Perceiving the world around us requires that we resolve ambiguity. This process is often studied in the lab using ambiguous figures whose structures can be interpreted in multiple ways. One class of figures contains ambiguity in its depth relations, such that either of two surfaces could be seen as being the “front” of an object. Previous research suggests that selectively attending to a given location on such objects can bias the perception of that region as the front. This study asks whether selectively attending to a distributed feature can also bias that region toward the front. Participants viewed a structure-from-motion display of a rotating cylinder that could be perceived as rotating clockwise or counterclockwise (as imagined viewing from the top), depending on whether a set of red or green moving dots were seen as being in the front. A secondary task encouraged observers to globally attend to either red or green. Results from both Experiment 1 and 2 showed that the dots on the cylinder that shared the attended feature, and its corresponding surface, were more likely to be seen as being in the front, as measured by participants’ clockwise versus counterclockwise percept reports. Feature-based attention, like location-based attention, is capable of biasing competition among potential interpretations of figures with ambiguous structure in depth.     

The flash-lag phenomenon: object motion and eye movements

An object flashed briefly in a given location, the moment another moving object arrives in the same location, is perceived by observers as lagging behind the moving object (flash-lag effect). Does the flash-lag effect occur if the retinal image of the moving object is rendered stationary by smooth pursuit of the moving object? Does the flash-lag effect occur if the retinal image of a stationary object is caused to move by smooth-pursuit eye movements? A disk was briefly flashed in the center of a moving ring such that the ring center was completely 'filled' by the disk. In this display, observers perceived the flashed disk to lag such that it appeared only to partially 'fill' the ring center. The 'unfilled' portion (perceived void) of the moving ring was seen in the color of the background. With smooth pursuit of the ring, the flash-lag effect was eliminated, and observers saw the flashed disk centered on the moving ring. A strong flash-lag effect was observed when observers smoothly pursued a moving point target past a continuously visible stationary ring. Once again, the flashed disk appeared to only partially fill the center of the continuously visible stationary ring, yielding a vivid 'perceived void'. These results are discussed in terms of neural delays and their compensation.     

Absence of color-selectivity in Duncker-type induced visual movement

Using a stationary target and moving field, both consisting of gratings of vertical light and dark bars, Over and Lovegrove (1973) reported that, with monoptic viewing, induced target movement is weaker when the light bars of the two components are different in color. This reduction did not occur for dichoptic viewing, for which the aftereffect was almost negligible. Six experiments are described. The effect of different colors was not confirmed, using a stationary point and moving frame or stationary and moving gratings. Reduced effects for different colors and greatly reduced effects for dichoptic viewing occurred only when there was a stationary boundary to the moving bars of the field grating, as in Over and Lovegrove’s experiment. It is concluded that the effect studied by Over and Lovegrove is not the classical induced movement described by Duncker (1929/1938) but one due to periodic coincidence and noncoincidence of moving and stationary bars in grating patterns. This effect is absent when target and field bars are rendered more distinguishable by different colors.     

Rotation of Water in the Morris Water Maze Interferes with Path Integration Mechanisms of Place Navigation

The idea that place navigation in the Morris water maze is implemented by path integration between locations determined by landmark sighting was investigated in a 200-cm-diameter pool in which circular (7.2°/s) motion of water could be induced by tangentially arranged water jets. The rats were trained at 8 trials per day to navigate to an erectable platform which was raised after the rat had spent a criterion time in the target annulus (30 cm in diameter) in the midpoint of the NW quadrant. Asymptotic escape latency of 7 s was reached after 9 days in moving water (n= 8) and after 6 days in stationary water (n= 8). The group overtrained for 13 days in stable water performed well even after it was transferred to moving water. Changing the sense of rotation of water from counterclockwise to clockwise did not affect the asymptotic performance. The above findings show that overtrained rats rely on landmark sighting rather than on path integration. The influence of water movement reappeared when place navigation to a new target (SW) was examined in alternating 2-s periods of light (L) and darkness (D). On the first day, the latencies were 15.2 ± 1.2 and 22.8 ± 1.9 s in stable and moving water, respectively, but dropped to 10 s on the following day. The tracks generated in the L period were more tortuous than those generated in the D period and this difference was more pronounced in moving than in stable water. It is concluded that path integration mechanisms supporting navigation during intervals of darkness are impaired in moving water but that this impairment disappears in overtrained animals.     

The flash-lag effect during illusory chopstick rotation

In the 'flash-lag' effect, a static object that is briefly flashed next to a moving object appears to lag behind the moving object. A flash was put up next to an intersection that appeared to be moving clockwise along a circular path but was actually moving counterclockwise [the chopstick illusion; Anstis, 1990, in AI and the Eye Eds A Blake, T Troscianko (London: John Wiley) pp 105 117; 2003, in Levels of Perception Eds L Harris, M Jenkin (New York: Springer) pp 90 93]. As a result, the flash appeared displaced clockwise. This was appropriate to the physical, not the subjective, direction of rotation, and it suggests that the flash-lag illusion occurs early in the visual system, before motion signals are parsed into moving objects.     

Color-selectivity in simultaneous motion contrast

Thirty-two Ss were required to estimate the apparent motion of stationary vertical lines viewed against a background of moving vertical lines when both patterns were seen by the same eye (monoptic conditions) or the center pattern was seen by one eye and the surrounds by the other eye (dichoptic conditions). The stationary lines appeared to be moving from right to left as the surrounds moved left to right. The simultaneous motion contrast found under monoptic conditions was maximal when the center pattern and the surrounds were the same color and was reduced when they differed in color. The surrounds had limited influence on the apparent motion of the center section under dichoptic condition, and the color relationship was no longer important. Related color selectivity has been reported for the motion aftereffect (successive motion contrast), and both sets of data can be attributed to inlaibitory interaction (simultaneous in one case and successive in the other) among neural detectors tuned to wavelength as well as the direction of image motion.     

Consciousness mediated by neural transition states: How invisibly rapid motions can become visible

When observers view a rapidly moving stimulus they may see only a static streak. We report that there can be a transient percept of motion if such a moving stimulus is preceded or followed by a stationary image of that stimulus. A ring of dots was rotated so rapidly observers only saw a continuous outline circle and could not report its rotation direction. When an objectively stationary ring of dots preceded or followed this rotating ring, the stationary ring appeared to visibly launch into motion from a standstill or visibly rotate to a halt, principally in the same direction as the actual rapid rotation. Thus, motions too rapid to be consciously perceived as motion can nonetheless be processed by the visual system, and generate neural transition states that are consciously experienced as motion percepts. We suggest such transition states might serve a unifying function by bridging discontinuous motion states.     

The apparent paths of two or three circularly moving spots

Summary Two or three circularly moving luminous spots presented side by side in a dark room were observed under non-restrictive conditions, instead of pursuing a particular spot with the eyes. The experimental variables were speed, direction (clockwise or counterclockwise) and the phase difference between the moving spots. The paths of the circularly moving spots appeared to be a circle, an ellipse, or a straight line. With the three phase differences of 0°, 90°, and 180°, the paths appeared to be horizontally, obliquely, and vertically elongated ellipses, respectively. The direction difference from the other moving spots could affect the size of the apparent path. The speed had the most remarkable effect on the apparent paths. The perceptual vector analysis is applicable under slow speed conditions in the present experiments with a display of relatively large visual angle.This study was conducted in The Psychological Laboratory, Keio University in Yokohama     

Anomalous spiral aftereffects: a new twist to the perception of rotating spirals.

Stationary spirals viewed after inspecting rotating sectored disks appear to rotate and to expand or contract radially, even though the rotating disks contain no perceptible components of radial motion. Moreover, the relative directions of illusory rotation and radial motion observed in these instances are 'impossible' under the stimulus constraints normally imposed by the geometry of a spiral under rotation: the stationary spirals appeared to expand/contract in directions opposite to those normally observed under conditions of actual spiral rotation, and under conditions of illusory spiral rotation in classical spiral aftereffects.     

Induced rotation with concentric patterns

Duncker (1929) described induced rotation of a radial-line pattern when a concentric, enclosing annulus pattern rotated. This observation has not, so far, been confirmed or extended. Six experiments are described. The results from Experiments 1 and 2 showed that the frequency with which induced rotation is reported during standard observation periods is not affected by either angular velocity up to 15 deg/sec or unpatterned gaps up to 5 deg wide between the inner and outer patterns. Experiment 3 confirmed that the strength of the effect can be satisfactorily measured by cancellation of induced movement. Experiments 4–6 showed that induced rotation is very weak or absent when the inner disk rotates and the concentric annulus is stationary, increases in velocity as the number of radial lines in the rotating annulus increases by up to half the number in the stationary disk, and is only slightly stronger when the area of contrast between moving and stationary lines is poorly resolved in the peripheral visual field. The results are considered in terms of the resolution in perception of displacement ambiguity between moving and stationary elements.     

Left-right visual field asymmetry in bistable motion perception

Twelve observers viewed two alternating frames, each consisting of three rectangular bars which were displaced laterally by one cycle in one frame with respect to the other. At long interframe intervals (IFIs) observers perceived a group of three elements moving as a whole (group movement), whereas with IFIs shorter than 40-60 ms the overlapping elements in each frame appeared stationary while the third element appeared to move from one end of the display to the other (end-to-end movement). The percentage of group movement responses in central viewing was compared to those obtained for stimulus presentation in the left and right visual fields (4 deg eccentricity), for opposite horizontal directions of motion. All ten right-handed subjects showed a left-field advantage in sensitivity to group movement. The two left-handed subjects showed a similar advantage in sensitivity with right-field presentation. The effects of monocular vision, hand used in the task, spatial frequency, and contrast on visual field asymmetry were all investigated in two right-handed subjects. None of these factors affected the left-right asymmetry.     

After effect of seen movement: Evidence for peripheral and central components

Three experiments showed that the movement after-effect (MAE) contains both peripheral and central components. In Experiment I, the left eye viewed a sectored disc rotating to the left, and the right eye viewed a disc rotating to the right, on corresponding retinal areas. Result: when each eye in turn then viewed a stationary disc, the left eye saw a MAE to the right, and the right eye a MAE to the left. These MAE_s must be peripheral.

In Experiment II, it was arranged that the movement information was shared out between the eyes, using a ring of lights which were switched on and off to give rotating phi movement. It was arranged that each eye on its own saw a random flashing oscillation but the two eyes together saw rotation anticlockwise. Result: a clockwise MAE was seen, which must be central.

In Experiment III, the switching programme was modified to arrange that now each eye on its own saw rotation clockwise, but the two eyes together saw rotation anticlockwise. Result: a clockwise MAE was seen, which must be central. (Peripheral MAE_s from each eye on its own would have been anticlockwise.)     

Foreground and background in dynamic spatial orientation

The dependency of visually induced self-motion sensation upon the density of moving contrasts as well as upon additional stationary contrasts in the foreground or background was investigated. Using two different optokinetic stimuli, a disk rotating in the frontoparallel plane, and the projection of horizontally moving stripes onto a cylindrical screen, it was found that: (1) visually induced self-motion depends upon the density of moving contrasts randomly distributed within the visual field and, with a single contrast area of 1/4 %, is saturated when about 30% of the visual field is moving; (2) additional stationary contrasts inhibit visually induced serf-motion, proportional to their density; and (3) the location in depth of the stationary contrasts has a significant effect upon this inhibition. Their effect is considerable when located in the background of the moving stimuli but weak when appearing in the foreground. It is concluded that dynamic visual spatial orientation relies mainly on information from the seen periphery, both retinal and depth.     

Colored aftereffects produced with moving edges

Colored aftereffects that lasted as long as 6 weeks were produced with moving patterns of parallel black and white stripes or with black and white spirals. During adaptation, the patterns moved periodically in opposite directions, each direction paired with one illuminant, red or green. When the moving patterns were later viewed in white light, S saw the red and green colors, but they were related in the opposite way to the direction of motion. The red and green aftereffects were also produced by other pairs of illuminants, red and white, white and green, reddish-yellow and white, and white and greenish-yellow. The aftereffects did not occur unless, during adaptation, the stripes moved in both directions, each direction paired with a different color. The aftereffect was elicited by stripe motion over the retina—it was seen when the eye swept over a pattern of stationary stripes. The aftereffect desaturated when the retinal orientation of the stripes was changed from the adaptation orientation. Saturation was increased by longer exposure and slower speed during adaptation and by faster speed and a more rapid rate of altemation during the test. The luminance of the adaptation light seemed to have little effect. The aftereffect did not transfer from one eye to the other, and it did not change retinal locus, as was shown when clear images of a colored square that lasted several days were produced with a spiral. S ftxated the spiral’s center. The spiral rotated altemately in opposite directions. A red square with a green surround was projected on the center of the spiral when it rotated in one direction; a green square with a red surround was used when it rotated in the other direction. Following 50 min of adaptation, colored images of the squares were seen when the center of the spiral was ftxated and the direction of     

Detection of color in rotating objects by infants and its generalization over changes in velocity.

In three experiments, infants between 8 and 20 weeks of age were familiarized during habituation trials to either a stationary or revolving patterned cylinder (Experiment 1) or to the same object when it was revolving at one of two angular velocities (Experiments 2 and 3). In the postfamiliarization trials, angular velocity was changed with the color of the pattern either the same as or different from that in the familiarization trials. The results showed that the infants were not only sensitive to movement and changes in velocity but to the color of the moving pattern. Furthermore, this response to color generalized across changes in angular velocity. These findings indicate that a necessary condition for identity constancy, detection of an object property with object transformations, is present between 8 and 20 weeks, prior to the stage of manual manipulation of objects. A number of subsidiary findings concerning movement discrimination at 55 and 100 cm viewing distances by 11- and 17-week-old infants are also described.     

Top-down controlled, delayed selection in the attentional blink

In a previous study, it was shown that the attentional blink (AB)--the failure to recall the 2nd of 2 visual targets (T1 and T2) presented within 500 ms in rapid serial visual presentation--is reduced when T2 is preceded by a distractor that shares a feature with T2 (e.g., color; Nieuwenstein, Chun, van der Lubbe & Hooge, 2005). Here, this cuing effect is shown to be contingent on attentional set. For example, a red distractor letter preceding a green digit T2 is an effective cue when the task is to look for red and green digits, but the same red cue is relatively ineffective when the task is to look for only green digits or when the color of T2 is not specified. It is also shown that cuing is not interrupted by a distractor intervening between the cue and T2. These findings provide evidence for a contingent, delayed selection account of the AB.     

Fast Responses of the Human Hand to Changes in Target Position

If a target toward which an individual moves his hand suddenly moves, he adjusts the movement of his hand accordingly. Does he use visual information on the target's velocity to anticipate where he will reach the target? These questions were addressed in the present study. Subjects (N = 6 in each of 4 experiments) were instructed to hit a disk with a rod as soon as it appeared on a screen. Trajectories of the hand toward stationary disks were compared with those toward disks that jumped leftward or rightward as soon as the subject's hand started moving toward the screen, and with those in which either the disk or the background started moving leftward or rightward. About 110 ms after the disk was suddenly displaced, the moving hand was diverted in the direction of the perturbation. When the background moved, the disk's perceived position shifted in the direction in which the background was moving, but the disk appeared to be moving in the opposite direction. When hitting such disks, subjects adjusted their movement in accordance with the perceived position, rather than moving their hand in the direction of the perceived motion in anticipation of the disk's future displacement. Thus, subjects did not use the perceived velocity to anticipate where they would reach the target but responded only to the change in position