The
sensation of motion is produced by stimulation of neural motion sensors at different retinal positions (van Santen & Sperling,
1985). However, the perception of motion requires a parsing and segmentation of the local motion signals. This work describes the perception of some outline figures rotating behind a sunburst pattern of 24 thin, stationary radial slits. The slits break the figures up into moving dots but the patterns of dots are ambiguous in various ways. Results reveal competing mental tendencies to organize motions globally, especially at low speeds, or locally, especially at higher speeds. Moreover, the absolute motion paths of the dots are often unavailable to consciousness because they are preempted by perceptual parsing into patterns of relative motion.
Some earlier studies on rotating patterns used no apertures or occluders at all; some have used large square apertures; and some have used translation behind stationary slits. Among studies without apertures, Farrell and Shepard (
1981) examined apparent rotational motion in polygonal shapes ranging in rotational symmetry from random to self-identical under 180-deg rotation. Observers adjusted the rate of alternation between two computer-displayed orientations of a polygon to determine the critical time at which rigid rotation broke down into nonrigid deformation. For asymmetric polygons, this critical time increased linearly with orientational disparity, consistent with Korte’s third law of motion. For nearly symmetric polygons, however, the critical time increased markedly as the disparities approached 180 deg, because of the availability of a shorter, nonrigid rotation in the opposite direction. The results demonstrate the existence of competing mental tendencies to preserve the rigid structure of an object and to traverse a minimum transformational path. Weiss and Adelson (
2000) examined rotating ellipses. They found that narrow ellipses appeared to rotate, whereas fat ellipses appeared to deform in a gelatinous way. Adding four moving dots just outside the perimeter of the ellipse controlled the perceived motion: If the dots rotated, the ellipse also appeared to rotate, whereas if the dots moved in and out radially the ellipse appeared to deform. The results failed to fit computational models that pool constraints over a local area only, models that propagate information along contours, or models that indiscriminately propagate information across space. The authors proposed that the visual system splits the visual display into layers and then applies smoothness motion constraints to each layer separately. For instance, when an ellipse rotated in front of a pattern of drifting random dots, the ellipse and the dots are first split apart by perceptual scission and then their motions are analyzed separately. Sparrow and Stine (
1998) studied the perception of the shadows of rotating eight-vertex geometric forms.
Shiffrar and her coworkers moved lines and figures around behind a
pertures. They found that observers consistently perceived the fixed center of rotation for an unmarked line viewed through an aperture as located on the line, regardless of its actual location. Accuracy greatly improved with visible line endings. This finding was extended to explain why a square appeared nonrigid when it rotated behind four occluding portholes, each porthole being about half as wide as the square. The square appeared to expand when its corners were visible and to shrink when they were hidden, and only parts of the straight sides were visible. Observers seemed unable to apply an object rigidity constraint across apertures (Shiffrar & Pavel,
1991; Meyer & Dougherty,
1990).
In other experiments the square moved around a circular path without rotating, like the sponge in the hand of a window cleaner. When the corners were hidden, and only straight sides were visible through the four portholes, each straight side was ambiguous because of the aperture problem, and again observers were unable to integrate across the four apertures to see a rigid square. Strangely, integration was much better when the sides were not clearly seen, for instance, when they were low in contrast or viewed peripherally (Lorenceau & Shiffrar,
1992; Shiffrar & Lorenceau,
1996).
There have been many studies of shapes that translate rapidly behind a
single slit (e.g., Casco & Morgan,
1984). Morgan, Findlay, and Watt (
1982) have reviewed this literature. Observers often report seeing the whole shape, compressed along its axis of movement but surprisingly much broader than the narrow viewing slit. Opinion is still divided on whether this is a mundane case of retinal painting caused by eye movements (Anstis & Atkinson,
1967) or whether the visual system is able to integrate successive visual snapshots as they arrive, a slitful at a time (Nishida,
2004).
In this study, outlined shapes always rotated behind stationary,
multiple, thin slits. Bruno and Bertamini (
1990) studied the perception of surface contours specified by occlusion events that varied in density, velocity, and type of motion (rotation or translation). Their observers viewed either a square rotating behind stationary slits, as we did, or else slits rotating in front of a stationary square. Observers had to report whether the square had straight or curved edges. Performance increased with rotation speed and with number of visible points, that is, the number of slits. Puzzlingly, they found that performance was far better for rotating slits than for rotating squares; the reasons for this were not clear. Nishida (
2004) displayed moving targets behind a virtual “picket fence” that obscured the scene except for thin slits between the pickets. Observers could read wide alphanumeric characters that moved behind these narrow slits, even during strict fixation, clearly relying upon spatiotemporal integration within the motion system. Using an adaptation of the reverse-correlation technique, he showed that the spatial frequencies used for the letter-recognition task were higher than the limit imposed by spatial sampling through the slits, and thus were only available by temporal information (Burr & Ross,
2004). This provides clear evidence against the notion of separate analysis of motion and pattern. Instead, motion mechanisms integrate spatial pattern information along the trajectory of pattern movement to obtain clear perception of moving patterns. The pattern integration mechanism is probably a direction-selective filtering by V1 simple cells, but the integration of the local pattern information into a global figure may be guided by a higher order motion mechanism such as MT pattern cells.
For completeness, we refer to an interesting study by Bruno and Gerbino (
1991), whose stimuli were somewhat like ours, although they studied quite different perceptual effects. In their display, an invisible white triangle on a white surround occluded a set of black lines radiating from a point behind the center of the triangle. This illusory triangle occluded the lines rather as Kanisza’s illusory square occludes four pacmen. When the line pattern rotated behind the stationary triangle, the triangle was easily perceived. However, if the lines kept still and the triangle rotated in front of them, observers reported only an amoeboid shape instead of a regular, rigid triangle. The authors attribute this “background superiority effect” to perceptual extraction of local kinematic information.