The microgenesis of illusory figures: evidence for visual hypothesis testing.
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In previous work with a neural-network model of boundary segmentation and reset, the percept of persistence was linked to the duration of a boundary segmentation after stimulus offset. In particular, the model simulated the decrease of persistence duration with an increase in stimulus duration and luminance. Further evidence is revealed for the neural mechanisms involved in the theory. Simulations show that the model reset signals generate orientational afterimages, such as the MacKay effect, when the reset signals can be grouped by a subsequent boundary segmentation that generates illusory contours through them. Simulations also show that the same mechanisms explain properties of residual traces, which increase in duration with stimulus duration and luminance. The model hereby discloses previously unsuspected mechanistic links between data about persistence and afterimages, and helps to clarify the sometimes controversial issues surrounding distinctions between persistence, residual traces, and afterimages.
A random-dot field undergoing counterphase flicker paradoxically appears to move in the same direction as head and eye movements, i.e. opposite to the optic-flow field. The effect is robust and occurs over a wide range of flicker rates and pixel sizes. The phenomenon can be explained by reversed phi motion caused by apparent pixel movement between successive retinal images. The reversed motion provides a positive feedback control of the display, whereas under normal conditions retinal signals provide a negative feedback. This altered polarity invokes self-sustaining eye movements akin to involuntary optokinetic nystagmus.
The relationship between apparent size and apparent distance is given by Emmert's law, which states that a retinal image is proportional in size to the distance of the surface it is projected upon. This principle also applies to retinal afterimages in that they, too, will change in apparent size if distance cues suggest that the location of the object onto the retinal image has been altered. It has also been known for some time that non-retinal cues can produce quantitative and qualitative effects on an afterimage when it is viewed in the dark. In the present two studies, positive afterimages of an observer's hand, as well as objects held by that hand, were used as targets to investigate the effects on size-constancy scaling of moving the hand to and fro along the line of sight for different distances in the dark. Results show that, when observers focus on a held object, the changes in size predicted by Emmert's law occur in response to both active and passive proprioceptive or haptic cues. The most intriguing result consisted of the finding that, when only the hand is the target, there appears to be a limit to the decrease in apparent hand size. It appears that the visual system 'refuses' to size-scale the hand below a limit it accepts as representative or acceptable of 'its' hand.
We apply an adaptation technique to explore the neural code for the visual location of textures defined by modulation of orientation over space. In showing that adaptation to textures modulated around one orientation shifts the perceived location of textures modulated around a different orientation, we demonstrate the existence of a neural code for the location of orientation change that generalises across orientation content. Using competitive adaptation, we characterise the neural processes underlying this code as single-opponent for orientation, that is with concentric excitatory/inhibitory receptive areas tuned to a single orientation.
The effect of voluntary attention on afterimage fragmentation was explored in two experiments. The afterimage, in the form of a 30 degrees-tilted star of David, was generated after prolonged steady fixation in the first experiment, and with a brief and intense flash in the second experiment. Subjects were instructed to select various target shapes in the afterimage for attention and, at the same time, observe what was visible or invisible. Verbal reports and manual responses to afterimage changes were analyzed. Attended shapes were found to disappear from awareness Faster than unattended ones (experiment 1), and complementary shapes were found to predominate visual awareness when one of the pair was selected for attention (experiment 2). Voluntary attention was also found to affect closure (filling-in of enclosed regions) and smoothing of line figures in afterimages.
I report evidence for a purely temporal perceptual transparency mechanism. Rapid alternation of two images in the same location can result in the simultaneous experience of both, accompanied by a sense of transparency. This is true even when the sum of the two images does not appear transparent, which suggests that the percept is not mediated by the static transparency processes. At slow rates, alternating gratings were experienced as successive. As the rate was increased, by 8 Hz observers experienced the gratings as simultaneous. The rapidly alternating gratings are apparently processed separately before being combined for awareness by a process that integrates over about 120 ms. A final experiment tested whether the common presentation time of different parts of an image in alternation with another would cause the parts to perceptually bind. Observers did not distinguish between a rapidly alternating intact grating display and one in which halves of the display were exchanged in time. In other words, temporal binding across space did not occur. The temporal transparency phenomenon, in addition to informing theories of transparency and the dynamics of visual processing, may also be useful for the creation of transparent displays for electronic devices.
Phenomena associated with 'central visual persistences' (CPs) are new to both medical and psychological literature. Five subjects have reported similar CPs: positive afterimages following brief fixation of high-contrast objects or drawings and eye closure. CPs duplicate shapes and colors of single objects, lasting for about 15 s. Unlike retinal afterimages, CPs do not move with the eyes but are stable in extrapersonal space during head or body rotations. CPs may reflect sustained neural activity in neurons of association cortex, which mediate object perception. A remarkable finding is that CPs can be moved in any direction by the (unseen) hand holding the original seen object. Moreover, a CP once formed will 'jump' into an extended hand and 'stick' in that hand as it moves about. The apparent size of a CP of a single object is determined by the size of the gap between finger and thumb, even when no object is touched. These CPs can be either magnified or minified via the grip of the extended hand. The felt orientation of the hand-held object will also determine the orientation of the CP seen in that hand. Thus, kinesthetic signals from hand and arm movements can determine perceived location, size, and orientation of CPs. A neural model based on physiological studies of premotor, temporal, parietal, and prefrontal cortices is proposed to account for these novel phenomena.
In an earlier paper, kinesthetic effects on central visual persistences (CPs) were reported, including the ability to move these images by hand following eye closure. While all CPs could be translated anywhere within the frontal field, the present report documents a more selective influence of manual rotations on CPs in the same subjects. When common objects or figures drawn on cards were rotated (while holding one end of the object or one corner of a card between thumb and forefinger), it was found that CPs of larger objects rotated with the hand. By contrast, CPs of smaller objects, parts of objects, and textures remained stable in space as the hand rotated. It is proposed that CPs of smaller stimuli and textures are represented mainly by the ventral stream (temporal cortex) while larger CPs, which rotate, are represented mainly by the dorsal stream (parietal cortex). A second discovery was that CPs of small objects (but not of line segments or textures) could be rotated when the thumb and fingers surrounded the edges of the object. It is proposed that neuronal convergence of visual and tactile information about shape increases parietal responses to small objects, so that their CPs will rotate. Experiments with CPs offer new tools to infer visual coding differences between ventral and dorsal streams in man.
Sequential viewing of two orthogonally related patterns produces an afterimage of the first pattern (Vidyasagar et al, 1999 Nature 399 422-423; Francis and Rothmayer, 2003 Perception and Psychophysics 65 508-522). We investigated how the timing between the first stimulus (a vertical bar grating) and the second stimulus (a horizontal bar grating) affected the visibility of the afterimage (a perceived vertical grating). As the duration from offset of the first stimulus increased, reports of afterimages decreased. Holding fixed the total time from offset of the first stimulus and increasing the duration from offset of the second stimulus while decreasing the time between the first and second stimuli, caused a decrease in afterimage reports. We interpret this finding in terms of Grossberg's BCS - FCS (boundary contour system--feature contour system) theory. In this theory, the afterimage percept is the result of color complement after-responses in the FCS system interacting with orientation after-responses in the BCS system. The two types of after-responses interact at a stage of neural filling-in to produce the afterimage percept. As the duration between the stimuli increases, the color after-responses weaken so that visible filling-in is less likely to occur. A similar effect occurs for the orientation after-responses but at a faster time scale. Simulations of the model match the experimental data.
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After-effects of human-computer interaction (HCI) were investigated by using the P300 component of the event-related brain potential (ERP). Forty-nine subjects (naive non-users, beginners, experienced users, programmers) completed three paper/pencil tasks (text editing, solving intelligence test items, filling out a questionnaire on sensation seeking) and three HCI tasks (text editing, executing a tutor program or programming, playing Tetris). The sequence of 7-min tasks was randomized between subjects and balanced between groups. After each experimental condition ERPs were recorded during an acoustic discrimination task at F3, F4, Cz, P3 and P4. Data indicate that: (1) mental after-effects of HCI can be detected by P300 of the ERP; (2) HCI showed in general a reduced amplitude; (3) P300 amplitude varied also with type of task, mainly at F4 where it was smaller after cognitive tasks (intelligence test/programming) and larger after emotion-based tasks (sensation seeking/Tetris); (4) cognitive tasks showed shorter latencies; (5) latencies were widely location-independent (within the range of 356-358 ms at F3, F4, P3 and P4) after executing the tutor program or programming; and (6) all observed after-effects were independent of the user's experience in operating computers and may therefore reflect short-term after-effects only and no structural changes of information processing caused by HCI.
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A rectangularity postulate has been used in algorithms for the purpose of interpreting two-dimensional representations of rectilinear objects. This rectangularity postulate may affect the perception of true surfaces. In this study, rectangular surfaces and trapezoidal surfaces--the latter simulating the horizontal slant-in-depth of the rectangular surfaces--were viewed under static-monocular, moving-monocular, and static-binocular conditions, both with and without a background pattern. The static-binocular condition elicited the greatest number of accurate responses. The moving-monocular condition did not elicit significantly more accurate responses than the static-monocular viewing condition did. The effect of background pattern was insignificant. These results were unexpected in terms of ecological validity and (regarding moving-monocular viewing) because of the importance of the role of relative visual motion in the detection of object motion. However, the results are consistent with the perception of depth separation of two discrete objects.
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