Biomedical subjects

P-J Hsieh

Publications and source records attributed to P-J Hsieh.

8 recordsLinked to original sources

PubMed2006

Microsaccade directions do not predict directionality of illusory brightness changes of overlapping transparent surfaces.

Tse (2005) recently introduced a new class of illusory brightness changes where shifts of attention lead to shifts in perceived brightness across overlapping, transparent figures, under conditions of visual fixation. In the absence of endogenous attentional shifts, illusory brightness changes appear to shift from figure to figure spontaneously, much as occurs in other multistable phenomena. The goal of the present research is to determine whether fixational microsaccades are correlated with perceived brightness changes. It has recently been demonstrated that microsaccades can reveal the direction of covert attentional shifts either toward (Engbert, R. & Kliegl, R. (2003). Microsaccades uncover the orientation of covert attention. Vision Research, 43, 1035-1045; Hafed, Z. M. & Clark, J. J. (2002). Microsaccades as an overt measure of covert attention shifts. Vision Research, 42(22), 2533-2545) or away from (Rolfs, M., Engbert, R., & Kliegl, R. (2004). Microsaccade orientation supports attentional enhancement opposite a peripheral cue: commentary on Tse, Sheinberg, and Logothetis (2003). Psychological Science, 15(10), 705-707) a peripheral cue under certain circumstances. Others (Horwitz, G. D. & Albright, T. D. (2003). Short-latency fixational saccades induced by luminance increments. Journal of Neurophysiology, 90(2), 1333-1339; Tse, P. U., Sheinberg, D. L., & Logothetis, N. K. (2002). Fixational eye movements are not affected by abrupt onsets that capture attention. Vision Research, 42, 1663-1669; Tse, P. U., Sheinberg, D. L., & Logothetis, N. K. (2004). The distribution of microsaccade directions need not reveal the location of attention. Psychological Science, 15(10), 708-710) found no change in the distribution of microsaccade directions as a function of where attention is allocated, although changes in the rate of microsaccades were observed in all of these studies in response to the onset of attentional reallocation. It is therefore possible that the distribution of microsaccade directions will change as a function of which figure is perceived to darken, or that changes in this distribution predict which figure will subsequently darken. We find no correlation between this distribution and which figure undergoes the effect, and therefore conclude that microsaccade directionality is not influenced by and does not influence which figure undergoes the effect. Moreover, the directions of microsaccades that occur immediately prior to a perceptual switch are not correlated with the perceived position of the figure that undergoes the effect. However, we do find that the rate of microsaccades decreases upon a perceptual switch, signifying an attentional shift coincident with the perceptual shift. We conclude that microsaccade directionality does not determine, predict, or cause which figure will subsequently be perceived to undergo an illusory brightness change.

Adaptation, Ocular↗

PubMed2006

The infinite regress illusion reveals faulty integration of local and global motion signals.

We report a new visual illusion, where a global shape appears to continually move away from fixation, even though it remains a fixed distance from fixation. The illusion occurs because local motion signals within the object indicate motion away from fixation, and are incorrectly attributed by the visual system to the motion trajectory of the global object. A simple weighted vector summation of global and local motion signals, while a reasonable first approximation, cannot fully account for our data. We show that the faster the local motion signal, the more it biases judgments of global motion direction. We propose that local and global motion signals are summed non-linearly for this stimulus because as local motion speed increases, moving luminance blobs are visible for less time, affording less time to inhibit inappropriate component motion signals. This effect reveals the degree to which the visual system can incorrectly combine local and global motion signals belonging to a single object.

Adult↗

PubMed2006

Bistable illusory rebound motion: Event-related functional magnetic resonance imaging of perceptual states and switches.

The neural correlates of a recently discovered visual illusion that we call 'illusory rebound motion' (IRM) are described. This illusion is remarkable because motion is perceived in the absence of any net motion energy in the stimulus. When viewing bars alternating between white and black on a gray background, the percept alternates between one of flashing bars (veridical) and the IRM illusion, where the bars appear to shoot back and forth rather like the opening and closing of a zipper. The event-related functional magnetic resonance imaging (fMRI) data reported here reveal that (1) the blood-oxygen-level-dependent (BOLD) signal in the human analog of macaque motion processing area MT (hMT+) increases when there is a perceptual change from "no-IRM" to "see-IRM" and decreases when there is a perceptual change from "see-IRM" to "no-IRM," although the stimulus remains constant; and (2) the BOLD signal in early retinotopic areas (V1, V2, and V3d) shows switch-related activation whenever there is a perceptual change, regardless whether from IRM to no-IRM or vice versa. We conclude that hMT+ is a neural correlate of this novel illusory motion percept because BOLD signal in hMT+ modulates with the perception of IRM.

Adolescent↗

PubMed2006

Mechanisms underlying the perceived angular velocity of a rigidly rotating object.

The perceived angular velocity of an ellipse undergoing a constant rate of rotation will vary as its aspect ratio is changed. Specifically, a "fat" ellipse with a low aspect ratio will in general be perceived to rotate more slowly than a "thin" ellipse with a higher aspect ratio. Here we investigate this illusory underestimation of angular velocity in the domain where ellipses appear to be rotating rigidly. We characterize the relationship between aspect ratio and perceived angular velocity under luminance and non-luminance-defined conditions. The data are consistent with two hypotheses concerning the construction of rotational motion percepts. The first hypothesis is that perceived angular velocity is determined by low-level component-motion (i.e., motion-energy) signals computed along the ellipse's contour. The second hypothesis is that relative maxima of positive contour curvature are treated as non-component, form-based "trackable features" (TFs) that contribute to the visual system's construction of the motion percept. Our data suggest that perceived angular velocity is driven largely by component signals, but is modulated by the motion signals of trackable features, such as corners and regions of high contour curvature.

Form Perception↗

PubMed2006

Illusory color mixing upon perceptual fading and filling-in does not result in 'forbidden colors'.

A retinally stabilized object readily undergoes perceptual fading. It is commonly believed that the color of the apparently vanished object is filled in with the color of the background because the features of the filled-in area are determined by features located outside the stabilized boundary. Crane, H. D., & Piantanida, T. P. (1983) (On seeing reddish green and yellowish blue. Science, 221, 1078-1080) reported that the colors that are perceived upon full or partial perceptual fading can be 'forbidden' in the sense that they violate color opponency theory. For example, they claimed that their subjects could perceive "reddish greens" and "yellowish blues." Here we use visual stimuli composed of spatially alternating stripes of two different colors to investigate the characteristics of color mixing during perceptual filling-in, and to determine whether 'forbidden colors' really occur. Our results show that (1) the filled-in color is not solely determined by the background color, but can be the mixture of the background and the foreground color; (2) apparent color mixing can occur even when the two colors are presented to different eyes, implying that color mixing during filling-in is in part a cortical phenomenon; and (3) perceived colors are not 'forbidden colors' at all, but rather intermediate colors.

Adult↗

PubMed2006

Stimulus factors affecting illusory rebound motion.

Stimulus attributes that influence a recently reported illusion called "illusory rebound motion" (IRM; [Hsieh, P.-J., Caplovitz, G. P., & Tse, P. U. (2005). Illusory rebound motion and the motion continuity heuristic. Vision Research, 45, 2972-2985.]) are described. When a bar alternates between two different colors, IRM can be observed to traverse the bar as if the color were shooting back and forth like the opening and closing of a zipper, even though each color appears in fact all at once. Here, we tested IRM over dynamic squares or disks defined by random dot or checkerboard textures to show that (1) IRM can be perceived in the absence of first-order motion-energy (or when the direction of net first-order motion-energy is ambiguous); (2) the direction of IRM is multistable and can change spontaneously or be changed volitionally; and (3) the perceived frequency of IRM is affected by several factors such as the contours of the stimulus, stimulus texture, and motion-energy.

Artifacts↗

PubMed2005

Illusory motion induced by the offset of stationary luminance-defined gradients.

An illusory motion induced by the offset of a stationary gradient stimulus is characterized. When a gradient stimulus, whose luminance contrast ranges gradually from white on one side to black on the other, is made to disappear all at once so that only the uniform white background remains visible, illusory motion is perceived. This motion lasts approximately 700 ms, as if the stimulus moves from the low to the high luminance contrast side. This gradient-offset induced motion does not occur for equiluminant color-defined gradient offsets, suggesting that it relies mainly on the magnocellular pathway. Our data are consistent with the hypothesis that this illusion is caused by the decay of the gradient afterimage.

Afterimage↗

PubMed2005

Illusory rebound motion and the motion continuity heuristic.

A new motion illusion, "illusory rebound motion" (IRM), is described. IRM is qualitatively similar to illusory line motion (ILM). ILM occurs when a bar is presented shortly after an initial stimulus such that the bar appears to move continuously away from the initial stimulus. IRM occurs when a second bar of a different color is presented at the same location as the first bar within a certain delay after ILM, making this second bar appear to move in the opposite direction relative to the preceding direction of ILM. Three plausible accounts of IRM are considered: a shifting attentional gradient model, a motion aftereffect (MAE) model, and a heuristic model. Results imply that IRM arises because of a heuristic about how objects move in the environment: In the absence of countervailing evidence, motion trajectories are assumed to continue away from the location where an object was last seen to move.

Color Perception↗