Size Aftereffect Research Articles

Haptic touch modulates size adaptation aftereffects on the hand.

When we interact with objects using our hands, we derive their size through our skin. Prolonged exposure to an object leads to a perceptual size aftereffect: adapting to a larger/smaller object makes a subsequently perceived object to appear smaller/larger than its actual size. This phenomenon has been described as haptic as tactile sensations with kinesthetic feedback are involved. However, the exact role of different haptic components in generating this aftereffect remains largely underexplored. Here, we investigated how different aspects of haptic touch influence size perception. After adaptation to a large sphere with one hand and a small sphere with the other, participants touched two test spheres of equal or different sizes and judged which one felt larger. Similar haptic size adaption aftereffects were observed (a) when participants repeatedly grasped on and off the adapters, (b) when they simply continued to grasp the adapters without further hand movements, and (c) when the adapters were grasped without involving the fingers. All these conditions produced stronger aftereffects than a condition where the palms were simply resting on the adapter. Our findings suggest that the inclusion of grasp markedly increased the aftereffects, highlighting the pivotal role of haptic interactions in determining perceptual size adaptation. (PsycInfo Database Record (c) 2024 APA, all rights reserved).

Object Image Size Is a Fundamental Coding Dimension in Human Vision: New Insights and Model

In previous psychophysical work we found that luminance contrast is integrated over retinal area subject to contrast gain control. If different mechanisms perform this operation for a range of superimposed retinal regions of different sizes, this could provide the basis for size-coding. To test this idea we included two novel features in a standard adaptation paradigm to discount more pedestrian accounts of repulsive size-aftereffects. First, we used spatially jittering luminance-contrast adaptors to avoid simple contour displacement aftereffects. Second, we decoupled adaptor and target spatial frequency to avoid the well-known spatial frequency shift aftereffect. Empirical results indicated strong evidence of a bidirectional size adaptation aftereffect. We show that the textbook population model is inappropriate for our results, and develop our existing model of contrast perception to include multiple size mechanisms with divisive surround-suppression from the largest mechanism. For a given stimulus patch, this delivers a blurred step-function of responses across the population, with contrast and size encoded by the height and lateral position of the step. Unlike for textbook population coding schemes, our human results (N = 4 male, N = 4 female) displayed two asymmetries: (i) size aftereffects were greatest for targets smaller than the adaptor, and (ii) on that side of the function, results did not return to baseline, even when targets were 25% of adaptor diameter. Our results and emergent model properties provide evidence for a novel dimension of visual coding (size) and a novel strategy for that coding, consistent with previous results on contrast detection and discrimination for various stimulus sizes.

Size aftereffect is non-local

It is well known that prolonged exposure to a certain size stimulus alters the perceived size of a subsequently presented stimulus at the same location. How the rest of the visual space is affected by this size adaptation, however, has not been systematically studied before. Here, to fill this gap in literature, we tested size adaptation at the adapter location as well as the rest of the visual space. We used peripherally presented solid discs (Experiment 1) and rings (Experiment 2) as adapter and target (test) stimuli. Observers adapted to a mid-sized stimulus and judged the size of the subsequently presented smaller or larger target stimuli. Results showed that the perceived sizes of target stimuli were repelled away from the adapter size, not only at the adapter location but also at other locations. These findings demonstrate that size adaptation causes widespread distortion of the visual space and alters perceived size. We discuss possible computational models that may underpin the perceptual effect.

The Thin White Line: Adaptation Suggests a Common Neural Mechanism for Judgments of Asian and Caucasian Body Size.

Visual adaptation has been proposed as a mechanism linking viewing images of thin women’s bodies with body size and shape misperception (BSSM). Non-Caucasian populations appear less susceptible to BSSM, possibly because adaptation to thin Caucasian bodies in Western media may not fully transfer to own-race bodies. Experiment 1 used a cross-adaptation paradigm to examine the transfer of body size aftereffects across races. Large aftereffects were found in the predicted directions for all conditions. The strength of aftereffects was statistically equivalent when the race of test stimuli was congruent vs. incongruent with the race of adaptation stimuli, suggesting complete transfer of aftereffects across races. Experiment 2 used a contingent-adaptation paradigm, finding that simultaneous adaptation to wide Asian and narrow Caucasian women’s bodies (or vice versa) results in no significant aftereffects for either congruent or incongruent conditions and statistically equivalent results for each. Equal and opposite adaptation effects may therefore transfer completely across races, canceling each other out. This suggests that body size is encoded by a race-general neural mechanism. Unexpectedly, Asian observers showed reduced body size aftereffects compared to Caucasian observers, regardless of the race of stimulus bodies, perhaps helping to explain why Asian populations appear less susceptible to BSSM.

A new visual illusion of aspect-ratio context

Perception of local properties of the visual field is influenced by aftereffects of adaptation. The tilt aftereffect describes repulsion of the perceived orientation of a line from the orientation of an adapting line. Analogous effects of spatial context are often called illusions. Repulsion of the perceived orientation of a grating from the orientation of a surrounding grating is referred to as the tilt illusion. In the same manner, the size aftereffect and Ebbinghaus illusion form a complementary pair of temporal and spatial context effects of size. Here we report psychophysical evidence for a previously unknown aspect-ratio illusion which causes the perceived aspect-ratio of a rectangle to be repelled from the aspect-ratio of rectangles surrounding it. This illusion provides a spatial analogue to the aspect-ratio aftereffect.

Gender and the Body Size Aftereffect: Implications for Neural Processing.

Prolonged exposure to wide (thin) bodies causes a perceptual aftereffect such that subsequently viewed bodies appear thinner (wider) than they actually are. This phenomenon is known as visual adaptation. We used the adaptation paradigm to examine the gender selectivity of the neural mechanisms encoding body size and shape. Observers adjusted female and male test bodies to appear normal-sized both before and after adaptation to bodies digitally altered to appear heavier or lighter. In Experiment 1, observers adapted simultaneously to bodies of each gender distorted in opposite directions, e.g., thin females and wide males. The direction of resultant aftereffects was contingent on the gender of the test stimulus, such that in this example female test bodies appeared wider while male test bodies appeared thinner. This indicates at least some separation of the neural mechanisms processing body size and shape for the two genders. In Experiment 2, adaptation involved either wide females, thin females, wide males or thin males. Aftereffects were present in all conditions, but were stronger when test and adaptation genders were congruent, suggesting some overlap in the tuning of gender-selective neural mechanisms. Given that visual adaptation has been implicated in real-world examples of body size and shape misperception (e.g., in anorexia nervosa or obesity), these results may have implications for the development of body image therapies based on the adaptation model.

Experimental manipulation of visual attention affects body size adaptation but not body dissatisfaction.

Prolonged exposure to large/small bodies causes aftereffects in perceived body size. Outside the laboratory, individuals repeatedly exposed to small (large) bodies tend to over- (under-) estimate their size and exhibit increased (decreased) body dissatisfaction. Why, among individuals exposed to approximately equivalent distributions of body sizes, only some develop body size and shape misperception and/or body dissatisfaction is not yet fully understood. We exposed 61 women to high and low adiposity bodies simultaneously, instructing half to attend to high, and half to low adiposity bodies. Participants in the high adiposity attention condition's perception of "normal" body size significantly increased in adiposity, and vice versa. This suggests that visual attention moderates body size aftereffects. Interventions encouraging visual attention to more realistic ranges of bodies may therefore reduce body misperception. No change in body dissatisfaction was found, suggesting that changes in the perceptual component (misperception) may not necessarily affect the attitudinal component (dissatisfaction) of body image distortion.

The Influence of Auditory Information on Visual Size Adaptation.

Size perception can be influenced by several visual cues, such as spatial (e.g., depth or vergence) and temporal contextual cues (e.g., adaptation to steady visual stimulation). Nevertheless, perception is generally multisensory and other sensory modalities, such as auditory, can contribute to the functional estimation of the size of objects. In this study, we investigate whether auditory stimuli at different sound pitches can influence visual size perception after visual adaptation. To this aim, we used an adaptation paradigm (Pooresmaeili et al., 2013) in three experimental conditions: visual-only, visual-sound at 100 Hz and visual-sound at 9,000 Hz. We asked participants to judge the size of a test stimulus in a size discrimination task. First, we obtained a baseline for all conditions. In the visual-sound conditions, the auditory stimulus was concurrent to the test stimulus. Secondly, we repeated the task by presenting an adapter (twice as big as the reference stimulus) before the test stimulus. We replicated the size aftereffect in the visual-only condition: the test stimulus was perceived smaller than its physical size. The new finding is that we found the auditory stimuli have an effect on the perceived size of the test stimulus after visual adaptation: low frequency sound decreased the effect of visual adaptation, making the stimulus perceived bigger compared to the visual-only condition, and contrarily, the high frequency sound had the opposite effect, making the test size perceived even smaller.

Size Aftereffects Are Eliminated When Adaptor Stimuli Are Prevented from Reaching Awareness by Continuous Flash Suppression.

Size aftereffects are a compelling perceptual phenomenon in which we perceive the size of a stimulus as being different than it actually is following a period of visual stimulation of an adapter stimulus with a different size. Here, we used continuous flash suppression (CFS) to determine if size aftereffects require a high-level appraisal of the adapter stimulus. The strength of size aftereffects was quantified following a 3-s exposure to perceptually visible and invisible adapters. Participants judged the size of a target that followed the adapter in comparison to a subsequent reference. Our experiments demonstrate that the adapter no longer influenced the perceived size of the subsequent target stimulus under CFS. We conclude that the perception of size aftereffects is prevented when CFS is used to suppress the conscious awarness of the adapting stimulus.

No Effect of Featural Attention on Body Size Aftereffects.

Prolonged exposure to images of narrow bodies has been shown to induce a perceptual aftereffect, such that observers’ point of subjective normality (PSN) for bodies shifts toward narrower bodies. The converse effect is shown for adaptation to wide bodies. In low-level stimuli, object attention (attention directed to the object) and spatial attention (attention directed to the location of the object) have been shown to increase the magnitude of visual aftereffects, while object-based attention enhances the adaptation effect in faces. It is not known whether featural attention (attention directed to a specific aspect of the object) affects the magnitude of adaptation effects in body stimuli. Here, we manipulate the attention of Caucasian observers to different featural information in body images, by asking them to rate the fatness or sex typicality of male and female bodies manipulated to appear fatter or thinner than average. PSNs for body fatness were taken at baseline and after adaptation, and a change in PSN (ΔPSN) was calculated. A body size adaptation effect was found, with observers who viewed fat bodies showing an increased PSN, and those exposed to thin bodies showing a reduced PSN. However, manipulations of featural attention to body fatness or sex typicality produced equivalent results, suggesting that featural attention may not affect the strength of the body size aftereffect.

Influence of Shape on the Haptic Size Aftereffect

Recently, we showed a strong haptic size aftereffect by means of a size bisection task: after adaptation to a large sphere, subsequently grasped smaller test spheres felt even smaller, and vice versa. In the current study, we questioned whether the strength of this aftereffect depends on shape. In four experimental conditions, we determined the aftereffect after adaptation to spheres and tetrahedra and subsequent testing also with spheres and tetrahedra. The results showed a clear influence of shape: the haptic aftereffect was much stronger if adaptation and test stimuli were identical in shape than if their shapes were different. Therefore, it would be more appropriate to term such aftereffects haptic shape-size aftereffects, as size alone could not be the determining factor. This influence of shape suggests that higher cortical areas are involved in this aftereffect and that it cannot be due to adaptation of peripheral receptors. An additional finding is that the geometric property or combination of properties participants use in the haptic size bisection task varies widely over participants, although participants themselves are quite consistent.

Size and shape-frequency after-effects: same or different mechanism?

Size and shape-frequency after-effects: same or different mechanism?

Probing the Uncanny Valley with the Eye Size Aftereffect

Natural human faces with abnormal visual features produce uncomfortable impressions, but artificial faces (e.g., robotic faces) do not necessarily do so. This is an example of the phenomenon called the uncanny valley. We hypothesized that this phenomenon indicates that natural and artificial faces are processed by different perceptual mechanisms, or they are processed differently by common mechanisms. We tested these hypotheses using a facial aftereffect where prolonged observation of adaptation faces with enlarged eyes induced a bias to underestimate the eye size of test faces. The results showed that adaptation to natural stimuli induced the aftereffect for both natural and artificial test stimuli. This suggests that the two types of faces engage common perceptual mechanisms. Adaptation to artificial stimuli also induced the aftereffect for natural test stimuli. However, artificial stimuli required a longer adaptation period (120 s) for the aftereffect to be induced compared to natural stimuli (60 s), suggesting that the processing of artificial faces by the human visual system may be inefficient. The uncanny valley may reflect that artificial faces are processed inefficiently by perceptual mechanisms that are common for processing natural and artificial faces.

Shape-frequency and size aftereffects: same or different mechanism?

Shape-frequency and size aftereffects: same or different mechanism?

Gaze modulation of visual aftereffects

Physiological studies of non-human primates have suggested that the direction of gaze can modulate the gain of neuronal responses to visual stimuli in many cortical areas including V1. The neural gaze modulation is suggested to subserve the conversion from gaze-independent (eye-centered) to dependent (e.g., head-centered) representations. However, it has not been established whether the gaze modulation has significant influences on human visual perception. Here we show that gaze direction modestly but significantly modulates the magnitudes of the motion aftereffect, the tilt aftereffect and the size aftereffect. These aftereffects were stronger when the adaptation and test patterns were presented in the same gaze direction, than when they were presented in different gaze directions, even though the patterns always stimulated the same retinal location. The gaze modulation effect was not statistically significant for the post-adaptation elevation of contrast detection thresholds. The gaze modulation of visual aftereffects provides a useful psychophysical tool to analyze human cortical processes for coordinate transformations of visual space.

Color-selective analysis of luminance-varying stimuli

Alternating adaptation to red and green luminance-varying gratings of different spatial frequencies simultaneously induces opposing color-selective size aftereffects ( Blakemore & Sutton, 1969) in the same retinal locus. With single-color adaptation, the aftereffect is larger and affects test patterns of both colors, though not equally. The color-insensitive portion of the effect shows very substantial interocular and cross-orientation transfer. The color-selective aftereffect, which accounts for about 1/3 of the total effect, is highly selective for both orientation and eye of origin. Thus, both color-selective and color-insensitive mechanisms participate in determining the perceptual characteristics of luminance-varying patterns.

Is the size aftereffect direction selective?

We investigated whether the size aftereffect (apparent spatial-frequency shift after adaptation to slightly different frequencies) is direction selective; i.e., whether it is stronger for test stimuli moving in the adapting direction than the opposite direction. We used drifting sinusoidal gratings of various spatiotemporal frequencies for both adaptation and test stimuli, and the perceived test frequency was estimated by means of a matching technique with a staircase method. For the purpose of comparison, the post-adaptation threshold elevation was measured in addition to the size aftereffect. The results revealed that the direction of stimuli had no influence on the magnitude of the size aftereffect for a wide range of spatiotemporal frequencies, whereas the post-adaptation threshold elevation showed clear direction selectivity. Although there was a significant direction selectivity for the size aftereffect at low spatial and high temporal frequencies, the selectivity was much weaker than that seen in the threshold elevation data. These findings are discussed in relation to the validity of a unified account of selective adaptation at and above threshold contrast and the notion of the separate processing of pattern and motion information.

Contrast adaptation and contrast masking in human vision

After a preliminary study of visual evoked potentials (VEPS) to a test grating seen in the presence of masks at different orientations, psychophysical data are presented showing the effects of adaptation and of masking on thresholds for detecting the same test grating. The test is a vertical grating of spatial frequency 2 cycles per degree; adapting and masking gratings differ from the test either in orientation or in spatial frequency. The effects of adaptation and masking are explained by a single mechanism model that assumes: (i) adaptation and masking both alter the contrast response (or transducer) function of the mechanism that detects the test; (ii) masks, but not adaptors, stimulate the mechanism that detects the test; and (iii) a test is detectable when it raises response level by a constant amount. The model incorporates two distinct tuning functions, a broad adaptive contrast function and a narrow effective contrast function. It accounts adequately for all the data, including the location and size of the facilitative dip found in some masking functions, the constant slopes of the threshold elevation segments of adaptation functions and the varying slopes of masking functions. It also predicts the sometimes surprising joint effects of adaptation followed by masking and of two masks operating simultaneously.

Selective adaptation vs. transfer of decrement: the conjoint effects of neural fatigue and perceptual learning.

Statement of Problem In the last few years, my colleagues and I have been interested in the processes underlying the perceived reversals of reversible figures (Long & Toppino, 1981; Long, Toppino, & Kostenbauder, 1983; Toppino & Long, 1987). One ofthe approaches we have used in our work is the popular selective-adaptation paradigm as a means by which to identify the potential role in this type of illusion of localized neural mechanisms that are subject to fatigue. In this method, an inspection figure is viewed during an adaptation period of perhaps 2-3 min, and a test figure is then shown which shares certain hypothesized features with the adaptation figure. To the extent that the prior adaptation alters the perception of the test figure, one can conclude that similar localized mechanisms are involved in the perception of both figures. This selectiveadaptation paradigm has proven extremely powerful in the investigation of numerous illusions, such as the tilt aftereffect, the motion aftereffect, and the size aftereffect. Reflecting its current popularity, the selective-adaptation paradigm has been referred to as the psychologist's electrode (Frisby, 1980) with which to probe the tuning and response characteristics of hypothesized neural channels in the visual system (e.g., Regan, 1982). In our work, we have attempted to demonstrate the role of localized fatigue effects on the reported reversals of the rotating Necker cube. In this illusion, a threedimensional Necker cube frame is rotated about one of its vertices at a constant speed. An observer viewing either the cube itself or its shadow reports a striking change in the perceived direction of rotation when the cube changes its perspective. As with other reversible figures, the number of reported reversals increases and then levels off at a high rate during a 2-3-min viewing period. For several reasons, we (and others) have proposed that this changing reversal rate reflects fatigue effects in particular visual channels; in our work, we have attempted to demonstrate the limited (i. e., local) character of this fatigue by means of the selective-adaptation paradigm. In one recent experiment (Toppino & Long, 1987, Experiment 1), a rotating cube in the left (or right) visual field was viewed for a 2-min adaptation period, which was followed immediately by a 2-min test period with a cube in the same or

Selective adaptation with reversible figures: don't change that channel.

An adaptation-test paradigm was used in two experiments examining processes underlying the perceived reversals of a rotating Necker cube. Adaptation and test cubes were either the same or different with respect to their visual fields of presentation (Experiment 1) or their sizes (Experiment 2). Results of both experiments indicated that, following subjects’ adaptation to a different cube, reversal rate of the test cube did not differ from that obtained without prior adaptation experience. In contrast, reversal rate of the test cube was elevated following adaptation to the same cube. Additional findings of Experiment 1 were that a test cube presented to the same visual field as the adaptation cube yielded a higher reversal rate than did a simultaneously presented cube in the opposite visual field. Also, the reversal rate of one cube was not influenced by the simultaneous presentation of a second cube. Results of both experiments were interpreted in terms of the fatigue and recovery of multiple, largely independent, localized neural channels. Thus, the results tie reversible-figure illusions to other visual phenomena thought to involve similar fatigue processes within localized visual channels (e.g., tilt, motion, and size aftereffects).