Relative numerosity is constructed from size and density information: Evidence from adaptation.

To dissociate aftereffects of size and density in the perception of relative numerosity, large or small adapter sizes were crossed with high or low adapter densities. A total of 48 participants were included in this preregistered design. To adapt the same retinotopic region as the large adapters, the small adapters were flashed in a sequence so as to "paint" the adapting density across the large region. Perceived numerosities and sizes in the adapted region were then compared to those in an unadapted region in separate blocks of trials, so that changes in density could be inferred. These density changes were found to be bidirectional and roughly symmetric, whereas the aftereffects of size and number were not symmetric. A simple account of these findings is that local adaptations to retinotopic density as well as global adaptations to size combine in producing numerosity aftereffects measured by assessing perceived relative number. Accounts based on number adaptation are contraindicated, in particular, by the result of adapting to a large, sparse adapter and testing with a stimulus with a double the density but half number of dots.

Aftereffects of visuomanual prism adaptation in auditory modality: Review and perspectives.

Visuomanual prism adaptation (PA), which consists of pointing to visual targets while wearing prisms that shift the visual field, is one of the oldest experimental paradigms used to investigate sensorimotor plasticity. Since the 2000's, a growing scientific interest emerged for the expansion of PA to cognitive functions in several sensory modalities. The present work focused on the aftereffects of PA within the auditory modality. Recent studies showed changes in mental representation of auditory frequencies and a shift of divided auditory attention following PA. Moreover, one study demonstrated benefits of PA in a patient suffering from tinnitus. According to these results, we tried to shed light on the following question: How could this be possible to modulate audition by inducing sensorimotor plasticity with glasses? Based on the literature, we suggest a bottom-up attentional mechanism involving cerebellar, parietal, and temporal structures to explain crossmodal aftereffects of PA. This review opens promising new avenues of research about aftereffects of PA in audition and its implication in the therapeutic field of auditory troubles.

Religious labels and food preferences, but not country of origin, support opposing face aftereffects.

Face templates can be experimentally manipulated, and category-contingent aftereffects suggest discrete templates across social groups. We tested whether 1) explicit religious labels, 2) food preferences, and 3) country of origin would support religion-contingent aftereffects across Christians and Muslims face sets. While viewing face images, ninety-three participants heard audio that stated either 1) a character's religious identity, 2) preferred food, or 3) country of origin. Participants viewed contracted Christian faces and expanded Muslim faces during the training phase. To measure adaptation, before and after the training phases, participants selected the face out of a pair of expanded and contracted Christian or Muslim faces that they found more attractive. Contingent aftereffects were found in the religious explicit (t(30) = 2.49, p = 0.02, Cohen's d = 0.58) and food conditions (t(30) = -3.77, p < 0.01, Cohen's d = -0.82), but not the country condition (t(30) = 1.64, p = 0.11, Cohen's d = 0.31). This suggests that religious labels and food preferences create socially meaningful groups, but country of origin does not. This is evidence of an impact of social categorization on visual processing.

Inattentional aftereffects: The role of attention on the strength of the motion aftereffect.

The way that attention affects the processing of visual information is one of the most intriguing fields in the study of visual perception. One way to examine this interaction is by studying the way perceptual aftereffects are modulated by attention. In the present study, we have manipulated attention during adaptation to translational motion generated by coherently moving random dots, in order to investigate the effect of the distraction of attention on the strength of the peripheral dynamic motion aftereffect (MAE). A foveal rapid serial visual presentation task (RSVP) of varying difficulty was introduced during the adaptation period while the adaptation and test stimuli were presented peripherally. Furthermore, to examine the interaction between the physical characteristics of the stimulus and attention, we have manipulated the motion coherence level of the adaptation stimuli. Our results suggested that the removal of attention through an irrelevant task modulated the MAE's magnitude moderately and that such an effect depends on the stimulus strength. We also showed that the MAE still persists with subthreshold and unattended stimuli, suggesting that perhaps attention is not required for the complete development of the MAE.

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.

Stronger tilt aftereffects in persons with schizophrenia.

Individuals with schizophrenia may fail to appropriately use temporal context and apply past environmental regularities to the interpretation of incoming sensory information. Here we use the visual system as a test bed for investigating how prior experience shapes perception in individuals with schizophrenia. Specifically, we use visual aftereffects, illusory percepts resulting from prior exposure to visual input, to measure the influence of prior events on current processing. At a neural level, visual aftereffects arise due to attenuation in the responses of neurons that code the features of the prior stimulus (neuronal adaptation) and subsequent disinhibition of neurons signaling activity at the opposite end of the feature dimension. In the current study, we measured tilt aftereffects and negative afterimages, 2 types of aftereffects that reflect, respectively, adaptation of cortical orientation-coding neurons and adaptation of subcortical and retinal luminance-coding cells in persons with schizophrenia (PSZ; n = 36) and demographically matched healthy controls (HC; n = 22). We observed stronger tilt aftereffects in PSZ compared to HC, but no difference in negative afterimages. Stronger tilt aftereffects were related to more severe negative symptoms. These data suggest oversensitivity to recent regularities, in the form of stronger visual adaptation, at cortical, but not subcortical, levels in schizophrenia. (PsycInfo Database Record (c) 2021 APA, all rights reserved).

Motion-form interaction: Motion and form aftereffects induced by distorted static natural scenes.

Spatially varying distortions (SVDs) are common artifacts of spectacles like progressive additional lenses (PALs). To habituate to distortions of PALs, the visual system has to adapt to distortion-induced image alterations, termed skew adaptation. But how this visual adjustment is achieved is largely unknown. This study examines the properties of visual adaptation to distortions of PALs in natural scenes. The visual adaptation in response to altered form and motion features of the natural stimuli were probed in two different psychophysical experiments. Observers were exposed to distortions in natural images, and form and motion aftereffects were tested subsequently in a constant stimuli procedure where subjects were asked to judge the skew, or the motion direction of an according test stimulus. Exposure to skewed natural stimuli induced a shift in perceived undistorted form as well as motion direction, when viewing distorted dynamic natural scenes, and also after exposure to static distorted natural images. Therefore, skew adaptation occurred in form and motion for dynamic visual scenes as well as static images. Thus, specifically in the condition of static skewed images and the test feature of motion direction, cortical interactions between motion-form processing presumably contributed to the adaptation process. In a nutshell, interfeature cortical interactions constituted the adaptation process to distortion of PALs. Thus, comprehensive investigation of adaptation to distortions of PALs would benefit from taking into account content richness of the stimuli to be used, like natural images.

Invisible Adaptation: The Effect of Awareness on the Strength of the Motion Aftereffect.

The ability to process information despite the lack of perceptual awareness is one of the most fascinating aspects of the visual system. Such unconscious processing is often investigated using adaptation, where any presence of the former can be traced by its footprint on aftereffects following the latter. We have investigated the mechanisms of the motion aftereffect (MAE) using random dot displays of varying motion coherence as well as crowding to modulate both the physical as well as the perceptual strength of the adaptation stimulus. Perceptual strength was quantitatively measured as the performance in a forced-choice direction-discrimination task. A motion-nulling technique was used to quantitatively measure the strength of the MAE. We show that the strength of the dynamic MAE is independently influenced by both the physical stimulus strength as well as the subjective perceptual strength, with the effect of the former being more prominent than that of the latter. We further show that the MAE still persists under conditions of subthreshold perception. Our results suggest that perceptual awareness can influence the strength of visual processing, but the latter is not fully dependent on the former and can still take place at its partial or even total absence.

Control of visual adaptation depends upon task.

The visual system optimizes its functioning for a given environment through processes collectively called adaptation. It is currently unknown, however, whether adaptation is affected by the particular task the observer performs within that environment. Two experiments tested whether this is the case. Observers adapted to high contrast grating patterns, and the decay of adaptation was measured using a version of the tilt-aftereffect, while they performed two different secondary tasks. One task involved judging the luminance of a small circular spot at fixation, and was expected to be unaffected by adaptation. The other secondary task involved judging a low contrast grating, and adaptation was expected to make this task difficult by reducing the visibility of the grating. Identical displays containing both a fixation spot and a grating were used for both tasks. Tilt-aftereffects were smaller when subjects concurrently performed the grating task than when they performed the fixation task. These results suggest that the control of adaptation, in this case its decay, is sensitive to the nature of the task the observer is performing. Adaptation may attempt to optimize vision with respect to many different criteria simultaneously; task is likely one of the criteria included in this process.

Adaptation to mean and variance: Interrelationships between mean and variance representations in orientation perception.

When there are many visual items, the visual system could represent their summary statistics (e.g., mean, variance) to process them efficiently. Although many previous studies have investigated the mean or variance representation itself, a relationship between these two ensemble representations has not been investigated much. In this study, we tested the potential interaction between mean and variance representations by using a visual adaptation method. We reasoned that if mean and variance representations interact with each other, an adaptation aftereffect to either mean or variance would influence the perception of the other. Participants watched a sequence of orientation arrays containing a specific statistical property during the adaptation period. To produce an adaptation aftereffect specific to variance or mean, one property of the adaptor arrays (variance or mean) had a fixed value while the other property was randomly varied. After the adaptation, participants were asked to discriminate the property of the test array that was randomly varied during the adaptation. We found that the adaptation aftereffect of orientation variance influenced the sensitivity of mean orientation discrimination (Experiment 1), and that the adaptation aftereffect of mean orientation influenced the bias of orientation variance discrimination (Experiment 2). These results suggest that mean and variance representations do closely interact with each other. Considering that mean and variance reflect the representative value and dispersion of multiple items respectively, the interactions between mean and variance representations may reflect their complementary roles to summarize complex visual information effectively.

Individual movement features during prism adaptation correlate with after-effects and interlimb transfer.

The human nervous system displays such plasticity that we can adapt our motor behavior to various changes in environmental or body properties. However, how sensorimotor adaptation generalizes to new situations and new effectors, and which factors influence the underlying mechanisms, remains unclear. Here we tested the general hypothesis that differences across participants can be exploited to uncover what drives interlimb transfer. Twenty healthy adults adapted to prismatic glasses while reaching to visual targets with their dominant arm. Classic adaptation and generalization across movement directions were observed but transfer to the non-dominant arm was not significant and inter-individual differences were substantial. Interlimb transfer resulted for some participants in a directional shift of non-dominant arm movements that was consistent with an encoding of visuomotor adaptation in extrinsic coordinates. For some other participants, transfer was consistent with an intrinsic coordinate system. Simple and multiple regression analyses showed that a few kinematic parameters such as peak acceleration (or peak velocity) and variability of movement direction were correlated with interlimb transfer. Low peak acceleration and low variability were related to extrinsic transfer, while high peak acceleration and high variability were related to intrinsic transfer. Motor variability was also positively correlated with the magnitude of the after-effect systematically observed on the dominant arm. Overall, these findings on unconstrained movements support the idea that individual movement features could be linked to the sensorimotor adaptation and its generalization. The study also suggests that distinct movement characteristics may be related to different coordinate frames of action representations in the nervous system.

Rotating One's Head Modulates the Perceived Velocity of Motion Aftereffect.

As a prominent illusion, the motion aftereffect (MAE) has traditionally been considered a visual phenomenon. Recent neuroimaging work has revealed increased activities in MT+ and decreased activities in vestibular regions during the MAE, supporting the notion of visual-vestibular interaction on the MAE. Since the head had to remain stationary in fMRI experiments, vestibular self-motion signals were absent in those studies. Accordingly, more direct evidence is still lacking in terms of whether and how vestibular signals modulate the MAE. By developing a virtual reality approach, the present study for the first time demonstrates that horizontal head rotation affects the perceived velocity of the MAE. We found that the MAE was predominantly perceived as moving faster when its direction was opposite to the direction of head rotation than when its direction was the same as head rotation. The magnitude of this effect was positively correlated with the velocity of head rotation. Similar result patterns were not observed for the real motion stimuli. Our findings support a 'cross-modal bias' hypothesis that after living in a multisensory environment long-term the brain develops a strong association between signals from the visual and vestibular pathways. Consequently, weak biasing visual signals in the associated direction can spontaneously emerge with the input of vestibular signals in the multisensory brain areas, substantially modulating the illusory visual motion represented in those areas as well. The hypothesis can also be used to explain other multisensory integration phenomena.

Brief facial emotion aftereffect occurs earlier for angry than happy adaptation.

Prolonged exposure to an emotional face biases our judgement of subsequent face stimulus toward the opposite emotion. This emotion aftereffect has been suggested to occur as early as 35 ms exposure duration in cartoon faces. In the current study, we are interested in investigating the time-course of brief emotional face adaptation, and the relationship between brief emotional face adaptation and prolonged emotional face adaptation. We adapted the subjects from 17 ms to 1000 ms with a happy or angry adapting face. We found that a facial emotion adaptation aftereffect started from 17 ms adapting duration for angry face adaptation, and from 50 ms for happy face adaptation. Factor analysis on the adaptation effects highlighted three different components: brief angry adaptation (17 ms, 34 ms, and 50 ms), prolonged angry adaptation (100 ms and 1000 ms), and happy face adaptation (from 17 ms to 1000 ms). We found that the brief angry face adaptation was negatively associated with the awareness of the adapting face, and the prolonged angry face adaptation was stronger in subjects who perceived the angry adapting face as more negative in valence. Together, these findings suggest that (1) facial emotion adaptation can be induced by brief (17 ms) adapting face presentation; (2) brief angry face adaptation may be related to early visual processing, whereas prolonged angry face adaptation may be related to adaptation at later and higher-level visual emotional processing; and (3) brief and prolonged adaptations may adapt different neural populations. Our findings thus shed light on the current understanding of the neural mechanisms of emotional face adaptation.

Simulated prism exposure in immersed virtual reality produces larger prismatic after-effects than standard prism exposure in healthy subjects.

Previous studies have shown that the size of the leftward bias after exposure to rightward prism-deviation (the prismatic after-effect) depends on the degree of rightward prism-deviation as well as the type of visual feedback receives during exposure to prism-deviation. In this study, we tested if it was possible to obtain a leftward bias in pointing precision using two different methods of creating diverted visual input by simulating a rightward prism diversion of visual input in immersive virtual reality. We compared the results to the leftward bias in pointing precision obtained after exposure to standard prism goggles deviating visual input 10 degrees to the right. Twenty healthy participants were subjected to one session of standard prism adaptation therapy under three different conditions of deviated visual input: 1) created by imitating a 10 degree leftward rotation of the head (VRR), 2) created by imitating a 2D leftward horizontal displacement of 10 degrees (VRS) and 3) a control condition using real right-deviating prisms (PCP). The study showed that the simulated prisms in the VRR and VRS conditions produced deviations in pointing precision of a similar size. However, exposure to the VRS and VRR conditions both produced larger prismatic after-effects than the exposure to real prism goggles. This research is important for the development and use of virtual reality systems in the rehabilitation of neglect after brain injury as it emphasizes that the adjustment to deviated visual input may be affected positively by the use of immersive virtual reality technology.

Limited Attention Diminishes Spatial Suppression From Large Field Glass Patterns.

Glass patterns (GPs) consist of randomly distributed dot pairs (dipoles) whose orientations are determined by specific geometric transforms. We investigated the role of visuospatial attention in the processing of global form from GPs by measuring the effect of distraction on adaptation to GPs. In the nondistracted condition, observers were adapted to coherent GPs. After the adaptation period, they were presented with a test GP divided in two halves along the vertical and were required to judge which side of the test GP was more coherent. In the attention-distracted condition, a high-load rapid serial visual presentation task was performed during the adapting period. The magnitude of the form after-effect was measured using a technique that measures the coherence level at which the test GP appears random. The rationale was that if attention has a modulatory effect on the spatial summation of dipoles, in the attention-distracted condition, we should expect a weaker form after-effect. However, the results showed stronger form after-effect in the attention-distracted condition than in the nondistracted condition, suggesting that distraction during adaptation increases the strength of form adaptation. Additional experiments suggested that distraction may reduce the spatial suppression from large-scale textures, strengthening the spatial summation of local-oriented signals.

The effect of perceptual contour orientation uncertainty on the tilt aftereffect.

The tilt aftereffect (TAE) occurs when, after adapting to an oriented line, a vertical line appears to be tilted in the opposite direction. The magnitude of the TAE has been shown to relate to the salience of the adapting stimulus (e.g., its contrast) as well as to the similarity between the adapting and testing stimuli. However, the relationship between TAE and orientation uncertainty - variability in the perceived orientation of the stimulus - of either the adapting or the testing stimulus and, more importantly, change in orientation uncertainty as a function of adaptation have not previously been explored. We manipulated stimulus salience by using a variety of contour types, including real and illusory contours. Tilt aftereffects were observed even for stimuli that had much weaker or invisible illusory contours. Orientation uncertainty of the adapting stimulus, as measured by the slope of a psychometric function in orientation discrimination, was positively correlated with TAE magnitude for real and illusory contours, but not for stimuli with weak contour percepts. On an individual subject level, orientation uncertainty increased post-adaptation and was correlated with pre-adaptation uncertainty. That is, individuals with more variability in their perception of orientation before adaptation showed increased variability in orientation discrimination following adaptation. This may account for some of the variability in TAE across individuals and stimulus types and is consistent with previous findings on increased orientation discrimination thresholds post-adaptation for nearby orientations.

Meta-analysis of the visuospatial aftereffects of prism adaptation, with two novel experiments.

We present a meta-analysis of the effects of visuomotor adaptation to leftward displacing prisms on visuospatial judgements in healthy people, as assessed by perceptual (landmark) and manual versions of the line bisection task. To supplement previously published datasets, we report two novel experiments: Experiment 1 (n = 12) found null effects of adaptation to 10° leftward prisms on spatial bias in the landmark task, and Experiment 2 (n = 24) found null effects of 12° leftward prisms on spatial bias in a computerised line bisection task. Including these data, we considered 17 experiments for the landmark task (total n = 256), and 12 experiments for line bisection (total n = 172), in which participants were adapted for between 7 and 20 min to prism strengths from 8 to 17°. A random-effects meta-analysis, with prism strength and exposure duration as moderators, confirmed robust rightward shifts in visuospatial judgements following leftward prism adaptation. The average standardised effect sizes (Cohen's d) were similar between tasks, increasing by around .1 per degree of prismatic displacement, and being boosted by a long (10 min +) period of prism exposure. However, the quality of evidence and precision of prediction was superior for the landmark task, with a higher signal-to-noise ratio within studies, and less heterogeneity between studies. We suggest that line bisection responses may be contaminated by sensorimotor aftereffects, and that the landmark task is a more suitable method for measuring true visuospatial aftereffects of prism adaptation. To harness these effects, we recommend that researchers should expose participants to 15° (or higher) leftward prisms for more than ten minutes, with upwards of 250 pointing movements. Power calculations should take account of heterogeneity in the true effect size between studies; and further investigation of the factors underlying this heterogeneity will help to refine optimally-effective methods.

The contribution of local and global motion adaptation in the repulsive direction aftereffect.

After adapting to a certain motion direction, our perception of a similar direction will be repelled away from the adapting direction, a phenomenon known as the direction aftereffect (DAE). As the motion system consists of local and global processing stages, it remains unclear how the adaptation of the two stages contributes in producing the DAE. The present study addresses this question by independently inducing adaptation at local and global motion-processing levels. Local adaptation was manipulated by presenting test stimuli at either adapted or nonadapted locations. Global adaptation was manipulated by embedding one or five global motion directions in the adapting motion. Repulsive DAE, when measured using a multiple-element test pattern, was stronger when it was produced by global adaptation than when produced by local adaptation. Specifically, the DAE resulting from local adaptation (a) decreased when test orientations differed from adapting orientation, (b) decreased when local directions were disambiguated using plaid stimuli, (c) remained the same even when attention was focused at specific test locations during adaptation, and (d) increased when tested with a single element. Overall, these findings suggest that the strength of repulsive DAE depends on both the motion-processing level at which adaptation occurs and the level at which the DAE was tested. Furthermore, the repulsive DAE arising from local adaptation alone can be explained by the propagation of local speed repulsion instead of local direction repulsion. Findings are discussed in the context of how motion aftereffects arise from the adaptation of a hierarchical motion system.

Bidirectional aftereffects in perceived contrast.

It is well known that prolonged observation of a high-contrast stimulus alters the perception of a subsequent test stimulus. Previous studies of perceived contrast shifts only reported perceived contrast reductions. Here, we used successive presentations of test and reference stimuli and found that perceived contrast was reduced if tests had a lower contrast than adaptors but was significantly enhanced when tests had a higher contrast than adaptors. Such bidirectional contrast aftereffects were not observed for single adaptor flashes but became increasingly pronounced for repeated adaptor presentations, thereby suggesting that the aftereffect is a consequence of adaptation rather than of attentional cuing or temporal repulsion. In addition, perceived contrast reduction weakened as we increasingly jittered the spatial position of the adaptor, but perceived contrast enhancement was observed for large spatial range of jittered adaptor positions. We conclude that aftereffects involve adaptation in distinct mechanisms with narrow and broad spatial tunings. Results suggest that the visual system not only possesses low-level contrast encoding units, which monotonically increase their responses as physical contrast increases, but is also equipped with high-level channels selectively tuned for particular contrast ranges.

Everything is illuminated: Prismatic adaptation lowers visual detection threshold in normal subjects.

Prismatic adaptation (PA) results from repeated ballistic movements of the dominant arm toward visual targets while wearing prisms shifting the visual field laterally (visuomotor prismatic training [VPT]). Following PA, subjects' pointing movements are deviated contralaterally to prismatic shift (aftereffect). The question of whether spatial attention is also biased in the same direction remains controversial in the scientific literature. To investigate the effect of PA on spatial attention, we asked healthy participants to perform a visual detection threshold task before and after VPT with left- and right-deviating prisms and visuomotor training without prisms. Our results demonstrate that both left and right VPTs modulate visual detection threshold, significantly ameliorating detection accuracy and response times bilaterally. These data indicate that PA modulates visual attention bilaterally and that detection threshold paradigms are sensitive to its effects in the visual domain. We suggest that the described PA effects are mediated by the joint action of attentional and alerting mechanisms. (PsycINFO Database Record (c) 2018 APA, all rights reserved).