No effect of spatial congruence on rapid temporal recalibration to audiovisual asynchrony.

The brain integrates multisensory information to construct coherent perceptual representations based on spatial and temporal congruence. Intriguingly, multisensory timing perception can be flexibly calibrated. Repeated exposure to audiovisual asynchrony induces shifts in subjective simultaneity (temporal recalibration). Spatial congruence is known to serve as a grouping cue for recalibration when the audiovisual temporal relationship is ambiguous during exposure. A single exposure to audiovisual asynchrony can also trigger temporal recalibration (rapid recalibration). However, it has been suggested that the underlying mechanisms of these temporal recalibrations differ. Here, we examined whether spatial congruence can be a grouping cue for rapid recalibration when audiovisual pairs are not defined by temporal relationships. Participants made a simultaneity judgment for a pair of audiovisual stimuli after adapting three consecutive stimuli once in a "light-sound-light" or "sound-light-sound" order with an equal temporal interval. The spatial positions of the adapting stimuli were manipulated as an audiovisual pair from the same position (e.g., left) and the remaining stimulus from another position (e.g., right). In three experiments, the spatial congruence of the audiovisual adapting stimuli did not show a modulatory effect, while we replicated the rapid recalibration effects. Rather, rapid recalibration occurred according to the temporal order of the first light and sound. Our findings suggest that, in contrast to temporal recalibration with repeated exposure, the perceptual systems underlying rapid recalibration simply combine individual visual and auditory inputs based on the order in which they arrive.

No relationships between frequencies of mind-wandering and perceptual rivalry.

Our minds frequently wander from a task at hand. This mind-wandering reflects fluctuations in our cognitive states. The phenomenon of perceptual rivalry, in which one of the mutually exclusive percepts automatically switches to an ambiguous sensory input, is also known as fluctuations in our perceptual states. There may be possible relationships between the mind-wandering and perceptual rivalry, given that physiological responses such as fluctuations in pupil diameter, which is an index of attentional/arousal states, are related to the occurrence of both phenomena. Here, we investigate possible relationships between mind-wandering and perceptual rivalry by combining experimental and questionnaire methods in an online research protocol. In Study 1, we found no statistically significant relationships between subjective mind-wandering tendencies measured by questionnaires and frequencies of perceptual rivalry for Necker-cube or structure-from-motion stimuli. Study 2 replicated the results of Study 1 and further confirmed no statistically significant relationships between behavioral measurements of mind-wandering tendencies estimated by sustained attention to response task and frequencies of perceptual rivalry. These findings suggest that mind-wandering and perceptual rivalry would be based on different mechanisms, possibly higher-level cognitive and lower-level perceptual ones.

No differences in implicit hand maps among different degrees of autistic traits.

People with autism spectrum disorder (ASD) or higher levels of autistic traits have atypical characteristics in sensory processing. Atypicalities have been reported for proprioceptive judgments, which are tightly related to internal bodily representations underlying position sense. However, no research has directly investigated whether self-bodily representations are different in individuals with ASD. Implicit hand maps, estimated based on participants' proprioceptive sensations without sight of their hand, are known to be distorted such that the shape is stretched along the medio-lateral hand axis even for neurotypical participants. Here, with the view of ASD as falling on a continuous distribution among the general population, we explored differences in implicit body representations along with autistic traits by focusing on relationships between autistic traits and the magnitudes of the distortions in implicit hand maps (N ~ 100). We estimated the magnitudes of distortions in implicit hand maps both for fingers and hand surfaces on the dorsal and palmar sides of the hand. Autistic traits were measured by questionnaires (Autism Spectrum [AQ] and Empathy/Systemizing [EQ-SQ] Quotients). The distortions in implicit hand maps were replicated in our experimental situations. However, there were no significant relationships between autistic traits and the magnitudes of the distortions as well as within-individual variabilities in the maps and localization performances. Consistent results were observed from comparisons between IQ-matched samples of people with and without a diagnosis of ASD. Our findings suggest that there exist perceptual and neural processes for implicit body representations underlying position sense consistent across levels of autistic traits.

Exploring relationships between autistic traits and body temperature, circadian rhythms, and age.

The number of clinical diagnoses of autism spectrum disorder (ASD) is increasing annually. Interestingly, the human body temperature has also been reported to gradually decrease over the decades. An imbalance in the activation of the excitatory and inhibitory neurons is assumed to be involved in the pathogenesis of ASD. Neurophysiological evidence showed that brain activity decreases as cortical temperature increases, suggesting that an increase in brain temperature enhances the inhibitory neural mechanisms. Behavioral characteristics specific to clinical ASD were observed to be moderated when people with the diagnoses had a fever. To explore the possible relationship between ASD and body temperature in the general population, we conducted a survey study using a large population-based sample (N ~ 2000, in the age groups 20s to 70s). Through two surveys, multiple regression analyses did not show significant relationships between axillary temperatures and autistic traits measured by questionnaires (Autism Spectrum (AQ) and Empathy/Systemizing Quotients), controlling for covariates of age and self-reported circadian rhythms. Conversely, we consistently observed a negative relationship between AQ and age. People with higher AQ scores tended to have stronger eveningness. Our findings contribute to the understanding of age-related malleability and the irregularity of circadian rhythms related to autistic traits.

Tilt adaptation aftereffects reveal fundamental perceptual characteristics of tactile orientation processing on the hand.

Orientation information contributes substantially to our tactile perception, such as feeling an object's shape on the skin. For vision, a perceptual adaptation aftereffect (tilt aftereffect; TAE), which is well explained by neural orientation selectivity, has been used to reveal fundamental perceptual properties of orientation processing. Neural orientation selectivity has been reported in somatosensory cortices. However, little research has investigated the perceptual characteristics of the tactile TAE. The aim of the current study was to provide the first demonstration of a tactile TAE on the hand and investigate the perceptual nature of tactile TAE on the hand surface. We used a 2-point stimulation with minimal input for orientation. We found clear TAEs on the hand surface: Adaptation induced shifts in subjective vertical sensation toward the orientation opposite to the adapted orientation. Further, adaptation aftereffects were purely based on orientation processing given that the effects transferred between different lengths across adaptor and test stimuli and type of stimuli. Finally, adaptation aftereffects were anchored to the hand: tactile TAE occurred independently of hand rotation and transferred from palm to dorsum sides of the hand, while the effects did not transfer between hands. Our findings demonstrate the existence of hand-centered perceptual processing for basic tactile orientation information. (PsycInfo Database Record (c) 2022 APA, all rights reserved).

Noninformative Vision of Body Movements can Enhance Tactile Discrimination.

Vision of the body without task cues enhances tactile discrimination performance. This effect has been investigated only with static visual information, although our body usually moves, and dynamic visual and bodily information provides ownership (SoO) and agency (SoA) sensations to body parts. We investigated whether vision of body movements could enhance tactile discrimination performance. Participants observed white dots without any textural information showing lateral hand movements (dynamic condition) or static hands (static condition). For participants experiencing the dynamic condition first, it induced a lower tactile discrimination threshold, as well as a stronger SoO and SoA, compared to the static condition. For participants observing the static condition first, the magnitudes of the enhancement effect in the dynamic condition were positively correlated between the tactile discrimination and SoO/SoA. The enhancement of the dynamic visual information was not observed when the hand shape was not maintained in the scrambled white dot images. Our results suggest that dynamic visual information without task cues can enhance tactile discrimination performance by feeling SoO and SoA only when it maintains bodily information.

Bodily ownership and agency sensations in a natural state.

Our bodily sensation is a fundamental cue for our self-consciousness. Whereas experimental studies have uncovered characteristics of bodily sensation, these studies investigated bodily sensations through manipulating bodily sensations to be apart from one's own body and to be assigned to external, body-like objects. In order to capture our bodily sensation as it is, this questionnaire survey study explored the characteristics of bodily sensation using a large population-based sample (N = 580, comprising 20s to 70s age groups) without experimental manipulations. We focused on the sensations of ownership, the feeling of having a body part as one's own, and agency, the feeling of controlling a body part by oneself, in multiple body parts (the eyes, ears, hands, legs, nose, and mouth). The ownership and agency sensations were positively related to each other in each body part. Interestingly, the agency sensation of the hands and legs had a positive relationship with the ownership sensations of the other body parts. We also found the 60s age group had a unique internal configuration, assessed by the similarity of rating scores, of the body parts for each bodily sensation. Our findings revealed the existence of unique characteristics for bodily sensations in a natural state.

Tactile interactions in the path of tactile apparent motion.

Perceptual completion is a fundamental perceptual function serving to maintain robust perception against noise. For example, we can perceive a vivid experience of motion even for the discrete inputs across time and space (apparent motion: AM). In vision, stimuli irrelevant to AM perception are suppressed to maintain smooth AM perception along the AM trajectory where no physical inputs are applied. We investigated whether such perceptual masking induced by perceptual completion of dynamic inputs is general across sensory modalities by focusing on touch. Participants tried to detect a vibro-tactile target stimulus presented along the trajectory of AM induced by two other tactile stimuli on the forearm. In a control condition, the inducing stimuli were applied simultaneously, resulting in no motion percept. Tactile target detection was impaired with tactile AM. Our findings support the notion that the perceptual masking induced by perceptual completion mechanism of AM is a general function rather than a sensory specific effect.

Visual motion information modulates tactile roughness perception.

We perceive the roughness of an object through our eyes and hands. Many crossmodal studies have reported that there is no clear visuo-tactile interaction in roughness perception using static visual cues. One exception is that the visual observation of task-irrelevant hand movements, not the texture of task-relevant objects, can enhance the performance of tactile roughness discrimination. Our study investigated whether task-irrelevant visual motion without either object roughness or bodily cues can influence tactile roughness perception. Participants were asked to touch abrasive papers while moving their hand laterally and viewing moving or static sine wave gratings without being able to see their hand, and to estimate the roughness magnitude of the tactile stimuli. Moving gratings with a low spatial frequency induced smoother roughness perceptions than static visual stimuli when the visual grating moved in the direction opposite the hand movements. The effects of visual motion did not appear when the visual stimuli had a high spatial frequency or when the participants touched the tactile stimuli passively. These results indicate that simple task-irrelevant visual movement without object roughness or bodily cues can modulate tactile roughness perception with active body movements in a spatial-frequency-selective manner.

Tactile distance adaptation aftereffects do not transfer to perceptual hand maps.

Recent studies have demonstrated that mental representations of the hand dorsum are distorted even for healthy participants. Perceptual hand maps estimated by pointing to specific landmarks (e.g., knuckles and tips of fingers) is stretched and shrunk along the medio-lateral and the proximo-distal axes, respectively. Similarly, tactile distance perception between two touches is longer along the medio-lateral axis than the proximo-distal axis. The congruency of the two types of distortions suggests that common perceptual and neural representations may be involved in these processes. Prolonged stimulation by two simultaneous touches having a particular distance can bias subsequent perception of tactile distances (e.g., adaptation to a long distance induces shorter stimuli to be perceived even shorter). This tactile distance adaptation aftereffect has been suggested to occur based on the modulations of perceptual and neural responses at low somatosensory processing stages. The current study investigated whether tactile distance adaptation aftereffects affect also the pattern of distortions on the perceptual hand maps. Participants localized locations on the hand dorsum cued by tactile stimulations (Experiment 1) or visually presented landmarks on a hand silhouette (Experiment 2). Each trial was preceded by adaptation to either a small (2 cm) or large (4 cm) tactile distance. We found clear tactile distance aftereffects. However, no changes were observed for the distorted pattern of the perceptual hand maps following adaptation to a tactile distance. Our results showed that internal body representations involved in perceptual distortions may be distinct between tactile distance perception and the perceptual hand maps underlying position sense.

Anisotropy in tactile time perception.

Spatial distortions in touch have been investigated since the 19th century. For example, two touches applied to the hand dorsum feel farther apart when aligned with the mediolateral axis (i.e., across the hand) than when aligned with the proximodistal axis (along the hand). Stimulations to our sensory receptors are usually dynamic, where spatial and temporal inputs closely interact to establish our percept. For example, physically bigger tactile stimuli are judged to last longer than smaller stimuli. Given such links between space and time in touch, we investigated whether there is a tactile anisotropy in temporal perception analogous to the anisotropy described above. In this case, the perceived duration between the onset of two touches should be larger when they are aligned with the mediolateral than with the proximodistal axis of the hand dorsum. To test this hypothesis, we asked participants to judge which of two tactile temporal sequences, having the same spatial separation along and across the dorsum, felt longer. A clear anisotropy of the temporal perception was observed: temporal intervals across the hand were perceived as longer than those along the hand. Consistent with the spatial anisotropy, the temporal anisotropy did not appear on the palm side of the hand, indicating that the temporal anisotropy was based on perceptual processes rather than top-down modulations such as attentional or decisional/response biases. Contrary to our predictions, however, we found no correlation between the magnitudes of the temporal and spatial anisotropies. Our results demonstrated a novel type of temporal illusion in touch, which is strikingly similar in nature to the previously reported spatial anisotropy. Thus, qualitatively similar distorted somatosensory representations appear to underlie both temporal and spatial processing of touch.

Autistic Communication and Imagination Sub-Traits Are Related to Audiovisual Temporal Integration in the Stream-Bounce Illusion.

Autism spectrum disorder (ASD) is characterized by atypical social communication and restricted and repetitive behaviors; such traits are continuously distributed across nonclinical and clinical populations. Recently, relationships between ASD traits and low-level multisensory processing have been investigated, because atypical sensory reactivity has been regarded as a diagnostic criterion of ASD. Studies regarding an audiovisual illusion (the double-flash illusion) reported that social communication difficulties are related to temporal aspects of audiovisual integration. This study investigated whether similar relationships exist in another audiovisual illusion (the stream-bounce effect). In this illusion, two visual objects move toward each other, coincide, and pass each other, and the presentation of a transient sound at their coincidence induces a dominant perception that they bounce away from each other. Typically developing adults were recruited to perform experimental trials involving the stream-bounce effect. We measured their ASD traits using the Autism-Spectrum Quotient. The total quotient score was not related to any behavioral measurements of the effect. In contrast, for participants with higher difficulty in communication, the greatest magnitude of the stream-bounce effect occurred when the presentation timing of the sound tended to follow the visual coincidence. Participants with higher difficulty in imagination also showed the greatest magnitude of the effect when the presentation timing of the sound preceded that of the visual coincidence. Our findings regarding the stream-bounce effect, along with previous findings regarding the double-flash illusion, suggest that atypical temporal audiovisual integration is uniquely related to ASD sub-traits, especially in social communication.

Effects of spatial consistency and individual difference on touch-induced visual suppression effect.

Crossmodal studies have reported not only facilitatory but also inhibitory perceptual interactions. For instance, tactile stimulation to the index finger of a hand leads to the degradation of visual discrimination performance (touch-induced visual suppression, TIVS). It has been suggested that the magnitude of TIVS depends on the spatial congruency of visuo-tactile stimuli and on individual differences in task performance. We performed a detailed investigation of the effects of spatial consistency and individual differences on the occurrence of TIVS. The visual target and tactile stimulus were presented at co-localized, ipsilateral but not co-localized, or contralateral positions. The degree of autistic traits has been reported to be well variable among the general population and to reflect differences in sensory processing. Therefore, we assessed the magnitude of autistic traits using the autism-spectrum quotient (AQ) as an index of individual differences. TIVS occurred particularly at the ipsilateral but not co-localized position. In contrast, the magnitude of the TIVS was positively correlated with the AQ score when the stimuli were presented at the co-localized position. These findings suggest that the occurrence of TIVS can be modulated both by the spatial relationship between the visual and tactile stimuli and by individual differences in autistic traits.

Investigating the Effects of Tactile Masking and Surface Texture on the Velvet Hand Illusion.

When we hold thin metallic bars between the palms of our hands and rub the palms against each other, the feeling of touching smooth velvet occurs. Previous studies have shown that tactile motion and pressure on the palms are important for this velvet hand illusion. Interestingly, when we experience this illusion, we cannot feel the texture of our palms as we usually do. In the present study, we investigated the possibility that tactile masking contributes to the occurrence of the velvet hand illusion. We measured vibrotactile detection performance on the palms of the hands during the occurrence of the velvet hand illusion. The detection performance was worse when the illusion occurred than when it did not. Moreover, the degradation of the detection performance correlated positively with the subjective magnitude of the illusion. We also examined whether additional surface texture could affect the occurrence of the illusion and found that the illusion became weaker as the roughness of the surface increased. These findings suggest that tactile motion and pressure information delivered by the bars of smooth surface mask tactile sensations on the palms of the hands, resulting in an illusory smooth, frictionless feeling on the palms.

Visual percepts modify iconic memory in humans.

Our visual system briefly retains a trace of a stimulus after it disappears. This phenomenon is known as iconic memory and its contents are thought to be temporally integrated with subsequent visual inputs to produce a single composite representation. However, there is little consensus on the temporal integration between iconic memory and subsequent visual inputs. Here, we show that iconic memory revises its contents depending upon the configuration of the newly produced single representation with particular temporal characteristics. The Poggendorff illusion, in which two collinear line segments are perceived as non-collinear by an intervening rectangle, was observed when the rectangle was presented during a period spanning from 50 ms before to 200 ms after the presentation of the line segments. The illusion was most prominent when the rectangle was presented approximately 100 to 150 ms after the line segments. Furthermore, the illusion was observed at the center of a moving object, but only when the line segments were presented before the rectangle. These results indicate that the contents of iconic memory are susceptible to the modulatory influence of subsequent visual inputs before being translated into conscious perception in a time-locked manner both in retinotopic and non-retinotopic, object-centered frames of reference.

Distinct Autistic Traits Are Differentially Associated With the Width of the Multisensory Temporal Binding Window.

Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by deficits in social communication and interaction, and restricted interests and behavior patterns. These characteristics are considered as a continuous distribution in the general population. People with ASD show atypical temporal processing in multisensory integration. Regarding the flash-beep illusion, which refers to how a single flash can be illusorily perceived as multiple flashes when multiple auditory beeps are concurrently presented, some studies reported that people with ASD have a wider temporal binding window and greater integration than typically developed people; others found the opposite or inconsistent tendencies. Here, we investigated the relationships between the manner of the flash-beep illusion and the various dimensions of ASD traits by estimating the degree of typically developed participants' ASD traits including five subscales using the Autism-Spectrum Quotient. We found that stronger ASD traits of communication and social skill were associated with a wider and narrower temporal binding window respectively. These results suggest that specific ASD traits are differently involved in the particular temporal binding processes of audiovisual integration.

An Investigation of the Relationships Between Autistic Traits and Crossmodal Correspondences in Typically Developing Adults.

Autism spectrum disorder (ASD) includes characteristics such as social and behavioral deficits that are considered common across the general population rather than unique to people with the diagnosis. People with ASD are reported to have sensory irregularities, including crossmodal perception. Crossmodal correspondences are phenomena in which arbitrary crossmodal inputs affect behavioral performance. Crossmodal correspondences are considered to be established through associative learning, but the learning cues are considered to differ across the types of correspondences. In order to investigate whether and how ASD traits affect crossmodal associative learning, this study examined the relationships between the magnitude of crossmodal correspondences and the degree of ASD traits among non-diagnosed adults. We found that, among three types of crossmodal correspondences (brightness-loudness, visual size-pitch, and visual location-pitch pairs), the brightness-loudness pair was related with total ASD traits and a subtrait (social skill). The magnitude of newly learned crossmodal associations (the visual apparent motion direction-pitch pair) also showed a relationship with an ASD subtrait (attention switching). These findings demonstrate that there are unique relationships between crossmodal associations and ASD traits, indicating that each ASD trait is differently involved in sensory associative learning.

Neural mechanisms underlying sound-induced visual motion perception: An fMRI study.

Studies of crossmodal interactions in motion perception have reported activation in several brain areas, including those related to motion processing and/or sensory association, in response to multimodal (e.g., visual and auditory) stimuli that were both in motion. Recent studies have demonstrated that sounds can trigger illusory visual apparent motion to static visual stimuli (sound-induced visual motion: SIVM): A visual stimulus blinking at a fixed location is perceived to be moving laterally when an alternating left-right sound is also present. Here, we investigated brain activity related to the perception of SIVM using a 7T functional magnetic resonance imaging technique. Specifically, we focused on the patterns of neural activities in SIVM and visually induced visual apparent motion (VIVM). We observed shared activations in the middle occipital area (V5/hMT), which is thought to be involved in visual motion processing, for SIVM and VIVM. Moreover, as compared to VIVM, SIVM resulted in greater activation in the superior temporal area and dominant functional connectivity between the V5/hMT area and the areas related to auditory and crossmodal motion processing. These findings indicate that similar but partially different neural mechanisms could be involved in auditory-induced and visually-induced motion perception, and neural signals in auditory, visual, and, crossmodal motion processing areas closely and directly interact in the perception of SIVM.

Neural mechanisms underlying touch-induced visual perceptual suppression: An fMRI study.

Crossmodal studies have demonstrated inhibitory as well as facilitatory neural effects in higher sensory association and primary sensory cortices. A recent human behavioral study reported touch-induced visual perceptual suppression (TIVS). Here, we introduced an experimental setting in which TIVS could occur and investigated brain activities underlying visuo-tactile interactions using a functional magnetic resonance imaging technique. While the suppressive effect of touch on vision was only found for half of the participants who could maintain their baseline performance above chance level (i.e. TIVS was not well replicated here), we focused on individual differences in the effect of touch on vision. This effect could be suppressive or enhancement, and the neuronal basis of these differences was analyzed. We found larger inhibitory responses in the anterior part of the right visual cortex (V1, V2) with higher TIVS magnitude when visuo-tactile stimuli were presented as spatially congruent. Activations in the right anterior superior temporal region, including the secondary somatosensory cortical area, were more strongly related to those in the visual cortex (V1, V2) with higher TIVS magnitude. These results indicate that inhibitory neural modulations from somatosensory to visual cortices and the resulting inhibitory neural responses in the visual cortex could be involved in TIVS.