Testing visual self-misperception in anorexia nervosa using a symmetrical body size estimation paradigm.

OBJECTIVE: Individuals diagnosed with anorexia nervosa (AN) often report seeing themselves as overweight. While body size estimation tasks suggest that such individuals overestimate their body size, these tasks have failed to establish whether this misestimation stems from visual misperception. Misestimation might, instead, be due to response bias. We designed a paradigm to distinguish between visual and response bias contributions to body size misestimation: the symmetrical body size estimation (s-BSE) paradigm. METHOD: The s-BSE paradigm involves two tasks. In the conventional task, participants estimate the width of their photographed body by adjusting the size of a rectangle to match. In the transposed task, participants adjust the size of a photograph of their body to match the rectangle. If overestimation stems exclusively from visual misperception, then errors in each task would be equal and opposite. Using this paradigm, we compared the performance of women diagnosed with AN (n = 14) against women without any eating disorder (n = 40). RESULTS: In the conventional task, we replicated previous findings indicating that both women with AN and women without any eating disorder overestimate their body size. In the transposed task, neither group adjusted the bodies to be narrower than the rectangle. Participants with AN set their photographs to be significantly wider. DISCUSSION: While we replicated previous findings of body size overestimation amongst women with AN and those without any eating disorder, our results are inconsistent with the hypothesis that such overestimation stems exclusively from visual misperception and instead suggest a substantial response bias effect. PUBLIC SIGNIFICANCE: Women with anorexia nervosa overestimate their own body size. Research has not yet determined whether this overestimation stems from them seeing themselves as larger or other, non-visual factors. We employ a new method for distinguishing these possibilities and find that non-visual factors influence size estimates for women with and without anorexia nervosa. This method can help future research control for non-perceptual influences on participant responses.

Vicarious touch: Overlapping neural patterns between seeing and feeling touch.

Simulation theories propose that vicarious touch arises when seeing someone else being touched triggers corresponding representations of being touched. Prior electroencephalography (EEG) findings show that seeing touch modulates both early and late somatosensory responses (measured with or without direct tactile stimulation). Functional Magnetic Resonance Imaging (fMRI) studies have shown that seeing touch increases somatosensory cortical activation. These findings have been taken to suggest that when we see someone being touched, we simulate that touch in our sensory systems. The somatosensory overlap when seeing and feeling touch differs between individuals, potentially underpinning variation in vicarious touch experiences. Increases in amplitude (EEG) or cerebral blood flow response (fMRI), however, are limited in that they cannot test for the information contained in the neural signal: seeing touch may not activate the same information as feeling touch. Here, we use time-resolved multivariate pattern analysis on whole-brain EEG data from people with and without vicarious touch experiences to test whether seen touch evokes overlapping neural representations with the first-hand experience of touch. Participants felt touch to the fingers (tactile trials) or watched carefully matched videos of touch to another person's fingers (visual trials). In both groups, EEG was sufficiently sensitive to allow decoding of touch location (little finger vs. thumb) on tactile trials. However, only in individuals who reported feeling touch when watching videos of touch could a classifier trained on tactile trials distinguish touch location on visual trials. This demonstrates that, for people who experience vicarious touch, there is overlap in the information about touch location held in the neural patterns when seeing and feeling touch. The timecourse of this overlap implies that seeing touch evokes similar representations to later stages of tactile processing. Therefore, while simulation may underlie vicarious tactile sensations, our findings suggest this involves an abstracted representation of directly felt touch.

Interoceptive Abnormalities and Suicidality: A Systematic Review.

Dysfunction of interoception (i.e., difficulties sensing the physiological state of one's own body) is increasingly linked to different mental health disorders and suicidal outcomes. The aim of this study was to systematically review the literature on the association between suicidality and interoception, as well as identify potential confounders and mediators of the relationship. We conducted a systematic review of four databases, allowing for critical examination of the role of different measures of interoception (accuracy, sensibility, awareness, cognitive/emotional evaluation) across the suicide continuum (ideation, plans, attempts, deaths). The search strategy identified 22 studies (14,988 participants). Preliminary but limited evidence was found for impaired interoceptive accuracy among those reporting suicide attempt histories. We found evidence of interoceptive sensibility disturbances across the suicide continuum, including experiences of not trusting one's own body sensations and impaired abilities to sustain and control attention to such sensations. Consistent evidence was also reported for disturbances related to cognitive and emotional evaluations of interoceptive sensations. The latter was particularly pronounced for those reporting suicide attempts, relative to those reporting suicidal thinking or planning alone. Overall, this review's results suggest that interoceptive abnormalities are potentially important indicators of risk for suicidal thinking, intentions, and behaviors. However, due to the inconsistent adjustment for variables of interest, and cross-sectional designs, it is unclear whether interoceptive changes and disturbances have a direct role, or whether the association is explained and mediated by key third variables (e.g. depression, disordered eating, emotional dysregulation). We discuss the implications with respect to suicidal risk and therapeutic interventions.

Visual body-size adaptation and estimation of tactile distance.

Estimating the size of bodies is crucial for interactions with physical and social environments. Body-size perception is malleable and can be altered using visual adaptation paradigms. However, it is unclear whether such visual adaptation effects also transfer to other modalities and influence, for example, the perception of tactile distances. In this study, we employed a visual adaptation paradigm. Participants were exposed to images of expanded or contracted versions of self- or other-identity bodies. Before and after this adaptation, they were asked to manipulate the width of body stimuli to appear as 'normal' as possible. We replicated an effect of visual adaptation such that the body-size selected as most 'normal' was larger after exposure to expanded and thinner after exposure to contracted adaptation stimuli. In contrast, we did not find evidence that this adaptation effect transfers to distance estimates for paired tactile stimuli delivered to the abdomen. A Bayesian analysis showed that our data provide moderate evidence that there is no effect of visual body-size adaptation on the estimation of spatial parameters in a tactile task. This suggests that visual body-size adaptation effects do not transfer to somatosensory body-size representations.

Cortical thinning and associated connectivity changes in patients with anorexia nervosa.

Structural brain abnormalities are a consistent finding in anorexia nervosa (AN) and proposed as a state biomarker of the disorder. Yet little is known about how regional structural changes affect intrinsic resting-state functional brain connectivity (rsFC). Using a cross-sectional, multimodal imaging approach, we investigated the association between regional cortical thickness abnormalities and rsFC in AN. Twenty-two acute AN patients and twenty-six age- and gender-matched healthy controls underwent a resting-state functional magnetic resonance imaging scan and cognitive tests. We performed group comparisons of whole-brain cortical thickness, seed-based rsFC, and network-based statistical (NBS) analyses. AN patients showed cortical thinning in the precuneus and inferior parietal lobules, regions involved in visuospatial memory and imagery. Cortical thickness in the precuneus correlated with nutritional state and cognitive functions in AN, strengthening the evidence for a critical role of this region in the disorder. Cortical thinning was accompanied by functional connectivity reductions in major brain networks, namely default mode, sensorimotor and visual networks. Similar to the seed-based approach, the NBS analysis revealed a single network of reduced functional connectivity in patients, comprising mainly sensorimotor- occipital regions. Our findings provide evidence that structural and functional brain abnormalities in AN are confined to specific regions and networks involved in visuospatial and somatosensory processing. We show that structural changes of the precuneus are linked to nutritional and functional states in AN, and future longitudinal research should assess how precuneus changes might be related to the evolution of the disorder.

Perception of visual-tactile asynchrony, bodily perceptual aberrations, and bodily illusions in schizophrenia.

Body perception can be altered in individuals with schizophrenia resulting in experiences of undefined boundaries, loss of ownership, and size changes. These individuals may also be more susceptible to the rubber hand illusion (RHI: an illusion of body perception that can also be induced in neurotypical populations), but the findings are mixed. Furthermore, the perception of multisensory timing, which is thought to be fundamental for body perception, is altered in schizophrenia. We tested whether altered perception of the temporal relationship between visual and tactile signals in schizophrenia predicts self-reported perceptual aberrations and RHI susceptibility. We found that the sensitivity to detect temporal asynchronies is reduced in schizophrenia and this is a significant predictor for bodily perceptual symptoms. In contrast, we found no evidence for a direct relationship between asynchrony detection sensitivity and RHI susceptibility. Instead, our findings suggest that experiencing more bodily perceptual symptoms increases the likelihood of endorsing unusual bodily experiences, resulting in higher RHI self-ratings but not higher proprioceptive drift scores. Our findings provide new insight into factors that may underlie the report of unusual body perceptions in schizophrenia.

Visual body form and orientation cues do not modulate visuo-tactile temporal integration.

Body ownership relies on spatiotemporal correlations between multisensory signals and visual cues specifying oneself such as body form and orientation. The mechanism for the integration of bodily signals remains unclear. One approach to model multisensory integration that has been influential in the multisensory literature is Bayesian causal inference. This specifies that the brain integrates spatial and temporal signals coming from different modalities when it infers a common cause for inputs. As an example, the rubber hand illusion shows that visual form and orientation cues can promote the inference of a common cause (one's body) leading to spatial integration shown by a proprioceptive drift of the perceived location of the real hand towards the rubber hand. Recent studies investigating the effect of visual cues on temporal integration, however, have led to conflicting findings. These could be due to task differences, variation in ecological validity of stimuli and/or small samples. In this pre-registered study, we investigated the influence of visual information on temporal integration using a visuo-tactile temporal order judgement task with realistic stimuli and a sufficiently large sample determined by Bayesian analysis. Participants viewed videos of a touch being applied to plausible or implausible visual stimuli for one's hand (hand oriented plausibly, hand rotated 180 degrees, or a sponge) while also being touched at varying stimulus onset asynchronies. Participants judged which stimulus came first: viewed or felt touch. Results show that visual cues do not modulate visuo-tactile temporal order judgements. This is not in line with the idea that bodily signals indicating oneself influence the integration of multisensory signals in the temporal domain. The current study emphasises the importance of rigour in our methodologies and analyses to advance the understanding of how properties of multisensory events affect the encoding of temporal information in the brain.

Limits on visual awareness of object targets in the context of other object category masks: Investigating bottlenecks in the continuous flash suppression paradigm with hand and tool stimuli.

The continuous flash suppression (CFS) task can be used to investigate what limits our capacity to become aware of visual stimuli. In this task, a stream of rapidly changing mask images to one eye initially suppresses awareness for a static target image presented to the other eye. Several factors may determine the breakthrough time from mask suppression, one of which is the overlap in representation of the target/mask categories in higher visual cortex. This hypothesis is based on certain object categories (e.g., faces) being more effective in blocking awareness of other categories (e.g., buildings) than other combinations (e.g., cars/chairs). Previous work found mask effectiveness to be correlated with category-pair high-level representational similarity. As the cortical representations of hands and tools overlap, these categories are ideal to test this further as well as to examine alternative explanations. For our CFS experiments, we predicted longer breakthrough times for hands/tools compared to other pairs due to the reported cortical overlap. In contrast, across three experiments, participants were generally faster at detecting targets masked by hands or tools compared to other mask categories. Exploring low-level explanations, we found that the category average for edges (e.g., hands have less detail compared to cars) was the best predictor for the data. This low-level bottleneck could not completely account for the specific category patterns and the hand/tool effects, suggesting there are several levels at which object category-specific limits occur. Given these findings, it is important that low-level bottlenecks for visual awareness are considered when testing higher-level hypotheses.

When the body is the target-Representations of one's own body and bodily sensations in self-harm: A systematic review.

BACKGROUND: Typically, we try to protect our own bodies and this is supported by internal representations that specify one's body identity, spatial parameters, and bodily sensations, but in self-harm the body becomes the target. First acts of self-harm are typically reported in adolescence. At this age, the body also becomes more salient to one's self-concept. It may be possible that disturbances in representations of one's own body and its sensations contribute to self-harm. METHODS: To investigate these links, we conducted a systematic review critically examining the potential role of body representation and sensation disturbances in self-harm (non-suicidal or suicidal) in adolescents and young adults (12-25 years). RESULTS: The search strategy identified 64 studies (275,183 participants) and overall, young people engaging in self-harm reported greater levels of body dissatisfaction, body disownership, and deficits in the experience and evaluation of bodily sensations compared to non-injuring control groups; however, there was subscale variability and gender differences. CONCLUSION: Our results emphasise the strong link between body representations and self-protection, as well as a need for investigating self-harm interventions that take body image and awareness into account.

Representing the location of manipulable objects in shape-selective occipitotemporal cortex: Beyond retinotopic reference frames?

When interacting with objects, we have to represent their location relative to our bodies. To facilitate bodily reactions, location may be encoded in the brain not just with respect to the retina (retinotopic reference frame), but also in relation to the head, trunk or arm (collectively spatiotopic reference frames). While spatiotopic reference frames for location encoding can be found in brain areas for action planning, such as parietal areas, there is debate about the existence of spatiotopic reference frames in higher-level occipitotemporal visual areas. In an extensive multi-voxel pattern analysis (MVPA) fMRI study using faces, headless bodies and scenes stimuli, Golomb and Kanwisher (2012) did not find evidence for spatiotopic reference frames in shape-selective occipitotemporal cortex. This finding is important for theories of how stimulus location is encoded in the brain. It is possible, however, that their failure to find spatiotopic reference frames is related to their stimuli: we typically do not manipulate faces, headless bodies or scenes. It is plausible that we only represent body-centred location when viewing objects that are typically manipulated. Here, we tested for object location encoding in shape-selective occipitotemporal cortex using manipulable object stimuli (balls and cups) in a MVPA fMRI study. We employed Bayesian analyses to determine sample size and evaluate the sensitivity of our data to test the hypothesis that location can be encoded in a spatiotopic reference frame in shape-selective occipitotemporal cortex over the null hypothesis of no spatiotopic location encoding. We found strong evidence for retinotopic location encoding consistent with previous findings that retinotopic reference frames are common neural representations of object location. In contrast, when testing for spatiotopic encoding, we found evidence that object location information for small manipulable objects is not decodable in relation to the body in shape-selective occipitotemporal cortex. Post-hoc exploratory analyses suggested that spatiotopic aspects might modulate retinotopic location encoding. Overall, our findings provide evidence that there is no spatiotopic encoding that is independent of retinotopic location in shape-selective occipitotemporal cortex.

Multisensory temporal processing in own-body contexts: plausibility of hand ownership does not improve visuo-tactile asynchrony detection.

Tracking one's own body is essential for environmental interaction, and involves integrating multisensory cues with stored information about the body's typical features. Exactly how multisensory information is integrated in own-body perception is still unclear. For example, Ide and Hidaka (Exp Brain Res 228:43-50, 2013) found that participants made less precise visuo-tactile temporal order judgments (TOJ) when viewing hands in a plausible orientation (upright; typical for one's own hand) compared to an implausible orientation (rotated 180°). This suggests that viewing one's own body relaxes the precision for perceived visuo-tactile synchrony. In contrast, visuo-proprioceptive research shows improvements for multisensory temporal perception near one's own body in asynchrony detection tasks, implying an increase in precision. Hence, it is unclear whether viewed hand orientation generally modulates the ability to detect small asynchronies between vision and touch, or if this effect is specific to TOJ tasks. We investigated whether viewed hand orientation affects detection of visuo-tactile asynchrony. In two experiments, participants viewed model hands in anatomically plausible or implausible orientations. In one experiment, we stroked the hands to induce the rubber hand illusion. Participants were asked to detect short delays (40-280 ms) between vision (an LED flash on the model hand) and touch (a tap to fingertip of the participant's hidden hand) in a two-interval forced-choice task. Bayesian analyses show that our data provide strong evidence that viewed hand orientation does not affect visuo-tactile asynchrony detection. This study suggests the mechanisms for fine-grained time perception differ between visuo-tactile and visuo-proprioceptive contexts.

Revisiting the link between body and agency: visual movement congruency enhances intentional binding but is not body-specific.

Embodiment and agency are key aspects of how we perceive ourselves that have typically been associated with independent mechanisms. Recent work, however, has suggested that these mechanisms are related. The sense of agency arises from recognising a causal influence on the external world. This influence is typically realised through bodily movements and thus the perception of the bodily self could also be crucial for agency. We investigated whether a key index of agency - intentional binding - was modulated by body-specific information. Participants judged the interval between pressing a button and a subsequent tone. We used virtual reality to manipulate two aspects of movement feedback. First, form: participants viewed a virtual hand or sphere. Second, movement congruency: the viewed object moved congruently or incongruently with the participant's hidden hand. Both factors, form and movement congruency, significantly influenced embodiment. However, only movement congruency influenced intentional binding. Binding was increased for congruent compared to incongruent movement feedback irrespective of form. This shows that the comparison between viewed and performed movements provides an important cue for agency, whereas body-specific visual form does not. We suggest that embodiment and agency mechanisms both depend on comparisons across sensorimotor signals but that they are influenced by distinct factors.

Multisensory coding in the multiple-demand regions: vibrotactile task information is coded in frontoparietal cortex.

At any given moment, our brains receive input from multiple senses. Successful behavior depends on our ability to prioritize the most important information and ignore the rest. A multiple-demand (MD) network of frontal and parietal regions is thought to support this process by adjusting to code information that is currently relevant (Duncan 2010). Accordingly, the network is proposed to encode a range of different types of information, including perceptual stimuli, task rules, and responses, as needed for the current cognitive operation. However, most MD research has used visual tasks, leaving limited information about whether these regions encode other sensory domains. We used multivoxel pattern analysis (MVPA) of functional magnetic resonance imaging (fMRI) data to test whether the MD regions code the details of somatosensory stimuli, in addition to tactile-motor response transformation rules and button-press responses. Participants performed a stimulus-response task in which they discriminated between two possible vibrotactile frequencies and applied a stimulus-response transformation rule to generate a button-press response. For MD regions, we found significant coding of tactile stimulus, rule, and response. Primary and secondary somatosensory regions encoded the tactile stimuli and the button-press responses but did not represent task rules. Our findings provide evidence that MD regions can code nonvisual somatosensory task information, commensurate with a domain-general role in cognitive control.NEW & NOTEWORTHY How does the brain encode the breadth of information from our senses and use this to produce goal-directed behavior? A network of frontoparietal multiple-demand (MD) regions is implicated but has been studied almost exclusively in the context of visual tasks. We used multivariate pattern analysis of fMRI data to show that these regions encode tactile stimulus information, rules, and responses. This provides evidence for a domain-general role of the MD network in cognitive control.

Non-hierarchical Influence of Visual Form, Touch, and Position Cues on Embodiment, Agency, and Presence in Virtual Reality.

The concept of self-representation is commonly decomposed into three component constructs (sense of embodiment, sense of agency, and sense of presence), and each is typically investigated separately across different experimental contexts. For example, embodiment has been explored in bodily illusions; agency has been investigated in hypnosis research; and presence has been primarily studied in the context of Virtual Reality (VR) technology. Given that each component involves the integration of multiple cues within and across sensory modalities, they may rely on similar underlying mechanisms. However, the degree to which this may be true remains unclear when they are independently studied. As a first step toward addressing this issue, we manipulated a range of cues relevant to these components of self-representation within a single experimental context. Using consumer-grade Oculus Rift VR technology, and a new implementation of the Virtual Hand Illusion, we systematically manipulated visual form plausibility, visual-tactile synchrony, and visual-proprioceptive spatial offset to explore their influence on self-representation. Our results show that these cues differentially influence embodiment, agency, and presence. We provide evidence that each type of cue can independently and non-hierarchically influence self-representation yet none of these cues strictly constrains or gates the influence of the others. We discuss theoretical implications for understanding self-representation as well as practical implications for VR experiment design, including the suitability of consumer-based VR technology in research settings.

Body distortions in Anorexia Nervosa: Evidence for changed processing of multisensory bodily signals.

Body size and shape distortion is a core feature of Anorexia Nervosa (AN) - patients experience their body as fat while objectively being very thin. The cause of this distortion is unclear and disturbances in body perception could be involved. Body perception comprises estimating shape and location of one's body and requires integrating multisensory signals. We investigated if and how body location perception is changed and tested 23 AN patients and 23 healthy controls (HC) in a Rubber Hand Illusion (RHI) reaching paradigm. We presented two types of multisensory conflicts (visual-proprioceptive hand location; visual-tactile touch synchrony) and tested if the impact of visual-proprioceptive and visual-tactile signals on hand location perception differs between AN and HC groups. We found significant group differences in shifts of reaching trajectories, indicating that the influence of proprioceptive signals on hand location estimates is reduced in AN. Hand location estimates were relatively more biased towards external visual information, and shorter illness durations predicted a larger visual bias. Although touch synchrony also significantly influenced hand location estimates, this effect did not differ between groups. Our findings provide compelling evidence that multisensory body location perception - specifically the processing of visual-proprioceptive signals - is changed in AN.

The plausibility of visual information for hand ownership modulates multisensory synchrony perception.

We are frequently changing the position of our bodies and body parts within complex environments. How does the brain keep track of one's own body? Current models of body ownership state that visual body ownership cues such as viewed object form and orientation are combined with multisensory information to correctly identify one's own body, estimate its current location and evoke an experience of body ownership. Within this framework, it may be possible that the brain relies on a separate perceptual analysis of body ownership cues (e.g. form, orientation, multisensory synchrony). Alternatively, these cues may interact in earlier stages of perceptual processing-visually derived body form and orientation cues may, for example, directly modulate temporal synchrony perception. The aim of the present study was to distinguish between these two alternatives. We employed a virtual hand set-up and psychophysical methods. In a two-interval force-choice task, participants were asked to detect temporal delays between executed index finger movements and observed movements. We found that body-specifying cues interact in perceptual processing. Specifically, we show that plausible visual information (both form and orientation) for one's own body led to significantly better detection performance for small multisensory asynchronies compared to implausible visual information. We suggest that this perceptual modulation when visual information plausible for one's own body is present is a consequence of body-specific sensory predictions.

Manipulating motor performance and memory through real-time fMRI neurofeedback.

Task performance depends on ongoing brain activity which can be influenced by attention, arousal, or motivation. However, such modulating factors of cognitive efficiency are unspecific, can be difficult to control, and are not suitable to facilitate neural processing in a regionally specific manner. Here, we non-pharmacologically manipulated regionally specific brain activity using technically sophisticated real-time fMRI neurofeedback. This was accomplished by training participants to simultaneously control ongoing brain activity in circumscribed motor and memory-related brain areas, namely the supplementary motor area and the parahippocampal cortex. We found that learned voluntary control over these functionally distinct brain areas caused functionally specific behavioral effects, i.e. shortening of motor reaction times and specific interference with memory encoding. The neurofeedback approach goes beyond improving cognitive efficiency by unspecific psychological factors such as attention, arousal, or motivation. It allows for directly manipulating sustained activity of task-relevant brain regions in order to yield specific behavioral or cognitive effects.

The crossmodal congruency task as a means to obtain an objective behavioral measure in the rubber hand illusion paradigm.

The rubber hand illusion (RHI) is a popular experimental paradigm. Participants view touch on an artificial rubber hand while the participants' own hidden hand is touched. If the viewed and felt touches are given at the same time then this is sufficient to induce the compelling experience that the rubber hand is one's own hand. The RHI can be used to investigate exactly how the brain constructs distinct body representations for one's own body. Such representations are crucial for successful interactions with the external world. To obtain a subjective measure of the RHI, researchers typically ask participants to rate statements such as "I felt as if the rubber hand were my hand". Here we demonstrate how the crossmodal congruency task can be used to obtain an objective behavioral measure within this paradigm. The variant of the crossmodal congruency task we employ involves the presentation of tactile targets and visual distractors. Targets and distractors are spatially congruent (i.e. same finger) on some trials and incongruent (i.e. different finger) on others. The difference in performance between incongruent and congruent trials - the crossmodal congruency effect (CCE) - indexes multisensory interactions. Importantly, the CCE is modulated both by viewing a hand as well as the synchrony of viewed and felt touch which are both crucial factors for the RHI. The use of the crossmodal congruency task within the RHI paradigm has several advantages. It is a simple behavioral measure which can be repeated many times and which can be obtained during the illusion while participants view the artificial hand. Furthermore, this measure is not susceptible to observer and experimenter biases. The combination of the RHI paradigm with the crossmodal congruency task allows in particular for the investigation of multisensory processes which are critical for modulations of body representations as in the RHI.

Preference for orientations commonly viewed for one's own hand in the anterior intraparietal cortex.

Brain regions in the intraparietal and the premotor cortices selectively process visual and multisensory events near the hands (peri-hand space). Visual information from the hand itself modulates this processing potentially because it is used to estimate the location of one's own body and the surrounding space. In humans specific occipitotemporal areas process visual information of specific body parts such as hands. Here we used an fMRI block-design to investigate if anterior intraparietal and ventral premotor 'peri-hand areas' exhibit selective responses to viewing images of hands and viewing specific hand orientations. Furthermore, we investigated if the occipitotemporal 'hand area' is sensitive to viewed hand orientation. Our findings demonstrate increased BOLD responses in the left anterior intraparietal area when participants viewed hands and feet as compared to faces and objects. Anterior intraparietal and also occipitotemporal areas in the left hemisphere exhibited response preferences for viewing right hands with orientations commonly viewed for one's own hand as compared to uncommon own hand orientations. Our results indicate that both anterior intraparietal and occipitotemporal areas encode visual limb-specific shape and orientation information.

From head to toe: evidence for selective brain activation reflecting visual perception of whole individuals.

Our ability to recognize other people's faces and bodies is crucial for our social interactions. Previous neuroimaging studies have repeatedly demonstrated the existence of brain areas that selectively respond to visually presented faces and bodies. In daily life, however, we see "whole" people and not just isolated faces and bodies, and the question remains of how information from these two categories of stimuli is integrated at a neural level. Are faces and bodies merely processed independently, or are there neural populations that actually code for whole individuals? In the current study we addressed this question using a functional magnetic resonance imaging adaptation paradigm involving the sequential presentation of visual stimuli depicting whole individuals. It is known that adaptation effects for a component of a stimulus only occur in neural populations that are sensitive to that particular component. The design of our experiment allowed us to measure adaptation effects occurring when either just the face, just the body, or both the face and the body of an individual were repeated. Crucially, we found novel evidence for the existence of neural populations in fusiform as well as extrastriate regions that showed selective adaptation for whole individuals, which could not be merely explained by the sum of adaptation for face and body respectively. The functional specificity of these neural populations is likely to support fast and accurate recognition and integration of information conveyed by both faces and bodies. Hence, they can be assumed to play an important role for identity as well as emotion recognition in everyday life.