Effect of spatial context on perceived walking direction.

Contextual modulation occurs for many aspects of high-level vision but is relatively unexplored for the perception of walking direction. In a recent study, we observed an effect of the temporal context on perceived walking direction. Here, we examined the spatial contextual modulation by measuring the perceived direction of a target point-light walker in the presence of two flanker walkers, one on each side. Experiment 1 followed a within-subjects design. Participants (n = 30) completed a spatial context task by judging the walking direction of the target in 13 different conditions: a walker alone in the center or with two flanking walkers either intact or scrambled at a flanker deviation of ±15°, ±30°, or ±45°. For comparison, participants completed an adaptation task where they reported the walking direction of a target after adaptation to ±30° walking direction. We found the expected repulsive effects in the adaptation task but attractive effects in the spatial context task. In Experiment 2 (n = 40), we measured the tuning of spatial contextual modulation across a wide range of flanker deviation magnitudes ranging from 15° to 165° in 15° intervals. Our results showed significant attractive effects across a wide range of flanker walking directions with the peak effect at around 30°. The assimilative versus repulsive effects of spatial contextual modulation and temporal adaptation suggest dissociable neural mechanisms, but they may operate on the same population of sensory channels coding for walking direction, as evidenced by similarity in the peak tuning across the walking direction of the inducers.

Detection of Mooney faces is robust to image asymmetries produced by illumination.

Face detection relies on the visual features that are shared across different faces. An important component of the basic spatial configuration of a face is symmetry around the vertical midline. Although human faces are structurally symmetrical, they can be asymmetrical in an image due to the direction of lighting or the position of the face. In the experiments presented here, we examined how face detection from simple contrast patterns that occur across the face is affected by the image asymmetries associated with variations in the horizontal lighting direction. We presented observers with two-tone images of faces (Mooney faces) that isolated the unique pattern of contrast in the shading and shadows on a face, illuminated from a wide range of horizontal directions. In two experiments, we found that face detection is surprisingly robust to these lighting changes, with sensitivity in discriminating between face and non-face patterns reduced only at the most extreme lighting directions. This tolerance to changes in the horizontal lighting direction depended partly on the orientation of the face, vertical lighting direction, and contrast polarity. Our results provide insight into how contrast cues produced by shading and shadows occurring across the facial surface are utilized by the visual system to detect human faces.

Discrimination of facial identity based on simple contrast patterns generated by shading and shadows.

The pattern of shadows and shading across a face is determined partly by face shape and may therefore provide a cue for facial recognition. In this study, we measured the ability of human observers to discriminate facial identity based simply on the coarse pattern of contrast produced by the interaction between facial geometry and lighting direction. We used highly realistic 3D models of human heads to create images of faces illuminated from different horizontal and vertical directions, which were then converted to two-tone images ('Mooney faces') to isolate the coarse pattern of contrast. Participants were presented with pairs of two-tone faces and judged whether it was the same person in both images. Participants could discriminate facial identity based on the minimal cues within the two-tone images, though sensitivity depended on the horizontal and vertical lighting direction. Performance on the Mooney recognition task correlated with general facial recognition ability, though the role of face-specific processing in this relationship was not significant. Our results demonstrate that shading information in the form of simple contrast cues is sufficient for discriminating facial identity, and support the idea that visual processing is somewhat optimised for overhead lighting - here, in the relatively high-level context of face identity recognition.

Adaptation to walking direction in biological motion.

The direction that we see another person walking provides us with an important cue to their intentions, but little is known about how the brain encodes walking direction across a neuronal population. The current study used an adaptation technique to investigate the sensory coding of perceived walking direction. We measured perceived walking direction of point-light stimuli before and after adaptation, and found that adaptation to a specific walking direction resulted in repulsive perceptual aftereffects. The magnitude of these aftereffects was tuned to the walking direction of the adaptor relative to the test, with local repulsion of perceived walking direction for test stimuli oriented on either side of the adapted walking direction. The specific tuning profiles that we observed are well explained by a population-coding model, in which perceived walking direction is coded in terms of the relative activity across a bank of sensory channels with peak tuning distributed across the full 360° range of walking directions. Further experiments showed specificity in how horizontal (azimuth) walking direction is coded when moving away from the observer compared to when moving toward the observer. Moreover, there was clear specificity in these perceptual aftereffects for walking direction compared to a nonbiological form of 3D motion (a rotating sphere). These results indicate the existence of neural mechanisms in the human visual system tuned to specific walking directions, provide insight into the number of sensory channels and how their responses are combined to encode walking direction, and demonstrate the specificity of adaptation to biological motion. (PsycInfo Database Record (c) 2023 APA, all rights reserved).

Gaze behavior as a visual cue to animacy.

A characteristic that distinguishes biological agents from inanimate objects is that the former can have a direction of attention. While it is natural to associate a person's direction of attention with the appearance of their face, attentional behaviors are also a kind of relational motion, in which an entity rotates a specific axis of its form in relation to an independent feature of its environment. Here, we investigated the role of gaze-like motion in providing a visual cue to animacy independent of the human form. We generated animations in which the rotation of a geometric object (the agent) was dependent on the movement of a target. Participants made judgements about how creature-like the objects appeared, which were highly sensitive to the correspondence between objects over and above their individual motion. We varied the dependence between agent rotation and target motion in terms of temporal synchrony, temporal order, cross-correlation, and trajectory complexity. These affected perceptions of animacy to differing extents. When the behavior of the agent was driven by a model of predictive tracking with a sensory sampling delay, perceived animacy was broadly tuned across changes in rotational behavior induced by the sampling delay of the agent. Overall, the tracking relationship provides a salient cue to animacy independent of biological form, provided that temporal synchrony between objects is within a certain range. This motion relationship may be one to which the visual system is highly attuned, due to its association with attentional behavior and the presence of other minds in our environment. (PsycInfo Database Record (c) 2023 APA, all rights reserved).

Spatial selectivity in adaptation to gaze direction.

A person's focus of attention is conveyed by the direction of their eyes and face, providing a simple visual cue fundamental to social interaction. A growing body of research examines the visual mechanisms that encode the direction of another person's gaze as we observe them. Here we investigate the spatial receptive field properties of these mechanisms, by testing the spatial selectivity of sensory adaptation to gaze direction. Human observers were adapted to faces with averted gaze presented in one visual hemifield, then tested in their perception of gaze direction for faces presented in the same or opposite hemifield. Adaptation caused strong, repulsive perceptual aftereffects, but only for faces presented in the same hemifield as the adapter. This occurred even though adapting and test stimuli were in the same external location across saccades. Hence, there was clear evidence for retinotopic adaptation and a relative lack of either spatiotopic or spatially invariant adaptation. These results indicate that adaptable representations of gaze direction in the human visual system have retinotopic spatial receptive fields. This strategy of coding others' direction of gaze with positional specificity relative to one's own eye position may facilitate key functions of gaze perception, such as socially cued shifts in visual attention.

Face detection from patterns of shading and shadows: The role of overhead illumination in generating the familiar appearance of the human face.

Face detection in human vision relies on a stereotypical pattern of visual features common to different faces. How are these visual features generated in the environment? Here we investigate how characteristic patterns of shading and shadows that occur across the face act as a cue for face detection. We use 3D rendering to isolate facial shading under simulated lighting conditions, comparing the broad patterns of contrast that occur across the face when light arrives from different angles. We find that human performance in discriminating faces from non-face objects using these contrast patterns depends strongly on the lighting direction. In particular, light arriving from above the brow tends to facilitate face detection - consistent with the statistics of real-world lighting environments, in which light commonly arrives more strongly from above. Indeed, in a further experiment, we find that asymmetries in lighting that occur in complex and naturalistic lighting environments produce contrast patterns across the face that facilitate face detection. These effects occurred independent of the lighting direction relative to the viewer, suggesting that cues to face detection emerge from the interaction between face morphology and vertical asymmetries in lighting direction, independent of the viewer's knowledge or expectations about lighting direction. Comparison with the performance of an image classifier suggests that the effects of lighting direction partly reflect differences in image information that result from the interaction between shape and illumination, as well as face detection in human observers being better-tuned to the pattern of shading and shadows that occurs across an upright face that is lit from overhead.

Is there a 'zone of eye contact' within the borders of the face?

Eye contact is a salient feature of everyday interactions, yet it is not obvious what the physical conditions are under which we feel that we have eye contact with another person. Here we measure the range of locations that gaze can fall on a person's face to elicit a sense of eye contact. Participants made judgements about eye contact while viewing rendered images of faces with finely-varying gaze direction at a close interpersonal distance (50 cm). The 'zone of eye contact' tends to peak between the two eyes and is often surprisingly narrower than the observer's actual eye region. Indeed, the zone tends to extend further across the face in height than in width. This shares an interesting parallel with the 'cyclopean eye' of visual perspective - our sense of looking out from a single point in space despite the physical separation of our two eyes. The distribution of eye-contact strength across the face can be modelled at the individual-subject level as a 2D Gaussian function. Perception of eye contact is more precise than the sense of having one's face looked at, which captures a wider range of gaze locations in both the horizontal and vertical dimensions, at least at the close viewing distance used in the present study. These features of eye-contact perception are very similar cross-culturally, tested here in Australian and Japanese university students. However, the shape and position of the zone of eye contact does vary depending on recent sensory experience: adaptation to faces with averted gaze causes a pronounced shift and widening of the zone across the face, and judgements about eye contact also show a positive serial dependence. Together, these results provide insight into the conditions under which eye contact is felt, with respect to face morphology, culture, and sensory context.

A sparkle in the eye: Illumination cues and lightness constancy in the perception of eye contact.

In social interactions, our sense of when we have eye contact with another person relies on the distribution of luminance across their eye region, reflecting the position of the darker iris within the lighter sclera of the human eye. This distribution of luminance can be distorted by the lighting conditions, consistent with the fundamental challenge that the visual system faces in distinguishing the nature of a surface from the pattern of light falling upon it. Here we perform a set of psychophysics experiments in human observers to investigate how illumination impacts on the perception of eye contact. First, we find that simple changes in the direction of illumination can produce systematic biases in our sense of when we have eye contact with another person. Second, we find that the visual system uses information about the lighting conditions to partially discount or 'explain away' the effects of illumination in this context, leading to a significantly more robust sense of when we have eye contact with another person. Third, we find that perceived eye contact is affected by specular reflections from the eye surface in addition to shading patterns, implicating eye glint as a potential cue to gaze direction. Overall, this illustrates how our interpretation of social signals relies on visual mechanisms that both compensate for the effects of illumination on retinal input and potentially exploit novel cues that illumination can produce.

Face Pareidolia Recruits Mechanisms for Detecting Human Social Attention.

Face pareidolia is the phenomenon of seeing facelike structures in everyday objects. Here, we tested the hypothesis that face pareidolia, rather than being limited to a cognitive or mnemonic association, reflects the activation of visual mechanisms that typically process human faces. We focused on sensory cues to social attention, which engage cell populations in temporal cortex that are susceptible to habituation effects. Repeated exposure to "pareidolia faces" that appear to have a specific direction of attention causes a systematic bias in the perception of where human faces are looking, indicating that overlapping sensory mechanisms are recruited when we view human faces and when we experience face pareidolia. These cross-adaptation effects are significantly reduced when pareidolia is abolished by removing facelike features from the objects. These results indicate that face pareidolia is essentially a perceptual phenomenon, occurring when sensory input is processed by visual mechanisms that have evolved to extract specific social content from human faces.

A big-data approach to understanding metabolic rate and response to obesity in laboratory mice.

Maintaining a healthy body weight requires an exquisite balance between energy intake and energy expenditure. To understand the genetic and environmental factors that contribute to the regulation of body weight, an important first step is to establish the normal range of metabolic values and primary sources contributing to variability. Energy metabolism is measured by powerful and sensitive indirect calorimetry devices. Analysis of nearly 10,000 wild-type mice from two large-scale experiments revealed that the largest variation in energy expenditure is due to body composition, ambient temperature, and institutional site of experimentation. We also analyze variation in 2329 knockout strains and establish a reference for the magnitude of metabolic changes. Based on these findings, we provide suggestions for how best to design and conduct energy balance experiments in rodents. These recommendations will move us closer to the goal of a centralized physiological repository to foster transparency, rigor and reproducibility in metabolic physiology experimentation.

Maintaining a healthy weight requires the body to balance energy intake and expenditure. The body converts food to energy through a process called energy metabolism. Genetic and environmental factors can affect energy metabolism and energy balance contributing to conditions like obesity. To better understand metabolism, scientists often study mice in laboratories, but mice from different laboratories appear to convert food to energy at different rates. This makes it hard to determine what is 'normal' for mouse metabolism. These discrepancies could be due to small differences between how mice are kept in different laboratories. For example, the temperatures of the mouse cages or how active the mice are might differ depending on the laboratory. Identifying the effects of such differences is essential, but it requires looking at data from hundreds of mice. Corrigan et al. examined data from more than 30,000 mice at laboratories around the world to show that room temperatures and the amount of muscle and fat in a mouse's body have the biggest influence on energy balance. These two factors affected the metabolism of both typical mice and mice with mutations that affect their energy balance. These results suggest that it is important for scientists to report factors like room temperatures, the body make-up of the mice, or the animals' activity levels in metabolism studies. This can help scientists compare results and repeat experiments, which could speed up research into mouse metabolism. Corrigan et al. also found that other unknown factors also affect mouse metabolism in different laboratories. Further studies are needed to identify these factors.

Adaptation to the Direction of Others' Gaze: A Review.

The direction of another person's gaze provides us with a strong cue to their intentions and future actions, and, correspondingly, the human visual system has evolved to extract information about others' gaze from the sensory stream. The perception of gaze is a remarkably plastic process: adaptation to a particular direction of gaze over a matter of seconds or minutes can cause marked aftereffects in our sense of where other people are looking. In this review, we first discuss the measurement, specificity, and neural correlates of gaze aftereffects. We then examine how studies that have explored the perceptual and neural determinants of gaze aftereffects have provided key insights into the nature of how other people's gaze direction is represented within the visual hierarchy. This includes the level of perceptual representation of gaze direction (e.g., relating to integrated vs. local facial features) and the interaction of this system with higher-level social-cognitive functions, such as theory of mind. Moreover, computational modeling of data from behavioral studies of gaze adaptation allows us to make inferences about the functional principles that govern the neural encoding of gaze direction. This in turn provides a foundation for testing computational theories of neuropsychiatric conditions in which gaze processing is compromised, such as autism.

Deep Brain Stimulation for Parkinson's disease changes perception in the Rubber Hand Illusion.

Parkinson's disease (PD) alters cortico-basal ganglia-thalamic circuitry and susceptibility to an illusion of bodily awareness, the Rubber Hand Illusion (RHI). Bodily awareness is thought to result from multisensory integration in a predominantly cortical network; the role of subcortical connections is unknown. We studied the effect of modulating cortico-subcortical circuitry on multisensory integration for bodily awareness in 24 PD patients treated with subthalamic nucleus (STN) deep brain stimulation (DBS), in comparison to 21 healthy volunteers, using the RHI experiment. Typically, synchronous visuo-tactile cues induce a false perception of touch on the rubber hand as if it were the subject's hand, whereas asynchronous visuo-tactile cues do not. However, we found that in the asynchronous condition, patients in the off-stimulation state did not reject the RHI as strongly as healthy controls; patients' rejection of the RHI strengthened when STN-DBS was switched on, although it remained weaker than that of controls. Patients in the off-stimulation state also misjudged the position of their hand, indicating it to be closer to the rubber hand than controls. However, STN-DBS did not affect proprioceptive judgements or subsequent arm movements altered by the perceptual effects of the illusion. Our findings support the idea that the STN and subcortical connections have a key role in multisensory integration for bodily awareness. Decision-making in multisensory bodily illusions is discussed.

Adaptation to other people's eye gaze reflects habituation of high-level perceptual representations.

Our sense of where another person is looking depends upon multiple features of their face, relating to both the deviation of their eyes and the angle of their head. In this way, gaze direction is a higher-level perceptual property that is dependent on holistic processing of lower-level visual cues. A key paradigm in social perception research is sensory adaptation, which has been used to probe how properties like gaze direction are encoded in the visual system. Here we test whether sensory adaptation acts on higher-level, perceptual representations of gaze direction, or occurs to lower-level visual features of the face alone. To this end, participants were adapted on faces that evoke the Wollaston illusion, in which the direction that the face appears to look differs from its veridical eye direction. We compared across sets of images that were exactly matched in the lower-level features of the face image, but perceptually distinct due to differences in the conjunction of head and eye direction. The changes in participants' perception of gaze direction following adaptation were consistent with habituation having occurred to the perceived gaze direction of the Wollaston faces, where this is dependent on integration of eye direction and head direction, rather than to lower-level sensory features of the face alone. This constitutes strong evidence for adaptable representations of other people's gaze direction in the visual system that are abstracted from lower-level facial cues.

Phosphorylation of Beta-3 adrenergic receptor at serine 247 by ERK MAP kinase drives lipolysis in obese adipocytes.

OBJECTIVE: The inappropriate release of free fatty acids from obese adipose tissue stores has detrimental effects on metabolism, but key molecular mechanisms controlling FFA release from adipocytes remain undefined. Although obesity promotes systemic inflammation, we find activation of the inflammation-associated Mitogen Activated Protein kinase ERK occurs specifically in adipose tissues of obese mice, and provide evidence that adipocyte ERK activation may explain exaggerated adipose tissue lipolysis observed in obesity. METHODS AND RESULTS: We provide genetic and pharmacological evidence that inhibition of the MEK/ERK pathway in human adipose tissue, mice, and flies all effectively limit adipocyte lipolysis. In complementary findings, we show that genetic and obesity-mediated activation of ERK enhances lipolysis, whereas adipose tissue specific knock-out of ERK2, the exclusive ERK1/2 protein in adipocytes, dramatically impairs lipolysis in explanted mouse adipose tissue. In addition, acute inhibition of MEK/ERK signaling also decreases lipolysis in adipose tissue and improves insulin sensitivity in obese mice. Mice with decreased rates of adipose tissue lipolysis in vivo caused by either MEK or ATGL pharmacological inhibition were unable to liberate sufficient White Adipose Tissue (WAT) energy stores to fuel thermogenesis from brown fat during a cold temperature challenge. To identify a molecular mechanism controlling these actions, we performed unbiased phosphoproteomic analysis of obese adipose tissue at different time points following acute pharmacological MEK/ERK inhibition. MEK/ERK inhibition decreased levels of adrenergic signaling and caused de-phosphorylation of the ß3-adrenergic receptor (ß3AR) on serine 247. To define the functional implications of this phosphorylation, we showed that CRISPR/Cas9 engineered cells expressing wild type ß3AR exhibited ß3AR phosphorylation by ERK2 and enhanced lipolysis, but this was not seen when serine 247 of ß3AR was mutated to alanine. CONCLUSION: Taken together, these data suggest that ERK activation in adipocytes and subsequent phosphorylation of the ß3AR on S247 are critical regulatory steps in the enhanced adipocyte lipolysis of obesity.

Biases in perceiving gaze vergence.

The focus of another person's gaze is an important cue in social interactions, helping us to understand others' intentions, predict their behavior, and allocate our own attention appropriately. The perception of gaze vergence provides information about the distance at which another person is fixating, but has yet to receive much empirical attention. Here, we report that observers display systematic biases when perceiving others' gaze vergence and depth of fixation. Specifically, they perceive others as having convergent gaze and fixating at closer distances, especially when gaze is directed downward or observed under conditions of sensory uncertainty. These biases may reflect the predominance of convergent over divergent gaze in everyday social interactions and implicit knowledge of the physical structure of the environment, in which objects below our line of sight are typically closer. These findings demonstrate the sophistication of social vision, in which our visual perception of others is shaped by statistical regularities, and help to establish the perception of others' gaze vergence and fixation distance as a subject of psychological investigation. (PsycINFO Database Record

Autistic adults show preserved normalisation of sensory responses in gaze processing.

Progress in our understanding of autism spectrum disorder (ASD) has recently been sought by characterising how systematic differences in canonical neural computations employed across the sensory cortex might contribute to clinical symptoms in diverse sensory, cognitive, and social domains. A key proposal is that ASD is characterised by reduced divisive normalisation of sensory responses. This provides a bridge between genetic and molecular evidence for an increased ratio of cortical excitation to inhibition in ASD and the functional characteristics of sensory coding that are relevant for understanding perception and behaviour. Here we tested this hypothesis in the context of gaze processing (i.e., the perception of other people's direction of gaze), a domain with direct relevance to the core diagnostic features of ASD. We show that reduced divisive normalisation in gaze processing is associated with specific predictions regarding the psychophysical effects of sensory adaptation to gaze direction, and test these predictions in adults with ASD. We report compelling evidence that both divisive normalisation and sensory adaptation occur robustly in adults with ASD in the context of gaze processing. These results have important theoretical implications for defining the types of divisive computations that are likely to be intact or compromised in this condition (e.g., relating to local vs distal control of cortical gain). These results are also a strong testament to the typical sensory coding of gaze direction in ASD, despite the atypical responses to others' gaze that are a hallmark feature of this diagnosis.

Perceptual integration of head and eye cues to gaze direction in schizophrenia.

The perceptual mechanisms that underlie social experience in schizophrenia are increasingly becoming a target of empirical research. In the context of low-level vision, there is evidence for a reduction in the integration of sensory features in schizophrenia (e.g. increased thresholds for contour detection and motion coherence). In the context of higher-level vision, comparable differences in the integration of sensory features of the face could in theory impair the recognition of important social cues. Here we examine how the sense of where other people are looking relies upon the integration of eye-region cues and head-region cues. Adults with schizophrenia viewed face images designed to elicit the 'Wollaston illusion', a perceptual phenomenon in which the perceived gaze direction associated with a given pair of eyes is modulated by the surrounding sensory context. We performed computational modelling of these psychophysical data to quantify individual differences in the use of facial cues to gaze direction. We find that adults with schizophrenia exhibit a robust perceptual effect whereby their sense of other people's direction of gaze is strongly biased by sensory cues relating to head orientation in addition to eye region information. These results indicate that the visual integration of facial cues to gaze direction in schizophrenia is intact, helping to constrain theories of reduced integrative processing in higher-level and lower-level vision. In addition, robust gaze processing was evident in the tested participants despite reduced performance on a theory of mind task designed to assess higher-level social cognition.

Adaptive sensory coding of gaze direction in schizophrenia.

Schizophrenia has been associated with differences in how the visual system processes sensory input. A fundamental mechanism that regulates sensory processing in the brain is gain control, whereby the responses of sensory neurons to a given stimulus are modulated in accordance with the spatial and temporal context. Some studies indicate an impairment of certain cortical gain control mechanisms in schizophrenia in low-level vision, reflected, for instance, in how the visual appearance of a stimulus is affected by the presence of other stimuli around it. In the present study, we investigated higher-level, social vision in schizophrenia, namely the perception of other people's direction of gaze (i.e. a type of face processing). Recent computational modelling work indicates that perceptual aftereffects-changes in perception that occur following repeated exposure to faces that display a specific direction of gaze-are indicative of two distinct forms of gain control involved in the coding of gaze direction across sensory neurons. We find that individuals with schizophrenia display strong perceptual aftereffects following repeated exposure to faces with averted gaze, and a modelling analysis indicates similarly robust gain control in the form of (i) short-term adjustment of channel sensitivities in response to the recent sensory history and (ii) divisive normalization of the encoded gaze direction. Together, this speaks to the typical coding of other people's direction of gaze in the visual system in schizophrenia, including flexible gain control, despite the social-cognitive impairments that can occur in this condition.