Putting people in context: ERP responses to bodies in natural scenes.

The N190 is a body-sensitive ERP component that responds to images of human bodies in different poses. In natural settings, bodies vary in posture and appear within complex, cluttered environments, frequently with other people. In many studies, however, such variability is absent.

Sensitivity to face animacy and inversion in childhood: Evidence from EEG data.

Adults exhibit relative behavioral difficulties in processing inanimate, artificial faces compared to real human faces, with implications for using artificial faces in research and designing artificial social agents. However, the developmental trajectory of inanimate face perception is unknown. To address this gap, we used electroencephalography to investigate inanimate faces processing in cross-sectional groups of 5-10-year-old children and adults.

Neural sensitivity to natural image statistics changes during middle childhood.

Natural images have properties that adults' behavioral and neural responses are sensitive to, but the development of this sensitivity is not clear. Behaviorally, children acquire adult-like sensitivity to natural image statistics during middle childhood (Ellemberg et al., 2012), but infants exhibit sensitivity to deviations of natural image structure (Balas & Woods, 2014).

Children are sensitive to mutual information in intermediate-complexity face and non-face features.

Understanding developmental changes in children's use of specific visual information for recognizing object categories is essential for understanding how experience shapes recognition. Research on the development of face recognition has focused on children's use of low-level information (e.g.

Neural Sensitivity to Mutual Information in Intermediate-Complexity Face Features Changes during Childhood.

One way in which face recognition develops during infancy and childhood is with regard to the visual information that contributes most to recognition judgments. Adult face recognition depends on critical features spanning a hierarchy of complexity, including low-level, intermediate, and high-level visual information. To date, the development of adult-like information biases for face recognition has focused on low-level features, which are computationally well-defined but low in complexity, and high-level features, which are high in complexity, but not defined precisely.

Neural sensitivity to natural texture statistics in infancy.

During infancy, vision becomes tuned to environmental statistics. For example, infant face recognition "narrows" in response to the frequency of face categories in the visual world, inducing out-group effects that disadvantage other-race, other-species, and other-age face recognition. There are many other low-level statistical regularities in visual experience that infants may also become tuned to during this period.

The Impact of Face Inversion on Animacy Categorization.

Face animacy perception is categorical: Gradual changes in the real/artificial appearance of a face lead to nonlinear behavioral responses. Neural markers of face processing are also sensitive to face animacy, further suggesting that these are meaningful perceptual categories. Artificial faces also appear to be an "out-group" relative to real faces such that behavioral markers of expert-level processing are less evident with artificial faces than real ones.

School-age children's neural sensitivity to horizontal orientation energy in faces.

Face processing mechanisms are tuned to specific low-level features including mid-range spatial frequencies and horizontal orientation energy. Behaviorally, adult observers are more effective at face recognition tasks when these information channels are available. Neural responses to face images also reflect these information biases: Face-sensitive ERP components respond preferentially to face images that contain horizontal orientation energy.

Hometown size affects the processing of naturalistic face variability.

Face exposure during development determines adults' abilities to recognize faces and the information they use to process them. Individual differences in the face categories represented in the visual environment can lead to category-specific deficits for recognizing faces that are atypical of observer's experience (e.g.

Orientation biases for facial emotion recognition during childhood and adulthood.

Facial emotion recognition develops slowly, with continuing changes in performance observable up to 10 years of age and beyond. In the current study, we chose to examine how the use of specific low-level visual features for emotion recognition may change during childhood. Adults exhibit information biases for face recognition; specific spatial frequency and orientation sub-bands make a larger contribution to recognition than others.

A face detection bias for horizontal orientations develops in middle childhood.

Faces are complex stimuli that can be described via intuitive facial features like the eyes, nose, and mouth, "configural" features like the distances between facial landmarks, and features that correspond to computations performed in the early visual system (e.g., oriented edges).

N170 face specificity and face memory depend on hometown size.

Face recognition depends on visual experience in a number of different ways. Infrequent exposure to faces belonging to categories defined by species, age, or race can lead to diminished memory for and discrimination between members of those categories relative to faces belonging to categories that dominate an observer's environment. Early visual impairment can also have long-lasting and broad effects on face discrimination - just a few months of visual impairment due to congenital cataracts can lead to diminished discrimination between faces that differ in their configuration, for example (Le Grand et al.

Detecting personal familiarity depends on static frames in "thin slices" of behavior.

Brief glimpses of nonverbal behavior (or "thin slices") offer ample visual information to make reliable judgments about individuals. Previous work has largely focused on the personality characteristics and traits of individuals; however, the nature of dyadic relationships (strangers, lovers, or friends) can also be determined (Ambady & Gray, Journal of Personality and Social Psychology, 83, 947-961 2002). Judgments from thin slices are known to be accurate, but the motion features supporting accurate performance are unknown.

Reflexive orienting in response to short- and long-duration gaze cues in young, young-old, and old-old adults.

Shifting visual focus on the basis of the perceived gaze direction of another person is one form of joint attention. In the present study, we investigated whether this socially relevant form of orienting is reflexive and whether it is influenced by age. Green and Woldorff (Cognition 122:96-101, 2012) argued that rapid cueing effects (i.

Timing of reflexive visuospatial orienting in young, young-old, and old-old adults.

This study examined adult age differences in reflexive orienting to two types of uninformative spatial cues: central arrows and peripheral onsets. In two experiments using a Posner cuing task, young adults (ages 18-28 years), young-old adults (60-74 years), and old-old adults (75-92 years) responded to targets that were preceded 100-1,000 ms earlier by a central arrow or a peripheral abrupt onset. In Experiment 1, the cue remained present upon target onset.

Spatial distribution of attentional inhibition is not altered in healthy aging.

Inhibition of return (IOR) is a phenomenon of attentional orienting that is indexed by slower responses to targets presented at previously attended locations. The purpose of this study was to examine adult age differences in the distribution of IOR to multiple locations. In three experiments, young adults (ages 18-30 years) and older adults (ages 60-87 years) completed an IOR task that varied in the number of simultaneous onset cues (one to seven) and the number of display locations (four or eight).

The emotional blink: adult age differences in visual attention to emotional information.

To assess age differences in attention-emotion interactions, the authors asked young adults (ages 18-33 years) and older adults (ages 60-80 years) to identify target words in a rapid serial visual presentation (RSVP) task. The second of two target words was neutral or emotional in content (positive in Experiment 1, negative in Experiment 2). In general, the ability to identify targets from a word stream declined with age.

Adult age differences in attention to semantic context.

In three experiments age differences in attention to semantic context were examined. The performance of younger adults (ages 18-29 years) and older adults (ages 60-79 years) on a semantic priming task indicated that both age groups could use information regarding the probability that a prime and target would be related to flexibly anticipate the target category given the prime word (Experiment 1). The timing by which target expectancies were reflected in reaction time performance was delayed for older adults as compared to younger adults, but only when the target was expected to be semantically unrelated to the prime word (Experiment 2).

Aging and temporal patterns of inhibition of return.

Inhibition of return (IOR), an inhibitory component of spatial attention that is thought to bias visual search toward novel locations, is considered relatively well preserved with normal aging. We conducted two experiments to assess age-related changes in the temporal pattern of IOR. Inhibitory effects, which were strongly reflected in the performance of both younger adults (ages 18-34 years) and older adults (ages 60-79 years), diminished over a period of 5 s.