The importance of social factors is a matter of perception

Caucasian female faces were randomly assigned to participants' in- or out-group following false feedback on a personality inventory. Participants recognised in-group faces better than out-group faces, but they showed no evidence of category-contingent opposing aftereffects. We conclude that the explanatory power of social-cognitive models will be enhanced when they are integrated with models of perceptual expertise.     

The many faces of configural processing

Adults' expertise in recognizing faces has been attributed to configural processing. We distinguish three types of configural processing: detecting the first-order relations that define faces (i.e. two eyes above a nose and mouth), holistic processing (glueing the features together into a gestalt), and processing second-order relations (i.e. the spacing among features). We provide evidence for their separability based on behavioral marker tasks, their sensitivity to experimental manipulations, and their patterns of development. We note that inversion affects each type of configural processing, not just sensitivity to second-order relations, and we review evidence on whether configural processing is unique to faces.     

Visual configural processing in adults born at extremely low birth weight

Being born at extremely low birth weight (ELBW; ≤1,000 g) is associated with enduring visual impairments. We tested for long‐term, higher order visual processing problems in the oldest known prospectively followed cohort of ELBW survivors. Configural processing (spacing among features of an object) was examined in 62 adults born at ELBW (M_age = 31.9 years) and 82 adults born at normal birth weight (NBW; ≥2,500 g: M_age = 32.5 years). Pairs of human faces, monkey faces, or houses were presented in a delayed match‐to‐sample task, where non‐matching stimuli differed only in the spacing of their features. Discrimination accuracy for each stimulus type was compared between birth weight groups, adjusting for neurosensory impairment, visual acuity, binocular fusion ability, IQ, and sex. Both groups were better able to discriminate human faces than monkey faces (p < .001). However, the ELBW group discriminated between human faces (p < .001), between monkey faces (p < .001), and to some degree, between houses (p < .06), more poorly than NBW control participants, suggesting a general deficit in perceptual processing. Human face discrimination was related to performance IQ (PIQ) across groups, but especially among ELBW survivors. Coding (a PIQ subtest) also predicted human face discrimination in ELBW survivors, consistent with previously reported links between visuo‐perceptive difficulties and regional slowing of cortical activity in individuals born preterm. Correlations with Coding suggested ELBW survivors may have used a feature‐matching approach to processing human faces. Future studies could examine brain‐based anatomical and functional evidence for altered face processing, as well as the social and memory consequences of face‐processing deficits in ELBW survivors.     

Finding an unfamiliar face in a line-up: Viewing multiple images of the target is beneficial on target-present trials but costly on target-absent trials

When viewing unfamiliar faces, photographs of the same person often are perceived as belonging to different people and photographs of different people as belonging to the same person. Identity matching of unfamiliar faces is especially challenging when the photographs are of a person whose ethnicity differs from that of the observer. In contrast, matching is trivial when viewing familiar faces, regardless of race. Viewing multiple images of an own-race target identity improves accuracy on a line-up task when the target is known to be present (Dowsett et al., 2016, Q J Exp Psychol, 69, 1), suggesting that exposure to within-person variability in appearance is key to face learning. Across three experiments, we show that viewing multiple images of a target identity also improves accuracy for other-race faces on target-present trials. However, viewing multiple images decreases accuracy (i.e., increases false alarms) on target-absent trials for both own- and other-race faces. We discuss the implications of our findings for models of face recognition and for forensic settings.     

Effects of normal and abnormal visual experience on the development of opposing aftereffects for upright and inverted faces

We used opposing figural aftereffects to investigate whether there are at least partially separable representations of upright and inverted faces in patients who missed early visual experience because of bilateral congenital cataracts (mean age at test 19.5 years). Visually normal adults and 10-year-olds were tested for comparison. Adults showed the expected opposing aftereffects for upright and inverted faces. Ten-year-olds showed an adultlike aftereffect for upright faces but, unlike the adult group, no aftereffect for inverted faces. Patients failed to show an aftereffect for either upright or inverted faces. Overall, the results suggest that early visual input is necessary for the later development of (at least partially) separable representations of upright and inverted faces, a developmental process that takes many years to reach an adult-like refinement.     

What aspects of face processing are impaired in developmental prosopagnosia?

Developmental prosopagnosia (DP) is a severe impairment in identifying faces that is present from early in life and that occurs despite no apparent brain damage and intact visual and intellectual function. Here, we investigated what aspects of face processing are impaired/spared in developmental prosopagnosia by examining a relatively large group of individuals with DP (n = 8) using an extensive battery of well-established tasks. The tasks included measures of sensitivity to global motion and to global form, detection that a stimulus is a face, determination of its sex, holistic face processing, processing of face identity based on features, contour, and the spacing of features, and judgments of attractiveness. The DP cases showed normal sensitivity to global motion and global form and performed normally on our tests of face detection and holistic processing. On the other tasks, many DP cases were impaired but there was no systematic pattern. At least half showed deficits in processing of facial identity based on either the outer contour or spacing of the internal features, and/or on judgments of attractiveness. Three of the eight were impaired in processing facial identify based on the shape of internal features. The results show that DP is a heterogeneous condition and that impairment in recognizing faces cannot be predicted by poor performance on any one measure of face processing.     

The effect of face orientation on holistic processing

Holistic processing, a hallmark of face processing, can be measured by the composite face effect: adults have difficulty recognising the top half of a face when it is aligned with a new bottom half, unless holistic processing is disrupted by misaligning the two halves. Like the recognition of facial identity, holistic processing is impaired when faces are inverted. To obtain a more refined measure of the influence of orientation on holistic face processing, we administered the composite face task to adults at each of seven orientations. In both experiment 1 (in which orientations were randomly intermixed) and experiment 2 (in which orientations were blocked), the composite face effect decreased linearly with rotation. We conclude that holistic processing is tuned to upright faces, diminishes as faces deviate from upright, and becomes insignificant once faces reach a sideways orientation. We propose a hierarchical model of face perception in which linear decreases in holistic processing underlie qualitative shifts in other aspects of face perception.     

Sleeper effects

Early experience preserves and refines many capabilities that emerge prenatally. Here we describe another role that it plays -- establishing the neural substrate for capabilities that emerge at a much later point in development. The evidence comes from sleeper effects: permanent deficits when early experience was absent in capabilities that normally emerge long after birth. We provide evidence of sleeper effects for three aspects of vision, based on our research with children who were deprived of early visual input by congenital cataracts: contrast sensitivity for mid and high spatial frequencies, holistic face processing, and the ability to recognize the identity of faces based on small differences in the spacing among facial features.     

Processes underlying the cross-race effect: an investigation of holistic, featural, and relational processing of own-race versus other-race faces

Adults are often better at recognising own-race than other-race faces. Unlike previous studies that reported an own-race advantage after administering a single test of either holistic processing or of featural and relational processing, we used a cross-over design and multiple tasks to assess differential processing of faces from a familiar race versus a less familiar race. Caucasian and Chinese adults performed four tasks, each with Caucasian and Chinese faces. Two tasks measured holistic processing: the composite face task and the part/whole task. Both tasks indicated holistic processing of own-race and other-race faces that did not differ in degree. Two tasks measured featural and relational processing: the Jane/Ling task, in which same/ different judgments were made about face pairs that differed in features of their spacing, and the scrambled/blurred task, in which test faces were scrambled (isolates memory for components) or blurred (isolates memory for relations). Both tasks provided evidence of an own-race advantage in both featural and relational processing. We conclude that even when adults process other-race faces holistically, other manifestations of an own-race advantage remain.     

The influence of postural emotion cues on implicit trait judgements

Perceptions of others’ traits (e.g., trustworthiness or dominance) are influenced by the emotion displayed on their face. For instance, the same individual appears more trustworthy when they express happiness than when they express anger. This overextension of emotional expressions has been shown with facial expression but whether this phenomenon also occurs when viewing postural expressions was unknown. We sought to examine how expressive behaviour of the body would influence judgements of traits and how sensitivity to this cue develops. In the context of a storybook, adults (N?=?35) and children (5 to 8 years old; N?=?60) selected one of two partners to help face a challenge. The challenges required either a trustworthy or dominant partner. Participants chose between a partner with an emotional (happy/angry) face and neutral body or one with a neutral face and emotional body. As predicted, happy facial expressions were preferred over neutral ones when selecting a trustworthy partner and angry postural expressions were preferred over neutral ones when selecting a dominant partner. Children’s performance was not adult-like on most tasks. The results demonstrate that emotional postural expressions can also influence judgments of others’ traits, but that postural influence on trait judgments develops throughout childhood.