Vulnerability to disease is associated with a domain‐specific preference for symmetrical faces relative to symmetrical non‐face stimuli

Two experiments tested the hypothesis that the accessibility of disease concerns would be associated with a preference for faces high in symmetry, a cue to good health and pathogen resistance. Disease concerns (perceived vulnerability to disease) were measured as an individual difference in Experiment 1 and were situationally primed in Experiment 2. Across both studies, heightened disease sensitivity predicted a preference for symmetrical faces. Importantly, this increased preference for symmetrical faces when disease threats were salient did not generalize to non‐face stimuli. These results suggest a domain‐specific preference for symmetry in human faces, an adaptive response due to the ability of faces to signal resistance to infectious diseases in individuals and situations where disease is a salient threat. Copyright © 2011 John Wiley & Sons, Ltd.     

Face processing at birth: a Thatcher illusion study

The present study was aimed at exploring newborns’ ability to recognize configural changes within real face images by testing newborns’ sensitivity to the Thatcher illusion. Using the habituation procedure, newborns’ ability to discriminate between an unaltered face image and the same face with the eyes and the mouth 180° rotated (i.e. thatcherized) was investigated. Newborns were able to discriminate an unaltered from the thatcherized version of the same face when stimuli were presented in the canonical upright orientation (Experiment 1), but failed to discriminate the same stimuli when they were presented upside‐down (Experiment 2). The results indicate that sensitivity to fine spatial information (defined as second‐order relational information) in processing upright faces is already present at birth.     

The movement of internal facial features elicits 7 to 8‐month‐old infants' preference for face patterns

A preference for static face patterns is observed in newborns and disappears around 3 months after birth. A previous study has demonstrated that 5‐month‐old infants prefer schematic faces only when the internal features are moving, suggesting that face‐specific movement enhances infants' preference. The present study investigates the facilitative effect of the movement of internal facial features on infants' preference. To examine infants' preference, we used animated face patterns consisting of a head‐shaped contour and three disk blobs. The inner blobs expanded and contracted to represent the opening and closing of the eyes and mouth, and were constrained to open and close only in a biologically possible vertical direction resembling the facial muscle structure. We compared infants' preferential looking time for this vertically moving (VM) face pattern with their looking time for a horizontally moving (HM) face pattern in which blobs transformed at the same speed in a biologically impossible, horizontal direction. In Experiment 1, 7 to 8‐month‐olds preferred the VM to the HM, but 5 to 6‐month‐olds did not. However, the preference was diminished in both cases when the moving face patterns were presented without contour (Experiment 2). Our results suggest that internal facial features with vertical movements promote face preference in 7 to 8‐month‐olds. Copyright © 2011 John Wiley & Sons, Ltd.     

Impaired face recognition does not preclude intact whole face perception

We studied intact and impaired processes in a prosopagnosic patient (RP). In Experiment 1, RP showed an inversion superiority effect with both faces and objects, with better performance when stimuli were presented upside down than in normal upright orientation. In Experiment 2, we studied the effect of face configuration directly by comparing matching performance with normal vs. scrambled faces. RP was worse with normal than with scrambled faces, whereas normal controls showed an advantage of a good face context. In Experiment 3, RP showed interference from external face features on the evaluation of internal face features. These results indicate, first, that although RP is impaired in face recognition and face matching, he does still encode the whole face rather than relying completely on parts-based procedures. Second, RP has a deficit at the level of the configural processes involved in finding subtle differences between individual faces, as his performance is worse when presented with a normal face configuration than with scrambled or inverted faces.     

Face‐specific configural processing of relational information

Face processing relies on configural processing, which is thought to be particularly disrupted by inversion. We compared inversion effects in recognition experiments for three types of stimuli, using faces (Experiment 1) and houses (Experiment 2). Stimuli varied by their colour only (colour), by the spatial relations between components (relational), or by the components themselves (eyes, mouths, doors). For faces, relational versions revealed strong inversion effects, component versions moderate, and colour versions no inversion effect. Recognition of houses revealed no inversion effects at all. We suggest that the inversion effects observed for faces in the component condition are due to relational changes, which must accompany any change in components. This proposal may account for the rather inconsistent effects of inversion reported in the literature. Furthermore, we suggest configural processing seems to be somehow face‐specific.     

The own‐age face recognition bias is task dependent

The own‐age bias (OAB) in face recognition (more accurate recognition of own‐age than other‐age faces) is robust among young adults but not older adults. We investigated the OAB under two different task conditions. In Experiment 1 young and older adults (who reported more recent experience with own than other‐age faces) completed a match‐to‐sample task with young and older adult faces; only young adults showed an OAB. In Experiment 2 young and older adults completed an identity detection task in which we manipulated the identity strength of target and distracter identities by morphing each face with an average face in 20% steps. Accuracy increased with identity strength and facial age influenced older adults' (but not younger adults') strategy, but there was no evidence of an OAB. Collectively, these results suggest that the OAB depends on task demands and may be absent when searching for one identity.     

Development of category formation for faces differing by age in 9‐ to 12‐month‐olds: An effect of experience with infant faces

We examined category formation for faces differing in age in 9‐ and 12‐month‐olds, and the influence of exposure to infant faces on such ability. Infants were familiarized with adult or infant faces, and then tested with a novel exemplar from the familiarized category paired with a novel exemplar from a novel category (Experiment 1). Both age groups formed discrete categories of adult and infant faces, but exposure to infant faces in everyday life did not modulate performance. The same task was conducted with child versus infant faces (Experiment 2). Whereas 9‐month‐olds preferred infant faces after familiarization with child faces, but not child faces after familiarization with infant faces, 12‐month‐olds formed discrete categories of child and infant faces. Moreover, more exposure to infant faces correlated with higher novel category preference scores when infants were familiarized with infant faces in 12‐month‐olds, but not 9‐month‐olds. The 9‐month‐old asymmetry did not reflect spontaneous preference for infant over child faces (Experiment 3). These findings indicate that 9‐ and 12‐month‐olds can form age‐based categories of faces. The ability of 12‐month‐olds to form separate child and infant categories suggests that they have a more exclusive representation of face age, one that may be influenced by prior experience with infant faces.     

Two‐ to three‐month‐old infants prefer moving face patterns to moving top‐heavy patterns

Newborn infants prefer face‐like patterns over non‐face‐like patterns. This preference is explained by newborns' preference for a “top‐heavy” configuration, that is, for geometric patterns that have more elements in the upper part than in the lower part of the configuration (Simion, Valenza, Macchi Cassia, Turati, & Umiltà, 2002). However, for 3‐month‐old infants, face preference cannot be explained only by a preference for “top‐heaviness” because they prefer veridical face images over top‐heavy images. The present study used geometric patterns to investigate whether 2‐ to 3‐month‐old infants' preference for face patterns exceeds their preference for top‐heavy configurations. In Experiment 1, we revealed that the infants preferred the face pattern to the top‐heavy pattern only when the internal elements of the patterns were presented with face‐like movements. This facilitative effect of internal movement was observed again in Experiment 2, in which the patterns were presented with non‐face‐like movements. These results suggest that 2‐ to 3‐month‐olds' preference for geometric face patterns is greater than their preference for top‐heavy patterns only when aided by the movement of internal elements.     

Individuation training with other‐race faces reduces preschoolers’ implicit racial bias: a link between perceptual and social representation of faces in children

The present study examined whether perceptual individuation training with other‐race faces could reduce preschool children's implicit racial bias. We used an ‘angry = outgroup’ paradigm to measure Chinese children's implicit racial bias against African individuals before and after training. In Experiment 1, children between 4 and 6 years were presented with angry or happy racially ambiguous faces that were morphed between Chinese and African faces. Initially, Chinese children demonstrated implicit racial bias: they categorized happy racially ambiguous faces as own‐race (Chinese) and angry racially ambiguous faces as other‐race (African). Then, the children participated in a training session where they learned to individuate African faces. Children's implicit racial bias was significantly reduced after training relative to that before training. Experiment 2 used the same procedure as Experiment 1, except that Chinese children were trained with own‐race Chinese faces. These children did not display a significant reduction in implicit racial bias. Our results demonstrate that early implicit racial bias can be reduced by presenting children with other‐race face individuation training, and support a linkage between perceptual and social representations of face information in children.     

Infant preference for female faces occurs for same‐ but not other‐race faces

There has been a recent surge of interest in the question of how infants respond to the social attributes of race and gender information in faces. This work has demonstrated that by 3 months of age, infants will respond preferentially to same‐race faces and faces depicting the gender of the primary caregiver. In the current study, we investigated emergence of the female face preference for same‐ versus other‐race faces to examine whether the determinants of preference for face gender and race are independent or interactive in young infants. In Expt 1, 3‐month‐old Caucasian infants displayed a preference for female over male faces when the faces were Caucasian, but not when the faces were Asian. In Expt 2, new‐born Caucasian infants did not demonstrate a preference for female over male faces for Caucasian faces. The results are discussed in terms of a face prototype that becomes progressively tuned as it is structured by the interaction of the gender and race of faces that are experienced during early development.     

Ingroup and outgroup differences in face detection

Humans show improved recognition for faces from their own social group relative to faces from another social group. Yet before faces can be recognized, they must first be detected in the visual field. Here, we tested whether humans also show an ingroup bias at the earliest stage of face processing – the point at which the presence of a face is first detected. To this end, we measured viewers' ability to detect ingroup (Black and White) and outgroup faces (Asian, Black, and White) in everyday scenes. Ingroup faces were detected with greater speed and accuracy relative to outgroup faces (Experiment 1). Removing face hue impaired detection generally, but the ingroup detection advantage was undiminished (Experiment 2). This same pattern was replicated by a detection algorithm using face templates derived from human data (Experiment 3). These findings demonstrate that the established ingroup bias in face processing can extend to the early process of detection. This effect is ‘colour blind’, in the sense that group membership effects are independent of general effects of image hue. Moreover, it can be captured by tuning visual templates to reflect the statistics of observers' social experience. We conclude that group bias in face detection is both a visual and a social phenomenon.     

Sensitivity to First‐Order Relations of Facial Elements in Infant Rhesus Macaques

Faces are visually attractive to both human and nonhuman primates. Human neonates are thought to have a broad template for faces at birth and prefer face‐like to non‐face‐like stimuli. To better compare developmental trajectories of face processing phylogenetically, here, we investigated preferences for face‐like stimuli in infant rhesus macaques using photographs of real faces. We presented infant macaques aged 15–25 days with human, macaque and abstract faces with both normal and linear arrangements of facial features and measured infants' gaze durations, number of fixations and latency to look to each face using eye‐tracking technology. There was an overall preference for normal over linear facial arrangements for abstract and monkey faces but not human faces. Moreover, infant macaques looked less at monkey faces than at abstract or human faces. These results suggest that species and facial configurations affect face processing in infant macaques, and we discuss potential explanations for these findings. Further, carefully controlled studies are required to ascertain whether infant macaques' face template can be considered as broad as human infants' face template. Copyright © 2013 John Wiley & Sons, Ltd.     

The neural correlates of processing newborn and adult faces in 3‐year‐old children

The current study examines the processing of upright and inverted faces in 3‐year‐old children (n = 35). Event‐related potentials (ERPs) were recorded during a passive looking paradigm including adult and newborn face stimuli. We observed three face‐sensitive components, the P1, the N170 and the P400. Inverted faces elicited shorter P1 latency and larger P400 amplitude. P1 and N170 amplitudes were larger for adult faces. To examine the role of experience in the development of face processing, the processing of adult and newborn faces was compared for children with a younger sibling (n = 23) and children without a younger sibling (n = 12). Age of sibling at test correlated negatively with P1 amplitude for adult and newborn faces. This may indicate more efficient processing of different face ages in children with a younger sibling and potentially reflects a more flexible face representation.     

The flip side of the other‐race coin: They all look different to me

Poorer recognition of other‐race faces than own‐races faces has been attributed to a problem of discrimination (i.e., telling faces apart). The conclusion that ‘they all look the same to me' is based on studies measuring the perception/memory of highly controlled stimuli, typically involving only one or two images of each identity. We hypothesized that such studies underestimate the challenge involved in recognizing other‐race faces because in the real world, an individual's appearance varies in a number of ways (e.g., lighting, expression, hairstyle), reducing the utility of relying on pictorial cues to identity. In two experiments, Caucasian and East Asian participants completed a perceptual sorting task in which they were asked to sort 40 photographs of two unfamiliar identities into piles such that each pile contained all photographs of a single identity. Participants perceived more identities when sorting other‐race faces than own‐race faces, both when sorting celebrity (Experiment 1) and non‐celebrity (Experiment 2) faces, suggesting that in the real world, ‘they all look different to me'. We discuss these results in the light of models in which each identity is represented as a region in a multidimensional face space; we argue that this region is smaller for other‐race than own‐race faces.     

Brain activation during upright and inverted encoding of own‐ and other‐age faces: ERP evidence for an own‐age bias

We investigated the neural processing underlying own‐age versus other‐age faces among 5‐year‐old children and adults, as well as the effect of orientation on face processing. Upright and inverted faces of 5‐year‐old children, adults, and elderly adults (> 75 years of age) were presented to participants while ERPs and eye tracking patterns were recorded concurrently. We found evidence for an own‐age bias in children, as well as for predicted delayed latencies and larger amplitudes for inverted faces, which replicates earlier findings. Finally, we extend recent reports about an expert‐sensitive component (P2) to other‐race faces to account for similar effects in regard to other‐age faces. We conclude that differences in neural activity are strongly related to the amount and quality of experience that participants have with faces of various ages. Effects of orientation are discussed in relation to the holistic hypothesis and recent data that compromise this view.     

More Inaccurate But Not More Biased: Anxiety During Encoding Impairs Face Recognition Accuracy But Does Not Moderate the Own‐Ethnicity Bias

Heightened state anxiety can have a deleterious impact on memory for faces. In this paper we investigated whether anxiety: (i) moderates the own‐ethnicity bias (OEB) and (ii) impairs face recognition accuracy at the encoding or retrieval phase of an OEB face‐recognition task. Using a typical OEB task, anxiety was induced during encoding and retrieval in Experiment 1, but only during retrieval in Experiment 2. An OEB was found in both experiments, but anxiety did not moderate the OEB in either experiment. In Experiment 1, anxious participants were poorer at face recognition for both own‐ and other‐ethnicity faces. In Experiment 2 anxiety did not impair face recognition. Together, these studies suggest that anxiety impaired participants' encoding, but not retrieval, of faces. The implications of these findings are discussed. Copyright © 2015 John Wiley & Sons, Ltd.     

Sensitivity to auditory‐tactile colocation in early infancy

An ability to detect the common location of multisensory stimulation is essential for us to perceive a coherent environment, to represent the interface between the body and the external world, and to act on sensory information. Regarding the tactile environment “at hand”, we need to represent somatosensory stimuli impinging on the skin surface in the same spatial reference frame as distal stimuli, such as those transduced by vision and audition. Across two experiments we investigated whether 6‐ (n = 14; Experiment 1) and 4‐month‐old (n = 14; Experiment 2) infants were sensitive to the colocation of tactile and auditory signals delivered to the hands. We recorded infants’ visual preferences for spatially congruent and incongruent auditory‐tactile events delivered to their hands. At 6 months, infants looked longer toward incongruent stimuli, whilst at 4 months infants looked longer toward congruent stimuli. Thus, even from 4 months of age, infants are sensitive to the colocation of simultaneously presented auditory and tactile stimuli. We conclude that 4‐ and 6‐month‐old infants can represent auditory and tactile stimuli in a common spatial frame of reference. We explain the age‐wise shift in infants’ preferences from congruent to incongruent in terms of an increased preference for novel crossmodal spatial relations based on the accumulation of experience. A comparison of looking preferences across the congruent and incongruent conditions with a unisensory control condition indicates that the ability to perceive auditory‐tactile colocation is based on a crossmodal rather than a supramodal spatial code by 6 months of age at least.     

Is the face-perception system human-specific at birth?

The present study investigates the human-specificity of the orienting system that allows neonates to look preferentially at faces. Three experiments were carried out to determine whether the face-perception system that is present at birth is broad enough to include both human and nonhuman primate faces. The results demonstrate that the newborns did not show any spontaneous visual preference for the human face when presented simultaneously with a monkey face that shared the same features, configuration, and low-level perceptual properties (Experiment 1). The newborns were, however, able to discriminate between the 2 faces belonging to the 2 different species (Experiment 2). In Experiment 3, the newborns were found to prefer looking at an upright, compared with an inverted, monkey face, as they do for human faces. Overall, the results demonstrate that newborns perceive monkey and human faces in a similar way. These findings are consistent with the hypothesis that the system underlying face preference at birth is broad enough to bias newborns' attention toward both human and nonhuman primate faces.     

More than just another face in the crowd: superior detection of threatening facial expressions in children and adults

Threatening facial expressions can signal the approach of someone or something potentially dangerous. Past research has established that adults have an attentional bias for angry faces, visually detecting their presence more quickly than happy or neutral faces. Two new findings are reported here. First, evidence is presented that young children share this attentional bias. In five experiments, young children and adults were asked to find a picture of a target face among an array of eight distracter faces. Both age groups detected threat‐relevant faces – angry and frightened – more rapidly than non‐threat‐relevant faces (happy and sad). Second, evidence is presented that both adults and children have an attentional bias for negative stimuli overall. All negative faces were detected more quickly than positive ones in both age groups. As the first evidence that young children exhibit the same superior detection of threatening facial expressions as adults, this research provides important support for the existence of an evolved attentional bias for threatening stimuli.     

Dominance of texture over shape in facial identity processing is modulated by individual abilities

For face recognition, observers utilize both shape and texture information. Here, we investigated the relative diagnosticity of shape and texture for delayed matching of familiar and unfamiliar faces (Experiment 1) and identifying familiar and newly learned faces (Experiment 2). Within each familiarity condition, pairs of 3D‐captured faces were morphed selectively in either shape or texture in 20% steps, holding the respective other dimension constant. We also assessed participants’ individual face‐processing skills via the Bielefelder Famous Faces Test (BFFT), the Glasgow Face Matching Test, and the Cambridge Face Memory Test (CFMT). Using multilevel model analyses, we examined probabilities of same versus different responses (Experiment 1) and of original identity versus other/unknown identity responses (Experiment 2). Overall, texture was more diagnostic than shape for both delayed matching and identification, particularly so for familiar faces. On top of these overall effects, above‐average BFFT performance was associated with enhanced utilization of texture in both experiments. Furthermore, above‐average CFMT performance coincided with slightly reduced texture dominance in the delayed matching task (Experiment 1) and stronger sensitivity to morph‐based changes overall, that is irrespective of morph type, in the face identification task (Experiment 2). Our findings (1) show the disproportionate importance of texture information for processing familiar face identity and (2) provide further evidence that familiar and unfamiliar face identity perception are mediated by different underlying processes.