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PubMed1992

Recognition times for rotated normal and "Thatcher" faces.

To test whether face recognition is more disrupted by inversion than is the recognition of nonface stimuli and that an inverted Thatcher face is much less likely to be noticed as different than an upright one, reaction times were measured for recognizing "normal" and "abnormal" (Thatcher) faces (created by inverting the eyes and mouth relative to the rest of the face) presented at six orientation angles from upright. Over-all, reaction time of 22 students increased monotonically as faces were rotated away from upright; however, the orientation effect was essentially the same for both types of faces, indicating processing of faces is not qualitatively different from the processing of other types of stimuli. These data allow the inference that the subjects mentally rotated the internal features of eyes and mouth to upright and then judged whether the face was normal or abnormal.

Face↗
PubMed2000

Discriminating the sex of faces by 6- and 8-mo.-old infants.

The goal of this study was to ascertain at what age infants could discriminate male and female faces using only the internal features of the face. The habituation-dishabituation technique was used to estimate infants' discrimination between male and female faces. Analysis showed that 8-mo.-old infants discriminated female and male faces, whereas 6-mo.-old infants did not, but showed an asymmetry in discrimination. 6-mo.-old infants who were habituated to the female face fixated consistently longer on the novel male face in test trials, so sex discrimination was complete but not observed after habituation to male faces. Data are discussed in relation to the role of experience in face discrimination.

Discrimination Learning↗
PubMed2003

Practice and incentive motivation in recognition of inverted faces.

In each of three experiments, participants received successive daily practice sessions on the task of recognizing inverted faces. In all practice sessions, an initial study series of 25 inverted faces was followed immediately by a test series of 17 pairs of inverted faces. Each test pair comprised a face from the study series and a new face. Completely new sets of faces were used in each session. Recognition of inverted faces did not improve across sessions in Exp. 1 but did improve in Exps. 2 and 3. Unlike Exp. 1, Exps. 2 and 3 employed an explicit incentive for improved performance. These results show that sufficiently motivated participants can become quite proficient at recognizing inverted faces. Implications of the results for the role of expertise at recognition in producing the inversion effect are discussed.

Adult↗
PubMed1994

Detail, proportion, and foci among face receptive fields of climbing fiber responses in the cat cerebellum.

This paper reports a theoretical analysis of the transformation from a tactile stimulus of the face to climbing fiber responses in three regions of the cat cerebellum. The database consisted of climbing fiber receptive fields on the face from 75 responses from the anterior lobe, 33 responses from the paramedian lobule (PML), and 52 responses from the crus IIp of the anesthetized cat. The receptive fields were similar in being composed of discrete areas on the skin, or skin compartments. The regional differences in the configurations of the receptive fields were reflected in which compartments most often combined to form receptive fields. Each region had a distinct pattern of the preponderance of skin compartments that combined to form receptive fields, and yet the preponderant compartments were all chosen from one composite set of compartments that applied to all three regions. The climbing fiber representation of the face differed over the three regions (1) in the parts of the face that were represented; (2) in the frequency with which certain areas were included in the receptive fields; and (3) in the details of the face that could be distinguished by differing ensembles of climbing fiber responses. The majority of the climbing fiber receptive fields from either the anterior lobe or the crus IIp were unique to the region, whereas the majority of the receptive fields of responses from the PML were encountered in one or both of the other regions. Overlapping all face receptive fields from each of the three regions revealed that the receptive fields were differentially focused on or around the cornea, nose, or chin. In the anterior lobe, the face receptive fields mainly included the chin (43%) and the glabrous tip of the nose (40%), but few included the cornea (1%). In the PML, the receptive fields included the cornea (24%) and the chin (58%), but none included the nose. In the crus IIp, the cornea was included in the greatest number (37%) of receptive fields, whereas the nose and the chin were included equally (24%). The different sets of climbing fiber receptive fields in each of the three regions afforded the regions differing abilities to distinguish among complex patterns of stimuli, depending on the portion of the face stimulated.

Afferent Pathways↗
PubMed2005

Verbal facilitation of face recognition.

We examined the effects of verbally describing a face on face memory, as assessed in an old/new recognition task. Experiment 1 established that describing faces facilitated their later recognition. In Experiment 2, we argue that verbalization facilitated the recognition of faces that had been previously described, but not of faces intermingled with the described faces. In Experiment 3, the participants described (or did not, in the control condition) either differences or similarities between pairs of faces. Verbal facilitation was equivalent for both types of descriptions. Finally, in Experiment 4, the participants were instructed to generate either holistic or featural descriptors. Verbal facilitation was equivalent for both types of descriptors. We discuss these findings in terms of the nature of the verbalization that benefits face recognition.

Adolescent↗
PubMed2006

Recognizing distinctive faces: a hybrid-similarity exemplar model account.

In recognition memory experiments, Nosofsky and Zaki (2003) found that adding discrete distinctive features to continuous-dimension color stimuli helped participants to identify old items as old (the old-item distinctiveness effect), as well as to identify new items as new. The present study tests the extent to which these results generalize to the domain of face recognition. Two experiments were conducted, one using artificial faces and one using natural faces. Artificial faces were used to test memory for faces with discrete distinctive features while controlling the similarity of the faces themselves on more continuous dimensions. The natural-face experiment used the faces of 40 bald men categorized into three groups (typical, isolated, and distinctive) based on experimental ratings of distinctiveness. In both experiments, there were strong effects of the distinctive features on recognition performance. The data were accounted for reasonably well by a hybrid-similarity version of an exemplar recognition model (Nosofsky and Zaki, 2003), which includes a feature-matching mechanism that can provide boosts to an item's self-similarity.

Face↗
PubMed2006

Memory conjunction errors for realistic faces are consistent with configural processing.

Conjunction faces are formed from feature sets learned across different faces. In previous studies, false alarms ("old" responses) to conjunctions have been very high, approaching hits to old faces; this is surprising, because, perceptually, upright faces are processed configurally, with strong integration of parts into the whole. We test the idea that the atypical reliance on unrelated parts could be due to using unnatural line drawings as stimuli, and to forming conjunctions across external features (e.g., hair) and internal features (e.g., eyes, mouth). We used realistic face stimuli and conjunctions made entirely from internal features. Results were, as expected, consistent with configural processing for upright faces (hits to old faces much greater than FA to conjunctions) and not for inverted faces (hits to old = FA to conjunctions).

Association Learning↗
PubMed2002

Face recognition by hand.

We investigated participants' ability to identify and represent faces by hand. In Experiment 1, participants proved surprisingly capable of identifying unfamiliar live human faces using only their sense of touch. To evaluate the contribution of geometric and material information more directly, we biased participants toward encoding faces more in terms of geometric than material properties, by varying the exploration condition. When participants explored the faces both visually and tactually, identification accuracy did not improve relative to touch alone. When participants explored masks of the faces, thereby eliminating material cues, matching accuracy declined substantially relative to tactual identification of live faces. In Experiment 2, we explored intersensory transfer of face information between vision and touch. The findings are discussed in terms of their relevance to haptic object processing and to the face-processing literature in general.

Adolescent↗
PubMed1998

Prime time advertisements: repetition priming from faces seen on subject recruitment posters.

Repetition priming is defined as a gain in item recognition after previous exposure. Repetition priming of face recognition has been shown to last for several months, despite contamination by everyday exposure to both experimental and control faces in the interval. Here we show that gains in face recognition in the laboratory are found from faces initially seen in a rather different context--on subject recruitment posters, even when the advertisements make no specific mention of experiments involving face recognition. The priming was greatest when identical pictures were shown in the posters and in the test phase, although different views of faces did give significant priming in one study. Follow-up studies revealed poor explicit memory for the faces shown on the posters. The results of these experiments are used to develop a model in which repetition priming reflects the process of updating representations of familiar faces.

Adult↗
PubMed1999

Age differences in accuracy and choosing in eyewitness identification and face recognition.

Studies of aging and face recognition show age-related increases in false recognitions of new faces. To explore implications of this false alarm effect, we had young and senior adults perform (1) three eye-witness identification tasks, using both target present and target absent lineups, and (2) and old/new recognition task in which a study list of faces was followed by a test including old and new faces, along with conjunctions of old faces. Compared with the young, seniors had lower accuracy and higher choosing rates on the lineups, and they also falsely recognized more new faces on the recognition test. However, after screening for perceptual processing deficits, there was no age difference in false recognition of conjunctions, or in discriminating old faces from conjunctions. We conclude that the false alarm effect generalizes to lineup identification, but does not extend to conjunction faces. The findings are consistent with age-related deficits in recollection of context and relative age invariance in perceptual integrative processes underlying the experience of familiarity.

Adolescent↗
PubMed2005

The influence of processing objectives on the perception of faces: an ERP study of race and gender perception.

In two experiments, event-related potentials were used to examine the effects of attentional focus on the processing of race and gender cues from faces. When faces were still the focal stimuli, the processing of the faces at a level deeper than the social category by requiring a personality judgment resulted in early attention to race and gender, with race effects as early as 120 msec. This time course corresponds closely to those in past studies in which participants explicitly attended to target race and gender (Ito & Urland, 2003). However, a similar processing goal, coupled with a more complex stimulus array, delayed social category effects until 190 msec, in accord with the effects of complexity on visual attention. In addition, the N170 typically linked with structural face encoding was modulated by target race, but not by gender, when faces were perceived in a homogenous context consisting only of faces. This suggests that when basic-level distinctions between faces and nonfaces are irrelevant, the mechanism previously associated only with structural encoding can also be sensitive to features used to differentiate among faces.

Adult↗
PubMed1999

[The effects of identity of facial expression and person on face recognition: a study using priming paradigm].

Three experiments investigated the effects of identity of facial expression and person of two successively presented faces on face recognition. In each experiment, a combination of a familiar/unfamiliar person with neutral/smile expression was presented. Four different groups of 8 or 12 undergraduates were asked to judge the facial expression or the familiarity of the second face. The results showed that reaction times in both judgments were shorter when the same person repeatedly appeared than when two different people were presented. This repetition effect was not affected by facial expression of the stimulus for expression judgments, while it depended on the expression and familiarity of the first and second faces for familiarity judgments. In facial expression judgments, reaction times to smile faces were shorter than those to the neutral faces, only when subjects were familiar with those faces. This facial expression effect appeared only when the identical familiar and smile person was repeatedly presented for familiarity judgments. These results suggested the interdependency between analysis of facial expression and that of person information in face recognition processes.

Adult↗
PubMed2006

Variables influencing memory over long periods of time for recently learned face-name pairs.

The ability to match faces with corresponding names was studied under various conditions involving encoding and retrieval. Twenty photographs of undergraduates were randomly paired with 20 common names. Experiment 1 presented the photographs for 10 s each, followed by either presentation of the names alone with the instruction to write face characteristics from memory or presentation of the photographs again with instructions to write from memory the names and anything unusual about the names themselves. Later retrieval was best for the former condition and was interpreted as showing that names could prime image representations of faces. Experiment 2 was a partial replication of Experiment 1 with retrieval measured over 7 weeks. These results showed that memories for face-name matches lasted several weeks. Also, consistent with Experiment 1, the number of reported initial face characteristics was highly predictive of matches between faces and names. These studies show the importance for later retrieval of forming and maintaining vivid images of faces even when the faces have no outstanding characteristics.

Adult↗
PubMed1987

Anthropometrics and art in the aesthetics of women's faces.

Attractiveness of the face is not an abstract conception but a quantitatively well-defined anatomic quality. Harmony, disharmony, and disproportion of the face depend on the quality of the relationships between individual measurements of the craniofacial complex. The statistical expression of this relationship is the proportion index. A proportionate face, one with its proportion indices located within the normal range (mean +/- 2 SD), is healthy but not necessarily attractive. In an attractive face the proportion indices are in an optimal relationship, statistically in the range of mean +/- 1 SD. The existence of such a range ensures the great variability possible even among attractive faces. Disproportion, or even mild disharmony in a sensitive area of the face (orbits, nose, lips), reduces the aesthetic quality of the face. Restoration of harmony demands correction of the disproportionate relationships, which is achieved by appropriate changes in the measurements. Norms of measurements and proportion indices found in attractive faces serve as guides in calculating changes. Ethnic differences in North American Caucasian women proved not to be of major concern when planning aesthetic correction.

Anthropometry↗
PubMed1981

Within-race and between-race recognition of transformed and untransformed faces.

Numerous studies have shown that people from one racial group experience difficulties in remembering the faces of people from other racial groups. Two experiments are reported that explore the phenomenon more fully by examining subjects' ability to recognize faces transformed slightly in pose between study and test. Published work shows that white subjects can recognize such transformed white faces as well as they identify untransformed faces. In the first experiment, it was shown that white subjects were unable to recognize transformed black faces. The second experiment, following the pilot study, investigated recognition of both black and white, transformed and untransformed faces by Europeans and Africans. This study revealed that people from one racial group are particularly disadvantaged in recognizing other-race faces that have undergone transformation. The results are discussed in relation to learning approaches to face memory.

Adult↗
PubMed1977

When face recognition fails.

Two studies investigated recognition of pictures of faces, focusing on the effects of changes in appearance of the face from presentation to test and type of processing or encoding. Experiment 1 demonstrated that (a) previously seen faces changed in pose and facial expression were discriminated from "new" faces essentially as well as pictures identical at presentation and test; (b) major changes in the appearance of a face ("disguises") reduced recognition almost to the level of chance; and (c) subjects encoding faces in terms of personality characteristics showed better recognition performance than subjects whose processing was based on physical, facial features. Experiment 2 expanded on result (b), utilizing photographs with systematic variations in pose and in the presence/absence of glasses, wig, and beard. The design required subjects to learn names for target faces and then to identify those targets in a series of test photographs. The manipulation of pose and disguising features produced effects on probability of identification that were orderly and dramatic in magnitude. Simple changes in appearance can effectively interfere with recognition of faces.

Attention↗
PubMedDate not supplied

Baiting the cross-face nerve graft with temporary hypoglossal hookup.

BACKGROUND: Cross-face nerve grafting yields inconsistent neural regeneration, and methods that promote more robust axonal traversing of the graft would expand the indications for this procedure. OBJECTIVE: To test the hypothesis that hooking a cross-face nerve graft distally to a source of denervated muscle, rather than leaving it in the subcutaneous space, would positively affect neural ingrowth across the graft, based on elaboration of neurotrophins from the musculature. METHODS: Twenty-four rats underwent cross-face nerve grafting in which the right facial nerve buccal branch was transected and coapted to the graft. The graft was placed across the neck and into the left side of the face. The distal end of the graft was placed either in the left subcutaneous space, coapted to the marginal mandibular branch of the left facial nerve, or coapted to the distal stump of the transected left hypoglossal nerve. Eight control animals underwent right buccal branch transection and placement of a cross-face nerve graft without any proximal and distal hookup. After 12 weeks, all experimental groups underwent hookup of the distal nerve graft to the left facial nerve buccal branch. Vibrissal function was assessed during the ensuing 12 weeks, and then the graft was harvested for histomorphometric analysis. RESULTS: After 12 weeks, there was a significant difference in axon counts between the group coapted distally to the tongue (hypoglossal hookup) and that coapted to the facial musculature (marginal hookup). Twelve weeks later, after distal cross-face nerve graft hookup, this difference was not statistically significant, although the hypoglossally baited group demonstrated statistically significantly greater fiber maturity. Recovery of vibrissal movement did not differ among treatment groups. CONCLUSION: Baiting the cross-face nerve graft via temporary hookup to the distal hypoglossal nerve and tongue musculature appears to improve nerve ingrowth through a nerve graft across the face, although a corresponding improvement in facial muscle function was not observed.

Animals↗
PubMed2002

Age-related differences in the medial temporal lobe responses to emotional faces as revealed by fMRI.

Age-related differences involved in the neural substrates of emotional face perception were investigated in young and old healthy volunteers. The subjects were scanned using functional magnetic resonance imaging while they were judging the gender of faces with negative, positive, or neutral emotional valence. The results showed that both the predominant activation in young subjects and reduced activity in old subjects contributed to a significant age difference in the left amygdala during the perception of negative faces. Activity in the right parahippocampal gyrus during the perception of positive faces diminished with advancing age. Neural activity in the angular gyrus and lingual gyrus of the right hemisphere was reduced in the old subjects during the perception of positive faces. There was no region where old subjects had greater activity than young subjects during the task. In old subjects, the overall activity in the right hippocampus during the task correlated negatively with age, whereas the activity in the right parahippocampal gyrus correlated positively with neuropsychological performance. There was no significant correlation between subjects' characteristics and signal change in young subjects. These results indicate the age-associated vulnerability of the medial temporal lobe structures including the amygdala, hippocampus, and parahippocampal gyrus during face perception. The dissociation with reduced activity in the left amygdala and the right parahippocampal gyrus may suggest that aging differentially affects neural responses to faces with negative or positive emotional valence. The parieto-occipital lobe, which has been found to be involved in face processing, also showed a functional decline associated with aging.

Adult↗