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At least 1,099 records · Page 61Linked to original sources
PubMed1997

Face immersion increases vagal activity as assessed by heart rate variability.

We examined whether the diving reflex without breath-holding (face immersion alone) increases vagal activity, as determined by heart rate variability. A group of 15 men [mean age 20 (SD 3) years, height 172 (SD 5) cm, body mass 68 (SD 9) kg] performed 12 trials at various breathing frequencies (5, 10, 15, 20, 30 breaths x min(-1) and uncontrolled breath) with or without face immersion. The R-R intervals of the ECG and gas exchange variables were recorded during the 2 min of each trial. The subjects immersed their faces in 8 10 degrees C water while breathing through a short snorkel. The subject sat in the same position either with or without face immersion. The mean R-R interval (RRmean), standard deviations (SD[RR]) and coefficient of variance (CV[RR]) of the R-R interval were calculated from the R-R intervals during 30-120 s. The face immersion significantly increased SD(RR) and CV(RR) (P < 0.05), and increased RRmean (P < 0.05) at 20 breaths x min(-1). Face immersion itself had no effect on oxygen uptake, tidal volume, end-tidal O2 and CO2 partial pressures. The diving reflex without breath-holding increased the heart rate variability, indicating that face immersion alone increases vagal activity.

Adult↗
PubMed2004

Body orientation and face orientation: two factors controlling apes' behavior from humans.

A number of animal species have evolved the cognitive ability to detect when they are being watched by other individuals. Precisely what kind of information they use to make this determination is unknown. There is particular controversy in the case of the great apes because different studies report conflicting results. In experiment 1, we presented chimpanzees, orangutans, and bonobos with a situation in which they had to request food from a human observer who was in one of various attentional states. She either stared at the ape, faced the ape with her eyes closed, sat with her back towards the ape, or left the room. In experiment 2, we systematically crossed the observer's body and face orientation so that the observer could have her body and/or face oriented either towards or away from the subject. Results indicated that apes produced more behaviors when they were being watched. They did this not only on the basis of whether they could see the experimenter as a whole, but they were sensitive to her body and face orientation separately. These results suggest that body and face orientation encode two different types of information. Whereas face orientation encodes the observer's perceptual access, body orientation encodes the observer's disposition to transfer food. In contrast to the results on body and face orientation, only two of the tested subjects responded to the state of the observer's eyes.

Animals↗
PubMed1995

Categorical effects in the perception of faces.

These studies suggest categorical perception effects may be much more general than has commonly been believed and can occur in apparently similar ways at dramatically different levels of processing. To test the nature of individual face representations, a linear continuum of "morphed" faces was generated between individual exemplars of familiar faces. In separate categorization, discrimination and "better-likeness" tasks, subjects viewed pairs of faces from these continua. Subjects discriminate most accurately when face-pairs straddle apparent category boundaries; thus individual faces are perceived categorically. A high correlation is found between the familiarity of a face-pair and the magnitude of the categorization effect. Categorical perception therefore is not limited to low-level perceptual continua, but can occur at higher levels and may be acquired through experience as well.

Face↗
PubMed1985

Developmental changes in face processing: results from multidimensional scaling.

Multidimensional scaling procedures were used to investigate developmental changes in the ability to process previously unfamiliar faces. Eighty male subjects, aged 7, 9, 12, or adult, rated the similarity of pairs of faces. The faces were presented to subjects in either the upright or the inverted orientation. Multidimensional scaling analyses suggest that subjects of all ages use similar information in judging the similarity of faces. However, for upright faces, individual subjects under age 10 seem to use fewer features at a time. The results argue against a qualitative shift in face processing at age 10, and suggest that the improvement in face recognition ability noted at this age is due at least in part to an increased ability to consider more features simultaneously.

Adult↗
PubMed1984

Face touching in monkeys, apes and man evolutionary origins and cerebral asymmetry.

The evolution of face touching, i.e. the use of the hand to touch the individual's own face, was studied in monkeys, apes and man with the object of examining which hand is used and which part of the face is touched. Monkeys show little if any face touching. Gorillas, orang- utans and chimpanzees show face-touching comparable to man. Left-hand face touching was superior to right-hand touching for both apes and humans. One feature which distinguished humans from other apes was the frequency of chin touching, which is generally high for man. It has been suggested that emotions are expressed more intensely on the left side of the face and it was thought that the left hand is used by the right hemisphere as a special pointer to heighten the effect of this.

Animals↗
PubMed1988

Event-related potentials and the matching of familiar and unfamiliar faces.

Event-related potentials (ERPs) were recorded from one midline and three pairs of lateral sites while subjects made same/different judgements on sequentially presented pairs of familiar or unfamiliar faces. During the interval between the first and second face, a slow wave was more negative-going over the right than the left hemisphere, particularly when the faces were familiar. Following the second face, two regions of the waveforms were more negative-going when this face did not match the identity of its predecessor. In the early region (less than 160 msec), this effect was confined to posterior electrode sites and familiar faces. In the later region (greater than 250 msec), the match/non-match effect was widespread across the scalp and was evident for both familiar and non-familiar faces, although in the latency range 350-450 msec (encompassing the "N400" component), it was greater in magnitude in the case of familiar stimuli. It is suggested that the slow wave asymmetries reflect the engagement of short-term memory mechanisms lateralized to the right hemisphere. The match/non-match differences are thought to reflect multiple processes, including the modulation of the "N400" component. The sensitivity of this component to the familiarity manipulation is consistent with the hypothesis that the amplitude of N400 reflects an item's compatibility with currently activated memory representations.

Adult↗
PubMed1990

Implicit learning of new faces in prosopagnosia: an application of the mere-exposure paradigm.

A prosopagnosic patient was shown faces with which he had no prior experience, and was then given two-alternative forced choice recognition ("which of these faces did you see before?") and preference ("which of these faces do you like better?") tasks to assess learning. The patient showed normal preference for target faces, despite the fact that recognition of the faces was nil. This suggests that at least some prosopagnosics show implicit learning of new faces. The patient's normal preference for target faces is conceptualized as a "perceptual fluency" effect similar to that seen in more global forms of amnesia.

Adult↗
PubMed1995

Face perception and within-category discrimination in prosopagnosia.

Prosopagnosics are impaired at face recognition, but unimpaired, or relatively less impaired, at common object recognition. It has been suggested that this dissociation results simply from the greater difficulty of face recognition compared to object recognition, or from the greater need to discriminate visually similar members of a single category in face recognition compared to object recognition. We tested these hypotheses using the performance of normal subjects in an 'old/new' recognition paradigm to establish the true relative difficulty of face and object recognition, and required both normal subjects and a prosopagnosic subject to discriminate both faces and visually similar exemplars of nonface object categories. In two different experiments, the prosopagnosic patient performed disproportionately poorly with faces. These results disconfirm the hypotheses described above, and imply that prosopagnosia is an impairment of a specialized form of visual recognition that is necessary for face recognition and is not necessary, or less necessary, for the recognition of common objects.

Adult↗
PubMed1987

The responses of neurons in the cortex in the superior temporal sulcus of the monkey to band-pass spatial frequency filtered faces.

There are neurons in the cortex in the anterior part of the superior temporal sulcus of the macaque monkey with visual responses which would be useful for face recognition (Rolls, 1984; Baylis et al., 1985). To analyze further the information which leads them to respond, their responses were measured to parametrically filtered stimuli. The responses of 48 such single neurons were measured to faces which were digitized and were bandpass spatial frequency filtered. The octave width bands were 2-4, 4-8, 8-16, 16-32, 32-64 and 64-128 cycles per image. It was found that the neurons could respond well to single octaves of the spatial frequencies normally present in faces, that the most effective bands were 4-8, 8-16 and 16-32 cycles per face (cpf), and that the bands 2-4 and 32-64 cpf were partly effective. In investigations of whether the responses of the neurons to an unfiltered face, and to low-pass and high-pass filtered images could be predicted by linear addition of their responses to each of the octave bands shown separately, it was found that the majority of the neurons were non-linear, and responded much less than predicted. It was also shown that this occurred even when the contrast was reduced to 0.25 of that normally present in a face, so that the result was not due just to a ceiling effect of the maximum firing rate. These results help to define parametrically the aspects of the information normally present in a face which are sufficient to produce responses of these neurons to them, and show that linear operations cannot account for information processing in this part of the visual system.

Action Potentials↗
PubMed1988

Electrodermal discrimination of familiar but not unfamiliar faces in prosopagnosia.

It has been previously shown that prosopagnosics can electrodermally "recognize" faces they cannot verbally identify and with which they feel no familiarity. This study extended previous results by showing that electrodermal discrimination of faces exists only on a famous face identification task, and not on a matching-to-sample task involving unfamiliar faces. This suggests that electrodermal recognition reflects the activation of stored identity-specific information built up on the basis of past contact with faces, and provides a psychophysiological distinction between familiar and unfamiliar face processing. Implications for cognitive models of face recognition, and for understanding the nature of prosopagnosia, are discussed.

Agnosia↗
PubMed1996

Brain events related to normal and moderately scrambled faces.

The neural basis of normal and scrambled face processing was investigated by recording evoked potentials from 21 electrodes at standard EEG sites, with respect to a nose reference. Temporal negativities were found that result from two overlapping phenomena: they arise from the polarity reversal on temporal electrodes of the vertex P2, a positive wave peaking about 170-200 ms after the onset of a face stimulus, and also from an overlapping 'processing negativity' of long duration associated with the processing difficulty of the scrambled face stimulus. The comparisons of scalp potential and current density mappings support the proposal that some neuronal networks are active both for faces and scrambled faces and are compatible with the involvement of the superior temporal sulcus, the inferotemporal cortex and the parahippocampal and fusiform gyri, whereas the processing negativity would only involve the deepest generators of this network. Furthermore, the encoding of both faces and scrambled faces seems to take place predominantly in the right hemisphere.

Adult↗
PubMed2006

Effect of face familiarity on age decision.

The present experiment was planned to check whether the extraction of apparent age is affected by face identity (familiarity) or not. According to the traditional view, age estimation should be carried out independently of face identity, because it is one of the visually derived semantic codes (like gender and ethnicity). However, little is known about its underlying mechanisms. Moreover, some recent studies have cast doubt on the parallel thesis regarding facial expression, facial speech, ethnicity, and gender. Given the promising results of a pilot experiment (n=24), 16 Caucasian participants were enrolled in an "age decision" task on morphed faces derived from one old and one young source-face, in the proportion 70:30. The respondents had previously been familiarised with half the source faces by a learning procedure (associating the face, surname, occupation and city of residence of the person displayed), while the remaining half were unfamiliar. The results showed that age decision was affected by face familiarity, at least when the task was perceptually difficult enough. This adds support to the thesis that the identification of identity and the extraction of visually derived semantic codes are not made independently from each other. The status of age, within the visually derived semantic codes, is also discussed.

Aging↗
PubMed2005

Perceptual asymmetries are preserved in memory for highly familiar faces of self and friend.

We investigated the effect of familiarity on people's perception of facial likeness by asking participants to choose which of two mirror-symmetric chimeric images (made from the left or right half of a photograph of a face) looked more like an original image. In separate trials the participants made this judgment for their own face and for the face of a close friend; half of them matched to a true image of the original and half matched to a mirror image of the original. In the case of matching to a friend's face presented in the familiar orientation, over 80% of participants chose the left-left composite to be a better likeness to the original, whereas only 62% showed the same left-side bias when matching to a mirror image. The difference is significant, and the result contrasts markedly with a second experiment where participants who were unfamiliar with the faces showed comparable left-side biases when matching to true or mirror reversed images. The result suggests that perceptual asymmetries are retained in our long-term memory for highly familiar faces. While matching to images of self also showed an effect of familiarity, the data in this condition show less evidence of perceptual asymmetry and are discussed in relation to recent research on the representation of one's own face.

Adult↗
PubMed2004

Transfer between views of conspecific faces at different ages or in different orientations by sheep.

Sheep are able to discriminate photographs of conspecific faces. The present study investigates adult ewe's recognition of faces of the same animal between different ages or between different orientations. Twelve adult sheep were first trained to discriminate between faces of two unfamiliar animals, one of which was associated with a food reward. Transfer of discrimination from this pair to the same pair but at a different age, or in a different orientation, was then evaluated (transfer test), and compared with a new pair of the same condition (control test). Learned discrimination of a frontal view of unfamiliar 3-month-old lambs' faces improved subsequent discrimination of the same pair when they were 1-month-old in comparison to discrimination of new 1-month-old faces. Moreover, sheep that were trained to discriminate frontal views of unfamiliar adult individuals discriminated profile views of the same animals more accurately than that of novels. However, learned discrimination of the profile view of unfamiliar adult faces had no effect on subsequent discrimination of the frontal view of that same pair. These results suggest that to some extent sheep recognise faces of unfamiliar animals at different ages and in different orientations.

Animals↗
PubMed2006

Face processing limitation to own species in primates: a comparative study in brown capuchins, Tonkean macaques and humans.

Most primates live in social groups which survival and stability depend on individuals' abilities to create strong social relationships with other group members. The existence of those groups requires to identify individuals and to assign to each of them a social status. Individual recognition can be achieved through vocalizations but also through faces. In humans, an efficient system for the processing of own species faces exists. This specialization is achieved through experience with faces of conspecifics during development and leads to the loss of ability to process faces from other primate species. We hypothesize that a similar mechanism exists in social primates. We investigated face processing in one Old World species (genus Macaca) and in one New World species (genus Cebus). Our results show the same advantage for own species face recognition for all tested subjects. This work suggests in all species tested the existence of a common trait inherited from the primate ancestor: an efficient system to identify individual faces of own species only.

Adult↗
PubMed2006

Time-varying amygdala response to emotional faces in generalized social phobia.

BACKGROUND: Individuals with social phobia (SP) have altered behavioral and neural responses to emotional faces and are hypothesized to have deficits in inhibiting emotion-related amygdala responses. We tested for such amygdala deficits to emotional faces in a sample of individuals with SP. METHOD: We used functional magnetic resonance imaging (fMRI) to examine the neural substrates of emotional face processing in 14 generalized SP (gSP) and 14 healthy comparison (HC) participants. Analyses focused on the temporal dynamics of the amygdala, prefrontal cortex (PFC), and fusiform face area (FFA) across blocks of neutral, fear, contempt, anger, and happy faces in gSP versus HC participants. RESULTS: Amygdala responses in participants with gSP occurred later than the HC participants to fear, angry, and happy faces. Parallel PFC responses were found for happy and fear faces. There were no group differences in temporal response patterns in the FFA. CONCLUSIONS: This finding might reflect a neural correlate of atypical orienting responses among individuals with gSP. Commonly reported SP deficits in habituation might reflect neural regions associated with emotional self-evaluations rather than the amygdala. This study highlights the importance of considering time-varying modulation when examining emotion-related processing in individuals with gSP.

Adult↗
PubMed2006

Inversion and contrast-reversal effects on face processing assessed by MEG.

The processing of upright, inverted and contrast-reversed faces was investigated using MEG. Peak and global field power analyses revealed that the M100, M170 and M220 components were delayed for inverted and contrast-reversed compared to normal upright faces but no amplitude modulations were found. Source analyses using an event-related SAM beamformer technique revealed bilateral occipital sources for the M100 and M220 components. For the M170, two distinct sources simultaneously active were found, a bilateral and posterior source (M170A) and a right lateralized ventral and more anterior source (M170B) around the fusiform gyrus. None of the sources varied in location or intensity between face types. However, although different from the M100, the location of the M170A was not significantly different from that of the M220, suggesting the latter could be a reactivation of the former. Confirming previous ERP results on the processing of inverted faces, the present study extends the findings to contrast-reversed face stimuli and suggests that deviations from the standard upright face format do not activate extra areas but simply result in the delayed activation of the sources generating the M100, M170 and M220 components. The data confirm the sensitivity of the M100 to face manipulations and further suggest that the M170 is generated by two distinct sources, one of which situated in occipital extrastriate areas (M170A) could be reactivated around 220 ms to generate the M220 component.

Adult↗
PubMed2003

Successful episodic memory retrieval of newly learned faces activates a left fronto-parietal network.

It is easier to recognize a familiar face than a newly learned face. The neural basis of familiar face recognition has been elucidated in functional imaging and lesion studies. Behavioural and neuropsychological data indicate, however, that brain systems involved in episodic retrieval of familiar and newly learned faces are distinct. In our study, 12 subjects viewed 30 novel faces in an encoding session. In the study condition, event-related functional magnetic resonance imaging (fMRI) was used to compare brain activation during correct recognition of the recently learned faces to that observed during correct rejection of unknown control faces. Differences were present in the left inferior parietal (BA 40) and left medial frontal/anterior cingulate (BA 32/9) cortex. These two regions may be part of a pathway in the dorsal visual stream, responsible for a "feeling of familiarity" in contrast to the ventral pathway in the temporal lobes, which is mainly involved in the recognition of personal identity.

Adult↗