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Biomedical subjects

D I Perrett

Publications and source records attributed to D I Perrett.

At least 19 recordsLinked to original sources
PubMed2002

Partnership status and the temporal context of relationships influence human female preferences for sexual dimorphism in male face shape.

Secondary sexual characteristics may indicate quality of the immune system and therefore a preference for masculinity may confer genetic benefits to offspring; however, high masculinity may be associated with costs of decreased paternal investment. The current study examined women's preferences for masculinity in male faces by using computer graphics to allow transformation between feminine and masculine versions of individual male faces. We found that preferences for masculinity are increased when women either have a partner or are considering a short-term relationship. Such preferences are potentially adaptive, serving to: (i) maximize parental investment and cooperation in long-term relationships by biasing choices towards feminine faced males, and (ii) maximize possible good-gene benefits of short-term or extra-pair partners by biasing choices towards masculine faced males. We also found that individuals using oral contraception do not show the above effects, indicating that such hormonal intervention potentially disrupts women's choices for evolutionarily relevant benefits from males.

Adolescent↗
PubMed2001

Symmetry, sexual dimorphism in facial proportions and male facial attractiveness.

Facial symmetry has been proposed as a marker of developmental stability that may be important in human mate choice. Several studies have demonstrated positive relationships between facial symmetry and attractiveness. It was recently proposed that symmetry is not a primary cue to facial attractiveness, as symmetrical faces remain attractive even when presented as half faces (with no cues to symmetry). Facial sexual dimorphisms ('masculinity') have been suggested as a possible cue that may covary with symmetry in men following data on trait size/symmetry relationships in other species. Here, we use real and computer graphic male faces in order to demonstrate that (i) symmetric faces are more attractive, but not reliably more masculine than less symmetric faces and (ii) that symmetric faces possess characteristics that are attractive independent of symmetry, but that these characteristics remain at present undefined.

Face↗
PubMed2001

Self-perceived attractiveness influences human female preferences for sexual dimorphism and symmetry in male faces.

Exaggerated sexual dimorphism and symmetry in human faces have both been linked to potential 'good-gene' benefits and have also been found to influence the attractiveness of male faces. The current study explores how female self-rated attractiveness influences male face preference in females using faces manipulated with computer graphics. The study demonstrates that there is a relatively increased preference for masculinity and an increased preference for symmetry for women who regard themselves as attractive. This finding may reflect a condition-dependent mating strategy analogous to behaviours found in other species. The absence of a preference for proposed markers of good genes may be adaptive in women of low mate value to avoid the costs of decreased parental investment from the owners of such characteristics.

Adolescent↗
PubMed2001

The speed of sight.

Macaque monkeys were presented with continuous rapid serial visual presentation (RSVP) sequences of unrelated naturalistic images at rates of 14--222 msec/image, while neurons that responded selectively to complex patterns (e.g., faces) were recorded in temporal cortex. Stimulus selectivity was preserved for 65% of these neurons even at surprisingly fast presentation rates (14 msec/image or 72 images/sec). Five human subjects were asked to detect or remember images under equivalent conditions. Their performance in both tasks was above chance at all rates (14--111 msec/image). The performance of single neurons was comparable to that of humans and responded in a similar way to changes in presentation rate. The implications for the role of temporal cortex cells in perception are discussed.

Animals↗
PubMed2001

Administration of the beta-adrenoceptor blocker propranolol impairs the processing of facial expressions of sadness.

RATIONALE: Noradrenergic processes within the amygdala have been implicated in the modulation of memory for emotional material. The amygdala has also been associated with the processing of facial expressions of emotion, particularly those of fear and sadness. However, the role of noradrenaline in the latter process is unknown. OBJECTIVE: Therefore the present study examined the effect of an oral beta-blocker (propranolol, 80 mg) upon facial expression recognition in healthy volunteers. METHODS: Facial expressions of six basic emotions, which had been "morphed" between neutral and each emotional standard, were used in the recognition task. Subjects completed this task both before and 1 h following either propranolol or a placebo. Control measures of choice reaction time and vigilance performance were also included to assess any non-specific effects of the drug upon alertness and speed. RESULTS: The administration of propranolol, relative to placebo, specifically increased reaction time to identify facial expressions of sadness correctly, in the absence of changes in speed to recognise other facial expressions of emotion. Subjective ratings of mood and alertness as well as speed in the two control tasks were not altered by propranolol, arguing against an account in terms of general sedation. CONCLUSIONS: These data suggest that noradrenergic processes are not only involved in memory for emotional material but also in the evaluation of sadness from facial expression. The selective nature of this effect adds to evidence suggesting that the recognition of different expressions of emotion depends upon at least partly separable neural processes. A role for noradrenaline in recognising sadness in others has potential relevance for our understanding of disorders characterised by disturbances in emotional processing.

Administration, Oral↗
PubMed2001

Neuronal representation of disappearing and hidden objects in temporal cortex of the macaque.

Neurons in the anterior regions of the banks of the superior temporal sulcus (STSa) of the macaque monkey respond to the sight of biologically significant stimuli such as faces, bodies and their motion. In this study the responses of STSa neurons were recorded during the gradual occlusion of the experimenter and other mobile objects behind screens at distances of 0.5-4 m from the monkeys. The experimenter or other object remained out of sight for 3-15 s before emerging back in to view. We describe a population of neurons (n=33) showing increased activity during the occlusion of objects that was maintained for up to 11 s following complete occlusion (when only the occluder itself was visible). This increase in activity was selective for the position of the occlusion within the testing room. Many neurons showed little or no change in activity prior to occlusion when the object or experimenter was completely in view. By coding for the presence and location of recently occluded objects, these responses may contribute to the perceptual capacity for object permanence.

Action Potentials↗
PubMed2001

Imitation, mirror neurons and autism.

Various deficits in the cognitive functioning of people with autism have been documented in recent years but these provide only partial explanations for the condition. We focus instead on an imitative disturbance involving difficulties both in copying actions and in inhibiting more stereotyped mimicking, such as echolalia. A candidate for the neural basis of this disturbance may be found in a recently discovered class of neurons in frontal cortex, 'mirror neurons' (MNs). These neurons show activity in relation both to specific actions performed by self and matching actions performed by others, providing a potential bridge between minds. MN systems exist in primates without imitative and 'theory of mind' abilities and we suggest that in order for them to have become utilized to perform social cognitive functions, sophisticated cortical neuronal systems have evolved in which MNs function as key elements. Early developmental failures of MN systems are likely to result in a consequent cascade of developmental impairments characterised by the clinical syndrome of autism.

Autistic Disorder↗
PubMed2000

Caricaturing facial expressions.

The physical differences between facial expressions (e.g. fear) and a reference norm (e.g. a neutral expression) were altered to produce photographic-quality caricatures. In Experiment 1, participants rated caricatures of fear, happiness and sadness for their intensity of these three emotions; a second group of participants rated how 'face-like' the caricatures appeared. With increasing levels of exaggeration the caricatures were rated as more emotionally intense, but less 'face-like'. Experiment 2 demonstrated a similar relationship between emotional intensity and level of caricature for six different facial expressions. Experiments 3 and 4 compared intensity ratings of facial expression caricatures prepared relative to a selection of reference norms - a neutral expression, an average expression, or a different facial expression (e.g. anger caricatured relative to fear). Each norm produced a linear relationship between caricature and rated intensity of emotion; this finding is inconsistent with two-dimensional models of the perceptual representation of facial expression. An exemplar-based multidimensional model is proposed as an alternative account.

Adult↗
PubMed2000

Neural representation for the perception of the intentionality of actions.

A novel population of cells is described, located in the anterior part of the superior temporal sulcus (STSa, sometimes called STPa) of the temporal lobe in the macaque monkey. These cells respond selectively to the sight of reaching but only when the agent performing the action is seen to be attending to the target position of the reaching. We describe how such conditional selectivity can be generated from the properties of distinct cell populations within STSa. One cell population responds selectively to faces, eye gaze, and body posture, and we argue that subsets of these cells code for the direction of attention of others. A second cell population is selectively responsive to limb movement in certain directions (e.g., responding to an arm movement to the left but not to an equivalent leg movement or vice versa). The responses of a subset of cells sensitive to limb movement are modulated by the direction of attention (indicated by head and body posture of the agent performing the action). We conclude that this combined analysis of direction of attention and body movements supports the detection of intentional actions.

Animals↗
PubMed2000

Manipulation of colour and shape information and its consequence upon recognition and best-likeness judgments.

Previous forays into the study of recognition have revealed an advantage for line-drawn and photographic shape caricatures of faces in reaction-time paradigms. When a presentation-time technique was used, photographs with enhanced colour intensity and saturation were also found to provide superior recognition accuracy to veridical images. This has provided strong evidence that distinctive information can produce a recognition advantage for famous faces in both colour and shape domains. Such a presentation-time paradigm allows the display of stimuli over a range of brief display periods. Using this paradigm, subjects recognised photorealistic target faces caricatured in shape with greater accuracy than veridical images, consistent with previous findings when reaction time was used as a measure. Subjects were also asked to identify the best likeness for individuals using photorealistic stimuli and an interactive paradigm with shape caricature, colour caricature, and contrast control varied by the user in real-time. The best likeness with shape manipulation was a slight anticaricature, while with colour-caricature and contrast-control images a mildly exaggerated image was selected as the best likeness. Thus, although images caricatured substantially in colour or shape (+40%) induce superior recognition compared to veridical images, such substantial exaggerations are not necessarily seen as best likenesses under prolonged exposure.

Color↗
PubMed1999

Dissociable neural responses to facial expressions of sadness and anger.

Previous neuroimaging and neuropsychological studies have investigated the neural substrates which mediate responses to fearful, disgusted and happy expressions. No previous studies have investigated the neural substrates which mediate responses to sad and angry expressions. Using functional neuroimaging, we tested two hypotheses. First, we tested whether the amygdala has a neural response to sad and/or angry facial expressions. Secondly, we tested whether the orbitofrontal cortex has a specific neural response to angry facial expressions. Volunteer subjects were scanned, using PET, while they performed a sex discrimination task involving static grey-scale images of faces expressing varying degrees of sadness and anger. We found that increasing intensity of sad facial expression was associated with enhanced activity in the left amygdala and right temporal pole. In addition, we found that increasing intensity of angry facial expression was associated with enhanced activity in the orbitofrontal and anterior cingulate cortex. We found no support for the suggestion that angry expressions generate a signal in the amygdala. The results provide evidence for dissociable, but interlocking, systems for the processing of distinct categories of negative facial expression.

Adult↗
PubMed1998

Effects of sexual dimorphism on facial attractiveness.

Testosterone-dependent secondary sexual characteristics in males may signal immunological competence and are sexually selected for in several species. In humans, oestrogen-dependent characteristics of the female body correlate with health and reproductive fitness and are found attractive. Enhancing the sexual dimorphism of human faces should raise attractiveness by enhancing sex-hormone-related cues to youth and fertility in females, and to dominance and immunocompetence in males. Here we report the results of asking subjects to choose the most attractive faces from continua that enhanced or diminished differences between the average shape of female and male faces. As predicted, subjects preferred feminized to average shapes of a female face. This preference applied across UK and Japanese populations but was stronger for within-population judgements, which indicates that attractiveness cues are learned. Subjects preferred feminized to average or masculinized shapes of a male face. Enhancing masculine facial characteristics increased both perceived dominance and negative attributions (for example, coldness or dishonesty) relevant to relationships and paternal investment. These results indicate a selection pressure that limits sexual dimorphism and encourages neoteny in humans.

Adult↗
PubMed1998

Evidence accumulation in cell populations responsive to faces: an account of generalisation of recognition without mental transformations.

In this paper we analyse the time course of neuronal activity in temporal cortex to the sight of the head and body. Previous studies have already demonstrated the impact of view, orientation and part occlusion on individual cells. We consider the cells as a population providing evidence in the form of neuronal activity for perceptual decisions related to recognition. The time course on neural responses to stimuli provides an explanation of the variation in speed of recognition across different viewing circumstances that is seen in behavioural experiments. A simple unifying explanation of the behavioural effects is that the speed of recognition of an object depends on the rate of accumulation of activity from neurones selective for the object, evoked by a particular viewing circumstance. This in turn depends on the extent that the object has been seen previously under the particular circumstance. For any familiar object, more cells will be tuned to the configuration of the object's features present in the view or views most frequently experienced. Therefore, activity amongst the population of cells selective for the object's appearance will accumulate more slowly when the object is seen in an unusual view, orientation or size. This accounts for the increased time to recognise rotated views without the need to postulate 'mental rotation' or 'transformations' of novel views to align with neural representations of familiar views.

Attention↗
PubMed1998

The 'Ideal Homunculus': decoding neural population signals.

Information processing in the nervous system involves the activity of large populations of neurons. It is possible, however, to interpret the activity of relatively small numbers of cells in terms of meaningful aspects of the environment. 'Bayesian inference' provides a systematic and effective method of combining information from multiple cells to accomplish this. It is not a model of a neural mechanism (neither are alternative methods, such as the population vector approach) but a tool for analysing neural signals. It does not require difficult assumptions about the nature of the dimensions underlying cell selectivity, about the distribution and tuning of cell responses or about the way in which information is transmitted and processed. It can be applied to any parameter of neural activity (for example, firing rate or temporal pattern). In this review, we demonstrate the power of Bayesian analysis using examples of visual responses of neurons in primary visual and temporal cortices. We show that interaction between correlation in mean responses to different stimuli (signal) and correlation in response variability within stimuli (noise) can lead to marked improvement of stimulus discrimination using population responses.

Animals↗
PubMed1997

A specific neural substrate for perceiving facial expressions of disgust.

Recognition of facial expressions is critical to our appreciation of the social and physical environment, with separate emotions having distinct facial expressions. Perception of fearful facial expressions has been extensively studied, appearing to depend upon the amygdala. Disgust-literally 'bad taste'-is another important emotion, with a distinct evolutionary history, and is conveyed by a characteristic facial expression. We have used functional magnetic resonance imaging (fMRI) to examine the neural substrate for perceiving disgust expressions. Normal volunteers were presented with faces showing mild or strong disgust or fear. Cerebral activation in response to these stimuli was contrasted with that for neutral faces. Results for fear generally confirmed previous positron emission tomography findings of amygdala involvement. Both strong and mild expressions of disgust activated anterior insular cortex but not the amygdala; strong disgust also activated structures linked to a limbic cortico-striatal-thalamic circuit. The anterior insula is known to be involved in responses to offensive tastes. The neural response to facial expressions of disgust in others is thus closely related to appraisal of distasteful stimuli.

Adult↗
PubMed1997

Computer-enhanced emotion in facial expressions.

Benson & Perrett's (1991 b) computer-based caricature procedure was used to alter the positions of anatomical landmarks in photographs of emotional facial expressions with respect to their locations in a reference norm face (e.g. a neutral expression). Exaggerating the differences between an expression and its norm produces caricatured images, whereas reducing the differences produces 'anti-caricatures'. Experiment 1 showed that caricatured (+50% different from neutral) expressions were recognized significantly faster than the veridical (0%, undistorted) expressions. This held for all six basic emotions from the Ekman & Friesen (1976) series, and the effect generalized across different posers. For experiment 2, caricatured (+50%) and anti-caricatured (-50%) images were prepared using two types of reference norm; a neutral-expression norm, which would be optimal if facial expression recognition involves monitoring changes in the positioning of underlying facial muscles, and a perceptually-based norm involving an average of the expressions of six basic emotions (excluding neutral) in the Ekman & Friesen (1976) series. The results showed that the caricatured images were identified significantly faster, and the anti-caricatured images significantly slower, than the veridical expressions. Furthermore, the neutral-expression and average-expression norm caricatures produced the same pattern of results.

Adult↗
PubMed1997

Facial expression megamix: tests of dimensional and category accounts of emotion recognition.

We report four experiments investigating the perception of photographic quality continua of interpolated ('morphed') facial expressions derived from prototypes of the 6 emotions in the Ekman and Friesen (1976) series (happiness, surprise, fear, sadness, disgust and anger). In Experiment 1, morphed images made from all possible pairwise combinations of expressions were presented in random order; subjects identified these as belonging to distinct expression categories corresponding to the prototypes at each end of the relevant continuum. This result was replicated in Experiment 2, which also included morphs made from a prototype with a neutral expression, and allowed 'neutral' as a response category. These findings are inconsistent with the view that facial expressions are recognised by locating them along two underlying dimensions, since such a view predicts that at least some transitions between categories should involve neutral regions or identification as a different emotion. Instead, they suggest that facial expressions of basic emotions are recognised by their fit to discrete categories. Experiment 3 used continua involving 6 emotions to demonstrate best discrimination of pairs of stimuli falling across category boundaries; this provides further evidence of categorical perception of facial expressions of emotion. However, in both Experiment 1 and Experiment 2, reaction time data showed that increasing distance from the prototype had a definite cost on ability to identify emotion in the resulting morphed face. Moreover, Experiment 4 showed that subjects had some insight into which emotions were blended to create specific morphed images. Hence, categorical perception effects were found even though subjects were sensitive to physical properties of these morphed facial expressions. We suggest that rapid classification of prototypes and better across boundary discriminability reflect the underlying organisation of human categorisation abilities.

Adult↗