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Part III
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Psychological Aspects of Disease
Aspects ofFacial Esthetics
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andDisgurement
ChristophRunte andDieterDirksen
14
14.1 Introduction
Why do human faces look the way they do? And how do we judge attractiveness? Still we do not have nal answers to these and related questions [1, 2], but recently, science has at least found some clues.
Through the centuries, there have been many attempts to nd out how beauty in general and beauty of the human face in particular are deter­mined. Beauty has been equated with truth [3], usefulness [4], and good [5]. The French novel­ist Marie-Henri Beyle, better known as Stendhal, noted beauty was nothing other than the “prom­ise of happiness” [6], which means that we are attracted to objects or persons which might help us to get happy, and this attraction is what we call beauty, but this only shifts the problem to the denition of happiness. If happiness is to live in the company of trustworthy [7], healthy [8], and guiding [9] people, faces are believed to reveal those qualities [10]. Evolutionary biology would explain beauty, or, strictly speaking, attractiveness, mainly with regard to mate selec­tion as a product of selection by survival and sexual selection. Another evolutionary aspect of beauty and disgurement is its inuence on parental care [11, 12]. There have been attempts
C. Runte (*) · D. Dirksen Department of Prosthodontics, University of Münster, Münster, Germany e-mail: crunte@uni-muenster.de
to describe beauty as a consequence of the adher­ence to objective morphologic parameters, e.g., bilateral symmetry and certain proportions. Other authors countered that the beauty of a per­son or an object might be judged differently by different persons, which leads to the conclusion that beauty is “not judged objectively but accord­ing to the beholders estimation” (Theocritus [13]). In his Critique of Judgment, Immanuel Kant [14] dened beauty as something causing pleasure without any interest and understanding. Kant then continued that if beauty was caused by the pleasing perception without personal inter­est, it should be pleasing to every beholder. Therefore, beauty as a universally pleasing per­ception would be mistaken as a logically deduc­ible quality of the object. However, later philosophers dismissed Kant’s idea of pleasure without interest.
After all these attempts, still there seems to be no simple explanation or geometrical formula to dene beauty in detail, and, as many people agree in their esthetic judgment on who is attractive and who is not, beauty seems not only to depend on a beholders’ free and unconditioned estimation.
An individual, intuitive judgment of beauty in general seems to be determined by the process of visual perception, sociocultural conditions, and individual experience. Chelsea Wald [2] recently summed up four fundamental open questions on beauty, starting with the problem of its denition: “What is the point of human beauty?”
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Beauty and disgurement are often used as opposites, as we did in the chapter title. However, disgurement and beauty are not mutually exclu­sive. If beauty is at least partially judged by the beholder, its opposite would also be subject to the beholder’s estimation. Disgurement is as dif­cult to dene as it is true for beauty. If we use disgurement as the opposite of the given deni­tions of beauty, disgurement could be dened as equal to falsity, futility, and bad. It could be described as the “promise of bad luck” or the vio­lation of proportional rules. As an opposite of Kant’s denition, disgurement would be a per­ception that is unpleasant without interest and understanding. None of these denitions is truly convincing.
14.2 Biological Aspects ofFacial
Beauty andDisgurement
As it has been said before, beauty may be seen as an aspect of perception (“in the eye of the beholder”) or as a result of certain morphologic properties. We will therefore discuss these aspects of perception and of morphogenesis in more detail.
14.2.1 Visual Perception andits
Inuence ontheEsthetic Judgment
All humans share fundamental physiologic pro­cesses of visual perception and recognition. Visual perception and recognition enable us to experience the world around us, beginning with the faces of our parents. It is necessary to under­stand these processes because they are the reason why our visual perception is selective and also why our judgment of the beauty of a face is not free and according to our individual assessment.
The rst step of visual perception is light entering the eye bulb through the lens and being projected to the retina. Here, the photon energy is transformed into chemical energy. Illuminated rhodopsins activate G-proteins, which then start the signal transduction. At this stage the signal
represents an excitation at a specic point of the two-dimensional retina with information on loca­tion, brightness (rods and cones), and color (cones). Passing through the layer of retina bipo­lar cells, the signals of a number of photorecep­tors from a receptive eld are collected by a third neuron (retinal ganglion cell). There are different types of retinal ganglion cells; on-cells will trans­mit a signal with a higher ring rate if the input signal from center of the receptive eld is more intense than in the peripheral areas. Off-cells would show a reverse reaction. The ganglion cell axons follow the optical nerve with the informa­tion from the median part of the retina crossing to the contralateral hemisphere (chiasma opticum) while the information from the lateral part remains on the same side.
The next signal transformation step (located in the corpus geniculatum laterale) is an extraction of edges or outlines with a high contrast. The visual information is then projected primarily to the occipital visual cortex. The signal transfor­mation to outlines is illustrated in Fig. 14.1. Understanding of this fundamental process of visual perception was founded in the late 1950s by David Hubel and Torsten Wiesel with their experiments on the cat’s striate cortex [15]. Larsson et al. [16] conrmed the account of structures with high contrast to pattern recogni­tion. However, the ability to recognize faces with only a few outlines from a sketch or even from randomly distributed elements has been well known for centuries. In his treatise on painting, Leonardo da Vinci [17] claimed that “by looking attentively at old and smeared walls or stones and veined marble of various colors, you may fancy that you see in them several compositions, [… and] strange countenances […]. By these con­fused lines the inventive genius is excited to new exertions.”
Efferences from the corpus geniculatum later­ale also reach the superior collicles, which are important for eye movements. They send signals to nuclei of the cranial nerves (esp. oculomotor, trochlear, and abducens nerve) and the pulvinar (central medial, posterior inferior, and middle inferior pulvinar nuclei [18]). If a visual stimulus is presented, the following eye movements are
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Fig. 14.1 Steps of visual perception simulated by digital
image processing– original picture (left), the signal high­pass ltered and posterized (middle) and reduced to areas below a brightness threshold (right). By these simple pro­cedures, the image is reduced to lines indicating the con­tours, but recognition of the object is still possible. Data is correspondingly reduced from 389KB (.tif-format, LZW­compressed le from left image) to 90KB (same format, right). With similar procedures, visual recognition is
directed in a way to “track” the areas of high brightness contrast. This “tracking” was exam­ined and described by Alfred Yarbus [19], who also identied a special area of interest within the face, called the “Yarbus triangle.” This triangle is dened by the eyes and mouth (Fig. 14.2). Consequently, Karl Popper and John Eccles [20] compared the process of visual perception to the painting of a picture, not to the taking of a photo­graph. Subsequent studies showed that there is also a dominance of the left “eld of gaze” [
21] if
we are looking at a face. There was no preference of one side of the eld of gaze when looking at other, nearly symmetrical gures. Thus, the right side of the face might have more impact on the esthetic judgment than the left one. Interestingly, Meyer-Marcotty et al. [22] found that subjects affected by cleft lip and palate focus their atten­tion on the upper lip and nose if they look at the faces of healthy persons.
Visual stimuli showing regular geometry [23], reection symmetry [24], familiar shapes, or matching expectations [25, 26] are supposed to
focused on contour lines. These lines are not restricted to physical boundaries of the object. Lines of contrast can also be caused by color or material changes and by light­ing and reection at curvatures and edges, e.g., at the eye­lids, nose, ears, and philtrum. The pictures of Nefertiti were generated using the 3D model “bust of Nefertiti at the Neues Museum, Berlin” (
com/object/3d- print- bust- of- nefertiti- at- the- egyptian­museum- berlin- 2951)
Fig. 14.2 The Yarbus triangle is a region of the face
where structures with high contrast are more frequently focused than other regions. In his original publication from 1967, Yarbus [19] used pictures from faces and also one from a bust of Nefertiti (in prole) and simultane­ously recorded the eye movements. With his technique, he could superimpose eye movement tracing with the visual stimuli
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draw the viewer’s attention to themselves, espe­cially if they show clearly visible outlines within the Yarbus triangle.
In recent studies it was shown that perception of faces is different from perception of other famil­iar objects in view. A fast and intense neuronal response to visual stimuli called the N170 effect is selective for faces in certain areas of the brain [27]. The source of this neuronal response to the presen­tation of faces is located primarily in the right fusi­form and infratemporal gyri, especially in regions called inferior occipital gyrus face area (OFA) and fusiform face area (FFA, [28]). Damage or intra­cranial stimulation of the FFA is associated with the disability to recognize faces (prosopagnosia, [29]). However, these areas are only part of a dis- tributed neural network responsible for face recog­nition [30]. Prosopagnosia can also be caused by injuries of the temporal lobe, e.g., after surgical treatment of epilepsia. Recent studies indicate that the ventral anterior temporal lobe plays an impor­tant role in person-specic face perception [31]. However, the question how the different parts of our brain inuence our esthetic judgment in detail remains largely unanswered.
Our knowledge on visual perception suggests that the fundament for our esthetic judgment is focused on facial structures, especially those within the Yarbus triangle, showing clear outlines of high contrast. As a consequence, these struc­tures will be of importance in the denition of beautiful properties, e.g., using facial proportions.
However, the determination of an objects’ physical shape is only the start of a process of recognition and assessment. Eleanor Rosch [32,
33] tested older concepts of Gestalt psychology
experimentally and found that there are “ideal types” of perceptual stimuli, e.g., colors. These prototypes represent the “clearest cases, best examples” of a category (“a concept designatable by words”). A perceptual stimulus is therefore evaluated by comparison to the prototype of its category [1]. Whether a visual stimulus will cause pleasure or disgust will therefore largely depend on its categorization. For example, one person might react with disgust to the view of an oyster, another one with pleasure. The difference cannot be explained by the shape or texture of the oyster itself, but by the presentation and the per-
sonal experience one (or her/his social environ­ment) has with oysters and if it is reasonable to categorize the oyster as delicacy. Tattoos and piercings have been held in very different degrees of regard in different times and cultures. Examples from the orofacial region are “decora­tive crowns” and “dental grills” among certain ethnic groups and cultural scenes [34]. The pol­ished metallic surfaces of crowns or amalgam llings found their own esthetic reverence in den­tal professionals in the past. However, this assess­ment was not always shared by patients. The more natural look of composite resins and ceramic veneers changed the view on metallic restorations. Within one category, perceptual stimuli are compared to the prototype. It has been assumed that the closer the stimulus ts to the prototype, the more pleasing it will be. On the other hand, typical stimuli are assumed to be more difcult to remember [35].
Classifying human beings into categories, especially by a look at their face, is problematic. Racism, nationalism, and class consciousness are only a few and extreme examples for the classi­cation connected to discrimination. At least, con­scious or unconscious classication will have a great inuence on our esthetic judgment. Prototype theory assumes that objects or subjects will cause pleasure if they are “prototypical” for their category [1].
When a visual stimulus has been matched to the category “face.” studies of Oosterhoff and Todorov [36] suggested that it will be evaluated basically on the two dimensions, “valence” and “dominance.” Thus, the beholder gathers infor­mation from facial cues whether the person approaching is harmless or harmful and physi­cally capable of implementing his intentions. These cues can be found mostly in the eye and mouth region, e.g., if the eyebrows are lifted, the resulting signal is trustworthiness.
14.2.2 Evolutionary Biology, Beauty,
andAverageness
Facial morphogenesis, the inuence of facial properties on mate selection and parental care, and the inheritance of genes regulating them are
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connected by the complex mechanisms of evolu­tionary biology. A current publication by Xiong etal. [37] listed a number of gene loci associated with different facial proportions within the Yarbus triangle. Although there still are many open ques­tions on human facial morphogenesis and how it has evolved, a simple example may illustrate some of the possible ways of facial development over generations. Stalk-eyed ies exhibit bizarre head morphology [38]. Arthropod body plan is very different to the human one, but evolutionary mechanisms are the same. Although it has been assumed that a wider interocular distance would be benecial in stereoscopic viewing (Fig.14.3), this argument is not convincing, as there are also drawbacks like the necessity to calculate an increased parallaxis for spatial perception and possible handicaps in ight. However, there is evidence for a connection between a large eye­span and “good genes” as only ies in good con­dition develop wide eyespans. If a wider eyespan is a signal for “good genes,” the idea of female ies preferring male ones with a wider interocu-
lar distance would be convincing (Fig.14.4). A third mechanism is caused by an X-chromosomal meiotic drive that can be suppressed by genetic factors associated with male y wide eyespan (Fig.14.5).
Evolutional biology would suggest that an advantageous feature would automatically become the average by elimination of other variants.
However, a connection between beauty and averageness has been postulated even before Darwin’s publications. In his Critique of Judgment, Kant [14] described how he thought our perception of beauty was inuenced by the average image of our visual experiences: He described how our imagination recalls form and view of a subject and is capable of “adding” all views of a certain kind, e.g., of a man. And to his belief, somebody who has seen a thousand men can estimate the average stature by super­imposing a lot of or even all of the thousand images in his mind. The outlines of the average man would then also represent the stature of a beautiful man.
Natural selection by survival: Narrow interocular distance is associated with lower cahnce of survival
Next Generation with higher proportion of genes from male files with longer interocular distance
Fig. 14.3 Stalk-eyed ies exhibit unusual facial proper-
ties with exaggerated eyespan (schematic representation). This was assumed to be a result of functional adaptation caused by an improved stereoscopic perception advanta-
geous for survival, but the more convincing explanation is that only ies in good condition (with “good genes”) exhibit a wide eyespan. Thus, a wide eyespan is not the reason for but the result of an advantage in survival
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Natural selection by survival: Interocular distance has no influence on survival (or larger eyespan is even disadvantageous)
Next Generation with higher proportion of genes from male files with longer interocular distance
Fig. 14.4 Another mechanism is sexual selection. In this example, female ies preferably choose male ies with wider
eyespan as mates
Female files prefer male ones
sexual selection:
with larger eyespan
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Superimposition of images became possible with the introduction of photography in the nine­teenth century. In 1883, Francis Galton [39] pub­lished his Inquiries into Human Faculty and Its Development. He observed that “All composites are better looking than their components, because the averaged portrait of many persons is free from the irregularities that variously blemish the looks of each of them.”
Evolutionary biology can explain a connec­tion between facial attractiveness and average­ness, following two basic concepts: On the one hand, average shapes could simply be the fea­tures of the most successful subjects (Fig.14.6). On the other hand, subjects with attractive facial features should have a higher reproductive suc­cess (Fig.14.7). However, being attracted to cer­tain facial shapes that are signs of success (sign for “good genes”) would be an advantageous strategy in mate choice, and these properties would prevail over the generations.
In addition to “survival of the ttest” and “reproduction of the most attractive,” there are even more evolutionary mechanisms to be taken
into consideration. If a small population gets iso­lated, e.g., on a distant island, and an above­average number of individuals bearing certain “founder mutation” passes through this evolu­tionary “bottleneck,” the following generations will show a high percentage of this mutation and also a reduced genetic variation (Fig.14.8), even though this mutation might be indifferent to sur­vival or reproduction.
Beauty may be determined by our visual expe­rience of our own local social and cultural envi­ronment. The faces we see share some common properties, characteristic for our ethnic group. We get used to those properties and check whether they can also be found within a strang­er’s face. Sociocultural factors inuence our judgment of those faces, e.g., watching a movie like Beauty and the Beast might inuence a child’s judgment on beauty and ugliness. If cer­tain properties of the face are associated with a higher social status or cultural or religious value, it may lead to a higher reproductive success. If there is no or only limited viability drawback, even a small reproductive advantage connected to
Female population has
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Natural selection by survival: Interocular distance has no influence on survival (or larger eyespan is even disadvantageous)
Wide eyespan genotype also
has property of suppressing
female meiotc drive gene
Next Generation: No male descendants from male flies with short interocular distance
221
X-chromosal meiotic driver which causes sperms with Y-chromosome
to degenerate
sexual selection:
No preference
regarding eyespan
Fig. 14.5 In stalk-eyed ies, a meiotic drive gene has
been identied. This meiotic drift causes sperms with Y-chromosome to degenerate. In this model, male ies with wide eyespan have the potential to suppress the mei-
a facial feature might be sufcient to elicit a higher frequency. This mechanism is called “cul­tural selection” and has, e.g., been discussed as another possible reason (apart from the founder effect) associated with a higher prevalence of albinism in Native American people [40].
Superimposition of images to nd an average face from a dened population was performed, e.g., by Perrett etal. [41], using vectorized out­lines from portrait photographs. However, they connected the faces to degrees of attractiveness judged by a number of observers, and with these data they were able to identify facial properties of more attractive subjects. They could, by exagger­ating the difference between the average face of
otic drift gene, those with a narrow interocular distance have not. Real stalk-eyed ies in addition exhibit sexual preference for large eyespan
all subjects and the average of the most attractive faces, create a “super-beauty.”
In contrast to beauty, facial disgurement frequently causes a feeling of disgust [42, 43]. To explain avoidant behavior with unhealthy or poisonous dishes or drinks with evolutionary biology is suggesting itself. Evolution biology would likewise provide an obvious explanation for the behavior of keeping a healthy distance to persons who exhibit signs of a contagious disease. However, any threatening exposition or phenotypic trait can be to the detriment of the organism by reducing the probability to survive or to reproduce, indifferent or even an advan­tage for an organism by surviving and by this
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Given population with
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variability in one feature (interocular distance).
Average face
Feature has no influence on
Natural selection by survival: Narrowed means less stereoscopic perception
Survivors (may also predominantly carry genes that determine preference of partner with wider interocular distance)
Fig. 14.6 Averageness as a result of evolution by “sur-
vival of the ttest.” In this example, a narrowed interocu­lar distance would be a drawback in spatial perception.
attractivity and
reproductive success
New average face
Another important factor for survival would be the induc­tion of parental care by cuteness
proving the higher qualication to survive, i.e., the “good genes.” In fact, even an obvious facial disgurement has been discussed as benecial from evolutionary biology’s perspective: Acne has been hypothesized as an evolutionary mechanism of protection while being at an immature age [44].
As a conclusion, it can be summarized that evolutionary biology gives good and reasonable explanations for many phenomena, but instead of simple chains of causation, it offers several mechanisms for the selection of facial properties, beauty, and disgurement. Some traits of the
human face may not have evolved by a process of adaptation but as a genetic by-product of another process. As long as not all factors and their inter­actions are understood, attempts to explain aspects of beauty of the human face by a simple chain of causation would be speculative.
14.3 Beauty andFacial Symmetry
In mathematical terms, symmetry is the property of an object to be invariant to certain transforma­tions: reection, rotation, scaling, and transla-
Given population with
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One variation (red hair) is
Natural selection Feature has no influence on survival
223
variability in one feature (color of hair).
Average face
predominantly chosen
as partner due to
increased attractivity
Survivors (may also predominantly carry genes that determine preference of red-haired partner)
Fig. 14.7 Averageness as a result of evolution by “repro-
ductive success of the most attractive.” In this example, red would be the most frequent color of hair (or nearly the “average” color) after a few generations. This mechanism
tion. The human face and the human body plan except for the internal organs are mirror symmet­ric. This is also true for most species of the ani­mal kingdom. Radial symmetry is found, e.g., in jellysh and starsh or in plants. In early animal life, bilateral symmetry of the body plan was probably advantageous for locomotion and was genetically xed for the whole body plan at an early stage of evolution. As a consequence, the detection of bilaterally or radially symmetrical structures was advantageous because it was a reliable strategy to detect plants and animals in the environment. This capability was necessary
New average face
would include genetically determined preferences in mate choice as well as preferences by sociocultural conventions
to nd predators, mates, or food. Visual percep­tion of bilateral and radial symmetry was studied, e.g., by Martinovic etal. [45] and Jennings and Kingdom [46].
In addition, translational transformation invari­ance, i.e., periodic structures, may occur in sights with regularly or irregularly repeating similar ele­ments, like a host of owers, a shoal of sh, a site with many mushrooms, or a tree full of fruit (Fig.14.9). Regular translation in two dimensions leads to characteristic areal patterns, e.g., sh scales. Realizing scaling symmetry might have been advantageous in pattern recognition and spa-