Function-dependent shape characteristics of the human skull

Using the FEM-program ANSYS 5.4, we have shaped a model of the human skull in which the flow of forces and the relative location and magnitudes of stresses are investigated. Forces are applied from below through the tooth row of the upper jaw. An ample volume is provided for the transmission of these bite forces upward to the roof of the braincase, where bearings counteract the forces from below. Within this volume, no other morphological features are considered than two cone-shaped orbits and a nasal channel which has a rounded, triangular cross section, extending upward between the orbits. Under loads (= bite forces) acting simultaneously in the directions and relative sizes of realistic bite- and chewing forces, there occurred stress concentrations inside the model which resemble closely the morphological characteristics of the human skull. The most remarkable pathways of stresses correspond to Toldt's and Benninghoff's nasal, zygomatic and pterygoid pillars. Aside from these stress concentrations, stress-free regions become visible at places, where the skull shows excavations: the vaulted palate with canalis incisivus, the canine fossa, superior and inferior orbital fissure, or cavities like the maxillary sinuses and cavum cranii. Behind the posterior molars and the pterygoid, the stresses disappear abruptly, and in the side wall of the nasal cavity a maxillary hiatus remains without stresses. A flow of forces comparable to, but not at the exact position of the zygomatic arch extends from the highly stressed zygomatic bone rearward and upward. In a later step of simulation, somewhat deeper, at the place of the really existing zygomatic arch, a series of small forces was applied, which correspond to the resultant force that is created by the redirection of the pull of the m. masseter into the temporal fascia. This--biologically reasonable--manipulation of the model leads to a reduction of the forces in the zygomatic bone, and to a downward shift of the zygomatic arch and its isolation from the skull's side wall by a deep, stress-free temporal fossa. The similarity between the stress flow in the model and the shape of the skull seems to indicate that the skull, like the bones of the postcranial skeleton, develops its shape in dependence from the mechanic stressing through the process of causal histogenesis. In view of experimental results, the possibility cannot be ruled out, that the safety factors in the skull deviate from those in the postcranial skeleton.     

Comparative finite element analysis of the cranial performance of four herbivorous marsupials

Marsupial herbivores exhibit a wide variety of skull shapes and sizes to exploit different ecological niches. Several studies on teeth, dentaries, and jaw adductor muscles indicate that marsupial herbivores exhibit different specializations for grazing and browsing. No studies, however, have examined the skulls of marsupial herbivores to determine the relationship between stress and strain, and the evolution of skull shape. The relationship between skull morphology, biomechanical performance, and diet was tested by applying the finite element method to the skulls of four marsupial herbivores: the common wombat (Vombatus ursinus), koala (Phascolarctos cinereus), swamp wallaby (Wallabia bicolor), and red kangaroo (Macropus rufus). It was hypothesized that grazers, requiring stronger skulls to process tougher food, would have higher biomechanical performance than browsers. This was true when comparing the koala and wallaby (browsers) to the wombat (a grazer). The cranial model of the wombat resulted in low stress and high mechanical efficiency in relation to a robust skull capable of generating high bite forces. However, the kangaroo, also a grazer, has evolved a very different strategy to process tough food. The cranium is much more gracile and has higher stress and lower mechanical efficiency, but they adopt a different method of processing food by having a curved tooth row to concentrate force in a smaller area and molar progression to remove worn teeth from the tooth row. Therefore, the position of the bite is crucial for the structural performance of the kangaroo skull, while it is not for the wombat which process food along the entire tooth row. In accordance with previous studies, the results from this study show the mammalian skull is optimized to resist forces generated during feeding. However, other factors, including the lifestyle of the animal and its environment, also affect selection for skull morphology to meet multiple functional demands. J. Morphol. 276:1230–1243, 2015. © 2015 Wiley Periodicals, Inc.     

Effects of gape and tooth position on bite force and skull stress in the dingo (Canis lupus dingo) using a 3-dimensional finite element approach

Models of the mammalian jaw have predicted that bite force is intimately linked to jaw gape and to tooth position. Despite widespread use, few empirical studies have provided evidence to validate these models in non-human mammals and none have considered the influence of gape angle on the distribution of stress. Here using a multi-property finite element (FE) model of Canis lupus dingo, we examined the influence of gape angle and bite point on both bite force and cranial stress. Bite force data in relation to jaw gape and along the tooth row, are in broad agreement with previously reported results. However stress data showed that the skull of C. l. dingo is mechanically suited to withstand stresses at wide gapes; a result that agreed well with previously held views regarding carnivoran evolution. Stress data, combined with bite force information, suggested that there is an optimal bite angle of between 25 degrees and 35 degrees in C. l. dingo. The function of these rather small bite angles remains unclear.     

腊玛古猿和西瓦古猿的形态特征及其系统关系——颅骨的形态与比较

本文通过具体的形态比较指出,禄丰腊玛古猿和西瓦古猿应为同一类型的雌雄个体,它们与现代猩猩比较相似,而与大猩猩和黑猩猩差别较大,因此,它们可看作是猩猩的祖先。猩猩这一支大约是在一千二百万年前开始从人猿超科的进化主干上分化出来的。     

Comparison between in vivo and theoretical bite performance: Using multi-body modelling to predict muscle and bite forces in a reptile skull

In biomechanical investigations, geometrically accurate computer models of anatomical structures can be created readily using computed-tomography scan images. However, representation of soft tissue structures is more challenging, relying on approximations to predict the muscle loading conditions that are essential in detailed functional analyses. Here, using a sophisticated multi-body computer model of a reptile skull (the rhynchocephalian Sphenodon), we assess the accuracy of muscle force predictions by comparing predicted bite forces against in vivo data. The model predicts a bite force almost three times lower than that measured experimentally. Peak muscle force estimates are highly sensitive to fibre length, muscle stress, and pennation where the angle is large, and variation in these parameters can generate substantial differences in predicted bite forces. A review of theoretical bite predictions amongst lizards reveals that bite forces are consistently underestimated, possibly because of high levels of muscle pennation in these animals. To generate realistic bites during theoretical analyses in Sphenodon, lizards, and related groups we suggest that standard muscle force calculations should be multiplied by a factor of up to three. We show that bite forces increase and joint forces decrease as the bite point shifts posteriorly within the jaw, with the most posterior bite location generating a bite force almost double that of the most anterior bite. Unilateral and bilateral bites produced similar total bite forces; however, the pressure exerted by the teeth is double during unilateral biting as the tooth contact area is reduced by half.     

Testing functional and morphological interpretations of enamel thickness along the deciduous tooth row in human children

The significance of a gradient in enamel thickness along the human permanent molar row has been debated in the literature. Some attribute increased enamel thickness from first to third molars to greater bite force during chewing. Others argue that thicker third molar enamel relates to a smaller crown size facilitated by a reduced dentin component. Thus, differences in morphology, not function, explains enamel thickness. This study draws on these different interpretive models to assess enamel thickness along the entire human deciduous tooth row. Average enamel thickness (AET), the area and proportion of crown enamel and dentin, and a crown size proxy are calculated for incisors, canines, and molars. Allometric scaling relationships are assessed within each tooth class, and then comparisons are undertaken along the row. Generally, AET was correlated with crown size and scaled with isometry, except for second molars which scaled with positive allometry. Mean AET increased along the row and was greater on molars, where bite forces are reported to be higher. Second molars combined the largest crown size with the thickest enamel and the smallest proportion of dentin, which is consistent with a reduction in the potential for cusp fracture under high bite forces. Resistance to wear may also account for some enamel thickness variation between tooth classes. Dental reduction did not explain the trend in AET from central to lateral incisors, or from first to second molars. The gradient in AET along the deciduous tooth row is partly consistent with a functional interpretation of enamel thickness. Am J Phys Anthropol 151:518–525, 2013. © 2013 Wiley Periodicals, Inc.     

The influence of feeding on the evolution of sensory signals: a comparative test of an evolutionary trade‐off between masticatory and sensory functions of skulls in southern African Horseshoe bats (Rhinolophidae)

The skulls of animals have to perform many functions. Optimization for one function may mean another function is less optimized, resulting in evolutionary trade‐offs. Here, we investigate whether a trade‐off exists between the masticatory and sensory functions of animal skulls using echolocating bats as model species. Several species of rhinolophid bats deviate from the allometric relationship between body size and echolocation frequency. Such deviation may be the result of selection for increased bite force, resulting in a decrease in snout length which could in turn lead to higher echolocation frequencies. If so, there should be a positive relationship between bite force and echolocation frequency. We investigated this relationship in several species of southern African rhinolophids using phylogenetically informed analyses of the allometry of their bite force and echolocation frequency and of the three‐dimensional shape of their skulls. As predicted, echolocation frequency was positively correlated with bite force, suggesting that its evolution is influenced by a trade‐off between the masticatory and sensory functions of the skull. In support of this, variation in skull shape was explained by both echolocation frequency (80%) and bite force (20%). Furthermore, it appears that selection has acted on the nasal capsules, which have a frequency‐specific impedance matching function during vocalization. There was a negative correlation between echolocation frequency and capsule volume across species. Optimization of the masticatory function of the skull may have been achieved through changes in the shape of the mandible and associated musculature, elements not considered in this study.     

New faces of Aegyptopithecus from the Oligocene of Egypt

Three recently discovered faces of Aegyptopithecus zeuxis from the Oligocene Jebel Qatrani Formation of Egypt provide new information about the shape and variation of the facial cranium, the earliest preserved for a presumed forerunner of apes and humans. Although varying considerably in details of shape and proportion, the new finds and a skull found in 1966 all appear to be of males, a conclusion based in part on the development of temporal and sagittal crests and on the large size of upper canines or their sockets (female canines are much smaller). The snouts of the three new faces all are shorter and broader than that of the earlier found skull as reconstructed. As in most later species of Anthropoidea, variation between these specimens is high.Aegyptopithecus helps define the nature of the oldest Anthropoidea and generally most resembles later-occurring apes. Many features, both derived and shared primitive, link Aegyptopithecus, the large Miocene great apes of the Proconsul group, and modern great apes. That these shared features and proportions are not direct allometric consequences of body size is indicated by Aegyptopithecus' resemblance to the large apes and its many distinctions from similar-sized Hylobates.In Aegyptopithecus brain volume scales smaller than in later catarrhines relative to facial size, the ectotympanic tube is less developed and the premaxilla is more primitive than in later higher primates. In closure of orbits and conformation of forehead, face and dentition, Aegyptopithecus closely resembles higher primates and not prosimians. Taken together, its overall cranial and dental anatomy constitutes one of the most important connecting links in primate evolutionary history.     

Implications of predatory specialization for cranial form and function in canids

The shape of the cranium varies widely among members of the order Carnivora, but the factors that drive the evolution of differences in shape remain unclear. Selection for increased bite force, bite speed or skull strength may all affect cranial morphology. We investigated the relationship between cranial form and function in the trophically diverse dog family, Canidae, using linear morphometrics and finite element (FE) analyses that simulated the internal and external forces that act on the skull during the act of prey capture and killing. In contrast to previous FE-based studies, we compared models using a newly developed method that removes the effects of size and highlights the relationship between shape and performance. Cranial shape varies among canids based on diet, and different selective forces presumably drove evolution of these phenotypes. The long, narrow jaws of small prey specialists appear to reflect selection for fast jaw closure at the expense of bite force. Generalists have intermediate jaw dimensions and produce moderate bite forces, but their crania are comparable in strength to those of small prey specialists. Canids that take large prey have short, broad jaws, produce the largest bite forces and possess very strong crania. Our FE simulations suggest that the remarkable strength of skulls of large prey specialists reflect the additional ability to resist extrinsic loads that may be encountered while struggling with large prey items.     

The impact of digging on craniodental morphology and integration

The relationship between the form and function of the skull has been the subject of a great deal of research, much of which has concentrated on the impact of feeding on skull shape. However, there are a number of other behaviours that can influence craniodental morphology. Previous work has shown that subterranean rodents that use their incisors to dig (chisel‐tooth digging) have a constrained cranial shape, which is probably driven by a necessity to create high bite forces at wide gapes. Chisel‐tooth‐digging rodents also have an upper incisor root that is displaced further back into the cranium compared with other rodents. This study quantified cranial shape and upper incisors of a phylogenetically diverse sample of rodents to determine if chisel‐tooth‐digging rodents differ in craniodental morphology. The study showed that the crania of chisel‐tooth‐digging rodents shared a similar place in morphospace, but a strong phylogenetic signal within the sample meant that this grouping was nonsignificant. It was also found that the curvature of the upper incisor in chisel‐tooth diggers was significantly larger than in other rodents. Interestingly, most subterranean rodents in the sample (both chisel‐tooth and scratch diggers) had upper incisors that were better able to resist bending than those of terrestrial rodents, presumably due to their similar diets of tough plant materials. Finally, the incisor variables and cranial shape were not found to covary consistently in this sample, highlighting the complex relationship between a species’ evolutionary history and functional morphology.     

Mechanical structure and function of the craniofacial skeleton of the domestic dog.

Masticatory habit is a major factor determining the morphology of the craniofacial skeleton. The craniofacial skeleton essentially comprises a series of bony stress-bearing bridges forming a structural framework. The structural framework of the skull of dog has been described as a rigid trestle-like structure; it can be illustrated by mechanically removing nonresistant areas of bone. It is then found that a framework is produced which is partially rigid (cranium) and partly flexible (rostrum). It is postulated that the flexibility of the rostrum acts to absorb shock and it is suggested that the primate postorbital bar is developed in response to craniofacial morphology which increases compressive bite forces.     

Functional constraints on tooth morphology in carnivorous mammals

ABSTRACT: BACKGROUND: The range of potential morphologies resulting from evolution is limited by complex interacting processes, ranging from development to function. Quantifying these interactions is important for understanding adaptation and convergent evolution. Using three-dimensional reconstructions of carnivoran and dasyuromorph tooth rows, we compared statistical models of the relationship between tooth row shape and the opposing tooth row, a static feature, as well as measures of mandibular motion during chewing (occlusion), which are kinetic features. This is a new approach to quantifying functional integration because we use measures of movement and displacement, such as the amount the mandible translates laterally during occlusion, as opposed to conventional morphological measures, such as mandible length and geometric landmarks. By sampling two distantly related groups of ecologically similar mammals, we study carnivorous mammals in general rather than a specific group of mammals. RESULTS: Statistical model comparisons demonstrate that the best performing models always include some measure of mandibular motion, indicating that functional and statistical models of tooth shape as purely a function of the opposing tooth row are too simple and that increased model complexity provides a better understanding of tooth form. The predictors of the best performing models always included the opposing tooth row shape and a relative linear measure of mandibular motion. CONCLUSIONS: Our results provide quantitative support of long-standing hypotheses of tooth row shape as being influenced by mandibular motion in addition to the opposing tooth row. Additionally, this study illustrates the utility and necessity of including kinetic features in analyses of morphological integration.     

Of arcs and vaults: the biomechanics of bone‐cracking in spotted hyenas (Crocuta crocuta)

The ability to break open large bones has evolved independently in only three groups of carnivorous mammals, all of which have robust teeth, vaulted foreheads, and pronounced sagittal crests. One unusual skull feature, present in bone‐cracking members of the family Hyaenidae, is a caudally elongated frontal sinus, hypothesized to function in resistance to bending and stress dissipation during bone‐cracking. In the present study, we used finite element (FE) analysis to examine patterns of stress distribution in the spotted hyena (Crocuta crocuta) skull during unilateral biting, and inquire about the functional role of the fronto‐parietal sinus in stress dissipation. We constructed and compared three FE models: (1) a ‘normal’ model of an adult Crocuta skull; (2) a model in which the caudal portion of the fronto‐parietal sinus was filled with bone; and (3) a model in which we flattened the sagittal crest to resemble the plate‐like crests of other mammals. During biting, an arc of stress extends from the bite point up through the vaulted forehead and along the sagittal crest. Our results suggest that pneumatization of the hyena's skull both enhances its ability to resist bending and, together with the vaulted forehead, plays a critical role in evenly dissipating stress away from the facial region. © 2008 The Linnean Society of London, Biological Journal of the Linnean Society, 2008, 95 , 246–255.     

The growth of the skull and jaw muscles and its functional consequences in the New Zealand rabbit (Oryctolagus cuniculus)

Between weaning and adulthood, the length and height of the facial skull of the New Zealand rabbit (Oryctolagus cuniculus) double, whereas much less growth occurs in the width of the face and in the neurocranium. There is a five-fold increase in mass of the masticatory muscles, caused mainly by growth in cross-sectional area. The share of the superficial masseter in the total mass increases at the cost of the jaw openers. There are changes in the direction of the working lines of a few muscles. A 3-dimensional mechanical model was used to predict bite forces at different mandibular positions. It shows that young rabbits are able to generate large bite forces at a wider range of mandibular positions than adults and that the forces are directed more vertically. In young and adult animals, the masticatory muscles differ from each other with respect to the degree of gape at which optimum sarcomere length is reached. Consequently, bite force can be maintained over a range of gapes, larger than predicted on basis of individual length-tension curves. Despite the considerable changes in skull shape and concurrent changes in the jaw muscles, the direction of the resultant force of the closing muscles and its mechanical advantage remain stable during growth. Observed phenomena suggest that during development the possibilities for generation of large bite forces are increased at the cost of a restriction of the range of jaw excursion.     

Tooth root morphology as an indicator for dietary specialization in carnivores (Mammalia: Carnivora)

The Carnivora occupy a wide range of feeding niches in concordance with the enormous diversity in their skull and dental form. It is well established that differences in crown morphology are linked to variations in the material properties of the foods ingested and masticated. However, how tooth root form is related to dietary specialization is less well known. In the present study, we investigate the relationship between tooth root morphology and dietary specialization in terrestrial carnivores (canids, felids, hyaenids, and ursids). We specifically address the question of how variation in tooth root surface area is related to bite force potentials as one of the crucial masticatory performance parameters in feeding ecology. We applied computed tomography imaging to reconstruct and quantify dental root surface area in 17 extant carnivore species. Moreover, we computed maximal bite force at several tooth positions based on a dry skull model and assessed the relationship of root surface area to skull size, maximal bite force, food properties, and prey size. We found that postcanine tooth root surface areas corrected for skull size serve as a proxy for bite force potentials and, by extension, dietary specialization in carnivores. Irrespective of taxonomic affinity, species that feed on hard food objects have larger tooth roots than those that eat soft or tough foods. Moreover, carnivores that prey on large animals have larger tooth root surface areas. Our results show that tooth root morphology is a useful indicator of bite force production and allows inferences to be made about dietary ecology in both extant and extinct mammals. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, 105, 456–471.     

Evolution of skull and mandible shape in cats (Carnivora: Felidae)

The felid family consists of two major subgroups, the sabretoothed and the feline cats, to which all extant species belong, and are the most anatomically derived of all carnivores for predation on large prey with a precision killing bite. There has been much controversy and uncertainty about why the skulls and mandibles of sabretoothed and feline cats evolved to become so anatomically divergent, but previous models have focused on single characters and no unifying hypothesis of evolutionary shape changes has been formulated. Here I show that the shape of the skull and mandible in derived sabrecats occupy entirely different positions within overall morphospace from feline cats, and that the evolution of skull and mandible shape has followed very different paths in the two subgroups. When normalised for body-size differences, evolution of bite forces differ markedly in the two groups, and are much lower in derived sabrecats, and they show a significant relationship with size and cranial shape, whereas no such relationship is present in feline cats. Evolution of skull and mandible shape in modern cats has been governed by the need for uniform powerful biting irrespective of body size, whereas in sabrecats, shape evolution was governed by selective pressures for efficient predation with hypertrophied upper canines at high gape angles, and bite forces were secondary and became progressively weaker during sabrecat evolution. The current study emphasises combinations of new techniques for morphological shape analysis and biomechanical studies to formulate evolutionary hypotheses for difficult groups.     

Scaling relationships within the maxillary tooth row of the Felidae, and the absence of the second upper premolar in Lynx

Suggestions that short-faced members of the Felidae tend to lack the second upper premolar (P2) imply a possible shift in scaling associated with the palate and maxillary tooth row in Lynx , which lacks P2, as compared to felids that retain it. This hypothesis is tested using a scaling model that relates the lengths of the palate, and the upper tooth row and its components, to post-palatal skull length in the small to moderately large felids Felis catus (domestic cat), L. canadensis (Canada lynx), F. pardalis (ocelot), and F. concolor (cougar). Scaling relationships of both palate and tooth row length to post-palatal skull length do not differ significantly from isometry in all four species. However, ocelots have a significantly shorter palate and tooth row than lynxes over their overlapping ranges of post-palatal skull length, suggesting that the absence of P2 is not correlated with the length of the face in these species. CI, P3 and P4 tend to be relatively longer in larger felids; none the less, ocelots have a relatively small P3 and lynxes have a proportionately large P4. Because both lynxes and ocelots have a relatively small gap between CI and P3, the absence of P2 is not correlated with available space within the tooth row in adults. However, lynxes also appear to have a relatively long dP3 that almost obliterates the diastema within the deciduous tooth row. The absence of P2 in Lynx may be an engineering artefact that is associated with a shift in proportions within the deciduous toothrow, resulting in inhibition of the development of P2 and dP2 early in ontogeny. Despite the variable occurrence and polymorphism associated with P2 in the Felidae, this character has systematic value within this clade and is a synapomorphy for Lynx.     

Mosaic functionality in a transitional ecomorphology: skull biomechanics in stem Hyaeninae compared to modern South African carnivorans

Ecomorphologies are categories of ecological adaptation and function, although intermediates are not always available to shed light on functionality at the transitional stages between them. We examined an intermediate bone‐cracking carnivoran ecomorphology, the stem hyaenine Ikelohyaena abronia, using finite element analysis. Skull models of Ikelohyaena, crown hyaenine Crocuta crocuta, and two other hypercarnivores were simulated with mastication and prey apprehension forces. The results obtained show that Ikelohyaena already possessed derived features in skull stress distribution and levels of strain energy, characteristic of the extant bone‐cracking Crocuta; however, the estimated bite forces in Ikelohyaena were significantly lower. Prey apprehension simulations showed similar patterns; the low skull strain energy and low bite force of the Ikelohyaena mandible indicate a poor individual ability to take down large prey. The mosaic features of craniodental function in Ikelohyaena suggest that initial evolution of the hyaenid bone‐cracking ecomorphology involved skull shape changes that increased stress dissipation, permitting incorporation of more hard food into the diet. Subsequent evolution of larger bite forces was then required to increase the size limit of bones that can be cracked and consumed. This mode of evolution would have allowed transitional hyaenid ecomorphologies to continuously increase the carcass processing ability both during competitive feeding and scavenging throughout their evolution. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 102 , 540–559.     

The biomechanical consequences of longirostry in crocodilians and odontocetes

Unrelated clades of aquatic tetrapod have evolved a similar range of skull shapes, varying from longirostrine (elongate and narrow rostrum) to brevirostrine (short rostrum). However, it is unclear which aspects of organismal performance are associated with this convergence in the range of skull shapes. Furthermore, it is not known how fundamental anatomical differences between groups influence these relationships. Here we address this by examining the load bearing capabilities of the skulls of two of the most diverse groups of living aquatic tetrapod: crocodilians and odontocetes. We use finite element analysis to examine the abilities of different cranial morphologies to resist a range of biologically relevant feeding loads including biting, shaking and twisting. The results allow for form/function relationships to be compared and contrasted between the two groups. We find that cranial shape has similar influences on performance during biting, shaking or twisting load cases at the anterior tooth positions, e.g. brevirostrine species experienced less strain than longirostrine species. The pattern of this form/function relationship is similar for both crocodilians and odontocetes, despite their fundamentally different anatomies. However, when loading teeth at the posterior end or middle of the tooth row the results do not follow the same pattern. Behavioural differences in bite location plays a key role in determining functional abilities in aquatic tetrapod taxa.     

The role of the zygomatic arch in the statics of the skull and its adaptive shape

The zygomatic arch of mammals is usually considered a phylogenetic relic of the fenestrations of the skull roof which may be observed in morphological sequences of primitive vertebrate skulls. If this concept is correct, the element is comparable (though not homologous) to the jugal arches of diapsid reptiles. Two major questions then remain unanswered: why different elements are maintained in reptiles and mammals during evolution, and why the arches are maintained as relics of ancestral forms. It is tempting to respond to the latter question with a very simple answer, namely that the elements function in order to sustain mechanical stresses. In this paper, we raise the questions which quality of stresses occurs in a primate skull within the zygomatic arches and what relationship these stresses hold to the morphology of these bony elements. An answer has been sought by means of finite element stress analysis. We found that the zygomatic arch in primate skulls represents a structure which carries, under all biologically relevant conditions, either compressive or tensile stresses. In a very simple model of the human skull under bite forces, a strip of stresses occurs lateral to the orbits, which seems roughly comparable to the zygomatic arch. Once such a structure exists and is used as an insertion of adductor muscles, it will be exposed to bending stress in side view and in frontal view. Morphological details of the zygomatic arch (curvature, profile, suture) are well suited to sustain the evoked stresses by a minimum of material.