Search

Surgical accesses through the middle cranial fossa (MCF) and their variations require the surgeons a detailed understanding of a complex anatomy of this site of the inner base of the skull (IBS) and an individual anatomical variability of the anatomical landmarks often used in their medical practice. The aim of this study is to establish individual anatomical variability of the longitudinal dimensions of MCF of mature age human. The research was carried out by studying 50 craniotomograms and 50 bone preparations of mature age human skulls with their further subdivision to extreme types of skulls groups. The examinations of the main longitudinal parameters were done for detailed MCF craniometry, namely: MCF lateral cranial length, MCF general length, MCF medial areas length. It was determined that all longitudinal dimensions increase from brachicephales to dolichocephales. This is due to the fact that for brachicrans (round-headedness) short form of the skull is inherent, for dolichocrans (narrow-headedness) – long and for mesocrans (moderate-headedness) average head size is inherent. According to the received data, MCF longitudinal parameters of mature age human regardless of the extreme types of the skull structure have the tendency to increase from medial sections of the investigated area to lateral. The results of this study substantially complete the existing information about the individual anatomical variability of MCF of mature age human and also make it possible to deeply use this data in practical medicine and for further research in morphology and in craniology in details.

Background The range of normal variation of growth and development of the craniofacial region is of direct clinical interest but incompletely understood. Here we develop a statistical model of craniofacial growth and development to compare craniofacial ontogeny between age groups and sexes and pilot an approach to modeling that is relatively straightforward to apply in the context of clinical research and assessment. Methods The sample comprises head surface meshes captured using a 3dMD five-camera system from 65 males and 47 females (range 3-20 years) from the Headspace project, Liverpool, UK. The surface meshes were parameterized using 16 anatomical landmarks and 59 semilandmarks on curves and surfaces. Modes and degrees of growth and development were assessed and compared among ages and sexes using Procrustes based geometric morphometric methods. Results Regression analyses indicate that 3-10 year olds undergo greater changes than 11-20 year olds and that craniofacial growth and development differs between these age groups. The analyses indicate that males extend growth allometrically into larger size ranges, contributing substantially to adult dimorphism. Comparisons of ontogenetic trajectories between sexes find no significant differences, yet when hypermorphosis is accounted for in the older age group there is a significant residual sexual dimorphism. Conclusions The study adds to knowledge of how adult craniofacial form and sexual dimorphism develop. It was carried out using readily available software which facilitates replication of this work in diverse populations to underpin clinical assessment of deformity and the outcomes of corrective interventions.

Cranial bones of the plesiosaurus Abyssosaurus nataliae Berezin, 2011 from the Upper Hauterivian (Lower Cretaceous) of Chuvashia are described. It differs from other known Cryptoclididae in the evident pedomorphic characters in the skull structure. The skull is strongly hypertrophic; the visceral part is shortened relative to its large occipital region; the orbits are enlarged, the lower jaw is narrow. The jugal is well developed, positioned vertically, and borders most of the posterior orbital wall. This skull structure is evidence of deepwater mode of life. The species diagnosis is revised.

This article explores the importance of the Derbyshire antiquarian Thomas Bateman in the context of mid-nineteenth-century debates about ethnology, craniology, and archaeological chronology. New information on the relationship between Bateman and the authors ofCrania Britannica, Joseph Barnard Davis and John Thurnam, is brought to light thanks to unpublished archival material from the Sheffield Museums and the Royal Anthropological Institute.Crania Britannicawas the first publication of British national skull types from prehistory to the Anglo-Saxon period. The publication employed the techniques of craniology—the systematic study of head types—as a chronological tool. Indeed, craniology is often seen as the mechanism by which the Three Age System was initially received in Britain and Ireland. Here, Bateman's involvement in the publication and his own theories on the development of the past with regard to cranial sequencing and archaeological chronology are explored in greater detail.

Objectives: We examine how dental sexual dimorphism develops in mandrills, an extremely sexually dimorphic primate. We aimed to (a) establish the chronology of dental development (odontochronology) in male and female mandrills, (b) understand interindividual and intersex variation in odontochronologies, and (c) determine how dental sexual dimorphism is achieved. Materials and Methods: We prepared histological ground sections from the permanent teeth of four female and four male mandrills from the semi‐free ranging colony at the Centre International de Recherches Medicales, Franceville, Gabon. We used the microscopic growth increments in the sections to create odontochronologies. We compared ages at crown initiation, crown formation times (CFT) and crown extension rates (CER) between individuals and sexes to assess interindividual and intersex variation. Results: All mandrill teeth are sexually dimorphic in size. Dental sexual dimorphism in mandrills is achieved via sex differences in the duration of growth (bimaturism) and in growth rates. We also found interindividual and intersex variation in the ages at initiation and completion of crown formation. Discussion: Our results show that the rate of ameloblast differentiation varies between individuals and that selection for both the age at tooth initiation and CER has occurred independently in males and females to ensure that the teeth develop at appropriate times relative to the growth of the sexually dimorphic jaws. They also show that canine dimorphism is achieved through differences in both CER and CFT, unlike extant great apes or Cantius . Given at least three mechanisms for achieving canine dimorphism, we need more information to trace the evolution of this trait in primates.

With tooth attrition, the height of the alveolar crest does not increase to keep pace with active tooth eruption and the cemento-enamel junction-alveolar crest distance increases slightly with age in aboriginal skulls. But there is no atrophy of the alveolar bony margin. Some decrease in interalveolar height does occur. This does not necessarily mean that passive eruption with exposure of cementum is normal. Rather it is postulated that the epithelial attachment proliferates onto cementum, inhibiting alveolar crest addition, while the base of the gingival sulcus remains at the cemento-enamel junction. During the course of this investigation, it was found that the distance between the cemento-enamel junction and alveolar crest increased more rapidly with advancing wear in the lower molar region than in the upper. In the lower first molar region, the lingual distance was significantly greater than that between cemento-enamel junction and alveolar crest on the buccal aspect during each stage of wear. The size of the tooth, as reflected in the robustness index, had no influence on the processes or rate of active eruption, bone deposition at the alveolar crest, or measurements taken between cemento-enamel junction and alveolar crest.

Generalized scheme for description of craniometric characters of mammals is presented, with detailed analysis of each group of signs (overall, braincase, rostrum, and mandible). Unified system of acronyms for designation of measurements is proposed and applied. Partial schemes are presented, separately for each typical representative of main orders known in the fauna of Ukraine: rodents (Sylvaemus), bats (Eptesicus), insectivores (Crocidura), carnivores (Mustela), ungulates (Capreolus). All partial schemes are illustrated by photos with designations of key points for measurements. Each partial scheme includes about 15–20 metric features. Problems of “excess”, small-sized and group-specific features as well as size of samples are discussed. The application of description of craniometric variation was considered: diagnostics of closed species, differentiation of age and sex groups, analysis of geographic variation, growth changes of features, study of evolutional and ecomorphological differentiation of species etc.

A statistical analysis of measurements of crania from the 2nd and 3rd century AD cemetery at Beniamin, Armenia, indicates considerable morphological heterogeneity. Between-group comparisons reveal affinities between the Beniamin people and Scythians of the North Pontic region, the Sarmatians of the Volga–Ural region, and the Sacae of Western Central Asia. The results attest to intense migrations of nomads to Transcaucasia during Classical Antiquity and to the ethnic diversity of the Caucasian populations.

There has been a protracted debate over the evidence for intentional cranial modification in the terminal Pleistocene Australian crania from Kow Swamp and Coobool Creek. Resolution of this debate is crucial to interpretations of the significance of morphological variation within terminal Pleistocene-early Holocene Australian skeletal materials and claims of a regional evolutionary sequence linking Javan Homo erectus and Australian Homo sapiens. However, morphological comparisons of terminal Pleistocene and recent Australian crania are complicated by the significantly greater average body mass in the former. Raw and size-adjusted metric comparisons of the terminal Pleistocene skeleton from Nacurrie, south-eastern Australia, with modified and unmodified H. sapiens and H. erectus, identified a suite of traits in the frontal, parietal, and occipital bones associated with intentional modification of a neonate's skull. These traits are also present in some of the crania from Kow Swamp and Coobool Creek, which are in close geographic proximity to Nacurrie, but not in unmodified H. sapiens or Javan H. erectus. Frontal bone morphology in H. erectus was distinct from all of the Australian H. sapiens samples. During the first six months of life, Nacurrie's vault may have been shaped by his mother's hands, rather than though the application of fixed bandages. Whether this behaviour persisted only for several generations, or hundreds of years, remains unknown. The reasons behind the shaping of Nacurrie's head, aesthetics or otherwise, and why this cultural practice was adopted and subsequently discontinued, will always remain a matter of speculation.

Understanding the importance of environmental dimensions behind the morphological variation among populations has long been a central goal of evolutionary biology. The main objective of this study was to review the spatial regression techniques employed to test the association between morphological and environmental variables. In addition, we show empirically how spatial regression techniques can be used to test the association of cranial form variation among worldwide human populations with a set of ecological variables, taking into account the spatial autocorrelation in data. We suggest that spatial autocorrelation must be studied to explore the spatial structure underlying morphological variation and incorporated in regression models to provide more accurate statistical estimates of the relationships between morphological and ecological variables. Finally, we discuss the statistical properties of these techniques and the underlying reasons for using the spatial approach in population studies.

The interpretation of patterns of cranial pneumatization in terms of evolution, development, and function is controversial, because these structures exhibit extreme diversity and variability among and within taxa. However, there is general consensus that air-filled spaces are formed by invasion of mucous epithelial tissue from the nasopharyngeal cavity into the surrounding cranial bones. This investigation presents a morphogenetic model of pneumatization, which combines empirical data about epithelial growth with physical concepts of surface growth. The study develops a model that defines growth equations with a minimum number of system parameters to simulate the invasion of mucous tissue and air-filled spaces into the cancellous compartment of cranial bones. Computer simulations show that tuning a small set of model parameters permits generation of a wide diversity of morphologies mimicking natural air-filled spaces. Comparison of virtual with actual morphologies yields new insights into possible factors controlling the process of cranial pneumatization.

The cranial base is one of the major foci of interest in functional craniology. The evolution and morphogenesis of this structure are still poorly known and rather controversial because of multifactorial influences and polyphasic stages. Endocranial dynamics are associated anteriorly with the upper facial structures, laterally with the mandibular system and midsagittally with brain development. In the present study, we investigated the endocranial morphology of modern humans using 3D landmark-based approaches, i.e. geometric morphometrics and Euclidean distance matrix analysis. The structure of endocranial variation is poorly integrated, with only weak reciprocal influences among the three fossae. Some major variations are associated with changes in the posterior fossa, with possible consequences on the anterior areas. These main patterns of integration are hypothesized to be influenced by the connective tensors of the dura layers. Static allometry and sex differences are largely related to the ontogenetic sequences, characterized by early maturation of the anterior fossa with respect to the middle and posterior regions (i.e., relatively shorter posterior part of the planum sphenoideum and vertical lengthening of the clivus in males). The relative independence between the endocranial fossae, as well as their structural connection through the meningeal tensors, must be carefully considered in studies on the evolutionary dynamics, since they lead to mosaic changes through phylogeny.

In a recent study we found that crania from South Amerindian populations on each side of the Andes differ significantly in terms of craniofacial shape. Western populations formed one morphological group, distributed continuously over 14,000 km from the Fuegian archipelago (southern Chile) to the Zulia region (northwestern Venezuela). Easterners formed another group, distributed from the Atlantic Coast up to the eastern foothills of the Andes. This differentiation is further supported by several genetic studies, and indirectly by ecological and archaeological studies. Some authors suggest that this dual biological pattern is consistent with differential rates of gene flow and genetic drift operating on both sides of the Cordillera due to historical reasons. Here we show that such East-West patterning is also observable in North America. We suggest that the "ecological zones model" proposed by Dixon, explaining the spread of the early Americans along a Pacific dispersal corridor, combined with the evolution of different population dynamics in both regions, is the most parsimonious mechanism to explain the observed patterns of within- and between-group craniofacial variability. Fil: Pucciarelli, Hector Mario. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Departamento de Antropología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; Argentina Fil: González José, Rolando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Centro Nacional Patagónico. Instituto Patagónico de Ciencias Sociales y Humanas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Neves, Walter A.. Universidade de Sao Paulo; Brasil Fil: Sardi, Marina Laura. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Departamento de Antropología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; Argentina Fil: Rozzi, Fernando Ramírez. Centre National de la Recherche Scientifique; Francia

This paper discusses how the evolving hominid architecture of the arteriovenous system through the cranial base diverted foreseeable pathology in the human brain. Bipedal upright posture was an early adaptation in mosaic morphological pattern changes in hominid evolution; a key feature, the ability of blood to flow either to vertebral or internal jugular venous systems. Encephalization punctuated hominid evolution, its vulnerable feature, a lower threshold for thermal damage. Comparative analysis of ape and human skulls show “fingerprint” structures, revealing big changes in pattern complexity of the cranial vascular tree. Clues to structural/functional changes span data for apes, humans, and hominid fossils. Here, the increasing vascular network, Australopithecus to Homo sapiens, necessitated changes in the blood flow patterns. The transverse-sigmoid (T/S) and occipital-marginal (O/M) venous networks accommodated hydrostatic changes of blood flow, regulating temperature uniquely: the O/M system enlarged, allowing blood to flow straight down into the vertebral plexus without cooling, and added a vast network of emissary/diploic veins, acting as a brain cooling “radiator.” This O/M system was fixed in the Australopithecus robustus lineage, p = 0.000001; high frequencies of emissary foramen were selected for over time. Ontologically, the human neonatal O/M system is fully developed; emissary/diploic veins are established by age 5, setting conditions for selective brain cooling. The Radiator Theory is the evolution of the functionally efficient brain cooling system, fixed in the A. robustus lineage, tying hydrostatic consequences of bipedalism with release of a “thermal constraint” on the encephalizing brain, and reflected in our own ontogeny.

A GLIMPSE INTO MODERN PALEOANTHROPOLOGY: In the last decades, paleoanthropology has been deeply modified, changing from a descriptive and historical science to a more quantitative and analytical discipline. The covariation of multiple traits is investigated to study the evolutionary changes of the underlying anatomical models, mostly through the introduction of digital biomedical imaging procedures and of computed geometrical analyses supported by multivariate statistics. FUNCTIONAL CRANIOLOGY: The evolution of the human cranium is consequently considered in terms of functional and structural relationships between its components, largely influenced by the allometric variations associated with the increase in the relative cranial capacity. In the human genus, the changes in the face, base, and neurocranium are characterised by a mosaic variation, in which adaptations, secondary consequences, and stochastic factors concur to generate a set of anatomical possibilities and constraints. SYSTEMIC PERSPECTIVES TO THE EVOLUTION OF THE HUMAN CRANIAL MORPHOLOGY: Concepts like morphological modularity, anatomical integration, and heterochrony represent key issues in the development of the current human evolutionary studies.

International audience; Kenya National Museums Lukenya Hill Hominid 1 (KNM-LH 1) is a Homo sapiens partial calvaria from site GvJm-22 at Lukenya Hill, Kenya, associated with Later Stone Age (LSA) archaeological deposits. KNM-LH 1 is securely dated to the Late Pleistocene, and samples a time and region important for understanding the origins of modern human diversity. A revised chronology based on 26 accelerator mass spectrometry radiocarbon dates on ostrich eggshells indicates an age range of 23,576-22,887 y B.P. for KNM-LH 1, confirming prior attribution to the Last Glacial Maximum. Additional dates extend the maximum age for archaeological deposits at GvJm-22 to > 46,000 y B.P. (> 46 kya). These dates are consistent with new analyses identifying both Middle Stone Age and LSA lithic technologies at the site, making GvJm-22 a rare eastern African record of major human behavioral shifts during the Late Pleistocene. Comparative morphometric analyses of the KNM-LH 1 cranium document the temporal and spatial complexity of early modern human morphological variability. Features of cranial shape distinguish KNM-LH 1 and other Middle and Late Pleistocene African fossils from crania of recent Africans and samples from Holocene LSA and European Upper Paleolithic sites.

Brain size increased greatly during Pleistocene human evolution, while overall facial and dentognathic size decreased markedly. This mosaic pattern is due to either selective forces that acted uniquely on each functional unit in a modularized, developmentally uncoupled craniofacial complex, or alternatively, selection that acted primarily on one unit, with the other responding passively as part of a coevolved set of ontogenetically and evolutionarily integrated structures. Using conditional independence modeling on homologous linear measurements of the height, breadth, and depth of the cranium in Pan (n = 95), Gorilla (n = 102), and recent Homo (n = 120), we reject the null hypothesis of equal levels of overall cranial integration. While all three groups share the pattern of greater neurocranial integration with distinct separation between the face and neurocranium (modularization), family differences do exist. The apes are more integrated in their entire crania, but display a particularly strong pattern of integration within the facial complex related to prognathism. Modern humans display virtually no facial integration, a pattern which is likely related to their markedly decreased facial projection. Modern humans also differ from their great ape counterparts in being more integrated within the breadth dimension of the cranial vault, likely tied to the increase in brain size and eventual globularity seen in human evolution. That the modern human integration pattern differs from the ancestral African great ape pattern along the inverse neurocranial-facial trend seen in human evolution indicates that this shift in the pattern of integration is evolutionarily significant, and may help to clarify aspects of the current debate over defining modern humans.

Forensic pathologists may be asked to identify the ethnic group and gender of a cranium of unknown origin. An analysis of the maxillary sinus--its volume, shape, and dimensions in dried crania of different ethnic and gender groups (European and Zulu male and female)--was conducted to establish a new approach. A variation in maxillary sinus volume may mean a variation in anatomic landmarks between the groups. Ethnic and gender variations in the shape of the maxillary sinus of the crania were investigated. This research was further extended to predict the gender and ethnic group from an unknown cranium to make this research valuable to the fields of forensic pathology and anthropology. Helical, multislice computed tomography was performed using 1-mm coronal slices. The area for each slice was obtained by tracing the outline of each slice. The computed tomographic machine calculated a volume by totalling the slices for each sinus. Advanced computer methodology including a neural network was designed and applied to search for classification patterns in data. A discriminant analysis was performed to improve classification results. Ethnic and gender variations were found in the different groups, and the predictive role of the maxillary sinus in ethnic classification was established. It was found that European crania had significantly larger antral volumes than Zulu crania, and males had larger volumes than females. Dimensions of European sinuses were larger than those of Zulu sinuses. The medial antral wall of the sinus allowed for ethnic classification. The discriminant analysis allowed for a very successful 90% ethnic prediction, while gender prediction was ultimately 79%. The measurements taken and the formulae created in this research will be valuable to those in the field who are seeking to ethnically classify a cranium into one or another ethic group. This research aims to be an aid in identification, as well as a starting point for other scientific studies based on other ethnic groups. Perhaps its true value will lie in confirming ethnicity by adding to existing criteria. It must be noted that this classification is based on actual measurements and therefore eliminates the some of the subjectivity present in current methods of ethnic classification.

Neandertal faces have been described as being derived with respect to their overall length or degree of anterior projection. A comparison of cranial and mandibular indicators of lower facial projection across archaic and modern Homo indicates that Neandertal facial lengths on average are similar to those of preceding archaic Homo and principally contrast with those of recent humans. Neandertal facial length is not derived. The shortness of recent human facial skeletons is the evolutionarily derived condition.

This study investigates whether macaques and humans possess a common pattern of relative growth during the fetal period. The fetal samples consist of 16 male pigtailed macaques (mean age, 20.5 gestational weeks) and 17 humans (9 males and 8 females; mean age, 29.5 gestational weeks). For each individual, three-dimensional coordinates of 18 landmarks on the skull were collected from three-dimensional computed tomographic (CT) reconstructed images and two-dimensional CT axial slices. Early and late groups were created from the human (early mean age, 24 weeks, N = 8; late mean age, 34 weeks, N = 9) and macaque samples (early mean age, 17.7 weeks, N = 7; late mean age, 23 weeks, N = 9). Inter- and intraspecific comparisons were made between the early and late groups. To determine if macaques and humans share a common fetal pattern of relative growth, human change in shape estimated from a comparison of early and late groups was compared to the pattern estimated between early and late macaque groups. Euclidean distance matrix analysis was used in all comparisons. Intraspecific comparisons indicate that the growing fetal skull displays the greatest amount of change along mediolateral dimensions. Changes during human growth are primarily localized to the basicranium and palate, while macaques experience localized change in the midface. Interspecific comparisons indicate that the two primate species do not share a common pattern of relative growth, and the macaque pattern is characterized by increased midfacial growth relative to humans. Our results suggest that morphological differences in the craniofacial skeleton of these species are in part established by differences in fetal growth patterns.

The temporal bone is the location of sev- eral traits thought to differentiate Neanderthals from modern humans, including some proposed Neanderthal- derived traits. Most of these, however, are difficult to measure and are usually described qualitatively. This study applied the techniques of geometric morphometrics to the complex morphology of the temporal bone, in order to quantify the differences observed between Neanderthal and modern human anatomy. Two hundred and seventy modern human crania were measured, representing 9 populations of 30 individuals each, and spanning the ex- tremes of the modern human geographical range. Twelve Neanderthal specimens, as well as Reilingen, Kabwe, Skhul 5, Qafzeh 9, and 4 Late Paleolithic European spec- imens, were included in the fossil sample. The data were collected in the form of three-dimensional (3-D) landmark coordinates, and specimen configurations were superim- posed using generalized Procrustes analysis. The fitted coordinates were then analyzed by an array of multivari- ate statistical methods, including principal components analysis, canonical variates analysis, and Mahalanobis D 2 . The temporal bone landmark analysis was very suc- cessful in separating Neanderthals from modern humans. Neanderthals were separated from modern humans in both the principal components and canonical variates analyses. They were much further in Mahalanobis dis- tances from all modern human populations than any two modern human groups were from each other. Most of the previously described temporal bone traits contributed to this separation. Am J Phys Anthropol 120:323-338, 2003. © 2003 Wiley-Liss, Inc.

The Neanderthal taxonomic position is a matter of wide disagreement among paleoanthropologists. Some workers consider this fossil human group to represent a different species, Homo neanderthalensis, while others see it as a subspecies of Homo sapiens. This study developed two models of morphological variation to be applied to a comparison between Neanderthals and modern humans: modern human populations provided a measure of intra-specific variation, while the species and subspecies of Pan provided measures of both intra- and inter-specific morphological differences. Although such an approach has been advocated strongly, it has not been systematically undertaken until recently. The techniques of geometric morphometrics were used to collect data in the form of three-dimensional coordinates of craniofacial landmarks. The data were processed using generalized procrustes analysis, and analyzed by an array of multivariate statistical methods, including principal components analysis, canonical variates analysis and Mahalanobis D 2 . The morphological distances between Neanderthals and modern humans, and between Neanderthals and Late Paleolithic/early anatomically modern specimens, are consistently greater than the distances among recent human populations, and greater than the distances between the two chimpanzee species. Furthermore, no strong morphological similarities were found between Neanderthals and Late Paleolithic Europeans. This study does not find evidence for Neanderthal contribution to the evolution of modern Europeans. Results are consistent with the recognition of Neanderthals as a distinct species. 2003 Elsevier Science Ltd. All rights reserved.

Anatomy and morphometrics have been experiencing a new renaissance in recent decades due to the new techniques and computed methodology used in imaging and statistics. Following this revolution, anatomical systems are currently analyzed by investigating the relationships among their components, in ontogeny and phylogeny. Accordingly, evolution is no more interpreted in terms of single and independent traits, but through integrated patterns and more comprehensive processes. In this sense, paleoneurology should be interpreted as the study of the relationships between brain and braincase during evolution. Morphogenesis is based on the functional and structural relationships between soft and hard tissues. The bones of the braincase, the cerebral cortex, the vascular networks, the connective layers and the cerebrospinal fluid constitute a balanced morphogenetic complex which constrains and influences evolutionary changes. Within this network, the brain largely shapes the bones in the upper endocranial areas, while in the lower endocranial areas the reverse relationship is more likely, due to constraints associated with the facial block and with the cranial base. Most of the spatial changes described in hominid paleoneurology are associated with the fronto-parietal lateral expansion of the endocranial volumes, and modern humans display a further dilation of the whole parietal surface. The study of endocasts can only provide information on size and shape changes associated with the neurocranial morphology, and fields like histology and neuroanatomy are necessary to support robust evolutionary hypotheses. Integration with neuropsychology and other biomedical fields is furthermore necessary to evaluate possible relationships between brain spatial organization and functional topics, such as metabolism or cognition.

Neanderthals and modern humans share a similar cranial capacity but different neurocranial organization. Recently, digital anatomy and computed morphometrics have generated a revolution in functional craniology, allowing quantitative analyses to investigate integration and correlation among the anatomical elements, both in ontogeny and phylogeny. Despite some derived endocranial traits, Neanderthals display a general plesiomorph organization of the braincase. Geometrical and structural constraints between the endocranial soft and hard tissues may have induced morphogenetic limits to the growth and developmental processes. At the same time, heat production associated with a large cranial capacity and a plesiomorph vascular system may have also involved thermal limits. Although in paleontology morphogenetic and metabolic processes can only be investigated through indirect evidence, such hypotheses merit attention when considering the patterns of brain evolution in the genus Homo. It is tempting to wonder whether these limits may be also related to possible factors associated with the extinction of Neanderthals.

Vesalius' short chapter on craniology and the “unnatural” shapes that skulls could take is a uniquely interesting illustration of the young anatomist's position halfway between a traditional belief in a standard or canonical “natural” human anatomy and the host of variations confronted in his day-to-day observation of actual cadavers. His interest in variability is marked in both editions of De humani corporis fabrica (1543, 1555), and it is no coincidence that two of the anatomical features that today bear the great anatomist's name are atypical. In their shape, all of the five skulls that illustrate Chapter 5 of Book I of the Fabrica fall within margins of variability recognized as standard today, but even in Vesalius' own century it was noticed that the sutures in the four “unnatural” skulls do not occur in real life. The article considers the meaning of this unusual departure from his reliance upon observation and includes a translation of Vesalius' craniology chapter from the original Latin, with annotations and two appendices containing his 1555 revisions and clinical addenda. Clin. Anat. 13:311–320, 2000. © 2000 Wiley-Liss, Inc.

Midsagittal cerebral morphology provides a homologous geometrical reference for brain shape and cortical vs. subcortical spatial relationships. In this study, midsagittal brain shape variation is investigated in a sample of 102 humans, in order to describe and quantify the major patterns of correlation between morphological features, the effect of size and sex on general anatomy, and the degree of integration between different cortical and subcortical areas. The only evident pattern of covariation was associated with fronto-parietal cortical bulging. The allometric component was weak for the cortical profile, but more robust for the posterior subcortical areas. Apparent sex differences were evidenced in size but not in brain shape. Cortical and subcortical elements displayed scarcely integrated changes, suggesting a modular separation between these two areas. However, a certain correlation was found between posterior subcortical and parietal cortical variations. These results should be directly integrated with information ranging from functional craniology to wiring organization, and with hypotheses linking brain shape and the mechanical properties of neurons during morphogenesis.

Understanding the mechanical features of cortical bone and their changes with growth and adaptation to function plays an important role in our ability to interpret the morphology and evolution of craniofacial skeletons. We assessed the elastic properties of cortical bone of juvenile and adult baboon mandibles using ultrasonic techniques. Results showed that, overall, cortical bone from baboon mandibles could be modeled as an orthotropic elastic solid. There were significant differences in the directions of maximum stiffness, thickness, density, and elastic stiffness among different functional areas, indicating regional adaptations. After maturity, the cortical bone becomes thicker, denser, and stiffer, but less anisotropic. There were differences in elastic properties of the corpus and ramus between male and female mandibles which are not observed in human mandibles. There were correlations between cortical thicknesses and densities, between bone elastic properties and microstructural configuration, and between the directions of maximum stiffness and bone anatomical axes in some areas. The relationships between bone extrinsic and intrinsic properties bring us insights into the integration of form and function in craniofacial skeletons and suggest that we need to consider both macroscopic form, microstructural variation, and the material properties of bone matrix when studying the functional properties and adaptive nature of the craniofacial skeleton in primates. The differences between baboon and human mandibles is at variance to the pattern of differences in crania, suggesting differences in bone adaption to varying skeletal geometries and loading regimes at both phylogenetic and ontogenetic levels.

Torus mandibularis is a rounded bony protuberance on the lingual surface of the mandible and usually found above the myolohyoid line, medial to the molar roots. This report describes the frequency and morphology of torus and also proffers the likely cause among black South Africans. A total of 284 modern skeletal specimens were obtained from the Raymond Dart Collection of Human Skeletons at the School of Anatomical Sciences, University of the Witwatersrand. The mandibles were classified into dentate and edentulous, while those with torus, especially in dentate mandibles, were reviewed for side location, type and shape. No measurements were made, consistent with the view that these characteristics are non-metrical and should be assessed by means of a standard observatory procedure. Out of 246 dentate mandibles, 60 (24.4%) were found to have torus and only 1 (4.3%) out of the 23 male edentulous mandibles; the difference is statistically significant (P=2.8%). The torus distribution among males and females was 48 (80%) and 12 (20%), respectively, and again statistically significant (P< 0.05). Prevalence of torus was highest in the 40-60 years age group. The morphology of the torus showed that 37 (61.7%) were bilateral in location, 42 (70%) were of the solitary type and 31 (51.7%) were round in shape. The formation of torus follows the threshold model which holds that this is primarily a genetic trait, but with environmental factors such as mechanical stress necessary for its development.

An evolutionary, diachronic approach to the phenotypic craniofacial pattern arisen in a human population after high levels of admixture and gene flow was achieved by means of geometric morphometrics. Admixture has long been studied after molecular data. Nevertheless, few efforts have been made to explain the morphological outcome in human craniofacial samples. The Spanish-Amerindian contact can be considered a good scenario for such an analysis. Here we present a comparative analysis of craniofacial shape changes observed between two putative ancestor groups, Spanish and precontact Aztecs, and two diachronic admixed groups, corresponding to early and late colonial periods from the Mexico's Central Valley. Quantitative shape comparisons of Amerindian, Spanish, and admixed groups were used to test the expectations of quantitative genetics for admixture events. In its simplest form, this prediction states that an admixed group will present phenotypic values falling between those of both parental groups. Results show that, in general terms, although the human skull is a complex, integrated structure, the craniofacial morphology observed fits the theoretical expectations of quantitative genetics. Thus, it is predictive of population structure and history. In fact, results obtained after the craniofacial analysis are in accordance with previous molecular and historical interpretations, providing evidence that admixture is a main microevolutionary agent influencing modern Mexican gene pool. However, expectations are not straightforward when moderate shape changes are considered. Deviations detected at localized structures, such as the upper and lower face, highlight the evolution of a craniofacial pattern exclusively inherent to the admixed groups, indicating that quantitative characters might respond to admixture in a complicated, nondirectional way.

This study reports a comparison of molar crown and cusp size and shape in the Swartkrans early Homo mandible SK 15 with relevant Plio-Pleistocene taxa. Univariate and multivariate methods are employed to consider the morphological affinities of this specimen and to assess its taxonomy. The case exists for classifying SK 15 in Homo habilis with 11 features aligning it with this species. The results of multivariate studies are consistent with this hypothesis. Moreover, SK 15 lacks a number of important features that characterise the mandibular molars of Homo sapiens erectus. Considerable evidence for parallelism in the dental morphology of SK 15 and H. habilis with A. robustus is discussed. Fossil evidence for the presence of H. sapiens erectus during the Plio-Pleistocene of South Africa presently seems to be lacking. Archaeological interpretations should take greater account of this gap in the fossil record.

Reports in the literature suggest that diagnostic differences in craniofacial morphology between blacks and whites arise very early in development. These reports, however, have not been consistent regarding which traits are diagnostic and have failed to provide forensic anthropologists with a reliable method of assessment. In an effort to clarify the situation, 13 non-metric craniofacial traits were scored and analyzed statistically in a sample of 70 black and white perinatal specimens obtained from the Smithsonian’s fetal osteology collection. Chi-square analysis revealed significant ( p < 0.05) differences in the distribution of five of the 13 nonmetric traits examined. Compared with black perinates, white perinates more frequently possessed a relatively narrow supraoccipital portion of the occipital bone, a prominent anterior nasal spine, ‘‘deep’’subnasal margins, an elongated vomer, and semi-circular temporal squamae. When these five traits were entered into a stepwise logistic regression, temporal squamous shape, vomer shape and subnasal margin definition were found to be predictive of race (79.1% overall correct classification). An independent sample of 39 black and white perinates was then used to validate the results; overall, 67.5% of the validation sample could be classified correctly. Reasons for the disparity in correct classification rates between the initial and follow-up sample are provided. Results of the present study may be useful for anthropologists who encounter unidentified cranial material from this age range. # 2005 Elsevier Ireland Ltd. All rights reserved.

Recent discovery of crania, dentitions, and postcrania of a primitive anthropoidean primate, Proteopithecus sylviae , at the late Eocene L-4l quarry in the Fayum, Egypt, provides evidence of a new taxonomic family of early African higher primates, the Proteopithecidae. This family could be part of the basal radiation that produced the New World platyrrhine primates, or it could be unrelated to any subsequent lineages. Although no larger than a small callitrichid or a dwarf lemur, this tiny primate already possessed many of the derived features of later anthropoids and was a diurnal and probably dimorphic species. In dental formula and other dental proportions, as well as in known postcranial features, Proteopithecus more nearly resembles platyrrhines than does any other Old World higher primate. The small size of the Proteopithecus cranium demonstrates that the defining cranial characteristics of Anthropoidea did not arise as a consequence of an increase in size during derivation from earlier prosimians.

Previous studies of genetic markers and mitochondrial DNA have found that the amount of variation among major geographic groupings of Homo sapiens is relatively low, accounting for roughly 10% of total variation. This conclusion has had implications for the study of human variation and consideration of alternative models for the origin of modern humans. By contrast, it has often been assumed that the level of among-group variation for morphological traits is much higher. This study examines the level of among-group variation based on Craniometric data from a large sample of modern humans originally collected by W. W. Howells. A multivariate method based on quantitative genetics theory was used to provide an estimate of FST — a measure of among-group variation that can be compared with results from studies of genetic markers. Data for 57 Craniometric variables on 1,734 crania were analyzed. These data represent six core areas: Europe, Sub-Saharan Africa, Australasia, Polynesia, the Americas, and the Far East. An additional set of analyses was performed using a three-region subset (Europe, Sub-Saharan Africa, and the Far East) to provide comparability with several genetic studies. The minimum FST (assuming complete heritability) for the three-region analysis is 0.065, and the minimum FST for the six-region analysis is 0.085. Both of these are less than the average FST from genetic studies (average estimates of 0.10–0.11). The smaller value of the minimum FST estimates is expected since it provides an estimate of FST expected under complete heritability. Using an estimate of average craniometric heritability from the literature provides an estimate of FST of 0.112 for the three-region analysis and 0.144 for the six-region analysis. These results show that genetic and craniometric data are in agreement, qualitatively and quantitatively, and that there is limited variation in modern humans among major geographic regions. © 1994 Wiley-Liss, Inc.

The "out-of-Africa" models for origins of modern Homo sapiens incorporate Skhul as one site documenting that early origination. However, only Skhul V is usually considered in the comparative craniology of the question, neglecting the other substantial crania, Skhul IV and IX. Craniometric comparison demonstrates that IV and IX amplify the picture of continuous gradations of Neandertal-to-modern variations throughout the Levant; much variation is thus represented within this one site, raising serious questions about Neandertals and moderns being discrete and long-separated species. Qafzeh 6 too is craniophenetically closer to Neandertals than to the true anatomically modern people of the European Upper Paleolithic. Proper distance analysis of Border Cave 1 cranium shows it is actually far removed from modern African populations. References to Qafzeh, Skhul, and Border Cave as "fully anatomically modern" require reconsideration.

This paper is the second of a series on the craniology of four species of Bos . It is a further study of the skulls of British domestic cattle which are used in an attempt to establish a basic craniology for the genus. Part 1 ( Grigson, 1974 ) dealt with nomenclature, material, history, age assessment and absolute size. This paper deals first with cranial proportions and then with cranial angles. The results show that the proportions of the skull depend on its size and, to a lesser extent, on its sex, cows having relatively narrow skulls, with short horncores, but sometimes longer horns than bulls. Cranial angles seem to be independent of size or sex, but are influenced slightly by age, and also, in some cases, strongly by breed.

Since its initiation in 1966 the Omo Research Expedition has recovered a series of hominid fossils, in association with many vertebrate taxa, from formations of Pliocene/Pleistocene age from the lower Omo basin, southern Ethiopia. These fossiliferous formations span a time range from over 4.2 m.y. to about 1.4 m. y. on the basis of K/A age determination. Hominid remains have been found so far to occur at two localities in the upper part of the Usno Formation (∼ 2.9 m.y.) and in the Shungura Formation at 79 localities from successive Members B through levels postdating J, a time span between 3 m.y. and 1.4 m.y. The remains—inventoried here according to skeletal part, locality and stratigraphic level, age and situation—include numerous isolated and associated teeth, mandibles, partial maxillae, portions of crania, and elements of the postcranial skeleton.

Contusus Whitley, 1947 is considered a valid generic name for two species from temperate shallows of Australia and New Zealand, and is redefined. The genus differs significantly in dorsal craniology from the related genera Amblyrhynchotes, Fugu, and Torquigener, particularly in the shape of frontals and prefrontals and in having contact between the sphenotic and supraoccipital. C. richei (Freminville) is redesoribed, and C. brevicaudus n.sp. is described for the first time. Full synonymies are provided for both species. Generic and specific keys are given.

The present study concerns with the methodological aspects of the vestibular method of orientating the cranium, which is mainly recommended for its physiological significance. Three dimensional coordinates of 36 landmarks were examined in the vestibular coordinate system which is defined by the plane of the lateral semicircular canals. This was determined utilizing a tomography apparatus. The coordinate data were obtained from 63 macerated modern Japanese crania by recording the landmarks with the cubic craniophore and then translocating the landmarks into the vestibular coordinate system.Measurement errors were found to be small and variance as represented by bilateral asymmetry in the orientation of the lateral semicircular canals were estimated to be insignificant to the total variance. Thus, no apparent evidence exists indicating an instability of the vestibular orientation. Variability of the landmarks was investigated in the vestibular, Frankfort horizontal and glabella-inion line coordinate systems. This comparison revealed that the vestibular coordinate system characteristically shows a relasively high variability strongest in the facial landmarks.

This paper is the third in a series on the craniology of four species of Bos and it is the last of the three papers in which the skulls of British domestic cattle are used in an attempt to establish a basic craniology for the genus. Part 1 ( Grigson, 1974 ) dealt with nomenclature, material, history, age assessment and absolute size. Part 2 ( Grigson, 1975 ) dealt with cranial proportions and angles. This paper deals first with sagittal profiles and then with other non-measurable characters. Sagittal profiles may be rounded or pointed with some intermediate forms. The rounded shape (an infantile character) persists throughout life in some breeds and is unaffected by age, sex or size. The pointed form develops with age in some breeds and is probably more marked in older and larger animals. Seventeen other minor characters are examined for the effects of age, sex, breed and size.

The first three papers in this series ( Grigson, 1974 , Grigson, 1975 , Grigson, 1976 ) studied the basic craniology of the genus Bos using B. taurus as an example; the fourth paper ( Grigson 1978 ) concluded that B. primigenius and B. taurus form a continuum. The present paper examines absolute size, proportional relationships, sagittal profiles, cranial angles and non-measurable characters of B. indicus, and notes similarities to and differences from B. taurus and B. primigenius. It suggests that B. indicus may be more closely related to B. namadicus, but evidence for this will be more fully discussed in the last paper of the series (Grigson, in prep.). The occurrence of neotenic characters in B. indicus is discussed.

Functionally significant aspects of skull morphology were examined in Eocene miacids and in early members of the modern carnivore families to see if functional craniology might shed light on factors involved in the origin and early evolution of the modern carnivores. No key innovations are apparent at the beginning of the modern carnivore radiation, and an alternative hypothesis to account for that radiation is proposed: the radiation represents the filling of niches vacated by the extinction of several groups of archaic carnivores in the late Eocene. Differences that distinguish modern viverrids, canids, felids, and mustelids from each other today were less pronounced in the Oligocene, when these families first appeared, and provide no insights into possible ecological differences at the family level. However, body size differences among the early members of the modern carnivore families suggest that partitioning of prey resources by size may have been a factor in their initial radiation. Comparison of cranial morphology in Eocene miacids, early members of the modern carnivore families, and living carnivores allows reconstruction of the primitive conditions of carnivore skull morphology and determination of the pathways of morphological transformation that resulted in the diversity of skull morphology seen in modern carnivores.

This paper is the first of a series on the craniology of four species of Bos . Here (and in the next paper) Bos taurus in Britain is used to establish a basic craniology for the genus. In the initial sections notes are made on the nomenclature, material available, history, and age assessment of B. taurus . The subsequent section deals with the effects of sex, age and breed on absolute size. The results show that Bos taurus is very variable, particularly in the length of the horncore. Sex influences certain dimensions very greatly, particularly those of breadth. Although the horns of cows are often longer than those of bulls of the same breed the horn cores may be shorter in cows. In studying the effects of age it can be seen that growth rates are initially very high, slowing down at about three years of age. Tooth row length decreases with age and hence it is a particularly unreliable indicator of size. Obviously breed affects size and it has been possible to divide the skulls studied into size groups which correspond well with known body weights.