On the squamosal suture of KNM-WT 17000.

The extensive overlap of the temporal squama on the parietal in KNM-WT 17000 is restricted to a narrow segment of the arc of the squamosal suture. It appears as a long, narrow, posterosuperior extension onto the calvarial wall. The long axis of this extended strip is aligned with what appears to be the most hypertrophied section of the temporalis muscle fan. The substantial differences between the squamosal suture and associated masticatory elements of KNM-WT 17000 and those of Australopithecus boisei provide an opportunity to evaluate the various forces molding the anatomy of the squamosal suture of A. boisei. It is suggested that the extreme flare of the zygomatic arches in the latter accounts for these differences.     

Stature-at-death of KNM-WT 15000

The specimen KNM-WT 15000 is an exceptionally complete 1.53 Myr juvenile skeleton of Homo erectus from West Turkana, Kenya. It therefore provides a unique opportunity to examine stature estimates of fossil hominids based strictly on long bone lengths. Using recovered axial and appendicular elements of KNM-WT 15000 that contributed to stature during life, we conclude that KNM-WT 15000 was much shorter at time-of-death than previous estimates that used only appendicular elements. We conservatively estimate stature-at-death at about 147 cm, although this individual could have been as short as 141 cm. Because long bone based estimates of stature also imply the axial skeletal proportion, our new stature estimate stems from the recognition of axial/appendicular disproportion in the individual KNM-WT 15000. It is possible that the peripubescent age-at-death of this specimen, and any resulting differential maturity between the appendicular and axial skeleton, may have contributed to previous overestimates of stature-at-death. However, the possibility that this individual was abnormal, as implied by axial/appendicular disproportion, remains to be fully tested. Regardless, these results suggest that some interpretations of the biology of early African Homo erectus, largely based upon KNM-WT 15000, should be viewed with caution. 5 Primate Evolution and Morphology Group, Department of Human     

Skeletal age, dental age, and the maturation of KNM-WT 15000

The skeleton of the Homo erectus boy from West Lake Turkana, Kenya (KNM-WT 15000), is remarkably complete, and this individual has thus provided a case study for several researchers examining Homo erectus growth. Using data from a longitudinal study of Montreal French-Canadian children, it is shown that while dental and skeletal ages match reasonably well at the level of a sample of children, individuals can display differences between skeletal and dental ages of 2 years or more. Furthermore, the relationship between these two markers may change over time in individual children. It is also possible to find children with patterns of dental maturation similar to KNM-WT 15000's pattern in the Montreal sample. Therefore, neither the discrepancy between skeletal age and dental age alone nor the pattern of dental maturation as assessed by dental stages precludes a human-like pattern of growth, including an adolescent growth spurt, for this individual. Some indicators (e.g., estimated body size for predicted age, and enamel formation) do suggest possible growth-patterning differences from modern humans, and therefore earlier maturation is a reasonable hypothesis, but caution is warranted, given the large degree of modern human variation in developmental markers and the inherent uncertainty in precise estimation of KNM-WT 15000's maturational parameters.     

Evolutionary integration of the frog cranium

Evolutionary integration (covariation) of traits has long fascinated biologists because of its potential to elucidate factors that have shaped morphological evolution. Studies of tetrapod crania have identified patterns of evolutionary integration that reflect functional or developmental interactions among traits, but no studies to date have sampled widely across the species-rich lissamphibian order Anura (frogs). Frogs exhibit a vast range of cranial morphologies, life history strategies, and ecologies. Here, using high-density morphometrics we capture cranial morphology for 172 anuran species, sampling every extant family. We quantify the pattern of evolutionary modularity in the frog skull and compare patterns in taxa with different life history modes. Evolutionary changes across the anuran cranium are highly modular, with a well-integrated “suspensorium” involved in feeding. This pattern is strikingly similar to that identified for caecilian and salamander crania, suggesting replication of patterns of evolutionary integration across Lissamphibia. Surprisingly, possession of a feeding larval stage has no notable influence on cranial integration across frogs. However, late-ossifying bones exhibit higher integration than early-ossifying bones. Finally, anuran cranial modules show diverse morphological disparities, supporting the hypothesis that modular variation allows mosaic evolution of the cranium, but we find no consistent relationship between degree of within-module integration and disparity.     

Hominin diversity in the Middle Pliocene of eastern Africa: the maxilla of KNM-WT 40000

The 3.5-Myr-old hominin cranium KNM-WT 40000 from Lomekwi, west of Lake Turkana, has been assigned to a new hominin genus and species, Kenyanthropus platyops, on the basis of a unique combination of derived facial and primitive neurocranial features. Central to the diagnosis of K. platyops is the morphology of the maxilla, characterized by a flat and relatively orthognathic subnasal region, anteriorly placed zygomatic processes and small molars. To study this morphology in more detail, we compare the maxillae of African Plio-Pleistocene hominin fossils and samples of modern humans, chimpanzees and gorillas, using conventional and geometric morphometric methods. Computed tomography scans and detailed preparation of the KNM-WT 40000 maxilla enable comprehensive assessment of post-mortem changes, so that landmark data characterizing the morphology can be corrected for distortion. Based on a substantially larger comparative sample than previously available, the results of statistical analyses show that KNM-WT 40000 is indeed significantly different from and falls outside the known range of variation of species of Australopithecus and Paranthropus, contemporary Australopithecus afarensis in particular. These results support the attribution of KNM-WT 40000 to a separate species and the notion that hominin taxonomic diversity in Africa extends back well into the Middle Pliocene.     

Affinities of the Swartkrans 847 hominid cranium

Further evidence of the presence of a second hominid species at the Swartkrans locality was obtained in 1969 when the SK.847 specimen was discovered by us to represent the same individual as the SK.80 maxilla. The SK.847 specimen had previously been regarded as robust australopithecine, whereas the latter was first attributed to Telanthropus capensis and subsequently to a species of the genus Homo. Recent criticism of our interpretation of these remains has not evaluated and analyzed critically the primary fossil evidence. Instead it relies on a strict adherence to an as yet unsubstantiated hypothesis that posits only a single hominid species at any point in space and time in the Cenozoic history of Hominidae.     

Sexual dimorphism in the growth of the cranium

The major sexual dimorphisms in body size appear at puberty but, by then, 95% of the growth of the cranium is completed. As sexual dimorphism in the cranium is as great as for other parts of the body, this suggests that it must appear at an earlier age, and that cranium/body size ratios for the two sexes will vary during growth. Results from a longitudinal study of Montreal children are used to investigate this phenomenon. The effect is expressed quantitatively by proportional growth and growth velocity curves, based on the final size of boys, which show that the dimorphism indeed makes an early appearance. The data are also analyzed on an age scale relative to the ages of peak growth velocity in stature, derived from the individual growth curves. This shows that although there is a minor pubertal spurt in growth for the external cranial dimensions of boys, it contributes relatively little to the final dimorphism in cranial size. To summarize this aspect of growth, an index of cephalization is calculated: head length × head width/stature. Cross-sectional standards for the change of the mean index with age show a linear decline for boys and girls until puberty, with a constant difference between them. After puberty, the index becomes equal in the two sexes. Individual development curves for the index are however not linear.     

Morphological variations of the cranium within the genusLeontopithecus

Multivariate analysis methods were applied to the cranial measurements ofLeontopithecus. InLeontopithecus chrysomelas, the face is generally narrow and the cranial shape is relatively unique. Especially, the male has extremely narrow face and quite unique cranial shape amongLeontopithecus. Leontopithecus rosalia has the broad face compared with the other species. The cranial size ofL. rosalia is as large as that ofL. chrysomelas. Male ofLeontopithecus chrysopygus is the largest in overall size of the cranium, and has the widest braincase.     

Evidence of pathological conditions in the Florisbad cranium

Palaeopathological studies of the middle Pleistocene cranium from Florisbad (Free State, South Africa) document the presence of extensive cortical lesions and areas of thinning, a widened medullary cavity with destruction of the diploë, orbital roof lesions, a benign ectocranial neoplasm, and evidence for alveolar destruction, resorption, and antemortem tooth loss. Differential diagnosis suggests one or more possible aetiologies, including a haematological disorder, metabolic condition(s), Paget’s disease of bone, or non-specific infection perhaps following trauma. Moreover, if not directly associated with those on the external vault, orbital lesions alone could have been caused by infection or an indeterminable factor such as pressure from an enlarged organ. Multiple parasagittal lesions on the internal vault cortex probably represent expansile lesions left by enlarged arachnoid granulations. A multifactorial model of pathogenesis may be most appropriate to account for dentoalveolar lesions and antemortem tooth loss. Additionally, there are clear indications of diagenetic alteration deep within the vault, as well as multiple signs of degeneration on the cranium. These complicate the assessment of pathological alterations and identification of their possible aetiology. The Florisbad cranium is the latest specimen to join the growing sample of Pleistocene hominin remains with non-fatal and non-trivial pathological disorders adding to understanding of early human ecology and lifestyle.     

Biomechanical properties of human cranium: Age-relayed aspects

Biomechanical properties of the human skull affect its dynamic tensility (pliability or compliance) at changes of intracranial volume and pressure (ΔV/ΔP). The work substantiates a possibility of noninvasive and dynamic evaluation of cranial compliance by synchronous recording of transcranial dopplerogram of middle cerebral artery and cranial bioimpedance that provides information about pulsative changes of intracranial pressure and volume, respectively, with subsequent computer pattern and phasic analysis of these processes. The characteristic peculiarities of the cranial compliance at rest and during action of functional hemo- and liquorodynamic tests were traced in people of the middle (40–50 years) and elderly (70–85 years) age groups as compared with the young group (20–30 years). A relative decrease of this parameter has been revealed in the middle age group due to an increase of rigidity of skull bones and ligaments, which indicates a decrease of tolerance of the intracranial circulatory system. However, in the group of 70–85 years the compliance parameters rose due to an increase of intracranial liquor volume and activation of liquor circulation inside the craniospinal space, which is a compensatory mechanism for maintenance of the adequate brain circulatory-metabolic activity.     

Geographical variations in the cranium ofSaguinus geoffroyi

In terms of craniometry, we examinedHershkovitz's hypotheses that, inSaguinus geoffroyi, populations on the western shore of the Rio Atrato were closely related toS. leucopus, and that a morphocline could be traced from the easternS. geoffroyi population to the western one. We detected a morphological sequence from east to west (or east to west) but did not find any evidence supporting the former hypothesis.