The energy costs of wading in water.

Studies measuring the energy costs of wading in water have been limited to higher walking speeds in straight lines, in deep water. However, much foraging in water, by both humans and other primates, is conducted in the shallows and at low speeds of locomotion that include elements of turning, as befits searching for cryptic or hidden foods within a patch. The present study brings together data on the rate of oxygen consumption during wading by humans from previous studies, and augments these with new data for wading in shallower depths, with slower and more tortuous walking, to obtain a better understanding both of the absolute costs of wading in typical scenarios of aquatic foraging and of how the cost of wading varies as a function of water depth and speed of locomotion. Previous and present data indicate that, at low speeds, wading has a similar energetic cost to walking on land, particularly at lower water depths, and only at higher speeds is the cost of wading noticeably more expensive than when water is absent. This is probably explained by the relatively small volume of water that must be displaced during locomotion in shallow waters coupled with the compensating support to the limbs that the water affords. The support to the limbs/body provided by water is discussed further, in the context of bipedal locomotion by non-human primates during wading.

Estimation of sex from cranial measurements in a Western Australian population.

It is widely accepted that the most accurate statistical estimations of biological attributes in the human skeleton (e.g., sex, age and stature) are produced using population-specific standards. As we previously demonstrated that the application of foreign standards to Western Australian individuals results in an unacceptably large sex bias (females frequently misclassified), the need for population-specific standards is duly required and greatly overdue. We report here on the first morphometric cranial sexing standards formulated specifically for application in, and based on the statistical analysis of, contemporary Western Australian individuals. The primary aim is to investigate the nature of cranial sexual dimorphism in this population and outline a series of statistically robust standards suitable for estimating sex in the complete bone and/or associated diagnostic fragments. The sample analysed comprised multi-detector computed tomography cranial scans of 400 individuals equally distributed by sex. Following 3D volume rendering, 31 landmarks were acquired using OsiriX, from which a total of 18 linear inter-landmark measurements were calculated. Measurements were analysed using basic descriptive statistics and discriminant function analyses employing jackknife validations of classification results. All measurements (except frontal breadth and orbital height - Bonferroni corrected) are sexually dimorphic with sex differences explaining 3.5-48.9% of sample variance. Bizygomatic breadth and maximum length of the cranium and the cranial base contribute most significantly to sex discrimination; the maximum classification accuracy was 90%, with a -2.1% sex-bias. We conclude that the cranium is both highly dimorphic and a reliable bone for estimating sex in Western Australian individuals.

Concordance of traditional osteometric and volume-rendered MSCT interlandmark cranial measurements.

The statistical quantification of error and uncertainty is inherently intertwined with ascertaining the admissibility of forensic evidence in a court of law. In the forensic anthropological discipline, the robustness of any given standard should not only be evaluated according to its stated error but by the accuracy and precision of the raw data (measurements) from which they are derived. In the absence of Australian contemporary documented skeletal collections, medical scans (e.g. multislice computed tomography-MSCT) offer a source of contemporary population-specific data for the formulation of skeletal standards. As the acquisition of morphometric data from clinical MSCT scans is still relatively novel, the purpose of this study is to assess validity of the raw data that is being used to formulate Australian forensic standards. Six human crania were subjected to clinical MSCT at a slice thickness of 0.9 mm. Each cranium and its corresponding volume-rendered three-dimensional MSCT image were measured multiple times. Whether differences between MSCT and dry bone interlandmark measurements are negligible is statistically quantified; intra- and inter-observer measurement error is also assessed. We found that traditional bone measurements are more precise than their MSCT counterparts, although overall differences between the two data acquisition methods are negligible compared to sample variance. Cranial variation accounted on average for more than 20× the variance explained by MSCT vs. bone measurements. Similarly, although differences between operators were sometimes significant compared to intra-operator variance, they were negligible when compared to sample variance, which was on average 12× larger than that due to inter-operator differences.

The application of traditional and geometric morphometric analyses for forensic quantification of sexual dimorphism: preliminary investigations in a Western Australian population.

A current limitation of forensic practice in Western Australia is a lack of contemporary population-specific standards for biological profiling; this directly relates to the unavailability of documented human skeletal collections. With rapidly advancing technology, however, it is now possible to acquire accurate skeletal measurements from 3D scans contained in medical databases. The purpose of the present study, therefore, is to explore the accuracy of using cranial form to predict sex in adult Australians. Both traditional and geometric morphometric methods are applied to data derived from 3D landmarks acquired in CT-reconstructed crania. The sample comprises multi-detector computed tomography scans of 200 adult individuals; following 3D volume rendering, 46 anatomical landmarks are acquired using OsiriX (version 3.9). Centroid size and shape (first 20 PCs of the Procrustes coordinates) and the inter-landmark (ILD) distances between all possible pairs of landmarks are then calculated. Sex classification effectiveness of the 3D multivariate descriptors of size and shape and selected ILD measurements are assessed and compared; robustness of findings is explored using resampling statistics. Cranial shape and size and the ILD measurements are sexually dimorphic and explain 3.2 to 54.3 % of sample variance; sex classification accuracy is 83.5-88.0 %. Sex estimation using 3D shape appears to have some advantages compared to approaches using size measurements. We have, however, identified a simple and biologically meaningful single non-traditional linear measurement (glabella-zygion) that classifies Western Australian individuals according to sex with a high degree of expected accuracy (87.5-88 %).

Estimation of sex from sternal measurements in a Western Australian population.

In Australia, particularly Western Australia, there is a relative paucity of contemporary population-specific morphometric standards for the estimation of sex from unknown skeletal remains. This is largely a historical artefact from lacking, or poorly documented, repositories of human skeletons available for study. However, medical scans, e.g. MSCT (multislice spiral computed tomography) are an ingenious and practical alternative source for contemporary data. To that end, this study is a comprehensive analysis of sternal sexual dimorphism in a sample of modern Western Australian (WA) individuals with a main purpose to develop a series of statistically robust standards for the estimation of sex. The sample comprises thoracic MSCT scans, with a mean of 0.9 millimeter (mm) slice thickness, on 187 non-pathological sterna. Following 3D volume rendering, 10 anatomical landmarks were acquired using OsiriX(®) (version 3.9) and a total of 8 inter landmark linear measurements were calculated using Morph Db (an in-house developed database application). Measurements were analyzed using basic descriptive statistics and discriminant function analyses, with statistical analyses performed using SPSS 19.0. All measurements are sexually dimorphic and sex differences explain 9.8-47.4% of sample variance. The combined length of the manubrium and body, sternal body length, manubrium width, and corpus sterni width at first sternebra contribute significantly to sex discrimination and yield the smallest sex-biases. Cross-validated classification accuracies, i.e., univariate, stepwise and direct function, are 72.2-84.5%, with a sex bias of less than 5%. We conclude that the sternum is a reliable element for sex estimation among Western Australians.

The relative cost of bent-hip bent-knee walking is reduced in water.

The debate about how early hominids walked may be characterised as two competing hypotheses: They moved with a fully upright (FU) gait, like modern humans, or with a bent-hip, bent-knee (BK) gait, like apes. Both have assumed that this bipedalism was almost exclusively on land, in trees or a combination of the two. Recent findings favoured the FU hypothesis by showing that the BK gait is 50-60% more energetically costly than a FU human gait on land. We confirm these findings but show that in water this cost differential is markedly reduced, especially in deeper water, at slower speeds and with greater knee flexion. These data suggest that the controversy about australopithecine locomotion may be eased if it is assumed that wading was a component of their locomotor repertoire and supports the idea that shallow water might have been an environment favourable to the evolution of early forms of "non-optimal" hominid bipedalism.

Wading for food the driving force of the evolution of bipedalism?

Evidence is accumulating that suggests that the large human brain is most likely to have evolved in littoral and estuarine habitats rich in naturally occurring essential fatty acids. This paper adds further weight to this view, suggesting that another key human trait, our bipedality might also be best explained as an adaptation to a water-side niche. Evidence is provided here that extant apes, although preferring to keep dry, go into water when driven to do so by hunger. The anecdotal evidence has suggested that they tend to do this bipedally. Here, a new empirical study of captive bonobos found them to exhibit 2% or less bipedality on the ground or in trees but over 90% when wading in water to collect food. The skeletal morphology of AL 288-1 ("Lucy") is shown to indicate a strong ability to abduct and adduct the femur. These traits, together with a remarkably platypelloid pelvis, have not yet been adequately explained by terrestrial or arboreal models for early bipedalism but are consistent with those expected in an ape that adopted a specialist side-to-side 'ice-skating' or sideways wading mode. It is argued that this explanation of A. afarensis locomotor morphology is more parsimonious than others which have plainly failed to produce a consensus. Microwear evidence of Australopithecus dentition is also presented as evidence that the drive for such a wading form of locomotion might well have been waterside foods. This model obtains further support from the paleo-habitats of the earliest known bipeds, which are consistent with the hypothesis that wading contributed to the adaptive pressure towards bipedality.