Erectus Specimens Research Articles

Java Man and the Politics of Natural History

Abstract Natural history museums have long escaped postcolonial or decolonial scrutiny; their specimens were and are usually presented as part of the natural world, containing only biological or geological information. However, their collections, like those of other museums, are rooted in colonial practices and thinking. In this article, we sketch a political and decolonial biography of ‘Java Man’, the fossilized remains of a Homo erectus specimen, housed in Naturalis, the Natural History Museum, in the Netherlands. We describe the context of Dutch colonialism and the role of indigenous knowledge and activity in the discovery of Java Man. We also follow Java Man to the Netherlands, where it became a contested specimen and part of a discussion about repatriation. This article argues that the fossils of Java Man and their meanings are products of ‘creolized’ knowledge systems produced by Empire and sites of competing national and disciplinary histories and identities.

An assessment of the late Middle Pleistocene occipital from Apidima 1 skull (Greece)

Recent papers have sparked an ongoing debate on the taxonomic adscription of the late Middle Pleistocene fossil skulls from Apidima (Greece). There is general agreement that the more complete skull Apidima 2 is a member of the Neandertal lineage. However, the evolutionary significance of the anatomy of Apidima 1 is unclear. While de Lumley et al. (2019; CNRS Editions) saw both skulls as belonging to the same deme, Harvati et al. (2019; Nature 571:500) argued that Apidima 1 is the earliest evidence of Homo sapiens in Eurasia. In order to assess the morphological affinities of this fossil skull, we performed both qualitative analyses and a 3D geometric morphometric (3D GM) analysis of twelve 3D landmarks (Asterion, Lambda, Inion) and a curve of semilandmarks along the upper occipital squama of Apidima 1 with a comparative sample of Homo. At the external side of its occipital bone we found some but not all the morphological features classically recognized as Neandertal derived, e.g. a smooth suprainiac fossa and a weak bilaterally protruding transverse occipital torus. Geometric morphometric analyses reveal that Apidima 1 appears in the morphospace close to primitive H. erectus specimens, whose plesiomorphic configuration of the Apidima 1 is mostly expressed in its low and wide occipital; a condition, nonetheless, also found in other Neandertals. All together, we do not find support for the hypothesis that Apidima 1 is the earliest evidence of Homo sapiens in Europe. The presence of Neandertal apomorphic qualitative features together with the existence of primitive occipital among H. neanderthalensis populations points to a Neanderthal adscription for Apidima 1. We believe Apidima 1 may be a brachycephalic female variant of the Neandertal genetic pool. If this interpretation is correct, Neandertal lineage may encompass more anatomical variation than yet realized.

Reevaluation of the body mass estimate for the KNM-ER 5428 Homo erectus talus.

In this study, we reexamined the body mass estimate for the Homo erectus specimen KNM-ER 5428 based on talus dimensions. Previous estimates of >90 kg for this fossil are large in comparison to body mass estimates for other H. erectus specimens. The study sample consisted of tali and femora of 132 modern cadaver males from a documented body mass skeletal collection. We recorded the talus trochlear mediolateral (TTML) breadth and femoral head diameter (FHD) for each modern human specimen, and obtained KNM-ER 5428's TTML values from the literature. We developed regression formulae based on TTML using the body mass estimated from FHD for the entire human sample and for known body masses from a normal-BMI subsample, and then used these formulae to calculate body mass for KNM-ER 5428. In addition, we examined the range of body masses for individuals with TTML measurements comparable to KNM-ER 5428. The body masses of normal-BMI individuals with a TTML ≥32.3 mm (the smaller of the two fossil measurements from the literature) ranged between 60.3 and 86.2 kg and averaged 72.3 kg. The body masses of normal-BMI individuals with a TTML ≥33.7 mm (the larger measurement) ranged between 63.5 and 86.2 kg with a mean of 73.6 kg. The correlations between TTML and body mass are moderate. Revised body mass point estimates for KNM-ER 5428 ranged between 69.2 and 81.6 kg based on TTML, and average 70.5 and 76.0 kg. Results suggest previously published body mass estimates of KNM-ER 5428's are too large. Its body mass was likely between 70 and 76 kg rather than >90 kg.

The effect of ontogeny on estimates of KNM-WT 15000's adult body size

The Homo erectus specimen KNM-WT 15000 has played a critical role in our understanding of body size evolution. New interpretations suggest that KNM-WT 15000 had a younger age-at-death and a more rapid ontogenetic trajectory than previously suggested. Recent fossil discoveries and new interpretations suggest a wide range of body size and shape variation in H. erectus. Based on these new insights, we argue that KNM-WT 15000's adult stature and body mass could have been much smaller than has been traditionally presented in the literature. Using chimpanzee and modern human growth trajectories, we bracketed the range of possibilities for KNM-WT 15000's adult body size between 160.0 and 177.7 cm (5′3″–5′10″) for stature and 60.0 and 82.7 kg (132–182 lbs.) for body mass. These estimates put KNM-WT 15000 near the mean rather than among the largest known H. erectus specimens.

Body size, brain size, and sexual dimorphism in Homo naledi from the Dinaledi Chamber

Homo erectus and later humans have enlarged body sizes, reduced sexual dimorphism, elongated lower limbs, and increased encephalization compared to Australopithecus, together suggesting a distinct ecological pattern. The mosaic expression of such features in early Homo, including Homo habilis, Homo rudolfensis, and some early H. erectus, suggests that these traits do not constitute an integrated package. We examined the evidence for body mass, stature, limb proportions, body size and dental size dimorphism, and absolute and relative brain size in Homo naledi as represented in the Dinaledi Chamber sample. H. naledi stature and body mass are low compared to reported values for H. erectus, with the exception of some of the smaller bodied Dmanisi H. erectus specimens, and overlap with larger Australopithecus and early Homo estimates. H. naledi endocranial volumes (465–560 cc) and estimates of encephalization quotient are also similar to Australopithecus and low compared to all Homo specimens, with the exception of Homo floresiensis (LB1) and the smallest Dmanisi H. erectus specimen (D4500). Unlike Australopithecus, but similar to derived members of genus Homo, the Dinaledi assemblage of H. naledi exhibits both low levels of body mass and dental size variation, with an estimated body mass index of sexual dimorphism less than 20%, and appears to have an elongated lower limb. Thus, the H. naledi bauplan combines features not typically seen in Homo species (e.g., small brains and bodies) with those characteristic of H. erectus and more recent Homo species (e.g., reduced mass dimorphism, elongated lower limb).

Caracterización de las poblaciones de caballitos de mar en diferentes zonas de la costa norte de las regiones occidental y central de Cuba

Los caballitos de mar son peces ornamentales de gran interés para las exhibiciones en el Acuario Nacional de Cuba, por lo que se propuso valorar el estado actual de las poblaciones naturales de las especies Hippocampus reidi (Ginsburg, 1933) e Hippocampus erectus (Perry, 1810) en diferentes zonas de la costa norte de las regiones occidental y central de la isla. Se llevaron a cabo censos visuales mediante buceo libre, utilizando el método de transectos lineales, entre marzo del 2007 y marzo del 2010. Para la comparación de medias se aplicaron las pruebas de Kruskal Wallis y U de Mann-Whitney. La mayor densidad se encontró en las estructuras artificiales de las estaciones de Barracuda y Caleta, probablemente debido a la gran cantidad de sitios de anclaje presentes y la eutrofización. No se reportaron diferencias en esta variable entre las épocas de lluvia y seca para ninguna de las dos especies. H. reidi fue la especie más abundante y la de mayor distribución. Aunque la densidad de individuos de hipocampos suele ser baja, es posible que la marcada escasez de ejemplares de H. erectus en este caso se deba al método de muestreo (profundidad máxima de 2 metros). Los machos de ambas especies fueron mayores que las hembras. H. reidi se reprodujo todo el año y la proporción sexual registrada fue muy similar a la proporción 1:1, mientras que en H. erectus esta variable fue diferente a la esperada. Las macroalgas del género Caulerpa fueron los sustratos más utilizados por ambas especies.

A geometric morphometric study of a Middle Pleistocene cranium from Hexian, China

The Hexian calvarium is one of the most complete and well-preserved Homo erectus fossils ever found in east Asia, apart from the Zhoukoudian specimens. Various methods bracket the age of the Hexian fossil to between 150 and 412 ka (thousands of years ago). The Hexian calvarium has been considered to be H. erectus given its morphological similarities to Zhoukoudian and Javan H. erectus. However, discussion continues regarding the affinities of the Hexian specimen with other H. erectus fossils. The arguments mainly focus on its relationships to other Asian H. erectus fossils, including those from both China and Java. To better determine the affinities of the Hexian cranium, our study used 3D landmark and semilandmark geometric morphometric techniques and multivariate statistical analyses to quantify the shape of the neurocranium and to compare the Hexian cranium to other H. erectus specimens. The results of this study confirmed the morphological similarities between Hexian and Chinese H. erectus in overall morphology, and particularly in the structure of the frontal bone and the posterior part of the neurocranium. Although the Hexian specimen shows the strongest connection to Chinese H. erectus, the morphology of the lateral neurocranium resembles early Indonesian H. erectus specimens, possibly suggesting shared common ancestry or gene flow from early Indonesian populations. Overall cranial and frontal bone morphology are strongly influenced by geography. Although geographically intermediate between Zhoukoudian and Indonesian H. erectus, the Hexian specimen does not form part of an obvious morphological gradient with regard to overall cranial shape.

Like father, like son: assessment of the morphological affinities of A.L. 288-1 (A. afarensis), Sts 7 (A. africanus) and Omo 119-73-2718 (Australopithecus sp.) through a three-dimensional shape analysis of the shoulder joint.

The postcranial evidence for the Australopithecus genus indicates that australopiths were able bipeds; however, the morphology of the forelimbs and particularly that of the shoulder girdle suggests that they were partially adapted to an arboreal lifestyle. The nature of such arboreal adaptations is still unclear, as are the kind of arboreal behaviors in which australopiths might have engaged. In this study we analyzed the shape of the shoulder joint (proximal humerus and glenoid cavity of the scapula) of three australopith specimens: A.L. 288–1 (A. afarensis), Sts 7 (A. africanus) and Omo 119–73–2718 (Australopithecus sp.) with three-dimensional geometric morphometrics. The morphology of the specimens was compared with that of a wide array of living anthropoid taxa and some additional fossil hominins (the Homo erectus specimen KNM-WT 15000 and the H. neanderthalensis specimen Tabun 1). Our results indicate that A.L. 288–1 shows mosaic traits resembling H. sapiens and Pongo, whereas the Sts 7 shoulder is most similar to the arboreal apes and does not present affinities with H. sapiens. Omo 119–73–2718 exhibits morphological affinities with the more arboreal and partially suspensory New World monkey Lagothrix. The shoulder of the australopith specimens thus shows a combination of primitive and derived traits (humeral globularity, enhancement of internal and external rotation of the joint), related to use of the arm in overhead positions. The genus Homo specimens show overall affinities with H. sapiens at the shoulder, indicating full correspondence of these hominin shoulders with the modern human morphotype.

Combining radiographic and histological data for dental development to compare growth in the past and the present

Background: Being able to estimate the age at death of fossil hominins enables meaningful comparisons of both dental and general growth, past and present.Aim: The aim of this study was to use data for modern permanent canine formation derived from separate histological and radiographic studies to estimate the age at death of an early African Homo erectus specimen (KNM-WT 15 000) with a developing permanent maxillary canine.Methods: Ground sections of 18 sexed modern human canines were used to reconstruct growth in tooth height along the enamel–dentine junction (EDJ) and onwards into root formation along the cement–dentine junction (CDJ). Daily rates of enamel and dentine formation were used to put a time scale to cumulative fractions of tooth height.Results: Age estimates for KNM-WT 15 000 averaged 7.89–8.8 years of age (range = 6.6–10.3 years) and were close to previous histological estimates for this individual (7.6–8.8 years).Conclusions: Stages of dental development in KNM-WT 15 000 were easily accommodated within this age distribution of a modern sample. However, body mass and stature estimates for KNM-WT 15 000 fell well beyond those reported for a modern sample of 438 Sudanese children aged between 7.0–10 years.

Taxonomic differences in deciduous upper second molar crown outlines of Homo sapiens, Homo neanderthalensis and Homo erectus

A significant number of Middle to Late Pleistocene sites contain primarily (and sometimes only) deciduous teeth (e.g., Grotta del Cavallo, Mezmaiskaya, Blombos). Not surprisingly, there has been a recent renewed interest in deciduous dental variation, especially in the context of distinguishing Homo neanderthalensis and Homo sapiens. Most studies of the deciduous dentition of fossil hominins have focused on standard metrical variation but morphological (non-metric and morphometric) variation also promises to shed light on long standing taxonomic questions. This study examines the taxonomic significance of the crown outline of the deciduous upper second molar through principal components analysis and linear discriminant analysis. We examine whether or not the crown shape of the upper deciduous second molar separates H. neanderthalensis from H. sapiens and explore whether it can be used to correctly assign individuals to taxa. It builds on previous studies by focusing on crown rather than cervical outline and by including a large sample of geographically diverse recent human populations. Our samples include 17 H. neanderthalensis, five early H. sapiens, and 12 Upper Paleolithic H. sapiens. In addition, we include two Homo erectus specimens in order to evaluate the polarity of crown shape differences observed between H. neanderthalensis and H. sapiens. Our results show that crown outline shape discriminates H. sapiens and H. neanderthalensis quite well, but does not do well at distinguishing H. erectus from H. sapiens. We conclude that the crown outline shape observed in H. sapiens is a primitive retention and that the skewed shape observed in H. neanderthalensis is a derived condition. Finally, we explore the phylogenetic implications of the results for the H. erectus molars.

Homo erectus and Middle Pleistocene hominins: Brain size, skull form, and species recognition

Hominins that differ from Homo erectus, the Neanderthals, and recent humans are known from Middle Pleistocene localities across the Old World. The taxonomic status of these populations has been clouded by controversy. Perhaps the most critical problem has been an incomplete understanding of variation in skull form. Here, both H. erectus and later mid-Pleistocene hominins are the focus of an investigation aimed at clarifying the relationships among brain volume, basicranial dimensions, neurocranial shape, and certain facial characters. Brain size in H. erectus averages about 950 cm3, while in a series of Middle Pleistocene crania from Africa and Europe, volume is about 1230 cm3. If encephalization is the primary mechanism operating in the mid-Pleistocene, then diverse aspects of cranial form cannot all be treated as independent variables. Correlation is utilized to examine the associations among measurements for more than 30 H. erectus crania that are reasonably well preserved. A similar approach is used with the Middle Pleistocene sample. Patterns of covariation are compared in order to assess integration. Next, factor analysis is applied to the H. erectus specimens in an attempt to identify modules, tightly integrated traits that can evolve independently. Studies of the variation within H. erectus are followed by direct comparisons with the Middle Pleistocene population. Discriminant functions facilitate the description of intergroup differences. Traits that vary independently from brain volume include anterior frontal broadening, lateral expansion of the parietal vault, elevation of the lambda–inion chord, and rounding of the sagittal contour of the occipital. This finding helps to resolve the problem of species recognition. Neurocranial proportions as well as characters from the cranial base and face can be incorporated into a differential diagnosis for the mid-Pleistocene sample. Evidence presented here supports arguments for speciation in the Middle Pleistocene.

Variations and asymmetries in regional brain surface in the genus Homo

Paleoneurology is an important field of research within human evolution studies. Variations in size and shape of an endocast help to differentiate among fossil hominin species whereas endocranial asymmetries are related to behavior and cognitive function. Here we analyse variations of the surface of the frontal, parieto-temporal and occipital lobes among different species of Homo, including 39 fossil hominins, ten fossil anatomically modern Homo sapiens and 100 endocasts of extant modern humans. We also test for the possible asymmetries of these features in a large sample of modern humans and observe individual particularities in the fossil specimens.This study contributes important new information about the brain evolution in the genus Homo. Our results show that the general pattern of surface asymmetry for the different regional brain surfaces in fossil species of Homo does not seem to be different from the pattern described in a large sample of anatomically modern H. sapiens, i.e., the right hemisphere has a larger surface than the left, as do the right frontal, the right parieto-temporal and the left occipital lobes compared with the contra-lateral side. It also appears that Asian Homo erectus specimens are discriminated from all other samples of Homo, including African and Georgian specimens that are also sometimes included in that taxon. The Asian fossils show a significantly smaller relative size of the parietal and temporal lobes. Neandertals and anatomically modern H. sapiens, who share the largest endocranial volume of all hominins, show differences when considering the relative contribution of the frontal, parieto-temporal and occipital lobes. These results illustrate an original variation in the pattern of brain organization in hominins independent of variations in total size. The globularization of the brain and the enlargement of the parietal lobes could be considered derived features observed uniquely in anatomically modern H. sapiens.

Where are inion and endinion? Variations of the exo- and endocranial morphology of the occipital bone during hominin evolution

The occipital bone is frequently investigated in paleoanthropological studies because it has several features that help to differentiate various fossil hominin species. Among these features is the separation between inion and endinion, which has been proposed to be an autapomorphic trait in (Asian) Homo erectus. Methodologies are developed here to quantify for the first time the location of these anatomical points, and to interpret their variation due to the complex interactions between exocranial and endocranial size and shape of the occipital and nuchal planes, as well as the occipital lobes and cerebellum. On the basis of our analysis, neither ‘the separation between inion and endinion’ nor ‘endinion below inion’ can be considered as an autapomorphic trait in H. erectus, since this feature is a condition shared by extant African great apes and fossil hominins. Moreover, our results show that the exo- and endocranial anatomy of the occipital bone differs between hominins (except Paranthropus boisei specimens and KNM-ER 1805) and great apes. For example, chimpanzees and bonobos are characterized by a very high position of inion and their occipital bone shows an antero-posterior compression. However, these features are partly correlated with their small size when compared with hominins. Asian H. erectus specimens have a thick occipital torus, but do not differ from other robust specimens, neither in this feature nor in the analysed exo- and endocranial proportions of the occipital bone. Finally, the apparent brain size reduction during the Late Pleistocene and variation between the sexes in anatomically modern humans (AMH) reflect that specimens with smaller brains have a relatively larger posterior height of the cerebellum. However, this trend is not the sole explanation for the ‘vertical shift’ of endinion above inion that appears occasionally and exclusively in AMH.

Craniometric ratios of microcephaly and LB1,Homo floresiensis, using MRI and endocasts

The designation of Homo floresiensis as a new species derived from an ancient population is controversial, because the type specimen, LB1, might represent a pathological microcephalic modern Homo sapiens. Accordingly, two specific craniometric ratios (relative frontal breadth and cerebellar protrusion) were ascertained in 21 microcephalic infants and children by using MRI. Data on 118 age-equivalent control (normocephalic) subjects were collected for comparative purposes. In addition, the same craniometric ratios were determined on the endocasts of 10 microcephalic individuals, 79 normal controls (anatomically modern humans), and 17 Homo erectus specimens. These ratios were then compared with those of two LB1 endocasts. The findings showed that the calculated cerebral/cerebellar ratios of the LB1 endocast [Falk D, et al. (2007) Proc Natl Acad Sci USA 104:2513-2518] fall outside the range of living normocephalic individuals. The ratios derived from two LB1 endocasts also fall largely outside the range of modern normal human and H. erectus endocasts and within the range of microcephalic endocasts. The findings support but do not prove the contention that LB1 represents a pathological microcephalic Homo sapiens rather than a new species, (i.e., H. floresiensis).

New reconstruction and morphological description of a Homo erectus cranium: Skull IX (Tjg-1993.05) from Sangiran, Central Java

Skull IX (Tjg-1993.05) was unearthed from the upper stratigraphic zone (Bapang-AG levels) of the hominin-bearing sequence in Sangiran. This remarkably complete cranial specimen of Homo erectus from the early Pleistocene of Java preserves substantial portions of the vault and face. However, the distortion present in the original reconstruction has hampered detailed documentation of its morphological characteristics. We here report a new reconstruction of Skull IX that successfully recovers the original morphology and significantly differs from previous reconstructions. Detailed morphological description and the results of initial comparative analyses based on this new reconstruction are provided. The endocranial volume of Skull IX was measured as 870 cc using micro-CT data. The neurocranium of Skull IX is slightly smaller than the so far recorded smallest cranium from this zone, suggesting this individual was female. In most, but not all, aspects of the cranial vault form, details of the external surface structures, and facial morphology, Skull IX exhibits numerous similarities to the other Bapang-AG H. erectus specimens, indicating that it belonged to the Bapang-AG H. erectus population. Drawing on the expanded fossil sample of this chronoregional H. erectus group, we discuss their evolutionary status, degree of sexual dimorphism, and facial morphological variation in Afro-Asian earlier Homo specimens.

Just how strapping was KNM-WT 15000?

For over twenty years, the young, male Homo erectus specimen KNM-WT 15000 has been the focus of studies on growth and development, locomotion, size, sexual dimorphism, skeletal morphology, and encephalization, often serving as the standard for his species. Prior research on KNM-WT 15000 operates under the assumption that H. erectus experienced a modern human life history, including an adolescent growth spurt. However, recent fossil discoveries, improvements in research methods, and new insights into modern human ontogeny suggest that this may not have been the case. In this study, we examine alternative life history trajectories in H. erectus to re-evaluate adult stature estimates for KNM-WT 15000. We constructed a series of hypothetical growth curves by modifying known human and chimpanzee curves, calculating intermediate growth velocities, and shifting the age of onset and completion of growth in stature. We recalculated adult stature for KNM-WT 15000 by increasing stature at death by the percentage of growth remaining in each curve. The curve that most closely matches the life history events experienced by KNM-WT 15000 prior to death indicates that growth in this specimen would have been completed by 12.3 years of age. These results suggest that KNM-WT 15000 would have experienced a growth spurt that had a lower peak velocity and shorter duration than the adolescent growth spurt in modern humans. As a result, it is likely that KNM-WT 15000 would have only attained an adult stature of 163 cm (∼5′4″), not 185 cm (∼6′1″) as previously reported. KNM-WT 15000's smaller stature has important implications for evolutionary scenarios involving early genus Homo.

Hearing ability of the lined seahorse (Hippocampus erectus).

The lined seahorse (Hippocampus erectus), a member of the family Syngnathidae (pipefishes and seahorses), occurs in coastal waters of the western Atlantic, Gulf of Mexico, and Caribbean Sea. This harmless species is listed as “vulnerable” on the International Union for the Conservation of Nature (IUCN) List of Threatened Species, meaning that it has a high risk of extinction in the medium‐term future primarily due to declines in population from targeted catch, bycatch, and degradation of habitat. However, because little is known about hearing in Syngnathids, it is difficult to assess potential effects of anthropogenic sound on these animals. In this study auditory evoked potentials (AEPs) were measured in four H. erectus specimens to determine hearing thresholds and bandwidth. Thresholds were determined using the staircase method with exposures to tone bursts between 50 Hz and 21.6 kHz. At low frequencies H. erectus had AEP thresholds similar to other bony fishes; however, at frequencies above 2 kHz its auditory sensitivity was similar to that of clupeiform species which detect ultrasound [Mann et al., J. Acoust. Soc. Am. (2001)]. The results of this study provide hearing data that can be used to understand potential effects of human‐generated noise on Hippocampus erectus and other seahorse species.

Morphological and morphometric analysis of variation in the Zhoukoudian Homo erectus brain endocasts

The six Zhoukoudian (ZKD) Locality 1 Homo erectus specimens derive from stratigraphic levels 11–3 with a geochronological span of approximately 0.3 Ma. This paper introduces the history of the ZKD endocasts and presents data on their morphological features and linear dimensions in order to evaluate variability in the sample over time and in the broader context of human brain evolution using a comparative sample of African and other Asian H. erectus fossils and modern Chinese males. The ZKD brains are very similar in their morphological characteristics, but there are also significant but subtle changes involving expansion of the frontal and occipital lobe breadths that correlate with the geochronology. The same is not true for general endocranial volume. The ZKD brains, together with other Asian and African H. erectus specimens, have low height dimensions and short parietal chords that distinguish them from the modern Chinese. Furthermore, the lack of geographical patterning in the fossil sample, as determined by Principal Components Analysis, provides no support for arguments advocating the splitting of H. erectus into separate taxa.

Relative limb strength and locomotion in Homo habilis

The Homo habilis OH 62 partial skeleton has played an important, although controversial role in interpretations of early Homo locomotor behavior. Past interpretive problems stemmed from uncertain bone length estimates and comparisons using external bone breadth proportions, which do not clearly distinguish between modern humans and apes. Here, true cross-sectional bone strength measurements of the OH 62 femur and humerus are compared with those of modern humans and chimpanzees, as well as two early H. erectus specimens-KNM-WT 15000 and KNM-ER 1808. The comparative sections include two locations in the femur and two in the humerus in order to encompass the range of possible section positions in the OH 62 specimens. For each combination of section locations, femoral to humeral strength proportions of OH 62 fall below the 95% confidence interval of modern humans, and for most comparisons, within the 95% confidence interval of chimpanzees. In contrast, the two H. erectus specimens both fall within or even above the modern human distributions. This indicates that load distribution between the limbs, and by implication, locomotor behavior, was significantly different in H. habilis from that of H. erectus and modern humans. When considered with other postcranial evidence, the most likely interpretation is that H. habilis, although bipedal when terrestrial, still engaged in frequent arboreal behavior, while H. erectus was a completely committed terrestrial biped. This adds to the evidence that H. habilis (sensu stricto) and H. erectus represent ecologically distinct, parallel lineages during the early Pleistocene.

Femoral/humeral strength in early African Homo erectus

Lower-to-upper limb-bone proportions give valuable clues to locomotor behavior in fossil taxa. However, to date only external linear dimensions have been included in such analyses of early hominins. In this study, cross-sectional measures of femoral and humeral diaphyseal strength are determined for the two most complete early Homo erectus (or ergaster) associated skeletons—the juvenile KNM-WT 15000 and the adult KNM-ER 1808. Modern comparative samples include an adult human skeletal sample representative of diverse body shapes, a human longitudinal growth series, and an adult chimpanzee sample. When compared to appropriately age-matched samples, both H. erectus specimens fall very close to modern human mean proportions and far from chimpanzee proportions (which do not overlap with those of humans). This implies very similar mechanical load-sharing between the lower and upper limbs, and by implication, similar locomotor behavior in early H. erectus and modern humans. Thus, by the earliest Pleistocene (1.7 Ma), completely modern patterns of bipedal behavior were fully established in at least one early hominin taxon.