Print version ISSN 0038-2353
S. Afr. j. sci. vol.103 n.7-8 Pretoria Jul./Aug. 2007
D.D. StynderI, II, *; R.R. AckermannI; J.C. SealyI
IDepartment of Archaeology, University of Cape Town, Private Bag X3, Rondebosch 7701, South Africa
IILaboratoire d'Anthropobiologie, Université Paul Sabatier, 39 allées Jules Guesde, 31000 Toulouse, France
The sample of South African early to mid-Holocene Later Stone Age(LSA) human crania is small and quite fragmentary, limiting our knowledge of human craniofacial morphology for this period. Previous limited analyses have described the morphology displayed by these early crania as a combination of Khoesan and non-Khoesan traits. Although essentially Khoesan-like in terms of facial morphology, their overall large size and robust neurocranial structure were regarded as atypical of Khoesan craniofacial morphology, leading to questions about the role of these early populations in the ancestry of recent Khoesan populations. Here we provide a quantitative analysis in which we compare five well-preserved pre-5000 BP LSA crania with (i) a large sample of post-5000 BP LSA Khoesan crania; and (ii) a sample of crania from recent South African Bantu-speakers. We show that these pre-5000 BP crania fall comfortably within the range of variation observed for the post-5000 BP Khoesan sample, in terms of both size and shape, suggesting that distinctive Khoesan craniofacial morphology was already present in South African LSA populations by the first half of the Holocene.
Khoesan is a term used to identify a large cluster of southern African peoples who share a number of linguistic, cultural and biological traits which distinguish them from neighbouring Bantu-speakers.1,2 Although linguistically diverse, all Khoesan groups speak click languages.3,4 Similarities in territorial organization, gender relations, kinship, ritual and cosmology are also shared across all Khoesan groups.2 Biologically, the Khoesan exhibit a number of morphological characteristics such as light yellow-brown skin, epicanthic eyefolds and female steatopygia, that are unique among southern African populations.2,5
The Khoesan possess some of the deepest genetic roots of all recent humans, possibly reaching as far back as the early Late Pleistocene.6,7 In contrast, their distinctive phenotype appears to have had a much more recent origin. Late Pleistocene South African fossils, such as the c. 110 00090 000-year-old Klasies River specimens and the c. 80 00055 000-year-old Border Cave specimens, cannot be securely assigned to any contemporary African population, let alone to the Khoesan, on the basis of craniofacial traits.812 The more recent Hofmeyr cranium (ELM 24; c. 36 000 years old) also does not resemble the craniofacial pattern of recent Khoesan peoples.13
On current evidence, the earliest appearance of Khoesan-like craniofacial traits in South African human populations likely dates back to the terminal Pleistocene or early Holocene. Analyses of the 'Fish Hoek Man' cranium (SAM-AP 4692), reportedly dated to c. 12 000 BP, indicate a close resemblance to recent Khoesan peoples.1419 However, a secure date for SAM-AP 4692 is not yet available, and therefore this specimen cannot at this stage provide firm support for a terminal Pleistocene age for the appearance of characteristic Khoesan craniofacial traits.
The earliest securely dated cranium which displays close morphological affinities to Khoesan crania is the terminal Pleistocene/early Holocene 'Albany Man' cranium (UCT 378) from Elands Bay Cave on the Cape southwest coast (Table 1).18,20 In addition to UCT 378, systematic excavations in 1978 produced a second fragmentary, early Holocene cranium, UCT 374 (Table 1).18,20 Bräuer and Rösing18 note that UCT 378 combines large overall size and robusticity with typical Khoesan facial morphology. UCT 374 has thus far not been described in the literature.
The site of Matjes River Rock Shelter in the southern Cape has also produced several fragmentary human crania from its terminal Pleistocene/early Holocene Layer D.21,22 Unfortunately, only one individual from this layer, NMB 1342 (also designated MR 1), has been securely dated to the terminal Pleistocene/early Holocene (Table 1).22,23,27 Like UCT 378, NMB 1342 is a large, robust cranium which displays characteristic Khoesan facial morphology. The other fragmentary crania from Layer D display similar robust Khoesan-like morphology.18
Wilton Large Rock Shelter in the Eastern Cape and Oakhurst Cave in the southern Cape produced securely dated crania from the first half of the Holocene (Table 1).2427 Although belonging to a sub-adult, ALB 119 from Wilton Large Rock Shelter, resembles crania from Elands Bay Cave and Matjes River Layer D in terms of combining Khoesan facial form with overall large size and robusticity.18 Unfortunately, the crania from Oakhurst have not previously been analysed from a morphological perspective. We include one cranium from this site, UCT 180, in our analysis.
Braüer and Rösing18 have argued that although many of these early crania display Khoesan-like facial morphology, their large overall size and robusticity apparently distinguishes them from more recent Khoesan crania. It has even been suggested that their greater size and robusticity may align them with Bantu-speakers rather than with the Khoesan.18,28 There has, however, never been an adequate investigation of the purported distinctiveness of early to mid-Holocene South African crania. The fragmentary nature of this cranial sample and the absence of a comparative cranial sample which adequately represents the range of morphological variation present in Khoesan populations stifled previous attempts to address this issue. It is in this context that we present a metrical comparison between five, well-preserved, pre-5000 BP LSA crania (four of which have recently been directly dated for the first time), a sample of post-5000 BP LSA Khoesan crania, and a cranial sample from recent Bantu-speakers.
Materials and methods
Adult status and sex were determined on the basis of a combination of cranial and, when available, postcranial morphological characteristics.29,30 The five pre-5000 BP crania analysed all belong to males. Accession numbers, localities, dates and dating laboratory numbers for these crania are provided in Table 1. The crania which made up the post-5000 BP LSA Khoesan sample (n = 100) was composed of individually dated male crania from the western, southwestern, southern and southeastern coasts and coastal forelands of South Africa.19,31 A comparative Bantu-speaker cranial sample (n = 50) was composed of recent cadaver-derived male crania from the Raymond A. Dart Collection of Human Skeletons, University of the Witwatersrand, Johannesburg.
Three-dimensional coordinates of 20 cranial landmarks were recorded on the left side of each cranium (Table 2) using a MicroscribeTM 3-D digitizer and InScribe-32 software (Immersion Corp., San Jose, CA). Most landmarks were of homology type I, according to the criteria of Bookstein.32 Four were of type II (P, O, BA, MXT) and two were of type III (1/2BN, 1/2BL). Homology type I concerns discrete juxtapositions of tissues (points in space where two or three structures meet, such as cranial sutures) and have the highest rates of reproducibility; homology type II concerns maxima of curvatures of morphogenetic processes (e.g. the glabella); and homology type III concerns constructed landmarks (e.g. midpoints between two landmarks). Prior to analysis, coordinate data were transformed into linear data, and a subset of 48 variables was selected to represent overall cranial morphology without redundancy (Table 3).
Principal components analysis (PCA)33,34 was used to investigate the morphological affinities of the pre-5000 BP sample and also to characterize their primary morphological traits. All analyses were carried out on untransformed data (preserving size). The computation of the principal components (PCs) was done via the correlation matrix. PCA has the advantage of being able to reduce a large data set of (possibly) correlated variables into a (smaller) number of uncorrelated variables, the PCs. Analysing the PCs makes it easier to identify meaningful underlying variables that distinguish crania from one another. PCs may be plotted against each other, to visualize morphological relationships. Specimens that are morphologically similar occupy similar multivariate space. PCA is particularly useful in the context of this study in that it allows for the evaluation of size and size-related shape variation within the study sample. In biological studies, the first principal component commonly reflects variation in size and size-related shape. One can determine whether the crania of pre-5000 BP people were significantly larger than those of later Khoesan people by analysing the first principal component.
Table 4 presents the eigenvectors for the first three PCs (see supplementary material online). The component loadings on the first PC are all positive, confirming that this reflects size-related variation. In Figs 1a and 1b, the component scores for the first three PCs are plotted against each other. In both plots, 95% confidence ellipses are constructed around the post-5000 BP and Bantu-speaker samples. PC 1 represents size and size-related shape variation. The most positive values along PC 1 represent large crania characterized by long/broad faces and prognathic maxillary regions. The most negative values represent small crania, characterized by short/narrow faces and orthognathic maxillary regions. The most positive values along PC 2 represent crania characterized by reduced frontal heights, lengths and breadths, and retracted upper-facial regions. The most negative values represent crania characterized by increased frontal heights, lengths and breadths, and projecting upper-facial regions. The most positive values along PC 3 represent crania characterized by increased frontal heights, lengths and breadths, reduced facial heights, and increased neurocranial lengths and posterior neurocranial heights. The most negative values represent crania characterized by reduced frontal heights, lengths and breadths, increased facial heights and reduced neurocranial lengths and posterior neurocranial heights. Although there are overlaps along both PCs in Fig. 1a, it is evident that crania in the post-5000 BP sample are generally smaller than crania in the Bantu-speaker sample, and are characterized by shorter/narrower faces and less prognathic maxillary regions (PC 1). Post-5000 BP crania are also characterized by increased frontal heights, lengths and breadths, and more projecting upper-facial regions, while crania in the Bantu-speaker sample display the opposite trend. All five pre-5000 BP crania fall well within the 95% confidence ellipse of the post-5000 BP cranial sample, while three (UCT 180, SAM-AP 5055, UCT 156) fall outside the range of variation of the Bantu-speaker sample. Their positions along PC 1 indicate that they are relatively large and possess relatively longer/broader faces and more prognathic maxillary regions than the majority of post-5000 BP crania. They are indistinguishable from the Bantu-speaker comparative sample along this PC. Their positions along PC 2 indicate that they are characterized by increased frontal heights, lengths and breadths and projecting upper-facial regions. These traits distinguish them from the majority of the Bantu-speaker sample and align them with the post-5000 BP LSA sample. In Fig. 1b, all five pre-5000 BP crania again fall within the range of variation of the post-5000 BP sample, with four (UCT 180, SAM-AP 4182, SAM-AP 5055, UCT 156) falling outside the range of variation of the Bantu-speaker sample. The earliest cranium in the pre-5000 BP sample, UCT 156, falls on the edge of the 95% confidence ellipse of the post-5000 BP sample, reflecting a combination of large frontal region, projecting upper-facial region, reduced facial height and increased neurocranial length.
Discussion and conclusion
With only five pre-5000 BP LSA crania available, sample size is an obvious problem when it comes to interpreting the results of this study. A larger sample would be desirable because it would better reflect the original variation of this early population. However, it is very rare that Pleistocene and early Holocene human skeletal material is found in adequate quantities to be truly representative of the original variation of an ancient population. The results should be taken with caution, bearing this limitation in mind. Nevertheless, the available sample does allow for certain preliminary deductions.
The current study confirms previous observations that early to mid-Holocene South African human crania resemble those of more recent Khoesan populations in terms of facial shape.18 Although these early crania are relatively large, they fall well within the range of variation of late Holocene LSA Khoesan crania, in terms of both size and primary shape variation. This contradicts an earlier assertion that early to mid-Holocene populations possessed significantly larger crania than recent Khoesan.18 The individuals studied here also fall outside or on the edge of the range of variation of a recent Bantu-speaker comparative sample, further confirming their Khoesan affinities.
It has been suggested that early to mid-Holocene South Africans differed from later Khoesan people in terms of possessing more robust crania.18 Although the current study does not specifically investigate robusticity, it is known that robusticity is strongly correlated with cranial size.35 Since cranial size during the South African early to mid-Holocene appears to have been quite large, it comes as no surprise that early crania were also quite robust. Some late Holocene LSA crania also display a combination of large overall size and high levels of robusticity.19,31 High levels of robusticity are thus also not unique to the early sample.
The contradiction between the results of this study and the observations of Bräuer and Rösing18 can be explained. When Bräuer and Rösing18 performed their study, very little was known about craniofacial variation in Khoesan populations during the Holocene. This was primarily due to the poorly dated LSA skeletal sample.18,36 Today, we have access to a large, well-dated South African LSA cranial sample which extends across most of the Holocene.19, 31 We are thus in a better position to analyse cranial morphology at specific times during the Holocene.31
This study showed that early to mid-Holocene South African populations already possessed distinctly Khoesan craniofacial morphology. Although results indicate that the Khoesan phenotype was already present at the start of the Holocene, we are currently not in a position to determine when it actually originated. As has been stated, the c. 36 000-year-old Hofmeyr cranium does not display Khoesan morphology. The Khoesan phenotype must thus have originated sometime after c. 36 000 years ago, during the terminal Pleistocene, a hypothesis previously suggested by Morris.37,38 Unfortunately, there is no securely dated, complete cranium from this period currently available to confirm this hypothesis. Nevertheless, a probable terminal Pleistocene origin for the Khoesan phenotype marks them as one of the few contemporary human populations whose morphological origins pre-date the advent of the Holocene. On current evidence, the craniofacial traits which characterize contemporary Chinese, European and Native American populations only appeared to have developed during the course of the Holocene.3941
We thank the curators of the osteological collections, at which data were acquired, for access to their specimens. The South African Heritage Resources Agency (SAHRA) provided the permits to date the crania used in this study, which was sponsored by the Wenner-Gren Foundation for Anthropological Research (D.D.S., grant number Gr. 7038); the Palaeo-Anthropology Scientific Trust (D.D.S.); and the National Research Foundation (R.R.A., J.C.S.).
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Received 18 May. Accepted 9 August 2007.
Supplementary material to:
Stynder D.D., Ackermann R.R. and Sealy J.C. (2007). Early to mid-Holocene South African Later Stone Age human crania exhibit a distinctly Khoesan morphological pattern. S. Afr. J. Sci. 103, 349352.