Journal of Human Evolution 55 (2008) 652–664
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Journal of Human Evolution
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The Middle Stone Age of the northern Kenyan Rift: age and context of new archaeological sites from the Kapedo Tuffs
Christian A. Tryon a,*, Neil T. Roach b, M. Amelia V. Logan c a Human Origins Program, Department of Anthropology, National Museum of Natural History, Smithsonian Institution, PO Box 37012, MRC 112, Washington DC, 20013-7012, USA b Department of Anthropology, Harvard University, Cambridge MA, 02138, USA c Department of Mineral Sciences, National Museum of Natural History, Smithsonian Institution, PO Box 37012, MRC 119, Washington DC, 20013-7012, USA article info abstract
Article history: Rift Valley sites in southern Ethiopia and northern Kenya preserve the oldest fossil remains attributed to Received 22 June 2007 Homo sapiens and the earliest archaeological sites attributed to the Middle Stone Age (MSA). New Accepted 14 March 2008 localities from the Kapedo Tuffs augment the sparse sample of MSA sites from the northern Kenya Rift. Tephrostratigraphic correlation with dated pyroclastic deposits from the adjacent volcano Silali suggests an age range of 135–123 ka for archaeological sites of the Kapedo Tuffs. Comparisons of the Kapedo Tuffs Keywords: archaeological assemblages with those from the adjacent Turkana and Baringo basins show broad lithic Tephrostratigraphy technological similarity but reveal that stone raw material availability is a key factor in explaining Silali Lithic technology typologically defined archaeological variability within this region. Spatially and temporally resolved Regional variation comparisons such as this provide the best means to link the biological and behavioral variation manifest Middle-Late Pleistocene in the record of early Homo sapiens. Ó 2008 Elsevier Ltd. All rights reserved.
Introduction between biological and behavioral variation among geographically diverse hominin populations within (and outside of) Africa requires Fossil and genetic data support an eastern African origin for an integration of genetic, fossil, archaeological, and paleoenvir- Homo sapiens some time in the later part of the middle Pleistocene, onmental data at fine temporal and spatial scales (e.g., Barham, 195 ka (White et al., 2003; McDougall et al., 2005; Gonder et al., 2001; Potts, 2002; Gamble et al., 2005; James and Petraglia, 2005; 2007). Rather than focus on species-level distinctions or ‘‘modern/ Banks et al., 2006; Vanhaeren and d’Errico, 2006). nonmodern’’ contrasts, a number of recent studies have empha- We describe here one small step towards achieving our long sized the diversity among populations of middle and late Pleisto- term goal of understanding temporal and spatial variation among cene hominins in Africa and elsewhere, particularly in the mosaic of African middle and late Pleistocene hominin populations that primitive and derived features, life history traits, and complex included Homo sapiens, and report our recent discovery of five new mitochondrial and nuclear DNA signatures (e.g., Lahr and Foley, MSA artifact localities from the Kapedo Tuffs. These sites are likely 1998; Howell, 1999; Forster, 2004; Eswaran et al., 2005; Trinkaus, constrained to a narrow temporal window between 135 ka and 2005; Smith et al., 2007). In Africa, the archaeological record of this 123 ka, and occur in the northern Kenya Rift Valley between the period is characterized by the replacement of the Acheulian by better studied Turkana and Baringo basins. The area between these Middle Stone Age (MSA) sites that preserve the first evidence for basins is particularly important for understanding human bio- subcontinental-scale regional variation (Clark, 1988; McBrearty and cultural evolution, but which until now has not been the subject of Brooks, 2000; McBrearty and Tryon, 2006), mirroring a broader detailed paleoanthropological investigation. The Turkana Basin phenomenon of post-Acheulian diversification of the archaeologi- preserves the fossil remains of the earliest Homo sapiens cal record also seen in Europe and western Asia (e.g., Ronen and (McDougall et al., 2005), and the Baringo Basin preserves some of Weinstein-Evron, 2000; Soressi, 2004, 2005; Hovers and Kuhn, the oldest known MSA sites (Deino and McBrearty, 2002; Tryon and 2006; see also Gao and Norton, 2002). Exploring the relation McBrearty, 2002, 2006; McBrearty and Tryon, 2006). As the Kapedo Tuffs represent a new artifact-bearing area, we first describe their geological setting, estimated age determined through tephros- * Corresponding author. Mailing address: Department of Anthropology, New York tratigraphic correlation, and the composition of all recovered arti- University, 25 Waverly Place, New York, NY 10003, USA. E-mail addresses: [email protected] (C.A. Tryon), [email protected] (N.T. fact assemblages. We then integrate these data from the Kapedo Roach), [email protected] (M.A.V. Logan). Tuffs into a comparison of archaeological data from neighboring
0047-2484/$ – see front matter Ó 2008 Elsevier Ltd. All rights reserved. doi:10.1016/j.jhevol.2008.03.008 C.A. Tryon et al. / Journal of Human Evolution 55 (2008) 652–664 653
depositional basins to initiate studies of geographic variation in Mecca hominin behavior among MSA sites in this area. Our comparisons of Kibish Formation MSA artifacts from the Kapedo Tuffs, Turkana Basin, and Baringo Basin emphasize the role of stone raw material as an explanation Addis Abeba for interassemblage differences among these areas, and serve to 5°N highlight environmental factors that affect a number of stone tool mo River O assemblage attributes that are frequently used to interpret pop- Nairobi ulation-specific behavioral variation at Pleistocene sites. Indian Ocean Chow Behir
The Kapedo Tuffs and Silali