Unraveling hominin behavior at another anthropogenic site from Olduvai Gorge (Tanzania): new archaeological and taphonomic research at BK, Upper Bed II

New archaeological excavations and research at BK, Upper Bed II (Olduvai Gorge, Tanzania) have yielded a rich and unbiased collection of fossil bones. These new excavations show that BK is a stratified deposit formed in a riverine setting close to an alluvial plain. The present taphonomic study reveals the second-largest collection of hominin-modified bones from Olduvai, with abundant cut marks found on most of the anatomical areas preserved. Meat and marrow exploitation is reconstructed using the taphonomic signatures left on the bones by hominins. Highly cut-marked long limb shafts, especially those of upper limb bones, suggest that hominins at BK were actively engaged in acquiring small and middle-sized animals using strategies other than passive scavenging. The exploitation of large-sized game (Pelorovis) by Lower Pleistocene hominins, as suggested by previous researchers, is supported by the present study.     

Crocodylian and mammalian carnivore feeding traces on hominid fossils from FLK 22 and FLK NN 3, Plio-Pleistocene, Olduvai Gorge, Tanzania

Taphonomic analysis of the Olduvai Hominid (OH) 8 left foot from FLK NN Level 3 and the OH 35 left leg from FLK Level 22 (Zinjanthropus level) in Middle Bed I, Olduvai Gorge, indicates that both were fed upon by crocodiles. Both bear extensive tooth marking, including bisected tooth marks diagnostic of crocodylian feeding. The location of the bisected tooth marks on the distal tibia and the talus indicates disarticulation of the foot by crocodiles. The broken proximal ends of the tibia and fibula are more typical of feeding by a leopard-like carnivore, as is damage to the OH 7 mandible and parietals that are associated with and may derive from the same individual as OH 8. Previous work showing a close articulation of the foot and the leg has been used to suggest that the two specimens belong to the same individual despite deriving from sites separated by 200 m and slightly different stratigraphic levels according to previous work. The location and agent of tooth marking and the nature of gross damage do not refute this hypothesis, but the punctures on the talus and distal tibia differ in size and sharpness. Recent work shows that the stratigraphic discrepancy between OH 8 and OH 35 is greater than previously thought, refuting the single-individual hypothesis. Although seemingly unlikely, this denotes that two hominids represented by rarely found leg and foot elements both lost their left foot to crocodiles at nearby sites within a 6,000 year interval. We cannot determine if the hominids were preyed upon by crocodiles or mammalian carnivores. However, the carnivore damage to them and associated faunal remains suggests that high predation risk constrained hominid activities involving discard of the stone artifacts found at these sites. This finding is inconsistent with the interpretation of the sites as home bases or living floors.     

Tool-using strategies by early hominids at bed II, Olduvai Gorge, Tanzania

This study examines the current prevailing model of Oldowan technology-the opportunistic, least-effort strategy of stone tool making and using by early hominids. The sample includes the MNK chert factory site and three contemporaneous assemblages from Olduvai Gorge, all dated between 1.65 and 1.53 m.y.a. The analysis suggests that early hominids at Olduvai may have been selective, applying distinctive strategies in making and using tools depending on the different types of raw materials available to them. The preponderance of lava cores and near absence of flakes associated with the cores suggest that lava cores at Olduvai did not provide a source of flakes. They were primarily heavy-duty core tools, despite the fact that the majority of Olduvai lava is of excellent quality for flaking. Contrary to this pattern, the abundance of chert flakes and the lack of large chert cores suggest that the production of flakes was the most important strategy applied to chert. Original forms and flaking mechanics of the raw materials may have been important factors in the simultaneous application of the different, complementary strategies. The Oldowan tool-using strategy was dynamic and flexible, in response to changes in raw material availability. The use of chert between 1.65 and 1.53 m.y.a. was apparently related to the drastic decrease in flake production in lava and quartz. Finally, lack of initial reduction episodes of lava material challenges the idea of the stone cache strategy at Olduvai between 1.65 to 1.53 m.y.a.     

A diagnosis of crocodile feeding traces on larger mammal bone, with fossil examples from the Plio-Pleistocene Olduvai Basin, Tanzania

Neotaphonomic studies have determined the patterns of bone damage created by larger mammalian carnivores when consuming mammalian carcasses. Typically, mammalian carnivores gnaw and break bones to various degrees in order to access marrow, grease, and brain tissue. In contrast, crocodiles attempt to swallow whole parts of mammal carcasses, inflicting in the process tooth marks and other feeding traces on some of the bones they are unable to ingest. Although crocodiles are major predators of larger mammals along the margins of protected tropical rivers and lakes, their feeding traces on bone have received little systematic attention in neotaphonomic research. We present diagnostic characteristics of Crocodylus niloticus damage to uningested mammal bones resulting from a series of controlled observations of captive crocodile feeding. The resulting bone assemblages are composed of primarily complete elements from articulating units, some of which bear an extremely high density of shallow to deep, transversely to obliquely oriented tooth scores over often large areas of the bone, along with shallow to deep pits and punctures. Some of the tooth marks (bisected pits and punctures, hook scores) have a distinctive morphology we have not observed to be produced by mammalian carnivores. The assemblages are also characterized by the retention of both low- and high-density bone portions, an absence of gross gnawing, and minimal fragmentation. Together, the damage characteristics associated with feeding by crocodiles are highly distinctive from those produced by mammalian carnivores. Modern surface bone assemblages along the Grumeti River in Tanzania's Serengeti National Park contain a mixture of specimens bearing damage characteristic of crocodiles and mammalian carnivores. Comparison of Plio-Pleistocene fossil bones from Olduvai Gorge, Tanzania, to bones damaged by captive and free-ranging Nile crocodiles reveals direct evidence of fossil crocodilian feeding from larger mammal bones associated with Oldowan stone artifacts.     

Archaeological predictions for hominid land use in the paleo-Olduvai Basin, Tanzania, during lowermost Bed II times

We present a preliminary predictive model of Oldowan stone artefact and scavenged larger mammal bone assemblages for 11 landscape facets modeled earlier to occur across a large portion (>300 km²) of the paleo-Olduvai Basin during lowermost Bed II times. This second phase of model-building is based on our earlier characterizations of the basin's landscape ecostructure and the inter-facet distribution of key resources and hazards probably encountered by Late Pliocene hominids (Peters & Blumenschine, 1995, 1996). Our current extension of the model of hominid–landscape interactions specifies additional theoretical components, including: (1) the assumed capabilities of Oldowan hominids (presumablyHomo habilis, primarily); (2) the landscape-facet-specific tasks they carried out; (3) the immediate stone and bone task residues they produced; and (4) the predicted composition, condition, density, and clustering of stone artefact and butchered and unbutchered bone assemblages for each facet. We develop ecological linkages between these new and formerly reported modeling components, the most fundamental of which is the facet-specific degree of tree/shrub cover abundance, and the correlated degree of competition among larger carnivores and hominids for scavengeable larger mammal carcasses. These factors condition variability among landscape facets in scavenging opportunities encountered by hominids, which in our model is the major predictor of bone and stone artefact assemblage composition. The predictive value of scavenging reflects the bias of paleoanthropological traces toward technology and butchery in their landscape context, but the model is surprisingly insensitive to what are usually thought to be critical social components of hominid land use. The predictions for the traces of hominid–landscape interactions modeled herein can be tested in the future against the landscape archaeological sample being excavated from lowermost Bed II by the Olduvai Landscape Paleoanthropology Project.     

Fine resolution of early hominin time, Beds I and II, Olduvai Gorge, Tanzania

Reconstructing paleoenvironments and landscapes within lake-centered, hominin-yielding basinal sequences requires a resolution of time-rock units finer than but complementary to that provided by the present tephrostratigraphy. Although indispensable in providing an absolute time frame at Olduvai, the average 15,000-20,000 year intervals between successive tuff units lack the time resolution to construct a sufficiently contemporary paleolandscape within sedimentary intervals away from the interleaved tuffs. Such control is essential to construct valid paleogeographies in which to contextualize contemporaneous paleoanthropological sites and the traces of hominin land use they contain. Within Beds I and II of the Olduvai Basin a Sequence Stratigraphic analysis has achieved a relative time framework in which time-rock units, “lake-parasequences,” each generated by a major advance and withdrawal of the lake system, are recognizable for average periods of about 4000 years duration. Within each of these time slices at least two paleogeographic landscapes are identifiable, reducing the time constraints of an individual landscape reconstruction to a few thousand years. Within the sedimentary succession both highly incised and less incised unconformities are identifiable to provide sequence boundaries. Within each sequence the higher frequency lake-parasequences can be identified by (1) a disconformable base, (2) accretion of sediment during lake transgression and at maximum, (3) a disconformable top caused by lake withdrawal, and (4) a soil profile generated beneath that disconformable land surface. Individual lake-parasequences can be recognized in lake marginal and fan settings, and their imprint can also be seen in the lake setting where, for example, maximum flooding might be marked by a layer of dolomite. Lower Bed II parasequences represent time intervals of <5000 years, while parasequential periods between Tuffs IB and IC in Bed I are <4300 years. Analogous Holocene lake-level changes of the same order in East Africa have a period close to 4200 years. The estimated period is close to that defined by Stadial/Interstadial Dansgaard-Oeschger Events recorded in the Greenland Ice record, which force cycles of period similar to lake-parasequences, both in the Arabian Sea and Lake Malawi. Lake-parasequences not only aid construction of landscapes, they also allow contextualization of individual paleoanthropological occurrences. For instance, a parasequence lies between Leakey’s Level 1 and her butchered Deinotherium occurrence at FLK N. However, elephantid and giraffid skeletons associated with stone artifacts at VEK, uncovered by OLAPP excavations, are situated on the same land surface as a possibly butchered rhinocerid at KK. To complement the existing absolute radiometric time framework, relative Sequence Stratigraphic techniques might be applied to any lake-centered, hominin-yielding basinal sequence, not only those found within East Africa. Because they are climatically controlled, and might plausibly be related to globally driven Dansgaard-Oeschger Events, lake-parasequences and their associated sequences might be correlatable between various East African basins in the Plio-Pleistocene in the same way as they presently are for the Holocene.     

Environments and hominin activities across the FLK Peninsula during Zinjanthropus times (1.84 Ma), Olduvai Gorge, Tanzania

We establish through 13 excavations the landscape context and nature of hominin activities across the Zinjanthropus land surface from which the Leakeys recovered the FLK 22 and FLK NN 1 paleoanthropological assemblages. The land surface was created by fluvial incision of the eastern margin of paleo-Lake Olduvai following a major lake withdrawal. Erosion was uneven, leaving a peninsula bounded by a river channel, the FLK Fault, and a freshwater wetland. This FLK Peninsula supported groves of trees that attracted hominins and carnivores, and that preserved the dense concentrations of carcass remains and stone tools they left behind, including those at FLK 22. Some carcasses appear to have been acquired at the ecotone of the Peninsula and Wetland, where another dense artifact and bone assemblage accumulated. A lesser topographic high at the edge of a Typha marsh in the Wetland was the site of FLK NN 1 and a scatter of large stone tools used possibly for rootstock processing.Our landscape reconstruction delimits the vegetation mosaic indicated by previous work and provides a topographical explanation for the existence of FLK 22 and FLK NN 1. Both are unexpected if the FLK area was the flat, featureless lake margin terrain typical of lake basins similar to paleo-Olduvai. The results show that the Leakeys’ sites were not isolated occupation floors but rather parts of a land surface utilized intensively by hominins. Although commonly considered to have been home bases, their likely high predation risk, evidenced by large carnivore feeding traces and the remains of four hominin individuals, suggests visits to them were brief and limited to feeding. Finally, stratigraphic observations confirm that FLK NN 3 accumulated on an older land surface, refuting the hypothesis that the OH 8 foot found there is the same individual as the OH 35 leg from FLK 22.     

Tracks,Trails and Trampling by Large Vertebrates in a Rift Valley Paleo-Wetland,Lowermost Bed II,Olduvai Gorge,Tanzania

The impact of large vertebrates on the sedimentary record in an East African groundwater-fed wetland in Ngorongoro Crater, Tanzania, is used as a modern analog to interpret an ancient (Plio-Pleistocene) wetland record in Olduvai Gorge, Tanzania. The 3 km² wetland at Olduvai is characterized by massive silty claystones produced by intense vertebrate trampling, as well as trails by vertebrates frequenting the wetlands and isolated footprints that represent a “snapshot in time.” Based on modern analogs, a paleo hippo trail (1.2 m wide and 0.6 m deep) in the Plio-Pleistocene wetlands is interpreted as a frequently used corridor between hippo pools (days) and grazing meadows (nights). Groundwater-fed wetlands are low energy environments where the physical record appears to be dominated by plant and animal activity. The bioturbation record reflects a number of interacting factors such as substrate texture, moisture content, sedimentation rate, frequency of flooding, type of animals present, trampling rate, and post-depositional changes (compaction). Lithofacies in both the modern and ancient wetlands include muddy sandstone (drainage channels) and silty claystone (vegetated and nonvegetated mud flats). Organic-rich sediments eventually oxidize, eliminating most evidence of the habitat. Modern wetlands have organic-rich mud and peat, whereas the ancient analog has siliceous earthy claystones that contains plant remains, bone fragments, pollen, phytoliths, and localized beds of diatomite. Thus, the physical record of vertebrate bioturbation in conjunction with paleontological and lithological records provides crucial information on the ecology of ancient wetland environments.