Examining time trends in the Oldowan technology at Beds I and II,Olduvai Gorge

The lithic analysis of the Bed I and II assemblages from Olduvai Gorge reveals both static and dynamic time trends in early hominids' technology from 1.8 to 1.2 m.y.a. The Bed I Oldowan (1.87-1.75 m.y.a.) is characterized by the least effort strategy in terms of raw material exploitation and tool production. The inclusion of new raw material, chert, for toolmaking in the following Developed Oldowan A (DOA, 1.65-1.53 m.y.a.) facilitated more distinctive and variable flaking strategies depending on the kind of raw materials. The unique characters of DOA are explainable by this raw material factor, rather than technological development of hominids. The disappearance of chert in the subsequent Developed Oldowan B and Acheulian (1.53-1.2 m.y.a.) necessitated a shift in tool production strategy more similar to that of Bed I Oldowan than DOA. However, the evidence suggests that Bed II hominids might have been more skillful toolmakers, intensive tool-users, and engaged in more active transport of stone tools than the Bed I predecessors. Koobi Fora hominids maintained a more static tool-using behavior than their Olduvai counterparts due mainly to a stable supply of raw materials. They differed from Olduvai hominids in terms of less battering of cores, consistent transport behavior, and few productions of side-struck flakes, indicating a regional variation of toolmaking and using practice. However, they shared with Olduvai hominids a temporal trend toward the production of larger flakes from larger cores after 1.6 m.y.a. Increased intake of animal resources and the expansion of ranging area of Homo ergaster would have led to the development of technological organization. Technological changes in the Oldowan industry are attested at Olduvai Gorge, Koobi Fora, and Sterkfontein, suggesting that it was a pan-African synchronous phenomenon, beginning at 1.5 m.y.a.     

Disentangling Early Stone Age palimpsests: determining the functional independence of hominid- and carnivore-derived portions of archaeofaunas

Determining the extent to which hominid- and carnivore-derived components of fossil bone palimpsests formed independently of each other can provide valuable information to paleoanthropologists interested in reconstructing the foraging adaptations of hominids. Because stone tool cutmarks, hammerstone percussion marks, and carnivore tooth marks are usually only imparted on bone during nutrient extraction from a carcass, these bone surface modifications are particularly amenable to the types of analyses that might meet this goal. This study compares the percentage of limb bone specimens that preserve evidence of both hominid- and carnivore-imparted bone damage from actualistic control samples and several Plio-Pleistocene archaeofaunas, including new data from Swartkrans Member 3 (South Africa). We argue that this procedure, which elucidates the degree of hominid-carnivore independence in assemblage formation, will allow researchers to extract for focused analyses high integrity components (hominid and carnivore) from presumably low integrity sites. Comparisons suggest that the hominid- and carnivore-derived components from sites in Olduvai Gorge Bed II (Tanzania), the ST Site Complex at Peninj (Tanzania), and Swartkrans Member 3 formed largely independent of each other, while data from the FLK 22 Zinjanthropus (FLK Zinj) site (Olduvai Gorge Bed I) indicate significant interdependence in assemblage formation. This contrast suggests that some Early Stone Age assemblages (e.g., the Olduvai Gorge Bed II sites, the Peninj ST Site Complex, and Swartkrans Member 3) are probably more useful than others (e.g., FLK Zinj) for assessing the maximal carcass-acquiring abilities of early hominids; in such assemblages as those in the former set, sole hominid-contribution is more confidently discerned and isolated for analysis than in assemblages such as FLK Zinj.     

(40)Ar/(39)Ar dating of Bed I, Olduvai Gorge, Tanzania, and the chronology of early Pleistocene climate change

⁴⁰Ar/³⁹Ar dating of tuffs and lavas of the late Pleistocene volcanic and sedimentary sequence of Olduvai Gorge, north-central Tanzania, provides the basis for a revision of Bed I chronostratigraphy. Bed I extends from immediately above the Naabi Ignimbrite at 2.038 ± 0.005 Ma to Tuff IF at 1.803 ± 0.002 Ma. Tuff IB, a prominent widespread marker tuff in the basin and a key to understanding hominin evolutionary chronologies and paleoclimate histories, has an age of 1.848 ± 0.003 Ma. The largest lake expansion event in the closed Olduvai lake basin during Bed I times encompassed the episode of eruption and emplacement of this tuff. This lake event is nearly coincident with the maximum precessional insolation peak of the entire Bed I/Lower Bed II interval, calculated from an astronomical model of the boreal summer orbital insolation time-series. The succeeding precessional peak also apparently coincides with the next youngest expansion of paleo-Lake Olduvai. The extreme wet/dry climate shifts seen in the upper part of Bed I occur during an Earth-orbital eccentricity maximum, similar to episodic lake expansions documented elsewhere in the East African Rift during the Neogene.     

Long-distance carcass transport at Olduvai Gorge? A quantitative examination of Bed I skeletal element abundances

Relative abundances of skeletal elements at Plio-Pleistocene archaeological sites have long been interpreted to represent selective transport of portions of large prey. Models from optimal foraging theory suggest that the degree of carcass transport selectivity reflects transport constraints, particularly transport distance. A quantitative analysis of skeletal element abundances in five bone assemblages from Bed I, Olduvai Gorge, indicates that within the subset of elements most likely to resist attritional processes, there is no evidence for preferential transport of small or large mammals. The results suggest relatively low carcass transport costs and are most consistent with site formation models favoring short-distance carcass transport. The data are also consistent with the possibility that hominins were not responsible for transporting bones at some sites. Several Bed I assemblages, with the exception of FLK-Zinjanthropus, lack evidence of a functional relationship between flaked stone artifacts and the faunal remains, such as cut-marks or percussion-marks on bone. In conjunction with the skeletal part data, this suggests that hominin involvement with the bone assemblages was minimal at all sites but FLK-Zinjanthropus. The patterning at Bed I contrasts strongly with Middle Stone Age and Middle Paleolithic assemblages, which provide clear evidence for selective transport, suggesting higher transport costs and longer transport distances.     

Soricidae (Mammalia) from the Early Pleistocene of Olduvai Gorge, Tanzania

Soricid remains collected from Bed I of Olduvai Gorge are described. The great majority of the specimens are mandibles. A survey of the mandibles of living African species revealed many differences in characters of the lower teeth and jaw that can be used for identification. On the basis of these characters, nine species are distinguished in the Olduvai collection, of which six are well enough preserved to permit a discussion of their relationships to living species. Three new species and one new subspecies are described. All the Olduvai shrews differ in some respects from their nearest living relatives; three species are close to species from Makapansgat, Swartkrans and Sterkfontein, RSA, though there appear to be slight differences. A change in the soricid fauna takes place within Bed I, interpreted as due to increasing aridity.     

Scavenging or Hunting in Early Hominids: Theoretical Framework and Tests

Evidence from Bed I, Olduvai, supports the hypothesis that scavenging, not hunting, was the major meat-procurement strategy of hominids between 2 and 1.7 million years ago. Data used to evaluate the hunting and scavenging hypotheses are derived from studying cut marks on Bed I bovids, comparing adaptations necessary for scavenging with those of early hominids, and a pa-leoecological reconstruction of Bed I carcass biotnass, carnivore guild, and hominidforaging area.     

A new species of cormorant (Aves: Phalacrocoracidae) from the Pleistocene of Olduvai Gorge,Tanzania

Phalacrocorax owrei nov. sp. is a small cormorant from the Lower Pleistocene of Olduvai Gorge. Osteological proportions are established for the four subgenera of Phalacrocorax, and P. owrei is assigned to the subgenus Stictocarbo. The species was the most abundant bird in the Bed I deposits and is also represented by a few specimens in the middle part of Bed II. Its last known appearance coincides with a change in the local environment when the climate became more arid and the Olduvai Lake became more saline and more alkaline. At other localities in Bed II the extinct P. tanzanice occurs, as well as P. africanus and P. corbo, which breed on the African lakes and seacoast today.     

Plio-Pleistocene synsedimentary fault compartments, foundation for the eastern Olduvai Basin paleoenvironmental mosaic, Tanzania

Normal faults displacing Upper Bed I and Lower Bed II strata of the Plio-Pleistocene Lake Olduvai were studied on the basis of facies and thickness changes as well as diversion of transport directions across them in order to establish criteria for their synsedimentary activity. Decompacted differential thicknesses across faults were then used to calculate average fault slip rates of 0.05-0.47 mm/yr for the Tuff IE/IF interval (Upper Bed I) and 0.01-0.13 mm/yr for the Tuff IF/IIA section (Lower Bed II). Considering fault recurrence intervals of ∼1000 years, fault scarp heights potentially achieved average values of 0.05-0.47 m and a maximum value of 5.4 m during Upper Bed I, which dropped to average values of 0.01-0.13 m and a localized maximum of 0.72 m during Lower Bed II deposition.Synsedimentary faults were of importance to the form and paleoecology of landscapes utilized by early hominins, most traceably and provably Homo habilis as illustrated by the recurrent density and compositional pattern of Oldowan stone artifact assemblage variation across them. Two potential relationship factors are: (1) fault scarp topographies controlled sediment distribution, surface, and subsurface hydrology, and thus vegetation, so that a resulting mosaic of microenvironments and paleoecologies provided a variety of opportunities for omnivorous hominins; and (2) they ensured that the most voluminous and violent pyroclastic flows from the Mt. Olmoti volcano were dammed and conduited away from the Olduvai Basin depocenter, when otherwise a single or set of ignimbrite flows might have filled and devastated the topography that contained the central lake body. In addition, hydraulically active faults may have conduited groundwater, supporting freshwater springs and wetlands and favoring growth of trees.     

The age and stratigraphic position of Olduvai Hominid I

A short history of Olduvai Hominid I is given. On the basis of absolute and relative dating its position in the Naisiusiu Bed, part of the former Bed V, is affirmed. Some connection, on morphological grounds, with other hominids in East Africa is postulated, as well as with cultural material.     

Taphonomic perspectives on hominid site use and foraging strategies during Bed II times at Olduvai Gorge, Tanzania

The faunal assemblages excavated by Mary Leakey in Bed II of Olduvai Gorge, Tanzania, have, like the more well-known Bed I assemblages, traditionally been interpreted as the result of hominid butchering activities in the lake margin and riverine settings of the paleo-Olduvai Basin. A reexamination of all of Leakey's Bed I sites has shown that hominids played little or no role in the formation of all but one of those faunal assemblages, a finding that prompted the reanalysis of the Bed II sites presented here. We expand upon a previous taphonomic study that provided systematic data for HWK East Levels 1–2, MNK Main, and BK. In addition to these assemblages, we provide data on HWK East Levels 3–5, FC West, TK, and SHK. Our data contradict previous interpretations of MNK Main as a hominid accumulation but uphold the contention that BK represents a primarily hominid accumulation reflecting early access to carcasses. The small and poorly preserved assemblages from FC West and TK are difficult to link unambiguously to either hominids or carnivores. Site MNK Main and HWK East Levels 3–5 appear to be death arenas where carcasses accumulated via natural deaths and/or serial predation. Site SHK is severely biased by selective retention and therefore little can be said of its formational history. Nevertheless, no hominid modifications were documented in this assemblage. Comparisons with other Olduvai sites indicate a more conspicuous hyena taphonomic signal during Bed II times than Bed I times, which appears to mirror the changing configuration of the large carnivore guild. These findings also beg the question of what activities were being carried out by hominids with the stone tools discarded at these sites. Although it seems clear that hominids were utilizing stone tools to carry out subsistence activities unrelated to carcass butchery, more excavation and techniques such as phytolith analysis should be employed to explore alternative explanations.     

First occurrence ofXerus cf.inauris (Rodentia,Sciruridae) at Olduvai Bed I (Lower Pleistocene,Tanzania)

PalZ - Some bonodont molars of a ground squirrel are attributed toXerus cf.inauris. Coming from Olduvai Bed I fossiliferous deposits they could represent an intermediate stage between the Laetoli...     

Vegetation during UMBI and deposition of Tuff IF at Olduvai Gorge, Tanzania (ca. 1.8 Ma) based on phytoliths and plant remains

As part of ongoing research at Olduvai Gorge, Tanzania, to determine the detailed paleoenvironmental setting during Bed I and Bed II times and occupation of the basin by early hominins, we present the results of phytolith analyses of Tuff IF which is the uppermost unit of Bed I. Phytoliths were identified in most of the levels and localities on the eastern paleolake margin, but there are not always sufficient numbers of identifiable morphologies to infer the specific type of vegetation due to dissolution. Some surge surfaces and reworked tuff surfaces were vegetated between successive ash falls, as indicated by root-markings and the presence of a variety of phytolith morphotypes. Dicotyledonous wood/bark types were dominant except at the FLK N site just above Tuff IF when monocots are dominant and for the palm-dominated sample from the reworked channel cutting down into Tuff IF at FLK N. The area between the two fault scarps bounding the HWK Compartment, approximately 1 km wide, was vegetated at various time intervals between some of the surges and during the reworking of the Tuff. By lowermost Bed II times the eastern margin was fully vegetated again. Climate and tectonic activity probably controlled the fluctuating lake levels but locally the paleorelief and drainage were probably the controlling factors for the vegetation changes. These data support a scenario of small groups of hominins making brief visits to the paleolake during uppermost Bed I times, followed by a more desirable vegetative environment during lowermost Bed II times.     

The puzzle from JK2—A femur and a tibial fragment (O.H.34) from Olduvai Gorge,Tanzania

During excavations in Bed III, Olduvai Gorge, Tanzania in 1962, a slender fossil femur and part of a tibial shaft were recovered. Their strange appearance resulted in their neglect for many years. Anatomical examination now confirms that these bones are hominid, probably hominine, yet distorted in form. The distortion does not appear to be the result of pathology but due to damage and abrasion while in the deposits; deposits dated at approximately 1 million years B.P. O.H. 34 is the first hominid to be recovered from Bed III, Olduvai Gorge.     

A Homo habilis maxilla and other newly-discovered hominid fossils from Olduvai Gorge, Tanzania

In 1995, a 1.8 million year old hominid maxilla with complete dentition (OH 65) was excavated from Bed I in the western part of Olduvai Gorge. The molar crowns are small relative to the long flaring roots, and the root of the canine is very long and straight. The broad maxilla with wide U-shaped palate and the form of the tooth roots closely match those of KNM-ER 1470 which, in its parietal size and morphology, matches the type specimen of Homo habilis, OH 7. Thus, OH 65 and KNM-ER 1470 group with OH 7 as representatives of H. habilis while some other Olduvai specimens, such as OH 13 and OH 24, have more in common in terms of morphology and brain size with Australopithecus africanus. Between 1995 and 2007, the OLAPP team has recovered teeth of eight other hominid individuals from various parts of Olduvai Gorge. These have been identified as belonging to H. habilis, Paranthropus boisei, and Australopithecus cf. africanus.     

A revised stratigraphic framework for Olduvai Gorge Bed I based on tuff geochemistry

Olduvai Gorge, Tanzania has rich records of Plio-Pleistocene fauna and flora, hominin fossils, and stone artifacts preserved between well-dated tephra layers (tuffs). Accurate correlation between sites in the two million year section is complicated by faulting, erosion, change in physical appearance of the tuffs, and quality of preservation. Traditional tuff geochemical techniques using glass cannot be applied because of poor glass preservation, and previous physical mapping has led to miscorrelations in Bed I. A new approach, using a combination of glass and mineral compositions (feldspar, augite, hornblende, and oxides) produced successful geochemical fingerprints for all ten major Bed I (∼2.03-1.79 Ma) tuffs. These fingerprints make available a reliable means for correlating specific tuffs between the well-dated "Junction" sites, such as FLK and HWK, and less well-dated sites at the basin margins. The new correlations provide a high-resolution stratigraphic framework for Bed I and correct previous miscorrelations in the west of the basin. Olduvai Hominin 65, from western Olduvai, was recovered from a level between Tuff IC and the Ng’eju Tuff, and therefore dates to 1.79-1.84 Ma.     

Variation among early Homo crania from Olduvai Gorge and the Koobi Fora region

Fossils recognized as early Homo were discovered first at Olduvai Gorge in 1959 and 1960. Teeth, skull parts and hand bones representing three individuals were found in Bed I, and more material followed from Bed I and lower Bed II. By 1964, L.S.B. Leakey, P.V. Tobias, and J.R. Napier were ready to name Homo habilis. But almost as soon as they had, there was confusion over the hypodigm of the new species. Tobias himself suggested that OH 13 resembles Homo erectus from Java, and he noted that OH 16 has teeth as large as those of Australopithecus. By the early 1970s, however, Tobias had put these thoughts behind him and returned to the opinion that all of the Olduvai remains are Homo habilis. At about this time, important discoveries began to flow from the Koobi Fora region in Kenya. To most observers, crania such as KNM-ER 1470 confirmed the presence of Homo in East Africa at an early date. Some of the other specimens were problematical. A.C. Walker and R.E. Leakey raised the possibility that larger skulls including KNM-ER 1470 differ significantly from smaller-brained, small-toothed individuals such as KNM-ER 1813. Other workers emphasized that there are differences of shape as well as size among the hominids from Koobi Fora. There is now substantial support for the view that in the Turkana and perhaps also in the Olduvai assemblages, there is more variation than would be expected among male and female conspecifics. One way to approach this question of sorting would be to compare all of the new fossils against the original material from Olduvai which was used to characterize Homo habilis in 1964. A problem is that the Olduvai remains are fragmentary, and none of them provides much information about vault form or facial structure. An alternative is to work first with the better crania, even if these are from other sites. I have elected to treat KNM-ER 1470 and KNM-ER 1813 as key individuals. Comparisons are based on discrete anatomy and measurements. Metric results are displayed with ratio diagrams, by which similarity in proportions for several skulls can be assessed in respect to a single specimen selected as a standard. Crania from Olduvai examined in this way are generally smaller than KNM-ER 1470, although OH 7 has a relatively long parietal. In the Koobi Fora assemblage, there is variation in brow thickness, frontal flattening and parietal shape relative to KNM-ER 1470. These comparisons are instructive, but vault proportions do not help much with the sorting process. Contrasts in the face are much more striking. Measurements treated in ratio diagrams show that both KNM-ER 1813 and OH 24 have relatively short faces with low cheek bones, small orbits and low nasal openings. Also, they display more projection of the midfacial region, just below the nose. This is not readily interpreted to be a female characteristic, since in most hominoid primates the females tend to have flatter lower faces than the males. The obvious size differences among these individuals have usually been interpreted as sex dimorphism, but, in fact, two taxa may be sampled at Olduvai and in the Turkana basin at the beginning of the Pleistocene. One large-brained group made up of KNM-ER 1470, several other Koobi Fora specimens, and probably OH 7, can be called Homo habilis. If these skulls go with femora such as KNM-ER 1481 and the KNM-ER3228 hip, then this species is close in postcranial anatomy to Homo erectus. The other taxon, including small-brained individuals such as KNM-ER 1813 and probably OH 13, seems also to be Homo rather than Australopithecus. If the OH 62 skeleton is part of this assemblage, then the small hominids have postcranial proportions unlike those of Homo erectus. However, it is too early to point unequivocally to one or the other of these groups as the ancestors of later humans. Both differ from Homo erectus in important ways, and both need to be better understood before we can map the earliest history of the Homo clade. © 1993 Wiley-Liss, Inc.     

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.     

Late Pliocene grassland from Olduvai Gorge,Tanzania

The Olduvai fossil plants documented by us in this paper are the first direct evidence for open grassland in the late Neogene of Africa based on macroplant remains. Silicified remains of herbaceous ground cover are exceptionally well preserved in situ within Late Pliocene sediments below the initial pyroclastic ash surge unit of Tuff IF in the uppermost part of Bed I, Olduvai Gorge, northern Tanzania. Published radiometric and palaeomagnetic dates place this grass layer between 1.839 + 0.005 Ma and 1.785 + 0.01 Ma. Exposed at localities on the south side of the Gorge this herbaceous ground cover grew on a floodplain developed on a dried out lake bed, following pronounced lake retreat of saline–alkaline palaeo-Lake Olduvai during a developing dry climatic phase. Sheathed basal culms, rhizomes and roots are interpreted as those of one or more small mat-forming grasses or less likely, sedges. Small dicotyledonous herbs were probably also present. The proximity of adjacent plants indicates a relatively dense ground cover. Roots extended at least 8 cm below the ground surface. Aerial parts of the plants were absent or were not preserved when the weathered basal culms were covered by a thin layer of brown waxy clay, followed by fallout of pyroclastic ash. Both units were mostly eroded away prior to emplacement of a wet, cool pyroclastic surge which then buried and preserved in situ remnants of the herbaceous ground cover. Preservation of the semi-woody rhizomes implies well-drained soils, otherwise the plant material would have quickly rotted. Collections from discontinuous exposures indicate the grassland covered an area of at least a few hectares. This open grassland would have provided grazing for the Late Pliocene fauna.     

Hominid carnivory and foraging strategies, and the socio-economic function of early archaeological sites.

New evidence for the tissue types exploited by early hominids from carcasses possibly acquired through scavenging is derived from the larger mammal bone assemblages from FLK I, level 22 (Zinjanthropus floor), and FLKN levels 1 and 2 from Bed I, Olduvai Gorge, Tanzania. Published skeletal part profiles from the two archaeological sites are evaluated using (i) modern observations on the sequence by which carnivores consume carcass parts in order to assess the timing of hominid access to carcasses, and (ii) measurements of flesh and marrow yields to assess the tissue types sought and acquired. These results suggest that the maximization of marrow (fat) yields, not flesh (protein) yields, was the criterion shaping decisions about carcass processing. Because of evidence for density-dependent destruction of some flesh-bearing parts by scavengers of the hominid-butchered assemblages, however, it is uncertain whether carcass parts were transported and acquired by hominids in a largely defleshed condition. The results on tissue types acquired are combined with a discussion of predation risk, feeding competition and the equipment needs of carcass processing in an attempt to identify archaeological test implications of competing hypotheses for the socio-economic function of the earliest archaeological sites.