A new species of the genusHomo (primates: Hominidae) from the Plio/Pleistocene of Koobi Fora,in Kenya

Reassessment of the hominine cranium, KNM-ER 1813, from the Plio/Pleistocene of Koobi Fora, in Kenya, shows that it is not a small-brained, extreme female variant ofH. habilis Leakey, Tobias, & Napier, 1964. Its cranial and dental morphology, morphometrics, and proportions do not conform with eitherH. habilis orH. antiquus Ferguson, 1984. On the basis of its distinctive morphological pattern and mensural gaps which distinguish it fromH. habilis andH. antiquus, the cranium KNM-ER 1813 is described as a common variant representing a male of a small-brained, intermediate population linkingH. habilis 1.83 Myr BP withH. antiquus 2.9 Myr BP, and a new paleospecies of the genusHomo. A key to the Homininae is provided and the phylogenetic relationship of KNM-ER 1813 toH. habilis andH. antiquus is discussed. This paper is dedicated to the memory of my wife,Grace, whose assistance will be sorely missed.     

A new species of the genusAustralopithecus (primates: hominidae) from Plio/Pleistocene deposits west of Lake Turkana in Kenya

The cranium of a robust australopithecine, KNM WT 17000, was discovered from the Plio/Pleistocene deposits west of Lake Turkana in Kenya, and assigned to the speciesAustralopithecus boisei Leakey, 1959. A comparative morphological study shows that it does not conform with the diagnosis forA. boisei. It is characterized by having a much smaller brain, a low hyperprognathous facial skeleton, and a less developed masticatory apparatus. Its unique morphological pattern justifies its placement in a new taxon which is calledAustralopithecus walkeri n. sp.     

Taxonomic status of the hominine cranium KNM-ER 1813 (primates: Homininae) from the Plio/Pleistocene of Koobi Fora

The hominine cranium KNM-ER 1813, from the late Plio/Pleistocene of Koobi Fora, has been regarded recently by some authors as a female ofHomo habilis Leakey, Tobias, andNapier, 1964 and by others as an enigma. Reassessment of its cranial morphology, dental metrics, proportions, and a new detailed determination of its sex indicates that it does not conform with the diagnosis forH. habilis, and is probably a male. It is sympatric withH. habilis yet shows more primitive features and rather a closer affinity to the smaller, more primitive chronospeciesH. antiquus Ferguson, 1984, and is thus the first, nearly complete skull of our oldest known human ancestor.     

Ar/Ar dating, paleomagnetism, and tephrochemistry of Pliocene strata of the hominid-bearing Woranso-Mille area, west-central Afar Rift, Ethiopia

⁴⁰Ar/³⁹Ar dating of tuffs and mafic lavas, tephra geochemistry, and paleomagnetic reversal stratigraphy have been used to establish the chronostratigraphy of the Pliocene hominid-bearing fossiliferous succession at Woranso-Mille, a paleontological study area in the western part of the central Afar region of Ethiopia. The succession in the northwestern part of the study area ranges in ⁴⁰Ar/³⁹Ar age from 3.82-3.570 Ma, encompassed by paleomagnetic subchron C2Ar (4.187-3.596 Ma). One of the major tuff units, locally named the Kilaytoli tuff, is correlative on the basis of age and geochemistry to the Lokochot Tuff of the Turkana Basin. A hominid partial skeleton (KSD-VP-1) was found in strata whose precise stratigraphic position and age is still under investigation, but is believed to correspond to the later part of this interval. Woranso-Mille fills a significant gap in the fossil record of northeastern Africa at the time of the lower to middle Pliocene transition, when many extant species lineages of African fauna were established.     

Length estimate for KNM-ER 736, a hominid femur from the lower pleistocene of East Africa

Our knowledge concerning stature in earlyHomo is scanty. In this paper, based on comparison with the fossil femur KNM-ER 999, an estimate of 482 mm femur length is derived for KNM-ER 736, the latter dating from the Lower Pleistocene. From comparison with other fossil and modern femora, KNM-ER 736 appears to be the longest hominid femur so far recovered from a site of Early Pleistocene age. Moreover, the estimated femur length is higher than the published mean values of most modern populations. Provided that trunk and head proportions were not radically different from modernH. sapiens, the finding would suggest that a stature similar to that of modern man was already reached by East AfricanHomo as early as about 1.6 Myr before present.     

Reassessment of the paleoenvironment and preservation of hominid fossils from Hadar, Ethiopia.

Samples of paleosols from locality AL-333, known for numerous specimens of Australopithecus afarensis, were analyzed in order to reconstruct the original soils and environment of burial of the associated fossil hominids. The bones were found in swale-like features, within the calcareous and coarse-grained basal portion of a paleosol. This is more like an assemblage of bones buried during a single depositional episode, such as a flood, than an assemblage accumulated on a soil over a long period of time by carnivores or other means of death. What killed the hominids remains unclear, but considering the association of originally disarticulated bones of such hydraulically distinct types as phalanges and maxillae, it is very likely that they died and partially rotted at or very near this site. The paleosols at AL-333, here named the Fo and Go clay paleosols, have calcareous rhizoconcretions, granular surface horizons, prismatic peds, and shallow calcareous nodules and stringers like soils now supporting grassy woodland in semiarid regions. Although this group of hominids was buried in streamside gallery woodland, there is evidence from Laetoli, Tanzania, that A. afarensis ventured out into open wooded grassland as well. Evidence for this should be sought from other paleosols at Hadar.     

Morphology of the Pliocene partial hominid skeleton (A.L. 288-1) from the Hadar formation,Ethiopia

The upper part of the Pliocene Hadar Formation, central Afar, Ethiopia, has yielded a 40% complete fossil hominid skeleton (A.L. 288-1, “Lucy”). This specimen is described in detail and selected measurements and illustrations are provided.     

Evolution of Hominid Femur and Tibia: A morphometric approach to the evolutionary research in anthropology

Some theoretical and methodological morphometrical approaches in evolutionary anthropology and paleoanthropology are reviewed in this study. It is shown which are the contemporary possibilities of sophisticated biometrical and biostatistical methods and the role of the morphometrical approach. A new approach, experimental morphometrics, is presented, reflecting recent trends in evolutionary morphology as well as sophisticated biostatistical methods. The approach emphasizes the complex inter-related approach to the data processing and a double nature of morphometric data, i.e. biological and biostatistical one. The practical use of experimental morphometry is given for the two examples of analyses of the evolution of the hominoid and hominid femur and tibia. The hypothesis on a two stage restructuring of morphology of the hominid femur and tibia is supported by experimental results. Two different steps during this restructuring could be recognized: 1) Structural remodelling typical for the origin of hominids and australopithecine evolution, and 2) proportional remodelling of lower limb long bones which is connected with the Australopithecus/Homo transition (i.e. mainly Homo habilis stage). The results confirm the increasing trend of bipedal adaptations on the early hominid lower limb skeleton. Analysis of microevolutionary trends on the Homo sapiens femur and tibia indicates at least three different morphological patterns, Paleolithic, Neolithic and Recent, with numerous specific features in morphology and proportions. Neanderthal morphology is very derived. Upper Paleolithic/Mesolithic/Neolithic transition has a key character for the understanding of post-Paleolithic morphology. A very high sexual dimorphism of the femur and tibia has been demonstrated for Upper Paleolithic and Neolithic populations. Presented at the Foundation of Different Approaches to the Study of Human Evolution edited by B. Sigmon & V.V. Leonovicova-Liblice, September 1–3, 1989     

Phylogeny of early Australopithecus: new fossil evidence from the Woranso-Mille (central Afar,Ethiopia)

The earliest evidence of Australopithecus goes back to ca 4.2 Ma with the first recorded appearance of Australopithecus ‘anamensis’ at Kanapoi, Kenya. Australopithecus afarensis is well documented between 3.6 and 3.0 Ma mainly from deposits at Laetoli (Tanzania) and Hadar (Ethiopia). The phylogenetic relationship of these two ‘species’ is hypothesized as ancestor–descendant. However, the lack of fossil evidence from the time between 3.6 and 3.9 Ma has been one of its weakest points. Recent fieldwork in the Woranso-Mille study area in the Afar region of Ethiopia has yielded fossil hominids dated between 3.6 and 3.8 Ma. These new fossils play a significant role in testing the proposed relationship between Au. anamensis and Au. afarensis. The Woranso-Mille hominids (3.6–3.8 Ma) show a mosaic of primitive, predominantly Au. anamensis-like, and some derived (Au. afarensis-like) dentognathic features. Furthermore, they show that, as currently known, there are no discrete and functionally significant anatomical differences between Au. anamensis and Au. afarensis. Based on the currently available evidence, it appears that there is no compelling evidence to falsify the hypothesis of ‘chronospecies pair’ or ancestor–descendant relationship between Au. anamensis and Au. afarensis. Most importantly, however, the temporally and morphologically intermediate Woranso-Mille hominids indicate that the species names Au. afarensis and Au. anamensis do not refer to two real species, but rather to earlier and later representatives of a single phyletically evolving lineage. However, if retaining these two names is necessary for communication purposes, the Woranso-Mille hominids are best referred to as Au. anamensis based on new dentognathic evidence.     

Reappraisal of the taxonomic status of the cranium Stw 53 from the Plio/Pleistocene of Sterkfontein,in South Africa

A fossil skull, Stw 53, from the Plio/Pleistocene of Sterkfontein, in South Africa, has been referred toHomo habilis Leakey, Napier, andTobias, 1964. Reappraisal of its putative hominine affinity reveals a closer resemblance toAustralopithecus africanus Dart, 1925. The skull, as reconstructed, is too small forH. habilis; with no indication of brain expansion overA. africanus; has a facial angle outside the hominine range, but identical with that ofA. africanus; and whose teeth are not elongated but display buccolingual expansion. Although it was found in the same strata (Member 5) as stone tools, there is no causal connection. It has been dated faunistically at 2–1.5 my BP, but due to an unconformity it is suggested that it could be older. In spite of its late date, Stw 53 shows no intermediate characters which could support a trend towardsH. habilis orA. robustus Broom, 1938. It may, therefore, represent a relict population ofA. africanus.     

Taxonomic status of the hominid mandible KNM-ER TI 13150 from the middle pliocene of tabarin,in Kenya

A partial mandible with two molars intact was recovered between 1981 and 1984 from deposits of the Middle Pliocene at Tabarin, in Kenya. It has been described and assigned toAustralopithecus cf.afarensis Johanson, White, andCoppens, 1978, with the condition that if ‘A. afarensis’ is revised, then the attribution may change. The taxon ‘A. afarensis’ was found to be invalid and was revised. The smaller specimens of ‘A. afarensis,’ to which the Tabarin mandible was said to be similar, were redescribed asHomo antiquus Ferguson, 1984. Since the Tabarin mandible andH. antiquus are successive transients of the same gens and are allopatric, the Tabarin hominid population is described as an earlier chronosubspecies,Homo antiquus praegens ssp. n.     

Inventory of remains of Hominidae from Pliocene-Pleistocene formations of the lower Omo basin, Ethiopia (1967-1972)

Since its initiation in 1966 the Omo Research Expedition has recovered a series of hominid fossils, in association with many vertebrate taxa, from formations of Pliocene/Pleistocene age from the lower Omo basin, southern Ethiopia. These fossiliferous formations span a time range from over 4.2 m.y. to about 1.4 m. y. on the basis of K/A age determination. Hominid remains have been found so far to occur at two localities in the upper part of the Usno Formation (～ 2.9 m.y.) and in the Shungura Formation at 79 localities from successive Members B through levels postdating J, a time span between 3 m.y. and 1.4 m.y. The remains—inventoried here according to skeletal part, locality and stratigraphic level, age and situation—include numerous isolated and associated teeth, mandibles, partial maxillae, portions of crania, and elements of the postcranial skeleton.     

Current status of wilt/root rot diseases in major chickpea growing areas of Ethiopia

Wilt/root rot diseases are a major chickpea production constraint in Ethiopia causing yield losses by reducing the number of plants. To determine the current status of disease incidence and distribution, surveys were conducted in the 2013/2014 and 2014/2015 cropping seasons in major chickpea growing zones of Ethiopia. Despite recent efforts in dissemination of improved varieties, low to high incidence of 0.0–83.4, 0.0–27.6, 1.3–19.8 and 0.0–16.3% and 1.0–81.9, 0.0–25.5, 3.0–13.9 and 1.0–21.5% in East Gojjam, Southwest Shewa, North Shewa and West Shewa in 2013/2014 and 2014/2015, respectively. Therefore, integrated pest management strategies should be developed and availed to farmers.     

Geometric morphometric analysis of the crown morphology of the lower first premolar of hominins, with special attention to Pleistocene Homo

This article is the third of a series that explores hominin dental crown morphology by means of geometric morphometrics. After the analysis of the lower second premolar and the upper first molar crown shapes, we apply the same technique to lower first premolar morphology. Our results show a clear distinction between the morphology seen in earlier hominin taxa such as Australopithecus and African early Homo, as well as Asian H. erectus, and more recent groups such as European H. heidelbergensis, H. neanderthalensis, and H. sapiens. The morphology of the earlier hominins includes an asymmetrical outline, a conspicuous talonid, and an occlusal polygon that tends to be large. The morphology of the recent hominins includes a symmetrical outline and a reduced or absent talonid. Within this later group, premolars belonging to H. heidelbergensis and H. neanderthalensis tend to possess a small and mesiolingually-displaced occlusal polygon, whereas H. sapiens specimens usually present expanded and centered occlusal polygons in an almost circular outline. The morphological differences among Paranthropus, Australopithecus, and African early Homo as studied here are small and evolutionarily less significant compared to the differences between the earlier and later homin taxa. In contrast to the lower second premolar and the upper first molar crown, the inclusion of a larger hominin sample of lower first premolars reveals a large allometric component.     

New discoveries of Gigantopithecus blacki teeth from Chuifeng Cave in the Bubing Basin, Guangxi, south China

Ninety two Gigantopithecus blacki teeth have recently been recovered in situ at Chuifeng Cave in the Bubing Basin, Guangxi, south China. The hominoid teeth are associated with a typical early Pleistocene fauna. In comparison with Gigantopithecus of known provenience, for which classification is problematic, the Chuifeng sample can be allocated definitively to G. blacki. The new collection represents the largest sample of this species known, with the exception of the material from Liucheng. Statistical analysis of the mammal fauna indicates that G. blacki is one of the dominant elements, comprising 9% of the fauna. Eleven teeth (12% of the sample) of G. blacki are diagnosed as having caries. In addition, wear on M₃ shows that G. blacki was adapted to consume tough or fibrous food and this wear may potentially imply relative longevity. Further study of this large sample of Gigantopithecus will provide additional insight into the paleobiology of this extinct hominoid.     

Cutmarked bones from Pliocene archaeological sites at Gona, Afar, Ethiopia: implications for the function of the world's oldest stone tools

Newly recorded archaeological sites at Gona (Afar, Ethiopia) preserve both stone tools and faunal remains. These sites have also yielded the largest sample of cutmarked bones known from the time interval 2.58-2.1 million years ago (Ma). Most of the cutmarks on the Gona fauna possess obvious macroscopic (e.g., deep V-shaped cross-sections) and microscopic (e.g., internal microstriations, Herzian cones, shoulder effects) features that allow us to identify them confidently as instances of stone tool-imparted damage caused by hominid butchery. In addition, preliminary observations of the anatomical placement of cutmarks on several of the recovered bone specimens suggest that Gona hominids may have eviscerated carcasses and defleshed the fully muscled upper and intermediate limb bones of ungulates--activities that further suggest that Late Pliocene hominids may have gained early access to large mammal carcasses. These observations support the hypothesis that the earliest stone artifacts functioned primarily as butchery tools and also imply that hunting and/or aggressive scavenging of large ungulate carcasses may have been part of the behavioral repertoire of hominids by c. 2.5 Ma, although a larger sample of cutmarked bone specimens is necessary to support the latter inference.     

A new species of Golunda (Rodentia, Muridae) from the Late Pleistocene of Indian Himalaya

The youngest fossil Golunda (Rodentia, Muridae) is described from the Late Pleistocene fluvio-lacustrine deposits, exposed at Dulam (Bageshwar), Kumaun Lesser Himalaya, India. The age of fossiliferrous horizon is estimated as 31,000 yr BP. A new species, Golunda dulamensis nov. sp. has highly derived characters, e.g., antero-posteriorly stretched molars, upper molars with more length and less width, stephanodonty, cusps in M₃ strongly inclined backward giving the molars a very stretched aspect, and metaconid and entoconid in M₃ forming almost straight lingual row of the cusps. G. dulamensis nov. sp. is most similar to present day G. ellioti but differs from the later slightly by larger size, a thin connection between t₄ and t₅ in M¹, and comparatively larger entoconid and very weakly developed antero-labial cusp in M₃. We suggest that highly specialized molars of G. dulamensis nov. sp. and present day G. ellioti are derivable through G. kelleri. We also propose that Golunda migrated from Asia to Africa, not from Africa to Asia as was thought by earlier workers.     

Paleoreconstruction of Pleistocene environments of human habitats in the Late Pleistocene and Holocene near the Charyshskii Naves cave, Central Altai, Russia

The results of the study of the small mammal fauna from the Charyshskii Naves cave (Central Altai, Russia) in the 2003 field season are provided. The dynamics of fossil small mammals was studied and the natural habitats of the ancient man were reconstructed on this basis. Two stages of sedimentation, corresponding to the domination of different biotopes, were recognized.