Temporal range: 2.1–1.5 Ma
|Lateral view of the KNM ER 1813 cranium (replica), Naturmuseum Senckenberg|
Leakey et al., 1964
The type specimen is OH 7, discovered in 1960 at Olduvai Gorge in Tanzania, associated with the Oldowan lithic industry; the fossils were identified as a separate species of Homo with the proposed binomial name of H. habilis ("handy man") in 1964. In its appearance and morphology, H. habilis is intermediate between Australopithecus and the somewhat younger Homo erectus and its classification in the Homo genus has been the subject of controversial debate since its original proposal. A main argument for its classification as the first Homo ("human") species was its use of flaked stone tools. However, evidence for earlier tool use (3.39 million years ago) by undisputed members of Australopithecus has been found in the 1990s.
Classification as HomoEdit
There has been scholarly debate regarding its placement in the genus Homo rather than the genus Australopithecus. The small size and rather primitive attributes have led some experts (Richard Leakey among them) to propose excluding H. habilis from the genus Homo and placing them instead in Australopithecus as Australopithecus habilis.
Louis Leakey (father of Richard Leakey), the British-Kenyan paleoanthropologist who was the first to suggest the existence of H. habilis, and his wife, Mary Leakey, found the first trace of H. habilis in 1955: two hominin teeth. These were later classified as "milk teeth", and therefore considered difficult to link to taxa, unlike permanent teeth.
H. habilis was short and had disproportionately long arms compared to modern humans; however, it had a less protruding face than the australopithecines from which it is thought to have descended. H. habilis had a cranial capacity slightly less than half of the size of modern humans. Despite the ape-like morphology of the bodies, H. habilis remains are often accompanied by primitive stone tools (e.g. Olduvai Gorge, Tanzania and Lake Turkana, Kenya).
Homo habilis has often been thought to be the ancestor of the more gracile and sophisticated Homo ergaster, which in turn gave rise to the more human-appearing species, Homo erectus. Debates continue over whether all of the known fossils are properly attributed to the species, and some paleoanthropologists regard the taxon as invalid, made up of fossil specimens of Australopithecus and Homo. New findings in 2007 seemed to confirm the view that H. habilis and H. erectus coexisted, representing separate lineages from a common ancestor instead of H. erectus being descended from H. habilis. An alternative explanation would be that any ancestral relationship from H. habilis to H. erectus would have to have been cladogenetic rather than anagenetic (meaning that if an isolated subgroup population of H. habilis became the ancestor of H. erectus, other subgroups remained as unchanged H. habilis until their much later extinction).
Discoveries at Dmanisi, Georgia, which had diverse physical traits and differences in tooth wear, suggest to some scholars that all the contemporary groups of early Homo in Africa, including Homo ergaster, Homo habilis, and Homo rudolfensis are of the same species and should be assigned to Homo erectus, with the implication that variation between these “species” represents the prolonged evolution of one lineage, rather than interspecific differences.
A virtual reconstruction published in 2015 estimated the endocranial volume at between 729 and 824 ml, larger than any previously published value.
H. habilis' brain capacity of around 640 cm³ was on average 50% larger than australopithecines, but considerably smaller than the 1350 to 1450 cm³ range of modern Homo sapiens. These hominins were smaller than modern humans, on average standing no more than 1.3 m (4 ft 3 in) tall.
The body proportions for H. habilis are in accordance with craniodental evidence, suggesting closer association with H. erectus.
Based on dental microwear-texture analysis, Homo habilis (as well as other early Homo-class hominins) likely did not specialize on particularly tough foods. Microwear-texture complexity is, on average, somewhere between that of tough-food feeders and leaf feeders (folivores.) These measurements are analyses of the percentages of tooth surface structure containing "pits" (frequency and depth of dental damage resulting from consumption of certain foods across species). It is a heavily used, and henceforth widely accepted as reliable, measure of wear that a species, on average, endures from eating certain food. These measurements point to an increasingly generalized, and generally omnivorous diet in Homo habilis.
Homo habilis is thought to have mastered the Lower Paleolithic Olduwan tool set, which used stone flakes. H. habilis used these stones to butcher and skin the animals. These stone flakes were more advanced than any tools previously used, and gave H. habilis the edge it needed to prosper in hostile environments previously too formidable for primates. Whether H. habilis was the first hominin to master stone tool technology remains controversial, as Australopithecus garhi, dated to 2.6 million years ago, has been found along with stone tool implements.
Most experts assume the intelligence and social organization of H. habilis were more sophisticated than typical australopithecines or chimpanzees. H. habilis used tools primarily for scavenging, such as cleaving meat off carrion, rather than defense or hunting. Yet, despite tool usage, H. habilis was not the master hunter its sister species (or descendants) proved to be, as ample fossil evidence indicates H. habilis was a staple in the diet of large predatory animals, such as Dinofelis, a large scimitar-toothed predatory cat the size of a jaguar.
Homo habilis coexisted with other Homo-like bipedal primates, such as Paranthropus boisei, some of which prospered for many millennia. However, H. habilis, possibly because of its early tool innovation and a less specialized diet, became the precursor of an entire line of new species, whereas Paranthropus boisei and its robust relatives disappeared from the fossil record. H. habilis may also have coexisted with H. erectus in Africa for a period of 500,000 years.
OH 7 dates to 1.75 million years old, and was discovered by Mary and Louis Leakey on November 4, 1960 at Olduvai Gorge, Tanzania. It is a lower jaw complete with teeth; due to the size of the small teeth, researchers estimate this juvenile individual had a brain volume of 363 cm³. In 1964, found were more than 20 fragments of the left hand. Leakey, paleontologist John Napier, and paleoanthropologist PhillipTobias identified these discoveries as Homo habilis and assisted in classifying OH 7 as the type fossil.
The OH 7 hand of Homo habilis combines traits associated with a precision grip and adaptations related to climbing, which fits well with the semi-long, humanlike hindlimb proportions and a rather chimpanzee-like upper-to-lower arm ratio.
OH 24 (Twiggy) is a roughly deformed cranium about 1.8 million years old discovered in October 1968 at Olduvai Gorge, Tanzania. The brain volume is just under 600 cm³; also, a reduction in the protruding face is present compared to members of more primitive australopithecines.
KNM ER 1813Edit
KNM ER 1813 is a relatively complete cranium, which dates to 1.9 million years old, discovered at Koobi Fora, Kenya by Kamoya Kimeu in 1973. The brain capacity is 510 cm³, not as impressive as other early specimen and forms of H. habilis discovered.
KNM ER 1805Edit
KNM ER 1805 is a specimen of an adult H. habilis made of three pieces of cranium dating to 1.74 million years old from Koobi Fora, Kenya, discovered in 1974. Previous assumptions were that this specimen belongs to H. erectus based on the degree of prognathism and overall cranial shape.
One set of fossil remains (OH 62, for "Olduvai Hominid specimen 62"), discovered by Donald Johanson and Tim White in Olduvai Gorge in 1986, included the important upper and lower limbs, specifically the humerus and femur. Their finding stimulated some debate at the time. Locomotor affinities of OH 62 have been assessed primarily on the basis of its forelimb to hind limb proportions, which are known to be associated with locomotor behavior among living primates. Initial analyses concentrated on comparisons to the Australopithecus afarensis A.L. 288-1 ("Lucy"). In most dimensions—measured or estimated—the OH 62 upper limb remains equaled or exceeded those of A.L. 288-1, while its lower limb remains (principally the femur) appeared to be smaller. In particular, using a length estimate for the humerus of 264 mm, and a length estimate for the less complete femur of ‘‘no greater than that of A.L. 288-1 (280 mm),'' a possible humerofemoral length index is close to 95%, which is more like that of modern chimpanzees (averaging about 1.00) than modern humans (averaging about 0.72). In this sense, it was more ‘‘primitive'' than A.L. 288-1, with a length index of 0.85.
LD 350-1 is a fossil jawbone fragment discovered in 2013, which has been dated to 2.8 million years ago and argued to be intermediate between Australopithecus and H. habilis. The fossil was claimed as the earliest evidence of the genus Homo known to date. The individual in question lived just after a major climate shift in the region, when forests and waterways were rapidly replaced by arid savannah.
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