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Paranthropus aethiopicus Temporal range: Pliocene-Pleistocene, | |
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Reconstruction of KNM WT 17000 | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Mammalia |
Order: | Primates |
Suborder: | Haplorhini |
Infraorder: | Simiiformes |
Family: | Hominidae |
Subfamily: | Homininae |
Tribe: | Hominini |
Genus: | † Paranthropus |
Species: | †P. aethiopicus |
Binomial name | |
†Paranthropus aethiopicus | |
Synonyms | |
Paranthropus aethiopicus is an extinct species of robust australopithecine from the Late Pliocene to Early Pleistocene of East Africa about 2.7–2.3 million years ago. However, it is much debated whether or not Paranthropus is an invalid grouping and is synonymous with Australopithecus , so the species is also often classified as Australopithecus aethiopicus. [1] Whatever the case, it is considered to have been the ancestor of the much more robust P. boisei . It is debated if P. aethiopicus should be subsumed under P. boisei, and the terms P. boisei sensu lato ("in the broad sense") and P. boisei sensu stricto ("in the strict sense") can be used to respectively include and exclude P. aethiopicus from P. boisei.
Like other Paranthropus, P. aethiopicus had a tall face, thick palate, and especially enlarged cheek teeth. However, likely due to its archaicness, it also diverges from other Paranthropus, with some aspects resembling the much earlier A. afarensis . P. aethiopicus is known primarily by the skull KNM WT 17000 from West Lake Turkana, Kenya, as well as some jawbones from Koobi Fora; the Shungura Formation, Ethiopia; and Laetoli, Tanzania. These locations featured bushland to open woodland landscapes with edaphic (water-logged) grasslands.
In 1968, French palaeontologist Camille Arambourg and Breton anthropologist Yves Coppens described "Paraustralopithecus aethiopicus" based on a toothless mandible (Omo 18) from the Shungura Formation, Ethiopia. The name aethiopicus refers to Ethiopia. [2] In 1976, American anthropologist Francis Clark Howell and Coppens reclassified it as A. africanus. [3]
In 1985, the skull KNM WT 17000 dating to 2.5 million years ago was reported from Koobi Fora, Lake Turkana, Kenya, by anthropologists Alan Walker and Richard Leakey. A partial jawbone from a different individual, KNM-WT 16005, was also discovered. They clearly belonged to a robust australopithecine. [4] By this point in time, much younger robust australopithecines had been reported from South Africa ( robustus ) and East Africa ( boisei ), and been variously assigned to either Australopithecus or a unique genus Paranthropus . [5] Walker and Leakey assigned KNM WT 17000 to the boisei clade. They noted several anatomical differences, but were unsure if this stemmed from the specimens' archaicness or represented the normal range of variation for the species. If the former, they recommended classifying them and similar specimens into a different species, aethiopicus (and recommended that Paraustralopithecus be invalid). The discovery of these archaic specimens overturned previous postulations that P. robustus was the ancestor of the much more robust P. boisei (a hypothesis notably argued by palaeoanthropologist Yoel Rak in 1985) by establishing the boisei lineage as beginning long before robustus had existed. [4]
In 1989, palaeoartist Walter Ferguson recommended KNM WT 17000 be classified into a different species, walkeri, because the holotype of aethiopicus comprised only the jawbone and KNM WT 17000 preserves no jaw elements. [3] Ferguson's classification is almost universally ignored, [6] and is considered to be synonymous with P. aethiopicus. [7]
Several more lower and upper jaw specimens have been unearthed in the Shungura Formation, [5] : 112–113 including a juvenile specimen, L338y-6. [8] In 2002, a 2.7–2.5 Ma maxilla, EP 1500, from Laetoli, Tanzania, was assigned to P. aethiopicus. Also found was the upper portion of a tibia, but it cannot definitively be associated with EP 1500 and thus with P. aethiopicus. [9]
The genus Paranthropus (from Ancient Greek παρα para beside or alongside, and άνθρωπος ánthropos man, [10] otherwise known as "robust australopithecines") typically includes P. aethiopicus, P. boisei, and P. robustus. P. aethiopicus is the earliest member of the genus, with the oldest remains, from the Ethiopian Omo Kibish Formation, dated to 2.6 million years ago (mya) at the end of the Pliocene. [11] It is possible that P. aethiopicus evolved even earlier, up to 3.3 mya, on the expansive Kenyan floodplains of the time. [12] P. aethiopicus is only confidently identified from the skull KNM WT 17000 and a few jaws and isolated teeth, and is generally considered to have been ancestral to P. boisei which also inhabited East Africa, making it a chronospecies. Because of this relationship, it is debatable if P. aethiopicus should be subsumed under P. boisei or if the differences stemming from archaicness should justify species distinction. The terms P. boisei sensu lato ("in the broad sense") and P. boisei sensu stricto ("in the strict sense") can be used to respectively include and exclude P. aethiopicus from P. boisei when discussing the lineage as a whole. [5] : 106–107
It is also debated if Paranthropus is a valid natural grouping (monophyletic) or an invalid grouping of similar-looking hominins (paraphyletic). Because skeletal elements are so limited in these species, their affinities with each other and to other australopithecines is difficult to gauge with accuracy. The jaws are the main argument for monophyly, but such anatomy is strongly influenced by diet and environment, and could in all likelihood have evolved independently in P. boisei and P. robustus. Proponents of monophyly consider P. aethiopicus to be ancestral to the other two species, or closely related to the ancestor. Proponents of paraphyly allocate these three species to the genus Australopithecus as A. boisei, A. aethiopicus, and A. robustus. British geologist Bernard Wood and American palaeoanthropologist William Kimbel are major proponents of monophyly, and against include Walker. [5] : 117–121
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This species, originally named Paraustralopithecus aethiopicus, cannot retain the species epithet aethiopicus if moved to genus Australopithecus because Australopithecus aethiopicus is already a junior synonym of Australopithecus afarensis . Such a classification would have to use the name Australopithecus walkeri for this species. The change of species epithet would also happen in a taxonomy that classifies all hominins as Homo. [14]
Typical of Paranthropus, KNM WT 17000 is heavily built, and the palate and base of the skull are about the same size as the P. boisei holotype OH 5. The brain volume of KNM WT 17000 was estimated to have been 410 cc (25 cu in), which is smaller than that of other Paranthropus. The combination of a tall face, thick palate, and small braincase caused a highly defined sagittal crest on the midline of the skull. The only complete tooth crown of the specimen is the right third premolar, whose dimensions are well above the range of variation for P. robustus and on the upper end for P. boisei. Unlike other Paranthropus, KNM WT 17000 did not have a flat face, and the jaw jutted out (prognathism). In regard to the temporal bone, KNM WT 17000 differs from other Paranthropus in that the squamous part of temporal bone is extensively pneumaticised, the tympanic part of the temporal bone is not as vertically orientated, the base of the skull is weakly flexed, the postglenoid process is completely anterior to (in front of) the tympanic, the tympanic is somewhat tubular, and the articular tubercle is weak. Like P. boisei, the foramen magnum where the skull connects to the spine is heart-shaped. [4] The temporalis muscle was probably not directed as forward as it was in P. boisei, meaning the P. aethiopicus jaw likely processed food with the incisors before using the cheek teeth. The incisors of P. boisei are thought to have not been involved in processing food. The long distance between the first molar and the jaw hinge would suggest KNM WT 17000 had an exceptionally long ramus of the mandible (connecting the lower jaw to the skull), though the hinge's location indicates the ramus would not have been particularly deep (it would have been weaker). This may have produced a less effective bite compared to P. boisei. [8]
KNM-WT 16005 is quite similar to the Peninj Mandible assigned to P. boisei, exhibiting postcanine megadontia with relatively small incisors and canines (based on the tooth roots) and large cheek teeth. [4] Nonetheless, the incisors were likely much broader in KNM-WT 16005. [8] KNM-WT 16005 preserved four cheek teeth on the left side: the third premolar measuring 10.7 mm × 13.8 mm (0.42 in × 0.54 in), the fourth premolar measuring 12 mm × 15 mm (0.47 in × 0.59 in), the first molar measuring 15.7 mm × 14.3 mm (0.62 in × 0.56 in), and the second molar measuring 17 mm × 16.7 mm (0.67 in × 0.66 in). The fourth premolar and first molar are a little smaller than those of the Peninj mandible, and the second molar a bit bigger. The KNM-WT 16005 jawbone is smaller than what KNM WT 17000 would have had. [4]
Many of these P. aethiopicus features are shared with the early A. afarensis , further reiterating the species' archaicness. [4] [8]
In general, Paranthropus are thought to have been generalist feeders, with the heavily built skull becoming important when chewing less desirable, lower quality foods in times of famine. Unlike P. boisei which generally is found in the context of closed, wet environments, P. aethiopicus seems to have inhabited bushland to open woodland habitats around edaphic (water-logged) grasslands. [5] : 121 Around 2.5 million years ago, at the Pliocene/Pleistocene border, the Omo–Turkana Basin featured a mix of forests, woodlands, grasslands, and bushlands, though grasslands appear to have been expanding through the Early Pleistocene. Homo seems to have entered the region 2.5–2.4 million years ago. [15]
Homo habilis is an extinct species of archaic human from the Early Pleistocene of East and South Africa about 2.3 million years ago to 1.65 million years ago (mya). Upon species description in 1964, H. habilis was highly contested, with many researchers recommending it be synonymised with Australopithecus africanus, the only other early hominin known at the time, but H. habilis received more recognition as time went on and more relevant discoveries were made. By the 1980s, H. habilis was proposed to have been a human ancestor, directly evolving into Homo erectus, which directly led to modern humans. This viewpoint is now debated. Several specimens with insecure species identification were assigned to H. habilis, leading to arguments for splitting, namely into "H. rudolfensis" and "H. gautengensis" of which only the former has received wide support.
Kenyanthropus is a genus of extinct hominin identified from the Lomekwi site by Lake Turkana, Kenya, dated to 3.3 to 3.2 million years ago during the Middle Pliocene. It contains one species, K. platyops, but may also include the 2 million year old Homo rudolfensis, or K. rudolfensis. Before its naming in 2001, Australopithecus afarensis was widely regarded as the only australopithecine to exist during the Middle Pliocene, but Kenyanthropus evinces a greater diversity than once acknowledged. Kenyanthropus is most recognisable by an unusually flat face and small teeth for such an early hominin, with values on the extremes or beyond the range of variation for australopithecines in regard to these features. Multiple australopithecine species may have coexisted by foraging for different food items, which may be reason why these apes anatomically differ in features related to chewing.
Paranthropus is a genus of extinct hominin which contains two widely accepted species: P. robustus and P. boisei. However, the validity of Paranthropus is contested, and it is sometimes considered to be synonymous with Australopithecus. They are also referred to as the robust australopithecines. They lived between approximately 2.9 and 1.2 million years ago (mya) from the end of the Pliocene to the Middle Pleistocene.
Australopithecus (, OS-trə-lə-PITH-i-kəs, -loh-; or is a genus of early hominins that existed in Africa during the Pliocene and Early Pleistocene. The genera Homo, Paranthropus, and Kenyanthropus evolved from some Australopithecus species. Australopithecus is a member of the subtribe Australopithecina, which sometimes also includes Ardipithecus, though the term "australopithecine" is sometimes used to refer only to members of Australopithecus. Species include A. garhi, A. africanus, A. sediba, A. afarensis, A. anamensis, A. bahrelghazali and A. deyiremeda. Debate exists as to whether some Australopithecus species should be reclassified into new genera, or if Paranthropus and Kenyanthropus are synonymous with Australopithecus, in part because of the taxonomic inconsistency.
Homo ergaster is an extinct species or subspecies of archaic humans who lived in Africa in the Early Pleistocene. Whether H. ergaster constitutes a species of its own or should be subsumed into H. erectus is an ongoing and unresolved dispute within palaeoanthropology. Proponents of synonymisation typically designate H. ergaster as "African Homo erectus" or "Homo erectus ergaster". The name Homo ergaster roughly translates to "working man", a reference to the more advanced tools used by the species in comparison to those of their ancestors. The fossil range of H. ergaster mainly covers the period of 1.7 to 1.4 million years ago, though a broader time range is possible. Though fossils are known from across East and Southern Africa, most H. ergaster fossils have been found along the shores of Lake Turkana in Kenya. There are later African fossils, some younger than 1 million years ago, that indicate long-term anatomical continuity, though it is unclear if they can be formally regarded as H. ergaster specimens. As a chronospecies, H. ergaster may have persisted to as late as 600,000 years ago, when new lineages of Homo arose in Africa.
Homo rudolfensis is an extinct species of archaic human from the Early Pleistocene of East Africa about 2 million years ago (mya). Because H. rudolfensis coexisted with several other hominins, it is debated what specimens can be confidently assigned to this species beyond the lectotype skull KNM-ER 1470 and other partial skull aspects. No bodily remains are definitively assigned to H. rudolfensis. Consequently, both its generic classification and validity are debated without any wide consensus, with some recommending the species to actually belong to the genus Australopithecus as A. rudolfensis or Kenyanthropus as K. rudolfensis, or that it is synonymous with the contemporaneous and anatomically similar H. habilis.
Paleoanthropology or paleo-anthropology is a branch of paleontology and anthropology which seeks to understand the early development of anatomically modern humans, a process known as hominization, through the reconstruction of evolutionary kinship lines within the family Hominidae, working from biological evidence and cultural evidence.
Australopithecus africanus is an extinct species of australopithecine which lived between about 3.3 and 2.1 million years ago in the Late Pliocene to Early Pleistocene of South Africa. The species has been recovered from Taung, Sterkfontein, Makapansgat, and Gladysvale. The first specimen, the Taung child, was described by anatomist Raymond Dart in 1924, and was the first early hominin found. However, its closer relations to humans than to other apes would not become widely accepted until the middle of the century because most had believed humans evolved outside of Africa. It is unclear how A. africanus relates to other hominins, being variously placed as ancestral to Homo and Paranthropus, to just Paranthropus, or to just P. robustus. The specimen "Little Foot" is the most completely preserved early hominin, with 90% of the skeleton intact, and the oldest South African australopith. However, it is controversially suggested that it and similar specimens be split off into "A. prometheus".
Australopithecus anamensis is a hominin species that lived approximately between 4.3 and 3.8 million years ago and is the oldest known Australopithecus species, living during the Plio-Pleistocene era.
A sagittal crest is a ridge of bone running lengthwise along the midline of the top of the skull of many mammalian and reptilian skulls, among others. The presence of this ridge of bone indicates that there are exceptionally strong jaw muscles. The sagittal crest serves primarily for attachment of the temporalis muscle, which is one of the main chewing muscles. Development of the sagittal crest is thought to be connected to the development of this muscle. A sagittal crest usually develops during the juvenile stage of an animal in conjunction with the growth of the temporalis muscle, as a result of convergence and gradual heightening of the temporal lines.
Australopithecus garhi is a species of australopithecine from the Bouri Formation in the Afar Region of Ethiopia 2.6–2.5 million years ago (mya) during the Early Pleistocene. The first remains were described in 1999 based on several skeletal elements uncovered in the three years preceding. A. garhi was originally considered to have been a direct ancestor to Homo and the human line, but is now thought to have been an offshoot. Like other australopithecines, A. garhi had a brain volume of 450 cc (27 cu in); a jaw which jutted out (prognathism); relatively large molars and premolars; adaptations for both walking on two legs (bipedalism) and grasping while climbing (arboreality); and it is possible that, though unclear if, males were larger than females. One individual, presumed female based on size, may have been 140 cm tall.
Paranthropus robustus is a species of robust australopithecine from the Early and possibly Middle Pleistocene of the Cradle of Humankind, South Africa, about 2.27 to 0.87 million years ago. It has been identified in Kromdraai, Swartkrans, Sterkfontein, Gondolin, Cooper's, and Drimolen Caves. Discovered in 1938, it was among the first early hominins described, and became the type species for the genus Paranthropus. However, it has been argued by some that Paranthropus is an invalid grouping and synonymous with Australopithecus, so the species is also often classified as Australopithecus robustus.
Paranthropus boisei is a species of australopithecine from the Early Pleistocene of East Africa about 2.5 to 1.15 million years ago. The holotype specimen, OH 5, was discovered by palaeoanthropologist Mary Leakey in 1959 at Olduvai Gorge, Tanzania and described by her husband Louis a month later. It was originally placed into its own genus as "Zinjanthropus boisei", but is now relegated to Paranthropus along with other robust australopithecines. However, it is also argued that Paranthropus is an invalid grouping and synonymous with Australopithecus, so the species is also often classified as Australopithecus boisei.
The australopithecines, formally Australopithecina or Hominina, are generally any species in the related genera of Australopithecus and Paranthropus. It may also include members of Kenyanthropus, Ardipithecus, and Praeanthropus. The term comes from a former classification as members of a distinct subfamily, the Australopithecinae. They are now classified within the Australopithecina subtribe of the Hominini tribe. All these related species are now sometimes collectively termed australopithecines, australopiths or homininans. They are the extinct, close relatives of modern humans and, together with the extant genus Homo, comprise the human clade. Members of the human clade, i.e. the Hominini after the split from the chimpanzees, are now called Hominina.
KNM-WT 17000 is a fossilized adult skull of the species Paranthropus aethiopicus. It was discovered in West Turkana, Kenya by Alan Walker in 1985. Estimated to be 2.5 million years old, the fossil is an adult with an estimated cranial capacity of 410 cc.
KNM ER 406 is an almost complete fossilized skull of the species Paranthropus boisei. It was discovered in Koobi Fora, Kenya by Richard Leakey and H. Mutua in 1969. This species is grouped with the Australopitecine genus, Paranthropus boisei because of the robusticity of the skull and the prominent characteristics. This species was found well preserved with a complete cranium but lacking dentition. He was known for his robust cranial features that showed the signs of adaptation of the ecological niches. The big chewing muscles attached to the sagittal crest are traits of this adaptation.
Post-canine megadontia is a relative enlargement of the molars and premolars compared to the size of the incisors and canines. This phenomenon is seen in some early hominid ancestors such as Paranthropus aethiopicus.
Australopithecus sediba is an extinct species of australopithecine recovered from Malapa Cave, Cradle of Humankind, South Africa. It is known from a partial juvenile skeleton, the holotype MH1, and a partial adult female skeleton, the paratype MH2. They date to about 1.98 million years ago in the Early Pleistocene, and coexisted with Paranthropus robustus and Homo ergaster / Homo erectus. Malapa Cave may have been a natural death trap, the base of a long vertical shaft which creatures could accidentally fall into. A. sediba was initially described as being a potential human ancestor, and perhaps the progenitor of Homo, but this is contested and it could also represent a late-surviving population or sister species of A. africanus which had earlier inhabited the area.
Changes to the dental morphology and jaw are major elements of hominid evolution. These changes were driven by the types and processing of food eaten. The evolution of the jaw is thought to have facilitated encephalization, speech, and the formation of the uniquely human chin.
Australopithecus deyiremeda is an extinct species of australopithecine from Woranso–Mille, Afar Region, Ethiopia, about 3.5 to 3.3 million years ago during the Pliocene. Because it is known only from three partial jawbones, it is unclear if these specimens indeed represent a unique species or belong to the much better-known A. afarensis. A. deyiremeda is distinguished by its forward-facing cheek bones and small cheek teeth compared to those of other early hominins. It is unclear if a partial foot specimen exhibiting a dextrous big toe can be assigned to A. deyiremeda. A. deyiremeda lived in a mosaic environment featuring both open grasslands and lake- or riverside forests, and anthropologist Fred Spoor suggests it may have been involved in the Kenyan Lomekwi stone-tool industry typically assigned to Kenyanthropus. A. deyiremeda coexisted with A. afarensis, and they may have exhibited niche partitioning to avoid competing with each other for the same resources, such as by relying on different fallback foods during leaner times.