Human taxonomy


Human taxonomy is the classification of the human species within zoological taxonomy. The systematic genus, Homo, is designed to include both anatomically modern humans and extinct varieties of archaic humans. Current humans have been designated as subspecies Homo sapiens sapiens, differentiated according to some from the direct ancestor, Homo sapiens idaltu.
Since the introduction of systematic names in the 18th century, knowledge of human evolution has increased drastically, and a number of intermediate taxa have been proposed in the 20th to early 21st century. The most widely accepted taxonomy groups takes the genus Homo as originating between two and three million years ago, divided into at least two species, archaic Homo erectus and modern Homo sapiens, with about a dozen further suggestions for species without universal recognition.
The genus Homo is placed in the tribe Hominini alongside Pan. The two genera are estimated to have diverged over an extended time of hybridization spanning roughly 10 to 6 million years ago, with possible admixture as late as 4 million years ago. A subtribe of uncertain validity, grouping archaic "pre-human" or "para-human" species younger than the Homo-Pan split is Australopithecina.
A proposal by Wood and Richmond would introduce Hominina as a subtribe alongside Australopithecina, with Homo the only known genus within Hominina. Alternatively, following Cela-Conde and Ayala, the "pre-human" or "proto-human" genera of Australopithecus, Ardipithecus, Praeanthropus, and possibly Sahelanthropus may be placed on equal footing alongside the genus Homo. An even more radical view rejects the division of Pan and Homo as separate genera, which based on the Principle of Priority would imply the reclassification of chimpanzees as Homo paniscus.
Prior to the current scientific classification of humans, philosophers and scientists have made various attempts to classify humans. They offered definitions of the human being and schemes for classifying types of humans. Biologists once classified races as subspecies, but today anthropologists reject the concept of race and view humanity as an interrelated genetic continuum. Taxonomy of the hominins continues to evolve.

History

Human taxonomy on one hand involves the placement of humans within the Taxonomy of the hominids, and on the other the division of archaic and modern humans into species and, if applicable, subspecies. Modern zoological taxonomy was developed by Carl Linnaeus during the 1730s to 1750s. He named the human species as Homo sapiens in 1758, as the only member species of the genus Homo, divided into [|several subspecies] corresponding to the great races. The Latin noun means "human being". The systematic name Hominidae for the family of the great apes was introduced by John Edward Gray. Gray also supplied Hominini as the name of the tribe including both chimpanzees and humans.
The discovery of the first extinct archaic human species from the fossil record dates to the mid 19th century, Homo neanderthalensis, classified in 1864. Since then, a number of other archaic species have been named, but there is no universal consensus as to their exact number. After the discovery of H. neanderthalensis, which even if "archaic" is recognizable as clearly human, late 19th to early 20th century anthropology for a time was occupied with finding the supposedly "missing link" between Homo and Pan. The "Piltdown Man" hoax of 1912 was the fraudulent presentation of such a transitional species. Since the mid-20th century, knowledge of the development of Hominini has become much more detailed, and taxonomical terminology has been altered a number of times to reflect this.
The introduction of Australopithecus as a third genus, alongside Homo and Pan, in the tribe Hominini is due to Raymond Dart. Australopithecina as a subtribe containing Australopithecus as well as Paranthropus is a proposal by Gregory & Hellman. More recently proposed additions to the Australopithecina subtribe include Ardipithecus and Kenyanthropus. The position of Sahelanthropus relative to Australopithecina within Hominini is unclear. Cela-Conde and Ayala propose the recognition of Australopithecus, Ardipithecus, Praeanthropus, and Sahelanthropus as separate genera.
Other proposed genera, now mostly considered part of Homo, include:
Pithecanthropus,
Protanthropus,
Sinanthropus,
Cyphanthropus
Africanthropus,
Telanthropus,
Atlanthropus,
Tchadanthropus.
The genus Homo has been taken to originate some two million years ago, since the discovery of stone tools in Olduvai Gorge, Tanzania, in the 1960s. Homo habilis would be the first "human" species by definition, its type specimen being the OH 7 fossils. However, the discovery of more fossils of this type has opened up the debate on the delineation of H. habilis from Australopithecus. Especially, the LD 350-1 jawbone fossil discovered in 2013, dated to 2.8 Mya, has been argued as being transitional between the two. It is also disputed whether H. habilis was the first hominin to use stone tools, as Australopithecus garhi, dated to c. 2.5 Mya, has been found along with stone tool implements. Fossil KNM-ER 1470 is now seen as either a third early species of Homo at about 2 million years ago, or alternatively as transitional between Australopithecus and Homo.
Wood and Richmond proposed that Gray's tribe Hominini be designated as comprising all species after the chimpanzee-human last common ancestor by definition, to the inclusion of Australopithecines and other possible pre-human or para-human species not known in Gray's time. In this suggestion, the new subtribe of Hominina was to be designated as including the genus Homo exclusively, so that Hominini would have two subtribes, Australopithecina and Hominina, with the only known genus in Hominina being Homo. Orrorin has been proposed as a possible ancestor of Hominina but not Australopithecina.
Designations alternative to Hominina have been proposed: Australopithecinae and Preanthropinae ;

Species

At least a dozen species of Homo other than Homo sapiens have been proposed, with varying degrees of consensus. Homo erectus is widely recognized as the species directly ancestral to Homo sapiens. Most other proposed species are proposed as alternatively belonging to either Homo erectus or Homo sapiens as a subspecies. This concerns Homo ergaster in particular. One proposal divides Homo erectus into an African and an Asian variety; the African is Homo ergaster, and the Asian is Homo erectus sensu stricto. There appears to be a recent trend, with the availability of ever more difficult-to-classify fossils such as the Dmanisi skulls or Homo naledi fossils to subsume all archaic varieties under Homo erectus.

Subspecies

''Homo sapiens'' subspecies

The recognition or nonrecognition of subspecies of Homo sapiens has a complicated history. The rank of subspecies in zoology is introduced for convenience, and not by objective criteria, based on pragmatic consideration of factors such as geographic isolation and sexual selection. The informal taxonomic rank of race is variously considered equivalent or subordinate to the rank of subspecies, and the division of anatomically modern humans into subspecies is closely tied to the recognition of major racial groupings based on human genetic variation.
A subspecies cannot be recognized independently: a species will either be recognized as having no subspecies at all or at least two. Therefore, the designation of an extant subspecies Homo sapiens sapiens only makes sense if at least one other subspecies is recognized. H. s. sapiens is attributed to "Linnaeus " by the taxonomic Principle of Coordination. William Stearn in a "passing remark" argued that Linnaeus "must stand as the type of his Homo sapiens". Since Linnaeus describes H. s. europaeus as having blue/green eyes but himself had brown eyes, he cannot have included himself in H. s. europaeus, Linnaeus would therefore have to be classified as H. sapiens sapiens, as not matching any of the descriptions of his five subspecies, and so would stand as the lectotype both for H. sapiens, and for H. s. sapiens within his own subspecies nomenclature.
During the 19th to mid-20th century, it was common practice to classify the major divisions of extant H. sapiens as subspecies, following Linnaeus, who had recognized H. s. americanus, H. s. europaeus, H. s. asiaticus and H. s. afer as grouping the native populations of the Americas, West Eurasia, East Asia and Sub-Saharan Africa, respectively, besides H. s. ferus and two further "wild" forms for reported specimens now considered part of cryptozoology, H. s. monstrosus and H. s. troglodytes.
There were variations and additions to the categories of Linnaeus, such as H. s. tasmanianus for the native population of Australia. Bory de St. Vincent in his Essai sur l'Homme extended Linné's "racial" categories to as many as fifteen: Leiotrichi : japeticus, arabicus, indicus, scythicus, sinicus, hyperboreus, neptunianus, australasicus, columbicus, americanus, patagonicus; Oulotrichi : aethiopicus, cafer, hottentotus, melaninus. Similarly, Georges Vacher de Lapouge also had categories based on race, such as priscus, spelaeus.
Homo sapiens neanderthalensis was proposed by King as an alternative to Homo neanderthalensis. There have been "taxonomic wars" over whether Neanderthals were a separate species since their discovery in the 1860s. Pääbo frames this as a debate that is unresolvable in principle, "since there is no definition of species perfectly describing the case." Louis Lartet proposed Homo sapiens fossilis based on the Cro-Magnon fossils.
There are a number of proposals of extinct varieties of Homo sapiens made in the 20th century. Many of the original proposals were not using explicit trinomial nomenclature, even though they are still cited as valid synonyms of H. sapiens by Wilson & Reeder. These include: Homo grimaldii,
Homo aurignacensis hauseri,
Notanthropus eurafricanus,
Homo fossilis infrasp. proto-aethiopicus,
Telanthropus capensis,
Homo wadjakensis,
Homo sapiens cro-magnonensis, Homo sapiens grimaldiensis,
Homo drennani,
Homo galilensis = Paleanthropus palestinus.
Rightmire proposed Homo sapiens rhodesiensis.
By the 1980s, the practice of dividing extant populations of Homo sapiens into subspecies declined. An early authority explicitly avoiding the division of H. sapiens into subspecies was Grzimeks Tierleben, published 1967-1972.
A late example of an academic authority proposing that the human racial groups should be considered taxonomical subspecies is John Baker. The trinomial nomenclature Homo sapiens sapiens became popular for "modern humans" in the context of Neanderthals being considered a subspecies of H. sapiens in the second half of the 20th century. Derived from the convention, widespread in the 1980s, of considering two subspecies, H. s. neanderthalensis and H. s. sapiens, the explicit claim that "H. s. sapiens is the only extant human subspecies" appears in the early 1990s.
Since the 2000s, the extinct Homo sapiens idaltu has gained wide recognition as a subspecies of Homo sapiens, but even in this case there is a dissenting view arguing that "the skulls may not be distinctive enough to warrant a new subspecies name". H. s. neanderthalensis and H. s. rhodesiensis continue to be considered separate species by some authorities, but the 2010s discovery of genetic evidence of archaic human admixture with modern humans has reopened the details of taxonomy of archaic humans.

''Homo erectus'' subspecies

Homo erectus since its introduction in 1892 has been divided into numerous subspecies, many of them formerly considered individual species of Homo. None of these subspecies have universal consensus among paleontologists.