Human evolution

This article is about the general evolution of humans. For a timeline of a human evolution, click here.

Human evolution, or anthropogenesis, is the part of biological evolution concerning the emergence of Homo sapiens as a distinct species from other hominins, great apes and placental mammals. It is the subject of a broad scientific inquiry that seeks to understand and describe how this change occurred. The study of human evolution encompasses many scientific disciplines, most notably physical anthropology, primatology, archaeology, linguistics and genetics.

The term "human", in the context of human evolution, refers to the genus Homo, but studies of human evolution usually include other hominins, such as the Australopithecines. The Homo genus diverged from the Australopithecines about 2 million years ago in Africa. Scientists have estimated that humans branched off from their common ancestor with chimpanzees—the only other living homininis—about 5–7 million years ago. Several "species" of Homo evolved or are now extinct. These include Homo erectus, which inhabited Asia, and Homo neanderthalensis, which inhabited Europe. Archaic Homo sapiens evolved between 400,000 and 250,000 years ago.

The dominant view among scientists is the recent African origin of modern humans that H. sapiens evolved in Africa and spread across the globe, replacing populations of H. erectus and H. neanderthalensis. Scientists supporting the alternative hypothesis, the multiregional origin of modern humans, view that modern humans evolved as separate populations stemming from a migration of H. erectus nearly 2.5 million years ago. The fossil evidence were insufficient to Leakey to resolve this vigorous debate,. Studies of haplogroups in Y-chromosomal DNA and mitochondrial DNA have largely supported a recent African origin, while evidence from nuclear genes supports a multiregional evolution. 2009 statistical analysis over available NIH data find evidence for ancient admixture, suggesting this may be a general feature of recent human evolution

History of ideas about human evolution

The word homo, the name of the biological genus to which humans belong, is Latin for "human". It was chosen originally by Carolus Linnaeus in his classification system. The word "human" is from the Latin humanus, the adjectival form of homo. The Latin "homo" derives from the Indo-European root, dhghem, or "earth".

Carolus Linnaeus and other scientists of his time also considered the great apes to be the closest relatives of human beings due to morphological and anatomical similarities. The possibility of linking humans with earlier apes by descent only became clear after 1859 with the publication of Charles Darwin's On the Origin of Species. This argued for the idea of the evolution of new species from earlier ones. Darwin's book did not address the question of human evolution, saying only that "Light will be thrown on the origin of man and his history".

The first debates about the nature of human evolution arose between Thomas Huxley and Richard Owen. Huxley argued for human evolution from apes by illustrating many of the similarities and differences between humans and apes and did so particularly in his 1863 book Evidence as to Man's Place in Nature. However, many of Darwin's early supporters (such as Alfred Russel Wallace and Charles Lyell) did not agree that the origin of the mental capacities and the moral sensibilities of humans could be explained by natural selection. Darwin applied the theory of evolution and sexual selection to humans when he published The Descent of Man in 1871.

A major problem was the lack of fossil intermediaries. It was only in the 1920s that such fossils were discovered in Africa. In 1925, Raymond Dart described Australopithecus africanus. The type specimen was the Taung Child, an Australopithecine infant discovered in a cave. The child's remains were a remarkably well-preserved tiny skull and an endocranial cast of the individual's brain. Although the brain was small (410 cm³), its shape was rounded, unlike that of chimpanzees and gorillas, and more like a modern human brain. Also, the specimen showed short canine teeth, and the position of the foramen magnum was evidence of bipedal locomotion. All of these traits convinced Dart that the Taung baby was a bipedal human ancestor, a transitional form between apes and humans.

The classification of humans and their relatives has changed considerably over time. The gracile Australopithecines are now thought to be ancestors of the genus Homo, the group to which modern humans belong. Both Australopithecines and Homo sapiens are part of the tribe Hominini. Recent data suggests Australopithecines were a diverse group and that A. africanus may not be a direct ancestor of modern humans. Reclassification of Australopithecines that originally were split into either gracile or robust varieties has put the latter into a family of its own, Paranthropus. Taxonomists place humans, Australopithecines and related species in the same family as other great apes, in the Hominidae.

Before Homo

Evolution of apes

The evolutionary history of the primates can be traced back 65 million years, as one of the oldest of all surviving placental mammal groups. The oldest known primates come from North America, but they were widespread in Eurasia and Africa during the tropical conditions of the Paleocene and Eocene.

With the beginning of modern climates, marked by the formation of the first Antarctic ice in the early Oligocene around 30 million years ago, primates went extinct everywhere but Africa and southern Asia. A primate from this time was Notharctus. Fossil evidence found in Germany in the 1980s was determined to be about 16.5 million years old, some 1.5 million years older than similar species from East Africa. It suggests that the primate lineage of the great apes first appeared in Eurasia and not Africa.

The early ancestors of the hominids (the family of great apes and humans) probably migrated to Eurasia from Africa about 17 million years ago, just before these two continents were cut off from each other by an expansion of the Mediterranean Sea. Begun says that these primates flourished in Eurasia and that the lineage leading to the African apes and humans— including Dryopithecus—migrated south from Europe or Western Asia into Africa. The surviving tropical population, which is seen most completely in the upper Eocene and lowermost Oligocene fossil beds of the Fayum depression southwest of Cairo, gave rise to all living primates—lemurs of Madagascar, lorises of Southeast Asia, galagos or "bush babies" of Africa, and the anthropoids; platyrrhines or New World monkeys, and catarrhines or Old World monkeys and the great apes and humans.

The earliest known catarrhine is Kamoyapithecus from uppermost Oligocene at Eragaleit in the northern Kenya Rift Valley, dated to 24 million years ago. Its ancestry is generally thought to be species related to Aegyptopithecus, Propliopithecus, and Parapithecus from the Fayum, at around 35 million years ago. There are no fossils from the intervening 11 million years.

In the early Miocene, after 22 million years ago, the many kinds of arboreally-adapted primitive catarrhines from East Africa suggest a long history of prior diversification. Fossils at 20 million years ago include fragments attributed to Victoriapithecus, the earliest Old World Monkey. Among the genera thought to be in the ape lineage leading up to 13 million years ago are Proconsul, Rangwapithecus, Dendropithecus, Limnopithecus, Nacholapithecus, Equatorius, Nyanzapithecus, Afropithecus, Heliopithecus, and Kenyapithecus, all from East Africa. The presence of other generalized non-cercopithecids of middle Miocene age from sites far distant—Otavipithecus from cave deposits in Namibia, and Pierolapithecus and Dryopithecus from France, Spain and Austria—is evidence of a wide diversity of forms across Africa and the Mediterranean basin during the relatively warm and equable climatic regimes of the early and middle Miocene. The youngest of the Miocene hominoids, Oreopithecus, is from 9 million year old coal beds in Italy.

Molecular evidence indicates that the lineage of gibbons (family Hylobatidae) became distinct from Great Apes between 18 and 12 million years ago, and that of orangutans (subfamily Ponginae) became distinct from the other Great Apes at about 12 million years; there are no fossils that clearly document the ancestry of gibbons, which may have originated in a so-far-unknown South East Asian hominoid population, but fossil proto-orangutans may be represented by Ramapithecus from India and Griphopithecus from Turkey, dated to around 10 million years ago.

Divergence of the human lineage from other Great Apes

Species close to the last common ancestor of gorillas, chimpanzees and humans may be represented by Nakalipithecus fossils found in Kenya and Ouranopithecus found in Greece. Molecular evidence suggests that between 8 and 4 million years ago, first the gorillas, and then the chimpanzees (genus Pan) split off from the line leading to the humans; human DNA is approximately 98.4% identical to that of chimpanzees when comparing single nucleotide polymorphisms (see Human evolutionary genetics). The fossil record of gorillas and chimpanzees is quite limited. Both poor preservation (rain forest soils tend to be acidic and dissolve bone) and sampling bias probably contribute to this problem.

Other hominines likely adapted to the drier environments outside the equatorial belt, along with antelopes, hyenas, dogs, pigs, elephants, and horses. The equatorial belt contracted after about 8 million years ago. Fossils of these hominans - the species in the human lineage following divergence from the chimpanzees - are relatively well known. The earliest are Sahelanthropus tchadensis (7 Ma) and Orrorin tugenensis (6 Ma), followed by:

• Ardipithecus (5.5–4.4 Ma), with species Ar. kadabba and Ar. ramidus;
• Australopithecus (4–2 Ma), with species Au. anamensis, Au. afarensis, Au. africanus, Au. bahrelghazali, and Au. garhi;
• Kenyanthropus (3–2.7 Ma), with species Kenyanthropus platyops
• Paranthropus (3–1.2 Ma), with species P. aethiopicus, P. boisei, and P. robustus;
• Homo (2 Ma–present), with species Homo habilis, Homo rudolfensis, Homo ergaster, Homo georgicus, Homo antecessor, Homo cepranensis, Homo erectus, Homo heidelbergensis, Homo rhodesiensis, Homo neanderthalensis, Homo sapiens idaltu, Archaic Homo sapiens, Homo floresiensis

Genus Homo

Homo sapiens is the only non-extinct species of its genus, Homo. There were other Homo species, all of which are now extinct. While some of these other species might have been ancestors of H. sapiens, many were likely our "cousins", having speciated away from our ancestral line. There is not yet a consensus as to which of these groups should count as separate species and which as subspecies. In some cases this is due to the paucity of fossils, in other cases it is due to the slight differences used to classify species in the Homo genus. The Sahara pump theory provides an explanation of the early variation in the genus Homo.

Based on archaeological and paleontological evidence, it has been possible to infer the ancient dietary practices of various Homo species and to study the role of diet in physical and behavioral evolution within Homo.

Homo habilis

H. habilis lived from about 2.4 to 1.4 Ma. H. habilis, the first species of the genus Homo, evolved in South and East Africa in the late Pliocene or early Pleistocene, 2.5–2 Ma, when it diverged from the Australopithecines. H. habilis had smaller molars and larger brains than the Australopithecines, and made tools from stone and perhaps animal bones. One of the first known hominids, it was nicknamed 'handy man' by its discoverer, Louis Leakey due to its association with stone tools. Some scientists have proposed moving this species out of Homo and into Australopithecus due to the morphology of its skeleton being more adapted to living on trees rather than to moving on two legs like H. sapiens.

Homo rudolfensis and Homo georgicus

These are proposed species names for fossils from about 1.9–1.6 Ma, the relation of which with H. habilis is not yet clear.

• H. rudolfensis refers to a single, incomplete skull from Kenya. Scientists have suggested that this was another H. habilis, but this has not been confirmed.
• H. georgicus, from Georgia, may be an intermediate form between H. habilis and H. erectus, or a sub-species of H. erectus.

Homo ergaster and Homo erectus

One current view of the temporal and geographical distribution of hominid populations. Other interpretations differ mainly in the taxonomy and geographical distribution of hominid species.

The first fossils of Homo erectus were discovered by Dutch physician Eugene Dubois in 1891 on the Indonesian island of Java. He originally gave the material the name Pithecanthropus erectus based on its morphology that he considered to be intermediate between that of humans and apes. H. erectus lived from about 1.8 Ma to about 70,000 years ago (which would indicate that they were probably wiped out by the Toba catastrophe). Often the early phase, from 1.8 to 1.25 Ma, is considered to be a separate species, H. ergaster, or it is seen as a subspecies of H. erectus, Homo erectus ergaster.

In the early Pleistocene, 1.5–1 Ma, in Africa, Asia, and Europe, some populations of Homo habilis are thought to have evolved larger brains and made more elaborate stone tools; these differences and others are sufficient for anthropologists to classify them as a new species, H. erectus. In addition H. erectus was the first human ancestor to walk truly upright. This was made possible by the evolution of locking knees and a different location of the foramen magnum (the hole in the skull where the spine enters). They may have used fire to cook their meat.

See also: Control of fire by early humans

A famous example of Homo erectus is Peking Man; others were found in Asia (notably in Indonesia), Africa, and Europe. Many paleoanthropologists now use the term Homo ergaster for the non-Asian forms of this group, and reserving H. erectus only for those fossils found in the Asian region and meeting certain skeletal and dental requirements which differ slightly from H. ergaster.

Homo cepranensis and Homo antecessor

These are proposed as species that may be intermediate between H. erectus and H. heidelbergensis.

• H. antecessor is known from fossils from Spain and England that are dated 1.2 Ma–500 ka.
• H. cepranensis refers to a single skull cap from Italy, estimated to be about 800,000 years old.

Homo heidelbergensis

H. heidelbergensis (Heidelberg Man) lived from about 800,000 to about 300,000 years ago. Also proposed as Homo sapiens heidelbergensis or Homo sapiens paleohungaricus.

Homo rhodesiensis, and the Gawis cranium

• H. rhodesiensis, estimated to be 300,000–125,000 years old. Most current experts believe Rhodesian Man to be within the group of Homo heidelbergensis though other designations such as Archaic Homo sapiens and Homo sapiens rhodesiensis have also been proposed.
• In February 2006 a fossil, the Gawis cranium, was found which might possibly be a species intermediate between H. erectus and H. sapiens or one of many evolutionary dead ends. The skull from Gawis, Ethiopia, is believed to be 500,000–250,000 years old. Only summary details are known, and no peer reviewed studies have been released by the finding team. Gawis man's facial features suggest its being either an intermediate species or an example of a "Bodo man" female.

Homo neanderthalensis

H. neanderthalensis lived from 400,000 or about 250,000 to as recent as 30,000 years ago. Also proposed as Homo sapiens neanderthalensis: there is ongoing debate over whether the 'Neanderthal Man' was a separate species, Homo neanderthalensis, or a subspecies of H. sapiens While the debate remains unsettled, evidence from sequencing mitochondrial DNA indicates that no significant gene flow occurred between H. neanderthalensis and H. sapiens, and, therefore, the two were separate species that shared a common ancestor about 660,000 years ago. In 1997, Mark Stoneking stated: "These results [based on mitochondrial DNA extracted from Neanderthal bone] indicate that Neanderthals did not contribute mitochondrial DNA to modern humans… Neanderthals are not our ancestors." Subsequent investigation of a second source of Neanderthal DNA supported these findings. However, supporters of the multiregional hypothesis point to recent studies indicating non-African nuclear DNA heritage dating to one Ma, although the reliability of these studies has been questioned. Competition from Homo sapiens probably contributed to Neanderthal extinction.

Homo sapiens

Main article: Early Homo sapiens

H. sapiens ("sapiens" is Latin for wise or intelligent) has lived from about 250,000 years ago to the present. Between 400,000 years ago and the second interglacial period in the Middle Pleistocene, around 250,000 years ago, the trend in skull expansion and the elaboration of stone tool technologies developed, providing evidence for a transition from H. erectus to H. sapiens. The direct evidence suggests there was a migration of H. erectus out of Africa, then a further speciation of H. sapiens from H. erectus in Africa. A subsequent migration within and out of Africa eventually replaced the earlier dispersed H. erectus. This migration and origin theory is usually referred to as the recent single origin or Out of Africa theory. Current evidence does not preclude some multiregional evolution or some admixture of the migrant H. sapiens with existing Homo populations. This is a hotly debated area of paleoanthropology.

Current research has established that human beings are genetically highly homogenous; that is, the DNA of individuals is more alike than usual for most species, which may have resulted from their relatively recent evolution or the Toba catastrophe. Distinctive genetic characteristics have arisen, however, primarily as the result of small groups of people moving into new environmental circumstances. These adapted traits are a very small component of the Homo sapiens genome, but include various characteristics such as skin color and nose form, in addition to internal characteristics such as the ability to breathe more efficiently in high altitudes.

H. sapiens idaltu, from Ethiopia, is a possible extinct sub-species who lived from about 160,000 years ago. It is the oldest known anatomically modern human.

Homo floresiensis

Main article: Homo floresiensis

H. floresiensis, which lived from approximately 100,000 to 12,000 before present, has been nicknamed hobbit for its small size, possibly a result of insular dwarfism. H. floresiensis is intriguing both for its size and its age, being a concrete example of a recent species of the genus Homo that exhibits derived traits not shared with modern humans. In other words, H. floresiensis share a common ancestor with modern humans, but split from the modern human lineage and followed a distinct evolutionary path. The main find was a skeleton believed to be a woman of about 30 years of age. Found in 2003 it has been dated to approximately 18,000 years old. The living woman was estimated to be one meter in height, with a brain volume of just 380 cm³ (considered small for a chimpanzee and less than a third of the H. sapiens average of 1400 cm³).

However, there is an ongoing debate over whether H. floresiensis is indeed a separate species. Some scientists presently believe that H. floresiensis was a modern H. sapiens suffering from pathological dwarfism. This hypothesis is supported in part, because some modern humans who live on Flores, the island where the skeleton was found, are pygmies. This coupled with pathological dwarfism could indeed create a hobbit-like human. The other major attack on H. floresiensis is that it was found with tools only associated with H. sapiens.

Comparative table of Homo species

Comparative table of Homo lineages

Lineages	Temporal range (kya)	Habitat	Adult height	Adult mass	Cranial capacity (cm3)	Fossil record	Discovery	Publication of name
H. habilis membership in Homo uncertain	2,100–1,500	Tanzania	110–140 cm (3 ft 7 in – 4 ft 7 in)	33–55 kg (73–121 lb)	510–660	Many	1960	1964
H. rudolfensis membership in Homo uncertain	1,900	Kenya			700	2 sites	1972	1986
H. gautengensis also classified as H. habilis	1,900–600	South Africa	100 cm (3 ft 3 in)			3 individuals	2010	2010
H. erectus	1,900–140	Africa, Eurasia	180 cm (5 ft 11 in)	60 kg (130 lb)	850 (early) – 1,100 (late)	Many	1891	1892
H. ergaster African H. erectus	1,800–1,300	East and Southern Africa			700–850	Many	1949	1975
H. antecessor	1,200–800	Western Europe	175 cm (5 ft 9 in)	90 kg (200 lb)	1,000	2 sites	1994	1997
H. heidelbergensis early H. neanderthalensis	600–300	Europe, Africa	180 cm (5 ft 11 in)	90 kg (200 lb)	1,100–1,400	Many	1907	1908
H. cepranensis a single fossil, possibly H. heidelbergensis	c. 450	Italy			1,000	1 skull cap	1994	2003
H. longi	309–138	Northeast China			1,420	1 individual	1933	2021
H. rhodesiensis early H. sapiens	c. 300	Zambia			1,300	Single or very few	1921	1921
H. naledi	c. 300	South Africa	150 cm (4 ft 11 in)	45 kg (99 lb)	450	15 individuals	2013	2015
H. sapiens (anatomically modern humans)	c. 300–present	Worldwide	150–190 cm (4 ft 11 in – 6 ft 3 in)	50–100 kg (110–220 lb)	950–1,800	(extant)	——	1758
H. neanderthalensis	240–40	Europe, Western Asia	170 cm (5 ft 7 in)	55–70 kg (121–154 lb) (heavily built)	1,200–1,900	Many	1829	1864
H. floresiensis classification uncertain	190–50	Indonesia	100 cm (3 ft 3 in)	25 kg (55 lb)	400	7 individuals	2003	2004
Nesher Ramla Homo classification uncertain	140–120	Israel				several individuals	2021
H. tsaichangensis possibly H. erectus or Denisova	c. 100	Taiwan				1 individual	2008(?)	2015
H. luzonensis	c. 67	Philippines				3 individuals	2007	2019
Denisova hominin	40	Siberia				2 sites	2000	2010

Use of tools

See also: Hunting hypothesis

Using tools has been interpreted as a sign of intelligence, and it has been theorized that tool use may have stimulated certain aspects of human evolution—most notably the continued expansion of the human brain. Paleontology has yet to explain the expansion of this organ over millions of years despite being extremely demanding in terms of energy consumption. The brain of a modern human consumes about 20 watts (400 kilocalories per day), which is one fifth of the energy consumption of a human body. Increased tool use would allow hunting for energy-rich meat products, and would enable processing more energy-rich plant products. Researchers have suggested that early hominids were thus under evolutionary pressure to increase their capacity to create and use tools.

Precisely when early humans started to use tools is difficult to determine, because the more primitive these tools are (for example, sharp-edged stones) the more difficult it is to decide whether they are natural objects or human artifacts. There is some evidence that the australopithecines (4 Ma) may have used broken bones as tools, but this is debated.

It should be noted that many species make and use tools, but it is the human species that dominates the areas of making and using more complex tools. A good question is, what species made and used the first tools? The oldest known tools are the "Oldowan stone tools" from Ethiopia. It was discovered that these tools are from 2.5 to 2.6 million years old, which predates the earliest known "Homo" species. There is no known evidence that any "Homo" specimens appeared by 2.5 Ma. A Homo fossil was found near some Oldowan tools, and its age was noted at 2.3 million years old, suggesting that maybe the Homo species did indeed create and use these tools. It is surely possible, but not solid evidence. Bernard Wood noted that "Paranthropus" coexisted with the early Homo species in the area of the "Oldowan Industrial Complex" over roughly the same span of time. Although there is no direct evidence that points to Paranthropus as the tool makers, their anatomy lends to indirect evidence of their capabilities in this area. Most paleoanthropologists agree that the early "Homo" species were indeed responsible for most of the Oldowan tools found. They argue that when most of the Oldowan tools were found in association with human fossils, Homo was always present, but Paranthropus was not.

In 1994, Randall Susman used the anatomy of opposable thumbs as the basis for his argument that both the Homo and Paranthropus species were toolmakers. He compared bones and muscles of human and chimpanzee thumbs, finding that humans have 3 muscles that chimps lack. Humans also have thicker metacarpals with broader heads, making the human hand more successful at precision grasping than the chimpanzee hand. Susman defended that modern anatomy of the human thumb is an evolutionary response to the requirements associated with making and handling tools and that both species were indeed toolmakers.

Stone tools

Stone tools are first attested around 2.6 Ma, when H. habilis in Eastern Africa used so-called pebble tools, choppers made out of round pebbles that had been split by simple strikes. This marks the beginning of the Paleolithic, or Old Stone Age; its end is taken to be the end of the last Ice Age, around 10,000 years ago. The Paleolithic is subdivided into the Lower Paleolithic (Early Stone Age, ending around 350,000–300,000 years ago), the Middle Paleolithic (Middle Stone Age, until 50,000–30,000 years ago), and the Upper Paleolithic.

The period from 700,000–300,000 years ago is also known as the Acheulean, when H. ergaster (or erectus) made large stone hand-axes out of flint and quartzite, at first quite rough (Early Acheulian), later "retouched" by additional, more subtle strikes at the sides of the flakes. After 350,000 BP (Before Present) the more refined so-called Levallois technique was developed. It consisted of a series of consecutive strikes, by which scrapers, slicers ("racloirs"), needles, and flattened needles were made. Finally, after about 50,000 BP, ever more refined and specialized flint tools were made by the Neanderthals and the immigrant Cro-Magnons (knives, blades, skimmers). In this period they also started to make tools out of bone.

Modern humans and the "Great Leap Forward" debate

See also: Behavioral modernity

Until about 50,000–40,000 years ago the use of stone tools seems to have progressed stepwise. Each phase (H. habilis, H. ergaster, H. neanderthalensis) started at a higher level than the previous one, but once that phase started further development was slow. These Homo species were culturally conservative, but after 50,000 BP modern human culture started to change at a much greater speed. Jared Diamond, author of The Third Chimpanzee, and other anthropologists characterize this as a "Great Leap Forward."

Modern humans started burying their dead, making clothing out of hides, developing sophisticated hunting techniques (such as using trapping pits or driving animals off cliffs), and engaging in cave painting. As human culture advanced, different populations of humans introduced novelty to existing technologies: artifacts such as fish hooks, buttons and bone needles show signs of variation among different populations of humans, something that had not been seen in human cultures prior to 50,000 BP. Typically, H. neanderthalensis populations do not vary in their technologies.

Modern human behavior includes four aspects: abstract thinking (concepts free from specific examples), planning (taking steps to achieve a further goal), innovation (finding new solutions), and symbolic behaviour (such as images and rituals). Among concrete examples of modern human behavior, anthropologists include specialization of tools, use of jewelery and images (such as cave drawings), organization of living space, rituals (for example, burials with grave gifts), specialized hunting techniques, exploration of less hospitable geographical areas, and barter trade networks. Debate continues as to whether a "revolution" led to modern humans ("the big bang of human consciousness"), or whether the evolution was more gradual.

Models of human evolution

Today, all humans belong to one, undivided by species barrier, population of Homo sapiens sapiens.. However, according to "Out of Africa" this is not the first species of hominids: the first species of genus Homo, Homo habilis, evolved in East Africa at least 2 Ma, and members of this species populated different parts of Africa in a relatively short time. Homo erectus evolved more than 1.8 Ma, and by 1.5 Ma had spread throughout the Old World.

Anthropologists have been divided as to whether current human population evolved as one interconnected population (as postulated by the Multiregional Evolution hypothesis), or evolved only in East Africa, speciated, and then migrating out of Africa and replaced human populations in Eurasia (called the "Out of Africa" Model or the "Complete Replacement" Model).

Multiregional model

Main article: Multiregional hypothesis

Multiregional evolution a model to account for the pattern of human evolution, was proposed by Milford H. Wolpoff in 1988. Multiregional evolution holds that human evolution from the beginning of the Pleistocene 2.5 million years BP to the present day has been within a single, continuous human species, evolving worldwide to modern Homo sapiens.

According to multiregional evolution, fossil and genomic data are evidence for worldwide human evolution and contradict recent speciation postulated by RAO (the other hypothesis regarding human evolution).

2009 statistical analysis over available NIH data find evidence for ancient admixture, suggesting this may be a general feature of recent human evolution).

Out of Africa

See also: Recent single origin hypothesis and Early human migrations

According to the Out of Africa model, developed by Chris Stringer and Peter Andrews, modern H. sapiens evolved in Africa 200,000 years ago. Homo sapiens began migrating from Africa between 70,000 – 50,000 years ago and eventually replaced existing hominid species in Europe and Asia. Out of Africa has gained support from research using mitochondrial DNA (mtDNA). After analysing genealogy trees constructed using 133 types of mtDNA, researchers concluded that all were descended from a woman from Africa, dubbed Mitochondrial Eve. Out of Africa is also supported by the fact that mitochondrial genetic diversity is highest among African populations.

There are differing theories on whether there was a single exodus or several. A multiple dispersal model involves the Southern Dispersal theory, which has gained support in recent years from genetic, linguistic and archaeological evidence. In this theory, there was a coastal dispersal of modern humans from the Horn of Africa around 70,000 years ago. This group helped to populate Southeast Asia and Oceania, explaining the discovery of early human sites in these areas much earlier than those in the Levant. A second wave of humans dispersed across the Sinai peninsula into Asia, resulting in the bulk of human population for Eurasia. This second group possessed a more sophisticated tool technology and was less dependent on coastal food sources than the original group. Much of the evidence for the first group's expansion would have been destroyed by the rising sea levels at the end of the Holocene era. The multiple dispersal model is contradicted by studies indicating that the populations of Eurasia and the populations of Southeast Asia and Oceania are all descended from the same mitochondrial DNA lineages, which support a single migration out of Africa that gave rise to all non-African populations.

Genetics

Main article: Human evolutionary genetics

Human evolutionary genetics studies how one human genome differs from the other, the evolutionary past that gave rise to it, and its current effects. Differences between genomes have anthropological, medical and forensic implications and applications. Genetic data can provide important insight into human evolution.

Notable human evolution researchers

See also: Category:Human evolution theorists

• Robert Broom, a Scottish physician and palaeontologist whose work on South Africa led to the discovery and description of "Mrs. Ples"
• James Burnett, Lord Monboddo, a British judge most famous today as a founder of modern comparative historical linguistics
• Raymond Dart, an Australian anatomist and palaeoanthropologist, whose work at Taung, in South Africa, led to the discovery of Australopithecus africanus
• Charles Darwin, a British naturalist who documented considerable evidence that species originate through evolutionary change
• Richard Dawkins, a British ethologist, evolutionary biologist who has promoted a gene-centered view of evolution
• J. B. S. Haldane, a British geneticist and evolutionary biologist
• William D. Hamilton, a British Evolutionary Biologist who expounded a rigorous genetic basis for kin selection, and on the evolution of HIV and other human diseases.
• Sir Alister Hardy, a British zoologist, who first hypothesised the aquatic ape theory of human evolution
• Henry McHenry, an American anthropologist who specializes in studies of human evolution, the origins of bipedality, and paleoanthropology
• Louis Leakey, an African archaeologist and naturalist whose work was important in establishing human evolutionary development in Africa
• Mary Leakey, a British archaeologist and anthropologist whose discoveries in Africa include the Laetoli footprints
• Richard Leakey, an African paleontologist and archaeologist, son of Louis and Mary Leakey
• Svante Pääbo, a Swedish biologist specializing in evolutionary genetics
• Jeffrey H. Schwartz, an American physical anthropologist and professor of biological anthropology
• Chris Stringer, anthropologist, leading proponent of the recent single origin hypothesis
• Alan Templeton, geneticist and statistician, proponent of the multiregional hypothesis
• Philip V. Tobias, a South African palaeoanthropologist is one of the world's leading authorities on the evolution of humankind
• Erik Trinkaus, a prominent American paleoanthropologist and expert on Neanderthal biology and human evolution
• Milford H. Wolpoff, an American paleoanthropologist who is the leading proponent of the multiregional evolution hypothesis.

Species list

This list is in chronological order across the page by genus. Template:Multicol

• Sahelanthropus
  • Sahelanthropus tchadensis
• Orrorin
  • Orrorin tugenensis
• Ardipithecus
  • Ardipithecus kadabba
  • Ardipithecus ramidus

• Australopithecus
  • Australopithecus anamensis
  • Australopithecus afarensis
  • Australopithecus bahrelghazali
  • Australopithecus africanus
  • Australopithecus garhi
• Paranthropus
  • Paranthropus aethiopicus
  • Paranthropus boisei
  • Paranthropus robustus
• Kenyanthropus
  • Kenyanthropus platyops

• Homo
  • Homo habilis
  • Homo rudolfensis
  • Homo ergaster
  • Homo georgicus
  • Homo erectus
  • Homo cepranensis
  • Homo antecessor
  • Homo heidelbergensis
  • Homo rhodesiensis
  • Homo neanderthalensis
  • Homo sapiens idaltu
  • Homo sapiens (Cro-Magnon)
  • Homo sapiens sapiens
  • Homo floresiensis

See also

• List of human evolution fossils
• Timeline of human evolution
• Archaeogenetics
• Dual inheritance theory
• Dysgenics
• Evolutionary anthropology
• Evolutionary medicine
• Evolutionary neuroscience
• Evolution of human intelligence
• Evolution of morality
• Evolutionary origin of religions

• Evolutionary psychology
• History of Earth
• Hominid intelligence
• Human behavioral ecology
• Human skeletal changes due to bipedalism
• Human vestigiality
• Ida (fossil)
• Physical anthropology
• Sexual selection in human evolution
• Sociocultural evolution

Further reading

Main article: Bibliography of evolution and human behavior

• Alexander, R. D. (1990). "How Did Humans Evolve? Reflections on the Uniquely Unique Species" (PDF). University of Michigan Museum of Zoology Special Publication (1). University of Michigan Museum of Zoology: 1–38.
• Flinn, M. V., Geary, D. C., & Ward, C. V. (2005). Ecological dominance, social competition, and coalitionary arms races: Why humans evolved extraordinary intelligence. Evolution and Human Behavior, 26, 10-46. Template:PDFlink
• Jones, S., Martin, R., & Pilbeam, D. (Eds.). (1994). The Cambridge Encyclopedia of Human Evolution. Cambridge: Cambridge University Press.
• Wolfgang Enard; et al. (2002-08-22). "Molecular evolution of FOXP2, a gene involved in speech and language". Nature. 418: 870. {{cite journal}}: Explicit use of et al. in: |author= (help)
• DNA Shows Neandertals Were Not Our Ancestors
• J. W. IJdo, A. Baldini, D. C. Ward, S. T. Reeders, R. A. Wells (1991). "Origin of human chromosome 2: An ancestral telomere-telomere fusion" (PDF). Genetics. 88: 9051–9055. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)—two ancestral ape chromosomes fused to give rise to human chromosome 2.
• Ovchinnikov; et al. (2000). "Molecular analysis of Neanderthal DNA from the Northern Caucasus". Nature. 404: 490. doi:10.1038/35006625. {{cite journal}}: Explicit use of et al. in: |author= (help)
• Heizmann, Elmar P J, Begun, David R (2001). "The oldest Eurasian hominoid". Journal of Human Evolution. 41 (5): 463. doi:10.1006/jhev.2001.0495.{{cite journal}}: CS1 maint: multiple names: authors list (link)
• BBC: Finds test human origins theory. 2007-08-08 Homo habilis and Homo erectus are sister species that overlapped in time.

External links

• BBC: The Evolution of Man
• Illustrations from Evolution (textbook)
• Smithsonian – Homosapiens
• Smithsonian – The Human Origins Program
• Becoming Human: Paleoanthropology, Evolution and Human Origins, presented by Arizona State University's Institute of Human Origins