{"id":207313,"date":"2017-07-23T01:13:13","date_gmt":"2017-07-23T05:13:13","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/human-evolution-wikipedia\/"},"modified":"2017-07-23T01:13:13","modified_gmt":"2017-07-23T05:13:13","slug":"human-evolution-wikipedia","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/evolution\/human-evolution-wikipedia\/","title":{"rendered":"Human evolution &#8211; Wikipedia"},"content":{"rendered":"<p><p>      Human evolution, also known as hominization,      is the evolutionary process that led to the      emergence of anatomically modern humans,      beginning with the evolutionary      history of primates  in particular genus Homo  and leading to the emergence of      Homo      sapiens as a distinct species of the hominid      family, the great apes. This process involves the      gradually loss of typical animal characteristics and the      development of exclusively human properties.[1]    <\/p>\n<p>      The study of human evolution involves many scientific      disciplines, including physical anthropology, primatology,      archaeology, paleontology, neurobiology, ethology, linguistics, evolutionary psychology,      embryology      and genetics.[2] Genetic      studies show that primates diverged from other mammals about 85 million years ago, in the      Late      Cretaceous period, and the earliest fossils appear in the      Paleocene,      around 55 million years ago.[3]    <\/p>\n<p>      Within the Hominoidea (apes) superfamily, the      Hominidae      family diverged from the Hylobatidae (gibbon) family      some 1520 million years ago; African great apes (subfamily      Homininae)      diverged from orangutans (Ponginae) about 14 million years ago; the      Hominini tribe      (humans, Australopithecines and other extinct biped      genera, and chimpanzee) parted from the Gorillini tribe      (gorillas) between 9 million years ago and      8 million years ago; and, in      turn, the subtribes Hominina (humans and biped      ancestors) and Panina (chimps) separated about      7.5 million years ago to      5.6 million years ago.[4]    <\/p>\n<p>      Human evolution from its first separation from the last common ancestor      of humans and chimpanzees is characterized by a number of      morphological, developmental, physiological, and behavioral      changes. The most significant of these adaptations are      bipedalism, increased brain size, lengthened ontogeny (gestation and      infancy), and decreased sexual dimorphism. The      relationship between these changes is the subject of ongoing      debate.[5][pageneeded]      Other significant morphological changes included the      evolution of a power and precision grip, a change first      occurring in H. erectus.[6]    <\/p>\n<p>      Bipedalism is the basic adaptation of the      hominid and is considered the main cause behind a suite of      skeletal      changes shared by all bipedal hominids. The earliest      hominin, of presumably primitive bipedalism, is considered to      be either Sahelanthropus[7] or Orrorin, both of      which arose some 6 to 7 million years ago. The non-bipedal      knuckle-walkers, the gorilla and chimpanzee, diverged from      the hominin line over a period covering the same time, so      either of Sahelanthropus or Orrorin may be our      last shared      ancestor. Ardipithecus, a full biped, arose      somewhat later.[citation      needed]    <\/p>\n<p>      The early bipeds eventually evolved into the      australopithecines and still later into the genus      Homo. There are several theories of the adaptation      value of bipedalism. It is possible that bipedalism was      favored because it freed the hands for reaching and carrying      food, saved energy during locomotion,[8]      enabled long distance running and hunting, provided an      enhanced field of vision, and helped avoid hyperthermia by      reducing the surface area exposed to direct sun; features all      advantageous for thriving in the new savanna and woodland      environment created as a result of the East African Rift      Valley uplift versus the previous closed forest      habitat.[9][8][10] A new      study provides support for the hypothesis that walking on two      legs, or bipedalism, evolved because it used less energy than      quadrupedal knuckle-walking.[11][12] However, recent studies      suggest that bipedality without the ability to use fire would      not have allowed global dispersal.[13] This      change in gait saw a lengthening of the legs proportionately      when compared to the length of the arms, which were shortened      through the removal of the need for brachiation.      Another change is the shape of the big toe. Recent studies      suggest that Australopithecines still lived part of the time      in trees as a result of maintaining a grasping big toe. This      was progressively lost in Habilines.    <\/p>\n<p>      Anatomically, the evolution of bipedalism has been      accompanied by a large number of      skeletal changes, not just to the legs and pelvis, but      also to the vertebral      column, feet and ankles, and skull.[14] The      femur evolved into a      slightly more angular position to move the center of gravity      toward the geometric center of the body. The knee and ankle      joints became increasingly robust to better support increased      weight. To support the increased weight on each vertebra in      the upright position, the human vertebral column became      S-shaped and the lumbar vertebrae became shorter and      wider. In the feet the big toe moved into alignment with the      other toes to help in forward locomotion. The arms and      forearms shortened relative to the legs making it easier to      run. The foramen magnum migrated under the skull and more      anterior.[15]    <\/p>\n<p>      The most significant changes occurred in the pelvic region,      where the long downward facing iliac blade was shortened and      widened as a requirement for keeping the center of gravity      stable while walking;[16] bipedal      hominids have a shorter but broader, bowl-like pelvis due to      this. A drawback is that the birth canal of bipedal apes is      smaller than in knuckle-walking apes, though there has been a      widening of it in comparison to that of australopithecine and      modern humans, permitting the passage of newborns due to the      increase in cranial size but this is limited to the upper      portion, since further increase can hinder normal bipedal      movement.[17]    <\/p>\n<p>      The shortening of the pelvis and smaller birth canal evolved      as a requirement for bipedalism and had significant effects      on the process of human birth which is much more difficult in      modern humans than in other primates. During human birth,      because of the variation in size of the pelvic region, the      fetal head must be in a transverse position (compared to the      mother) during entry into the birth canal and rotate about 90      degrees upon exit.[18] The      smaller birth canal became a limiting factor to brain size      increases in early humans and prompted a shorter gestation      period leading to the relative immaturity of human offspring,      who are unable to walk much before 12 months and have greater      neoteny, compared      to other primates, who are mobile at a much earlier      age.[10] The      increased brain growth after birth and the increased      dependency of children on mothers had a big effect upon the      female reproductive cycle,[19] and the      more frequent appearance of alloparenting in humans when      compared with other hominids.[20] Delayed      human sexual maturity also led to the evolution of menopause with one      explanation providing that elderly women could better pass on      their genes by taking care of their daughter's offspring, as      compared to having more children of their own.[21]    <\/p>\n<p>      The human species eventually developed a much larger brain      than that of other primatestypically 1,330      cm3 in modern humans, nearly three times the size      of that of a chimpanzee or gorilla.[22] The pattern of      encephalization started with Homo      habilis, after a hiatus with Anamensis and Ardipithecus      species which had smaller brains as a result of their bipedal      locomotion[23] which at approximately      600cm3Homo habilis had a brain      slightly larger than that of chimpanzees, and this evolution      continued with Homo erectus      (8001,100cm3), reaching a maximum in      Neanderthals with an average size of      (1,2001,900cm3), larger even than modern      Homo sapiens. This pattern of brain increase happened      through the pattern of human postnatal brain      growth which differs from that of other apes (heterochrony).      It also allows for extended periods of social learning and language acquisition in juvenile      humans which may have begun 2 million years ago. However, the      differences between the structure of human brains and      those of other apes may be even more significant than      differences in size.[24][25][26][27]    <\/p>\n<p>      The increase in volume over time has affected areas within      the brain unequallythe temporal lobes, which contain centers for      language processing, have increased disproportionately, and      seems to favor a belief that there was evolution after      leaving Africa, as has the prefrontal cortex which has      been related to complex decision-making and moderating social      behavior.[22]      Encephalization has been tied to an increasing emphasis on      meat in the diet,[28][29][30] or with the      development of cooking,[31] and it has been      proposed that intelligence increased as a response to an      increased necessity for solving social problems as human      society became more complex.[32] The human      brain was able to expand because of the changes in the      morphology of smaller mandibles and mandible muscle      attachments to the skull into allowing more room for the      brain to grow.[33]    <\/p>\n<p>      The increase in volume of the neocortex also included a rapid      increase in size of the cerebellum. Traditionally the cerebellum has      been associated with a paleocerebellum and archicerebellum as well as a neocerebellum. Its function has also      traditionally been associated with balance, fine motor      control but more recently speech and cognition. The great apes including humans      and its antecessors had a more pronounced development of the      cerebellum relative to the neocortex than other primates. It      has been suggested that because of its function of      sensory-motor control and assisting in learning complex      muscular action sequences, the cerebellum may have      underpinned the evolution of human's technological      adaptations including the preadaptation of speech.[34][35][36][37]    <\/p>\n<p>      The reason for this encephalization is difficult to discern,      as the major changes from Homo erectus to Homo      heidelbergensis were not associated with major changes in      technology. It has been suggested that the changes have been      associated with social changes, increased empathic      abilities[38][39] and      increases in size of social groupings[40][41][42]    <\/p>\n<p>      The reduced degree of sexual dimorphism is visible primarily      in the reduction of the male canine tooth relative to other ape      species (except gibbons) and reduced brow ridges and general      robustness of males. Another important physiological change      related to sexuality in humans was the evolution of hidden estrus. Humans and bonobos are the only apes      in which the female is fertile year round and in which no      special signals of fertility are produced by the body (such      as genital swelling during estrus).    <\/p>\n<p>      Nonetheless, humans retain a degree of sexual dimorphism in      the distribution of body hair and subcutaneous fat, and in      the overall size, males being around 15% larger than females.      These changes taken together have been interpreted as a      result of an increased emphasis on pair bonding as a possible solution to      the requirement for increased parental investment due to the      prolonged infancy of offspring.    <\/p>\n<p>      The ulnar opposition  the contact between the thumb and the tip of the      little      finger of the same hand  is unique to anatomically modern      humans.[43][44] In      other primates the thumb is short and unable to touch the      little finger.[43] The      ulnar opposition facilitates the precision grip and power      grip of the human hand, underlying all the skilled      manipulations.    <\/p>\n<p>      A number of other changes have also characterized the      evolution of humans, among them an increased importance on      vision rather than smell; a smaller gut; loss of body hair;      evolution of sweat glands; a change in the shape of the      dental arcade from being u-shaped to being parabolic;      development of a chin      (found in Homo sapiens alone); development of styloid processes; and the      development of a descended larynx.    <\/p>\n<p>            -10          <\/p>\n<\/p>\n<p>            -9          <\/p>\n<\/p>\n<p>            -8          <\/p>\n<\/p>\n<p>            -7          <\/p>\n<\/p>\n<p>            -6          <\/p>\n<\/p>\n<p>            -5          <\/p>\n<\/p>\n<p>            -4          <\/p>\n<\/p>\n<p>            -3          <\/p>\n<\/p>\n<p>            -2          <\/p>\n<\/p>\n<p>            -1          <\/p>\n<\/p>\n<p>            0          <\/p>\n<p>            -4500          <\/p>\n<\/p>\n<p>            -4000          <\/p>\n<\/p>\n<p>            -3500          <\/p>\n<\/p>\n<p>            -3000          <\/p>\n<\/p>\n<p>            -2500          <\/p>\n<\/p>\n<p>            -2000          <\/p>\n<\/p>\n<p>            -1500          <\/p>\n<\/p>\n<p>            -1000          <\/p>\n<\/p>\n<p>            -500          <\/p>\n<\/p>\n<p>            0          <\/p>\n<p>      The word homo, the name of the biological genus to      which humans belong, is Latin for \"human\". It was chosen originally by      Carl      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\".[45] Linnaeus      and other scientists of his time also considered the great      apes to be the closest relatives of humans based on morphological and anatomical similarities.    <\/p>\n<p>      The possibility of linking humans with earlier apes by      descent became clear only after 1859 with the publication of      Charles      Darwin's On the Origin of      Species, in which he 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.\"[46]    <\/p>\n<p>      The first debates about the nature of human evolution arose      between Thomas Henry 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 initially agree that the origin of the      mental capacities and the moral sensibilities of humans could      be explained by natural selection, though this later      changed. Darwin applied the theory of evolution and sexual      selection to humans when he published The      Descent of Man in 1871.[47]    <\/p>\n<p>      A major problem at that time was the lack of fossil intermediaries. Neanderthal      remains were discovered in a limestone quarry in 1856, three      years before the publication of On the Origin of      Species, and Neanderthal fossils had been discovered in      Gibraltar even earlier, but it was originally claimed that      these were human remains of a creature suffering some kind of      illness.[48] Despite the 1891 discovery by      Eugne Dubois of what is now called      Homo erectus at Trinil, Java, it was only in the 1920s when such fossils      were discovered in Africa, that intermediate species began to      accumulate.[citation      needed] In 1925, Raymond Dart      described Australopithecus      africanus.[49] The      type      specimen was the Taung Child, an australopithecine infant      which was discovered in a cave. The child's remains were a      remarkably well-preserved tiny skull and an endocast of the brain.    <\/p>\n<p>      Although the brain was small (410cm3), 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 (the hole in the skull      where the spine enters) was evidence of bipedal locomotion. All of these traits      convinced Dart that the Taung Child was a bipedal human      ancestor, a transitional form between apes and humans.    <\/p>\n<p>      During the 1960s and 1970s, hundreds of fossils were found in      East Africa in the regions of the Olduvai Gorge      and Lake      Turkana. The driving force of these searches was the      Leakey family, with Louis Leakey and his wife Mary Leakey, and      later their son Richard and daughter-in-law Meaveall      successful and world-renowned fossil hunters and paleoanthropologists. From the fossil      beds of Olduvai and Lake Turkana they amassed specimens of      the early hominins: the australopithecines and Homo      species, and even Homo erectus.    <\/p>\n<p>      These finds cemented Africa as the cradle of humankind. In      the late 1970s and the 1980s, Ethiopia emerged as the new hot spot of      paleoanthropology after \"Lucy\", the most complete      fossil member of the species Australopithecus      afarensis, was found in 1974 by Donald      Johanson near Hadar in the desertic Afar Triangle      region of northern Ethiopia. Although the specimen had a      small brain, the pelvis and leg bones were almost identical      in function to those of modern humans, showing with certainty      that these hominins had walked erect.[50] Lucy      was classified as a new species, Australopithecus      afarensis, which is thought to be more closely      related to the genus Homo as a direct      ancestor, or as a close relative of an unknown ancestor, than      any other known hominid or hominin from this early time      range; see terms \"hominid\" and \"hominin\".[51] (The specimen was nicknamed      \"Lucy\" after the Beatles' song \"Lucy in the Sky with      Diamonds\", which was played loudly and repeatedly in the      camp during the excavations.[52]) The Afar Triangle      area would later yield discovery of many more hominin      fossils, particularly those uncovered or described by teams      headed by Tim D. White in the 1990s, including      Ardipithecus ramidus and Ardipithecus kadabba.[53]    <\/p>\n<p>      In 2013, fossil skeletons of Homo naledi, an extinct species of hominin assigned      (provisionally) to the genus Homo, were found in the Rising Star      Cave system, a site in South Africa's Cradle of Humankind region in      Gauteng province      near Johannesburg.[54][55] As of September      2015[update],      fossils of at least fifteen individuals, amounting to 1550      specimens, have been excavated from the cave.[55] The species is      characterized by a body mass and stature similar to      small-bodied human populations, a smaller endocranial      volume similar to Australopithecus, and a cranial morphology (skull shape) similar      to early Homo species. The skeletal anatomy combines      primitive features known from australopithecines with features      known from early hominins. The individuals show signs of      having been deliberately disposed of within the cave near the      time of death. The fossils have not yet been dated.[56]    <\/p>\n<p>      The genetic revolution in studies of human evolution started      when Vincent Sarich and Allan Wilson      measured the strength of immunological cross-reactions of      blood      serum albumin      between pairs of creatures, including humans and African apes      (chimpanzees and gorillas).[57] The strength of the      reaction could be expressed numerically as an immunological      distance, which was in turn proportional to the number of      amino acid      differences between homologous proteins in different species.      By constructing a calibration curve of the ID of species'      pairs with known divergence times in the fossil record, the      data could be used as a molecular clock to estimate the      times of divergence of pairs with poorer or unknown fossil      records.    <\/p>\n<p>      In their seminal 1967 paper in Science, Sarich and Wilson      estimated the divergence time of humans and apes as four to      five million years ago,[57] at a time when      standard interpretations of the fossil record gave this      divergence as at least 10 to as much as 30 million years.      Subsequent fossil discoveries, notably \"Lucy\", and      reinterpretation of older fossil materials, notably      Ramapithecus, showed the younger      estimates to be correct and validated the albumin method.    <\/p>\n<p>      Progress in DNA sequencing, specifically mitochondrial DNA (mtDNA) and then      Y-chromosome DNA      (Y-DNA) advanced the understanding of human origins.[58][9][59] Application of the molecular      clock principle revolutionized the study of molecular evolution.    <\/p>\n<p>      On the basis of a separation from the orangutan between 10      and 20 million years ago, earlier studies of the molecular      clock suggested that there were about 76 mutations per      generation that were not inherited by human children from      their parents; this evidence supported the divergence time      between hominins and chimps noted above. However, a 2012      study in Iceland of 78 children and their parents suggests a      mutation rate of only 36 mutations per generation; this datum      extends the separation between humans and chimps to an      earlier period greater than 7 million years ago (Ma).      Additional research with 226 offspring of wild chimp      populations in 8 locations suggests that chimps reproduce at      age 26.5 years, on average; which suggests the human      divergence from chimps occurred between 7 and 13 million      years ago. And these data suggest that Ardipithecus      (4.5 Ma), Orrorin (6 Ma) and Sahelanthropus (7      Ma) all may be on the hominid lineage, and even that the      separation may have occurred outside the East      African Rift region.    <\/p>\n<p>      Furthermore, analysis of the two species' genes in 2006      provides evidence that after human ancestors had started to      diverge from chimpanzees, interspecies mating between      \"proto-human\" and \"proto-chimps\" nonetheless occurred      regularly enough to change certain genes in the new gene pool:    <\/p>\n<p>      The research suggests:    <\/p>\n<p>      In the 1990s, several teams of paleoanthropologists were      working throughout Africa looking for evidence of the      earliest divergence of the hominin lineage from the great      apes. In 1994, Meave Leakey discovered Australopithecus      anamensis. The find was overshadowed by Tim D.      White's 1995 discovery of Ardipithecus ramidus, which      pushed back the fossil record to 4.2 million years ago.    <\/p>\n<p>      In 2000, Martin Pickford and Brigitte Senut      discovered, in the Tugen Hills of Kenya, a 6-million-year-old bipedal hominin which      they named Orrorin      tugenensis. And in 2001, a team led by Michel Brunet discovered      the skull of Sahelanthropus tchadensis which was      dated as 7.2 million      years ago, and which Brunet argued was a bipedal, and      therefore a hominidthat is, a hominin (cf Hominidae;      terms \"hominids\"      and hominins).    <\/p>\n<p>          Different models for the beginning of the present human          species.        <\/p>\n<p>      Anthropologists in the 1980s were divided regarding some      details of reproductive barriers and migratory dispersals of      the Homo genus. Subsequently, genetics has been used      to investigate and resolve these issues. According to the      Sahara pump theory evidence suggests      that genus Homo have migrated out of Africa at least      three and possibly four times (e.g. Homo erectus,      Homo heidelbergensis and two or three times for      Homo sapiens). Recent evidence suggests these      dispersals are closely related to fluctuating periods of      climate change.[63]    <\/p>\n<p>      Recent evidence suggests that humans may have left Africa      half a million years earlier than previously thought. A joint      Franco-Indian team has found human artefacts in the Siwalk      Hills north of New Delhi dating back at least 2.6 million      years. This is earlier than the previous earliest finding of      genus Homo at Dmanisi, in Georgia, dating to 1.85 million      years. Although controversial, tools found at a Chinese cave      strengthen the case that humans used tools as far back as      2.48 million years ago. [64] This      suggests that the Asian \"Chopper\" tool tradition, found in      Java and northern China may have left Africa before the      appearance of the Acheulian hand axe.    <\/p>\n<p>      Up until the genetic evidence became available there were two      dominant models for the dispersal of modern humans. The      multiregional hypothesis      proposed that Homo genus contained only a single      interconnected population as it does today (not separate      species), and that its evolution took place worldwide      continuously over the last couple million years. This model      was proposed in 1988 by Milford H. Wolpoff.[65][66] In contrast the      \"out of Africa\" model proposed that modern H. sapiens      speciated      in Africa recently (that is, approximately 200,000 years ago)      and the subsequent migration through Eurasia resulted in nearly complete      replacement of other Homo species. This model has been      developed by Chris B. Stringer and Peter      Andrews.[67][68]    <\/p>\n<p>      Sequencing mtDNA and Y-DNA sampled from a wide range of      indigenous populations revealed ancestral information      relating to both male and female genetic heritage, and      strengthened the Out of Africa theory and weakened the views      of Multiregional Evolutionism.[69] Aligned in      genetic tree differences were interpreted as supportive of a      recent single origin.[70] Analyses      have shown a greater diversity of DNA patterns throughout      Africa, consistent with the idea that Africa is the ancestral      home of mitochondrial Eve and Y-chromosomal Adam, and that modern      human dispersal out of Africa has only occurred over the last      55,000 years.[71]    <\/p>\n<p>      \"Out of Africa\" has thus gained much support from research      using female mitochondrial DNA and the male Y chromosome.      After analysing genealogy trees constructed using 133 types      of mtDNA, researchers concluded that all were descended from      a female African progenitor, dubbed Mitochondrial Eve. \"Out of Africa\" is      also supported by the fact that mitochondrial genetic      diversity is highest among African populations.[72]    <\/p>\n<p>      A broad study of African genetic diversity, headed by      Sarah      Tishkoff, found the San people had the greatest genetic      diversity among the 113 distinct populations sampled, making      them one of 14 \"ancestral population      clusters\". The research also located a possible origin of      modern human migration in south-western Africa, near the      coastal border of Namibia and Angola.[73] The fossil      evidence was insufficient for archaeologist Richard      Leakey to resolve the debate about exactly where in      Africa modern humans first appeared.[74]      Studies of haplogroups in Y-chromosomal DNA and      mitochondrial DNA      have largely supported a recent African origin.[75] All the evidence from      autosomal DNA also predominantly supports a Recent African      origin. However, evidence for archaic admixture in modern      humans, both in Africa and later, throughout Eurasia has      recently been suggested by a number of studies.[76]    <\/p>\n<p>      Recent sequencing of Neanderthal[77] and      Denisovan[78] genomes shows      that some admixture with these populations has occurred.      Modern humans outside Africa have 24% Neanderthal alleles in their genome,      and some Melanesians have an additional 46% of      Denisovan alleles. These new results do not contradict the      \"out of Africa\" model, except in its strictest      interpretation, although they make the situation more      complex. After recovery from a genetic bottleneck that could      possibly be due to the Toba supervolcano catastrophe,      a fairly small group left Africa and later briefly interbred      on three separate occasions with Neanderthals, probably in      the middle-east, on the Eurasian steppe or even in North      Africa before their departure. Their still predominantly      African descendants spread to populate the world. A fraction      in turn interbred with Denisovans, probably in south-east      Asia, before populating Melanesia.[79]HLA haplotypes of Neanderthal      and Denisova origin have been identified in modern Eurasian      and Oceanian      populations.[80] The      Denisovan EPAS1 gene has also been found in Tibetan      populations.[81]    <\/p>\n<p>      There are still differing theories on whether there was a      single exodus from Africa or several. A multiple dispersal      model involves the Southern Dispersal theory,[82] 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 crossing the Bab el      Mandib to Yemen at a lower sea level 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.[82] This      group seems to have been dependent upon marine resources for      their survival.    <\/p>\n<p>      Stephen Oppenheimer has proposed a      second wave of humans may have later dispersed through the      Persian Gulf oases, and the Zagros mountains into the Middle      East. Alternatively it may have come across the Sinai      Peninsula into Asia, from shortly after 50,000 yrs BP,      resulting in the bulk of the human populations of Eurasia. It      has been suggested that this second group possibly possessed      a more sophisticated \"big game hunting\" 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 each glacial maximum.[82] 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      L3 lineages, which support a single      migration out of Africa that gave rise to all non-African      populations.[83]    <\/p>\n<p>      Stephen Oppenheimer, on the basis of the early date of      Badoshan Iranian Aurignacian, suggests that this second      dispersal, may have occurred with a pluvial period about      50,000 years before the present, with modern human big-game      hunting cultures spreading up the Zagros Mountains, carrying      modern human genomes from Oman, throughout the Persian Gulf,      northward into Armenia and Anatolia, with a variant      travelling south into Israel and to Cyrenicia.[84]    <\/p>\n<p>      The evidence on which scientific accounts of human evolution      are based comes from many fields of natural      science. The main source of knowledge about the      evolutionary process has traditionally been the fossil      record, but since the development of genetics beginning in      the 1970s, DNA analysis has come to occupy a place of      comparable importance. The studies of ontogeny, phylogeny and      especially evolutionary      developmental biology of both vertebrates and      invertebrates offer considerable insight into the evolution      of all life, including how humans evolved. The specific study      of the origin and life of humans is anthropology,      particularly paleoanthropology which focuses on the study of      human prehistory.[85]    <\/p>\n<p>      The closest living relatives of humans are bonobos and      chimpanzees (both genus Pan) and gorillas (genus      Gorilla).[86] With      the sequencing of both the human and chimpanzee genome,      current estimates of the similarity between their DNA      sequences range between 95% and 99%.[86][87][88] By using      the technique called the molecular clock which estimates      the time required for the number of divergent mutations to      accumulate between two lineages, the approximate date for the      split between lineages can be calculated.    <\/p>\n<p>      The gibbons (family Hylobatidae) and then orangutans (genus      Pongo) were the first groups to split from the line      leading to the hominins, including humansfollowed by      gorillas, and, ultimately, by the chimpanzees (genus      Pan). The splitting date between hominin and      chimpanzee lineages is placed by some between 4to8      million years ago,      that is, during the Late Miocene.[4][89][90]Speciation,      however, appears to have been unusually drawn-out. Initial      divergence occurred sometime between 7to13      million years ago,      but ongoing hybridization blurred the separation and delayed      complete separation during several millions of years.      Patterson (2006) dated the final divergence at 5to6      million years      ago.[91]    <\/p>\n<p>      Genetic evidence has also been employed to resolve the      question of whether there was any gene flow      between early modern humans and Neanderthals, and to      enhance our understanding of the early human migration      patterns and splitting dates. By comparing the parts of the      genome that are not under natural selection and which      therefore accumulate mutations at a fairly steady rate, it is      possible to reconstruct a genetic tree incorporating the      entire human species since the last shared ancestor.    <\/p>\n<p>      Each time a certain mutation (Single-nucleotide      polymorphism) appears in an individual and is passed on      to his or her descendants a haplogroup is formed including      all of the descendants of the individual who will also carry      that mutation. By comparing mitochondrial DNA which is      inherited only from the mother, geneticists have concluded      that the last female common ancestor whose genetic marker is      found in all modern humans, the so-called mitochondrial Eve,      must have lived around 200,000 years ago.    <\/p>\n<p>      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.    <\/p>\n<p>      There is little fossil evidence for the divergence of the      gorilla, chimpanzee and hominin lineages.[92] The earliest fossils that have      been proposed as members of the hominin lineage are      Sahelanthropus tchadensis dating from 7 million years ago,      Orrorin tugenensis dating from 5.7 million years ago, and      Ardipithecus kadabba dating to      5.6 million years ago. Each of      these have been argued to be a bipedal ancestor of later      hominins but, in each case, the claims have been contested.      It is also possible that one or more of these species are      ancestors of another branch of African apes, or that they      represent a shared ancestor between hominins and other apes.    <\/p>\n<p>      The question then of the relationship between these early      fossil species and the hominin lineage is still to be      resolved. From these early species, the australopithecines      arose around 4 million years ago and      diverged into robust (also called Paranthropus) and gracile      branches, one of which (possibly A. garhi) probably went on      to become ancestors of the genus Homo. The      australopithecine species that is best represented in the      fossil record is Australopithecus afarensis with more      than one hundred fossil individuals represented, found from      Northern Ethiopia (such as the famous \"Lucy\"), to Kenya, and      South      Africa. Fossils of robust australopithecines such as      Au. robustus (or alternatively Paranthropus robustus) and      Au.\/P. boisei are particularly abundant in South      Africa at sites such as Kromdraai and Swartkrans, and      around Lake      Turkana in Kenya.    <\/p>\n<p>      The earliest member of the genus Homo is Homo      habilis which evolved around 2.8 million years ago.[93]Homo      habilis is the first species for which we have positive      evidence of the use of stone tools. They developed the      Oldowan lithic      technology, named after the Olduvai Gorge in which the first      specimens were found. Some scientists consider Homo      rudolfensis, a larger bodied group of fossils with      similar morphology to the original H. habilis fossils,      to be a separate species while others consider them to be      part of H. habilissimply representing intraspecies      variation, or perhaps even sexual dimorphism. The brains      of these early hominins were about the same size as that of a      chimpanzee, and their main adaptation was bipedalism as an      adaptation to terrestrial living.    <\/p>\n<p>      During the next million years, a process of encephalization      began and, by the arrival (about 1.9 million years ago) of      Homo erectus in the fossil record, cranial capacity      had doubled. Homo erectus were the first of the      hominins to emigrate from Africa, and, from 1.8to1.3      million years ago,      this species spread through Africa, Asia, and Europe. One      population of H. erectus, also sometimes classified as      a separate species Homo ergaster, remained in Africa      and evolved into Homo sapiens. It is believed that      these species, H. erectus and H. ergaster, were      the first to use fire and complex tools.    <\/p>\n<p>      The earliest transitional fossils between H.      ergaster\/erectus and archaic H. sapiens are from      Africa, such as Homo rhodesiensis, but seemingly      transitional forms were also found at Dmanisi, Georgia. These descendants of African      H. erectus spread through Eurasia from ca. 500,000      years ago evolving into H. antecessor, H.      heidelbergensis and H. neanderthalensis. The      earliest fossils of anatomically modern humans      are from the Middle Paleolithic, about 200,000 years ago such      as the Omo      remains of Ethiopia; later fossils from Es Skhul cave in Israel and Southern Europe      begin around 90,000 years ago (0.09      million years      ago).    <\/p>\n<p>      As modern humans spread out from Africa, they encountered      other hominins such as Homo neanderthalensis and the      so-called Denisovans, who may have evolved from populations      of Homo erectus that had left Africa around      2 million years ago. The      nature of interaction between early humans and these sister      species has been a long-standing source of controversy, the      question being whether humans replaced these earlier species      or whether they were in fact similar enough to interbreed, in      which case these earlier populations may have contributed      genetic material to modern humans.[94][95]    <\/p>\n<p>      This migration out of Africa is estimated to have begun about      70,000 years BP (Before Present) and modern humans      subsequently spread globally, replacing earlier hominins      either through competition or hybridization. They inhabited      Eurasia and Oceania by 40,000 years BP, and the Americas by      at least 14,500 years BP.[96]    <\/p>\n<p>      Evolutionary history of the primates can be traced back 65      million years.[97] One of the      oldest known primate-like mammal species, the Plesiadapis,      came from North America;[98] another,      Archicebus, came from China.[99] Other similar      basal primates were widespread in Eurasia and Africa during      the tropical conditions of the Paleocene and Eocene.    <\/p>\n<p>      David R. Begun [100] concluded that      early primates flourished in Eurasia and that a lineage      leading to the African apes and humans, including to      Dryopithecus, migrated south from      Europe or Western Asia into Africa. The surviving tropical      population of primateswhich is seen most completely in the      Upper Eocene and lowermost Oligocene fossil beds of the Faiyum depression southwest      of Cairogave rise to      all extant primate species, including the lemurs of Madagascar,      lorises of Southeast      Asia, galagos or      \"bush babies\" of Africa, and to the anthropoids, which are the Platyrrhines or New World monkeys, the      Catarrhines      or Old World monkeys, and the great apes, including humans      and other hominids.    <\/p>\n<p>      The earliest known catarrhine is Kamoyapithecus from uppermost      Oligocene at Eragaleit in the northern Great Rift Valley in Kenya,      dated to 24 million years ago.[101] Its      ancestry is thought to be species related to Aegyptopithecus, Propliopithecus, and Parapithecus from the Faiyum, at      around 35 million years ago.[102] In 2010,      Saadanius was described as a close      relative of the last common ancestor of the crown      catarrhines, and tentatively dated to 2928 million years      ago, helping to fill an 11-million-year gap in the fossil      record.[103]    <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>More here: <\/p>\n<p><a target=\"_blank\" rel=\"nofollow\" href=\"https:\/\/en.m.wikipedia.org\/wiki\/Human_evolution\" title=\"Human evolution - Wikipedia\">Human evolution - Wikipedia<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Human evolution, also known as hominization, is the evolutionary process that led to the emergence of anatomically modern humans, beginning with the evolutionary history of primates in particular genus Homo and leading to the emergence of Homo sapiens as a distinct species of the hominid family, the great apes.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/evolution\/human-evolution-wikipedia\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":5,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[187748],"tags":[],"class_list":["post-207313","post","type-post","status-publish","format-standard","hentry","category-evolution"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/207313"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=207313"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/207313\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=207313"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=207313"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=207313"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}