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[[Image:Multiregionaltheory.gif|thumb|300px|right|A graph detailing the evolution to modern humans using the Multiregional theory of [[human evolution]]. The horizontal lines represent 'multiregional evolution' gene flow between regional lineages.]]
[[Image:Multiregionaltheory.gif|thumb|300px|right|A graph detailing the evolution to modern humans using the Multiregional theory of [[human evolution]]. The horizontal lines represent 'multiregional evolution' gene flow between regional lineages.]]


'''Multiregional evolution''' is a [[Theory#Theories_as_models|model]] to account for the pattern of [[human evolution]] in the [[Pleistocene]]. The multiregional evolution holds that the [[Human evolution|evolution of humanity]] from the beginning of the [[Pleistocene]] 1.8 million years [[Before Present|BP]] to the present day has been within a single, continuous [[human species]], evolving worldwide from ''[[Homo erectus]]'' to modern ''Homo sapiens''.<ref name=multiregional>{{cite journal
''' ''' is a [[]] . The multiregional holds that the [[Human evolution|evolution of humanity]] from the beginning of the [[Pleistocene]] 1.8 million years [[Before Present|BP]] to the present day has been within a single, continuous [[human species]], evolving worldwide from ''[[Homo erectus]]'' to modern ''Homo sapiens''.<ref name=multiregional>{{cite journal
|last=Wolpoff
|last=Wolpoff
|first=MH
|first=MH
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| pages=206
| pages=206
| url=http://genomebiology.com/2008/9/2/206
| url=http://genomebiology.com/2008/9/2/206
}}</ref> To confuse the current theory with earlier hypothesis some prefer the term '''multiregional hipothesis'''.
}}</ref> To the current theory earlier hypothesis some prefer the term '''multiregional '''.


==History==
==History==

Revision as of 16:19, 30 June 2009

Template:Expert-subject-multiple

A graph detailing the evolution to modern humans using the Multiregional theory of human evolution. The horizontal lines represent 'multiregional evolution' gene flow between regional lineages.

The multiregional hypothesis is a theory of how anatomically modern humans, Homo sapiens sapiens, evolved with a worldwide distribution. The multiregional hypothesis holds that the evolution of humanity from the beginning of the Pleistocene 1.8 million years BP to the present day has been within a single, continuous human species, evolving worldwide from Homo erectus to modern Homo sapiens.[1]

A competing theory of the recent African origin of modern humans (also known as "Out of Africa") has emerged as the near consensus view since the 1990s,[2][3] proposing that modern humans arose in Africa around 100-200,000 years ago, moving out of Africa around 50-60,000 years ago to replace existing human species such as Homo erectus and the Neanderthals.[4]

Proponents of the multiregional hypothesis point to fossil and genomic data^[5] as support for their hypothesis. The gene flow, interbreeding or "admixture" between modern and ancestral human population has not been ruled out,[6][7] although there is not yet any paleogenetic evidence for a contribution from Neanderthals to modern Europeans.[8] To differentiate the current theory from earlier hypothesis some researchers prefer the term multiregional evolution.

History

Weidenreich-Coon

The multiregional hypothesis has its origin in the work of Franz Weidenreich in the 1930s, based on his examination of Peking Man. Weidenreich was an anatomist and observed numerous anatomical characteristics that he thought Peking Man had in common with modern Asians. The Weidenreich Theory stated that human races have evolved independently in the Old World from Homo erectus to Homo sapiens sapiens, while at the same time there was gene flow between the various populations. According to the Weidenreich Theory, genes that were generally adaptive (such as those for intelligence and communication) would flow relatively rapidly from one part of the world to the other, while those that were locally adaptive, would not. A vocal proponent of the Weidenreich theory was Carleton Coon.[9]

Regional continuity

The term "multiregional hypothesis" was first coined in the early 1980s by Milford H. Wolpoff and colleagues as an explanation for the apparent similarities seen in Homo erectus and Homo sapiens fossils from the same region, what they called regional continuity.[10]

Wolpoff rejected the earlier proposal by Coon of parallel evolution,[10] and proposed a theory based on clinal variation that would allow for the necessary balance between local selection and a global species. He proposed that Homo erectus, Neanderthals, Homo sapiens and other humans were a single species. This species arose in Africa two million years ago as H. erectus and then spread out over the world, developing adaptations to regional conditions. It was proposed that for periods of time some populations became isolated, developing in a different direction, but through continuous interbreeding, replacement, genetic drift and selection, adaptations that were an advantage anywhere on earth would spread, keeping the development of the species in the same overall direction, while maintaining adaptations to regional factors. Eventually, the more unusual local varieties of the species would have disappeared in favor of modern humans, retaining some regional adaptations, but with many common features.[10]

Fossil evidence

Some supporters of the multiregional hypothesis, including Wolpoff, argue that fossil evidence is more reliable than estimates based on genetic evidence and molecular clocks, which they contend are subject to genetic drift, bottlenecks and other complicating factors.

Neanderthals

Multiregionalists claimed that the discovery of a possible hybrid Homo sapiens X neanderthalensis fossil child at the Abrigo do Lagar Velho rock-shelter site in Portugal in 1999 further supports the multiregional hypothesis, by reflecting the admixture of diverse human populations[11]. Two other archaeologists dispute this: "the analysis by Duarte et al. of the Lagar Velho child's skeleton is a brave and imaginative interpretation, of which it is unlikely that a majority of paleoanthropologists will consider proven."[12]

In an article appearing in the Proceedings of the National Academy of Sciences[13] in 2007, Erik Trinkaus has brought together the available data, which shows that early modern humans did exhibit evidence of Neandertal traits. "When you look at all of the well dated and diagnostic early modern European fossils, there is a persistent presence of anatomical features that were present among the Neandertals but absent from the earlier African modern humans," Trinkaus said. "Early modern Europeans reflect both their predominant African early modern human ancestry and a substantial degree of admixture between those early modern humans and the indigenous Neandertals."[14]

Peking man

Shang et al see continuity in skeletal remains of archaic people from east Asia.[15]

Early modern humans

Wolpoff and colleagues published an analysis in 2001 of character traits of the skulls of early modern human fossils, which failed to reject a theory of dual ancestry from Javan Homo erectus for Australian early modern humans and Neanderthals for Central European modern humans, and which they said ruled out a replacement model.[16] A subsequent analysis comparing differences of Neanderthal skulls to those of modern humans using 3D morphometric techniques showed a large difference between the two populations, such that Harvatti & al concluded that "we interpret the evidence presented here as supporting the view that Neanderthals represent an extinct human species and therefore refute the regional continuity model for Europe."[17] It has been argued that these differences are consistent with an evolving lineage, as ancestors are never identical to their descendants.[18]

Directly dated EMH

34 Elements of early modern humans (EMH) were unearthed in 2003 in Tianyuan Cave, Zhoukoudian. 14C dated 42-39 ka Tianyuan 1 holotype are oldest, directly dated EMH bones in in eastern Eurasia. Tianyuan 1 exhibits series of typical modern, derived modern human features and few archaic traits, late archaic human traits, such as: large hamulus length, anterior to posterior dental proportions and broad and rounded distal phalangeal tuberosityhis. morphological pattern imply multiregional evolution. [19]

Europe oldest EMH remains are from discovered in 2002 cave Peştera cu Oase near the Iron Gates in the Danubian corridor. Oase 1 holotype revealed specific traits combining a variety of archaic Homo, derived early modern humans, and possibly Neanderthal features. Modern human attributes, classify Oase 1 close to European EMH Late Pleistocene samples. The fossil belongs to the few finds in Europe which could be directly dated and is considered the oldest known early modern human fossil from Europe. Two laboratories independently microfiltrated bone collagen and in colagen dated 14C to 40,500 calendar years.[20] In Europe around 40-30 ka on east-west axis evolved cline between neanderthal traits on west and EMH on east. The human population phenothypical continuity exist in subsequent generations.[20]

Genetic evidence

By analysing haplotype data, Alan Templeton found support for three waves of human migration out of Africa, the first 1.9 million years ago, and concluded that it was impossible that existing Eurasian populations had not interbred with African migrants.[21]

Studies on past population bottlenecks that can be inferred from molecular data have led multiregionalists to conclude that the recent single-origin hypothesis is untenable because there are no population size bottlenecks affecting all genes that are more recent than 2 million years ago.

Proponents of the multiregional hypothesis show genetic sequences of several loci in the human genome with million year old genealogy[35][36][37][38][39][40]. Those data of deep genetic lineages are explained in the multiregional theory framework as a result of heredity from structured ancestral population[41]. The data are not interpreted in light of the RAO hypothesis postulating recent replacement where separated million years ago genetic lineages are at best unpredicted. [42][43]

Researchers

The most prominent current proponents of the multiregional hypothesis are Milford H. Wolpoff, Wu Xinzhi, Alan G. Thorne, James Calcagno[44], John Hawks[45], Alan Templeton, and Erik Trinkaus.

Criticism of the multiregional hypothesis

Multiregional evolution contrasts with the "Recent African Origin" (RAO) theory. According to the latter theory, human evolution was a consequence of many cases of species replacement, as newer species replaced older ones across the human range[citation needed]. Modern human origins, according to the RAO, is the most recent example of species replacement.

In 1997, testing performed on mitochondrial DNA extracted from a Neanderthal skeleton showed modern humans and Neanderthals last shared a common ancestor between 500,000 and 800,000 years ago, and furthermore that all modern humans mtDNA are more closely related to each other than to the Neanderthals mtDNA.[citation needed]

Political implications

Leonard Lieberman and Fatimah Jackson have suggested that any new support for a biological concept of race will likely come from another source, namely, the study of human evolution. They therefore ask what, if any, implications current models of human evolution may have for any biological conception of race.[46]

The major implication for race in the multiregional evolution continuity model involves the time depth of a million or more years in which race differentiation might evolve in diverse ecological regions [...]. This must be balanced[clarification needed] against the degree of gene flow and the transregional operation of natural selection on encephalization due to development of tools and, more broadly, culture.[47]

See also

References

  1. ^ Wolpoff, MH (2000). "Multiregional, not multiple origins". Am J Phys Anthropol. 112 (1): 129–36. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  2. ^ Hua Liu, et al. A Geographically Explicit Genetic Model of Worldwide Human-Settlement History. American Journal of Human Genetics, volume 79 (2006), pages 230–237, quote: Currently available genetic and archaeological evidence is generally interpreted as supportive of a recent single origin of modern humans in East Africa. However, this is where the near consensus on human settlement history ends, and considerable uncertainty clouds any more detailed aspect of human colonization history.
  3. ^ Weaver, Timothy D (2008). "New developments in the genetic evidence for modern human origins". Evolutionary Anthropology: Issues, News, and Reviews. 17 (1). Wiley-Liss: 69–80. doi:10.1002/evan.20161. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  4. ^ Fagundes, NJ (2007). "Statistical evaluation of alternative models of human evolution". Proc Natl Acad Sci U S A. 104 (45): 17614–9. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  5. ^ a b Cox, Mp; Mendez, Fl; Karafet, Tm; Pilkington, Mm; Kingan, Sb; Destro-Bisol, G; Strassmann, Bi; Hammer, Mf (2008). "Testing for archaic hominin admixture on the X chromosome: model likelihoods for the modern human RRM2P4 region from summaries of genealogical topology under the structured coalescent" (Free full text). Genetics. 178 (1): 427–37. doi:10.1534/genetics.107.080432. ISSN 0016-6731. PMC 2206091. PMID 18202385. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  6. ^ Relethford, JH (2008). "Genetic evidence and the modern human origins debate". Heredity. 100 (6). Macmillan: 555–63. doi:10.1038/hdy.2008.14.
  7. ^ Wall, JD (2006). "Archaic admixture in the human genome". Curr Opin Genet Dev. 16 (6): 606–10. doi:10.1016/j.gde.2006.09.006. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  8. ^ Hodgson, JA (2008). "No evidence of a Neanderthal contribution to modern human diversity". Genome Biology. 9 (2). BioMed Central: 206. doi:10.1186/gb-2008-9-2-206. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)CS1 maint: unflagged free DOI (link)
  9. ^ The Races of Europe by Carleton Coon 1939 (Hosted by the Society for Nordish Physical Anthropology)
  10. ^ a b c Wolpoff, MH (1988). "Modern Human Origins". Science. 241 (4867): 772–4. doi:10.1126/science.3136545. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  11. ^ The early Upper Paleolithic human skeleton from the Abrigo do Lagar Velho (Portugal) and modern human emergence in Iberia ;Duarte C, 2. Maurício J, Pettitt P, Souto P, Trinkaus E, van der Plicht H, Zilhão J (1999) Proc Natl Acad Sci USA 96:7604–7609,[1]
  12. ^ Chunky Gravettian child; Ian Tattersall and Jeffrey H. Schwartz .[2]
  13. ^ Trinkaus, E (2007). "European early modern humans and the fate of the Neandertals" (Free full text). Proceedings of the National Academy of Sciences of the United States of America. 104 (18): 7367–72. doi:10.1073/pnas.0702214104. ISSN 0027-8424. PMC 1863481. PMID 17452632. {{cite journal}}: Unknown parameter |month= ignored (help)
  14. ^ http://www.sciencedaily.com/releases/2007/04/070423185434.htm The Emerging Fate Of The Neandertals
  15. ^ Shang; et al. (1999). "An early modern human from Tianyuan Cave, Zhoukoudian, China". Proceedings of the National Academy of Sciences. 104 (16): 6573. doi:10.1073/pnas.0702169104. PMID 17416672. {{cite journal}}: Explicit use of et al. in: |author= (help)
  16. ^ Wolpoff, Milford H (2001). "Modern Human Ancestry at the Peripheries: A Test of the Replacement Theory". Science. 291. AAAS: 293–297. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  17. ^ Harvati, Katerina (2004). "Neanderthal taxonomy reconsidered: Implications of 3D primate models of intra- and interspecific differences". PNAS. 101 (5): 1147–1152. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  18. ^ Wolpoff, Milford (2004). "Why not the Neandertals?" (PDF). World Archaeology. 36: 527. doi:10.1080/0043824042000303700. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  19. ^ Shang, H; Tong, H; Zhang, S; Chen, F; Trinkaus, E (2007). "An early modern human from Tianyuan Cave, Zhoukoudian, China" (Free full text). Proceedings of the National Academy of Sciences of the United States of America. 104 (16): 6573–8. doi:10.1073/pnas.0702169104. ISSN 0027-8424. PMC 1871827. PMID 17416672. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  20. ^ a b Trinkaus, E; Moldovan, O; Milota, S; Bîlgăr, A; Sarcina, L; Athreya, S; Bailey, Se; Rodrigo, R; Mircea, G; Higham, T; Ramsey, Cb; Van, Der, Plicht, J (2003). "An early modern human from the Peştera cu Oase, Romania" (Free full text). Proceedings of the National Academy of Sciences of the United States of America. 100 (20): 11231–6. doi:10.1073/pnas.2035108100. ISSN 0027-8424. PMC 208740. PMID 14504393. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  21. ^ Williams, Robyn (2004). "Are We Neanderthals?". The Science Show. ABC Radio. Retrieved 2009-05-30.
  22. ^ Evans, Pd; Mekel-Bobrov, N; Vallender, Ej; Hudson, Rr; Lahn, Bt (2006). "Evidence that the adaptive allele of the brain size gene microcephalin introgressed into Homo sapiens from an archaic Homo lineage" (Free full text). Proceedings of the National Academy of Sciences of the United States of America. 103 (48): 18178–83. doi:10.1073/pnas.0606966103. ISSN 0027-8424. PMC 1635020. PMID 17090677. ... As such, microcephalin shows by far the most compelling evidence of admixture among the human loci examined thus far. Speculation about the identity of the archaic Homo population from which the microcephalin D allele introgressed into the modern human gene pool points to the Neanderthal lineage as a potential (although by no means only) candidate. Anatomically modern humans and Neanderthals shared a long period of coexistence, from as early as 130,000 years ago in the Middle East (39) to as late as 35,000 years ago in Europe (40), consistent with the estimated introgression time of the microcephalin D allele at or sometime before (approx)37,000 years ago. Furthermore, the worldwide frequency distribution of the D allele, exceptionally high outside of Africa but low in sub-Saharan Africa (29), suggests, but does not necessitate, admixture with an archaic Eurasian population. ... {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  23. ^ Trinkaus, E (2007). "European early modern humans and the fate of the Neandertals" (Free full text). Proceedings of the National Academy of Sciences of the United States of America. 104 (18): 7367–72. doi:10.1073/pnas.0702214104. ISSN 0027-8424. PMC 1863481. PMID 17452632. {{cite journal}}: Unknown parameter |month= ignored (help)
  24. ^ Evans, Pd; Gilbert, Sl; Mekel-Bobrov, N; Vallender, Ej; Anderson, Jr; Vaez-Azizi, Lm; Tishkoff, Sa; Hudson, Rr; Lahn, Bt (2005). "Microcephalin, a gene regulating brain size, continues to evolve adaptively in humans". Science (New York, N.Y.). 309 (5741): 1717–20. doi:10.1126/science.1113722. ISSN 0036-8075. PMID 16151009. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  25. ^ sequence and gene tree for RRM2P4 haplotypes oxfordjournals.org
  26. ^ Garrigan, D; Mobasher, Z; Severson, T; Wilder, Ja; Hammer, Mf (2005). "Evidence for archaic Asian ancestry on the human X chromosome" (Free full text). Molecular biology and evolution. 22 (2): 189–92. doi:10.1093/molbev/msi013. ISSN 0737-4038. PMID 15483323. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  27. ^ Rosalind M. Harding (March 16, 1999). "More on the X files". Proceedings of the National Academy of Sciences (6): 2582–2584. the pattern of diversity at the PDHA1 locus unexpected is that this extreme structure is observed in a polymorphism with an estimated total coalescent-time depth of 1.86 million years {{cite journal}}: Unknown parameter |vol= ignored (|volume= suggested) (help)
  28. ^ Garrigan, D; Mobasher, Z; Severson, T; Wilder, Ja; Hammer, Mf (2005). "Evidence for archaic Asian ancestry on the human X chromosome" (Free full text). Molecular biology and evolution. 22 (2): 189–92. doi:10.1093/molbev/msi013. ISSN 0737-4038. PMID 15483323. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  29. ^ Harris, E. E. ;Jody Hey (1999). [pdf "X chromosome evidence for ancient human histories"]. Proceedings of the National Academy of Sciences. 96: 3320. doi:10.1073/pnas.96.6.3320. {{cite journal}}: Check |url= value (help)CS1 maint: multiple names: authors list (link)
  30. ^ J. Hardy, A. Pittman, A. Myers, K. Gwinn-Hardy, H.C. Fung, R. de Silva, M. Hutton and J. Duckworth (2005). "Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens". Biochemical Society Transactions. 33, part 4, . {{cite journal}}: Unknown parameter |qoute= ignored (help)CS1 maint: extra punctuation (link) CS1 maint: multiple names: authors list (link)
  31. ^ Shaw-Smith, C; Pittman, Am; Willatt, L; Martin, H; Rickman, L; Gribble, S; Curley, R; Cumming, S; Dunn, C; Kalaitzopoulos, D; Porter, K; Prigmore, E; Krepischi-Santos, Ac; Varela, Mc; Koiffmann, Cp; Lees, Aj; Rosenberg, C; Firth, Hv; De, Silva, R; Carter, Np (2006). "Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability". Nature genetics. 38 (9): 1032–7. doi:10.1038/ng1858. ISSN 1061-4036. PMID 16906163. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  32. ^ Zody, Mc; Jiang, Z; Fung, Hc; Antonacci, F; Hillier, Lw; Cardone, Mf; Graves, Ta; Kidd, Jm; Cheng, Z; Abouelleil, A; Chen, L; Wallis, J; Glasscock, J; Wilson, Rk; Reily, Ad; Duckworth, J; Ventura, M; Hardy, J; Warren, Wc; Eichler, Ee (2008). "Evolutionary toggling of the MAPT 17q21.31 inversion region". Nature genetics. doi:10.1038/ng.193. ISSN 1061-4036. PMID 18690220. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  33. ^ Introgression and microcephalin FAQ John Hawks [3]
  34. ^ Almos, Pz; Horváth, S; Czibula, A; Raskó, I; Sipos, B; Bihari, P; Béres, J; Juhász, A; Janka, Z; Kálmán, J (2008). "H1 tau haplotype-related genomic variation at 17q21.3 as an Asian heritage of the European Gypsy population". Heredity. 101 (5): 416–9. doi:10.1038/hdy.2008.70. ISSN 0018-067X. PMID 18648385. {{cite journal}}: Unknown parameter |month= ignored (help); Unknown parameter |qoute= ignored (help)CS1 maint: multiple names: authors list (link)
  35. ^ Evidence for Archaic Asian Ancestry on the Human X Chromosome; Daniel Garrigan, Zahra Mobasher, Tesa Severson, Jason A. Wilder and Michael F. Hammer; Molecular Biology and Evolution 2005 22(2):189-192; doi:10.1093/molbev/msi013 [4]
  36. ^ Deep Haplotype Divergence and Long-Range Linkage Disequilibrium at Xp21.1 Provide Evidence That Humans Descend From a Structured Ancestral Population; Daniel Garrigan, Zahra Mobasher, Sarah B. Kingan, Jason A. Wilder and Michael F. Hammer; Genetics, Vol. 170, 1849-1856, August 2005, Copyright © 2005 doi:10.1534/genetics.105.041095 [5]
  37. ^ X chromosome evidence for ancient human histories; Eugene E. Harris and Jody Hey; PNAS March 16, 1999 vol. 96 no. 6 3320-3324 [6]
  38. ^ A common inversion under selection in Europeans; Stefansson H, Helgason A, Thorleifsson G, Steinthorsdottir V, Masson G, Barnard J, Baker A, Jonasdottir A, Ingason A, Gudnadottir VG, et al. Nature Genetics 37, 129 - 137 (2005) Published online: 16 January 2005; doi:10.1038/ng1508
  39. ^ Evidence that the adaptive allele of the brain size gene microcephalin introgressed into Homo sapiens from an archaic Homo lineage; Patrick D. Evans, Nitzan Mekel-Bobrov, Eric J. Vallender, Richard R. Hudson and Bruce T. Lahn; PNAS November 28, 2006 vol. 103 no. 48 18178-18183 [7]
  40. ^ Early modern human diversity suggests subdivided population structure and a complex out-of-Africa scenario Philipp Gunza, Fred L. Booksteina, Philipp Mitteroeckera, Andrea Stadlmayra, Horst Seidlera and Gerhard W. Webera; 10.1073/pnas.0808160106 [8]
  41. ^ [9]
  42. ^ Ancient lineages in the genome: A response to Fagundes et al; Daniel Garrigan and Michael F. Hammer; doi:10.1534/genetics.105.041095 [10]
  43. ^ Reply to Garrigan and Hammer: Ancient lineages and assimilation; Nelson J. R. Fagundes, Nicolas Ray, Mark Beaumont, Samuel Neuenschwande, Francisco M. Salzano†, Sandro L. Bonatto and Laurent Excoffier ;10.1073/pnas.0711261105 [11] qoute:We must repeat that our results do not exclude the occurrence of some admixture events between modern and archaic humans,
  44. ^ Calcagno homepage link
  45. ^ John Hawks homepage link
  46. ^ Leonard Lieberman and Fatimah Linda C. Jackson (1995) "Race and Three Models of Human Origin" in ­American Anthropologist Vol. 97, No. 2, pp. 232-234
  47. ^ Leonard Lieberman and Fatimah Linda C. Jackson (1995) "Race and Three Models of Human Origin" in ­American Anthropologist Vol. 97, No. 2, pp. 237

Reviews

  • Templeton, AR (2002). "Out of Africa again and again". Nature. 416: 45–51.
  • Pearson, Osbjorn M (2004). "Has the Combination of Genetic and Fossil Evidence Solved the Riddle of Modern Human Origins?". Evolutionary Anthropology. 13: 145–159.
  • Adams, J (2008). "Human Evolutionary Tree". Nature Education. 1 (1). Macmillian.
  • Johanson, Donald C (May 2001). "Origins of Modern Humans: Multiregional or Out of Africa?". ActionBioscience. Retrieved 2009-05-30.
  • [12] - 'Genomics refutes an exclusively African origin of humans' (pdf) Vinayak Eswaran, Henry Harpending, Alan R. Rogers, Journal of Human Evolution (2005)
  • [13] - 'Templeton tree'
  • [14] - 'The Hybrid Child from Portugal'
  • Biochem. Soc. Trans (2005) 33, 582-585 - J. Hardy and others - Molecular Mechanisms of Neurodegeneration (Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens)
  • Kent Holsinger's web site - 'Drift and migration' (only 1 migrant per generation between populations of reasonable big sizes can prevent divergence in allelic frequencies)
  • Genetics - 'Deep Haplotype Divergence and Long-Range Linkage Disequilibrium at Xp21.1 Provide Evidence That Humans Descend From a Structured Ancestral Population' (first genetic evidence that statistically rejects the null hypothesis that our species descends from a single, historically panmictic population), Daniel Garrigan, Zahra Mobasher, Sarah B. Kingan, Jason A. Wilder, and Michael F. Hammer, University of Arizona, Tucson, Genetics, Vol. 170, 1849-1856, August 2005
  • Linfield.edu - 'The Origin of Modern Humans: Multiregional and Replacement Theories', Michael Roberts, Linfield College
  • [15] - 'Evidence for Archaic Asian Ancestry on the Human X Chromosome' (suggests ancient RRM2P4 lineage is remnant of introgressive hybrid of anatomically modern humans from Africa and archaic populations in Eurasia), Daniel Garrigan, Zahra Mobasher, Tesa Severson, Jason A. Wilder, Michael F. Hammer, University of Arizona, Tucson, Molecular Biology and Evolution, vol 22, no 2, p 189–192 (2005)
  • PNAS.org - 'Mitochondrial DNA sequences in ancient Australians: Implications for modern human origins', Gregory J. Adcock, Elizabeth S. Dennis, Simon Easteal, Gavin A. Huttley, Lars S. Jermiin, W. James Peacock, Alan Thorne, Australian National University, Proceedings of the National Academy of Sciences, vol 98, no 2, p 537-542 (January 16, 2001)
  • StephenJayGould.org - 'Out of Africa vs. Multiregionalism', Tod Billings (December 7, 1999)
  • TalkOrigins.org - 'The evolution of modern humans: where are we now?' Christopher B. Stringer, General Anthropology, vol 7, no 2, p 1–5 (2001)
  • Selection, nuclear genetic variation, and mtDNA