The unidirectional phylogeny of Homo sapiens anchors the origin of modern humans in Eurasia | Hereditas

The out of Eurasia phylogeny

Figure 1 outlines basal Hs relationships in accordance with recent advances in Eurasian palaeontology and phylogenetics [1]. The Eurasian-derived parts of the figure are marked blue and the African contribution red. Homo erectus, He, has been placed at the root of the tree consistent with He entering Eurasia from Africa > 2 million years ago [15] in agreement with the Eurasian palaeontology of the species. As apparent the evolution is continuous and unidirectional through the entire tree from the oldest to the most recent Hss divergence as represented by the African Mbuti/San and the Eurasian Lund.

The nuDNA phylogeny leading to Hss, Homo sapiens sapiens. Blue: Eurasian lineages. Red: African lineages. H. erectus has been placed at the root of the tree in accordance with the artefact sequence related to the Eurasian existence of He 2,12 MYBP [15]. The divergence between Hs, H. sapiens, and Ha, H. antecessor, has been dated to ≈ 850,000 YBP [16, 17], that between Hss and Hsn, H. s. neanderthalensis, to ≈ 800,000 YBP and that between Lund and Mbuti/San to ≈ 250,000 YBP. Hsn divides into Hsnn, Neanderthals proper, and Hsnd, Denisova, with Hsnn dividing further into SH-Hsnn (Hsnn at Sima de los Huesos) and Hsnn*, a branch arising as the result of the mtDNA introgression that took place from Hss into Hsnn* ≈ 500,000 YBP [1]

The earliest divergence in Fig. 1, that between Ha, Homo antecessor, and Hs, Homo sapiens, has been placed palaeontologically [16] and molecularly [17] at ≈ 850,000 YBP. As Fig. 1 shows, the Hs branch splits into a branch leading to extant humans, Hss, and another branch, Hsn, H. sapiens neanderthalensis, that gave rise to Hsnn, Neanderthals proper, and Hsnd, Denisovans. Hsnn diverged early into two branches, SH-Hsnn and Hsnn*, both palaeontologically and molecularly [18] identified. SH-Hsnn inhabited northern Spain, while Hsnn* reigned both in Europe and Asia, as established by extensive Eurasian fossil finds.

The arrowheads that lead from Hss to Hsnn* in Fig. 1 mark the phylogeny resulting from the mtDNA introgression that took place from Hss into Hsnn* ≈ 500,000 YBP [1 As shown in Fig. 2 the introgression joins Hss and Hsnn* on a common mtDNA branch, therewith restricting the initial mtDNA branch of Hsn to SH-Hsnn and Hsnd. With the Neanderthals strictly limited to Eurasia it becomes apparent that the mtDNA introgression from Hss to Hsnn* could only take place in conjunction with the contemporary coexistence of both Hss and Hsnn in Eurasia [1, 6], a circumstance that invalidates OOAH since that hypothesis does not allow the existence of Hss in Eurasia at the time in question.

The mtDNA relationships of Hs demonstrating the paraphyly of the African Hss populations as resolved by PPA. Blue: non-African taxa; red: African taxa. Hsnn*: Hsnn other than SH-Hsnn. The arrowheads signify the mtDNA introgression that gave rise to Hsnn*. The limitation of Hsnn to Eurasia places the mtDNA introgression in this continent, reversing the direction of Hss evolution behind OOAH. The Hss part of the tree underlines the phylogenetic continuity among non-African populations and the paraphyly of the African populations including the two Yoruba [1]. AuAb: Australian aborigines; PNG: Papua New Guinean; Han: Chinese; Lund: The first described non-chimaeric human mtDNA molecule [19]; French: A European, as representing previous genomic findings [20]

An extensive genomic study of extant humans that was presented a few years ago [20] identified a basal Hss divergence between a Eurasian (French) genome and the genome of the African Mbuti, but the significance of the finding for addressing Hss origin and evolution was not discussed. However, as maintained subsequently on phylogenetic grounds [6], this basal Hss divergence compromised OOAH since that hypothesis rested instead upon an Hss exodus out of Africa into Eurasia by a late arising African population and not on a population that constituted the earliest divergence among recent humans.

In the recent study by Árnason and Hallström [1] the direction of evolution in the Hss tree was established by applying a new approach, Progressive Phylogenetic Analysis, PPA, which demonstrated that the African populations constituted a paraphyletic grouping. The African paraphyly invalidated the postulate of an Hss origin in Africa and a late exodus out of that continent into Eurasia since the PPA identified instead a minimum of three separate waves of Hss migration from Eurasia into Africa the earliest being that of the ancestors of Mbuti/San. Thus, in contradiction to OOAH the PPA approach yielded results that were consistent with a continuous unidirectional Eurasian evolution on the Hs branch from the divergence between H. antecessor and H. sapiens to the apical tips of extant Hss as demonstrated in Figs. 1 and 2.

The profiles of the Y-DNA and mtDNA phylogenies of Hss

Figure 3a–c shows the phylogenetic relationships of recent Hss as resolved in analysis of two separate sets of data, the paternally transmitted Y-DNA and the maternally transmitted mtDNA. The Y-DNA tree of OOEH [3, 4] is shown to the left in the figure, the mtDNA tree of OOEH in the middle [1] and the commonly acknowledged Y-DNA tree of OOAH (e.g. [2]) to the right. Although the three trees are superficially similar they are fundamentally different in that trees 3a and 3b are consistent with the out of Eurasia hypothesis whereas tree 3c is that of OOAH.

The Y-DNA and mtDNA phylogenies of Hss with the Y-DNA tree (a) [4] and the mtDNA tree (b) [1] representing the OOEH phylogeny, and tree (c) standing for the OOAH phylogeny of both mtDNA and Y-DNA. Trees (a) and (b) are consistent with a residing Eurasian Hss populations and a series of Hss exoduses from Eurasia into Africa. Position A00 in the Y-DNA tree and the corresponding position in the mtDNA tree mark the position at which the basal African and non-African lineages of extant Hss populations coalesce. Position β in tree (a) signifies the beginning of the Eurasian diversification of Hss dated to ≈ 125,000 to 120,000 YBP in the mtDNA tree [1]. The blue branch in (c) signifies a late Hss exodus out of Africa as assumed by the out of Africa hypothesis. As underlined in Figs. 1 and 2, the position of the root of the phylogeny in tree (c) is without connection to the Eurasian evolution of Hss and Hsn(Hsnn + Hsnd)

The extensive Y-DNA study [4] behind Fig. 3a showed a minimum of five waves of Hss migration from Eurasia into Africa while the more limited mtDNA sampling behind 3b [1] identified a minimum of three migrations with each of these coinciding with the Y-DNA results, consistent with the presence of both males (Y-DNA) and females (mtDNA) in each population migrating into Africa. As apparent a divergence between Mbuti and San prior to their migration into Africa [5] would raise the number of waves into Africa by one, as would also any migration connected to the B + C branch [4] that has been tentatively indicated on the mtDNA tree.

With respect to the phylogeny in Fig. 3c it should be noted that the OOAH tree and the out of Africa hypothesis, in addition to their earlier rebuttal [3, 4], became rejected by the recent PPA findings [1] which demonstrated the paraphyly of the African populations. In contradiction to OOAH these molecular results were all in accordance with the out of Eurasia hypothesis and the Eurasian palaeontology of both Hss and Hsn(Hsnn + Hsnd), a topic that has been largely ignored by the adherents of OOAH.

The Y-DNA tree in Fig. 3a and the mtDNA tree in 3b are both consistent with a unidirectional Hss evolution from the Eurasian root of the Hs tree to the tip of each individual Hss branch. The Y-DNA tree is based upon the largest sample that has been used to delineate the Y-DNA relationships of extant humans. The analysis [4] identified a Eurasian Y-DNA coalescence, A00, that was followed by three separate Hss exoduses, A0, A and α, from Eurasia into Africa with A0 signifying the earliest and α the most recent of these early exoduses. The Eurasian Y-DNA phylogeny shows a continuous Eurasian span from position α to the extensive Eurasian diversification beginning at position β in the Y-DNA tree.

The mtDNA tree in Fig. 3b mirrors the Y-DNA phylogeny in accordance with a shared identity, male and female, within each pair of the Hss exoduses from Eurasia into Africa. Similarly the barren Eurasian branch between the last exodus into Africa, and position β, the initiation of the Eurasian diversification of Hss is common to both phylogenies although the span is longer in the Y-DNA phylogeny than in the mtDNA tree, a distinction that might be related to different modes of calculation.

The phylogenetic position at position β in the Y-DNA tree was discussed in the recent mtDNA study [1] in the context of climatic cycles, the most severe of these ending ≈ 125,000 YBP. This climatic circumstance coincides with the restricted molecular variation at the corresponding position in the Eurasian phylogeny prior to the striking population expansion occurring later in the two separate sets of molecular data behind the Y-DNA and mtDNA phylogenies.