On the Number of Ancestral Human Species

The number of species within the human evolutionary tree remains a major point of debate. Genomic distances for living humans and other apes may be used to estimate hominin diversity and therefore to set boundaries for palaeontological scenarios. A minimum of five species is recognizable but scenarios involving much higher estimates of diversity cannot be ruled out.

Keywords: hominin evolution; species; diversity; genetics

Figure 1. Lower Pleistocene hominin crania from the ‘Hanging Remnant’ unit of Member 1 of the Swartkrans Cave (South Africa). Specimen SK 847 (above) is commonly classified in Homo erectus and SK 48 (below) in Paranthropus robustus. According to the single species model, both would be assigned along with living humans to H. sapiens.
Figure 2. Genetic distances between humans, chimpanzees and the human–chimpanzee last common ancestor (HC-LCA). The distances between humans and the HC-LCA, and between chimpanzees and the HC-LCA, are corrected for a rate slow-down in the last 1 million years of the human lineage (see text).
Figure 3. Number of species in the direct lineage to modern humans estimated from genetic distances. Assuming a speciation model of cladogenesis, each time a new species arises within the direct lineage, bifurcation leads to the origin of a second (sister) species. Under this model, diversity within the hominin clade would be estimated at five species. (Note: white arrows represent the direct lineage to modern humans.)
Figure 4. Species lineages identified in the present study are approximately equivalent to five of the major genera used for the hominin clade.
Figure 5. Alternative scenario of species diversity in the hominin clade. Some of the assumptions and criteria used earlier have been relaxed. This estimate is close to reaching the maximum number of species that can be inferred using a genetic yardstick.
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 References
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 Further Reading
    Ackermann RR (2002) Patterns of covariation in the hominoid craniofacial skeleton: implications for paleoanthropological models. Journal of Human Evolution 42: 167–187.
    Ackermann RR and Cheverud JM (2004) Detecting genetic drift versus selection in human evolution. Proceedings of the National Academy of Sciences of the USA 101: 17946–17951.
    Conroy GC (2002) Speciosity in the early Homo lineage: too many, too few, or just about right? Journal of Human Evolution 43: 759–766.
    Curnoe D and Thorne A (2003) Number of ancestral human species: a molecular perspective. Homo–Journal of Comparative Human Biology 53: 201–224.
    Foley R (2002) Adaptive radiations and dispersals in hominin evolutionary ecology. Evolutionary Anthropology 9(Suppl. 1): 32–37.
    Hlusko LJ (2004) Integrating the genotype and phenotype in hominid paleontology. Proceedings of the National Academy of Sciences of the USA 101: 2653–2657.
    book Kimbel WH and Rak Y (1993) "The importance of species taxa in palaeoanthropology and an argument for the phylogenetic concept of the species category". In: Kimbel WH and Martin LB (eds) Species, Species Concepts, and Primate Evolution, pp. 461–484. New York: Plenum Press.
    Scott JE and Lockwood CA (2004) Patterns of tooth crown size and shape variation in great apes and humans and species recognition in the hominid fossil record. American Journal of Physical Anthropology 125: 303–319.
    White T (2003) Early hominids-diversity or distortion? Science 299: 1994–1997.
    book Wolpoff MH (1996) Human Evolution. New York: Knopf.
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How to Cite close
Curnoe, Darren(Mar 2008) On the Number of Ancestral Human Species. In: eLS. John Wiley & Sons Ltd, Chichester. http://www.els.net [doi: 10.1002/9780470015902.a0020814]