Book contents
- Frontmatter
- Contents
- List of Contributors
- Acknowledgements: The European Science Foundation
- PART I: Chronology and environment
- PART II: Methods and phylogeny
- 3 Computer-assisted morphometry of hominoid fossils: the role of morphometric maps
- 4 Comparative analysis of the iliac trabecular architecture in extant and fossil primates by means of digital image processing techniques: implications for the reconstruction of fossil locomotor behaviours
- 5 Dental microwear and diet in Eurasian Miocene catarrhines
- 6 How reliable are current estimates of fossil catarrhine phylogeny? An assessment using extant great apes and Old World monkeys
- 7 Cranial discrete variation in the great apes: new prospects in palaeoprimatology
- PART III Miocone hominoids: function and phylogeny
- Index
6 - How reliable are current estimates of fossil catarrhine phylogeny? An assessment using extant great apes and Old World monkeys
from PART II: Methods and phylogeny
Published online by Cambridge University Press: 06 January 2010
- Frontmatter
- Contents
- List of Contributors
- Acknowledgements: The European Science Foundation
- PART I: Chronology and environment
- PART II: Methods and phylogeny
- 3 Computer-assisted morphometry of hominoid fossils: the role of morphometric maps
- 4 Comparative analysis of the iliac trabecular architecture in extant and fossil primates by means of digital image processing techniques: implications for the reconstruction of fossil locomotor behaviours
- 5 Dental microwear and diet in Eurasian Miocene catarrhines
- 6 How reliable are current estimates of fossil catarrhine phylogeny? An assessment using extant great apes and Old World monkeys
- 7 Cranial discrete variation in the great apes: new prospects in palaeoprimatology
- PART III Miocone hominoids: function and phylogeny
- Index
Summary
Introduction
Cladistic analysis has been used for more than 20 years to reconstruct the phylogenetic relationships of fossil catarrhine species and genera (e.g. Delson & Andrews, 1975; Eldredge & Tattersall, 1975; Delson, 1977; Delson et al., 1977; Tattersall & Eldredge, 1977; Andrews, 1978, 1992; Corruccini & McHenry, 1980; Harrison, 1982; Skelton & McHenry, 1986; Wood & Chamberlain, 1986, 1987; Andrews & Martin, 1987; Chamberlain & Wood, 1987; Strasser & Delson, 1987; Stringer, 1987; Wood, 1988, 1991, 1992; Skelton & McHenry, 1992; Lieberman et al., 1996; Begun et al., 1997; Cameron, 1997; Rae, 1997; Strait et al., 1997). However, it is now apparent that, in contrast to the situation with higher-level primate taxa (Harrison, 1993), few of the relationships supported by these analyses can be considered to be reliable. This is demonstrated by the small increases in length required to alter the topologies of the most parsimonious cladograms. For example, the addition of only one step converts the Homo monophyly seen in Wood's (1991) most parsimonious cladogram into Homo paraphyly, as well as altering the relationships of A. africanus (Wood, 1992). Likewise, the addition of two steps to the cladogram preferred by Strait et al. (1997) results in Homo paraphyly (Wood & Collard, 1999). These examples are taken from the hominin palaeontological literature, but they could easily have been taken from studies of Miocene hominoids, Eurasian pliopithecids, or fossil Old World monkeys (e.g. Harrison, 1993; Rae, 1997). The unreliability of the most parsimonious cladograms is also illustrated by the results of Corruccini's (1994) bootstrap re-analysis of hominin data from Wood & Chamberlain (1986), Skelton et al. (1986), Chamberlain & Wood (1987) and Skelton & McHenry (1992).
- Type
- Chapter
- Information
- Hominoid Evolution and Climatic Change in EuropePhylogeny of the Neogene Hominoid Primates of Eurasia, pp. 118 - 150Publisher: Cambridge University PressPrint publication year: 2001
- 8
- Cited by