Table 3.
Taxon | Alternative hypothesis* | Δ length | References |
---|---|---|---|
Palaeognathae | ∪ Galloanseromorphae | 54 | Sibley & Ahlquist (1990) |
Ratitae (global)† | Δ topology | 31 | Cracraft (1974a) |
Ratitae (local)† | Δ topology | 63 | Cracraft (1974a) |
Δ topology‡ | 17 | Cooper et al. (2001) | |
Δ topology‡ | 13 | Haddrath & Baker (2001) | |
Galloanserimorphae | Polyphyly§ | [19] | Bourdon et al. (2005) |
Galliformes | Polyphyly | 90 | Dyke et al. (2003) |
Megapodiidae | ∪ Cracidae | 10 | Dyke et al. (2003) |
Meleagrididae | ∪ Phasianidae | 20 | Dyke et al. (2003) |
Anseriformes | Δ familial topology | 54 | Olson & Feduccia (1980a); Livezey (1997a) |
Anhimae | ∪∨⊂ Galliformes | 41 | Olson & Feduccia (1980a); Livezey (1997a) |
Gaviomorphae | ∪ Charadriomorphae | 72 | Storer (1956); Olson (1985) |
Podicipediformes | ∪ Phoenicopteridae | 146 | Mayr & Clarke (2003); Mayr (2004a) |
∪ Charadriomorphae | 54 | Storer (1956) | |
∪ Eurypygidae | 182 | Zusi & Storer (1969) | |
∪ Ralliformes | 159 | Olson (1985); Houde (1994) | |
Pelecaniformes | Δ topology | 344 | Kennedy & Spencer (2004: fig. 1B) |
Sulae | Δ topology | 125 | Kennedy et al. (2005: fig. 8) |
Balaenicepitidae | ¬∪ Pelecaniformes | 30 | Cracraft (1985); Mayr (2003a) |
Scopidae | ∪∨⊂ Pelecaniformes | 23 | Mayr (2003a) |
Threskiornithidae | ∪∨⊂ Charadriiformes | 174 | Olson (1978) |
Ardeidae | ⊂ (Turnices ∪ Eurypygae) | 75 | Olson (1978) |
Phoenicopteridae | ∪ Anseriformes | 107 | Feduccia (1976, 1977b); Hagey et al. (1990) |
∪ Cladorhynchini | 154 | Olson & Feduccia (1980b) | |
Gruiformes (traditional) | Monophyly¶ | 11 | Livezey (1998b) |
Charadriiformes | Δ topology | 60 | Strauch (1978) fideChu (1995: fig. 1) |
Δ topology | 106 | Sibley & Ahlquist (1990) fidePaton et al. (2003) | |
Δ topology | 82 | Chu (1995: fig. 8), excluding Ibidorhyncha | |
Mesitornithidae | ∪ Cuculiformes | 107 | Mayr & Ericson (2004) |
Strigiformes | ∪ Caprimulgiformes | 43 | Hoff (1966) |
Cathartidae | ∪∨⊂ Ciconiiformes | 112 | Ligon (1967); Rea (1983); Avise et al. (1994a) |
Opisthocomidae | ∪∨⊂ Galliformes | 120 | Hudson et al. (1959); Hudson & Lanzillotti (1964) |
∪ Cuculiformes** | 22 | Avise et al. (1994b); Hughes & Baker (1999) | |
Caprimulgiformes | Polyphyly | 31 | Mayr (2002a, b) |
∪ Cypselomorphae | 42 | Mayr (2002a, 2003c, 2004d, 2005f, g) | |
Aegothelidae | ∪ Apodiformes | 31 | Mayr (2002a, 2003c, 2004d, 2005f, g) |
Steatornithidae | ∪ Trogoniformes | 102 | Mayr (2003b) |
Hemiprocnidae | ∪ Apodidae, monophyly | 5 | Sibley & Ahlquist (1990: fig. 361) |
Apodidae | ∪ Passeri (Hirundinidae) | 193 | Shufeldt (1889b); Van Tuinen (2002) |
Galbulae | ∪∨⊂ Coraciiformes | 20 | Olson (1983a) |
Coraciiformes | Δ topology, ∈ Trogoniformes | 199 | Lowe (1946); Maurer & Raikow (1981) |
Coracii | Δ topology | 64 | Cracraft (1971b) |
Menura | ∪∨⊂ Passeri | 11 | Irestedt et al. (2001); Barker et al. (2002) |
Set-symbolism coopted for concise statement of phylogenetic hypotheses, as follows: ∪, sister-group (disjoint) union; ⊂, included as subclade; ∈, included as a member taxon; ∨, or; Δ, change in; ¬, not (negation of predicate argument).
Local optima for Aepyornithiformes and Dinornithiformes (as bi-ordinal sister-group to ratites exclusive of Apterygiformes) and global optima (former as sister-group to Struthionidae and Rheidae, latter as sister-group to ratites exclusive of Apterygiformes).
Comparisons excluded effects due to differences in outgroup taxa, as well as tentatively placed Aepyornithiformes.
Doubtful comparability given differences in taxonomic samples between studies.
Corresponds to that proposed by Livezey (1998b), exclusive of Pedionomidae and fossil gruiforms (Cracraft 1969, 1971a, 1973a).
Alternative hypothesis compared sister-grouping with Cuculiformes exclusive of Musophagidae.