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NUMBER 89 283<br />

These are the absence of the bicipital crest and intumescence<br />

(character 11); the absence of the pneumatic foramen in the<br />

pneumotricipital fossa, being expressed only as an undivided<br />

tricipital depression (character 12); a small ventral tubercle on<br />

the proximal end of the humems; the presence of a ligamental<br />

fossa instead of a transversal ligamental furrow (character 15);<br />

a rounded cross-section of the shaft of the radius; and the presence<br />

of an ungual phalanx on the major wing digit. These characters<br />

demonstrate that the Ambiortiformes have a common origin<br />

with other orders of paleognathous birds.<br />

Otogornis differs from Ambiortus in having a smaller procoracoid<br />

process; a deep groove on the lateral side of the shoulder<br />

end of the scapula; a wide scapular blade (narrow in Ambiortus);<br />

a flat, elongated excavation along the cranial side of the<br />

deltopectoral crest; and the presence of a capital groove, which<br />

is divided into two furrows (Figures 6, 7). Differences in the<br />

detailed morphology of the scapula and humems support their<br />

separate generic status, although it could be argued that they<br />

are only two species of a single genus.<br />

Ambiortus dementjevi is smaller than Otogornis genghisi.<br />

The maximum width of the proximal end of the humems of A.<br />

dementjevi is 13.0 mm, and the maximum width across the<br />

most projecting edge of the deltopectoral crest is 11.2 mm. The<br />

same measurements in O. genghisi are 15.8 mm and 12.2 mm,<br />

respectively.<br />

Chen, Peiji, and Zhenlu Chang<br />

1994. Nonmarine Cretaceous Stratigraphy of Eastern China. Cretaceous<br />

<strong>Res</strong>earch, 15:245-257, 4 figures.<br />

Chiappe, Luis M.<br />

1995. First 85 Millions Years of Avian Evolution. Nature. 378:349-355, 6<br />

figures.<br />

Cracraft, J.<br />

1986. The Origin and Early Diversification of Birds. Paleobiology,<br />

12:383-399, 1 table, 4 figures.<br />

Dmitriev, V.Yu., and V.V. Zherikhin<br />

1988. [The Changes of Diversity in the Insect Families on the Data by the<br />

Method of Accumulated Occurrences.] In A.G. Ponomarenko, editor,<br />

Cretaceous Biocenotic Crisis and the Evolution of Insects,<br />

pages 208-215, 1 table, 1 figure. Moscow: Nauka. [In Russian.]<br />

Dong, Zhi-Ming<br />

1993. A <strong>Lo</strong>wer Cretaceous Enantiornithine Bird from the Ordos Basin of<br />

Inner Mongolia, People's Republic of China. Canadian Journal of<br />

the Earth Sciences, 30:2177-2179, 1 table, 2 figures.<br />

Elzanowski, A.<br />

1995. Cretaceous Birds and Avian Phylogeny. Courier Forschungsinstitut<br />

Senckenberg, 181:37-53, 4 figures.<br />

Fan, Jin<br />

1996. New Advances in the Late Mesozoic Stratigraphic <strong>Res</strong>earch of<br />

Western Liaoning, China. Vertebrata Palasiatica, 34(2): 102-122, 3<br />

tables. [In Chinese, with English summary.]<br />

Literature Cited<br />

Conclusions<br />

Ambiortus from central Mongolia and Otogornis from the Ordos<br />

Basin, China, show a close relationship based on the shared,<br />

specialized characters 8, 10, and 16 in the structure of the forelimb<br />

and shoulder girdle (Table 1). At the same time, Ambiortus<br />

and Otogornis show some differences in the shoulder girdle and<br />

the forelimb that support their separate generic status.<br />

The relationships of Ambiortus and Otogornis with other<br />

birds are determined by comparison with the Ichthyomithes,<br />

Neornithes, Palaeognathae, and Neognathae. Ambiortus and<br />

Otogornis share an advanced condition of characters 7 and 9,<br />

which are common to the Ornithurae. Ambiortus shares with<br />

the Neornithes an advanced condition of characters 1 and 3,<br />

which are unknown for Otogornis. At the same time, the Ambiortiformes<br />

share with the Palaeognathae (including Lithomithiformes)<br />

such specialized characters as 5, 6, 13, and 14,<br />

which suggests their assignment to the parvclass Palaeognathae,<br />

sensu Kurochkin (1995b). No common advanced characters<br />

were found for the Ambiortiformes, Ichthyomithes, and<br />

Enantiornithes. This study confirms that the Ambiortiformes<br />

are not closely related to the Ichthyomithes or the Neognathae<br />

and are totally unrelated to the Enantiornithes.<br />

The Early Cretaceous Ambiortiformes were flying palaeognathous<br />

birds. Thereby, they document an early diversification<br />

of ornithurine birds into two main evolutionary branches:<br />

Palaeognathae and Neognathae.<br />

Feduccia, Alan<br />

1995. Explosive Evolution in Tertiary Birds and Mammals. Science,<br />

267:637-638, 2 figures.<br />

1996. Origin and Evolution of Birds, x+420 pages. New Haven and <strong>Lo</strong>ndon:<br />

Yale University Press.<br />

Harland, W.B., R.L. Armstrong, A.V. Cox, L.E. Craig, A.G. Smith, and D.G.<br />

Smith<br />

1989. A Geologic Time Scale 1989. xvi+263 pages. Cambridge: Cambridge<br />

University Press.<br />

Harrison, C.J.D., and CA. Walker<br />

1973. Wyleyia: A New Bird Humerus from the <strong>Lo</strong>wer Cretaceous of England.<br />

Palaeontology, 16:721-728, 2 figures.<br />

Hou, Lianhai<br />

1994. A Late Mesozoic Bird from Inner Mongolia. Vertebrata Palasiatica,<br />

32(4):258-266, 3 figures, 1 plate.<br />

Houde, P.<br />

1988. Paleognathous Birds from the Early Tertiary of the Northern Hemisphere.<br />

Publications of the Nuttall Ornithological Club, 22: vii+148<br />

pages, 27 tables, 41 figures.<br />

Houde, P., and S.L. Olson<br />

1981. Paleognathous Carinate Birds from the Early Tertiary of North<br />

America. Science, 214:1236-1237, 2 figures.<br />

Krassilov, V.A.<br />

1982. Early Cretaceous Flora of Mongolia. Palaeontographica, series B,<br />

Paldophytologie, 181:1-43, 1 table, 11 figures, 20 plates.

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