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278<br />

ment of the radius that are continued from the main slab (Figures<br />

2, 3). This slab also bears several impressions of the wing<br />

feathers. The counterslab and associated slab form a broken<br />

contact with each other (Figure 3).<br />

VERTEBRAE.—The preserved 15 or 16 cervical and thoracic<br />

vertebrae (3-17(18)) are ventrally exposed on the main slab<br />

(Figures 1, 3, 5). The first (atlas) and second (axis) vertebrae<br />

are absent, although a probable fragment of the latter is preserved<br />

in front of the first preserved vertebra, which I consider<br />

to be the third cervical. The first two preserved vertebrae each<br />

have a short, wide, flat ventral body surface; thus, I consider<br />

them to be the third and fourth cervicals. Most of the portions<br />

of the probable fifth and sixth cervicals are disarticulated from<br />

the other vertebrae. The seventh and eighth vertebrae each<br />

show a long, flattened body ventrally. They have well-developed<br />

cranial zygapophyses with costal processes and caudal<br />

zygapophyses (Figures 1, 3, 5). The carotid processes form a<br />

shallow open carotid canal. The strong, paired, caudal, transverse<br />

processes are developed on the ventral side lateral to the<br />

caudal articular surface. Such processes are present in Lithornis<br />

and in Rhea; they are different from the postlateral processes in<br />

grebes (Zusi and Storer, 1969).<br />

The ninth cervical was extracted in order to investigate the<br />

articular surfaces of the vertebral bodies because in earlier papers<br />

the vertebrae of Ambiortus were regarded as probably<br />

amphicoelous. Although this was widely used to establish the<br />

relationships of this bird, it appears to have been a misinterpretation.<br />

As a result of this new preparation of the vertebrae,<br />

it has become evident that the caudal articular surface of the<br />

eighth cervical and the cranial surface of the tenth cervical<br />

were certainly heterocoelous. The tenth and eleventh vertebrae<br />

have a longer centrum with a narrower ventral side than do<br />

those of the third and fourth vertebrae and those of the thirteenth<br />

through sixteenth vertebrae, but they have shorter centra<br />

than in the seventh and eighth vertebrae. The twelfth, thirteenth,<br />

and fourteenth cervical vertebrae show shortened<br />

bodies and enlarged costal processes represented only by the<br />

sturdy basal portions. The basal portions of two well-expressed<br />

ribs are preserved near the right side of the fifteenth<br />

vertebra. These ribs are small and represent the floating ribs.<br />

The sixteenth vertebra is very compressed. The seventeenth<br />

vertebra has a wide and nearly flat ventral body surface and a<br />

very narrow caudal articular surface. On the left side of this<br />

vertebra the dorsal portion of a large rib is present; it has two<br />

articular facets, although the dorsal one is not preserved in this<br />

sample. A probable portion of the eighteenth vertebra is preserved<br />

caudal to the seventeenth vertebra in the angle between<br />

the coracoid and sternum. The thirteenth through seventeenth<br />

vertebrae have shortened bodies. The ventral crests (hypapophyses)<br />

are not present in either the cranial cervical or the thoracic<br />

vertebrae. I think that this specimen preserves at least 15<br />

cervical vertebrae, which mainly have wide and short centra.<br />

Thus, Ambiortus was a short-necked bird.<br />

SMITHSONIAN CONTRIBUTIONS TO PALEOBIOLOGY<br />

FIGURE 2.—Associated slab with Ambiortus dementjevi, PIN 3790-272; Khurilt<br />

Ulan Bulak locality, central Mongolia, Neocomian. (Scale bar= 1 cm.)<br />

SHOULDER GIRDLE.—The cranial portion and left costal<br />

margin of the sternum preserves the base of a thick pillar of the<br />

sternal keel and a damaged sternal costal margin (Figures 1, 3).<br />

The cranial surface of the pillar is directed down and somewhat<br />

caudally. The furcula is represented by the dorsal portions of<br />

both clavicles, which terminate at slightly thinned ends that are<br />

neither enlarged nor flattened. The small articular facet for the<br />

coracoid is directed caudomedially. The cross section of the<br />

clavicle in its middle portion is nearly circular. The medial side<br />

of the clavicle is slightly flattened. Originally, the holotype<br />

preserved the mold of the interclavicular symphysis, which was<br />

placed superficially on the level of the fifteenth vertebra. This<br />

was destroyed during preparation. The mold of the ventral furcula<br />

showed that the ventral portion of both clavicles have the<br />

same diameter as dorsal ones. In the interclavicular area, a thin,<br />

slightly projecting eminence around the symphysis was<br />

present, without any vestige of the hypocleideum.<br />

In the left scapula, the caudal end of the scapular body is absent.<br />

The humeral articular facet is flat and wide and faces latero-cranially<br />

but is not nearly perpendicular to the scapular<br />

blade as noted by Elzanowski (1995). In its cranial area, the<br />

facet converges into a slightly convex, ellipsoidal coracoidal<br />

tubercle. A strongly projecting and sturdy acromion is very distinctive<br />

for this scapula (Figure 4). The acromion is dorsoventrally<br />

compressed, and its cranial ending is blunt and attenuated<br />

cranially. The dorsal surface of the acromion possesses a conspicuous<br />

dorsal tubercle (not crest) that is very similar to that in<br />

Lithornis celetius Houde, 1988. The acromion is not turned<br />

mediad, contrary to Elzanowski (1995). The scapular body is<br />

blade-like, strongly flattened lateromedially, and slightly

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