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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