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NUMBER 89 181<br />

FIGURE 5.—Vulturidae, probably a new genus and species (MLP 90-X-l-l).<br />

Proximal end of radius: a, anconal view; b, palmar view. Proximal end of ulna<br />

and shaft: c, external view; d, palmar view; e, anconal view. Scale bar=l cm.<br />

lis, 61; width of midshaft, 20.8; depth of midshaft, 16.3; distal<br />

width, 46.9.<br />

REMARKS.—Before now, Geronogyps was known only from<br />

the Pleistocene sediments of the Talara Tar Seeps, Peru (Campbell,<br />

1979). Campbell established this genus based on a complete<br />

tarsometatarsus, with the distal end of a left humerus and<br />

the proximal and distal ends of two right humeri as paratypes.<br />

Because the paratypes are badly crushed, the specimens reported<br />

herein bring additional information about the morphology of<br />

Geronogyps reliquus.<br />

The following characters of Geronogyps reliquus, given by<br />

Campbell (1979), are present in the Argentinian specimen: (1)<br />

margo caudalis dropping off sharply on both sides, whereas<br />

more rounded in Vultur and Gymnogyps; (2) attachment of M.<br />

proscapulohumeralis brevis more proximal than in Vultur; (3)<br />

crista deltopectoralis flaring distally, not flaring as much in<br />

Vultur or in Gymnogyps; (4) shaft ventral to M. pectoralis superficialis<br />

not depressed, unlike Vultur and similar to Gymnogyps;<br />

(5) condylus dorsalis wide and short, whereas narrow<br />

and long in Vultur and Gymnogyps; (6) condylus ventralis<br />

short (very long in Vultur and moderately long in Gymnogyps);<br />

(7) epicondylus dorsalis long and not angular, unlike<br />

Vultur; (8) condylus ventralis gently rotated anteriad, resulting<br />

in moderately flexed distal end, as in Gymnogyps (greatly<br />

rotated in Vultur); and (9) impression of M. brachialis shallower<br />

than in Vultur or Gymnogyps.<br />

Discussion and Conclusions<br />

Condors, one of the primary scavenging lineages of birds,<br />

are large-sized vulturids with past and present distributions<br />

restricted to the New World. The fact that the temporal range<br />

of condors is less extensive in South America (middle-late<br />

Pliocene) than in North America (middle Miocene), and that<br />

their absence from the richly fossiliferous Paleogene and early<br />

Neogene outcroppings of Argentina does not seem to be<br />

related to taphonomic problems, could probably be considered<br />

a reaffirmance of Emslie's idea (1988a) about a North<br />

American origin for the group. Condors may have participated<br />

in the Great American Biotic Interchange (GABI) during<br />

Pliocene times (Webb and Marshall, 1982; Emslie, 1988a),<br />

moving from north to south across open savanna environments;<br />

however, the presence of a fossil condor, Antillovultur<br />

varonai Arredondo (1971), from the late Pleistocene of Cuba,<br />

proves that condors can cross water barriers. This fact, together<br />

with the evidence of a significant interchange of pre-<br />

Pliocene volant bird families between both Americas before<br />

the formation of a land connection (Rasmussen and Kay,<br />

1992), seems to weaken the hypothesis that condors were<br />

part of the latest events of the GABI. Our analysis does not<br />

make it possible to bring arguments in favor of, or against,<br />

this hypothesis.<br />

The fossil record summarized above indicates that a great diversity<br />

of condors occurred in the late Cenozoic of the Pampean<br />

region of Argentina, including three genera and at least<br />

four species: Dryornis pampeanus, Vultur gryphus, Gerono-

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