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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-