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© 2010 Dinosauria International Ten Sleep Report Series No. 1<br />

in part Senter’s (2007) discussion of neck elongation in<br />

sauropods, which may have been driven by sexual selection,<br />

and not by feeding competition. The height, bifurcation of<br />

neural spines, and ventral width of centra between males<br />

and females is another sexual dimorphic feature seen in the<br />

cervical vertebrae. The narrower width of the neural spines<br />

on the cervical vertebrae in DQ-SB, DQ-BS, and DQ-TY are<br />

quite slender in comparison to DQ-PE. In other words, the<br />

width of the cervical across the ribs in Prince allows it to<br />

fit over the slender female necks. Moreover, a broadened<br />

neck may also have played a role in courtship display and<br />

in male rivalry. The courtship displays may have had a<br />

cobra-like effect in their swaying heads and necks helping<br />

to appear much larger. Intraspecific combat, territorial<br />

defense, and dominance could have been achieved among<br />

males by pushing or slamming with their necks, in the<br />

same way male giraffes compete with each other using their<br />

necks and heads. The small size or absence of pleurocoel<br />

fossae in much of the vertebrae, particularly in the anterior<br />

caudals, may be a developmental male response to acquire<br />

the necessary weight needed for dominance in rivalry “push<br />

off’ battles for example. Many of the features regarded as<br />

gender specific can also be seen in young individuals. It is<br />

possible that the extreme morphological features observed<br />

in males are retained neotenic traits. For example, the long<br />

cervical ribs, short axial skeleton, and absent pleurocoels<br />

are neotenic traits that can be seen in SMA 0009 from Howe<br />

Quarry. All these features also recall the male characteristics<br />

we see in the Dana sample.<br />

Morrison diplodocids may have occupied a<br />

proboscidean-like niche with a gregarious population of<br />

males and females analogous to African elephant herds.<br />

We speculate that Apatosaurus males with larger and more<br />

massive bodies would have powerful broad necks for<br />

courtship displays and subduing females. African elephants<br />

vary greatly, but males are generally much more massive than<br />

same age adult females. In addition to overall greater size and<br />

stature, male elephants may be twice the weight of females.<br />

Principle courtship display in male elephants is their larger<br />

tusks. Amphicoelias females may have formed herds to help<br />

rear calves, which were led by a dominating harem keeping<br />

male. Males may have lived a solitary existence away from<br />

the herd appearing only during courtship. This may explain<br />

why, in the best fossil sites, Amphicoelias/Diplodocus is found<br />

in multiples while Apatosaurus, only as occasional isolated<br />

occurrences. One notable exception is in Dinosaur National<br />

Monument where three Apatosaurus specimens have been<br />

reported, but these individuals may have been washed in<br />

from further upstream.<br />

The morphological distances and occurrence<br />

between Camarasaurus and Brachiosaurus are similar in many<br />

ways to what exists in the Dana sample, thus the possible<br />

need to reconsider them as possible gender based taxa.<br />

Ontogeny<br />

Great morphological variation exists in one<br />

documented Saurischian population, the mass mortality<br />

collection of Coelophysis, from Ghost Ranch New Mexico<br />

(Colbert 1989). Colbert (1989) reports on the proportions<br />

of limb to cervical lengths, in Coelophysis, which can vary<br />

greatly, as much as 20% or more, demonstrating that axial<br />

vs. appendicular development is not equally synchronized.<br />

As exemplified in two immature specimens, DQ-TY and<br />

SMA 0009, the same ontogenetic condition appears to exist<br />

in both Amphicoelias and Coelophysis. The recognition of<br />

ontogenetic features is of great taxonomic importance not<br />

only for diplodocids but other sauropods. In addition to<br />

sexual dimorphism and individual variation, ontogeny helps<br />

to indentify character polarity in a clear biological manner.<br />

Fig 32 Comparison of illia belonging to DQ-TY and SMA<br />

0009 illustrating the elongated pubic peduncle in juveniles of<br />

Amphicoelias. Bottom row: adult Apatosaurus and Diplodocus illia for<br />

comparison. See also Fig 7C, DQ-SB. (Illustrations: Schwarz 2007,<br />

Hatcher 1903)<br />

44<br />

The baby sauropod skeleton “Toni”, described by<br />

Schwarz, et al (2007) (SMA 0009, Howe Stephens Quarry,<br />

Shell, Wyoming), belongs in the genus Amphicoelias and<br />

probably represents A. “brontodiplodocus”. Toni’s clavicle is<br />

the same boomerang-like shape as in DQ-SB and DQ-TY.<br />

Compared with the fragment described by Harris (2007)<br />

as a possible clavicle belonging to Suuwassea, the Dana<br />

Quarry clavicles are more bent and without rugosities on

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