[Date Prev][Date Next][Thread Prev][Thread Next][Date Index][Thread Index][Subject Index][Author Index]
Polar dinosaur growth and other new papers
From: Ben Creisler
bh480@scn.org
My old email has been offline for a few days so there are
a few new papers to post.
Woodward, H.N., Rich, T.H., Chinsamy, A and Vickers-Rich,
P. (2011)
Growth Dynamics of Australia's Polar Dinosaurs.
PLoS ONE 6(8): e23339.
Doi:10.1371/journal.pone.0023339
http://www.plosone.org/article/info%3Adoi%2F10.1371%
2Fjournal.pone.0023339
Analysis of bone microstructure in ornithopod and
theropod dinosaurs from Victoria, Australia, documents
ontogenetic changes, providing insight into the
dinosaurs' successful habitation of Cretaceous Antarctic
environments. Woven-fibered bone tissue in the smallest
specimens indicates rapid growth rates during early
ontogeny. Later ontogeny is marked by parallel-fibered
tissue, suggesting reduced growth rates approaching
skeletal maturity. Bone microstructure similarities
between the ornithopods and theropods, including the
presence of LAGs in each group, suggest there is no
osteohistologic evidence supporting the hypothesis that
polar theropods hibernated seasonally. Results instead
suggest high-latitude dinosaurs had growth trajectories
similar to their lower-latitude relatives and thus, rapid
early ontogenetic growth and the cyclical suspensions of
growth inherent in the theropod and ornithopod lineages
enabled them to successfully exploit polar regions.
---
David C. Evans, Paul M. Barrett, and Kevin L. Seymour
(2011)
Revised identification of a reported Iguanodon-grade
ornithopod tooth from the Scollard Formation, Alberta,
Canada.
Cretaceous Research (advance online publication)
doi:10.1016/j.cretres.2011.07.002
http://www.sciencedirect.com/science/article/pii/S01956671
11000978
Abstract
An isolated tooth from the late Maastrichtian strata of
the Scollard Formation of Alberta, Canada, has been
identified as the only record of a non-hadrosaurid
hadrosauriform from the Maastrichtian of North America.
Here, we demonstrate that this identification is in error
and that the tooth pertains to an indeterminate
ceratopsid. In addition, we provide full documentation of
the published collection of Scollard Formation fossils
from which the tooth was originally derived.
----
Schachner, E. R., Farmer, C. G., McDonald, A. T., and P.
Dodson. (2011)
Evolution of the dinosauriform respiratory apparatus: new
evidence from the postcranial axial skeleton.
The Anatomical Record (advance online publication)
DOI: 10.1002/ar.21439
http://onlinelibrary.wiley.com/doi/10.1002/ar.21439/abstra
ct
Examination of the thoracic rib and vertebral anatomy of
extant archosaurs indicates a relationship between the
postcranial axial skeleton and pulmonary anatomy. Lung
ventilation in extant crocodilians is primarily achieved
with a hepatic piston pump and costal rotation. The
tubercula and capitula of the ribs lie on the horizontal
plane, forming a smooth thoracic ??ceiling?? facilitating
movement of the viscera. Although the parietal pleura is
anchored to the dorsal thoracic wall, the dorsal visceral
pleura exhibits a greater freedom of movement. The air
sac system and lungs of birds are associated with
bicapitate ribs with a ventrally positioned capitular
articulation, generating a rigid and furrowed rib cage
that minimizes dorsoventral changes in volume in the
dorsal thorax. The thin walled bronchi are kept from
collapsing by fusion of the lung to the thorax on all
sides. Data from this study suggest a progression from a
dorsally rigid, heterogeneously partitioned,
multichambered lung in basal dinosauriform archosaurs
towards the small entirely rigid avian-style lung that
was likely present in saurischian dinosaurs, consistent
with a constant volume cavum pulmonale, thin walled
parabronchi, and distinct air sacs. There is no vertebral
evidence for a crocodilian hepatic piston pump in any of
the taxa reviewed. The evidence for both a rigid lung and
unidirectional airflow in dinosauriformes raises the
possibility that these animals had a highly efficient
lung relative to other Mesozoic vertebrates, which may
have contributed to their successful radiation during
this time period.
----
Brian M. Davis (2011)
Evolution of the Tribosphenic Molar Pattern in Early
Mammals, with Comments on the ?Dual-Origin? Hypothesis.
Journal of Mammalian Evolution (advance online
publication)
DOI: 10.1007/s10914-011-9168-8
http://www.springerlink.com/content/33n11u34336t5537/
Development of the tribosphenic molar was a fundamental
event that likely influenced the rise of modern mammals.
This multi-functional complex combined shearing and
grinding in a single chewing stroke, and provided the
base morphology for the later evolution of the myriad
dental morphologies employed by mammals today. Here a
series of morphotypes are presented that represent
stepwise acquisition of characters of the molar crown, in
an effort to clarify homologies and functional analogies
among molars of tribosphenic and tribosphenic-like
mammals, as well as their putative sister groups. This is
accomplished by evaluation of wear features, which
provide direct evidence of occlusal function, and mapping
these features on molars of the various morphotypes
demonstrates their utility in determining homology. The
original singular lower molar talonid cusp is homologous
with the hypoconid, and upper molar cusp C in early
mammals is homologous with the metacone (cusp ?C? is a
neomorph with variable occurrence). The lingual
translation of the metacone to a position more directly
distal to the paracone (as in Peramus) creates an
embrasure for the lower molar hypoconid, and is
accompanied by the development of the hypoconulid and a
new shearing surface. Lastly, the Gondwanan radiation of
tribosphenic-like mammals, the Australosphenida
(including monotremes), is determined to be functionally
non-tribosphenic. The Tribosphenida are restricted to
Laurasian taxa, with an origin at or just prior to the
Jurassic-Cretaceous boundary.