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New Papers



Hi All -

   A few new things cropping up:

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Veevers, J.J. 2006. Updated Gondwana (Permian-Cretaceous) Earth history of Australia. Gondwana Research 9(3):231-260. doi: 10.1016/j.gr.2005.11.005.

ABSTRACT: Permo-Carboniferous glaciation, confined to icecaps and mountain glaciers, was followed by Permian coal measures and Early Triassic barren measures and redbeds, in the east terminally deformed in the mid-Triassic. Coal deposition resumed during the Late Triassic, and tholeiite was erupted in the southeast. After rifting, the western margin was formed by the opening of the Indian Ocean at 156 and 132 Ma. At 140 Ma, a brief glaciation affected central Australia. By the 99 Ma mid-Cretaceous, the southern margin was finally shaped by the opening of the southeastern Indian Ocean, the shoreline retreated to the present coast from the maximum Aptian shoreline of an epeiric sea, and the Eastern highlands were uplifted to produce the present morphology of Australia.
New data relate to the Permo-Carboniferous and Early Cretaceous glaciations, the Kiaman Reversed Paleomagnetic Interval, events about the Permian-Triassic boundary, including possible impact craters, advances in palynology, invertebrate paleontology, macrofloral paleontology, and paleobiogeography, the provenance of sediments by U-Pb ages and host-rock affinity of zircons, stable-isotopes and biomarkers in petroleum systems, coal environments, calibrating the time scale with U-Pb ages of zircons, fission-track thermotectonic imaging, geothermal energy, and terranes split off the western margin.


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Paik, I.S., and Kim, H.J. 2006. Playa lake and sheetflood deposits of the Upper Cretaceous Jindong Formation, Korea: Occurrences and palaeoenvironments. Sedimentary Geology 187(1-2):83-103. doi: 10.1016/j.sedgeo.2005.12.006.

ABSTRACT: Lake model of the Upper Cretaceous Jindong Formation in Korea was established on the basis of sedimentological and palaeobiological records of the playa lake and sheetflood deposits and their palaeoenvironmental implications. The playa lake and sheetflood deposits of the Jindong Formation are characterized by the common presence of traces of vanished evaporites, complicated polygonal desiccation cracks and rainprints, the pedogenic carbonate development, and the preservation of invertebrate traces and dinosaur and bird tracks. The traces of vanished evaporites including halite and sulphate evaporite occur as evaporite pseudopmorphs and moulds. The occurrence of all of the evaporite minerals as traces suggests that flooding stages persisted much longer than evaporation and desiccation stages. Invertebrates, birds, and dinosaurs inhabited the playa lake environment of the Upper Cretaceous Jindong Lake.
The Jindong Lake formed by the combination of humid source area and arid depositional site due to an orographic effect in fault-bounded basin. Extensive development of the playa lake and sheetflood deposits with evaporite mineral casts and very limited association of shoreline deposits in the Jindong Formation are characteristic of closed lake, and the Jindong Lake is compared to a lake formed in partly drained closed basin. The aggradation of mudflat deposits indicates continued subsidence of the basin and continuation of an underfilled lake basin. The Jindong Lake expanded and stabilized as a playa lake surrounded by dry to saline mudflats, and palaeoclimate and subsidence rates changed little throughout the period of the Jindong Lake development.




LeTourneau, P.M., and Huber, P. 2006. Early Jurassic eolian dune field, Pomperaug basin, Connecticut and related synrift deposits: stratigraphic framework and paleoclimatic context. Sedimentary Geology 187(1-2):63-81. doi: 10.1016/j.sedgeo.2005.12.005.

ABSTRACT: The discovery of an extensive eolian sandstone in the Pomperaug basin, Connecticut is noteworthy because it is the most significant occurrence of eolian rocks in the continental rifts of the Newark Supergroup south of the Fundy basin, Canada. Climate-sensitive rocks provide important constraints for the influence of supercontinent landmass configurations on models of early Mesozoic Pangaean climate. The sedimentary structures and textures in the Pomperaug basin sandstone compare favorably with modern and ancient eolian sands. The eolian sandstone is traceable for at least 5 km and occupies a stratigraphic interval that is dominated by arid facies in the Pomperaug and Hartford basins, indicating that the eolian deposit is indicative of regional climate. The eolian sands were stabilized by a return to more humid conditions and subsequently buried beneath a thick, basin-wide basalt flow, preserving the dune field. Also described are related synrift eolian sandstones from the Hartford (Connecticut, USA), Fundy (Nova Scotia, Canada), and Argana (Morocco) basins. Using revised paleolatitude models for the Pangaean rifts, the distribution of eolian sandstones suggests that the Norian-Hettangian world had zonal climate belts with modified latitudinal gradients.

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Codorniú, L., Gasparini, Z., and Paulina-Carabajal, A. 2006. A Late Jurassic pterosaur (Reptilia, Pterodactyloidea) from northwestern Patagonia, Argentina. Journal of South American Earth Sciences 20(4):383-389. doi: 10.1016/j.jsames.2005.07.014.

ABSTRACT: A small to medium-sized pterodactyloid pterosaur (wingspan approximately 1.10 m) from the Upper Jurassic (middle-late Tithonian) marine deposits of the Vaca Muerta Formation of Patagonia (Los Catutos area, central Neuquén Province, Argentina) is reported. The specimen lacks the skull but constitutes a nearly complete postcranial skeleton, which includes cervical and dorsal vertebrae; a few thoracic ribs; both pectoral girdles; the left pelvic girdle; a proximal right wing (humerus, ulna, and radius) and metacarpal IV; a left wing that lacks only wing phalanx four; and both hindlimbs, the right one without the foot. Ontogenetic features suggest that the new fossil corresponds to a relatively mature individual, probably a subadult. Observed characters support its assignment to the Archaeopteroactyloidea, a basal clade within the Pterodactyloidea. This specimen is the second pterosaur from Los Catutos and the most complete Jurassic pterosaur so far known from South America.

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Buffetaut, E., Azar, D., Nel, A., Ziadé, K., and Acra, A. 2006. First nonavian dinosaur from Lebanon: a brachiosaurid sauropod from the Lower Cretaceous of the Jezzine District. Naturwissenschaften On-line First. doi: 10.1007/s00114-006-0124-z.

ABSTRACT: Two sauropod teeth from an Early Cretaceous (Neocomian) fluviodeltaic sandstone near Jezzine (Southern Lebanon) are the first nonavian dinosaur remains to be reported from Lebanon. Their distinctive character places them within Brachiosauridae. The sauropod teeth from Lebanon are a significant addition to the very scanty dinosaur record from the Levant, which hitherto consisted mainly of very poorly preserved and not easily identifiable specimens. The Basal Cretaceous Sandstone of Lebanon, thus, appears to be a potentially important source of fossil vertebrate material.

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Buffetaut, E. 2005. Late Cretaceous vertebrates from the Saint-Chinian area (southern France): a review of previous research and an update on recent finds. Acta Palaeontologica Romaniae 5:39-48.

ABSTRACT: This paper traces the history of research on the Late Cretaceous vertebrates of the Saint-Chinian area of southern France since the first report of dinosaur bones by Gervais in 1877. A number of researchers, including Miquel, Depéret, Nopcsa and Lapparent, were involved in the early studies on this faunal assemblage, from the 1890s to the 1950s, but the known number of taxa remained low because
specimens were recovered almost exclusively by surface collecting. A faunal list showing a significantly higher diversity is presented, on the basis of recent work involving systematic excavations and screenwashing. This list includes actinopterygians, coelacanths, amphibians, turtles, squamates, crocodilians, pterosaurs, dinosaurs, birds and mammals. Fossil eggs are also common.


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Pincemaille-Quillevere, M., Buffetaut, E., and Quillevere, F. 2006. Description ostéologique de l'arrière-crâne de Rhabdodon (Dinosauria, Euornithopoda) et implications phylogénétiques. Bulletin de la Société Geologique de France 177(2):97-104.

ABSTRACT (English summary, actually): Since the 19th century, the Campanian and Maastrichtian continental deposits of southern France have yielded numerous dinosaur remains [Le Loeuff, 1991; 1998; Buffetaut et al., 1997; Laurent et al., 1991; Allain and Suberbiola, 2003]. The ornithopod remains that have not been referred to the hadrosaurids have been systematically attributed to Rhabdodon [Buffetaut and Le Loeuff, 1991; Buffetaut et al., 1996; Garcia et al., 1999; Pincemaille-Quillévéré, 2002]. This genus, initially named by Matheron [1869] after its discovery in the lower Maastrichtian of La Nerthe (Bouches-du-Rhône), belongs to the Euornithopoda [sensu Sereno, 1999]. Rhabdodon represents the most common element of the dinosaur assemblages from the late Cretaceous of southern France [e.g. Allain and Suberbiola, 2003]. Nevertheless, since the localities have only provided some fragmentary material [Pincemaille-Quillévéré, 2002], the global morphology of this dinosaur and its phylogenetic placement within the euornithopods are still debated. The cranial morphology of Rhabdodon is particularly poorly understood due to the rarity of cranial remains preserved in the localities of southern France [Matheron, 1869; Garcia et al., 1999; Buffetaut et al., 1999; Pincemaille-Quillévéré, 2002]. Buffetaut et al. [1999] first mentioned the discovery of a braincase (M4) referred to Rhabdodon, at Massecaps, a locality close to the village of Cruzy (Hérault, France). More recently, a new braincase (MN25) has been discovered at Montplô Nord, another locality close to Cruzy (specimens M4 and MN25 are conserved in the Museum of Cruzy). Both these localities have revealed a diverse and abundant vertebrate fauna suggesting a late Campanian to early Maastrichtian age [Buffetaut et al., 1999].
These braincases are described here in an attempt to detect potential autapomorphic characters in Rhabdodon, and compared to a more complete braincase of Tenontosaurus, an euornithopod from the Lower Cretaceous of North America, considered as the sister group of Rhabdodon [Weishampel et al., 1998; 2003; Garcia et al., 1999; Pincemaille-Quillévéré, 2002], in order to determine the potential differences and synapomorphies between the occiputs of the two genera. Finally, the braincases from Cruzy are compared to those of the other euornithopods described in the literature.
Specimen M4 (figs. 1-4) is incomplete but exceptionally well preserved. This braincase belongs to a juvenile individual, as shown by the numerous visible suture lines between the different cranial elements. Specimen MN25 (fig. 5) is badly deformed and attributable to an adult individual. Until now, all the ornithopods from the Upper Cretaceous of southern France have been referred either to hadrosaurs or to Rhabdodon. The Hadrosauridae show a low nuchal crest and their exoccipitals meet and form a bar on the dorsal border of the foramen magnum, excluding the supraoccipital from this border. Specimens M4 and MN25 do not present any nuchal crest and the supraoccipital participates in the dorsal border of the foramen magnum. Both braincases M4 and MN25 are therefore attributable to Rhabdodon.
Specimens M4 and MN25 have been compared to the occiput of a juvenile Tenontosaurus tilletti (fig. 6 : MCZ 4205, conserved in the Museum of Comparative Zoology, Harvard University). This reveals that Tenontosaurus and Rhabdodon share numerous characters : (1) the exoccipitals form the lateral borders of the foramen magnum, its ventral border being occupied by the basioccipital; (2) the occipital condyle is partly constituted by the exoccipitals, and in the same proportions; (3) the supraoccipital is rostrally oriented; (4) the suture line located between the prootic and the laterosphenoid shows the same outline; (5) the cresta prootica starts within the paroccipital process and extends onto the opisthotic; (6) the cresta prootica is transversal and non-horizontal; (7) the distribution of the cranial nerves is homologuous along the lateral surface of the braincase. Nevertheless, the braincase of Tenontosaurus differs from that of Rhabdodon in several significant respects : (1) the exoccipitals are dorsally connected, excluding the supraoccipital from the dorsal border of the foramen magnum; (2) two small dorsal humps are present at the level of the suture of the exoccipitals; (3) the supraoccipital is excluded from the dorsal border of the foramen magnum, which gives it a triangular shape; (4) the paroccipital processes are short, laterally flattened, and wing-shaped, and are more medio-dorsally oriented than in Rhabdodon; (5) the cresta prootica follows a concave line and ends up on the prootic, at the level of the opening of the trigeminal nerve; (6) the external curve of the laterosphenoids is stronger; (7) the suture between the basioccipital and the opisthotic is very clear. The first of these unshared characters suggests that Rhabdodon belongs to Norman's [1984] 'hypsilophodontoid' clade and Tenontosaurus to the more evolved 'iguanodontoid' clade. The fusion of the exoccipitals on the dorsal border of the foramen magnum, together with other cranial adaptations, may have reduced the stress caused by a more elaborate mastication. Rhabdodon appears to have had a more primitive type of mastication. The strip formed by the reunion of the exoccipitals is less expanded dorso-ventrally in Tenontosaurus tilletti than in the 'iguanodontoid' and 'hadrosauroid' clades. Tenontosaurus may therefore represent an intermediate group between the 'hypsilophodontoid' and 'iguanodontoid' clades.


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Ji, Q., Liu, Y.-Q., and Ji, S.-A. 2006. The Early Cretaceous Jehol Biota of northern China: feathered dinosaurs, basal birds, mammals and angiosperms, Second International Palaeontological Congress (IPC2006) Pre-Congress Excursion A5. http://www.ipc2006.ac.cn/pdf/Pre-Congress%20Excursion%20A5.pdf, 6 pp.

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Reynolds, R.E. 2006. Jurassic tracks in California; pp. 19-24 in Reynold, R.E. (ed.), Making Tracks Across the Southwest. California State University Desert Studies Consortium and LSA Associates, Inc., Zzyzx.

Hamblin, A.H. 2006. Spectrum Tracksite - also known as the Grapevine Pass Wash Tracksite; pp. 29-34 in Reynold, R.E. (ed.), Making Tracks Across the Southwest. California State University Desert Studies Consortium and LSA Associates, Inc., Zzyzx.

Milner, A.R.C., and Lockley, M.G. 2006. History, geology and paleontology: St. George Dinosaur Discovery Site at Johnson Farm, Utah; pp. 35-48 in Reynold, R.E. (ed.), Making Tracks Across the Southwest. California State University Desert Studies Consortium and LSA Associates, Inc., Zzyzx.

Difley, R., and Ekdale, A.A. 2006. Trace fossils and paleoenvironments of the Early Jurassic Kayenta Formation, Washington County, Utah; pp. 49-51 in Reynold, R.E. (ed.), Making Tracks Across the Southwest. California State University Desert Studies Consortium and LSA Associates, Inc., Zzyzx.

Lofgren, D.L., Greening, J.A., Johnson, C.F., Lewis, S.J., and Torres, M.A. 2006. Footprints on the sands of time: fossil tracks at the Raymond Alf Museum of Paleontology; pp. 52-62 in Reynold, R.E. (ed.), Making Tracks Across the Southwest. California State University Desert Studies Consortium and LSA Associates, Inc., Zzyzx.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Jerry D. Harris
Director of Paleontology
Dixie State College
Science Building
225 South 700 East
St. George, UT  84770   USA
Phone: (435) 652-7758
Fax: (435) 656-4022
E-mail: jharris@dixie.edu
and     dinogami@gmail.com
http://cactus.dixie.edu/jharris/

"Actually, it's a bacteria-run planet, but
mammals are better at public relations."
-- Dave Unwin