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Last New Papers of the Year (?)



Hi All -

   Only a little dino stuff, but at least mostly Mesozoic!

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   First, these are now "officially" out:

Buffetaut, E., G. Dyke, V. Suteethorn, and H. Tong. 2005. First record of a fossil bird from the Early Cretaceous of Thailand. Comptes Rendus Palevol 4(8):681-686. doi: 10.1016/j.crpv.2005.06.002.

ABSTRACT: We present the first known occurrence of a Mesozoic fossil bird from Thailand. The new specimen is the distal end of a left humerus, from the Early Cretaceous Sao Khua Formation in the Northeast of the country, and testifies to the presence of a medium-sized avian in these non-marine strata. This is also the first Mesozoic bird known from the whole of Southeast Asia.


Godefroit, P., H. Li, and C.-Y. Shang. 2005. A new primitive hadrosauroid dinosaur from the Early Cretaceous of Inner Mongolia (P.R. China). Comptes Rendus Palevol 4(8):697-705. doi: 10.1016/j.crpv.2005.07.004.


ABSTRACT: The right dentary of a new hadrosauroid dinosaur, Penelopognathus weishampeli, has been discovered in the Bayan Gobi Formation (Albian, Lower Cretaceous) of Inner Mongolia (P.R. China). This new taxon is characterised by its elongated, straight dental ramus, whose lateral side is pierced by about 20 irregularly distributed foramina. Its dentary teeth appear more primitive than those of Probactrosaurus, but more advanced than those of Altirhinus, both also from the Lower Cretaceous of the Gobi area. Non-hadrosaurid Hadrosauroidea were already well diversified in eastern Asia by Early Cretaceous time, suggesting an Asian origin for the hadrosauroid clade.


Mahammeda, F., É. Läng, L. Mami, L. Mekahlic, M. Benhamouc, B. Bouterfac, A. Kacemic, S.-A. Chériefa, H. Chaouatia, and P. Taquet. 2005. The 'Giant of Ksour', a Middle Jurassic sauropod dinosaur from Algeria. Comptes Rendus Palevol 4(8):707-714. doi: 10.1016/j.crpv.2005.07.001.


ABSTRACT: Continental strata of Early and Middle Jurassic age are seldom-exposed, and little is known of the history of sauropod dinosaurs prior to the neosauropod radiation of the end of the Middle Jurassic. Here, we report, in the Middle Jurassic of the Occidental Saharan Atlas (Algerian High Atlas), the discovery of a skeleton, including cranial material, of a new cetiosaurid sauropod. Chebsaurus algeriensis n. g., n. sp. represents the most complete Algerian sauropod available to date, only few remains were found before.


In the same volume is:

Apesteguía, S. 2005. A Late Campanian sphenodontid (Reptilia, Diapsida) from northern Patagonia. Comptes Rendus Palevol 4(8):663-669. doi: 10.1016/j.crpv.2005.06.003.

ABSTRACT: The fossil record of sphenodontids in the Southern Hemisphere is much longer than in Laurasia, where they became extinct after Early Cretaceous times. Recent works demonstrated the persistence of at least eilenodontine sphenodontids until the 'mid'-Cretaceous of Patagonia. Focused examination of the Los Alamitos Formation collections provided remains of Late Campanian sphenodontids. Although the phylogenetic position of these remains is still uncertain, they belong to a new, unrecorded species of sphenodontid perhaps related to opisthodontians or primitive, toothed sapheosaurs.

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   Some Mesozoic mammal papers:

Archibald, J. D., and A. O. Averianov. 2005. Mammalian faunal succession in the Cretaceous of the Kyzylkum Desert; pp. 9-22 in P. D. Polly, M. S. Springer, and Z.-X. Luo (eds.), Paleomammalogy In Honor of Professor Emeritus William Alvin Clemens, Jr. Journal of Mammalian Evolution 12. Springer.

ABSTRACT: Both metatherians and eutherians are known from the Early Cretaceous (Barremian, 125 mya; million years ago) of China, while eutherian-dominated mammalian faunas appeared in Asia at least by the earliest Late Cretaceous (Cenomanian, 95 mya). The approximately 99-93 my old (Cenomanian) Sheikhdzheili l.f. from western Uzbekistan is a small sample of only eutherians, including three zhelestids and a possible zalambdalestoid. The much better-known 90 my old (Turonian) Bissekty l.f. at Dzharakuduk in the central Uzbekistan includes 15 named and unnamed species, based on ongoing analyses. Of these, 12 are eutherians represented by at least the three groups-asioryctitheres, zalambdalestids, and zhelestids-plus an eutherian of uncertain position-Paranyctoides. Zalambdalestids and zhelestids have been argued to be related to the origin of the placental gliriforms (Euarchontoglires) and ferungulates (Laurasiatheria), respectively. Although there are four previously recognized metatherians, we believe three are referable to the deltatheroid Sulestes karakshi and the fourth, Sailestes quadrans, may belong to Paranyctoides. There is one multituberculate and one symmetrodont in the Bissekty l.f. While comparably aged (Turonian) localities in North America have somewhat similar non-therians, they have more metatherians and no eutherians. The next younger localities (early Campanian, ~80 mya) in North America have both a zhelestid and Paranyctoides, suggesting dispersal of eutherians from Asia. At Dzharakuduk, the approximately 85 my old (late Turonian/Coniacian) Aitym l.f. is much less well known than the Bissekty l.f., but yields nearly identical taxa, with two non-therians, one metatherian, and six eutherians.


Wilson, G. P. 2005. Mammalian faunal dynamics during the last 1.8 million years of the Cretaceous in Garfield County, Montana; pp. 53-76 in P. D. Polly, M. S. Springer, and Z.-X. Luo (eds.), Paleomammalogy In Honor of Professor Emeritus William Alvin Clemens, Jr. Journal of Mammalian Evolution 12. Springer.


ABSTRACT: This study provides an analysis of biotic change in successive mammalian communities during the last 1.8 million years of the Cretaceous (67.3-65.58 Ma) from the Hell Creek Formation in Garfield County, Montana. Results show changes in relative abundances of species, mean individual body size, and to some extent taxonomic composition through the Hell Creek Formation. These results are interpreted as "normal" mammalian responses to fluctuating temperatures during the latest Cretaceous. By contrast, the extinction of 22-27 mammalian species at or near the Cretaceous-Tertiary (K-T) boundary cannot be explained by the coincident cooling interval alone. At the scale of temporal resolution available, these fossil data are inconsistent with an extended gradual pattern of extinction (linear-response) and are most consistent with either a non-linear response pattern for the K-T extinction, resulting from the accumulated stress of multiple long- and short-term environmental perturbations (e.g., climate change, sea-level regression, volcanism, an extraterrestrial impact), or a single, short-term cause (an extraterrestrial impact).


...and not quite Mesozoic:

Gunnell, G. F., and N. B. Simmons. 2005. Fossil evidence and the origin of bats; pp. 209-246 in P. D. Polly, M. S. Springer, and Z.-X. Luo (eds.), Paleomammalogy In Honor of Professor Emeritus William Alvin Clemens, Jr. Journal of Mammalian Evolution 12. Springer.

ABSTRACT: The phylogenetic and geographic origins of bats (Chiroptera) remain unknown. The earliest confirmed records of bats date from the early Eocene (approximately 51 Ma) in North America with other early Eocene bat taxa also being represented from Europe, Africa, and Australia. Where known, skeletons of these early taxa indicate that many of the anatomical specializations characteristic of bats had already been achieved by the early Eocene, including forelimb and manus elongation in conjunction with structural changes in the pectoral skeleton, hind limb reorientation, and the presence of rudimentary echolocating abilities. By the middle Eocene, the diversification of bats was well underway with many modern families being represented among fossil forms. A new phylogenetic analysis indicates that several early fossil bats are consecutive sister taxa to the extant crown group (including megabats), and suggests a single origin for the order, at least by the late Paleocene. Although morphological studies have long placed bats in the Grandorder Archonta, (along with primates dermopterans, and tree shrews), recent molecular studies have refuted this hypothesis, instead strongly supporting placement of bats in Laurasiatheria. Primitively, proto-bats were likely insectivorous, under-branch hangers and elementary gliders that exploited terminal branch habitats. Recent work has indicated that a number of other mammalian groups began to exploit similar arboreal, terminal branch habitats in the Paleocene, including multituberculates, eulipotyphlans, dermopterans, and plesiadapiforms. This may offer an ecological explanation for morphological convergences that led to the erroneous inclusion of bats within Archonta: ancestral archontan groups as well as proto-bats apparently were exploiting similar arboreal habitats, which may have led to concurrent development of homoplasic morphological attributes.

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Schnyder, J., A. Ruffell, J.-F. Deconinck, and F. Baudin. 2006. Conjunctive use of spectral gamma-ray logs and clay mineralogy in defining Late Jurassic-Early Cretaceous palaeoclimate change (Dorset, U.K.). Palaeogeography Palaeoclimatology Palaeoecology 229(4):303-320. doi: 10.1016/j.palaeo.2005.06.027.

ABSTRACT: Detrital clay mineralogy is controlled by weathered source rock, climate, transport and deposition that in turn influence the spectral gamma-ray (SGR) response of resultant sediments. Whilst a palaeoclimate signal in clay mineralogy has been established in some ancient successions, the SGR response remains contentious, largely because the data sets have yet to be collected at the same or appropriate vertical scales to allow comparison. In addition, the influence of organic matter on SGR is not always considered. Here, we present clay mineralogical, total organic carbon (TOC) and SGR analyses from the late Jurassic and early Cretaceous of the Wessex Basin, a period of previously documented palaeoclimate change. The aim of this paper is to estimate the sensitivity of SGR as palaeoclimatic tool, SGR and clay mineral data having been collected at the same sample points, making this one of the most rigorous comparison of clay mineral and SGR to date. Overall, the correlation between high thorium/potassium or thorium/uranium and kaolinite associated with a well-established palaeoclimate change shows that elevated thorium may be used as a proxy for humid palaeoweathering, as suggested by few previous studies.

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Fielding, S., D. M. Martill, and D. Naish. 2005. Solnhofen-style soft-tissue preservation in a new species of turtle from the Crato Formation (Early Cretaceous, Aptian) of north-east Brazil. Palaeontology 48(6):1301-1310. doi: 10.1111/j.1475-4983.2005.00508.x.

ABSTRACT: The partial, articulated skeleton of a pleurodiran turtle from the Nova Olinda Member of the Crato Formation (Araripe Basin) of north-east Brazil displays an impression of the outline of the soft tissues surrounding the left hind limb. The external mould of the soft tissue surface preserves only the gross morphology of the limb although the outline of the limb is well defined. It appears to be an external mould of the limb's surface, which formed prior to the decay of the integument. The limb skeleton is mostly fully articulated. This style of preservation is comparable with the mouldic preservation found in such famous fossils as the feathered Archaeopteryx specimens of the Solnhofen limestone. Although soft-tissue preservation is occasionally encountered in the Crato Formation, this is the first documented occurrence of mouldic preservation of body outline reported for this Konservat-Lagerstätten. The new specimen is referred to the pelomedusoid Araripemys and represents a new species, A. arturi sp. nov., which is described here.

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Fang, X., Z. Zhang, X. Zhang, L. Lu, Y. Han, and P. Li. 2005. Fossil eggs from the Heyuan Basin, east-central Guangdong, China. Geological Bulletin of China 24(7):682-686.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
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/
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