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Here are some new ones...

JT Paleobiology.                                   
DA Fall 1996 v 22 n 4
PG 496
AU Bennett, S. Christopher
TI Aerodynamics and thermoregulatory function of the dorsal sail of
   Edaphosaurus

JT Journal of the geological society
DA NOV 01 1996 v 153 p 6
PG 873   
AU Cruickshank, A.R.I.   
AU Martill, D.M.   
AU Noe, L.F.   
TI A pliosaur (Reptilia, Sauropterygia) exhibiting pachyostosis from the
Middle Jurassic of England

JT Geology.
DA NOV 01 1996 v 24 n 11
PG  963-7
AU Schultz, Peter H.   
AU D'Hondt, Steven   
TI Cretaceous-Tertiary (Chicxulub) impact angle and its consequences
AB The Chicxulub impact structure exhibits asymmetries in its geophysical
signatures that closely resemble asymmetries produced by oblique impacts in
laboratory experiments and recognized on planetary surfaces, These
asymmetric signatures suggest a trajectory for the Chicxulub bolide from
the southeast to the northwest at a 20 degrees-30 degrees angle from the
horizontal.  As a result, biotic extinctions may have been most severe and
catastrophic in the Northern Hemisphere, Geographic variation in the
magnitude of the Cretaceous-Tertiary (K-T) ''fern spike'' and palynofloral
extinctions are consistent with the proposed trajectory.

M. Szpir 1997, Science Observer: Perturbing the Oort cloud, American
Scientist, 85(1):23

L.J. Penvenne 1997, The bolide and the biosphere, American Scientist,
85(1):25

JT Palaeontology.
DA DEC 01 1996 v 39 p 4
PG 883   
AU Gower, D.J.   
AU Sennikov, A.G.   
TI Morphology and phylogenetic informativeness or early archosaur
braincases

JT Scientific American.
DA FEB 01 1997 v 276 n 2
PG 16   
TI Science and the Citizen.
SU Birds and dinosaurs

JT Insight on the news.
DA JAN 20 1997 v 13 n 2
PG 31   
AU Goode, Stephen   
TI Books.
SU Dinosaurs are forever.

JT Cretaceous research.
DA DEC 01 1996 v 17 n 6
PG  741     
AU Kozaric, Z.   
AU Parica, M.   
AU Bajraktarevic, Z.   
TI Histological bone structure of Lower Cretaceous dinosaurs from southwest
Istria (Croatia).

JT Current science.
DA JUN 10 1996 v 70 n 11
PG  990     
AU Venkatesan, T. R.   
AU Pande, Kanchan   
AU Ghevariya, Z. G.   
TI 40Ar-39Ar ages of Anjar Traps, Western Deccan Province(India) and its
relation to the Cretaceous-Tertiary Boundary events

JT Canadian journal of earth sciences
DA DEC 01 1996 v 33 n 12
PG 1655-67 
AU Zelenitsky, Darla K.   
AU Hills, L.V.   
AU Currie, Philip J.   
TI Parataxonomic classification of ornithoid eggshell fragments from the
Oldman Formation (Judith River Group; Upper Cretaceous), southern Alberta

JT Current science.
DA MAR 10 1996 v 70 n 5
PG  399     
AU Salil, M. S.   
AU Shrivastava, J. P.   
TI Trace and REE signatures in the Maastrichtian Lameta Beds for the
initiation of Deccan volcanism before KTB

JT Geophysical journal international.
DA DEC 01 1996 v 127 n 3
PG  F11     
AU Connors, M.   
AU Hildebrand, A.R.   
AU Halpenny, J.F.   
TI Yucatan karst features and the size of the Chicxulub crater

JT Science.                                        
DA NOV 29 1996 v 274 n 5292
PG 1549   
AU Martin, R.E.
AU Vermeij, G.J.
AU Grotzinger, J.P.
TI Late Permian Extinctions.
SU Response: P.B. Wignall, R.J. Twitchett

JT Geoscientist.
DA NOV 01 1996 v 6 n 6
PG   27     
AU Trueman, C.   
TI Variation of REE patterns in dinosaur bones from North West Montana:
 implications for taphonomy and preservation

JT Proceedings of the National Academy of Sciences 
DA DEC 10 1996 v 93 n 25
PG 14623
AU Erickson, G.M.
TI Incremental lines of von Ebner in dinosaurs and the assessment of tooth
replacement rates using growth line counts

JT Palaeogeography, palaeoclimatology, palaeoecolog
DA NOV 01 1996 v 126 n 1 / 2
PG 161-71
AU Kolodny, Y.   
AU Luz, B.   
AU Sanders, M.
AU Clemens, W.A.   
TI Dinosaur bones: fossils or pseudomorphs? The pitfalls of physiology
 reconstruction from apatitic fossils
AB A prerequisite to any attempt to reconstruct thermophysiology of ancient
animals through analysis of stable isotopes of oxygen is the assumption
that apatitic fossils are isotopically unaltered parts of their original
skeletons.  We suggest that sufficient evidence is available to seriously
question this assumption.  Because living bones contain about 1/3 by weight
of organic matrix, mass balance considerations show that at least half of
an apatitic fossil must be new material added post mortem. Furthermore,
living apatitic skeletons contain almost no rare earth elements and
uranium, whereas apatitic fossils bear high concentrations of these
elements.  Additionally we found that while in living fish correlation
between delta(18)O of oxygen in the phosphate and that in the carbonate of
apatite is poor, these two values are linearly correlated in fossil fish. 
This suggests diagenetic recrystallization has taken place.  Perfect
preservation of micro-textures such as Haversian canals does not prove the
pristine condition of a fossil; some of the most beautifully preserved
fossils are highly silicified.  Most apatitic fossils probably are
pseudomorphs replacing original skeletal elements.  Whereas distribution of
stable isotopes of oxygen in fossils might provide information about their
burial environment, it could be misleading in attempts to interpret the
organisms' physiology. This cautionary note is supported by the similarity
of delta(18)O(p) in bones of coexisting fossil fish, dinosaurs, and various
other reptiles at different latitudes.  The overlap of predicted
delta(18)O(p) values in fish and mammals living in contact with the same
environmental water also weakens the hope that ectotherms can be
distinguished from endotherms by the isotopic composition of oxygen in
their bones and teeth.

JT Discover.                                       
DA FEB 01 1997 v 18 n 2
PG 26
TI Geology Watch.
SU The burning of the North American dinos

-Mikiel

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