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OLOROTITAN PHYLOGENY (long)
In light of the description of the new hadrosaurid from the Amur region of
eastern Russia, _Olorotitan arharensis_, I think some necessary discussion
is due in regards to those often neglected on this list dinosaurs known as
ornithischians.
GODEFROIT ET AL. 2003's ANALYSIS
Their original analysis found the following phylogeny-
--+-- _Bactrosaurus_
`--+-- HADROSAURINAE
`-- LAMBEOSAURINAE
|-- _Tsintaosaurus
`--+-- _Jaxartosaurus_
`--+-- _Amurosaurus_
`--+-- PARASAUROLOPHINI
| |-- _Charonosaurus_
| `-- _Parasaurolophus_
`-- HYPACROSAURINI
|-- _Lambeosaurus_
`--+-- _Corythosaurus_
|-- _Hypacrosaurus_
`-- _Olorotitan_
Their outgroup, _Bactrosaurus_ was coded as "0" for all of the characters in
the analysis. However, this was incorrect for at least one character, the
ilial antitrochanter, which according to J. Head (2001), was present in
_Bactrosaurus_.
An issue of concern regarding Godefroit et al.'s analysis, is character 6
(Frontal longer than wide [0], wider than long [1]). They use a second
state for the reversal in _Parasaurolophus_, quote: secondary elongation
resulting of the backwards extension of the frontal platform [2]. It's not
necessarily the same state, but I suggest that the character be revised
perhaps to reflect only a certain part of the frontal. I've not had the
chance to see many hadrosauroid skulls (much less an ornithischian) in
dorsal view, so I when I did my analysis, I used only the first two states
and coded _P._ as having the plesiomorphy. Thoughts from others on the
list?
MY ANALYSIS OF IGUANODONTS... ERR... HADROSAUROIDS :-D
I was already working on a larger analysis of derived iguanodontians when I
decided to take a look at _Olorotitan_. I don't doubt that _Olorotitan_
wasn't a hypacrosaurinid, but I felt the need to re-run the analysis with
characters I was more sure of. My current analysis only includes characters
from Casanovas et al. 1999, Godefroit et al. 2003, and Head 2001. This
meant that if I included the more basal taxa for at least this run (such as
_Jinzhousaurus_, _Fukuisaurus_, _Probactrosaurus_, _Ouranosaurus_, and the
Horse Mane Mountain hadrosauroid) it might have made the analysis mucked up
with taxa that could not be coded as anything other than "?" or "0". I
decided to follow the phylogeny of Head 2001 and use _Eolambia_ as an
outgroup for the rest of the taxa included. I also included the Fontllonga
mandible described by Casanovas et al. 1999 and (surprise, surprise) it
occupies the same position as it did in that paper. I choose not to include
_Gilmoreosaurus_ because I lack sufficient references in order to code it
for most of Godefroit et al.'s characters. Actually, I would appreciate it
if someone could post onlist the references for the following taxa:
Tsintaosaurus, Bactrosaurus, Amurosaurus, Jaxartosaurus, Gilmoreosaurus,
Pararhabdodon, Nanyangosaurus, & Telmatosaurus.
Tree length = 56
Consistency Index = 0.8929
15 taxa, 53 characters
--+-- _Eolambia_
`--+-- _Protohadros_
|-- _Bactrosaurus_
`--+-- _Telmatosaurus_
`--+-- Fontllonga Mandible
`-- EUHADROSAURIA
|-- HADROSAURINAE
| |-- _Prosaurolophus_
| |-- _Saurolophus_
| |-- _Brachylophosaurus_
| `-- _Edmontosaurus_
`-- LAMBEOSAURINAE
|-- PARASAUROLOPHINI
| |-- _Parasaurolophus_
| `-- _Charonosaurus_
`-- HYPACROSAURINI
|-- _Olorotitan_
|-- _Corythosaurus_
|-- _Hypacrosaurus_
`-- _Lambeosaurus_
Apomorphy List (ACCTRAN)*
Fontllonga + Euhadrosauria
7(1): Dentary tooth crowns narrow
9(1): Form of dentary teeth not recurved
Euhadrosauria
6(1): Coronoid process rostrally oriented
10(1): Median carina symmetrical relative to the midline of the dentary
crown
12(1): Secondary ridges on dentary teeth absent
Hadrosaurinae
17(1): Angle between the crown and root of dentary teeth less than 130
degrees
35(1): Maxilla nearly symmetrical in lateral view
46(1): Distal end of ilium tapering distally
Lambeosaurinae
8(2): Height/mesiodistal length ratio of dentary crowns more than 3
11(1): Median carina on dentary teeth sinuous
19(1): Ratio 'length/minimal width' of the parietal less than 2
21(1): Hollow supracranial crest
23(1): Frontal wider than long
24(1): Premaxillary foramen absent
26(1): Lateral and dorsal processes of the premaxilla contact each other
behind the external naris
30(1): Caudal portion of the prefrontal participating in the lateroventral
border of the hollow supracranial crest
31(1): Lateral side of the squamosal elevated
33(1): Rostral process of the jugal truncated in lateral view
37(1): Ectopterygoid ridge strongly developed on the lateral side of the
maxilla
42(1): Deltopectoral crest of humerus strongly developed, extending down
below the mid-point of the humeral shaft
53(1): Supratemporal fenestrae rounded in dorsal view
Parasaurolophini
18(1): Parietal does not participate in the occipital region of the skull
22(1): Deeply excavated frontal platform occupying the rostral part of the
frontal in adults
47(1): Distal head of fibula greatly expanded and club-shaped
48(1): Cranial ascending process of astragalus equilateral in shape
Hypacrosaurini
25(1): Lateral premaxillary process extending further backwards past the
lacrimal
27(1): Cavum nasi proprium elongate
28(1): Nasal 50% or more of the hollow supracranial crest
*-- How do you set the character search to DELTRAN in PAUP * 4.0b10? I want
to rerun the analysis, but I don't know how to change the settings.
REFERENCES:
Casanovas, M., Pereda Suberbiola, X., Santafe, J., & Weishampel, D., 1999.
A primitive euhadrosaurian dinosaur from the uppermost Cretaceous of the
Ager syncline (southern Pyrenees, Catalonia). Geologie en Mijnbouw 78:
345-356
Godefroit, P., Bolotsky, Y., & Alifanov, V., 2003. A remarkable
hollow-crested hadrosaur from Russia: an Asian origin for lambeosaurines.
C. R. Paleovol 2: 143-151
Head, J., 2001. A reanalysis of the phylogenetic position of Eolambia
caroljonesa (Dinosauria, Iguanodontia). Journal of Vertebrate Paleontology
21(2): 392-396
nick gardner
= paleoartist
= paleogeek
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