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THE KOREAN JOURNAL OF QUATERNARY RESEARCH Vol. 21, No. 2, p. 49-53 (December. 2007)

Mongolian Hadrosaurids: Paleobiogeography, Dispersal and Environmental Relationships

Khishigjav Tsogtbaatar, Chinzorig Ts. Paleontological Center, Mongolian Academy of Sciences, Ulaanbaatar‐210351, Enkhtaivan street‐63

1. Introduction angustirostris Rozhdestvensky, 1952 (Hadrosaurinae) and Barsboldia sicinskii Maryanska et Osmolska, 1981 Hadrosaurids were the most diverse large vertebrate () during the Late , and are most However only two species have been described from thoroughly studied in terms of phylogenetics , several indeterminable hadrosaurids were re- (e.g., Taquet,1976; Sereno,1986; Horner,1990; ported from different sites in Mongolia as follows: Bayn Weishampel et al., 1993) functional morphology (e.g., Bologay (Gilmore,1933), Bayn Shireh (Maleev 1956), Ostrom, 1961; Norman, 1984; Weishampel, 1984), bio- Bugeen Tav (Trofimov et al. 1970), Shereegeen Gashoon geography (e.g., Brett‐Surman, 1979; Milner and Norman, (Rozhdestvensky 1974), Bayn Dzak and Khermeen Tsav 1984), and paleoecology (e.g., Norman and Weisampel, (Gradzinski et al.1977), Baishin Tsav (Tsybin and 1985; Weisampel and Norman, 1989) in United States Kurzanov 1979). and Europe. With few exceptions, they are considered During the field work Japan ‐ Mongolian Joint to be the natural crown group of a gradation of iguano- Paleontological Expedition since 1993 several articulated dontian taxa, and are commonly thought to have origi- and associated specimens of Hadrosaurid have nated in eastern with subsequent migrations during been found from the Bayn Shire Formation at the localities the into and Europe Baishin Tsav, Khuurai Tsav, Khongil Tsav, Bayn Shire (Weshampel and Horner, 1990). in Eastern Gobi region, Djadokhta Formation at the local- Hadrosauridae is composed of two derived, multiple‐ ities Alag Teg, Tugrikin Shire in the Central Gobi region taxon sister lineages and several primitive taxa. The de- and the at the localities Bugin Tsav, rived lineages are the large, wide‐beaked Hadrosaurinae, Gurilin Tsav and Nemegt in Western Gobi region. and the smaller, often crested Lambeosaurinae. According to the newly discovered those materials Hadrosaurids were less abundant and diverse ver- from Gobi regions expand to contribute knowledge of tebrates in Asia compared to North America during the spato‐temporal distribution of Mongolian hadrosaurs. the Late Cretaceous but have been studied by Riabinin (1925,1930,1939), Wiman(1929), Gilmore(1933), Young(1958), Rodzhestvensky(1968) and Maryanska 2. Data and Model Description and Osmolska(1981,1984). Although more than 20 hadrosaurid taxa have been # Bayn Shirenian Hadrosauroids (Santon‐Senomanian described from Asia ( five of which should be considered ‐ 99‐86 mya) as nomina dubia) only two species have thus far been described from the territory of Mongolia: One of the most important finding among collected

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specimens is almost complete skeletons of hadrosauroid the present cladistic analysis shows that with best preservation were found at first from Baishin is by far more primitive than any known typical Tsav in 1995 then from Khuurai Tsav in 2004 (Bayn Hadrosauridae. The correla- Shire Formation, Late Cretaceous). tion between the and the Bayn The fossils in Baishin Tsav is preserved in a mean- Shire Formation is based on similarities in lithofacies dering fluvial system. The key to this interpretation and fossil vertebrate assemblages worked out by Currie are large scale inclined heterolithic strata, between & Eberth(1993). the stratotype of the Bayn Shire which are sandwiched medium‐ and small‐scale trough Formation with typical vertebrate fauna of the Baynshire cross stratification. The fluviial system apparently had age that comprises of the lower part of the Upper a low energy floodplain, which is exposed as a laminated Cretaceous stratigraphic sequence. The sediments at Bayn mudstone at the base of the fossil‐bearing unit Shire were probably deposited near the end of C34n, (Fastovsky,1996). based on the preliminary paleomagnetic results that Hadrosaurid specimens have been found before from Baynshurenian time extended into a ‐ Baishin Tsav by Soviet Mongolian Joint Paleontological Santonian age (Hicks et al., 1999) Expedition and it was identified as Arstanosaurus sp. (Hadrosaurinae) by Kurzanov S.M. Arstanosaurus was # Djadokhtian Hadrosaurids (Campanian‐Santonian‐ erected by Shilin and Suslov in 1982 based on a frag- 86‐71 mya) mentary maxilla and distal fragment of femur collected from Aral region in ex‐USSR. In 1995, the joint expedition team excavated more Detailed morphological study on the newly dis- than 20 juvenile individuals of ankylosaur Pinacosaurus covered specimens from Baishin Tsav revealed that they from Alag Teg locality with Djadokhtian age. Those did not belong to “Arstanosaurus”, but were assigned specimens were discovered in mudstone (siltstone) in to the Lambeosaurinae, Bactrosaurus that was found in the position of up side down and normal. Besides the Iren Dabasu, , . Cranial and pelvic specimens of Pinacosaurus, two partial skeleton of ha- characters of the examined specimen suggest their close drosaurus were discovered. One skeleton preserved a relationship to the Lambeosaurine hadrosaurids. As taxon part of skull. Another one supplied well‐preserved hind “Arstanosaurus” is based on poorly preserved specimen limb bones and vertebrae. The third specimens of the without definite taxonomic character, it should be consid- hadrosaurus showed interesting preservation condition, ered as invalid taxon. namely, nearly vertically situated articulated metatarsals Specimens of Hadrosauroid were found from the and digits in the mudstone that was the same one yielded Baynshire Formation of Upper Cretacelous localities as the second skeleton. The hadrosaurian skeletons in this follows: Baishin Tsav, Khongil Tsav, Bayn Shire, Amtgai locality showed interesting taphonomic preservation and Khuurai Tsav. situation. Hadrosauriod specimen from Bayn Shire Formation Sedimentary environment of Alag Teg is braided was determined as Bactrosaurus, the most primitive river system (fluvial) (D. E. Fastovsky). The fluvial se- of lambeosaurine , holotype of this genus was found quence is overlain by eolian sandstone that is observed from the Iren Dabasu Formation in PRC. A Cenomanian typically in Tugurikin Shire. This stratigraphic relation- age was suggested for this formation by Rozhdestvensky ship indicates the braided river environments were re- (1966, 1974,1977). Currie & Eberth (1993) have been placed by the eolian environments. The difference of able to propose, at an extreme end of their range, a the environments affected the faunal compositions of Campanian age for the Iren Dabasu deposits. Indeed, dinosaur in both sediments (fluvial and eolian).

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The partial skull of Hadrosaurid dinosaur which were etons derived from the Altan Ula, Tsagaan Khushuu found from mudstone layer at Alag‐Teg has number of and Nemegt localities. During the Polish‐Mongolian primitive characteristics, including elongated facial re- Paleontological Expeditions several other specimens of gion, mandibular condyle of quadrate is transversely ex- this species were collected from the Nemegt Formation. panded, short and shallow braincase, denticulated oral One complete skeleton of a young individual was found margin of predentary all of which are more common at the locality Altan Ula IV. The skull of this specimen to the basal hadrosaurids than advanced hadrosaur‐sau- provided some new data on the circumorbital and crestal rolophus angustirostris from the Nemegt Formation in regions (Maryanska and Osmolska 1979). Western Gobi Desert. This is probably new genera and Almost complete very large skeleton without skull species of Hadrosaurid dinosaur from Djadokhta and/or of Saurolophus was found from the Nemegt Formation Barun Goyot Formation. The correlation of fossil verte- in Gurilin Tsav locality by Mongolian paleontologists brate assemblages from Djadokhta and Barun Goyot in 1987. Then complete skeleton with skull was found Formations has been reviewed by Lillegraven & from Bugin Tsav locality by JMJPE in 1995 McKenna(1986). These authors suggest that the assemb- Specimens of Saurolophus angustirostris were dis- lages are temporal equivalents of the younger and older covered from the Nemegtian Formation of those localities parts of the Judithian of middle Campanian. The speci- as Nemegt, Altan Ula II & IV, Tsagan Khushu, Bugin mens are belonging to the new species were found from Tsav and Gurilin Tsav in Western Gobi Desert of the localities Alag Teg and Tugrikin Shire and adjacent Mongolia. region. Another advanced hadrosaurid which was discovered from Mongolia is Barsboldia sicinskii Maryanska and Nemegtian Hadrosaurids (Maastrichtian‐71‐65 mya) Osmolska, 1981. Incomplete postcranial skeleton of Barsboldia sicinskii was found in the Late Cretaceous Hadrosaurid dinosaurs of Nemegt formation in sandy deposits of the Nemegt formation, at the Nemegt Mongolia is characterized by Saurolophus angustirostris locality (Northern Sayr) in 1970. It displays a ridged Rozhdestvensky, 1952 and Barsboldia sicinskii sacrum and comparatively long neural spines, both char- Maryanska and Osmolska, 1981. Mongolian Saurolophus acters diagnostic of the Lambeosaurinae. angustirostris and North American Saurolophus osborni The similarity of dinosaur’s assemblages including have a close relationship. Hadrosaurids between the North America and East Saurolophus angustirostris, may be the strati- Asia is occured the end of Late Cretaceous graphically youngest Asian duck‐billed dinosaur, prob- (Maastrichtian). Twelve of the dinosaur families were ably not older than the late Campanian. Representatives discovered at both ; , of the hadrosaurian genus Saurolophus occur both in Dromaeosauridae, , Oviraptoridae, Mongolia and western Canada. The North American spe- , Diplodokidae, Camarasauridae, cies has been collected in strata of early Maastrichtian Hadrosauridae, Pachycephalosauridae, Neoceratopsia age. and Ankylosauridae. Only was en- Saurolophus angustirostris was preliminary de- demic to Asia. And two families ( and scribed by Rozhdestvensky (1952) who later added (1965) Nodosauridae) are not known to occur in Mongolia. some comments on its allometric changes.The original The distribution patterns of these families suggest material of S. angustirostris collected by the Mongolian that their pre‐Kimmeridgian dichotomy was a vicariance Paleontological Expedition of the USSR ‐Academy of event generated by geographical isolation. From the Sciences in 1947‐1949 includes several complete skel- Bajocian to the Maastrichtian, East Asia is mostly isolated

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from the other continents by the Obik (Turgai) shelf‐sea Perspectives. Cambridge University Press, to the west and the Bering Seaway to the east. An early Cambridge. Pp. 179–187. Cretaceous regression could have permitted terrestrial Lillegraven, J. A., and McKenna, M. C. 1986. Fossil faunal exchange across the Obik region, while late mammals from the “Mesaverde” Formation (Late Cretaceous continental movements produced the Cretaceous, Judithian) of the Bighorn and Wind Beringian corridor from the Campanian onwards. River Basins, Wyoming, with definitions of Late Cretaceous land‐mammal “ages.” Am. Mus. Novit. 2840: 1–68. References Maryanska T.,Osmolska H., 1979 Aspects of Hadrosaurian Cranial anatomy Lethaia Vol.12, Brett‐Surman M.K. (1979) Phylogeny and pp.265‐273. Oslo Palaeobiogeography of Hadrosaurian Maryanska T.,Osmolska H., 1981 First Lambeosaurine dinosaurs.Nature Vol.277, pp.560‐562 dinosaur from the Nemegt Formation, Upper Currie, P. J., and Eberth, D. A. 1993. Palaeontology, Cretaceous, Mongolia. Acta Palaeontologica sedimentology and palaeoecology of the Iren Polonica, Vol.26, No.3/4, pp.243‐255 Dabasu Formation (Upper Cretaceous), Inner Maryanska T.,Osmolska H., 1981 Cranial anatomy of Mongolia, People’s Republic of China. Cret. Res. Saurolophus angustirostris with comments on the 14: 127–144. Asian Hadrosauridae (Dinosauria) Acta Fastovsky, D. E., Badamgarav, D., Ishimoto, H., Watabe, Palaeontologia Polonica No.42,pp.5‐24 Results of M., and Weishampel,D. B. 1997. The paleoenviron- PMPE‐Part IX ments of Tugrikin‐Shireh (Gobi Desert, Mongolia) Maryanska T.,Osmolska H., 1984 Postcranial anatomy and aspects of the taphonomy and paleoecology of Saurolophus angustrostris with comments on of (Dinosauria: ). other Hadrosaurs.Palaeontologia Polonica, 46, 119‐ Palaios 12: 59–70. 141 Gilmore C.W. (1933). On the dinosaur fauna of the Iren Milner A.R., Norman D.B. (1984) The biogeography Dabasu Formation. Bull. Am. Mus. Nat. Hist. 67: of advanced ornithopod dinosaurs (Archosauria: 23‐78 Ornithischia)‐a cladistic‐vicariance model. Third Gradzínski, R., Kielan‐Jaworowska, Z., and Maryanska, Symposium on Mesozoic Terrestrial Ecosystems, T. (1977). Upper Cretaceous Djadokhta, Baron Short Papers. 145‐150 Goyot and Nemegt Formations of Mongolia, includ- Norman D.B. (1984) A systematic reappraisal of the ing remarks on previous subdivisions. Acta Geol. reptile order Ornithischia. In: Reif, W.‐E., and Polonica 27: 281–318. Westphal, F. (eds.). Third Symposium on Mesozoic Hicks, J. F., Brinkman, D. L., Nichols, D. J., and Watabe Terrestrial Ecosystems, Short Papers. Attempto M. (1999). Paleomagnetic and palynologic analyses Verlag, Tübingen. Pp. 157–162. of Albian to Santonian strata at Bayn Shireh, Norman, D. B., and Weishampel, D. B. 1985. Ornithopod Burkhant, and Khuren Dukh, eastern Gobi Desert, feeding mechanisms: Their bearing on the evolution Mongolia. Cret. Res. 20: 829–850. of herbivory. Am. Nat. 126: 151–164. Horner J.P. (1990) Evidence of diphyletic origination Ostrom J.H. (1961) Cranial Morphology of the of the hadrosaurian (Reptilia: Ornithischia) Hadrosaurian Dinosaurs of North America Bulletin dinosaurs. In: Carpenter, K., and Currie, P. J. (eds.). American Museum of Natural History Dinosaur Systematics: Approaches and Vol.122,Article 2. pp.33‐186

- 52 - Khishigjav Tsogtbaatar, Chinzorig Ts.

Riabinin A.N. (1930) [Mandschurosaurus amurensis nov. Tsybin Y.I and Kurzanov S.M. (1979) [New data on gen., nov. sp., a hadrosaurian dinosaur from the Upper Cretaceous localities of vertebrates of Upper Cretaceous of the Amur River]. Soc. Baishin Tsav region] Trudy Sovmestnoi Sovetsko‐ Paleontol. Russ. Mem. 2: 1–36. (In Russian.) Mongol’skoi Paleontologicheskoi Ekspeditsii 8: 08 Rozhdestvensky, A. K. 1952a. [A new representative ‐111 of the duck‐billed dinosaurs from the Upper Weishampel D.B. (1984) Evolution of Jaw Mechanisms Cretaceous deposits of Mongolia]. Dokl. Akad. in Ornithopod Dinosaurs Springer‐ Nauk S.S.S.R. 86: 405–408. (In Russian.) Verlag,Berlin,Heidelberg, New York, Tokyo Rozhdestvensky, A. K. 1968b. [Hadrosaurs of Weishampel, D. B., and Norman, D. B. 1989. Vertebrate Kazakhstan]. In: Tatarinov, L. P. (ed.). [Upper herbivory in the Mesozoic: Jaws, , and evolu- Paleozoic and Mesozoic Amphibians and Reptiles]. tionary metrics. In: Farlow, J. O. (ed.). Paleobiology Akademia Nauk S.S.S.R., Moscow. Pp. 97–141. of the Dinosaurs. Geol. Soc. Am. Spec. Pap. 238: (In Russian.) 87–100. Rozhdestvensky A.K. 1966. [New Iguanodonts from Weishampel D.B.,Norman D.B, Grigorescu D., Central Asia. Phylogenetic and taxonomic inter- (1993) transsylvanicus from the relationships of late and early Late Cretaceous of Romania: The most basal Hadrosauridae] Paleontol.Zh. 1966: 103‐116 (In Hadrosaurid dinosaur. Palaeontology, Vol.36, Part Russian) 2, pp.361‐385 Sereno Paul C., 1986 Phylogeny of the Bird‐hipped Wiman C. (1929) Die Kreide Dinosaurier aus Shantung. Dinosaurs (Order Ornithischia) National : Hadrosauridae: sinensis Geographic Research 2(2); 234‐256 Palaeontologia Sinica, Series C, Vol.VI, Fascicle Taquet (1976) Géologie et Paléontologie du Gisement 1 de Gadoufaoua (Aptien du Niger). Cahiers de Young C.C. (1958) [The dinosaurian remains of Laiyang, Paléontologie. Éditions du Centre National de la Shantung]. Palaeontol. Sinica, ser. C, 16: 1‐138. Recherche Scientifique, Paris. Pp. 1–191. (In Chinese)

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