A review of the basal tyrannosauroids (Saurischia: Theropoda) of the Jurassic Period

Similar documents
Pre-Archaeopteryx coelurosaurian dinosaurs and their implications for understanding avian origins

Dilong Paradoxus. (DIE-long) Early Tyrannosaurid Found in the Middle Jurassic to the Early Cretaceous. Claudia Montilla

Geo 302D: Age of Dinosaurs. LAB 7: Dinosaur diversity- Saurischians

A large theropod metatarsal from the upper part of Jurassic Shishugou Formation in Junggar Basin, Xinjiang, China

Discerning Tyrants from Usurpers: A Statistical Baraminological Analysis of Tyrannosauroidea Yielding the First Dinosaur Holobaramin

DINOSAUR DIVERSITY ANALYSED BY CLADE, AGE, PLACE AND YEAR OF DESCRIPTION

The Origin of Birds. Technical name for birds is Aves, and avian means of or concerning birds.

Origin and Evolution of Birds. Read: Chapters 1-3 in Gill but limited review of systematics

Theropod Teeth from the Middle-Upper Jurassic Shishugou Formation of Northwest Xinjiang, China

Gradual Assembly of Avian Body Plan Culminated in Rapid Rates of Evolution across the Dinosaur-Bird Transition

Stuart S. Sumida Biology 342. (Simplified)Phylogeny of Archosauria

Cladistics (reading and making of cladograms)

Origin and Evolution of Birds. Read: Chapters 1-3 in Gill but limited review of systematics

An Archaeopteryx-like theropod dinosaur newly

Title: Phylogenetic Methods and Vertebrate Phylogeny

Report. Gradual Assembly of Avian Body Plan Culminated in Rapid Rates of Evolution across the Dinosaur-Bird Transition

Juehuaornis gen. nov.

A new large bodied theropod dinosaur from the Middle Jurassic of Warwickshire, United Kingdom

Chase Brownstein, Research Associate, Department of Collections & Exhibitions

University of Bristol - Explore Bristol Research. Early version, also known as pre-print

A new carnosaur from Yongchuan County, Sichuan Province

Brief report. Origin attachments of the caudofemoralis longus muscle in the Jurassic dinosaur Allosaurus. Introduction. ANDREA CAU and PAOLO SERVENTI

Geo 302D: Age of Dinosaurs LAB 4: Systematics Part 1

Burgess Shale ~530 Ma. Eukaryotic Organisms. Pikaia gracilens. Chordates. first chordate? Vertebrates

Jurassic Food Web. Early Childhood Learning Objective

Name: GEOL 104 Dinosaurs: A Natural History Video Assignment. DUE: Wed. Oct. 20

A bizarre Jurassic maniraptoran from China with elongate ribbon-like feathers

Barney to Big Bird: The Origin of Birds. Caudipteryx. The fuzzy raptor. Solnhofen Limestone, cont d

With original illustrations by Brian Regal, Tarbosaurus Studio. A'gJ" CAMBRIDGE UNIVERSITY PRESS

Outline 17: Reptiles and Dinosaurs

Dinosaur Safari Junior. Introduction:

From Dinosaurs to Birds: Puzzles Unraveled while Evidence Building up

Red Eared Slider Secrets. Although Most Red-Eared Sliders Can Live Up to Years, Most WILL NOT Survive Two Years!

Are the dinosauromorph femora from the Upper Triassic of Hayden Quarry (New Mexico) three stages in a growth series of a single taxon?

Modern Evolutionary Classification. Lesson Overview. Lesson Overview Modern Evolutionary Classification

Giant croc with T. rex teeth roamed Madagascar

Edinburgh Research Explorer

Species: Panthera pardus Genus: Panthera Family: Felidae Order: Carnivora Class: Mammalia Phylum: Chordata

CLADISTICS Student Packet SUMMARY Phylogeny Phylogenetic trees/cladograms

Introduction to phylogenetic trees and tree-thinking Copyright 2005, D. A. Baum (Free use for non-commercial educational pruposes)

The Fossil Record of Vertebrate Transitions

Bio 1B Lecture Outline (please print and bring along) Fall, 2006

Modern taxonomy. Building family trees 10/10/2011. Knowing a lot about lots of creatures. Tom Hartman. Systematics includes: 1.

THE FAUNA OF THE ARUNDEL FORMATION OF

University of Bristol - Explore Bristol Research

The Triassic Transition

GEOL 104 Dinosaurs: A Natural History Homework 6: The Cretaceous-Tertiary Extinction. DUE: Fri. Dec. 8

Dinosaur Safari Junior: A Walk in Jurassic Park ver060113

BEHAVIORAL AND PALEOENVIRONMENTAL IMPLICATIONS OF REPTILE SWIM TRACKS FROM THE EARLY TRIASSIC OF WESTERN NORTH AMERICA

Christian Foth 1,2*, Oliver W. M. Rauhut 1,2,3. Introduction. Abstract

oxfitates }Ji2zercanAuseum The Triassic Dinosaur Genera Podokesaurus and Coelophysis BY EDWIN H. COLBERT'

Accepted Manuscript. News & Views. Primary feather vane asymmetry should not be used to predict the flight capabilities of feathered fossils

THE SMALL THEROPOD DINOSAURS TUGULUSAURUS AND PHAEDROLOSAURUS FROM THE EARLY CRETACEOUS OF XINJIANG, CHINA

What is a dinosaur? Reading Practice

1 EEB 2245/2245W Spring 2014: exercises working with phylogenetic trees and characters

Tuesday, December 6, 11. Mesozoic Life

History, New York, USA b Department of Biological Sciences, George Washington University, Washington, DC, USA

A Jurassic ceratosaur from China helps clarify avian digital homologies

8/19/2013. Topic 5: The Origin of Amniotes. What are some stem Amniotes? What are some stem Amniotes? The Amniotic Egg. What is an Amniote?

Article. A new dromaeosaurid (Dinosauria: Theropoda) from the Upper Cretaceous Wulansuhai Formation of Inner Mongolia, China

Evolution of Birds. Summary:

A short look at the early mammals will follow, before examining the demise of the dinosaurs in the K-T Event.

Supporting Information

Carnivore An animal that feeds chiefly on the flesh of other animals.

A juvenile coelurosaurian theropod from China indicates arboreal habits

The early fossil record of dinosaurs in North America: a new neotheropod from the base of the Dockum Group (Upper Triassic) of Texas

INQUIRY & INVESTIGATION

Differences between Reptiles and Mammals. Reptiles. Mammals. No milk. Milk. Small brain case Jaw contains more than one bone Simple teeth

Natural Sciences 360 Legacy of Life Lecture 3 Dr. Stuart S. Sumida. Phylogeny (and Its Rules) Biogeography

Line 136: "Macroelongatoolithus xixiaensis" should be "Macroelongatoolithus carlylei" (the former is a junior synonym of the latter).

Eoraptor: Discovery, Fossil Information, Phylogeny, and Reconstructed Life

Abstract. Troodon is a relatively small, bird-like dinosaur known from the Campanian age

Fossils explained 27: Theropod dinosaurs

A new clade of archaic large-bodied predatory dinosaurs (Theropoda: Allosauroidea) that survived to the latest Mesozoic

Supplementary Figure 1. Comparisons of the holotypes of Alioramus altai and Qianzhousaurus sinensis illustrating selected features that exhibit a

A taxonomic and phylogenetic re-evaluation of Therizinosauria (Dinosauria: Maniraptora)

Edinburgh Research Explorer

Lecture 11 Wednesday, September 19, 2012

Fossils Test Holt 2016 Answer Key. Test Key

Erycine Boids from the Early Oligocene of the South Dakota Badlands

Biologist Ben Garrod has lived with chimpanzees, sharks and polar bears and is proud to be a geek.

SUPPLEMENTARY INFORMATION

Living Dinosaurs (3-5) Animal Demonstrations

In North America 1. the Triassic is represented by the thick Newark Group along the east coast, 2. by widespread red-bed and fluvial sediments in the

Video Assignments. Microraptor PBS The Four-winged Dinosaur Mark Davis SUNY Cortland Library Online

On the Discovery of the earliest fossil bird in China (Sinosauropteryx gen. nov.) and the origin of birds

PRELIMINARY REPORT ON A CLUTCH OF SIX DINOSAURIAN EGGS FROM THE UPPER TRIASSIC ELLIO T FORMATION, NORTHERN ORANGE FREE STATE. J. W.

UNIT III A. Descent with Modification(Ch19) B. Phylogeny (Ch20) C. Evolution of Populations (Ch21) D. Origin of Species or Speciation (Ch22)

SUPPLEMENTARY INFORMATION

1ox4tatre. XJiiie'icanJ/useum. Relationships of the Saurischian Dinosaurs BY EDWIN H. COLBERT1

First Flightless Pterosaur

Introduction to Cladistic Analysis

Dinosaur Safari Junior: A Walk in Jurassic Park

CURRICULUM VITAE SIMON SCARPETTA (July 2018)

.56 m. (22 in.). COMPSOGNATHOID DINOSAUR FROM THE. Medicine Bow, Wyoming, by the American Museum Expedition

POEKILOPLEURON BUCKLANDII, THE THEROPOD DINOSAUR FROM THE MIDDLE JURASSIC (BATHONIAN) OF NORMANDY

Preliminary results on the stratigraphy and taphonomy of multiple bonebeds in the Triassic of Algarve

DINOSAURS. Facts for Students. Introduction to the early world. Types of dinosaurs.

Evolution of Tetrapods

muscles (enhancing biting strength). Possible states: none, one, or two.

Transcription:

VOLUMINA JURASSICA, 2016, XIV: 159 164 DOI: A review of the basal tyrannosauroids (Saurischia: Theropoda) of the Jurassic Period Changyu YUN Key words: tyrannosauroid, Saurischia, theropod, Jurassic Abstract. The well supported clade Tyrannosauroidea represents one of the most basal coelurosaurian theropods. Given that current fossil records of earliest coelurosaur theropods are extremely scarce, basal-most tyrannosauroid materials are key to understanding the origin and diversification of coelurosaurs. Here, I present a brief overview of currently known basal tyrannosauroids of Jurassic age, discussing their systematics and distribution. The currently oldest known Jurassic tyrannosauroids are from Europe continent, possibly suggesting the European origin of the superfamily. INTRODUCTION The Coelurosauria is the only dinosaurian clade which survives today as birds, and it is one of the most diverse theropod clades comprising many herbivorous and carnivorous taxa. Therefore, the diversification of the Coelurosauria is one of the most interesting subject of the evolutionary history of the dinosaurs. Unfortunately, most of the oldest known coelurosaurian fossils are largely fragmentary so it is currently very dificult to understand the clade s diversification. One putative record from the Early Jurassic of China might be the oldest known therizinosaurian (Zhao, Xu, 1998; Barrett, 2009) but its exact age and taxonomic status are controversial (Kirkland, Wolfe, 2001; Kirkland et al., 2005). The Tyrannosauroidea is considered as a basal-most clade of Coelurosauria by a majority of recent phylogenetic analyses (e.g. Loewen et al., 2013; Brusatte et al., 2014) but some analyses found them to be more derived than the Compsognathidae (e.g. Rauhut et al., 2010; Novas et al., 2013). What is clear is that the tyrannosauroids represent a clade close to the origin of the Coelurosauria. Therefore the oldest tyrannosauroid material plays an important role in understanding coelurosaurian origin and diversification. This paper aims to present a review of the currently known Jurassic tyrannosauroids, and a general description of each taxon or subclade. My hope is that this paper will be a helpful guide to understanding tyrannosauroid or coelurosaurian origin and/or distribution. POSSIBLE CASES Iliosuchus incognitus (Huene, 1932) Age: Middle Bathonian, Middle Jurassic Occurrence: Stonesfield Slate, England Comments: Only 3 small ilia are the currently known material of this taxon. Though this material is very small in size (being 9 to 10 cm long), a vertical iliac ridge is clearly present similar to other tyrannosauroids. So this taxon was traditionally allied with the tyrannosauroids (Galton, 1976), though the fact that some other theropods belonging to the 1 Vertebrate Paleontological Institute of Incheon, Incheon 21974, Republic of Korea, Biological Sciences, Inha University, Incheon 22212, Republic of Korea; e-mail: changyu1015@naver.com.

160 C. YUN Tetanurae such as Megalosaurus or Piatnitzkysaurus have similar feature makes this referral uncertain (Benson, 2009). Recent studies have considered Iliosuchus to be an indeterminate avetheropod or a juvenile Megalosaurus (Benson, 2009; Carrano et al., 2012) but such fragmentary material is not enough for accurate classification. If Iliosuchus is indeed a tyrannosauroid, it would be the earliest genus in the clade or maybe even in the whole Coelurosauria itself (Rauhut, 2003). Coeluridae (Marsh, 1881) Definition: The most inclusive clade containing Coelurus fragilis but not Proceratosaurus bradleyi, Tyrannosaurus rex, Allosaurus fragilis, Compsognathus longipes, Ornithomimus edmontonicus and Deinonychus antirrhopus (Hendrickx et al., 2015) Comments: Whether or not this clade is monophyletic is controversial, and some taxon or whole members of the clade might not belong to the Tyrannosauroidea at all (Choiniere et al., 2014). Many of the recent analyses found that this clade belongs to the basal tyrannosauroids (e.g. Senter, 2007; Brusatte et al., 2014). There are currently two genera in this clade, which are Coelurus and Tanycolagreus. This clade comprises small carnivorous coelurosaurs which are likely have hunted small prey. Coelurus fragilis (Marsh, 1879) Age: Middle, Late Kimmeridgian, Late Jurassic Occurrence: Morrison Formation, Wyoming, USA Comments: The exact position of this taxon s theropoda phylogenetical tree is uncertain. Some consider Coelurus as more derived than the tyrannosauroids (Turner et al., 2007), or even than the basal maniraptoran (Zanno, 2010). If this taxon indeed forms a clade Coeluridae and belongs to the tyrannosauroid, it is probably close to the base (Senter, 2007). This taxon had a relatively long neck and trunk, and a long slender hindlimb. This suggests it was a small, gracile theropod with great speed ability. Tanycolagreus topwilsoni (Carpenter et al., 2005) Age: Middle, Late Kimmeridgian, Late Jurassic Occurrence: Morrison Formation, Wyoming, USA Comments: This taxon could be synonymous with the tyrannosauroid Stokesosaurus clevelandi, since they are similar sized coelurosaurs from the same geological formation. However, the ilium of Tanycolagreus is currently unknown so the direct comparison of the taxa is currently impossible (the distinctive bones of Stokesosaurus being the ilia). If this taxon indeed forms the clade Coeluridae and belongs to the tyrannosauroid, it is probably close to the base (Senter, 2007). The taxon had a large, enlongated skull and long legs, and gracile general morphology. CERTAIN CASES Proceratosauridae (Averianov et al., 2010) Definition: A node based taxon including Proceratosaurus bradleyi and Kileskus aristotocus, their most recent common ancestor and all its decendants (Averianov et al., 2010). Comments: Rauhut et al. (2010) first suggested the definition for the Proceratosauridae as all theropods that are more closely related to Proceratosaurus than to Tyrannosaurus, Allosaurus, Compsognathus, Coelurus, Ornithomimus, or Deinonychus. Averianov et al. (2010) pointed out that this definition suggested by Rauhut et al. (2010) does not meet ICZN s requirements, so their Proceratosauridae is a nomen nudum. There are currently 5 valid taxa belong to this clade, based on the parsimony analysis of Brusatte, Carr (2016) and 3 of them are from the Jurassic period. This clade comprises small to large basal tyrannosauroids (Brusatte, Carr, 2016) characterized by crests on their head. Since the crests of these dinosaurs are thin, they might have served as display organs. Guanlong wucaii (Xu et al., 2006) Age: Oxfordian, Late Jurassic Occurrence: Shishugou Formation, Xinjiang, China Comments: This is a taxon famous for its highly distinctive crest on its skull (Fig. 1A). Carr (2006) suggested that this taxon is actually a Carnosauria sister to Monolophosaurus or even possibly synonymous with it. This was supported by Paul (2010) as he described this taxon as Monolophosaurus wucaii. However, no other analyses have found them as closely related (e.g. Loewen et al., 2013; Brusatte, Carr, 2016). As this taxon had long forelimbs with a large manus and a small skull with small teeth, it is likely that its forelimbs played an important role in hunting unlike the more derived tyrannosauroids, as their forelimbs are very shortened.

A review of the basal tyrannosauroids (Saurischia: Theropoda) of the Jurassic Period 161 A. Guanlong. B. Proceratosaurus. Reconstructions by Tracy Ford Fig. 1. Skull reconstructions of the two Jurassic proceratosaurids Proceratosaurus bradleyi (Woodward, 1910; Huene, 1926) Age: Middle Bathonian, Middle Jurassic Occurrence: Great Oolite, England Comments: Once considered as a taxon closely related to Ceratosaurus (Huene, 1926), this is now considered as the currently oldest definite tyrannosauroid and coelurosaur of all time (Rauhut et al., 2010). The currently only known skull has a small horn on the end of its snout, but this is probably the trace of a broken delicate crest similar that present in Guanlong (Rauhut et al., 2010; Fig. 1B). It had a small, subrectangular head and it probably had a similar lifestyle to Guanlong. Kileskus aristotocus (Averianov et al., 2010) Age: Bathonian, Middle Jurassic Occurrence: Itat Formation, Russia Comments: This is only known from very fragmentary cranial material, but this is very similar to Proceratosaurus. This is one of the most basal coelurosaur and tyrannosauroid genera, and one of the oldest records of these clades. This taxon probably hunted small vertebrates such as fishes, salamanders, turtles or lizards which are widely known in the Itat Formation (Averianov et al., 2010). Primitive Tyrannosauroidea Comments: These genera are placed in between the Proceratosauridae and the Tyrannosauridae. It is still possible that some taxa belong to primitive clades like Proceratosauridae or Coeluridae. There are currently 3 taxa known from the Jurassic Period (Brusatte, Carr, 2016). Aviatyrannis jurassica (Rauhut, 2003) Age: Early Kimmeridgian, Late Jurassic Occurrence: Alcobaca Formation, Portugal Comments: This is one of the oldest tyrannosauroids ever found. The holotype ilium was once originally referred to Stokesosaurus, though later study described it as a new genus (Rauhut, 2003). However, it is probable that this genus is in fact a Portuguese species of Stokesosaurus. Some material such as an ilium (now lost) and an isolated tooth from the North American Morrison Formation were once referred to Stokesosaurus, but might actually belong to Aviatyrannis (Rauhut, 2003). These findings, and the cases of Portuguese Allosaurus or Torvosaurus (Mateus et al., 2006), support the Kimmeridgian land connections between North America and Europe. Juratyrant langhami (Benson, 2008; Brusatte, Benson, 2013) Age: Early Tithonian, Late Jurassic Occurrence: Kimmeridge Clay, England Comments: Once thought to be a species of Stokesosaurus, later study found this taxon to be a new genus of tyrannosauroid. A 2013 analysis found the taxon to be closely related to Eotyrannus (Brusatte, Benson, 2013) but later analyses support a close relationship with Stokesosaurus (e.g. Loewen et al., 2013). Juratyrant and Stokesosaurus once thought to be as derived Proceratosauridae (Loewen et al., 2013) but later analyses found no support for this classification (e.g. Brusatte, Carr, 2016). This taxon was quite larger than Stokesosaurus, as the preserved ilium was more than twice as big as the Stokesosaurus holotype (Fig. 2A).

162 C. YUN A. Stokesosaurus. B. Juratyrant. Modified from Brusatte, Benson (2013) Fig. 2. Comparison of the two ilia of different Jurassic tyrannosauroids Stokesosaurus clevelandi (Madsen, 1974) Age: Middle, Late Kimmeridgian, Late Jurassic Occurrence: Morrison Formation, South Dakota, USA Comments: Even though material belonging to several specimens has been referred to this taxon, the only certain material is the holotype ilium (Fig. 2B). Some material referred to this taxon may be Aviatyrannis. The genus once had an English species Stokesosaurus langhami, but this taxon was recently described as the new genus Juratyrant (Brusatte, Benson, 2013). Stokesosaurus and Juratyrant once thought to be derived Proceratosauridae (Loewen et al., 2013) but later analyses found no support for this classification (e.g. Brusatte, Carr, 2016). DISCUSSION There are currently 6 certain cases of Jurassic tyrannosauroids, and this becomes 9 when possible cases are included. At least 3 taxa are from the European continent, this being about 50% of the current diversity. When possible cases are included, 4 taxa are from Europe and this is approximately 44% of current cases. This strongly suggests the European origin of the tyrannosauroids, and the currently known oldest tyrannosauroid taxa (Proceratosaurus, possibly Iliosuchus) are found in Europe. The fact that North America and Europe were connected in the Late Jurassic further supports this hypothesis. However, with the current state of the lack of enough tyrannosauroid material from the Jurassic, this is still not certain. But the abundance of basal, Jurassic tyrannosauroid material from Eurasia indicates they are originated at least in Eurasia.

A review of the basal tyrannosauroids (Saurischia: Theropoda) of the Jurassic Period 163 The question of where and when the clade Coelurosauria originated, and diversified remains uncertain. Eshanosaurus from the Lufeng Formation of China is Early Jurassic in age, and the possibility that Eshanosaurus might be a derived therizinosaurian could suggest that the coelurosaurs might have originated and diversified long before that (Xu et al., 2001). However, this taxon still could be a basal Sauropodomorpha convergent with the therizinosaurs (Kirkland, Wolfe, 2001) so this is yet to be certain. Given the fact that the tyrannosauroids are largely considered as the basal-most coelurosaurian clade (e.g. Loewen et al., 2013; Brusatte et al., 2014), the diversification or the origin of the coelurosaurs could be inferred from Jurassic tyrannosauroids. Proceratosaurus is the definite oldest coelurosaur known as today (Rauhut et al., 2010), so it is possible that the whole Coelurosauria clade originated in Europe, or at least Eurasia. However later, detailed studies of the exact age and systematic position of Eshanosaurus, or futu re discoveries of basal coelurosaurs, will make this issue clear. Acknowledgements. I thank Thomas Holtz, and Thomas Carr for kindly discussing the evolutionary history of the tyrannosauroids with me. Discussions with J.Y. Park, Y.W. Lee, B.H. Ji about coelurosaur radiation were also helpful. I thank all these people. My special thank goes to Mickey Mortimer, whose excellent database of theropod information helped this study a lot. I am particularly thankful of Tracy Ford for allowing me to use his skull reconstructions. REFERENCES AVERIANOV A.O., KRASNOLUTSKII S.A., IVANTSOV S.V., 2010 A new basal coelurosaur (Dinosauria: Theropoda) from the Middle Jurassic of Siberia. Proceedings of the Zoological Institute. 314, 1: 42 57. BARRETT P.M., 2009 The affinities of the enigmatic dinosaur Eshanosaurus deguchiianus from the Early Jurassic of Yunnan Province, People s Republic of China. Palaeontology, 52, 4: 681 688. BENSON R.B.J., 2009 An assessment of variability in theropod dinosaur remains from the Bathonian (Middle Jurassic) of Stonesfield and New Park Quarry, UK and taxonomic implications for Megalosaurus bucklandii and Iliosuchus incognitus. Palaeontology, 52: 857 877. BRUSATTE S.L., BENSON R.B.J., 2013 The systematics of Late Jurassic tyrannosauroids (Dinosauria: Theropoda) from Europe and North America. Acta Palaeontologica Polonica, 58, 1: 47 54. BRUSATTE S.L., CARR T.D., 2016 The phylogeny and evolutionary history of tyrannosauroid dinosaurs. Scientific Reports, 6, 20252. BRUSATTE S.L., LLOYD G.T., WANG S.C., NORELL M.A., 2014 Gradual assembly of avian body plan culminated in rapid rates of evolution across the dinosaur-bird transition. Current Biology, 24, 20: 2386 2392. CARPENTER K., MILES C., CLOWARD K., 2005 New small theropod from the Upper Jurassic Morrison Formation of Wyoming. In: The Carnivorous Dinosaurs (ed. K. Carpenter): 23 48. Indiana University Press, Bloomington. CARR T., 2006 Is Guanlong a tyrannosauroid or a subadult Monolophosaurus? Journal of Vertebrate Paleontology. 26: 48A. CARRANO M.T., BENSON R.B.J., SAMPSON S.D., 2012 The phylogeny of Tetanurae (Dinosauria: Theropoda). Journal of Systematic Palaeontology, 10, 2: 211 300. CHOINIERE J.N., CLARK J.M., FORSTER C.A., NORELL M.A., EBERTH D.A., ERICKSON G.M., CHU H., XU X., 2014 A juvenile specimen of a new coelurosaur (Dinosauria: Theropoda) from the Middle-Late Jurassic Shishugou Formation of Xinjiang, People s Republic of China. Journal of Systematic Palaeontology, 12, 2: 177 215. GALTON P.M., 1976 Iliosuchus, a Jurassic dinosaur from Oxfordshire and Utah. Palaeontology, 19, 3: 587 589. HENDRICKX C., HARTMAN S.A., MATEUS O., 2015 An overview of non-avian theropod discoveries and classification. PalArch s Journal of Vertebrate Palaeontology, 12, 1: 1 73. HUENE F.V., 1926 On several known and unknown reptiles of the order Saurischia from England and France. Annals and Magazine of Natural History, 9.17, 101: 473 489. HUENE F.V., 1932 Die fossile Reptil-Ordnung Saurischia, ihre Entwicklung und Geschichte. Monographien zur Geologie und Palaeontologie, serie 1, 4, 1/2: 1 361. KIRKLAND J.I., WOLFE D.G., 2001 First definitive therizinosaurid (Dinosauria: Theropoda) from North America. Journal of Vertebrate Paleontology, 21, 3: 410 414. KIRKLAND J.I., ZANNO L.E., SAMPSON S.D., CLARK J.M., DEBLIEUX D.D., 2005 A primitive therizinosauroid dinosaur from the Early Cretaceous of Utah. Nature, 435, 7038: 84 87. LOEWEN M.A., IRMIS R.B., SERTICH J.J.W., CURRIE P.J., SAMPSON S.D., 2013 Tyrant Dinosaur Evolution Tracks the Rise and Fall of Late Cretaceous Oceans. PLoS ONE, 8, 11: e79420. MARSH O.C., 1879 Notice of new Jurassic reptiles. American Journal Science, 18: 501 505. MARSH O.C., 1881 A new order of extinct Jurassic reptiles (Coeluria). American Journal Science, 21: 339 341. MADSEN J.H., 1974 A new theropod dinosaur from the Upper Jurassic of Utah. Journal of Paleontology, 48: 27 31. MATEUS O, WALEN A, ANTUNES M.T., 2006 The large theropod fauna of the Lourinha Formation (Portugal) and its similarity to that of the Morrison Formation, with a description of a new species of Allosaurus. In: Paleontology and Geology of the Upper Jurassic Morrison Formation (eds J.R. Foster, S.G. Lucas): 123 129. New Mexico Museum of Natural History and Science Bulletin, 36. Albuquerque, New Mexico. NOVAS F.E., AGNOLIN F.L., EZCURRA M.D., PORFIRI J., CANALE J.I., 2013 Evolution of the carnivorous dinosaurs during the Cretaceous: The evidence from Patagonia. Cretaceous Research, 45: 174 215.

164 C. YUN PAUL G.S., 2010 The Princeton Field Guide to Dinosaurs. Princeton University Press. 320 pp. RAUHUT O.W.M., 2003 A tyrannosauroid dinosaur from the Upper Jurassic of Portugal. Palaeontology, 46, 5: 903 910. RAUHUT O.W.M., MILNER A.C., MOORE-FAY S., 2010 Cranial osteology and phylogenetic position of the theropod dinosaur Proceratosaurus bradleyi (Woodward, 1910) from the Middle Jurassic of England. Zoological Journal of the Linnean Society, 158: 155 195. SENTER P., 2007 A new look at the phylogeny of Coelurosauria (Dinosauria: Theropoda). Journal of Systematic Paleontology, 5, 4: 429 463. TURNER A.H., POL D., CLARKE J.A., ERICKSON G.M., NORELL M.A., 2007 A basal dromaeosaurid and size evolution preceding avian flight. Science, 317: 1378 1381. WOODWARD A.S., 1910 On a skull of Megalosaurus from the Great Oolite of Minchinhampton (Gloucestershire). Quarterly Journal of the Geological Society. 66: 111 115. XU X., ZHAO X., CLARK J.M., 2001 A new therizinosaur from the Lower Jurassic Lower Lufeng Formation of Yunnan, China. Journal of Vertebrate Paleontology, 21, 3: 477 483. XU X., CLARK J.M., FORSTER C.A., NORELL M.A., ERICK- SON G.M., EBERTH D.A., JIA C., ZHAO Q., 2006 A basal tyrannosauroid dinosaur from the Late Jurassic of China. Nature, 439, 7077: 715 718. ZANNO L.E., 2010 A taxonomic and phylogenetic review of Therizinosauria. Journal of Systematic Palaeontology, 8: 503 543. ZHAO X., XU X., 1998 The oldest coelurosaurian. Nature, 394, 6690: 234 235.