The Lossiemouth Sandstone Formation of Scotland

            The yellowish sandstone of the Lossiemouth Sandstone Formation can be found on the coast near Elgin, in the Moray council area, north east of Scotland (Fig 1). Fossils were collected there in different quarries, around the town of Lossiemouth, at the end of the 19th and beginning of the 20th century, notably by the ardent collector William Taylor of Lhanbryde (1849-1921). The sand from the sandstone was probably carried by wind and deposited over a fluvial area, indicating that the location during the Late Triassic was a sand dune desert with narrow strips of lowland vegetation around rivers. The sandstone did not preserve any index fossil such as pollens, plants or invertebrates, and no radiometric dating could be performed, leading to some uncertainties on the exact age of the rocks. However, based on the correlation of the Lossiemouth vertebrate fauna with those of the Maleri Formation of India, the Santa Maria Formation of Brazil, the Ischigualasto Formation of Argentina, a Late Carnian age is generally attributed to the sandstone. The fauna is represented by eight taxa of reptiles, including six archosaurs.

Fig. 1.- Location of the Lossiemouth Sandstone Formation today (left) and during the Late Triassic (right).

Saltopus elginensis Huene, 1910 ("Elgin's hopping foot"), is known from a single badly preserved skeleton. The exact affinity of this small (60 cm long) bipedal predator has been debated for decades. It was at some point classified as an early theropod dinosaur but more recent analysis put it within the dinosauriformes but outside the Dinosauria clade as a sister taxon to them (It means Saltopus is not a dinosaur but one of its closest relatives). Since the skull in the fossil is missing, the diet of this animal is unknown.

Another interesting animal from the Carnian of Scotland is Scleromochlus taylori Woodward, 1907 ("Taylor's hard fulcrum") (Fig 2). This rather strange 1.8 m long creature looks a bit like a lizard on long slender legs. It was related or even has been considered ancestral to the pterosaurs, a group of archosaurs that will eventually  conquer the air. Several skeletons of this animal are known.

Fig 2.- Reconstruction of Scleromochlus taylori.

The 4 meter long and probable top predator of its time, Ornithosuchus longidens ("long-toothed bird crocodile") (Huxley, 1877) (Fig. 3) belongs to another group of facultative bipedal carnivorous reptiles distantly related to crocodiles, the Ornithosuchians. They were equipped with sharp teeth and a row of bony scales (osteoderms) along their back and tail. Ornithosuchus was once thought to be ancestral to the theropod dinosaurs, but details of its skeletal anatomy such as the braincase and the configuration of the ankle show that it was a Crurotarsi like the Rauisuchians, the Aetosaurs, crocodiles and phytosaurs and not an Avemetatarsalia (Dinosaurs and Pterosaurs).

Fig. 3- Reconstruction of Ornithosuchus longidens.

Erpetosuchus granti Newton, 1894 ("Grant's Snake Crocodile") was a small (60 cm long) agile quadrupedal predator that might have hunted small lizards and amphibians (Fig 4). Erpetosuchus was the Lossiemouth fossil the most closely related to modern crocodiles and is known from at least four specimens. Considering the location of Scotland at that time (Fig 1), it is no surprise that an additional fossil referable to the same animal was discovered in the New Haven Formation of Connecticut, United States.

Fig. 4.- Reconstruction of Erpetosuchus granti.

Herbivores are represented by several groups of reptiles. The rhynchosaurs had stocky bodies with a broad skull and a powerful beak. They may have fed on tough vegetation, such as the seed ferns which were abundant at that time. In Europe, Rhynchosaurs were represented by the 1.3 meter long  Hyperodapedon gordoni Huxley, 1859 ("Gordon's best pestle tooth") from Scotland (Fig. 5). It is known from at least 35 individuals, making it the most abundant vertebrate fossils of the formation. The fossils came into various sizes, reflecting ages, that can be grouped into two general types (morphotypes) possibly indicating sexual dimorphism. The genus Hyperodapedon had a worldwide distribution, with several species described from India, Brazil, Argentina. Zimbabwe, Madagascar, Tanzania and the United states. They had therefore been used to correlate different formations across the globe, serving as an "index" fossil.

Fig. -5. - A pair of Hyperodapedon gordoni.

Aetosaurs were heavily armored  archosaurs, with a body covered with plate-like scutes (osteoderms) and spikes. These vegetarian animals were also distantly related to crocodiles and are now thought to have been fully terrestrial animals. The carnian representives in Europe include the genera Stagonolepis and Paratypothorax, with Stagonolepis robertsoni Agassiz, 1884 ("Robertson's pitted scale") being the Lossiemouth species (Fig. 6). It measured about 3 meters in length. The remains of Stagonolepis were originally mistaken for fish scales, thus the generic name.

Fig. 6.- Stagonolepis robertsoni.

Procolophonids were small lizard like creatures belonging to the ancient lineage of reptiles called Parareptilia. By the end of the Triassic they have adopted a vegetarian diet before being wiped out by extinction at the end of the period. Leptopleuron lacertinum Owen, 1851 ("Lizard slender ribs") is a typical procolophonid that measured about 30 cm in length (Fig 7). It might have lived in burrows. This little critter was the subject of a bitter rivalry between famed paleontologists Richard Owen and Gideon Mantell at the end of the 19th century, both wanting to be first to describe the animal. Mantell christened the fossil Telerpeton elginense but Owen was quicker to publish so the name he gave has priority according to the international rules of nomenclature.

Fig. 7.- Reconstruction of Leptopleuron lacertinum.

The rhynchocephalians (and more restrictively, the sphenodontians) were once a successful and diverse group of lizard-like mesozoic reptiles with both aquatic and terrestrial forms. The only modern surviving member of the rhynchocephalians is the tuatara (Sphenodon) from New Zealand, generally presented as a true "living fossil". The Lossiemouth sandstone has yielded the species Brachyrhinodon taylori Huene, 1910 ("Taylor's short nose teeth") (Fig. 8) which was very similar to the tuatara in shape, but smaller, measuring some 25 cm in length, and with probably a similar lifestyle. Both Leptopleuron and Brachyrhinodon are known from numerous specimens.

Fig -8.- Reconstruction of Brachyrhinodon taylori.

All artworks on this page are copyrighted to Nobu Tamura. Do not use without permission. Contact: nobu dot tamura at yahoo dot com.

References:

Benton, M. (1983). The Triassic reptile Hyperodapedon from Elgin: functional morphology and relationships. Phil. Trans. R. Soc. Lond. B, 302(1112), 605–718.

Benton, M. (1999). Scleromochlus taylori and the origin of dinosaurs and pterosaurs. Phil. Trans. R. Soc. Lond. B, 354, 1423–1446.

Benton, M., & Walker, A. (2002). Erpetosuchus, a crocodile-like basal archosaur from the Late Triassic of Elgin, Scotland. Zoological Journal of the Linnean Society, 136, 25–47.

Benton, M. J., & Walker, A. D. (2011). Saltopus, a dinosauriform from the Upper Triassic of Scotland. Earth and Environmental Science Transactions of the Royal Society of Edinburgh, 101(3-4), 285–299.

Fraser, N. C., & Benton, M. J. (1989). The Triassic reptiles Brachyrhinodon and Polysphenodon and the relationships of the sphenodontids. Zoological Journal of the Linnean Society, 96(4), 413–445.

Olsen, P. E., Sues, H.-D., & Norell, M. A. (2000). First record of Erpetosuchus (Reptilia: Archosauria) from the Late Triassic of North America. Journal of Vertebrate Paleontology, 20(4), 633–636.

Säilä, L. K. (2010). Osteology of Leptopleuron lacertinum Owen, a procolophonoid parareptile from the Upper Triassic of Scotland, with remarks on ontogeny, ecology and affinities. Earth and Environmental Science Transactions of the Royal Society of Edinburgh, 101(01), 1–25.

Spencer, P. (2000). The braincase structure of Leptopleuron lacertinum Owen (Parareptilia: Procolophonidae). Journal of Vertebrate Paleontology, 20(1), 21–30.

Walker, A. (1961). Triassic reptiles from the Elgin area: Stagonolepis, Dasygnathus and their allies. Phil. Trans. R. Soc. Lond. B, 244(709), 103–204.

Walker, A. (1964). Triassic reptiles from the Elgin area: Ornithosuchus and the origin of carnosaurs. Phil. Trans. R. Soc. Lond. B, 248(744), 53–134.

Watson, D. M. S. (1909). On some Reptilian Remains from the Trias of Lossiemouth (Elgin). Quarterly Journal of the Geological Society, 65(1-4), 440–440.

Woodward, a. S. (1907). On a New Dinosaurian Reptile (Scleromochlus Taylori, gen. et sp. nov.) from the Trias of Lossiemouth, Elgin. Quarterly Journal of the Geological Society, 63(1-4), 140–144.

Sciurumimus albersdoerferi: Is it a girl? Is it a boy? No, it’s a Megalosauroid…

Remember the perfectly preserved complete articulated skeleton of a young dinosaur that was presented to the press last year? Well, the paper describing it has finally been published in the Proceedings of the National Academy of Science. ‘Otto’, also known as the Kelheim theropod,  has now a proper scientific name, Sciurumimus albersdoerferi, the generic name meaning “Squirrel mimic” (in reference to its bushy tail) and the specific name honors Raimund Albersdörfer, who made the specimen available for study.  The fossil was found near Painten, Bavaria (Germany) and dates from the upper Kimmeridgian. Besides the exquisite state of preservation of the fossil that shows evidence of proto-feathers covering at least part of the body, the importance of Sciurumimus stems from its phylogenetic position on the dinosaur evolutionary tree.  It is a megalosauroid, sister taxon to the likes of Megalosaurus, Torvosaurus and Eustreptospondylus, therefore representing the most basal theropod showing direct evidence of feathers, and the most complete megalosauroid remain yet discovered. This raises the interesting possibility that feathers might be a common inherited trait to all theropods and even to all dinosaurs if indeed the feather-like structures found on Tianyulong (an heterodontosaur) and quills on the tail of Psittacosaurus (a Ceratopsian) are analogous structures.

References:

Oliver W. M. Rauhut, Christian Foth, Helmut Tischlinger, and Mark A. Norell (2012) Exceptionally preserved juvenile megalosauroid theropod dinosaur with filamentous integument from the Late Jurassic of Germany, PNAS, Advanced online publication.

Bicentenaria argentina, a new theropod dinosaur from Argentina

Bicentenaria argentina, a new theropod dinosaur from Argentina

Argentina has commemorated the 200th anniversary of its May revolution that led to the country independence on May 25, 2010. Two years later, paleontologists from that country announced the discovery of a new dinosaur and named it after the event, perhaps because the remains were unearthed on that day.  Bicentenaria argentina was unveiled to the public on Tuesday June 26, 2012 through a short press release  with pictures of the mounted skeletons of two fighting individuals (from which my illustration is based on). It is a small theropod that measured about 2.5 meters in length. The paragraph quoted from an interview with lead paleontologist Fernando Novas simply says that Bicentenaria is part of a group of dinosaurs that contain tyrannosaurs and Velociraptor and a distant ancestor to birds. This hints that Bicentenaria is a coelurosaur. The pictures of the mounted skeletons do not tell how much of it is actually known, as people tend nowadays to reconstruct entire skeletons from rather incomplete material. The actual remains consist of some 130 bones from at least 3 adults and several juveniles. The mounts look like those of a generic small size theropod, which probably means that Bicentenaria was a rather basal coelurosaurian, neither a tyrannosauroid, nor a dromaeosaur. However, the press release says the fossil is 90 million year old, thus Late Cretaceous, which seems a bit of a young age for a basal coelurosaur. I could guess the remains were found in the Portezuelo Formation of Turonian age in the Rio Negro Province, which means that Bicentenaria was a contemporary of the fabled Megaraptor, the dromaeosaurs Neuquenraptor and Unenlagia, as well as the alverezsaur Patagonykus. But let’s wait for the formal  publication of the description of this intriguing animal.

Correction: I was just told that Bicentenaria is from the Candeleros Formation of Cenomanian age, therefore a contemporary of Giganotosaurus and Buitreraptor.
 
Original artworks on Paleoexhibit are copyrighted to Nobu Tamura. Do not use without permission (Email: nobu dot tamura at yahoo dot com)

Theropods of the British Isles Part III

Fig 1.- Juratyrant langhami

Late Jurassic Theropods of the British Isles

From the Oxfordian stage (~ 158 MYA), Metriacanthosaurus parkeri (von Huene, 1923) is another obscure tetanuran theropod, known from vertebrae, pelvic and hindlimbs elements (OUM J.12144) found near Weymouth, Dorset in the Oxford Clay Formation. Originally thought to be a megalosaurid, there is a possibility that it actually belongs to a group called sinraptorid, better known by its Chinese representatives such as Sinraptor and Yangchuanosaurus. Metriacanthosaurus probably measured about 8 meters in length.

The Kimmeridge Clay Formation has yielded a few theropod remains: one incomplete tooth from Wiltshire referred to “Megalosaurus” insignis (Eudes-Delongchamps and Lennier vide Lennier, 1870) is from a indeterminate theropod. A tibia (OUM J13568) is possibly from a megalosaur or a tetanuran. Two pedal phalanges of Fleet, Dorset are from a tetanuran.

Fig 2.- Metriacanthosaurus parkeri may have been related to Sinraptor.

Tyrannosauroids are represented by Juratyrant langhami (Benson, 2008) from the Kimmeridge Clay of Tithonian age (~149 MYA). This one is known from a single partial skeleton including a pelvis, partial leg and vertebrae (OUMNH J.3311-1—J.3311-30) found in Dorset. Juratyrant is more closely related to the British Early Cretaceous Eotyrannus than to the North American Stokesosaurus to which the animal was originally referred. Juratyrant measured about 5 meters in length.

References:

R. B. J. Benson. 2008. New information on Stokesosaurus, a tyrannosauroid (Dinosauria: Theropoda) from North America and the United Kingdom. Journal of Vertebrate Paleontology 28(3):732-750

Brusatte, S.L. and Benson, R.B.J. (In press). "The systematics of Late Jurassic tyrannosauroids (Dinosauria: Theropoda) from Europe and North America." Acta Palaeontologica Polonica, (in press).

F. v. Huene. 1923. Carnivorous Saurischia in Europe since the Triassic. Bulletin of the Geological Society of America 34:449-458.

D. Naish and D. M. Martill. 2007. Dinosaurs of Great Britain and the role of the Geological Society of London in their discovery: basal Dinosauria and Saurischia. Journal of the Geological Society, London 164:493-510.

Theropods of the British Isles Part II

 Middle Jurassic Theropods of the British Isles

The Middle Jurassic of England was dominated by Megalosaurids, a family of large primitive tetanuran theropods, now believed to be closely related to the fish-eating Spinosaurids, early representatives of groups that will thrive during the Cretaceous, the tyrannosauroids and the maniraptorans were also present.

Fig 1.- Duriavenator hesperis

The Aalenian-Bajocian stages: Magnosaurus and Duriavenator

The Inferior Oolite formation of Aalenian-Bajocian age (~ 172 MYA) has given a few fragmentary remains of a theropod named Magnosaurus nethercombensis (von Huene, 1923) (originally ‘Megalosaurus’ nethercombensis) and described from partial dentaries, vertebrae, partial ilium, pubis and hindlimb (OUM J12143) found in Nethercomb, Dorset. Various others bits from the same formation in southern England were also referred to this rather obscure tetanuran. The fossil of M. nethercombensis has recently been reevaluated (Benson, 2010) and established to be a valid taxon. This megalosaurid is the oldest known tetanuran.

From the Upper Inferior Oolite Formation of Bajocian age (~ 170 MYA) comes Duriavenator hesperis (Waldman, 1974) (originally Megalosaurus hesperis), known from cranial bones (BMNH R332) found near Sherbourne in Dorset. This is another megalosaurid.

Fig 2.- Megalosaurus bucklandii

The Bathonian stage: Megalosaurus  and Proceratosaurus

The Bathonian age  (~166 MYA) of the British Isles is represented by a handful of theropods. The most famous of them is Megalosaurus, a name coined by William Buckland in 1824 to describe various remains including a lower jaw, vertebrae and partial hindlimbs uncovered at the Stonesfield quarry (Taynton Limestone Formation) that he thought belonged to a giant lizard-like creature. As many of the names from the early days of paleontology, Megalosaurus became a formidable wastebasket taxon, given to an assortment of miscellaneous theropod bones found around the world. Nowadays, only one species, Megalosaurus bucklandii Mantell, 1827 is considered valid and corresponds to the original material described by Buckland. Megalosaurus was a large 9 meter long theropod that was probably the top land predator of its time.

Cruxicheiros newmanorum Benson & Bradley, 2010 from the Chipping Norton Limestone Formation of lower Bathonian age, is based on scant materials, including a partial right femur (WARMS G15770) and other bits found on the same location near Little Crompton, Warwickshire. This one was a basal tetanuran of some sort. A single damaged vertebra found in the same formation but now lost, was named Streptospondylus cuvieri Owen, 1842.

Iliosuchus incognitus von Huene, 1932 from the Taynton Limestone Formation (Bathonian) of Stonesfield, Oxfordshire is known from three small ilia (BMNH R83, OUM J29780 and OUM J28971) found alongside remains of Megalosaurus. It is unclear what it was, either a small megalosaurid or the earliest known tyrannosauroid as some have suggested. A fragmentary small tibia found in the same formation was referred to Iliosuchus as well.

Fig 3.- Proceratosaurus bradleyi

Proceratosaurus bradleyi (Woodward, 1910) from the Great Oolite Group (White Limestone Formation) of Minchinhampon, Gloucestershire (Bathonian) is known from a partial skull exhibiting a nasal horn (which was possibly part of a larger crest), thus the name. This is an early tyrannosauroid, a member of this group of coelurosaurs, which will culminate into the North American Tyrannosaurus rex at the end of the Cretaceous period. Proceratosaurus perhaps measured about 3 meters in length.

From the Forest Marble Formation of Bathonian age, famous for its fossils of the sauropod Cetiosaurus, some troodont-like and dromaeosaur-like teeth have been unearthed, making it the earliest occurrence of this group in the fossil record (Evans & Milner, 1994).

The Callovian stage: Eustreptospondylus

Later in the Middle Jurassic (Callovian stage, ~163 MYA), lived another Megalosaurid named Eustreptospondylus oxoniensis Walker, 1964. This one is known from a partial skull (OUM J13558) and a partial skeleton from a juvenile individual found in Wolvercote, Oxfordshire, at the bottom of the Oxford Clay Formation. This rather obscure species was popularized in one episode of the BBC Series “walking with dinosaurs”. It probably measured something like 5 m in length.

References:

R. B. J. Benson. 2008. A redescription of 'Megalosaurus' hesperis (Dinosauria, Theropoda) from the Inferior Oolite (Bajocian, Middle Jurassic) of Dorset, United Kingdom. Zootaxa 1931:57-67

R. B. J. Benson, 2010, The osteology of Magnosaurus nethercombensis (Dinosauria, Theropoda) from the Bajocian (Middle Jurassic) of the United Kingdom and a re examination of the oldest records of tetanurans, Journal of Systematic Palaeontology, 8(1): 131-146.

S. E. Evans and A. R. Milner. 1994. Middle Jurassic microvertebrate assemblages from the British Isles. In the Shadow of the Dinosaurs: Early Mesozoic Tetrapods, N. C. Fraser and H.-D. Sues (eds.), Cambridge University Press 303-321

F. von Huene, F. 1923. Carnivorous Saurischia in Europe since the Triassic. Bulletin of the Geological Society of America 34:449-458.

D. Naish and D. M. Martill. 2007. Dinosaurs of Great Britain and the role of the Geological Society of London in their discovery: basal Dinosauria and Saurischia. Journal of the Geological Society, London 164:493-510.

R. Sadleir, P. M. Barrett, and H. P. Powell. 2008. The anatomy and systematics of Eustreptospondylus oxoniensis, a theropod dinosaur from the Middle Jurassic of Oxfordshire, England. Monograph of the Palaeontographical Society, London 160(627):1-82

M. Waldman. 1974. Megalosaurids from the Bajocian (Middle Jurassic) of Dorset. Palaeontology 17(2):325-339.

A. D. Walker. 1964. Triassic reptiles from the Elgin area: Ornithosuchus and the origin of carnosaurs. Philosophical Transactions of the Royal Society of London, Series B, Biological Sciences 248:53-134

Theropods of the British Isles Part I

The bipedal theropods represent the most diverse group of dinosaurs including all the meat-eating ones as well as some omnivorous and herbivorous forms. Primitive theropods include the coelophysoids (small, slender and lightly built dinosaurs that thrived worldwide during the Late Triassic, and for which the best known representative is the North American Coelophysis), the ceratosaurs (including forms such as Ceratosaurus and Carnotaurus) and the tetanurans. The last group contains the vast majority of the theropods and its members are characterized among other things by a rigid tail and the total loss of the fourth and fifth digits in their hands. Megalosaurs (i.e. Megalosaurus) are early tetanurans while Spinosaurs (i.e. Spinosaurus and co) are possibly related to them. Later tetanurans are the allosauroids (large predators such as Allosaurus and Carcharodontosaurus) and the coelurosaurians, which in turn include the tyrannosauroids (such as Tyrannosaurus), the ornithomimosaurs (the ostrich-mimic forms such as Struthiomimus and Ornithomimus) and the maniraptorans. The maniraptorans with their modified wrist and generally large hands are represented by the birds (where the hands became wings) and all their closest relatives, such as the oviraptosaurs (Oviraptor and co), the deinonychosaurs (Velociraptor and co).

Fig 1.- Small coelophysoids lived during the Late Triassic in Great Britain.

Late Triassic Theropods

During the Upper Carnian (~ 220 MYA) of Scotland lived Saltopus elginensis Huene 1910, known from a poorly preserved partial skeleton including dorsal, sacral and caudal vertebrae and fragments of fore and hind limbs (BMNH R3915) found in the Lossiemouth Sandstone Formation, near Elgin, Morayshire. The exact affinities of the animal have been debated. It was either a primitive theropod or a more ancestral dinosauriform.

Theropods were definitely present during the Late Triassic period in the British Isles as proven by the discovery of fragments in the fissure fills of southern Wales. A pelvis, femur and dorsal vertebrae (BMNH PV RU P77/1 and RUP 76/1) from Pant-y-ffynon, Wales of Norian age (~210 MYA), were possibly from a coelophysoid.

The dubious ‘Zanclodon’ cambrensis Newton, 1899 of Rhaetian age (~200 MYA) is known from the mold of a large left dentary with teeth (BGS 6532/BMNH R2912) from Glamorganshire, Wales (Lilstock Fm). This one might be another coelophysoid.

Fig 2.- Larger coelophysoid such as Sarcosaurus roamed the Early Jurassic of England.

Early Jurassic Theropods

In the early Jurassic, coelophysoids are represented by the shadowy Sarcosaurus. The type species, Sarcosaurus woodi Andrews, 1921 is known from a partial pelvis, femur and vertebra (BMNH 4840/1) from Leicestershire (Lias Fm) of Early Sinemurian age (which probably is actually of earlier Late Rhaetian or Hettangian age, ~198-200 MYA). A second species, Sarcosaurus andrewsi Huene, 1932 (= Magnosaurus woodwardi) is based on a partial right tibia (BMNH R3542), originally reported by Woodward in 1908 from Warwickshire of Hettangian age (~198 MYA). Sarcosaurus was a quite large coelophysoid with an estimated length of about 3.5 m.

From the Sinemurian (~192 MYA) Upper Broadford Beds Formation of the Isle of Skye (Scotland) came an incomplete right tibia (NMS.G.1994.10.1), interpreted as belonging to a small theropod, probably another coelophysoid (Benton et al., 1995).

A partial hindlimb from Charmouth, Dorset  (BMNH 39496) that was described by Owen (1861) alongside remains of the ornithischian Scelidosaurus harrisonii was reported from the Lower Lias (Hettangian-Sinemurian). This one was found to be comparable to a megalosaur and would therefore be an early member of this group of large theropods that will dominate the Middle Jurassic period.

Finally, a tooth (BMNH 41352) from the Lias group of Lyme Regis, named ‘Megalosaurus’ lydekkeri von Huene, 1926 (= Magnosaurus lydekkeri), is from an indeterminate theropod.

Original artworks on Paleoexhibit are copyrighted to Nobu Tamura. Do not use without permission (Email: nobu dot tamura at yahoo dot com)


References:

C. W. Andrews. 1921. On some remains of a theropodous dinosaur from the Lower Lias of Barrow-on-Soar. Annals and Magazine of Natural History, series 9 8:570-576

M.J. Benton, D.M. Martill & M.A. Taylor, 1995. The first Lower Jurassic dinosaur from Scotland: limb bone of a ceratosaur theropod from Skye. Scottish Journal of Geology, 31, 177–182.

F. v. Huene. 1910. Ein primitiver Dinosaurier aus der mittleren Trias von Elgin [A primitive dinosaur from the Middle Trias of Elgin]. Geologie und Paläontologie Abhandlungen (n.s.) 8(6):317-322.

D. Naish and D. M. Martill. 2007. Dinosaurs of Great Britain and the role of the Geological Society of London in their discovery: basal Dinosauria and Saurischia. Journal of the Geological Society, London 164:493-510.

O. W. M. Rauhut and A. Hungerbühler. 2000. A review of European Triassic theropods. GAIA 15:75-88.

Sauropods of the British Isles Part III

Fig 1.- Rebbachisaurids were present on the Isle of Wight during the Early Cretaceous.

Sauropods from the Early Cretaceous (part II)

The Wessex Formation of the Isle of Wight

The Wessex formation on the Isle of Wight of Barremian age (~ 127 MYA) has a number of sauropod remains, all very fragmentary but enough to point to a high degree of diversity for this group in the British Isles during the Early Cretaceous.

The presence of Diplodocids is scarce if ever they were present at all. A chevron has been described by Alan Charig (1980) as belonging to a diplodocid, but the identification has since then been disputed.  The presence of Rebbachisaurids, on the other hand, is well attested and is represented by isolated bones, including a characteristic scapula [= shoulder blade]  (MIWG 6544), tail vertebra (MIWG 5384) and possibly teeth.  From these scant remains, it appears that the unnamed British representative of this group is most closely related to the Spanish Demandasaurus and the African Nigersaurus (see my previous post about it).

Brachiosaurids were also certainly there and remains are represented by  ‘Pleurocoelus’ valdensis Lydekker, 1889, based on teeth, dorsal and caudal vertebra found near Cuckfield, East Sussex, Hastings beds and on the Isle of Wight. Usually considered to be dubious, Pleurocoelus valdensis is, according to Ruiz-Omeñaca & Canudo (2005), a perfectly valid taxon that was also present in the Iberian Peninsula. Other possible brachiosaurid remains include  ‘Ornithopsis’ eucamerotus Hulke, 1882, based on a set of pelvis bones (BMNH R97), an unnamed taxon evidenced by a single large cervical vertebra (MIWG 7306) that might have belonged to the largest dinosaur of Europe (Naish et al., 2004), and Eucamerotus foxi Blows, 1995, described from a neural arch (BMNH R2522), two dorsals (BMNH R89-90) and another dorsal from a juvenile specimen (BMNH R2524). Oplosaurus armatus Gervais, 1852, is based on a large tooth (BMNH R964) that may belong to a brachiosaurid, but more recent analysis indicated it is more probably from a camarasaurid (Canudo et al., 2002). Chondrosteosaurus gigas Owen, 1876 is known from two neck vertebrae (BMNH 46869 & BMNH 46870) and is probably a basal titanosauriform, although we cannot say if it is a camarasaurid or a brachiosaurid.

Fig 2.- The specialized Titanosaurs were the dominant group of sauropods at the end of the Early Cretaceous.

The most evolved group of sauropods, the titanosaurs, is represented by Iuticosaurus valdensis LeLoeuff et al., 1993, known from 2 tail vertebrae (BMNH R146a & BMNH 151).

Finally, two dubious taxa are indeterminate sauropods: the Isle of Wight ‘Ornithopsis’ hulkei dorsal vertebra (BMNH R28632) was renamed Bothriospondylus elongatus by Owen in 1875 and ‘Ornithopsis’ eucamerotus by Hulke in 1882. Chondrosteosaurus magnus Owen, 1876 is based on a single partial vertebra (BMNH R98).

The Lower and Upper Greensand

The Lower Greensand Group of Aptian age (~120 MYA) delivered a pelvis and associated sacrum (BMNH R12713) from Luccombe Chine, Isle of Wight of a titanosauriform of some sort (Stroh, 1949, Blows, 1995). Also from the Lower Greensand came Dinodocus mackesoni Owen, 1884, based on a humerus (BMNH 14695) from Hythe, Kent. Possibly another indeterminate titanosauriform.

The Upper Greensand formation (Albian-Cenomanian age, ~112 MYA) in southeastern England bears a few sauropod remains, which are the youngest in the British Isles and all belong to titanosaurs. “Titanosaurus” lydekkeri Huene, 1929 (= Iuticosaurus lydekkeri), based on a vertebra (BMNH 32390) found on the Isle of Wight, was synonymized with Macrurosaurus semnus by McIntosh, 1990, but generally considered a nomen dubium.  Macrurosaurus semnus Seeley, 1876 is based on a set of 25 caudal vertebrae (SM B55630) and 15 more various bits found in Cambridgeshire and of Cenomanian age, and is an indeterminate titanosaur.

This concludes our tour of the sauropods of the British Isles.


Original artworks on Paleoexhibit are copyrighted to Nobu Tamura. Do not use without permission (Email: nobu dot tamura at yahoo dot com)


References:


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