Ampelosaurus

Ampelosaurus (/ˌæmpɪloʊˈsɔːrəs/ AM-pi-loh-SOR-əs; meaning "vine lizard") is a titanosaurian sauropod dinosaur hailing from the Late Cretaceous Period of what is now Europe. Its type species is A. atacis, named by Le Loeuff in 1995. A possible unnamed species has given Ampelosaurus an age reaching to the latest Cretaceous, from about 70 to 66 million years ago.

Like most sauropods, it would have had a long neck and tail but it also carried armor in the form of osteoderms. Over 500 bones have been assigned to Ampelosaurus and all but the braincase (assigned to A. sp.) has been assigned to A. atacis. They are assigned to the same species because all the differences in the limb proportions have been linked to individual variation. A. atacis is known from a few, well-preserved teeth and some cranial material. A right scapula was discovered associated with a coracoid. The blade of the scapula, contrary to most titanosaurs, is triangular. The blade narrows at one end instead of showing an expansion like most other genera. A. atacis is also known from a pubis about 75 centimetres (30 in) long and an ilium. Aside from that, it is known from a partial forelimb, and many femora.

Titanosaurians were a flourishing group of sauropod dinosaurs during Cretaceous times. The Spanish locality from the latest Cretaceous of “Lo Hueco” yielded a relatively well preserved, titanosaurian braincase, which shares a number of unique features with A. atacis from France. However, it appeared to differ from A. atacis in some traits also. The specimen has been provisionally identified as Ampelosaurus sp.; it is most likely a mature titanosaurian since the bones of the braincase have largely fused together.

Ampelosaurus lived alongside many other animals. Over 8500 specimens have been found alongside it, including gastropods, bivalves, crocodiles, other sauropods, plants and invertebrates in the Villalba de la Sierra, Gres de Saint-Chinian, Marnes Rouges Inférieures and Gres de Labarre formations. Recent attention has made Ampelosaurus one of the most well-known dinosaurs known from France.

Ampelosaurus
Temporal range: Late Cretaceous, 70–66 Ma
Ampelosaurus mount 4
Skeleton restoration of Ampelosaurus atacis
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Order: Saurischia
Suborder: Sauropodomorpha
Clade: Sauropoda
Clade: Titanosauria
Clade: Lithostrotia
Clade: Lirainosaurinae
Genus: Ampelosaurus
Le Loeuff, 1995
Type species
Ampelosaurus atacis
Le Loeuff, 1995

Description

AmpelosaurusScale
Size compared to a human

Like most sauropods, Ampelosaurus would have had a long neck and tail, but it also carried armor in the form of osteoderms 25 to 28 centimetres (9.8 to 11.0 in) long. The four osteoderms found have three different morphologies, they are plate, bulb, and spine-shaped. Ampelosaurus is thought to have measured 15 metres (49 ft) to 16 metres (52 ft) in length and about 8000 kg in weight.[1][2] Ampelosaurus atacis is known from many unattached bones and teeth. It is one of the best-known dinosaurs from France.[1] It is considered to be a dwarf sauropod by Coria et al. (2005) because it has a smaller size in comparison with its ancestors.[3]

Skeleton

AmpelosaurusDB
Life restoration, with hypothetical osteoderm covering

Ampelosaurus is one of the most completely known titanosaurian sauropods from Europe. Since 1989, over 500 bones discovered at the Upper Cretaceous Bellevue locality of southern France have been assigned to A. atacis. An abundant amount of well-preserved elements have been uncovered at Bellevue. In the original description, only a tooth and some vertebrae were examined. In 2005, a complete description was made by Le Loueff of all known material, allowing Ampelosaurus to be much better understood. All the material has been assigned to the species, and even though there are some differences in limb proportions, it has all been linked to individual variation.[4]

Ampelosaurus atacis skull
Skull of A. atacis

A. atacis is known from a few, well-preserved teeth and some cranial material, a tooth of which was described in its original description. The teeth differentiate Ampelosaurus from Magyarosaurus and Lirainosaurus, both of which are also from Europe. The teeth are different from the two later genera as Ampelosaurus has teeth that are roughly cylindrical in the top with thin expansions at the bottom. They are 21 millimetres (0.83 in) high and about 6 millimetres (0.24 in) wide. Those expansions give its teeth a slight constriction between the root and the crown. The teeth are also quite different from the peg-like teeth of titanosaurids.[4] The teeth, have a general morphology similar to titanosaurians Antarctosaurus and a braincase from Dongargaon. Another skull was described from southern France, but showed some differences, meaning there could have been at least two different titanosaurians in France during the Late Cretaceous.[4]

The scapula was found attached to a coracoid. In the longer direction, the bone is 72 centimetres (28 in) long. The blade of the scapula, contrary to titanosaurs, is triangular, larger closer to the base. The blade narrows distally instead of showing an expansion. Differing from Magyarosaurus and Saltasaurus, the scapula does not have the dorsal crest at the base of the scapular blade. The shape of the coracoid is quadrangular,[1] and the coracoid has a thickened cranial margin.[4]

Ampelosaurus mount 2
Mounted skeleton cast

Ampelosaurus is also known from a pubis, about 75 centimetres (30 in) long. It has a strong distal expansion, that is similar to a titanosaur from Brazil, and a large foramen. Contrary to the South American titanosaurs, the ilium does not have an expansion on the side. The ischium, known from a shaft, is unexpanded distally and very well developed. It is also very flat.[4] An incomplete radius is also known. It lacks the proximal and distal ends, and possesses a very prominent ridge along it.[4] The largest and best-preserved specimens are both ulnas. The right ulna has a total length of 395 millimetres (15.6 in). The right ulna is small and slender, is missing an olecranon, and has a well-marked ridge. The left ulna is larger, with a length of 725 millimetres (28.5 in).[4] The ulna has a deep radial fossa.[5]

About 27 femora are known from Bellevue, making them the most common bone, most of them more-or-less complete. They are very flat craniocaudally but otherwise, lack any unusual features.[4] In a study of its bone physiology, it was found that the maximum known femur length was 1,100 millimetres (43 in), which is much larger than previously known (802 millimetres (31.6 in)). That means, that the ancestors Ampelosaurus were slightly smaller than itself.[6] 18 humeri are also known,[4] but none of them approach the size of the largest femur. The humeri do not have a free medullary cavity.[6] The humeri are robust, about 63 centimetres (25 in) long, with very expanded distal and proximal ends.[4]

Three different types of osteoderms have been recovered at Bellevue. Two with large spines have been uncovered. At the base of each spine, which is about 12 centimetres (4.7 in) tall, are two large foramina. The internal faces are all concavo-convex and have a ridge opposite the spine. In side view, they have two sections, a low half that progressively thickens, and a spine.[4]

Vertebrae

The holotype specimen of A. atacis is a group of three connected dorsal vertebrae. Cervical vertebrae are uncommon from Bellevue and most of them are poorly preserved.[4] The vertebrae are opisthocoelous, with centra that lengthen toward the rear. Neural spines have been preserved on the vertebrae, and they face toward the rear. Two dorsal vertebrae were preserved with a complete, but very crushed neural arch, a neural spine with a characteristic shape: it is very widened distally and narrows downwards. The vertebrae also have an internal structure that is spongy, with very large cells.[1] The caudal vertebrae are all strongly procoelous and are compressed on the sides. The neural spines of the caudal vertebrae are very narrow and very tall and point toward the rear. The middle caudal vertebrae are more compressed on the sides that the others. Also, the centrum of middle caudal vertebrae is longer proportionally.[1] Two sacral vertebrae were known from Bellevue. They are poorly preserved, and are thought to belong to a juvenile. A complete sacrum was also found in 2002.[4]

Distinguishing anatomical features

Ampelosaurus osteoderm
Osteoderm

This set of characters was identified by Le Loeuff in his description of Ampelosaurus to distinguish it from all other genera: teeth that weakly spatulate; a laterally widening distal extremity of neural spines on the dorsal vertebrae; neural arch of the dorsal vertebrae inclining strongly towards the rear; the lack of a distal expansion on the scapular blade; the presence of a light, ventral crest on top of the scapula; the presence of plate, bulb, and spine shaped osteoderms;[1] and, in 2005, Le Loeuff added that the constriction of the neural spine on the dorsal and cervical vertebrae was also probably a characteristic of Ampelosaurus.[4]

Ampelosaurus sp.

Ampelosaurus braincase
Referred braincase and CT scans

A fossil braincase from Lo Hueco was tentatively assigned to an unnamed species of Ampelosaurus, A. sp., in a 2013 article in the journal PLoS ONE. The braincase was found to share many features with A. atacis, such as a back of the skull that is flat. The braincase, MCCM-HUE-8741, is small in size overall, with a front-to-back length of 100.8 millimetres (3.97 in), and the maximum width of the left half being 64.3 millimetres (2.53 in). Parts of the bottom half of the braincase are missing. Even though section are missing, the specimen does not appear to have been deformed much, as the left and right halves are not very different.[7]

Two frontals are preserved. They are each 57.3 millimetres (2.26 in) long and 64.3 millimetres (2.53 in) wide. The upper surface of each frontal is not smooth. One crest runs along the each frontal, and the together the two crests make up the orbital roof. Both parietals have also been found. The connection between them is marked by a ω-shaped crest. Viewed from the side, the parietal has two extensions. These extensions are not fully preserved, but they would have been on the border of the upper temporal fenestrae in their middle. Each parietal was preserved as 79.6 millimetres (3.13 in) wide. The basioccipital of the specimen from Lo Hueco is unique as it has an occipital condyle that is much wider than tall. The occipital condyle has an irregular surface that was probably caused by the loss of the original cartilaginous covering. The complete braincase was especially low in the skull, and was oriented to the side. The occipital condyle is 28.6 millimetres (1.13 in) wide and 15.8 millimetres (0.62 in) tall.[7] The braincase floor is made by the parabasisphenoid. The prootic is a tall but not long bone. The basisphenoid is mostly on the side of it, along with the laterosphenoid, the parietal, and the otoccipital. The length of the prootic from the front to the back is around 10.6 millimetres (0.42 in).[7]

Neuroanatomy

Ampelosaurus endocast
Endocast of the brain showing the labyrinth

Compared with Giraffititan, the inner ear of A. sp. shows a more basal morphology. That feature is possibly related to a restricted range of possible movements that involve head-turning.[7]

Like in Jainosaurus and most other non-avian archosaurs, the hindbrain and midbrain of A. sp. is relatively poorly preserved in the endocast. In contrast with TMM 40435 and a few other taxa such as cf. Cetiosaurus oxoniensis and Giraffatitan, no characteristic "nub" of the cerebellum can be seen. As in TMM 40435 and many other archosaurs, the back of the brain is especially narrow in A. sp.[7]

The cerebral region of the brain is separated from the rest of the brain by a distinct compression caused in the endocranial cavity. The rearmost part of the cerebral region of the braincase has a top with a small expansion. This is different from Jainosaurus. However, relatively much larger expansions are known in the diplodocoid sauropods Dicraeosaurus and Diplodocus. In MCCM-HUE-8741, the small opening in the skull roof middle is responsible for a swelling on the endocast that is suggestive of a pineal system. It is in the exact position where the pineal gland is expected to have been, between the forebrain and the midbrain.[7]

The semicircular canals are contracted, and they are highly curved. The semicircular system of MCCM-HUE-8741 shows also a basal morphology, because the semicircular canals do not attach to each other.[7]

Discovery and naming

Ampelosaurus long bones
Assortment of bones, Musée des dinosaures, France

Ampelosaurus was originally found near the commune of Campagne-sur-Aude in the Aude département of France. It was recovered in the lower levels of the Marnes Rouges Inférieures Formation, which belong to the early Maastrichtian epoch of the Late Cretaceous Period, ~ 70 million years ago. These sediments represent an ancient floodplain with numerous river channels.[1] French paleontologist Jean Le Loeuff first described and named this dinosaur in 1995. Ampelosaurus is derived from the Greek αμπελος, "the vine" and the Latinised Greek saurus, "reptile". Therefore, Ampelosaurus means "vineyard lizard" after the Blanquette de Limoux vineyard. The vineyard is located on the south side of the region Ampelosaurus was found in. The specific name is based on the Latin ajax, the "Aude river".[1]

The first remains were found in a bonebed discovered in 1989, which produced numerous ribs and vertebrae from the back and tail, as well as many limb bones, but no skull material aside from one tooth. Four osteoderms of different sizes and shapes were also recovered from this bonebed. This material comes from several different individuals. Since 1989, more material has been uncovered in the same region of France, including a relatively complete skeleton with some elements of the skull and lower jaw.[4]

Later, in 2001, the Campagne-sur-Aude site was explored again, this time by Gerard Chauvet, Jean-Luc Le Douarec, Colette Rives and Yvonne Vidoux. After 13 years of searching, they had uncovered a mostly complete skeleton that contained much more material, including bones unknown from the holotype. The material all went to the Musee des Dinosaures, and together took about 10 years to assemble.[8]

The A. sp. was discovered in 2007. It was found in the course of the construction of a high-speed rail track connecting Madrid with Valencia, in a fossil site that many animals were found in, in the Villalba de la Sierra Formation. The site was at a locality named “Lo Hueco,” near the village of Fuentes, Castile-La Mancha, Spain. Over the course of several months, a large-scale emergency excavation by over 60 paleontologists and 100 manual workers allowed thousands of specimens of plants, invertebrates, and vertebrates of late Campanian-early Maastrichtian age to be saved, including A. sp.[7]

Classification

Characteristics of the tail vertebrae and the presence of osteoderms indicate that Ampelosaurus belongs to Lithostrotia, a group of derived titanosaurians which also includes Alamosaurus and Saltasaurus.[9] Many other paleotologists have classified Ampelosaurus as belonging to Titanosauria,[10] Saltasauridae,[5] and Titanosauridae.[1][3][11][12] Ampelosaurus may have an uncertain classification, but it is clearly a titanosaur, with many features found in titanosaurs.[1]

Ampelosaurus dorsal vertebra
Dorsal vertebra, Musée des dinosaures, France
Ampelosaurus hand skeleton2
Reconstructed forearm and hand

Below is a cladogram by Klein et al. in 2012, placing Ampelosaurus as a derived titanosaur:[6]

Titanosauria

Phuwiangosaurus

Andesaurus

Argyrosauridae

Argyrosaurus

Paralititan

Aeolosauridae

Janenschia

Aeolosaurus

Santa Rosa indet.

Antarctosauridae

Isisaurus

Alamosaurus

Opisthocoelicaudia

Antarctosaurus

Argentinosaurus

Aegyptosaurus

Epachthosaurus

Nemegtosauridae

Ampelosaurus

Magyarosaurus

Agustinia

Trigonosaurus

Malawisaurus

Rapetosaurus

Nemegtosaurus

Lirainosaurus

Saltasauridae

Rocasaurus

Jabalpur indet.

Malagasy taxon B

Quaesitosaurus

Neuquensaurus

Saltasaurus

Paleobiology

Growth

Ampelosaurus seems to have grown in a way similar to more basal sauropods. After a certain point in its development, the microscopic material of the bone became very different from more basal Sauropoda. Ampelosaurus grew more slowly once the bone microstructure became unique among sauropods. Although Diplodocoidea and basal Macronaria also show an increase in bone growth and a decrease in growth rate around the presumed onset of sexual maturity, it is much more gradual than Ampelosaurus. The process of growing, which in other sauropods started around sexual maturity, was clearly delayed in Ampelosaurus. The period of growth after sexual maturity seems to be shortened in Ampelosaurus and is dominated by slow bone building instead of fast growth.[6] Growth marks are generally rare in sauropods or appearing only late in ontogeny, if at all. The lack of growth marks is suggestive of fast and continuous growth in sauropods, which supports the hypothesis that they achieved large body size through because of fast growth.[6] Ampelosaurus does not show growth marks on any bone sample. This is unusual to be found with the apparently reduced growth rate and high level of bone growth seen in it, as those features are often associated with the occurrence of growth marks.[6]

Histology

Ampelosaurus femur
Fossil femur

EFS, a system found on the surface of bones, is thought to show a growth plateau which indicates that maximum body size and skeletal maturity is reached in an individual. Ampelosaurus has not been known to have EFS, found on most non-titanosaurian sauropods. Magyarosaurus, a closely related titanosaur, Lirainosaurus, a titanosaur related to saltasaurids, Alamosaurus, a saltasaurid, and Phuwiangosaurus, a very basal titanosaur, were also found to have lacked EFS. However, the basal macronarian Europasaurus has been shown to have had EFS, so it was likely just titanosaurians that did not have them. The outer edge of the bones, were EFS would have been found, was well-preserved, and still lacked any fossilized proof of them being present for Ampelosaurus. However, in the PLoS ONE study that found the lack of EFS, the larger specimens were not tested, so Ampelosaurus might have had EFS. This is characteristic of titanosaurs, as diplodocoids and basal macronarians seem to have EFS. A majority of all Ampelosaurus specimens have been found with secondary osteons placed densely in the inner regions of bones, and lightly in outer regions. The osteon orientation found in Ampelosaurus of osteons not only facing across the bone is not typical of Neosauropoda. Also, there is no medullary cavity in any bones of Ampelosaurus. Ampelosaurus seems to have had many ontogenetic stages in its life based on its bone histology.[6]

Paleoecology

Ampelosaurus atacis is known from a specimen from the Marnes Rouges Inférieures Formation. More specifically, it is known from the Bellevue layer, which has produced many vertebrate fossils. Even though it produced many vertebrates, the formation only has a few elements of plants and invertebrates. The vertebrates consist of numerous remains of Ampelosaurus, scales of Lepisosteus, shell fragments of an indeterminate turtle, cranial fragments and teeth of a crocodile, isolated theropod teeth, classified as Dromaeosauridae indet., an indeterminate ankylosaur, and a dentary and many postcranial elements of Rhabdodon priscus.[1][9] The bird Gargantuavis philoinos, and dinosaur eggs have also been recovered.[9]

Another formation A. atacis is known from is Gres de Saint-Chinian. Along with Ampelosaurus, Rhabdodon priscus, Rhabdodon septimanicus, dinosaur eggs, a Nodosauridae indet. (previously known as Rhodanosaurus lugdunensis), "Megalosaurus" pannoniensis, Variraptor mechinorum, an Avialae indet., an Enantiornithes indet., and a possible Abelisauridae indet. are known from this formation.[9]

A. atacis is one of few vertebrates known from the Gres de Labarre Formation. The only other fossils from the formation belong to Rhabdodon priscus and a Nodosauridae indet.[9]

Villalba de la Sierra Formation

LoHueco
Excavation of A. sp. in 2007

The A. sp. is from the latest Cretaceous aged Lo Hueco region in the Villalba de la Sierra Formation. A study shows that the area around Lo Hueco dates to the late Campanian and early Maastrichtian, although a more recent study revised the later date to the latest Maastrichtian.[7] The study showed that Lo Hueco was near the coast of the Tethys Sea,[7] a large seaway through southern Europe and northern Africa. The area directly on the coast was shown to be a brackish-freshwater aquatic environment, with a muddy flood-plain beside it. Lo Hueco was found to be inside the flood-plain. The flood plain was found to have distributary channels of sand and terrigenous material.[13]

About 8500 different marcoremains have been found in Lo Hueco. Sauropods make up the largest amount of the remains with many articulated individuals, caudal vertebrae and teeth. The caudal vertebrae have been identified as being from a titanosaur closely related to Lirainsaurus, but with some differences. The teeth, were assigned to Ampelosaurus atacis. Apart from sauropods, the Villalba de la Sierra Formation has a good representation of carbonized plants, mostly known from branches and leaves, and invertebrates, mostly bivalves and gastropods. Fishes from the formation include lepisosteid, which have plenty of material, and unidentified actinopterygians and teleosteans. Turtle fossils are very common, even more common than fishes. Of all this material, only two different groups have been identified, the bothremydids Polysternon and Rosasia, along with an uncommon undetermined Pancryptodiran. Squamate lizards are known only from a few undetermined specimens, and eusuchian crocodiles are known from a specimen with similarities to Allodaposuchus and Musturzabalsuchus. Ornithischias and theropod dinosaurs are not as common as sauropods but still consist of much material. Basal euornithopods and probable ankylosaurians are known from Lo Hueco. The ankylosaurian remains consist of a few vertebrae. Rhabdodon sp. is known from the formation, and is known from a fair amount of elements. Only two theropods have been identified, both Dromaeosauridae indet., one dromaeosaurine and one velociraptorine.[13]

Biogeography

Dinosaure - La vie en grand - Ampelosaurus atacis - Oeuf - 003
Referred egg

Titanosaurians were a flourishing group of sauropod dinosaurs during Cretaceous times. Fossils of titanosaurians have been found on all continents and their remains are abundant in a number of Late Cretaceous sites. Nonetheless, the cranial anatomy of titanosaurians is still very poorly known.[7] Ampelosaurus is now the best known sauropod from Europe. Others include Magyarosaurus from Hungary and an unnamed species from Catalonia, Spain. Numerous other fragments and isolated bones may or may not belong to any of these forms.[1] While most titanosaurs are found in the southern continents of Gondwana, several derived species are known from Maastrichtian sediments in the Northern Hemisphere, including Alamosaurus in North America and Opisthocoelicaudia in Asia, indicating that there must have been at least intermittent connections between the northern and southern continents. This seems to be corroborated by the European find of Tarascosaurus, a Late Cretaceous theropod dinosaur similar to the abelisaurids, otherwise known only from the southern continents.[14]

Ampelosaurus sp. is a distinct sauropod as it is known from just a braincase. Although the number of sauropod braincases from the Late Cretaceous European archipelago found to date is limited, it shows a significant diversity. The specimen from Lo Hueco resembles the braincase of A. atacis MDE C3–761.[7]

References

  1. ^ a b c d e f g h i j k l Le Loeuff, J. (1995). "Ampelosaurus atacis (nov. gen., nov. sp.), un nouveau Titanosauridae (Dinosauria, Sauropoda) du Crétacé supérieur de la Haute Vallée de l'Aude (France)" (PDF). Comptes Rendus de l'Académie des Sciences. IIa. 321: 693–699.
  2. ^ Paul, G.S., 2010 The Princeton Field Guide to Dinosaurs, Princeton University Press p. 207
  3. ^ a b Salgado, L. & Coria, R.A. (2005). "Sauropods of Patagonia: systematic update and notes on global sauropod evolution". In: Carpenter, K. & Tidwell, V., eds. (2005). Thunder-Lizards: The Sauropodomorph Dinosaurs. Bloomington: Indiana University Press. pp. 430–453. ISBN 978-0-253-34542-4.CS1 maint: Uses editors parameter (link)
  4. ^ a b c d e f g h i j k l m n o Le Loeuff, J. (2005). "Osteology of Ampelosaurus atacis (Titanosauria) from Southern France": In: Tidwell, V. & Carpenter, K., eds. (2005). Thunder-Lizards: The Sauropodomorph Dinosaurs. Bloomington: Indiana University Press. pp. 115–137. ISBN 978-0-253-34542-4.CS1 maint: Uses editors parameter (link)
  5. ^ a b Wilson, J.A. (2002). "Sauropod dinosaur phylogeny: critique and cladistic analysis". Zoological Journal of the Linnean Society. 136 (2): 217–276. doi:10.1046/j.1096-3642.2002.00029.x.
  6. ^ a b c d e f g Klein, N.; Sander, P. M.; Stein, K.; Le Loeuff, J.; Carballido, J. L.; Buffetaut, E. (2012). Farke, Andrew A (ed.). "Modified Laminar Bone in Ampelosaurus atacis and Other Titanosaurs (Sauropoda): Implications for Life History and Physiology". PLoS ONE. 7 (5): e36907. Bibcode:2012PLoSO...736907K. doi:10.1371/journal.pone.0036907. PMC 3353997. PMID 22615842.
  7. ^ a b c d e f g h i j k l Knoll, F.; Ridgely, R. C.; Ortega, F.; Sanz, J. L.; Witmer, L. M. (2013). Butler, Richard J (ed.). "Neurocranial Osteology and Neuroanatomy of a Late Cretaceous Titanosaurian Sauropod from Spain (Ampelosaurus sp.)". PLoS ONE. 8 (1): e54991. Bibcode:2013PLoSO...854991K. doi:10.1371/journal.pone.0054991. PMC 3552955. PMID 23355905.
  8. ^ Souillat, C. & Le Loeuff, J. (2002). "Numéro Spécial 2002". La Lettre de Dinosauria: 1–23.CS1 maint: Uses authors parameter (link)
  9. ^ a b c d e Weishampel, D.B.; Dodson, P. & Osmolska, H. (2004). The Dinosauria (2nd Edition). Berkeley: University of California Press. pp. 259–322, 588–593. ISBN 978-0-520-24209-8.CS1 maint: Uses authors parameter (link)
  10. ^ Wilson, J.A. & Sereno, P.C. (1998). "Early evolution and higher-level phylogeny of sauropod dinosaurs. Society of Vertebrate Paleontology Memoir 5". Journal of Vertebrate Paleontology. 18: 1–68. doi:10.1080/02724634.1998.10011115.CS1 maint: Uses authors parameter (link)
  11. ^ Le Loeuff, J. (1998). "Les dinosaures du Crétacé supérieur de l'Île Ibéro-Armoricaine [The dinosaurs of the Upper Cretaceous of the Ibero-Armorican Island]". In: de Carvalho, A.M.G.; Andrade, A.M.; dos Santos, V.F.; Cascalho, J.; Taborda, R. (eds.). I Encontro Internacional sobre Paleobiologia dos Dinossáurios. Lisboa: Museu Nacional de História Natural. pp. 49–64.CS1 maint: Uses editors parameter (link)
  12. ^ Le Loeuff, J. & Buffetaut, E. (1996). "Ampelosaurus atacis, the dinosaur of the wineyard". The Dinosaur Society UK Quarterly. 1 (4): 1–2.CS1 maint: Uses authors parameter (link)
  13. ^ a b Barroso-Barcenilla, F.; Cambra-Moo, O.; Escaso, F.; Ortega, F.; Pascual, A.; Pérez-García, A.; Rodríguez-Lázaro, J.; Sanz, J. L.; Segura, M.; Torices, A. (2009). "New and exceptional discovery in the Upper Cretaceous of the Iberian Peninsula: The palaeontological site of "Lo Hueco", Cuenca, Spain". Cretaceous Research. 30 (5): 1268. doi:10.1016/j.cretres.2009.07.010.
  14. ^ Le Loeuff, J. & Buffetaut, E. (1991). "Tarascosaurus salluvicus nov. gen., nov. sp., dinosaure théropode du Crétacé supérieur du sud de la France [Tarascosaurus salluvicus, new genus, new species, a theropod dinosaur from the Upper Cretaceous of southern France]". Géobios. 25 (5): 585–594.CS1 maint: Uses authors parameter (link)
Argyrosauridae

Argyrosauridae is a family of large titanosaurian dinosaurs known from the late Cretaceous period of Argentina and Egypt. The group has been recovered as monophyletic, including the type genus Argyrosaurus as well as Paralititan.

Atsinganosaurus

Atsinganosaurus is a genus of titanosaurian dinosaur which existed in what is now France during the late Cretaceous period. Well-preserved remains (and the only known) of Atsinganosaurus were collected from the Grès à Reptiles Formation of the Aix-en-Provence Basin. Atsinganosaurus was first described by Géraldine Garcia, Sauveur Amico, Francois Fournier, Eudes Thouand and Xavier Valentin in 2010, and the type and only species is Atsinganosaurus velauciensis.

The generic name is derived from the Greek word "τσιγγάνος" or "αθίγγανος", both meaning "gypsy", which refers to the possible migration from east to west of the species. The specific name is named after its finding place, Velaux - La Bastide Neuve.A 2018 cladistic analysis of Titanosauria places Ampelosaurus, Atsinganosaurus, and Lirainosaurus in the new lithostrotian clade Lirainosaurinae. New estimates suggest a body size of 8–12 meters, perhaps a max length of 14m for especially large individuals, and a weight of 3 to 5.5 tons.

Austroposeidon

Austroposeidon is an extinct genus of titanosaurian sauropod dinosaur from the Late Cretaceous Presidente Prudente Formation of Brazil. It contains one species, Austroposeidon magnificus.

Brasilotitan

Brasilotitan is a genus of titanosaurian sauropod dinosaur from the Late Cretaceous (early Maastrichtian) Adamantina Formation of Brazil. The type species is Brasilotitan nemophagus.

Dinosauria (museum)

Dinosauria is a museum devoted to dinosaurs in Espéraza, Aude, a département of southern France.

Opened in 1992, it is directed by the association which created it, which is also named Dinosauria. The museum exhibits at least 35 different species of dinosaurs, mounted skeletons or life-size models. It also shows documentary films to the public. The museum collections and rooms include skeletons, paleontological workshops and some other elements. In 2007, the museum received the complete skeleton of an Ampelosaurus atacis specimen, found six years earlier (2001) during excavations in Bellevue (Bèlavista in Occitan), in the town of Campagne-sur-Aude (Campanha d'Aude in Occitan). This skeleton is the most complete dinosaur skeleton of its size ever found in France, and is nicknamed Eva aftere of Eva Morvan, the student who first discovered it during the 2000/2001 excavations.

Diplodocinae

Diplodocinae is an extinct subfamily of diplodocid sauropods that existed from the Late Jurassic to Early Cretaceous of North America, Europe and South America, about 161.2 to 136.4 million years ago. Genera within the subfamily include Tornieria, Supersaurus, Leinkupal, Galeamopus, Diplodocus, Kaatedocus and Barosaurus.Cladogram of the Diplodocidae after Tschopp, Mateus, and Benson (2015).

Epachthosaurus

Epachthosaurus (meaning "heavy lizard") was a genus of dinosaur from the Late Cretaceous. It was a titanosaurid sauropod. Its fossils have been found in Central and Northern Patagonia in South America.

Ferganasaurus

Ferganasaurus was a genus of dinosaur first formally described in 2003 by Alifanov and Averianov. The type species is Ferganasaurus verzilini. It was a sauropod similar to Rhoetosaurus. The fossils were discovered in 1966 in Kyrgyzstan from the Balabansai Formation and date to the Callovian stage of the Middle Jurassic.

Gravisauria

Gravisauria is a clade of sauropod dinosaurs consisting of some genera, Vulcanodontidae and Eusauropoda.

Gres de Labarre Formation

The Gres de Labarre Formation is a geological formation in France whose strata date back to the Late Cretaceous. Dinosaur remains are among the fossils that have been recovered from the formation.

Gres de Saint-Chinian

The Gres de Saint-Chinian is a geological formation in Aude and Hérault, France whose strata date back to the Late Cretaceous. Dinosaur remains are among the fossils that have been recovered from the formation.

Lirainosaurus

Lirainosaurus is a genus of titanosaur sauropod which lived in what is now Spain. The type species, Lirainosaurus astibiae, was described by Sanz, Powell, Le Loeuff, Martinez, and Pereda-Suberbiola in 1999.

Lithostrotia

Lithostrotia is a clade of derived titanosaur sauropods that lived during the Early Cretaceous and Late Cretaceous. The group was defined by Unchurch et al. in 2004 as the most recent common ancestor of Malawisaurus and Saltasaurus and all the descendants of that ancestor. Lithostrotia is derived from the Ancient Greek lithostros, meaning "inlaid with stones", referring to the fact that many known lithostrotians are preserved with osteoderms. However, osteoderms are not a distinguishing feature of the group, as the two noted by Unchurch et al. include caudal vertebrae with strongly concave front faces (procoely), although the farthest vertebrae are not procoelous.

Mansourasaurus

Mansourasaurus ("Mansoura lizard") is a genus of herbivorous lithostrotian sauropod dinosaur from the Quseir Formation of Egypt. The type and only species is Mansourasaurus shahinae.

The discovery of Mansourasaurus was considered quite significant by paleontologists, because very few Late Cretaceous sauropod remains had been found in Africa where the rocky strata that preserve remains elsewhere and produce rich fossil beds were typically not found exposed at or near ground level.

Pilmatueia

Pilmatueia is a diplodocoid sauropod belonging to the family Dicraeosauridae that lived in Argentina during the Early Cretaceous.

Rhabdodon

Rhabdodon (meaning "fluted tooth") is a genus of ornithopod dinosaur that lived in Europe approximately 70–66 million years ago in the Late Cretaceous. It is similar in build to a very robust "hypsilophodont" (non-iguanodont ornithopod), though all modern phylogenetic analyses find this ("Hypsilophodontia/tidae") to be an unnatural grouping, and Rhabdodon to be a basal member of Iguanodontia.

Tambatitanis

Tambatitanis is an extinct genus of titanosauriform dinosaur from the Early Cretaceous (probably early Albian) of Japan. It is known from a single type species, Tambatitanis amicitiae. It was probably around 14 meters long and its mass was estimated at some 4 tonnes. It was a basal titanosauriform and possibly belonged to the Euhelopodidae.

Tengrisaurus

Tengrisaurus (meaning "Tengri lizard") is a genus of lithostrotian sauropod, from the Early Cretaceous (Barremian-Aptian), of the Murtoi Formation, Russia. It was described in 2017 by Averianov & Skutschas. The type species is T. starkovi.

Villalba de la Sierra Formation

The Villalba de la Sierra Formation is a Campanian to Maastrichtian geologic formation in Spain. Fossil dinosaur eggs have been reported from the formation, that comprises gypsiferous, grey, argillaceous mudstones and sandstones, deposited in a floodplain environment. Abundant titanosaurian remains, including Lohuecotitan were found in the formation. More than 10,000 fossil remains of various fishes, amphibians, lizards, dinosaurs (Ampelosaurus sp., Rhabdodon sp.), turtles (Foxemys mechinorum, Iberoccitanemys convenarum), and crocodiles (Lohuecosuchus megadontos, Agaresuchus fontisensis, Musturzabalsuchus sp.) are also known from the site, one of the richest for the Late Cretaceous in Europe.

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