Umoonasaurus | |
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Holotype specimen nicknamed "Eric" (AM F99374), on display at the Australian Museum | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Reptilia |
Superorder: | † Sauropterygia |
Order: | † Plesiosauria |
Family: | † Leptocleididae |
Genus: | † Umoonasaurus Kear, Schroeder & Lee, 2006 |
Species: | †U. demoscyllus |
Binomial name | |
†Umoonasaurus demoscyllus Kear, Schroeder & Lee, 2006 | |
Umoonasaurus is an extinct genus of plesiosaur belonging to the family Leptocleididae. This genus lived approximately 115 million years ago during the Early Cretaceous period (Aptian-Albian stages), in shallow seas covering parts of what is now Australia. It was a relatively small animal around 2.5 metres (8.2 ft) long. An identifying trait of Umoonasaurus is the presence of three crest-ridges on its skull.
The holotype of Umoonasaurus demoscyllus is AM F99374, an opalized skeleton that has been nicknamed "Eric". It was discovered in the Zorba Extension Opal Field near the town of Coober Pedy, and is very well preserved, representing the most complete opalized fossil of a vertebrate known. Other specimens have also been referred to this species. SAM P2381, discovered in the Andamooka opal fields, is another opalized specimen. SAM 31050 was discovered in the Curdimurka area near Lake Eyre, and SAM P410550, a juvenile specimen, comes from the Neales River region, near the town of Oodnadatta. [1] Another juvenile specimen, SAM P15980, was later referred to this species. All known specimens come from the Bulldog Shale in South Australia, although material very similar to Umoonasaurus has been found in the Darwin Formation in the Northern Territory. [2]
The generic name is a combination of the Antakirinja name for the Coober Pedy region, Umoona, and the Greek word sauros, meaning "lizard." The specific name comes from the Greek words demos and scylla , meaning "of the people" and "sea monster," respectively, referring to the public donations used to acquire the holotype. [1]
Umoonasaurus is a small plesiosaur, a four-flippered marine reptile. The holotype is estimated to have measured 2–2.5 meters (6.6–8.2 ft) long, [3] [2] while the juvenile specimen SAM P15980 was only 70 centimetres (2.3 ft) long at maximum. [2] Umoonasaurus is unusual in possessing a combination of primitive and derived characters. [1]
Umoonasaurus had a small, triangular skull with a length of 22.2 centimeters (8.7 in) and a width of 13 centimeters (5.1 in). A tall, narrow crest is present along the middle of the anterior (front) end of the skull. Two other ridges are present above the orbits (openings for the eyes). The premaxilla bears a dental rosette with five tooth sockets. These would have held long, sharp teeth. Each maxilla bears at least ten tooth sockets. The teeth in positions 4 to 6 would have been very large, while the rest of the teeth would have been smaller and more gracile. The external nares (openings for the nostrils) are very small and positioned close to the orbits. While incompletely preserved, the temporal fenestrae would have likely occupied one third of the length of the skull. The anterior skull roof (composed of the parietals) is lanceolate (shaped like a lance head). The pineal foramen (a depression between the orbits and the temporal fenestrae) is triangular and has raised edges. The vomer (a palatal bone close to the tip of the snout) barely extends posteriorly past the internal nares (opening for the nostrils on the inside of the skull). The region of the pterygoid (another of the palatal bones) that borders the quadrate is squared off. The interpterygoid vacuity (a region enclosed by the left and right pterygoids) is separated into the anterior and posterior interpterygoid vacuities, the former of which is particularly large. The parasphenoid (one of the bones in the braincase) runs over the midline of the narrower posterior interpterygoid vacuity. The surrounding surface of the pterygoid is concave. The basicranium (braincase floor) has gracile paroccipital processes (extensions that connect to other bones in the skull). The basioccipital has robust protuberances and extends behind the pterygoid. [1]
The postcranium of Umoonasaurus is not very specialized, but does have some derived traits. The cervical (neck) centra (vertebral bodies) are taller than wide, and the width of the zygapophyses (projections on the neural arch involved in vertebral articulation) is roughly equal to that of the centrum. The neural spines are laterally (side to side) compressed and blade-like in shape. The ribs are single-headed. The epipodials (the bones that form the forearm and shin) are wider than long. At least five posterior caudal vertebrae are fused into a structure that resembles a pygostyle. [1] The function of this structure is unclear, but it may have been involved in the support of a dermal caudal fin. [4]
Prior to their description, the specimens that would later be assigned to Umoonasaurus were thought to represent a new species of Leptocleidus . [5] In 2006, Kear and colleagues found Umoonasaurus to belong to the superfamily Pliosauroidea and be the most basal member of the family Rhomaleosauridae. They found the latter surprising, as Umoonasaurus was also identified as the last surviving member of that family. Leptocleidus was recovered as a more derived rhomaleosaurid, although it was still considered plausible that the two might be close relatives. [1] In 2008, Smith and Dyke found Umoonasaurus to belong to Leptocleididae instead of Rhomaleosauridae, although still within Pliosauroidea. [6] A 2009 study by Druckenmiller and Russel also recovered Umoonasaurus as a pliosauroid, this time as a possible member of Polycotylidae. [7] In 2010, Ketchum and Benson found Umoonasaurus to be a member of Leptocleididae, although they recovered that family as a member of Plesiosauroidea instead of Pliosauroidea. [8] Umoonasaurus was also recovered as a leptocleidid by Druckenmiller and Knutsen in 2012, who found Leptocleididae to belong to Pliosauroidea once again. [9] A 2013 study by Benson and colleagues found Umoonasaurus to be a close relative of Leptocleidus and to belong to Leptocleidia within Plesiosauroidea. [10] In 2015, Parrilla-Bel and Canudo found Umoonasaurus to be a leptocleidid, and in turn finding Leptocleididae to belong to Leptocleidia, which was once again recovered as a member of Plesiosauroidea. [11] Subsequent analyses have recovered a placement for Umoonasaurus similar to the previous two studies. [12] [13] [14]
Topology recovered by Druckenmiller and Russell (2009) [7]
| Topology of Leptocleidia recovered by Parrilla-Bel and Canudo (2015) [11] |
The crests of Umoonasaurus were likely covered by keratin in life, which would have made the crests considerably taller. Since the crests seem too delicate for defense, intraspecific combat, or skull reinforcement, they likely were used for communication. These structures could have been used for both species recognition and courtship displays, and may have been boldly colored in life. [1] Preserved gut contents of the type specimen include 60 gastroliths and 17 isolated vertebrae of an indeterminate teleost fish. This teleost would have an estimated maximum length of between 182 and 296 mm, suggesting Umoonasaurus was a pelagic predator of the middle trophic level, but does not rule out opportunistic predation on benthic prey. [15] [3] This indicates a preference for small prey items, a view reinforced by the lack of hypercarnivorous adaptations in Umoonasaurus. [1]
All known Umoonasaurus come from the Bulldog Shale, a member of the Marree Subgroup located in the Eromanga Basin of South Australia. [1] The sediments of the Bulldog Shale were deposited from the early Aptian to early Albian stages of the Lower Cretaceous, [16] with Umoonasaurus coming from Aptian [2] deposits laid down approximately 115 million years ago. [1] Some horizons of the Bulldog Shale, including those around Coober Pedy, contain rich opal deposits. [16] Fossilized macroinvertebrates and pollen have been used to recover an early Aptian to early Albian age for this formation. [16] The deposits of the Bulldog Shale represent a coastal region of a shallow epicontinental sea. [17] Dark layers of shale rich in organic material with low planktonic diversity are indictive of dysaerobic waters (those with a low amount of dissolved oxygen) near the bottom. [16] This sea would have been located at a latitude of approximately 70° S, within the polar regions. The presence of glendonite, ice-rafted boulders, and coniferous driftwood with dense growth rings indicate a seasonal climate with near-freezing temperatures. [17] The average temperature of this region has been estimated at 12.2 °C (54.0 °F). [16] This suggests that Umoonasaurus was able to tolerate these cold conditions. [1]
The Bulldog Shale has yielded fossils of plants, invertebrates, fish, and reptiles. [17] The macroinvertebrate fauna of this formation includes several molluscs, such as belemnites, gastropods, and bivalves. Fish are represented by chimaeras (such as Edaphodon ) [3] and bony fish (including teleosts [3] and a lungfish). Sharks are conspicuously absent in the Bulldog Shale. [16] Among the reptiles are other plesiosaurs, including the possible aristonectine elasmosaurid Opallionectes , other indeterminate elasmosaurids, [16] the giant pliosaurid Kronosaurus , and polycotylid-like specimens. The ichthyosaur Platypterigius is also known from the Bulldog Shale. [2]
Plesiosauroidea is an extinct clade of carnivorous marine reptiles. They have the snake-like longest neck to body ratio of any reptile. Plesiosauroids are known from the Jurassic and Cretaceous periods. After their discovery, some plesiosauroids were said to have resembled "a snake threaded through the shell of a turtle", although they had no shell.
Pliosauroidea is an extinct clade of plesiosaurs, known from the earliest Jurassic to early Late Cretaceous. They are best known for the subclade Thalassophonea, which contained crocodile-like short-necked forms with large heads and massive toothed jaws, commonly known as pliosaurs. More primitive non-thalassophonean pliosauroids resembled plesiosaurs in possessing relatively long necks and smaller heads. They originally included only members of the family Pliosauridae, of the order Plesiosauria, but several other genera and families are now also included, the number and details of which vary according to the classification used.
Elasmosauridae is an extinct family of plesiosaurs, often called elasmosaurs. They had the longest necks of the plesiosaurs and existed from the Hauterivian to the Maastrichtian stages of the Cretaceous, and represented one of the two groups of plesiosaurs present at the end of the Cretaceous alongside Polycotylidae.
Microcleidus is an extinct genus of sauropterygian reptile belonging to the Plesiosauroidea. The species has 40 neck vertebrae and a short tail of 28 vertebrae. Fossils of the genus have been found in France, the Posidonia Shale in Germany and Luxembourg, and the Alum Shale Formation of England.
Plesiopleurodon is an extinct genus of Mesozoic marine reptiles, belonging to the Sauropterygia, known from the Late Cretaceous of North America. It was named by Kenneth Carpenter based on a complete skull with a mandible, cervical vertebra, and a coracoid. In naming the specimen, Carpenter noted "Of all known pliosauroids, Plesiopleurodon wellesi most closely resembles Liopleurodon ferox from the Oxfordian of Europe, hence the generic reference." It was initially described as a pliosauroid due to it short neck, a common trait of the superfamily. However, later exploration into the relationships of both groups indicate that not all pliosauroids have short necks and not all plesiosauroids have long necks. Later research indicates it is a member of the Polycotylidae, within the clade Occultonectia.
Cryptoclididae is a family of medium-sized plesiosaurs that existed from the Middle Jurassic to the Early Cretaceous. They had long necks, broad and short skulls and densely packed teeth. They fed on small soft-bodied preys such as small fish and crustaceans. The earliest members of the family appeared during the early Bajocian, and they represented the dominant group of long-necked plesiosaurs during the latter half of the Jurassic.
Polycotylidae is a family of plesiosaurs from the Cretaceous, a sister group to Leptocleididae. They are known as false pliosaurs. Polycotylids first appeared during the Albian stage of the Early Cretaceous, before becoming abundant and widespread during the early Late Cretaceous. Several species survived into the final stage of the Cretaceous, the early Maastrichtian around 72 million years ago. The possible latest surviving member Rarosaurus from the late Maastrichtian is more likely a crocodylomorph.
Leptocleidus is an extinct genus of plesiosaur, belonging to the family Leptocleididae. It was a small plesiosaur, measuring only up to 3 m (9.8 ft).
Nichollssaura is an extinct genus of leptocleidid plesiosaur from the Early Cretaceous Boreal Sea of North America. The type species is N. borealis, found in the early Albian age Clearwater Formation near Fort McMurray, Alberta, Canada.
Archaeonectrus is an extinct genus of pliosaur from the Early Jurassic (Sinemurian) of what is now southeastern England. The type species is Archaeonectrusrostratus, first named by Sir Richard Owen in 1865, which was moved to its own genus by N.I. Novozhilov in 1964. It was a relatively small plesiosaur, measuring 3.4–3.67 m (11.2–12.0 ft) long.
Brancasaurus is a genus of plesiosaur which lived in a freshwater lake in the Early Cretaceous of what is now North Rhine-Westphalia, Germany. With a long neck possessing vertebrae bearing distinctively-shaped "shark fin"-shaped neural spines, and a relatively small and pointed head, Brancasaurus is superficially similar to Elasmosaurus, albeit smaller in size at 3.26 metres (10.7 ft) in length as a subadult.
Hauffiosaurus is an extinct genus of Early Jurassic pliosaurid plesiosaur known from Holzmaden of Germany and from Yorkshire of the United Kingdom. It was first named by Frank Robin O’Keefe in 2001 and the type species is Hauffiosaurus zanoni. In 2011, two additional species were assigned to this genus: H. longirostris and H. tomistomimus.
Plesiopterys is an extinct genus of plesiosaur originating from the Posidonienschiefer of Holzmaden, Germany, and lived during the Early Jurassic period. It is thought to be the sister taxon to all other plesiosauroids including the Plesiosaurus, and is placed outside of the Plesiosauroidea group. Plesiopterys wildi is the one known species within the genus, and is 220 centimeters long, or about 7.2 feet, and its body and skull are both relatively small. It possesses a unique combination of both primitive and derived characters, and is currently displayed at the State Museum of Natural History, Germany.
Rhomaleosauridae is a family of plesiosaurs from the Earliest Jurassic to the latest Middle Jurassic of Europe, North America, South America and possibly Asia. Most rhomaleosaurids are known from England, many specifically from lower Blue Lias deposits that date back to the earliest Jurassic, just at the boundary with the Triassic. In fact, to date only two undisputed rhomaleosaurids were named from outside Europe - the closely related Borealonectes russelli and Maresaurus coccai from Canada and Argentina, respectively. These two species are also the only Middle Jurassic representatives of the family. Rhomaleosauridae was formally named by Kuhn in 1961, originally proposed to include Rhomaleosaurus cramptoni and its relatives, which have short necks and large heads relatively to plesiosauroids like Elasmosaurus and Plesiosaurus, but longer necks and smaller heads relatively to advanced pliosaurids like Pliosaurus and Kronosaurus.
Anningasaura is an extinct genus of basal plesiosaur. It is known from a single type species, A. lymense, discovered in Early Jurassic rocks of Lyme Regis in the United Kingdom.
Hastanectes is an extinct genus of a plesiosaurian with possible pliosaurid affinities known from the Early Cretaceous Wadhurst Clay Formation of the United Kingdom. It contains a single species, Hastanectes valdensis, which was originally thought to be a species of Cimoliasaurus.
Vectocleidus is an extinct genus of leptocleidid plesiosaurian known from the Early Cretaceous Vectis Formation of Isle of Wight, in the United Kingdom. It contains a single species, Vectocleidus pastorum.
This timeline of plesiosaur research is a chronologically ordered list of important fossil discoveries, controversies of interpretation, taxonomic revisions, and cultural portrayals of plesiosaurs, an order of marine reptiles that flourished during the Mesozoic Era. The first scientifically documented plesiosaur fossils were discovered during the early 19th century by Mary Anning. Plesiosaurs were actually discovered and described before dinosaurs. They were also among the first animals to be featured in artistic reconstructions of the ancient world, and therefore among the earliest prehistoric creatures to attract the attention of the lay public. Plesiosaurs were originally thought to be a kind of primitive transitional form between marine life and terrestrial reptiles. However, now plesiosaurs are recognized as highly derived marine reptiles descended from terrestrial ancestors.
The Bulldog Shale is a formation of Early Cretaceous age that forms part of the Marree Subgroup of the Rolling Downs Group, located in the Eromanga Basin of South Australia, Queensland and New South Wales.