Dimetrodon borealis Temporal range: Middle Permian, | |
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Holotype jaw of D. borealis displayed at the Royal Ontario Museum | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Synapsida |
Family: | † Sphenacodontidae |
Genus: | † Dimetrodon |
Species: | †D. borealis |
Binomial name | |
†Dimetrodon borealis Leidy, 1854 | |
Synonyms | |
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Dimetrodon borealis, formerly known [1] as Bathygnathus borealis, is an extinct species of pelycosaur-grade synapsid that lived about 270 million years ago (Ma) in the Early Middle Permian. A partial maxilla or upper jaw bone from Prince Edward Island in Canada is the only known fossil of Bathygnathus. The maxilla was discovered around 1845 during the course of a well excavation in Spring Brook in the New London area and its significance was recognized by geologists John William Dawson and Joseph Leidy. It was originally described by Leidy in 1854 as the lower jaw of a dinosaur, making it the first purported dinosaur to have been found in Canada, and the second to have been found in all of North America (the first was Clepsysaurus from Pennsylvania, now known to be a phytosaur rather than a dinosaur). [2] The bone was later identified as that of a pelycosaur. Although its current classification as a sphenacodontid synapsid was not recognized until after the discovery of its more famous relative Dimetrodon in the 1870s, Bathygnathus is notable for being the first discovered sphenacodontid. [3] A 2015 study by the researchers from the University of Toronto Mississauga, Carleton University and the Royal Ontario Museum reclassified the species into the genus Dimetrodon. [4]
The teeth of Dimetrodon borealis are long, recurved, and distinctively teardrop-shaped, being widest at the middle rather than the base. The teardrop shape of the teeth is an indication that Dimetrodon borealis belongs to the family Sphenacodontidae. The shape of the maxilla indicates that Dimetrodon borealis had a deep skull like those of other advanced sphenacodontids like Dimetrodon. Like most other species of Dimetrodon, Dimetrodon borealis has an enlarged caniniform tooth near the front of the jaw. [5]
The maxilla of Bathygnathus was found around 1845 in a community in the north of Prince Edward Island called French River. The bone was uncovered by a landowner named Donald McLeod in a layer of shale at the bottom of his well. [2] This layer was part of a red sandstone formation that bears similarities to younger Triassic sandstones in the United Kingdom, leading geologists to think that the deposit dated back to the Triassic rather than the Permian. Canadian geologist John William Dawson purchased the fossil and was the first to recognize its significance. Dawson brought it to the attention of American paleontologist Joseph Leidy, who described it to the Philadelphia Academy of Natural Sciences in 1854. Leidy identified the bone as a lower jaw, a mistake that was not corrected until English paleontologist Richard Owen reinterpreted it as an upper jaw in 1876. Leidy erected the new genus and species Bathygnathus borealis, which means "northern deep jaw" in Greek as a reference to the height of the jaw and its discovery in Canada. He identified it as belonging to a dinosaur, although he never called Bathygnathus a dinosaur in the paper (Dawson later described it as "a carnivorous reptile... one of that giant reptile aristocracy which constituted the highest animal type in the middle or secondary period of geologic time"). [6] Leidy compared Bathygnathus with Thecodontosaurus from the Triassic red beds of the United Kingdom, one of the first dinosaurs to have been described scientifically.
Dawson inferred that Bathygnathus was a fast-moving carnivore, reasoning that its deep skull was similar to the short skulls of fast-moving snakes and unlike the long skulls of slow-moving crocodilians. [6] Local naturalist Francis Bain popularized the image of Bathygnathus as a dinosaur in the late 1800s, describing it as a "deep jawed monster" that could attack prey "with a bound of sixteen or eighteen feet... bearing it to the ground with its great weight, while the powerful claws prevented its escape, and the sabre-armed jaws completed the sanguinary work of destruction." [2]
American paleontologist E. C. Case reclassified Bathygnathus as a pelycosaur (a type of "mammal-like reptile") in 1905, noting its similarities with the genus Dimetrodon , a sail-backed synapsid that was discovered in Texas in the 1870s. [2] In their 1940 overview of pelycosaurs, Alfred Romer and Llewellyn Ivor Price suggested that Bathygnathus might be synonymous with Dimetrodon. [7]
Synapsida is one of the two major clades of vertebrate animals in the group Amniota, the other being the Sauropsida. The synapsids were the dominant land animals in the late Paleozoic and early Mesozoic, but the only group that survived into the Cenozoic are mammals. Unlike other amniotes, synapsids have a single temporal fenestra, an opening low in the skull roof behind each eye orbit, leaving a bony arch beneath each; this accounts for their name. The distinctive temporal fenestra developed about 318 million years ago during the Late Carboniferous period, when synapsids and sauropsids diverged, but was subsequently merged with the orbit in early mammals.
Dimetrodon is an extinct genus of non-mammalian synapsid belonging to the family Sphenacodontidae that lived during the Cisuralian age of the Early Permian period, around 295–272 million years ago. With most species measuring 1.7–4.6 m (5.6–15.1 ft) long and weighing 28–250 kg (62–551 lb), the most prominent feature of Dimetrodon is the large neural spine sail on its back formed by elongated spines extending from the vertebrae. It was an obligate quadruped and had a tall, curved skull with large teeth of different sizes set along the jaws. Most fossils have been found in the Southwestern United States, the majority of these coming from a geological deposit called the Red Beds of Texas and Oklahoma. More recently, its fossils have also been found in Germany and over a dozen species have been named since the genus was first erected in 1878.
Pelycosaur is an older term for basal or primitive Late Paleozoic synapsids, excluding the therapsids and their descendants. Previously, the term mammal-like reptile had been used, and pelycosaur was considered an order, but this is now thought to be incorrect, and seen as outdated.
Edaphosaurus is a genus of extinct edaphosaurid synapsids that lived in what is now North America and Europe around 303.4 to 272.5 million years ago, during the Late Carboniferous to Early Permian. American paleontologist Edward Drinker Cope first described Edaphosaurus in 1882, naming it for the "dental pavement" on both the upper and lower jaws, from the Greek edaphos έδαφος and σαῦρος ("lizard").
Sphenacodontidae is an extinct family of sphenacodontoid synapsids. Small to large, advanced, carnivorous, Late Pennsylvanian to middle Permian "pelycosaurs". The most recent one, Dimetrodon angelensis, is from the latest Kungurian or, more likely, early Roadian San Angelo Formation. However, given the notorious incompleteness of the fossil record, a recent study concluded that the Sphenacodontidae may have become extinct as recently as the early Capitanian. Primitive forms were generally small, but during the later part of the early Permian these animals grew progressively larger, to become the top predators of terrestrial environments. Sphenacodontid fossils are so far known only from North America and Europe.
Eupelycosauria is a large clade of animals characterized by the unique shape of their skull, encompassing all mammals and their closest extinct relatives. They first appeared 308 million years ago during the Early Pennsylvanian epoch, with the fossils of Echinerpeton and perhaps an even earlier genus, Protoclepsydrops, representing just one of the many stages in the evolution of mammals, in contrast to their earlier amniote ancestors.
Gorgonopsia is an extinct clade of sabre-toothed therapsids from the Middle to Upper Permian roughly 265 to 252 million years ago. They are characterised by a long and narrow skull, as well as elongated upper and sometimes lower canine teeth and incisors which were likely used as slashing and stabbing weapons. Postcanine teeth are generally reduced or absent. For hunting large prey, they possibly used a bite-and-retreat tactic, ambushing and taking a debilitating bite out of the target, and following it at a safe distance before its injuries exhausted it, whereupon the gorgonopsian would grapple the animal and deliver a killing bite. They would have had an exorbitant gape, possibly in excess of 90°, without having to unhinge the jaw.
Neosaurus is an extinct genus of pelycosaur-grade synapsids from the Late Carboniferous-Early Permian of the Jura region of France. It is known only from a partial maxilla or upper jaw bone and an associated impression of the bone. The teardrop shape of the teeth in the jaw indicate that Neosaurus belongs to the family Sphenacodontidae, which includes the better-known Dimetrodon from the Southwestern United States. The maxilla was first attributed to an early diapsid reptile in 1857, and later a crocodylomorph in 1869, before finally being identified as a sphenacodont synapsid in 1899, a classification that still holds today.
Ctenospondylus is an extinct genus of sphenacodontid synapsid
Sphenacodon is an extinct genus of synapsid that lived from about 300 to about 280 million years ago (Ma) during the Late Carboniferous and Early Permian periods. Like the closely related Dimetrodon, Sphenacodon was a carnivorous member of the Eupelycosauria family Sphenacodontidae. However, Sphenacodon had a low crest along its back, formed from blade-like bones on its vertebrae instead of the tall dorsal sail found in Dimetrodon. Fossils of Sphenacodon are known from New Mexico and the Utah–Arizona border region in North America.
Secodontosaurus is an extinct genus of "pelycosaur" synapsids that lived from between about 285 to 272 million years ago during the Early Permian. Like the well known Dimetrodon, Secodontosaurus is a carnivorous member of the Eupelycosauria family Sphenacodontidae and has a similar tall dorsal sail. However, its skull is long, low, and narrow, with slender jaws that have teeth that are very similar in size and shape—unlike the shorter, deep skull of Dimetrodon, which has large, prominent canine-like teeth in front and smaller slicing teeth further back in its jaws. Its unusual long, narrow jaws suggest that Secodontosaurus may have been specialized for catching fish or for hunting prey that lived or hid in burrows or crevices. Although no complete skeletons are currently known, Secodontosaurus likely ranged from about 2 to 2.7 metres (7–9 ft) in length, weighing up to 110 kilograms (250 lb).
Platyhystrix is an extinct temnospondyl amphibian with a distinctive sail along its back, similar to the unrelated synapsids, Dimetrodon and Edaphosaurus. It lived during the boundary between the latest Carboniferous and earliest Permian periods throughout what is now known as the Four Corners, Texas, and Kansas about 300 million years ago.
Eothyris is a genus of extinct synapsid in the family Eothyrididae from the early Permian. It was a carnivorous insectivorous animal, closely related to Oedaleops. Only the skull of Eothyris, first described in 1937, is known. It had a 6-centimetre-long (2.4-inch) skull, and its total estimated length was 30 centimetres. Eothyris is one of the most primitive synapsids known and is probably very similar to the common ancestor of all synapsids in many respects. The only known specimen of Eothyris was collected from the Artinskian-lower.
Thalattosaurus meaning "sea lizard," from the Attic Greek thalatta (θάλαττα), "sea," and sauros (σαῦρος), "lizard," is an extinct genus of marine reptile in the family Thalattosauroidea. They were aquatic diapsids that are known exclusively from the Triassic period. It was a 2–3 metres (6.6–9.8 ft) long shellfish-eating reptile with paddle-like limbs and a down-turned rostrum occurring in the Lower and Middle Triassic Sulphur Mountain Formation of British Columbia as well as the Upper Triassic Hosselkus Limestone of California. It has gained notoriety as a result of studies on general diapsid phylogeny.
Aerosaurus is an extinct genus within Varanopidae, a family of non-mammalian synapsids. It lived between 252-299 million years ago during the Early Permian in North America. The name comes from Latin aes (aeris) “copper” and Greek sauros “lizard,” for El Cobre Canyon in northern New Mexico, where the type fossil was found and the site of former copper mines. Aerosaurus was a small to medium-bodied carnivorous synapsid characterized by its recurved teeth, triangular lateral temporal fenestra, and extended teeth row. Two species are recognized: A. greenleeorum (1937) and A. wellesi (1981).
Echinerpeton is an extinct genus of synapsid, including the single species Echinerpeton intermedium from the Late Carboniferous of Nova Scotia, Canada. The name means 'spiny lizard' (Greek). Along with its contemporary Archaeothyris, Echinerpeton is the oldest known synapsid, having lived around 308 million years ago. It is known from six small, fragmentary fossils, which were found in an outcrop of the Morien Group near the town of Florence. The most complete specimen preserves articulated vertebrae with high neural spines, indicating that Echinerpeton was a sail-backed synapsid like the better known Dimetrodon, Sphenacodon, and Edaphosaurus. However, the relationship of Echinerpeton to these other forms is unclear, and its phylogenetic placement among basal synapsids remains uncertain.
Macromerion is an extinct genus of non-mammalian synapsids, specifically Pelycosaurs, in the family Sphenacodontidae from Late Carboniferous deposits in the Czech Republic. It was named as a species of Labyrinthodon in 1875 and as its own genus in 1879.
Homodontosaurus is an extinct genus of therocephalian therapsids from the Late Permian of South Africa. The type species Homodontosaurus kitchingi was named by South African paleontologist Robert Broom in 1949. Broom based his description on a small skull found in the Cistecephalus Assemblage Zone near Graaff-Reinet. The skull is very small, at about 55 millimetres (2.2 in) long and 20 millimetres (0.79 in) wide. Homodontosaurus has large eye sockets and an elongated snout. The lower jaw is long, thin, and curved. Numerous small teeth line the upper jaw and are long, pointed, and round in cross-section.
Gorgodon is an extinct genus of basal synapsids. The genus is monotypic, known only from the type species Gorgodon minutus from the Early Permian of the southwestern United States. The only known remains of Gorgodon are two fossils consisting of fragments of the skull. Gorgodon was described and named by paleontologist Everett C. Olson in 1962 from the San Angelo Formation in Knox County, Texas. Based on what is known of Gorgodon—the squamosal, quadrate, and pterygoid bones of the back of the skull, the maxilla and premaxilla bones that make up the front of the skull, and several teeth—Gorgodon had a relatively large temporal fenestra and a pair large, conical caniniform teeth at the front of the jaw. Other distinguishing features of Gorgodon include the fused connection between the quadrate and squamosal bones and a long transverse process of the pterygoid.
Abdalodon is an extinct genus of late Permian cynodonts, known by its only species A. diastematicus.Abdalodon together with the genus Charassognathus, form the clade Charassognathidae. This clade represents the earliest known cynodonts, and is the first known radiation of Permian cynodonts.