| Trichasaurus Temporal range: Kungurian | |
|---|---|
Scientific classification  | |
| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Clade: | Synapsida |
| Clade: | † Caseasauria |
| Family: | † Caseidae |
| Genus: | † Trichasaurus Williston, 1913 |
| Trichasaurus Temporal range: Kungurian | |
|---|---|
| Scientific classification | |
| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Clade: | Synapsida |
| Clade: | † Caseasauria |
| Family: | † Caseidae |
| Genus: | † Trichasaurus Williston, 1913 |
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.
Sauropsida is a clade of amniotes, broadly equivalent to the class Reptilia, though typically used in a broader sense to also include extinct stem-group relatives of modern reptiles and birds. The most popular definition states that Sauropsida is the sibling taxon to Synapsida, the other clade of amniotes which includes mammals as its only modern representatives. Although early synapsids have historically been referred to as "mammal-like reptiles", all synapsids are more closely related to mammals than to any modern reptile. Sauropsids, on the other hand, include all amniotes more closely related to modern reptiles than to mammals. This includes Aves (birds), which are recognized as a subgroup of archosaurian reptiles despite originally being named as a separate class in Linnaean taxonomy.
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mammal-like reptile had been used, and pelycosaur was considered an order, but this is now thought to be incorrect and outdated.
Sphenacodontia is a stem-based clade of derived synapsids. It was defined by Amson and Laurin (2011) as "the largest clade that includes Haptodus baylei, Haptodus garnettensis and Sphenacodon ferox, but not Edaphosaurus pogonias". They first appear during the Late Pennsylvanian epoch. From the end of the Carboniferous to the end of the Permian, most of them remained large, with only some secondarily becoming small in size.
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.
Caseasauria is one of the two main clades of early synapsids, the other being the Eupelycosauria. Caseasaurs are currently known only from the Late Carboniferous and the Permian, and include two superficially different families, the small insectivorous or carnivorous Eothyrididae, and the large, herbivorous Caseidae. These two groups share a number of specialised features associated with the morphology of the snout and external naris.
Varanopidae is an extinct family of amniotes known from the Late Carboniferous to Middle Permian that resembled monitor lizards and may have filled a similar niche. Typically, they are considered to be relatively basal synapsids, although some studies from the late 2010s recovered them being taxonomically closer to diapsid reptiles, recent studies from the early 2020s support their traditional placement as synapsids on the basis of high degree of bone labyrinth ossification, maxillary canal morphology and phylogenetic analyses. A varanopid from the latest Middle Permian Pristerognathus Assemblage Zone is the youngest known varanopid and the last member of the "pelycosaur" group of synapsids.
Ophiacodontidae is an extinct family of early synapsids from the Carboniferous and Permian. Archaeothyris, and Clepsydrops were among the earliest ophiacodontids, appearing in the Late Carboniferous. Ophiacodontids are among the most basal synapsids, an offshoot of the lineage which includes therapsids and their descendants, the mammals. The group became extinct by the Kungurian or the Roadian, replaced by anomodonts, theriodonts, and the diapsid reptiles.
Sphenacodontoidea is a node-based clade that is defined to include the most recent common ancestor of Sphenacodontidae and Therapsida and its descendants. Sphenacodontoids are characterised by a number of synapomorphies concerning proportions of the bones of the skull and the teeth.
Tetraceratops insignis is an extinct synapsid from the Early Permian that was formerly considered the earliest known representative of Therapsida, a group that includes mammals and their close extinct relatives. It is known from a single 90-millimetre-long (3.5 in) skull, discovered in Texas in 1908. According to a 2020 study, it should be classified as a primitive non-therapsid sphenacodont rather than a genuine basal therapsid.
Protoclepsydrops is an extinct genus of early synapsids, found in Joggins, Nova Scotia. The name means 'first Clepsydrops', and refers to it being the predecessor of the other early synapsid Clepsydrops.
Haptodus is an extinct genus of basal sphenacodonts, a member of the clade that includes therapsids and hence, mammals. It was at least 1.5 metres (5 ft) in length. It lived in present-day France during the Early Permian. It was a medium-sized predator, feeding on insects and small vertebrates.
Oedaleops is an extinct genus of caseasaur synapsids from the Early Permian of the Southwestern United States. Fossils have been found in the Cutler Formation in New Mexico, which dates back to the Wolfcampian stage of the Early Permian. All remains belong to the single known species Oedaleops campi. Oedaleops was closely related to Eothyris, and both are part of the family Eothyrididae. Like Eothyris, it was probably an insectivore.
Baldwinonus is an extinct genus of basal synapsids from the Early Permian. The type species is Baldwinonus trux, named in 1940 from the Cutler Formation of New Mexico. A second species, Baldwinonus dunkardensis, was named in 1952 from Ohio. Baldwinonus was first classified in the family Eothyrididae, but the group has since been recognized as a wastebasket taxon for many early synapsids. More recently, Baldwinonus has been placed in the family Ophiacodontidae. Its phylogenetic relationship to other early synapsids remains poorly understood because it is only known from a few fragments of bone.
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.
Milosaurus is an extinct genus of non-mammalian synapsids native to Illinois that was alive during the latest Carboniferous and earliest Permian. It was named in 1970 on the basis of FMNH 701, a partial skeleton, as well as referred material.
Phreatophasma is an extinct genus of synapsids from the Middle Permian of European Russia. It includes only one species, Phreatophasma aenigmatum, which is itself known from a single femur found in a mine near the town of Belebei in Bashkortostan. Phreatophasma comes from a fossil assemblage that is latest Ufimian to earliest Kazanian in age under the Russian stratigraphic scheme, correlating with the Roadian Age under the international stratigraphic timescale. Because the species is based on a single specimen with few diagnostic anatomical features, uncertainty remains as to where it belongs in tetrapod phylogeny; originally interpreted in 1954 as an enigmatic "theromorph" synapsid by Soviet paleontologist Ivan Yefremov, Phreatophasma was later described as a therapsid incertae sedis by American paleontologist Alfred Romer in 1956 and then as a member of a basal synapsid family called Caseidae starting with Everett C. Olson in 1962. Olson's classification was later supported by Canadian paleontologist Robert Reisz in 1986 and American paleontologist Robert L. Carroll in 1988. Ivakhneneko et al. (1997) and Maddin et al. (2008) both considered Phreatophasma an indeterminate synapsid.
Ianthodon is an extinct genus of basal haptodontiform synapsids from the Late Carboniferous about 304 million years ago. The taxon was discovered and named by Kissel & Reisz in 2004. The only species in the taxon, Ianthodon schultzei, was found by separating it from a block that also contained the remains of Petrolacosaurus and Haptodus. The evolutionary significance of the taxon wasn't realized until a publication in 2015. The fossil of this organism was discovered in Garnett, Kansas.
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.
Shashajaia is a genus of extinct non-mammalian synapsids from the late Carboniferous to Early Permian. It was one of the earliest members of the group, coming from the Gzhelian stage. It lived in what is now the Halgaito Formation within the larger Cutler group located in the U.S state of Utah. According to a description study, this synapsid is known from well preserved dentary and jaw fragments. Shashajaia shares many similarities to other sphenacodontids including, enlarged (canine-like) anterior dentary teeth, a dorsoventrally deep symphysis and low-crowned, subthecodont postcanines having festooned plicidentine. The study also found that this genus is close to the evolutionary divergence of the Sphenacodontids and the Therapsids, from which mammalian synapsids arose from. Based on studies done on its teeth, Paleontologists found that as their prey became more terrestrial, synapsids like Shashajaia adapted to life on land and grew larger teeth to deal with larger herbivores in an evolutionary arms race.
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