Sphenacodontoids Temporal range: Late Carboniferous-Recent, | |
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Fossilized skull of two sphenacodontoids: Clelandina (Therapsida, Gorgonopsidae) and a Dimetrodon (Sphenacodontidae). | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Synapsida |
Clade: | Sphenacomorpha |
Clade: | Sphenacodontia |
Clade: | Pantherapsida |
Clade: | Sphenacodontoidea Marsh, 1878 |
Clades | |
Sphenacodontoidea is a node-based clade that is defined to include the most recent common ancestor of Sphenacodontidae and Therapsida and its descendants (including mammals). [1] Sphenacodontoids are characterised by a number of synapomorphies concerning proportions of the bones of the skull and the teeth. [2] [3]
The sphenacodontoids evolved from earlier sphenacodonts such as Haptodus and Ianthodon via a number of transitional stages of small, 1-10 kg, faunivore animals. [1] The possible common ancestor of sphenacodontids and therapsids was a carnivorous synapsid that reached moderate or large size and more closely resembled the land-dominant Early Permian sphenacodontids than the small Haptodus. [2] The first predators among Sphenacodontoidea, like Shashajaia , appeared in the tropical western part of Pangea in the Late Carboniferous. [1] Later, in Permian, sphenacodontoids gave rise to the dominant terrestrial carnivores in both sphenacodontid and therapsid groups. [2]
The following taxonomy follows Fröbisch et al. (2011) and Benson (2012) unless otherwise noted. [4] [5]
Class Synapsida
Sphenacodontoidea in a cladogram modified from Huttenlocker et al. (2021): [1]
Synapsida |
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Synapsids are one of the two major clades of vertebrate animals in the group Amniota, the other being the sauropsids, which include reptiles and birds. The synapsids were once the dominant land animals in the late Paleozoic and early Mesozoic, but the only extant group that survived into the Cenozoic are the 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.
A therapsid is a member of the clade Therapsida which is a major group of eupelycosaurian synapsids that includes mammals and their ancestors and relatives. Many of the traits today seen as unique to mammals had their origin within early therapsids, including limbs that were oriented more underneath the body, as opposed to the sprawling posture of many reptiles and salamanders.
Dimetrodon is a genus of non-mammalian synapsid that lived during the Cisuralian age of the Early Permian period, around 295–272 million years ago. It is a member of the family Sphenacodontidae. 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.
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 late Kungurian or 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.
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.
Therocephalia is an extinct clade of eutheriodont therapsids from the Permian and Triassic. The therocephalians ("beast-heads") are named after their large skulls, which, along with the structure of their teeth, suggest that they were carnivores. Like other non-mammalian synapsids, therocephalians were once described as "mammal-like reptiles". Therocephalia is the group most closely related to the cynodonts, which gave rise to the mammals. This relationship takes evidence in a variety of skeletal features.
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.
Haptodus is an extinct genus of basal sphenacodont, 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.
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.
Pantelosaurus is an extinct genus of basal sphenacodonts known from the Early Permian period of Saxony, Germany. It contains a single species, Pantelosaurus saxonicus.
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.
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.
Callibrachion is an extinct genus of caseid synapsids that lived in east-central France during the Lower Permian (Asselian). The holotype and only known specimen (MNHN.F.AUT490) is represented by an almost complete postcranial skeleton associated with skull fragments discovered at the end of the 19th century in the Permian Autun basin in Saône-et-Loire department, in the Bourgogne-Franche-Comté region. It belongs to an immature individual measuring less than 1.50 m in length. Callibrachion was long considered a junior synonym of the genus Haptodus and classified among the sphenacodontid pelycosaurs. In 2015, a new study found that Callibrachion was a different animal from Haptodus and that it was a caseasaur rather than a sphenacodontid. This was confirmed in 2016 by a cladistic analysis which recovered Callibrachion as a basal caseid. Callibrachion's sharp teeth and unenlarged ribcage indicate that this animal was likely faunivorous.
Raranimus is an extinct genus of therapsids of the Middle Permian. It was described in 2009 from a partial skull found in 1998 from the Dashankou locality of the Qingtoushan Formation, outcropping in the Qilian Mountains of Gansu, China. The genus is the most basal known member of the clade Therapsida, to which the later Mammalia belong.
Cutleria is an extinct genus of basal sphenacodontids or derived stem-sphenacodontoid known from the Early Permian period of the Colorado, United States. It contains a single species, Cutleria wilmarthi.
Kenomagnathus is a genus of synapsid belonging to the Sphenacodontia, which lived during the Pennsylvanian subperiod of the Carboniferous in what is now Garnett, Kansas, United States. It contains one species, Kenomagnathus scottae, based on a specimen consisting of the maxilla and lacrimal bones of the skull, which was catalogued as ROM 43608 and originally classified as belonging to "Haptodus" garnettensis. Frederik Spindler named it as a new genus in 2020.
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