Rhizodontida Temporal range: | |
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A fossil of Sauripterus taylori | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Sarcopterygii |
Clade: | Tetrapodomorpha |
Class: | † Rhizodontida |
Order: | † Rhizodontiformes Andrews & Westoll, 1970 |
Genera | |
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Rhizodontida is an extinct group of predatory tetrapodomorphs [3] known from many areas of the world from the Givetian through to the Pennsylvanian - the earliest known species is about 377 million years ago (Mya), the latest around 310 Mya. Rhizodonts lived in tropical rivers and freshwater lakes and were the dominant predators of their age. They reached huge sizes - the largest known species, Rhizodus hibberti from Europe and North America, was an estimated 7 m in length, making it the largest freshwater fish known.
The upper jaw had a marginal row of small teeth on the maxilla and premaxilla, medium-sized fangs on the ectopterygoid and dermopalatine bones, and large tusks on the vomers and premaxillae. On the lower jaw were marginal teeth on the dentary, with fangs on the three coronoids and a huge tusk at the symphysial tip of the dentary. Apparently, the left and right mandibles rotated inwards towards each other on biting. This may have been a kinetic mechanism to dig the marginal teeth more deeply into the prey, to help grip slippery or struggling items.
The trunk was elongated, with pelvic, two dorsal and anal fins much reduced and placed posteriorly The anal and second dorsal fins formed a functional part of the tail. The lateral line system was elaborated on the skull and pectoral girdle - in Strepsodus the main trunk lateral line also had several subsidiary lines running parallel to it. This probably helped rhizodonts detect prey in the turbid, swampy environments where they lived.
Rhizodont pelvic fins are known only from external morphology. They are smaller than the pectoral fins and positioned toward the rear of the body. In comparison to the other fins, the pectoral fins were much enlarged. They had a well-developed internal skeleton surrounded by robust, largely unsegmented lepidotrichia; the whole fin was then covered in deeply overlapping scales. This turned the pectoral fin into a broad paddle.
The cladogram presented below is based on a 2021 study by Clement and colleagues: [4]
Rhizodontida | ||||||||||||||||||||||||||||||||||
Judging from their anatomy, rhizodonts had an extremely powerful bite. They probably employed a 'grip and drag' hunting technique, where prey was ambushed, the tusks sunk in to secure it, and then depending on its size, either thrashed on the surface to subdue it, or dragged to where the rhizodont could consume it without being disturbed. Their prey probably included large sharks, lungfish, and other lobe-finned fishes, and even tetrapods, because all tetrapods at this time still had to lay their eggs in water.
A tetrapod is any four-limbed vertebrate animal of the superclass Tetrapoda. Tetrapods include all extant and extinct amphibians and amniotes, with the latter in turn evolving into two major clades, the sauropsids and synapsids. Some tetrapods such as snakes, legless lizards, and caecilians had evolved to become limbless via mutations of the Hox gene, although some do still have a pair of vestigial spurs that are remnants of the hindlimbs.
Sarcopterygii — sometimes considered synonymous with Crossopterygii — is a taxon of the bony fish known as the lobe-finned fish or sarcopterygians, characterised by prominent muscular limb buds (lobes) within the fins, which are supported by articulated appendicular skeletons. This is in contrast to the other clade of bony fish, the Actinopterygii, which have only skin-covered bony spines (lepidotrichia) supporting the fins.
Acanthostega is an extinct genus of stem-tetrapod, among the first vertebrate animals to have recognizable limbs. It appeared in the late Devonian period about 365 million years ago, and was anatomically intermediate between lobe-finned fishes and those that were fully capable of coming onto land.
Eusthenopteron is a genus of prehistoric sarcopterygian fishes known from several species that lived during the Late Devonian period, about 385 million years ago. It has attained an iconic status from its close relationship to tetrapods. Early depictions of animals of this genus show them emerging onto land, but paleontologists now widely agree that eusthenopteron species were strictly aquatic animals.
Panderichthys is a genus of extinct sarcopterygian from the late Devonian period, about 380 Mya. Panderichthys, which was recovered from Frasnian deposits in Latvia, is represented by two species. P. stolbovi is known only from some snout fragments and an incomplete lower jaw. P. rhombolepis is known from several more complete specimens. Although it probably belongs to a sister group of the earliest tetrapods, Panderichthys exhibits a range of features transitional between tristichopterid lobe-fin fishes and early tetrapods. It is named after the German-Baltic paleontologist Christian Heinrich Pander. Possible tetrapod tracks dating back to before the appearance of Panderichthys in the fossil record were reported in 2010, which suggests that Panderichthys is not a direct ancestor of tetrapods, but nonetheless shows the traits that evolved during the fish-tetrapod evolution
Tiktaalik is a monospecific genus of extinct sarcopterygian from the Late Devonian Period, about 375 Mya, having many features akin to those of tetrapods. Tiktaalik is estimated to have had a total length of 1.25–2.75 metres (4.1–9.0 ft) based on various specimens.
The Tetrapodomorpha are a clade of vertebrates consisting of tetrapods and their closest sarcopterygian relatives that are more closely related to living tetrapods than to living lungfish. Advanced forms transitional between fish and the early labyrinthodonts, such as Tiktaalik, have been referred to as "fishapods" by their discoverers, being half-fish, half-tetrapods, in appearance and limb morphology. The Tetrapodomorpha contains the crown group tetrapods and several groups of early stem tetrapods, which includes several groups of related lobe-finned fishes, collectively known as the osteolepiforms. The Tetrapodomorpha minus the crown group Tetrapoda are the stem Tetrapoda, a paraphyletic unit encompassing the fish to tetrapod transition.
Tristichopterids (Tristichopteridae) were a diverse and successful group of fish-like tetrapodomorphs living throughout the Middle and Late Devonian. They first appeared in the Eifelian stage of the Middle Devonian. Within the group sizes ranged from a few tens of centimeters (Tristichopterus) to several meters.
Kenichthys is a genus of sarcopterygian fish from the Devonian period, and a member of the clade Tetrapodomorpha. The only known species of the genus is Kenichthys campbelli, the first remains of which were found in China in 1993. The genus is important to the study of the evolution of tetrapods due to the unique nature of its nostrils, which provide vital evidence regarding the evolutionary transition of fish-like nostrils to the tetrapod choanae.
Rhizodus is an extinct genus of basal, finned tetrapodomorphs. It belonged to Rhizodontida, one of the earliest-diverging tetrapodomorph clades. Two valid species have been described, both of which lived during the Early Carboniferous epoch. The type species R. hibberti is known from the Viséan stage of the United Kingdom, whereas the species R. serpukhovensis is from the Serpukhovian of Russia. Some fossils referred to the genus Rhizodus have also been found in North America.
Onychodus is a genus of prehistoric lobe-finned fish which lived during the Devonian Period. It is one of the best known of the group of onychodontiform fishes. Scattered fossil teeth of Onychodus were first described from Ohio in 1857 by John Strong Newberry. Other species were found in Australia, England, Norway and Germany showing that it had a widespread range.
Eusthenodon is an extinct genus of tristichopterid tetrapodomorphs from the Late Devonian period, ranging between 383 and 359 million years ago. They are well known for being a cosmopolitan genus with remains being recovered from East Greenland, Australia, Central Russia, South Africa, Pennsylvania, and Belgium. Compared to the other closely related genera of the Tristichopteridae clade, Eusthenodon was one of the largest lobe-finned fishes and among the most derived tristichopterids alongside its close relatives Cabonnichthys and Mandageria.
Tristichopterus, with a maximum length of sixty centimetres, is the smallest genus in the family of prehistoric lobe-finned fish, Tristichopteridae that was believed to have originated in the north and dispersed throughout the course of the Upper Devonian into Gondwana. Tristichopterus currently has only one named species, first described by Egerton in 1861. The Tristichopterus node is thought to have originated during the Givetian part of the Devonian. Tristichopterus was thought by Egerton to be unique for its time period as a fish with ossified vertebral centers, breaking the persistent notochord rule of most Devonian fish but this was later reinspected and shown to be only partial ossification by Dr. R. H. Traquair. Tristichopterus alatus closely resembles Eusthenopteron and this sparked some debate after its discovery as to whether it was a separate taxon.
Barameda is a genus of rhizodont lobe-finned fishes which lived during the Tournaisian stage near the start of the Carboniferous period in Australia; fossils of the genus have been reported from the Snowy Plains Formation. The largest member of this genus, Barameda decipiens, reached an estimated length of around 3–4 metres (9.8–13.1 ft), while smallest species, B. mitchelli is estimated to have had a length of about 35 centimetres (14 in).
Elpistostegalia or Panderichthyida is an order of prehistoric lobe-finned fishes which lived during the Middle Devonian to Late Devonian period. They represent the advanced tetrapodomorph stock, the fishes more closely related to tetrapods than the osteolepiform fishes. The earliest elpistostegalians, combining fishlike and tetrapod-like characters, are sometimes called fishapods, a phrase coined for the advanced elpistostegalian Tiktaalik. Through a strict cladistic view, the order includes the terrestrial tetrapods.
Megalichthyidae is an extinct family of tetrapodomorphs which lived from the Middle–Late Devonian to the Early Permian. They are known primarily from freshwater deposits, mostly in the Northern Hemisphere, but one genus (Cladarosymblema) is known from Australia, and the possible megalichthyid Mahalalepis is from Antarctica.
Laccognathus embryi is an extinct species of porolepiform lobe-finned fish recovered from Ellesmere Island, Canada. It existed during the Frasnian age of the Late Devonian epoch.
Tinirau is an extinct genus of sarcopterygian fish from the Middle Devonian of Nevada. Although it spent its entire life in the ocean, Tinirau is a stem tetrapod close to the ancestry of land-living vertebrates in the crown group Tetrapoda. Relative to more well-known stem tetrapods, Tinirau is more closely related to Tetrapoda than is Eusthenopteron, but farther from Tetrapoda than is Panderichthys. The type and only species of Tinirau is T. clackae, named in 2012.
The evolution of fish began about 530 million years ago during the Cambrian explosion. It was during this time that the early chordates developed the skull and the vertebral column, leading to the first craniates and vertebrates. The first fish lineages belong to the Agnatha, or jawless fish. Early examples include Haikouichthys. During the late Cambrian, eel-like jawless fish called the conodonts, and small mostly armoured fish known as ostracoderms, first appeared. Most jawless fish are now extinct; but the extant lampreys may approximate ancient pre-jawed fish. Lampreys belong to the Cyclostomata, which includes the extant hagfish, and this group may have split early on from other agnathans.
Innovations conventionally associated with terrestrially first appeared in aquatic elpistostegalians such as Panderichthys rhombolepis, Elpistostege watsoni, and Tiktaalik roseae. Phylogenetic analyses distribute the features that developed along the tetrapod stem and display a stepwise process of character acquisition, rather than abrupt. The complete transition occurred over a period of 30 million years beginning with the tetrapodomorph diversification in the Middle Devonian.
Classification after Benton, M.J. (2005) Vertebrate Palaeontology, 3rd ed. Oxford: Blackwell Publishing. ISBN 0-632-05637-1. ISBN 978-0-632-05637-8.