Diabolepis Temporal range: | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Sarcopterygii |
Class: | Dipnoi |
Order: | † Diabolepidiformes |
Family: | † Diabolepididae Schultze, 1993 (name only) |
Genus: | † Diabolepis Chang & Yu, 1987 |
Species: | †D. speratus |
Binomial name | |
†Diabolepis speratus | |
Synonyms | |
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Diabolepis is an extinct genus of very primitive marine lungfish which lived during in the Early Devonian period. It contains a single species, D. speratus of Yunnan, China, from the mid-late Lochkovian of the Xitun Formation. [1] [2] It is one of the oldest known lungfish genera. It is the only member of the family Diabolepididae and the order Diabolepidiformes [3] , although neither of these parent taxa have been officially described, despite their names being in scientific usage. [4]
Diabolepis was originally described as Diabolichthys, but this name was found to be preoccupied by a now-outdated genus name given to the manta ray in the 19th century, thus necessitating a new genus name. [5] [6]
It is generally considered the most basal known dipnoan, although some other studies instead find Youngolepis to be more basal. [7] In addition, some studies do not find it to be a lungfish, but rather a more basal dipnotetrapodomorph. [1] [8] [9] However, other studies have continued to recover it as an early lungfish. [3] [7] [10]
A rather small fish, the fossil has risen to prominence as it has four nares like most fish, while modern lungfish have only two, the hindmost pair having moved on to the palate serving as choanae. This proved that the internal nares of lungfish had evolved independently of those in tetrapods. This has made the internal nares a case of parallel evolution rather than a homology between lungfish and tetrapods. [11]
Diabolepis has a prominent snout; the more recurvature the snout, the greater is the proportion of the premaxilla that is included within the mouth cavity. The teeth within the premaxilla are folded with polyplocodont structure. The maxilla was either toothless or absent or there may have been a gap between the premaxilla and the maxilla. There is an intracranial joint or ventral fissure, two external nostrils, and separate ectopterygoids. One or several bones lie lateral to the anterior end of the postparietals. The skull roof has an incipient "B" bone between the postparietals. The rest of the skull roof has a tendency towards fragmentation into small bones. The endocranium is divided. The anterior nostril lies at the mouth margin. There can only be a narrow space between nostril and mouth, and an interrupted canal has been scored for Diabolepis.[ citation needed ]
Lungfish are freshwater vertebrates belonging to the class Dipnoi. Lungfish are best known for retaining ancestral characteristics within the Osteichthyes, including the ability to breathe air, and ancestral structures within Sarcopterygii, including the presence of lobed fins with a well-developed internal skeleton. Lungfish represent the closest living relatives of the tetrapods. The mouths of lungfish typically bear tooth plates, which are used to crush hard shelled organisms.
Sarcopterygii — sometimes considered synonymous with Crossopterygii — is a clade of vertebrate animals which includes a group of bony fish commonly referred to as lobe-finned fish. These vertebrates are characterised by prominent muscular limb buds (lobes) within their 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 supporting the fins.
Rhipidistia, also known as Dipnotetrapodomorpha, is a clade of lobe-finned fishes which includes the tetrapods and lungfishes. Rhipidistia formerly referred to a subgroup of Sarcopterygii consisting of the Porolepiformes and Osteolepiformes, a definition that is now obsolete. However, as cladistic understanding of the vertebrates has improved over the last few decades, a monophyletic Rhipidistia is now understood to include the whole of Tetrapoda and the lungfishes.
The choanae, posterior nasal apertures or internal nostrils are two openings found at the back of the nasal passage between the nasal cavity and the pharynx, in humans and other mammals. They are considered one of the most important synapomorphies of tetrapodomorphs, that allowed the passage from water to land.
Tetrapodomorpha is 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.
Elginia is an extinct genus of pareiasaurid known from the Late Permian of Scotland and China. It was named for the area around Elgin in Scotland, which has yielded many fossils referred to as the Elgin Reptiles.
Ventastega is an extinct genus of stem tetrapod that lived during the Upper Fammenian of the Late Devonian, approximately 372.2 to 358.9 million years ago. Only one species is known that belongs in the genus, Ventastega curonica, which was described in 1996 after fossils were discovered in 1933 and mistakenly associated with a fish called Polyplocodus wenjukovi. ‘Curonica’ in the species name refers to Curonia, the Latin name for Kurzeme, a region in western Latvia. Ventastega curonica was discovered in two localities in Latvia, and was the first stem tetrapod described in Latvia along with being only the 4th Devonian tetrapodomorph known at the time of description. Based on the morphology of both cranial and post-cranial elements discovered, Ventastega is more primitive than other Devonian tetrapodomorphs including Acanthostega and Ichthyostega, and helps further understanding of the fish-tetrapod transition.
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.
Psarolepis is a genus of extinct bony fish which lived around 397 to 418 million years ago. Fossils of Psarolepis have been found mainly in South China and described by paleontologist Xiaobo Yu in 1998. It is not known certainly in which group Psarolepis belongs, but paleontologists agree that it probably is a basal genus and seems to be close to the common ancestor of lobe-finned and ray-finned fishes. In 2001, paleontologist John A. Long compared Psarolepis with onychodontiform fishes and refer to their relationships.
The Xitun Formation is a palaeontological formation which is named after Xitun village in Qujing, a location in South China. This formation includes many remains of fossilized fish and plants of the Early Devonian period. It was originally referred to as the Xitun Member of the Cuifengshan Formation.
Saharastega is an extinct genus of basal temnospondyl which lived during the Late Permian period, around 251 to 260 million years ago. Remains of Saharastega, discovered by paleontologist Christian Sidor at the Moradi Formation in Niger, were described briefly in 2005 and more comprehensively in 2006. The description is based on a skull lacking the lower jaws.
Porolepiformes is an order of prehistoric lobe-finned fish which lived during the Devonian period. They are thought to represent the sister group to lungfish. The group contains two families: Holoptychiidae and Porolepididae.
Elpistostegalia is a clade containing Panderichthys and all more derived tetrapodomorph taxa. The earliest elpistostegalians, combining fishlike and tetrapod-like characters, such as Tiktaalik, are sometimes called fishapods. Although historically Elpistostegalia was considered an order of prehistoric lobe-finned fishes, it was cladistically redefined to include tetrapods.
Burnetia is an extinct genus of biarmosuchian therapsids in the family Burnetiidae, from the Late Permian of South Africa. Burnetia is known so far from a single holotype skull lacking the lower jaws described by South African paleontologist Robert Broom in 1923. Due to erosion and dorsoventral crushing, features of the skull are hard to interpret. Stutural lines are further distorted by the unusual shape of the skull roof, including many bosses and protuberances.
Chirodipterus is an extinct genus of marine lungfish which lived during the Devonian period. Fossils have been found worldwide, including Germany, China, eastern & western Australia, and the United States (Michigan). However, it has been suggested that the genus as currently defined is polyphyletic, in which case only the German type species would belong to the genus.
Stanocephalosaurus is an extinct genus of large-sized temnospondyls living through the early to mid Triassic. The etymology of its name most likely came from its long narrow skull when compared to other temnospondyls. Stanocephalosaurus lived an aquatic lifestyle, with some species even living in salt lakes. There are currently three recognized species and another that needs further material to establish its legitimacy. The three known species are Stanocephalosaurus pronus from the Middle Triassic in Tanzania, Stanocephalosaurus amenasensis from the Lower Triassic in Algeria, and Stanocephalosaurus birdi, from the middle Triassic in Arizona. Stanocephalosaurus rajareddyi from the Middle Triassic in central India needs further evidence in order to establish its relationship among other Stanocephalosaurs. Like other temnospondyls, Stanocephalosaurus was an aquatic carnivore. Evidence of multiple species discovered in a wide range of localities proves that Stanocephalosaurus were present all across Pangea throughout the early to mid Triassic.
Ossinodus is an extinct genus of stem tetrapod. Fossils have been found from the Ducabrook Formation in Queensland, Australia dating back to the middle Visean stage of the Early Carboniferous (Mississippian). It was originally placed within the family Whatcheeriidae, but the absence of an intertemporal bone as suggested by a recent reconstruction of the skull based on fragmentary material may prove it to be stemward of all whatcheeriids.
The skull roof or the roofing bones of the skull are a set of bones covering the brain, eyes and nostrils in bony fishes and all land-living vertebrates. The bones are derived from dermal bone and are part of the dermatocranium.
Ymeria is an extinct genus of early stem tetrapod from the Devonian of Greenland. Of the two other genera of stem tetrapods from Greenland, Acanthostega and Ichthyostega, Ymeria is most closely related to Ichthyostega, though the single known specimen is smaller, the skull about 10 cm in length. A single interclavicle resembles that of Ichthyostega, an indication Ymeria may have resembled this genus in the post-cranial skeleton.
The evolution of tetrapods began about 400 million years ago in the Devonian Period with the earliest tetrapods evolved from lobe-finned fishes. Tetrapods are categorized as animals in the biological superclass Tetrapoda, which includes all living and extinct amphibians, reptiles, birds, and mammals. While most species today are terrestrial, little evidence supports the idea that any of the earliest tetrapods could move about on land, as their limbs could not have held their midsections off the ground and the known trackways do not indicate they dragged their bellies around. Presumably, the tracks were made by animals walking along the bottoms of shallow bodies of water. The specific aquatic ancestors of the tetrapods, and the process by which land colonization occurred, remain unclear. They are areas of active research and debate among palaeontologists at present.