Asterolepis Temporal range: | |
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Reconstruction of Asterolepis ornata | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | † Placodermi |
Order: | † Antiarchi |
Family: | † Asterolepididae |
Genus: | † Asterolepis Eichwald, 1840 |
Species | |
See text | |
Synonyms | |
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Asterolepis is an extinct genus of antiarch placoderms from the Devonian of North and South America and Europe. [1] They were heavily armored flat-headed benthic detritivores with distinctive jointed limb-like pectoral fins [2] and hollow spine. [3] The armor plate gives the Asterolepis a box-like shape. Its pectoral fins are also armored but the caudal and dorsal fin are not. The first fossils were named by M. Eichwald in 1840 after noticing star-like markings on the fossils.
"Aster-" means star while "-lepis" means scales. [4] Confusion surrounded the first fossils discovered of this genus, as naturalists were unable to ascertain their place among fishes. In 1844, another author named this same genus Chelonichthys. Later very fine specimens were found in the Old Red Sandstone of Russia and Professor Asmus of Dorpat sent them to the British Museum, noticing fossils exhibited star-like markings. That is when the name Chelonichthys was recognized as a synonym for Asterolepis which Eichwald proposed. [3]
Primitive features such as jaw ossifications, a palatoquadrate, and a Meckel's cartilage are present in the Asterolepis that are important features shared between antiarchs and other Gnathostomata . Additionally the Asterolepis has box-like dermal armour covering the head and thorax with highly modified pectoral fins that are enclosed in interlocking dermal plates protecting a cartilaginous endocranium and gill region. Also, the vertebral column and the pectoral girdle are cartilaginous. [3] The Asterolepis does not have an anal fin or pelvic fins. However it does have a caudal and dorsal fin. Both are covered in similar scales. [5]
The Asterolepis has multiple interlocking dermal plates that form its body armour; anterior ventro-lateral (AVL) plate, posterior lateral plate, posterior ventro-lateral (PVL) plate, anterior median dorsal (AMD) plate, two anterior dorsolateral (ADL) plates, two mixilateral plates, and one posterior median dorsal (PMD) plate. The area considered to be the face is also armored with interlocking dermal plates; nuchal plate, paired paranuchal plate, paired postmarginal plate, postpineal plate, premedian plate, paired lateral plate, and semilunar plate. [6] The cheek region of the head shield is formed by three bones: prelateral, opercular/ sub-marginal, and infraprelateral plates where the prelateral and submarginal plates form the lateral region and the infraprelateral plates form the ventral region [5] The paired pectoral fins are also plated with plates of the dorsal central series (CD1-CD4), plates of the medial marginal series (MM1-MM4), and the plates of the lateral marginal series (ML1-ML4). [6]
The postpineal plate is broader than longer. The premedian plate is thickens as you move posterior. The posterior wall of the premedian plate concaves to form the anterior wall of the orbito-nasal cavity and shows prerostral process. [7] The pineal plate is small, trapezoidal, thin bone that covers the most posterior part of the orbito-nasal cavity. It has a rough ornamented surface and a smooth visceral surface that has a round pineal pit. Also, rough postero-ventro-laterally facing processes in the antero-lateral projections of the plate are present. [7]
The medial marginal plate 4 of the pectoral fin displays short spaced spines that go lateral which are absent on the distal part of the plate. The posterior of this plate is narrow unlike the anterior part that is flat and large. [6] The dorsal central plate 1 of the pectoral fin is long and the external dorsal articular area that is anterior to the unornamented area, is finely covered with tiny meshes [6] The distal segment of the pectoral fin armour was shorter than the proximal segment and formed by 13 bones: the third, fourth, and fifth bones of the central dorsal row, central ventral row, middle marginal row, lateral marginal row, and the terminal. These bones were small, elongated, and hexagonal with the external surface usually ridged. The proximal region of the pectoral fins had articular surfaces covered with narrow grooves. [5]
The surface ornamentation on the nuchal plate is tuberculated and on the AVL plate, the ornamentation is tuberculated as there are tubercles that are arranged in parallel rows. On the postpineal plate some tubercles fuse to form small ridges and some of these radiate from the center of the plate. [6] The middle pit-line groove is well marked and connected to the supratemporal pit-line groove, in turn linked to an external openings for the endolymphatic duct. [7] Asterolepis is part of the family Asterolepididae which was characterized by tuberculated surface sculpturing. The organization of the small tubercles were in random arrangement, arranged in radial rows that were sometimes positioned on low crests, or was absent from the majority of the bones. This was only seen in Asterolepis syasiensis where surface sculpturing was absent except on the anterior mediodarsal where relatively low tubercles were present at the anterior margin while the rest of the bone surface was smooth. [5]
The internasal wall of the rostral plate connects the ventral, anterior, and dorsal walls in order to divide the nasal sacs which are relatively small. The nasal sacs are bound between the rostral plate and the rhinocapsular section of the cartilaginous endocranium and are placed some distance from the telencephalon and opened antero-dorsally. [7] They are located posterior to the nares which were located in the anterior part of the nasal sacs. [5] The structure of the orbito-nasal cavity in the Asterolepis ornata has been studied, providing a detailed description of the premedian, rostral, and pineal plates, and bones of the sclerotic ring. [7] The orbito-nasal fenestra is positioned in the middle of the head shield, leaning more towards the anterior end and is usually spectacle-shaped. [7] Eyes are enclosed within the sclerotic capsule and the nasal cavities open directly above the head of the fish. [7] The visceral surface of the sclerotic ring is smooth and bears small pores and pits. The sclerotic ring is open wide ventrally and the sclerotic capsule consists of three fine plates, sclerotic bones one through three (anterior, medial, and lateral). [7] At the Lode Quarry, Latvia, two specimens of Asterolepis ornata were found to have a fossa deep in the orbital fenestra that is treated to be the hypophysial foramen. [5]
The Asterolepis is blind [8] and eyes and nostrils are directed antero-latero-dorsally. [7] Water would reach the nasal sacs directly through the nostrils and exit the sacs laterally along the anterior process of the sclerotic ring. The tail is covered ganoid scales like the armour which are modified cosmoid scales consisting of a bony basal layer, a layer of dentine, and an outer layer of ganoine. [3] [9] Since the tail doesn't have a high degree of mineralization in comparison to the scales of the internal skeleton making then less likely to be preserved in the fossil record. The tail is also has a dorsal fin, which is an identifying characteristic of Antiarchs.
The medioventral bone, located at the center of the ventral wall of the armor, is absent form the trunk shield at early developmental stages of the Asterolepis ornata. [5] In juvenile Asterolepis found at the Lode Quarry, Latvia, the caudal region was covered with very small, rounded scales. The central row of the distal segment in the pectoral fins of juvenile Asterlepis ornata are fused together unlike their adult counterparts. [5]
Asterolepis chadwiki remains were found in the lower part of the Upper Devonian continental Kataberg Formation in Sullivan County, New York. These remains were the first record of the Asterolepis in North America. The discovery of A. chadwiki extended the stratigraphic and geographic range of this characteristically Middle Devonian fish by occurring in the middle of the Senecan Series or middle Frasnian. [10] The Asterolepis of Stromness is believed to be the oldest organism discovered in the most ancient geological system of Scotland.
Several species within the genus have been described: Asterolepis concatenata, Asterolepis maximus, Asterolepis ornata, Asterolepis verrucosa, [11] Asterolepis estonica, Asterolepis chadwiki, Asterolepis cornutus, Asterolepis dellei, Asterolepis essica, Asterolepis radiata, and Asterolepis sysasiensis.
Asterolepis has two sister taxa, Microbrachium and Pterichthys . Both sister taxa are also carnivores and Pterichtyhs is similarly blind.[ citation needed ]
Taxa considered to be sisters to Asterolepis are Microbrachium and Pterichthys. [11]
In the Blue Fiord Formation of Canada (Nunavut), A. sp was discovered and dated to be from the Eifelian period. At the Mikhailovskii Mine, Zheleznogorsk, of the Russian Federation, fossils of A. radiata, A. syasiensis, A sp. and A ornata, were dated to be from the Lower Frasnian. They were found in beds of sandstone, and clay strata with no other faunal remains, underlying Middle Jurassic formations. The depositional environment of the sediments from the Mikhailovskii Mine was lagoonal. The lithology comprised a combination of poorly lithified gray/blue claystone and black argillaceous sandstone. In Armagh, United Kingdom, A. verrucosa was discovered in marine limestone and dated to around the Mississippian. [8] Fossils of Asterolepis have also been found in the Cuche Formation, Boyacá, Colombia. [12]
Pterichthyodes is a genus of antiarch placoderm fishes from the Devonian period. Its fossils have been discovered in Scotland. They were one of the first species recognized for what they were, as their fossils are common in the Old Red Sandstone formation studied by geologists in the early 19th century. Due to their extreme divergence from modern-day fish, they were a puzzle unsolved until Charles Darwin brought forward his theories on evolution.
Placoderms are vertebrate animals of the class Placodermi, an extinct group of prehistoric fish known from Paleozoic fossils during the Silurian and the Devonian periods. While their endoskeletons are mainly cartilaginous, their head and thorax were covered by articulated armoured plates, and the rest of the body was scaled or naked depending on the species.
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
Bothriolepis was a widespread, abundant and diverse genus of antiarch placoderms that lived during the Middle to Late Devonian period of the Paleozoic Era. Historically, Bothriolepis resided in an array of paleo-environments spread across every paleocontinent, including near shore marine and freshwater settings. Most species of Bothriolepis were characterized as relatively small, benthic, freshwater detritivores, averaging around 30 centimetres (12 in) in length. However, the largest species, B. rex, had an estimated bodylength of 170 centimetres (67 in). Although expansive with over 60 species found worldwide, comparatively Bothriolepis is not unusually more diverse than most modern bottom dwelling species around today.
This glossary of ichthyology is a list of definitions of terms and concepts used in ichthyology, the study of fishes.
Acanthothoraci is an extinct group of chimaera-like placoderms closely related to the rhenanid placoderms. Superficially, the acanthoracids resembled scaly chimaeras and (relatively) heavily armored ptyctodonts. They were distinguished from chimaeras by their large scales and plates, a pair of large spines that emanate from their chests, tooth-like beak plates, and the typical bone-enhanced placoderm eyeball. They were distinguished from other placoderms by differences in skull anatomy and by patterns on the skull plates and thoracic plates that are unique to this order.
Micromyzon akamai is a species of catfish in the family Aspredinidae.
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.
Phyllolepis is the type genus of Phyllolepida, an extinct taxon of arthrodire placoderm fish from the middle to late Devonian. The species of Phyllolepis, themselves, are restricted to the Famennian-aged freshwater strata of the Late Devonian, around 360 million years ago. Fossils of this genus have been found primarily in Europe and North America. The end of the Devonian saw them disappear in a mass extinction.
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.
Holonema is an extinct genus of relatively large, barrel-shaped arthrodire placoderms that were found in oceans throughout the world from the Mid to Late Devonian, when the last species perished in the Frasnian-Fammian extinction event. Most species of the genus are known from fragments of their armor, but the Gogo Reef species, H. westolli, is known from whole, articulated specimens.
Hupehsuchia is an order of diapsid reptiles closely related to ichthyosaurs. The group was short-lasting, with a temporal range restricted to the late Olenekian age, spanning only a few million years of the Early Triassic. The order gets its name from Hubei Province, China, from which many specimens have been found. They are probable members of the clade Ichthyosauromorpha.
Yunnanolepididae is an extinct family of primitive Antiarch placoderms characterized by having short, broad skull roofs, and by having a feature on the visceral side of the posterior medial dorsal plate, the crista transversalis interna posterior, which is diagnostic of antiarchs, turning forward, and lying in front of the posterior ventral process and pit.
Entelognathus primordialis is an early placoderm from the late Silurian of Qujing, Yunnan, 419 million years ago.
Brachydeirus is a genus of small to moderately large-sized arthrodire placoderms from the Late Devonian of Europe, restricted to the Kellwasserkalk Fauna of Bad Wildungen and Adorf.
Microbrachius is an extinct genus of tiny, advanced antiarch placoderms closely related to the bothriolepids. Specimens range in age from the Lower Devonian Late Emsian Stage to the Middle Devonian Upper Givetian Stage. They are characterized by having large heads with short thoracic armor of an average length of 2–4 cm. There are patterns of small, but noticeable tubercles on the armor, with the arrangement varying from species to species. Specimens of Microbrachius have been found in Scotland, Belarus, Estonia, and China.
Romundina is a small, heavily armored extinct genus of acanthothoracid placoderms which lived in shallow marine environments in the early Devonian (Lochkovian). The name Romundina honors Canadian geologist and paleontologist Dr. Rómundur (Raymond) Thorsteinsson of Calgary, Alberta, Canada. Romundina are believed to have lived on Earth between 400 and 419 million years ago. The closest known relative to Romundina is the acanthothoracid Radotina. The type and only described species is R. stellina.
Scutarx is an extinct genus of Aetosauriformes, most commonly regarded by its species name Scutarx deltatylus. Scutarx lived around 230 million years ago during the Carnian and Norian stage of the Late Triassic. Scutarx are “medium sized” paramedian osteoderms belonging to the clade Aetosauria, a heavily armored and more herbivorous cousin of crocodiles.
Qilinyu is a genus of early placoderm from the late Silurian of China. It contains a single species, Qilinyu rostrata, from the Xiaoxiang fauna of the Kuanti Formation. Along with its contemporary Entelognathus, Qilinyu is an unusual placoderm showing some traits more similar to bony fish, such as dermal jaw bones and lobe-like fins. It can be characterized by adaptations for a benthic lifestyle, with the mouth and nostrils on the underside of the head, similar to the unrelated antiarch placoderms. The shape of the skull has been described as "dolphin-like", with a domed cranium and a short projecting rostrum.