Aesopichthys | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Actinopterygii |
Family: | † Aesopichthyidae |
Genus: | † Aesopichthys Poplin & Lund, 2000 [1] |
Species: | †A. erinaceus |
Binomial name | |
†Aesopichthys erinaceus Poplin & Lund, 2000 [2] | |
Aesopichthys ("Aesop fish") is an extinct genus of palaeoniscoid ray-finned fish from North America. Its fossils are currently only known from the Bear Gulch Limestone located in central Montana which dates to the late Mississippian, also known as the Serpukhovian. It was a deep-bodied member of the group, though not to the extent of what is seen in genera like Platysomus . It possessed a short, blunt snout along with partially-webbed fins. There is only a single species in the genus being A. erinaceus.
Aesopichthys is known from a number of specimens with the holotype, CM 48550, being a natural cast and its counterpart found southwest of Becket, Montana. The animal was originally described, along with Proceramala , in 2000 by Cécile Poplin and Richard Lund though in previous papers it was referred under the nickname "Aesopich". The name Aesopichthys derives from Ancient Greek and translates to "Aesop fish" in reference to the hump the fish shares with the Greek fabulist, Aesop. The species name on the other hand, "erinaceus", derives from Ancient Latin and refers to the spikes on the fish's head and shoulder girdle that are reminiscent to those seen in hedgehogs. [3]
Aesopichthys had a short skull with a blunt, high snout; there is only a notch for the anterior naris present in the nasals with there not being one present for the posterior naris. This nasal bone also forms the front half of the orbit, while being in contact with the dermosphenotic, frontal, and third infraorbital. The premaxille do not meet at the midline of the skull, rather being loosely below the antorbitals. The bones that make out the snout are loosely attached due to the presence of a rostral notch along with gaps in multiple places of the snout. These features increased the flexibility of the skull and is similar to what is seen between Aesopichthys' suborbitals and preoperculum. Just like in other deep-bodied fish, its tall preoperculum is upright. The mouth is near the bottom of the head and has its gape reduced due to the fish's mandibular coronoid process that only reaches to the back of the orbit. A single row of small teeth are present on the animal's premaxilla, maxilla, and dentary.
Due to the fact that the skull roof has not been observed in its entirety, it has been suggested that it rose in a similar way to the shape of the body. The supraorbital of the canal enters the parietal by going through the frontal; this bone then goes into the short anterior pit line. This pit line, along with the transverse pit line, is short though the posterior pit line is long and is directed towards the dermopterotic. The infraorbital canal passes through this bone though it does not enter the dermosphenotic, instead entering the later extrascapular, which causes the bone to be anamestic. Backward-facing tubercles are present in multiple areas of the skull roof along with others seen on the first infraorbital and extrascapulars. The braincase of Aesopichthys is short with the postorbital process being much more ossified than the other areas and is overlapped by the third infraorbital. [3]
The pectoral girdle of Aesopichthys lacks specialized postcleithral scales and has a tall, broad ventral limb. It processes two pairs of extrascapulars with a wide lateral one and a thick, rounded medium one. There are backwards projecting spikes on the posterior lamina of the lateral extrascapular. The presupracleithrum is preserved incompletely in specimens though most likely makes contact of the neurocranium.
One of the most notable features of Aesopichthys is the hump that reaches its full height right before the dorsal fin, only for the body to slope back downwards until the base of the caudal fin. The dorsal fin is made up of an average of 51 rays with rays 13-15 being almost the length of the entire fin base. These rays form a deep, downwards curve after the longest rays, only to increase in height once again towards in end of the dorsal fin. At the back of the dorsal fin, the rays radiate from a fine-scaled lobe and decrease in density overall. The top of the caudal fin is made up of a scaled lobe like other palaeoniscoids which is extends past the last fin ray and is erected at between a 27° and 30° angle to the axis of the body, the average number of rays of this fin is 26.8. All rays of the fin are finely segmented with the leading rays of the ventral lobe having fringing fulcra present and are more closely packed than the tapering rays that make up the lower part. In both of the caudal and dorsal fins, these more well-spaced areas are more flexible than the tightly-packed regions. The anal fin of Aesopichthys is triangular in shape and is made up of an average of 18.5 rays with all but the first 2-3 being articulated. Most of the rays behind these are tightly packed with the last 5-6 being more spaced out.
The pectoral fins of Aesopichthys are made up of up to 14 well-spaced rays supported by a fine-scaled lobe. The space between these rays suggests an extensive inter-ray membrane being present. The pelvic fins are located at the mid-abdominal region of the body and is made up of an average of 12.4 long, strong rays with fine fulcra. The total body size of the largest specimen of Aesopichthys 9 cm (3.54 in). [3]
In the original description of the genus, it was suggested to be a palaeoniscimorph due to the presence of features such as a more anteriorly-placed orbit and maxilla with a postorbital plate, though showing much deeper cheeks than other members of the group. Shown below is the phylogenetic tree in the description, showing the relationships between Aesopichthyidae and "Rhadinichthyid group" fish.
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Since the description, Aesopichthys has appeared in the phylogenies of other papers, such as in Ren & Guang-Hui (2021), which place the animal near other genera such as Kalops and Cosmoptychius due to traits such as the presence of jointed radials that support the pectoral fins and the lobe seen in the caudal fin. Shown below is the phylogeny from said paper. [4]
Aesopichthys was most likely adapted to move through complex environments due to the anatomy of its fins, mostly due to the two distinct parts seen in their morphology. The more tightly-packed areas of the dorsal fin would have helped to stabilized the body during turns while the more wide-spaced areas would have allowed the fish maneuver more easily. [3]
Though comparable to rhadinichthyids, the feeding mechanism was much more specialized in many ways. The presence of thick ganoine ridges would have contributed to the strengthening of the notch on the antorbital. Along with this, due to the lack of firm attachment points with other bones, this bone along with the premaxilla were mobile. The extremely deep maxilla had a large amount of shearing area and has ganione ridges, that along with corresponding ridges on the inner surface, suggests the origin the adductor mandibularis musculature may have when to the front of the maxilla rather than the cheek bones. Its sharp teeth would have been able to occlude simultaneously when the mouth closed. When the mouth was closed, it is possible for the notch in the rostrum to have been able to suction in small particles. These features along with a small gape and vertical suspensorium suggest that Aesopichthys had an extremely strong bite that would have closed rapidly. Along with this, the deep maxilla would have potentially allowed for the increase in volume of the buccal cone.
Due to this large amount of specializations, it is most likely that Aesopichthys would have been chasing after invertebrates and larval fish in the near-shore environment the fish has been found in. [5] With the amount specializations the teeth have, it is possible that Aesopichthys would have browsed on organisms such as algae and bryozoans. [3]
The Bear Gulch Limestone as a whole is a near-shore environment positioned between the latitudes of 10° and 12° north of the equator. The area had a seasonal climate that would move between tropical and semi-arid conditions. While the environment has a high amount of vertebrate diversity including Chondrichthyans like Harpagofututor and Falcatus along with the early coelacanth Allenypterus . However, the invertebrate diversity of Bear Gulch is not as well understood with one of the few examples being the strange potential mollusk Typhloesus . [6] Aesopichthys itself was specifically found in sediments associated with a high amounts of sponges and algae. [3]
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
This glossary of ichthyology is a list of definitions of terms and concepts used in ichthyology, the study of fishes.
The Bear Gulch Limestone is a limestone-rich geological lens in central Montana, renowned for the quality of its marine fossils from the late Mississippian subperiod, about 324 million years ago. It is exposed over a number of outcrops northeast of the Big Snowy Mountains, and is often considered a component of the more widespread Heath Formation. The Bear Gulch Limestone reconstructs a diverse, though isolated, marine ecosystem which developed near the end of the Serpukhovian age in the Carboniferous period. It is a lagerstätte, a particular type of rock unit with exceptional fossil preservation of both articulated skeletons and soft tissues. Bear Gulch fossils include a variety of fish, invertebrates, and algae occupying a number of different habitats within a preserved shallow bay.
Stethacanthidae is an extinct family of prehistoric sharks. It is estimated to have existed approximately between 380 and 300 million years ago. Members of this family are noted for their peculiar dorsal fin.
The Palaeonisciformes, commonly known as "palaeoniscoids" are an extinct grouping of primitive ray-finned fish (Actinopterygii), spanning from the Silurian/Devonian to the Cretaceous. They are generally considered paraphyletic, but their exact relationships to living ray-finned fish are uncertain. While some and perhaps most palaeoniscoids likely belong to the stem-group of Actinopteryii, it has been suggested that some may belong to the crown group, with some of these possibly related to Cladistia and/or Chondrostei. Many palaeoniscoids share a conservative body shape and a similar arrangement of skull bones, though paleoniscoids as a whole exhibit considerable diversity in body shape.
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.
Cyranorhis is an extinct genus of marine ray-finned fish that lived during the Serpukhovian age of the Carboniferous period. One species is known, C. bergeraci in the Bear Gulch Limestone what is now Montana, United States. It is named after French novelist Cyrano de Bergerac.
Cycloptychius is an extinct genus of prehistoric freshwater & marine ray-finned fish that existed throughout much of the Carboniferous period in Eurasia, and possibly into the Early Permian in South Africa. It was a member of the Rhadinichthyidae, a family of basal ray-finned fish that was formerly placed in the now-paraphyletic order Palaeonisciformes.
Chirophryne is a monospecific genus of marine ray-finned fish belonging to the family Oneirodidae, the dreamers, a family of deep sea anglerfishes. The only species in the gneus is Chirophryne xenolophus, the longhand dreamer. This species is known from a few locations in the Atlantic and Pacific Oceans.
The plainchin dreamarm is a species of marine ray-finned fish belonging to the family Oneirodidae, the dreamers, a family of deep sea anglerfishes. It is the only species in the monospecific genus Leptacanthichthys. This species occurs in the North Atlantic and North Pacific Oceans at depths down to 2,000 m (6,600 ft).
Discoserra is a prehistoric ray-finned fish from the Mississippian of the Bear Gulch Limestone in Montana. It is a member of the Guildayichthyiformes with a round body and a skull possessing primitive and modern traits. Discoserra is about 60 mm long. In 2006, Discoserra was hypothesized to be a stem neopterygian, although it has alternatively been placed in Cladistia along with other Guildayichthyiformes.
Nemipterus peronii, the notchedfin threadfin bream, notchedfin butterfly breamrosy threadfin bream or Peron's threadfin bream, is a species of marine ray-finned fish belonging to family Nemipteridae, the threadfin breams. This species occurs in the Indo-West Pacific region.
Squalius valentinus, commonly known as the Valencia chub and the Levantine bagra, is a species of freshwater fish in the carp family Cyprinidae. It was first isolated from the Turia River in Valencia, hence its name. It is considered endangered. This species is differentiated from its cogenerates by having eight branched rays in its dorsal fin; eight branched rays in its anal fin; two rows of pharyngeal teeth on both sides possessing 2 and 5 teeth ; a wide caudal peduncle; its number of gill rakers; the number of scales in its lateral line; the number of scale rows above the latter; by possessing three scale rows below it; by having thirty-nine vertebrae ; showing large 4th and 5th infraorbital bones; a maxilla with a very distinct marked anterior process; exhibiting a frontal bone expanded at the middle; a wide neurocranium bone; the lower branch of the pharyngeal bone being robust; a large and narrow urohyal; as well as genetic differences (allozymes).
Squalius malacitanus, commonly known as the Málaga chub, is a species of freshwater fish in the carp family Cyprinidae. It was first isolated from the Guadalmina River in Málaga, hence its name. It is considered a vulnerable species. S. malacitanus differs from its cogenerate species by having 7–8 branched rays in its dorsal fin, 8 branched rays in the anal lateral line; the number of scale rows above its lateral line; possessing 3 scale rows below its lateral line; 38 vertebrae, 21 abdominal, and 17 caudal; large fourth and fifth infraorbital bones; maxilla without a pointed anterior process; the middle of its frontal bone being narrow, as well as its neurocranium bone; the lower branch of its pharyngeal bone is rather long; and the shortness of the inferior lamina of its urohyal bone.
Astyanax microschemos is a species of characid fish from Brazil. It belongs to the A. scabripinnis species complex and differs from other species outside it by having a lower number of branched anal fin rays and its shallow body depth being about 26.9-29.7 vs more than 35% of its standard length (SL). Compared to species of its own complex, it can be distinguished by the combination of its shallow body depth, and smaller interorbital width. The species name comes from the Greek mikroschemos, meaning "low stature", which refers to the shallow body depth of the animal.
Deuterodon pelecus is a species of characid fish from Brazil. It can be distinguished from other species by: its body depth ; its short and pointed snout smaller than the orbital diameter; and a reduced number of branched anal fin rays. D. pelecus also differs from members of its genus by its characteristic color pattern. It possesses a single humeral spot that is constricted to the region above the lateral line; at the same time it shows a conspicuous midlateral body stripe from opercle to the caudal fin base, an autapomorphy of this precise species. Other Deuterodon species have a humeral spot that is vertically or horizontally elongate and have the midlateral stripe becoming faint near that humeral spot. The species name is derived from the Greek pelekus, meaning "axe", referring to the pigmentation shape resulting from the adjoinment of the humeral spot with the midlateral stripe.
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.
Pentanogmius is an extinct genus of sail-finned ray-finned fish that lived during the Late Cretaceous in what is now Europe and the United States. Five species are currently recognized, 2 from Cenomanian to Turonian Europe and 3 better known species from Coniacian to Campanian North America. The American species inhabited large areas of the Western Interior Seaway, with fossil finds indicating a range from Texas and Alabama in the south to Manitoba, Canada, in the north.
Vaillantella euepiptera is a species of freshwater ray-finned fish, a loach, belonging to the family Vaillantellidae, the longfin loaches. This species is found in Southeast Asia.
Pacorichthys is an extinct genus of palaeoniscoid ray-finned fish from Switzerland. It is currently only known from the Meride Limestone, a part of the Monte San Giorgio palaeontological Lagerstatten, located in Canton Ticino. This deposit dates to the Middle Triassic, specifically the Late Ladinian. It was a small, fusiform fish similar to a large amount of other paleonisciformes though it possessed a expanded, fixed maxillary along with its suboperculum being larger than its operculum. Though not fitting with the paleoenvironments seen in the rest of the group, a Redfieldiiform affinity has been suggested for the genus. There is only a single species in the genus being P. sangiorgii.