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80-418: Pterygotus is a genus of giant predatory eurypterid , a group of extinct aquatic arthropods . Fossils of Pterygotus have been discovered in deposits ranging in age from Middle Silurian to Late Devonian , and have been referred to several different species. Fossils have been recovered from four continents; Australia , Europe, North America and South America, which indicates that Pterygotus might have had

160-460: A nomen vanum ("baseless name") as the species is impossible to define. The fossil material with which it was described is undiagnostic and insufficient to establish any meaningful characteristics and as such many fragmentary pterygotid fossils have been referred to it throughout its long history, rendering it effectively synonymous with the family Pterygotidae. More often than not, these fragments consist of patches of pterygotid integument preserving

240-558: A North American species, P. cobbi , from the Pridoli of the United States and Canada. P. arcuatus was originally described from a syntypic series (a series of specimens out of which a particular holotype is not designated) of fossil remains by John William Salter, containing five separate fossil specimens. In 1961, 102 years after its description, Erik N. Kjellesvig-Waering noted that only one of these specimens (Number 89587 of

320-465: A eurypterid, as confirmed by further findings. Dawson reclassified it as a eurypterid in 1871. Kjellesvig-Waering in 1964 assigned it as a questionable species of Pterygotus . In 1921, Ruedemann described an eurypterid fauna from the Vernon Formation of Pittsford , New York. Among them, the species P. vernonensis was erected based on two small short carapaces. The outline and position of

400-476: A highly taxonomically diverse genus. P. barrandei was named in 1898 and has fossil representation in Pridoli age deposits of the Czech Republic . P. barrandei is noted to be very similar to P. cobbi , and a close relation between the two species is assumed. Despite many similarities, the two species do have some differences, most prominently in the cheliceral teeth of the free rami. The largest tooth of

480-492: A kind of "double tooth combination" that is also present in some other species, such as P. lightbodyi , P. impacatus and Erettopterus brodiei . The total length of the fossilized ramus is 2.35 cm (1 in), but it likely only represents around half of the full ramus. As in other species (and the Pterygotidae in general), the teeth are finely ribbed. It can be distinguished from all other species of Pterygotus by

560-604: A large chelicera (specimen number 53890 in the British Museum of Natural History ) originally doubtfully referred to Erettopterus bilobus , P. lanarkensis more closely resembles P. anglicus than it does species of Erettopterus . The terminal tooth (broken in this specimen) is 0.9 cm in length and the central tooth is unusually short. The combination of an unusually long terminal tooth and an underdeveloped central tooth differentiates P. lanarkensis from other species of Pterygotus . Several features distinguish it from

640-451: A nearly cosmopolitan (worldwide) distribution. The type species, P. anglicus , was described by Swiss naturalist Louis Agassiz in 1839, who gave it the name Pterygotus , meaning "winged one". Agassiz mistakenly believed the remains were of a giant fish; he would only realize the mistake five years later in 1844. Pterygotus was among the largest eurypterids. Isolated fossil remains of a large chelicera (frontal appendage) suggests that

720-489: A taxon containing multiple species must be divided into more than one genus, the type species automatically assigns the name of the original taxon to one of the resulting new taxa, the one that includes the type species. The term "type species" is regulated in zoological nomenclature by article 42.3 of the International Code of Zoological Nomenclature , which defines a type species as the name-bearing type of

800-560: A telson (which is far more similar to Erettopterus than to Pterygotus ). Most of these specimens have been lost since the 1870s, the last record being that they were all in the cabinet of a Dr. McCullough of Abergavenny. The 20th century would see the description of additional species of Pterygotus in North America as well, including the Silurian P. marylandicus (1964, Maryland , USA) and P. monroensis (1902, New York, USA),

880-404: A telson, has unusual and pronounced ridges that are not seen in any known species of Pterygotus , nor in any other genus of pterygotid eurypterids, which makes its assignment to Pterygotus questionable. In 1964, two species described by Kjellesvig-Waering increased the known range of Pterygotus to Scotland ( P. lanarkensis ) and Estonia ( P. impacatus ), both Ludlow in age. P. lanarkensis

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960-502: Is an incomplete chelicerae, PE5105, that remains housed at the Chicago Natural History Museum alongside the paratype specimens. The species can be differentiated from other species of Pterygotus primarily by features of its cheliceral teeth, differing from P. barrandei and P. cobbi in these teeth being less-developed and thicker in P. carmani as well as the teeth having a markedly different arrangement on

1040-742: Is based on the nine best-known pterygotid species and two outgroup taxa ( Slimonia acuminata and Hughmilleria socialis ). The cladogram also contains the maximum sizes reached by the species in question, which have been suggested to possibly have been an evolutionary trait of the group per Cope's rule ("phyletic gigantism"). Hughmilleria socialis (20 cm) Slimonia acuminata (100 cm) Ciurcopterus ventricosus (70 cm) Erettopterus waylandsmithi (60 cm) Erettopterus osiliensis (90 cm) Erettopterus serricaudatus (60 cm) Erettopterus bilobus (70 cm) Pterygotus anglicus (160 cm) Jaekelopterus rhenaniae (250 cm) Eurypterid Too Many Requests If you report this error to

1120-544: Is classified as part of the pterygotid family of eurypterids, to which it lends its name, a group of highly derived eurypterids of the Silurian to Devonian periods that differ from other groups by a number of features, perhaps most prominently in the chelicerae (the first pair of limbs) and the telson (the posteriormost division of the body). The chelicerae of the Pterygotidae were enlarged and robust , clearly adapted to be used for active prey capture and more similar to

1200-418: Is classified within the family Pterygotidae in the superfamily Pterygotioidea , lending its name to both its family and its superfamily. The three most derived pterygotid eurypterids, Acutiramus , Jaekelopterus and Pterygotus , are very similar to each other. Pterygotus is particularly similar to Jaekelopterus , from which it is virtually only distinct in features of the genital appendage and potentially

1280-406: Is effectively a composite composed of fossils of three different eurypterids. These fossils consist of a type specimen of chelicerae (which is now lost, complicating any potential comparisons), a large carapace and chelicerae (likely actually referrable to Pterygotus due to being similar to P. anglicus ), a leg (undoubtedly representing a carcinosomatid eurypterid, potentially Carcinosoma ) and

1360-562: Is known from a single specimen (No. 48393 of the British Museum of Natural History) includes about half of the anterior end of what is presumed to be a fixed ramus of a chelicera. The claw is stout, with unusually short teeth that are faintly ribbed. This partial ramus measures 1.4 cm (0.5 in) in length and was discovered at Whitcliffe in Shropshire, England associated with fossils of brachiopods and cephalopods. Though it

1440-494: Is seen in the type species of Pterygotus , P. anglicus , and was noted to in fact be more similar to what is seen in P. buffaloensis and P. bohemicus . Today P. buffaloensis is considered a junior synonym of P. bohemicus , which has been reclassified as part of the closely related genus Acutiramus . The fragmentary remains of P. nobilis makes further studies of its precise identity difficult, Semper suggested that it may be synonymous with Acutiramus bohemicus , but noted that

1520-410: Is sometimes considered synonymous with P. lightbodyi , P. denticulatus can be distinguished by the small, thick and curved teeth of its claws, differing not only from P. lightbodyi in this respect, but virtually all other species of Pterygotus as well. P. lightbodyi is named in honor of Robert Lightbody , a British amateur geologist who made valuable contributions to paleontological research on

1600-445: Is sometimes used as a distinguishing feature, though the telsons of the three derived pterygotid genera are all paddle-shaped (the telson of Jaekelopterus is triangular, but might fall into the morphological range of the other genera). An inclusive phylogenetic analysis with multiple species of Acutiramus , Pterygotus and Jaekelopterus is required to resolve whether or not the genera are synonyms of each other. The cladogram below

1680-428: Is theoretically associated with a type species. In practice, however, there is a backlog of untypified names defined in older publications when it was not required to specify a type. A type species is both a concept and a practical system that is used in the classification and nomenclature (naming) of animals. The "type species" represents the reference species and thus "definition" for a particular genus name. Whenever

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1760-401: Is to bear the name). The species name in turn is fixed, in theory, to a type specimen. For example, the type species for the land snail genus Monacha is Helix cartusiana , the name under which the species was first described, known as Monacha cartusiana when placed in the genus Monacha . That genus is currently placed within the family Hygromiidae . The type genus for that family is

1840-465: Is to other pterygotid species discovered in the P. cobbi locality (such as Acutiramus macrophthalmus ). By 1859, 10 species had been assigned to the genus, and John William Salter recognized that it was possible to divide these species into subgenera based on the morphology of the telsons. Salter erected the subgenus Pterygotus ( Erettopterus ) for species with a bilobed telson. Further subgenera would be named as more differences were noted between

1920-423: Is unusually large in this species. The terminal tooth measures 2.3 cm (1 in) in length. The rami of P. impacatus are ornamented with large and pointed pustules (elevations in the skin), and this feature helps distinguish specimens of P. impacatus from other pterygotids in the fossil sites where its remains are found. In 2007, O. Erik Tetlie cast doubt on the assignment of P. impacatus to Pterygotus as

2000-651: The Erettopterus that it was found associated with, including the more robust chelicerae of P. lanarkensis . P. impacatus, recovered from deposits of Ludlow age at Kielkond in Saaremaa , Estonia, is represented by a holotype specimen consisting of a fragmentary free ramus of a chelicera that preserves some diagnostic and well-preserved details (specimen number 7059/7 housed in the Museum of Comparative Zoology ). Alongside this specimen, important specimens referred to

2080-439: The P. carmani remains were found, P. carmani is primarily known from incomplete chelicerae and gnathobases of coxae. Alongside the two coxae and three chelicerae part of its original description, known fossil remains also include a metastoma and a pretelson. All of these original fossil specimens were designated by Kjellesvig-Waering as paratype specimens upon the original description of the species. The designated type specimen

2160-407: The claws of some modern crustaceans , with well developed teeth on the claws, than to the chelicerae of other eurypterid groups. Unlike most of the rest of the body, which was covered in a scale-like ornamentation like other pterygotid eurypterids, the claws lacked any type of ornamentation. Additionally, the end points of the claws were round and curved unlike the sharp points present at the ends of

2240-406: The type species , grew to 1.6 metres (5.2 ft) in length, based on a large tergite discovered by Henry Woodward at some point between 1866 and 1878. Measuring just over 40 centimetres (16 in) in length and 10.5 centimetres (4.1 in) in width, the tergite suggests a eurypterid with a full length of 1.6 metres (5.2 ft) from the beginning of the carapace to the end of the telson, if

2320-478: The "peculiar hook-like termination of the ramus", a feature now known to be present due to a remnant of the free ramus being present in the fossil. The tooth pattern and shape of the claw suggests that an assignment to Pterygotus is more likely. P. siemiradzkii , described by Embrik Strand in 1926 based on fossil material from western Ukraine , is based on highly fragmentary material with little diagnostic value. The single specimen designated as P. siemiradzkii ,

2400-570: The "questions [about its identity] can not be answered from the material available to me". Another species, P. kopaninensis , also named in 1872, is known from a single and incomplete fixed cheliceral ramus (specimen number L1396) recovered from the Kopanina Formation around the village of Zadní Kopanina , located in Prague . The specimen measures 4.3 cm (1.7 in) in length and was at one point assigned to Erettopterus due to

2480-587: The 20th century would help establish that Pterygotus as a genus achieved a nearly cosmopolitan distribution . The first eurypterid to be discovered in Australia was Pterygotus australis , whose fossils were found in the Ludlow age Melbourne Group of the Dargile Formation . The fossils referred to P. australis , consisting of four fragments making up about half of a segment that were discovered during

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2560-935: The Early Devonian P. carmani (1961, USA) and P. floridanus (1950, Florida, USA) and the Middle Devonian P. gaspesiensis (1953, Quebec , Canada). Fossil remains of pterygotid eurypterids, bearing the distinct scale-like ornamentation known from the group, had been reported from eastern Canada as early as 1846, when researcher William Edmond Logan reported the occurrence of an animal "bearing strong resemblance to Murchison's Pterygotus problematicus " in Silurian-Devonian deposits of Gaspé, Quebec . The fossils, eventually identified as being exclusively of Devonian age, were first tentatively referred to P. atlanticus (now synonymized with P. anglicus ), which had been discovered in relatively close proximity to

2640-567: The Gaspé fossils, on the account of the P. atlanticus material being so fragmentary that it was impossible to tell whether or not they represented the same species. They were described by Loris S. Russell as belonging to the new species P. gaspesiensis in 1953. John William Dawson in 1861 named a new species of lycopod plant, Selaginites formosus , based on alleged remains of stems and branches found at Gaspé. Salter convinced Dawson that fossils of S. formosus actually were fragmentary remains of

2720-495: The Geological Survey and Museum of London, a free ramus of a chelicera) might truly be referrable to this distinct species as the other fossils (tergites, coxae and indeterminable fragments) might actually represent fossils of other species due to not being diagnostic enough. P. ludensis , described by Salter in 1859, can be distinguished from other species by the more developed and prolonged keel (or ridge) running along

2800-517: The Wikimedia System Administrators, please include the details below. Request from 172.68.168.132 via cp1112 cp1112, Varnish XID 948324388 Upstream caches: cp1112 int Error: 429, Too Many Requests at Thu, 28 Nov 2024 08:47:57 GMT Type species In botanical nomenclature , these terms have no formal standing under the code of nomenclature , but are sometimes borrowed from zoological nomenclature. In botany,

2880-546: The arrangement of the smaller teeth of the claws and from P. barrandei in that P. floridanus has a more slender ramus. P. carmani is the most commonly found eurypterid in the Lower Devonian deposits of Lucas County, Ohio . Described by Erik N. Kjellesvig-Waering in 1961 and named in honor of Dr. J. Ernest Carman of the Ohio State University, the first to discover eurypterids at the locality where

2960-575: The center of the telson from its beginning to the tail spike. The rare species P. cobbi , described by James Hall in 1859 based on fossils recovered in New York, USA, was the first species of Pterygotus to be described from outside of Scotland and expanded the known range of the genus considerably. Hall described this new species alongside two other North American species; P. macrophthalmus (now referred to Acutiramus ) and P. osborni (later synonymized with P. macrophthalmus ). The distal tooth of

3040-625: The claw. P. marylandicus , from deposits of Ludfordian (Late Silurian) age, is known from a fragmentary and small telson from the McKenzie Formation , Maryland first described by Kjellesvig-Waering in 1964, who recognized it as a telson of a Pterygotus . The specimen (No. 140901 at the United States National Museum ) is very wide, 0.75 cm, and has a nearly straight base with the margins converging anteriorly. Unlike some species, there are no serrations on

3120-465: The claws of the related Erettopterus . The pterygotid telsons were flattened and expanded, likely used as rudders when swimming. Their walking legs were small and slender, without spines, and they were likely not capable of walking on land. Pterygotus is distinguishable from other pterygotids by the curved distal margin of the chelae (claws). The prosoma (head) is subtrapezoidal (a trapezoid with rounded corners), with compound eyes located near

3200-584: The continent, with New York State representing the most fossil-rich state. The remains of P. floridanus were first uncovered by G. Arthur Cooper in Suwannee County, Florida , and the fossils consist of a fixed ramus of the chelicera as well as fragments of the abdominal plates and tergites and were concluded to represent a new species of Pterygotus by Erik N. Kjellesvig-Waering in 1950. It most closely resembles P. cobbi and P. barrandei , differing from P. cobbi in its more developed central tooth and

3280-607: The early Paleozoic of the Welsh Borderland , including the discovery of important Silurian fossils (such as eurypterids), in the 1800s. This species was one of the most common eurypterid in England during the Ludlow epoch and was quite large and clearly distinct (though it resembles P. barrandei , P. floridanus and P. cobbi in its cheliceral morphology) from other species of the genus, being known from multiple specimens. The most important fossils of P. lightbodyi include

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3360-410: The edge of the front corners. The telson has a pronounced dorsal carina (or keel) running down its center, terminating in a short spine. The Pterygotidae includes the largest known arthropods to have ever lived, with several species surpassing two metres in length (such as Jaekelopterus rhenaniae at 2.5 metres (8.2 ft) and Acutiramus bohemicus at 2.1 metres (6.9 ft)). Though Pterygotus

3440-669: The extended chelicerae are counted (normally they are not) the total length would exceed 2 metres (6.6 ft). P. carmani , from the Devonian of Ohio , likely reached lengths in excess of 1.5 metres (4.9 ft). The species P. cobbi (1.4 metres (4.6 ft)), P. barrandei (1.26 metres (4.1 ft)) and P. denticulatus (1.2 metres (3.9 ft)) also exceeded 1 metre in length. Smaller species include P. floridanus at 90 centimetres (35 in), P. lightbodyi at 75 centimetres (30 in), P. arcuatus at 60 centimetres (24 in), P. bolivianus at 55 centimetres (22 in) and

3520-432: The eyes suggest an assignation to the genus Pterygotus , differing from P. monroensis in being nearly rectangular in shape and with a straight transverse frontal margin. He suggested a relationship with Slimonia , but he did not assigned it due to the lack of more material indicative of the latter. Although it was later placed on the genus Waeringopterus , Samuel J. Ciurca, Jr. and O. Erik Tetlie concluded in 2007 that

3600-568: The family Pterygotidae was erected by John Mason Clarke & Rudolf Ruedemann in 1912 to include the eurypterid genera Pterygotus , Slimonia , Hughmilleria and Hastimima . The three latter genera would be reclassified as members of the Hughmilleriidae by Erik N. Kjellesvig-Waering in 1951, leaving Pterygotus and its former subgenera as the sole pterygotid eurypterids. Though early discoveries of Pterygotus were confined to England and North America, fossil finds throughout

3680-473: The fossil remains of a large fish. The specimens described by Agassiz from England were referred to a species he dubbed Pterygotus problematicus . Agassiz first recognized the true nature of the fossils as arthropod remains five years later in 1844 after having examined more complete fossils recovered in the Old Red Sandstone of Scotland. Although recognizing the fossils of Pterygotus as arthropod

3760-501: The free ramus (the part of the claw that moves) was less prominent than in other species, which has been noted as similar to the distal tooth in the free ramus of Acutiramus cummingsi . Although P. cobbi is based on poor fossil material, only known from a free ramus, it remains recognized as a distinct species on the account of being more similar to certain species discovered in the Czech Republic (such as P. barrandei ) than it

3840-498: The free ramus of P. barrandei is significantly longer than the corresponding tooth in P. cobbi and the teeth of the free ramus of P. barrandei are directed forwards more prominently in general. Fossils of P. barrandei are rare, with fossil finds being confined to a handful of formations of Pridoli age in Bohemia . Known fossils include some incomplete chelicerae and a metastoma. Some additional fossil remains have been assigned to

3920-459: The genus Hygromia . The concept of the type species in zoology was introduced by Pierre André Latreille . The International Code of Zoological Nomenclature states that the original name (binomen) of the type species should always be cited. It gives an example in Article 67.1. Astacus marinus Fabricius, 1775 was later designated as the type species of the genus Homarus , thus giving it

4000-404: The holotype (consisting of most of a chelicera) and two paratypes (including most of the free ramus). The claws of P. lightbodyi are all equipped with vertically placed and very long teeth, most of which curve slightly backwards. The terminal tooth is unusually slender and long in P. lightbodyi , and as with the other teeth slightly curved backwards. Among the more important diagnostic features of

4080-466: The holotype does not really have eyes and is nothing more than an incomplete body segment. Therefore, they regarded the species as a nomen dubium . P. floridanus , recovered from deposits of Lochkovian age in Florida, extended the known range of eurypterids on the continent over 800 km (500 miles) south. Prior to its discovery, eurypterids in North America were only known from the northern parts of

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4160-471: The largest known species, P. grandidentatus , reached a body length of 1.75 metres (5.7 ft). Several other species, notably P. impacatus at 1.65 metres (5.4 ft) and P. anglicus at 1.6 metres (5.2 ft) were similarly gigantic. Pterygotus was surpassed in size by other giant eurypterids. Acutiramus was able to surpass 2 metres (6.6 ft), and Jaekelopterus could reach 2.6 metres (8.5 ft). Many species were considerably smaller than

4240-470: The largest species, P. grandidentatus , reaching a body length of 1.75 metres (5.7 ft), Pterygotus was among the largest known eurypterids to have existed, though some of its close relatives (such as Acutiramus and Jaekelopterus ) surpassed it in length. Though there were a few gigantic species, many species were considerably smaller in size. The smallest species, P. kopaninensis , measured just 50 centimetres (20 in) in length. Pterygotus

4320-423: The largest species, such as P. kopaninensis at 50 centimetres (20 in). Pterygotus may have weighed around 30 kilogramms. Like its close relative Jaekelopterus , Pterygotus was a large and active predator noted for its robust and enlarged cheliceral claws that would have allowed it to puncture and grasp prey and a visual acuity (clarity of vision) comparable to that of modern predatory arthropods. With

4400-482: The most extensively known species of Pterygotus , distinguished from subsequently discovered species by possessing curved terminal teeth and the primary and intermediate teeth being inclined slightly backwards. P. problematicus was also used as the designation for an incomplete chelicera discovered in the Welsh Borderland of western England by John William Salter in 1852 but is in modern times considered

4480-416: The name Homarus marinus (Fabricius, 1775) . However, the type species of Homarus should always be cited using its original name, i.e. Astacus marinus Fabricius, 1775 , even though that is a junior synonym of Cancer grammarius Linnaeus, 1758 . Although the International Code of Nomenclature for algae, fungi, and plants does not contain the same explicit statement, examples make it clear that

4560-439: The name is no longer in use. Instead P. anglicus , based on a number of diagnostic features and properly illustrated in its description by Agassiz in 1844, is considered the type species of Pterygotus . Two further species that remain assigned to the genus to this day would be described from England during the 19th century; P. ludensis of Pridoli (Late Silurian) age and P. arcuatus of Ludlow (Late Silurian) age, along with

4640-471: The name of a genus or subgenus (a " genus-group name "). In the Glossary, type species is defined as The nominal species that is the name-bearing type of a nominal genus or subgenus. The type species permanently attaches a formal name (the generic name) to a genus by providing just one species within that genus to which the genus name is permanently linked (i.e. the genus must include that species if it

4720-464: The process of excavations beneath Melbourne during the construction of new drainage works for the city in 1899. The fragmentary fossils closely resemble fossils of Erettopterus bilobus (classified as a species of Pterygotus at the time), which might make their assignment to Pterygotus questionable. In 2020, the species was marked as a nomen dubium (a dubious species) due to the lack of sufficient diagnostic material to separate P. australis from

4800-499: The pterygotid family. The specimen (PE6173, housed at the Chicago Natural History Museum ) includes the well-preserved anterior half of a chelicera and ramus. The tooth of the ramus are short, wide and conical, all being slightly curved backwards. The terminal tooth is larger, but only slightly, than the tooth succeeding it and the inwards bend of the claw suggests that another tooth might be present, creating

4880-407: The ramus is poorly known from other species of Pterygotus and P. waylandsmithi was reclassified as a species of Erettopterus in 2007 the assignment of P. grandidentatus to Pterygotus is questionable. England would also yield a dubious species, P. taurinus , from deposits of Pridoli or Devonian age. Named by Salter in 1868, P. taurinus is treated as a dubious species for the reason that it

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4960-605: The rest of the pterygotids. Kjellesvig-Waering named the species P. bolivianus in 1964 based on fossils recovered from deposits of Emsian - Eifelian (Early to Middle Devonian) age in Bolivia. This species was the first pterygotid to be discovered in South America, the first Devonian pterygotid to be recovered in deposits in the Southern Hemisphere and also represents one of the last known living member of

5040-409: The scale-like ornamentation characteristic of the group which researchers have wrongfully believed was characteristic of only Pterygotus or P. problematicus . As such ornamentation is known from every pterygotid genus it can not be used as a diagnostic feature of a single species. Though P. problematicus is the earliest name used for a species of Pterygotus , it is not considered the type species as

5120-424: The shape of the eyes and carapace was similar to how these body parts are shaped in Erettopterus . England, the site of the initial discovery of P. problematicus , has provided fossils for several additional species. Kjellesvig-Waering named three new species from England in 1961; P. denticulatus , P. lightbodyi (both Late Ludlow in age) and P. grandidentatus ( Wenlock , Late Silurian, in age). P. denticulatus

5200-537: The smallest known species, P. kopaninensis , at 50 centimetres (20 in) in length. The first fossils of Pterygotus were found in deposits of Lochkovian - Pragian (Early Devonian) age by quarrymen in Scotland and western England, who referred to the large fossil remains as " Seraphims ". Louis Agassiz , a Swiss-American biologist and geologist, described the fossils in 1839 and named it Pterygotus , which translates to "winged one". Agassiz believed that they were

5280-400: The species include the paratype (No. 7059/3, a fragmentary chelicera). This specimen includes several of the features that are diagnostic of P. impacatus , such as upright teeth following the thick and long teeth of the terminal part of the claw. Particularly of diagnostic value is that there are teeth present at the point where the terminal teeth first begin. The central tooth of the free ramus

5360-549: The species is the combination of a large terminal tooth and a large upright tooth near it. P. grandidentatus is known from a single specimen, the anterior half of a free ramus of a chelicera discovered in the Wenlock -aged beds at Dudley in Worcestershire, England (specimen number I. 3163 in the British Museum of Natural History ). It is notable for the stout stem and the unusually long length (1.75 cm, 0.7 in) of

5440-414: The species, consisting of coxae and a genital appendage, but their assignment to the species is doubtful. The species P. nobilis , described in 1872, is based on a small and fragmentary chelicera found in what today is the Czech Republic . The arrangement of teeth seen in this claw, though most teeth are not preserved, was noted by researcher Max Semper in 1897 as sharing little to no resemblance with what

5520-504: The species, such subgenera include Pterygotus ( Curviramus ) and Pterygotus ( Acutiramus ), named in 1935 based upon features of the denticles (teeth) of the chelicerae. Pterygotus ( Curviramus ) was later recognized as synonymous with Pterygotus ( Pterygotus ) by Leif Størmer the same year, and Erettopterus and Acutiramus would be recognized as separate, but closely related, genera ( Erettopterus by Erik N. Kjellesvig-Waering in 1961, and Acutiramus by Størmer in 1974). In 1912,

5600-537: The telson and the spine is blunt. The species is very distinct, being distinguishable from all other Silurian species of Pterygotus by the shape of its telson. A species of Jaekelopterus , J. howelli from the Early Devonian, is similar in the wide and truncated telson shape, but is easily distinguished by possessing serrations and a much larger terminal spine. The species P. monroensis , known from deposits of late Wenlock to Ludlow age in New York State, USA,

5680-462: The telson. Similarities in the genital appendage could mean that the three genera are all synonyms of each other, as they had been classified in the past (as species of Pterygotus ). Some differences between them have also been noted in the chelicerae, though chelicerae have been questioned as the basis of eurypterid generic distinction since their morphology depends on the lifestyles and has been observed to vary throughout ontogeny . Telson morphology

5760-416: The terminal tooth and the unusual thickness of its base. P. grandidentatus can easily be distinguished from other species not only be its unusual terminal tooth, but also by the disoriented teeth along the claw, being bent in a variety of different directions. The terminal part of the ramus ends in an arrangement of multiple teeth otherwise only noted in the species P. waylandsmithi . As this specific part of

5840-492: The type of a genus name is a specimen (or, rarely, an illustration) which is also the type of a species name. The species name with that type can also be referred to as the type of the genus name. Names of genus and family ranks, the various subdivisions of those ranks, and some higher-rank names based on genus names, have such types. In bacteriology , a type species is assigned for each genus. Whether or not currently recognized as valid , every named genus or subgenus in zoology

5920-479: The wide but short and evenly sized teeth as well as the terminal tooth not having any particular development. In 2019, a new fragmentary ramus of a chelicera was found in the Cuche Formation of Colombia . The specimen (SGC-MGJRG.2018.I.5), assigned with uncertainty to P. bolivianus due to similarities with its holotype, represents the first eurypterid of Colombia and the fourth of South America. The fossil

6000-411: Was classified as the separate genus Ciurcopterus in 2007 by O. Erik Tetlie and Derek E. G. Briggs, distinguished primarily by sharing several features with more basal pterygotioid eurypterids, such as its appendages being similar to those of Slimonia . New fossil finds also revealed the presence of Pterygotus in several European countries where it had previously been unknown and established it as

6080-561: Was closer to its modern phylogenetical position, Agassiz would consider Pterygotus to represent a crustacean of the Entomostraca subclass. Although Frederick M'Coy did note that Pterygotus resembled the Limulidae and the previously discovered eurypterid Eurypterus in 1849, he classified both Eurypterus and Pterygotus as crustaceans. The new Scottish fossils were named as the species P. anglicus in 1849, which remains

6160-665: Was dated as Frasnian (Late Devonian), showing that Pterygotus did not become extinct during the Middle Devonian as previously thought. Following close examination and the discovery of new fossil evidence, further genera would be split off from Pterygotus . P. rhenaniae was classified as part of its own genus, Jaekelopterus , by Charles D. Waterston in 1964. He considered the species sufficiently distinct from other Pterygotus species due to its supposedly segmented genital appendage (a feature later realized to be wrong), its narrow and long chelicerae, and its primary teeth being angled slightly anteriorly. Another species, P. ventricosus ,

6240-429: Was not the largest of the pterygotids, several species were large, surpassing 1 metre (3.3 ft) in length. The largest known species was P. grandidentatus , with the largest known isolated chelicerae fragments suggesting a length of 1.75 metres (5.7 ft). The Estonian P. impacatus is the second largest known species, the largest fragmentary remains suggesting a length of 1.65 metres (5.4 ft). P. anglicus ,

6320-505: Was suggested to represent a synonym of Erettopterus osiliensis by Samuel J. Ciurca, Jr. and O. Erik Tetlie in 2007, based upon the similar shape of the eyes and the carapace. Such a reassignment would have implications for other species of Pterygotus as well, with P. impacatus potentially also representing a synonym of E. osiliensis . Subsequent studies and lists of eurypterid species have continued to treat P. monroensis and P. impacatus as distinct species of Pterygotus . Pterygotus

6400-611: Was the second pterygotid to be discovered from the well known eurypterid fauna of Lesmahagow in Lanarkshire, Scotland. As pterygotids commonly occur in association with multiple related genera, it was considered unusual that there was only one species, Erettopterus bilobus , present in Lesmahagow. Fossil remains of P. lanarkensis had been known since 1868 (first collected by Robert Slimon in 1855–1860), but were first recognized as such by Kjellesvig-Waering in 1964. Represented by

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