Dissorophidae

Dissorophidae is an extinct family of medium-sized, temnospondyl amphibians that flourished during the late Carboniferous and early Permian periods. The clade is known almost exclusively from North America.

History of study

Dissorophidae is a diverse clade that was named in 1902 by George A. Boulenger. Junior synonyms include Otocoelidae, Stegopidae, and Aspidosauridae. Early in the study of dissorophoids when the relationships of different taxa were not well-resolved and most taxa had not been described, Dissorophidae sometimes came to include taxa that are now not regarded as dissorophids and may have excluded earlier described taxa that are now regarded as dissorophids. Amphibamiforms were widely regarded as small-bodied dissorophids, and at one point, Dissorophidae was also suggested to also include Trematopidae.

19th century

In 1895, American paleontologist Edward Drinker Cope named ''Dissorophus'' from the early Permian of Texas. This was the first dissorophid to be described as such, although ''Parioxys'', named by Cope in 1878, and ''Zygosaurus'', named by the Russian paleontologist Karl von Eichwald in 1848, have also been regarded as dissorophids. A second species of ''Dissorophus'' as well as both species of the genus ''Otocoelus'' that were all named in 1896 by Cope in two papers are now regarded as junior synonyms of the type species of ''Dissorophus'', ''D. multicinctus''.

20th century

The early 20th century saw a large expansion in the study of dissorophids. In 1904, German paleontologist Ferdinand Broili named the first species of ''Aspidosaurus, A. chiton'', from the early Permian of Texas. Additional species of ''Aspidosaurus'' were named shortly thereafter, including ''Aspidosaurus glascocki'' from the early Permian of Texas and ''Aspidosaurus novomexicanus'' from the late Carboniferous of New Mexico. A third species, "''Aspidosaurus crucifer''" described by American paleontologist E.C. Case is now regarded as an indeterminate aspidosaurine. In 1910, two of the best-known dissorophid genera were named: ''Cacops aspidephorus'' and ''Platyhystrix'' (as a species of '' Ctenosaurus''; proper name erected in 1911). Case also provided new information on ''Dissorophus'' in 1910''.'' In 1911, Case named ''Alegeinosaurus aphthitos'' from the early Permian of Texas. In 1914, Samuel W. Williston described the first species of ''Broiliellus'', ''B. texensis''. Additional information on ''Parioxys ferricolus'' was provided in two studies by Egyptian paleontologist Y.S. Moustafa in 1955.

The 1960s were a particular productive time for dissorophid research. In two separate papers published in 1964, Canadian paleontologist Robert L. Carroll named four new taxa: '' Brevidorsum profundum, Broiliellus brevis'', and '' Parioxys bolli'' from the early Permian of Texas and ''Conjunctio multidens'' from the early Permian of New Mexico. Conjunctio was named from a specimen originally referred to ''Aspidosaurus novomexicanus'' by Case et al. (1913) that was also placed in ''Broiliellus'' by American paleontologist Wann Langston in 1953 before being divided again by Carroll. In 1965, American paleontologist E.C. Olson described the first and only middle Permian dissorophid from North America, '' Fayella chickashaensis'', on the basis of an isolated braincase and isolated fragments. A large postcranial skeleton from a different locality was referred to this taxon by Olson in 1972. In 1966, American paleontologist Robert E. DeMar named a new taxon, "''Longiscitula houghae''" from the early Permian of Texas; this is now regarded as a junior synonym of ''Dissorophus multicinctus'' by British paleontologist Andrew Milner. DeMar also provided the first synthesis of the morphological diversity and possible function of dissorophid osteoderms in 1966 and named two new species of ''Broiliellus'' in 1967, ''B. arroyoensis'' and ''B. olsoni'', and completed a detailed revision of ''D. multicinctus'' in 1968.

In 1971, American paleontologist Peter Vaughn described one of the few dissorophids outside of New Mexico, Texas, and Oklahoma, '' Astreptorhachis ohioensis'' from the late Carboniferous of Ohio, represented by a series of fused neural spines and osteoderms. American paleontologist John Bolt published a survey of dissorophid osteoderms in 1974 with an emphasis on taxonomic utility and differentiation and reports of material from the early Permian Richards Spur locality in Oklahoma; in 1977, Bolt reported ''Cacops'' from the locality. In 1980, Russian paleontologist Yuri Gubin described two new middle Permian dissorophids from Russia: '' Iratusaurus vorax'' and '' Kamacops acervalis''. The most complete cranial material of ''Platyhystrix rugosus'' was described in 1981 by a team led by American paleontologist David Berman. Additional postcranial material of ''Platyhystrix'', primarily the characteristic hyperelongate spines, was also periodically reported. The revision of ''Ecolsonia cutlerensis'' in 1985 by Berman and colleagues placed the taxon as a dissorophid, but this taxon is more often recovered as a trematopid. In 1999, Chinese paleontologists Li Jinling and Cheng Zhengwu described the first and only dissorophid from eastern Asia, the middle Permian '' Anakamacops petrolicus'' from China.

21st century

In 2003, American paleontologists Berman and Spencer G. Lucas named a new species of ''Aspidosaurus'' from Texas, ''A. binasser''. Two papers on the osteoderm biomechanics of ''Cacops aspidephorus'' and ''Dissorophus multicinctus,'' led by Canadian paleontologist David Dilkes, were published in 2007 and 2009. In 2009, a team led by Canadian paleontologist Robert Reisz described a new species of ''Cacops, C. morrisi'', from the Richards Spur locality; additional material of this taxon was described in 2018 by American paleontologist Bryan M. Gee and Reisz. A second species from the locality was described in 2012 by German paleontologist Nadia B. Fröbisch and Reisz, ''C. woehri''; additional material of ''Cacops woehri'' was described in 2015 by a team led by Fröbisch. A team led by German paleontologist Florian Witzmann published a comparative histology study that sampled a number of dissorophids in 2010. May et al. (2011) described material of ''Aspidosaurus'' from the late Carboniferous of the mid-continent of North America. The first phylogenetic review of the Dissorophidae was published in 2012 by Schoch. In 2013, three new dissorophids were named in a festschrift dedicated to Reisz in Comptes Rendus Palévol: ''Broiliellus reiszi'' from the early Permian of New Mexico in a study led by Canadian paleontologist Robert Holmes; '' Scapanops neglecta'' from the early Permian of Texas in a study by German paleontologists Schoch and Hans-Dieter Sues, re-evaluating a specimen historically referred to as the Admiral Taxon; and '' Reiszerpeton renascentis'' from the early Permian of Texas in a review of material referred to the amphibamiform '' Tersomius texensis'' by a team led by Canadian paleontologist Hillary C. Maddin. In 2018, Chinese paleontologist Liu Jun provided an updated osteology of ''Anakamacops'' based on substantially more complete material and erected the tribe Kamacopini to group the middle Permian dissorophids from Eurasia. Two separate studies led by Gee were also published that year, one reappraising the early Permian ''Alegeinosaurus aphthitos'' from Texas, which he suggested to be a junior synonym of ''Aspidosaurus'', and another reappraising the middle Permian ''Fayella chickashaensis'' from Oklahoma, in which the authors determined that the holotype was a nomen dubium but that the referred specimen was sufficiently distinct to warrant erecting a new taxon, ''Nooxobeia gracilis''. Also in 2018, Gee and Reisz reported postcrania of a large indeterminate dissorophid from Richards Spur, which was followed by another study the following year by a team led by Gee that reported extensive new material from several dissorophids from Richards Spur, including the first documentation of ''Aspidosaurus'' and ''Dissorophus'' from the locality.

Anatomy

Dissorophids are most readily recognized for their distinctive osteoderms, although these are not unique to either dissorophids among temnospondyls or to temnospondyls among early tetrapods. It is also debated whether ''Platyhystrix'' has true osteoderms or simply ornamented neural spines with similar morphology to the ornamentation of osteoderms in other taxa. There is also great variability in the osteoderms, both in the number of series and in the overall proportions and anatomy. Dissorophines like ''Dissorophus'' typically possess wide osteoderms in contrast to eucacopines like ''Cacops''. Both groups have two series of osteoderms that are relatively flat, in contrast to aspidosaurines, which purportedly a single series that is dorsally keeled to form an inverted-V morphology; it has been suggested, based on CT data, that at least some aspidosaurines may actually have two series of osteoderms but that one is largely obscured. Although osteoderm morphology has been shown to not exert a discernible influence on dissorophid phylogeny, osteoderms remain a major hallmark used to differentiate major clades within Dissorophidae and remain useful for establishing the monophyly of the group within Dissorophoidea. Schoch & Milner (2014) list several features that diagnose dissorophids, but most of these are only useful for differentiating the clade from the closely related trematopids, and some are outdated in light of newer research: (1) maxillary tooth row terminating at or anterior to the posterior orbital margin; (2) basipterygoid region firmly sutured; (3) no prefrontal-postfrontal contact; (4) absence of denticles on the basal plate of the parasphenoid; (5) no pterygoid-vomer contact; (6) short postorbital; (7) long and parallel-sided choana; and (8) absence of a supinator process.

Aspidosaurines and platyhystricines are represented largely by postcranial material, and thus features such as osteoderms are some of the only differentiators for these taxa, but dissorophines and eucacopiens also have many cranial differences, such as the relative proportions of the skull. Most dissorophids are medium-sized, being intermediate between the small amphibamiforms and the larger trematopids, but Dissorophidae includes the largest known dissorophoids, all from the middle Permian of Eurasia, with skull lengths exceeding 30 cm.

Fossil range

Below is a timeline of the known fossil ranges of dissorophids.

ImageSize = width:700px height:auto barincrement:15px
PlotArea = left:10px bottom:50px top:10px right:10px

Period = from:-310 till:-251
TimeAxis = orientation:horizontal
ScaleMajor = unit:year increment:10 start:-310
ScaleMinor = unit:year increment:5 start:-310
TimeAxis = orientation:hor
AlignBars = justify

Colors =
#legends
id:CAR value:claret
id:ANK value:rgb(0.4,0.3,0.196)
id:HER value:teal
id:HAD value:green
id:OMN value:blue
id:black value:black
id:white value:white
id:paleozoic value:rgb(0.6,0.75,0.55)
id:carboniferous value:rgb(0.4,0.65,0.6)
id:permian value:rgb(0.94,0.25,0.24)

BarData=
bar:eratop
bar:space
bar:periodtop
bar:space
bar:NAM1
bar:NAM2
bar:NAM3
bar:NAM4
bar:NAM5
bar:NAM6
bar:NAM7
bar:NAM8
bar:NAM9
bar:NAM10
bar:NAM11
bar:NAM12
bar:NAM13
bar:NAM14
bar:NAM15
bar:NAM16
bar:NAM17
bar:NAM18
bar:NAM19
bar:NAM20
bar:NAM21
bar:NAM22
bar:NAM23
bar:NAM24

bar:space
bar:period
bar:space
bar:era

PlotData=
align:center textcolor:black fontsize:M mark:(line,black) width:25
shift:(7,-4)

bar:periodtop
from: -310 till: -299 color:carboniferous text:Carboniferous
from: -299 till: -251 color:permian text:Permian

bar:eratop
from: -310 till: -251 color:paleozoic text:Paleozoic Era

PlotData=
align:left fontsize:M mark:(line,white) width:5 anchor:till align:left

color:carboniferous bar:NAM1 from:-308 till:-303.9 text: Astreptorhachis ohioensis
color:carboniferous bar:NAM2 from:-302.3 till:-302 text: cf. Platyhystrix
color:carboniferous bar:NAM3 from:-301 till:-300.7 text: cf. Aspidosaurus
color:carboniferous bar:NAM4 from:-301 till:-297.5 text: Platyhystrix rugosus
color:carboniferous bar:NAM5 from:-300 till:-298 text: Aspidosaurus novomexicanus
color:permian bar:NAM6 from:-294.6 till:-277 text: Aspidosaurus sp.
color:permian bar:NAM7 from:-294 till:-290.7 text: Brevidorsum profundum
color:permian bar:NAM8 from:-293 till:-278.5 text:Conjunctio multidens
color:permian bar:NAM9 from:-290.3 till:-284.7 text: Broiliellus brevis
color:permian bar:NAM10 from:-290.3 till:-284.7 text: Dissorophus angustus
color:permian bar:NAM11 from:-278.7 till:-277.2 text: Conjunctio sp.
color:permian bar:NAM12 from:-277.1 till:-275.9 text: Broiliellus texensis
color:permian bar:NAM13 from:-274 till:-272.5 text: Aspidosaurus chiton
color:permian bar:NAM14 from:-274 till:-272.5 text: Aspidosaurus binasser
color:permian bar:NAM15 from:-274 till:-272.5 text: Broiliellus arroyoensis
color:permian bar:NAM16 from:-274 till:-272.5 text: Dissorophus multicinctus
color:permian bar:NAM17 from:-274 till:-271 text:Cacops morrisi
color:permian bar:NAM18 from:-272.5 till:-270.9 text:Cacops aspidephorus
color:permian bar:NAM19 from:-270.9 till:-269.9 text: Nooxobeia gracilis
color:permian bar:NAM20 from:-269.8 till:-268 text: Anakamacops petrolicus
color:permian bar:NAM21 from:-269.8 till:-268 text: Iratusaurus vorax
color:permian bar:NAM22 from:-269.8 till:-268 text: Kamacops acervalis
color:permian bar:NAM23 from:-269.8 till:-268 text: Zygosaurus lucius

PlotData=
align:center textcolor:black fontsize:M mark:(line,black) width:25

bar:period
from: -310 till: -299 color:carboniferous text:Carboniferous
from: -299 till: -251 color:permian text:Permian

bar:era
from: -310 till: -251 color:paleozoic text:Paleozoic Era

Relationships

Four subfamilies comprise the various dissorophids. Eucacopine (sensu Schoch & Sues, 2013) was traditionally referred to as Cacopinae and includes ''Cacops'' and the middle Permian Eurasian taxa (''Anakamacops, Iratusaurus, Kamacops, Zygosaurus''). Dissorophinae includes ''Dissorophus'' and all four species of ''Broiliellus''. These are the two most widely utilized distinctions within Dissorophidae, although Aspidosaurinae (which includes only ''Aspidosaurus'' and indeterminate ''Aspidosaurus''-like material) was recently revived along with the erection of the new Platyhystricinae (''Platyhystrix'' and ''Astreptorhachis''). The placement of some more poorly known (''Brevidorsum'') or anatomically distinct (''Scapanops'') taxa is less resolved.

Phylogeny

Below is a cladogram from Schoch (2012):

Gallery

Platyhystrix BW.jpg, '' Platyhystrix rugosus'', a platyhystricine of the very late Carboniferous to early Permian of North America
Nooxobeia gracilis (cropped).jpg, '' Nooxobeia gracilis'', an unusually long-legged dissorophid of the early Permian of Oklahoma
Broiliellus olsoni.jpg, '' Broiliellus olsoni'', a dissorophine of the early Permian of Texas
Cacops1DB.jpg, ''Cacops aspidephorus'', a eucacopine of the early Permian of Texas
Zygosaurus14DB.jpg, '' Zygosaurus lucius'', a eucacopine of the middle Permian of Russia
Kamakops1DB.jpg, '' Kamacops acervalis'', a eucacopine of the middle Permian of Russia
Anakamacops petrolicusDB20.jpg, '' Anakamacops petrolicus'', a eucacopine of the middle Permian of China

References

{{Taxonbar, from=Q2463801

Prehistoric amphibian families
Carboniferous temnospondyls
Permian temnospondyls
Pennsylvanian first appearances
Lopingian extinctions
Taxa named by George Albert Boulenger