PROFILPELAJAR.COM

Nectridea; Temporal range: Late Carboniferous–Lopingian PreꞒ Ꞓ O S D C P T J K Pg N
	Skeleton and model of Diplocaulus.
Scientific classification
Domain:	Eukaryota
Kingdom:	Animalia
Phylum:	Chordata
Clade:	Sarcopterygii
Clade:	Tetrapodomorpha
Clade:	Stegocephali
Order:	†Nectridea; Miall, 1875
Subgroups
	Arizonerpeton; Diplocaulidae; Scincosauridae; Urocordylidae;

Nectridea is the name of an extinct order of lepospondyl tetrapods from the Carboniferous and Permian periods, including animals such as Diplocaulus. In appearance, they would have resembled modern newts or aquatic salamanders, although they are not close relatives of modern amphibians.^[1] They were characterized by long, flattened tails to aid in swimming, as well as numerous features of the vertebrae.

Description

A life restoration of *Urocordylus*, a urocordylid

Nectrideans are a diverse group of tetrapods, including the aquatic Urocordylidae, the presumably terrestrial Scincosauridae, and the bizarre horned members of Diplocaulidae (also known as Keraterpetonidae), which includes the "boomerang-headed" Diplocaulus, one of the most famous genera of prehistoric amphibians (in the traditional sense of the word). By the time the earliest known nectrideans appeared in the Late Carboniferous fossil record, they had already diversified into these families, indicating that basal nectrideans are unknown. These different families are united primarily by features of the spinal column rather than the skull.

Vertebrae

In many groups of early tetrapods, each vertebra is formed by three parts: an intercentrum at the front, a pleurocentrum at the back, and a plate-like neural spine jutting out from the top of the vertebrae which may be positioned between the two or fused to the pleurocentrum. In nectrideans, only the pleurocentra are present, and the neural spines are completely fused to them. Their vertebrae also possess an extra set of joints connecting the vertebrae (apophyses), just above the typical set (zygapophyses). Furthermore, their caudal (tail) vertebrae also possess haemal spines which jut out from the bottom of each vertebra. While most early tetrapods have slanted haemal spines which are positioned between the vertebrae, the haemal spines of nectrideans are completely vertical in orientation and fused to the pleurocentra, directly opposite the neural spines. Both the neural spines and haemal spines of the tail are characteristically fan-shaped. As a whole, nectrideans have rather short bodies and long and paddle-like tails, adapted for swimming.^[2]^[1]

Other features

Almost all early tetrapods have three coronoid bones lining the inside edge of each side of the jaw. Nectrideans, however, only have one. Their clavicular blades (shoulder girdles) are wide and possess a short rear extension, while the scapulocoracoids (shoulder blades) are weakly ossified.^[2]

They also had well-developed hind limbs, with a full set of five toes each. Their forelimbs were slightly reduced, but not to the same extent as in microsaurs and other lepospondyls. Although Urocordylus retained five fingers, most nectridieans had only four, similar to modern amphibians.^[2]^[3]

Life restoration of *Scincosaurus*, a scincosaurid

Paleobiology

Both diplocaulids and urocordylids are considered to be completely aquatic, although only diplocaulids possess lateral line canals on their skulls. However, this does not mean that urocordylids lacked lateral lines, as several modern amphibians possess that organ without any skeletal indication. Scincosaurids have much more well-ossified limbs and thinner tails than other nectrideans, and are usually considered to be terrestrial. However, some have been reported to possess lines of pits on the skull, which may be an indication that they were amphibious rather than purely terrestrial.^[4]

A trace fossil known as Hermundurichnus fornicatus of a tetrapod resting on a lake bed may have been attributed to Diplocaulus or an animal like it. This trace indicates that the underside of nectrideans was covered in small, diamond-shaped scales and that the "horns" of the skull were connected with the body by flaps of skin.^[5]

Classification

There has been some controversy over the precise classification of Nectridea over the past century, and even whether it constitutes a valid monophyletic clade. A few older studies consider nectrideans to be very basal tetrapods, related to Ichthyostega or colosteids. However, most studies generally place nectrideans inside the subclass Lepospondyli. Aistopoda, a group of legless lepospondyls, have often been allied with particular families of nectrideans, but not the order as a whole. For example, Anderson (2001) positioned diplocaulids as close relatives of Aistopods with urocordylids and scincosaurids as progressively more primitive members of the group. On the other hand, Ruta et al. (2003) claimed that urocordylids were closer to aistopods. As aistopods do not possess most nectridean features, they have traditionally been excluded from the group. However, this would make Nectridea an invalid paraphyletic group as the aistopods, may have been descended from nectrideans, are not considered nectrideans themselves.^[6]

The following is a cladogram from the Ruta et al. (2003):

Lepospondyli

	Batropetes fritschi

	Tuditanomorpha

Microbrachis pelikani

	Hyloplesion longicostatum

	Odonterpeton triangulare

Lysorophia

Adelospondyli

Holospondyli

	Aistopoda

	Urocordylidae

	Diplocaulidae

	Scincosauridae

"Nectridea"

References

^ ^a ^b Milner, Andrew R. (1993). "The Paleozoic Relatives of Lissamphibians". Herpetological Monographs. 7: 8–27. doi:10.2307/1466948. JSTOR 1466948.
^ ^a ^b ^c Carroll, R. L. (2009). The rise of amphibians. The Johns Hopkins University Press.
^ Palmer, D., ed. (1999). The Marshall Illustrated Encyclopedia of Dinosaurs and Prehistoric Animals. London: Marshall Editions. p. 54. ISBN 1-84028-152-9.
^ Vallin, Grégoire; Laurin, Michel. "Cranial morphology and affinities ofMicrobrachis, and a reappraisal of the phylogeny and lifestyle of the first amphibians". Journal of Vertebrate Paleontology. 24 (1): 56–72. doi:10.1671/5.1.
^ Lockey, Martin; Meyer, Christian (2000). Dinosaur Tracks and other Fossil Footprints of Europe. Columbia University Press.
^ Marcello Ruta, Michael I. Coates and Donald L. J. Quicke (2003). "Early tetrapod relationships revisited" (PDF). Biological Reviews. 78 (2): 251–345. doi:10.1017/S1464793102006103. PMID 12803423.

Ahlberg, P. E. & Milner, A. R. 1994: The origin and early diversification of tetrapods. Nature: vol. 368, 7 April, pp. 507–514
Anderson, J. S. 1998: Phylogenetic analysis of the Lepospondyli (Tetrapoda). Journal of Vertebrate Paleontology. Vol. 18, #3, Suppl. to #3, pp. 24A
Carroll, R. L., 1988: Vertebrate paleontology and evolution. W. H. Freeman and company, New York, 1988, 698.
Carroll, R. L., 1988: Appendix. 594-648. in Carroll, R. L., 1988: Vertebrate paleontology and evolution. W. H. Freeman and company, New York, 1988, 698.
Carroll, R. L. 1996: Revealing the patterns of macroevolution. Nature: vol. 381, 2 May, pp. 19–20
Clack, J. A., 1998: A new Early Carboniferous tetrapod with a mélange of crown-group characters. Nature: vol. 394, 2 July, pp. 66–69
Shubin, N., 1998 [preview]: Evolutionary cut and paste. Nature: vol. 394, 2 July, pp. 12–13
Vallin, G. & Laurin, M., 2004: Cranial morphology and affinities of Microbrachis, and a reappraisal of the phylogeny and lifestyle of the first amphibians. Journal of Vertebrate Paleontology: Vol. 24, #1, pp. 56–72