Weigeltisaurus

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Weigeltisaurus
Temporal range: Lopingian
~260.4–251  Ma
SMNK-PAL 2882.png
Specimen SMNK-PAL 2882
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Family: Weigeltisauridae
Genus: Weigeltisaurus
Kuhn, 1939 [1]
Species:
W. jaekeli
Binomial name
Weigeltisaurus jaekeli
(Weigelt, 1930)
Synonyms
  • Palaeochamaeleo jaekeli
    Weigelt, 1930
  • Gracilisaurus ottoi
    Weigelt, 1930
  • Coelurosauravus jaekeli
    – Evans and Haubold, 1987

Weigeltisaurus is an extinct genus of weigeltisaurid reptile from the Late Permian Kupferschiefer of Germany and Marl Slate of England. It has a single species, originally named as Palaechamaeleo jaekeli in 1930 and later assigned the name Weigeltisaurus jaekeli in 1939, when it was revealed that Palaeochamaeleo was a preoccupied name. A 1987 review by Evans and Haubold later lumped Weigeltisaurus jaekeli under Coelurosauravus as a second species of that genus. [2] A 2015 reassessment of skull morphology study substantiated the validity of Weigeltisaurus and subsequent authors have used this genus. [3] [4] Like other Weigeltisaurids, they possessed long rod-like bones that radiated from the trunk that were likely used to support membranes used for gliding, similar to extant Draco lizards.

Contents

History of discovery

Holotype specimen (SSWG 113/7) Holotype skeleton of Weigeltisaurus jaekeli.png
Holotype specimen (SSWG 113/7)

The first remains of Weigeltisaurus jaekeli were described by Johannes Weigelt in 1930 from a specimen (SSWG 113/7) found in the Kupferschiefer near the town of Eisleben in Saxony-Anhalt, Germany. The specimen was purchased from a fossil dealer in 1913 by Otto Jaekel. Jaekel had considered the bony rods to be caudal fin spines of the coelacanth Coelacanthus granulatus that was also known from the Kupferschiefer, and so the rods were prepared away to expose the skeleton. Johannes Weigelt named the new species Palaeochamaeleo jaekeli both in honour of Jaekel and in reference to the similarity of the skull morphology to those of chameleons.

The same year, Friedrich von Huene noted the similarity of the specimen to Coelurosauravus elivensis from Madagascar, which had been described by Jean Piveteau in 1926, and concluded that both animals were closely related and represented climbing reptiles. In 1939, Oskar Kuhn noted that Palaeochamaeleo had already been used in a different publication in 1903, and proposed the new genus name Weigeltisaurus in honour of Weigelt.

In publications in 1976 and 1986, Günther Schaumberg described additional specimens of Weigeltisaurus from the Kupferschiefer of Germany. Due to the fact that the bony rods were also present on these skeletons, and the fact that the rods were only superficially similar to coelacanth spines, Schaumberg (1976) argued that they represented parts of the animals skeleton and were used for gliding flight, stating that the presence of the bones "...virtually provokes the attempt to explain its function for flight characteristics.". [5] In 1979, a specimen (TWCMS B5937.1) was described from Eppleton Quarry near Hetton-le-Hole, in Tyne and Wear in Northern England, in sediments that are part of the Marl Slate, a unit equivalent to the Kupferschiefer. [6] This specimen was given a detailed description by Susan E. Evans in 1982, in the publication she placed Coelurosauravus and Weigeltisaurus into the new family Coelurosauravidae.

In 1987, Evans and Haubold proposed that Weigeltisaurus jaekeli represented a species of Coelurosauravus, and synonymised Gracilisaurus ottoi, which had been described from a disarticulated postcranial skeleton from the Kupferschiefer by Weigelt in 1930 with Weigeltisaurus jaekeli.

In 2007, Schaumberg, Unwin and Brandt presented and discussed new skeleton details of Weigeltisaurus, the mechanism of unfolding and folding the patagium and presented thin-sections of the rods with lamellar bone.

In 2015 in two separate publications, V. V. Bulanov & A. G. Sennikov redescribed Coelurosauravus elivensis and Coelurosauravus jaekeli and concluded that the generic separation should be maintained, restoring Weigeltisaurus as a valid genus.

In 2021, an extensive description of a mostly complete specimen of Weigeltisaurus (SMNK-PAL 2882) was published, this specimen was collected in 1992 from near the town of Ellrich in Saxony-Anhalt, and had briefly been described in a 1997 publication in Science . [7] [8] The counterpart of the specimen is in private collection and inaccessible to researchers. [7]

List of specimens

Description

Schematic reconstruction of the skeleton of Weigeltisaurus jaekeli Weigeltisaurus jaekeli diagram.png
Schematic reconstruction of the skeleton of Weigeltisaurus jaekeli

Like other weigeltisaurids, the skull and lower jaws of Weigeltisaurus are covered in horns and tubercles, including a horned cranial frill present on both the parietal and squamosal bones. In contrast to the condition in Coelurosauravus and Glaurung, where only tubercles are present on the parietal. [7] The teeth are slightly heterodont, with the front teeth being small and peg-like, while the back teeth are lance-shaped and recurved. [7] The hands and feet have elongate phalanges, similar to those of extant arboreal lizards. [7] At least 22 caudal vertebrae are present on the skeleton, the posterior caudal vertebrae have elongated centra, similar to those of extant lizards. [7] The bones are largely hollow, exhibiting a high skeletal pneumaticity, with the outer cortical bone often less than 1 millimetre (364 in) thick. A minimum of 24 pairs of elongate bony rods are present along the trunk of Weigeltisaurus. They are not ribs, but distinct bones, dubbed "patagials". They have been proposed to represent either modified gastralia (unmodified gastralia are also present on the skeleton) or novel bone ossifications. These rise in length posteriorly until the eighth and longest patagial, with subsequent patagials gradually decreasing in size. [7]

Gliding

Artistic reconstruction of Weigeltisaurus jaekeli Weigeltisaurus reconstruction.png
Artistic reconstruction of Weigeltisaurus jaekeli

The gliding membrane of weigeltisaurids is distinct from those of other gliding reptiles, which originate from modified ribs originating from the upper-lateral surface of the body. In contrast, in weigeltisaurids, the rods originate from the lower-lateral surface of the body. The furling and unfurling of the gliding membrane were likely controlled by the abdominal muscles. Preserved fossils show that the bony rods had a high degree of flexibility, similar to the ribs of living gliding lizards. Due to the low-wing configuration, it is likely that the gliding surface was angled upwards to increase stability. [7] In living gliding lizards, it has been found that the forelimbs grab hold of the front of the membrane during takeoff, and are used to adjust the trajectory mid-flight. Similar behaviour has been proposed for weigeltisaurids. [9] In a 2011 study comparing Coelurosauravus and other extinct gliding reptiles to modern Draco species, Coelurosauravus was found to be a less efficient glider due to its larger body size, with a steep descent angle of over 45 degrees and a consequent substantial drop in height per glide. [7] [10]

Paleoenvironment

The Kupferschiefer and the equivalent Marl Slate is a marine unit that forms part of the Zechstein, a sequence of rocks formed on the edge of the Zechstein Sea, a large inland shallow sea that existed in Northern Europe during the Late Permian. The environment at the time of deposition is considered to have been semi-arid. The terrestrial flora of the Zechstein is dominated by conifers, with seed ferns also being common, while taeniopterids, ginkgophytes and sphenophytes are rare. Other terrestrial vertebrates found in the Kupfershiefer and lower Zechstein include the fellow weigeltisaurid Glaurung, the early archosauromorph Protorosaurus , the pareiasaur Parasaurus, the cynodont Procynosuchus, and indeterminate captorhinids, dicynodonts and dissorophid temnospondyls. [11] [12] [13]

Related Research Articles

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<span class="mw-page-title-main">Neodiapsida</span> Clade of reptiles

Neodiapsida is a clade, or major branch, of the reptilian family tree, typically defined as including all diapsids apart from some early primitive types known as the araeoscelidians. Modern reptiles and birds belong to the neodiapsid subclade Sauria.

<i>Edaphosaurus</i> Extinct genus of synapsids

Edaphosaurus is a genus of extinct edaphosaurid synapsids that lived in what is now North America and Europe around 303.4 to 272.5 million years ago, during the Late Carboniferous to Early Permian. American paleontologist Edward Drinker Cope first described Edaphosaurus in 1882, naming it for the "dental pavement" on both the upper and lower jaws, from the Greek edaphos έδαφος and σαῦρος ("lizard").

<i>Protorosaurus</i> Extinct genus of reptiles

Protorosaurus is an extinct genus of reptile. Members of the genus lived during the late Permian period in what is now Germany and Great Britain. Once believed to have been an ancestor to lizards, Protorosaurus is now known to be one of the oldest and most primitive members of Archosauromorpha, the group that would eventually lead to archosaurs such as crocodilians and dinosaurs.

<i>Petrolacosaurus</i> Genus of tetrapods

Petrolacosaurus is an extinct genus of diapsid reptile from the late Carboniferous period. It was a small, 40-centimetre (16 in) long reptile, and one of the earliest known reptile with two temporal fenestrae. This means that it was at the base of Diapsida, the largest and most successful radiation of reptiles that would eventually include all modern reptile groups, as well as dinosaurs and other famous extinct reptiles such as plesiosaurs, ichthyosaurs, and pterosaurs. However, Petrolacosaurus itself was part of Araeoscelida, a short-lived early branch of the diapsid family tree which went extinct in the mid-Permian.

<i>Coelurosauravus</i> Extinct genus of reptiles

Coelurosauravus is an extinct genus of gliding reptile, known from the Late Permian of Madagascar. Like other members of the family Weigeltisauridae, members of this genus possessed long, rod-like ossifications projecting outwards from the body. These bony rods were not extensions of the ribs but were instead a feature unique to weigeltisaurids. It is believed that during life, these structures formed folding wings used for gliding flight, similar to living gliding Draco lizards.

<span class="mw-page-title-main">Avicephala</span> Extinct clade of neodiapsid reptiles

Avicephala is an extinct, potentially polyphyletic grouping of diapsid reptiles that lived during the Late Permian and Triassic periods characterised by superficially bird-like skulls and arboreal lifestyles. As a clade, Avicephala is defined as including the gliding weigeltisaurids and the arboreal drepanosaurs to the exclusion of other major diapsid groups. This relationship is not recovered in the majority of phylogenetic analyses of early diapsids and so Avicephala is typically regarded as an unnatural grouping. However, the clade was recovered again in 2021 in a redescription of Weigeltisaurus, raising the possibility that the clade may be valid after all.

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Rautiania is an extinct genus of gliding neodiapsid reptiles belonging to the family Weigeltisauridae. Isolated fossil remains of Rautiania are known from the Late Permian of Russia. The genus is known from two species, Rautiania alexandri and Rautiania minichi, which differ in aspects of their maxilla and parietal bones. Certain Rautiania fossils have helped to reveal certain aspects of weigeltisaurid anatomy and lifestyle which had long alluded paleontologists, such as the component bones of the "crest" at the back of the head, and the large amount of adaptations towards life in the canopies of forests.

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Weigeltisauridae is a family of gliding neodiapsid reptiles that lived during the Late Permian, between 259.51 and 251.9 million years ago. Fossils of weigeltisaurids have been found in Madagascar, Germany, Great Britain, and Russia. A possible weigeltisaurid, Wapitisaurus, been found in Early Triassic strata in North America, but its poor preservation makes referral to the group questionable. They are characterized by long, hollow rod-shaped bones extending from the torso that probably supported wing-like membranes. Similar membranes are also found in several other extinct reptiles such as kuehneosaurids and Mecistotrachelos, as well as living gliding lizards, although each group evolved these structures independently.

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References

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