Unusual morphology in the mid-Cretaceous lizard Oculudentavis
Author
Bolet, Arnau
Institut Català de Paleontologia Miquel Crusafont, Universitat Autònoma de Barcelona, Barcelona, Spain & School of Earth Sciences, University of Bristol, Bristol, UK
Author
Stanley, Edward L.
Department of Natural History, Florida Museum of Natural History, Gainesville, FL, USA
Author
Daza, Juan D.
Department of Biological Sciences, Sam Houston State University, Huntsville, TX, USA
juand.daza@gmail.com
Author
Arias, J. Salvador
Unidad Ejecutora Lillo (CONICET - Fundación Miguel Lillo), San Miguel, de Tucumán, Tucumán, Argentina
Author
Cernanský, Andrej
Department of Ecology, Laboratory of Evolutionary Biology, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia
Author
Vidal-García, Marta
Department of Cell Biology & Anatomy, University of Calgary, Calgary, AB, Canada
Author
Bauer, Aaron M.
Department of Biology and Center for Biodiversity and Ecosystem Stewardship, Villanova University, Villanova, PA, USA
Author
Bevitt, Joseph J.
Australian Centre for Neutron Scattering, Australian Nuclear Science and Technology Organisation, Sydney, NSW, Australia
Author
Peretti, Adolf
GRS Gemresearch Swisslab AG and Peretti Museum Foundation, Meggen, Switzerland
Author
Evans, Susan E.
Department of Cell and Developmental Biology, University College London, London, UK
text
Current Biology
2021
2021-06-14
31
1
12
journal article
10.1016/j.cub.2021.05.040
a0723a89-d4df-4e36-9da9-cc6fd438c7c3
5013953
Genus
Oculudentavis
Xing et al.
1
Type
species
Oculudentavis khaungraae
Xing et al.
1
Note: The retraction
8
of the original description of this taxon
1
does not affect the nomenclatural availability of
Oculudentavis khaungraae
under the International Code of Zoological Nomenclature (chapters 3 and 4), as retraction of a paper by itself has no nomenclatural consequence.
9–11
Using
O. khaungraae
as an example, there have been recommendations that the code needs to be modified to cover names and nomenclatural acts contained in retracted papers and to include a rule that can be applied automatically without the necessity of submitting a case.
12
Nonetheless, at the present time, the current regulations stand.
Diagnosis of the genus
Oculudentavis
Oculudentavis
can be identified as a lizard by having a pleurodont dentition with posterolingual tooth replacement, a short quadrate with a lateral conch, a streptostylic quadrate suspension, a ‘‘hockey stick’’-shaped squamosal, a reduced quadrate-pterygoid contact, an enclosed vidian canal (posterior opening within the basisphenoid), a prootic with an alar process and a prominent crista prootica, and a braincase in which the metotic fissure is subdivided into a small ovoid lateral opening of the recessus scalae tympani and a posterior vagus foramen (differentiating it from archosaurs, where the metotic fissure becomes enclosed, following a totally different development).
13
The genus
Oculudentavis
can be diagnosed by the following apomorphic characters. Some of these characters are reworded here from the original diagnosis of
O. khaungraae
1
and some from a subsequent paper,
3
which now includes characters that only apply to
O
.
khaungraae
: jugal expanded horizontally creating a wide ventral orbital flange; jugal bar cross-section strongly angled dorsolaterally-ventromedially;
1
22 to 23 teeth in maxilla, about four of which are located beneath the orbit; vomers contact both the premaxillary and maxillary shelves; large unpaired median premaxilla with a long dorsal crest along nasal process that is continued onto the dorsal surface of the nasals along most of its length; premaxilla replaces maxilla in anterolateral part of rostrum; ring-shaped lacrimal fully enclosing large lacrimal foramen; short vaulted parietals partially fused; and presence of a flat surface (forming a platform) on the dorsolabial side of the posterior third of the dentary.
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(legend on next page)
Oculudentavis
differs from all other known lizards in possessing the following unique combination of characters: premaxilla forming exclusively the tip of the rostrum and the anterolateral border of the nares; elongated paired nasals that slot into a triangular frontal recess; no parietal foramen, supratemporal processes angled vertically downward; strongly triradiate postorbital with long squamosal process reaching posterior margin of parietal; very large suborbital fenestra; palatal dentition on the pterygoids—differing from the interpretation in Li et al.,
3
which also reported teeth on the palatine, the presence of which we have been unable to confirm; in dentary, dorsal and ventral margins of the Meckelian fossa meet to close fossa, but do not fuse; and short postdentary region with coronoid bearing a low, posteriorly set process, short deep adductor fossa, and long slender retroarticular process.
Oculudentavis
further differs from all squamates except
Huehuecuetzpalli
in having a long tapering rostrum
3
composed of premaxilla, maxillae, and elongated paired nasals that slot into a triangular frontalrecess; from allsquamates except for
Huehuecuetzpalli
, varanids, lanthanotids, monstersaurs, and mosasaurs in theretractednarial openings,
3
although inallbut
Huehuecuetzpalli
a reduction of the nasals occurs; from all squamates except chameleons in having a prefrontal with an anterolateral shelf (‘‘boss’’ in Gauthier et al.
7
) that overhangs maxilla and lacrimal; from all squamates except for the pygopodid
Lialis
in its very long slender mandible composed mainly of shallow elongate dentary and relatively short post-dentary portion; and from all squamates except for some anguimorphs in the presence of posterolingual tooth replacement. The closed (but not fused) Meckelian fossa is shared mainly with iguanians, differing from the open fossa of most anguimorphs, lacertoids, and scincoids and the closed and fused fossa of gekkotans, dibamids, gymnophthalmids, xantusiids, some scincids, and some iguanians.
Thepremaxilla,maxilla,andnasalare notfusedinto asingle unit as was described in the original description of
O. khaungraae
.
1