Basic info Taxonomic history Classification Included Taxa
Morphology Ecology and taphonomy External Literature Search Age range and collections

Ophthalmothule cryostea

Osteichthyes - Plesiosauria - Cryptoclididae

Taxonomy
Ophthalmothule cryostea was named by Roberts et al. (2020) [A moderately sized cryptoclidid plesiosaur (estimated body length of 5.0–5.5 m), possessing the following autapomorphies unique among Cryptoclididae () and unique character combinations: premaxilla bears 6 alveoli (5 in Tricleidus seeleyi and Muraenosaurus leedsii); medial process of premaxilla terminates anterior to the posterior margin of external naris (); maxilla estimated to contain a similar number of alveoli (>16) as in in Cryptoclidus eurymerus (18) and Tricleidus seeleyi (15); frontal twice as anteroposteriorly long as parietal (subequal or shorter in Cryptoclidus eurymerus and M. leedsii); frontal participates in the medial and posterior margins of the external naris (participates posteriorly in M. leedsii); presence of an interfrontal vacuity (absent in M. leedsii); dorsoventrally low but mediolaterally narrow sagittal crest (flat and mediolaterally broad in Kimmerosaurus langhami); quadrate articulates anterolaterally to the pterygoid (posteromedially in Tricleidus seeleyi and M. leedsii); lateral cotyle of quadrate larger than medial cotyle (reversed in S. larseni); basioccipital tubera mediolaterally broad and dorsoventrally flattened (circular in K. langhami and Cryptoclidus eurymerus); basioccipital tubera triangular in ventral view, following the anteromedial process of pterygoid anteriorly (cylindrical with finished bone anteriorly in K. langhami); exoccipital does not contribute to occipital condyle (contributes in K. langhami and Cryptoclidus eurymerus); posteromedian ridge on supraoccipital absent (present in K. langhami and M. leedsii); palatine and vomer excludes maxilla from internal naris (maxilla participates in M. leedsii); vomer excluded from anterior interpterygoid vacuity (participates in M. leedsii and Cryptoclidus eurymerus); anteromedial process of pterygoid extends as far as the parabasisphenoid (absent in Cryptoclidus eurymerus); dentary with a mediolaterally extended alveolar surface and with laterally shifted, labially inclined alveoli (no mediolateral extension and alveoli positioned centrally in Tricleidus seeleyi); deep glenoid facet of the mandible, constituting over half the dorsoventral height of the mandible (relatively shallow in Colymbosaurus spp., Cryptoclidus eurymerus and K. langhami); retroarticular process slightly dorsally inclined (significantly inclined in Spitrasaurus larseni); faint longitudinal ridges on the teeth, distinct on labial side (distinct on lingual side in M. leedsii and Cryptoclidus eurymerus; ridging absent in K. langhami); slightly recurved tooth crowns (significantly recurved in S. larseni and K. langhami); mamillate hypophyseal eminence is present on the ventral surface of the atlas (ventral keel or keel-like morphology in Cryptoclidus eurymerus, M. leedsii and Tricleidus seeleyi); atlantal rib present (absent in Colymbosaurus megadeirus); 50 cervical vertebrae (32 in Cryptoclidus eurymerus; 44 in M. leedsii; 41 in Colymbosaurus megadeirus; 60 in Spitrasaurus wensaasi); cervical centra are slightly amphicoelous (conspicuously concave in Djupedalia engeri and K. langhami); cervical vertebra eight with anteroposteriorly long postzygapophyses, close to the length of centrum (autapomorphic among Plesiosauria); anterior-most cervical neural spines low and posteriorly angled (straight in K. langhami); cervical prezygapophyses unfused anteriorly and fused posteriorly (unfused throughout in Cryptoclidus eurymerus and completely fused in Spitrasaurus spp. and D. engeri); postzygapophyses fused along the midline (unfused in posterior-most cervicals in D. engeri); lateral ridges present on mid-posterior cervicals (absent in Colymbosaurus megadeirus, Cryptoclidus eurymerus, D. engeri, and Tricleidus seeleyi); posterior cervical—anterior dorsal ribs with a distinct, short (North-facing slopes of Wimanfjellet (Mt. Wiman), which is in a Tithonian/Berriasian marine mudstone in the Agardhfjellet Formation of Norway.

Synonymy list
YearName and author
2020Ophthalmothule cryostea Roberts et al.

Is something missing? Join the Paleobiology Database and enter the data

RankNameAuthor
kingdomAnimalia()
Bilateria
EubilateriaAx 1987
Deuterostomia
phylumChordataHaeckel 1874
subphylumVertebrata
superclassGnathostomata
classOsteichthyes
subclassSarcopterygii()
subclassDipnotetrapodomorpha(Nelson 2006)
subclassTetrapodomorpha()
Tetrapoda
Reptiliomorpha
Anthracosauria
RankNameAuthor
subclassAmphibiosauriaKuhn 1967
Cotylosauria()
Amniota
Sauropsida
classReptilia
subclassEureptilia()
Romeriida
Diapsida()
suborderSauropterygia
orderPlesiosauriade Blainville 1835
superfamilyPlesiosauroideaWelles 1943
familyCryptoclididaeWilliston 1925
genusOphthalmothule
speciescryostea

If no rank is listed, the taxon is considered an unranked clade in modern classifications. Ranks may be repeated or presented in the wrong order because authors working on different parts of the classification may disagree about how to rank taxa.

Ophthalmothule cryostea Roberts et al. 2020
show all | hide all
Diagnosis
No diagnoses are available
Measurements
No measurements are available
Composition: hydroxyapatiteo
Environment: marineo
Locomotion: actively mobileo
Life habit: aquatico
Depth habitat: surfaceo
Diet: carnivoreo
Reproduction: viviparouso
Created: 2009-07-20 06:05:48
Modified: 2011-08-12 01:58:15
Source: o = order
Reference: Kiessling 2004

Age range: base of the Tithonian to the top of the Berriasian or 149.20000 to 137.05000 Ma

Collections: one only


Time interval Ma Country or state Original ID and collection number
Tithonian - Berriasian149.2 - 137.05Norway (Spitsbergen) Ophthalmothule cryostea (type locality: 208878)