Oldest southern sauropterygian reveals early marine reptile globalization.

Sauropterygians were the stratigraphically longest-ranging clade of Mesozoic marine reptiles with a global fossil record spanning ∼180 million years1. However, their early evolution has only been known from what is now the Northern Hemisphere, extending across the northern and trans-equatorial western margins of the Tethys paleo-ocean1 after the late-Early Triassic (late Olenekian, ∼248.8 million years [Ma] ago2), and via possible trans-Arctic migration1 to the Eastern Panthalassa super-ocean prior to the earliest Middle Triassic (Olenekian-earliest Anisian3,4, ∼247 Ma). Here, we describe the geologically oldest sea-going reptile from the Southern Hemisphere - a nothosaur (basal sauropterygian5) from the Middle Triassic (Anisian, after ∼246 Ma6) of New Zealand. Time-scaled ancestral range estimations thus reveal an unexpected circum-Gondwanan high-paleolatitude (>60° S7) dispersal from a northern Tethyan origination center. This coincides with the adaptive diversification of sauropterygians after the end-Permian mass extinction8 and suggests that rapid globalization accompanied their initial radiation in the earliest Mesozoic.

Exceptional X-Ray contrast: Radiography imaging of a Middle Triassic mixosaurid from Svalbard.

The black shales of the Middle Triassic Botneheia Formation in Svalbard are known for their fossil richness with abundant ichthyosaur remains and beds of the bivalve Daonella. Vertebrate remains from the Muen Mountain on Edgeøya are shown to have exceptional X-ray contrast due to a combination of sulphide and sulphate permineralisation and pseudomorphing. Radiography imaging of a previously described specimen, PMO 219.250, revealed new and spectacular details such as more carpals, teeth, and skull sutures. Teeth and skull characters are taxonomically significant. supporting the referral of PMO 219.250 to Phalarodon and further suggesting an affinity to P. atavus. Three sulphur phases were identified, with the sulphide sphalerite (ZnS) being the highest temperature phase, followed by the sulphate baryte (BaSO4), and the sulphide pyrite (FeS2). Sulphate permineralisation is also seen in specimens from the Upper Jurassic on Svalbard. We suggest that sulphur-rich fluids have flowed and dissolved barium from the shales and deposited the sphalerite and baryte, and that this could be linked to the Cretaceous HALIP. The Jurassic specimens are only permineralised by baryte, while the Triassic specimens have also been permineralised, but mainly pseudomorphed by baryte with crystals of sphalerite. Lithology differences appear to have controlled the compaction of the Triassic specimens, while the Jurassic specimens have retained their three-dimensional shape due to the baryte emplacement relatively earlier in their depositional history. Although soft tissues are not preserved, the excellent X-ray contrast in the Middle Triassic specimens is reminiscent of pyritised fossil sites such as the Hunsrück Slate (Devonian), Beecher's Trilobite Bed (Ordovician), and the La Voulte-sur-Rhône marls (Jurassic).

Earliest Triassic ichthyosaur fossils push back oceanic reptile origins.

Reptiles first radiated into oceanic environments after the cataclysmic end-Permian mass extinction (EPME)1, 251.9 million years (Ma) ago. The geologically oldest fossils evincing this adaptive transition have been recovered from upper-Lower Triassic (lower Spathian) strata, ∼248.8 Ma2, and postdate a landmark turnover of amphibian-dominated to reptile-dominated marine ecosystems spanning the late Smithian crisis (LSC)3, ∼249.6 Ma4 -less than ∼2.3 Ma after the EPME. Here, we report ichthyopterygian (the group including 'fish-shaped' ichthyosaurians1) remains from the Arctic island of Spitsbergen that predate the LSC in later-middle to early-late Smithian5 deposits up to ∼250 Ma. Unexpectedly, however, their large size and spongy internal bone structure indicate a fully pelagic ichthyopterygian1,6. Given this unambiguous occurrence ∼2 Ma after the EPME, these pioneering seagoing tetrapods can now be feasibly recast as mass extinction survivors instead of ecological successors2,3 within the earliest Mesozoic marine predator communities.

A New Ophthalmosaurid (Ichthyosauria) from Svalbard, Norway, and Evolution of the Ichthyopterygian Pelvic Girdle.

In spite of a fossil record spanning over 150 million years, pelvic girdle evolution in Ichthyopterygia is poorly known. Here, we examine pelvic girdle size relationships using quantitative methods and new ophthalmosaurid material from the Slottsmøya Member Lagerstätte of Svalbard, Norway. One of these new specimens, which preserves the most complete ichthyosaur pelvic girdle from the Cretaceous, is described herein as a new taxon, Keilhauia nui gen. et sp. nov. It represents the most complete Berriasian ichthyosaur known and the youngest yet described from the Slottsmøya Member. It is diagnosed on the basis of two autapomorphies from the pelvic girdle, including an ilium that is anteroposteriorly expanded at its dorsal end and an ischiopubis that is shorter or subequal in length to the femur, as well as a unique character combination. The Slottsmøya Member Lagerstätte ichthyosaurs are significant in that they represent a diverse assemblage of ophthalmosaurids that existed immediately preceding and across the Jurassic-Cretaceous boundary. They also exhibit considerable variation in pelvic girdle morphology, and expand the known range in size variation of pelvic girdle elements in the clade.