High Diversity, Low Disparity and Small Body Size in Plesiosaurs (Reptilia, Sauropterygia) from the Triassic–Jurassic Boundary

Invasion of the open ocean by tetrapods represents a major evolutionary transition that occurred independently in cetaceans, mosasauroids, chelonioids (sea turtles), ichthyosaurs and plesiosaurs. Plesiosaurian reptiles invaded pelagic ocean environments immediately following the Late Triassic extinctions. This diversification is recorded by three intensively-sampled European fossil faunas, spanning 20 million years (Ma). These provide an unparalleled opportunity to document changes in key macroevolutionary parameters associated with secondary adaptation to pelagic life in tetrapods. A comprehensive assessment focuses on the oldest fauna, from the Blue Lias Formation of Street, and nearby localities, in Somerset, UK (Earliest Jurassic: 200 Ma), identifying three new species representing two small-bodied rhomaleosaurids (Stratesaurus taylori gen et sp. nov.; Avalonnectes arturi gen. et sp. nov) and the most basal plesiosauroid, Eoplesiosaurus antiquior gen. et sp. nov. The initial radiation of plesiosaurs was characterised by high, but short-lived, diversity of an archaic clade, Rhomaleosauridae. Representatives of this initial radiation were replaced by derived, neoplesiosaurian plesiosaurs at small-medium body sizes during a more gradual accumulation of morphological disparity. This gradualistic modality suggests that adaptive radiations within tetrapod subclades are not always characterised by the initially high levels of disparity observed in the Paleozoic origins of major metazoan body plans, or in the origin of tetrapods. High rhomaleosaurid diversity immediately following the Triassic-Jurassic boundary supports the gradual model of Late Triassic extinctions, mostly predating the boundary itself. Increase in both maximum and minimum body length early in plesiosaurian history suggests a driven evolutionary trend. However, Maximum-likelihood models suggest only passive expansion into higher body size categories

Environmental Control on Biotic Development in Siberia (Verkhoyansk Region) and Neighbouring Areas During Permian-Triassic Large Igneous Province Activity

We propose an updated ammonoid zonation for the Permian-Triassic boundary succession (the lower Nekuchan Formation) in the Verkhoyansk region of Siberia: (1) Otoceras concavum zone (uppermost Changhsingian); (2) Otoceras boreale zone (lowermost Induan); (3) Tompophiceras morpheous zone (lower Induan); and (4) Wordieoceras decipiens zone (lower Induan). The Tompophiceras pascoei zone, previously defined between the Otoceras boreale and Tompophiceras morpheous zones, is removed in our scheme. Instead of this the Tompophiceras pascoei epibole zone is proposed for the lower part of the Tompophiceras morpheous zone. New and previously published nitrogen isotope records are interpreted as responses to climatic fluctuations in the middle to higher palaeolatitudes of Northeastern Asia and these suggest a relatively cool climatic regime for the Boreal Superrealm; however the trend towards warming across the Permian-Triassic boundary transition is also seen. The evolutionary development and geographical differentiation of otoceratid ammonoids and associated groups are considered. It is likely that the Boreal Superrealm was their main refugium, where otocerid, dzhulfitid and some other ammonoids survived the major biotic crisis at the end of the Permian. The similarity of ontogenetic development of suture lines of Otoceras woodwardi Griesbach and O. boreale Spath gives some grounds for suggesting a monophyletic origin of the genus Otoceras, having bipolar distribution

Ecological signature of the end-Triassic biotic crisis: what do bivalves have to say?

In order to understand the causes underlying the Triassic-Jurassic (T/J) mass extinction, we tested different bivalve features for extinction selectivity, i.e. shell mineralogy, age at the Rhaetian and three main autoecologic traits (feeding mechanism, tiering and motility/attachment). Also, diversity and turnover rates throughout the Triassic and the Early Jurassic were analysed in detail. The dataset employed for this analysis was a precise database at genus level including data from Induan to Sinemurian times. Results point to a true mass extinction for bivalves around the T/J boundary. This extinction was not ageselective at the boundary. Certain analyses suggested that shell mineralogy was a character significantly increasing survival odds, but this relationship seems to reflect selectivity on autoecologic traits. There was no difference in extinction proportions between both feeding types (i.e. deposit feeders and filter feeders); among the other traits, deep burrowers, epifaunal-motile and endobyssate forms seem to have been favoured, while shallow burrowers (and probably reclined forms) were more heavily affected. This pattern suggests an environmental stress at the boundary with some particular issues affecting the different life modes. Models linking magmatism in the Central Atlantic Magmatic Province with the end- Triassic mass extinction are a plausible scenario for this kind of perturbation

Ammonoid Intraspecific Variability

Because ammonoids have never been observed swimming, there is no alternative to seeking indirect indications of the locomotory abilities of ammonoids. This approach is based on actualistic comparisons with the closest relatives of ammonoids, the Coleoidea and the Nautilida, and on the geometrical and physical properties of the shell. Anatomical comparison yields information on the locomotor muscular systems and organs as well as possible modes of propulsion while the shape and physics of ammonoid shells provide information on buoyancy, shell orientation, drag, added mass, cost of transportation and thus on limits of acceleration and swimming speed. On these grounds, we conclude that ammonoid swimming is comparable to that of Recent nautilids and sepiids in terms of speed and energy consumption, although some ammonoids might have been slower swimmers than nautilids