Ophthalmosaurids were highly derived and the youngest clade of ichthyosaurs. Their evolutionary history comprises ~76 Myr (from the early Middle Jurassic to the final extinction of the group at the Cenomanian–Turonian boundary). Fossil records indicate that soon after they emerged they achieved a widespread geographical distribution. Analyses of disparity based on craniodental morphologies, and the co-occurrence of different bone histology and microstructure among the members of the group, indicate that ophthalmosaurids are not only taxonomically but also ecologically diverse. A region of the skull that is particularly complex among ophthalmosaurid taxa is the external nares and surrounding areas, but there have been few attempts to explore this topic. We describe a new ophthalmosaurid from the Late Jurassic of Patagonia (Argentina) in the genus Arthropterygius and analyse its phylogenetic relationships. A detailed exploration of the skull, using computed tomography, reveals the division of the external nares by means of a stout bony pillar. This condition was previously known only in some Cretaceous forms and, within a phylogenetic framework, its distribution among ophthalmosaurids indicates that this morphology was the result of convergent evolution. Based on available data on extant (and some extinct) forms, we explore putative soft structures involved in the narial region. We propose that the division of the external nares (complete or partly osseous) was related functionally to the separation of the air passage from the outlet of nasal salt glands in such a way that the salt glands could be evacuated underwater, while the air passage could be closed by a valvular system.
Morphological and physiological features indicate Metriorhynchidae as the only group of crocodylomorphs with a pelagic lifestyle. Some of these features have evolved convergently in several clades of tetrapods secondarily adapted to aquatic life. One striking feature of metriorhynchids as compared to other crocodylomorphs is the morphology of the pelvic region (i.e., ventrally deflected sacral ribs and reduced pelvic girdle), which increases significantly the depth of this region. This morphology, as a whole, resembles that of other viviparous Mesozoic marine reptiles not phylogenetically related to metriorhynchids. We tested two alternative hypotheses of reproductive strategies in this clade: oviparity vs. viviparity. Given the lack of direct evidence supporting one or the other, we explored the use of evidence that may disconfirm either of these hypotheses. Using this counter-inductive approach, we found no cases contradicting viviparity in metriorhynchids, except for their phylogenetic position as archosaurs. A survey of reproductive modes amongst amniotes depicts the evolutionary plasticity of the transition to viviparity, and a widespread occurrence among tetrapods secondarily adapted to a marine life. Assuming oviparity for metriorhynchids implies egg-laying out of the water. However, their postcranial morphology (i.e., features of fore and hind limbs, pelvic girdle, and tail) contradicts this possibility. In this context, we rejected oviparity for metriorhynchids.
The application of network methodology in anatomical structures offers new insights on the connectivity pattern of skull bones, skeletal elements and their muscles. Anatomical networks helped to improve our understanding of the water-to-land transition and how the pectoral fins were transformed into limbs via their modular disintegration. Here, we apply the same methodology to tetrapods secondarily adapted to the marine environment. We find that these animals achieved their return to the sea with four types of morphological changes, which can be grouped into two different main strategies. In all marine mammals and the majority of the reptiles, the fin is formed by the persistence of superficial and interdigital connective tissues, like a ‘baby mitten', whereas the underlying connectivity pattern of the bones does not influence the formation of the forefin. On the contrary, ichthyosaurs ‘zipped up' their fingers and transformed their digits into carpal-like elements, forming a homogeneous and better-integrated forefin. These strategies led these vertebrates into three different macroevolutionary paths exploring the possible spectrum of morphological adaptations.
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