Abstract

The hypotheses about the origin of the primitive amniotic tarsus are very speculative. Early studies argued that the origin of the astragalus, one of the largest proximal bones in the tarsus of basal amniotes, was produced by either the fusion of two, three, or even four of the original tarsal bones, the intermedium, the tibiale and the proximal centralia (c4 and c3), or that the intermedium alone transforms into the primitive astragalus. More recent studies have shown that the structure of the tarsus in Captorhinus supports the former hypothesis about a fusion of the intermedium, the tibiale, the proximal centrale (c4) and eventually c3, producing a purportedly multipartite structure of the amniotic astragalus, but the issue remained contentious. Very well preserved tarsi of the Early Permian aquatic amniote Mesosaurus tenuidens Gervais, 1864–1865, which represent the most complete ontogenetic succession known for a basal amniote (the other exceptional one is provided by the Late Permian diapsid Hovasaurus boulei Piveteau, 1926), suggest that there is more than one ossification center for the astragalus and that these fuse during late embryonic stages or maybe early after birth. A non-hatched Mesosaurus in an advanced stage of development shows that the tarsus is represented by a single bone, most probably the astragalus, which seems to be formed by the suturing of three bones, here interpreted as being the intermedium, the tibiale, probably already integrated to the c4 in an earlier stage of the development, and the c3. An amniote-like tarsal structure is observed in very basal Carboniferous and Permian tetrapods such as Proterogyrinus, Gephyrostegus, the diadectids Diadectes and Orobates, some microsaurs like Tuditanus and Pantylus and possibly Westlothiana, taxa that were all considered as true amniotes in their original descriptions. Therefore, the structure of the amniotic tarsus, including the configuration of the proximal series formed by the astragalus and the calcaneum, typically a pair of enlarged bones, could have been established well before the first recognized amniote walked on Earth. Accordingly, the tarsus of these taxa does not constitute specialized convergences that appeared in unrelated groups, they might be instead, part of a transformation series that involves taxa closely related to the early amniotes as some hypotheses have suggested.

Highlights

  • The origin of the astragalus and the calcaneum in the ankle of basal amniotes has been considered as an adaptation to terrestrial locomotion and a key innovation in the origin of Amniota (Romer, 1956)

  • We present a synoptic view of the evidence we found for homologizing the primitive amniotic astragalus to the intermedium plus possibly the tibiale and proximal centralia, and propose that the suturing of these elements occurred during the embryonic stage, producing a very specialized single bone in the hatchlings

  • The non-hatched Mesosaurus tenuidens found in the Early Permian of Uruguay is so exquisitely preserved that it allows us to describe the morphology of what we interpret to be a composite astragalus that is one millimeter in length! It possibly shows the precursors of the typical amniotic astragalus united by weak sutures (Fig. 9)

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Summary

Introduction

The origin of the astragalus and the calcaneum in the ankle of basal amniotes has been considered as an adaptation to terrestrial locomotion and a key innovation in the origin of Amniota (Romer, 1956). Taking into account the elements present in the tarsus of basal tetrapods, it is clear that there was a strong reduction in the number of bones that form the primitive amniotic tarsus. This reduction can be explained by the fusion or loss of some tarsal bones in the ancestral amniotes despite the homology of these elements not always is well established. Some authors supported the classic hypothesis of a unitary origin for the astragalus, from the intermedium (see Romer, 1956) or perhaps from the fusion of this bone to the tibiale (e.g., Holmgren, 1933; Gegenbaur, 1864 in Schaeffer, 1941). Recent reports of well-preserved tarsi from apparently young individuals of several captorhinid species (Kissel, Dilkes & Reisz, 2002; Berman & Henrici, 2003; O’Keefe et al, 2005; O’Keefe et al, 2006), which will be discussed later, demonstrate that the matter is still open

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