Adaptation of Bathynellacea (Crustacea,Syncarida) to Life in the Interstitial (“Zoea Theory”)

This study aims at demonstrating that the Bathynellacea arose by neoteny from a zoea-like ancestor (“Zoea Theory”). Bathynellacea basically have a larval morphology. Their post-embryonic development passes through phases which are directly comparable with some in the development of primitive Eucarida. These phases are called the parazoeal and bathynellid phase, and correspond to the protozoeal and zoeal phase of Penaeidea, respectively. Running initially parallel to that of Penaeidea, the development of the Bathynellacea breaks off precociously. They reach sexual maturity at a stage which, in the Penaeidea, is followed by metamorphosis. There are reasons to assume that the development of all Syncarida originally passed through a series of free-living larval stages and underwent metamorphosis. The bathynellaceans reach adulthood at a stage which corresponds to the last larval stage of their ancestor. The ecological path to interstitial life of the Bathynellacea and the bearing of the “Zoea Theory” upon views as to their phylogenetic position are discussed. The classical example of a group of crustaceans thought to have arisen by neoteny, the Cladocera, is critically examined and found to be in need of reevaluation.     

Histological study of karaurids,the oldest known (stem) urodeles

Little is known about the initial phases of lissamphibian history (before the Cretaceous), because their fossil record is quite scanty. Only the morphology of the earliest members has been investigated, although other sets of data, from bone microanatomy and histology, are known to yield valuable paleobiological information. In the present study, we provide the first histological and microanatomical data on the oldest known stem-urodeles, the karaurids, from the Middle Jurassic. Three humeri from the Upper Bathonian, Oxfordshire, referred to juvenile or subadult individuals of Marmorerpeton and to an unnamed caudate of undetermined (but obviously non-larval) ontogenetic stage, were sampled in order to shed new light on the habitat and ontogeny of these basal caudates. The great compactness of the three humeri suggests that these salamanders were aquatic. The presence of extensive amounts of calcified cartilage in the humeri greatly strengthens the case for the presence of neoteny in these taxa, a suggestion that had initially been made on the basis of a few morphological characters. This constitutes the oldest known occurrence of neoteny in lissamphibians. Finally, bone histology reveals that the growth of Marmorerpeton and the related unnamed caudate was fairly slow and cyclic, a characteristic of extant lissamphibians.     

Cephalic muscle development in the Australian lungfish,Neoceratodus forsteri

Lungfishes are the extant sister group of tetrapods. As such, they are important for the study of evolutionary processes involved in the water to land transition of vertebrates. The evolution of a true neck, that is, the complete separation of the pectoral girdle from the cranium, is one of the most intriguing morphological transitions known among vertebrates. Other salient changes involve new adaptations for terrestrial feeding, which involves both the cranium and its associated musculature. Historically, the cranium has been extensively investigated, but the development of the cranial muscles much less so. Here, we present a detailed study of cephalic muscle development in the Australian lungfish, Neoceratodus forsteri, which is considered to be the sister taxon to all other extant lungfishes. Neoceratodus shows several developmental patterns previously described in other taxa; the tendency of muscles to develop from anterior to posterior, from their region of origin toward insertion, and from lateral to ventral/medial (outside‐in), at least in the branchial arches. The m.protractor pectoralis appears to develop as an extension of the most posterior m.levatores arcuum branchialium, supporting the hypothesis that the m.cucullaris and its derivatives (protractor pectoralis, levatores arcuum branchialium) are branchial muscles. We present a new hypothesis regarding the homology of the ventral branchial arch muscles (subarcualis recti and obliqui, transversi ventrales) in lungfishes and amphibians. Moreover, the morphology and development of the cephalic muscles confirms that extant lungfishes are neotenic and have been strongly influenced via paedomorphosis during their evolutionary history.