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The ontogeny of the northwestern Atlantic batoid, Leucoraja ocellata, is described with special focus on the development of skate specific morphologies and the development of the fins. The results show that the sequence of events involving the early outgrowth of the paired fins and the initial development of the pharyngeal region is remarkably constant in skates, holocephalians, and sharks. However, differences exist in timing of the reshaping of the mandibular arch region, development of branchial filaments, median fins, denticles, and the order of branchial cleft formation. Despite the similarities of early events related to development of the branchial region and initial outgrowth of the fins, later stages are increasingly characterized by taxon-specific morphologies making a universal staging table for chondrichthyans less applicable. The staging table presented in this study represents an important resource for future studies on batoid embryology.
Anat Rec (Hoboken) 2008 Sep
PMID:Variability and conservation in late chondrichthyan development: ontogeny of the winter skate (Leucoraja ocellata). 1849 33

The serrated, or denticulated, ziphodont teeth of theropod dinosaurs display variability in their extent of denticulation. The functional model proposed here tests the hypothesis that denticles will not exist in areas that do not frequently contact the substrate. This area, defined as the "dead-space," is determined by the direction the tooth moves through the fleshy substrate. The extent of denticulation, as well as the dead-space dimensions, is measured from photographs of 235 isolated and in situ theropod teeth, to determine a meaningful relationship between the two variables. Both Euclidean and geometric morphometric methods are employed, and the data are expressed in bivariate and ordination plots. The model predicts the direction of tooth movement through the curvature of the tip/apex. Tooth position and taxon are considered. The results show that the mesial margin is usually partially denticulated, while the distal margin is usually totally denticulated. Curved teeth have large dead-spaces, and tend to be less denticulated mesially. Straighter teeth are more extensively denticulated, to the point where they became symmetrical. The mesial denticulation is determined by the dead-space, and dictated by the substrate contact. The dead-space almost always predicted less extensive denticulation; a consequence of the model's limitations. Tooth curvature increases with a more distal position, due to rotation based on the proximity to the hinge. Denticulation indicates that theropods used a distally oriented puncture to modify the substrate, similar to modern analogues. Although there is little taxonomic variation, Troodontidae show unique and extreme degrees of mesial denticulation.
Anat Rec (Hoboken) 2009 Sep
PMID:A functional explanation for denticulation in theropod dinosaur teeth. 1971 61

Metriorhynchidae was a peculiar but long-lived group of marine Mesozoic crocodylomorphs adapted to a pelagic lifestyle. Recent discoveries show that metriorhynchids evolved a wide range of craniodental morphotypes and inferred feeding strategies. One genus, Dakosaurus, is arguably the most aberrant marine crocodylomorph due to its large, robust, ziphodont teeth; very low tooth count; and brevirostrine/oreinirostral snout. We here report an additional unusual feature of Dakosaurus that is unique among marine crocodylomorphs: tightly fitting tooth-to-tooth occlusion, whose inference is supported by reception pits along the upper and lower tooth rows, indicative of vertically orientated crowns that were in close contact during occlusion, and three distinct types of dental wear. These include irregular spalled surfaces near the apex (probably caused by tooth-food contact), semi-circular wear near the base, and elongate surfaces extending along the mesial and distal margins of the teeth, obliterating the carinae (including the denticles). Scanning electron micrographs show that these latter surfaces are marked by parallel apicobasal striations, which in extant mammals reflect tooth-tooth contact. As such, we interpret the carinal wear facets in Dakosaurus as being formed by repeated tooth-tooth contact between the mesial and distal margins of the teeth of the upper and lower jaw. We posit that this increased the available shearing surface on their high crowns. Together, these wear patterns suggest that occlusion in Dakosaurus was specialized for cutting large and abrasive prey items into portions small enough to swallow, making it a prime example of an aquatic reptile with macrophagous feeding habits.
Anat Rec (Hoboken) 2012 Jul
PMID:Tooth-on-tooth interlocking occlusion suggests macrophagy in the mesozoic marine crocodylomorph dakosaurus. 2257 71

The four, evolutionarily independent, lineages of suspension feeding elasmobranchs have two types of branchial filters. The first is a robust, flattened filter pad akin to a colander (e.g., whale sharks, mantas and devil rays) while the second more closely resembles the comb-like gill raker structure found in bony fishes (e.g., basking and megamouth sharks). The structure and the presence of mucus on the filter elements will determine the mechanical function of the filter and subsequent particle transport. Using histology and scanning electron microscopy, we investigated the anatomy of the branchial filters in 12 of the 14 species of Chondrichthyian filter-feeding fishes. We hypothesized that mucus producing cells would be abundant along the filter epithelium and perform as a sticky mechanism to retain and transport particles; however, we found that only three species had mucus producing goblet cells. Two of these (Mobula kuhlii and Mobula tarapacana) also had branchial cilia, indicating sticky retention and transport. The remaining filter-feeding elasmobranchs did not have a sticky surface along the filter for particles to collect and instead must employ alternative mechanisms of filtration (e.g., direct sieving, inertial impaction or cross-flow). With the exception of basking sharks, the branchial filter is composed of a hyaline cartilage skeleton surrounded by a layer of highly organized connective tissue that may function as a support. Megamouth sharks and most of the mobulid rays have denticles along the surface of the filter, presumably to protect against damage from large particle impactions. Basking sharks have branchial filters that lack a cartilaginous core; instead they are composed entirely of smooth keratin.
Anat Rec (Hoboken) 2014 Apr
PMID:Comparison of the structure and composition of the branchial filters in suspension feeding elasmobranchs. 2444 16