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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 159 (1979), S. 393-425 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Branchial food traps are regions of specialized secretory tissue in the tadpole pharynx, where suspended food particles are trapped in mucus.Light and scanning electron microscopy were used to study branchial food traps from larvae of ten anuran families (36 species). Most anuran larvae from “advanced” (suborder Neobatrachia) families (e.g., Hylidae, Ranidae, Bufonidae) have distinct secretory pits at the posterior margins of the branchial food traps and secretory ridges elsewhere on these surfaces. The apices of columnar PAS-positive, secretory cells are exposed on the floors of the secretory pits or in rows at the tops of the secretory ridges (secretory zone).Tadpoles from most “archaic” (suborder Archaeobatrachia) families (Ascaphidae, Discoglossidae and Pelobatidae) either lack secretory pits, or have them poorly defined. They also lack secretory ridges but have columnar, mucus-secreting cells whose apices are exposed in a seemingly random fashion in the branchial food traps. Rhinophrynus (Archaeobatrachia: Rhinophrynidae) has secretory ridges, but the apices of secretory cells are not arranged in rows at the tops of the ridges; instead they erupt singly or in small clusters on the epithelial surface, in a pattern similar to that in Ascaphus, the discoglossids and the pelobatids. It is proposed that the generalized condition for the branchial food trap mucosa is one where the apices of secretory cells are exposed haphazardly on a flat epithelium and the derived condition is one where the surface is organized into ridges. The morphology of the branchial food traps in Rhinophrynus suggests that, phylogenetically, ridges preceded the coalescing of secretory cell apices into distinct rows.Pipidae and Microhylidae have unique patterns in the gross and microanatomy of their branchial food traps specific to their families.Branchial food trap morphology relates to diets of tadpoles as well as to taxonomy. Obligate macrophagous (e.g., carnivorous) tadpoles, irrespective of family, tend to have reduced branchial food traps, regularly lack secretory ridges and, in extreme cases, lack columnar mucus-secreting cells. Obligate microphagous forms (midwater suspension feeding of Xenopus, microhylids and Agalychnis), have straight parallel secretory ridges with narrow secretory zones and shallow troughs between the ridges.Secretory ridges may help to form mucus strands in which food particles are trapped, but they are not essential for planktonic entrapment. The hydrodynamic implications of the various topographic patterns remain unclear.
    Additional Material: 30 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 182 (1984), S. 1-37 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Among egg-brooding hylid frogs there is much interspecific variation in the degree of development of the young at hatching. In certain species of Gastrotheca the eggs hatch into free-living tadpoles, whereas in others (and in the genera Amphignathodon, Cryptobatrachus, Stefania and Hemiphractus) the eggs hatch directly into frogs. We examined the oral anatomy of tadpoles and embryos of 22 species of egg-brooding hylids in order to determine the morphological differences between free-living larvae and embryos of species having direct development. All free-living Gastrotheca larvae are morphologically similar and have a large array of oral structures directly associated with a suspension feeding way of life. Among those egg-brooding hylids without free-living larvae there is a complete gradation from those with all of the free-living tadpole oral structures to those with none. Different lineages retain different vestiges of free-living larval morphology, suggesting that direct development has evolved multiple times among these frogs. All of the morphological patterns in the direct-developing embryos can be accounted for by simple truncation or acceleration of the normal tadpole developmental program. We explore the possibility that certain Gastrotheca species with tadpoles may have evolved from species that lack larval stages. The development of oral structures in egg-brooding hylids provides insight into the phylogenetic significance of these charactes in other groups of anurans. Most significantly they reinforce the idea that microhylids evolved from ranoidlike ancestors.
    Additional Material: 31 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 216 (1993), S. 141-159 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Aortic valve morphology was examined in 32 species of snakes representing 28 genera and 11 families and a diversity of habitat preferences. The results largely agree with previous studies but include some previously undescribed features, such as the cranial displacement of the cusps in the left aorta in some species and the structure of the opposing cusps of the interaortic foramen. Few features of the aortic valves are uniform among species. The pattern of morphological variation does not correlate with simple habitat preference (e.g., terrestrial, arboreal); however, some of the variation, particularly in the valves themselves, correlates with taxonomic relationships. We suggest that the presence of an interaortic foramen, with its associated valve, could result in an interaortic shunt of blood that potentially alters hemodynamics and flow patterns in the systemic circulation of snakes. © 1993 Wiley-Liss, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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