1993
DOI: 10.1111/j.1463-6395.1993.tb01217.x
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Development of the Snout of the Australian Lungfish Neoceratodus forsteri (Krefft, 1870), with Special Reference to Cranial Nerves

Abstract: The anatomy and embryology of the dipnoan snout and olfactory organ play a major role in the discussion about the phylogenetic position of Dipnoi and the question of ancestry of Tetrapoda. This is primarily due to the fact that an internal nostril is regarded as an important preadaptive organ of the ancestors of tetrapods. Two conflicting scenarios of phylogenetic change were proposed in favour of different hypotheses of relationship. One emphasizes the similarities between Dipnoi and Chondrichthyes concerning… Show more

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Cited by 19 publications
(18 citation statements)
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“…The formation of the nasal cavity and the anterior (incurrent) and posterior (excurrent) nostrils from an original single pit as described in this study, is considered the phylogenetically primitive (plesiomorphic) type among actinopterygians (Bertmar 1969;Zeiske et al1992). It closely resembles the formation of the naso-buccal pits and ventilatory openings of the olfactory organ in Dipnoi (Bertmar 1965;Bartsch 1993), and the incomplete separation of incurrent and excurrent opening in sharks (Berliner 1902). This type of formation has also been described for sturgeons (Devitsina and Kazhlayev 1993a), paddle fish Polyodon spathula (Ballard and Needham 1964;Bemis and Grande 1992) and the bowfin Amia calva (Dean 1897) as well as for many teleosts (e.g.…”
Section: Formation Of the Olfactory Organmentioning
confidence: 85%
“…The formation of the nasal cavity and the anterior (incurrent) and posterior (excurrent) nostrils from an original single pit as described in this study, is considered the phylogenetically primitive (plesiomorphic) type among actinopterygians (Bertmar 1969;Zeiske et al1992). It closely resembles the formation of the naso-buccal pits and ventilatory openings of the olfactory organ in Dipnoi (Bertmar 1965;Bartsch 1993), and the incomplete separation of incurrent and excurrent opening in sharks (Berliner 1902). This type of formation has also been described for sturgeons (Devitsina and Kazhlayev 1993a), paddle fish Polyodon spathula (Ballard and Needham 1964;Bemis and Grande 1992) and the bowfin Amia calva (Dean 1897) as well as for many teleosts (e.g.…”
Section: Formation Of the Olfactory Organmentioning
confidence: 85%
“…Finally, it is worth noting that, although no other amphibians have a larval olfactory epithelium with ridges of respiratory epithelium separating troughs of sensory epithelium like that of larval salamanders, similar structures have been described in early larval stages of lungfishes (Bartsch, 1993). In later stages, this arrangement persists in the "receptor grooves" on the surface of the primary gill lamellae (Derivot, 1984).…”
Section: General Morphology Of the Nasal Cavitiesmentioning
confidence: 93%
“…The development of the head, early events in particular, in the Australian lungfish are very poorly known. Only the later stages of development and the larval anatomy have been the subject of recent, thorough study ( Bartsch 1993, 1994; Kemp 1999). In the most recent study of neural crest development in the Australian lungfish, Kemp (1995) suggests that “In embryos of … the dipnoi, the cells of the neural crest may not form a part of the mesenchyme from which the dental and skeletal structures develop.” If true, this is very different from what would be expected and it would force us to develop reasonable explanations for why the Australian lungfish deviates so dramatically from other vertebrates in the development of its head.…”
Section: Introductionmentioning
confidence: 99%