1980
DOI: 10.1007/bf02988134
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Über den Kieferapparat der Lytoceratacea (Ammonoidea)

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Cited by 28 publications
(20 citation statements)
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“…10.5d; Phyllopachyceras: Tanabe and Landman 2002;Tanabe et al 2013) and Lytoceratina ( Tetragonites, Gaudryceras, Aanagaudryceras; F ig. 10.5e, 10.7a, b; Table 10.1; Tanabe et al 1980aTanabe et al , 2012Lehmann et al 1980;Kanie 1982;Tanabe and Landman 2002). In the two phylloceratids, the lower jaw is slightly larger than the upper jaw (Table 10.2).…”
Section: Rhynchaptychus Typementioning
confidence: 95%
See 1 more Smart Citation
“…10.5d; Phyllopachyceras: Tanabe and Landman 2002;Tanabe et al 2013) and Lytoceratina ( Tetragonites, Gaudryceras, Aanagaudryceras; F ig. 10.5e, 10.7a, b; Table 10.1; Tanabe et al 1980aTanabe et al , 2012Lehmann et al 1980;Kanie 1982;Tanabe and Landman 2002). In the two phylloceratids, the lower jaw is slightly larger than the upper jaw (Table 10.2).…”
Section: Rhynchaptychus Typementioning
confidence: 95%
“…10.9 and 10.12). The rhynchaptychus-type jaw apparatuses are known from the Late Cretaceous Phylloceratina (Tanabe and Landman 2002;Tanabe et al 2013) and Lytoceratina (Tanabe et al 1980aKanie 1982;Lehmann et al 1980;Tanabe and Landman 2002). In addition, wholly chitinous lower jaws of the Early Jurassic Phylloceras and Lytoceras were described as anaptychi (Schmidt 1928;Hauff 1953;Lehmann 1990).…”
Section: Taxonomic Evaluation Of Jaw Morphologymentioning
confidence: 99%
“…Westermann (1996) noted that besides the micro and mesophagy documented by crop/stomach contents, macrophagy and even duraphag ous strategies might have also been present in ammonoids (Schindewolf 1958;Lehmann et al 1980;Tanabe 1983;Nesis 1986;Tanabe and Fukuda 1987;Lehmann and Kulicki 1990;Hewitt 1993;Seilacher 1993;Keupp 2007). Westermann (1996) suggested that most ammonoids belonged to the pelagic food-web.…”
Section: Trophic Levelmentioning
confidence: 96%
“…Nonetheless, the implosion depth of a Nautilus shell does not represent an actual depth limit of living animals. Direct observations using a remote camera and capture records using baited traps have demonstrated that the optimal habitat depth of Nautilus ranges from 150 to 300 m in Palau and from 300 to 500 m in Fiji (Saunders 1984;Hayasaka et al 1987), whereas the shell implosion depth of Nautilus is about 800 m (Kanie et al 1980). Although these analyses in functional morphology provided valuable suggestions and limitations for considering ammonoid ecology, reasonable and unanswered questions remain for future discussion.…”
Section: Introductionmentioning
confidence: 94%
“…Many problems of dietary and feeding habits for the diversely shaped buccal organs remain essentially unsolved, even for most extant cephalopods (Nesis, 1986(Nesis, , 1987Lehmann, 1988). Of particular interest are the aptychus-type mandibles (including anaptychi) present in many but by no means all Mesozoic ammonoids, and the rhynchaptychus-type mandibles of the Lytoceratina (Lehmann et al, 1980). A consensus appears to be that, among the former, the uncalcified anaptychi functioned mainly as feeding organs, i.e., as lower mandibles or, perhaps, an elastic "pump" during suction feeding (Seilacher, 1993); the thickly calcified aptychi (Lamellaptychus, Laevaptychus, Punctaptychus) functioned primarily as opercula (Schindewolf, 1958; Lehmann and Kulicki, 1990;Seilacher, 1993).…”
Section: Buccal Organsmentioning
confidence: 99%