From the middle Paleozoic to the end of Mesozoic, ammonoids represent one of the major constituents of macro-organisms that are preserved as fossils in the epicontinental seas. Their rich fossil records and remarkable diversification of shell forms in space and time indicate that ammonoids are one of the best examples for understanding relationships between evolution of marine biota and changes in paleoenvironment and/or paleoceanography. The biotic and abiotic components in the ancient ocean are, obviously, closely connected through the chemical cycles and energy flow in the ancient eco-system. Therefore, for understanding the cause and/or effect of diversity change or extinction events in the ancient earth-and eco-system, identifying ecological niche, such as habitat, food habit, life history strategy, etc., of ammonoid species is extremely important.The mode of life of ammonoids has hitherto been investigated based mainly on functional morphology of their shells, as well as synpaleoecological analyses of fossil assemblages. The previous approaches on the basis of functional morphology are roughly divided into three aspects; (1) buoyancy of the animal including both a shell and a supposed soft part, (2) swimming and mobility and (3) depth habitat.Many workers (Trueman 1941;Heptonstall 1970;Ebel 1983;Saunders and Swan 1984;Saunders and Shapiro 1986;Ebel 1992;Shigeta 1993; and others) calculated density of living ammonoids based on shell thickness, volume ratio between a phragmocone and a body chamber, and the estimated density of the hypothetized soft part. Although there are some ambiguities, such as accuracy of shell thickness calculations based on theoretical models, quantity of cameral liquid in the phragmocone and the supposed soft part density, most previous studies, excluding Ebel (1983Ebel ( , 1992 and Shigeta (1993), estimated that living ammonoids had a density