Turbo (Marmarostoma) matsuzakiensis Tomida and Kadota with an in situ operculum was found in limestone within the tuffaceous sandstone of the middle Miocene Yugashima Group, at Shikura, Shizuoka Prefecture, Japan. The presence of an operculum on T. (M.) matsuzakiensis Tomida and Kadota is confirmed and described in this paper, and demonstrates the autochthonous occurrence of the fossil.
Introduction
Recently, Tomida and Kadota (2012) described Turbo (Marmarostoma) matsuzakiensis from the Shikura Limestone, which is intercalated with the pale green, tuffaceous, fine-grained sandstone of the middle Miocene Yugashima Group, at Shikura, Matsuzaki-cho, Kamo-gun, Shizuoka Prefecture (Figures 1, 2). The Izu Peninsula is known to have drifted northward as an island on the Philippine Sea Plate, and was located in the tropical West Pacific Ocean around 15°N during the middle Miocene (Hirooka et al., 1985). Concerning the geological age of the Yugashima Group in this area, Koyama (1986), Okada et al. (1986) and Okada (1987) reported that the Sakurada Formation, the middle part of the Yugashima Group, can be assigned to the calcareous nannofossil zone CN4 (14.9–13.5 Ma) (Okada and Bukry, 1980).
The occurrence of a gastropod fossil with an in situ operculum is not so common, but there are some reports from geological formations all over the world. For example, the following records are from Paleozoic deposits: Gordon and Yochelson, 1982 (Carboniferous Naticopsis); Linsley et al., 1989 (Carboniferous Naticopsis); Guvanov and Yochelson, 1994 (Silurian Australonema); Horny and Peel, 1995 (Silurian Tophicola); Peel and Horny, 1996 (Devonian Carcassonnella); Rohr et al., 2008 (Silurian Australonema), whereas such records from Japan are less common than outside Japan: Iwasaki, 1980 (Cretaceous Pila); Kase and Maeda, 1980 (Cretaceous Hayamia); Noda and Kikuchi, 1980 (Miocene Phanerolepida); Matsuoka and Nakamura, 1981 (Pleistocene Cipangopaludina); Majima, 1984 (Neogene naticid); Majima and Fukuta, 1986. Majima and Fukuta (1986) reported 29 fossil shells of Naticidae with an in situ operculum from Japanese Neogene formations, and divided them into 5 types depending on the shell morphology and operculum position. All of the above-mentioned fossil gastropods from the Japanese formations were sandy or muddy bottom dwellers. In almost all cases the operculum is missing from the shell, because the shells were mostly transported far from their habitat. It is rarer to find a rocky shore gastropod with an in situ operculum than a sandy or muddy shore gastropod. A fossil of the genus Turbo with in situ operculum has been found in a Japanese formation for the first time.
The purpose of this paper is to describe two specimens of T. (M.) matsuzakiensis that still retain their operculum, and to discuss the habitat of this species from the view-point of paleoecology.
Systematics
Repository.—The materials used in this study are housed at the Nagoya University Museum (abbreviated as NUM).
Materials.—Two shells with an in situ operculum (NUM-Fa183 and NUM-Fa184) were examined.
Locality.—The specimens used for the description were obtained from the Shikura Limestone, which is intercalated with the pale green, tuffaceous, fine-grained sandstone of the middle part of the Yugashima Group, at Shikura (34°44′27″N; 138°47′18″E), Matsuzaki-cho, Kamo-gun, Shizuoka Prefecture (Figures 1, 2).
Family Turbinidae Rafinesque, 1815
Genus
Turbo
Linnaeus, 1758
Subgenus Marmarostoma Swainson, 1829
Turbo
(Marmarostoma
) matsuzakiensis
Tomida and Kadota, 2012
Figures 3–5
Turbo (Marmarostoma) matsuzakiensis Tomida and Kadota, 2012, p. 53, figs. 3–7; Tomida and Kadota, 2014, p. 73, figs. 4.6A, B, fig. 5.
Description.—Shell: see Tomida and Kadota, 2012, p. 53.
Operculum slightly ovate, strongly convex on outside and flat inside. Outside smooth; side around central part of inner lip vertical, smooth, and slightly curved in outline; side of outer lip somewhat curved and periphery not so thin. Inside flat and with volute consisting of 3 to 4 whorls.
Measurements.—Operculum 1: Maximum diameter 26.1 mm, minimum width 21.0+ mm, thickness 8.7 mm; shell 1: Maximum width 55.8 mm, minimum width 50.7 mm, height 64.7+ mm (NUM-Fa183); Operculum 2: Maximum diameter 38.5+ mm, thickness 9.6+ mm; shell 2: Maximum width 63.1 mm, minimum width 58.2 mm, height 89.5 mm (NUM-Fa184).
Remarks.—The operculum (NUM-Fa183) is situated a short distance (ca. 10–15 mm) from the shell aperture in a posterior direction, positioned on the inflated outer side in an anterior direction, and near the vertical style lying against the internal wall of the body whorl. The inner-lip side of this operculum is slightly opened at a distance of about 3 mm from the inner-lip side of the aperture, and the outer-lip side of the operculum is very close to the outer-lip side of the aperture. However, this operculum does not move along the horizontal axis (Figure 3B–F). The outer-lip side of the operculum was strongly adhered to the internal wall of the body whorl, because the calcite had recrystallized.
The other operculum (NUM-Fa184) is situated a short distance (ca. 10 mm) from the shell aperture in a posterior direction, positioned on the inflated outer side in an anterior direction, and near the vertical style lying against the internal wall of the body whorl. The inner-lip side of this operculum is slightly opened at a distance of about 3–4 mm from the inner-lip side of the aperture, and the lower-lip side of the operculum is also slightly opened at a distance of about 5–7 mm from the lower-lip side of the aperture. The upper-lip side of the operculum is close to the upper-lip side of the aperture. However, this operculum does not move along the horizontal axis (Figure 4C–E). These features were observed in a section of the aperture after being cut at the time of discovery. The surface of this operculum is difficult to observe due to the removal of the closely adhering matrix.
It is likely that when these turbinid gastropods had been deposited each had a closed-style operculum, which coincides with the type 1 of Majima and Fukuta (1986).
Comparisons.—Tomida and Kadota (2014) described one species of Turbo (Turbo) and three species of T. (Marmarostoma) including only one juvenile shell of T. (M.) matsuzakiensis and an isolated operculum of T. (M.) sp. from the Ena Limestone in Matsuzaki-cho, located about 3.5 km north of Shikura. Many fossil opercula were obtained from the locality, but they are badly preserved with eroded and polished surfaces. However the present in situ operculum from the Shikura Limestone is distinguishable from the operculum of T. (M.) sp. from the Ena Limestone in having a thicker and a more developed wall of the inner-lip side.
Vermeij and Williams (2007) mentioned that the opercula of turbinids in the Indo Pacific group are extremely thick, indicating that very thick opercula were already present in the Indo-Western Pacific in the Miocene, and discussed geographical patterns in turbinid opercular thickness. The present case from the Miocene Shikura Limestone corroborates their results well.
Discussion
The Shikura Limestone yields abundant Turbo (Marmarostoma) matsuzakiensis Tomida and Kadota (at present 23 specimens), accompanied by a few shallow-water molluscan species, e.g. Cerithium aff. nodulosum Bruguière, 1792 (3 specimens), Clypeomorus sp. (1 specimen), Cypraea sp. (1 specimen), Virgiconus sp. (2 specimens) and Chlamys sp. (2 specimens), and also by some other tropical elements such as the semi-autochthonous, large, limestone blocks of reef-building corals, large calcareous algae and a large calcareous foraminifer, Nephrolepidina japonica (Yabe, 1906). Judging from these fossils, the fauna of the Shikura Limestone is composed of tropical elements, and it seems that the molluscan species, e.g. Cerithium aff. nodulosum Bruguière was a sandy bottom dweller between the reef-building corals in the intertidal zone and the subtidal zone; Clypeomorus sp., Cypraea sp., Virgiconus sp. and Chlamys sp. are small-sized forms that dwelt on the shallow rocky bottom or directly on the reef-building coral in the intertidal zone. Moreover, there were very few molluscan fossils from the Shikura Limestone other than T. (M.) matsuzakiensis. Therefore, this fact shows the scarceness of large-sized mollusks in the reef-building coral colony. T. (M.) matsuzakiensis probably inhabited the edge of the coral reefs and rocky bottom, like T. (M.) argyrostomus Linnaeus, 1758. T. (M.) argyrostomus is an extant turban distributed in the adjacent seas of the Tanegashima-Yakushima and Ogasawara islands and southward, in the intertidal zone to 30 m water depth, on rocks (Sasaki, 2000).
T. (M.) matsuzakiensis includes individuals with heights ranging from 52.5 mm to 124.7 mm. For example, living T. (Batillus) cornutus [Lightfoot, 1786], including specimens as large as 130–150 mm in height, begin life as small juvenile shells inhabiting the intertidal zone to about 2 m water depth, but after 1–2 years as the mollusks (height more than 30± mm) grow older, they begin to transfer to deeper rocky sites of about 20 m water depth (Uno, 1962). No juvenile turbinid fossils have been found in the Shikura Limestone. Almost all the shells of T. (M.) matsuzakiensis have a well preserved top of the spire and aperture, and the blocks of the reef-building corals are large-sized. These facts indicate their autochthonous occurrence.
Acknowledgements
We are very grateful to Richard W. Jordan of the Department of Earth and Environmental Sciences, Faculty of Science, Yamagata University, who provided useful information and improved the English in this manuscript. We wish to express our thanks to Keisuke Inoue of the Department of Earth and Planetary Sciences, Faculty of Science, Nagoya University, for the preparation of the figures and photographs.