TEM Study of the Radular Teeth of the Chiton Acanthopleura japonica
The radula chiton teeth, Acanthopleura japonica, were examined using transmission electron microscopy (TEM). After cutting into segments corresponding roughly to three developmental stages from the onset of tooth development, the middle and the fully matured stages, toluidine blue staining has given the posterior side three different color patterns, colorless, reddish-brown, and black colors, respectively. At the colorless stage, the microvilli attached along the surface of the tooth cusp appeared to be dissembled and convert into the lamellar structure in the tooth interior. At the reddish-brown stage, the electron density between fibrous layers increased. A complex of tiny clusters of grains appeared along the fibrous layers. They seemed to aggregate each other to become larger. At the black stage, multiple layers consisting of irregular-shaped and various size of iron minerals were formed. After treating with an aqua regia solution, organic substances have remained between iron minerals, suggesting the abrasion-resistant role at the posterior side of chiton teeth during feeding. In addition, these minerals were randomly arranged. The lattice intervals of the ion minerals varied at an approximate range from 4.8 to 10.2 Å. Also, we have confirmed clearly the lattice fringe of apatite crystal in the core region.
KeywordsChiton Transmission electron microscopy Iron minerals Apatite crystal
The lateral teeth of the radula exhibit a sequential series of tooth developments along with the production of iron biominerals from the organic stage to the fully mineralized stage. Regarding the iron biominerals in the radula teeth of the chiton, the teeth were composed of multilayers of iron oxide, predominately in the form of magnetite, but also in other forms of ferrihydrite and lepidocrocite (Lowenstam 1967). Therefore, many studies have focused mainly on these iron biominerals in the tooth cusp (Lowenstam 1967; Kim et al. 1986; James et al. 1986; van der Wal 1989; Martin et al. 2009; Han et al. 2011). The tooth cusps of posterior side are mainly reinforced by the mineralization of magnetite at the matured stage. Due to its hardness, TEM study conducted by making thin sections has not been available in particular for the fully matured chiton teeth so far. On the other hand, the presence of a calcium phosphate mineral in the tooth core region has been examined using various techniques for a considerable time (Lowenstam and Weiner 1985; Kim et al. 1986; Evans et al. 1992; Evans and Alvarez 1999; Lee et al. 2000). Although a study using electron microscopy has been tried to demonstrate the presence of apatite crystal (Evans et al. 1992), the precise structure of apatite crystal has not yet fully elucidated. In this study, we have conducted the present study to demonstrate the unique iron mineral deposits and verify the detailed structure of apatite crystal mineral using an electron microscope.
2.2 Materials and Methods
Samples of the chiton Acanthopleura japonica were collected at Hachijojima’s coastal area, Tokyo, Japan. Radulae were extracted from the chiton. After the removal of the soft tissue, radulae were cut into segments corresponding roughly to the three developmental stages of radula teeth from the onset of tooth development, the middle, and the fully matured stages, by using a razor blade. Then samples were subjected to examine using transmission electron microscope. They were fixed with 2% glutaraldehyde in 0.1 M cacodylate buffer at pH 7.4 for 1 h at 5 °C, post-fixed with 1% osmium tetroxide in the same buffer for 1 h at 5 °C, dehydrated by passage through a series of ascending ethanol concentrations, and then embedded in Araldite 502. Thick sections were stained with toluidine blue solution. Based on different color patterns at the posterior side of ralular teeth, these developmental stages tentatively called the initial stage with colorless, the middle stage with reddish-brown, and the fully matured stage with black color were examined. Thin sections were obtained with a Porter Blum MT2 ultra-microtome (SORVALL) equipped with a diamond knife. Sections were stained with saturated uranyl acetate and lead citrate, and some were left unstained. Also, some treated with an aqua regia solution were subjected to study. Then, they were examined under a JEM 100CX electron microscope (JEOL) at an accelerating voltage of 80 kV.
2.3 Results and Discussion
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