Sinking of Four Species of Living Diatom Cells Directly Observed by a "Tumbled" Optical Microscope.

The study of the sinking phenomenon of diatom cells, which have a slightly larger specific gravity (~1.3) compared to that of water, is an important research topic for understanding photosynthetic efficiency. In this study, we successfully demonstrated the observation of the sinking behaviors of four different species of diatom using a homemade "tumbled" optical microscope. A homemade 1 mm3 microchamber was employed to decrease the effects of convection currents. In the microchamber, diatom cells were basically settled in a linear manner without floating, although some of the cells were rotated during their sinking. Sinking speeds of the four species of diatom cells, Nitzschia sp., Pheodactylum tricornutum, Navicula sp., and Odontella aurita, were 0.81 ± 5.56, 3.03 ± 10.17, 3.29 ± 7.39, and 11.22 ± 21.42 µm/s, respectively, based on the automatic tracking analysis of the centroids of each cell. Manual analysis of a vector between two longitudinal ends of the cells (two-point analysis) was effective for quantitatively characterizing the rotation phenomenon; therefore, angles and angular velocities of rotating cells were well determined as a function of time. The effects of the cell shapes on sinking velocity could be explained by simulation analysis using the modified Stokes' law proposed by Miklasz et al.

Single cell analysis of sinking diatoms studied using a homemade 'tumbled' optical microscope system.

Diatoms are one of the major photosynthetic planktons. Here, we studied movements of aqueous suspensions of diatoms using a home-made 'tumbled' optical microscope system. The usual inverted optical microscope was reoriented using a homemade microscope stand so that the vertical sample stage contacted the surface. To observe the intrinsic sinking phenomenon of individual Navicula sp. cells, which have slender bodies, a homemade microchamber (1 mm3) was employed. Most of the cells uniformly sunk with a velocity of 2 to 14 µm/s. Automatic and manual two points trajectory analyses were carried out. The manual analysis was able to assess the rotation of cells. The novel methods provide new information about cell movements in aqueous systems that could not be obtained using conventional methods.