David Caron WHOIMethods for nanoplankton counts
Assemblages of phototrophic (pnp) and heterotrophic (hnp) nanoplankton were preserved in a final concentration of 1% formalin and stored at 4 degrees C. Samples were prepared for enumeration by epifluoresence microscopy within 24 hrs of preservation by staining with DAPI at a final concentration of 25 ug/ml (Caron, 1983; Sherr et al, 1993). Phototrophic (chloroplast-bearing) nanoplankton were distinguished from heterotrophs by the autofluoresence of chlorophyll a. Biovolumes were estimated by calculating the volume of an appropriate geometric shape (usually a sphere) from samples at 4 representative depths and then extrapolated through the water column. References Caron, D.A. (1983) Technique for enumeration of heterotrophic and phototrophic nanoplakton, using epifluoresence microscopy, and comparison with other procedures. Applied and Enviromental Microbiology, 46, 491-498. Sherr, E.B., D.A. Caron and B.F. Sherr (1993) Staining of heterotrophic protists for visualization via epifluoresence microscopy. In: Handbook of methods in aquatic microbial ecology, Kemp, P., J. Cole, B. Sherr and E. Sherr, eds. Lewis Publishers, Boca Raton, pp. 213-227.