AME 20:119-128 (1999)  -  doi:10.3354/ame020119

ABSTRACT: Fluorescently labeled tracers (FLT) are often used to estimate the loss rates of picoplankton to grazers. These tracers are commonly enumerated by epifluorescence microscopy, although flow cytometry is a viable alternative in the detection of FITC (fluorescein-5-isothiocyanate)- or DTAF (5-([4,6-dichlorotriazin-2-yl)amino]-fluorescein)-stained bacterial tracers. However, the bacterivory measured with FLT has hardly been applied to routine monitoring of oceanic waters, partly because of the time-consuming preparation of the tracers and other problems associated with the long-term incubations needed to generate detectable rates of tracer change. In addition, these long-term incubations make samples especially sensitive to the unwanted addition of nutrients carried over with the tracers. Here we present some experiments designed to ease the estimation of grazing rates on bacteria with this technique. Two bacterial strains and 2 fluorescent dyes were tested: Escherichia coli minicells (0.065 μm³) and Pseudomonas diminuta (0.064 μm³), stained with DTAF or with FITC. In addition, instead of the common use of pyrophosphate buffer during the staining protocol, the use of carbonate-bicarbonate buffer and cells scraped directly from solid media is suggested to avoid the problems associated with phosphorus enrichment of the sample that at times can occur in oligotrophic water samples. The FITC- or DTAF-stained tracers can be observed with either epifluorescence microscopy or flow cytometry. However, FITC- or DTAF-stained P. diminuta were more easily resolved with the flow cytometer than stained minicells. Flow cytometric detection of P. diminuta tracers, prepared in bicarbonate-buffer and stained with FITC, is a fast protocol for the estimation of the grazing loss rates of bacteria in oceanic environments.

KEY WORDS: Bacterial grazing rates · Flagellates · Flow cytometry · Pseudomonas diminuta