IR Home
AME
Home
Editors
Forthcoming
Information
Subscribe
Journals
Home
MEPS
AME
CR
DAO
ESEP
ESR
Search
Subscribe
Book Series
EE Books
Top Books
ESEP Books
Order
EEIU Brochures
(pdf format)
Discussion Forums
Home
Research
IR Research
Institutions
International Ecology Institute
Eco-Ethics International Union
Foundation
Otto Kinne Foundation
![](../../../../images/pixel.gif) | ![](../../../../images/pixel.gif) |
AME 34:263-277 (2004)
|
Abstract
|
![](../../../../images/hline.gif)
Counting heterotrophic nanoplanktonic protists in cultures and aquatic communities by flow cytometry
Julie M. Rose1,*, David A. Caron1, Michael E. Sieracki2, Nicole Poulton2
1Department of Biological Sciences, University of Southern California, 3616 Trousdale Parkway, AHF 301, Los Angeles, California 90089-0371, USA
2Bigelow Laboratory for Ocean Sciences, PO Box 475, 180 McKown Point Road, West Boothbay Harbor, Maine 04575, USA
*Email: jrose@usc.edu
![](../../../../images/hline.gif)
ABSTRACT: The food vacuole stain LysoTracker Green® was used to enumerate heterotrophic protists on a standard model flow cytometer. Appropriate stain concentration and staining time were determined using cultures of protists. Stained
heterotrophic protists consistently formed distinct populations within cytograms of green fluorescence versus forward scatter. Cytometric counts of cultured species were compared to direct counts using light microscopy at cell abundances ranging from
103 to 106 cells ml-1. A regression of these data was highly significant and yielded a slope of 0.95. Stained populations were accurately counted during lag, exponential and early stationary growth phases. Growth rates
calculated from cytometric counts were not statistically different from those based on microscopy. The method was applied to 26 natural plankton samples, and general region definitions on the cytograms were established that identified heterotrophic
protistan assemblages. A regression of cytometric counts versus direct counts yielded a slope of 1.16. LysoTracker Green® can only be used with live samples because preservation destroys membrane potential, resulting in loss of fluorescence.
However, the flow cytometric method employing LysoTracker Green® is highly applicable for monitoring the growth of many heterotrophic protists in cultures and has the potential to be extremely useful for field samples, providing comparable
counts to microscopical methods while allowing much faster sample processing.
KEY WORDS: Heterotrophic protists · Flow cytometry · Nanoplankton · Fluorescent staining
Full text in pdf format
![](../../../../images/hline.gif)
Published in AME Vol.
34, No. 3
(2004) on March 9
Print ISSN: 0948-3055; Online ISSN: 1616-1564.
Copyright © Inter-Research, Oldendorf/Luhe, 2004
|