2006
DOI: 10.1002/cyto.a.20332
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Syringe pumped high speed flow cytometry of oceanic phytoplankton

Abstract: Background: Nanophytoplankton (2-20 lm) are less numerous than picophytoplankton (<2 lm) in the oceans but their biomass and production are comparable and sometimes higher. The accuracy of cytometry-based enumeration of phytoplankton ultimately depends on cell abundance and sample flow rate. Commercial flow cytometers in which sheath and core streams are driven by air pressure cannot produce sufficiently high, stable sample flow rate. The present study demonstrates the applicability of a syringe pump for flow … Show more

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Cited by 74 publications
(46 citation statements)
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“…Previous work has shown no loss of either prokaryotic or eukaryotic cells occurs upon fixation (Zubkov and Burkill, 2006). Synechococcus cells were counted unstained (Zubkov et al, 2000) while eukaryotic phytoplankton and Prochlorococcus were counted after staining with SYBR Green I (Sigma-Aldrich, 1:5000 dilution of the commercial stock; see Zubkov et al, 2000Zubkov et al, , 2007.…”
Section: Methodsmentioning
confidence: 99%
“…Previous work has shown no loss of either prokaryotic or eukaryotic cells occurs upon fixation (Zubkov and Burkill, 2006). Synechococcus cells were counted unstained (Zubkov et al, 2000) while eukaryotic phytoplankton and Prochlorococcus were counted after staining with SYBR Green I (Sigma-Aldrich, 1:5000 dilution of the commercial stock; see Zubkov et al, 2000Zubkov et al, , 2007.…”
Section: Methodsmentioning
confidence: 99%
“…Marie et al, 1997). An internal standard of 0.5 and 1.0 µm beads (Fluoresbrite microparticles, Polysciences), the concentration of which was determined by syringe pump flow cytometry (Zubkov and Burkill, 2006b), was added to each of the samples. Bacterioplankton groups were distinguished according to their DNA content and scatter properties.…”
Section: Bacterioplanktonmentioning
confidence: 99%
“…Yellow-green 0.5 and 1.0 mm reference beads (Fluoresbrite Microparticles, Polysciences, Warrington, PA, USA) were used in all analyses as an internal standard for both fluorescence and flow rates. The absolute concentration of beads in the stock solution was determined using syringe pump flow cytometry (Zubkov and Burkill, 2006).…”
Section: Sampling and Bacterioplankton Enumerationmentioning
confidence: 99%