1981
DOI: 10.1007/bf00397110
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Improved fluorescent microscopy for measuring the standing stock of phytoplankton including fragile components

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Cited by 52 publications
(24 citation statements)
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“…Physiological condition was determined by the fluorescence of individual cells within the colonies. Phytoplankton lose their autofluorescence when in poor condition; reductions of 30 % immediately upon death and 75 % 24 h after death have been reported (Tsuji & Yanagita 1981). Healthy P. pouchetii populations normally form lobed colonies with individual cells showing medium-bright, red-orange autofluorescence, while cells from unhealthy colonies lose fluorescence and individual colonies become depleted of cells, the latter due either to cell death or to transformation to the motile stage (Verity et al 1988).…”
Section: Methodsmentioning
confidence: 99%
“…Physiological condition was determined by the fluorescence of individual cells within the colonies. Phytoplankton lose their autofluorescence when in poor condition; reductions of 30 % immediately upon death and 75 % 24 h after death have been reported (Tsuji & Yanagita 1981). Healthy P. pouchetii populations normally form lobed colonies with individual cells showing medium-bright, red-orange autofluorescence, while cells from unhealthy colonies lose fluorescence and individual colonies become depleted of cells, the latter due either to cell death or to transformation to the motile stage (Verity et al 1988).…”
Section: Methodsmentioning
confidence: 99%
“…Competition experiments were sampled approximately every three days. Samples were fixed with a paraformaldehyde-glutaraldehyde solution (Tsuji and Yanagita 1981). The population densities in these species mixtures were analyzed with the EurOPA flow cytometer (Dubelaar et al 1989, Jonker et al 1995.…”
Section: Sampling and Countingmentioning
confidence: 99%
“…Samples (1 ml) preserved with a mix of glutaraldehyde and formaldehyde (Tsuji and Yanagita 1981) were filtered onto a 0.02-m, 25-mm Whatman Anodisc filter and stained using a mixture of SYBR I and SYBR II green (Molecular Probes) fluorescent DNA and RNA markers, respectively (final dilution 4 ϫ 10 Ϫ3 v/v each). The filters were then mounted between a slide and cover slip using Aquapolymount (Polysciences).…”
Section: Methodsmentioning
confidence: 99%