Abstract

Excitation–emission fluorescence matrices of phytoplankton communities were simulated from laboratory-grown algae and cyanobacteria cultures, to define the optical configurations of theoretical fluorometers that either minimize or maximize the representation of these phytoplankton groups in community variable fluorescence measurements. Excitation sources that match the photosystem II (PSII) action spectrum of cyanobacteria do not necessarily lead to equal representation of cyanobacteria in community fluorescence. In communities with an equal share of algae and cyanobacteria, inducible PSII fluorescence in algae can be retrieved from community fluorescence under blue excitation (450–470 nm) with high accuracy (R 2 = 1.00). The highest correlation between community and cyanobacterial variable fluorescence is obtained under orange-red excitation in the 590–650 nm range (R 2 = 0.54). Gaussian band decomposition reveals that in the presence of cyanobacteria, the emission detection slit must be narrow (up to 10 nm) and centred on PSII chlorophyll-a emission (~683 nm) to avoid severe dampening of the signal by weakly variable phycobilisomal fluorescence and non-variable photosystem I fluorescence. When these optimizations of the optical configuration of the fluorometer are followed, both cyanobacterial and algal cultures in nutrient replete exponential growth exhibit values of the maximum quantum yield of charge separation in PSII in the range of 0.65–0.7.

Highlights

  • Differences in pigmentation are used to discriminate taxonomic phytoplankton groups in applications ranging from microscopy to remote sensing of water colour

  • The distinct absorption and fluorescence properties of cyanobacteria caused by the prominent role of phycobilipigments in photosynthetic light harvesting are already used to complement traditional observation methods in environmental monitoring (Lee et al 1994; Izydorczyk et al 2005; Seppalaet al. 2007)

  • Variable fluorescence measurements are increasingly included in these monitoring efforts, to reveal spatiotemporal trends in photosynthetic capacity or even photosynthetic activity of the phytoplankton

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Summary

Introduction

Differences in pigmentation are used to discriminate taxonomic phytoplankton groups in applications ranging from microscopy to remote sensing of water colour. Phycobilipigments extend the absorption of light to the green-orange part of the visible spectrum that is left unused by the algal groups. This spectral domain overlaps with the deepest penetration of solar irradiance in inland and coastal waters where turbidity and/or the concentration of coloured dissolved organic matter is high, yielding an advantage in light-harvesting at Photosynth Res (2012) 112:13–30 depth to phycobilin-containing species (Pick 1991; Stomp et al 2007). Owing to the differences in pigmentation between the major phytoplankton groups, absorption and fluorescence techniques can be used to interpret biomass at the community and sub-community level (Yentsch and Yentsch 1979; Kolbowski and Schreiber 1995; Beutler et al 2002; Millie et al 2002; Beutler et al 2003; Seppalaand Olli 2008). The distribution of Chla between photosystems I and II (PSI, PSII) is fundamentally different in these phytoplankton groups (Johnsen and Sakshaug 1996, 2007), and requires consideration in all aspects of phytoplankton community fluorescence measurements

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