Estimating primary production rates from photosynthetic electron transport in estuarine microphytobenthos

By C. Barranguet, J. Kromkamp. 2000

159 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/40bab7a6d33d373ecdecf7df7549a54319c09fb7

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Citations in the corpus

Can chlorophyll fluorescence be used to estimate the rate of photosynthetic electron transport within microphytobenthic biofilms (2002, methodology): “Estimates of the photosynthetic electron transport rate (ETR) from fluorescence data have been compared with estimates of primary production, using 14Cradiotracers (Hartig et al. 1998, Wolfstein & Hartig 1998, Barranguet & Kromkamp 2000), and O2 evolution (Flameling & Kromkamp 1998).”
Patterns in microphytobenthic primary productivity: Species‐specific variation in migratory rhythms and photosynthetic efficiency in mixed‐species biofilms (2005, methodology): “The appropriate methodology for measuring microphytobenthic primary productivity is still debated (Underwood and Kromkamp 1999; Barranguet and Kromkamp 2000; Perkins et al. 2002).”
Influence of Corophium volutator and Hydrobia ulvae on intertidal benthic diatom assemblages under different nutrient and temperature regimes (2002, background): “Environmental variables considered in the analysis were: macrofaunal presence or absence; chl a; F015; temperature; salinity; sediment carbohydrate concentration (data not shown); final PO4, NO3, 50 Hagerthey et al.: Grazing, nutrient and temperature impacts on microphytobenthos NO2, NH4; and molar ”
Responses of microphytobenthos to light: primary production and carbohydrate allocation over an emersion period (2001, background): “ETR once Ek has been exceeded (Barranguet & Kromkamp 2000).”
Light response curve methodology and possible implications in the application of chlorophyll fluorescence to benthic diatoms (2006, methodology): “…productivity 64 using different methodologies, principally carbon uptake (radio-labeled 14 C), electron 65 transport rate (Chl a fluorescence) and oxygen evolution (oxygen electrodes) 66 (Flameling & Kromkamp 1998, Hartig et al. 1998, Barranguet and Kromkamp 2000, 67 Perkins et al. 2001, 2002).”
Short-term variability in the photosynthetic activity of microphytobenthos as detected by measuring rapid light curves using variable fluorescence (2005, background): “Despite the possible discrepancies between photosynthetic rates and fluorescence measurements (Hartig et al. 1998; Barranguet and Kromkamp 2000; Glud et al. 2002 ;S eroˆ dio 2003), the results obtained suggest that microphytobenthos cells may behave physiologically as photoacclimated to relatively”
The importance of fine-scale, vertical profiles in characterising nematode community structure (2003, background): “…and detailed background information on pigment distributions (Barranguet et al., 1997; Lucas & Holligan, 1999), microphytobenthos production (Barranguet & Kromkamp, 2000; Barranguet,Kromkamp,&Peene, 1998), photosynthetic activity (Kromkamp et al., 1998), microphytobenthos resuspension…”
Photosynthetic performance of surface-associated algae below sea ice as measured with a pulse amplitude-modulated (PAM) fluorometer and O2 microsensors (2001, methodology): “In any case, a prerequisite for more quantitative use of active fluorescence techniques for in situ studies in aquatic ecology is a careful and detailed intercalibration with oxygen exchange or 14C-based techniques (e.g. Hartig et al. 1998, Barranguet & Kromkamp 2000).”
Studying undisturbed autotrophic biofilms: still a technical challenge (2004, methodology): “In algal biofilms, pulse amplitude modulation (PAM) fluorimetry allows the measurement of algal photosynthetic activity, maximum quantum yield and algal biomass on undisturbed biofilm samples (Barranguet & Kromkamp 2000).”