Evaluation of biophysical and optical determinations of light absorption by photosystem II in phytoplankton
By David John Suggett, Hugh L. MacIntyre, R. Geider. 2004
209 citations recorded by the source corpus.
Subfields: Molecular Biology, Oceanography, Renewable Energy, Sustainability and the Environment
View Paper: https://www.semanticscholar.org/paper/b9da7ca0cfe1e3df59ab1839e75e55d90bb2b46a
How researchers see this paper
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In Molecular Biology
- David John Suggett
- R. Geider
- CM Moore
- Hugh L. MacIntyre
- Mark E. Warner
- Anna Hickman
- S. Hennige
- Geir Johnsen
In Oceanography
- David John Suggett
- R. Geider
- CM Moore
- Hugh L. MacIntyre
- Mark E. Warner
- Anna Hickman
- S. Hennige
- T. Kana
In Renewable Energy, Sustainability and the Environment
- David John Suggett
- R. Geider
- CM Moore
- Mark E. Warner
- Anna Hickman
- Hugh L. MacIntyre
- Geir Johnsen
- T. Kana
Citations in the corpus
- Taxonomic Discrimination of Phytoplankton by Spectral Fluorescence (2010, methodology): “These carotenoids absorb light but do not contribute to the photosynthetic cross-section and account for much of the difference between absorption and PSII fluorescence excitation spectra (see Lutz et al. 2001; Suggett et al. 2004).”
- Photobiology of Symbiodinium revisited: bio-physical and bio-optical signatures (2009, methodology): “Emission was measured at 730 nm with excitation at 1 nm intervals between 400 and 715 nm to yield a PSII-specific fluorescence excitation spectrum (termed F730, Suggett et al. 2004, 2007).”
- Iron‐light interactions differ in Southern Ocean phytoplankton (2012, result): “So far as we are aware, the phenotypic plasticity in sPSII that we observed for P. antarctica is unprecedented, and compares with the at most 1.5-fold change observed in other phytoplankton species over a comparable irradiance range (Kolber et al. 1988; Suggett et al. 2004).”
- PSII photoinhibition and photorepair in Symbiodinium (Pyrrhophyta) differs between thermally tolerant and sensitive phylotypes (2010, methodology): “Measurements were carried out at t0 and t0+ 2h (light-response experiments) after 35 to 45 min incubation in complete darkness, in order to allow the full reversal of NPQ (e.g. Suggett et al. 2003).”
- Direct estimation of functional PSII reaction center concentration and PSII electron flux on a volume basis: a new approach to the analysis of Fast Repetition Rate fluorometry (FRRf) data (2012, background): “2 is qP (e.g., Kolber et al. 1998; Suggett et al. 2001, 2004), which assumes zero connectivity between adjacent RCIIs.”
- Interpretation of fast repetition rate (FRR) fluorescence: signatures of phytoplankton community structure versus physiological state (2009, methodology): “Thus, despite early suggestions (Kolber et al. 1988, Geider et al. 1993a, Kolber & Falkowski 1993), a common maximum value for Fv/Fm cannot be assigned to all algae (see discussion by Suggett et al. 2004).”
- Comparing marine primary production estimates through different methods and development of conversion equations (2014, methodology): “However, assumptions and uncertainties have been reported in the FRRF method (Suggett et al., 2001, 2004; Moore et al., 2003).”
- Different strategies of photoacclimation by two strains of Emiliania huxleyi (Haptophyta) 1 (2007, methodology): “The fluorescence excitation spectrum provides a PSII action spectrum (see Suggett et al. 2004) and consequently characterizes relative values of the effective light absorbed for PSII photochemistry.”
- Biooptical characteristics of PSII and PSI in 33 species (13 pigment groups) of marine phytoplankton, and the relevance for pulse‐amplitude‐modulated and fast‐repetition‐rate fluorometry 1 (2007, methodology): “…of the spectrally integrated optical crosssection of PSII, which we present here as light absorbed by PSII, a PSII (unit m 2 Æ mg chl a)1) to obtain absolute rates of photosynthetic electron transfer (Kroon et al. 1993, Falkowski and Chen 2003, Kromkamp and Forster 2003, Suggett et al. 2004).”
- Comparing electron transport with gas exchange: parameterising exchange rates between alternative photosynthetic currencies for eukaryotic phytoplankton (2009, methodology): “Single-turnover (ST) FRR fluorescence measurements consisting of 100 flashlets of 1.1 µs duration were made every 2 to 3 s, following Suggett et al. (2003, 2004) throughout the illumination period and in the dark immediately after illumination.”