A COMPARISON OF PHOTOSYNTHETIC ELECTRON TRANSPORT RATES IN MACROALGAE MEASURED BY PULSE AMPLITUDE MODULATED CHLOROPHYLL FLUOROMETRY AND MASS SPECTROMETRY

By L. Franklin, M. Badger. 2001

111 citations recorded by the source corpus.

Subfields: Oceanography, Renewable Energy, Sustainability and the Environment

View Paper: https://www.semanticscholar.org/paper/ae7dec4dc262da1f53da66985c95bf90a19b1e86

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In Oceanography

In Renewable Energy, Sustainability and the Environment

Citations in the corpus

Limitations in the use of PAM fluorometry for measuring photosynthetic rates of macroalgae at high irradiances (2004, background): “However, as pointed out by Franklin & Badger (2001), and further elaborated on by Longstaff et al. (2002) for Ulva lactuca, this explanation may have to be modified, and different causes may underlie such a response in different species.”
Influence of temperature on the relationship between oxygen- and fluorescence-based estimates of photosynthetic parameters in a marine benthic diatom (Cylindrotheca closterium) (2003, background): “…have suggested that cyclic electron flow around PSII or nonphotochemical energy quenching within PSII centres are more likely causes of non-linearity than oxygen consuming processes (e.g. Mehler-ascorbate-peroxidase reaction; Ruuska et al. 2000, Badger et al. 2000, Franklin & Badger, 2001).”
Fast repetition rate and pulse amplitude modulation chlorophyll a fluorescence measurements for assessment of photosynthetic electron transport in marine phytoplankton (2003, methodology): “…the non-linearity reported between measured quantum yields of oxygen evolution and (Fq’/ Fm’)/k determined by PAM fluorescence (Flameling & Kromkamp, 1998; Franklin & Badger, 2001; Masojı́dek et al., 2001) may partly be attributable to the differences in the ST versus MT protocols.”
The Use of the Fluorescence Signal in Studies of Seagrasses and Macroalgae (2010, background): “Deviations from the linearity have been frequently reported dependent on species, light history, irradiance, tissue thickness, and other factors such as CO 2 and nitrate levels (e.g., Beer et al. 1998; Beer and Björk 2000; Franklin and Badger 2001; Beer and Axelsson 2004; Enríquez and Rodríguez-Romá”
Chlorophyll Fluorescence in Reef Building Corals (2010, background): “in algae (Geel et al. 1997; Flameling and Kromkamp 1998; Franklin and Badger 2001; Hancke et al. 2008a, b), ETR calculated from corals can significantly overestimate photosynthetic productivity over a broad range of light intensities (Hoogenboom et al. 2006), including those well below the level f”
Comparing electron transport with gas exchange: parameterising exchange rates between alternative photosynthetic currencies for eukaryotic phytoplankton (2009, methodology): “…studies included additional measurements of absorption, enabling ETRPSII to be compared with corresponding photosynthesis rates obtained via O2 evolution (Beer et al. 1998, Franklin & Badger 2001, Suggett et al. 2001) and C uptake (Kolber & Falkowski 1993, Boyd et al. 1997, Hartig et al. 1998).”
AMMONIUM AND UV RADIATION STIMULATE THE ACCUMULATION OF MYCOSPORINE‐LIKE AMINO ACIDS IN PORPHYRA COLUMBINA (RHODOPHYTA) FROM PATAGONIA, ARGENTINA 1 (2004, methodology): “…irradiances, ETR calculated from FPSII closely matches gross O2 evolution in different Ulva species and Porphyra columbina (Beer et al. 2000, Franklin and Badger 2001), but in Ulva lactuca at higher irradiances the relation ETR/GP increased up the theoretical value of 4 (Longstaff et al.…”