FLUORESCENCE‐BASED MAXIMAL QUANTUM YIELD FOR PSII AS A DIAGNOSTIC OF NUTRIENT STRESS

By Jean-Paul Parkhill, G. Maillet, J. Cullen. 2001

529 citations recorded by the source corpus.

Subfields: Ecology, Oceanography, Renewable Energy, Sustainability and the Environment

View Paper: https://www.semanticscholar.org/paper/e3145515e9441797b98436f85d5648beec31b2a6

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Citations in the corpus

Diel variations in the photosynthetic parameters of Prochlorococcus strain PCC 9511: Combined effects of light and cell cycle (2005, background): “The highest Fv/Fm values were around 0.63, a typical value for nutrient-replete cultures in balanced growth (Parkhill et al. 2001).”
Availability of ammonium influences photosynthesis and the accumulation of mycosporine-like amino acids in two Porphyra species (Bangiales, Rhodophyta) (2005, background): “Consistent with other literature, Parkhill et al. (2001) showed that nutrient-replete cultures of phytoplankton had consistently high Fv/Fm values, independent of the irradiance, suggesting that variable fluorescence could be used as a diagnostic tool for nutrient-starved, unbalanced growth…”
Influence of culture medium recycling on the performance of Arthrospira platensis cultures (2015, background): “[25, 34]).”
Physiological responses of three species of marine pico-phytoplankton to ammonium, phosphate, iron and light limitation (2005, background): “The relatively high Fv/Fm values of Synechococcus sp. and P. capsulatus may be explained by the observations that these values may restore themselves by adaptation to nutrient stress (Parkhill et al., 2001).”
Fast repetition rate and pulse amplitude modulation chlorophyll a fluorescence measurements for assessment of photosynthetic electron transport in marine phytoplankton (2003, methodology): “This technique has been used in lakes (e.g. Gilbert et al., 2000), algal cultures (e.g. Parkhill et al., 2001) and microphytobenthos (e.g. Kromkamp et al., 1998, Perkins et al., 2002), but is not sensitive enough for use in oligotrophic, open ocean, conditions.”
Estimating phytoplankton primary production in Lake IJsselmeer (The Netherlands) using variable fluorescence (PAM-FRRF) and C-uptake techniques (2008, background): “…limitation, especially during unbalanced growth conditions, will lower Fv/Fm (Kolber et al., 1988, 1990, 1994; Green et al., 1994; Kromkamp & Peene, 1999; Lippemeier et al., 1999; Parkhill et al., 2001) as well as photoinhibition (Richter et al., 1990; Ohad et al., 1994; Schnettger et al., 1994).”
Taxonomic Discrimination of Phytoplankton by Spectral Fluorescence (2010, background): “These trends may be over-estimates of the true variability, due to an actinic effect of the excitation beam in the fluorometer causing some photosynthetic induction (Parkhill et al. 2001).”
PHOTOSYNTHETIC FUNCTION IN DUNALIELLA TERTIOLECTA (CHLOROPHYTA) DURING A NITROGEN STARVATION AND RECOVERY CYCLE (2003, background): “However, the options for acclimation to N stress under N starvation are restricted relative to N-limitation conditions (Parkhill et al. 2001).”
The elemental stoichiometry and composition of an iron‐limited diatom (2005, methodology): “The ratio of variable to maximum Chl fluorescence (Fv F ) was determined in dark-21m adapted samples using 3-(3,4-dichlorophenyl)-1,1-dimethyl urea (DCMU) to block noncyclic electron flow (Parkhill et al. 2001).”
Photosynthesis and respiration in marine phytoplankton: Relationship with cell size, taxonomic affiliation, and growth phase (2014, unknown): “The Fv/Fm ratio has been extensively use as an indicator of nutrient stress, however, our data supports the view that this ratio does not always give a robust index of nutrient status (Parkhill et al., 2001).”
Interpretation of fast repetition rate (FRR) fluorescence: signatures of phytoplankton community structure versus physiological state (2009, methodology): “Furthermore, values of Fv/Fm can be maintained at the maximal values for a given taxon under nutrient-limited balanced growth (Parkhill et al. 2001).”
Relative influence of nitrogen and phosphorous availability on phytoplankton physiology and productivity in the oligotrophic sub‐tropical North Atlantic Ocean (2008, background): “Thus, the low sensitivity of Fv : Fm to N limitation may indicate that in situ autotrophic populations were in a state of balanced nutrient-limited growth (Parkhill et al. 2001).”
Stress tolerance and antioxidant enzymatic activities in the metabolisms of the reactive oxygen species in two intertidal red algae Grateloupia turuturu and Palmaria palmata (2010, background): “Meanwhile seaweeds could exhibit broad ranges of physiological responses to stressful conditions, notably including the immediate changes in the optimal fluorescence quantum yield (Fv/ Fm) (Parkhill et al., 2001).”
Deciphering the effects of nitrogen, phosphorus, and temperature on cyanobacterial bloom intensification, diversity, and toxicity in western Lake Erie (2019, methodology): “Photosynthetic efficiency, a diagnostic measure of nutrient stress (Parkhill et al. 2001; Simis et al. 2012), was determined by the increase in fluorescence yield from dark-adapted in vivo fluorescence (FV) to maximal DCMU-enhanced (3,4-dichlorophenyl1,1-dimethylurea, photosynthetic inhibitor)…”
Effects of harmful algal blooms on competitors: Allelopathic mechanisms of the red tide dinoflagellate Karenia brevis (2008, background): “A decrease in PSII efficiency has also been reported for a variety of general cell stresses, including nutrient stress (Parkhill et al. 2001), temperature stress (Lesser and Gorbunov 2001), and metal toxicity (Miller-Morey and Van Dolah 2004).”