2009
DOI: 10.1016/j.toxicon.2008.10.004
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Detection of microcystin contamination by the measurement of the variability of the in vivo chlorophyll fluorescence in aquatic plant Lemna gibba

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Cited by 14 publications
(5 citation statements)
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“…+ presence of the isoenzyme; ↑ increase of intensity as compared to control; ↓ decrease in intensity as compared to control. Pflugmacher et al, 2007;Järvenpää et al 2007;Saqrane et al, 2009). Pflugmacher (2002) established that the sensitivity of Ceratophyllum demersum to MC-LR is higher than of macroalgae (Cladophora sp.)…”
Section: Discussionmentioning
confidence: 99%
“…+ presence of the isoenzyme; ↑ increase of intensity as compared to control; ↓ decrease in intensity as compared to control. Pflugmacher et al, 2007;Järvenpää et al 2007;Saqrane et al, 2009). Pflugmacher (2002) established that the sensitivity of Ceratophyllum demersum to MC-LR is higher than of macroalgae (Cladophora sp.)…”
Section: Discussionmentioning
confidence: 99%
“…The same has been previously concluded by Ferrante and Maggiore (2007) when they compared chlorophyll fluorescence measurements to anthocyanins, carotenoids and phenolic compounds determination as means to evaluate the quality status of leafy vegetables such as the lettuce Valeriana. Saqrane et al (2009b) has clearly demonstrated the Chl-fluorescence sensitivity to cyanotoxins stress induced in the aquatic plant L. gibba. So, it could be applied to monitor the aquatic ecosystem quality using Lemna as the biotest organism for water quality assessment under aquatic environment preservation programs.…”
Section: Detection Of Microcystins Contamination and Oxidative Stressmentioning
confidence: 96%
“…However, to the best of our knowledge, the use of variable fluorescence as a biophysical indicator of cyanotoxins stress has been rarely reported, particularly in aquatic plants. Only one work was recently published to test the potential use of Chl-fluorescence as a simple biophysical method to evaluate stress induced by cyanotoxins in the aquatic plant L. gibba, following exposure to microcystins (10-300 µg/ml equivalent MC-LR) during 5 h under laboratory conditions (Saqrane et al, 2009b). For terrestrial plants, also a single work that was done to evaluate the physiological state of the photosynthetic apparatus of Brassica oleracea var.…”
Section: Detection Of Microcystins Contamination and Oxidative Stressmentioning
confidence: 99%
“…To date, there are no convincing data on the possible detrimental effects of MCs on the structure of already existing thylakoid membranes or any other internal membrane types of plastid. These alterations are expected due to (i) the abundance of data on the inhibitory effects of MCs and other cyanotoxins on photosynthetic oxygen production and photochemical activities, processes that occur at the level of thylakoids and (ii) the involvement of the PP2A–target of MCs in oxidative stress responses in chloroplasts [ 44 , 45 , 46 ]. However, there is indirect evidence for the interference of MCs with thylakoid biogenesis .…”
Section: Alterations Induced By Cyanotoxins On Peculiar Plant Structuresmentioning
confidence: 99%