In a study of the relationship between nonphotochemical quenching of fluorescence and the xanthophyll cycle, we show that the diatom Phaeodactylum tricornutum exhibits several interesting characteristics. This xanthophyll cycle consists of only one reversible epoxidating/deepoxidating step (diadinoxanthiddiatoxanthin). Diadinoxan‐thin, which increases from 8 to 17 molecules/100 chlorophyll a (Chl a) during the ageing of the culture, was present as two separate pools, with a portion (of about 5 molecules/100 Chl a) which was never deepoxidated. Under a defined irradiance, the time necessary to abolish net photosynthesis increases with the pool size of diadinoxanthin available for deepoxidation. A close correlation is found between nonphotochemical quenching and the relative ratio of diatoxanthin until the photosytem II center is inactivated. The photoprotective effect of diadinoxanthin deepoxidation is limited to the phase during which quenching of the minimum fluorescence (F0) develops.

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A new fluorometric device was developed to measure the fluorescence yield of microalgae in order to detect photosystem II specific herbicides in outdoor water samples. The system was tested with respect to sensitivity and reliability with two species: Chlorella fusca (a green alga) and Phaeodactylum tricornutum (a diatom). The main advantages are the use of cell cultures without preliminary centrifugation, the evaluation of variable fluorescence from steady-state levels, and the rapidity of the measurement. Concentrations around the binding constant of inhibitors (around 10 -8 M) can be detected for dichlorophenlydimethylurea, atrazine and simazine. The new system was compared with the commercially available pulse amplitude fluorometer PAM IOI; it was shown that the sensitivity was about 10 times greater than with PAM 101, working at optimal chlorophyll concentrations. The advantages and limits of both systems when applied to flee-water samples are discussed.