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The effect of pro longed illumination (60 min) with photosynthetically active monochromatic radiation of low intensity (3 μmol-m⁻² ·s⁻¹) and high intensity (60 mmol m⁻² ·s⁻¹), corresponding to the physiological conditions and light stress conditions, respectively, was studied in the algae Nitellopsis obtusa. Illumination of Nitellopsis obtusa cells with strong light was associated with activation of the xanthophyll cycle, manifested by the deepoxidation of violaxanthin and accumulation of antheraxanthin and zeaxanthin. At the same time, the efficient singlet excitation quenching in the photosynthetic apparatus was activated, as demonstrated by the decrease in the intensity of the chlorophyll a fluorescence emission by ca 50 %. The difference of the fluorescence excitation spectra recorded before and after the light treatment match the difference absorption spectrum of the xanthophyll cycle pigments. The illumination with low light intensity resulted also in the chlorophyll a fluorescence quenching but the effect was very small (less than 10 %). The fluorescence quenching is interpreted in terms of the energy transfer between the Qy energy level of chlorophyll a and the 2¹Ag⁻ energy level of zeaxanthin. The singlet energy levels of carotenoids, corresponding to the green spectral region, are also taken into consideration in the interpretation of the excitation energy exchange between the carotenoids and chlorophylls. Possible molecular mechanisms involved in the activation of the strong and the weak excitation quenching, including violaxanthin isomerization, and possible physiological functions of such pathways of energy transfer are discussed.
Ultraweak luminescence (UL) within the visible range accompanies physiological processes taking place in Native non-stressed Nitellopsis Obtusa cells. Intensity of UL emission is several times higher than the intensity of an environmental medium. The influence of Humic acid (HA), diuron-urea herbicide (DCMU) and photosynthetic active radiation (PAR) on UL intensity and spectral composition for algae cells was investigated. Measurements were made both in neutral and reactive media. An artificial pond water (APW) served as a neutral medium. Algae cells in APW were used as the control samples. Concentrations of specific chemical agents were equal to 8·10-2mg·mL-1, 4.2·10-2 mmol·L-1 for HA and DCMU, respectively, whereas PAR intensity reached 900 µE·s-1·m-2. The influence of HA and light on UL intensity was studied.
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