Abstract
Chlorophyll fluorescence parameters such as Fv/Fm, NPQ and ΦII (YII) are widely used to estimate the fitness and photosynthetic activity of plant leaves and non-photochemical dissipation of excessive excitation energy in photosystem II. The effect of chloroplast movement on these fluorescence parameters reduces the accuracy of estimations of the size of de-excitation processes, but there is no method to calculate correct parameters from altered (fluctuated) parameters. Chloroplast movement was recently identified as the “middle” kinetic component of NPQ. In this paper, we devised a complex but reasonable mathematical method to remove the effect of chloroplast movement on fluorescence parameters, based on our previously reported fluorescence theory. The fraction of “S fluctuation” (designated as σ) was estimated from fluorescence observations and used to calculate the non-fluctuated Fs and F′m. fluorescence yields. From the σ values, the fractional change of light absorbance by a leaf caused by chloroplast movement was estimated at 70% - 100%, which varied according to the experimental conditions and plant species. The effect of photoinhibition on fluorescence parameters was also examined in this paper. The photochemical and non-photochemical de-excitation sizes during photoinhibition (measured by the parameters qPI and qSlow) changed on a single regression line. Using this correlation, qPI and qSlow can be predicted from Fv/Fm, and the non-fluctuated Fm and Fo values can be estimated from the fluctuated F″m and F″o values.
Highlights
2% of the light energy absorbed by a plant’s chlorophyll is emitted as red fluorescence [1]
Such changes can be relatively measured by the pulse amplitude modulation (PAM) method
The first step for calculating the effect of chloroplast movement on non-photochemical quenching (NPQ) size is to introduce the effect of chloroplast movement into the Inverse equation
Summary
2% of the light energy absorbed by a plant’s chlorophyll is emitted as red fluorescence [1]. The fluorescence intensity (or fluorescence yield) of leaf chlorophyll changes according to light conditions because of the photochemical activities of the quenching processes in photosystem II. Such changes can be relatively measured by the pulse amplitude modulation (PAM) method. Several fluorescence parameters such as Fv Fm Fv/Fm, ΦII ( referred to YII in some publications) and NPQ are used to estimate the leaf fitness, rate of photosynthesis, and non-photochemical dissipation of excessive excitation energy [2] [3]. The agricultural significance of the difference in NPQ size is not clear, it may explain the cold tolerance of Japonica cultivars
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