Abstract
A new method of the chlorophyll (Chl) a fluorescence quenching analysis is described, which allows the calculation of values of (at least) three components of the non-photochemical quenching of the variable Chl a fluorescence (q N) using a non-linear regression of a multi-exponential function within experimental data. Formulae for coefficients of the “energy”-dependent (∆pH-dependent) quenching (q E), the state-transition quenching (q T) and the photo/inhibitory quenching (q I) of Chl a fluorescence were found on the basis of three assumptions: (i) the dark relaxation kinetics of q N, as well as of all its components, is of an exponential nature, (ii) the superposition principle is valid for individual Chl a fluorescence quenching processes and (iii) the same reference fluorescence level (namely the maximum variable Chl a fluorescence yield in the dark-adapted state, F V) is used to define both q N and its components. All definitions as well as the algorithms for analytical recognition of the q N components are theoretically clarified and experimentally tested. The described theory results in a rather simple equation allowing to compute values for all q N components (q E, q T, q I) as well as the half-times of relaxation (τ1/2) of corresponding quenching processes. It is demonstrated that under the above assumptions it holds: q N = q E + q T + q I. The theoretically derived equations are tested, and the results obtained are discussed for non-stressed and stressed photosynthetically active samples. Semi-empirical formulae for a fast estimation of values of the q N components from experimental data are also given.