When dark-acclimated cotton (Gossypium hirsutum L. cv. Coker 312) leaves, pre-treated with lincomycin to inhibit chloroplast protein repair processes, were exposed to 10 °C and a PPFD of 500 μmol m-2 s-1, the proportion of excitation energy entering photochemistry (P) increased, but only to 5 % of the total energy absorbed at steady state levels of P, which were reached at 40 min of irradiation. Thermal dissipation (D) of absorbed energy increased throughout the 360 min irradiation period and accounted for the greatest portion of absorbed energy at 10 °C. When D was partitioned into constitutive (DCON), regulated (DREG), and photoinhibitory (DPI) components, it was primarily composed of DREG, the readily reversible portion of D. However, the induction of D was slow at 10 °C. Sixty minutes were required for D to reach 70 % of the energy absorbed. Considerable absorption of energy in excess of that utilized in photochemistry or dissipated thermally (designated as E) occurred, especially during induction of P and D. Over the irradiation period, the time-dependent averaged E exhibited an inverse, linear relationship with the ratio of variable (Fv) to maximum (Fm) fluorescence (PS2 efficiency) and a linear relationship with DPI. We propose that time-dependent averaged E may be useful for estimating the potential for damage to PS2 under stressful environmental conditions. and D. Kornyeyev, B. A. Logan, A. S. Holaday.
Based on the examination and quantitative comparison of the approaches used to assess the energy partitioning in photosystem II, the unified method was proposed to calculate the contribution of the components of nonphotochemical quenching. and D. Kornyeyev, C. R. Guadagno, N. D’Ambrosio.
We analyzed several approaches dealing with the components of non-photochemical energy dissipation and introduced improved versions of the equations used to calculate this parameter. The usage of these formulae depends on the conditions of the sample (acclimation to dark or irradiation, presence or absence of the "actinic light"). The parameter known as "excess" cannot be used as a component of energy partitioning. In reality, this parameter reflects the differences between potential and actual quantum yields of photochemistry. and D. Kornyeyev, A. S. Holaday.
Photoinactivation of photosystem 2 (PS2) results from absorption of so-called "excessive" photon energy. Chlorophyll a fluorescence can be applied to quantitatively estimate the portion of excessive photons by means of the parameter E = (F - F0')/Fm', which reflects the share of the absorbed photon energy that reaches the reaction centers (RCs) of PS2 complexes with QA in the reduced state ('closed' RCs). Data obtained for cotton (Gossypium hirsutum), bean (Phaseolus vulgaris), and arabidopsis (Arabidopsis thaliana) suggest a linear relationship between the total amount of the photon energy absorbed in excess (excessive irradiation) and the decline in PS2 activity, though the slope may differ depending on the species. This relationship was sensitive not only to the leaf temperature but also to treatment with methyl viologen. Such observations imply that the intensity of the oxidative stress as well as the plant's ability to detoxify active oxygen species may interact to determine the damaging potential of the excessive photons absorbed by PS2 antennae. Energy partitioning in PS2 complexes was adjusted during adaptation to irradiation and in response to a decrease in leaf temperature to minimize the excitation energy that is trapped by 'closed' PS2 RCs. The same amount of the excessive photons absorbed by PS2 antennae led to a greater decrease in PS2 activity at warmer temperatures, however, the delay in the development of non-photochemical and photochemical energy quenching under lower temperature resulted in faster accumulation of excessive photons during induction. Irradiance response curves of EF suggest that, at high irradiance (above 700 μmol m-2 s-1), steady-state levels of this parameter tend to be similar regardless of the leaf temperature. and D. Kornyeyev, A. S. Holaday, B. A. Logan.