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. 2020 Jan 17;10:1688. doi: 10.3389/fpls.2019.01688

Table 1.

Formulae and explanation of the technical data of the OJIP curves and the selected JIP-test parameters used in this studya.

Technical fluorescence parameters
Ft fluorescence at time t after onset of actinic illumination
FO ≅ F20µs minimal fluorescence, when all PSII RCs are open
FL ≡ F150µs fluorescence intensity at the L-step (150 µs) of OJIP
FK ≡ F300µs fluorescence intensity at the K-step (300 µs) of OJIP
FJ ≡ F2ms fluorescence intensity at the J-step (2 ms) of OJIP
FI ≡ F30ms fluorescence intensity at the I-step (30 ms) of OJIP
FP (= FM) maximal recorded fluorescence intensity, at the peak P of OJIP
Fv ≡ Ft – FO variable fluorescence at time t
FV ≡ FM – FO maximal variable fluorescence
tFM time (in ms) to reach the maximal fluorescence intensity FM
Vt ≡ (Ft – FO)/(FM – FO) relative variable fluorescence at time t
VK = (FK – FO)/(FM – FO) relative variable fluorescence at the K-step
VJ = (FJ – FO)/(FM – FO) relative variable fluorescence at the J-step
Wt ≡ (Ft – FO)/(FJ – FO) relative variable fluorescence Fv to the amplitude FJ – FO
WOK = (Ft – FO)/(FK – FO) ratio of variable fluorescence Ft – FO to the amplitude FK – FO
WOJ = (Ft – FO)/(FJ – FO) ratio of variable fluorescence Ft – FO to the amplitude FJ – FO
WOI = (Ft – FO)/(FI – FO) ratio of variable fluorescence Ft – FO to the amplitude FI – FO
WIP = (Ft – FI)/(FP – FI) ratio of variable fluorescence Ft – FI to the amplitude FP– FI
M0 ≡ 4(F270μs – FO)/(FM – FO) approximated initial slope (in ms–1) of the fluorescence transient normalized on the maximal variable fluorescence FV
Sm ≡ Area/(FM – FO) normalized total complementary area above the O-J-I-P transient (reflecting multiple-turnover QA reduction events)
Ss = VJ/M0 normalized total complementary area corresponding only to the O-J phase (reflecting single-turnover QA reduction events)
Quantum efficiencies or flux ratios
φPo = PHI(P0) = TR0/ABS = 1– FO/FM maximum quantum yield for primary photochemistry
ψEo = PSI0 = ET0/TR0 = 1–VJ probability that an electron moves further than QA
φEo = PHI(E0) = ET0/ABS = (1– FO/FM) (1–VJ) quantum yield for electron transport (ET)
φDo = PHI(D0) = 1- φPo = FO/FM quantum yield (at t = 0) of energy dissipation
φRo = RE0/ABS = φPo. ψEo. δRo = φPo. (1–VI) quantum yield for reduction of the end electron acceptors at the PSI acceptor side (RE)
δRo = RE0/ET0 = (1 – VI)/(1 – VJ) probability that an electron is transported from the reduced intersystem electron acceptors to the final electron acceptors of PSI
γRC = ChlRC/Chltotal = RC/(ABS+RC) probability that a PSII Chl molecule functions as RC
Phenomenological energy fluxes (per excited leaf cross-section-CS)
ABS/CS = Chl/CS absorption flux per CS
TR0/CS = φPo. (ABS/CS) trapped energy flux per CS
ET0/CS = φPo. ψEo. (ABS/CS) electron transport flux per CS
Density of RCs
RC/CS = φPo. (VJ/M0). (ABS/CS) QA-reducing RCs per CS
QA-reducing centers = (RC/RCreference).(ABS/ABSreference) = [(RC/CS)treatment/(RC/CS)control]. [(ABS/CS)treatment/(ABS/CS)control] The fraction of QA-reducing reaction centers
Non-QA-reducing centers = 1- QA-reducing centers The fraction of non-QA-reducing reaction centers, also so-called heat sink centers or silent centers
Sm/tFM = [RCopen/(RCclose + RCopen)]av = [QA/QA(total)]av average fraction of open RCs of PSII in the time span between 0 to t FM
RJ = [ψEo (control) − ψEo (treatment)]/ψEo (control) = [VJ (treatment) – VJ (control)]/[1 − VJ (control)] number of PSII RCs with QB-site filled by PSII inhibitor
Performance indexes
PIABSγRC1γRC·φPo1φPo·ψEo1ψEo performance index (potential) for energy conservation from photons absorbed by PSII to the reduction of intersystem electron acceptors
PItotalPIABSδRo1δRo performance index (potential) for energy conservation from photons absorbed by PSII to the reduction of PSI end acceptors
a

Subscript “0” (or “o” when written after another subscript) indicates that the parameter refers to the onset of illumination, when all RCs are assumed to be open.