Table 1.
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 |
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 | |
performance index (potential) for energy conservation from photons absorbed by PSII to the reduction of intersystem electron acceptors | |
performance index (potential) for energy conservation from photons absorbed by PSII to the reduction of PSI end acceptors |
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.