“…For Symbiodinium, these processes are much less characterized than in higher plants or green algae (Warner and Suggett, 2016), but evidence suggests that alternative electron transport can manifest itself in Abbreviations: DCMU, 3-(3,4-dichlorophenyl)-1,1-dimethyl-urea; FR, far red light; F o , intrinsic fluorescence signal with fully oxidized Q A in the dark; F m , maximal fluorescence signal with fully reduced Q A ; F v , Variable fluorescence in the dark (proportional to reducible Q A ); GA, glycolaldehyde; F v /F m , Maximum quantum efficiency of open PSII centers in the dark based on full Q A reduction; MT, multiple turnover; LIFT-FRRF, laser-induced fluorescence transient fast repetition rate fluorometry; PAR, photosynthetically active radiation (400-700 nm); PSII, photosystem II; PSI, photosystem I; P700, special chlorophyll dimer acting as the primary electron donor in PSI; P700 + , oxidized state of P700; P m , maximum P700 + signal in weak FR light; PQ, plastoquinone pool σ PSIIfunctional absorption cross section of PSII in the dark; Q A , primary quinone electron acceptor in PSII; Q B , secondary quinone electron acceptor in PS II; NIR, near infrared light; ST, single turnover. the form of cyclic electron flow (CEF) operating between PSI and the cytochrome b 6 /f complex possibly via the ferredoxindependent pathway (Aihara et al, 2016), or pseudo-cyclic electron flow of Mehler reaction, that plays a significant role in excess energy dissipation (Roberty et al, 2014). Expression of these pathways, however, may differ significantly between different Symbiodinium genotypes (Aihara et al, 2016;Warner and Suggett, 2016).…”