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Inhibition of photosynthesis by freezing temperatures and high light levels in cold‐acclimated seedlings of Scots pine ( Pinus sylvestris ). – II. Effects on chlorophyll fluorescence at room temperature and 77 K.
Author(s) -
Strand Martin,
Öquist Gunnar
Publication year - 1985
Publication title -
physiologia plantarum
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.351
H-Index - 146
eISSN - 1399-3054
pISSN - 0031-9317
DOI - 10.1111/j.1399-3054.1985.tb02369.x
Subject(s) - photosystem ii , photoinhibition , chlorophyll fluorescence , photosynthesis , scots pine , photosystem i , botany , chemistry , electron transport chain , thylakoid , photochemistry , biology , pinus <genus> , chloroplast , biochemistry , gene
Shoots of cold‐acclimated seedlings of Pinus sylvestris L. were exposed to a temperature of –7°C for 4 h, in darkness or at a photon flux density of 1 300 μmol m ‐2 s ‐1 . Before and after freezing, fluorescence kinetics of intact needles and isolated chloroplast membranes were measured at both room temperature and 77 K. Maximum and variable fluorescence yield of photosystem II both at room temperature and 77 K decreased strongly after freezing in light, whereas the initial fluorescence yield was little affected. Quenching of maximum and variable fluorescence of photosystem I at 77 K also occurred. The results show that freezing in light damages photosystem II, thereby increasing the radiationless decay at the reaction centres of photosystem II. This is a typical symptom of photoinhibition of photosynthesis. Freezing in darkness did not significantly reduce fluorescence yield of photosystem II or photosystem I. Moreover, electron transport capacity was not significantly affected. We therefore suggest that the inhibition of the CO 2 assimilation in pine seedlings by freezing alone does not involve thylakoid inactivation.