Photoprotection of PSII in Hawaiian lobeliads from diverse light environments

2008 ◽  
Vol 35 (7) ◽  
pp. 595 ◽  
Author(s):  
Rebecca A. Montgomery ◽  
Guillermo Goldstein ◽  
Thomas J. Givnish

Excess irradiance can reduce the quantum yield of photosynthesis via photoprotective energy dissipation, inactivation or downregulation of PSII. We examined variation in photoprotection as part of a study of adaptive radiation in photosynthetic light responses by Hawaiian lobeliads. We measured the maximum efficiency of PSII (Fv/Fm) and recovery of Fv/Fm after high light stress in field populations of 11 lobeliad species and in four species growing under common-garden greenhouse conditions. Species showed no difference in Fv/Fm (0.82 ± 0.02 (mean ± s.e.)) or in their ability to recover from light stress under field conditions. Average recovery was 74 ± 1.4% within 1 h of removal of the stress suggesting that all species maintain the ability to recover from high light stress, at least in the short-term. In contrast, the results from the common-garden indicate that long-term exposure to high irradiance and associated higher temperatures can cause a sustained reduction in PSII function. Species showed decreased Fv/Fm and percentage recovery as treatment irradiance increased. Fv/Fm and percentage recovery were positively related to native habitat PFD across species, suggesting that there has been a diversification in high light tolerance, with species from sunnier environments better able to avoid sustained declines in PSII function.

2019 ◽  
Vol 57 (3) ◽  
pp. 830-840 ◽  
Author(s):  
Y.N. LIU ◽  
Q.Z. XU ◽  
W.C. LI ◽  
X.H. YANG ◽  
Q. ZHENG ◽  
...  

2012 ◽  
Vol 2 (1) ◽  
pp. 42-51 ◽  
Author(s):  
Miloš Barták ◽  
Josef Hájek ◽  
Petra Očenášová

The paper deals with the differences in sensitivity of Antarctic lichen to photoinhibition. Thalli of Usnea antarctica were collected at the James Ross Island, Antarctica (57°52´57´´W, 63°48´02´´S) and transferred in dry state to the Czech Republic. After rewetting in a laboratory, they were exposed to 2 high light treatments: short-term (30 min), and long-term (6 h). In short-term treatment, the sample were exposed to 1000 and 2000 µmol m-2 s-1 of photosynthetically active radiation (PAR). In long-term experiment, PAR of 300, 600, and 1000 µmol m-2 s-1 were used. Photosynthetic efficiency of U. antarctica thalli was monitored by chlorophyll fluorescence parameters, potential (FV/FM) and actual (FPSII) quantum yield of photochemical processes in photosystem II in particular. In short-term treatments, the F0, FV and FM signals, as well as the values of FV/FM, and FPSII showed light-induced decrease, however substantial recovery after consequent 30 min. in dark. Longer exposition (60 min) to high light led to more pronounced decrease in chlorophyll fluorescence than after 30 min treatment, however dark recovery was faster in the thalli treated before for longer time (60 min). Long-term treatment by high light caused gradual decrease in FV/FM and FPSII with the time of exposition. The extent of the decrease was found light dose-dependent. The time course was biphasic for FV/FM but not for FPSII. The study showed that wet thalli of Usnea antarctica had high capacity of photoprotective mechanisms to cope well either with short- or long-term high light stress. This might be of particular importance in the field at the James Ross Island, particularly at the begining of growing season when melting water is available and, simultaneously, high light stress may happen on fully sunny days.


2013 ◽  
Vol 162 ◽  
pp. 1-10 ◽  
Author(s):  
Yuefei Xu ◽  
Juanjuan Fu ◽  
Xitong Chu ◽  
Yongfang Sun ◽  
He Zhou ◽  
...  

1998 ◽  
Vol 53 (1-2) ◽  
pp. 93-100 ◽  
Author(s):  
Lu Fan ◽  
Avigad Vonshak ◽  
Aliza Zarka ◽  
Sammy Boussiba

Abstract The photoprotective function of the ketocarotenoid astaxanthin in Haematococcus was questioned. When exposed to high irradiance and/or nutritional stress, green Haematococcus cells turned red due to accumulation of an immense quantity of the red pigment astaxanthin. Our results demonstrate that: 1) The addition of diphenylamine, an inhibitor of astaxanthin biosynthesis, causes cell death under high light intensity; 2) Red cells are susceptible to high light stress to the same extent or even higher then green ones upon exposure to a very high light intensity (4000 μmol photon m-2 s-1); 3) Addition of 1O2 generators (methylene blue, rose bengal) under noninductive conditions (low light of 100 (μmol photon m-2 s-1) induced astaxanthin accumulation. This can be reversed by an exogenous 1O2 quencher (histidine); 4) Histidine can prevent the accumulation of astaxanthin induced by phosphate starvation. We suggest that: 1) Astaxanthin is the result of the photoprotection process rather than the protective agent; 2) 1O2 is involved indirectly in astaxanthin accumulation process.


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