Abstract
Leaves of Kalanchoë pinnata were exposed in the dark to air (allowing the fixation of CO2 into malic acid) or 2% O2, 0% CO2 (preventing malic acid accumulation). They were then exposed to bright light in the presence or absence of external CO2 and light dependent inhibition of photosynthetic properties assessed by changes in 77 K fluorescence from photosystem II (PSII), light response curves and quantum yields of O2 exchange, rates of electron transport from H2O through QB (secondary electron acceptor from the PSII reaction center) in isolated thylakoids, and numbers of functional PSII centers in intact leaf discs. Sun leaves of K. pinnata experienced greater photoinhibition when exposed to high light in the absence of CO2 if malic acid accumulation had been prevented during the previous dark period. Shade leaves experienced a high degree of photoinhibition when exposed to high light regardless of whether malic acid had been allowed to accumulate in the previous dark period or not. Quantum yields were depressed to a greater degree than was 77 K fluorescence from PSII following photoinhibition.
Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Adams W. W., Nishida K., Osmond C. B. Quantum Yields of CAM Plants Measured by Photosynthetic O(2) Exchange. Plant Physiol. 1986 May;81(1):297–300. doi: 10.1104/pp.81.1.297. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Adams W. W., Osmond C. B., Sharkey T. D. Responses of Two CAM Species to Different Irradiances during Growth and Susceptibility to Photoinhibition by High Light. Plant Physiol. 1987 Jan;83(1):213–218. doi: 10.1104/pp.83.1.213. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Arnon D. I. COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS. Plant Physiol. 1949 Jan;24(1):1–15. doi: 10.1104/pp.24.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cockburn W. Relationships between Stomatal Behavior and Internal Carbon Dioxide Concentration in Crassulacean Acid Metabolism Plants. Plant Physiol. 1979 Jun;63(6):1029–1032. doi: 10.1104/pp.63.6.1029. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Davis G. H., MacIvor J., Freeman M. Changes in the vaginal and rectal carriage of group B streptococci during pregnancy. Aust N Z J Obstet Gynaecol. 1980 Feb;20(1):32–34. doi: 10.1111/j.1479-828x.1980.tb00892.x. [DOI] [PubMed] [Google Scholar]
- Demmig B., Winter K., Krüger A., Czygan F. C. Photoinhibition and zeaxanthin formation in intact leaves : a possible role of the xanthophyll cycle in the dissipation of excess light energy. Plant Physiol. 1987 Jun;84(2):218–224. doi: 10.1104/pp.84.2.218. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kitajima M., Butler W. L. Quenching of chlorophyll fluorescence and primary photochemistry in chloroplasts by dibromothymoquinone. Biochim Biophys Acta. 1975 Jan 31;376(1):105–115. doi: 10.1016/0005-2728(75)90209-1. [DOI] [PubMed] [Google Scholar]
- Nobel P. S., Hartsock T. L. Relationships between Photosynthetically Active Radiation, Nocturnal Acid Accumulation, and CO(2) Uptake for a Crassulacean Acid Metabolism Plant, Opuntia ficus-indica. Plant Physiol. 1983 Jan;71(1):71–75. doi: 10.1104/pp.71.1.71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Powles S. B., Osmond C. B. Photoinhibition of intact attached leaves of c(3) plants illuminated in the absence of both carbon dioxide and of photorespiration. Plant Physiol. 1979 Dec;64(6):982–988. doi: 10.1104/pp.64.6.982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Szarek S. R., Johnson H. B., Ting I. P. Drought Adaptation in Opuntia basilaris: Significance of Recycling Carbon through Crassulacean Acid Metabolism. Plant Physiol. 1973 Dec;52(6):539–541. doi: 10.1104/pp.52.6.539. [DOI] [PMC free article] [PubMed] [Google Scholar]