Plant and Cell Physiology, 1986, Vol. 27, No. 7 1335-1349
© 1986
Article |
Light Harvesting and Utilization by Phytoplankton
1Department of Life Sciences, Bar Ilan University Ramat Can, Israel 52100
2Oceanographic Sciences Division, Brookhaven National Laboratory Upton, New York 11973, U.S.A.
In this study we use a model based on target theory to analyze steady-state photosynthesis-irradiance relationships in continuous light. From the average turnover time (
) of photosynthetic units (PSUO2), numerical analyses of the model coefficients, and measurements of the light field and cell absorptivity, apparent absorption crosssections of photosystem II (
PSII) were determined for three species of marine unicellular algae grown at different irradiance levels. These cross-sections generally, but not always, increased with decreased growth irradiance. Additionally, the ratios of photosystem I/photosystem II reaction centers were calculated from measurements of oxygen flash yields and chlorophyll/P700 ratios. From the ratios of the reaction centers, cell absorptivity and the apparent absorption cross-section of photosystem II, the apparent absorption cross-sections of photosystem I (
PSI) were also calculated. Finally, on the basis of our calculated absorption cross-sections, we estimated the minimum quantum requirements for O2 evolution. Our results suggest that the absorption cross-sections of PS I and PS II vary independently and the minimum quantum requirements for O2 vary by more than twofold, increasing from 9.1 to 20.6 quanta/O2, as growth irradiance increases. The increase in quantum requirement corresponds to larger apparent cross-sections for photosystem I and higher carotenoid/chlorophyll ratios.
(Received October 15, 1985; Accepted July 17, 1986)
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
T. Fujiki, T. Suzue, H. Kimoto, and T. Saino Photosynthetic electron transport in Dunaliella tertiolecta (Chlorophyceae) measured by fast repetition rate fluorometry: relation to carbon assimilation J. Plankton Res., February 1, 2007; 29(2): 199 - 208. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Adolf, D. K. Stoecker, and L. W. Harding Jr The balance of autotrophy and heterotrophy during mixotrophic growth of Karlodinium micrum (Dinophyceae) J. Plankton Res., August 1, 2006; 28(8): 737 - 751. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Malinsky-Rushansky, T. Berman, T. Berner, Y. Z. Yacobi, and Z. Dubinsky Physiological characteristics of picophytoplankton, isolated from Lake Kinneret: responses to light and temperature J. Plankton Res., November 1, 2002; 24(11): 1173 - 1183. [Abstract] [Full Text] [PDF] |
||||
![]() |
B.-P. Han, M. Virtanen, J. Koponen, and M. Straskraba Effect of photoinhibition on algal photosynthesis: a dynamic model J. Plankton Res., May 1, 2000; 22(5): 865 - 885. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Behrenfeld and Z. S. Kolber Widespread Iron Limitation of Phytoplankton in the South Pacific Ocean Science, February 5, 1999; 283(5403): 840 - 843. [Abstract] [Full Text] |
||||
![]() |
A. Lardans, B. Forster, O. Prasil, P. G. Falkowski, V. Sobolev, M. Edelman, C. B. Osmond, N. W. Gillham, and J. E. Boynton Biophysical, Biochemical, and Physiological Characterization of Chlamydomonas reinhardtii Mutants with Amino Acid Substitutions at the Ala251 Residue in the D1 Protein That Result in Varying Levels of Photosynthetic Competence J. Biol. Chem., May 1, 1998; 273(18): 11082 - 11091. [Abstract] [Full Text] [PDF] |
||||


