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Light and nutrient status of algal cells

Published online by Cambridge University Press:  11 May 2009

M. R. Droop
Affiliation:
Scottish Marine Biological Association, Dunstaffnage Marine Research Laboratory, Oban, Argyll, Scotland, PA34 4AD
M. J. Mickelson
Affiliation:
Scottish Marine Biological Association, Dunstaffnage Marine Research Laboratory, Oban, Argyll, Scotland, PA34 4AD
J. M. Scott
Affiliation:
Scottish Marine Biological Association, Dunstaffnage Marine Research Laboratory, Oban, Argyll, Scotland, PA34 4AD
M. F. Turner
Affiliation:
Scottish Marine Biological Association, Dunstaffnage Marine Research Laboratory, Oban, Argyll, Scotland, PA34 4AD

Extract

Chemostats were used to construct nutrient (vitamin B12) and energy budgets for the flagellate Monochrysis (Pavlova lutheri (Droop) Green) under varying conditions of nutrient and light limitation and luxury, the aim being to describe light limitation and luxury in terms analogous to those of the Cell Quota nutrient model. Measurements were made of steady-state dilution rate, biomass, cell quota, cell chlorophyll a, cell energy content, dark respiration and photosynthetic efficiency, under low irradiance (<13 W per m2).

Cell energy content was 0·54 joules per million cells and was not influenced by growth rate or nutrient/light status. Cell chlorophyll a was 25% less in the nutrient-limited cultures and did not show a clear trend with growth rate except in cultures receiving less than 4·3 W per m2. The effective specific extinction coefficient was 0·12 cm2 per μg chlorophyll. The photosynthesis/irradiance relation was linear. The mean slope (= efficiency) in samples from the light-limited chemostats was 0·225 and was independent of dilution rate. Samples from nutrient-limited chemostats showed a much lower slope, which decreased with decreasing dilution rate. These findings were confirmed by the chemostat kinetic data. Dark respiration varied with dilution rate in a hyperbolic manner and was greater in the nutrient- than the light-limited chemostat.

Light level had no effect on the subsistence quota when the nutrient was limiting, whereas under light-limiting conditions the subsistence quotas were enlarged in inverse proportion to the incident irradiance, thus showing a threshold rather than multiplicative interaction between light and the nutrient.

Energy absorption was very little reduced on nutrient limitation, the great reduction in overall efficiency being associated mainly with the reduction in photosynthetic efficiency.

The reciprocal of photosynthetic efficiency was shown to be analogous to a standardized nutrient cell quota, and an analogous coefficient of luxury could be defined as the ratio of the light-limited to nutrient-limited photosynthetic efficiency at the same growth rate. Thus, light limitation and luxury could be described in terms compatible with the nutrient model without having to introduce new concepts, and a practical criterion between light- and nutrient-limitation could be provided.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1982

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References

REFERENCES

Bannister, T. T., 1974 a. Production equations in terms of chlorophyll concentration, quantum yield, and upper limit to production. Limnology and Oceanography, 19, 112.CrossRefGoogle Scholar
Bannister, T. T., 1974 b. A general theory of steady-state phytoplankton growth in a nutrient saturated mixed layer. Limnology and Oceanography, 19, 1330.CrossRefGoogle Scholar
Bannister, T. T., 1979. Quantitative description of steady-state, nutrient saturated algal growth, including adaptation. Limnology and Oceanography, 24, 7696.CrossRefGoogle Scholar
Conover, R. J., 1978. Transformation of organic matter. In Marine Biology, vol. 4 (ed. Kinne, O.), pp. 221449. Wiley.Google Scholar
Dowd, J. E. & Riggs, D. S., 1965. A comparison of estimates of Michaelis-Menten kinetic constants from various linear transformations. Journal of Biological Chemistry, 240, 863869.CrossRefGoogle ScholarPubMed
Droop, M. R., 1966. Vitamin B12 and marine ecology. III. An experiment with a chemostat. Journal of the Marine Biological Association of the United Kingdom, 46, 659671.CrossRefGoogle Scholar
Droop, M. R., 1968. Vitamin B12 and marine ecology. IV. The kinetics of uptake, growth and inhibition in Monochrysis lutheri. Journal of the Marine Biological Association of the United Kingdom, 48, 689733.CrossRefGoogle Scholar
Droop, M. R., 1974. The nutrient status of algal cells in continuous culture. Journal of the Marine Biological Association of the United Kingdom, 54, 825855.CrossRefGoogle Scholar
Droop, M. R., 1975. The nutrient status of algal cells in batch culture. Journal of the Marine Biological Association of the United Kingdom, 55, 541555.CrossRefGoogle Scholar
Droop, M. R. & Scott, J. M., 1978. Steady-state energetics of a planktonic herbivore. Journal of the Marine Biological Association of the United Kingdom, 58, 749772.CrossRefGoogle Scholar
Falkowski, P. G., 1977. A theoretical description of nitrate uptake kinetics in marine phytoplankton based on bisubstrate kinetics. Journal of Theoretical Biology, 64, 375379.CrossRefGoogle ScholarPubMed
Goering, J. J., Nelson, D. M. & Carter, J. A., 1973. Silicic acid uptake by natural populations of marine phytoplankton. Deep-Sea Research, 20, 777789.Google Scholar
Goldman, J. C. & McCarthy, J. J., 1978. Steady-state growth and ammonium uptake of a fast growing marine diatom. Limnology and Oceanography, 23, 695703.CrossRefGoogle Scholar
Gons, H. J. & Mur, L. R., 1975. An energy balance for algal populations in light limiting conditions. Verhandlungen der Internationalen Vereinigung für theoretische und angewandte Limnologie, 19, 27292733.Google Scholar
Hatchard, G. G. & Parker, C. A., 1956. A new sensitive chemical actinometer. Proceedings of the Royal Society (A), 235, 518533.Google Scholar
Jassby, A. D. & Platt, T., 1976. Mathematical formulation of the relationship between photosynthesis and light for phytoplankton. Limnology and Oceanography, 21, 540547.CrossRefGoogle Scholar
Laws, E. A. & Bannister, T. T., 1980. Nutrient- and light-limited growth of Thalassiosira fluviatilis in continuous culture, with implications for phytoplankton growth in the ocean. Limnology and Oceanography, 25, 457473.CrossRefGoogle Scholar
Laws, E. A. & Caperon, J., 1976. Carbon and nitrogen metabolism by Monochrysis lutheri: measurement of growth-rate-dependent respiration rates. Marine Biology, 36, 8597.CrossRefGoogle Scholar
Lederman, T. & Tett, P. B., 1981. Problems in modelling the photosynthesis-light relationship for phytoplankton. Botanica marina, 24, 125134.CrossRefGoogle Scholar
MacIsaac, J. J. & Dugdale, R. C., 1972. Interactions of light in controlling nitrogen uptake in the sea. Deep-Sea Research, 19, 209232.Google Scholar
Marker, A. F. H., 1965. Extracellular carbohydrate liberation in the flagellates Isochrysis galbana and Prymnesium parvum. Journal of the Marine Biological Association of the United Kingdom, 45, 755772.CrossRefGoogle Scholar
Mickelson, M. J., 1978. Solar radiation in Peru during Joint-II: a guide for modelers. CUEA Technical Report, Duke University, no. 43, 42 pp.Google Scholar
Myers, J., 1953. Growth characteristics of algae in relation to the problems of mass culture. In Algal Culture from Laboratory to Pilot Plant (ed. Burlew, J. S.), pp. 3754. Carnegie Institution of Washington. [Publication 600.]Google Scholar
Pipes, W. O. & Koutsoyannis, S. P., 1962. Light-limited growth of Chlorella in continuous cultures. Applied Microbiology, 10, 15.CrossRefGoogle ScholarPubMed
Platt, T., 1976. Predictability of primary production and budget calculations in coastal inlets. In Population Dynamics of Marine Organisms in Relation with Nutrient Cycling in Shallow Waters, vol. 2. Proceedings of the 10th European Symposium on Marine Biology, Ostend, Belgium, 1975 (ed. Persoone, G. and Jaspers, E.), pp. 477484. Wetteren, Belgium: Universa Press.Google Scholar
Rhee, G-Y. & Gotham, I. J., 1981. The effect of environmental factors on phytoplankton growth: light and the interactions of light with nitrate limitation. Limnology and Oceanography, 26, 649659.CrossRefGoogle Scholar
Scott, J. M., 1975. Calorific measurement of microgram samples of biological material. Laboratory Practice, 24, 657658.Google Scholar
Senft, W. H., 1978. Dependence of light-saturated rates of algal photosynthesis on intracellular concentrations of phosphorus. Limnology and Oceanography, 23, 709718.CrossRefGoogle Scholar
Slobodkin, L. F., 1962. Energy in animal ecology. In Advances in Ecological Research, vol. 1 (ed. Cragg, J. B.), pp. 69101. Academic Press.Google Scholar
Straskraba, M., 1976. Development of an analytical phytoplankton model with parameters empirically related to dominant controlling variables. Abhandlungen der Akademie der Wissenschaften der DDR (Umweltbiophysik), 1974, 3365.Google Scholar
Talling, J. F., 1957. Photosynthetic characteristics of some freshwater plankton diatoms in relation to underwater radiation. New Phytologist, 56, 2950.CrossRefGoogle Scholar
Talling, J. F., 1979. Factor interactions and implications for the prediction of lake metabolism. Archiv für Hydrobiologie, 13, 96109.Google Scholar
Tamiya, H., Iwamura, T., Shibata, J., Hase, H. & Nihei, T., 1953. Correlation between photosynthesis and light-independent metabolism in the growth of Chlorella. Biochimica et biophysica acta, 12, 2340.CrossRefGoogle ScholarPubMed
Tett, P. & Wallis, A., 1978. The general cycle of standing crop in Loch Creran. Journal of Ecology, 66, 227239.CrossRefGoogle Scholar
van Liere, L., 1979. On Oscillatoria agardhii Gomont, Experimental Ecology and Physiology of a Nuisance Bloom-forming Cyanobacterium. Thesis, University of Amsterdam.Google Scholar
Wassink, E. C., Kok, B. & Van Oorschot, J. L. P., 1953. The efficiency of light-energy conversion in Chlorella cultures as compared with higher plants. In Algal Culture from Laboratory to Pilot Plant (ed. Burlew, J. S.), pp. 5562. Carnegie Institution of Washington. [Publication 600.]Google Scholar