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Diel patterns of carbon incorporation into biochemical constituents of Synechococcus spp. and larger algae in the Northwest Atlantic Ocean

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Abstract

Diel patterns of 14C-bicarbonate incorporation in>5 μm algal communities were compared with those in cyanobacterial populations of Synechococcus spp. (0.6 to 1.0 μm), collected from the surface and/or chlorophyll maximum at three stations in the Northwest Atlantic Ocean (a neritic front; in Warm-Core Eddy 84-E; and Wilkinson's Basin) from 21 July to 8 August, 1984. Cell constituents were chemically separated into four fractions: lipids, low molecular weight (LMW) metabolites, polysaccharides/nucleic acids, and proteins. The in situ diel pattern of 14C assimilation was virtually the same for >5 μm algal communities adapted to different environments. Protein synthesis appeared to continue at a reduced rate at night using energy derived from the catabolism of polysaccharides and the mobilization of LMW compounds. Synechococcus spp. populations exhibited inherent physiological differences in their in situ diel pattern of carbon fixation from that in>5 μm algal communities taken from the same water mass. There was no nighttime protein-synthesis in Synechococcus spp. The relative proportion of 14C-protein remained constant over night, while that of 14C-polysaccharides/nucleic acids declined and that of labelled LMW metabolites increased. Daytime light-intensity manipulations did not alter the diel pattern of carbon fixation in any of the>5 μm algal assemblages, while changes in the carbon metabolism of surface and shadeadapted Synechococcus spp. populations could be rapidly induced by altering the light intensity.

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Literature cited

  • Barlow, R. G. (1984). Time-series uptake of carbon into photosynthetic products of Benguela phytoplankton populations. J. Plankton Res. 6: 435–442

    Google Scholar 

  • Cuhel, R. L., Ortner, P. B., Lean, D. R. S. (1984). Night synthesis of protein by algae. Limnol. Oceanogr. 29: 731–744

    Google Scholar 

  • Cuhel, R. L., Waterbury, J. B. (1984). Biochemical composition and short-term nutrient incorporation patterns in a cellular marine cyanobacterium, Synechococcus (WH7803). Limnol. Oceanogr. 29: 370–374

    Google Scholar 

  • DiTullio, G. R., Laws, E. A. (1986). diel periodicity of nitrogen and carbon assimilation in five species of marine phytoplankton: accurracy of methodology for predicting N-assimilation rates and N/C composition ratios. Mar. Ecol. Prog. Ser. 32: 123–132

    Google Scholar 

  • Glover, H. E. (1985). The physiology and ecology of the marine cyanobacterial genus Synechococcus. In: Jannasch, H. W., Williams, P. J.LeB. (eds.) Advances in aquatic microbiology, Vol. 3. Academic Press, London, p. 49–107

    Google Scholar 

  • Glover, H. E., Campbell, L., Prézelin, B. B. (1986). Contribution of Synechococcus spp. to size-fractioned primary productivity in three water masses in the Northwest Atlantic Ocean. Mar. Biol. 91: 193–203

    Google Scholar 

  • Glover, H. E., Phinney, D. A., Yentsch, C. S. (1985). Photosynthetic characteristics of picoplankton compared with those of larger phytoplankton populations in various water masses in the Gulf of Maine. Biol. Oceanogr. 3: 223–248

    Google Scholar 

  • Harding, L. W., Jr., Meeson, B. W., Fisher, T. R., Jr. (1985). Patterns of photosynthetic carbon metabolism in light-limited phytoplankton. Mar. Biol. 89: 121–133

    Google Scholar 

  • Lancelot, C., Billen, G. (1985). Carbon-nitrogen relationships in nutrient metabolism of coastal marine ecosystems. In: Jannasch, H. W., Williams, P. J. Leb. (eds.) Advances in aquatic microbiology, Vol. 3. Academic Press, London/New York, p. 263–322

    Google Scholar 

  • Lancelot, C., Mathot, S. (1985). Biochemical fractionation of primary production by phytoplankton in Belgian coastal waters during short- and long-term incubations with 14C-bicarbonate. I. Mixed diatom population. Mar. Biol. 86: 219–226

    Google Scholar 

  • Li, W. K. W., Subba-Rao, D. V., Harrison, W. G., Smith, J. C., Cullen, J., Irwin, B., Platt, T. (1983). Autotrophic picoplankton in the tropical ocean. Science, N.Y. 219: 292–295

    Google Scholar 

  • Morris, I. (1981). Photosynthesis products, physiological state and phytoplankton growth. Can. Bull. Fish. aquat. Sciences 210: 83–102

    Google Scholar 

  • Morris, I., Glover, H. E., Yentsch, C. S. (1974). Products of photosynthesis by marine phytoplankton: the effect of environmental factors on the relative rates of protein synthesis. Mar. Biol. 27: 1–9

    Google Scholar 

  • Morris, I., Skea, W. (1978). Products of photosynthesis in natural populations of marine phytoplankton from the Gulf of Maine. Mar. Biol. 47: 303–312

    Google Scholar 

  • Morris, I., Smith, A. E., Glover, H. E. (1981). Products of photosynthesis in phytoplankton off the Orinoco River and in the Caribbean Sea. Limnol. Oceanogr. 26: 1034–1044

    Google Scholar 

  • Platt, I., Subba-Rao, D. V., Irwin, B. (1983). Photosynthesis of picoplankton in the oligotrophic ocean. Nature, Lond. 301: 702–704

    Google Scholar 

  • Post, A. F., Loogman, J. G., Mur, L. R. (1985). Regulation of growth and photosynthesis by Oscillatoria agardhii grown with a light/dark cycle. Fedn. eur. microbiol. Soc. (FEMS) Microbiol. Ecol. 31: 97–102

    Google Scholar 

  • Prézelin, B. B., Glover, H. E., Campbell, L. (1987). Effects of light intensity and nutrient availability on diel patterns of cell metabolism and growth in populations of Synechococcus spp. Mar. Biol. 95: 469–480

    Google Scholar 

  • Prézelin, B. B., Putt, M., Glover, H. E. (1986). Diurnal patterns in photosynthetic capacity and depth-dependent photosynthesisirradiance relationships in Synechococcus spp. and larger phytoplankton in three water masses in the Northwest Atlantic Ocean. Mar. Biol. 91: 205–217

    Google Scholar 

  • Priscu, J. C., Goldman, C. R. (1983). Carboxylating enzyme activity and photosynthetic end products of phytoplankton in the shallow and deep chlorophyll layers of Castle Lake. Limnol. Oceanogr. 28: 1168–1181

    Google Scholar 

  • Rivkin, R. B. (1985). Carbon-14 labelling patterns of individual marine phytoplankton from natural populations. Mar. Biol. 89: 135–142

    Google Scholar 

  • Smith, A. J. (1982). Modes of cyanobacterial carbon metabolism. In: Carr, N. G., Whitton, B. A. (eds.) The biology of cyanobacteria. University of California Press, Berkeley, p. 47–85

    Google Scholar 

  • Smith, R. C., Baker, K. S., Dunstan, P. (1981). Fluorometric techniques for the measurement of ocean chlorophyll in the support of remote sensing. Ref. Rep. Scripps Instn Oceanogr. 81-17:1–14

    Google Scholar 

  • Waterbury, J. B., Watson, S. W., Valois, F. W., Franks, D. G. (1986). Biological and ecological characterization of the marine unicellular cyanobacterium Synechococcus. Can. Bull. Fish. aquat. Sciences 214: 71–120

    Google Scholar 

  • Yentsch, C. S., Menzel, D. W. (1963). A method for the determination of phytoplankton chlorophyll and phaeophytin by fluorescence. Deep-Sea Res. 10: 443–448

    Google Scholar 

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Communicated by R. S. Carney, Baton Rouge

Bigelow Laboratory Contribution No. 86004

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Glover, H.E., Smith, A.E. Diel patterns of carbon incorporation into biochemical constituents of Synechococcus spp. and larger algae in the Northwest Atlantic Ocean. Mar. Biol. 97, 259–267 (1988). https://doi.org/10.1007/BF00391311

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