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Kinetics of alkaline phosphatase activity and phosphorus availability for phytoplankton and bacterioplankton in lake plu\see (North German Eutrophic Lake)

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Abstract

Annual studies of kinetics of alkaline phosphatase (APA) activity and phosphorus availability for microplankton in the photic zone of an eutrophic lake are reported. The total APA activity of microplankton varied strongly. Vmax was highest during summer P depletion, and in autumn and winter total APA activity was low. The total APA specific activity of the microplankton was also highest (average 3.55 pmole PO4 3− ng ATP−1 min−1) when ambient orthophosphate concentrations were very low. Both Vmax and specific APA activity were not dependent on the biomass of microplankton; they were strongly affected by P available for microplankton. A differential filtration technique was used for separation of microplankton into two size classes, i.e., algal, larger than 3μm, and bacterial fraction with size 0.2–3.0μm. The algal size fraction had lower specific APA activity (average 1.224 pmole PO4 3− ng ATP−1 min−1) and higher KM values (38.8μmole × liter−1) than microorganisms which were smaller than 3μm (2.011 pmole PO4 3− ng ATP−1 min−1 and 25.4μmole liter−1, respectively). The KM values of free, dissolved APA (36.8μmole liter−1) indicated that free APA was probably released by algae. Phytoplankton were major APA activity producers in the photic zone of the lake from March to November, and their activity constituted, on the average, 48.6% of the total APA activity in the water. Bacteria were the dominant APA activity producers in winter (41.3–44.9%); however, during other periods they contributed significantly (average 21.7%) to total APA activity. When surplus constituted less than 10% of particulate P in seston, phytoplankton produced high specific APA activity, and when surplus P was higher than 15%, the specific APA activity of phytoplankton size fraction rapidly decreased. APA of the bacterial size fraction of the seston was not affected by P concentrations. Orthophosphate was a competitive inhibitor of APA produced by microorganisms of the size fraction larger than 3.0μm, and increasing concentrations of inorganic phosphate caused an increase in KM values. The hypothetical metabolic-coupling between phytoplankton and bacterioplankton in the phosphorus cycle in conjunction with carbon metabolism in the lake is discussed.

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References

  1. Aitchison PA, Butt VS (1973) The relation between the synthesis of inorganic polyphosphate and phosphate uptake byChlorella vulgaris. J Exp Bot 24:497–510

    Google Scholar 

  2. Brock TD (1978) Use of fluorescence microscopy for quantifying phytoplankton, especially filamentous blue-green algae. Limnol Oceanogr 23:158–160

    Google Scholar 

  3. Button DK (1985) Kinetics of nutrient-limited transport and microbial growth. Microbiol Rev 49:270–297

    PubMed  Google Scholar 

  4. Chrost RJ (1978) Extracellular release inChlorella vulgaris culture and the role of bacteria-accompanying algae in this process. Acta Microbiol Polon 27:55–62

    Google Scholar 

  5. Chrost RJ (1984) Use of14C-dissolved organic carbon (RDOC) released by algae as a realistic tracer of heterotrophic activity measurements for aquatic bacteria. Arch Hydrobiol Beih Ergebn Limnol 19:207–214

    Google Scholar 

  6. Chrost RJ, Faust MA (1983) Organic carbon release by phytoplankton: its composition and utilization by bacterioplankton. J Plankton Res 5:477–493

    Google Scholar 

  7. Chrost RJ, Krambeck HJ (1986) Fluorescence correction for measurements of enzyme activity in natural waters using methylumbelliferyl-substrates. Arch Hydrobiol 106:70–90

    Google Scholar 

  8. Chrost RJ, Siuda W, Halemejko GZ (1984) Long-term studies on alkaline phosphatase activity (APA) in a lake with fish-aqua-culture in relation to lake eutrophication and phosphorus cycle. Arch Hydrobiol (Suppl) 70:1–32

    Google Scholar 

  9. Chrost RJ, Siuda W, Albrecht D, Overbeck J (1986) A method for determination of enzymatically hydrolyzable phosphate (EHP) in natural waters. Limnol Oceanogr 32:662–667

    Google Scholar 

  10. Chrost RJ, Wcislo R, Halemejko GZ (1986) Enzymatic decomposition of organic matter by bacteria in eutrophic lake. Arch Hydrobiol 107:145–165

    Google Scholar 

  11. Chu SP (1946) The utilization of organic phosphorus by phytoplankton. J Mar Biol Assoc UK 26:285–295

    Google Scholar 

  12. Cole JJ, Likens GE, Strayer DL (1982) Photosynthetically produced dissolved organic carbon: an important carbon source for planktonic bacteria. Limnol Oceanogr 27:1080–1090

    Google Scholar 

  13. Derenbach JB, Williams PJLeB (1974) Autotrophic and bacterial production: fractionation of plankton populations by differential filtration of samples from the English Channel. Mar Biol 25:263–269

    Article  Google Scholar 

  14. Dillon PJ, Rigler FH (1974) The phosphorus-chlorophyll relationship in lakes. Limnol Oceanogr 19:767–773

    Google Scholar 

  15. Francko DA (1984) Relationship between phosphorus functional classes and alkaline phosphatase activity in reservoir lakes. J Freshwat Ecol 2:541–547

    Google Scholar 

  16. Francko DA, Heath RT (1979) Functionally distinct classes of complex phosphorus compounds in lake water. Limnol Oceanogr 24:463–473

    Google Scholar 

  17. Fuhrman JA, Azam F (1982) Thymidine incorporation as a measure of heterotrophic bacterioplankton production in marine surface waters; evaluation and field results. Mar Biol 66:109–120

    Article  Google Scholar 

  18. Gage MA, Gorham E (1985) Alkaline phosphatase activity and cellular phosphorus as an index of the phosphorus status of phytoplankton in Minnesota lakes. Freshwater Biology 15:227–233

    Google Scholar 

  19. Golterman HL, Clymo RS (1969) Methods for chemical analysis of freshwaters. IBP Handbook No 8, Blackwell Sci Publishers, Oxford

    Google Scholar 

  20. Halemejko GZ, Chrost RJ (1984) The role of phosphatases in phosphorus mineralization during decomposition of lake phytoplankton blooms. Arch Hydrobiol 101:489–502

    Google Scholar 

  21. Healey FP, Hendzel LL (1980) Physiological indicators of nutrient deficiency in lake phytoplankton. Can J Fish Aqua Sci 37:442–453

    Google Scholar 

  22. Heath RT, Cooke GD (1975) The significance of alkaline phosphatase in a eutrophic lake. Int Ver Theor Angew Limnol Verh 19:959–965

    Google Scholar 

  23. Hutchinson GE (1941) Limnological studies in Connecticut. IV. The mechanism of intermediary metabolism in stratified lakes. Ecol Monogr 11:21–60

    Google Scholar 

  24. Jones JG (1972) Studies of freshwater microorganisms: phosphatase activity in lakes of differing degrees of eutrophication. J Ecol 60:777–791

    Google Scholar 

  25. Kobori H, Taga N (1979) Phosphatase activity and its role in the mineralization of organic phosphorus in coastal seawater. J Exp Mar Biol Ecol 36:23–39

    Article  Google Scholar 

  26. Koroleff F (1976) Determination of phosphorus. In: Grasshoff K (ed) Methods of seawater analysis. Verlag Chemie, New York, pp 117–126

    Google Scholar 

  27. Kuenzler EJ (1965) Glucose-6-phosphate utilization by marine algae. J Phycol 1:156–164

    Google Scholar 

  28. Meffert ME, Overbeck J (1979) Regulation of bacterial growth by algal release products. Arch Hydrobiol 87:118–121

    Google Scholar 

  29. Murphy J, Riley JP (1962) A modified single solution method for the determination of phosphate in natural waters. Anal Chim Acta 27:31–36

    Article  Google Scholar 

  30. Perry MJ (1976) Phosphate utilization by an oceanic diatom in phosphorus-limited chemostat culture and in the oligotrophic waters of the Central North Pacific. Limnol Oceanogr 21:88–107

    Google Scholar 

  31. Pettersson K (1980) Alkaline phosphatase activity and algal surplus phosphorus as phosphorus-deficiency indicators in Lake Erken. Arch Hydrobiol 89:54–87

    Google Scholar 

  32. Provasoli L (1958) Nutrition and ecology of protozoa and algae. Annu Rev Microbiol 12:279–308

    Article  PubMed  Google Scholar 

  33. Raven JA (1980) Nutrient transport in microalgae. In: Rose AH, Morris JG (eds) Advances in microbial physiology, vol. 21. Academic Press, San Francisco, pp 48–227

    Google Scholar 

  34. Rhee GY (1972) Competition between an alga and an aquatic bacterium for phosphate. Limnol Oceanogr 17:505–514

    Google Scholar 

  35. Rivkin RB, Swift E (1980) Characterization of alkaline phosphatase and organic phosphorus utilization in the oceanic dinoflagellatePyrocystis noctiluca. Mar Biol 61:1–8

    Article  Google Scholar 

  36. Schindler DW (1977) Evolution of phosphorus limitation in lakes. Science 195:260–262

    Google Scholar 

  37. Smith RE, Kalff J (1981) The effect of phosphorus limitation on algal growth rates: evidence from alkaline phosphatase. Can J Fish Aqua Sci 38:1421–1427

    Google Scholar 

  38. Solorzano L (1978) Soluble fractions of phosphorus compounds and alkaline phosphatase activity in Loch Creran and Loch Etire, Scotland. J Exp Mar Biol Ecol 34:227–232

    Google Scholar 

  39. Stewart AJ, Wetzel RG (1982) Phytoplankton contribution to alkaline phosphatase activity. Arch Hydrobiol 93:265–271

    Google Scholar 

  40. Taft JL, Loftus ME, Taylor WR (1977) Phosphate uptake from phosphomonoesters by phytoplankton in the Chesapeake Bay. Limnol Oceanogr 22:1012–1021

    Google Scholar 

  41. Vincent WV (1981) Rapid physiological assays for nutrient demand by the plankton. II. Phosphorus. J Plankton Res 3:699–710

    Google Scholar 

  42. Wetzel RG (1983) Limnology. Saunders College Publishing, Philadelphia

    Google Scholar 

  43. Wright RT, Hobbie JE (1966) Use of glucose and acetate by bacteria and algae in aquatic ecosystems. Ecology 47:447–464

    Google Scholar 

  44. Wynne D, Berman T (1980) Hot water extractable phosphorus: an indicator of nutritional status ofPeridinium cinctum (Dinophyceae) from Lake Kinneret? J Phycol 16:40–46

    Article  Google Scholar 

  45. Wynne D, Gophen M (1981) Phosphatase activity in freshwater Zooplankton. Oikos 37:369–376

    Google Scholar 

  46. Zimmermann R, Meyer-Reil LA (1974) A new method for fluorescence staining of bacterial population on membrane filters. Kiel Meeresforsch 30:24–28

    Google Scholar 

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Chróst, R.J., Overbeck, J. Kinetics of alkaline phosphatase activity and phosphorus availability for phytoplankton and bacterioplankton in lake plu\see (North German Eutrophic Lake). Microb Ecol 13, 229–248 (1987). https://doi.org/10.1007/BF02025000

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