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Zooplankton induced changes in dissolved free amino acids and in production rates of freshwater bacteria

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Abstract

This study examined the importance of zooplankton in the flux of dissolved free amino acids (DFAA) in the water and into bacteria. DFAA release rates were followed in laboratory grazing experiments usingDaphnia galeata andEudiaptomus graciloides as grazers, andScenedesmus acutus andSynechococcus elongatus as food sources. Except for minor initial peaks, DFAAs were released continuously during the first 2 hours and made up 6–12% (in one experiment 50%) of the calculated ingestion rates. During three diel studies in lakes, effects of removal and increase of the density of zooplankton (>200μm) on the pools of DFAA as well as on the bacterial production were followed. During two of the diel studies, higher DFAA pools were measured when 3–4 times the natural zooplankton density was present, and in one study a minor increase also occurred in the bacterial production, compared with results from experiments without zooplankton and with a natural zooplankton density. The increase in bacterial growth coincided with a decline in DFAA. During the third study, neither DFAA nor the bacterial production changed significantly when the zooplankton density was increased 3 times. Removal of zooplankton, however, caused a decline in both DFAA and bacterial production. Our data suggest a close relationship between occurrence of zooplankton and release of DFAA, but the factors regulating the amount of DFAA released and its effect on bacterial growth are not yet understood.

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References

  1. Copping AE, Lorenzen CJ (1980) Carbon budget of a marine phytoplankton-herbivore system with carbon-14 as a tracer. Limnol Oceanogr 25:873–882

    Google Scholar 

  2. Crisman TL, Beaver JR, Bays JS (1981) Examination of the relative impact of microzooplankton and macrozooplankton on bacteria in Florida lakes. Verh Int Verein Limnol 21:359–362

    Google Scholar 

  3. Eppley RW, Horrigan SG, Fuhrman JA, Brooks ER, Price CC, Sellner K (1981) Origins of dissolved organic matter in Southern California coastal waters: experiments on the role of zooplankton. Mar Ecol Prog Ser 6:149–159

    Google Scholar 

  4. Fuhrman JA, Azam F (1980) Bacterioplankton secondary production estimates for coastal waters of British Columbia, Antarctica, and California. Appl Environ Microbiol 39:1085–1095

    Google Scholar 

  5. 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

    Google Scholar 

  6. Fuhrman JA, Ammerman JW, Azam F (1980) Bacterioplankton in the coastal euphotic zone: distribution, activity, and possible relationships with phytoplankton. Mar Biol 60:201–207

    Google Scholar 

  7. Gardner WS, Miller WH III (1981) Intracellular composition and net release rates of free amino acids inDaphnia magna. Can J Fish Aquat Sci 38:157–162

    Google Scholar 

  8. Gauld DT (1957) Diurnal variations in the grazing of planktonic copepods. J Mar Biol Ass UK 31:461–474

    Google Scholar 

  9. Hobbie JE, Daley RJ, Jasper S (1977) Use of nuclepore filters for counting bacteria by fluorescence microscopy. Appl Environ Microbiol 33:1225–1228

    PubMed  Google Scholar 

  10. Iturriaga R (1981) Phytoplankton photoassimilated extracellular products: heterotrophic utilization in marine environments. Kiel Meeresforsch Sonderh 5:318–324

    Google Scholar 

  11. Jensen LM, Jørgensen NOG, Søndergaard M (1984) Specific activity. Significance in estimating release rates of extracellular dissolved organic carbon (EOC) by algae. Verh Int Verein Limnol 22:2893–2897

    Google Scholar 

  12. Jørgensen CB (1983) Patterns of uptake of dissolved amino acids in mussels (Mytilus edulis). Mar Biol 73:177–182

    Google Scholar 

  13. Jørgensen NOG (1984) Occurrence and heterotrophic turnover of dissolved free amino acids in the thermically stratified Lake Almind. Verh Int Verein Limnol 22:785–789

    Google Scholar 

  14. Jørgensen NOG, Kristensen E (1980) Uptake of amino acids by three species ofNereis (Annelida: Polychaeta). I. Transport kinetics and net uptake from natural concentrations. Mar Ecol Prog Ser 3:329–340

    Google Scholar 

  15. Jørgensen NOG, Blackburn TH, Henriksen K, Bay D (1981) The importance ofPosidonia oceanica andCymodecea nodosa as contributors of free amino acids in water and sediments of seagrass beds P S Z N I. Mar Ecol 2:97–112

    Google Scholar 

  16. Jørgensen NOG, Søndergaard M, Hansen HJ, Bosselmann S, Riemann B (1983) Diel variation in concentration, assimilation and respiration of dissolved free amino acids in relation to planktonic primary and secondary production in two eutrophic lakes. Hydrobiologia 107:107–122

    Google Scholar 

  17. Lampert W (1978) Release of dissolved organic carbon by grazing zooplankton. Limnol Oceanogr 23:831–834

    Google Scholar 

  18. Lampert W, Taylor BE (1985) Zooplankton grazing in a eutrophic lake: implications of diel vertical migration. Ecology 66:68–82

    Google Scholar 

  19. Lee C, Cronin C (1982) The vertical flux of particulate organic nitrogen in the sea: decomposition of amino acids in the Peru upwelling area and in equatorial Atlantic. J Mar Res 40:227–251

    Google Scholar 

  20. Lehninger AL (1972) Biochemistry. Worth Publication Inc, New York, 833 pp

    Google Scholar 

  21. Lindroth P, Mopper K (1979) High performance liquid chromatography determination of subpicomole amounts of amino acids by precolumn fluorescence derivatization with o-phthaldialdehyde. Anal Chem 51:1667–1674

    Google Scholar 

  22. Mague TH, Friberg E, Hughes DY, Morris I (1980) Extracellular release of carbon by marine phytoplankton: a physiological approach. Limnol Oceanogr 25:262–279

    Google Scholar 

  23. Mopper K, Lindroth P (1982) Diel and depth variations in dissolved free amino acids and ammonium in the Baltic Sea determined by shipboard HPLC analyses. Limnol Oceanogr 27:336–347

    Google Scholar 

  24. Paffenhöfer GA, Strickland JDH (1970) A note on the feeding ofCalanus helgolandicus on detritus. Mar Biol 5:97–99

    Google Scholar 

  25. Parsons TR, Stephens K, Strickland JDH (1961) On the chemical composition of eleven species of marine phytoplankters. J Fish Res Bd Can 18:1001–1016

    Google Scholar 

  26. Pedrós-Alió C, Brock TD (1982) Assessing biomass and production of bacteria in eutrophic Lake Mendota, Wisconsin. Appl Environ Microbiol 44:203–218

    Google Scholar 

  27. Peters RH (1984) Methods for the study of feeding, grazing and assimilation by zooplankton. In: Downing JA, Rigler FH (eds) A manual on methods for the assessment of secondary productivity in fresh waters. IBP Handbook 17, 2nd ed, pp 336–412

  28. Riemann B (1978) Absorption coefficients for chlorophylls a and b in methanol and a comment on interference of chlorophyll b in the determination of chlorophyll a. Vatten 3:187–194

    Google Scholar 

  29. Riemann B (1983) Biomass and production of phyto- and bacterioplankton in eutrophic Lake Tystrup, Denmark. Freshw Biol 13:389–398

    Google Scholar 

  30. Riemann B, Ernst D (1982) Extraction of chlorophylls a and b from phytoplankton using standard extraction techniques. Freshw Biol 12:217–223

    Google Scholar 

  31. Riemann B, Fuhrman JA, Azam F (1982) Bacterial secondary production in freshwater measured by3H-thymidine incorporation method. Microb Ecol 8:101–114

    Google Scholar 

  32. Riemann B, Mathiesen H (1977) Danish research into phytoplankton primary production. Folia Limnol Scand 17:49–54

    Google Scholar 

  33. Riemann B, Søndergaard M (1984) Measurements of diel rates of bacterial secondary production in aquatic environments. Appl Environ Microbiol 47:632–638

    Google Scholar 

  34. Søndergaard M, Riemann B, Jørgensen NOG (1985) Extracellular organic carbon (EOC) released by phytoplankton and bacterial production. Oikos 45:323–332

    Google Scholar 

  35. Watson SW, Novitsky TJ, Quinby HL, Valois FW (1977) Determination of bacterial number and biomass in the marine environment. Appl Environ Microbiol 33:940–946

    PubMed  Google Scholar 

  36. Webb KL, Johannes RE (1967) Studies of the release of dissolved free amino acids by marine zooplankton. Limnol Oceanogr 12:376–382

    Google Scholar 

  37. Williams PJLeB, Yentsch CS (1976) An examination of photosynthetic production, excretion of photosynthetic products, and heterotrophic utilization of dissolved organic compounds with reference to results from a coastal subtropical sea. Mar Biol 35:31–40

    Google Scholar 

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Riemann, B., Jørgensen, N.O.G., Lampert, W. et al. Zooplankton induced changes in dissolved free amino acids and in production rates of freshwater bacteria. Microb Ecol 12, 247–258 (1986). https://doi.org/10.1007/BF02011168

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