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Effects of plant-bacterial-amoebal interactions on plant uptake of nitrogen under field conditions

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Summary

Bacterial biomass and numbers of bacterivorous naked amoebae were estimated daily in soil associated with barley roots and, to avoid the influence of roots, in soil from a field in its fifth summer under bare fallow. The estimates were associated with two rainfall events and were started just before the first. Increases in bacteria were observed after each rainfall, and bacterial production was about the same size for both treatments. A peak in naked amoebae followed each burst of bacterial production in the root-associated soil, whereas in the fallowed soil protozoan production was low after the first rainfall and undetectable after the second. The bacterial populations in the fallowed soil had yet to decline by the end of the 12-day study, probably because grazing pressure by protozoa was low. Calculations based (1) on short-term decreases in bacterial biomass in soil close to roots or (2) on the amount of C added to the soil by plants over the growing season indicated that N released via bacterial-protozoan interactions contributed 10%–17% of the N taken up by the fertilized barley.

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References

  • Andrén O (1987) Decomposition of shoot and root litter of barley, lucerne and meadow fescue under field conditions. Swed J Agric Res 17:113–122

    Google Scholar 

  • Bamforth SS (1976) Rhizosphere-soil microbial comparisons in subtropical forests of southeastern Louisiana. Trans Am Microsc Soc 95:613–621

    Google Scholar 

  • Bergström L (1986) Distribution and temporal changes of mineral nitrogen in soils supporting annual and perennial crops. Swed J Agric Res 16:105–112

    Google Scholar 

  • Burnbanck WD (1942) Physiology of the ciliate Colpidium colpoda: I. The effect of various bacteria as food on the division rate of Colpidium colpoda. Physiol Zool 15:342–362

    Google Scholar 

  • Clarholm M (1981) Protozoan grazing of bacteria in soil — impact and importance. Microb Ecol 7:343–350

    Google Scholar 

  • Clarholm M (1985a) Interactions of bacteria, protozoa and plants leading to mineralization of soil nitrogen. Soil Biol Biochem 17:181–187

    Google Scholar 

  • Clarholm M (1985b) Possible roles for roots, bacteria, protozoa and fungi in supplying nitrogen to plants. In: Fitter AH, Atkinson D, Read DJ, Usher MB (eds) Ecological interactions in the soil. Spec Publ No 4, Br Ecol Soc, Blackwell, Oxford, pp 355–365

    Google Scholar 

  • Clarholm M, Rosswall T (1980) Biomass and turnover of bacteria in a forest soil and a peat. Soil Biol Biochem 12:49–57

    Google Scholar 

  • Cox WJ, Reisenauer HM (1973) Growth and ion uptake by wheat supplied nitrogen as nitrate or ammonium or both. Plant and Soil 38:363–380

    Google Scholar 

  • Cutler DW, Crump LM, Sandon H (1922) A quantitative investigation of the bacterial and protozoan population of the soil, with an account of the protozoan fauna. Phil Trans R Soc B 211:317–350

    Google Scholar 

  • Darbyshire JF, Greaves MP (1967) Bacteria and protozoa in the rhizosphere of Sinapis alba L., Trifolium repens L. and Lolium perenne L. Can J Microbiol 13:1057–1068

    Google Scholar 

  • Darbyshire JF, Wheatley RF, Greaves MP, Inkson RHE (1974) A rapid micromethod for estimating bacterial and protozoan populations in soil. Rev Ecol Biol Soil 11:465–474

    Google Scholar 

  • Dive D (1973) La nutrition holozoique des protozoaires ciliés: Ses conséquences dans l'épuration naturelle et artificielle. Ann Biol 12:343–380

    Google Scholar 

  • Elliott ET, Coleman DC (1977) Soil protozoan dynamics in a shortgrass prairie. Soil Biol Biochem 9:113–118

    Google Scholar 

  • Elliott ET, Coleman DC, Ingham RE, Trofymow JA (1984a) Carbon and energy flow through microflora and microfauna in the soil subsystem of terrestrial ecosystems. In: Klug MJ, Reddy CA (eds) Current perspectives in microbial ecology. Am Soc Microbiol, Washington DC, pp 424–433

    Google Scholar 

  • Elliott ET, Horton K, Moore JC, Coleman DC, Cole CV (1984b) Mineralization dynamics in fallow dryland wheat plots, Colorado. Plant and Soil 76:149–155

    Google Scholar 

  • FAO-UNESCO (1974) Soil map of the world, vol 1. Geneva, FAOUNESCO

    Google Scholar 

  • Fenchel T (1982) Ecology of heterotrophic microflagellates: 11. Bioenergetics and growth. Mar Ecol Prog Ser 8:225–231

    Google Scholar 

  • Fenchel T (1987) Ecology of protozoa. Brock/Springer Series in contemporary bioscience, Berlin Heidelberg New York

    Google Scholar 

  • Fenchel T, Blackburn TH (1979) Bacteria and mineral cycling. Academic Press, New York London

    Google Scholar 

  • Goldman JC, Caron DA, Andersen DK, Dennett MR (1985) Nutrient cycling in microflagellate food chains: I. Nitrogen dynamics. Mar Ecol Prog Set 24:231–242

    Google Scholar 

  • Haider K, Mosier A, Heinemeyer O (1987) The effect of growing plants on denitrification at high nitrate concentrations. Soil Sci Soc Am J 51:97–102

    Google Scholar 

  • Hansson A-C, Pettersson R, Paustian K (1987) Shoot and root production and nitrogen uptake in barley with and without nitrogen fertilization. Z Acker/Pflanzenbau 158:163–171

    Google Scholar 

  • Hunt HW Coleman DC, Ingham ER, Ingham RE, Elliott ET, Moore JC, Rose SL, Reid CPP, Morley CR (1987) The detrital food web in a shortgrass prairie. Biol Fertil Soils 3:57–68

    Google Scholar 

  • Lucas MI, Probyn TA, Painting SJ (1987) An experimental study of microflagellate bacterivory: Further evidence for the importance and complexity of microplanctonic interactions. S Aft J Mar Sci 5:791–808

    Google Scholar 

  • Page FC (1967) Taxonomic criteria for limax amoebae with description of 3 new species of Hartmannella and 3 of Valkampfia. J Protozool 14:499–521

    Google Scholar 

  • Paustian K, Andrén O, Bostrom U, Clarholm M, Hansson A-C, Johansson G, Lindberg T, Pettersson R, Sohlenius B (1989) Carbon and nitrogen budgets for four agroecosystems with annual and perennial crops with and without fertilization. J Appl Ecol (in press)

  • Pettersson R (1989) Above-ground growth dynamics and net production of spring barley in relation to nitrogen fertilization. Swed J Agric Res (in press)

  • Schnürer J, Clarholm M, Bostrom S, Rosswall T (1986a) Effects of moisture on soil organisms and nematodes: A field experiment. Microb Ecol 12:217–230

    Google Scholar 

  • Schnürer J, Clarholm M, Rosswall T (1986b) Fungi, bacteria and protozoa in soil from four arable cropping systems. Biol Fertil Soils 2:119–126

    Google Scholar 

  • Singh BN (1941 a) Selectivity in bacterial food by soil amoebae in pure and mixed cultures and in sterilized soil. Ann Appl Biol 28:52–64

    Google Scholar 

  • Singh BN (194l b) The influence of different bacterial food supplies on the rate of reproduction of Colpoda steinii, and the factors influencing encystation. Ann Appl Biol 28:65–73

    Google Scholar 

  • Steen E, Jansson PE, Persson J (1984) Experimental site of the ‘Ecology of Arable Land’ project. Acta Agric Scand 34:153–166

    Google Scholar 

  • Van Veen JA, Ladd JN, Frissel MJ (1984) Modelling C and N turnover through the microbial biomass in soil. Plant and Soil 76:257–274

    Google Scholar 

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Clarholm, M. Effects of plant-bacterial-amoebal interactions on plant uptake of nitrogen under field conditions. Biol Fert Soils 8, 373–378 (1989). https://doi.org/10.1007/BF00263171

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  • DOI: https://doi.org/10.1007/BF00263171

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