Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2012 | 21 | 3 |
Tytuł artykułu

Development of microbial biomass and enzyme activities in mine soils

Treść / Zawartość
Warianty tytułu
Języki publikacji
This study assessed the development of microbial biomass, basal respiration, and the activities of dehydrogenase, urease, and acid Phosphomonoesterase in sandy mine soils reclaimed for forestry and those developing under vegetation from natural succession. The mine soils contained significantly less organic C (Corg) and total N (Nt) than the natural forest soils. However, in some of them the microbial biomass and basal respiration attained values typical for the natural forest soils. The content of Nt proved to be the most important control on the microbial biomass, basal respiration, and the activities of dehydrogenase and Phosphomonoesterase in the mine soils. All the microbial properties were positively related also to Corg content. The activities of dehydrogenase and urease depended strongly on microbial biomass (Cmic). Hence, high activities of these enzymes were determined in soils containing high Cmic. The acid Phosphomonoesterase activity was also positively related to Cmic, but its activity was increased in the soils with low P contents.
Słowa kluczowe
Opis fizyczny
  • Department of Open-strip Mining, AGH University of Science and Technology, Mickiewicza 30, 30-059 Krakow, Poland
  • 1. BAUHUS J., KHANNA P.K. The significance of microbial biomass in forest soils. In: N. Rastin, J. Bauhus (Eds.), Going Underground - Ecological Studies in Forest Soils, Research Signpost, Trivandrum, India, pp. 77-110, 1999.
  • 2. HARRIS J.A. Measurements of the soil microbial community for estimating the success of restoration. Eur. J. Soil Sei. 54, 801,2003.
  • 3. NANNIPIERI P., KANDELER E., RUGGIERO P. Enzyme activities and microbiological and biochemical processes in soil. In: Burns RG and Dick RP (Ed.) Enzymes in the environment. Activity, ecology and applications. Marcel Dekker, New York, pp 1-33, 2002.
  • 4. CALDWELL B.A. Enzyme activities as a component of soil biodiversity: a review. Pedobiologia 49, 637, 2005.
  • 5. GIL-SOTRES F., TRASAR-CEPEDA C, LEIRÓS M.C., SEOANE S. Different approaches to evaluating soil quality using biochemical properties. Soil Biol. Biochem. 37, 877, 2005.
  • 6. DE MORA A.P., ORTEGA-CALVO J.J., CABRERA F., MADEJÓN E. Changes in enzyme activities and microbial biomass after "in situ" remediation of a heavy metal-contaminated soil. Appl. Soil Ecol. 28, 125, 2005.
  • 7. BALDRIAN P., TRÖGL J; FROUZ J., ŠNAJDR J., VALÁŠKOVA V., MERAHUTOVÁ V., CAJTHAML T., HERINKOVÁ J. Enzyme activities and microbial biomass in topsoil layer during spontaneous succession in spoil heaps after brown coal mining. Soil Biol. Biochem. 40, 2107., 2008.
  • 8. STRZYSZCZ Z. The soil less reclamation method of the after-industrial areas in Silesian province achievements and threats. Soil Science Annual. 25, 405, 2004 [In Polish],
  • 9. PIETRZYKOWSKI M. Characteristics of selected features of arborescent vegetation in reclaimed areas and in areas left for succession as exemplified by experimental plots in the Szczakowa sand mine excavation. Acta Agr. Silv. ser. Silv., 63, 1,2005 [In Polish],
  • 10. CHODAK M„ PIETRZYKOWSKI M„ NIKLIŃSKA M. Development of microbial properties in a chronosequence of sandy mine soils. Applied Soil. Ecol. 41, 259, 2009.
  • 11. SCHLICHTING E„ BLUME H.O. Bodenkundliches Praktikum. Paul Parey, Hamburg, 1966.
  • 12. ANDERSON J.P.E, DOMSCH K.H. A physiological method for the quantitative measurement of microbial biomass in soils. Soil Biol. Biochem. 10, 215,1978.
  • 13. VON MERSI W. Dehydrogenase activity with the substrate INT. In: Methods in soil biology. Springer-Verlag: Berlin, Heidelberg, pp. 243-245,1996.
  • 14. MARGESIN R. Acid and alkaline Phosphomonoesterase activity with substrate p-nitrophenyl phosphate. In: Methods in soil biology. Springer-Verlag: Berlin, Heidelberg, pp. 213-217, 1996.
  • 15. KANDELER E. Urease activity by colorimetric technique. In: Methods in soil biology. Springer-Verlag: Berlin, Heidelberg, pp. 171-174,1996.
  • 16. FRANZLUEBBERS A.J., HANEY F., HONS F.M., ZUBERER D.A., Active fractions of organic matter in soils with different texture. Soil Biol. Biochem. 28, 1367,1996.
  • 17. MÜLLER T., HÖPER H. Soil organic matter turnover as a function of the soil clay content: consequences for model applications. Soil Biol. Biochem. 36, 877, 2004.
  • 18. SOLLINS P., HOMANN P., CALDWELL B.A. Stabilization and destabilization of soil organic matter: Mechanisms and controls. Geoderma 74, 65,1996.
  • 19. CHODAK M„ NIKLIŃSKA M. Effect of texture and tree species on microbial properties of mine soils. Appl. Soil Ecol. 46, 268, 2010.
  • 20. ŠOURKOVÁ M., FROUZ J., FETTWEIS U., BENS O., HÜTTL R.F., ŠANTRŮČKOVÁ H. Soil development and properties of microbial biomass succession in reclaimed post mining sites near Sokolov (Czech Republic) and near Cottbus (Germany). Geoderma 129, 73, 2005.
  • 21. BOLAN N.S., HEDLEY M.J., WHITE R.E. Processes of soil acidification during nitrogen cycling with emphasis on legume based pastures. Plant Soil 134, 53,1991.
  • 22. ARNOLD G. Soil acidification as caused by the nitrogen uptake pattern of Scots pine (Pinus sylvestris) Plant Soil 142,41,1992.
  • 23. EMMER I.M., SEVINK J. Temporal and vertical changes in the humus form profile during primary succession of Pinus sylvestris. Plant Soil 167, 281, 1994.
  • 24. INSAM H., DOMSCH K.H. Relationships between soil organic carbon and microbial biomass on chronosequence of reclaimed sites. Microb. Ecol. 15, 177,1988.
  • 25. ŠANTRŮČKOVÁ H. Microbial biomass, activity and soil respiration in relation to secondary succession. Pedobiologia 36,314,1992.
  • 26. GRAHAM M.H., HAYNES R.J. Organic matter status and the size, activity and metabolic diversity of the soil microflora as indicators of the success of rehabilitation of sand dunes. Biol. Fertil. Soils 39, 429, 2004.
  • 27. PASCUAL J.A., GARCIA C., HERNANDEZ T., MORENO J.L., ROS M. Soil microbial activity as a biomarker of degradation and remediation processes. Soil Biol. Biochem. 32, 1877, 2000.
  • 28. TAN X., CHANG S.X., KABZEMS R. Soil compaction and forest floor removal reduced microbial biomass and enzyme activities in a boreal aspen forest soil. Biol. Fertil. Soils 44, 471,2008.
  • 29. SINSABAUGH R.L., ANTIBUS R.K., LINKINS A.E., MCCLAUGHERTY C.A., RAYBURN L., REPERT D„ WEILAND T. Wood decomposition: nitrogen and phosphorus dynamics in relation to extracellular enzyme activity. Ecology 74, 1586, 1993.
  • 30. ALLISON V.J., CONDRON L.M., PELTZER D.A., RICHARDSON S.J., TURNER B.L. Changes in enzyme activities and soil microbial community composition along carbon and nutrient gradients at the Franz Josef chronosequence, New Zealand. Soil Biol. Biochem. 39, 1770, 2007.
  • 31. ŠANTRŮČKOVÁ H., VRBA J., PICEK, T., KOPACEK. Soil biochemical activity and phosphorus transformations and losses from acidified forest soils. Soil Biol. Biochem. 36, 1569, 2004.
  • 32. SELTMANS P.C., HART S.C., BOYLE S.I., STARK J.M. Red alder (Alnus rubra) alters community-level microbial function in conifer forests of the Pacific Northwest, USA. Soil Biol. Biochem. 37, 1860, 2005.
  • 33. ALLISON S.D., VITOUSEK P.M. Responses of extracellular enzymes to simple and complex nutrient inputs. Soil Biol. Biochem. 37, 937, 2005.
  • 34. PRIHA O., SMOLANDER A. Nitrogen transformations in soil under Pinus sylvestris, Picea abies and Betula pendula at two forest sites. Soil Biol. Biochem. 31, 965,1999.
  • 35. ANDERSSON S., NILSSON S.I. Influence of pH and temperature on microbial activity, substrate availability of soil solution bacteria and leaching of dissolved organic carbon in a mor humus. Soil Biol. Biochem. 33, 1181, 2001.
  • 36. QUILCHAO C., MARAŃÓN T. Dehydrogenase activity in Mediterranean forest soils. Biol. Fertil. Soils 35, 102, 2002.
Typ dokumentu
Identyfikator YADDA
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.