Plant and Soil

, Volume 290, Issue 1–2, pp 269–282 | Cite as

Increase in pH stimulates mineralization of ‘native’ organic carbon and nitrogen in naturally salt-affected sandy soils

  • Xiao-gang Li
  • Zed Rengel
  • Emmanuel Mapfumo
  • Bhupinderpal-Singh
Original Paper

Abstract

Large amounts of terrestrial organic C and N reserves lie in salt-affected environments, and their dynamics are not well understood. This study was conducted to investigate how the contents and dynamics of ‘native’ organic C and N in sandy soils under different plant species found in a salt-affected ecosystem were related to salinity and pH. Increasing soil pH was associated with significant decreases in total soil organic C and C/N ratio; particulate (0.05–2 mm) organic C, N and C/N; and the C/N ratio in mineral-associated (<0.05 mm) fraction. In addition, mineral-associated organic C and N significantly increased with an increase in clay content of sandy soils. During 90-day incubation, total CO2-C production per unit of soil organic C was dependent on pH [CO2-C production (g kg−1 organic C) = 22.5 pH – 119, R 2 = 0.79]. Similarly, increased pH was associated with increased release of mineral N from soils during 10-day incubation. Soil microbial biomass C and N were also positively related to pH. Metabolic quotient increased with an increase in soil pH, suggesting that increasing alkalinity in the salt-affected soil favoured the survival of a bacterial-dominated microbial community with low assimilation efficiency of organic C. As a result, increased CO2-C and mineral N were produced in alkaline saline soils (pH up to 10.0). This pH-stimulated mineralization of organic C and N mainly occurred in particulate but not in mineral-associated organic matter fractions. Our findings imply that, in addition to decreased plant productivity and the litter input, pH-stimulated mineralization of organic matter would also be responsible for a decreased amount of organic matter in alkaline salt-affected sandy soils.

Keywords

Global C balance Microbial activity Microbial biomass Particulate organic matter pH Salinity 

Notes

Acknowledgments

We would like to thank Kosta Voltchanski and Rolf Polsen for their assistance with collection of soil samples. The Department of Conservation and Land Management (CALM) provided some historical and geological information on the study site. We especially thank Michael Smirk and Paul Damon for their assistances with the laboratory analyses.

References

  1. Agarwal AS, Singh BR, Kanehiro Y (1971) Ionic effect of salts on mineral nitrogen release in an allophonic soil. Soil Sci Soc Am Proc 35:454–457CrossRefGoogle Scholar
  2. Beltrán-Hernández RI, Coss-Muňoz E, Luna-Guido ML, Mercado-García F, Siebe C, Dendooven L (1999) Carbon and nitrogen dynamics in alkaline saline soil of the former Lake Texcoco (Mexico) as affected by application of sewage sludge. Eur J Soil Sci 50:601–608CrossRefGoogle Scholar
  3. Blakemore LC, Searle PL, Daly DK (1987) Methods for chemical analysis of soils. N Z, Soil Bur Sci Rep., 80 ppGoogle Scholar
  4. Broadbent FE, Nakashima T (1971) Effect of added salts on nitrogen mineralization in three California soils. Soil Sci Soc Am Proc 35:457–460CrossRefGoogle Scholar
  5. Chandra S, Joshi HC, Pathak H, Jain MC, Kalra N (2002) Effect of potassium salts and distillery effluent on carbon mineralization. Bioresour Technol 83:255–257PubMedCrossRefGoogle Scholar
  6. Chen G., Zhu H, Zhang Y (2003) Soil microbial activities and carbon and nitrogen fixation. Res Microbiol 154:393–398PubMedCrossRefGoogle Scholar
  7. Craine JM, Tilman D, Wedin D, Reich P, Tjoelker M, Knops J (2002) Functional traits, productivity and effects on nitrogen cycling of 33 grassland species. Funct Ecol 16:63–574CrossRefGoogle Scholar
  8. Crowley DE, Alvey SA (2002) Regulation of microbial processes by soil pH. In: Rengel Z (ed) Handbook of plant growth. pH as the master variable. Marcel Dekker, Inc, New York, USA, pp 351–382Google Scholar
  9. Dalal RC, Wang W, Robertson GP, Parton WJ (2003) Nitrous oxide emission from Australian agricultural lands and mitigation options: a review. Aust J Soil Res 41:165–195CrossRefGoogle Scholar
  10. Domènech R, Vilà M, Gesti J, Serrasolses I (2006) Neighbourhood association of Cortaderia selloana invasion, soil properties and plant community structure in Mediterranean coastal grasslands. Acta Oecol 29:171–177CrossRefGoogle Scholar
  11. Heilman P (1975) Effect of added salts on nitrogen release and nitrate levels in forest soils of the Washington coastal area. Soil Sci Soc Am Proc 39:778–782CrossRefGoogle Scholar
  12. Gee GW, Bauder JW (1986) Particle size analysis. In: Klute A (ed) Methods of soil analysis, Part 1. Physical and mineralogical methods. American Society of Agronomy, Inc., Madison, Wisconsin, USA, pp 383–411Google Scholar
  13. Joergensen RG, Brookes PC (1990) Ninhydrin-reactive nitrogen measurements of microbial biomass in 0.5 M K2SO4 soil extracts. Soil Biol Biochem 22:1023–1027CrossRefGoogle Scholar
  14. Kemmitt SJ, Wright D, Goulding KW T, Jones DL (2006) pH regulation of carbon and nitrogen dynamics in two agricultural soils. Soil Biol Biochem 38:898–911CrossRefGoogle Scholar
  15. Kempers AJ, Luft AG (1988) Re-examination of the determination of environmental nitrate as nitrite by reduction with hydrazine. Analyst 113:1117–1120PubMedCrossRefGoogle Scholar
  16. Khalil MI, Hossain MB, Schmidhalter U (2005) Carbon and nitrogen mineralization in different upland soils of the subtropics treated with organic materials. Soil Biol. Biochem 37:1507–1518CrossRefGoogle Scholar
  17. Kimble J, Cook T, Eswaran H (1990) Organic carbon on a volume basis in tropical and temperate soils. Transactions of the 14th International Congress of Soil Science, Kyoto, pp V248–V253Google Scholar
  18. Kinnear PR, Gray CD (2000) SPSS for Windows made simple: release 10. Psychology Press, Hove, UKGoogle Scholar
  19. Konukcu F, Gowing JW, Rose DA (2006) Dry drainage: a sustainable solution to waterlogging and salinity problems in irrigation areas. Agr Water Manag 83:1–12CrossRefGoogle Scholar
  20. Laura RD (1974) Effects of neutral salts on C and N mineralization of organic matter in soil. Plant Soil 41:113–127CrossRefGoogle Scholar
  21. Laura RD (1976) Effects of alkali salts on C and N mineralization of organic matter in soil. Plant Soil 44:587–596CrossRefGoogle Scholar
  22. Lemenih M, Itanna F (2004) Soil carbon stocks and turnovers in various vegetation types and arable lands along an elevation gradient in southern Ethiopia. Geoderma 123:177–188CrossRefGoogle Scholar
  23. Li X, Li F, Bhupinderpal-Singh, Cui Z, Rengel Z (2006a) Decomposition of maize straw in saline soil. Biol Fertil Soils 42:366–370CrossRefGoogle Scholar
  24. Li X, Li F, Ma Q, Cui Z (2006b) Interactions of NaCl and Na2SO4 on soil organic carbon mineralization after addition of maize straws. Soil Biol Biochem 38:2328–2335CrossRefGoogle Scholar
  25. Luna-Guido ML, Beltran-Hernandez RI, Dendooven L (2001) Dynamics of 14C-labelled glucose in alkaline saline soil. Soil Biol Biochem 33:707–719CrossRefGoogle Scholar
  26. Midwood AJ, Boutton TW (1998) Soil carbonate decomposition by acid has little effect on δ13 C organic matter. Soil Biol Biochem 30:1301–1307CrossRefGoogle Scholar
  27. Motavalli PP, Palm CA, Parton WJ, Elliott ET, Frey SD (1995) Soil pH and organic C dynamics in tropical forest soils: evidence from laboratory and simulation studies. Soil Biol Biochem 27:1589–1599CrossRefGoogle Scholar
  28. Nelson PN, Ladd JN, Oades JM (1996) Decomposition of 14C-labelled plant material in a salt-affected soil. Soil Biol Biochem 28:433–441CrossRefGoogle Scholar
  29. Nelson PN, Rahman BA, Oades JM (1997) Sodicity and clay type: influence on decomposition of added organic matter. Soil Sci Soc Am J 61:1052–1057CrossRefGoogle Scholar
  30. Niknam SR, McComb J (2000) Salt tolerance screening of selected Australian woody species – a review. Forest Ecol Manage 139:1–19CrossRefGoogle Scholar
  31. Oren A (2001) The bioenergetic basis for the decrease in metabolic diversity at increasing salt concentrations: implications for the functioning of salt lake ecosystems. Hydrobiologia 466:61–72CrossRefGoogle Scholar
  32. Ormeño E, Baldy V, Ballini C, Larchevêque M, Périssol C, Fernandez C (2006) Effects of environmental factors and leaf chemistry on leaf litter colonization by fungi in a Mediterranean shrubland. Pedobiologia 50:1–10Google Scholar
  33. Pankhurst CE, Yu S, Hawke BG., Harch BD (2001) Capacity of fatty acid profiles and substrate utilization patterns to describe differences in soil microbial communities associated with increased salinity or alkalinity at three locations in South Australia. Biol. Fertil Soils 33:204–217CrossRefGoogle Scholar
  34. Pannell DJ, Ewing MA (2006) Managing secondary dryland salinity: options and challenges. Agric Water Manage 80:41–56CrossRefGoogle Scholar
  35. Pathak H, Rao LN (1998) Carbon and nitrogen mineralization from added organic matter in saline and alkali soils. Soil Biol Biochem 30:695–702CrossRefGoogle Scholar
  36. Rayment GE, Higginson FR (1992) Australian laboratory handbook of soil and water chemical methods. Inkata Press, pp 172–177Google Scholar
  37. Rengel Z (2002) Role of pH in availability of ions in soil. In: Rengel Z (ed) Handbook of plant growth. pH as the master variable. Marcel Dekker, Inc, New York, USA, pp 323–350Google Scholar
  38. Rietz DN, Haynes RJ (2003) Effects of irrigation-induced salinity and sodicity on soil microbial activity. Soil Biol Biochem 35:845–854CrossRefGoogle Scholar
  39. Robson AD (1989) Soil acidity and plant growth. Academic Press, SydneyGoogle Scholar
  40. Ruiz-Jaén MC, Aide TM (2005) Vegetation structure, species diversity, and ecosystem processes as measures of restoration success. Forest Ecol Manage 218:1591–1573Google Scholar
  41. Sarig S, Emily BR, Mary KF 1993 Microbial activity-soil structure: response to saline water irrigation. Soil Biol Biochem 25:693–697CrossRefGoogle Scholar
  42. Searle PL (1984) The Berthelot or indophenol reaction and its use in the analytical chemistry of nitrogen. Analyst 109:549–568CrossRefGoogle Scholar
  43. Semmartin M, Ghersa CM (2006) Intraspecific changes in plant morphology, associated with grazing, and effects on litter quality, carbon and nutrient dynamics during decomposition. Aust Ecol 31:99–105CrossRefGoogle Scholar
  44. Spain AV (1990) Influence of environmental conditions and some soil chemical properties on the carbon and nitrogen contents of some tropical Australia rainforest soils. Aust J Soil Res 28:825–839CrossRefGoogle Scholar
  45. Sparling G., Zhu C (1993) Evaluation and calibration of biochemical methods to measure microbial biomass C and N in soils from Western Australia. Soil Biol Biochem 25:1793–1801CrossRefGoogle Scholar
  46. Szabolcs I (1989) Salt-affected soils. CRC Press, Inc, Boca Raton, FloridaGoogle Scholar
  47. Ventosa A, Nieto JJ, Oren A (1998) Biology of moderately halophilic aerobic bacteria. Microbiol Mol Biol R 62:504–544Google Scholar
  48. Wardle DA, Ghani A (1995) A critique of the microbial metabolic quotient (qCO2) as a bioindicator of disturbance and ecosystem development. Soil Biol Biochem 27:1601–1610CrossRefGoogle Scholar
  49. Wedin DA, Tilman D (1990) Species effects on nitrogen cycling: a test with perennial grasses. Oecologia 84:433–441Google Scholar

Copyright information

© Springer Science+Business Media B.V. 2006

Authors and Affiliations

  • Xiao-gang Li
    • 1
    • 2
  • Zed Rengel
    • 2
  • Emmanuel Mapfumo
    • 2
  • Bhupinderpal-Singh
    • 2
  1. 1.Department of Resources and Environmental SciencesGansu Agricultural UniversityLanzhouChina
  2. 2.School of Earth and Geographical SciencesThe University of Western AustraliaCrawleyAustralia

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