Relationships between soil pH and microbial properties in a UK arable soil

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Abstract

Effects of changing pH along a natural continuous gradient of a UK silty-loam soil were investigated. The site was a 200 m soil transect of the Hoosfield acid strip (Rothamsted Research, UK) which has grown continuous barley for more than 100 years. This experiment provides a remarkably uniform soil pH gradient, ranging from about pH 8.3 to 3.7. Soil total and organic C and the ratio: (soil organic C)/(soil total N) decreased due to decreasing plant C inputs as the soil pH declined. As expected, the CaCO3 concentration was greatest at very high pH values (pH > 7.5). In contrast, extractable Al concentrations increased linearly (R2 = 0.94, p < 0.001) from below about pH 5.4, while extractable Mn concentrations were largest at pH 4.4 and decreased at lower pHs. Biomass C and biomass ninhydrin-N were greatest above pH 7. There were statistically significant relationships between soil pH and biomass C (R2 = 0.80, p < 0.001), biomass ninhydrin-N (R2 = 0.90, p < 0.001), organic C (R2 = 0.83, p < 0.001) and total N (R2 = 0.83, p < 0.001), confirming the importance of soil organic matter and pH in stimulating microbial biomass growth. Soil CO2 evolution increased as pH increased (R2 = 0.97, p < 0.001). In contrast, the respiratory quotient (qCO2) had the greatest values at either end of the pH range. This is almost certainly a response to stress caused by the low p. At the highest pH, both abiotic (from CaCO3) and biotic Co2 will be involved so the effects of high pH on biomass activity are confounded. Microbial biomass and microbial activity tended to stabilise at pH values between about 5 and 7 because the differences in organic C, total N and Al concentrations within this pH range were small. This work has established clear relationships between microbial biomass and microbial activity over an extremely wide soil pH range and within a single soil type. In contrast, most other studies have used soils of both different pH and soil type to make similar comparisons. In the latter case, the effects of soil pH on microbial properties are confounded with effects of different soil types, vegetation cover and local climatic conditions.

Introduction

Soil pH affects all chemical, physical and biological soil properties (Brady and Weil, 2002). The effect of soil pH on specified micro-organisms, on soil microbial biomass, microbial activity and, more recently, on microbial community structure, have been investigated previously. Wardle (1992) concluded that soil pH is probably at least as important as soil C and N concentrations in influencing the size of the microbial biomass. Soil pH also affects organic C solubility (Andersson et al., 2000) and increases the availability of biologically toxic Al with decreasing pH (Flis et al., 1993). This, in turn, affects microbial community structure (e.g. Anderson, 1998, Zelles, 1999, Marstorp et al., 2000) and changes in microbial activity (Bååth and Anderson, 2003).

Some researchers have studied soils with natural pH differences (Anderson and Joergensen, 1997). Others have studied soils in which the pH was changed through anthropogenic intervention, e.g. liming, ash application, alkaline or acidifying pollution (e.g. Anderson, 1998, Thirukkumaran and Parkinson, 2000, Chagnon et al., 2001). Such changes may be short term. Thus, Kemmitt et al. (2005) acidified grassland and arable field plots and showed that the resulting acidification lowered nitrate in the grassland plots in both winter and spring and in cereal plots in spring only during the next 2 years.

Most studies on the effects of soil pH on microbial processes have focused on forest soils (Bååth et al., 1992, Bååth et al., 1995, Frostegård et al., 1993, Blagodatskaya and Anderson, 1998, Pennanen, 2001, Bååth and Anderson, 2003). Less work has been done on arable, grassland or other soils (Bardgett et al., 2001, Arao, 1999, Schutter and Fuhrmann, 2001). In most of the above, variations in soil pH were usually produced by applications of lime or burnt coniferous residues to different soils (Frostegård et al., 1993, Bååth et al., 1995), coal fly ash addition on field plots (Schutter and Fuhrmann, 2001), or industrial pollution with alkaline dust (Bååth et al., 1992).

In other investigations, variations in soil pH were natural, due to chemical characteristics of different types of soils (Blagodatskaya and Anderson, 1998, Arao, 1999, Pennanen, 2001, Bååth and Anderson, 2003). These different studies have demonstrated that soil pH and substrate availability are important factors in determining soil microbial activities. However, the confounding effects of soil type and varying managements remain.

Here, we report the effects of changing soil pH on soil microbial biomass and microbial activity in soils from the Hoosfield acid strip, one of the long term (or Classical) arable field experiments at Rothamsted Research, UK. The Hoosfield acid strip is a perfect site to carry out this investigation. It has an extremely uniform pH gradient (range about 8.3–3.7) along a single soil type, as a result of chalk applied unevenly in the 19th century. It therefore probably is the oldest artificially produced pH gradient in the world.

Section snippets

Soils, sampling and preparation

The soil of Hoosfield, at Rothamsted Research, U.K. is classified as Typic Paleudalf (U.S.D.A., 1992) or Chromic Luvisol (F.A.O., 1989). Such soils were originally acidic, well-drained to moderately well-drained and developed in a relatively silty (loess-containing) superficial deposit overlaying, and mixed with, clay-with-flints. The topsoil is a flinty, silty clay loam (18–27% clay).

Hoosfield has been under arable management since before the 19th century. It probably received only a single

Soil chemical properties along the Hoosfield pH gradient

Soils of the Hoosfield acid strip range from pH 8.3 to 3.7. There does not appear to be, in the literature, any other pH gradient of such a remarkably smooth pH change within the same soil type (Fig. 1). The soil pH gradient caused considerable changes in the concentrations of soil organic C and total N (Fig. 2). Organic C and the soil organic C/total N ratio all reached a maximum at around pH 5 and 6 and then levelled out until pH 8. In contrast, soil total N apparently peaked at pH 6,

Discussion

The close correlations between pH and biomass C, biomass ninhydrin-N, organic C and total N show that pH probably drives soil organic C input. The CO2 evolution was slightly more correlated with organic C than with pH suggesting that soil organic matter is an important factor associated with microbial biomass activity.

The biomass specific respiration quotient (qCO2) had the greatest values at high (above 7.5) and very low (below 4) pHs indicating a possible stress condition, i.e. more CO2–C was

Acknowledgements

We thank P. R. Poulton, Sarah Kemmitt and an anonymous referee for helpful advice and discussion. Rothamsted Research receives grant aided support from the Biotechnological and Biological Sciences Research Council. Juan Aciego also thanks the Council of Scientific and Humanistic Development (CDCH) of the Central University of Venezuela for financial support.

References (59)

  • M. Chagnon et al.

    Effects of experimental liming on collembolan communities and soil microbial biomass in a southern Quebec sugar maple (Acer saccharum Marsh.) stand

    Applied Soil Ecology

    (2001)
  • K. Chander et al.

    Microbial biomass dynamics during the decomposition of glucose and maize in metal-contaminated and non-contaminated soils

    Soil Biology & Biochemistry

    (1991)
  • K. Chander et al.

    Effects of heavy metals from past applications of sewage sludge on microbial biomass and organic matter accumulation in a sandy loam and silty loam U.K. soil

    Soil Biology & Biochemistry

    (1991)
  • K. Chander et al.

    Plant inputs of carbon to metal contaminated soil and effects on the soil microbial biomass

    Soil Biology & Biochemistry

    (1991)
  • K. Chander et al.

    Residual effects of zinc, copper and nickel in sewage sludge on microbial biomass in a sandy loam

    Soil Biology & Biochemistry

    (1993)
  • K. Chander et al.

    Synthesis of microbial biomass from added glucose in metal-contaminated and non-contaminated soils following repeated fumigation

    Soil Biology & Biochemistry

    (1992)
  • K. Chander et al.

    Microbial biomass dynamics following addition of metal-enriched sewage sludges to a sandy loam

    Soil Biology & Biochemistry

    (1995)
  • M.M. Couteaux et al.

    Anomalies in microbial biomass measurements in acid organic soils using extractable carbon following chloroform fumigation

    Soil Biology & Biochemistry

    (1990)
  • D. Curtin et al.

    Effects of acidity on mineralization: pH-dependence of organic matter mineralization in weakly acidic soils

    Soil Biology & Biochemistry

    (1998)
  • S.E. Flis et al.

    The interaction between aluminium and root nodule bacteria

    Soil Biology & Biochemistry

    (1993)
  • Å Frostegård et al.

    Shifts in the structure of soil microbial communities in limed forest as revealed by phospholipid fatty acid analysis

    Soil Biology & Biochemistry

    (1993)
  • K.E. Giller et al.

    Toxicity of heavy metals to microorganisms and microbial processes in agricultural soils: a review

    Soil Biology & Biochemistry

    (1998)
  • H. Insam

    Are the soil microbial biomass and basal respiration governed by the climatic regime?

    Soil Biology & Biochemistry

    (1990)
  • D.S. Jenkinson et al.

    The effects of biocidal treatments on metabolism in soil. V. A method for measuring soil biomass

    Soil Biology & Biochemistry

    (1976)
  • R.G. Joergensen et al.

    Ninhydrin-reactive nitrogen measurements of microbial biomass in 0.5 M K2SO4 soil extracts

    Soil Biology & Biochemistry

    (1990)
  • S.J. Kemmitt et al.

    Soil acidification used as a management strategy to reduce nitrate losses from agricultural land

    Soil Biology & Biochemistry

    (2005)
  • S.J. Kemmitt et al.

    pH regulation of carbon and nitrogen dynamics in two agricultural soils

    Soil Biology & Biochemistry

    (2006)
  • H. Marstorp et al.

    Relationship between dsDNA, chloroform labile C and ergosterol in soils of different organic matter contents and pH

    Soil Biology & Biochemistry

    (2000)
  • J.A. Ocio et al.

    An evaluation of methods for measuring the microbial biomass in soils following recent additions of wheat straw and the characterisation of the biomass that develops

    Soil Biology & Biochemistry

    (1990)
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