4.2 Article

Texture effects on carbon stabilisation and storage in New Zealand soils containing predominantly 2:1 clays

Journal

SOIL RESEARCH
Volume 54, Issue 1, Pages 30-37

Publisher

CSIRO PUBLISHING
DOI: 10.1071/SR14292

Keywords

C stabilisation by mineral particles; extractable Al & Fe; organic matter fractions

Categories

Funding

  1. New Zealand Agricultural Greenhouse Gas Research Centre
  2. Land Use Change and Intensification program of The New Zealand Institute for Plant & Food Research Limited

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Developing strategies to sequester carbon (C) in soils requires an understanding of the key factors that influence C stabilisation. Although fine mineral particles, especially clay, play a key role in stabilising soil organic matter (SOM), the relationship between SOM and texture is often not strong. We examined the role of the fine mineral fraction in C storage in sedimentary soils in New Zealand. Soils, representing two soil Orders (Brown and Recent) and different land use histories (total of 58 soils; 0-15cm depth) were sampled. The concentration of C (and N) in four particle size fractions (<5, 5-20, 20-50, >50 mu m) was determined (soils fractionated after dispersion by sonication). The soils had a wide range of textures and SOM; the mass proportion of clay (<5 mu m) ranged from 10 to 60g 100g(-1) and soil C from 16 to 45gkg(-1). Across both soil Orders and all land uses (dairy, sheep or beef, arable and vegetable cropping), the majority of soil C (57 to 66%) was stored in the clay fraction. However, there was no correlation (R-2=0.02; P>0.05) between the C concentration in whole soil and clay content. The concentration of C in the clay fraction, which varied over a wide range (35 to 135gkg(-1) clay), decreased as the mass proportion of clay increased. A similar trend in C concentration was observed for the fine (5-20 mu m) silt fraction. Because of this inverse relationship between the mass of the fine fractions and their C concentration, there was little change in amount of stable C (defined as C in the <20 mu m fraction) as the mass proportion of fine (<20 mu m) particles increased. Differences in pyrophosphate extractable aluminium explained part of the variability in C concentration in the fine fractions; however, we were unable to identify any specific physico-chemical factor that would account for the relatively low C concentrations observed in the <5 and 5-20 mu m fractions of fine-textured soils. We concluded that such soils may be under-saturated and potential may exist to store additional stable C.

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