Volume 171, Issue 1 pp. 61-82
Review Article
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Organo-mineral associations in temperate soils: Integrating biology, mineralogy, and organic matter chemistry

Ingrid Kögel-Knabner

Ingrid Kögel-Knabner

Lehrstuhl für Bodenkunde, Department für Ökologie und Ökosystemmanagement, Wissenschaftszentrum Weihenstephan, Technische Universität München, 85350 Freising-Weihenstephan, Germany

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Georg Guggenberger

Georg Guggenberger

Institut für Agrar- und Ernährungswissenschaften, Martin-Luther-Universität Halle-Wittenberg, Weidenplan 14, 06108 Halle/Saale, Germany

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Markus Kleber

Markus Kleber

Department of Crop and Soil Science, Oregon State University, 3017 Ag & Life Sciences Bldg., Corvallis, OR 97331–7306, USA

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Ellen Kandeler

Ellen Kandeler

Institut für Bodenkunde und Standortslehre, Fachgebiet Bodenbiologie, Universität Hohenheim, Emil-Wolff-Straße 27, 70599 Stuttgart, Germany

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Karsten Kalbitz

Karsten Kalbitz

Lehrstuhl für Bodenökologie, Universität Bayreuth, 95440 Bayreuth, Germany

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Stefan Scheu

Stefan Scheu

Institut für Zoologie, Technische Universität Darmstadt, Schnittspahnstraße 3, 64287 Darmstadt, Germany

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Karin Eusterhues

Karin Eusterhues

Lehrstuhl für Bodenkunde, Department für Ökologie und Ökosystemmanagement, Wissenschaftszentrum Weihenstephan, Technische Universität München, 85350 Freising-Weihenstephan, Germany

present address: Chemisch-Geowissenschaftliche Fakultät, Friedrich-Schiller-Universität, Burgweg 11, 07749 Jena, Germany

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Peter Leinweber

Peter Leinweber

Institut für Landnutzung, Universität Rostock, Justus-von-Liebig-Weg 6, 18051 Rostock, Germany

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First published: 31 January 2008
Citations: 982

Topical Issue: Soils as a source and sink for CO2 – Mechanisms and regulation of organic matter stabilisation in soils (editors: I. Kögel-Knabner and E. Matzner). Synthesis of the DFG Priority Program SPP 1090 (German Research Foundation—“Deutsche Forschungsgemeinschaft”).

Abstract

We summarize progress with respect to (1) different approaches to isolate, extract, and quantify organo-mineral compounds from soils, (2) types of mineral surfaces and associated interactions, (3) the distribution and function of soil biota at organo-mineral surfaces, (4) the distribution and content of organo-mineral associations, and (5) the factors controlling the turnover of organic matter (OM) in organo-mineral associations from temperate soils. Physical fractionation achieves a rough separation between plant residues and mineral-associated OM, which makes density or particle-size fractionation a useful pretreatment for further differentiation of functional fractions. A part of the OM in organo-mineral associations resists different chemical treatments, but the data obtained cannot readily be compared among each other, and more research is necessary on the processes underlying resistance to treatments for certain OM components. Studies using physical-fractionation procedures followed by soil-microbiological analyses revealed that organo-mineral associations spatially isolate C sources from soil biota, making quantity and quality of OM in microhabitats an important factor controlling community composition. The distribution and activity of soil microorganisms at organo-mineral surfaces can additionally be modified by faunal activities. Composition of OM in organo-mineral associations is highly variable, with loamy soils having generally a higher contribution of polysaccharides, whereas mineral-associated OM in sandy soils is often more aliphatic. Though highly reactive towards Fe oxide surfaces, lignin and phenolic components are usually depleted in organo-mineral associations. Charred OM associated with the mineral surface contributes to a higher aromaticity in heavy fractions. The relative proportion of OC bound in organo-mineral fractions increases with soil depth. Likewise does the strength of the bonding. Organic molecules sorbed to the mineral surfaces or precipitated by Al are effectively stabilized, indicated by reduced susceptibility towards oxidative attack, higher thermal stability, and lower bioavailability. At higher surface loading, organic C is much better bioavailable, also indicated by little 14C age. In the subsurface horizons of the soils investigated in this study, Fe oxides seem to be the most important sorbents, whereas phyllosilicate surfaces may be comparatively more important in topsoils. Specific surface area of soil minerals is not always a good predictor for C-stabilization potentials because surface coverage is discontinuous. Recalcitrance and accessibility/aggregation seem to determine the turnover dynamics in fast and intermediate cycling OM pools, but for long-term OC preservation the interactions with mineral surfaces, and especially with Fe oxide surfaces, are a major control in all soils investigated here.

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