The role of Fe(III) in soil organic matter stabilization in two size fractions having opposite features
Creators
- 1. Department of Agricultural, Food and Environmental Sciences, Polytechnic University of Marche, via Brecce Bianche 10, 60131 Ancona (Italy)
- 2. Department of the Sciences of Agriculture, Food and Environment, University of Foggia, via Napoli 25, 71122 Foggia (Italy)
- 3. Instituto de Ciencias Agrarias, Consejo Superior de Investigaciones Científicas, Serrano 115 bis, 28006 Madrid (Spain)
- 4. Delaware Environmental Institute, University of Delaware, Interdisciplinary Science and Engineering (ISE) Laboratory, 221 Academy Street, Newark, DE 19716 (United States)
- 5. Forest Sciences and Technology Center of Catalonia, Carretera St Llorenç de Morunys, km 2, 25280 Solsona (Spain)
- 6. Department of Plant and Soil Sciences, University of Delaware, Interdisciplinary Science and Engineering (ISE) Laboratory, 221 Academy Street, Newark, DE 19716 (United States)
Description
Highlights: • Fe(III) controls organic C stabilization in fine silt and clay and fine sand SOM fractions. • Fe(III) addition caused a decrease in the organic C in the solution. • The stabilization effect was larger for the fine sand SOM fraction. • The reaction with Fe(III) may promote either flocculation or coating phenomena. • The organic C retained after Fe-mediated stabilization has low sensitivity to desorption. -- Abstract: Soil organic matter (SOM) protection, stability and long-term accumulation are controlled by several factors, including sorption onto mineral surfaces. Iron (Fe) has been suggested as a key regulator of SOM stability, both in acidic conditions, where Fe(III) is soluble, and in near-neutral pH environments, where it precipitates as Fe(III) (hydr)oxides. The present study aimed to probe, by sorption/desorption experiments in which Fe was added to the system, the mechanisms controlling Fe(III)-mediated organic carbon (C) stabilization; fine silt and clay (FSi + Cl) and fine sand (FSa) SOM fractions of three soils under different land uses were tested. Fe(III) addition caused a decrease in the organic C remaining in solution after reaction, indicating an Fe-mediated organic C stabilization effect. This effect was two times larger for FSa than for FSi + Cl, the former fraction being characterized by both low specific surface area and high organic C content. The organic C retained in the solid phase after Fe-mediated stabilization has relatively low sensitivity to desorption. Moreover, attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy indicated that Fe-mediated organic C stabilization can be mainly ascribed to the formation of complexes between carbohydrate OH functional groups and Fe oxides. These results demonstrate that the binding of labile SOM compounds to Fe(III) contributes to its preservation, and that the mechanisms involved (flocculation vs. coating) depend on the size fractions.
Additional details
Additional titles
- Augmented title (English)
- Sorption/desorption experiments;Physical fractionation;C cycle;Coprecipitation;Ferrihydrite
Identifiers
- DOI
- 10.1016/j.scitotenv.2018.10.361;
- PII
- S004896971834261X;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 653
- Journal Page Range
- p. 667-674
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55103937
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- DESORPTION; FLOCCULATION; FOURIER TRANSFORM SPECTROMETERS; FRACTIONATION; INFRARED SPECTRA; IRON; IRON OXIDES; ORGANIC MATTER; OXIDES; SAND; SENSITIVITY; SILT; SOILS; SORPTION; STABILIZATION; SURFACES
- Descriptors DEC
- CHALCOGENIDES; ELEMENTS; IRON COMPOUNDS; MATTER; MEASURING INSTRUMENTS; METALS; OXIDES; OXYGEN COMPOUNDS; PRECIPITATION; SEPARATION PROCESSES; SORPTION; SPECTRA; SPECTROMETERS; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier B.V. All rights reserved.