Biochemically altered charcoal residues as an important source of soil organic matter in subsoils of fire-affected subtropical regions

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Although climatic conditions of subtropical regions support fast biochemical degradation of soil organic matter (SOM), some of their soils reveal dark umbric horizons with considerably high organic C contents. Since such soils can reach a depth of several meters a better understanding of the processes involved in the humification of its SOM is essential for an improved elucidation of the impact of the hot and humid conditions of subtropical regions on global C cycling. Therefore, the SOM of three Umbric Ferralsols from Brazil was characterized for its quantity and chemical composition as a function of soil depth. Solid-state 13C nuclear magnetic resonance (NMR) spectra revealed an increase of the aromaticity with soil depth to exceptionally high values between 40 and 70% of the SOM. Chemical oxidation of the SOM with acid potassium dichromate confirmed that a major part of this C group is attributable to pyrogenic organic matter (PyOM). High carboxyl-C contents between 13 and 21% of the total organic C in the subsoils showed that their PyOM is strongly oxidized, most likely due to previous intense biochemical reworking. Since the latter improves the water solubility of the formerly hydrophobic charcoal residues, such oxidized PyOM can be transported with the soil solution into deeper soil horizons. As indicated by the pattern of the 13C NMR spectra and the high C contents of the subsoil, the partially degraded PyOM seems to have lost its attractiveness to microbial attack with ongoing downward movement and accumulation. Correlating parameters of organic matter with those of soil mineralogy suggested that in addition to stabilization by the mineral phase other mechanisms must have contributed to the persistence of PyOM in the studied soils. Considering that in soils, microbial degradation of aromatic structures is mainly performed by lignolytic and aerobic organisms, we suggest that increasing oxygen depletion and unfavorable living conditions in the deeper soil regions decreased the activity of those organisms. This enhanced the biochemical recalcitrance of the aromatic PyOM whereas non-pyrogenic SOM was still subjected to degradation although most likely at a slower rate. As a consequence, the selective preservation of PyOM shifted not only the quality of the subsoil SOM toward higher aromaticity but also increased its quantity. Based on our results, we concluded that downward translocation of partially degraded PyOM and its subsequent accumulation represent important processes in soil systems which are frequently affected by fires. © 2015 Elsevier B.V.

The authors thank Pablo Vidal-Torrado, Márcia Calegari and Flávio Marques of the ESALQ of the Universidade de São Paulo (Brazil) for providing the soil samples. The Lehrstuhl für Bodenkunde of the Technische Universität München (Germany) and the Institute of Bioand Geosciences, Agrosphere (IBG-3) of the Forschungszentrum Jülich (Germany) are gratefully acknowledged for hosting the first author and giving her access to their NMR facilities. Comparably, the Centro de Investigación, Tecnología e Innovación of the Universidad de Sevilla (Spain) is thanked for allowing the use of their solid-state NMR instrument. The European Science Foundation (EG/3696) is acknowledged for the travel grant supplied from the activity entitled “Natural molecular structures as drivers and tracers of terrestrial C fluxes (MOLTER)” given to the first author.

Peer reviewed