Stability of elemental carbon in a savanna soil

Citation
Mi. Bird et al., Stability of elemental carbon in a savanna soil, GLOBAL BIOG, 13(4), 1999, pp. 923-932
Citations number
30
Categorie Soggetti
Earth Sciences
Journal title
GLOBAL BIOGEOCHEMICAL CYCLES
ISSN journal
08866236 → ACNP
Volume
13
Issue
4
Year of publication
1999
Pages
923 - 932
Database
ISI
SICI code
0886-6236(199912)13:4<923:SOECIA>2.0.ZU;2-G
Abstract
(W)e have investigated the stability of oxidation-resistant elemental carbo n (OREC) in a sandy savanna soil at the Matopos fire trial site, Zimbabwe. The protection of some soil plots from fire for the last 50 years at this s ite has enabled a comparison of OREC abundances between those plots which h ave been protected from fire and plots which have continued to be burnt. Th e total 0-5 cm OREC inventory of the soil protected from fire is estimated to be 2.0+/-0.5 mg cm(-2); approximately half the "natural" OREC inventory at the study site of 3.8+/-0.5 mg cm(-2) (the mean for plots burnt every 1- 5 years). The associated half-life for natural OREC loss from the 0-5 cm in terval of the protected plots is calculated to be <100 years, with the half -life for large carbonized particles (>2000 mu m) in the soil being conside rably <50 years. These results suggest that at least in well-aerated tropic al soil environments, charcoal and OREC can be can be significantly degrade d on decadal to centennial timescales. OREC abundance and carbon-isotope da ta suggest that OREC in coarse particles is progressively degraded into fin er particle sizes, with a concomitant increase in resistance to oxidative d egradation of OREC in the finer particle sizes due to the progressive loss of more readily degraded OREC. It remains unclear whether the OREC that is degraded is oxidized completely to CO2 and subsequently emitted from the so il, reduced to a sufficiently small particle size to be illuviated to deepe r parts of the soil profile, solubilized and lost from the profile as disso lved organic carbon or transmuted into a chemical form which is susceptible to attack by the acid-dichromate reagent. The conclusion that a significan t proportion of OREC can undergo natural degradation in well-aerated enviro nments on decadal/centennial timescales suggests that only a fraction of th e total production of OREC from biomass burning and fossil fuel combustion is likely to be sequestered in the slow-cycling "geological" carbon reservo ir.