Abstract

The onset of oxic-anoxic events in soil induces biogeochemical processes that may have profound influences on the fate and transport of soil organic carbon (OC). An 18-wk long laboratory soil column study was conducted to investigate the influence of static oxic (SO), static anoxic (SA), or redox oscillation (RO) events on the release of OC. Column leachate samples were collected after 9-wk and 18-wk of incubations and separated into dissolved (<2.3 nm), natural nanoparticle (2.3–100 nm), fine colloid (100–450 nm), and particulate (> 450 nm) fractions that were characterized through spectrofluorometric analyses. The concentration of released OC from different treatment columns followed the order of SA > RO > SO. After 9-wk, total OC concentrations in the leachate samples were increased by 4-fold and 54-fold in the SO and SA columns compared to the time-zero control columns, respectively. However, after 18-wk, the released amount of OC doubled in SO but decreased by 50 % in SA columns compared to the 9-wk incubation samples. The RO columns had intermediate OC concentrations between the SO and SA treatments. The RO events further led to widely varied dynamics in the release and molecular composition of the size-fractionated OC compared to static conditions, indicating the effects of redox oscillation on the organo-mineral association in soil. The wide variations in the aromaticity of OC released after the 1st and 2nd RO events further support the notion that alternating redox processes regulate OC cycling differently than the SO or SA condition. The observed increase in fine colloid and particulate OC fractions (i.e., >100 nm) from 7 % to 40 % between 1st and 2nd RO suggests the clustering of nanoaggregates and/or formation of colloidal size aggregates. The composition of the released OC as influenced by redox fluctuations provides a baseline for the size continuum of soil OC and its potential ecological and environmental roles.

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