Influence of pO2 on Iron Redox Cycling and Anaerobic Organic Carbon Mineralization in a Humid Tropical Forest Soil

被引:83
作者
Chen, Chunmei [1 ]
Meile, Christof [2 ]
Wilmoth, Jared [1 ]
Barcellos, Diego [1 ]
Thompson, Aaron [1 ]
机构
[1] Univ Georgia, Crop & Soil Sci, Athens, GA 30602 USA
[2] Univ Georgia, Marine Sci, Athens, GA 30602 USA
基金
美国国家科学基金会;
关键词
HYDROUS FERRIC-OXIDE; ATOM EXCHANGE; ISOTOPE FRACTIONATION; MICROBIAL COMMUNITIES; METHANE PRODUCTION; FERROUS IRON; PHOSPHORUS SOLUBILIZATION; HETEROGENEOUS OXIDATION; DISSIMILATORY REDUCTION; MATTER DECOMPOSITION;
D O I
10.1021/acs.est.8b01368
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ferrous iron (Fe-II) oxidation is an important pathway for generating reactive Fe-III phases in soils, which can affect organic carbon (OC) persistence/decomposition. We explored how pO(2) concentration influences Fe-II oxidation rates and Fe-III mineral composition, and how this impacts the subsequent Fe-III reduction and anaerobic OC mineralization following a transition from oxic to anoxic conditions. We conducted batch soil slurry experiments within a humid tropical forest soil amended with isotopically labeled Fe-57(II). The slurries were oxidized with either 21% or 1% PO2 for 9 days and then incubated for 20 days under anoxic conditions. Exposure to 21%pO(2) led to faster Fe-II oxidation rates and greater partitioning of the amended Fe-57 into low-crystallinity Fe-III-(oxyhydr)oxides (based on Mossbauer analysis) than exposure to 1% pO(2). During the subsequent anoxic period, low-crystallinity Fe-III-(oxyhydr)oxides were preferentially reduced relative to more crystalline forms with higher net rates of anoxic Fe-II and CO2 production-which were well correlated-following exposure to 21% pO(2) than to 1% pO(2) This study illustrates that in redox-dynamic systems, the magnitude of O-2 fluctuations can influence the coupled iron and organic carbon cycling in soils and more broadly, that reaction rates during periods of anoxia depend on the characteristics of prior oxidation events.
引用
收藏
页码:7709 / 7719
页数:11
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