铁酸盐
矿化(土壤科学)
化学
葡萄糖醛酸
环境化学
共沉淀
缺氧水域
溶解有机碳
腐植酸
有机质
溶解
土壤水分
土壤有机质
地质学
无机化学
土壤科学
有机化学
吸附
多糖
肥料
作者
Laurel K. ThomasArrigo,Sophie Vontobel,Luiza Notini,Tabea Nydegger
标识
DOI:10.1021/acs.est.3c01336
摘要
It is known that the association of soil organic matter (SOM) with iron minerals limits carbon mobilization and degradation in aerobic soils and sediments. However, the efficacy of iron mineral protection mechanisms under reducing soil conditions, where Fe(III)-bearing minerals may be used as terminal electron acceptors, is poorly understood. Here, we quantified the extent to which iron mineral protection inhibits mineralization of organic carbon in reduced soils by adding dissolved 13C-glucuronic acid, a 57Fe-ferrihydrite-13C-glucuronic acid coprecipitate, or pure 57Fe-ferrihydrite to anoxic soil slurries. In tracking the re-partitioning and transformation of 13C-glucuronic acid and native SOM, we find that coprecipitation suppresses mineralization of 13C-glucuronic acid by 56% after 2 weeks (at 25 °C) and decreases to 27% after 6 weeks, owing to ongoing reductive dissolution of the coprecipitated 57Fe-ferrihydrite. Addition of both dissolved and coprecipitated 13C-glucuronic acid resulted in increased native SOM mineralization, but the reduced bioavailability of the coprecipitated versus dissolved 13C-glucuronic acid decreased the priming effect by 35%. In contrast, the addition of pure 57Fe-ferrihydrite resulted in negligible changes in native SOM mineralization. Our results show that iron mineral protection mechanisms are relevant for understanding the mobilization and degradation of SOM under reducing soil conditions.
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