溶解有机碳
地下水
环境科学
碳循环
海底地下水排放
环境化学
碳纤维
地表水
有机质
总有机碳
降级(电信)
水文学(农业)
化学
环境工程
地质学
含水层
生态学
生态系统
材料科学
生物
复合数
电信
复合材料
有机化学
岩土工程
计算机科学
作者
Liza McDonough,Martin S. Andersen,M. I. Behnke,Helen Rutlidge,Phetdala Oudone,Karina Meredith,D. M. O'Carroll,Isaac R. Santos,Christopher E. Marjo,Robert G. M. Spencer,Amy M. McKenna,Andy Baker
标识
DOI:10.1038/s41467-022-29711-9
摘要
Groundwater comprises 95% of the liquid fresh water on Earth and contains a diverse mix of dissolved organic matter (DOM) molecules which play a significant role in the global carbon cycle. Currently, the storage times and degradation pathways of groundwater DOM are unclear, preventing an accurate estimate of groundwater carbon sources and sinks for global carbon budgets. Here we reveal the transformations of DOM in aging groundwater using ultra-high resolution mass spectrometry combined with radiocarbon dating. Long-term anoxia and a lack of photodegradation leads to the removal of oxidised DOM and a build-up of both reduced photodegradable formulae and aerobically biolabile formulae with a strong microbial signal. This contrasts with the degradation pathway of DOM in oxic marine, river, and lake systems. Our findings suggest that processes such as groundwater extraction and subterranean groundwater discharge to oceans could result in up to 13 Tg of highly photolabile and aerobically biolabile groundwater dissolved organic carbon released to surface environments per year, where it can be rapidly degraded. These findings highlight the importance of considering groundwater DOM in global carbon budgets.
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