Wen Ke, Chadwick Oliver A, Vitousek Peter M, Paulus Elizabeth L, Landrot Gautier, Tappero Ryan V, Kaszuba John P, Luther George W, Wang Zimeng, Reinhart Benjamin J, Zhu Mengqiang
Department of Ecosystem Science and Management, University of Wyoming, Laramie, Wyoming82071, United States.
Department of Geography, University of California, Santa Barbara, California93106, United States.
Environ Sci Technol. 2023 Jan 10;57(1):730-740. doi: 10.1021/acs.est.2c02658. Epub 2022 Dec 20.
Manganese (Mn) exists as Mn(II), Mn(III), or Mn(IV) in soils, and the Mn oxidation state controls the roles of Mn in numerous environmental processes. However, the variations of Mn oxidation states with climate remain unknown. We determined the Mn oxidation states in highly weathered bulk volcanic soils (primary minerals free) across two rainfall gradients covering mean annual precipitation (MAP) of 0.25-5 m in the Hawaiian Islands. With increasing MAP, the soil redox conditions generally shifted from oxic to suboxic and to anoxic despite fluctuating at each site; concurrently, the proportions of Mn(IV) and Mn(II) decreased and increased, respectively. Mn(III) was low at both low and high MAP, but accumulated substantially, up to 80% of total Mn, in soils with prevalent suboxic conditions at intermediate MAP. Mn(III) was likely hosted in Mn(III,IV) and iron(III) oxides or complexed with organic matter, and its distribution among these hosts varied with soil redox potentials and soil pH. Soil redox conditions and rainfall-driven leaching jointly controlled exchangeable Mn(II) in soils, with its concentration peaking at intermediate MAP. The Mn redox chemistry was at disequilibrium, with the oxidation states correlating with long-term average soil redox potentials better than with soil pH. The soil redox conditions likely fluctuated between oxic and anoxic conditions more frequently at intermediate than at low and high MAP, creating biogeochemical hot spots where Mn, Fe, and other redox-sensitive elements may be actively cycled.
锰(Mn)在土壤中以二价锰(Mn(II))、三价锰(Mn(III))或四价锰(Mn(IV))的形式存在,锰的氧化态控制着锰在众多环境过程中的作用。然而,锰氧化态随气候的变化仍不为人知。我们测定了夏威夷群岛年平均降水量(MAP)为0.25 - 5米的两个降雨梯度上高度风化的块状火山土壤(无原生矿物)中的锰氧化态。随着MAP的增加,尽管每个地点存在波动,但土壤氧化还原条件总体上从有氧转变为缺氧和厌氧;同时,Mn(IV)和Mn(II)的比例分别下降和上升。Mn(III)在低MAP和高MAP时含量都较低,但在MAP中等且普遍存在缺氧条件的土壤中大量积累,高达总锰的80%。Mn(III)可能存在于Mn(III,IV)和铁(III)氧化物中或与有机物络合,其在这些宿主中的分布随土壤氧化还原电位和土壤pH值而变化。土壤氧化还原条件和降雨驱动的淋溶共同控制土壤中可交换的Mn(II),其浓度在MAP中等时达到峰值。锰的氧化还原化学处于不平衡状态,氧化态与长期平均土壤氧化还原电位的相关性优于与土壤pH值的相关性。在MAP中等时,土壤氧化还原条件可能比在低MAP和高MAP时更频繁地在有氧和厌氧条件之间波动,从而形成生物地球化学热点,锰、铁和其他对氧化还原敏感的元素可能在此处活跃循环。