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In the last two decades, permanganate has been used to define what is assumed to be a labile or “active” soil carbon (C) pool, commonly referred to as “permanganate‐oxidizable carbon” (POXC). However, uncertainties in the reduction reaction (Mn 7+ → Mn 4+ /Mn 2+ ) and even greater uncertainties in the oxidation reaction (C ? → C ? ) as well as the reaction of non‐C reductants in the soil sample preclude the calculation of milligram C per kilogram of soil oxidized. Combined variation in the reduction–oxidation reactions can entail up to fivefold variation in how much soil organic C is oxidized per unit permanganate reduced. Without determining final reduction state of Mn and the initial and final oxidation states of C, the amount of C oxidized cannot be calculated. Unless a concrete understanding of the reduction and oxidation half‐reactions is achieved, an alternative expression of permanganate reactivity of a soil sample (i.e., not mg C kg −1 soil) is needed.
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Margenot et al. (2024) studied this question.
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