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Iron oxidation stimulates organic matter decomposition in humid tropical forest soils.

机译:铁氧化刺激潮湿的热带森林土壤中的有机物分解。

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Humid tropical forests have the fastest rates of organic matter decomposition globally, which often coincide with fluctuating oxygen (O2) availability in surface soils. Microbial iron (Fe) reduction generates reduced iron [Fe(II)] under anaerobic conditions, which oxidizes to Fe(III) under subsequent aerobic conditions. We demonstrate that Fe (II) oxidation stimulates organic matter decomposition via two mechanisms: (i) organic matter oxidation, likely driven by reactive oxygen species; and (ii) increased dissolved organic carbon (DOC) availability, likely driven by acidification. Phenol oxidative activity increased linearly with Fe(II) concentrations (P<0.0001, pseudo R2=0.79) in soils sampled within and among five tropical forest sites. A similar pattern occurred in the absence of soil, suggesting an abiotic driver of this reaction. No phenol oxidative activity occurred in soils under anaerobic conditions, implying the importance of oxidants such as O2 or hydrogen peroxide (H2O2) in addition to Fe(II). Reactions between Fe(II) and H2O2 generate hydroxyl radical, a strong nonselective oxidant of organic compounds. We found increasing consumption of H2O2 as soil Fe(II) concentrations increased, suggesting that reactive oxygen species produced by Fe(II) oxidation explained variation in phenol oxidative activity among samples. Amending soils with Fe(II) at field concentrations stimulated short-term C mineralization by up to 270%, likely via a second mechanism. Oxidation of Fe(II) drove a decrease in pH and a monotonic increase in DOC; a decline of two pH units doubled DOC, likely stimulating microbial respiration. We obtained similar results by manipulating soil acidity independently of Fe(II), implying that Fe(II) oxidation affected C substrate availability via pH fluctuations, in addition to producing reactive oxygen species. Iron oxidation coupled to organic matter decomposition contributes to rapid rates of C cycling across humid tropical forests in spite of periodic O2 limitation, and may help explain the rapid turnover of complex C molecules in these soils.
机译:潮湿的热带森林在全球范围内分解有机物的速度最快,这通常与表层土壤中可利用的氧气(O 2 )波动有关。微生物中铁的还原在厌氧条件下会生成还原铁[Fe(II)],在随后的有氧条件下会氧化为Fe(III)。我们证明Fe(II)氧化通过两种机制刺激有机物分解:(i)有机物氧化,可能是由活性氧引起的; (ii)可能由于酸化作用而增加了溶解有机碳(DOC)的利用率。在五个热带森林地点内和之中采样的土壤中,苯酚的氧化活性随Fe(II)浓度线性增加(P <0.0001,假R 2 = 0.79)。在没有土壤的情况下也发生了类似的情况,表明该反应是非生物驱动因素。在厌氧条件下,土壤中没有苯酚的氧化活性,这表明氧化剂如O 2 或过氧化氢(H 2 O 2 )的重要性除了铁(II)。 Fe(II)与H 2 O 2 之间的反应生成羟基自由基,这是一种有机化合物的强非选择性氧化剂。我们发现随着土壤Fe(II)浓度的增加,H 2 O 2 的消耗量增加,这表明Fe(II)氧化产生的活性氧物种解释了酚氧化活性的变化在样本中。用田间浓度的Fe(II)修正土壤,可能通过第二种机制使短期C矿化最多增加270%。 Fe(II)的氧化导致pH值降低和DOC单调增加;两个pH单位的下降会使DOC翻倍,这可能会刺激微生物呼吸。通过独立于Fe(II)处理土壤酸度,我们得到了相似的结果,这表明Fe(II)氧化除了产生活性氧以外,还通过pH波动影响了C基质的利用率。尽管存在周期性的O 2 限制,但铁氧化与有机物分解结合仍有助于快速在潮湿的热带森林中循环碳,并有助于解释这些土壤中复杂C分子的快速周转。

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