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Phosphate oxygen isotope evidence for methylphosphonate sources of methane and dissolved inorganic phosphate

机译:甲烷和溶解的无机磷酸盐的甲基磷酸盐来源的磷酸盐氧同位素证据

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The ocean is an important source of methane, however, the sources of oceanic methane and mechanisms of its release to the atmosphere have only recently begun to be understood. Recent studies have identified methylphosphonate (MPn) as a previously unknown and likely source of methane in the aerobic ocean (Karl et al., 2008), as well as shown the biosynthesis of methylphosphonic acid to be a widespread trait in marine microbes (Metcalf et al., 2012). The mechanisms and reaction pathways from MPn to free methane, however, have not been well studied. Here we present results of laboratory studies on the photo-degradation of MPn, a likely mechanism of methane release to the atmosphere and phosphate release to the surface oceans. Phosphonoacetic acid was also studied as an additional model compound for comparison. We used the multi-labeled water isotope probing (MLWIP) approach, involving O-18-labeled waters to probe the photolytic mechanism of C-P bond cleavage in phosphates through analysis of P released from MPn as PO4. These studies identified distinct reaction pathways involving phosphates compared with other common organophosphorus compounds (e.g., phosphoesters), as well as suggest the involvement of both ambient water and atmospheric oxygen in C-P bond cleavage. There is only a small amount of water oxygen incorporated into product PO4 after cleavage of the C-P bond in MPn, suggesting atmospheric O-2 or radicals formed from O-2 under Ultra Violet Radiation (UVR), as the primary source of O that replaces C in the C-P bond of MPn. Model calculations suggest that the delta O-18(P) signature of phosphate released via UV-degradation of phosphates is largely (75%) inherited from the original phosphate substrate. This opens up the possibility of tracing and differentiating specific phosphate sources of dissolved phosphate from other organophosphorus (Porg) sources (e.g., phosphoesters) used in primary production, as well as for tracing specific MPn sources of atmospheric methane. (C) 2018 Published by Elsevier B.V.
机译:海洋是甲烷的重要来源,但是,直到最近才开始了解海洋甲烷的来源及其向大气释放的机制。最近的研究已将甲基膦酸酯(MPn)鉴定为好氧海洋中甲烷的先前未知且可能的来源(Karl等,2008),并表明甲基膦酸的生物合成是海洋微生物中的普遍特征(Metcalf et al。等人,2012年)。从MPn到游离甲烷的机理和反应途径尚未得到很好的研究。在这里,我们介绍了MPn光降解的实验室研究结果,MPn是甲烷释放到大气中和磷酸盐释放到海洋中的一种可能机制。还研究了膦乙酸作为另一种用于比较的模型化合物。我们使用多标记水同位素探测(MLWIP)方法,涉及O-18标记的水,通过分析从MPn中以PO4形式释放的P来研究磷酸盐中C-P键裂解的光解机理。这些研究确定了与其他常见的有机磷化合物(例如磷酸酯)相比涉及磷酸盐的独特反应途径,并且表明环境水和大气氧都参与了C-P键的裂解。在MPn中的CP键断裂后,只有少量的水氧结合到产物PO4中,这表明在紫外线辐射(UVR)下,大气中的O-2或由O-2形成的自由基是取代O的主要来源MPn的CP键中的C。模型计算表明,通过磷酸盐的UV降解释放的磷酸盐的δO-18(P)签名很大程度上(75%)来自原始磷酸盐底物。这开辟了将溶解的磷酸盐的特定磷酸盐源与主要生产中使用的其他有机磷(Porg)源(例如磷酸酯)进行追踪和区分的可能性,以及用于追踪大气甲烷的特定MPn来源的可能性。 (C)2018由Elsevier B.V.发布

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