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东热带北大西洋中超氧化物(O2(-))的衰减途径。

Pathways of superoxide (O2(-)) decay in the Eastern Tropical North Atlantic.

机构信息

Marine Biogeochemistry, GEOMAR Helmholtz Centre for Ocean Research Kiel, Düsternbrooker Weg 20, 24105 Kiel, Germany.

出版信息

Environ Sci Technol. 2013 Sep 17;47(18):10249-56. doi: 10.1021/es401658t. Epub 2013 Aug 26.

Abstract

Superoxide (O2(-): IUPAC name dioxide (•1-)) is an important transient reactive oxygen species (ROS) in the ocean formed as an intermediate in the redox transformation of oxygen (O2) into hydrogen peroxide (H2O2) and vice versa. This highly reactive and very short-lived radical anion can be produced both via photochemical and biological processes in the ocean. In this paper we examine the decomposition rate of O2(-) throughout the water column, using new data collected in the Eastern Tropical North Atlantic (ETNA) Ocean. For this approach we applied a semi factorial experimental design to identify and quantify the pathways of the major identified sinks in the ocean. In this work we occupied six stations, two on the West African continental shelf and four open ocean stations, including the CVOO time series site adjacent to Cape Verde. Our results indicate that, in the surface ocean impacted by Saharan aerosols and coastal sediment resuspension, the main decay pathways for superoxide are via reactions with Mn(II) and organic matter.

摘要

超氧阴离子自由基(O2(-):IUPAC 名称为二氧化物(•1-))是海洋中一种重要的瞬态活性氧物质(ROS),它是氧气(O2)向过氧化氢(H2O2)和反之转化过程中的氧化还原转化的中间产物。这种高反应性和极短寿命的自由基阴离子可以通过海洋中的光化学和生物过程产生。在本文中,我们使用在东热带北大西洋(ETNA)海洋中收集的新数据,研究了整个水柱中 O2(-)的分解速率。为此,我们采用了半析因实验设计来识别和量化海洋中主要确定的汇的途径。在这项工作中,我们占据了六个站点,两个在西非大陆架上,四个在开阔海域,包括毗邻佛得角的 CVOO 时间序列站点。我们的结果表明,在受撒哈拉气溶胶和沿海沉积物再悬浮影响的海洋表面,超氧阴离子自由基的主要衰减途径是与 Mn(II)和有机物反应。

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