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Photochemical behavior of dissolved and colloidal organic matter in estuarine and oceanic waters

机译:河口和海洋水中溶解和胶体有机物的光化学行为

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摘要

Chromophoric dissolved organic matter (CDOM), carbohydrates, and amino acids were analyzed to investigate the photochemistry of total dissolved (<0.22 µm) organic matter (DOM), high-molecular-weight (HMW, 1 kDa-0.22 µm) DOM and low-molecular-weight (LMW, <1 kDa) DOM at stations in the Yangtze River and its coastal area, and in the Western Pacific Ocean. Results revealed that the humic-like and tryptophan-like CDOM fluorescent components in riverine, coastal, and oceanic surface waters were photodegraded during irradiation. However, the photochemical behavior of tyrosine-like component was obscured by the excessive fluorescence intensities of humic- and tryptophan-like fluorescent components. Light sensitivity varied depending on the source material; terrestrially derived DOM was more susceptible to irradiation than autochthonous DOM. In contrast to the expected photodegradation of CDOM, photo-induced synthetic reaction transformed the LMW matters to polysaccharides (PCHO) and degradation reaction decomposed the HMW DOM to Monosaccharides. Colloidal DOM preferentially underwent photodegradation, whereas permeate DOM mainly photosynthesized PCHO. The total hydrolysable amino acid (THAA) pool changed because of the additional input by the photodegradation of DOM or THAA itself. The compositions of THAA changed during the irradiation experiments, indicating that the different photochemical behavior of individual amino acids were related to their different original photoreactivities; the relatively stable amino acids (e.g., Ser and Gly) significantly accumulated during irradiation, whereas photo-active aromatic amino acids (e.g. Tyr and His) were prone to photodegradation. The data presented here demonstrated that irradiation significantly influence the conversion between dissolved and colloid organic matter. These results can promote the understanding of irradiation effect on the carbon and nitrogen cycle in riverine, estuarine and oceanic ecosystems.
机译:分析了发色溶解有机物(CDOM),碳水化合物和氨基酸,以研究总溶解(<0.22 µm)有机物(DOM),高分子量(HMW,1 kDa-0.22 µm)和低DOM的光化学-分子量(LMW,<1 kDa)的DOM在长江及其沿海地区和西太平洋的站点。结果表明,在辐照过程中,河流,沿海和海洋地表水中的腐殖质样和色氨酸样CDOM荧光成分被光降解。然而,酪氨酸样组分的光化学行为被腐殖质和色氨酸样荧光组分的过量荧光强度所掩盖。光敏度因光源而异。陆地来源的DOM比自体DOM更容易受到辐射。与预期的CDOM光降解相反,光诱导的合成反应将LMW物质转化为多糖(PCHO),降解反应将HMW DOM分解为单糖。胶体DOM优先进行光降解,而渗透DOM主要是光合作用的PCHO。由于DOM或THAA本身的光降解而产生了额外的投入,因此总的可水解氨基酸(THAA)池发生了变化。 THAA的组成在辐照实验过程中发生了变化,表明单个氨基酸的不同光化学行为与其原始光反应性有关。相对稳定的氨基酸(例如Ser和Gly)在辐照过程中会大量积累,而光敏芳香族氨基酸(例如Tyr和His)则容易发生光降解。此处提供的数据表明,辐射显着影响溶解的有机物和胶体有机物之间的转化。这些结果可以促进人们了解辐照对河流,河口和海洋生态系统中碳和氮循环的影响。

著录项

  • 来源
    《The Science of the Total Environment》 |2017年第31期|214-224|共11页
  • 作者单位

    Key Laboratory of Marine Chemistry Theory and Technology, Ocean University of China, Ministry of Education/Qingdao Collaborative Innovation Center of Marine Science and Technology, Qingdao 266100, China,Institute of Marine Chemistry, Ocean University of China, Qingdao 266100, China;

    Key Laboratory of Marine Chemistry Theory and Technology, Ocean University of China, Ministry of Education/Qingdao Collaborative Innovation Center of Marine Science and Technology, Qingdao 266100, China,Laboratory for Marine Ecology and Environmental Science, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266200, China,Institute of Marine Chemistry, Ocean University of China, Qingdao 266100, China;

    Key Laboratory of Marine Chemistry Theory and Technology, Ocean University of China, Ministry of Education/Qingdao Collaborative Innovation Center of Marine Science and Technology, Qingdao 266100, China,Laboratory for Marine Ecology and Environmental Science, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266200, China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Chromophoric dissolved organic matter; (CDOM); Carbohydrates; Amino acids; Photochemistry; Colloidal organic matter;

    机译:发色溶解的有机物;(CDOM);碳水化合物;氨基酸;光化学;胶体有机质;

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