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Impact of Photooxidation and Biodegradation on the Fate of Oil Spilled During the Deepwater Horizon Incident: Advanced Stages of Weathering

机译:光氧化和生物降解对深水地平线事件中溢油命运的影响:风化的晚期

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摘要

While the biogeochemical forces influencing the weathering of spilled oil have been investigated for decades, the environmental fate and effects of "oxyhydrocarbons" in sand patties deposited on beaches are not well-known. We collected sand patties deposited in the swash zone on Gulf of Mexico beaches following the Deepwater Horizon oil spill. When sand patties were exposed to simulated sunlight, a larger concentration of dissolved organic carbon was leached into seawater than the corresponding dark controls. This result was consistent with the general ease of movement of seawater through the sand patties as shown with a ~(35)SO_4~(2-) radiotracer. Ultrahigh-resolution mass spectrometry, as well as optical measurements revealed that the chemical composition of dissolved organic matter (DOM) leached from the sand patties under dark and irradiated conditions were substantially different, but neither had a significant inhibitory influence on the endogenous rate of aerobic or anaerobic microbial respiratory activity. Rather, the dissolved organic photooxidation products stimulated significantly more microbial O_2 consumption (113 ± 4 μM) than either the dark (78 ± 2 μM) controls or the endogenous (38 μM ± 4) forms of DOM. The changes in the DOM quality and quantity were consistent with biodegradation as an explanation for the differences. These results confirm that sand patties undergo a gradual dissolution of DOM in both the dark and in the light, but photooxidation accelerates the production of water-soluble polar organic compounds that are relatively more amenable to aerobic biodegradation. As such, these processes represent previously unrecognized advanced weathering stages that are important in the ultimate transformation of spilled crude oil.
机译:尽管数十年来已经研究了影响溢油老化的生物地球化学作用力,但环境命运和“含氧碳氢化合物”对沉积在海滩上的沙饼的影响尚不为人所知。在“深水地平线”漏油事件发生后,我们收集了沉积在墨西哥湾海滩斜流带上的沙饼。当沙饼暴露在模拟的阳光下时,与相应的深色对照相比,更大浓度的溶解有机碳被淋入海水。该结果与海水通过砂饼移动的总体容易程度一致,如〜(35)SO_4〜(2-)放射性示踪剂所示。超高分辨率质谱法和光学测量表明,在黑暗和辐射条件下从沙饼中沥出的溶解有机物(DOM)的化学成分有很大不同,但都没有对内生需氧率产生显着抑制作用或厌氧微生物的呼吸活动。相反,溶解的有机光氧化产物比暗对照(78±2μM)或内源(38μM±4)形式的DOM刺激的微生物O_2消耗量大得多(113±4μM)。 DOM质和量的变化与生物降解相一致,以解释差异。这些结果证实,沙饼在黑暗和光线下都逐渐溶解DOM,但是光氧化作用加速了水溶性极性有机化合物的产生,而水溶性极性有机化合物相对而言更适合于需氧生物降解。因此,这些过程代表了以前无法识别的高级风化阶段,这对溢油的最终转化至关重要。

著录项

  • 来源
    《Environmental Science & Technology》 |2017年第13期|7412-7421|共10页
  • 作者单位

    Department of Microbiology and Plant Biology, University of Oklahoma, Norman, Oklahoma 73019,Institute for Energy and the Environment, University of Oklahoma, Norman, Oklahoma 73019;

    National High Magnetic Field Laboratory, Florida State University, Tallahassee, Florida 32310-3706;

    National High Magnetic Field Laboratory, Florida State University, Tallahassee, Florida 32310-3706,Department of Earth, Ocean and Atmospheric Science, Florida State University, Tallahassee, Florida 32306;

    Department of Chemistry, University of New Orleans, New Orleans, Louisiana 70148;

    Department of Microbiology and Plant Biology, University of Oklahoma, Norman, Oklahoma 73019,Institute for Energy and the Environment, University of Oklahoma, Norman, Oklahoma 73019;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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