Department of Marine Chemistry & Geochemistry, Woods Hole Oceanographic Institution , Woods Hole, Massachusetts 02543, United States.
Environ Sci Technol. 2014 Jun 17;48(12):6726-34. doi: 10.1021/es500825q. Epub 2014 Jun 2.
Petroleum biomarkers such as hopanoids, steranes, and triaromatic steroids (TAS) are commonly used to investigate the source and fate of petroleum hydrocarbons in the environment based on the premise that these compounds are resistant to biotic and abiotic degradation. To test the validity of this premise in the context of the Deepwater Horizon disaster, we investigated changes to these biomarkers as induced by natural weathering of crude oil discharged from the Macondo Well (MW). For surface slicks collected from May to June in 2010, and other oiled samples collected on beaches in the northern Gulf of Mexico from July 2010 until August 2012, hopanoids with up to 31 carbons as well as steranes and diasteranes were not systematically affected by weathering processes. In contrast, TAS and C32- to C35-homohopanes were depleted in all samples relative to 17α(H),21β(H)-hopane (C30-hopane). Compared to MW oil, C35-homohopanes and TAS were depleted by 18 ± 10% and 36 ± 20%, respectively, in surface slicks collected from May to June 2010, and by 37 ± 9% and 67 ± 10%, respectively, in samples collected along beaches from April 2011 through August 2012. Based on patterns of relative losses of individual compounds, we hypothesize biodegradation and photooxidation as main degradation processes for homohopanes and TAS, respectively. This study highlights that (i) TAS and homohopanes can be degraded within several years following an oil spill, (ii) the use of homohopanes and TAS for oil spill forensics must account for degradation, and (iii) these compounds provide a window to parse biodegradation and photooxidation during advanced stages of oil weathering.
石油生物标志物,如藿烷类、甾烷类和三芳甾族化合物(TAS),通常用于根据这些化合物不易受生物和非生物降解的前提,研究环境中石油烃的来源和归宿。为了检验这一前提在深海地平线灾难背景下的有效性,我们调查了由于从马孔多井(MW)排放的原油的自然风化而引起的这些生物标志物的变化。对于 2010 年 5 月至 6 月采集的表层浮油以及 2010 年 7 月至 2012 年 8 月在墨西哥湾北部海滩采集的其他油污样本,多达 31 个碳原子的藿烷类、甾烷类和 diasteranes 并没有受到风化过程的系统影响。相比之下,在所有样本中,TAS 和 C32 至 C35-同藿烷都相对于 17α(H),21β(H)-藿烷(C30-藿烷)被耗尽。与 MW 油相比,在 2010 年 5 月至 6 月采集的表层浮油中,C35-同藿烷和 TAS 分别减少了 18±10%和 36±20%,而在 2011 年 4 月至 2012 年 8 月期间在海滩上采集的样本中,分别减少了 37±9%和 67±10%。基于个别化合物相对损失的模式,我们假设生物降解和光氧化分别是同藿烷和 TAS 的主要降解过程。这项研究强调了:(i)在石油泄漏后的几年内,TAS 和同藿烷可能会被降解;(ii)在石油泄漏取证中使用同藿烷和 TAS 必须考虑降解;(iii)这些化合物提供了一个窗口,可以在石油风化的后期阶段解析生物降解和光氧化。