Exploring Surface Water-Bitumen Interactions in Athabasca Oil Sands Wetlands Using Stable and Radiocarbon Isotopes

IF 4.8 Q1 ENVIRONMENTAL SCIENCES
Ian J. Vander Meulen, Jason M. E. Ahad, Danna M. Schock, Lukas J. Mundy, Bruce D. Pauli, Dena W. McMartin and John V. Headley*, 
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引用次数: 0

Abstract

Naphthenic acid fraction compounds (NAFCs) have been identified as aquatic contaminants of concern associated with bitumen extraction in Canada’s Athabasca oil sands region. Previous investigations found that NAFCs occur and degrade in young (<100-year-old) wetlands, but the degree to which these NAFCs might be bitumen-derived remains unclear. To quantify contributions of modern versus fossil NAFCs, carbon isotope-based methods were applied to two intensively sampled wetlands suspected to be influenced by oil sands. Carbon-13 isotope ratios measured by pyrolytic decarboxylation (δ13Cpyr) fell within a narrow range (−27.5 to −26.0‰) and radiocarbon measurements (Δ14C) revealed a significant fossil carbon contribution (−795 to −290‰), presumably from bitumen. Along the flow pathway of one wetland, a positive shift of ∼1.5‰ in δ13Cpyr correlated with increasing distance from a suspected oil sands point source. Lower Δ14C values (i.e., less 14C) at this site corresponded to lighter δ13Cpyr r values – the opposite trend found in previous applications of δ13Cpyr analyses, whereby bitumen-derived NAFSs were around −22 to −21‰. This study shows how source attribution of NAFCs in surface water using δ13Cpyr may be less straightforward compared to groundwater, possibly due to differences in natural attenuation processes between these two environments.

Carbon isotope-based forensic techniques applied in the Athabasca oil sands region wetlands generated contrasting results, highlighting ambiguities in bitumen carbon mobility.

利用稳定碳同位素和放射性碳同位素探索阿萨巴斯卡油砂湿地地表水-沥青相互作用
环烷酸馏分化合物(NAFCs)已被确定为与加拿大阿萨巴斯卡油砂地区沥青开采相关的水生污染物。先前的研究发现,NAFCs在年轻(100年)的湿地中发生和降解,但这些NAFCs在多大程度上可能是沥青衍生的仍不清楚。为了量化现代NAFCs与化石NAFCs的贡献,研究人员将基于碳同位素的方法应用于两个疑似受油砂影响的密集采样湿地。热解脱羧测定的碳-13同位素比值(δ13Cpyr)下降在- 27.5 ~ - 26.0‰的窄范围内,放射性碳测量(Δ14C)显示化石碳贡献显著(- 795 ~ - 290‰),可能来自沥青。在一个湿地的流动路径上,δ13Cpyr的正位移为~ 1.5‰,与距离疑似油砂点源的距离增加有关。较低的Δ14C值(即较低的14C)对应于较轻的δ13Cpyr r值,这与以前δ13Cpyr分析应用中发现的趋势相反,即沥青衍生的nafs约为- 22至- 21‰。这项研究表明,与地下水相比,使用δ 13cypyr计算地表水中NAFCs的来源归属可能不太直接,这可能是由于这两种环境之间自然衰减过程的差异。在阿萨巴斯卡油砂区湿地应用的碳同位素法证技术产生了截然不同的结果,突出了沥青碳流动性的模糊性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
5.40
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