Nicot Jean-Philippe, Larson Toti, Darvari Roxana, Mickler Patrick, Uhlman Kristine, Costley Ruth
Bureau of Economic Geology, Jackson School of Geosciences, The University of Texas at Austin, 10100 Burnet Road, Austin, TX.
Department of Geological Sciences, Jackson School of Geosciences, The University of Texas at Austin, 2305 Speedway, Austin, TX.
Ground Water. 2017 Jul;55(4):455-468. doi: 10.1111/gwat.12506. Epub 2017 Mar 2.
Assessing natural vs. anthropogenic sources of methane in drinking water aquifers is a critical issue in areas of shale oil and gas production. The objective of this study was to determine controls on methane occurrences in aquifers in the Eagle Ford Shale play footprint. A total of 110 water wells were tested for dissolved light alkanes, isotopes of methane, and major ions, mostly in the eastern section of the play. Multiple aquifers were sampled with approximately 47 samples from the Carrizo-Wilcox Aquifer (250-1200 m depth range) and Queen City-Sparta Aquifer (150-900 m depth range) and 63 samples from other shallow aquifers but mostly from the Catahoula Formation (depth <150 m). Besides three shallow wells with unambiguously microbial methane, only deeper wells show significant dissolved methane (22 samples >1 mg/L, 10 samples >10 mg/L). No dissolved methane samples exhibit thermogenic characteristics that would link them unequivocally to oil and gas sourced from the Eagle Ford Shale. In particular, the well water samples contain very little or no ethane and propane (C1/C2+C3 molar ratio >453), unlike what would be expected in an oil province, but they also display relatively heavier δ C (>-55‰) and δD (>-180‰). Samples from the deeper Carrizo and Queen City aquifers are consistent with microbial methane sourced from syndepositional organic matter mixed with thermogenic methane input, most likely originating from deeper oil reservoirs and migrating through fault zones. Active oxidation of methane pushes δ C and δD toward heavier values, whereas the thermogenic gas component is enriched with methane owing to a long migration path resulting in a higher C1/C2+C3 ratio than in the local reservoirs.
评估饮用水含水层中甲烷的自然源与人为源是页岩油和天然气生产地区的一个关键问题。本研究的目的是确定对伊格福特页岩区含水层中甲烷出现情况的控制因素。总共对110口水井进行了溶解态轻烷烃、甲烷同位素和主要离子的测试,大部分测试在该区域的东部进行。对多个含水层进行了采样,从卡里佐 - 威尔科克斯含水层(深度范围为250 - 1200米)和皇后城 - 斯巴达含水层(深度范围为150 - 900米)采集了约47个样本,从其他浅层含水层(但大多来自卡塔胡拉组,深度<150米)采集了63个样本。除了三口明确含有微生物成因甲烷的浅井外,只有较深的井显示出显著的溶解态甲烷(22个样本>1毫克/升,10个样本>10毫克/升)。没有溶解态甲烷样本表现出能将它们明确与伊格福特页岩来源的油气联系起来的热成因特征。特别是,井水样本中乙烷和丙烷含量极少或没有(C1/C2 + C3摩尔比>453),这与油区的预期情况不同,但它们的δC(>-55‰)和δD(>-180‰)也相对较重。来自较深的卡里佐和皇后城含水层的样本与源自同沉积有机质并混合了热成因甲烷输入的微生物成因甲烷一致,热成因甲烷很可能源自更深的油藏并通过断层带运移。甲烷的活跃氧化使δC和δD值向较重方向变化,而热成因气体成分由于长距离运移路径导致C1/C2 + C3比值高于当地油藏,从而富含甲烷。