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Redox controls on methane formation, migration and fate?in?shallow?aquifers

机译:氧化还原控制浅层含水层中甲烷的形成,迁移和命运

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Development of unconventional energy resources such as shale gas and coalbed methane has generated some public concern with regard to the protection of groundwater and surface water resources from leakage of stray gas from the deep subsurface. In terms of environmental impact to and risk assessment of shallow groundwater resources, the ultimate challenge is to distinguish (a)?natural in?situ production of biogenic methane, (b)?biogenic or thermogenic methane migration into shallow aquifers due to natural causes, and (c)?thermogenic methane migration from deep sources due to human activities associated with the exploitation of conventional or unconventional oil and gas resources. This study combines aqueous and gas (dissolved and free) geochemical and isotope data from 372 groundwater samples obtained from 186 monitoring wells of the provincial Groundwater Observation Well Network (GOWN) in Alberta (Canada), a province with a long record of conventional and unconventional hydrocarbon exploration. We investigated whether methane occurring in shallow groundwater formed in?situ, or whether it migrated into the shallow aquifers from elsewhere in the stratigraphic column. It was found that methane is ubiquitous in groundwater in Alberta and is predominantly of biogenic origin. The highest concentrations of biogenic methane (&??0.01?mM or ?&??0.2?mgmspace width="0.125em" linebreak="nobreak"/Lsup?1/sup), characterized by iδ/isup13/supCsubCHsub4/sub/sub values ?&???55?‰, occurred in anoxic Na-Cl, Na-HCOsub3/sub, and Na-HCOsub3/sub-Cl type groundwaters with negligible concentrations of nitrate and sulfate suggesting that methane was formed in?situ under methanogenic conditions for 39.1?% of the samples. In only a few cases (3.7?%) was methane of biogenic origin found in more oxidizing shallow aquifer portions suggesting limited upward migration from deeper methanogenic aquifers. Of the samples, 14.1?% contained methane with iδ/isup13/supCsubCHsub4/sub/sub values ?&???54?‰, potentially suggesting a thermogenic origin, but aqueous and isotope geochemistry data revealed that the elevated iδ/isup13/supCsubCHsub4/sub/sub values were caused by microbial oxidation of biogenic methane or post-sampling degradation of low CHsub4/sub content samples rather than migration of deep thermogenic gas. A significant number of samples (39.2?%) contained methane with predominantly biogenic C?isotope ratios (iδ/isup13/supCsubCHsub4/sub/sub?&???55?‰) accompanied by elevated concentrations of ethane and sometimes trace concentrations of propane. These gases, observed in 28.1?% of the samples, bearing both biogenic (iδ/isup13/supC) and thermogenic (presence of Csub3/sub) characteristics, are most likely derived from shallow coal seams that are prevalent in the Cretaceous Horseshoe Canyon and neighboring formations in which some of the groundwater wells are completed. The remaining 3.7?% of samples were not assigned because of conflicting parameters in the data sets or between replicates samples. Hence, despite quite variable gas concentrations and a wide range of iδ/isup13/supCsubCHsub4/sub/sub values in baseline groundwater samples, we found no conclusive evidence for deep thermogenic gas migration into shallow aquifers either naturally or via anthropogenically induced pathways in this baseline groundwater survey. This study shows that the combined interpretation of aqueous geochemistry data in concert with chemical and isotopic compositions of dissolved and/or free gas can
机译:页岩气和煤层气等非常规能源的开发引起了公众对于保护地下水和地表水资源免受深层地下杂散气体泄漏的关注。在对浅层地下水资源的环境影响和风险评估方面,最终的挑战是区分(a)生物甲烷的自然原位生产,(b)自然原因导致的生物或热甲烷迁移到浅层含水层, (c)由于与常规或非常规油气资源开采有关的人类活动,甲烷从深层热源迁移。这项研究结合了从阿尔伯塔省(加拿大)的省地下水观测井网(GOWN)的186口监测井获得的372个地下水样品中的水和气(溶解的和游离的)地球化学和同位素数据,该省拥有常规和非常规的悠久记录油气勘探。我们调查了在浅层地下水中产生的甲烷是否就地形成,还是从地层柱中的其他位置迁移到浅层含水层中。人们发现,阿尔伯塔省的地下水中甲烷无处不在,并且主要是生物成因。生物甲烷的最高浓度(&?0.01?mM或?&?0.2?mg L ?1 ),特征为δ 13 C CH 4 值? 3 和Na-HCO 3 -Cl型地下水,硝酸盐和硫酸盐的浓度可忽略不计,表明甲烷在甲烷化条件下原位形成。样品的39.1%。仅在少数情况下(3.7%)在较氧化的浅层含水层中发现了生物成因的甲烷,表明从较深的产甲烷含水层向上迁移有限。在这些样品中,有14.1%的甲烷具有δ 13 C CH 4 值? 54?‰,可能暗示其为热成因,但含水和同位素地球化学数据显示,升高的δ 13 C CH 4 < / sub>值是由生物甲烷的微生物氧化或低CH 4 含量的样品的采样后降解而不是深热气的迁移引起的。大量样品(39.2%)含有甲烷,且甲烷具有主要的生物碳同位素比(δ 13 C CH 4 < / sub>?<55≤‰)伴随着乙烷浓度的升高,有时还有痕量的丙烷。在28.1%的样品中观察到的这些气体具有生物成因(δ 13 C)和热成因(C 3 的存在)特征,很可能来自于白垩纪马蹄峡谷和其中一些地下水井完工的邻近地层中普遍存在的浅煤层。剩余的3.7%的样本未分配,因为数据集中或重复样本之间存在参数冲突。因此,尽管基线地下水样品中的气体浓度变化很大,并且δ 13 C CH 4 值范围很广,我们在此基线地下水调查中没有发现有结论性证据证明深热气会自然或通过人为诱发的途径向浅层含水层迁移。这项研究表明,结合溶解和/或游离气体的化学和同位素组成,可以对含水地球化学数据进行综合解释。

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