Priority Organization for Innovation and Excellence, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555, Japan.
Sci Total Environ. 2011 Jun 1;409(13):2541-54. doi: 10.1016/j.scitotenv.2011.03.039. Epub 2011 Apr 19.
The sources of sulfate in an aquifer system, and its formation/degradation via biogeochemical reactions, were investigated by determining sulfate isotope ratios (δ³⁴S(SO₄) and δ¹⁸O(SO₄) in dissolved sulfate in groundwater from the Jakarta Basin. The groundwater flow paths, water ages, and geochemical features are well known from previous studies, providing a framework for the groundwater chemical and isotopic data, which is supplemented with data for spring water, river water, hot spring water, seawater, detergents, and fertilizers within the basin. The sulfate isotope composition of groundwater samples varied widely from -2.9‰ to +33.4‰ for δ³⁴S(SO₄) and +4.9‰ to +17.8‰ for δ¹⁸O(SO₄) and changed systematically along its flow direction from the mountains north to the coastal area. The groundwater samples were classified into three groups showing (1) relatively low and narrow δ(34)S(SO₄) (+2.3‰ to +7.6‰) with low and varied δ¹⁸O(SO₄) (+4.9‰ to +12.9‰) compositions, (2) high and varied δ³⁴S(SO₄) (+10.2‰ to +33.4‰) with high δ¹⁸O(SO₄) (+12.4‰ to +17.3‰) compositions, and (3) low δ³⁴S(SO₄) (< +6.1‰) with high δ¹⁸O(SO₄) (up to +17.8‰) compositions. These three types of groundwater were observed in the terrestrial unconfined aquifer, the coastal unconfined and confined aquifers, and the terrestrial confined aquifer, respectively. A combination of field measurements, concentrations, and previously determined δ¹⁵N(NO₃) data, showed that the observed isotopic heterogeneity was mainly the result of contributions of pollutants from domestic sewage in the rural area, mixing of seawater sulfate that had experienced previous bacterial sulfate reduction in the coastal area, and isotopic fractionation during the formation of sulfate through bacterial disproportionation of elemental sulfur. Our results clearly support the hypothesis that human impacts are important factors in understanding the sulfur cycle in present-day subsurface environments. A general model of sulfate isotopic evolution along with groundwater flow has rarely been proposed, due to the complicated hydrogeological research setting that causes varied isotope ratios, although its understanding has recently received great attention. This pioneer study on a simple volcanic fan aquifer system with a well-understood groundwater flow mechanism provides a useful model for future studies.
对雅加达盆地地下水溶解硫酸盐中的硫酸盐同位素比值(δ³⁴S(SO₄)和 δ¹⁸O(SO₄))进行测定,研究了含水层系统中硫酸盐的来源及其通过生物地球化学反应的形成/降解。地下水的流动路径、水龄和地球化学特征在前些年的研究中已有详细描述,为地下水化学和同位素数据提供了框架,这些数据还补充了盆地内泉水、河水、温泉水、海水、洗涤剂和肥料的数据。地下水样本的硫酸盐同位素组成变化范围很广,δ³⁴S(SO₄)为-2.9‰至+33.4‰,δ¹⁸O(SO₄)为+4.9‰至+17.8‰,并沿从北部山区到沿海地区的流向呈系统变化。地下水样本分为三组,分别具有(1)相对较低且狭窄的 δ(34)S(SO₄)(+2.3‰至+7.6‰)和较低且变化较大的 δ¹⁸O(SO₄)(+4.9‰至+12.9‰)组成,(2)较高且变化较大的 δ³⁴S(SO₄)(+10.2‰至+33.4‰)和较高的 δ¹⁸O(SO₄)(+12.4‰至+17.3‰)组成,以及(3)较低的 δ³⁴S(SO₄)(<+6.1‰)和较高的 δ¹⁸O(SO₄)(高达+17.8‰)组成。这三种类型的地下水分别存在于陆地无压含水层、沿海无压和承压含水层以及陆地承压含水层中。现场测量、浓度和以前确定的 δ¹⁵N(NO₃)数据的组合表明,观察到的同位素异质性主要是农村地区生活污水污染物、沿海地区经历过先前细菌硫酸盐还原的海水硫酸盐以及细菌元素硫歧化作用形成硫酸盐过程中同位素分馏的综合结果。我们的结果清楚地支持这样一种假设,即人类活动是理解现代地下环境硫循环的重要因素。由于复杂的水文地质研究背景导致同位素比值各不相同,因此很少提出沿地下水流动的硫酸盐同位素演化的一般模型,尽管最近人们对其有了很大的关注。这项对具有良好地下水流动机制的简单火山扇含水层系统的开创性研究为未来的研究提供了一个有用的模型。