U.S. Geological Survey, Ohio-Kentucky-Indiana Water Science Center, Louisville, KY, USA.
Lewis Honors College, University of Kentucky, Lexington, KY, USA.
J Environ Manage. 2023 Apr 15;332:117392. doi: 10.1016/j.jenvman.2023.117392. Epub 2023 Feb 3.
Hydrologic monitoring began on two headwater streams (<1 km) on the University of Kentucky's Robinson Forest in 1971. We evaluated stream-water (1974-2013) and bulk-deposition (wet + dust) (1984-2013) chemistry in the context of regional wet-deposition patterns that showed decreases in both sulfate and nitrate concentrations as well as proximal surface-mine expansion. Decadal time steps (1974-83, 1984-93, 1994-2003, 2004-2013) were used to quantify change. Comparison of the first two decades showed similarly decreased sulfate (minimum flow-adjusted annual-mean concentration of ≈13.5 mg/L in 1982 to 8.8 mg/L in 1992) and increased pH (6.6-6.8) in both streams, reflecting contemporaneous changes in both bulk and wet deposition. In contrast, concentrations of nitrate (0.14 to >0.25 mg/L) and base cations increased between these two decades, coinciding with expansion of surface mining between 1985 and 1995. In 2004, stream-water pH (6.7 in 2004), sulfate (9.2 mg/L), and nitrate (>0.11 mg/L) were similar to 1982, despite wet-deposition concentrations being lower. Base-cation concentrations were higher in the stream adjacent to ongoing surface mining relative to the stream situated near the middle of the experimental forest. However, pH decreased to approximately 5.7 by 2013 for both streams, which, combined with a shift in dominant cations from calcium to magnesium and potassium, indicates that the soil-buffering capacity of this landscape has been exceeded. Ratios of bulk deposition and stream-water concentrations indicate enrichment of sulfate (1.7-25.2) and cations (0.5-64.8), but not nitrogen (0.1-5.6), indicating that the Forest is not nitrogen saturated and that ongoing changes in water-quality are sulfate driven. When concentrations were adjusted to account for changes in streamflow (climate) over the 4 decades, external influences (land management/regulation) explained most change. The amount and direction of change differed among constituents, both between consecutive decades and between the first and last decades, reflecting the influence of localized surface mining even as regional wet deposition continued to improve due to the Clean Air Act. The implication is that localized stressors have the potential to out-pace the benefits of national environmental policies for communities that depend on local water-resources in similar environments.
1971 年,肯塔基大学罗宾逊森林开始对两条(<1 公里)的源头溪流进行水文监测。我们评估了溪流水质(1974-2013 年)和整体沉降(湿沉降+降尘)(1984-2013 年)的化学性质,其中包括区域湿沉降模式,该模式显示硫酸盐和硝酸盐浓度都降低了,而且附近的露天矿也在扩张。我们使用十年时间步长(1974-83 年、1984-93 年、1994-2003 年、2004-2013 年)来量化变化。前两个十年的比较显示,两条溪流中的硫酸盐(最小流量调整后的年平均浓度在 1982 年约为 13.5mg/L,在 1992 年降至 8.8mg/L)和 pH 值(6.6-6.8)均呈相似下降趋势,反映出同期的整体和湿沉降变化。相比之下,硝酸盐(0.14 至>0.25mg/L)和碱金属阳离子的浓度在这两个十年之间增加,这与 1985 年至 1995 年期间露天矿的扩张相吻合。尽管湿沉降浓度较低,但 2004 年溪流的 pH 值(2004 年为 6.7)、硫酸盐(9.2mg/L)和硝酸盐(>0.11mg/L)与 1982 年相似。与位于实验林中部附近的溪流相比,靠近正在进行的露天矿的溪流中碱金属阳离子的浓度更高。然而,到 2013 年,两条溪流的 pH 值都下降到了大约 5.7,这表明该景观的土壤缓冲能力已经超过了这个水平。整体沉降和溪流水质浓度的比值表明硫酸盐(1.7-25.2)和阳离子(0.5-64.8)的富集,但氮(0.1-5.6)没有,这表明森林没有氮饱和,水质的持续变化是由硫酸盐驱动的。当考虑 40 年来溪流流量(气候)变化对浓度的影响时,外部影响(土地管理/法规)解释了大部分变化。不同组成部分之间,无论是连续十年之间还是前十年和最后十年之间,变化的幅度和方向都不同,这反映了局部露天矿的影响,尽管由于《清洁空气法案》,区域湿沉降仍在继续改善。这意味着,对于依赖类似环境中当地水资源的社区来说,局部压力源有可能超过国家环境政策的好处。