Buffam Ishi, Laudon Hjalmar, Seibert Jan, Mörth Carl-Magnus, Bishop Kevin
Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
Sci Total Environ. 2008 Dec 15;407(1):708-22. doi: 10.1016/j.scitotenv.2008.10.006. Epub 2008 Oct 21.
Spatial and temporal patterns in streamwater acidity are ecologically important, but difficult to measure in parallel. Here we present the spatial distribution of streamwater chemistry relevant to acidity from 60 stream sites distributed throughout a 67 km2 boreal catchment, sampled during a period of winter baseflow (high pH) and during a spring flood episode (low pH). Sites were grouped based on pH level and pH change from winter baseflow to spring flood. The site attributes of each pH group were then assessed in terms of both stream chemistry and subcatchment landscape characteristics. Winter baseflow pH was high throughout most of the stream network (median pH 6.4), but during the spring flood episode stream sites experienced declines in pH ranging from 0-1.6 pH units, resulting in pH ranging from 4.3-6.3. Spring flood pH was highest in larger, lower altitude catchments underlain by fine sorted sediments, and lowest in small, higher altitude catchments with a mixture of peat wetlands and forested till. Wetland-dominated headwater catchments had low but stable pH, while the spring flood pH drop was largest in a group of catchments of intermediate size which contained well-developed coniferous forest and a moderate proportion of peat wetlands. There was a trend with distance downstream of higher pH, acid neutralizing capacity (ANC) and base cation concentrations together with lower dissolved organic carbon (DOC, strongly negatively correlated with pH). This apparent scale-dependence of stream chemistry could be explained by a number of environmental factors which vary predictably with altitude, catchment area and distance downstream--most notably, a shift in surficial sediment type from unsorted till and peat wetlands to fine sorted sediments at lower altitudes in this catchment. As a result of the combination of spatial heterogeneity in landscape characteristics and scale-related processes, boreal catchments like this one can be expected to experience high spatial variability both in terms of chemistry at any given point in time, and in the change experienced during high discharge episodes. Although chemistry patterns showed associations with landscape characteristics, considerable additional variability remained, suggesting that the modeling of dynamic stream chemistry from map parameters will continue to present a challenge.
河流水酸度的时空模式具有重要的生态意义,但难以同时进行测量。在此,我们展示了来自一个面积为67平方公里的北方集水区内60个溪流站点的与酸度相关的河流水化学空间分布情况,这些样本采集于冬季基流期(高pH值)和春季洪水期(低pH值)。站点根据pH值水平以及从冬季基流到春季洪水期间的pH值变化进行分组。然后,从河流水化学和子集水区景观特征两方面对每个pH值组的站点属性进行评估。冬季基流期间,大部分溪流网络的pH值较高(中位数pH值为6.4),但在春季洪水期,溪流站点的pH值下降了0 - 1.6个pH单位,导致pH值范围为4.3 - 6.3。春季洪水期的pH值在由细粒沉积物覆盖的较大、较低海拔集水区最高,而在泥炭湿地和森林化冰碛混合的小、较高海拔集水区最低。以湿地为主的源头集水区pH值较低但稳定,而春季洪水期pH值下降幅度最大的是一组中等规模的集水区,这些集水区包含发育良好的针叶林和一定比例的泥炭湿地。随着下游距离的增加,pH值、酸中和能力(ANC)和碱金属阳离子浓度呈上升趋势,而溶解有机碳(DOC,与pH值呈强烈负相关)呈下降趋势。这种明显的河流水化学尺度依赖性可以由一些随海拔、集水区面积和下游距离可预测变化的环境因素来解释——最显著的是,在该集水区较低海拔处,表层沉积物类型从无分选的冰碛和泥炭湿地转变为细粒沉积物。由于景观特征的空间异质性和与尺度相关的过程相互结合,像这样的北方集水区在任何给定时间点的化学性质以及在高流量期所经历的变化方面,预计都会有很高的空间变异性。尽管化学模式显示出与景观特征有关联,但仍存在相当大的额外变异性,这表明根据地图参数对动态河流水化学进行建模将继续是一项挑战。