Hillslope soil water flowpaths and the dynamics of roadside soil cation pools influenced by road deicers. Issue 1 (10th October 2016)

• Record Type: Journal Article
• Authors: Rossi, Robert J.; Bain, Daniel J.; Elliott, Emily M.; Divers, Marion; O'Neill, Bridget
• Is Part Of: Hydrological processes. Volume 31:Issue 1(2017)
• Page Start: 177
• Page End: 190
• Publication Date: 2016-10-10
• Subjects: road salt -- roadside soil -- hillslope hydrology -- potassium -- magnesium -- calcium; Hydrology -- Periodicals; Hydrology -- Research -- Periodicals; Hydrologic models -- Periodicals; Hydrological forecasting -- Periodicals; 631.432
• DOI: 10.1002/hyp.10989
• Languages: English
• ISSNs: 0885-6087

Abstract

Abstract: Over the past 60 years, road deicers (i.e. road salt) have been applied to roadways in high latitudes to improve road conditions in winter weather. However, the dissolution of road deicers in highway runoff creates waters with high concentrations of sodium, which can mobilize soil metals via soil cation‐exchange reactions. While several studies have detailed the interactions of road salt‐rich solutions and surface and ground waters, less attention has been given to how local hydrologic flowpaths can impact the delivery of these solutions to near‐road soils. Between 2013 and 2014, soil water samples were collected from a roadside transect of lysimeter nests in Pittsburgh, Pennsylvania (USA). Soil water samples were analysed for metal concentrations and resulting data used to examine cation dynamics. While patterns in soil water calcium and magnesium concentrations follow patterns in soil water sodium concentrations, additional processes influence patterns in soil water potassium concentrations. Specifically, we observe the highest calcium and magnesium concentrations in the deepest lysimeters, suggesting divalent cations are mobilized to, and potentially accumulate in, deeper soil horizons. In contrast, soil water potassium concentrations do not follow this pattern. Additionally, in all examined elements (Ca, Mg, K, Na, and Cl), the timing of concentration peaks appears be influenced by a combination of both distance from the roadside and sampling depth. These relationships not only suggest that multiple soil water flowpaths interact with our study transect but also confirm that road salt plumes persist and migrate following the road salting season. Characterizing the interactions of sodium‐rich solutions and roadside soil cation pools clarifies our understanding of metal dynamics in the roadside environment. A deeper understanding of these processes is necessary to effectively restore and manage watersheds as high total dissolved solid solutions (e.g. road deicing melt, unconventional natural gas brines, and marginal irrigation water) continue to influence hydrological systems. Copyright © 2016 John Wiley & Sons, Ltd.