Coupled biogeochemical cycles in riparian zones with contrasting hydrogeomorphic characteristics in the US Midwest

Abstract

Numerous studies have investigated the fate of pollutants in riparian buffers, but few studies have focused on the control of multiple contaminants simultaneously in riparian zones. To better understand what drives the biogeochemical cycles of multiple contaminants in riparian zones, a 19-month study was conducted in riparian buffers across a range of hydrogeomorphic (HGM) settings in the White River watershed in Indiana. Three research sites [Leary Webber Ditch (LWD), Scott Starling (SS) and White River (WR)] with contrasting hydro-geomorphology were selected. We monitored groundwater table depth, oxidation reduction potential (ORP), dissolved oxygen (DO), dissolved organic carbon (DOC), NO3-, NH4+, soluble reactive phosphorus (SRP), SO42- , total Hg and methylmercury (MeHg). Our results revealed that differences in HGM conditions translated into distinctive site hydrology, but significant differences in site hydrology did not lead to different biogeochemical conditions. Nitrate reduction and sulfate re-oxidation were likely associated with major hydrological events, while sulfate reduction, ammonia and methylmercury production were likely associated with seasonal changes in biogeochemical conditions. Results also suggest that the LWD site was a small sink for nitrate but a source for sulfate and MeHg, the SS site was a small sink for MeHg but had little effect on NO3-, SO42- and SRP, and the WR was an intermediate to a large sink for nitrate, an intermediate sink for SRP, and a small source for MeHg. Land use and point source appears to have played an important role in regulating solute concentrations (NO3-, SRP and THg). Thermodynamic theories probably oversimplify the complex patterns of solute dynamics which, at the sites monitored in the present study, were more strongly impacted by HGM settings, land use, and proximity to a point source.