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Abstract Synoptic sampling of streams is an inexpensive way to gain insight into the spatial distribution of dissolved constituents in the subsurface critical zone. Few spatial synoptics have focused on urban watersheds although this approach is useful in urban areas where monitoring wells are uncommon. Baseflow stream sampling was used to quantify spatial variability of water chemistry in a highly developed Piedmont watershed in suburban Baltimore, MD having no permitted point discharges. Six synoptic surveys were conducted from 2014 to 2016 after an average of 10 days of no rain, when stream discharge was composed of baseflow from groundwater. Samples collected every 50 m over 5 km were analyzed for nitrate, sulfate, chloride, fluoride, and water stable isotopes. Longitudinal spatial patterns differed across constituents for each survey, but the pattern for each constituent varied little across synoptics. Results suggest a spatially heterogeneous, three‐dimensional pattern of localized groundwater contaminant zones steadily contributing solutes to the stream network, where high concentrations result from current and legacy land use practices. By contrast, observations from 35 point piezometers indicate that sparse groundwater measurements are not a good predictor of baseflow stream chemistry in this geologic setting. Cross‐covariance analysis of stream solute concentrations with groundwater model/backward particle tracking results suggest that spatial changes in base‐flow solute concentrations are associated with urban features such as impervious surface area, fill, and leaking potable water and sanitary sewer pipes. Predicted subsurface residence times suggest that legacy solute sources drive baseflow stream chemistry in the urban critical zone.
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Where the past meets the present: connecting nitrogen from watersheds to streams through groundwater flowpaths
Abstract Groundwater discharge to streams is a nonpoint source of nitrogen (N) that confounds N mitigation efforts and represents a significant portion of the annual N loading to watersheds. However, we lack an understanding of where and how much groundwater N enters streams and watersheds. Nitrogen concentrations at the end of groundwater flowpaths are the culmination of biogeochemical and physical processes from the contributing land area where groundwater recharges, within the aquifer system, and in the near-stream riparian area where groundwater discharges to streams. Our research objectives were to quantify the spatial distribution of N concentrations at groundwater discharges throughout a mixed land-use watershed and to evaluate how relationships among contributing and riparian land cover, modeled aquifer characteristics, and groundwater discharge biogeochemistry explain the spatial variation in groundwater discharge N concentrations. We accomplished this by integrating high-resolution thermal infrared surveys to locate groundwater discharge, biogeochemical sampling of groundwater, and a particle tracking model that links groundwater discharge locations to their contributing area land cover. Groundwater N loading from groundwater discharges within the watershed varied substantially between and within streambank groundwater discharge features. Groundwater nitrate concentrations were spatially heterogeneous ranging from below 0.03–11.45 mg-N/L, varying up to 20-fold within meters. When combined with the particle tracking model results and land cover metrics, we found that groundwater discharge nitrate concentrations were best predicted by a linear mixed-effect model that explained over 60% of the variation in nitrate concentrations, including aquifer chemistry (dissolved oxygen, Cl−, SO42−), riparian area forested land cover, and modeled physical aquifer characteristics (discharge, Euclidean distance). Our work highlights the significant spatial variability in groundwater discharge nitrate concentrations within mixed land-use watersheds and the need to understand groundwater N processing across the many spatiotemporal scales within groundwater cycling.
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- Award ID(s):
- 1824820
- PAR ID:
- 10478245
- Publisher / Repository:
- IOP
- Date Published:
- Journal Name:
- Environmental Research Letters
- Volume:
- 18
- Issue:
- 12
- ISSN:
- 1748-9326
- Page Range / eLocation ID:
- 124039
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1088/1748-9326/ad0c86
