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151 - Prevalence of Arsenic Enrichment Near the Sediment-Water<br />

Interface Along Shorelines of the Great Lakes<br />

Sabina Rakhimbekova, Clare Robinson, & Denis O’Carroll<br />

Department of Civil and Environmental Engineering – University of Western Ontario,<br />

London, Ontario, Canada<br />

The mobility of arsenic in groundwater is controlled by interacting biogeochemical and<br />

hydrological processes – these processes are complicated near surface water-groundwater<br />

interfaces due to the mixing of two distinct water entities. The mixing of anoxic groundwater<br />

with toxic lake water recirculating across the sediment-water interface sets up a reaction<br />

zone characterized by sharp pH and redox gradients where a range of chemicals (e.g.,<br />

arsenic) undergo important transformations. While prior research has revealed arsenic<br />

enrichment near the sediment-water interface along the shores of the Great Lakes (up<br />

to 56 µg/L), there is limited understanding of the ultimate source of arsenic, the physical<br />

and geochemical processes governing the arsenic behaviour and if arsenic enrichment in<br />

beach aquifers is a naturally occurring widespread phenomenon. This paper presents pore<br />

water and sediment chemistry data obtained near the sediment-water interface at a wide<br />

range of permeable Great Lake shorelines. Elevated As concentrations at a number of field<br />

sites indicates the process may be naturally occurring and suggests that lake water with<br />

trace concentrations of arsenic may deliver arsenic to the beach aquifer as it recirculates<br />

across the sediment-water interface. Arsenic may then be sequestered by metal oxides that<br />

precipitate below the beach face in distinct redox zones. The accumulation of arsenic in<br />

the beach aquifer creates a potential risk of elevated arsenic concentrations being rapidly<br />

released back to the surface water under favorable hydrologic and geochemical conditions<br />

(e.g., high organic loading from algae washup). The paper also explores potential scenarios<br />

that may cause mobilization of arsenic from the aquifer and subsequent release to adjacent<br />

surface waters.<br />

152 - Quantification of groundwater discharge along shorelines of<br />

the Great Lakes using Radon-222<br />

Tao Ji & Clare Robinson<br />

Department of Civil and Environmental Engineering – Western University, London,<br />

Ontario, Canada<br />

Groundwater discharge can be a significant pathway for transporting pollutants, including<br />

nutrients, organic contaminants and trace metals, into nearshore waters of the Great<br />

Lakes. Groundwater as a contributor of nutrients to the Great Lakes has received increased<br />

attention in recent years, particularly with respect to the potential for onsite sewage<br />

systems to be a source of elevated nutrient levels in nearshore waters. There is, however,<br />

limited understanding and methods available to quantify the groundwater discharge to the<br />

Great Lakes, including regional-scale methods to identify hotspot areas of discharge. Radon<br />

( 222 Rn, t 1/2<br />

= 3.8 days) is a suitable natural tracer for estimating groundwater discharge<br />

because it is a conservative gas and its activity is typically 3-4 orders of magnitude higher<br />

in groundwater than in surface water. Regional-scale 222 Rn surveys were conducted along<br />

160 IAH-CNC 2015 WATERLOO CONFERENCE

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