Abstracts
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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