The physical (water quantity) and chemical (water quality) conditions of aquatic ecosystems in the oil sands region are driven by both natural processes (e.g., atmospheric deposition, runoff, erosion, groundwater flow) and human activities (e.g., contaminant inputs deposited on land, snow cover, or water; alterations to natural landscapes and water flow). Under pre- and post-industrial conditions, natural bitumen in the McMurray Formation (the minable oil sands deposit,
Fig. 1) is physically eroded and transported principally by river scour or flow. Under conditions of industrial mining and bitumen processing, the Province of Alberta has mandated a zero release of oil sand process water and sediments to natural river system. While there are circumstances where small releases have been approved by the regulator (
RAMP 2015,
2016), they represent less than 1% of receiving river flows. Moreover, although leakage of process water from tailings ponds is known to impact groundwater (
Fennell and Arciszewski 2019), there is limited potential for subsequent transport and discharge to nearby rivers (
CEC 2020), and any groundwater seepage reaching the river is rapidly diluted (
Ferguson et al. 2009;
Gibson et al. 2013;
Sun et al. 2017;
Roy et al. 2016;
CEC 2020). As such, the release of contaminants from industrial processes to aquatic ecosystems is currently principally confined to atmospheric release and transport of stack emissions, as well as fugitive dust from open and bare lease areas (e.g., open pits, surface material storage areas, roads, etc.) susceptible to wind entrainment of dust and associated contaminants (
Kirk et al. 2014;
2018;
Brook et al. 2019). A key component of this dust, pet coke, is of particular concern due to high levels of polycyclic aromatic compounds (PACs) and metals such as vanadium (V) (
Zhang et al. 2016). Particulate emissions, in part, deposit on the landscape and to the snowpack and are then transported to adjacent water courses during snowmelt and precipitation events (
Kelly et al. 2009,
2010;
Kirk et al. 2014;
Gopalapillai et al. 2019;
Wasiuta et al. 2019;
Chibwe et al. 2020). Given that river and lake surfaces represent a fraction of the total surface area in the oil sands region, direct atmospheric deposition to water and ice should be small relative to deposition to land surfaces and snowpack. The surface transport of contaminants via washoff and snowmelt will depend on soil state (e.g., whether frozen or not, and organic carbon content), vegetation cover, and topography. It should be recognized, however, that atmospherically deposited contaminants will accumulate in the soils over long periods of time (particularly when the ground is not frozen) and may represent a large non-point source should an extreme event cause mass erosion over a large surface area. Regardless, contaminants do accumulate in lake and river sediments; however, the lag time in delivery is uncertain (
Evans et al. 2016;
Emmerton et al. 2018).
Most atmospheric deposition occurs within 30 km of the source as there is a rapid drop-off in deposited compounds (e.g., PACs, mercury (Hg)) with distance from surface mining source (
Kelly et al. 2009;
Kirk et al. 2014;
Harner et al. 2018). Catchment-scale snowpack Hg and methylmercury (MeHg) loads, normalized to watershed area, were found to be highest near oil sands operations, and river water Hg concentrations and loads followed seasonal discharge patterns and tended to be higher downstream of mining operations. Aerial loadings of Hg and MeHg to tributary catchments equaled or exceeded the mass of Hg and MeHg exported during freshet and, in some cases, the entire hydrologic year. In addition, during years of high discharge, these low-relief systems appear to become connected and flush MeHg (and Hg) from the watershed (
Wasiuta et al. 2019). Runoff of aerially deposited particles from both land and snow cover is controlled by hillslope angle, extent and type of vegetation, degree of frozen ground, canopy capture, etc., with much of the particulate deposition trapped, stored, and unavailable for river transport until hydrological conditions allow for flushing of contaminants from storage (
Droppo et al. 2018a,
2019;
Wasiuta et al. 2019). The potential for dissolution, infiltration, and shallow groundwater transport of particulate-derived contaminants to nearby rivers is uncertain, but the presence of soil organic matter would be expected to attenuate the transport of such organic compounds dissolved from airborne deposition to a large extent, though this process likely varies among years.