“…Arsenic is a globally recognized geogenic and anthropogenic metalloid contaminant, − for which little information is available in a permafrost context. ,, Outside permafrost regions, it occurs in the oxidation states As(−I), As(III), and As(V) . Arsenite [As(III)] and arsenate [As(V)] are the dominant species encountered, although As(−I) sulfides and thiolated and methylated As(III) and As(V) species also occur under sulfidic and methanogenic redox conditions. ,− Iron-(oxyhydr)oxides are major solid-phase hosts of arsenite and arsenate in soils and sediments. ,, These phases are typically encountered at μg g –1 levels in alluvial materials because oxidizing conditions encountered during weathering and transport in surface water bodies favor their stability and transfer to depositional areas. ,, Iron-(oxyhydr)oxides exhibit high affinity toward As, forming stable inner and outer-sphere complexes with arsenite and arsenate. ,− However, their exposure to reducing conditions, encountered during rising subsurface water levels and/or exposure to labile organic C, triggers As mobilization via reductive dissolution. − This process is recognized worldwide as a driver of geogenic As release in aquifers composed of unconsolidated sediments across geologic environments and climatic conditions. ,,,− …”