STREAM WATER CHEMISTRY IN WATERSHEDS RECEIVING DIFFERENT ATMOSPHERIC INPUTS OF H+, NH4, NO3−, AND SO42−1

ABSTRACT: Weekly precipitation and stream water samples were collected from small watersheds in Denali National Park, Alaska, the Fraser Experimental Forest, Colorado, Isle Royale National Park, Michigan, and the Calumet watershed on the south shore of Lake Superior, Michigan. The objective was to determine if stream water chemistry at the mouth and upstream stations reflected precipitation chemistry across a range of atmospheric inputs of H⁺, NH₄⁺, NO₃^?_?, and SO₄^2?. Volume-weighted precipitation H⁺, NH₄⁺, NO₃^?_?, and SO₄^2? concentrations varied 4 to 8 fold with concentrations highest at Calumet and lowest in Denali. Stream water chemistry varied among sites, but did not reflect precipitation chemistry. The Denali watershed, Rock Creek, had the lowest precipitation NO₃^?_? and SO₄^2? concentrations, but the highest stream water NO₃^?and SO₄^2? concentrations. Among sites, the ratio of mean monthly upstream NO₃^?_? concentration to precipitation NO₃^?_- concentration declined (p < 0.001, R²= 0.47) as precipitation NO₃^?_? concentration increased. The ratio of mean monthly upstream to precipitation SO₄^2? concentration showed no significant relationship to change in precipitation SO₄^2? concentration. Watersheds showed strong retention of inorganic N (> 90 percent inputs) across inputs ranging from 0.12 to > 6 kg N ha^?1 y^?1. Factors possibly accounting for the weak or non-existent signal between stream water and precipitation ion concentrations include rapid modification of meltwater and precipitation chemistry by soil processes, and the presence of unfrozen soils which permits winter mineralization and nitrification to occur.