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Soil Solution Chemical Response to Two Decades of Experimental Acidification at the Bear Brook Watershed in Maine
Authors:Farrah R Fatemi  Ivan J Fernandez  Johanna Szillery  Stephen A Norton  Lindsey E Rustad
Institution:1. Department of Geography and the Environment, Villanova University, Villanova, PA, 19085, USA
2. School of Forest Resources and Climate Change Institute, University of Maine, Orono, ME, USA
3. S.W. Cole Engineering, Bangor, ME, USA
4. Department of Earth Sciences, University of Maine, Orono, ME, USA
5. USDA Forest Service, Durham, NH, USA
Abstract:We examined long-term changes in soil solution chemistry associated with experimental, whole watershed-acidification at the Bear Brook Watershed in Maine (BBWM). At BBWM, the West Bear (WB) watershed has been treated with bimonthly additions of ((NH4)2 SO4) since 1989. The adjacent East Bear (EB) watershed serves as a biogeochemical reference. Soil solution chemistry in the EB watershed was relatively stable from 1989?C2007, with the exception of declining SO4?CS concentrations associated with a progressive decline in SO4?CS deposition during this period. Soil solution chemistry in WB reflected a progressive change in acid-neutralization mechanisms from base cation buffering to Al buffering associated with treatment during this period. Total dissolved Al concentrations progressively increased over time and were ~4× higher in 2007 than in 1989. Treatment of WB was also associated with long-term increases in soil solution H+, SO4?CS, and NO3?CN, whereas soil solution dissolved organic carbon (DOC) was unresponsive to treatment. For solutes such as Ca, H+, and SO4?CS, changes in stream chemistry were generally parallel to changes in soil solution chemistry, indicating a close coupling of terrestrial and aquatic processes that regulate the chemistry of solutions in this first-order stream watershed. For other solutes such as Al and DOC, solute concentrations were higher in soil solutions compared with streams, suggesting that sorption and transformation processes along hydrologic flow-paths were important in regulating the chemistry of solutions and the transport of these solutes.
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