JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org. This content downloaded from 134.114.138.130 on Tue, 30 Jun 2015 20:35:02 UTC All use subject to JSTOR Terms and ConditionsAbstract. Watershed studies across the northeastern United States have shown that stream losses of S042-exceed atmospheric sulfur (S) deposition. Understanding the processes responsible for this additional source of S is critical to quantifying ecosystem response to ongoing and potential future controls on SO2 emission. An integrated biogeochemical model, PnET-BGC, was used to investigate inputs and dynamics of S in a northern hardwood forest at the Hubbard Brook Experimental Forest (HBEF), New Hampshire, USA. The changes in soil S pools and stream-water S042-were simulated to assess the response to both atmospheric S deposition and forest clear-cutting disturbances. Model simulation using the measured dry-to-bulk deposition ratio of 0.21 resulted in an underprediction of soil S pools and stream-water S042-concentrations in the biogeochemical reference watershed (Watershed 6). However, the depiction of biotic processes (e.g., plant uptake, mineralization) in the model reduced the discrepancy in stream SO42-concentration between measured and model predicted value by -50% compared to a previous modeling effort that only considered abiotic processes.
Long-term simulations (-150 yr) indicated that elevated anthropogenic S deposition has increased stream S042-concentrations and enhanced the incorporation of S in adsorbed S042-and organic S soil pools. Following the implementation of the 1970 and 1990 Amendments to the Clean Air Act, decreases in S deposition resulted in the net release of S from soil pools, including soil organic S. Model simulation of forest clear-cutting of Watershed 5 at the HBEF showed that NO3-leachingand associated acidification following this disturbance increased adsorption of SO42-to soil. Compared to the reference watershed, stream-water SO42-concentrations were slightly higher, and soil adsorbed SO42-pools were substantially higher in the clear-cut watershed 4-5 yr after disturbance. Simulation of stable S isotopes showed that fractionation associated with the mineralization of soil organic S might explain the depletion in 34S observed between throughfall and stream water in the reference watershed. There is a need for further research on: (1) the rates of dry S deposition and (2) the rate of weathering of various minerals and the isotopic composition of these minerals in order to fully assess the discrepancy (i.e., greater export of S than can be accounted for by atmospheric deposition) in watershed S mass balances. The results of forecasts of the future response to anticipated decreases in S deposition are highly dependent on the natur...