Long-Term Annual and Seasonal Patterns of Acidic Deposition and Stream Water Quality in a Great Smoky Mountains High-Elevation Watershed

被引:19
作者
Cai, Meijun [1 ]
Schwartz, John S. [1 ]
Robinson, R. Bruce [1 ]
Moore, Stephen E. [2 ]
Kulp, Matt A. [2 ]
机构
[1] Univ Tennessee, Dept Civil & Environm Engn, Knoxville, TN 37996 USA
[2] US Dept Interior, Natl Pk Serv, Gatlinburg, TN 37738 USA
关键词
Acidic deposition; Stream acidification; temporal trends; Seasonal variation; Water quality; Climate change; Southern Appalachian; SHENANDOAH-NATIONAL-PARK; NEW-YORK; UNITED-STATES; ADIRONDACK REGION; ATMOSPHERIC DEPOSITION; FORESTED WATERSHEDS; NITROGEN DEPOSITION; FRESH-WATERS; CHEMISTRY; TRENDS;
D O I
10.1007/s11270-010-0727-z
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The recovery potential of stream acidification from years of acidic deposition is dependent on biogeochemical processes and varies among different acid-sensitive regions. Studies that investigate long-term trends and seasonal variability of stream chemistry in the context of atmospheric deposition and watershed setting provide crucial assessments on governing biogeochemical processes. In this study, water chemistries were investigated in Noland Divide watershed (NDW), a high-elevation watershed in the Great Smoky Mountains National Park (GRSM) of the southern Appalachian region. Monitoring data from 1991 to 2007 for deposition and stream water chemistries were statistically analyzed for long-term trends and seasonal patterns by using Seasonal Kendall Tau tests. Precipitation declined over this study period, where throughfall (TF) declined significantly by 5.76 cm year(-1). Precipitation patterns play a key role in the fate and transport of acid pollutants. On a monthly volume-weighted basis, pH of TF and wet deposition, and stream water did not significantly change over time remaining around 4.3, 4.7, and 5.8, respectively. Per NDW area, TF SO4 (2-) flux declined 356.16 eq year(-1) and SO4 (2-) concentrations did not change significantly over time. Stream SO4 (2-) remained about 30 mu eq L-1 exhibiting no long-term trends or seasonal patterns. SO4 (2-) retention was generally greater during drier months. TF monthly volume-weighted NH4 (+) and NO3 (-) concentrations significantly increased by 0.80 mu eq L-1 year(-1) and 1.24 mu eq L-1 year(-1), respectively. TF NH4 (+) fluxes increased by 95.76 eq year(-1). Most of NH4 (+) was retained in the watershed, and NO3 (-) retention was much lower than NH4 (+). Stream monthly volume-weighted NO3 (-) concentrations and fluxes significantly declined by 0.56 mu eq L-1 year(-1) and 139.56 eq year(-1), respectively. Overall, in NDW, inorganic nitrogen was exported before 1999 and retained since then, presumably from forest regrowth after Frazer fir die-off in the 1970s from balsam wooly adelgid infestation. Stream export of NO3 (-) was greater during winter than summer months. During the period from 1999 to 2007, stream base cations did not exhibit significant changes, apparently regulated by soil supply. Statistical models predicting stream pH, ANC, SO4 (2-), and NO3 (-) concentrations were largely correlated with stream discharge and number of dry days between precipitation events and SO4 (2-) deposition. Dependent on precipitation, governing biogeochemical processes in NDW appear to be SO4 (2-) adsorption, nitrification, and NO3 (-) forest uptake. This study provided essential information to aid the GRSM management for developing predictive models of the future water quality and potential impacts from climate change.
引用
收藏
页码:547 / 562
页数:16
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