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Pollutant Drivers

Authored By: P. G. Schaberg, E. K. Miller, C. Eagar

Through industrial activity and the increased combustion of fossil fuels over the past century, humans have dramatically increased gaseous emissions of sulfur dioxide (SO2), nitrogen oxides (NOx), and ammonia (NH3) and particulate emissions of acidifying compounds (Driscoll and others 2001). Recent pollution controls have reduced emissions of sulfur (S) -based compounds in Europe and North America, resulting in moderate reductions in S deposition, but there has been little change in nitrogen (N) deposition (Driscoll and others 2001, UNECE 2005). In contrast to North America and Europe, with rapid economic development and economic growth Asia— and most notably China—have significantly increased fossil fuel combustion in recent years (Liu and Diamond 2005). As a result, emissions of SO2, NOx,, NH3, and associated compounds have increased greatly in the region (Carmichael and others 2002, Liu and Diamond 2005, Richter and others 2005). In fact, pollutant deposition of S and N compounds now affects a quarter of China’s land area, making China one of the countries most affected by these pollutants (Feng and others 2002, Jianguo and Diamond 2005).

Through the atmospheric conversions of SO2 and NOx to the acids H2SO4 and HNO3, as well as the release of H+ during the oxidation of NH4+ by soil microbes, S- and N-based pollutants act to acidify forest systems (Driscoll and others 2001). Among other impacts, this acidification increases the leaching of base cations from soils ( Kirchner and Lydersen 1995, Likens and others 1996, Likens and others 1998, Schulze 1989), and enhances the availability of aluminum (Al), which reduces base cation availability for plant uptake (Cronan and Scholield 1990, Lawrence and others 1995). In addition to the atmospheric production of acids from pollutant constituents, N inputs can lead to N saturation (the availability of N in excess of biological demand), which can deplete cations as excess N leaches from forest soils (Aber and others 1998). It has even been hypothesized that pollution-associated climatic warming could enhance rates of natural acidifying process, further exacerbating soil cation loss (Tomlinson 1993). In addition to pollution-associated cation loss, a side effect of existing pollution controls has been the reduced emission of particulates that contain base cations such as Ca (Hedin and others 1994). Reduced inputs and increased removals of cations from forests have resulted in net depletions that have been documented in a variety of ways, including long-term changes in stream chemistry, the analysis of archived soils, and the chemical analysis of tree xylem cores.


Click to hide citations... Literature Cited
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  • Cronan, C.S.; Scholield, C.L. 1990. Relationships between aqueous aluminum and acidic deposition in forested watersheds of North America and Northern Europe. Environmental Science and Technology. 24: 1100-1105.
  • Driscoll, C.T.; Lawerence, G.B.; Bulger, A.J.; [and others]. 2001. Acidic deposition in the northeastern United States: Sources and inputs, ecosystem effects, and management strategies. BioScience. 51: 180-198.
  • Feng, Z.; Miao, H.; Zhang, F.; Huang, Y. 2002. Effects of acid deposition on terrestrial ecosystems and their rehabilitation strategies in China. Journal of Environmental Science. 14: 227-233.
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Encyclopedia ID: p3178



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